Comparing specific capacitance in rice husk-derived activated carbon through phosphoric acid and potassium hydroxide activation order variations.

This manuscript investigates the influence of the chemical activation step order and process parameters on the specific capacitance of activated carbon derived from rice husk. The chemical activation was performed either before or after the carbonization step, using phosphoric acid (H3PO4) and potassium hydroxide (KOH) as activating agents. For activation before carbonization, the carbonization process was conducted at various temperatures (600, 750, 850, and 1050 °C). On the other hand, for activation after carbonization, the effect of the volume of the chemical agent solution was studied, with 0, 6, 18, 21, 24, and 30 mL/g of phosphoric acid and 0, 18, 30, 45, 60, and 90 mL/g of 3.0 M KOH solution. The results revealed that in the case of chemical activation before carbonization, the optimum temperature for maximizing specific capacitance was determined to be 900 °C. Conversely, in the case of chemical activation after carbonization, the optimal volumes of the chemical agent solutions were found to be 30 mL/g for phosphoric acid (H3PO4) and 21 mL/g for potassium hydroxide (KOH). Moreover, it was observed that utilizing phosphoric acid treatment before the carbonization step leads to an 21% increase in specific capacitance, attributed to the retention of inorganic compounds, particularly silica (SiO2). Conversely, when rice husks were treated with KOH after the carbonization step, the specific capacitance was found to be doubled compared to treatment with KOH prior to the carbonization step due to embedding of SiO2 and KHCO3 inorganic constituents. This study provides valuable insights into the optimization of the chemical activation step order and process parameters for enhanced specific capacitance in rice husk-derived activated carbon. These findings contribute to the development of high-performance supercapacitors using rice husk as a sustainable and cost-effective precursor material.

Graphitized mango seed as an effective 3D anode in batch and continuous mode microbial fuel cells for sustainable wastewater treatment and power generation.

Herein, we explored the utilization of graphitized mango seeds as 3D-packed anodes in microbial fuel cells (MFCs) powered by sewage wastewater. Mango seeds were graphitized at different temperatures (800 °C, 900 °C, 1000 °C, and 1100 °C) and their effectiveness as anodes was evaluated. Surface morphology analysis indicated that the proposed anode was characterized by layered branches and micro-sized deep holes, facilitating enhanced biofilm formation and microorganism attachment. Maximum power densities achieved in the MFCs utilizing the mango seed-packed anodes graphitized at 1100 °C and 1000 °C were 2170.8 ± 90 and 1350.6 ± 125 mW m-2, respectively. Furthermore, the weight of the graphitized seed anode demonstrated a positive correlation with the generated power density and cell potential. Specifically, MFCs fabricated with 9 g and 6 g anodes achieved maximum power densities of 2170.8 ± 90 and 1800.5 ± 40 mW m-2, respectively. A continuous mode air cathode MFC employing the proposed graphitized mango anode prepared at 1100 °C and operated at a flow rate of 2 L h-1 generated a stable current density of approximately 12 A m-2 after 15 hours of operation, maintaining its stability for 75 hours. Furthermore, a chemical oxygen demand (COD) removal efficiency of 85% was achieved in an assembled continuous mode MFC. Considering that the proposed MFC was driven by sewage wastewater without the addition of external microorganisms, atmospheric oxygen was used as the electron acceptor through an air cathode mode, agricultural biomass waste was employed for the preparation of the anode, and a higher power density was achieved (2170.8 mW m-2) compared to reported values; it is evident that the proposed graphitized mango seed anode exhibits high efficiency for application in MFCs.

Synergistic advancements in sewage-driven microbial fuel cells: novel carbon nanotube cathodes and biomass-derived anodes for efficient renewable energy generation and wastewater treatment.

Microbial fuel cells (MFCs) offer a dual solution of generating electrical energy from organic pollutants-laden wastewater while treating it. This study focuses on enhancing MFC performance through innovative electrode design. Three-dimensional (3D) anodes, created from corncobs and mango seeds via controlled graphitization, achieved remarkable power densities. The newly developed electrode configurations were evaluated within sewage wastewater-driven MFCs without the introduction of external microorganisms or prior treatment of the wastewater. At 1,000°C and 1,100°C graphitization temperatures, corncob and mango seed anodes produced 1,963 and 2,171 mW/m2, respectively, nearly 20 times higher than conventional carbon cloth and paper anodes. An advanced cathode composed of an activated carbon-carbon nanotube composite was introduced, rivaling expensive platinum-based cathodes. By optimizing the thermal treatment temperature and carbon nanotube content of the proposed cathode, comparable or superior performance to standard Pt/C commercial cathodes was achieved. Specifically, MFCs assembled with corncob anode with the proposed and standard Pt/C cathodes reached power densities of 1,963.1 and 2,178.6 mW/m2, respectively. Similarly, when utilizing graphitized mango seeds at 1,100°C, power densities of 2,171 and 2,151 mW/m2 were achieved for the new and standard cathodes, respectively. Furthermore, in continuous operation with a flow rate of 2 L/h, impressive chemical oxygen demand (COD) removal rates of 77% and 85% were achieved with corncob and mango seed anodes, respectively. This work highlights the significance of electrode design for enhancing MFC efficiency in electricity generation and wastewater treatment.

Kinetic analysis of p-rGO/n-TiO2 nanocomposite generated by hydrothermal technique for simultaneous photocatalytic water splitting and degradation of methylene blue dye.

In this study, the nanocomposites of reduced graphene oxide/TiO2 (rGO/TiO2 with different percentages) have been synthesized using a modified Hummers' method followed by hydrothermal treatment. The morphology and bonding structure of the prepared samples have been characterized by Fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray diffractometry (XRD), and X-ray photoelectron spectroscopy (XPS). The photo-characteristic aspects of the prepared samples have been indicated by photoluminescence (PL) emission spectroscopy and ultraviolet-visible diffuse reflection spectroscopy (DRS). The photocatalytic performance of rGO/TiO2 demonstrated that it is an effective photocatalyst for methylene blue (MB) dye decomposition through illumination by a mercury lamp. Within 60 min of continuous irradiation, the nanocomposite-induced MB decomposition reached a rate of over 99%. Different MB concentrations and optimal percent loadings in catalysts have been investigated. Furthermore, the results showed that as the amount of catalyst increased, the decomposition of MB enhanced. Finally, the loading percentage of rGO with TiO2 has been studied, and an empirical equation relating the reaction rate constant until the mass of the photocatalyst and dye concentration has been proposed. The results showed that the prepared nanocomposites had good photocatalytic activity toward water splitting and photo-decomposition of MB.

Carbon Nanofibers-Sheathed Graphite Rod Anode and Hydrophobic Cathode for Improved Performance Industrial Wastewater-Driven Microbial Fuel Cells.

Carbon nanofiber-decorated graphite rods are introduced as effective and low-cost anodes for industrial wastewater-driven microbial fuel cells. Carbon nanofiber deposition on the surface of the graphite rods could be performed by the electrospinning of polyacrylonitrile/N,N-Dimethylformamide solution using the rod as nanofiber collector, which was calcined under inert atmosphere. The experimental results indicated that at 10 min electrospinning time, the proposed graphite anode demonstrates very good performance compared to the commercial anodes. Typically, the generated power density from sugarcane industry wastewater-driven air cathode microbial fuel cells were 13 ± 0.3, 23 ± 0.7, 43 ± 1.3, and 185 ± 7.4 mW/m2 using carbon paper, carbon felt, carbon cloth, and graphite rod coated by 10-min electrospinning time carbon nanofibers anodes, respectively. The distinct performance of the proposed anode came from creating 3D carbon nanofiber layer filled with the biocatalyst. Moreover, to annihilate the internal cell resistance, a membrane-less cell was assembled by utilizing a poly(vinylidene fluoride) electrospun nanofiber layer-coated cathode. This novel strategy inspired a highly hydrophobic layer on the cathode surface, preventing water leakage to avoid utilizing the membrane. However, in both anode and cathode modifications, the electrospinning time should be optimized. The best results were obtained at 5 and 10 min for the cathode and anode, respectively.

H3PO4/KOH Activation Agent for High Performance Rice Husk Activated Carbon Electrode in Acidic Media Supercapacitors.

H3PO4/KOH combined solution is proposed as a new effective activation agent for activated carbon production from rice husk. Several activated carbon samples were produced by using different volumes of the utilized acid and alkali individually, in addition to the combined solution. FTIR results indicated that the mixed agent partially decomposed the chemical compounds on the rice husk char surface, resulting in an increase in the surface area. Moreover, XRD and EDS analyses showed the presence of a considerable amount of amorphous silica. Electrochemical measurements concluded that the volume of the activation agent solution should be optimized for both single and mixed activation agents. Numerically, for 0.3 g treated rice husk char, the maximum specific capacitance was observed at 7, 10 and 14 mL of H3PO4, KOH (3 M) and mixed (1:1 by volume) activation agents, respectively; the determined specific capacitance values were 73.5, 124.2 and 241.3 F/g, respectively. A galvanostatic charging/discharging analysis showed an approximate symmetrical triangular shape with linear voltage versus time profile which indicates very good electrochemical performance as an electrode in the supercapacitors application. The stability of the proposed activated carbon was checked by performing a cyclic voltammetry measurement for 1000 cycles at 2 mV/s and for 30,000 cycles at 10 mV/s. The results indicate an excellent specific capacitance retention, as no losses were observed.