Babita Sur, Elisa De Laurentiis, Marco Minella, Valter Maurino, Claudio Minero, Davide Vione, Babita Sur, Elisa De Laurentiis, Marco Minella, Valter Maurino, Claudio Minero, Davide Vione
Index: Sci. Total Environ. 426 , 296-303, (2012)
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Anionic 2-nitro-4-chlorophenol (NCP) may occur in surface waters as a nitroderivative of 4-chlorophenol, which is a transformation intermediate of the herbicide dichlorprop. Here we show that NCP would undergo efficient photochemical transformation in environmental waters, mainly by direct photolysis and reaction with OH. NCP has a polychromatic photolysis quantum yield ΦNCP=(1.27±0.22)·10−5, a rate constant with OH kNCP,OH=(1.09±0.09)·1010M−1s−1, a rate constant with 1O2kNCP,1O2=(2.15±0.38)·107M−1s−1, a rate constant with the triplet state of anthraquinone-2-sulphonate kNCP,3AQ2S*=(5.90±0.43)·108M−1s−1, and is poorly reactive toward CO3−. The kNCP,3AQ2S* value is representative of reaction with the triplet states of chromophoric dissolved organic matter. The inclusion of photochemical reactivity data into a model of surface–water photochemistry allowed the NCP transformation kinetics to be predicted as a function of water chemical composition and column depth. Very good agreement between model predictions and field data was obtained for the shallow lagoons of the Rhône delta (Southern France).
Structure | Name/CAS No. | Molecular Formula | Articles |
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2-nitro-4-chlorophenol
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C6H4ClNO3 |
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