Interfacial sliding of polymer brushes: A molecular dynamics simulation

被引:128
作者
Grest, GS
机构
[1] Corporate Research Science Laboratories, Exxon Research and Engineering Company, Annandale, NJ
关键词
D O I
10.1103/PhysRevLett.76.4979
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Polymers end grafted to a surface have recently been shown to have an anomalously low effective friction coefficient mu(b). TO understand the origin of the observed reduction in friction, molecular dynamics simulations of polymers tethered at one end to a surface in a good solvent were carried out. As the surfaces are brought into contact, the normal force increases rapidly, while the shear force is found to be significantly smaller. For low shear velocity upsilon, the surfaces slide past each other with no change in the chain's radius of gyration or the amount of interpenetration. In this regime the shear force increases linearly with upsilon. For larger upsilon, there is significant chain stretching and disentanglement.
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页码:4979 / 4982
页数:4
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