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Coupled HPLC with HRGC                                           37


































                           Figure 2.16 Chromatograms of a pentane extract of a water sample containing 200 ppb of a
                           naphtha fraction: (a) sample extracted by using a continuous flow system, where a pressurized
                           bottle was employed as the sample-delivery system; (b) batch-extracted sample. Reprinted
                           from Journal of Chromatography, A 330, J. Roeraade, ‘Automated monitoring of organic trace
                           components in water. I. Continuous flow extraction together with on-line capillary gas chro-
                           matography’, pp. 263–274, copyrigth 1985, with permission from Elsevier Science.




                           such a system with an atomic emission detector (AED) for the analysis of nitrogen-
                           chlorine- and sulfur-containing pesticides in aqueous samples (39), as shown in
                           Figure 2.19.



                           2.5.3  OPEN TUBULAR TRAPPING

                           The analysis of organic compounds from aqueous samples is also possible by using
                           open tubular trapping (OTT) columns (13, 40–42).  The extraction step involves
                           sorption of the analytes from water (40) into the stationary phase of an open tube
                           (5 m   0.53 mm id) with a film of CP-Sil-5CB (5 m film thick). Removal of water
                           is achieved by purging the trap with nitrogen, and desorption of the analytes with an
                           organic solvent (75  l). Solvent elimination prior to transfer to the GC column is
                           carried out by using a PTV injector and a multidimensional system (Figure 2.20).
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