Search results for "temperature-programmed reduction"
showing 3 items of 13 documents
Effect of Pre-Reduction on the Properties and the Catalytic Activity of Pd/Carbon Catalysts: A Comparison with Pd/Al2O3
2013
The effect of pre-reduction in solution with chemical reagents on the catalytic performance and catalyst properties of Pd/carbon catalysts was systematically investigated with a multitechnique approach. The results are critically discussed in comparison to those recently obtained on analogous Pd/alumina catalysts. It was proved that the Pd phase on the carbon surface is characterized by a high mobility, opposite to what occurs on alumina. As a result, the Pd particles on carbon aggregate together during pre-reduction, with a consequent decrease in available metal surface. Pd particles remain aggregated also in reaction conditions; the decreased Pd dispersion negatively affects the catalyst …
Direct synthesis of methyl isobutyl ketone in gas-phase reaction over palladium-loaded hydroxyapatite
2005
Several compositions of palladium-loaded calcium hydroxyapatite Pd(x)/CaHAp were prepared and characterized by XRD, IR, and UV–visible spectroscopy and temperature-programmed reduction (TPR). The acid–base properties of the samples were studied with the use of butan-2-ol conversion and IR spectroscopy coupled with lutidine adsorption/desorption. Calcium hydroxyapatite bears Lewis acid sites of moderate strength and a limited number of Bronsted acid sites, which produce butenes by dehydration. The selectivity of the dehydrogenation reaction (formation of methyl ethyl ketone) is very limited in the absence of oxygen but indicates the existence on the surface of phosphate of basic sites that a…
Total oxidation of VOCs on Au nanoparticles anchored on Co doped mesoporous UVM-7 silica
2012
Abstract Gold deposited on a cobalt containing siliceous mesoporous structure, UVM-7, presents a good catalytic performance in the total oxidation of propane and toluene. The presence of both gold and cobalt is necessary as bimetallic Au/Co-UVM-7 catalysts are remarkably more active than monometallic Au/UVM-7 or Co-UVM-7 catalysts. The improved activity of the bimetallic AuCo-samples if compared to gold free cobalt catalysts can be explained on the basis of the enhanced reducibility of some cobalt species in the presence of gold, which facilitates the redox cycle. This high reducibility of cobalt species in the bimetallic samples is probably due to the formation of Co 3 O 4 domains at the g…