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Disulfonated poly(arylene ether) and polyimide copolymers can phase separate to form nanoscale hydrophilic and hydrophobic domain morphology. Water in these domains has been assigned to three different states, tightly bound, loosely bound and free water. The states of water were characterized using DSC, NMR relaxation and TGA. The chemical structures of the proton exchange membranes were varied in...
Multiblock copolymers based on poly(arylene ether sulfone) and polybenzimidazole (PBI) with different block lengths were synthesized by coupling carboxyl functional aromatic poly(arylene ethers) with ortho diamino functional PBI oligomers in NMP, selectively doped with phosphoric acid, and evaluated as a high temperature proton exchange membrane (PEM). Transparent and ductile membranes were produced...
tert-Butylphenyl-terminated disulfonated poly(arylene ether sulfone) random copolymers with a sulfonation degree of 35mol% (BPS35) and controlled molecular weights (M n ), 20–50kgmol −1 , were successfully prepared by direct copolymerization of the two activated halides, 4,4′-dichlorodiphenyl sulfone (DCDPS) and 3,3′-disulfonate-4,4′-dichlorodiphenyl sulfone (SDCDPS) with 4,4′-biphenol...
There has been growing evidence, both experimental and theoretical, that block copolymer systems with well-defined sulfonated regions may provide enhanced proton transport, especially at low relative humidity. We have recently demonstrated a novel way to make hydrocarbon hydrophobic–hydrophilic block copolymers. While the chemical structure and chemical compositions are very similar to random copolymers,...
Biphenol-based, partially disulfonated poly(arylene ether sulfone)s synthesized by direct copolymerization show promise as potential reverse osmosis membranes. They have excellent chlorine resistance over a wide range of pHs and good anti-protein and anti-oily water fouling behavior. Crosslinking of these copolymers that have high degrees of disulfonation may improve salt rejection of the membranes...
Two series of multiblock copolymers based on poly(arylene ether sulfone)s were developed and evaluated for use as proton exchange membranes (PEMs). The multiblock copolymers were synthesized by a coupling reaction between phenoxide terminated fully disulfonated poly(arylene ether sulfone) (BPSH100) and decafluorobiphenyl (DFBP) or hexafluorobenzene (HFB) end-capped unsulfonated poly(arylene ether...
tert-Butylphenyl terminated disulfonated poly(arylene ether sulfone) copolymers with controlled molecular weights (M n ), 20–50kgmol −1 , were successfully prepared by direct copolymerization of the two activated halides, biphenol and the endcapper, 4-tert-butylphenol. The high molecular weight copolymer (molecular weight over 80kgmol −1 ) was also synthesized with 1:1 stoichiometry...
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