4.8 Article

Activation of hydrogen peroxide, persulfate, and free chlorine by steel anode for treatment of municipal and livestock wastewater: Unravelling the role of oxidants speciation

期刊

WATER RESEARCH
卷 216, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2022.118305

关键词

Electrochemical advanced oxidation processes; Micropollutants; Transformation products; Oxidants

资金

  1. National Research Foundation of Korea (NRF) - Korean government (MSIP) [NRF-2017R1A2B3012681]
  2. Ministry of Trade, Industry & Energy (MOTIE, Korea) under Materials/Components Technology Development Program [20011360]
  3. Korea Evaluation Institute of Industrial Technology (KEIT) [20011360] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

In this study, electrochemical activation of hydrogen peroxide, persulfate, and free chlorine was used for industrial-scale treatment of municipal and livestock wastewater, focusing on micropollutants and transformation products. Optimized conditions were determined for each treatment, and the speciation of oxidants was analyzed to understand their effects on treatment efficiency and by-product formation.
Despite the extensive application of electrochemical advanced oxidation processes (EAOPs) in wastewater treatment, the exact speciation of oxidants and their effects on pollutants removal efficiency, by-products formation, and effluent toxicity are largely unknown. In this study, galvanostatic steel anodes were used to drive the electrochemical activation of hydrogen peroxide (EAHP), persulfate (EAP), and free chlorine (EAFC), for industrial-scale treatment of municipal and livestock wastewater with a focus on micropollutants and transformation products (MTPs) and effluent toxicity. Response surface methodology determined the optimized conditions for each treatment towards total organic carbon ([TOC](0) = 180 mg/L) removal at pH 3.0: persulfate dose = 0.12 mmol/min, 26.5 mA/cm(2); free chlorine dose = 0.29 mmol/min, 37.4 mA/cm(2); H2O2 dose = 0.20 mmol/min, 45 mA/cm(2). Probe-compound degradation revealed that HO center dot, SO4(center dot-) and (FeO2+)-O-IV species were simultaneously generated in EAP, whereas HO center dot and (FeO2+)-O-IV were the principal oxidants in EAHP and EAFC, respectively. Samples were analyzed via liquid and gas chromatography in non-target screening (NTS) mode to monitor the generation or removal of MTPs and by-products including compounds that have not been reported previously. The speciation of oxidants, shifted in presence of halide ions (Cl-, Br-) in real wastewater samples, significantly affected the mineralization efficiency and by-product formation. The production of halogenated byproducts in EAFC and EAP substantially increased the effluent toxicity, whereas EAHP provided non-toxic effluent and the highest mineralization efficiency (75 - 80%) to be nominated as the best strategy.

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