Active manganese oxide on MnOx-CeO2 catalysts for low-temperature NO oxidation:Characterization and kinetics study
来源期刊:Journal of Rare Earths2018年第2期
论文作者:Lingkun Meng Jun Wang Zhihui Sun Jinxin Zhu Hang Li Jianqiang Wang Meiqing Shen
文章页码:142 - 147
摘 要:MnOx-CeO2 catalysts were synthesized to investigate the active sites for NO oxidation by varying the calcination temperature. XRD and TEM results showed that cubic CeO2 and amorphous MnOx existed in MnOx-CeO2 catalysts. High temperature calcination caused the sintering of amorphous MnOx and transforming to bulk crystalline Mn2O3, H2-TPR and XPS results suggested the valence of Mn in MnOx-CeO2 was higher than pure MnOx, and decreased with the increasing calcination temperature, The turnover frequency(TOF) was calculated based on the initial reducibility according to H2-TPR quantitation and kinetic study. The TOF results indicated that the initial reducibility of amorphous MnOx with high valence manganese ions was equivalent to the active sites for NO oxidation. It can be inferred that the amorphous MnOx plays a key role in low-temperature NO oxidation.
Lingkun Meng1,Jun Wang1,Zhihui Sun1,Jinxin Zhu1,Hang Li1,Jianqiang Wang1,Meiqing Shen1,2,3
1. Key Laboratory for Green Chemical Technology of State Education Ministry,School of Chemical Engineering & Technology,Tianjin University3. State Key Laboratory of Engines,Tianjin University
摘 要:MnOx-CeO2 catalysts were synthesized to investigate the active sites for NO oxidation by varying the calcination temperature. XRD and TEM results showed that cubic CeO2 and amorphous MnOx existed in MnOx-CeO2 catalysts. High temperature calcination caused the sintering of amorphous MnOx and transforming to bulk crystalline Mn2O3, H2-TPR and XPS results suggested the valence of Mn in MnOx-CeO2 was higher than pure MnOx, and decreased with the increasing calcination temperature, The turnover frequency(TOF) was calculated based on the initial reducibility according to H2-TPR quantitation and kinetic study. The TOF results indicated that the initial reducibility of amorphous MnOx with high valence manganese ions was equivalent to the active sites for NO oxidation. It can be inferred that the amorphous MnOx plays a key role in low-temperature NO oxidation.
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