锐钛型二氧化钛涂层光催化降解亚甲基蓝

Nikolai Desch, Angela Rheindorf, Cornelia Fassbender, Marc Sloot, Markus Lake
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引用次数: 0

摘要

光催化涂层具有通过高级氧化工艺(AOP)促进水净化的潜力[1]。分析特定反应器类型的光催化性能机理的常用方法是记录含有亚甲基蓝的溶液中的降解行为。然而,由于亚甲基蓝相当不稳定,因此应严格看待降解结果。在这项工作中,通过各种不同的光源,研究了在涂有锐钛矿型光催化二氧化钛(TiO2)的石英玻璃表面上亚甲蓝测试溶液的降解行为。涂层是通过物理气相沉积(PVD)沉积的,采用的是反应脉冲直流磁控溅射离子镀(MSIP)方法[2],石英玻璃外侧涂有 100 nm 厚的 TiO2 涂层。所有使用 TiO2 的实验都使用了相同的玻璃。在测定降解率时,还使用了不带任何涂层的纯石英玻璃进行了额外的实验,从而可以考察不同光源对亚甲基蓝降解率的影响。本研究使用了三种不同的光源,即紫外线-A、紫外线-C 和简单的荧光灯。在整个实验过程中,亚甲基蓝的浓度由光分光计以 10 分钟为单位进行记录,所有实验均持续 24 小时。我们的数据表明,亚甲基蓝测试是一种较差的方法,因为测试物质的稳定性较低,降解率无法明确区分。如果不包括无催化剂情况下的参考测试,数据可能会被误读。本文受版权保护,保留所有权利。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Photocatalytic degradation of methylene blue by anatase TiO2 coating

Photocatalytic coatings have the potential to contribute to the purification of water via an advanced oxidation process (AOP). A commonly used method for analyzing the mechanism of the photocatalytic performance of a given reactor type is to document the degradation behavior in a solution containing methylene blue. However, since methylene blue is rather unstable, the degradation results should be viewed critically. In this work, the degradation behavior of a test solution with methylene blue on quartz glass surfaces coated with photocatalytic titanium dioxide (TiO2) of the anatase modification was investigated through a variety of different light sources. The coating was deposited by physical vapor deposition (PVD) with the reactive pulsed DC magnetron sputtering ion plating (MSIP) method described in the study by Desch and Lake, while the quartz glasses were coated with a 100 nm thick TiO2 coating on the outside. The same glasses were used for all experiments with TiO2. In the determination of the degradation rate, additional experiments were performed using pure quartz glass without any coating, which made it possible to examine the influence of different light sources on the degradation rate of methylene blue in general. Three different light sources, namely UV-A, UV-C, and simple fluorescent lamps were used in this study. The concentration of methylene blue was recorded by photo spectrometer in 10-min increments throughout the experiment and the experiments were performed for 24 h in all cases. Our data indicates that the methylene blue test is a poor method because the degradation rate is not clearly differentiable due to the low stability of the test substance. Without including reference testing in the absence of a catalyst, data may be subject to misinterpretation.

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