Abstract
The effect of substitution of cobalt by iron in perovskite-type oxides GdCoxFe1-xO3 (х = 0; 0.5 and 1) on their physical properties and catalytic performance in dry reforming of methane (DRM) was investigated. The perovskites were synthesized by sol-gel technology and characterized by XRD, DTG/TG, BET specific area, TPR and SEM. It was established that the introduction of cobalt into the B site of the perovskite-type structure of ferrite leads to an increase in catalytic performance, and, consequently, to a decrease in the process temperature. It was found that catalytic activity depends on the proportion of cobalt in the B site and increases in the row: GdFeO3 < GdCo0.5Fe0.5O3 < GdCoO3. Probably, such behavior of Co-containing catalysts is associated with the formation and stabilization of a more catalytically active Co–Gd2O3 system under the action of the reaction mixture. It has been assumed that the element in A-site (Gd) is responsible for dissociative chemisorption of CO2 and ions in site B (Fe and Co) are responsible for the formation of atomic hydrogen.
Published Version
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