scholarly journals A Compact Versatile Microbial Fuel Cell From Paper

Author(s):  
Luke T. Wagner ◽  
Niloofar Hashemi ◽  
Nastaran Hashemi

Microbial fuel cells (MFCs) have been a potential green energy source for a long time but one of the problems is that either the technology must be used on a large scale or special equipment have been necessary to keep the fuel cells running such as syringe pumps. Paper-based microbial fuel cells do not need to have a syringe pump to run and can run entirely by themselves when placed in contact with the fluids that are necessary for it to run. Paper-based microbial fuel cells are also more compact than traditional MFCs since the device doesn’t need any external equipment to run. The goal of this paper is to develop a microbial fuel cell that does not require a syringe pump to function. This is done by layering chromatography paper with wax design printed onto it. This restricts the fluids to a specific flow path allowing it to act like the tubes in a typical microbial fuel cell device by delivering the fluids to the chamber. The fluids are picked up by tabs that sit in the fluid and use capillary attraction to flow up the tab and into the device. The fluids are directed to the chambers where the chemical and biological processes take place. These flows are then directed out of the device so that they are taken to a waste container and out of the system. Our microliter scale paper-based microbial fuel cell creates a significant current that is sustained for a period of time and can be repeated. A paper-based microbial fuel cell also has a fast response time. These results mean that it could be possible for a set of paper-based microbial fuel cells to create a power density capable of powering small, low power circuits when used in series or parallel. In this paper, we discuss the fabrication and experimental results of our paper-based microbial fuel cell. Also there will be a discussion of how paper-based microbial fuels cells compare to the traditional microbial fuel cells and how they could be used in the future.

2018 ◽  
Vol 7 (3.12) ◽  
pp. 69
Author(s):  
B Antony Fantin ◽  
S Ramesh ◽  
J S.Sudarsan ◽  
P Vanamoorthy Kumaran

Due to depletion of coal and other natural fuel there is an urgent need to find eco-friendly and workable technology for alternate energy. Microbial fuel cells is considered as assuringmethod to extract energy from various sources of wastewater and to generate electricity. But, due to practical limits, MFCs are still unsuitable to meet high power demands. Since wastewater contains several contaminants including organic substances, therefore, generation of electric energy from wastewater using MFC can offer an alternate solution for electricity issue as well as to reduce environmental pollution. Microbial fuel cells harvest electrical energy from wastewater with the help of microorganisms present within the wastewater. The energy confined in organic matter converted in to useful electric current. In Microbial Fuel Cell electrons from the microorganisms transfer from a reduced electron donor to an electron acceptor at a higher electrochemical potential. The study highlights that wastewater with high organic content found to be more effective and it also gives good energy production. If the same concept implemented in large scale it can help in achieving sustainable development and it helps in achieving 3R formula in the process of wastewater treatment. 


Author(s):  
A-Andrew D. Jones ◽  
Cullen R. Buie

Microbial fuel cell technology is a new technology for producing green energy from wastewater. While lab scale and commercial microbial fuel cells typically utilize graphite as the film substrate, it is difficult to rapidly prototype micro-patterned graphite and it has not been used to date. Our design sandwiches graphite sheets under a channel layer creating a microfluidic microbial fuel cell with graphite electrodes. The microfluidic microbial fuel cell uses Geobacter sulfurreducens fed with acetate in a phosphate buffer media. Ferricyanide is used as the catholyte so that the system is anodically limited. Current versus time and open circuit voltage are reported showing biofilm growth microbial fuel cell operation.


2007 ◽  
Vol 73 (16) ◽  
pp. 5347-5353 ◽  
Author(s):  
Hanno Richter ◽  
Martin Lanthier ◽  
Kelly P. Nevin ◽  
Derek R. Lovley

ABSTRACT The ability of Pelobacter carbinolicus to oxidize electron donors with electron transfer to the anodes of microbial fuel cells was evaluated because microorganisms closely related to Pelobacter species are generally abundant on the anodes of microbial fuel cells harvesting electricity from aquatic sediments. P. carbinolicus could not produce current in a microbial fuel cell with electron donors which support Fe(III) oxide reduction by this organism. Current was produced using a coculture of P. carbinolicus and Geobacter sulfurreducens with ethanol as the fuel. Ethanol consumption was associated with the transitory accumulation of acetate and hydrogen. G. sulfurreducens alone could not metabolize ethanol, suggesting that P. carbinolicus grew in the fuel cell by converting ethanol to hydrogen and acetate, which G. sulfurreducens oxidized with electron transfer to the anode. Up to 83% of the electrons available in ethanol were recovered as electricity and in the metabolic intermediate acetate. Hydrogen consumption by G. sulfurreducens was important for ethanol metabolism by P. carbinolicus. Confocal microscopy and analysis of 16S rRNA genes revealed that half of the cells growing on the anode surface were P. carbinolicus, but there was a nearly equal number of planktonic cells of P. carbinolicus. In contrast, G. sulfurreducens was primarily attached to the anode. P. carbinolicus represents the first Fe(III) oxide-reducing microorganism found to be unable to produce current in a microbial fuel cell, providing the first suggestion that the mechanisms for extracellular electron transfer to Fe(III) oxides and fuel cell anodes may be different.


Energies ◽  
2020 ◽  
Vol 13 (6) ◽  
pp. 1383 ◽  
Author(s):  
Liping Fan ◽  
Junyi Shi ◽  
Tian Gao

Proton exchange membrane is an important factor affecting the power generation capacity and water purification effect of microbial fuel cells. The performance of microbial fuel cells can be improved by modifying the proton exchange membrane by some suitable method. Microbial fuel cells with membranes modified by SiO2/PVDF (polyvinylidene difluoride), sulfonated PVDF and polymerized MMA (methyl methacrylate) electrolyte were tested and their power generation capacity and water purification effect were compared. The experimental results show that the three membrane modification methods can improve the power generation capacity and water purification effect of microbial fuel cells to some extent. Among them, the microbial fuel cell with the polymerized MMA modified membrane showed the best performance, in which the output voltage was 39.52 mV, and the electricity production current density was 18.82 mA/m2, which was 2224% higher than that of microbial fuel cell with the conventional Nafion membrane; and the COD (chemical oxygen demand) removal rate was 54.8%, which was 72.9% higher than that of microbial fuel cell with the conventional Nafion membrane. Modifying the membrane with the polymerized MMA is a very effective way to improve the performance of microbial fuel cells.


2018 ◽  
Vol 8 (12) ◽  
pp. 2384 ◽  
Author(s):  
Gene Drendel ◽  
Elizabeth R. Mathews ◽  
Lucie Semenec ◽  
Ashley E. Franks

Microbial fuel cells present an emerging technology for utilizing the metabolism of microbes to fuel processes including biofuel, energy production, and the bioremediation of environments. The application and design of microbial fuel cells are of interest to a range of disciplines including engineering, material sciences, and microbiology. In addition, these devices present numerous opportunities to improve sustainable practices in different settings, ranging from industrial to domestic. Current research is continuing to further our understanding of how the engineering, design, and microbial aspects of microbial fuel cell systems impact upon their function. As a result, researchers are continuing to expand the range of processes microbial fuel cells can be used for, as well as the efficiency of those applications.


2008 ◽  
Vol 8 (8) ◽  
pp. 4132-4134 ◽  
Author(s):  
Tushar Sharma ◽  
A. Leela Mohana Reddy ◽  
T. S. Chandra ◽  
S. Ramaprabhu

Microbial Fuel Cells (MFC) are robust devices capable of taping biological energy, converting sugars into potential sources of energy. Persistent efforts are directed towards increasing power output. However, they have not been researched to the extent of making them competitive with chemical fuel cells. The power generated in a dual-chamber MFC using neutral red (NR) as the electron mediator has been previously shown to be 152.4 mW/m2 at 412.5 mA/m2 of current density. In the present work we show that Pt thin film coated carbon paper as electrodes increase the performance of a microbial fuel cell compared to conventionally employed electrodes. The results obtained using E. coli based microbial fuel cell with methylene blue and neutral red as the electron mediator, potassium ferricyanide in the cathode compartment were systematically studied and the results obtained with Pt thin film coated over carbon paper as electrodes were compared with that of graphite electrodes. Platinum coated carbon electrodes were found to be better over the previously used for microbial fuel cells and at the same time are cheaper than the preferred pure platinum electrodes.


2016 ◽  
Vol 3 (3) ◽  
Author(s):  
T. Chailloux ◽  
A. Capitaine ◽  
B. Erable ◽  
G. Pillonnet

AbstractMicrobial fuel cells (MFC’s) are promising energy harvesters to constantly supply energy to sensors deployed in aquatic environments where solar, thermal and vibration sources are inadequate. In order to show the ready-to-use MFC potential as energy scavengers, this paper presents the association of a durable benthic MFC with a few dollars of commercially-available power management units (PMU’s) dedicated to other kinds of harvesters. With 20 cm


2016 ◽  
Vol 2 (5) ◽  
pp. 858-863 ◽  
Author(s):  
Wulin Yang ◽  
Bruce E. Logan

Microbial fuel cell (MFC) cathodes must have high performance and be resistant to water leakage.


Author(s):  
Jie Yang ◽  
Sasan Ghobadian ◽  
Reza Montazami ◽  
Nastaran Hashemi

Microbial fuel cell (MFC) technology is a promising area in the field of renewable energy because of their capability to use the energy contained in wastewater, which has been previously an untapped source of power. Microscale MFCs are desirable for their small footprints, relatively high power density, fast start-up, and environmentally-friendly process. Microbial fuel cells employ microorganisms as the biocatalysts instead of metal catalysts, which are widely applied in conventional fuel cells. MFCs are capable of generating electricity as long as nutrition is provided. Miniature MFCs have faster power generation recovery than macroscale MFCs. Additionally, since power generation density is affected by the surface-to-volume ratio, miniature MFCs can facilitate higher power density. We have designed and fabricated a microscale microbial fuel cell with a volume of 4 μL in a polydimethylsiloxane (PDMS) chamber. The anode and cathode chambers were separated by a proton exchange membrane. Carbon cloth was used for both the anode and the cathode. Shewanella Oneidensis MR-1 was chosen to be the electrogenic bacteria and was inoculated into the anode chamber. We employed Ferricyanide as the catholyte and introduced it into the cathode chamber with a constant flow rate of approximately 50 μL/hr. We used trypticase soy broth as the bacterial nutrition and added it into the anode chamber approximately every 15 hours once current dropped to base current. Using our miniature MFC, we were able to generate a maximum current of 4.62 μA.


2012 ◽  
Vol 512-515 ◽  
pp. 1525-1528 ◽  
Author(s):  
Liang Liu ◽  
Yan Yang ◽  
Ding Long Li

Cr(VI) was reduced at a carbon felt cathode in an air-cathode dual-chamber microbial fuel cell (MFC). The reduction of Cr(VI) was proven to be strongly associated with the electrogenerated H2O2 at the cathode. At pH 3.0, only 27.3% of Cr(VI) was reduced after 12h in the nitrogen-bubbling-cathode MFC, while complete reduction of Cr(VI) was achieved after 6h in the air-bubbling-cathode MFC in which the reduction of oxygen to H2O2was confirmed. The results showed that the efficient reduction of Cr(VI) could be achieved with an air-bubbling-cathode MFC.


Sign in / Sign up

Export Citation Format

Share Document