Effect of preparation procedure and composition of catalysts based on Mn and Ce oxides in the simultaneous removal of NOX and o-DCB

[Display omitted] •Better catalytic performance of co-precipitation than impregnation catalysts.•NO and o-DCB conversion above 80 % are reached with high Mn content catalysts.•There is surface Mn-CeO2 interaction in impregnation catalysts, but without formation of a solid solution.•Low Ce content im...

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Veröffentlicht in:Molecular catalysis 2020-11, Vol.495, p.111152, Article 111152
Hauptverfasser: Martín-Martín, J.A., Sánchez-Robles, J., González-Marcos, M.P., Aranzabal, A., González-Velasco, J.R.
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Sprache:eng
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Zusammenfassung:[Display omitted] •Better catalytic performance of co-precipitation than impregnation catalysts.•NO and o-DCB conversion above 80 % are reached with high Mn content catalysts.•There is surface Mn-CeO2 interaction in impregnation catalysts, but without formation of a solid solution.•Low Ce content improves physicochemical properties and catalytic performance.•CO2 selectivity above 80 % was obtained with all MnOX-CeO2 co-precipitation catalysts. Two series of catalysts based on Mn and Ce oxides were prepared by co-precipitation and impregnation, in order to study their physicochemical properties and catalytic performance in the simultaneous reduction of NO and oxidation of o-DCB. Co-precipitation catalysts showed better activity than those prepared by impregnation because of the formation of a MnOX-CeO2 solid solution, which improves redox and acid properties. Moreover, the catalysts with MnOX content between 80 and 90 mol.%, in which a coexistence between solid solution phase and Mn2O3 crystal was found, presented NO conversion above 90 % at temperatures below 250 °C and o-DCB conversion above 80 % at temperatures above 200 °C. The main by-products of SCR were N2O, produced in the whole range of temperature, and NO2, formed at temperatures above 300 °C. Selectivity to CO2 above 80 % was obtained using co-precipitation catalysts in all temperature range. Deactivation experiments showed that oxidation reaction strongly contributes to deactivate impregnation catalysts, whereas the effect of deactivation is lower in co-precipitation catalysts at high Mn contents.
ISSN:2468-8231
2468-8231
DOI:10.1016/j.mcat.2020.111152