Improvement of sediment microbial fuel cell performances by design and application of power management systems

One of the ways to generate clean and non-destructive energy is to use the energy stored in the biomass resources by the microbial fuel cells (MFCs). Sediment Microbial Fuel Cells (SMFCs) are a special type of MFCs that use organic materials in aquifers sediment to generate electricity. In this research, the effects of an increase in the electrode surface are investigated. The results showed that the increase in cathode electrode surface had better efficiency than the multi-cathode mode (maximum power generated for a 3-cathode electrode (27 cm³) and 1-cathode electrode (27 cm³) was 526 mW/cm² and 800 mW/cm², respectively. Another parameter affecting the performance of these systems is temperature. In the next step, the power generation rate was measured in different step currents and at different sample times. In the final stage, a power management system (PMS) was designed to optimally utilize the output energy of the improved SMFC, leading to an increase in the output voltage to 3.3 V.     

Powering a wireless temperature sensor using sediment microbial fuel cells with vertical arrangement of electrodes

The application of wireless sensors is an important approach for monitoring natural water systems in remote locations; however, limited power sources are a key challenge for successful application of these sensors. Sediment microbial fuel cells (SMFCs) have shown potential as a sustainable power source with low maintenance requirements to power wireless sensors. This study examines electricity generation in lab-scale SMFCs with the sediment from Lake Michigan. Two SMFCs are operated in parallel with a difference in cathode arrangement (floating cathode vs. bottom cathode). The data show that the SMFC with a floating cathode produces more electricity and results in a shorter charging time when an ultracapacitor is connected to the circuit. To control electricity delivery and voltage elevation to a value that can drive a wireless temperature sensor, a power management system (PMS) is developed. With the PMS, both SMFCs can consistently power the wireless temperature sensor for data transmission to a computer, although the number of recorded data within the same period differs. This research provides an effective PMS for power control and valuable experience in SMFC configurations for the next onsite test of the developed SMFCs in Lake Michigan.     

Effect of sediment microbial fuel cell stacks on 9 V/12 V DC power supply

Sediment microbial fuel cell (SMFC) is a bio-electrochemical device that uses anaerobic bacteria to produce renewable energy. The voltage generated by SMFC is very low, so directly it cannot be applied to modern electronic devices. But, it is feasible to raise the output voltage of SMFC by connecting them in series-parallel combinations. In the present work, four SMFC modules are developed in the laboratory and by connecting in four different ways the output voltage as well as the output current are raised to the utility levels. The primary cause to avoid the practical application of series and parallel connected SMFC is voltage reversal problem. To do away with this problem, in this work each group of SMFCs is first used to charge a super-capacitor (4 F, 5.5 V) and then it has been used to power the dc boost converter. Moreover, in this research work, the effects of charging and discharging times of super capacitors for each module are also investigated. In the final stage, a dc boost converter is presented to step-up the voltage of stacked SMFCs which provides a regulated output voltage (9 V/12 V) at the load. The results obtained, show that module-4 connected boost converter provides higher output current for a longer duration as compared to other super capacitor connected modules. This technique of energy harvesting from SMFCs can be used as a power source (either of 9 V or 12 V) in practical electronic devices.     

Small boreholes embedded in the sediment layers make big difference in performance of sediment microbial fuel cells: Bioelectricity generation and microbial community

The practical applications of sediment microbial fuel cells (SMFCs) are limited by their low power densities. In this work, a novel SMFC configuration with a cylindrical borehole embedded in the sediment layer is proposed with expectations of reducing internal resistance, enhancing mass transfer, and accordingly increasing power density. Two types of boreholes with same diameter of 10 cm, but different depths of 3 cm and 6 cm are constructed in SMFCs (SMFC-3 and SMFC-6). Results demonstrate that SMFC-3 produces the highest maximum power density (65.6 mW/m²), which is 25.5% and 65.6% higher than that in SMFC-6 (52.3 mW/m²) and the control SMFC (SMFC-C, 39.4 mW/m²), respectively. The improved power performance in SMFC-3 is mainly due to the greatly reduced internal resistance. Compared to SMFC-6, the higher power density in SMFC-3 is also due to the relatively low overlying water pH values, providing suitable pH condition for cathodic reactions. Microbial community analyses demonstrate that Alphaproteobacteria and Gammaproteobacteria are major contributors to the bioelectricity, and that electroactive species enriched on the top and bottom sides of anodes are significantly different. Generally, embedding a small borehole into the sediment layer is an easy-to-implement and cost-effective strategy for improving the power performance of SMFCs.     

Using rhodium as a cathode catalyst for enhancing performance of microbial fuel cell

Rhodium with activated carbon as carbon base layer (Rh/AC) was exploited as an oxygen reduction reaction (ORR) catalyst to explore its applicability in microbial fuel cell (MFC). Four MFCs were fabricated using the Rh/AC catalyst, adopting varying Rh loadings of 0.5, 1.0 and 2.0 mg cm⁻² and without Rh on carbon felt cathode in order to understand the optimum loading of this catalyst to enhance the performance of MFC. The participation of Rh/AC in ORR was confirmed by cyclic voltammetry and electron impedance spectroscopy analysis, which supported the enhanced charge transfer capacity of the cathode modified with the prepared catalysts. Volumetric power density of MFC was found to be improved by 2.6 times when Rh/AC was used as cathode catalyst (9.36 W m⁻³) at a loading of 2.0 mg cm⁻² in comparison to the control MFC (3.65 W m⁻³) without Rh on the cathode. It was thus inferred that the increase in the Rh loading up to 2 mg cm⁻² can improve the performance of MFC significantly.     

Supercapacitors accumulating energy harvesting from stacked sediment microbial fuel cells and boosting input power for power management systems

Supercapacitors, are commonly connected to the sediment microbial fuel cell (SMFC) and then serves as the input source for the power management system (PMS). To compare and analyze functions of supercapacitors in SMFC energy harvesting, PMSs (PMS I and PMS II) are powered by SMFC stack or charged supercapacitors as the input source. Tests indicate that the charged supercapacitor results in a higher input power and a larger output power. In addition, the overall efficiency of PMSs is rarely affected by the capacitance, but the initial voltage of the supercapacitor. By charging supercapacitors connected in parallel and then discharging them in series, the overall power efficiency of PMS II is increased from 44.33% to 69.52%. In conclusion, supercapacitors firstly storing SMFC energy is beneficial to provide sufficient energy, resulting in an improved PMS performance. Further, these results can be useful and informative to PMS design for efficiently harvesting and utilize MFC energy.     

Innovative microbial fuel cell for electricity production from anaerobic reactors

A submersible microbial fuel cell (SMFC) was developed by immersing an anode electrode and a cathode chamber in an anaerobic reactor. Domestic wastewater was used as the medium and the inoculum in the experiments. The SMFC could successfully generate a stable voltage of 0.428 ± 0.003 V with a fixed 470 Ω resistor from acetate. From the polarization test, the maximum power density of 204 mW m⁻² was obtained at current density of 595 mA m⁻² (external resistance = 180 Ω). The power generation showed a saturation-type relationship as a function of wastewater strength, with a maximum power density (P_max) of 218 mW m⁻² and a saturation constant (K_s) of 244 mg L⁻¹. The main limitations for achieving higher electricity production in the SMFC were identified as the high internal resistance at the electrolyte and the inefficient electron transfer at the cathode electrode. As the current increased, a large portion of voltage drop was caused by the ohmic (electrolyte) resistance of the medium present between two electrodes, although the two electrodes were closely positioned (about 3 cm distance; internal resistance = 35 ± 2 Ω). The open circuit potential (0.393 V vs. a standard hydrogen electrode) of the cathode was much smaller than the theoretical value (0.804 V). Besides, the short circuit potential of the cathode electrode decreased during the power generation in the SMFC. These results demonstrate that the SMFC could successfully generate electricity from wastewater, and has a great potential for electricity production from existing anaerobic reactors or other anaerobic environments such as sediments. The advantage of the SMFC is that no special anaerobic chamber (anode chamber) is needed, as existing anaerobic reactors can be used, where the cathode chamber and anode electrode are immersed.     

Electricity generation with a sediment microbial fuel cell equipped with an air-cathode system using photobacterium

The main purpose of this study is the characteristic and nature of current generation with a pure culture of single cell in a sediment microbial fuel cell. A sediment microbial fuel cell with an air-cathode system was studied for a prolonged period of time. The current maintained a steady increase throughout the entire time period and reached to its peak of 1.82 μA with power density of 29,024.65 μW/cm² at day 35. Water parameters such as salinity and pH were observed throughout the entire time period for better understanding. Operation of water parameter had been done after stabilization of current output for every measurement. The electron transfer pathway was assessed by cyclic voltammetry study. A low current density was observed due to profound internal resistance (141 Ω), and the reason for which was ohmic losses. A linear relationship was observed between current density and power density. Phylogenetic analysis was performed with 16S rRNA to identify the studied organism.     

Design of thermal management subsystem for a 5 kW polymer electrolyte membrane fuel cell system

High-efficiency thermal management subsystem has a key role on the PEM fuel cell performance and durability. In this study, design of thermal management subsystem for a 5 kW PEM fuel cell system is investigated. A numerical model is presented to study the cooling flow field performance. The number of parallel channels in parallel serpentine flow field is selected as the design parameter of the flow field and its optimum value is obtained by compromising between the minimum pressure drop of coolant across the flow field and maximum temperature uniformity within the bipolar plate criteria. The optimum coolant flow rate is also determined by compromising between different criteria. Test results of a 5-cells short stack are presented to verify the numerical simulation results.     

Power generation from furfural using the microbial fuel cell

Furfural is a typical inhibitor in the ethanol fermentation process using lignocellulosic hydrolysates as raw materials. In the literature, no report has shown that furfural can be utilized as the fuel to produce electricity in the microbial fuel cell (MFC), a device that uses microbes to convert organic compounds to generate electricity. In this study, we demonstrated that electricity was successfully generated using furfural as the sole fuel in both the ferricyanide-cathode MFC and the air-cathode MFC. In the ferricyanide-cathode MFC, the maximum power densities reached 45.4, 81.4, and 103 W m⁻³, respectively, when 1000 mg L⁻¹ glucose, a mixture of 200 mg L⁻¹ glucose and 5 mM furfural, and 6.68 mM furfural were used as the fuels in the anode solution. The corresponding Coulombic efficiencies (CE) were 4.0, 7.1, and 10.2% for the three treatments, respectively. For pure furfural as the fuel, the removal efficiency of furfural reached up to 95% within 12 h. In the air-cathode MFC using 6.68 mM furfural as the fuel, the maximum values of power density and CE were 361 mW m⁻² (18 W m⁻³) and 30.3%, respectively, and the COD removal was about 68% at the end of the experiment (about 30 h). Increase in furfural concentrations from 6.68 to 20 mM resulted in increase in the maximum power densities from 361 to 368 mW m⁻², and decrease in CEs from 30.3 to 20.6%. These results indicated that some toxic and biorefractory organics such as furfural might still be suitable resources for electricity generation using the MFC technology.     

Simultaneous degradation of P-nitroaniline and electricity generation by using a microfiltration membrane dual-chamber microbial fuel cell

Microfiltration membrane, a potential alternative for traditional proton exchange membrane (PEM) due to its strong ability of proton transfer, cost-effectiveness, sustainability and high anti-pollution capability in microbial fuel cell (MFC). In this study, a novel MFC using bilayer microfiltration membrane as separator, inoculated sludge as biocatalyst and P-nitroaniline (PNA) as electron donor was successfully constructed to evaluate its performance. Furthermore, we also investigated the effects of initial PNA concentration, co-substrate (acetate) and cultivated microorganisms on MFC performance. Results showed that the maximum power density of 4.43, 3.05, 2.62 and 2.18 mW m^?2 was acquired with 50, 100, 150 and 300 mg L^?1 of PNA as substrate, respectively. However, with the addition of 500 mg L^?1 of acetate into reaction system contained 100 mg L^?1 of PNA, the higher power production of 6.24 mW m^?2 was obtained, which was 2.05 times higher than that using 100 mg L^?1 of PNA as the sole substrate. Meanwhile, the MFC working on cultivated microorganisms displayed a maximal power density of 7.32 mW m^?2 and a maximum PNA degradation efficiency of 54.75%. And after an electricity production cycle, the number of microbes in the anode chamber significantly increased. This study provides a promising technology for bioelectricity generation by biodegrading biorefractory pollutants in wastewater.     

Evaluating the performance of microbial fuel cells powering electronic devices

A microbial fuel cell (MFC) is capable of powering an electronic device if we store the energy in an external storage device, such as a capacitor, and dispense that energy intermittently in bursts of high-power when needed. Therefore its performance needs to be evaluated using an energy-storing device such as a capacitor which can be charged and discharged rather than other evaluation techniques, such as continuous energy dissipation through a resistor. In this study, we develop a method of testing microbial fuel cell performance based on storing energy in a capacitor. When a capacitor is connected to a MFC it acts like a variable resistor and stores energy from the MFC at a variable rate. In practice the application of this method to testing microbial fuel cells is very challenging and time consuming; therefore we have custom-designed a microbial fuel cell tester (MFCT). The MFCT evaluates the performance of a MFC as a power source. It uses a capacitor as an energy storing device and waits until a desired amount of energy is stored then discharges the capacitor. The entire process is controlled using an analog-to-digital converter (ADC) board controlled by a custom-written computer program. The utility of our method and the MFCT is demonstrated using a laboratory microbial fuel cell (LMFC) and a sediment microbial fuel cell (SMFC). We determine (1) how frequently a MFC can charge a capacitor, (2) which electrode is current-limiting, (3) what capacitor value will allow the maximum harvested energy from a MFC, which is called the “optimum charging capacitor value,” and (4) what capacitor charging potential will harvest the maximum energy from a MFC, which is called the “optimum charging potential.” Using a LMFC we find that (1) the time needed to charge a 3-F capacitor from 0 to 500 mV is 108 min, (2) the optimum charging capacitor value is 3 F, and (3) the optimum charging potential is 300 mV. Using a SMFC we find that (1) the time needed to charge a 3-F capacitor from 0 to 500 mV is 5 min, (2) the optimum charging capacitor value is 3 F, and (3) the optimum charging potential is 500 mV. Our results demonstrate that the developed method and the MFCT can be used to evaluate and optimize energy harvesting when a MFC is used with a capacitor to power wireless sensors monitoring the environment.     

Effects of initial sediment properties on start-up times for sediment microbial fuel cells

Sediment microbial fuel cells (SMFCs) are being developed as a renewable power source to aid environmental remediation and provide remote monitoring. But long start-up times limit their use as a viable industrial approach. In this study, we sampled sediments from seven different levels of eutrophication lakes and investigated the effects of their initial sediment properties (ISP) on the start-up times of SMFCs. After 60 days, ISP showed a clear influence on SMFCs with start-up times ranging from 7 to 21 days at different sampling sites. Organic matter, especially the labile carbon pools and nitrogen (organic and inorganic) contents in sediment, were closely related to start-up times for the SMFCs. In addition, dehydrogenase activity and high-throughput sequencing revealed that microorganisms in the nutrient enrichment sediments increased organic matter degradation and produced special species such as genus Candidatus Xiphinematobacter that belong to the Verrucomicrobia phyla related to electron transfer. Such active control may improve applicability by accelerating start-up and enhancing SMFC power and bio-catalytic performance.     

New design of benthic microbial fuel cell for bioelectricity generation: Comparative study

Benthic microbial fuel cells (BMFCs) are the potential sources for energy generation in which the chemical energy stored in the bonds between organic and non-organic materials are turned into electricity using microorganisms as the catalysts. In this study, new anodic chamber is fabricated for BMFC. The environmental conditions similar to those of Caspian Sea water have been applied to an experimental setup. The output power density in the BMFC has been measured and evaluated using various electrodes including graphite plate (GP), carbon cloth (CC) and granular activated carbon (GAC) at various distances 10, 20 and 50 cm, in different current and time steps. Based on the obtained results, too close or too far distance between the electrodes leads to an increase in the internal resistance and reduces the performance of the cell. In this regard, the optimized distance for the electrodes has been found to be 20 cm. The maximum power density of the GAC electrode before using the anodic chamber was 92.85 mW/m² in current density of 324.67 mA/m². This value has reached 170.02 mW/m² and 422.02 mA/m² after deployment in the anodic chamber under the same environmental conditions, which indicates that the maximum power density experienced an approximately double increase compared to the previous state.     

Adaptive real-time optimal energy management strategy based on equivalent factors optimization for hybrid fuel cell system

Fuel cell, a new kind of energy supply equipment, has several advantages such as high efficiency, low noise, and no emission. Proton exchange membrane fuel cell (PEMFC) is considered to have the potential to take the place of the conventional engine on unmanned underwater vehicle (UUV). Besides the power sources in the hybrid power system, the energy management system (EMS) is crucial to operating performance. In this paper, an on-line adaptive equivalent hydrogen consumption minimization strategy (ECMS) is proposed to solve the problem of prior knowledge demand and poor adaptability of current energy management algorithms. In this presented method, a battery state of charge (SOC) constituted penalty term is designed to calculate the equivalent factor (EF), and then the equivalent factor obtained by optimization is substituted into the original objective equation to realize the real-time energy regulation. In this paper, a typical UUV load curve is used to verify the control effect under different working conditions, and the performance is compared with three conventional algorithms’. Simulation results show that the hydrogen consumption of proposed algorithm is close to the optimal solution obtained in offline environment, and it is reduced by more than 3.79% compared with the traditional online methods.     

Co-substrate strategy for improved power production and chlorophenol degradation in a microbial fuel cell

A co-substrate strategy has the potential to contribute toward minimizing the poisoning of refractories on the anode respiring bacteria (ARB), which is a necessity for microbial fuel cell (MFC) to recover energy from toxic wastewater. However, little is known about the underlying mechanisms. This study employed 4-chlorophenol (4-CP) as target refractory pollutant and acetate as co-substrate. The co-substrate could stimulate 4-CP sensitive extracellular electron transfer (EET) enzymes’ activity under 4-CP stress, such as succinate dehydrogenase (complex II) and cytochromes c OmcA and OmcB. For the microbial community, ARB were still abundant during 4-CP toxification; Azospirillum and Dechloromonas were enriched to conduct aromatic ring breakage and dechlorination. Thus, a 4.3-fold increased power generation was achieved, and the 4-CP and chemical oxygen demand (COD) removals increased by ∼42% and ∼53%, respectively. An easy-to-degrade substrate could improve power re-coverage from refractory wastewater by enhancing EET enzyme activity and optimizing the microbial community.     

Acclimatization of a microbial consortium into a stable biofilm to produce energy and 1,3-propanediol from glycerol in a microbial fuel cell

Glycerol, a by-product of biodiesel production, is a potential substrate for producing electricity and value-added products in bioelectrochemical systems. Here, we demonstrate a strategy to establish a highly specific energy-producing biofilm from glycerol in a microbial fuel cell (MFC). The MFC fed with 1 g L^?1 glycerol achieved maximum voltage, power density, and current of 0.4 V, 152 mW m^?2, and 19.0 mA m^?2, respectively, operating at a resistance of 1000 Ω. These values were much higher than the values previously described for the same glycerol concentration. High-throughput sequencing demonstrated that substituting acetate for glycerol diminished the anodic microbial diversity. In addition, glycerol shifted the microbial community composition from electroactive bacteria genera such as Delftia, Advenella, Thauera, Stenotrophomonas, and Dysgonomonas to bacteria with dual functions of electricity generation and 1,3-propanediol formation, including Citrobacter, Pseudomonas, and Klebsiella. Thus, establishing this biofilm opens the possibility of recovering energy and obtaining an added-value product from glycerol.     

Automatic control of load increases power and efficiency in a microbial fuel cell

Increasing power production and coulombic efficiency (CE) of microbial fuel cells (MFCs) is a common research ambition as the viability of the technology depends to some extent on these measures of performance. As MFCs are typically time varying systems, comparative studies of controlled and un-controlled external load impedance are needed to show if control affects the biocatalyst development and hence MFC performance. The application of logic based control of external load resistance is shown to increase the power generated by the MFC, when compared to an equivalent system which has a static resistive load. The controlled MFC generated 1600 ± 400 C, compared to 300 ± 10 C with an otherwise replicate fixed load MFC system. The use of a parsimonious gradient based control was able to increase the CE to within the range of 15.1-22.7%, while the CE for a 200 Ω statically loaded MFC lay in the range 3.3-3.7%. The controlled MFC improves the electrogenic anodic biofilm selection for power production, indicating that greater power and substrate conversion can be achieved by controlling load impedance. Load control ensured sustainable current demand, applied microbial selection pressures and provided near-optimal impedance for power transference, compared to the un-controlled system.     

Manipulating the hydrogen production from acetate in a microbial electrolysis cell-microbial fuel cell-coupled system

A biological hydrogen-producing system is configured through coupling an electricity-assisting microbial fuel cell (MFC) with a hydrogen-producing microbial electrolysis cell (MEC). The advantage of this biocatalyzed system is the in-situ utilization of the electric energy generated by an MFC for hydrogen production in an MEC without external power supply. In this study, it is demonstrated that the hydrogen production in such an MEC-MFC-coupled system can be manipulated through adjusting the power input on the MEC. The power input of the MEC is regulated by applying different loading resistors connected into the circuit in series. When the loading resistance changes from 10 Ω to 10 kΩ, the circuit current and volumetric hydrogen production rate varies in a range of 78 ± 12 to 9 ± 0 mA m⁻² and 2.9 ± 0.2 to 0.2 ± 0.0 mL L⁻¹ d⁻¹, respectively. The hydrogen recovery (RH₂), Coulombic efficiency (CE), and hydrogen yield (YH₂) decrease with the increase in loading resistance. Thereafter, in order to add power supply for hydrogen production in the MEC, additional one or two MFCs are introduced into this coupled system. When the MFCs are connected in series, the hydrogen production is significantly enhanced. In comparison, the parallel connection slightly reduces the hydrogen production. Connecting several MFCs in series is able to effectively increase power supply for hydrogen production, and has a potential to be used as a strategy to enhance hydrogen production in the MEC-MFC-coupled system from wastes.     

Regenerative energy control system for plug-in hydrogen fuel cell scooter

An intelligent control system was developed using simple control methodologies for an H₂-powered fuel cell scooter with the aid of a built-in microprocessor. This system increases the power input to drive a hydrogen fuel cell scooter, particularly during uphill conditions by running both the batteries and the fuel cell source in parallel. This system also improves the energy management of the scooter by recharging the battery using the fuel cell as well as automatic switching to the battery source when the hydrogen fuel cell is running low on hydrogen. This system was tested on a bench set simulating a 254 W hydrogen fuel cell stack equipped on a 200 W scooter. The test rig set-up depicts a practical scooter running on various load conditions. These results reflect the efficiencies of actual running conditions. The entire operation was embedded in a PICAXE-18 microcontroller for automatic switching between the batteries and the fuel cell source. An increase in the DC motor efficiency by 6 % has been shown. The uphill angle of the scooter has been increased by 19.3 %, which means the scooter would be able to travel on steeper hills. Copyright © 2007 John Wiley & Sons, Ltd.