Electrochemical interference study of manganese and iron by multiplex method and the application for manganese analysis in drinking water

IF 2.9 Q2 ELECTROCHEMISTRY
Yichun Shi, Yu Pei, Nicholas Lamothe, Kirsten Macdonald, Sarah Jane Payne, Zhe She
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Abstract

Manganese is an emerging concern in drinking water, due to its potential health and aesthetic effects. Although accurate and sensitive, spectroscopic techniques for Mn2+ detection are costly and not capable of rapid detection. Electrochemical methods, such as cathodic stripping voltammetry, have been intensively explored as portable low-cost methods for Mn2+ detection. Challenges of reliability and matrix interference are difficult to overcome with current electrochemical methods. Among the interference reagents, Fe2+ is one of the biggest challenges for Mn2+ detection. Herein, a new method based on multiplex chronoamperometry at potentials between 0.9 and 1.4 V by a multichannel potentiostat is explored for its ability for interference resistance and applicability for Mn2+ detection in real drinking water samples. Compared to conventional one-channel electrochemical techniques, the multiplex method generates a reliable pattern that is unique to the sample components. The interference between Mn2+ and Fe2+ is investigated and the results are promising even at 100:1 Fe2+:Mn2+ concentrations. The detection limit determined for the multiplex method was 25.3 μM, and the optimum recovery rate in a real drinking water sample was 99.8%.

Abstract Image

多重法对锰和铁的电化学干扰研究及在饮用水中锰分析中的应用
由于锰对健康和美观的潜在影响,锰正在成为饮用水中的一个新问题。用于检测 Mn2+ 的光谱技术虽然准确灵敏,但成本高昂,而且不能快速检测。阴极剥离伏安法等电化学方法作为便携式、低成本的 Mn2+ 检测方法受到了广泛关注。目前的电化学方法难以克服可靠性和基质干扰的挑战。在干扰试剂中,Fe2+ 是 Mn2+ 检测面临的最大挑战之一。在此,我们探讨了一种基于多通道恒电位仪在 0.9 至 1.4 V 电位下进行多重时变测量的新方法,以确定其抗干扰能力和在实际饮用水样品中检测 Mn2+ 的适用性。与传统的单通道电化学技术相比,多通道方法能产生可靠的样品成分特有模式。对 Mn2+ 和 Fe2+ 之间的干扰进行了研究,即使在 Fe2+:Mn2+ 浓度为 100:1 的情况下,结果也很乐观。多重方法的检测限为 25.3 μM,在实际饮用水样品中的最佳回收率为 99.8%。
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来源期刊
CiteScore
3.80
自引率
0.00%
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审稿时长
10 weeks
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