• 자연과학논문집
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• 제8권1호
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• pp.61-69
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• 1995

$BaTiO_3$는 일반적으로 $BaCO_3$와 $TiO_2$의 고상반응으로 얻어지는데 BaO의 활성이 높고 이차상이 생성되므로 순수하게 합성하기가 어렵다. 순수한 $BaTiO_3$를 얻기 위해서 공침법, 가수분해법등이 연구되고 있으나 출발 원료가 비싸고 제조 공정상 문제로 고상반응으로 합성한 것과 별차이가 없다. 그래서 고상반응의 공정을 개선하는 연구가 다시 진행되고 있으며 본 연구에서도 $BaTiO_3$를 고상반응으로 합성할 때 물성에 좋지 않은 영향을 주는 이차상인 $Ba_2TiO_4$의 생성기구를 밝히고, 그것을 조절하려 했다. $BaTiO_3$의 이론조성중 Ba가 과잉인 영역에서는 $Ba_2TiO_4$가 $TiO_2$가 과잉인 영역에서는 $BaTiO_2O_5$와 $BaTiO_3O_7$이 소지의 팽창에 원인이 되었다. 환원에서 소결되는 $CeAIO_3$와 $BaTiO_3$계의 유전체는 공기중에서 $CeAIO_3$가 분해되고 이때 생성되는 $CeO_2$가 $BaTiO_3$의 전기적 물성에 큰 영향을 주었다.

• The Korean Journal of Ceramics
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• 제4권3호
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• pp.213-221
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• 1998

$BaCe_{0.9}Gd_{0.1_O_{2.95}$ powder was synthesized by oxalate coprecipitation method. Precipitate with a stoichimetric ratio of the cations was prepared by adding a mixture of Ba, Ce and Gd nitrate solution to an oxalic acid solution at pH 4. Reaction between the constituent oxides to form a perovskite phase was initiated at $800^{\circ}C$ and a single phase $BaCe_{0.9}Gd_{0.1_O_{2.95}$ powder having good sinterability was obtained after calcination at $1000^{\circ}C$. Sintering green compacts of this powder for 6 h showed a considerable densification to start at $1100^{\circ}C$ and resulted in 93% and 97% relative densities at $1300^{\circ}$ and at $1450^{\circ}C$, respectively. Whereas the power compacts prepared by solid state reaction had lower relative densities, 78% at $1300^{\circ}$and 90% at $1450^{\circ}C$. Fine particles of $CeO_2$ second phase were observed in the surface of the sintered compacts. This was attributed to the evaporation of BaO from the surface that had been exposed during thermal etching.

• 청정기술
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• 제29권4호
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• pp.313-320
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• 2023

대표적인 비암모니아성 선택적 촉매환원반응기인 H₂-SCR의 활용성을 높이기 위하여 Ce를 조촉매로 활용한 PtNi/CeO₂-W-TiO₂의 촉매 분말을 합성하고 다공성 금속 구조(porous metal structure, PMS)에 코팅하여 선택적 촉매 환원에 의한 NOx 제거 특성을 평가하였다. CeO₂를 조촉매로 사용한 H₂-SCR은 CeO₂를 사용하지 않은 경우에 비해 더 높은 NOx 제거 효율을 나타내었으며, CeO₂ 담지율 10 wt%에서는 반응온도 90℃에서 가장 높은 제거효율을 보였다. 한편, 촉매구조체인 PMS의 촉매 코팅량이 증가함에 따라 NOx 제거효율은 90℃ 이하에서는 향상되었으나, 120℃ 이상에서는 감소하는 경향을 보였고 공간속도를 4,000 h^-1에서 20,000 h^-1로 변경한 경우, 120℃이상의 온도에서 NOx 제거 효율이 향상되는 것을 확인할 수 있었다.

• 한국세라믹학회지
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• 제38권11호
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• pp.959-961
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• 2001

Nanosized CeO$_2$Powders were prepared under high temperature and pressure conditions by precipitation from metal nitrates with aqueous potassium hydroxide. Spherical shape of CeO$_2$powder was obtained at 175$^{\circ}C$ for 6h. TEM and X-ray diffraction patterns showed that the synthesized particle was crystalline. The average size and size distribution of the synthesized particles were below 30 nm and narrow, respectively. In addition, the effects of synthesis parameters under hydrothermal process are discussed.

• Progress in Superconductivity
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• 제12권1호
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• pp.6-11
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• 2010

The milling effects of a precursor $Y_2BaCuO_5$ (Y211) powder having 1 wt.% $CeO_2$ on the microstructure and critical current density ($J_c$) of liquid infiltration growth (LIG) processed $YBa_2Cu_3O_{7-y}$ (Y-123) bulk superconductors were investigated. The microstructure analysis revealed that the Y211 size in the final Y-123 products decreased with increasing the milling time and a relatively high density and uniform distribution of Y211 inclusions were observed in the sample prepared using 8 h milled powder. However, the unexpected Y211 particles coarsening was observed from the 4 h milled sample which was further increased for 10 h milled sample. Critical current density ($J_c$) of the LIG processed Y-123 bulk superconductors was found to be dependent on the milling time of the Y211 precursor powder. The $J_c$ increased with the increase of milling time and reached up to a maximum at 8 h in the self field while 10 h milled sample showed lower $J_c$ at the same field which might be due to the exaggerated growth and non-uniform distribution of Y211 particles.

• 한국세라믹학회지
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• 제42권12호
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• pp.808-815
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• 2005

[ $Bi_xCe_{l-x}O_{2-x/2}$ ](BD C : Bismuth Doped Ceria) powders with x = 0.1, 0.2, and 0.3 were synthesized using the Glycine Nitrate Process (GNP). They were then calcined at $500^{\circ}C$ for 2 hand sintered in a pellet or rod form at 900, 1000 or $1100^{\circ}C$ for 4 h for characterization as the alternative electrolyte material for intermediate temperature solid oxide fuel cells. The BDC powder consisted of a single phase of $CeO_2-Bi_2O_3$ solid solution in the as-synthesized state as well as in the as-calcined state with a mean powder size of 4.5nm in the former state and 6.5 - 10.1nm in the latter. On the contrary, the second phase of $\alpha-Bi_2O_3$ was observed to have been formed in the sinter with its amount increasing roughly with increasing temperature or $Bi_2O_3$ content. The BOC powder was superior in sinterability to other alternative electrolyte materials such as GDC, ScSZ, and LSGM with the minimum sintering temperature for a relative density of $95\%$ or larger as low as $1100^{\circ}C$. The ionic conductivity of BOC increased with $Bi_2O_3$ content and the maximum value of 0.119 S/cm was obtained at $800^{\circ}C$ for $Bi_{0.3}Ce_{0.7}O_{1.85}$.

• 한국원자력학회:학술대회논문집
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• 한국원자력학회 1998년도 추계학술발표회요약집
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• pp.267-267
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• 1998

• 한국세라믹학회지
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• 제44권3호
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• pp.182-187
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• 2007

10 mol% $Gd_{2}O_{3}-CeO_{2}$ powder was sintered by microwave in a 2.45 GHz multimode cavity to develop a dense electrolyte layer for intermediate temperature solid oxide fuel cells (IT-SOFCs). Samples were sintered from $1100^{\circ}C$ upto $1500^{\circ}C$ by $50^{\circ}C$ difference and kept for 10 min and 30 min at the maximum temperature respectively. Theoretical density of the sample sintered at $1200^{\circ}C$ for 10 min was 95.4% and increased gradually upto 99% in the sample sintered at $1500^{\circ}C$ for 30 min. All of sintered samples showed very fine microstructures and the maximum average grain size of the sintered sample at $1500^{\circ}C$ for 30 min was $(0.87{\pm}0.42){\mu}m$. Ionic conductvity of the samples were measured by DC 4 probe method.

• 한국분말재료학회지
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• 제12권6호
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• pp.413-421
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• 2005

Copper is able to work as a current collector under wide range of hydrocarbon fuels without coking in Solid oxide fuel cells (SOFCs). The application of copper in SOFC is limited due to its low melting point, which result in coarsening the copper particle. This work focuses on the sintering of copper powder with ceria coating layer. Ceria-coated powder was prepared by thermal decomposition of urea in $Ce(NO_3)_3\cdot6H_2O$ solution, which containing CuO core particles. The ceria-coated powder was characterized by XRD, ICP, and SEM. The thermal stability of the ceria-coated copper in fuel atmosphere $(H_2)$ was observed by SEM. It was found that the ceria coating layer could effectively hinder the grain growth of the copper particles.

• 한국세라믹학회지
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• 제38권9호
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• pp.794-798
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• 2001

Sol-gel법에 의하여 $Y_{2-x}SiO_5:Ce_x^{3+}$ (x=0.002∼0.04) 형광체를 제조하고 발광특성을 평가하였다. 800$^{\circ}$C에서 하소하였을 때는 무정형의 결정상이 나타났지만 1000$^{\circ}$C 이상에서는 $X_2$ type의 $Y_2SiO_5$ 결정상을 얻었다. 230∼360nm에서 형광체 모체의 광흡수가 일어났으며 300∼400nm에서 Ce 첨가로 인한 형광체의 광흡수가 관찰되었다. 436nm에서 최대의 발광 spectrum을 나타내었으며 $Ce^{3+}$ 함량을 0.025mol 첨가 시 $Y_{2-x}SiO_5:Ce_x^{3+}$ 형광체는 최대의 cathodoluminescence 특성과 CIE1931색 좌표 상에서 x=0.161, y=0.124의 색을 나타내었다.