Yichun Shi, Yu Pei, Nicholas Lamothe, Kirsten Macdonald, Sarah Jane Payne, Zhe She
{"title":"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","authors":"Yichun Shi, Yu Pei, Nicholas Lamothe, Kirsten Macdonald, Sarah Jane Payne, Zhe She","doi":"10.1002/elsa.202300011","DOIUrl":null,"url":null,"abstract":"<p>Manganese is an emerging concern in drinking water, due to its potential health and aesthetic effects. Although accurate and sensitive, spectroscopic techniques for Mn<sup>2+</sup> 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 Mn<sup>2+</sup> detection. Challenges of reliability and matrix interference are difficult to overcome with current electrochemical methods. Among the interference reagents, Fe<sup>2+</sup> is one of the biggest challenges for Mn<sup>2+</sup> 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 Mn<sup>2+</sup> 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 Mn<sup>2+</sup> and Fe<sup>2+</sup> is investigated and the results are promising even at 100:1 Fe<sup>2+</sup>:Mn<sup>2+</sup> 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%.</p>","PeriodicalId":93746,"journal":{"name":"Electrochemical science advances","volume":null,"pages":null},"PeriodicalIF":2.9000,"publicationDate":"2023-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/elsa.202300011","citationCount":"0","resultStr":"{\"title\":\"Electrochemical interference study of manganese and iron by multiplex method and the application for manganese analysis in drinking water\",\"authors\":\"Yichun Shi, Yu Pei, Nicholas Lamothe, Kirsten Macdonald, Sarah Jane Payne, Zhe She\",\"doi\":\"10.1002/elsa.202300011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Manganese is an emerging concern in drinking water, due to its potential health and aesthetic effects. Although accurate and sensitive, spectroscopic techniques for Mn<sup>2+</sup> 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 Mn<sup>2+</sup> detection. Challenges of reliability and matrix interference are difficult to overcome with current electrochemical methods. Among the interference reagents, Fe<sup>2+</sup> is one of the biggest challenges for Mn<sup>2+</sup> 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 Mn<sup>2+</sup> 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 Mn<sup>2+</sup> and Fe<sup>2+</sup> is investigated and the results are promising even at 100:1 Fe<sup>2+</sup>:Mn<sup>2+</sup> 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%.</p>\",\"PeriodicalId\":93746,\"journal\":{\"name\":\"Electrochemical science advances\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2023-06-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/elsa.202300011\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Electrochemical science advances\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/elsa.202300011\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"ELECTROCHEMISTRY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Electrochemical science advances","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/elsa.202300011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
Electrochemical interference study of manganese and iron by multiplex method and the application for manganese analysis in drinking water
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%.