SYNTHESIS AND PROPERTIES OF SULFONATED POLY(ARYLENE ETHER) CONTAINING TRIPHENYL METHANE MOIETIES FROM ISOCYNATE MASKED BISPHENOL
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SYNTHESIS AND PROPERTIES OF SULFONATED POLY(ARYLENE ETHER) CONTAINING TRIPHENYL METHANE MOIETIES FROM ISOCYNATE MASKED BISPHENOL
Issue 4, Pages: 419-426(2007)
Affiliations:
1. College of Material Science Shenzhen University and Shenzhen Key Laboratory of Special Functional Materials
2. Shenzhen 518060
3. China
Author bio:
Funds:
This work was financially supported by the National Science Foundation of China (NSFC) (Key project, No. 29734120)();the China High-Tech Development 863 Program (No. 2003AA302410)();Natural Science Foundation of Guangdong Province (Excellent Team Project, No. 015007)();Canton Province Sci & Tech Bureau (Key Strategic Project, No. A1100402) and Guangzhou Sci & Tech Bureau()
DOI:
CLC:O631.3
Published:2007
Accepted:
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[1]王雷.SYNTHESIS AND PROPERTIES OF SULFONATED POLY(ARYLENE ETHER) CONTAINING TRIPHENYL METHANE MOIETIES FROM ISOCYNATE MASKED BISPHENOL[J].Chinese Journal of Polymer Science,2007(04):419-426.
SYNTHESIS AND PROPERTIES OF SULFONATED POLY(ARYLENE ETHER) CONTAINING TRIPHENYL METHANE MOIETIES FROM ISOCYNATE MASKED BISPHENOL[J]. 2007, (4): 419-426.
[1]王雷.SYNTHESIS AND PROPERTIES OF SULFONATED POLY(ARYLENE ETHER) CONTAINING TRIPHENYL METHANE MOIETIES FROM ISOCYNATE MASKED BISPHENOL[J].Chinese Journal of Polymer Science,2007(04):419-426.DOI:
SYNTHESIS AND PROPERTIES OF SULFONATED POLY(ARYLENE ETHER) CONTAINING TRIPHENYL METHANE MOIETIES FROM ISOCYNATE MASKED BISPHENOL[J]. 2007, (4): 419-426.DOI:
SYNTHESIS AND PROPERTIES OF SULFONATED POLY(ARYLENE ETHER) CONTAINING TRIPHENYL METHANE MOIETIES FROM ISOCYNATE MASKED BISPHENOL
<正>A novel sulfonated poly(arylene ether) containing triphenylmethane moieties was synthesized by the sulfonation of a designed parent polymer using chlorosulfonic acid as sulfonation agent. The sulfonation took place at the para position of the pendant phenyl rings because of the specially designed parent polymer. The position and degree of sulfonation were characterized by 1H-NMR and elemental analysis. The sulfonated polymers are highly soluble in common organic solvents
such as dimethylsulfoxide
N
N’-dimethylacetamide
dimethylformamide
ethylene glycol monomethyl ether
and can be readily cast into tough and smooth films from solutions. The films showed good thermal and hydrolysis stabilities. Moreover
Fenton’s reagent test revealed that the films exhibited superior stability to oxidation. The proton conductivities of the films were comparable with Nafion 117 under same conditions. The membrane electrode assembly (MEA) prepared with the asmade film (706 EW
100μm dry thickness) shows better cell performance than Nafion 115-MEA in the whole current density range.
Abstract
A novel sulfonated poly(arylene ether) containing triphenylmethane moieties was synthesized by the sulfonation of a designed parent polymer using chlorosulfonic acid as sulfonation agent. The sulfonation took place at the para position of the pendant phenyl rings because of the specially designed parent polymer. The position and degree of sulfonation were characterized by 1H-NMR and elemental analysis. The sulfonated polymers are highly soluble in common organic solvents
such as dimethylsulfoxide
N
N’-dimethylacetamide
dimethylformamide
ethylene glycol monomethyl ether
and can be readily cast into tough and smooth films from solutions. The films showed good thermal and hydrolysis stabilities. Moreover
Fenton’s reagent test revealed that the films exhibited superior stability to oxidation. The proton conductivities of the films were comparable with Nafion 117 under same conditions. The membrane electrode assembly (MEA) prepared with the asmade film (706 EW
100μm dry thickness) shows better cell performance than Nafion 115-MEA in the whole current density range.
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