Salah Rafqah

Kinetics and mechanism of the degradation of the pesticide metsulfuron methyl induced by excitation of iron(III) aqua complexes in aqueous solutions: steady state and transient absorption spectroscopy studies.

The degradation of the pesticide metsulfuron methyl induced by excitation of iron(III) aqua complexes was studied at 365 nm. The process involved the formation of hydroxyl radicals and was shown to depend on Fe(OH)(2+) concentration. The second order rate constant of the reaction of metsulfuron methyl and hydroxyl radical was evaluated by laser flash photolysis experiments to k = 3.5 x 10(9) mol(-1) L s(-1). Various products were formed. Among them 2-amino-4-methoxy-6-methyl-1,3,5-triazine, 2-(carbomethoxy) benzenesulfonamide and hydroxylated derivatives represent the major photoproducts. Compounds arising from the cleavage of the triazine moiety were also found. After prolonged irradiation, a total disappearance of metsulfuron methyl and a complete mineralization of the solution were obtained.

Photocatalysis of the Organophosphorus Fenamiphos: Insight into the Degradation Mechanism

The photocatalytic degradation of the organophosphorus fenamiphos (FN) was studied using titanium dioxide as a photocatalyst and 365 nm as an excitation wavelength. Under our experimental conditions and in aerated solutions, the irradiation in the presence of TiO2 P25 (1.0 g L−1) permitted the evaluation of the half lifetime to 9.5 minutes. Laser flash photolysis experiments showed the formation of an initial species owing to the attack of the hydroxyl radical on FN. It was identified as the adduct -FN. The second order rate constant for its formation was evaluated to moL−1 L s−1. All the products are formed via the formation of such transient intermediate. They were identified by means of HPLC/MS using electrospray in positive mode (). Two main processes are responsible for FN photocatalytic transformation: (i) hydroxylation on the aromatic structure and (ii) the scission of the C–O bond. A mechanistic scheme was proposed for the photocatalytic process of FN using titanium dioxide. An efficient mineralization was observed within 24 hours by using a suntest setup.