TiO2 deactivation during gas-phase photocatalytic oxidation of ethanol

被引:99
作者
Piera, E [1 ]
Ayllón, JA [1 ]
Doménech, X [1 ]
Peral, J [1 ]
机构
[1] Univ Autonoma Barcelona, Dept Quim, Bellaterra 08193, Spain
关键词
TiO(2); photocatalysis; ethanol;
D O I
10.1016/S0920-5861(02)00224-9
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The deactivation of TiO(2) Degussa P25 during the gas-phase photocatalytic oxidation of ethanol has been studied. Water vapor plays a clear competitive role for surface sites adsorption, thus hampering the ethanol photo-oxidation. Dark adsorption of ethanol on a fresh catalyst shows a Langmuirian behavior with the formation of a monolayer of adsorbate. Dark adsorption in a TiO(2) surface that has been used in consecutive photocatalytic experiments of ethanol degradation gives non-Langmuirian isotherms, indicating the existence of noticeable changes of the catalyst surface structure. After several irradiations the catalyst activity decreases. Such deactivation has been investigated, observing that the rate constant of ethanol and acetaldehyde (its main degradation product) oxidation decreases with irradiation time. Several surface treatments have been studied in order to find suitable procedures for catalytic activity recovery, but regular decay of activity is always observed after every treatment. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:259 / 270
页数:12
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