Bimodal Ultrahigh Molecular Weight Polyethylenes Produced from Supported Catalysts: The Challenge of Using a Combined Catalyst System

被引:9
作者
Liu, Hao [1 ]
Bastiaansen, Cees W. M. [1 ,2 ]
Goossens, Johannes G. P. [3 ]
Schenning, Albertus P. H. J. [1 ]
Severn, John R. [1 ,4 ]
机构
[1] Eindhoven Univ Technol, Dept Chem Engn & Chem, Funct Organ Mat & Devices, NL-5600 MB Eindhoven, Netherlands
[2] Queen Mary Univ London, Sch Engn & Mat Sci, London E1 4NS, England
[3] Eindhoven Univ Technol, Dept Chem Engn & Chem, Lab Polymer Mat, NL-5600 MB Eindhoven, Netherlands
[4] DSM Ahead B V, NL-6160 MD Geleen, Netherlands
关键词
bimodal distribution; polyethylene; silica nanoparticle; single-site catalyst; SINGLE-SITE CATALYSTS; ETHYLENE POLYMERIZATION; METALLOCENE CATALYSTS; REACTOR BLENDS; ZIEGLER-NATTA; UHMWPE; DISTRIBUTIONS; IMMOBILIZATION; ACTIVATION; POLYMERS;
D O I
10.1002/macp.201600490
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Molecular precatalysts complexes (nBuCp)(2)ZrCl2 (Zr) and (eta 1:eta 5-Me2NCH2CH2C5Me4)CrCl2 (Cr) have been successfully supported on silica nanoparticles, via a single support (SS) or a double support (DS) strategy. These catalyst systems have been successfully used to produce bimodal polyethylenes with an ultrahigh molecular weight polyethylene content in a single reactor. The SS and DS catalyst systems have been fully evaluated under an identical polymerization condition to assess the challenges in tailoring the molecular weight distribution. The results show that a detrimental interaction exists between Zr and Cr catalysts, part of the Cr catalyst species is deactivated during polymerization in the both DS and SS systems. The detrimental interaction in the DS system is reduced because the catalysts are supported on separate nanoparticles. But, surprisingly the two catalysts in the DS system are still able to "communicate" to each other via cocatalyst-induced catalyst leaching or other potential reasons.
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页数:9
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