Sensitive Test for Silver and Halides - Analytical Chemistry (ACS

Ed. , 1945, 17 (4), pp 268–269. DOI: 10.1021/i560140a027. Publication Date: April 1945. ACS Legacy Archive. Note: In lieu of an abstract, this is th...
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Conversion of “Percentage Concentration” of E. M. BURDICK

AND

Mash

or Beer to Gallonage

JULIAN CORMAN

Agricultural Motor Fuels Division Northern Regional Research Laboratory, Peoria, 111.

I

S C O R R E L h T I S G laboratory and plant fermentation data involving concentrations of mash or fermented beer a t this laboratory, it is frequently necessary to convert so-called “percentage concentration” to gallonage. This requirement arises because different systems are commonly used to express concentrations in the laboratory and in the plant. . I n the laboratory i t is customary to express concentration on the basis of weight per volume, using metric units, while in the plant it is expressed as volume per weight, using English units. “Percentage concentration” is the weight, in grams, of original grains contained in 100 ml. of final slurry. “Gallonage” is t,lie volume,in U. S. gallons, of final slurry which contains one V. S. distillers’ bushel of original grains. Fhpressed mathematically,

the relationship between percellrage concentration and gallonage becomes: 56 X 453.59 X 100 = percentage concentration Gallonage X 3783 3 where 56 = pounds per U. S. diqtillers’ hu\hel of grain, 453 59 = grams per pound, and 3785 3 = nil. per U. S. gallon. From the above equation it can be seen that percentage concentration X gallonage = 671.04. Therefore, to change percentage concentration to gallonage or vice versa, it is only necessary to divide the constant (671.04) by whichever expression 1s given-for example, a 21 1% maqh or beer is equivalent to 671.04/21.1 = 31.8-gallon beer, or conversely a 31.Rgallon heer I $ equivalent to 671.04/31.8 = 21.1 % concentration.

Sensitive Test for Silver and the Halides PHILIP

S. BAKER AND J. H. REEDY

University of Illinois, Urbana,

SENSITIVENESS

W

HEX a solution of potassium iodide that has beensaturated with mercuric iodide is added to asilver chloride precipitate, a bright orange color is obtained. This reaction is very sensitive, anti has been m’ade tne basis for the following test for silver.

Since the test involves the separation of the silver as silver chloride ds a primary st,ep, the solubility of silver chloride is the limitiiig factor in the sensitiveness of the test. The effect of the concei1,tration of the iodide in the reagent is secondary in comparison. However, a high concentration of iodide is desirable, since it intensifies the color effect-that is, several drops of 0.1 M potassium iodomcrcurate may be required to give the same depth of color as a single drop of . I I potassium iodomercurate. I n general, the procedure will give a positive test for silver with a single drop of 0.001 J I silver nitrate using microtechnique. The sensitiveness thercfore approximates 5 micrograms of silver. Since the amount of silver chloride precipitate is the important factor, the sensitiveness of the test can be increased by concentrating the solution previous to the precipitation with hydrochloric acid.

PROCEDURE

.4 solution of potassium tetraiodomercurate is prc~purcd by shaking 24 grams of mercurir iodide with 100 ml. of warm molar potassium iodide solution. Upon standing, a small residue of mercuric iodide will remain undissolved and will settle to the bottom, leaving a saturated solution of the iodomercurate reagent. This solution is stable except for slight atmospheric oxidation, and in contact with mercuric iodide will undergo no noticeable change upon standing several months. The silver chloride is prepared as a suspension by adding a slight excess of dilute hydrochloric acid to silver nitrate. rlfter coagulation by warming and shaking, the precipitate is transferred to a small Kirsch funnel and washed thoroughly to remove any excess of chloride ions. The precipitate is aspirated to prartical dryness, and, after disconnecting from the vacuum, a drop of the iodomercurate solution is added, giving the orangered color. -4fe\v moments are allowed for the maximum color to develop. Thc color may be further intensified by drying the paper on a steam bath or in a drying oven. Prolonged hrnting must be avoidcd, since mercuric iodide is volatilg a t high temperatures. This procedure has been extended to include the detection of chloride and bromide by precipitating them with silver nitrate olution, and washing the precipitate until it is free from excess ,ilver ions. Silver in the form of silver iodide or silver sulfide cannot be detected in this way, since these salts are too insoluble t o react with the iodomercurate reagent. The test must be made without diluting the reagent, since dilution causes the separation of a red precipitate of mercuric iodide. This is due to the hydrolysis of the iodomercurate ion: Hg14-dilution Hg12 (red) 21-. One drop of water with 5 ml. of the reagent will produce a distinct red precipitate after standing 2 minutes, and a drop of the reagent with 10 ml. of water will ive a red precipitate in about the same time. I n order to avoif this interference, the silver halide is dried on the paper by aspiration.

+

Ill.

INTERFERENCES

Several ions interfere with this test for silver by forming yellow or red precipitates-.g., lead, mercurous, mercuric, bismuth, cupric, cadmium, stannic ions, and oxidizing agents in general. I n addition, alkaline solutions sometimes contain anions that form precipitates upon acidification--e.g., tungstate, thiosulfate, silicate, etc. With the exception of tungstic oxide, these precipitates give no colors with the reagent, but they may interfere by diluting the test. A411these interferences may be removed as follows:

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The solution is acidified with dilute nitric acid and warmed. Any precipitate of tungstic oxide, sulfur, silica, etc., is removed by filtration. The filtrate is then treated with dilute hydrochloric acid. If mercurous or lead ions may be present, chlorine solution or dilute nitric acid is added, and the mixture is t a r m e d . The precipitate is separated on a small paper in a Hirsch funnel and is washed with hot water as long as the washings show the presence of mercuric or lead ions. After the precipitate has been aspirated to dryness, a drop or two of the iodomercurate reagent is added. An orange precipitate indicates the presence of silver chloride.

Instead of the filtration technique, spot test or cone methods may be used. The necessary precaution against dilution of the reagent must be observed in both cases. Practically the same sensitiveness was found in all the methods used. 268

ANALYTICAL EDITION

A p d , 1945 NATURE

OF

THE PREClPlTATE

The orange color of the precipitate obtained in this test seems to be due to the presence of free mercuric iodide. This is shown by the fact t h a t this substance can be extracted from the precipitate by inert solvents--e.g., ethyl alcohol-leaving a yel-

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269

low residue. This free mercuric iodide may represent an excess of mercuric iodide dissolved in the reagent, but more probably comes from a decomposition of either the reagent or the silver precipitate. Further study of the composition and stability of the iodomercurates is planned.

Combination Gas-Delivery Tube and Stirrer ROBERT R. RUSSELL

AND

C A L V I N A. VANDERWERF

University of Kansas, Lawrence, Kanr.

THE

stirring device illustrated represents what the authors believe t o be the best method yet described for the rapid absorption, with efficient stirring, of gases in solid or heavy liquid suspensions, a common laboratory operation required by many varied types of reactions. Adaptation of the agitator itself as the gas-delivery tube is accomplished by the use of a glass tube stirrer shaft, A-A, which terminates a t the top as the inner tube of the revolving mercury seal, C. Gss-inlet tube B is clamped SO that the lower end dips a t least 8 cm. below the surface of the mercury. Either an ordinary mercury seal, H , or a liquid seal of the type described by Fieser (2)may be used for the flask. When properly aligned in the ball-bearing mountings (I?), D and E, E , the movable assembly turns freely and smoothly. Power is transmitted to the stirrer by means of the pulley, F, from the motor, G , set to one side. A suitable belt may be made by.twisting a heavy twine around itself four times, much as a grommet splice is made. T o prevent clogging, the direction of stirring should be away from the orifice. When the e n t i r e s e t u p is m o u n t e d o n one ring s t a n d i t is easily portable and can be weighed if desired. The apparatus is inexpensive and easily assembled. A d i s carded automobile generator bearing, available a t most junk yards, makes an excellent aligning ball-bearing, D, for the revolving mercury seal, C.

Little corrosion of the mercury was observed although, if the rotating seal is made sufficiently deep, other liquids may be employed as necessity demands. Modifications in the shape or orifice of the stirrer will be found superior in many other individual cases to which this device may be adapted. LITERATURE CITED

(1) Detoeuf, A., Bull. SOC. chim.,31, 102 (1922). (2) Fieser, L. F., "Experiments in Organic Chemistry", 2nd ed., pp. 309-10, New York, D. C. Heath and Co., 1941.

Use of Infrared H e a t in Determining A n i l i n e Points

k-

The authors found this device highly satisfactory for the chlorination of suspensions of urea and chalk in small amounts of water in the largescale synthesis of chlorourea ( 1 ) . Not only was the absorption time for the usual amount of chlorine reduced to one third of that required when the gas-inlet tube was independent of the stirrer, but it was also found that the chlorine absorption could easily be forced t o a point not reached during any reasonable length of time when a stationary gas-delivery tube was employed.

H A R O L D T. HOPKINS Standard Inspection Laboratory Standard Oil Development Company, Linden, N. J.

H

EATING by infrared radiation is particularly advantageous in the widely used aniline point test. The A.S.T.M. ( I ) version prescribes the alternate heating and cooling of 20 ml. of a mixture of equal parts of aniline and the product under test, in a glass-jacketed test tube equipped with a suitable stirrer. Heat is ordinarily supplied by the use of a liquid bath or a flame. The insulating effect of the glass air-jacket is troublesome during the heating periods, as the mixture is likely to be brought to an unnecessarily high temperature, thereby wasting time while the operator watches for the appearance of a cloud in the slowly cooling liquid. The substitution of an infrared heater for a liquid bath, or a flame, reduces lag to practically zero. The thermometer reading starts to go up or down almost immediately after turning the heat on or off. If an experienced operator keeps the liquid under close observation during the heating period, the range between minimum and maximum temperature need not exceed 3" C. Rate of heating can be regulated conveniently by changing the position of the infrared bulb. Protection of the apparatus from drafts is not necessary. An operator can cdnduct two simultaneous tests with ease, and there is an increase in safety and cleanliness. A further advantage is found in the fact that the tube may be vacuum-jacketed, which ensures a slow rate of cooling and improves the accuracy of the determination. The infrared heating devices used in the writer's laboratory are infrared lamps consisting of 260-watt bulbs with reflectors. They are inexpensive and easy to obtain. The working time consumed per test performed is reduced to less than two thirds that required when employing the older methods of heating. LITERATURE CITED (1) Am. SOC.Testing Materials, Aniline Point of Petroleum Products,

A.S.T.M. Serial Designation D611-43T.