Interfacial tension and wetting in colloid-polymer mixtures

被引:45
作者
Aarts, DGAL
Dullens, RPA
Lekkerkerker, HNW
Bonn, D
van Roij, R
机构
[1] Univ Utrecht, Debye Inst, Vant Hoff Lab Phys & Colloid Chem, NL-3584 CH Utrecht, Netherlands
[2] Ecole Normale Super, Phys Stat Lab, F-75231 Paris 05, France
[3] Univ Amsterdam, Van der Waals Zeeman Inst, NL-1018 XE Amsterdam, Netherlands
[4] Univ Utrecht, Inst Theoret Phys, NL-3584 CE Utrecht, Netherlands
关键词
D O I
10.1063/1.1635810
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 calculate the interfacial tension and the wetting behavior in phase separated colloid-polymer mixtures both for ideal and excluded volume interacting polymers. Within the recently developed extension of the free volume theory to include polymer interactions [Aarts, Tuinier, and Lekkerkerker, J. Phys.: Condens. Matter 14, 7551 (2002)] the interfacial tension of the free interface is calculated by adding a van der Waals squared gradient term. The wetting behavior at a hard wall is calculated following a Cahn-Fisher-Nakanishi approach taking the one- and two-body colloid-wall interactions into account. Comparing results for interacting polymers with those for ideal polymers we find that for interacting polymers the interfacial tension does not increase as steeply as a function of the gas-liquid colloid density difference. Furthermore, the wetting transition shifts to higher polymer concentrations, even to above the triple line. The predictions for both the interfacial tension and the wetting are compared to recent experiments. (C) 2004 American Institute of Physics.
引用
收藏
页码:1973 / 1980
页数:8
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