H. Idriss, C. Diagne, J. Hindermann
Sep 1, 1995
Citations
3
Influential Citations
216
Citations
Quality indicators
Journal
Journal of Catalysis
Abstract
Abstract The reactions of acetaldehyde were investigated on the surfaces of CeO 2 , 3 wt% Pd/CeO2, 3 wt% Co/CeO 2 , and 3 wt% Pd-3 wt% Co/CeO 2 by temperature programmed desorption (TPD) and infrared spectroscopy (FT-IR). The surface and bulk compositions of these catalysts were studied by X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and CO chemisorption. XRD patterns indicated that the fluorite structure of CeO 2 was maintained in all catalysts (calcined and H 2 -reduced) and that there were no apprediable differences in particle dimension between CeO 2 alone (96 A) and metal/CeO 2 catalysts (84-98 A). Reduced catalysts were investigated by XPS: Ce (3 d ) spectra indicated the precence of Ce 3+ cations, evidenced by V′ and U′ peaks at 885.0 and 903.7 eV, together with Ce 4+ species. Co 2 p spectra indicated the presence of Co 2+ cations, evidenced by the Co 2 p 3/2 line at 781.0 eV (and its satellite at about 788 eV) and Co 2 p 1/2 at 797.0 eV (and its satellite at about 804 eV). Pd metal was detected on Pd/CeO 2 and Pd-Co/CeO 2 . Several reactions of acetaldehyde were observed; they can be classified as oxidation, reduction, or carbon-carbon bond formation reactions. Oxidation to acetates and reduction to ethanol were observed on all catalysts; acetate species were identified by their IR bands at 1560-1540, 1451, 1400, 1343, and 1020 cm −1 at room temperature, and ethanol was observed to desorb at ca, 400 K during acetaldehyde TPD. Several other adsorbed species were observed (on hydrogen reduced catalysts) by IR: acetyl, fingerprinted by a 1684 cm −1 band on metal/CeO 2 , η 2 (C, O) acetaldehyde (bands at 1220-1268, 1175-1156, 950-940 cm −1 ) on Pd/CeO 2 and Pd-Co/CeO 2 , and CO adsorbed by its carbon to metal (Pd, Co) and by its oxygen to reduced Ce, giving rise to bands at 1730, 1739, and 1750 cm −1 . Four C-C bond formation reactions were observed: (1) β-aldolization to crotonaldehyde and crotyl alcohol (most prominent on CeO 2 alone), (2) acetate ketonization to acetone and CO 2 on CeO 2 and Co/CeO 2 , (3) acetyl reaction with methyl species to give acetone on Pd/CeO 2 , Co/CeO 2 , and Pd-Co/CeO 2 (this acetone desorption was coincident with propane desorption on Pd/CeO 2 and Co/CeO 2 ), (4) reductive coupling of two molecules of acetaldehyde to butene and butadiene (on CeO 2 and Co/CeO 2 ). Pd-Co/CeO 2 adsorbed four times more CO than did Pd/CeO 2 or Co/CeO 2 and was the most active for acetaldehyde conversion.