4.6 Article

Degradation of Thermal-Mechanically Stable Epoxy Thermosets, Recycling of Carbon Fiber, and Reapplication of the Degraded Products

期刊

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
卷 9, 期 15, 页码 5304-5314

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.0c08998

关键词

self-curing; eugenol-based epoxy; thermal-mechanically stable epoxy networks; aminolysis degradation; catalyst-free; reapplication of the degraded products; recycling of carbon fiber

资金

  1. Advanced Research Center For Green Materials Science and Technology from The Featured Area Research Center Program within Ministry of Education [109L9006]
  2. Ministry of Science and Technology in Taiwan [MOST 109-2634-F-002-042, 107-2221-E-005-025-MY3]

向作者/读者索取更多资源

The research focuses on the degradability of two thermal-mechanically stable epoxy networks derived from self-curing of eugenol-based epoxy resins, as well as the recycling of carbon fibers in epoxy/carbon fiber composites. The study demonstrates the successful degradation and reapplication of thermal-mechanically stable epoxy networks, showing promise for industrial applications and environmental sustainability.
Conventional epoxy resins can meet the requirement for engineering applications in which high glass transition and thermal stability are essential, but they show no degradability or recyclability. Vitrimers, with covalent adaptable networks, provide reprocessability and degradability. However, the thermally activated bond-exchange reactions prevent the composites from being thermal-mechanically stable at high temperatures. Therefore, developing epoxy/carbon fiber composites with thermal stability and degradability is attractive for industrial applications and environmental sustainability. In this work, we report the degradability of two thermal-mechanically stable epoxy networks derived from self-curing of two eugenol-based epoxy resins: bis(2-methoxy-4-(oxiran-2-ylmethyl)phenyl) succinate (II) and tris(2-methoxy-4-(oxiran-2-ylmethyl)phenyl)benzene-1,3,5-tricarboxylate (III). Degradation can be proceeded through aminolysis of aliphatic esters in the networks at a mild condition. The exact structures of degraded products were precisely analyzed by H-1 NMR spectra. An epoxy/carbon fiber composite based on III/carbon fiber was prepared. After degrading the epoxy network, the carbon fiber was recycled. Scanning electron microscopy (SEM) pictures show that the recycled carbon fiber is intact and looks the same as the virgin one. Furthermore, we modified the degraded product of epoxy networks for reapplication. One of the degraded products, oligo(1-oxy-3-(3-methoxy-4-phenylene)propan-2-ol) (IIc), was further reacted with methacrylic anhydride to obtain oligo(1-oxy-3-(3-methoxy-4-phenylene)propan-2-methacrylate) (IId). IId was further thermally cross-linked to a thermoset (IIe) with a T-g value of 170 degrees C. The successful degradation and reapplication of thermal-mechanically stable epoxy networks and the recycling of carbon fibers are well demonstrated.

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