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    Gas separation performance of 6FDA-based polyimides with different chemical structures

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    Type
    Article
    Authors
    Qiu, Wulin
    Xu, Liren cc
    Chen, Chien-Chiang
    Paul, Donald R.
    Koros, William J.
    KAUST Grant Number
    KUS-I1-011-21
    Date
    2013-10
    Permanent link to this record
    http://hdl.handle.net/10754/598395
    
    Metadata
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    Abstract
    This work reports the gas separation performance of several 6FDA-based polyimides with different chemical structures, to correlate chemical structure with gas transport properties with a special focus on CO2 and CH 4 transport and plasticization stability of the polyimides membranes relevant to natural gas purification. The consideration of the other gases (He, O2 and N2) provided additional insights regarding effects of backbone structure on detailed penetrant properties. The polyimides studied include 6FDA-DAM, 6FDA-mPDA, 6FDA-DABA, 6FDA-DAM:DABA (3:2), 6FDA-DAM:mPDA (3:2) and 6FDA-mPDA:DABA (3:2). Both pure and binary gas permeation were investigated. The packing density, which is tunable by adjusting monomer type and composition of the various samples, correlated with transport permeability and selectivity. The separation performance of the polyimides for various gas pairs were also plotted for comparison to the upper bound curves, and it was found that this family of materials shows attractive performance. The CO 2 plasticization responses for the un-cross-linked polyimides showed good plasticization resistance to CO2/CH4 mixed gas with 10% CO2; however, only the cross-linked polyimides showed good plasticization resistance under aggressive gas feed conditions (CO 2/CH4 mixed gas with 50% CO2 or pure CO 2). For future work, asymmetric hollow fibers and carbon molecular sieve membranes based on the most attractive members of the family will be considered. © 2013 Elsevier Ltd. All rights reserved.
    Citation
    Qiu W, Xu L, Chen C-C, Paul DR, Koros WJ (2013) Gas separation performance of 6FDA-based polyimides with different chemical structures. Polymer 54: 6226–6235. Available: http://dx.doi.org/10.1016/j.polymer.2013.09.007.
    Sponsors
    This research was supported by the U.S. Department of Energy Grant DE-FG02-04ER15510, and was supported in part by Award No. KUS-I1-011-21, made by King Abdullah University of Science and Technology (KAUST).
    Publisher
    Elsevier BV
    Journal
    Polymer
    DOI
    10.1016/j.polymer.2013.09.007
    ae974a485f413a2113503eed53cd6c53
    10.1016/j.polymer.2013.09.007
    Scopus Count
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