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finely divided state it rapidly combines with oxygen, the compact metal requiring a strong heating to bring about this combination. It decomposes steam at a red heat, and slowly dissolves in dilute hydrochloric and sulphuric acids, but more readily in nitric acid. Cobalt burns in nitric oxide at 150 deg. C. giving the monoxide. It may be obtained in the pure state, according to C. Winkler (_Zeit. fur anorg. Chem._, 1895, 8, p. 1), by electrolysing the pure sulphate in the presence of ammonium sulphate and ammonia, using platinum electrodes, any occluded oxygen in the deposited metal being removed by heating in a current of hydrogen. Three characteristic oxides of cobalt are known, the monoxide, CoO, the sesquioxide, Co2O3, and tricobalt tetroxide, Co3O4; besides these there are probably oxides of composition CoO2, Co8O9, Co6O7 and Co4O5. Cobalt monoxide, CoO, is prepared by heating the hydroxide or carbonate in a current of air, or by heating the oxide Co3O4 in a current of carbon dioxide. It is a brown coloured powder which is stable in air, but gives a higher oxide when heated. On heating in hydrogen, ammonia or carbon monoxide, or with carbon or sodium, it is reduced to the metallic state. It is readily soluble in warm dilute mineral acids forming cobaltous salts. Cobaltous hydroxide, Co(OH)2, is formed when a cobaltous salt is precipitated by caustic potash in the absence of air. A blue basic salt is precipitated first, which, on boiling, rapidly changes to the rose-coloured hydroxide. It dissolves in acids forming cobaltous salts, and on exposure to air it rapidly absorbs oxygen, turning brown in colour. A. de Schulten (_Comptes Rendus_, 1889, 109, p. 266) has obtained it in a crystalline form; the crystals have a specific gravity of 3.597, and are easily soluble in warm ammonium chloride solution. Cobalt sesquioxide, Co2O3, remains as a dark-brown powder when cobalt nitrate is gently heated. Heated at 190-300 deg. in a current of hydrogen it gives the oxide Co3O4, while at higher temperatures the monoxide is formed, and ultimately cobalt is obtained. Cobaltic hydroxide, Co(OH)3, is formed when a cobalt salt is precipitated by an alkaline hypochlorite, or on passing chlorine through water containing suspended cobaltous hydroxide or carbonate. It is a brown-black powder soluble in hydrochloric acid, chlorine being simultaneously liberated. This hydroxide is solubl
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