Interfacially stable MOF nanosheet membrane with tailored nanochannels for ultrafast and thermo-responsive nanofiltration

被引:38
|
作者
Jia, Wei [1 ,2 ]
Wu, Baohu [3 ]
Sun, Shengtong [1 ]
Wu, Peiyi [1 ,2 ]
机构
[1] Donghua Univ, Coll Chem Chem Engn & Biotechnol, Ctr Adv Low Dimens Mat, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
[2] Fudan Univ, Dept Macromol Sci, State Key Lab Macromol Engn Polymers, 2205 Songhu Rd, Shanghai 200433, Peoples R China
[3] Forschungszentrum Julich, Heinz Maier Leibnitz Zentrum MLZ, Julich Ctr Neutron Sci JCNS, Lichtenbergstr 1, D-85748 Garching, Germany
基金
中国国家自然科学基金;
关键词
metal-organic framework (MOF) nanosheet membrane; thermo-responsiveness; molecular separation; infrared (IR) spectroscopy; ORGANIC-FRAMEWORK NANOSHEETS; HYDRATION BEHAVIOR; WATER PERMEATION; POLYMERS; DESIGN; IONS;
D O I
10.1007/s12274-020-2959-6
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Two-dimensional nanosheet membranes with responsive nanochannels are appealing for controlled mass transfer/separation, but limited by everchanging thicknesses arising from unstable interfaces. Herein, an interfacially stable, thermo-responsive nanosheet membrane is assembled from twin-chain stabilized metal-organic framework (MOF) nanosheets, which function via two cyclic amide-bearing polymers, thermo-responsive poly(N-vinyl caprolactam) (PVCL) for adjusting channel size, and non-responsive polyvinylpyrrolidone for supporting constant interlayer distance. Owing to the microporosity of MOF nanosheets and controllable interface wettability, the hybrid membrane demonstrates both superior separation performance and stable thermo-responsiveness. Scattering and correlation spectroscopic analyses further corroborate the respective roles of the two polymers and reveal the microenvironment changes of nanochannels are motivated by the dehydration of PVCL chains.
引用
收藏
页码:2973 / 2978
页数:6
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