Fundamentals of Selective Ion Transport Through Multilayer Polyelectrolyte Films

Monday, June 11, 2012
La Salle A/B (InterContinental New Orleans)
Chao Cheng1, Andriy Yaroshchuk2 and Merlin L. Bruening1, (1)Chemistry Department, Michigan State University, East Lansing, MI, (2)ICREA and Department of Chemical Engineering, Polytechnic University of Catalonia, Barcelona, Spain

Membranes composed of multilayer poly(sodium 4-styrenesulfonate) (PSS)/protonated poly(allylamine) (PAH) films on porous supports exhibit high monvovalent/divalent ion selectivities, particularly for cations. Remarkably, the diffusion dialysis K+/Mg2+ selectivity is >1000. However, the nanofiltration K+/Mg2+ selectivity is only 15 with these membranes, suggesting some convective coupling in ion transport. Membrane potentials with MgCl2 solutions at different concentrations at the feed and permeate sides of the membrane show Cl- transport numbers approaching 1. In nanofiltration, the high asymmetry of membrane permeabilities with respect to cations and anions (reflected by the high Cl- transport number) creates high filtration potentials that give rise to large negative rejections of trace monovalent cations such as K+, Li+ and Cs+. When MgCl2 is the dominant feed salt, concentrations of K+ and Cs+ in the permeate can reach nearly 3 times those in the feed. Under the experimental conditions, negative rejections increase in magnitude with both decreasing flow rate and increasing mobility of trace monovalent cation. Knowledge of single-ion permeabilities is vital for predicting the performance of these membranes in diffusion dialysis or nanofiltration with mixed salt solutions.

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