{"title":"温度和应力双重作用下链取向和晶体结构的多尺度演化","authors":"Chengyao Liang, Weilei Huang, Senlong Yu, Qianqian Wang, Zexu Hu, Hengxue Xiang, Meifang Zhu","doi":"10.1021/acs.macromol.5c00686","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"7 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multiscale Evolution of Chain Orientation and Crystal Structure under the Dual Action of Temperature and Stress\",\"authors\":\"Chengyao Liang, Weilei Huang, Senlong Yu, Qianqian Wang, Zexu Hu, Hengxue Xiang, Meifang Zhu\",\"doi\":\"10.1021/acs.macromol.5c00686\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":51,\"journal\":{\"name\":\"Macromolecules\",\"volume\":\"7 1\",\"pages\":\"\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2025-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Macromolecules\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.macromol.5c00686\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecules","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.macromol.5c00686","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
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.
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.