{"title":"由间苯二酚环氧单体和酸酐制备的生物基环氧树脂","authors":"Angela Marotta , Cosimo Brondi , Mattia Sivero , Pierfrancesco Cerruti , Veronica Ambrogi , Alice Mija","doi":"10.1016/j.mtsust.2025.101212","DOIUrl":null,"url":null,"abstract":"<div><div>Design and development of high glass transition (<em>T</em><sub><em>g</em></sub>) biobased epoxy thermosets is a key challenge for several fields of applications. To this aim, in the present study diglycidyl ether of resorcinol (DGER) is proposed as a potentially biobased alternative to diglycidyl ether of bisphenol A (DGEBA) for the synthesis of high-performance epoxy resins. DGER is obtained by diglycidylation of resorcinol, an aromatic diol synthesized by fermentation of glucose or catechin. The curing process of DGER in the presence of various anhydrides as hardeners and several imidazole initiators is studied. The most efficient hardener/initiatior combination, which leads to the resin with the highest degree of reaction conversion and the highest glass transition (<em>T</em><sub><em>g</em></sub> > 100 °C) is further studied by chemorheological analysis, and a kinetic model for the crosslinking reaction is proposed. The conversion degree is evaluated by monitoring the disappearing of characteristic peaks of anhydride and epoxy rings in ATR-FTIR spectra collected at different curing temperature, as well as the appearance of the characteristic band of ester groups typically formed in epoxy/anhydride resins. By fitting the conversion data, the autocatalytic crosslinking mechanism is confirmed, and kinetic parameters are calculated. Also, the thermomechanical characteristics and chemical stability of DGER-based epoxy resins are evaluated, confirming the potential use of this epoxy thermosets when high mechanical and thermal properties are required.</div></div>","PeriodicalId":18322,"journal":{"name":"Materials Today Sustainability","volume":"31 ","pages":"Article 101212"},"PeriodicalIF":7.9000,"publicationDate":"2025-08-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Biobased epoxy resins obtained from resorcinol epoxy monomer and anhydrides\",\"authors\":\"Angela Marotta , Cosimo Brondi , Mattia Sivero , Pierfrancesco Cerruti , Veronica Ambrogi , Alice Mija\",\"doi\":\"10.1016/j.mtsust.2025.101212\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Design and development of high glass transition (<em>T</em><sub><em>g</em></sub>) biobased epoxy thermosets is a key challenge for several fields of applications. To this aim, in the present study diglycidyl ether of resorcinol (DGER) is proposed as a potentially biobased alternative to diglycidyl ether of bisphenol A (DGEBA) for the synthesis of high-performance epoxy resins. DGER is obtained by diglycidylation of resorcinol, an aromatic diol synthesized by fermentation of glucose or catechin. The curing process of DGER in the presence of various anhydrides as hardeners and several imidazole initiators is studied. The most efficient hardener/initiatior combination, which leads to the resin with the highest degree of reaction conversion and the highest glass transition (<em>T</em><sub><em>g</em></sub> > 100 °C) is further studied by chemorheological analysis, and a kinetic model for the crosslinking reaction is proposed. The conversion degree is evaluated by monitoring the disappearing of characteristic peaks of anhydride and epoxy rings in ATR-FTIR spectra collected at different curing temperature, as well as the appearance of the characteristic band of ester groups typically formed in epoxy/anhydride resins. By fitting the conversion data, the autocatalytic crosslinking mechanism is confirmed, and kinetic parameters are calculated. Also, the thermomechanical characteristics and chemical stability of DGER-based epoxy resins are evaluated, confirming the potential use of this epoxy thermosets when high mechanical and thermal properties are required.</div></div>\",\"PeriodicalId\":18322,\"journal\":{\"name\":\"Materials Today Sustainability\",\"volume\":\"31 \",\"pages\":\"Article 101212\"},\"PeriodicalIF\":7.9000,\"publicationDate\":\"2025-08-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Materials Today Sustainability\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2589234725001411\",\"RegionNum\":3,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Today Sustainability","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2589234725001411","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY","Score":null,"Total":0}
Biobased epoxy resins obtained from resorcinol epoxy monomer and anhydrides
Design and development of high glass transition (Tg) biobased epoxy thermosets is a key challenge for several fields of applications. To this aim, in the present study diglycidyl ether of resorcinol (DGER) is proposed as a potentially biobased alternative to diglycidyl ether of bisphenol A (DGEBA) for the synthesis of high-performance epoxy resins. DGER is obtained by diglycidylation of resorcinol, an aromatic diol synthesized by fermentation of glucose or catechin. The curing process of DGER in the presence of various anhydrides as hardeners and several imidazole initiators is studied. The most efficient hardener/initiatior combination, which leads to the resin with the highest degree of reaction conversion and the highest glass transition (Tg > 100 °C) is further studied by chemorheological analysis, and a kinetic model for the crosslinking reaction is proposed. The conversion degree is evaluated by monitoring the disappearing of characteristic peaks of anhydride and epoxy rings in ATR-FTIR spectra collected at different curing temperature, as well as the appearance of the characteristic band of ester groups typically formed in epoxy/anhydride resins. By fitting the conversion data, the autocatalytic crosslinking mechanism is confirmed, and kinetic parameters are calculated. Also, the thermomechanical characteristics and chemical stability of DGER-based epoxy resins are evaluated, confirming the potential use of this epoxy thermosets when high mechanical and thermal properties are required.
期刊介绍:
Materials Today Sustainability is a multi-disciplinary journal covering all aspects of sustainability through materials science.
With a rapidly increasing population with growing demands, materials science has emerged as a critical discipline toward protecting of the environment and ensuring the long term survival of future generations.