The effect of solute concentration on fluidity and structure in aqueous solutions of electrolytes—I. Alkali-metal and ammonium halides

1964 ◽  
Vol 9 (2) ◽  
pp. 203-217 ◽  
Author(s):  
W. Good
1967 ◽  
Vol 45 (8) ◽  
pp. 2493-2503 ◽  
Author(s):  
P. A. Speight ◽  
R. L. Armstrong

The concentration dependence of the relaxation rates of 7Li and 23Na ion nuclei in aqueous solutions of alkali halides has been studied at 25 °C, using a pulsed magnetic resonance spectrometer operating at 3.75 MHz. The data are represented by empirical equations of the form:[Formula: see text]where T10−1 is the infinite dilution relaxation rate and C is the solute molarity. The infinite dilution rates are discussed with reference to the theoretical model considered by Hertz (1961). The concentration dependence is analyzed by using an extension of the method introduced by Eisenstadt and Friedman (1966) to include terms quadratic in the solute concentration.


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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