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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.
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页码:2973 / 2978
页数:6
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