拉伸应力对聚对苯二甲酸乙二醇酯纤维结构形成过程中分子链延伸的影响

IF 4.1 2区 化学 Q2 POLYMER SCIENCE Polymer Pub Date : 2024-09-11 DOI:10.1016/j.polymer.2024.127605
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引用次数: 0

摘要

本研究调查了拉伸应力对纤维结构形成前聚对苯二甲酸乙二醇酯(PET)链延伸的影响,以及由此产生的纤维的机械和热机械性能。根据缩颈后观察到的胶相衍射分析了承受外力的分子链的数量、持续长度和延伸。对于分子量为 19,600 g/mol 的 PET 纤维,在低于临界值 99 MPa 的应力下拉伸时,观察到较小的 d 间距和较少的胶凝相数量、较慢的结晶速度和较长的结晶诱导时间。此外,临界应力值似乎随着分子量的增加而降低。当拉伸应力小于临界值时,缩颈后立即推算出的 d-间距会随着拉伸应力的降低而迅速减小,这种减小会导致拉伸纤维的抗拉强度和热收缩率降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Effects of drawing stress on the molecular-chain extension in fiber structure formation of poly(ethylene terephthalate)

In the present study, the effects of drawing stress on poly(ethylene terephthalate) (PET)-chain extension prior to fiber-structure formation as well as the mechanical and thermomechanical properties of the resulting fiber were investigated. The amount, persistence length, and extension of molecular chains bearing external force were analyzed from the diffraction of the smectic phase observed after necking. For PET fiber with a molecular weight of 19,600 g/mol drawn at a stress lower than the critical value of 99 MPa, less d-spacing and less amount of the smectic phase, slower crystallization, and longer crystallization-induction time were observed. Furthermore, the critical stress value appeared to decrease with increasing molecular weight. When the drawing stress was less than the critical value, the d-spacing extrapolated immediately after necking decreased rapidly with decreasing drawing stress, and this decrease leads to a decrease in the tensile strength and thermal shrinkage of the drawn fiber.

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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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