• Journal of the Korea Academia-Industrial cooperation Society
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• v.10 no.11
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• pp.3031-3038
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• 2009

Cobalt-loaded activated carbon fibers (ACFs) supported titanium dioxide ($TiO_2$) photocatalyst was developed by sol-gel method. The Co-ACFs/$TiO_2$ photocatalyst were characterized by scanning electron microscope (SEM), X.ray diffraction patterns (XRD), energy dispersive X.ray analysis (EDX) and UV-vis absorption spectroscopy. Decomposition efficiency of methylene blue (MB) solution by Co-ACFs/$TiO_2$ photocatalyst reached almost 100% under 300 min reaction. The MB molecules in the bulk solutions were supposed to be condensed around $TiO_2$ particles by adsorption of ACFs. Therefore, the photocatalyst possesses the combined effect of adsorption by activated carbon fibers and photocatalytic reactivity of $TiO_2$ on MB degradation. Due to the cobalt has electron transition effece, thus improved the photodegradation of MB solution.

• Journal of the Korean Electrochemical Society
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• v.5 no.3
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• pp.117-124
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• 2002

Poly(acrylonitrile)(PAN) solutions in dimethylformamide(DMF) were electrospun to prepare webs consisting of 400nm ultra-fine fibers. The webs were oxidatively stabilized, activated by steam and resulted to be activated carbon fibers(ACFs). The specific surface area was $800\~1230 m^2/g$, which showed a trend of a decrease of the surface area with an increase in activation temperature, showing opposite behavior to the other ACFs. The activation energy of the stabilized fibers for the steam activation was determined as 29.2 kJ/mol to be relatively low indicating the easier activation than that of other carbonized fibers. The ACF webs were characterized by pore size and specific surface uea which would be related to the specific capacitance of the electrical double layer capacitor (EDLC). The specific capacitances measured were 27 F/g, 25 F/g, 22 F/g at the respective activation temperature of $700^{circ}C,\;750^{\circ}C\;800^{\circ}C$, showing similar trend with the specific surface area i.e., the higher activation temperature was, the lower specific capacitance resulted.

• Journal of Korean Society of Water and Wastewater
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• v.10 no.1
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• pp.121-130
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• 1996

Adsorption isotherms of three trihalomethanes(THMs: $CHCl_3$, $CHBrCl_2$ and $CHBr_2Cl$) and the other organics(p-chlorophenol and sucrose)on activated carbon fibers(ACFs) were measured. Adsorption capacities of the ACFs for these THMs were found to be comparable with or slightly larger than those of granular activated car bons(GACs) which have been widely used for trihalomethanes control in drinking water. Also, the breakthrough curve prediction was successfully carried out using a mathematical model on basis of the assumption that the adsorption equilibrium is instantaneously established when a THM solution contacts the ACF. In practice, THM removal from drinking water was investigated at water works using benchscale ACF adsorptJOn columns. The volume of water treated at a space velocity(SV) of about $100h^{-1}$ was approximately 40 l/g-ACF. The practical adsorption capacities of PCP and sucrose in column adsorption were in good agreement with those of theoretically calculated results using the batch adsorption measurments. And the saturation time model of these substrates in the columns was also agreed succesfully with practical measurments.

• Carbon letters
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• v.27
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• pp.64-71
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• 2018

$TiO_2$-doped activated carbon fibers (ACFs) were successfully prepared as capacitive deionization (CDI) electrode materials by facile ultrasonication-assisted process. ACFs were treated with titanium isopropoxide (TTIP) and isopropyl alcohol solutions of different concentrations and then calcinated by ultrasonication without heat-treatment. The results show that a certain amount of anatase $TiO_2$ was present on the ACF surface. The specific capacitance of the $TiO_2$-doped ACF electrode was remarkably improved (by 93.8% at scan rate of $50mV\;s^{-1}$) over that of the untreated ACF electrode, despite decreases in the specific surface area and total pore volume upon $TiO_2$ doping. From the CDI experiments, the salt adsorption capacity and charge efficiency of the sample with TTIP percent concentration of 15% were found to considerably increase by 71.9 and 57.1%, respectively. These increases are attributed to the improved wettability of the electrode, which increases the number of surface active sites and facilitates salt ion diffusion in the ACF pores. Additionally, the Ti-OH groups of $TiO_2$ act as electrosorption sites, which increases the electrosorption capacity.

• Carbon letters
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• v.10 no.4
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• pp.339-344
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• 2009

Henequen fiber was air-stabilized, carbonized, and steam-activated to obtain high surface area activated henequen fiber (AHF). Thermal behavior of henequen fibers has been studied by TGA. The structural morphology and characteristics were observed by SEM and BET surface area measurement. The yield of AHF from natural henequen was in the range of 20~25 wt%. Mesopores (2~2.5 nm) were developed on the AHF as the activation temperature was raised up to $700^{\circ}C$, and the band of mesopore size distribution moved to 15~30 nm when the activation were carried out at $900^{\circ}C$ for 30 min. The specific surface area and the total pore volume were about $1394\;m^2/g$ and $1.30\;cm^3/g$, respectively at this activation conditions.

• Korean Chemical Engineering Research
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• v.62 no.1
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• pp.13-18
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• 2024

To develop flexible electrode materials for wearable devices, we investigated the electrochemical characteristics of carbon fibers tow according to pretreatment. And an electrochemical non-enzymatic sensor was fabricated using glucose as a target. The carbon fibers tow was pretreated through desizing and activation processes, and activation was performed in two ways: chemical oxidation and electrochemical oxidation. Surface morphology of carbon fibers tow samples was observed by SEM and their electrochemical characteristics and sensing performance were investigated by cyclic voltammetry, electrochemical impedance spectroscopy and chronoamperometry. Carbon fibers tow samples showed improved electrochemical properties such as reduced R_et, ΔE_p, and increased I_p through pretreatment. And similar electrochemical properties were obtained with both activation methods. We selected electrochemically activated carbon fibers tow as the final electrode material for application of electrochemical sensor. The non-enzymatic glucose sensor based on this electrode has an enhanced sensitivity of 0.744 A/mM (in a linear range of 0.09899~3.75423 mM) and 0.330 mA/mM (3.75423~50 mM), respectively. Through this study, the possibility of using carbon fibers tow was confirmed as an electrode material. It is expected to be used as basic research for development of high-performance flexible electrode materials.

• Applied Chemistry for Engineering
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• v.29 no.2
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• pp.191-195
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• 2018

In this study, the influence of microporous structures of activated carbon fibers (ACFs) on dimethyl methylphosphonate (DMMP) gas sensing properties as a nerve agent simulant was investigated. The pore structure was given to carbon fibers by chemical activation process, and an electrode was fabricated for gas sensors by using these fibers. The PAN based ACF electrode, which is an N-type semiconductor, received electrons from a reducing gas such as DMMP, and then electrical resistance of its electrode finally decreased because of the reduced density of electron holes. The sensitivity of the fabricated DMMP gas sensor increased from 1.7% to 5.1% as the micropore volume increased. It is attributed that as micropores were formed for adsorbing DMMP whose molecular size was 0.57 nm, electron transfer between DMMP and ACF was facilitated. In conclusion, it is considered that the appropriate pore structure control of ACFs plays an important role in fabricating the DMMP gas sensor with a high sensitivity.

• Journal of the Korea Concrete Institute
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• v.29 no.3
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• pp.283-290
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• 2017

Various types of fibers are utilized in cementitious materials in order to improve their performances. Here, the extent of fiber dispersion is of key importance regardless of the purpose of using fiber. In this study, activated carbon fiber dispersion in mortar samples was evaluated using electrical resistivity method. In particular, the extent of fiber dispersion was compared per mixing methods and surface treatments. The results suggest that the surface resistivity method is capable of evaluating dispersion of activated carbon fiber and that ultrasound dispersion method is superior to mortar mixer and hand mixer method. The use of superplasticizer improved dispersion but acid treatment was not effective.

• Journal of the Korean Ceramic Society
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• v.38 no.1
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• pp.1-8
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• 2001

선택적 가스분리를 위한 분자체탄소(Molecular Sieve Carbon: MSC)로서의 활용을 위해 제조된 활성탄소섬유의 흡착능과 분자체 특성이 다양한 분자크기를 갖는 가스 흡착실험을 통해 조사되었다. 각 활성화 조건별 세공크기분포와 세공발달 전개과정을 유추함으로서, 세공크기분포의 조절이 가능하게 되었으며 활성탄소섬유의 분자체 탄소로서 활용을 용이하게 할 수 있었다. 800, 85$0^{\circ}C$의 온도로 수증기에 의해 활성화한 활성탄소섬유의 경우 burn-off가 각각 50, 40% 정도를 가진 활성탄소섬유가 비교적 작은 분자크기(0.3~0.4nm)의 흡착질에 대한 분자체 특성을 나타냈다. 또한, 다양한 분자크기의 흡착질을 포함하는 혼합가스의 유속과 흡착온도의 조절로서 원하는 흡착질의 선택적 분리를 위해 활성탄소섬유가 갖는 분자체 특성 향상을 보였다.

• Carbon letters
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• v.1 no.1
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• pp.17-21
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• 2000

Catalytic reduction and oxidation of NO over polyacrylonitrile based activated carbon fibers (PAN-ACF) under various conditions were carried out to develop removal process of NO from the flue gas. The effect of temperature, oxygen concentration and the moisture content for the reduction of NO with ammonia as a reducing agent was investigated. The reduction of NO increased with the oxygen concentration, but decreased with the increased temperature. The moisture content in the flue gas affects the reduction of NO as the inhibition of the adsorption of the other components and the reaction on the surface of ACE For the oxidation of NO to $NO_2$ over PAN-ACF without using a reducing gas, it showed the temperature and the oxygen concentration of the flue gas are the important factors for the NO conversion in which the conversion increased with oxygen concentration and decreased with the temperature increase and might be the alternative option for the selective catalytic reduction process.