TY - JOUR
T1 - Low-Resistant Ion-Exchange Membranes for Energy Efficient Membrane Capacitive Deionization
AU - Palakkal, Varada Menon
AU - Rubio, Juan E.
AU - Lin, Yupo J.
AU - Arges, Christopher G.
N1 - Funding Information:
The work was supported by the U.S. Department of Energy (subcontracts 7F030168 and 6F-31701 from Argonne National Laboratory). We thank Dr. Bryan Pivovar and Dr. Andrew Park from the National Renewable Energy Laboratory for providing the perfluorinated AEMs. This work used the XPS and NMR tools available to the authors in the Shared Instrumentation Facility and Department of Chemistry at LSU.
Publisher Copyright:
© 2018 American Chemical Society.
PY - 2018/11/5
Y1 - 2018/11/5
N2 - Membrane capacitive deionization (MCDI) has emerged as an effective and energy efficient desalination technology for treating brackish water streams used in numerous industrial processes. Most material research studies on MCDI focus on improving the porous electrodes or using flowing electrode architectures, and little emphasis is given to the rationale design of ion-exchange membranes (IEMs) for MCDI. In this work, the ionic conductivity, permselectivity, and thickness for three different IEM chemistries (polyaliphatic, poly(arylene ether), and perfluorinated) were correlated to MCDI performance attributes: energy expended per ion removed, salt removal efficiency, and Coulombic efficiency. A 5- to 10-fold reduction in area specific resistance, which accounts for thickness and ionic conductivity, with unconventional perfluorinated and poly(arylene ether) IEMs reduced the energy expended per ion removed in MCDI by a factor of 2 when compared to conventional electrodialysis IEMs. In situ electrochemical impedance spectroscopy substantiated that thinner membranes with higher ionic conductivity helped in the reduction of energy expended per ion removed (more than 50%). Finally, the lower than 100% Coulombic efficiency is ascribed to carbon corrosion of the porous electrodes highlighting that further improvements in MCDI do not just necessitate more appropriate membranes but corrosion resilient electrodes.
AB - Membrane capacitive deionization (MCDI) has emerged as an effective and energy efficient desalination technology for treating brackish water streams used in numerous industrial processes. Most material research studies on MCDI focus on improving the porous electrodes or using flowing electrode architectures, and little emphasis is given to the rationale design of ion-exchange membranes (IEMs) for MCDI. In this work, the ionic conductivity, permselectivity, and thickness for three different IEM chemistries (polyaliphatic, poly(arylene ether), and perfluorinated) were correlated to MCDI performance attributes: energy expended per ion removed, salt removal efficiency, and Coulombic efficiency. A 5- to 10-fold reduction in area specific resistance, which accounts for thickness and ionic conductivity, with unconventional perfluorinated and poly(arylene ether) IEMs reduced the energy expended per ion removed in MCDI by a factor of 2 when compared to conventional electrodialysis IEMs. In situ electrochemical impedance spectroscopy substantiated that thinner membranes with higher ionic conductivity helped in the reduction of energy expended per ion removed (more than 50%). Finally, the lower than 100% Coulombic efficiency is ascribed to carbon corrosion of the porous electrodes highlighting that further improvements in MCDI do not just necessitate more appropriate membranes but corrosion resilient electrodes.
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U2 - 10.1021/acssuschemeng.8b01797
DO - 10.1021/acssuschemeng.8b01797
M3 - Article
AN - SCOPUS:85054312493
SN - 2168-0485
VL - 6
SP - 13778
EP - 13786
JO - ACS Sustainable Chemistry and Engineering
JF - ACS Sustainable Chemistry and Engineering
IS - 11
ER -