A colloidal selenium was obtained by C. Paal and C. Koch (Ber., 1905, 38, p. 526) by reducing selenious acid dissolved in an aqueous solution of sodium protalbate with hydrazine hydrate and hydrochloric acid, the precipitate obtained being then dissolved in sodium carbonate.
In this process, the residues are boiled with a dilute sulphuric acid to which nitric acid and potassium chlorate are added in order to transform the element into selenic acid, H 2 Se0 4, which is then reduced to selenious acid, H 2 Se0 3, by boiling with hydrochloric acid, and finally to selenium by sulphur dioxide.
Selenious acid, H 2 SeO 3, is obtained in the crystalline form when a solution of selenium dioxide in water is concentrated over sulphuric acid.
The amorphous variety, which only differs from the vitreous form in its state of aggregation, is obtained by reducing solutions of selenious acid with sulphur dioxide.