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atomic See also:weight 190.9 See also:OSMIUM [See also:symbol Os. (0= r6)] , in See also:chemistry, a metallic See also:element, found in See also:platinum ore in small particles, consisting essentially of an alloy of See also:osmium and See also:iridium and known as osmiridium . It was first obtained in 1803 by See also:Smithson See also:Tennant (Phil . Trans., 1804, 94, p . 411) . It may be prepared from osmiridium by fusing the alloy with See also:zinc, the zinc being afterwards removed by See also:distillation . T e See also:residue so obtained is then powdered and ignited with bariu nitrate, which converts the iridium into its See also:oxide and the osmium into See also:barium osmiate . The barium See also:salt is extracted by See also:water and boiled with nitric See also:acid, when the osmium volatilizes in the See also:form of its tetroxide . As an alternative the osmiridium is fused with zinc, the See also:regulus treated with hydrochloric acid, and then heated with barium nitrate and barium peroxide . After See also:fusion, the See also:mass is finely powdered and treated with See also:cold dilute hydrochloric acid; and when See also:action has finished, nitric and sulphuric acids are added, the precipitated barium sulphate removed, the liquid distilled and the osmium precipitated as sulphide . The sulphide is converted into See also:sodium osmichloride by fusion with salt, in a current of See also:chlorine, the sodium salt transformed into ammonium salt by precipitation with ammonium chloride, and the ammonium salt finally heated strongly (H . Sainte-Claire-Deville and H . J . Debray, An. See also:min., 1859 [5], 16, 74; see also C . E . Claus, Jour. prakt . Chem., 1862, 85, p . 142; F . See also:Wohler, Pogg . 31, p . 161; E . Leidie and L . Quenessen, See also:Bull. See also:soc. aim., 1903 (8), 29, p . 801) . The tetroxide, OsO4, can be easily reduced to the See also:metal by dissolving it in hydrochloric acid and adding zinc, See also:mercury, or an alkaline formate to the liquid, or by passing its vapour, mixed with See also:carbon dioxide and monoxide, through a red-hot See also:porcelain See also:tube . The metal has a See also:blue-See also:grey See also:colour, and may be obtained in the crystalline See also:state by See also:solution in See also:tin . Its specific gravity is 21.3-22.48 (Deville and Debray) and its specific See also:heat is o•03113 (See also:Regnault) . It can be distilled in the electric See also:furnace . In the massive state it is insoluble in all acids, but when freshly precipitated from solutions it dissolves in fuming nitric acid . On fusion with See also:caustic potash it yields See also:potassium osmiate . It combines with See also:fluorine at See also:roc° C., and when heated with chlorine it forms a mixture of chlorides . A colloidal variety was obtained by A . Gutbier and G . Hofmeier (Jour. prakt . Chem., 1905 (2), 71, p . 452) by reducing osmium compounds with See also:hydrazine See also:hydrate in the presence of See also:gum arabic . Several oxides of osmium are known . The protoxide, OsO, is obtained as a dark grey insoluble See also:powder when osmium sulphite is heated with sodium carbonate in a current of carbon dioxide . The sesquioxide, OS20,, results on See also:heating osmium with an excess of the tetroxide . The dioxide, OsO2, is formed when potassium osmichloride is heated with sodium carbonate in a current of carbon dioxide, or by See also:electrolysis of a solution of the tetroxide in the presence of See also:alkali . It is insoluble in acids and exists in several hydrated forms . The osmiates, corresponding to the unknown trioxide OsO3, are red or See also:green coloured salts; the solutions are only See also:stable in the presence of excess of caustic alkali; on boiling an aqueous solution of the potassium salt it decomposes readily, forming a See also:black precipitate of osmic acid, H20s04 . Potassium osmiate, K20sO42H2O, formed when an alkaline solution of the tetroxide is decomposed by See also:alcohol, or by potassium nitrite, crystallizes in red octahedra . It is stable in dry See also:air, but in moist air rapidly decomposes . The tetroxide, OsO4, is formed when osmium compounds are heated in air, or with aqua regia, or fused with caustic alkali and See also:nitre . It is obtained as a yellowish coloured mass and can be sublimed in the form of needles which melt at 4o° C . It possesses an unpleasant See also:smell and its vapour is extremely poisonous . It dissolves slowly in water, and the aqueous solution is reduced by most metals with precipitation of osmium . It acts as an oxidizing See also:agent, liberating See also:iodine from potassium iodide, converting alcohol into acetaldehyde, &c . Osmium dichloride, OsC12, is obtained as a dark coloured powder when the metal is heated in a current of chlorine . Its solution in water is deep blue in colour, but the colour changes rapidly togreen and yellow . The trichloride, OsC18, is only known in solution and is formed by the reducing action of mercury on See also:ammonia-cal solutions of the tetroxide . A hydrated form of See also:composition OsC12.3H2O has been described . The tetrachloride, OsC14, is obtained as a dark red sublimate (mixed with the dichloride) when osmium is heated in dry chlorine . It is soluble in water, but the dilute solution readily decomposes on See also:standing . It combines with the chlorides of the alkali metals to form characteristic See also:double salts of the type OsC14.2MCl (osmichlorides) . Potassium osmichloride, K2OsCl,, is formed when a mixture of osmium and potassium chloride is heated in a current of chlorine, or on adding potassium chloride and e lcohol to a solution of the tetroxide in hydrochloric acid . It crystallizes in dark red octahedra which are almost insoluble in cold water . The aqueous solution decomposes rapidly on boiling . Iodine has no action on osmium, but on warming the tetroxide with a mixture of potassium iodide and hydrochloric acid a deep See also:emerald green colour is produced, due to the formation of a See also:compound OsI2.2HI; this reaction is a delicate test for osmium (E . Pinerua See also:Alvarez, Comptes rendus, 1905, 140, p .
1254)
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Osmium disulphide, OsS2, is obtained as a dark See also: |
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