Role of potassium on the structure and activity of alumina-supported vanadium oxide catalysts for propane oxidative dehydrogenation

Abstract

The influence of potassium on the structure and properties of alumina-supported vanadium oxide catalysts has been studied by in situ Raman spectroscopy, temperature-programmed reduction (TPR), X-ray photoelectron spectroscopy (XPS), a probe reaction of acid/base–redox sites (methanol chemisorption) and tested in oxidative dehydrogenation (ODH) of propane. Potassium coordinates to surface vanadium oxide species altering its structure but does not form bulk compounds, possibly because the total V+K coverage does not reach the monolayer coverage on alumina. The interaction of K with V weakens the terminal VO bond. K-doped alumina (KAl)-supported vanadia catalysts show lower acidity, a decrease of reducibility and a decrease of propane conversion values. These trends do not correspond with the changes in the terminal VO bond energy. Thus, it appears that the terminal VO bond of surface vanadium oxide species is not the active site for propane ODH, oxidation of methanol to formaldehyde and for the reduction of surface vanadium oxide species by hydrogen. Potassium also changes the acid–base characteristic of the system and decreases the acidic character of surface vanadia. This shift in the acid–base character to a more basic system must also account for the better selectivity in propane ODH due to a variation in the interaction between the intermediates and the surface.