期刊
WATER RESEARCH
卷 46, 期 19, 页码 6309-6318出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.watres.2012.09.012
关键词
Fe-III-TAML; Fe-III-B*; EE2; Estrogenicity; Catalysis; Oxidation; Daughter products
资金
- University of Auckland
The oxidative degradation of the oral contraceptive 17 alpha-ethinylestradiol (EE2) in water by a new advanced catalytic oxidation process was investigated. The oxidant employed was hydrogen peroxide in aqueous solution and the catalyst was the iron tetra-amido macrocyclic ligand (Fe-III-TAML) complex that has been designated Na[Fe(H2O)(B*)] (Fe-III-B*). EE2 (10 mu M) was oxidised rapidly by the Fe-III-B*/H2O2 (5 nW4 mM) catalytic oxidation system at 25 degrees C, and for reactions at pH 8.40-11.00, no unchanged EE2 was detected in the reaction mixtures after 60 min. No oxidation of EE2 was detected in blank reactions using either H2O2 or Fe-III-B* alone. The maximum rate of EE2 loss occurred at pH 10.21. At this pH the half-life of EE2 was 2.1 min and the oxidised products showed around 30% estrogenicity removal, as determined by the yeast estrogen screen (YES) bioassay. At pH 11.00, partial oxidation of EE2 by Fe-III-B*/H2O2 (5 nW4 mM) was studied (half-life of EE2 was 14.5 min) and in this case the initial intermediates formed were a mixture of the epimers 17 alpha-ethynyl-1,4-estradiene-10 alpha,17 beta-diol-3-one (1a) and 17 alpha-ethynyl-1,4-estradiene-10 beta,17 beta-diol-3-one (1b) (identified by LC-ToF-MS and H-1 NMR spectroscopy). Significantly, this product mixture displayed a slightly higher estrogenicity than EE2 itself, as determined by the YES bioassay. Upon the addition of further aliquots of Fe-III-B* (to give a Fe-III-B* concentration of 500 nM) and H2O2 (to bring the concentration up to 4 mM assuming the final concentration had dropped to zero) to this reaction mixture the amounts of la and 1b slowly decreased to zero over a 60 min period as they were oxidised to unidentified products that showed no estrogenicity. Thus, partial oxidation of EE2 gave products that have slightly increased estrogenicity, whereas more extensive oxidation by the advanced catalytic oxidation system completely removed all estrogenicity. These results underscore the importance of controlling the level of oxidation during the removal of EE2 from water by oxidative processes. (C) 2012 Elsevier Ltd. All rights reserved.
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