4.7 Article

Removal of ofloxacin from wastewater by chloride electrolyte electro-oxidation: Analysis of the role of active chlorine and operating costs

Journal

SCIENCE OF THE TOTAL ENVIRONMENT
Volume 850, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.scitotenv.2022.157963

Keywords

O floxacin; Boron -doped diamond electrode; Hydroxyl radical; Reactive chlorine species; Response surface methodology; Energy consumption

Funding

  1. National Key Research and Development Program of China [2020YFC1808301]
  2. National Natural Science Foundation of China [42107483, 41907391]
  3. Department of Education of Jilin Province [JJKH20201012KJ]
  4. Scientific Frontier and Interdisciplinary Research Project of Jilin University
  5. Innovation Training Program for Undergraduate Students of Jilin University [101832020CX249]
  6. Outstanding Youth Cultivation Plan of Jilin University
  7. Graduate Innovation Fund of Jilin University [S202110183473, 101832020CX245]

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This study investigates the degradation mechanism of ofloxacin (OFX) removal through electro-oxidation (EO) and evaluates the biological toxicities of the intermediates. After optimizing the operating parameters, OFX is almost completely degraded with high energy efficiency. The proposed method emerges as a viable treatment scheme for similar polluted wastewaters.
Electro-oxidation (EO) has received increasing attention as an efficient and green method for removing pollutants from wastewater. Chloride anions (Cl-), which commonly exist in wastewater, can act as an electrolyte for the EO process. However, the role of reactive chlorine species (RCS) generated near electrodes is often underestimated. In this study, we generated hydroxyl radicals (center dot OH) and RCS in a boron-doped diamond (BDD) electrode system and investigated its degradation mechanism for ofloxacin (OFX) removal. The findings suggested that OFX degradation was dominated by center dot OH existing near the anode in solution, with RCS playing a supporting role. Based on the produced intermediates, we proposed an OFX decomposition pathway. The biological toxicities of the intermediates were evaluated through the ECOSAR and T.E.S.T. procedure. Nearly half of the intermediates are less toxic than the parent compound. After optimizing the operating parameters by the response surface methodology, 20 mg/L OFX was almost completely degraded after 10 min of reaction in 1.45 g/L NaCl with a current density (j) of 18 mA/cm2, and the total organic carbon was decreased by 30.55 %. The energy consumption and current efficiency were 0.648 kW center dot h/gTOC and 8.65 %, respectively. Comparing the operating costs of the proposed and other EO methods, our method emerged as a viable new treatment scheme for similar polluted wastewaters. This study aims to comprehensively understand the potential application value of BDD electrodes in the treatment of Cl-containing organic wastewater.

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