Enhanced Fenton-like degradation of sulfadiazine by single atom iron materials fixed on nitrogen-doped porous carbon

X射线光电子能谱 催化作用 扫描电子显微镜 化学 核化学 电子顺磁共振 激进的 扫描透射电子显微镜 水溶液 碳纤维 透射电子显微镜 化学工程 无机化学 分析化学(期刊) 材料科学 有机化学 纳米技术 工程类 复合材料 物理 复合数 核磁共振
作者
Yang Wu,Peidong Hong,Dandan Yang,Ya Yang,Zijian Wu,Chao Xie,Junyong He,Kaisheng Zhang,Lingtao Kong,Jinhuai Liu
出处
期刊:Journal of Colloid and Interface Science [Elsevier]
卷期号:597: 56-65 被引量:57
标识
DOI:10.1016/j.jcis.2021.03.168
摘要

The use of single-atom iron catalysts in heterogeneous Fenton-like reactions has demonstrated tremendous potential for antibiotic wastewater treatment. In this study, single-atom iron fixed on nitrogen-doped porous carbon materials (Fe-ISAs@CN) was synthesised using a metal organic framework (MOF) as a precursor. Fe-ISAs@CN was applied as a heterogeneous Fenton catalyst to activate H2O2 for the degradation of sulfadiazine (SDZ) in an aqueous solution. The physical and chemical properties of Fe-ISAs@CN were characterised by scanning electron microscopy (SEM), transmission electron microscope (TEM), high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and rotating disk electrode (RDE) measurements. The results of our degradation experiments indicated that Fe-ISAs@CN exhibited remarkable activity and stability for the degradation of SDZ over a wide pH range; even after five cycles, Fe-ISAs@CN retained a high catalytic efficiency (>80%). The 5,5-dimethyl-1-oxaporphyrin-n-oxide (DMPO)-X signal captured by electron paramagnetic resonance (EPR) spectroscopy indicated that a large amount of hydroxyl radicals (OH) was produced in the reaction system. Quench tests indicated that the OH was the main active substance in the degradation of SDZ. The degradation products of the reaction were analysed by High Performance Liquid Chromatography-Mass Spectrometry (HPLC-MS), and possible degradation pathways for the SDZ degradation were proposed.
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