多种氢键3D打印弹性体,光热双固化增强增韧,可定制仿生柔性夹具

IF 18.5 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Tongyi Wu, Qiaoling Zhang, Zhiwei Zhang, Taojun Lin, Zhongbiao Xie, Yiquan Zang, Xingyan Zheng, Long Chen, Haisheng Hu, Qiu Chen, Guoqiao Lai
{"title":"多种氢键3D打印弹性体,光热双固化增强增韧,可定制仿生柔性夹具","authors":"Tongyi Wu, Qiaoling Zhang, Zhiwei Zhang, Taojun Lin, Zhongbiao Xie, Yiquan Zang, Xingyan Zheng, Long Chen, Haisheng Hu, Qiu Chen, Guoqiao Lai","doi":"10.1002/adfm.202510489","DOIUrl":null,"url":null,"abstract":"This study develops low‐viscosity, two‐component polycaprolactone (PCL)‐based 3D‐printed elastomers via photothermal dual curing. To prevent a sudden increase in viscosity from the direct introduction of hydrogen bonding in the oligomer, multiple hydrogen bonding components are innovatively added into the resin system in the form of the chain extender 12NH. The samples undergo thermal treatment after light curing. Incorporating 12NH, which retains unreacted isocyanate functionality, into the elastomer's macromolecular long‐chain forms an interpenetrating network of multiple hydrogen bonds, dynamic covalent bonds, and a micro‐phase separation. The resultant elastomers exhibit superior mechanical properties, achieving a tensile strength of 43.5 MPa and tensile toughness of 213.1 MJ m<jats:sup>−3</jats:sup>, while maintaining high biocompatibility. These properties surpass those of existing PCL‐based reduced photopolymerized 3D‐printed elastomers. Subsequently, complex lattice structures and bionic flexible grippers are successfully printed, validating their potential in applications requiring efficient gripping and rapid response. This study offers novel concepts for designing 3D‐printed elastomers that optimize the balance between high strength and toughness, precision molding, and biosafety, facilitating the development of tailored manufacturing for flexible robotics and implantable medical devices.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"6 1","pages":""},"PeriodicalIF":18.5000,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multiple Hydrogen Bonded 3D‐Printed Elastomers with Enhanced Toughening by Photothermal Dual Curing for Customizable Biomimetic Flexible Grippers\",\"authors\":\"Tongyi Wu, Qiaoling Zhang, Zhiwei Zhang, Taojun Lin, Zhongbiao Xie, Yiquan Zang, Xingyan Zheng, Long Chen, Haisheng Hu, Qiu Chen, Guoqiao Lai\",\"doi\":\"10.1002/adfm.202510489\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"This study develops low‐viscosity, two‐component polycaprolactone (PCL)‐based 3D‐printed elastomers via photothermal dual curing. To prevent a sudden increase in viscosity from the direct introduction of hydrogen bonding in the oligomer, multiple hydrogen bonding components are innovatively added into the resin system in the form of the chain extender 12NH. The samples undergo thermal treatment after light curing. Incorporating 12NH, which retains unreacted isocyanate functionality, into the elastomer's macromolecular long‐chain forms an interpenetrating network of multiple hydrogen bonds, dynamic covalent bonds, and a micro‐phase separation. The resultant elastomers exhibit superior mechanical properties, achieving a tensile strength of 43.5 MPa and tensile toughness of 213.1 MJ m<jats:sup>−3</jats:sup>, while maintaining high biocompatibility. These properties surpass those of existing PCL‐based reduced photopolymerized 3D‐printed elastomers. Subsequently, complex lattice structures and bionic flexible grippers are successfully printed, validating their potential in applications requiring efficient gripping and rapid response. This study offers novel concepts for designing 3D‐printed elastomers that optimize the balance between high strength and toughness, precision molding, and biosafety, facilitating the development of tailored manufacturing for flexible robotics and implantable medical devices.\",\"PeriodicalId\":112,\"journal\":{\"name\":\"Advanced Functional Materials\",\"volume\":\"6 1\",\"pages\":\"\"},\"PeriodicalIF\":18.5000,\"publicationDate\":\"2025-07-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Advanced Functional Materials\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/adfm.202510489\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202510489","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

本研究通过光热双固化技术开发了低粘度、双组分聚己内酯(PCL)基3D打印弹性体。为了防止在低聚物中直接引入氢键而导致粘度突然增加,在树脂体系中创新性地添加了多种氢键组分,以扩链剂12NH的形式。样品在光固化后进行热处理。将保留未反应异氰酸酯功能的12NH加入弹性体的大分子长链中,形成多个氢键、动态共价键和微相分离的互穿网络。合成的弹性体具有优异的力学性能,抗拉强度为43.5 MPa,抗拉韧性为213.1 MJ m−3,同时保持较高的生物相容性。这些性能超过了现有的基于PCL的还原光聚合3D打印弹性体。随后,复杂的晶格结构和仿生柔性夹具被成功打印,验证了它们在需要高效抓取和快速响应的应用中的潜力。该研究为设计3D打印弹性体提供了新的概念,优化了高强度和韧性,精密成型和生物安全性之间的平衡,促进了柔性机器人和植入式医疗设备定制制造的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiple Hydrogen Bonded 3D‐Printed Elastomers with Enhanced Toughening by Photothermal Dual Curing for Customizable Biomimetic Flexible Grippers
This study develops low‐viscosity, two‐component polycaprolactone (PCL)‐based 3D‐printed elastomers via photothermal dual curing. To prevent a sudden increase in viscosity from the direct introduction of hydrogen bonding in the oligomer, multiple hydrogen bonding components are innovatively added into the resin system in the form of the chain extender 12NH. The samples undergo thermal treatment after light curing. Incorporating 12NH, which retains unreacted isocyanate functionality, into the elastomer's macromolecular long‐chain forms an interpenetrating network of multiple hydrogen bonds, dynamic covalent bonds, and a micro‐phase separation. The resultant elastomers exhibit superior mechanical properties, achieving a tensile strength of 43.5 MPa and tensile toughness of 213.1 MJ m−3, while maintaining high biocompatibility. These properties surpass those of existing PCL‐based reduced photopolymerized 3D‐printed elastomers. Subsequently, complex lattice structures and bionic flexible grippers are successfully printed, validating their potential in applications requiring efficient gripping and rapid response. This study offers novel concepts for designing 3D‐printed elastomers that optimize the balance between high strength and toughness, precision molding, and biosafety, facilitating the development of tailored manufacturing for flexible robotics and implantable medical devices.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信