scholarly journals Limitation of K2CO3 as a Chemical Agent for Upgrading Activated Carbon

Processes ◽  
2021 ◽  
Vol 9 (6) ◽  
pp. 1000
Author(s):  
Ji-Hyun Kim ◽  
Gibbum Lee ◽  
Jung-Eun Park ◽  
Seok-Hwi Kim
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Alkali Metals ◽  
Chemical Activation ◽  
Molar Ratio ◽  
Chemical Agent ◽  
Carbon Precursor ◽  
High Concentration

The chemical activation of a carbon precursor with KOH generally results in an activated carbon (AC) with a high specific surface area. However, this process generates a large volume of wastewater that includes dissolved alkali metals, existing mainly as K2CO3. Thus, wastewaters with a high concentration of dissolved K2CO3 can potentially be used in place of KOH as a chemical agent. In the present study, to reduce the thermal stability of K2CO3, which decomposes at temperatures greater than 891 °C, K2CO3 was chemically impregnated into carbon precursors prior to activation of the precursors. The thermochemical properties and activation efficiency of the carbon precursors treated with K2CO3 were compared with those of carbon precursors treated with KOH. Analysis by XPS indicated that C–O–K complexes formed on the surface of the carbon precursors; in addition, their peak intensities were approximately the same irrespective of the chemical agent used. However, the specific surface area of the K2CO3-impregnated AC was 2162 m2/g, which was ~70% of that of the KOH-impregnated AC (3047 m2/g) prepared using the same K/C molar ratio of 0.5. XRD results confirmed that both K2CO3 and KOH transformed into KHCO3 and K4H2(CO3)3·1.5H2O during the impregnation. The peak intensities of these compounds in the XRD pattern of the K2CO3-impregnated carbon precursors were two times greater than those in the pattern of the KOH-impregnated carbon precursors. These compounds eventually transformed into K2CO3, which hardly participated as a chemical agent at the temperature used in the present study (850 °C). Therefore, recrystallisation of K2CO3, even during the impregnation, appeared to adversely affect the degree of activation. Nevertheless, the specific surface area of the K2CO3-activated AC was still ~1.6 times greater than that of the untreated carbon precursor (1378 m2/g), suggesting that the use of wastewater as a chemical agent is feasible for resource recycling.

Fabrication of Activated Carbon Fibers from Stabilized PAN-Based Fibers by KOH

2004 ◽  
Vol 449-452 ◽  
pp. 217-220 ◽  
Author(s):  
Young Jae Lee ◽  
Jae Hyung Kim ◽  
Jang Soon Kim ◽  
Dong Bok Lee ◽  
Jae Chun Lee ◽  
...  
Keyword(s):  
Experimental Data ◽  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Fibers ◽  
Potassium Hydroxide ◽  
Chemical Activation ◽  
Activated Carbon Fibers ◽  
High Concentration

Activated carbon fibers were prepared from stabilized PAN-based fibers by chemical activation using potassium hydroxide at different concentration. The experimental data showed variations in specific surface area, microstructure by the activated carbon fibers. Specific surface area of about 2545 m2/g was obtained in the KOH/stabilized PAN-based fiber ratio of 1:1 at 800°. An abrupt reduction of specific surface area was observed in the experiments with the ratio of 3:1 of OH/stabilized PAN-based fiber, being dissimilar with the result of KOH/fiber ratios of 1:1 and 2:1 in the similar experiments. The high concentration of KOH led to the destruction of micropore walls instead of forming mesopores.

Production and characterization of lignocellulosic biomass-derived activated carbon

2010 ◽  
Vol 62 (11) ◽  
pp. 2637-2646 ◽  
Author(s):  
A. B. Namazi ◽  
C. Q. Jia ◽  
D. G. Allen
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Lignocellulosic Biomass ◽  
Specific Surface Area ◽  
Chemical Activation ◽  
Pulp Mill ◽  
Activation Process ◽  
Activation Temperature ◽  
Biomass Ratio

The goal of this work is to establish the technical feasibility of producing activated carbon from pulp mill sludges. KOH chemical activation of four lignocellulosic biomass materials, two sludges from pulp mills, one sludge for a linerboard mill, and cow manure, were investigated experimentally, with a focus on the effects of KOH/biomass ratio (1/1, 1.5/1 and 2/1), activation temperature (400–600°C) and activation time (1 to 2 h) on the development of porosity. The activation products were characterized for their physical and chemical properties using a surface area analyzer, scanning electron microscopy and Fourier transform infrared spectroscopy. Experiments were carried out to establish the effectiveness of the lignocellulosic biomass-derived activated carbon in removing methylene blue (MB), a surrogate of large organic molecules. The results show that the activated carbon are highly porous with specific surface area greater than 500 m2/g. The yield of activated carbon was greater than the percent of fixed carbon in the dry sludge, suggesting that the activation process was able to capture a substantial amount of carbon from the organic matter in the sludge. While 400°C was too low, 600°C was high enough to sustain a substantial rate of activation for linerboard sludge. The KOH/biomass ratio, activation temperature and time all play important roles in pore development and yield control, allowing optimization of the activation process. MB adsorption followed a Langmuir isotherm for all four activated carbon, although the adsorption capacity of NK-primary sludge-derived activated carbon was considerably lower than the rest, consistent with its lower specific surface area.

scholarly journals Production of Activated Carbon with High Specific Surface Area from Bean-curd Refuse by Chemical Activation

TANSO ◽  
1996 ◽  
Vol 1996 (172) ◽  
pp. 95-99 ◽  
Author(s):  
Katsuhiko Muroyama ◽  
Jun'ichi Hayashi ◽  
Atsushi Sato ◽  
Susumu Takemoto
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Chemical Activation ◽  
High Specific Surface Area

scholarly journals Preparation of Activated Carbon from Desiccated Coconut Residue by Chemical Activation with NaOH

2015 ◽  
Vol 5 (1) ◽  
pp. 24 ◽  
Author(s):  
Mohd Adib Yahya ◽  
C. W. Zanariah C. W. Ngah ◽  
M. A. Hashim ◽  
Z. Al-Qodah
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Agricultural Waste ◽  
Chemical Activation ◽  
Nitrogen Atmosphere ◽  
Effect Of Temperature ◽  
Impregnation Ratio ◽  
Different Temperatures

<p class="1Body">This study investigates the effect of temperature and impregnation ratio on the physicochemical properties of activated carbon prepared from agricultural waste; desiccated coconut residue (DCR) by chemical activation using sodium hydroxide (NaOH). DCR sample was first carbonized at three different temperatures for 1 hour at 400°C, 500°C, and 600°C respectively. The resulting chars were impregnated with NaOH at three different impregnation ratio; 1:1, 1:2, and 1:3 respectively and activated under nitrogen atmosphere for 1 hour at three different temperatures based on its carbonization temperature. The specific surface area was strongly affected by impregnation ratio in which increased with impregnation ratio. The specific surface area also increased with temperature but then decreased at highest desired temperature.</p>

Preparation of Activated Carbon Fibers by Chemical Activation Method with Hydroxides

2006 ◽  
Vol 510-511 ◽  
pp. 750-753 ◽  
Author(s):  
Sook Young Moon ◽  
Myung Soo Kim ◽  
Hyun Sik Hahm ◽  
Yun Soo Lim
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Fibers ◽  
Chemical Activation ◽  
Lower Surface ◽  
Activation Process ◽  
Temperature Profiles ◽  
Activated Carbon Fibers

Activated carbon fibers were prepared from stabilized PAN-based fibers by chemical activation using hydroxides at different concentrations. The experimental data showed variations in specific surface area, microstructure, pore size distribution, and amounts of iodine adsorbed by the activated carbon fibers. Specific surface area of about 2244m2/g and iodine adsorption of 1202mg/g were obtained in the KOH 1.5M. However, the use of NaOH in the activation process rather than KOH and using the same time/ temperature profiles resulted in a carbon with a much lower surface area. KOH is a more developed pore structure than NaOH, which means that KOH is a better activation agent in producing ACF than NaOH.

Production of activated carbon with high specific surface area from bean-curd refuse by chemical activation

Carbon ◽  
1996 ◽  
Vol 34 (9) ◽  
pp. 1164
Author(s):  
Katsuhiko Muroyama ◽  
Jun'ichi Hayashi ◽  
Atsushi Sato ◽  
Susumu Takemoto
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Chemical Activation ◽  
High Specific Surface Area

scholarly journals Activated carbon fibers for toxic gas removal based on electrical investigation: Mechanistic study of p-type/n-type junction structures

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Byong Chol Bai ◽  
Young-Seak Lee ◽  
Ji Sun Im
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Fibers ◽  
Chemical Activation ◽  
Mechanistic Study ◽  
Activated Carbon Fibers ◽  
Gas Removal ◽  
P Type

Abstract In this study, we evaluated the potential use of CuO-ZnO combination structures with activated carbon fibers (ACFs) for the adsorption (by ACFs) and electrochemical detection (by CuO-ZnO) by of SO2 gas. The gas adsorptivity was concluded to improve as a result of the synergetic effects of physical adsorption by the micropores and mesopores, the specific surface area developed by chemical activation and the chemical adsorption reaction between SO2 and the transition metals introduced in the CuO-ZnO combination structures. From comparison of the SO2 sensing properties, the CuO-ZnO combination structures with ACFs exhibited the fastest sensing capability. This result can be attributed to the larger specific surface area of the semiconductor, which extended its depletion layer by forming p-type CuO/n-type ZnO junctions. This phenomenon led to good SO2 detection through a decrease in the resistance; thus, the contributions of the sensing responses of p-type CuO and n-type ZnO represent a predominant characteristic of the sensor. These types of mechanisms were proven through various physicochemical and electrical characterization methods, especially through evaluation of the SO2 sensing capability of the CuO-ZnO combination structures with ACFs. The reversible sensing capability indicates that the p-n junction structure changed the electrical properties of the ACFs, leading to an intriguing sensing mechanism.

scholarly journals Experimental Study on Activated Carbon-MIL-101(Cr) Composites for Ethanol Vapor Adsorption

Materials ◽  
2021 ◽  
Vol 14 (14) ◽  
pp. 3811
Author(s):  
Zhongbao Liu ◽  
Jiayang Gao ◽  
Xin Qi ◽  
Zhi Zhao ◽  
Han Sun
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Ethanol Vapor ◽  
Future Application ◽  
Working Fluid ◽  
Relative Pressure ◽  
Adsorption Refrigeration ◽  
Vapor Adsorption

In this study, the hydrothermal method was used to synthesize MIL-101(Cr), and activated carbon (AC) with different content was incorporated in to MIL-101(Cr), thereby obtaining AC-MIL-101(Cr) composite material with a huge specific surface area. The physical properties of MIL-101(Cr) and AC-MIL-101(Cr) were characterized by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), thermogravimetric analysis (TGA), nitrogen adsorption and desorption and specific surface area testing, and ethanol vapor adsorption performance testing. The results show that with the increase of activated carbon content, the thermal stability of AC-MIL-101(Cr) is improved. Compared with the pure sample, the BET specific surface area and pore volume of AC-MIL-101(Cr) have increased; In the relative pressure range of 0–0.4, the saturated adsorption capacity of AC-MIL-101(Cr) to ethanol vapor decreases slightly. It is lower than MIL-101(Cr), but its adsorption rate is improved. Therefore, AC-MIL-101(Cr)/ethanol vapor has a good application prospect in adsorption refrigeration systems. The exploration of AC-MIL-101(Cr) composite materials in this paper provides a reference for the future application of carbon-based/MOFS composite adsorbent/ethanol vapor working fluid in adsorption refrigeration.

Increase the Microporosity and CO2 Adsorption of a Commercial Activated Carbon

2015 ◽  
Vol 749 ◽  
pp. 17-21 ◽  
Author(s):  
Joanna Sreńscek Nazzal ◽  
Karolina Glonek ◽  
Jacek Młodzik ◽  
Urszula Narkiewicz ◽  
Antoni W. Morawski ◽  
...  
Keyword(s):  
Activated Carbon ◽  
Specific Surface ◽  
Surface Area ◽  
Specific Surface Area ◽  
Carbon Materials ◽  
Micropore Volume ◽  
Microporous Carbon ◽  
Microporous Carbons ◽  
Adsorption Capacities

Microporous carbons prepared from commercial activated carbon WG12 by KOH and/or ZnCl2 treatment were examined as adsorbents for CO2 capture. The micropore volume and specific surface area of the resulting carbons varied from 0.52 cm3/g (1374 m2/g) to 0.70 cm3/g (1800 m2/g), respectively. The obtained microporous carbon materials showed high CO2 adsorption capacities at 40 bar pressure reaching 16.4 mmol/g.

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