Citation:
Xiaoxia Dai, Weiyu Jiang, Wanglong Wang, Xiaole Weng, Yuan Shang, Yehui Xue, Zhongbiao Wu. Supercritical water syntheses of transition metal-doped CeO2nano-catalysts for selective catalytic reduction of NO by CO: An in situ diffuse reflectance Fourier transform infrared spectroscopy study[J]. Chinese Journal of Catalysis,
;2018, 39(4): 728-735.
doi:
10.1016/S1872-2067(17)63008-0
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In the present study, we synthesized CeO2 catalysts doped with various transition metals (M=Co, Fe, or Cu) using a supercritical water hydrothermal route, which led to the incorporation of the metal ions in the CeO2 lattice, forming solid solutions. The catalysts were then used for the selective catalytic reduction (SCR) of NO by CO. The Cu-doped catalyst exhibited the highest SCR activity; it had a T50 (i.e., 50% NO conversion) of only 83℃ and a T90 (i.e., 90% NO conversion) of 126℃. Such an activity was also higher than in many state-of-the-art catalysts. In situ diffuse reflectance Fourier transform infrared spectroscopy suggested that the MOx-CeO2 catalysts (M=Co and Fe) mainly followed an Eley-Rideal reaction mechanism for CO-SCR. In contrast, a Langmuir-Hinshelwood SCR reaction mechanism occurred in CuO-CeO2 owing to the presence of Cu+ species, which ensured effective adsorption of CO. This explains why CuO-CeO2 exhibited the highest activity with regard to the SCR of NO by CO.
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