首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >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
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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

机译:聚二甲基硅氧烷/金属有机骨架涂层涂覆的搅拌棒吸附萃取与高效液相色谱-紫外检测器联用,用于测定环境水样品中的雌激素

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摘要

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/MOFs coatings were characterized and critically compared for the extraction of seven target estrogens (17-β-estradiol, dienestrol, diethylstilbestrol, estrone, 4-t-octylphenol, bisphenol-A and 17α-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. μg/L. The linear range was 2-2500. μg/L for 17α-ethynylestradiol and 1-2500. μg/L for other estrogens. The relative standard deviations (RSDs) were in the range of 3.7-9.9% (n=8, c=20. μg/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.
机译:在这项工作中,在搅拌棒吸附萃取(SBSE)和新型聚二甲基硅氧烷(PDMS)/ MOF(包括PDMS / MOF)中引入了三种金属有机骨架(MOF)MOF-5,MOF-199和IRMOF-3 -5,PDMS / MOF-199和PDMS / IRMOF-3)涂覆的搅拌棒通过溶胶-凝胶技术制备。对这些PDMS / MOFs涂层进行了表征并严格比较了SBSE萃取的7种目标雌激素(17-β-雌二醇,二烯雌酚,二乙基雌甾醇,雌酮,4-叔辛基苯酚,双酚A和17α-乙炔基雌二醇)的结果。结果表明,PDMS / IRMOF-3表现出最高的提取效率。基于上述事实,开发了PDMS / IRMOF-3涂层SBSE-高效液相色谱紫外(HPLC-UV)检测的新方法,用于测定环境水中的七种目标雌激素。研究了影响SBSE萃取七种目标雌激素的几个参数(PDMS / IRMOF-3),包括萃取时间,搅拌速率,pH,离子强度,解吸溶剂和解吸时间。在最佳实验条件下,发现的检出限(LOD,S / N. = 3)在0.15-0.35范围内。微克/升线性范围是2-2500。 17g-乙炔雌二醇和1-2500的μg/ L。其他雌激素微克/升。相对标准偏差(RSD)在3.7-9.9%的范围内(n = 8,c = 20。g / L),富集系数为30.3至55.6倍(理论富集系数为100倍)。该方法成功地用于环境水样中雌激素的分析,并获得了加标实验的定量回收率。

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