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首页> 外文期刊>Journal of Polymer Science, Part B. Polymer Physics >Dislocation approach to the plastic deformation of semicrystalline polymers: Kinetic aspects for polyethylene and polypropylene
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Dislocation approach to the plastic deformation of semicrystalline polymers: Kinetic aspects for polyethylene and polypropylene

机译:位错法处理半结晶聚合物的塑性变形:聚乙烯和聚丙烯的动力学方面

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The plasticity of semicrystalline polymers is analyzed in the framework of Young's dislocation model under the assumption of nucleation of screw dislocations from the lateral surface of the crystalline lamellae. It is proposed that the driving force for the nucleation and propagation across the crystal width of these screw dislocations relies on chain twist defects that migrate along the chains stems and allow a step-by-step translation of the stems through the crystal thickness. Such defects are identified as thermally activated conformational defects responsible for the so-called crystalline relaxation. Dislocation kinetic equations are derived. Plastic flow rates attainable by dislocation motion in polyethylene and polypropylene are assessed with frequency-temperature data of the crystalline relaxation. Comparisons are made with experimental strain rates that enable homogeneous plastic deformation. In addition to temperature, the crystal lamellar thickness, which is a basic factor of the plastic flow stress in Young's dislocation model, is a major factor in dislocation kinetics through its influence on chain twist activation. (C) 2002 Wiley Periodicals, Inc. [References: 64]
机译:在晶体位错从晶状薄层的侧面成核的假设下,在杨氏位错模型的框架内分析了半结晶聚合物的可塑性。提出了用于这些螺型位错的晶体宽度上的成核和传播的驱动力取决于沿着链茎迁移的链扭曲缺陷,并允许茎在晶体厚度上逐步移动。这些缺陷被鉴定为引起所谓的晶体弛豫的热活化构象缺陷。推导了位错动力学方程。在聚乙烯和聚丙烯中通过位错运动可获得的塑料流速是用晶体弛豫的频率-温度数据评估的。比较了能够​​实现均匀塑性变形的实验应变率。除了温度之外,晶体层厚度是杨氏位错模型中塑性流动应力的基本因素,也是影响位错动力学的主要因素,它对链扭曲活化有影响。 (C)2002 Wiley Periodicals,Inc. [参考:64]

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