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过氧乙酸和过氧化氢的同步电分析

Simultaneous electroanalysis of peroxyacetic acid and hydrogen peroxide.

作者信息

Awad M I, Harnoode C, Tokuda K, Ohsaka T

机构信息

Department of Electronic Chemistry, Interdisciplinary Graduate School of Science and Engineering, Tokyo Institute of Technology, 4259 Nagatsuta, Midori-ku, Yokohama 226-8502, Japan.

出版信息

Anal Chem. 2001 Apr 15;73(8):1839-43. doi: 10.1021/ac001217e.

Abstract

The electrochemical behavior of peroxyacetic acid (PAA) in the presence of hydrogen peroxide (H2O2) has been investigated using cyclic voltammetry and hydrodynamic techniques [rotating disk electrode (RDE) voltammetry and rotating ring-disk electrode (RRDE) voltammetry]. The results have been analyzed aiming at simultaneous electroanalysis of both species. Glassy carbon and gold electrodes were used for this investigation. It was found that the reduction of PAA, as well as H2O2, is highly sensitive to the electrode material; for example, at 100 mV s-1, the reduction peak potentials of PAA were 0.2 and -1.1 V at gold and glassy carbon electrodes, respectively. The well-separated steady-state limiting currents were obtained using a gold electrode for the reduction of both PAA and H2O2 and also a well-defined one for the oxidation of H2O2. On the basis of the RDE experiments, good calibration curves were obtained for both species over a wide range of their concentrations, for PAA and H2O2 in the range of 0.36 to 110 and 0.11 to 34 mM, respectively. The simultaneous and selective electroanalysis of PAA and H2O2 in their coexistence is demonstrated for the first time.

摘要

采用循环伏安法和流体动力学技术(旋转圆盘电极(RDE)伏安法和旋转环盘电极(RRDE)伏安法)研究了过氧化氢(H₂O₂)存在下过氧乙酸(PAA)的电化学行为。针对两种物质的同时电分析对结果进行了分析。本研究使用了玻碳电极和金电极。结果发现,PAA以及H₂O₂的还原对电极材料高度敏感;例如,在100 mV s⁻¹时,PAA在金电极和玻碳电极上的还原峰电位分别为0.2 V和 -1.1 V。使用金电极对PAA和H₂O₂进行还原以及对H₂O₂进行氧化时,均获得了分离良好的稳态极限电流。基于RDE实验,两种物质在其浓度的较宽范围内均获得了良好的校准曲线,PAA和H₂O₂的浓度范围分别为0.36至110 mM和0.11至34 mM。首次证明了在PAA和H₂O₂共存时对它们进行同时和选择性电分析的可行性。

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