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Study on the Visible-Light Photocatalytic Performance and Degradation Mechanism of Diclofenac Sodium under the System of Hetero-Structural CuBi2O4/Ag3PO4 with H2O2

机译:CuBi2O4 / Ag3PO4与H2O2体系下双氯芬酸钠的可见光催化降解性能研究

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摘要

Two kinds of CuBi2O4/Ag3PO4 with different heterojunction structures were prepared based on the combination of hydrothermal and in-situ precipitation methods with surfactant additives (sodium citrate and sodium stearate), and their characteristics were systematically resolved by X-ray Diffraction (XRD), Brunauer–Emmett–Teller (BET), X-ray Photoelectron Spectroscopy (XPS), Scanning Electron Microscope (SEM)/ High-resolution Transmission Electron Microscopy (HRTEM), UV-vis Diffuse Reflectance Spectra (DRS) and Photoluminescence (PL). Meanwhile, the photocatalytic properties of the catalysts were determined for diclofenac sodium (DS) degradation and the photocatalytic mechanism was also explored. The results indicate that both of the two kinds of CuBi2O4/Ag3PO4 exhibit higher photocatalytic efficiency, mineralization rate, and stability than that of pure CuBi2O4 or Ag3PO4. Moreover, the catalytic activity of CuBi2O4/Ag3PO4 can be further enhanced by adding H2O2. The free radical capture experiments show that in the pure CuBi2O4/Ag3PO4 photocatalytic system, the OH and O2•− are the main species participating in DS degradation; however, in the CuBi2O4/Ag3PO4 photocatalytic system with H2O2, all OH, h+, and O2•− take part in the DS degradation, and the contribution order is OH > h+ > O2•−. Accordingly, the photocatalytic mechanism of CuBi2O4/Ag3PO4 could be explained by the Z-Scheme theory, while the catalysis of CuBi2O4/Ag3PO4 with H2O2 follows the heterojunction energy band theory.
机译:基于水热法和原位沉淀法与表面活性剂添加剂(柠檬酸钠和硬脂酸钠)的组合,制备了两种具有不同异质结结构的CuBi2O4 / Ag3PO4,并通过X射线衍射(XRD)系统地解析了它们的特性, Brunauer–Emmett–Teller(BET),X射线光电子能谱(XPS),扫描电子显微镜(SEM)/高分辨率透射电子显微镜(HRTEM),紫外可见漫反射光谱(DRS)和光致发光(PL)。同时,测定了催化剂对双氯芬酸钠(DS)降解的光催化性能,并探讨了其光催化机理。结果表明,两种CuBi2O4 / Ag3PO4均比纯CuBi2O4或Ag3PO4表现出更高的光催化效率,矿化速率和稳定性。此外,加入H 2 O 2 可以进一步提高CuBi2O4 / Ag3PO4的催化活性。自由基捕获实验表明,在纯CuBi 2 O 4 / Ag 3 PO 4 光催化体系中, OH 和O 2 •-是参与DS降解的主要物种。然而,在CuBi 2 O 4 / Ag 3 PO 4 光催化体系中,H 2 < / sub> O 2 ,所有OH ,h + 和O 2 •-< / sup>参与DS降解,其贡献顺序为OH + 2 •-< / sup>。因此,Z-可以解释CuBi 2 O 4 / Ag 3 PO 4 的光催化机理。方案论,同时用H 2催化CuBi 2 O 4 / Ag 3 PO 4 O 2 遵循异质结能带理论。

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