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dc.contributor.authorXu, Yifanen_US
dc.contributor.authorLiu, Rongen_US
dc.contributor.authorJia, Fengen_US
dc.contributor.authorJi, Lingchenen_US
dc.contributor.authorYe, Feien_US
dc.date.accessioned2018-08-21T05:53:10Z-
dc.date.available2018-08-21T05:53:10Z-
dc.date.issued2017-12-01en_US
dc.identifier.issn1947-2935en_US
dc.identifier.urihttp://dx.doi.org/10.1166/sam.2017.3124en_US
dc.identifier.urihttp://hdl.handle.net/11536/144354-
dc.description.abstractA series of manganese oxide and cerium oxide catalysts supported on monoclinic zirconia (m-ZrO2), tetragonal zirconia (t-ZrO2) and cubic zirconia (c-ZrO2) were prepared by a wet-impregnation method. The catalytic performance and SO2 tolerance for the selective reduction (SCR) of NOx with NH3 were investigated. Measurements were carried out in a fixed-bed reactor. The results suggested that both SCR activity (NO conversion on the catalysts) and SO2 tolerance of the prepared catalysts decreased in the following order: 5 wt.% MnOx-CeO2/c-ZrO2(5c) > 5 wt.% MnOx-CeO2/t-ZrO2(5t) > 5 wt.% MnOx-CeO2/m-ZrO2(5m) Surface properties are discussed by using XRD, BET, SEM, XPS, TPR, TPD and TG-DTA, FT-IR. 5 wt.% MnOx-CeO2/c-ZrO2 catalyst exhibited the best redox property and the highest adsorption capacity for NH3 while 5 wt.% MnOx-CeO2/m-ZrO2 and 5 wt.% MnOx-CeO2/t-ZrO2 catalysts exhibited relatively poor performance. Also, there existed the largest density of acid sites and highest strength of acidity when c-ZrO2 was used as carrier. The deterioration of active component and deposition of NH4HSO4, (NH4)(2)SO4 or metallic sulfites were identified as the main causes of SO2 poisoning.en_US
dc.language.isoen_USen_US
dc.subjectSelective Catalytic Reductionen_US
dc.subjectZirconia Polymorphsen_US
dc.subjectLow Temperatureen_US
dc.subjectSO2 Poisoningen_US
dc.titleEffect of ZrO2 Crystal Structures on the Catalytic Performance of MnOx-CeO2/ZrO2 for Selective Reduction of NO with NH3 at Low Temperatureen_US
dc.typeArticleen_US
dc.identifier.doi10.1166/sam.2017.3124en_US
dc.identifier.journalSCIENCE OF ADVANCED MATERIALSen_US
dc.citation.volume9en_US
dc.citation.spage2104en_US
dc.citation.epage2113en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000419755000008en_US
Appears in Collections:Articles