' ''it,\v,r i > ■'• ,1 ' ' ■• ' ; 'i^chnical '''\ Chemists' Handbook Lunge g'tate QlnllEge of AgticuUute At Q^otnell Inioecaitg atliata. S7. 9. 9Itbrarg Cornell University Library TP 151.L96 Technical chemists' handboolc.Tables and 3 1924 003 620 006 a Cornell University fj Library The original of this book is in the Cornell University Library. There are no known copyright restrictions in the United States on the use of the text. http://www.archive.org/details/cu31924003620006 TECHNICAL CHEMISTS' HANDBOOK technical Chemists' Handbook TA'BLES AND METHODS OF ANALYSIS FOR MANUFACTURERS OF INORGANIC CHEMICAL PRODUCTS BY GEOEGE LUNGE, Ph.D. PROFESSOR EMERITUS OF TECHNICAL CHEMISTRV IK THE FEDERAL TECHNICAL UNIVEBSITT, ZURICH HONORARY AND FOREIGN MEMBER OF THE CHEMICAL SOCIETY, LONDON, AND OF THE AMERICAN CHEMICAL SOCIETY DR.ING.(H.C.) of KARLSRUHE, ETC., ETC. SECOND EDITION, REVISED NEW YORK D. VAN NOSTRAND COMPANY TWENTY-FIVE PARK PLACE 1916 PREFACE The aim of The Technical Chemists' Handbook is to effect, as far as possible, the task of establishing uniformity among practical chemists, buyers and sellers, and analysts, in regard to both the numerical data employed in their work and the analytical methods used for the control of processes, and for the testing of the resulting products. In the preparation of this new edition, all the analytical factors have been recalculated on the basis of the atomic weights published by the International Committee for 1916. This has involved in exceedingly numerous cases changes of the data contained in the last edition, some of them of importance even for merely practical purposes. The tables of specific gravities and other tables have been selected from among the most recent and reliable determinations. In regard to the analytical methods, they are again chosen as before, on the principle that, as a rule, only one method should be given for each analytical operation, as well as for the pre- paration of standard solutions and for sampling the materials, in order to avoid discrepancies such as might arise should two or more methods be described. The method chosen should always, of course, be that which permits the greatest degree of accuracy possible that can be attained in a well-appointed works labora- tory by a properly trained chemist. In cases where there is a choice between equally accurate methods, that occupying least time or least apparatus, or which is already widely known and employed, has been preferred. Many new methods have accord- ingly had to be omitted, but in all cases such omissions have viii PREFACE been justified by means of a careful examination of the relative merits of the processes under consideration, and only such methods as were found thoroughly reliable have been included. Also, a considerable number of tables of specific gravities of solutions not previously worked out, or which were unsatis- factory, have been very carefully checked and extended. When necessary, reference is made to the more complete treatment of the subject matter in my larger treatise, published with the co-operation of Dr Charles A. Keane, under the title Techmicai Methods of Chemical Analysis, in three volumes of two parts each, in 1908-1914. This treatise is referred to in the text as Tech. Meth. The Authoe. Zurich, Jan. 1916. CONTENTS GENEKAL TABLES PAGE 2 Note on Temperatures aud Atomic Weights . Table 1 . International Atomic Weights ..... ,, 2. Symbols, Molecular Weights, and Percentage Composition of Com pounds which are important in the Inorganic Chemical Industries and in Technical Analysis .... „ 3. Factors for calculating Gravimetric Analyses . „ 4. Density and Litre Weights of Gases and Vapours ,, 5. Calculation of the c.c. read off in Gas-volumetric Analysis to milli grams of the substance required 6. Solubility of Salts . ,, 7. Solubility of other Salts at various Temperatures , , 8. Solubility of Gases in Water ,, 9. Specific Gravities of Solids ,, 10. Weight of Substances as Stored ,j 11. Specific Gravity of Liquids ... ,, 12. Specific Gravity and Percentage of Saturated Solutions ,, 13. Linear Expansion of Substances ..... ,, 14. Comparison of Thermometric Scales .... A. Celsius (Centigrade) Degrees as Units B. Fahrenheit Degrees as Dnits ,, 15. Conversion of Centigrade into Fahrenheit Degrees above 100, and vice versa ... ,, 16. Melting Points (Freezing Points) . n 17, Freezing Mixtures ... .32 ,, 18. Boiling Points . ... 33 ,, 19. High Temperatures as measured with Le Chatelier's Pyrometer . 35 ,, 20, I. Beduction of the Volume of Gases to a Temperature of 0° C. 36 II. Reduction of the Volume of Gases to a Pressure of 760 mm. . 42 ,, 21. Factors for reducing a given Volume of Gas to Normal Temperature and Pressure ....... 48 ,, 21a. Volumes of- Water at different Temperatures . . ' 51 ,, 22. Reduction of Water Pressure to Mercurial Pressure . 51 ,, 23. Tension of Aqueous Vapour between -20 and +118° C. . 52 ,, 24. Tension of Aqueous Vapour for Temperatures above +40° C, . . 53 25. Tension of Aqueous Vapour in Inches of Mercury from 1° to 100° F. . 55 ,, 26. Boiling Point of Water at different Barometric Pressures . 57 ,, 27. Specific Heats :— (a) Of Solids and Liquids ; (&) of Gases and Vapours . 57 „ 28. Heating Bfiects :— (a) Definitions ; (&) of Fuels ; (c) of Gases . . . 58 30 X CONTENTS PAGE Table 29. Air Compression ...... 59 30. Explosive Uixtares of Gases and Air . . 60 31. Properties of the Liquefied Gases found in Commerce 61 32. Electrical Units ..... .62 33. Electro-chemical Equivalents ..... 62 34. Mathematical Tables : Circumference and Area of Circles, Squares, Cubes, Square and Cube Roots . . 63 35. FormulsB for Mensuration of Areas and Solid Contents . 77 36. ■Weights and Measures of different Countries . 79 37. Beducing English to Metrical Weights and Measures, and vice versa S3 38. Weight of Sheet Metals . . 87 39. Coinage of different Countries 88 SPECIAL PAKT I. Fdel and Furnaces ;— A. Fuel.—1. Moisture; 2. Residual Coke; 3. Ash 93 4, Sulphur .... 94 5. Calorific Power ... . 95 B. F%r7iaces. — 1. Chimney Gases ; Orsat Apparatus 95 Checking the Working of E\imaces . . 97 2. Gas from Producers (Generators) . . 97 Estimation of Hydrogen by the Orsat-Lunge Apjferatus . 98 3. Speed of Draught ; Fletcher's Anemometer 99 Tables for using this . 100 Soger's Differential Anemometer 102 C. Temperature. — Pyrometers . . 102 Le Chatelier's Pyrometer . . . 103 Pyrometers for the Highest Temperatures 104 D. Feed-water for Stea/m-BoiUrSt etc. 104 1. Hard7iess.~-(a) Temporary . . 104 (6) Total ; (c) Besidue on Evaporation . 105 Estimation of the Reagents required for i^uifying Water 105 II, Sulphuric Acid Manufacture : — A. Bi'imstone. — 1. Moisture; 2. Bituminous Substances ; 3. Ashes 106 4. Arsenic. . . 106 5. Direct Estimation of Sulphur . ... 107 Specific Gravities of Solutions of Sulphur in Carbon Disulphide . 107 6. Selenium ; 7- Degree of Fineness . . 108 B. Sp&nt Oxide of Gas-works. See '* Coal-Gas" (p. 522) 108 C. Pyrites.~l. Moisture; 2. Sulphur 108 3. Copper . 109 4. Lead; 5. Zinc . 110 6. Carbonates; 7. Arsenic 111 D. Burnt Pyrites (Cinders).—!. Sulphur 111 2. Copper; 3. Iron ... 112 E. Zino Blende.— 1. Total Sulphur ; 2. Zinc 112 3. Lead; 4. Lime and Magnesia ; 5. Arsenic. 114 ti. Carbonic Dioxide ; 7. Available Sulphur . 114 F. Cinders from Blende.— 1. Sulphur . 114 2. Zinc . . 115 CONTENTS xi II. Sulphuric Acid Mamufagtube— Co»£mue(2 : — paob 6. Gases: (I.) Chamber Process.— I. Burner Gases: (a) Estimation of SO2 by Reich's Test . . . 115 (b) Total Acids . . . . 116 2. Chamber Gases ....... IIC 3. Chamber Exit Gases : (a) Oxygen ; (p) Sulphur and Nitrogen Acida ... . ... 117 (c) Nitric Oxide ....... 119 (II.) Contact Process.— 1. The Entering Gases; 2. The Catalysed H. Sulphuric Acid ..... . . 120 1. Specific Gravities of Sulphuric Acid ; General Remarks . 120 Tables.— Specific Gravity of Sulphuric Acid at 60° P. 121 2. Table for reducing the Specific Gravities of Sulphuric Acid to any other Temperature . . . . . .126 3. Speciflc Gravities of Commercial Nordhausen Oil of Vitriol . 130 4. Specific Gravities and Percentage of Fuming Nordhausen Oil of Vitriol at different Temperatures ... 181 5. Freezing and Melting Points of Sulphuric Acid . 132 6. Boiling Points of Sulphuric Acid . 132 7. Fusing Points of Nordhausen Oil of Vitriol . 133 8. Percentage of SO3 in Nordhausen Oil of Vitriol . 134 9. The Quantitative Estimation of Free Sulphuric Acid . 136 10. Examination of Sulphuric Acid for other Substances 136 (a) Nitrous Acid (Nitrososulphuric Acid) 135 Table for expressing the Results . . . 186 (&) Total Nitrogen Acids ; Nitrometer . . 137 Gas-volu meter ...... 139 (c) Relative Proportions of the Three Nitrogen Acida . 142 (d) Qualitative Test for Traces of Nitrogen Acids . 142 (e) Selenium ; (/) Lead ; (g) Iron . . . 143 (Tb) Arsenic ; (i) Chlorides ...... 144 11. Analysis of Fuming Sulphuric Acid (Nordhausen Oil of Vitriol) and of Sulphuric Anhydride .... 144 III. Saltcakb and Hvdrochloric Acid :— A. Salt (Common and Rock Salt) . . 146 1. Moisture; 2. Insoluble; 3. Chlorine . . 146 4. Lime; 5. Sulphates; 6. Magnesium Chloride . 147 B. Saltcake (Sulpliate of Soda). — 1. Free Acid 2. Sodium Chloride ; 3. Iron; 4. Residue; 7. Alumina ; 8. Sodium Sulphate C. Chim/ney-Testing. — Act of Parliament Hydrochloric Acid in Chimney Gases . D. Testing of the Gases in the Hargreaves' Process E. Hydrochloric Add. — Specific Gravities at 15° 2. Influence of Temperature on the Speciflc Gravity . 3. Analysis of Hydrochloric Acid : (a) Estimation of HCl (6) Of Sulphuric Acid ; (c) Iron ; (d) Free Chlorine (e) Sulphur Dioxide ; (/) Arsenic . Lime; 6. Magnesia 147 148 148 149 149 151 152 153 153 154 154 xii CONTENTS IV. Bleaching Powder and Chlorate of Potash Manufacture : — page A. Natural Manganese Ore. — 1. Manganese Dioxide . 155 2. Carbon Dioxide .... 155 3. Hydrochloric Acid required for Decomposing the Ore 156 B. Recovered Manganese Mud and Wddon Liquors . 156 1. MnOg in Weldon Mnd ; 2. Total Manganese of the Mud . 156 3. Estimation of the Base (the Monoxides) 157 C. Limestone. — 1. Insoluble; 2. Lime . 157 3. Magnesia; 4. Iron . . . 15S D. Quicklvme.—l. FreeCaO; 2. Carbon Dioxide . 158 E. Slaked Lime.— 1. Water; 2. Carbon Dioxide ; 3. Specific Gravities 158 Amount of Lime in Milk of Lime . . 159 F. Bleaching Powder. — 1. Available Chlorine . . . 159 2. Comparison of the Percentages with the French (Gay-Lussac) Degrees . . 160 3. Carbon Dioxide, Lnnge and Rittener's Process 160 4. Testing the Atmosphere of the Chambers before opening them . 161 G. Deacon Process.— 1. Proportion of HCl and CI in the Gases . 162 2. Carbon Dioxide . . . 162 3. Steam . . . 163 H. Electrolytic Chlorine.— 'Exa.mmaXion foT CO2 163 I. Chlorate of Potash .... 1G4 1. Chlorate Liquors : (a) Chlorate; (&) Chloride 164 2. Commercial Chlorate of Potash . 164 K. Bleach Liquors . . . 164 L. Liquid Chlorine. — Pressure and Specific Gravities . 165 V, Soda Ash Manufacture by the Leblanc Process : — A. Raw Materials . ... . . 166 1. Saltcake; 2. Limestone or Chalk ; 3. Mixing Coal . 166 B- Black-Ash ... .166 1 . Tests made with the Muddy Mixture :— (a) Free Lime . . . 166 (6) Total Lime ... .167 2. Tests made with the Clear Portion : — (a) Available Alkali and Sodium Carbonate 167 (&) Caustic Soda . 167 (c) Sulphide ; (d) Chloride . . .168 (e) Salphate ; (/) Carbonated Sample 168 C. Tank Waste (Vat Waste).— 1. Available Soda . . 168 2. Total Soda ; 3. Total and Oxidisable Sulphur 169 D. Tank Liquor (Vat Liquor). — 1. Sodium Carbonate 169 2. Hydrate; 3. Sulphide . . 169 4. Sulphate ; 5. Total Sulphur . 170 6. Chloride; 7. Ferrofiyanide . 170 5. Silica, Alumina, and Ferric Oxide . . 170 9. Carbonated Sample . . . 171 E. Carbonated Liquor. — Test for Bicarbonate . . 171 Lunge and Bittener's Process for estimating COg . 171 F. Motlier Liquor.— (a) Sulphate ; (6) Other Compounds of Sulphur 173 CONTENTS xiii V. Soda Ash Manufacture by the Leblanc Pbocbss— Corotinwed;— page G. Tables of Specific Gravities : — 1. Specific Gravities of Solutions of Sodium Carbonate at 15° C. 174 2. Specific Gravities of Concentrated Solutions of Sodium Carbonate at SO" C. . . . . . . . .175 8. Infiuence of Temperature on the Specific Gravities of Solutions of Sodium Carbonate . . . . 176 H. Analysis of Commercial Soda Ash . . . . . . 178 Table for comparing French, German, and English Commercial Alkalimetrlcal Degrees . . .180 I. Sulphv/r Recovery (Chance Process) ...... 182 1. Sulphur as Sulphide in Vat "Waste . . 182 2. Sulphur as Sulphide in Carbonated Mud . . . 182 3. Sulphide-Sulphur+COa in Vat Waste . 182 4. Sulphur in Solutions ... . 183 5. Soda, Lime, and Thiosulphate in Liquors . 188 6. Lime-kiln Gases . . . 183 7. Gas from Gas-holder . . ... 184 8. Exit Gases from Claus Kilns . . .184 VI. Manufacture of Soda by the Ammonia Process :— A. Raw Materials.— I. Rock Salt; 2. Brine. . . . 186 3. Gas Liquor or Sulphate of Ammonia .... 185 4. Limestone ; 5. Quicklime ; 6. Coals or Coke . . 185 B. Tests made during the Ma/nufacturing Process : — 1. Ammoniacal Brine : (a) Chloride ..... 185 (6) Ammonia, Free and Combined ..... 186 2. Carbonators; 3. Mother Liquor ; 4. Crude Bicarbonate 186 5. Distillation of Ammonia; 6. Llme-kiln Gases . . . 186 C. Commercial Products. — 1. Soda Ash; 2. Commercial Bicarbonate . 186 VII. Caustic Soda: — A. Caiistic Liquor.— (a) Available Alkali ..... 186 (6) Table of Specific Gravities of Sodium Hydroxide at 15' C. 187 (c) Infiuence of Temperature on the Specific Gravities of Caustic Soda ....... .190 B. Lime Mud.— (a) Sodium as Carbonated Hydrate . . . 192 (&) Caustic Lime ; (c) Calcium Carbonate .... 192 C. Fished Salts; D. Caustic Bottoms ...... 192 B. Commercial Caustic Soda ....... 193 VIII. Electrolytic Alkaline Liquors: — 1. Hypochlorites ; 2. Free Hypochlorous Acid ; 3. Chlorate 193 4. Chloride; 5. Carbon Dioxide ; 6. Bases; 7. Free Alkali 194 IX. Nitric Acid Manufacture : — A. Commercial Nitrate of Soda : — General Remarks ; Refraction ; Sampling 1. Moisture ; 2. Insoluble ; 3. Sodium Nitrate 4. Sulphate; 5. Chloride; 6. Iodine . 7. Potassium ; 8. Perchlorate . B. Nitre-Cake.— 1. Free Acid; 2. Nitric Acid 8. Ferric Oxide and Alumina . 195 195 196 197 197 197 xiv CONTENTS IX. Nitric Acid Manufacture— CoTiMTiifred ; — face C. Nitric Add.—!. Specific Gravity of Nitric Acid at 15' C. . . 198 2. Inflaence of Temperature on the Specific Gravity of Nitric Acid 201 3. Total Acidity ; 4. Oblorine ; 5. Salphnxic Acid . . 203 6. Nitrons Acid or Nitrogen Tetrozide ; 7. Fixed Besidne . 203 S. Iron; 9. Iodine ... . . 203 D. Mixtures of Sulphuric Acid and Nitric Acid. — 1. Total Acidity 204 2. Nitrous Acid; 3. Nitrogen Acids ; 4. Sulphuric Acid . 204 X. Potassium Salts : — A. Crude Salts (Camallite, Kainite, etc.) 1. Moisture .... 2. Percentage of Potassium : — (a) In the Absence of more than 0-5% Potassium Sulphate (b) In the Presence of more than 0-5% Potassium Sulphate S. Percentage of Sodium Chloride ; 4. Magnesium Chloride 5. Total Magnesium B. Commercial Potassium Chloride C. Potassium Sulphate . . .... D. Leblanc Process for the Manufacture of Potassium Carbonate B. Beet Ashes . ... F. Commercial Carbonate of Potash . , . . G. Tables:— 1. Specific Gravities of Solntions of Potassium Carbonate at 15" 2. Influence of Temperature on the Specific Gravities 3. Specific Gravity of Solutions of Potassium Hydroxide . 205 205 205 205 206 207 207 207 207 207 207 212 214 XI. Ammonia Manufacture :— A. Gas-Liquor. — 1. Volatile Ammonia; 2. Total Ammonia; 3. Total Sulphur .... 4. Thiocyanate ... . . B. Sulphate of Ammonia. — Estimation of Ammonia . C. Liquor Anvmonics 1. Specific Gravities of Solutions of Ammonia 2. Specific Gravities of Solutions of Ammonium Carbonate 217 218 219 220 221 222 XII. Manufacture of Coal-Gas (Illuminating Gas): — A. Coal-Gas. — Apparatus; Notes on the Bunte Burette Taking Samples ; Measuring the Gas in the Burette Introduction of the Absorbing Liquids 1. Carbon Dioxide ; 2. Heavy Hydrocarbons 3. Oxygen ; 4. Carbon Monoxide 5. Hydrogen .... 6. Methane ; 7. Nitrogen B, Purifying Material (^Spent Oxide). — 1. Cyanogen; 2. Sulphur 222 223 224 224 224 225 226 227 XIII. Calcium Carbide and Acetylene : — A. Raw Materials ; B. Technical Calcium Carbide 228 XIV. Examination of the Raw Materials and Products of the Manu- facture OF Fertilisers : — A. Sampling; B. Moisture . . CONTENTS XV XtV. BXAMIHATION Of THE RAW MaTSEIALS, BTO.— CoTlfWIWtf ;— I'AGE C. The Insoluble Matter : D. Phosphoric Acid . . . 230 1. Preparation of the Solutions . ... .230 (a) Phosphates Soluble in Water . . . 230 (b) Phosphates Soluble in Ammonium Citrate . 230 (c) Total Phosphoric Acid .... 230 (<2) Thomaa-Slag Phosphates ... 230 2. Examination of the Solutions : For Phosphoric Acid S31 (n) Molybdenum Method ; (!i) Citrate Method . . 231 E. Free Acid; P. Ferric Oxide and Alumina . . 232 G. Nitrogen. — 1. Nitric Nitrogen ; 2. Ammoniacal Nitrogen 233 3. Total Nitrogen 233 4. Organic Nitrogen 233 H. Potash . ■ 234 XV. Alumina Preparations;— A. Raw Materials. — 1. Kaolin (China Clay) ; 2. Bauxite . 234 B. Control of Working Conditions . . . ; 236 C. Commercial Prodv/Cts. — 1. Sulx^hate of Alumina and Alum 236 (a) Estimation of Alumina . . . 235 (b) Iron, Lunge and Eeler's Method . ^36 (c) Free Acid ; (d) Zinc .... .237 2. Aluminate of Soda : (a) Soda and Alumina . 237 (b) Insoluble ; (c) Silica . . 237 3. Commercial Alumina ..... 237 XVI. Cement iHunsTRy:— A. Portland Cement.— 1. Raw Materials, (a) Limestone; (i)) Clay . 238 Complete Analysis ; — 1. Decomposing by means of Allcaline Carbonate . 238 2. Alkalies ; S. Sulphur 239 4. Carbon Dioxide ; 6. Loss of Weight on Ignition . . 239 (c) Separation of Silica present as Quartz, and such present in the form of Silicates ... . . 239 Process of Lunge and Milberg .... 239 2. Control of Working Conditions . . . 240 3. Commercial Cement.— (.a) Silica; (6) Alumina+Ferric Oxide . 240 (c) Ferric Oxide ...... 240 (d) Lime ; (e) Magnesia ; (/) Sulphates . . .240 (j) Total Sulphur; (A) Allialies; (i) Physical Tests . . 241 B. Bydraulic Lime and Roman Cement ... . 241 0. Puzzuolanas, Trass, .Granulated Blast-Furnace Slag . . 241 XVII. Preparation of Standabd Solutions: Introductory .... A. Normal Acid and Alliali Indicators Standard Alkali Corrections for Temperature B. Potassium Permanganate . C. Iodine Solution ; Starch Solution D. Sodium Arsenite Solution ; B. Silver Solution F. Copper Solution ; G. Oxalic Acid Solution 241 242 243 245 246 246 247 xvi CONTENTS PAGE XVIir, Rules for Sampling: — . . 249 A. Fuel ... ■ . . . 249 B. Ores and Minerals {Pyrites, ManganesBj Salt, etc.) . . 249 (a) Smalls, Slack, Salt, or otber Substances not requiring to be Crushed .... . 249 (b) Ores in Pieces requiring to be Crushed . . 250 C. CAemicaZs.— Saltcake, Soda Ash ; Bleaching Powder ■ ■ 261 Caustic Soda ; Solid Sulphuric Anhydride . . - 252 XIX. Comparison of the Hydrometer Degrees according to Baum£ AND TWADDELL, WITH THE SPECIFIC GRAVITIES . • . 253 XX. Value op Alkali per Ton 255 Index . 269 GENERAL TABLES NOTE Ali. temperatures are given in degrees Centigrade, unless otherwise stated. The atomic weights are those adopted by the International Committee on Atomic Weights for the year 1916, as given in Table No. 1 referred to. Oxygen = 16. INTERNATIONAL ATOMIC WEIGHTS a?ABLB 1.— INTERNATIONAL ATOMIC WEIGHTS According to the Table issued by the International Committee on Atomic Weights for 1916. Aluminium . Al 27-1 Neodymium Nd 144-3 Antimony . Sb 120-2 Neon . Ne 20-2 Argon . Ar 39-88 Nickel Ni 68-68 Arsenic As 74-96 Niobium Nb 93-6 Barium Ba 137-37 Niton . Nt 222-4 Beryllium . Be 9-1 Nitrogen N 14-01 Bismuth Bi 208-0 Osmium Os 190-9 Boron . B 11-0 Oxygen O 16-00 Bromine Br 79-92 Palladium . Pd 106-7 Cadmium Cd 112-40 Phosphorus . P 31-04 Caesium Cs 132-81 Platinum . Pt 196-2 Calcium Ca 40-07 Potassium . K 39-10 Carbon C 12-005 Praseodymium Pr 140-9 Cerium Ce 140-25 Radium Ra 226-0 Chlorine CI 35-46 Rhodium . Rh 102-9 Chromium . Cr 52-0 Rubidium . Rb 85-45 Cobalt. Co 58-97 Ruthenium . Ru 101-7 Copper Cu 63-37 Samarium ' . Sm 150-4 Dysprosium Dy 162-5 Scandium . Sc 44-1 Erbium Er 167-7 Selenium Se 79-2 Europium . Eu 152-0 Silicium Si 28-3 Fluorine F 19-0 Silver . Ag 107-88 Gadolinium Gd 157-3 Sodium nI 23-00 Gallium Ga 69-9 Strontium . Sr 87-63 Germanium Ge 72-5 Sulphur S 32-06 Gold . Au 197-2 Tantalum . Ta 181-5 Helium He 4-0 Tellurium . Te 127-5 Holmium Ho 163-5 Terbium Tb 159-2 Hydrogen . H 1-008 ThaUium . Tl 204-0 Indium In 114-8 Thorium . Th 232-4 Iodine I 126-92 Thulium . Tu 168-5 Iridium Ir 193-1 Tin . Sn 118-7 Iron . Fe 65-84 Titanium Ti 48-1 Krypton Kr 82-92 Tungsten . W 184-0 Lanthanum La 139.-0 Uranium . u 238-2 Lead . Pb 207-20 Vanadium . V 51-0 Lithium Li 6-94 Xenon X 130-2 Lutetium . Lu 175-00 Ytterbium . Yb 173-5 Magnesium Mg 24-32 Yttrium Y 88-7 Manganese . Mn 54-93 Zinc . Zn 65-37 Mercury Hg 200-6 Zirconium . 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OS »»^ (U (U O "^ (N TO W W "^ 5/j ^ ooooo -o a a a a -*QCD a a be 5 'SI'-' ■3.SII H|0 C*5OlQ0 CO-^JT'-OOCOOSOOOVOCO-^fNCD OA'»«D00>X5tHCD <£> i-H J>- CM 00 «5 t^ O CO ^14 1C3 OS O OO (M -^ r>. iCJ OO (N £N \C3 CO rHf-l(N (MCOCNtNCOlN (M C^(M i-H (Ni-trH(N X q> 4J . (litharg lead) . de '. droxide oride . s nate hosp ite, c ide. oxide e O P-Jj °-^^ onoxide ide (red rbonate Loride phate Iphide ium oxi ^h^ O OlM Pi toT3 1 -M a§g-ggg| 1 ^ i u I— I s s s i ^ bp g. 8 THE TECHNICAL CHEMISTS' HANDBOOK -K lO CO lO HH to o y t^ O rH „ Soqq.'PS 3; « Oi .^ 10 ,- CO OS • g^ 2 ""I CO " 00 0000^0 -^ CD 10 CO CO OD Oi t-H O O Tfl -•'■^ oooooSo C4 91 IM Ct Ci] C4 S$0 (NOOOOOO-*COQOO-^«Til-^ ■^Olt^QOi-HOSloeOOOSlNt^Oa 1-1 i-l -^ r-l r-\ N 1-t t-H cS Hi m • . o is -J' . . ^ . . . . ^ ^ 9. „a S K •. „do>§ Md8°d 9' !• 3 -a • • sg. • 'a b " -^ — ttj " .a "2 B 'S o . J3 0-32 2 io3o ° 'is 9 3-E S |3 c8 m a S « us o<.-„ •a 'o c o 'x " <* O to m is is is ;3 .j5 . . . . ^2-S &.§ . . x o - o "O o . ■§o2 « OJ CJ ■ o Pi td 5 1 -2 s~ s e 2 M SYMBOLS, MOLECULAR WEIGHTS, ETC. Of mooo S"o"ot 5 --73 '"oi o »o ■•• (O »C CO . 'ooo el oi oj W M »4 HH i-f 1-1 "^ CO OS •* 00 o6. Oo oo§o HH M Ph M 3 .sj ■§ . (U d ■S S (D « ** d -3 -^ « => fe- us £1 «^ . a " « « « « u uT 32 22 n K r! S CO SYMBOLS, MOLECULAR WEIGHTS, ETC. 11 a o O a 1-1 < o.S'll Pi 0>a to 9^ tncc OO ivi VI m oiojOCC « OO •-? - o 'A 00 , o CO lO lO ^ ^_, O O m«J « mccMScc O OS mooS ,V, _. °° •'to JT'J' PlM ■ O 1* lo j:^ oc o rij OS l>- • S -^ (N O Q .. ..CO OS O 00 '-t n ^ a ^ '^ CO i-H rH (N ■^(OOOi-HCDi-Ht-t- coc^iHcocoeooooi .q OM ?oo o Q. o + •o c/3 en K li! cooOOOmmw k u2 w n is) si n si rS CO 3 o CO .^ a a o CO Ji 3 .a a Of eg CO ■3 C3 J3 CO ;§ 2 ^ ^ u u 'Sob. Oi ><.a a 3 CO •5^ art CO 12 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 3.— FACTORS FOR CALCULATING GRAVIMETRIC ANALYSES. Substance weighed. Substance to be determined. 1. log Ammonium. Ammonium chloride, NH4CI 1 Ammonia, NH3 Ammonium oxide. 0-3183 0-50286 -1 Ammonium platinum J chloride, (NH4)2PtCl6 . i {iill,\0 . . 0-1174 0-06967 -1 Ammonia, NH3 0-0767 0-88486 -2 \ Nitrogen N 0-0631 0-800009-2 Arsenic. Arsenic, As . 0-6091 .0-78470 -1 Arsenic trioxide. Arsenic trisulphide, AS2S3 . • AS2O3 . Arsenic anhydride. 0-8041 0-90533 -1 ASaOg . 0-9342 0-97042 -1 Arsenic, As 0-3939 0-59532 -1 Ammonium magnesium Arsenic trioxide, arsenate, MgCNHjjAsOi - AS2O3 . . . 0-5200 0-71595 -1 + 4aq Arsenic anhydride. AsA . 0-6040 0-78104 -1 Barium. Barium sulphate, BaSOi . l fBaO 0-6570 0-81756 -1 Barium carbonate, BaCOj . [ Barium oxide,-! BaO 0-7771 0-89046 -1 Bariumsilicofluoride,BaSiFeJ (.BaO 0-5483 0-73905 -1 Calcium. Calcium sulphate, CaSO^ . \ ' Calcium carbonate, CaCOg / Calcium oxide, 1^^ 0-4119 0-5603 0-61484 -1 0-74843 -1 Carbon. ^ Barium carbonate, BaCO^ . Carbon dioxide, COg 0-2229 0-34817 -1 Calcium carbonate, CaCOs . Carbon dioxide, COg 0-4397 0-64314 -1 Carbon dioxide, COj . Carbon, C 0-2727 0-43573 -1 Chlorine. ' Chlorine, CI . Chloric anhydride. 0-2474 0-39337 -1 CA • • • 0-5264 0-72135 -1 Potasium chlorides. Silver chloride, AgCl . ] KCI . Sodium chloride. 0-5202 0-71614 -1 NaCl . 0-4078 0-61049 -1 Hydrogen chloride. I HCl . 0-2544 0-40557 -1 Copper. Cupric oxide, CuO . Copper, Cu 0-7989 0-90250 -1 Cuprous sulphide, CugS . < Copper, Cu Cupric oxide, CuO . 0-7986 0-9996 0-90231 -1 0-99981 -1 Hydrogen. Water, H^O Hydrogen, H . 0-1119 0-04884 -1 Iron. , Ferric oxide, Fe^Os . . | Iron, Fe . . . 0-6994 Ferrous oxide, FeO 0-8998 0-84470 -1 0-95416 -1 FACTORS FOR GRAVIMETRIC ANALYSES 13 TABLE 3—Contmtied. Substance Weighed. Substance to be determined. 1. log Iiead. Lead monoxide, PbO . Lead, Pb 0-9283 0-96768-1 Lead sulphate, PbSOi . | Lead, Pb Lead oxide, PbO . 0-6831 0-7359 0-83449-1 0-86681-1 Lead sulphide, PbS . | Lead Pb . Lead oxide, PbO . 0-8659 0-9328 0-93747-1 0-96979-1 Lead, Pb .... Lead oxide, PbO . 1-0773 0-03234 Magnesium. Magnesium pyrophosphate, Magnesium oxide. Mg^PA .... 0-3621 0-56883-1 Magnesium sulphate, MgSOi Magnesium oxide, MgO . . . 0-3349 0-52493-1 Manganese, Mangano manganic oxide, Ma^Oi .... Manganese, Mn 0-7203 0-85749-1 r Manganese, Mn 0-6314 0-80029 1 Manganese sulphide, MnS -1 Manganous oxide. I MnO . 0-8153 0-91131-1 'Nitrogen. Ammonium platinumchloride, (NH4)2PtCle . . . Nitrogen, N . 0-0631 0-80009-2 Platinum, Pt . Nitrogen, N . 0-1435 0-15699-1 Phosphorus. Magnesium pyrophosphate, MgaP^O, .... j" Phosphorus, P -i Phosphorus pent- 0-2787 0-44519-1 (. oxide, PgOj 0-6379 0-80477-1 Potassium. Potassium chloride, KCl Potassium oxide. K^O . . . 0-6317 0-80051-1 Potassium-platinum chloride, C Potassium oxide 0-1930 0-28556-1 KgPtCIg (reduction factors-] Potassium chloride 0-3056 0-48515-1 adopted at Stassfurt) . [ Potassium sulphate 0-3571 0-56279-1 Potassium sulphate Potassium oxide . 0-5405 0-73282-1 Sodium. Sodium sulphate, NajSO^ . Sodium carbonate, NaaCO, . Sodium oxide, NagO 0-4364 0-63989-1 Sodium oxide, NagO 0-5849 0-76708-1 Sodium chloride, NaCl . Sodium oxide, Na^O 0-5303 0-72460-1 Sulphur. /* Sulphur, S 0-1374 0-13792-1 SulphurdioxidcSOa 0-2745 0-43847-1 Sulphur trioxidcSOa 0-3430 0-63629-1 Barium sulphate, BaSO^ Sulphuric acid, riaS04. . , 0-4202 0-62344-1 Sodium sulphate, _ Na^SO^ . . 0-6086 0-78432-1 Zinc. Zinc oxide, ZnO . Zinc, Zn . 0-8034 O'90492-l Zinc sulphide, ZnS Zinc, Zn . Zinc oxide, ZnO 0-6709 0-8351 0-82664-1 0-92172-1 14 THE TECHNICAL CHEMISTS' HANDBOOK ® a CO fa 01 m o ■a *i o X "^ |ii s CO .4 3 •» O D % s ^ b ^1 M 1 « g W n a fi i o S (D It n 1 :§ .S 1 ^ ^ >* * o -i B 1-^ 3 u o Leduc. Saussure. (at 22r) Jahn. Treadwell. Rayleigh, Leduc. Guye. Saussure. Morley. Scheuer. Baume, Perrot. Rayleigh, Leduc. Guye. Guye. Guye. Baume, Perrot. Ja'querod, Pintza. 1 o CO OO C9 !>. ^ - O CO OO »0 CD ■«il rH t^ OS lO OS CO 'V £^ OS CD »« O CO o<» .(NoseotNoocDcDvacDcflco : :o loseo : ; Oi .rs * WS Ttl OS W3 OS O « i£3 OS lO O - ■ r-t • ^H M • " OO \0 (N O 1^ O O iH O O 1^ Ai Ah 1-1 -Oi-tt*.-HtDC^ oo»po»nTj(osipoioc^wsoiw30u:si-irHcq.--«CT^^ OO.-Hi0(NOi^OoAhOOi^Aii^W.^CTi^(NW0 2 1.3 1 1 o OO asi-HCOoot^co-^oi/s^^ci (M cM(d oso i-iosocDcooiasecioi>-o os oseo oot- :-*r-(ioj>-x>-oocoi-tirtt^-TP : ;(M :co(m : : 7^^ ' r* '?' 'T' ?* *?* 9* "P ^ *?* *? 7^ • * "? • "P 9* * * i-Hi-f l>.COrHi~lrHOi-lOi-l»-H>-) ,-1 i-HCq 1 'a 1 OCOOOQO-^Wii-tCSOOSOl'^OOOOSCOCQOCOiOCTO I— 10IMOOt*0»r3T-(000»Oi-(CDOTPOSOS.-i(M,-l o u> S > Of CO a H S§ -g O pq gg M 1^ 73 fn a -J3 bo ,• tH a R o S "O as ,J3 " a f b A O C5 H c ■" 15 H ■2=8 <1 hi] D «5 CQ iri -i-t-'*-(NCOO(Ni>-C3i(M.-iOTtlo:j-<* COJ>-OOt>-^-vO'^J>.Ot-COOOOt>-COI>- «i OOCOC<1«DOOOOOO(M'»OOCOOOOOCD(M ooim^-iouacooooscOr-tThiot-M^ura 5000i>.000SOO(MaS'*iO'^0000»^i-IC0 oocnioc>ic^C)u:5i^«5eo^pt^ooi>-cocN i^ioD4)coost*oaj?^oiMa>0'ij(NCT>os oooooioioooooiooicavoioo T:t<-*CDCO(MI^IMOCni-IOOr-(»-*.-H.-(Vfi«> OOOO'^t^r-.COiOOOOlCSlOOOt^OOOiOS os(Ml>-coas»o«D£--cot-coeooo-#ooe£M>- Ol .-H t-H i-H i-H r-l ■* (MC^00-*OOOO-OQO(NC005DC»iOOO.t^iO CJsos^cp»rsepOpf^c^ipcoi>-(rfli^oOi^ i-H i-H rH i-l i-H ,-H en ■^-^cor-wsioi^ao-^coosOitNOJoacoeo OOl>.COt^lNT-lOiOTl-t^cNoi"pi>*»pcp5OOTpp-ctic0«0(M-* MCOCOOiiOVni-HOCOCOi-HO-^OOCNOOQO lOOSiOIMCDCOO-^COi-tiaoOOSiMOlCOt^ ca-oQu:5ou^wwcpco'X'iri-^p ^ rH rH 1 1 l:^OOiCD!M(NOS'*-osoiosi>-£^ cnKiiOlOCOOOSOOOOlOStNIM-^i^OQO CqprHO0»pU^prHr-I.^I>-r-((NTt<»r3»ft,-H ooooooooooooooooo - OOOOfMiaSOOvOOCOlMCOCOTjICOCOrHtN 5c>coas"^-oorHoow^ot^Tjicoascs t^CSMi-HOOCOmiNOOlCStN-^Oii-HOlrHCO p-?if'^t*ooiH(rq»ftcqipi:c)oocDcoi,--csin T-H-^i-HOCOCOrHi-HiHrHOrHi-tNCOCOrH i b II II II II II II II II II II II II II II II II II 16 THE TECHNICAL CHEMISTS' HANDBOOK 1 o >o . . ■ a wj : t^ :os : w la :^ ooipoa : I-KM5DCT too' la i^ a O ia to N asOCOwA^rHCO OS O iH CO o *^t^o»n»ONO ^■ 1 .2 -a 1 o I o s Potassium hydrate chromate (neutral) bichromate oxalate (acid) . . permanganate . thiosulphate bitartrate . tartrate (neutral) cyanide ferrocyanide ferricyanide iodide . Sodium acetate . borate . bromide . . . iodide . . . hydrate . thiosulphate . phosphate (ordinary) sulphite . Strontium hydrate nitrate chloride Tartaric acid Tin (stannous) chloride o • >o 2 :o ; 1^ 00 (NO :o 00 \at^^ CO :o : Oa-^OiOcHOO-^rHO OOOSOOUSCOf-iMt- ' ?00 O lO 00 i# t* 50 -* « C^ CO i-l »0 t- CO -^ t^ C^ tH O j-f 1-^ 00 i-l CO (N lO r^ i-H i-H So CO CO i-H C» Ttt O O (N O O r-l »p ip lAOOiH «50rH CO -0> OOO lOin CO 4f< CO Tti Cq 00 (N TO OO Ot* O OSt^ -* CD O 00 ' ' ' ot^ CO «0 CO r-l OrHOOlN-* ■<* fr.. i-H i-t i-H 1 1 1 ■3 t o O Alum, ammonium potassium Aluminium sulphate Ammonium oxalate nitrate Barium chloride . hydroxide nitrate . Boric acid . Bromine Calcium carbonate hydroxide nitrate . Copper acetate . nitrate . sulphate . Ferric chloride . Ferrous sulphate Lead acetate chloride nitrate sulphate Magnesium oxide carbonate Manganous chloride Oxalic acid . SOLUBILITY OF SALTS 17 to 1 1 J3 i o Poggiale. Dibbits. Mulder. Mulder. Roozeboom. Hulett and Allen. Van't Hoff, Meyerhoffer. Loewel, Mulder, Meyerhoffer. Gay-Lussac. Andrese, Mulder. > Pickering. Andreae, Berkeley. Andrese, Berkeley, Trevor. Dibbits. Mulder, Loewel, Epple. Kremers, Graebe. Andrese, Berkeley. Pickering. Berkeley. Loewel, Gay-Lussac. Horn and van Wegener. Taylor. Mylius and Dietz. Cobeii, Callendar & Barnes, Etard. t n °i rH « « rH ip ® ^ ^ T* ^ K' ^ *P OS ; ^- OT OS o CO 00 «o i> 00 e« 4(1 • in •* OS o »ri (?q cq eo m 00 40 t* o lo t^ eo lO lo ** -* (N TJH o CO ■* t^ -511 »o C© rH t^ w (-1 i-l (N CN CO t-l W «0 1 a e So 1 1 1 "S 1— 1 ' J3 o t^ )H . -^ "H ^ Ot*i-IOO(NO«OOOt^«D»n«A)OrH«>OseoOK»' «■ a. «• •04890 •006948 •02148 ■0001922 •02388 •002 977 1 •04759 •006758 •02126 •0001902 •02337 •002912 2 •04633 •006576 •02105 ■0001882 •02288 •002843 3 •04512 •006401 •02084 •0001862 •02241 •002790 4 •04397 •006234 •02064 •0001843 •02196 •002732 S •04286 ■006074 •02044 •0001824 ■02163 •002677 6 •04181 •005920 •02025 •0001806 ■02111 •002624 7 ■04080 •005775 •02007 •0001789 ■02070 •002670 8 •03983 •005633 •01989 •0001772 ■02031 •002620 9 •03891 •005499 •01972 •0001756 ■01993 •002472 10 ■03802 •005370 •01955 •0001739 ■01956 •002424 3 •695 •9969 11 •03718 •005248 •01940 •0001725 ■01920 •002378 2^996 •9652 12 ■03637 •005129 •01925 •0001710 ■01885 •002333 2-900 ■9344 13 ■03560 •005011 •01911 •0001696 ■01851 •002289 2 ■808 ■9048 14 ■03486 •004908 •01897 •0001682 ■01818 •002246 2^720 ■8766 15 ■03415 ■004804 •01883 •0001669 ■01786 •002205 2 ■635 ■8493 16 ■03347 ■004703 •01869 •0001654 ■01755 •002164 2 ■553 ■8230 17 ■03283 ■004609 ■01856 •0001641 ■01725 •002125 2^474 ■7977 18 ■03220 •004515 ■01844 ■0001630 •01698 •002089 2^399 ■7736 19 ■03161 •004428 ■01831 ■0001616 •01667 ■002049 2 ■328 ■7608 20 ■03102 •004339 ■01819 ■0001604 •01639 ■002012 2 ■260 •7291 21 ■03044 •004253 ■01805 ■0001590 •01611 ■001975 2^200 •7098 22 ■02988 -004169 ■01792 ■0001575 •01584 ■001940 2^143 •6916 23 ■02934 •004088 •01779 ■0001561 •01557 ■001903 2^087 •6737 24 ■02881 •004009 •01766 •0001548 •01530 •001868 2 ■OSS •6570 25 •02831 •003932 •01764 •0001534 •01504 •001832 1^985 •6411 26 •02783 ■003859 •01742 •0001622 •01478 •001798 1^937 •6267 27 •02736 ■003787 ■01731 •0001609 •01453 •001764 1^891 •6110 28 •02691 ■003717 ■01720 •0001497 •01428 •001731 1^848 •5973 29 •02649 ■003653 ■01709 ■0001485 •01404 ■001699 1-808 ■5846 30 •02608 ■003588 ■01699 ■0001470 •01380 ■001666 1^769 ■5722 35 •02440 •003315 ■01666 ■0001426 •01271 ■001516 1^575 •5103 40 •02306 ■003081 ■01644 •0001386 •01182 ■001386 1-414 •4589 45 ■02187 ■002860 •01624 •0001338 •01111 ■001275 1-300 •4227 50 •02090 ■002657 •01608 ■0001288 •01061 •001184 1-204 •3927 60 •01946 •002274 •01600 ■0001178 •01000 ■001026 1-006 •3294 70 •01833 •001857 •01600 ■0001021 ... ... 0-848 -2792 80 •01761 •001381 •01600 ■0000790 .>• • >. 0-672 ■2226 90 •01723 •000787 •01600 ■0000461 0-380 •1268 100 •01700 ■000000 •01600 ■0000000 •01000 ■000000 0-000 ■0000 SOLUBILITY OF GASES IN WATER TABLE S—Contmued. 19 Carbon monoxide, Carbon dioxide, Hydrogen sul- Ammonia, T. W. B. &B. pliide, P. B .. 3- a. 2- .. a. u.. 8- 0-03537 0-004397 1-713 0-3347 4-686 0-710 1298-9 98-7 1 0-03455 0-004293 1-646 0-3214 4- 555 0-689 1220-2 92-7 2 0-03375 0-004192 1-584 0-3091 4- i28 0-670 1154-7 87-7 3 0-03297 0-004092' 1-627 0-2979 4- 303 0-651 1100-9 83-6 i 0-03222 0-003997 1-473 0-2872 4- 182 0-632 1053-0 79-9 5 0-03149 0-003904 1-424 0-2774 4- 363 0-615 1019-5 77-3 6 0-03078 0-003814 1-377 0-2681 .3- 348 0-596 997-2 75-6 7 0-03009 0-003726 1-331 0-2590 3- 336 0-579 974-9 73-9 8 0-02942 0-003641 1-282 0-2494 3- r28 0-562 954-5 72-3 9 0-02878 0-003560 1-237 0-2404 3- 322 0-546 933-0 70-6 10 0-02816 0-003481 1-194 0-2319 3- 520 0-530 910-4 68-9 11 0-02757 0-003416 1-154 0-2240 3- 121 0-515 888-0 67-2 12 0-02701 0-003333 1-117 0-2166 3- 325 0-500 865-6 65-5 13 0-02646 0-003260 1-083 0-2099 3- 332 0-485 843-2 63-7 14 0-02593 0-003188 1-050 0-2033 3- 142 0-471 822-1 62-1 15 0-02543 0-003130 1-019 0-1971 3- 356 0-458 802-4 60-6 16 0-02494 0-003065 0-985 0-1904 2- 373 0-445 783-2 59-1 17 0-02448 -003007 0-956 0-1845 2- 393 0-433 764-1 57-6 18 0-02402 0-002943 0-928 0-1789 2- 316 0-421 744-3 56-1 19 0-02360 0-002893 0-902 0-1736 2- r42 0-409 725-8 54-7 20 0-02319 0-002839 0-878 0-1689 2- 372 0-398 710-6 53-6 21 0-02281 0-002789 0-854 0-1641 690-2 51-9 22 0-02244 0-002739 0-829 0-1591 674-3 50-6 23 0-02208 0-002691 0-804 0-1541 661-0 49-6 21 0-02174 0-002647 0-781 0-1494 647-8 48-6 25 0-02142 0-002603 0-769 0-1450 634-6 47-6 26 0-02110 0-002560 0-738 0-1407 621-3 46-5 27 0-02080 0-002519 0-718 0-1367 • 608-1 45-5 28 0-02051 0-002479 0-699 0-1328 594-8 44-4 29 0-02024 0-002442 ; 0-682 0-1293 . ... 30 0-01998 0-002405 0-665 0-1259 35 0-01877 0-002231 0-592 0-1106 40 0-01775 0-002076 0-630 0-0974 45 0-01690 0-001934 0-479 0-0862 50 0-01615 0-001797 0-436 0-0762 ■• ! 60 0-01488 0-001521 0-359 0-0577 70 0-01440 0-001276 80 0-01430 0-000981 90 0-01420 0-000568 100 0-01410 0-000000 ... ... 20 THE TECHNICAL CHEMISTS' HANDBOOK TABLE ?,— Continued. T. 'Snlphnr dioxide, 8. Hydrogen jbloride. Methane, W. a. «. ». 9- a. «■ 79-789 22-83 506-7 1 82-5 0-05563 0-003959 1 77-210 22-09 ... 1 0-05401 ! 0-003842 2 74-691 21-37 499-8 81-4 ■ 0-05244 0-003729 3 72-230 20-67 0-05093 0-003620 4 69-828 19-98 493-7 80-4 0-04946 0-003514 5 67-485 19-31 0-04805 0-003411 6 65-200 18-66 486-9 79-3 04669 0-003312 7 62-973 18-02 0-04539 0-003218 8 60-805 17-40 480-8 78-3 0-04413 i 0-003127 9 58-697 16-80 , 0-04292 0-003039 10 56-647 16-21 473-9 77-2 0-04177 0-002956 11 54-655 15-64 0-04072 0-002880 12 52-723 15-09 467-7 76-2 0-03970 0-002805 13 50-849 14-56 0-03872 0-002733 14 49-033 14-04 461-5 75-2 0-03779 0-002666 15 47-276 13-54 0-03690 0-002600 16 45-678 13-05 455-2 74-2 0-03606 0-002538 17 43-939 12-59 0-03525 0-002479 18 43-360 12-14 448-3 73-1 0-03446 0-002422 19 40-838 11-70 ... 0-03376 0-002369 20 39-374 11-29 442-0 72-1 0-03308 0-OOB319 21 37-970 10-89 0-03243 0-002270 22 36-617 10-50 435-0 71-0 0-03180 0-002223 23 35-302 10-13 0-03119 0-002178 24 34-026 9-76 428-7 70-0 0-03061 0-002134 25 32-786 9-41 0-03006 002092 26 31-584 9-07 423-0 69-1 0-02952 0-002051 27 30-422 8-43 ... 0-02901 0-002012 28 29-314 8-42 417-2 68-2 0-02852 0-001974 29 28-210 8-10 0-02806 0-901939 30 27-161 7-81 411-5 67-3 0-02762 0-001905 35 22-489 6-47 02546 0-001732 40 18-766 5-41 387-7 63-3 0-02369 0-001686 50 >■■ 361-6 59-6 0-02134 001359 60 •■• 338-7 56-1 0-01954 0-001145 70 ... ..• 0-01825 0-000926 80 ... ... ■ •• 0-01770 0-000695 90 ... .*• ••. 0-01735 0-000398 100 ... ... ... ... 0-01700 0-000000 SOLUBILITY OF GASES IN WATER TABLE 8— Continued. 21 Nitrous oxide, Ethylene, W. Acetylene, W. Air, W. in T. Alcohol, B. u. «■ .. S- u. u. 0-226 0-0281 1-73 0-20 0-02881 4-1780 1 0-219 0-0272 1-68 0-19 0-02808 4-1088 2 0-211 0-0262 1-63 0-19 0-02738 4-0409 3 0-204 0-0254 1-68 0-18 0-02670 3-9741 4 0-197 0-0245 1-53 0-18 0-02606 3-9085 5 0-191 0-0237 1-49 0-17 0-02543 3-8442 6 0-184 0-0228 1-45 0-17 0-02482 3-7811 7 0-178 0-0221 1-41 0-16 0-02424 3-7192 8 0-173 0-0214 1-37 0-16 0-02369 3-6585 9 0-167 0-0207 1-34 0-15 0-02316 3-5990 10 0-162 0-0200 1-31 0-15 0-02264 3-5408 n 0-157 0-0194 1-27 0-15 0-02217 3-4838 . 12 0-152 0-0188 1-24 0-14 0-02171 3-4?79 13 0-148 0-0183 1-21 0-14 0-02127 3-3734 14 0-143 0-0176 1-18 0-14 0-02085 3-3200 15 0-139 0-0171 1-15 0-13 0-02046 , 3-2678 16 0-136 0-0167 1-13 0-13 0-02005 , 3-2169 17 0-132 0-0162 1-10 0-13 0-01970 3-1672 18 0-129 0-0158 1-08 0-12 0-01935 , 3-1187 19 0-125 0-0153 1-05 0-12 0-01901 3-0714 20 0-122 0-0150 1-03 0-12 0-01869 3-0253 21 0-119 0-0146 1-01 0-12 0-01838 2-9805 22 0-116 0-0142 0-99 0-11 0-01808 2-9368 23 0-114 0-0139 0-97 0-11 0-01779 , 2-8944 24 0-111 0-0135 0-95 0-11 0-01751 2-8532 25 0-108 0-0131 0-93 0-11 0-01724 .. ■ 26 0-106 0-0129 0-91 0-10 0-01698 27 0-104 0-0126 0-89 0-10 0-01674 28 0-102 0-0123 0-87 0-10 0-01650 29 0-100 0-0121 0-85 0-10 0-01627 30 0-098 0-0118 0-84 0-09 0-01606 0-01503 0-01418 ... 0-01297 ... 0-01216 ... 0-01156 • •1 0-01126 ... ,. *>f .•• 0-01113 i " ... ... 0-01105 22 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 9.— SPEOIPIO GRAVITIES OF SOLIDS. Alumina, anhydrous . 4-15 Calcspar 2-72 Alum, ammonium 1-626 Cannel coal . 1-16-1 -27 potassium . 1-724 Cement 2-7-3-05 Aluminium sulphate, China clay, kaolin 2-21 cryst. 1-596 Charcoal, organic 1-57 Aluminium . 2-76 wood . 0-3-0 -5 Alum stone . 2-8 Coke, porous .0-4 Ammonium nitrate 1-707 Coal, porous 1-16-1-63 sulphate . 1-77 Copper, metallic, cast . 8-726 chloride . 1-528 hammered 8-94 Anhydrite (CaSOi) . 2-96 pyrites . 4-1-4-3 Anthracite . 1-4-1-7 oxide 6-43 Antimony . 6-7 sulphate 2-27 Arsenious acid 3-884 Cuprous sulphide 5-97 Arsenic acid 4-250 Clay .... 1-8-2-6 Asphalt 1-1-1-2 Cryolite 2-96 Ash wood . 0-7-0-8 Elm wood . 0-67 Barium chloride, cryst. 2-664 Fat, animal . 0-92 carbonate 4-56 Felspar 2-5-2-6 sulphate (spar) 4-73 Fibres, vegetable 1-51 hydroxide, cryst. 1'66 Fir wood, dry 0-6 Basalt .... 2-8-3-2 Firebricks . 1-85 Beech wood, dry . 0-7-0-8 Flint .... 2-7 Birch wood, dry . 0-7-0-8 Glass, green 2-642 Bismuth 9-85 plate 2-460 Borate of magnesium crystal, "Bohem. 2-9-3-0 (boracite) . 2-9 flint, English . 3 -4-3 -44 Borax, crystallised 1-692 Glauber's salt, cryst. . 1-52 Boric acid, crystallised 1-479 anhydrous 2-63 fused . 1-830 Granite 2-5-2 -9 Brown coal, lignite 1-2-1-4 Gypsum ,plaster-of-Paris 2-322 Brickwork . 1-5-1-7 cast, dry 0-97 Bricks, ordinary . 1-4-2-2 Heavy spar . 4-3-4-48 Brass . . . 8-4-8-7 Ice(0°). 0-917 Calamine 4-1-4-5 Iodine .... 4-948 Chalk .... 1-8-2-7 Iron, wrought 7-8-7-9 Calcium chloride, crys- grey, cast . 6-6-7-3 taUised 1-612 white, cast . 7-1-7-9 chloride, anhydrous 2-240 sesquioxide 5-22 silicate . 2-9 hydrated oxide . 3-94 carbonate 2-7 magnetic oxide . 5-4 phosphate 3-18 carbonate . 3-87 sulphate, anhydrous 2-927 sulphate, cryst. . 1-904 SPECIFIC GRAVITIES OF SOLIDS TABLE 9— Continued. 23 Iron pyrites, white 4-65-4-88 Potassium chloride . 1-945 pyrites . 5-18 chromate . 2-603 Ivory .... 1-83-1 -94 nitrate 2-058 Larch wood 0-44-0 -5 sulphate . 2-66 Lignite 1-2-1-4 bisulphate . 2-277 Lime, burnt, quick- . 3-08 hydroxide . 2-044 Lime wood . 0-5 Quartz 2-7 Litharge 9-36 Resin . 1-07 Lead, cast . 11-3 Rock salt . 2-1-2-2 red . 8-62 Sal-ammoniac 1-528 chromate . 6-00 Sand, dry . 1-4-1-6 acetate, cryst. . 2-395 damp 1-9-2-0 carbonate . 6-47 Sandstone . 1 •9-2-5 nitrate 4-40 Silver . 10-6 oxide 9-41 Silver chloride 5-501 sulphide . 7-505 Slate . 2-7 sulphate . 6-169 Sodium carbonate, anh. 2-509 chloride . 5-802 carbonate, cryst 1-454 | Magnesia, calcined . 3-2 chloride . 2-078 carbonate . 2-94 nitrate . 2-226 Magnesite . 2-9-3-1 sulphate . 2-63 Magnesium sulph.jCryst . 1-751 sulphide . 2-471 chloride, cryst 1-558 thiosulphate . 1-736 Manganese peroxide . 2-94 hydroxide 2-130 native ore .4-7-5.-0 Steel .... 7-80 Maple wood 0-5-0-6 Steel, cast . 7-92 Marble 2-5-2-8 hardened . 7-66 Nickel 8-9 Sulphur, native . 2-069 Oak, dry . 0-85-0-95 sticks, fresh . 1-98 Phosphorus, yellow . 1-826 sticks, old 2-05 red 2-106 soft, amorphous 1 -96 | Pine wood, white 0-55 Sulphuric anhydride . 1-97 red . 0-5 Tin, cast . 7-21-7-4 Platinum . 21-1 hammered 7-475 Pock wood . 1-263 Willow wood" 0-5-0-58 Poplar 0-38 Witherite . 4-30 Porcelain 2-1-2-5 Zinc, cast . 6-8 Porphyry . 2-8 rolled . 7-2 Potash, natural . 2-3 blende 3-9-4-2 Potassium carbonate . 2-264 oxide . 5-73 chlorate 2-35 sulphate 2-036 24 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 10.— WEIGHT OP SUBSTANCES AS STORED. 1 Cubic 1 Cubic Tons Substance. Metre Foot per Weighs Weiglia Cub. root. Kilo. lb. avdp. Bricks 2100 131 ■0584 Cement 120"0 75 ■0335 Clay, damp 1650 103 •0459 dry 1570 98 •0437 Limestone and other building stones . 2000 125 ■0558 Mortar (lime and sand) 1800 112 •0500 Quicklime 1000 62-5 ■0279 Sand, dry 1330 83 •0370 damp 1770 110 •0491 Wood, beech logs .... 400 24-5 •0107 fir logs 330 20-5 •0091 oak logs 420 26 •0116 Raw Materials, etc., for Alkali Works. Pyrites, broken pieces 2500 156 •0696 smalls 2340 146 -5 •0654 1520 95-0 •0424 Nitre 1310 81-5 ■0364 1335 83 •0375 Salt 689 43 •0192 Saltcake 1180 73-5 •0328 Limestone (small pieces) . 1400 87-5 •0391 962 60 •0268 Alkali waste (wet) .... Soda salts (NaaCOs + HaO) (drained) . 1268 79 •0352 810 50-5 •0225 Soda ash (ungrouiw) . . ' . 1195 74-5 •0332 Soda crystals 1010 63 •0281 Bicarbonate (ground) .... 986 61-5 •0274 Sieved lime (for bleaching powder) . 1058 66 •0295 497-593 31-37 •0151 721-834 45-52 •0216 Manganese dioxide, native 2210 138 •0616 Limestone dust . . . . - . 1550 96-5 •0431 Coke (for filling towers) 417-534 26-33 •0131 Flints „ „ ... 1600 100 ■0446 Cinders (ashes) 738 46 0205 SPECIFIC GRAVITY OF LIQUIDS, ETC. 25 TABLE 11.— SPBOIPIO GRAVITY OP LIQUIDS. Acetic anhydride Acetone .... Alcohol .... Acetic acid Bisulphide of carbon Benzene .... Coal tar .... Ether .... Glycerine .... Linseed oil . . . Mercury .... Nitrogen peroxide (liquid) Olive oil . Petroleum Rapeseed oil . Sulphur dioxide (liquid) . Sea-water Spirits of turpentine Specific Gravity. 1-004 0-81 0-7939 1-064 1-272 0-884 1-15 0-723 1-260 0-9347 3-596 1-45 0-917 0-78-0-81 0-9136 1-45 1-02-1-04 0-865 Temp. 17° 12° -5 17° 15° -5 15° 12° -5 15° 15° 0° 15° 15° 15° 20° 15° 15° TABLE 12.— SPECIPIO GRAVITY AND PERCENT- AGE OP SOLUTIONS SATURATED AT 15°. The percentage refers to Anhydrous Salt in 100 solution. Tem- Percentage Specific Degrees perature. of Salt. Gravity. Twaddell. Ammonium chloride 15 26-30 1-0776 15-5 sulphate 19 50-00 1-2890 57-8 Barium chloride 15 25-97 1-2827 56-5 Calcium chloride . 15 40-66 1-4110 82-2 Magnesium sulphate 15 25-25 1-2880 57-6 Potassium chloride . 15 24-90 1-1723 34-4 carbonate 15 52-02 1-5708 114 nitrate , 15 21-07 1-1441 28-8 sulphate 15 9-92 1-0831 16-6 Sodium chloride 15 26-395 1-2043 40-8 carbonate . 15 14-35 1-1535 30-7 nitrate 19-5 46-25 1-3804 76 sulphate . i 15-0 1 11-95 1-1117 22-3 26 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 13.— LINEAR EXPANSION OP SUBSTANCES. By heating from 0° to 100° C. (32°-212° F.). Aluminium . Brass . Bronze Charcoal from oak fir Copper Glass, flint . white green Gold . Iron, wrought cast . Lead . Marble of Carrara St Beat Mercury Nickel Platinum Porcelain (Berlin) Silver . Solder, hard Steel, hardened . not hardened Tin . Water . Zinc . 0-00218 459 0-001982 535 0-001820 549 0-001200 833 0-00100 1000 0-001714 582 0-000817 1219 0-000861 1161 0-000766 1 1305 0-001431 1 682 0-001235 812 0-001144 901 0-002938 351 0-000849 1178 0-000418 2392 0-0182 55 0-001516 600 0-000884 1132 0-000336 3000 0-001954 524 0-002058 486 0-001240 807 0-001079 927 0-002703 516 0-015538 71-4 0-001711 :340 I ^(N OOCDtHN OOeOTfltN O0yTt<-t^t^J>.00QD00Q0000i0S030i0i0SOOOOOi— li-H rHi-HiHi-(rHrHrHTHT-(i-(r-(i-Hi-lrHi-Hi-(-OOOOOiOiHC<)C-OD010 + OOCDtWCT 00<0"^(N C30?D^(M OQi^-^C^ OOCD + O0(O-^C- oo Cft o O i^ (N w • (M iM (M « (N 00Oi-IC0u^l>-01O(MT*iC0Q0a)iHC0iiOI>-00O{N4fi5DJ>- t**Tjii0iOlO10Oi0CD«>CDC0C0«Dt-l>.J>-r>-t-00Q0000000 + ■yH CT 00 ep "^ (N 00 cp "jH cq op y ^ CN 00 CO -^ (N oo (O^OOOOOiOiHCqWCO-^lOCOCDlr^OOOiOOf^iMM-^-^ _^ r-t iH iH i-H »-< t-H i-t iH iH i-H i-H rH Cq CM dCO (MTtl^oO (M-^^cp (M^Jfcooo (M-^rfi ooocoTji(M)-ioai>.w5CO(MooocO"^co.^Oii?»o-#(rqoi^ ■^COCOCOCOCO(MCT(M(M(?qCMrHi-(.-trH,-( j_ _l ]*" (M -jH «• CO (M -Jf "p oo (M -^ I© oo (M -^ « 00 CM tH -5D\ir5'^THco(Mi-HOOoaooi>.cocojJ:s4t-COO-^CO(Mr-< OOaQOI>i TtOi-iMeo^ioot-oooiOi-tc^oo^iotot-ooo>Oi-H(Na3-^»ottib-c»«owci t-J^Jt-000000C000C0Q0000000aiai0>C10a01Csei0i0»OOOOOOOOOOi-lrHrH i-lrHrHrHr-lr-lt-HrHrHr-li-lr-lrHi-D3QOc4£~i-tcoo^o>cocod£->-4«oO'^aacoooc4f-iHeoo !qoococ»^otOl-4£-cqcoooo>■^o-l^-c^QOcoa^^o j ^oo■Ht-c4-;4^ + ^r-(i-lr-lrHr-eooocqb-i--(00-«o>eociocmco<^*t>-r-t^o o■--l±-C4ooeQ03■^ocOl-HW<^]coMO>'^p^>H^-l^l»«o>■^o^l74^-cq<»mo»^ Oi^i^C4C4mo3-^iaia^Q?J>^raDo6iOOi-Oi-Ht-COC»Or-IINOO'*»0«Dt*00010r-tMei3-*iOfflb-CO. ■*oeoMc^t-I-^^oo■*OlOTcpOTt-lH(po■*olm(»«^-.J^oo■*»«»«^-I-l«po I + HC4C4IMC4cacOC4l!>r-lp0^eaOOCOC4^-iHcpp^acpCIDC4t-r-l«0 rf!eo«mmo3mcom«moQeQeou303GOooooc4Me4e4c4e4(Ne4e4-OOOOOOOOOt*iOCOrHO i-iC^-^i-fi-HiHrHTHrHrHi-l tH 60 S 60.9 ^~. a a bo . . 'S 'E . "p. 5,3 " & 2 I CQ d o o t^ C^ 5 B u a.g 1h &o^ I Si .a a^ . 3 ^^S CO CO CO CO CO M CO y ^^ rrt S'S o o o o o o o ^ « o •SS.2 Vi B So Pi 3 SS-3 S » ^1 .as 3 u fclOJ i-l (3 S r-1 i-H r-l iH iftOi«w^o"■'' " S J3 ^^ V >,% O o g T3 g-^i) ;a u 60 bo 6D± -S & a 'S !i) 60 .s o » «=2 S "Zh 3 S a 3 g g m m.a a B B s- s s a ° S U Jj u TABLE 20.— REDUCTION OP THE VOLUME OP Vx278!> General formula for Diy Gases, Vq &=Baroinetric pressure, reduced to 0' (273+()760 t= temperature; /= tension I. Table for reducing the volumes of 0°. 1°. r. 3°. 4". 5% 6°. 7". 8'. 9". 10°. 0*. 1 0-996 0-993 0-989 0-986 0-982 0-978 0-975 0-972 0-968 0-966 1 2 1-993 1-986 1-978 1-971 1-964 1-957 1-960 1-948 1-986 1-929 2 3 2-989 2-978 2-967 2-967 2-946 2-936 2-925 2-915 2-904 2-894 8 4 3-985 3-971 3-956 3-942 3-928 3-914 3-900 3-886 3-872 3-869 4 5 4-982 4-964 4-946 4-928 4-910 4-893 4-876 4-868 4-841 4-824 6 6 6-978 6-956 6-985 5-913 6-892 5-871 5-850 6-880 6-809 6-788 6 7 6-974 6-949 6-924 6-899 6-874 6-860 6-826 6-801 6-777 6-753 7 8 7-970 7-942 7-913 7-885 7-856 7-828 7-800 7-773 7-746 7-718 8 9 8-967 8-934 8-902 8-870 8-838 8-807 8-775 8-744 8-n3 8-682 9 10 9-963 9-927 9-891 9-856 9-820 9-786 9-750 9-716 9-681 9-647 10 11 10-96 10-92 10-88 10-84 10-80 10-76 10-73 10-69 10-65 10-61 11 12 11-96 11-91 11-87 11-83 11-78 11-74 11-70 11-66 11-62 11-67 12 13 12-95 12-91 12-86 12-81 12-76 12-72 12-68 12-63 12-69 12-54 13 14 13-95 13-90 13-86 13-80 13-75 13-70 13-66 13-60 18-65 13-60 14 15 14-95 14-89 14-84 14-78 14-78 14-68 14-63 14-67 14-52 14-47 16 16 16-94 15-88 16-88 15-77 16 -n 15-66 15-60 15-65 15-49 16-43 16 17 16-94 16-87 16-82 16-76 16-69 16-64 16-68 16-62 16-46 16-40 17 18 17-93 17-87 17-81 17-74 17-67 17-61 17-65 17-49 17-43 17-36 18 19 18-93 18-86 18-79 18-72 18-66 18-59 18-53 18-46 18-39 18-33 19 20 19-98 19-86 19-78 19-71 19-64 19-67 19-50 19-43 19-36 19-29 20 21 20-93 20-84 20-77 20-69 20-62 20-66 20-48 20-40, 20-33 20-26 21 22 21-92 21-84 21-76 21-68 21-60 21-63 21-46 21-37 21-80 21-22 22 23 22-92 22-83 22-75 22-66 22-68 22-61 22-43 22-35 22-26 22-18 23 24 23-92 28-82 28-74 23-65 23-66 23-48 28-40 23-32 23-23 23-15 24 25 24-91 24-81 24-73 24-64 24-56 24-46 24-38 24-29 24-20 24-11 25 26 25-91 25-81 25-72 25-62 26-63 25-44 25-35 25-26 26-17 25-08 26 27 26-90 26-80 26-71 26-61 26-62 26-42 26-33 26-23 26-13 26-04 27 28 27-90 27-79 27-69 27-59 27-50 27-40 27-30 27-20 27-10 27-01 28 29 28-90 28-78 28-68 28-68 28-48 28-38 28-28 28-17 28-07 27-97 29 30 29-89 29-78 29-67 29-67 29-46 29-36 29-25 29-15 29-04 2S-94 80 31 30-89 80-77 30-66 30-65 30 44 80-84 30-28 30-12 30-01 29-91 81 82 31-88 31-76 31-65 81-54 31-42 31-32 31-20 31-09 30-98 80-87 32 83 S2-8S 82-76 82-64 82-52 32-40 82-80 82-18 32-06 31-94 81-84 38 34 33-88 38-76 83-68 33-61 88-83 88-27 33-16 33-08 32-91 82-80 34 35 34-87 84-74 84-62 84-50 34-37 84-25 34-13 34-01 33-88 33-77 85 36 86-87 36-74 86-61 36-48 85-85 85-23 85-10 34-98 84-86 34-78 36 87 86-87 36-73 36-60 86-47 36-83 86-21 36-08 35-95 86-82 35-70 37 38 37-86 37-72 37-69 37-45 87-32 S7-19 87-05 36-92 86-79 36-66 88 39 38-85 38-71 88-68 38-44 88-30 88-16 88-03 37-89 37-76 37-62 89 40 39-86 39-71 89-66 89-42 39-28 39-14 89-00 38-86 38-72 38-69 40 41 40-85 40-70 40-65 40-41 40-26 40-12 39-98 39-88 89-69 39-65 41 42 41-85 41-69 41-64 41-39 41-24 41-10 40-95 40-80 40-66 40-52 42 43 42-84 42-68 42-63 42-38 42-22 42-08 41-93 41-78 41-62 41-48 43 44 43-84 43 '68 43-62 43-87 48-20 48-06 42-90 42-76 42-69 42-45 44 45 44-84 44-67 44-61 4435 44-19 44-08 43-88 43-72 43-66 43-41 45 46 45-83 45-66 45-50 46-34 45-17 46-01 44-85 44-69 44-63 44-38 46 47 46-88 46-66 46-48 46 32 46-16 46-99 45-83 46-66 45-60 45-34 47 48 47-88 47-65 47-48 47-31 47-13 46-97 46-80 46-68 46-47 46-81 48 49 48-82 48-64 48-47 48-29 48-12 47-95 47-78 47-60 47-44 47-27 49 50 49-82 49 64 49-46 49-28 49-10 48-98 48-75 48-58 48-41 48-24 50 GASES TO NORMAL TEMPERATURE & PRESSURE. General formula for Moist Gases, Vo = yx^^^Ct-/) ' " (273+0700 of aqueous vapour at f. Compare Table 23. gases to a temperature of 0° C. 0\ 1". 2". 3". 4". 5". 6'. 7-. S°. 9°. 10'. O". 51 50-82 50-63 50-46 50-26 60-08 49-91 49-73 40-56 49-38 49-21 61 52 51-81 51-62 51-44 61-26 61-06 60-89 60-70 60-62 60-35 50-17 52 53 52-81 52-62 62-43 62-24 52-06 61-87 61-68 51-49 61-31 51-13 53 54 63-81 53-61 63-42 63-22 63-03 52-84 52-66 52-46 52-28 62-10 54 55 54-80 51-60 64-41 64-21 54-01 63-82 53-63 53-44 63-25 63-06 55 56 65-80 56-60 55-40 55-19 54-99 54-80 54-60 54-41 64-22 54-03 66 57 56-80 66-60 56-30 56-18 66-97 56-78 56-68 55-38 65-19 54-99 57 58 57-79 67-58 57-37 6716 66-96 66-76 66-55 66-36 56-15 65-96 58 50 68-79 68-57 58-37 68-15 57-93 57-74 67-63 67-32 57-12 56-92 59 60 60-78 69-66 60-35 59-13 58-92 58-71 58-50 58-30 68-09 57-88 60 61 60-78 60-56 60-34 60-12 69-90 59-69 50-48 69-27 59-06 68-86 61 62 61-78 61-65 61-33 61-10 ■ 60-88 60-67 60-45 60-24 60-03 69-81 62 63 62-77 62-64 62-32 62-09 61-86 61-65 61-43 61-21 60-99 60-77 63 64 63-77 63-53 63-31 63-07 62-84 62-63 62-40 62-18 61-96 61-74 64 65 64-76 64-53 64-30 64-06 63-83 63-61 63-38 63-16 62-93 62-70 66 66 65-76 66-62 65-20 65-04 64-81 64-68 64-36 6413 63-89 68-67 66 67 66-75 66-61 66-27 66-03 65-79 65-66 66-33 66-10 64-86 64-63 87 es 67-75 67-50 67-26 67-02 66-77 66-64 66-30 66-07 65-83 65-60 68 60 68-75 68-60 68-25 68-01 67-75 67-52 67-28 67-04 66-80 66-56 09 70 69-74 69-49 69-24 68-99 68-74 68-60 68-26 68-01 67-77 67-53 70 71 70-74 70-48 70-23 69-98 69-72 69-48 69-23 63-98 68-74 68-49 71 72 71-74 71-48 71-22 70-06 70-70 70-46 70-20 69-96 69-71 69-46 72 73 72-73 72-47 72-21 71-95 71-69 71-44 71-18 70-93 70-67 70-42 73 74 73-73 73-46 73-20 72-93 72-66 72-41 72-16 71-90 71-64 71-39 74 75 74-72 74-45 74-19 73-92 73-66 73-39 73-13 72-87 72-61 72-36 75 76 75-72 76-45 75-18 74-90 74-63 74-37 74-10 73-84 73-58 73-32 76 77 76-72 76-44 76-17 75-89 75-61 76-35 76-08 74-81 74-66 74-28 77 78 77-71 77-48 77-16 70-87 76-69 76-33 76-05 75-78 76-51 75-25 78 79 78-71 78-42 78-14 77-86 77-58 77-31 77-03 76-76 76-48 76-21 79 80 70-ro 79-42 79-13 78-85 78-56 78-28 78-00 77-73 77-45 77-18 80 81 80-70 80-41 80-12 79-83 79-54 79-26 78-98 78-70 78-42 78-14 81 82 81-69 81-40 81-n- 80-82 80-52 80-24 79-05 79-67 79-39 79-11 82 83 82-69 82-39 82-10 81-81 81-61 81-22 80-93 80-64 80-36 80-07 83 84 83-69 83-39 83-09 82-79 82-49 82-20 81-90 81-61 81-32 81-04 84 85 84-68 84-38 M-08 83-78 83-47 83-17 82-88 82-63 82-29 82-00 85 86 85-68 85-37 85-07 84-76 84-46 84-16 83-86 83-65 83-26 82-97 80 87 86-68 86-37 86-06 86-76 86-43 85-13 84-83 84-63 84-23 83-93 87 88 87-67 87-36 87-05 86-73 86-42 86-11 86-80 86-60 85-20 84-90 88 80 88-67 88-36 88-04 87-72 87-40 87-09 86-78 86-47 86-16 86-86 89 00 89-67 89-34 89-02 88-70 88-38 88-07 87-76 87-44 87-13 80-82 00 91 90-66 90-34 90-01 89-69 89-36 89-06 88-73 88-41 88-10 87-79 91 92 91-66 91-33 91-00 90-67 90-34 90-03 89-70 89-33 89-07 88-75 92 93 92-66 92-32 91-99 91-66 91-83 91-01 9008 90-36 90-03 89-72 93 04 93-65 93-31 92-98 92-64 92-31 91-98 91-65 91-33 91-00 90-08 94 95 94-66 94-31 93-97 93-63 93-29 92-96 92-63 92-30 91-97 91-65 95 96 95-65 S5-S0 94-96 94-61 94-27 93-94 9S-60 93-27 92-94 92-61 96 97 96-64 96-29 96-95 95-60 95-26 94-92 94-58 94-24 93-91 93-57 97 98 97-64 97-28 96-93 96-58 96-24 95-00 95-56 95-21 94-87 94-54 98 go 98-64 98-27 97-92 97-57 97-22 96-87 96-53 96-18 96-84 96-60 90 100 90-63 90-27 08-91 98-56 98-20 97-85 97-60 97-10 96-61 06-47 100 38 THE TECHNICAL CHEMISTS* HANDBOOK TABLE 20— I. Table for reducing the volumes of 0*. 11°. 12°. 13". 14". 15°. 16°. 17". 18'. 19°. 20°. 0°. 1 0-961 0-958 0-955 0-951 0-948 0-946 0-941 0-9S8 0-935 0-932 1 2 1-923 1-916 1-909 1-903 1-896 1-889 1-883 1-876 1-889 1-864 2 3 2-834 2-874 2-864 2-854 2-844 2-M4 2-824 2-815 2-805 2-796 3 4 3-845 3«32 3-818 3-806 3-792 3-779 3-766 3-763 3-740 3-727 4 5 4-807 4-790 4-773 4-767 4-740 4-724 4-707 4-691 4-676 4-869 6 6 6-768 6-747 5-728 6-708 5-688 5-668 6-648 5-629 6-609 5-591 6 1 6-729 6-705 6-682 8-659 6-636 6-613 6-590 6-667 6-544 6-523 7 8 7-690 7-663 7-637 7-610 7-684 7-658 7-531 7-606 7-479 7-454 8 9 8-652 8-621 8-591 8-562 8-532 8-602 8-472 8-444 8-414 8-386 9 10 9-613 9-579 9-546 9-513 9-480 9-447 9-414 9-S82 9-349 9-318 10 - 11 10-67 10-63 10-60 10-46 10-43 10-39 10-36 10-32 10-28 10-25 11 12 11-63 11-49 11-45 11-42 11-38 11-33 11-30 11-26 11-21 11-18 12 13 12-49 12-45 12-41 12-36 12-32 12-28 12-24 12-20 12-16 12-11 13 M 13-45 13-41 13-36 13-31 13-27 13-22 18-17 13-13 13-08 13-04 14 15 14-42 14-37 14-32 14-27 14-22 14-17 14-12 14-07 14-02 13-97 15 16 15-38 16-32 16-27 16-22 16-17 15-n 16-06 15-01 14-96 14-91 18 17 16-34 16-28 16-23 16-17 16-12 16-08 16-00 16-96 16-89 15-84 17 18 17-30 17-24 17-18 17-12 l7-0li 17-00 18-94 16-89 16-82 16-78 IS 19 18-26 18-20 18-14 18-07 18-01 17-96 17-89 17-83 17-76 17-70 19 20 19-23 19-16 19-09 19-03 18-96 18-89 18-83 18-76 18-69 18-64 20 21 20-19 20-12 20-04 19-98 19-91 19-84 19-77 19-70 19-62 19-57 21 22 21-15 21-08 21-00 20-93 20-86 20-78 20-71 20-64 20-56 28-60 22 • 23 22-11 22-03 21-95 21-88 21-80 21-73 21-66 21-68 21-60 21-43 23 24 23-07 22-99 22-01 22-83 22-76 22-07 22-69 22-51 22-43 22-37 24 25 24-03 23-95 23-86 23-78 23-70 23-61 23-54 23-45 23-37 23-30 25 26 25-00 24-91 24-81 24-73 24-65 24-56 24-48 24-39 24-30 24-23 28 27 25-96 26-87 25-77 25-09 25-60 25-60 25-42 25-33 26-23 25-16 27 28 26-92 26-82 26-72 26-64 26-64 26-46 26-36 26-27 26-17 26-09 28 29 27-88 27-78 27-68 27-69 27-49 27-39 27-80 27-20 27-10 27-02 29 30 28-84 28-74 28-64 28-54 28-44 28-34 28-24 28-15 28-05 27-95 30 31 29-80 29-70 29-59 29-49 29-39 29-28 29-18 29-09 28-99 28-87 31 32 30-76 30-66 30-56 30-44 80-34 30-23 30-12 30-03 29-92 29-81 32 33 31-72 31-61 81-60 31-39 31-28 31 -IT 31-06 30-97 30-86 30-74 33 34 32-68 32-57 32-46 32-34 32-23 3212 32-»l 31-90 31-79 31-68 34 35 33-65 33-63 33-41 83-30 33-18 33-06 32-95 82-84 32-73 32-61 35 36 34-61 34-49 34-37 34-25 34-13 34-01 33-89 33-78 33-66 33-64 36 37 35-57 35-46 36-32 36-20 35-08 34-95 34-83 34-72 34-59 34-47 37 38 36-63 36-40 36-28 36-15 36-02 36-90 35-77 36-66 35-53 36-40 38 39 37-49 37-36 87-23 37-10 36-97 86-84 36-71 36-69 36-46 36-34 39 40 38-45 38-32 38-18 33-05 37-92 37-79 37-66 37-63 37-40 37-27 40 41 89-41 89-28 39-14 39-00 38-87 38-73 38-60 38-47 38-34 38-20 41 42 40-37 40-24 40-09 39-95 39-82 39-68 39-54 39-41 39-27 39-18 42 43 41-33 41-19 41-06 40-90 46-76 40-62 40-48 40-36 40-21 40-»7 43 44 42-30 42-15 42-00 41-86 41-71 41-57 41-43 41-28 41-14 41-00 44 45 43-26 43-11 42-95 42-81 42-66 42-51 42-37 42-22 42-08 41-93 46 46 44-29 44-07 43-91 43-76 43-61 43-40 43-31 43-16 43-01 42-86 46 47 46-18 45-08 44-86 44-71 44-56 44-40 44-25 44-10 43-94 43-79 47 48 46-14 45-98 45-82 45-66 45-50 45-35 45-19 45-04 44-88 44-72 48 49 47-10 46-94 46-77 46-61 46-45 46-29 46-13 45-97 45-81 45-86 49 50 48-07 47-90 47-73 47-67 47-40 47-24 47-07 46-91 46-75 46-69 60 REDUCTION OF THE VOLUME OF GASES 39 Gontinimd. gases to a temperature of 0° C. — Continued. 0'. 11". 12'. 13°. 14'. 15'. 16*. 17'. 18". 19'. 20-. 0". 61 49-08 48 -86 48-69 48-62 48-35 48-lS 48-01 47-85 47-68 47-62 61 62 49-99 49-12 49-64 49-47 49-30 49-13 48-96 4J-79 48-62 4S-46 52 63 60-96 60-77 66-69 60-42 60-24 58-07 49-89 49-72 49-66 49-38 63 64 51-91 61-73 61-56 61-37 51-19 61-02 60-54 60-66 60-49 60-82 64 66 62-87 62-69 62-60 52-33 62-14 61-96 61-78 61-60 61-43 61-25 66 66 63-84 63-66 63-46 63-28 63-09 62-91 52-72 52-64 62-36 62-18 66 67 54-80 64-61 64-41 64-28 54-04 53-86 63-66 63-48 63-29 53-71 67 68 *5-76 66-66 66-37 65-18 64-98 64-80 64-80 64-42 54-23 54-04 58 69 66-72 56-62 66-32 66-13 66-93 56-74 66-54 65-36 56-16 64-97 59 60 67-68 67-47 67-28 67-88 56-88 66-68 66-48 66-29 56-09 66-91 60 61 58-64 68-43 68-23 68-03 67-83 57-63 67-42 67-23 57-02 66-84 61 62 69-60 69-39 69-19 68-98 68-78 68-57 58-36 68-17 67-96 67-77 62 63 60-66 60-36 60-14 69-93 59-72 59-52 69-30 69-11 68-90 68-71 63 64 61-63 61-31 01-10 60-88 68-07 66-46 06-25 60-04 69-83 59-64 64 65 62-49 62-26 62-06 61-84 61-62 61-40 61-19 60-98 60-77 60-67 65 66 63-46 63-22 63-01 62-79 62-67 62-35 62-13 61-92 61-70 61-50 66 67 64-41 64-18 63-96 63-74 63-62 63-29 63-07 62-86 82-63 62-43 67 68 65-37 65-13 64-92 «4'69 64-46 64-23 64 01 63-80 63-57 63-36 68 69 66-33 66-09 66-87 66-64 66-41 65-18 64-96 64-73 64-60 64-30 69 70 67-29 67-06 66-82 66-69 66-36 66-13 66-90 66-67 65-44 65-23 70 71 68-25 68-01 67-77 67-54 67-31 67-07 66-84 66-61 66-38 66-16 71 72 69-21 S8-97 68-73 68-49 68-26 68-02 67-78 67-66 67-31 67-09 72 78 70-17 69-92 69-68 69-44 69-20 68-96 68-72 68-49 68-26 6803 73 74 71-14 70-88 79-64 70-48 78-15 69-91 69-66 69-42 69-18 68-96 74 76 72-10 71-84 71-69 71-36 71-10 70-86 70-61 70-37 70-12 69-89 75 76 73-06 72-80 72-65 72-30 72-05 71-80 71-65 71-30 71-06 70-82 76 77 74-02 73-76 73-61 73-26 73-80 72-74 72-49 72-24 71-98 71-75 77 78 74-98 74-71 74-46 74-20 73-94 73-69 73-43 73-18 72-92 72'«> 78 79 75-94 75-67 75-41 75-15 74-89 74-63 74-37 74-11 73-86 73-61 79 80 76-90 76-63 76-37 76-10 75-84 75-68^ 75-31 75-06 74-79 74-64 80 81 77-86 77-69 77-32 77-05 70-79 76-62 76-26 76-00 76-73 76-47 81 82 78-82 7S-66 78-28 78-00 77-74 77-47 77-19 76-94 76-66 76-40 82 88 79-78 80-76 79-60 79-23 75-95 78-68 78-41 78-13 77-87 77-60 77-34 83 84 80-46 8«-19 79-91 79-63 70-36 79-08 78-81 78-63 78-27 84 86 SI -71 81-42 81-14 80-86 80-68 80-30 80-02 79-76 79-47 79-20 86 86 82-67 83-63 84-69 86-66 86-62 82-38 82-10 81-81 81-63 81-24 80-96 80-69 80-40 80-13 86 87 83-33 83-06 82-76 82-48 82-19 81-90 81-63 81-38 81-06 87 88 84-29 84-01 83-71 83-42 83-13 82-84 82-67 82-27 81-99 88 89 86-25 84-96 84-66 84-37 84-08 83-78 83-60 83-22 82-93 89 90 86-21 85-92 85-62 85-32 85-02 84-72 84-44 84-14 83-86 90 91 87-48 88-44 89-40 90-36 91-33 87-17 86-87 86-57 86-27 86-96 86-66 86-38 85-07 84-79 91 92 88-13 87-83 87-52 87-22 86-91 86-60 86-32 86-01 85-72 92 93 39 -03 88-78 88-47 88-16 87-86 87-64 87-26 86-95 86-66 93 94 90-84 89-73 89-42 8911 88-80 88-49 8S-19 87-88 87-69 94 96 91-80 90-68 90-38 90-06 89-74 89-43 89-13 88-82 88-52 95 96 92-29 93-25 94-21 96-17 06-13 91-96 91-64 91-83 91-01 90-69 90-37 90-07 89-75 89-46 96 97 98 99 92-92 92-59 92-28 91-96 91-63 91-31 91-00 90-68 90-38 97 93-t7 93-56 93-23 92-90 92-58 92-26 91-94 91-62 91-31 98 94-83 94-60 94-18 93-85 93-62 93-19 92-88 92-65 92-24 99 96-79 96-46 96-13 94-80 94-47 94-14 93-82 93-49 93-18 100 40 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 20— I. Table for reduciDg the volumes of 0°. 21°. 22". £3». 24*. 25-. 26". 27-. 28'. 29°. 0'. 1 0-929 0-926 0-922 0-919 0-916 0-913 0-910 0-907 0-904 1 2 1-857 1-861 1-846 1-839 1-832 1-826 1-820 1-814 1-808 2 3 2-786 2-777 2-767 2-768 2-749 2-739 2-730 2-721 2-712 8 4 3-714e 3-702 3-690 8-677 3-665 3-652 3-640 8-628 3-616 4 5 4-643 4-628 4-612 4-597 4-681 4-666 4-561 4-636 4-620 5 6 6-672 5-553 5-534 6-516 5-497 5-479 5-461 5-442 S-424 6 7 6-600 6-479 6-457 6-435 6-413 6-392 6-871 6-349 6-828 7 8 7-429 7-404 7-379 7-354 7-830 7-305 7-281 7-256 7-282 8 9 8-357 8-830 8-302 8-274 8-246 8-218 8-191 8-163 8-186 9 10 9-286 9-255 9-224 9-193 9-162 9-131 9-101 9-070 9-040 10 11 10-21 10-18 10-16 10-11 10-07 10-04 10-01 9-98 9-94 11 12 11-14 11-11 11-07 11:03 10-99 10-96 10-92 10-88 10-86 12 13 12-07 12-03 11-99 11-96 11-91 11-87 11-83 11-79 11-75 13 14 13-00 12-96 12-91 12-87 12-83 12-78 12-74 12-70 12-66 14 15 13-93 18-88 13-84 13-79 13-74 13-70 13-65 , 13-61 18-66 16 16 14-86 14-81 14-76 14-71 14-66 14-61 14-66 14-61 14-46 16 17 15-79 15-73 15-68 15-63 15-58 16-62 15-47 15-42 16-37 17 18 16-71 16-66 16-60 16-55 16-49 16-44 16-88 16-33 16-27 18 19 17-6* 17-68 17-68 17-47 17-41 17-86 17-29 17-23 17-18 19 20 18-57 18-61 18-45 18-39 18-32 18-26 18-20 18-14 18-08 20 21 19-50 19-43 19-37 19-31 19-24 19-17 19-11 19-05 18-98 21 22 20-43 20-86 20-29 20-28 20-16 20-09 20-02 19-96 19-89 22 23 21-36 21-29 21-21 21-15 21-07 21-00 20-98 20-86 20-79 23 24 22-28 22.-21 22-14 22-07 21-99 21-91 21-84 21-77 21-70 24 25 23-21 23-14 23-06 22-99 22-90 22-83 22-76 22-68 22-60 25 26 24-14 24-06 23-98 28-91 23-82 28-74 28-66 23-58 23-50 26 27 25-07 24-99 24-90 24-88 24-73 24-66 24-67 24-49 24-41 27 28 26-00 25-91 25-82 25-74 25-65 25-67 25-48 25-40 26-81 28 29 26-93 26-84 26-75 26-67 26-67 26-48 26-39 26-30 26-22 29 30 27-86 27-77 27-67 27-68 27-49 27-39 27-80 27-21 27-12 80 81 28-79 28-70 28-59 28-50 28-41 28-30 28-21 28-12 28-02 81 32 29-72 29-62 29-51 29-42 29-32 29-22 29-12 29-02 28-93 32 S3 30-65 30-56 30-44 30-84 30-24 30-18 30-08 29-93 29-83 38 34 81-67 31-47 31-86 81-26 31-16 31-04 80-94 30-84 30-74 34 35 82-50 32-40 82-28 32-18 32-07 81-96 31-85 31-76 81-64 35 36 33-43 33-82 33-20 38-10 82-99 32-87 32-76 82-66 82-54 86 37 34-86 34-26 84-12 34-02 83-90 83-78 38-67 33-66 33-46 37 88 85-29 35-17 35-05 84-98 34-82 34-70 84-68 34-47 84-85 88 89 86-22 36-10 35-97 35-85 86-74 85-61 35-49 86-47 86-26 39 40 3r-14 37 02 36-90 36-77 36-65 36-52 36-40 36-28 36-16 40 41 8807 87-95 37-82 37-69 37-57 87-43 37-81 87-19 37-06 41 42 39-00 88-87 38-74 88-61 38-48 38-86 88-22 88-09 37-97 42 48 39-93 39-80 39-66 39-53 39-40 89-26 89-13 89-00 38-87 48 44 40-85 40-72 40-59 40-45 40-32 40-17 40-04 39-91 89-78 44 45 41-78 41-65 41-51 41-37 41-23 41-09 40-95 40-82 40-68 45 46 42-71 42-57 42-48 42-29 42-16 42-00 41-86 41-72 41-68 46 47 43-64 43-60 48-85 43-21 43 06 42-91 42-77 42-63 42-49 47 48 44-67 44-42 44-27 44-12 43-98 48-88 43 68 43-64 43-39 48 49 45-60 45-85 4519 45-04 44-89 44-74 44-59 44-44 44-30 49 60 46-43 46-28 4612 46-97 46-81 46-66 46-51 45 35 45-20 50 REDUCTION OF THE VOLUME OF GASES 41 Continued. gases to a temperature of 0° C. — Contimued. 0°. 21°. 22-. 23'. 24". 25°. 26°. 27°. 23°. 29°. 0°. 61 47-36 47-20 47-04 46-89 46-73 46-57 46-42 46-26 46-10 51 52 48-29 48-13 47-96 47-31 47-64 47-49 47-33 47-16 47-01 52 63 49-22 49-06 48-89 48-78 48-66 48-40 48-24 48-07 47-91 63 61 50-14 49-98 49-81 49-66 49-43 49-31 49-15 48-98 48-32 64 55 61-07 50-91 60-73 60-67 50-39 50-23 50-06 49-89 49-72 55 56 62-00 61-83 61-65 51-49 51-31 51-14 60-97 50-79 50-62 66 67 52-93 62-76 62-58 52-41 62-22 62-06 61-88 61-70 51-63 67 53 53-86 63-68 63-60 53-32 63-14 52-97 62-79 62-61 62-43 68 69 64-79 64-61 54-42 64-24 64-06 63-88 63-70 68-61 53-34 69 60 55-72 65-53 56-34 56-16 64-97 54-79 64-61 64-42 64-24 60 61 66-65 56-46 56-26 66-08 56-89 66-70 55-52 66-33 55-14 61 62 67-58 57-38 67-19' 57-00 66-80 56-62 56-43 66-23 66-06 62 63 68-51 68-31 68-11 67-92 67-72 67-53 57-34 57-14 66-96 63 64 59-42 59-23 69-03 68-84 58-64 58-44 68-25 58-06 67-86 64 66 60-36 60-16 69-96 59-76 69-66 69-36 69-16 58-96 58-76 65 66 61-29 61-08 60-87 60-68 60-47 60-27 60-07 59-86 69-66 66 67 62-22 62-01 61-79 61-60 61-38 61-18 60-98 60-77 60-67 67 63 63-16 62-93 62-72 62-51 62-30 62-10 61-89 61-68 61-47 68 69 64-08 63-86 63-64 63-43 63-22 63-01 62-80 62-68 62-33 69 70 66-00 64-79 64-57 64-36 64-13 63-92 63-71 63-49 63-28 70 71 65-93 65-71 66-49 66-27 65-06 64-33 64-62 64-40 64-18 71 72 66-86 66-64 66-42 60-19 65-96 65 76 65-53 65-30 66-09 72 73 67-79 67-57 67 34 67-11 66-88 66-66 66-44 66-21 66-99 73 74 68-61 68-49 68-26 68-03 67-80 67-67 67-36 67-12 66-90 74 75 69-64 69-42 69-18 68-95 68-71 68-49 68-26 68-03 67-80 75 76 70-57 70-34 70-10 69-87 69-03 69-40 69-17 68-93 63-70 76 77 71-50 71-27 71-03 70-79 70-54 70-31 70-08 09-84 69-61 77 78 72-43 72-19 71-96 71-70 71-46 71-22 70-99 70-75 70-51 78 79 73-36 73-12 72-87 72-62 72-88 72-14 71-90 71-65 71-42 79 80 74-29 74-04 73-79 73-54 73-30 73-06 72-81 72-66 72-32 80 81 76-22 74-97 74-71 74-46 74-22 73-96 73-72 73-47 73-22 81 82 76-16 75-89 76-63 75-38 76-13 74-83 74-63 74-37 74-13 82 83 77-08 76-82 76-56 76-30 76-06 76-79 76-54 76-23 75-03 83 84 78-00 77-74 77-48 77-22 76-96 76-70 76-45 76-19 76-94 84 85 78-93 73-67 78-40 78-14 77-88 77-02 77-36 77-10 76-34 35 86 79-86 79-69 79-32 79-06 78-30 73-63 73-27 78-00 77-74 86 87 80-79 80-62 80-25 79-98 79-71 79-44 79-18 78-91 78-66 87 88 81-72 81-44 81-17 80-90 80-63 80-36 80-09 79-82 79-65 38 89 82-65 32-37 82-09 81-82 81-65 31-27 81-00 80-72 80-46 89 90 83-67 83-30 83-02 82-74 82-46 82-18 81-91 81-63 81-36 90 91 84-50 34-22 83-94 33-66 83-38 33-09 82-82 82-64 82-26 91 92 86-43 86-16 84-86 84-63 84-29 84-01 83-78 83-44 83-17 92 93 86-36 86-08 86-79 86-50 36-21 84-92 84-64 84-36 84-07 93 94 87-28 87-00 86-71 86-42 86-13 86-83 85-65 85-26 34-98 94 95 88-21 87-93 87-63 87-34 87-04 86-75 86-46 86-17 85-88 9c 96 89-14 88-85 88-55 83-26 87-96 , 87-66 87-37 87-07 86-78 96 97 90-07 89-78 89-48 89-18 88-87 88-57 88-28 87-98 87-69 97 98 91-00 90-70 90-40 90-09 39-79 89-48 39-19 88-89 88-59 98 99 91-93 91-63 91-32 91-01 90-71 90-40 90-10 89-79 89-50 99 100 02-86 92-56 92-24 91-93 91-02 91-31 91-01 90-70 90-40 100 TABLE 20— Continued. II. Table for reducing the Deduct from the barometric pressure 1 mm. for temperature between 0" and 12" for the expansion 760 no 712 714 716 718 720 722 724 7-26 728 760 1 0-934 0-937 0-940 0-942 0-945 0-947 0-950 0-953 0-955 0-958 1 2 1-868 1-874 1-879 1-884 1-890 1-895 1-900 1-905 1-911 1-916 2 3 2-803 2-810 2-818 2-826 2-834 2-842 2-850 2-858 2-866 2-874 3 4 3-738 3-747 3-758 3-768 3-779 3-789 3-800 3-810 3-821 3-832 4 6 4-672 4-685 4-697 4-711 4-724 4-736 4-750 4-763 4-777 4-790 5 6 5-607 6-621 6-637 5-663 5-669 6-684 6-700 5-716 5-732 5-747 6 7 6-640 6-568 6-677 6-696 6-614 6-681 6-650 6-668 6-687 6-706 7 8 7-474 7-494 7-616 7-637 7-668 7-678 7-600 7-621 7-642 7-663 8 9 8-409 8-431 8-456 8-479 8-503 8-626 8-650 8-673 8-698 8-621 9 10 9-34 9-37 9-40 9-42 9-45 9-47 9-50 9-63 9-65 9-68 10 11 10-28 10-81 10-34 10-86 10-39 10-42 10-45 10-48 10-61 10-54 11 12 11-21 11-24 11-27 11-30 11-34 11-37 11-40 11-43 11-46 11-60 12 13 12-14 12-18 12-21 12-24 12-28 12-31 12-35 12-38 12-41 12-46 13 14 13-08 13-12 13-16 13-19 13-23 13-26 13-80 13-34 13-37 13-41 14 IS 14-02 14-06 14-10 14-13 14-17 14-21 14-25 14-29 14-33 14-37 15 16 14-95 14-99 16-03 16-07 16-11 16-15 15-20 16-24 16-28 15-33 16 17 16-88 15-93 16-98 16-02 16-06 16-10 16-15 16-19 16-23 16-28 17 18 16-82 16-87 16-92 16-96 17-01 17-06 17-10 17-16 17-19 17-24 18 19 17-76 17-81 17-86 17-90 17-95 18-00 18-06 18-10 18-16 18-21 19 20 18-68 18-74 18-79 18-84 18-90 18-96 19-00 19-05 19-11 19-16 20 21 19-62 19-68 19-73 19-78 19-84 19-90 19-95 20-00 20-06 20-12 21 22 20-66 20-61 20-67 20-72 20-78 20-84 20-90 20-96 21-01 21-07 22 23 21-49 21-65 21-61 21-66 21-73 21-79 21-86 21-91 21-97 22-03 23 24 22-43 22-49 22-56 22-61 22-68 22-74 22-80 22-86 22-92 22-99 24 25 23-36 23-42 23-49 23-56 23-62 23-69 23-75 23-81 23-88 23-95 25 26 24-29 24-36 24-43 24-50 24-67 24-64 24-70 24-77 24-83 24-90 26 27 25-23 26-30 25-37 25-44 25-51 26-68 25-66 25-72 25-79 26-86 27 28 26-16 26-23 26-30 26-37 26-45 26-63 26-60 26-67 26-74 26-82 28 29 27-10 27-17 27-24 27-31 27-40 27-48 27-56 27-62 27-70 27-78 29 30 28-03 28-10 28-18 28-26 28-34 28-42 28-60 28-68 28-66 28-74 30 31 28-97 29-04 29-12 29-20 29-29 29-37 29-45 29-63 29-62 29-70 31 32 20-90 29-98 30-06 30-14 30-23 30-32 30-40 30-48 30-57 30-66 32 33 30-83 30-91 31-00 31-08 31-17 31-26 31-35 31-43 31-62 31-61 33 34 31-77 81-86 31-94 32-03 32-12 82-21 32-30 32-39 32-48 32-67 34 86 32-71 32-79 32-88 32-97 33-07 33-16 33-26 33-34 aaii 33-63 85 36 33-64 38-73 33-82 33-91 34-01 34-10 34-20 34-29 84-39 34-49 36 37 34-67 34-66 34-76 34-86 34-96 85-05 36-16 35-25 85-35 35-45 37 38 36-60 35-60 36-70 35-80 85-90 86-00 36-10 36-20 36-30 36-40 SS 39 36-44 86-54 S6-64 36-74 36-85 36-95 37-05 37-15 37-26 37-37 39 10 37-38 37-48 37-68 37-68 37-79 37-89 SS-00 38-10 38-21 38-32 40 41 38-31 38-41 38-52 38-62 38-74 38-84 38-95 39-05 39-17 39-28 41 42 39-23 39-35 39-46 39-67 39-69 39-79 39-90 40-01 40-12 40-23 42 43 40-13 40-29 40-40 40-61 40-62 40-73 40-85 40-96 41-08 41-19 43 44 41-11 41-22 41-34 41-44 41-66 41-68 41-80 41-91 42-03 42-16 44 45 42-06 42-16 42-28 42-89 42-62 42-63 42-75 42-87 42-99 43-11 45 46 42-98 43-10 43-22 43-34 43-46 43-68 43-70 43-82 43-94 44-06 46 47 43-91 44-03 44-15 44-27 44-40 44-52 44-66 44-77 44-90 46-03 47 48 44-84 44-96 45-09 45-22 45-35 46-47 45-60 45-72 46-85 45-98 46-94 47-90 48 49 60 49 45-78 45-91 46-04 46-17 46-30 46-42 46-66 46-67 46-80 60 46-72 46S5 461)7 «7-ll 47-24 47-36 47-60 47-63 47-77 volumes of gases to a pressure of 760 mm. C, and 2 mm. between 13° and 19' C, 3 mm. between S of mercury. " and 25'' 0., to compensate 760 710 712 714 716 718 720 722 721 726 728 760 61 47-66 47-79 47-02 48-06 48-18 48-31 48-46 48-59 48-73 48-86 61 62 48-68 48-72 48-86 48-99 49-13 49-26 49-40 49-64 49-68 49-82 62 63 49-62 49-06 49-79 49-03 50-07 60-21 60-35 60-48 50-64 50-78 63 64 60-46 60-59 50-73 60-87 61-01 61-16 51-30 61-44 61-69 51-73 64 65 51-88 51-63 51-67 61-82 61-96 52-10 62-26 52-39 62-64 52-69 65 66 62-32 62-47 52-61 62-76 62-91 68-05 63-20 63-35 63-60 53-65 66 67 53-26 63-41 63-56 53-70 63-86 54-00 64-15 64-30 64-45 54-60 57 68 54-19 54-34 54-49 54-64 54-79 54-94 66-10 56-25 55-41 65-66 68 59 65-13 66-28 55-43 65-59 65-74 66-89 66-06 66-21 56-37 66-52 69 60 66-07 66-22 66-87 56-63 66-69 66-84 67-00 67-16 67-32 67-47 60 61 67-00 57-15 57-31 57-47 67-63 67-79 67-96 68-11 68-27 58-43 61 62 67-93 58-09 68-26 58-41 68-68 68-74 68-90 69-06 69-23 69-39 62 63 68-87 69-03 69-19 69-36 69-62 69-68 69-85 60-01 60-18 60-35 63 64 69-80 69-96 60-13 60-80 60-47 60-63 60-80 60-97 61-14 61-30 64 65 60-74 60-90 61-07 61-24 61-41 61-68 61-76 61-92 62-09 62-26 66 66 61-67 61-84 62-01 62-18 62-36 62-52 62-70 62-87 63-05 63-22 66 67 62-60 62-77 62-95 63-12 63-30 63-47 63-65 63-82 64-00 64-18 67 68 63-64 63-71 63-89 64-06 64-24 64-42 64-60 64-78 64-96 66-18 68 69 64-47 64-65 64-83 66-01 66-19 65-37 66-65 66-73 66-91 66-09 69 70 66-40 65-58 66-77 66-95 66-14 66-32 66-60 66-68 66-87 67-05 70 71 66-34 66-62 66-71 66-89 67-08 67-26 67-46 67-68 67-82 68-01 71 72 67-27 67-46 67-65 67-83 68-02 68-21 68-40 68-59 68-78 68-97 72 7S 68-20 68-39 68-68 68-77 68-97 69-16 69-35 69-64 69-73 69-92 73 74 69-14 69-33 69-63 69-72 69-92 70-11 70-SO 70-49 70-69 70-88 74 76 7007 70-27 70-47 70-66 70-86 71-06 71-26 71-44 71-64 71-84 76 76 71-01 71-21 71-41 71-60 71-80 72-00 72-20 72-40 72-60 72-80 76 77 71-94 72-14 72-34 72-54 72-76 72-95 73-16 78-35 73-65 73-76 77 78 72-87 7307 73-28 73-48 73-69 73-89 74-10 74-30 74-51 74-71 78 79 73-80 74-01 74-22- 74-42 74-63 74-84 75-06 76-26 76-46 76-67 79 80 74-74 74-94 76-16 76-37 76-68 75-78 76-00 76-21 76-42 76-68 80 81 75-67 76-88 76-10 76-31 76-63 76-74 76-95 77-16 77-37 77-58 81 82 76-60 76-82 77-04 77-26 77-47 77-68 77-90 78-11 78-33 78-64 82 83 77-64 77-76 77-98 78-19 78-41 78-68 78-85 79-07 79-28 79-60 83 84 78-47 78-69 78-91 79-13 79-36 79-67 79-80 80-02 80-24 80-46 84 85 79-41 79-63 79-86 80-08 80-81 80-53 80-76 80-97 81-19 81-41 86 86 80-34 80-67 80-80 81-02 81-26 81-47 81-70 81-92 82-15 82-37 86 87 81-28 81-60 81-74 81-96 82-19 82-42 82-66 82-87 83-10 83-33 87 - 88 82-21 82-44 82-68 82-90 83-13 83-36 83-60 88'88 84-06 84-29 88 89 83-16 83-33 83-62 83-86 84-08 84-31 84-66 84-78 86-02 85-25 89 90 84-09 84-31 84-66 84-79 85 03 86-26 86-60 86-73 86-98 86-21 90 91 85-02 85-26 86-50 86-73 86-98 86-21 86-45 86-69 86-93 87-17 91 92 86-95 86-19 86-44 86-68 86-92 87-16 87-40 87-64 87-89 88-18 92 93 86-89 87-12 87-38 87-62 87-87 88-11 88-86 88-69 88-84 89-08 93 94 87-82 88-06 88-32 88-66 88-81 89-05 89-30 89-64 89-80 90-04 94 96 88-76 89-01 89-26 89-50 89-76 90-00 90-26 90-60 90-76 91-00 95 96 89-69 89-94 90-20 90-45 90-70 90-95 91-20 91-45 91-70 91-95 96 97 90-62 90-87 91-13 91-38 91-64 91-89 92-15 92-40 92-66 92-91 97 98 91-66 91-82 92-07 92-33 92-69 92-84 83-10 93-35 93-62 93-87 98 99 92-49 92-75 93-01 98-26 93-63 93-79 94-06 94-31 94-67 94-83 99 100 93-42 93-68 93-95 94-21 94-47 94-74 06-00 96-26 95-53 96-79 100 44 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 2Q— Continued. II. Table for reducing the 760 730 732 734 736 788 740 742 744 746 748 760 1 0-961 0-963 0-966 0-968 0-971 0-974 0-976 0-979 0-982 0-984 1 2 1-921 1-926 1-932 1-987 1-942 1-947 1-963 1-968 1-963 1-968 2 S 2-882 2-889 2-898 2-905 2-918 2-921 2-929 2-937 2-945 2-953 3 4 3-S42 3-862 3-864 3-874 3-884 3-896 3-906 3-916 3-926 3-987 4 5 4-803 4-816 4-830 4-842 4-865 4-868 4-882 4-896 4-908 4-921 6 6 5-763 6-779 5-796 6-810 6-826 6-842 6-858 5-874 5-890 5-906 6 7 6-724 6-742 6-762 6-779 6-797 6-816 6-834 6 '853 6-871 6-889 7 8 7-684 7-706 7-728 7-747 7-768 7-790 7-810 7-832 7-853 7-874 8 9 8-645 8-668 8-693 8-716 8-739 8-763 8-787 8-811 8-834 8-868 9 10 9-61 9-63. 9-66 9-68 9-71 9-74 9-76 9-79 9-82 9-84 10 11 10-57 10-59 10-62 10-65 10-68 10-71 10-74 10-77 10-80 10-82 11 12 11-63 11-66 11-59 11-62 11-65 11-68 11-71 11-76 11-78 11-81 12 IS 12-49 12-62 12-65 12-69 12-62 12-66 12-69 12-73 12-76 12-79 13 14 13-45 13-48 18-52 13-66 13-59 18-63 13-66 13-70 13-74 13-78 14 15 14-41 14-44 14-48 14-52 14-56 14-60 14-64 14-69 14-73 14-77 15 16 15-87 16-41 16-45 16-49 15-53 15-68 15-62 15-67 16-71 16-76 16 17 16-33 16-37 16-41 16-46 16-60 16-66 16-60 16-65 16-69 16-73 17 18 17-29 17-33 17-38 17-43 17-47 17-62 17-57 17-62 17-67 17-72 18 19 18-26 18-29 18-36 18-40 18-45 18-60 18-56 18-60 18-65 18-70 19 20 19-21 19-26 19-32 19-37 19-42 19-47 19-63 19-63 19-63 19-68 20 21 20-17 20-22 20-28 20-34 20-39 20-44 20-60 20-66 20-61 20-66 21 22 21-13 21-19 21-26 21-31 21-36 21-42 21-48 21-64 21-59 21-66 22 23 22-09 22-16 22-21 22-27 22-88 22-39 22-46 22-6] 22-57 22-64 23 24 23-05 23-11 23-18 28-24 23-30 23-36 23-43 23-60 28-56 23-63 24 25 24-01 24-07 24-14 24-21 24-27 24-34 24-41 24-48 24-64 24-61 25 26 24-97 26-04 26-11 25-18 26-24 26-31 26-38 26-46 26-62 26-69 26 27 25-93 26-00 26-07 26-14 26-21 26-28 26-36 26-43 26-60 26-58 27 28 26-89 26-96 27-04 27-12 27-18 27-26 27-83 27-41 27-48 27-66 28 29 27-85 27-92 28-00 28-08 28-15 28-23 28-81 28-39 28-47 28-65 29 80 28-82 28-89 28-97 29-06 29-18 29-21 29-29 29-37 29-46 29-53 30 81 29-78 29-86 29-94 80-02 80-10 30-18 80-26 30-35 30-48 30-51 31 82 30-74 30-82 30.-91 30-99 81-07 81-16 31-24 31-33 31-41 31-60 32 33 31-70 31-78 31-87 31-96 82-04 82-13 32-21 32-30 32-39 32-48 33 34 82-66 32-76 32-84 82-98 83-01 88-10 33-19 33-28 33-37 33-46 34 85 33-62 33-71 83-80 83-89 33-98 34-07 34-17 34-27 34-36 34-45 36 36 84-58 34-67 34-77 34-86 84-95 36-06 36-16 35-25 36-34 36-43 36 37 35-64 86-63 36-73 36-83 86-92 86-02 86-12 36-22 36-32 36-42 37 38 86-80 86-60 36-70 86-80 36-90 87-00 37-10 37-20 37-80 87-40 38 39 87-47 87-67 87-67 37-77 37-87 37-97 38-07 38-18 38-28 38-39 39 40 88-42 88-52 38-64 88-74 38-84 88-95 39-05 39-16 89-26 89-37 40 41 39-88 39-48 39-60 39-71 39-81 89-92 40-02 40-14 40-24 40-36 41 42 40-84 40-44 40-56 40-68 40-78 40-89 41-00 41-12 41-22 41-34 42 43 41-80 41-4] 41-63 41-64 41-76 41-86 41-97 42-10 42-20 42-32 43 44 42-27 42-38 42-60 42-62 42-73 42-84 42-95 43-07 43-18 48-30 44 46 43-22 48-84 48-46 43-68 43-69 48-81 43-98 44-06 44-17 44-29 45 46 44-18 44-30 44-42 44-64 14-66 44-78 44-90 46-08 45-15 46-27 46 47 45-16 45-26 46-39 45-52 46-64 46-76 45-88 46-01 46-18 46-26 47 48 46-10 46-23 46-86 46-49 46-61 46-73 46-86 46-99 47-12 47-24 43 49 47-06 47-19 47-82 47-44 47-67 47-70 47-83 47-97 48-10 48-23 49 6C 48-03 48-16 48-30 48-42 48-66 48-68 48-82 48-95 49-08 49-21 60 1 REDUCTION OF THE VOLUME OF GASES 45 volumes of gases to a pressure of 760 mm. — Contimud. 760 780 732 734 736 738 740 742 744 746 748 760 61 48-99 49-12 49-26 49-89 49-62 49-65 49-79 49-93 60-06 60-19 61 52 49-96 50-08 60-22 50-36 60-49 60-68 60-77 50-91 61-04 51-18 62 68 60-91 51-05 61-19 61-83 61-46 51-60 61-75 61-89 62-02 52-16 63 64 61-87 52-01 62-16 52-30 62-44 52-68 62-72 52-87 53-01 63-16 64 65 62-88 62-98 63-18 53-27 68-41 58-65 63-70 53-85 68-99 64-14 65 66 63-79 63-94 54-09 64-28 54-87 64-62 64-68 64-83 54-97 65-11 56 67 64-75 54-90 66-06 65-20 66-35 65-50 65-65 66-80 66-96 66-10 67 6S 55-71 65-86 66-02 56-17 66-82 66-47 66-63 66-78 66-98 67-08 68 69 56-67 66-83 66-99 67-14 57-29 67-44 67-60 67-76 67-92 68-07 69 60 67-63 67-79 67-95 58-10 58-26 68-42 68-68 68-74 58-90 69-05 60 61 58-69 58-75 68-91 69-07 69-23 69-89 69-66 69-72 59-88 60-04 61 62 59-65 59-72 69-88 60-04 60-20 60-86 60-53 60-70 60-86 61-02 62 63 60-51 60-68 60-86 61-01 61-17 61-34 61-51 61-68 61-84 62-00 68 64 61-47 61-64 61-81 61-98 62-16 62-82 62-49 62-66 62-82 62-99 64 65 62-43 62-60 62-77 62-94 68-11 63-28 63-46 63-64 68-81 68-98 66 66 63-39 63-67 63-74 63-91 64-08 64-26 64-44 64-62 64-79 64-96 66 67 64-35 64-53 64-71 64-88 66-06 66-23 65-41 66-69 65-77 65-94 67 68 65-31 66-50 65-68 05-85 66-02 66-20 66-38 66-56 66-74 66-92 68 69 66-27 66-46 66-64 66-82 67-00 67-18 67-37 67-56 67-73 67-91 69 70 67-24 67-42 67-61 67-79 67-97 68-16 68-34 68-63 68-71 68-89 70 71 68-20 68-39 68-58 68-76 68-94 69-13 69-82 69-51 69-69 69-88 71 72 69-16 69-36 69-64 69-78 69-92 70-11 70-30 70-49 70-68 70-86 72 73 70-12 70-31 70-61 70-69 70-88 71-08 71-27 71-47 71-66 71-85 78 74 71-08 71-28 71-48 71-66 71-85 72-06 72-25 72-46 72-64 72-83 74 75 72-04 72-24 72-44 72-68 72-82 78-02 73-22 73-42 73-62 73-82 76 76 73-00 73-20 78-40 73-60 73-80 74-00 74-20 74-40 74-60 74-80 76 77 78-96 74-17 74-37 74-57 74-77 74-97 76-18 76-39 75-69 75-79 77 78 74-98 76-12 76-33 75-63 75-74 76-96 76-16 76-37 76-67 76-77 78 79 76-88 76-09 76-80 76-60 76-71 76-92 77-13 77-34 77-65 77-76 79 80 76-84 77-05 77-27 77-47 77-68 77-90 78-10 78-82 78-53 78-74 80 81 77-80 78-02 78-28 78-44 78-66 78-87 79-08 79-30 79-51 79-72 81 82 78-76 78-98 79-20 79-41 79-62 79-84 80-06 80-28 80-60 80-71 82 83 79-72 79-94 . 80-16 80-88 80-60 80-82 81-04 81-26 81-48 81-69 83 84 80-68 80-90 81-12 81-84 81-66 81-79 82-01 82-24 82-46 82-68 84 86 81-64 81-87 82-10 82-81 82-63 82-76 82-90 88-22 83-44 83-66 85 86 82-60 82-83 88-06 83-28 83-60 83-73 88-97 84-20 84-42 84-64 86 87 83-66 83-79 84-02 84-26 84-48 84-71 84-94 86-17 85-40 85-62 87 88 84-52 84-76 86-00 85-22 85-46 85-68 85-92 86-16 86-38 86-61 88 89 86-48 86-72 85-08 86-19 86-42 86-66 80-S9 87-18 87-36 87-69 89 90 86-45 86-68 86-98 87-16 87-39 87-63 87-87 88-11 88-34 88-68 90 91 87-41 87-65 87-89 88-12 88-36 88-61 88-86 89-09 89-88 89-56 91 92 88-37 88-61 88-86 89-09 89-33 89-68 89-82 00-07 90-31 90-66 92 93 89-33 89-57 89-82 90-06 90-30 90-56 90-80 91-05 91-29 91-68 93 94 90-29 90-54 90-79 91-03 91-27 91-53 91-78 92-03 92-27 92-61 94 95 91-25 91-50 91-76 92-00 92-26 92-60 92-76 93-00 93-25 93-50 95 96 92-21 92-46 92-72 92-97 98-22 93-47 93-78 93-98 94-28 94-48 96 97 98-17 93-43 93-68 93-98 94-19 94-45 94-71 94-96 95-22 96-47 97 98 94-13 94-39 94-66 94-90 95-16 95-42 05-68 96-94 96-20 96-45 98 99 95-09 96-35 96-61 96-87 96-13 96-39 96-66 96-92 97-18 97-43 99 100 96-06 96-82 96-58 96-84 97-11 97-37 97-63 97-89 98-16 98-42 100 46 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 20— Continued. II. Table for reducing the 760 760 762 754 756 768 762 764 766 768 770 760 1 0-9S7 0-989 0-092 0-996 0-997 1-003 1-605 1-098 1-011 1-013 1 2 1-974 1-979 1-984 1-989 1-995 2-906 2-011 2-016 2-821 2-826 2 3 2-9i0 2-968 2-976 2-984 2-992 3-8*7 3016 3-024 3-832 3-039 3 4 3-947 ,3-958 8-968 3-979 3-990 4-010 4-021 4-032 4-042 4-852 4 S 4-934 4-947 4-960 4-974 4-987 6-013 5-026 5-040 6-063 5-066 5 6 6-921 5 -937 5-952 6-968 6-984 6-016 6-082 6-047 6-063 6-079 6 V S'908 6-92S 6-944 6-963 6-982 7-018 7-037 7-055 7-974 7-092 7 8 7-894 7-916 7-936 7-968 7-979 8-021 8-942 8-063 8-984 8-106 8 9 8-SSl 8-995 8-929 8-952 8-977 9-023 9-04S 9-071 9-896 9-110 9 10 9-87 9-89 9-92 9-96 9-97 10-03 10-05 10-08 10-11 10-13 10 11 10-85 10-88 10-91 10-94 10-97 11-03 11-06 11-09 11-12 11-14 11 12 11-84 11-87 11-9(1 11-94 11-97 12-04 12-07 12-10 12-13 12-16 12 13 12-83 12-86 12-89 12-93 12-96 13-04 18-07 13-10 18-14 13-17 13 14 13-82 13-86 13-18 13-92 13-96 14-04 14-07 14-11 14-15 14-17 14 15 14-81 14-84 14-87 14-92 14-96 16-04 15-08 15-12 15-16 15-19 15 16 15-79 15-83 15-87 16-91 15-95 16-05 16-89 16-13 16-17 16-21 16 17 16-78 l«-«2 16-S6 16-91 16-95 17-85 17-99 17-14 17-18 17-22 17 18 17-77 17-81 17-85 17-90 17-95 18-66 18-10 18-16 18-19 18-28 18 19 18-75 18-8» 18-86 18-98 18-95 19-05 19-10 19-16 19-20 19-26 19 20 19-74 19-79 19-84 19-89 19-95 20-06 20-11 29-16 20-21 20-26 20 21 20-72 29-77 20-83 20-89 20-94 21-05 21-11 21-17 21-22 21-27 21 22 21-71 21-76 21 -S2 21-88 21-94 22-95 22-12 22-18 22-23 22-28 22 23 22-70 22-75 22-81 22-88 22-94 23-06 23-12 23-18 23-24 23-38 23 24 23-69 23-74 23-80 23-87 23-93 24-06 24-13 24-19 24-25 24-31 24 25 24-67 24-73 24-SO 24-87 24-93 25-06 25-13 25-20 25-26 25-32 25 26 25-66 26-72 25-79 25-86 25-93 26-06 26-14 26-21 26-27 26-34 26 27 26-66 26-71 26-78 26-86 28-93 27-07 27-16 27-22 27-28 27-36 27 28 27-63 27-70 27-77 27-S6 27-92 28-97 28-15 28-23 28-20 28-36 28 29 28-62 28-69 28-76 28-84 28-92 29-97 29-16 29-24 29-30 29-87 29 80 29-60 29-68 29-7S 29-84 29-92 30-07 30-16 30-24 30-32 30-39 80 SI 30-69 30-67 39-75 30-84 30-92 31-08 31-17 31-26 31-33 81-41 31 82 31-68 31-66 31-74 31-83 31-92 32-08 32-17 82-26 32-34 82-42 82 33 32-66 - 32-65 32-73 32-82 82-91 83-98 33-18 83-27 33-36 38-43 33 84 33-66 33-64 83-73 33-82 33-91 34-09 84-18 84-28 34-36 34-45 34 3S 34-54 34-63 34-72 34-82 34-91 35-09 35-19 36-28 36-37 36-46 35 86 36-62 35-62 35-71 36-81 36-91 36-09 36-19 36-29 86-88 36-47 36 87 36-51 36-61 36-71 36-81 36'9« 37-09 37-20 37-30 37-39 37-49 37 38 37-60 87-60 37-70 87-80 87-90 38-10 38-20 38-30 38-40 38-60 88 89 38-49 38-59 38-69 35 -8» 38-90 39-10 39-21 39-31 39-41 39-61 39 40 39-47 89-68 39-68 39-79 39-90 40-10 40-21 40-32 40-42 40-52 40 41 40-46 40-66 40-67 40-79 40-89 41-11 41-22 41-38 41-43 41-64 41 42 41-44 41-56 41-66 41-78 41-89 4211 42-22 42-34 42-44 42-65 42 43 42-43 42-54 42-66 42-78 42-89 48-11 43-23 43-35 43-46 43-56 43 44 43-42 43-53 43-65 43-77 43-89 44-12 44-28 44-35 44-46 44-58 44 45 44-40 44-62 44-64 44-76 44-88 45-12 46-24 45-36 45-47 45-69 45 46 45-39 45-51 45-63 45-76 45-88 46-12 46-24 46-86 46-48 46-60 46 47 46-88 46-60 46-63 46-76 46-88 47-12 47-25 47-38 47-49 47-61 47 48 47-36 47-49 47-62 47-76 47-87 48-18 48-26 48-39 48-61 48-63 48 49 48-36 48-48 48-61 48-74 48-87 49-13 49-26 49-40 49-52 49-64 49 50 49-34 49-47 49-60 49-74 49-87 50-13 60-26 60-40 50-53 50-66 60 REDUCTION OF THE VOLUME OF GASES 47 volumes of gases to a pressure of 760 mm. — Continued. 760 750 762 754 756 758 762 764 786 788 770 760 61 60-33 60-46 60-60 60-74 60-87 61-14 61-27 51-41 61-54 61-67 61 52 61-32 51-45 51-69 61-73 61-87 62-14 62-28 62-42 62-66 52-68 62 53 52-30 52-44 62-68 52-78 62-87 63-14 63-28 53-42 63-56 63-70 63 54 53-29 63-43 63-67 63-72 53-86 64-14 64-28 54-48 64-67 64-72 64 55 64-28 64-42 64-56 64-71 54-86 65-15 65-29 55-44 66-68 65-73 65 56 65-26 55-41 56-56 55-71 56-86 56-16 66-29 68-45 66-69 66-74 56 67 56-26 56-40 66-56 66-70 68-86 67-15 57-30 67-45 67-60 67-76 67 68 67-24 67-39 67-64 67-69 67-85 58-16 68-80 58-46 58-61 68-77 63 69 58-22 58-38 58-53 68-69 68-85 59-16 69-31 69-47 59-62 69-78 59 60 59-21 69-S7 59-62 69-68 59-84 60-16 80-32 60-47 80-83 60-79 60 61 60-20 60-36 60-52 60-68 60-84 61-16 61-32 81-48 61-64 81-81 61 62 61-19 61-35 61-61 61-67 61-84 62-16 62-33 62-49 82-86 62-82 62 63 62-17 62-34 62-60 62-67 62-83 68-17 63-38 68-50 63-67 63-84 63 64 63-16 63-33 63-49 63-68 63-83 84-17 64-34 64-51 64-68 64-85 64 65 64-16 64-32 64 49 64-66 64-83 66-17 85-34 65-61 66-69 65-86 65 66 65-13 66-31 86-43 86-65 65-82 68-17 86-35 66-52 66-70 66-88 66 67 66-12 66-30 66-47 66-64 68-82 67-18 67-36 87-53 87-71 67-89 87 63 67-10 67-29 67-46 67-64 67-82 68-18 68-36 68-64 68-72 68-90 63 69 68-09 68-28 68-45 68-63 68-82 69-18 69-38 69-54 89-73 69-91 89 70 69-08 69-26 69-44 69-63 69-82 70-18 70-37 70-65 70-74 70-92 70 71 70-07 70-25 70-43 70-62 70-81 71-19 71-87 71-56 71-75 71-94 71 72 71-05 71-24 71-43 71-62 71-81 72-19 72-38 72-67 72-76 72-96 72 73 72-04 72-23 72-42 72-81 72-81 73-19 73-38 73-67 73-77 73-97 73 74 73-03 73-22 73-41 73-61 73-80 74-19 74-39 74-68 74-78 74-98 74 76 74-01 74-21 74-40 74-60 74-80 75-20 76-39 76-69 75-79 76-99 75 76 75-00 75-20 76-40 75-60 75-80 76-20 78-40 78-60 76-80 77-01 76 77 75-99 76-19 76-39 76-59 76-79 77-20 77-40 77-60 77-81 78-02 77 78 76-97 77-18 77-38 77-58 77-79 78-20 78-41 78-61 78-82 79-03 78 79 77-96 78-17 78-37 78-58 78-79 79-21 79-41 79-82 79-83 80-04 79 80 78-94 79-16 79-36 79-68 79-79 80-21 80:42 80-63 80-84 81-08 80 81 79-93 80-15 80-35 80-67 80-79 81-21 81-42 81-64 81-86 82-07 81 82 80-92 81-14 81-36 81-56 81-78 82-21 82-43 82-66 82-87 88-09 82 83 81-91 82-13 82-34 82-66 82-78- 83-22 83-44 83-66 83-88 84-10 83 84 82-90 83-12 83-34 83-58 83-78 84-22 84-44 84-66 84-89 86-11 84 85 83-88 84-11 84-33 84-55 84-78 85-22 85-46 86-67 85-90 86-13 85 86 84-87 86-10 85-82 35-55 85-78 86-22 S6-46 86-67 86-91 87-14 86 87 86-85 86-08 86-81 88-54 86-77 87-23 87-46 87-68 87-92 88-15 87 88 86-84 87-07 87-80 87-64 87-77 88-23 88-47 88-69 88-93 89-17 88 89 87-82 88-06 88-29 88-63 88-77 89-23 89-47 89-70 89-94 90-18 89 90 88-81 89-05 89-29 89-52 89-77 90-23 90-48 90-71 90-95 91-19 90 91 89-80 90-04 90-28 90-62 90-76 91-24 91-48 91-72 91-98 92-21 91 92 90-79 91-03 91-27 91-61 91-78 92-24 92-49 92-73 02-97 93-22 92 93 91-77 92-02 92-26 92-51 92-76 93-24 93-49 98-74 98-93 94-23 93 94 92-76 93-01 93-26 93-60 93-76 94-24 94-49 94-74 04-99 96-24 94 95 93-74 94-00 94-25 94-60 94-76 96-26 95-50 96-76 96-00 98-26 95 96 94-78 94-98 95-24 95-49 95-75 96-25 96-51 96-78 97-01 97-27 96 97 95-72 95-97 96-28 98-49 98-76 97-25 97-61 97-77 08-02 98-29 97 98 96-70 96-96 97-22 97-48 97-74 98-26 98-52 98-77 9903 99-30 98 99 97-69 97-95 98-21 98-48 08-74 99-26 99-52 99-78 100-04 100-31 99 100 98-68 98-95 99-21 99-47 99-74 100-26 100-53 100-79 101-05 101-32 100 48 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 21.— FACTORS FOR REDUCING A TEMPERATURE 0° Centigrade, and 760 millimetres, or 32° Centigrade. 00. 1-1. 2-2. 3-3. 4-4. 6-6. 6-7. 7-8. 8-9. Fahrenheit. 32°. 34". 36". 38°. 40". 42". 44". 46°. 48". In. Milli- metres. 27-5 698-6 -9191 -9154 ■9116 ■9079 ■9043 -9007 ■8972 -8936 -8890 27-6 701-0 -9224 •9188 ■9149 ■9112 ■9076 •9039 -9005 ■8969 -8932 27-7 703-6 -9268 -9221 ■9183 ■9145 ■9109 •9072 ■9037 ■9001 -8964 27-8 706-1 •9291 ■9254 •9216 ■9179 ■9142 •9106 ■9070 ■9034 -8996 27-9 708-6 -9325 •9288 •9249 •9212 ■9174 •9138 ■9102 ■9067 -9029 28-0 ni-2 •9358 -9321 •9282 •9244 ■9208 •9170 •9135 ■9099 -9061 28-1 713-7 -9391 ■9354 •9315 •9278 ■9241 •9203 •9167 ■0131 ■9093 28-2 716-3 -9425 ■9387 •9348 ■9310 ■9273 •9236 ■9200 ■9164 ■9126 28-3 718-8 •9468 ■9421 •9382 ■9344 ■9306 •9289 •9233 ■9197 ■9168 28-4 721-3 -9491 ■9464 •9416 ■9377 -9339 •9801 ■9265 ■9229 ■9190 28-6 723-9 -9526 ■9487 •9448 -9410 -9372 -9334 ■9298 '9262 ■9223 28-6 726-4 •9558 ■9620 •9481 -9443 -9405 •9367 •9331 ■9294 ■9265 28-7 728-9 •9592 ■9654 ■9514 -9476 -9438 •9400 ■9364 ■9327 ■9287 28-8 731-5 •9626 •9687 •9647 ■9509 ■9471 •9432 ■9396 ■9369 ■0320 28-9 734-0 •9669 •9620 ■9680 ■9542 ■9604 -9465 ■9429 ■9392 ■9362 29-0 786-6 •9692 •9654 •9613 ■9676 ■9536 -9498 -9462 ■9424 -9885 29-1 789-1 •9726 •9687 ■9647 •9608 ■9569 •9631 •9494 -9457 -9417 29-2 741-6 •9759 ■9720 ■9680 •9640 ■9602 -9663 ■9527 ■9489 ■9449 29-3 744-2 ■9792 •9763 ■9713 •9674 ■9635 -9696 ■9669 ■9522 •9481 29-4 746-7 -9826 •9787 -9746 •9707 ■9668 -9629 ■9592 ■9654 ■9514 29-6 749-3 •9869 ■9820 ■9779 ■9740 ■9701 •9662 -9624 •9687 ■9546 29-6 751-8 •9893 ■9863 ■9812 ■9773 ■9733 •9694 ■9667 ■9619 ■9578 29-7 754-3 •9926 ■9887 •9846 -9806 ■9766 •9727 ■9690 •9652 •9611 29-8 766-9 -9969 ■9920 •9879 •9839 ■9800 -9760 ■9722 •9684 '9643 29-9 769-4 ■9993 ■9964 ■9912 -9872 ■9832 -9793 ■9755 ■9717 '9676 300 762-0 1-0026 ■9987 ■9946 -9906 ■9866 -9826 ■9788 ■9749 ■9708 80-1 764-5 1-0060 1-0020 ■9978 ■9938 ■9898 -9858 ■9820 ■9782 •9740 30-2 767-0 1-0093 10063 l^OOll ■9971 ■9931 ■9891 ■9853 ■9814 ■9778 30-3 769-6 1-om 1-0086 1-0044 10004 ■9964 '9924 •9885 ■9846 '9805 80-4 772-1 1-0160 1-0120 1-0078 10087 ■9997 •9957 ■9918 ■9879 '9837 80-B 774-7 1^0194 1-0153 1-0111 1-0070 1-0030 ■9989 ■9960 ■9911 ■9870 30-6 777-2 1-0227 1-0186 1-0144 1-0103 1-0063 1-0022 ■9983 ■9944 '9902 80-7 779-7 1-0260 1-0220 1-0177 1-0136 1-0096 10055 1-0016 ■9976 '9935 80-8 782-3 1-0294 1-0253 1-0210 1-0169 10128 1-0087 10048 r0009 ■9967 30-9 784-8 1-0827 1-0286 1-0243 1-0202 1-0164 1-0120 10081 1-0041 10000 31-0 787-4 10360 1-0319 1-0276 1-0236 1-0194 1-0168 1-0114 1-0074 10032 NORMAL TEMPEllATUEE AND PRESSURE 49 GIVEN VOLUME OF GAS TO NORMAL AND PRESSURE. Fahrenheit, and 29 '92 inches barometric pressure. Centigrade. 10-0. 11-1. 12^2. 18-3. 14^4. 16^6. 16-7. ■ 17-8. Fahrenheit. 60-. 62". 54". 56". 68'. 60". 62-. 64°. In. Milli- metres. 27-5 698-6 •8867 ■8832 •8797 •8763 ■8728 •8696 ■8661 -8628 27-6 701-0 -8900 ■8864 •8829 •8795 ■8760 •8726 ■8603 •8660 27-7 703-6 •8932 ■8897 •8861 ;8827 •8792 •8758 •8724 •8691 27-8 706-1 -8964 ■8928 ■8803 •8859 ■8823 •8790 •8766 -8722 27-9 708-6. •8996 ■8960 •8926 •8890 ■8856 •8821 •8787 -8764 28-0 711-2 •9029 •8992 •8957 •8922 ■8887 •8853 •8819 -8785 28-1 713-7 •9060 ■9025 •8989 •8964 •8910 •8884 •8860 -8816 28-2 716-3 ■9093 ■9067 ■9021 •8986 ■8061 •8916 •8882 -8848 28 -S 718-8 •9125 •9089 ■9053 •9018 ■8983 •8948 •8913 -8879 28-4 721-3 •9157 •9121 ■9085 ■9050 ■9014 •8979 •8945 -8011 28-5 723-9 •9189 •9153 ■9117 ■9082 ■9046 •9011 ■8976 -8942 28-6 726-4 -9222 ■9185 ■9149 ■9114 ■9077 •9043 ■ooos -8073 28-7 728-9 -9254 ■9218 ■9181 ■9146 ■9109 ■9074 ■9030 -9005 28-8 731-6 -9286 ■9250 ■9213 ■9177 ■0141 ■9106 ■9071 -9036 28-9 734-0 •9318 ■9282 ■9245 ■9209 ■0173 ■9188 ■9102 -0067 29-0 736-6 •9351 ■9314 ■9277 ■9241 ■9206 ■9169 ■9134 -9009 29-1 739-1 •9383 ■9846 ■9309 ■9278 ■9236 ■9201 ■9165 ■0130 29-2 741-6 •9416 ■9378 ■0341 ■9305 •0268 ■9233 ■9197 ■0162 29-3 744-2 •9448 ■9410 ■9373 ■9336 ■9300 ■9264 ■9S28 ■9198 29 '1 746-7 -9480 ■9443 ■9405 ■0368 ■9332 ■9296 ■9260 ■9224 29-5 749-3 ■9512 ■9475 ■9437 ■9400 ■9363 ■0328 ■9291 ■9266 29-6 761-8 •9544 ■9606 ■9469 ■0432 ■9896 •9359 ■9323 ■9287 29-7 764-8 -9577 ■9539 ■9601 ■9464 ■9427 ■9300 ■9354 ■9318 29-8 756-9 -9609 ■9571 ■9633 ■9406 ■9459 ■9422 ■9386 ■9360 29-9 759-4 -9641 ■9603 ■9666 ■9628 ■9490 ■9454 ■9417 ■9381 80-0 762-0 -9673 ■0636 ■9697 ■9560 ■9622 ■9486 ■9449 ■9413 30-1 764-5 -9706 ■9667 •9629 ■9691 ■9654 ■0617 ■9480 -9444 30-2 767-0 -9738 ■9700 ■9661 ■9623 •9586 ■9649 ■9512 -9475 30-8 769-6 -9770 •9781 ■9693 •9655 •9617 ■0680 ■9643 -9607 30-4 772-1 •9802 ■9764 ■0726 ■9687 ■9640 •9612 •9575 -9638 3«-5 774-7 -9836 ■9796 ■9767 ■9719 ■0681 ■9643 ■9606 -9569 30-6 777-2 •9867 ■9828 ■9789 ■0751 ■9712 ■9675 ■9638 -9601 30-7 779-7 ■9899 •9860 ■9821 ■9782 ■9744 ■9707 ■9669 -9632 30-8 782-3 •9931 •9892 ■9863 ■9816 ■9776 •9738 •9701 -9664 30-9 784-8 •9963 •9924 ■9885 •9846 ■9807 ■9770 •9732 •0696 31-0 787-4 •9996 •9966 •9917 •9878 ■9840 ■9801 ■9764 -9726 50 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 21— Cora«WMed!. Centigrade. 18-9. 20. 21-1. 22-2. 23^3. 24^4. 25-6. 26-7. Fahrenheit. 66'. 68'. 70°. 72". 74-. 76-. 78°. 80°. In. MQU- metres. 27-5 698-5 -8695 •8563 -8630 -8498 •8466 •8435 -8403 ■8372 27-6 701-0 •8626 •8594 ■8661 -8629 •8497 ■8465 -8434 -8403 27-7 703-6 -8658 •8625 •8592 -8560 •8628 -8496 •8464 -8433 27-8 706-1 -8689 •8666 ■8623 ■8691 •8669 -8527 •8496 •8463 27-9 708-6 ■8720 •8687 •8664 •8622 •8589 ■8667 •8526 •8494 28 711-2 ■8751 •8718 •8685 ■8653 •8620 -8588 •8656 •8524 28-1 713-7 -8783 •8760 •8716 ■8684 •8051 ■8619 •8587 •8565 28-2 716-3 ■8814 -8781 •8747 ■8714 •8682 •8649 •8617 •8586 28-3 718-8 •8845 -8812 •8778 ■8745 •8713 ■8680 •8648 •8616 28-4 721-8 •8876 -8843 •8809 •8776 •8743 ■8711 •8678 •8646 28-6 723-9 ■8908 -8874 ■8840 •8807 •8774 ■8741 •8709 ■8677 28-6 726-4 -8939 •8905 ■8872 -8838 -8805 -8772 •8739 ■8707 28-7 728-9 ■8970 •8986 ■8903 •8869 -8836 ■8803 •8770 ■8738 28-8 731-5 •9002 •8968 •8934 •8900 -8366 -8833 •8800 ■8768 28-9 734-0 ■9033 •8999 •8965 •8931 -8897 ■8864 •8831 ■8798 290 736-6 -9064 •9030 ■8996 -8962 -8928 -8895 •8862 ■8829 29-1 739-1 -9095 •9061 ■9027 -8993 -8969 -8925 -8892 ■8869 29-2 741-6 -9127 •0092 ■0068 -9023 -8990 -8956 •8923 ■8890 29-3 744-2 -9158 ■9123 ■9089 •9064 •9020 -8987 •8963 •8920 29-4 746-7 -9189 ■9154 ■9120 •9085 •9051 ■9017 •8984 •8951 29-6 749 -S -9220 ■9186 ■9161 •9116 -9082 ■9043 ■9014 •8981 29-6 751-8 -9252 -9217 •9182 •9147 •9113 ■0079 ■9046 •9012 29-7 764-3 -9283 -9248 ■9213 •9178 -9144 ■9109 ■9076 -9042 29-8 766-9 -9314 ' ■9279 ■9244 •9209 -9174 ■9140 ■9106 -9072 29 9 759-4 •9345 ■9310 ■9275 •9240 -9205 ■9171 •9137 -9103 800 762-0 ■9377 ■9341 ■9306 •9271 -9286 ■9201 ■9167 •9133 301 764-5 ■9408 -9372 ■9337 •9302 -9267 ■9232 ■9198 •9164 30-2 767-0 -9489 -9403 ■9368 •9338 •9297 •9263 ■9228 •9194 30-3 769-6 -9470 -9435 ■9329 •9363 -9328 •9293 ■9259 •9225 30-4 772-1 -9502 -0466 -9430 •9394 •9359 •9324 ■9289 •9256 30-5 774-7 -9533 ■9497 •9461 •9425 -9390 •9365 ■9320 •9286 30-6 777-2 •9664 ■9528 ■9492 •9466 •9421 -9385 ■9351 '9316 80-7 779-7 -9695 ■9559 -9623 •9487 -0461 •9416 ■9381 •9346 30-8 782-3 -9627 ■9590 -9654 •9618 •9482 •9447 •9412 •9377 30-9 784-8 •9658 ■9621 ■9585 •9649 •9613 •9477 •9442 •9407 31-0 787-4 •9689 ■9663 ■9616 •9580 •9544 •9608 •9473 ■9438 WATEB AT DIFFERENT TEMPERATURES 51 TABLE 21a.— VOLUMES OF WATER AT DIFFER- ENT TEMPERATURES. (Rossetti.) Temp. Temp. Temp. '0. -c. '0. ^ 1 14 1-000566 40 1-007531 1 '999947 15 1-000695 45 1-009541 2 0-999908 16 1-000846 50 1-011766 3 0-999885 17 1-001010 65 1-014100 i 0-999877 18 1-001184 60 1 -016590 6 0-999883 19 1-001370 65 1-019302 6 0-999903 20 1-001567 70 1-022246 7 0-999938 21 1-001776 75 1-025440 8 0-999986 22 1-001995 80 1-028581 9 1 -000048 23 1-002226 85 1-031894 10 1-000124 24 1-002465 90 1-035397 11 1-000213 25 1 -002715 95 1-039094 12 1-000314 30 1-004064 100 1-042986 13 1-000429 35 1-005697 TABLE 22.— REDUCTION OF WATER PRESSURE TO MERCURIAL PRESSURE. aq. 1 Hg. aq. Hg. aq. Hg. aq. Hg. aq. Hg. 0-07 23 1-70 45 3-32 67 4-94 89 6-57 2 0-16 24 1-77 46 3-39 68 6-02 90 6-64 3 0-22 25 1-84 47 3-47 69 5-09 91 6-72 4 0-30 26 1-92 48 3-64 70 6-17 92 6-79 5 0-37 27 1-98 49 3-62 71 5-24 93 6-86 6 0-44 28 2-07 50 3-69 72 5-31 94 6-94 7 0-52 29 2-14 61 3-76 73 5-39 95 7-01 8 0-59 30 2-21 52 3-84 74 5-46 96 7-08 9 0-66 31 2-29 53 3-91 75 6-64 97 7-16 10 0-74 32 2-36 54 3-99 76. 5-61 98 7-23 11 0-81 33 2-44 55 4-06 77 5-68 99 7-31 12 0-89 34 2-61 56 4-13 78 5-76 100 7-38 • 13 0-96 35 2-58 67 4-21 79 6-83 200 14-76 14 1-03 36 2-66 68 4-28 80 5-90 300 22-14 15 1-12 37 2-73 59 4-35 81 5-98 400 29-52 Ifi 1-18 38 2-80 60 4-43 82 6-05 600 36-90 17 1-26 39 2-88 61 4-50 83 6-13 600 44-28 18 1-33 40 2 95 62 4-58 84 6-20 700 51-66 19 1-40 41 3-03 63 4-65 85 6-27 800 59 04 20 1-48 42 3-10 64 4-72 86 6-35 900 66-42 21 1-55 43 3-17 65 4-80 87 6-42 1000 73-80 22 1-62 44 3-25 66 4-87 88 6-49 52 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 23.— TENSION OP AQUEOUS VAPOUR Between -20° and +118° O. in Millimetres Mercury. (Magnus.) T. mm. T. mm. T. mm. -20° 0-916 + 15° 12-677 + 50° 92-0 19 0-999 16 13-519 51 96-6 18 1-089 17 14-409 52 101-5 17 1-186 18 15-351 53 106-6 16 1-290 19 16-345 54 111-9 15 1-403 20 17-396 55 117-4 14 1-525 21 18-505 56 123-1 13 1-655 22 19-675 57 129-1 12 1-796 23 20-909 58 135-3 11 1-947 24 22-211 59 141-8 10 2-109 25 23-582 60' 148-6 9 2-284 26 25-026 61 155-6 8 2-471 27 26-547 62 162-9 7 2-671 28 28-148 63 170-5 6 2-886 29 29-832 64 178-4 S 3-110 30 31-602 65 186-6 i 3-361 31 33-5 66 195 -] 3 3-624 32 35-4 67 204-0 2 3-900 33 37-5 68 213-2 1 4-205 34 39-6 69 222-7 4-525 35 41-9 70 232-6 + 1 4-867 36 44-3 71 242-9 2 5-231 37 46-8 72 253-5 3 5-619 38 49-4 73 264-6 4 6-032 39 .52-1 74 276-0 5 6-471 40 55-0 75 287-9 6 6-939 41 58-0 76 300-2 7 7-436 42 61-1 77 312-9 8 7-964 43 64-4 78 326-1 9 8-525 44 67-8 79 339-8 10 9-126 45 71-4 80 353-9 11 9-756 46 75-2 81 368-6 12 10-421 47 79-1 82 383-7 13 11-130 48 83-2 83 399-4 14 11-882 49 87-5 84 415-6 TENSION OF AQUEOUS VAPOUR TABLE iS—Continued. 53 T. mm. T. mm. T. mm. + 85° 432-3 + 97° 681-7 + 109° 1041-3 86 449-6 98 707-0 110 1077-3 87 467-5 99 733-1 111 1114-3 88 486-0 100 760-0 112 1152-3 89 505-0 101 787-7 113 1191-4 90 524-8 102 816-3 114 1231-7 91 545-1 103 845-7 115 1273-0 92 566-1 104 876-0 116 1315-5 93 587-8 105 907-1 H7 1359-1 94 610-2 106 939-2 118 1403-9 95 633-3 107 972-3 96 657-1 108 1006-3 TABLE 24.— TENSION OF AQUEOUS VAPOUR FOR TEMPERATURES FROM 40° 0. Temperature Tension in mm. Pressure Pressure per sq.om. Centigrade. of Mercury. in atmospheres. in kilos. + 40° 54-906 0-072 0-07465 45 71 -391 0-094 0-09706 50 91-982 0-121 0-12505 55 117-478 0-154 0-15972 60 148-791 0-196 0-20323 66 186-945 0-246 0-25417 70 233-093 0-306 0-31692 75 288-517 0-380 0-39227 80 354-643 0-466 0-48217 85 433-04] 0-570 0-58877 90 525-450 0-691 0-71440 95 633-778 0-834 0-86168 100 760-00 1-000 1-03330 105 906-41 1-193 1-23236 110 1075-37 1-415 1-46210 115 1269-41 1-673 1-72592 120 1491-28 1-962 2-02755 125 1743-88 2-294 2-37098 130 2030-28 2-671 2-76037 135 2353-73 3-097 . 3-20013 54 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 2i— Continued. Temperature Tension in mm. Pressure Pressure per sq.cm. Ceutigrade. of Mercury. in atmospheres. in kilos. + 140° 2717-63 3-575 3-69490 145 3125-55 4-112 4-24960 150 3581-23 4-712 4-86904 155 4088-56 5-380 6-55881 160 4651-62 6-120 6-32434 165 5274-54 6-940 7-17127 170 5961-66 7-844 8-10547 175 6717-43 8-838 9-13302 180 7646-39 9-929 10-2601 185 8453-23 11-122 11-4930 190 9442-70 12-424 12-8383 195 10519-73 13-841 14-3026 200 11688-96 16-380 15-8923 205 12955-66 17-047 17-6145 210 14324-80 18-848 19-4760 215 15801-33 20-791 21-4835 220 17390-00 22-881 23-6439 225 19097-04 26-127 25-9643 230 20926-40 27-534 28-4615 1 Temperature Tension in inches Pressure Pressure in lbs. per Falirenheit. of Mercury. in atmospheres. square inch. 100° 1-918 •064 •941 110 2 -.577 •086 1-267 120 3-427 •114 1^676 130 4-502 •150 2^205 140 5-858 •196 2-883 150 7-546 •252 3-705 160 9-628 •322 4-734 170 12-18 •407 6-984 180 15-27 ■610 7-498 190 19-01 ■636 9-336 200 23-46 •784 11-53 212 29-92 1-000 14-706 220 35-01 1-170 17-19 230 42-34 1-416 20-80 240 60-89 1-701 25-01 TENSION OF AQUEOUS VAPOUR TABLE Z4— Continued. 55 Tempsrature Tension in inches Pressure Pressure in lbs per Fahrenheit. of Mercury. in atmospheres. square inch. 250° 60-81 2-032 29-87 260 72-27 2-415 35-50 270 85-41 2-855 41-97 280 100-4 3-366 49-34 290 117-5 3-927 57-73 300 136-8 4-572 67-22 310 158-6 5-301 77-94 320 183-1 6-120 89-98 330 210-5 7-035 103-4 340 241-1 8-058 118-5 350 275-0 9-198 135-2 360 312-6 10-45 153-6 370 354-0 11-83 173-9 380 399-6 13-35 196-3 390 449-6 15-02 220-8 400 504-4 16-86 247-9 410 563-9 18-84 277-0 420 628-8 21-01 309-9 430 699-2 23-37 843-6 440 775-3 25-91 380-9 TABLE 25.— TENSION OP AQUEOUS VAPOUR IN INCHES OP MERCURY PROM 1° TO 100° P. Temperature Inches of Temperature Inches of Fahrenheit. Mercury. Fahrenheit. Mercury. 1° -046 11° ■071 2 ■048 12 •074 3 •050 13 •078 4 ■052 14 •082 5 •054 15 •086 6 •057 16 •090 7 •060 17 ■094 8 •062 18 •098 9 •065 19 •103 10 •068 20 ■108 56 THE TECHNICAL CHEMISTS' HANDBOOK TABLE ih—Gontimied. Temperature Inches of Temperature Inches of Fahrenheit. Mercury. Fahrenheit. Mercury. 21° •113 61° ■537 22 •118 62 •556 23 •123 63 •576 24 •129 64 •596 25 ■135 66 •617 26 •141 66. ■639 27 •147 67 ■661 28 •163 68 ■685 29 •160 69 ■708 30 •167 70 ■733 31 •174 71 •759 32 •181 72 •785 33 •188 73 ■812 34 ■196 74 ■840 35 •204 75 ■868 36 •212 76 ■897 37 ■220 77 ■927 38 •229 78 •958 39 •238 79 •990 40 •247 80 1^023 41 •257 81 1-067 42 •267 82 1-092 43 •277 83 1-128 44 •288 84 1^165 45 •299 85 1-203 46 •311 86 1-242 47 •323 87 1^282 48 ■335 88 1-323 49 ■348 89 1^366 60 ■361 90 1^401 51 •374 91 1^455 52 ■388 92 1-501 53 ■403 93 1-648 54 ■418 94 1-696 55 ■433 95 1-646 66 ■449 96 1-697 67 ■465 97 1-751 58 •482 98 1-806 59 ■600 99 1-862. 60 ■618 100 1-918 BOILING POINT OF WATER, ETC. 57 TABLE 26.— BOILING POINT OP WATER AT DIFFERENT BAROMETRIC PRESSURES. Barometric Boiling Barometric Boiling Pressure. Point. Pressure. Point. mm. mm. 710 98-11 , 745 99-44 71.5 98-30 750 99-63- 720 98-49 755 99-82 725 98-69 760 100-00 730 - 98-88 . 765 100-18 735 99-07 770 100-37 740 99-26 775 100-55 TABLE 27.— SPECIFIC HEATS. (a) Of Solids and Liquids. Aluminium 0-2220 Iron (cast) . 0-1050 Alcohol 0-547 (wrought) . 0-1081 Antimony . 0-0493 Lead . . . 0-0309 Ashes 0-20 Limestone (marble) 0-21 Bismuth . 0-0303 Mercury . 0-0334 Brass . 0-0917 Nickel . 0-109 Bricks 0-22 Oil (lubricating) 0-40 Cement 0-19 Platinum . 0-0324 Carbon (wood) 0-1653 Sandstone . 0-22 (graphitf ; . 0-1604 Slag . . . 0-18 (diamon J) . 0-1042 Silver 0-0559 Copper 0-0936 Steel . 0-1070 Glass (for therm ometers) 0-1988 Sulphur 0-1764 Gypsum . 0-20 Sulphuric acid . 0-332 Granite 0-20 Tin . . . 0-0552 Gold . 0-0316 Zinc . 0-0935 (6) Of Gases and Vapours for Constant Pressures between the Temperatures of 0° and 200° C. (Lansen and Regnault.) Cal. per Cal. per Cal. per Cal. per 1kg. 1 cb.m. 1kg. 1 cb.m. Atmospheric air . 0-2389 0-3082 Carbon monoxide 0-2466 0-3082 Oxygen 0-2158 0-3082 Methane 0-5930 0-4241 Nitrogen 0-2459 0-3082 Ethylene 0-4040 0-6053 Hydrogen 3-452 0-3082 Sulphur dioxide . 0-1544 0-4413 Carbon dioxide . 0-2092 0-4109 Aqueous vapour . 0-4542 0-3654 58 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 28.— HEATING BPPECTS. (a) Definitions. A metrical gram-ealorle (cal. ) is the quantity of heat required to raise the temperature of 1 gram of water 1° 0. The kilogram- calorie = 1000 cal. The normal calorie is that which raises 1 gram water of 14 "5° to 15-5° C. The Britisli heat unit is the quantity of heat required to raise the temperature of 1 pound of water from 32° to 33° Fahr., and is = 252 gram-calories. This unit is required only where the absolute values of the heat units are considered. Usually the question is only of relative values — e.g., grams or pounds of fuel on the one hand, against grams or pounds of water on the other. For these compari- sons the simple proportion of British heat units to gram-calories = 5:9 is used, as the unit of fuel weight is the same as that of the water, and only the degrees Centigrade and Fahrenheit differ as above. 1 British heat unit is, therefore, = f = 0-5656 gram-calorie. 1 Joule (j) = 10 million ergs = 0-2391 gram-calorie. 1 Gram-calorie = 4-183 j. IJ = 1000 j = 239-1 cal. = 10" erg. (6) Calorific Value of Fuels. (The data given are the upper heating values, j. e. , they are referred to the combustion of hydrogen to liquid water as found in the calorimeter.) met, cal. Ether . 9,000 Alcohol . . 7,100 Lignite-tar oil . . 9,950 Wood . 4,100 Methyl alcohol . . 5,300 Charcoal (C to COg) . . 8,000 „ (CtoCO) . . 2,300 met. cal. Petroleum residue . 10,500 Petroleum . 11,000 Fatty oils . . 9,300 Tallow . 8,370 Beeswax . . 9,000 Cellulose . . 4,200 (c) Calorific Value of G-ases. ! 2 16 28 78 128 28 Moleo. Calories when burnt to Calories per cub. met. when burnt to Liquid Water. Steam. Liquid Water. Steam. Hydrogen, Hj . Methane, CH- . Ethylene, C2H4 Benzene vapour, CuH,, Naphthalene vapour, CuHg Carbon monoxide, CO 69-0 213-5 334-S 788-0 1258-4 68-4 58-1 192-1 313-4 755-9 1230-6 68-4 3064 9566 14,999 35,302 56,376 3064 2585 8606 14,060 33,864 55,131 3064 AIR COMPRESSION 59 TABLE 29.— AIR COMPRESSION. The following table is compiled with a view to facilitate calculations of problems connected with the application of compressed gases. The table is strictly correct only for air, but is applicable also to other gases,' such as lime-kiln gases. The table relates to 1 cub. foot of atmospheric air measured at 60° F. and 29-92 inches barometric pressure, and shows the volumer"£emperature, and pressure after adiabatic compr^sion ; also the height of a column of water which the compressed gas will just balance, and the power required to compress the air in foot-pounds (33,000 ft. -lbs. per minute = 1 indicated horse-power), and the mean pressure on the air piston. Final Pressure lbs. per sq. in. above Atmosphere. Column of Water tlie Volume of compressed Temperature after Mean Pressure on Foot-pounds of Work per balance. Air. Compression. Piston. cub. foot atmosph. air. Lbs. Feet. Cub. feet. Degrees F. Lbs.persq.in. 10 23-12 0-692 144-5 8-23 1186-3 12 27-75 0-655 158-1 9-58 1387 14 32-87 0-622 171-0 10-86 1564 16 87-00 0-593 184-0 12-08 1739 18 41-62 0-567 196-0 13-23 1907 20 46-25 0-544 207-3 14-35 2066 22 50-87 0-623 218-8 16-42 2220 24 55-60 0-504 228-6 16-45 2368 26 60-12 0-486 239-0 17-48 2510 28 64-75 0-469 249-0 18-39 2647 30 69-37 0-454 258-2 19-32 2782 82 74-00 0-440 267-5 20-21 2910 34 78-62 0-428 276-4 21-07 3034 86 83-25 0-416 285-3 21-92 3156 38 87-87 0-404 293-5 22-74 3275 40 92-50 0-394 301-8 23-63 3389 In Metrical Units. Final Pressure above 1 atm. per sq.cm. Column of Water the Gas will balance. Volume of 1 cub.m. air after Com- pression. Temperature after Compression. Mean Pressure on Piston. Work per 1 cub.m. in metre-kg. Kg. m. cub.m. •c. Kg. per sq.cm. 0-703 7-05 0-692 62-5 0-679 5,789 0-844 8-44 0-665 70-1 0-674 6,769 0-984 9-87 0-622 77-2 0-764 7.633 1-125 11-28 0-593 84-4 0-849 8,48« 1-266 12-69 0-567 91-1 0-930 9,307 60 THE TECHNICAL CHEMISTS" HANDBOOK TABLE Zd—Contimied. Final Pressure above 1 atm. per sq.cm. Column of Water the Gas will balance. Volume of 1 cub. m. air after Ck)m- pression. Temperature after OompresBion. Mean Pressure on Piston. Work per 1 cub.tn. in metre- leg. Kg. ' 14-10 cub.m. -0. Kg.persq.cni. 1-406 0-544 97-4 1-009 9,791 1-547 15-50 0-523 103-5 1-084 10,835 1-687 16-91 0-504 109-2 1-157 11,557 1-828 18-32 0-486 115-9 1-226 12,251 1-969 19-74 0-469 120-6 1-293 12,919 2-109 21-14 0-454 125-7 1-358 13,573 2-250 22-55 0-440 130-8 1-421 14,203 2-391 . 23-96 0-428 135-8 1-481 14,808 2-531 25-37 0-416 140-7 1-541 15,403 2-374 26-78 0-404 145-4 1-599 15,984 2-812 28-19 0-394 149-9 1-654 16,541 TABLE 30.— EXPLOSIVE MIXTURES OP GASES AND AIR. (Eitner.) Volumes of Gas. Volumes of Air. Acetylene 3-5-52-2 96-5-47-8 Hydrogen . 9-5-66-3 90-5-3S-7 Carbon monoxide 16-6-74-8 83-4-25-2 Ethylene . 4-2-14-5 95-8-85-5 Methane . 6-2-12-7 93-8-87-3 Coal-gas 8-0-19 92-0-81 Benzene vapour . 2-7- 6-3 97-3-93-7 Petroleum spirit vapour 2-5- 4-8 97-5-95-2 F.tlier 2.-9- 7-0 97-1-92-5 PROPERTIES OF THE LIQUEFIED GASES 61 o II ni psjmbgj qs9^ oqijonoBBodoa Tti -* (N (M ■* a §!■ SB V HV StOSSBA am JO {)B9} ISPBO ^ 00 1-1 T-H (N CO CO las .-iX A ■^o •90UB{^B S rfl ■:o ^ -qns -Sii I loj ^ CO 00 OO OO 9osds p9qyos9Ja lA I-l I-( o o l-t o 1>- fM •^niod SnHieji 9 o l-H 1 i 1 O 1 1 CS (N I-l CD (N c*a CO *gans&9id 'nini 09i ;b wod Sniipa 9 OO 1 00 1 O 1 CO CO 1 ■ OO CO 1 00 + lO OO 1 1 OS un ■Mnsseid (bomi^D ^ CO OO CO id (M lO ■<1» ^ ■* lO m i-H ITS «o o -«}* OO ■8IIHE19dni9} ITOIJIIO o D3 CO 1-1 CO CO i-l 1 1 JO BtnniOA sb3 b = o CO I-l o OO lO l~^ -* § g OO CO -* OO iH : i- OO (M t- CO T-l M a en (N (N un t^ 1^ rH • o CO W CO Tj* (N eCi ica 2 i>. > 2 o .—1 1-H o O ■<*< to IX) Tji Mjj !>. CO OS CM „« lO 00 OO CO '^ «D, o o rH ,—1 O t^ l>- W OO -* CI CO tH CO -© CO m b V' OS ■* ■* «D ■* o o 1-1 l-H o y-i -s • 1 to g 1 § 1 hi S -G -a * c 1 J3 .S2 '5 o B a Is z o co- O < £ ffi O 62 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 32.— ELECTRICAL UNITS. 1. The unit of quantity, the coulomb, is that quantity of current which precipitates I'llS mg. silver from a solution of silver nitrate. 2. The unit of current, the ampere, is that current which conveys 1 coulomb through the circuit in 1 second. 1 ampere-hour is = the quantity of current which gives per hour 1 ampere, or per n hours, — amperes = 3600 coulombs. n 3. The unit of resistance, the olim, is equal to the resistance of a column of mercury at 0° C. of a sectional area of 1 x 1 mm., 106 '3 cm. long, possessing a mass of 14-4251 grams. Other units in use are the Siemens unit=0-944 ohm, and the British Association unit (B.A.U.) = 0-989 ohm. 4. The unit of electromotive force, the volt, is the force which in a conductor with a resistance of 1 ohm gives a current = 1 ampere. Electromotive force of a Daniell cell = 1-12 volts. „ „ Bunsen cell = 2 volts. Clark ceU = 1-4328 volts. Weston cell = 0-0186 volt. ,, „ lead storage cell = 2-1-1-9 volts. 6. The farad is the capacity of a condenser in which a charge of 1 coulomb produces a difference of potential of 1 volt. 6. A -watt or volt-ampere is the amount of work produced during 1 second by a current of 1 ampere under an electromotive force of 1 volt. It is = 1 metre-kilogram ^^^^^ ^ g.^^g ^^.j^ ^^^^^ ^ 9-81 ^ horse-power = 735-5 watts. The British Board of Trade Unit is = 1000 watt hours. 1 kilowatt (kw) = 1000 watts = 1-36 horse-power. A current of 1 ampere, at a resistance of w ohms, produces during t seconds a quantity of heat = 0-239 wt gram-calorie. 1 cal. = 4-19 joules. TABLE 33.— ELECTRO-CHEMICAL EQUIVALENTS. The separation of a gram equivalent requires 96,540 coulombs = 26-86 ampere hours. 1 ampere hour is capable of yielding : — Grams. Grams. Silver . ... 4-0228 Ohlorine . 1-B228 Copper (from solutions ot oapric salts) 1-1862 Bromine . 2-982 Zinc ... 1-219 Iodine . 4-7828 Nickel . ... 1-0941 Oxygen . 0-2983 Hydrogen ..... 0376 Potassium chlorate 0-7618 Alnminium 0-3369 Potassium hydroxide . 2094 Lead 8-862 Sodium hydroxide 1-494 Gold 2-4612 Potassinm 1-4680 '■ Hagnesium 0-4534 Platinum 3-6396 Mercury ... 8-7290 Tin 2-2188 MATHEMATICAL TABLES 63 TABLE 34.— MATHEMATICAL TABLES. Circumference and area of circles, squares, cubes, square and cube roots. n Til O • »2 «» s/n ^n 1-0 3-142 0-7854 1-000 1-000 1-0000 1-0000 1-1 3-456 0-9503 1-210 1-331 1-0488 1-0323 1-2 3-770 1-1310 1-440 1-728 1-0955 1-0627 1-3 4-084 1-3273 1-690 2-197 1-1402 1-0914 1-4 4-398 1-5394 1-960 2-744 1-1832 1-1187 1-5 4-712 1-7672 2-250 3-375 1-2247 1-1447 1-6 5-027 2-0106 2-560 4-096 1-2649 1-1696 1-7 5-341 2-2698 2-890 4-913 1-3038 1-1935 1-8 5-655 2-5447 3-240 5-832 1-3416 1-2164 1-9 5-969 2-8353 3-610 6-859 1-3784 1-2386 2-0 6-283 3-1416 4-000 8-000 1-4142 1-2599 2-1 6-597 3-4636 4-410 9-261 1-4491 1-2806 2-2 6-912 3-8013 4-840 10-648 1-4832 1-3006 2-3 7-226 4-1548 5-290 12-167 1-5166 1-3200 2-4 7-640 4-5239 5-760 13-824 1-5492 1-3389 2-5 7-854 4-9087 6-250 15-625 1-5811 1-3572 2-6 8-168 5-3093 6-760 17-576 1-6126 1-3761 2-7 8-482 5-7256 7-290 19-683 1-6432 1-3925 2-8 8-797 6-1575 7-840 21-952 1-6733 1-4095 2-9 9-111 6-6052 8-410 24-389 1-7029 1-4260 3-0 9-425 7-0686 9-00 27-000 1-7321 1-4422 3-1 9-739 7-5477 9-61 29-791 1-7607 1-4581 3-2 10-053 8-0426 10-24 32-768 1-7889 1-4736 3-3 10-367 8-5530 10-89 35-937 1-8166 1-4888 3-4 10-681 9-0792 11-66 39-304 1-8439 1-5037 3-5 10-996 9-6211 12-25 42-875 1-8708 1-5183" 3-6 11-310 10-179 12-96 46-666 1-8974 1-5326 3-7 11-624 10-752 13-69 50-653 1-9235 1-5467 3-8 11-938 11-341 14-44 54-872 1-9494 1-5605 3-9 12-252 11-946 15-21 59-319 1-9748 1-5741 4-0 12-566 12-566 16-00 64-000 2-0000 1-5874 4-1 12-881 13-203 16-81 68-921 2-0249 1-6006 4-2 13-195 13-854 17-64 74-088 2-0494 1-6134 4-3 13-509 14-522 18-49 79-507 2-0736 1-6261 4-4 13-823 15-205 19-36 85-184 2-0976 1-6386 4-5 14-137 15-904 20;25 91-125 2-1213 1-6510 4-6 14-451 16-619 21-16 97-336 2-1448 1-6631 4-7 14-765 17-349 22-09 103-823 2-1680 1-6751 64 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 34:— Continued. m2 n O IT 4 • »» ■n? s/^T V^ 4-8 15-080 18-096 23-04 110-592 2-1909 1-6869 4-9 15-394 18-857 24-01 117-649 2-2136 1-6985 5-0 15-708 19-635 25-00 125-000 2-2361 1-7100 5-1 16-022 20-428 26-01 132-651 2-2583 1-7213 5-2 16-336 21-237 27-04 140-608 2-2804 1-7325 5-3 16-650 22-062 28-09 148-877 2-3022 1-7435 5-4 16-965 22-902 29-16 157-464 2-3238 1-7544 5-0 17-279 23-758 30-25 166-375 2-3452 1-7652 5-6 17-593 24-630 31-36 175-G16 2-3664 1-7758 5-7 17-907 25-518 ' 32-49 185-193 2-3875 1-7863 5-8 18-221 26-421 33-64 195-112 2-4083 1-7967 5-9 18-535 27-340 34-81 205-379 2-4290 1-8070 6-0 18-850 28-274 36-00 216-000 2-4495 1-8171 6-1 19-164 29-225 37-21 226-981 2-4698 1-8272 6-2 19-478 30-191 38-44 238-328 2-4900 1-8371 6-3 19-792 31-173 39-69 250-047 2-5100 1-8469 6-4 20-106 32-170 40-96 262-144 2-5298 1-8566 6-5 20-420 33-183 42-25 274-625 2-5495 1-8663 6-6 20-735 34-212 43-56 287-496 2-5691 1-8758 6-7 21-049 35-257 44-89 300-763 2-6884 1-8852 6-8 21-363 36-317 46-24 314-432 2-6077 1-8945 6-9 21-677 37-393 47-61 328-509 2-6268 1-9038 7-0 21-991 38-485 49-00 343-000 2-6458 1-9129 7-1 22-305 39-592 50-41 357-911 2-6646 1-9920 . 7-2 22-619 40-715 51-84 373-248 2-6833 1-9310 7-3 22-934 41-854 53-29 389-017 2-7019 1-9399 7-4 23-248 43-008 54-76 405-224 2-7203 1-9487 7-5 23-562 44-179 56-25 421-875 2-7386 1-9574 7-6 23-876 45-365 57-76 438-976 2-7568 1-9661 7-7 24-190 46-566 59-29 456-533 2-7749 1-9747 7-8 24-504 47-784 60-84 474-552 2-7929 1-9832 7-9 24-819 49-017 62-41 493-039 2-8107 1-9916 8-0 25-133 50-266 64-00 512-000 2-8284 2-0000 8-1 25-447 51-530 65-61 531-441 2-8461 2-0083 8-2 25-761 52-810 67-24 551-368 2-8636 2-0165 8-3 26-075 54-106 68-89 571-787 2-8810 2-0247 8-4 26-389 55-418 70-56 592-704 2-8983 2-0328 MATHEMATICAL TABLES TABLE 34— Continued. 65 n 7r« O • «2 „3 \/« ^« 8-5 26-704 56-745 72-25 614-125 2-9155 2-0408 8-6 27-018 58-088 73-96 636-056 2-9326 2-0488 8-7 27-332 59-447 75-69 658-503 2-9496 2-0567 8-8 27-646 60-821 77-44 681-472 2-9665 2-0646 8-9 27-960 62-211 79-21 704-969 2-9833 2-0724 9-0 28-274 63-617 81-00 729-000 3-0000 2-0801 9-1 28-588 65-039 82-81 753-671 3-0166 2-0878 9-2 28-903 66-476 84-64 778-688 3-0332 2-0964 9-3 29-217 67-929 86-49 804-357 3-0496 2-1029 9-4 29-531 69-39b 88-36 830-584 3-0659 2-1105 9-5 29-845 70-882 90-25 857-375 3-0822 2-1179 9-6 30-159 72-382 92-16 884-736 3-0984 2-1253 9-7 30-473 73 -SO,- 94-09 912-673 3-1146 2-1327 9-8 30-788 75,-430 96-04 941-192 3-1305 2-1400 9-9 31-102 76-977 98-01 970-299 3-1464 2-1472 10-0 31-416 78-540 100-00 1000-000 3-1623 2-1544 10-1 31-730 80-119 102-01 1030-301 3-1780 2-1616 10-2 32-044 81-713 104-04 1061-208 3-1937 2-1687 10-3 32-358 83-323 106-09 1092-727 3-2094 2-1757 10-4 32-673 84-949 108-16 1124-864 3-2249 2-1828 10-5 32-987 86-590 110-25 1157-625 3-2404 2-1897 10-6 33-301 88-247 112-36 1191-016 3-2568 2-1967 10-7 33-615 89-920 114-49 1225-043 3-2711 2-2036 10-8 33-929 91-609 116-64 1259-712 3-2863 2-2104 10-9 34-243 93-313 118-81 1295-029 3-3015 2-2172 11-0 34-558 95-033 121-00 1331-000 3-3166 2-2239 11-1 34-872 96-769 123-21 1367-631 3-3317 2-2307 11-2 35 •186 98-520 125-44 1404-928 3-3466 2-2374 11-3 35-500 100-29 127-69 1442-897 3-3615 2-2441 11-4 35-814 102-07 129-96 1481-544 3-3754 2-2506 11-5 36-128 103-87 132-25 1520-875 3-3912 2-2572 11-6 36-442 105-68 134-56 1560-896 3-4069 2-2637 11-7 36-757 107-51 136-89 1601-613 3-4206 2-2702 11-8 37-071 109-36 139-24 1643-032 3-4361 2-2766 11-9 37-385 111-22 141-61 1685-159 3-4496 2-2831 12-0 37-699 113-10 144-00 1728-000 3-4641 2-2894 12-1 38-013 114-99 146-41 1771-561 3-4785 2-2957 12-2 38-327 116-90 148-84 1816-848 3-4928 2-3021 66 THE TECHNICAL CHEMISTS' HANDBOOK TABLE Zi—Gontinmd. n irn O "4- • n? ns ijn v/» 12-3 38-642 118-82 151-29 1860-867 3-5071 2-3084 12-4 38-956 120-76 153-76 1906-624 3-5214 2-3146 12-5 39-270 122-72 156-.15 1953-125 3-5355 2-3208 12-6 39-584 124-69 158-76 2000-376 3-5496 2-3270 12-7 39-898 126-68 161-29 2048-383 3-5637 2-3331 12-8 40-212 128-68 163-84 2097-152 3-5777 2-3392 12-9 40-527 130-70 166-41 2146-689 3-5917 2-3453 13-0 40-841 132-73 169-00 2197-000 3-6056 2-3513 13-1 41-155 134-78 171-61 2248-091 3-6194 2-3573 13-2 41-469 136-85 174-24 2299-968 3-6332 2-3633 13-3 4] -783 138-93 176-89 2352-637 3-6469 2-3693 13-4 42-097 141-03 179-56 2406-104 3-6606 2-3752 13-5 42-412 143-14 182-25 2460-375 3-6742 2-3811 13-6 42-726 145-27 184-96 2515-456 3-6878 2-3870 13-7 43-040 147-41 187-69 2571-353 3-7013 2-3928 13-8 43-354 149-57 190-44 2628-072 S-7148 2-3986 13-9 43-668 151-75 193-21 2685-619 3-7283 2-4044 14-0 43-892 153-94 196-00 2744-000 3-7417 2-4101 14-1 44-296 156-15 198-81 2803-221 3-7550 2-4159 14-2 44-611 158-37 201-64 2863-288 3-7683 2-4216 14-3 44-925 160-61 204-49 2924-207 3-7815 2-4272 14-4 45-239 162-86 207-36 2985-984 3-7947 2-4329 14-5 45-553 165-13 210-25 3048-625 3-8079 2-4385 14-6 45-867 167-42 213-16 3112-136 3-8210 2-4441 14-7 46-181 169-72 216-09 3176-623 3-8341 2-4497 14-8 46-496 172-03 219 04 3241-792 3-8471 2-4552 14-9 46-810 174-37 222-01 3307-949 3-8600 2-4607 15-0 47-124 176-72 225-00 3375-000 3-8730 2-4662 15-1 47-438 179-08 228-09 3442-951 3-8859 2-4717 15-2 47-752 181-46 231-04 3511-808 3-8987 2-4772 15-3 48-066 183-85 234-09 3581-577 3-9115 2-4825 15-4 48-381 186-27 237-16 3652-264 3-9243 2-4879 15-5 48-695 188-69 240-25 3723-875 3-9370 2-4933 15-6 49-009 191-13 243-36 3796-416 3-9497 2-4986 15-7 49-323 193-59 246-49 3869-893 3-9623 2-5039 IS -8 49-637 196-07 249-64 3944-312 3-9749 2-5092 15-9 49-951 198-56 252-81 4019-679 3-9875 2-5146 MATHEMATICAL TABLES TABLE Z4:— Continued. 67 ft 16-0 7r» O • tfi n? n/» V» 50-265 201-06 256-00 4096-000 4-0000 2-6198 16-1 50-580 203-58 259-21 4173-281 4-0125 2-6251 16-2 50-894 206-13 262-44 4251-628 4-0249 2-5303 16-3 51-208 208-67 266-69 4330-747 4-0373 2-5355 16-4 51-522 211-24 268-56 4410-944 4-0497' 2-5406 16-5 61-836 213-83 272-25 4492-125 4-0620 2-5458 16-6 52-150 216-42 275-56 4574-296 4-0743 2-5509 16-7 52-465 219-04 278-89 4657-463 4-0866 2-5561 16-8 52-779 221-67 282-24 4741-632 4-0988 2-5612 16-9 53-093 224-32 285-61 4826-809 4-1110 2-6663 17-0 53-407 226-98 299-00 4913-000 4-1231 2-6713 17-1 53-721 229-66 292-41 5000-211 4-1352 2-5763 17-2 54-035 232-35 295-84 5088-448 4-1473 2-5813 17-3 54-350 235-06 299-29 5177-717 4-1593 2-5863 17-4 54-664 237-79 302-76 5268-024 4-1713 2-5913 17-5 54-978 240-53 306-25 5359-375 4-1833 2-5963 17-6 55-292 243-29 309-76 5451-776 4-1952 2-6012 17-7 65-606 246-06 313-29 5545-233 4-2071 2-6061 17-8 55-920 248-85 316-84 5639-752 4-2190 2-6109 17-9 56-235 251-65 320-41 6735-339 4-2308 2-6158 18-0 56-549 254-47 324-00 5832-000 4-2426 2-6207 18-1 56-863 257-30 327-61 5929-741 4-2544 2-6256 18-2 57-177 260-16 331-24 6028-568 4-2661 2-6304 18-3 57-491 263-02 334-89 6128-487 4-2778 2-6352 18-4 57-805 265-90 338-56 6229-504 4-2896 2-6400 18-5' 58-119 268-80 342-25 6331-625 4-3012 2-6448 18-6 58-434 271-72 345-96 6434-856 4-3128 2-6495 18-7 58-748 274-65 349-69 6539-203 4-3243 2-6543 18-8 59-062 277-69 353-44 6644-672 4-3459 2-6590 18-9 59-376 280-55 357-21 6751-269 4-3474 2-6637 19-0 59-690 283-63 361-00 6869-000 4-3589 2-6684 19-1 60-004 286-52 364-81 6967-871 4-3703 2-6731 19'2 60-319 289-63 368-64 7077-888 4-3818 2-6777 19-3 60-633 292-65 372-49 7189-057 4-3942 2-6824 19-4 60-947 295-59 376-36 7301-384 4-4045 2-6869 19-5 61-261 298-65 380-26 7414-875 4-4159 2-6916 19-6 61 -575 301 -72 384-16 7629-536 4-4272 2-6962 19-7 61-889 304-81 388-09 7642-373 4-4385 2-7008 68 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 3i— Continued. n irn O 4 • B- n> ^ 19-8 62-204 307-91 392-04 7762-392 4-4497 2-7053 19-9 62-518 311-03 396-01 7880-599 4-4609 2-7098 20-0 62-832 314-16 400-00 8000-000 4-4721 2-7144 20-1 63-146 317-31 404-01 8120-601 4-4833 2-7189 20-2 63-460 320-47 408-04 8242-408 4-4944 2-7234 20-3 63-774 323-66 412-09 8365-427 4-6055 2-7279 20-4 64-088 326-85 416-16 8489-664 4-5166 2-7324 20-5 64-403 330-06 420-25 8615-125 4-5277 2-7368 20-6 64-717 333-29 424-36 8741-816 4-5387 2-7413 20-7 65-031 336-54 428-49 8869-743 4-5497 2-7457 20-8 65-345 339-80 432-64 8998-912 4-5607 2-7502 20-9 65-659 343-07 436-81 9129-329 4-5716 2-7545 21-0 65-973 346-36 441-00 9261-000 4-5826 2-7589 21-1 66-288 349-67 445-21 9393-931 4-5935 2-7633 21-2 66-602 352-99 449-44 9528-128 4-6043 2-7676 21-3 66-916 356-33 453-69 9663-597 4-6152 2-7720 21-4 67-230 359-68 457-96 9800-344 4-6260 2-7763 21-5 67-544 363-05 462-25 9938-375 4-6368 2-7806 21-6 67-858 366-44 466-56 10077-696 4-6476 2-7849 21-7 68-173 369-84 470-89 10218-313 4-6583 2-7893 21-8 68-487 373-25 475-24 10360-232 4-6690 2-7935 21-9 68-801 376-69 479-41 10503-459 4-6797 2-7978 22-0 69-115 380-13 484-00 10648-000 4-6904 2-8021 22-1 69-429 383-60 488-41 10793-861 4-7011 2-8063 22-2 69-743 387-08 492-84 10941-048 4-7117 2-8105 22-3 70-058 390-57 497-29 11089-567 4-7223 2-8147 22-4 70-372 394-08 501-76 11239-424 4-7329 2-8189 22-5 70-686 397-61 506-25 11390-625 4-7434 2-8231 22-6 71-000 401-15 510-76 11543-176 4-7539 2-8273 22-7 71-314 404-71 515-29 11697-083 4-7644 2-8314 22-8 71-628 408-28 519-84 11852-352 4-7749 2-8356 22-9 71-942 411-87 524-41 12008-989 4-7854 2-8397 23-0 72-257 415-48 529-00 12167-000 4-7958 2-8438 23-1 72-571 419-10 533-61 12326-391 4-8062 2-8479 23-2 72-885 422-73 538-24 12487-168 4-8166 2-8521 23-3 73-199 426-39 542-89 12649-337 4-8270 2-8562 23-4 73-513 430-05 547-56 12812-904 4-8373 2-8603 MATHEMATICAL TABLES TABLE 3i— Continued. 69 n 7r» O 4 • «» »3 >Jn :/» 23-5 73-827 433-74 • 652-25 12977-875 4-8477 2-8643 23-6 74-142 437 44 566-96 13144-256 4-8680 2-8684 23-7 74-456 441 16 561-69 13312-063 4-8683 2-8724 23-8 74-770 444 88 566-44 13481-272 4-8785 2-8766 23-9 75-084 448 63 571-21 13651-919 4-8888 2-8805 24-0 75-398* 452 39 676-00 13824-000 4-8990 2-8845 24-1 76-712 456 17 580-81 13997-521 4-9092 2-8886 24-2 76-027 459 96 585-64 14172-488 4-9192 2-8925 24-3 76-341 463 77 590-49 14348-907 4-9295 2-8966 24-4 76-655 467 60 596-36 14626-784 4-9396 2-9004 24-5 76-969 471 44 600-25 14706-125 4-9497 2-9044 24-6 77-283 475 29 606-16 14886-936 4-9598 2-9083 24-7 77-697 479 16 610-09 16069-223 4-9699 2-9123 24-8 77-911 483 05 615-04 15252-992 4-9799 2-9162 24-9 78-226 486 96 620-01 15438-249 4-9899 2-9201 25-0 78-540 490 87 626-00 15625-000 6-0000 2-9241 25-1 78-854 494 81 630-01 16813-251 5-0099 2-9279 25-2 79-168 498 76 635-04 16003-008 6-0199 2-9318 25-3 79-482 502 73 640-09 16194-277 5-0299 2-9366 26-4 79-796 506 71 645-16 16387-064 5-0398 2-9395 25 -D 80-111 510 71 650-26 16581-375 6-0497 2-9434 25-6 80-425 514 72 655-36 16777-216 5-0596 2-9472 25-7 80-739 518 75 660-49 16974-593 6-0696 2-9510 25-8 81-053 522 79 665-64 17173-512 6-0793 2-9549 26-9 81-367 526 83 670-81 17373-979 5-0892 2-9586 26-0 81-681 530 93 676-00 17576-000 5-0990 2-9624 26-1 81-996 535 02 681-21 17779-681 5-1088 2-9662 26-2 82-310 639 13 686-44 17984-728 5-1185 2-9701 26-3 82-624 543 25 691-69 18191-447 5-1283 2-9738 26-4 82-938 547 39 696-96 18399-744 5-1380 2-9776 26-6 83-252 551 55 702-25 18609-625 5-1478 2-9814 26-6 83-566 556 72 707-56 18821-096 5-1576 2-9851 26-7 83-881 559 90 712-89 19034-163 5-1672 2-9888 26-8 84-195 564 10 718-24 19248-832 5-1768 2-9926 26-9 84-509 568 32 723-61 19465-109 5-1865 2-9963 27-0 84-823 372 56 729-00 19683-000 5-1962 3-0000 27-1 85-137 576 80 734-41 19902-511 5-2057 3-0037 27-2 85-451 581-07 739-84 20123-648 5-2153 3-0074 70 THE TECHNICAL CHEMISTS' HANDBOOK TABLE U—Contvimed. n O 7r — 4 • ■n? ns ^ U- 27-3 85-765 585-35 745-29 20S46-417 5-2249 3-0111 27-4 86-080 589-65 750-76 2057.0-824 5-2345 3-0147 27-5 86-394 593-96 756-25 20796-875 5-2440 3-0184 27-6 86-708 598-29 761-76 21024-576 5-2535 3-0221 27-7 87-022 602-63 767-29 21253-933 5-2630 3-0257 27-8 87-336 606-99 772-84 21484-952 5-2725 3-0293 27-9 87-650 611-36 778-41 21717-639 5-2820 3-0330 28-0 87-965 615-75 784-00 21952-000 5-2915 3-0366 28-1 88-279 620-16 789-61 22188-041 5-3009 3-0402 28-2 88-593 624-58 795-24 22425-768 5-3103 3-0438 28-3 88-907 629-02 800-89 22665-187 5-3197 3-0474 28-4 89-221 633-47 806-56 22906-304 5-3291 3-0510 28-5 89-535 637-94 812-25 23149-125 5-3385 3-0546 28-6 89-850 642-42 817-96 23393-656 5-3478 3-0581 28-7 90-164 646-93 823-69 23639-903 5-3572 3-0617 28-8 90-478 651-44 829-44 23887-872 5-3665 3-0652 28-9 90-792 665-97 835-21 24137-569 5-3758 3-0688 29-0 91-106 660-52 841-00 24389-000 5-3852 3-0723 29-1 91-420 665-08 846-81 24642-171 5-3944 3-0758 29-2 91-735 669-66 852-64 24897-088 5-4037 3-0794 29-3 92-049 674-26 858-49 25153-757 5-4129 3-0829 29-4 92-363 678-87 864-36 25412-184 5-4221 3-0864 29-5 92-677 683-49 870-25 25672-375 5-4313 3-0899 29-6 92-991 688-13 876-16 25934-336 5-4405 3-0934 29-7 93-305 692-79 882-09 26198-073 5-4497 3-0968 29-8 93-619 697-47 888-04 26463-592 5-4589 3-1003 29-9 93-934 702-15 894-01 26730-899 5-4680 3-1038 30-0 94-248 706-86 900-00 27000-000 5-4772 3-1072 30-1 94-562 711-58 906-01 27270-901 5-4863 3-1107 30-2 94-876 716-32 912-04 27543-608 5-4954 3-1141 30-3 95-190 721-07 918-09 27818-127 5-5045 3-1176 30-4 95-504 725-83 924-16 28094-464 5-5136 3-1210 30-5 95-819 730-62 930-25 28372-625 5-5226 3-1244 30-6 96-133 735-42 936-36 28652-616 5-5317 3-1278 30-7 96-447 740-23 942-49 28934-443 5-5407 3-1312 30-8 96-761 745-06 948-64 29218-112 5-5497 3-1346 30-9 97-075 749-91 954-81 29503-629 5-5587 3-1380 MATHEMATICAL TABLES TABLE Si— Continued. 71 n2 n Trm TT i O • 31-0 97-389 754-77 31-1 97-704 759-65 31-2 98-018 764-54 31-3 98-332 769-45 31-4 98-646 774-37 31-5 98-960 779-31 31-6 99-274 784-27 31-7 99-588 789-24 31-8 99-903 794-23 31-9 100-22 799-23 32-0 100-53 804-25 32-1 100-85 809-28 32-2 101-16 814-33 32-3 101-47 819-40 32-4 101-79 824-49 32-5 102-10 829-58 32-6 102-42 834-69 32-7 102-73 839-82 32-8 103-04 844-96 32-9 103-36 850-12 33 '0 103-67 855-30 33-1 103-99 860-49 33-2 104-30 865-70 33-3 104-62 870-92 33-4 104-93 876-19 33-5 105-24 881-41 33-6 105-56 886-68 33-7 105-87 891-97 33-8 106-19 897-27 33-9 106-50 902-59 34-0 106-81 907-92 34-1 107-13 913-27 34-2 107-44' 918-63 34-3 107-76 924-01 34-4 108-07 929-41 34-5 108-38 934-82 34-6 108-70 940-25 34-7 109-01 945-69 961 -00 967-21 973-44 979-69 985-96 992-25 998-56 1004-89 1011-24 1017-61 1024-00 1030-41 1036-84 1043-29 1049-76 1056-25 1062-76 1069-29 1075-84 1082-41 1089-00 1095-61 1102-24 1108-89 1115-56 1122-25 1128-96 1135-69 1142-44 1149-21 1156-00 1162-81 1169-64 1176-49 1183-36 1190-25 1197-16 1204-09 29791-000 30080-231 30371-328 30664-297 30959-144 31255-875 31554-496 31855-013 32157-432 32461-759 32768-000 33076-161 33386-248 33698-267 34012-224 34328-125 34645-976 34965-783 35287-552 35611-289 35937-000 36264-691 36594-368 36925-037 37259-704 37595-375 37933-056 38272-753 38614-472 38958-219 39304-000 39651-821 40001 -688 40353-607 40707-584 41063-525 41421-736 41781-923 v« IF 5-5678 3-1414 5-6767 3-1448 5-5857 3-1481 5-5946 3-1515 6-6036 3-1649 6-6124 3-1682 5-6213 3-1616 5-6302 3-1648 5-6391 3-1681 5-6480 3-1716 5-6569 3-1748 6-6656 3-1781 6-6745 3-1814 5-6833 3-1847 6-6921 3-1880 5-7008 3-1913 5-7066 3-1946 6-7183 3-1978 5-7271 3-2010 6-7358 3-2043 5-7447 3-2075 6-7532 3-2108 5-7619 3-2140 6-7706 3-2172 5-7792 3-2204 6-7879 3-2237 6-7966 3-2269 6-8051 3-2301 5-8137 3-2332 5-8223 3-2364 5-8310 3-2396 5-8396 3-2424 6-8480 3-2460 5-8566 3-2491 5-8761 3-2522 5-8736 3-2554 5-8821 3-2586 6-8906 3-2617 72 THE TECHNICAL CHEMISTS' HANDBOOK TABLE M— Continued. n O «2 • «2 n» iJn :/» 34-8 109-33 951-15 1211-04 42144-192 5-8991 3-2648 34-9 109-64 956-62 1218-01 42508-649 5-9076 3-2679 35-0 109-96 962-11 1225-00 42875-000 5-9161 3-2710 35-1 110-27 967-62 1232-01 43243-551 6-9245 3-2742 35-2 110-58 973-14 1239-04 43614-208 5-9326 3-2773 35-3 110-90 978-68 1246-09 43986-977 5-9413 3-2804 35-4 111-21 984-23 1253-16 44361-864 6-9497 3-2836 35-5 111-53 989-80 1260-25 44738-875 5-9681 3-2866 35-6 111-84 995-38 1267-36 45118-016 5-9665 3-2897 35-7 112-15 1000-98 1274-49 45499-293 5-9749 3-2927 35-8 112-47 1006-60 1281-64 45882-712 5-9833 3-2958 35-9 112-78 1012-23 1288-81 46268-279 6-9916 3-2989 3B-0 113-10 1017-88 1296-00 46656-000 6-0000 3-3019 36-1 113-41 1023-54 1303-21 47045-881 6-0083 3-3050 36-2 113-73 1029-22. 1310-44 ■47437-928 6-0166 3-3080 36-3 114-04 1034-91 1317-69 47832-147 6-0249 3-3111 36-4 114-35 1040-62 1324-96 48228-544 6 0332 3-3141 36-5 114-67 1046-35 1332-25 48627-125 6 0415 3-3171 36-6 114-98 1052-09 1339-56 49017-896 6-0497 3-3202 36-7 115-30 1057-84 1346-89 49430-863 6-0680 3-3232 36-8 115-61 1063-62 1354-24 49836-032 6-0663 3-3262 36-9 115-92 1069-41 1361-61 50243-409 6 0745 3-3292 37-0 116-24 1075 -21 ■ 1369-00 50653 000 6-0827 3-3322 37-1 116-65 1081-03 1376-41 51064-811 6-0909 3-3352 37-2 116-87 1086-87 1383-84 51478-848 6-0991 3-3382 37-3 117-18 1092-72 1391-29 51895-117 6-1073 3-3412 37-4 117-50 1098-58 1398-76 52313-624 61155 3-3442 37-5 117-81 1104-47 1406-25 52734-375 6-1237 3-3472 37-6 118-12 1110-36 1413-76 53157-376 6-1318 3-3601 37-7 118-44 1116-28 1421-29 53582-633 6-1400 3-3631 37-8 118-75 1122-21 1428 -84 54010152 6-1481 3-3561 37-9 119-07 1128-15 1436-41 54439-939 6-1563 3-3690 38-0 119-38 1134-11 1444-00 54872-000 6-1644 3-3620 38-1 119-69 1140-09 1451-61 55306-341 6-1726 3-3649 38-2 120-01 1146-08 1459-24 55742-968 61806 3-3679 38-3 120-32 1152-U9 1466-89 56181-887 6-1887 3-3708 38-4 120-64 1168-12 1474-66 96623-104 6-1967 3-3737 MATHEMATICAL TABLES TABLE SA—Cmtimted. 73 n O • rfi J.3 \ln V^ 38-5 120-95 1164-16 1482-25 57066-625 6-2048 3-3767 38-6 121-27 1170-21 1489-96 57512-466 6-2129 3-3797 38-7 121-58 1176-28 1497-69 67960-603 6-2209 3-3825 38-8 121-80 1182-37 1505-44 68411-072 6-2289 3-3854 38-9 122-21 1188-47 1613-21 58863-869 6-2370 3-3883 39-0 122-52 1194-59 1621-00 59319-000 6-2450 3-3912 39-1 122-84 1200-7'2- 1528-81 69776-471 6-2530 3-3941 39-2 123-15 1206-87 1536-64 60236-288 6-2610 3-3970 39-3 123-46 1213-04 1544-49 60698-467 6-2689 3-3999 39-4 123-78 1219-22 1662-36 61162-984 6-2769 3-4028 39*5 124-09 1225-42 1560-25 61629-875 6-2849 3-4066 39-6 124-41 1231-63 1568-16 62099-136 6-2928 3-4085 39-7 124-72 1237-86 1576-09 62570-773 6-3008 3-4114 39-8 125-04 1244-10 1684-04 63044-792 6-3087 3-4142 39-9 125-35 1250-36 1692-01 63521-199 6-3166 8-4171 40-0 125-66 1256-64 1600-00 64000-000 6-3245 3-4200 40-1 125-98 1262-93 1608-01 64481-201 6-3325 3-4228 40-2 126-29 1269-23 1616-04 64964-808 6-3404 3-4266 40-3 126-61 1275-56 1624-09 65450-827 6-3482 3-4285 40-4 126-92 1281-90 1632-16 65939-264 6-3561 3-4313 40-5 127-23 1288-25 1640-25 66430-126 6-3639 3-4341 40-6 127-55 1294-62 1648-36 66923-416 6-3718 3-4370 . 40-7 127-86 1301-00 1656-49 67419-143 6-3796 3-4398 40-8 128-18 1307-41 1664-64 67917-312 6-3875 3-4426 40-9 128-49 1313-82 1672-81 68417-929 6-3953 3-4464 41-0 128-81 1320-25 1681-00 68921-000 6-4031 3-4482 41-1 129-12 1326-70 1689-21 69426-631 6-4109 3-4510 41-2 129-43 1333-17 1697-44 69934-528 6-4187 3-4638 41-3 129-75 1339-65 1705-69 70444-997 6-4265 3-4666 41-4 130-06 1346-14 1713-96 70967-944 6-4343 3-4594 41-5 130-38 1352-65 1722-25 71473-375 6-4421 3-4622 41-6 130-69 1359-18 1730-56 71991-296 6-4498 3-4650 41-7 131-00 1365-72 1738-89 72511-719 6-4575 3-4677 41-8 131-32 1372-28 1747-24 73034-632 6-4653 3-4705 41-9 131-63 1378-85 1755-61 73660-059 6-4730 3-4733 42-0 131-95 1385-44 1764-00 74088-000 6-4807 3-4760 42 •! 132-26 1392-05 1772-41 74618-461 6-4884 3-4788 42-2 132-58 1398-67 1780-84 75151-448 6 4961 3-4815 74 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 3i— Continued. n Trn O "4- • n" «» n/» l/» 42-3 132-89 1405-31 1789-29 75686-967 6-5038 3-4843 42-4 133-20 1411-96 1797-76 76225-024 6-5115 3-4870 42-5 133-52 1418-63 1806-25 76765-625 6-5192 3-4898 42-6 133-83 1425-31 1814-76 77308-776 6-5268 3-4925 42-7 134-15 1432-01 1823-29 77854-483 6-5345 3-4952 42-8 134-46 1438-72 1831-84 78402-752 6-5422 3-4980 42-9 134-77 1445-45 1840-41 78953-589 6-5498 3-5007 43-0 135-09 1452-20 1849-00 79507-000 6-5574 3-5034 43-1 135-40 1458-96 1857-61 80062-991 6-5651 3-5061 43-2 135-72 1465-74 1866-24 80621-568 6-5727 3-5088 43-3 136-03 1472-54 1874-89 81182-737 6-5803 3-5115 43-4 136-35 1479-34 1883-56 81746-504 6-5879 3-5142 43-6 136-66 1486-17 1892-25 82312-87S 6-5954 3-5169 43-6 136-97 1493-01 1900-98 82881-856 6-6030 3-5196 43-7 137-29 1499-87 1909-69 83453-453 6-6106 3-5223 43-8 137-60 1506-74 1918-44 84027-672 6-6182 3-5250 43-9 137-92 1513-63 1927-21 84604-519 6-6257 3-5277 44-0 138-23 1520-53 1936-00 85184-000 6-6333 3-5303 44-1 138-54 1527-45 1944-81 85766-121 6-6408 3-5330 44-2 138-86 1534-39 1953-64 86350-888 6-6483 3-5357 44-3 139-17 1541-34 1962-49 86938-307 6-6558 3-5384 44-4 139-49 1548-30 1971-36 87628-384 6-6633 3-5410 44-5 139-80 1555-28 1980-25 88121 -125 6-6708 3-5437 44-6 140-12 1562-28 1989-16 88716-536 6-6783 3-5463 44-7 140-43 1569-30 1998-09 89314-623 6-6858 3-5490 44-8 140-74 1576-33 2007-04 89915-392 6-6933 3-5516 44-9 141-06 1583-37 2016 01 90518-849 6-7007 3-5543 45-0 141-37 1590-43 2025-00 91125-000 6-7082 3-5569 45-1 141-69 1597-51 2034-01 91733-851 6-7156 3-5595 45-2 142-00 1604-60 2043-04 92345-408 6-7231 3-5621 45-3 142-31 1611-71 2052-09 92959-677 6-7305 3-5648 45-4 142-63 1618-83 2061-16 93576-664 6-7379 3-5674 45-5 142-94 1625-97 2070-25 94196-375 6-7454 3-5700 45-6 143-26 1633-13 2079-36 94818-816 6-7528 3-5726 45-7 143-57 1640-30 2088-49 95443-993 6-7602 3-5752 45-8 143-88 1647-48 2097-64 96071-912 6-7676 3-5778 45-9 144-20 1654-68 2106-81 96702-579 6-7749 3-5805 MATHEMATICAL TABLES TABLE Zi—Gontvrmed. 75 n irn O 4 • n^ «= \Jn :/» 46-0 144-51 1661-90 2116-00 97336-000 6-7823 3-5830 46-1 144,-83 1669-14 2125-21 97972-181 6-7897 3-5856 46-2 145-14 1676-39 2134-44 98611-128 6-7971 3-5882 46-3 145-46 1683-65 2143-69 99252-847 6-8044 3-5908 46-4 145-77 1690-93 2152-96 99897-344 6-8117 3-5934 46-5 146-08 1698-23 2162-25 100544-625 6-8191 3-5960 46-6 146-40 1705-54 2171-56 101194-696 6-8264 3-6986 46-7 146-71 1712-87 2180-89 101847-563 6-8337 3-6011 46-8 147-03 1720-21 2190-24 102503-232 6-8410 3-6037 46-9 147-34 1727-57 2199-61 103161-709 6-8484 3-6063 47-0 147-65 1734-94 2209-00 103823-000 6-8556 3-6088 47-1 147-97 1742-34 2218-41 104487-111 6-8629 3-6114 47-2 148-28 1749-74 2227-84 105154-048 6-8702 3-6139 47-3 148-60 1757-16 2237-29 105823-817 6-8775 3-6165 47-4 148-91 1764-60 2246-76 106496-424 6-8847 3-6190 47-5 149-23 1772-05 2256-25 107171-875 6-8920 3-6216 47-6 149-54 1779-52 2265-76 107850-176 6-8993 3-6241 47-7 149-85 1787-01 2275-29 108531 -333 6-9065 3-6267 47-8 150-17 1794-51 2284-84 109215-352 6-9137 3-6292 47-9 150-48 1802-03 2294-41 109902-239 6-9209 3-6317 48-0 150-80 1809-56 2304-00 110592-000 6-9282 3-6342 48-1 151-11 1817-11 2313-61 111284-641 6-9354 3-6368 48-2 151-42 1824-67 2323-24 111980-168 6-9426 3-6393 48-3 151-74 1832-25 2332-89 112678-587 6-9498 3-6418 48-4 152-05 1839-84 2342-56 113379-904 6-9570 3-6443 48-5 152-37 1847-45 2352-25 114084-125 6-9642 3-6468 48-6 152-68 1855-08 2361-96 114791-256 6-9714 3-6493 48-7 153-00 1862-72 2371-69 115501-303 6-9785 3-6518 48-8 153-31 1870-38 2381-44 116214-272 6-9857 3-6543 48-9 153-62 1878-05 2391-21 116930-169 6-9928 3-6568 , 49-0 153-94 1885-74 2401-00 117649-000 7-0000 3-6593 49-1 154-25 1893-45 2410-81 118370-771 7-0071 3-6618 49-2 154-57 1901-17 2420-64 119095-488 7-0143 3-6643 49-3 154-88 1908-90 2430-49 119823-157 7-0214 3-6668 49-4 155-19 1916-65 2440-36 120553-784 7-0285 3-6692 49 '5 155-51 1924-42 2450-25 121287-375 7-0356 3-6717 49-6 155-82 1932-21 2460-16 122023-936 7-0427 3-6742 49-7 156-14 1940-00 2470-09 122763-473 7-0498 3-6767 76 THE TECHNICAL CHEMISTS' HANDBOOK TABLE Zi— Continued. n Trn O »2 TT 4 • n^ n' Vn ^» 49-8 156-45 1947-82 2480-04 123505-992 7-0569 3-6791 49-9 156'77 1955-65 2490-01 124251-499 7-0640 3-6816 50-0 157-08 1963-50 2600-00 125000-000 7-0711 3-6840 51-0 160-22 2042-82 2601-00 132651-000 7-1414 3-7084 52-0 163-36 2123-72 2704-00 140608-000 7-2111 3-7325 53-0 166-50 2206-19 2809-00 148877-000 7-2801 3-7563 54-0 169-64 2290-22 2916-00 157464-000 7-3485 3-7798 65-0 172-78 2375-83 3025-00 166375-000 7-4162 3-8030 56-0 175-93 2463-01 3136-00 175616-000 7-4833 3-8259 57-0 179-07 2551-76 3249-00 185193-000 7-5498 3-8485 58-0 182-21 2642-08 3364-00 195112-000 7-6158 3-8709 59-0 185-35 2733-97 3481-00 205379-000 7-6811 3-8930 60-0 188-49 2827-44 3600-00 216000-000 7-7460 3-9149 61-0 191-63 2922-47 3721 -00 226981-000 7-8102 3-9365 62-0 194-77 3019-07 3844-00 238328-000 7-8740 3-9579 63-0 197-92 3117-25 3969-00 250047-000 7-9373 3-9791 64-0 201-06 3216-99 4096-00 262144-000 8-0000 4-0000 65-0 204-20 3318-31 4225-00 274625-000 8-0623 4-0207 66-0 207-34 3421-20 4356-00 287496-000 8-1240 4-0412 67-0 210-48 3525-66 4489-00 300763-000 8-1854 4-0615 68-0 213-63 3631-69 4624-00 314432-000 8-2462 4-0817 690 216-77 3739-29 4761-00 328509-000 8-3066 4-1016 70-0 219-91 3848-46 4900-00 343000-000 8-3666 4-1213 71-0 223-05 3959-20 5041-00 357911-000 8-4261 4-1408 72-0 226-19 4071-51 5184-00 373248-000 8-4853 4-1602 73-0 229-33 4185-39 5329-00 389017-000 8-5440 4-1793 74-0 232-47 4300-85 5476-00 406224-000 8-6023 4-1983 75-0 235-62 4417-87 5625-00 421875-000 8-6603 4-2172 76-0 238-76 4536-47 5776-00 438976-000 8-7178 4-2358 77-0 241-90 4656-83 5929-00 456533-000 8-7750 4-2643 78-0 245-04 4778-37 6084-00 474552-000 8-8318 4-2727 79-0 248-18 4901-68 6241-00 493039-000 8-8882 4-2908 80-0 251-32 5026-56 6400-00 512000-000 8-9443 4-3089 81-0 254-47 5153-01 6561-00 531441-000 9-0000 4-3267 82-0 257-61 5281-03 6724-00 551368-000 9-0654 4-3445 83-0 260-75 5410-62 6889-00 571787-000 9-1104 4-3621 84-0 263-89 5541-78 7056-00 592704-000 9-1652 4-3795 AREAS AND SOLID CONTENTS TABLE Zi— Continued. 77 n tttc o m2 7r — . 4 • tfi »3 vm l/» 85-0 267-03 5674-50 7225-00 614125-000 9-2195 4-3968 86-0 270-17 5808-81 7396-00 636056-000 9-2736 4-4140 87-0 273-32 5944-69 7569-00 658503-000 9-3274 4-4310 88-0 276-46 6082-13 7744-00 681472-000 9-3808 4-4480 89-0 279-60 6221-13 7921-00 704969-000 9-4330 4-4647 90-0 282-74 6361-74 8100-00 729000-000 9-4868 4-4814 91-0 285-88 6503-89 8281-00 753571-000 9-5394 4-4979 92-0 289-02 6647-62 8464-00 778688-000 9-5917 4-5144 93-0 292-17 6792-92 8649-00 804357-000 9-6437 4-5307 94-0 295-31 6939-78 8836-00 830584-000 9-6954 4-6468 95-0 298-45 7088-23 9025-00 857375-000 9-7468 4-5629 96-0 301-59 7238-24 9216-00 884736-000 9-7980 4-5789 97-0 304-73 7389-83 9409-00 912673-000 9-8489 4-5947 98-0 307-87 7542-98 9604-00 941192-000 9-8995 4-6104 99-0 311-02 7697-68 9801-00 970299-000 9-9499 4-6261 100-0 314-16 7854-00 100000-00 1000000-000 10-0000 4-6416 Approximately ^0^+6 = + 5- and ^a^±6 = 0+3-2 TABLE 35.— POBMULiE FOR MENSURATION OP AREAS AND SOLID CONTENTS. 1. — Triangle. Area = -5- x base x height. If all the sides, a, b, c, are known and half their sum Is represented u 1.1. 1. a + h + c ,, by s, so that s = — - — then A= n/s(«-o)(s-6)(s-c) 2.— Circle. Area of circle, if 4=dlameter, r=radius, and Tr=3-14159 A =^i» = j-V . . ■ (j = 0-7854^ d = 1-12838 n/X 78 THE TECHNICAL CHEMISTS' HANDBOOK Area of segment of circle of an arc of a" Or, if ci is the diameter and h the height of segment, calculate -J- and find the value x, in the following table, corresponding to -J- ; the square of the diameter multiplied by as, gives the area of the segment. Area of segment = x6P. h h a h d X d X d X d X •01 •00133 •14 •06683 •27 •17109 •40 •29337 ■02 •00375 •15 •07387 •28 •18002 •41 •30319 •03 •00687 •16 •08111 •29 •18905 •42 •31304 •04 •01054 •17 •08854 •30 •19817 •43 •32293 ■05 •01468 •18 •09613 •31 •20737 •44 •33284 •06 •01924 •19 •10390 •32 •21667 •45 ■34278 •07 ■02417 •20 •11182 •33 •22603 •46 ■35274 ■08 •02944 . •21 •11990 •34 ■23547 •47 ■36272 ■09 ■03501 •22 •12811 •35 •24498 •48 ■37270- •10 •04087 •23 •13646 •36 •25455 •49 •38270 •11 •04701 •24 •14495 •37 •26418 •50 •39270 ■12 ■05338 •25 •15355 •38 ■27386 •13 •06000 •26 •16226 •39 •28369 S. — Cone and Pyramid. Solid content : S = — base x height, o A rea o f convex surface of right cone : When s = side of cone = iJi^ X A^ where r = radius of base and h = height of cone, the area of convex surface will be A = Trrs. Area of convex surface Content of cylinder -Cylinder. = 27rrft. : base X height. Convex surface Surface of segment 5.- A = A = -Sphere. 47rr'=12^56636r2. 2Trh, h = height of segment. Sohd content of sphere S = ,-j'3jr = 4-1888}-'. WEIGHTS AND MEASURES 79 Solid content of sphere S = -vd' = 0-5236dK Radius r = 0-62035 ^content. Content of segment of sphere : If a is the radius of the sectional area, h the height of the segment, and r the radius of the sphere, = lTh\Zr-h). Solid content of spherical zone : If a and 6 are the respective radii of the two terminal surfaces, and h the height, S = i7rA(3a2 + 36^ + ^2). TABLE 36.— WEIGHTS AND MEASURES OP DIFFERENT COUNTRIES. 1. Metric System (compulsory in France, Germany, Austria, the Netherlands, Belgium, Luxemburg, Switzerland, Italy, Greece, Turkey, Roumania, Spain, Portugal, and most of the South American Republics ; optional in Great Britain, the United States, and Russia). 1 metre (m.) = 443 '296 Paris lignes = 3-280899 English feet=3-18620 Prussian feet=l •00000301 mtoes des archives. 1 kilometre (km.) = 10 hectometres (hm.) = 0-6214 English mile = 0-1328 Prussian mile-0-9375 Russian verst= 0-5390 nautical mile = 0-1347 geographical mile (15 to 1 degree of longitude). 1 lieue (France) = 1 myriametre=10 km. 1 German mile = 7J km. =0-996 Prussian mile=4-66 English miles. 1 hectare (ha.) = 100 ares (a.) = 10,000 sq.m. = 0-01 sq.km.=2-471 English acres. 1 litre (l.) = 0-001 cb.m. =1000 c.cm. =0-2201 gallon. 1 hectolitre (hl.) = 0-l cb.m. =100 1. =22-01 gallons. 1 kilogram (kg.)=1000 g.^weight of 1 litre of water at +4° C. =2 German and Swiss pounds (zollpfund) = -999999842 kilogram prototype = 2-2046 pounds avoirdupois = 1-7857 Austrian pounds = 2-3511 Swedish pounds=2-4419 Russian pounds. 1 gram (g.)=15-432 grains (English). 1 quintal=100 kg.=196-84 lbs. avoirdupois = 1 cwt. 3 qrs. 0-84 lb. 1 metrical ton = 1000 kg. =0-9842 English ton = 1-023 American short tons (at 2000 lbs.). 80 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 36— Continued. 2. Oreat Britain and Ireland. 1 foot=0-3047943 m. 1 inch = 25 -3995 mm. 1 yard = 3 feet=0-9143835 m. 1 fathom = 2 yards = 1-829 m. 1 rod (pole, perch) = 5J yards = 5 '029109 m. 1 statute mile = 8 furlongs = 320 poles = 1760 yards = 6280 feet = 1-6093 kilometre (km.). 1 nautical mile=YVth degree (at the equator). 6082-66 feet=1854-96m. 1 acre = 4 roods = 160 poles = 0-40467 ha. =43560 square feet = 4047 square metres. 1 square mile = 640 acres = 258 -989 ha. 1 gallon = 4 quarts = 8 pints = 277 -274 cubic inches = 4 -536 litres. 1 cubic foot=l728 cubic inches = 28-3153 1. 1 cubic inch = 16-3862 c.cm. 1 quarter=8 bushels = 32 pecks = 64 gallons = 2 -903 hi. 1 bushel = 8 gallons = 0-3628 hi. 1 fluid ounce = ^th pint = 28 -35 c.cm. 1 pound avoirdupois (lb.) = 16 ounces (oz. )= 7000 grains = -4635926 kg. 1 ounce avoirdupois = 437^ grains = 28 -35 g. 1 gallon = 10 lbs. water = 70,000 grains = 4-535926 kg. water. 1 hundredweight (cwt.) = 4 quarters (qr.)=8 stones = 112 lbs. = .')0-8024kg. 1 ton = 20 cwt.=2240 lbs. = 1016-648 kg. Apothecaries' Weight. 1 pound troy = 12 ounces troy=96 drams = 288 scruples = 5760 grains = 373 -24195 g. 1 ounce troy = 8 drams = 24 scruples = 480 grains = 31 -1035 g. 1 ounce troy (for gold and precious stones)=20 pennyweight (dwt.) = 480 grains = 31 -1035 g. 1 pennyweight (dwt. ) = 1 -552 g. 1 grain (common to avoirdupois and troy weight) = 0-06479895 g. 3. Austria (old measures and weights, now abolished for the metric system). 1 foot=0-316102 m., at 12 inches of 12 lines each. 3 ruthen = 5 klafter = 30 feet = 360 zoU. 1 meile=4000 klafter=7586-455 m. 1 maass = 1-415 1. 1 eimer = 40 maass = 160 seidel. 1 metze = 6r4995 1. 1 Wiener pfund = 560-012 g. 1 centner=5 stein = 100 pfund = 3200 loth. 4. Denmark and Nor-way employ, as unit of measure, the Prussian foot, as unit of weight the units of the metrical system, viz., kilos, etc. WEIGHTS AND MEASURES 81 TABLE BG—Oontinued. 6. Prussia (old system, now abolished for the metric system). 1 foot (Rhenish foot)=12 zoU (inches)=144 llnien = 0-313863 m. 1 ruthe = 12 fuss = 3 -76624 m. 1 lachter (fathom) = 80 zoll = 2-09326 m. 1 meile = 24,000 fuss = 7532-5 m. 1 morgeD = 180 square ruthen = 0'2553 ha. 1 quart=64 cubic inches=^V cubic foot=l'14503 1. 1 scheffel = 16 Metzen = 48 quarts = 0-64961 hi. 1 tonne =4 scheffel=2-19846 hi. 1 klafter=108 cubic fuss = 3 -3389 cb.m. 1 schachtruthe = 144 cubic fuss = 4-4519 cb.m. 1 pfund=30 loth = 300 quentchen = 500 g. 1 centner=100 pfund=50 kg. (Formerly 1 pfund=32 loth = 467-711 g. ; 1 centner=110 pfund.) 6. Russia. lfoot=l English foot. lsashehn = 7 feet=3 arshin = 12 tchetvert = 48 vershok=2-13357 m. 1 verst= 500 sashehn = 1066-78 m. 1 dessatine=2400 square sashehns = 10925 m. 1 vedro = 10 krushky (stoof}= 12-299 1. 1 tchetvert=l osmini = 4 payok = 8 tchetverlk=209'9 1. 1 pound = 32 loth = 96 solotmk=9216 doli = 0-9028 Eng. lb. = 409-531 g. 1 berkovets = 10 pud=400 pounds = 163-81 kg. 1 pud=40 pounds = 36-112 Eng. lb. = 16-3805 kg. 7. Siweden. 1 foot=10 zoU (inches) = 100 lines =;0-97408 Eng. foot = 0-296901 m. 1 famn (fathom) = 3 alnar (ells) = 6 feet=5-58445 Eng. feet = 1-7814 m. 1 mile = 6000 fathoms = 6-6417 Eng. statute niiles = 10-6884 km. 1 kanne = 100 cubic inches = 0-57694 Eng. gallon = 2-617 1. 1 skalpund=100 korn (at 100 art) = 0-9378 Eng. lb. = 425-3395 g. 1 centner = 100 skalpund. 1 skipspund = 20 liespund = 400 skalpund. 8. Switzerland. Metrical measure and weight. The following are sometimes still employed : — 1 fuss = 0-3000 m. = 0-9843 Eng. foot. 1 juchart = 36 are = 0-88956 Eng. acre. 1 maass = l-51 1. 1 saum = 100 maass = 151 1. 9. United States. Weights and measures as in Great Britain, but instead of the " long ton " (gross ton) of 2240 lbs., more frequently the "short ton ' (net ton) of 2000 lbs. = 907-1852 kg. = 0-89285 long ton, is employed. The U.S. gallon differs from the British gallon; it is = 3'7854 litres. For timber, the measure is the " cord " = 4x4x8 feet = 128 cubic feet=about 2i cubic metres. F 82 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 36— Continued. 10. South America (Bolivia, Chile, Colombia, Ecuador, Guatemala, Honduras, Nicaragua, Peru, San Salvador, Venezuela) — 1 quintal =46 -0093 kg. Argentina. . . 1 quintal =45 -9367 kg. Brazil . . . 1 „ =58-752 „ Paraguay . . . 1 „ =46-008 „ Uruguay . . . 1 ,, =45-94 „ Square Feet, Square Metre. 1 square metre (sq.m.) = 10-764 square feet (English and Russian) = 10-008 square feet (Austrian)= 10-152 square feet (Prussian and Danish) = 11 -344 square feet (Swedish). 1 square foot (English and Russian)= 0-09290 square metre. Cubic Feet, Cubic Metre. 1 cubic metre (cb.m.)= 35-316 cubic feet (English and Russian). 1 ,, „ =31-66 „ (Austrian). 1 ,, „ =32-346 „ (Prussian and Danish). 1 „ „ =38-209 „ (Swedish). 1 cubic foot (English and Russian) = 0-028315 cubic metre. 1 Kilogram per Running Metre = 0-6719 English pound per running foot. = 0-6277 zollpfund per Prussian foot. 1 English pound per 1 English foot =1-4882 kg. per running metre. 1 Kilogram per Square Centimetre (for steam pressure) = 14-223 English pounds per square inch. = 13-631 zollpfund per Prussian square inch. = 13-878 zollpfund per Austrian square inch. HORSB-PO'WBR (per second). Kg.-m. Austria. Foot-pounds. Prussia. Foot-pounds. England. Foot-pounds. Sweden. Foot-pounds. Russia. Foot-pounds. 75 76-041 474-53 481-11 477-93 484-56 542-47 550 593-90 602-14 600-85 609-19 75 kilogram-metres taken as unit, 550 English foot-pounds taken as unit, = 1 Admiralty horse-power per second ; or, 33,000 foot-pounds per minute. WEIGHTS AND MEASURES 83 TABLE 37.— TABLES FOR REDUCING ENGLISH TO METRICAL WEIGHTS AND MEASURES, AND VICE VERSA. Reduction of Metrical Measure to Engiisli Measure. Metre. Sq.m. Cub.m. ' Feet. Inclies. Square feet. Square inches. Cubio feet. Cubio inches. 1 3-2809 39-3706 10-7642 1550-05 35-3161 61026-2 2 6-5618 78-7412 21-5284 3100-09 70-6322 122052-4 3 9-8427 118-1118 32-2926 4650-13 105-9483 183078-6 4 13-1235 157-4824 43-0568 6200-18 141-2644 244104-9 5 16-4044 196-8530 53-8210 7750-23 176-5805 305131-1 6 19-6853 236-2237 64-5852 9300-27 211-8966 366157-3 7 22-9662 275-5943 75-3494 10860-31 247-2126 427183-5 8 26-2471 314-9649 86-1136 12400-36 282-5287 488209-7 9 29-5280 354-3355 96-8778 13950-40 317-8448 649235-9 Bnglisli Feet = Metres. Ft. 0. 1. 2. 3. i. 6. 6. 7. 8. 9. 0-0000 3048 0-6096 0-9144 1-2192 1-5240 1-8288 2-1886 2-4384 2-7432 10 3-0479 8-3527 3-6575 3-9623 4-2671 4-6719 4-8767 5-1815 5-4863 5-7911 20 6-0969 6-4007 6-7065 7-0108 7-8161 7-6199 7-9247 8-2295 8-5342 8-8890 SO 9-1488 9-4486 0-7634 10-068 10-863 10-668 10-973 11-277 11-582 11-887 40 12-192 12-497 12-801 13-106 13-411 18-716 14-021 14-826 14-680 14-936 50 16-240 15-646 15-849 16-164 16-459 16-764 17-068 17-873 17-678 17-983 60 18-288 18-592 18-897 19-202 19-507 19-812 20-116 20-421 20-726 21-081 70 21-336 21-640 21-946 22-250 22-556 22-860 23-164 28-469 23-774 24-079 80 24-384 24-688 24-993 25-298 25-603 25-908 26-211 26-517 26-882 27-127 90 27-432 27-786 28-041 28-346 28-651 28-966 29-260 29-565 29-870 30-175 100 80-479 80-784 31-089 31-394 31-699 82-003 82-808 32-618 82-918 83-223 110 83-627 38-832 34-187 34-442 34-747 36-061 36-866 85-661 36-966 36-271 120 36-676 36-880 87-186 37-490 87-795 88-099 38-404 38-709 89-014 89-818 130 39-623 89-928 40-233 40-538 40-842 41-147 41-462 41-757 42-062 42-366 140 42-671 42-976 48-281 48-586 48-890 44-196 44-600 44-806 45-110 45-414 160 46-719 40-024 46-320 46-634 46-938 47-243 47-548 47-858 48-168 48-462 160 48-767 49-072 49-877 49-642 49-986 50-291 60-696 60-901 61-206 51-610 iro 61-816 62-120 52-426 52-729 63-084 68-839 63-664 63-943 54-268 54-668 180 54-863 66-168 65-473 65-777 66-082 66-887 56-692 66-997 67-301 67-606 190 57-911 58-216 68-521 68-826 69-130 69-435 69-740 60-046 60-349 60-664 84 THE TECHNICAL CHEMISTS' HANDBOOK English Inches = Millimetres. Inch. MiUimotres. iDchea. Millimetres. Inches. Millimetres. A 0-39 1 25-4 7 177-8 w 0-79 2 50-8 8 203-2 ^ 1-59 3 76-2 9 228-6 i 3-17 4 101-6 10 254-0 i 6-35 5 127-0 11 279-4 4 12-70 6 162-4 12 304-8 Snglish Square Feet = Square Metres. Sq.ft. 0. 1. 2. 3. 4. 6. 6. 7. 8. 9. 0-0000 0-0929 01868 0-2787 0-3716 0-4645 0-5574 0-6503 0-7432 0-8361 10 0-9290 1-0219 1-1148 1-2077 1-3006 1-3935 1-4864 1-6793 1-6722 1-7661 20 1-8580 1-9509 2-0438 2-1307 2-2296 2-3226 2-9164 2-6083 2-6012 2-6941 30 2-7870 2-8799 2-9728 3-0657 3-1586 3-2615 3-3444 3-4373 3-5302 3-6231 40 3-7160 3-8089 3-9018 3-9947 4-0876 4-1805 4-2734 4-3663 4-4592 4-6621 60 4-6460- 4-7379 4-8308 4-9237 5-0166 6-1095 6-2024 6-2953 6 -3882 6-4811 60 6 -5740 5-6669 6-7598 6-8627 5-9456 6-0386 6-1314 6-2243 6-3172 6-4101 70 6-6030 6-5959 6 6888 6-7817 6-8746 6-9676 7-0604 7-1533 7-2462 7-3391 80 7-4320 r-5249 7-6178 7-7107 7-8036 7-8966 7-9894 8-0823 8-1762 8-2681 90 8-3610 8-4539 8-5468 8-6397 8-7326 8-8265 8-9184 9-0113 9-1042 9-1971 Suglish Square laches =: Square Centimetres. Sij. ius. 0. 1. 2. 3. 4. 6. 6. 7. 8. 9. 0-0000 0-4514 12-903 19-354 25-806 32-257 38-708 45-160 61-611 68-062 10 64-614 70-965 77-416 83-868 90-319 96-771 103-22 109 67 116-12 122-58 20 129-03 135-48 141-93 148-38 164-88 161-28 167-74 174-19 180-64 187-09 30 193-64 199-99 206-44 212-90 219-36 226-80 232-25 238-70 246-16 261-60 40 268-05 264-61 270-96 277-41 283-86 290-31 296-76 303-21 309-67 316-12 60 322-67 329-02 335-47 341-92 348-37 354-83 361-28 367-78 374-18 380-63 60 337-08 393-63 399-98 406-44 412-89 419-34 426-79 432-24 438-69 446 14 •70 461-60 468-06 464-60 470-95 477-40 483-85 490-30 496-76 603-21 509-69 80 616-11 622-56 625-01 535-46 641-91 548-37 664-82 561-27 667-72 674-17 90 580-62 587-07 693-53 699-98 606-48 612-88 619-33 626-78 632-23 638-6p WEIGHTS AND MEASURES 85 English Cubic Feet = Cubic Metres. Cub. ft. 0. 1. 2. 3. 4. 6. 6. 7. 8. 9. 0-0000 0-0283 0-0666 0-0849 0-1133 0-1416 0-1699 0-19S2 0-2266 0-2548 10 0-2832 0-3116 0-3398 0-3681 0-3964 0-4247 0-4530 0-4814 0-5097 0-6380 20 0-6663 6-5946 0-6229 0-6513 0-6796 0-7079 0-7362 0-7646 0-7928 0-8311 30 0-8494 0-8778 0-9061 0-9344 0-9627 0-9910 1-0194 1-0477 1-0760 1-1043 40 1-1326 1-1609 1-1892 1-2176 1-2459 1-2742 1-3026 1-3308 1-3591 1-3875 60 1-4168 1-4441 1-4724 1-5007 1-6290 1-6573 1-6867 1-6140 1-6423 1-6706 60 1-69S9 1-7272 1-7655 1-7839 1-8122 1-8406 1-8688 1-8971 1-9264 1-9638 VQ 1-9821 2-0104 2-0387 2-0670 2-0953 2-1230 2-1620 2-1803 2-2086 2-2369 80 2-2652 2-2935 2-8219 2-3602 2-3785 2-4068 2-4351 2-4634 2-4917 2-5201 90 2-6484 2-6767 2-6050 2-6333 2-6616 2-6900 2-71S3 2-7466 2-7749 2-8032 English Cubic Inches = Cubic Centimetres. Cub. ill. 0. 1. 2. 3. 4. 6. 6. 7. 8. 9. o-oooo 16-386 32-772 49-159 66-646 81-931 98-317 114-70 131-09 147-48 10 163-86 180-25 196-63 213-02 229-41 246-79 262-18 278-56 294-95 311-34 20 327-72 344-11 360-50 376-88 393-27 409-65 426-04 442-43 458-81 476-20 30 491-59 507-97 524-36 540-74 557-18 673-62 689-90 606-29 622-67 639-06 40 655-46 671-83 688-22 704-61 720-99 737-38 753-76 770-15 786-64 802-92 60 819-31 835-69 852-08 868-47 884-86 901-24 917-63 934-01 950-40 966-78 60 933-17 999-56 1016-9 1032-3 1048-7 1066-1 1081-6 1097-9 1114-3 1130-6 70 1147-0 1163-4 1179-8 1196-2 1212-6 1229-0 1246-3 1261-7 1278-1 1294-6 80 1310-9 1327-3 1343-7 1360-1 1376-4 1392-8 1409-2 1462-6 1440-9 1468-4 90 1474-8 1491-1 1607-6 1523-9 1540-3 1566-7 1573-1 1589-6 1605-8 1622-2 English Pounds := Kilograms. Lbs. 0. 1. 2. 3. 4. 5. 6. 7. 8. 9. 0-0000 0-4586 0-9072 1-3608 1-8144 2-2680 2-7216 3-1761 3-6287 4-0823 10 4-6369 4-9896 6-4431 5-8967 6-3603 6-8039 7-2676 7-7111 8-1647 8-6188 20 9-0719 9-6254 9-9790 10-433 10-886 11-340 11-793 12-247 12-701 .^8-154 30 13-608 14-061 14-515 14-969 15-422 16-876 16-329 16-783 17-237 17-690 40 18144 18-597 19-061 19-604 19-958 20-412 29-866 21-319 21-772 22-226 60 22-680 23133 23-687 24-040 24-494 24-948 25-401 26-855 26 308 26-762 60 27-216 27-669 28-123 28-576 29-030 29-484 29-937 30-391 30-844 31-296 70 31-761 32-206 32-659 33-112 33-666 34-019 34-473 34-927 35-380 35-834 SO 36-287 30-741 37-196 37-648 38-102 38-555 39-009 39-463 39-916 40-370 90 40-823 41-277 41-731 42-184 42-638 43-091 43-545 43-998 44-452 44-906 86 THE TECHNICAL CHEMISTS' HANDBOOK Englisli Tons = Kilograms. 1 0. 1. 2. 3. 4. 5. 6. 7. 8. 9. 0-0000 1016 2032 3048 4064 6080 6096 7112 8129 9145 10 10161 11177 12193 13209 14225 15241 16257 17273 18289 19305 20 20321 2 1 337 22363 23369 24386 25402 26418 27434 28450 29466 30 30432 31498 32614 33530 34646 36562 36678 37694 38610 39627 40 40643 41659 42675 43691 44707 46723 46739 47765 48771 49787 60 50803 61819 62835 53851 64868 55884 66900 67916 68932 69948 60 60964 61980 62996 64012 65028 66044 67060 68076 69092 70108 70 71125 72141 73167 74173 76189 76205 77221 78237 79263 80269 80 81286 82302 83317 84333 85346 86366 87382 88398 89414 90430 90 91446 92246 98478 94494 96610 96626 97642 98568 99574 100590 English Grains = Grams. s ■g a 0. 1. 2. 3. 4. 6. 6. 7. 8. 9. ■065 -1296 ■194 -269 •324 •389 -454 -518 -683 10 ■648 -713 -778 -842 -907 972 1-037 1-102 1-166 1-231 20 1-296 1-361 1-426 1-490 1-555 1^620 1-685 1-749 1-814 1-879 30 1-944 2-009 2-074 2-138 2-203 2-268 2-333 2-397 2-462 2-627 40 2-692 2-667 2-721 2-786 2-861 2-916 2-981 3-045 3-110 3-175 60 3-240 3-306 3-369 3-434 3-499 3-564 3-629 3-693 3-768 3-823 60 3-888 3-963 4-018 4-082 4-147 4-212 4-277 4-341 4-406 4-471 70 4-636 4-601 4-666 4-730 4-795 4-860 4-926 4-989 6-054 5-119 80 6-184 8 249 5-314 6-378 6-443 6-608 6-673 5-637 5-702 6-767 90 6-832 6-897 5-962 6-026 6-091 6-166 6-221 6-286 6-360 6-415 Grams = English Grains. en a g 0. -1. -2. -3. -4. -5. ■6. -7. •8. -9. 1-643 8-036 4-629 6-172 7-716 9-26S 10-802 12-345 13-808 1 15-432 16-976 18-518 20-06] 21-604 23-148 24-691 26-234 27-777 29-320 2 30-864 32-407 33-960 35-493 37036 38-580 40-123 41-666 43-209 44-752 3 46-296 47-839 49-382 60-925 62-468 54012 55-555 57-098 58-641 60-184 4 61-728 63-271 64-814 66-375 67-900 69-444 70-987 72-630 74073 76-616 5 77-160 78-703 80-246 81-789 83-332 84-876 86-419 87-962 89-505 91-048 WEIGHT OF SHEET METALS 87 1 English pound (lb.) per sq. foot = 4*883 kg. persq. metre (sq.m.). 1 ,, ,, „ sq. inch = 0'07031 kg. per sq.m. 1 „ ton per sq. inch = 158 kg. per sq.cm. 1 „ pound per cub. foot = 16 "02 gm. per litre. 1 kilogram per sq. metre = 0'2048 lb. per sq. foot. 1 English grain per gallon = ■014286 gm. per litre. 1 ,, „ ,, English cub. foot = 2-287 gm. per cub. metre. 1 grm. per Utre = 70 grains per gallon = ■06243 lb. per cub. foot. 1 metre-kilogram (rakg.) = 7 -235 foot-pounds. 1 foot-pound = 0-1382 mkg. 1 foot-pound per cub. foot = 4-8807 mkg. per cub. met. TABLE 38.— WEIGHT OP SHEET METALS. Weight of a Superficial Foot. Thick, uess. ■Wrought Iron. Cast Iron. Steel. Copper. Brass. Lead. Zinc. Inch. Lb. Lb. Lb. Lb. Lb. Lb. Lb. A 2-53 2-34 2-55 2-89 2-73 3-71 2-34 i 5-05 4-69 5-10 5-78 5-47 7-42 4-69 A 7-58 7-03 7-66 8-67 8 20 11-13 7-03 i 10-10 9-38 10-21 11-76 10-94 14-83 9-38 A 12-63 11-72 12-76 14-45 13-67 18-54 11-72 i 15-16 14-06 15-31 17-34 16-41 22-25 14-06 A 17-68 16-41 17-87 20-28 19-14 25-96 16-41 i 20-21 18-75 20-42 23-13 21-88 29-67 18-75 ■A 22-73 21-09 22-97 26-02 24-61 33-38 21-09 § 25-27 23-44 25-52 28-91 27-34 37-08 23-44 H 27-79 25-78 28-07 31-80 30-08 40-79 25-78 i 30-31 • 28-13 30-63 34-69 32-81 44-50 28-13 if 32-84 30-47 33-18 37-58 35-55 48-21 30-47 i 35-87 32-81 35-73 40-47 38-28 51-92 32-81 H 37-90 35-16 38-28 43-36 41-02 55-63 35-16 1 40-42 37-50 40-83 46-25 43-75 59-33 37-50 88 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 39. -COINAGE OF DIFFERENT COUNTRIES. Exact Value in Austria — £ s. d. 1 Vereins Thaler (=1 former Prussian Thaler) . 2 11-24 1 Gulden = 100 Neukreuzer 1 11-49 1 Maria Theresia Thaler 4 1-46 1 Dukaten 9 4-78 4 Gulden Gold = 1 Francs ; 8 Gulden Gold - 20 Francs Belslum = France. Brazil — 1 Mareis = 1000 Reales ...... 2 3-48 Chili— 1 Peso = 100 Centavos 3 11-58 Denmark — 1 Rigsbankdaler=6 Marks = 90 Skillings . . 2 2-67 1 Krone = 100 Oere 1 0-83 Bast India — 1 Rupee = 16 Annas 14 Egypt — 1 Bag of Gold = 30,000 Piastres . . . . 273 2 10 1 Piastre = 40 Para 2-5 France — 1 Franc = 100 Centimes 9-516 The 20-Franc piece contains 5-8065 g. fine gold . 15 10-31 The 5-Franc piece contains 22-5 g. fme silver . 3 11 "58 German Empire — 1 Mark = 100 Pfennig 11-748 The 20 Mark piece contains 7-1685 g. fine gold . 19 6-96 The 5-Mark piece contains 25 g. fine silver . Great Britain — 1 Pound Sterling contains 7-3224 g. fine gold . 10 1 Shilling contains 5-231 g. fine silver ... 1 COINAGE OF DIFFERENT COUNTRIES 89 TABLE 39— Continued. Exact Value in Qreece — £ s. d. 1 Drachma =100 Lepta = l Franc ( = France). . 9-516 Italy— 1 Lira =1 Franc (= France) 9-516 Japan — 1 Gold Yen 4 1 Mezico — 1 Piastre (Peso, Mexican Dollar) = 8 Reales = 100 Cents 4 3-5 1 DobIon = 16 Piastres 3 8 8 Netherlands — 1 Guilder =100 Cents 18 1 WiUems d'Or 16 6-4 1 Ducat 9 4-5 Norivay — 1 Krone=100 Oere 1 0-83 1 Species Daler = 120 Skillings . . . . 4 5-43 Persia — 1 Toman =10 Keran 9 0-31 1 Rupee Silver 16-2 Peru — 1 Sol(Peso) = 10Dineros = 100Centavos . . 3 U-58 Portugal — 1 Milreis (in accounts) 4 6 -75 1 Milreis (silver) . 4 0-46 1 Tostao = 100Reis 4-8 Bonuiania — 1 Piastre = 1 Franc (France) 9-516 90 THE TECHNICAL CHEMISTS' HANDBOOK TABLE 39— Contimied. Russia — 1 Silver Rouble = 100 Kopeks .... 1 Half-Imperial = 5 Rouble Gold = 5 '9987 g. fine gold 1 Paper Rouble Servla — 1 Dinar =1 Franc ( = France) Spain— 1 Peseta=l Franc (=France) .... 1 Duro (Spanish Dollar) = 2 Escudos = 5 Pesetas Exact value iti £ s. d. 3 2-06 16 4-61 2 7-7 = 20 Reales 9-516 9-516 11-58 Sweden — 1 Kronor=100 Oere 0-83 Sivitzerland = France. Turkey — 1 Piastre = 40 Para =120 Asper 1 Turkish Pound (Yuslik) United States — 1 Dollar =10 Dimes = 100 Cents 1 Eagle = 10 DoUars = 15-0463 g. fine gold 18 2-1 1 1-15 1-16 SPECIAL PART FUEL AND FURNACES 93 I. FUEL AND FURNACES. A. — Fuel. Should be tested in the case of lignite, peat, coal, coke. Eefer to the Appendix as to sampling. 1. Moisture. — Heat 100 to 200 g. of coal to 110° (not above), for two hours, preventing access of air as much as possible. At a higher temperature the result might be too high, owing to escape of volatile matters, or too low, owing to a partial oxidation. The sample should be broken up quickly into pieces not smaller than a bean, otherwise too much water would evaporate during the process. Lignite and peat are heated to 100° for five or six hours, and repeatedly weighed, till no further diminution of weight takes place. Coke is heated to 110° for two hours. All other tests are made with air-dried material. The average sample is weighed before taking the samples for the tests ; it is then spread out in a thin layer and allowed to lie in ordinary dry air for forty-eight hours. It is then weighed again, and the results obtained with such air-dried fuel are calculated on the original (undried) material. 2. Residml Coke {Fixed Carbon). — One g. of finely powdered coal is placed in a platinum crucible at least Ij in. deep, weighing from 20 to 30 g., provided with a tightly fitting cover. The crucible should then be heated by means of an ordinary Bunsen burner, the flame of which should not be less than 7 in. high. The crucible should be supported on a triangle of thin platmum wire, and it should be so placed that the space between the bottom of the crucible and the top of the burner is 25 to 3 in. The heating ought not to last longer than a few minutes, but must be con- tinued as long as any appreciable quantity of inflammable matter escapes. The surface ot the crucible cover should then be clean, but its lower side should be covered with carbon. If the flame be smaller, or the crucible be supported by a stout wire triangle, the yield of coke will be too high. The results should always be calculated upon coal or coke free from ash, in order to render them comparative. Good coal for reverberatory furnaces should yield from 60 to 70 per cent, of coke. 3. Ash. — This estimation is very simple for lignite or peat ; coke requires a very high temperature ; coal which cakes presents most difficulties. The latter must be powdered very finely, and heated up gradually, so that the volatile matters may escape before the powder can form a cake. If an analysis is only occasionally required, 2 to 5 g. of finely ground coal is heated in a platinum crucible, which is fitted in a hole into a stoneware 94 THE TECHNICAL CHEMISTS' HANDBOOK slab, or, better, in asbestos board (Fig. 1). This is placed in a slanting position on a tripod stand. The slab serves to separate the air required for oxidation from the gases of the burner, and greatly hastens the combustion, which is thus completed in two hours, whereas without the slab it frequently remains incomplete even after eight or ten hours' heating. Tt is not advisable to use a blowpipe, because the chance of mechanical loss is thereby greatly increased. If determinations have to be made frequently, it is preferable to effect the combustion in a muffle furnace, or still more quickly in a platinum boat placed in a heated porcelain tube, through which a current of oxygen is passed. When using the latter, the coal or coke should be broken into small pieces, and not ground fine, or else the oxygen does not come sufficiently into contact with the lower strata. Where frequent tests have to be made, several platinum dishes can be placed in a muffle at the same time. It is best to cover the dishes or boats at first by a mica plate and to remove this only when the gases have been driven off, after which the ignition is continued, until no more black spots are visible and the weight remains constant. 4. Sidphur (Eschka's method). — Mix 0'5 to 1 g. of the finely ground coal with Ij times its weight of an inti- mate mixture of 2 parts of well-burnt magnesia and 1 part of anhydrous sodium carbonate. The mixture is made in a platinum crucible by means of a glass rod, and the crucible, without putting on the cover, is heated in an inclined position, in such manner that only its lower portion attains a red heat. This is most conveniently done by placing it in an asbestos board, provided with a hole, as shown in Fig. 1. The combustion of the sulphides to sulphates should be promoted by frequent stirring with a thick platinum wire ; it will be finished in about an hour, during which time the grey colour of the mixture mostly passes into yellow, red, or brown. The calcined mass is covered with hot water, and bromine water is added until the liquid shows a slight yellow colour. Then heat the whole to boiling, decant the liquid through a filter, and wash the residue with hot water. Add hydrochloric acid to the aqueous solution, boil till all the bromine has been removed and the liquid has been decolorised, and add a solution of barium chloride, drop by drop, always at a boiling heat, until the precipi- tation is complete. If the magnesia or the sodium carbonate employed are not quite free from sulphates, these must be separately estimated and the amount deducted from the total sulphur found. Even if the gas employed for heating the crucible Fig. 1. FUEL AND FURNACES 95 should contain a notable quantity of sulphur, there is no error caused by this, if the products of combustion are kept away from the contents of the crucible by the asbestos shield as shown in the- figure. One part BaS04 indicates 0"1374 part S. 5. The calorific power of fuel can be estimated by ascertaining the percentage of carbon and hydrogen, according to the ordinary methods of elementary analysis, and calculating the results accord- ing to Dulong's formula. In the case of coal it is necessary to take account of the volatile sulphur — that is, that which is determined by heating in a current of oxygen, passing the gases through neutralised hydrogen peroxide, and titrating the sulphuric acid formed. If the percentage of C, H, and (volatile) S, and that of the moisture (W), is known, the percentage of the oxygen is expressed by the equation : — = 100 -(C + H + S + W+ash). The nitrogen contained in the coal may be neglected. The calorific power of the coal, expressed in gram-calories, is then = 81C-F290 ('H--5-^+25S-6■W. A direct estimation of the heating power of fuel can be made by means of the calorimetric bomb, of which a description is given in Tech. Meth., vol. i., p. 254. B. — Furnaces. 1. Chimney Gases. — In these, CO2, O, CO, and N (the latter by diflFerence) are most conveniently estimated by the Orsat apparatus, shown in Fig. 2. This consists of a gas-burette. A, connected with the water-filled level-bottle B by means of a rubber tube. A is filled to the zero point with water, and by lowering B gas is aspirated, either from the supply tube C or from the absorption pipettes, D, E, F. The gas is forced into each of these pipettes by opening its special tap and raising B. For reading the volume of gas in A, the bottle B must be held in such a position that the level of water is the same in A and B. The absorption pipettes are charged as follows ; — Tube D receives 110 c.c. of caustic potash solution of specific gravity 1'20 to 1'28. This absorbs CO2, and can serve for a long time. Tube E serves for absorbing the oxygen by means of very thin sticks of phosphorus, kept under water. This tube, when not in use, should be protected from the light by a covering of black paper. Any tarry matters getting into this tube render the phosphorus inactive, and must therefore be kept out by filtering the gas before entering into C, through asbestos, cotton-wool, or other suitable material. The absorption of the oxygen by the phosphorus only 96 THE TECHNICAL CHEMISTS' HANDBOOK sets in at 16° C, better at 18° C. In case the room is at a lower temperature, the vessel E must be cautiously warmed up by a spirit-lamp. In tube F the carbon monoxide is absorbed. For this purpose a solution is prepared by shaking up in a closed bottle 250 g. cuprous chloride with a solution of 250 g. am- monium chloride in 750 c.c. water. When completed, a spiral of copper wire, reaching from top to bottom, is introduced into the stock bottle. This bottle is always kept well closed when Fig. 2. not in use. Before charging tube F, 3 vols, of the solution from the stock bottle are mixed with 1 vol. liquor ammonise, specific gravity 0*905. One c.c. of this mixture ought to absorb 16 c.cm. CO, but this requires prolonged shaking. The reagent in F must be frequently renewed ; if this is neglected, it may even yield up some CO to gases containing too little of it. The reagent in F also absorbs ethylensj but this gas does not occur in chimney gases. Since the solution in F also absorbs oxygen, the latter must always be removed before employing pipette F. FUEL AND FURNACES 97 For daily use it is mostly sufficient to test merely for CO2, by means of the caustic potash solution in pipette D. Checking the working of Furnaces. — The estimation of CO2 in the chimney gases, if combined with an observation of tempera- ture, admits of checking both the efficiency of a furnace or boiler and the daily work of the firemen, according to a formula worked out by Lunge (Zsch.f. angew. Chem., 1889, p. 240). A consecu- tive number, say from 10 to 15 tests for CfOj, are made by an Orsat apparatus in the flue leading from the furnace to the chimney, and the mean volume percentage of CO2 found is called n. At the same time, a thermometer with very long stem, tightly inserted in the testing hole in such .manner that its bulb is well within the flue, but that the scale can be read ofif outside, is observed at frequent intervals, and the mean temperature of the gases is called t', that of the air outside t. c is the specific heat of a cubic metre of CO2, expressed in gram-calories ; c' that of N or O (see below). The total volume of exit gases produced by the combustion of 1 kg. dF carbon burnt on the grate is = 1"854 -I- 1'854 ( ^ j cubic metres, and the loss of heat in the exit gases, expressed in gram-oalories : — L = 1 -854 ({' - 1!) c + 1 -854 («' - n^^Z±\ c'. The loss, expressed in per cent, of the heat theoretically given out by the carbon, is : — 100 L 8080 The value of c' may be assumed for all temperatures =0"31 ; that of c varies with the temperature, and must be taken as follows : — i' is below 150° C, c=0-41. „ between 150-200° = 0-43. ,» i» 200-250° = 0-44. 250-300° = 0-45. ,, ,, 300-350° = 0-46. Note. — The observations of n and t' must be made several times in succession, and the average value taken as final. For accurate investigations several series of tests must be made at different times of the day. Instruments have been devised for a continuous approximate check of the percentage of CO2 in chimney gases, such as Arndt's CEconometer. 2. Gas from Producers {Generators). — In producer gas usually only CO2 and CO are estimated by means of Orsat's apparatus, as described, p. 95. Any ethylene present in the producer gas would G 98 THE TECHNICAL CHEMISTS' HANDBOOK be absorbed and estimated togetier with the CO. Hydrogen can be estimated in the residue from absorbing COj, CO, C2H4, and O, by mixing it with a measured volume of air, and passing the mixture over gently heated platinum or palladium asbestos.* The estimation is most conveniently done in Lunge's modification of Orsat's apparatus. Fig. 3. The indicating letters correspond to those in Fig. 2, but there is an additional U-tube, G, connected with a capillary, H, of refractory glass. H contains platinum or falladium asbestos and can be heated by the small spirit lamp , turning on a pivot. The U-tube G is filled with water. The gas freed from CO2, CO, C2H4, and O (if this be present) is mixed m the gas-burette A with as much air as the space will allow, and * This can be obtained ready-made or is prepared by soaking a few threads of long soft asbestos in a strong solution of platinum or palladium chloride, mixed with a saturated solution of sodium formate and enough sodium carbonate to produce an alkaliiie reaction. After oneLour's soaking th^ asbestos is dried completely in a water- bath, whereby the metal is precipitated in a very minute state of division. The soluble salts are then washed out by hot water and the asbestos Is again dried. FUEL AND FURNACES 99 a reading is taken. This air will suflSce for a quantity of hydrogen corresponding to ^ of the employed volume of air (i.e. twice the volume of oxygen contained in that air). If more H be present, which will only occur in the case of " water gas," either less than 100 c.c. of gas must be employed at the commencement for the analysis, or the residual gas is mixed with oxygen instead of with air. The capillary tube H is heated very gently by means of the lamp I, and the gaseous mixture is quickly passed once through it into G and back again, when one end of the platinum asbestos should become red hot. The residual gas is again measured and f of the diminution in volume .calculated as hydrogen. If methane (marsh gas, CHj) is to be estimated, the residue from the last operation is mixed with more air and burnt by means of an electrically heated palladium or platinum wire, enclosed in a capillary tube. If a capillary platinum tube is employed, filled with a few platinum wires, so as to leave a very small space for the gases to pass through, the electric heating may be replaced by that of a broad gas flame, producing a strong red heat. 3. Speed of Draught. — A convenient apparatus for measuring this in chemical works, where any fine mechanism would soon be ruined, is Fletcher's anemometer, based upon the movement of a column of ether in a U-tube (described in Lunge's Sulphuric Add amd Alkali, 4th edition, vol. i., p. 768). Fig. 4 shows this in the simpler form, leaving out the microscopes, which are quite unnecessary for reading the divisions of the scale or the vernier. The ends of the glass tubes a b should be placed rather less than one-sixth of the diameter of the flue from its inner wall. The straight end of a ought to be as exactly parallel as possible to the 100 THE TECHNICAL CHEMISTS' HANDBOOK direction of the draughts ; the end of 6 ought to be exactly at a . right angle to this, and so that the current blows straight into it. Without this precaution a mistake is made, which is avoided by the arrangement shown in Fig. 5, and proposed by Hurter, viz., employing tubes with ends bent in opposite directions. The tubes a h communicate with the ether tube c d ; the draught causes the ether to rise in a by aspiration and to fall in 6 by the pressure of the air blowing into the tube. The difference of level between c and d is read off by means of the scale and vernier. The sliding disc e is then turned through 180°, whereby the currents are reversed. There will now be a difference of levels in the opposite direction, but equal in amount to the first, if the observation is correct. The sum of these two differences is the " anemometer reading " given in the tables. The following tables show the application of the readings of the Anemometer for calculating the speed of draughts, both for instru- ments graduated on the inch scale and for those on the metrical scale. o.— TABLE TO SHOW THE SPEED OP CnRRBNTS OF AIR. At a temperature of 15' C.=60° F. ; Barometer, 760 mm. = 29-92 inches. A. — Readings in Inches. Anemom- Speed. Anemom- Speed. Anemom- Speed. Anemom- Speed. eter Feet eter Feet eter Feet eter Feet Beading. per Beading. per Beading. per B«ading. per Inches. Second. Inches. Second. Inches. Second. Inches. Second. •01 2'855 ■16- 11^42 •32 16^15 •95 27-83 •02 4 •038 •17 11^77 •34 16^65 1-00 28-55 •03 4^945 -18 12^11 •36 17^13 ^25 31-93 ■04 o^7lO -19 12^45 •38 17^60 1^50 34^97 •05 6 ■384 •20 12^77 •40 18-06 1^75 37^77 •06 6^993 •21 13^08 •45 19^15 2^00 40 •S? •07 7^554 •22 13^39 •50 20-18 • •• •08 8-075 •23 13^70 •55 21-17 •09 8-666 •24 13^99 •60 22^12 .•. •10 9-028 •26 14^28 •65 23-02 •11 0-469 •26 14 •se •70 23-89 •12 9-891 •27 14^84 •75 24-73 • <• •13 10-29 •28 15^11 •80 25-54 • *• •14 10 •es •29 15 •as •85 26^32 ... ■15 11 •oe •30 15^64 •90 27 •OS ... "' , FUEL AND FURNACES B. — Readings in Millimetres. 101 Bead- ing. Speed. Bead- ing. Speed. Bead- ing. Speed. Bead- ing. Speed. Bead- ing. Speed. Bead- ing. Speed. mm. m- mm. m. mm. m. mm. m. mm. m. mm. m. 0-1 0-676 1-4 2-040 2-7 2-833 6-0 3-866 10-0 6-462 19-0 7-515 0-2 0-771 1-6 2-111 2-8 2-886 6-2 3-931 10-6 6-586 20-0 7-710 0-S 0-944 1-6 2-181 2-9 2-936 6-4 4-006 11-0 6-718 21 7-900 0-4 1-090 1-7 2-248 3-0 2-986 5-6 4-080 11-6 6-846 22 8-086 0-5 1-205 1-8 2-313 3-2 8-077 6-8 4-162 12-0 6-972 23 8-268 0-6 1-341 1-9 2-376 8-4 3-179 ■ 6-0 4-223 12-5 6-096 24 8-446 0-V 1-442 2-0 2-43S 3-6 3-271 6-6 4-896 13-0 6-216 25 8-620 0-8 1-560 2-1 2-498 3-8 8-361 7-0 4-661 13-6 6-834 80 9-443 0-9 1-636 2-2 2-667 4-0 3-448 7-5 4-721 14-0 6-460 36 10-199 1-0 1-724 2-3 2-615 4-2 3-469 8-0 4-876 16-0 6-667 40 10-903 1-1 1-808 2-4 2-671 4-4 3-616 8-6 6-026 16-0 6-896 45 11-566 1-2 1-889 2-6 2-726 4-6 3-69S 9-0 6-172 17-0 7-108 50 12-190 1-S 1-966 2-6 2-779 4-8 8-777 9-5 6-314 18-0 7-314 /3.— CORRECTIONS FOR TSMPEiRATOREi. Column a shows the temperature of the chimney or flue, column h the factor for multiplying the figure found in Table a in order to arrive at the real speed of the current of gas. A. — Readings In Degrees Fahrenheit. Fahr. ' a. l>. „. ft. * h. u- 6. 1-0634 90 0-9723 180 . 0-9012 380 0-7865 5 1-0577 95 0-9679 185 0-8977 400 0-7763 10 1-0520 100 0-9636 190 0-8943 425 0-7663 15 1-0464 105 0-9593 195 0-8909 450 0-7556 20 1-0409 110 0-9661 200 0-8875 476 0-7454 26 1-0355 115 0-9509 210 0-8808 500 0-7366 30 1 -0302 120 0-9468 220 0-8743 625 0-7261 35 1-0250 125 0-9428 230 0-8680 560 0-7171 40 1-0198 130 0-9388 240 0-8614 575 0-7085 45 1-0148 135 0-9348 250 0-8567 600 0-7000 50 1-0098 140 0-9309 260 0-8497 650 0-6841 55 1-0049 145 0-9270 270 0-8438 700 0-6691 60 1-0000 160 0-9232 280 0-8380 750 0-6552 65 0-9952 165 0-9194 290 0-8324 800 0-6420 70 0-9905 160 0-9166 300 0-8269 860 0-6297 75 0-9858 165 0-9119 320 0-8163 900 0-6181 80 0-9812 170 0-9083 340 0-8060 960 0-6070 85 0-9767 175 0-9047 360 0-7960 1000 0-5964 102 THE TECHNICAL CHEMISTS' HANDBOOK B.- —Readings In Decrees Centigrade. a. ro. t. a. t°C. b. a. f C. b. a. rc. t. a. fC. t. a. r.'C. 6. -10 1-046 IS 0-996 42 0-956 66 0-922 140 0-835 260 0-735 5 1036 20 0-991 44 0-953 68 0-919 160 0-825 270 0-728 1-027 22 0-988 46 0-950 70 0-916 160 0-815 280 0-721 2 1-023 24 0-985 48 0-947 76 0-909 170 0-S06 290 0-715 4 1-020 26 0-981 50 0-944 80 0-903 180 0-797 300 0-709 6 1-016 28 0-978 52 0-941 85 0-897 190 0-788 320 0-697 8 1-012 30 0-975 54 0-938 90 0-890 200 0-780 340 0-686 10 1-009 32 0-972 66 0-935 95 0-884 210 0-772 360 0-676 12 1-005 34 0-968 58 0-933 100 0-878 220 0-764 400 0-654 14 1-003 86 0-965 60 0-930 110 0-867 230 0-766 450 0-631 IB 1-000 38 0-962 62 0-927 120 0-856 240 0-749 500 0-603 16 0-998 40 0-959 64 0-924 130 0-845 260 i 0-742 . A very simple and cheaper instrument is Seger's Differential Anemometer, Fig. 6. Tte U-tube A is surmounted by two enlargements, B and C. D is a sliding scale, adjustable by slits a a and screw- ji-Maaii -B, pins 6 6. The tube is filled with two non- % \ riMT 1 miscible liquids of nearly equal specific ! i! '1 m t B gravity ; for instance, paraffin oil and dilute spirits of wine (coloured). The line of con- tact, at X, is the zero point of the scale D. If an aspirating force is acting on the sur- face of the liquid in C, the level of the liquid will be raised in C, and the point X will be lowered in a multiplied ratio, corre- sponding to the difference in the sectional areas of the narrow part of A and the enlargements in C, say 1 :^0. C. — Temperature. The measurement of temperatures up to about 300° calls for no special remark, as the ordinary mercurial thermometers are always used. For higher temperatures a large number oi pyrometers have been con- structed. All of these are unreliable after prolonged use, many of them even from the very beginning, and they require a frequent control of their indications by calorimetric methods. Among these "empirical" pyrometers those mostly used are : Gauntlett's (up to 900° C. or 1600° F.), Steinle and FUEL AND FURNACES 103 Hartung's graphite pyrometer (up to 1200° C), and Klinghammer's Thalpotasimeter. In many cases Prinsep's metallic alloys, of definite fusing points, and Seger's cones, do good service ; the fusing points corresponding to the commercial forms of these have been given on p. 35. The calorimetric control can be effected by any of the well- known calorimeters, such as Mahler's or Fischer's, but is a some- what difficult and complicated operation, and the working of the air pyrometer is even more so. Most of the drawbacks formerly connected with pyrometry have been removed by the construction of Le Chatelier s Thermo- dectric Pyrometer. Its working part is shown in Fig. T. It con- sists of a thermocouple, composed of a wire a of pure platinum, and a wire b of an alloy of 90 parts of platinum +10 parts of rhodium, soldered to the former. These wires are insulated by porcelain tubes c, d, about 3 feet long, and protected on the out- side, against heating gases, by the iron pipe e e. The wiresjare •^ 1000 mm PiQ. 7. connected vrith platinum or copper wires, leading to a galvan- ometer, and the indications of the needle of the latter show the temperature at the point where a and b are soldered together. The temperature scale marked on the galvanometer is fixed by comparing it with an air pyrometer at the works where the instruments are made. The following rules must be observed for the use of this pyrometer. The galvanometer should be placed in a horizontal position and so as to be protected against mechanical oscillations, preferably on a wall-bracket, and this may be at some distance from the pyrometer itself — e.g. in the manager's office. Before moving the galvanometer from its place, the needle should be always arrested. After fixing it on its bracket, the arresting- screw is cautiously loosened, until the needle begins to move. If it does not point to zero after being placed in a horizontal position, this must be effected by moving the adjusting screws. 104 THE TECHNICAL CHEMISTS' HANDBOOK The electric resistance of the conducting wire should not appreci- ably exceed- 1 ohm ; up to distances of about 300 feet this will be attained by employing insulated copper wire of ^-inch thickness. The junction of the couple with the conducting wires ought not to be much above the ordinary temperature. If one of the wires should break, the contact can be re-established by twisting the ends tightly together for a length of about ^ inch ; it is preferable to fuse them together in an oxyhydrogen flame. If the tempera- ture within the furnace does not exceed 1000°, the pyrometer may be left permanently inside ; for higher temperatures, which would cause the iron pipe to soften and to burn away too rapidly, the pyrometer should be taken out and introduced merely for taking an observation, which may be done ten minutes afterwards. Even then it is best to provide a fireclay slab on which the instrument can rest. Le Chatelier's pyrometer may be employed for temperatures up to 1500° C. For higher temperatures, up to 2100°, W. C. HeriBus (Hanau, Germany) has constructed a thermo- couple, consisting of a wire of piire iridium, fused to another wire of an alloy of 90 parts iridium -I- 10 ruthenium. For such high temperatures Wanner's pyrometer is now fre- quently used. It allows a photometric comparison of the polarised light from a small electric lamp with that of "the furnace, etc., to be tested, by means of an instrument like a telescope ; it is easy to handle, and is serviceable for approximately measuring tempera- tures above 1500°, where Le Chatelier's pyrometer cannot be employed. It is also more convenient than the latter for estimat- ing temperatures inside the furnace at some distance from the front of the furnaces. (Supplied by Townson & Mercer, London.) D. — Peed-Water for Steam-Boilers, etc. 1. Hardmess. — The English degrees of hardness are based on the unit of 1 part CaCOa, or its equivalent of MgCOs, in 70,000 parts of water (grains to the gallon). The French degrees signify each 1 part CaCOs (or MgCOa) in 100,000 water, the German degrees that of 1 part CaO (or MgO) in 100,000 water. The testing for hardness was formerly mostly effected by Clark's soap test. The methods to be described here are both simpler and more accurate than the soap test. (a) Temporary Hardness (alkalinity) is that which is removed by prolonged boiling, by which operation nearly all the GaCOa and some of the MgCOs is precipitated. This can be estimated with sufficient approximation by testing the water alkalimetrically, employing \ normal hydrochloric acid and methyl orange as indi- cator, at the ordinary temperature, until the first reddish tint appears. "When employing 200 c.c. of the water for this test, the number of c.c. of ^ normal acid used, multiplied by 3'5, indicates FUEL AND FURNACES 105 the English degrees of temporary hardness (for French degrees multiply by 5, for German degrees by 2 '8). Where feed-water, purified by means of sodium carbonate, is tested in this way, an error may be caused by the presence of an excess of Na2C03, which makes the hardness appear too high. In such cases the 200 c.c. of water employed should be boiled in a porcelain dish for some time, the precipitated carbonates removed by filtration, and the filtrate titrated as above. The acid then used corresponds to the Na^COa and a little unpre- cipitated MgCOs- (b) Total Hardness. — Add to 200 c.c. of the feed-water hydro- chloric acid in slight excess, boil down to about 50 c.c. ■ wash this into a 100 c.c. flask, neutralise exactly with caustic soda solution, employing methyl orange as indicator ; add 20 c.c. of a mixture of equal volumes of J normal caustic soda solution and \ normal sodium carbonate solution, boil, allow to cool, fill up the flask to the 100 c.c. mark with distilled water, pour through a dry filter, and estimate the unsaturated alkali in 50 c.c. of the filtrate by ^ normal hydrochloric acid and methyl orange. Multiply the c.c. of acid used by 2, and deduct this from 20; the remainder = a shows the alkali consumed for precipitating the alkaline earths contained in 200 c.c. of water. The total hardness is hence, = 3"5(x in English degrees, 5a in French, 2"8a in German degrees. This process is accurate also in presence of magnesia. By deducting the degrees of alkalinity found in a from the total hardness found in 6, the permanent hardness is obtained — i.e. that which is caused by calcium sulphate. Water having- a total hardness of less than 8° (English) is considered as soft, from 8° to 15° as moderately hard, above 15° as hard. (c) Residue on Evaporation. — In the case of water containing but little MgO, a convenient check for the total hardness — i.e. the sum of alkalinity a and permanent hardness 6 — is afforded by evaporating 500 c.c. down to dryness, heating to decompose the organic matter, moistening with a solution of CO2 in distilled water, and drying at 110°. Since the degrees of hardness are all calculated for CaO, the value of c will not be quite equal to a+h, if any considerable quantity of magnesia is present, and this indirectly proves the presence of more magnesia than usual. 2. Estimation of the Reagents (lime water and sodium, carbonate) required for Purifying Water. — Add to 500 c.c. of the water 10 c.c. of a ^ normal sodium carbonate solution, evaporate to dry- ness, take up the residue with a small quantity of water, filter through a small filter, wash till there is no further alkaline reaction, and estimate the unconsumed sodium carbonate in the 106 THE TECHNICAL CHEMISTS' HANDBOOK filtrate plus washings by titrating with methyl orange and ^ normal hydrochloric acid. If a c.o. of \ normal sodium carbonate are used in the titration, then 2ax0'0106 shows the grams of pure sodium carbonate required per litre of the water for removing the calcium sulphate — i.e. the permanent hardness. _ The amount of lime water required for removing the temporary hardness is estimated as follows : — To 500 c.c. of water add 100 c.c. of clear lime water, after having previously determined its percentage of CaO by titrating with ^ normal hydrochloric acid and phenolphthalein (methyl orange is not applicable in this case, because this would indicate also the CaCOs present in small quantities along vdth Ca(0H)2, which would be wrong). Heat the mixture during half an hour in a covered flask (to keep out CO2), allow to cool, pour through a dry filter, and titrate, without delay, 500 c.c. of the filtrate. The HCl now used, increased by one-fifth (since the original 500 c.c. of water had been brought to 600 c.c), shows the quantity of lime not used up. By deducting this from the CaO originally contained in 100 c.c. of the lime water, the quantity of CaO required for destroying the temporary hardness of § litre of the water to be tested is ascertained. II. SULPHURIC ACID MANUFACTURE. A. — Brimstone. 1. Moislmre.^-Hhis, should be estimated by drying an average sample of 100 g. at 70° for a few hours, in an oven or water-bath. The sample must be prepared without losing any moisture during the operation ; the brimstone for this purpose must, therefore, not be ground, but only coarsely crushed, as quickly as possible. 2. Bituminous Substances (Fresenius). — Eemove the sulphur by heating the sample for some time a little over 200°, taking care that it does not take fire, weigh the residue, and deduct the ash found in No. 3. 3. Ash. — Bum 10 g. in a porcelain dish and weigh the residue. Some samples of brimstone contain carbonaceous matter. In this case (which is easily recognised by the appearance of the sample) the flame must be removed immediately after the sulphur has been burned, and before the carbon has taken fire, so that the latter is not calculated as sulphur. 4. Arsenic. — Treat 10 g. brimstone with dilute liquor ammonise at 70° to 80°, in order to dissolve the AS2S3, filter, neutralise the filtrate exactly with dilute nitric acid, and titrate with dcci- SULPHURIC ACID MANUFACTURE 107 normal silver nitrate solution, until a drop gives a brown colour with a solution of neutral potassium chromate. Each c.c. of the silver nitrate solution indicates 0'041 per cent. AS2S3. If the arsenic should be present as ferric or calcium arsenate (this never occurs in the case of native brimstone, but it may do so in the case of sulphur recovered from Leblanc soda residue), the sample must be extracted with' carbon disulphide, the residue oxidised by aqua regia, and the sulphur estimated as in pyrites (see below). 5. Direct Estimation of Svlphur (Macagno, Ghem. News, v., 43, p. 192). — Fifty g. of the finely ground brimstone are dis- solved in 200 c.c. carbon disulphide by digesting in a stoppered bottle at the ordinary temperature, and the specific gravity of the liquid =s is estimated. This must be reduced to the specific gravity at 15°=S, by means of the formula (valid up to 25° C.) S,=s-I-0'0014(<-15°). The following table gives, for each valueof S, the percentage in this solution, which number must be multi- plied by 4 to indicate the percentage of sulphur in the sample of brimstone : — Specific G-ravities of Solutions of Sulphur in Carbon Disulphide at 15° (referred to Water of 4°). Spec. y Spec. X Spec. % Spec. / Spec. % Grav. ^ Grav. S Grav. ^ Giav. •3 Grav. 8 1-271 1-296 6-0 1-321 12-1 1-846 18-1 1-371 25-6 1-272 0-2 1-297 6-3 1-322 12-3 347 lS-4 1-372 26-0 1-273 0-4 1-298 6-5 1-323 12-6 348 18-6 1-373 26-5 1-274 0-6 1-299 6-7 1-324 12-8 349 18-9 1-374 26-9 1-275 0-9 1-SOO 7-0 1-325 13-1 350 19-0 1-375 27-4 1-276 1-2 1-801 7-2 1-826 13-3 351 19-3 1-376 28-1 1-277 1-4 1-302 7-6 1-327 13-5 352 19-6 1-377 28-6 1-278 1-6 1-30S r-8 1-328 13-8 363 19-9 1-378 29-0 1-279 1-9 1-304 8-0 1-329 140 354 20-1 1-379 29-7 1-280 2-1 1-306 8-2 1-330 14-2 355 20-4 1-380 30-2 1-281 2-4 1-306 8-6 1-331 14-5 356 20-6 1-381 80-8 1-282 2-6 1-307 8-7 1-332 14-7 367 21-0 1-382 31-4 1-283 2-9 1-308 8-9 1-333 15-0 358 21-2 1-383 31-9 1-284 8-1 1-309 9-2 1-334 15-2 359 21-6 1-384 32'6 1-285 3-4 1-310 9-4 1-3S5 15-4 360 21-8 1-385 33-2 1-286 3-6 1-311 9-7 1-336 15-6 861 22-1 1-386 33-8 1-287 3-B 1-312 9-9 1-837 15-9 362 22-3 1-387 34-6 1-288 4-1 1-313 10-2 1-338 16-1 363 22-7 1-388 85-2 1-289 4-4 1-B14 10-4 1-339 16-4 364 23-0 1-389 36-1 1-290 4-6 1-316 10-6 1-340 16-6 365 23-2 1-890 86-7 1-291 4-8 1-316 10-9 1-341 16-9 386 23-6 1-391 37-2 1-292 6-0 1-317 11-1 1-342 17-1 367 24-0 (satui !ihaf1\ 1-293 5-3 1-318 11-3 1-343 17-4 368 24-3 aoea; 1-294 6-6 1-319 11-6 1-344 17-6 369 24-8 1-295 6-8 1-320 11-8 1-345 17-9 1-370 25-1 108 THE TECHNICAL CHEMISTS' HANDBOOK 6. Selenium, is found by fusing a sample with potassium nitrate, dissolving the mass in hydrochloric acid, and treating with sulphur dioxide, which precipitates the selenium. 7. The degree of fineness of ground brimstone is estimated in France by means of Chancel's sulphurimeter, i.e. a glass tube, closed at one end, provided with a glass stopper at the other, and graduated in 100 parts. In this, the ground brimstone is shaken up for some time with pure, anhydrous ether, and after allowing the tube to rest in a vertical position, the number of divisions occupied by the brimstone is read oflf (degrees Chancel). B. — Spent Oxide of Gas-works. See "Ooal-Gas.' C. — Pyrites. 1. Moisture. — The ground pyrites is dried at 105° C. tiU the weight remains constant. For the following tests the pyrites is not employed in the dried state, but the finely ground average sample, kept in a well-sealed bottle. Compare the Appendix as to taking and reducing an average sample. The analytical results are calculated for dry pyrites, for which purpose a special estimation of moisture is made with the average sample. 2. Sidphur (Lunge's method). — About 0"5 g. of pyrites is treated with abOut 10 c.c. of a mixture of 3 vols, nitric acid (specific gravity 1'4) and 1 vol. strong hydrochloric acid, both ascertained to be absolutely free from sulphuric acid, due care being taken to avoid all spurting. Quite exceptionally, the separation of a little free sulphur will be observed ; if this takes place, the sulphur must be oxidised by adding a little potassium chlorate. Evaporate to dryness on a water-bath, add 5 c.c. hydrochloric acid, evaporate once more (no nitrous fumes ought to escape now), add 1 c.c. concentrated hydrochloric acid and 100 c.c. hot water, filter through a small filter, and wash with hot water. The insoluble residue may be dried, ignited, and weighed. It may contain, besides silicic acid and silicates, the sulphates of barium, lead, and even calcium, the sulphur of which, as being useless, is purposely neglected. The filtrate and washings are saturated with ammonia, avoiding much excess and keeping the liquid at 60°-70° for about ten or fifteen minutes before filtration, but Twt boiling, till all the ammonia is expelled (in which case the precipitate contains some basic sulphate). The precipitated ferric hydroxide is filtered and washed. This can be done in from half to one hour, by employing the following pre- SULPHURIC ACID MANUFACTURE 109 cautions : (1) Filter hot, and wasli on the filter with hot water, avoiding channels in the mass, but so that the whole precipitate is thoroughly churned up with the water each time (washing by decantation would produce too great a bulk of liquid) ; (2) employ sufficiently dense, but rapidly filtering paper; (3) use funnels, made at an angle of exactly 60°, whose tube is not too wide, and is completely filled by the liquid running through. A filter pump may also be employed, with the usual precautions. Wash till about 1 c.c. of the washings, on adding BaCl2, shows no opalescence, even after a few minutes. (If there is any doubt on this point, the complete absence of basic sulphates should be investigated by drying the precipitated ferric hydroxide, fusing it with pure sodium carbonate, and testing the aqueous solution of the melt for sulphates.) The filtrate and washings should not appreciably exceed 300 c.c, or else should be concentrated by evaporation. Acidulate with pure hydrochloric acid in very slight excess, preferably by adding acid till methyl orange is just reddened, and then adding just 1 c.c. of strong HCl. Then heat to boiling, remove the burner, and add a solution of BaClj, previously heated to boiling. A large excess of BaClj must be decidedly avoided. For 0'5 g. pyrites, 20 c.c. of a 10 per cent, solution of BaCl2 is always more than sufficient. This is roughly measured off in a test-tube, pro- vided with a mark, and heated in the same tube ; it is then poured into the hot liquid all at once, not drop by drop. It is true that this procedure will cause a little barium chloride to be carried down along with the sulphate, but the error caused by this just compensates the opposite error, caused by the slight solubility of barium sulphate in the hot solution, containing free HCl and ammonium chloride. After precipitation the liquid is left to stand for half an hour, when the precipitate should be completely settled. It is quite unnecessary to wait for a longer time, as is sometimes prescribed ; this is not merely a waste of time, but it unnecessarily retards the work by the cooling of the liquid. Decant the clear portion as carefully as possible through a filter, pour 100 c.c. boiling water on the precipitate, and stir up. Wait two or three minutes, when the liquid ought to have settled completely, and decant again. Repeat the treatment with boiling water, and the decantation, three or four times, till tha liquid ceases to give an acid reaction. Wash the precipitate on to the filter, dry, and ignite. It should be a perfectly white and loose powder. One part of it is equal to 0'13743 sulphur. 3. Copper. — The method employed at the Duisburg Copper Works, in its most recent form, is as follows : — Of the powdered pyrites, dried at 100° C, 5 g. is gradually dissolved in 60 c.c. of nitric acid, spec. grav. 1'2, in a flask placed in a slanting position. no THE TECHNICAL CHEMISTS' HANDBOOK When the first violent reaction is over, the flask is heated and the evaporation continued until thick, white fames of sulphuric acid escape. Dissolve the dry residue in 50 c.c. hydrochloric acid, spec, grav. 1'19, add 2 g. sodium hypophosphite, dissolved in 5 c.c. water, for the purpose of removing the arsenic and reducing the ferric chloride, boil for some time, then add an excess of concen- trated hydrochloric acid, diluted with about 300 c.c. hot water, pass hydrogen sulphide into the liquid, separate the precipitate from the liquid by filtration, and wash it well. Pierce the filter paper with a glass rod, wash the precipitate back into th6 precipi- tating flask, dissolve the sulphides adhering to the filter and the principal portion of the precipitate by means of nitric acid, and evaporate the contents of the flask to dryness on the water-bath. Treat the residue with nitric acid and water, neutralise with ammonia, and add sulphuric acid in slight excess. After the liquid has cooled down, separate the clear liquid from the insoluble lead sulphate, etc., wash out the flask and filter with water con- taining a little sulphuric acid, add to the filtrate 3 to 8 c.c. nitric acid, spec. grav. Vi, and precipitate the copper electrolytically. From the ascertained percentage of copper deduct O'Ol per cent, for bismuth and antimony. 4. Lead remains in the residue from the treatment with aqua regia (No. 2) or nitric acid (No. 3), as lead sulphate. This is extracted from the residue (preferably that from the nitric acid treatment) by heating with a concentrated solution of ammonium acetate. The solution is evaporated, with addition of a little pure sulphuric acid, the evaporation completed in a porcelain crucible, and the residue dried and ignited. One part PbS04 =0-6831 Pb. 5. Zinc is sometimes estimated in pyrites, because the sulphur combined with it is hardly recoverable in the pyrites burners. The following method (communicated to the author by Messrs Hassreidter and Prost) should be employed in this case, in lieu of Schaflher's method described subsequently for zinc blende, because in the case of pyrites the presence of iron renders gravimetric preferable to volumetric analysis : — Dissolve 1 g. pyrites in aqua regia, as described on p. 108, expel the nitric acid, take up the residue with about 20 c.c. concentrated hydrochloric acid, dilute with water, treat the acid solution with HjS in order to precipi- tate lead, etc., filter, expel the H2S from the filtrate by boiling, and oxidise the liquid with aqua regia. When cooled down, add ammonium carbonate until the precipitate formed redissolves but slowly, then add ammonium acetate, boil for a short time, and filter the liquid from the precipitated basic ferric sulphate. As this contains a little zinc, dissolve it in hydrochloric acid, precipitate it again as above, and repeat this treatment until no SULPHURIC ACID MANUFACTURE 111 more zinc is found in the filtrate. Hie united filtrates are concentrated by evaporation. Then precipitate the zinc in the hot solution by HaS, allow to stand for twenty-four hours, pour off the clear liquid, filter, wash the ZnS, dissolve it (without removing the filter) in dilute HCl, boil off the HjS, precipitate with sodium carbonate, wash the ZnCOs, dry and ignite it. One part ZnO=0'8034 Zn. For very accurate work the SiOa, FeaOs, and AI2O3 retained in the ZnO should be estimated and deducted, but this is very rarely necessary. 6. The Carbonates (of Ca, etc.) are sometimes estimated in pyrites, because they convert a certain quantity of sulphur into sulphate. Since their quantity is always small, the CO2 is estimated directly by expelling with strong acids, and is easily estimated gravimetrically by absorbing it in soda-lime, etc., or, more accurately and quickly, by the volumetrical process of Lunge and Rittener, which will be described later on in connection with the analysis of carbonated spda liquors. v. Arsenic. — Eeich's method, modified by M'Cay : — Decompose 0"5 g. pyrites by concentrated nitric acid in a porcelain crucible, remove the free acid by evaporation, but not to complete dryness, add 4 g. sodium carbonate, heat on the sand-bath untU the mass is quite dry, add 4 g. potassium nitrate, and heat until the mass has fused quietly for ten minutes. After cooling, wash it with hot water, acidulate the filtered solution with a little nitric acid, heat for some time till all CO2 is expelled, add silver nitrate, and neutralise carefully with dilute ammonia. The precipitate fornied contains all the arsenic as AggAsO^. Dissolve it in dilute nitric acid, and either estimate the silver volumetricaUy by ammonium thiocyanate (Volhard's method), or evaporate the solution in a porcelain dish, dry, and weigh the residue. One part Ag3As04= 0-1620 As, or 1 part Ag=0-2316 As. D. — -Burnt Pyrites (Cinders). 1. Sulphur. — Mix exactly 2 g. sodium bicarbonate of known alkalimetric value, in a nickel crucible of 20 or 30 c.c. capacity, intimately with 3'207 g. of ground cinders, by means of a glass rod flattened at the end. Heat the crucible by a small gas-flame, the point of which reaches just to the bottom of the crucible for ten minutes. Stir the mass up again, heat it again for fifteen minutes by a stronger flame, but not to the fusing point. During the heating the crucible should be covered, and no stirring should take place during this time, to prevent the escaping CO2 from carrying away any dust. Empty the contents of the crucible into a porcelain dish, wash it out with water, add a concentrated 112 THE TECHNICAL CHEMISTS' HANDBOOK solution of sodium chloride, free from magnesium chloride and perfectly neutral (without this addition it is difficult to avoid some ferric oxide passing through the filter later on), boil for ten minutes, filter, wash the insoluble residue till there is no alkaline reaction, allow the filtrate, etc., to cool down, and titrate it with methyl orange and normal hydrochloric acid (1 c.c.=0'05300 NaaCOa, indicating 0'01604 S). If we call the number of c.c. of the acid required by 2 g. bicarbonate = a, and the c.c. of acid used for titrating =6, the percentage of sulphur in the cinders corresponds to ^^— . 2. Copper is estimated as in fresh pyrites (p. 109), but the solution of 1 g. of the sample is effected by hydrochloric acid with only a few drops of nitric acid, and no deduction for Bi and Sb is made from the electrolytically estimated Cu. 3. Iron. — Dissolve 0"5 cinders in concentrated hydrochloric acid by prolonged heating ; reduce the boiling solution by zinc, free from iron, or more conveniently by stannous chloride, the excess of the latter being removed by a little mercuric chloride solution ; pour the solution thus obtained into a half-litre of water, to which about 2 g. manganous sulphate has been added, and which has been just reddened by one or two drops of potas- sium permanganate. Determine the iron by titrating with deci- normal potassium permanganate, each c.c. of which indicates 0'005584 g., or in 0"5 g. cinders 1'117 per cent. Fe. E. — Zinc Blende. 1. Total Sidphur. — Decompose 0"5 of the finely ground sample by pure fuming nitric acid, cooling the beaker until the first violent reaction is over, and add hydrochloric acid, drop by drop, gently heating, until the decomposition is finished. Eemove the iron by precipitation with ammonia, as in the case of pyrites (p. 108), and precipitate the sulphate by adding the requisite quantity of the dilute hot solution of barium chloride, all at once, in which case the BaS04 remaining in solution is just compensated by the BaCl2 carried down with the precipitate (compare p. 109). 2. Zinc. — The following modification of Schaffner's method is employed at the Rhenish and Belgian zinc works, as com- municated to the author by Messrs Hassreidter and Frost : — Treat 2'5 g. of the finely ground blende (dried at 100° C.) in a 250 c.c. Erlenmeyer flask with 12 c.c. fuming nitric acid, first without heating, then heating gently until no more red vapours come off. Add 20 to 25 c.c. concentrated hydrochloric acid, evaporate to dryness on a sand-bath, dissolve in 5 c.c. hydrochloric acid and a SULPHURIC ACID MANUFACTURE 113 little water, heat for some time, add 50 or 60 c.c. water, and heat to 60 or 70° C. until everything except gangue and sulphur has passed into solution. Pass a moderate current of HjS into the solution, and gradually add, with continuous stirring, 50 to 100 c.c. water, until all Pb and Cd have been precipitated. This will be recognised by the fact that the bubbles of gas evolved are transparent. _ Any excessive dilution or too much prolonged treatment with HjS must be avoided. Filter and wash with 100 c.c. sulphuretted hydrogen water, to which 5 c.c. hydrochloric acid has been added, until a drop of the filtrate gives no reaction for zinc with ammonium sulphide. Boil the filtrate and washings (together about 300 c.c.) in order to expel the HjS (test by lead paper), and oxidise the ferrous salt by adding 5 c.c. concen- trated nitric acid and 10 c.c. hydrochloric acid. When partially cooled down, put the solution into a half -litre flask, add 100 c.c. liquor ammonise (specific gravity 0*9 to 0'91) and 10 c.c. of a cold saturated solution of ammonium carbonate, shake well and allow to cool. This solution we call A. In the meantime an ammoniacal zinc solution of known strength, the "titre," is prepared by dissolving a quantity of chemically pure zinc, approximately equal to that contained in the ore, in another half -litre flask, in 5 c.c. nitric acid +20 c.c. hydrochloric acid, adding 250 c.c. water, 100 c.c. liquor ammonise, and 10 c.c. of ammonium carbonate solution, shaking up and allowing to stand till cool. (If manganese be present, add 10 c.c. hydrogen peroxide before adding the liquor ammonise.) This solu- tion we call B. When all is cool, fill both flasks up to the mark, and filter the solution A (made from the ore) through a dry pleated filter. For the titration itself take from each of the solutions A and B 100 c.c, run this into stout glass cylinders ("battery glasses ") and dilute each with 200 c.c. water. The titration is effected by a concentrated solution of commercial crystallised sodium sulphide, diluted with ten or twenty times its volume of water and indicating per c.c. 0*005 to O'OIO g. Zn. This solution is placed in two 50 c.c. burettes, standing side by side, and is run by turns into the zinc solutions A and B. At first 2 or 3 c.c. less than is ultimately required is run in. Agitate the solutions and place at the same time a drop of each, by means of a thin glass rod, on to a strip of sensitive lead paper. After the action has lasted fifteen or twenty seconds, blow away the drops by means of a small wash-bottle and continue the addition of NajS, until both drops, after acting for the same time, produce a slight but distinct brownish colour of the same intensity. If too much liquid has been used in these drop tests, the titration must be repeated once or twice ; at all events, the final reaction must take place equally in both glasses, and the readings must be accurate to 0-05 C.C. ' If we call the quantity of pure zinc weighed out as ".titre " H 114 THE TECHNICAL CHEMISTS' HANDBOOK a, that of the c.c. sodium sulphide solution used for the " titre " b, and the c.c. used for 100 c.c. of the ore solution (=0'5 g. ore) c, the expression — ; — gives the percentage of zinc in the ore. 6 For exact estimations, a quantity of ferric chloride, equal to the content of iron in the ore, is added to the " titre," in order to meet the objection that the ferric hydroxide may carry down a little zinc. Some blendes, containing a large proportion of silicates, obstin- ately resist the ordinary meuiods of testing (Jensch, Zsch.f. angew. Chem., 1894, p. 155). 3. Lead. — The sulphides precipitated in No. 2 are, if necessary, digested with a concentrated solution of sodium sulphide ; then dilute, filter, wash the residue, dissolve it (together with the filter) in nitric acid (sp. gr. 1"20), filter, add an excess of sulphuric acid, evaporate to dryness, and weigh the lead as sulphate. One part PbSO4=0-6831 Pb. 4. Lime and Magnesia are estimated, because they form sulphates in the roasting process. Digest 2"5 g. blende with 50 c.c. dilute sulphuric acid (1 : 10), with application of heat, decant the clear portion ; repeat this treatment once or twice, wash the residue, expel the HgS from the filtrates by boiling, oxidise with bromine water, precipitate with ammonium carbonate, and in the filtrate precipitate first the calcium by ammonium oxalate (weigh this as CaO after strongly igniting), and in the filtrate from this the magnesium by ammonium phosphate (com- pare p. 148). 5. Arsenic is estimated as described on p. 111. 6. Car6(»i.2)ioa;idemaybeestimatedasinpyrites,p. 111. This is useful, even when CaO and MgO are estimated, since blende contains sometimes ferrous and zinc carbonate. 7. Available Svlphur. — From the total sulphur found in No. 1 (p. 112) deduct : For each part of Pb found in No. 3, 0-1550 part. CaO „ „ 4, 0-5715 „ MgO „ „ 4, 0-7944 „ The remainder indicates the sulphur available for the manufac- ture of sulphuric acid. The S of BaSO^, etc., remains in the residue from the dissolving process. P. — Cinders from Blende. 1. Sulphur (according to Lunge and Stierlin, Zsch.f. angew. Chemt, 1906, p. 26). — The process is carried out as described for SULPHURIC ACID MANUFACTURE 115 pyrites cinders on p. Ill, but 2 g. ground potassium chlorate is added to the mixture. The bottom of the crucible should finally be at a red heat, but the contents should merely frit together, not fuse entirely. The crucible must be covered during the heat- ing, and its contents must not be stirred up. The calculation is as on p. 112 — that is, the percentage of S= ^^— . An addition of potassium chlorate is already required in the case of cinders from iron pyrites containing much zinc. In case the cinders contain upwards of 6 per cent. S, the mixture should be : 1-603 g. cinders, 2-000 NaHCOs, 4-0 KCIO3, 2-3 ferric oxide (free from S). The percentage of sulphur is then =11 -6, where a is the c.c. of normal acid corresponding to the 2-000 bicarbonate, 6 the c.c. of acid required for titration after the heating. This process is also applicable to fresh (unroasted) blende, by using the following mixture : 0-3207 g. blende, 2-000 NaHCOs, 2KCIO3, 2Fe203 ; percentage of S = 5 (a - 6). A crude test is made by the foreman at the works, in this manner : he hfeats a sample of the cinders with 10 c.c. hydro- chloric acid (1 : 2 water) m a flask, holding in its neck a strip of paper soaked in a neutral or faintly alkaline solution of lead acetate, and he judges of the more or less complete state of roast- ing by the depth of the brown colour developed on the paper. 2. Zinc, as on p. 110. Gr. — Gases. I. Chamber Process. 1. Burner Gases. — (a) SO2 is estimated by Reich's method. The gas is aspirated through a solution of iodine, contained in a wide-necked 200 c.c. bottle, and coloured blue by starch solution, till the colour is just discharged. This bottle is connected with a larger bottle, converted into an aspirator by having a tap near the bottom, or by a siphon with a pinchcock. Water is run from this into a graduated 250 c.c. jar. The iodine bottle is shaken up during the aspiration, and at the moment when the colour is discharged, the tap of the aspirator is closed and the volume of water in the jar is read off. It is equal to the volume of the water run out, increased by that of the SO2 absorbed. The absorb- ing-bottle is charged with 10 c.c. of a decinormal solution of iodine (12-692 g. iodine per litre, preparation and valuation in the Appendix), along with about 50 c.c. of water, a little starch solu- tion, and a little sodium bicarbonate. The above quantity of iodine is = 0-03207 g. SO2 = 10'95 c.c. at 0° C. and a pressure of 760 mm. The latter figure, multiplied by 100 and divided by 10'95 c.c. -I- the volume of the water run out, yields the percentage of SO2 in the gas by volume. 116 THE TECHNICAL CHEMISTS' HANDBOOK This calculation is saved by the following table, in which the 10'95 c.c. are taken into account. c.c. Water in the Per cent. SO2 c.c Water in the Per cent. 80; Measuring Jar. by Volume. Measuring Jar. by Volume. 80-3 12-0 126-0 8-0 84-3 11-5 135-1 7-5 88-6 11-0 145-5 7-0 93-4 10-5 157-6 6-6 98-6 10-0 171-6 6-0 104-4 9-5 188-2 5-5 110-3 9-0 208-1 5-0 117-9 8-5 In this no notice is taken of temperature and barometer. If these are to be observfed, the volume read off is reduced to 0° and 760 mm. by the Tables 20 and 21, and then looked up in the above table. (6) Since Reich's test takes no account of the SO,, always present in burner gases, it is preferable to estimate the total acids (SO2+SO3), either along with the test (a) or exclusively. This is performed in the same apparatus, but the absorbing- bottle is preferably provided with a gas entrance tube, closed at the bottom and perforated by numerous pinholes, through which the gas issues in small bubbles. The gas is passed through a solution of decinormal sodium hydroxide, coloured by phenol- phthalein, untU the colour is just discharged. The calculation is made as for pure SO2, employing the table given in (a) (Lunge, Zseh.f. angew. Chem., 1890, p. 563). In both cases — (a) and (6) — an error is sometimes caused by arsenions oxide collecting in the aspirating tube ; this is avoided by filtering the gases through asbestos. 2. Chamber Gases. — In these, svlphur dioxide and nitrom gases are estimated (as described by Raschig, Zsch. angew. Chem., 1909, xxii., p. 1182) by means of a Reich apparatus (p. 115), charged with 10 c.c. decinormal iodine solution, '100 c.c. water, a little starch solution, and 10 c.c. of a cold saturated solution of sodium acetate. The estimation is performed as described on p. 115, taking care that no droplets of sulphuric acid get into the iodine solution, which is effected by passing the chamber gases through glass wool. The calculation of SO2 is effected as described supra. In order to estimate the nitrous gases, add, after estimating the SO2, a drop of phenolphthalein solution to the decolorised solution, and titrate with decinormal caustic soda solution up to the appearance of a red colour. From the number of c.c. used deduct 10 c.c. for the hydriodic acid and 10 c.c. for the sulphuric acid formed, according to the equation : S02+J2+2H30 = H2S04+2HJ. The c.c. of decinormal soda SULPHURIC ACID MANUFACTURE 117 solution, used over and above these 20 c.c, indicate nitric or nitrous acid. 3. Chamber Exit Gases. — (a) Oxygen. Before estimating this, the acids are removed from the gas by washing with a solution of potassium or sodium hydroxide. Single samples can be takeu at odd times during the day, but it is recommended to take an average sample for the whole day, by aspirating at least 10 or 20 litres of gas, and analysing a portion of this. The estimation of oxygen is best made by moist phosphorus in an Orsat apparatus (p. 95^ with two absorbing tubes, one of which is filled with potassium hydroxide solution for removing the acids, the other with small pieces of phosphorus. The manipulation is exactly as in testing flue gases, but it should be observed that the tempera- ture must be at least 16°, better 18° C, otherwise the tube must be warmed a little. (b) Sulphur amd Nitnrogen Acids. — The different acid com- pounds of sulphur and nitrogen are estimated together, whatever their degree of oxidation. The following methods agree in the main with those published by the British Alkali Makers' Associa- tion in 1878, but are improved in some analytical details. A con- tinuous test over twenty-four hours is taken of the gases escaping from the exit pipes of the Gay-Lussac towers, aspirating at least one cubic foot per hour by means of any aspirator acting at a constant rate and recording the volume of gas=V by means of gauging the aspirator or by a gas meter. The volume V is reduced to 0° C. and 760 mm. pressure ( = 32° F. and 29-92 inches*) by the Tables 20 and 21, and is called V^. In order to allow comparisons, the number of cubic feet of chamber space per pound of sulphur, burnt and passing into the chambers is recorded, excluding towers, but including tunnels, the amount of sulphur being taken by the weekly average, each firm to state the distance of the testing hole from the point at which the gases leave the Gay-Lussac towers. The absorption apparatus consists of four bottles or tubes, con- taining not less then 100 c.c. of absorbing liquid each, with a depth of at least 3 in. in each bottle, the aperture of inlet tubes not to exceed -^ in. in diameter, and to be measured by a standard wire. The first three bottles each contain 100 c.c. of normal caustic soda solution (Sl'OO g. per litre), the fourth 100 c.c. dis- tilled water. The caustic soda used must be free from nitrogen acids. The gases are tested (1) for total acidity, stated in grains of SO3 per cubic foot of gas, or in grams per cubic metre; (2) sulphur acids ; (3) nitrogen acids, both stated in grains of S and N per cubic foot (or grams per cubic metre). The analysis is carried out as follows : — The contents of the four * The law prescribes the cubic feefc to be measured at 60° F. and 30 inches, which necessitates the use of other tables or factors than those mentioned in the text, but the difference is hardly perceptible, and certainly within the limits of experimental error. 118 THE TECHNICAL CHEMISTS' HANDBOOK bottles are united, taking care not to unnecessarily augment the bulk of the liquids, and are divided into three equal parts,_one of which is reserved for accidents, etc. The first part is titrated with normal sulphuric acid (49'04 g. SO4H2 per litre), to ascertain total acidity. The number of cubic centimetres of acid necessary for neutralisation is called x. The second part of the liquid is gradually poured into a warm solution of potassium permanganate, strongly acidified with pure sulphuric acid. A small excess of permanganate must be present, and must be afterwards reduced by the addition of a few drops of sulphurous acid solution, until only a faint red tint is visible. Now all nitrogen acids are present as HNO3, but no excess of SO2. The HNO3 is estimated by its action on FeS04. Twenty-five c.c. of a solution, containing per litre 100 g. crystallised ferrous sulphate and 100 c.c. pure sulphuric acid (the same solution which is used for estimating MnOj, p. 156) are put into a flask, 20 c.c. to 25 c.c. pure concentrated sulphuric acid is added, the mixture is allowed to cool, and the other mixture, treated with permanganate, etc., is added. The flask is closed by a cork with glass tubes. A current of CO2 passes through and issues beneath the surface of some water, to prevent entrance of air. First, all the air is expelled in this way by means of an apparatus giving a constant current of CO2 ; then the solutions are introduced, and the contents of the flask are heated to boiling, till the dark colour produced by the forma- tion of NO has changed to a clear light yellow. This takes from a quarter of an hour to one hour, according ta the quantity of NO3H, present and that of the sulphuric acid added. The unoxidised ferrous sulphate is titrated by a seminormal perman- ganate solution (yielding 0*004 g. oxygen per cubic centimetre — compare Appendix). _ The cubic centimetre used=iy. Since the titre of the iron solution changes somewhat quickly, it should be tested daily by taking out 25 c.c. with the same pipette as is used for the above operation, and ascertaining the amount of perman- ganate required for oxidising it=z c.c. The data required are found by the following equations : — 1. Tuiai /icidilT/ in grams per 1. Total jlctdtii/ in grains per cubic metre = cubic foot = „„_ 0-120(100-3!) _ 1-852(100-2!) OU3 — :yj &U3 — yl 2. Sulphwr in grams per cubic 2. Sulphur in grains per cubic metre = foot = _ 0-008(600-6j!-z-l-y) - _ 0-12346(600-6a!-z+y) 8. Nitrogen, in grams per cubic 8. Nitrogen in grains per cubic metre = foot = „ _ 0-00 7 (z-y) „ _ 0-10803(z-y) " ~ yi yi SULPHURIC ACID MANUFACTURE 119 The legal limit for total acidity in the lead-chamber process is 4 grains of SO3 per cubic foot, before admixture with air, smoke, or other gases ; for the contact process, the " best practi- cable means " are to be adopted.* For the purposes of the Alkali Act, it is suflScient, in lieu of the above process, to estimate toted acidity only by the test describedon p. 118, employing decinormal soda solution and phenolphthalein. (c) Nitric Oxide (NO) may be present in the exit gases after passing through the absorbing-bottles. If it is to be estimated, an absorption-tube (Fig. 8) t is interposed between the tubes of the apparatus described above and the aspirator. This tube con- c 1 Fig. S. tains 30 c.c. of seminormal permanganate and 1 c.c. of sulphuric acid, specific gravity 1'25. The gas is passed through for twenty- four hours, and the tube then emptied and washed out. Now add 50 c.c. ferrous sulphate solution, corresponding to 2 z perman- ganate (compare last paragraph), and retitrate the decolorised liquid with permanganate. The quantity of the latter now used is called M. The NO has consumed (30-1- m-Ss) c.c. permanganate, which is equal — In grams of nitrogen per cubic In grains of nitrogen per cubic metre of the volume VI. foot. _ 0-007 (30 -t-K- 22) _ 0-10803 (30 -I- m-2z ) II. Contact Process. 1. The Untering Gases are analysed like those of the Chamber Process (p. 115). 2. The Catalysed Gases are passed through a measured quantity of iodine solution, and then through a vessel containing thio- sulphate solution. The non-consumed iodine is retitrated by thiosulphate, and the total acidity is a,scertained by baryta solution or by decinormal soda solution, with phenolphthalein as » Alkali Act, 1906. t This shape of bulb-tubes has been found to be far superior to any other form of absorption-tubes tried. 120 THE TECHNICAL CHEMISTS' HANDBOOK indicator, making the same deduction as prescribed in the Reich- Easchig method (p. 116). If the c.c. of 1/10 iV iodine solution consumed are designated by a, and those of 1/10 TV soda solution (or baryta solution) by 6, the formula a; = 0"003207a indicates the quantity of non-catalysed SO2, and i/=0'004 {b-2a) that of the SO3, formed. The yield of SO3 in volume per cent, is shown by the formula : — (6-2o)100 H. — Sulphuric Acid. 1. Specific Gravity. — The specific gravity tables of sulphuric acid refer, of course, to chemically pure acid. Since, in the case of high-grade acids, the impurities alv^ays present in commercial acids quite sensibly increase the specific gravity, the table in the case of acids over 90 per cent. H2SO4 should only be employed for the private use of the works, but sales should always be effected on the basis of a real analysis, as described later on under No. 9, p. 135. The following table is based on that which the author formerly worked out from a series of very careful investigations, carried on with Isler and Naef ; some corrections introduced by the Imperial German Standards Commission are incorporated. It should be noted that the highest percentages show lower specific gravities than those just below, the maximum being at 99"35 per cent. H2SO4. SULPHURIC ACID MANUFACTURE 121 1. SPBOIFIC GRAVITY OP SULPHURIC ACID AT 60° P. 100 parts by weight 1 Cubic Foot of Acid Speciac Degrees contain Kilo per litie. 60- P. Gravity. Twaddell. 80s. HaS04. HaSOi. Weighs lbs. avoir. Contains lbs. avoir. H2SO4. 1-200 40 22-30 27-32 0-328 74-82 20-44 1-205 • 41 22-82 27-95 0-337 75-14 21-00 1-210 42 23-33 28-58 0-346 75-45 21-57 1-215 43 23-84 29-21 0-355 75-76 22-14 1-220 44 24-36 29-84 0-364 76-07 22-71 1-225 45 24-88 30-48 0-373 76-38 23-28 1-2315 46 25-39 31-11 0-382 76-69 23-85 1-235 47 25-88 31-70 0-391 77-00 24-41 1-240 48 26-35 32-28 0-400 77-32 24-97 1-245 49 26-83 32-86 0-409 77-63 25-54 1-250 50 27-29 33-43 0-418 77-94 26-10 1-255 51 27-76 34-00 0-426 78-25 26-66 1-260 52 28-22 34-57 0-435 78-56 27-23 1-265 53 28-69 35-14 0-444 78-87 27-79 1-270 54 29-15 35-71 0-454 79-19 28-35 1-275 55 29-62 36-29 0-462 79-50 28-92 1-280 66 30-10 36-87 0-472 79-81 29-48 1-285 57 30-57 37-45 0-481 80-12 30-04 1-290 58 31-04 38-03 0-490 80-43 30-60 1-295 59 31-52 38-61 0-500 80-74 31-17 1-300 60 31-99 39-19 0-510 81-06 31-74 1-305 61 32-46 39-77 0-519 81-37 32-32 1-310 62 32-94 40-35 0-529 81-68 32-89 1-315 63 33-41 40-93 0-538 81-99 33-46 1-320 64 33-88 41-50 0-548 82-30 34-03 1-325 65 34-35 42-08 0-657 82-62 34-60 1-330 66 34-80 42-66 ' 0-567 82-93 35-18 1-335 67 35-27 43-20 0-577 83-24 35-79 1-340 68 35-71 43-74 0-586 83-65 36-40 1-345 69 36-14 44-28 0-696 83-86 37-01 1-350 70 36-58 % 44-82 0-605 84-17 37-63 122 THE TECHNICAL CHEMISTS' HANDBOOK SPBOIPIO GRAVITY OP SULPHTTRIO AGIO— Contimied. 100 parts by weight 1 Cubic Foot of Acid contain Kilo per 60' F. Specific Degrees litre. Gravity. Twaddell. Contains SO3. H2SO4. H2SO4. ■ffeigbs lbs. avoir. lbs. avoir. H2SO4. 1-355 71 37-02 45-35 0-614 84-49 38-24 1-360 72 37-45 45-88 0-624 84-80 38-85 1-365 73 37-89 46-41 0-633 85-11 39-46 1-370 74 38-32 46-94 0-643 85-42 40-07 1-375 75 38-75 47-47 0-653 85-73 40-68 1-380 76 39-18 48-00 0-662 86-04 41-29 1-385 77 39-62 48-53 0-672 86-36 41-91 1-390 78 40-05 49-06 0-682 86-67 42-52 1-395 79 40-48 49-59 0-692 86-98 43-13 1-400 80 40-91 50-11 0-702 87-29 43-74 1-405 81 41-33 50-63 0-711 87-60 44-36 1-410 82 41-76 51-15 0-721 87-92 44-97 1-415 83 42-17 51-66 0-730 88-23 45-58 1-420 84 42-57 52-15 0-740 88-54 46-18 1-425 85 42-96 52-63 0-750 88-85 46-78 1-430 86 43-36 53-11 0-759 "89-16 47-38 1-435 87 43-75 53-59 0-769 89-47 47-99 1-440 88 44-14 54-07 0-779 89-79 48-59 1-445 89 44-53 54-55 0-789 90-10 49-19 1-450 90 44-92 55-03 0-798 90-41 49-79 1-455 91 45-31 65-50 0-808 90-72 50-39 1-460 92 45-69 55-97 0-817 91-03 50-99 1-465 93 46-07 56-43 0-827 91-35 51-59 1-470 94 46-45 56-90 0-837 91-66 52-19 1-475 95 46-83 57-37 0-846 91-97 52-79 1-480 96 47-21 57-83 0-856 92-28 53-39 1-485 97 47-57 58-28 0-866 92-59 64-00 1-490 98 47-95 58-74 0-876 92-90 64-60 1-495 99 48-34 •59-22 0-886 93-22 65-20 1-500 100 48-73 59-70 0-896 93-53 55-84 1-505 101 49-12 60-18 0-906 93-84 56-47 1-510 102 49-51 60-65 0-916 94-15 57-10 SULPHURIC ACID MANUFACTURE 123 SPBOIPIO GRAVITY OF SULPHURIC ACID— Oontinmd. 100 parts by weight 1 Cubic Foot of Acid Degrees contain Kilo per litre. 00- F. Specific Gravity. TwaddeU. rjnntains SO3. H2SO4. HaS04. Weigbs lbs. avoir. lbs. avoir. H2SO4. 1-515 103 49-89 61-12 0-926 94-46 57-73 1-520 104 50-28 61-59 0-936 94-77 58-36 1-525 105 50-66 62-06 0-946 95-09 59-00 1'530 106 51-04 62-53 0-957 95-40 59-62 1-535 107 51-43 63-00 0-967 95-71 60-26 1-540 108 51-78 63-43 0-977 96-02 60-89 1-545 109 52-12 63-85 0-987 96-33 61-52 1-550 110 52-46 64-26 0-996 96-65 62-15 1-555 111 52-79 64-67 1-006 96-96 62-78 1-560 112 53-22 65-20 1-017 97-27 63-49 1-565 113 53-59 65-65 1-027 97-58 64-10 1-570 114 53-95 66-09 1-038 97-89 64-79 1-575 115 54-32 66-53 1-048 98-20 65-42 1-580 116 54-65 66-95 1-058 98-52 66-04 1-585 117 55-03 67-40 1-068 98-83 66-67 1-590 118 55-37 67-83 1-078 99-14 67-77 1-595 119 55-73 68-26 1-089 99-45 67-96 1-600 120 56-09 68-70 1-099 99-76 68-60 1-605 121 56-44 69-13 1-110 100-07 69-29 1-610 122 56-79 69-56 1-120 100-39 69-92 1-615 123 57-15 70-00 1-131 100-70 70-60 1-620 124 57-49 70-42 1-141 101-01 71-20 1-625 125 57-84 70-85 1-151 101-32 71-85 1-630 126 58-18 71-27 1-162 101-64 72-54 1-635 127 58-53 71-70 1-172 101-95 73-16 1-640 128 58-88 72-12 1-182 102-26 73-79 1-645 129 59-22 72-55 1-193 102-57 74-47 1-650 130 59-67 72-96 1-204 102-88 75-16 1-655 131 59-92 73-40 1-215 103-19 75-84 1-660 132 60-26 73-81 1-225 103-50 76-47 1-665 133 60-60 74-24 1-236 103-82 77-16 124 THE TECHNICAL CHEMISTS' HANDBOOK SPBCIFIO GRAVITY OF SULPHURIC ACID—ContimMd. Specific Gravity. Degrees Twaddell. 100 parts by weight contain Kilo per litre. HjS04. 1 Cubic Foot of Acid 60' F. SO3. H2SO4. Weiglis lbs. avoir. Contains lbs. avoir. H2SO4. 1-670 1-675 134 135 60-95 61-29 74-66 75-08 1-246 1-259 104-13 104-44 77-78 78-59 1-680 1-685 1-690 1-695 1-700 136 137 138 139 140 61-63 61-93 62-29 62-64 63-00 75-50 75-86 76-30 76-73 77-17 1-268 1-278 1-289 1-301 1-312 104-75 105-07 105-38 105-69 106-00 79-16 80-12 80-81 81-51 82-21 1-705 1-710 1-715 . 1-720 1-725 141 142 143 144 145 63-35 63-70 64-07 64-43 64-78 77-60 78-04 78-48 78-92 79-36 1-323 1-334 1-346 1-357 1-369 106-31 106-62 106-94 107-25 107-56 82-90 83-60 84-29 84-99 85-69 1-730 1-735 1-740 1-745 1-750 146 147 148 149 150 65-14 65-50 65-86 66-22 66-58 79-80 80-24 80-68 81-12 81-56 1-381 1-392 1-404 1-416 1-427 107-87 108-18 108-49 108-80 109-12 86-38 87-08 87-77 88-47 89-17 1-755 1-760 1-765 1-770 1-775 151 152 153 154 155 66-94 67-30 67-76 68-17 68-60 ^ 82-00 82-44 83-01 83-41 84-02 1-439 1-451 1-465 1-478 1-491 109-43 109-74 110-05 110-36 110-68 89-86 90-56 91-45 92-26 93-07 1-780 1-785 1-790 1-795 1-800 156 157 158 159 160 68-98 69-47 69-96 70-45 70-96 84-50 85-10 85-70 86-30 86-92 1-504 1-519 1-534 1-549 1-565 110-99 111-30 111-61 111-92 112-23 93-81 94-74 95-67 96-60 97-69 1-805 1-810 1-815 161 162 163 71-50 • 72-08 72-69 87-60 88-30 89-05 1-581 1-598 1-621 112-67 112-98 113-29 98-69 99-75 101-19 SULPHURIC ACID MANUFACTURE 125 SPBOIPIO GRAVITY OP SULPHURIC ACID— Continued. 100 parts by weight 1 Cubic Foot of Acid contain Kilo per 60° F. Speoiflo Degrees litre. Gravity. Twaddell. SO3. H2SO4. H2SO4. Weighs lbs. avoir. Contains lbs. avoir. HaS04. 1-820 164 73-51 90-05 1-639 113-61 102-31 1-821 73-63 90-20 1-643 113-67 102-56 1-822 ... 73-80 90-40 1-647 113-73 102-89 1-823 ... 73-96 90-60 1-661 113-80 103-06 1-824 ... 74-12 90-80 1-656 113-85 103-38 1-825 165 74-29 91-00 1-661 113-92 103-68 1-826 ... 74-49 91-25 1-666 113-99 104-00 1-827 ... 74-69 91-50 1-671 114-04 104-31 1-828 74-86 91-70 1-676 114-11 104-62 1-829 75-03 91-90 1-681 114-19 104-93 1-830 166 75-19 92-10 1-685 114-23 105-18 1-831 75-46 92-43 1-692 114-30 105-62 1-832 75-69 92-70 1-698 114-36 105-99 1-833 75-89 92-97 1-704 114-42 106-38 1-834 76-12 93-25 1-710 114-47 106-74 1-835 167 76-35 93-56 1-717 114-54 107-43 1-836 76-57 93-80 1-722 114-61 107-49 1-837 76-90 94-20 1-730 114-67 107-99 1-838 77-23 94-60 1-739 114-73 108-55 1-839 77-55 95-00 1-748 114-80 109-12 1-840 168 78-04 95-60 1-759 114-86 109-80 1-8405 78-33 95-95 1-765 114-89 110-18 1-8410 78-69 96-30 1-784 114-92 110-73 1-8415 79-47 97-35 1-792 114-95 111-86 1-8410 80-16 98-20 1-808 114-92 112-86 1-8405 80-43 98-52 1-814 114-89 113-23 1-8400 80-59 98-72 1-816 114-86 113-36 1-8395 80-63 98-77 1-817 114-83 113-48 1-8390 80-93 99-12 1-823 114-80 113-80 1-8385 81-08 99-31 1-826 114-76 113-98 126 THE TECHNICAL CHEMISTS* HANDBOOK 2. TABLE FOB REDUCING THE SPBOIPIO GRAVITIES OP SULPHURIC ACID OP VARIOUS STRENGTHS TO ANY OTHER TEMPERATURE (DEGREES C). 0°. 5°. 10°. 15°. 20°. 25°. 30°. 35°. 40°. 45°. 50°. 1-857 1-852 1-846 1-840 1-836 1-830 1-825 1-821 1-816 1-811 1-806 1-847 1-841 1-836 1-830 1-825 1-820 1-815 1-810 1-805 1-800 1-796 1-887 1-831 1-825 1-820 1-815 1-809 1-804 1-799 1-794 1-789 1-784 1-827 1-821 1-815 1-810 1-805 1-799 1-793 1-788 1-783 1-778 1-773 1-817 1-811 1-805 1-800 1-794 1-788 1-783 1-777 1-772 1-766 1-V61 1-807 1-801 1-796 1-790 1-784 1-778 1-773 1-767 1-762 1-756 1-761 1-797 1-791 1-786 1-780 1-774 1-768 1-763 1-767 1-762 1-746 1-741 1-786 1-781 1-776 1-770 1-765 1-759 1-764 1-748 1-743 1-737 1-732 1-776 1-770 1-766 1-760 1-755 1-749 1-744 1-738 1-733 1-728 1-723 1-765 1-760 1-755 1-750 1-745 1-740 1-736 1-730 1-726 1-720 1-715 1-754 1-760 1-745 1-740 1-735 1-730 1-726 1-721 1-716 1-711 1-706 1-744 1-740 1-735 1-730 1-726 1-720 1-716 1-711 1-706 1-701 1-696 1-734 1-730 1-725 1-720 1-715 1-710 1-706 1-701 1-696 1-691 1-686 1-724 1-720 1-715 1-710 1-705 1-700 1-696 1-691 1-686 1-681 1-676 1-714 1-710 1-705 1-700 1-695 1-690 1-686 1-681 1-676 1-671 1-667 1-704 1-roo 1-695 1-690 1-685 1-680 1-676 1-671 1-666 r661 1-666 1-694 1-690 1-685 1-680 1-676 1-670 1-666 1-661 1-656 1-651 1-646 1-684 1-680 1-675 1-670 1-665 1-660 1-656 1-661 1-646 1-641 1-637 1-674 1-670 1-665 1-660 1-655 1-650 1-646 1-641 1-636 1-632 1-628 1-664 1-660 1-656 1-660 1-645 1-640 1-636 1-632 1-627 1-622 1-618 1-654 1-650 1-645 1-640 1-635 1-631 1-626 1-622 1-617 1-612 1-608 1-644 1-640 1-635 1-630 1-626 1-621 1-616 1-612 1-607 1-602 1-698 1-634 1-630 1-625 1-620 1-615 1-611 1-606 1-602 1-597 1-592 1-588 1-624 1-620 1-616 1-610 1-605 1-601 1-696 1-592 1-587 1-682 1-678 1-614 1-610 1-605 1-600 1-595 1-591 1-686 1-582 1-577 1-572 1-668 1-604 1-600 1-596 1-590 1-586 1-581 1-676 1-672 1-567 1-562 1-558 1-594 1-589 1-584 1-680 1-575 1-670 1-566 1-562 1-558 1-553 1-548 1-684 1-579 1-574 1-570 1-666 1-561 1-556 1-662 1-548 1-643 1-539 1-674 1-669 1-564 1-660 1-656 1-562 1-547 1-543 1-539 1-534 1-630 1-563 1-668 1-554. 1-550 1-546 1-642 1-638 1-534 1-630 1-525 1-521 1-652 1-548 1-644 1-540 1-586 1-532 1-628 1-624 1-520 1-616 1-612 1-542 1-538 1-534 1-630 1-526 .1-622 1-618 1-614 1-510 1-506 1-502 1-532 1-528 1-624 1-620 1-516 1-512 1-508 1-604 1-500 1-497 1-492 1-622 1-518 1-614 1-510 1-506 1-502 1-498 1-494 1-490 1-486 1-482 1-512 1-608 1-604 1-500 1-496 1-492 1-488 1-484 1-480 1-476 1-472 1-502 1-498 1-494 1-490 1-486 1-482 1-478 1-474 1-470 1-466 1-462 1-492 1-488 1-484 1-480 1-476 1-472 1-468 1-465 1-461 1-467 1-453 1-482 1-478 1-474 1-470 1-466 1-462 1-458 1-455 1-451 1-447 1-443 1-472 1-468 1-464 1-460 1-456 1-452 1-448 1-445 1-442 1-438 1-434 1-462 1-468 1-454 1-460 1-446 1-442 1-438 1-436 1-432 1-429 1-426 1-452 1-448 1-444 1-440 1-436 1-432 1-429 1-426 1-423 1-420 1-416 1-442 1-438 1-434 1-430 1-426 1-422 1-419 1-416 1-413 1-409 1-405 1-432 1-428 1-424 1-420 1-416 1-413 1-410 1-406 1-402 1-398 1-394 1-422 1-418 1-414 1-410 1-406 1-403 1-399 1-396 1-392 1-388 1-384 1-412 1-408 1-404 1-400 1-396 1-398 1-389 1-386 1-382 1-378 1-37* 1-402 1-398 1-394 1-390 1-886 1-388 1-879 1-372 1-372 1-868 1-364 1-392 1-388 1-884 1-380 1-876 1-378 1-370 1-362 1-362 1-359 1-865 1-382 1-378 1-874 1-370 1-366 1-368 1-360 1-852 1-362 1-349 1-346 1-872 1-368 1-864 1-360 1-866 1-858 1-850 1-844 1-344 1-840 1-336 1-362 1-368 1-354 1-350 1-346 1-343 1-340 1-334 1-334 1-330 1-326 SULPHURIC ACID MANUFACTURE TABIiE 2 — Continmed. 12'! 6B'. 60'. 65'. 70°. 75°. 80°. 85°. 90°. 95°. 100°. 1-801 1-796 1-792 1-787 1-782 1-778 1-774 1-770 1-766 1-762 1-790 1-787 1-781 1-776 1-770 1-766 1-762 1-767 1-762 1-748 1-779 1-774 1-769 1-764 1-769 1-764 1-740 1-744 1-789 1-734 1-767 1-762 1-757 1-762 1-747 1-741 1-786 1-781 1-726 1-721 1-765 1-760 1-744 1-739 1-734 1-729 1-724 1-719 1-714 1-708 1-746 1-741 1-785 1-780 1-726 1-720 1-715 1-710 1-706 1-700 1-786 1-731 1-726 1-721 1-716 1-712 1-707 1-702 1-697 1-692 1-727 1-722 1-717 1-712 1-707 1-702 1-697 1-698 1-688 1-683 1-718 1-713 1-708 1-703 1-698 1-693 1-688 1-684 1-679 1-674 1-710 1-706 1-700 1-696 1-699 1-686 1-681 1-676 1-671 1-667 1-702 1-697 1-692 1-688 1-683 1-678 1-674 1-669 1-664 1-660 1-692 1-687 1-688 1-678 1-673 1-668 1-664 1-669 1-664 1-660 1-682 1-677 1-678 1-668 1-668 1-669 1-664 1-649 1-644 1-640 1-672 1-667 1-663 1-668 1-658 1-649 1-644 1-639 1-636 1-630 1-662 1-667 1-668 1-648 1-644 1-689 1-634 1-680 1-625 1-620 1-662 1-647 1-642 1-638 1-634 1-630 1-625 1-620 1-615 1-610 1-642 1-687 1-632 1-628 1-624 1-620 1-615 1-611 1-606 1-602 1-633 1-628 1-623 1-619 1-615 1-611 1-606 1-602 1-697 1-693 1-623 1-619 1-614 1-610 1-606 1-602 1-597 1-698 1-688 1-684 1-614 1-610 1-606 1-600 1-596 1-692 1-688 1-6S3 1-679 1-676 1-604 1-600 1-595 1-591 1-686 1-682 1-578 1-674 1-670 1-566 1-694 1-590 1-686 1-681 1-677 1-573 1-569 1-666 1-561 1-566 1-684 1-680 1-576 1-572 1-668 1-564 1-560 1-556 1-662 1-547 1-674 1-670 1-566 1-662 1-558 1-554 1-560 1-546 1-642 1-637 1-664 1-600 1-566 1-652 1-648 1-544 1-540 1-636 1-631 1-527 1-664 1-650 1-545 1-641 1-637 1-633 1-629 1-626 1-521 1-616 1-544 1-639 1-635 1-531 1-527 1-628 1-619 1-515 1-610 1-606 1-635 1-631 1-626 1-522 1-618 1-518 1-609 1-606 1-601 1-496 1-626 1-522 1-617 1-513 1-509 1-604 1-600 1-490 1-492 1-487 1-617 1-513 1-509 1-604 1-500 1-496 1-491 1-487 1-483 1-478 1-508 1-604 1-600 1-496 1'491 1-486 1-482 1-478 1-473 1-469 1-49S 1-494 1-490 1-485 1-481 1-476 1-472 1-468 1-463 1-469 1-488 1-484 1-480 1-476 1-472 1-467 1-462 1-468 1-453 1-449 1-478 1-474 1470 1-466 1-462 1-467 1-452 1-448 1-443 1-438 1-468 1-464 1-460 1-465 1-461 1-446 1-442 1-438 1-433 1-428 1-458 1-454 1-460 1-442 l-44l' 1-437 1-433 1-429 1-424 1-419 1-449 1-445 1-441 1-436 1-432 1-428 1-424 1-419 1-414 1-410 1-439 1-485 1-431 1-427 1-423 1-418 1-414 1-409 1-405 1-401 1-430 1-426 1-422 1-418 1-418 1-409 1-405 1-400 1-396 1-392 1-421 1-417 1-413 . 1-409 1-404 1-400 1-396 1-391 1-387 1-883 1-412 1-407 1-403 1-899 1-395 1-391 1-386 1-382 1-878 1-374 1-401 1-397 1-393 1-389 1-886 1-380 1-876 1-872 1-868 1-364 1-390 1-886 1-882 1-378 1-874 1-370 1-366 1-362 1-858 1-368 1-380 1-876 1-372 1-368 1-364 1-860 1-366 1-852 1-848 1-343 1-370 1-366 1-862 1-358 1-364. 1-360 1-346 1-842 1-838 1-838 1-360 1-856 1-362 1-848 1-851 1-346 1-342 1-388 1-342 1-837 1-384 1-329 1-832 1-827 1-823 1-819 ,, 1-322 1-817 1-814 1-810 128 THE TECHNICAL CHEMISTS' HANDBOOK TABIiEi 2 — Continued. 0°. 6'. 10% 15". 20°. 25°. 30° 35°. 40° 45°. 60'. 1-352 1-348 1-344 1-340 1-336 1-333 1-330 1-327 1-324 1-820 1-316 1-341 1-337 1-333 1-330 1-327 1-324 1-321 1-818 1-314 1-310 1-306 1-330 1-326 1-323 1-320 1-317 1-314 1-311 1-308 1-304 1-801 1-297 1-320 1-316 1-313 1-310 1-307 1-304 1-801 1-298 1-294 1-291 1-287 1-310 l-306r 1-303 1-300 1-297 1-294 1-291 1-288 1-284 1-281 1-277 1-300 1-296 1-293 1-290 1-287 1-284 1-280 1-277 1-274 1-270 1-267 1-290 1-286 1-283 1-280 1-277 1-274 1-270 1-267 1-264 1-260 1-256 1-2S0 1-276 1-273 1-270 1-267 1-264 1-260 1-257 1-254 1-250 1-246 1-270 1-266 1-263 1-260 1-257 1-254 1-251 1-248 1-245 1-241 1-237 1-260 1-256 1-253 1-250 1-247 1-244 1-241 1-238 1-235 1-231 1-227 1-250 1-246 1-243 1-240 1-237 1-234 1-230 1-227 1-224 1-220 1-217 1-240 1-236 1-233 1-230 1-227 1-224 1-220 1-217 1-214 1-210 1-207 1-230 1-226 1-223 1-220 1-217 1-214 V210 1-207 1-204 1-200 1-197 1-220 1-216 1-213 1-210 1-206 1-204 1-200 1-197 1-194 1-190 1-187 1-210 1-206 1-203 1-200 1-196 1-193 1-190 1-186 1-183 1-180 1-176 1-200 1-196 1-193 1-190 1-186 1-183 1-180 1-176 1-173 1-169 1-165 1-190 1-186 1-183 1-180 1-176 1-173 1-170 1-166 1-163 1-159 1-155 1-180 1-176 1-173 1-170 1-166 1-163 1-160 1-156 1-153 1-149 1-146 1-169 1-166 1-163 1-160 1-157 1-163 1-150 1-147 1-144 1-141 1-138 1-159 1-166 1-153 1-150 1-147 1-14S 1-140 1-137 1-134 1-131 1-128 1-149 1-146 1-143 1-140 1-137 1-134 1-131 1-128 1-126 1-122 1-119 1-138 1-135 1-133 1-130 1-127 1-125 1-122 1-119 1-116 1-llS 1-110 1-128 1-125 1-123 1-120 1-118 1-115 1-112 1-110 1-107 1-104 1-102 1-118 1-115 1-118 1-110 1-108 1-105 1-102 1-100 1-097 1-094 1-092 1-lOS 1-105 1-103 1-100 1-097 1-094 1-092 1-090 1-087 1-084 1-082 1-098 1-096 1-093 1-090 1-087 1-084 1-082 1-080 1-077 1-074 1-072 1-088 1-085 1-0S3 1-OSO 1-077 1-074 1-072 1-070 1-067 1-064 1-062 1-078 1-075 1-073 1-070 1-067 1-064 1-062 1-060 1-057 1-054 1-052 1-OOS 1-065 1-063 1-060 1-057 1-064 1-062 1-050 1-048 1-044 1-042 1-068 1-055 1-053 1-050 1-047 1-044 1-042 1-040 1-038 1-034 1-032 1048 1045 1-043 1-040 1-037 1-034 1-032 1-030 1-028 1-024 1-022 1-038 1035 1-033 1-030 1-027 1-024 1-022 1-020 1-018 1-014 1-012 1-02S I 025 1023 1-020 1-017 1-014 1-012 1-010 1-008 1-004 1-002 1-018 1-015 1-018 1-010 1-007 1-004 1-002 1-000 0-998 0-994 0-992 SULPHURIC ACID MANUFACTURE TABIiB 2 — Continued. 129 66°. 60°. 66°. 70°. 75°. 80". 86°. 90°. 95°. 100°. 1-312 1-S08 1-304 1-300 1-302 1-298 1-294 1-290 1-293 1-280 1-284 1-280 1-283 1-279 1-274 1-270 1-273 1-269 1-266 1-260 1-268 1-269 1-256 1-260 1-262 1-243 1-244 1-240 1-242 1-238 1-284 1-230 1-233 1-224 1-224 1-220 1-223 1-214 1-214 1-210 1-210 1-209 1-204 1-200 1-204 1-200 1-196 1-190 1-lM 1-190 1-185 1-180 1-183 1-179 1-175 1-170 1-172 1-168 1-164 1-160 1-162 1-168 1-154 1-160 1-152 1-148 1-144 1-140 1-143 1-139 1-136 1-131 1-136 1-131 1-127 1-123 1-125 1-122 . 1-118 1-114 1-116 1-113 1-109 1-106 1-107 1-104 1-100 1-097 1-099 1-096 1-092 1-OSS 1-089 1-086 1-082 1-078 1-079 1-076 1-072 1-068 1-069 1-065 1-062 1-058 1-069 1-056 1-062 1-048 1-049 1-046 1-042 1-038 1-036 1-086 1-032 1-028 1-039 1-025 1-022 1-018 1-019 ■ 1-015 1-012 1-008 1-009 1-005 1-002 0-998 ;; 0-999 0-995 0-992 0-988 . 0-989 0-985 0-982 0-978 130 THE TECHNICAL CHEMISTS' HANDBOOK S. SPBCIPIC GRAVITIES OP COMMERCIAL (NORDHATTSEN) OIL OP VITRIOL. (Messel, Joum. Soc. Chem. Ind., 1885, p. 573.) Specimens. Percentage ofSOs. Specific Gravity At SO" F. = 26-ti° 0. At 60° P. = 15-6°C. Liquid Crystalline nnass, resembling nitre . Do. do. Do. do. Liquid Do. Do. Crystallised Do. Do. 30-0 40-0 44-5 46-2 59-4 60-8 6.5-0 69-4 V2-8 80-0 82-0 ■842 •930 •956 •961 •963 •980 •992 •992 •002 •984 •959 •953 1-852 1-940 1-970 1-975 1^977 1^994 2^006 2^006 2^016 1^988 1^973 1-967 SULPHURIC ACID MANUFACTURE 131 4. SPBCIPIO GRAVITIES AND PBROBNTAGK OP FUMING (NORDHAUSBN) OIL OP VITRIOL AT DIPPBRBNT TBMPBRATURBS. Density at SO3 Per Cent. 15*. 20% 26-. SO". S5". 1-8417 1-8371 1-8323 1-8287 1 -8240 76-67 1-8427 1-8378 1-8333 1 -8295 1-8249 77-49 1-8428 1-8388 1-8351 1 -8302 1-8255 78-34 1-8437 1-8390 1-8346 1-8300 1-8257 79-04 1-8427 1-8386 1-8351 1-8297 1-8250 79-99 1-8420 1 -8372 1-8326 1-8281 1-8234 80-46 1-8398 1-8350 1-8305 1-8263 1-8218 80-94 1-8446 1-8400 1-8353 1-8307 1-8262 81-37 1-8509 1-8466 1-8418 1-8371 1-8324 81-91 1-8571 1-8522 1-8476 1-8432 1-8385 82-17 1-8697 1-8647 1-8595 1-8545 1-8498 82-94 1-8790 1-8742 1-8687 1-8640 1-8592 83-25 1-8875 1-8823 1-8767 1-8713 1-8661 83-84 1-8942 1-8888 1-8833 1-8775 1-8722 84-12 1-8990 1-8940 1-8890 1-8830 1-8772 84-33 1-9034 1-8984 1-8930 1-8874 1 -8820 84-67 1-9072 1-9021 1-8950 1-8900 1-8845 84-82 1-9095 1-9042 1-8986 1-8932 1-8866 84-99 1-9121 1-9053 1-8993 1 -8948 1-8892 85-14 1-9250 1-9193, 1-9135 1-9082 1-9028 85-54 1-9290 1-9236 1-9183 1-9129 1-9073 85-68 1-9368 1-9310 1-9250 1-9187 1-9122 85-88 1-9447 1-9392 1-9334 1-9279 1-9222 86-51 1-9520 1-9465 1-9402 1-9338 1 -9278 86-72 1-9584 1-9528 1-9466 1-9406 1-9340 87-03 1-9632 1-9573 1-9518 1-9457 1-9398 87-46 cryst. cryst. 1-9740 1-9666 1-9740 88-00 The above table Is only intended for control in works, but not for commercial purposes, because the specific gravity is anything but a certain guide for the percentage of Nordhausen acid, and altogether fails as such, for strengths just below the monohydrate. The table was not made for chemically pure acids, but for commercial acid. 132 THE TECHNICAL CHEMISTS' HANDBOOK 5. FREEZING AND MELTING POINTS OP SULPHURIC ACID.* Specific Gravity at 16'. Freezing Point. Melting Point. 1-671 Liquid at -20° 1-691 Liquid at -20° ... 1-712 Liquid at - 20° 1-727 -7-5° -7-5° 1-732 -8-5° -8-5° 1-749 -0-2° + 4-5° 1-767 + 1-6° + 6-5° 1-778 + 8-5° + 8-5° 1-790 + 4-5° + 8-0° 1-807 -9-0° -6-0° 1-822 Liquid at -20° 1-840 Liquid at -20° * Lunge, Benclite d. dmtsch. cAero. Ges., 1881, s. 2649. 6. BOILING POINTS OF SULPHURIC ACID. (Lunge, Ber. d. d. chem. Ges., 11, 370.) Per Cent. SO4H2. Specific Boiling Per Cent. SO4H2. Specific Boiling Per Cent. SO4H2. Specific Boiling Gravity. Point. Gravity. Point. Gravity. Point. Degrees. Degrees. Degrees. 5 1-031 101 56 1-459 133 82 1-758 218-5 10 1-069 102 60 1-503 141-5 84 1-773 227 15 1-107 103-5 62-5 1-530 147 86 1-791 238-5 20 1-147 105 65 1-557 153-5 88 1-807 251-5 25 1-184 106-5 67-5 1-585 161 90 1-818 262-5 30 1-224 108 70 1-615 170 91 1-824 268 35 1-265 110 72 1-639 174-5 92 1-830 274-5 40 1-307 114 74 1-661 180-5 93 1-834 281-5 45 1-352 118-5 76 1-688 189 94 1-837 288-5 50 1-399 124 78 1-710 199 95 1-840 295 53 1-428 128-5 80 1-733 207 Monohydrate (100 per cent.) boils at 338° (Marignac). SULPHURIC ACID MANUFACTURE 133 7. FUSING POINTS* OP SULPHURIC ACID AND OP NORDHAUSBN OIL OP VITRIOL. (KNIBTSOH.) Sulphur ic Acid. Nordhauaen Oil of Vitriol. Percentage ofSOa (as H2S64). Fusing Point. Percentage of SO.) Fusing Point. Percentage of Fusing Point. •c. (as H2Sb4). °C. free SO3. ■c. Per cent. Per cent. Per cent. 1 SO3 - 0-6 69 SO3 + 7-0 SO3 + 10-0 2 „ - 1-0 70 „ + 4-0 5 „ + 3-5 3 „ - 1-7 71 „ - 1-0 10 „ - 4-8 4 „ - 2-0 72 „ - 2-0 15 „ -11-2 5 „ - 2-7 73 „ -16-2 20 „ -11-0 6 „ - 3-6 74 „ -25-0 25 „ - 0-6 7 „ - 4-4 75 „ -34-0 30 „ + 15-2 8 ,, - 5-3 ?«166° 78 J E^ -32-0 35 „ + 26-0 9 ,. - 6-0 -33-0 40 „ + 33-8 10 „ - 6-7 -16-5 45 „ + 34-8 11 „ - 7-2 79 „ - 5-2 50 „ + 28-5 12 „ - 7-9 80 „ + 3-0 55 „ + 18-4 ■ 13 „ - 8-2 81 „ + 7-0 60 „ + 0-7 14 „ - 9-0 82 „ + 8-2 65 „ + 0-8 15 „ - 9-3 83 „ - 0-8 70 „ + 9-0 16 „ - 9-8 84 „ - 9-2 75 „ + 17-2 17 „ -11-4 85 „ -11-0 80 „ + 22-0 18 „ -13-2 86 „ - 2-2 85 „ + 33-0 (27 )t 19 „ -15-2 87 „ + 13-5 90 „ + 34-0(2.^) 20 „ -17-1 88 „ + 26-0 95 „ + 36-0 ( 6) 21 „ -22-5 89 „ + 34-2 100 „ + 40-0(15) 22 „ -31-0 90 „ + 34-2 23 „ -40-1 91 „ + 25-8 ::: ;: } below 92 „ + 14-2 -40 93 „ + 0-8 61 „ -40-0 94 „ + 4-5 62 „ -20-0 95 „ + 14-8 63"! 60° 64/ B^ -11-5 96 „ + 20-3 - 4-8 97 „ + 29-2 65 „ - 4-2 98 „ + 33-8 66 „ + 1-2 99 ,, + 36-0 67\ 62° 68/ B^ + 8-0 100 „ + 40-0 + 8-0 * " Fusing Poiut " is understood to be the temperature to which the mercury of the thermometer, dipping into the solidifying liquid, rises and at which it remains constant. It should be noticed that la/rge quantities of Nordhausen oil of vitriol, such as exist in transportation vessels, frequently do not behave in accord with the above data, because during the carriage and storage a separation often takes place in the acid, crystals of a different concentration being formed, which of course possess a correspondingly different fusing point. t The figures in parentheses signify the fasing points of freshly made Nordhausen oil of vitriol, which has not polymerised. 134 THE TECHNICAL CHEMISTS' HANDBOOK 8. PERCENTAGE OP SO3 IN NORDHAUSEN OIL OF VITRIOL. (GNEHM.) Found by Contains per Found by Contains per Found by Contains per cent ■ Titrating. SO3. en Titrating. SO3. Titrating. SO3. SO4H2. SOs. SO4H2. SO3. SO4H2. SO3 81-6326 100 87-8775 66 34 93-9387 33 67 81-8163 99 1 88-0612 65 35 94-1224 32 68 82-0000 98 2 88-2448 64 36 94-3061 31 69 82-1836 97 3 88-4285 63 37 94-4897 30 70 82-3674 96 4 88-6122 62 38 94-6734 29 71 82-5510 95 5 88-7959 61 39 94-8571 28 72 82-7346 94 6 88-9795 60 40 95-0408 27 73 82-9183 93 7 89-1632 59 41 95-2244 26 74 83-1020 92 8 89-3469 58 42 95-4081 25 • •• 83-2857 91 9 89-5306 57 43 95-5918 24 83-4693 90 10 89-7142 56 44 95-7755 23 83-6530 89 11 89-8979 55 45 95-9591 22 83-8367 88 12 90-0816 54 46 96-1428 21 84-0204 87 13 90-2653 53 47 96-3265 20 84-2040 86 14 90-4489 52 48 96-6102 19 84-3877 85 15 90-6326 51 49 96-6938 18 84-5714 84 16 90-8163 50 50 96-8775 17 84-7551 83 17 91-0000 49 51 97-0612 16 84-9387 82 18 91-1836 48 52 97-2448 15 85-1224 81 19 91-3673 47 53 97-4285 14 85-3061 SO 20 91-5510 46 54 97-6122 13 85-4897 79 21 91-7346 45 55 97-7959 12 85-6734 78 22 91-9183 44 56 97-9795 11 85-8571 77 23 92-1020 43 57 98-1632 10 86-0408 76 24 92-2857 42 58 98-3469 9 86-2244 75 25 92-4093 41 59 98-5306 8 86-4081 74 26 92-6530 40 60 98-7142 7 86-5918 73 27 92-8367 39 61 98-8979 6 86-7755 72 28 93-0204 38 62 99-0816 5 86-9591 71 29 93-2040 37 63 99-2653 4 87-1428 70 30 93-3877 36 64 99-4489 3 87-3265 69 •31 93-5714 35 65 99-6326 2 .« 87-5102 68 32 93-7551 34 66 99-8163 1 i-fc. 87-6938 67 33 SULPHURIC ACID MANUFACTURE 135 9. The Quantitative Examination of Free Sulphuric Acid. The quantitative examination of free sulphuric acid is made by titrating a weighed quantity. It is not suflSciently accurate to measure the acid by a pipette, etc., especially in the case of concentrated acid. The titration is performed by means of standard sodium hydroxide solution, and the results are expressed in terms of H2SO4. Weigh from 2 to 3 g. acid in a glass-tap pipette (Fig. 12, p. 145), after cleaning the latter on the outside ; run its contents into at least 100 c.c. water, and weigh the pipette again, without washing it out. This enables another pipette full of acid to be taken and tested, without washing and drying the instrument, and so forth. The same procedure is also very well adapted for slightly fuming mixtures of sulphuric and nitric acid, and for Nordhausen oil of vitriol {cf. p. 145). The standard sodium hydroxide solution is " normal," i.e. con- taining 004001 NaOH g. per litre. It is controlled by means of standard hydrochloric acid (0'03647 g. HCl per litre), the strength of which has been fixed by pure sodium carbonate. The method is described in detail in the Appendix. As indicator, methyl orange is used always in the cold, and so much only is taken that the colour produced is just visible. Nitrous acid destroys this colouring matter, but ordinary com- mercial acid never contains sufficient to cause any trouble, and even " nitrous vitriol " or fuming nitric acid can be treated with methyl orange, if the indicator is added (or renewed) shortly before the last quantity of alkali has been added ; or else an excess of alkali is added, then methyl orange, and titrated back. Nitrous acid behaves towards methyl orange like the strong mineral acids ■ that is, the change of colour takes place when the compound NaN02 has been formed. 10. Examination of Sulphuric Acid for other Substances. (a) Nitrous Add (Nitrososulphuric Acid) is titrated with seminormal permanganate. (Preparation in the Appendix.) This can be done without loss of NO by manipulating as follows (Lunge, Berliner Berichte, x., 1075) : — Put the nitrous vitriol into a burette fitted with a glass tap, run it slowly into a measured quantity of permanganate, diluted with five times its volume of tepid water (30° C. to 40° C.), and agitate continuously -136 THE TECHNICAL CHEMISTS" HANDBOOK till the colour just vanishes. Sometimes during this process a little manganese dioxide is separated, which makes it difiScult to recognise the end of the reaction, but this is avoided by keeping TABIiB FOR ESTIMATING NITROUS VITRIOL. Employ 50 c.c. of seminormal permanganate. The results are expressed as NO3H and NOaNa. The column y refers to acid of 140° Tw. as unit :— ■g ^1 NO3H. NOaNa. 11 NO3H. NOsNa. a. t. a. i. s a a. b. a. 6. y. g. per per g. per per y. g. per per g. per per CO. litie. cent. litre. cent. C.C. litre. cent. litre. cent. 10 78-75 4-61 106-29 6-22 36 21-88 1-28. 29-53 1-73 11 71-69 4-19 96-63 5-65 37 21-28 1-24 28-72 1-68 12 65-63 3-84 88-58 5-18 38 20-72 1-21 27-97 1-64 13 60-58 3-54 81-76 4-78 39 20-19 1-18 27-25 1-59 14 56-25 3-29 . 75-92 4-44 40 19-69 1-16 26-63 1-55 15 52-50 3-07 70-86 4-14" 41 19-21 1-12 25-83 1-51 16 49-22 2-88 66-43 3-88 42 18-75 1-10 26-31 1-48 17 46-32 2-71 62-52 3-65 43 18-27 1-07 24-66 1-44 18 43-75 2-56 59-05 3-45 44 17-90 1-05 24-16 1-41 19 41-45 2-42 55-95 3-27 45 17-76 1-02 23-67 1-38 20 39-38 2-30 53-15 3-11 46 17-12 1-00 23-11 1-35 21 37-50 2-19 50-61 2-96 47 16-72 0-978 22-57 1-32 22 35-80 2-09 48-32 2-83 48 16-41 0-960 22-15 1-30 23 34-24 2-00 46-21 2-70 49 16-04 0-938 21-65 1-27 24 32-81 1-92 44-28 2-59 50 15-75 0-921 21-26 1-24 25 31-50 1-84 42-52 2-49 65 14-32 0-837 19-33 1-13 26 30-29 1-77 40-88 2-39 60" 13-13 0-768 17-72 1-04 27 29-17 1-71 39-37 2-30 65 12-12 0-709 16-36 0-957 28 28-13 1-65 37-97 2-22 70 11-25 0-668 15-18 0-888 29 27-16 1-59 36-66 2-14 75 10-50 0-614 14-17 0-829 30 26-25 1-54 35-43 2-07 80 9-86 0-576 13-29 0-777 31 25-40 1-49 34-28 2-00 85 9-26 0-642 12-60 0-731 32 24-61 1-44 33-22 1-94 90 8-73 0-511 11-78 0-689 33 23-86 1-40 32-20 1-88 95 8-29 0-485 11-19 0-654 34 23-16 1-35 31-26 1-83 100 7-88 0-461 10-64 0-622 35 22-50 1-32 30-37 1-78 N.B. — The figures in colnmn a also indicate 0*01 lb. avoirdupois per gallon, or nearly ounces per cubic foot. the temperature not above 40° and by diluting the permanganate, say to 200 c.c. (The same method holds good for the analysis of sodium nitrite, but in this case the permanganate solution must be previously acidulated to such an extent that the NaNOj solution SULPHURIC ACID MANUFACTURE 137 is immediately decomposed when run into the permanganate.) Each cubic centimetre of the permanganate indicates 0'009502 g. N2O3, hence more or less of it is employed, according as to whether an acid containing more or less N2O3 is titrated. For chamber acid, employ at most 5 c.c. ; for good Gay-Lussac acid, up to 50 c.c. of permanganate. _ If the quantity of permanganate is called x, and that of the vitriol consumed for decolorising it y, the quantity of N2O3 present in grams per litre of acid is : — 9 -5 02a! Calculated as NO3H = as NaNOa = y The preceding table, p. 136, saves the calculation for all cases in which a; =50. The column y gives the number of cubic centi- metres of nitrous vitriol used, a the percentage in grams per litre, and b the percentage by weight, for acid of 140° Tw. (For other strengths the percentage by weight is calculated by dividing the figures of column a by 10 x specific gravity.) (b) Total Nitrogen Acids. — These are contained in sulphuric acid as N2O3, or more correctly as nitrososulphuric acid, 802(0 H)(ONO), and NO3H. NO can be present only in minute quantity, and only in absence of NO3H. N2O4 is decomposed by sulphuric acid into nitrososulphuric and nitric acid. The estimation made according to (a) only indicates N2O3. The total nitrogen acids are converted into NO by shaking up the nitrous vitriol with mercury ; the quantity of NO formed is estimated by volume (Crum's reaction). This is done by Lunge's Nitrometer, Fig. 9, p. 138. Fill the graduated limb a with mercury by raising the level tube & ; put the three-way tap so that it communicates with any of the openings ; run the nitrous vitriol into the top cup of a from a 1 c.c. pipette graduated in j^ c.c, employing only 0'5 c.c. of very strong, but up to 5 c.c. of very weak nitrous vitriol : lower the level tube, open the tap carefully so that the vitriol runs in without any air entering; pour 2 or 3 c.c. of pure strong sulphuric acid, free from nitrogen compounds, into the cup ; let this acid enter the nitrometer, and repeat the washing of the cup with 1 or 2 c.c. of pure acid. Start the evolution of gas by taking the tube a out of the clamp, inclining_ it several times till almost horizontal, and suddenly righting it again, so that mercury and acid are well mixed ; shake for one or two minutes till no more gas is evolved. Place the tubes so that the mercury in b is as much higher than that in a as is required for balancing 138 THE TECHNICAL CHEMISTS' HANDBOOK the acid in a ; this requires 1 mm. of Hg for 6 j mm. of acid. An exact reading can only be obtained when the gas has attained the temperature of the room and all froth has subsided. Read off the volume of the gas, also a thermometer hung up close by, and the barometer. In order to check the levelling, open the tap, when the level of a should not change. If it rises, the pressure has been in excess, and the reading must be increased a little, say by 01 c.c. If it sinks, the reverse is the case, i.e. always in the opposite sense to the change of level. Another plan is, to put a little acid into the cup before opening the tap. This wUl be sucked in if the pressure was too low, or raised if too high. With adroit manipulation the reading can then soon be corrected. Finally, lower the graduated tube a, lest any air should enter on opening the tap ; open the tap, raise the tube 6, force the gas and all acid into the cup, and turn the tap so that the acid flows through into a vessel held below ; the last portions are drawn off by blotting-paper. The nitrometer is then ready for the next experiment. A test must always be made to see whether the glass tap is gas-tight. It ivill hardly remain so without greasing it occasion- ally with vaseline, but this ought to be done very slightly, so as SULPHURIC ACID MANUFACTURE 139 to avoid any grease getting into the bore, for if the grease comes in contact with acid, troublesome froth is formed * 0.0. NO read off. a. Absolute weiglit, mg. 6. Per cent, by weight, wben em- ploying 1 CO. acid of 140° Tw. in the Nitrometer. Nitrogen, Nj .... Nitric oxide, NO . Nitrogen trioxide, N^Os Nitric acid, real, HNO3 Sodium nitrate, NaNOg Potassium nitrate, KNOg 0-6256 1-3403 1-6974 2-8143 3-7963 4-5176 0-0366 0-0784 0-0993 0-1646 0-2221 0-2642 (Multiples of these figures are given in Table 5, p. 15.) This process is interfered with by the presence of sulphurous acid, the best test for which is the smell. To remove it, tne acid is stirred up with a very small quantity of powdered potassium permanganate. Any great excess of this acid makes the process very troublesome and inaccurate. In highly concentrated acids a notable quantity (up to 3 per cent, by volume) of NO may be dissolved ; therefore a little water must be added to such acids in the nitrometer, sufficient to reduce their strength to about 90 per cent. H2SO4. The volume of NO read off is reduced to 0° C. and 760 mm. (32° F. and 29-92 in.) by means of the tables, pages 36 et seq., and calculated for the nitrogen compounds present by the table on this page, in which column a gives milligrams, b per. cent, by weight, when employing 1 C.C. acid of 140° Tw. Nitrometers (and gas-volumeters) should of course be obtained from a reliable dealer, so that the correctness of the graduations and the tightness of the taps can be depended upon. The reduction to 0° and 760 mm. can be effected without thermometer and barometer, and without the use of any tables, by means of Lunge's Gas-volumeter, Fig. 10, which serves also for numerous other analytical operations. It consists of the gas-measuring tube A, the reduction tube B, and the level tube C, all connected by thick rubber tubing with the three-way tube a. B and C are held in two arms of the same clamp, so as to be each either individually movable in its own arm, or both together by * Such froth may also be formed in the presence of too much water, by the separation of mercuric sulphate, but this hardly ever happens in the case of nitrous vitriol, and even in the analysis of sodium nitrate only when the description given for the estimation is not properly adhered to. 140 THE TECHNICAL CHEMISTS' HANDBOOK means of the common clamp. Tube A may be an ordinary nitrometer with three-way tap and funnel; it is, however, best employed merely as a gas-measuring tube, and for some pur- poses this tube is made to hold upwards of 100 c.c, in which case the upper portion is in the shape of a bulb, the division beginning below this, say, at 90 or 100 c.c. The most convenient shape, which serves both for small and large quantities of gas, is a tube possessing a bulb in the middle, and graduated above this from (at the tap) to 40 c.c, below the bulb from 100 to 140 c.c. A two-way tap, g, allows communication either with the straight outlet tube h, or with the right-angle tube e. Instead of carrying out the decomposition in tube A, it is decidedly preferable to employ for this purpose a separate tube, D, provided with a two-way tap, /, a funnel, d, and an outlet tube, c, corresponding to the tube e on A. D has its own level tube E. All these tubes are held in clamps, which can be moved up and down on the two bars of a heavy iron stand. The " reduction tube " B is enlarged at the top, and the narrow portion below is graduated from 100 to 125 c.c. in -^g C.C. It contains a volume of dry air which at 0° SULPHURIC ACID MANUFACTURE 141 and 760 mm. pressure would occupy exactly 100 c.c. This is obtained by taking, once for all, a reading of the thermom- eter and the barometer, and calculating what would be the volume of 100 c.c. of dry air under the prevailing atmospheric conditions. In reading the barometer, a deduction must be made for the expansion of the mercury, viz., 1 mm. between 0° and 12°, 2 mm. between 13° and 19°, 3 mm. between 20° and 25°. For calculating the volume of 100 c.c. air at " normal conditions " from the observed temperature * and the barometric reading 6 (corrected as above), we have the formula : — y _ 100(273 + 0760 2736 A drop of concentrated sulphuric acid is previously introduced through the open end of b, most conveniently by suction. After setting the level in B to the point indicated by the equation, the capillary end of b is sealed by fusing it up ; in order to prevent the heat from expanding the air in B, a cardboard shield is put between the flame and B. This is avoided by replacing the open capillary tube 6 by Lunge's "beaker-tap" (Ber., 1892, p. 3157), and still better by Gockel's gas-tap with annular mercury seal (supplied by Dr H. Gockel, Luisenstrasse 6, Berlin, N.W.)._ The "laboratory vessel" or "decomposition tube" D, in which the reaction is carried out, is provided with the fittings of an ordinary nitrometer, viz., the three-way tap /, the cup d, the lateral outlet c, and the special level tube E. It holds about 150 cc. and is not graduated. Mercury is poured in through E. By raising E, the vessel D is completely filled with mercury, till it begins to run out at c. The tap /is shut, the end of c closed by a glass or rubber cap, and the nitrous vitriol placed in d ; this is sucked into D, then some pure acid sucked in, to wash the cup and tap, tap / closed (no bubbles of air must remain below it !), and the decomposition brought about in the usual manner by shaking the vitriol with the mercury, to evolve all the nitrogen acids as NO. The tubes D and A are then brought opposite to each other (A having been previously filled, by raising 0, with mercury till it flows out at e) ; c and e are joined by a short piece of rubber tubing till they touch, so that no air remains in the space between ; C is lowered, E raised, and by cautiously opening tap /, the NO contained in D is transferred into A. As soon as all the gas is in A, and the acid following it has_ filled the narrow tube e, tap g is closed. Now tube C is raised tUl the mercury in B has risen to the mark 100, and B and C are simultaneously moved up or down, as may be required, till the levels in A and B coincide, that in B being still at 100 c.c. Since the air in B is now compressed to the point which it would occupy in the dry 142 THE TECHNICAL CHEMISTS' HANDBOOK state at 0° and 760 mm., and the gas in A is placed under exactly the same pressure (the temperature of these two parallel tubes being presumably the same), the reading in A gives the volume of NO reduced to the same conditions of 0° and 760 mm. The temperature in A and B must be exactly the same; this is ensured by the conductivity of the mercury, but in the case of large quantities bf NO it is necessary to wait at least ten minutes before finally adjusting the levels. If only one gas-volumeter is available, and that is adjusted for moist gases (as is required for other purposes), it may be used also for dry gases, but it is then necessary to avoid any sulphuric acid passing from D into A, and to suck a drop of water into A, before transferring the gas into it from D. Another way for measuring dry gases with a T/ioist reduction tube is as follows : observe the temperature ; take the tension of aqueous vapour corresponding to this from the table, p. 52=/, and adjust the mercury in the measuring tube A higher by/ mm. than in the reduction tube B, where, as usual, the mercury is adjusted by means of the level tube C to the point marking lOO'OO c.c. If, on the other hand, a reduction tube has been prepared for dry gases, by introducing a drop of concentrated acid, it may be used for Tnoist gases (as in the testing of manganese ore, bleaching powder, potassium permanganate, etc.), by adjusting the mercury in A/ mm. lower than in B. (c) Relative Proportions of the three Nitrogen Adds. — In order to find from the result of the permanganate titration and from the estimation of total nitrogen in the nitrometer (as NO) the relative proportions of N2O3, N2O4, and NO5H in a mixture of all three nitrogen acids absorbed by sulphuric acid, we may employ the following formula ; — a = c.c. NO found in the nitrometer. 5 = c.c. O, calculated from the permanganate titration. (1 c.c. = 1-4292 mg. ; 1 c.c. seminormal permanganate = 0-004 g. =2-7975 c.c. oxygen.) X = vols. NO, corresponding to the NgOj present. y=„ NO, „ „ N2O4 „ z = „ NO, „ „ NO3H „ If 46 be > a, x=ib-a; y = 2(a - 2b), or =a-x. If 46 be < u, y = ih i z = a- ib. (d) Qualitative Test for Traces of Nitrogen Acids. — These can be detected by means of diphenylamine. Dissolve a few grams of diphenylamine in 100 parts of pure sulphuric acid. This acid SULPHURIC ACID MANUFACTURE 143 should be completely free from nitrogen oxides, and can be made so, if not at hand, by boiling with a trace of ammonium sulphate. Dilate the acid with t'ffth volume of water before dissolving the diphenylamine. This solution may be employed at once, or kept, as it keeps quite well. Pour about 2 c.c. of the vitriol to be tested into a test-tube, and add about 1 c.c. of the diphenylamine solution so that the layers mix only gradually. In the case of dilute acids, or other lighter liquids, proceed in the opposite manner. The slightest traces of nitrogen acids are detected by the appear- ance of a brilliant blue colour at the area of contact of the liquids. The smallest traces of nitrous acid are detected, even in the presence of nitric acid, by the reagent proposed by Griess, as modified by Ilosvay and by Lunge. This reagent is prepared by (1) dissolvmg 0"5 g. sulphanilic acid in 150 c.c. dilute acetic acid'; (2) boiling O'l g. solid a-naphthylamine with 20 c.c. water, pouring the colourless liquid off from the purple residue, and mixing it with 150 c.c. dilute acetic acid. The two solutions are united, and can thus be kept for an indefinite time in a bottle, well pro- tected against air (which often contains traces of nitrogen acids). Add a few c.c. of this solution to the solution to be tested, and heat to 70° or 80°. If as little as 1 part nitrous acid be present in 1000 million parts of the liquid, a red colour is formed in about one minute. More concentrated solutions of HNO3, say 1 : 1000, do not yield the blue colour, but a yellow solution. In the presence of selenium the diphenylamine test fails, as Se gives the same reaction as nitrogen acids. In that case test for somewhat large quantities of nitrogen acids by the decoloration of indigo solution ; for traces, by the reddening of a solution of brucine sulphate. (e) Selenium in sulphuric acid can be recognised by adding to the acid a strong solution of ferrous sulphate, when a brownish- red precipitate will make its appearance, which cannot be con- fused with the colour produced by NO, or else by the green colour, produced in a solution of codein. (f) Exa/minationfor Lead. — Dilute the acid, if concentrated, with an equal volume of water and twice its volume of alcohol. Allow the mixture to stand for some time, filter any precipitate of PbS04, wash it with dilute alcohol, and dry and ignite in a porce- lain crucible, burning the filter separately. 1 g. PbSO4=0'6831 g. Pb. (g) Exammuxtionfor Iron. — Boil the acid, if free from nitrogen, with a drop of nitric acid to oxidise the iron. Dilute a little, allow to cool, and add a solution of potassium thiocyanate. A red colour proves the presence of iron. If there is not too little, it can be quantitatively estimated in another sample by heating with pure zinc (free from iron), pouring off from the zinc, washing 144 THE TECHNICAL CHEMISTS' HANDBOOK tte latter, allowing to cool, and titrating with, permanganate. This is best employed as ^th normal, indicating 0'002792 g. Fe per cubic centimetre. Not less than 50 c.c. of the acid should be taken for this test, as it generally contains very little iron. The smallest traces of iron can be estimated colorimetrically (Lunge, Zsch.f. angew. Chem., 1896, p. 3). (h) Arsenic is detected qualitatively by the well-known methods of Marsh or of Reinsch. For quantitative estimation dilute 20 c.c. of the acid with water, and treat with a current of SO2, until there is a strong smeU of the gas. This reduces As20g to AS2O3, but that requires a pretty long time and a considerable excess of SO2. Now drive off this excess by heating and passing in a current of CO2, neutralise exactly with Na2C03 and a little NaHCOs, and titrate with decinormal iodine and starch. 1 c.c. of the iodine solution indicates 0"004948 g. AS2O5. (Any consider- able proportion of iron should be previously removed.) (i) Chlorides. — Boil 10 c.c. of the acid in a flask, pass the vapours on to the surface of a little water, contained in a flask, and estimate the absorbed HCl acidimetrically, or after neutral- ising with NajCOa, by titrating with decinormal sUver nitrate (p. 146). 11. Analysis of Fuming Sulphuric Acid (Nordhausen Oil of Vitriol) and of Sulphuric Anhydride. The substance is either weighed in glass bulbs or in a glass- tap tube. The former are very thin bulbs of about 2 cm. diameter, ending on each side in a capillary tube. Melt the acid, if solid, till it is completely homogeneous, and suck 3 g. to 5 g. into the bulb, which ought to be half-filled with it. The sucking is best done by means of a bottle closed with a rubber cork, through which passes a tightly fitting glass tap, connected at its free end with a rubber tube. Suction is applied to the latter, the tap closed, the rubber tube drawn over one of the capillary ends of the weighing bulb, and by opening the tap a sufficient quantity of acid admitted into the bulb. The tube is cleaned outside, and one of the capillary ends is sealed off. The other end can be left open without fear of any loss of SO3 or attraction of moisture during weighing. The weighing is best done FiQ. 11. on a small platinum crucible with two nicks, on which the ends of the bulb can rest. If the latter should be accidentally broken, the acid runs into the crucible, not on to the balance. Put the bulb, after weighing, open SALTCAKE AND HYDROCHLORIC ACID 145 end downwards into a small Erienmeyer flasb, into the neck of which it ought to fit exactly (Fig. 11), and which contains so much water that the capillary tube dips well into it, to prevent any loss of SO3 on mixing the acid with water. Break oflf the other point, allow the acid to run out, squirt a few drops of water into the upper capillary, and ultimately rinse the whole bulb tube by repeated aspiration of water. Dilute the liquid to 500 c.c. and take 50 c.c. for each test. This is done with i normal sodium carbonate solution (1 c.c.=O'OO8O07 g. SO3), and methyl orange as indicator. From the acidity found, that due to SO2 is_ deducted, which is ascertained by titrating another sample with iodine. Lunge and Key's glass-tap pipette (Fig. 12) r-ag (the taps of which must be tight without greas- ing !) is more convenient than the bulb tube. Shut the lower tap c, open the upper tap a, apply suction (with the mouth) at d, and shut a whilst sucking. Immerse the point e in the acid to be tested, and open c ; the partial vacuum in bulb b suffices for drawing up enough acid, which must not be allowed to reach the tap c. Shut c, clean the point e, put the pipette in the outer glass vessel/, and weigh. Take the pipette out of /, place it point downwards in water, and slowly run out the contents. Then squirt some water from above into 6, allow to stand for a moment, and rinse thoroughly with water. The strongest fuming oil of vitriol cannot be run directly into water without loss. Such oil of vitriol is weighed out in small glass bulbs, as described above; both ends are sealed up, the bulb is placed in a bottle con- taining a considerable quantity of water, the stopper put in, the bulb broken by shaking the bottle, and after waiting a little the solu- tion titrated. Solid products of this class must be melted F""- i^- by moderate heating ; they then remain long enough in the liquid state to complete the weighing and run- ning out without being heated again. But products which are not far removed from real SO3 in composition would give out too much vapour in this operation. Such products are weighed out in a stoppe'red bottle, and mixed in this with a known and exactly analysed quantity of monohydrate, at a temperature of 30° to 40° C. This ought to produce a mixture containing about 70 per eent. SO3 which will remain liquid at ordinary temperatures. K 146 THE TECHNICAL CHEMISTS' HANDBOOK If only 0'5 to 1 g. of acid has been weighed off, titrate directly. This is more accurate than diluting and titrating only part of the liquid, but the latter method cannot be avoided when a larger quantity of acid has been weighed. The acidinietric determination, of course, indicates the total percentage of acid. From this we must deduct in the first instance any SO2 present. This is estimated in the usual way by deci- normal iodine, and for each c.c. of this 0'05 c.c. normal sodium carbonate solution is deducted (since with methyl orange the colour changes when SO2 has passed into NaHSOa). If we call the c.c. of normal sodium carbonate used =to, those of decinormal iodine used for the same quantity of oil of vitriol =7re, the acidity due to H-2SO4+SO3 is=(n-0-05 m) 0-040035 SO3. To the SO3 thus found add the SO2 (calculated =0'0032035 m), and assume the residue to be water.* By multiplying this HjO by 4'445, we obtain the quantity of SO3 combined with it to form H2SO4, and by deducting this from the total SO3 acidity, that of the free SO^. in. SALTOAKB AND HYDROCHLORIC ACID. A. — Salt (Common Salt, Rock-Salt). 1. Moisture. — Ignite 5 g. of salt in a covered platinum crucible (to prevent loss by spirting) ; heat first quite gradually, then for some minutes, up to a low red heat. If the sample is too damp, or if several samples are to be tested at the same time, weigh off the 5 g. samples in fiat-bottomed Erlenmeyer flasks, with funnels on, heat a number of these on a sand-bath for three or four hours to 140° or 150° (without funnel), and allow them to cool with the funnel in, which saves the use of a desiccator. Afterwards the small remainder of chemically combined water may be removed by heating on a wire-gauze, but this is mostly unnecessary. 2. Insoluble matter. — Dissolve 5 g., filter the insoluble matter, wash, dry, and ignite. 3. Chlorine. — Weigh off 5"846 g. of the moist salt, dissolve it, and dilute to 500 c.c. ; take out 25 c.c. by means of a pipette, add so much of a solution of neutral potassium chromate that the liquid is distinctly _ yellow, and titrate vsdth decinormal silver solution (cf. Appendix). Add the silver solution from a 50 c.c. • In case any weighaMe quantity of solid impurities is present, this must be of course equally deducted. SALTCAKE AND HYDROCHLORIC ACID 147 burette, till the precipitate, even after agitation, shows a distinct but_ faint pink colour. 0"2 c.c. is deducted from the number of cubic centimetres of silver solution used, as being required for producing the colour. The remainder, multiplied by 2, gives the percentage of NaCl in the salt. In lieu of potassium chromate, sodium arsenate may be employed as indicator. This is even more sensitive, and no deduction from the silver solution used should be made in this case. 4. Lime. — Dissolve 5 g. of the salt in water, if necessary with the aid of a little HCl. When analysing impure roct-salt, the treatment with dilute HCl must be continued for some time, in order to dissolve all CaS04. It is also necessary to filter' off any clay, etc., but non-argillaceous salt ought to dissolve com- pletely, excepting any grains of sand and the like. In the clear solution precipitate the lime with ammonia and ammonium oxalate, allow to stand for twelve hours, filter the precipitate through a fine filter-paper in a well-shaped funnel (c/. p. 109), wash, dry, and ignite it in a platinum crucible till it is completely converted into CaO. This is done by first gently heating till the calcium oxalate is decomposed, and then igniting at nearly a white heat for twenty minutes, either over a gas blowpipe or, more conveniently, in a Hempel's gas-oven or over a Muencke . burner. One part CaO is equal to 2-4281 CaSOi, and is calcu- lated as such. 5. Sulphates. — Dissolve 10 g_. of the salt in tepid water, with addition of a little hydrochloric acid. Dilute to 1 litre, filter through a dry pleated filter, and precipitate 250 c.c. (=2"5 g. salt) by barium chloride {cf. p. 108). The sulphate is usually calculated as CaS04. 6. Magnesium chloride may be titrated directly by drying the salt, extracting it with absolute alcohol, filtering, evaporating off the alcohol from the filtrate (which contains nothing but MgClj), and titrating with silver nitrate. B. — Saltcake (Sulphate of Soda). (N.B. — Nos. 1 and 2 are suflScient for the daily checking of the manufacture -, the others are employed for saltcake when bought and sold.) 1. Free Add. — Dissolve 20 g. saltcake, dilute to 250 c.c, take out 50 c.c. with a pipette, and methyl orange, and titrate with standard sodium carbonate to the point of neutralisation. Each 148 THE TECHNICAL CHEMISTS' HANDBOOK cubic centimetre of the standard alkali is equal to 1 per cent. SO3. The total acidity is calculated as SO3, including HCl and NaHS04. (If litmus were employed as indicator, the presence of salts of ■ iron and alumina would cause trouble in the titration ; with methyl orange this is nat the case.) 2. Sodium GUoride. — Take another 50 c.c. of the solution made for the test No. 1, add the same quantity of standard alkali as used for this test, so that the acid is exactly neutralised, then a little neutral potassium chromate, and titrate with decinormal silver solution, as in A, 3. Each cubic centimetre of silver solution (after deducting 0'2 from the whole) is equal to 0'1462 per cent. NaCl. Or else employ a solution containing 2*906 g. AglSfOs per litre and indicating 0"001 g. NaCl per cubic centimetre. This would, in the present case, indicate 0'025 per cent. NaCl per cubic centimetre. 3. Iron. — Dissolve 10 g. of sulphate in water, reduce the iron salts to the ferrous state by a little sulphuric acid and zinc, and titrate with potassium permanganate {cf. p. 143). 4. Residue, insoluble in water, is estimated as usual, if present. 5. Lime. — Dissolve 10 g, in water, if necessary with a little HCl ; add NH4CI and NH3, precipitate with ammonium oxalate, ignite, and weigh as CaO {cf. A, 4). If any appreciable quantity of FegOs has been found, this must be deducted. 6. Magnesia is precipitated in the filtrate from No. 5 by ammonium phosphate ; allow to stand for twenty-four hours ; filter, wash with dilute ammonia, dry, ignite, and weigh the magnesium pyrophosphate, of which 1 part=0'3621 MgO. 7. Alumina. — The solution of the saltcake is precipitated by ammonia (free from CO2). The precipitate is ignited and weighed. Deducting the weight of FcjOj found in No. 3, the remainder is=Al203. 8. Sodium Sulphate {direct estimation). — Dissolve 1 g. of the saltcake ; precipitate any lime together with ferric oxide, etc., as in No. 5 ; filter ; evaporate the filtrate to dryness after adding a few drops of pure sulphuric acid ; ignite ; repeat this after adding a small piece of ammonium carbonate, and weigh. Deduct from this weight (1) the NaCl found in test No. 2, calculated for Na2S04 (1"0000 NaCl = 1 "2151 NagSOi, or each cubic centimetre of decinormal silver solution employed in test No. 2=0'001776 g. Na2S04) ; (2) the MgO found in test No. 6 calculated as MgSOj (1-000 MgO=2-9859 MgS04). The remainder is equal to the sodium sulphate actually present in 1 g. saltcake. SALTCAKE AND HYDROCHLORIC ACID 149 C. — Chimney-Testing, Act of Parliament. — By the Alkali Works Eegulation Act of 1906, it is enacted that " Every alkali work shall be carried on in such a manner as to secure the condensation to the satisfaction of the chief inspector, (as) of the muriatic acid gas evolved in such ■work to the extent of 95 per centum, and to such an extent that in each cubic foot of air, smoke, or chimney gases escaping from the works into the atmosphere, there is not contained more than one-Jifih 'part of the grain [=0'457 g. per cubic centimetre] of muriatic acid ; (6) of the acid gases of sulphur and nitrogen which are evolved in the process of the manufacture of sul- phuric acid in that work to such an extent that the total acidity of such gases in each cubic foot of residual gases after com- pletion of the process, and before admixture with air, smoke, or other gases, does not exceed what is equivalent to four grains of sulphuric anhydride ; (c) in the residual gases from the con- centration of distillation of sulphuric acid, the total acidity of gases in each cubic foot must not exceed the equivalent of Ij grain of sulphuric anhydride." Hyd/rochloric Acid in Chimney Gases. — In order to ascertain the HCl in chimney gases, an aspirator is used known as Fletcher's flexible aspirator, or bellows. This aspirator is supposed to draw at one aspiration one-tenth of a cubic foot. It is not safe to trust to this supposed capacity, and moreover the capacity of a new aspirator varies for some time. To ascertain the real capacity, fill a very large beaker or other cylindrical vessel with water, and invert it under water. Completely fill the aspirator with air, and expel this air into the inverted beaker. Mark the point to which the beaker is filled when the water inside the beaker is level with that outside. Measure the capacity of the beaker to that mark; say it contains V cubic centimetres of water. Then the number of aspirations which must be made with this aspirator in order to draw 1 cubic foot of air is : — j^ ^ 28290. or if the capacity of the beaker is measured in grains ; — jj ^ 436485 N will usually be a mixed number, but the nearest integral number is substituted, and it will be safest to substitute the next higher integral number. Thus, if N be found 9"3, it will be safest 150 THE TECHNICAL CHEMISTS' HANDBOOK to consider 10 as the number of aspirations necessary to draw 1 cubic foot. The aspirator must be air-tigbt. The gas is with- drawn from the chimney through a glass tube, which should be sufficiently long to reach a considerable distance into the chimney, say 6 feet. The glass tube should be of at least | in. diameter, otherwise the aspiration is tedious. In flues where the tempera- ture is too high for glass, a platinum tube must be employed. The bellows and tube are washed with distilled water until the washings give no reaction with silver nitrate. 100 or 200 cubic centimetres of distilled water, free from chloride, are then charged into the bellows, and after each aspiration the gas is well washed by shaking the contents of the aspirator violently. When the number N of aspirations has been made, some water is forced into the glass tube, and allowed to flow back into the bellows to wash out any acid which may have condensed in the tube. The liquid is then transferred into a porcelain dish (or into a beaker standing on a porcelain slab). If the liquid is so highly charged with soot that it would be impossible to recognise the change of colour, it miist be filtered through a filter previously washed free from chlorides. The liquid is then oxidised by potassium permanganate, and any excess of this reagent removed by a trace of ferrous sulphate, neutralised by pure sodium carbonate, coloured by potassium chromate, and titrated with decinormal silver solution. (See p. 146 A, 3, and Appendix.) Some use a oentinormal silver solution. Call the number of cubic centimetres consumed =a;; then the hydrochloric acid, in grains per cubic foot of gas, will be ; — G = 0-05633a; grains. In order to calculate the percentage escape, the velocity of the gas in the chimney must be ascertained and reduced to 60° F. No notice is usually taken of the barometric pressure, since the measurement by the bellows is anyhow inaccurate. In addition, the diameter of the chimney and the number of tons of salt decomposed during twenty-four hours in the furnaces connected with the chimney must be known. If G = number of grains of HCl per cubic foot. If V = velocity at 60° F. in feet per second, If D = diameter of chimney at testing-hole in feet. If T = tons of salt decomposed per twenty-four hours assumed to contain 93 per cent. NaCl, the percentage escape will be : — 0-7468 X GW_ SALTCAKE AND HYDROCHLORIC ACID 151 D. — Testing of the Gases in the Hargreaves' Process. (a) Total acidity, as described p. IIV. (b) Svlphur dioxide, as p. 116. (c) Hydrogen chloride is estimated in the sample taken for (a), as described p. 149. By deducting (b) and (c) from (a), the amount of SO3 is found. LE.— Hydeochloeic Acid 152 THE TECHNICAL CHEMISTS' HANDBOOK E. — Hydrochloric Acid. SPBCIFIO GRAVITY OF PURE HYDROCHLORIC ACID AT 15° C. COMPARED 'WITH -WATER AT 4°, AND REDUCED TO VACUUM. (Iiunge and Marchlewskl. ) 100 parts by weight correspond to Specific parts by weight of (&avity llitre 1 cubic Degrees contains foot Twaddell. Acid of Acid of g. of contains 4 in vacuo. HCl. spec, gravity 1-1426 = 28-6°Tw. spec, gravity 1-162 = 30-4° Tw. Hca. lbs. ofHCI. 1-000 0-16 0-57 0-53 1-6 0-10 1 1-006 1-15 4-08 3-84 12 0-75 2 1-010 2-14 7-60 7-14 22 1-37 3 1-015 3-12 11-80 10-41 32 1-99 4 1-020 4-13 14-67 13-7? 41 2-62 6 1-025 5-16 ns-so' 17-19 ~ 3-30 6 1-030 6-16 21-86 20-53 64 3-99 7 1-035 7-15 26-40 23-87 74 4-61 8 1-040 8-16 28-99 27-24 85 6-30 9 1-045 9-16 32-55 30-58 96 5-98 10 1-050 10-17 36-14 33-95 107 6-67 11 1-065 11-18 39-73 37-33 118 7-35 12 1-060 12-19 43-32 40-70 129 8-04 13 1-065 13-19 46-87 44-04 141 8-79 14 1-070 14-17 50-35 47-31 152 9-48 15 1-075 16-16 63-87 60-62 163 10-16 16 1-080 16-15 67-39 63-92 174 10-85 17 1-086 17-13 60-87 57-19 186 11-69 18 1-090 18-11 64-35 60-47 197 12-28 19 1-096 19-06 67-78 63-64 209 13-03 20 1-100 20-01 71-11 66-81 220 13-71 21 1-105 20-97 74-52 70-01 232 14-46 22 1-110 21-92 77-89 73-19 243 15-16 23 1-115 22-86- 81-23 76-32 255 15-90 24 1-120 23-82 84-64 79-63 267 16-66 2S 1-125 24-78 88-06 82-74 278 17-33 26 1-130 26-75 01-60 86-97 291 18-14 27 1-135 26-70 94-88 89-16 303 18-89 28 1-140 27-66 98-29 92-35 315 19-64 29 1-145 28-61 101-67 96-52 328 20-45 30 1-160 29-57 • 106-08 98-73 340 21-20 31 1-155 30-65 108-68 102-00 363 22-01 32 1-160 31-62 112-01 106-24 366 22 82 83 1-165 32-49 115-46 108-48 379 23-63 S4 1-170 33-46 118-91 111-71 392 24-44 35 1-176 84-42 122-32 114-92 404 25-19 36 1-180 35-39 125-76 118-16 418 26-06 37 1-186 36-31 129-03 121-23 430 26-81 38 1-190 37-23 132-30 124-30 443 27-62 3!l 1-196 38-16 186-61 127-41 456 28-43 , 40 1-200 . 39-11 138-98 130-58 469 29-24 SALTCAKE AND HYDROCHLORIC ACID 153 INFLUENCE! OF TEMPERATURE! ON THE SPECIFIC GRAVITY OF HYDROCHLORIC ACID. 0°. 5'. 10'. 16'. 20°. 25°. 30°. 35°. 40°. 45°. 50° 1-168 1-158 1-148 1-138 1-128 1-118 1-108 1-098 1-088 1-078 1-068 1-058 1-048 1-038 1-028 1-018 1-165 1-155 1-145 1-135 1-125 1-115 1-105 1-095 1-085 1-075 1-065 1-065 1-045 1-035 1-026 1-016 1-163 1-163 1-143 1-138 1-123 1-113 1-103 1-093 1-083 1-073 1-063 1-063 1-043 1-033 1-023 1-013 1-160 1-150 1-140 1-130 1-120 1-110 1-100 1-090 1-080 1-070 1-060 1-050 1-040 1-030 1-020 1-010 1-157 - 1-147 1-137 1-127 1-117 1-107 1-097 1-087 1-077 1-068 1-058 1-048 1-037 1-027 1-017 1-007 1-154 1-145 1-134 1-125 1-115 1'105 1-095 1-085 1-075 1-065 1-055 1-045 1-036 1-024 1-014 1-004 1-152 1-142 1-132 1-122 1-112 1-103 1-092 1-082 1-073 1-063 1-063 1-043 1-032 1-022 1-012 1-002 1-U9 1-139 1-J29 1-119 1-110 1-101 1-090 1-080 1-070 1-061 1-050 1-040 1-030 1-019 1-009 0-999 1-147 1-137 1-127 1-117 1-108 1-099 1-088 1-077 1-008 1-059 1-048 1-038 1-027 1-017 1-007 0-997 1-144 1-134 1-125 1-114 1-106 1-097 1-086 1-075 1-066 1-057 1-046 1-036 1-025 1-014 1-004 0-994 1-142 1-132 1-123 1-112 1-103 1-094 1-084 1-078 1-064 1-055 1-044 1-033 1-022 1-012 1-002 0-992 56'. 60°. 65'. 70°. 75\ 60°. 85°. 90°. 95°. 100°. 1-140 1-130 1-120 1-109 1-101 1-093 1-082 1-on 1-062 1-053 1-042 1-031 1-020 1-010 1-000 0-990 1-138 1-128 1-118 1-107 1-099 1-090 1-080 1-069 1-060 1-051 1-040 1-029 1-018 1-008 0-998 0-988 1-136 1-126 1-116 1-104 1-096 1-088 1-078 1-067 1-058 1-049 1-038 1-027 1-016 1-005 0-995 0-985 1-133 1-123 1-113 1-102 1-094 1085 1-076 1-065 1-056 1-048 1-036 1-025 1-014 1-003 0-003 0-983 1-131 1-121 1-111 1-100 1-091 1-083 1-073 1-063 1-064 1-046 1-034 1-023 1-011 1-001 0-991 0-981 1-129 1-119 1-108 1-097 1-089 1-080 1-071 1-061 1-053 1-044 1-033 1-021 1-009 0-990 0-980 0-979 1-127 1-116 1-106 1-096 1-086 1-078 1-069 1-059 1-051 1-043 1-031 1-019 1-007 0-997 0-987 0-977 1-125 1-114 1-104 1-093 1-084 1-075 1-066 1-067 1-049 1-041 1-029 1-017 1-005 0-995 0-985 0-975 1-123 1-112 1-102 1-090 1-081 1-073 1-064 1-055 1-047 1-039 1-027 1-015 1-003 0-993 0-983 0-973 1-121 1-110 1-009 1-088 1-079 1-070 1-001 1-053 1-045 1-037 1-025 1-013 1-001 0-991 0-981 0-971 3. ANALYSIS OF HYDROCHLORIC ACID. (a) Estimation of HCl. — Measure ofif, by means of an accurate pipette, 10 c.c. of the acid, the specific gravity of which should be known, dilute to 200 c.c, take out 10 c.c. Or else employ a glass- tap pipette, as described p. 145, for fuming sulphuric acid ; in this case its contents are run into water and employed directly for 154 THE TECHNICAL CHEMISTS' HANDBOOK titration. Add sodium carbonate, free from chloride, till the reaction is neutral or faintly alkaline. This point will be hit quickly, and without the loss of many drops for testing, if the percentage of the acid is ascertained from its specific gravity by the table (p. 152) and the corresponding quantity of sodium carbonate solution is run in from a burette. Now add a little neutral potassium chromate, and titrate with decinormal silver solution till a faint pink colour is produced (c/. p. 146). Deduct 02 c.c. from the silver solution employed ; the remainder, multiplied by 72'94 and divided by the specific gravity of the acid, indicates its percentage of HCl." This test would fail in the presence of metallic chlorides, which are, however, hardly ever present in appreciable quantity in ordinary hydrochloric acid. The free HCl can also be ascertained by estimating the total acidity and deducting therefrom that due to sulphuric acid, making allowance for any sodium sulphate present. (b) Estimation of Svlj^huric Acid. — Neutralise the acid almost, but not quite, with sodium carbonate free from sulphate, and precipitate the sulphuric acid by barium chloride, as on p. 108. If the acid be partially saturated with NH3, or not saturated at all, the result is too low. Each part of BaS04 is equal to 0"3430SO3. (c) Estimation of Iron. — Reduce this to ferrous iron by d igesting the acid for a short time with a rod of zinc free from iron, wash the rod, dilute the whole with water, add some manganous chloride or sulphate (in order to counteract the action of HCl on permanganate), and titrate with a twentieth normal solution of potassium permanganate, each cubic centimetre of which indicates 0'002792 g. Fe. In case of SO2 being present, this must first be oxidised to sulphuric acid, before reducing the ferric salt and titrating. (d) Free Chlorine. — Introduce a sample of the acid into a flask, remove the air from the empty space by CO2 ; shake the acid with a strip of clean metallic copper. The latter is converted into chloride by the free chlorine, and the copper thus dissolved can be detected by potassium ferrocyanide, etc. This will show the smallest traces of chlorine. For ordinary purposes it is sufllcient to heat the acid gently and hold a strip of KI starch paper in the vapour ; this will at once turn blue in the presence of free CI. (e) Svlphur dioxide.— O^iAxs^ with permanganate, or iodine, or H2O2 to sulphuric acid, estimate the total H2SO4 now present as in No. 2, and deduct the quantity there found ; the remainder = S02. (f) Arsenic. — Eeduce all to trichloride by passing in SO2 for some time, and precipitate by H2S as AS2S3. Wash the precipitate, dissolve it on the filter in ammonia, evaporate the solution in a glass or porcelain dish, dry at 100°, and weigh. One part AS2S3 =0-6091 As =0-8041 AS2O3. BLEACHING POWDER, ETC. 155 IV. BLEACHING POWDER AND CHLORATE OP POTASH MANUFACTURE. A. — Natural Manganese Ore. 1. Mcmganese Dioxide. — Weigh r0866 g. of manganese ore, ground as fine as possible, and dried for some time at 100° C. ; put it into the flask (Fig. -13) closed by a rubber (Bunsen) valve, or, preferably, into a flask provided with a Contat-Gockel bulb (Fig. 14), which has been half-filled with a concentrated solution of sodium carbonate ; put into the flask 75 c.c. (in three portions with a 25 c.c. pipette) of a solution containing Fig. 14. 100 g. pure crystallised ferrous sulphate and 100 c.c. pure con- centrated sulphuric acid, diluted to 1 litre, and standardised on the same day by means of the same 25 c.c. pipette, with deci- normal potassium permanganate. Close the flask with its cork or valve, and heat till the manganese is completely decomposed, leaving a light-coloured residue. On cooling, the valve must act properly, which will be seen by the collapsing of the rubber tube, Fig. 13, or by the running in of sodium carbonate solution, Fig. 14. After complete cooling add 200 c.c. of water, and titrate with potassium permanganate to a faint pink coloration. Deduct the quantity of permanganate required from that correspond- ing to the 75 c.c. of iron solution ; the remainder indicates for each cubic centimetre 0'02173 g., equal to 2 per cent. Mn02. 2. Carbon Dioxide is estimated gravimetrically by expelling it with dilute sulphuric or nitric acid and absorbing it with soda-lime, by means of the apparatus and process described (p. Ill, No. 6). Or more quickly by Lunge and Rittener's gas-volumetric process, see p. 171. 156 THE TECHNICAL CHEMISTS' HANDBOOK 3. Estimation of the Hydrochloric Acid required for Decom- posing the Ore. — Dissolve 1 g. of manganese ore in a flask provided with a reflux condenser in 10 c.c. of ordinary strong hydrochloric acid the titre of which is known, employing heat as far as necessary. Allow the solution to cool, and add standard alkali till reddish- brown flakes of ferric hydroxide appear, which do not redissolve on agitation. Calculate the standard alkali corresponding to the acid employed for dissolving the ore, and deduct the quantity thus found from the 10 c.c. flrst employed. B. — Recovered Manganese Mud and Weldon Liquors. 1. Mn02 in Weldon Mud. — Standardise an acid iron solution (100 g. pure crystallised ferrous sulphate +100 c.c. pure concen- trated sulphuric acid in 1 litre) by seminormal potassium permanganate {cf. Appendix), by diluting 25 c.c. of the former with 100 c.c. or 200 c.c. of cold water, and adding the permanganate from a stopcock burette, till, on agitating, the pink colour is not discharged immediately, but remains at least for half a minute. Subsequent decolorisation is not taken into account. This test should be made once each day. Call the cubic centimetres of permanganate employed x. Now, put another 25 c.c. of the iron solution into a beaker. Take 10 c.c. of manganese mud out of the well-shaken bottle (mere stirring does not ensure a proper mixture) containing it ; wash the pipette outside, run its contents into the beaker containing the iron solution, and wash the mud remaining inside into the same beaker. When all has dissolved, on agitating, add 100 c.c. of water, and titrate by potassium permanganate. The number of cubic centimetres now used we call y. The quantity of Mn02 in grams per litre of mud equals 2'i73 (x-y). 2. Total Manganese of the Mud, expressed in Grams of theoretically possible Mn02 per Litre. — Take 10 c.c. of the mud, with the same precautions as in test No. 1. Boil with strong hydrochloric acid till all chlorine is driven ofi'; saturate the excess of acid by ground marble or precipitated calcium carbonate ; add a concentrated filtered- solution of bleaching powder ; boil a few minutes till the colour turns a decided pink, and the excess of bleaching powder can be smelt, and again destroy the pink colour by adding alcohol drop by drop. All manganese is now present as Mn02 ; filter and wash. The filtrate should not produce any brown colour with a bleaching-powder solution, which would show the presence of Mn in solution. Continue the washing till starch and KI do not give any reaction. Transfer the filter with the precipitate into 25 c.c. of the acid iron solution employed in test No. 1. If all Mn02 is not dissolved, add another 25 c.c. of BLEACHING POWDER, ETC. 157 iron solution; dilute witli 100 c.c. of water, and titrate with permanganate. Calculation as in No. 1. 3. Estimation of the " Base," i.e. the Monoxides, etc., of the Mud which combiTie with HCl without yielding Free Chlorine. — Dilute 25 CO., or in case of a very rich base 50 c.c, of normal oxalic acid (63"03 g. crystallised oxalic acid in 1 litre) to 100 c.c. ; heat to 60° to 80° C., add 10 c.c. manganese mud by means of a pipette, with the precautions stated in No. 1, and agitate till the colour of the precipitate is no longer yellowish but pure white, which ought to take place very soon at the above temperature. Dilute to 202 c.c. (2 c.c. correspond to the volume of the precipitate, and are marked on the neck of the 200 c.c. flask) ; pour through a dry filter, and titrate 100 c.c. of the filtrate with standard alkali, employing phenolphthalein as indicator. (Methyl orange is not applicable for oxalic acid.) Call the number of cubic centimetres of standard alkali used, z. The oxalic acid serves (1) for reducing the Mn02 with formation of MnO and COj ; (2) for saturating the MnO thus formed ; (3) for saturating the monoxides originally present, i.e. the base. The oxalic acid not thus used is equal to 22!. The acid used for reducing MnOj is equal to that used for neutralising the MnO formed, and both amounts together are equal to the value x — y obtained by the Mn02 test, since the oxalic acid is normal and the permanganate half normal. The amount of oxalic acid consumed by the bases of the mud is found by deducting from the total acid used that required for the Mn02 {x - y), and that which was not neutralised at all by the mud = 2z, therefore in all a; - y - 2z. The " base " is equal to the ratio of this value to that found in test No. 1, viz., „' • It is, therefore, if 25 c.c. of oxalic acid had been employed, equal to: 50-2a!-4z + 2y _ / 50-4z \ _ g. x-y \ x-y ) or, if 50 cc had been employed, equal to : — 2. / 100-fe \ C. — Limestone. 1. Insoluble Matter. — Dissolve 1 g. in hydrochloric acid, filter the residue, wash, dry, and ignite. In the presence of appreci- able quantities of organic matter, weigh the filter after drying at 100°, and ignite afterwards. The difference is calculated as organic matter. 2. Lime. — Dissolve 1 g. in 25 c.c. normal hydrochloric acid 158 THE TECHNICAL CHEMISTS* HANDBOOK and titrate with normal alkali. Deduct the volume of the latter used from 25 and multiply the remainder with 2'8 to find the percentage of CaO, or with 5 to find that of CaCOs. (iT.^.— Here MgO is calculated as CaO. This is admissible for most limestones employed in alkali and bleaching-powder making, because they contain but little MgO ; otherwise the MgO or MgCOs found as in No. 3 must be deducted.) 3. Magnesia need only be estimated in limestone used for manganese recovery. Dissolve 2 g. of limestone in HCl, precipi- tate the CaO by NH3 and ammonium oxalate, and precipitate the magnesia in the filtrate by sodium phosphate (c/. p. 148). 4. Iron is usually estimated only in limestone used for bleach- fng-powder making. Dissolve 2 g. HCl, reduce by zinc, dilute, add some manganese solution free from iron, and titrate by permanganate (c/. p. 143). D. — Quicklime. 1. Free CaO.— Weigh 100 g. of an average sample carefully taken, slake it completely, put the milk into a half -litre flask, fill up to the mark, shake well, take 100 c.c. out, run it into a half- litre flask, fill up, mix well, and employ 25 c.c. of the contents, equal to 1 g. quicklime, for the test. Titrate by normal oxalic acid and phenolphthalein as indicator, adding the a,cid very slowly and shaking well after each addition. The colour is changed when all free lime has been saturated and before the CaCOs is attacked. One c.c. normal HCl =0-02804 g. CaO. 2. Carbon Dioxide.— TitT&te CaO and CaCOj together by dissolving in an excess of standard hydrochloric acid and titrating back with standard alkali. By deducting the CaO estimated as in No. 1 the quantity of CaCOs is obtained. For very accurate estimations the CO2 is expelled by HOI, absorbed in soda-lime, and weighed ; or it is estimated by volume in Lunge and Eittener'a apparatus (p. 171). S. — Slaked Lime. 1. Water. — Weigh about 1 g. in a stoppered glass tube, and heat it gradually in a platinum crucible, at last to a strong red heat (c/. p. 146) ; allow to cool in the exsiccator, and weigh. The loss of weight is equal to HjO + CO2. 2. Carbon Dioxide is estimated as above in D, 2. 3. Estimation of the percentage of Caustic Lime in Milk of Lime by means of the specific gravity (Blattner). — Thin miUc of lime is poured into the cylinder and the reading of the hydrometer is taken quickly, before the lime subsides. For thick milk of lime employ a somewhat wide cylinder, put the hydrometer in without BLEACHING POWDER, ETC. 159 using any force and turn the cylinder slowly round, so that it receives a slight shaking, until the hydrometer ceases to sink. The following table is valid for 15° C. TABLE SHOWING AMOUNT OP LIMB IN MILK OF LIMB. (Calculated from Blattner.) Degrees Grms. CaO Lbs. CaO per Degrees Grms. OaO Lbs. CaO per Twaddell. per litre. cubic foot. Twaddell. per litre. cubic foot. 2 11-7 0-7 28 177 11-1 4 24-4 1-5 30 190 11-9 6 37-1 2-3 32 203 12-7 8 49-8 3-1 34 216 13-5 10 62-5 3-9 36 229 14-3 12 75-2 4-7 38 242 15-1 14 87-9 5-5 40 265 15-9 16 100 6-3 42 268 16-7 18 113 7-1 44 281 17-6 20 126 7-9 46 294 18-4 22 138 8-7 48 307 19-2 24 152 9-5 50 321 20-0 26 164 10-3 P. — Bleaching Powder. 1. Available GMorine (Penot's Method)— Weigh. 7;092 g. of the sample, previously well mixed ; grind it with a little water in a porcelain mortar (the lip of which has been greased a little underneath) till a completely homogeneous thin paste has been obtained ; dilute with more water, wash the whole into a litre flask, fill up_ to the mark, and take for each test 50 c.c.=0'3546 g. bleaching powder, having shaken up the flask immediately before. Run into the above, with continuous agitation, an alkaline decinormal arsenite solution, containing 4"948 g. AS2O3 per litre (cf. Appendix) till the expected point is not very far off. Then place a drop of the mixture on to a piece of filter paper, moistened with a starch solution con- taining potassium iodide. If there is very much chlorine left, a brown spot will be produced ; if less chlorine, the spot will be blue. According to the depth of this colour more or less arsenite solution is run in, and the above test is repeated till the paper is coloured hardly perceptibly, or not at all. Each cubic centimetre of the arsenite solution indicates 1 per cent, available chlorine. (For sampling of bleach, cf. Appendix.) Another very accurate method, requiring no standard solution, 160 THE TECHNICAL CHEMISTS' HANDBOOK consists in decomposing the bleaching powder by hydrogen peroxide in a nitrometer or gas-volumeter (Lunge, S.C.I., 1890, 22). 2. Comparison of the Percentage, of Bleaching Powder with the French (Gay-Ltissac) Degrees. — The latter are understood to mean the number of litres of chlorine gas at 0° 0. and 760 mm. pressure which can be given oflf by 1 kilogram of bleaching powder. The oxygen given oflf in -the hydrogen peroxide method (cf. last paragraph) shows this directly. French Per cent. French Per cent. French Per cent. French Per cent. Degrees. ChiOTine. Degrees. Chlorine. Degrees. Chlorine. Degrees. Chlorine. 63 20-28 81 26-07 99 31-87 116 37-34 64 20-60 82 26-40 100 32-10 117 37-66 65 20-92 83 26-72 101 32-51 118 37-99 66 21-25 84 27 04 102 32-83 119 38-31 67 21-57 85 27-31 103 33-16 120 38-63 68 21-89 86 27-36 104 33-48 121 38-95 69 22-21 87 28-01 105 33-80 122 39-27 70 22-55 88 28-33 106 34-12 123 39-51 71 22-86 89 28-65 107 34-47 124 39-92 72 23-18 90 28-97 108 34-78 125 40-24 73 23-50 91 29-29 109 35-09 126 40-56 74 23-82 92 29-62 110 35-41 127 40-88 75 24-14 93 29-94 111 35-73 128 41-20 76 24-47 94 30-26 112 36-05 129 41-63 77 24-79 95 30-63 113 36-38 130 41-85 78 25-11 96 30-90 114 36-70 131 42-17 79 25-40 97 31-23 115 37-02 132 42-49 80 25-75 98 31-55 3. Carbon Dioxide in Bleaching Powder or Bleach Liqvors by Lunge and Rittener's Process. — The same apparatus is employed as that described later on for sodium carbonate solutions (p. 171), and the operation is carried out in the same way, but no aluminium must be used in this case for expelling the gases, but 2 or 3 c.c. of a 3 per cent, solution of hydrogen peroxide which during the final boiling gives out oxygen gas. Employ only so much of the substance that not more than 50 or 60 c.c. of gas (COj and Clj) is formed ; read off the volume of the gases=c in the Bunte burette, charged with concentrated sodium chloride solution, after allowing twenty minutes for cooling, and after putting the level-bottle in the proper position. Introduce into the burette funnel an excess of decinormal arsenic solution =d c.c. ; run this slowly into the burette, so that it forms a layer above the salt solution ; wash the funnel two or three times with a few c.c. of water ; shut off the connection with the level-bottle, BLEACHING POWDER, ETC. 161 shake for two minutes ; run into tlie burette so mucli of a 30 per cent, solution of sodium hydroxide that, on shaking, no more will run in ; read off the volume of gas = b. The figure c — b, or, after reduction to 0° and 760 mm. Cj - fej. indicates the absorbed c.c. CO2+CI2. Now run the contents of the burette into a flask, wash the burette with water, add to the whole an excess of NaHCOs, and titrate with decinormal iodine; the c.c. used=e. Since 20,000 c.c. ^ arsenic solution indicate 22,030 c.c. Clj, we have had in the burette. 22030 20000 and together with this, X {d-e) c.c. chlorine. 22030 20000 {d-e)cc. CO2. 4. Testing the Atmosphere of the Chambers for Chlorine before opening them.^-ln England a maximum of 5 grains chlorine per cubic foot ( = 11 '5 g. per cubic metre) is prescribed before the chamber may be opened. This is ascertained by the appar- atus, Fig. 15. A is a rubber pressure ball holding about 100 c.c, B a hole in its mouthpiece, D a glass tube reaching nearly to the bottom of the glass jar E- its lower end is contracted so that only a thin needle can pass through. E is charged with 26 c.c. of a solution, so prepared that ten deliveries of the bulb indicate 2^ grains (or five de- liveries 5 grains^ chlorine per cubic foot. It is prepared by dissolving 0'3485 g. arsenious acid in sodium carbonate solution, neutral- ising with sulphuric acid, adding 25 g. potassium iodide, 5 g. precipitated calcium carbonate, 6 to 10 drops liquor ammonise, and diluting the whole to 1 litre. To the 26 c.c. of this solution add a little starch solution, introduce the outer end of D into the bleaching-powder chamber 2 feet above the bottom, compress A and cTose the hole B by a finger, whereupon the pressure on A is relieved. By the expansion of the rubber ball A chamber air is aspirated into the liquid contained in E. Note the number of times the ball A must be employed as de- scribed, before the liquid is coloured by the separation of iodine. According to the prescribed limit, this number should be at least 5. Fig. 15. 162 THE TECHNICAL CHEMISTS' HANDBOOK G. — Deacon Process. 1. Proportion of ^G\ and CI in the Gases. — Aspirate 5 litres of gas, issuing from the decomposer, placing the apparatus as near to the outlet of the decomposer as possible, and absorb the hydrochloric acid and chlorine in a solution of caustic soda, sp. gr. 1'075, of which about 250 c.c. are distributed into two or three absorbing-bottles. The time of absorption ought to agree with the tiiue occupied by the charge in the saltcake pan. Unite the contents of the several bottles and dilute to 500 c.c. (a) Take 100 c.c. of this solution, and add it gradually to 25 c.c. of an iron solution (prepared and standardised as directed on page 155) in a flask as shown in Fig. 13, p. 155, and heat to boiling. Allow to cool, dilute with 200 c.c. of water, and titrate with seminormal permanganate solution. Say it required y c.c. Suppose that when standardising the iron solution 25 c.c. of iron solution required x c.c. (6) Take 10 c.c. of the solution to be tested, add a little solution of sulphurous acid, acidify with dilute sulphuric acid ; if it does not smeU of sulphurous acid, add a little more. Heat to boiling. When cool, add, if necessary, a few drops of permanganate to oxidise any sulphurous acid in excess. Neutralise with pure carbonate of soda, dilute with water, and after adding a few drops potassium chromate, titrate with decinormal silver solution. Suppose it requires z c.c. of silver sodium. Then 50a! - y is the percentage of hydrochloric acid decomposed, and 44.94 + 5^ equals the amount of air present for every volume of hydrochloric acid. If any other volume, /, of gas instead of 5 litres be employed, the constant 44'94 becomes 1 60x0003647 assuming that the other directions are strictly followed, and that 1 litre of hydrochloric acid weighs r639 g. at 15° C. at 760 mm. pressure. 2. Carbon Dioxide. — Pass 20 litres of the gas, from which the HCl has been removed by water, into an ammoniacal solution of barium chloride, heat this finally, filter the BaCOs and estimate BLEACHING POWDER, ETC. 163 this by igniting, or by converting it into BaSOj, of which 1 g. =0-1885 g. CO2. Cf. also below, sub H. 3. Steam. — Pass the gas through a weighed tube, containing pumice moistened with strong sulphuric acid, and before reweigh- ing remove the other gases by a current of air. H. — Electrolytic Chlorine. Exxmiination for Carbon Dioxide. — Chlorine gas produced by means of gas-caroon electrodes may contain up to 12 per cent, carbon dioxide. This COj is estimated by Ferchland's process, as modified in Lunge's laboratory. A dry Bunte burette, the content of which (from tap to tap=t)) is exactly known, is filled with the chlorine by passing this through for some time, the gas passing in from below, so as to rise regularly below the lighter air. When filled with the chlorine gas under atmospheric pressure, the burette is fixed in a clamp in a vertical position, and a level tube is attached by means of a strong rubber tube, filled with mercury to the bottom tap, which has a single bore. The rubber tube must be entirely filled with mercury, so that no air can get into the burette, and it is secured against slipping off by iron wire. When the bottom tap of the burette is opened, mercury enters into the burette and absorbs the chlorine, at first pretty quickly, but later on its surface is covered by a pellicle, which precludes further action. Then the bottom tap is closed, and by agitating the burette the complete absorption of the chlorine is effected. The sides of the burette are thereby covered with a non-transparent layer, and a mixture of mercurous chloride and mercury floats on the top of the mercury, which prevent reading off the volume. When the absorption of the chlorine is finished, open the bottom tap, put the level of the mercury approximately equal in the burette and the level tube, and allow ten or fifteen -minutes for the equalisa- tion of the temperature. Now put 1 c.c. saturated solution of sodium chloride into the top beaKer, and allow this to enter the burette by lowering the level tube. This causes the pulverulent mixture on the top of the mercury to subside, and an easily read- able surface to be formed. Then adjust the levels for atmospheric pressure, as described in the case of the nitrometer (p. 137) and read the volume of gas=a. Now introduce a little concentrated solution of potassium hydroxide through the funnel into the burette, absorb the CO3 by shaking, re-establish atmospheric pressure, and read the new volume of gas =6. The formula — — ^ shows the percentage of CO2 in the crude chlorine gas. No correction for vapour tension of water need be made in this case, if concentrated solutions have been used. 164 THE TECHNICAL CHEMISTS' HANDBOOK I. — Chlorate of Potash. 1. Chlorate Liquors contain calcium chlorate and chloride, but these are calciilated as potassium salts for the sake of con- venience. (a) Chlorate is estimated both in order to check the work and to calculate the necessary addition of KCl. Measure 2 c.c. of liquor in an accurate pipette, run it into a flask (Fig. 13, p. 155), add a little hot water and one drop of alcohol, boU (without the valve) tin all smell of chlorine and the pink colour have dis- appeared, allow to cool, add 25 c.c. of the strongly acid ferrous sulphate solution (c/. p. 155, and requiring a c.c. of seminormal permanganate), close the flask with its valve, and boU for ten minutes. After cooling, titrate with seminormal permanganate. The number of cubic centimetres required to produce a faint pink =6. The liquor then contains calcium chlorate equivalent to 5"105 (a-b) g. KCIO3 per litre, and it will theoretically require an amount of 3" 106 (a-b) g. of pure KCl per litre. (b) Chloride is estimated in order to check the work, and is therefore calculated as KCl, although present as CaCl2. Treat 1 c.c. of liquor as above, to destroy the free chlorine and pink colour, allow to cool, add a little neutral potassium chromate, and titrate with decinormal silver nitrate (as described p. 146). Each cubic centimetre of the latter indicates chloride equivalent to 7-456 g. KCl per litre. 2. Commercial Chlorate of Potash is only tested for chlorides, calculated as KCl. As their quantity is very small, it is advisable to dissolve 50 g. of the salt in water absolutely free from chlorine, and to test with decinormal silver nitrate, as in 1 (b). Each cubic centimetre of this solution =0'007456 g. KC1=0"015 per cent. KCl. E. — Bleach Liquors. These are tested like Bleaching Powder, p. 159. Electrolytic Bleach Liquor, see p. 193. BLEACHING POWDER, ETC. 165 L.— PRESSURE AND SPECIFIC GRAVITY OF LIQUID CHLORINE. (Knletseh). Temperature. Pressure. specific Gravity. ^r^^S!'* -88° 37-5 mm. Hg. -85 45-0 -80 62-5 1-6602 -75 88-0 1-6490 -70 118 1-6382 -65 159 1-6273 -60 210 1-6167 -55 275 1-6055 0-001409 -50 350 1-5945 -45 445 1-5830 -40 560 1-5720 -35 705 1-5589 -33-6 760 1-5575 -30 l'20atm. 1-5485 -26 1-50 „ 1-5358 -20 1-84 „ 1-5230 -15 2-23 „ 1-5100 0-001793 -10 2-63 „ 1-4965 - 5 3-14 „ 1-4830 ± 3-66 „ 1-4690 + 5 + 10 4-25 „ 4-95 „ 1-4548 1-4405 1 0-001978 + 15 + 20 5-75 „ 6-62 „ 1-4273 1 -4118 1 0-002030 + 25 + 30 7 -63 „ 8-75 „ 1 -3984 1-3815 1 0-002190 + 35 + 40 9-95 „ 11-50 „ 1 -3683 1-3610 1 0-002260 50 60 14-70 „ 18-60 „ 1 -3170 1-2830 1 0-002690 70 SO 23-00 „ 28-40 „ 1-2430 1-2000 1 0-003460 90 34-60 „ 100 41-70 „ 110 50-80 „ 120 60-40 „ 130 71-60 ., 146 93-50 „ Critical Point 166 THE TECHNICAL CHEMISTS' HANDBOOK V. SODA ASH MANUFACTURE BY THE LEBLANC PROCESS. A. — Ra-w Materials. 1. Saltoake.— ((7/. p. 147.) 2. Limestone or Chalk, for mixing. (a) Insoluble.— {Gf. p. 157.) (b) Lime (+MgO).— (P. 158.) (c) Magnesia (only in limestones containing muci magnesia). — (P. 156.) 3. Mdong Coal (slack). (a) Moisture.— (?. 93.) (b) Fixed Carbon.— {Y. 93.) _(c) Ash (p. 93). — In the case of unknown descriptions of coal it is not sufficient to estimate the total percentage of ash, but the latter should be analysed, and silica, alumina, and ferric oxide estimated according to the methods for the analysis of silicates. (d) Sulphwr.—(P. 94.) (e) Nitrogen is estimated by igniting with soda-lime and absorb- ing the ammonia formed in standard sulphuric acid, according to the method employed in organic analysis. B. — Black-Ash. Digest 50 g. of the finely powdered average sample with 480 c.c. of water at 45° C, which have been previously freed from CO, and O by boiling and cooling down in a corked bottle. This will produce 500 c.c. of liquid. Shake at once and afterwards fre- quently, at least during two hours. The following tests are made partly with the muddy mixture, partly with the clear portion ; the former ones must be made to begin with. 1. Tests made with the Muddy Mixtuee. — Each time before taking out a sample, the flask is thoroughly shaken up, and before the deposit settles again a sample is taken by means of a 5 c.c. pipette, with a short and somewhat wide outlet (to prevent obstruction by the mud). The mud outwardly adhering IS washed oflF, the contents of the pipette are run out into a beaker, and the mud adhering to the inside of the pipette is washed into the same beaker. (a) Free Lime (or its equivalent of sodium hydroxide) is estimated by adding to 6 c.c. of the mixture an excess of SODA ASH MANUFACTURE 167 barium chloride solution, as well as a drop of phenolphthalein solution, and titrating with ^ normal oxalic acid, till the red colour has just vanished. Each c.c. of the acid=0005607 g. CaO. (b) Total Lime. — 5 c.c. of the muddy mixture are put into a flask, a few c.c. of concentrated hydrochloric acid are added, and the whole is boiled till all the gases have been expelled. Cool down a little, add a drop of methyl orange solution, and neutralise exactly with sodium carbonate, i.e. till the red colour has just gone. Then add 30 c.c. of J normal sodium carbonate solution, measured exactly, and heat to boiling, to precipitate all the lime as CaCOj (together with any ferric oxide, alumina, and magnesia, the quantity of which is too insignificant to be regarded for this test). Wash the jjhole into a 200 c.c. flask, fill up to the mark, take 100 c.c. of the clear liquid, and titrate back with ^ normal hydrochloric acid. Deduct the c.c. used x 2 from 30 ; the differ- ence X 0'005607 = total lime, or x 0'010007 = calcium carbonate. {N.B. — These tests cannpt be expected to give very accurate results, owing to the almost insurmountable difficulty of obtaining a real average sample of black-ash ball. This, however, applies to all tests made with black-ash.) 2. Tests made with the Clear Portion. — After having made all the tests described under 1, allow the mixture to settle down in the well-corked flask, and take samples of the supernatant, clear liquid for the following tests : — (a) Available Alkali cmd Sodium Carbonate. — 10 c.c. (=1 g. black-ash) is titrated cold with hydrochloric acid and methyl orange. This indicates the total available alkali, i.e., NajCOs, NaOH, and NajS. (The small quantity of alumina and silica present causes no appreciable error.) By deducting the quantities found in tests Nos. 2 and 3 the quantity of sodium carbonate is found, viz., 0'05300 g. for each cubic centimetre of normal HCl. It is, however, expressed, like all other sodium compounds, in terms 'of NajO, by multiplying the cubic centimetres of normal acid used by 0-03100. (b) Caustic Soda is estimated by adding to 20 c.c. of solution, contained in a 100 c.c. flask, an excess of barium chloride (10 c.c. of a 10 per cent, solution of BaCl2, 2H2O, will always more than suffice for this), adding boiling water up to the mark, shaking up, and corking the flask. After a few minutes the precipitate settles. Take out 50 c.c. of the clear portion, without filtering,* and titrate with normal hydrochloric acid. When employing methyl orange as indicator, the liquid must be cooled first and the titration must be made slowly, with constant shaking. Each cubic centimetre of the standard acid indicates 0'04001 g. of NaOH in 1 g. of black-ash =0'03100 g. NajO, but sodium sulphide is also included. * The filter paper absorbs an appreciable portion of barium salt. 168 THE TECHNICAL CHEMISTS' HANDBOOK (c) Sodium Sulphide.— D^inA^ 10 c.c. of solution to about 200 c.c, employing water freed from oxygen by boiling, acidulate with acetic acid, and titrate quickly with iodine solution, using starch as an indicator. When employing a decinormal iodine solution (12'692 g. I per litre), each cubic centimetre indicates 0'003904 g. Na2S ( =0'0031 00 g. NajO). A solution containing 3"251 g. I per litre would indicate O'OOl g. NagS per cubic centimetre. In the former case the number • of cubic centimetres of decinormal solution divided by 10 can be deducted at once from the acid employed in test No. 1, whereby the sulphide is eliminated from the alkali test. Other sulphur compounds (except sulphate) need not be taken account of in fresh black-ash. (d) Sodium Chloride. — Neutralise 10. c.c^of the liquor as accurately as possible with nitric acid, preterably by adding exactly as many cubic centimetres of standard nitric acid (63'02 g. HNO3 per litre) as had been employed in test No. 1 . Boil till all HgS has been expelled, filter from any suljjhur precipitated, add a little neutral potassium chromate, and titrate with silver solution (as described p. 146). Each cubic centimetre of deci- normal silver solution indicates 0'005846 g. NaCl. A solution con- taining 2'9061 g. AgNOj per litre corresponds to O'OOl g. NaCl per cubic centimetre. (e) Sodium Sidphate. — Acidulate 10 c.c. with a very slight excess of HCl, boil, add barium chloride, filter, wash, and ignite the precipitated BaS04. Since the quantity is very small, it can be washed with hot water on the filter itself, which is then placed in the moist state in a platinum crucible and ignited. Each part of BaS04= 0-6086 NajSOi. (f) Prepare an average sample of all batches by pouring a certain quantity of the liquor belonging to each batch into a common vessel ; carbonate this by passing OO2 through it, filter, evaporate the jiltrate to dryness, and estimate Na2C03, Na2S04, and NaCl in the residue. C— Tank Waste (Vat Waste). Take a large, really representative, average sample, which should be kept protected from air, and of which 50 g. should be weighed out quickly and in the moist state. Drying in contact with air would considerably change its composition. Moist tank waste may be assumed, without any great error, to contain 40 per cent, of water. Digest the above 50 g. waste with 490 c.c. water of 40° C, which will yield 500 c.c. of liquid. 1. Available Soda (NajCOs, or NagS).— Take 100 c.c. of the liquor, pass into it a current of well-washed carbon dioxide, heat the liquid to boiling, bring up the volume again to 100 c.c, pour through a dry filter, and titrate 50 c.c. of the clear portion with SODA ASH MANUFACTURE 169 decinormal hydrochloric acid, of which each c.c. will indicate O'OOSIOO g. NagO, or, in this case, 0'0620 per cent. NagO on the moist waste. 2. Total Soda (mcltmve of Insoluble Sodium, Salts). — Heat 17'71 g.* tank waste in a porcelain or iron dish with sulphuric acid of specific gravity 1'5, till all has been decomposed and converted into a stiflf paste, evaporate to dryness, heat till all free sulphuric acid has been driven off, add hot water, scrape out the mass, and put it into a 250 c.c. cylinder. Neutralise any free acid left, and precipitate any magnesia present by adding pure milk of lime (obtained from ordinary slaked lime by pouring off the first water, which may contain some alkali), fill up to the mark, allow to settle, take out 50 c.c. of the clear liquor, add 10 c.c. of saturated baryta water, pour the mixture through a dry filter, take 50 c.c. of the filtrate, precipitate all baryta by passing through the liquid COj and boiling, filter, and titrate the filtrate with decinormal hydrochloric acid. Each cubic centimetre of this will indicate O'l. per cent, of NajO in the waste, taking into account its bulk. 3. Total and Oxidisdble Sidphv/r. — Boil 2 g. of the waste with hydrochloric acid, filter, wash with dilute HCl, neutralise the filtrate almost completely by adding sodium carbonate, precipitate with barium chloride, filter, wash, and ignite the barium sulphate. From this the sulphur present as sulphate is calculated (a). Another sample of 2 g. waste is oxidised by a strong bleaching- powder solution and hydrochloric acid, or by a solution of bromine in strong hydrochloric acid. When a strong smell of chlorine persists, all S is oxidised to sulphuric acid. Filter and estimate the SO4H2 in the filtrate. This indicates the total sulphur (6). The difference 6 — a is the oxidisable sulphur, i.e. the theoretically recoverable maximum of sulphur in the waste. D. — Tank Liquor (Vat Liquor). Vat liquor is tested while hot, or else it is kept at about 40° C, to prevent crystallisation. Take out only small samples (2 to 5 c.c.) with an accurate pipette. This greatly facilitates the work. l._ Sodium Carbonate. — Titrate 2 c.c. with standard hydro- chloric acid. When employing methyl orange as indicator, first add some cold water. From the volume required deduct that found in test No. 2, and one-tenth of that in test No. 3. 2. Sodium Hydroxide (estimated as on p. 167). 3. Sodium, Sulphide is estimated by decmormal iodine solution * Thia amount is correct, not 18-6 g., as calculation would seem to show, because an allowance must be made for tlie biilk of tbe insoluble residue in the measuring- vessels. 170 THE TECHNICAL CHEMISTS' HANDBOOK (as on p. 168). The error caused by other sulphur compounds is hardly appreciable, and for practical purposes of no consequence. In any case this test must be made in order to correct test No. 1. 4. Sodium Sulphate (as on p. 168). 5. Total SvlpKwr. — Oxidise the liquor with bleaching jjowder and hydrochloric acid (as described, C. 3, p. 169), and precipitate with barium chloride. 6. Sodium Chloride (as on p. 168). 7. SodivMi Ferrocyanide. — Acidulate 20 c.c. of liquor (or more) with HCl, and add strong bleaching-powder solution from a burette, constantly agitating. From time to time mix a drop of the" mixture on a white slab with a drop of dilute ferric chloride solution, free from ferrous chloride. When no more Prussian blue is formed, but the mixture of both drops turns brown, aU is oxidised, hence also all ferrocyanide is tujned into ferricyanide. A drop of bleach solution in excess does no harm, but if too much excess ha^ been used, or if too much liquor has been lost by taking out test drops, a fresh sample is taken out, which can then be oxidised by running the requisite quantity of bleach liquor from the burette without losing much by making the drop-tests. This method gives quicker and more accurate results than adding an excess of bleach and driving out the chlorine by heating, in which case some ferricyanide may be decomposed. The oxidised liquor is titrated with decinormal copper solution, containing 3'1785 g. Cu. or 12"486 g. crystallised cupric sulphate per litre, which precipitates yellow Cu3Fe3Cyi2. From time to time test a drop of the liquid by bringing it together on a porcelain slab with a drop of a dilute ferrous sulphate solution. So long as a blue colour is produced by the action of FeS04 on NaaFeC^ye more copper solution is added, till the test on the slab does not turn blue or grej^ but reddish. Now no more NasFeCyo is present, and the FeSOi on the slab reduces the yellow copper ferri- cyanide to red ferrocyanide. The first sensible reddening must be taken as the final reaction, although, it vanishes after a short time. According to theory, each cubic centimetre of the copper solution ought to indicate O'OIOIS g. NaiFeCyc ; but direct experi- ments (Chem. Ind., 1882, p. 79) have shown this not to be the case. Too httle copper solution is employed, and each cubic centimetre of this must therefore be regarded as equal to 0'0123 g. NasFeCyo, or, still better, the copper solution must be standardised by pure potassium ferrocyanide. 8. Silica, Alumina, and Ferric Oxide (PameU). — Supersaturate 100 c.c. of liquor with HCl, boil, add a large quantity of ammonium chloride and ammonia in excess, and boil till all smell of NH3 has ceased. The precipitate settles easily, and can be well washed. On washing with hot water it turns intensely blue (owing to the formation of Prussian blue ?) ; on igniting it leaves SiOj, AljO^, and FcoOj. SODA ASH MANUFACTURE 171 9. A large sample of tte liquor is carbonated by passing CO2 tlirough it; it is then filtered, evaporated to diyness, and the residue tested for available alkali, NajSOj and KaCl. B. — Carbonated Liquor. This is tested like tank liquor (No. D) ; also for bicarbonate. This is done with sufiBcient accuracy for practical purposes as follows : — Titrate 10 c.c. of liquor, without diluting it, in the cold with normal hydrochloric acid, em- ploying phenolphthalein as indi- cator, until this is decolorised. The temperature should not be much above 0°. The c.c. of ^ HCl used =a. Now add a drop of methyl orange and more acid, until the colour changes ; the c.c. -^ HCl used for this = b. Then b-a indi- cates the bicarbonate, 2a the soda present as NajCOs, a+b the total soda. For other methods, see "Bicarbonate," p. 186. The most accurate and at the same time the quickest method for estimating carbon dioxide, both in small and in large quantities, is that of Lunge and Kittener {Z. angew. Chem., 1906, p. 1849). Their apparatus is shown in Fig. 16. The small flask B, holding about 30 C.C., is provided with a tap funnel C and a long capillary D, which is connected with the lateral capillary of the two-way tap E of the gas-burette A. D should be cut off at the lower surface of the rubber stopper of B. Introduce so much substance (solid or liquid) into B that it cannot yield more than 80 c.c. CO2; also 15 c.c. of very fine aluminium wire, rolled up in a spiral. Then close B and connect D with tap E of burette A. This is an ordinary Bunte burette ; as usual, it is divided in c.c, beginning below the tap E with 100, going downwards to B, then again to - 10 c.c, leaving a few c.c. of undivided space down to the tap F. A level-bottle, G, can be connected with F in the ordinary manner ; it contains a* saturated solution of sodium chloride. At the beginning of the operation F is not connected with G, but with a water-pump which is turned on for two or three minutes, in ordet to evacuate the apparatus B - D - A. F is then closed 172 THE TECHNICAL CHEMISTS' HANDBOOK and the capillary below this tap connected with the rubber tube of the level-bottle G. By cautiously opening F, a little of the salt solution is allowed to pass from G through F, till it appears just above this tap in the capillary space of A. This is done in order to check any leak at F. If a solution is to be tested which is not previously contained in flask B, it is poured into funnel C, and by cautiously opening the tap it enters into B. Kinse C twice or thrice with a little water, and then introduce through C enough hydrochloric acid to decompose the carbonate and dissolve the aluminium wire. If B contains initially a solid substance or a solution, the acid is of course run in directly through C. In any case this is done drop by drop, to avoid a violent reaction. When the reaction slackens, heat B gently, until the aluminium is dissolved, and then bring the solution to the boil, until drops of water condense in E. Now close E and allow water to enter through C, to completely fill the flask B and the capillary C. If a few small bubbles of gas should remain in C, they are transferred to A by cautiously opening E for a few moments. Next detach the capillary D from E, and wait twenty to twenty-five minutes, so that the gas in A is cooled down to the temperature of the outer air. Read the thermometer H, attached to the upper part of A by means of rubber rings, note also the barometer, cautiously open tap E, until the liquid in G and A stands at the same level, close F, and read the volume of gas in A, preferably by means of a Gockel reading-screen. Now run a strong solution of caustic soda (1 : 2 water) through E into A, without taking notice of any precipitation of calcium carbonate, which will take place in A, if a solution of impure common salt has been used in the level-bottle G. Close E, shake A, in order to promote the absorption of COg, adjust the liquid in G and A to the same level, read off the volume in A, and introduce more caustic soda solution until this causes no further contraction of the volume of gas. The difference between the first readiug a and that taken after absorption of the 002=6 shows the volume of the CO2 originally present, which is reduced to 0° and 760 mm. in the usual way. Of course regard must be had to the fact that the tension of a saturated NaCl solution is less than that of pure water; for ordinary temperatures it may be put =80 per cent, of the tension of pure water (Table 24, p. 53), so that, e.g., at 15° C. it will be 12 mm. instead of 15 mm. If you call the volumes of gas, reduced to the normal state, a^ and 61 and the weight (or volume) of substance employed m, its percentage of CO2 is : — 0-19768 (g^- 6') Instead of absorbing the COj in the burette A, as described, it SODA ASH MANUFACTURE 173 miglit be transferred, by raising G, into a Hempel's or Dreh- schmidt's absorption-pipette, attached to a. This pipette is filled ■with caustic soda solution. After the CO2 has been absorbed, the remaining gas is retransferred to A, by raising G. E is then closed, the liquid adjusted to the same level in A and G, and the volume of the gas read and reduced to normal conditions as above. F. — Mother Liquor. This is tested like uncarbonated tank liquor, p. 169. But in this case it is necessary to estimate sulphide, sulphate, sulphite, and thiosulphate in the presence of one another. The most con- venient method for this purpose is that of Lunge and Smith {Chem. Ind., 1883, p. 301), which is as follows : — (a) Sulphate is estimated by displacing the air in the flask by CO2 (to prevent oxidation by air), heating, acidulating, and pre- cipitating with BaCl2. (b) Other Compov/nds of Stdphur. —In a second sample deter- mine the consumption of decinormal iodine solution, after diluting with water free from air and acidulating with acetic acid. (c) To a sample, four times the amount of (b), add zinc acetate or cadmium carbonate, in order to remove the NajS, dilute it to a known volume, allow to settle, and take a quarter of the clear liquid for each of the following tests : — (1) The consumption of decinormal iodine =M. (2) To another quarter add, v?ithout acidulating it, a large excess of permanganate solution of the value W (see below), the solution to be tested being run into the permanganate solution ; then an acid solution of ferrous sulphate, of known value against KMn04, is added in excess, and the excess is titrated back by permanganate, The total permanganate solution used, less that corresponding to the ferrous sulphate, is called N. (The value W signifies the quantity of permanganate solution used in accordance with the equation : — SNaaSaOa + SKMnOi + HgO = 3Na2S04 + 3K2SO4 + SMnOa + 2K0H, which is found by calculation, or else experimentally by titration of pure sodium thiosulphate.) If we call the sulphur of thiosulphate S, that of sulphate s, we have : — S = ■J-(8WN-0-0064M) « = 2WN-2S. By deducting M from the result of the original iodine titra- tion (b) you find the amount of NagS. Another method for the same purpose, by Richardson and Ackroyd, has been pubUshed in Jow-n. Soc, Chem. Ind., 1896, p. 172. 174 THE TECHNICAL CHEMISTS' HANDBOOK G. — Tables. SPECIFIC GRAVITIES OF SOLUTIONS OF SODITJM CARBONATE AT 15° O. Fer cent. by weight. 1 cubic metre contains kilog. Specific Degrees Degrees gravity. TwaddeU. Baume. NaaOOa. ^.^^a^^- NasCOs. NaaCOg, 10 aq. 1-000 0-00 0-00 0-00 0-00 1-005 1 0-7 0-45 1-21 4-52 12-16 1-010 2 1-4 0-91 • 2-46 9-19 24-85 1-015 3 2-1 1-39 3-75 14-11 38-06 1-020 4 2-7 1-90 5-13 19-38 52-33 1-025 5 3-4 2-35 6-34 24-09 64-99 1-030 6 4-1 2-82 7-61 29-05 78-38 1-035 7 4-7 3-27 8-82 33-84 91-29 1-040 8 5-4 3-74 10-09 38-90 104-94 1-045 9 6-0 4-21 11-36 43-99 118-71 1-050 10 6-7 4-70 12-68 49-35 133-14 1-055 11 7-4 5-17 13-95 54-54 147-17 1-060 12 8-0 5-65 15-24 59-89 161-64 1-065 13 8-7 6-15 16-69 65-50 176-68 1-070 14 9-4 6-63 17-89 70-94 191-42 1-075 15 10-0 7-08 19-10 76-11 205-33 1-080 16 10-6 7-56 20-40 81-65 220-32 1-085 17 11-2 8-03 21-67 87-13 235-12 1-090 18 11-9 8-48 22-88 92-43 249-39 1-095 19 12-4 8-90 24-01 97-46 262-91 1-100 20 13-0 9-31 25-12 102-41 276-32 1-105 21 13-6 9-80 26-44 108-29 292-16 1-110 22 14-2 10-27 27-71 114-00 307-58 1-115 23 14-9 10-75 29-00 119-86 323-35 1-120 24 15-4 11-22 30-27 125-66 339-02 1-125 26 16-0 11-67 31-49 131-29 354-26 1-130 26 16-5 12-17 32-83 137-62 370-98 1-135 27 17-0 12-64 34-10 143-46 387-04 1-140 28 17-7 13-08 35-29 149-11 402-31 1-145 29 18-3 13-60 36-42 154-58 417-01 1-150 30 18-8 13-94 37-61 160-31 432-52 1-165 31 19-3 14-34 38-69 165-63 446-87 SODA ASH MANUFACTURE 175 2. SPBCIPIC GRAVITIES OP CONCENTRATED SOLUTIONS OP SODIUM CARBONATE AT 80° C* Per cent. by weight. 1 cubic metre contains kilog. Speciflo gravity at 80'. Degrees Twaddell. Degrees Baum6. 1 NajCOs. NagCOs, 10 aq. NaaCOs. NajCOs, 10 aq. 1-310 62 34-2 28-08 75-76 367-85 S92-46 1-305 61 33-7 27-66 74-63 360-96 973-92 1-300 60 33-3 27-25 73-52 354-25 955-76 1-295 59 32-8 26-84 72-41 347-58 937-71 1-290 58 32-4 26-42 71-28 340-82 919-51 1-285 57 32-0 26-00 70-15 334-10 901-43 1-280 56 31-5 25-60 69-07 327-68 884-10 1-275 55 31-1 25-18 67-94 321-05 866-24 1-270 54 30-6 24-74 66-75 314-20 847-73 1-265 53 30-2 24-28 65-51 307-14 828-70 1-260 52 29-7 23-85 64-35 300-51 810-81 1-255 51 29-3 23-43 63-21 294-05 793-29 1-250 50 28-8 23-03 62-14 287-88 776-75 1-245 49 28-4 22-63 61-06 281-74 760-20 1-240 48 27-9 22-22 59-95 275-53 743-38 1-235 47 .27-4 21-80 58-82 269-23 726-43 1-230 46 26-9 21-37 57-66 262-85 709-22 1-225 45 26-4 20-96 56-55 256-76 692-73 1-220 44 26-0 20-55 55-44 250-71 676-37 1-215 43 25-5 20-12 54-28 244-46 659-60 1-210 42 25-0 19-67 53-07 238-01 642-15 1-205 41 24-5 19-26 51-96 232-08 626-12 1-200 40 24-0 18-83 50-80 225-96 609-60 1-195 39 23-5 18-42 49-70 220-42 594-22 1-190 38 23-0 18-00 48-56 214-20 677-84 1-185 37 22-5 17-65 47-35 207-97 561-10 1-180 36 22-0 17-09 46-11 201-66 544-10 1-175 35 21-4 16-62 44-84 195-29 526-87 1-170 34 20-9 16-16 43-60 189-07 510-12 1-165 33 20-3 15-70 42-36 182-91 493-49 1-160 32 19-8 15-25 41-14 176-90 477-22 1-155 31 19-3 14-84 40-04 171 -40 462-46 1-150 30 18-8 14-42 38-91 165-83 447-47 1-145 29 18-3 14-02 37-83 160-53 433-15 1-140 28 17-7 13-61 36-72 155-15 418-61 * ThiB temperature has been apecially chosen, because the higher ooncentrationa of sodium sarbonate cannot exist in solution at lo'vrer temperatures. 176 THE TECHNICAL CHEMISTS' HANDBOOK 8. INPLTJENOB OF TEMPERATURE ON THE SPECIFIC O'C. 5'. 10°. 15°, 20°. 26° 30°. 85°. 40°. 45° 60°. 1-285 1-282 1-279 1-276 1-273 ... 1-274 1-271 1-267 1-265 1-262 ... ' ... 1-263 1-260 1-257 1-254 1-251 ... ... 1-252 1-250 1-247 1-244 1-240 1-241 1-239 1-236 1-233 1-230 1-240 1-238 1-236 1-234 1-232 1-230 1-227 1-224 ... ... 1-230 1-228 1-225 1-223 1-221 1-219 1-216 1-213 ... ... 1-220 1-218 1-215 1-213 1-210 1-208 1-205 1-201 ... ... ... 1-210 1-208 1-206 1-204 1-201 1-199 1-196 1-192 ... 1-200 1-198 1-196 1-194 1-192 1-189 1-186 1-183 1-198 1-195 1-193 1-190 1-188 1-186 1-184 1-182 1-179 1-176 1-173 1-188 1-185 1-183 1-180 1-178 1-176 1-174 1-172 1-169 1-166 1-163 1-177 1-174 1-172 1-170 1-168 1-166 1-164 1-162 1-160 1-157 1-154 1-166 1-164 1-162 1-160 1-158 1-156 1-154 1-152 1-150 1-148 1-145 1-156 1-154 1-152 1-150 1-148 1-146 1-144 1-142 1-139 1-136 1-134 1-146 1-144 1-142 1-140 1-138 1-136 1-134 1-132 1-129 1-126 1-123 1-136 1-134 1-132 1-130 1-128 1-126 1-124 1-122 1-120 1-117 1-114 1-126 1-124 1-122 1-120 1-118 1-116 1-114 1-112 1-110 1-107 1-104 1-116 1-114 1-112 1-110 1-108 1-106 1-104 1-102 1-100 1-098 1-095 1-106 1-104 1-102 1-100 1-098 1-096 1-094 1-092 1-090 1-088 1-085 1-096 1-094 1-092 1-090 1-088 1-086 1-084 1-082 1-080 1-078 1-075 1-086 1-084 1-082 1-080 1-078 1-076 1-074 1072 1-070 1-068 1-065 1-075 1-073 1-071 1-070 1-069 1-067 1-065 1-063 1-061 1-059 1-056 1-064 1-063 1-061 1-060 1-059 1-057 1-056 1-054 1-052 1-050 1-047 1-053 1-052 1-051 1-050 1-049 1-048 1-046 1-044 1-042 1-040 1-037 1-043 1-042 1-041 1-040 1-039 1-038 1-036 1-034 1-032 1-030 1-027 1-033 1-032 1-031 1-030 1-029 1-028 1-026 1-024 1-022 1-020 1-017 1-023 1-022 1-021 1-020 1-019 1-018 1-016 1-014 1-012 1-010 1-007 1-013 1-012 1-011 1-010 1-009 1-008 1-006 1-004 1-002 1-000 0-997 SODA ASH MANUFACTURE 177 GRAVITIES OF SOLUTIONS OF SODIUM CARBONATE, 66'. 60". 65°. 70". 75'. 80', 86°. 90". 95". 100". 1-270 1-267 1-264 1-260 1-256 1-252 1-247 1-243 1-238 1-234 1-259 1-256 1-253 1-249 1-244 1-240 1-236 1-232 1-228 1-224 1-248 1-245 1-241 1-237 1-233 1-229 1-226 1-222 1-218 1-215 1-237 1-234 1-230 1-227 1-224 1-220 1-217 1-213 1-210 1-206 1-226 1-223 1-220 1-216 1-213 1-210 1-207 1-204 1-200 1-197 1-220 1-217 1-213 1-210 1-206 1-203 1-199 1-195 1-191 1-188 1-209 1-206 1-202 1-199 1-195 1-192 1-188 1-184 1-181 1-178 1-198 1-194 1-191 1-188 1-184 1-181 1-178 1-174 1-171 1-168 1-189 1-185 1-182 1-178 1-175 1-172 1-168 1-165 1-162 1-159 1-179 1-176 1-172 1-168 1-165 1-162 1-158 1-155 1-152 1-149 1-169 1-166 1-163 1-159 1-156 1-153 1-149 1-146 1-143 1-140 1-160 1-166 1-153 1-150 1-147 1-144 1-140 1-137 1-134 1-131 1-151 1-147 1-144 1-141 1-138 1-135 1-131 1-128 1-125 1-122 1-142 1-139 1-136 1-133 1-130 1-126 1-123 1-120 1-117 1-114 1-131 1-128 1-125 1-122 1-119 1-116 1-113 1-110 1-107 1-104 1-120 1-118 1-115 1-112 1-109 1-106 1-103 1-100 1-097 1-094 1-111 1-108 1-105 1-102 1-099 1-096 1-093 1-090 1-087 1-084 1-101 1-098 1-095 1-092 1-089 1-086 1-083 1-080 1-077 1-074 1-092 1-089 1-086 1-083 1-080 1-077 1-074 1-071 1-068 1-065 1-082 1-079 1-076 1-073 1-070 1-067 1-064 1-061 1-058 1-055 1-072 1-070 1-067 1-064 1-061 1-058 1-055 1-052 1-049 1-046 1-062 1-060 1-057 1-054 1-052 1-049 1-046 1-043 1-040 1-038 1-053 1-051 1-048 1-045 1-043 1-040 1-037 1-034 1-032 1-029 1-044 1-041 1-038 1-036 1-032 1-030 1-028 1-025 1-023 1-020 1-034 1-032 1-029 1-027 1-024 1-021 1-019 1-016 1-014 1-011 1-024 1-022 1-019 1-017 1-015 1-012 1-010 1-007 1-005 1-003 1-014 1-012 1-009 1-007 1-005 1-002 1-000 0-997 0-995 0-993 1-004 1-002 0-999 0-997 0-995 0-992 0-990 0-987 0-985 0-983 0-994 0-992 0-989 0-987 0-985 0-982 0-980 0-977 0-975 0-973 M 178 THE TECHNICAL CHEMISTS' HANDBOOK E. — Analysis of Commercial Soda Ash. When merely the available alTcali (alkalimetrical degree) has to be ascertained, it is convenient to weigh out 15"5 g., to dissolve in a 500 c.c. flask, and to take for each test 50 c.c. (in Germany, without filtering ; in England, sometimes with, sometimes with- out). In this case each cubic centimetre of standard acid indi- cates O'OSIOO g. NajO, or just 2 per cent, of available alkali (NajO). The standard acid is normal hydrochloric acid, containing 36"468 g. HCI per litre, and is standardised both with pure sodium carbonate and with silver nitrate. {Gf. Appendix.) The indicator is either litmus (in which case the solution has to be boiled for some time) or more conveniently, methyl orange (which is used with cold solutions). If the percentage of alkali is to be calculated in terms of NaaCOj, as is usual in Germany and other countries, 2"6500 g. is weighed out, dissolved, and titrated (without filtering) with normal hydrochloric acid, each c.c. of which indicates 2 per cent. NajCOa in this case. In Germany the samples are ignited before weighing, and the percentage is always stated for soda ash in this dry state. For a complete analysis of commercial soda ash 50 g. are dissolved in warm water. 1. The Insoluble Residvs is filtered and washed, the filtrate and washings are diluted up to 1 litre, and the following tests are made with this solution. 2. Soditim Carbonate is found by titrating 20 c.c. (equal to'l g. of soda ash) with normal HCI, deducting the amount of No. 3. That of No. 4 is always too small to consider in this case. 3. Sodium Hydroxide is estimated by barium chloride, accord- ing to p. 167. 4. Sodium Sulphide. — 100 c.c. (equal to 5 g. of ash) are titrated with ammoniacal silver nitrate (c/. Appendix), containing 13'818 g.' Ag. per litre, and indicating 0"005 g. Na^S per cubic centimetre. _ Heat the soda liquor to boiling, add ammonia, and run in the silver solution from a burette divided in 3^ c.c, till no further black precipitate of AgjS is produced. In order to observe this more accurately the liquid is filtered towards the end of the operation, and the titration is continued if necessary. This filtration is repeated several times. Each cubic centimetre of silver solution mdicates O'l per cent, of NajS in the alkali. 6. Sodium, Sulphide. — Acidulate 100 c.c. (egual to 5 g. soda ash) with acetic acid, add starch solution, and titrate with iodine till a blue colour appears. A decinormal iodine solution corre- SODA ASH MANUFACTURE ' 179 spends to 0'006304 g. NajSOs per cubic centimetre (in this case 0"126 per cent.). The solution mentioned on p. 169 of 3'251 g. iodine per litre, corresponds to 0'001615 g. NajSOg (in this case 0"0323 per cent.). From this should be deducted the amount corresponding to test No. 4 ; 1 c.c. of the silver solution can be regarded as equal to 1'3 c.c. of the decinormal, or equal to 5'0 c.c. of the weaker iodine solution. 6. Sodium Stdfhate. — Acidulate 20 c.c. of the solution (equal to 1 g. soda ash) with hydrochloric acid, precipitate with barium chloride, as on p. 109, and weigh the BaSOi, of which I'OOO part is equal to 0"6086 part Ka2S04. 7. Sodivm, Chloride. — Neutralise 20 c.c. (equal to 1 g. soda ash) exactly with nitric acid, preferably by adding exactly as many cubic centimetres normal nitric acid from a burette as had been used in test No. 1 ; then add neutral potassium chromate, and titrate with decinormal silver nitrate as described onp. 146. Each cubic centimetre of this corresponds to 0"005846 g. NaCl. 8. Iron. — Neutralise 100 c.c. (equal to 5 g. soda ash) with sulphuric acid free from iron, reduce with zinc free from iron (p. 143), and titrate with -^ normal potassium permanganate, of which each cubic centimetre corresponds to 0'002793 g. Fe, or in this case 0'0559 per cent. Fe. 9. Sodium Silicate is not present in appreciable quantities in ordinary soda ash, but always m the ash recovered from the liquor used in the manufacture of wood " cellulose." It is estimated by acidulating 20 c.c. (equal to 1 g. soda ash) with HCl, filtering the Si02, drying, and igniting. 1 g. SiO2=2'028 g. NagSiOa. 10. Table for comparing French, German, and English Com- mercial Alkalimetrical Degrees. — The French or Descroizilles degrees mean the quantity of real sulphuric acid, SO^Hg, neutral- ised by 100 parts of soda ash. The German degrees express the available alkali in terms of sodium carbonate, NajCOa. In England some works invoice in real per cent, of soda, Na20, as found in the first column of the foUowmg tables. The Newcastle test is based on the equivalent 32 for NajO, or 59'26 degrees for pure Na^COs, and invoices fractions of degrees. [COMMBECIAI AlKALIMETBICAL DeGEEES. 180 THE TECHNICAL CHEMISTS' HANDBOOK FRENCH, QSBMAN, AND SNQLISH COMMBBCIAL AIiKALIUlEiTBICAIi DBOBEBS. Real German New- castls Beal German New- Soda. degrees. French Soda. degrees. French NagO. NaaCOg. -2 degrees. degrees. Na20. NaaCOs. degrees. degrees. 0-5 0-86 0-51 0-79 18 30-78 18-23 28-45 1 1-71 1-01 1-68 18-5 31-64 18-74 29-24 1-6 2-57 1-52 2-37 19 32-49 19-25 30-03 2 3-42 2-03 3-16 19-5 33-35 19-76 30-82 2-5 4-28 2-54 3-95 20 34-20 20-26 31-61 3 5-13 3-04 4-74 20-5 35-06 20-77 32-40 3-5 5-99 3-55 5-53 21 35-91 21-27 33-19 4 6-84 4-05 6-32 21-5 36-77 21-78 33-98 4-5 7-70 4-56 7-11 22 37-62 22-29 34-77 5 8-55 5-06 7-90 22-5 38-48 22-80 35-56 5-5 9-41 6-57 8-69 23 39-33 23-30 36-35 6 10-26 6-08 9-48 23-5 40-19 23-81 37-14 6-5 11-12 . 6-59 10-27 24 41-04 24-31 37-93 7 11-97 7-09 11-06 24-5 41-90 24-82 38-72 7-5 12-83 7-60 11-85 25 42-75 25-32 39-51 8 13-68 8-10 12-64 25-5 43-61 25-83 40-30 8-5 14-54 8-61 13-43 26 44-46 26-34 41-09 9 15-39 9-12 14-22 26-5 45-32 26-85 41-88 9-5 16-25 9-63 15-01 27 46-17 27-35 42-67 10 17-10 10-13 15-81 27-5 47-03 27-86 43-46 10-5 17-96 10-64 16-60 28 47-88 28-36 44-25 11 18-81 U-14 17-39 28-5 48-74 28-37 45 04 11 '5 19-67 11-65 18-18 29 49-59 29-38 45-83 12 20-52 12-17 18-97 29-5 50-45 29-89 46-62 12-5 21-38 12-68 19-76 30 51-30 30-39 47-42 13 22-23 13-17 20-55 30-5 52-16 30-90 48-21 13-5 23-09 13-68 21-34 31 53-01 31-41 49-00 14 23-94 14-18 22-13 31-5 53-87 31-91 49-79 14-5 24-80 14-69 22-92 32 54-72 32-42 50-88 15 25-65 15-19 23-71 32-5 55-58 32-92 51-37 15-5 26-51 15-70 24-50 33 56-43 33-43 52-16 16 27-36 16-21 25-29 33-5 57-29 33-94 62-95 16-5 28-22 16-73 26-08 34 58-14 34-44 53-74 17 29-07 17-22 26-87 34-5 59-00 34-95 54-53 17-5 29-93 17-73 27-66 35 59-85 35-46 55-32 SODA ASH MANUFACTURE 181 FRENCH, QEBMAN, AND ENGLISH COMMEBCIAL ALKALI- METBIOAL DEQUEES— Oantimied. Real German New- castle Real German New- castle Soda. degrees. French Soda. degrees. French NaaO. NaaCOs. degrees. degrees. NaaO. NaaCOa. degrees. degrees. 35-5 60-71 35-96 56-11 53 90-63 53-70 83-77 36 61-56 36-47 56-90 53-5 91-49 54-20 84-56 36-5 62-42 36-98 57-69 54 92-34 54-71 85-36 37 63-27 37-48 58-48 54-5 93-20 55-22 86-14 37-5 64-13 37-98 59-27 55 94-05 55-72 86-93 38 64-98 38-50 60-06 65-5 94-91 56-23 87-72 38-5 65-84 39-00 60-85 56 95-76 56-74 88-52 39 66-69 39-51 61-64 56-5 96-62 57-24 89-31 39-5 67-55 40-02 62-43 57 97-48 57-75 90-10 40 68-40 40-62 63-22 57-5 98-33 58-26 90-89 40-5 69-26 41-03 64-01 58 99-18 58-76 91-68 41 70-11 41-54 64-81 59-5 100-04 59-72 92-47 41-5 70-97 42-04 65-60 59 100-89 59-77 93-26 42 71-82 42-55 66-39 69-5 101-75 60-28 94-06 42-5 72-68 43-06 67-18 60 102-60 60-79 94-84 43 73-53 43-57 67-97 60-5 103-46 61-30 95-63 43-5 74-39 44-07 68-76 61 104-31 61-80 96-42 44 75-24 44-58 69-55 61-5 105-17 62-31 97-21 44-5 76-10 45-08 70-34 62 106-02 62-82 98-00 45 76-95 45-69 71-13 62-5 106-88 63-32 98-79 45-5 77-81 46-10 71-92 63 107-73 63-83 99-58 46 78-66 46-60 72-71 63-5 108-59 64-33 100-37 46-5 79-52 47-11 73-50 64 109-44 64-84 101-16 47 80-37 47-62 74-29 64-5 110-30 65-35 101-95 47-5 81-23 48-12 75-08 65 111-15 65-85 102-74 48 82-08 48-63 75-87 65-5 112-01 66-36 103-53 48-5 82-94 49-14 76-66 66 112-86 66-87 104-32 49 83-79 49-64 77-45 66-5 113-72 67-37 105-11 49-5 84-65 50-15 78-24 67 114-57 67-88 105-90 50 85-50 50-66 79-03 67-5 115-43 68-39 106-69 50-5 86-36 51-16 79-82 68 116-28 68-89 107-48 51 87-21 51-67 80-61 68-5 117-14 69-40 108-27 51-5 88-07 52-18 81-40 69 117-99 69-91 109-06 52 88-92 52-68 82-19 69-5 118-85 70-41 109-85 52-5 89-78 53-19 82-98 70 119-70 70-92 110-64 182 THE TECHNICAL CHEMISTS' HANDBOOK FRENCH, GERMAN, AND ENGLISH COMMEROIAIj ALKALI- METRICAL DEGREES— OoMimwed Real German New- castle degrees. Eeal German New- castle degrees. Soda. NajO. degrees. NagCOs. French degrees. Soda. NaaO, degrees. NagCOs. French degrees. 70-5 120-56 71-43 111-43 75-5 129-11 76-49 119-34 71 121-41 71-93 112-23 76 129-96 77-00 120-13 71-5 122-27 72-44 113-02 76-5 130-82 77-51 120-92 72 123-12 72-95 113-81 77 131 -S7 78-01 121-71 72-5 123-98 73-45 114-60 77-5 132-53 78-52 122-50 73 124-83 73-96 115-39 73-5 125-69 74-47 116-18 74 126-54 74-97 116-97 74-5 127-40 75-48 117-76 75 128-25 75-99 118-55 I. — Sulphur Recovery (Chance Process). 1. JSstimation of Stdphur as Svlphide in Vat Waste. — The apparatus consists of a small flask fitted with a stopcock funnel and outlet tube connected with two Mohr's potash bulbs, the first one being empty, the second containing a strong solution of caustic potash. (In lieu of Mohr's bulbs a tube of the shape shown in Fig. 8, p. 119, can be employed with great advantage.) It is preferable to connect the last potash bulb to an aspirator or Bunsen pump, to produce a slight vacuum. About 2 g. of vat waste is put into the flask, and a sufficient quantity of water is added. Then hydrochloric acid, diluted with its volume of water, is run in from the funnel gradually. After the decomposition has ceased, the solution is boiled, until the whole of the gases are displaced by steam, most of the steam condensing in the first empty potash bulbs. When enough steam has been produced to bring the first bulb of the second set, filled with potash solu- tion, up to boiling, the tap of the funnel is opened, and the apparatus allowed to cool down. The potash solution is then transferred to a J or ^ litre flask, made up to the mark, an aliquot part taken, diluted with a large quantity of previously boiled water (free from air), neutralised with acetic acid, and titrated with decinormal iodine, each c.c. of which indicates 0-001604 g. S. 2. Svlphur as Svlphide in Carbonated Mvd. — About 6 g. is taken for analysis ; otnerwise the test is conducted just like the preceding one. 3. Svlphide-svlphw+ Carbonic Add in Vat Waste. — This test SODA ASH MANUFACTURE 183 (■which is only exceptionally made) is carried out in a small flask, fitted with stopcock funnel, connected with a U-tube containing sodium sulphate to absorb any traces of HCl passing over, and a sufficient number of chloride of calcium tubes to thorouj;hly dry the gases. To the last of these are connected two wei^rhed potash bulbs containing a strong solution pi caustic potash, followed by weighed CaClj tubes. The whole apparatus being connected, 2 g. of vat waste is put into the flask, and some water added. A current of nitrogen is then passed through the apparatus to dis- place the air. [The nitrogen for this purpose is conveniently made by passing lime-kiln gases through a solution of caustic soda, then through a red-hot tube containing bright copper clippings to absorb any oxygen, and flnally through solutions of caustic potash and barium hydroxide.] The vat waste is then decomposed by hydrochloric acid, and the contents of the flask are boiled. After- wards a current of nitrogen is passed through the apparatus for a considerable time to displace the H2S and CO2 in the flask and drying tubes. The potash bulbs and the last drying tubes are reweighed, the increase showing the amount of H2S+CO2 in the vat waste employed. The potash solution is then transferred to a measuring flask, and the H2S estimated as described in 1, Deduct- ing the amount from the increase of weight of the absorbing apparatus, we find the amount of CO2 present. 4. Sulphur as Siilphide in Solutions of Calcium or Sodium Sulphydrates a/nd Sulphides. — 10 c.c. is diluted to 250, and of this liquid a convenient portion is taken out, largely diluted with air-free water, acidulated with acetic acid, and titrated with iodine, as in test 1. If thiosulphates are present, they are esti- mated as in 5, and deducted. If polysulphides are present, the sulphur which would be precipitated by an acid is not estimated by this method, but only that which would be liberated as H2S by an acid. 5. Soda, Lime, and Thiosulphate in Sulphur Liqvars. — In one sample of the liquor, say 5 c.c, estimate the total alkalinity, i.e. NasO-l-CaO, by standard hydrochloric acid and methyl orange. Take another sample, say 50 c.c, pass pure CO2 in till lead paper shows the absence of all sulphides, boil to decompose calcium bicarbonate, dilute with water to 500 c.c, aUow the precipitate to settle, take 50 c.c. of the clear liquor and titrate again, the alkalinity this time being due to Na20 only. CaO is found from the difference between the two titrations. Another sample of the' carbonated liquor is titrated with deci- normal iodine for thiosulphate. Each c.c. of iodine solution indicates 0"006414 g. S. as thiosulphate. 6. Lirhe-kiln Oases. — CO2 is estimated by an Orsat apparatus, or a Honigmann burette, or any other similar apparatus. When using an Orsat apparatus, the test for oxygen can be made as on p. 95. 184 THE TECHNICAL CHEMISTS' HANDBOOK 7. Gas from Gas-holder. (a) Hyd/rogen Sidphide + Carbon Dioxide are estimated by an Orsat apparatus or a Honigmann burette, etc. (b) Hydrogen Sidphide only. — A wide-mouthed bottle of known capacity, holding about 500 c.c, is fitted with a rubber cork and two tubes, one nearly reaching to the bottom, the other ending just below the cork, both of them with stopcocks outside. Gas is passed through for some time, till it has entirely displaced- the air in the bottle. Then 20 or 25 c.c. of standard potash solution is run in from a pipette, through one of the stop- cocks, the bottle is well shaken until the whole of the HjS and CO2 are absorbed, the contents of the bottle are poured into a measuring flask, the bottle is rinsed out completely, and the total liquid made up to the mark. An aliquot portion is taken out, largely diluted with pre- viously boiled water, acidified with acetic acid, and the HjS estimated by iodine. In this case a solution of iodine is employed containing 11'463 g. I per litre, each c.c. of which indicates 1 c.c. of gaseous HjS at 0° C. and 760 mm. pressure. For somewhat exact estimations, the temperature, pressure, and vapour tension have to be taken into account ; but it is unnecessary to observe the thermometer and barometer, and to make any complicated calculations, if a Lunge's gas- volumeter be used (p. 139). In this case the level-tube, C, of the instrument is placed so that the mercury stands at the same height in C as in the reduction tube B ; the height of mercury in the latter is read off, which gives the volume occupied by 100 c.c. of dry air of 0° and 760 mm. under the prevailing atmospheric conditions ; the number of c.c. of iodine solution, multiplied by 100, is divided by this figure, and thus the correction of the normal volume effected. 8. Eodt Gases from the Glaus Kilns. — These contain SO2 and HjS. Both these gases, on being passed through iodine solution, produce 2HI for each atom of S ; but whilst HjS does not further increase the acidity of the solution, SO.2 produces its equivalent of H2SO4. Hence SO2 and H2S are measured together by the amount of iodine converted into HI, and SO2 by the acidity present after the HI has been saturated with caustic soda. Since the current of gases carries away some iodine from the decinormal solution, the gases must be passed through caustic soda, or, better, through sodium thiosulphate, to intercept this iodine. The manipulation is hence as follows : Aspirate one or more litres of the gases through 50 c.c. of decinormal iodine solution, contained in a bulb apparatus (Fig. 8, p. 119), or other efficient absorbing-tubes, followed by another apparatus contain- ing 50 c.c. of decinormal thiosulphate solution. Empty the con- tents of both apparatus into a beaker, and titrate with deci- normal iodine and starch solution, till a blue colour appears. The number o# c.c. of iodine solution used, if multiplied by 0"001604 g. MANUFACTURE OF SODA 185 indicates the total sulphur present as SO2 and HjS. Now add a drop of thiosulphate solution to discharge the blue colour, then a drop of methyl orange, and decinormal caustic soda from a burette, till the pink colour of the liquid is discharged. The number of c,c. of caustic soda used, less those of iodine used in the preceding test, multiplied by 0'001604, indicates the sulphur present as SO2. VI. MANUFACTURE OF SODA BY THE AMMONIA PROCESS. A. — RaAV Materials. 1. Rock Salt, compare p. 146. 2. Brine. — The following determinations are made : — (a) Specific Gravity, by the hydrometer. (b) Chlorine, expressed as NaCl. Dilute 10 c.c. to 1 litre, and titrate 10 c.c. of the diluted solution as on p. 146. (c) Sulphates. — Dilute 50 c.c. brine to 150 or 200 cc, add a little hydrochloric acid, and precipitate with barium chloride as on p. 109. . (d) Ferric Oxide and Alumina. — To 500 c.c. brine add a little nitric acid, heat to 80°, precipitate by an excess of ammonia, digest for half an hour at 80°, filter, and wash well. As a check, redissolve the precipitate in hydrochloric acid and reprecipitate it by ammonia. In the filtrate lime and magnesia may be estimated as on p. 147. (e) Bicarhondtes of Iron, Lime, and Magnesia. — Destroy the bicarlDonates as such by prolonged boiling of 500 c.c, replace the water driven off, filter the precipitate formed, wash it, dissolve it in hydrochloric acid, and in the solution estimate the iron by precipitation with NH3, and lime and magnesia in the ordinary way. 3. Concentrated Gas Liquor or Sulphate of Ammonia, cf. Chapter XL, pp. 217 and 219. 4. Limestone, cf. p. 157. 5. Quicklime, cf. p. 158. 6. Coals or Coke, cf . p. 93. B. — Tests made during the Process of Manufacture. 1. Ammoniacal Brine from the receivers. (a) Sodium Chloride. — Acidulate with nitric acid and estimate the NaCl by AgNOg gravimetricaUy, or volumetrically in the neutral or faintly alkaline solution as on p. 146. 186 THE TECHNICAL CHEMISTS' HANDBOOK (b) Ammonia, free amd combined. — Dilute 10 c.c. to 100 c.c. and boil in a distilling flask until all tie free ammonia^ and ammonium carbonate has been expelled ; absorb this in a measured volume of normal sulphuric acid, and titrate back. To the solution remaining in the flask add caustic soda solution, distil again, and absorb this " combined " ammonia also in sulphuric acid. Of. Chapter XI., p. 217. 2. Carbonators. — Free and combined NH3 are estimated as in No. 1 (b). 3. Mother Liqitxyr. — Estimate : — (a) NH3, free and combined, as above. (b) Undecomposed NaCl, by evaporating 10 c.c. in a platinum dish, heating until aU NH4CI is expelled, and weighing. 4. Crude Bicarbonate. — Estimate : — (a) The Alhalimetrical Degree, as on p. 167. fb) CO2 as on p. 171. (c) Moisture, by igniting and allowing for the CO2 present as bicarbonate and found in (b). 5. Distillation of Anvmonia : — (a) NH3, free and combined, in the mother liquor, as in No. 1(b). (b) Milk of lime, as on p. 158. (c) Excess of lime in the stills. Boil 100 c.c. until all NH3 has been expelled, add a little ammonium sulphate, and boil again. The NH3 now set free, which corresponds to the excess of lime, is absorbed in standard sulphuric acid and titrated. 6. Lime-hiln Gases. — Estimate the CO2 as on p. 95. 0. — Commercial Products. 1. Soda Ash, as on p. 178. 2. Gom/mercial Bicarbonate is tested like the crude, No. 1, or very accurately by heating in an air-bath to 270° and receiving the gas in a Lunge's gas-volumeter, p. 139 (compare Lunge, Z. angew. Chem., 1897, p. 522). VII. CAUSTIC SODA. A. — Caustic Liquor. (a) Test for available alkali and sodium carbonate (as described p. 167). An exact estimation of CO2, which is rarely necessary in this case, could be made by expelling it with dilute sulphuric acid, and absorbing it in soda-lime, or, preferably, by Lunge and Eittener's method, p. 171. CAUSTIC SODA 187 (5) SPECIFIC GRAVITIES OP SOIiUTIONS OP SODIUM HYDROXIDE AT 15° C. 1 cb.m. contains kg. Specific Gravity. Degrees Twaddell. Degrees Bauin6. Per cent. NaaO. Per cent. NaOH. NaaO. NaOH. 1-000 0-00 1-005 1 0-7 0-33 0-43 3-31 4-32 1-010 2 1-4 0-67 0-86 6-77 8-69 1-015 3 2-1 0-99 1-28 10-05 12-99 1-020 4 2-7 1-31 1-69 13-36 17-24 1-025 5 3-4 1-65 2-13 16-91 21-83 1-030 6 4-1 2-02 2-60 20-81 26-78 1-035 7 4-7 2-37 3-06 24-53 31-67 1-040 8 5-4 2-71 3-50 28-18 36-40 1-045 9 6-0 3-02 3-90 31-56 40-76 1-060 10 6-7 3-36 4-34 35-28 45-67 1-055 11 ,7-4 3-69 4-76 38-93 50-22 1-060 12 8-0 4-03 5-20 42-72 56-12 1-065 13 8-7 4-39 5-67 46-75 60-39 1-070 14 9-4 4-75 6-13 50-83 66-59 1-075 15 10-0 5-10 6-58 54-83 70-74 1-080 16 10-6 5-46 7-05 58-97 76-14 1-085 17 11-2 5-81 7-50 63-04 81-38 1-090 18 11-9 6-16 7-95 67-14 86-66 1-095 19 12-4 6-60 8-39 71-18 91-87 1-100 20 13-0 6-81 8-78 74-91 96-58 1-105 21 13-6 7-15 9-23 79-01 101-99 1-110 22 14-2 7-50 9-67 83-25 107-34 1-115 23 H-9 7-84 10-12 87-42 112-84 1-120 24 15-4 8-18 10-56 91-62 118-27 1-125 25 16-0 8-57 11-06 96-41 124-43 1-130 26 16-5 8-95 11-65 101-14 130-52 1-135 27 17-0 9-32 12-02 105-78 136-43 1-140 28 17-7 9-68 12-49 110-35 142-39 1-145 29 18-3 10-03 12-94 114-84 148-16 1-150 30 18-8 10-34 13-34 118-91 153-41 1-155 31 19-3 10-67 13-76 123-24 158-93 1-160 32 19-8 11-00 14-19 127-60 164-60 1-165 33 20-3 11-33 14-62 131-99 170-32 1-170 34 20-9 11-67 15-06 136-54 176-20 1-175 35 21-4 12-04 15-53 141-47 182-48 1-180 36 22-0 12-40 16-00 146-32 188-80 1-185 37 22-5 12-75 16-45 151-09 194-93 1-190 38 23-0 13-11 16-91 156-01 201-23 1-195 39 23-5 13-46 17-36 160-85 207-45 1-200 40 24-0 13-80 17-81 166-60 213-72 1-205 41 24-5 14-15 18-26 170-51 220-03 188 THE TECHNICAL CHEMISTS' HANDBOOK (6) SPECIFIC GRAVITIBS OP SOLUTIONS OP SODIUM HYDROXIDE AT 15° C.—Oontinued. 1 cb.m. contains kg. Specific Gravity. Degrees TwaddeU. Degrees liaum^. Per cent. NaaO. Per cent. NaOH. NajO. NaOH. 1-210 42 25-0 14-50 18-71 175-45 226-39 1-215 43 25-5 14-87 19-18 180-67 233-04 1-220 44 26-0 15-23 19-65 185-81 239-73 1-225 45 26-4 15-59 20-12 190-98 246-47 1-230 46 26-9 15-97 20-60 196-43 253-38 1-235 47 27-4 16-30 21-03 201-31 259-72 1-240 48 27-9 16-64 21-47 206-34 266-23 1-245 49 28-4 16-97 21-90 211-28 272-66 1-250 50 28-8 17-31 22-33 216-38 279-13 1-255 51 29-3 17-65 22-77 221-51 285-76 1-260 52 29-7 18-01 23-23 226-93 292-70 1-265 53 30-2 18-35 23-68 232-13 299-55 1-270 54 30-6 18-70 24-13 237-62 306-45 1-275 55 31-1 19-05 24-58 242-89 313-40 1-280 56 31-5 19-41 25-04 248-45 320-51 1-285 57 32-0 19-77 25-50 254-04 327-68 1-290 58 32-4 20-12 25-96 259-55 334-88 1-295 59 32-8 20-47 26-41 265-09 342-01 1-300 60 33-3 20-81 26-85 270-53 349-05 1-305 61 33-7 21-20 27-35 276-66 356-92 1-310 62 34-2 21-59 27-85 282-83 364-83 1-315 63 34-6 21-97 28-34 288-91 372-67 1-320 64 35-0 22-35 28-83 295-02 380-56 1-325 65 35-4 22-73 29-32 301-17 388-40 1-330 66 35-8 23-10 29-80 307-23 396-34 1-335 67 36-2 23-47 30-28 313-32 404-24 1-340 68 36-6 23-83 30-74 319-32 411-92 1-345 69 37-0 24-18 31-20 325-22 419-64 1-350 70 37-4 24-61 31-75 332-24 428-63 1-355 71 37-8 25-02 32-28 339-02 437-39 1-360 72 38-2 25-42 32-79 345-71 445-94 1-365 73 38-6 25-78 33-26 351-90 454-00 1-370 74 39-0 26-14 33-73 358-12 462-10 1-375 75 39-4 26-62 34-22 364-65 470-53 1-380 76 39-8 26-90 34-71 371-22 479-00 1-385 77 40-1 27-28 35-20 377-83 487-52 1-390 78 40-5 27-66 35-68 384-47 495-95 1'395 79 40-8 28-02 36-15 390-88 504-29 1-400 80 41-2 28-42 36-67 397-88 513-38 1-405 81 41-6 28-81 37-17 404-78 522-24 1-410 82 42-0 29-18 37-65 411-44 530-87 1-415 83 42-3 29-58 38-16 418-56 539-96 CAUSTIC SODA 189 (6) SPECIFIC GRAVITIES OF SOLUTIONS OF SODIUM HYDROXIDE AT 15° O.— Continued. 1 cb.m. contains kg. Speciflc Gravity. Degrees TwaddeU. Degrees Baum6. Per cent. NaaO. Per cent. NaOH. NaaO, NaOH. 1-420 84 42-7 29-97 38-67 426-57 549-11 1-425 85 43-1 30-36 39-17 432-63 558-17 1-430 86 43-4 30-75 39-67 439-72 567-28 1-435 87 43-8 31-14 40-18 446-86 576-68 1-440 88 44-1 31-53 40-68 454-03 585-79 1-445 89 44-4 31-93 41-20 461-39 695-34 1-450 90 44-8 32-32 41-70 468-64 604-65 1-455 91 45-1 32-72 42-22 476-07 614-30 1-460 92 45-4 33-14 42-75 483-84 624-15 1-465 93 45-8 33-54 43-27 491-36 633-91 1-470 94 46-1 33-95 43-80 499-07 643 86 1-475 95 46-4 34-36 44-33 506-81 663-87 1-480 96 46-8 34-76 44-85 514-45 663-78 1-485 97 47-1 35-17 45-37 522-27 673-74 1-490 98 47-4 35-57 45-89 S29-99 683-76 1-495 99 47-8 35-98 46-42 637-90 693-98 1-600 100 48-1 36-38 46-94 545-70 704-10 1-505 101 48-4 36-79 47-47 563-69 714-42 1-510 102 48-7 37-20 48-00 561-72 724-80 1-515 103 49-0 37-61 48-53 569-79 735-23 1-520 104 49-4 38-02 49-05 577-90 745-56 1-525 105 49-7 38-42 49-58 685-91 756-10 1-530 106 50-0 38-83 50-10 594-10 766-53 190 THE TECHNICAL CHEMISTS' HANDBOOK (c) INFLUBNOB OP TEMPERATURE ON THE SPBCIPIO 0"O. 16°. 20°. 1-360 1-357 1-350 1-347 1-340 1-338 1-330 1-328 1-320 1-318 1-310 1-308 1-300 1-297 1-290 1-287 1-280 1-277 1-270 1-267 1-260 1-267 1-250 1-247 1-240 1-237 1-230 1-227 1-220 1-217 1-210 1-207 1-200 1-1B7 1-190 1-187 1-180 1-177 1-170 1-167 1-160 1-157 1-150 1-148 1-140 1-138 1-130 1-128 1-120 1-118 1-110 1-108 1-100 1-098 1-090 1-088 1-080 1-078 1-070 1-068 1-060 1-068 1-050 1-048 1-040 1-038 1-030 1-028 1-020 1-018 1-010 1-008 1-367 1-364 1-367 1-354 1-347 1-344 1-338 1-336 1-328 1-325 1-318 1-315 1-308 1-305 1-298 1-295 1-288 1-285 1-278 1-275 1-268 1-265 1-257 1-256 1-247 1-246 1-237 1-235 1-227 1-226 1-217 1-215 1-207 1-205 1-197 1-195 1-187 1-185 1-176 1-174 1-166 1-164 1-156 1-164 1-146 1-144 1-136 1-134 1-126 1-124 1-115 1-113 1-105 1-108 1-094 1-093 1-084 1-083 1-074 1-078 1-064 1-063 1-054 1-068 1-044 1-043 1-034 1-033 1-024 1-023 1-014 1013 1-362 1-352 1-342 1-332 1-322 1-813 1-303 1-293 1-283 1-273 1-263 1-252 1-242 1-232 1-222 1-212 1-202 1-192 1-182 1-172 1-162 1-162 1-142 1-132 1-122 1-112 1-102 1-091 1-081 1-071 1-061 1-061 1-041 1-031 1-021 1-355 1-346 1-335 1-325 1-316 1-306 1-294 1-284 1-274 1-265 1-255 1-245 1-235 1-224 1-214 1-204 1-195 1-186 1-175 1-165 1-155 1-146 1-136 1-126 1-116 1-106 1-096 1-087 1-077 1-067 1-057 1-047 1-037 1-027 1-017 1-007 1-363 1-343 1-333 1-323 1-318 1-303 1-292 1-282 1-272 1-262 1-^2 1-242 1-232 1-222 1-212 1-203 1-193 1-183 1-173 1-163 1-153 1-144 1-134 1-124 1-114 1-104 1-095 1-086 1-076 1-066 1-066 1-046 1-036 1-026 1-016 1-006 1-350 1-340 1-330 1-320 1-310 1-300 1-289 1-279 1-269 1-260 1-250 1-240 1-230 1-220 1-210 1-200 1-190 1-180 1-170 1-161 1-151 1-142 1-132 1-122 1-112 1-102 1-093 1-084 1-074 1-064 1-054 1-044 1-034 1-024 1-014 1-348 1-337 1-327 1-317 1-307 1-297 1-287 1-277 1-267 1-258 1-248 1-238 1-228 1-218 1-208 1-198 1-188 1-178 1-168 1-158 1-148 1-140 1-130 1-120 1-110 1-100 1-092 1-082 1-072 1-062 1-052 1-042 1-032 1-022 1-012 1-004 1-002 I 1-345 1-336 1-325 1-316 1-305 1-294 1-284 1-274 1-264 1-265 1-245 1-235 1-226 1-215 1-206 1-196 1-186 1-176 1-166 1-156 1-146 1-137 1-127 1-118 1-108 1-099 1-090 1-080 1-070 1-060 1-060 1-040 1-030 1-020 1-010 1-000 CAUSTIC SODA GRAVITIES OF SOLUTIONS OP CAUSTIC SODA. 191 65°. 60'. 65°. 70°. 75°. 80". 85°. 90°. 96°. 100°. 1-339 1-336 1-338 1-331 1-828 1-326 1-823 1-821 1-318 1-316 l-SSO 1-327 1-324 1-822 1-319 1-316 1-S14 1-311 . 1-808 1-806 1-320 1-817 1-314 1-312 1-309 1-306 1-804 1-301 1-298 1-296 1-310 1-307 1-804 1-302 1-299 1-296 1-294 1-291 1-288 1-286 1-800 1-297 1-294 1-292 1-289 1-286 1-283 1-280 1-277 1-274 1-289 1-286 1-284 1-281 1-278 1-276 1-272 1-269 1-266 1-263 1-279 1-276 1-274 1-271 1-268 1-266 1-262 1-259 1-266 1-268 1-269 1-266 1-264 1-261 1-268 1-256 1-262 1-249 1-245 1-242 1-259 1-256 1-264 1-261 1-248 1-245 1-242 1-239 1-236 1-282 1-250 1-247 1-246 1-242 1-239 1-286 1-238 1-281 1-228 1-226 1-240 1-287 1-235 1-232 1-229 1-226 1-223 1-221 1-218 1-216 1-231 1-228 1-226 1-223 1-220 1-218 1-216 1-213 1-209 1-207 1-221 1-218 1-216 1-218 1-210 1-208 1-205 1-208 1-200 1-197 1-210 1-208 1-206 1-202 1-200 1-198 1-196 1-192 1-190 1-187 1-200 1-198 1-196 1-192 1-190 1-188 1-185 1-182 1-180 1-177 1-191 1-189 1-186 1-184 1-181 1-179 1-176 1-178 1-171 1-168 1-182 1-180 1-177 1-175 1-172 1-169 1-166 1-163 1-161 1-158 1-1?2 1-169 1-166 1-164 1-161 1-158 1-156 1-168 1-160 1-147 1-162 1-169 1-166 1-163 1-151 1-148 1-146 1-143 1-140 1-137 1-152 1-149 1-146 1-148 1-140 1-138 1-186 1-132 1-130 1-127 1-142 1-139 1-136 1-lSS 1-130 1-128 1-126 1-122 1-120 1-117 1-132 1-130 1-127 1-124 1-121 1-118 1-116 1-113 1-110 1-107 1-122 1-120 1-117 1-114 1-111 1-108 1-ioa 1-108 1-100 1-097 1-llS 1-110 1-107 1-104 1-101 1-099 1-006 1-093 1-090 1-087 1-103 1-100 1-097 1-094 1-092 1-089 1-086 1-088 1-080 1-077 1-094 1-091 1-089 1-086 1-088 1-080 1-077 1-074 1-071 1-068 •1-084 1-082 1-079 1-076 1-073 1-070 1-067 1-064 1-061 1-058 1-075 1-073 1-070 1-067 1-064 1-061 1-068 1-066 1-062 1-048 1-066 1-063 1-060 1-067 1-054 1-061 1-048 1-046 1-043 1-040 1-066 1-053 1-050 1-047 1-044 1-042 1-089 1-036 1-033 1-030 1-046 1-043 1-040 1-037 1-084 1-082 1-029 1-026 1-028 1-020 1-036 1-033 1-080 1-027 1-024 1-021 1-019 1-016 1-018 1-010 1-026 1-023 1-020 1-017 1-014 1-011 1-009 1-006 1-003 1-000 1-016 1-013 1-010 1-007 1-004 1-001 0-999 0-996 0-998 0-990 1-006 1-003 1-000 0-997 0-994 0-991 0-989 0-986 0-983 0-980 0-906 0-99S 0-990 0-087 0-984 0-981 0-979 0-976 0-973 0-970 192 THE TECHNICAL CHEMISTS' HANDBOOK B. — Lime Mud. (a) Sodium as Carbonate and Hydroxide. — Evaporate to dry- ness with addition of ainmonium carbonate (in order to decompose the insoluble sodium compounds), repeat this, digest with hot water, filter, wash, and test the filtrate for alkali. The soda may- have been originally present as NaOH or as Na^COj. It is expressed iu terms of NajO (O'OSIOO g. per cubic centimetre of normal acid). (b) Caustic Lime. — Titrate as described (p. 158) with normal hydrochloric acid and phenolphthalein. This indicates NaOH as well, for which half of the amount found in test (a) may be assumed without any serious error. (c) Calcium Carbonate. — Titrate with normal hydrochloric acid and methyl orange, deduct from the cubic centimetres required those required in tests (a) and (b). 0. — Fished Salts. Dissolve 50 g. in 1 litre of water, and take 50 c.c. of the solu- tion for every test. (a) Available Alkali is tested for with normal hydrochloric acid. (b) Sodium Chloride. — Neutralise with nitric acid, preferably running normal acid out of a burette, and proceed in other respects as described on p. 146. (c) Sodium Sulphate. — Add a slight excess of hydrochloric acid, precipitate with barium chloride, and weigh the BaS04 (p. 109). (d) Sodium Sulphite, Thiosvlphate, etc. — Add an excess of bleaching-powder solution, then hydrochloric acid, till the reaction is acid, and a smeU of chlorine is produced (p. 168) ; precipitate with BaCl2, weigh the BaSOi, and deduct the amount found in test (c). The remainder is calculated as " NajSOj from oxidisable sulphur compounds." D. — Caustic Bottoms. Dissolve 10 g. in water, and filter. The washed residue is dried and ignited, and yields": — (a) Insoluble Matter. — If necessary, the contained iron is estimated by dissolving in concentrated hydrochloric acid, reduc- ing with zinc, adding manganous sulphate, and titrating with permanganate as on p. 112. ELECTEOLYTIC ALKALI LIQUORS 193 (b) Available Alkali is estimated in the aqueous solutions by- normal hydrochloric acid, using litmus or lacmoid as indicator. (Methyl orange is not available in this case, owing to the presence of alumina.) (c) Sodium Carbonate is estimated as in commercial soda ash (p. 178). S. — Commercial Caustic Soda. The sample must be very carefully taken. (Cf. Appendix.) The single pieces must be freed from the outer crust by scraping it off, before weighing. Dissolve 50 g. of the prepared sample in 1 litre of water, and take aliquot portions for each of the following tests with a pipette. (a) Available Alkali is tested in at least 20 c.c. (equal to 1 g.) by normal HCl. If the caustic soda contains more than traces of alumina, methyl orange cannot be used as indicator, but litmus or lacmoid should be employed. In the case of strong caustic this is unnecessary. (b) Sodiwn Carbonate is estimated by expelling the CO2 with dilute sulphuric acid, and absorbing it in soda-lime (the pumice saturated with cupric sulphate is left out here), or by Lunge and Rittener's process, p. 171. The quantity of CO2 being so small, any estimation by difference yields unsatisfactory results. Very approximate results can, however, be obtained by titrating first with phenolphthalein till the pink colour is discharged (when all Na2C03 will have been changed into NaHCOj), noting the amount of standard acid used, adding methyl orange and more standard acid till the pink colour appears. The acid used in the second test X 2 indicates Na2COs. (c) The Table for comparing English, French, and German Degrees is given on pp. 180 to 182. Vni. ELECTROLYTIC ALKALI LIQUORS. These are analysed just like bleach liquor, p. 164. 1. Hypochlorites are titrated as on p. 159. 2. Free Hypochlorous Acid. — Estimate the bleaching chlorine as in No. 1, then chloride, chlorate, and other acids on the one hand, and all bases on the other : the acidity in excess represents free HOCl. 3. Chlorate may be estimated as on p. 164, but since there is but little chlorate in presence of much hypochlorite, it is prefer- N 194 THE TECHNICAL CHEMISTS' HANDBOOK able to use the direct method of Fresenius, as follows : — To the solution add an excess of neutral lead acetate solution ; this pro- duces a precipitate which gradually turns brown, and which contains a quantity of Pb02 corresponding to the chlorate. Allow to stand for eight or ten hours, until there is no more smell of chlorine, filter, wash, evaporate the filtrate to a small volume, precipitate lead and lime by means of a little sodium carbonate, and estimate the chlorate in the filtrate according to p. 164. In mixtures of chlorate and hypochlorite, containing large quantities of the latter, Ditz and Knopfehnacher estimate the chlorate iodometrically, by decomposing it at the ordinary temperature with concentrated hydrochloric acid and potassium bromide. Put the substance, together with a sufficient excess of KBr, into a small flask provided with a hollow glass stopper with dropjjing funnel and lateral absorbing vessel for the retention of bromine vapours. The latter is charged with 10 c.c. of a 5 per cent, solution of KI. Pour 50 c.c. concentrated hydrochloric acid through the dropping funnel into the flask, allow it to act for an hour, pour in 300 c.c. water, then 20 c.c. of the solution of KI, shake well, transfer the contents of the absorbing vessel to the flask, and titrate the iodine which has been set free by thiosul- phate. The quantity of chlorate + hypochlorite is thus ascertained. If there is very much of the latter present, it should be removed beforehand. 4. Chloride. — Employ the solution from No. 1, in which all hypochlorite has been converted into chloride, with formation of sodium arsenate, which is an excellent indicator for the titration of the total chlorides by silver nitrate, p. 148, making no deduction for any excess of silver nitrate required to produce the colour. From the quantity of chloride thus found, deduct that which corresponds to the hypochlorite. 5. Carbon Dioxide. — Destroy the hypochlorite by boiling with liquor ammonias, free from COj, expel the CO2 by a strong acid, and estimate it as on p. 171. 6. Bases. — Convert these into sulphates, by evaporation with sulphuric acid, and estimate them in the residue by the ordinary methods. 7. Free Alkali. — Add to the solution a little of Merck's chemically pure hydrogen peroxide, which reacts as follows with the hypochlorite : — NaOCl + H2O2 = NaCl + BJO + O^. NaOH and NagCOs remain unchanged in solution, and are titrated as on p. 167. In regard to the estimation of carbon dioxide in electrolytic chlorine gas, see p. 163- NITRIC ACID MANUFACTURE 195 IX. NITRIC ACID MANUFACTURE. A. — Commercial Nitrate of Soda. According to the custom of the trade, which has held fon many years, no direct estimation of the nitrate is made in the commercial nitrate of soda exported from Chili. The rule is, to estimate moisture, sodium chloride, sodium sulphate, and in- soluble substances. The sum of these impurities is called the " refraction," and everything else is assumed to be real nitrate of soda. But as Chili saltpetre sometimes contains potassium nitrate (in which the percentage of NO3 is less than in NaNOs), errors up to 1 per cent. NaNOs or even more may be caused • by this indirect method of testing. Therefore, besides the above estimations, it ought to be insisted upon to estimate the potassium present and to calculate the results accordingly, or even better, to estimate the nitric-nitrogen directly. The sampling ought to be done very carefully, since especially the amount of moisture may vary considerably in different parts of a cargo, and the reduction of the large sample to a smaller bult ought to yield a really representative average sample. 1. Moisture. — Heat 10 g. or more of a good average sample in a small glass or porcelain dish to 130° for four or five hours, till the weight is constant. 2. Insoluble. — Dissolve 10 g. in water, filter, wash, and ignite. If there is a very appreciable quantity of organic matter present, first dry at 100° C. and weigh the filter with the precipitate before igniting it. The solution is used for the tests Nos. 4 to 6. 3. Sodium Nitrate. — In order to obtain a really representative sample, take about 20 g. of the carefully taken, large, average sample, dry this at 110°, grind it very finely, mix it thoroughly, and use it for the estimation of nitrate, etc. For the nitrate test, weigh out about 0"35 g. (that is, a quantity which will yield between 100 and 120 c.c. NO at the ordinary temperature and barometric pressure) in a narrow weighing-tube. Pour its cour tents as completely as possible into the decomposition vessel I) of the gas-volumeter. Fig. 10, p. 140, so that the substance gets as much as possible to the bottom of the beaker of D. Weigh the weighing-tube again, with the small quantity of nitrate still adhering to it, so as to ascertain the weight of nitrate taken = a, in D. The three-way tap must be closed. Now run in 0'5 c.c. water, wait until the nitrate has been entirely or nearly all dis- solved, draw the solution with any small crystals into the inside 196 THE TECHNICAL CHEMISTS' HANDBOOK of D, by lowering tte level-tube E and cautiously opening the tap, rinse the beaker with J or at most 1 c.c. water, and then allow 15 c.c. of pure concentrated sulphuric acid to enter in the same way. (It is important not to employ more than 1'5 c.c. water altogether to 15 c.c. of strong acid, for if the acid is too much diluted, a froth of basic mercuric sulphate is formed which pre- vents an exact reading of the volume. On the other hand, the addition of a little water to the strong acid prevents the solution of an appreciable quantity of NO in the liquid.) The reaction is finished by vigorous shaking of the acid solution with the mercury (as in the ordinary nitrometer, p. 137). During this period the level-tube should be roughly put into position, to avoid any considerable differences of pressure and possible leakages through the tap. When the agitating has been finished, wait half an hour for cooling. Then connect tube c of vessel D (Fig. 10, p. 140) with tube e of the measuring tube A, so that glass touches glass, as described p. 141, and transfer all the. gas to A, by raising E and lowering C, but not allowing any acid to get into A. Then shut both taps, and by adjusting the tubes A, B, C, in the manner described, p. 141, compress the gas volume to that corresponding to 0° and 760 mm. pressure. Of course it is also possible to employ, in lieu of the gas- volumeter, an ordinary nitrometer, that is, to leave out the "reduction-tube" B. In this case the volume NO is read off under the prevailing atmospheric pressure, by adjusting the level- tube accordingly ; the volume of NO is then reduced to 0° and 760 mm. by reading the thermometer and barometer, and employing the Tables 20, 1, and II., pp. 36 et seq. The reduced volume of NO we call X. Each c.c. of it corresponds to 0"0037963 g. NaNOs (com- pare the table, p. 139) ; the whole, divided by the weight of the nitrate employed a and multiplied by 100, indicates the percentage of real nitrate ; that is : — 0-37963X a ' (B'.B.—The nitrometer should be tested whether it reaUy con- tains exactly 100 c.c. to the mark 100, by inverting it, fiUmg in mercury to the mark 100, running it off, and weighing. It should weigh 1360 g. reduced to 0°, or 1355 g. at 15° 0. If there is an error, this must be allowed for in each reading.) 4. Sodium Sulphate is estimated in the solution No 2 by precipitation with BaClg and weighing the BaSO,. {Gf. pp. 109 and 148.) 5. Sodium Chloride is titrated with silver nitrate. (Gf. p. 146.) _ ^ ■" _ 6. Iodine is detected by reducing the iodic acid with zinc, heat- ing the solution with concentrated sulphuric acid, which liberates the iodine, diluting and agitating with carbon disulphide, which NITRIC ACID MANUFACTURE 197 takes up the iodine, and is thereby coloured pink. The faintest traces of iodate are found by dissolving 5 g. in 100 c.c. of boiled water, adding a little nitric acid, a few drops of a solution of potassium iodide in boiled water, and a drop of starch solution. In the presence of as little as O'Ol mg. I in 1 g. of nitre, a blue colour wOl appear. A check test must, however, be made with the potassium, iodide employed for this test, as this often contains some iodate. 7. Potassium. — Evaporate a special sample several times with strong hydrochloric acid until all the nitrate is decomposed, and estimate the K as in the analysis of potassium chloride, p. 205. Calculate it as KNO3, 100 parts of which is equivalent with 84"08 of NaNOa. 8. Perchlorate (Gilbert). — Treat 20 g. of the dried substance with 2 or 3 c.c. concentrated hydrochloric acid in a flat platinum dish ; add about 1 g. manganese dioxide, free from chlorine, dry by heating over a small flame ; bring to fusion, put on the lid and keep the dish at a red heat during one-quarter hour. Dissolve the melt in hot water and dilute the solution to 250 c.c. Take out 50 c.c. (=4 g. nitre), acidulate with nitric acid and add a 1 per cent, solution of KMnOj, until the red colour persists for a full minute. Then add ferric potassium sulphate (iron-alum), and titrate the chloride by means of silver nitrate (Volhard's method). From the CI thus found, deduct that which was originally present (No. 5), and calculate the remainder as per- chlorate. 1 part NaCl corresponds to 2'095 NaClOg. B. — Nitre-Cake. 1. Free Acid is titrated with standard alkali (p. 147). If considerable quantities of ferric oxide or alumina are present, no indicator is employed, but normal alkali is added tiU the first flakes of a precipitate indicate the end of the reaction. 2. Nitric Acid should be estimated in the gas-volumeter (p. 139), or in the nitrometer (p. 137) ; the method employed is exactly the same as described there, viz., dissolving in the beaker in very little water, and decomposing with a large excess of sulphuric acid. 3. Ferric Oxide amd Alumiiwi, (as pp. 143 and 148). [C— NiTEic Acid. 198 THE TECHNICAL CHEMISTS' HANDBOOK C. — Nitric Acid. 1. SPEOIPIC GRAVITY OF NITRIC ACID AT 15° C, COM- PARED WITH WATER OP 4° O. (IN VACUO). (Lunge and Rey.) Degrees Twad- deU. Percentage by weight. Grams per litre. NaOs. HNO3. N2O6. HNO3. 0-08 0-10 1 1 1 0-85 1-00 8 10 2 1-62 1-90 16 19 3 2-39 2-80 24 28 4 3 -17 3-70 33 38 5 3-94 4-60 40 47 6 4-71 5-50 49 57 7 5-47 6-38 57 66 8 6-22 7-26 64 75 9 6-97 8-13 73 85 10 7-71 8-99 81 94 11 8-43 9-84 89 104 12 9-15 10-68 97 113 13 9-87 11-51 105 123 14 10-57 12-33 113 132 15 11-27 13-15 121 141 16 11-96 13-95 129 151 17 12-64 14-74 137 160 18 13-31 15-33 145 169 19 13-99 16-32 . 153 179 20 14-67 17-11 161 188 21 15-34 17-89 170 198 22 16-00 18-67 177 207 23 16-67 19-45 186 217 24 17-34 20-23 195 227 25 18-00 21-00 202 236 26 18-66 21-77 211 246 27 19-32 22-54 219 256 28 19-98 23-31 228 266 29 20-64 24-08 237 276 30 21-29 24-84 245 286 31 21-94 25-60 254 296 32 22-60 26-36 262 306 33 23-25 27-12 271 316 34 23-90 27-88 279 326 NITRIC ACID MANUFACTURE 199 SPECIFIC GRAVITY OF NITRIC ACID AT 15° C, COMPARED ■WITH WATER OF 4° C. (IN VA.aUO)— Continued. Degrees Twad- dell. Percentage by weight. Grams per litre. NjOj. HNO3. NaOj. 1 HKO3. 35 24-54 28-63 288 336 36 25-18 29-38 297 347 37 25-83 30-13 306 357 38 26-47 30-88 315 367 39 27-10 31-62 324 378 40 27-74 32-36 333 388 41 28-36 33-09 342 399 42 28-99 33-82 351 409 43 29-61 34-55 360 420 44 30-24 35-28 369 430 45 30-88 36-03 378 441 46 31-53 36-78 387 452 47 32-17 37-53 397 463 48 32-82 38-29 407 475 49 33-47 39-05 417 486 50 34-13 39-82 427' 498 51 34-78 40-58 437 509 52 35-44 41-34 447 521 53 36-09 42-10 457 533 54 36-75 42-87 467 544 55 37-41 43-64 477 556 56 38-07 44-41 487 568 57 38-73 45-18 498 581 58 39-39 45-95 508 593 59 40-05 46-72 519 605 60 40-71 47-49 529 617 61 41-37 48-26 540 630 62 42-06 49-07 551 643 63 42-76 49-89 562 656 64 43-47 50-71 573 669 65 44-17 51-53 585 683 66 44-89 52-37 597 697 67 45-62 53-22 . 609 710 68 46-35 54-07 621 725 69 47-08 54-93 633 789 200 THE TECHNICAL CHEMISTS' HANDBOOK SPECIFIC GRAVITY OF NITRIC ACID AT 15° 0., COMPARED WITH WATER OF 4° C. ffN VACUO)— Continued. Twad- deU. Percentage by weigM. Grams per litre. NjOj. HNO3. N2O6. HNO3. 70 47-82 55-79 645 753 71 48-57 56-66 658 768 72 49-35 57-57 671 783 73 50-13 58-48 684 798 74 50-91 59-39 698 814 75 51-69 60-30 711 829 76 52-62 61-27 725 846 77 53-35 62-24 739 862 78 54-20 63-23 753 879 79 55-07 64-25 768 896 80 55-97 65-30 783 914 81 56-92 66-40 800 933 82 57-86 67-50 816 952 83 58-83 68-63 832 971 84 59-83 69-80 849 991 85 60-84 70-98 867 1011 86 61-86 72-17 885 1032 87 62-91 73-39 903 1053 88 64-01 74-68 921 1075 89 65-13 75-98 941 1098 90 66-24 ■77-28 961 1121 91 67-38 78-60 981 1144 92 68-56 79-98 1001 1168 93 69-79 81-42 1023 1193 94 71-06 82-90 1045 1219 95 72-39 84-45 1068- 1246 96 73-76 86-05 1092 1274 97 75-18 87-70 1116 1302 98 76-80 89-60 1144 1335 99 78-52 91-60 1174 1369 100 80-65 94-09 1210 1411 101 82-63 96-39 1244 1451 102 84-09 98-10 1270 1481 103 84-92 99-07 1287 1501 104 85-44 99-67 1299 1515 NITRIC ACID MANUFACTURE 201 2. INPLUBNCB OP TEMPERATURE ON THE SPECIPIO GRAVITY OP NITRIC ACID. O'C. 5° 10° ' 16' 20- 26" 80' 86* 40- 46° 60° 1-424 1-414 1-407 1-400 1-392 1-385 1-378 1-871 1-868 1-366 1-349 1-413 1-404 1-897 1-390 1-382 1-875 1-367 1-361 1-364 1-347 1-340 1-402 1-394 1-387 1-380 1-872 1-865 1-357 1-851 1-844 1-389 1-332 1-391 1-383 1-877 1-370 1-363 1-366 1-349 1-342 1-835 1-330 1-323 1-380 1-878 1-367 1-360 1-353 1-346 1-340 1-333 1-826 1-320 1-314 1-869 1-362 1-356 1-360 1-848 1-387 1-330 1-323 1-317 1-312 1-306 1-359 1-362 1-846 1-340 1-833 1-327 1-820 1-314 1-308 1-808 1-297 1-348 1-342 1-336 1-380 1-824 1-318 1-311 1-806 1-209 1-294 1-288 1-838 1-382 1-326 1-320 1-314 1-808 1-302 1-296 1-290 1-286 1-280 1-327 1-321 1-816 1-310 1-804 1-299 1-293 1-287 1-281 1-276 1-271 1-317 1-311 1-306 1-800 1-294 1-289 1-288 1-278 1-273 1-268 1-268 1-307 1-301 1-296 1-290 1-284 1-279 1-278 1-268 1-263 1-258 1-263 1-297 1-291 1-286 1-280 1-274 1-269 1-203 1-258 1-258 1-248 1-243 1-287 1-281 1-276 1-270 1-266 1-269 1-264 1-248 1-243 1-238 1-234 1-277 1-271 1-266 1-260 1-256 1-249 1-244 1-238 1-233 1-223 1-224 1-266 1-260 1-255 1-250 1-245 1-240 1-236 1-229 1-224 1-219 1-216 1-2B6 1-250 1-246 1-240 1-285 1-230 1-225 1-220 1-215 1-210 1-205 1-245 1-240 1-235 1-230 1-225 1-220 1-215 1-210 1-206 1-201 1-196 1-235 1-230 1-225 1-220 1-215 1-210 1-205 1-200 1-196 1-191 1-186 1-224 1-219 1-214 1-210 1-205 1-200 1-196 1-191 1-187 1-182 1-177 1-213 1-208 1-204 1-200 1-196 1-190 1-186 1-181 1-177 1-172 1-167 1-202 1-198 1-194 1-190 1-186 1-181 1-177 1-172 1-168 1-168 1-168 1-192 1-188 1-184 1-180 1-177 1-171 1-167 1-168 1-168 1-154 1-160 1-182 1-178 1-174 1-170 1-166 1-162 1-168 1-154 1-149 1-146 1-141 1-172 1-168 1-164 1-160 1-156 1-162 1-148 1-144 1-140 1-136 1-132 1-161 1-158 1-164 1-160 1-146 1-142 1-139 1-135 1-180 1-127 1-128 1-161 1-147 1-144 1-140 1-136 1-132 1-129 1-126 1-121 1-118 1-114 1-139 1-136 1-183 1-130 1-126 1-123 1-119 1-116 1-112 1-109 1-105 1-129 1-126 1-123 1-120 1-116 1-113 1-110 1-106 1-103 1-100 1-096 ' 1-118 1-116 1-112 1-110 1-107 1-104 1-101 1-097 1-094 1-091 1-087 1-108 1-190 1-102 1-100 1-097 1-094 1-091 1-088 1-085 1-082 1-079 1-098 1-096 1-092 1-090 1-087 1-084 1-081 1-078 1-076 1-073 1-070 1-088 1-085 1-082 1-080 1-077 1-074 1-071 1-068 1-065 1-063 1-060 1-077 1-075 1-072 1-070 1-067 1-064 1-061 1-068 1-066 1-054 1-061 1-067 1-064 1-062 1-060 1-057 1-065 1-062 1-050 1-048 1-046 1-048 1-057 1054 1-052 1-060 1-047 1-046 1-048 1-040 1-038 1-085 1-033 1-047 1044 1-042 1-040 1-087 1-035 1-033 1-080 1-028 1-025 1-023 1-037 1-034 1-032 1-080 1-027 1-025 1-023 1-020 1-018 1-015 1-013 1-027 1-024 1-022 1-020 1-017 1-015 1-013 1-010 1-008 1-005 1-008 1-017 1-014 1-012 1-010 1-007 1-005 1-008 1-000 0-998 0-996 0093 202 THE TECHNICAL CHEMISTS' HANDBOOK INPLUBNCB OF TEMPBRATUBB ON THB SPBCIFIO GRAVITY OP NITRIC ACID— Continued. 60' 70° 76- 1'336 1-327 1-319 1-310 1-302 1-294 1-286 1-278 1-269 1-261 1-263 1-244 1-234 1-226 1-216 1-206 1-198 1-187 1-177 1-168 1-168 1-160 1-141 1-132 1-124 1-116 1-107 1-099 1-090 1-081 1-073 1-064 1-066 1-046 1-088 1-028 1-018 1-008 0-999 0-989 1-329 1-320 1-312 1-304 1-296 1-288 1-280 1-272 1-264 1-266 1-248 .^-239 1-229 1-220 1-210 1-201 1-191 1-1S2 1-172 1-163 1-164 1-146 1-137 1-128 1-120 1-112 1-103 1-094 1-086 1-078 1-070 1-061 1-062 1-044 1-036 1-026 1-016 1-006 0-997 5-987 1-323 1-314 1-305 1-298 1-290 1-282 1-274 1-266 1-258 1-251 1-243 1-234 1-224 1-216 1-205 1-196 1-186 1-177 1-167 1-160 1-150 1-141 1-133 1-124 1-116 1-108 1-100 1-091 1-083 1-076 1-067 1-068 1-050 1-042 1-034 1-024 1-014 1-004 0-995 0-985 1-316 1-308 1-300 1-292 1-284 1-276 1-268 1-261 1-253 1-246 1-238 1-229 1-219 1-210 1-200 1-191 1-181 1-172 1-163 1-164 1-145 1-136 1-128 1-120 1-112 1104 1-096 1-088 1-080 1-072 1-064 1-055 1-047 1-089 1-031 1-021 1-011 1-001 0-992 0-982 1-SlO 1-302 1-293 1-286 1-278 1-270 1-263 1-256 1-248 1-240 1-232 1-223 1-214 1-205 1-195 1-186 1-177 1-168 1-158 1-149 1-140 1-182 1-124 1-116 1-108 1-100 1-093 1-084 1-076 1-068 1-061 1-052 1-044 1-037 1-029 1-019 1-009 0-999 0-990 0-980 1-303 1-294 1-286 1-279 1-272 1-266 1-267 1-260 1-243 1-236 1-227 1-218 1-209 1-199 1-190 1-181 1-172 1-163 1-153 1-144 1-136 1-128 1-120 1-113 1-105 1-097 1-090 1-OSl 1-073 1-066 1-058 1-050 1-042 1-034 1-026 1-015 1-007 0-997 0-988 0-978 1-296 1-288 1-280 1-274 1-266 1-269 1-252 1-245 1-238 1-230 1-222 1-218 1-204 1-195 1-185 1-176 1-167 1-158 1-148 1-140 1-181 1-123 1-116 1-108 1-101 1-096 1-086 1-078 1-070 1-063 1-055 1-048 1-040 1-031 1-028 1-014 1-004 0-994 0-985 0-97S 1-290 1-282 1'274 1-267 1-260 1-268 1-246 1-240 1-238 1-226 1-217 1-208 1-199 1-190 1-180 1-171 1-162 1-163 1-144 1-135 1-126 1-119 1-112 1-105 1-097 1090 1-082 1-075 1-067 1-060 1-052 1-045 1-088 1-029 1-021 1-012 1-002 0-993 0-983 0-978 NITRIC ACID MANUFACTURE 203 Z. Toted Acidity. — Titrate a diluted sample by standard caustic soda solution. Methyl orange can be quite well used as indicator, if the titration is performed as described^ p. 135, although it would be destroyed by prolonged contact with nitrous acid. Strong fuming acid is weighed in a bulb-tap pipette, Fig. 11, p. 144 ; from this the acid is slowly run on to the bottom of a flask, containing ice-cold water, and the titration is performed quickly, to prevent a decomposition of the nitrous acid. Less concentrated nitric acids may be measured by pipettes or burettes, in lieu of weighing. 4. Chlorine. — Saturate with sodium carbonate, free from chloride, till the reaction is neutral or faintly alkaline, and titrate with silver nitrate according to p. 146. 5. Sidphuric Acid. — Saturate almost completely with sodium carbonate and precipitate with barium chloride as on p. 108. If the acid on evaporating leaves any appreciable fixed residue, this usually consists of sodium sulphate. 6. Nitrous Acid or Nitrogen Tetroxide are estimated by run- ning the acid from a burette into a measured volume of warm, dilute potassium permanganate (c/. p. 135). The result is usually expressed in terms of nitrogen peroxide, N2O4. Each c.c. k normal permanganate =0"023005 g. N2O4. Hence, if m c.c. acid have been used and n c.c. permanganate required, the amount of NjO, is :— 0-023005 n — ^r-^- The quantity of N2O4 is often so considerable that the specific gravity tables give a very deceptive result as to the real percent- age of HNO3, and an actual determination should be made. 7. Fixed Residue, consisting chiefly of sodium sulphate, with a little ferric oxide, etc., is estimated by evaporating to dryness in a place protected from dust, igniting, and weighing. 8. Iron. — Precipitate with excess of ammonia, filter, weigh, and ignite the FeaOg. 9. Iodine is detected by digesting for a short time with pure zinc, which reduces iodic acid and generates some nitrous acid ; the latter sets the iodine of the HI free, and this can then be recognised by shaking up with carbon disulphide, which thereby assumes a pink colour. iV^.5,— Tests Nos. 8 and 9 are only made with nitric acid sold as chemically pure. 204 THE TECHNICAL CHEMISTS' HANDBOOK D. — Mixtures of Sulphuric Acid and Nitric Acid. Such mixtures are sold for the manufacture of explosives and other nitrating purposes. They are analysed by the methods described by Lunge and Berl, Z. angew. Chem., 1905, p. 1681 ; Chem. Zeit., 1907, p. 485. 1. Total Acidity.— Weigh about 1 g. in a bulb-tap pipette. Fig. 11, p. 144, and titrate with normal caustic soda solution. When employing methyl orange as indicator, either add it only towards the end of the titration (or else renew it as destroyed), or else add an excess of soda, then the indicator, and titrate back with normal hydrochloric acid. 2. Nitrous Acid is estimated as on p. 135, by running the mixed acid into a measured quantity of seminormal permanganate. It may be calculated as HNO2, or N2O3, or even as N2O4. In the latter case each c.c. of the ^ normal permanganate indicates 0"023005 g. N2O4. If we caU the c.c. of permanganate used x, the c.c. of mixed acid required for decolorising it y, and s the specific gravity of the latter, the N204is=?^ g. per litre, or ?-^ per cent, by weight of NjOi in the mixed acid. 3. Total Nitrogen Acids are estimated by the nitrometer, p. 137. From the NO given off deduct that corresponding to the nitrous acid found in No. 2, and calculate the remainder as HNO3. 4. Sulphuric Acid is found by deducting the nitrogen acids, found in No. 3, from the total acidity foimd in No. 1. If for 1 g. mixed acid we have used a c.c. ^ normal soda solu- tion and found b c.c. NO (reduced to 0° and 760 mm.), and c c.c. of seminormal permanganate to be required, the percentage of the individual components is found by one of the following formulae, according as to whether we assume N2O4 or N2O3 to be present : — H„SO4 = 0-9808 a -0-219 b H2SO4=0-9808 a -0-219 h HNO3=0-28144 6-3-149c HNOs=0-28144 6-1-6745 c N2O4 =2-30 c NgOs =0-9503 c H2O =100-(H2SO4-l-HNO3 H2O =100-(H2SO4 + HNO3 + N2O4) +N2O3). POTASSIUM SALTS 205 X. POTASSIUM SALTS. A. — Crude Salts (Carnallite, Kainite, etc.). 1. Moisture. — He,at 10 g. to 150° for some time, and allow to cool in a desiccator. 2. Percentage of Potassium :* — (a) In the Absence of more than 0'5 per cent. Potassium Sul- phate. — Obtain a well-mixed sample ; dissolve 7'640 g. in a half -litre flask, fill up to the mark, and filter. Place 20 c.c. of the filtrate (=0"3056 of the crude salt) in a porcelain dish ; add 5 c.c. of a solution of platinum chloride contaming 10 g. Pt. in 100 c.c. Evaporate on the water-bath to a syrupy condition, with frequent agitation, so that most of the HCl is driven ofif and the mass appears dry after cooling. When cool, crush it with a flattened glass rod, add 20 c.c. strong- alcohol (at least 94 per cent.), mix well through and pour the liquid portion through a filter which has been previously dried at 120° to 130° till the weight is constant, then weighed and moistened with alcohol. The filter should not be fiUed up to the top. Pour fresh alcohol on the residue, and heat it on the water-bath nearly to boiling. Wash the solid portion on to the filter, remove most of the liquid by suction, press it between layers of filter paper and dry it till the weight is constant at 120° to 130° (this wiU usually require only twenty ittinutes). Each milligram of the jjotassium -platinum chloride corresponds to O'l per cent. KCl in the quantity of .substance employed. (b) In the Presence of mare than O'bper cent. Potassium Sulphate. — Dissolve 30"56 g. of the crude salt in a J-litre flask in 300 c.c. water -t- 15 cc. strong hydrochloric acid by boiling, allow to cool, and fill the flask up to the mark. Put 50 c.c. of the clear solution into a 200 c.c. flask, heat to boiling, and precipitate the sulphate with the exactly necessary quantity of barium chloride, adding the principal portion of the reagent quickly, the remainder in single drops, always waiting till the liquid shows a clear layer and throwing into this a minute crystal of barium chloride, until this ceases to produce a cloud. If too » These are the methods given by Tietjens in Tech. Meth., vol. i., p. 620, as worlted oat and practised at all the StassfUrt works. This applies also to the figures em- ployed for the calculation of the results which are not based on the real atomic weight of platinum (=19480) and on the formula KaPtOlj, but are empirical data, based on many years' experience. The diflbrence is mainly caused by the fact that the precipitate is not pure KaPtCle, but contains some chemically combined water which is not given up even after prolonged drying. 206 THE TECHNICAL CHEMISTS' HANDBOOK much BaCl2 should have been accidentally added, it must be removed by a drop or two of dilute sulphuric acid. After cooling, fill up to the mark and take 20 c.c. of the clear solution =0'3056 g. salt, which is then treated with platinum chloride as described in No. 1. One mg. of the precipitate corresponds to 0"1 per cent. KCl, if the K is to be calculated as such. For the analysis of salts consisting essentially of K2SO4, like kainite, dissolve 35"71 g., in which case each mg. of the platinum precipitate indicates O'l per cent. K2SO4. When testing rich sulphate (90 to 97 per cent. K2SO4) it is necessary to add to the percentage thus found a correction of +0'3 per cent., but this should not be made ia the case of potasso-magnesium sulphates. 3. Percentage of Sodium Chloride : — (a) In Sigh-Grade Salts. — If there is little or no sul- phate present, the NaCl is calculated from the difference be- tween the KCl found directly by gravimetric analysis and the total chlorides as found by titration with silver solution, p. 147. If there is an appreciable proportion of sulphate present, the percentage of (combined) SO3 must be esti- mated, as well as that of potassium and chlorine. The barium sulphate obtained is calculated to KCl (1 part BaSO4=0'7465 K2SO4=0'6388 KCl); this amount is deducted from the total quantity of K, calculated as KCl ; the remaining KCl, which was present as such and must be quoted as such in the analysis, is deducted from that which is found when calculating aU the CI as KCl. The now remaining nominal amount of KCl is calculated as NaCl, 100 parts KCl being equivalent to 78-41 NaCl. The SO3 found is calculated as K2SO4. (b) In Low-Grade Salts it is not usual to estimate the NaCl. If it is to be done, a complete analysis is required. KCl is esti- mated as above, in addition : Ga (p. 147), Mg (pp. 143 and 207), SO3 (p. 108), insoluble matter, and moisture. SO3 is calculated as CaS04 ; if there is not enough Ca present for all the SO3, the remainder is calculated as MgSO,, and after that as K2SO4. If more Mg is present than is required to saturate the SO3 at dis- posal, the remaining Mg is calculated as MgClj. Any excess of CI over that required to form KCl and MgCl2 is calculated as NaCl. 4. Magnesium Chloride. — In order to distinguish the carnaUite salts (which give up the MgCl2 to alcohol) from the non-carnaUitic salts (which do not do this), shake 10 g. of the crude salt for ten minutes in a ^-litre flask with 100 c.c. 96 per cent, alcohol and titrate 10 c.c. of the filtrate with ^ normal silver solution. Such salts as contain upwards of 6 per cent. CI soluble in alcohol are regarded as belonging to the carnallite group. POTASSIUM SALTS 207 _ 5. Total Magnesium. — Boil 10 g. of finely ground, crude salt with 300 c.c. of water in a |-litre flask for an hour ; after cooling add 50 c.c. twice-normal sodium hydroxide solution, in the case of much lime being present also 20 c.c. of a 10 per cent, solution of neutral potassium oxalate, fill the flask up to the mark, filter after a quarter of an hour, and titrate 50 c.c. of the filtrate by normal hydrochloric acid. Each c.c. of the twice-normal alkali used up is=0'04032 g. MgClj. To the percentage of MgO 0'2 per cent, should be added (Precht. Z. arud. Chem., 1879, p. 438). B. — Commercial Potasslimi Chloride. Weigh out 7'640 g. and proceed exactly as described under A, 2 (a), p. 205_. The calculation is also made in the same manner. Potassium chloride made from vinasses contains much sulphate and a little carbonate, which is estimated alkalimetrically. C. — PotasslTUu Sulphate. Proceed just as in the case of sodium sulphate, p. 148. The potassium must sometimes be estimated, which is done as on p. 205 for A, 2 (b). D. — Leblauc Process for the Manufacture of Potassium Carbonate. Both the raw materials and the intermediate products are tested like those for the soda process, pp. 166 et seg. B. — Beet Ashes. For this material, which seldom occurs in the English trade, special methods have been worked out by Heyer (Ghemiker- Zeitung, 1891, p. 1489 et seq.), and by Alberti and Hempel (ibid., p. 1623). P. — Commercial Carbonate of Potash. 1. Available Alkali is titrated with normal hydrochloric acid, as on p. 178. 2. Total Potassium is estimated according to p. 205, A (b), so that all sulphate is converted into chloride. Of course, initially. 208 THE TECHNICAL CHEMISTS' HANDBOOK more hydrochloric acid must be employed in order to decompose the carbonate. 3. Chloride is estimated by decinormal silver solution, p. 146. 1 CO. of this =0-007456 g. KCl. 4. Sulphate is estimated as BaSOi, p. 109. 1 g. BaSO4=0"7465 K2SO4. 5. Insoluble matter, as on p. 178. 6. Silicate. — Saturate the salt with hydrochloric acid, evaporate to dryness, moisten with HCl, evaporate again, dissolve in dilute HCl, filter, wash, and strongly ignite the SiOj. This test is only made exceptionally, and the potassium silicate is calculated together with the carbonate. 7. Phosphate is estimated by the magnesia method, and is treated like the silicate. 8. Calculation of the Analyses. — Calculate : — (a) K2CO3 from the difference between the total potassium and that corresponding to the CI and SO3 found. (b) NajCOa from the difference between the total available alkali and the K2CO3 as calculated in (a). (c) KCl and (d) K2SO4 as above. (e) Water and (/) Insoluble matter, if necessary also iron, by a special test. POTASSIUM SALTS 209 1. SPBOIPIO GRAVITIES OP SOLUTIONS OP POTASSIUM CARBONATE AT 16°. Specific Degrees Degrees Per cent. X cb.m. contains Gravity. Twaddell. Baum6. KaCOj. kg. K2CO3. 1-000 1-005 1 0-7 0-50 5-0 1-010 2 1-4 1-04 - 10-50 1-015 3 2-1 1-60 16-24 1-020 4 2-7 2-10 21-42 1-025 5 3-4 2-64 27-06 1-030 6 4-1 3-21 33-06 1-035 7 4-7 3-77 39-02 1-040 8 5-4 4-34 45-14 1-045 9 6-0 4-90 51-21 1-050 10 6-7 5-47 57-44 1-055 11 7-4 6-00 63-30 1-060 12 8-0 6-50 68-90 1-065 13 8-7 7-07 75-30 1-070 14 9-4 7-60 81-32 1-075 15 10-0 8-10 87-08 1-080 16 10-6 8-67 93-64 1-085 17 11-2 9-20 99-82 1-090 18 11-9 9-70 105-73 1-095 19 12-4 10-20 111-69 1-100 20 13-0 10-70 117-70 1-105 21 13-6 11-26 124-42 1-110 22 14-2 11-80 130-98 1-115 23 14-9 12-30 137-15 1-120 24 15-4 12-80 143-36 1-125 25 16-0 13-30 149-63 1-130 26 16-5 13-80 155-94 1-135 27 17-0 14-30 162-31 1-140 28 17-7 14-80 168-72 1-145 29 18-3 15-30 175-19 1-150 30 18-8 15-80 181-70 1-155 31 19-3 16-30 188-27 1-160 32 19-8 16-80 194-88 1-165 33 20-3 17-30 201-55 1-170 34 20-9 17-80 208-26 1-175 35 21-4 18-30 215-03 1-180 36 22-0 18-80 221-84 1-185 37 22-5 "19-26 228-23 210 THE TECHNICAL CHEMISTS' HANDBOOK SPBOIPIC GRAVITIES OP SOLUTIONS OP FOTASSIUKI CARBONATE! AT 16° — Continued. Speciflo Degrees Degrees Per cent. 1 cb.m. contains Gravity. Twaddell. Baumd. K2CO3. kg. KaCOs. 1-199 38 23-0 19-70 234-43 1-195 39 23-5 20-20 241-39 1-200 40 24-0 20-70 248-40 1-205 41 24-5 21-15 254-86 1-210 42 25-0 21-60 261-36 1-215 43 25-5 22-05 267-91 1-220 44 26-0 ' 22-50 274-50 1-225 45 26-4 22-96 281-26 1-230 46 26-9 23-41 287-94 1-235 47 27-4 23-90 295-17 1-240 48 27-9 24-40 302-56 1-245 49 28-4 24-86 309-51 1-250 50 28-8 25-32 316-50 1-255 51 29-3 25-80 323-79 1-260 52 29-7 26-30 331-38 1-265 53 30-2 26-77 338-64 1-270 54 30-6 27-17 345-06 1-275 55 31-1 27-60 351-90 1-280 66 31-5 28-05 359-04 1-285 67 32-0 28-50 366-23 1-290 58 32-4 28-96 373-58 1-295 59 32-8 29-42 380-99 1-300 60 33-3 29-97 389-61 1-305 61 33-7 30-43 397-11 1-310 62 34-2 30-86 404-27 • 1-315 63 34-6 31-24 ^10-81 1-320 64 35-0 31-60 417-12 1-325 65 35-4 32-06 424-80 1-330 66 35-8 32-52 432-52 1-335 67 36-2 32-96 440-02 1-340 68 36-6 33-38 447-29 1-345 69 37-0 33-80 454-61 1-350 70 37-4 34-22 461-97 1-355 71 37-8 34-64 469-37 1-360 72 38-2 35-06 476-82 1-365 73 38-6 ■ 35-48 484-30 1-370 74 39-0 35-90 491-83 POTASSIUM SALTS 211 SPECIFIC GRAVITIES OF SOLUTIONS OF POTASSIUM CARBONATE AT 15°— Continued. Specific Degress Degrees Per cent. Icb.m. contains Gravity. Twaddell. Bsum6. KaCOs. kg. K2CO3. 1-375 75 39-4 36-32 499-40 1-380 76 39-8 36-74 507-01 1-385 77 40-1 37-17 614-80 1-390 78 40-5 37-60 622-64 1-395 79 40-8 38-02 530-38 1-400 80 41-2 38-45 538-30 1-405 81 41-6 38-88 546-26 1-410 82 42-0 39-30 554-13 1-415 83 42-3 39-73 562-19 1-420 84 42-7 40-16 570-27 1-425 85 43-1 40-59 578-41 1-430 86 43-4 41-02 586-59 1-435 87 43-8 41-45 594-81 1-440 88 44-1 41-85 602-64 1-445 89 44-4 42-22 610-08 1-450 90 44-8 42-58 617-41 1-455 91 45-1 42-97 625-21 1-460 92 45-4 43-37 633-20 1-465 93 45-8 43-77 641-23 1-470 94 46-1 44-17 649-30 1-475 95 46-4 44-57 657-41 1-480 96 46-8 44-96 665-41 1-485 97 47-1 45-38 673-89 1-490 98 47-4 45-81 682-57 1-495- 99 47-8 46-24 691-29 1-500 100 48-1 46-66 699-90 1-505 101 48-4 47-03 707-80 1-510 102 48-7 47-40 715-74 1-515 103 49-0 47-78 723-87 1-520 104 49-4 48-15 731-88 1-525 105 49-7 48-53 740-08 1-530 106 50-0 48-90 748-17 1-535 107 60-3 49-26 766-14 1-540 108 50-6 49-61 763-99 1-545 109 60-9 49-96 771-88 1-550 110 51-2 50-33 780-12 1-555 111 ■ 51-5 50-70 788-39 1-560 112 51-8 51-07 796-69 1-565 113 52-1 61-45 805-19 212 THE TECHNICAL CHEMISTS' HANDBOOK 2. INPLTJBNOB OP TEMPERATURE ON THE SPHCIPIO O'O. 6°. 10-. 15°. 20°. 25". 30°. 35°. 40°. 45°. 60°. 1-688 1-586 1-683 1-580 1-577 1-674 1-671 1-66S 1-566 1-563 1-569 1-677 1-676 1-673 1-670 1-508 1-666 1-663 1-660 1-567 564 1-661 1-667 1-566 1-563 1-660 1-668 1-566 1-663 1-660 1-648 645 1-643 1-667 1-554 1-562 1-650 1-548 1-546 1-644 1-641 1-538 686 1-633 1-647 1-544 1-642 1-540 1-538 1-536 1-684 1-631 1-528 526 1-623 1-635 1-53* 1-632 1-630 1-628 1-520 1-524 1-621 1-618 616 1-512 1-626 1-524 1-622 1-620 1-518 1-516 1-514 1-611 1-508 506 1-602 1-616 1-614 1-612 1-610 1-608 1-606 1-503 1-600 1-498 496 1-492 1-506 1-504 1-502 1-600 1-498 1-496 1-493 1-490 1-488 486 1-482 1-496 1-494 1-492 1-490 1-488 1-486 1-484 1-481 1-478 476 1-472 1-486 1-484 1-482 1-480 1-478 1-476 1-474 1-471 1-468 466 1-462 1-476 1-474 1-472 1-470 1-468 1-466 1-464 1-461 1-468 455 1-452 1-466 1-464 1-462 1-460 1-468 1-466 1-464 1-451 1-448 445 1-442 1-466 1-464 1-462 1-460 1-448 1-446 1-444 1-441 1-438 436 1-432 1-446 1-444 1-442 1-440 1-438 1-436 1-484 1-431 1-428 425 1-422 1-436 1-434 1-432 1-430 1-428 1-426 1-424 1-420 1-418 414 1-411 1-426 1-424 1-422 1-420 1-418 1-416 1-414 1-410 1-408 404 1-401 1-416 1-414 1-412 1-410 1-408 1-406 1-404 1-401 1-398 395 1-392 1-406 1-404 1-402 1-400 1-898 1-396 1-394 1-391 1-3S8 385 1-382 1-396 1-394 1-392 1-390 1-388 1-386 1-384 1-881 1-378 376 1-373 1-386 1-384 1-382 1-380 1-878 1-376 1-374 1-871 1-368 366 1-363 1-376 1-374 1-872 1-370 1-868 1-366 1-364 1-861 1-35S 356 1-36S 1-366 1-364 1-362 1-360 1-358 1-366 1-364 1-351 1-348 346 1-843 1-356 1-354 1-352 1-360 1-848 1-346 1-344 1-341 1-338 336 1-333 1-346 1-344 1-342 1-340 1-838 1-386 1-884 1-331 1-328 326 1-323 1-336 1-334 1-332 1-830 1-828 1-326 1-824 1-321 1-818 316 1-313 1-326 1-324 1-822 1-320 1-318 1-316 1-314 1-311 1-308 306 1-303 1-816 1-314 1-312 1-310 1-308 1-306 1-303 1-300 1-298 296 1-292 1-306 1-304 1-302 1-300 1-298 1-296 1-293 1-290 1-288 286 1-282 1-296 1<294 1-292 1-290 1-288 1-286 1-283 1-280 1-278 275 1-273 1-286 1-284 1-282 1-280 1-278 1-276 1-278 1-270 1-268 266 1-263 1-276 1-274 1-272 1-270 1-268 1-265 1-263 1-260 1-267 265 1-262 1-266 1-264 1-262 1-260 1-258 1-266 1-253 1-250 1-247 245 1-242 1-266 1-264 1-262 1-250 1-248 1-246 1-243 1-240 1-288 235 1-232 1-246 1-244 1-242 1-240 1-238 1-236 1-238 1-230 1-228 226 1-222 1-236 1-234 1-232 1-230 1-228 1-226 1-224 1-222 1-219 217 1-214 1-226 1-224 1-222 1-220 1-218 1-216 1-214 1-212 1-209 207 1-204 1-216 1-214 . 1-212 1-210 1-208 1-206 1-204 1-202 1-109- 197 1-194 1-206 1-204 1-202 1-200 1-198 1-196 1-194 1-192 1-189 187 1-184 1-196 1-194 1-192 1-190 1-188 1-186 1-184 1-182 1-179 177 1-174 1-186 1-184 1-182 1-180 1-178 1-176 1-174 1-172 1-170 167 1-164 1-175 1-173 1-171 1-170 1-168 1-166 1-164 1-162 1-160 167 1-155 1-165 1-163 1-161 1-160 1-158 1-156 1-164 1-152 1-150 147 1-145 1-166 1-163 1-151 1-160 1-148 1-146 1-144 1-142 1-140 137 1-136 1-144 1-143 1-141 1-140 1-138 1-136 1-134 1-182 1-130 127 1-125 1-183 1-132 1-131 1-130 1-128 1-126 1-124 1-122 1-120 117 1-114 1-123 1-122 1-121 1-120 1-118 1-116 1-114 1-112 1-110 107 1-104 1-113 1-112 1-m 1-110 1-108 1-106 1-104 1-102 1-100 097 1-094 1-103 1-102 1-101 1-100 1-098 1-096 1-094 1-002 1-090 087 1-0S4 1-093 1-092 1-091 1-000 1-089 1-087 1-0S6 1-083 1-081 079 1-077 1-083 1-082 1-081 1-080 1-079 1-077 1-076 1-073 1-071 069 1-067 1-073 1-072 1-071 1-070 1-069 1-067 1-066 1-004 1-062 060 1-068 1-068 1-062 1-061 1-060 1-069 1-067 1-060 1-064 1-063 060 1-048 1-063 1-052 1-051 1-060 1-049 1-047 1-046 1-044 1-042 040 1-038 1-043 1-042 1-041 1-040 1-039 1-037 1-036 1-034 1-032 030 1-028 1-033 1-032 1-031 1-080 1-028 1-027 1-025 1-024 1-022 020 1-018 1-023 1022 1-021 1-020 1-018 1-017 1-016 1-014 1-012 010 1-008 1-013 1-012 1-011 1-010 1-008 1-007 1-005 1-004 1-002 1-000 0-998 POTASSIUM SALTS 213 GRAVITIES OP SOLUTIONS OP POTASSIUM GABBONATB. ,66-. 60°. 66". 70°. 75°. 80°. 85°. 90°. 96°. 100°. 1-566 1-563 1-560 1-646 1-542 1-588' 1-534 1-580 1-626 1-621 1-64S 1-645 1-641 1-687 1-633 1-530 1-626 1-522 1-518 1-513 1-689 1-536 1-582 1-528 1-626 1-622 1-617 1-518 1-609 1-606 1-530 1-527 1-624 1-621 1-617 1-513 1-509 1-504 1-601 1-498 1-620 1-617 1-514 1-511 1-608 1-504 1-600 1-407 1-494 1-490 1-609 1-507 1-604 1-600 1-497 1-494 1-491 1-488 1-485 1-481 1-499 1-497 1-494 1-490 1-487 1-484 1-481 1-478 1-475 1-471 1-4S0 1-487 1-484 1-4S0 1-477 1-474 1-471 1-468 1-465 1-461 1-479 1-470 1-474 1-470 1-467 1-464 1-461 1-458 1-465 1-451 1-469 1-466 1-464 1-460 1-457 1-464 1-460 1-447 1-444 1-441 1-469 1-466 1-464 1-450 1-447 1-444 1-440 1-437 1-484 1-431 1-449 1-446 1-444 1-440 1-487 1-434 1-431 1-428 1-424 1-421 1-439 1-436 1-434 1-480 1-427 1-424 1-421 1-418 1-414 1-411 1-429 1-426 1-428 1-420 1-417 1-414 1-410 1-408 1-406 1-402 1-419 1-416 1-418 1-410 1-407 1-404 1-400 1-898 1-396 1-892 1-409 1-406 1-404 1-401 1-898 1-396 1-301 1-388 1-386 1-382 1-399 1-396 1-394 1-891 1-8SB 1-385 1-881 1-37S 1-876 1-372 1-390 1-387 1-384 1-880 1-877 1-374 1-371 1-368 1-366 1-862 1-380 1-877 1-374 1-370 1-867 1-364 1-361 1-368 1-356 1-852 1-870 1-367 1-364 1-861 1-368 1-356 1-351 1-848 1-345 1-842 1-360 1-367 1-364 1-351 1-848 1-346 1-341 1-388 1-836 1-332 1-350 1-347 1-344 1-341 1-338 1-385 1-332 1-329 1-326 1-323 1-340 1-337 1-334 1-331 1-328 1-826 1-322 1-319 1-816 1-313 1-3S0 1-327 1-324 1-821 1-318 1-816 1-812 1-309 1-306 1-303 1-320 1-B17 1-314 1-311 1-308 1-306 1-802 1-299 1-296 1-293 1-310 1-307 1-S04 1-301 1-298 1-296 1-292 1-289 1-2S6 1-284 1-300 1-207 1-294 1-201 1-288 1-286 1-282 1-279 1-276 1-274 1-290 1-287 1-2S4 1-281 1-278 1-276 1-273 1-270 1-267 1-264 1-2S0 1-277 1-274 1-271 1-268 1-266 1-263 1-260 1-267 1-264 1-270 1-267 1-264 1-261 1-268 1-266 1-268 1-250 1-247 1-244 1-260 1-257 1-264 1-251 1-248 1-246 1-243 1-240 1-237 1-234 1-260 1-247 1-244 1-242 1-239 1-236 1-234 1-281 1-228 1-225 1-240 1-237 1-234 1-282 1-229 1-226 1-224 1-221 1-218 1-215 1-230 1-227 1-224 1-221 1-218 1-216 1-218 1-210 1-208 1-205 1-220 1-217 1-214 1-211 1-208 1-206. 1-208 1-200 1-198 1-196 1-212 1-209 1-206 1-202 1-198 1-196 1-194 l"l92 1-188 1-186 1-202 1-199 1-196 1-198 1-190 1-187 1-184 1-182 1-178 1-176 1192 1-189 1-186 1-183 1-180 1-178 1-176 1-172 1-169 1-167 1-182 1-179 1-176 1-173 1-171 1-168 1-165 1-162 1-159 1-167 1-172 1-169 1-166 1-164 1-161 1-158 1-165 1-152 1-149 1-146 1-162 1-169 1-156 1-164 1-161 1-148 1-145 1-142 1-139 1-186 1-162 1-150 1-147 1-144 1-141 1-188 1-185 1-182 1-120 1-126 1-142 1-140 1-187 1-134 1-181 1-128 1-125 1-122 1-119 1-116 1-132 1-130 1-128 1-126 1-122 1-118 1-115 1-112 1-109 1-106 1-122 1-120 1-118 1-116 1-112 1-108 1-106 1-102 1-099 1-096 1-112 1-110 1-108 1-106 1-102 1-098 1-096 1-092 1-089 1-086 1-102 1-100 1-098 1-096 1-092 1-088 1-086 1-082 1-078 1-076 1-092 1-090 1-087 1-084 1-082 1-079 1-076 1-072 1-069 1-067 1-082 1-080 1-077 1-074 1-072 1-069 1-065 1-062 1-059 1-057 1-074 1-071 1-068 1-066 1-063 1-060 1-067 1-054 1-060 1-048 1-068 1-062 1-059 1-068 1-054 1-051 1-048 1-045 1-041 1-038 1-056 1-053 1-060 1-047 1-046 1-042 1-089 1-036 1-082 1-029 1-046 1-044 1-041 1-088 1-036 1-038 1-030 1-020 1-028 1-020 1-036 1-033 1-031 1-028 1-026 1-022 1-019 1-016 1-018 1-010 1-026 1-023 1-021 1-018 1-016 1-012 1-009 1-006 1-003 1-000 I-Olfl 1-014 1-012 1-009 1-006 1-002 0-999 0-906 0-998 0-990 1-007 1-004 1-002 0-999 0-996 0-993 0-990 0-987 0-984 0-981 0-996 0-994 0-992 0-989 0-986 0-983 0-980 0-977 0-974 0-971 2U THE TECHNICAL CHEMISTS' HANDBOOK 8. SPECIFIC GRAVITY OP SOLUTIONS OP POTASSIUM 15° 4° obtained, by Pickering {Joum. Chem. Soc, Ixlii., 890). HITDBOXIDB AT Calculated £rom the results 100 parts by weight contain 1 cb.m. contains kK. Speetflo Gravity. Degrees TwaddeU. Degrees Baum6. KgO. KOH. KaO. KOH. 1-000 0-00 0-00 0-00 0-00 1-005 1 0-7 0-50 0-60 5-03 6-03 1-010 2 1-4 0-99 1-18 10-00 11-92 1-015 3 2-1 1-45 1-73 14-72 17-56 1-020 4 2-7 1-91 2-28 19-48 23-26 1-025 5 3-4 2-37 2-82 24-29 28-91 1-030 6 4-1 2-82 3-36 29-05 34-61 1-035 7 4-7 3-27 3-90 33-84 40-37 1-040 8 5-4 3-73 4-44 38-79 46-18 1-045 9 6-0 4-19 4-99 43-79 52-15 1-050 10 6-7 4-64 5-53 48-72 58-07 1-055 11 7-4 5-10 6-08 53-81 64-14 1-060 12 8-0 5-54 6-60 58-72 69-96 1-065 13 8-7 6-00 7-15 63-90 76-15 1-070 14 9-4 6-45 7-68 69-02 82-18 1-075 15 10-0 6-90 8-22 74-18 88-37 1-080 16 10-6 7-35 8-76 79-38 94-61 1-085 17 11-2 7-79 9-28 84-62 100-69 1-090 18 11-9 8-24 9-82 89-82 107-04 1-095 19 12-4 8-68 10-37 95-05 113-22 1-100 20 13-0 9-13 10-87 100-43 119-57 1-105 21 13-6 9-62 11-46 106-30 126-63 1-110 22 14-2 10-00 11-92 110-00 132-31 1-115 23 14-9 10-44 12-44 116-41 138-71 1-120 24 15-4 10-88 12-96 121-86 145-15 1-125 25 16-0 11-32 13-48 127-35 151-65 1-130 26 16-5 11-76 14-01 132-89 158-31 1-135 27 17-0 12-21 14-53 138-58 164-92 1-140 28 17-7 12-63 15-04 143-98 171-46 1-145 29 18-3 13-06 15-56 149-53 178-16 1-150 30 18-8 13-50 16-08 155-25 184-92 1-155 31 19-3 13-92 16-58 160-78 191-50 1-160 32 19-8 14-36 17-10 166-58 198-36 1-165 33 20-3 14-79 17-62 172-30 205-27 1-170 34 20-9 15-22 18-13 178-07 212-12 1-175 L- a^ 35 21-4 15-65 18-64 183-89 219-02 POTASSIUM SALTS 215 SPECIFIC GRAVITY OF SOLUTIONS OF POTASSIUM HYDBO-XTDEl AT -^ s — Gontirmed. 100 parts by weight 1 cb.m. contains Itg. Specific Degrees Twaddell. Degrees Bauni6. con Gravity. K2O KOH. K2O. KOH. V180 36 22-0 16-08 19-15 189-74 225-97 1-185 37 22-5 16-51 19-66 195-64 232-97 1-190 38 23-0 16-93 20-17 201-47 240-02 1-195 39 23-5 17-35 20-66 207-33 246-89 1-200 40 24-0 17-77 21-17 213-24 254-04 1-205 41 24-5' 18-18 21-66 219-07 261 -00 1-210 42 25-0 18-60 22-16 225-06 268-14 1-215 43 25-5 19-03 22-67 231-21 275-44 1-220 44 26-0 19-45 23-17 237-29 282-67 1-225 45 26-4 19-86 23-66 243-29 289-84 1-230 46 26-9 20-27 24-14 249-32 296-92 1-235 47 27-4 20-69 24-64 255-52 304-30 1-240 48 27-9 21-10 25-13 261-64 311-61 1-245 49 28-4 21-51 25-62 267-80 318-97 1-250 50 28-8 21-91 26-10 273-88 326-25 1-255 51 29-3 22-32 26-59 280-12 333-70 1-260 52 29-7 22-73 27-07 286-40 341-08 1-265 53 30-2 23-14 27-56 292-72 348-63 1-270 54 30-6 23-54 28-04 298-96 356-11 1-275 55 31-1 23-94 28-52 305-24 363-63 1-280 56 31-5 24-35 29-00 311-68 371-20 1-285 57 32-0 24-75 29-48 318-04 378-82 1-290 58 32-4 25-15 29-96 324-44 386-48 1-295 59 32-8 25-55 30-43 330-87 394-07 1-300 60 33-3 25-95 30-91 337-35 401-83 1-305 61 33-7 26-34 31-37 343-74 409-38 1-310 62 34-2 26-73 31-84 350-16 417-10 1-315 63 34-6 27-13 32-31 356-76 424-88 1-320 64 35-0 27-52 32-78 363-26 432-70 1-325 65 35-4 27-91 33-24 369-81 440-43 1-330 66 35-8 28-29 33-70 376-26 448-21 1-335 67 36-2 28-68 34-16 382-88 456-04 1-240 68 36-6 29-07 34-63 389-54 464-04 1-345 69 37-0 29-46 35-09 396-24 471-96 1-350 70 37-4 29-85 35-55 402-98 479-93 1-355 71 37-8 30-23 36-01 409-62 487-94 1-360 72 38-2 30-61 36-46 416-30 495-86 216 THE TECHNICAL CHEMISTS' HANDBOOK SPECIFIC GRAVITY OP SOLUTIONS OF POTASSIUM HYDROXIDE AT— s- — Continued. 100 parts by weight contain 1 cb.m. contains kg. Specific Gravity. Degrees TwaddeU. Degrees Baum6. KjO. KO4. K2O. KO4. 1-365 73 38-6 30-99 36-92 423-01 503-96 1-370 74 39-0 31-37 37-37 429-77 511-97 1-375 75 39-4 31-76 37-83 436-70 520-16 1-380 76 39-8 32-14 38-28 443-63 528-26 1-385 77 40-1 32-52 38-73 450-40 536-41 1-390 78 40-5 32-89 39-18 457-17 644-60 1-395 79 40-8 33-27 39-63 464-12 552-84 1-400 80 41-2 33-66 40-09 471-24 561-26 1-405 81 41-6 34-03 40-53 478-12 669-46 1-410 82 42-0 34-40 40-98 485-04 677-82 1-415 83 42-3 34-77 41-42 492-00 586-09 1-420 84 42-7 35-15 41-87 499-13 594-55 1-425 85 43-1 35-53 42-32 506-30 603-06 1-430 86 43-4 35-90 42-76 513-37 611-47 1-435 87 43-8 36-27 43-20 520-47 619-92 1-440 88 44-1 36-63 43-63 527-47 628-27 1-445 89 44-4 36-99 44-06 534 -51 636-67 1-450 90 44-8 37-36 44-50 541-72 645-26 1-455 91 45-1 37-72 44-93 548-83 653-73 1-460 92 45-4 38-09 45-37 556-11 662-40 1-465 93 45-8 38-45 45-80 563-29 670-97 1-470 94 46-1 38-81 46-23 570-51 679-68 1-475 95 46-4 39-17 46-66 577-76 688-24 1-480 96 46-8 39-54 47-09 585-19 696-93 1-485 97 47-1 39-89 47-51 592-37 705-52 1-490 98 47-4 40-24 47-93 599-68 714-16 1-495 99 47-8 40-60 48-36 606-97 722-98 1-600 100 48-1 40-95 48-78 614-25 731-70 1-505 101 48-4 41-31 49-20 621-72 740-46 1-510 102 48-7 41-68 49-64 629-37 749-66 1-515 103 49-0 42-03 50-06 636-75 758-41 1-520 104 49-4 42-38 50-48 644-18 767-30 1-525 105 49-7 42-73 50-90 651-63 776-23 1-530 106 50-0 43-09 51-32 659-28 785-20 1-535 107 50-3 43-41 SI -74 666-80 794-21 1-540 108 50-6 43-78 62-15 674-2] 803-11 AMMONIA MANUFACTURE 217 XI. AMMONIA MANUFACTURE. A. — Gas-Liquor. This liquor generally contains the ammonia principally in the state of carbonate and sulphide, which can be driven off by boU- ing, without employing lime or alkali, and which are indicated by alkalimetrical testing {volatile ammonia). There is, however, always a certain quantity of ammonia present in the state of salts which are not appreciably volatilised by mere boiling, and not indicated by simple testing with standard acid. These are the chloride, thiocyanate, sulphite, thiosulphate, sulphate, ferro- cyanide {fixed ammonia). No other salts need be enumerated. For technical purposes, it is sufficient to make the following tests : — 1. Volatile Ammonia. — Dilute 20 c.c. of gas-liquor with 100 c.c. water, add 30 c.c. of normal hydrochloric acid, and boil till all CO2 and HjS is expelled. Titrate back with seminormal alkali, employing the ordinary indicators. If the liquor is too much coloured to see the change of the indicator, dilute it with water or employ litmus paper. Or else run 10 c.c. of the gas-liquor into a beaker containing 250 c.c. water, add 2 drops methyl orange solution (1 : 1000), and titrate at once in the cold with normal hydrochloric acid. If the indicator is destroyed by HjS, add another drop of it. Each c.c. of normal acid corresponds to 0-01703 g. NH3, or to 0-08515 parts NH3 by weight, in 100 vols, of gas-liquor : or to 0-4216 ounces of rectified oil of vitriol (of 93 per cent. SO4H2) per gallon of gas-liquor. 2. Total Ammonia. — Put 20 c.c. of gas-liquor, with about as much water, into the flask A, Fig. 17, and charge the receivers B and C with 30 c.c. of normal hydrochloric acid previously diluted to twice its volume. The greater portion of this mixture should be contained in the U-tube B. Make the connection and run 3 c.c. concentrated caustic soda solution into A through the pinch- cock funnel a. Apply heat and keep up a gentle distillation for one or two hours, when all NH3 will be, driven off and absorbed in B and C. Unite the contents of these vessels and titrate back with seminormal caustic soda. If a c.c. of this are used, 30 - -^ 2 indicates the c.c. of acid corresponding to the total ammonia, and calculated as in Test No. 1 . 3. Total Sulphur.— Rxm 50 c.c. of gas-liquor, drop by drop, into bromine, covered by hydrochloric acid, evaporate to dryness 218 THE TECHNICAL CHEMISTS' HANDBOOK on tlie water-bath, and precipitate the sulphuric acid formed by- barium chloride, as described p. 109. Sometimes it may be desirable to deduct from the total sulphur that originally present in the gas-liquor as sulphate, which is estimated by boiling the unoxidised gas-liquor with HCl and proceeding as above. 4. Thiocycmate. — Evaporate 50 c.c. of gas-liquor to diyness, heat the residue at 100° C., for three or four hours, digest it with strong al&hol, filter, wash on the filter with alcohol, evaporate all the alcoholic solutions to dryness, dissolve in water, filter from Fia. 17. any residue, add a mixed solution of sulphurous acid and cupric sulphate, and heat gently, when cuprous thiocyanate will be precipitated. Wash the precipitate of CuCNS into a flask, dissolve it in nitric acid, boil for some time, and precipitate the Cu as CuO by NaOH. The weight of GuOx 0-9561= the equivalent amount of (NH4) CNS (Dyson, S.C.I., 1883, p. 231). Or else proceed by titration, employing a solution containing 6"236 g. CUSO4, SHjO per litre, 1 c.c. of which is equivalent to 0-00145 g. SON =0-00190 g. (NH4) SON, which is added to a boiling solution, to which some sodium bisulphite has been added, till a drop of the mixture, brought into contact with a drop of a solution of potassium f errocyanide in 20 parts of water, produces immediately a brown coloration (Barnes and Liddell, S.Cf.1 , 1883, p. 122). AMMONIA MANUFACTURE 219 B. — Sulphate of Ammoma. 1. Estimation of Ammonia. — The average sample, carefully- drawn, is well ground up, passed completely through a sieve with 10 holes to the linear inch, and a smaller sample is taken from this. Weigh 17 "03 g. of the latter sample in a stoppered tube, dissolve and dilute to 500 c.c, and place 50 c.c. of the solution without filtration into the apparatus. Fig. 17 (p. 218). The test is carried out exactly as in A, No. 2. Each c.c. of the quantity 30--^ is = 0-01703 g. NH3 or = I'O per cent. The analysis of sulphate of ammonia is, however, best, and much more quickly performed by the bromine method, in which the NH3 is converted into nitrogen. This method can be carried out in the " Azoto- meter," or in Lunge's gas-volumeter (p. 139), if the latter is provided with a " decomposing flask," as shown in Fig. 18. The necessary "brominated soda" is prepared by dissolving 100 g. 70 per cent, caustic soda in 1250 g. water, and cautiously adding 25 g. bromine. The reagent must be kept in a dark, cool place, but even then does not keep more than a few days. The am- monium salt, preferably dissolved in water, is introduced into the outer space of the decomposing flask a. Fig. 1 9, and 25 or 30 c.c. brominated soda poured mto the inner vessel b. The cork/, having been already attached to the volumeter-tube by means of 220 THE TECHNICAL CHEMISTS'. HANDBOOK a short rubber tube, is pressed tightly down into the flask a, taking hold of this only by the neck ; the pressure thus produced is relieved by momentarily pulling out the stopper of the volu- meter-tap e. If thereby the mercury in A should sink a little, it is brought back to the zero point by raising the "level-tube," while A communicates through d with the outer air. When the temperatures are equalised and the mercury is up to the tap, this is put in such a position that a communicates through c with A ; then the flask a is tilted so that the contents of b run into the outer space ; the flask is then shaken till no more gas is evolved. The mercury levels in A and the level-tube are made to coincide, after waiting a quarter of an hour, or, better, haM an hour, in order to cool down the flask. (This may be expedited by placing a both before and after the operation, in a large vessel filled with water of the temperature of the room.) When the levels have been exactly adjusted, as described p. 141, so as to bring the gas to the volume it would occupy at 0° and 760 mm. in the dry state, read offthe number of c.c. of gas in A; eachc.c.=0'0012818g. N'=0'0015582 g. NH3 (this includes the necessary correction for absorption or incomplete evolution of N). In order to save all calculations, dissolve 1'558 g. sulphate of ammonia in 100 c.c. of water, and employ 10 c.c.=0"1558 g. for each test; in this case each c.c. of gas contained in A=l per cent. NH3. 2. Thiocycmate.—Cf. p. 118, A, No. 4. 3. Free Acid is found by titration with decinormal soda solution and methyl orange. 4. Moisture is estimated by drying 50 g. in a stove at 100° up to constancy of weight. C. — Liquor Aiumonise. This is mostly sold bjr specific gravity, the relation of which to the percentage of NH3 is shown in the subjoined table No. 1. The empyreumatic substances in liquor ammonise are detected qualitatively by the smell on exact neutralisation with sulphuric acid. The pyridine bases (which do not redden phenolphthalein) can be tested for by the method of Pennock and Morton (Journ. Amer. Chem. Soc, vol. xxiv., p. 377). Neutralise 100 c.c. of the liquor exactly by sulphuric acid, employing methyl orange as indicator and cooling the vessel used from the outside ; distil into a flask charged with 30 c.c. water until this volume has increased to about 100 c.c, add phenolphthalein and a solution of mercuric chloride until the liquid is decolorised, then a few more drops of the mercury solution (thereby precipitating the NH3), filter, and titrate with decinormal acid and methyl orange, each c.c. of which =0'0079 g. pyridine. The testing of liquid ammonia, as sent out in iron bottles, is described in Tech. Meth., vol. ii. AMMONIA MANUFACTURE 221 1. SPBOIPIO GRAVITIES OF SOLUTIONS OP AMMONIA AT 15°. (Iiunse and WiernUr.) Speoiflc Gravity. Per cent. NH3. 1 litre contains grams NH3 at 15°. CoiTection of specific gravity for ± 1" C. 1-000 0-00 0-00 0-00018 0-995 1-14 11-34 0-00019 0-990 2-31 22-87 0-00020 0-985 3-55 34-97 0-00021 0-980 4-80 47-04 0-00023 0-975 6-05 58-99 0-00024 0-970 7-31 70-91 0-00025 0-966 8-59 82-89 0-000265 0-960 9-91 95-13 0-00029 0-955 11-32 108-11 0-000:n5 0-950 12-74 121 -03 0-00034 0-945 14-17 133-91 0-000365 0-940 15-63 146-92 0-00039 0-935 17-12 160-07 0-00041 0-930 18-64 173-35 0-00042 0-925 20-18 186-67 0-000445 0-920 21-75 200-10 0-00047 0-915 23-35 213-65 0-000495 0-910 24-99 227-41 0-00052 0-905 26-64 241 -09 0-000515 0-900 28-33 254-97 0-00057 0-895 30-03 268-77 0-000595 0-890 31-73 282-40 O-O11O6I 0-885 33-67 297-98 0-000635 0-880 35-60 313-28 0-00066 222 THE TECHNICAL CHEMISTS' HANDBOOK 2. SPBOIPIC GRAVITIES OF SOLUTIONS OF COMMERCIAL AMMONIUM CARBONATE, AT 15° C. (Lunge ana Smith.) Degrees Degrees Specific Gravity Per cent. Commercial Change of Specific Gravity tor ± !• C. TwaddeU. Banm6. at 15°. Aramoniam Car- bonate. 1 0-6 1-005 1-66 0-0002 2 1-4 1-010 . 3-18 0-0002 3 2-1 1-015 4-60 0-0003 4 2-7 1-020 6-04 0-0003 5 3-4 1-025 7-49 0-0003 6 4-1 1-030 8-93 0-0004 7 4-7 1-035 10-35 0-0004 8 5-4 1-040 11-86 0-0004 9 6-0 1-045 13-36 0-0005 10 6-7 1-050 14-83 0-0005 11 7-4 1-055 16-16 0-0005 12 8-0 1-060 17-70 0-0005 13 8-7 1-065 19-18 0-0005 14 9-4 1-070 20-70 0-0005 15 10-0 1-075 22-25 0-0006 16 10-6 1-080 23-78 0-0006 17 11-2 1-085 25-31 0-0007 18 11-9 1-090 26-82 0-0007 19 12-4 1-095 28-33 0-0007 20 13-0 1-100 29-93 0-0007 21 13-6 1-105 31-77 0-0007 22 14-2 1-110 33-45 0-0007 23 14-9 1-115 35-08- 0-0007 24 15-4 1-120 36-88 0-0007 25 16-0 1-125 38-71 0-0007 26 16-5 1-130 40-34 0-0007 27 17-1 1-135 42-20 0-0007 28 17-8 1-140 44-29 0-0007 29 17-9 1-1414 44-90 0-0007 XII. MANUFACTURE OP COAL-GAS (ILLUMINATING GAS). A. — Coal-Gas. For a satisfactory analysis of coal-gas the Orsat apparatus (p. 95) is not sufBcieatly accurate, and the gas-burettes of Bunte, Hempel, Drehschmidt, or Pfeiffer should be used. The following MANUFACTURE OF COAL-GAS 223 rules are taken from the private notes, printed for Professor Bunte's students, with his permission. The analysis is performed by means of Bunte burettes, which must satisfy the following conditions : — The capillary tube below the bottom tap must not allow any water to come out, even on shaking. The upper (three-way) tap must be made so as to shut off communication with any one of the three outlets. (The Greiner- Friedrichs patent tap, with two oblique bores, as shown in Fig. 16, p. 171, admits of doing .this without any difficulty.) The taps should be greased with a mixture of 2 parts para-gum, 2 parts bees- wax, and 10 parts taUow, and they must be tight even in a strong vacuum. The coniining water must have the temperature of the room, and this must remain unchanged during the whole time occupied by the work. The burette must be held only at the top funnel or at the capUlary tubes. The correctness of its graduation must be controlled by running out its contents of water in portions of 10 c.c, and weighing these. When one of the components of the gas has been absorbed, first allow the water to rise from below and then adjust the pressure by allowing water to run in from the top funnel. To do this, fill it to the mark, open the tap and wait a minute, until the surface of the water inside the burette remains constant. To take a sample of the gas to he tested, employ either an empty burette, or one filled with water. In the former case, connect the top tap (the funnel being charged with water) side- ways with the gasholder or pipe, the bottom tap being open, and allow the gas to pass through, until it has driven out aU the air ; then shut first the bottom tap and immediately afterwards the top tap. In the second case faU the burette with water, connect the top tap vidth the gasholder or pipe, open the bottom tap, until the water has sunk a little below the zero mark, then shut first the top tap and afterwards the bottom tap. If the gas is at a lower pressure than the atmospheric pressure, take the sample by means of a rubber bellows, or a water aspirat- ing bottle, or a water-pump, and connect then with the bottom capillary. Measuring the gas in the burette. — Adjust the three-way tap so that all its bores are closed, fill the funnel with water up to the mark, connect the rubber tube of the pressure bottle (levelling bottle), previously entirely fiUed with water, with the bottom tap, and allow the water to rise up to about 0'2 c.c. above the zero mark. Now open the three-way tap, whereupon a little gas escapes and the pressures are equalised. The water then usually stands at the zero mark ; if not, read the actual volume and calcu- late from this. Then turn the three-way tap, after having put a short rubber tube on its lateral outlet, so as to run a little water into this, and close the tube by a small piece of glass rod. As long as the tap is not used, it remains in this position. 224 THE TECHNICAL CHEMISTS' HANDBOOK Introditction of the absorbing liquids. — Draw oflf the confining liquid by means of the aspirating bottle, holding the bottom tap fast in its position, and shutting it at once when the water has got down to the capillary. Take the rubber tube off and draw the liquid back into the aspirating bottle, lest it should siphon itself off. Then pour the absorbing liquid into a small porcelain capsule, and allow it to rise in the burette. The various gases are estimated, seriatim, as follows : — 1. Carbon Bioidde, CO2, by absorption with a solution of caustic potash, 1 in 3 water — that is, specific gravity 1"23. Of thi.s 1 c.c. takes up 90-100 c.c. COj. It is sufficient, if the inside of the burette is once wetted with the solution. Afterwards water is allowed to enter from below and to run in from the top, to wash the glass ; then the normal pressure is re-established and the volume read off. In the case of crude gas the HjS must be first removed by a tube containing pumice soaked with cupric sulphate. 2. Heavy hyd/rocarbons, C„H„. — Draw out the confining water as completely as possible, rinse off the potash solution with a little water (which is also drawn off), allow about 10 c.c. of water, saturated with bromine, to enter, and shake the burette. When the space above the liquid ceases to show the brown colour of the bromine, draw off the liquid and replace it by fresh bromine water. Finally, in order to absorb the bromine vapour, draw about 1 c.c. of caustic potash solution into the burette, shake this up in the burette, allow a little water to run in at the top, establish the normal pressure, and read off the volume. Thus all the iUuminants are absorbed — i.e., ethylene and the other un- saturated hydrocarbons, also benzene vapour. 3. Oxygen is absorbed by drawing in about 2'5 c.c. of a solution of pyrogallol (1 to 5 water) and after this 7"5 c.c. caustic potash solution (1 : 3). Shake well for five minutes, run in water through the funnel until the pressure is equalised, shake again, and con- tinue this until no more water will enter the burette. Eun off the dark liquid at the bottom, allowing water to run in at the top, so that a layer of clear water remains at the top, which allows a correct reading after re-establishing the pressure. Accurate estimations of oxygen are made by titration with potassium iodide, manganous chloride, and thiosulphate, as des- cribed in Tech. Meth., vol. i., pp. 209 and 334. 4. Carbon Monoxide. — Draw off the confining water, wash with more water, draw in 10 c.c. ammoniacal solution of cuprous chloride (made by dissolving 200 g. commercial cuprous chloride and 250 ammonium chloride in 750 water, placing a copper spiral in the bottle, and before use mixing 3 vols, of this solution with 1 vol. liquor ammonise, specific gravity 0'905), shake for one minute, draw off the solution, replace it by a fresh quantity, shake again, and repeat this procedure at least twice. Alter the last removal of the absorbent, run through the funnel 3 or 4 c.c. concentrated MANUFACTURE OF COAL-GAS 225 hydrochloric acid, and then a little water, which forms a layer at the top. Draw off the liquid, wash with water, draw in 1 or 2 c.c. concentrated potash solution, shake up, allow some water to enter, re-establish the normal pressure, and take the reading. 5. Hydrogen. — The gas now contains nothing but H, CH4, and N. The hydrogen is estimated by fractional combustion, for which purpose a second burette (B) is needed. Measure in the first burette (A) 22 to 25 c.c. of the residual gas under normal pressure, and mix with air for burning the hydrogen. For this purpose open first the bottom tap, then the top tap, so as to com- municate outwards, whereupon water will run out and air enter. When the level of the water has gone down to about 5 c.c. below 0, quickly shut the top tap and after this the bottom tap, mix the gases by shaking, regulate the pressure to that of the atmosphere plus that of the column of water in the funnel, and read the volume. Now fill burette B up to the capillary and connect both three-way taps, interposing a palladium tube, C, between them. C is a tube of glass of high melting point, 10 c.c. long, 3 mm. bore, and 5 mm. thick. It contains a 100 mm. of palladium wire, 0'3 mm. thick, folded into four and introduced into the central part of tube C. By heating this part of the tube, it is made to collapse and to hold the wire fast ; the remaining portion of C is loosely filled with long fibrous asbestos. The connection between C and the capillaries of A and B is made by short, thick-walled rubber tubing. Now turn both three-way taps so that both are closed, fill the funnel of burette A with water, lower the pressure by opening the bottom tap for a moment, turn both three-way taps at the same time and quickly, so that C communicates with the interior of both burettes, and heat C. The air in C thus increases its volume, and forces the water in the capillaries back into both burettes. Now connect- the rubber tube of the pressure bottle with the lower tap of A, open this tap, heat C at its narrowed part until the smaU flame turns yellow, and open the lower tap of B, so that the gas passes from A through C into B in a moder- ately quick current. The water should issue from B in a con- tinuous jet, not in single drops, and the palladium wire should not become red-hot on the side where the gas enters ; otherwise some methane would be burnt together with the hydrogen. As soon as the water has got to the top of the burette A, quickly shut first the bottom tap of A and then that of B, and syphon the gas back from B to A as described above. After cooling, the pressure in A is made equal to the normal ; the volume is then read, and the contraction ascertained. Example : 100 c.c. coal-gas, taken for analysis, after absorbing CO2, heavy hydrocarbons, O and CO, left 85 c.c. Of this 22-2 c.c. ' were transferred to burette A, and diluted with air to 105"3. After the combustion the volume was 86"3, .showing a contraction P 226 THE TECHNICAL CHEMISTS' HANDBOOK of 19'0. Calculating this upon a 100 c.c. of the original gas, we find 19'0 X 85-0 22-2 = 72-8. 2 X 72'8 Therefore the hydrogen amounts to ^ — =48"5 per cent. o As a final control, estimate the oxygen left after combustion ; it must be less than that originally employed by two-thirds of the contraction observed. 6. Methane is estimated, together with hydrogen, by burning another portion of the gas remaining after the operations 1 to 4, in the " explosion burette." For this, measure off 12 to 15 c.c. of this gas, draw in an excess of air, shake up, ascertain the volume, draw off the confining water, explode by means of an electric spark (generated by a battery and- induction coil), ascertain the contraction, let 1 or 2 c c. potash solution run down inside the burette, and after this, slowly, some water, adjust the pressure and ascertain the total contraction, which is equal to H20-t-C02. From this deduct the amount corresponding to the hydrogen found in No. 5 ; one-third of the remaining contraction corresponds to the methane, for 1 vol. CH4+2 vols. 62=0 vols. CO2-HO vols. HgO. Example : Kesidual gas employed, 12'7 c.c. (forming part of the 86 c.c. remaining after the absorption of CO2, C„H„, O2, and CO) ; after addition of air=104'l ; therefore air employed=9r4. After the explosion remain 78"9 c.c. gas ; therefore contraction 85 X 25'5 = 25-2 ; calculated upon the total gas ^^.^ = 168-8. From this deduct the contraction due to hydrogen, according to No. 5, = 72 '8; this leaves for the methane a contraction of 168'8-72"8=96'0, or one-third of it = 32'0 per cent, methane. 7. Nitror/en is represented by the deficit from 100 after esti- mating all the other constituents. Suppose we have found : — From No. 1, 2'0 per cent, (by volume) CO „ „ 2, 4'0 „ heavy hydrocarbons » I, 3, 0-4 „ O2 „ „ 4,_8;6_ „ CO Together 15'0 „ From No. 5, 48-0 „ H2 „ „ 6,32;0^ „ CH4 95-0 „ Leaving 5'0 „ for N3 The estimation of ethylene, benzene, acetylene, naphthalene, hydrogen sulphide, total sulphur, ammonia, cyanogen, etc., is described in Lunge-Keane's Tech. Meih. of Ghem. Anal., vol. ii., pp. 659 et seq. MANUFACTURE OF COAL-GAS 227 The calorific power of coal-gas is best ascertained by means of the Junckers calorimeter, which is always sold with instruc- tions for use. B. Purifying Material (Spent Oxide). _ 1. Cyanogen (Bueb). — Boil 20 g. of an average sample of spent oxide (from which the sulphur has been previously extracted as b.elow), or the same quantity of pressed " cyanide mud," with 100 c.c. caustic potash solution (specific gravity 1"26) and 200 c.c. water for half an hour, dilute to 1010 c.c. (reckoning 10 c.c. for the volume of the solid substance), and pass through a dry filter. Take 25" c.c. of the filtrate, add 50 c.c. water and 10 c.c. dUute sulphuric acid (1 : 10), and titrate with zinc solution. This solution is made as follows : — Dissolve 10'2 g. of pure crystallised zinc sulphate (ZnS04, THjO), together with 10 c.c. sulphuric acid of specific gravity i'7 in water, make up to 1 litre, and compare this with a freshly made solution of 10 g. pure crystallised potassium f errocyanide in 1 litre, in the following manner : — To 25 c.c. of the ferrocyanide solution add 50 c.c. water and 10 c.c. dilute sulphuric acid. This mixture is titrated with the zinc solution, testing for the completion of the reaction by drops put on to filter paper (preferably Schleicher and Schiill's, No. 601, mark S) soaked with a 1 per cent, solution of ferric chloride. The end of the reaction is reached when no blue coloration is produced on the paper. Other methods for the estimation of cyanides (described by Knublauch and by Drehschmidt) are given in Tech. Meth., vol. i., pp. 546 €t seq., and vol. ii., p. 725. 2. Sulphur. — Extract 15 g. of the air-dried mass in a Soxhlet apparatus with 100 c.c. carbon disulphide in a 200 c.c. round- bottomed flask of known weight. Heat on a water-bath, con- densing the vapours by a reflux condenser, until twenty extractions have been made. Distil oflf the OSj, remove the last portions by hot air, and after cooling again weigh the flask. The difference between the weighings =S. Sometimes it is desirable to know the amount of S which on burning the oxide forms SO2, since a certain quantity of S is always retained by lime, etc., on burning the spent mass. For this purpose Pfeiffer burns 1 g. of the sample, by j)utting a piece of tinder in a litre flask filled with oxygen and previously charged with 25 or 30 c.c. of normal caustic soda solution. Finally he adds 1 c.c. neutral 30 per cent, hydrogen peroxide and titrates back with standard HCl and methyl orange. Each c.c. of the normal soda solution consumed corresponds to 1*6 per cent, of S burnt. Processes for estimating all the essential constituents of spent oxide are described in Tech. Meth., vol. ii., pp. 723 to 730. 228 THE TECHNICAL CHEMISTS' HANDBOOK Xm. OALOIUM CARBIDE AND ACETYLENE. A. — Raw Materials. (a) Coke, see p. 93. (b) Limestone, see p. 157. B. — Technical Calcium Carbide. (a) The sampling in this case has to be done with special care, since it is anything but easy to obtain a small sample representing the real average quality. The sample is quickly crushed in an iron mortar, provided with a rubber cover, or in a coffee-mill, and the powder must be kept free from contact with air. (b) The estimation of the yield of gas should always be made by actual measurement of the gas, not by loss of weight. Take 50 g. carbide, and put it into a glass tube, 2 or 3 cm. wide inside, which is connected -with the gas-generating flask (250 c.c.) by a rubber tube so that the carbide can be dropped in small quantities into the flask. 1 50 c.c. water, previously saturated with acetylene, are first placed in the flask, the cork of which is also provided with an exit-tube connected with a measuring bottle. This bottle holds 20 litres, and has a division on which J litre can be read oflF. It is connected by means of a lateral neck just over the bottom and by a rubber tube with a level-bottle of the same size, fiUed with water saturated with acetylene. By raising the level- flask, the water is forced into the measuring flask up to its neck ; during the time the gas is given off, the level-flask is lowered, so that there is never any notable pressure in the measuring bottle. When all the gas has been collected in the latter, the level-bottle is placed so that the water is exactly at the same level in both bottles, and about two hours are allowed for the temperature to reach that of the surrounding air. Read the thermometer and barometer, and reduce the volume of the gas by the tables, pp. 36 et seq., to the normal state, regarding it as saturated with moisture. If, as usual, the reduction is to be made not to 0°, but to 15° C, this can be done with sufficient accuracy by the formula : — V = ^ (140-2-0-6«)=|^ 100 ^ ' 100 where V is the volume at 15°, -y the volume at t°, and B the (corrected height) of the barometer. (Cf. Tech. Meth,, vol. ii., pp. 590 et seq.) (c) Impurities. — It is best to test for these, not in the carbide, but in the acetylene given off from it. Put 70 or 80 g. carbide, crushed to the size of a pea, into a previously weighed, well-dried, MANUFACTURE OF FERTILISERS, 229 half -litre flask, and weigh it on an ordinary balance which turns to 0"1 g. The cork of this iiask is fitted with a dropping funnel, contracted at the outlet, with glass tap, and with a side tube connected with a ten-bulb tube. Eke that shown in Fig. 8, p. 119. The latter contains 75 cm. of a 2 to 3 per cent, solution of sodium hypochlorite. Eun from the funnel three to seven drops of water on to the carbide, and shake the flask gently from time to time. The gas should all be liberated in three or four hours ; it may, if required, be measured, or else allowed to escape. Then the flask is filled up to its neck, so as to drive all the gas into the bulb- tube, and in the contents of the latter the phosphoric acid which has been formed by the h;^pochlorite from the hydrogen phosphide contained in the gas, is estimated by the ordinary magnesia method. If it is required to estimate the sulphur also, which escapes principally as H2S, divide the contents of the bulb-tube in two portions, estimate in one of these the phosphoric acid as above, and in the other the sulphuric acid, formed from the HoS, as BaSOi. XIV. EXAMINATION OF THE RAW MATERIALS AND PRODUCTS OF THE MANUFACTURE OP FERTILISERS. N.B. — This section is based on the resolutions agreed to at the Fifth International Congress of Applied Chemistry at Berlin (1903). A. — Sampling. Samples must be taken out of every tenth sack in the case of shipments in bulk, in at least ten places, by means of the samplmg-auger, described on p. 251 ; in the case of ship cargoes, from every fiftieth tub ; the total weight to be about 300 g. for each of the three normal samples. In the case of unequal composition, the samples must be ground and mixed ; in the case of moist fertilisers, this must be done by hand. B. — Moisture. Moisture in crude phosphates, bone charcoal, etc., is estimated by drying 10 g. at 100° up to constancy of weight ; in the case of gypsum, during three hours. If the substance alters its percentage of moisture during grinding, the moisture must be determined both in the coarsely crushed and in the finely ground sample, and the result of the analysis is to be calculated on the original coarsely crushed sample. 230 THE TECHNICAL CHEMISTS' HANDBOOK 0. — The Insoluble Matter. The insoluble matter is determined in 10 g. of the sample. (a) When dissolving in mineral acids, after rendering the silica insoluble by heating on the water-bath during several hours, or on the air-bath to 120°, the residue must be ignited. (6) When dissolving in water, the residue must be dried at 100° up to constancy of weight. D. — ^Phosphoric Acid. 1. Preparation of the Solutions. (a) Phosphates soluble in water. — Shake 20 g. in a litre flask with about 800 g. water for half an hour, and fiU up to the mark. Solutions of so-called double superphosphates must be boUed with addition of nitric acid (IQ c.c. concentrated nitric acid to 25 c.c. of the solution) before precipitating the i)hosphoric acid, in order to convert any pyrophosphoric acid present into orthophosphoric acid. (b) Phosphates soluble in Ammonium, Citrate are treated according to Petermann's method. In the case of super- phosphates containing upwards of 20 per cent. P2O5, take 1 g. : of those containing 12 to 20 per cent. P2O6, 2 g. ; if there is less than 10 per cent., P2O5, and, in the case of composite fertilisers, 4 g. for each sample. Grind it first dry, then with 20 to 25 c.c. water, decant on to a filter, and wash with water until the volume of the filtrate is about 200 c.c. If the filtrate is not quite clear, add a drop of nitric acid. Put the filter and residue into a 250 c.c. flask, add 100 c.c. of the ammonium citrate solution (prepared as below), digest about fifteen hours at the ordinary temperature, with frequent shaking, then one hour at 40°, allow to cool, fiU up to the mark, take 50 c.c. of the filtrate and 50 c.c. of the above aqueous solution, mix these, boil vnth 10 c.c. concentrated nitric acid for ten minutes, and estimate the total phosphoric ^.cid soluble in water and in citrate by the molybdenum or the citrate method. Preparation of the Ammonium, Citrate solution. — ^Dissolve 500 g. citric acid in water, neutralise with ammonia, allow to cool, reduce the specific gravity to 1"09, and add to a litre of this solution 50 c.c. liquor ammonise, specific gravity 0'92. The specific gravity of the final solution should be from 1"082 to 1"083. (c) Total Phosphoric Acid. — Boil 5 g. with a mixture of three parts hydrochloric acid (specific gravity 1"12), and 1 part nitric acid (specific gravity 1'20), or with 20 c.c. concentrated nitric acid and 50 c.c. concentrated sulphuric acid for half an hour, and make up to 250 c.c. (d) In Thomas-Slag Phosphates the phosphoric acid is esti- mated in the portion which passes through a 2-niillimetre sieve, but the result is calculated upon the whole sample, including the coarser portion. The following estimations are made ; — MANUFACTURE OF FERTILISERS 231 1. Phosphoric Acid soluble in Citric Add. — Shake 5 g. Thomas phosphate_ in a half -litre flask, previously charged with 5 c.o. alcohol, with a 2 per cent, solution of pure citric acid during half an hour at 17J°, in a revolving agitator which makes thirty to forty revolutions per minute. 2. Total Phosphoric Acid. — Soak 10 g. Thomas phosphate (for the analysis of fine Hour passed through sieve No. 100=0'19 mm. mesh) in a half -litre flask with 5 c.c. water, then boil with 50 c.c. concentrated sulphuric acid half an hour, stitring frequently, and fill up to the mark. 2, — Examination of the Solutions. For phosphoric acid, according to one of the following methods : — (a) Molybdenum method, according to Wagner. — To 25 or 50 c.c solution, free from silica and containing from O'l to 0'2 g. P2O5, add so much concentrated solution of ammonium nitrate (750 g. per litre) and so much molybdenum solution (150 g. ammonium molybdate, dissolved in 1 litre water and poured into 1 litre nitric acid of specific gravity 1'2) that the total liquid contains 15 per cent, ammonium nitrate, and for each O'l g. P2O5 not less than 50 c.c. molybdenum solution. Heat to 80° or 90° for ten minutes, put aside for an hour, filter, wash the precipitate with dilute solu- tion of ammonium nitrate (150 g. (NH4)NO3-1-10 c.c. nitric acid in 1 litre) until there is no reaction for calcium, pierce the filter, wash the precipitate into a beaker by means of a 2| per cent, liquor ammoniae, dissolve it by stirring, and add so much ammonia that the total volume is 75 c.c. Then add for each 0"1 g. P2O5 10 c.c. of magnesium mixture (55 g. crystallised magnesium chloride -1-70 g. ammonium chloride, dissolved in 1 litre of 2'5 per cent, liquor ammoniae), in single drops, stirring constantly, cover the beaker, allow to stand for two hours, filter the precipitate, wash it with 2'5 per cent, ammonia until the reaction for chlorine ceases, and dry at 100°. Detach the precipitate from the filter, place it in a platinum crucible, add the roUed-up filter, and carbonise it in a covered crucible ; then heat the crucible for ten minutes in an upright position over the Bunsen flame and for five minutes on the blowpipe. (b) Git/rate method. — In the case of aqueous solutions of super- phosphate, employ 50 c.c. citrate solution for 50 c.c. of the phos- phate solution, corresponding to 1 g. substance ; in that of acid solutions of bone meal, fish guano, Thomas-slag, flour, etc., take 100 c.c. of the citrate solution for 50 c.c. of the phosphate solution (=1 g. substance). The citrate solutionis, made by dissolving 1100 g. pure citric acid in water, adding 4 litres of 24 per cent, liquor ammonise, and making up to 10 litres. After adding the citrate solution, add at once 25 c.c. magnesium mixture (550 g. magnesium chloride -t- 1050 ammonium chloride, dissolved in 6| litres water 232 THE TECHNICAL CHEMISTS' HANDBOOK +3i litres 27 per cent, liquor ammonise), and shake or stir for half an hour. Filter the precipitate, preferably by means of a Gooch or Neubauer crucible (see below), rinse the beaker with 5 per cent, liquor ammonise, and wash the precipitate five or six times with the same solution, using a filter pump. Dry the crucible on a hot plate untU the mass begins to crack, ignite for three to five minutes (preferably in a Roessler furnace), and allow to cool in a desiccator. After weighing, the crucible may at once be used for a fresh determination, without removing the precipi- tate, and thus thirty or forty estimations can be made in it wifli- out renewing the asbestos filter. This method involves several errors, which, however, com- pensate one another, so that when the above details are strictly adhered to, the final result is perfectly correct. According to the - resolutions of the Union of the German Agricultural Research Stations in 1903, the citrate method' is the only one admissible for all fertilisers, except crude phosphates. The preparation of a Gooch crucible — that is, a platinum crucible with platinum sieve and asbestos filter — is a little trouble- some ; it is described in Tech. Meih., vol. i., p.'25. The Neubauer crucible (sold by W. C. .Heraeus, Hanau) is similar to the Gooch crucible, but contains a platinum sponge filter on the sieve. It is ready for use, as obtained from the dealers, and is nmch more convenient than a Gooch crucible. B. — Free Acids. (a) The total free acid is estimated by titration with caustic soda solution and methyl orange. (6) Free phosphoric acid is estimated gravimetrically in the alcoholic extract, as described above. P. — Ferric Oxide and Alumina. In Germany the accepted method is that of E. Glaser. Dis- solve 5 g. phosphate in 25 c.c. nitric acid (specific gravity 1:2) + 12-5 C.C. hydrochloric acid (specific gravity 112), and dilute to 500 c.c. Put 100 c.c. (=1 g. of the phosphate) in a 250 c.c. flask, add 25 c.c. concentrated sulphuric acid (specific gravity 1'84); after five minutes' shaking add 100 c.c. 95 per cent, alcohol, allow to cool, fill up to the mark with alcohol, shake well, and fill up again. After waiting for half an hour, filter, heat 100 c.c. of the fifirate in a platinum dish until the alcohol is driven off, transfer to a beaker, add 50 c.c. water, and heat to boiling. Remove the flame, add NH3 till the reaction is alkaline, boil ofi' the excess of NHg, allow to cool, filter, wash with hot water, ignite, and weigh. The weight found is assumed to be aluminium phosphate-)- ferric phos- phate, or 50 per cent, of it=re203-t- AUO3. MANUFACTURE OF FERTILISERS 233 Gr. — Nitrogen. 1. Nitric-nitrogen is estimated gas-volumetrically by the nitrometer (pp. 137 and 139), or by ScMoesing-Grandeau's method {Tech. Meth., vol. ii., p. 381), or by one of the methods for reducing it to NH3. The following method is due to Ulsch. Into a flat- bottomed half-litre flask put 25 c.c. of the aqueous nitrate solution (which ought to contain at most 0'5 g. KNO5=0"4 g. NaNOs) and 10 c.c. dilute sulphuric acid (1 vol. concentrated acid +2 vols, water), add 5 g. commercial "ferrum hydrogenio reductum " (iron reduced by hydrogen), and close the flask with a pear-shaped glass vessel of 25 c.c. capacity filled with water, which at the same time serves as a reflux condenser. Heat first cautiously, then more strongly, at least for half a minute to fuU boiling (altogether five minutes), dilute with 50 c.c. water, add 20 c.c. caustic soda solution (specific gravity 1'25), and distU the IsTHa formed into titrated hydrochloric or sulphuric acid. The distillation may be finished in five to seven minutes after the commencement of the boUing. By titrating back the excess of acid the quantity of NH3 is ascertained ; each c.c. normal acid saturated =0-01401 g. N or 0-06302 HNO3 or 0-10116 KNO3 or 0-08506 NaNOa. 2. Ammoniacal nitrogen, cf. p. 217. Preferably distil with freshly calcined magnesia, 3 g. to 1 g. NH3. In the case of ammoniacal superphosphates, the solution prepared as on p. 230 should be used. 3. Total nitrogen is estimated in presence of nitrates by Kjeldahl-Jodlbauer's method. Place 1 g. substance in a flask of difficultly fusible glass holding about 350 c.c, slowly add 30 c.c. phenolsulphuric acid (made by dissolving 200 g. P2O6 in 500 c.c. concentrated sulphuric acid, and 40 g. phenol in 500 c.c. con- centrated sulphuric acid, and uniting the two solutions, after cooling), shaking continuously, and cooling by placing the flask in cold water. When finished, agitate for another half -hour or hour, add a drop of mercury (about 1 g.), and then gradually 2 to 3 g. dried zinc dust, with good agitation and cooling. Allow to stand for one or two hours ; then boil until the solution has become clear and colourless, allow to cool, wash with water into a distilling flask, add 110 c.c. of caustic soda solution of specific gravity 1-285 (which must be free from nitrogen compounds), distil the NH3 into normal hydrochloric acid, and estimate it by retitrating. The calculation is made as above, svb G, 1. Dwmp substances are ground up with a little gypsum before adding the phenolsulphuric acid. 4. Organic nitrogen, in the absence of nitrates and ammonium salts, is estimated according to Kjeldahl-Wilfarth's method. Put 1 g. substance in a 150 c.c. long-necked flask of Bohemian glass, add a drop of mercury and 25 c.c. of concentrated sulphuric acid, 234 THE TECHNICAL CHEMISTS' HANDBOOK to a litre of -whicli 200 g. P2O5 and 15 g. K2SO4 have been added. Heat at first slowly, then to violent boiling, putting the flask, or several flasks, on a wire gauze in a slanting position. The whole is best placed on a sheet of lead with turned-up edges, covered with a thick layer of sand and placed under a hood, so that no damage is done if a flask is cracked. In the case of badly frothing liquids put a little paraffin in the flask and close this loosely by a Kreusler's stopper, i.e., a glass tube drawn out below into a long point, and sealed at the bottom. Continue the boiling until the contents of the flask are quite clear, which may take half an hour to three hours. Then wash its contents by the aid of 200 c.c. water into a half-litre flask, add 100 c.c. caustic soda solution of specific gravity 1"285 (free from N) and 1 to 1"5 g. zinc dust, and distil into titrated HCl, proceeding just as in No. 1. In the case of substances which cannot be finely ground, prepare a good average sample by weighing off 3 to 5 g., boU with 50 to 60 c.c. sulphuric acid and 2 to 3 g. mercury, wash, after cooling, into a 300 c.c. flask, filling this up to the mark, mix by shaking, and take 100 c.c. for the distillation with caustic soda and zinc dust. H. — Potash. Potash is estimated as in potassium chloride containing sulphate, p. 205, or by the perchloric acid method. Tech. Meth., vol. ii., p. 413. Details for the examination of the various fertilisers, ibid., pp. 418 et seq. XV. ALUMINA PREPARATIONS. A. — Raw Materials. 1. Kaolin {china clay), see p. 238, sub " Clay." 2. Bauxite (a).— Dry 2'500 g. at 100° for eight hours, boil with 30 c.c. of a mixture of 1 part concentrated sulphuric acid + 1 water, with good agitation, until vapours of SO3 begin to escape, allow to cool, run the paste slowly into 300 c.c. cold water so as to prevent heating (which would cause a precipitation of TiOj), add 10 c.c. hydrochloric acid, digest six hours with agitation, filter the solution (a) from the precipitated crude silica and make it, with the washings, up'to 500 c.c. Ignite the crude silica, weigh it, evaporate with 2 c.c. hydrofluoric acid and three drops of dilute sulphuric acid, and ignite ; the residue is weighed as AljO.,, and by deducting it from the crude silica we obtain the pure Si02. (b) Take 200 c.c. of the solution (a) ( = 1 '000 g. bauxite), neutral- ise with sodium carbonate until a slight precipitate begins to ALUMINA PREPARATIONS 235 appear, bring this again into solution by adding a few drops of dilute sulphuric acid, reduce the contained iron to the ferrous state by NaHSOs or gaseous SO2, dilute to 400 or 450 c.c, boil for two hours, replacing_ the evaporated water by an aqueous solution of SO2. The iitom'caa'ci! is thus precipitated. Allow to cool, make up to 500 c.c, pour through a dry filter and wash the Ti02 with warm water containing a little ammonium chloride, but keep the washings separate from the first filtrate. Dry, ignite, and weigh the Ti02. (c)_Boil_125 c.c. of the first filtrate obtained in (b) ( = 0"250 g. bauxite) till the SO2 has been removed, add a little zinc, dilute strongly, and estimate the iron by titration with permanganate, after having rendered the solution slightly acid by sulphuric acid, as described p. 154. (d) Alv/mina, Ferric oxide, and Titanic acid together are estimated in the first solution (a). Take 25 c.c. of this solution (=0'125 g. bauxite), add a little fuming nitric and hydrochloric acid, dilute considerably, add NHg in slight excess, boil up for a moment, filter, dissolve the precipitate again in hydrochloric acid, precipitate again with NH3 wash, filter, dry, and weigh. By add- ing the alumina found in (a), and deducting the Ti02 found in (b), and the ferric oxide in (c), we obtain the Temaindei= Alumina. (e) Ignite a fresh sample of dried bauxite for a quarter of an hour by means of the blowpipe ; the loss of weight is = chemically combined water + organic matter. B.— Control of Working Conditions. 1. The residue from decomposing the bauxite is tested by boiling 2 g. with 3 c.c. concentrated sulphuric acid +3 c.c. water until the red colour is destroyed, diluting a little, filtering, and making the filtrate up to 100 c.c. In this we estimate : (a) Iron in 10 c.c. by reducing it to the ferrous state and titrating with KMn04, p. 154. (b) Ferric oxide + Alumina by precipitation with NH3. (c) Soluble soda by boiling 20 c.c. with a solution of ammonium chloride and absorbing the NH3 set free in titrated hydrochloric acid. 2. Aluminate solution. — In this we estimate NajO and AI3O3 in the same operation, as described below for sodium aluminate. C. — Commercial Products. 1. Sulphate of Alumina and Alum : — (a) Estimation of Alumina — {a.) Gravimetric estimation. — Dis- solve 10 g. in water, dilute to i litre, take 50 c.c. of the clear solu- tion =1 g. of the substance, add ammonia in slight excess, boil up for a moment, filter, wash, dry the precipitate, ignite, and weigh the AI2O3. It is slightly contaminated with traces of iron, silicate, and phosphoric acid, which may be neglected. 236 THE TECHNICAL CHEMISTS' HANDBOOK (^) Volumetric Analysis. — Dissolve 5 g. in water, dilute to ^ litre, take out 50 c.c.=0"5 g. substance, neutralise the free acid by dilute solution of caustic soda (indicator : methyl orange, till the pink changes to yellow), then add phenolphthalein, and titrate with standard caustic soda solution until the red colour appears. Each c.c. of the NaOH solution corresponds to O'l'ZOS g. AI2O3. Jf.B. — This method gives only approximate results, unless a number of precautions, detailed in Tech. Meth., vol. i., p. 613, are observed. (b) Iron cannot be estimated either gravimetrically or by titration, on account of its small quantity. Hence it is estimated colorimetrically by Lunge and Keler's method. We require for this a number of small stoppered cylinders of white glass, 13 mm. internal diameter, 17 cm. high, containing 25 c.c. divided in 0"1 c.c, and a free space of 5 c.c. above the 25 c.c. mark. Also the following reagents : — (1) a 10 per cent, solution of potassium thiocyanate ; (2) pure ether ; (3) a solution of 8'630 g. ammonium-iron-alum and 5 c.c. concentrated sulphuric acid in 1 litre; (4) a solution prepared from (3) by diluting it in the proportion of 1 : 100, so that this solution contains 10 mg. Fe per litre. It should be kept protected from sunlight, but even then keeps only for a few days, whereas solution (3), when pro- tected from air and light, keeps a long time without getting turbid ; (5) pure nitric acid. It is hardly possible to obtain nitric acid absolutely free from iron, but this does not matter, if it gives only a slight pink colour with potassium thiocyanate, since very little of it is used, and an equal quantity for the check test as for the actual test. 1 Dissolve 1 or 2 g. of the aluminium sulphate,_ weighed. exactly, in a little water, add exactly 1 c.c. of the pure nitric acid (5), heat a few minutes, allow to cool, and dilute to 50 c.c. Put 5 c.c. of this solution into one of the colorimeter cylinders, A. {N.B. — If this method is applied to estimate traces of iron in sulphuric acid, this is diluted in the same way.) Into a second cylinder, B, put 5 c.c. of dilute nitric acid, obtained by diluting 1 c.c. of (5) to 50 c.c, and a certain accurately measured quantity of the iron- alum solution (3), e.g., 1 c.c. Add as much pure water to cylinder A as you put iron solution in B, so as to always have the same degree of dilution in A and B. Then add to both A and B 5 c.c. of the thiocyanate solution (1) and 10 c.c. of the ether (2), put the stopper in and shake thoroughly, until the aqueous layer has become colourless and the red colour has passed over entirely into the ether. The comparison of the colours in A and B is most accurate after a few hours, since they deepen a little on standing, but marked differences can be observed at once, so that three cylinders will suffice_, of which A receives the solution to be tested, B and C the quantities of iron most nearly approach- ing to A. The comparison is made by holding the cylinders a little ALUMINA PREPARATIONS 237 distance from a white surface {not putting them down upon it !) and looking at them from the top downwards. It is then quite easy to estimate differences of ± 0"1 c.c. of the iron-alum solution (5), that is of ± O'OOl mg. Fe in the 5 c.c. employed for analysis, but only when the total quantity of iron does not exceed 2 c.c. of the solution, that is=0"02 mg. Fe. If there should be more than this present, the permanganate method, p. 112, is appli- cable. (c) Free acid in aluminium sulphate cannot be directly titrated by any of the hitherto known indicators. Beilstein and Grosse proceed as follows : — Dissolve 1 or 2 g. of the sulphate in 5 c.c. water, add 5 c.c. of a cold saturated solution of ammonium sulphate, stir fifteen minutes, and precipitate with 50 c.c. 95 per cent, alcohol. Wash the precipitate with 50 c.c. alcohol, evaporate the alcohol from the mixed filtrate and washings on the water- bath, and titrate the acid in the residue by decinormal soda solution and phenolphthalein. (d) Zinc only occurs occasionally in commercial sulphate of alumina, but is very injurious. Estimate it by adding to the solution of the sulphate a sufficient quantity of barium acetate to precipitate all the sulphuric acid, and precipitating the zinc in the filtrate as ZnS. 2. Aluminate of Soda : — (a) Soda and Alumina. — Dissolve 2 g. in water, dilute to 100 c.c. and titrate 10 c.c. (=0"2 g. substance) quite hot, with phenolphthalein as indicator, by fifth normal hydrochloric acid until the red colour has vanished. The soda only is saturated at this stage, and each c.c. of the acid corresponds to 0'0062 g. NaaO. Now add a single drop of methyl orange and continue the titration with the same acid, but at a temperature of 30°, until the alumina first precipitated has been redissolved and the red colour has appeared. Each c.c. of acid used in this second titra- tion corresponds to 0'003407 g. AI2O3. The percentage is obtained directly when employing 0'200 g. substance by multiplying the c.c. used in the first titration (a) by 3'105=per cent. NajO, and those used in the second titration (b) by l'704=per cent. AI2O3. (b) Insoluble matter is estimated in 10 to 20 g. substance in the usual manner, but employing "hardened" filtering paper, since ordinary filter paper would not stand the strongly caustic solution. (c) Silica is estimated by evaporating with hydrochloric acid, digesting the residue with dilute HCl, filtering, washing, igniting, and weighing the residue. 3. Commercial Alumina is either the hydrate or anhydrous. In this the silica occurring as an impurity is estimated as in 2 (c) ; total soda by igniting at a red heat, digesting with water, heating with normal HCl, and titrating back the excess of acid ; soluble soda by boiling with 100 c.c. water and titration with normal HCl and phenolphthalein ; iron in the hydrochloric acid solution as in 238 THE TECHNICAL CHEMISTS' HANDBOOK No. 1 (b); loss of weight on ignition ( = H20 + C02) by heating for fifteen minutes over the blowpipe. XVI. CEMENT INDUSTRY. A. — Portland Cement. 1. Ra-w Materials. (a) Limestone. — (a) Estimate carbon dioxide, as described p. 158, by titration or by volumetric estimation of CO2, p. IVl. It is calculated as CO2. In the presence of considerable quantities of magnesia' (which is considered as an injurious constituent of cement), estimate it in the hydrochloric acid solution, as on p. 148, calculate it as MgCOs, and calculate the excess of CO2 as CaOOa. (p) Argillaceous residue is the difference between 100 and the carbonates found in (a). If there is much present, it may be examined like clay, No. (b). (b) Clay. — The percentage of coarse samd (quartz) is found by elutriation. Weigh 50 g. of the coarsely ground, dried average sample into a rather large porcelaia dish, pour over it 100 c.c. dilute hydrochloric acid (1 concentrated acid + 8 water), boil for about three hours, allow to cool, pour off the acid and direct a jet of water on to the mass, carefully rubbing it up with the fingers, so that only clay goes away with the water and pure sand remains behind. This plan is better than the application of mechanical elutriating apparatus. The sand may be sorted by sieves into different sizes, viz., fine dust (down to 0"025 mm.), dust (0'040 mm.), fine sand (0'20 mm.), coarse sand (above this). Complete analysis of clay (cf . Tech. Meth., vol. i., pp. 569 et seq., and pp. 688 et seq.). 1. Decomposition by m,eans of alkaline ca/rbonate, i.e., a mixture of equal parts potassium carbonate and sodium carbonate, of which 6 to 10 g. are required for one part of clay. Dry the clay at 120°, grind it very finely, mix it intimately with the alkaline carbonate in the platinum crucible itself by means of a platinum or glass spatula (which is afterwards cleaned with a little car- bonate)^ and heat in the covered crucible, first slowly, then up to full, quiet fusion. A good Bunsen or Fletcher burner is prefer- able to the blowpipe for the heating. After cooling, heat the bottom of the crucible by a small flame to a low red heat twice succes- sively, in order to facilitate the separation of the fused mass, allow to cool, pour a few c.c. of water, and heat gently with a small flame, until the cake detaches itself from the crucible. Wash it into a good-sized platinum dish, cover this with a large watch-glass and heat on the water-bath until the mass has softened and fallen CEMENT INDUSTRY 239 to powder. Then add an excess of hydrocUoric acid, remove the watch-glass, wash its under-surface, and evaporate to dryness on the water-bath. During the evaporation the mass is stirred with a flass rod, so as to render the residue powdery. Then heat the ish in an air-bath to 120' for an hour, moisten it, after cooling, with moderately strong hydrochloric acid, allow to stand for an hour, heat up with water, pour the clear portion through a filter, and continue this treatment until the residue ceases to yield a colour with hydrochloric acid. Then transfer it to a filter, wash, dry^ and ignite it first over a small flame, then to constancy of weight, and weigh it as silica. It may still contain some titanic acid. This is separated by evaporating with hydrofluoric acid and concentrated sulphuric acid on the water-bath as a residue which should be tested whether it yields the purple microcosmic salt bead ofTiOa The filtrate from the titanic acid is divided in two halves. In one of these estimate alumina + ferric oxide by adding pure liquor ammonise (free from carbonate) in slight excess, boUing up for a moment, filtering, washing, and igniting. In the other half estimate the iron by reducing with zinc and titrating with per- manganate, c/. p. 112. In the filtrate from the precipitate of AI2O3-I-F2O3, estimate calcium by precipitation with ammonium oxalate (p. 148), and in the filtrate from this magnesium by ammonium phosphate (p. 148). 2. 2^he Alkalies can be estimated, if desired, by decomposing about 5 g. clay with hydrofluoric acid ; of. Meth. Tech., vol. i., p. 694. 3. Sulphur, present as sulphates or pyrites, is estimated by oxidation with aqua regia and precipitatmg the hydrochloric acid solution with barium chloride ; cf. p. 108. 4. Carbon dioxide, as in the case of limestone, pp. 158 or 171. 5. Loss of weight on ignition over the blowpipe or a powerful gas burner gives water -h organic matter 4- C02-t- sulphur present as pyrites, etc. (c) Separation of silica present as quartz, and that present in the form of silicates. — The separation of these two kinds of silica is frequently demanded in so-called "rational analysis of clay." It can be eflfected by the process of Lunge and MUberg (^Z. angew. Chem., 1897, p. 393), on the basis of the observation that extremely finely divided quartz is dissolved by concentrated caustic soda solution, but not by a 5 per cent solution of sodium carbonate, whilst the latter dissolves the siHca, separated from silicates by strong acids in an amorphous state, when heated on the water-bath for half an hour. This is applied to the separation of the two modifications of silica as follows : — Heat 5 g. of clay (dried at 120°) with dilute sulphuric acid (50 c.c. concentrated acid -t- 100 c.c. water) to boiling in a porcelain or platinum dish, covered with a watch-glass, until the water has been driven off and fumes of SO3 begin to escape, allow to cool, dilute with water. 240 THE TECHNICAL CHEMISTS' HANDBOOK pour off the liquid, moisten the residue with hydrochloric acid, neat for a quarter of an houi, filter, and wash. Wash the moist residue, which contains a mixture of both modifications of Si02, into a porcelaia dish, make up the solution to about 250 c.c, add about 12'5 g. pure anhydrous sodium carbonate, and heat on the water-bath for haK an hour. Then pour off the clear liquid and repeat the treatment with 5 per cent, solution of ]Sra2C03 three times. Finally, wash the insoluble matter on to a filter and wash it thoroughly with water containing a little alcohol. The dried and ignited residue consists of the SiOa present as quartz ; the difference between this and the total SiOj found in (b) 1 is the Si02 present as silicates. 2. Control of the Working CcAiditions. The crude mixture is tested for its percentage of clay and calcium carbonate like limestone ; compare A, 1. Usually the estimation of CO2 (pp. 158 or 171) is sufficient. The clinker is analysed like the finished cement, if this is required. 3. Commercial Cement. Ignite 1 g. cement in a platinum crucible over the blowpipe for fifteen minutes, decompose by hydrochloric acid, filter from the insoluble matter, fuse this with sodium carbonate, dissolve the melt in water, and unite this solution with the filtrate previously obtained. In this solution the following estimations are made : — (a) Silica is determined by boiling down the united solutions and filtering off the precipitated SiOj. The filtrate is again concen- trated by boiling, and any Si02 that separates is united with the first portion. Dry the total (crude) sihca, heat on the blowpipe for half an hour, and weigh. Then heat with 10 c.c. hydrofluoric acid and four drops concentrated sulphuric acid tUl fumes cease to be given off, and deduct the residue from the crude Si02 ; the portion thus removed by volatilisation represents the real SiOj. (b) Divide the united filtrates into two halves. In one of these estimate the Sesquioocides, Al^Os-t-FejOs, by precipitation with pure liquor ammoniae, as on p. 239. (c) Ferric oxide is estimated in the second half of the filtrate from (a), by reducing to the ferrous state by means of zinc or H2S and titrating with permanganate ; cf. p. 112. (d) Calcium is estimated in the filtrate obtained in (b) by precipitation with ammonium oxalate, p. 148. (e) Magnesium in the filtrate from (d), by precipitation with ammonium phosphate, p. 148. (f ) Sulphates are determined in a special sample by dissolving 1 g. in hot hydrochloric acid, filtering, and precipitating with barium chloride, p. 108. (g) Total sulphur. — Fuse 1 g. cement with sodium carbonate PREPARATION OF STANDARD SOLUTIONS 241 and a little potassium nitrate, dissolve in liot water, filter, acidify, and precipitate with barium chloride. (h) The estimation of alkalies is rather troublesome, and is only carried out in exceptional cases ; cf . Tech. Meth., i., p. 694. (i) The physical tests for fineness of grinding, time of setting, breaking strain, etc., are described ibid. B. — Hydraulic Lime and Roman Cement. The raw material for these are marls. In these usually only CO2 and argillaceous residue are estimated, as in the case of hme- stone, p. 238. An accurate analysis can be made as described for clay, p. 238, more especially the separation of the silica present as quartz from that of the silicates. C. — Fuzzuolanas, Trass^ Granulated Blast- Furnace Slag. 1. Hygroscopic water is estimated by drying 10 g. at 110.° 2. Chemically combined water. — Ignite 1 g. of the substance dried as in No. 1 in a platinum crucible by means of the blowpipe, a Hempel gas-furnace, or other suitable means. The tempera- ture ought to be raised gradually, so as to attain a red heat in about ten minutes, in order to avoid mechanical losses by dust being carried away through a. sudden liberation of steam. After this continue the heating for half an hour to a yellow heat, and then transfer at once to the desiccator. The loss of weight is an important criterion for the hydraulicity. 3. Silica present as silicates should be estimated as well as that of quartz as an important hydrauhc factor, as described p. 239. 4. Mechanical tests for fineness of grinding, etc., as for cement, supra, p. 238. XVII. PREPARATION OP STANDARD SOLUTIONS. Introduction. The analytical methods given in the foregoing pages are based upon the metric system of weights and measures. As there are still some laboratories in which the English system is used, the following remarks on the relation of the metric to the English system may prove useful. The unit of weight of the English system is the grain. All normal solutions are prepared so that 1000 grains by volume (100 decems) contain one equivalent of the reagent in grains, and con- sequently all normal solutions prepared on the English system are identical in concentration with those prepared on the metric system. Q 242 THE TECHNICAL CHEMISTS' HANDBOOK English, burettes usually hold 1000 grains, and are divided into 100 parts of 10 grains each, called one decern. The decern corre- sponds to the cubic centimetre. As, however, this unit, the decern, is ten times the unit of weight, the following rules must be observed when any of the data are to be changed from the metric to the English system : — Instead of Litre read 10,000 grains. ,, Cubic centimetre read decern, or ten times the number of grains. „ Grams read ten times the number of grains. If, for instance, we are told to prepare a standard solution of permanganate by dissolving 15"820 g. of potassium permanganate m 1 litre of water, and that 1 c.c. of such a solution corresponds to 0'028 g. of iron, we shall obtain a solution of equal strength by dissolving 158"20 grains in 10,000 grains of water, and 1 decern of this solution will correspond to 0"28 grain of metallic iron. No errors can possibly occur if the reader will always substitute ten times as many grams for any number of grams, ten times as many grains, or an equal number of decerns, for any number of cubic centimetres, and 10,000 grains for every litre. Where we are directed to measure out by means of a pipette 50 c.c, we take 500 grains instead, etc. ; but when speaking of the number of cubic centimetres on the burette, we substitute exactly the same number of decerns. It will also be useful to remember that : Grams per litre = grains per 1000 grains. „ „ = ounces per 1000 ounces. „ „ = ounces per cubic foot (approxi- mately). Grams per litre -;- 16 = lbs. per cubic foot. Grams per litre x 70 = grains per 70,000 grains. » ,) „ = grains per gallon. 0'4375 X grams per cub. metre = grains per cubic foot. Kilograms per cubic metre = lbs. per 1000 lbs. „ „ „ = lbs. per 16 feet. Kilograms per cubic metre ,, ^. „ ^ 5 *-r-^ = lbs. per cubic root. 16 X cub. metres per kilogram = cubic feet per lb. Kilograms per square metre = 0'205 lb. per square foot Kilograms per sq. metre x 4'8d = lbs. per square foot A. — Normal Acid and Alkali. As basis of Alkalimetry and Acidimetry, we employ chemically pure sodium carbonate. This is tested for purity by dissolving 5 g. in water, which ought to yield a perfectly clear, colourless solution; if, after acidifying this solution with PREPARATION OF STANDARD SOLUTIONS 243 nitric acid, no opalesoence is caused by barium chloride, or silver nitrate, the salt may be taken as sufficiently pure. Before using it, the sodium carbonate must be heated in a platinum crucible, which is half -filled with it and is placed on a sand-bath, the sand reaching to the same level outside as the carbonate inside. A thermometer is put in, which at the same time serves as a stirrer. The temperature is raised to 270° to 300° for about half an hour ; the contents are then emptied hot into a stoppered weighing- bottle, which is kept in a desiccator up to the time of weighing. Then weigh off, for normal acid, four portions of about 2 g. each into the beakers in which the titration is to take place ; for one- fifth normal acid the single portions ought not to exceed 0"4 g. The balance ought to turn to at least 0'5 mg. As normal acid we prefer hyckochloric acid,_ which has the following advantages over sulphuric and oxalic acid, viz. : — 1st, It is more generally applicable, e.g., for alkaline earths ; Snd, its strength, after being fixed by pure sodium carbonate, can be most accurately checked by silver nitrate, far more accurately than that of sulphuric acid by barium chloride ; 3rd, it does not change on keeping, like oxalic acid. Normal HCl (36"47 g. HCl per litre) is prepared as follows : — • Dilute pure hydrochloric acid to 1"020 specific gravity (4° Tw.). Such an acid will be rather too strong. Fill a burette with this acid, and titrate with it one of the weighed samples of sodium carbonate, the weight of which is w grams. Suppose that x c.c. of this acid are required. As the acid is sure to be too strong, x will always be smaller than "' , and we shall have to add to ■^ 0-053 every ic c.c. of the acid ^ x c.c. of water, and if the total ■^ 0-053 quantity of acid of specific gravity 1-020 amounts to V c.c, the amount of water to be added thereto to render it correct will be n c.c, where to = V ( — — — - 1 )• For one-fifth normal acid ' \ 0-053 X J the above factor would be = . If accurate normal alkali is at hand, it may be similarly employed for examining the provisional acid, and then adjusting it to the normal strength. In any case, the mixed normal acid must be checked by titrat- ing new samples of sodium carbonate, when x ought to = -— — — A further check is afforded by estimating the chlorine gravimetri- cally by silver nitrate; 10 c.c. (=0-3647 HCl) ought to yield 1-4334 g: AgCl. The ordinary indicator in alkalimetry and acidimetry used to be tincture of litmus, which must be kept in open vessels, to avoid 244 THE TECHNICAL CHEMISTS' HANDBOOK its being spoiled. When employing litmus, the liquid to be tested must be kept boiling for some time, in order to expel aU CO2, and normal acid must be added as long as, on further boiling, the colour changes back from red to purple, or blue. This prolonged boiling causes some alkali to be dissolved from most kinds of glass, which makes the tests inaccurate. A test with litmus rarely lasts less than half an hour, usually more. Phenolphtha- lein has exactly the same drawbacks. Even the action of the carbon dioxide contained in the air, which comes into contact with the Kquid on cooling, may cause trouble in very accurate work. On the other hand, a test is finished in a few minutes, if litmus is replaced by a very dilute solution of methyl orange (dimethylammoazobenzene-sulphonic acid), but in this case the liquids miist not be hot, but at the ordinary temperature, and only mineral acids, not oxalic acid, may be employed. The cold solution of sodium carbonate is coloured just perceptibly yellow by adding a drop or two of the solution of methyl orange, prefer- ably by means of a pipette ; if the colour is too intense, it will cause the transition into red on neutralisation to be less sharp. CO2 does not act in the least upon methyl orange ; a change of colour only takes place when all NagCOj has been decomposed.' When the NajCOa has been exactly converted into NaCl, the colour turns from yellow to brownish, which is due to the action of free CO2 on the indicator. At this point the reading is made, preferably by means of a Gockel screen. Just one drop of acid is then added, when the colour ought now to become distinctly pink. If it remains brownish, another drop of acid is added, and so forth. Exactly the same course is followed in titrating acids with caustic soda solution; in this case also the reading is taken at the brownish transition colour, before the change to yellow has taken place. The results obtained in this way are identical with those obtained by the proper appHcation of litmus or phenolphthalein, that is, working with these indicators under complete exclusion of air, with prolonged boiling, and in porcelain or silver vessels. The great advantage of methyl orange over the last-named indicators is the saving of time, the workmg at ordi- nary temperatures, and the possibility of employing glass vessels without any danger of error caused by the use of tMs material. Another advantage of methyl orange is that it is not affected by sulphuretted hydrogen (which destroys litmus) ; hence it can be employed, e.g., for the direct titration of black-ash liquors. Sidphur dioodde acts upon it like the stronger mineral acids, but only to the extent of one-half of its equivalent ; that is, the point of neutrality is reached when the compound NaHSOs has been formed. In the presence of nitrous acid methyl orange is gradu- ally destroyed, but it is quite easy to employ it even in this case by proceeding as described on p. 135. The above description of the transition from yellow through PREPARATION OF STANDARD SOLUTIONS 245 brownisli to pink applies only to more accurate work, e.g., when employing fifth-normal acid and alkali. With normal or semi- normal liquids this intermediate colour is hardly observed, the change passing directly from yellow to pink, and vice versa. It is generally agreed that methyl orange is the best indicator for titrating bases by means of strong mineral acids, and this holds good also for the titration of the strong acids — sulphuric, hydrochloric, and nitric acid. In these cases, indeed, its advantage over litmus or phenolphthalein is even more marked, because a slight percentage of CO2 in the standard alkali employed has no effect. But organic acids cannot be titrated with methyl orange. Some authors have proposed, in lieu of methyl orange, the unsiilphonated compound, dimethylaminoazobenzene, but this is only soluble in alcohol, and cannot bj recommended. This is also the case with ethyl orange. To prepare standard alJcali, dissolve about 50 g. of the best commercial caustic soda in 1 litre of pure water and titrate 50 c.c. of this solution with standard acid. More than 50 c.c. of acid will be required; we call this x c.c. The fraction shows the number of c.c. of the first solution, which must be diluted with pure water to 1 litre in order to obtain a really normal alkali. The solution thus prepared is again checked by titration with normal acid. The normal alkali, when intended to be used with litmus, should be as free as possible from carbonate, and should be protected against absorption of CO2 from the air, because other- wise the change of colour does not take place suflBciently rapidly, and markedly in cold solutions. A solution of sodium hydroxide entirely free from carbonate is difficult to prepare and to preserve when in constant use. When employing methyl orange as an indicator, an ordinary caustic soda solution may be employed without any special precautions. The caustic soda employed should not contain more than a very small proportion of alumina ; ordinary strong caustic nearly always fulfils this condition, or it may even be replaced by a solution of 53"00 g. pure sodium carbonate in 1 litre water, which is employed cold, and which yields as accurate results as NaOH, no notice being taken of the CO2 which escapes with effervescence. The general use of this solution is, however, inconvenient on account of the efflorescence on the burettes, necks of bottles, etc. Weaker {e.g., fifth-normal, or even seminormal) solutions do not have this drawback. All standard solutions must be prepared and employed as nearly as possible at a certain temperature. Mohr prescribes 15° ; some prefer 18° C, as being more suitable for laboratories. When the solutions have stood for some time in bottles, a little water is evaporated and recondensed in the upper part of the bottles ; the contents must then be properly mixed by shaking. 246 THE TECHNICAL CHEMISTS' HANDBOOK If the.temperature of the laboratory differs more than 2° or 3° from that employed for preparing the standard solutions, a correc- tion should be made by means of the following table. In order to reduce the volumes read off at t° to 15°, deduct per 100 c.c. the following amounts : — f c.c. t° c.c. 15 23 0-135 16 0-013 24 0-156 17 0-027 25 0-179 18 0-043 26 0-202 19 0-059 27 0-227 20 0-076 28 0-252 21 0-095 29 0-278 22 0-114 30 0-305 B. — Potassium Permanganate. The ordinary solution is seminormal, i.e. it yields 0"004 g. oxygen per c.c. It serves, e.g., for estimating nitrous acid in sulphuric acid, for testing the nitrogen acids in the chamber exits, for testing manganese ore, for testing Weldon mud, etc. Since iron only occurs in very small quantity in the products of alkali manufacture, it is best estimated by means of a tenth or twentieth normal solution made from the seminormal solution by dilution, and corresponding to 0-005584 or 0-002792 g. Fe per c.c. respectively. The solution is made by dissolving pure crystallised potassium permanganate, and is then quite stable, if protected from dust and direct sunlight. With perfectly pure KMn04, and with absolutely pure water, it would be necessary to dissolve 15-803 g. per litre. Since, however, there is no certainty of the absolute purity either of the salt or of the distilled water, we dissolve 16 g. of well-crystallised permanganate in 1 litre of distUled water, and allow to stand for a week before standardising it, so that the KMn04 may complete its action upon the impurities contained in the water. Only then is the titre of the solution checked as below, and eventually brought to exactly seminormal by adding a little water. Prepared in this manner, and protected against dust and direct sunlight, the solution keeps for any length of time. None of the methods formerly employed for standardising permanganate (by means of metallic iron, or oxalic acid, or hydrogen peroxide, etc.), is entirely free from objections. No such objection exists to the employment of Kahlbaum's pure sodium oxalate, first proposed by Sorensen. This salt need only be kept for a few hours in a drying oven at 100°, and then allowed to cool in a desiccator over calcium chloride. Dissolve about 1-3 g. of this (exactly weighed) in about 200 c.c. water, heated to 60° to 70°, add dilute sulphuric acid, and run in the permanganate solution from a burette, first quickly, then drop by drop, until PREPARATION OF STANDARD SOLUTIONS 247 a permanent red colour is produced. If a be the weight of sodium oxalate, 6 the c.c. of permanganate solution used, the fraction = gives the quantity of oxygen given off per c.c. of the permanganate solution. If a brown precipitate (of MnOa) should be formed during the titration, the experiment must be rejected, but this occurs only when the solutions are too concentrated or too hot (i.e. above 70°). Special rules for standardising permanganate solutions by means of sodium oxalate are given by Me. Bride in J. Soc. Chem. Ind., 1913, p. 1131. Permanganate is best employed in a burette with a lateral hollow glass-tap. Any change in its titre (due to dust, etc.) is perceptible by a deposition of Mn02 in the bottle. It is advisable to check the solution once every three months. Permanganate can be used with perfect accuracy in the presence of free hydrochloric acid, if the solutions contain a con- siderable quantity of manganese salts ; in other cases the same effect is produced by adding, say 1 g. of manganese sulphate free from iron. 0. — Iodine Solution. Weigh exactly 12"692 g. of pure resublimed iodine (either bought as such, or prepared by grinding up commercial iodine with 10 per cent, of potassium iodide and resubliming) on a balance turning at least with 5 mg. ; put it into a litre flask con- taining a concentrated solution of 15 to 18 g. KI, close the flask, agitate till the iodine is completely dissolved, and fill up to the mark. This decinormal solution is checked by the arsenite solution (p. 248). Both solutions ought to be precisely equivalent, c.c. per c.c. For estimating very small quantities of sodium sulphide a special iodine solution is sometimes made, by dissolving 3'2515 g. of pure iodine with 5 g. of potassium iodide in a litre, to correspond to 0"001 g. NajS per c.c. Solutions of iodine, especially the more dilute ones, keep a long time in well-stoppered bottles in a cool place, but they ought to be checked once a month by the arsenite solution. Preparation of the starch solution. — Grind up 3 g. potato starch with a little water to a homogeneous paste ; introduce this gradually into 300 g. of boiling water, contained in a porcelain dish, and continue the boiling till an almost clear liquid has been produced. Allow this to settle in a tall beaker, pour the clear portion through a filter, and saturate^ it with common salt. This solution, when kept in a cool place, is stable for some time ; as soon as fungoid growths are noticed in it, it is thrown away. A very convenient form of soluble starch is that made by Zulkowsky's method, by heating 100 parts of concentrated glycerine with 6 parts of starch to 190° C. for about an hour. 248 THE TECHNICAL CHEMISTS' HANDBOOK pouring into water, precipitating the soluble starch by alcohol, and filtering. This starch is kept in the state of a thick paste, not to be aflowed to dry, and a small quantity is taken out for each test by means of a glass rod. There are also other forms of soluble starch, e.g., " ozone-starch.'' D. — Sodium Arsenite Solution. This serves for standardising the iodine solution, and as its volumetrical complement, especially in testing bleaching powder. Employ commercial pure powdered arsenious acid ; test its purity by subliming a little from a smaU dish into a watch-glass, when no yeUow sublimate of AS2S3 (which volatilises more easily than AS2O3) should result initially ; on heating more strongly it should leave no residue. Before use the powdered As203is kept for some time over sulphuric acid in a desiccator, and can then be weighed out without any special precautions, since it is not- hygroscopic. For preparing a decinormal solution, weigh out exactly 4'948 g. AS2O3, dissol^ie it in a little hot solution of caustic soda, neutralise with dUute sulphuric acid (using phenolphthalein as indicator); add a solution of about 20 g. sodium bicarbonate in 500 c.c. water, and dilute on cooling to 1000 c.c. This solution is quite stable, and equivalent to 0'003546 g. chlorine or 0'012692 g. iodine per c.c. If really pure and dry arsenious acid has been employed, the above solution will be correct at once. But when preparing large quantities, it ought to be checked by grinding up 0"5 g. iodine with O'l g. potassium iodide, heating this mixture in a small dish on a sand-bath or upon an asbestos board till abundant vapours arise, covering with a dry watch-glass, allowing the major portion, but not the whole, of the iodine to sublime into the watch-glass, covering this with a second watch-glass which fits air-tight upon the former, and has been weighed with it, and weighing. Slip the watch-glasses into a solution of 1 g. of potassium iodide (free from iodate), in 10 g. water, wait a little till the iodine is dis- solved, dilute with 100 c.c. water, and titrate with the arsenite solution. When the colour is only a light yellow, add a little starch solution, and titrate exactly till the blue colour has just vanished. The c.c. of arsenite solution used, multiplied by 0'012692, ought to correspond exactly with the weight of iodine taken. Or the dry, sublimed iodine is transferred directly from the upper watch-glass into a tared stoppered weighing-bottle, weighed, and dissolved in KI solution in the same bottle. B. — Silver Solution. Weigh out exactly 16"989 g. of pure crystallised silver nitrate, preferably kept in a desiccator for a few hours, and dissolve in 1 litre. This gives a decinormal solution, corresponding per c.c. to RULES FOR SAMPLING 249 0-003546 g. CI, or 0-003647 g. HCl, or 0-005846 g. NaCl. By dis- solving 2-906 g. AgNOs in 1 litre, a solution is obtained corre- sponding to 0-001 g. NaCl per c.c. Ammoniacal silver solution, for Lestelle's estimation of alkaline sulphides, is obtained by dissolving 13-818 g. of pure silver in pure nitric acid, adding 250 c.c. liquor ammonise, and diluting to 1 litre. Each c.c. of this corresponds to 0-005 g. NajB. P. — Copper Solution. Copper solution, for testing ferrocyanide, is obtained by dis- solving 12-486 g. pure crystallised, not eiBoresced, cupric sulphate, in 1 litre water. {Gf. p. 170.) G. — Oxalic Acid Solution. Oxalic acid solution is employed for testing the "base" of Weldon mud, and caustic soda or lime in the presence of carbonate (pp. 157 and 158). Dissolve 63-03 g. pure, not effloresced, crystal- lised oxalic acid in 1 litre water, and check with normal alkali. This solution is not quite stable, especially when exposed to day- light ; nor can it be employed for alkalimetry, when using methyl orange as an indicator. XVm. RULES FOR SAMPLING. A. — Fuel.* Take a shovelful of each wheelbarrow, basket, etc., throw it into a cask or tub closed by a lid, coarsely grind up the whole without delay, mix the contents, spread them out in a flat, square heap, divide this diagonally into four quadrants, remove two opposite quadrants, grind up the other two more finely and mix them again, and continue in this manner untU the weight has been reduced to about J cwt. Put this into a tin box, which is soldered up and sent to the testing-laboratory. There this sample is ground again, mixed up, and divided into twelve or sixteen portions in the manner of a chess-board. Take out a teaspoonful from each of these portions and grind them in a porcelain mortar to a powder as fine as dust. This powder is kept in a stoppered bottle, and is well mixed up before taking out a fresh sample for testing. For separate moisture tests, a number of samples are taken during the first sampling, and kept in air-tight vessels. B. — Ores and Minerals (Pyrites, Manganese, Salt, etc.) (a) Smalls, slack, salt, or other substances not requiring to be crushed. — Take a sample of about 1 lb. of each weighing-tub, cart, * According to the rules laid down for the German Official testa of steam-fioilers and steam-engines. 250 THE TECHNICAL CHEMISTS' HANDBOOK or the like, by means of a scoop, so as to obtain about the same quantity each time. Of railway trucks, which are tipped directly into the warehouse, take three samples, one from the middle and one from each end.* AU these single samples are put in a cask and kept covered, to prevent the evaporation of moisture. When the large. sample is taken, empty the contents of the cask on a level, clean, and hard place, spread it flat, heap it up in a cone at the centre by going regularly round with a spade ; spread this heap again ilat, and take a sample of about a quarter of the mass, by taking out with a spade two strips crossing each other at right angles, and adding a little from the centre of each remaining quadrant. Treat this reduced sample exactly like the larger one, so that a third sample of about 5 lbs. is obtained. Mix this again thoroughly, and fill it into four (or more) wide-necked bottles of 4 ounces capacity, placed close together on a sheet of paper, so that a portion of each handful gets into each of the four bottles. When these are full, they are at once closed with tight-fitting corks ; these are cut off straight above the necks of the bottles and well covered with sealing wax, putting on the seals of both buyer and seller, or any other party concerned. The mixing and filling must be done as quickly as possible, in order to prevent the evaporation, or, on the other hand, the absorption of appreciable quantities of moisture during the operation. The above sample bottles are handed over to the laboratory chemist, who has to pulverise their contents till they pass com- pletely through a sieve with holes 1 mm. (=^ in.) wide; no coarse material must be left behind. From this, after thorough mixing, a smaller sample is taken and reduced to the degree of division necessary for analysis, by grinding in a steel or agate mortar, in the case of softer substances in a porcelain mortar. Manganese samples should not be treated in iron mortars. Moisture is estimated in an unground portion of the sample. (b) Orei in pieces requiring to be crushed. — Large-sized samples must be taken if the lumijs of the ore are very coarse. If the pieces are not above the size of an apple, and not too unequal, it is sufficient to take a sample from each tub, etc., as in (a), but with a shovel or scoop holding about 10 lbs. In the case of larger lumps, and of very unequal sizes, it is preferable to tip every tenth or twentieth tub or cart into a separate place, where the whole average sample is collected. In any case, the pro- portion between the large and small pieces must be represented as accurately as possible in the average sample. This is then crushed to the size of a walnut, either by hand or by machinery, leaving no larger lumps behind. The crushed material is thoroughly mixed by turning it over with a spade several times ; * At some factories very nnaatisractory results have been obtained with this mode of sampling ; they prefer that described later on (in &), viz., taking a certain number of entire tubs, barrows, or carts as sample. RULES FOR SAMPLING 251 it ig tten spread out in a flat heap and a smaller sample of about i cwt. is taken, by lifting out two strips, crossing' each other at right angles, adding something from the centre of each remaining quadrant. The reduced sample is crushed further, either in a large metal mortar, or preferably with a sledge hammer on _ a flanged cast-iron plate about 3 ft. square, bedded on a solid foundation ; the latter process is much more convenient and cleanly than grinding in a mortar. The coarse portions are sifted out by a riddle of ^-in. holes and crushed again, till all has passed through. The product is reduced as in (a), by mixing, etc., to a quantity of 2 or 4 lbs., from which the sample bottles are filled as described above. O. — Chemicals. Saltcahe, soda ash, etc., if in bulk, are sampled as in No. 1, (a). If packed in casks, each third, fifth, or tenth cask, according to the size of the parcel, is bored at one of its bottoms and sampled by means of an auger (Fig. 20), which is inserted up to the centre of the cask, turning it round its axis all the while. The single cask samples are put into a large wide-mouthed bottle, as drawn, tiU the sampling is over. Then empty the whole on to a large sheet of paper, mix thoroughly, crush any lumps with a spatula, and fill the 4-ounce bottles, previously prepared, exactly as described in No. 1 as for ores, observing the simple rules for corking and sealing. Bleaching powder, potash, and any other substances which are liable to be quickly spoilt in contact with the air by attract- ing moisture, or from othet reasons, are treated like the foregoing substances, but operating with the greatest possible speed, and keeping the large bottles for collecting the cask samples well closed. The sampling is still more safely performed by taking away the upper end of the cask, removing the top layer to a depth of about 2 inches, taking a handful of the material from the interior as far as it is possible to reach in, which should be nearly at the centre of the cask, and placing it in the large bottles. In this way there is the least contact with air. Or else a sample-auger is employed, like that shown in Fig. 21, p. 252. It is made of a piece of gas-pipe of 1^-inch bore, cut open for part of its length, so that a longitudinal slot of 1 inch width, a, is formed. One side of the slot is sharpened, as well as the tip 6, which is driven into the bleaching powder, etc. The upper part of the pipe is left uncut, and is provided with a handle, c. Before introducing the auger the cask is well shaken up; then it is placed in an upright 252 THE TECHNICAL CHEMISTS' HANDBOOK position and the auger is driven in as deeply as possible, in case of need by the aid of a hammer. This is done either after opening the cask, or by boring a hole in the end, which is afterwards closed by a piece of tin, with paper underneath. After driving in the auger, it is turned several times round its axis, so that it cuts through the bleaching powder with its sharp side and is thus filled up with it. The sample drawn out is put on paper, and is crushed on this as quickly as possible, preferably by means of a small hand-roller ; it is then mixed and spread out flat. Small samples are finally taken from various parts by means of a spatula, as quickly as possible, and are put into bottles, which are tightly closed and kept in a dark place. Bleaching-powder samples should be always tested with as little delay as possible. PlQ. 21. Caustic soda. — Since the samples attract moisture and carbonic acid on their surface, even in well-closed bottles, the outer opaque crust must be removed by scraping before weighing out the samples (c/. p. 198). It should be borne in mind that the centre of the drum is of weaker strength than the remainder, because the foreign salts accumulate in the portion which remains liquid the longest. The average strength is best represented by the portions next to the bottom and sides of the drum, which sohdify quickest. This is most conveniently done while the contents are still in the liquid state. For the control of the manufacture itself it is best to take samples out of every pot during the time its contents are ladled out, from the top, the centre, and the bottom. These are poured out on to a metal plate, where they quickly solidify. The centre sample is the most important one forjudging of the quality of each pot. Solid sulphuric anhydride cannot be sampled directly for analysis. An auger cannot be employed, as the mass is too firm and tough ; melting the mass in the drums themselves is out of the question, on account of the clouds of fumes. The following process is, therefore, employed :— A large sample of the solid anhydride is mixed with so much exactly analysed " mono- hydrated " sulphuric acid that an acid of about 70 per cent, is formed, which is liquid at ordinary temperatures. This mixture is made in a stoppered bottle, and is gently heated to 30° or 40° C., the stopper being loosely put in till the solution is complete, and a small sample then taken out by means of Lunge and Key's glass-tap pipette (p. 145). COMPARISON OF HYDROMETER DEGREES 253 XIX. COMPARISON OF THB HVDBOMETER DSaBEBS ACCORDING TO BAUMiE! AND TWADDELL, WITH THE SPBCIPIC GRAVITIES. B. T. Spec. Gravity. B. T. Spec. Gravity. B. T. Spec. Gravity. 1-000 15-4 24 1-120 29-3 51 1-265 0-7 1 1-005 16-0 25 1-126 29-7 52 1-260 1-0 1-4 1-007 16-5 26 1-130 30-0 62-6 1-263 1-4 2 1-010 17-0 26-8 1-134 30-2 53 1-265 2-0 2 -a 1-014 17-1 27 1-135 30-6 54 1-270 2-1 3 1-015 17-7 28 1-140 31-0 54-8 1-274 2-7 4 1-020 18-0 28-4 1-142 31-1 55 1-276 3-0 4-4 1-022 18-3 29 1-145 31-5 56 1-280 3-4 5 1-025 18-8 30 1-150 32-0 57 1-285 4-0 5-8 1-029 19-0 30-4 1-152 32-4 58 1-290 4-1 6 1-030 19-3 31 1-155 32-8 59 1-295 4-7 7 1-035 19-8 32 1-160 33-0 59-4 1-297 5-0 7-4 1-037 20-0 32-4 1-162 33-3 60 1-300 5-4 8 1-040 20-3 33 1-166 33-7 61 1-305 - 6-0 9 1-046 20-9 34 1-170 34-0 61-6 1-308 6-7 10 1-050 21-0 34-2 1-171 34-2 62 1-310 7-0 10-2 1-062 21-4 35 1-175 34-6 63 1-316 7-4 11 1-055 22-0 36 1-180 36-0 64 1-320 8-0 12 1-060 22-5 37 1-185 35-4 65 1-325 8-7 13 1-065 23-0 38 1-190 35-8 66 1-330 9-0 13-4 1-067 23-5 39 1-196 36-0 66-4 1-332 9-4 14 1-070 24-0 40 1-200 36-2 67 1-335 10-0 16 1-075 24-5 41 1-205 36-6 68 1-340 10-6 16 1-080 25-0 42 1-210 37-0 69 1-345 11-0 16-6 1-083 25-5 43 1-216 37-4 70 1-350 11-2 17 1-085 26-0 44 1-220 37-8 71 1-366 11-9 18 1-090 26-4 45 1-225 38-0 71-4 1-357 12-0 18-2 1-091 26-9 46 1-230 38-2 72 1-360 12-4 19 1-095 27-0 46-2 1-231 38-6 73 1 -365 13-0 20 1-100 27-4 47 1-236 39-0 74 1-370 13-6 21 1-105 27-9 48 1-240 39-4 75 1-375 14-0 21-6 1-108 28-0 48-2 1-241 39-8 76 1-380 14-2 22 1-110 28-4 49 1-245 40-0 76-6 1-383 14-9 23 1-115 28-8 50 1-250 40-1 77 1-385 ]5-0 23-2 1-116 29-0 50-4 1-252 40-5 78 1-390 144-3 , water of 16" C. N.B.—Th.Q Baum6 degrees are calculated by the formula (i= ^ 144'3-n. being put=0'' and sulpburic acid of 1'842 at 15° 0.=66°. This is the Baum^'a hydro- meter, mostly used on the Continent of Europe, but other scales are in use there as well, and quite another scale for Baume's hydrometer is used in America. 254 THE TECHNICAL CHEMISTS' HANDBOOK COMPARISON OF THB HYDBOMBTBR DSGBEiES ACCORD- ING TO BAUM^ AND TWADDBLL, WITH THE SPECIFIC GRAVITIES- B. T. Spec. Gravity. B. T. Spec. Gravity. B. T. Spec. Gravity. 40-8 79 1-395 50-9 109 1-545 59-5 140 1-700 41-0 79-4 1-397 51-0 109-2 1-546 59-7 141 1-705 41-2 80 1-400 51-2 110 1-550 60-0 142 1-710 41-6 81 1-405 51-5 111 1-565 60-2 143 1-715 42-0 82 ^ 1-410 51-8 112 1-560 60-4 144 1-720 42-3 83 1-415 52-0 112-6 1-563 60-6 145 1-725 42-7 84 1-420 52-1 113 1-565 60-9 146 1-730 . 43-0 84-8 1-424 52-4 114 1-570 61-0 146-4 1-732 43-1 85 1-425 52-7 115 1-575 61-1 147 1-735 43-4 86 1-430 53-0 116 1-580 61-4 148 1-740 43-8 87 1-435 53-3 117 1-585 61-6 149 1-745 44-0 87-6 1-438 53-6 118 1-590 61-8 150 1-750 44-1 88 1-440 53-9 119 1-695 62-0 150-6 1-763 44-4 89 1-445 54-0 119-4 1-597 62-1 151 1-765 44-8 90 1-450 54-1 120 1-600 62-3 152 1-760 45-0 90-6 1-453 54-4 121 1-605 62-5 153 1-765 45-1 91 1-455 54-7 122 1-610 62-8 154 1-770 45-4 92 1-460 55-0 123 1-615 63-0 156 1-775 45-8 93 1-465 65-2 124 1-620 63-2 156 1-780 46-0 93-6 1-468 55-5 125 1-625 63-6 167 1-785 46-1 94 1-470 55-8 126 1-630 63-7 158 1-790 46-4 95 1-475 56-0 127 1-635 64-0 159 1-795 46-8 96 1-480 56-3 128 1-640 64-2 160 1-800 47-0 96-6 1-483 56-6 129 1-645 64-4 161 1-805 47-1 97 1-485 56-9 130 1-650 64-6 162 1-810 47-4 98 1-490 57-0 130-4 1-652 64-8 168 1-815 47-8 99 1-495 57-1 131 1-655 65-0 164 1-820 48-0 99-6 1-498 57-4 132 1-660 65-2 166 1-825 48-1 100 1-500 57-7 133 1-666 65-5 166 1-830 48-4 101 1-605 57-9 134 1-670 65-7 167 1-836 48-7 102 1-510 68-0 134-2 1-671 65-9 168 1-840 49-0 103 1-515 68-2 135 1-676 66-0 168-4 1-842 49-4 104 1-520 68-4 136 1-680 66-1 169 1-845 49-7 lOS 1-525 68-7 137 1-685 66-3 170 . 1-850 50-0 106 1-630 58-9 138 1-690 66-5 171 1-855 50-3 107 1-535 59-0 138-2 1-691 66-7 172 1-860 50-6 108 1-540 69-2 139 1-695 67-0 173 1-865 VALUE OF ALKALI PER TON 255 XX. VALUE OF ALKALI PER TON. Price per unit. 1 per cent. 2 per cent. 8 per cent. 1 4 per cent. 5 per cent. Pence. £ s. d. £ s. d. £ s. d. £ s. d. £ s. d. i 1 3 2 6 3 9 5 6 3 a 1 4i 2 81 4 Oi 5 5 6 9i i 1 5i 2 11 4 4i 5 10 7 84 \i 1 6i 3 14 4 8i 6 3 7 9J 1 1 8 3 4 5 6 8 8 4 1^ 1 9i 3 6i 5 3J 7 1 8 lOi n 1 104 3 9 5 74 7 6 9 44 lA 1 111 3 llj 5 Hi 7 11 9 lOi li 2 1 i 2 6 3 8 4 10 5 lA 2 2i 4 4i 6 6i 8 9 10 llj 1| 2 3i 4 7 6 104 9 2 11 54 liV 2 4i 4 9i 7 2i 9 7 11 llj 14 2 6 5 7 6 .0 10 12 6 lA 2 7i 5 24 7 9i 10 5 13 Oi If 2 84 5 5 8 li 10 10 13 64 m 2 9i 5 74 8 5i 11 3 14 Oj If 2 11 6 10 8 9 11 8 14 7 lit 3 Oi 6 Oi 9 Of 12 1 15 li IS 3 14 6 3 9 44 12 6 15 7i IH 3 2i 6 54 9 8J 12 11 16 IJ 2 3 4 6 8 10 13 4 16 8 2A 3 5J 6 lOi 10 3i 13 9 17 2J 2i 3 6i 7 1 10 74 14 2 17 84 2A 3 7| 7 3i 10 Hi 14 7 18 2j 2i 3 9 7 6 11 3 15 18 9 2A 3 lOi 7 8J 11 6| 15 5 19 3J 2f 3 Hi 7 11 11 104 15 10 19 9i 2A 4 Of 8 14 12 2i 16 3 1 3f 2i 4 2 8 4 12 6 16 8 1 10 To find the value of intermediate strengths not given in tlie table, lor instance- i oer cent, at 1 A per unit, find for 80 per cent £3 6 7^ ^ then for 6 „ 13 I^ The sum gives the value per ton of 86 „ £3 18 9 256 THE TECHNICAL CHEMISTS' HANDBOOK VALUE OP ALKALI FEB TON— Continued. Price per unit. 6 per cent. 7 per cent. 8 per cent. 9 per cent. 10 per cent. Pence. £ s. d. £ s. d. £ s. d. £ s. d. £ s. d. 1 7 6 8 9 10 11 3 12 6 i% 8 14 9 5i 10 10 12 21 13 64 i 8 9 10 24 11 8 13 14 14 7 a 9 44 10 llj 12 6 14 Of 15 7i 1 10 11 8 13 4 15 16 8 ^-h 10 74 12 4| 14 2 15 Hi 17 84 14 11 3 13 14 15 16 104 18 9 lA 11 104 13 10| 15 10 17 9i 19 94 li 12 6 14 7 16 8 18 9 1 10 lA 13 14 15 3i 17 6 19 H 1 1 104 If 13 9 16 04 18 4 1 n 1 2 11 1/. 14 4J 16 9J 19 2 1 1 6| 1 3 114 H 15 17 6 1 1 2 6 1 5 lA 15 74 ■0 18 2f 1 10 1 3 5i 1 6 04 If 16 3 18 114 1 1 8 1 4 44 1 7 1 li* 16 104 19 8| 1 2 6 1. 5 Si 1 8 14 IS 17 6 1 5 1 3 4 1 6 3 1 9 2 m 18 IJ 1 1 If 14 2 1 7 2i 1 10 24 u 18 9 1 1 104 15 1 8 14 1 11 3 Hi 19 44 1 2 7i 1 5 10 1 9 Of 1 12 34 2 10 1 3 4 1 6 8 1 10 1 13 4 2-^ 1 74 1 4 Of 1 7 6 1 10 Hi 1 14 44 24 1 1 3 1 4 94 18 4 1 11 104 1 15 5 2A 1 1 104 1 5 6i 1 9 2 1 12 9f 1 16 54 2i 12 6 1 6 3 1 10 1 13 9 1 17 6 2A 1 3 14 1 6 Hi 1 10 10 1 14 8i 1 18 64 2i 1 3 9 1 7 84 1 11 8 1 15 74 1 19 7 2A 1 4 44 1 8 5i 1 12 6 1 16 6i 2 74 24 15 19 2 1 13 4 1 17 6 2 1 8 To find the value of intermediate strengths not given in the table, for instance- BB per cent, at lA per unit, find for 80 per cent £3 6 7i then for 6 „ 13 l| The sum gives the value per ton of 36 , £3 18 9 VALUE OF ALKALI PER TON 257 VALUE OP ALKALI PER TON— Continued. Price per unit. 20 per cent. 80 per cent. 40 per cent. 48 per cent. 60 per cent. Pence. £ s. d. £ 6. d. £ s. d. £ s. d. £ s. d. . 1 1 5 1 17 6 2 10 3 3 2 6 M 1 7, 1 2 7* 2 14 2 3 5 3 7 84 i 19 2 2 3 9" 2 18 4 3 10 3 12 11 a 1 11 3 2 6 lOi 3 2 6 3 15 3 18 14 1 1 13 i 2 10 3 6 8 4 4 3 4 lA 1 15 5 2 13 li 3 10 10 4 5 4 8 64 14 1 17 6 2 16 3 3 16 4 10 4 13 9 lA 1 19 .7 2 19 ii 3 19 2 4 16 4 18 11-; li 2 1 8 3 2 6 4 3 4 5 5 4 2 lA 2 3 9 3 5 74 4 7 6 5 5 5 9 44 ^ 2 5 10 3 8 9 4 11 8 5 10 5 14 7 lA 2 7 11 3 11 lOi 4 15 10 5 15 5 19 94 14 2 10 3 15 5 6 6 6 lA 2 12 1 3 18 14 5 4 2 6 5 6 10 2J li 2 14 2 4 1 3 5 8 4 6 10 6 16 5 iH 2 16 3 4 4 44 5 12 6 6 15 7 74 11 2 18 4 4 7 6 5 16 8 7 7 6 10 IB 3 5 4 10 74 6 10 7 5 7 11 04 ij 3 2 6 4 13 9 6 5 7 10 7 16 3 iH 3 4 7 4 16 104 6 9 2 7 15 8 1 54 2 3 6 8 5 6 13 4 8 8 6 8 2A 3 8 9 5 3 14 6 17 6 8 5 8 11 lOA 2i 3 10 10 5 6 3 7 1 8 8 10 8 17 1 2A 3 12 11 5 9 44 7 5 10 8 15 9 2 34 2i 3 15 5 12 6 7 10 9 9 7 6 2A 3 17 1 5 15 74 7 14 2 9 6 9 12 84 2f 3 19 2 5 18 9 7 18 4 9 10 9 17 U 2-^^ 4 1 3 6 1 104 8 2 6 9 15 10 3 14 2i 4 3 4 6 6 8 6 8 10 10 8 4 To find the value of intermediate strengths not given in the table, for instance- i per cent, at 1,^ per unit, find for 30 per cent £3 5 7i then for 6 „ IS li The sum gives the value per ton ot'Sti ,, £3 18 258 THE TECHNICAL CHEMISTS' HANDBOOK VALUE OP AIiKAIiI PER "VO^— Continued. Price per unit. 52 per cent. 54 per cent. 66 per cent. 57 per -ent. 58 per cent. Pence. £ s. d. £ s. d. £ s. d. £ s. d. £ s. d. i 3 5 3 7 6 3 10 3 11 3 3 12 6 \i 3 10 5 3 13 14 3 16 10 3 17 24 3 18 64 s 3 15 10 3 18 9 4 1 8 4 3 14 4 4 7 H 4 1 3 4 4 44 4 7 6 4 9 0| 4 10 74 1 4 6 8 4 10 4 13 4 4 15 4 16 8 itV 4 12 1 4 15 74 4 19 2 5 Hi 5 2 84 1* 4 17 6 5 1 3 5 5 5 6 104 5 8 9 lA 5 2. 11 5 6 104 5 10 10 5 12 9S 5 14 94 li 5 8 4 5 12 6 5 16 8 5 18 9 6 10 lA 5 13 9 5 18 14 6 2 6 6 4 8i 6 6 104 IS 5 19 2 6 3 9 6 8 4 6 10 74 6 12 11 lA 6 4 7 6 9 44 6 14 2 6 16 6i fi 18 114 li 6 10 6 15 7 7 2 6 7 5 lA 6 15 6 7 74 7 5 10 7 8 H 7 11 04 i§ 7 10 7 6 3 7 11 8 7 14 44 7 17 1 m 7 6 3 7 11 104 7 17 6 8 3! 8 3 14 If 7 11 8 7 17 6 8 3 4 8 6 3 8 9 2 Its 7 17 1 8 3 14 8 9 2 8 12 2i 8 15 24 n 8 2 6 8 8 9 8 15 8 18 14 9 1 3 w 8 7 11 8 14 44 9 10 9 4 OS 9 7 34 2 8 13 4 9 9 6 8 9 10 9 13 4 2A 8 18 9 9 5 74 9 12 6 9 15 "i 9 19 44 24 9 4 2 9 11 3 9 18 4 10 1 104 10 5 5 2A 9 9 7 9 16 104 10 4 2 10 7 91 10 11 54 2i 9 15 10 2 6 10 10 10 13 9 10 17 6 2A 10 5 10 8 14 10 15 10 10 19 8i 11 3 64 2S 10 5 10 10 1» 9 11 1 8 11 5 74 11 9 7 2A 10 11 3 10 19 44 11 7 6 11 11 6f 11 15 74 2* 10 16 8 11 5 11 13 4 11 17 6 12 1 8 To find the value of intermediate strengths not given in the table, for instance- 86 per cent, at 1 ,», per unit, find for 30 per cent £8 5 7i thenfor 6 18 ij The sum gives the value per ton of 86 , £3 18 9 INDEX Acetylene, 228 Acid, free, in fertilisers, 232 in sulphate of alumina, 237 standard, preparation of, 243 Acids in chambers, 117 Air compression, 59 ^ currents, speed of, 99 tables of, 100 Alkali available in black-ash, 167 in tank waste, 168 in soda ash, 178 total, in tank waste, 169 free, in bleach liquors, 194 standard, preparation of, 245 value per ton, 255 Alkalimetrical degrees, 179 table of, 180 Alumina, commercial, 237 preparations, 234 sulphate of, 235 in fertilisers, 232 Aluminate of soda, 237 Ammonia manufacture, 217 volatile, 217 total, 217, 219 solutions, specific gravities of, 221 carbonate, specific gravities of solu- tions, 222 sulphate, 219 Ammoniacal brine, 185 Ammonia-soda process, 185 Anemometer, Fletcher's, 99 tables for, 100 Seger's, 102 Aqueous vapour, tension at various tem- peratures, 52, 53 Area of circles, etc., table of, 63 Arsenic, estimation in brimstone, 106 in pyrites. 111 259 Ai'senic, estimation in sulphuric acid, 144 in hydrochloric acid, 154 Arseniteof soda, standard solution, 248 Ash of fuel, 93 ■ of mixing coal, 164 Atomic weights, 3 Auger for sampling, 251 Available soda. See Alkali Base of Weldon mud, 157 Baum^'s hydrometer, 253 Bauxite, 234 Beet ashes, 207 Belgian method for estimating zinc in blende, 112 Black-ash, 166 Bleach liquors, 164 Bleaching powder, 159 table of percentages, 160 sampling, 251 Bleaching powder chambers, tests before opening them, 161 Blende, 112 cinders from, 114 Boiling points of various substances, 33 of water at various pressures, 57 Bottoms, caustic, 192 Brimstone, analysis, 106 Bunte burette, 223 Burner gases, 115 Burnt pyrites. 111 Calcium carbide, 228 Calorific power of fuel, 95 of coal'gas, 227 Carbon, fixed, in fuel, 93 Carbon dioxide. See Carbonates in Deacon gases 162 260 INDEX Carbon dioxide in electrolytic cliloriue, 163 in carbonated soda liquor, 171 by Lunge and Rittener's method, 171 in coal-gas, 224 monoxide, 224 Carbonated soda liquor, 171 Carbonates in pyrites. 111 in qnicklime, 150 in manganese ore, 155 in bleaching powder or bleach liquors, 160 in caustic soda, 193 Carnallite, 205 Caustic bottoms, 192 liquor, 186 specific gravities, 187 soda, manufacture, 189 in black-ash, 167 commercial, 193 sampling, 252 Cement, Portland, 238, 240 Cements, other, 241 Centigrade degrees, comparison with Fab: renheit, 27, 28, 25 Chamber gases, 116 Chance process, 180 Chancel's sulphuri meter, 108 Chemicals, sampling of, 251 Chimney gases, 95 from chemical works (Act of Parlia- ment), 149 China clay, 234 Chlorate of potash, 164 Chlorates, estimation, 164 by Fresenius's method, 194 by Ditz and En5pfelmacher, 194 Chloride, estimation in common salt, 146 in saltcake, 148 of potassium, 164 ' Chlorine, estimation in salt, 148 Chlorine, free, in hydrochloric acid, 154 in the atmosphere of chambers before opening them, 161 available in bleaching powder, 159 comparison with French degrees, 160 in Deacon gases, 162 electrolytic, 168 liquid, pressure and specific gravities, 165 Cinders from pyrites. 111 from blende, 114 Circumferences, table of, 68 CUus kilns, gases of, 184 Clay, in cement, 238 complete analysis, 23S Coal, 93 mixing, for Leblanc process, 164 gas, 222 Coinage of diflerent countries, 88 Coke, 93 CompoandB, symbols, molecular weights, percentage composition, 4 Compression of air, 59 Copper, estimation in pyrites, 109 in burnt pyrites, 112 solutions, standard, 249 Cubic centimetres in gas -volumetric analyses, calculation to milligrams of the substance required, 15 Cyanogen in spent oxide, 227 Deacon process, 162 Decomposing fiask, 219 Degrees, alkalimetrical, table, 179 Density of gases and vapours, 14 Draught, testing speed of, 9^ Electrical units, 62 Electro-chemical equivalents, 62 Electrolytic chlorine, 163 alkali liquors, 198 English weights and measures, reduction to metrical, 83 Eschka's method for estimating sulphur, 94 Expansion, linear, of substances, 26 Explosive mixtures of gases and air, 60 Factors fob gravtsibtric analyses, 12 Factors for reducing volumes of gases to normal temperature and pressure, 48 Fahrenheit degrees, comparison with Centigrade, 27, 28, 29 Feed-water for steam-boilers, 104 Ferchland's estimation of carbon dioxide, 163 Ferric oxide in fertilisers, 282 Ferrocyanide in tank liquor, 170 Fertilisers, 229 sampling, 229 moisture, 229 estimation of phosphoric acid, 230 free acids, 282 ferric oxide and alumina, 282 nitrogen, 23S Fire gases, 95 Fished salts in caustic soda manufacture, 192 INDEX 261 Fletcher's anemometer, 99 Freezing mixtures, 32 points, SO Fuel, 93 Galorific power of, 95 sampling, 249 Furnaces, 95 Gas-burettes, 222 Gases, density of, 14 solubility in water, 18 reduction of volume to 0° C, 36 to a pressure of 760 mm., 42 toCC. or32°F., 48 factors for the same, 48 Gases, liquefied, properties, 61 See Fire gases, Burner gases, Chimney gas, Chamber gases, etc. ill sulphur recovery (Claus kilns), 184 Gas-liquor, 217 Gas-producers (generators), 97 Gas -volumeter. Lunge's, 139 with decomposing flask, 219 Gas-volumetric analysis, calculation, 15 Gay-LuBsac'sdegreesof bleaching powder, 160 Glass-tap pipette, 145 Gravimetric analysis, factors for, 12 Gravity, specifiCj of gases, 14 of solids, 22 of liquids, 25 of saturated solutions, 25 Hardness of Water, temporary, 104 total, 105 reagents for removing, 105 Hargreaves' process, 151 Heats, specific, 57 Heating effects, 58 High temperatures, 35 Hydraulic lime, 241 Hydrocarbons in coal-gas, 224 Hydrochloric acid in chimney gases, 149 specific gravities, 152 influence of temperature on, 153 analysis, 153 estimation of HCl, 153 of impurities, 154 estimation of acid required for decom- posing manganese ore, 156 standard, 243 Hydrogen in coal-gas, 225 sulphide, 184 Hydrometer degrees, comparison of, 253 Hypochlorites, 159 Hypochlorous acid, free, 193 Indicators, 243 International atomic weights, 3 Iodine in nitrate of soda, 196 in nitric acid, 203 solution, standard, 247 Iron in burnt pyrites, 112 in sulphuric acid, 143 in sulphate of soda, 143 in hydrochloric acid, 154 in sulphate of alumina, 236 Kainitb, 205 Kaolin, 234 Kjeldahl-Jodlbauer's mathod for estimat- ing nitrogen, 233 Lead, in pyrites, 110 in blende, 114 in sulphuric acid, 143 chambers. Bee Chambers Leblanc process, 166 raw materials, 166 black-ash, 166 tank waste, 169 liquor, 170 carbonated liquor, 171 mother liquor, 173 sulphur recovery, 182 Le Chatelier's pyrometer, 103 Lime, estimation in blende, 114 in salt, 147 in saltcake, 14S in limestone, 157 caustic, 158 quick, 158 slaked, 158 milk of, 15S specific gravities of milk of, 159 in black-ash, 166 hydraulic, 241 Lime-kiln gases, 183 Lime mud in caustic soda manufacture, 192 Limestone, 157, 238 Linear expansion of substances, 26 Liquefied gases, properties, 61 Liquor ammonisB, 220 Litmus, 244 Litre weights of gases, 14 Lunge's formula for testing the work of furnaces, 97 262 INDEX Lunge-Orsat apparatus, 198 Lunge's nitrometer, 137 gas-volumeter, 139, 219 reagent for nitrous acid , 143 glasB-tap pipette, 145 Lunge and Bittener's method for estimat- ing carbon dioxide, 171 and K^ler's method for estimating small quantities of iron, 236 and Millberg's^ separation of quartz from silicates, 239 Magnesium salts in potassium chlor- ide, 206 Manganese ore, natural, 155 sampling, 249 dioxide, estimation, 165, 156 mud, recovered, 156 Manures. See Fertilisers Mathematical tableSf 63 Measures and weights of different coun- tries, 79 Melting points, 30 Mensuration of areas and solid contents,77 Metals, sheets, weight of, 87 Methane in coal-gas, 226 Methyl orange, 244 Metrical weights and measures, reduction to English, 83 Minerals, sampling of, 249 Mixing>coal, 166 Molecular weights of compounds, 4 Molybdenum method for phosphates, 231 Mother liquor of Leblanc soda, 173 Muriatic acid. See Hydrochloric acid Nitrate of Soda, 195 NitrO'Cake, 197 Nitric acid, manufacture of, 195 specific gravities, 198 influence of temperature, 201 titration, 203 impurities, 203 mixtures with sulphuric acid, 204 oxide, 119 Nitrogen, in coal-gas, 226 acids, estimation in chamber gases, 116 in sulphuric acid, 135 relative proportions of, 142 qualitative test for, 142 in fertilisers, 238 nitric-, 283 total, 283 Nitrogen, organic, 238 Nitrometer, Lunge's, 137, 195 Nitrous acid, estimation for, in sulphuric acid, 136 Nitrous acid, detection of very small quantities, 148 in commercial nitric acid, 208, 204 Nordhausen oil of vitriol, specific gravi- ties, 130 at different temperatures, 131 fusing points, 188 percentage of SO3 in, 184 analysis, 144 Normal acid and alkali, etc. See Stand- ard Oil of vitriol. See Nordhausen oil of vitriol Ores, sampling of, 249 Orsat apparatus, 95 Orsat-Lunge apparatus, 98 Oxalic acid, standard aolation, 249 Oxygen in chamber gases, 117 in coal-gas, 224 Palladium tube, 225 Percentage composition of compounds, 4 Perchlorates, 197 Permanganate solution, standard, 246 Phosphates, 230 Phosphoric acid, soluble, 230, 281 total, 230, 231 Portland cement, 238 raw materials, 238 working conditions, 240 commercial, 240 Potash in fertilisers, 234 chlorate of, 164 Potassium, estimation, 205 carbonate, commercial, 207 specific gravities of solutions, 209 influence of temperature, 212 chloride, 205, 207 salts, 205 sulphate, 207 hydroxide, specific gravities, 214 ' nitrate in commercial nitrate of soda, 197 perchlorate, 197 permanganate, standard solution, 246 Pressure of gases, reduction to normal, 40 of water, reduction to mercurial pres- sure, 51 I^TDEX 263 Producer gas, 97 Purifying material of gas-works, 227 water, reagents for, 107 Fuzzuolanas, 241 Pyrites, 108 burnt, 111 burner gases, 115 sampling, 249 Pyrometer, Le Chatelier's, 103 Wanner's, 104 indications of, 35 Quartz in cement, 239 Reich's test for burner gases, 115 Kock-salt, 146 Roman cement, 289 Salt, common and rock-, 146 sampling, 249 Saltcake, 147 Salts, fished, in caustic-soda manufac- ture, 192 Salts, solubility of, 10, 17 Sampling, rules for, 249 auger, 251 Seger's anemometer, 102 Selenium, in brimstone, 106 in sulphuric acidj 143 Sheet metals, weight, 87 Silica in cement, 239 Silver solution, standard, 24S Slags, 241 Soda, available. See Alkali ash, commercial, 178 manufacture by Leblanc process, 166 raw materials for, 166 by ammonia process, 185 caustic, manufacture, 186. See Sodium hydroxide and Standard alkali Sodium arsenite, standard solution, 248 estimation in caustic soda, 193 carbonate solutions, specific gravities of, at 15*, 174 ; at 30% 175 influence of temperature, 176 pure, for standardising, 243 hydroxide, 168 specific gravities, 187 iniluence of temperature, 190 Sodium nitrate, 195 salts in commercial potassium chloride, 206 silicate, 179 Solubility of gases in water, 18 of salts at 0° and 100% 16 at various temperatures, 17 Solutions of salts, specific gravity, 25 Specific gravities, of solids, 22 of gases, 14 of liquids, 25 of saturated solutions, 25 comparison of hydrometers, 253 heats, 57 Spent oxide of gas-works, 108, 227 Standard solutions, general, 241 comparison of English and French systems, 241 influence of temperature on, 246 acid, 242 alkali, 245 permanganate, 246 iodine, 247 sodium arsenite, 248 silver, 248 copper, 249 oxalic acid, 249 Starch solution, 247 Steam-boilers, feed-water, 104 Storage weights of substances, 24 Sulphate of soda, 147 Sulphide of sodium, 168, 178 Sulphur, in fuel, 94 in mixing coal, 166 in brimstone, 107 in pyrites, 108 in burnt pyrites, 111 in blende, 112 in cinders from blende, 114 in tank waste, 169, 182 in gas-liquor, 217 in spent oxide, 227 specific gravities of solutions of, in carbon disulphide, 107 acids of, in chamber gases, 116 compounds, in soda liquors, 173 dioxide in chamber gases, 115 in hydrochloric acid, 154 recovery from tank waste, 182 Sulphur compounds, various, in Leblanc liquors, 173 Sulphuric acid, ordinary, quantitative examination of free acid, 135 examination for nitrous acid, 185 for total nitrogen acids, 137 relative proportions of, 142 qualitative test for nitrogen acids, 142 264 INDEX Sulphuric acid^ other impurities, 148 manufacture, raw materials, 106 gases, 115 Sulphuric acid, specific gravities at 60' F., 121 reduction to other temperatures, 126 freezing and melting points, 132 boiling points, 132 fusing points of, and of Nordhausen oil of vitriol, 138 mixtures with nitric acid, 204 fuming. See Nordhausen oil of vitriol anhydride, analysiB, 144 sampling, 252 Sulphurimeter, Chancel's, lOS Symbols of compounds, 4 Tank liquor, 169 waste, 168, 182 Temperature, reduction of gases to nor- mal, 36 Temperatures, high, measured by pyrom- eter, 35 measurement of, 102 Tension ot aqueous vapour at various temperatures, 52, 53, 55 Thermometers, conversion of Centigrade into Fahrenheit degrees above 100% and vice versa, 29 Thermometric scales, comparison, Centi- grade degrees as units, 27 Fahrenheit degrees as units, 28 above 100°, 29 Thiocyanate, 218 Thomas-slag phosphates, 231 Titanic acid, 235 Trass, 241 TwaddeU's hydrometer, 253 Vapours, density of, 14 Vat liquor, 170 waste, 169 Vitriol chambers. See Chambers, Volume of gases, reduction to normal temperatures and pressure, 36 Volumes of water at dififerent tempera- tures, 51 Wanner's pyrometer, 104 Water, hardness, temporary, 104 total, 105 pressure, reduction to mercurial pres- sure, 51 volumes at different temperatures, 51 vapours, tension of, 52, 53, 55 boiling points at various pressures, 57 reagents for purifying, 105 Weight of sheet metals, 87 of substances as stored, 24 Weights and measures of different coun- tries, 87 reducing English to metrical, and vice versa, 83 Weldon mud and liquors, 156 Zinc in pyrites, 110 in blende, 112 in sulphate of alumina, 237 blende, 112 cinders from, 114 solution, 227 PIlINTiilD BY OLIVER AND BOVD, EDINBURGH, SCOTLAND.