School of Chemistry and Chemical Engineering, Guangxi University, 530004, Nanning, PR China; National Key Laboratory of Non-Food Biomass Energy Technology, Guangxi Key Laboratory of Bio-Refinery, Institute of Eco-Environmental Research, Guangxi Academy of Sciences, 98 Daling Road, 530007, Nanning, PR China.
School of Chemistry and Chemical Engineering, Guangxi University, 530004, Nanning, PR China.
Chemosphere. 2024 Jul;359:142286. doi: 10.1016/j.chemosphere.2024.142286. Epub 2024 May 8.
Antibiotics are emerging organic pollutants that have attracted huge attention owing to their abundant use and associated ecological threats. The aim of this study is to develop and use photocatalysts to degrade antibiotics, including tetracycline (TC), ciprofloxacin (CIP), and amoxicillin (AMOX). Therefore, a novel Z-scheme heterojunction composite of g-CN (gCN) and 3D flower-like BiWO (BW) perovskite structure was designed and developed, namely BiWO/g-CN (BW/gCN), which can degrade low-concentration of antibiotics in aquatic environments under visible light. According to the Density Functional Theory (DFT) calculation and the characterization results of X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FITR), Scanning electron microscopy - energy spectroscopy (SEM-EDS) and X-ray photoelectron spectroscopy (XPS), this heterojunction was formed in the recombination process. Furthermore, the results of 15 wt%-BW/gCN photocatalytic experiments showed that the photodegradation rates (Rp) of TC, CIP, and AMOX were 92.4%, 90.1% and 82.3%, respectively, with good stability in three-cycle photocatalytic experiments. Finally, the quenching experiment of free radicals showed that the holes (h) and superoxide radicals (·O) play a more important role than the hydroxyl radicals (·OH) in photocatalysis. In addition, a possible antibiotic degradation pathway was hypothesized on the basis of High performance liquid chromatography (HPLC) analysis. In general, we have developed an effective catalyst for photocatalytic degradation of antibiotic pollutants and analyzed its photocatalytic degradation mechanism, which provides new ideas for follow-up research and expands its application in the field of antibiotic composite pollution prevention and control.
抗生素是新兴的有机污染物,由于其大量使用及其相关的生态威胁,引起了人们的广泛关注。本研究旨在开发和使用光催化剂来降解抗生素,包括四环素 (TC)、环丙沙星 (CIP) 和阿莫西林 (AMOX)。因此,设计并开发了一种新型的 g-CN (gCN) 和 3D 花状 BiWO (BW) 钙钛矿结构的 Z 型异质结复合材料,即 BiWO/g-CN (BW/gCN),它可以在可见光下降解水环境中的低浓度抗生素。根据密度泛函理论 (DFT) 计算和 X 射线衍射 (XRD)、傅里叶变换红外光谱 (FITR)、扫描电子显微镜 - 能谱 (SEM-EDS) 和 X 射线光电子能谱 (XPS) 的表征结果,这种异质结在重组过程中形成。此外,15wt%-BW/gCN 光催化实验结果表明,TC、CIP 和 AMOX 的光降解率 (Rp) 分别为 92.4%、90.1%和 82.3%,在三周期光催化实验中具有良好的稳定性。最后,自由基猝灭实验表明,空穴 (h) 和超氧自由基 (·O) 在光催化中比羟基自由基 (·OH) 发挥更重要的作用。此外,根据高效液相色谱 (HPLC) 分析,提出了一种可能的抗生素降解途径。总的来说,我们开发了一种有效的抗生素污染物光催化降解催化剂,并分析了其光催化降解机制,为后续研究提供了新的思路,并扩展了其在抗生素复合污染防治领域的应用。