纳滤
聚酰胺
膜
界面聚合
结晶度
化学工程
无定形固体
结晶
聚合
材料科学
磁导率
生物污染
选择性
高分子化学
同种类的
纳米复合材料
表面改性
聚合物
化学
水处理
膜技术
聚丙烯
作者
Hao Zhang,J. L. Wu,Xin Cao,Jingjing Guo,Menachem Elimelech,Yunkun Wang
标识
DOI:10.1038/s41467-026-76628-8
摘要
Abstract Nanofiltration (NF) membranes are essential for water purification. However, their performance is still largely optimized through empirical methods, as polyamide crystallinity remain difficult to control in scalable interfacial polymerization processes. In this study, we introduce an ultra-low-temperature interfacial polymerization strategy at −20 °C that enables direct polyamide chain assembly, suppresses crystallization, and forms a smooth, defect-free, fully amorphous selective layer. Comprehensive characterization confirms the formation of a homogeneous amorphous network, enabling a fourfold increase in water permeability and a threefold improvement in Cl - /SO 4 2- selectivity compared with room-temperature controls, surpassing high-performance NF membranes. The smooth surface further improves the antifouling performance of the NF membrane. Life cycle assessment based on experiments with real industrial wastewater, demonstrate that using the fabricated membrane can reduce treatment costs by 79.1%. This work establishes temperature-controlled chain assembly as a scalable lever for NF design and provides a practical pathway toward next-generation membranes for water treatment.
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