4.2 Article

A screening method for polycyclic aromatic hydrocarbons determination in water by headspace SPME with GC-FID

期刊

CHROMATOGRAPHIA
卷 66, 期 9-10, 页码 773-777

出版社

SPRINGER HEIDELBERG
DOI: 10.1365/s10337-007-0371-y

关键词

gas chromatography; headspace solid-phase microextraction; experimental design; polycyclic aromatic hydrocarbons; water analysis

向作者/读者索取更多资源

A simple method for determination of polycyclic aromatic hydrocarbons (PAHs) in water using headspace solid-phase microextraction (HS-SPME) with gas chromatography-flame ionisation detector (GC-FID) was developed. In order to obtain the convenient experimental conditions for HS-SPME extraction an experimental design with two steps was accomplished. A 2(6-2) fractional factorial design and central composite design (CCD) considering three significant factors were used. Naphthalene, anthracene and fluoranthene were chosen as representatives of two, three and four aromatic rings, and the global response of three PAHs was used for the results, evaluation. The chosen extraction conditions were: 85 mu m polyacrylate fibre; 50 degrees C temperature; 60 min time; 20 mL-dissolution volume (in 40 mL glass vial); without salt addition; and 2 min desorption time. The procedure was extended to other seven PAHs (acenaphthylene, acenaphthene, fluorene, phenanthrene, pyrene, chrysene and benzo(a)anthracene) and the analytical characteristics were checked. The limit of detection (LOD) was from 0.08 (anthracene) to 0.20 mu g L-1 (naphthalene). The precision expressed as relative standard deviation (RSD in %) using 50 mu g L-1 of each analyte ranged from 6.8 to 17%. The method was applied to the analysis of the surface waters and leaching waters of contaminated soils from Gipuzkoa (North Spain). The PAHs were not detected in surface water samples. Most of the PAHs were found in the leachates from contaminated soils showing a maximum global value of 75.5 mu g L-1.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据