完整後設資料紀錄
DC 欄位語言
dc.contributor.authorLin, Yu-Chihen_US
dc.contributor.authorBai, Hsunlingen_US
dc.contributor.authorLin, Chia-Hsinen_US
dc.contributor.authorWu, Jin-Fangen_US
dc.date.accessioned2014-12-08T15:33:43Z-
dc.date.available2014-12-08T15:33:43Z-
dc.date.issued2013-10-01en_US
dc.identifier.issn1680-8584en_US
dc.identifier.urihttp://dx.doi.org/10.4209/aaqr.2012.09.0247en_US
dc.identifier.urihttp://hdl.handle.net/11536/23310-
dc.description.abstractThis study utilized a unique method to prepare TiO2/Ag composites by operating the pH value of synthesis solution, which causes the opposite charges on the surface between TiO2 and Ag to enhance the combination affinity of TiO2 and Ag due to electron attraction. The results showed that the TiO2/Ag prepared in solution at pH 5.8 was characterized as high TiO2 dispersibility and the optimal combination between TiO2/Ag, due to the opposite surface charges and the greatest difference in zeta potentials between TiO2 and Ag. The prepared TiO2/Ag was utilized to process acetone photodegradation, and the results illustrated that TiO2/Ag prepared in solution at pH 5.8 showed the best performance in photodegrading acetone. With increasing TiO2 coated on Ag in TiO2/Ag, the photodegradation efficiency of acetone was enhanced. In terms of the average efficiency via TiO2 coating amount, 10 wt% was the most optimal efficient proportion of TiO2/Ag for the photodegradation of acetone.en_US
dc.language.isoen_USen_US
dc.subjectPhotocatalytic compositeen_US
dc.subjectPreparation procedureen_US
dc.subjectZeta potentialen_US
dc.subjectVOC photodegradationen_US
dc.titleApplying Surface Charge Attraction to Synthesizing TiO2/Ag Composition for VOCs Photodegradationen_US
dc.typeArticleen_US
dc.identifier.doi10.4209/aaqr.2012.09.0247en_US
dc.identifier.journalAEROSOL AND AIR QUALITY RESEARCHen_US
dc.citation.volume13en_US
dc.citation.issue5en_US
dc.citation.spage1512en_US
dc.citation.epage1520en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000327409400011-
dc.citation.woscount0-
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