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作 者:Chaoqun Wang Jian Xia Yuxing Zhang Xiaoqiang Hu Zhongbao Jian
机构地区:[1]State Key Laboratory of Polymer Physics and Chemistry,Changchun Institute of Applied Chemistry,Chinese Academy of Sciences,Changchun 130022,China [2]School of Applied Chemistry and Engineering,University of Science and Technology of China,Hefei230026,China
出 处:《National Science Review》2023年第7期119-128,共10页国家科学评论(英文版)
基 金:supported by the National Natural Science Foundation of China(22122110 and 21871250);the Jilin Provincial Science and Technology Department Program(20230101347JC)。
摘 要:The degradation of plastics has attracted much attention from the global community.Polyethylenes(PEs),as the most abundant synthetic plastics,are most frequently studied.PE is non-degradable and non-polar because of the sole presence of the pure hydrocarbon components.Concurrent incorporation of both in-chain cleavable and functional groups into the PE chain is an effective pathway to overcome the non-degradable and non-polar issue;however,the method for achieving this pathway remains elusive.Here,we report a strictly non-alternating(>99%)terpolymerization of ethylene with CO and fundamental polar monomers via a coordination-insertion mechanism using late transition metal catalysts,which effectively prevents the formation of undesired chelates originating from both co-monomers under a low CO concentration.High-molecular-weight linear PEs with both in-chain isolated keto(>99%)and main-chain functional groups are prepared.The incorporation of key low-content isolated keto groups makes PEs photodegradable while retaining their desirable bulk material properties,and the introduction of polar functional groups considerably improves their surface properties.
关 键 词:degradable plastic homogeneous catalysis C1 chemistry non-alternating copolymerization POLYOLEFIN
分 类 号:TQ325.12[化学工程—合成树脂塑料工业]
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