Vorselaars Bart, Lyulin Alexey V, Michels M A J
Group Polymer Physics and Eindhoven Polymer Laboratories, Technische Universiteit Eindhoven, P. O. Box 513, 5600 MB Eindhoven, The Netherlands.
J Chem Phys. 2009 Feb 21;130(7):074905. doi: 10.1063/1.3077859.
The toughness of a polymer glass is determined by the interplay of yielding, strain softening, and strain hardening. Molecular-dynamics simulations of a typical polymer glass, atactic polystyrene, under the influence of active deformation have been carried out to enlighten these processes. It is observed that the dominant interaction for the yield peak is of interchain nature and for the strain hardening of intrachain nature. A connection is made with the microscopic cage-to-cage motion. It is found that the deformation does not lead to complete erasure of the thermal history but that differences persist at large length scales. Also we find that the strain-hardening modulus increases with increasing external pressure. This new observation cannot be explained by current theories such as the one based on the entanglement picture and the inclusion of this effect will lead to an improvement in constitutive modeling.
聚合物玻璃的韧性取决于屈服、应变软化和应变硬化之间的相互作用。为了阐明这些过程,对典型的聚合物玻璃——无规聚苯乙烯在主动变形影响下进行了分子动力学模拟。观察到屈服峰的主要相互作用是链间性质的,而应变硬化是链内性质的。与微观的笼间运动建立了联系。发现变形不会导致热历史的完全消除,而是在大长度尺度上差异仍然存在。我们还发现,应变硬化模量随外部压力的增加而增加。这一新观察结果无法用当前的理论来解释,比如基于缠结图像的理论,而纳入这一效应将有助于改进本构模型。