Synthesis of Highly Sulfonated Poly(arylene ether) Containing Multiphenyl for Proton Exchange Membrane Materials

A series of sterically hindered, sulfonated, poly(arylene ether) polymers were synthesized by nucleophilic polycondensation reaction using 4,4′′′′-difluoro-3,3′′′′-bistrifluoromethyl-2′′,3′′,5′′,6′′-tetraphenyl-[1,1′;4′,1′′;4′′,1′′′;4′′′,1′′′′]-pentaphenyl and 4,4′-biphenol and were prepared through...

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Main Authors: Yi-Chiang Huang, Ruei-Hong Tai, Hsu-Feng Lee, Po-Hsun Wang, Ram Gopal, Chun-Che Lee, Mei-Ying Chang, Wen-Yao Huang
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:International Journal of Polymer Science
Online Access:http://dx.doi.org/10.1155/2016/6545362
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author Yi-Chiang Huang
Ruei-Hong Tai
Hsu-Feng Lee
Po-Hsun Wang
Ram Gopal
Chun-Che Lee
Mei-Ying Chang
Wen-Yao Huang
author_facet Yi-Chiang Huang
Ruei-Hong Tai
Hsu-Feng Lee
Po-Hsun Wang
Ram Gopal
Chun-Che Lee
Mei-Ying Chang
Wen-Yao Huang
author_sort Yi-Chiang Huang
collection DOAJ
description A series of sterically hindered, sulfonated, poly(arylene ether) polymers were synthesized by nucleophilic polycondensation reaction using 4,4′′′′-difluoro-3,3′′′′-bistrifluoromethyl-2′′,3′′,5′′,6′′-tetraphenyl-[1,1′;4′,1′′;4′′,1′′′;4′′′,1′′′′]-pentaphenyl and 4,4′-biphenol and were prepared through postpolymerization sulfonation. The chemical structures were confirmed by 1H NMR. Subsequent to sulfonation, solvent-casting membranes were provided ion exchange capacity (IEC) values ranging from 0.39 to 2.90 mmol/g. Proton conductivities of membranes ranged from 143 to 228 mS/cm at 80°C under fully humidified conditions which were higher than that of Nafion 117. The membrane also exhibited considerably dimension stability, oxidative stability, and hydrolytic stability. The microphase structure was investigated by transmission electron microscopy (TEM) and the ionic aggregation of sulfonic acid groups exhibited spherical ionic clusters with well-developed phase separated morphology. The results indicated that the membranes are promising candidates for application as proton exchange membranes. This investigation demonstrates introducing multiphenylated moieties to create a high free volume polymer that provides dimensionally stable and high proton conductivity membranes.
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institution Kabale University
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spelling doaj-art-f55f898d065741f6a99eef4b9a6eb8902025-02-03T05:58:37ZengWileyInternational Journal of Polymer Science1687-94221687-94302016-01-01201610.1155/2016/65453626545362Synthesis of Highly Sulfonated Poly(arylene ether) Containing Multiphenyl for Proton Exchange Membrane MaterialsYi-Chiang Huang0Ruei-Hong Tai1Hsu-Feng Lee2Po-Hsun Wang3Ram Gopal4Chun-Che Lee5Mei-Ying Chang6Wen-Yao Huang7Department of Photonics, National Sun Yat-Sen University, No. 70, Lienhai Road, Kaohsiung 80424, TaiwanDepartment of Photonics, National Sun Yat-Sen University, No. 70, Lienhai Road, Kaohsiung 80424, TaiwanDepartment of Photonics, National Sun Yat-Sen University, No. 70, Lienhai Road, Kaohsiung 80424, TaiwanDepartment of Photonics, National Sun Yat-Sen University, No. 70, Lienhai Road, Kaohsiung 80424, TaiwanDepartment of Photonics, National Sun Yat-Sen University, No. 70, Lienhai Road, Kaohsiung 80424, TaiwanDepartment of Photonics, National Sun Yat-Sen University, No. 70, Lienhai Road, Kaohsiung 80424, TaiwanDepartment of Photonics, National Sun Yat-Sen University, No. 70, Lienhai Road, Kaohsiung 80424, TaiwanDepartment of Photonics, National Sun Yat-Sen University, No. 70, Lienhai Road, Kaohsiung 80424, TaiwanA series of sterically hindered, sulfonated, poly(arylene ether) polymers were synthesized by nucleophilic polycondensation reaction using 4,4′′′′-difluoro-3,3′′′′-bistrifluoromethyl-2′′,3′′,5′′,6′′-tetraphenyl-[1,1′;4′,1′′;4′′,1′′′;4′′′,1′′′′]-pentaphenyl and 4,4′-biphenol and were prepared through postpolymerization sulfonation. The chemical structures were confirmed by 1H NMR. Subsequent to sulfonation, solvent-casting membranes were provided ion exchange capacity (IEC) values ranging from 0.39 to 2.90 mmol/g. Proton conductivities of membranes ranged from 143 to 228 mS/cm at 80°C under fully humidified conditions which were higher than that of Nafion 117. The membrane also exhibited considerably dimension stability, oxidative stability, and hydrolytic stability. The microphase structure was investigated by transmission electron microscopy (TEM) and the ionic aggregation of sulfonic acid groups exhibited spherical ionic clusters with well-developed phase separated morphology. The results indicated that the membranes are promising candidates for application as proton exchange membranes. This investigation demonstrates introducing multiphenylated moieties to create a high free volume polymer that provides dimensionally stable and high proton conductivity membranes.http://dx.doi.org/10.1155/2016/6545362
spellingShingle Yi-Chiang Huang
Ruei-Hong Tai
Hsu-Feng Lee
Po-Hsun Wang
Ram Gopal
Chun-Che Lee
Mei-Ying Chang
Wen-Yao Huang
Synthesis of Highly Sulfonated Poly(arylene ether) Containing Multiphenyl for Proton Exchange Membrane Materials
International Journal of Polymer Science
title Synthesis of Highly Sulfonated Poly(arylene ether) Containing Multiphenyl for Proton Exchange Membrane Materials
title_full Synthesis of Highly Sulfonated Poly(arylene ether) Containing Multiphenyl for Proton Exchange Membrane Materials
title_fullStr Synthesis of Highly Sulfonated Poly(arylene ether) Containing Multiphenyl for Proton Exchange Membrane Materials
title_full_unstemmed Synthesis of Highly Sulfonated Poly(arylene ether) Containing Multiphenyl for Proton Exchange Membrane Materials
title_short Synthesis of Highly Sulfonated Poly(arylene ether) Containing Multiphenyl for Proton Exchange Membrane Materials
title_sort synthesis of highly sulfonated poly arylene ether containing multiphenyl for proton exchange membrane materials
url http://dx.doi.org/10.1155/2016/6545362
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