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首页> 外文期刊>Environmental Science & Technology >Sequential Process Combination of Photocatalytic Oxidation and Dark Reduction for the Removal of Organic Pollutants and Cr(VI) using Ag/TiO_2
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Sequential Process Combination of Photocatalytic Oxidation and Dark Reduction for the Removal of Organic Pollutants and Cr(VI) using Ag/TiO_2

机译:Ag / TiO_2光催化氧化与暗还原的顺序过程组合以去除有机污染物和Cr(VI)

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摘要

We investigated a sequential photocatalysis-dark reaction, wherein organic pollutants were degraded on Ag/TiO_2 under UV irradiation and the dark reduction of hexavalent chromium (Cr(VI)) was subsequently followed. The photocatalytic oxidation of 4-chlorophenol (4-CP), a test organic substrate, induced the generation of degradation intermediates and the storage of electrons in Ag/TiO_2 which were then utilized for reducing Cr(Vl) in the postirradiation period. The dark reduction efficiency of Cr(VI) was much higher with Ag/TiO_2 (87%), compared with bare TiO_2 (27%) and Pt/TiO_2 (22%). The Cr(Vl) removal by Ag/TiO_2 (87%) was contributed by adsorption (31%), chemical reduction by intermediates of 4-CP degradation (26%), and reduction by electrons stored in Ag (30%). When formic acid, humic acid or ethanol was used as an alternative organic substrate, the electron storage effect was also observed. The postirradiation removal of Cr(VI) on Ag/TiO_2 continued for hours, which is consistent with the observation that a residual potential persisted on the Ag/ TiO_2 electrode in the dark whereas little residual potential was observed on bare TiO_2 and Pt/TiO_2 electrodes. The stored electrons in Ag/TiO_2 and their transfer to Cr(VI) were also indicated by the UV-visible absorption spectral change. Moreover, the electrons stored in the preirradiated Ag/TiO_2 reacted with O_2 with showing a sign of low-level OH radical generation in the dark period.
机译:我们研究了顺序的光催化-暗反应,其中有机污染物在紫外线辐射下在Ag / TiO_2上降解,随后跟随六价铬(Cr(VI))的暗还原。测试有机底物4-氯苯酚(4-CP)的光催化氧化诱导了降解中间体的产生和电子在Ag / TiO_2中的存储,然后在辐照后阶段将其用于还原Cr(VI)。与裸露的TiO_2(27%)和Pt / TiO_2(22%)相比,Ag / TiO_2(87%)对Cr(VI)的暗还原效率要高得多。 Ag / TiO_2去除Cr(VI)(87%)的原因是吸附(31%),4-CP降解中间体的化学还原(26%)和银中存储的电子的还原(30%)。当使用甲酸,腐殖酸或乙醇作为替代有机底物时,也观察到电子存储效果。 Ag / TiO_2上的Cr(VI)在辐照后的去除持续了数小时,这与以下观察结果一致:在黑暗中Ag / TiO_2电极上仍残留有残余电位,而在裸露的TiO_2和Pt / TiO_2电极上观察到的残余电位很小。 UV /可见光吸收光谱的变化也表明了Ag / TiO_2中所存储的电子及其向Cr(VI)的转移。此外,存储在预辐照的Ag / TiO_2中的电子与O_2反应,在暗期显示出低水平的OH自由基生成的迹象。

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  • 来源
    《Environmental Science & Technology》 |2017年第7期|3973-3981|共9页
  • 作者单位

    Department of Chemical Engineering and Division of Environmental Science and Engineering, Pohang University of Science and Technology (POSTECH), Pohang, Korea 37673;

    Department of Chemical Engineering and Division of Environmental Science and Engineering, Pohang University of Science and Technology (POSTECH), Pohang, Korea 37673;

    Department of Chemical Engineering and Division of Environmental Science and Engineering, Pohang University of Science and Technology (POSTECH), Pohang, Korea 37673;

    Department of Chemical Engineering and Division of Environmental Science and Engineering, Pohang University of Science and Technology (POSTECH), Pohang, Korea 37673;

    Laboratory "Photoactive Nanocomposite Materials" Saint-Petersburg State University, Saint-Petersburg, Russia and "Photocatalysis and Nanotechnology", Institut fuer Technische Chemie, Gottfried Wilhelm Leibniz Universitaet Hannover, Hannover, Germany;

    Department of Chemical Engineering and Division of Environmental Science and Engineering, Pohang University of Science and Technology (POSTECH), Pohang, Korea 37673;

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