Interactions of polyelectrolyte brushes with oppositely charged surfactants

被引:10
|
作者
Cao, Qianqian [1 ]
Zuo, Chuncheng [1 ]
Li, Lujuan [1 ]
Gao, Mingfeng [1 ]
机构
[1] Jilin Univ, Coll Mech Sci & Engn, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
Brownian dynamics; Polyelectrolyte brushes; Surfactants; Electrostatic binding; MOLECULAR-DYNAMICS SIMULATION; SODIUM DODECYL-SULFATE; CATIONIC SURFACTANTS; BROWNIAN DYNAMICS; BUILDING-BLOCKS; MICELLE; BINDING; COMPLEXES; POLYMERS; ASSOCIATION;
D O I
10.1007/s00396-011-2432-x
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
Using Brownian dynamics simulations, we study the effect of the charge ratio, the surfactant length, and the grafting density on the conformational behavior of the complex formed by the polyelectrolyte brush with oppositely charged surfactants. In our simulations, the polyelectrolyte chains and surfactants are represented by a coarse-grained bead-spring model, and the solvent is treated implicitly. It is found that varying the charge ratio induces different morphologies of surfactant aggregates adsorbed onto the brush. At high charge ratios, the density profiles of surfactant monomers indicate that surfactant aggregates exhibit a layer-by-layer arrangement. The surfactant length has a strong effect on the adsorption behavior of surfactants. The lengthening of surfactant leads to a collapsed brush configuration, but a reswelling of the brush with further increasing the surfactant length is observed. The collapse of the brush is attributed to the enhancement of surfactants binding to polyelectrolyte chains. The reswelling is due to an increase in the volume of adsorbed surfactant aggregates. At the largest grafting density investigated, enhanced excluded volume interactions limit the adsorption of surfactant within the polyelectrolyte brush. We also find that end monomers in polyelectrolyte chains exhibit a bimodal distribution in cases of large surfactant lengths and high charge ratios.
引用
收藏
页码:1089 / 1102
页数:14
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