in the mixture; for the oxalate of lime or magnesia in the second case is converted into oxalate of potass.
Add now the solution of acetate of lead to the fluid as long as any precipitate is formed. Collect the precipitate on a filter, wash it well, and dry it by compression between folds of bibulous paper. Remove this precipitate, which consists of oxalate of lead and organic matter in union with oxide of lead, and rub it up very carefully while damp with a little water in a mortar. Transmit sulphuretted hydrogen gas briskly for an hour, so that the whole white precipitate shall be thoroughly blackened; filter and boil. In this manner is formed a sulphuret of lead, which retains a great deal of animal matter; and the oxalic acid being set free, is found in the solution tolerably pure. Filtration before boiling is an essential point in this step, to prevent animal matter being dissolved by the water from the sulphuret of lead. More animal matter may still be separated by evaporating the liquid to dryness at 212°, keeping it at that temperature for a few minutes, and re-dissolving and filtering. The solution will now exhibit the properties of oxalic acid.
I have found that when this process was applied to a decoction of an ounce of beef in six ounces of water, with which one grain of anhydrous oxalic acid had been mixed, all the tests acted characteristically on the solution ultimately procured. I have farther found, that when two grains of oxalate of lime, which correspond with one grain of oxalic acid, were mixed with a similar decoction in which some fragments of beef were purposely left to complicate the process, a solution was eventually obtained, which gave with muriate of lime a white precipitate insoluble in a little muriatic acid, with sulphate of copper a greenish-white precipitate also insoluble in a little muriatic acid, and with nitrate of silver a white precipitate which fulminated and was almost all dispersed, but left a little charcoal, owing to its containing a small proportion of animal matter. In a case which lately happened in London, every test acted as here described, except that the oxalate of lime did not fulminate, owing to the presence of organic impurities.[1] In order to try the test of fulmination in such circumstances, it is essential to dry the precipitated oxalate of silver thoroughly before raising the temperature to the point at which fulmination usually occurs.
The process now recommended is both delicate and accurate. An objection has been advanced against it,—that acetate of lead will throw down chloride of lead as well as the oxalate of lead; that both will subsequently be decomposed by the sulphuretted-hydrogen? and that the hydrochloric acid thus brought into the solution with the oxalic acid will be precipitated by the nitrate of silver, and form a mixture of salts which will not fulminate characteristically.[2] This objection is not well founded. Chloride of lead being soluble in thirty parts of temperate water, it will seldom be thrown down from such fluids as occur in medico-legal inquiries; and besides it is easily removed, as I have ascertained, by washing the precipitate with moderate care on the filter.
