Abstract

Membranes that contain a high fraction of amorphous poly(ethylene glycol) (PEG) are attractive for selective removal of CO2 from H2 streams, but crystallization of PEG chains restricts both flux and selectivity. The high thickness of solution-cast membranes also limits flux. This study demonstrates the formation of composite, PEG-containing membranes through atom transfer radical polymerization of poly(ethylene glycol methyl ether methacrylate) from initiator-modified, porous substrates. The resulting membrane skins are only 50−500 nm thick, and copolymers that contain a mixture of short and long PEG side chains do not readily crystallize. The smaller PEG chains (8−9 ethylene oxide units) prevent crystallization, while the presence of longer side chains (23−24 ethylene oxide units) allows the membranes to maintain a CO2/H2 selectivity of 12 at room temperature. This work examines the effect of side-chain length on polymerization rate as well as the permeability, selectivity, and crystallinity of copolymer...

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.