Synthesis and Properties of Sulfonated Polyimide/Polybenzimidazole Cross-Linked Membranes for Fuel Cell Applications

Article Preview

Abstract:

A series of cross-linked proton exchange membranes with the ion exchange capacities (IECs) of 0.70 - 1.52 meq/g have been prepared via the reaction of the anhydride-terminated sulfonated polyimide oligomers (SPI-3, SPI-5 and SPI-7, here the figure refers to the averaged block length) and the polybenzimidazole with pendant amino groups (H2N-PBI) in dimethylsulfoxide (DMSO) during the membrane cast process. The prepared cross-linked membranes showed high tensile strength (55 - 80 MPa) and good water stability (> 2 months in deionized water at 100 °C). Fenton’s test revealed that all the cross-linked membranes displayed significantly better radical oxidative stability than the corresponding pure SPIs. This is attributed to the presence of the highly oxidative-stable PBI component in the cross-linked membranes. The proton conductivities of the cross-linked membranes increased with increasing temperature and relative humidity. The cross-linked membrane prepared from the longest oligomer (SPI-7) displayed the highest proton conductivity which is comparable to that of Nafion 117.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 287-290)

Pages:

2516-2521

Citation:

Online since:

July 2011

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2011 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] Y. Yin, S. Hayashi, O. Yamada, H. Kita, K. Okamoto: Macromol. Rapid Commun. Vol. 26 (2005), p.696.

Google Scholar

[2] S. Wu, Z. Qiu, S. Zhang, X. Yang, F. Yang, Z. Li: Polymer Vol. 47 (2006), p.6993.

Google Scholar

[3] N. Endo, K. Matsuda, K. Yaguchi, Z. Hu, K. Chen, M. Higa, K. Okamoto: J. Electrochem. Soc. Vol. 156 (2009), p. B628.

DOI: 10.1149/1.3097180

Google Scholar

[4] Y. Yin, J. Fang, T. Watari, K. Tanaka, H. Kita, K. Okamoto: J. Mater. Chem. Vol. 14 (2004), p.1062.

Google Scholar

[5] N. Xu, X.Guo, J. Fang, J. Yin,M. Yuan, B. Chen: Fuel Cells Vol. 9 (2009), p.363.

Google Scholar

[6] G. Zhang, X. Guo, J. Fang, K. Chen, K. Okamoto, J. Membr. Sci. Vol. 326 (2009), p.708.

Google Scholar

[7] H. Xu, K. Chen, X. Guo, J. Fang, J. Yin: Polymer Vol. 48 (2007), p.5556.

Google Scholar

[8] J. Fang, F. Zhai, X. Guo, H. Xu, K. Okamoto: J. Mater. Chem. Vol. 17 (2007), p.1102.

Google Scholar

[9] C. Zhang, X. Guo, J. Fang, H. Xu, M. Yuan, B. Chen: J. Power Sources Vol. 170 (2007), p.42.

Google Scholar

[10] J. Fang, X. Guo, S. Harada, T. Watari, K. Tanaka, H. Kita, K. Okamoto: Macromolecules Vol. 35 (2002), p.9022.

Google Scholar

[11] N. Xu, X. Guo, J. Fang, H. Xu, J. Yin: J. Polym. Sci., Part A: Polym. Chem. Vol. 47 (2009), p.6992.

Google Scholar