Effective interactions between oppositely charged polyelectrolytes in the presence of salt

被引:6
|
作者
Hansen, Jean-Pierre [2 ,3 ]
Coslovich, Daniele [1 ]
Kahl, Gerhard [4 ,5 ]
机构
[1] Univ Montpellier 2, CNRS, Lab Charles Coulomb, UMR 5221, Montpellier, France
[2] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
[3] Univ Paris 06, PECSA, Paris, France
[4] Vienna Univ Technol, Inst Theoret Phys, A-1060 Vienna, Austria
[5] Vienna Univ Technol, Ctr Computat Mat Sci, A-1060 Vienna, Austria
基金
奥地利科学基金会;
关键词
polyelectrolytes; colloids; Monte Carlo simulations; liquid structure; density functional theory; MODEL; SIMULATIONS; PARTICLES; BEHAVIOR; SYSTEMS;
D O I
10.1080/00268976.2011.621459
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
We generalize the familiar effective DLVO (Derjaguin-Landau-Verwey-Overbeek) pair potential between charged, hard core colloidal particles to the case of solutions of oppositely charged, penetrable polyelectrolyte coils in the presence of microions, within the framework of classical Density Functional Theory. The limiting behaviour of the effective potentials is derived in the limits of weak and strong microion screening; in the latter regime the effective potentials are shown to go over to a universal Gaussian form, multiplied by the square of the microion Debye screening length. The physical implications of screening on polyelectrolyte aggregation are discussed and illustrated by preliminary Monte Carlo simulations and the results of fluid integral equations for the polyelectrolyte pair structure.
引用
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页码:2953 / 2962
页数:10
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