Novel Sulfonated Polyimides as Polyelectrolytes for Fuel Cell Application. 1. Synthesis, Proton Conductivity, and Water Stability of Polyimides from 4,4‘-Diaminodiphenyl Ether-2,2‘-disulfonic Acid | doi.page

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Novel Sulfonated Polyimides as Polyelectrolytes for Fuel Cell Application. 1. Synthesis, Proton Conductivity, and Water Stability of Polyimides from 4,4‘-Diaminodiphenyl Ether-2,2‘-disulfonic Acid

Macromolecules2002Vol. 35(24), pp. 9022–9028

Citations Over TimeTop 1% of 2002 papers

Jianhua Fang, Xiaoxia Guo, Satoshi Harada, Tatsuya Watari, Kazuhiro Tanaka, Hidetoshi Kita, Ken‐ichi Okamoto

Abstract

A sulfonated diamine monomer, 4,4‘-diaminodiphenyl ether-2,2‘-disulfonic acid (ODADS), was successfully synthesized by direct sulfonation of a commercially available diamine, 4,4‘-diaminodiphenyl ether (ODA), using fuming sulfuric acid as the sulfonating reagent. A series of sulfonated polyimides were prepared from 1,4,5,8-naphthalenetetracarboxylic dianhydride (NTDA), ODADS, and common nonsulfonated diamines. The resulting sulfonated polyimides displayed much better stability toward water than those derived from the widely used sulfonated diamine 2,2‘-benzidinedisulfonic acid (BDSA). This is because ODADS-based polyimide membranes have a more flexible structure than the corresponding BDSA-based ones. Fenton's reagent test revealed that ODADS-based polyimide membranes also had fair good stability to oxidation. Polyimide membranes with good water stability as well as high proton conductivity were developed. NTDA−ODADS/BAPB(1/1) copolyimide membrane (BAPB refers to 4,4‘-bis(4-aminophenoxy)biphenyl)), for example, did not lose mechanical properties after being soaked in water at 80 °C for 200 h, while its proton conductivity was still at a high level (comparable to that of Nafion 117).

Citations Over TimeTop 1% of 2002 papers

Abstract

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