Elucidation of Ion-Pairing Elution Behavior of Anions and Cations in Electrostatic Ion Chromatography Using Water as a Mobile Phase

T. Umemura
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引用次数: 1

Abstract

Peculiar ion-pairing elution behavior of analyte anions with counter cations in electrostatic ion chromatography (EIC) using water as a mobile phase was theoretically elucidated based on the Donnan membrane equilibrium principle and charge balance condition. New parameters, f anion and f cation , containing a fluctuating coefficient, x , which corresponded to capacity factors, were derived from the Donnan equation. The f anion and f cation of the constituent anion and cation in ion-pairing elution were connected with each other by the x , and the capacity factor, k ion pair (of co-eluting anion and cation) could be predicted by solving the relation of f anion = f cation for x . The elution volumes for various ion pairs thus semiempirically calculated were in good agreement with those experimentally obtained. In addition, the selective ion-pairing formation in EIC could reasonably be explained by applying the parameters to a modified classical plate theory.
以水为流动相的静电离子色谱法中阴离子和阳离子离子配对洗脱行为的阐明
基于Donnan膜平衡原理和电荷平衡条件,从理论上阐明了以水为流动相的静电离子色谱(EIC)中分析物阴离子与抗衡阳离子的独特离子配对洗脱行为。从Donnan方程导出了新的参数f阴离子和f阳离子,其中包含与容量因子相对应的波动系数x。离子对洗脱中组成阴离子和阳离子的f阴离子和f阳离子通过x相互连接,通过求解x的f阴离子=f阳离子的关系,可以预测(共洗脱阴离子和阳离子)容量因子k离子对。由此半经验计算的各种离子对的洗脱体积与实验获得的洗脱体积非常一致。此外,通过将这些参数应用于修正的经典板理论,可以合理地解释EIC中选择性离子配对的形成。
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