Thermodynamic properties of multicomponent electrolyte solutions in mixed solvents. 5• HCl + NaCl + urea + water at 278.5–318.15 K

1988 ◽  
Vol 66 (4) ◽  
pp. 637-644 ◽  
Author(s):  
Dian-Yuan Men ◽  
Jia-Zhen Yang ◽  
Chun-Yu Liang ◽  
Li-Tian Zhang ◽  
Huan Gao ◽  
...  

This paper reports electromotive force measurements of the cells[Formula: see text]and[Formula: see text]in mixed solvents of urea, mole fraction x = 0.05, at five temperatures from 278.15 to 318.15 K. The standard potentials of Ag–AgCl electrode in mixed solvents were obtained from the emf of cell (A) for HCl of molality mA from 0.02 to 0.11 mol kg−1, both by extrapolation on the basis of an extended Debye–Hückel equation and by a polynomial approach proposed in this paper on the basis of Pitzer's electrolytic solution theory. The standard free energies of transfer for HCl are discussed. The activity coefficients of HClγA in HCl + NaCl + urea + water have also been obtained from the emf of cell (B) at constant total ionic strength I = 0.5, 1.0, 1.5, and 2.0 mol kg−1. The experimental results show that HCl obeys Harned's rule and log γA is a linear function of absolute temperature T. They also indicate that the relative partial molar enthalpy of HCl obeys a similar Harned's rule.


2005 ◽  
Vol 116 (2) ◽  
pp. 93-97 ◽  
Author(s):  
Farzad Deyhimi ◽  
Bahram Ghalami-Choobar ◽  
Rahman Salamat-Ahangari


1973 ◽  
Vol 51 (18) ◽  
pp. 3114-3122 ◽  
Author(s):  
Ron J. Robertson ◽  
Alfred S. Kucharski

Electromotive force measurements on the ZnCl2–ACl systems where A = K, Rb, and Cs were made using cells of the type[Formula: see text]in the temperature range 450° to 800 °C. The partial molar free energies, enthalpies, and excess entropies have been determined from the temperature dependence of the emf results. These thermodynamic properties exhibit increasing negative departure from ideality as the basicity of the alkali metal salt increases. The results are interpreted in terms of an acid–base reaction and are discussed in relation to current models.



2003 ◽  
Vol 217 (6) ◽  
pp. 637-652 ◽  
Author(s):  
Jianji Wang ◽  
Yang Zhao ◽  
Kelei Zhuo ◽  
Ruisen Lin

AbstractViscosities of LiClO4 and LiBr have been measured in solvent mixtures of propylene carbonate (PC) with dimethylformamide (DMF), tetrahydrofuran (THF), acetonitrile (AN) and methyl formate (MF) at 298.15K. The dependence of viscosity on the composition of the mixed solvents was fitted with an equation without adjustable parameter. Viscosity B-coefficients for lithium salts and the corresponding activation free energies (Δμ0,≠) for viscous flow have been evaluated. At the same time, viscosity B-coefficients were predicted by the dielectric friction theory. The unsuccessful prediction of the composition dependence of the B-coefficients indicates that improvements will be necessary on the theory with taking account of the short-range interaction and molecular nature of the solvents. Furthermore, solute–solvent interactions in these mixed solvents are discussed in terms of the B-coefficients and activation parameters.



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