Boya Liu, Yiyang Chen, Qihong Zhang, Yuntian Lai, Ruke Lin, Longbo Luo, Junwei Lv* and Xiangyang Liu*,
{"title":"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","authors":"Boya Liu, Yiyang Chen, Qihong Zhang, Yuntian Lai, Ruke Lin, Longbo Luo, Junwei Lv* and Xiangyang Liu*, ","doi":"10.1021/acs.macromol.5c00889","DOIUrl":null,"url":null,"abstract":"<p >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).</p>","PeriodicalId":51,"journal":{"name":"Macromolecules","volume":"58 14","pages":"7104–7111"},"PeriodicalIF":5.2000,"publicationDate":"2025-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Abnormal High-Temperature-Enhanced Hydrogen Bond-Related π–π Hybrid Interaction in Heterocyclic Aramid Fiber-Assisted Chain Self-Ordering\",\"authors\":\"Boya Liu, Yiyang Chen, Qihong Zhang, Yuntian Lai, Ruke Lin, Longbo Luo, Junwei Lv* and Xiangyang Liu*, \",\"doi\":\"10.1021/acs.macromol.5c00889\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >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).</p>\",\"PeriodicalId\":51,\"journal\":{\"name\":\"Macromolecules\",\"volume\":\"58 14\",\"pages\":\"7104–7111\"},\"PeriodicalIF\":5.2000,\"publicationDate\":\"2025-06-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Macromolecules\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.macromol.5c00889\",\"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://pubs.acs.org/doi/10.1021/acs.macromol.5c00889","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
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).
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.