在可见光下合成具有新型光催化活性的WO3/g-C3N4 z型异质结降解水生环境中残留抗生素

Huong Nguyen Thuy, Ha Nguyen Thi, Noi Nguyen Van, Dong Pham Thanh, Phuong Tran Thi Thu, Lan Nguyen Thi, Hien Tran Thị Thu, Cam Nguyen Thi Dieu, Trung Nguyen Tien
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引用次数: 0

摘要

在这项研究中,我们成功地合成了WO3/g-C3N4 Z-scheme异质结用于光催化降解四环素。利用x射线衍射(XRD)、扫描电镜(SEM)和傅里叶变换红外光谱(FTIR)对合成材料进行了表征,研究了它们的晶相、形貌和化学成分。合成的WO3/g-C3N4 Z-scheme异质结在可见光下对四环素的降解也表现出了新的光催化活性。这是由于WO3的导带中的光激发电子转移到g-C3N4的价带中,保留了g-C3N4的导带中的电子和WO3的价带中的空穴。这些电子和空穴与氧和水反应产生氧化自由基,有效降解四环素。合成的WO3/g-C3N4在32 W可见光照射90 min时,光催化降解约56%的四环素10 ppm。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of WO3/g-C3N4 Z-scheme heterojunction with novel photocatalytic activity for degradation of residual antibiotics in aquatic environment under visible light
In the research, we successfully synthesized WO3/g-C3N4 Z-scheme heterojunction for photocatalytic degradation of tetracycline. These synthesized materials have been characterized by X-ray diffraction (XRD), Scanning electron microscope (SEM) and Fourier transform infrared spectroscopy (FTIR Spectroscopy), to investigate their crystal phase, morphology and chemical compositions. The synthesized WO3/g-C3N4 Z-scheme heterojunction exhibited novel photocatalytic activity for the degradation of Tetracyline even under visible light. This was due to photo-excited electrons in the conduction band of WO3 transferred to the valence band of the g-C3N4 preserving electrons in the conduction band of the g-C3N4 and holes in the valence band of WO3. These electrons and holes would react with oxygen and water to produce oxidative radicals for effective degradation of Tetracycline. The synthesized WO3/g-C3N4 photocatalytically degraded approximately 56 % Tetracycline 10 ppm when it was irradiated by visible light of 32 W for 90 mins.
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