According to MacColeb, gypsum dehydrated at 200° has a specific gravity 2·577, and heated to its point of fusion, 2·654. Potilitzin (1894) also admits the two above-named modifications of anhydrous gypsum, which, moreover, always contain the semi-hydrated hydrate (Note 876), and he explains by their relation to water the phenomena observed in the solidification of a mixture of burnt gypsum and water.
As Marignac showed, gypsum, especially when desiccated at 120°, easily gives supersaturated solutions with respect to CaSO4,2H2O, which contain as much as 1 part of CaSO4 to 110 parts of water. Boiling dilute hydrochloric acid dissolves gypsum, forming calcium chloride. The behaviour of gypsum towards the alkaline carbonates has been described in Chapter X. Alcohol precipitates gypsum from its aqueous solutions, because, like the sulphates in general, it is sparingly soluble in alcohol. Gypsum, like all the sulphates, when heated with charcoal, gives up its oxygen, forming the sulphide, CaS. Calcium sulphate, like magnesium sulphate, is capable of forming double salts, but with difficulty, and they are chemically less stable. They contain, as is always the case with double salts, less water of crystallisation than the component salts. Rose, Struvé, and others obtained the salt CaK2(SO4)2,H2O; a mixture of gypsum with an equivalent amount of potassium sulphate and water solidifies into a homogeneous mass. Fritzsche obtained the corresponding sodium salt in a hydrated and anhydrous state, by heating a mixture of gypsum with a saturated solution of sodium sulphate. The anhydrous salt occurs in nature as glauberite.
Fritzsche also obtained gaylussite, Na2Ca(CO3)2,5H2O, by pouring a saturated solution of sodium carbonate on to freshly-precipitated calcium carbonate. Calcium also forms basic salts, but only a few. Veeren (1892) obtained Ca(NO3)2Ca(OH)2,2½H2O by leaving powdered caustic lime in a saturated solution of Ca(NO3)2 until it solidified. This salt is decomposed by water.