Small addition of potassium to V/Ti-oxide catalyst (K:V=0.19), consisting of 3.7 monolayer VOx , increased activity and selectivity in partial oxidation of toluene. In order to elucidate the nature of vanadia species formed on the surface of V/Ti-oxide upon potassium doping, the catalysts were studied by transient kinetics method. The transient product responses during toluene oxidation by the ...

The oxidative dehydrogenation (ODH) of propane to propylene by supported vanadia catalysts has received much attention in recent years, but different reactivity trends have been reported for this catalytic reaction system. In the present investigation, the origin of these differing trends are investigated with synthesis of supported V/SiO2, V/TiO2, and V/Al2O3 catalysts prepared with three diff...

The effect of the suppport on oxidative dehydrogenation activity for vanadia/ceria systems is examined for the oxidation of methanol to formaldehyde by use of well-defined VO(x)/CeO(2)(111) model catalysts. Temperature-programmed desorption at low vanadia loadings revealed reactivity at much lower temperature (370 K) as compared to pure ceria and vanadia on inert supports such as silica. Densit...

Supported transition metal oxides and vanadium-containing multi-metallic oxides were investigated to develop new catalysts for the catalytic destruction of highly toxic polychlorinated aromatic pollutants such as polychlorinated benzenes, polychlorinated dibenzo-p-dioxins (PCDDs), dibenzofurans (PCDFs), and/or biphenyls (PCBs) from waste gases. The decomposition of 1,2-dichlorobenzene (Cl2Bz) w...

The supported K2O–V2O5/Al2O3 catalytic system was designed to create surfaces that were 100% acidic, 100% basic, 100% redox, mixed redox-acidic and mixed redox-basic. The resulting nature of the surface sites was controlled by the impregnation of the specific additives (K-basic or V-redox/acidic), their order of impregnation and their surface coverage. The exact locations of the surface methoxy...

The structure of vanadia species supported on zirconia depends on VOx surface density and on the temperature of catalyst oxidation pretreatments. X-ray diffraction and Raman and UV-visible spectroscopies show that supported VOx species form polyvanadate domains of increasing size and ultimately monolayers and clusters as vanadium surface density increases. Initial propene selectivities in oxida...