The reduction of CO2/bicarbonate to ethanol driven by Bio-electrochemical system using reduced graphene oxide modified nickel foam
[Display omitted] •Driven by bio-electricity in MFC, CO2/ bicarbonate were reduced in cathode.•The RGO-Ni material exhibited excellent performance in the process of CO2/ bicarbonate reduction.•After reaction for 6 h, the ethanol produced in catholyte was tested at 167 mg L-1. In this study, the redu...
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Veröffentlicht in: | Separation and purification technology 2022-01, Vol.280, p.119437, Article 119437 |
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Sprache: | eng |
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•Driven by bio-electricity in MFC, CO2/ bicarbonate were reduced in cathode.•The RGO-Ni material exhibited excellent performance in the process of CO2/ bicarbonate reduction.•After reaction for 6 h, the ethanol produced in catholyte was tested at 167 mg L-1.
In this study, the reduced graphene oxide modified nickel foam (abbreviated as RGO-Ni) was used as catalytic cathode to reduce CO2/bicarbonate to produce organics in catholyte (containing 0.45 M KHCO3), driven by bio-electrochemical system. The characterization of electrode materials were tested by Scanning Electron Microscope (SEM) and Cyclic Voltammetry curves (CV). The reduction products was analyzed by Gas Chromatograph - Mass Spectrometer (GC–MS). The power generation and the faradic efficiency of the reduction process was determined. The results indicated the RGO-Ni electrode showed much higher catalytic activity than Ni electrode or graphene oxide modified Ni electrode (GO-Ni). The results of GC–MS indicated the reduction products were ethanol (as primary product) and acetone (as by product). Over the RGO-Ni cathode, after 6 h reaction in catholyte with CO2 continuously aerated, the final concentration of Chemical Oxygen Demand (COD) was 389 mg L-1, and the concentration of ethanol was 167 mg L-1. The process maximum power density was 0.52 W m−2 over RGO-Ni electrode, almost 17 times of the value (0.03 W m−2) using Ni cathode. The faradaic efficiency of the process was calculated as 70%, and the reduction mechanism of CO2/bicarbonate was suggested. |
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ISSN: | 1383-5866 1873-3794 |
DOI: | 10.1016/j.seppur.2021.119437 |