Please use this identifier to cite or link to this item:
https://doi.org/10.1002/aenm.201200296
DC Field | Value | |
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dc.title | UV-rearranged PIM-1 polymeric membranes for advanced hydrogen purification and production | |
dc.contributor.author | Li, F.Y. | |
dc.contributor.author | Xiao, Y. | |
dc.contributor.author | Ong, Y.K. | |
dc.contributor.author | Chung, T.-S. | |
dc.date.accessioned | 2014-10-09T07:05:39Z | |
dc.date.available | 2014-10-09T07:05:39Z | |
dc.date.issued | 2012-12 | |
dc.identifier.citation | Li, F.Y., Xiao, Y., Ong, Y.K., Chung, T.-S. (2012-12). UV-rearranged PIM-1 polymeric membranes for advanced hydrogen purification and production. Advanced Energy Materials 2 (12) : 1456-1466. ScholarBank@NUS Repository. https://doi.org/10.1002/aenm.201200296 | |
dc.identifier.issn | 16146832 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/90470 | |
dc.description.abstract | Polymers of intrinsic microporosity (PIM-1) have been known for their super high permeability but average selectivity for medium-size gas pairs. They have unimpressive selectivity for H2 and CO2 separation (i.e., α (H2/CO2) = 0.6). For the first time, we have discovered that ultraviolet (UV)-rearranged polymers of PIM-1 membranes can be used for H2/CO2 separation with far superior separation performance to others in literatures. The PIM-1 membrane after UV radiation for 4 hours shows H2 permeability of 452 barrer with H 2/CO2 selectivity of 7.3. Experimental data and molecular simulation reveal that the polymer chains of PIM-1 undergo 1,2-migration reaction and transform to close-to-planar like rearranged structure after UV radiation. As a result, the UV-irradiated PIM-1 membrane shows considerable drops in both fractional free volume (FFV) and size of micro-pores. Positron annihilation lifetime (PAL) results have confirmed the chemical and structural changes, suggesting the FFV and pore size drops are mainly ascribed to the destructed spiro-carbon centre during UV radiation. Sorption and x-ray diffractor (XRD) analyses indicate that the impressive H2/CO 2 selectivity arises from the significantly enhanced diffusivity selectivity induced by UV radiation, followed by molecular rearrangement, conformation change and chain packing. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/aenm.201200296 | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMICAL & BIOMOLECULAR ENGINEERING | |
dc.description.doi | 10.1002/aenm.201200296 | |
dc.description.sourcetitle | Advanced Energy Materials | |
dc.description.volume | 2 | |
dc.description.issue | 12 | |
dc.description.page | 1456-1466 | |
dc.identifier.isiut | 000312035800007 | |
Appears in Collections: | Staff Publications |
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