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Title: A text-book of assaying

for the use of those connected with mines.

Author: C. Beringer

J. J. Beringer


Release date: July 3, 2006 [eBook #18751]

Language: English

Other information and formats: www.gutenberg.org/ebooks/18751

Credits: E-text prepared by Peter Yearsley, Josephine Paolucci, and the Project Gutenberg Online Distributed Proofreading Team

*** START OF THE PROJECT GUTENBERG EBOOK A TEXT-BOOK OF ASSAYING ***

 

E-text prepared by Peter Yearsley, Josephine Paolucci,
and the Project Gutenberg Online Distributed Proofreading Team
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Transcriber's Note:

Parentheses have been added to clarify fractions. Letters in brackets with a = sign before it means that the letters have a macron over them, e.g. H[=A=c] signifies that the Ac has a macron over it.

Minor typographical errors have been corrected. Footnotes have been moved to the end of the chapter, and all advertisements have been moved to the end of the book.

 


 

 

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 assaying1
Sampling1
Drying: determination of moisture5
Calculation and statement of results7
Laboratory books and report forms9
Quantity to be taken for an assay11
Exercises14
 
CHAPTER II.
METHODS OF ASSAYING.—DRY GRAVIMETRIC METHODS.
Methods of assaying15
Gravimetric methods15
Mechanical separations16
Dry assays16
    (a) Fluxes16
    (b) Reducing agents21
    (c) Oxidising agents22
    (d) Apparatus24
 
CHAPTER III.
WET GRAVIMETRIC METHODS.
Wet gravimetric methods27
    (a) Solution29
    (b) Precipitation30
    (c) Filtration31
    (d) Drying and igniting32
 
CHAPTER IV.
VOLUMETRIC ASSAYS.
Titrometric assays35
    (a) Standard solutions36
    (b) Standardising37
    (c) Methods of working42
    (d) Indirect titration43
Colorimetric assays44
Gasometric assays44
 
CHAPTER V.
WEIGHING AND MEASURING.
Weighing47
Measuring liquids49
    (a) Graduated flasks49
    (b) Pipettes50
    (c) Burettes51
Measuring gases52
 
CHAPTER VI.
REAGENTS.
Acids, &c.54
Bases, salts, &c.59
 
CHAPTER VII.
Formulæ, equations, &c.68
 
CHAPTER VIII.
SPECIFIC GRAVITY.
Introductory75
Determination of specific gravity—
    (a) Hydrometers76
    (b) Specific gravity bottles78
Calculations depending on specific gravity84
 
 
PART II.
 
CHAPTER IX.
SILVER, GOLD, PLATINUM, CYANIDES, MERCURY.
Silver—Detection87
    Dry assay87
        (1) Scorification88
        (2) Pot assays, average ores90
                "             ores with metallic oxides91
                "             ores with metallic sulphides91
    Explanatory notes on the fusion93
    The effect of charcoal, flour, &c.94
    The effect of nitre95
    The effect of mineral sulphides95
        (3) Cupellation98
            The loss of silver101
            Condition affecting the loss102
            Methods of correction103
            Lead required for cupellation105
        (4) Calculation of the results in ounces to the ton of 2240 lbs. Table107
            Ores with metallic particles108
        (5) Explanatory notes110
        (6) Examples of dry silver assays113
    Wet assays116
        Gravimetric method117
        Gay-Lussac's method119
        Volhard's method121
        A modified Gay-Lussac123
        Volhard's method applied to arsenic124
Gold—Detection126
    Amalgamation assay126
    Dry assay127
        (1) Size of charges127
        (2) Sampling127
        (3) Assay tons131
        (4) Small buttons, weighing131
            "     "       measuring133
        (5) Concentration in lead136
            Quartz ores136
            Ores with oxide of iron138
            Ores with metallic sulphides139
        (6) Cyanide charges, residues, &c.140
        (7) Cupellation142
            Cupels142
            Cupellation temperature143
            Cupellation loss145
        (8) Inquartation146
        (9) Flatting149
        (10) Parting, in flasks151
                "         in test tubes152
                "         in glazed crucibles153
                "         Loss, &c.154
        (11) Check assays, surcharge154
        (12) Bullion assays in special apparatus156
            Silver, &c., in gold bullion157
        (13) Sampling of base bullion, &c.157
Cyanides—Commercial cyanides160
    Double cyanides161
    Prussic acid162
    Gold-dissolving power of cyanide liquor162
    Assay for cyanide strength163, 165
    Assay of commercial cyanide167
    Alkalinity of cyanides167
    Acidity of ores168
    Metals in cyanide liquors169
    Cyanicides169
Platinum170
Iridium171
Mercury171
    Dry assay172
    Wet method173
 
CHAPTER X.
COPPER, LEAD, THALLIUM, BISMUTH, ANTIMONY.
Copper—Introductory175
    Dry assay176
    Valuation of copper ores181
    Wet methods183
        (1) Electrolytic assay184
    Volumetric methods194
        (1) Cyanide method194
        (2) Iodide method199
        (3) Colorimetric method203
    Examination of commercial copper205
Lead211
    Dry assay211
    Wet assay213
        (1) Gravimetric method213
        (2) Volumetric method214
        (3) Colorimetric method218
Thallium219
Bismuth220
    Dry assay221
    Wet method221
        (1) Gravimetric determination222
        (2) Colorimetric assay223
Antimony225
    Dry assay225
    Wet method227
        (1) Gravimetric assay228
        (2) Volumetric method229
 
CHAPTER XI.
IRON, NICKEL, COBALT, ZINC, CADMIUM.
Iron231
    Gravimetric determination233
    Permanganate and bichromate methods234
    Stannous chloride method244
    Colorimetric determination247
Nickel251
    Dry assay251
    Electrolytic assay254
    Titration by cyanide255
Cobalt259
Zinc261
    Gravimetric method262
    Volumetric method263
    Gasometric method266
Cadmium269
 
CHAPTER XII.
TIN, TUNGSTEN, TITANIUM.
Tin271
    Vanning273
    Dry assay276
    Detection, &c.279
    Gravimetric determination281
    Volumetric determination282
    Examples284
Titanium292
Tungsten295
Niobic and Tantalic Oxides297
 
CHAPTER XIII.
MANGANESE, CHROMIUM, ETC.
Manganese298
    Gravimetric determination300
    Volumetric determination300
        Ferrous sulphate assay301
        Iodine assay302
    Colorimetric determination306
Chromium307
Vanadium310
Molybdenum311
Uranium312
 
CHAPTER XIV.
EARTHS, ALKALINE EARTHS, ALKALIES.
Alumina314
Thoria317
Zirconia317
Cerium318
Lanthanum and Didymium319
Yttria319
Beryllia319
Lime320
Strontia324
Baryta326
Magnesia328
The Alkalies330
    Sodium334
    Potassium336
    Lithium338
    Cæsium339
    Rubidium340
    Ammonium340
 
 
PART III.
 
CHAPTER XV.
OXYGEN AND OXIDES—THE HALOGENS.
Oxygen344
Oxides345
Water350
The Halogens358
    Chlorine359
    Bromine361
    Iodine362
    Fluorine363
 
CHAPTER XVI.
SULPHUR AND SULPHATES.
Sulphur367
    Gravimetric determination369
    Volumetric determination370
Sulphates377
Selenium379
Tellurium379
 
CHAPTER XVII.
ARSENIC, PHOSPHORUS, NITROGEN.
Arsenic381
    Gravimetric determination383
    Volumetric method, "iodine"384
            "          "         "uranic acetate"389
Phosphorus394
Gravimetric determination396
Volumetric determination397
Nitrogen and Nitrates400
 
CHAPTER XVIII.
SILICON, CARBON, BORON.
Silicon and Silicates405
Carbon and Carbonates414
Coals418
Shales420
Carbonates424
Boron and Borates429
 
APPENDIX A.
Table of atomic weights and other constants433
Table for converting degrees of the centigrade thermometer
    into degrees of Fahrenheit's scale435
Tables showing strengths of aqueous solutions of nitric and hydrochloric acids,
    of ammonia and of sulphuric acid436
 
APPENDIX B.
Estimation of small quantities of gold440
Practical notes on the iodide process of copper assaying441
Method of separating cobalt and nickel442
 
APPENDIX C.
A lecture on the theory of sampling444
 
 
Index450

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 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.