• 공업화학
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• 제25권2호
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• pp.193-197
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• 2014

피치계 활성탄소섬유의 유해가스 감응특성을 알아보고자 피치계 활성탄소섬유와 폴리비닐알코올(PVA)을 이용하여 가스센서용 전극을 제조하였다. 제조된 가스센서용 활성탄소섬유 전극의 물리화학적 특성은 주사전자현미경(SEM) 및 비표면적 측정기(BET)를 이용하여 분석하였다. 또한, 전극의 유해가스 감응특성은 $NH_3$, NO 및 $CO_2$와 같은 여러 유독가스를 이용하여 확인하였다. 가스센서용 활성탄소섬유 전극의 비표면적은 바인더인 PVA에 의하여 활성탄소섬유보다 33% 감소하였지만, 전극의 기공크기분포는 PVA에 의하여 크게 영향을 받지 않았다. 가스센서용 활성탄소섬유 전극은 반도체 기반 가스센서와는 다르게 전자도약에 의해서 유해가스를 감응하였다. 본 연구에서, 활성탄소섬유 전극의 저항은 100 ppm의 $NH_3$ 유해가스에 대하여 7.5% 감소하였으며, 그 $NH_3$ 가스 감응특성이 다른 유해가스보다 뛰어남을 확인하였다.

• 한국산업융합학회 논문집
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• 제26권6_3호
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• pp.1333-1339
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• 2023

To produce activated carbon fibers, the process is carried out through either physical activation method or chemical activation method. In this study, we present the results regarding the characteristics of activated carbon fibers manufactured under various conditions through the quantitative control of steam. The yield after activation indicates a decreasing trend with the increase in steam quantity and activation time. Additionally, specific surface area characteristics exhibit variations based on activation time and steam flow rate. The SEM analysis results reveal that higher steam flow rates lead to the presence of both mesopores and macropores on the surface of activated carbon fibers (ACF).

• Carbon letters
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• 제12권2호
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• pp.70-80
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• 2011

Two pitches with different average molecular structures were electrospun and compared in terms of the properties of their fibers after oxidative stabilization, carbonization, and activation. The precursor with a higher molecular weight and greater content of aliphatic groups (Pitch A) resulted in better solubility and spinnability compared to that with a lower molecular weight and lower aliphatic group content (Pitch B). The electrical conductivity of the carbon fiber web from Pitch A of 67 S/cm was higher than that from Pitch B of 52 S/cm. The carbon fiber web based on Pitch A was activated more readily with lower activation energy, resulting in a higher specific surface area compared to the carbon fiber based on Pitch B (Pitch A, 2053 $m^2/g$; Pitch B, 1374 $m^2/g$).

• Composites Research
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• 제29권5호
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• pp.256-261
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• 2016

본 연구에서는 습식공정을 이용한 Pitch계 활성탄소섬유와 바인더 섬유를 이용하여 필터 페이퍼를 제조하였다. 필터 페이퍼 내 바인더 섬유의 함량이 기공특성에 미치는 영향을 알아보기 위해 77 K에서 질소 흡착 등 온선과 주사 전자 현미경을 통해 흡착특성을 비교 분석하였다. Pitch계 활성탄소섬유와 바인더 섬유와의 최적 비율은 70:30 비율로 가장 균일한 기공 및 결합력이 좋은 페이퍼의 모습을 보였으며, 바인더 섬유의 함량이 적을수록 높은 비표면적 값을 확인하였다. Pitch계 활성탄소섬유와 바인더 섬유의 종류와는 상관없이 70:30 비율에서 최적의 페이퍼가 제조되었으며, $650.4m^2/g$의 비표면적 값과 86.9%의 유해가스 제거율을 확인하였다. 또한 필터 페이퍼의 평균 기공 크기 분포는 바인더 섬유의 영향을 받지 않는 것으로 관찰되었다.

• Carbon letters
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• 제3권2호
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• pp.93-98
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• 2002

Short pitch fibers were prepared from petroleum based isotropic precursor pitch by melt-blown technology. The pitch fibers were stabilized in oxidizing condition, followed by steam activations at various conditions. The fiber surface and pore structures of the activated carbon fibers (ACFs) were respectively characterized by using SEM and applying BET theory from nitrogen adsorption at 77 K. The weight loss of the oxidized fiber was proportional to activation temperature and activation time, independently. The adsorption isotherms of the nitrogen on the ACFs were constructed and analyzed to be as Type I consisting of micropores mainly. The specific surface area of the ACFs proportionally increased with the weight loss at a given activation temperature. The specific surface area was ranged 850~1900 $m^2/g$ with pores of narrow distribution in sizes. The average pore size was ranged 5.8~14.1 ${\AA}$ with the larger value from the more severe activation condition.

• Carbon letters
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• 제5권2호
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• pp.51-54
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• 2004

Isotropic pitch-based carbon fiber was isothermally activated in $CO_2$ atmosphere. Structural parameters of the isotropic carbon fibers and activated carbon fibers (ACFs) were evaluated by X-ray diffraction (XRD). The $d_{002}$ and La of the carbon fibers were measured to be 4.04 ${\AA}$ and 23.6 ${\AA}$ and those of ACFs were 4.29 ${\AA}$ and 22.7 ${\AA}$, respectively, representing less ordered through activation process. The pores in the ACFs were characterized by BET, and they showed super-high specific surface area of maximum value 3,495 $m^2/g$ from average pore size of 8.3 ${\AA}$ at 59% burn-off. It was recognized that 8-9 ${\AA}$ was optimum range of pore size for efficient creation of high specific surface area. The average size of the pores formed at higher temperature ($1100^{\circ}C$) was larger than that of the pores formed at lower temperature ($900^{\circ}C$).

• 한국섬유공학회:학술대회논문집
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• 한국섬유공학회 1997년도 춘계학술발표회 논문집
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• pp.323-327
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• 1997

• Carbon letters
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• 제22권
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• pp.96-100
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• 2017

• Carbon letters
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• 제1권2호
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• pp.69-75
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• 2000

Naphtha cracking bottom oil was reformed with heat treatment and then spun at $310^{\circ}C$. These pitch-based carbon fibers were carbonized at $1000^{\circ}C$ after oxidation at $280^{\circ}C$, for 90 min. These fibers were chemically activated with molar ratio of KOH/CF (1 : 1) at different temperatures ($250{\sim}900^{\circ}C$) for 1 hr. The process of activation was characterized with DTA, TGA, BET surface area and pore size distribution. The activation of fibers by KOH was performed by several process. One is the reduction process that carbon fiber was reacted with $K_2O$ produced from dehydration process above $400^{\circ}C$. The other is the process that $K_2CO_3$ was directly reacted with carbon fiber. At $800^{\circ}C$, the activation was performed by catalyzed mechanism that $K_2O$ was obtained from the reaction of metal potassium with $CO_2$, then was changed to $K_2CO_3$. At $870^{\circ}C$, the activation was also observed that activation mechanism was promoted by metal catalyst with $CO_2$ from decomposition of $K_2CO_3$. The specific surface area of prepared activated carbon fibers was dependent on the activation mechanism. The specific surface area was in the range of $1519{\sim}2000\;cm^3/g$ and was the largest prepared at $870^{\circ}C$. The pores developed were mostly micropores which was very narrow and uniform. The total pore volume was $0.58{\sim}0.77\;cm^3/g$.

• Carbon letters
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• 제6권1호
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• pp.1-5
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• 2005

Isotropic pitch based carbon fibers were exposed to isothermal oxidation in carbon dioxide gas to study the activation kinetics under the temperature of 800~$1100^{\circ}C$. The kinetic equation $f=1-{\exp}(-at^b)$ was introduced and the constant b was obtained in the range of 0.92~1.25. It was shown that the activated carbon fiber shows the highly specific surface area (SSA) when the constant b comes close to 1. The activation kinetics were evaluated by the reaction-controlling regime (RCR) according to changes of the apparent activation energy with changes of the conversion. It was observed that the activation energies increase from 47.6 to 51.2 kcal/mole with the conversion increasing from 0.2 to 0.8. It was found that the pores of the activated carbon fiber under the chemical reaction were developed well through the fiber.