One part of calcium sulphate at the ordinary temperature requires about 500 parts of water for solution, strontium sulphate about 7,000 parts, barium sulphate about 400,000 parts, whilst beryllium sulphate is easily soluble in water.
We refer beryllium to the class of the bivalent metals of the alkaline earths—that is, we ascribe to its oxide the formula BeO, and do not consider it as trivalent (Be = 13·5, Chapter VII., Note 445), although that view has been upheld by many chemists. The true atomic composition of beryllium oxide was first given by the Russian chemist, Avdéeff (1819), in his researches on the compounds of this metal. He compared the compounds of beryllium to those of magnesium, and refuted the notion prevalent at the time, of the resemblance between the oxides of beryllium and aluminium, by proving that beryllium sulphate presents a greater resemblance to magnesium sulphate than to aluminium sulphate. It was especially noticed that the analogues of alumina give alums, whilst beryllium oxide, although it is a feeble base, easily giving, like magnesia, basic and double salts, does not form true alums. The establishment of the periodic system of the elements (1869), considered in the following chapter, immediately indicated that Avdéeff's view corresponded with the truth—that is, that beryllium is bivalent, which therefore necessitated the denial of its trivalency.
This scientific controversy resulted in a long series of researches (1870–80) concerning this element, and ended in Nilson and Pettersson—two of the chief advocates of the trivalency of beryllium—determining the vapour density of BeCl2 = 40, (Chapter VII., Note 445), which gave an undoubted proof of its bivalency (see also Note 835).
Beryllium oxide, like aluminium oxide, is precipitated from solutions of its salts by alkalis as a gelatinous hydroxide, BeH2O2, which, like alumina, is soluble in an excess of caustic potash or soda. This reaction may be taken advantage of for distinguishing and separating beryllium from aluminium, because when the alkaline solution is diluted with water and boiled, beryllium hydroxide is precipitated, whilst the alumina remains in solution. The solubility of the beryllium oxide at once clearly indicates its feeble basic properties, and, as it were, separates this oxide from the class of the alkaline earths. But on arranging the oxides of the above-described metals of the alkaline earths according to their decreasing atomic weights we have the series BaO, SrO, CaO, MgO, BeO, in which the basic properties and solubility of the oxides consecutively and distinctly decrease until we reach a point when, had we not known of the existence of the beryllium oxide, we should expect to find in its place an oxide insoluble in water and of feeble basic properties. If an alcoholic solution of caustic potash be saturated with the hydrate of BeO, and evaporated under the receiver of an air pump, it forms silky crystals BeK2O2.