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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 7 (1995), S. 383-394 
    ISSN: 1040-7685
    Keywords: large-volume injection ; gas chromatography ; on-column injector ; environmental analysis ; organophosphorus pesticides ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Large-volume injection is an attractive means to improve detection limits when analyzing dilute sample extracts. There is now no need to achieve enrichment by means of solvent evaporation, which makes the total analytical procedure less reliable and less robust due to loss of volatile compounds. In this study on-column injection was applied for large-volume injection using an on-column injector in combination with a deactivated uncoated fused silica capillary (retention gap) and an early solvent vapor exit. Two strategies are described. The first one relies on the programmable speed of an infusion pump, which is adapted such that it lies just above the evaporation rate of the extraction solvent used. With the second procedure, which can be used for a commercially available autosampler, the evaporation speed is adjusted to the fixed speed of injection by varying the temperature during injection. During optimization the additional solvent evaporation time was determined. The optimum conditions for an injection volume of 100 μL of either n-hexane or ethyl acetate are reported. Large-volume injection was used for simplified and miniaturized solid-phase extraction procedures. The procedures were used to determine various organic micropollutants, such as organophosphorus pesticides and triazine herbicides, in tap and surface water extracts, using a flame photometric, and a mass spectrometric detector. For both methods good recovery for most of the analytes (70-87%), linear calibration curves (0.01-5 μg/L range), and relative standard deviations of less than 10% were obtained. Detection limits typically were in the range of 1-10 ng/L for GC-FPD and 10-150 ng/L for GC-MS. When working in the time-scheduled multiple ion detection mode detection limits in GC-MS were one order of magnitude lower. © 1995 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 19 (1998), S. 2753-2776 
    ISSN: 0173-0835
    Keywords: Capillary electrophoresis ; Capillary electrochromatography ; Analyte identification ; Spectrometric detection ; Review ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A review on applications of on-line hyphenation in capillary electrophoresis and capillary electrochromatography for the identification of migrating analytes is presented. There is an urgent need for unambiguous analyte identification by combining spectral information and observed migration times, because the parameters influencing the migration times and separation efficiencies in these separation techniques are not easily controlled, especially when real samples containing unknown interferences have to be analyzed. The spectrometric techniques covered here are ultraviolet and visible radiation (UV/Vis) absorption, fluorescence including fluorescence line-narrowing spectroscopy, Raman spectroscopy, nuclear magnetic resonance and mass spectrometry. Attention is essentially confined to literature reports in which the extra information provided by the detector is really used for identification purposes, especially in real-life samples, while the interfacing as such and analyte detectabilities in standard solutions are only briefly discussed. This article covers an extensive fraction of the literature published on this topic until the beginning of 1998.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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