• 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 $m^2/g$).

• 공업화학
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• 제28권6호
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• pp.638-644
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• 2017

전기이중층 커패시터(electric double layer capacitor, EDLC) 전극용 핏치계 활성탄소섬유의 고출력 특성을 향상시키기 위하여 불소와 산소 혼합가스의 다양한 불소분압에 따라 함산소불소화 표면처리를 수행하였다. 함산소불소화 처리된 핏치계 활성탄소섬유는 불소 부분압이 증가함에 따라 선형적인 불소관능기의 증가를 보였고, 산소관능기는 증가하였으나 부분압에 따라 차이가 없었다. 또한 함산소불소화를 통하여 활성탄소섬유 표면의 식각 반응으로 인하여 비표면적 및 기공부피는 감소하였으나 중간기공 부피는 약 4.5배 증가하였다. 50%의 불소가스 분압으로 처리한 활성탄소섬유의 경우 5와 50 mV/s의 전압주입속도에서 비정전용량이 약 29%와 61%로 증가함을 확인하였다. 이러한 비정전용량의 향상은 함산소불소화 처리를 통한 활성탄소섬유 표면의 산소 및 불소 관능기의 도입과 중간기공의 증가에 의한 효과로 사료된다.

• Carbon letters
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• 제27권
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• pp.112-116
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• 2018

• 한국재료학회지
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• 제13권11호
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• pp.749-755
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• 2003

A development of micropores of $CO_2$activated isotropic carbon fibers from TEM was observed. It was observed that the micropores of activated carbon fibers(ACFs) were consisted of slit-shaped pores(SP) and cylinder-shaped pores(CP). The SPs were formed between two parallel-carbon layers, and the CPs were formed at a place which is connected polygonally by more than two carbon layers. It was shown that the CPs of the ACFs were developed at high degree of burn-offs and at high activation temperature. The pore size distribution of the best ACF, which was observed at a highest value of specific surface area(3,495 $\m^2$/g), showed a continuous distribution in the range of about $4∼l5\AA$, and the median pore size was 6.7$\AA$. The super-high specific surface area of ACFs was found to be due to that the SPs were connected with a maximum size of 7∼8$\AA$ continuously, It is possible that the SPs should be formed in the ACFs in order to show super-high SSA.

• 한국세라믹학회:학술대회논문집
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• 한국세라믹학회 2002년도 추계총회 및 연구발표회 초록집
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• pp.209.1-209
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• 2002

• Carbon letters
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• 제15권1호
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• pp.1-14
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• 2014

Carbon nanofibers (CNFs) with diameters in the submicron and nanometer range exhibit high specific surface area, hierarchically porous structure, flexibility, and super strength which allow them to be used in the electrode materials of energy storage devices, and as hybrid-type filler in carbon fiber reinforced plastics and bone tissue scaffold. Unlike catalytic synthesis and other methods, electrospinning of various polymeric precursors followed by stabilization and carbonization has become a straightforward and convenient way to fabricate continuous CNFs. This paper is a comprehensive and brief review on the latest advances made in the development of electrospun CNFs with major focus on the promising applications accomplished by appropriately regulating the microstructural, mechanical, and electrical properties of as-spun CNFs. Additionally, the article describes the various strategies to make a variety of carbon CNFs for energy conversion and storage, catalysis, sensor, adsorption/separation, and biomedical applications. It is envisioned that electrospun CNFs will be the key materials of green science and technology through close collaborations with carbon fibers and carbon nanotubes.

• Carbon letters
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• 제6권4호
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• pp.248-254
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• 2005

Silver impregnated activated carbon fibers were post-modified using hydrochloric acid. Adsorption behaviors, SEM morphologies, and functional groups for the silver impregnated ACFs were compared with those of post-modified ACFs. Adsorption isotherms were used to characterize $S_{BET}$, the pore structure and volume of silver-activated carbon fibers (ACFs) before and after acid post-treatment. In order to the reveal the causes of the differences surface states after the samples were washed with hydrochloric acid, outer surface and pore structure were investigated by SEM. And the type and quality of various functional groups were studied from FT-IR spectra and Boehm titration method. Finally, the quantitative properties in silver contents were also examined by EDX spectra.

• Carbon letters
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• 제3권3호
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• pp.146-151
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• 2002

Activated carbon fibers were prepared from the petroleum isotropic pitch and organometallic compounds. The metalsvwere dispersed uniformly in the ACFs. The specific surface area and pore size distributions of metal containing ACFsvwere measured. The mesopores of ACFs were developed by Co, Ni, and Mn metals addition and the catalytic reactivityvof ACFs'SOx removal was increased by adding Ni and Pd metals. It was found that the mesopores did not work forvthe improvement of catalytic reactivity of ACFs' SOx removal with the blank experiment using the metal removedvACFs.

• 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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• 제6권4호
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• pp.243-247
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• 2005

Plasma polymerization of allylamine subsequently after plasma pre-treatment was conducted on the activated carbon fibers (ACFs) for the immobilization of amine groups in the surface of ACFs. The change of structural properties of ACFs with respect to different polymerization conditions was investigated through BET method. The change of surface morphologies of ACFs with respect to different plasma polymerization power was also studied through AFM. It was found that the structural properties such as specific surface area and micropore volume could be optimized under certain plasma deposition conditions. It was reckoned that treatment and deposition showed adverse effect on plasma polymerization, in which the former developed the micro-structures of the ACFs and the latter tended to block the micro pores. The Fourier transform infrared spectroscopy (FTIR) revealed that the poly(allylamine) was successfully immobilized on the surface of ACFs and the amount of the deposited polymer layer was related to the plasma polymerization power. SEM results showed that the plasma deposited polymer layer were small and homogenously distributed. The size and the distribution of particles deposited were closely related to the plasma polymerization power, too.