School of Environment and Architecture, University of Shanghai for Science and Technology, Shanghai, 200093, China.
State Key Laboratory of Pollution Control and Resource Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai, 200092, China.
Environ Sci Pollut Res Int. 2022 Mar;29(12):17866-17877. doi: 10.1007/s11356-021-17089-y. Epub 2021 Oct 21.
In this study, electrochemically activated peroxymonosulfate (EC/PMS) with a sacrificial iron electrode was used for the removal of chloramphenicol (CAP) from water. Compared to electrolysis alone, peroxymonosulfate (PMS) alone, and Fe/PMS, EC/PMS significantly enhanced the CAP degradation. Various parameters, such as the applied current, electrolyte concentration, and PMS dose, were investigated to optimize the process. In addition, acidic conditions facilitated the CAP degradation. The presence of Cl slightly enhanced the CAP degradation, while both HCO and NO exhibited an inhibitory effect on the CAP degradation. The floccules were also analyzed after the reaction by XPS and XRD. Quenching experiments indicated that both sulfate radicals (SO) and hydroxyl radicals (•OH) were responsible for the CAP degradation. In addition, the degradation products were identified by LC/TOF/MS, and the degradation pathways were proposed accordingly. These results indicated that EC/PMS is a promising treatment process for the remediation of water polluted by CAP.
在这项研究中,采用牺牲铁电极电化学激活过一硫酸盐(EC/PMS)来去除水中的氯霉素(CAP)。与单独电解、单独过一硫酸盐(PMS)和 Fe/PMS 相比,EC/PMS 显著增强了 CAP 的降解。研究了各种参数,如施加电流、电解质浓度和 PMS 剂量,以优化该过程。此外,酸性条件有利于 CAP 的降解。Cl 的存在略微增强了 CAP 的降解,而 HCO 和 NO 对 CAP 的降解均表现出抑制作用。反应后通过 XPS 和 XRD 对絮体进行了分析。猝灭实验表明,硫酸盐自由基(SO)和羟基自由基(•OH)都对 CAP 的降解起作用。此外,通过 LC/TOF/MS 鉴定了降解产物,并据此提出了降解途径。这些结果表明,EC/PMS 是一种有前途的处理 CAP 污染水的方法。