Frictional Forces between Strongly Compressed, Nonentangled Polymer Brushes: Molecular Dynamics Simulations and Scaling Theory

被引:108
|
作者
Galuschko, A. [1 ]
Spirin, L. [2 ]
Kreer, T. [1 ]
Johner, A. [1 ]
Pastorino, C. [3 ]
Wittmer, J. [1 ]
Baschnagel, J. [1 ]
机构
[1] Inst Charles Sadron, F-67034 Strasbourg 2, France
[2] Johannes Gutenberg Univ Mainz, Inst Phys, D-55099 Mainz, Germany
[3] CNEA, CAC, Dept Phys, RA-1650 Buenos Aires, DF, Argentina
关键词
GOOD SOLVENT CONDITIONS; SHEAR FORCES; LUBRICATION; MECHANISMS; ADHESION; RHEOLOGY; STEADY; LAYERS;
D O I
10.1021/la904119c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
By means of molecular dynamics simulations and scaling theory we study the response or opposing polymer brushes to constant shear motion under good solvent conditions. Model systems that contain explicit solvent molecules (Lennard-Jones dimers) are compared to solvent-free systems while varying of the distance between the grafted layers and their molecular parameters, chain length and grafting density. Our study reveals a power-law dependence of macroscopic transport properties on the Weissenberg number, W, beyond linear response. For instance, we find that the kinetic friction constant scales as mu similar to W-0.57 for large values of W. We develop a scaling theory that describes our data and previous numerical data including recent experiments.
引用
收藏
页码:6418 / 6429
页数:12
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