Photochemical degradation study of irgarol 1051 in natural waters: influence of humic and fulvic substances on the reaction

2002 ◽  
Vol 147 (2) ◽  
pp. 135-141 ◽  
Author(s):  
Vasilios A Sakkas ◽  
Dimitra A Lambropoulou ◽  
Triantafyllos A Albanis
2005 ◽  
Vol 23 (9) ◽  
pp. 1257-1263 ◽  
Author(s):  
Li-Qin Wang ◽  
Guo-Zheng Liang ◽  
Gao-Chao Dang ◽  
Fang Wang ◽  
Xiao-Pan Fan ◽  
...  

1998 ◽  
Vol 32 (21) ◽  
pp. 3442-3447 ◽  
Author(s):  
Miguel Angel González-MartÍnez ◽  
José Penalva ◽  
Rosa Puchades ◽  
Angel Maquieira ◽  
Berta Ballesteros ◽  
...  

1998 ◽  
Vol 62 (2) ◽  
pp. 353-359 ◽  
Author(s):  
L Monney ◽  
R Belali ◽  
J Vebrel ◽  
C Dubois ◽  
A Chambaudet

Chemosphere ◽  
1994 ◽  
Vol 28 (7) ◽  
pp. 1361-1368 ◽  
Author(s):  
Marijan Ahel ◽  
Frank E. Scully ◽  
Jürg Hoigné ◽  
Walter Giger

Molecules ◽  
2021 ◽  
Vol 26 (17) ◽  
pp. 5331
Author(s):  
Cristina Jiménez-Holgado ◽  
Paola Calza ◽  
Debora Fabbri ◽  
Federica Dal Bello ◽  
Claudio Medana ◽  
...  

This study investigated the direct and indirect photochemical degradation of citalopram (CIT), a selective serotonin reuptake inhibitor (SSRI), under natural and artificial solar radiation. Experiments were conducted in a variety of different operating conditions including Milli-Q (MQ) water and natural waters (lake water and municipal WWT effluent), as well as in the presence of natural water constituents (organic matter, nitrate and bicarbonate). Results showed that indirect photolysis can be an important degradation process in the aquatic environment since citalopram photo-transformation in the natural waters was accelerated in comparison to MQ water both under natural and simulated solar irradiation. In addition, to investigate the decontamination of water from citalopram, TiO2-mediated photocatalytic degradation was carried out and the attention was given to mineralization and toxicity evaluation together with the identification of by-products. The photocatalytic process gave rise to the formation of transformation products, and 11 of them were identified by HPLC-HRMS, whereas the complete mineralization was almost achieved after 5 h of irradiation. The assessment of toxicity of the treated solutions was performed by Microtox bioassay (Vibrio fischeri) and in silico tests showing that citalopram photo-transformation involved the formation of harmful compounds.


2010 ◽  
Vol 44 (12) ◽  
pp. 4564-4569 ◽  
Author(s):  
Michela Sturini ◽  
Andrea Speltini ◽  
Federica Maraschi ◽  
Antonella Profumo ◽  
Luca Pretali ◽  
...  

2014 ◽  
Vol 11 (20) ◽  
pp. 5969-5985 ◽  
Author(s):  
J.-F. Lapierre ◽  
P. A. del Giorgio

Abstract. Despite the rapidly increasing volume of research on the biological and photochemical degradation of DOC (dissolved organic carbon) in aquatic environments, little is known of the large-scale patterns in biologically and photochemically degradable DOC (BDOC and PDOC, respectively) in continental watersheds, and on the links that exist between these two key properties that greatly influence the flow of carbon from continents to oceans. Here we explored the patterns in the concentrations and proportions of BDOC and PDOC across hundreds of boreal lakes, rivers and wetlands spanning a large range of system trophic status and terrestrial influence, and compared the drivers of these two reactive pools of DOC at the landscape level. Using standardized incubations of natural waters, we found that the concentrations of BDOC and PDOC covaried across all systems studied but were nevertheless related to different pools of dissolved organic matter (DOM; identified by fluorescence analyses) in ambient waters. Concentrations of nutrients and protein-like fluorescent DOM (FDOM) explained nearly half of the variation in BDOC, whereas PDOC was exclusively predicted by DOM optical properties, consistent with the photochemical degradability of specific FDOM pools that we experimentally determined. The concentrations of colored DOM (CDOM), which we use here as a proxy of terrestrial influence, almost entirely accounted for the observed relationship between FDOM and the concentrations of both BDOC and PDOC. The concentrations of CDOM and of the putative biolabile fluorescence component shifted from complete decoupling in clear-water environments to strong coupling in darker streams and wetlands. This suggests a baseline autochthonous BDOC pool fueled by internal production that is gradually overwhelmed by land-derived BDOC as terrestrial influence increases across landscape gradients. The importance of land as a major source of both biologically and photochemically degradable DOC for continental watersheds resulted in a partial coupling of those carbon pools in natural freshwaters, despite fundamental contrasts in terms of their composition and regulation.


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