From one ton of residue 10 to 20 kilogrms. of crude sulphates are obtained, the activity of which is from thirty to sixty times as great as that of metallic uranium. They must now be purified. For this purpose they are boiled with sodium carbonate and transformed into the chlorides. The solution is treated with sulphuretted hydrogen, which gives a small quantity of active sulphides containing polonium. The solution is filtered, oxidised by means of chlorine, and precipitated with pure ammonia. The precipitated hydrates and oxides are very active, and the activity is due to actinium. The filtered solution is precipitated with sodium carbonate. The precipitated carbonates of the alkaline earths are washed and converted into chlorides. These chlorides are evaporated to dryness, and washed with pure concentrated hydrochloric acid. Calcium chloride dissolves almost entirely, whilst the chloride of barium and radium remains insoluble. Thus, from one ton of the original material about 8 kilogrms. of barium and radium chloride are obtained, of which the activity is about sixty times that of metallic uranium. The chloride is now ready for fractionation.
As I said above, by passing sulphuretted hydrogen through the various hydrochloric acid solutions obtained during the course of the process, active sulphides are precipitated, of which the activity is due to polonium. These sulphides chiefly contain bismuth, a little copper and lead; the latter metal occurs in relatively small amount, because it has been to a great extent removed by the soda solution, and because its chloride is only slightly soluble. Antimony and arsenic are found among the oxides only in the minutest quantity, their oxides having been dissolved by the soda. In order to obtain the very active sulphides, the following process was employed:—The solutions made strongly acid with hydrochloric acid were precipitated with sulphuretted hydrogen; the sulphides thus precipitated are very active, and are employed for the preparation of polonium; there remain in the solution substances not completely precipitated in presence of excess of hydrochloric acid (bismuth, lead, antimony). To complete the precipitation, the solution is diluted with water, and treated again with sulphuretted hydrogen, which gives a second precipitate of sulphides, much less active than the first, and which have generally been rejected. For the further purification of the sulphides, they are washed with ammonium sulphide, which removes the last remaining traces of antimony and arsenic. They are then washed with water and ammonium nitrate, and treated with dilute nitric acid. Complete solution never occurs; there is always an insoluble residue, more or less considerable, which can be treated afresh if it is judged expedient. The solution is reduced to a small volume and precipitated either by ammonia or by excess of water. In both cases the lead and the copper remain in solution; in the second case, a little bismuth, scarcely active at all, remains also in solution.