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dc.contributor.authorCetinkaya, Tugrul
dc.contributor.authorNeuwirthová, Lucie
dc.contributor.authorMamulová Kutláková, Kateřina
dc.contributor.authorTomášek, Vladimír
dc.contributor.authorAkbulut, Hatem
dc.date.accessioned2013-08-15T10:41:19Z
dc.date.available2013-08-15T10:41:19Z
dc.date.issued2013
dc.identifier.citationApplied Surface Science. 2013, vol. 279, p. 384-390.cs
dc.identifier.issn0169-4332
dc.identifier.urihttp://hdl.handle.net/10084/100619
dc.description.abstractTiO2/SiO2 composites were produced as photocatalysts both by hydrolysis of TiCl4 and from TiO2 suspension prepared by hydrolysis of TiCl4. TiO2/SiO2 composites were dried at 70 °C and calcinated at 400 °C and 600 °C to investigate the effect of calcination temperature on the phase transformation of TiO2 structure. Photocatalytic effects of produced TiO2/SiO2 composites were measured against degradation of acid orange 7 (AO7) by UV–vis spectroscopy. The chemical compositions of produced samples were studied by X-ray fluorescence (XRF) technique. The composite structures were analyzed by X-ray diffraction (XRD) pattern and scanning electron microscopy (SEM) facilities to reveal the surface morphology and their phase structures. Energy dispersive X-ray spectroscopy (EDS) was conducted to understand the elemental surface composition of composites. Photocatalytic activity of composites normalized with surface area, and TiO2/SiO2 composite produced by TiO2 suspension prepared by hydrolysis of TiCl4 and calcinated at 600 °C indicated 40% photocatalytic degradation of AO7 after 2 h under UV radiation.cs
dc.language.isoencs
dc.publisherElseviercs
dc.relation.ispartofseriesApplied Surface Sciencecs
dc.relation.urihttp://dx.doi.org/10.1016/j.apsusc.2013.04.121cs
dc.subjectTiO2/SiO2cs
dc.subjecthydrolysiscs
dc.subjectphotocatalystcs
dc.subjectacid orangecs
dc.titleSynthesis of nanostructured TiO2/SiO2 as an effective photocatalyst for degradation of acid orangecs
dc.typearticlecs
dc.identifier.locationNení ve fondu ÚK
dc.identifier.doi10.1016/j.apsusc.2013.04.121
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume279cs
dc.description.lastpage390cs
dc.description.firstpage384cs
dc.identifier.wos000320766500055


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