4.7 Article

Simple anion-modified layered double oxides use for controlling Cu valence states for low-temperature CO-SCR

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SURFACES AND INTERFACES
卷 44, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.surfin.2023.103654

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Layered double oxides; Cu valence states regulation; NO elimination by CO; In-situ DRIFTS; Reaction mechanism

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This study focuses on the modification of transition metal catalysts for the selective catalytic reduction of NO by CO. It investigates the effect of different anions on the modification of CO-SCR catalysts. The results show that the use of nitrate ions as a regulator for LDH support leads to a high NO conversion rate, surpassing the use of sulfate ions. The study also highlights the importance of anion modulation in controlling the valence state of loaded copper species. In situ DRIFTS analysis reveals the reaction mechanisms at different temperatures. Overall, this work provides new insights for the valence modulation of copper and the modification of LDH materials in CO-SCR applications.
The modification of transition metal catalysts for selective catalytic reduction of NO by CO has been studied extensively. However, the effect of anion on CO-SCR catalyst modification is rarely reported. In this study, four different LDHs precursors were synthesized by using urea hydrothermal method and introducing different inorganic anions into the reaction system to control the self-assembly growth during the synthesis of LDHs. It is then loaded with a mass ratio of 7.5 % copper by impregnation method. The LDO(N)/Cu7.5 catalyst using nitrate ions regulated LDH as support achieved a high NO conversion of 96 % at 150 degrees C, which outdistanced the LDO(S)/ Cu7.5 with support regulated by sulfate ions. A series of characterizations demonstrated that CoFe-LDH modified with different anions could modulate the valence state of loaded copper species. Among them, the LDO(N)/Cu7.5 catalyst was able to produce more Cu+ as the active site for the catalytic reaction. In situ DRIFTS further revealed the reaction mechanism, following the E-R mechanism at <= 150 degrees C and the L-H mechanism at 200-350 degrees C. This work supplies a new idea for the valence modulation of copper and the modification of LDH materials for applications in CO-SCR.

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