MnO_x-CeO_2 catalysts were synthesized to investigate the active sites for NO oxidation by varying the calcination temperature. XRD and TEM results showed that cubic CeO_2 and amorphous MnO_x existed in MnO_x-CeO_2 ca...MnO_x-CeO_2 catalysts were synthesized to investigate the active sites for NO oxidation by varying the calcination temperature. XRD and TEM results showed that cubic CeO_2 and amorphous MnO_x existed in MnO_x-CeO_2 catalysts. High temperature calcination caused the sintering of amorphous MnO_x and transforming to bulk crystalline Mn_2O_3, H_2-TPR and XPS results suggested the valence of Mn in MnO_x-CeO_2 was higher than pure MnO_x, and decreased with the increasing calcination temperature, The turnover frequency（TOF） was calculated based on the initial reducibility according to H_2-TPR quantitation and kinetic study. The TOF results indicated that the initial reducibility of amorphous MnO_x with high valence manganese ions was equivalent to the active sites for NO oxidation. It can be inferred that the amorphous MnO_x plays a key role in low-temperature NO oxidation.展开更多
MnOx-CeO2 mixed oxide catalysts for methane combustion were prepared with co-precipitation me-thod.With the same content of Mn,the modified catalysts were gained via adding KMnO4.These catalysts were characterized wit...MnOx-CeO2 mixed oxide catalysts for methane combustion were prepared with co-precipitation me-thod.With the same content of Mn,the modified catalysts were gained via adding KMnO4.These catalysts were characterized with XRD,LRS,XPS and TPR techniques,respectively.It was found that the solid solution structures of the catalysts were reserved,while the low-temperature activities were promoted remarkably duo to more Mn4+ species and easier reductions through properly changing the adding amounts of Mn(NO3)2 and KMnO4.With a molar ratio of 1:4,the MnOx-CeO2 catalyst exhibited the highest activity,over which methane conversion reached 90% at a temperature as low as 390 ℃,and a better stability.展开更多
基金Project supported by the National key research and development program(2016YFC0204901)the National Natural Science Foundation of China(21576207)the introduction of talent and technology cooperation plan of Tianjin(14RCGFGX00849)
文摘MnO_x-CeO_2 catalysts were synthesized to investigate the active sites for NO oxidation by varying the calcination temperature. XRD and TEM results showed that cubic CeO_2 and amorphous MnO_x existed in MnO_x-CeO_2 catalysts. High temperature calcination caused the sintering of amorphous MnO_x and transforming to bulk crystalline Mn_2O_3, H_2-TPR and XPS results suggested the valence of Mn in MnO_x-CeO_2 was higher than pure MnO_x, and decreased with the increasing calcination temperature, The turnover frequency（TOF） was calculated based on the initial reducibility according to H_2-TPR quantitation and kinetic study. The TOF results indicated that the initial reducibility of amorphous MnO_x with high valence manganese ions was equivalent to the active sites for NO oxidation. It can be inferred that the amorphous MnO_x plays a key role in low-temperature NO oxidation.
文摘MnOx-CeO2 mixed oxide catalysts for methane combustion were prepared with co-precipitation me-thod.With the same content of Mn,the modified catalysts were gained via adding KMnO4.These catalysts were characterized with XRD,LRS,XPS and TPR techniques,respectively.It was found that the solid solution structures of the catalysts were reserved,while the low-temperature activities were promoted remarkably duo to more Mn4+ species and easier reductions through properly changing the adding amounts of Mn(NO3)2 and KMnO4.With a molar ratio of 1:4,the MnOx-CeO2 catalyst exhibited the highest activity,over which methane conversion reached 90% at a temperature as low as 390 ℃,and a better stability.
基金supported by the National High Technology Research and Development Program of China(863 Program,2013AA065304)the Open Object for Green Catalysis and Key Laboratory of Sichuan Provincial University(2013LF3004)~~
