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dc.contributor.authorZhu, Z.
dc.contributor.authorZhao, Q.
dc.contributor.authorLi, X.
dc.contributor.authorLi, H.
dc.contributor.authorTade, Moses
dc.contributor.authorLiu, Shaomin
dc.date.accessioned2017-01-30T15:14:53Z
dc.date.available2017-01-30T15:14:53Z
dc.date.created2014-01-12T20:01:12Z
dc.date.issued2013
dc.identifier.citationZhu, Zhengru and Zhao, Qidong and Li, Xinyong and Li, Hong and Tade, Moses and Liu, Shaomin. 2013. Photocatalytic performances and activities in Ag-doped ZnAl2O4 nanorods studied by FTIR spectroscopy. Catalysis Science & Technology. 2013 (3): pp. 788-796.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/44561
dc.identifier.doi10.1039/c2cy20377d
dc.description.abstract

Porous and rod-shaped nanostructures of ZnAl2O4 were successfully synthesized by a simple hydrothermal method. The Ag-doped ZnAl2O4 catalyst, based on porous ZnAl2O4, was prepared by the incipient wetness impregnation strategy and showed an excellent photoelectric property and catalytic activity. The structural properties of the samples were systematically investigated by X-ray powder diffraction (XRD), Brunauer–Emmet–Teller (BET), transmission electron microscopy (TEM), Electron spin resonance (ESR), X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FT-IR) techniques. The photocatalytic degradation of toluene by the Ag-doped ZnAl2O4, ZnAl2O4 and P25 TiO2 samples was comparatively studied under UV lamp irradiation. The results indicate that theAg-doped ZnAl2O4 sample synthesized at pH = 6 exhibited a higher capacity for the degradation of toluene. No obvious deactivation of the Ag-doped ZnAl2O4 nanorods was observed during the prolonged operation of 6 h. The Ag-doped ZnAl2O4 nanorods could be potentially applied in environmental purification in the near future.

dc.publisherR S C Publications
dc.titlePhotocatalytic performances and activities in Ag-doped ZnAl2O4 nanorods studied by FTIR spectroscopy
dc.typeJournal Article
dcterms.source.volume394
dcterms.source.startPage788
dcterms.source.endPage796
dcterms.source.issn2044-4753
dcterms.source.titleCatalysis Science & Technology
curtin.department
curtin.accessStatusFulltext not available


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