• Carbon letters
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• 제16권1호
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• pp.19-24
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• 2015

The breakthrough behaviour of activated charcoal cloth samples against an oxygen analogue (OA) of sulphur mustard has been studied using the modified Wheeler equation. Activated charcoal cloth samples having different surface area values in the range of 481 to $1290m^2/g$ were used for this purpose. Breakthrough behaviour was found to depend on the properties of the activated charcoal cloth, properties of the OA and the adsorption conditions. Activated charcoal cloth with a high surface area of $1290m^2/g$, relatively large surface density of $160g/m^2$ and coarser fiber structure exhibited better kinetic saturation capacity value, 0.19 g/g, against OA vapours when compared to others, thus confirming its potential use in foldable masks for protection against chemical warfare agents.

• 한국응용과학기술학회지
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• 제22권1호
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• pp.43-49
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• 2005

OXI-PAN fibers, Kynol fibers and rayon fibers were used as precursorsfor the preparation of activated carbon fibers (ACFs) by chemical activation with KOH at $800^{\circ}C$. The effects of different precursorfibers and fiber/KOH ratios on the final ACFs are discussed. The precursor fibers used are appropriate for the ACFs in a single stage pyrolysis process. The OXI-PAN fibers which were activated with KOH of 2.0M showed a specific surface area of $2328m^2/g$ however, loosed the fiber shape because of low yields. The Kynol fibers and Rayon fibers showed the high yields but the lower specific surface area of $900m^2/g$ and $774m^2/g$, respectively, at KOH of 1.5M. The OXI-PAN fibers which were activated with KOH of 1.5M have a specific surface area of $1028m^2/g$ and higher micro-pore volumes and lower yields rather than Kynol-1.5 and Rayon-1.5 samples. This phenomenon is because of higher chemical resistance of the Kynol and Rayon fibers rather than OXI-PAN fibers. However, the Kynol fibers were the best precursors on KOH activation at $800^{\circ}C$ considered carbon yields, surface areas and micropore volumes.

• 한국연초학회지
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• 제27권1호
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• pp.59-67
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• 2005

Activated carbon fiber (ACF) was surface modified by nitric acid to improve the adsorption efficiency of the propylamine. The adsorption amount of propylamine of the modified ACF increased $17\%$ more than that of as-received ACF. Desorption of propylamine from the propylamine saturated ACF was occurred in two steps, the first step started arround $50^{\circ}C$ showing the desorption of physically adsorbed propylamine and the second step started at $200^{\circ}C$ showing the decomposition of chemically adsorbed propylamine. Total desorption amount of propylamine from the modified ACF was larger than that of the as-received ACF because of increased functional groups. The oxygen and nitrogen contents on the modified ACF increased by 1.5 and 3 times compared with the as-received ACF. A part of propylamine adsorbed on ACF formed pyridine-like or pyrrolic structures with 2 carbons exposed on the surface of the ACF. It was found that propylamine reacted with strong or weak acidic functional groups such as -COOH or -OH existed on ACF surface.

• 한국연초학회지
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• 제31권1호
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• pp.9-17
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• 2009

Activated carbon fiber (ACF) was surface modified by nitric acid to improve the adsorption efficiency of the propylamine. Functional groups and textural properties of modified ACF were investigated. The total surface acidity increased about 7 times to that of as-received ACF by modification with 1 M nitric acid solution, carboxylic and phenolic groups mainly increased. However, the specific surface areas and the total pore volumes of the modified ACFs were decreased by 5-8% due to the increased blocking (or demolition) of micropores in the presence of newly introduced complexes. Despite the decrease of textural properties, it was found that the amount of propylamine adsorbed by the modified ACFs was increased by approximately 17%. The oxygen and nitrogen contents on the modified ACF increased by 1.5 and 3 times compared with the as-received ACF. From the XPS results, it was observed that propylamine reacted with strong or weak acidic groups, such as -COOH or -OH on the ACF surfaces, resulting in the formation of pyrrolic-, pyridonic- or pyridine-like structures.

• 한국대기환경학회지
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• 제20권5호
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• pp.655-662
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• 2004

An adsorption process to recover the pure $CH_4\;and\;CO_2$ from its mixture was examined. In this study, activated carbon fibers were used as a selective adsorbent. The activated carbon fibers has 78~94% micropore volume and 10.5~20.3${\AA}$ narrow pore size, and showed high adsorption rate and the good selectivity for $CO_2$ under the ambient pressure. The ACF with high surface area showed short mass transfer zone and long breakthrough time and, its adsorption capacity depended on the microporosity. Compared with single component adsorption, the amount adsorbed $CO_2$ on ACF increased by the roll-up of $CH_4$ in mixed gases. The adsorption selectivity increased as now rate and $CO_2$ concentration of mixed gases increased, showing 5.2 selectivity for 75% $CO_2$ concentration.

• 공업화학
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• 제4권1호
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• pp.113-124
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• 1993

Polyacrylonitrile계 섬유를 전구체로 하여 비등온 과정에 의한 활성화를 승온속도를 달리한 TGA(thermogravimetric analysis) 방법으로 연구하였다. 탄소섬유 -$H_2O$(30%)-$N_2$계 비등온 활성화 과정에서 유도된 속도식 $f=1-\exp(-a{\Delta}T)^b$는 실험값과 잘 일치하였다. 전환율에 따른 세공 용적은 pore volume model에 의한 이론값과 비교적 잘 일치하였고, 이때의 세공 구조는 승온속도, 활성화 온도와 내부 및 외부 전환율과의 복합적인 작용에 의하여 결정되었다.

• 융복합기술연구소 논문집
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• 제12권1호
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• pp.13-18
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• 2022

Polyacrylonitrile was synthesized through suspension polymerization and then sieved to obtain spherical beads with a size of 200~510 ㎛. PAN was copolymerized with 2 mol% MMA monomer which is known to promote cyclization and crosslinking of nitrile group. The resonance cyclization reaction of the nitrile group in the synthesized PAN beads was observed near 170℃ with thermal analysis and FT-IR. The reaction conversion of the nitrile group in spherical beads was 23% during heat treatment, which was lower than that of the well-oriented PAN fiber used as a precursor of carbon fiber. This is because the stereo-regularity of molecular chains in the form of a random coil (spherical bead) is much lower than that of PAN fiber. It was confirmed that the compressive strength of the spherical PAN bead was greatly improved through the resonance cyclization and shrinkage according to the heat treatment, and it was also observed that the pores in PAN beads were formed after the heat treatment.

• 한국재료학회지
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• 제32권2호
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• pp.107-113
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• 2022

Fibrous supercapacitors (FSs), owing to their high power density, good safety characteristic, and high flexibility, have recently been in the spotlight as energy storage devices for wearable electronics. However, despite these advantages, FCs face many challenges related to their active material of carbon fiber (CF). CF has low surface area and poor wettability between electrode and electrolyte, which result in low capacitance and poor long-term stability at high current densities. To overcome these limits, fibrous supercapacitors made using surface-activated CF (FS-SACF) are here suggested; these materials have improved specific surface area and better wettability, obtained by introducing porous structure and oxygen-containing functional groups on the CF surface, respectively, through surface engineering. The FS-SACF shows an improved ion diffusion coefficient and better electrochemical performance, including high specific capacity of 223.6 mF cm^-2 at current density of 10 ㎂ cm^-2, high-rate performance of 171.2 mF cm^-2 at current density of 50.0 ㎂ cm^-2, and remarkable, ultrafast cycling stability (96.2 % after 1,000 cycles at current density of 250.0 ㎂ cm^-2). The excellent electrochemical performance is definitely due to the effects of surface functionalization on CF, leading to improved specific surface area and superior ion diffusion capability.

• 한국세라믹학회지
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• 제38권10호
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• pp.928-935
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• 2001

본 연구에서는 PAN계 안정화섬유를 원료로 하여 수증기를 이용한 물리적 활성화에 의해 여러 등급의 활성탄소섬유를 제조하고, 비표면적, 요오드 흡착량, 미세구조, 세공구조 등을 측정하여 제조조건에 따른 그 특성변화를 고찰하였다. 수증기를 이용한 물리적 활성화에서 기존의 탄화과정과 활성화과정의 2단계를 이용한 공정과, 탄화공정과 활성화 공정을 동시에 수행하는 1단계 활성화과정을 비교함으로써 저가로 활성탄소섬유를 제조할 수 있는 제조방법을 연구하였다. 2단계 법에서는 안정화 섬유를 $900^{\circ}C$에서 탄화한 후 이를 다시 $900^{\circ}C$에서 활성화하는 방법으로 $1019m^2/g$의 비표면적을 갖는 활성탄소섬유를 얻었으나 1단계 방법에서는 $900^{\circ}C$에서 $1636m^2/g$의 비표면적을 갖는 활성탄소섬유를 제조하였다. 이들 활성탄소섬유 사이에는 비표면적, 요오드 흡착력, 기공분포 등이 서로 차이가 있음에도 불구하고, Brunauer-Deming-Deming-Teller(BDDT)에 의한 분류에서는 제I형을 나타내는 공통점도 가지고 있었다.

• 공업화학
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• 제10권6호
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• pp.822-827
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• 1999

본 연구에서는 에너지 밀도가 큰 초고용량 캐패시터를 제작하기 위한 기초 연구로서 활성탄소섬유의 물성과 유기 전해질의 특성이 초고용량 캐패시터의 전기화학적 특성에 미치는 영향을 조사하였다. 유기성 전해질의 경우는 이온의 크기가 수용성 전해질 보다 훨씬 크기 때문에 탄소전극의 세공크기에 많은 영향을 받으며, 용량을 발현할 수 있는 유효세공의 크기가 커야 한다는 것을 알 수 있었다. 혼합용매를 이용한 전해액의 조성은 큰 비축전용량과 빠른 충전속도, 그리고 낮은 ESR 및 방전전류의 세기에 대한 높은 비축전용량 유지성 등의 우수한 충방전 특성을 나타내는 것을 알 수 있었고, 전해질의 높은 이온전도도가 용량발현 및 자가방전 특성에 큰기여를 하고 있으며, 전해질 이온의 크기는 충전속도에 많은 영향을 미치는 것을 알 수 있었다.