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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:
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.
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页数:10
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