scholarly journals Influence of compressing pressure on macro void formation of carbon monolith for methane adsorption

2018 ◽  
Vol 18 (44) ◽  
pp. 24-35
Author(s):  
Narandalai B ◽  
W G Shim ◽  
M S Balathanigaimani ◽  
H Moon
Keyword(s):  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Specific Surface Area ◽  
Packing Density ◽  
Activated Carbons ◽  
Void Formation ◽  
Methyl Cellulose ◽  
Methane Adsorption ◽  
Carbon Monolith

Carbon monoliths for adsorbed natural gas (ANG) storage were prepared from Mongolian anthracite-based activated carbons using carboxy-methyl cellulose as a binder under different compressing pressures. Nitrogen adsorption/desorption experiments were carried out to obtain the specific surface area, pore volume, and pore size distribution of the monoliths.  Methane adsorption experiments on the carbon monoliths were conducted at different temperatures and pressures up to around 3.5 MPa in a high pressure volumetric adsorption apparatus. As expected, adsorption results indicated that the methane adsorption capacity of the carbon monoliths increased with increasing specific surface area and packing density.  The maximum volumetric adsorption of methane was observed as 163 V/V at 293 K and 3.5 MPa on a carbon monolith sample, PMAC1/2-3-65, that does not have the highest specific surface area but relatively high packing density comparing with other monoliths, which implies that two physical properties contribute contradictorily to the methane adsorption capacity.  Based on experimental results, the carbon monoliths prepared from Mongolian anthracite-based activated carbons can be promising media for ANG storage application.

scholarly journals Univariate and Multivariate Analyses of Influencing Factors on Methane Adsorption Capacity of Semianthracite

2021 ◽  
Vol 2021 ◽  
pp. 1-12
Author(s):  
Shihui Hou ◽  
Xiaoming Wang ◽  
Yudong Yuan ◽  
Sidong Pan ◽  
Zheng Dang ◽  
...  
Keyword(s):  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Influencing Factors ◽  
Specific Surface Area ◽  
Multivariate Analyses ◽  
Methane Adsorption ◽  
Coal Rank ◽  
Strong Positive Correlation ◽  
Quantification Theory

Methane adsorption isotherm experiments on semianthracite (2.00-2.33% R o , max ) collected from the Xin’an coal mine, Henan Province, China, were conducted to investigate the effects of pore structure, coal quality, coal maceral, and coal rank on methane adsorption capacity with applications of univariate and multivariate analyses. Methane adsorption capacity varies significantly from 12.03 to 28.40 cm3/g. In univariate analysis, methane adsorption capacity has a strong positive correlation with pore specific surface area, weak positive correlations with pore volume and ash content, and weak negative correlations with moisture content and inertinite content. No correlation is observed between methane adsorption capacity and coal rank. In multivariate analysis, the mathematical model of methane adsorption capacity affected by the combined individual variables is established based on quantification theory I. There are similarities and differences between the two analyses. The similarities are that pore specific surface area has the greatest contribution to methane adsorption capacity, while coal rank has the least contribution. The differences are reflected in two aspects. Firstly, the other influencing factors contribute differently to methane adsorption capacity. Secondly, the positive or negative correlations of some influencing factors present the opposite. The mathematic model synthetically covers the combined effects of the influencing factors, which is more representative in evaluating methane adsorption capacity.

Study of the Porous Structure and High Adsorption Capacity of Biomass-Based Activated Carbon Prepared from Aspen Wood by Ferric Nitrate III Activation

2021 ◽  
Vol 15 (2) ◽  
pp. 131-144
Author(s):  
Chunjiang Jin ◽  
Huimin Chen ◽  
Luyuan Wang ◽  
Xingxing Cheng ◽  
Donghai An ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Mass Ratio ◽  
Aspen Wood ◽  
Surface Functional Groups ◽  
Wood Sawdust

In this study, aspen wood sawdust was used as the raw material, and Fe(NO3)3 and CO2 were used as activators. Activated carbon powder (ACP) was produced by the one-step physicochemical activation method in an open vacuum tube furnace. The effects of different mass ratios of Fe(NO3)3 and aspen wood sawdust on the pore structure of ACP were examined under single-variable experimental conditions. The mass ratio was 0–0.4. The detailed characteristics of ACP were examined by nitrogen adsorption, scanning electron microscopy, X-ray diffraction, and Fourier transform infrared spectroscopy. The adsorption capacity of ACP was established by simulating volatile organic compounds (VOCs) using ethyl acetate. The results showed that ACP has a good nanostructure with a large pore volume, specific surface area, and surface functional groups. The pore volume and specific surface area of Fe-AC-0.3 were 0.26 cm3/g and 455.36 m2/g, respectively. The activator played an important role in the formation of the pore structure and morphology of ACP. When the mass ratio was 0–0.3, the porosity increased linearly, but when it was higher than 0.3, the porosity decreased. For example, the pore volume and specific surface area of Fe-AC-0.4 reached 0.24 cm3/g and 430.87 m2/g, respectively. ACP presented good VOC adsorption performance. The Fe-AC-0.3 sample, which contained the most micropore structures, presented the best adsorption capacity for ethyl acetate at 712.58 mg/g. Under the action of the specific reaction products nitrogen dioxide (NO2) and oxygen, the surface of modified ACP samples showed different rich C/O/N surface functional groups, including C-H, C=C, C=O, C-O-C, and C-N.

Investigation of the methane adsorption characteristics of marine organic-rich shale: A case study of the lower Cambrian Niutitang Shale in the Fenggang block, northern Guizhou Province, South China

2018 ◽  
Vol 6 (4) ◽  
pp. T819-T833 ◽  
Author(s):  
Yang Gu ◽  
Wenlong Ding ◽  
Min Yin ◽  
Ruyue Wang ◽  
Baocheng Jiao ◽  
...  
Keyword(s):  
Specific Surface ◽  
Pore Size ◽  
Adsorption Capacity ◽  
Surface Area ◽  
South China ◽  
Pore Volume ◽  
Lower Cambrian ◽  
Methane Adsorption ◽  
Guizhou Province ◽  
Average Value

The marine shale in South China has great gas exploration potential, and exploration in the Sichuan Basin has been successful, but the degree of exploration remains low in the Guizhou Province. We used organic geochemical analyses (total organic carbon content and kerogen type), scanning electron microscopy (SEM), field emission SEM, nuclear magnetic resonance (NMR), X-ray diffraction analysis, and low-temperature [Formula: see text] and [Formula: see text] adsorption experimental methods to study the micropore types and pore structures and their effects on the methane adsorption capacity of organic-rich shales found in the Fenggang block in northern Guizhou Province. The results indicate that the microscopic surface porosity of the lower Cambrian Niutitang Formation ranges from 2.88% to 5.34%, with an average value of 3.86%. Based on nitrogen adsorption methods, the range of the average pore size distribution is 4.6–9.491 nm, with an average value of 6.68 nm. All of the samples exhibit significant unimodal distributions. The main pore size is less than 10 nm, and these pores account for most of the mesopore volume, which is generally consistent with the NMR results. The methane adsorption capacity of the shale samples gradually increases in the range of 0–8 MPa at 30°C and reaches a maximum at approximately 10 MPa. Positive correlations were found between the gas content and specific surface area, total pore volume, and micropore volume. These strong correlations indicate that the Niutitang Shale has a high specific surface area, a high pore volume, and narrow-diameter pores, demonstrating that it has a high gas adsorption capacity. The results of this study provide valuable information regarding the adsorption characteristics of marine shales and the factors that affect those characteristics.

scholarly journals Adsorption of Ammonium Nitrogen from Aqueous Solution on Chemically Activated Biochar Prepared from Sorghum Distillers Grain

2019 ◽  
Vol 9 (23) ◽  
pp. 5249 ◽  
Author(s):  
Derlin Hsu ◽  
Changyi Lu ◽  
Tairan Pang ◽  
Yuanpeng Wang ◽  
Guanhua Wang
Keyword(s):  
Aqueous Solution ◽  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Specific Surface Area ◽  
Adsorption Process ◽  
Ammonium Nitrogen ◽  
Activated Biochar ◽  
Distillers Grain ◽  
Kinetics And Isotherms

Chemically activated biochars prepared from sorghum distillers grain using two base activators (NaOH and KOH) were investigated for their adsorption properties with respect to ammonium nitrogen from aqueous solution. Detailed characterizations, including scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetry (TG), and specific surface area analyses, were carried out to offer a broad evaluation of the prepared biochars. The results showed that the NaOH- and KOH-activated biochars exhibited significantly enhanced adsorption capacity, by 2.93 and 4.74 times, respectively, in comparison with the pristine biochar. Although the NaOH-activated biochar possessed larger specific surface area (132.8 and 117.7 m2/g for the NaOH- and KOH-activated biochars, respectively), the KOH-activated biochar had higher adsorption capacity owing to its much higher content of functional groups. The adsorption kinetics and isotherms of the KOH-activated biochar at different temperatures were further studied. The biochar had a maximum adsorption capacity of 14.34 mg/g at 45 °C, which was satisfactory compared with other biochars prepared using different feedstocks. The adsorption process followed pseudo-second-order kinetics, and chemical adsorption was the rate-controlling step. The equilibrium data were consistent with the Freundlich isotherm, and the thermodynamic parameters suggested that the adsorption process was endothermic and spontaneous. Consequently, this work demonstrates that chemically activated biochar from sorghum distillers grain is effective for ammonium nitrogen removal.

scholarly journals Activated Carbons from Thermoplastic Precursors and Their Energy Storage Applications

Nanomaterials ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 896 ◽  
Author(s):  
Hye-Min Lee ◽  
Kwan-Woo Kim ◽  
Young-Kwon Park ◽  
Kay-Hyeok An ◽  
Soo-Jin Park ◽  
...  
Keyword(s):  
Electron Microscope ◽  
Specific Surface ◽  
Surface Area ◽  
Field Emission ◽  
Specific Surface Area ◽  
Pore Volume ◽  
Activated Carbons ◽  
Total Pore Volume ◽  
Cross Linking ◽  
Mesopore Volume

In this study, low-density polyethylene (LDPE)-derived activated carbons (PE-AC) were prepared as electrode materials for an electric double-layer capacitor (EDLC) by techniques of cross-linking, carbonization, and subsequent activation under various conditions. The surface morphologies and structural characteristics of the PE-AC were observed by field-emission scanning electron microscope, Cs-corrected field-emission transmission electron microscope, and X-ray diffraction analysis, respectively. The nitrogen adsorption isotherm-desorption characteristics were confirmed by Brunauer–Emmett–Teller, nonlocal density functional theory, and Barrett–Joyner–Halenda equations at 77 K. The results showed that the specific surface area and total pore volume of the activated samples increased with increasing the activation time. The specific surface area, the total pore volume, and mesopore volume of the PE-AC were found to be increased finally to 1600 m2/g, 0.86 cm3/g, and 0.3 cm3/g, respectively. The PE-AC also exhibited a high mesopore volume ratio of 35%. This mesopore-rich characteristic of the activated carbon from the LDPE is considered to be originated from the cross-linking density and crystallinity of precursor polymer. The high specific surface area and mesopore volume of the PE-AC led to their excellent performance as EDLC electrodes, including a specific capacitance of 112 F/g.

scholarly journals Effects of Wet Oxidation Process on Biochar Surface in Acid and Alkaline Soil Environments

Materials ◽  
2018 ◽  
Vol 11 (12) ◽  
pp. 2362 ◽  
Author(s):  
Qinya Fan ◽  
Liqiang Cui ◽  
Guixiang Quan ◽  
Sanfei Wang ◽  
Jianxiong Sun ◽  
...  
Keyword(s):  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Functional Groups ◽  
Specific Surface Area ◽  
Contaminated Soils ◽  
Soil Conditions ◽  
Acid Oxidation ◽  
Wet Oxidation ◽  
Alkaline Soil

Biochar has been studied for remediation of heavy metal-contaminated soils by many researchers. When in external conditions, biochar in soils ages, which can transform its structural properties and adsorption capacity. This study was conducted with two oxidation processes, HNO3/H2SO4 and NaOH/H2O2, to simulate the effects of biochar in acid and alkaline soil conditions. The results show that the oxygen-containing functional groups increased in aged biochar, which led to improve the ratio of oxygen and carbon (O/C). Nitro functional groups were found in the acid-oxidation treated biochar. Destroyed ditches and scars were observed on the surface of aged biochar and resulted in growth in their specific surface area and porosity. Specific surface area increased by 21.1%, 164.9%, and 63.0% for reed-derived biochar treated with water washing, acid oxidation, and basic oxidation, respectively. Greater peaks in the Fourier Transform Infrared Spectroscopy (FTIR) results were found in C–O and O–H on the surface of field-aged biochar. Meanwhile, mappings of energy-dispersive spectroscopy showed that biochar aged in soil was abundant in minerals such as silicon, iron, aluminum, and magnesium. In summary, biochar subjected to wet oxidation aging had an increased capacity to immobilize Cd compared to unaged biochar, and the adsorption capacity of oxidized biochar increased by 28.4% and 13.15% compared to unaged biochar due to improvements in porosity and an increase in functional groups.

Using Activated Diatomite as Adsorbent for Treatment of Arsenic Contaminated Water

2020 ◽  
Vol 850 ◽  
pp. 16-21
Author(s):  
Hoc Thang Nguyen ◽  
Phong Thanh Dang
Keyword(s):  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Specific Surface Area ◽  
Contaminated Water ◽  
Viet Nam ◽  
High Porosity ◽  
Room Condition ◽  
Main Chemical Composition ◽  
Adsorbent Capacity

Diatomite or diatomaceous earth (DE) is one of materials which can be used as an adsorbent to treat heavy metal ions from waste water, even there are many factories used it to clean the water for drinking. However, natural DE (raw DE) has very low adsorption capacity because of low specific surface area. In this work, natural DE from Lam Dong province, Viet Nam was demagnetized to remove iron and activated by HCl solution for 90 minutes with concentration of 10% at room condition. Adsorbent capacity was evaluated using As solution and the results show that the activated diatomite has adsorption capacity three times higher than that of raw DE, and the specific surface area of activated diatomite was increased 47.5% with the main chemical composition of 90.8% SiO2 and high porosity

scholarly journals Improve in CO2 and CH4 Adsorption Capacity on Carbon Microfibers Synthesized by Electrospinning of PAN

Fibers ◽  
2019 ◽  
Vol 7 (10) ◽  
pp. 81 ◽  
Author(s):  
Reyna Ojeda-López ◽  
J. Marcos Esparza-Schulz ◽  
Isaac J. Pérez-Hermosillo ◽  
Armin Hernández-Gordillo ◽  
Armando Domínguez-Ortiz
Keyword(s):  
Specific Surface ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Specific Surface Area ◽  
Gas Adsorption ◽  
Morphological Structure ◽  
Different Temperatures ◽  
Ch4 Adsorption ◽  
Stabilization Temperature ◽  
Carbon Microfibers

Carbon microfibers (CMF) has been used as an adsorbent material for CO2 and CH4 capture. The gas adsorption capacity depends on the chemical and morphological structure of CMF. The CMF physicochemical properties change according to the applied stabilization and carbonization temperatures. With the aim of studying the effect of stabilization temperature on the structural properties of the carbon microfibers and their CO2 and CH4 adsorption capacity, four different stabilization temperatures (250, 270, 280, and 300 °C) were explored, maintaining a constant carbonization temperature (900 °C). In materials stabilized at 250 and 270 °C, the cyclization was incomplete, in that, the nitrile groups (triple-bond structure, e.g., C≡N) were not converted to a double-bond structure (e.g., C=N), to form a six-membered cyclic pyridine ring, as a consequence the material stabilized at 300 °C resulting in fragile microfibers; therefore, the most appropriate stabilization temperature was 280 °C. Finally, to corroborate that the specific surface area (microporosity) is not the determining factor that influences the adsorption capacity of the materials, carbonization of polyacrylonitrile microfibers (PANMFs) at five different temperatures (600, 700, 800, 900, and 1000 °C) is carried, maintaining a constant temperature of 280 °C for the stabilization process. As a result, the CMF chemical composition directly affects the CO2 and CH4 adsorption capacity, even more directly than the specific surface area. Thus, the chemical variety can be useful to develop carbon microfibers with a high adsorption capacity and selectivity in materials with a low specific surface area. The amount adsorbed at 25 °C and 1.0 bar oscillate between 2.0 and 2.9 mmol/g adsorbent for CO2 and between 0.8 and 2.0 mmol/g adsorbent for CH4, depending on the calcination treatment applicated; these values are comparable with other material adsorbents of greenhouse gases.

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