RESUMO
Passing currents through ion-selective membranes has contributed to the development of a variety of novel methods. In this work, chronopotentiometric (CP) transients with two transition times (breakpoints) are presented for the first time, with the theoretical interpretation of such voltage transients. The validity of our theory has been confirmed in experiments utilizing ETH 5294 chromoionophore-based pH sensitive membranes with and without lipophilic background electrolyte and ETH 5234 ionophore-based calcium selective membranes in which the ionophore forms 3:1 complexes with Ca(2+) ions. The conditions under which two breakpoints can be identified in the chronopotentiometric voltage transients are discussed.Spectroelectrochemical microscopy (SpECM) is used to show that the two breakpoints in the CP curves emerge approximately when the free ionophore and ion-ionophore complex concentrations approach zero at the opposite membrane-solution interfaces. The two breakpoint times can be utilized to follow simultaneously the concentration changes of the free ionophore, the ion-ionophore complex, and the mobile anionic sites in cation-selective membranes. In membranes with known composition, the time instances where breakpoints occur can be used to estimate the free ionophore and the ion-ionophore complex diffusion coefficients.
RESUMO
The diffusion coefficients of active components in ion-selective membranes have a decisive influence on the life-time and detection limit of the respective ion-selective electrodes, as well as influencing the rate of polarization and relaxation processes of electrically perturbed ion sensors. Therefore, the rational design of mass transport controlled ion-selective electrodes with sub-nanomolar detection limits requires reliable data on the diffusion coefficients. We have implemented electrochemical methods for the quantitative assessment of both the diffusion coefficients of free ionophores and ion-ionophore complexes. The diffusion coefficients of the pH-sensitive chromoionophore ETH 5294 and the calcium-selective ionophore ETH 5234 were determined in plasticized PVC membranes with different PVC to plasticizer ratios. The diffusion coefficient of the free chromoionophore determined by a chronoamperometric method was validated with optical methods for a variety of membrane compositions. The calcium-selective ionophore ETH 5234 was used as a model compound to assess the diffusion coefficient of the ion-ionophore complex calculated from the time required for the complexes to cross a freshly prepared membrane during potentiometric ion-breakthrough experiments. The difference between the diffusion coefficients of the free ionophore ETH 5234 and the ion-ionophore complex was found to be significant and correlated well with the geometry of the respective species.
