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A model assessment of the importance of direct photolysis in the photo-fate of cephalosporins in surface waters: Possible formation of toxic intermediates
[Display omitted] •Cephalosporins are transformed in surface waters by hydrolysis and photochemistry.•Photochemistry would prevail in waters with low depth and/or low DOC.•Important direct photolysis for cefazolin, negligible for cefradine and cefalexin.•Direct photolysis is favoured in shallow wate...
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Published in: | Chemosphere (Oxford) 2015-09, Vol.134, p.452-458 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Cephalosporins are transformed in surface waters by hydrolysis and photochemistry.•Photochemistry would prevail in waters with low depth and/or low DOC.•Important direct photolysis for cefazolin, negligible for cefradine and cefalexin.•Direct photolysis is favoured in shallow waters with intermediate/high DOC values.•Such conditions favour the formation of toxic intermediates.
The direct and indirect photodegradation of six cephalosporins was predicted using a photochemical model, on the basis of literature values of photochemical reactivity. Environmental photodegradation would be important in surface water bodies with depth ⩽2–3m, and/or in deeper waters with low values of the dissolved organic carbon (DOC⩽1mgCL−1). The half-life times would range from a few days to a couple of weeks in summertime. In deeper and higher-DOC waters and/or in different seasons, hydrolysis could prevail over photodegradation. The direct photolysis of cephalosporins is environmentally concerning because it is known to produce toxic intermediates. It would be a major pathway for cefazolin, an important one for amoxicillin and cefotaxime and, at pH |
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ISSN: | 0045-6535 1879-1298 |
DOI: | 10.1016/j.chemosphere.2015.04.102 |