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CoCl2.2H2O and CoCl2 . 4H2O have been described (P. Sabatier, _Bull. Soc. Chim._ 51, p. 88; Bersch, _Jahresb. d. Chemie_, 1867, p. 291). Double chlorides of composition CoCl2.NH4Cl.6H2O; CoCl2.SnCl4.6H2O and CoCl2.2CdCl2.12H2O are also known. By the addition of excess of ammonia to a cobalt chloride solution in absence of air, a greenish-blue precipitate is obtained which, on heating, dissolves in the solution, giving a rose-red liquid. This solution, on standing, deposits octahedra of the composition CoCl2.6NH3. These crystals when heated to 120 deg. C. lose ammonia and are converted into the compound CoCl2.2NH3 (E. Fremy). The bromide, CoBr2, resembles the chloride, and may be prepared by similar methods. The hydrated salt readily loses water on heating, forming at 100 deg. C. the hydrate CoBr2.2H2O, and at 130 deg. C. passing into the anhydrous form. The iodide, CoI2, is produced by heating cobalt and iodine together, and forms a greyish-green mass which dissolves readily in water forming a red solution. On evaporating this solution the hydrated salt CoI2.6H2O is obtained in hexagonal prisms. It behaves in an analogous manner to CoBr2.6H2O on heating. Cobalt fluoride, CoF2.2H2O, is formed when cobalt carbonate is evaporated with an excess of aqueous hydrofluoric acid, separating in rose-red crystalline crusts. Electrolysis of a solution in hydrofluoric acid gives cobaltic fluoride, CoF3. Sulphides of cobalt of composition Co4S3, CoS, Co3S4, Co2S3 and CoS2 are known. The most common of these sulphides is cobaltous sulphide, CoS, which occurs naturally as syepoorite, and can be artificially prepared by heating cobaltous oxide with sulphur, or by fusing anhydrous cobalt sulphate with barium sulphide and common salt. By either of these methods, it is obtained in the form of bronze-coloured crystals. It may be prepared in the amorphous form by heating cobalt with sulphur dioxide, in a sealed tube, at 200 deg. C. In the hydrated condition it is formed by the action of alkaline sulphides on cobaltous salts, or by precipitating cobalt acetate with sulphuretted hydrogen (in the absence of free acetic acid). It is a black amorphous powder soluble in concentrated sulphuric and hydrochloric acids, and when in the moist state readily oxidizes on exposure. Cobaltous sulphate, CoSO4.7H2O, is found naturally as the mineral bieberite, and is formed when
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