Electrocatalytic degradation of sulfamethylthiadiazole by GAC@Ni/Fe three-dimensional particle electrode

电极 衍射仪 材料科学 扫描电子显微镜 X射线光电子能谱 粒子(生态学) 分析化学(期刊) 粒径 阳极 化学 化学工程 核化学 冶金 复合材料 色谱法 物理化学 工程类 地质学 海洋学
作者
Siwen Li,Yingzi Lin,Suiyi Zhu,Gen Liu
出处
期刊:Environmental Science and Pollution Research [Springer Science+Business Media]
卷期号:29 (38): 57112-57126 被引量:21
标识
DOI:10.1007/s11356-022-19021-4
摘要

In this work, GAC@Ni/Fe particle electrodes were prepared and employed for the degradation of sulfamethylthiadiazole (SMT) by three-dimensional electrocatalytic technology. The effects of particle electrode bi-metal loading ratio, cell voltage, particle electrode dosage, electrode plate spacing, and SMT initial concentration on SMT removal were studied. In addition, GAC@Ni/Fe particle electrode was analyzed by the scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffractometer (XRD), X-ray photoelectron spectrometer (XPS), and Fourier transform infrared spectrometer (FTIR) to characterize which indicated that a significant amount of iron-nickel oxide was formed on the surface of GAC@Ni/Fe particle electrode. The results indicated that when the nickel-iron loading ratio is 1:1, the SMT removal effect is the best, and the removal rate can reach 90.89% within 30 min. Compared with the granular activated carbon without bimetal, the removal efficiency is increased by 37.58%. The degradation of SMT in the GAC@Ni/Fe particle three-dimensional electrode reactor is the joint result of both direct oxidation and indirect oxidation. The contribution rates of direct oxidation of anode and particle electrode and indirect oxidation of ·OH in the degradation are 32%, 27%, and 41%, respectively. Based on the intermediate detected by ultra-high liquid chromatography and the calculation of bond energy of SMT molecule by Gauss software, the degradation pathway of SMT in the GAC@Ni/Fe three-dimensional electrode reactor is proposed. This research provides a green, healthy, and effective method for removing sulfonamide micro-polluted wastewater.
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