scholarly journals Preparation of nickel manganese oxide modified ni foam for anode catalyst direct urea fuel cell

2020 ◽  
Vol 211 ◽  
pp. 03004
Author(s):  
Yola Yolanda ◽  
Muhammad Ridwan ◽  
Jong Wook Hong ◽  
Tribidasari Anggarainum Ivandini

Renewable energy is known as environmentally friendly, such as fuel cells. Nickel is regarded as one of the most promising transition metals to be applied as an electrocatalyst in fuel cell application due to its high catalytic activity. However, the modification of nickel is required to decrease its overpotential. In the present study, the NiMn2O4/Ni-foam was prepared for an anode catalyst in the direct urea fuel cell. The NiMn2O4/Nifoam was synthesized through the hydrothermal method at 180°C for 24 h using Mn(NO3)2.6H2O and Ni(NO3)2.6H2O solutions as the precursors in the presence of urea. During the reaction, Ni foam was placed in the solution to undergo the reaction inside the porous of the Ni-foam. Cyclic voltammetry of the prepared NiMn2O4/Ni-foam electrode in a 2 M KOH solution and 0.33 M urea showed good maximum current density at 206 mA cm-2. Furthermore, the prepared electrode was examined in a direct urea fuel cell with a solution containing 2 M KOH and 0.33 M urea in the anode chamber and a solution containing 2 M H2O2 and 2 M H2SO4 in the anode chamber. A power density of 0.304 mW cm-2 was achieved, indicating the prepared electrode is promising to be developed for a catalyst in a direct urea fuel cell.

2015 ◽  
Vol 5 (1) ◽  
Author(s):  
Carlo Santoro ◽  
Alexey Serov ◽  
Claudia W. Narvaez Villarrubia ◽  
Sarah Stariha ◽  
Sofia Babanova ◽  
...  

2018 ◽  
Vol 15 (4) ◽  
pp. 981-986 ◽  
Author(s):  
Mohamed E. Osman ◽  
Om-Kolthoum H. Khattab ◽  
Abo Elnasr A.A. ◽  
Abdel Basset S.

A microbial fuel cell (MFC) has great potential for azo dyes decolorization and electricity generation by using filamentous fungi as biocatalysts. In this study, Aspergillus niger and Trichoderma harzianum were inoculated in anode chamber of double-chamber MFC to decolorize azo dye acid black 172 with Potassium Ferricyanide in the cathode chamber. During MFC operations, Acid black 172 oxidized and produced a maximum open-circuit voltage of 890 mV, and maximum current density of 163 mA/m2 with an external resistance of 1000Ω. Also, variable parameters such as dye concentration, Co-substrate and dye as a sole carbon source were studied to improve microbial fuel cell performance.


Energies ◽  
2019 ◽  
Vol 12 (18) ◽  
pp. 3532 ◽  
Author(s):  
Miguel Ángel López Zavala ◽  
Omar Israel González Peña ◽  
Héctor Cabral Ruelas ◽  
Cristina Delgado Mena ◽  
Mokhtar Guizani

Cyclic voltammetry (CV) was used in this work to describe the electrochemical behavior of a dual-chamber microbial fuel cell (MFC). The system performance was evaluated under vacuum and non-pressurized conditions, different reaction times, two sweep potentials, 25 and 50 mVs−1 and under different analyte solutions, such as distilled water and domestic wastewater. CV experiments were conducted by using a potentiostat with three different configurations to collect the measurements. A dual-chamber MFC system was equipped with a DupontTM Nafion® 117 proton exchange membrane (PEM), graphite electrodes (8.0 cm × 2.5 cm × 0.2 cm) and an external electric circuit with a 100-Ω resistor. An electrolyte (0.1 M HCl, pH ≈ 1.8) was used in the cathode chamber. It was found that the proton exchange membrane plays a major role on the electrochemical behavior of the MFC when CV measurements allow observing the conductivity performance in the MFC in the absence of a reference electrode; under this potentiostat setting, less current density values are obtained on the scanned window potentials. Therefore, potentiostat setting is essential to obtain information in complex electrochemical processes present in biological systems, such as it is the case in the MFCs. Results of the study showed that wastewater constituents and the biomass suspended or attached (biofilm) over the electrode limited the electron charge transfer through the interface electrode-biofilm-liquor. This limitation can be overcome by: (i) Enhancing the conductivity of the liquor, which is a reduction of the ohmic drop, (ii) reducing the activation losses by a better catalysis, and (iii) by limiting the diffusional gradients in the bulk liquor, for instance, by forced convection. The use of the electrolyte (0.1 M HCl, pH ≈ 1.8) and its diffusion from the cathode to the anode chamber reduces the resistance to the flow of ions through the PEM and the flow of electrons through the anodic and cathodic electrolytes. Also reduces the activation losses during the electron transfer from the substrate to the electrode surface due to the electrode catalysis improvement. On the other hand, vacuum also demonstrated that it enhances the electrochemical performance of the dual-chamber MFC due to the fact that higher current densities in the system are favored.


2008 ◽  
Vol 58 (1) ◽  
pp. 37-43 ◽  
Author(s):  
M. M. Ghangrekar ◽  
V. B. Shinde

Long term performance of mediator-less and membrane-less microbial fuel cell (ML-MFC) was evaluated for treatment of synthetic and actual sewage and electricity harvesting. The anode chamber of ML-MFC was inoculated with pre-heated mixed anaerobic sludge collected from a septic tank. The ML-MFC was operated by feeding synthetic wastewater for first 244 days, under different organic loading rates, and later with actual sewage for next 30 days. Maximum chemical oxygen demand (COD) removal efficiency of 91.4% and 82.7% was achieved while treating synthetic wastewater and actual sewage, respectively. Maximum current of 0.33 mA and 0.17 mA was produced during synthetic and actual sewage treatment, respectively. Maximum power density of 6.73 mW/m2 (13.65 mW/m3) and maximum current density of 70.74 mA/m2 was obtained in this membrane-less MFC with successful organic matter removal from wastewater.


2006 ◽  
Vol 278 (1-2) ◽  
pp. 35-42 ◽  
Author(s):  
Philippe Bébin ◽  
Magaly Caravanier ◽  
Hervé Galiano

2007 ◽  
Vol 88 (1) ◽  
pp. 3-22 ◽  
Author(s):  
Aidu Qi ◽  
Brant Peppley ◽  
Kunal Karan

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