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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2016-01-01
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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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id | doaj-art-f55f898d065741f6a99eef4b9a6eb890 |
institution | Kabale University |
issn | 1687-9422 1687-9430 |
language | English |
publishDate | 2016-01-01 |
publisher | Wiley |
record_format | Article |
series | International Journal of Polymer Science |
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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