原子转移自由基聚合
高分子化学
离子液体
共聚物
分散性
甲基丙烯酸甲酯
聚合
纤维素
化学
链式转移
聚合物
自由基聚合
材料科学
催化作用
有机化学
作者
Chunxiang Lin,Zhan Huai-yu,Minghua Liu,FU Shi-yu,Jiajun Zhang
标识
DOI:10.1016/j.carbpol.2009.04.032
摘要
Cellulose graft poly(methyl methacrylate) copolymers were prepared by atom transfer radical polymerization (ATRP) in an ionic liquid. Cellulose chloroacetate, as a macroinitiator, was first synthesized by direct acylation of cellulose with chloroacetyl chloride without any catalysts under mild conditions in an ionic liquid, 1-allyl-3-methylimidazolium chloride (BMIMCl). Then, the macroinitiator was used for the ATRP of MMA mediated by the CuBr and 2,2′-bipyridine (bpy) catalysis system. The copolymerization was carried out in BMIMCl without homopolymer byproduct. The polymers were easily separated from the catalyst when the ionic liquid was used as reaction medium. The grafting copolymers were characterized by means of 1H NMR, AFM and GPC. The results showed that the obtained copolymers had grafted polymer chains with well-controlled molecular weight and polydispersity, and the polymerization was a “living/controlled” system. Further, through AFM observation, it was found that the cellulose graft copolymer in solution could aggregate and self-assembly into sphere-like polymeric structure.
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