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Microfibrous TiO(2) supported photocatalysts prepared by metal-organic chemical vapor infiltration for indoor air and waste water purification

The photocatalytic degradation of gaseous (toluene) and aqueous (imazapyr, malic acid, orange G) pollutants over TiO(2) supported photocatalysts is investigated using a batch reactor. A strong influence of the microstructural characteristics of TiO(2) on the decomposition kinetics of the pollutants...

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Bibliographic Details
Published in:Applied catalysis. B, Environmental Environmental, 2009-09, Vol.91 (1-2), p.225-233
Main Authors: Sarantopoulos, Christos, Puzenat, Eric, Guillard, Chantal, Herrmann, Jean-Marie, Gleizes, Alain N, Maury, Francis
Format: Article
Language:English
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Summary:The photocatalytic degradation of gaseous (toluene) and aqueous (imazapyr, malic acid, orange G) pollutants over TiO(2) supported photocatalysts is investigated using a batch reactor. A strong influence of the microstructural characteristics of TiO(2) on the decomposition kinetics of the pollutants is found. Well crystallized, porous TiO(2)-anatase films grown under low pressure at 400-500 'C by MOCVD on glass plates and by MOCVI on glass micro-fibers are the best heterogeneous photocatalysts, showing the highest activity. We demonstrate a good control of these characteristics by choosing the deposition parameters. Achieving conformal coverage (i.e. good infiltration) of glass micro-fibers by the TiO(2) thin films has also a strong influence on the photocatalytic activity. A correlation between optimal infiltration, film microstructure and photocatalytic activity is established. Strong similarities between optimal photocatalytic decomposition rate in gas and liquid phase were found with respect to the film microstructure and the photocatalyst mass. The total mineralization of the toluene was prevented because of the deactivation of the photocatalyst surface. However the reactivation of the photocatalyst was achieved by UV irradiation under oxygen stream. This allows a long-term use of the photocatalyst.
ISSN:0926-3373
DOI:10.1016/j.apcatb.2009.05.029