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GC Determination of Residual Organophosphorus Pesticides in Hangzhou White Chrysanthemum by Treatment of Samples with Single Extractant

Wang Xuan-zheng

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Abstract

Residual amounts of organophosphorus pesticides in samples of Hangzhou white chrysanthemum were extracted with acetone singly,and the extract obtained were purified by the CARB/NH2 SPE column.Eluate from the column was concentrated to 1-2 mL by rotary evaporation at 30 ℃ and then to ca.0.4 mL by N2-blowing.After making up to 0.5 mL,the solution in acetone was used for GC determination.By using the DB-1701 quartz capillary chromatographic column,8 organophosphorus pesticides were separated and determined by NPD.Ranges of linearity of the working curves for these 8 pesticides were kept within 5.0 mg·L-1,and the values of detection limit(3S/N) found were in the range of 0.009-0.028 μg·g-1.Precision and recovery of the method were tested,and values of RSD′s(n=6) and of recovery found were in the ranges of 5.45%-7.27% and 67.3%-104.0% respectively.

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What this paper is about

Residual amounts of organophosphorus pesticides in samples of Hangzhou white chrysanthemum were extracted with acetone singly,and the extract obtained were purified by the CARB/NH2 SPE column.Eluate from the column was concentrated to 1-2 mL by rotary evaporation at 30 ℃ and then to ca.0.4 mL by N2-blowing.After making up to 0.5 mL,the solution in acetone was used for GC determination.By using the DB-1701 quartz capillary chromatographic column,8 organophosphorus pesticides were separated and determined by NPD.Ranges of linearity of the working curves for these 8 pesticides were kept within 5.0 mg·L-1,and the values of detection limit(3S/N) found were in the range of 0.009-0.028 μg·g-1.Precision and recovery of the method were tested,and values of RSD′s(n=6) and of recovery found were in the ranges of 5.45%-7.27% and 67.3%-104.0% respectively.

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Available abstract

Residual amounts of organophosphorus pesticides in samples of Hangzhou white chrysanthemum were extracted with acetone singly,and the extract obtained were purified by the CARB/NH2 SPE column.Eluate from the column was concentrated to 1-2 mL by rotary evaporation at 30 ℃ and then to ca.0.4 mL by N2-blowing.After making up to 0.5 mL,the solution in acetone was used for GC determination.By using the DB-1701 quartz capillary chromatographic column,8 organophosphorus pesticides were separated and determined by NPD.Ranges of linearity of the working curves for these 8 pesticides were kept within 5.0 mg·L-1,and the values of detection limit(3S/N) found were in the range of 0.009-0.028 μg·g-1.Precision and recovery of the method were tested,and values of RSD′s(n=6) and of recovery found were in the ranges of 5.45%-7.27% and 67.3%-104.0% respectively.

Key concepts: Chromatography, Acetone, Chemistry, Detection limit, Pesticide, Elution, Extraction (chemistry), Pesticide residue

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