Show simple item record

dc.contributor.authorZhu, Z.
dc.contributor.authorLi, Xin Yong
dc.contributor.authorZhao, Q.
dc.contributor.authorQu, Z.
dc.contributor.authorHou, Y.
dc.contributor.authorZhao, L.
dc.contributor.authorLiu, Shaomin
dc.contributor.authorChen, G.
dc.date.accessioned2017-01-30T12:05:55Z
dc.date.available2017-01-30T12:05:55Z
dc.date.created2016-09-12T08:36:44Z
dc.date.issued2010
dc.identifier.citationZhu, Z. and Li, X.Y. and Zhao, Q. and Qu, Z. and Hou, Y. and Zhao, L. and Liu, S. et al. 2010. FTIR study of the photocatalytic degradation of gaseous benzene over UV-irradiated TiO2 nanoballs synthesized by hydrothermal treatment in alkaline solution. Materials Research Bulletin. 45 (12): pp. 1889-1893.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/18097
dc.identifier.doi10.1016/j.materresbull.2010.09.007
dc.description.abstract

In this study, photocatalysts of TiO2 nanoballs were obtained via a hydrothermal treating of commercial P25 in alkaline solution, and then characterized with SEM, XRD, BET and surface photovoltage spectroscopy techniques. The UV-assisted photodegradation of gaseous benzene over P25 and the prepared TiO2 nanoballs was monitored by an in situ infrared technique. The results demonstrated that the prepared TiO2 nanoballs in anatase form were more active than commercial P25 in photocatalytic oxidation of gaseous benzene. The promoted activity of the hydrothermal-treated TiO 2 is attributed to the increasing specific surface area and larger band gap induced by the reduced crystallite size. The spectra of FTIR indicated that weakly adsorbed phenol was formed as the reaction progress. Hydroxyl groups on the surface of TiO2 nanoballs are able to react with photo-produced phenol, which is then retained on the catalyst surface leading to the progressive deactivation of the catalyst in the gas-solid system. © 2010 Elsevier Ltd. All rights reserved.

dc.publisherPergamon
dc.titleFTIR study of the photocatalytic degradation of gaseous benzene over UV-irradiated TiO2 nanoballs synthesized by hydrothermal treatment in alkaline solution
dc.typeJournal Article
dcterms.source.volume45
dcterms.source.number12
dcterms.source.startPage1889
dcterms.source.endPage1893
dcterms.source.issn0025-5408
dcterms.source.titleMaterials Research Bulletin
curtin.departmentDepartment of Chemical Engineering
curtin.accessStatusFulltext not available


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)

Show simple item record