Mixed potential, ITIES

Of fundamental importance in understanding the electrochemistry of ion-selective membranes and also of biomembranes is the research in the field of voltammetry at ITIES mainly pioneered by Koryta and coworkers 99 101 . Koryta also demonstrated convincingly that a treatment like corroding metal electrodes is possible 102). For the latter, the description in the form of an Evans-diagram is most appropriate Fig. 4 shows schematically some mixed potentials, which are likely to arise at cation-selective membranes if interfering ions disturb an ideal Nernstian behavior82. Here, the vertical axis describes the galvani potential differences (absolute po-... 

The potential built at the interface in the presence of the transfer of more than one ionic species is a kind of mixed potential, as pointed out by Koryta in the context of ion-selective electrodes [45]. The theory of the mixed potential at the ITIES was presented for the case in the presence of supporting electrolyte [46] and then extended to the case in the absence of supporting electrolyte [47]. Consider the cell... 

If T terface and Tbuik replace Ca, equilibrium and Ca, bulks respectively, in the definition of the dimensionless profile P, and the thermal diffusiv-ity replaces a. mix. then the preceding equation represents the thermal energy balance from which temperature profiles can be obtained. The tangential velocity component within the mass transfer boundary layer is calculated from the potential flow solution for vg if the interface is characterized by zero shear and the Reynolds number is in the laminar flow regime. Since the concentration and thermal boundary layers are thin for large values of the Schmidt and Prandtl... 

The formulas 3 7 describe all the production possibilities new components, mix of new-old, old components used in a new product. If a producer has sufTicient data required to estimate the rehabil-ity functions of product elements, the calculations of potential profit from the reusing pohcy should not be very difficult for a given cost components and the length of a warranty period. 

The interaction of hydrocarbon and fluorocarbon surfactants on the surface of dispersed particles has been studied through a flocculation and redispersion process [65-67]. Dispersions of positively charged particles can be flocculated with an anionic surfactant. An excess of the anionic surfactant forms a bilayer on the particle surface and causes redispersion of the flocculated sol. This flocculation reversal was used to study the interaction between mixed surfactants on a solid surface. A dispersion of iron(ITI) oxide hydrate particles was flocculated with an anionic hydrocarbon or fluorocarbon surfactant at pH 3.5, where the sols had a positive zeta potential. Subsequently, a second fluorocarbon or hydrocarbon surfactant was added to the flocculated sol. The extent of redispersion depended on the interaction between the two surfactants on the solid particle surface. 

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