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基于氧化铱纳米粒子修饰玻碳电极的高灵敏度和选择性安培传感器用于检测纳摩尔级的碘酸盐和高碘酸盐。

Highly sensitive and selective amperometric sensors for nanomolar detection of iodate and periodate based on glassy carbon electrode modified with iridium oxide nanoparticles.

机构信息

Department of Chemistry, University of Kurdistan, P.O. Box 416, Sanandaj, Iran.

出版信息

Anal Chim Acta. 2010 Feb 19;661(1):28-34. doi: 10.1016/j.aca.2009.12.005. Epub 2009 Dec 16.

Abstract

Iridium oxide nanoparticles are grown on a glassy carbon electrode by electrodepositing method. The electrochemical behavior and electrocatalytic activity of modified electrode towards reduction of iodate and periodate are studied. The reductions of both ions occur at the unusual positive peak potential of 0.7 V vs. reference electrode. The modified electrode is employed successfully for iodate and periodates detection using cyclic voltammetry, hydrodynamic amperometry and flow injection analysis (FIA). In the performed experiments, flow injection amperometric determination of iodate and periodate yielded calibration curves with the following characteristics: linear dynamic range up to 100 and 80 microM, sensitivity of 140.9 and 150.6 nA microM(-1) and detection limits of 5 and 36 nM, respectively. The repeatability of the modified electrode for 21 injections of 1.5 microM of iodate solution is 1.5%. The interference effects of NO(2)(-), NO(3)(-), ClO(3)(-), BrO(3)(-), ClO(4)(-), SO(4)(2-), Cu(2+), Zn(2+), Mn(2+), Mg(2+), Cd(2+), Ca(2+), Na(+), K(+), NH(4)(+) and K(+), CH(3)COO(-) and glucose were negligible at the concentration ratio of more than 1000. The obtained attractive analytical performance together with high selectivity and simplicity of the proposed method provide an effective and e novel modified electrode to develop an iodate and periodate sensor. Sensitivity, selectivity, the liner concentration range and the detection limit of the developed sensor are all much better than all known similar sensors in the literature for iodate and periodate determination.

摘要

氧化铱纳米粒子通过电沉积方法生长在玻碳电极上。研究了修饰电极对碘酸盐和高碘酸盐还原的电化学行为和电催化活性。两种离子的还原都发生在异常正的 0.7 V 对参比电极的峰电位。采用循环伏安法、动态安培法和流动注射分析(FIA)成功地将修饰电极用于碘酸盐和高碘酸盐的检测。在进行的实验中,碘酸盐和高碘酸盐的流动注射安培法测定得到了以下特征的校准曲线:线性动态范围高达 100 和 80 microM,灵敏度分别为 140.9 和 150.6 nA microM(-1),检测限分别为 5 和 36 nM。修饰电极对 21 次 1.5 microM 碘酸盐溶液的重复性能为 1.5%。在浓度比大于 1000 时,NO(2)(-)、NO(3)(-)、ClO(3)(-)、BrO(3)(-)、ClO(4)(-)、SO(4)(2-)、Cu(2+)、Zn(2+)、Mn(2+)、Mg(2+)、Cd(2+)、Ca(2+)、Na(+)、K(+)、NH(4)(+)和 K(+)、CH(3)COO(-)和葡萄糖对修饰电极的干扰可以忽略不计。该方法具有高选择性和简单性,获得了有吸引力的分析性能,为开发碘酸盐和高碘酸盐传感器提供了一种有效而新颖的修饰电极。与文献中所有已知的类似传感器相比,所开发传感器的灵敏度、选择性、线性浓度范围和检测限都要好得多。

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