scholarly journals The electrolytic properties of diluted solutions of sulphuric acid

The first section of the present paper contains an account of a continuation of the work described in the 'Proceedings of the Royal Society,’ A, vol. 76, p. 577, 1905, and a statement of the object of the investigation may be reproduced from that place : “ If the measure of the electrical conductivity of a solution be divided by that of the concentration expressed in gramme-equivalents per unit volume, we obtain a quantity which may be called the equivalent conductivity of the solution. If the conductivity of the solvent used be subtracted from that of the solution, the corresponding quantity may be taken as giving the equivalent conductivity of the solute.

If the measure of the electrical conductivity of a solution be divided by that of the concentration expressed in gramme-equivalents per unit volume, we obtain a quantity which may be called the equivalent conductivity of the solution. If the conductivity of the solvent used be subtracted from that of the solution, the corresponding quantity may be taken as giving the equivalent conductivity of the solute. As is well known, the equivalent conductivity of neutral salts when dissolved in water approaches a limiting value as the dilution is increased, and, in terms of the ionisation theory, this limiting value corresponds with complete ionisation.


1857 ◽  
Vol 8 ◽  
pp. 158-165 ◽  

Since we had the honour of addressing the Royal Society upon the subject of the behaviour of acetamide and acetonitrile towards sulphuric acid, we have completed our experiments upon the amides and nitriles, and extended our researches to other groups of bodies. The results of these additional inquiries we now beg to present in the form of a second short summary, the analytical details and the more extended description of the new compounds being given in the complete memoir, which, at the same time, we have the honour of submitting to the Society.


1877 ◽  
Vol 25 (171-178) ◽  
pp. 322-327 ◽  

In presenting this communication to the Royal Society I wish to state that it is only an abstract of a more extensive paper on the same subject which I hope to publish shortly, and which contains an account of experiments with nearly seventy substances, most of which were never used before for such an investigation. I tried also nearly all the liquefied gases, and a considerable time was spent in preparing them for this kind of research, that was often interrupted by fearful explosions. The invaluable opportunity which Mr. Warren De La Rue, F. R. S., granted me some time ago to try the same compounds with his very powerful battery, led to results which I hope the Society will not consider devoid of interest.


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. 214-219 ◽  

The effects produced when concentrated hydro-sulphuric acid (oil of vitriol) is poured upon hyperoxymuriate of potassa, have been often objects of chemical discussion; the acid and the salt, it is well known, become deep orange, and if any moisture is present, or if heat is applied to the mixture, a detonation occurs. In a paper read before the Royal Society, I have ventured to suppose, that these phenomena depend upon the developement and sudden decomposition of the compound of chlorine and oxygene, which I have named euchlorine. A statement, which I understand has been made by M. Gay Lussac, namely, that a peculiar acid, which he has called chloric acid, may be procured from the hyperoxymuriate of baryta by sulphuric acid, led me to examine the action of acids on the hyperoxymuriates under new circumstances, and I have made some observations which appear to me not unworthy of being communicated to the Royal Society.


1968 ◽  
Vol 23 (6) ◽  
pp. 926-932
Author(s):  
Vittoriano Wagner ◽  
Sandro Forcheri

The electrical conductivity of molten (Na—Rb)NO3 and (Tl—Rb)NO3 was determined.While the equivalent conductivity of the first system shows the usual negative deviation from additivity, that of the second one varies nearly linearly with composition.After discussing the conductivity isotherms in terms of some proposed models, an excess conductivity isotherm is presented, derived on the basis of simple assumptions about the trend of both cationic mobilities.


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.


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