...
首页> 外文期刊>Analytical chemistry >Determination of Unbiased Selectivity Coefficients of Neutral Carrier-Based Cation-Selective Electrodes
【24h】

Determination of Unbiased Selectivity Coefficients of Neutral Carrier-Based Cation-Selective Electrodes

机译:中性载流子阳离子选择电极无偏选择性系数的确定

获取原文
获取原文并翻译 | 示例
           

摘要

A new procedure for the determination of selectivity coefficients of neutral carrier-based cation-selective electrodes is established that avoids exposure to the preferred ion prior to the measurement of discriminated ions. The method is, therefore, unbiased by the presence of preferred ions in the membrane that otherwise could mask the response to discriminated ion solutions. It is generally applicable as long as a series of considerations are met and can only be applied once for a given membrane. Careful studies with a series of sodium-, silver-, and calcium-selective electrodes reveal that Nernstian response slopes can now be obtained for even highly discriminated cations. Specifically, a 1,3-bridged calix[4]arene derivative as introduced by Yamamoto and Shinkai indeed yields an extraordinary sodium selectivity of log K↑(pot)↓(Na,k) = --4.9,with potassium showing Nernst response as well. Analogous measurements with two different silver carriers, a bisthioether-functionalized calix[4]arene and methylenebis(diisobutyldithiocarbamate), and the calcium carrier ETH 129 also show extremely high selectivity, which can satisfactorily be correlated to data obtained previously in ion-buffered solutions. The new procedure promises to be a valuable additional tool for future characterizations of highly selective ion carriers.
机译:建立了一种确定中性载体型阳离子选择性电极选择性系数的新程序,该程序可避免在测量被区分的离子之前暴露于优选离子中。因此,该方法不受膜中存在优选离子的偏见,否则这些离子会掩盖对已区分离子溶液的响应。只要满足一系列考虑,它通常是适用的,并且对于给定的膜只能应用一次。对一系列钠,银和钙选择性电极的仔细研究表明,即使对于高度区分的阳离子,现在也可以获得Nernstian响应斜率。具体而言,由Yamamoto和Shinkai引入的1,3-桥联杯[4]芳烃衍生物确实产生了非凡的钠选择性,log K↑(pot)↓(Na,k)= --4.9,钾的能斯特反应为好。用两种不同的银载体(双硫醚官能化的杯[4]亚芳基和亚甲基双(二异丁基二硫代氨基甲酸酯))和钙载体ETH 129进行的类似测量也显示出极高的选择性,这可以令人满意地与先前在离子缓冲溶液中获得的数据相关。新程序有望成为将来表征高选择性离子载体的有价值的附加工具。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号