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dc.contributor.authorLiu, Rongen_US
dc.contributor.authorXu, Yifanen_US
dc.contributor.authorYe, Feien_US
dc.contributor.authorJia, Fengen_US
dc.contributor.authorXu, Ruien_US
dc.date.accessioned2018-08-21T05:54:34Z-
dc.date.available2018-08-21T05:54:34Z-
dc.date.issued2017-10-07en_US
dc.identifier.issn1144-0546en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c7nj00775ben_US
dc.identifier.urihttp://hdl.handle.net/11536/146133-
dc.description.abstractTi-Bearing blast furnace slag has been found to be suitable as the support of the selective catalytic reduction (SCR) catalysts. Mn-Ce-M (M = Fe, Co, Ag)/Slag catalysts prepared using a solution impregnation method for the low-temperature selective catalytic reduction (SCR) of NO with NH3 under the influence of transition metals were investigated in this study. The experiments suggested that the addition of Co can greatly enhance the SCR activity and the addition of Fe can broaden the SCR temperature range (NO conversion > 90%), while the addition of Ag reduced the SCR activity. The XRD and SEM analyses revealed that for the Co and Fe doped catalysts, the active components were well dispersed, while the Ag doped catalyst had agglomeration and sintering. The XPS results revealed that the Fe and Co doped catalysts had relatively higher ratios of Mn4+/Mn3+, Ce3+/Ce4+ and O-alpha/O-alpha + O-beta. TPR results showed that the redox properties were enhanced after adding Co and Fe. NH3-TPD was also studied to investigate the acid sites over the surface of the catalysts. And the addition of Co and Fe increased strong acid sites on the surface of the catalyst. However, the strength of acid sites over the surface of the Ag doped catalyst was too high to cause the desorption of NH3.en_US
dc.language.isoen_USen_US
dc.titleInfluence of transition metal (Fe, Co, and Ag) doping on the MnOx-CeO2/Ti-bearing blast furnace slag catalyst for selective catalytic reduction of NOx with NH3 at low temperatureen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c7nj00775ben_US
dc.identifier.journalNEW JOURNAL OF CHEMISTRYen_US
dc.citation.volume41en_US
dc.citation.spage11299en_US
dc.citation.epage11307en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000411768600087en_US
Appears in Collections:Articles