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of phosphorus pentoxide in the sample, and shake vigorously by hand. Mechanical shaking is of but slight advantage. The precipitate will settle out clear very quickly. Filter with suction through a 9 cm. filter-paper. Wash the precipitate free from acid with water, making no effort to remove the precipitate from the flask. The washing will take about two minutes. Test the filtrate by adding more ammonium molybdate solution and heating to 65° C. Transfer the precipitate and filter-paper to the Erlenmeyer flask, and run in standard alkali until the yellow precipitate is nearly dissolved. Shake to disintegrate the filter-paper. Now add I cc. phenolphthalein solution as indicator and continue adding the alkali cautiously until the pink color remains permanent for about a minute. The end-reaction is very sharp. In case an excess of alkali is added it can be titrated back with standard acid. Divide the burette reading by two and the result will be the per cent. of PO, in the sample.

Preparation of Reagents.

(a) Molybdic Solution: This solution is made as directed in Bulletin No. 46, Revised Edition, U. S. Department of Agriculture, Division of Chemistry, except that the solution is heated for five hours in a bath of water at a temperature of 65° to 67° C.

(b) Standard Potassium Hydroxide Solution: This is prepared by diluting 323.81 cc. of normal potassium hydroxide, free from carbonates, to I liter. One cc. is equal to I mg. phosphorus pentoxide.

(c) Standard Sulphuric Acid Solution: The strength of this solution is the same as that of the standard alkali.

(d) Phenolphthalein Solution: One gram of phenolphthalein is dissolved in 100 cc. of 50 per cent. alcohol. A. L. EMERY.

New Apparatus in Water Analysis.-In the June number of this Journal (p. 537) Messrs. Thomas and Hall describe under the above heading an apparatus for collecting samples of water for the determination of dissolved oxygen or carbon dioxide. While the apparatus may be a convenient one for this purpose, it seems a just criticism to point out that samples collected in this way will not represent the exact character of the water being tested and that, too, where results of the greatest accuracy possible are required. Suppose the sample is to be collected from the bottom of

a deep pond where the oxygen at most amounts to only a few
tenths per cent. of saturation. The entering water will come in
contact with the air in the bottle and will undoubtedly absorb
some oxygen.
It has been found in our work that when the dis-
solved oxygen content of the water is very low it is always neces-
sary to aspirate through the calibrated bottle at least several times
its volume of the water in order to be sure that the first portions
entering the bottle shall be completely displaced. In the apparatus
described no provision is made for this and it will be evident that
in such cases the results will not be accurate. The same criticism
will apply, though perhaps not with the same force, to determina-
tions of carbon dioxide made on samples collected in this way.
A. G. WOODMAN.

MASSACHUSETTS INSTITUTE OF TECHNOLOGY,
BOSTON, MASS, June 10, 1902.

NEW BOOKS.

GRUNDRISS DER QUALITATIVEN ANALYSE VOM STANDPUNKTE DER LEHRE VON DEN IONEN. BY DR. WILH. BÖTTGER. Leipsic. 1902. 250 pp. +15 pp. of tables.

This book may be briefly characterized as an interpretation in detail of the usual scheme of qualitative analysis with the help of the Laws of Chemical Equilibrium and the Ionic Theory. It differs from Ostwald's "Scientific Foundations of Analytical Chemistry" in the respect that the theoretical principles involved are gradually introduced in connection with the analytical procedure, instead of as an introduction to it; and in the respect that it is intended to serve as a working manual for a course of qualitative analysis, rather than as an accompaniment to such a course. It differs from the recent treatise of Treadwell on the same subject in that it is far less extensive and complete on the experimental side, and in that the theoretical interpretation of the reactions is given greater prominence. In fact, the point of view from which the book is written would seem to make it fitted to teach laws and theoretical principles with the help of qualitative analysis, rather than qualitative analysis with the help of the principles. And, correspondingly, for the training of exact analysts, the book can not be said to be fully satisfactory; for the conditions for securing

certainty and delicacy in the tests are often not sufficiently indicated. Moreover, the directions for laboratory experiments are either so incomplete or so interwoven with descriptions and theoretical explanations, that some difficulty would be met with in the use of the book as a laboratory manual. In spite, however, of these and other defects in the manner of presentation, the book is a very valuable contribution to the science, and well deserves the attention of students, and especially of teachers; of the subject; for it represents the first systematic attempt at a detailed interpretation of the reactions of qualitative analysis from the standpoint of modern theoretical chemistry, carried out by an author who shows himself to be thoroughly familiar with the principles involved.

To illustrate more fully the character of the book, the following summarized statement of its contents may be presented. After a very brief introduction, the author describes the precipitation and separation of lead, silver, and mercurous mercury; discusses incidentally filtration, washing, the significance of solubility and equilibrium in general; and presents the fundamental hypothesis of the Ionic Theory,-unfortunately in a somewhat intangible form, since, following the practice of Ostwald, the author avoids using the concepts of the Atomic Theory. He then describes and interprets the important additional reactions of these metals, introducing the subject of complex ions and their effects in increasing solubility in connection with the silver-ammonia and silvercyanogen compounds. The precipitation and separation of the metals of the hydrogen sulphide group are next described, theoretical explanations being interwoven with the procedure at each step. Incidentally, the Mass-Action Law in its general form is brought in, and is applied to the hydrogen sulphide precipitation. Additional reactions of the metals of the group are then discussed, and the varying degree of dissociation of different substances is referred to.

In

connecton with the succeeding groups of metals. a similar plan is followed. The principles relating to oxidation and reduction, to the precipitation by ammonia of alkaline-earth `phosphates, to hydrolysis, and to colloids, are treated under the aluminum and iron groups. Unfortunately, the solubility-product principle and the equilibrium-equation for dissolved electrolytes are not taken up till the calcium group is reached. By reason of

this fact the explanations of many points in the scheme of analysis for metals are so incomplete that much of the gain which should result from the application of the Ionic Theory is not realized.

The second part of the book is devoted to the detection and reactions of the acid radicals or anions. This part, consisting of sixty pages, is unusually thorough and complete. The dissociation-relations of the various acids, the subjects of catalysis and of fractional solution and crystallization, the principle of valence, and other theoretical considerations are introduced.

The third part of the book treats at length of the preliminary examination in the dry way, and of the methods of preparation of solutions for analysis. A number of special procedures adapted to the different insoluble substances are described.

A fourth part consisting of thirty-three pages, is devoted to the reactions of the rarer metals,-a subject too often neglected.

A set of tables, in the form of a separate pamphlet, summarizing the whole procedure, and intended for laboratory use, accompanies the book.

An English translation is in preparation, which will make this valuable work available for the use of elementary students.

ARTHUR A. NOYES.

H

THE JOURNAL

OF THE

AMERICAN CHEMICAL SOCIETY.

VOL. XXIV.-NO. 10.

OCTOBER, 1902.

WILLIAM A. NOYES, Editor, EDWARD HART, W. F. HILLEBRAND, J. H. LONG, WM. MCMURTRIE, ARTHUR A. NOYES, EDGAR F. SMITH, H. N. STOKES, H. P. TALBOT,

[blocks in formation]

A New Separation of Thorium from Cerium, Lanthanum, and Didym-
ium, and Its Application to the Analysis of Monazite. By Floyd
J. Metzger....

Action of Tellurium and Selenium on Gold and Silver Salts. By R. D.
Hall and Victor Lenher
The Application of Polarimetry to the Estimation of Tartaric Acid in
Commercial Products. By Edgar B. Kenrick and Frank B. Kenrick
The Equivalent Conductivity of the Hydrogen Ion Derived from
Transference Experiments with Hydrochloric Acid. By A. A.
Noyes and G. V. Sammet....

....

Some Preliminary Experiments upon the Clinkering of Portland
Cement. By E. D. Campbell.....

901

918

928

944

969

On the Quantitative Separation of Maltose and Lactose. By Charles I.
Boyden

993

On the Electrical Conductivity of Urine in Relation to Its Chemical
Composition. By J. H. Long..

The Retention of Arsenic by Iron in the Marsh-Berzelius Method. By
Charles Lathrop Parsons and Morris A. Stewart.

On the Constitution of Certain Organic Salts of Nickel and Cobalt as
They Exist in Aqueous Solution. By O. F. Tower..

On the Manganese Ferrocyanides. By Albert Ernest Dickie
NOTES: Note on the Preparation of Metallic Lithium; A Novel Con-
stant High Temperature Bath; On an Adulteration of Lavender
Oil with Salicylic Acid; The Production of Acylamines by the
Interaction of Sodium Salts of Monobasic Acids and Amine Hydro-
chlorides

.....

REVIEW OF AMERICAN CHEMICAL REsearch.

EASTON, PA.:

THE CHEMICAL PUBLISHING COMPANY.

...

996

1005

1012

1023

1024 437-480

Entered at the Post-office, Easton, Pa., as Second-class Matter

Everything intended for insertion in the Journal should be addressed to the Editor, William A. Noyes, Terre Haute, Ind. Orders for back numbers of the Journal should be addressed to the Librarian, É. G. Love, 108 West 55th Street, New York City. Changes of address should be sent to the Secretary, A. C. Hale, 352 A Hancock Street, Brooklyn, N. Y.

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