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Oxygen storage capacity of La1−xBO3 perovskites (with A′ = Sr, Ce; B = Co, Mn)—relation with catalytic activity in the CH4 oxidation reaction
Authors:S. Royer   H. Alamdari   D. Duprez  S. Kaliaguine
Affiliation:

aDepartment of Chemical Engineering, Laval University, Sainte Foy, Que., Canada G1K 7P4

bNanox Inc., 4975 rue Rideau, Local 100, Que., Canada G2E 5H5

cLACCO – UMR CNRS 6503, Université de Poitiers, F-86022 Poitiers Cedex, France

Abstract:The aim of this work was to study the effect of cation-substitution on the reducibility of the perovskite, as well as the effect on the catalytic activity for the CH4 oxidation reaction. Six perovskites (LaCoO3, LaMnO3, La1−xSrxMnO3 (x = 0.2, 0.4), and La1−xCexMnO3 (x = 0.05, 0.1)) were synthesized by reactive grinding. The reducibility of the perovskite was studied by means of the oxygen storage capacity (OSC) measurement. OSC was performed at different temperatures on LaCoO3 and LaMnO3, in order to elucidate the different mechanisms of reduction involved at each temperature. The substituted samples showed that reduction profile is modified at high-substitution degrees; however, no differences were observed on the OSC values (amount of most active oxygen, calculated after one pulse of CO) between the pure lanthanum sample and the substituted ones.

Tested in the CH4 oxidation reaction, the LaCoO3 sample was found to present a little higher activity than LaMnO3, even if the cobalt-based sample presented a smaller specific surface area. Moreover, all the substituted samples presented very slightly higher activities than the pure LaMnO3 solid. Because of the supposed redox oxidation mechanism (Mars-Van-Krevelen), this agrees well with the OSC results obtained for the reducibility of the manganese on these samples, by which it was observed that substitution does not clearly affect the immediate reduction of the manganese.

Keywords:Perovskite   OSC measurement   Catalytic activity in methane oxidation   Sr- and Ce-substitution effect
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