The solvation shell in ionic solutions:: variational mean spherical scaling approximation
被引:3
作者:
Blum, L
论文数: 0引用数: 0
h-index: 0
机构:Univ Puerto Rico, Dept Phys, Rio Piedras, PR 00931 USA
Blum, L
Velázquez, ES
论文数: 0引用数: 0
h-index: 0
机构:Univ Puerto Rico, Dept Phys, Rio Piedras, PR 00931 USA
Velázquez, ES
机构:
[1] Univ Puerto Rico, Dept Phys, Rio Piedras, PR 00931 USA
[2] Univ Calif Santa Barbara, Inst Theoret Phys, Santa Barbara, CA 93106 USA
[3] Univ Puerto Rico, Dept Phys, Mayaguez, PR 00681 USA
来源:
JOURNAL OF MOLECULAR STRUCTURE-THEOCHEM
|
1999年
/
493卷
关键词:
ionic solvation;
solvation shells;
variational mean spherical approximation;
scaling theory;
D O I:
10.1016/S0166-1280(99)00245-6
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
The non-specific solvent effects in neutral dipolar (or better yet, effective dipolar) solvents were discussed in the literature with success, However the situation is not so clear when the solvent is an electrolyte, where the reaction field approach is no longer valid. In the present communication we present a theory based on the Mean Spherical Scaling Approximation in which the system is encapsulated in a ionic cloud that is represented by an equivalent capacitor of shape determined by precise prescriptions derived from exact relations and sum rules. The construction of the equivalent capacitor depends on the geometry of the system, on the nature of the solvent and on the nature and concentration of the ions. The treatment proposed here satisfies exact relations like the Stillinger-Lovett sum rules, the perfect screening sum rules, and the high and low coupling conditions and constitutes an interpolation scheme between exact high density and low density limits in it simplest form. The calculation is illustrated with an example of an ellipsoidal cavity. (C) 1999 Elsevier Science B.V. All rights reserved.