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
高分子化学
工程类
作者
Xingchen Jiao,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
Reported here is the first highly selective conversion of various waste plastics into C2 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 CH3 COOH without using sacrificial agents. As an example, polyethylene is photodegraded 100 % into CO2 within 40 h by single-unit-cell thick Nb2 O5 layers, while the produced CO2 is further photoreduced to CH3 COOH. Various methods and experiments disclose that O2 and . OH radicals trigger the oxidative C-C cleavage of polyethylene to form CO2 , while other investigations show that the yielded CH3 COOH stems from CO2 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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