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Differential pulse voltammetric determination of 4-nitroaniline using a glassy carbon electrode: comparative study between cathodic and anodic quantification

机译:玻碳电极差分脉冲伏安法测定4-硝基苯胺:阴极和阳极定量的比较研究

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摘要

Differential pulse voltammetry with a glassy carbon electrode was used for the determination of trace amounts of 4-nitroaniline in Britton-Robinson buffer at pH 2.0 as an optimal base electrolyte. 4-Nitroaniline can be determined by differential pulse voltammetry directly using either its electrochemical oxidation or reduction. The calibration curve was measured for both reactions in the same concentration range from 2 to 100 mu mol dm(-3). The calculated limits of detection and quantification are 0.2 and 0.7 mu mol dm(-3) (RSD 6.62 % and R (2) = 0.9906 for n = 5) for cathodic reduction and 0.3 and 1.0 mu mol dm(-3) (RSD 7.62 % and R (2) = 0.9995 for n = 5) for anodic oxidation.
机译:使用玻璃碳电极的差示脉冲伏安法测定了在Britton-Robinson缓冲液中作为最佳基础电解质的痕量4-硝基苯胺在pH 2.0下的情况。 4-硝基苯胺可通过差示脉冲伏安法直接使用其电化学氧化法或还原法测定。在2至100μmoldm(-3)的相同浓度范围内,对两个反应均测量了校准曲线。阴极还原的计算检出限和定量限分别为0.2和0.7μmol dm(-3)(RSD 6.62%和R(2)= 0.9906(n = 5))(0.3和1.0μmol dm(-3)(RSD)对于阳极氧化,为7.62%,对于n = 5,R(2)= 0.9995。

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