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dc.contributor.authorLin, CHen_US
dc.contributor.authorBai, Hen_US
dc.date.accessioned2014-12-08T15:38:32Z-
dc.date.available2014-12-08T15:38:32Z-
dc.date.issued2004-09-15en_US
dc.identifier.issn0888-5885en_US
dc.identifier.urihttp://hdl.handle.net/11536/26379-
dc.description.abstractA study of the inter-relationship between moisture, vanadia content, operation temperature, and surface acidity for a selective catalytic reduction (SCR) process for nitric oxide (NO) removal was conducted. The effects of operating parameters on the roles of Bronsted and Lewis acids acting in the SCR reaction were specified by the observed NO removal and the spectra of in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS). The results indicated that H2O competed with NH3 molecules to be adsorbed on the pure titania catalyst that contained only Lewis acid sites. However, the competition did not occur over a vanadia-based catalyst on which both Bronsted and Lewis acid sites appeared in the presence of H2O. As compared to that under dry conditions where only Lewis acid sites were found, the catalytic activity was lower under moisturized conditions even though both acids existed and there are fewer reaction sites available. It is concluded that surface acid sites are varied according to different operation conditions. Lewis acidity was dominant under the condition of low vanadia content and in the absence of H2O molecules. It is also less sensitive to temperature. In contrast, Bronsted acidity was dominant under the condition of high vanadia content and in the presence of H2O molecules, and it is highly affected by temperature.en_US
dc.language.isoen_USen_US
dc.titleAdsorption behavior of moisture over a vanadia/titania catalyst: A study for the selective catalytic reduction processen_US
dc.typeArticleen_US
dc.identifier.journalINDUSTRIAL & ENGINEERING CHEMISTRY RESEARCHen_US
dc.citation.volume43en_US
dc.citation.issue19en_US
dc.citation.spage5983en_US
dc.citation.epage5988en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000223807400002-
dc.citation.woscount8-
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