Effect of solution ions on the charge and performance of nanofiltration membranes

被引:4
|
作者
Roth, Rebecca S. [1 ]
Birnhack, Liat [1 ]
Avidar, Mor [1 ]
Hjelvik, Elizabeth A. [2 ]
Straub, Anthony P. [2 ]
Epsztein, Razi [1 ]
机构
[1] Technion Israel Inst Technol, Fac Civil & Environm Engn, IL-32000 Hefa, Israel
[2] Univ Colorado, Dept Civil Environm & Architectural Engn, Boulder, CO 80309 USA
基金
美国国家科学基金会; 以色列科学基金会;
关键词
REVERSE-OSMOSIS; IONIZATION BEHAVIOR; ACTIVE LAYER; FUNCTIONAL-GROUPS; SURFACE-CHARGE; REJECTION; WATER; PH; TRANSPORT; SALT;
D O I
10.1038/s41545-024-00322-9
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Considering growing efforts to understand and improve the solute-specific selectivity of nanofiltration (NF) membranes, we explored the ion-specific effects that govern the charge and performance of a loose polyamide NF membrane that is commonly used for solute-solute separations. Specifically, we systematically evaluated the zeta potential of the membrane under different conditions of pH, salinity, and ionic composition, and correlated the obtained data with membrane performance tested under similar conditions. Our results identify the pK a of both carboxylic and amine groups bonded to the membrane surface and suggest that the highly polarizable chloride anions in the solution adsorb to the polyamide, increasing its negative charge. We also show that monovalent cations of different "stickiness" can neutralize the negative membrane charge to different extents due to their varying tendency to sorb to the polymer matrix or screen the fixed carboxyl groups on the membrane surface. Notably, our correlation between zeta potential measurements and permeability experiments indicates the substantial contribution of solution ions to Donnan exclusion in NF membranes.
引用
收藏
页数:9
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