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  • 1
    ISSN: 1432-1130
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract In the development of a screening method for the determination of residues of mecoprop in soils involving coupled-column RPLC-UV (228 nm) the cleanup performance of a 5 μm GFF-II internal surface reversed phase (ISRP, Pinkerton) analytical column (50 × 4.6 mm I.D.) as a first column was investigated. In comparison to an analytical C18 column the ISRP column substantially improved the separation between acidic analyte and co-extracted humic substances. Under the selected coupled-column conditions soil extracts obtained after hydrolysis with an aqueous alkaline solution, acidifying and centrifugation could be analyzed directly allowing the determination of mecoprop in soils to a level of about 0.02 mg/kg. A rapid concentration step on a 100 mg C18 solid phase extraction (SPE) cartridge was adopted into the procedure providing a limit of detection (S/N = 3) of 0.01 mg/kg of mecoprop in soil. The method was validated by analyzing freshly spiked soil samples and samples with aged residues. In case of freshly spiked samples the overall recovery was 87% (n = 18, spiked level 0.02–8.0 mg/kg) with a repeatability of 6.8% and a reproducibility of 8.3%. No significant decrease of the recovery was observed for samples with aged residues (n = 15, spiked level 0.1 and 8.0 mg/kg) during a storage of 29 days in the refrigerator at about 4 °C; a storage of 67 days provided a mean recovery of 76% (n = 14, spiked level 8.0 mg/kg).
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Microwave-assistend solvent extraction (MASE) ; Pesticide residue analysis ; Triazine herbicides ; Soil samples
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The use of microwave-assisted solvent extraction (MASE) as an alternative for conventional solvent extraction procedures for the determination of some triazine herbicides in soil samples has been investigated. In this study MASE method development was focused on the selection of a suitable extraction solvent prior to the instrumental analysis of uncleaned extracts with gas chromatography and nitrogen-specific detection. A mixture of dichloromethane-methanol (90∶10, v/v) yielded recoveries ranging from 89 to 103 (spiked level 200 μg/kg) with RSDs ranging from 2.1 to 5.3%. This solvent mixture is also very convenient for further procedure. The selected MASE procedure was tested by analyzing freshly spiked soil samples and samples with aged residues of atrazine, desethylatrazine, desisopropylatrazine and simazine. The results were compared with those obtained by a conventional liquid extraction method. The comparative study indicated that MASE yields recoveries at least as good as those obtained by the conventional method. Moreover, the MASE procedure provides low solvent consumption in combination with a high sample throughput.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1612-1112
    Keywords: Column liquid chromatography ; Column switching ; Step-gradient elution ; Optimization ; Trace analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A computer spreadsheet application has been developed for the optimization of step-gradient elution conditions as applied in coupled-column RPLC for online clean-up and separation in the analysis of pesticide residues. The procedure is based on the experimentally determined retention behaviour of the analytes as a function of mobile phase composition. Retention and peak volumes of the analytes eluting under isocratic and one- and/or two-step gradient conditions can be calculated. For a given set of analytes, the spreadsheet systematically calculates the resolution of the least efficiently separated pair of peaks in the space defined by the eluotropic strengths of the mobile phases and the time at which the step-gradient takes place. The performance of the proposed procedure was tested and evaluated for the analysis of nine polar pesticides for which in a previous study adequate conditions had been found by computer-aided chromatogram simulation. the optimum conditions predicted by the procedure were in good agreement with those established experimentally and by simulation. The simultaneous production of data on retention, peak volume and resolution for a group of analytes under selected one- and/or two step-gradient elution conditions makes the calculation procedure highly productive and flexible in searching for and/or adjusting appropriate separation conditions.
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  • 4
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Soil samples ; Microwave-assisted solvent extraction ; Nitrogen detection ; Triazine herbicides
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Recent work demonstrated that the combination of microwave assisted solvent extraction (MASE) and capillary gas chromatography with selective nitrogen detection (GC-NPD) is a viable approach for the efficient determination of triazine herbicides in soils. However, for soils with a high organic matter content or the injection of more concentrated extracts to obtain lower LOD's the performance of gas chromatographic analysis of uncleaned extracts is hampered. This results in both a decrease of the chromatographic response of analytes and a decrease in the life time of the column due to coextracted matrix substances. The effect of various types of soils on the chromatographic analysis of triazine herbicides was studied. It appeared that for the investigated samples with an organic matter content below 5% processing of uncleaned extracts is possible. Samples with a higher organic matter content required a cleanup step. A rapid procedure on 100 mg silica cartridges has been developed using solvents compatible with the MASE extracts and the instrumental analysis. Beside the testing with different standard soils, about 120 samples of an ongoing monitoring program involving three different types of soil (organic matter content: 3–37%) were analysed. The selected compounds atrazine, desethylatrazine, desisopropyl-atrazine and simazine could be assayed in the various soil types to a level of at least 2 μg kg−1. For soil samples with a high organic matter content (〉5%), the rapid cleanup procedure allowed the trace analysis of the triazines and considerably increased the life time of the capillary column. Recoveries at levels from 2 to 50 μg kg−1 ranged from 70 to 100% with RSDs ranging from 5.1 to 9.5%. Confirmation of positive samples was carried out by gas chromatography mass spectrometry.
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  • 5
    ISSN: 1612-1112
    Keywords: Colum liquid chromatography ; Ethylenethiourea in ground water ; Column switching ; Trace analysis ; Screening for ETU
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Column-switching with two C18 separation columns combined with UV detection at 233 nm has been used to determine ETU in ground water samples. The direct assay of ETU (limit of detection, 1 ppb) takes less than 10 min. For the determination of ETU down to a level of 0.1 ppb, preconcentration of ETU is achieved by a liquid-liquid extraction procedure allowing the analysis of at least 12 water samples per day. For both methods (1-ppb and 0.1-ppb level), the overall recovery (96 and 82%), the repeatability (4.5 and 4.3%) and the reproducibility (5.0 and 7.9%) are satisfactory (n=18 and 28, respectively). More than one hundred samples of ground water were analysed during a 10-month period; over 0.1 ppb of ETU (range, 0.1–300 ppb) was found in 30% of the samples tested.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 339 (1991), S. 348-356 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary An overview is given of the applicability of HPLC with column-switching in pesticide residue analysis. The main advantage of HPLC with column-switching is the enhancement of both sensitivity and selectivity combined with a high potential for automation. The selection of optimal conditions such as column dimensions, mobile phase compositions and multi step gradient elution is discussed.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 343 (1992), S. 73-74 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 12 (1989), S. 784-789 
    ISSN: 0935-6304
    Keywords: Normal phase HPLC ; Column switching ; Automated analysis ; Organochlorine pesticides ; Polychlorinated biphenyls ; Human milk ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method has been developed for the automated sample pretreatment of organochlorine pesticides (OCP's) and polychlorinated biphenyls (PCB's) in extracts of human milk. This work was part of a regular monitoring program presently carried out at our institute. In this program several hundreds of human milk samples have to be analyzed for the occurrence of PCB's and OCP's.With a normal bore straight phase HPLC system, utilizing column switching we are able to separate the fat from the compounds of interest and, moreover, complete separation of the PCB fraction from the OCP's can be achieved. Under the conditions used to separate the PCB fraction from intefering OCP's column-switching is essential since the retention times for the OCP's vary from 4 minutes for hexachlorobenzene (HCB) to more than 2 hours for dieldrin.1 ml of an extract containing 45 mg of fat is injected on the first (pre)column, the fat is retained on this column and the early eluting HCB, the PCB fraction, and the DDT complex are transferred to the second (analytical) column. Compounds eluting later than p,p′-DDT are collected directly from the precolumn. Meanwhile, the PCB fraction is separated from the rest of the OCP's on the analytical column.Contrary to conventional gravity-controlled chromatography or solid phase extraction the clean-up process can be monitored on-line by UV-detection, thus rendering a fast and reliable optimization of the system. The OCP-fractions collected from the LC are pooled before they are transferred to a high resolution gas chromatograph equipped with a large volume option. The PCB-fraction is injected directly in a HRGC equipped with a concurrent solvent evaporation injection device.The limits of detection for the OCP's (HCB, α-,β- and γ-HCH, β-Hepo (heptachlorepoxide), dieldrin, p,p′-DDE, o,p′-DDT p,p′-DDT and TDE) and the PCB's investigated are at sub-ppb level (fat basis); the recoveries vary from 80 to 100%.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Publication Date: 1998-09-01
    Print ISSN: 0009-5893
    Electronic ISSN: 1612-1112
    Topics: Chemistry and Pharmacology
    Published by Springer
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  • 10
    Publication Date: 1996-11-01
    Print ISSN: 0009-5893
    Electronic ISSN: 1612-1112
    Topics: Chemistry and Pharmacology
    Published by Springer
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