Catalysis of Ethylene to Linear Low-Density Polyethylene with Iron-Based Diimine Complex Immobilized on Calcosilicate and Silica-Supported rac-Et(Ind)2ZrCl2

被引:4
|
作者
Yan, Feng-Wen [1 ]
Xu, Hao [1 ]
Guo, Cun-Yue [1 ]
Zhang, Ming-Ge [1 ]
Zhang, Xiao-Hui [1 ]
Yang, Hai-Jian [2 ]
Yuan, Guo-Qing [1 ]
机构
[1] Chinese Acad Sci, Inst Chem, New Mat Lab, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
[2] S Cent Univ Nationalities, Coll Chem & Mat Sci, Key Lab Catalysis & Mat Sci Hubei Prov, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
catalysis; ethylene; LLDPE; calcosilicate; silica; IN-SITU COPOLYMERIZATION; DUAL-FUNCTIONAL CATALYSIS; STAR-LIKE POLYSTYRENES; BRANCHED POLYETHYLENE; ORGANIC SUPPORTS; POLYMERIZATION; METALLOCENE; SYSTEM; LLDPE; NANOCOMPOSITES;
D O I
10.1002/app.29903
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Iron-based diimine complex was immobilized on calcosilicate (CAS-1) to form heterogeneous precatalyst, which oligomerized ethylene to alpha-olefins even without the use Of aluminum alkyl Compounds as activators. The alpha-olefins, upon the catalysis of another catalyst, i.e., silica-supported rac-Et(lnd)(2)ZrCl2 copolymerized with ethylene to produce linear low-density polyethylene (LLDPE). The copolymerization reactions could be performed with the addition of triethylaluminum alone because of the introduction of methylaluminoxane to CAS-1 and silica during the supporting process. In addition to the formation of more alpha-olefins with lower molar mass, the layered structure of CAS-1 acted well in the controlled release of alpha-olefins in the copolymerization process. The simultaneous employment of the aforementioned two catalysts hence resulted in high catalytic activities, smooth kinetic process, well-regulated branching degree, higher molecular weights (M-n), improved thermal stability, and better morphology of the LLDPE obtained. (C) 2009 Wiley Periodicals, Inc. J Appl Polym Sci 112: 2298-2304, 2009
引用
收藏
页码:2298 / 2304
页数:7
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