scholarly journals Pistachio Shell-Derived Carbon Activated with Phosphoric Acid: A More Efficient Procedure to Improve the Performance of Li–S Batteries

Nanomaterials ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 840 ◽  
Author(s):  
Almudena Benítez ◽  
Julián Morales ◽  
Álvaro Caballero
Keyword(s):  
Phosphoric Acid ◽  
Activated Carbons ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Rate Capability ◽  
Textural Properties ◽  
Raw Material ◽  
Interconnected System ◽  
Pistachio Shell

A sustainable and low-cost lithium–sulfur (Li–S) battery was produced by reusing abundant waste from biomass as a raw material. Pistachio shell was the by-product from the agri-food industry chosen to obtain activated carbon with excellent textural properties, which acts as a conductive matrix for sulfur. Pistachio shell-derived carbon activated with phosphoric acid exhibits a high surface area (1345 m2·g−1) and pore volume (0.67 cm3·g−1), together with an interconnected system of micropores and mesopores that is capable of accommodating significant amounts of S and enhancing the charge carrier mobility of the electrochemical reaction. Moreover, preparation of the S composite was carried out by simple wet grinding of the components, eliminating the usual stage of S melting. The cell performance was very satisfactory, both in long-term cycling measurements and in rate capability tests. After the initial cycles required for cell stabilization, it maintained good capacity retention for the 300 cycles measured (the capacity loss was barely 0.85 mAh·g−1 per cycle). In the rate capability test, the capacity released was around 650 mAh·g−1 at 1C, a higher value than that supplied by other activated carbons from nut wastes.

scholarly journals Synthesis of catalysts with fine platinum particles supported by high-surface-area activated carbons and optimization of their catalytic activities for polymer electrolyte fuel cells

RSC Advances ◽  
2021 ◽  
Vol 11 (33) ◽  
pp. 20601-20611
Author(s):  
Md. Mijanur Rahman ◽  
Kenta Inaba ◽  
Garavdorj Batnyagt ◽  
Masato Saikawa ◽  
Yoshiki Kato ◽  
...  
Keyword(s):  
Fuel Cells ◽  
Polymer Electrolyte ◽  
High Performance ◽  
Activated Carbons ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Polymer Electrolyte Fuel Cells ◽  
Supported Platinum ◽  
Platinum Particles

Herein, we demonstrated that carbon-supported platinum (Pt/C) is a low-cost and high-performance electrocatalyst for polymer electrolyte fuel cells (PEFCs).

scholarly journals Synthesis of activated carbon from biowaste of fir bark for methylene blue removal

2019 ◽  
Vol 6 (9) ◽  
pp. 190523 ◽  
Author(s):  
Lu Luo ◽  
Xi Wu ◽  
Zeliang Li ◽  
Yalan Zhou ◽  
Tingting Chen ◽  
...  
Keyword(s):  
Methylene Blue ◽  
Activated Carbon ◽  
Nonlinear Models ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Raw Material ◽  
Maximum Adsorption Capacity ◽  
Koh Activation ◽  
Mb Adsorption

Activated carbon (AC) was successfully prepared from low-cost forestry fir bark (FB) waste using KOH activation method. Morphology and texture properties of ACFB were studied by scanning and high-resolution transmission electron microscopies (SEM and HRTEM), respectively. The resulting fir bark-based activated carbon (ACFB) demonstrated high surface area (1552 m 2 g −1 ) and pore volume (0.84 cm 3 g −1 ), both of which reflect excellent potential adsorption properties of ACFB towards methylene blue (MB). The effect of various factors, such as pH, initial concentration, adsorbent content as well as adsorption duration, was studied individually. Adsorption isotherms of MB were fitted using all three nonlinear models (Freundlich, Langmuir and Tempkin). The best fitting of MB adsorption results was obtained using Freundlich and Temkin. Experimental results showed that kinetics of MB adsorption by our ACFB adsorbent followed pseudo-second-order model. The maximum adsorption capacity obtained was 330 mg g −1 , which indicated that FB is an excellent raw material for low-cost production of AC suitable for cationic dye removal.

scholarly journals Jackfruit Seed-Derived Nanoporous Carbons as the Electrode Material for Supercapacitors

2020 ◽  
Vol 6 (4) ◽  
pp. 73 ◽  
Author(s):  
Rashma Chaudhary ◽  
Subrata Maji ◽  
Rekha Goswami Shrestha ◽  
Ram Lal Shrestha ◽  
Timila Shrestha ◽  
...  
Keyword(s):  
Carbon Materials ◽  
Activated Carbons ◽  
High Current Density ◽  
Chemical Activation ◽  
High Surface ◽  
High Surface Area ◽  
Rate Capability ◽  
High Specific Capacitance ◽  
High Rate ◽  
Nanoporous Carbons

Hierarchically porous activated carbon materials from agro-waste, Jackfruit seeds are prepared by a chemical activation method involving the treatment with zinc chloride (ZnCl2) at different temperatures (600–1000 °C). The electrochemical supercapacitance performances of the prepared materials were studied in an aqueous electrolyte (1 M sulfuric acid, H2SO4) in a three-electrode system. Jackfruit seed carbons display nanoporous structures consisting of both micro- and mesopore architectures and they are amorphous in nature and also contain oxygenated surface functional groups, as confirmed by powder X-ray diffraction (pXRD), Raman scattering, and Fourier-transformed infrared (FTIR) spectroscopy, respectively. The surface areas and pore volumes were found to be 1216.0 to 1340.4 m2·g−1 and 0.804 to 1.144 cm3·g−1, respectively, demonstrating the better surface textural properties compared to the commercial activated carbons. Due to the high surface area, large pore volume, and well developed hierarchical micro- and mesoporosity, the optimal sample achieved a high specific capacitance of 292.2 F·g−1 at 5 mV·s−1 and 261.3 F·g−1 at 1 A·g−1 followed by outstanding high rate capability. The electrode sustained 71.6% capacity retention at a high current density of 20 A·g−1. Furthermore, the electrode displayed exceptional cycling stability with small capacitance loss (0.6%) even after 10,000 charging–discharging cycles, suggesting that Jackfruit seed would have potential in low-cost and scalable production of nanoporous carbon materials for supercapacitors applications.

Activation of persulfate by different biochars for the degradation of sulfamethoxazole

2020 ◽  
Author(s):  
Ioannis D. Manariotis ◽  
Liana Kemmou ◽  
Elena Magioglou ◽  
Zacharias Frontistis ◽  
John Vakros ◽  
...  
Keyword(s):  
Functional Groups ◽  
Advanced Oxidation Processes ◽  
Activated Carbons ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Ultrasound Irradiation ◽  
Operating Conditions ◽  
Catalytic Supports

<p>Advanced oxidation processes (AOPs) based on persulfates have become very popular for in-situ water/wastewater treatment since persulfates are more stable and less costly than other oxidants such as hydrogen peroxide. The conversion of persulfates to sulfate radicals requires an activation agent, including transition metals, high temperature, ultraviolet irradiation, ultrasound irradiation, and microwaves. Recently, there have been several reports concerning the use of carbonaceous materials such as graphene, graphene oxide, carbon nanotubes, and activated carbons as persulfate activators. Biochars, the solid residue produced from biomass thermal decomposition with no or little oxygen at moderate temperatures, are low-cost materials with high surface area and desirable physicochemical properties in terms of pore size distribution, the number of functional groups, and minerals that can be employed as catalytic supports.</p><p>The aim of this work is to test whether biochar produced from malt spent rootlets (MSR) and olive kernels are suitable activators of persulfates for the degradation of sulfamethoxazole (SMX) under various operating conditions and aqueous matrices.  Olive kernels and MSR were pyrolyzed at 850 and 900<sup>o</sup>C, respectively.  The actual matrix effect on degradation was minor and so was the effect of radical scavengers. Persulfate activation seems to occur on the biochar surface through interactions with the surface functional groups, generating radicals that are not released in the solution.</p>

scholarly journals Chestnut-Derived Activated Carbon as a Prospective Material for Energy Storage

Materials ◽  
2020 ◽  
Vol 13 (20) ◽  
pp. 4658 ◽  
Author(s):  
Katarzyna Januszewicz ◽  
Anita Cymann-Sachajdak ◽  
Paweł Kazimierski ◽  
Marek Klein ◽  
Justyna Łuczak ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
Activated Carbons ◽  
Chemical Activation ◽  
High Surface ◽  
High Surface Area ◽  
Rate Capability ◽  
Activation Process ◽  
Porous Carbons ◽  
Subsequent Activation

In this work, we present the preparation and characterization of biomass-derived activated carbon (AC) in view of its application as electrode material for electrochemical capacitors. Porous carbons are prepared by pyrolysis of chestnut seeds and subsequent activation of the obtained biochar. We investigate here two activation methods, namely, physical by CO2 and chemical using KOH. Morphology, structure and specific surface area (SSA) of synthesized activated carbons are investigated by Brunauer-Emmett-Teller (BET) technique and scanning electron microscopy (SEM). Electrochemical studies show a clear dependence between the activation method (influencing porosity and SSA of AC) and electric capacitance values as well as rate capability of investigated electrodes. It is shown that well-developed porosity and high surface area, achieved by the chemical activation process, result in outstanding electrochemical performance of the chestnut-derived porous carbons.

Carbon Dioxide Adsorption Using High Surface Area Activated Carbons from Local Coals Modified by KOH, NaOH and ZnCl2 Agents

2017 ◽  
Vol 15 (3) ◽  
Author(s):  
Atakan Toprak ◽  
Turkan Kopac
Keyword(s):  
Surface Area ◽  
Activated Carbons ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Micropore Volume ◽  
Bet Surface Area ◽  
Dft Methods ◽  
Surface Areas ◽  
Adsorption Capacities

Abstract Activated carbons of various features were produced by the impregnation of local coal samples that were taken from Kilimli region of Zonguldak (Turkey) with chemical agents KOH, NaOH and ZnCl2 at different temperatures (600–800 °C) and concentrations (1:1–6:1 agent:coal), for their evaluation in CO2 adsorption studies. BET, DR, t-plot and DFT methods were used for the characterization of carbon samples based on N2 adsorption data obtained at 77 K. The pore sizes of activated carbons produced were generally observed to be in between 13–25 Å, containing highly micropores. Mesopore formations were higher in samples treated with ZnCl2. The highest value for the BET surface area was found as 2,599 m2 g−1 for the samples treated with KOH at 800 °C with a KOH to coal ratio of 4:1. It was observed that the CO2 adsorption capacities obtained at atmospheric pressure and 273 K were considerably affected by the micropore volume and surface area. The highest CO2 adsorption capacities were found as 9.09 mmol/g (28.57 % wt) and 8.25 mmol g−1 (26.65 % wt) for the samples obtained with KOH and NaOH treatments, respectively, at ratio of 4:1. The activated carbons produced were ordered as KOH>NaOH>ZnCl2, according to their surface areas, micropore volumes and CO2 adsorption capacities. The low-cost experimental methods developed by the utilization of local coals in this study enabled an effective capture of CO2 before its emission to atmosphere.

Phosphoric Acid Effect on Prepared Activated Carbon from Saudi Arabia’s Date Frond Waste

2011 ◽  
Vol 110-116 ◽  
pp. 2124-2130 ◽  
Author(s):  
Abdul Rahim Yacob ◽  
Hassan M. Al Swaidan
Keyword(s):  
Activated Carbon ◽  
Phosphoric Acid ◽  
Ftir Spectroscopy ◽  
Surface Area ◽  
Date Palm ◽  
Chemical Activation ◽  
High Surface ◽  
High Surface Area ◽  
Raw Material ◽  
Palm Tree

High surface area activated carbon has always fascinated researchers for its application as adsorbent, for water purification, medical and industrial. Date is the major export of Saudi Arabia, while tons of date foliar and fronds are troublesome and yet to be disposed. Transforming this waste into usable activated carbon can be a good idea for recycling, sustainable and green chemistry. In this study, date tree frond is selected to prepare activated carbon, while the effect of phosphoric acid in chemical activation is studied. Using thermogravimetry analysis, it was found that 400oC was the best temperature to convert date frond to carbon. This is supported by FTIR spectroscopy. Various concentration of phosphoric acid is used to optimize the product high surface area carbon obtained and it was found the best is at 60% phosphoric acid with the highest surface area of 1139 m2g-1. This result is also supported by FTIR spectroscopy, which indicates the similarities between commercial carbon and the carbon prepared. FESEM pictographs show chemical activation using phosphoric acid can easily open up pores and cavity of the prepared activated carbon the get the high surface area. It is thus suggested that for mass production of high surface area carbon, date palm frond is used as the source of raw material, due to its abundance and availability comes from the pruning process on the date palm tree, while chemically activated to get the high surface area.

Activated carbon from molasses efficiency for Cr(VI), Pb(II) and Cu(II) adsorption: A mechanistic study

2019 ◽  
Author(s):  
Chem Int
Keyword(s):  
Activated Carbon ◽  
Phosphoric Acid ◽  
Sugar Industry ◽  
Chemical Activation ◽  
High Surface ◽  
High Surface Area ◽  
Mechanistic Study ◽  
Acid Mixture ◽  
Maximum Adsorption Capacity ◽  
Good Potential

Activated carbon was prepared from molasses, which are natural precursors of vegetable origin resulting from the sugar industry. A simple elaboration process, based on chemical activation with phosphoric acid, was proposed. The final product, prepared by activation of molasses/phosphoric acid mixture in air at 500°C, presented high surface area (more than 1400 m2/g) and important maximum adsorption capacity for methylene blue (625 mg/g) and iodine (1660 mg/g). The activated carbon (MP2(500)) showed a good potential for the adsorption of Cr(VI), Cu(II) and Pb(II) from aqueous solutions. The affinity for the three ions was observed in the following order Cu2+ Cr6+ Pb2+. The process is governed by monolayer adsorption following the Langmuir model, with a correlation coefficient close to unity.

scholarly journals Effects of Annealing Temperature on the Oxygen Evolution Reaction Activity of Copper–Cobalt Oxide Nanosheets

Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 657
Author(s):  
Geul Han Kim ◽  
Yoo Sei Park ◽  
Juchan Yang ◽  
Myeong Je Jang ◽  
Jaehoon Jeong ◽  
...  
Keyword(s):  
High Activity ◽  
Cobalt Oxide ◽  
Oxygen Evolution ◽  
Oxygen Evolution Reaction ◽  
Low Cost ◽  
High Surface ◽  
High Surface Area ◽  
Cobalt Hydroxide ◽  
Ni Foam ◽  
Electron Conduction

Developing high performance, highly stable, and low-cost electrodes for the oxygen evolution reaction (OER) is challenging in water electrolysis technology. However, Ir- and Ru-based OER catalysts with high OER efficiency are difficult to commercialize as precious metal-based catalysts. Therefore, the study of OER catalysts, which are replaced by non-precious metals and have high activity and stability, are necessary. In this study, a copper–cobalt oxide nanosheet (CCO) electrode was synthesized by the electrodeposition of copper–cobalt hydroxide (CCOH) on Ni foam followed by annealing. The CCOH was annealed at various temperatures, and the structure changed to that of CCO at temperatures above 250 °C. In addition, it was observed that the nanosheets agglomerated when annealed at 300 °C. The CCO electrode annealed at 250 °C had a high surface area and efficient electron conduction pathways as a result of the direct growth on the Ni foam. Thus, the prepared CCO electrode exhibited enhanced OER activity (1.6 V at 261 mA/cm2) compared to those of CCOH (1.6 V at 144 mA/cm2), Co3O4 (1.6 V at 39 mA/cm2), and commercial IrO2 (1.6 V at 14 mA/cm2) electrodes. The optimized catalyst also showed high activity and stability under high pH conditions, demonstrating its potential as a low cost, highly efficient OER electrode material.

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