ABSTRACT
Human activities release more carbon dioxide (CO2) into the atmosphere than the natural process can remove. This study attempts to address the main challenges for the thermophilic (50 °C) bioelectrochemical conversion of CO2 into acetate. First, real gaseous emissions were tested with mixed microbial consortia, which had no substantial influence on production rates (difference of 2.5%). Subsequently, a bench-scale system (TRL 4-5) was designed and launched to control key operational variables. Fixing the current at 1.3 A m-2, CO2 was reduced at a rate of 2.21 kg CO2 kg-1 acetate, while the electricity consumption was 2.07 kWh kg-1, the most efficient value so far. The results suggest that the operation with real effluents is feasible and the proposed design is energy efficient, but the right balance between maximising current densities without compromising the biocompatibility with catalysts will determine the transition from laboratory scale towards its implementation in the market.
Subject(s)
Carbon Dioxide , Gases , Humans , Electricity , Acetates , Vehicle EmissionsABSTRACT
The feasibility of using microbial fuel cells (MFCs) in landfill leachate treatment and electricity production was assessed under high levels of nitrogen concentration (6033 mg NL(-1)) and conductivity (73,588 µS cm(-1)). An air-cathode MFC was used over a period of 155 days to treat urban landfill leachate. Up to 8.5 kg COD m(-3)d(-1) of biodegradable organic matter was removed at the same time as electricity (344 m Wm(-3)) was produced. Nitrogen compounds suffered transformations in the MFC. Ammonium was oxidized to nitrite using oxygen diffused from the membrane. However, at high free ammonia concentrations (around 900 mg N-NH(3)L(-1)), the activity of nitrifier microorganisms was inhibited. Ammonium reduction was also resulted from ammonium transfer through the membrane or from ammonia loss. High salinity content benefited the MFC performance increasing power production and decreasing the internal resistance.
