高温增强氢键相关π -π杂化相互作用在杂环芳纶纤维辅助链自有序中的应用

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Boya Liu, Yiyang Chen, Qihong Zhang, Yuntian Lai, Ruke Lin, Longbo Luo, Junwei Lv* and Xiangyang Liu*, 
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引用次数: 0

摘要

本文发现了独特的分子间共振辅助氢键(RAHB)在高温下被激活,构建了异常热增强氢键相关的π -π杂化相互作用,并在纺丝芳纶纤维的自发有序中起着至关重要的作用。这种自发排序深刻地影响了芳纶纤维的取向和自伸长率,最终决定了芳纶纤维的高机械强度。此外,利用纺丝时芳纶纤维的温度依赖性弛豫特性,设计了一种具有可调张力的特定多阶段热拉伸策略,以匹配随着温度升高而不同的弛豫水平。具体来说,一种独特的无张力热处理工艺用于高温阶段,通过RAHB诱导纤维自有序。这种方法有效地防止了纤维在不同温度下过载,从而显著抑制了纳米级缺陷的传播,并生产出具有意想不到的高机械强度(>5.3 GPa)的芳纶纤维。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Abnormal High-Temperature-Enhanced Hydrogen Bond-Related π–π Hybrid Interaction in Heterocyclic Aramid Fiber-Assisted Chain Self-Ordering

Abnormal High-Temperature-Enhanced Hydrogen Bond-Related π–π Hybrid Interaction in Heterocyclic Aramid Fiber-Assisted Chain Self-Ordering

In this article, unique intermolecular resonance-assisted hydrogen bonding (RAHB) is found to be activated by high temperature, which constructs an abnormal thermal-enhanced hydrogen bond-related π–π hybrid interaction, and plays a crucial role in the spontaneous ordering of the as-spun aramid fiber. This spontaneous ordering profoundly influences the orientation and self-elongation within aramid fiber, ultimately determining their high mechanical strength. Additionally, utilizing the temperature-dependent relaxation characterization of the as-spun aramid fiber, a specific multistage thermal stretching strategy with tunable tension was then designed to match different relaxation levels as the temperature increased. Specifically, a unique tension-free heat treatment procedure was intended for the high-temperature stage, which induces fiber self-ordering through RAHB. This approach effectively prevents fiber overloading across various temperatures, thereby significantly inhibiting the propagation of nanosized defects and producing aramid fiber with unexpectedly high mechanical strength (>5.3 GPa).

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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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