To ascertain the composition of the compact nitrate of ammoniac, I exposed in a deep porcelain cup, 400 grains of the fibrous salt, in a temperature below 300°. It quickly became fluid, and slowly gave out its water without any ebullition, or liberation of gas. When it was become perfectly dry, it had lost 33 grains. I suspected, that in this experiment some of the salt had been carried off with the water; to determine this, I introduced into a small glass retort, 460 grains of fibrous salt; it was kept at a heat below 320°, in communication with a mercurial apparatus, in a regulated air-furnace, till it was perfectly dry: it had lost 23 grains. No gas, except the common air of the retort came over, and the fluid collected had but a faint taste of nitrate of ammoniac.
Though in this experiment I had removed all the fluid retained in the neck of the retort, still a few drops remained in the head, and on the sides, which I could not obtain. It was of importance to me to be accurately acquainted with the composition of the compact salt, and for that reason I compared these analytical experiments with a synthetical one.
I saturated 200 grains of solution of ammoniac, of,9056 with acid, ascertained the specific gravity of the solution, evaporated it at 212°, and fused and dried it at about 300°-260°. It gave 246 grains of salt, and a solution made of the same specific gravity as that evaporated, indicated a loss of 9 grains. Consequently, 255 grains of this salt contain 50,5 grains alkali, 100 grains acid, and 14,5 grains water.
We may then conclude, that 100 parts of compact nitrate of ammoniac contain 74,5 acid, 19,8 alkali, and 5,7 water.
V. Decomposition of Carbonate of Ammoniac by Nitric Acid.
In my first experiments on the production of nitrate of ammoniac, I endeavoured to ascertain its composition by decompounding carbonate of ammoniac by nitric acid; and in making for this purpose, the analysis of carbonate of ammoniac, I discovered that there existed many varieties of this salt, containing very different proportions of carbonic acid, alkali, and water; the carbonic acid and water being superabundant in it, in proportion as the temperature of its formation was low, and the alkali in proportion as it was high: and not only that a different salt was formed at every different temperature, but likewise that the difference in them was so great, that the carbonate of ammoniac formed at 300° contained more than 50 per cent alkali, whilst that produced at 60° contained only 20.[73]
I found 210 grains of carbonate of ammoniac, which from comparison with other salts previously analised, I suspected to contain about 20 or 21 per cent alkali, saturated by 200 grains of nitric acid of 1,504. But though the carbonate was dissolved in much water, still, from the smell of the carbonic acid generated, I suspect that a small portion of the nitric acid was dissolved, and carried off by it. The solution, evaporated at about 200°, and afterwards exposed to a temperature below 300°, gave 232 grains of compact salt. But reasoning from the quantity of acid in 200 grains of nitric acid of 1,504, it ought to have given 245. Consequently 13 were lost by evaporation; and this loss agrees with that in the other experiments.
VI. Decomposition of Sulphate of Ammoniac by Nitre.
As a cheap mode of obtaining nitrate of ammoniac, Dr. Beddoes proposed to decompose nitre by sulphate of ammoniac, which is a well known article of commerce. From synthesis of sulphate of ammoniac, compared with analysis made in August 1799,[74] I concluded that 100 grains of prismatic salt were composed of about 18 grains ammoniac, 44 acid, and 38 water; and supposing 100 grains of nitre to contain 50 acid, 100 grains of sulphate of ammoniac will require for their decomposition 134 grains of nitre, and form 90,9 grains of compact nitrate of ammoniac.
To ascertain if the sulphate of potash and nitrate of ammoniac could be easily separated, I added to a heated saturated solution of sulphate of ammoniac, pulverised nitre, till the decomposition was complete. After this decomposition, the solution contained a slight excess of sulphuric acid, which was combined with lime, and the whole set to evaporate at a temperature below 250°. As soon as the sulphate of potash began to crystalise, the solution was suffered to cool, and then poured off from the crystalised salt, which appeared to contain no nitrate of ammoniac. After a second evaporation and crystalisation, almost the whole of the sulphate appeared to be deposited, and the solution of nitrate of ammoniac was obtained nearly pure: it was evaporated at 212°, and gave fibrous crystals.