Numéro |
J. Phys. IV France
Volume 09, Numéro PR3, March 1999
Proceedings of the 9th SolarPACES International Symposium on Solar Thermal Concentrating TechnologiesSTCT 9 |
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Page(s) | Pr3-247 - Pr3-252 | |
DOI | https://doi.org/10.1051/jp4:1999337 |
STCT 9
J. Phys. IV France 09 (1999) Pr3-247-Pr3-252
DOI: 10.1051/jp4:1999337
Self-cleaning properties of TiO2-coated glass : Degradation, under simulated solar light, of palmitic (hexadecanoic) acid and fluoranthene layers deposited on the glass surface
V. Roméas1, P. Pichat1, C. Guillard1, T. Chopin2 and C. Lehaut21 URA au CNRS, Photocatalyse, Catalyse et Environnement, École Centrale de Lyon, BP. 163, 69131 Ecully cedex, France
2 Rhodia, Centre de Recherches, 93308 Aubervilliers cedex, France
Abstract
The self-cleaning property of glass arises from a thin transparent TiO2 coating. Under solar UV light, TiO2 becomes capable of degrading organics at its surface. Our objectives were : to assess the self-cleaning efficiency with respect to the removal of compounds representative of organic deposits ; to identify and, if possible, quantify the intermediate products formed during the destruction of these organic layers both to complete the data concerning the self-cleaning properties and to have an insight into the photocatalytic degradation pathways. Our target compounds were palmitic (hexadecanoic) acid and fluoranthene : both are present in the atmospheric solid particles and come from various sources. The removal rates of layers of these compounds sprayed on the self-cleaning glass were found to be sufficient for the expected application. The identified intermediates (about 40 for each compound) show the gradual splitting of the palmitic acid chain and the oxidative openings of the aromatic rings of fluoranthene. In the case of palmitic acid the products give some indications about the photocatalytic mechanism. About 20 % of the organic carbon contained in the initial compounds was transformed into volatile carbonyl products. In the case of fluoranthene, this percentage was less than for the degradation on TiO2-free glass.
© EDP Sciences 1999