Overlimiting current by interactive ionic transport between space charge region and electric double layer near ion-exchange membranes

Desalination ◽  
2012 ◽  
Vol 285 ◽  
pp. 245-252 ◽  
Author(s):  
Younggy Kim ◽  
Desmond F. Lawler
2007 ◽  
Vol 579 ◽  
pp. 173-226 ◽  
Author(s):  
B. ZALTZMAN ◽  
I. RUBINSTEIN

Electric conduction from an electrolyte solution into a charge selective solid, such as ion exchange membrane or electrode, becomes unstable when the electrolyte concentration near the interface approaches zero owing to diffusion limitation. The sequence of events leading to instability is as follows: upon the decrease of the interface concentration, the electric double layer at the interface transforms from its common quasi-equilibrium structure to a different, non-equilibrium one. The key feature of this new structure is an extended space charge added to the usual one of the quasi-equilibrium electric double layer. The non-equilibrium electro-osmotic slip related to this extended space charge renders the quiescent conductance unstable. A unified asymptotic picture of the electric double-layer undercurrent, encompassing all regimes from quasi-equilibrium to the extreme non-equilibrium one, is developed and employed for derivation of a universal electro-osmotic slip formula. This formula is used for a linear stability study of quiescent electric conduction, yielding the precise parameter range of instability, compared with that in the full electroconvective formulation. The physical mechanism of instability is traced both kinematically, in terms of non-equilibrium electro-osmotic slip, and dynamically, in terms of forces acting in the electric double layer.


2021 ◽  
Vol 51 (1) ◽  
pp. 21-46
Author(s):  
Klaus-Dieter Kreuer ◽  
Andreas Münchinger

This review discusses selective and fast transport of ionic species (ions and their associates) through systems as diverse as ion-conducting transmembrane proteins and ion exchange membranes (IEMs) in aqueous environments, with special emphasis on the role of electrostatics, specific chemical interactions, and morphology (steric effects). Contrary to the current doctrine, we suggest that properly balanced ion-coordinating interactions are more important than steric effects for selective ion transport in biological systems. Steric effects are more relevant to the selectivity of ionic transport through IEMs. As a general rule, decreased hydration leads to higher selectivity but also to lower transport rate. Near-perfect selectivity is achieved by ion-conducting channels in which unhydrated ions transfer through extremely short hydrophobic passages separating aqueous environments. In IEMs, ionic species practically keep their hydration shell and their transport is sterically constrained by the width of aqueous pathways. We discuss the trade-off between selectivity and transport rates and make suggestions for choosing, optimizing, or developing membranes for technological applications such as vanadium-redox-flow batteries.


1993 ◽  
Vol 97 (32) ◽  
pp. 8524-8530 ◽  
Author(s):  
J. A. Manzanares ◽  
W. D. Murphy ◽  
S. Mafe ◽  
H. Reiss

AIChE Journal ◽  
1990 ◽  
Vol 36 (7) ◽  
pp. 1061-1074 ◽  
Author(s):  
Angel G. Guzmán-Garcia ◽  
Peter N. Pintauro ◽  
Mark W. Verbrugge ◽  
Robert F. Hill

Sign in / Sign up

Export Citation Format

Share Document