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电位离子传感器的选择性

Selectivity of potentiometric ion sensors.

作者信息

Bakker E, Pretsch E, Bühlmann P

机构信息

Department of Chemistry, Aubum University, Alabama 36849, USA.

出版信息

Anal Chem. 2000 Mar 15;72(6):1127-33. doi: 10.1021/ac991146n.

Abstract

Selectivities of solvent polymeric membrane ion-selective electrodes (ISEs) are quantitatively related to equilibria at the interface between the sample and the electrode membrane. However, only correctly determined selectivity coefficients allow accurate predictions of ISE responses to real-world samples. Moreover, they are also required for the optimization of ionophore structures and membrane compositions. Best suited for such purposes are potentiometric selectivity coefficients as defined already in the 1960s. This paper briefly reviews the basic relationships and focuses on possible biases in the determination of selectivity coefficients. The traditional methods to determine selectivity coefficients (separate solution method, fixed interference method) are still the same as those originally proposed by IUPAC in 1976. However, several precautions are needed to obtain meaningful data. For example, errors arise when the response to a weakly interfering ion is also influenced by the primary ion leaching from the membrane. Wrong selectivity coefficients may be also obtained when the interfering agent is highly preferred and the electrode shows counterion interference. Recent advances show how such pitfalls can be avoided. A detailed recipe to determine correct potentiometric selectivity coefficients unaffected by such biases is presented.

摘要

溶剂聚合膜离子选择性电极(ISEs)的选择性与样品和电极膜之间界面处的平衡存在定量关系。然而,只有正确测定的选择性系数才能准确预测ISEs对实际样品的响应。此外,它们也是优化离子载体结构和膜组成所必需的。最适合此类目的的是早在20世纪60年代就已定义的电位选择性系数。本文简要回顾了基本关系,并重点关注选择性系数测定中可能存在的偏差。测定选择性系数的传统方法(分别溶液法、固定干扰法)仍与1976年国际纯粹与应用化学联合会(IUPAC)最初提出的方法相同。然而,为了获得有意义的数据,需要采取一些预防措施。例如,当对弱干扰离子的响应也受到膜中主离子浸出的影响时,就会产生误差。当干扰剂被高度优先选择且电极表现出抗衡离子干扰时,也可能获得错误的选择性系数。最新进展展示了如何避免这些陷阱。本文给出了一个详细的方法来测定不受此类偏差影响的正确电位选择性系数。

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