4.6 Article

Polydimethylsiloxane/metal-organic frameworks coated stir bar sorptive extraction coupled to high performance liquid chromatography-ultraviolet detector for the determination of estrogens in environmental water samples

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1310, Issue -, Pages 21-30

Publisher

ELSEVIER
DOI: 10.1016/j.chroma.2013.08.047

Keywords

SBSE; PDMS/MOFs coating; Estrogens; HPLC-UV; Environmental water samples

Funding

  1. National Nature Science Foundation of China [20775057]
  2. Science Fund for Creative Research Groups of NSFC [20621502, 20921062]
  3. State Key Laboratory of Environmental Chemistry and Ecotoxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences [KF2010-04]

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In this work, three kinds of metal-organic frameworks (MOFs), MOF-5, MOF-199 and IRMOF-3, were introduced in stir bar sorptive extraction (SBSE) and novel polydimethylsiloxane (PDMS)/MOFs (including PDMS/MOF-5, PDMS/MOF-199 and PDMS/IRMOF-3) coated stir bars were prepared by sol-gel technique. These PDMS/MOF5 coatings were characterized and critically compared for the extraction of seven target estrogens (17-beta-estradiol, dienestrol, diethylstilbestrol, estrone, 4-t-octylphenol, bisphenol-A and 17 alpha-ethynylestradiol) by SBSE, and the results showed that PDMS/IRMOF-3 exhibited highest extraction efficiency. Based on the above facts, a novel method of PDMS/IRMOF-3 coating SBSE-high performance liquid chromatography ultraviolet (HPLC-UV) detection was developed for the determination of seven target estrogens in environmental waters. Several parameters affecting extraction of seven target estrogens by SBSE (PDMS/IRMOF-3) including extraction time, stirring rate, pH, ionic strength, desorption solvent and desorption time were investigated. Under the optimal experimental conditions, the limits of detection (LODs, S/N = 3) were found to be in the range of 0.15-0.35 mu g/L. The linear range was 2-2500 mu g/L for 17 alpha-ethynylestradiol and 1-2500 mu g/L for other estrogens. The relative standard deviations (RSDs) were in the range of 3.7-9.9% (n = 8, c = 20 mu g/L) and the enrichment factors were from 30.3 to 55.6-fold (theoretical enrichment factor was 100-fold). The proposed method was successfully applied to the analysis of estrogens in environmental water samples, and quantitative recoveries were obtained for the spiking experiments. (C) 2013 Elsevier B.V. All rights reserved.

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