• Bulletin of the Korean Chemical Society
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• 제35권8호
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• pp.2349-2356
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• 2014

The recycling technology by the catalytic conversion is one of the most promising techniques for the $CO_2$ treatment of coal burning power plant flue gases. The conversion of $CO_2$ to valuable product of $CH_4$ can be used as a fuel to run the turbine for electricity generation. Through this technique, the amount of coal needed for the combustion in a gas turbine can be reduced as well as $CO_2$ emissions. Therefore, a series of catalysts based on cerium oxide doped with copper, nickel and manganese were prepared by impregnation method. From the characterization analysis, it showed that the prepared catalysts calcined at $400^{\circ}C$ were amorphous in structure with small particle size in the range below 100 nm. Meanwhile, the catalyst particles were aggregated and agglomerated with higher surface area of $286.70m^2g^{-1}$. By increasing the calcination temperature of catalysts to $1000^{\circ}C$, the particle sizes were getting bigger (> 100 nm) and having moderate crystallinity with lower surface area ($67.90m^2g^{-1}$). From the catalytic testing among all the prepared catalysts, Mn/Ce-75/$Al_2O_3$ calcined at $400^{\circ}C$ was assigned as the most potential catalyst which gave 49.05% and 56.79% $CO_2$ conversion at reaction temperature of $100^{\circ}C$ and $200^{\circ}C$, respectively.

• 한국자기학회지
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• 제5권5호
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• pp.427-431
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• 1995

The influence of Nd and B contents on the magnetic properties and structures of ${\alpha}-Fe$ based Nd-(Fe,Co)-B-Mo-Cu alloys was investigated. $Nd_{4}{(Fe_{0.9}Co_{0.1})}_{92-x}B_{x}Mo_{3}Cu_{1}$ and $Nd_{x}{(Fe_{0.9}Co_{0.1})}_{86-x}B_{10}Mo_{3}Cu_{1}$ amorphous alloys prepared by rapid solidification process were crystallized to form nanocrystalline structure. The increase of B content in $Nd_{4}{(Fe_{0.9}Co_{0.1})}_{92-x}B_{x}Mo_{3}Cu_{1}$ nanocrystalline resulted in the change of stucture of soft phase in the sequence of ${\alpha}-Fe$->${\alpha}-Fe+Fe_{3}B$->$Fe_{3}B$. The coercivitis of the alloys were increased with increasing B content and was 263 kA/m at x=18. On the contrary, the remanence has shown an opposite trends. The increase of Nd content in $Nd_{x}{(Fe_{0.9}Co_{0.1})}_{86-x}B_{10}Mo_{3}Cu_{1}$ nanocrystalline containing ${\alpha}-Fe$ as main phase had no effect on the structure and improved coercivity up to 256 kA/m. However, the remanence was decreased from 1.4 T to 1.15 T according to the increase of Nd content.

• 한국분말재료학회지
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• 제13권5호
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• pp.351-359
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• 2006

Ni based($Ni_{57}Zr_{20}Ti_{18}Si_2Sn_3$) bulk metallic glass(BMG) powders were produced by a gas atomization process, and ductile Cu powders were mixed using a spray drying process. The Ni-based amorphous powder and Cu mixed Ni composite powders were compacted by a spark plasma sintering (SPS) processes into cylindrical shape. The relative density varied with the used SPS mold materials such as graphite, hardened steel and WC-Co hard metal. The relative density increased from 87% to 98% when the sintering temperature increased up to $460^{\circ}C$ in the WC-Co hard metal mold.

• 한국수소및신에너지학회논문집
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• 제17권4호
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• pp.448-453
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• 2006

Porous Co-P catalysts electroplated on Cu in chloride based solution with an addition of $NaH_2PO_2$ and glycine were developed for hydrogen generation from alkaline $NaBH_4$ solution. The microstructures of the Co-P catalysts and their hydrogen generation properties were analyzed as a function of cathodic current density and plating time during the electrodeposition. Amorphous Co-P electrodeposits with porous structure was formed on Cu at cathodic current density of $0.05\;A/cm^2$, and showed very high hydrogen generation rate in alkaline $NaBH_4$ solution due to an increase in the surface area of the catalyst as well as the catalytic activity. The Co-P catalyst, which was obtained at cathodic current density of $0.05\;A/cm^2$ for 5 min, exhibited the best hydrogen generation rate of 2290 ml/min.g-catalyst in 1 wt. % NaOH+10 wt. % $NaBH_4$ solution at $30^{\circ}C$.

• 폴리머
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• 제26권6호
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• pp.785-791
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• 2002

결정성 및 무정형 고분자 전해질의 이온전도 거동에 미치는 초임계 이산화탄소 (sc$CO_2$) 유체의 영향에 대해 조사하였다. 본 연구는 폴리에테르 전해질의 이온전도도 향상에 관한 새로운 개념의 접근 방법이다. sc$CO_2$ 처리결과, 결정성 PEO 전해질의 경우 실온에서 100배 이상의, 무정형 PMEO 전해질은 9$0^{\circ}C$에서 30배 가까운 이온전도도의 상승을 나타내었다. 이는 고분자 매트릭스 내부로 $CO_2$ 분자가 침투함으로써 이온 분산효과로 캐리어 이온의 수를 증가시키고 가소화 효과로 인해 유리전이온도를 저하시켜 이온이동도를 향상시킨 결과이다.

• 한국자기학회지
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• 제15권6호
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• pp.315-319
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• 2005

본 연구에서는 자기터널접합(MTJs; magnetic tunnel junctions)의 스위칭 자기장($H_{SW}$)을 감소시키기 위하여 자유층으로 비정질 강자성 $Co_{70.5}Fe_{4,5}Si_{15}B_{10}$ 단일(single) 및 합성형 반강자성(SAF; synthetic antiferromagnet) 층을 사용하였다. $Si/SiO_2/Ta$ 45/Ru 9.5/IrMn 10/CoFe 7/AlOx/CoFeSiB 7 or CoFeSiB (t)/Ru 1.0/CoFeSiB (7-t)/Ru 60 (in nm) MTJs의 자기저항과 스위칭 특성을 CoFe 자유층과 NiFe 자유층을 갖는 MTJs와 비교하여 조사하였다. CoFeSiB은 포화자화($M_s$)가 $560\;emu/cm^3$으로 CoFe보다 낮고, 이방성 상수(Ku)는 $2800 erg/cm^3$으로 NiFe보다 높다. CoFeSiB SAF 구조에서 CoFeSiB 사이의 Ru 두께가 1.0 nm일 때 교환결합에너지($J_{ex}$)는 $-0.003erg/cm^2$였다. 이와 같이 비교적 작은 $J_{ex}$ 때문에, CoFeSiB SAF 자유층을 갖는 MTJs의 실험 및 Landau-Lisfschitz-Gilbert(LLG)식에 의한 시뮬레이션 결과 모두에서 $H_{SW}$가 접합크기에 의존하는 경향을 보였다. CoFeSiB SAF 자유층 MTJ의 $H_{SW}$는 CoFe, NiFe 또는 CoFeSiB single을 자유층으로 하는 MTJs에 비해 훨씬 낮게 나타났다. 따라서 CoFeSiB SAF를 자유층으로 사용한 MTJ는 micrometer에서 submicrometer 크기 영역 모두에서 보지적의 감소와 민감도 증가와 같은 우수한 스위칭 특성을 갖는 것을 확인하였다.

• 대한전자공학회논문지SD
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• 제48권6호
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• pp.1-6
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• 2011

투명 산화물 반도체 (Transparent Oxide-TFT)를 활성층과 소스/드레인, 게이트 전극층으로 동시에 사용한 비결정 indium zinc oxide (a-IZO), 절연층으로 co-sputtered $HfO_2-Al_2O_3$ (HfAIO)을 적용하여 실온에서 RF-magnetron 스퍼터 공정에 의해 제작하였다. TFT의 게이트 절연막으로써 $HfO_2$ 는 그 높은 유전상수( > 20)에도 불구하고 미세결정구조와 작은 에너지 밴드갭 (5.31eV) 으로 부터 기인한 거친계면특성, 높은 누설전류의 단점을 가지고 있다. 본 연구에서는, 어떠한 추가적인 열처리 공정 없이 co-sputtering에 의해 $HfO_2$와 $Al_2O_3$를 동시에 증착함으로써 구조적, 전기적 특성이 TFT 의 절연막으로 더욱 적합하게 향상되어진 $HfO_2$ 박막의 변화를 x-ray diffraction (XRD), atomic force microscopy (AFM) and spectroscopic ellipsometer (SE)를 통해 분석하였다. XRD 분석은 기존 $HfO_2$ 의 미세결정 구조가 $Al_2O_3$와의 co-sputter에 의해 비결정 구조로 변한 것을 확인 시켜 주었고, AFM 분석을 통해 $HfO_2$ 의 표면 거칠기를 비교할 수 있는 RMS 값이 2.979 nm 인 것에 반해 HfAIO의 경우 0.490 nm로 향상된 것을 확인하였다. 또한 SE 분석을 통해 $HfO_2$ 의 에너지 밴드 갭 5.17 eV 이 HfAIO 의 에너지 밴드 갭 5.42 eV 로 향상 되어진 것을 알 수 있었다. 자유 전자 농도와 그에 따른 비저항도를 적절하게 조절한 활성층/전극층 으로써의 IZO 물질과 게이트 절연층으로써 co-sputtered HfAIO를 적용하여 제작한 Oxide-TFT 의 전기적 특성은 이동도 $10cm^2/V{\cdot}s$이상, 문턱전압 2 V 이하, 전류점멸비 $10^5$ 이상, 최대 전류량 2 mA 이상을 보여주었다.

• Applied Microscopy
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• 제45권2호
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• pp.37-43
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• 2015

In present work, work-hardening behavior of TiCu-based bulk metallic glass composite with B2 particles has been studied by systemic structural and mechanical investigations. After yield, pronounced work-hardening of the alloy was clearly exhibited, which was mainly related to the martensitic transformation as well as the deformation twinning in B2 particles during deformation. At the early plastic deformation stage (work-hardening stage), the stress-induced martensitic transformation from B2 phase to B19' phase and deformation-induced twinning of B19' phase was preferentially occurred in the around interface areas between B2 phase and amorphous matrix by stress concentration. The higher hardness value was observed in vicinity of interface within the B2 particles which are probably connected with martensitic transformation and deformation twinning. This reveals that the work-hardening phenomenon of this bulk metallic glass composite is a result of the hardening of B2 particles embedded in amorphous matrix.

• 한국자기학회지
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• 제12권1호
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• pp.30-33
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• 2002

초미세결정렵 Nd-Fe-B-Mo-Cu합금에서 Co 치환이 미세조직과 자기특성에 미치는 영향을 조사 하였다. 급속응고법으로 제조된 비정질 Nd-(Fe, Co)-B-Mo-Cu합금은 결정화에 의하여 $\alpha$-Fe기 초미세결정립 Nd-(Fe, Co)-B-Mo-Cu합금이 제조되었다. Co로의 Fe치환은 결정립 미세화에 기여하며, 이로 인하여 경자기특성이 개선되었다. 최적열처리된 초미세결정립 N $d_4$(F $e_{0.85}$ $Co_{0.15}$)$_{82}$ $B_{10}$M $o_3$Cul합금의 잔류자화, Curie온도는 Co가 치환되지 않은 합금에 비하여 개선된 우수한 특성을 나타내었다. 64$0^{\circ}C$, 10분 열처리된 초미세결정립 N $d_4$(F $e_{0.85}$ $Co_{0.15}$)$_{82}$ $B_{10}$M $o_3$Cu 합금의 평균결정립 크기는 약 15 nm이며, 이때 보자력, 잔류자화 및 최대에너지적은 각각 239kA/m, 1.4 T 및 103.5 kJ/ $m^3$이었다.

• Bulletin of the Korean Chemical Society
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• 제31권8호
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• pp.2304-2308
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• 2010

A $LiNi_{0.8}Co_{0.15}Al_{0.05}O_2$ (LNCAO/C) active material composite cathode was coated with carbon. The conductive carbon coating was obtained by addition of surfactant during synthesis. The addition of surfactant led to the formation of an amorphous carbon coating layer on the pristine LNCAO surface. The layer of carbon coating was clearly detected by FE-TEM analysis. In electrochemical performance, although the LNCAO/C showed similar capacity at low C-rate conditions, the rate capability was improved by the form of the carbon coating at high current discharge state. After 40 cycles of charge-discharge processes, the capacity retention of LNCAO/C was better than that of LNCAO. The carbon coating is effectively protected the surface structure of the pristine LNCAO during Li insertion-extraction.