DETERMINATION OF BISMUTH.
This separation presents considerable difficulty, because the metal is not precipitated as a compact mass on the platinum. The bismuth is always obtained in the same form, no matter whether it is precipitated from an acid solution, or from the double ammonium oxalate, or, finally, from a solution to which potassium tartrate has been added. As large a surface as possible must be used, and the dish piled to the rim; then, if the quantity of bismuth is small, the washing with water, alcohol, and ether may be effected without any loss of the element. If small quantities of the metal separate from the dish, they must be collected on a tared filter, and determined separately. In our experiments, an excess of ammonium oxalate was added to a nitric acid solution of bismuth. During the electrolytic decomposition, a separation of the peroxide was observed at the positive electrode, which, however, slowly disappeared. In order to prevent the reduced metal from oxidation, the last traces of water are completely removed by repeated washings with alcohol and anhydrous ether.