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Interference Free Simultaneous Detection of Dihydroxy Benzene Isomers at Cost-effective and Reliable Celestine Blue Modified Glassy Carbon Electrode

机译:在成本效益且可靠的Celestine Blue Modified Glassy碳电极上,双羟基异构体的干扰同时检测二羟基异构体

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摘要

A successful cyclic voltammetric electropolymerisation and electrochemical characterization of celestine blue (CB) was achieved on glassy carbon electrode (GCE). The fabricated electrode was then used for the electroanalysis of hydro- quinone (HQ) and catechol (CC). Due to the improved electro- catalytic activity of the fabricated electrode, an interference free simultaneous detection of CC by HQ was observed. The scan rate studies suggest the diffusion-controlled kinetics phenomenon at the modified electrode. Concentration studies, yielding a limit of detection (LoD) of 0.0491 μM and 0.0456 μM for CC and HQ respectively in the first linear range of 0 to 40 μM, limit of detection of 0.0621 μM and 0.0638 μM for CC and HQ respectively in the second linear range of 50 to 120 μM, which were relatively lower as compared to previous reports was achieved by using differential pulse voltammetry (DPV). In order to evaluate the analytical performance of the CB/GCE, tap water sample analysis was carried out and good recovery results were obtained.
机译:在玻璃碳电极(GCE)上实现了Celestine Blue(CB)的成功循环伏安电化和电化学表征。然后将制造的电极用于羟基酮(HQ)和儿茶酚(CC)的电分析。由于制造的电极的电催化活性的改善,观察到HQ对CC进行干扰的同时检测。扫描速率研究表明,修饰电极处的扩散控制动力学现象。浓度研究,在0至40μM的第一个线性范围内,CC和HQ分别得出0.0491μm和0.0456μm的检测限(LOD),CC分别为0.0621μm和0.0621μm和0.0638μm的检测极限。通过使用差分脉冲伏安法(DPV)实现了50至120μM的线性范围,相比之下,与先前的报道相比相对较低。为了评估CB/GCE的分析性能,进行了自来水样品分析并获得了良好的恢复结果。

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