解聚
聚碳酸酯
双酚A
乳酸
聚合物
化学
催化作用
烷基
有机化学
聚酯纤维
材料科学
化学工程
高分子化学
环氧树脂
细菌
工程类
生物
遗传学
作者
Arianna Brandolese,M. Edge,Neha Yadav,Ali Al Rida Hmayed,Andrew P. Dove
标识
DOI:10.1002/cssc.202500420
摘要
Mechanical recycling methods are a simple and effective approach to recycling plastics, but they often result in a direct reduction in the quality of the virgin polymer. Alternatively, chemical recycling of plastic waste provides a closed‐loop pathway that could offer a solution to the current end‐of‐life mismanagement of plastics. However, harsh reaction conditions, scalability, and product purification can limit the applicability of this process on a large scale. Here, an organocatalysed continuous flow depolymerization strategy is proposed for two soluble, commonly used plastics, poly(lactic acid) (PLA) and bisphenol A polycarbonate (BPA‐PC). This process used glycolysis to upcycle PLA to alkyl lactate and BPA‐PC to bisphenol A and ethylene carbonate under mild reaction conditions (up to 60 ⁰C). The complete depolymerization of both polymers was initially performed under batch conditions, allowing the solvents and catalysts to be screened. The process was further extended under continuous flow to explore catalyst stability and process scalability. Finally, it was demonstrated that alkyl lactate, bisphenol A and ethylene carbonate can be produced from waste polycarbonate and PLA, thus providing safe and economical access to these species through continuous flow depolymerization of plastic waste.
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