| Literature DB >> 28691317 |
Nasser Alaslai1, Xiaohua Ma1, Bader Ghanem1, Yingge Wang1, Fahd Alghunaimi1, Ingo Pinnau1.
Abstract
An intrinsically microporous polyimide is synthesized in m-cresol by a one-pot high-temperature condensation reaction of 4,4'-(hexafluoroisopropylidene)diphthalic anhydride (6FDA) and newly designed 2,6 (7)-dihydroxy-3,7(6)-diaminotriptycene (DAT1-OH). The 6FDA-DAT1-OH polyimide is thermally stable up to 440 °C, shows excellent solubility in polar solvents, and has moderately high Brunauer-Teller-Emmett (BET) surface area of 160 m2 g-1 , as determined by nitrogen adsorption at -196 °C. Hydroxyl functionalization applied to the rigid 3D triptycene-based diamine building block results in a polyimide that exhibits moderate pure-gas CO2 permeability of 70 Barrer combined with high CO2 /CH4 selectivity of 50. Mixed-gas permeation studies demonstrate excellent plasticization resistance of 6FDA-DAT1-OH with impressive performance as potential membrane material for natural gas sweetening with a CO2 permeability of 50 Barrer and CO2 /CH4 selectivity of 40 at a typical natural gas well partial pressure of 10 atm.Entities:
Keywords: gas separation; hydroxyl functionalization; intrinsic microporosity; membranes; polyimide
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Year: 2017 PMID: 28691317 DOI: 10.1002/marc.201700303
Source DB: PubMed Journal: Macromol Rapid Commun ISSN: 1022-1336 Impact factor: 5.734