Interfacial Polymerization at the Alkane/Ionic Liquid Interface

被引:161
作者
Liu, Chang [1 ]
Yang, Jing [2 ]
Guo, Bian-Bian [1 ]
Agarwal, Seema [3 ]
Greiner, Andreas [3 ]
Xu, Zhi-Kang [1 ,4 ]
机构
[1] Zhejiang Univ, Dept Polymer Sci & Engn, Key Lab Adsorpt & Separat Mat & Technol Zhejiang, MOE Key Lab Macromol Synth & Funct, Hangzhou 310027, Peoples R China
[2] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Hangzhou 310036, Peoples R China
[3] Univ Bayreuth, Macromol Chem & Bavarian Polymer Inst, Univ Str 30, D-95440 Bayreuth, Germany
[4] Zhejiang Univ, Coll Chem & Biol Engn, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金;
关键词
interfacial polymerization; ionic liquids; membranes; nanofilms; polyamides; NANOFILTRATION; MEMBRANE; NANOFILMS; TRANSPORT;
D O I
10.1002/anie.202103555
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polymerization at the liquid-liquid interface has attracted much attention for synthesizing ultrathin polymer films for molecular sieving. However, it remains a major challenge to conduct this process outside the alkane-water interface since it not only suffers water-caused side reactions but also is limited to water-soluble monomers. Here, we report the interfacial polymerization at the alkane/ionic liquid interface (IP@AILI) where the ionic liquid acts as the universal solvent for diversified amines to synthesize task-specific polyamide nanofilms. We propose that IP@AILI occurs when acyl chloride diffuses from the alkane into the ionic liquid instead of being triggered by the diffusion of amines as in the conventional alkane-water system, which is demonstrated by thermodynamic partitioning and kinetic monitoring. The prepared polyamide nanofilms with precisely adjustable pore sizes display unprecedented permeability and selectivity in various separation processes.
引用
收藏
页码:14636 / 14643
页数:8
相关论文
共 33 条
[1]  
Ameloot R, 2011, NAT CHEM, V3, P382, DOI [10.1038/NCHEM.1026, 10.1038/nchem.1026]
[2]  
[Anonymous], 2020, ANGEW CHEM, V132, P22024
[3]  
[Anonymous], 2002, ANGEW CHEM-GER EDIT, V114, P2895
[4]   CO2 capture by a task-specific ionic liquid [J].
Bates, ED ;
Mayton, RD ;
Ntai, I ;
Davis, JH .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (06) :926-927
[5]  
Baumann E., 1886, Ber. Dtsch. Chem. Ges, V19, P3218, DOI DOI 10.1002/CBER.188601902348
[6]   Spectacular Rate Enhancement of the Diels-Alder Reaction at the Ionic Liquid/n-Hexane Interface [J].
Beniwal, Vijay ;
Manna, Arpan ;
Kumar, Anil .
CHEMPHYSCHEM, 2016, 17 (13) :1969-1972
[7]  
Berthier J., 2013, MICRODROPS DIGITAL M, V2nd ed., P225, DOI [10.1016/B978-1-4557-2550-2.00005-5, DOI 10.1016/B978-1-4557-2550-2.00005-5]
[8]  
Branco LC, 2002, ANGEW CHEM INT EDIT, V41, P2771, DOI 10.1002/1521-3773(20020802)41:15<2771::AID-ANIE2771>3.0.CO
[9]  
2-U
[10]   Unravelling the solvent flux behaviour of ceramic nanofiltration and ultrafiltration membranes [J].
Buekenhoudt, A. ;
Bisignano, F. ;
De Luca, G. ;
Vandezande, P. ;
Wouters, M. ;
Verhulst, K. .
JOURNAL OF MEMBRANE SCIENCE, 2013, 439 :36-47