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ICAR ATRP OF ACRYLONITRILE UTILIZING A MODERATE TEMPERATURE RADICAL INITIATOR

ICAR ATRP OF ACRYLONITRILE UTILIZING A MODERATE TEMPERATURE RADICAL INITIATOR

作     者:Fei-jun Zhang 刘晓辉 

作者机构:School of Materials Science and EngineeringKey Lab of Hollow Fiber Membrane Material and Processes of Ministry of EducationTianjin Polytechnic University 

出 版 物:《Chinese Journal of Polymer Science》 (高分子科学(英文版))

年 卷 期:2013年第31卷第12期

页      面:1613-1622页

核心收录:

学科分类:081704[工学-应用化学] 07[理学] 08[工学] 0817[工学-化学工程与技术] 070305[理学-高分子化学与物理] 080501[工学-材料物理与化学] 0805[工学-材料科学与工程(可授工学、理学学位)] 0703[理学-化学] 

基  金:the National Natural Science Foundation of China(Nos.21074127 and 20804044) the Key Project of Chinese Ministry of Education(No.212003) 

主  题:Living polymerization ICAR ATRP Acrylonitrile Ambient temperature. 

摘      要:Initiators for continuous activator regeneration atom transfer radical polymerization (ICAR ATRP) of acrylonitrile was first conducted at various ambient temperatures (30-45 ℃). The key to success is ascribed to the usage of an appropriate low temperature radical initiator (2,2'-azobis(2,4-dimethylvaleronitrile)) and a high reactivity catalytic system (CuBr2/Me6TREN). The molar ratio of Cu catalyst tO AN as low as 1:20000 wa.s used to prepare well-defined polyacrylonitrile with controlled molecular weight and a narrow polydispersity index range of 1.08-1.30, while the monomer conversion was up to ca. 98%. The apparent activation energy of the polymerization was calculated to be 128.45 kJ/mol, suggesting that the polymerization strongly depended on reaction temperature. The very high chain-end functionality of the resultant polymer was confirmed by ^1H-NMR and GPC analyses as well as chain extension reaction.

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