Pesticide by-products in the Rhone delta (Southern France). The case of 4-chloro-2-methylphenol and of its nitroderivative

被引:61
作者
Chiron, Serge [1 ]
Comoretto, Laetitia [1 ]
Rinaldi, Elisabetta [2 ]
Maurino, Valter [2 ]
Minero, Claudio [2 ]
Vione, Davide [2 ]
机构
[1] Aix Marseille Univ, CNRS, UMR 6264, Lab Chim Prov, F-13331 Marseille 3, France
[2] Univ Turin, Dipartimento Chim Analit, I-10125 Turin, Italy
关键词
Environmental photochemistry; Genotoxic compounds; Environmental fate; Pesticide derivatives; DINITRO-O-CRESOL; MASS-SPECTROMETRY; AQUEOUS-SOLUTION; NATURAL-WATERS; IN-VITRO; OXIDATION; PHOTODEGRADATION; DEGRADATION; PHOTOLYSIS; NITRATE;
D O I
10.1016/j.chemosphere.2008.09.012
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A field monitoring campaign for pesticides and their transformation intermediates was carried out in the Rhone delta (Southern France). It was evidenced the following transformation sequence: MCPA --> 4-chloro-2-methylphenol (CMP) --> 4-chloro-2-methyl-6-nitrophenol (CMNP). Interestingly CMP disappeared about as quickly as MCPA, while CMNP was environmentally more persistent than the parent molecules. This is very relevant to the environmental risk associated with the occurrence of these compounds, because the nitration of chlorophenols reduces their acute toxicity but the nitroderivatives could have more marked long-term effects, associated with their genotoxicity. Irradiation experiments suggested that the photonitration of CMP into CMNP involves nitrogen dioxide, generated from the photolysis of nitrate and from the photooxidation of nitrite by (OH)-O-center dot. The photochemistry of Fe(III) species could also play a significant role, but its contribution is still difficult to be quantified. Another important intermediate of CMP transformation is methylnitrophenol (MNP), produced via a dechlorination/nitration pathway, with ortho-cresol as the most likely reaction intermediate. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:599 / 604
页数:6
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