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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 21 (1998), S. 450-456 
    ISSN: 0935-6304
    Keywords: Drying cartridge ; gas chromatography ; solid-phase extraction ; microcontaminants ; water samples ; on-line SPE-GC ; mass spectrometric detection ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---A drying cartridge was used and optimized for the in-line elimination of water from the desorption eluent in on-line solid phase extraction-gas chromatography (SPE-GC). The cartridge is essentially a small stainless-steel precolumn packed with a drying agent which can be regenerated by simultaneous heating and purging with a moisture-free gas. The drying cartridge was mounted on an additional valve instead of between the SPE-GC transfer valve and the on-column injector to enable regeneration of the cartridge during the GC run and, thus, to increase sample throughput. Three drying agents were tested, viz. sodium sulfate, silica, and molecular sieves. Although molecular sieves have the highest capacity, silica was preferred because of practical considerations. Large-volume injections were performed through the in-line drying cartridge using a mixture of 23 microcontaminants ranging widely in polarity and volatility. Four solvents were tested. With pentane and hexane, the more polar analytes were retained by the drying cartridge. Ethyl acetate and methyl acetate gave much better (and closely similar) recoveries for all analytes. Because water elimination on the silica cartridge proved to be less critical than with ethyl acetate, this solvent was finally selected. The entire SPE-drying cartridge-GC set-up was combined with mass spectrometric (MS) detection for the determination of a mixture of micropollutants in real-life water samples. With 10-ml tap water samples spiked at the 0.5 μg/l level, for the majority of the test compounds the analyte recoveries generally were 60-106%, and (full-scan) detection limits typically were 0.01-0.03 μg/l. Some very polar analytes such as, e.g. dimethoate, were (partially) sorbed onto the silica packing of the drying cartridge.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 22 (1999), S. 459-464 
    ISSN: 0935-6304
    Keywords: Fast gas chromatography ; gas chromatography ; resistive heating ; organophosphorus pesticides ; PAHs ; triazines ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---The features of a resistive-heated capillary column for fast temperature-programmed gas chromatography (GC) have been evaluated. Experiments were carried out using a commercial available EZ Flash GC, an assembly which can be used to upgrade existing gas chromatographs. The capillary column is placed inside a metal tube which can be heated, and cooled, much more rapidly than any conventional GC oven. The EZ Flash assembly can generate temperature ramps up to 1200°/min and can be cooled down from 300 to 50°C in 30 s. Samples were injected via a conventional split/splitless injector and transferred to the GC column. The combination of a short column (5 m×0.25 mm i. d.), a high gas flow rate (up to 10 mL/min), and fast temperature programmes typically decreased analysis times from 30 min to about 2.5 min. Both the split and splitless injection mode could be used. With n-alkanes as test analytes, the standard deviations of the retention times with respect to the peak width were less than 15% (n = 7). First results on RSDs of peak areas of less than 3% for all but one n-alkane indicate that the technique can also be used for quantification. The combined use of a short GC column and fast temperature gradients does cause some loss of separation efficiency, but the approach is ideally suited for fast screening as illustrated for polycyclic aromatic hydrocarbons, organophosphorus pesticides, and triazine herbicides as test compounds. Total analysis times - which included injection, separation, and equilibration to initial conditions - were typically less than 3 min.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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