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 ◽  
...  

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.

2006 ◽  
Vol 510-511 ◽  
pp. 750-753 ◽  
Author(s):  
Sook Young Moon ◽  
Myung Soo Kim ◽  
Hyun Sik Hahm ◽  
Yun Soo Lim

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.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Byong Chol Bai ◽  
Young-Seak Lee ◽  
Ji Sun Im

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.


2016 ◽  
Vol 45 (3) ◽  
pp. 164-171 ◽  
Author(s):  
Linjie Su ◽  
Bohong Li ◽  
Dongyu Zhao ◽  
Chuanli Qin ◽  
Zheng Jin

Purpose The purpose of this paper is to prepare a new modified activated carbon fibers (ACFs) of high specific capacitance used for electrode material of supercapacitor. Design/methodology/approach In this study, the specific capacitance of ACF was significantly increased by using the phenolic resin microspheres and melamine as modifiers to prepare modified PAN-based activated carbon fibers (MACFs) via electrospinning, pre-oxidation and carbonization. The symmetrical supercapacitor (using MACF as electrode) and hybrid supercapacitor (using MACF and activated carbon as electrodes) were tested in term of electrochemical properties by cyclic voltammetry, AC impedance and cycle stability test. Findings It was found that the specific capacitance value of the modified fibers were increased to 167 Fg-1 by adding modifiers (i.e. 20 wt.% microspheres and 15 wt.% melamine) compared to that of unmodified fibers (86.17 Fg-1). Specific capacitance of modified electrode material had little degradation over 10,000 cycles. This result can be attributed to that the modifiers embedded into the fibers changed the original morphology and enhanced the specific surface area of the fibers. Originality/value The modified ACFs in our study had high specific surface area and significantly high specific capacitance, which can be applied as efficient and environmental absorbent, and advanced electrode material of supercapacitor.


RSC Advances ◽  
2018 ◽  
Vol 8 (74) ◽  
pp. 42280-42291 ◽  
Author(s):  
Ling Zhang ◽  
Ling-yu Tu ◽  
Yan Liang ◽  
Qi Chen ◽  
Ze-sheng Li ◽  
...  

Activated carbon fibers with high micropore volume and large specific surface area were prepared from abundant and low-cost coconut fibers, which show excellent adsorption performances towards various dyes.


Processes ◽  
2021 ◽  
Vol 9 (6) ◽  
pp. 1000
Author(s):  
Ji-Hyun Kim ◽  
Gibbum Lee ◽  
Jung-Eun Park ◽  
Seok-Hwi Kim

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.


Nanomaterials ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 1313 ◽  
Author(s):  
Hye-Min Lee ◽  
Byeong-Hoon Lee ◽  
Soo-Jin Park ◽  
Kay-Hyeok An ◽  
Byung-Joo Kim

The unburned hydrocarbon (HC) emissions of automobiles are subject to strong regulations because they are known to be converted into fine dust, ozone, and photochemical smog. Pitch-based activated carbon fibers (ACF) prepared by steam activation can be a good solution for HC removal. The structural characteristics of ACF were observed using X-ray diffraction. The pore characteristics were investigated using N2/77K adsorption isotherms. The butane working capacity (BWC) was determined according to ASTM D5228. From the results, the specific surface area and total pore volume of the ACF were determined to be 840–2630 m2/g and 0.33–1.34 cm3/g, respectively. The butane activity and butane retentivity of the ACF increased with increasing activation time and were observed to range between 15.78–57.33% and 4.19–11.47%, respectively. This indicates that n-butane adsorption capacity could be a function not only of the specific surface area or total pore volume but also of the sub-mesopore volume fraction in the range of 2.0–2.5 nm of adsorbents. The ACF exhibit enhanced BWC, and especially adsorption velocity, compared to commercial products (granules and pellets), with lower concentrations of n-butane due to a uniformly well-developed pore structure open directly to the outer surface.


1990 ◽  
Vol 209 ◽  
Author(s):  
A. W. P. Fung ◽  
A. M. Rao ◽  
K. Kuriyama ◽  
M. S. Dresselhaus ◽  
G. Dresseliiaus ◽  
...  

AbstractLow-temperature electrical conductivity and Raman scattering are studied as characterization tools for activated carbon fibers, which have a high density of defects and a huge specific surface area. The transport mechanism at low temperature is governed by variablerange hopping, as in other strongly disordered systems. From the Raman spectra obtained, we deduce that the long phenolic fibers are more disordered than the acrylic fibers and that increased specific surface area corresponds to increased disorder. The average in-plane microcrystallite size is about 20–30 Å.


2007 ◽  
Vol 544-545 ◽  
pp. 31-34
Author(s):  
Jae Hong Park ◽  
Jun Ho Ji ◽  
Jeong Hoon Byeon ◽  
Gyo Woo Lee ◽  
Jung Ho Hwang

Even though activated carbon fibers (ACF) have been attractive due to high specific surface area and uniform micropore structure, there are only a few reports about the photocatalyst immobilization on ACF or their photodegradation behavior for removal of organic pollutants. In this study, ACF were selected as adsorptive support for photocatalyst immobilization. As photocatalysts, TiO2 nanoparticles were synthesized by using a N2-diluted and oxygen-enriched co-flow hydrogen diffusion flame. The visible flame length of 150mm was obtained by direct photographs. Flame temperature was measured by rapid insertion measurement technique with a R-type (Pt/Pt-13%Rd) thermocouple which was in wire shape (127μm diameter). TiO2 particles were sampled by using a high temperature particle sampler and then were coated on ACF filters. The sampling was carried out at 70mm and 110mm above the burner. The structure of TiO2 particles was analyzed by XRD. TiO2 coated ACF filters were characterized by FESEM-EDX and BET analyses. TiO2 particles on ACF filters were found to be agglomerated particles and the size of primary particles was approximately 50nm. The structure of TiO2 particle was anatase-phase crystalline structure. The specific surface area of TiO2 coated ACF filter was enhanced to be 1700~1860m2/g, depending on the sampling location, and the pores were micropores, regardless of the sampling location.


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