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Bimodal Ultrahigh Molecular Weight Polyethylenes Produced from Supported Catalysts: The Challenge of Using a Combined Catalyst System
Author(s) -
Liu Hao,
Bastiaansen Cees W. M.,
Goossens Johannes G. P.,
Schenning Albertus P. H. J.,
Severn John R.
Publication year - 2017
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.201600490
Subject(s) - catalysis , polymerization , polyethylene , leaching (pedology) , molar mass distribution , nanoparticle , chemical engineering , polymer chemistry , catalyst support , chemistry , materials science , polymer , nanotechnology , organic chemistry , engineering , environmental science , soil science , soil water
Molecular precatalysts complexes ( n BuCp) 2 ZrCl 2 (Zr) and (η1:η5‐Me 2 NCH 2 CH 2 C 5 Me 4 )CrCl 2 (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.