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The presence of the pesticide ethion was determined using an electroanalytical method, i.e., linear sweep stripping voltammetry at a hanging mercury drop electrode in the Britton-Robbinson buffer with pH=8.36, based on its reduction peak observed at -690 mV following its alkaline hydrolysis. The experimental parameters, namely, the preconcentration potential, the preconcentration time, and the scan rate were investigated and -300 mV(vs. Ag/AgCl), 270 s, and 100 mV/s were selected as the optimal values, respectively. The linear relationship between the peak current and the concentration was found to be in the range of 0.02_0.16 mg/L, with a detection limit of 0.0087 mg/L. The proposed method was applied to the determination of ethion in spiked vegetable and fruit samples via a preextraction with anhydrous ethanol.
The presence of the pesticide ethion was determined using an electroanalytical method, ie, linear sweep stripping voltammetry at a hanging mercury drop electrode in the Britton-Robbinson buffer with pH = 8.36, based on its reduction peak observed at -690 mV following its alkaline hydrolysis . The experimental parameters, namely, the preconcentration potential, the preconcentration time, and the scan rate were investigated and -300 mV (vs. Ag / AgCl), 270 s, and 100 mV / s were selected as the optimal values, respectively. The linear relationship between the peak current and the concentration was found to be in the range of 0.02 - 0.16 mg / L with a detection limit of 0.0087 mg / L. The proposed method was applied to the determination of ethion in spiked vegetable and fruit samples via a preextraction with anhydrous ethanol.