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  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Bioluminescence and Chemiluminescence 4 (1989), S. 484-499 
    ISSN: 0884-3996
    Keywords: Luminescence ; chromatography ; detection ; quantitative analysis ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: An overview is presented of the physicochemical basis of luminescence, and its application to the detection of chemicals (drugs, biomedically important compounds, environmentally active substances) in liquid chromatographic systems.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1040-7685
    Keywords: solid phase extraction ; thermal desorption ; on-line ; aqueous samples ; gas chromatography ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A module for combined solid-phase extraction and thermal desorption (SPETD) was incorporated into a system for automated GC analysis. Solid-phase extraction of analytes from water could be carried out after injection of an aqueous sample of 100 μL either by a loop using the carrier gas for sample introduction or manually with a syringe. After drying of the stationary phase by the carrier gas at a high flow rate, thermal desorption could be carried out at temperatures up to 300-350°C. Suitable packing materials for the liner in the SPETD module, i.e., materials which efficiently trap the organic compounds from an aqueous solution and are sufficiently thermostable, include Tenax and carbon-based phases, as well as a silylated alkylmodified silica. With the latter, however, the problem of efficient drying after sorption still must be solved. Each phase has its own application range which, from among the analytes which are trapped during sorption, is determined at the volatile end by losses occurring during drying by helium purging, and at the nonvolatile end by losses due to incomplete release during thermal desorption. From this study (using n-alkanes, chlorobenzenes, and chlorophenols as test solutes), it appears that the Tenax phases, Tenax-TA and Tenax-GR, have the widest application range; essentially quantitative recoveries were obtained for C10 through C26 n-alkanes. The carbon-based phases appear to be useful for relatively volatile compounds, i.e., up to C19 n-alkanes. Each phase gave good recoveries for two test mixtures containing chlorobenzenes and chlorophenols dissolved in 100 μL of water at the 10 ppb level.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Microcolumn Separations 5 (1993), S. 303-315 
    ISSN: 1040-7685
    Keywords: capillary GC ; solid phase extraction ; membrane disks ; water samples ; automation ; nitrogen-phosphorus detection ; mass selective detection ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An automated procedure for the analysis of aqueous samples by membrane disk extraction coupled on-line to capillary gas chromatography (GC) is presented. Organophosphorus pesticides are preconcentrated from aqueous samples on three 0.5 mm thick, 4.0 mm diameter XAD-2 membrane extraction disks which are mounted in a polymer holder for use in a PROSPEKT sample processor. The layers are dried by a stream of nitrogen (30 min at ambient temperature). Desorption of the analytes is carried out with ethyl acetate which is directly introduced into a retention gap under partially concurrent solvent evaporation conditions, using an early solvent vapor exit. The method is a fully software-controlled automated system, and includes sample preparation, sample transfer and GC analysis. The final analysis is carried out by GC with nitrogen-phosphorus (NPD) or mass-selective detection. The technique is applied to the determination of a series of organophosphorus pesticides in tap water and water from European rivers. With a sample volume of only 2.5 mL, the detection limits achieved with the NPD were 20-50 ng L-1 in tap water and 20-100 ng L-1 in river water.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0173-0835
    Keywords: Capillary electrophoresis ; Dialysis ; Sample pretreatment ; Serum ; Sulfonamides ; Urine ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: A fully automated dialysis solid-phase extraction (SPE) sample preparation procedure is coupled on-line to capillary electrophoresis (CE) for the first time. The system is used to determine sulfonamides in serum and urine. The dialysis unit serves to remove proteins and particulate matter. Reconcentration of the analytes is performed with a small SPE column while (in)organic salts and other interferences are removed simultaneously. Finally, the analytes are desorbed and injected, via a homemade interface, into the CE system. Limits of detection (LOD) of 0.05-0.1 and 0.05-0.3 μg/mL are obtained in urine and serum, respectively. The within-day and between-day precisions are in the range of 2-6% and 3-8%, respectively, for a concentration of five times the LOD. The dialysis SPE-CE system was used over a period of six months for the analysis of over 500 serum and urine samples without problems such as clogging of the CE capillary or SPE column.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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