Abstract

The selective oxidation of propane to acrylic acid on MoVTeNbO x catalysts with varying concentrations of vanadium, tellurium and niobium was investigated. Catalysts containing M1 phase were obtained over the compositional range of MoV 0.14–0.22Te 0.1–0.2Nb 0.1–0.2O x . Vanadium containing sites in the M1 phase are drastically more active for propane activation than in other materials studied. The catalytic activity is directly correlated to its fraction in the overall material and in particular the M1 phase. High concentrations of tellurium induce the formation of the M2 phase decreasing so the overall activity of the catalysts. The intrinsic activity of the M1 phase is, however, independent of the tellurium concentration. Although the presence of the M1 phase is not a stringent requirement for the oxidative dehydrogenation of propane to propene, it is required to oxidize the intermediately formed propene with high selectivity to acrylic acid. The active sites for propane activation and propene oxidation are structurally coupled, because the ratio between the rates of the two reactions was always 1:25. Oxygen defect sites in mixed oxides seem to enhance interaction with acrylic acid and lead to decarboxylation and total oxidation.

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