Specific ion effects on the permselectivity of sulfonated poly (ether sulfone) cation exchange membranes

被引:113
作者
Cassady, Harrison J. [1 ]
Cimino, Emily C. [2 ]
Kumar, Manish [1 ]
Hickner, Michael A. [2 ]
机构
[1] Penn State Univ, Dept Chem Engn, University Pk, PA 16802 USA
[2] Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16802 USA
关键词
Ion-exchange membrane; Permselectivity; Membrane potential; Counter-ion; Co-ion; Reverse electrodialysis; AEM; CEM; REVERSE ELECTRODIALYSIS; POWER-GENERATION; TECHNOLOGIES; SOLVATION; WATER;
D O I
10.1016/j.memsci.2016.02.048
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Water uptake and permselectivity were measured for five sulfonated poly(ether sulfone) cation exchange membranes with varying degrees of functionalization from 20% to 60%. Experiments were conducted in aqueous salt solutions of LiCl, NaCl, KCl, Li2SO4, Na2SO4 and K2SO4 to isolate the effect of counter-ions and co-ions on membrane permselectivity. Water uptake ranged from 0.13 g(water)/g(polymer) to 0.76 g(water)/g(polymer) depending on the degree of functionalization and salt used, but was not found to describe the perms electivity differences between salts as the counter-ion and co-ion were varied. This lack of correlation between water uptake and permselectivity is counter to expectations for swollen polymers. Counter-ion binding affinity, charge density and dilute solution mobility were identified as factors influencing membrane permselectivity. Specifically, counter-ions with higher binding affinities to the fixed charge group of the polymer showed lower permselectivities due to counter-ion condensation. Co-ion polarizability was identified as the primary factor for co-ion effects on permselectivity, with more polarizable co-ions resulting in lower membrane permselectivities. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:146 / 152
页数:7
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