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使用便于介质交换的复合电极系统在铋膜电极上通过吸附溶出伏安法测定铟。

Determination of indium by adsorptive stripping voltammetry at the bismuth film electrode using combined electrode system facilitating medium exchange.

作者信息

Martynov Leonid Yu, Sadova Maria K, Sakharov Konstantin A, Yashtulov Nikolai A, Zaytsev Nikolay K

机构信息

Lomonosov Institute of Fine Chemical Technologies, MIREA - Russian Technological University, 86 Vernadsky Avenue, Moscow 119454, Russia.

Lomonosov Institute of Fine Chemical Technologies, MIREA - Russian Technological University, 86 Vernadsky Avenue, Moscow 119454, Russia.

出版信息

Talanta. 2024 May 1;271:125680. doi: 10.1016/j.talanta.2024.125680. Epub 2024 Jan 16.

Abstract

A novel method of determining indium has been described in this article which uses adsorptive stripping voltammetry (AdSV) and 4-(2-pyridylazo)-resorcinol (PAR) as a chelating agent or as the preconcentration agent. The measurements were performed using square-wave voltammetry by using a combined electrode system, which allows for preconcentration and stripping without opening the circuit. Ex situ plated bismuth film electrode (BiFE) was used as the working electrode. A potential-time program was developed for the inversion cycle stages based on the various factors that affect the magnitude of the inversion signal. The calibration curve was linear in a concentration range of 2·10 to 4·10 М when the pH is 4.8, accumulation potential is -700 mV, and PAR concentration is 1·10 M. The detection limit for the 3σ criterion with an accumulation time of 120 s was 3.5·10 М. Several interferences caused by Tl(I), Zn(II), Cu(II), Pb(II), Co(II), Ni(II), Mn(II), Fe(III), Cr(III) ions have been studied, and it has been shown that medium exchange procedure can effectively eliminate some interferences. It was demonstrated that the method can be applied to the determination of indium in tap water and in ITO glass sample.

摘要

本文描述了一种测定铟的新方法,该方法使用吸附溶出伏安法(AdSV)和4-(2-吡啶偶氮)-间苯二酚(PAR)作为螯合剂或预富集剂。测量采用方波伏安法,使用组合电极系统,无需断开电路即可进行预富集和溶出。异位镀铋膜电极(BiFE)用作工作电极。基于影响反转信号大小的各种因素,为反转循环阶段开发了一个电位-时间程序。当pH值为4.8、富集电位为-700 mV且PAR浓度为1·10⁻⁵ M时,校准曲线在2·10⁻⁸至4·10⁻⁸ М的浓度范围内呈线性。在120 s的富集时间下,3σ标准的检测限为3.5·10⁻⁸ М。研究了由Tl(I)、Zn(II)、Cu(II)、Pb(II)、Co(II)、Ni(II)、Mn(II)、Fe(III)、Cr(III)离子引起的几种干扰,结果表明,介质交换程序可以有效消除一些干扰。结果表明,该方法可用于自来水和ITO玻璃样品中铟的测定。

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