Department of Chemistry, University of Warsaw, Pasteura 1, 02-093 Warsaw, Poland.
Talanta. 2011 May 15;84(3):814-9. doi: 10.1016/j.talanta.2011.02.018. Epub 2011 Feb 19.
A new method of quantitative incorporation of primary cations into ion-selective membrane by means of galvanostatic cathodic polarization/conditioning, before measurement step, was proposed and tested on the example of potassium-selective electrode with ionophore - valinomycin in poly(vinyl chloride) based membrane and with polypyrrole solid contact. Open circuit potential values recorded after polarization can be quantitatively explained by changes of primary cations and ionophore concentration in the surface part of the membrane. The influence of potassium ions concentration in the membrane (in relation to ion exchange sites amount) on the shape of potentiometric calibration plots was also observed. Improved characteristics, with extended linear range, can be obtained for membrane of minor loading with primary cations (around 25%), the responses are relatively stable in course of following calibrations.
提出了一种通过恒电流阴极极化/调理在测量步骤之前将初级阳离子定量掺入离子选择性膜中的新方法,并以聚(氯乙烯)基膜中含有缬氨霉素的钾选择性电极和聚吡咯固体接触为例进行了测试。极化后记录的开路电位值可以通过膜表面部分的初级阳离子和载体浓度的变化来定量解释。还观察到膜中钾离子浓度(与离子交换位数量有关)对电位校准曲线形状的影响。对于初级阳离子负载量较小的膜(约 25%),可以获得改进的特性,线性范围得到扩展,响应在后续校准过程中相对稳定。