Observation of Different Catalytic Activity of Various 1-Olefins during Ethylene1-Olefin Copolymerization with Homogeneous Metallocene Catalysts 英文参考文献.docVIP
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Observation of Different Catalytic Activity of Various 1-Olefins during Ethylene1-Olefin Copolymerization with Homogeneous Metallocene Catalysts 英文参考文献
Molecules 2011, 16, 373-383; doi:10.3390/moleculeOPEN ACCESS
molecules
ISSN 1420-3049
/journal/molecules
Article
Observation of Different Catalytic Activity of Various 1-Olefins
during Ethylene/1-Olefin Copolymerization with Homogeneous
Metallocene Catalysts
Mingkwan Wannaborworn, Piyasan Praserthdam and Bunjerd Jongsomjit *
Center of Excellence on Catalysis and Catalytic Reaction Engineering, Department of Chemical
Engineering, Faculty of Engineering, Chulalongkorn University, Bangkok 10330, Thailand
* Author to whom correspondence should be addressed; E-Mail: bunjerd.j@chula.ac.th;
Tel.: +66 2 2186869; Fax: +66 2 2186877.
Received: 18 November 2010; in revised form: 28 December 2010 / Accepted: 5 January 2011 /
Published: 7 January 2011
Abstract: This research aimed to investigate the copolymerization of ethylene and various
1-olefins. The comonomer lengths were varied from 1-hexene (1-C6) up to 1-octadecene (1-
C18) in order to study the effect of comonomer chain length on the activity and properties of
the polymer in the metallocene/MAO catalyst system. The results indicated that two
distinct cases can be described for the effect of 1-olefin chain length on the activity.
Considering the short chain length comonomers, such as 1-hexene, 1-octene and 1-decene,
it is obvious that the polymerization activity decreased when the length of comonomer was
higher, which is probably due to increased steric hindrance at the catalytic center hindering
the insertion of ethylene monomer to the active sites, hence, the polymerization rate
decreased. On the contrary, for the longer chain 1-olefins, namely 1-dodecene, 1-
tetradecene and 1-octadecene, an increase in the comonomer chain length resulted in better
activity due to the opening of the gap aperture between Cp(centroid)-M-Cp-(centroid),
which forced the coordination site to open more. This effect facilitated the polymerization
of the e
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