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The surface chemistry of vanadium oxide catalysts

Thesis/Dissertation ·
OSTI ID:6761029

The surface chemistry of vanadium oxide catalysts was studied using UHV surface techniques and catalytic experiments at atmospheric pressure. In UHV, vanadium oxide films were grown on single crystal vanadium, Au(111), and Au foil substrates. Silica supported V{sub 2}O{sub 5} was used in the catalytic experiments. Auger electron spectroscopy and low energy electron spectroscopy revealed temperature dependent surface segregation of contaminants on the V(110) surface. Several cleaning procedures were used to remove persistent sulfur contamination. Vanadium oxide films grown on a Au(111) substrate were ordered. The growth mode and preparation of these films is discussed. The structure and Auger spectrum of the films were consistent with a V{sub 2}O{sub 3} surface. The TPD of hydrogen, ethanol, and ethylene were examined on this surface. The peak temperatures for the desorption of H{sub 2}O, CO, and CO{sub 2} were sensitive to the surface oxidation state. Polycrystalline V{sub 2}O{sub 5} supported on Au foil was also studied. Two water desorption peaks were observed after the adsorption of predissociated hydrogen. CO, CO{sub 2}, and C{sub 2}H{sub 4} were the principle desorption products after ethanol adsorption in UHV and at atmospheric pressure. The partial oxidation of methane and ethanol over V{sub 2}O{sub 5}-SiO{sub 2} was investigated. Methane oxidation with N{sub 2}O proceeded very slowly, however activation energies and rate laws were determined. Ethanol oxidation with O{sub 2} was more rapid. Catalyst dispersion were measured using irreversible oxygen uptake following reduction at 641 K. Ethanol partial oxidation was structure insensitive. The catalytic results were consistent with the UHV results from gold-supported samples.

Research Organization:
California Univ., Berkeley, CA (USA)
OSTI ID:
6761029
Country of Publication:
United States
Language:
English

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