利用高分子量 PBT 制备高强度纤维的可行性和合理性

IF 4.1 2区 化学 Q2 POLYMER SCIENCE Polymer Pub Date : 2024-08-11 DOI:10.1016/j.polymer.2024.127484
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引用次数: 0

摘要

聚对苯二甲酸乙二醇酯(PET)工业丝由于柔韧性不足,在织造过程中容易损坏。因此,能否利用柔韧性更好的聚对苯二甲酸丁二醇酯(PBT)来生产高强度、低模量的工业丝值得探讨。本研究采用了低速纺丝多级多比率牵伸技术路线进行纺丝,但 PBT 纤维的断裂强度仅为 5.1cN/dtex,低于 PET 纤维(7.2cN/dtex)。通过比较 PET 和 PBT 在纺丝过程中的多层次结构演变,发现限制 PBT 纤维强度提高的核心问题是 PBT 纺丝纤维在冷却过程中早期形成的折叠链片层结构,这阻碍了热拉伸过程中的构象转变,限制了拉伸率。这对于通过调整 PBT 无纺纤维的结晶特性来发展 PBT 工业丝技术具有重要意义。
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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The feasibility and rationale for utilizing high molecular weight PBT in the preparation of high-strength fiber

Polyethylene terephthalate (PET) industrial yarn is prone to damage during weaving due to its insufficient flexibility. Therefore, it is worth exploring whether polybutylene terephthalate (PBT) with improved flexibility can be utilized for the production of high strength and low modulus industrial yarn. In this study, a low velocity spinning multi-stage multi-ratio drawing technology route was employed for spinning, but PBT fibers only achieved a break strength of 5.1cN/dtex, which was lower than that of PET fibers (7.2cN/dtex). By comparing the multi-level structure evolution of PET and PBT during spinning, it was found that the core problem limiting the strength improvement of PBT fibers is due to the early formation of folded chain lamellar structure in PBT as-spun fibers during cooling, which hinders conformational transition during hot drawing and limits the drawing ratio. This has important implications for the development of PBT industrial yarn technology by adjusting the crystallization characteristics of PBT as-spun fibers.

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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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