An Introductory Course of Quantitative Chemical Analysis by Henry P. Talbot (good short books .TXT) 📖

The Project Gutenberg EBook of An Introductory Course of Quantitative Chemical Analysis, by Henry P. Talbot

This eBook is for the use of anyone anywhere at no cost and with almost no restrictions whatsoever. You may copy it, give it away or re-use it under the terms of the Project Gutenberg License included with this eBook or online at www.gutenberg.net

Title: An Introductory Course of Quantitative Chemical Analysis With Explanatory Notes

Author: Henry P. Talbot

Release Date: June 30, 2004 [EBook #12787]

Language: English

*** START OF THIS PROJECT GUTENBERG EBOOK QUANTITATIVE CHEMICAL ANALYSIS ***

Produced by Kevin Handy, Dave Maddock, Josephine Paolucci and the Online Distributed Proofreading Team.

[Transcriber's notes: In the chemical equations, superscripts are indicated with a ^ and subscripts are indicated with a . The affected item is enclosed in curly brackets {}. Examples are H^{+} for hydrogen ion and H{2}O for water. Since the underscore is already being used in this project, italics are designated by an exclamation point before and after the italicized word or phrase.]

AN INTRODUCTORY COURSE OF QUANTITATIVE CHEMICAL ANALYSIS WITH EXPLANATORY NOTES BY HENRY P. TALBOT PROFESSOR OF INORGANIC CHEMISTRY AT THE MASSACHUSETTS INSTITUTE OF TECHNOLOGY SIXTH EDITION, COMPLETELY REWRITTEN PREFACE

This Introductory Course of Quantitative Analysis has been prepared to meet the needs of students who are just entering upon the subject, after a course of qualitative analysis. It is primarily intended to enable the student to work successfully and intelligently without the necessity for a larger measure of personal assistance and supervision than can reasonably be given to each member of a large class. To this end the directions are given in such detail that there is very little opportunity for the student to go astray; but the manual is not, the author believes, on this account less adapted for use with small classes, where the instructor, by greater personal influence, can stimulate independent thought on the part of the pupil.

The method of presentation of the subject is that suggested by Professor A.A. Noyes' excellent manual of Qualitative Analysis. For each analysis the procedure is given in considerable detail, and this is accompanied by explanatory notes, which are believed to be sufficiently expanded to enable the student to understand fully the underlying reason for each step prescribed. The use of the book should, nevertheless, be supplemented by classroom instruction, mainly of the character of recitations, and the student should be taught to consult larger works. The general directions are intended to emphasize those matters upon which the beginner in quantitative analysis must bestow special care, and to offer helpful suggestions. The student can hardly be expected to appreciate the force of all the statements contained in these directions, or, indeed, to retain them all in the memory after a single reading; but the instructor, by frequent reference to special paragraphs, as suitable occasion presents itself, can soon render them familiar to the student.

The analyses selected for practice are those comprised in the first course of quantitative analysis at the Massachusetts Institute of Technology, and have been chosen, after an experience of years, as affording the best preparation for more advanced work, and as satisfactory types of gravimetric and volumetric methods. From the latter point of view, they also seem to furnish the best insight into quantitative analysis for those students who can devote but a limited time to the subject, and who may never extend their study beyond the field covered by this manual. The author has had opportunity to test the efficiency of the course for use with such students, and has found the results satisfactory.

In place of the usual custom of selecting simple salts as material for preliminary practice, it has been found advantageous to substitute, in most instances, approximately pure samples of appropriate minerals or industrial products. The difficulties are not greatly enhanced, while the student gains in practical experience.

The analytical procedures described in the following pages have been selected chiefly with reference to their usefulness in teaching the subject, and with the purpose of affording as wide a variety of processes as is practicable within an introductory course of this character. The scope of the manual precludes any extended attempt to indicate alternative procedures, except through general references to larger works on analytical chemistry. The author is indebted to the standard works for many suggestions for which it is impracticable to make specific acknowledgment; no considerable credit is claimed by him for originality of procedure.

For many years, as a matter of convenience, the classes for which this text was originally prepared were divided, one part beginning with gravimetric processes and the other with volumetric analyses. After a careful review of the experience thus gained the conclusion has been reached that volumetric analysis offers the better approach to the subject. Accordingly the arrangement of the present (the sixth) edition of this manual has been changed to introduce volumetric procedures first. Teachers who are familiar with earlier editions will, however, find that the order of presentation of the material under the various divisions is nearly the same as that previously followed, and those who may still prefer to begin the course of instruction with gravimetric processes will, it is believed, be able to follow that order without difficulty.

Procedures for the determination of sulphur in insoluble sulphates, for the determination of copper in copper ores by iodometric methods, for the determination of iron by permanganate in hydrochloric acid solutions, and for the standardization of potassium permanganate solutions using sodium oxalate as a standard, and of thiosulphate solutions using copper as a standard, have been added. The determination of silica in silicates decomposable by acids, as a separate procedure, has been omitted.

The explanatory notes have been rearranged to bring them into closer association with the procedures to which they relate. The number of problems has been considerably increased.

The author wishes to renew his expressions of appreciation of the kindly reception accorded the earlier editions of this manual. He has received helpful suggestions from so many of his colleagues within the Institute, and friends elsewhere, that his sense of obligation must be expressed to them collectively. He is under special obligations to Professor L.F. Hamilton for assistance in the preparation of the present edition.

HENRY P. TALBOT

!Massachusetts Institute of Technology, September, 1921!.

CONTENTS PART I. INTRODUCTION SUBDIVISIONS OF ANALYTICAL CHEMISTRY

GENERAL DIRECTIONS
  Accuracy and Economy of Time; Notebooks; Reagents; Wash-bottles;
  Transfer of Liquids

PART II. VOLUMETRIC ANALYSIS

GENERAL DISCUSSION
  Subdivisions; The Analytical Balance; Weights; Burettes;
  Calibration of Measuring Devices
GENERAL DIRECTIONS
  Standard and Normal Solutions

!I. Neutralization Methods!

ALKALIMETRY AND ACIDIMETRY
  Preparation and Standardization of Solutions; Indicators
STANDARDIZATION OF HYDROCHLORIC ACID
DETERMINATION OF TOTAL ALKALINE STRENGTH OF SODA ASH
DETERMINATION OF ACID STRENGTH OF OXALIC ACID

!II. Oxidation Processes!

GENERAL DISCUSSION BICHROMATE PROCESS FOR THE DETERMINATION OF IRON DETERMINATION OF IRON IN LIMONITE BY THE BICHROMATE PROCESS DETERMINATION OF CHROMIUM IN CHROME IRON ORE PERMANGANATE PROCESS FOR THE DETERMINATION OF IRON DETERMINATION OF IRON IN LIMONITE BY THE PERMANGANATE PROCESS DETERMINATION OF IRON IN LIMONITE BY THE ZIMMERMANN-REINHARDT PROCESS DETERMINATION OF THE OXIDIZING POWER OF PYROLUSITE IODIMETRY DETERMINATION OF COPPER IN ORES DETERMINATION OF ANTIMONY IN STIBNITE CHLORIMETRY DETERMINATION OF AVAILABLE CHLORINE IN BLEACHING POWDER

!III. Precipitation Methods!

DETERMINATION OF SILVER BY THE THIOCYANATE PROCESS PART III. GRAVIMETRIC ANALYSIS

GENERAL DIRECTIONS
  Precipitation; Funnels and Filters; Filtration and Washing of
  Precipitates; Desiccators; Crucibles and their Preparation
  for Use; Ignition of Precipitates
DETERMINATION OF CHLORINE IN SODIUM CHLORIDE
DETERMINATION OF IRON AND OF SULPHUR IN FERROUS AMMONIUM SULPHATE
DETERMINATION OF SULPHUR IN BARIUM SULPHATE
DETERMINATION OF PHOSPHORIC ANHYDRIDE IN APATITE
ANALYSIS OF LIMESTONE
  Determination of Moisture; Insoluble Matter and Silica; Ferric
  Oxide and Alumina; Calcium; Magnesium; Carbon Dioxide
ANALYSIS OF BRASS
  Electrolytic Separations; Determination of Lead, Copper, Iron
  and Zinc.
DETERMINATION OF SILICA IN SILICATES

PART IV. STOICHIOMETRY SOLUTIONS OF TYPICAL PROBLEMS PROBLEMS APPENDIX ELECTROLYTIC DISSOCIATION THEORY FOLDING OF A FILTER PAPER SAMPLE NOTEBOOK PAGES STRENGTH OF REAGENTS DENSITIES AND VOLUMES OF WATER CORRECTIONS FOR CHANGE OF TEMPERATURE OF STANDARD SOLUTIONS ATOMIC WEIGHTS LOGARITHM TABLES QUANTITATIVE CHEMICAL ANALYSIS PART I INTRODUCTION SUBDIVISIONS OF ANALYTICAL CHEMISTRY

A complete chemical analysis of a body of unknown composition involves the recognition of its component parts by the methods of !qualitative analysis!, and the determination of the proportions in which these components are present by the processes of !quantitative analysis!. A preliminary qualitative examination is generally indispensable, if intelligent and proper provisions are to be made for the separation of the various constituents under such conditions as will insure accurate quantitative estimations.

It is assumed that the operations of qualitative analysis are familiar to the student, who will find that the reactions made use of in quantitative processes are frequently the same as those employed in qualitative analyses with respect to both precipitation and systematic separation from interfering substances; but it should be noted that the conditions must now be regulated with greater care, and in such a manner as to insure the most complete separation possible. For example, in the qualitative detection of sulphates by precipitation as barium sulphate from acid solution it is not necessary, in most instances, to take into account the solubility of the sulphate in hydrochloric acid, while in the quantitative determination of sulphates by this reaction this solubility becomes an important consideration. The operations of qualitative analysis are, therefore, the more accurate the nearer they are made to conform to quantitative conditions.

The methods of quantitative analysis are subdivided, according to their nature, into those of !gravimetric analysis, volumetric analysis!, and !colorimetric analysis!. In !gravimetric! processes the constituent to be determined is sometimes isolated in elementary form, but more commonly in the form of some compound possessing a well-established and definite composition, which can be readily and completely separated, and weighed either directly or after ignition. From the weight of this substance and its known composition, the amount of the constituent in question is determined.

In !volumetric! analysis, instead of the final weighing of a definite body, a well-defined reaction is caused to take place, wherein the reagent is added from an apparatus so designed that the volume of the solution employed to complete the reaction can be accurately measured. The strength of this solution (and hence its value for the reaction in question) is accurately known, and the volume employed serves, therefore, as a measure of the substance acted upon. An example will make clear the distinction between these two types of analysis. The percentage of chlorine in a sample of sodium chloride may be determined by dissolving a weighed amount of the chloride in water and precipitating the chloride ions as silver chloride, which is then separated by filtration, ignited, and weighed (a !gravimetric! process); or the sodium chloride may be dissolved in water, and a solution of silver nitrate containing an accurately known amount of the silver salt in each cubic centimeter may be cautiously added from a measuring device called a burette until precipitation is complete, when the amount of chlorine may be calculated from the number of cubic centimeters of the silver nitrate solution involved in the reaction. This is a !volumetric! process, and is equivalent to weighing without the use of a balance.

Volumetric methods are generally more rapid, require less apparatus, and are frequently capable of greater accuracy than gravimetric methods. They are particularly useful when many determinations of the same sort are required.

In !colorimetric! analyses the substance to be determined is converted into some compound which imparts to its solutions a distinct color, the intensity of which must vary in direct proportion to the amount of the compound in the solution. Such solutions are compared with respect to depth of color with standard solutions containing known amounts of the colored compound, or of other similar color-producing substance which has been found acceptable as a color standard. Colorimetric methods are, in general, restricted to the determinations of very small quantities, since only in dilute solutions are accurate comparisons of color possible.

GENERAL DIRECTIONS

The following paragraphs should be read carefully and thoughtfully. A prime essential for success as an analyst is attention to details and the avoidance of all conditions which could destroy, or even lessen, confidence in the analyses when completed. The suggestions here given are the outcome of much experience, and their adoption will tend to insure permanently work of a high grade, while neglect of them will often lead to disappointment and loss of time.

ACCURACY AND ECONOMY OF TIME

The fundamental conception of quantitative analysis implies a necessity for all possible care in guarding against loss of material or the introduction of foreign matter. The laboratory desk, and all apparatus, should be scrupulously neat and clean at all times. A sponge should always be ready at hand, and desk and filter-stands should be kept dry and in good order. Funnels should never be allowed to drip upon the base of the stand. Glassware should always be wiped with