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dc.contributor.authorDen, Wen_US
dc.contributor.authorHuang, CPen_US
dc.contributor.authorKe, HCen_US
dc.date.accessioned2014-12-08T15:16:36Z-
dc.date.available2014-12-08T15:16:36Z-
dc.date.issued2006-05-10en_US
dc.identifier.issn0888-5885en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ie0514410en_US
dc.identifier.urihttp://hdl.handle.net/11536/12258-
dc.description.abstractThis study investigates the removal mechanisms involved in the monopolar, continuous-flow electrocoagulation of a polishing wastewater containing negatively charged silica particles. Using iron as the anodes, the mechanisms were inferred from the experimental observations of the changes in pH, zeta-potential, and turbidity as a function of reaction time, as well as from the sludge characterization. Two types of distinct mechanisms were observed, one involving particle destabilization by oppositely charged ferrous ions and the other involving coprecipitation or enmeshment of silica particles with the iron hydroxides. The former mechanism was apparently responsible for the formation of "surface flocs", whereas the latter one was responsible for the "sediment sludge". The sludge collected separately from the two "sinks" was distinctly different in both physical appearance and settling velocity. Furthermore, based on the sheer quantity of the surface flocs and the sediment sludge, the two mechanisms involved in the electrocoagulation process were equally important to the silica removal.en_US
dc.language.isoen_USen_US
dc.titleMechanistic study on the continuous flow electrocoagulation of silica nanoparticles from polishing wastewateren_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ie0514410en_US
dc.identifier.journalINDUSTRIAL & ENGINEERING CHEMISTRY RESEARCHen_US
dc.citation.volume45en_US
dc.citation.issue10en_US
dc.citation.spage3644en_US
dc.citation.epage3651en_US
dc.contributor.department環境工程研究所zh_TW
dc.contributor.departmentInstitute of Environmental Engineeringen_US
dc.identifier.wosnumberWOS:000237576300043-
dc.citation.woscount15-
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