Carbon dioxide conversion to C1 - C2 compounds in a microbial electrosynthesis cell with in situ electrodeposition of nickel and iron

Abstract

This study demonstrates the continuous conversion of CO2 to methane, acetate, and ethanol in a Microbial Electrosynthesis Cell (MESC) with a carbon felt biocathode. The MESC was inoculated with a mixed anaerobic microbial consortium and operated at a mesophilic temperature of 30 °C. In situ deposition of Ni and Fe was achieved by introducing 0.2 g L−1 of NiSO4 or FeSO4, respectively, into the cathode compartment influent stream. In response, a considerable improvement in MESC performance was observed with a current density of 6.4 mA cm−2 (per separator area) and a CH4 production of 0.83 L (LR d)−1 (R = cathode volume). Once Ni and Fe were removed from the influent solution, the performance remained unchanged. Electron dispersive spectroscopy confirmed Ni and Fe electrodeposition. A shift from CH4 to acetate and ethanol production with concentrations reaching 5 and 8 g L−1, respectively, was observed upon increasing the cathode compartment pH to 8.5–9.0. 16S rRNA gene sequencing showed significant changes in the bacterial population at the cathode with Clostridia representing almost two-thirds of the population. Methanosaeta, Methanobrevibacter, and Methanobacterium species dominated the archaeal community.