Journal
ANALYTICAL CHEMISTRY
Volume 85, Issue 13, Pages 6208-6212Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ac400470n
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Funding
- Swiss National Science Foundation
- Australian Research Council [DP0987851]
- Australian Research Council [DP0987851] Funding Source: Australian Research Council
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Potentiometric sensors that exhibit a non-Hofineister selectivity sequence are normally designed by selective chemical recognition elements in the membrane. In other situations, when used as detectors in separation science, for example, membranes that respond equally to most ions are preferred. With so-called liquid membranes, a low selectivity is difficult to accomplish since these membranes are intrinsically responsive to lipophilic species. Instead, the high solubility of sample lipids in an ionophore-free sensing matrix results in a deterioration of the response. We explore here potentiometric sensors on the basis of ion-exchange membranes commonly used in fuel cell applications and electrodialysis, which have so far not found their way into the field of ion selective electrodes These membranes act as Donnan exclusion membranes as the ions are not stripped of their hydration shell as they interact with the membrane. Because of this, lipophilic ions are no longer preferred over hydrophilic ones, making them promising candidates for the detection of abundant ions in the presence of lipophilic ones or as detectors in separation science. Two types of cation exchanger membranes and one anion exchange membrane were characterized, and potentiometric measuring ranges were found to be Nernstian over a wide range down to about 10 mu M concentrations. Depending on the specific membrane, lipophllic ions gave equal response to hydrophilic ones or were even somewhat discriminated. The medium and long-term stability and reproducibility of the electrode signals were found to be promising when evaluated in synthetic and whole blood samples.
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