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A Rapid Method, Combining Microwave-Assisted Extraction and Gas Chromatography-Mass Spectrometry with a Database, for Determining Organochlorine Pesticides and Polycyclic Aromatic Hydrocarbons in Soils and Sediments
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Citations
17
References
2017
Year
EngineeringPesticide-residue AnalysisRapid MethodChemical ContaminantHexane ExtractEnvironmental ChemistryEnvironmental Analytical ChemistryAnalytical ChemistryPersistent Organic PollutantSoxhlet Extraction MethodSoil ContaminationWater QualityEcotoxicologyPollution SurveysChemical PollutionGas Chromatography-mass SpectrometryEnvironmental EngineeringChemical ContaminantsMass SpectrometryEnvironmental RemediationEnvironmental ToxicologyOrganochlorine PesticidesMedicineDrug Analysis
A rapid method for determining organochlorine pesticides and polycyclic aromatic hydrocarbons in soils and sediments was developed to allow pollution surveys to be performed in emergencies. The method involves microwave-assisted extraction and uses an automated identification/quantification system with a gas chromatography mass spectrometry database. A sample (3 g) is extracted with a 3:2 v/v hexane:water mixture (10 mL) for 30 min using a microwave-assisted extraction system at 120°C. The hexane extract is then cleaned using silica gel, then analyzed by gas chromatography mass spectrometry. The total analysis time is approximately 4 h. The precision of the quantitative results and accuracy of the analyte identification were determined. The total analyte concentrations were generally comparable to (61%–110% of) the concentrations determined using a Soxhlet extraction method, but the concentrations of individual high-molecular-weight polycyclic aromatic hydrocarbons were unacceptably low compared with the concentrations determined using the Soxhlet method. However, these compounds (e.g., benzo(ghi)perylene and indeno(1,2,3-cd)pyrene) were subsequently efficiently extracted using a hexane:water:ethanol mixture. The accuracy of identification was evaluated using accurate masses determined by gas chromatography time-of-flight mass spectrometry, and the mass error was 2 ppm for 21 of the 22 compounds identified using the new method.
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