Han-Xu Zhou, Ling-Chun Liu, De-Shuai Kong, Hua Yuan, Cong Du
{"title":"通过拉伸介导的网络工程,具有高机械性能和水稳定性的可生物降解海藻酸盐基纤维","authors":"Han-Xu Zhou, Ling-Chun Liu, De-Shuai Kong, Hua Yuan, Cong Du","doi":"10.1007/s10118-026-3671-0","DOIUrl":null,"url":null,"abstract":"<div><p>Seaweed polysaccharide-based fibers featuring incomparable merits, such as green fabrication procedures and intrinsic functionalities, are promising sustainable alternatives to petrochemical fibers that threaten both the ecological environment and human health. However, achieving simultaneously high strength, toughness, and stability of seaweed polysaccharide fibers remains a long-standing challenge owing to their low crystallinity and ionic crosslinks. Herein, we report a stretch-mediated network engineering strategy to overcome this limitation. Anisotropic architectures composed of dual-crosslinked sodium alginate and chemically crosslinked poly(vinyl alcohol) are prepared by pre-stretching. The highly ordered chemically crosslinked networks endow the fibers with high strength, and the anisotropic double networks prevent stress concentration and enable high toughness. The resultant fibers exhibit a tensile strength of 547.8 MPa, Young’s modulus of 17.6 GPa, and toughness of 43.3 MJ/m<sup>3</sup>, surpassing most regenerated biomass fibers. Additionally, fibers with an anisotropic network exhibit good aqueous stability, guaranteeing their usage in diverse solution environments and potential applications in triboelectric textiles. This study demonstrates a general and scalable strategy to decouple the strength–toughness trade-off in polysaccharide fibers without sacrificing biodegradability, thereby providing new insights into the structural design of robust, stable, and sustainable biomass-based fibers.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":517,"journal":{"name":"Chinese Journal of Polymer Science","volume":"44 8","pages":"2513 - 2523"},"PeriodicalIF":4.6000,"publicationDate":"2026-06-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Biodegradable Alginate-based Fibers with High Mechanical Performance and Aqueous Stability via Stretch-mediated Network Engineering\",\"authors\":\"Han-Xu Zhou, Ling-Chun Liu, De-Shuai Kong, Hua Yuan, Cong Du\",\"doi\":\"10.1007/s10118-026-3671-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Seaweed polysaccharide-based fibers featuring incomparable merits, such as green fabrication procedures and intrinsic functionalities, are promising sustainable alternatives to petrochemical fibers that threaten both the ecological environment and human health. However, achieving simultaneously high strength, toughness, and stability of seaweed polysaccharide fibers remains a long-standing challenge owing to their low crystallinity and ionic crosslinks. Herein, we report a stretch-mediated network engineering strategy to overcome this limitation. Anisotropic architectures composed of dual-crosslinked sodium alginate and chemically crosslinked poly(vinyl alcohol) are prepared by pre-stretching. The highly ordered chemically crosslinked networks endow the fibers with high strength, and the anisotropic double networks prevent stress concentration and enable high toughness. The resultant fibers exhibit a tensile strength of 547.8 MPa, Young’s modulus of 17.6 GPa, and toughness of 43.3 MJ/m<sup>3</sup>, surpassing most regenerated biomass fibers. Additionally, fibers with an anisotropic network exhibit good aqueous stability, guaranteeing their usage in diverse solution environments and potential applications in triboelectric textiles. This study demonstrates a general and scalable strategy to decouple the strength–toughness trade-off in polysaccharide fibers without sacrificing biodegradability, thereby providing new insights into the structural design of robust, stable, and sustainable biomass-based fibers.</p><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":517,\"journal\":{\"name\":\"Chinese Journal of Polymer Science\",\"volume\":\"44 8\",\"pages\":\"2513 - 2523\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2026-06-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chinese Journal of Polymer Science\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s10118-026-3671-0\",\"RegionNum\":2,\"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":"Chinese Journal of Polymer Science","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10118-026-3671-0","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Biodegradable Alginate-based Fibers with High Mechanical Performance and Aqueous Stability via Stretch-mediated Network Engineering
Seaweed polysaccharide-based fibers featuring incomparable merits, such as green fabrication procedures and intrinsic functionalities, are promising sustainable alternatives to petrochemical fibers that threaten both the ecological environment and human health. However, achieving simultaneously high strength, toughness, and stability of seaweed polysaccharide fibers remains a long-standing challenge owing to their low crystallinity and ionic crosslinks. Herein, we report a stretch-mediated network engineering strategy to overcome this limitation. Anisotropic architectures composed of dual-crosslinked sodium alginate and chemically crosslinked poly(vinyl alcohol) are prepared by pre-stretching. The highly ordered chemically crosslinked networks endow the fibers with high strength, and the anisotropic double networks prevent stress concentration and enable high toughness. The resultant fibers exhibit a tensile strength of 547.8 MPa, Young’s modulus of 17.6 GPa, and toughness of 43.3 MJ/m3, surpassing most regenerated biomass fibers. Additionally, fibers with an anisotropic network exhibit good aqueous stability, guaranteeing their usage in diverse solution environments and potential applications in triboelectric textiles. This study demonstrates a general and scalable strategy to decouple the strength–toughness trade-off in polysaccharide fibers without sacrificing biodegradability, thereby providing new insights into the structural design of robust, stable, and sustainable biomass-based fibers.
期刊介绍:
Chinese Journal of Polymer Science (CJPS) is a monthly journal published in English and sponsored by the Chinese Chemical Society and the Institute of Chemistry, Chinese Academy of Sciences. CJPS is edited by a distinguished Editorial Board headed by Professor Qi-Feng Zhou and supported by an International Advisory Board in which many famous active polymer scientists all over the world are included. The journal was first published in 1983 under the title Polymer Communications and has the current name since 1985.
CJPS is a peer-reviewed journal dedicated to the timely publication of original research ideas and results in the field of polymer science. The issues may carry regular papers, rapid communications and notes as well as feature articles. As a leading polymer journal in China published in English, CJPS reflects the new achievements obtained in various laboratories of China, CJPS also includes papers submitted by scientists of different countries and regions outside of China, reflecting the international nature of the journal.