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Updated: Jan 11, 2026

Ion-Exchange Membranes for the Fabrication of Reverse Electrodialysis Device
Published on: July 20, 2021
Architected Composite Reverse Osmosis Membrane with Multibarrier for Enhanced Ammonium Selectivity
Yi-Yu Ling1, Ke-Xin Yuan1, Siming Xie1
1State Key Laboratory of Urban Water Resources and Environment, Harbin Institute of Technology, Harbin 150090, PR China.
Abstract:
To overcome the limited ammonium (NH4+-N) rejection (∼93%) of conventional reverse osmosis (RO) membranes in wastewater treatment, a novel thin-film composite RO (TFC-RO) membrane with ammonium-rejecting functional "fillings" throughout the polyamide (PA) matrix was fabricated by doping polyamidoamine (PAMAM) dendrimers into the PA layer. This unique filling-integrated architecture endowed the RO membrane with an exceptional NH4+-N rejection of 98.39%. Mechanistically, PAMAM dendrimers optimize monomer diffusion kinetics and reaction thermodynamics during interfacial polymerization (IP), regulating the self-limiting effect to form a defect-reduced PA layer with homogenized free-volume characteristics, thereby improving size-sieving capabilities while maintaining favorable water permeability (3.74 L/m2·h·bar). Concurrently, the embedded abundant amine groups (-NH2 and R3N) undergo protonation to form highly positive charges (-NH3+ and R3NH+) within the PA layer, synergizing with the negatively charged membrane surface (-COO-) to establish a robust multiscale electrostatic barrier. This system directly repels NH4+ and indirectly enhances rejection by impeding Cl- transport via the Donnan effect. Furthermore, the structural similarity between the protonated -NH2 (-NH3+) and NH4+ ions generates a "concentration trap" within the PA layer via molecular mimicry, inducing site-specific simulation that elevates intramembrane NH4+ concentration to establish a chemical potential barrier to oppose NH4+ diffusion. The synergistic "structure-charge-concentration" mechanism intrinsic to the filling-integrated design thus effectively inhibits NH4+ migration while concurrently enabling integrated fouling resistance through optimized surface architecture and charge-regulated interfacial interactions. This study offers an advanced membrane separation technology, contributing significantly to low-carbon-water recycling and sustainable development goals.
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