Journal
POLYMER SCIENCE SERIES A
Volume 50, Issue 11, Pages 1101-1121Publisher
MAIK NAUKA/INTERPERIODICA/SPRINGER
DOI: 10.1134/S0965545X08110023
Keywords
-
Categories
Ask authors/readers for more resources
The article discusses recent results of kinetic analysis of propylene and ethylene polymerization reactions with several types of Ti-based catalysts. All these catalysts, after activation with organoaluminum cocatalysts, contain from two to four types of highly isospecific centers (which produce the bulk of the crystalline fraction of polypropylene) as well as several centers of reduced isospecificity. The following subjects are discussed: the distribution of active centers with respect to isospecificity, the effect of hydrogen on polymerization rates of propylene and ethylene, and similarities and differences between active centers in propylene and ethylene polymerization reactions over the same catalysts. Ti-based catalysts contain two families of active centers. The centers of the first family are capable of polymerizing and copolymerizing all alpha-olefins and ethylene. The centers of the second family efficiently polymerize only ethylene. Differences in the kinetic effects of hydrogen and alpha-olefins on polymerization reactions of ethylene and propylene can be rationalized using a single assumption that active centers with alkyl groups containing methyl groups in the beta-position with respect to the Ti atom, Ti-CH(CH3)R, are unusually unreactive in olefin insertion reactions. In the case of ethylene polymerization reactions, such an alkyl group is the ethyl group (in the Ti-C2H5 moiety) and, in the case of propylene polymerization reactions, it is predominantly the isopropyl group in the Ti-CH(CH3)(2) moiety.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available