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The study of the adsorption of 1,3-diethers on the MgCl2 surface Full article

Journal Journal of Molecular Catalysis A: Chemical
ISSN: 1381-1169
Output data Year: 2013, Volume: 368, Pages: 159-162 Pages count : DOI: 10.1016/j.molcata.2012.12.004
Tags Ziegler-Natta catalysts; 1,3-Diethers; MgCl2 surface; IR spectroscopy
Authors Potapov A. G. 1 , Politanskaya L. V. 2
Affiliations
1 (Данные Web of science) Russian Acad Sci, Boreskov Inst Catalysis, Siberian Branch, Novosibirsk 630090, Russia
2 (Данные Web of science) Russian Acad Sci, NN Vorozhtsov Novosibirsk Inst Organ Chem, Siberian Branch, Novosibirsk 630090, Russia

Abstract: The interaction of 1,3-diethers and MgCl2 support was studied. It was found 1,3-diethers interact with the surface of MgCl2 support more selectively than esters. 1,3-Diethers form several surface complexes of different strength. At that, a strength of all surface complexes of 1,3-diethers considerably exceeds a strength of surface complexes of ethyl benzoate. The strength of some surface complexes of 1,3-diethers is close to that of surface complexes of dibutyl phthalate, and dibutyl phthalate is able to substitute 1,3-diethers from these complexes. The least strong surface complexes of 1,3-diethers are labile and can also be removed from the MgCl2 surface without action of any electron donors. In contrast to the MgCl2 support, the catalyst contains only more strong and unremovable surface complexes of 1,3-diether. This testifies on the formation of certain faces of MgCl2 during catalyst preparation in the presence of 1,3-diether contrary to the formation of different MgCl2 faces at the preparation of the MgCl2 support. (C) 2012 Elsevier B.V. All rights reserved.
Cite: Potapov A.G. , Politanskaya L.V.
The study of the adsorption of 1,3-diethers on the MgCl2 surface
Journal of Molecular Catalysis A: Chemical. 2013. V.368. P.159-162. DOI: 10.1016/j.molcata.2012.12.004 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Mar 1, 2013
Identifiers:
Web of science: WOS:000315176600022
Scopus: 2-s2.0-84873596878
Elibrary: 20433095
OpenAlex: W2023021591
Citing:
DB Citing
Web of science 18
Scopus 17
Elibrary 17
OpenAlex 18
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