期刊
CHEMICAL ENGINEERING JOURNAL
卷 475, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2023.146005
关键词
Direct NO decomposition; Rh/PrO X; Deactivation; Rh active sites; Regeneration
This study investigates the application of Rh-supported metal oxides for direct nitrogen oxide decomposition (DND) and finds that the catalytic activity is deactivated over time due to oxygen poisoning, but can be regenerated through reductive treatments.
Direct nitrogen oxide decomposition (DND) is a promising alternative to the selective catalytic reduction (SCR) of nitrogen oxides for emissions control, as it eliminates the need to inject reductants such as urea/ammonia. The present study investigates the implementation of Rh-supported metal oxides for the DND reaction. Rh supported on each of PrOX, TiO2, Al2O3, and CeO2 were characterized, and we found that initially the catalytic activity on Rh/PrOX and Rh/TiO2 was very high, though it deactivated over time due to strong poisoning by adsorbed oxygen. This deactivation by oxygen poisoning was verified through in-situ DRIFTS, XPS, NEXAFS, O2-TPD measurements and density functional theory (DFT) calculations, respectively. This catalytic deactivation was positively regenerated by reductive treatments with CO or H2. This study discovers the mechanism of DND deactivation and regeneration over Rh-supported metal oxides, which will provide significant insight into further development of DND.
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