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Issue 16, 2019
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Constructing channel-mediated facilitated transport membranes by incorporating covalent organic framework nanosheets with tunable microenvironments

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Abstract

Inspired by the efficient facilitated diffusion via carrier proteins in biological membranes, facilitated transport membranes with synthetic carriers have been fabricated to enhance the separation performance via carrier-penetrant reversible reactions. Constructing highly ordered channels for the facilitated transport process in such membranes is favorable for achieving high efficiency, but reports are quite rare. Herein, crystalline porous covalent organic framework nanosheets (CONs) with regular pore structures, were used to load transition metal ions (typical carriers for unsaturated molecules) on their pore wall to enable a facilitated transport process in ordered channels. The physicochemical properties of the channels were elucidated by the CON microenvironments including the physical microenvironment (pore size) and the chemical microenvironment (carrier amount and carrier type). The microenvironment–performance relationship of the membranes was explored. The optimized facilitated transport membranes exhibited promising separation performance for gasoline desulfurization with a permeation flux of 21.6 kg m−2 h−1 and an enrichment factor of 6.29. Long-term operational stability and enhanced anti-swelling properties manifested superior stability of the resulting membranes.

Graphical abstract: Constructing channel-mediated facilitated transport membranes by incorporating covalent organic framework nanosheets with tunable microenvironments

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Supplementary files

Article information


Submitted
10 Dec 2018
Accepted
19 Mar 2019
First published
19 Mar 2019

J. Mater. Chem. A, 2019,7, 9912-9923
Article type
Paper

Constructing channel-mediated facilitated transport membranes by incorporating covalent organic framework nanosheets with tunable microenvironments

M. Wang, F. Pan, H. Yang, Y. Cao, H. Wang, Y. Song, Z. Lu, M. Sun, H. Wu and Z. Jiang, J. Mater. Chem. A, 2019, 7, 9912
DOI: 10.1039/C8TA11883C

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