imperfections, arising principally from the presence and action of so much carbonaceous matter. The following was ultimately adopted.
A quantity of peroxide of copper was prepared by heating copper plates in air and scaling them. A sufficient quantity of pure muriatic and nitric acids were provided, and also a specimen of pure native carbonate of baryta. Seven grains of the salt to be examined were then mixed with seven grains of the pulverized carbonate of baryta, and afterwards with 312 grains of the oxide of copper. The mixture being put into a glass tube was successively heated throughout its mass, the gas liberated being passed through a mixture of baryta water and solution of muriate of baryta. It was found that no sulphurous or sulphuric acids came off; or indeed sulphur in any state. The contents of the tube were then dissolved in an excess of nitric and muriatic acids, above that required to take up all that was soluble; and a little solution of muriate of baryta was added for the sake of greater certainty. A portion of sulphate of baryta remained undissolved, equivalent to the sulphuric acid of the salt experimented upon, with that contained accidentally in the oxide of copper acids, &c. This sulphate was collected, washed, dried and weighed. Similar quantities of the carbonate of baryta and oxide of copper were then dissolved in as much of the nitric and muriatic acids as was used in the former experiment; and the washings and other operations being repeated exactly in the same way, the quantity of sulphate of baryta occasioned by the presence of sulphuric acid in the oxide, acids, &c. was determined. This, deducted from the weight afforded in the first experiments, gave the quantity produced from the sulphuric acid actually existing in the salt. Experiments so conducted gave very uniform results. The mean of many indicated 8.9 grains of sulphate of baryta for 10 grains of salt used, or 89 grains per cent., equivalent to 30.17 of sulphuric acid for every 100 of salt decomposed.
In the analytical experiments relative to the quantity of carbon and hydrogen contained in the salt, a given weight of the substance being mixed with peroxide of copper, was heated in a green glass tube. The apparatus used consisted of Mr. Cooper's lamp furnace, with Dr. Prout's mercurial trough; and all the precautions that could be taken, and which are now
