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  • 1
    ISSN: 1572-879X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Different magnesium vanadate phases, V-Mg-O phases (α- Mg2V2O7, Mg3V2O8 and β- MgV2O6), MgO and V2O5 oxides have been compared with respect to their surface properties and their oxygen exchange capacities with C18O2 in the gas phase. By temperature- programmed desorption of carbon dioxide, the absence of any basic impurities (i.e., MgO or residual oxidised K impurities resulting from the preparation) has been evidenced on the surface of magnesium vanadate phases. This demonstrates that the catalytic properties of the magnesium vanadate phases for oxidative dehydrogenation of propane as previously studied cannot be explained by synergetic effects due to the presence of any basic component impurities since they are absent in this case. While on MgO an important surface exchange process occurs with C18O2 of the gas phase, this exchange is very low on V2O5 and pure V-Mg-O phases. A comparison of the different magnesium vanadate phases in the same experimental conditions indicates that the α-Mg2V2O7 phase (which exhibited the highest selectivity for oxidative dehydrogenation of propane to propene) shows the lowest lattice oxygen exchange with C18O2 of the gas phase. This is another specificity of this phase.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1572-879X
    Keywords: dry reforming of methane ; temporal analysis of products (TAP) ; isotopic transient kinetic experiments ; bifunctional mechanism ; MgO-promoted ruthenium catalysts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The addition of MgO to a ruthenium catalyst dispersed on an inert activated carbon is found to improve the catalyst selectivity and stability in the dry reforming of methane to syngas. Steady-state and isotopic transient kinetic experiments carried out in a TAP reactor have revealed a cooperative interaction between the metal and the basic oxide in the CO2/CH4 reaction via a bifunctional mechanism. This specific effect is proposed to explain the discovered promoting effect.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1572-879X
    Keywords: rhodium ; rhodium-alumina ; active phase-support interaction ; hydrogenation of crotonaldehyde ; temperature-programmed reduction ; XANES
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The effects of the rhodium (oxidation) state on the activity and selectivity for the crotonaldehyde hydrogenation reaction over Rh/Al2O3 and Rh/SiO2 catalysts were examined using the techniques of temperature-programmed reduction, hydrogen chemisorption and X-ray absorption near-edge structure (XANES). In the alumina-supported system, the active phase-support interaction is shown to affect the chemical behavior of rhodium under the influence of a reductive atmosphere by stabilizing Rh3+ species. This behavior is not observed (as expected) for Rh/SiO2 catalysts. The structural and electronic bases of the active phase-support interaction and the effect of the latter phenomenon on the hydrogenation of crotonaldehyde are discussed.
    Type of Medium: Electronic Resource
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