{"title":"Hydrophilic Antistatic Modification: Preparation and Properties of Long-Chain Segment Copolymerized PET","authors":"Chaoyou Chen, Shuyang Li, Wangyang Xiao, Ben Wei, Xuzhen Zhang, Xiuhua Wang, Chongyin Zhang","doi":"10.1134/S1560090425600226","DOIUrl":null,"url":null,"abstract":"<p>To address the issue of poly(ethylene terephthalate) being highly hydrophobic and prone to static electricity due to friction, this study modifies PET through copolymerization with flexible long-chain monomers containing hydrophilic functional groups, creating a novel spinning-grade modified polyester with both hydrophilic and antistatic properties. Specifically, polyethylene glycol with a specific molecular weight (<i>M</i><sub>n</sub> = 4000) was used as a reactive hydrophilic and antistatic modification component, with a copolymerization content of 5~20%. Testing and characterization of the copolyester structure and properties showed that, compared to pure PET polyester, the introduction of hydrophilic ether bonds resulted in a significant hydrophilic modification effect, with the moisture absorption rate increasing from 0.11 to 1.12% and the surface water contact angle decreasing from 89.6° to 64.1°. Meanwhile, the volume resistivity of the copolyester decreased by 3–4 orders of magnitude compared to pure PET. This study improves the hydrophilic and antistatic properties of PET polyester through a low-cost modification method, providing essential reference for the development of functional polyesters and their fiber products.</p>","PeriodicalId":739,"journal":{"name":"Polymer Science, Series B","volume":"66 6","pages":"703 - 715"},"PeriodicalIF":1.0000,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Science, Series B","FirstCategoryId":"1","ListUrlMain":"https://link.springer.com/article/10.1134/S1560090425600226","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0
Abstract
To address the issue of poly(ethylene terephthalate) being highly hydrophobic and prone to static electricity due to friction, this study modifies PET through copolymerization with flexible long-chain monomers containing hydrophilic functional groups, creating a novel spinning-grade modified polyester with both hydrophilic and antistatic properties. Specifically, polyethylene glycol with a specific molecular weight (Mn = 4000) was used as a reactive hydrophilic and antistatic modification component, with a copolymerization content of 5~20%. Testing and characterization of the copolyester structure and properties showed that, compared to pure PET polyester, the introduction of hydrophilic ether bonds resulted in a significant hydrophilic modification effect, with the moisture absorption rate increasing from 0.11 to 1.12% and the surface water contact angle decreasing from 89.6° to 64.1°. Meanwhile, the volume resistivity of the copolyester decreased by 3–4 orders of magnitude compared to pure PET. This study improves the hydrophilic and antistatic properties of PET polyester through a low-cost modification method, providing essential reference for the development of functional polyesters and their fiber products.
期刊介绍:
Polymer Science, Series B is a journal published in collaboration with the Russian Academy of Sciences. Series B experimental and theoretical papers and reviews dealing with the synthesis, kinetics, catalysis, and chemical transformations of macromolecules, supramolecular structures, and polymer matrix-based composites (6 issues a year). All journal series present original papers and reviews covering all fundamental aspects of macromolecular science. Contributions should be of marked novelty and interest for a broad readership. Articles may be written in English or Russian regardless of country and nationality of authors. All manuscripts are peer reviewed