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  • Organochlorine and organophosphorus pesticides  (2)
  • EARTH RESOURCES AND REMOTE SENSING  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Sulfuric acid pretreatment for the simultaneous GC screening of organochlorine and organophosphorus pesticides in herbal essential oils (1998)
    Springer
    Chromatographia 47 (1998), S. 587-592 
    Details
    ISSN: 1612-1112
    Keywords: Gas chromatography ; Organochlorine and organophosphorus pesticides ; Herbal medicine ; Essential oils ; Sulfuric acid treatment
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A rapid and new clean-up method utilizing sulfuric acid treatment is demonstrated to identify and quantify the level of organochlorine (OC) and organophosphorus (OP) pesticide residue concentrations in herbal essential oils by gas chromatography (GC). Essential oils fortified with pesticides, that are extracted from herbs by steam distillation are partitioned with 65% acetonitrile/water(v/v) and treated with sulfuric acid at different reaction times and sulfuric acid concentrations. Optimal conditions, to avoid interference from essential oils in gas chromatographic analysis, is 17% (v/v) of a mixed phase ratio of sulfuric acid to organic solvent (hexane/ethyl ether=9∶1, v/v) and a reaction time of 30s. The response of the flame ionization detector (FID) is linear for all pesticides determined. Recovery of pesticides from fortified herbs studied are in the range of 75% to 111% (RSD, 4% to 11%) for OC, and 72% to 116% (RSD, 2% to 11%) for OP. Although sulfuric acid treatment destroys carbamate and some organophosphorus pesticides, this method has efficiently reduced matrix interference and provides a rapid, economical clean-up method with excellent linear data having low coefficients of variation for the GC analyses of BHC isomers, DDD, DDE, DDT, chlorothalonil, chloropyrifos, tetradifon, fenitrothion, malathion, and parathion in matrices of herbal essential oils.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02467500
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    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Analysis of multi-component pesticide residues in herbal medicines by GC-MS with electron impact ionization and with positive- and negative-ion chemical ionization (1999)
    Springer
    Chromatographia 49 (1999), S. 525-534 
    Details
    ISSN: 1612-1112
    Keywords: Gas chromatography-mass spectrometry ; Organochlorine and organophosphorus pesticides ; Herbal medicines ; Selective-ion monitoring
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary Multicomponent pesticide residues in herbal medicines have been analyzed by gas chromatography-mass spectrometry (GC-MS) with electron impact (EI) ionization and positive- and negative-ion chemical ionization (PCI and NCI). Herbal medicines (5 g) were extracted with 65∶35 (%,v/v) acetonitrile-water, and partitioned with hexane-diethyl ether (1∶1) and hexane-dichloromethane (1∶1). The organic phase of the extracted fraction was cleaned on a Florisil column and analyzed by GC-MS with selected-ion monitoring (SIM). Method detection limits for 27 pesticides were tens of picograms for ECD, NPD and EI-SIM MS, and a few picograms for NCI-SIM MS. The calibration curve for the pesticide standard solution was linear within the range 0.003–30 pg for EI-SIM MS, PCI-SIM MS, and NCI-SIM MS. Mean recoveries of pesticides from spiked herbal medicines (0.75, 1.5, 3 pg) were 61–125% (RSD1–32%) for NCI-SIM MS and 74–121% (RSD 4–12%) for EI-SIM MS. Detection sensitivity and specificity of NCI-SIM MS were better than for ECD and NPD. Parallel use of EI-SIM MS, PCI-SIM MS and NCI-SIM MS was an excellent complementary method for identification and confirmation of multi-component pesticide residues in variety of herbal medicines.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02467753
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    Paper (German National Licenses)
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  • 3
    facet.materialart.
    Unknown
    Atlas of Absorption Lines from 0 to 17900 Cm (sup)-1 (1987)
    In:  CASI
    Details
    Publication Date: 2019-06-28
    Description: Plots of logarithm (base 10) of absorption line strength versus wavenumber from 0 to 17900/cm(sup)-1 are shown for the 28 atmospheric gases (H2O, CO2, O3, N2O, CO, CH4, O2, NO, SO2, NO2, NH3, HNO3, OH, HF, HCl, HBr, HI, ClO, OCS, H2CO, HOCl, N2, HCN, CH3Cl, H2O2, C2H2, C2H6, PH3), which appear in the 1986 Air Force Geophysics Laboratory high-resolution transmission molecular absorption data base (HITRAN) compilation, and for O(P-3), O-18 isotopic ozone, and HO2 from the 1984 JPL compilation in the 0- to 200/cm(sup)-1 region, and infrared solar CO lines at 4500 K. Also shown are plots of logarithm (base 10) of approximate infrared absorption cross sections of 11 heavy molecules versus wavenumber. The cross-section data cover 700 to 1800/cm(sup)-1 and are included as a separate data file in the 1986 HITRAN database.
    Keywords: EARTH RESOURCES AND REMOTE SENSING
    Type: NASA-RP-1188 , L-16330 , NAS 1.61:1188
    Format: application/pdf
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    NASA TECHNICAL REPORTS
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