Microbial fuel cells (MFCs) are a
promising technology for energy-efficient
domestic wastewater treatment, but the effluent quality has typically
not been sufficient for discharge without further treatment. A two-stage
laboratory-scale combined treatment process, consisting of microbial
fuel cells and an anaerobic fluidized bed membrane bioreactor (MFC-AFMBR),
was examined here to produce high quality effluent with minimal energy
demands. The combined system was operated continuously for 50 days
at room temperature (∼25 °C) with domestic wastewater
having a total chemical oxygen demand (tCOD) of 210 ± 11 mg/L.
At a combined hydraulic retention time (HRT) for both processes of
9 h, the effluent tCOD was reduced to 16 ± 3 mg/L (92.5% removal),
and there was nearly complete removal of total suspended solids (TSS;
from 45 ± 10 mg/L to <1 mg/L). The AFMBR was operated at a
constant high permeate flux of 16 L/m2/h over 50 days,
without the need or use of any membrane cleaning or backwashing. Total
electrical energy required for the operation of the MFC-AFMBR system
was 0.0186 kWh/m3, which was slightly less than the electrical
energy produced by the MFCs (0.0197 kWh/m3). The energy
in the methane produced in the AFMBR was comparatively negligible
(0.005 kWh/m3). These results show that a combined MFC-AFMBR
system could be used to effectively treat domestic primary effluent
at ambient temperatures, producing high effluent quality with low
energy requirements.
Scaling up microbial fuel cells (MFCs) requires the development of compact reactors with multiple electrodes. A scalable single chamber MFC (130 mL), with multiple graphite fiber brush anodes and a single air-cathode cathode chamber (27 m2/m3), was designed with a separator electrode assembly (SEA) to minimize electrode spacing. The maximum voltage produced in fed-batch operation was 0.65 V (1,000 Ω) with a textile separator, compared to only 0.18 V with a glass fiber separator due to short-circuiting by anode bristles through this separator with the cathode. The maximum power density was 975 mW/m2, with an overall chemical oxygen demand (COD) removal of>90% and a maximum coulombic efficiency (CE) of 53% (50 Ω resistor). When the reactor was switched to continuous flow operation at a hydraulic retention time (HRT) of 8 h, the cell voltage was 0.21 ± 0.04 V, with a very high CE = 85%. Voltage was reduced to 0.13 ± 0.03 V at a longer HRT = 16 h due to a lower average COD concentration, and the CE (80%) decreased slightly with increased oxygen intrusion into the reactor per amount of COD removed. Total internal resistance was 33 Ω, with a solution resistance of 2 Ω. These results show that the SEA type MFC can produce stable power and a high CE, making it useful for future continuous flow treatment using actual wastewaters.
The feasibility of a membrane contactor system for ammonia removal was studied. The mass transfer coefficient was used to quantitatively compare the effect of various operation conditions on ammonia removal efficiency. Effective removal of ammonia was possible with a Polytetrafluoroethylene (PTFE) membrane contactor system at all tested conditions. Among the various operation parameters, contact time and solution pH showed significant effect on the ammonia removal mechanism. The overall ammonia removal rate was not affected by influent suspended solution concentration unlike other pressure driven membrane filtration processes. Also the osmotic distillation phenomena which deteriorate the mass transfer efficiency can be minimized by preheating of influent wastewater. A membrane contactor system can be a possible alternative to treat high strength nitrogen wastewater by optimizing operation conditions such as stripping solution flow rate, influent wastewater temperature, and influent pH.
Treatment of domestic wastewater using microbial fuel cells (MFCs) will require reactors with multiple electrodes, but this presents unique challenges under continuous flow conditions due to large changes in the chemical oxygen demand (COD) concentration within the reactor. Domestic wastewater treatment was examined using a single-chamber MFC (130 mL) with multiple graphite fiber brush anodes wired together and a single air cathode (cathode specific area of 27 m(2)/m(3)). In fed-batch operation, where the COD concentration was spatially uniform in the reactor but changed over time, the maximum current density was 148 ± 8 mA/m(2) (1,000 Ω), the maximum power density was 120 mW/m(2), and the overall COD removal was >90 %. However, in continuous flow operation (8 h hydraulic retention time, HRT), there was a 57 % change in the COD concentration across the reactor (influent versus effluent) and the current density was only 20 ± 13 mA/m(2). Two approaches were used to increase performance under continuous flow conditions. First, the anodes were separately wired to the cathode, which increased the current density to 55 ± 15 mA/m(2). Second, two MFCs were hydraulically connected in series (each with half the original HRT) to avoid large changes in COD among the anodes in the same reactor. The second approach improved current density to 73 ± 13 mA/m(2). These results show that current generation from wastewaters in MFCs with multiple anodes, under continuous flow conditions, can be improved using multiple reactors in series, as this minimizes changes in COD in each reactor.
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