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聚对苯二甲酸乙二酯双轴变形诱导相变的微观力学建模

Micromechanical Modeling of the Biaxial Deformation-Induced Phase Transformation in Polyethylene Terephthalate.

作者信息

Mamache Fateh Enouar, Mesbah Amar, Bian Hanbing, Zaïri Fahmi

机构信息

Laboratory of Advanced Mechanics, University of Sciences and Technology Houari Boumediene, Algiers 16111, Algeria.

Laboratoire de Génie Civil et géo-Environnement, Université de Lille, IMT Nord Europe, JUNIA, Université d'Artois, ULR 4515-LGCgE, F-59000 Lille, France.

出版信息

Polymers (Basel). 2022 Jul 26;14(15):3028. doi: 10.3390/polym14153028.

Abstract

In this paper, a micromechanics-based constitutive representation of the deformation-induced phase transformation in polyethylene terephthalate is proposed and verified under biaxial loading paths. The model, formulated within the Eshelby inclusion theory and the micromechanics framework, considers the material system as a two-phase medium, in which the active interactions between the continuous amorphous phase and the discrete newly formed crystalline domains are explicitly considered. The Duvaut-Lions viscoplastic approach is employed in order to introduce the rate-dependency of the yielding behavior. The model parameters are identified from uniaxial data in terms of stress-strain curves and crystallization kinetics at two different strain rates and two different temperatures above glass transition temperature. Then, it is shown that the model predictions are in good agreement with available experimental results under equal biaxial and constant width conditions. The role of the crystallization on the intrinsic properties is emphasized thanks to the model considering the different loading parameters in terms of mechanical path, strain rate and temperature.

摘要

本文提出了一种基于细观力学的聚对苯二甲酸乙二酯变形诱导相变的本构关系,并在双轴加载路径下进行了验证。该模型在埃舍尔贝夹杂理论和细观力学框架内建立,将材料系统视为两相介质,其中明确考虑了连续非晶相和离散新形成的结晶域之间的活性相互作用。采用杜瓦-利昂斯粘塑性方法来引入屈服行为的速率依赖性。根据在高于玻璃化转变温度的两种不同应变速率和两种不同温度下的应力-应变曲线和结晶动力学,从单轴数据中确定模型参数。然后表明,在等双轴和等宽度条件下,模型预测与现有实验结果吻合良好。由于该模型考虑了机械路径、应变速率和温度等不同加载参数,强调了结晶对本征性能的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/498a/9331422/ba6e5f5fa5d8/polymers-14-03028-g001.jpg

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