Stress relaxation in polymer networks: Equilibrium behavior and dynamics

被引:4
作者
Adams, J. M.
Mao, Y.
Vandoolaeghe, W. L.
机构
[1] Univ Cambridge, Cavendish Lab, Cambridge CB3 0HE, England
[2] Univ Nottingham, Sch Phys & Astron, Nottingham NG7 2RD, England
关键词
D O I
10.1063/1.2768921
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
The elastic and relaxational properties of a polymer network have been calculated using a stress based formulation based on the Rouse mode expansion [W. L. Vandoolaeghe and E. M. Terentjev, J. Chem. Phys. 123, 34902 (2005)]. In this article, we propose an improved Rouse mode expansion incorporating appropriate boundary conditions. In contrast to the previous work, this improved formulation provides a smooth crossover from the classical equilibrium result of rubber elasticity to the shorter-time-scale Rouse relaxation of a polymer melt. Our results are compared with the classical phantom network approach in equilibrium, as well as both equilibrium and dynamic elongation experiments. The model captures the qualitative features of the data well and some of the quantitative aspects, such as the exponents seen in the dynamic modulus G(omega). (c) 2007 American Institute of Physics.
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页数:5
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