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Carbon fiber-reinforced epoxy with 100% fiber recycling by transesterification reactions

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Carbon fiber (CF)-reinforced epoxy is the most commonly used advanced composite with high performance. However, these composites usually face intractable disposal problems in their lifecycles, due to the stable cross-linked network structures of epoxy. To address this dilemma, this work proposes a facile yet efficient strategy for recycling carbon fibers from traditional carbon fiber-reinforced epoxy composites using epoxy–anhydride systems as a matrix. Diglycidyl ester of aliphatic cyclo (DGEAC) and methylhexahydrophthalic anhydride (MHHPA) were used as matrix, while T300 woven carbon fiber was used as reinforcement, to construct the composites CF/DGEAC/MHHPA. The epoxy matrix exhibited a high glass transition temperature (Tg = 126°C), high decomposition temperature (Td5 = 300°C), and good solvent resistance. By using 1,5,7-triazabicyclo[4.4.0]dec-5-ene (TBD) as a catalyst, the DGEAC/MHHPA networks could be degraded completely in ethylene glycol (EG) at 180°C within 6 h because of transesterification reactions between EG and the networks. Taking advantage of this result, a fiber recycling process was developed for carbon fiber composites, where the cross-linked networks of epoxy could be degraded with 100% carbon fiber recycling. Furthermore, the recycled carbon fiber maintained nearly 100% similarity in surface microscopic morphology and chemical structure compared with virgin carbon fiber. This work proposes a simple and efficient strategy for recycling carbon fiber from traditional high-performance composites, offering a convenient concept for the cyclic utilization of advanced composites.
Title: Carbon fiber-reinforced epoxy with 100% fiber recycling by transesterification reactions
Description:
Carbon fiber (CF)-reinforced epoxy is the most commonly used advanced composite with high performance.
However, these composites usually face intractable disposal problems in their lifecycles, due to the stable cross-linked network structures of epoxy.
To address this dilemma, this work proposes a facile yet efficient strategy for recycling carbon fibers from traditional carbon fiber-reinforced epoxy composites using epoxy–anhydride systems as a matrix.
Diglycidyl ester of aliphatic cyclo (DGEAC) and methylhexahydrophthalic anhydride (MHHPA) were used as matrix, while T300 woven carbon fiber was used as reinforcement, to construct the composites CF/DGEAC/MHHPA.
The epoxy matrix exhibited a high glass transition temperature (Tg = 126°C), high decomposition temperature (Td5 = 300°C), and good solvent resistance.
By using 1,5,7-triazabicyclo[4.
4.
0]dec-5-ene (TBD) as a catalyst, the DGEAC/MHHPA networks could be degraded completely in ethylene glycol (EG) at 180°C within 6 h because of transesterification reactions between EG and the networks.
Taking advantage of this result, a fiber recycling process was developed for carbon fiber composites, where the cross-linked networks of epoxy could be degraded with 100% carbon fiber recycling.
Furthermore, the recycled carbon fiber maintained nearly 100% similarity in surface microscopic morphology and chemical structure compared with virgin carbon fiber.
This work proposes a simple and efficient strategy for recycling carbon fiber from traditional high-performance composites, offering a convenient concept for the cyclic utilization of advanced composites.

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