• Energy Research

Microbial anodes were formed under polarization at -0.3 V/SCE on graphite plates in effluents from a pulp and paper mill. The bioanodes formed with the addition of acetate led to the highest current densities (up to 6A/m(2)) but were then unable to oxidize the raw effluent efficiently (0.5A/m(2)). In contrast, the bioanodes formed without acetate addition were fully able to oxidize the organic matter contained in the effluent, giving up to 4.5A/m(2) in continuous mode. Bacterial communities showed less bacterial diversity for the acetate-fed bioanodes compared to those formed in raw effluents. Deltaproteobacteria were the most abundant taxonomic group, with a high diversity for bioanodes formed without acetate addition but with almost 100% Desulfuromonas for the acetate-fed bioanodes. The addition of acetate to form the microbial anodes induced microbial selection, which was detrimental to the treatment of the raw effluent.

Microbial anodes were formed under polarization at -0.3 V/SCE on graphite plates in effluents from a pulp and paper mill. The bioanodes formed with the addition of acetate led to the highest current densities (up to 6A/m(2)) but were then unable to oxidize the raw effluent efficiently (0.5A/m(2)). In contrast, the bioanodes formed without acetate addition were fully able to oxidize the organic matter contained in the effluent, giving up to 4.5A/m(2) in continuous mode. Bacterial communities showed less bacterial diversity for the acetate-fed bioanodes compared to those formed in raw effluents. Deltaproteobacteria were the most abundant taxonomic group, with a high diversity for bioanodes formed without acetate addition but with almost 100% Desulfuromonas for the acetate-fed bioanodes. The addition of acetate to form the microbial anodes induced microbial selection, which was detrimental to the treatment of the raw effluent.

Six biocathodes catalyzing oxygen reduction were designed from the same environmental inoculum but using three different methods. Two were formed freely at open circuit potential, two using conventional aerobic polarization at -0.2V/SCE and two by reversion of already established acetate-fed bioanodes. Observation of the biofilms by SEM and epifluorescence microscopy revealed that reversible bioelectrodes had the densest biofilms. Electrochemical characterization revealed two different redox systems for oxygen reduction, at -0.30 and +0.23V/SCE. The biocathodes formed under aerobic polarization gave higher electrocalatytic performance for O2 reduction, due to production of the redox systems at +0.23V/SCE. Analyses of the bacterial communities on the biocathodes by 16S-rRNA pyrosequencing showed different selection (or enrichment) of microorganisms depending on the method used. This study highlights how the method chosen for designing oxygen biocathodes can affect the cathode coverage, the selection of bacterial populations and the electrochemical performance.

Six biocathodes catalyzing oxygen reduction were designed from the same environmental inoculum but using three different methods. Two were formed freely at open circuit potential, two using conventional aerobic polarization at -0.2V/SCE and two by reversion of already established acetate-fed bioanodes. Observation of the biofilms by SEM and epifluorescence microscopy revealed that reversible bioelectrodes had the densest biofilms. Electrochemical characterization revealed two different redox systems for oxygen reduction, at -0.30 and +0.23V/SCE. The biocathodes formed under aerobic polarization gave higher electrocalatytic performance for O2 reduction, due to production of the redox systems at +0.23V/SCE. Analyses of the bacterial communities on the biocathodes by 16S-rRNA pyrosequencing showed different selection (or enrichment) of microorganisms depending on the method used. This study highlights how the method chosen for designing oxygen biocathodes can affect the cathode coverage, the selection of bacterial populations and the electrochemical performance.