The photocatalytic degradation of selected s-triazine herbicides and organophosphorus insecticides was carried out in aqueous TiO2 suspensions under simulated solar light. The tested herbicides from the s-triazines group were atrazine, propazine, cyanazine, prometryne, and irgarol. The tested insecticides from the organophosphorus group were ethyl parathion, methyl parathion, ethyl bromophos, methyl bromophos, and diclofenthion. Degradation kinetics followed first-order reaction and has been monitored through gas chromatography. The degradation was fast with half-lives varying from 10.2 to 38.3 min depending on the nature and the structure of compounds. The generated transformation products (TPs) were formed via oxidation, dealkylation, and dechlorination for s-triazines and via oxidation and photohydrolysis for organophosphates. The TPs of irgarol, bromophos, and dichlofenthion were identified using solid-phase extraction (SDB-disks) and GC-MS techniques, and possible degradation routes were proposed showing similar degradation pathways as for other triazines and organophosporus pesticides. This work points out to the necessity of extended knowledge of the successive steps in a solar-assisted detoxification process.
To elucidate the photochemical behavior of pesticide metolachlor, degradation was carried out in aqueous media of different compositions such as sea, river, lake, and distilled water under natural and simulated solar irradiation. In addition, the effect of important constituents of natural water such as dissolved organic matter (DOM, isolated from Pamvotis Lake) and nitrate ions was also examined. It was found that photodegradation proceeds via a pseudo-first-order reaction in all cases. The presence of DOM inhibits the photolysis reaction with half-lives ranging from 87 to 693 h whereas the degradation rate was accelerated up to 11 times in the presence of NO(3)(-). In addition, the toxicity of the degradation products formed (generally through hydroxylation, dealkylation, and cyclization reactions) was also performed using the marine luminescent bacterium Vibrio fisheri. Our results indicated a toxicity increase of the irradiated solution showing that photoproducts of higher acute toxic effects were formed.
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