It is readily soluble in warm dilute mineral acids forming cobaltous salts.
Cobaltous hydroxide, Co(OH) 21 is formed when a cobaltous salt is precipitated by caustic potash in the absence of air.
It dissolves in acids forming cobaltous salts, and on exposure to air it rapidly absorbs oxygen, turning brown in colour.
Cobaltic hydroxide, Co(OH) 31 is formed when a cobalt salt is precipitated by an alkaline hypochlorite, or on passing chlorine through water containing suspended cobaltous hydroxide or carbonate.
Cobalt dioxide, Co02, has not yet been isolated in the pure state; it is probably formed when iodine and caustic soda are added to a solution of a cobaltous salt.
By suspending cobaltous hydroxide in water and adding hydrogen peroxide, a strongly acid liquid is obtained (after filtering) which probably contains cobaltous acid, H2CoO 3.
The cobaltous salts are formed when the metal, cobaltous oxide, hydroxide or carbonate, are dissolved in acids, or, in the case of the insoluble salts, by precipitation.
For the action of ammonia on the cobaltous salts in the presence of air see Cobaltammines (below).
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.
It may be prepared in the amorphous form by heating cobalt with sulphur dioxide, in a sealed tube, at 200° 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).
Cobaltous sulphate, CoSO 4.7H 2 O, is found naturally as the mineral bieberite, and is formed when cobalt, cobaltous oxide or carbonate are dissolved in dilute sulphuric acid.
The ammonium cobalto-cobaltisulphite is prepared by saturating an air-oxidized ammoniacal solution of cobaltous chloride with sulphur dioxide.
Cobaltous cyanide, Co(CN)2.3H20, is obtained when the carbonate is dissolved in hydrocyanic acid or when the acetate is precipitated by potassium cyanide.
The hexammine salts are formed by the oxidizing action of air on dilute ammoniacal solutions of cobaltous salts, especially in presence of a large excess of ammonium chloride.
They are formed by the action of nitrous fumes on ammoniacal solutions of cobaltous salts, or purpureo-salts, or by the mutual reaction of chlorpurpureosalts and alkaline nitrites.