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Design of novel malonates as internal donors for MgCl2-supported TiCl4 type polypropylene catalysts and their mechanistic aspects, Part 1

✍ Scribed by Shohjiroh Tanase; Kiyokazu Katayama; Nobuhiro Yabunouchi; Takanori Sadashima; Norio Tomotsu; Nobuhide Ishihara


Book ID
104057242
Publisher
Elsevier Science
Year
2007
Tongue
English
Weight
661 KB
Volume
273
Category
Article
ISSN
1381-1169

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✦ Synopsis


Various new malonate compounds (R 1 R 2 C(COOBu) 2 ) with different substituents (R 1 , R 2 ) were systematically synthesized and investigated for use as an internal donor (ID) in combination with a MgCl 2 -supported TiCl 4 type catalyst, a triethylaluminum (TEA) co-catalyst and an alkoxysilane external donor (ED) for application in propylene polymerization. The catalytic activity and isotacticity of polypropylene (PP) greatly depended on not only the oxygen electron density of the ED, but also on the molecular volume of the ID. Furthermore, the mechanism of the active site formation was discussed with respect to the composition of the catalyst treated with TEA and ED, and with respect to the temperature rising elution fractionation (TREF) results of PP and so on. It was presumed that the desorption of malonates near Ti species from MgCl 2 caused the generation of atactic PP sites, and the decrease of the isotacticity of PP.