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Ch. 2: Platinum in 1916

Ch. 2: Platinum in 1916 Page of 78 Ch. 2: Platinum in 1916 Text size:minus plus Restore normal size   Mail page  Print this page
PLATINUM AND ALLIED METALS.                                 19
these metals, as they are soluble in dilute nitric acids; crude platinum can be dissolved only in concentrated aqua regia, a mixture of 3 parts of hydrochloric (muriatic) acid and 1 part of nitric acid.
In some placer deposits the grains of platinum are coated with a dark film and somewhat resemble the grains of the dark minerals chromite, magnetite, or ilmenite, from which they are separated by careful panning, as the specific gravity of platinum is greater than that of any of those minerals.
Platinum will not amalgamate with quicksilver alone, but will amalgamate if sodium is added. In ordinary quicksilver amalga­mation the flakes of platinum float on the surface and can be removed. If sodium amalgam is used, the platinum may be separated from gold by agitating the amalgam with water until all the sodium is used up to form sodium hydroxide; then the platinum will come out on the surface of the amalgam, provided, of course, the amalgam is suffi­ciently liquid.
Platinum has a hardness of 4 to 5, and can be scratched with a knife. It is so malleable that it can be pounded without heating into very thin sheets. It is practically infusible; the grains can not be melted together, as particles of gold can.
A relatively simple chemical test can be made to determine the platinum. The metallic particles are dissolved by boiling in con­centrated aqua regia and the resulting solution is allowed to remain on the stove till dry. The residue is dissolved again in hydrochloric acid and evaporated by boiling till the solution is thick but not quite dry. This mass is dissolved in distilled water and a few drops of sul­phuric acid and of potassium iodide solution are added, which, in the presence of platinum, causes the solution to turn a very character­istic wine-red, if much of the metal is present, or to a reddish pink in thepresence of small quantities of platinum.
The test outlined above is fairly delicate, but it can not be used to detect traces of platinum in the presence of large quantities of iron or other elements.
A second test may be applied to the aqua regia solution after the resolution in hydrochloric acid outlined above. In this test potas­sium chloride (KC1) is added to the solution, which precipitates yellow crystals of potassium platinic chloride (K2PC1„), if platinum is present.
A third test may be applied. Add ammonium chloride (NH4C1) to the aqua regia solution, which will precipitate yellow crystals of ammonium platinic chloride, if platinum is present.
The precipitates from tests 2 and 3 are both insoluble in alcohol but are soluble in water and may be reduced to platinum sponge by heating.
All these tests are comparatively simple and positive when made on single grains, but they can not be rehed upon when various other elements are present in the material tested. It is, therefore, recom­mended that their use be restricted to grains of a single mineral picked from the concentrates obtained by panning a sample of either rock or gravel.
Ch. 2: Platinum in 1916 Page of 78 Ch. 2: Platinum in 1916
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US Geol. Surv. 1916. Gemstones, Metals.
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