Abstract
The effect of modification with metal salts and acids on the acid-base characteristics and the catalytic properties of active aluminum oxide in the reaction of methyl phenyl carbinol dehydration to styrene was studied using the IR spectroscopy of adsorbed base molecules. The surface treatment of γ-Al2O3 with chromium and nickel cations decreased the catalyst activity because of the occurrence of hydrogenation side reactions. The appearance of strong Bronsted and Lewis acid sites as a result of modification with sulfate, nitrate, and fluoride anions accelerated the deactivation of the catalyst. Upon modification with acetic acid solutions, additional Lewis acid sites with QCO = 33.5−34 kJ/mol were formed on the surface of aluminum oxide, and the concentration of strong basic sites with PA = 900 kJ/mol decreased; this facilitated an increase in the catalyst activity and a decrease in the rate of catalyst deactivation.
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