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A Text-book of Assaying: For the Use of Those Connected with Mines.
اقرأ عينة مجانية

A Text-book of Assaying: For the Use of Those Connected with Mines.

بقلم Beringer J J (John Jacob)

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A TEXT-BOOK OF ASSAYING:

FOR THE USE OF THOSE CONNECTED WITH MINES.

BY

C. AND J. J. BERINGER.

REVISED BY

J. J. BERINGER,

ASSOC. OF THE ROYAL SCHOOL OF MINES; FELLOW OF THE CHEMICAL SOCIETY AND OF THE INST. OF CHEMISTRY; PRINCIPAL OF THE CAMBORNE MINING SCHOOL; AND LATE PUBLIC ANALYST FOR THE COUNTY OF CORNWALL.

With numerous Diagrams and Tables.

NINTH EDITION.

 

 

LONDON:
CHARLES GRIFFIN AND COMPANY, Limited,
EXETER STREET, STRAND.

1904.

[All rights reserved.]


PUBLISHER'S NOTE TO THE NINTH EDITION

The continued popularity of the present work, the last edition of which was published only a little over a year ago, continues to be a source of gratification to the publishers, who have much pleasure in issuing the present edition.

    January 1904.


PREFACE TO THE SIXTH EDITION

The principal changes in this edition are additions to the articles on Gold, Cyanides, and Nickel, and a much enlarged Index. The additional matter covers more than forty pages.

J. J. BERINGER.

Camborne,
January 1900.


PREFACE.

The Text-book now offered to the public has been prepared to meet the existing want of a practical "handy book" for the Assayer.

To mining men the word "assaying" conveys a sufficiently clear meaning, but it is difficult to define. Some writers limit it to the determination of silver and gold, and others imagine that it has only to do with "furnace-work." These limitations are not recognised in practice. In fact, assaying is becoming wider in its scope, and the distinction between "assayers" and "analysts" will in time be difficult to detect. We have endeavoured rather to give what will be of use to the assayer than to cover the ground within the limits of a faulty definition.

At first our intention was to supply a description of those substances only which have a commercial value, but on consideration we have added short accounts of the rarer elements, since they are frequently met with, and occasionally affect the accuracy of an assay.

Under the more important methods we have given the results of a series of experiments showing the effect of varying conditions on the accuracy of the process. Such experiments are often made by assayers, but seldom recorded. Statements like those generally made—that "this or that substance interferes"—are insufficient. It is necessary to know under what conditions and to what extent.

Students learning any particular process cannot do better than repeat such a series of experiments. By this means they will, at the same time, acquire the skill necessary for performing an assay and a confidence in their results based upon work under different conditions.

The electrolytic method of copper assaying given under Copper is a modification of Luckow's; it was introduced by us into the offices of the Rio Tinto Copper Company, and has been in use for many years with success. This modification is now employed in copper-works in Spain, Germany, and England, and is used in place of the dry assay for the commercial valuation of copper ores.

We have adhered to the gram and the "c.c." as the units of weight and volume. Those who prefer working with grains and grain-measures can use the figures given, multiplied by ten. For example:—When 1 gram is mentioned, 10 grains should be used, and 10 grain-measures take the place of 1 "c.c." It is not advisable to mix the two systems, as by using gram weights and grain-measures.

We have intentionally to a large extent omitted to mention the names of those who have originated or modified the various processes. The practice of naming a process after its discoverer has developed of late years, and is becoming objectionable. It is a graceful thing to name a gas-burner after Bunsen, or a condenser after Liebig; but when the practice has developed so far that one is directed to "Finkenerise" a residue, or to use the "Reichert-Meissl-Wollny" process, it is time to stop.

We are indebted to the standard works of Allen, Crookes, Fresenius, Lunge, Michell, Percy, and Sutton, and wish to express our sense of special indebtedness to Mr. Richard Smith, of the Royal School of Mines. One or two of the illustrations are taken from Mr. Sexton's excellent little book on Qualitative Analysis. Our obligation to some others is mentioned in the text.

Finally, we have to thank for assistance in the experimental work Messrs. Bailey, Beswick, Clarke, Grant, Higgins, and Smith.

THE AUTHORS.

Camborne,   Nov. 1889.


CONTENTS.

PART I.   CHAPTER I. INTRODUCTORY. Page Object of assaying 1 Sampling 1 Drying: determination of moisture 5 Calculation and statement of results 7 Laboratory books and report forms 9 Quantity to be taken for an assay 11 Exercises 14   CHAPTER II. METHODS OF ASSAYING.—DRY GRAVIMETRIC METHODS. Methods of assaying 15 Gravimetric methods 15
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align="left">Mechanical separations 16 Dry assays 16     (a) Fluxes 16     (b) Reducing agents 21     (c) Oxidising agents 22     (d) Apparatus 24   CHAPTER III. WET GRAVIMETRIC METHODS. Wet gravimetric methods 27     (a) Solution 29     (b) Precipitation 30     (c) Filtration 31     (d) Drying and igniting 32   CHAPTER IV. VOLUMETRIC ASSAYS. Titrometric assays 35     (a) Standard solutions 36     (b) Standardising 37     (c) Methods of working 42     (d) Indirect titration 43 Colorimetric assays 44 Gasometric assays 44   CHAPTER V. WEIGHING AND MEASURING. Weighing 47 Measuring liquids 49     (a) Graduated flasks 49     (b) Pipettes 50     (c) Burettes 51 Measuring gases 52   CHAPTER VI. REAGENTS. Acids, &c. 54 Bases, salts, &c. 59   CHAPTER VII. Formulæ, equations, &c. 68   CHAPTER VIII. SPECIFIC GRAVITY. Introductory 75 Determination of specific gravity—     (a) Hydrometers 76     (b) Specific gravity bottles 78 Calculations depending on specific gravity 84  
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align="left">  PART II.   CHAPTER IX. SILVER, GOLD, PLATINUM, CYANIDES, MERCURY. Silver—Detection 87     Dry assay 87         (1) Scorification 88         (2) Pot assays, average ores 90                 "             ores with metallic oxides 91                 "             ores with metallic sulphides 91     Explanatory notes on the fusion 93     The effect of charcoal, flour, &c. 94     The effect of nitre 95     The effect of mineral sulphides 95         (3) Cupellation 98             The loss of silver 101             Condition affecting the loss 102             Methods of correction 103             Lead required for cupellation 105         (4) Calculation of the results in ounces to the ton of 2240 lbs. Table 107             Ores with metallic particles 108         (5) Explanatory notes 110         (6) Examples of dry silver assays 113     Wet assays 116         Gravimetric method 117         Gay-Lussac's method 119         Volhard's method 121         A modified Gay-Lussac 123         Volhard's method applied to arsenic 124 Gold—Detection 126     Amalgamation assay 126     Dry assay 127         (1) Size of charges 127         (2) Sampling 127         (3) Assay tons 131         (4) Small buttons, weighing
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tag="{http://www.w3.org/1999/xhtml}a">131             "     "       measuring 133         (5) Concentration in lead 136             Quartz ores 136             Ores with oxide of iron 138             Ores with metallic sulphides 139         (6) Cyanide charges, residues, &c. 140         (7) Cupellation 142             Cupels 142             Cupellation temperature 143             Cupellation loss 145         (8) Inquartation 146         (9) Flatting 149         (10) Parting, in flasks 151                 "         in test tubes 152                 "         in glazed crucibles 153                 "         Loss, &c. 154         (11) Check assays, surcharge 154         (12) Bullion assays in special apparatus 156             Silver, &c., in gold bullion 157         (13) Sampling of base bullion, &c. 157 Cyanides—Commercial cyanides 160     Double cyanides 161     Prussic acid 162     Gold-dissolving power of cyanide liquor 162     Assay for cyanide strength 163, 165     Assay of commercial cyanide 167     Alkalinity of cyanides 167     Acidity of ores 168     Metals in cyanide liquors 169     Cyanicides 169 Platinum 170 Iridium 171 Mercury
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href="@public@vhost@g@gutenberg@html@files@18751@[email protected]#Page_171" class="pginternal" tag="{http://www.w3.org/1999/xhtml}a">171     Dry assay 172     Wet method 173   CHAPTER X. COPPER, LEAD, THALLIUM, BISMUTH, ANTIMONY. Copper—Introductory 175     Dry assay 176     Valuation of copper ores 181     Wet methods 183         (1) Electrolytic assay 184     Volumetric methods 194         (1) Cyanide method 194         (2) Iodide method 199         (3) Colorimetric method 203     Examination of commercial copper 205 Lead 211     Dry assay 211     Wet assay 213         (1) Gravimetric method 213         (2) Volumetric method 214         (3) Colorimetric method 218 Thallium 219 Bismuth 220     Dry assay 221     Wet method 221         (1) Gravimetric determination 222         (2) Colorimetric assay 223 Antimony 225     Dry assay 225     Wet method 227         (1) Gravimetric assay 228         (2) Volumetric method 229   CHAPTER XI. IRON, NICKEL, COBALT, ZINC, CADMIUM. Iron 231     Gravimetric determination 233     Permanganate and bichromate methods 234     Stannous chloride method
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href="@public@vhost@g@gutenberg@html@files@18751@[email protected]#Page_244" class="pginternal" tag="{http://www.w3.org/1999/xhtml}a">244     Colorimetric determination 247 Nickel 251     Dry assay 251     Electrolytic assay 254     Titration by cyanide 255 Cobalt 259 Zinc 261     Gravimetric method 262     Volumetric method 263     Gasometric method 266 Cadmium 269   CHAPTER XII. TIN, TUNGSTEN, TITANIUM. Tin 271     Vanning 273     Dry assay 276     Detection, &c. 279     Gravimetric determination 281     Volumetric determination 282     Examples 284 Titanium 292 Tungsten 295 Niobic and Tantalic Oxides 297   CHAPTER XIII. MANGANESE, CHROMIUM, ETC. Manganese 298     Gravimetric determination 300     Volumetric determination 300         Ferrous sulphate assay 301         Iodine assay 302     Colorimetric determination 306 Chromium 307 Vanadium 310 Molybdenum 311 Uranium 312   CHAPTER XIV. EARTHS, ALKALINE EARTHS, ALKALIES. Alumina 314 Thoria
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tag="{http://www.w3.org/1999/xhtml}a">317 Zirconia 317 Cerium 318 Lanthanum and Didymium 319 Yttria 319 Beryllia 319 Lime 320 Strontia 324 Baryta 326 Magnesia 328 The Alkalies 330     Sodium 334     Potassium 336     Lithium 338     Cæsium 339     Rubidium 340     Ammonium 340     PART III.   CHAPTER XV. OXYGEN AND OXIDES—THE HALOGENS. Oxygen 344 Oxides 345 Water 350 The Halogens 358     Chlorine 359     Bromine 361     Iodine 362     Fluorine 363   CHAPTER XVI. SULPHUR AND SULPHATES. Sulphur 367     Gravimetric determination 369     Volumetric determination 370 Sulphates 377 Selenium 379 Tellurium 379   CHAPTER XVII. ARSENIC, PHOSPHORUS, NITROGEN. Arsenic 381     Gravimetric determination 383     Volumetric method, "iodine" 384             "          "         "uranic acetate"
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href="@public@vhost@g@gutenberg@html@files@18751@[email protected]#Page_389" class="pginternal" tag="{http://www.w3.org/1999/xhtml}a">389 Phosphorus 394 Gravimetric determination 396 Volumetric determination 397 Nitrogen and Nitrates 400   CHAPTER XVIII. SILICON, CARBON, BORON. Silicon and Silicates 405 Carbon and Carbonates 414 Coals 418 Shales 420 Carbonates 424 Boron and Borates 429   APPENDIX A. Table of atomic weights and other constants 433 Table for converting degrees of the centigrade thermometer     into degrees of Fahrenheit's scale 435 Tables showing strengths of aqueous solutions of nitric and hydrochloric acids,     of ammonia and of sulphuric acid 436   APPENDIX B. Estimation of small quantities of gold 440 Practical notes on the iodide process of copper assaying 441 Method of separating cobalt and nickel 442   APPENDIX C. A lecture on the theory of sampling 444     Index 450

A TEXT-BOOK OF ASSAYING.


CHAPTER I.

INTRODUCTORY.

Assaying has for its object the determination of the quantities of those constituents of a material which add to or detract from its value in the arts and manufactures. The methods of assaying are mainly those of analytical chemistry, and are limited by various practical considerations to the determination of the constituents of a small parcel, which is frequently only a few grains, and rarely more than a few ounces, in weight. From these determinations calculations are made, which have reference to a mass of material of, perhaps, hundreds of tons. But in all cases, whether the mass under consideration be large or small, whether the material be obtained by mining, grown, or manufactured, the assayer is supposed to receive a small quantity, called "the sample," which is, or ought to be, the exact counterpart of the mass of material that is being dealt with. The taking and making of this sample is termed "sampling"; and the men whose special work it is to select such samples are "the samplers."

But although "sampling" is thus distinct from "assaying," the assayer should be familiar with the principles of sampling, and rigorous in the application of these principles in the selecting, from the sample sent him, that smaller portion upon which he performs his operations.

Sampling.—In the case of gases, there is absolutely no trouble in mixing. The only difficulty is in drawing off a fair sample where, as in flues, the body of the gas is in motion, and varies a little in composition from time to time. In this case, care must be taken to draw off uniformly a sufficient volume of the gas during a prolonged period; any portion of this larger volume may then be taken for the analytical operation.

In the case of liquids, which mix more or less easily—and this class includes metals, &c., in the state of fusion—more or less severe agitation, followed by the immediate withdrawal of a portion, will yield a fairly representative sample.

In the case of solids, the whole mass must be crushed, and, if not already of fairly uniform quality, mixed, before sampling can take place. Most of the material which a sampler is called upon to deal with, is, however, in a more or less divided state and fairly uniform. In practice it is assumed that 5 per cent. of the whole (= 1/20th), if taken in portions of equal weight and at frequent and regular intervals, will represent the mass from which it was taken. Taking a heap of ore, A, and selecting one out of every twenty spade-, bag-, barrow-, or wagon-fuls, according to the quantity of stuff in the heap, there is obtained a second heap, B, containing one-twentieth of the stuff of

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the heap A. If we crush the stuff in B until this heap contains approximately the same number of stones as A did—which means, crushing every stone in B into about twenty pieces—B will become the counterpart of A. Selecting in the same manner 5 per cent. of B, there is got a third heap, C. This alternate reduction and pulverising must be carried on until a sample of suitable size is obtained. This may be expressed very clearly thus:—

A  =  1000 tons of rocks and lumpy ore.
B  =    50      "   "    rough stones,  1/20th of A.
C  =    2.5    "    "    small stones,  1/20th of B.
D  =    0.125  "    "    coarse powder, 1/20th of C.