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

IF 2.9 Q2 ELECTROCHEMISTRY Electrochemical science advances Pub Date : 2023-06-08 DOI:10.1002/elsa.202300011
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%.

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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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CiteScore
3.80
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审稿时长
10 weeks
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