Cation-exchange membranes allow preferential passage of cations over anions, but they show minimal selectivity among cations, which limits their use in ion separations. Recent studies show that modification of cation-exchange membranes with polyelectrolyte multilayers leads to exceptional monovalent/divalent cation electrodialysis selectivities, but no studies report high selectivity among monovalent ions. This work demonstrates that adsorption of protonated poly(allylamine) (PAH)/poly(4-styrenesulfonate) (PSS) multilayers on Nafion membranes leads to high K+/Li+ selectivities in Donnan dialysis, where K+ and Li+ ions in a source phase pass through the membrane and exchange with Na+ ions in a receiving phase. Addition of 0.01 M HNO3 to a source phase containing 0.01 M KNO3 and 0.01 M LiNO3 increases the KE/Li+ selectivity from 8 to similar to 60 through (PAH/PSS)(5)PAH-coated Nafion membranes, primarily because of a >= fivefold increase in K+ flux. These selectivities are much larger than the ratio of 1.9 for the aqueous diffusion coefficients of K and Li+, and uncoated Nafion membranes give a K+/Li+ selectivity <3. Bi-ionic transmembrane potential measurements at neutral pH confirm that the membrane is more permeable to 1(4 than Li+, but this selectivity is less than in Donnan dialysis with acidic solutions. In situ ellipsometry data indicate that PAH/PSS multilayers (assembled at pH 2.3, 7.5, or 9.3) swell at pH 2.0, and this swelling may open cation exchange sites that preferentially bind K+ to enable highly selective transport. The coated membranes also exhibit modest selectivity for K+ over H+, suggesting selective transport based on preferential partitioning of K+ into the coatings. Selectivity declines when increasing the source-phase KNO3 concentration to 0.1 M, perhaps because the discriminating transport pathway saturates. Moreover, selectivities are lower in electrodialysis than in Donnan dialysis, presumably because electrodialysis engages other transport mechanisms, such as electroosmosis and strong electromigration.
机构:
Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USAUniv Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
Ahmad, Muhammad
Yaroshchuk, Andriy
论文数: 0引用数: 0
h-index: 0
机构:
ICREA, Pg L Co 23, Barcelona 08010, Spain
Univ Politecn Cataluna, Dept Chem Engn, Av Diagonal 647, Barcelona 08028, SpainUniv Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
Yaroshchuk, Andriy
Bruening, Merlin L.
论文数: 0引用数: 0
h-index: 0
机构:
Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USAUniv Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA