Water and ion sorption in a series of cross-linked AMPS/PEGDA hydrogel membranes
Charge density of ion exchange membranes (IEMs) profoundly influences water and ion sorption. However, fundamental studies of water and ion sorption in charged membranes over a wide range of charge densities are not widely available, which makes it difficult to establish fundamental structure/proper...
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Veröffentlicht in: | Polymer (Guilford) 2018-06, Vol.146, p.196-208 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Charge density of ion exchange membranes (IEMs) profoundly influences water and ion sorption. However, fundamental studies of water and ion sorption in charged membranes over a wide range of charge densities are not widely available, which makes it difficult to establish fundamental structure/property relations in such materials. In this study, a series of homogeneous cross-linked uncharged and sulfonated hydrogel membranes were prepared using poly(ethylene glycol diacrylate) (PEGDA) copolymerized with 2-acrylamido-2-methylpropanesulfonic acid (AMPS). Equilibrium water uptake and ion content (Na+, Cl−) in the membranes were determined as a function of external NaCl concentration (0.01–1.0 mol/L). As polymer fixed charge density increased, both water and counter-ion (Na+) sorption increased. Co-ion (Cl−) sorption decreased markedly with only modest increases in polymer fixed charge density, suggesting that even low levels of fixed charges exclude co-ions significantly. However, Cl− sorption became independent of charge density at higher levels of charge density. Experimental values for sorbed Cl− concentrations deviated from those obtained via ideal Donnan model due to thermodynamic non-idealities of ions in the solution and membrane phases.
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•Low levels of added fixed charges exclude co-ions significantly.•Ideal Donnan model cannot quantitatively describe experimental data due to non-idealities of ion activity coefficients.•Membrane ion activity coefficients are correlated with water uptake and fixed charge concentration. |
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ISSN: | 0032-3861 1873-2291 |
DOI: | 10.1016/j.polymer.2018.05.021 |