Xiangyu Zhou, Zhen Yu, Yajin Fang, Hongyun Hu, Songyue Cheng, Zhaobin Tang and Yanlin Liu
{"title":"High-performance fully bio-based dynamic covalent supramolecular epoxy resin: synthesis and properties†","authors":"Xiangyu Zhou, Zhen Yu, Yajin Fang, Hongyun Hu, Songyue Cheng, Zhaobin Tang and Yanlin Liu","doi":"10.1039/D4GC06425A","DOIUrl":null,"url":null,"abstract":"<p >Bio-based dynamic covalent thermosets have attracted widespread attention due to their potential to reduce dependence on fossil resources and address recycling issues after disposal. However, a longstanding challenge has been reconciling the use of bio-based raw materials with high-performance properties. To address this issue, we designed a method for preparing a fully bio-based dynamic covalent supramolecular epoxy resin, utilizing the reactive carbonyl and carboxyl groups of levulinic acid. Even with a relatively low crosslinking density (3152 mol m<small><sup>−3</sup></small>), the resin exhibits a glass transition temperature (<em>T</em><small><sub>g</sub></small>) of 164 °C, tensile strength of 111 MPa, and tensile modulus of 1864 MPa. In comparison, a resin cured with the commercial hardener DDM, which has a crosslinking density of 8855 mol m<small><sup>−3</sup></small>, displays a <em>T</em><small><sub>g</sub></small> of 167 °C, tensile strength of 86 MPa, and tensile modulus of 1278 MPa. Furthermore, the resin demonstrates reprocessability without the need for a catalyst. Benefiting from the dynamic effects of ester bonds within the network, the closed-loop chemical recovery of resin was confirmed. Additionally, the resin can be degraded in an alkaline environment, allowing for the recovery of the starting monomer, furandimethyl acid. This high-performance bio-based material is easy to synthesize and can be closed-loop recycled, providing a new strategy for the green development of high-performance thermosets.</p>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":" 12","pages":" 3248-3260"},"PeriodicalIF":9.3000,"publicationDate":"2025-03-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/gc/d4gc06425a","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Bio-based dynamic covalent thermosets have attracted widespread attention due to their potential to reduce dependence on fossil resources and address recycling issues after disposal. However, a longstanding challenge has been reconciling the use of bio-based raw materials with high-performance properties. To address this issue, we designed a method for preparing a fully bio-based dynamic covalent supramolecular epoxy resin, utilizing the reactive carbonyl and carboxyl groups of levulinic acid. Even with a relatively low crosslinking density (3152 mol m−3), the resin exhibits a glass transition temperature (Tg) of 164 °C, tensile strength of 111 MPa, and tensile modulus of 1864 MPa. In comparison, a resin cured with the commercial hardener DDM, which has a crosslinking density of 8855 mol m−3, displays a Tg of 167 °C, tensile strength of 86 MPa, and tensile modulus of 1278 MPa. Furthermore, the resin demonstrates reprocessability without the need for a catalyst. Benefiting from the dynamic effects of ester bonds within the network, the closed-loop chemical recovery of resin was confirmed. Additionally, the resin can be degraded in an alkaline environment, allowing for the recovery of the starting monomer, furandimethyl acid. This high-performance bio-based material is easy to synthesize and can be closed-loop recycled, providing a new strategy for the green development of high-performance thermosets.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.