用于光催化水处理的电化学纳米二氧化钛涂层碳化硅膜:制备、表征和羟基自由基的形成

Sarah Trepte, Claudia Kutzer-Schulze, Ulrike Langklotz, Mario Krug
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摘要

基于纳米二氧化钛(TiO2)涂层的光催化活性陶瓷平板膜被生产出来,用于光催化水处理。纳米二氧化钛层是通过在碳化硅(SiC)膜上磁控溅射薄钛层,然后进行电化学氧化(阳极氧化)和随后的热处理的新颖组合制成的。拉曼光谱和场发射扫描电子显微镜的表征证明,膜上存在纳米结构的锐钛矿层。利用阳极氧化曲线、环伏安法测量以及在 UV-A 照射下定量测定水中产生的羟基自由基 (OH-),研究了钛层厚度对 TiO2 形成过程和光催化特性的影响。结果表明,纳米二氧化钛涂层膜具有良好的光催化活性和渗透性。至少 2 μm 的钛层是产生显著光催化效果的必要条件。具有 10 μm Ti/TiO2 层的膜样品具有最高的光催化活性,其形成率为 1.26 × 10-6 mmol OH- s-1。此外,还对膜进行了多次测试,观察到自由基的形成有所减少。假定这可能是反应物在二氧化钛表面的吸附过程造成的,我们进行了初步实验,以重新激活光催化器。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrochemically produced nano-TiO2-coated SiC membranes for photocatalytic water treatment: Preparation, characterization, and hydroxyl radical formation
Photocatalytically active ceramic flat sheet membranes based on a nanostructured titanium dioxide (TiO2) coating were produced for photocatalytic water treatment. The nano-TiO2 layer was produced by a novel combination of magnetron sputtering of a thin titanium layer on silicon carbide (SiC) membranes, followed by electrochemical oxidation (anodization) and subsequent heat treatment. Characterization by Raman spectra and field emission scanning electron microscopy proved the presence of a nanostructured anatase layer on the membranes. The influence of the titanium layer thickness on the TiO2 formation process and the photocatalytic properties were investigated using anodization curves, by using cyclovoltammetry measurements, and by quantifying the generated hydroxyl radicals (OH•) under UV-A irradiation in water. Promising photocatalytic activity and permeability of the nano-TiO2-coated membranes could be demonstrated. A titanium layer of at least 2 μm was necessary for significant photocatalytic effects. The membrane sample with a 10 μm Ti/TiO2 layer had the highest photocatalytic activity showing a formation rate of 1.26 × 10−6 mmol OH• s−1. Furthermore, the membranes were tested several times, and a decrease in radical formation was observed. Assuming that these can be attributed to adsorption processes of the reactants on the TiO2 surface, initial experiments were carried out to reactivate the photocatalyzer.
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