International Journal of Environmental & Analytical Chemistry · 2013 · 46 citations · 43 references
Solvent ExtractionPrecision AgricultureEngineeringPesticide-residue AnalysisPrecision Crop ProtectionSubstrates LinearityEnvironmental ChemistryBiorational PesticideEnvironmental Analytical ChemistryAnalytical ChemistryInsecticideChromatographyWater QualityPest ManagementEcotoxicologyEnergy Crop PesticidesRape PlantRape Plant MatricesEnvironmental EngineeringCrop ProtectionMass SpectrometryEnvironmental RemediationEnvironmental ToxicologyMedicineRunoff Water MatricesDrug Analysis
QuEChERS and solid phase extraction (SPE) methods were applied for determining four herbicides (metazachlor, oxyfluorfen, quizalofop-p-ethyl, quinmerac) and one insecticide (α(±)-cypermethrin) in runoff water, soil, sunflower and oilseed rape plant matrices. Determination was performed using gas chromatography mass spectrometry (GC-MS), whereas high-pressure liquid chromatography mass spectrometry (HPLC-MS) was used for quinmerac. In all substrates linearity was evaluated using matrix-matched calibration samples at five concentration levels (50–1000 ng L−1 for water, 5–500 μg kg−1 for soil and 2.5–500 μg kg−1 for sunflower or oilseed rape plant). Correlation coefficient was higher than 0.992 for all pesticides in all substrates. Acceptable mean recovery values were obtained for all pesticides in water (65.4–108.8%), soil (70.0–110.0%) and plant (66.1–118.6%), with intra- and inter-day RSD% below 20%. LODs were in the range of 0.250–26.6 ng L−1 for water, 0.10–1.8 μg kg−1 for soil and 0.15–2.0 μg kg−1 for plants. The methods can be efficiently applied for field dissipation studies of the pesticides in energy crop cultivations.
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Michelangelo Anastassiades, Steven J. Lehotay, Darinka Štajnbaher et al. · Journal of AOAC International · 2003 · 5.4K citations
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Residue (Chemistry), Engineering, Pesticide-residue Analysis +10