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Simultaneous determination of 22 volatile organic compounds, methyl-tert-butyl ether, 1,4-dioxane, 2-methylisoborneol and geosmin in water by headspace ... [An article from: Analytica Chimica Acta]


by S. Nakamura, S. Daishima

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Studio: Elsevier
Binding: Digital
Publication Date: August 30, 2008
Publisher: Elsevier


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This digital document is a journal article from Analytica Chimica Acta, published by Elsevier in . The article is delivered in HTML format and is available in your Amazon.com Media Library immediately after purchase. You can view it with any web browser.

Description:
A method for the simultaneous determination of 22 volatile organic compounds (VOCs), methyl-tert-butyl ether (MTBE), 1,4-dioxane, 2-methylisoborneol (2-MIB) and geosmin in water by headspace solid phase microextraction (SPME)-gas chromatography-mass spectrometry (GC-MS) is described. Three types of SPME fibers (carboxen (CAR)/polydimethylsiloxane (PDMS), divinylbenzene (DVB)/PDMS and 100-@mm PDMS) were evaluated to achieve the method detection limits and linear range required in Japanese water regulation. A 100-@mm PDMS was found to be the best coating to obtain a wide range of linearity for the target compounds in multiple-component system. CAR/PDMS and DVB/PDMS of adsorbent type fibers showed a narrow linear range for 22 VOCs, MTBE and 1,4-dioxane at the @mg/l levels due to the limited capacity. The detection limits of this method were 0.01-0.05@mg/l for 22 VOCs, 0.01@mg/l for MTBE, 1.2@mg/l for 1,4-dioxane, 0.6ng/l for 2-MIB and 0.3ng/l for geosmin. The recoveries of 22 VOCs and MTBE from a river water sample spiked at 1@mg/l were between 93.7 and 104.0%, with R.S.D. values of between 1.7 and 9.5%. Those of 1,4-dioxane, 2-MIB and geosmin at 5@mg/l, 10ng/l and 10ng/l, respectively, were 109.1, 95.9 and 97.4%, with R.S.D. values of 2.0, 5.6 and 1.8%. The method provided linear range from 0.1 to 100@mg/l for 21 VOCs and MTBE, 0.1 to 50@mg/l for m,p-xylene, 5 to 100@mg/l for 1-4dioxane and 1 to 100ng/l for 2-MIB and geosmin.
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