Abstract
The essential roles of octahedrally coordinated cations (B-site in AB2O4 formula) in Co3-xCrxO4 spinel oxides in the total oxidation of propane were demonstrated, using a series of Co3-xCrxO4 spinel oxides with different Co/Cr molar ratios derived from layered double hydroxides. The catalytic activity was strongly related to the compositions of B-site cations. The Co2CrO4 catalyst with B-sites equally occupied with Co and Cr cations was more active than the Co3O4 (Co cations only in B-sites) and CoCr2O4 (Cr cations only in B-sites), giving turnover frequencies of 0.86 × 10-3, 0.72 × 10-3 and 0.11 × 10-3 s−1 at 250 °C (under kinetically-controlled reaction), respectively. Kinetics and density functional theory (DFT) calculations on the Co2CrO4 and CoCr2O4 catalysts indicated that the reaction followed a Langmuir-Hinshelwood mechanism, and the adsorption of oxygen on the former was easier. Moreover, the cleavage of the first C–H bond in the propane as the rate-determining step was more favored on the Co2CrO4, which accounted for its higher activity. These findings thus provide valuable insights on the mechanistic roles of B-site cations of spinel oxides in total oxidation of hydrocarbon.
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