Membrane-free electrochemical deoxygenation of aqueous solutions using symmetric activated carbon electrodes in flow-through cells

Nicolas E. Holubowitch, Ayokunle Omosebi, Xin Gao, James Landon, Kunlei Liu

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

An electrochemical cell using symmetric carbon cloth electrodes and flow-through geometry that removes more than 97% of incoming aqueous dissolved oxygen (DO) is presented. The electro-deoxygenation (EDO) cell achieves O2 removal by leveraging the high overpotential of oxygen evolution on activated carbon and its propensity to oxidize under anodic polarization in aqueous solution: oxygen is reduced at the cathode while water is oxidized and incorporated into surface oxide functional groups at the anode, effectively sequestering dissolved oxygen. Polarized electrodes promote the two-step reduction of DO resulting in some residual hydrogen peroxide in the effluent, which may be beneficial for certain applications. A subsequent cell is modified with Ni cathodes downstream to reduce all H2O2 to water for particularly sensitive applications; in this cell >99% of incoming DO could be removed to lower than 10 ppb. EDO cells, which currently employ sacrificial anodes, can deaerate 30 L g−1 anode of water at an energy consumption of 1 kWh per 10,000 L; carbon anode replacement can recharge the cell. The technique is versatile, inexpensive, and environmentally friendly, deoxygenating solutions from dilute to seawater concentrations at flow rates beyond 50 ml min−1 (O2 flux = 10−4 mol s−1 m−2), more than 50x faster DO removal than similar technologies.

Original languageEnglish
Pages (from-to)163-172
Number of pages10
JournalElectrochimica Acta
Volume297
DOIs
StatePublished - Feb 20 2019

Bibliographical note

Publisher Copyright:
© 2018 Elsevier Ltd

Funding

This work was supported by the U.S.-China Clean Energy Research Center, U.S. Department of Energy [ DE-PI0000017 ], and the Carbon Management Research Group (CMRG) members: Duke Energy, Electric Power Research Institute (EPRI), Kentucky Department of Energy Development and Independence (KY-DEDI), Kentucky Power (AEP), and LG&E and KU Energy. The authors would like to thank Mr. R. Perrone for help in designing and constructing the CDI stacks.

FundersFunder number
KU Energy LLC
Kentucky Energy and Environment Cabinet Department for Energy Development
East Kentucky Power Cooperative
U.S.-China Clean Energy Research Center
U.S. Department of Energy EPSCoRDE-PI0000017
Duke Energy
Electric Power Research Institute, Louisville Gas & Electric
American Electric Power

    Keywords

    • Carbon oxidation
    • Deoxygenation
    • Flow electrochemistry
    • Oxygen reduction reaction

    ASJC Scopus subject areas

    • General Chemical Engineering
    • Electrochemistry

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