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DOI10.1016/j.chroma.2017.03.006
An ultra-sensitive method for the analysis of perfluorinated alkyl acids in drinking water using a column switching high-performance liquid chromatography tandem mass spectrometry
Dasu, Kavitha1,2; Nakayama, Shoji F.3; Yoshikane, Mitsuha4; Mills, Marc A.; Wright, J. Michael2,5; Ehrlich, Shelley6
发表日期2017-04-21
ISSN0021-9673
卷号1494页码:46-54
英文摘要

In epidemiological research, it has become increasingly important to assess subjects' exposure to different classes of chemicals in multiple environmental media. It is a common practice to aliquot limited volumes of samples into smaller quantities for specific trace level chemical analyses. A novel method was developed for the determination of 14 perfluorinated alkyl acids (PFAAs) in small volumes (10 mL) of drinking water using off-line solid phase extraction (SPE) pre-treatment followed by on-line pre-concentration on a WAX column before analysis on column-switching high performance liquid chromatography tandem mass spectrometry (HPLC-MS/MS). In general, large volumes (100-1000 mL) have been used for the analysis of PFAAs in drinking water. The current method requires approximately 10 mL of drinking water concentrated by using an SPE cartridge and eluted with methanol. A large volume injection of the extract was introduced on to a column-switching HPLC-MS/MS using a mix-mode SPE column for the trace level analysis of PFAAs in water. The recoveries for most of the analytes in the fortified laboratory blanks ranged from 73 +/- 14% to 128 +/- 5%. The lowest concentration minimum reporting levels (LCMRL) for the 14 PFAAs ranged from 0.59 to 3.4 ng/L. The optimized method was applied to a pilot-scale analysis of a subset of drinking water samples from an epidemiological study. These samples were collected directly from the taps in the households of Ohio and Northern Kentucky, United States and the sources of drinking water samples are both surface water and ground water, and supplied by different water distribution facilities. Only five PFAAs, perfluoro-1-butanesulfonic acid (PFBS), perfluoro-1- -hexanesulfonic acid (PFHxS), perfluoro-1-octanesulfonic acid (PFOS), perfiuoro-n-heptanoic acid (PFHpA) and perfluoron-octanoic acid (PFOA) are detected above the LCMRL values. The median concentrations of these five PFAAs detected in the samples was <4.1 ng/L with PFOS at 7.6 ng/L and PFOA at 10 ng/L. Concentrations of perfluoro-1-decanesulfonic acid, PFDS and other perfluoroalkyl carboxylic acids were below the LCMRL values. (C) 2017 Elsevier B.V. All rights reserved.


英文关键词Perfluorinated alkyl acids;Column-switching HPLC;Drinking water;Solid phase extraction
语种英语
WOS记录号WOS:000399512100005
来源期刊JOURNAL OF CHROMATOGRAPHY A
来源机构美国环保署
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/61039
作者单位1.Natl Acad Sci, Natl Res Council, Engn, Med, 500 Fifth St NW, Washington, DC 20001 USA;
2.US EPA, Natl Risk Management Res Lab, Cincinnati, OH USA;
3.Natl Inst Environm Studies, Ctr Hlth & Environm Risk Res, Tsukuba, Ibaraki, Japan;
4.IDEA Consultants Inc, Inst Environm Ecol, Environm Risk Res Ctr, Tokyo, Japan;
5.US EPA, Natl Ctr Environm Assessment, Cincinnati, OH 45268 USA;
6.Univ Cincinnati, Coll Med, Cincinnati Childrens Hosp Med Ctr, Div Biostat & Epidemiol, Cincinnati, OH USA
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GB/T 7714
Dasu, Kavitha,Nakayama, Shoji F.,Yoshikane, Mitsuha,et al. An ultra-sensitive method for the analysis of perfluorinated alkyl acids in drinking water using a column switching high-performance liquid chromatography tandem mass spectrometry[J]. 美国环保署,2017,1494:46-54.
APA Dasu, Kavitha,Nakayama, Shoji F.,Yoshikane, Mitsuha,Mills, Marc A.,Wright, J. Michael,&Ehrlich, Shelley.(2017).An ultra-sensitive method for the analysis of perfluorinated alkyl acids in drinking water using a column switching high-performance liquid chromatography tandem mass spectrometry.JOURNAL OF CHROMATOGRAPHY A,1494,46-54.
MLA Dasu, Kavitha,et al."An ultra-sensitive method for the analysis of perfluorinated alkyl acids in drinking water using a column switching high-performance liquid chromatography tandem mass spectrometry".JOURNAL OF CHROMATOGRAPHY A 1494(2017):46-54.
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