Viscosities of electrolyte solutions

被引:30
作者
Waghorne, WE [1 ]
机构
[1] Univ Coll Dublin, Dept Chem, Dublin 4, Ireland
来源
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY OF LONDON SERIES A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES | 2001年 / 359卷 / 1785期
关键词
viscosity; B-coefficient; solvation; hydrophobic; aqueous solutions; non-aqueous solvents;
D O I
10.1098/rsta.2001.0864
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The effect of solute-solvent interactions on the viscosity of dilute electrolyte solutions is considered in terms of the solute contribution to the activation free energy, enthalpy or entropy, for viscous flow. Two classes of electrolyte are considered, those involving inorganic ions and those involving larger organic ions such as the tetraalkylammonium salts. The solute contributions to the activation free energies for viscous flow Delta mu (theta double dagger)(2) for inorganic electrolytes vary systematically with the charge and radius of the ion in a way that is consistent with a primarily electrostatic effect, increasing linearly with the ionic charge and with the inverse of the ionic radius. In contrast, the Delta mu (theta double dagger)(2) values for the tetraalkylammonium halides increase linearly with the cationic volume. For both types of electrolytes Delta mu (theta double dagger)(2) in organic solvents is relatively insensitive to the solvent, while the values for aqueous systems are markedly different from those in the organic solvents.
引用
收藏
页码:1529 / 1543
页数:15
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