Some insights into the facilitated ion transfer voltammetric responses at ITIES exhibiting interfacial and bulk membrane kinetic effects.

General analytical equations corresponding to the Facilitated Ion Transfer (FIT) at ITIES (Interface between Two Immiscible Electrolyte Solutions) are presented for the most frequent case in which the complexing agent is present only in the organic phase, and considering both the ion transfer and the chemical complexation kinetic effects. Under these conditions, the FIT process can be regarded as an EC mechanism. This study is of great interest to elucidate the origin of the kinetic effects which affect the electrochemical signal.

Normal perfusion pressure breakthrough phenomenon: what still remains unknown.

We report two cases of normal perfusion pressure breakthrough phenomenon after total brain arteriovenous malformation removal. Hereby, we demonstrate that not only autoregulation impairment in the ipsilateral hemisphere occurs but also contralateral remote vessels response does. Such findings may be observed at 2-4 weeks and may resolve after 1-3 months.

Kinetic effects of the complexation reaction in the facilitated ion transfer at liquid membrane systems of one and two polarized interfaces. Theoretical insights.

An in-depth study of the ion transfer facilitated by complexation in the organic phase (TOC mechanism) in liquid membrane systems of one and two polarized interfaces is carried out by taking into account the kinetic effects associated with the complexation reaction. Explicit analytical equations for the normal pulse voltammetric (I/E) and chronoamperometric (I/t) responses with an explicit dependence on the kinetic parameters of the chemical complexation are presented for both kinds of membrane system, which could be useful for modeling artificial and biological membranes. The equations are compared with those obtained by using the widely used approximation of total equilibrium conditions that leads to the transfer by interfacial complexation mechanism (TIC), which only depends on thermodynamic parameters.

Physical insights of salt transfer through solvent polymeric membranes by means of electrochemical methods.

A combined voltammetric study of the joint transfer of the two constituting ions of a water-soluble salt has been carried out using normal-pulse voltammetry, linear-sweep voltammetry and square-wave voltammetry in a system with two liquid-liquid polarized interfaces. As a result, we have explained the voltammetric features that allow us to distinguish this uptake from that corresponding to two equally charged ions, in spite of the appearance in both situations of two current peaks with the same sign in both square-wave and linear-sweep voltammograms, and we have found that linear-sweep voltammetry and square-wave voltammetry complement each other excellently.A theoretical comparison with a system of a single polarized interface has also been made, showing that these systems are much less appropriate for characterizing these salt-ion transfers.

Square wave voltcoulometry: a tool for the study of strongly adsorbed redox molecules.

A new multipotential pulse technique called square wave voltcoulometry (SWVC), based on the analysis of the difference of converted charge signals obtained between two successive half-cycles when a square wave potential is applied, is developed to study charge-transfer processes taking place in electroactive monolayers. The use of SWVC presents the advantage of giving rise to a peak-shaped response, which evolves to a charge plateau at high square wave pulse amplitudes, from which the total surface excess and the formal potential can be immediately measured for quasi-reversible and reversible processes. This characteristic represents its main advantage versus other multipotential step techniques, which lead to a negligible current under reversible conditions.