• Bulletin of the Korean Chemical Society
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• 제9권6호
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• pp.388-393
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• 1988

The chemisorption of CO molecules on polycrystalline nickel surface has been studied by investigating the resulting chemisorbed species with the X-ray photoelectron spectroscopy at temperatures between 300K through 433K. It is found that the adsorbed CO molecules are dissociated by the simple C-O bond cleavage as well as by the disproportionation reaction at temperatures above 373K. The former type dissociation is more favored at low coverages and at elevated temperatures. The isotherms of CO chemisorption are obtained from the xps intensities of C 1s peaks, and then the activation energy of the dissociative adsorption is estimated as a function of the CO exposure. These activation energies are extrapolated to zero coverage to obtain the activation energy of chemisorption in which thermal C-O bond cleavage takes place. The value obtained is 38.1 kJ/mol.

• 에너지공학
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• 제13권2호
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• pp.166-172
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• 2004

The activated carbon was produced from Sancheong bamboo by steam and carbon dioxide gas activation methods. The carbonization of raw material was conducted at 90$0^{\circ}C$ and gas activation reactions were conducted with respect to various conditions. -activation temperature 750-90$0^{\circ}C$, the flow rate of steam 0.5-2g-$H_2O$/g-char$.$hr, the flow rate of carbon dioxide 5-30$m\ell$-$CO_2$/g-char-min and activation time 1-5 hr. The prepared activated carbons were measured yield, the adsorption capacity of iodine and methylene blue, BET specific surface area and pore size distribution. The adsorption capacity of iodine (680.5-1526.1 mg/g) and methylene blue (18.3-221.5 mg/g) increased with creasing activation temperature and activation time. The adsorption capacity of iodine and methylene blue increased with the activation gas quantity in the range of 0.5-1.5g-$H_2O$/g-charㆍhr, 5-18.9$m\ell$-Co$_2$/g-charㆍmin. But those decreased over those range due to the pore shrinkage. The steam activation method was superior in efficiency to carbon dioxide activation method.

• 한국수소및신에너지학회논문집
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• 제34권2호
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• pp.178-186
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• 2023

Three activation methods (constant voltage, current cycling, and hydrogen pumping) were applied to investigate the effects on the performance of the membrane electrode assembly (MEA) loaded with PtCo/C catalyst. The current cycling protocol took the shortest time to activate the MEA, while the performance after activation was the worst among the all activation methods. The constant voltage method took a moderate activation time and exhibited the best performance after activation. The hydrogen pumping protocol took the longest time to activate the MEA with moderate performance after activation. According to the distribution of relaxation time analysis, the improved performance after the activation mainly comes from the decrease of charge transfer resistance rather than the ionic resistance in the cathode catalyst layer, which suggests that the existence of water on the electrode is the key factor for activation.

• Journal of Magnetics
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• 제8권3호
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• pp.108-112
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• 2003

We report the experimental finding that there exists a transition of magnetization reversal process with varying the applied field in Co/Pd multilayer. We have measured the wall-motion speed V and the nucleation rate R during magnetization reversal via time-resolved direct domain observation, where the magnetization reversal process of Co/Pd multilayer is found to take a transition from thermal activation process to viscous process at the critical field of about 1.87 H$\_$C/ (coercivity). In the thermal activation regime, we find that the field dependences of two activation volumes for the wall-motion process and the nucleation process are different with each other, which reveals that the wall-motion and nucleation experience completely different interactions. In the viscous regime, we find that the wall-mobility is much smaller than a typical value for the sandwiched Co films, which implies that the Co/Pd interfaces in multilayer substantially contribute to the dynamic dissipation.

• Carbon letters
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• 제28권
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• pp.116-120
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• 2018

Nitrogen-doped carbons have attracted much attention due to their novel application in relation to gas storage. In this study, nitrogen-doped porous carbons were synthesized using SBA-15 as a template, polypyrrole as the carbon and nitrogen precursor, and KOH as an activating agent. The effect of the activation temperature ($600-850^{\circ}C$) on the $CO_2$ adsorption capacity of the obtained porous carbons was studied. Characterization of the resulting carbons showed that they were micro-/meso-porous carbon materials with a well-developed pore structure that varied with the activation temperature. The highest surface area of $1488m^2g^{-1}$ was achieved at an activation temperature of $800^{\circ}C$ (AC-800). The nitrogen content of the activated carbon decreased from 4.74 to 1.39 wt% with an increase in the activation temperature from 600 to $850^{\circ}C$. This shows that nitrogen is oxidized and more easily removed than carbon during the activation process, which indicates that C-N bonds are more easily ruptured at higher temperatures. Furthermore, $CO_2$ adsorption isotherms showed that AC-800 exhibited the best $CO_2$ adsorption capacity of $110mg\;g^{-1}$ at 298 K and 1 bar.

• Journal of Magnetics
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• 제5권4호
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• pp.116-119
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• 2000

Magnetic field dependence of magnetization reversal in Co/Pt multilayers was quantitatively investigated. Serial samples of Co/Pt multilayers were prepared by dc-magnetron sputtering under various Ar pressures. Magnetization reversal was monitored by magnetization viscosity measurement and direct domain observation using a magneto-optical microscope system, and the wall-motion speed V and the nucleation rate R were determined using a domain reversal model based on time-resolved domain reversal patterns. Both V and R were found to be exponentially dependent on the applied reversing field. From the exponential dependencies, the activation volumes for wall motion and nucleation could be determined, based on a thermally activated relaxation model, and the wall-motion activation volume was found to be slightly larger than the nucleation activation volume.

• 한국세라믹학회지
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• 제36권10호
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• pp.1016-1021
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• 1999

활상탄소섬유는 입상 활성탄에 비해 빠른 흡 · 탈착 속도와 높은 흡착량을 갖기 때문에 흡착재, 촉매, 분자체와 같은 환경 신소재로서 큰 주목을 받고 있다. 본 연구에서는 안정화 PAN계 탄소섬유를 수증기와 CO2를 이용한 물리적 활성화에 의해 여러 등급의 활성탄소섬유를 제조하였고, 비표면적, 요오드 흡착량, 세공구조 등을 측정하였다. 수증기 활성화에서 77%의 burn-off에서 비표면적이 1019 m2/g을 나타내었고, 반면에 CO2 활성화에서는 52%의 burn-off에서 7168m2/g의 비표면적을 갖는 활성탄소섬유가 제조되었다 그러나, 비슷한 burn-off에서는 CO2로 활성화한 경우에서 세공용적이 0.37 cc/g이고, 요오드 흡착량이 1589 mg/g으로서 수증기 활성화보다 더 큰 세공용적과 요오드 흡착량을 나타내었다. 또한 제조된 활성탄소섬유의 질소 흡착등온선들은 Brunaner-Deming-Deming-Teller의 분류에 따르면 모두 type I으로 주로 미세공들로 이루어져 있음을 알 수가 있었다.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2003년도 International Meeting on Information Display
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• pp.907-909
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• 2003

We report a novel method of activation-annealing, named as induction annealing (IA). IA is realized by applying alternating electric field induced by alternatingmagnetic filed applied to the sample. We observed the enhanced kinetics of dopant activation by using IA.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1999년도 춘계학술대회 논문집
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• pp.473-476
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• 1999

PMOS capacitors with Ce-policide electrode were fabricated by the SADS method to study the effects of activation condition on the C-V characteristics. For the activation temperature of $600^{\circ}C$ , the capacitor using CoSi$_2$ formed from Co/Ti bilayer as diffusion source showed excellent C-V properties and the increase in V$_{th}$ with the increasing activation time. But impurties into the oxide.e.

• Korean Chemical Engineering Research
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• 제43권1호
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• pp.146-152
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• 2005

대나무를 원료로 이산화탄소를 활성화제로 한 기상 활성화법에 의하여 대나무 활성탄을 제조하고, 이 대나무 활성탄의 $CO_2$ 흡착 특성을 실험하였다. 국내 산청산 대나무를 탄화온도 $900^{\circ}C$에서 열분해 하여 대나무 숯을 만든 후 배치형 튜브 반응기 내에서 활성화 온도 $750-900^{\circ}C$, 이산화탄소 주입비 $5-30cm^3/g-char{\cdot}min$, 활성화 유지시간 2-5 시간의 변화 조건에서 활성화 실험을 하였다. 제조된 활성탄은 수율이 측정되고 요오드 흡착력, 메틸렌 블루 흡착력과 비표면적 및 세공분포 등의 물리적 특성이 분석되었다. $CO_2$ 흡착 실험은 열중량 분석기를 사용하여 흡착온도 $20-80^{\circ}C$, $CO_2$ 농도 5-90% 변화 조건에서 행하였다. 활성화 온도와 활성화 시간이 증가됨에 따라 요오드 흡착력(680.8-1450.1 mg/g)과 메틸렌 블루 흡착력(23.5-220 mg/g)은 증가하였다. 그리고 $CO_2$ 가스 주입량의 증가시 $18.9cm^3/g-char{\cdot}min$까지는 요오드 흡착력과 메틸렌 블루 흡착력이 증가하였으나, 그 이상에서는 과다한 반응으로 수율의 급격한 감소와 함께 요오드 흡착력과 메틸렌 블루 흡착력도 감소하였다. 대나무 활성탄 특성 분석에서 중간세공과 거대세공 부피가 $0.65-0.91cm^3/g$으로 나타나 생물활성탄공정에 유리하게 사용될 수 있다. 대나무 활성탄의 $CO_2$ 흡착 실험에서는 흡착온도 $20^{\circ}C$, $CO_2$ 농도 90%에서 최대 106 mg/g-A.C.의 $CO_2$를 물리흡착 하였다. 5회 반복 실험시 $CO_2$ 흡착 특성 변화는 없었다.