Electricity generation in microbial fuel cell systems with Thiobacillus ferrooxidans as the cathode microorganism

Microbial fuel cells (MFC) are systems that enable biochemical activities of bacteria to generate the electricity. These systems are of great interest because of their designs that enable biological activity in organic wastes to be transformed into direct electrical energy. In order to increase the commercial usage of MFCs, it is necessary to increase the power output of the system. So as to improve MFC performance, used material selection, the pH value of the used bacterial medium and the choice of the appropriate substrate are very important. In this study, oxidation bacteria Thiobacillus ferrooxidans on the cathode and mixed culture bacteria on the anode of MFC were used. Different anode and cathode pH values were examined in MFC. Best open circuit potential result (0.8 V) was obtained at anode pH 8 and cathode pH 2 conditions. In addition, three different substrates had been used in the anode. In the conditions of acetate the most stable and high valued curve was obtained. The open circuit potential had reached 0.726 V, and power density had reached 0.88 mW/cm².     

Identification of removal principles and involved bacteria in microbial fuel cells for sulfide removal and electricity generation

Simultaneous sulfide and organics removals with electricity generation can be achieved in microbial fuel cells (MFCs). In present research, principles of sulfide removal as well as the involved bacteria in the MFCs with sulfide and glucose as the complex substrate are investigated. Results indicated that electrochemical and biological oxidations are the main effects for sulfide removal. Community analysis shows a great diversity of bacteria on the anode surface, including the exoelectrogenic bacteria and sulfur-related bacteria. They are present in greater abundance than those in the MFCs fed with only sulfide and responsible for the effective electricity generation and sulfide oxidation in our proposed MFCs. The results are conducive to reveal the interactions between the pollutants and microbes in aspects of pollutants removals and energy recovery in the MFCs for sulfide removal.     

Simultaneous processes of electricity generation and ceftriaxone sodium degradation in an air-cathode single chamber microbial fuel cell

A single chamber microbial fuel cell (MFC) with an air-cathode is successfully demonstrated using glucose-ceftriaxone sodium mixtures or ceftriaxone sodium as fuel. Results show that the ceftriaxone sodium can be biodegraded and produce electricity simultaneously. Interestingly, these ceftriaxone sodium-glucose mixtures play an active role in production of electricity. The maximum power density is increased in comparison to 1000 mg L⁻¹ glucose (19 W m⁻³) by 495% for 50 mg L⁻¹ ceftriaxone sodium + 1000 mg L⁻¹ glucose (113 W m⁻³), while the maximum power density is 11 W m⁻³ using 50 mg L⁻¹ ceftriaxone sodium as the sole fuel. Moreover, ceftriaxone sodium biodegradation rate reaches 91% within 24 h using the MFC in comparison with 51% using the traditional anaerobic reactor. These results indicate that some toxic and bio-refractory organics such as antibiotic wastewater might be suitable resources for electricity generation using the MFC technology.     

Facile reconstruction of microbial fuel cell (MFC) anode with enhanced exoelectrogens selection for intensified electricity generation

The present work emphasized on the enhancement of microbial fuel cell (MFC) anode through the utilization of conductive polymer. The conductive polymer, poly(3,4-ethylenedioxythiophene) (PEDOT) was coated with varied concentrations onto graphite felt base anodes. The findings demonstrated that the optimum loading of 2.5 mg/cm² recorded maximum current density of 3.5 A/m² and coulombic efficiency of 51%. Higher loading of PEDOT enhanced the electrochemical characteristics of the anodes but exhibited unfavorable functionality. The charge transfer resistance of the modified anodes, R_a decreased significantly compared to the control anode after biofilm formation. The successful application of palm oil mill effluent (POME) wastewater as substrate indicates that the optimum anode was effective in degrading high organic wastewater. Exoelectrogens were found to be distributed mainly on the anodic biofilm. The microbial diversity of the anodes varied greatly from the inoculum and Geobacter was identified as the prevailing exoelectrogen responsible for the power generation.     

Construction and operation of a microbial fuel cell for electricity generation from wastewater

The increase in the global energy demand every year and the over-consumption of nonrenewable sources of energy has led to the identification and use of renewable and cost effective sources of energy. In this context, wastewater, which contains high levels of easily degradable organic material, has gained importance as a source of electricity generation using a microbial fuel cell.A microbial fuel cell comprising of Pseudomonas sp., mediator, and potassium ferricyanide as the oxidizing agent was developed for generation of electricity using wastewater, as substrate, obtained from wastewater treatment plant. The cells were connected in series with the anodic and cathodic solutions being introduced in batch and continuous modes. A maximum open-circuit potential of 2.2 V was obtained with the anode in batch-fed and cathode in continuous mode of operation. Methylene blue, when used as the mediator was found to produce a higher output from the cell when compared to neutral red. The maximum power output and current density obtained were 979 μW/m² and 1.15 mA/m² respectively. A 10% reduction in COD was observed when the microbial fuel cell was operated using the wastewater as the substrate.     

Production of electricity from the treatment of urban waste water using a microbial fuel cell

In this work, is studied the oxidation of the pollutants contained in an actual urban wastewater using a two-chamber microbial fuel cell (MFC). By using an anaerobic pre-treatment of the activated sludge of an urban wastewater treatment plant, the electricity generation in a MFC was obtained after a short acclimatization period of less than 10 days. The power density generated was found to depend mainly on the organic matter contain (COD) but not on the wastewater flow-rate. Maximum power densities of 25 mW m⁻² (at a cell potential of 0.23 V) were obtained. The rate of consumption of oxygen in the cathodic chamber was very low. As the oxygen reduction is coupled with the COD oxidation in the anodic chamber, the COD removed by the electricity-generating process is very small. Thus, taking into account the oxygen consumption, it was concluded that only 0.25% of the removed COD was used for the electricity-generation processes. The remaining COD should be removed by anaerobic processes. The presence of oxygen in the anodic chamber leads to a deterioration of the MFC performance. This deterioration of the MFC process occurs rapidly after the appearance of non-negligible concentrations of oxygen. Hence, to assure a good performance of this type of MFC, the growth of algae should be avoided.     

Performance improvement of air-cathode single-chamber microbial fuel cell using a mesoporous carbon modified anode

A novel mesoporous carbon (MC) modified carbon paper has been constructed using layer-by-layer self-assembly method and is used as anode in an air-cathode single-chamber microbial fuel cell (MFC) for performance improvement. Using cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS), we have demonstrated that the MC modified electrode exhibits a more favorable and stable electrochemical behavior, such as increased active surface area and enhanced electron-transfer rate, than that of the bare carbon paper. The MFC equipped with MC modified carbon paper anode achieves considerably better performance than the one equipped with bare carbon paper anode: the maximum power density is 81% higher and the startup time is 68% shorter. CV and EIS analysis confirm that the MC layer coated on the carbon paper promotes the electrochemical activity of the anodic biofilm and decreases the charge transfer resistance from 300 to 99 Ω. In addition, the anode and cathode polarization curves reveal negligible difference in cathode potentials but significant difference in anode potentials, indicating that the MC modified anode other than the cathode was responsible for the performance improvement of MFC. In this paper, we have demonstrated the utilization of MC modified carbon paper to enhance the performance of MFC.     

The effect of nitric acid,ethylenediamine, and diethanolamine modified polyaniline nanoparticles anode electrode in a microbial fuel cell

Anode materials are important in the power generation of microbial fuel cell. In this study, polyaniline was used as a conducting polymer anode in two chambers MFC. XPS and SEM were used for the characterization of functional groups of anode materials and the morphology. The power generation of microbial fuel cell was elevated by the modification of anode by nitric acid, ethylenediamine, and diethanolamine. The time that MFC reaches its maximum power generation was shortened by modification. Moreover the SEM photos prove that, it causes better attachment of microorganisms as biocatalysts on electrode surface. The best performance of among the MFCs with different anode electrodes, was the system working by polyaniline modified by ethylenediamine as that generated power of 136.2 mW/m² with a 21.3% Coulombic efficiency.     

Facile microwave-assisted synthesized reduced graphene oxide/tin oxide nanocomposite and using as anode material of microbial fuel cell to improve power generation

A new nanocomposite material was fabricated by a facile and reliable method for microbial fuel cell (MFC) anode. Tin oxide (SnO₂) nanoparticles were anchored on the surface of reduced graphene oxide (RGO/SnO₂) in two steps. The hydrothermal method was used for the modification of GO and then microwave-assisted method was used for coating of SnO₂ on the modified GO. Nanohybrids of RGO/SnO₂ achieved a maximum power density of 1624 mW m⁻², when used as the MFC anode. The obtained power density was 2.8 and 4.8 times larger than that of RGO coated and bare anodes, respectively. The electrodes were characterized by scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). The electrochemical characteristics were also studied by cyclic voltammetry (CV), linear sweep voltammetry (LSV) and electrochemical impedance spectroscopy (EIS). The high conductivity and large specific surface of the nanocomposite were greatly improved the bacterial biofilm formation and increased the electron transfer. The results demonstrate that the RGO/SnO₂ nanocomposite was advantageous material for the modification of anode and enhanced electricity generation of MFC.     

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.     

Ethane dehydrogenation over nano-Cr2O3 anode catalyst in proton ceramic fuel cell reactors to co-produce ethylene and electricity

Ethane and electrical power are co-generated in proton ceramic fuel cell reactors having Cr₂O₃ nanoparticles as anode catalyst, BaCe_0.8Y_0.15Nd_0.05O_3−δ (BCYN) perovskite oxide as proton conducting ceramic electrolyte, and Pt as cathode catalyst. Cr₂O₃ nanoparticles are synthesized by a combustion method. BaCe_0.8Y_0.15Nd_0.05O_3−δ (BCYN) perovskite oxides are obtained using a solid state reaction. The power density increases from 51 mW cm⁻² to 118 mW cm⁻² and the ethylene yield increases from about 8% to 31% when the operating temperature of the solid oxide fuel cell reactor increases from 650 °C to 750 °C. The fuel cell reactor and process are stable at 700 °C for at least 48 h. Cr₂O₃ anode catalyst exhibits much better coke resistance than Pt and Ni catalysts in ethane fuel atmosphere at 700 °C.     

Increasing power generation of microbial fuel cells with a nano-CeO2 modified anode

Nano-CeO₂ was used to modify the carbon felt anode in microbial fuel cell (MFC). The MFC with the modified anode obtained the higher closed circuit voltage resulting from the lower anode potential, the higher maximum power density (2.94 W m^?2), and the lower internal resistance (77.1 Ω). Cyclic voltammetry (CV) results implied that the bioelectrochemical activity of exoelectrogens was promoted by nano-CeO₂. Electrochemical impedance spectroscopy (EIS) results revealed that the anodic charge transfer resistance of the MFC decreased with modified anode. This study demonstrates that the nano-CeO₂ can be an effective anodic catalyst for enhancing the power generation of MFC.     

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.     

Biofilm formation and electricity generation of a microbial fuel cell started up under different external resistances

To investigate the effects of external resistance on the biofilm formation and electricity generation of microbial fuel cells (MFCs), active biomass, the content of extracellular polymeric substances (EPS) and the morphology and structure of the biofilms developed at 10, 50, 250 and 1000 Ω are characterized. It is demonstrated that the structure of biofilm plays a crucial role in the maximum power density and sustainable current generation of MFCs. The results show that the maximum power density of the MFCs increases from 0.93 ± 0.02 W m⁻² to 2.61 ± 0.18 W m⁻² when the external resistance decreases from 1000 to 50 Ω. However, on further decreasing the external resistance to 10 Ω, the maximum power density decreased to 1.25 ± 0.01 W m⁻² because of a less active biomass and higher EPS content in the biofilm. Additionally, the 10 Ω MFC shows a highest maximum sustainable current of 8.49 ± 0.19 A m⁻². This result can be attributed to the existence of void spaces beneficial for proton and buffer transport within the anode biofilm, which maintains a suitable microenvironment for electrochemically active microorganisms.     

In-situ modified titanium suboxides with polyaniline/graphene as anode to enhance biovoltage production of microbial fuel cell

Microbial fuel cell (MFC) has been the focus of much investigation in the search for harvesting electricity from various organic matters. The electrode material plays a key role in boosting MFC performance. Most studies, however, in the field of MFC electrode material has only focused on carbonaceous materials. The finding indicates that titanium suboxides (Ti₄O₇, TS) can provide a new alternative for achieving better performance. Polyaniline (PANI) together with graphene is chosen to in-situ modify TS (TSGP). The MFC reactor with TSGP anode achieves the highest voltage with 980 mV, and produces a peak power density of 2073 mW/m², which is 2.9 and 12.7 times those with the carbon cloth control. The rather intriguing result could be due to the fact that TSGP has the high conductivity and large electrochemical active surface area, greatly improving the charge transfer efficiency and the bacterial biofilm loading. This study has gone some way towards exploring the conducting ceramics materials in MFC.     

Novel carbon-ceramic composite membranes with high cation exchange properties for use in microbial fuel cell and electricity generation

Actually, there are different configurations used in microbial fuel cells (MFCs) with presence or absence of an ion exchange membrane between their electrodes. Specifically, MFCs that use membranes have the objective of avoiding the diffusion of oxygen and substrate between the anodic and cathodic compartment, and to achieve a correct transfer of protons from one chamber to another. In this regard, the current study seeks to prepare and characterize new composite membranes using as precursors three types of carbonaceous materials such as bone char, coconut shell activated carbon and bituminous activated carbon and natural clay. The composite membranes of bituminous activated carbon and clay showed more promising specific conductivity (42%) than the one made with pure clay. The physicochemical properties of the membranes and their precursors were elucidated by SEM/EDX analysis, IR spectroscopy, nitrogen adsorption isotherms at 77 K and optical microscopy. Further, membranes performance was assessed using microbial fuel cells (MFCs) where the composite membranes prepared with clay-bituminous carbon reached the highest voltage values (0.95–1.02 V) in open circuits, while that reached a maximum power density of 0.699 W/m³ at a current density of 4.012 A/m³ in closed circuit. This behavior is associated with the high content of silicon and aluminum in bituminous activated carbon, which favored the proper functioning of membranes in the MFCs. Specifically, with this type of cells, energy recovery of 0.0057 kWh/m³ and 0.1322 kWh/kg chemical oxygen demand (COD) removed, which indicates an extra economic income of the order of $0.0025/kg COD. Finally, the produced power was demonstrated in prototypes to power LED and four digital clocks. This novel clay-bituminous activated carbon showed promising cost-effectiveness and sustainable energy generation, which may be suitable for wastewater treatment.     

Electrochemical performances of solid oxide fuel cells based on Y-substituted SrTiO3 ceramic anode materials

Yttrium-substituted SrTiO₃ has been considered as anode material of solid oxide fuel cells (SOFCs) substituting of the state-of-the-art Ni cermet anodes. Sr_0.895Y_0.07TiO_3−δ (SYT) shows good electrical conductivity, compatible thermal expansion with yttria-stabilized ZrO₂ (YSZ) electrolyte and reliable stability during reduction and oxidation (redox) cycles. Single cells based on SYT anode substrates were fabricated in the dimension of 50 mm × 50 mm. The cell performances were over 1.0 A cm⁻² at 0.7 V and 800 °C, which already reached the practical application level. Although Ti diffusion from SYT substrates to YSZ electrolytes was observed, it did not show apparent disadvantage to the cell performance. The cells survived 200 redox cycles without obvious OCV decrease and macroscopic damage, but performance decreased due to the electronic properties of the SYT material. The influence of water partial pressure on cell performance and coking tolerance of the cells are also discussed in this study.     

Bismuth doped TiO2 as an excellent photocathode catalyst to enhance the performance of microbial fuel cell

Bismuth impregnation on pure TiO₂ (BiTiO₂) was carried out and tested in microbial fuel cell (MFC) as photocathode catalyst. UV–Visible spectral observation confirmed higher catalytic activity of BiTiO₂ under visible light irradiation with reduced band gap of 2.80 eV as compared to pure TiO₂ (3.26 eV). Electrochemical impedance spectroscopy also showed two times higher exchange current density with lower charge transfer resistance for BiTiO₂ (1.90 Ω) than pure TiO₂ (3.95 Ω), thus confirming it as superior oxygen reduction reaction catalyst. MFC operated with BiTiO₂ could generate a maximum power density of 224 mW m^?2, which was higher than MFC with Pt as cathode catalyst (194 mW m^?2) and much higher than MFCs with TiO₂ catalyzed cathode (68 mW m^?2) and without any cathode catalyst (60 mW m^?2). The results thus promote Bi doped TiO₂ as a superior low-cost alternative to the costly Pt catalyst to take this MFC technology forward for field application.     

Effects of mediator producer and dissolved oxygen on electricity generation in a baffled stacking microbial fuel cell treating high strength molasses wastewater

The effects of Pseudomonas aeruginosa, pyocyanin, and influent dissolved oxygen (DO) on the electricity generation in a baffled stacking microbial fuel cell (MFC) treating high strength molasses wastewater were investigated. The result shows that the influent chemical oxygen demand (COD) of 500–1000 mg l⁻¹ had the optimal substrate-energy conversion rate. The addition of a low density of P. aeruginosa (8.2 mg l⁻¹) or P. aeruginosa with pyocyanin improved the COD removal and power generation. This improvement could be attributed to the enhancement of electron transfer with the help of redox mediators. Influent DO at a concentration of up to 1.22 mg l⁻¹ did not inhibit the electricity generation. Large proportions of COD, organic-N and total-N were removed by the MFC. The MFC effluent was highly biodegradable. Denaturing gradient gel electrophoresis analysis shows that the added pyocyanin resided in the MFC for up to 14 days. An analysis of anode voltage reveals that microbial proton transport to the cathode was importantly responsible for the internal resistance.     

Performance of plug flow microbial fuel cell (PF-MFC) and complete mixing microbial fuel cell (CM-MFC) for wastewater treatment and power generation

Two flow patterns (plug flow (PF) and complete mixing (CM)) of microbial fuel cells (MFCs) with multiple anodes–cathodes were compared in continuous flow mode for wastewater treatment and power generation. The results indicated that PF-MFCs had higher power generation and columbic efficiency (CE) than CM-MFCs, and the power generation varied along with the flow pathway in the PF-MFCs. The gradient of substrate concentrations along the PF-MFCs was the driving force for the power generation. In contrast, the CM-MFCs had higher wastewater removal efficiency than PF-MFCs, but had lower power conversion efficiency and power generation. This work demonstrated that MFC configuration is a key factor for enhancing power generation and wastewater treatment.