Identification of new ozonation disinfection byproducts of 17β-estradiol and estrone in water

被引:33
作者
de Oliveira Pereira, Renata [1 ,2 ]
Lopez de Alda, Miren [2 ]
Joglar, Jesus [3 ]
Daniel, Luiz Antonio
Barcelo, Damia [2 ,4 ]
机构
[1] Univ Sao Paulo, Dept Hydraul & Sanitat, Sao Carlos Engn Sch, BR-13566590 Sao Paulo, Brazil
[2] IDAEA CSIC, Inst Environm Assessment & Water Res, Barcelona 08034, Spain
[3] Inst Adv Chem Catalonia IQAC CSIC, Dept Biol Chem & Mol Modelling, Barcelona 08034, Spain
[4] Univ Girona, Catalan Inst Water Res ICRA, Girona 17003, Spain
基金
巴西圣保罗研究基金会;
关键词
Estrogen; Drinking water; Oxidation process; Disinfection byproduct; ENDOCRINE DISRUPTING COMPOUNDS; SOLID-PHASE EXTRACTION; DRINKING-WATER; ESTROGENIC ACTIVITY; MASS-SPECTROMETRY; AQUEOUS-SOLUTION; BISPHENOL-A; EMERGING CONTAMINANTS; OXIDATION-PRODUCTS; TREATMENT PLANTS;
D O I
10.1016/j.chemosphere.2011.05.058
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Estrogens are a class of micro-pollutants found in water at low concentrations (in the ng L(-1) range), but often sufficient to exert estrogenic effects due to their high estrogenic potency. Disinfection of waters containing estrogens through oxidative processes has been shown to lead to the formation of disinfection byproducts, which may also be estrogenic. The present work investigates the formation of disinfection byproducts of 17 beta-estradiol (E2) and estrone (E1) in the treatment of water with ozone. Experiments have been carried out at two different concentrations of the estrogens in ground water (100 ng L(-1) and 100 mu g L(-1)) and at varying ozone dosages (0-30 mg L(-1)). Detection of the estrogens and their disinfection byproducts in the water samples has been performed by means of ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) with a triple quadrupole (QqQ) and a quadrupole-time of flight (QqTOF) instrument. Both E2 and El have been found to form two main byproducts, with molecular mass (MM) 288 and 278 in the case of E2, and 286 and 276 in the case of El, following presumably the same reaction pathways. The E2 byproduct with MM 288 has been identified as 10epsilon-17beta-dihydroxy-1,4-estradieno-3-one (DEO), in agreement with previously published results. The molecular structures and the formation pathways of the other three newly identified byproducts have been suggested. These byproducts have been found to be formed at both high and low concentrations of the estrogens and to be persistent even after application of high ozone dosages. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1535 / 1541
页数:7
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