Enhanced electron transfer for activation of peroxymonosulfate via MoS2 modified iron-based perovskite

电子顺磁共振 催化作用 钙钛矿(结构) 化学 X射线光电子能谱 降级(电信) 电子转移 无机化学 可重用性 光化学 化学工程 有机化学 电信 物理 软件 计算机科学 工程类 程序设计语言 核磁共振
作者
Sheng Sheng,Jingjing Fu,Siwei Song,Yan‐Bing He,Jin Qian,Ziyang Yi
出处
期刊:Environmental Technology [Informa]
卷期号:: 1-17 被引量:1
标识
DOI:10.1080/09593330.2022.2137438
摘要

The increasing use of fluoroquinolone antibiotics, which are found in various environmental media, is a constant threat to ecological safety and human health. In this paper, SrFeO3@MoS2 heterogeneous catalyst was prepared to activate peroxymonosulfate (PMS) for the degradation of levofloxacin (LVO). The characteristics of SrFeO3@MoS2 samples were studied and the optimum conditions for the removal of LVO by SrFeO3@MoS2/PMS system were investigated. The removal of LVO by the SrFeO3@MoS2-0.3/PMS system could reach 96.06% within 20 min of reaction. The effect of inorganic anions (SO42-, Cl-, NO3- and H2PO4-) commonly found in actual water bodies on catalytic reaction was explored. The reusability investigation revealed that the catalyst could still remove 88.06% of LVO within 20 min after four cycles. Moreover, SO4•-, •OH and 1O2 were identified by Electron Paramagnetic Resonance (EPR) tests and scavenger experiments, where the SO4•- and •OH were dominant reactive species. Combining with the XPS characterisation, the activation mechanism of SrFeO3@MoS2-0.3/PMS was proposed, and the oxygen vacancies and transition metals on the sample surface were active sites of PMS activation. Furthermore, the possible degradation pathways of LVO were well-established based on the detected intermediates.
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