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Electrochemical evaluation of the a carbon-paste electrode modified with spinel manganese(IV) oxide under flow conditions for amperometric determination of lithium

机译:尖晶石型锰(IV)氧化物修饰的碳糊电极在流动条件下的电化学评估,用于电流法测定锂

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摘要

The participation of cations in redox reactions of manganese oxides provides an opportunity for development of chemical sensors for non-electroactive ions. This paper describes the amperometric determination of lithium ions using carbon-paste electrode modified with spinel manganese(IV) oxide under flow conditions. Systematic investigations were made to optimize the experimental parameters for lithium sensor by flow injection analysis. The detection was based on the measurement of anodic current generated by oxidation of Mn(III) to Mn(IV) at the surface of the electrode and consequently the lithium ions extraction into the spinel structure. An operating potential of 0.50 V (vs. Ag/AgCl/3 KCl mol/L) was exploited for amperometric monitoring. The amperometric signal was linearly dependent on the lithium ions concentration over the range 4.0 x 10(-5) to 1.0 x 10(-3) mol L-1. The equilibrium constant of insertion/extraction of the lithium ion in the spine! structure, apparent Gibbs energy of insertion, and surface coverage of the electrode with manganese oxide, were calculated by peak charge (Q) in different concentration under flow conditions. Considering selectivity, the peak charge of the sensor was found to be linearly dependent on the ionic radius of the alkaline and earth-alkaline cations. (C) 2010 Elsevier Ltd. All rights reserved.
机译:阳离子参与锰氧化物的氧化还原反应为开发用于非电活性离子的化学传感器提供了机会。本文介绍了在流动条件下使用尖晶石型锰(IV)氧化物修饰的碳糊电极对锂离子进行安培测定的方法。通过流动注射分析进行系统研究以优化锂传感器的实验参数。该检测基于对通过在电极表面将Mn(III)氧化为Mn(IV)并由此将锂离子提取到尖晶石结构中而产生的阳极电流的测量。利用0.50 V(vs. Ag / AgCl / 3 KCl mol / L)的工作电势进行安培监测。安培信号线性依赖于锂离子浓度范围为4.0 x 10(-5)至1.0 x 10(-3)mol L-1。锂离子在脊柱中的插入/拔出平衡常数!通过在流动条件下不同浓度下的峰值电荷(Q)计算结构,表观Gibbs插入能以及电极的氧化锰表面覆盖率。考虑到选择性,发现传感器的峰值电荷与碱金属和碱土金属阳离子的离子半径线性相关。 (C)2010 Elsevier Ltd.保留所有权利。

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