{"title":"聚对苯二甲酸丁二酯- co -2,6-萘二酸酯共聚酯熔融纺纤维的拉伸和结晶行为","authors":"Hsu-I Mao, Wen-Tzu Wu, Jui-Yang Chou, Chin-Wen Chen","doi":"10.1002/pol.20240912","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>In this study, a series of poly(butylene terephthalate-co-2,6-naphthalate) (PBTN) copolymers was synthesized via a one-step polycondensation process. These PBTN copolymers demonstrate excellent thermal stability and semi-crystalline behavior, with the enthalpy of melting values exceeding 17 J g<sup>−1</sup>. Crystallization kinetics analysis revealed that the copolymers exhibit significantly higher crystallization rates than neat poly(butylene terephthalate) (PBT) and poly(butylene naphthalate) (PBN), making them well-suited for fiber production. The copolymers were melt-spun, followed by a post-drawing process at a ratio of 2.0, to enhance fiber strength. By adjusting the 2,6-naphthalene dicarboxylate (NDC) content, the mechanical properties and crystallinity of the PBTN fibers were fine-tuned. Tensile testing revealed that the copolymer fiber containing 50 mol% NDC, post-drawn at a ratio of 2.0, exhibits superior toughness, with maximum tenacity and elongation values of 3.13 g den<sup>−1</sup> and 69.3%, respectively.</p>\n </div>","PeriodicalId":16888,"journal":{"name":"Journal of Polymer Science","volume":"63 3","pages":"554-565"},"PeriodicalIF":3.9000,"publicationDate":"2024-11-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Tensile and Crystallization Behavior of Melt-Spun Fibers Derived From Poly(Butylene Terephthalate-Co-2,6-Naphthalate) Copolyester\",\"authors\":\"Hsu-I Mao, Wen-Tzu Wu, Jui-Yang Chou, Chin-Wen Chen\",\"doi\":\"10.1002/pol.20240912\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>In this study, a series of poly(butylene terephthalate-co-2,6-naphthalate) (PBTN) copolymers was synthesized via a one-step polycondensation process. These PBTN copolymers demonstrate excellent thermal stability and semi-crystalline behavior, with the enthalpy of melting values exceeding 17 J g<sup>−1</sup>. Crystallization kinetics analysis revealed that the copolymers exhibit significantly higher crystallization rates than neat poly(butylene terephthalate) (PBT) and poly(butylene naphthalate) (PBN), making them well-suited for fiber production. The copolymers were melt-spun, followed by a post-drawing process at a ratio of 2.0, to enhance fiber strength. By adjusting the 2,6-naphthalene dicarboxylate (NDC) content, the mechanical properties and crystallinity of the PBTN fibers were fine-tuned. Tensile testing revealed that the copolymer fiber containing 50 mol% NDC, post-drawn at a ratio of 2.0, exhibits superior toughness, with maximum tenacity and elongation values of 3.13 g den<sup>−1</sup> and 69.3%, respectively.</p>\\n </div>\",\"PeriodicalId\":16888,\"journal\":{\"name\":\"Journal of Polymer Science\",\"volume\":\"63 3\",\"pages\":\"554-565\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2024-11-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Polymer Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/pol.20240912\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Polymer Science","FirstCategoryId":"92","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/pol.20240912","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
摘要
本研究采用一步缩聚法合成了一系列聚对苯二甲酸丁二酯-co-2,6-萘二酸酯(PBTN)共聚物。这些PBTN共聚物表现出优异的热稳定性和半结晶行为,熔融焓值超过17 J g−1。结晶动力学分析表明,该共聚物的结晶速率明显高于纯聚对苯二甲酸丁二酯(PBT)和聚萘二甲酸丁二酯(PBN),非常适合用于纤维生产。共聚物熔融纺丝,然后以2.0的比例进行后拉伸,以提高纤维强度。通过调节2,6-萘二羧酸盐(NDC)的含量,对PBTN纤维的力学性能和结晶度进行了微调。拉伸试验表明,NDC含量为50 mol%,后拉伸比例为2.0的共聚物纤维具有优异的韧性,最大韧性和伸长率分别为3.13 g den−1和69.3%。
Tensile and Crystallization Behavior of Melt-Spun Fibers Derived From Poly(Butylene Terephthalate-Co-2,6-Naphthalate) Copolyester
In this study, a series of poly(butylene terephthalate-co-2,6-naphthalate) (PBTN) copolymers was synthesized via a one-step polycondensation process. These PBTN copolymers demonstrate excellent thermal stability and semi-crystalline behavior, with the enthalpy of melting values exceeding 17 J g−1. Crystallization kinetics analysis revealed that the copolymers exhibit significantly higher crystallization rates than neat poly(butylene terephthalate) (PBT) and poly(butylene naphthalate) (PBN), making them well-suited for fiber production. The copolymers were melt-spun, followed by a post-drawing process at a ratio of 2.0, to enhance fiber strength. By adjusting the 2,6-naphthalene dicarboxylate (NDC) content, the mechanical properties and crystallinity of the PBTN fibers were fine-tuned. Tensile testing revealed that the copolymer fiber containing 50 mol% NDC, post-drawn at a ratio of 2.0, exhibits superior toughness, with maximum tenacity and elongation values of 3.13 g den−1 and 69.3%, respectively.
期刊介绍:
Journal of Polymer Research provides a forum for the prompt publication of articles concerning the fundamental and applied research of polymers. Its great feature lies in the diversity of content which it encompasses, drawing together results from all aspects of polymer science and technology.
As polymer research is rapidly growing around the globe, the aim of this journal is to establish itself as a significant information tool not only for the international polymer researchers in academia but also for those working in industry. The scope of the journal covers a wide range of the highly interdisciplinary field of polymer science and technology.