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dc.contributor.authorWang, N.
dc.contributor.authorLi, Xin Yong
dc.contributor.authorWang, Y.
dc.contributor.authorQuan, X.
dc.contributor.authorChen, G.
dc.date.accessioned2017-01-30T11:20:34Z
dc.date.available2017-01-30T11:20:34Z
dc.date.created2016-09-12T08:36:52Z
dc.date.issued2009
dc.identifier.citationWang, N. and Li, X.Y. and Wang, Y. and Quan, X. and Chen, G. 2009. Evaluation of bias potential enhanced photocatalytic degradation of 4-chlorophenol with TiO2 nanotube fabricated by anodic oxidation method. Chemical Engineering Journal. 146 (1): pp. 30-35.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/10737
dc.identifier.doi10.1016/j.cej.2008.05.025
dc.description.abstract

TiO2 nanotube was fabricated using anodic oxidation method. The samples were characterized by scanning electron microscope (SEM), X-ray diffraction (XRD) and Brunauer-Emmett-Teller (BET). The obtained TiO2 nanotube exhibited increased photoelectrocatalytic (PEC) activities compared to TiO2 film for 4-chlorophenol (4-CP) degradation in aqueous solution. Comparing with electrochemical process (EP), direct photolysis (DP) and photocatalytic (PC), a significant PEC synergetic effect was observed. The factors influencing the degradation of 4-CP by the PEC process including bias potential, pH, initial concentration of 4-CP, UV light intensity and electrolyte concentration were examined. The results revealed that the bias potential played an important role in the degradation of 4-CP and the most efficient degradation of 4-CP was achieved in highly acidic and alkaline medium. Initial concentration of 4-CP was also a significant factor affecting the degradation of 4-CP. Moreover, the degradation rate increased with both UV light intensity and electrolyte concentration increasing. © 2008 Elsevier B.V. All rights reserved.

dc.publisherElsevier BV
dc.titleEvaluation of bias potential enhanced photocatalytic degradation of 4-chlorophenol with TiO2 nanotube fabricated by anodic oxidation method
dc.typeJournal Article
dcterms.source.volume146
dcterms.source.number1
dcterms.source.startPage30
dcterms.source.endPage35
dcterms.source.issn1385-8947
dcterms.source.titleChemical Engineering Journal
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


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