Preparation of inorganic-organic hybrid proton exchange membrane with chemically bound hydroxyethane diphosphonic acid

Proton‐conductive inorganic–organic hybrid intermediate‐temperature membranes were prepared from 3‐glycidoxypropyltrimethoxysilane (GPTMS) and 1‐hydroxyethane‐1,1‐diphosphonic acid (HEDPA) by sol–gel process. To prevent the leaching out of phosphonic acid, triethylamine was used as catalyst to promo...

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Bibliographic Details
Published inJournal of applied polymer science Vol. 126; no. 3; pp. 954 - 959
Main Authors Shen, Chunhui, Guo, Zhihan, Chen, Cheng, Gao, Shanjun
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 05.11.2012
Wiley
Wiley Subscription Services, Inc
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Summary:Proton‐conductive inorganic–organic hybrid intermediate‐temperature membranes were prepared from 3‐glycidoxypropyltrimethoxysilane (GPTMS) and 1‐hydroxyethane‐1,1‐diphosphonic acid (HEDPA) by sol–gel process. To prevent the leaching out of phosphonic acid, triethylamine was used as catalyst to promote the reaction of HEDPA and GPTMS to immobilize phosphonic acid groups. Fourier transform infrared spectra revealed that phosphonic acid groups of HEDPA were chemically bounded to organosiloxane network as a result of the reaction of POH of HEDPA and epoxy ring of GPTMS. TG‐DSC results indicated that the hybrid membranes were thermally stable up to 250°C. The proton conductivity of the hybrid membranes increased with temperature from 30 to 130°C. The proton conductivity of hybrid membrane with the molar ratio of GPTMS/HEDPA = 2/1 can reach up to 1.0 × 10−3 S/cm under anhydrous condition at 130°C, which reveals that this membrane is a promising proton exchange membrane for intermediate‐temperature proton exchange membrane fuel cell. © 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012
Bibliography:ark:/67375/WNG-VHX5PDM6-0
State Education Ministry (Scientific Research Foundation for the Returned Overseas Chinese Scholars)
istex:45F721CB5BF4EAB79ABF136919ECC20F7260D254
National Natural Science Foundation of China - No. 21076167
ArticleID:APP36972
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0021-8995
1097-4628
DOI:10.1002/app.36972