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A N T I M O N Y : ITS HISTORY, CHEMISTRY, MINERALOGY ...

A N T I M O N Y : ITS HISTORY, CHEMISTRY, MINERALOGY ...

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THE ANALYSIS OF ANTIMONY COMPOUNDS. 183<br />

and carbon bisulphide, (4) with alcohol alone, and (5) with ether.<br />

Dry the precipitate by warming it slightly. Remove as much<br />

precipitate as possible from the niter on to a watch-glass, and use<br />

hot ammonium sulphide to dissolve the remaining portion upon the<br />

filter-paper, which is then evaporated to dryness in a weighed crucible.<br />

The main part of the precipitate is then added to the crucible. Pass<br />

fuming nitric acid into the crucible covered with a watch-glass.<br />

After the first violent action is over, the crucible is heated in a<br />

water-bath until the evolution of gas has entirely ceased. Eemove<br />

the watch-glass and evaporate the contents of the crucible to dryness.<br />

In order to oxidise all the sulphur, this operation is repeated. The<br />

H2SO4 formed is eventually driven off by carefuj heating over a free<br />

flame. The open crucible is placed in the opening of an inclined<br />

disc of asbestos board, and the temperature is gradually increased<br />

until the full heat of the Teclu burner is obtained.<br />

(y) Estimation of Antimony in Native Sulphide of Antimony, according<br />

to Crookes.—The mineral is powdered, and 20 grains of it are<br />

taken. They are treated with a slight excess of HC1, and the mixture<br />

is gently heated until the H2S has completely evaporated. The<br />

solution is then filtered, and the filter is washed with dilute HCL<br />

The solution is then slowly evaporated in the flask until it is concentrated<br />

enough and freed from the excess of HCL The antimonv is<br />

now in the form of trichloride. A newly prepared solution of gallic<br />

acid is carefully added to a slight excess. Hot water is next added,<br />

and the precipitate of antimony bigallate is washed, dried, and<br />

weighed. The filtrate can be tested for iron, lead, copper, silver,<br />

arsenic, and, sometimes, zinc, cobalt and other metals remaining<br />

in solution. As iron is difficult of complete separation in the<br />

presence of gallic acid, other well-known methods are used for its<br />

determination.<br />

According to Mr L. Parry, the determination of antimony by the<br />

gravimetric method, especially if estimated as SbOo, is quite<br />

unreliable.<br />

(h) VoluTnetric.—(a) Mohr's Method*—Conversion of antimonious<br />

acid in alkaline solution into antimonic acid by iodine.<br />

Antimonious oxide, or any of its compounds, is dissolved in tartaric<br />

acid and water ; sodium carbonate is used to neutralise any excess of<br />

the acid used ; then a cold saturated solution of sodium bicarbonate<br />

is added in the proportion of 10 c.c. to about 0*1 gramme SboOs; to<br />

the clear solution starch is added, and ^ iodine until the blue colour<br />

appears. This operation must be done quickly, as when the bicar-<br />

* This is a useful method "when copper is absent..

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