Actions for Interplay between water uptake, ion interactions, and conductivity in an e-beam grafted poly(ethylene-co-tetrafluoroethylene) anion exchange membrane [electronic resource].
Interplay between water uptake, ion interactions, and conductivity in an e-beam grafted poly(ethylene-co-tetrafluoroethylene) anion exchange membrane [electronic resource].
- Published
- Washington, D.C. : United States. Dept. of Energy. Office of Science, 2014.
Oak Ridge, Tenn. : Distributed by the Office of Scientific and Technical Information, U.S. Dept. of Energy - Physical Description
- pages 4,367-4,378 : digital, PDF file
- Additional Creators
- Argonne National Laboratory, United States. Department of Energy. Office of Science, and United States. Department of Energy. Office of Scientific and Technical Information
Access Online
- Restrictions on Access
- Free-to-read Unrestricted online access
- Summary
- We demonstrate that the true hydroxide conductivity in an e-beam grafted poly(ethylene-co-tetrafluoroethylene) [ETFE] anion exchange membrane (AEM) is as high as 132 mS cm-1 at 80 °C and 95% RH, comparable to a proton exchange membrane, but with very much less water present in the film. To understand this behaviour we studied ion transport of hydroxide, carbonate, bicarbonate and chloride, as well as water uptake and distribution. Water uptake of the AEM in water vapor is an order of magnitude lower than when submerged in liquid water. In addition 19F pulse field gradient spin echo NMR indicates that there is little tortuosity in the ionic pathways through the film. A complete analysis of the IR spectrum of the AEM and the analyses of water absorption using FT-IR led to conclusion that the fluorinated backbone chains do not interact with water and that two types of water domains exist within the membrane. The reduction in conductivity was measured during exposure of the OH- form of the AEM to air at 95% RH and was seen to be much slower than the reaction of CO2 with OH- as the amount of water in the film determines its ionic conductivity and at relative wet RHs its re-organization is slow.
- Report Numbers
- E 1.99:1214333
- Subject(s)
- Note
- Published through SciTech Connect.
12/23/2014.
Physical Chemistry Chemical Physics. PCCP (Print) 17 6 ISSN 1463-9076; PPCPFQ AM
Pandey, Tara; Maes, Ashley; Sarode, Himanshu; Peters, Bethanne; Lavina, Sandra; Vezzù, Keti; Yang, Yuan; Poynton, Simon; Varcoe, John; Seifert, Soenke; Liberatore, Matthew; Di Noto, Vito; Herring, Andrew. - Funding Information
- AC02-06CH11357
EP/I004882/1
W911NF-11-1-0462
CHE-0923537
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