温度和应力双重作用下链取向和晶体结构的多尺度演化

IF 5.1 1区 化学 Q1 POLYMER SCIENCE
Chengyao Liang, Weilei Huang, Senlong Yu, Qianqian Wang, Zexu Hu, Hengxue Xiang, Meifang Zhu
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引用次数: 0

摘要

全面了解聚酰胺形成过程中控制纤维性能的多尺度结构演变对高强纤维的理论发展至关重要。本研究系统研究了高强度聚酰胺66纤维(H-PA66F)在高速纺丝过程中关键阶段的分层结构转变,重点研究了分子链构象、氢键网络、晶体组织、取向动力学和长周期结构特征。通过构建三相结构模型,阐明了纤维加工过程中结构-性能的递进关系。在整个成型过程中观察到的力学增强归因于同步的结构优化:热拉伸通过晶体完善提高纤维强度,增加刚性段的对齐,而随后的热定型通过减少缺陷来稳定结构。这些发现建立了一个强大的结构-性能框架,为高性能聚酰胺纤维的目标多尺度结构工程提供了理论见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Multiscale Evolution of Chain Orientation and Crystal Structure under the Dual Action of Temperature and Stress

Multiscale Evolution of Chain Orientation and Crystal Structure under the Dual Action of Temperature and Stress
A comprehensive understanding of the multiscale structural evolution that governs fiber properties during polyamide formation is essential for the theoretical development of high-strength fibers. This study systematically investigates the hierarchical structural transformations in high-strength polyamide 66 fibers (H-PA66F) at key stages during high-speed spinning, with a focus on molecular chain conformations, hydrogen bonding networks, crystalline organization, orientation dynamics, and long-period structural features. By constructing a three-phase structural model, the study elucidates the progressive structural-property relationships during fiber processing. The mechanical enhancement observed throughout the formation process is attributed to synchronized structural optimizations: hot drawing enhances fiber strength through crystal perfection and increases the alignment of rigid segments, while subsequent heat setting stabilizes the structure by reducing defects. These findings establish a robust structure-performance framework, providing theoretical insights for the targeted multiscale structural engineering of high-performance polyamide fibers.
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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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