For charged porous membranes, the separation efficiency to charged particle
s and ions is affected by the electrical properties of the membrane surface
. Such properties are most commonly quantified in terms of zeta-potential.
In this paper, it is shown that the zeta-potential can be calculated numeri
cally from the membrane potential. The membrane potential expression for ch
arged capillary membranes in contact with electrolyte solutions at differen
t concentrations is established by applying the theory of non-equilibrium t
hermodynamic to the membrane process and considering the space-charge model
. This model uses the Nernst-Planck and Navier-Stokes equations for transpo
rt through pores, and the non-linear Poisson-Boltzmann equation, which is n
umerically solved, for the electrostatic condition of the fluid inside pore
s. The integral expressions of the phenomenological coefficients coupling t
he differential flow (solute relative to solvent) and the electrical curren
t with the osmotic pressure and the electrical potential gradients are esta
blished and calculated numerically. The mobilities of anions and cations ar
e individually specified. The variations of the membrane potential (or the
apparent transport number of ions in the membrane pores) are studied as a f
unction of different parameters: zeta-potential, pore radius, mean concentr
ation in the membrane, ratio of external concentrations and type of ions. (
C) 1999 Elsevier Science B.V. All rights reserved.