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Quantification of Synthetic Organic Chemicals in Biological Treatment Process Effluent Using Solid-Phase Microextraction and Gas Chromatography

Benjamin S. Magbanua Jr., Dennis R. Mitchell, Steven M. Fehniger, Rebecca L. Bowyer and C. P. Leslie Grady Jr.
Water Environment Research
Vol. 72, No. 1 (Jan. - Feb., 2000), pp. 98-104
Stable URL: http://www.jstor.org/stable/25045342
Page Count: 7
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Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Quantification of Synthetic Organic Chemicals in Biological Treatment Process Effluent Using Solid-Phase Microextraction and Gas Chromatography
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Abstract

Solid-phase microextraction (SPME), a technique that uses a polymer-coated, fused-silica fiber to selectively extract organic analytes from a sample matrix, followed by gas chromatography (GC), was used to quantify selected synthetic organic chemicals (SOCs) in biological reactor effluent. By selecting an appropriate combination of SPME fiber, GC column, and GC detector, assays to quantify either a suite of SOCs or single selected SOCs were developed. Phenol, 4-chlorophenol, 2-nitrophenol, 4-nitrophenol, 2,4-dinitrophenol, isophorone, m-toluate, m-xylene, and di-n-butylphthalate were quantified simultaneously using an 85-μm polyacrylate SPME fiber, a 5% diphenyl-95% dimethyl polysiloxane capillary column, and a flame ionization detector. m-Xylene was quantified using a 100-μm polydimethylsiloxane SPME fiber, a 5% diphenyl-95% dimethyl polysiloxane capillary column, and a mass spectrometric detector. Dichloromethane was quantified using an 85-μm polyacrylate SPME fiber, a Carbopack B/1% SP-1000 packed column, and an electron capture detector. All three assays enabled detection of the target analytes to low concentrations (μg/L) with minimal sample volume and processing requirements.

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