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Combined TiO[sub]2/SiO[sub]2 mesoporous photocatalysts with location and phase controllable TiO[sub]2 nanoparticles

Combined TiO[sub]2/SiO[sub]2 mesoporous materials were prepared by deposition of TiO[sub]2 nanoparticles synthesised via the acid-catalysed sol-gel method. In the first synthesis step a titania solution is prepared, by dissolving titaniumtetraisopropoxide in nitric acid. The influences of the initia...

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Bibliographic Details
Published in:Applied catalysis. B, Environmental Environmental, 2009-05, Vol.88 (3-4), p.515-524
Main Authors: Beyers, E, Biermans, E, Ribbens, S, De Witte, K, Mertens, M, Meynen, V, Bals, S, Van Tendeloo, G., Vansant, E F, Cool, P
Format: Article
Language:English
Online Access:Get full text
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Summary:Combined TiO[sub]2/SiO[sub]2 mesoporous materials were prepared by deposition of TiO[sub]2 nanoparticles synthesised via the acid-catalysed sol-gel method. In the first synthesis step a titania solution is prepared, by dissolving titaniumtetraisopropoxide in nitric acid. The influences of the initial titaniumtetraisopropoxide concentration and the temperature of dissolving on the final structural properties were investigated. In the second step of the synthesis, the titania nanoparticles were deposited on a silica support. Here, the influence of the temperature during deposition was studied. The depositions were carried out on two different mesoporous silica supports, SBA-15 and MCF, leading to substantial differences in the catalytic and structural properties. The samples were analysed with N[sub]2-sorption, X-ray diffraction (XRD), electron probe microanalysis (EPMA) and transmission electron microscopy (TEM) to obtain structural information, determining the amount of titania, the crystal phase and the location of the titania particles on the mesoporous material (inside or outside the mesoporous channels). The structural differences of the support strongly determine the location of the nanoparticles and the subsequent photocatalytic activity towards the degradation of rhodamine 6G in aqueous solution under UV irradiation.
ISSN:0926-3373
DOI:10.1016/j.apcatb.2008.10.009