Deviations from Electroneutrality in Membrane Barrier Layers: A Possible Mechanism Underlying High Salt Rejections
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- 作者：Andriy Yaroshchuk ; Yan Zhu ; Mykola Bondarenko ; Merlin L. Bruening
- 刊名：Langmuir
- 出版年：2016
- 出版时间：March 22, 2016
- 年：2016
- 卷：32
- 期：11
- 页码：2644-2658
- 全文大小：647K
- ISSN：1520-5827
文摘
Reverse osmosis and nanofiltration (NF) employ composite membranes whose ultrathin barrier layers are significantly more permeable to water than to salts. Although solution-diffusion models of salt transport through barrier layers typically assume ubiquitous electroneutrality, in the case of ultrathin selective skins and low ion partition coefficients, space-charge regions may occupy a significant fraction of the membrane barrier layer. This work investigates the implications of these deviations from electroneutrality on salt transport. Both immobile external surface charge and unequal cation and anion solvation energies in the barrier layer lead to regions with excess mobile charge, and the size of these regions increases with decreasing values of either feed concentrations or ion partition coefficients. Moreover, the low concentration of the more excluded ion in the space-charge region can greatly increase resistance to salt transport to enhance salt rejection during NF. These effects are especially pronounced for membranes with a fixed external surface charge density whose sign is the same as that of the more excluded ion in a salt. Because of the space-charge regions, the barrier-layer resistance to salt transport initially rises rapidly with increasing barrier thickness and then plateaus or even declines within a certain thickness range. This trend in resistance implies that thin, defect-free barrier layers will exhibit higher salt rejections than thicker layers during NF at a fixed transmembrane pressure. Deviations from electroneutrality are consistent with both changes in NF salt rejections that occur upon changing the sign of the membrane fixed external surface charge, and CaCl2 rejections that in some cases may first decrease, then increase and then decrease again with increasing CaCl2 concentrations in NF feed solutions.