Dual-phase microporous polymer nanofilms by interfacial polymerization for ultrafast molecular separation

被引:7
|
作者
Lee, Tae Hoon [1 ]
Balcik, Marcel [2 ]
Wu, Wan-Ni [1 ]
Pinnau, Ingo [2 ]
Smith, Zachary P. [1 ]
机构
[1] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[2] King Abdullah Univ Sci & Technol, Adv Membranes & Porous Mat Ctr, Chem Engn Program, Phys Sci & Engn Div, Thuwal 23955, Saudi Arabia
来源
SCIENCE ADVANCES | 2024年 / 10卷 / 33期
关键词
ORGANIC-SOLVENT NANOFILTRATION; INTRINSIC MICROPOROSITY; POLYANILINE MEMBRANES; POLYAMIDE NANOFILMS; PERFORMANCE; TRANSPORT; PERMEATION; FILMS; BASE; PIMS;
D O I
10.1126/sciadv.adp6666
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
Fine-tuning microporosity in polymers with a scalable method has great potential for energy-efficient molecular separations. Here, we report a dual-phase molecular engineering approach to prepare microporous polymer nanofilms through interfacial polymerization. By integrating two micropore-generating units such as a water-soluble Troger's base diamine (TBD) and a contorted spirobifluorene (SBF) motif, the resultant TBD-SBF polyamide shows an unprecedentedly high surface area. An ultrathin TBD-SBF membrane (similar to 20 nm) exhibits up to 220 times improved solvent permeance with a moderate molecular weight cutoff (similar to 640 g mol(-1)) compared to the control membrane prepared by conventional chemistry, which outperforms currently reported polymeric membranes. We also highlight the great potential of the SBF-based microporous polyamides for hydrocarbon separations by exploring the isomeric effects of aqueous phase monomers to manipulate microporosity.
引用
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页数:10
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