Insight into the degradation of ciprofloxacin by medium-pressure UV-activated monochloramine process

The degradation efficiency and mechanisms of ciprofloxacin (CIP), a typical antibiotic, by a medium-pressure ultraviolet/chloramine (MPUV/NH2Cl) treatment were investigated. The results showed that CIP degradation by MPUV/ NH2Cl was significantly higher than that by NH2Cl oxidation and MPUV photolysis, and that this degradation processes were consistent with pseudo-first-order kinetics. The initial CIP concentration (7.5-30.2 mu M) and the presence of HCO3- (0.5-10 mM) significantly inhibited CIP degradation with k(obs,CIP) 0.0090-0.0069 and 0.0078-0.0048 cm(2)/ mJ. In contrast, NO3- (50-500 mu M) and Br-(0.5-10 mM) significantly promoted the degradation with kobs,CIP 0.0078-0.0102 and 0.0078-0.0124 cm(2)/mJ. The effect of Cl- (0.5-10 mM) and natural organic matter (1-5 mg/L) were negligible. The NH2Cl dosage (30-60 mu M) presented a dual effect, in which its increase within the optimal concentration range (30-40 mu M) accelerated CIP degradation due to the formation of reactive radicals, whereas an excessive increase (40-60 mu M) quenched the free radicals, ultimately quenching the free radicals and inhibiting the degradation. The optimum pH for CIP degradation under MPUV/NH2Cl treatment was 7.0. The contribution of reactive halogen species (i.e., reactive chlorine species and reactive nitrogen species) to CIP degradation was substantially greater than that of hydroxyl radicals under acidic or neutral conditions. We identified the degradation products of CIP and proposed degradation pathways, which included defluorination and cracking of the piperazine ring, with the latter being dominant. Compared to haloacetic acid (HAA) and nitrogenous disinfection byproducts (N-DBPs), MPUV/ NH2Cl significantly reduced trihalomethane (THM) production and theoretical cytotoxicity by 80.1% and 78.4% respectively, compared to the background experiment in natural water at a UV dose of 300 mJ/cm(2).

Automated summary

The degradation efficiency and mechanisms of ciprofloxacin (CIP) by a medium-pressure ultraviolet/chloramine treatment were investigated. The results showed that this treatment method had significantly higher degradation efficiency compared to other methods, and the degradation process followed pseudo-first-order kinetics. The initial CIP concentration and the presence of HCO3- inhibited degradation, while NO3- and Br- promoted degradation. Cl- and natural organic matter had negligible effects on degradation. The dosage of NH2Cl had a dual effect, with an optimal concentration range accelerating degradation and excessive dosage inhibiting degradation. The optimal pH for CIP degradation was 7.0. Reactive halogen species contributed more to CIP degradation than hydroxyl radicals. Compared to background experiments, MPUV/NH2Cl treatment significantly reduced the production of trihalomethane and nitrogenous disinfection byproducts, resulting in lower theoretical cytotoxicity.