Degradation of flumequine in aqueous solution by persulfate activated with common methods and polyhydroquinone-coated magnetite/multi-walled carbon nanotubes catalysts

过硫酸盐 催化作用 化学 水溶液 激进的 氟甲喹 脱碳 羟基自由基 降级(电信) 分解 多相催化 碳纳米管 活性炭 磁铁矿 无机化学 核化学 光化学 材料科学 有机化学 矿物学 纳米技术 恩诺沙星 赤铁矿 吸附 抗生素 生物化学 环丙沙星 计算机科学 电信
作者
Mingbao Feng,Ruijuan Qu,Xiaoling Zhang,Ping Sun,Yunxia Sui,Liansheng Wang,Zunyao Wang
出处
期刊:Water Research [Elsevier]
卷期号:85: 1-10 被引量:235
标识
DOI:10.1016/j.watres.2015.08.011
摘要

In recent years, flumequine (FLU) has been ubiquitously detected in surface waters and municipal wastewaters. In light of its potential negative impacts to aquatic species, growing concern has been arisen for the removal of this antibiotic from natural waters. In this study, the kinetics, degradation mechanisms and pathways of aqueous FLU by persulfate (PS) oxidation were systematically determined. Three common activation methods, including heat, Fe2+ and Cu2+, and a novel heterogeneous catalyst, namely, polyhydroquinone-coated magnetite/multi-walled carbon nanotubes (Fe3O4/MWCNTs/PHQ), were investigated to activate PS for FLU removal. It was found that these three common activators enhanced FLU degradation obviously, while several influencing factors, such as solution pH, inorganic ions (especially HCO3− at 5 mmol/L) and dissolved organic matter extracts, exerted their different effects on FLU removal. The catalysts were characterized, and an efficient catalytic degradation performance, high stability and excellent reusability were observed. The measured total organic carbon levels suggested that FLU can be effectively mineralized by using the catalysts. Radical mechanism was studied by combination of the quenching tests and electron paramagnetic resonance analysis. It was assumed that sulfate radicals predominated in the activation of PS with Fe3O4/MWCNTs/PHQ for FLU removal, while hydroxyl radicals also contributed to the catalytic oxidation process. In addition, a total of fifteen reaction intermediates of FLU were identified, from which two possible pathways were proposed involving hydroxylation, decarbonylation and ring opening. Overall, this study represented a systematical evaluation regarding the transformation process of FLU by PS, and showed that the heterogeneous catalysts can efficiently activate PS for FLU removal from the water environment.
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