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 (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 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·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.
Keywords: Boron-doped diamond electrode; Energy consumption; Hydroxyl radical; Ofloxacin; Reactive chlorine species; Response surface methodology.
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