Extended Donnan model for ion partitioning in charged nanopores (2403.02796v1)

Abstract: Membranes consist of pores and the walls of these pores are often charged. In contact with an aqueous solution, the pores fill with water and ions migrate from solution into the pores until chemical equilibrium is reached. The distribution of ions between outside and pore solution is governed by a balance of chemical potential, and the resulting model is called a Donnan theory, or Donnan equation. Including a partitioning coefficient that does not depend on salt concentration results in an extended Donnan equation of the first kind'. Recently, an electrostatic model was proposed for ions in a pore based on the arrangement of ions around strands of polymer charge, including also ion activity coefficients in solution. That framework leads to an extended Donnan equationof the second kind', which has extra factors depending on ion concentrations in the pores and salt concentration in solution. In the present work, we set up another Donnan model of the second kind by evaluating the Coulombic interactions of ions in a cylindrical pore, including the interaction of ions with the charged pore walls and between the ions. We assume that counterions are near the pore wall while coions distribute over the center region. Starting from a complete analysis, we arrive at an elegant expression for the chemical potential of ions in such a pore. This expression depends on coion concentration, pore size, and other geometrical factors, but there is no additional dependence on counterion concentration and charge density. This model predicts the Coulombic contribution to the chemical potential in the pore to be small, much smaller than predicted by the electrostatic model from literature. Instead, we predict that up to around 1 M salt concentration, activity effects of ions in solution are more important.