Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10372751 | Journal of Hazardous Materials | 2011 | 7 Pages |
Abstract
Within the context of environmentally friendly methods for the elimination of surface-water pollutants, the photodegradation of the phenolic pesticides bromoxynil (BXN) and dichlorophen (DCP) under simulated natural conditions has been studied. The work was done in the presence of the visible-light absorber photosensitizer riboflavin (Rf), usually present in trace quantities in natural waters. Under aerobic conditions, an efficient photooxidation of both pesticides was observed. The relatively intricate photochemical mechanism involves pesticide and oxygen consumption and, to a lesser extent, Rf degradation. The kinetic and mechanistic study supports that both H2O2 and singlet molecular oxygen, O2(1Îg), are involved in the process. Kinetic data for the O2(1Îg)-mediated oxidation indicate that BXN and DCP are photodegraded with this species faster than the parent compound phenol, very frequently employed as a model for aquatic contaminants, likely due to their lower pKa values. This observation allows the design of phenolic pesticides with different photodegradation rates under environmental conditions.
Related Topics
Physical Sciences and Engineering
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Authors
Juan P. Escalada, Adriana Pajares, José Gianotti, Alicia Biasutti, Susana Criado, Patricia Molina, Walter Massad, Francisco Amat-Guerri, Norman A. GarcÃa,