确定单轴拉伸后微观结构方案的聚(2,5-呋喃二甲酸乙烯酯)极值图:取向与结晶之间的联系

IF 4.1 2区 化学 Q2 POLYMER SCIENCE
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引用次数: 0

摘要

通过基于极值和取向因子计算的创新方法,对新兴生物基聚合物聚(乙烯-2,5-呋喃二甲酸酯)PEF 进行了研究。在不同的机械条件(不同的等效应变率)下对 PEF 进行了单轴拉伸,拉伸应变可达到多个级别,同时还考虑了不同的拉伸后冷却条件(中断、无负荷和破裂样品)。在自然拉伸比(NDR)(材料开始应变硬化的变形)之前和之后对样品进行拉伸和中断。当 PEF 发生应变硬化时,它的结晶取向和结晶度比都会随着施加的变形而增加。在温度下卸载材料会降低部分结晶取向,尤其是链的脂肪族部分。此外,将 PEF 拉伸至高于 NDR 的高应变会导致晶体破碎。所有实验结果都与纹理模型进行了比较。由于呋喃循环趋向于平行于试样平面,因此拉伸后可形成接近纤维纹理的纹理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Poly(ethylene 2,5-furandicarboxylate) pole figures to determine the microstructural scheme upon uniaxial stretching: Link between orientation and crystallisation

Poly(ethylene 2,5-furandicarboxylate) pole figures to determine the microstructural scheme upon uniaxial stretching: Link between orientation and crystallisation

The emergent biobased polymer poly (ethylene 2,5-furandicarboxylate), PEF, has been studied through an innovative approach based on pole figures and orientation factor calculation. PEF uniaxial stretching was performed with different mechanical conditions (different equivalent strain rates), up to several levels of strain and while considering different post-stretching cooling conditions (interrupted, unloaded and ruptured samples). Samples were stretched and interrupted before and after the Natural Draw Ratio (NDR), the deformation for which the material starts strain-hardening. When PEF strain-hardens, it reveals both an increase of the crystalline orientation and crystallinity ratio with the deformation imposed. Unloading the material at temperature tends to decrease partially crystalline orientation, especially regarding the aliphatic part of the chains. Moreover, stretching PEF up to high strains, superior to the NDR, leads to crystal fragmentation. After all, all experimental results were compared to a texture model. It appears that a texture can be developed upon stretching that is close to a fibre texture, as the furan cycles tend to be parallel to the specimen plane.

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来源期刊
Polymer
Polymer 化学-高分子科学
CiteScore
7.90
自引率
8.70%
发文量
959
审稿时长
32 days
期刊介绍: Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics. The main scope is covered but not limited to the following core areas: Polymer Materials Nanocomposites and hybrid nanomaterials Polymer blends, films, fibres, networks and porous materials Physical Characterization Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films Polymer Engineering Advanced multiscale processing methods Polymer Synthesis, Modification and Self-assembly Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization Technological Applications Polymers for energy generation and storage Polymer membranes for separation technology Polymers for opto- and microelectronics.
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