Determination of volatile organic hydrocarbons in water samples by solid-phase dynamic extraction

被引:46
作者
Jochmann, Maik A. [1 ]
Yuan, Xue [1 ]
Schmidt, Torsten C. [1 ]
机构
[1] Univ Tubingen, Ctr Appl Geosci ZAG, D-72076 Tubingen, Germany
关键词
solid-phase dynamic extraction; volatile organic compound; groundwater analysis; gas chromatography-mass spectrometry; Setschenow constants;
D O I
10.1007/s00216-006-1066-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In the present study a headspace solid-phase dynamic extraction method coupled to gas chromatography-mass spectrometry (HS-SPDE-GC/MS) for the trace determination of volatile halogenated hydrocarbons and benzene from groundwater samples was developed and evaluated. As target compounds, benzene as well as 11 chlorinated and brominated hydrocarbons (vinyl chloride, dichloromethane, cis-1,2-dichloroethylene, trans-1,2-dichloroethylene, carbon tetrachloride, chloroform, trichloroethylene, tetrachloroethylene, bromoform) of environmental and toxicological concern were included in this study. The analytes were extracted using a SPDE needle device, coated with a poly(dimethylsiloxane) with 10% embedded activated carbon phase (50-mu m film thickness and 56-mm film length) and were analyzed by GC/MS in full-scan mode. Parameters that affect the extraction yield such as extraction and desorption temperature, salting-out, extraction and desorption flow rate, extraction volume and desorption volume, the number of extraction cycles, and the pre-desorption time have been evaluated and optimized. The linearity of the HS-SPDE-GC/MS method was established over several orders of magnitude. Method detection limits (MDLs) for the compounds investigated ranged between 12 ng/L for cis-dichloroethylene and trans-dichloroethylene and 870 ng/L for vinyl chloride. The method was thoroughly validated, and the precision at two concentration levels (0.1 mg/L and a concentration 5 times above the MDL) was between 3.1 and 16% for the analytes investigated. SPDE provides high sensitivity, short sample preparation and extraction times and a high sample throughput because of full automation. Finally, the applicability to real environmental samples is shown exemplarily for various groundwater samples from a former waste-oil recycling facility. Groundwater from the site showed a complex contamination with chlorinated volatile organic compounds and aromatic hydrocarbons.
引用
收藏
页码:2163 / 2174
页数:12
相关论文
共 47 条
[41]   Sampling and determination of volatile organic compounds with needle trap devices [J].
Wang, AP ;
Fang, F ;
Pawliszyn, J .
JOURNAL OF CHROMATOGRAPHY A, 2005, 1072 (01) :127-135
[42]   Development of a fiber-in-tube microextraction protocol for gas chromatography-electron capture detection of hexachlorocyclohexanes in water samples [J].
Wang, JX ;
Jiang, DQ ;
Yan, XP .
ANALYTICA CHIMICA ACTA, 2005, 545 (02) :232-238
[43]  
Wypych J, 2002, CHEM ANAL-WARSAW, V47, P507
[44]  
ZHANG Z, 1996, J HIGH RES CHROMATOG, V19, P155
[45]   HEADSPACE SOLID-PHASE MICROEXTRACTION [J].
ZHANG, ZY ;
PAWLISZYN, J .
ANALYTICAL CHEMISTRY, 1993, 65 (14) :1843-1852
[46]   Improved analysis of volatile halogenated hydrocarbons in water by purge-and-trap with gas chromatography and mass spectrometric detection [J].
Zoccolillo, L ;
Amendola, L ;
Cafaro, C ;
Insogna, S .
JOURNAL OF CHROMATOGRAPHY A, 2005, 1077 (02) :181-187
[47]   Compound-specific carbon isotope analysis of volatile organic compounds in the low-microgram per liter range [J].
Zwank, L ;
Berg, M ;
Schmidt, TC ;
Haderlein, SB .
ANALYTICAL CHEMISTRY, 2003, 75 (20) :5575-5583