2021
DOI: 10.1016/j.scitotenv.2020.144304
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UV/chlorine process for degradation of benzothiazole and benzotriazole in water: Efficiency, mechanism and toxicity evaluation

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Cited by 67 publications
(20 citation statements)
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“…For UV/HOCl and UV/NH 2 Cl, the peak areas of atenolol, lamotrigine, metoprolol, benzotriazole, and two methylated benzotriazoles detected in ROP were unchanged by exposure to HOCl and NH 2 Cl, indicating that these compounds were recalcitrant to rapid oxidation by low concentrations of these oxidants (Figure a,c and Figure S2a). This trend was consistent with the results of similar studies, where atenolol, metoprolol, and benzotriazole were poorly degraded by chlorination. …”
Section: Resultssupporting
confidence: 91%
“…For UV/HOCl and UV/NH 2 Cl, the peak areas of atenolol, lamotrigine, metoprolol, benzotriazole, and two methylated benzotriazoles detected in ROP were unchanged by exposure to HOCl and NH 2 Cl, indicating that these compounds were recalcitrant to rapid oxidation by low concentrations of these oxidants (Figure a,c and Figure S2a). This trend was consistent with the results of similar studies, where atenolol, metoprolol, and benzotriazole were poorly degraded by chlorination. …”
Section: Resultssupporting
confidence: 91%
“…On the other hand, the manuscripts cited and discussed in this review clearly showed that heterocyclic compounds play an essential role in controlling a phytopathogen such as FOX , being benzothiazole derivatives, the most studied compounds with the highest antifungal activity ( Table 1 ). Some reports have described biological and environmental effects and their potential activity, degradation pathways, and subproducts characterization of synthetic heterocycles such as podophyllotoxin derivatives [ 148 ], rhodamine derivatives and analogs [ 149 ], benzothiazole and benzotriazole derivatives—which have emerged as contaminants in aquatic environments and toxic to aquatic organisms [ 150 , 151 , 152 , 153 ]—and polycyclic (hetero)aromatic hydrocarbons compounds which recently was demonstrated their predominance in contaminated food samples and their relationship with potential toxicity [ 154 ]. However, further studies are necessary to establish these promissory antifungal agents’ potential cytotoxicity and environmental risks.…”
Section: Discussionmentioning
confidence: 99%
“…The explanation for this phenomenon involves the reactions between Cl − and •OH to form •ClOH − [39]. In addition, Cl − can react with •Cl to produce •Cl2 − [40]. The produced •ClOH − and •Cl2 − can be decomposed into •OH and •Cl in a reversible manner [41].…”
Section: Effects Of Inorganic Ions On Iopromide Degradation By Uv/chl...mentioning
confidence: 99%