Solid-phase spectrophotometric determination of hydrogen peroxide

Q4 Chemistry Analitika i Kontrol Pub Date : 2019-01-01 DOI:10.15826/ANALITIKA.2019.23.2.010
N. Gavrilenko, N. V. Saranchina, D. A. Fedan, M. Gavrilenko
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Abstract

A combined solid-phase spectrophotometric iodometric method for the determination of hydrogen peroxide using a methacrylate polymer was proposed. The method was based on the oxidation reaction of iodide ion with hydrogen peroxide in the hydrochloric acid with the release of free iodine. The iodine was extracted from the solution by a polymethacrylate matrix, and its concentration was measured at the absorbance of 365 nm. The amount of iodine extracted by the polymethacrylate matrix was proportional to the concentration of hydrogen peroxide in the solution. The effect of interfering ions was also investigated. The optimal phase contact time was 5 minutes. The effect of adding the hydrochloric acid to the analyzed solution on the analytical signal of the polymethacrylate matrix after its contact with hydrogen peroxide solution was studied. It was shown that the maximum signal was obtained in the range of acid concentrations in the solution of (3–5)∙10 –3 M. The optimal concentration of potassium iodide in the analyzed solution for the redox reaction was 0.06%. At this concentration, the widest range of detectable concentrations was achieved with the smallest limit of detection for hydrogen peroxide. The developed procedure ensured the determination in the range of (15–130)∙10 -5 % of hydrogen peroxide with the detection limit of 5 × 10 -5 %. The results of the determination of hydrogen peroxide were given for the proposed method in samples of disinfectants and bleaching agents. The proposed method for hydrogen peroxide determination is more preferable in comparison to the iodometric method [1] as it provides the increased sensitivity, simplicity and rapid analysis, the absence of losses of released iodine due to its solid-phase extraction into the methacrylate polymer and can be conducted using the standard spectrophotometric equipment.
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固相分光光度法测定过氧化氢
提出了用甲基丙烯酸酯聚合物联合固相分光光度碘量测定过氧化氢的方法。该方法是基于碘离子与过氧化氢在盐酸中氧化反应,释放游离碘。用聚甲基丙烯酸酯基质提取碘,在365 nm吸光度下测定碘的浓度。聚甲基丙烯酸酯基质提取碘的量与溶液中过氧化氢的浓度成正比。研究了干扰离子的影响。最佳相接触时间为5分钟。研究了在分析溶液中加入盐酸对聚甲基丙烯酸酯基质与过氧化氢溶液接触后分析信号的影响。结果表明,在(3-5)∙10 -3 m的酸浓度范围内获得最大信号,分析溶液中碘化钾的最佳浓度为0.06%。在此浓度下,可检测浓度的范围最广,过氧化氢的检测限最小。所建立的方法保证了过氧化氢在(15-130)∙10 - 5%范围内的检测,检出限为5 × 10 - 5%。给出了该方法在消毒剂和漂白剂样品中过氧化氢含量的测定结果。与碘量法[1]相比,本文提出的过氧化氢测定方法更可取,因为它提供了更高的灵敏度,简单和快速的分析,并且由于其固相萃取到甲基丙烯酸酯聚合物中而没有释放碘的损失,并且可以使用标准分光光度法设备进行测定。
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来源期刊
Analitika i Kontrol
Analitika i Kontrol Chemistry-Analytical Chemistry
CiteScore
0.90
自引率
0.00%
发文量
15
期刊介绍: Analitika i Kontrol is a scientific journal covering theoretical and applied aspects of analytical chemistry and analytical control, published since autumn 1997. Founder and publisher of the journal is the Ural Federal University named after the first President of Russia Boris Yeltsin (UrFU, Ekaterinburg).
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