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Catalytic oxidation of methane over hexaaluminates and hexaaluminate-supported Pd catalysts
Authors:Ben W. -L. Jang   R. M. Nelson   James J. Spivey   Meltem Ocal   R. Oukaci  George Marcelin
Affiliation:

a Center for Engineering and Environmental Technology, Research Triangle Institute, PO Box 12194, Research Triangle Park NC 27709-2194 USA

b Department of Chemical Engineering, University of Pittsburgh, 1249 Benedum Hall Pittsburgh, PA 15261 USA

Abstract:An aqueous (NH4)2CO3 coprecipitation method, based on that of Groppi et al. [Appl. Catal. A 104 (1993) 101–108] was used to synthesize Sr1−xLaxMnAl11O19− hexaaluminates. These materials were first synthesized by alkoxide hydrolysis. This synthesis route requires special handling of the starting materials and is not likely to be commercially practical. The materials prepared by (NH4)2CO3 coprecipitation have similar surface areas as those prepared by the alkoxide hydrolysis method. Their CH4 oxidation activity, measured as the temperature needed for 10% conversion of methane, is higher than those prepared by alkoxide hydrolysis. The La-substantiated material, LaMnAl11O19−, shows high surface area with 19.3 m2/g after calcination at 1400°C for 2 h. It is active for CH4 oxidation with T10% at 450°C using 1% CH4 in air and 70 000 cm3/h g space velocity. The stability and activity of LaMnAl11O19− prepared by (NH4)2CO3 coprecipitation method is a simple and important step forward for the application of CH4 catalytic combustion for gas turbines.
Keywords:Hexaaluminates   Catalytic combustion   Natural gas   Catalyst synthesis
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