Title: | Calibration of a commercial solid-phase microextraction device for measuring headspace concentrations of organic volatiles |
Address: | "USDA Agricultural Research Service, National Center for Agricultural Utilization Research, Bioactive Agents Research Unit, 1815 North University Street, Peoria, Illinois 61604" |
ISSN/ISBN: | 0003-2700 (Print) 0003-2700 (Linking) |
Abstract: | "Solid-phase microextraction (SPME) is a versatile new technique for collecting headspace volatiles prior to GC analysis. The commercial availability of uniform SPME fibers makes routine, practical quantitation of headspace concentrations possible, but straightforward information for relating GC peak areas from SPME analyses to headspace concentrations has not been available. The calibration factors (amount absorbed by the fiber divided by headspace concentration) were determined for 71 compounds using SPME fibers with a 100 mum poly(dimethylsiloxane) coating. The compounds ranged from 1 to 16 carbons in size and included a variety of functional groups. Calibration factors varied widely, being 7000 times higher for tetradecane than for acetaldehyde. Most compounds with a Kovats retention index of <1300 on a nonpolar GC column (DB-1) equilibrated with the fiber in 30 min or less. A regression model is presented for predicting the calibration factor from GC retention index, temperature, and analyte functional class. The calibration factor increased with retention index but decreased with increasing sampling temperature. For a given retention index, polar compounds such as amines and alcohols were absorbed by the fibers in greater amounts than were hydrocarbons. Henry's law constants determined using SPME were in general agreement with literature values, which supported the accuracy of the measured calibration factors. An unexpected concentration dependence of calibration factors was noted, especially for nitrogen-containing and hydroxy compounds; calibration factors were relatively higher (the SPME fiber was more sensitive) at the lower analyte concentrations" |
Notes: | "PubMed-not-MEDLINEBartelt, R J eng 1997/02/01 Anal Chem. 1997 Feb 1; 69(3):364-72. doi: 10.1021/ac960820n" |