Drawing-Induced Crimp Formation and Wettability of Four-Lobed Side-by-Side PBT/PET Bicomponent Fibers.

IF 4.9 3区 工程技术 Q1 POLYMER SCIENCE
Polymers Pub Date : 2025-09-18 DOI:10.3390/polym17182529
Xinkang Xu, Pei Feng, Zexu Hu, Jiazheng Wang, Qianchun Xu, Chongchang Yang
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引用次数: 0

Abstract

PBT/PET side-by-side bicomponent fibers form helical crimp structures under thermal or mechanical stress, though the mechanism behind mechanically induced crimping remains unclear. In this study, four-lobed cross-sectional PBT/PET side-by-side bicomponent fibers were produced and subjected to drawing from 1.6 to 4.0 times at 80 °C to induce crimping. Increasing draw ratios significantly enhanced fiber tenacity (from 0.64 to 3.91 cN/dtex) and reduced crimp radius (from 2.05 mm to 0.64 mm). A predictive crimp curvature model integrating Denton's crimp theory and a four-element viscoelastic model was established, with corrected results achieving an R2 of 0.9951. Additionally, four-lobed fibers showed better wettability, with a static contact angle 3.56° lower than that of circular fibers. This work provides theoretical guidance for high-performance self-crimping fiber design.

四叶并列PBT/PET双组分纤维的拉伸诱导卷曲形成和润湿性。
PBT/PET并排双组分纤维在热应力或机械应力下形成螺旋卷曲结构,但机械诱导卷曲背后的机制尚不清楚。在本研究中,生产了四叶截面PBT/PET并排双组分纤维,并在80°C下拉伸1.6至4.0次以诱导卷曲。增加拉伸比可以显著提高纤维的韧性(从0.64增加到3.91 cN/dtex),减小卷曲半径(从2.05 mm减少到0.64 mm)。结合Denton卷曲理论和四元粘弹性模型,建立了预测卷曲曲率模型,修正后的R2为0.9951。此外,四叶纤维的润湿性更好,其静态接触角比圆形纤维小3.56°。该研究为高性能自卷曲光纤的设计提供了理论指导。
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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来源期刊
Polymers
Polymers POLYMER SCIENCE-
CiteScore
8.00
自引率
16.00%
发文量
4697
审稿时长
1.3 months
期刊介绍: Polymers (ISSN 2073-4360) is an international, open access journal of polymer science. It publishes research papers, short communications and review papers. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Polymers provides an interdisciplinary forum for publishing papers which advance the fields of (i) polymerization methods, (ii) theory, simulation, and modeling, (iii) understanding of new physical phenomena, (iv) advances in characterization techniques, and (v) harnessing of self-assembly and biological strategies for producing complex multifunctional structures.
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