聚铬蓝黑R修饰碳糊电极上Hg2+的电化学测定

Abdoulkadri Ayouba Mahamane, Abdoulaye Idrissa Kalidou, Hassane Adamou, Bachir Mijitaba Sahirou, A. Walcarius, R. Adamou
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摘要

本文提出了一种新的、简单、快速、高效的测定无机汞(Hg2+)的电化学方法——差分脉冲阳极溶出伏安法(DPASV)。首先,通过循环伏安法和电化学阻抗谱法研究了Hg2+在改性电极上的行为,以评估其性能并了解其表面发生的现象。然后使用DPASV在HClO4介质中优化传感器。优化后,在1 × 10-9 ~ 9 × 10-9 mol.L-1浓度范围内得到线性校准图,相关系数R2= 0.9975%,检出限(LOD)和定量限(LOQ)分别为3.23 × 10-10 mol.L-1和1.07 × 10-9 mol.L-1。7次测量的相对标准偏差(RSD)为3.07%,证明该传感器重复性好。最后,将该方法成功应用于实际水样中,得到了满意的结果,Hg2+的回收率在99.2% ~ 100.1%之间。
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Electrochemical Determination of Hg2+ on a Poly (Eriochrome Blue Black R) Modified Carbon Paste Electrode
In this work a new, simple, fast, and efficient electrochemical approach for the determination of inorganic mercury (Hg2+) using the differential pulse anodic stripping voltammetry (DPASV) technique was presented. This is achieved by modifying the surface of a carbon paste electrode by electropolymerization of Eriochrome blue black R. First, the behavior of Hg2+ on the modified electrode is studied by cyclic voltammetry and electrochemical impedance spectroscopy, to evaluate performance and understand the phenomena that take place on its surface. DPASV is then used to optimize the sensor in HClO4 medium. After optimization, a linear calibration graph was obtained in the concentration range of 1x10-9 to 9x10-9 mol.L-1 with correlation coefficient R2= 0.9975%, the limit of detection (LOD) and the limit of quantification (LOQ) obtained are respectively 3.23x10-10 mol.L-1 and 1.07x10-9 mol.L-1. The relative standard deviation (RSD) for 7 measurements is 3.07%, which proves that this sensor is reproducible. Finally, this method has been successfully applied in real samples of water and the results obtained are satisfactory because the recovery rates of Hg2+ vary from 99.2 to 100.1%.
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