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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 ⩽ 1 mg C L(-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<6.5, for cefapirin as well. In contrast, direct photolysis would be negligible for cefradine and cefalexin. The DOC values would influence the fraction of photodegradation accounted for by direct photolysis in shallow water, to a different extent depending on the role of sensitisation by the triplet states of chromophoric dissolved organic matter.
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http://dx.doi.org/10.1016/j.chemosphere.2015.04.102 | DOI Listing |
J Hazard Mater
August 2025
State Key Laboratory of Water Pollution Control and Green Resource Recycling, School of the Environment, Nanjing University, Nanjing, China; Institute for the Environment and Health, Nanjing University Suzhou Campus, Suzhou, China. Electronic address:
The in-situ utilization of dissolved organic matter (DOM) for photosensitized activation of chemical oxidants towards micropollutant abatement presents a promising strategy aligned with the UN's Sustainable Development Goals. This study investigates the degradation of micropollutants via DOM-mediated photosensitized activation of peracetic acid (PAA) under solar irradiation and elucidates the underlying mechanisms. In wastewater effluent containing 5 mg/L DOM and 83 μM PAA, sunlight exposure facilitated DOM-mediated PAA activation, increasing the concentration of oxidative reactive species (ORS) by 50 % compared to DOM-free conditions.
View Article and Find Full Text PDFPhys Chem Chem Phys
August 2025
Max-Planck-Institute for Chemistry, Division of Atmospheric Chemistry, 55128 Mainz, Germany.
Trifluoroacetaldehyde (CFCHO) is formed in the atmosphere by the oxidation of a number of fluorinated, organic compounds of anthropogenic origin. The reaction of CFCHO with the OH radical is a potential source of atmospheric trifluoroacetic acid (TFA) which is a highly persistent, water-soluble compound that may accumulate in aquatic ecosystems and for which uncertainty about its sources, fate, and potential ecological impact persists. In light of growing concerns about the impact of TFA, we present the first study of the temperature dependence of the rate coefficient for the title reaction over the atmospherically relevant temperature range of 204 K to 361 K.
View Article and Find Full Text PDFJ Am Chem Soc
August 2025
Department of Chemistry and Biochemistry, University of California Los Angeles, Los Angeles, California 90095, United States.
Ni-catalyzed cross-coupling is a powerful strategy to forge C(sp)-C(sp) bonds. Typically, to do so requires overcoming a challenging C-C bond-forming reductive elimination, often enabled by the intermediacy of highly oxidized Ni species or outer-sphere processes. While direct C(sp)-C(sp) reductive elimination from the Ni base oxidation state is normally thermally inaccessible, light-activation provides an avenue to affect such transformations.
View Article and Find Full Text PDFEnviron Sci Process Impacts
August 2025
College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing 210095, China.
Ambroxol (AMB), a widely used expectorant drug, has been ubiquitously detected in aquatic environments due to its limited metabolism in the human body. Herein, we systematically investigated the photodegradation of AMB in waters upon natural sunlight irradiation. AMB has a p value of 8.
View Article and Find Full Text PDFJ Hazard Mater
August 2025
University of Maryland Baltimore County, Department of Chemical, Biochemical, and Environmental Engineering, 1000 Hilltop Circle, Engineering 314, Baltimore, MD 21250, USA. Electronic address:
Triphenyltin hydroxide (TPTH) is an organotin fungicide that causes endocrine disruption and reproductive malformation in aquatic organisms. The objectives of this study were to determine the photodegradation kinetics, identify the transformation products, and measure the residual toxicity of TPTH during UV-254 and UV-HO treatment. The quantum yield of TPTH was 0.
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