Abstract
It is important to study the fate and transport of antibiotics in aquatic environments to reveal their pollution status. The premise behind fate and transport studies is to evaluate the reaction processes of the target antibiotics. However, available research on the environmental behaviors of antibiotics in certain natural waters, such as estuarine water, is scarce. In this study, single reactions such as sorption, biodegradation, and photolysis and multiple degradation reactions of sulfamethoxazole (SMX), trimethoprim (TMP), and ciprofloxacin (CIP) in the estuarine water were studied. The sorption rates of the target antibiotics in the estuarine water-sediment system were very fast, and the sorption amounts varied among sediments and antibiotics. Hydrolysis did not contribute to the degradation of the target antibiotics. Biodegradation had a low contribution to the degradation of the target antibiotics in the estuarine water. In comparison, photolysis was the dominant degradation process for SMX, TMP, and CIP. The rates of photolysis of the tested antibiotics in the estuarine water were greater than those in pure water; thereby, indicating photolysis of these antibiotics was more prone to occur in the estuarine water. In the multiple degradation experiments, it was found that there may be synergistic effects between the single degradation processes. Thus, the aqueous concentrations of antibiotics decreased rapidly by sorption after entering the estuarine water and then decreased relatively slowly by photolysis and biodegradation. This study provides information for evaluating the environmental behaviors of antibiotics in estuarine environments.
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Funding
This study was financially supported by Shandong Key Laboratory of Coastal Environmental Processes, YICCAS (2019SDHADKFJJ12), and the Natural Science Foundation of the Jiangsu Higher Education Institutions of China (19KJB610007).
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Li, J., Cui, M. Kinetic study on the sorption and degradation of antibiotics in the estuarine water: an evaluation based on single and multiple reactions. Environ Sci Pollut Res 27, 42104–42114 (2020). https://doi.org/10.1007/s11356-020-10194-4
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DOI: https://doi.org/10.1007/s11356-020-10194-4