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Interface resistances of anion exchange membranes in microbial fuel cells with low ionic strength

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Abstract
The interface resistances between an anion exchange membrane (AEM) and the solution electrolyte were measured for low buffer (or ionic strength) of electrolytes typical of microbial fuel cells (MFCs). Three AEMs (AFN, AM-1, and ACS) having different properties were tested in a flat-plate MFC to which 5-mM acetate was fed to the anode and an air-saturated phosphate buffer (PB) solution was fed to the cathode. Current density achieved in the MFCs was correlated inversely with independently measured membrane-only resistances. However, the total interfacial resistances measured by current-voltage plots were approximately two orders higher than those of the membrane-only resistances, although membranes had the same order as with the membrane-only resistance. EIS spectra showed that the resistances from electric-double layer and diffusion boundary layer were the main resistances not the membrane's resistance. The electric-double layer and diffusion boundary layer resistances of the AEMs were much larger in the 10 mM PB electrolyte, compared to 100 mM PB. EIS study also showed that the resistance of diffusion boundary layer decreased due to mechanical stirring. Therefore, the interface resistance that originates from the interaction between the membrane and the catholyte solution should be considered when designing and operating MFC processes with an AEM. The AEMs allowed transport of uncharged O(2) and acetate, but the current losses for both were low during normal MFC operation. (C) 2011 Elsevier B.V. All rights reserved.
Author(s)
Ji, EunkyoungMoon, HyunsooPiao, JingmeiPhuc Thi HaAn, JunyeongKim, DaeheeWoo, Jung-JeLee, YongheeMoon, Seung-HyeonRittmann, Bruce E.Chang, In Seop
Issued Date
2011-03
Type
Article
DOI
10.1016/j.bios.2010.12.039
URI
https://scholar.gist.ac.kr/handle/local/16414
Publisher
ELSEVIER ADVANCED TECHNOLOGY
Citation
Biosensors and Bioelectronics, v.26, no.7, pp.3266 - 3271
ISSN
0956-5663
Appears in Collections:
Department of Environment and Energy Engineering > 1. Journal Articles
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