Oxidative dehydrogenation of ethane over vanadium-based hexagonal mesoporous silica catalysts

Abstract

Vanadium-containing hexagonal mesoporous silica catalysts were tested in oxidative dehydrogenation of ethane. V-HMS catalysts (0.3–9.0 wt.% V) were prepared by impregnation with solution of vanadyl acetylacetonate, and by incorporation of vanadium in the synthesis process. The prepared catalysts achieved a different distribution of vanadium species (isolated monomeric units with tetrahedral coordination, oligomeric units connected by V O V bonds up to distorted tetrahedral coordination, two-dimensional polymeric units in octahedral coordination, and bulk vanadium oxides). The contribution deals with the understanding of the relationship between the distribution of vanadium species and their activity in ODH of ethane. It has been found that both monomeric and oligomeric vanadium species play important role in ODH of ethane. The activity correlated with the population of oligomeric tetrahedrally coordinated vanadium species, which were evidenced by the UV–vis band at 315 nm. To analyze this effect, V-HMS catalysts were characterized by means of UV–vis spectroscopy, H 2-TPR and N 2-adsorption.