Improving the Thermodynamic Energy Efficiency of Battery Electrode Deionization Using Flow-Through Electrodes
Type
ArticleAuthors
Son, MoonPothanamkandath, Vineeth
Yang, Wulin
Vrouwenvelder, Johannes S.

Gorski, Christopher A.
Logan, Bruce E.
KAUST Department
Environmental Science and Engineering ProgramWater Desalination and Reuse Research Center (WDRC)
Biological and Environmental Sciences and Engineering (BESE) Division
KAUST Grant Number
OSR-2017-CPF-2907-02Date
2020-02-24Online Publication Date
2020-02-24Print Publication Date
2020-03-17Permanent link to this record
http://hdl.handle.net/10754/661759
Metadata
Show full item recordAbstract
Ion intercalation electrodes are being investigated for use in mixed capacitive deionization (CDI) and battery electrode deionization (BDI) systems because they can achieve selective ion removal and low energy deionization. To improve the thermodynamic energy efficiency (TEE) of these systems, flow-through electrodes were developed by coating porous carbon felt electrodes with a copper hexacyanoferrate composite mixture. The TEE for ion separation using flow-through electrodes was compared to a system using flow-by electrodes with the same materials. The flow-through BDI system increased the recoverable energy nearly threefold (0.009 kWh m−3, compared to a 0.003 kWh m−3), which increased the TEE from ~6% to 8% (NaCl concentration reduction from 50 mM to 42 mM; 10 A m−2, 50% water recovery, and 0.5 mL min−1). The TEE was further increased to 12% by decreasing the flow rate from 0.50 mL min−1 to 0.25 mL min−1. These findings suggest that under similar operational conditions and materials, flow-through battery electrodes could achieve better energy recovery and TEE for desalination than flow-by electrodes.Citation
Son, M., Pothanamkandath, V., Yang, W., Vrouwenvelder, J., Gorski, C. A., & Logan, B. E. (2020). Improving the Thermodynamic Energy Efficiency of Battery Electrode Deionization Using Flow-Through Electrodes. Environmental Science & Technology. doi:10.1021/acs.est.9b06843Sponsors
This research was supported by the King Abdullah University of Science and Technology (KAUST) (OSR-2017-CPF-2907-02) and Penn State University. Support for V.P. and C.A.G. was provided by the National Science Foundation under Grant No. 1749207.Publisher
American Chemical Society (ACS)Additional Links
https://pubs.acs.org/doi/abs/10.1021/acs.est.9b06843ae974a485f413a2113503eed53cd6c53
10.1021/acs.est.9b06843