The higher sulphides of the arsenic group, and arsenious and antimonious sulphides among the lower ones, combine with the alkali sulphides to form soluble alkali salts of sulpho-acids, in the same way as carbon bisulphide does. In the case of arsenious sulphide, for instance, we have the action
As2S3 + (NH4)2S ⇄ 2 NH4AsS2.
(4)
The salt, ammonium sulpharsenite, is ionized as follows:
NH4AsS2 ⇄ NH4+ + AsS2−.
Sulpho-Acids.
2 HAsS2 ⥂ As2 S3 ↓ + H2S ↑.
This instability of the sulpho-acids is entirely analogous to the instability of the metal hydrosulphides (p. [203]) and to the instability of certain oxygen acids, notably of carbonic acid. Sulpho-carbonic acid, H2CS3, is the best-known free acid of this type. It may be precipitated, undecomposed, as an oil, and its gradual decomposition into hydrogen sulphide and carbon disulphide may be observed.