Predicting the stress relaxation behavior of glass-fiber reinforced polypropylene composites

被引:33
|
作者
Obaid, Numaira [1 ]
Kortschot, Mark T. [1 ]
Sain, Mohini [2 ]
机构
[1] Univ Toronto, Dept Chem Engn & Appl Chem, 200 Coll St, Toronto, ON M5S 3E5, Canada
[2] Univ Toronto, Ctr Biocomposites & Biomat Proc, Fac Forestry, 33 Willcocks St, Toronto, ON M5S 3B3, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Polymer-matrix composites (PMCs); Short-fiber composites; Stress relaxation; Modelling; Stress transfer; TIME EVOLUTION; MATRIX; ORIENTATION; STRENGTH; FRACTURE; CREEP;
D O I
10.1016/j.compscitech.2018.04.004
中图分类号
TB33 [复合材料];
学科分类号
摘要
It is well established that the addition of short elastic fibers slows the relaxation process in composites, but this phenomenon is not well-understood. Our recent study explained changes in the stress relaxation constant by accounting for the time-dependent interfacial shear stress transfer at the fiber-matrix interface. An analytical model was developed and was successfully compared to finite-element experiments. This approach represents a significant departure from the previously published literature, where the effect of fibers on viscoelasticity was typically attributed to changes in the covalent bonds at the fiber-matrix interface. In the present study, the stress relaxation behavior of glass fiber-reinforced polypropylene composites was experimentally measured and compared to analytical model predictions. Further, the effect of additional covalent bonding at the fiber-matrix interface was studied experimentally by introducing an interfacial coupling agent. Good agreement was obtained between the experimental data and the analytical model and it was concluded that most of the stress relaxation behavior of a composite can be predicted using a model that only accounts for the time-dependent matrix modulus and a time-dependent shear stress transfer efficiency.
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页码:85 / 91
页数:7
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