完整後設資料紀錄
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dc.contributor.authorLee, Tsungyuen_US
dc.contributor.authorBai, Hsunlingen_US
dc.date.accessioned2018-08-21T05:53:33Z-
dc.date.available2018-08-21T05:53:33Z-
dc.date.issued2018-04-11en_US
dc.identifier.issn0888-5885en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.iecr.8b00511en_US
dc.identifier.urihttp://hdl.handle.net/11536/144850-
dc.description.abstractThe MnFe/TiO2 catalysts were poisoned by metal sulfates and/or ammonium sulfate to understand the SO2 poisoning effect under low-temperature selective catalytic reduction (SCR) of NO with NH3. The results showed that the formation of metal sulfates had a more serious deactivation effect than that of ammonium salts on the MnFe/TiO2 catalysts. After thermal regeneration, the metal sulfates on the catalyst could not be removed so that the NOx conversion was only recovered from 17% to 35%. On the other hand, water washing was capable to remove both ammonium salts and metal sulfates, and the NOx conversion could be recovered to 88% (compared to 99% for the fresh catalyst). The analytical results of the synchrotron-based XRD, BET, NH3-TPD, and XPS revealed that lower crystallinity, lower specific surface area, lower ratio of Mn4+/Mn3+, higher surface acidity, and more chemisorbed oxygen were the main causes for the presence of metal sulfates poisoning, which then resulted in the low NOx conversion at low temperature.en_US
dc.language.isoen_USen_US
dc.titleMetal Sulfate Poisoning Effects over MnFe/TiO2 for Selective Catalytic Reduction of NO by NH3 at Low Temperatureen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/acs.iecr.8b00511en_US
dc.identifier.journalINDUSTRIAL & ENGINEERING CHEMISTRY RESEARCHen_US
dc.citation.volume57en_US
dc.citation.spage4848en_US
dc.citation.epage4858en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000430155700011en_US
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