Anhydrous interfacial polymerization of sub-1 Å sieving polyamide membrane

被引:68
作者
Zhao, Guangjin [1 ]
Gao, Haiqi [2 ]
Qu, Zhou [1 ]
Fan, Hongwei [1 ]
Meng, Hong [2 ]
机构
[1] Beijing Univ Chem Technol, Coll Chem Engn, Beijing 100029, Peoples R China
[2] Xinjiang Univ, Coll Chem, State Key Lab Chem & Utilizat Carbon Based Energy, Urumqi 830046, Peoples R China
基金
中国国家自然科学基金;
关键词
NANOFILTRATION MEMBRANE; FILM FORMATION; SEPARATION; TRANSPORT;
D O I
10.1038/s41467-023-43291-2
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Highly permeable polyamide (PA) membrane capable of precise ionic sieving can be utilized for many energy-efficient chemical separations. To fulfill this target, it is crucial to innovate membrane-forming process to induce a narrow pore-size distribution. Herein, we report an anhydrous interfacial polymerization (AIP) at a solid-liquid interface where the amine layer sublimated is in direct contact with the alkane containing acyl chlorides. In such a heterophase interface, water-caused side reactions are eliminated, and the amines in compact arrangement enable an intensive and orderly IP reaction, leading to a unique PA layer with an ionic sieving accuracy of 0.5 angstrom. The AIP-PA membrane demonstrates excellent separation selectivities of monovalent and divalent cations such as Mg2+/Li+ (78.3) and anions such as Cl-/SO42- (29.2) together with a high water flux up to 13.6 L m-2 h-1 bar-1. Our AIP strategy may provide inspirations for engineering high-precision PA membranes available in various advanced separations. The design of highly permeable polyamide (PA) membrane capable of precise ionic sieving remains challenging. Here, the authors report an anhydrous interfacial polymerization on the solid-liquid interface to eliminate water-caused side reactions, leading to a PA layer with an ionic sieving accuracy of 0.5 angstrom.
引用
收藏
页数:10
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