• Energy Research
• 7. Clean energy close

A facultative anaerobic bacterium, designated as strain SCS5, was isolated from the anodic biofilm of a mediator-less microbial fuel cell using acetate as the electron donor and α-FeOOH as the electron acceptor. The isolate was Gram-negative, motile, and shaped as short rods (0.9-1.3 μm in length and 0.4-0.5 μm in width). A phylogenetic analysis of the 16S rRNA, gyrB, and rpoD genes suggested that strain SCS5 belonged to the Aeromonas genus in the Aeromonadaceae family and exhibited the highest 16S rRNA gene sequence similarity (99.45%) with Aeromonas jandaei ATCC 49568. However, phenotypic, cellular fatty acid profile, and DNA G+C content analyses revealed that there were some distinctions between strain SCS5 and the type strain A. jandaei ATCC 49568. The optimum growth temperature, pH, and NaCl (%) for strain SCS5 were 35°C, 7.0, and 0.5% respectively. The DNA G+C content of strain SCS5 was 59.18%. The isolate SCS5 was capable of reducing insoluble iron oxide (α-FeOOH) and transferring electrons to extracellular material (the carbon electrode). The electrochemical activity of strain SCS5 was corroborated by cyclic voltammetry and a Raman spectroscopic analysis. The cyclic voltammogram of strain SCS5 revealed two pairs of oxidation-reduction peaks under anaerobic and aerobic conditions. In contrast, no redox pair was observed for A. jandaei ATCC 49568. Thus, isolated strain SCS5 is a novel exoelectrogenic bacterium phylogenetically related to A. jandaei, but shows distinct electrochemical activity from its close relative A. jandaei ATCC 49568.

Influence of different pretreated sludge for electricity generation in microbial fuel cells (MFCs) was investigated in this study. Pre-treatment has shown significant improvement in MFC electricity productivity especially from microwave treated sludge. Higher COD reduction in the MFC has been revealed from microwave treated sludge with 55% for total and 85% for soluble COD, respectively. Nonetheless, longer ozonation treatment did not give additional advantage compared to the raw sludge. On the other hand, samples from anodes were analyzed using the 16S rRNA gene-based pyrosequencing technique for microbial community analysis. There was substantial difference in community compositions among MFCs fed with different pretreated sludge. Bacteroidetes was the abundant bacterial phylum dominated in anodes of higher productivity MFCs. These results demonstrate that using waste sludge as the substrate in MFCs could achieve both sludge reduction and electricity generation, and proper pre-treatment of sludge could improve the overall process performance.

Bench-scale decentralized wastewater treatment systems using microbial fuel cell (MFC) techniques were constructed for simultaneous removal of carbonaceous and nitrogenous pollutants and electricity production from wastewater. The MFC was operated in continuous mode and immobilized Paracoccus pantotrophus cells were added in the cathodic compartment to achieve simultaneous nitrification-denitrification. After 150-day operation, the MFC system could effectively remove >96% COD and 100% ammonium, with 60-80% total nitrogen removal and around 0.2V voltage production. The results of copper (Cu) shock load showed that although 125 mg L(-1) Cu (II) would deteriorate the effluent quality and completely inhibit the electricity production, the microbial populations restored their ability to treat wastewater and produce electricity after a period around 30 days. Community analysis by the 454 pyrosequencing technique showed that the microbial compositions were significantly different and decreased in diversity after the Cu shock load.

Carbon dioxide (CO2) is the main greenhouse gas; hence, processes are needed to remove it from the environment. Here, CO2 was used as the substrate to generate methane (CH4) by using enriched methanogens after anaerobic enrichment of waste activated sludge (WAS); therefore, we demonstrate that methanogens from WAS have significant potential for converting the greenhouse gas CO2 into the fuel methane. Methane production was found to increase 70 fold by active methanogens in the enriched methanogens culture after 3 days in the presence of H2 and CO2. Throughout the process, CO2 was completely consumed after 4 days of incubation in the vials after sparging with a mixture of H2 and CO2, resulting in significant biological CO2 sequestration by methanogens. Using a mixture of H2 and 13 CO2, we also demonstrated that the methane produced is due to the utilization of CO2. Microbial community studies via by quantitative real time PCR (qRT-PCR) indicate the dominance of archaea in the enriched methanogens culture of WAS. Archaeal community studies of the enriched methanogens via highthroughput 16S rRNA sequencing also showed that the archaea consist mainly of hydrogenotrophic and aceticlastic methanogens such as Methanobacteriaceae, Methanospirillaceae and Methanosarcinaceae spp. which are actively grown in H2 and CO2. We envision that CO2 gas from power plants can be directed to enriched methanogens of WAS to prevent release of this greenhouse gas while generating a useful biofuel (methane) or other valuable products using this single carbon atom.