Synthesis of biodegradable PGA-PBC-PGA triblock copolymers and closed-loop recycling via a thermal depolymerization strategy

The emergence of biodegradable polymers has brought hope for solving the problem of plastic pollution. Chemical recovery of biodegradable polymers not only avoids CO 2 emissions from polyester degradation, but also enables sustainable utilization of feedstocks. In this study, biodegradable PGA-PBC-P...

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Veröffentlicht in:Green chemistry : an international journal and green chemistry resource : GC 2023-11, Vol.25 (23), p.9998-10009
Hauptverfasser: Wang, Yong, Wen, Liang, Liu, Jiajian, Li, Chuncheng, Zhang, Zijian, Xiao, Yaonan, Yin, Tian, Wu, Shaohua, Jiang, Zhikui, Zhang, Bo
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Sprache:eng
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Zusammenfassung:The emergence of biodegradable polymers has brought hope for solving the problem of plastic pollution. Chemical recovery of biodegradable polymers not only avoids CO 2 emissions from polyester degradation, but also enables sustainable utilization of feedstocks. In this study, biodegradable PGA-PBC-PGA triblock copolymers with chemical recovery characteristics were synthesized using ring-opening polymerization (ROP) of glycolide (GL). The T onset of the triblock copolymers was higher than 315 °C. Mechanical tests showed that the tensile strengths of the copolymers were in the range of 27.5–98.2 MPa, and the elongations at break were in the range of 9.2–409%. The gas permeation test showed that the triblock copolymers had excellent O 2 and CO 2 barrier performance, which was better than PBS, PBAT and PLA. Besides, the triblock copolymers have excellent degradation properties under both enzymatic and non-enzymatic conditions. What's more, the triblock copolymers were allowed to recover GL by thermal depolymerization. Among them, PGA-PBC-PGA60 could recover GL in 82% yield at 240 °C in 3 hours. The recovered GL could be reused for the next polymerization after recrystallization and purification. The performances of the copolymers after re-polymerization were comparable to that of the original copolymer, successfully completing the closed-loop process from a monomer to a polymer and then to a monomer.
ISSN:1463-9262
1463-9270
DOI:10.1039/D3GC03236A