Photocatalytic degradation of DNOC in aqueous TiO2 dispersions -: Investigation of the initial reaction steps

被引:6
作者
Fabbri, D.
Villata, L. S.
Prevot, A. Bianco
Capparelli, A. L.
Pramauro, E.
机构
[1] Univ Turin, Dipartimento Chim Analit, I-10125 Turin, Italy
[2] Natl Univ La Plata, CONICET, Fac Ciencias Exactas, INIFTA,Dept Quim, RA-1900 La Plata, Argentina
关键词
photocatalysis; DNOC; intermediates; degradation mechanism;
D O I
10.1016/j.jphotochem.2005.10.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The photocatalytic transformation odf the pesticide 4.6-dinitro-o-cresol (DNOC) over irritated TiO2 suspensions was investigated in aerated aqueous solutions. Complete and relatively fast substrate degradation was achieved after irradiation was simulated solar light. being the reaction rate dependent on the initial pH. The slower evolution of the mineralization process, which can be accomplished after long irradiation times. was evidenced by monitering the dissolved organic carbon decrease and the formation of nitrogen inorganic products. Both the analysis of the reaction end-products and the HPLC-MC characterization of the organic intermediates are consistent with a reation mechanism where the hydroxylation of the aromatic ring and the oxidation of the methyl group can play a major role as initial reaction steps and occur at comparable rates. The direct reduction of nitro groups at the semiconductor surface to form ammonium ion, inferred from the MS analysis of minor aromatic intermediates, appears to be anopther viable reaction path. The nearly quantitative mineralization of the pesticide has been observed after long term (3h) irradiation, time after which no aromatic products were dectected. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:157 / 164
页数:8
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