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将人工水通道无缝整合到无缺陷聚酰胺膜中用于微咸水脱盐。

Seamless incorporation of artificial water channels in defect-free polyamide membrane for desalination of brackish water.

作者信息

Liu Yingsong, Xu Xieyang, Wang Chenshuo, Yu Huijun, Wang Weiyi, Gong Yanxi, Zhao Changwei, Wang Jianbing

机构信息

School of Chemical and Environmental Engineering, China University of Mining and Technology-Beijing, Beijing, China.

College of Resources and Environmental Sciences, China Agricultural University, Beijing, China.

出版信息

Nat Commun. 2025 May 13;16(1):4439. doi: 10.1038/s41467-025-59726-x.

Abstract

Artificial water channels (AWCs) show the potential for overcoming the permeability-selectivity tradeoff of polyamide (PA) membranes. However, the availability of biomimetic materials and limitations posed by fabrication-induced defects make the development of AWC-PA membranes a daunting task. Herein, we synthesize imidazolylethyl-ureidoethyl-phenyl (IUP) compounds to form AWC by self-assembling and provide a strategy to seamlessly incorporate AWC in defect-free PA membranes. IUP compounds are molecularly designed with enhanced nature to form AWC due to π-π stacking interactions. In addition, nanosized colloid AWC aggregates can be obtained in water directly with the aid of sodium dodecyl sulfate (SDS) and conveniently incorporated into PA layers. The AWC not only promotes the preferential selective passage of water but also exhibits good compatibility with the surrounding PA matrix. The biomimetic membranes demonstrate a water permeance of 4.3 L·m·h·bar and NaCl rejection of 99.3%, much higher than that observed with marketed state-of-the-art membranes. Mechanism understanding reveals that the compatible interaction between AWC, SDS and PA matrix is a necessary requisite to fabricate defect-free AWC-PA layers. This strategy can be easily extended to industrial scale and the biomimetic membranes may represent the development direction of the next generation of high-performance reverse osmosis membranes.

摘要

人工水通道(AWC)显示出克服聚酰胺(PA)膜渗透选择性权衡的潜力。然而,仿生材料的可用性以及制造引起的缺陷所带来的限制使得AWC-PA膜的开发成为一项艰巨的任务。在此,我们合成咪唑基乙基-脲基乙基-苯基(IUP)化合物,通过自组装形成AWC,并提供一种将AWC无缝整合到无缺陷PA膜中的策略。IUP化合物通过分子设计增强了性质,由于π-π堆积相互作用而形成AWC。此外,借助十二烷基硫酸钠(SDS)可直接在水中获得纳米级胶体AWC聚集体,并方便地掺入PA层中。AWC不仅促进水的优先选择性通过,而且与周围的PA基质表现出良好的相容性。仿生膜表现出4.3 L·m·h·bar的水渗透率和99.3%的NaCl截留率,远高于市售的最先进膜。机理研究表明,AWC、SDS和PA基质之间的相容相互作用是制备无缺陷AWC-PA层的必要条件。该策略可轻松扩展到工业规模,仿生膜可能代表下一代高性能反渗透膜的发展方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75b2/12075505/ec13c2f144e0/41467_2025_59726_Fig1_HTML.jpg

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