Volume 132, Issue 10
Article

Durability and performance of polystyrene-b-poly(vinylbenzyl trimethylammonium) diblock copolymer and equivalent blend anion exchange membranes

Melissa A. Vandiver

Melissa A. Vandiver

Department of Chemical and Biological Engineering, Colorado School of Mines, Golden, Colorado, 80401

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Benjamin R. Caire

Benjamin R. Caire

Department of Chemical and Biological Engineering, Colorado School of Mines, Golden, Colorado, 80401

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Zach Poskin

Zach Poskin

Department of Chemical and Biological Engineering, Colorado School of Mines, Golden, Colorado, 80401

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Yifan Li

Yifan Li

Department of Chemistry and Geochemistry, Colorado School of Mines, Golden, Colorado, 80401

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Sönke Seifert

Sönke Seifert

X-Ray Science Division, Argonne National Laboratory, Argonne, Illinois, 60439

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Daniel M. Knauss

Daniel M. Knauss

Department of Chemistry and Geochemistry, Colorado School of Mines, Golden, Colorado, 80401

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Andrew M. Herring

Andrew M. Herring

Department of Chemical and Biological Engineering, Colorado School of Mines, Golden, Colorado, 80401

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Matthew W. Liberatore

Corresponding Author

Matthew W. Liberatore

Department of Chemical and Biological Engineering, Colorado School of Mines, Golden, Colorado, 80401

Correspondence to: M. W. Liberatore (E-mail: [email protected])Search for more papers by this author
First published: 01 November 2014
Citations: 26

ABSTRACT

Anion exchange membranes (AEM) are solid polymer electrolytes that facilitate ion transport in fuel cells. In this study, a polystyrene-b-poly(vinylbenzyl trimethylammonium) diblock copolymer was evaluated as potential AEM and compared with the equivalent homopolymer blend. The diblock had a 92% conversion of reactive sites with an IEC of 1.72 ± 0.05 mmol g−1, while the blend had a 43% conversion for an IEC of 0.80 ± 0.03 mmol g−1. At 50°C and 95% relative humidity, the chloride conductivity of the diblock was higher, 24–33 mS cm−1, compared with the blend, 1–6 mS cm−1. The diblock displayed phase separation on the length scale of 100 nm, while the blend displayed microphase separation (∼10 μm). Mechanical characterization of films from 40 to 90 microns thick found that elasticity and elongation decreased with the addition of cations to the films. At humidified conditions, water acted as a plasticizer to increase film elasticity and elongation. While the polystyrene-based diblock displayed sufficient ionic conductivity, the films' mechanical properties require improvement, i.e., greater elasticity and strength, before use in fuel cells. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41596.

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