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Photocatalytic Activity of Nanotubular TiO2 Films Obtained by Anodic Oxidation: A Comparison in Gas and Liquid Phase

机译:阳极氧化获得的纳米管TiO2薄膜的光催化活性:气相和液相的比较。

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摘要

The availability of immobilized nanostructured photocatalysts is of great importance in the purification of both polluted air and liquids (e.g., industrial wastewaters). Metal-supported titanium dioxide films with nanotubular morphology and good photocatalytic efficiency in both environments can be produced by anodic oxidation, which avoids release of nanoscale materials in the environment. Here we evaluate the effect of different anodizing procedures on the photocatalytic activity of TiO2 nanostructures in gas and liquid phases, in order to identify the most efficient and robust technique for the production of TiO2 layers with different morphologies and high photocatalytic activity in both phases. Rhodamine B and toluene were used as model pollutants in the two media, respectively. It was found that the role of the anodizing electrolyte is particularly crucial, as it provides substantial differences in the oxide specific surface area: nanotubular structures show remarkably different activities, especially in gas phase degradation reactions, and within nanotubular structures, those produced by organic electrolytes lead to better photocatalytic activity in both conditions tested.
机译:固定化纳米结构光催化剂的可用性对于净化污染的空气和液体(例如工业废水)非常重要。可以通过阳极氧化生产在两种环境中具有纳米管形态和良好的光催化效率的金属支撑的二氧化钛薄膜,这避免了纳米级材料在环境中的释放。在这里,我们评估了不同的阳极氧化工艺对气相和液相中TiO2纳米结构的光催化活性的影响,以便确定生产两种形态和不同光催化活性的TiO2层的最有效,最可靠的技术。罗丹明B和甲苯分别用作两种介质中的模型污染物。已经发现,阳极氧化电解质的作用特别关键,因为它在氧化物比表面积上提供了很大的差异:纳米管结构表现出明显不同的活性,尤其是在气相降解反应中,以及在纳米管结构中,有机电解质产生的那些在两种测试条件下均具有更好的光催化活性。

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