Lin Wang, Jingjing Guo, Jing Li, Shuwei Pei, Yu Zhang, Zhengke Li, Yalcun Turlana, Xiaohong Zhou and Ruozhen Yu*,
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The iodine-thiosulfate method demonstrated a method detection limit of 0.4 mg L<sup>–1</sup> (<i>n</i> = 7) and a corresponding interlaboratory quantification limit of 1.6 mg L<sup>–1</sup> in water samples with chloride concentrations of 5000 mg L<sup>–1</sup>. The method’s precision and accuracy ranged from 1.4% to 6.7% and −1.0% to 5.0%, respectively. The relative error in permanganate index determination remained below 20% even at chloride concentrations up to 60 g L<sup>–1</sup>, whereas the conventional oxalate-permanganate method exceeded a 20% relative error once the chloride concentration reached 10 g L<sup>–1</sup> or higher. The sufficiently low detection limit along with excellent repeatability (intralaboratory precision), reproducibility (interlaboratory precision), and accuracy confirms its practical feasibility for routine analysis.</p>","PeriodicalId":93847,"journal":{"name":"ACS ES&T water","volume":"5 9","pages":"5395–5404"},"PeriodicalIF":4.3000,"publicationDate":"2025-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Determination of the Permanganate Index in High-Chlorine Water Bodies\",\"authors\":\"Lin Wang, Jingjing Guo, Jing Li, Shuwei Pei, Yu Zhang, Zhengke Li, Yalcun Turlana, Xiaohong Zhou and Ruozhen Yu*, \",\"doi\":\"10.1021/acsestwater.5c00498\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Despite the significant demand, accurate determination of the permanganate index in high-chloride bodies of water remains extremely limited. This study introduces an iodine-thiosulfate method that effectively eliminates the interference of chloride ions in the permanganate index determination. In this method, organic and inorganic substances in a water sample are oxidized with KMnO<sub>4</sub> in an alkaline medium to mitigate chloride ion interference. To further minimize this interference during back-titration, the remaining KMnO<sub>4</sub> is reduced using KI under adjusted acidic conditions. The released iodine is then titrated with standardized Na<sub>2</sub>S<sub>2</sub>O<sub>3</sub> until the starch–iodine complex’s blue–black color disappears. The iodine-thiosulfate method demonstrated a method detection limit of 0.4 mg L<sup>–1</sup> (<i>n</i> = 7) and a corresponding interlaboratory quantification limit of 1.6 mg L<sup>–1</sup> in water samples with chloride concentrations of 5000 mg L<sup>–1</sup>. The method’s precision and accuracy ranged from 1.4% to 6.7% and −1.0% to 5.0%, respectively. The relative error in permanganate index determination remained below 20% even at chloride concentrations up to 60 g L<sup>–1</sup>, whereas the conventional oxalate-permanganate method exceeded a 20% relative error once the chloride concentration reached 10 g L<sup>–1</sup> or higher. 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引用次数: 0
摘要
尽管需求量很大,但在高氯化物水体中准确测定高锰酸盐指数仍然极为有限。本研究介绍了一种有效消除氯离子对高锰酸盐指数测定干扰的硫代硫酸碘法。在该方法中,水样中的有机物和无机物在碱性介质中用KMnO4氧化以减轻氯离子的干扰。为了进一步减少反滴定过程中的干扰,在调整的酸性条件下,使用KI还原剩余的KMnO4。然后用标准的Na2S2O3滴定释放出的碘,直到淀粉-碘复合物的蓝黑色消失。硫代硫酸盐碘法在氯化物浓度为5000 mg L-1的水样中,检测限为0.4 mg L-1 (n = 7),相应的实验室间定量限为1.6 mg L-1。方法精密度和准确度分别为1.4% ~ 6.7%和- 1.0% ~ 5.0%。当氯化物浓度达到60 g L-1时,测定高锰酸盐指数的相对误差仍在20%以下,而传统草酸-高锰酸盐法在氯化物浓度达到10 g L-1或更高时,相对误差超过20%。足够低的检出限以及优异的重复性(实验室内精密度)、再现性(实验室间精密度)和准确性证实了其在常规分析中的实际可行性。
Determination of the Permanganate Index in High-Chlorine Water Bodies
Despite the significant demand, accurate determination of the permanganate index in high-chloride bodies of water remains extremely limited. This study introduces an iodine-thiosulfate method that effectively eliminates the interference of chloride ions in the permanganate index determination. In this method, organic and inorganic substances in a water sample are oxidized with KMnO4 in an alkaline medium to mitigate chloride ion interference. To further minimize this interference during back-titration, the remaining KMnO4 is reduced using KI under adjusted acidic conditions. The released iodine is then titrated with standardized Na2S2O3 until the starch–iodine complex’s blue–black color disappears. The iodine-thiosulfate method demonstrated a method detection limit of 0.4 mg L–1 (n = 7) and a corresponding interlaboratory quantification limit of 1.6 mg L–1 in water samples with chloride concentrations of 5000 mg L–1. The method’s precision and accuracy ranged from 1.4% to 6.7% and −1.0% to 5.0%, respectively. The relative error in permanganate index determination remained below 20% even at chloride concentrations up to 60 g L–1, whereas the conventional oxalate-permanganate method exceeded a 20% relative error once the chloride concentration reached 10 g L–1 or higher. The sufficiently low detection limit along with excellent repeatability (intralaboratory precision), reproducibility (interlaboratory precision), and accuracy confirms its practical feasibility for routine analysis.