Grygolowicz-Pawlak Ewa, Bakker Eric
Nanochemistry Research Institute, Department of Chemistry, Curtin University of Technology, Perth, WA 6845, Australia.
Electrochem commun. 2010 Sep 1;12(9):1195-1198. doi: 10.1016/j.elecom.2010.06.017.
A promising method for the elimination of undesired capacitive currents in view of realizing a potentially calibration free coulometric ion detection system is presented. The coulometric cell is composed of a porous polypropylene tube doped with a liquid calcium-selective membrane and a silver/silver chloride wire as an inner electrode, forming a thin layer sample between wire and tubing. The total charge passed through the system during potential controlled electrolysis of the thin layer sample is indeed found to be proportional to the amount of calcium present, but non-Faradaic processes do contribute to the obtained signal. We introduce here a multi-pulse procedure that allows one to perform a second excitation pulse at the same excitation potential after exhaustive ion transfer voltammetry of calcium has taken place. The intercept of the calibration curve after background subtraction is found as 20.6 +/- 0.6 muC, significantly lower than the value of 54.1 +/- 0.8 muC for the uncorrected curve. Changes in sample temperature (from 23 degrees C to 38 degrees C) did equally not affect the background corrected coulometric readings, supporting that the procedure renders the readout principle more robust.
为了实现一个潜在的免校准库仑离子检测系统,本文提出了一种消除不需要的电容电流的有效方法。库仑池由一根掺杂有液体钙选择性膜的多孔聚丙烯管和一根银/氯化银线作为内电极组成,在电极线和管之间形成一个薄层样品。在对薄层样品进行恒电位电解过程中,通过系统的总电荷量确实与存在的钙含量成正比,但非法拉第过程确实对获得的信号有贡献。我们在此引入一种多脉冲程序,该程序允许在钙的彻底离子转移伏安法之后,在相同的激发电位下执行第二个激发脉冲。背景扣除后校准曲线的截距为20.6±0.6 μC,明显低于未校正曲线的54.1±0.8 μC的值。样品温度(从23℃到38℃)的变化同样不影响背景校正后的库仑读数,这支持了该程序使读出原理更稳健。