Transport in polymer membranes beyond linear response: Controlling permselectivity by the driving force

Abstract

In the popular solution-diffusion picture, the membrane permeability is defined as the product of the partition ratio and the diffusivity of penetrating solutes inside the membrane in the linear response regime, i.e., in equilibrium. However, of practical importance is the penetrants' flux across the membrane driven by external forces. Here, we study nonequilibrium membrane permeation orchestrated by a uniform external driving field using molecular computer simulations and continuum (Smoluchowski) theory in the stationary state. In the simulations, we explicitly resolve the penetrants' transport across a finite monomer-resolved polymer network, addressing one-component penetrant systems and mixtures. We introduce and discuss possible definitions of nonequilibrium, force-dependent permeability, representing `system' and `membrane' permeability. In particular, we present for the first time a definition of the differential permeability response to the force. We demonstrate that the latter turns out to be significantly nonlinear for low-permeable systems, leading to a high amount of selectiveness in permeability, called `permselectivity', and is tunable by the driving force. Our continuum-level analytical solutions exhibit remarkable qualitative agreement with the penetrant- and polymer-resolved simulations, thereby allowing us to characterize the underlying mechanism of permeabilities and steady-state transport beyond the linear response level.

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Cited by in corpus (3)

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• Feedback-controlled solute transport through chemo-responsive polymer membranes
• Nonequilibrium friction and free energy estimates for kinetic coarse-graining -- Driven particles in responsive media