Extension of an improved one-fluid conformal solution theory to real fluid mixtures with large size differences

1990 ◽  
Vol 11 (1) ◽  
pp. 87-96 ◽  
Author(s):  
M. L. Huber ◽  
J. F. Ely

1987 ◽  
Vol 37 ◽  
pp. 105-121 ◽  
Author(s):  
Marcia L. Huber ◽  
James F. Ely


1975 ◽  
Vol 30 (1) ◽  
pp. 64-68 ◽  
Author(s):  
H. C. Brookes ◽  
R. L. Paul

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.





2021 ◽  
Author(s):  
Simon Stephan ◽  
Hans Hasse

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.



2006 ◽  
Vol 241 (1-2) ◽  
pp. 147-154 ◽  
Author(s):  
M. Scott Shell ◽  
Pablo G. Debenedetti ◽  
Athanassios Z. Panagiotopoulos


1968 ◽  
Vol 49 (6) ◽  
pp. 2882-2882
Author(s):  
H. Ted Davis ◽  
John McDonald


1984 ◽  
Vol 51 (5) ◽  
pp. 1181-1192 ◽  
Author(s):  
James I.C. Chang


AIChE Journal ◽  
1971 ◽  
Vol 17 (1) ◽  
pp. 167-170
Author(s):  
Richard A. Gaggioli ◽  
Dale E. Nierode


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