POISONING OF ACTIVE SITES ON ZIEGLER-NATTA CATALYST FOR PROPYLENE POLYMERIZATION
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POISONING OF ACTIVE SITES ON ZIEGLER-NATTA CATALYST FOR PROPYLENE POLYMERIZATION
POISONING OF ACTIVE SITES ON ZIEGLER-NATTA CATALYST FOR PROPYLENE POLYMERIZATION
高分子科学(英文版)2008年26卷第5期 页码:547-552
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纸质出版:2008-09-20
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Kitti Tangjituabun, Sang Yull Kim, Yuichi Hiraoka, 等. POISONING OF ACTIVE SITES ON ZIEGLER-NATTA CATALYST FOR PROPYLENE POLYMERIZATION[J]. 高分子科学(英文版), 2008,26(5):547-552.
Kitti Tangjituabun, Sang Yull Kim, Yuichi Hiraoka, et al. POISONING OF ACTIVE SITES ON ZIEGLER-NATTA CATALYST FOR PROPYLENE POLYMERIZATION[J]. 2008, 26(5): 547-552.
Kitti Tangjituabun, Sang Yull Kim, Yuichi Hiraoka, 等. POISONING OF ACTIVE SITES ON ZIEGLER-NATTA CATALYST FOR PROPYLENE POLYMERIZATION[J]. 高分子科学(英文版), 2008,26(5):547-552.DOI:
Kitti Tangjituabun, Sang Yull Kim, Yuichi Hiraoka, et al. POISONING OF ACTIVE SITES ON ZIEGLER-NATTA CATALYST FOR PROPYLENE POLYMERIZATION[J]. 2008, 26(5): 547-552.DOI:
POISONING OF ACTIVE SITES ON ZIEGLER-NATTA CATALYST FOR PROPYLENE POLYMERIZATION
The effects of poisoning materials on catalytic activity and isospecificity of the supported Ziegler-Natta catalyst were investigated. A minor amount of simple structure of Lewis base
i.e.
methanol
acetone
ethyl acetate
was introduced into the catalyst slurry for partial poisoning catalytic active centers. It was found that the variations in deactivation power were in the order of methanol acetone ethyl acetate. The kinetic investigation via stopped-flow polymerization showed that poisoning compounds caused a decrease in activity through the reduction of the number of active sites whereas no effect on the degree of isotacticity was observed.
Abstract
The effects of poisoning materials on catalytic activity and isospecificity of the supported Ziegler-Natta catalyst were investigated. A minor amount of simple structure of Lewis base
i.e.
methanol
acetone
ethyl acetate
was introduced into the catalyst slurry for partial poisoning catalytic active centers. It was found that the variations in deactivation power were in the order of methanol acetone ethyl acetate. The kinetic investigation via stopped-flow polymerization showed that poisoning compounds caused a decrease in activity through the reduction of the number of active sites whereas no effect on the degree of isotacticity was observed.
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