膜
化学工程
化学
聚酰胺
反渗透
界面聚合
树枝状大分子
单体
结垢
膜污染
质子化
胺气处理
选择性
铵
聚电解质
膜技术
聚合
表面改性
高分子化学
正渗透
复合数
磁导率
薄膜复合膜
图层(电子)
色谱法
离子交换
多孔性
离子
渗透
半透膜
离子强度
材料科学
作者
YI Yu-ling,Ke-Xin Yuan,Siming Xie,Xin Li,Wei Wang,Haoran Feng,Xian Bao,Jun Ma
标识
DOI:10.1021/acs.est.5c10965
摘要
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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