Predicting thermal shape memory of crosslinked polymer networks from linear viscoelasticity

被引:184
作者
Diani, Julie [1 ]
Gilormini, Pierre [1 ]
Fredy, Carole [1 ]
Rousseau, Ingrid [2 ]
机构
[1] Arts & Metiers ParisTech, CNRS, PIMM, F-75013 Paris, France
[2] Gen Motors Co, Ctr Res & Dev, Warren, MI 48090 USA
关键词
Shape memory; Polymers; Modelling; Thermomechanical; Viscoelastic; Finite element; CONSTITUTIVE THEORY; POLYURETHANE; MODEL; RECOVERY;
D O I
10.1016/j.ijsolstr.2011.11.019
中图分类号
O3 [力学];
学科分类号
070301 [无机化学];
摘要
The viscoelastic behavior of an amorphous shape memory polymer network and its dependence on time and temperature were measured by dynamic mechanical analysis. The resulting thermo-mechanical behavior was modeled and implemented in a commercial finite element code. The ability of the resulting thermomechanical model to simulate and, eventually, predict the shape storage and shape recovery of the material was evaluated against experimental shape memory thermomechanical torsion data in a large deformation regimen. The simulations showed excellent agreement with experimental shape memory thermomechanical cycle data. This demonstrates the dependence of the shape recovery on time and temperature. The results suggest that accurate predictions of the shape recovery of any amorphous polymer networks under any thermomechanical conditions combination solely depends on considering the material viscoelasticity and its time-temperature dependence. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:793 / 799
页数:7
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