完整後設資料紀錄
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dc.contributor.authorTsai, Cheng-Yenen_US
dc.contributor.authorHsi, Hsing-Chengen_US
dc.contributor.authorBai, Hsunlingen_US
dc.contributor.authorFan, Kuo-Shuhen_US
dc.contributor.authorChen, Chienchihen_US
dc.date.accessioned2014-12-08T15:20:45Z-
dc.date.available2014-12-08T15:20:45Z-
dc.date.issued2011-10-01en_US
dc.identifier.issn1388-0764en_US
dc.identifier.urihttp://dx.doi.org/10.1007/s11051-011-0442-8en_US
dc.identifier.urihttp://hdl.handle.net/11536/14773-
dc.description.abstractOxygen-vacant titanium dioxide (TiO(2-x) ) nanoparticles were synthesized using thermal plasma as a heating source at various applied plasma currents and He/Ar ratios. Samples with diverse characteristics were developed and the mercury removal effectiveness was subsequently evaluated. TiO(2) nanoparticles possessing high purity and uniform particle sizes were successfully synthesized using metal titanium and O(2) as precursors and Ar as plasma gas. TiO(2-x) in anatase phase with a particle size at 5-10 nm was formed at the He/Ar volume ratio of 25/75. Further increasing the He/Ar ratio elevated the plasma temperature, causing the tungsten to melt, vaporize from the cathode, and then dope into the formed TiO(2) nanoparticles. The doped W appeared to inhibit the growth of nanoparticles and decrease the crystallinity of formed anatase. The effectiveness of oxygen-vacant sites on Hg(0) removal under the visible light circumstance was confirmed. Hg(0) removal by the TiO(2-x) nanoparticles was enhanced by increasing the O(2) concentration. However, moisture reduced Hg(0) capture, especially when light irradiation was applied. The reduction in Hg(0) capture may be resulted from the competitive adsorption of H(2)O on the active sites of TiO(2-x) with Hg(0) and transformed Hg(2+).en_US
dc.language.isoen_USen_US
dc.titleTiO(2-x) nanoparticles synthesized using He/Ar thermal plasma and their effectiveness on low-concentration mercury vapor removalen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s11051-011-0442-8en_US
dc.identifier.journalJOURNAL OF NANOPARTICLE RESEARCHen_US
dc.citation.volume13en_US
dc.citation.issue10en_US
dc.citation.spage4739en_US
dc.citation.epage4748en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
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