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首页> 外文期刊>Analytical chemistry >Calibration-Free Ionophore-Based Ion-Selective Electrodes With a Co(II)/Co(III) Redox Couple-Based Solid Contact
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Calibration-Free Ionophore-Based Ion-Selective Electrodes With a Co(II)/Co(III) Redox Couple-Based Solid Contact

机译:基于Co(II)/ Co(III)氧化还原对的固体接触的免校准离子载体基离子选择电极

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摘要

A high electrode-to-electrode reproducibility of the emf response of solid contact ion-selective electrodes (SC-ISEs) requires a precise control of the phase boundary potential between the ion-selective membrane (ISM) and the underlying electron conductor. To achieve this, we introduced previously ionophore-free ion exchanger membranes doped with a well controlled ratio of oxidized and reduced species of a redox couple as redox buffer and used them to make SC-ISEs that exhibited highly reproducible electrode-to-electrode potentials. Unfortunately, ionophores were found to promote the loss of insufficiently lipophilic species from the ionophore-doped ISMs into aqueous samples. Here we report on an improved redox buffer platform based on equimolar amounts of the much less hydrophilic Co(III) and Co(II) complexes of 4,4'-dinonyl-2,2'-bipyridyl, which makes it possible to extend the redox buffer approach to ionophore-based ISEs. For example, K~+-selective electrodes based on the ionophore valinomycin exhibit electrode-to-electrode standard deviations as low as 0.7 mV after exposure of freshly prepared electrodes for 1 h to aqueous solutions. Exposure of freshly prepared ISE membranes to humidity prior to their first contact to electrolyte solution minimizes the initial (reproducible) emf drift. This redox buffer has also been successfully applied to sodium, potassium, calcium, hydrogen, and carbonate ion-selective electrodes, which all exhibit the high selectivity over interfering ions as expected for ionophore-doped ISE membranes.
机译:固体接触离子选择电极(SC-ISE)的电动势响应具有很高的电极间再现性,需要精确控制离子选择膜(ISM)和下面的电子导体之间的相界电势。为实现此目的,我们引入了以前无离子的离子交换膜,该膜中掺杂了氧化还原对的氧化和还原物种的比例得到很好控制的氧化还原对,并用它们来制造具有极高可再现电极间电势的SC-ISE。不幸的是,发现离子载体会促进不充分亲脂性的物种从掺杂离子载体的ISM丢失到水性样品中。在这里,我们报告了一种基于等摩尔量的4,4'-二壬基-2,2'-联吡啶基亲水性低得多的Co(III)和Co(II)配合物的改进的氧化还原缓冲剂平台,这使得可以扩展基于离子载体的ISE的氧化还原缓冲方法。例如,在将新鲜制备的电极暴露于水溶液1 h后,基于离子载体瓦里霉素的K + +选择性电极的电极间标准偏差低至0.7 mV。新制备的ISE膜在首次接触电解质溶液之前先暴露在湿气中,以最小化初始(可重现)电动势漂移。该氧化还原缓冲液也已成功应用于钠,钾,钙,氢和碳酸盐离子选择电极,这些电极对离子的掺杂具有很高的选择性,如离子载体掺杂的ISE膜所期望的。

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