Journal of Catalysis, Vol.331, 138-146, 2015
On the metal-support synergy for selective gas-phase ethanol oxidation over MgCuCr2O4 supported metal nanoparticle catalysts
Achieving high yields in the production of bulk chemicals is an important goal for the chemical industry. We investigated the influence of the metal on the catalytic performance of M/MgCuCr2O4 (M = Cu, Ag, Pd, Pt, Au) catalysts to better understand the metal-support synergy for the aerobic oxidation of ethanol. Pt/MgCuCr2O4 and Pd/MgCuCr2O4 are more active and less selective for ethanol oxidation than the other catalysts, mainly because they can dehydrogenate and then cleave the carbon-carbon bonds in ethanol at relatively low temperature. Because of the facile oxidation of Cu-0 and Ag-0 under aerobic oxidation conditions, Cu/MgCuCr2O4 and Ag/MgCuCr2O4 are less active for ethanol oxidation. On contrary, Au/MgCuCr2O4 is a very active, selective and stable,catalyst for sustainable production of acetaldehyde, achieving 96% selectivity at full ethanol conversion (space-time-yield up to 583 g(aldehyde) g(Au)(-1)h(-1)) at 250 degrees C. Low gold loading and high gold dispersion are important to enhance the Au-0-Cu+ synergy and the catalytic efficiency of Au/MgCuCr2O4. (C) 2015 Elsevier Inc. All rights reserved.