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Zeroth-order solution and higher-order corrections for the CE mechanism in double potential step techniques

机译:双电位阶跃技术中CE机制的零阶解和高阶校正

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摘要

The general solution for all modes of double-pulse voltammetry for an electrode process under Nernstian behaviour coupled with a prior fast first order chemical reaction (CE mechanism) has been derived. This allows us to describe the characteristics of differential pulse polarography (DPP), differential normal pulse polarography (DNPP), reverse pulse polarography (RPP), and double potential step chronoamperometric responses, among others. Also, quantitative kinetic data analysis that allows us to determine the rate constants of the chemical reaction from these responses is discussed. It is worth emphasizing that the DNPP and chronoamperometric responses can be examined since the solution obtained is not limited by the restriction t'/t 1 (where t' is the duration of the second step), and this is due to the fact that the current response as t' increases can be computed to any degree of accuracy by including as many higher-order corrections as necessary. A comparative study with the predictions of the solution previously reported by Kim and Birke (Anal. Chem., 55 (1983) 1735) for the DPP response involved with this mechanism is presented.
机译:推导了在能斯特行为下电极过程中所有模式双脉冲伏安法的一般解决方案,以及先前的快速一阶化学反应(CE机理)。这使我们能够描述差分脉冲极谱法(DPP),差分正常脉冲极谱法(DNPP),反向脉冲极谱法(RPP)和双电位阶跃计时电流法响应等特性。此外,还讨论了定量动力学数据分析,该分析使我们能够从这些响应确定化学反应的速率常数。值得强调的是,可以检查DNPP和计时电流响应,因为获得的解不受t'/ t 1的限制(其中t'是第二步的持续时间),这是由于事实通过增加所需的尽可能多的高阶校正,可以将t'增大时的电流响应计算到任何精度。提出了一项比较研究,该研究对Kim和Birke先前报道的解决方案的预测(Anal。Chem。,55(1983)1735)对涉及该机制的DPP反应进行了介绍。

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