Abstract

AbstractThe direct catalytic decomposition of NO with high activity and N2 selectivity is a great challenge at low temperature under excess oxygen. Herein, we report the NO decomposition by microwave catalysis over BaMeO3 (Me=Mn, Co, Fe) mixed oxides for the first time at low temperature under excess oxygen, for which the BaCoO3 catalyst has an outstanding activity with a high NO conversion and N2 selectivity up to 99.8 % and 99.9 %, respectively, even at 250 °C. Comparatively, the best NO conversion is 93.7 % for BaMnO3 and only 64.1 % for BaFeO3 under microwave irradiation. H2 temperature‐programmed reduction, O2 temperature‐programmed desorption, and the microwave‐absorbing properties of the mixed oxides were characterized to illustrate possible reasons that cause such clear differences in the catalytic performance. Importantly, the apparent activation energies for BaMnO3, BaCoO3, and BaFeO3 are as low as 33.4, 13.7, and 46.7 kJ mol−1, respectively, which suggests a significant microwave catalytic effect.

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