A theoretical study of colloidal forces near amphiphilic polymer brushes

被引:7
|
作者
Lima, Eduardo R. A. [1 ,2 ,3 ]
Jiang, Tao [1 ,4 ]
Wu, Jianzhong [1 ]
机构
[1] Univ Calif Riverside, Dept Chem & Environm Engn, Riverside, CA 92521 USA
[2] Univ Fed Rio de Janeiro, Programa Engn Quim, BR-21941914 Rio de Janeiro, Brazil
[3] Univ Estado Rio De Janeiro, Inst Quim, BR-20550900 Rio De Janeiro, Brazil
[4] Calif Energy Commiss, Sacramento, CA 95814 USA
基金
美国国家科学基金会;
关键词
Density functional theory; Surface forces; Polymer brush; SELF-ASSEMBLED MONOLAYERS; PROTEIN ADSORPTION; BLOCK-COPOLYMERS; SURFACES; PARTICLES; EFFICIENT; MIXTURES; DENSITY;
D O I
10.1016/j.colsurfa.2011.03.031
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
Polymer-based "non-stick" coatings are promising as the next generation of effective, environmentally friendly marine antifouling systems that minimize non-specific adsorption of extracellular polymeric substances (EPS). However, design and development of such systems are impeded by the poor knowledge of polymer-mediated interactions of biomacromolecules with the protected substrate. In this work, a polymer density functional theory (OFT) is used to predict the potential of mean force between spherical biomacromolecules and amphiphilic copolymer brushes within a coarse-grained model that captures essential non-specific interactions such as the molecular excluded volume effects and the hydrophobic energies. The relevance of theoretical results for practical control of the EPS adsorption is discussed in terms of the efficiency of different brush configurations to prevent biofouling. It is shown that the most effective antifouling surface may be accomplished by a good balance of the polymer chain length and the grafting density. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:115 / 120
页数:6
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