The Efficient Degradation of Oxytetracycline in Wastewater Using Fe/Mn-Modified Magnetic Oak Biochar: Pathways and Mechanistic Investigation

生物炭 降级(电信) 废水 环境化学 污水处理 土霉素 化学 环境科学 材料科学 化学工程 环境工程 热解 生物化学 计算机科学 电信 有机化学 工程类 抗生素
作者
Yujie Zhou,Y. B. Fu,Xiaoxue Niu,Bohan Wu,Xinghan Liu,Hao Fu,Zichuan Ma,Hao Cai,Yuheng Liu
出处
期刊:Magnetochemistry [MDPI AG]
卷期号:11 (6): 49-49 被引量:5
标识
DOI:10.3390/magnetochemistry11060049
摘要

Antibiotic resistance has been recognized as a global threat to human health. Therefore, it is urgent to develop effective strategies to address the contamination of water environments caused by antibiotics. In this study, Fe/Mn bimetallic-modified biochar (FMBC) was synthesized through a one-pot oxidation/reduction-hydrothermal co-precipitation method, demonstrating an exceptional photocatalytic-Fenton degradation performance for oxytetracycline (OTC). Characterization techniques including FTIR, SEM, XRD, VSM, and N2 adsorption–desorption analysis confirmed that the Fe/Mn bimetals were successfully loaded onto the surface of biochar in the form of Fe3O4 and MnFe2O4 mixed crystals and exhibited favorable paramagnetic properties that facilitate magnetic recovery. A key innovation is the utilization of biochar’s inherent phenol/quinone structures as reactive sites and electron transfer mediators, which synergistically interact with the loaded bimetallic oxides to significantly enhance the generation of highly reactive ·OH radicals, thereby boosting catalytic activity. Even after five recycling cycles, the material exhibited minimal changes in degradation efficiency and bimetallic crystal structure, indicating its notable stability and reusability. The photocatalytic degradation experiment conducted in a Fenton-like reaction system demonstrates that, under the conditions of pH 4.0, a H2O2 concentration of 5.16 mmol/L, a catalyst dosage of 0.20 g/L, and an OTC concentration of 100 mg/L, the optimal degradation efficiency of 98.3% can be achieved. Additionally, the pseudo-first-order kinetic rate constant was determined to be 4.88 min−1. Furthermore, this study elucidated the detailed degradation mechanisms, pathways, and the influence of various ions, providing valuable theoretical insights and technical support for the degradation of antibiotics in real wastewater.
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