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In relation to this article, we declare that there is no conflict of interest.
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Received August 18, 2003
Accepted December 1, 2003
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Recycling of Methylaluminoxane (MAO) Cocatalyst in Ethylene Polymerization with Supported Metallocene Catalyst

1LG Chemical Ltd./Research Park, Moonji-dong 104-1, Yuseong-ku, Daejeon 305-380, Korea 2Department of Molecular Science and Technology, Ajou University, Suwon 442-749, Korea 3Department of Chemistry, University of Illinois at Urbana-Champagne, Illinois 61801, Korea
jsoh@lgchem.co.kr
Korean Journal of Chemical Engineering, January 2004, 21(1), 110-115(6), 10.1007/BF02705387
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Abstract

The economy of the metallocene catalyst system in olefin polymerization depends more on the cost of methylaluminoxane (MAO) cocatalyst rather than on the catalyst cost since high ratio of cocatalyst to catalyst is required to have sufficient activity. The conditions to minimize the consumption of MAO have been studied for the ethylene polymerization with supported metallocene catalyst. By introducing the prepolymerization step, in which the supported metallocene catalyst is activated at high MAO concentration before polymerization, the MAO could be recovered after the prepolymerization and recycled repeatedly for the subsequent activation with marginal decrease in activity. No extra MAO was needed during the main polymerization. The addition of small amount of MAO or less expensive alkylaluminum at each recycle step kept the catalyst activity to the initial level. It compensates the MAO losses occurring both by the incomplete decantation of MAO solution and by the reaction with metallocene complex or impurities. As a result, the actual consumption ratio of Al/Zr in moles in commercial applications could be reduced to about 30 without sacrificing the activity. This value is significantly low considering that conventionally an Al/Zr ratio of 1,000 is required for sufficient activity.

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