首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Comparative study of analytical methods involving gas chromatography-mass spectrometry after derivatization and gas chromatography-tandem mass spectrometry for the determination of selected endocrine disrupting compounds in wastewaters
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Comparative study of analytical methods involving gas chromatography-mass spectrometry after derivatization and gas chromatography-tandem mass spectrometry for the determination of selected endocrine disrupting compounds in wastewaters

机译:衍生化后气相色谱-质谱和气相色谱-串联质谱法测定废水中内分泌干扰素的分析方法的比较研究

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Two GC-MS methods, based on the application of N,O-bis(trimethylsilyl)trifluoroacetamide-derivatization-GC-MS (selected-ion monitoring) and GC-MS-MS without derivatization, respectively, were optimised and applied to the determination of a group of five selected endocrine disrupting compounds (EDCs) in wastewaters. Both methods included solid-phase extraction with Oasis HLB cartridges allowing an enrichment factor for wastewater samples of 100-fold. The investigated EDCs were estrone, 17beta-estradiol, 17alpha-ethynylestradiol, 4-tert-octylphenol and bisphenol A. Results obtained from the validation studies yielded comparable results in both cases. Recoveries in spiked wastewaters at 50 ng/l were higher than 90% for all the compounds, except for 4-tert-octylphenol(75 %). Repeatability and reproducibility were adequate, varying from 1.6 to 14%, except for estrone which reproducibility was 28% when the derivatization-GC-MS method was applied. Limits of detection calculated ranged from 2.5 to 27.5 ng/l with differences between both methods from 1.1 (estrone) to 10.4 (bisphenol A) times. Both methods were successfully applied to the analysis of the target compounds in sewage treatment plant influents and effluents. Traces of bisphenol A, 4-tert-octylphenol, estrone and 17beta-estradiol were detected at concentration levels ranging from 13.3 to 1105.2 ng/l. (C) 2004 Elsevier B.V. All rights reserved.
机译:基于N,O-双(三甲基甲硅烷基)三氟乙酰胺衍生化GC-MS(选择离子监测)和未衍生化GC-MS-MS的两种GC-MS方法分别进行了优化,并用于测定废水中一组五种选定的内分泌干扰化合物(EDC)。两种方法都包括使用Oasis HLB柱进行固相萃取,使废水样品的富集系数提高了100倍。研究的EDC为雌酮,17β-雌二醇,17α-乙炔基雌二醇,4-叔辛基苯酚和双酚A。从验证研究中获得的结果在两种情况下均具有可比的结果。除4-叔辛基苯酚(75%)外,所有化合物的加标废水中50 ng / l的回收率均高于90%。重复性和重现性足够,从1.6%到14%不等,但雌酮除外,使用衍生化GC-MS方法时雌酮的重现性为28%。计算的检测限范围为2.5至27.5 ng / l,两种方法之间的差异为1.1(雌酮)至10.4(双酚A)倍。两种方法均成功地用于分析污水处理厂进水和出水中的目标化合物。在浓度范围为13.3至1105.2 ng / l的范围内检测到痕量的双酚A,4-叔辛基苯酚,雌酮和17β-雌二醇。 (C)2004 Elsevier B.V.保留所有权利。

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