Nonelectrostatic Adsorption of Polyelectrolytes and Mediated Interactions between Solid Surfaces

被引:13
作者
Balzer, Christopher [1 ]
Jiang, Jian [2 ,3 ]
Marson, Ryan L. [4 ]
Ginzburg, Valeriy V. [4 ]
Wang, Zhen-Gang [1 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
[2] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, State Key Lab Polymer Phys & Chem, Beijing 100190, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Dow Chem Co USA, Res & Dev, Midland, MI 48674 USA
关键词
DENSITY-FUNCTIONAL THEORY; DIRECTIONAL ATTRACTIVE FORCES; FUNDAMENTAL-MEASURE-THEORY; HARD-SPHERE MIXTURES; CHARGED SURFACES; WEAK POLYELECTROLYTES; COLLOIDAL PARTICLES; INTEGRAL-EQUATION; BLOCK-COPOLYMERS; LATEX-PARTICLES;
D O I
10.1021/acs.langmuir.1c00139
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polymer-mediated interaction between two solid surfaces is directly connected to the properties of the adsorbed polymer layers. Nonelectrostatic interactions with a surface can significantly impact the adsorption of polyelectrolytes to charged surfaces. We use a classical density functional theory to study the effect of various polyelectrolyte solution properties on the adsorption and interaction between two like-charged surfaces. Our results show that nonelectrostatic interactions not only enhance polyelectrolyte adsorption but can also result in qualitatively different salt effects with respect to the adsorbed amount. In particular, we observe decreasing, increasing, and a previously unreported nonmonotonic behavior in the adsorbed amount of polymer with added salt under the conditions studied, although the nonmonotonic regime only occurs for a narrow range in the parameter space. With sufficient nonelectrostatic adsorption, the adsorbed polymer layers produce a long-range repulsive barrier that is strong enough to overcome dispersive interactions that cause surfaces to attract. Concurrently, a short-range bridging attraction is observed when the two polyelectrolyte layers span both the surfaces. Both the repulsive barrier and bridging attraction depend on the charge density of the polymer backbone and the bulk salt concentration but not on the chain length in the semidilute regime studied.
引用
收藏
页码:5483 / 5493
页数:11
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