scholarly journals CO2 and CH4 Adsorption Behavior of Biomass Based Activated Carbons

2018 ◽  
Author(s):  
Deneb Peredo-Mancilla ◽  
Imen Ghouma ◽  
Cecile Hort ◽  
Camelia Matei Ghimbeu ◽  
Mejdi Jeguirim ◽  
...  
Keyword(s):  
Gas Adsorption ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Textural Properties ◽  
Micropore Volume ◽  
Adsorption Behavior ◽  
Bet Surface Area ◽  
Ch4 Adsorption ◽  
Oxygen Groups ◽  
Physical And Chemical

The aim of the present study is to provide new insights into the CO2 and CH4 adsorption using a set of biomass-based activated carbons obtained by physical and chemical activation of olive-stones. The adsorption behavior is analyzed by means of pure gas adsorption isotherms up to 3.2 MPa at two temperatures (303.15 and 323.15 K).The influence of the activation method on the adsorption uptake is studied in terms of both textural properties and surface chemistry. For three activated carbons the CO2 adsorption was more important than that of CH4. The chemically activation resulted in higher BET surface area and micropore volume that lead to higher adsorption for both CO2 and CH4. For methane the presence of mesopores seems to facilitate the access of the gas molecules into the micropores while for carbon dioxide, the presence of oxygen groups enhanced the adsorption capacity.

scholarly journals CO2 and CH4 Adsorption Behavior of Biomass-Based Activated Carbons

Energies ◽  
2018 ◽  
Vol 11 (11) ◽  
pp. 3136 ◽  
Author(s):  
Deneb Peredo-Mancilla ◽  
Imen Ghouma ◽  
Cecile Hort ◽  
Camelia Matei Ghimbeu ◽  
Mejdi Jeguirim ◽  
...  
Keyword(s):  
Carbon Dioxide ◽  
Activated Carbon ◽  
Adsorption Capacity ◽  
Gas Adsorption ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Textural Properties ◽  
Micropore Volume ◽  
Activation Method ◽  
Physical Activation

The aim of the present work is to study the effect of different activation methods for the production of a biomass-based activated carbon on the CO 2 and CH 4 adsorption. The influence of the activation method on the adsorption uptake was studied using three activated carbons obtained by different activation methods (H 3 PO 4 chemical activation and H 2 O and CO 2 physical activation) of olive stones. Methane and carbon dioxide pure gas adsorption experiments were carried out at two working temperatures (303.15 and 323.15 K). The influence of the activation method on the adsorption uptake was studied in terms of both textural properties and surface chemistry. For the three adsorbents, the CO 2 adsorption was more important than that of CH 4 . The chemically-activated carbon presented a higher specific surface area and micropore volume, which led to a higher adsorption capacity of both CO 2 and CH 4 . For methane adsorption, the presence of mesopores facilitated the diffusion of the gas molecules into the micropores. In the case of carbon dioxide adsorption, the presence of more oxygen groups on the water vapor-activated carbon enhanced its adsorption capacity.

Physical and Chemical Activation Effect on Activated Carbon Prepared from Local Pineapple Waste

2014 ◽  
Vol 699 ◽  
pp. 87-92 ◽  
Author(s):  
Abdul Rahim Yacob ◽  
Adlina Azmi ◽  
Mohd Khairul Asyraf Amat Mustajab
Keyword(s):  
Activated Carbon ◽  
Phosphoric Acid ◽  
Surface Area ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Bet Surface Area ◽  
Activation Effect ◽  
Pineapple Waste ◽  
Pineapple Peel ◽  
Physical And Chemical

The characteristics and quality of activated carbons prepared depending on the chemical and physical properties of the starting materials and the activation method used. In this study, activated carbon prepared using pineapple waste. Three parts of pineapple waste which comprises of peel, crown and leaf were studied. For comparison activated carbon were prepared by both physical and chemical activation respectively. Three types of chemicals were used, phosphoric acid (H3PO4), sulphuric acid (H2SO4), and potassium hydroxide (KOH). The preparation includes carbonization at 200°C and activation at the 400°C using muffle furnace. The chemical characterization of the activated carbon was carried out using Thermogravimetric analysis (TGA), Nitrogen gas adsorption analysis and Fourier transform infrared (FTIR). The highest BET surface area was achieved when the pineapple peel soaked in 20% phosphoric acid with a surface area of 1115 m2g-1. FTIR analysis indicates that the reacted pineapple waste successfully converted into activated carbons.

scholarly journals Preparation of Pore-Size Controllable Activated Carbon from Rice Husk Using Dual Activating Agent and Its Application in Supercapacitor

2019 ◽  
Vol 2019 ◽  
pp. 1-11 ◽  
Author(s):  
Khu Le Van ◽  
Thuy Luong Thi Thu
Keyword(s):  
Surface Area ◽  
Rice Husk ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Textural Properties ◽  
Micropore Volume ◽  
Scan Rate ◽  
Activating Agent ◽  
Dual Activation ◽  
A Current

Activated carbons prepared from rice husk by chemical activation with dual activation agents, KOH and NaOH, have been studied and characterized by BET, SEM, EDX, FTIR, Boehm titration, Raman, and TGA. It was found that the KOH/NaOH impregnation ratio plays an important role on textural properties of AC. At the same amount of total alkali hydroxide, the KOH/NaOH ratio higher than 1.33 resulted in larger specific surface area (2990∼3043 m2·g−1), microporous surface area (2747∼2831 m2·g−1), and higher micropore volume (1.4250∼1.4316 cm3·g−1). The as-prepared samples exist in the form of spherical-shaped particles with the size ranging from 20 to 60 nm and contain numerous surface functional groups. The as-prepared activated carbons were then assessed as an electrode material of supercapacitor operating in the 0.5 M K2SO4 electrolyte in potential windows of −1.0∼0.0 V. The highest capacitance obtained was 205 F·g−1 at the scan rate of 2 mV·s−1 and 225 F·g−1 at a current density of 0.2 A·g−1. At the scan rate as high as 50 mV·s−1, all the as-prepared activated carbons in this study have the specific capacitance greater than 100 F·g−1.

scholarly journals 3D Metal–Organic Frameworks Based on Co(II) and Bithiophendicarboxylate: Synthesis, Crystal Structures, Gas Adsorption, and Magnetic Properties

Molecules ◽  
2021 ◽  
Vol 26 (5) ◽  
pp. 1269
Author(s):  
Vadim A. Dubskikh ◽  
Anna A. Lysova ◽  
Denis G. Samsonenko ◽  
Alexander N. Lavrov ◽  
Konstantin A. Kovalenko ◽  
...  
Keyword(s):  
Room Temperature ◽  
Gas Adsorption ◽  
Magnetic Moments ◽  
Bet Surface Area ◽  
Separation Performance ◽  
Bridging Ligands ◽  
Magnetization Data ◽  
Metal Organic ◽  
Ch4 Adsorption ◽  
Gas Separation Performance

Three new 3D metal-organic porous frameworks based on Co(II) and 2,2′-bithiophen-5,5′-dicarboxylate (btdc2−) [Co3(btdc)3(bpy)2]·4DMF, 1; [Co3(btdc)3(pz)(dmf)2]·4DMF·1.5H2O, 2; [Co3(btdc)3(dmf)4]∙2DMF∙2H2O, 3 (bpy = 2,2′-bipyridyl, pz = pyrazine, dmf = N,N-dimethylformamide) were synthesized and structurally characterized. All compounds share the same trinuclear carboxylate building units {Co3(RCOO)6}, connected either by btdc2– ligands (1, 3) or by both btdc2– and pz bridging ligands (2). The permanent porosity of 1 was confirmed by N2, O2, CO, CO2, CH4 adsorption measurements at various temperatures (77 K, 273 K, 298 K), resulted in BET surface area 667 m2⋅g−1 and promising gas separation performance with selectivity factors up to 35.7 for CO2/N2, 45.4 for CO2/O2, 20.8 for CO2/CO, and 4.8 for CO2/CH4. The molar magnetic susceptibilities χp(T) were measured for 1 and 2 in the temperature range 1.77–330 K at magnetic fields up to 10 kOe. The room-temperature values of the effective magnetic moments for compounds 1 and 2 are μeff (300 K) ≈ 4.93 μB. The obtained results confirm the mainly paramagnetic nature of both compounds with some antiferromagnetic interactions at low-temperatures T < 20 K in 2 between the Co(II) cations separated by short pz linkers. Similar conclusions were also derived from the field-depending magnetization data of 1 and 2.

scholarly journals The Effects of Methane Storage Capacity Using Upgraded Activated Carbon by KOH

2018 ◽  
Vol 8 (9) ◽  
pp. 1596 ◽  
Author(s):  
Jung Park ◽  
Gi Lee ◽  
Sang Hwang ◽  
Ji Kim ◽  
Bum Hong ◽  
...  
Keyword(s):  
Surface Area ◽  
Storage Capacity ◽  
Activated Carbons ◽  
Chemical Activation ◽  
High Surface ◽  
Heat Of Adsorption ◽  
Low Grade ◽  
Surface Areas ◽  
Ch4 Adsorption ◽  
Ch4 Storage

In this study, a feasible experiment on adsorbed natural gas (ANG) was performed using activated carbons (ACs) with high surface areas. Upgraded ACs were prepared using chemical activation with potassium hydroxide, and were then applied as adsorbents for methane (CH4) storage. This study had three principal objectives: (i) upgrade ACs with high surface areas; (ii) evaluate the factors regulating CH4 adsorption capacity; and (iii) assess discharge conditions for the delivery of CH4. The results showed that upgraded ACs with surface areas of 3052 m2/g had the highest CH4 storage capacity (0.32 g-CH4/g-ACs at 3.5 MPa), which was over two times higher than the surface area and storage capacity of low-grade ACs (surface area = 1152 m2/g, 0.10 g-CH4/g-ACs). Among the factors such as surface area, packing density, and heat of adsorption in the ANG system, the heat of adsorption played an important role in controlling CH4 adsorption. The released heat also affected the CH4 storage and enhanced available applications. During the discharge of gas from the ANG system, the residual amount of CH4 increased as the temperature decreased. The amount of delivered gas was confirmed using different evacuation flow rates at 0.4 MPa, and the highest efficiency of delivery was 98% at 0.1 L/min. The results of this research strongly suggested that the heat of adsorption should be controlled by both recharging and discharging processes to prevent rapid temperature change in the adsorbent bed.

scholarly journals Biomass Valorization to Produce Porous Carbons: Applications in CO2 Capture and Biogas Upgrading to Biomethane—A Mini-Review

2021 ◽  
Vol 9 ◽  
Author(s):  
Maria Bernardo ◽  
Nuno Lapa ◽  
Isabel Fonseca ◽  
Isabel A. A. C. Esteves
Keyword(s):  
Circular Economy ◽  
Gas Adsorption ◽  
Activated Carbons ◽  
Textural Properties ◽  
Cost Effective ◽  
Attractive Alternative ◽  
Porous Carbons ◽  
Environmentally Sustainable ◽  
Gas Phases ◽  
Metal Organic

Porous carbon materials, derived from biomass wastes and/or as by-products, are considered versatile, economical and environmentally sustainable. Recently, their high adsorption capacity has led to an increased interest in several environmental applications related to separation/purification both in liquid- and gas-phases. Specifically, their use in carbon dioxide (CO2) capture/sequestration has been a hot topic in the framework of gas adsorption applications. Cost effective biomass porous carbons with enhanced textural properties and high CO2 uptakes present themselves as attractive alternative adsorbents with potential to be used in CO2 capture/separation, apart from zeolites, commercial activated carbons and metal-organic frameworks (MOFs). The renewable and sustainable character of the precursor of these bioadsorbents must be highlighted in the context of a circular-economy and emergent renewable energy market to reach the EU climate and energy goals. This mini-review summarizes the current understandings and discussions about the development of porous carbons derived from bio-wastes, focusing their application to capture CO2 and upgrade biogas to biomethane by adsorption-based processes. Biogas is composed by 55–65 v/v% of methane (CH4) mainly in 35–45 v/v% of CO2. The biogas upgraded to bio-CH4 (97%v/v) through an adsorption process yields after proper conditioning to high quality biomethane and replaces natural gas of fossil source. The circular-economy impact of bio-CH4 production is further enhanced by the use of biomass-derived porous carbons employed in the production process.

scholarly journals Pinecone-Derived Activated Carbons as an Effective Medium for Hydrogen Storage

Energies ◽  
2020 ◽  
Vol 13 (9) ◽  
pp. 2237
Author(s):  
Sara Stelitano ◽  
Giuseppe Conte ◽  
Alfonso Policicchio ◽  
Alfredo Aloise ◽  
Giovanni Desiderio ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Hydrogen Storage ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Hydrogen Adsorption ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Textural Properties ◽  
Biomass Waste ◽  
Wavelength Dispersive Spectrometry

Pinecones, a common biomass waste, has an interesting composition in terms of cellulose and lignine content that makes them excellent precursors in various activated carbon production processes. The synthesized, nanostructured, activated carbon materials show textural properties, a high specific surface area, and a large volume of micropores, which are all features that make them suitable for various applications ranging from the purification of water to energy storage. Amongst them, a very interesting application is hydrogen storage. For this purpose, activated carbon from pinecones were prepared using chemical activation with different KOH/precursor ratios, and their hydrogen adsorption capacity was evaluated at liquid nitrogen temperatures (77 K) at pressures of up to 80 bar using a Sievert’s type volumetric apparatus. Regarding the comprehensive characterization of the samples’ textural properties, the measurement of the surface area was carried out using the Brunauer–Emmett–Teller method, the chemical composition was investigated using wavelength-dispersive spectrometry, and the topography and long-range order was estimated using scanning electron microscopy and X-ray diffraction, respectively. The hydrogen adsorption properties of the activated carbon samples were measured and then fitted using the Langmuir/ Töth isotherm model to estimate the adsorption capacity at higher pressures. The results showed that chemical activation induced the formation of an optimal pore size distribution for hydrogen adsorption centered at about 0.5 nm and the proportion of micropore volume was higher than 50%, which resulted in an adsorption capacity of 5.5 wt% at 77 K and 80 bar; this was an increase of as much as 150% relative to the one predicted by the Chahine rule.

scholarly journals Changes in the Adsorption Properties of Activated Carbon due to Partial Oxidation of the Surface

1995 ◽  
Vol 12 (3) ◽  
pp. 211-219 ◽  
Author(s):  
A.M. Youssef ◽  
A.A. El-Khouly ◽  
A.I. Ahmed ◽  
E.I. El-Shafey
Keyword(s):  
Water Vapour ◽  
Surface Coverage ◽  
Activated Carbons ◽  
Textural Properties ◽  
Isosteric Heat ◽  
Adsorption Properties ◽  
Adsorption Of Water ◽  
Oxygen Groups ◽  
Initial Adsorption ◽  
Entropy Of Adsorption

The textural properties (surface area and porosity) of activated carbons change upon treatment with oxidizing solutions. The extent of this change is related to the strength of the oxidizing agent. Oxidation also changes the chemistry of the surface by forming carbon–oxygen groups which are the sites upon which the initial adsorption of water vapour takes place. The adsorption of water vapour at 300–320 K is mainly physical and the isosteric heat of adsorption decreases continuously as the surface coverage increases. The entropy of adsorption of water vapour on untreated and oxidized carbons, at different adsorption temperatures, has been calculated.

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