Conductance of concentrated aqueous solutions of electrolytes. II. Strong polyvalent electrolytes

1970 ◽  
Vol 35 (8) ◽  
pp. 2244-2249 ◽  
Author(s):  
M. Postler
1906 ◽  
Vol 45 (1) ◽  
pp. 241-259 ◽  
Author(s):  
John Gibson

Although great advances have been made during the last thirty years in our knowledge of dilute solutions, there has been no corresponding advance in respect of concentrated solutions. This is primarily due to the fact that hitherto no simple and general relationship has been discovered between the conductivity and the concentration of concentrated solutions of electrolytes. Ostwald's law of dilution holds only for dilute solutions of weak electrolytes, and the formulæ of Rudolphi and Van T'Hoff are applicable only to dilute solutions of good electrolytes. It seems therefore important to inquire whether the difficulty may not be to some extent overcome by an alteration in the mode of representing the facts.


1908 ◽  
Vol 45 (4) ◽  
pp. 855-884 ◽  
Author(s):  
S. M. Johnston

In this paper the results of observations of the elevation of the boiling point of aqueous solutions of electrolytes are given, and a few results of observations of the depression of the freezing point, together with conductivity data obtained by observations of conductivity at about 99·4° and 0° Centigrade.


1906 ◽  
Vol 26 (1) ◽  
pp. 234-237
Author(s):  
J. Gibson

In a paper communicated to the Society in 1897, the author drew attention to increase in electrical conductivity as a characteristic of photo-chemical action, and in a second communication in December of the same year, made the following statement—“It would appear that the chemical behaviour of the acids just mentioned (HNO3, HCl, H2SO4) depends in many of their reactions on whether their concentration is above or below that corresponding to their maximum electrolytic conductivity.”


1977 ◽  
Vol 42 (9) ◽  
pp. 2642-2650
Author(s):  
F. Kaštánek ◽  
J. Kratochvíl ◽  
J. Pata ◽  
M. Rylek

1984 ◽  
Vol 49 (5) ◽  
pp. 1061-1078 ◽  
Author(s):  
Jiří Čeleda ◽  
Stanislav Škramovský

Based on the earlier paper introducing a concept of the apparent parachor of a solute in the solution, we have eliminated in the present work algebraically the effect which is introduced into this quantity by the additivity of the apparent molal volumes. The difference remaining from the apparent parachor after substracting the contribution corresponding to the apparent volume ( for which the present authors suggest the name metachor) was evaluated from the experimental values of the surface tension of aqueous solutions for a set of 1,1-, 1,2- and 2,1-valent electrolytes. This difference showed to be independent of concentration up to the very high values of the order of units mol dm-3 but it was directly proportional to the number of the free charges (with a proportionality factor 5 ± 1 cm3 mol-1 identical for all studied electrolytes). The metachor can be, for this reason, a suitable characteristic for detection of the association of ions and formation of complexes in the solutions of electrolytes, up to high concentrations where other methods are failing.


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