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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 351 (1995), S. 752-757 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Two different extraction procedures to determine alachlor (2-chloro-2′,6′-diethyl-N-methoxymethyl-acetanilide) and its metabolites 2,6-diethylaniline (DEA) and 2-chloro-2′,6′-diethylacetanilide (CDEA) at very low concentration levels in groundwater are compared. Both methods were performed during a field leaching study and laboratory soil column experiments. Solid phase extraction (SPE) is characterized by the enrichment of 11 water samples at 1 g RP-C18 material, while micro liquid/liquid extraction (MLLE) means that 400 ml water samples saturated with sodium chloride were extracted once with 500 μl of toluene. Both methods differ in their concentration factors, i.e. 5000 for SPE and 800 for MLLE. The determination limits for alachlor determined as the lowest spiked concentration analyzed are 10 ng/l with SPE and 25 ng/l with MLLE. Even though the determination limits of the two methods are similar, the volatile metabolite 2,6-diethylaniline was not sufficiently recovered by SPE. Furthermore, SPE is more expensive and time consuming than MLLE. The latter is simple in use, rapidly performed and needs no evaporation step and clean-up before GC analysis. This is of special advantage for the analysis of 2,6-diethylaniline. The determination limits of the metabolites CDEA and DEA analyzed by MLLE are 25 ng/l. The extracts from both methods were directly analyzed by gas chromatography using electron capture and nitrogen-phosphorus detection.
    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. 83-88 
    ISSN: 0935-6304
    Keywords: Large volume injection ; programmed-temperature vaporizer ; organic acids ; phenols ; derivatization ; trimethylsulfonium hydroxide ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: ---The combination of on-line methylation using trimethylsulfonium hydroxide with large volume injection of 100 μL was evaluated for the analysis of organic acids and phenols in water. Solvent split injection was applied with complete evaporation of the solvent before analytes were transferred onto the GC column. Despite complete solvent removal, losses were very low compared to conventional splitless injection even for volatile acidic compounds such as propionic acid and phenol. This is explained by intermediate formation of low volatility trimethylsulfonium salts of the analytes which were held in the injector for long evaporation times of up to 10 min, if the evaporation temperature was as low as 10°C. Using a simple liquid/liquid extraction procedure, volatile fatty acids, dicarboxylic acids, benzoic acids and phenols could be detected in 5 mL of water at concentrations of 0.04-0.1 μmol/L with GC/MS in full scan mode. Lactic, pyruvic, and also malonic acids could only be detected at higher levels because of their limited extractability from water as well as their poorer methylation yields. The method provides an easy way to sensitively detect acidic compounds of medium to high volatility in water. It was applied for screening of organic acids and phenols in batch cultures of anaerobic bacteria of which one example is shown.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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