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Efficient degradation of methabenzthiazuron photoinduced by decatungstate anion in water: kinetics and mechanistic studies.

Chemosphere (2011-07-16)
A Allaoui, M A Malouki, P Wong-Wah-Chung
RESUMEN

This study concerns the elimination of methabenzthiazuron (MBTU) photocatalysed by sodium decatungstate salts W10O32(4-)·(DTA) in aqueous solution under irradiation at 365 nm. Ninety percentage of MBTU (10(-4) M) is mineralised in the presence of the photocatalyst (2×10(-4) M) after 7 d under exposure and the formation of nitrate, sulphate and ammonium confirmed this phenomenon. In aerated conditions, the photodegradation rate of MBTU clearly increased in the presence of DTA by a factor of 40 when compared to direct photolysis with ΦMBTU=2.5×10(-2) and t1/2 (MBTU)=1.4 h. Oxygen appeared essential since 2 times inhibition of MBTU disappearance and the photocatalytic cycle interrupt were observed in the absence of oxygen. The degradation mechanism has been elucidated through the photoproducts identification by LC-ESI-MS analysis. Two processes were implied in the degradation: electron transfer and H atom abstraction reactions both involving W10O32(4-∗) excited state species. In the primary steps of the degradation, the aromatic ring hydroxylation was observed by electron transfer leading to OH-MBTU isomers and H atom abstraction reaction gave benzthiazuron and a supposed demethylated product. Secondary oxidations permitted the hydroxylation of both products.

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Sigma-Aldrich
Sodium tungstate dihydrate, ACS reagent, ≥99%
Sigma-Aldrich
Sodium tungstate dihydrate, BioUltra, ≥99.0% (T)
Sigma-Aldrich
Sodium tungstate dihydrate, 99.995% trace metals basis
Sigma-Aldrich
Sodium tungstate dihydrate, JIS special grade, 99.0-100.5