Proton conducting composite membranes based on sulfonated polysulfone and polysulfone-g-(phosphonated polystyrene) via controlled atom-transfer radical polymerization for fuel cell applications
Polysulfone-g-(phosphonated polystyrene) (PPSF) is synthesized by grafting of poly(phosphonated polystyrene) to polysulfone (PSF) backbone via controlled atom-transfer radical polymerization (ATRP). And its comprehensive performances are improved by compositing with sulfonated polysulfone (SPSF). Th...
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Published in: | Solid state ionics Vol. 338; pp. 103 - 112 |
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Main Authors: | , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Amsterdam
Elsevier B.V
01-10-2019
Elsevier BV |
Subjects: | |
Online Access: | Get full text |
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Summary: | Polysulfone-g-(phosphonated polystyrene) (PPSF) is synthesized by grafting of poly(phosphonated polystyrene) to polysulfone (PSF) backbone via controlled atom-transfer radical polymerization (ATRP). And its comprehensive performances are improved by compositing with sulfonated polysulfone (SPSF). The best comprehensive performances are achieved in the composite membrane consisting of 80 wt% PPSF and 20 wt% SPSF (P80S20). The maximum proton conductivity reaches 17.23 mS cm−1 at 95 °C and 90% RH, which is 3.3 times as high as the pristine PPSF at 5.22 mS cm−1. In addition, the composite membrane exhibits favorable thermal stability, compromised water uptake and swelling ratio, significantly improved mechanical strength. Moreover, the methanol permeability is reduced from 5.74 × 10−8 cm2 s−1 for PPSF to 0.96 × 10−8 cm2 s−1 for P80S20.
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•PPSF graft copolymer is synthesized via atom transfer radical polymerization (ATRP).•PPSF/SPSF composite membrane is prepared and exhibits improved proton conductivity and other characteristics.•PPSF/SPSF composite membrane exhibits favorable thermal stability, compromised water uptake and improved mechanical strength.•PPSF/SPSF composite shows hydrogen bonding interactions between phosphonic and sulfonic groups. |
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ISSN: | 0167-2738 1872-7689 |
DOI: | 10.1016/j.ssi.2019.05.012 |