用于光-芬顿降解盐酸四环素的强磁 p-n 异质结 Fe3O4-FeWO4

Catalysts Pub Date : 2024-07-14 DOI:10.3390/catal14070453
Binger Bai, Guanrong Cheng, Jian Chen, Xiaoping Chen, Qizhao Wang
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引用次数: 0

摘要

随着抗生素的滥用,其污染对环境和人类健康的威胁与日俱增。有效降解水体中的有机污染物迫在眉睫。与传统的处理方法相比,近年来迅速发展起来的高级氧化工艺更加环保、高效,适用于更多的有机化合物。本研究采用 FeWO4 作为铁基半导体材料,对材料进行改性和优化设计。采用两步水热法制备了 Fe3O4/FeWO4 复合材料。通过 XRD、XPS、UV-vis、SEM、EDS 和 Mott-Schottky 分析了复合半导体的晶体结构、表面形貌、电化学性能和分离性。结果表明,当初始污染物浓度为 30 mg/L、初始溶液 pH 值为 4、催化剂用量为 25 mg、过氧化氢用量为 30 μL 时,盐酸四环素(TCH)在 60 min 内的降解效率可达 91%,与单一半导体 Fe3O4 和 FeWO4 相比性能有显著提高。此外,本实验制备的催化剂在实际应用中很容易通过磁分离技术进行回收,不会影响水的浑浊度,同时降低了催化剂分离和回收的成本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Strong Magnetic p-n Heterojunction Fe3O4-FeWO4 for Photo-Fenton Degradation of Tetracycline Hydrochloride
With the abuse of antibiotics, its pollution poses an increasing threat to the environment and human health. Effective degradation of organic pollutants in water bodies is urgent. Compared to traditional treatment methods, advanced oxidation processes that have developed rapidly in recent years are more environmentally friendly, efficient and applicable to a wider range of organic compounds. FeWO4 was used in this study as the iron-based semiconductor material to modify and optimize the material design. Fe3O4/FeWO4 composites were prepared by a two-step hydrothermal method. The crystal structure, surface morphology, electrochemical properties and separability of the composite semiconductor were analyzed by XRD, XPS, UV-vis, SEM, EDS and Mott-Schottky. The results showed that, when the initial contaminant concentration was 30 mg/L, the initial solution pH was 4, the dosage of the catalyst was 25 mg and the dosage of hydrogen peroxide was 30 μL, the degradation efficiency of tetracycline hydrochloride (TCH) could reach 91% within 60 min, which was significantly improved compared to the performance of the single semiconductors Fe3O4 and FeWO4. In addition, the catalyst prepared in this experiment can be easily recovered by magnetic separation technology in practical application, which will not affect the turbidity of water while reducing the cost of catalyst separation and recovery.
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