Degradation intermediates and reaction pathway of carbofuran in leaching water using TiO2 and ZnO as photocatalyst under natural sunlight

被引:41
|
作者
Fenoll, Jose [1 ]
Hellin, Pilar [1 ]
Flores, Pilar [1 ]
Martinez, Carmen M. [1 ]
Navarro, Simon [2 ]
机构
[1] Inst Murciano Invest & Desarrollo Agr & Alimentar, Equipo Calidad Alimentaria, Murcia 30150, Spain
[2] Univ Murcia, Dept Quim Agr Geol & Edafol, Fac Quim, E-30100 Murcia, Spain
关键词
Water remediation; Carbofuran; Photocatalytic oxidation; Semiconductor materials; SEMICONDUCTOR OXIDES; AQUEOUS-SOLUTION; SENSITIZED PHOTODEGRADATION; SOLAR PHOTOCATALYSIS; IRRADIATION; PESTICIDES; PARAMETERS; HERBICIDES; OXIDATION; NITRATE;
D O I
10.1016/j.jphotochem.2012.10.012
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
In this work the solar-photocatalytical degradation of carbofuran in leaching water has been studied using zinc oxide (ZnO) and different mixed-phase (rutile/anatase) titanium dioxide (TiO2) at pilot plant scale. Comparison of catalysts showed that ZnO is the most efficient for catalyzing the removal of carbofuran and their main organic intermediates. The residual levels of carbofuran at the end of the experiment (240 min) were 0.1, 22.4, 62.8, 68.4 mu g L-1 for ZnO, TiO2 P25 Degussa (70A/30R), TiO2 rutile (25A/75R) and TiO2 anatase (90A/10R), respectively. The primary degradation of carbofuran followed pseudo-first order kinetics. The analysis and evolution of the intermediates suggest that oxidation of the C-O bond on the carbamate group and 3C position of the furan ring as the main metabolic pathway. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:33 / 40
页数:8
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