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An IR-Spectroscopic Study of the State of Zirconium in Supported Zirconocene Catalysts Full article

Journal Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210
Output data Year: 2004, Volume: 45, Number: 4, Pages: 547-553 Pages count : 7 DOI: 10.1023/B:KICA.0000038083.22397.bf
Tags Polymerization; Spectroscopy; Ethylene; Physical Chemistry; Zirconium
Authors Panchenko V.N. 1 , Danilova I.G. 1 , Zakharov V.A. 1 , Paukshtis E.A. 1
Affiliations
1 Boreskov Institute of Catalysis, Siberian Division, Russian Academy of Sciences, Novosibirsk, 630090 Russia

Abstract: The surface compounds of zirconium in SiO2/MAO/Cp2ZrMe2 (I) and SiO2/Cp2ZrMe2 (II) catalysts were studied by the IR spectroscopy of adsorbed CO at 93-293 K. It was found that the bridging and terminal complexes of CO were formed on the surface of the catalysts at 93 K; the adsorption of CO was reversible. At 293 K, CO was irreversibly inserted into the Zr-Me bond with the formation of various acyl compounds of zirconium; these compounds were characterized by absorption bands in the region 1495-1750 cm-1 in the IR spectrum. These data suggested the heterogeneity of the surface composition of zirconocene catalysts Iand II. Catalyst I, which was active in ethylene polymerization, contained surface zirconium complexes that can be considered as the precursors of active centers for ethylene polymerization.
Cite: Panchenko V.N. , Danilova I.G. , Zakharov V.A. , Paukshtis E.A.
An IR-Spectroscopic Study of the State of Zirconium in Supported Zirconocene Catalysts
Kinetics and Catalysis. 2004. V.45. N4. P.547-553. DOI: 10.1023/B:KICA.0000038083.22397.bf WOS Scopus РИНЦ ANCAN OpenAlex
Original: Панченко В.Н. , Данилова И.Г. , Захаров В.А. , Паукштис Е.А.
Исследование состояния циркония в нанесенных цирконоценовых катализаторах методом ИК-спектроскопии
Кинетика и катализ. 2004. Т.45. №4. С.580-586. РИНЦ
Dates:
Submitted: Feb 4, 2003
Published print: Jul 1, 2004
Identifiers:
Web of science: WOS:000223776200013
Scopus: 2-s2.0-4444281028
Elibrary: 14189924
Chemical Abstracts: 2004:671520
Chemical Abstracts (print): 142:135003
OpenAlex: W2135489418
Citing:
DB Citing
Web of science 7
Scopus 6
Elibrary 7
OpenAlex 6
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