scholarly journals Characterization of Chemically and Physically Activated Carbons from Lignocellulosic Ethanol Lignin-Rich Stream via Hydrothermal Carbonization and Slow Pyrolysis Pretreatment

Energies ◽  
2020 ◽  
Vol 13 (16) ◽  
pp. 4101
Author(s):  
Edoardo Miliotti ◽  
Luca Rosi ◽  
Lorenzo Bettucci ◽  
Giulia Lotti ◽  
Andrea Maria Rizzo ◽  
...  
Keyword(s):  
Specific Surface ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Morphological Characteristics ◽  
Value Added ◽  
Total Pore Volume ◽  
Hydrothermal Carbonization ◽  
Physical Activation ◽  
Lignocellulosic Ethanol ◽  
Slow Pyrolysis

The aim of the present work is to investigate the possibility of producing activated carbons from the residual lignin stream of lignocellulosic ethanol biorefineries, as this represents an optimal opportunity to exploit a residual and renewable material in the perspective of sustainable bioeconomy, increasing biorefinery incomes by producing value-added bioproducts in conjunction with biofuels. Activated carbons (ACs) were produced via chemical (KOH) and physical (CO2) activation. Char samples were obtained by slow pyrolysis (SP) and hydrothermal carbonization (HTC). Several HTC experiments were carried out by varying residence time (0.5–3 h) and reaction temperature (200–270 °C), in order to evaluate their influence on the product yield and on the morphological characteristics of the hydrochar (specific surface area, total pore volume and pore size distribution). ACs from hydrochars were compared with those obtained from pyrochar (via physical activation) and from the raw lignin-rich stream (via chemical activation). In both cases, by increasing the HTC temperature, the specific surface of the resulting activated carbons decreased from 630 to 77 m2 g−1 for physical activation and from 675 to 81 m2 g−1 for chemical activation, indicating that an increase in the severity of the hydrothermal pretreatment is deleterious for the activated carbons quality. In addition, the HTC aqueous samples were analyzed, with GC-MS and GC-FID. The results suggest that at low temperatures the reaction mechanisms are dominated by hydrolysis, instead when the temperature is increased to 270 °C, a more complex network of reactions takes place among which decarboxylation.

scholarly journals Highly Porous Carbons Synthesized from Tannic Acid via a Combined Mechanochemical Salt-Templating and Mild Activation Strategy

Molecules ◽  
2021 ◽  
Vol 26 (7) ◽  
pp. 1826
Author(s):  
Sylwia Głowniak ◽  
Barbara Szczęśniak ◽  
Jerzy Choma ◽  
Mietek Jaroniec
Keyword(s):  
Specific Surface ◽  
Tannic Acid ◽  
Activated Carbons ◽  
Low Cost ◽  
Chemical Activation ◽  
Total Pore Volume ◽  
Co2 Uptake ◽  
Potassium Oxalate ◽  
Templating Method ◽  
Highly Porous

Highly porous activated carbons were synthesized via the mechanochemical salt-templating method using both sustainable precursors and sustainable chemical activators. Tannic acid is a polyphenolic compound derived from biomass, which, together with urea, can serve as a low-cost, environmentally friendly precursor for the preparation of efficient N-doped carbons. The use of various organic and inorganic salts as activating agents afforded carbons with diverse structural and physicochemical characteristics, e.g., their specific surface areas ranged from 1190 m2·g−1 to 3060 m2·g−1. Coupling the salt-templating method and chemical activation with potassium oxalate appeared to be an efficient strategy for the synthesis of a highly porous carbon with a specific surface area of 3060 m2·g−1, a large total pore volume of 3.07 cm3·g−1 and high H2 and CO2 adsorption capacities of 13.2 mmol·g−1 at −196 °C and 4.7 mmol·g−1 at 0 °C, respectively. The most microporous carbon from the series exhibited a CO2 uptake capacity as high as 6.4 mmol·g−1 at 1 bar and 0 °C. Moreover, these samples showed exceptionally high thermal stability. Such activated carbons obtained from readily available sustainable precursors and activators are attractive for several applications in adsorption and catalysis.

scholarly journals Use of sawdust Eucalyptus sp. in the preparation of activated carbons

2012 ◽  
Vol 36 (1) ◽  
pp. 69-77 ◽  
Author(s):  
Gabriela Martucci Couto ◽  
Anelise Lima de Abreu Dessimoni ◽  
Maria Lúcia Bianchi ◽  
Deise Morone Perígolo ◽  
Paulo Fernando Trugilho
Keyword(s):  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Physical Activation ◽  
Elementary Analysis ◽  
Aqueous Effluents ◽  
Adsorption Desorption ◽  
Eucalyptus Sawdust

Wood sawdust is a solid residue, generated in the timber industry, which is of no profitable use and can cause serious environmental problems if disposed inadequately. The aim of this study was to use the eucalyptus sawdust in the preparation of activated carbons AC) and test them as adsorbents of methylene blue (MB) and phenol, representative pollutants from aqueous effluents of various industries. The eucalyptus sawdust was characterized by instrumental analysis such as elementary analysis (CHNS-O), thermogravimetric analysis (TGA), infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). The activated carbons were prepared by physical activation with carbon dioxide AC_CO2, (10º C min-1, 850º C, 1h) and by chemical activation with potassium carbonate AC_K2CO3 (10º C min-1, 850º C, 3h). The AC_CO2 and AC_K2CO3 were characterized by CHN-O, TGA, FTIR, N2 adsorption/desorption (BET) to evaluate the specific surface area and SEM. The resulting activated carbons were tested for their ability to adsorb MB and phenol in water. The activated carbons produced in this work were predominantly microporous and showed specific surface area of about 535 m² g-1. The AC_K2CO3 was more effective in the adsorption of MB (81 mg g-1) and phenol (330 mg g-1) than AC_CO2 (32 mg g-1 and 172 mg g-1, respectively, for MB and phenol).

scholarly journals Activated Carbon from Winemaking Waste: Thermoeconomic Analysis for Large-Scale Production

Energies ◽  
2020 ◽  
Vol 13 (23) ◽  
pp. 6462
Author(s):  
Isaac Lorero ◽  
Arturo J. Vizcaíno ◽  
Francisco J. Alguacil ◽  
Félix A. López
Keyword(s):  
Activated Carbon ◽  
Heat Exchangers ◽  
Large Scale ◽  
Activated Carbons ◽  
Hydrothermal Carbonization ◽  
Thermodynamic Efficiency ◽  
Physical Activation ◽  
Scale Production ◽  
Production Scale ◽  
Costs Analysis

An activated carbon manufacturing process from winemaking waste is analyzed. In that way, vine shoots conversion is studied as a basis for plant designing, and mass and energy balances of hydrothermal carbonization and physical activation are fulfilled. To develop an energy-integrated plant, a network of heat exchangers is allocated to recover heat waste, and a cogeneration cycle is designed to provide electricity and remaining heat process demands. Furthermore, thermoeconomic analysis is applied to determine the thermodynamic efficiency and the economic viability of the plant. Energy balance indicates that heat exchangers energy integration covers 48.9% of the overall demands by crossing hot and cold streams and recovering heat from residual flue gas. On the other hand, the exergy costs analysis identifies combustion of pruning wood as the main source of exergy destruction, confirming the suitability of the integration to improve the thermodynamic performance. Attending to economic costs analysis, production scale and vineyard pruning wood price are identified as a critical parameter on process profitability. With a scale of 2.5 ton/h of pruning wood carbonization, a break-event point to compete with activated carbons from biomass origin is reached. Nevertheless, cost of pruning wood is identified as another important economic parameter, pointing out the suitability of wet methods such as hydrothermal carbonization (HTC) to treat them as received form the harvest and to contribute to cutting down its prices.

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 Regeneration of Activated Carbons Spent by Waste Water Treatment Using KOH Chemical Activation

2019 ◽  
Vol 9 (23) ◽  
pp. 5132 ◽  
Author(s):  
Jung Eun Park ◽  
Gi Bbum Lee ◽  
Bum Ui Hong ◽  
Sang Youp Hwang
Keyword(s):  
Waste Water ◽  
Heat Treatment ◽  
Water Treatment ◽  
Specific Surface ◽  
Surface Area ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Waste Water Treatment ◽  
Waste Water Treatment Plant ◽  
X Ray

In this study, spent activated carbons (ACs) were collected from a waste water treatment plant (WWTP) in Incheon, South Korea, and regenerated by heat treatment and KOH chemical activation. The specific surface area of spent AC was 680 m2/g, and increased up to 710 m2/g through heat treatment. When the spent AC was activated by the chemical agent potassium hydroxide (KOH), the surface area increased to 1380 m2/g. The chemically activated ACs were also washed with acetic acid (CH3COOH) to compare the effect of ash removal during KOH activation. The low temperature N2 adsorption was utilized to measure the specific surface areas and pore size distributions of regenerated ACs by heat treatment and chemical activation. The functional groups and adsorbed materials on ACs were also analyzed by X-ray photoelectron spectroscopy and X-ray fluorescence. The generated ash was confirmed by proximate analysis and elementary analysis. The regenerated ACs were tested for toluene adsorption, and their capacities were compared with commercial ACs. The toluene adsorption capacity of regenerated ACs was higher than commercial ACs. Therefore, it is a research to create high value-added products using the waste.

scholarly journals Highly Porous Graphitic Activated Carbons from Lignite via Microwave Pretreatment and Iron-Catalyzed Graphitization at Low-Temperature for Supercapacitor Electrode Materials

Processes ◽  
2019 ◽  
Vol 7 (5) ◽  
pp. 300 ◽  
Author(s):  
Dongdong Liu ◽  
Xiaoman Zhao ◽  
Rui Su ◽  
Zhengkai Hao ◽  
Boyin Jia ◽  
...  
Keyword(s):  
Low Temperature ◽  
Electrode Materials ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Scale Up ◽  
Physical Activation ◽  
Supercapacitor Electrode ◽  
Microwave Pretreatment ◽  
Wide Range ◽  
Highly Porous

At present, the preparation of highly porous graphitic activated carbons (HPGACs) using the usual physical and chemical activation methods has met a bottleneck. In this study, HPGACs are directly synthesized from lignite at 900 °C. The whole process is completed by a microwave pretreatment, a graphitization conversion of the carbon framework at a low temperature using a small amount of FeCl3 (10–30 wt%), and a subsequent physical activation using CO2. Consequently, the dispersed and mobile iron species, in the absence of oxygen functional groups (removed during the microwave pretreatment), can greatly promote catalytic graphitization during pyrolysis, and, as an activating catalyst, can further facilitate the porosity development during activation. The as-obtained AC-2FeHLH-5-41.4(H) presents a low defect density, high purity, and specific surface area of 1852.43 m2 g−1, which is far greater than the AC-HLH-5-55.6(H) obtained solely by physical activation. AC-2FeHLH-5-41.4(H) as a supercapacitor electrode presents an excellent performance in the further electrochemical measurements. Such a convenient and practical method with low cost proves a scalable method to prepare HPGACs from a wide range of coal/biomass materials for industrial scale-up and applications.

scholarly journals Characterization and comparison of walnut shells-based activated carbons and their adsorptive properties

2020 ◽  
Vol 38 (9-10) ◽  
pp. 450-463
Author(s):  
Xiya Li ◽  
Jieqiong Qiu ◽  
Yiqi Hu ◽  
Xiaoyuan Ren ◽  
Lu He ◽  
...  
Keyword(s):  
Adsorption Capacity ◽  
Activated Carbons ◽  
Low Cost ◽  
Total Pore Volume ◽  
Textural Properties ◽  
Hydrothermal Carbonization ◽  
Bet Surface Area ◽  
Activation Process ◽  
Walnut Shells ◽  
Adsorption Desorption

The production of low-cost biologically activated carbons (BACs) is urgent need of environmental protection and ecological sustainability. Hence, walnut shells were treated by traditional pyrolysis, direct KOH impregnation and combined activation composed of hydrothermal carbonization and two-step H3PO4- and pyrolysis-activation process to obtain porous carbon with high adsorption capacity. It was found that the best adsorption capacity for iodine and organic dye methylene blue (MB) can be obtained using the KOH impregnation at impregnation ratio of 1:1 or combined activation comprising of 2 h H3PO4 activation and 1 h pyrolysis activation at 1000°C. The produced KOH, H3PO4/pyrolysis activated BACs at the optimum conditions are superior to that of commercial ACs, 9.4 and 1.3 times for MB removal, 4 and 4.5 times for iodine number respectively. Characterization results demonstrated their porous structure with very good textural properties such as high BET surface area (1689.1 m2/g, 1545.3 m2/g) and high total pore volume (0.94 cm3/g, 0.96 cm3/g). The N2 adsorption-desorption isotherm of H3PO4/pyrolysis activated hydrochar suggested the co-existence of micro and meso-pores. Moreover, they are more effective for the removal of Fe(III) and Cr(VI) from aqueous solution than the commercial AC, suggesting a promising application in the field of water treatment.

Preparation of activated carbons from wet activated sludge by direct chemical activation

2009 ◽  
Vol 59 (12) ◽  
pp. 2387-2394 ◽  
Author(s):  
X. Wang ◽  
N. Zhu ◽  
J. Xu ◽  
B. Yin
Keyword(s):  
Activated Carbon ◽  
Activated Sludge ◽  
Water Content ◽  
Iodine Value ◽  
Activated Carbons ◽  
Chemical Activation ◽  
Total Pore Volume ◽  
Processing Parameters ◽  
Experimental Conditions ◽  
Activation Temperature

An improved method for preparing activated carbons from wet waste activated sludge (WAS) by direct chemical activation was studied in this paper. The effects of processing parameters on iodine adsorption capacity of the product were investigated. Results show that sludge-based activated carbon prepared with KOH had a larger iodine value than those activated with ZnCl2 and KCl. The maximum iodine value was observed at the KOH concentration of 0.50 M. Increasing the impregnation time from 10 to 20 h resulted in a 20% increase in the iodine value. The highest iodine value was obtained at the activation temperature of 600°C and holding time of 1 h. Sludge water content had insignificant effects on the iodine value of products. Raw WAS with a water content of 93.2% can be converted into an activated carbon with a high specific surface area of 737.6 m2 g−1 and iodine value of 864.8 mgg−1 under optimum experimental conditions. Other physical properties such as total pore volume, micropore volume and mean pore diameter of the product were also reported and compared with those of commercial activated carbon.

Comparison on the Characteristics of Bio-Based Porous Carbons by Physical and Novel Chemical Activation

2014 ◽  
Vol 554 ◽  
pp. 22-26 ◽  
Author(s):  
Jibril Mohammed ◽  
Noor Shawal Nasri ◽  
Muhammad Abbas Ahmad Zaini ◽  
Usman Hamza Dadum ◽  
Murtala Musa Ahmed
Keyword(s):  
Activated Carbon ◽  
Surface Area ◽  
Chemical Activation ◽  
Value Added ◽  
Potassium Acetate ◽  
Lower Surface ◽  
Physical Activation ◽  
Porous Carbons ◽  
Surface Areas ◽  
Agricultural Materials

There is significantly abundant portion of waste agricultural materials in the world serving as environmental challenge, however, they could be converted into useful value added products like activated carbon. Coconut shell based carbons were synthesized using physical activation by CO2 and chemical activation with potassium hydroxide and potassium acetate. The BET surface areas and pore volumes are 361m2/g and 0.19cm3/g for physical activation, 1353m2/g and 0.61cm3/g for activation with KOH and 622m2/g and 0.31cm3/g for potassium acetate activated carbon. From the Fourier Transform Infrared Spectroscopy analysis, hydroxyls, alkenes and carbonyl functional groups were identified with more prominence on the chemically activated porous carbons. Thermogravimetric analysis (TGA) results showed occurrence of moisture pyrolysis at 105°C, the pyrolysis of hemicellulose and cellulose occurred at 160–390°C and lignin at (390-650°C). Carbonization at 700°C and 2hrs had highest yield of 32%. Physical activation yielded lower surface area with approximately 88% micropores. On the other hand, chemically activation yielded higher surface area with elevated mesopores. The porous carbons can be applied to salvage pollution challenges.

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