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A simple voltammetric determination of metsulfuron-methyl in water samples using differential pulse cathodic stripping voltammetry

机译:差分脉冲阴极溶出伏安法简单测定伏安法中的甲磺隆

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摘要

The voltammetric determination of metsulfuron-methyl, a type of pesticide, was investigated on a hanging mercury drop electrode using a differential pulse cathodic stripping voltammetry technique. The experimental parameters, such as the pH of the Britton–Robinson buffer, accumulation time, accumulation potential and initial potential were optimized for the metsulfuron-methyl determination. A well-defined reduction peak was observed at pH 2.0 to 4.0 in the potential range of −0.75 to −1.0 V. The pH of 2.0 was chosen as the optimum pH due to a good stripping signal of the reduction peak. There were no significant interfering ion effects on the electroanalysis of metsulfuron-methyl. The optimized parameters were then used to determine metsulfuron-methyl in the commercial pesticide Ally. The proposed method was highly sensitive due to the lower limit of determination (0.04 mg/L), being relatively selective, and consisting of good precision. The recovery values achieved were about 93% in water samples for this analysis.
机译:使用差分脉冲阴极溶出伏安法,在悬挂的汞滴电极上研究了甲草隆甲磺隆的农药伏安测定。实验参数,例如Br​​itton-Robinson缓冲液的pH,累积时间,累积电势和初始电势已针对甲磺隆的甲基化进行了优化。在pH值为2.0至4.0时,在-0.75至-1.0 V的电位范围内观察到一个明确定义的还原峰;由于还原峰的汽提信号良好,因此选择2.0的pH作为最佳pH。对甲磺隆的电分析没有明显的干扰离子影响。然后将优化的参数用于测定商品农药Ally中的甲磺隆甲基。该方法的测定下限为0.04μg/ L,具有较高的灵敏度,相对选择性和较高的精密度。对于该分析,在水样中获得的回收率约为93%。

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