Journal
WATER RESEARCH
Volume 171, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2019.115374
Keywords
Sulfonamides; substituents; Nonradical oxidation; Persulfate; DFT calculation; Pathways
Funding
- China Postdoctoral Science Foundation [55350333]
- National Natural Science Foundation of China [51678188, 21577142]
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The large consumption and discharge of sulfonamides (SAs) have potentially induced antibiotic resistance genes, posing inestimable threats to humans and ecosystems. In the present study, five SAs with different substituents were regarded as target compounds to be degraded using the nonradical dominated peroxydisulfate (PDS) activation process by the combination of O-1(2) oxidation and direct electron transfer. The degradation rates, toxicities and pathways of SAs largely varied with their substituents. For instance, sulfathiazole with five-membered substituent had the highest degradation rate of 0.19 min(-1), which was 3.8 times as the rate of sulfanilamide (0.05 min(-1)) without substituent. Then the theoretical calculation was adopted to further confirm that different substituents on the SAs could influence the molecular orbital distribution and their stability, thus resulting in the different removal rate of SAs. Finally, the products of different SAs were concisely deduced to take insight into the effects of different substituents on SAs degradation pathways. It was demonstrated that the geometrical differences among various SAs caused by the different substituents contributed to the different degradation pathways of SAs. Representatively, the special Smiles-type rearrangement pathway was occurred in the six-membered SAs instead of in the five-membered SAs, which inversely resulted in the slower degradation rate of six-membered SAs than the five-membered SAs. Thus, the present study provides a valuable insight into the effects of substituents on the degradation rate and transformation pathways of SAs in the nonradical PDS activation process. (C) 2019 Published by Elsevier Ltd.
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