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Electrophoretic Crystallization of Ultrathin High-performance Metal-organic Framework Membranes
Published on: August 16, 2018
Scalable Art-Inspired Tessellated Covalent Organic Framework Membranes Enable Highly Selective Ion Separation
Zhenyi Zhao1,2, Rui Guo1,2, Tianxiang Yang1,2
1School of Chemical Engineering and Technology, Tianjin University, Tianjin, P. R. China.
Abstract:
Covalent organic frameworks (COFs), distinguished by their periodic and tunable network structures, exhibit great potential for molecular and ionic separation. Nevertheless, fabricating COF membranes with angstrom-scale pores faces challenges in precisely controlling channel dimensions and achieving seamless integration of frameworks. Here, we report the synthesis of a substoichiometric aminal-linked COF with a pore size of ∼5 Å and develop a covalent tessellation strategy inspired by Escher's art and derived from interfacial polymerization, that successfully fabricates defect-free tessellated COF (tCOF) membranes. The resulting tCOF membrane exhibits ultra-microporous structures, achieving high water permeance of 10.2 L m-2 h-1 bar-1, nearly perfect Na2SO4 rejection of 99.4%, and exceptional Cl-/SO4 2- selectivity of 1,090. The tCOF membranes can be continuously scaled up to roll-to-roll format with a width of 30 cm and an unlimited length. The potential applications in resource recovery are proved with a two-stage nanofiltration process, which produces NaCl with a high purity of >99% from NaCl/Na2SO4 mixtures. Therefore, the innovative covalent tessellation methodology reported in this work provides a new avenue for the development of scalable COF membranes with angstrom-scale pores for highly selective separation.
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