Indirect photodegradation is one of the primary approaches for the removal of pharmaceutical contaminants from water. This degradation process is dominated by chromophoric dissolved organic matter (CDOM). After illumination, CDOM produces many reactive intermediates, which can react with drug pollutants to achieve indirect photodegradation. In this article, we focused on four different sources of CDOM and factors affecting indirect sulfamethoxazole (SMZ) photolysis. The results show that the indirect photodegradation effect of SMZ is significantly influenced by CDOM. This indirect photodegradation has a dual nature. It promotes the indirect photodegradation of SMZ through the formation of various reactive intermediates and at the same time inhibits the photodegradation of SMZ through light shielding and masking of reactive intermediates. The indirect photodegradation of SMZ is mainly controlled by active intermediates such as CDOM, HO·, and O produced by CDOM; CDOM is the main participant in indirect photodegradation of SMZ. In addition, the pH, salinity, and nitrate ions have a significant effect on the indirect photodegradation of SMZ, while bicarbonate ions have no significant effect on the indirect photodegradation of SMZ.
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http://dx.doi.org/10.13227/j.hjkx.201805014 | DOI Listing |
Chemosphere
February 2025
Département des sciences de la Terre et de l'atmosphère, Université du Québec à Montréal, Montréal, QC, H2X 1Y4, Canada; Geotop Research Centre, Montréal, QC, H2X 3Y7, Canada. Electronic address:
Many processes can contribute to the attenuation of the frequently detected and toxic herbicides atrazine and metolachlor in surface water, including photodegradation. Multi-element compound-specific isotope analysis has the potential to decipher between these different degradation pathways as Cl is a promising tool for both pathway identification and a sensitive indicator of degradation for both atrazine and metolachlor. In this study, photodegradation experiments of atrazine and metolachlor were conducted under simulated sunlight in buffered solutions (direct photodegradation) and with nitrate (indirect photodegradation by OH radicals) to determine kinetics, transformation products and isotope fractionation for C, N and for the first time Cl.
View Article and Find Full Text PDFWater Res
December 2024
Fujian Key Laboratory of Coastal Pollution Prevention and Control, College of the Environment & Ecology, Xiamen University, Xiamen 361102, China. Electronic address:
Halogenated bisphenol compounds are prevalent in urban water systems and may pose greater environmental risks than their bisphenol precursors. This study explored the formation of halogenated bisphenol F (BPF) in water chlorination and their subsequent transformation behaviors in receiving waters. The kinetics and pathways of BPF halogenation with chlorine, bromine, and iodine were firstly investigated.
View Article and Find Full Text PDFWater Res
March 2025
Dipartimento di Chimica, Università di Torino, Torino, Italy.
Sci Total Environ
December 2024
Department of Civil Engineering, Lassonde School of Engineering, York University, Toronto, Ontario, Canada. Electronic address:
J Hazard Mater
November 2024
State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Science, Chinese Academy of Sciences, Beijing 100085, China; School of Environment, Hangzhou Institute for Advanced Study, UCAS, Hangzhou 330106, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Based on sampling from Xiaoqing River of China and elimination experiments, this study first investigated spatial/seasonal profiles and fates of phenylmethylsiloxanes (PMSs), as modified products of dimethylsiloxanes (DMSs), in natural waterbody. Overall, the average water (6.7 ng/L) and sediment (28.
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