MgCl2·6CH3OH: A Simple Molecular Adduct and Its Influence As a Porous Support for Olefin Polymerization

Gnanakumar, Edwin S. ; Gowda, Ravikumar R. ; Kunjir, Shrikant ; Ajithkumar, T. G. ; Rajamohanan, P. R. ; Chakraborty, Debashis ; Gopinath, Chinnakonda S. (2013) MgCl2·6CH3OH: A Simple Molecular Adduct and Its Influence As a Porous Support for Olefin Polymerization ACS Catalysis, 3 (3). pp. 303-311. ISSN 2155-5435

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Official URL: http://doi.org/10.1021/cs300730j

Related URL: http://dx.doi.org/10.1021/cs300730j

Abstract

A single phase molecular adduct, MgCl2·6CH3OH has been synthesized using MgCl2 and the simplest alcohol, methanol. Structural, spectroscopic, and morphological studies have been carried out for a better understanding of the single phase MgCl2·6CH3OH adduct. 13C CPMAS solid state NMR studies show all six methanol molecules are magnetically equivalent and present in a single environment around the Mg2+ center. Raman spectral analysis of the characteristic peak at 708 cm–1 substantiates octahedral coordination of six CH3OH molecules around Mg2+. Solid state 13C NMR measurements, made after heat treatment at different temperatures, have been utilized to understand the variations in CH3OH stoichiometry and coordination around Mg2+ with temperature. A titanated active catalyst, TiCl4 on MgCl2·6CH3OH, has also been synthesized and subjected to detailed characterizations. The active catalyst shows high surface area (102 m2/g) and mesoporosity. The titanated catalyst has been screened for ethylene polymerization reactions using different cocatalysts (R3Al; R= −CH3, −CH2CH3, and −CH2CH(CH3)2). A total of 7.25 kg of polyethylene per gram of catalyst has been obtained with Me3Al cocatalyst, which is six times higher in activity compared with commercial Me3Al/TiCl4/ MgCl2·6EtOH-supported catalyst. Although porosity influences the catalytic activity, other factors also seem to contribute to the total catalytic activity.

Item Type:Article
Source:Copyright of this article belongs to American Chemical Society.
ID Code:130193
Deposited On:05 Dec 2022 06:15
Last Modified:05 Dec 2022 06:15

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