Fe(III)-oxalate complexes induced photooxidation of diethylstilbestrol in water.

In this work, the photooxidation of diethylstilbestrol (DES), a synthetic estrogen, was investigated in a concentric reactor under a 125 W high-pressure mercury lamp (lambda > or = 365 nm). The photooxidation efficiencies were dependent on the pH values and Fe(III)/oxalate ratios of the system, with higher efficiency at pH 3.50+/-0.05 and Fe(III)/oxalate ratio 10.0/120.0 micromol l(-1). The photooxidation reactions obeyed the law of pseudo-first-order reaction at the concentration over the range of 2.0-10.0 mg l(-1) of DES. The photooxidation rates decreased with increasing the initial concentrations of DES. For 2.0 mg l(-1) DES, the observed photooxidation rate coefficient (k(obs)) was 0.00622 min(-1). By using GC-MS and LC-MS techniques, the predominant photooxidation products DES-o-catechol ([M](+), m/z 284) and DES-4-semiquinone ([M](-), m/z 267) were respectively identified and the mechanisms for the oxidative degradation were proposed. When DES reacted with OH radicals, C atoms in 3-position were added with OH radicals to produce hydrolyzed DES radical followed by two oxidation pathways: (1) dehydrolyzing to produce DES-4-semiquinone which was oxidized further to DES-4,4'-quinone; (2) undergoing peroxidation by O(2) and getting rid of HO(2) radical to produce DES-o-catechol. After that, the two H atoms on the hydroxy group of the catechol were extracted in two individual steps to form intermediates semiquinone radical and o-quinone. The catechol intermediates underwent further oxidation, benzene ring cleavage and decarboxylation, up to mineralization ultimately.