2013
DOI: 10.1016/j.eurpolymj.2012.11.002
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Novel partially fluorinated sulfonated poly(arylenethioether)s and poly(aryleneether)s prepared from octafluorotoluene and pentafluoropyridine, and their blends with PBI-Celazol

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Cited by 23 publications
(14 citation statements)
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“…246 Following this, the concept has been extended to a wide range of blend systems of m-PBI and various sulfonated derivatives of e.g. poly(arylene thioether)s, 247 partially fluorinated poly(arylene(thio)ether)s 202,248,249 and poly(arylene ether sulfone) copolymers. 250 Blends of m-PBI and perfluorosulfonic acid (Nafion ® ) have been extensively studied using different cationic forms of the ionomer, and visually homogeneous blends could be obtained in the full composition range when the ammonium form was used.…”
Section: Polymer Blends and Interpenetrating Polymer Networkmentioning
confidence: 99%
“…246 Following this, the concept has been extended to a wide range of blend systems of m-PBI and various sulfonated derivatives of e.g. poly(arylene thioether)s, 247 partially fluorinated poly(arylene(thio)ether)s 202,248,249 and poly(arylene ether sulfone) copolymers. 250 Blends of m-PBI and perfluorosulfonic acid (Nafion ® ) have been extensively studied using different cationic forms of the ionomer, and visually homogeneous blends could be obtained in the full composition range when the ammonium form was used.…”
Section: Polymer Blends and Interpenetrating Polymer Networkmentioning
confidence: 99%
“…The challenge lies in efficient proton conduction with low methanol crossovers retaining the high temperature properties, sufficient oxidative stability, and mechanical strength with low water uptake at higher sulfonation degree. [103] 1-22 [105] Scheme 17 Representative structures of a sulfonated fluorinated poly(arylene ether) used for preparing blend membrane with PBI.…”
Section: Discussionmentioning
confidence: 99%
“…Initially, compound 7 was prepared by the nucleophilic thiolation of PFPy, followed by oxidation of the thiol to sulfonic acid. Next, 7 was reacted with 4.4′-thiobisbenzenethiol or 4,4′-dihydroxybiphenol to obtain a new poly(arylene thioether) or poly(arylene ether), respectively ( 8 or 9 , Scheme 11 ) [ 61 ]. Characterization of polymer 8 and 9 by 19 F NMR analysis indicated the structures shown.…”
Section: Perfluoropyridine Used In Polymers and Materialsmentioning
confidence: 99%