• 한국진공학회지
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• 제10권1호
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• pp.119-126
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• 2001

ECR-PECVD 방법으로 ECR 플라즈마 소스 power, $CH_4/H_2$ 가스 혼합비와 유량, 증착시간 및 기판 bias 전압을 변화시켜 가면서 수소가 함유된 비정질 탄소 박막을 증착하고, 증착조건에 따라서 박막 내부에 함유되어 있는 수소함량 변화를 2.5 MeV 헬륨 이온빔을 사용하는 ERDa로 측정하였다. ERDA의 결과와 hES 및 RBS에 의한 성분분석으로부터 본 실첨에서 증착된 박막은 탄소와 수소만으로 구성 되어있음을 확인할 수 있었고, FTIR의 결과로부터 박막 증착조건에 따라서 박막 내부에 함유되어 있는 수소함량이 변화함을 알 수 있었다. 기판 bias 전압을 증가시킬수록 이온충돌 현상이 두드러져 탄소와 결합하고 있던 수소원자들이 떨어져 나가는 탈수소화 현상으로 수소함량이 크게 감소됨을 알 수 있었다. 그 밖의 조건에서는 박막증착 초기에는 수소보다 탄소량이 좀 더 많다가 점차적으로 수소함량이 증가되었고, 이때 박막 내부에 함유되어 있는 수소함량은 45~55% 범위 내에 있음을 확인할 수 있었다.

• 한국재료학회지
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• 제19권10호
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• pp.517-521
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• 2009

Si-C composite with hollow spherical structure was synthesized using ultrasonic treatment of organosilica powder formed by hydrolysis of phenyltrimethoxysilane. The prepared powder was pyrolyzed at various temperatures ranging from 900 to 1300 $^{\circ}C$ under nitrogen atmosphere to obtain optimum conditions for Li-ion battery anode materials with high capacity and cyclability. The XRD and elemental analysis results show that the pyrolyzed Si/C composite at 1100 $^{\circ}C$ has low oxygen and nitrogen levels, which is desirable for increasing the electrochemical capacity and reducing the irreversible capacity of the first discharge. The solid Si-C composite electrode shows a first charge capacity of $\sim$500 mAhg$^{-1}$ and a capacity fade within 30 cycles of 0.93% per cycle. On the other hand, the electrochemical performance of the hollow Si-C composite electrode exhibits a reversible charge capacity of $\sim$540 mAhg$^{-1}$ with an excellent capacity retention of capacity loss 0.43% per cycle up to 30 cycles. The improved electrochemical properties are attributed to facile diffusion of Li ions into the hollow shell with nanoscale thickness. In addition, the empty core space provides a buffer zone to relieve the mechanical stresses incurred during Li insertion.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2006년도 추계학술대회
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• pp.50-53
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• 2006

Regional geophysical surveys and geological cal studies on natural gas hydrate (NGH) in the East Sea were carried out by the Korea Institute of Geoscience and Mineral Resources (KIGAM) from 2000 to 2004. 16 piston cores, 2270 L-km of multi-channel reflection seismic (MCRS) data and 730 L-km of 3.5kHz Chirp data obtained from the southwestern part of the deep-water Ulleung Basin were analyzed in this study. In piston cores, cracks generally developed parallel to bedding suggest significant gas content. The core analyses showed high total organic carbon (TOC) content, sedimentation rate and heat flow of sediments. These are in favor of the general ion of substantial biogenic methane, which can form the NGH within the stability zone of the near seafloor sediments in the study area. The cores generally show also high residual hydrocarbon gas concentrations for the formation of natural gas hydrates The geophysical indicators of the presence of gas and/or NGH such as bottom simulating reflectors (BSRs), seismic blank Bones, pockmarks and gas seeping features were well defined on the MCRS and Chirp data.

• Bulletin of the Korean Chemical Society
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• 제34권12호
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• pp.3835-3839
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• 2013

A new synthesis route for Pt nanoparticles by direct electrochemical reduction of a solid-state Pt ion precursor ($K_2PtCl_6$) is demonstrated. Solid $K_2PtCl_6$-supported polyethyleneimine (PEI) coatings on the surface of glassy carbon electrode were prepared by simple mixing of solid $K_2PtCl_6$ into a 1.0% PEI solution. The potential cycling or a constant potential in a PBS (pH 7.4) medium were applied to reduce the solid $K_2PtCl_6$ precursor. The reduction of Pt(IV) began at around -0.2 V and the reduction potential was ca. -0.4 V. A steady state current was achieved after 10 potential cycling scans, indicating that continuous formation of Pt nanoparticles by electrochemical reduction occurred for up to 10 cycles. After applying the reduction potential of -0.6 V for 300 s, Pt nanoparticles with diameters ranging from $0.02-0.5{\mu}m$ were observed, with an even distribution over the entire glassy carbon electrode surface. Characteristics of the Pt nanoparticles, including their performance in electrochemical reduction of $H_2O_2$ are examined. A distinct reduction peak observed at about -0.20 V was due to the electrocatalytic reduction of $H_2O_2$ by Pt nanoparticles. From the calibration plot, the linear range for $H_2O_2$ detection was 0.1-2.0 mM and the detection limit for $H_2O_2$ was found to be 0.05 mM.

• 한국수소및신에너지학회논문집
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• 제26권4호
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• pp.324-330
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• 2015

The electrolyte flow rates of vanadium redox flow battery play very important role in terms of ion transfer to electrolyte, kinetics and pump efficiency in system. In this paper a vanadium redox flow battery single cell was tested to suggest the optimization criteria of electrolyte flow rates on the efficiencies. The compared electrolyte circulation flow rates in this experimental work were 15, 30 and 45 mL/min. The charge/discharge characteristics of the flow rate of 30 mL/min was the best out of all flow rates in terms of charging and discharging time. The current efficiencies, voltage efficiencies and energy efficiencies at the flow rate of 30 mL/min were the best. The IR losses obtained at thd current density of $40mA/cm^2$, at the flow rates of 15, 30 and 45 mL/min were 0.085 V, 0.042 V and 0.115 V, respectively. The charge efficiencies at the current density of $40mA/cm^2$ were 96.42%, 96.45% and 96.29% for the electrolyte flow rates of 15, 30 and 45 mL/min, respectively. The voltge efficiencies at the current density of $40mA/cm^2$ were 77.34%, 80.62% and 76.10% for the electrolyte flow rates of 15, 30 and 45 mL/min, respectively. Finally, the energy efficiencies at the current density of $40mA/cm^2$ were 74.57%, 77.76% and 73.27% for the electrolyte flow rates of 15, 30 and 45 mL/min, respectively. The optimum flow rates of electrolytes were 20 mL/min in most of operating variables of vanadium redox flow battery.

• Korean Chemical Engineering Research
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• 제49권1호
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• pp.10-14
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• 2011

철 이온 교환방법에 의해 메조기공을 갖는 활성탄소 섬유(ACF)를 제조하고, 이를 사용하여 전기 이중층 커패시터(EDLC)의 전극소재 성능을 조사하였다. 질산처리에 의해 제조된 메조기공 ACF는 비표면적이 1,249, 664 $m^2/g$이고, 메조 기공 분율이 70.6-81.3%이고, 평균 기공크기는 약 2.78~4.14 nm이다. 질산처리시간이 짧을수록 비표면적이 크고 메조 기공이 적게 발달됨을 알 수 있었다. 전기이중층 커패시터의 성능을 조사하기 위해서, 메조기공 ACF, 도전제, 바인더를 사용하여 단위 셀을 제조하였으며, 유기 전해질을 사용하였다. 2시간 질산으로 처리된 ACF의 비 축전양은 0.47 $F/cm^2$이고, 20회 충.방전 테스트에서 안정된 실험결과를 얻을 수 있었다. EDLC의 전기화학적 성능은 ACF 전극의 비표면적에 크게 영향을 받으며 메조기공은 전하의 확산저항을 감소시키는 것을 알 수 있었다.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2005년도 Proceedings of The 6th korea-china joint workshop on nuclear waste management
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• pp.165-175
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• 2005

Measurement of spent resin activity was initiated in 2004 in order to develop the C-14 removal technology for safe disposal. As part of this program, spent resins were sampled and measured in the in-station resin storage tank 2 at Wolsong Nuclear Power Plant Unit 1. At the time of sampling, the resins had been in storage tank from 3 to 23 years. Total 72 resin samples were sampled, which were collected from both man-hole (68 samples) and test-hole (4 samples) in the in-station resin storage tank 2. They were separated into liquid, activated carbon, zeolite, and spent resin. The spent resins were oxidized with sample oxidizer and analyzed for C-14. Ten of collected mixed resin samples were separated by density into cation and anion resins using a sugar solution. The C-14 concentration in anion exchange resin was approximately 2 times higher than in the mixed resin. The average concentration of C-14 in the cation/anion mixed exchange resin was $460\;GBq/m^3$ from test-hole and $53.1\;GBq/m^3$ from man-hole. We have found that concentration of C-14 in the spent resin is about from 0.4 to $1,321\;GBq/m^3$. So it could be a problem, when dispose of at a repository, since there is a disposal limit of $222\;GBq/m^3$. This means we should develop the C-14 removal technology.

• 멤브레인
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• 제24권4호
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• pp.332-339
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• 2014

본 연구에서는 축전식 탈이온 공정(capacitive deionization, CDI)의 성능을 개선하기 위해 poly(2,6-dimethyl-1,4-phenylene oxide) (PPO)를 기저물질로 이용하여 코팅이 가능한 음이온교환 이오노머(quaternized PPO, QPPO) 용액을 제조하였다. 제조된 QPPO는 상용 음이온교환막(AMX, Astom Corp., Japan) 대비 우수한 이온전도도 특성을 나타내었으며 전기화학적 특성 또한 동등 수준임을 확인할 수 있었다. 다공성 탄소 전극에 이오노머 용액을 코팅하여 CDI 성능평가를 수행하였으며 그 결과 약 94.9%의 높은 염 제거 효율을 나타내었다. 기존의 CDI와 상용 음이온교환막을 결합한 membrane CDI (MCDI), QPPO가 코팅된 전극을 사용한 coated CDI (CCDI)의 탈염 성능을 비교한 결과 QPPO의 높은 이온선택성 및 낮은 이온 전달저항으로 CCDI가 기존의 CDI에 비해 52.1%, MCDI에 비해 18.3% 향상된 높은 염 제거 성능을 나타냄을 확인하였다.

• 한국재료학회지
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• 제5권8호
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• pp.960-965
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• 1995

반응 가스 분압의 조절에 의한 HCD식 이온 도금 법으로 다양한 조성의 Ti(C, N) 경질 피막을 ASP30 공구강에 도금하였고 이 피막의 내마모성에 대한 조성의 영향을 경도, 밀착력 및 마모기구의 변화 등의 관점에서 고찰하였다. 경도는 질소나 탄소와 같은 비금속 성분량의 증가에 비례하지만 탄소함유량의 중가는 밀착력을 오히려 감소시켰다. 이 경향은 피막 밀도가 비교적 작은 정략적비 이하인 구간([C+N]/Ti<1)에서 보다 그 이상인 조성에서 영향이 뚜렷하였다. 따라서 피막의 내마모 특성은 높은 경도를 유지할 수 있는 ([C+N]/Ti>1)인 구역 내에서 밀착력 저하에 의한 adhesive 형태로의 마모 기구 변이를 억제할 수 있는 저 탄소 조성을 가질 때 최대로 된다.

• 한국산업융합학회 논문집
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• 제7권1호
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• pp.107-113
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• 2004

Several transition metal complexes, [$M(L)X_2$](M=Pd(II), Ni(II); X=CI, Br) are prepared with aminophosphine ligands such as 1,2-bis{(diphenylphosphino)amino}ethane{$Ph_2PNHCH_2CH_2NHPPh_2$}($L_1$), 1,2-bis{(diphenylphosphino)amino}propane{$Ph_2PNHCH(CH_3)CH_2NHPPh_2$}($L_2$), trans-1,2-bis{(diphenylphosphino)amino}cyclohexane{$Ph_2PNHC_6H_{10}NHPPh_2$}($L_3$) and 1,2-bis{(diphenylphosphino)amino}benzene{$Ph_2PNHC_6H_4NHPPh_2$}($L_4$). The properties of these complexes are characterized by optical spectroscopic methods including UV/vis spectroscopy, CD, IR, $^1H$- and $^{31}P-NMR$ together with conductometer and elemental analysis. All complexes are stable under atmospheric environment. Catalytic reactivity for C-C coupling between [$M(L)X_2$] and Grignard reagents(RMgX; R=phenyl, propyl, buthyl) by thermolysis were investigated utilizing GC/mass, $^1H$- and $^{13}C-NMR$. When mol scale is 1:20 at [$Pd(L)Cl_2$] and Grignard reagents, the high catalytic activity for C-C coupling is apparent. The [$M(L)X_2$](X=Cl, Br) complexes which have strong bond at M-P exhibit high yields for C-C coupling reactions. When the central metal ion is Pd(II), the high catalytic activity for C-C coupling is apparent. The complex coordinated with Br shows higher catalytic activity for C-C coupling reactions compared to Cl.