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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Microfibrous TiO2 supported photocatalysts prepared by metal-organic chemical vapor infiltration for indoor air and waste water purification
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Microfibrous TiO2 supported photocatalysts prepared by metal-organic chemical vapor infiltration for indoor air and waste water purification

机译:金属有机化学蒸汽渗透法制备的TiO2微纤维负载光催化剂,用于室内空气和废水净化

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摘要

The photocatalytic degradation of gaseous (toluene) and aqueous (imazapyr, malic acid, orange G) pollutants over TiO2 supported photocatalysts is investigated using a batch reactor. A strong influence of the microstructural characteristics of TiO2 on the decomposition kinetics of the pollutants is found. Well crystallized, porous TiO2-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 TiO2 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.
机译:使用间歇式反应器研究了TiO2负载光催化剂对气态(甲苯)和水性(咪唑并,苹果酸,橙G)污染物的光催化降解。发现TiO 2的微结构特征对污染物的分解动力学有强烈影响。在玻璃板上通过MOCVD在玻璃板上和在玻璃微纤维上通过MOCVI在400-500°C的低压下生长的结晶良好的多孔TiO2锐钛矿薄膜是最好的非均相光催化剂,表现出最高的活性。通过选择沉积参数,我们证明了对这些特性的良好控制。 TiO 2薄膜实现玻璃微纤维的保形覆盖(即良好的渗透)对光催化活性也有很大的影响。建立了最佳渗透,膜微结构与光催化活性之间的关系。关于膜的微观结构和光催化剂的质量,发现气相和液相中最佳光催化分解速率之间有很强的相似性。由于光催化剂表面的失活,防止了甲苯的总矿化。然而,光催化剂的再活化是通过在氧气流下进行紫外线照射实现的。这允许长期使用光催化剂。

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