Photodegradation of phenylurea herbicides sensitized by norfloxacin and the influence of natural organic matter.

The photochemical activity of fluoroquinolone antibiotics (FQs) has gained attention due to the discovery of their phototoxicity and photocarcinogenicity in clinics. This study reveals that norfloxacin (NOR) can sensitize the photodegradation of phenylurea (PU) herbicides. This is attributed to the formation of an excited triplet of norfloxacin (NOR*) by UV-A irradiation of its quinolone chromophore, which can further react with O to form singlet oxygen (O). The second-order rate of NOR* with PU ranges from 1.54 × 10 to 2.76 × 10 Ms. The steady-state concentrations of NOR* were calculated as (4.29-31.2)× 10 M at 10 μM NOR under UV irradiation. Natural organic matter (NOM) inhibited the degradation of PU induced by NOR*. In the presence of 10 mg L NOM, the pseudo-first-order rate constants (k) of the degradation of diuron (DIU), isoproturon (IPU), monuron (MOU), and chlorotoluron (CLU) decreased by 65%, 19%, 36%, and 62%, respectively. NOM mainly acts as a reductant which reacted with the radical intermediates of the PU generated by NOR*oxidation, thus reversing the oxidation. The inhibitory effect increases with increasing NOM concentration. Results of this study underscore the role of NOR as a photosensitizer in accelerating the abatement of PU pesticides in sunlit surface waters. This study significantly advances the understandings of the behavior of NOR in aquatic environments.