Cited by 79Fuel Cells and Related MaterialsMembrane-based Ion Separation TechniquesAdvancements in Solid Oxide Fuel Cells

Correlation of In Situ and Ex Situ Measurements of Water Permeation Through Nafion NRE211 Proton Exchange Membranes

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Adachi, Makoto, Navessin, Titichai, Xie, Zhong, Frisken, Barbara, Holdcroft, Steven·2009·Journal of The Electrochemical Society

Abstract

Water permeability at is determined for Nafion NRE211 membrane exposed to either liquid or vapor phases of water. Chemical potential gradients of water across the membrane are controlled through use of differential humidity (38–100% RH) in the case of water vapor and hydraulic pressure in the case of liquid water. Accordingly, three types of water permeation are defined: vapor-vapor permeation, liquid-vapor permeation (LVP), and liquid-liquid permeation. The difference in chemical potentials across the membrane, and more significantly, the flux of water, is largest when the membrane is exposed to liquid on one side and vapor on the other (i.e., LVP conditions). Polarization curves and net water fluxes are reported for NRE211-based MEAs at under two different operating conditions. Water permeability measurements obtained ex situ are compared to fuel cell water balance measurements obtained in situ. It is found that the magnitude of back-transport of water during fuel cell operation can be explained only by considering that the membrane is exposed to liquid on one side and vapor on the other (i.e., LVP conditions). Thus, LVP water transport is largely responsible for regulating water balance within the operating membrane electrode assembly.

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  • Adachi et al. demonstrated experimentally that allowing liquid equilibration of one face of the membrane while maintaining vapour equilibration on the other greatly increased the permeation rate compared to a vapour-vapour membrane, due to the elimination of one interfacial resistance.

    “Adachi et al. demonstrated experimentally that allowing liquid equilibration of one face of the membrane, while maintaining vapour equilibration on the other, greatly increased the permeation rate compared to a vapour–vapour membrane, due to the elimination of one interfacial resistance [126].”
  • For membranes where one face is vapour-equilibrated but the other is liquid-equilibrated, interfacial effects under a humidity gradient have been argued to dominate pressure gradient effects.

    “For the case of membranes where one face is vapour-equilibrated but the other is liquid-equilibrated, interfacial effects under a humidity gradient have been argued to dominate pressure gradient effects in other works [122,126,127].”

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Authors
Adachi, M., Navessin, T., Xie, Z., Frisken, B., & Holdcroft, S.
Affiliations
  • National Research Council Canada (CA)
  • Simon Fraser University (CA)
Venue
Journal of The Electrochemical Society
Published
2009
Volume
156
Issue
6
Pages
B782
ISSN
0013-4651 (ISSN-L)
OpenAlex
W2152159099
Cited by
79
References
1
Citations by year
2026: 4 · 2024: 5 · 2023: 3 · 2022: 10 · 2021: 1 · 2020: 4 · 2019: 3 · 2018: 4 · 2017: 6 · 2016: 5 · 2015: 4 · 2014: 5 · 2013: 3 · 2012: 5
FWCI
5.82
Type
journal article
Language
en
Open access
Locations
  • Journal of The Electrochemical Society (publishedVersion)
  • NPARC (submittedVersion)
Topics
  • Physical Sciences › Engineering › Electrical and Electronic Engineering › Fuel Cells and Related Materials
  • Physical Sciences › Chemical Engineering › Filtration and Separation › Membrane-based Ion Separation Techniques
  • Physical Sciences › Materials Science › Materials Chemistry › Advancements in Solid Oxide Fuel Cells
Keywords
proton exchange membranes, water permeability, chemical potential gradient, membrane electrode assembly, polarization curves, humidity, hydraulic pressure

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