纳滤
膜
选择性
化学工程
材料科学
界面聚合
胺气处理
磁导率
溶剂
多孔性
化学
聚合物
有机化学
单体
催化作用
生物化学
工程类
作者
Tiefan Huang,Basem Moosa,Phuong Mai Hoang,Jiangtao Liu,Ştefan Chişcă,Gengwu Zhang,Mram Alyami,Niveen M. Khashab,Suzana P. Nunes
标识
DOI:10.1038/s41467-020-19404-6
摘要
Engineering membranes for molecular separation in organic solvents is still a big challenge. When the selectivity increases, the permeability tends to drastically decrease, increasing the energy demands for the separation process. Ideally, organic solvent nanofiltration membranes should be thin to enhance the permeant transport, have a well-tailored nanoporosity and high stability in harsh solvents. Here, we introduce a trianglamine macrocycle as a molecular building block for cross-linked membranes, prepared by facile interfacial polymerization, for high-performance selective separations. The membranes were prepared via a two-in-one strategy, enabled by the amine macrocycle, by simultaneously reducing the thickness of the thin-film layers (<10 nm) and introducing permanent intrinsic porosity within the membrane (6.3 Å). This translates into a superior separation performance for nanofiltration operation, both in polar and apolar solvents. The hyper-cross-linked network significantly improved the stability in various organic solvents, while the amine host macrocycle provided specific size and charge molecular recognition for selective guest molecules separation. By employing easily customized molecular hosts in ultrathin membranes, we can significantly tailor the selectivity on-demand without compromising the overall permeability of the system.
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