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« Previous AbstractDetermination of volatile organic hydrocarbons in water samples by solid-phase dynamic extraction    Next AbstractMethod Development for Detecting Low Level Volatile Organic Compounds (VOCs) among Workers and Residents from a Carpentry Work Shop in a Palestinian Village »

J Chromatogr A


Title:In-tube extraction for enrichment of volatile organic hydrocarbons from aqueous samples
Author(s):Jochmann MA; Yuan X; Schilling B; Schmidt TC;
Address:"Instrumental Analytical Chemistry, University Duisburg-Essen, Lotharstrasse 1, D-47048 Duisburg, Germany"
Journal Title:J Chromatogr A
Year:2008
Volume:20071203
Issue:2
Page Number:96 - 105
DOI: 10.1016/j.chroma.2007.11.100
ISSN/ISBN:0021-9673 (Print) 0021-9673 (Linking)
Abstract:"In-tube extraction (ITEX) is a novel solventless extraction technique in which a headspace syringe with a needle body filled with a sorbent (here: Tenax TA) is used. The analytes are extracted from sample headspace by dynamic extraction. The needle body is surrounded by a separate heater, which is used for thermal desorption of analytes into the injection port of a GC system. We report here for the first time the optimization and evaluation of a fully automated analytical method based on ITEX. As target analytes, 19 common groundwater contaminants such as halogenated volatiles and monoaromatic compounds have been chosen. Method related parameters such as extraction temperature, number of extraction cycles, extraction and desorption volume as well as extraction and desorption flow rates were investigated in detail. The linear dynamic range of the ITEX method ranged over six orders of magnitude between 0.028 microg/L and 1218 microg/L with linear correlation coefficients between 0.990 and 0.998 for the investigated compounds. Method detection limits for monoaromatic compounds were between 28 ng/L (ethylbenzene) and 68 ng/L (1,2,4-trimethylbenzene). For halogenated volatile organic compounds, method detection limits between 48 ng/L (chloroform) and 799 ng/L (dichloromethane) were obtained. The precision of the method with external calibration was between 3.1% (chloroform ethylbenzene) and 7.4% (1,2,3-trimethylbenzene)"
Keywords:"Benzene Derivatives/*analysis Chemical Fractionation/instrumentation/*methods Gas Chromatography-Mass Spectrometry Volatilization Water Pollutants, Chemical/*analysis;"
Notes:"MedlineJochmann, Maik A Yuan, Xue Schilling, Beat Schmidt, Torsten C eng Evaluation Study Research Support, Non-U.S. Gov't Validation Study Netherlands 2007/12/25 J Chromatogr A. 2008 Feb 1; 1179(2):96-105. doi: 10.1016/j.chroma.2007.11.100. Epub 2007 Dec 3"

 
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