Erratum: Conformal Solution Theory of Certain Molten Salts

1968 ◽  
Vol 49 (6) ◽  
pp. 2882-2882
Author(s):  
H. Ted Davis ◽  
John McDonald
Keyword(s):  
Molten Salts ◽  
Solution Theory ◽  
Conformal Solution Theory

Conformal Solution Theory of Certain Molten Salts

1968 ◽  
Vol 48 (4) ◽  
pp. 1644-1650 ◽  
Author(s):  
H. Ted Davis ◽  
John McDonald
Keyword(s):  
Molten Salts ◽  
Solution Theory ◽  
Conformal Solution Theory

Densities and Excess Volumes of Fused Halides

1975 ◽  
Vol 30 (1) ◽  
pp. 64-68 ◽  
Author(s):  
H. C. Brookes ◽  
R. L. Paul
Keyword(s):  
Mole Fraction ◽  
Linear Dependence ◽  
Alkali Halide ◽  
Experimental Error ◽  
Van Der Waals ◽  
Excess Volumes ◽  
Van Der Waals Interactions ◽  
Solution Theory ◽  
Conformal Solution Theory ◽  
Volumes Of Mixing

Abstract Densities of molten AgBr-AX (A = Li, Na, K, Rb, Cs; X = Br or Cl), AgBr-AgCl, KBr-NaBr, KBr-CsBr, KCl-KBr, and KCl-CsBr mixtures have been measured at 0.5 mole fraction using the method of Archimedean displacement. The excess volumes of mixing are all positive, except for the AgBr-LiBr system. Attempts to relate the excess volumes of the binary AgBr-ABr systems to the second order conformal solution theory of Reiss, Katz, and Kleppa are unsuccessful, since V E is large even when the diameter difference parameter, δ12, is close to zero. However, the excess volumes of the reciprocal AgBr-ACl systems at 0.5 mole fraction are found, within experimental error, to have a linear dependence on δ12. The positive deviations from conformal solution theory which occur for the alkali halide mixtures have been interpreted in terms of non-Coulombic polarisation and van der Waals interactions.

scholarly journals Molecular Interactions at Vapor-Liquid Interfaces Binary Mixtures of Simple Fluids

2021 ◽  
Author(s):  
Simon Stephan ◽  
Hans Hasse
Keyword(s):  
Liquid Phase ◽  
Interfacial Properties ◽  
Binary Interaction ◽  
Binary Interaction Parameter ◽  
Gradient Theory ◽  
Solution Theory ◽  
Conformal Solution Theory ◽  
Vapor Liquid Equilibria ◽  
Dynamics Simulations ◽  
Vapor Liquid

Properties of vapor-liquid equilibria and planar interfaces of binary Lennard-Jones truncated and shifted mixtures were investigated with molecular dynamics simulations, density gradient theory, and conformal solution theory at constant liquid phase composition and temperature. The results elucidate the influence of the liquid phase interactions on the interfacial properties (surface tension, surface excess, interfacial thickness, and enrichment). The studied mixtures differ in the ratios of the dispersion energies of the two components ɛ2/ɛ1 and the binary interaction parameter ξ. By varying ξ and ɛ2/ɛ1, a variety of types of phase behavior is covered by this paper. The dependence of the interfacial properties on the variables ξ and ɛ2/ɛ1 reveals regularities that can be explained by conformal solution theory of the liquid phase. It is thereby shown that the interfacial properties of the mixtures are dominated by the mean liquid phase interactions whereas the vapor phase has only a minor influence.

A conformal solution theory for the energy landscape and glass transition of mixtures

2006 ◽  
Vol 241 (1-2) ◽  
pp. 147-154 ◽  
Author(s):  
M. Scott Shell ◽  
Pablo G. Debenedetti ◽  
Athanassios Z. Panagiotopoulos
Keyword(s):  
Glass Transition ◽  
Energy Landscape ◽  
Solution Theory ◽  
Conformal Solution Theory
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