TY - JOUR
T1 - Membrane-free electrochemical deoxygenation of aqueous solutions using symmetric activated carbon electrodes in flow-through cells
AU - Holubowitch, Nicolas E.
AU - Omosebi, Ayokunle
AU - Gao, Xin
AU - Landon, James
AU - Liu, Kunlei
N1 - Publisher Copyright:
© 2018 Elsevier Ltd
PY - 2019/2/20
Y1 - 2019/2/20
N2 - 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.
AB - 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.
KW - Carbon oxidation
KW - Deoxygenation
KW - Flow electrochemistry
KW - Oxygen reduction reaction
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U2 - 10.1016/j.electacta.2018.11.106
DO - 10.1016/j.electacta.2018.11.106
M3 - Article
AN - SCOPUS:85059317290
SN - 0013-4686
VL - 297
SP - 163
EP - 172
JO - Electrochimica Acta
JF - Electrochimica Acta
ER -