Analyzing ion uptake in ion-exchange membranes using ion association model

被引:8
作者
Oren, Yaeli S. [1 ]
Nir, Oded [1 ]
Freger, Viatcheslav [2 ,3 ,4 ]
机构
[1] Ben Gurion Univ Negev, Zuckerberg Inst Water Res, Jacob Blaustein Inst Desert Res, Dept Desalinat & Water Treatment, Sede Boqer Campus, IL-8499000 Beer Sheva, Israel
[2] Technion IIT, Wolfson Dept Chem Engn, IL-32000 Haifa, Israel
[3] Technion IIT, Nancy & Stephen Grand Technion Energy Program, Haifa, Israel
[4] Technion IIT, Grand Water Res Inst, Haifa, Israel
基金
美国国家科学基金会; 欧盟地平线“2020”;
关键词
Membrane transport theory; Ion association and pairing; Ion exchange membranes; Ion partitioning; Ion permeability; Manning condensation; ACTIVITY-COEFFICIENTS; ELECTRODIALYSIS; CHLORIDE; NAFION;
D O I
10.1016/j.memsci.2023.122202
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Predicting ion uptake and selectivity in ion-exchange membranes is desired for many applications, yet a suitable physical description defining the most appropriate ion-specific parameters is still challenging. Here, we systematically develop an ion-association-based approach to modeling ion uptake in ion-exchange membranes from solutions of symmetric and non-symmetric salts. The model treats association in an ion-specific manner, selfconsistently accounting for equilibria between free ions in solution and within the membrane phase (salt injection) and between free and associated species within the membrane (association equilibria), subjects to overall membrane electroneutrality. The resulting models, including different possible association equilibria, were employed to fit the reported data for Nafion 117 and CR61 cation-exchange membranes in equilibrium with NaCl, MgCl2, CaCl2, and Na2SO4 single-salt solutions. The results are compared with the previously reported fits to the Manning condensation model, which shows that both models produce similarly good fits for NaCl, MgCl2, and CaCl2 solutions in the 0.01 to 1 M range. However, the greater flexibility and specificity of the association model allow addressing deviations observed for Na2SO4 solutions and for CaCl2 above 1 M as free-ion paring and possible formation of charged NaSO4- and CaCl+ pairs, respectively. The results demonstrate the present model may be a sound non-mean-field alternative to the Manning condensation model, capable of addressing ionspecificity and multiple modes of association.
引用
收藏
页数:8
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