Temperature programmed reduction with NO (NO-TPR) is introduced as a characterization method, by monitoring the reduction of CuII to CuI in a mixture of NH3 and NO. Since the NO-TPR method is based on the oxidation and reduction half cycles of the NH3-SCR reaction, quantitative information about the amount of active Cu in Cu-CHA is obtained. Furthermore, information on the stability and reactivity of reaction intermediates in the NH3-SCR cycle is obtained as well. The reduction of the Cu is followed by monitoring the consumption of NO, after oxidation of the catalyst in O2 or a mixture of NO and O2 to form the CuII state. Two distinct states of the Cu are revealed. The first state, corresponding to the reduction of a Cu-oxide species, is reduced around 130 °C and is observed at low Cu content only. The second state corresponds to the reduction of a Cu-nitrate species around 200–230 °C. The low-temperature activity of Cu-chabazite catalysts with low Cu content show the same trend as the Cu-nitrate species observed in NO-TPR. The fraction of Cu-oxide in NO-TPR decreases with increasing Cu content, leading to a nonlinear dependence of the NH3-SCR activity on the Cu-content. At high Cu content, all Cu forms a stable Cu-nitrate species, and the NH3-SCR activity becomes proportional to the Cu content. This agrees well with the known behavior of Cu-CHA catalysts, indicating that NO-TPR seems to be a viable method for the characterization of Cu-CHA materials as NH3-SCR catalysts.

Temperature-programmed reduction with NO as a characterization of active Cu in Cu-CHA catalysts for NH3-SCR

Negri C.;Berlier G.;Bordiga S.;
2019-01-01

Abstract

Temperature programmed reduction with NO (NO-TPR) is introduced as a characterization method, by monitoring the reduction of CuII to CuI in a mixture of NH3 and NO. Since the NO-TPR method is based on the oxidation and reduction half cycles of the NH3-SCR reaction, quantitative information about the amount of active Cu in Cu-CHA is obtained. Furthermore, information on the stability and reactivity of reaction intermediates in the NH3-SCR cycle is obtained as well. The reduction of the Cu is followed by monitoring the consumption of NO, after oxidation of the catalyst in O2 or a mixture of NO and O2 to form the CuII state. Two distinct states of the Cu are revealed. The first state, corresponding to the reduction of a Cu-oxide species, is reduced around 130 °C and is observed at low Cu content only. The second state corresponds to the reduction of a Cu-nitrate species around 200–230 °C. The low-temperature activity of Cu-chabazite catalysts with low Cu content show the same trend as the Cu-nitrate species observed in NO-TPR. The fraction of Cu-oxide in NO-TPR decreases with increasing Cu content, leading to a nonlinear dependence of the NH3-SCR activity on the Cu-content. At high Cu content, all Cu forms a stable Cu-nitrate species, and the NH3-SCR activity becomes proportional to the Cu content. This agrees well with the known behavior of Cu-CHA catalysts, indicating that NO-TPR seems to be a viable method for the characterization of Cu-CHA materials as NH3-SCR catalysts.
2019
9
10
2608
2619
http://pubs.rsc.org/en/journals/journal/cy
Hammershoi P.S.; Negri C.; Berlier G.; Bordiga S.; Beato P.; Janssens T.V.W.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2318/1724986
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