Abstract
Due to the expectation that partially fluorinated arylene main-chain ionomers should have better chemical and thermal stabilities than the F-free ionomers, because of the much higher stability of C–F bonds, compared to that of C–H bonds, novel partially fluorinated and sulfonated poly(arylenethioether)s and poly(aryleneether)s were successfully synthesized via nucleophilic polycondensation of 2,3,5,6-tetrafluoropyridine-4-sulfonic acid or 2,3,5,6-tetrafluoro(trifluoromethyl)sulfonic acid with 4,4′-thiobisbenzenethiol (TBBT) or 4,4′-dihydroxybiphenol (BP-OH). All these polymers were analyzed in terms of their thermal stability. Both the novel poly(arylenethioether)s and poly(aryleneether)s were characterized by gel permeation chromatography (GPC). The poly(arylenethioether)s and poly(aryleneether)s were blended with PBI-Celazol to yield base-excess blend membranes. The base-excess blend membranes were doped with H3PO4. All membranes were analyzed in terms of their thermal and oxidative stability in 5% H2O2 solutions. Moreover the blend membranes were characterized by gel permeation chromatography (GPC) before and after the oxidation procedure to get insight into the degradation process. The novel poly(arylenethioether) blend showed excellent thermal stabilities, indicated by a quite high onset temperature of splitting-off of the sulfonic acid group (TSO3Honset) of 442°C.
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