On the mutual action of sulphuric acid and alcohol, with observations on the composition and properties of the resulting compound

At the commencement of this paper Mr. Hennell describes certain peculiarities in the properties of oil of wine, which induced him to consider sulphuric acid as one of its proximate elements; and on following up his analytical experiments upon it he found that about 37 per cent, of that acid might be obtained during its decomposition, although in its original state it affords no indications of that acid by the tests of the soluble salts of baryta,—a circumstance which he refers to the presence of hydrocarbon exerting a peculiar saturating influence upon the acid. Of this hydrocarbon he next determines the composition, and finds that its elements correspond in their relative proportions with those of olefiant gas. When oil of wine is mixed with solution of muriate of baryta, and gently heated, the mixture becomes acid, reddening litmus paper, but yet does not precipitate the barytic salt. Several experiments are detailed illustrating the nature of this acid, from which it appears that it forms very soluble compounds with baryta and potassa; the latter is a crystallizable salt, which burns with flame when heated, and leaves a bisulphate of potassa. Its analysis, the details of which are given at length in the paper, shows it to consist of two proportionals of sulphuric acid, one of potassa, four of carbon, and four of hydrogen; and it is remarked that the latter elements, namely, the carbon and hydrogen, appear in the present instance to be equivalent to, or to exert a saturating power over, one of the proportionals of sulphuric acid. Some slight discrepancies between the experimental and theoretical results of these analyses are adverted to, which the author thinks himself justified in attributing to water of crystallization in the salt, which he could not succeed in obtaining in a perfectly anhydrous state.

2016 ◽  
Vol 869 ◽  
pp. 155-158
Author(s):  
Camila Machado de Oliveira ◽  
Adilson Oliveira ◽  
Jeane Almeida do Rosário ◽  
Agenor de Noni Jr. ◽  
Michael Peterson

Pyrite, mineral largely found in nature, is considered a solid waste when is obtained from the coal mining. However, can be precursor of products like: sulphur, sulphuric acid, hematite, sulphur dioxide, fertilizers and iron sulfates. Several studies also point it property of semiconduction and it use in solar cells. Increase it purity level is important for transforming it in products with more aggregate value. Thus, the present work suggests a purification route for the reduction in soluble salts in water, organics and quartz associated with pyrite from the coal mining beneficiation. The used methods were solubilization in hot water and in organic solvent (dichloromethane). Were applied XRD, FTIR, total sulphur determination, and gas helium picnometry. Comparing the results obtained for the “in nature” pyrite with the purified one, proved the efficiency of the proposed method.


1826 ◽  
Vol 116 ◽  
pp. 140-162 ◽  

In a Paper on new compounds of carbon and hydrogen , lately honoured by the Royal Society with a place in the Philosophical Transactions, I had occasion briefly to notice, the peculiar action exerted on certain of those compounds by sulphuric acid. During my attempts to ascertain more minutely the general nature of this action, I was led to suspect the occasional combination of the hydro-carbonaceous matter with the acid, and even its entrance into the constitution of the salts, which the acid afterwards formed with bases. Although this opinion proved incorrect, relative to the peculiar hydro-carbons forming the subject of that Paper, yet it led to experiments upon analogous bodies, and amongst others, upon naphthaline, which terminated in the production of the new acid body and salts now to be described. Some of the results obtained by the use of the oil gas products are very peculiar. If, when completed, I find them sufficiently interesting, I shall think it my duty to place them before the Royal Society, as explicatory of that action of sulphuric acid which was briefly noticed in my last Paper.


1815 ◽  
Vol 105 ◽  
pp. 203-213 ◽  

In the two papers containing researches on iodine which the Royal Society has done me the honour of publishing in the Transactions, I have described a class of bodies consisting of iodine, oxygene, and different bases analogous to the hyper-oxymuriates. In the last of these papers, I mentioned, that I had not been able to procure any binary combination of iodine and oxygene from these compounds, neither by the method proposed by M. Gay Lussac, namely, the action of sulphuric acid on the oxyiode of barium, nor by other methods of my own institution; and that in experiments on the effects of the acids on the oxyiodes, new combinations only were formed. I have lately resumed this enquiry, and by pursuing a new and entirely different plan of operation, I have at last succeeded in combining oxygene and iodine. In the following pages I shall describe the circumstances which led me to ascertain the existence of this compound, and I shall detail some experiments on its analysis and its chemical agencies. In the course of my researches, I observed, that when a solution of the compound of iodine and chlorine was poured into alkaline solutions, or even into certain muriatic solutions, the precipitate was an oxyiode; and this fact seemed to indicate, that iodine had a stronger attraction for oxygene than chlorine; iodine, likewise, has an attraction for chlorine; it appeared, therefore, extremely probable, that euchlorine, or the gaseous combination of oxygene and chlorine, would be decomposed by heat, and two compounds formed, one of oxygene and iodine, and the other of iodine and chlorine, or that a triple compound would be produced from which chlorine could be easily separated, and on submitting the idea to the test of experiment, I found that I had not been deceived.


1857 ◽  
Vol 3 ◽  
pp. 482-486
Author(s):  
Balfour Stewart
Keyword(s):  

The object of this paper was to show that where sulphuric acid combines with water, distinct reference is made to certain definite compounds or hydrates of sulphuric acid.


In this communication Mr. Faraday shows that when sulphuric acid and naphthaline act upon each other, a peculiar compound pos­sessed of distinct acid characters is the result. This acid is most readily obtained by heating two parts of naphthaline with one of sulphuric acid. The mixture concretes on cooling, and separates into two parts, the uppermost of which is little else than naphthaline, but the lower, heavier part contains the peculiar acid, which, being soluble in water, is easily separated by that fluid, not, however, pure, but still containing mixed sulphuric acid. The author, however, ob­tained the pure acid by decomposing its compound with baryta, which is soluble, by sulphuric acid. It then had a bitter sour taste, and formed a distinct class of salts with the different bases, all of which are soluble in water and in alcohol, and combustible. By careful evaporation of the aqueous solution of this acid, a white crystalline deliquescent solution was obtained, evolving water when heated, and at high temperatures affording sulphurous acid, char­coal, and naphthaline. To determine the ultimate component parts of this acid, its compound with baryta was subjected to rigid analysis.


1899 ◽  
Vol 22 ◽  
pp. 484-522
Author(s):  
Sydney A. Kay

In the year 1847, as one of the results of an investigation to determine the part played by the mass action of water in chemical reactions, H. Rose (Pogg. Ann., lxxxii. 545) showed that an acid sulphate in aqueous solution is progressively decomposed into free acid and neutral sulphate by increasing quantities of water. His observations were confirmed and extended by the thermo-chemical researches of Thomsen (Pogg. Ann. 1869, cxxxviii. 72), and Berthelot (Ann. Chim. Phys., 1873, xxix. 433), who indicated more exactly the course and extent of this decomposition, and from whose work it is known that in the solution of an acid sulphate there exist free sulphuric acid, neutral sulphate and acid sulphate. Finally Ostwald, in his first memoir on chemical affinity (Jour, prakt. Cliem. 1879, xix. 483), showed how to determine the magnitude of this decomposition, and was able to approximately measure the quantity of free acid in solutions of the acid sulphates at different dilutions. In a later paper (ibid., 1880, xxii. 305), Ostwald investigated the question of the influence of water on the action between sulphuric acid and a neutral sulphate. He measured the changes of volume which occurred when solutions of sulphuric acid and sodium sulphate were mixed in varying proportions, and at different dilutions, and obtained results in agreement with his previous work. He also pointed out, that if the mutual action between the acid and neutral sulphate obeyed the general law of mass action, it should follow that, for example, one molecule sodium sulphate plus three molecules sulphuric acid, give the same quantity of acid sulphate as one molecule sulphuric acid, and three molecules sodium sulphate, the volume of the mixture being the same in each case.


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