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Bioelectrochemical CO2 reduction is a promising method for biogas upgrading. However, the CO2 reduction efficiency in these bioelectrical systems is always relatively low and limits their applicati...

Methane (CH4)-producing bioelectrochemical systems (BES) are an attractive way to store excess renewable electricity and captured CO2. Studies have suggested that methanogenesis via direct electron uptake from a biocathode is more energetically efficient than hydrogenotrophic methanogenesis. However, mechanisms and key microorganisms involved in direct electron uptake remain unclear, primarily because of H2 produced by bacteria or extracellular hydrogenases in the system. In an attempt to minimize biological H2 production and enrich for methanogens that could efficiently convert electrons from the cathode surface to CH4, cathode chambers were pretreated with antibiotics targeting bacteria. We found that antibiotics pretreatment effectively reduced the proportion of H2-producing bacteria and H2-utilizing methanogens associated with the biocathode biofilm, and significantly promoted growth of acetoclastic methanogens from the genera Methanosarcina and Methanosaeta, several of which are known to participate ...

One pathway to remove the greenhouse gas carbon dioxide to mitigate climate change is by dissolution and electrolysis in molten carbonate to produce stable, solid carbon. This study determines critical knowledge to minimize the required electrolysis energy, the reaction stoichiometry in which carbon and O2 are the principal products, and that CO2 can be electrolyzed inexpensively. Thermochemical and experimental results indicate that the principal carbon-deposition reaction in molten Li2CO3 or Li2O/Li2CO3 electrolytes at 750 °C is Li2O + 2CO2 → Li2CO3 + C + O2. The reaction occurs at high Faradaic efficiency of the 4e– reduction of CO2 to carbon and oxygen at an electrolysis voltage as low as

Methane is the primary end product from cathodic current in microbial electrolysis cells (MECs) in the absence of methanogenic inhibitors, but little is known about the archaeal communities that develop in these systems. MECs containing cathodes made from different materials (carbon brushes, or plain graphite blocks or blocks coated with carbon black and platinum, stainless steel, nickel, ferrihydrite, magnetite, iron sulfide, or molybdenum disulfide) were inoculated with anaerobic digester sludge and acclimated at a set potential of −600 mV (versus a standard hydrogen electrode). The archaeal communities on all cathodes, except those coated with platinum, were predominated by Methanobacterium (median 97% of archaea). Cathodes with platinum contained mainly archaea most similar to Methanobrevibacter. Neither of these methanogens were abundant (

The use of thermophilic microorganisms as biocatalysts for electromethanogenesis was investigated. Single-chamber reactors inoculated with thermophiles and operated at 55 °C showed high CH4 production rates (max. 1103 mmol m(–2) day(–1) at an applied voltage of 0.8 V) with current-capture efficiencies >90%, indicating that thermophiles have high potential as biocatalysts. To improve the electromethanogenic activity, the developed biocathode was transferred to a two-chamber reactor and operated at a poised potential of −0.5 V vs SHE. The CH4 production rates of the biocathode were enhanced approximately 6-fold in 160 h of poised-potential incubation, indicating that the acclimation of the biocathode resulted in performance improvement. Compositional alteration of the cathodic microbiota suggested that a Methanothermobacter-related methanogen and synergistetes- and thermotogae-related bacteria were selected during the acclimation. Cyclic voltammetry of the “acclimated” biocathode showed an augmented cathodic catalytic wave with a midpoint potential at ca. −0.35 V vs SHE. Moreover, the biocathode was able to catalyze electromethanogenesis at −0.35 V vs SHE. These results suggested that the ability of the biocathode to catalyze electromethanogenesis via direct electron transfer was enhanced by the acclimation. This study provides new technological and fundamental information on electromethanogenic bioelectrochemical systems (BESs) that may be extended to other BESs.

The performance and biomass enrichment of the biocathode of a pair of lab-scale two-chambered microbial electrolysis cells (MEC) were assessed for 95 days as a technology for upgrading the biogas produced in anaerobic digesters, converting CO2 into CH4 through the electromethanogenic process. Two different inocula were compared: (i) a mixture of biomass from the anode of a MEC and anaerobic granular sludge (BC1); (ii) biomass enriched in a methanol-fed upflow anaerobic sludge blanket reactor (UASB) (BC2). Quantitative and qualitative microbial community assessment of the enrichment process on the biocathodes was performed by means of high-throughput sequencing of 16S rDNA- and 16S rRNA-based massive libraries as well as RT-qPCR of 16S rRNA and mcrA genes. Although BC2 had a faster increase in current density than BC1, there were no significant differences neither in the average CH4 production (0.23 ± 0.01 and 0.22 ± 0.05 L m–3 day–1 for BC1 and BC2, respectively) nor in the cathodic methane recovery efficiency (65 ± 8% and 79 ± 17%, respectively). Independently from the origin of the inoculum, total and active archaeal microbial community in both biocathodes was dominated by hydrogenotrophic methanogenic archaea, especially belonging to Methanobacteriaceae family (mainly Methanobrevibacter genus) (84–98% of both 16S rDNA and 16S rRNA relative abundance).