聚乙烯
聚氯乙烯
光催化
甲烷氧化偶联
聚丙烯
材料科学
激进的
废物管理
有机化学
化学工程
催化作用
化学
工程类
作者
Hao Chen,Kai Zheng,Qingxia Chen,Xiaodong Li,Yamin Li,Weiwei Shao,Jiaqi Xu,Junfa Zhu,Yang Pan,Yongfu Sun,Yi Xie
标识
DOI:10.1002/anie.201915766
摘要
Abstract Reported here is the first highly selective conversion of various waste plastics into C 2 fuels under simulated natural environment conditions by a sequential photoinduced C−C cleavage and coupling pathway, where single‐use bags, disposable food containers, food wrap films, and their main components of polyethylene, polypropylene, and polyvinyl chloride can be photocatalytically transformed into CH 3 COOH without using sacrificial agents. As an example, polyethylene is photodegraded 100 % into CO 2 within 40 h by single‐unit‐cell thick Nb 2 O 5 layers, while the produced CO 2 is further photoreduced to CH 3 COOH. Various methods and experiments disclose that O 2 and . OH radicals trigger the oxidative C−C cleavage of polyethylene to form CO 2 , while other investigations show that the yielded CH 3 COOH stems from CO 2 photoreduction by C−C coupling of . COOH intermediates. This two‐step plastic‐to‐fuel conversion may help to simultaneously address the white pollution crisis and harvest highly valuable multicarbon fuels in natural environments.
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