Preparation and characterization of long chain branched polypropylene mediated by different heteroaromatic ring derivatives

被引:20
作者
Wan, Dong [1 ,2 ]
Ma, Li [1 ]
Xing, Haiping [1 ,2 ]
Wang, Lu [1 ,2 ]
Zhang, Zhenjiang [1 ,2 ]
Qiu, Jian [1 ]
Zhang, Guangchun [1 ,2 ]
Tang, Tao [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Changchun 130022, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
Long chain branch; Polypropylene; Melt mixing; ISOTACTIC POLYPROPYLENE; MOLECULAR-WEIGHT; CROSS-LINKING; RADICAL FUNCTIONALIZATION; REACTIVE EXTRUSION; ELECTRON-BEAM; DEGRADATION; RHEOLOGY; POLYETHYLENE; HEAT;
D O I
10.1016/j.polymer.2012.12.014
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Three different heteroaromatic ring derivatives (coagents) were used to adjust the melt radical reaction of polypropylene (PP). From the results of high temperature H-1 NMR and high-temperature size-exclusion chromatography (HT-SEC), all the coagents could quickly convert the tertiary PP macroradicals into resonance stabilized macroradicals and effectively restrain the beta-scission of PP macroradicals. Long chain branched structures, without significant bimodal distribution of molecular weight, could be introduced into coagents-functionalized PP samples. Effect of chemical structures of heteroaromatic rings and electron-attracting groups on the molecular structures and melt properties of modified PP samples was studied. The possible reactions of coagents-functionalized PP samples in different theoretical molar ratio of coagent to alkoxy radical were also proposed according to the results of H-1 NMR, torque curves, rheological measurements and HT-SEC coupled with laser light scattering detector. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:639 / 651
页数:13
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