氯化原位接枝反应制备羟基官能化CPE——结构表征  

PREPARATION OF HYDROXY-FUNCTIONALIZED CPE via in situ CHLORINATING GRAFT COPOLYMERIZATION——STRUCTURE CHARACTERIZATION

作　　者：朱雪真[1] 尹清明[1] 赵季若[1] 殷敬华[2] 冯莺[1] 王玉玲[1] 

机构地区：[1]青岛科技大学高分子科学与工程学院橡塑材料与工程教育部重点实验室,青岛266042 [2]中国科学院长春应用化学研究所高分子物理与化学国家重点实验室,长春130022

出　　处：《高分子学报》2007年第2期172-177,共6页Acta Polymerica Sinica

基　　金：国家自然科学基金重大基金(基金号50390090)资助项目;国家自然科学基金(基金号50373042)资助项目

摘　　要：以高密度聚乙烯(HDPE)为基体,采用气-固氯化原位接枝反应合成了以氯化聚乙烯(CPE)为骨架聚合物、丙烯酸-2羟基乙酯(HEA)为支链的接枝共聚物.反应中不需要加入任何引发剂,以氯自由基引发接枝及氯代反应,得到羟基官能化CPE接枝聚合物.并用1H-NMR,FT-IR,GPC及X-射线衍射等对接枝共聚物的结构进行了表征.A grafting copolymer （CPE-g-HEA） ,composed of poly（2-hydroxy ethyl acrylate） （PHEA） as branched chains and chlorinated polyethylene （CPE） as backbone, was synthesized by in situ chlorinating graft copolymerization. No any initiator was added in the system. The process of in situ chlorinating graft copolymerization comes from continuously introducing chlorine gas into the reaction mixtures composed of only high-density polyethylene powder and a little amount of 2-hydroxy ethyl acrylate （HEA） . When heated, a chlorine molecule decomposed into two chlorine radicals, which can lead to chlorination of PE, grafting of HEA to PE and homopolymerization of HEA as well.Tile structure of CPE-g-HEA was characterized by FT-IR, ^1 H-NMR, GPC and WAXD.The results of FT-IR, ^1H-NMR and GPC indicated the existence of grafting copolymer of CPE-g-HEA. It can be found that the side chains of the copolymer were very short compared with those of HEA by bulk polymerization according to the GPC trace, and also the copolymer had more branches compared with the aqueous suspension graft system （CPE-g-MMA） .

关 键 词：官能化 CPE—g—HEA 氯化原位接枝 结构表征 

分 类 号：O632.12[理学—高分子化学]