WO3-modified TiO2 nanotubes for photocatalytic elimination of methylethylketone under UVA and solar light irradiation
[Display omitted] ► Modification of TiO2 nanotubes with WO3 particles. ► UV-A and solar light activation. ► Optimization of the photocatalytic activity of WO3-modified TiO2 nanotubes. ► Influence of WO3 concentration on the activity and on the deactivation phenomena. ► Heterojunction formation betwe...
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Published in | Journal of photochemistry and photobiology. A, Chemistry. Vol. 245; pp. 43 - 57 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.10.2012
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Subjects | |
Online Access | Get full text |
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Summary: | [Display omitted]
► Modification of TiO2 nanotubes with WO3 particles. ► UV-A and solar light activation. ► Optimization of the photocatalytic activity of WO3-modified TiO2 nanotubes. ► Influence of WO3 concentration on the activity and on the deactivation phenomena. ► Heterojunction formation between WO3 and TiO2 semiconductors.
We report on the synthesis, the characterizations and the photocatalytic activity of WO3/TiO2 nanotubes for methylethylketone (MEK) elimination under both UVA and simulated-solar light irradiations. TiO2 nanotubes (TiNTs) were synthetized using the hydrothermal method in a concentrated 10M NaOH solution heated at 130°C during 48h, post-impregnated with tungstate salt and finally calcined. The photocatalytic efficiency for both UVA and solar light irradiation strongly depends on the WO3 content, ranging from 4 to 51wt.%. The different photocatalytic activities were analysed, in terms of initial and stabilized activities and deactivation phenomena. Complementary post-tests characterizations (TGA and XPS) aiming at the establishment of correlations between WO3 content, surface composition, surface species and the photocatalytic activity and deactivation are discussed. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1010-6030 1873-2666 |
DOI: | 10.1016/j.jphotochem.2012.06.021 |