Chain entanglement in thin freestanding polymer films

被引:204
|
作者
Si, L [1 ]
Massa, MV
Dalnoki-Veress, K
Brown, HR
Jones, RAL
机构
[1] McMaster Univ, Dept Phys & Astron, Hamilton, ON L8S 4M1, Canada
[2] McMaster Univ, Brockhouse Inst Mat Res, Hamilton, ON L8S 4M1, Canada
[3] Univ Wollongong, Steel Inst, Wollongong, NSW 2500, Australia
[4] Univ Sheffield, Dept Phys & Astron, Sheffield, S Yorkshire, England
关键词
D O I
10.1103/PhysRevLett.94.127801
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
When a thin glassy film is strained uniaxially, a shear deformation zone (SDZ) can be observed. The ratio of the thickness of the SDZ to that of the undeformed film is related to the maximum extension ratio, lambda, which depends on the entanglement molecular weight, M-e. We have measured lambda as a function of film thickness in strained freestanding films of polystyrene as a probe of M-e in confinement. It is found that thin films stretch further than thick films before failure, consistent with the interpretation that polymers in thin films are less entangled than bulk polymers, thus the effective value of M-e in thin films is significantly larger than that of the bulk. Our results are well described by a conceptually simple model based on the probability of finding intermolecular entanglements near an interface.
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页数:4
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