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A constitutive model for strain hardening behavior of predeformed amorphous polymers: Incorporating dissipative dynamics of molecular orientation

机译:预变形非晶聚合物应变硬化行为的本构模型:结合分子取向的耗散动力学

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A series of uniaxial compression tests are performed on amorphous thermoplastics poly (ethylene terephthalate)-glycol (PETG). The stress response shows a dramatic change with temperature and strain rate, including the modulus, yield strength and strain hardening. The strain hardening behavior also shows a strong dependence on predeformation, representing as a less pronounced hardening response during the reloading process with increasing the predeformation temperature and decreasing the predeformation rate. This phenomenon cannot be described by the models assuming a temperature-dependent hardening modulus. In this work, we develop a thermodynamic consistent model, which employs a dissipative back-stress tensor for molecular orientation. With increasing temperature, a stronger relaxation occurs, resulting in less molecular orientation and hardening response. A numerical scheme is also constructed to determine the model parameters. Comparison with experiments shows that the model is able to reproduce all the main features of the stress response at various strain rates spanning the glass transition region. The model can also accurately capture the strain hardening response of polymers predeformed to a strain of 30% or 60% at various temperatures and rates. (C) 2019 Elsevier Ltd. All rights reserved.
机译:对无定形热塑性聚对苯二甲酸乙二醇酯(PETG)进行了一系列单轴压缩测试。应力响应显示出随温度和应变速率的急剧变化,包括模量,屈服强度和应变硬化。应变硬化行为也显示出对预变形的强烈依赖性,表现为在重新加载过程中,随着预变形温度的升高和预变形速率的降低,淬火响应变得不那么明显。假设温度依赖的硬化模量的模型无法描述这种现象。在这项工作中,我们开发了一个热力学一致模型,该模型采用耗散背应力张量进行分子定向。随着温度升高,发生更强的弛豫,导致分子取向和硬化反应变少。还构造了一种数值方案来确定模型参数。与实验的比较表明,该模型能够重现跨越玻璃化转变区域的各种应变速率下应力响应的所有主要特征。该模型还可以准确地捕获在各种温度和速率下预变形为30%或60%应变的聚合物的应变硬化响应。 (C)2019 Elsevier Ltd.保留所有权利。

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