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  • Trace analysis  (3)
  • Wiley-Blackwell  (3)
  • Macmillian Magazines Ltd.
  • Periodicals Archive Online (PAO)
  • 1985-1989  (3)
  • 1940-1944
  • 1
    ISSN: 0935-6304
    Keywords: Capillary gas chromatography ; Detection limits ; Trace analysis ; Narrow bore columns ; Wide bore columns ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The need for faster and more efficient separations of complex mixtures of organic compounds by gas chromatography has led to the development of small inner diameter open tubular columns. Owing to their decreased plate height, extremely narrow peaks are obtained. When differently sized columns with equal plate numbers are compared, injection of a fixed amount of a solute will give the highest detector signals for the smallest bore columns. When P is defined as the ratio of the column inlet and outlet pressures, it can be seen from theory that under normalized chromatographic conditions the minimum detectable amount (Qº) for a mass flow sensitive detector increases proportionally to the square of the column diameter for P = 1. In the situation of greater interest in the practice of open tubular gas chromatography where P is large, a linear relationship is derived between Qº and the column diameter.It is a widespread misunderstanding, however, that narrow bore capillary columns should be used for this reason in trace analysis. If a fixed relative contribution of the injection band width to the overall peak variance is allowed, a decreased plate height drastically restricts the maximum sample volume to be injected. It is shown that the minimum analyte concentration in the injected sample (Cº) is inversely proportional to the column inner diameter when a mass flow sensitive detector is used. For actual concentrations less than Cº, sample preconcentration is required. The effect of peak resolution and selectivity of the stationary phase in relation to Cº and Qº will be discussed as well. The validity of the given theory is experimentally investigated. Minimum analyte concentrations and minimum detectable amounts are compared using columns with different inner diameter.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0935-6304
    Keywords: Capillary GC ; Coupled LC-GC ; Large injection volumes ; Trace analysis ; Aqueous samples ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: This paper describes the design of a new, versatile, and low-cost on-line LC-GC interface that allows the fast and reliable introduction of large sample volumes onto a capillary GC column. The sample introduction procedure consists successively of: evaporation of the entire sample (LC fraction), selective removal of the solvent and simultaneously cold-trapping of the solutes, splitless transfer of the solutes to the GC column, on-column focusing, GC separation and detection. Quantitative and qualitative aspects of various experimental parameters are evaluated and optimum conditions are reported. The applicability of the method is demonstrated on a synthetic aqueous sample of chlorinated pesticides.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 10 (1987), S. 60-66 
    ISSN: 0935-6304
    Keywords: Capillary gas chromatography ; Cold-trapping ; Drying ; Gas stripping ; Trace analysis ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The design and features of an on-line purge and cold-trap pre-concentration device for rapid analysis of volatile organic compounds in aqueous samples are discussed. Excessive water is removed from the purge gas by a condenser or a water permeable membrane in order to avoid blocking of the capillary cold-trap. Synthetic mixtures covering concentrations ranging from tenths to tens of ppb's and different chemical classes are used to study the effect of various process factors on the efficiency and selectivity of water removal as well as on the purging recovery. The importance of the concentration of the solutes, the flow rate in conjunction with the volume of the purge gas, and the temperature of the condenser, the cold-trap and the sample is emphasized. Theoretical models describing the purge process and the blocking of the cold-trap agree fairly well with the highly reproducible experimental results (σ = 2-4%). Both the condenser and the Nafion membrane successfully remove water, although some compounds, dependent on volatility and polarity, are partly or completely lost. It is shown that non-polar volatile organic compounds are efficiently enriched so that recoveries between 80-100% and a detection limit of 1 ppt can be obtained. The applicability of the system is illustrated on some examples.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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