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首页> 外文期刊>Applied Catalysis, A. General: An International Journal Devoted to Catalytic Science and Its Applications >Photoelectrocatalytic destruction of organics using TiO2 as photoanode with simultaneous production of H2O2 at the cathode
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Photoelectrocatalytic destruction of organics using TiO2 as photoanode with simultaneous production of H2O2 at the cathode

机译:以TiO2为光阳极并同时在阴极生成H2O2的光电催化降解有机物

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Research on the photoelectrocatalytic (PEC) oxidation of organic contaminants, the role of cathodes during photocatalysis has usually been disregarded. This paper reports a study of the PEC decomposition of aniline and salicylic acid with simultaneous production of hydrogen peroxide in a divided reactor using TiO2 as a photoanode. Two types of TiO2 electrode were used. Thermal oxidation electrodes (TO-TiO2) were made by oxidation of titanium metal sheet; sol-gel electrodes (SG-TiO2) were made by coating and then heating a layer of titania gel on titanium sheet. Saturated photocurrent was used to carry out an initial characterization and optimization of both electrode types. The best TO-TiO2 electrodes were prepared by heating titanium at 600-700 degrees C in air. For the SG-TiO2 electrodes, optimum performance was obtained by heating at 500 degrees C. These electrodes were then used to photodegrade aniline and salicylate. The SG-TiO2 electrodes turned out to be superior to the TO-TiO2 electrodes in terms of PEC rate under the same conditions but the difference in rate between the two electrodes was comparable under a high enough bias potential. The most important factors affecting the production of H2O2 in the cathode compartment are presented. The current efficiencies for the accumulation of H2O2 were remarkably affected by the cathode used, PH value, cur-rent density, and metal cations such as copper and iron ions. An expected H2O2 concentration could be obtained by controlling either the magnitude of the photocurrent or illumination time. The maximum current efficiency for the cathodic reduction of oxygen to H2O2 was as high as 90.1% when graphite was used as the cathode. Compared to the SG-TiO2 electrode, the TO-TiO2 electrode had a higher light to electricity conversion efficiency, thus it turned out to be more suitable for the production of H2O2. Furthermore, the role of in-situ reduced oxygen species in the PEC decomposition of aniline was evaluated. (c) 2005 Elsevier B.V. All rights reserved.
机译:关于有机污染物的光电催化(PEC)氧化的研究,通常忽略了阴极在光催化过程中的作用。本文报道了在以TiO2为光阳极的分流反应器中苯胺和水杨酸的PEC分解同时生成过氧化氢的研究。使用了两种类型的TiO2电极。热氧化电极(TO-TiO2)是通过钛金属板的氧化制成的。溶胶-凝胶电极(SG-TiO2)的制备方法是先在钛板上涂覆一层二氧化钛凝胶,然后加热。饱和光电流用于两种电极类型的初始表征和优化。最好的TO-TiO2电极是通过在空气中在600-700摄氏度下加热钛来制备的。对于SG-TiO2电极,通过在500摄氏度下加热可获得最佳性能。然后将这些电极用于光降解苯胺和水杨酸盐。在相同条件下,SG-TiO2电极在PEC速率方面优于TO-TiO2电极,但在足够高的偏置电势下,两个电极之间的速率差异是可比的。介绍了影响阴极室中H2O2产生的最重要因素。所使用的阴极,PH值,电流密度和金属阳离子(例如铜和铁离子)会显着影响H2O2累积的电流效率。可以通过控制光电流的大小或照明时间来获得预期的H2O2浓度。当使用石墨作为阴极时,将氧气阴极还原为H2O2的最大电流效率高达90.1%。与SG-TiO2电极相比,TO-TiO2电极具有更高的光电转换效率,因此,它更适合于生产H2O2。此外,评估了原位还原氧物种在苯胺的PEC分解中的作用。 (c)2005 Elsevier B.V.保留所有权利。

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