The above process possesses the undeniable advantage of completely destroying the organic substances, at the same time avoiding the introduction of sulphate of potassa, the presence of which impairs the usefulness of the preceding method; but it necessitates the presence of numerous foreign bodies in the substance to be analysed, and this should be avoided. The absolute purity of reagents is not always to be attained, and the results of an analysis are the more certain, in proportion as they are less numerous and more easily purified.
BY MEANS OF POTASSA AND NITRIC ACID.
It has been proposed, instead of using nitrate of lime, to dissolve the organic matter in potassa and then saturate the fluid with nitric acid. This method is evidently more complicated than the simple treatment with nitrate of potassa, and possesses, moreover, no advantages over the latter process.
BY MEANS OF CHLORATE OF POTASSA.
The organic materials are treated with an equal weight of pure hydrochloric acid, and water added, so as to form a clear pulp. This being accomplished, two grammes of chlorate of potassa are added to the mixture at intervals of about five minutes. The fluid is next filtered, and the insoluble residue remaining on the filter washed until the wash-water ceases to exhibit an acid reaction. The filtrate is then evaporated, an aqueous solution of sulphurous acid added, until the odor of this reagent remains distinctly perceptible, and the excess of the acid removed by boiling the solution for about an hour. The fluid is now adapted to further examination for arsenic, or other metallic poisons.
This method is one of the best in use, both chlorate of potassa and hydrochloric acid being reagents easily procured in a state of great purity; their use, however, is liable to the objection that they convert silver and lead into insoluble chlorides.
BY MEANS OF CHLORINE.
M. Jacquelain suggests, in the search for arsenic, the decomposition of the organic matters by means of a current of chlorine, and recommends the following process: The organic substances are bruised in a mortar and then macerated with water. The fluid so obtained, in which the organic matter is held suspended, is next placed in a flask into which a current of chlorine is passed until all the organic matter is deposited in colorless flakes on the bottom of the vessel. The flask is then well closed and allowed to stand for 24 hours, when the odor of the gas should still be perceptible. The fluid is now filtered, the filtrate concentrated by heating in a vessel which permits of the preservation of the volatile chloride of arsenic possibly present, and then examined for poisons.
This process fails to possess the degree of generality desirable, and presents the disadvantage of requiring considerable time for its execution.