• 한국고분자학회:학술대회논문집
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• 한국고분자학회 2006년도 IUPAC International Symposium on Advanced Polymers for Emerging Technologies
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• pp.155-155
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• 2006

The most commercially and academically advanced catalysts of late transition metals are diimine complexes based on Pd(II)/Ni(II) and bis(imino)pyridyl complexes based on Fe(II)/Co(II). It is well known that the former systems yield branched polyethylenes and the latter linear PEs. In this presentation, effect of extremely bulky ligands with electron withdrawing/donating substituents at a remote position from Ni(II) metal center and of using multi-nuclear homo or hetero multi-metal on the ethylene polymerization is to be paged.

• 소성∙가공
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• 제13권2호
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• pp.174-179
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• 2004

The effect of grain refinement on the plastic deformation behaviour of nanocrystalline metallic materials is investigated. A phase mixture model in which a single phase material is considered as an effectively two-phase one is discussed. A distinctive feature of the model is that grain boundaries are treated as a separate phase deforming by a diffusion mechanism. For the grain interior phase two concurrent mechanisms are considered: dislocation glide and mass transfer by diffusion. The proposed constitutive model was implemented into a finite element code (DEFORM) using a semicoupled approach. The finite element method was applied to simulating room temperature tensile deformation of Cu down to the nanoscale grain size in order to investigate the pre- and post-necking behaviour.

• 세라미스트
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• 제21권4호
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• pp.416-426
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• 2018

Water splitting is regarded as one of the most environmentally benign routes for hydrogen production. Nevertheless, the low energy efficiency to produce the hydrogen has been a critical bottleneck, which is attributable to the multi-electron and multi-step reactions during water splitting reaction. In this respect, the development of efficient, durable, and inexpensive catalysts that can promote the reaction is indispensable. Extensive searching for new catalysts has been carried out for past decades, identifying several promising catalysts. Recently, researchers have found that conventional battery materials; particularly high-voltage intercalation-based cathode materials, could exhibit remarkable performance in catalyzing the water splitting process. One of the unique capabilities in this class of materials is that the valency state of metals and the atomic arrangement of the structure can be easily tailored, based on simple intercalation chemistry. Moreover, taking advantage of the rich prior knowledge on the intercalation compounds can offer the unexplored path to identify new water splitting catalysts.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2002년도 춘계학술발표회 초록집
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• pp.37-37
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• 2002

Diamoncl/Mo/Ni multi-layers on SKH-51 steel substrate was prepared to improve the abrasive wear resistance of a tool and die by a commercial chemical vapor deposition unit and electro-plating. The diamond after 7 hour deposition had cuba-octahedral structure with 2~5$\mu\textrm{m}$ grains. The existence of non-ferrous metals such as chromium, nickel and molybdenum between diamond and SKH-51 substrate results in forming higher quality of diamond layer by retarding carbon diffusion in the diamond layer during deposition, and also improving hardness and wear resistance. Surface cracks on the film was sometimes observed by the difference of by the thermal expansion coefficients between the steel substrate and the deposited layers during cooling.

• 자원리싸이클링
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• 제23권5호
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• pp.36-43
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• 2014

광물찌꺼기에는 다양한 종류의 중금속이 함유되어 있어, 국내외에서 광물찌꺼기로부터 중금속을 제거하기 위해 많은 연구가 이루어졌으나, 중금속을 제거하기에는 여러 가지 문제점과 제약이 따르기 때문에 한계가 있었다. 따라서 이를 해결하고자 본 연구에서는 미립자의 선별까지도 가능한 다중비중선별기(Multi-gravity separator, MGS)를 사용하여 광물찌꺼기에 함유된 비소를 제거하기 위한 비중선별실험을 수행하였다. MGS를 이용하여 비중선별에 의해 비중이 높은 비소를 함유한 광물을 제거하고자 경사각, 세척수량, 광액농도, 드럼의 회전속도, 급광량에 따른 영향을 확인하였다. 실험결과 최적실험 조건인 MGS의 경사각 $3^{\circ}$, 세척수량 5 l/min., 광액농도 30%, 드럼 회전속도 208 rpm, 그리고 급광량 265.24 g/min. 에서 As 제거율과 산출율이 각각 88.21%와 92.25%인 결과를 얻었다.

• 대한금속재료학회지
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• 제49권2호
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• pp.174-179
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• 2011

We investigated the surface morphology changes of a lithium/sulfur battery using multi-walled canbon nanotube added sulfur electrode during charge-discharge cycling. The Li/S cell showed the first discharge capacity of 1286 mAh/g-S, which utilized is 71% of the theoretical value. It decreased to 328 mAh/g-S at the 100th cycle, which corresponds to about 19% utilization of the total sulfur in the cathode. The spherical lumps of the reaction product were observed on the surface of the sulfur electrode. This material was verified as lithium sulfide by X-ray diffraction measurement. The pores in the separator were filled with reaction product. Thus the diffusion of the $Li^+$ ion decreased, which resulted in the decreased capacity of the Li/S cell.

• 한국환경과학회지
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• 제26권8호
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• pp.955-966
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• 2017

Amendment of multi-binders was employed for the immobilization of metal(loid)s in field-contaminated soils to reduce the leaching potential. The effect of different types of multi-binders (lime/diammonium phosphate, diammonium phosphate/ladle slag and lime/ladle slag) on the solidification/stabilization of metal(loid)s (Pb, Zn, Cu and As) from the smelter soil and mine tailing soil were investigated. The amended soils were evaluated by measuring Toxicity Characterization Leaching Procedure (TCLP) leaching concentration of metal(loid)s. The results show that the leaching concentration of metal(loid)s decreased with the immobilization using multi-binders. In terms of TCLP extraction, the mixed binder was effective in the order of lime/ladle slag > diammonium phosphate/ladle slag > lime/diammonium phosphate. When the mixed binder amendment (0.15 g lime+0.15 g ladle slag for 1g smelter soil and 0.05 g lime+0.1 g ladle slag for 1 g mine tailing soil, respectively) was used, the leaching concentration of metal(loid)s decreased by 90%. However, As leaching concentration increased with diammonium phosphate/lime and diammonium phosphate/ladle slag amendment competitive anion exchange between arsenic ion and phosphate ion from diammonium phosphate. The Standard, Measurements and Testing programme (SM&T) analysis indicated that fraction 1 (F1, exchangeable fraction) decreased, while fraction 4 (F4, residual fraction) increased. The increased immobilization efficiency was attributed to the increase in the F4 of the SM&T extraction. From this work, it was possible to suggest that both arsenic and heavy metals can be simultaneously immobilized by the amendment of multi-binder such as lime/ladle slag.

• 한국추진공학회:학술대회논문집
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• 한국추진공학회 2011년도 제37회 추계학술대회논문집
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• pp.274-278
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• 2011

다양한 고에너지 물질이 포함된 폭발 장치를 정확하게 해석하기 위해서는 고에너지 물질의 다양한 연소 현상과 주변을 둘러싸고 있는 고체물질에 대한 대변형 현상을 정확하게 모사하는 것이 필수적이다. 이를 위하여 본 연구에서는 다중물질 각각의 경계면을 level set 함수를 이용하여 정확하게 표현하였으며, 경계면은 ghost fluid 기법을 사용하여 나타내었다. 각각의 물질에 대하여 대변형에 적합한 구성방정식을 사용하였으며, 지배방정식을 고차의 수치해석 기법을 사용하여 해석하였다. 다양한 폭발장치 중 실험적인 데이터를 이용하여 검증이 가능한 rate stick 문제를 해석하였으며, 실험과 유사한 결과를 획득하였다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제22권5호
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• pp.128-134
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• 2017

This work presents the adsorption capability of green tea and ginseng leaves to adsorb heavy metals such as Cd(II), Cu(II), and Pb(II) in aqueous solution. FT-IR analysis indicates the presence of oxygen containing functional groups (carboxyl groups) in two kinds of leaves. High pH condition was favorable to the adsorption of heavy metal ions due to the enhanced electrostatic attraction and the precipitation reaction of metal ions. The adsorption of Cd(II), Cu(II), and Pb(II) reached equilibrium within 10 min, achieving high removal efficiencies of 80.3-97.5%. The adsorption kinetics data of heavy metal ions were fitted well with the pseudo-second-order kinetic model. The maximum adsorption amounts of Cd(II), Cu(II), and Pb(II) ions were 8, 3.5, and 15 mg/g, respectively, in the initial concentration range from 0.15 to 0.75 mM. Based on the fitting data obtained from isotherm models, heavy metal adsorption by green tea and ginseng leaves could occur via multi-layer sorption.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2004년도 학술논문집
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• pp.337-337
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• 2004

As one of researches for the P ＆ T purposes, a basic experiment on the recovery of actinide elements from the mixture with rare earth elements by means of electrorefining using a liquid cadmium cathode in the LiCl-KC1 eutectic melt was carried out. In order to examine the behaviors of electrodeposition of metal ions on a liquid electrode, recovery experiments of rare earth metals resulting from forming electrodeposits were performed by a galvanostatic electrolysis method at various current densities. A cyclic voltammetric technique was applied to determine reduction-oxidation potential of each metal element in the melt and to detect the changes of the multi component melt composition for on-line monitoring. Also, a collaboration study with RIAR was completed to test the preliminary feasibility on a recovery of actinide elements from the mixture with rare earth elements using a liquid cadmium cathode and actinide metals. Experimental results showed that the ratio of actinides to rare earths, 9: 0.5∼1 led to the rare earth content of about 5∼10 wt% in the deposit.