共 12 条
Efficient degradation of methabenzthiazuron photoinduced by decatungstate anion in water: Kinetics and mechanistic studies
被引:12
|作者:
Allaoui, A.
[3
]
Malouki, M. A.
[3
]
Wong-Wah-Chung, P.
[1
,2
]
机构:
[1] Clermont Univ, ENSCCF, Photochim Mol & Macromol Lab, F-63000 Clermont Ferrand, France
[2] CNRS, UMR 6505, LPMM, F-63173 Aubiere, France
[3] Univ Mentouri, Lab Tech Innovantes Preservat Environm, Constantine 25000, Algeria
来源:
关键词:
Methabenzthiazuron;
Herbicide;
Decatungstate anion;
Photodegradation;
UV light;
Mineralisation;
PHOTOCATALYTIC DEGRADATION;
SOIL;
PHOTOTRANSFORMATION;
PHOTODEGRADATION;
PHOTOLYSIS;
ALKENES;
D O I:
10.1016/j.chemosphere.2011.06.071
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
This study concerns the elimination of methabenzthiazuron (MBTU) photocatalysed by sodium decatung-state salts W10O324-center dot(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 x 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 Phi(MBTU) = 2.5 x 10(-2) and t(1/2) (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 W10O324-center dot 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. (C) 2011 Elsevier Ltd. All rights reserved.
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页码:558 / 564
页数:7
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