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dc.contributor.authorChang, CPen_US
dc.contributor.authorChen, JNen_US
dc.contributor.authorLu, MCen_US
dc.contributor.authorYang, HYen_US
dc.date.accessioned2014-12-08T15:19:44Z-
dc.date.available2014-12-08T15:19:44Z-
dc.date.issued2005-02-01en_US
dc.identifier.issn0045-6535en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.chemosphere.2004.09.072en_US
dc.identifier.urihttp://hdl.handle.net/11536/14018-
dc.description.abstractThe heterogeneous photocatalytic oxidation of gaseous N,N'-dimethylformamide (DMF) widely used in the manufacture of synthetic leather and synthetic textile was investigated. The experiments were carried out in a plug flow annular photoreactor coated with Degussa P-25 TiO2. The oxidation rate was dependent on DMF concentration, reaction temperature, water vapor, and oxygen content. Photocatalytic deactivation was observed in these reactions. The Levenspiel deactivation kinetic model was used to describe the decay of catalyst activity. Fourier transform infrared (FTIR) was used to characterize the surface and the deactivation mechanism of the photocatalyst. Results revealed that carbonylic acids, aldehydes, amines, carbonate and nitrate were adsorbed on the TiO2 surface during the photocatalytic reaction. The ions, NH4+ and NO3-, causing the deactivation of catalysts were detected on the TiO2 surface. Several treatment processes were applied to find a suitable procedure for the regeneration of catalytic activity. Among these procedures, the best one was found to be the H2O2/UV process. (C) 2004 Elsevier Ltd. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectphotocatalysisen_US
dc.subjecttitanium dioxideen_US
dc.subjectN,N'-dimethylformamideen_US
dc.subjectdeactivationen_US
dc.subjectregenerationen_US
dc.titlePhotocatalytic oxidation of gaseous DMF using thin film TiO2 photocatalysten_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.chemosphere.2004.09.072en_US
dc.identifier.journalCHEMOSPHEREen_US
dc.citation.volume58en_US
dc.citation.issue8en_US
dc.citation.spage1071en_US
dc.citation.epage1078en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000227209700008-
dc.citation.woscount20-
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