Advanced oxidative degradation of sulfamethoxazole by using bowl-like FeCuS@Cu2S@Fe0 catalyst to efficiently activate peroxymonosulfate

催化作用 化学 降级(电信) X射线光电子能谱 电子顺磁共振 核化学 动力学 反应速率常数 激进的 质谱法 光化学 化学工程 色谱法 有机化学 电信 物理 核磁共振 量子力学 计算机科学 工程类
作者
Xiaobo Wang,Yu Zhou,Sylvestre Ndayiragije,Nan Wang,Heqing Tang,Lihua Zhu
出处
期刊:Journal of Environmental Sciences-china [Elsevier]
卷期号:126: 348-364 被引量:16
标识
DOI:10.1016/j.jes.2022.03.044
摘要

A novel hierarchical bowl-like FeCuS@Cu2S@Fe0 nanohybrid catalyst (B-FeCuS@Cu2S@Fe0) was synthesized for removing sulfamethoxazole (SMX) through catalytic activation of peroxymonosulfate (PMS). It was found that this catalyst exhibited excellently high catalytic activity. Under optimized reaction conditions, all the added SMX (12 mg/L) could be completely degraded within 5 min. The SMX degradation followed pseudo first order kinetics with a rate constant k of 0.89 min-1, being 1.38, 4.51, 8.99 and 35.6 times greater than that of other catalysts including Fe0 (0.644 min-1 in the very initial stage), bowl-like iron-doped CuS (B-FeCuS, 0.197 min-1), bowl-like CuS (B-CuS, 0.099 min-1) and Cu2O (0.025 min-1), respectively. During the degradation, several reactive oxygen species (·OH, SO4·- and 1O2) were generated with ·OH as the main one as confirmed by electron paramagnetic resonance analysis. The SMX degradation in the present system included both radical and non-radical mediated processes. A possible mechanistic insight of the PMS activation by bowl Fe0 decorated CuS@Cu2S-based catalyst was proposed according to X-ray photoelectron spectroscopic (XPS) analysis, and the degradation pathway of SMX was speculated by monitoring the degradation intermediates with liquid chromatography coupled with mass spectrometry (LC-MS).
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