1989
DOI: 10.1016/0045-6535(89)90112-4
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Method 8290: an analytical protocol for the multimedia characterization of polychlorinated dibenzodioxins and dibenzofurans by high-resolution gas chromatography/high-resolution mass spectrometry

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Cited by 24 publications
(21 citation statements)
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“…Nominal detection limits for dioxins and furans were 0.1 ng/g wet weight for eggs except for octaCDD and octaCDF that were 0.3 and 0.2 ng/g; tetraCDD and tetraCDF averaged 0.02 ng/g. The procedure used matrix-specific extraction, analyte-specific cleanup, and high-resolution gas chromatography/high resolution mass spectrometry analysis techniques by a method of internal standard quantitation polychlorinated dibenzo[ p]dioxin using [ 13 C 12 ] polychlorinated dibenzo[ p]dioxin surrogates (Tondeur, 1990;U.S. Environmental Protection Agency, 1990).…”
Section: Chemistrymentioning
confidence: 99%
“…Nominal detection limits for dioxins and furans were 0.1 ng/g wet weight for eggs except for octaCDD and octaCDF that were 0.3 and 0.2 ng/g; tetraCDD and tetraCDF averaged 0.02 ng/g. The procedure used matrix-specific extraction, analyte-specific cleanup, and high-resolution gas chromatography/high resolution mass spectrometry analysis techniques by a method of internal standard quantitation polychlorinated dibenzo[ p]dioxin using [ 13 C 12 ] polychlorinated dibenzo[ p]dioxin surrogates (Tondeur, 1990;U.S. Environmental Protection Agency, 1990).…”
Section: Chemistrymentioning
confidence: 99%
“…Moreover, Supplemental Figs. 5 and 6 demonstrate the absence of analytical detector and sample handling artifacts, and/or chemical interferences susceptible of distorting the congener profiles (Tondeur et al, 1984;Tondeur, 1987). Fig.…”
Section: Resultsmentioning
confidence: 96%
“…We analyzed tissue samples of dosed LE rats (results will be published elsewhere), which were injected on GC/HRMS in a timely manner after the sample preparation, and the recoveries of 13 A serum sample and a solid tissue sample consumed about 63 mL and 131 mL of organic solvents in the sample preparation, respectively. This was only 1/5 of consumption comparing to the conventional methods (6,9). Furthermore, each sample only used 3.2 mL of methylene chloride, a hazardous chlorinated solvent.…”
Section: Resultsmentioning
confidence: 99%