Analysis of estrogens in environmental waters using polymer monolith in-polyether ether ketone tube solid-phase microextraction combined with high-performance liquid chromatography

التفاصيل البيبلوغرافية
العنوان: Analysis of estrogens in environmental waters using polymer monolith in-polyether ether ketone tube solid-phase microextraction combined with high-performance liquid chromatography
المؤلفون: Yu-Qi Feng, Bingsheng Zhou, Yi Wen, Shi-Wei Jin, Ying Xu
المصدر: Journal of Chromatography A. 1133:21-28
بيانات النشر: Elsevier BV, 2006.
سنة النشر: 2006
مصطلحات موضوعية: Monolithic HPLC column, Polymers, Chemical Fractionation, Endocrine Disruptors, Solid-phase microextraction, Biochemistry, High-performance liquid chromatography, Polyethylene Glycols, Analytical Chemistry, Benzophenones, Polyether ether ketone, chemistry.chemical_compound, Sample preparation, Phosphoric acid, Chromatography, High Pressure Liquid, Detection limit, Chromatography, Organic Chemistry, Extraction (chemistry), Reproducibility of Results, Water, General Medicine, Ketones, chemistry, Microscopy, Electron, Scanning, Water Pollutants, Chemical
الوصف: A simple, rapid and sensitive on-line method for simultaneous determination of four endocrine disruptors (17 beta-estradiol, estriol, bisphenol A and 17 alpha-ethinylestradiol) in environmental waters was developed by coupling in-tube solid-phase microextraction (SPME) to high-performance liquid chromatography (HPLC) with fluorescence detection (FLD). A poly(acrylamide-vinylpyridine-NAP-methylene bisacrylamide) monolith, synthesized inside a polyether ether ketone (PEEK) tube, was selected as the extraction medium. To achieve optimum extraction performance, several parameters were investigated, including extraction flow-rate, extraction time, and pH value, inorganic salt and organic solvent content of the sample matrix. By simply filtered with nylon membrane filter and adjusting the pH of samples to 6.0 with phosphoric acid, the sample solution then could be directly injected into the device for extraction. Low detection limits (S/N = 3) and quantification limits (S/N = 10) of the proposed method were achieved in the range of 0.006-0.10 ng/mL and 0.02-0.35 ng/mL from spiked lake waters, respectively. The calibration curves of four endocrine disruptors showed good linearity ranging from quantification limits to 50 ng/mL with a linear coefficient R-2 value above 0.9913. Good method reproducibility was also found by intra- and inter-day precisions, yielding the RSDs less than 12 and 9.8%, respectively. Finally, the proposed method was successfully applied to the determination of these compounds in several environmental waters. (c) 2006 Elsevier B.V. All rights reserved.
تدمد: 0021-9673
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3837412c63b3a171e1b1fa9268b4406b
https://doi.org/10.1016/j.chroma.2006.08.049
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....3837412c63b3a171e1b1fa9268b4406b
قاعدة البيانات: OpenAIRE