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e smell. In its general behaviour it resembles arsine, burning with a violet flame and being decomposed by heat into its constituent elements. When passed into silver nitrate solution it gives a black precipitate of silver antimonide, SbAg3. It is decomposed by the halogen elements and also by sulphuretted hydrogen. All three hydrogen atoms are replaceable by organic radicals and the resulting compounds combine with compounds of the type RCl, RBr and RI to form stibonium compounds. There are three known oxides of antimony, the trioxide Sb4O6 which is capable of combining with both acids and bases to form salts, the tetroxide Sb2O4 and the pentoxide Sb2O5. Antimony trioxide occurs as the minerals valentinite and senarmontite, and can be artificially prepared by burning antimony in air; by heating the metal in steam to a bright red heat; by oxidizing melted antimony with litharge; by decomposing antimony trichloride with an aqueous solution of sodium carbonate, or by the action of dilute nitric acid on the metal. It is a white powder, almost insoluble in water, and when volatilized, condenses in two crystalline forms, either octahedral or prismatic. It is insoluble in sulphuric and nitric acids, but is readily soluble in hydrochloric and tartaric acids and in solutions of the caustic alkalies. On strongly heating in air it is converted into the tetroxide. The corresponding hydroxide, orthoantimonious acid, Sb(OH)3, can be obtained in a somewhat impure form by precipitating tartar emetic with dilute sulphuric acid; or better by decomposing antimonyl tartaric acid with sulphuric acid and drying the precipitated white powder at 100 deg. C. Antimony tetroxide is formed by strongly heating either the trioxide or pentoxide. It is a nonvolatile white powder, and has a specific gravity of 6.6952; it is insoluble in water and almost so in acids--concentrated hydrochloric acid dissolving a small quantity. It is decomposed by a hot solution of potassium bitartrate. Antimony pentoxide is obtained by repeatedly evaporating antimony with nitric acid and heating the resulting antimonic acid to a temperature not above 275 deg. C.; by heating antimony with red mercuric oxide until the mass becomes yellow (J. Berzelius); or by evaporating antimony trichloride to dryness with nitric acid. It is a pale yellow powder (of specific gravity 6.5), which on being heated strongly gives up o
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