Ethylene Polymerization by Phenyl Sulfide Bridged Dinuclear Zirconocene Complex/MAO

Yu Jing Nie; Ming Yang

doi:10.4028/www.scientific.net/AMR.181-182.809

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HomeAdvanced Materials ResearchAdvanced Materials Research Vols. 181-182Ethylene Polymerization by Phenyl Sulfide Bridged...

Ethylene Polymerization by Phenyl Sulfide Bridged Dinuclear Zirconocene Complex/MAO

Abstract:

The phenyl sulfide bridged Zirconocene complex [(C5H5)Cl2ZrC5H4CH2(C6H4-p)]2S has been synthesized by treating the dilithium salts of the phenyl sulfide bridged cyclopentadienyl ligand with two equivalents of C5H5ZrCl3(DME) and characterized by 1HMNR and elemental analysis. Homogenous ethylene polymerization by this complex has been conducted systematically in the presence of methylaluminoxane (MAO). The influence of the molar ratio [MAO]/[Cat], the catalyst concentration, time and temperature have been studied in detail. The highest catalytic activity of 1 is up to 13.78×105 g PE/mol•Cat•h. Higher temperature is favorable for increasing the catalytic activity for 1. High temperature gel permeation chromatography (HT-GPC) proves the production of polyethylene with a broad molecular weight distribution (MWD), which is reached 6.02.

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Advanced Materials Research (Volumes 181-182)

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809-813

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https://doi.org/10.4028/www.scientific.net/AMR.181-182.809

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Online since:

January 2011

Authors:

Yu Jing Nie, Ming Yang

Keywords:

Binuclear, Polyethylene (PE), Polymerization, Zirconocene Catalyst

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