纳滤
膜
共价键
渗透
氢氧化钾
材料科学
化学工程
溶剂
分子
水解
高分子化学
有机化学
Knoevenagel冷凝
小分子
耐化学性
膜技术
氢氧化物
化学
缩合反应
化学改性
苯甲醛
氢氧化钠
乙酸乙酯
作者
Jiaxin Lv,Ning Chen,Zhiwei Zhao,Yimeng Wang,Yushu Sui,Yixuan Liu,Liangyu Wu,Anqi Dou,Yanyu Zhu,Ruiyang Chen,Jinhui Pang,Ning Cao
标识
DOI:10.1002/adfm.202519173
摘要
Abstract Conventional reversible covalent bonds in covalent organic frameworks (COFs) are prone to hydrolytic degradation under harsh conditions, compromising their stability. This work addresses this by replacing them with irreversible, high‐energy ethylene linkages. Herein, highly crystalline ethylene‐bridged 2D COFs membranes are synthesized via Knoevenagel condensation between benzaldehyde and 2,4,6‐trimethylpyridine. Using an economical potassium hydroxide catalyst, the process yields COFs with well‐defined pores, high specific surface areas, and remarkable crystallinity. The resulting TFB TMP‐COFs demonstrate a high pure water permeance of 248 L·m −2 ·h −1 ·bar −1 , a good salt/dye separation factor of 16.33, and superior molecular sieving capabilities. These membranes reject over 90% of active pharmaceutical ingredients and over 95% of dye molecules. Furthermore, the TFB TMP‐COFs composite membranes exhibit excellent chemical stability, even in strong acids and organic solvents like tetrahydrofuran, methanol, and ethanol. Crucially, they show significantly enhanced solvent resistance compared to commercial P84 membranes. This work establishes a foundation for employing highly crystalline and ultra‐stable vinyl‐bridged COFs nanofiltration membranes in organic small molecule purification.
科研通智能强力驱动
Strongly Powered by AbleSci AI