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电化学驱动 UV/氯工艺去除分散式水处理中的抗生素耐药菌和抗生素耐药基因。

Removal of antibiotic resistant bacteria and antibiotic resistance genes by an electrochemically driven UV/chlorine process for decentralized water treatment.

机构信息

State of Key Laboratory of Natural Medicines, School of Engineering, China Pharmaceutical University, Nanjing 211198, China; School of Environment, Beijing Key Laboratory for Emerging Organic Contaminants Control, State Key Joint Laboratory of Environmental Simulation and Pollution Control, Tsinghua University, Beijing 100084, China.

State of Key Laboratory of Natural Medicines, School of Engineering, China Pharmaceutical University, Nanjing 211198, China.

出版信息

Water Res. 2024 Nov 1;265:122298. doi: 10.1016/j.watres.2024.122298. Epub 2024 Aug 17.

Abstract

The UV/chlorine (UV/Cl) process is a developing advanced oxidation process and can efficiently remove antibiotic resistant bacteria (ARB) and antibiotic resistance genes (ARGs). However, the transportation and storage of chlorine solutions limit the application of the UV/Cl process, especially for decentralized water treatment. To overcome the limitation, an electrochemically driven UV/Cl process (E-UV/Cl) where Cl can be electrochemically produced in situ from anodic oxidation of chloride (Cl) ubiquitously present in various water matrices was evaluated in this study. >5-log inactivation of the ARB (E. coli) was achieved within 5 s of the E-UV/Cl process, and no photoreactivation of the ARB was observed after the treatment. In addition to the ARB, intracellular and extracellular ARGs (tetA, sul1, sul2, and ermB) could be effectively degraded (e.g., log(C/C) > 4 for i-ARGs) within 5 min of the E-UV/Cl process. Atomic force microscopy showed that the most of the i-ARGs were interrupted into short fragments (< 30 nm) during the E-UV/Cl process, which can thus effectively prevent the self-repair of i-ARGs and the horizontal gene transfer. Modelling results showed that the abatement efficiencies of i-ARG correlated positively with the exposures of •OH, Cl•, and ClO• during the E-UV/Cl process. Due to the short treatment time (5 min) required for ARB and ARG removal, insignificant concentrations of trihalomethanes (THMs) were generated during of the E-UV/Cl process, and the energy consumption (E) of ARG removal was ∼0.20‒0.27 kWh/m-log, which is generally comparable to that of the UV/Cl process (0.18-0.23 kWh/m-log). These results demonstrate that the E-UV/Cl process can provide a feasible and attractive alternative to the UV/Cl process for ARB and ARG removal in decentralized water treatment system.

摘要

紫外线/氯(UV/Cl)工艺是一种正在发展的高级氧化工艺,可有效去除抗生素耐药菌(ARB)和抗生素耐药基因(ARGs)。然而,氯溶液的运输和储存限制了 UV/Cl 工艺的应用,尤其是在分散式水处理中。为了克服这一限制,本研究评估了一种电化学驱动的 UV/Cl 工艺(E-UV/Cl),该工艺可通过阳极氧化普遍存在于各种水基质中的氯离子(Cl)原位电化学产生 Cl。在 E-UV/Cl 工艺中,5 秒内可使 ARB(大肠杆菌)灭活超过 5 个对数,处理后未观察到 ARB 的光复活。除了 ARB 之外,细胞内和细胞外的 ARGs(tetA、sul1、sul2 和 ermB)也可在 5 分钟内有效降解(例如,i-ARGs 的 log(C/C) > 4)。原子力显微镜显示,在 E-UV/Cl 工艺过程中,大多数 i-ARGs 被打断成短片段(<30nm),从而可以有效地阻止 i-ARGs 的自我修复和水平基因转移。模型结果表明,i-ARG 的去除效率与 E-UV/Cl 工艺过程中•OH、Cl•和 ClO•的暴露量呈正相关。由于去除 ARB 和 ARG 所需的处理时间(5 分钟)很短,因此在 E-UV/Cl 工艺过程中不会产生显著浓度的三卤甲烷(THMs),而去除 ARG 的能量消耗(E)约为 0.20-0.27 kWh/m-log,与 UV/Cl 工艺(0.18-0.23 kWh/m-log)相当。这些结果表明,E-UV/Cl 工艺可为分散式水处理系统中 ARB 和 ARG 的去除提供一种可行且有吸引力的替代 UV/Cl 工艺的方法。

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