Degradation of ofloxacin by potassium ferrate: kinetics and degradation pathways

Drug residues, including various antibiotics, are being increasingly detected in aqueous environments. Ofloxacin (OFX) is one such antibiotic that is widely used in the treatment of several bacterial infections; however, chronic exposure to this antibiotic can have adverse impacts on human health. Hence, the identification of an effective OFX degradation method is essential. Thus, in this study, the degradation performance of OFX using potassium ferrate (Fe(VI)) under the influence of different initial concentrations, pH, temperature, and common ions in water was investigated. OFX degradation by Fe(VI) was directly proportional to the concentration of Fe(VI) and temperature and inversely proportional to the pH. Among the common ions in water, Fe3+ and NH4+ could significantly promote the degradation of OFX by Fe(IV), while humic acid (HA) significantly inhibited it. Under the conditions of [Fe(VI)]:[OFX] = 15:1, T = 25celcius, and pH = 7.0, the removal efficiency of 8 mu M OFX reached more than 90% in 4 min. Seven intermediates were identified by quadrupole time-of-flight tandem ultra-performance liquid chromatography mass spectrometry (Q-TOF LC/MS), and two possible pathways for the degradation of OFX by Fe(VI) were proposed. Overall, the results suggest that advanced oxidation technology using Fe(VI) is effective for treating wastewater containing OFX.

Automated summary

This study investigated the degradation performance of ofloxacin (OFX) using potassium ferrate (Fe(VI)). It was found that the presence of Fe3+ and NH4+ significantly promoted the degradation of OFX by Fe(IV), while humic acid (HA) inhibited it. Under specific conditions, Fe(VI) efficiently degraded OFX, and two possible degradation pathways were proposed.