Abstract
Magnesia-supported palladium catalysts were prepared from chemical vapour deposition (CVD) of [Pd(C3H5)(C5H5)] and incipient wetness impregnation of [Pd(C3H5)Cl]2 and [Pd(acac)2]. DRIFT spectroscopy of adsorbed CO on prereduced catalysts indicates that the electronic state of metal particles depends on the preparation methodology and markedly on the organometallic precursor. Inn-heptane reforming at 500°C, the highest activity and selectivity were shown by the CVD-based system. Chloride ions deriving from the impregnation solvent exchange with surface hydroxyls. Acidic Mg-Cl sites are thus formed, which induce a beneficial effect on the catalytic properties. The reforming activity collapsed when a chlorine-containing precursor was used, due to a partial coverage of the palladium surface with chemisorbed chlorine atoms.
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Kappers, M., Dossi, C., Psaro, R. et al. DRIFT study of CO chemisorption on organometallics-derived Pd/MgO catalysts: the effect of chlorine. Catal Lett 39, 183–189 (1996). https://doi.org/10.1007/BF00805581
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DOI: https://doi.org/10.1007/BF00805581