Polymer nanofilms with enhanced microporosity by interfacial polymerization
Highly permeable and selective membranes are desirable for energy-efficient gas and liquid separations. Microporous organic polymers have attracted significant attention in this respect owing to their high porosity, permeability and molecular selectivity. However, it remains challenging to fabricate...
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Veröffentlicht in: | Nature materials 2016-07, Vol.15 (7), p.760-767 |
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Sprache: | eng |
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Zusammenfassung: | Highly permeable and selective membranes are desirable for energy-efficient gas and liquid separations. Microporous organic polymers have attracted significant attention in this respect owing to their high porosity, permeability and molecular selectivity. However, it remains challenging to fabricate selective polymer membranes with controlled microporosity that are stable in solvents. Here we report a new approach to designing crosslinked, rigid polymer nanofilms with enhanced microporosity by manipulating the molecular structure. Ultrathin polyarylate nanofilms with thickness down to 20 nm are formed
in situ
by interfacial polymerization. Enhanced microporosity and higher interconnectivity of intermolecular network voids, as rationalized by molecular simulations, are achieved by using contorted monomers for the interfacial polymerization. Composite membranes comprising polyarylate nanofilms with enhanced microporosity fabricated
in situ
on crosslinked polyimide ultrafiltration membranes show outstanding separation performance in organic solvents, with up to two orders of magnitude higher solvent permeance than membranes fabricated with nanofilms made from non-contorted planar monomers.
Here it is shown how ultrathin and microporous polymer membranes, fabricated using sterically contorted monomers, can achieve enhanced performance for solvent-based separations. |
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ISSN: | 1476-1122 1476-4660 |
DOI: | 10.1038/nmat4638 |