• Journal of the Korean Ceramic Society
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• v.40 no.11
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• pp.1120-1126
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• 2003

Yttrium Aluminum Garnet (YAG) powders were prepared by precipitation of Y hydroxides during milling of alumina powders. The powder calcined at 1200$^{\circ}C$ for 4 h contained a small amount of Yttrium Aluminum Monoclinic (YAM) in addition to YAG. However, phase-pure YAG was obtained in the compact of the milled powder with an average particle size of 0.57 ${\mu}$m at 1300$^{\circ}C$, which is much lower than those (l500∼1600$^{\circ}C$) for a mixed oxide method. The powder was found to exhibit an excellent sinterability regardless of the addition of a sintering aid, SiO$_2$(350 ppm Si). The undoped sample were sintered to a relative density of 98% at l600$^{\circ}C$. In contrast, the addition of SiO$_2$ caused a considerable densification to occur at 1500$^{\circ}C$ and the relative density reached 97.7%. But the sintering aid had little effect on the densification at 1600$^{\circ}C$, showing a similar relative density to the undoped sample.

• Journal of the Korean Vacuum Society
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• v.20 no.4
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• pp.294-299
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• 2011

In this study, single-walled carbon nanotubes (SWCNTs) were synthesized on a Fe/$Al_2O_3$/Si layer by thermal chemical vapor deposition. Metallic SWCNTs were selectively removed by microwave irradiation. Electrical and structural characterizations of the SWCNTs clearly revealed that the metallic SWCNTs were almost removed by microwave irradiation for 120 sec. The remained semiconducting SWCNTs with a high crystalline structure were obtained over 95%. This method would provide useful information for applications to SWCNTs-based field effect transistors and multifaceted nanoelectronics.

• The Journal of the Convergence on Culture Technology
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• v.9 no.3
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• pp.593-599
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• 2023

Nickel oxide (NiO) nanoparticles were successfully synthesized by a simple liquid phase process for producing ceramics powder using a precursor impregnated with a nickel(II) nitrate hexahydrate aqueous solution in an industrial pulp. The microfibrile structure of the precursor impregnated with nickel nitrate hexahydrate aqueous solution was confirmed by scanning electron microscope (SEM), and the crystal structure and particle size of nickel oxide (NiO) particles produced as the heat treatment temperature of the precursor were analyzed by X-ray diffraction (XRD) and SEM. As a result, it was confirmed through XRD and SEM analysis that the temperature at which the organic material of the precursor is completely thermally decomposed was 495-500℃, and the size and crystallinity of the nickel oxide particles produced increased as the heat treatment temperature increased. The size of the nickel oxide particles obtained by heat treatment at 500-800℃ for 1 hour was 50-200 nm. It was confirmed by XRD and SEM analysis that a NiO crystal phase was formed at a heat treatment temperature of 380℃, only a single NiO phase existed until 800℃.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.8 no.1
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• pp.42-48
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• 1998

Synthesis of PLT($Pb_{1-X}La_{2X/3}TiO_3$, x=0.1~0.3) powders was carried out by hydrothermal method. Optimal conditions for synthesis were $250^{\circ}C$ of reaction temperature, 8M-KOH solution of hydrothermal solvent and 12 hrs reaction time, and the monolithic $Pb_{1-X}La_{2X/3}TiO_3$ particles were obtained with the composition of x$\leq$0.2. The tetragonality(c/a) and the phase transition temperature were decreased by the increment of the $La_2O_3$ contents in PLT solid solutions, and the Curie temperature of the $Pb_{1-X}La_{2X/3}TiO_3$(x=0.2) was $400^{\circ}C$. The shape of the synthesized particles were nearly spherical and the size was in the 20~200 nm range.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.29 no.5
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• pp.203-207
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• 2019

Calcium phosphates such as hydroxyapatite (HAp), tricalcium phosphate (${\beta}$-TCP), and biphasic calcium phosphate (BCP, HAp/${\beta}$-TCP) have been prepared via hydrothermal treatment. The synthesis was conducted by reacting ($Ca(OH)_2$) aqueous solution with phosphoric acid ($H_3PO_4$) under different hydrothermal synthesis conditions (temperatures up to $150^{\circ}C$ and pH lower than 12). The effects of initial precursor Ca/P ratio (1.30, 1.50 and 1.67) and post heat treatment on the phase evolution behavior of the powders and sintered ceramics were investigated. The phases of resulting powders and sintered ceramics were controllable by adjusting the initial Ca/P ratio. A single HAp phase without any noticeable second phase was obtained for the initial Ca/P ratio of 1.67 in the overall heat treatment range. Pure ${\beta}$-TCP and biphasic calcium phosphate (HAp/${\beta}$-TCP) were synthesized from precursor solutions having Ca/P molar ratios of 1.30 and 1.50, respectively, after having been heat treated at $900^{\circ}C$ or higher. Dense ceramics with translucency were obtained at considerably lower sintering temperatures.

• Journal of the Korean Ceramic Society
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• v.36 no.1
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• pp.82-88
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• 1999

In this study, the formation of mullite phase with mineralizer have been investiagated Hadong Kaolin and boehmite were used as starting materials and also of TiCl4 and MnCl4 aquous solution were used as a mineralizer. In the addition of 3.5% MnO as a mineralizer, mullite single phase could be obtained at 125$0^{\circ}C$ without any other second phases. However in the addition of TiO2 as a mineralizer, mullite single phase is obtained at above 135$0^{\circ}C$. Therefore the formation of mullite is lowered in the case of MnO as a mineralizer than of TiO2. Because it is easy to obtain mullite single phase in the case of MnO addition, all the characteristics improved. The values of bulk density, water absorption and bending strength at room temperature were 2.72g/㎤, 0.27% and 180 MPa, respectively.

• Journal of the Korean Crystal Growth and Crystal Technology
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• v.31 no.2
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• pp.78-83
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• 2021

In this study, we prepared NiCo2O4 nanoparticles with large surface area by hydrothermal synthesis. In order to optimize the processing conditions for spinel NiCo2O4 nanoparticles with large surface area, experimental variables including concentration of Ni and Co precursor, reaction time, and temperature for post-heat treatment were evaluated. Optimized conditions for spinel NiCo2O4 with large surface area were [Ni]/[Co] 1:2 ratio, reaction time for 12 h, and post-heat treatment at 400℃. To investigate the feasibility as potential application for glucose sensor, electrochemical tests of the prepared NiCo2O4 nanoparticles in response to glucose was performed, which suggests that the NiCo2O4 can be suitable for a non-enzymatic-based electrochemical glucose sensor based on its high sensitivity and selectivity for glucose detection.

• Journal of the Korean Ceramic Society
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• v.38 no.2
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• pp.143-151
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• 2001

Ca/LiCl-KCl/CaCrO$_4$열 전지계의 양극재료로서 BCT(Body-Centered Tetragonal) 결정구조를 갖는 CaCrO$_4$분말을 GNP로 합성하고, SEM, TEM, XRD를 이용하여 그 미세구조를 분석하였다. GNP 공정에 의한 CaCrO$_4$분말은 단일상으로 0.5$mu extrm{m}$ 이하의 입자 크기를 가지며 균일하게 분포한 반면, 기존의 분말 혼합법은 높은 하수 온도 및 장시간의 하소 조건을 필요하므로 미세한 분말 합성이 어렵고 pellet 형태로 만들었을 때 GNP 분말에 비해 비표면적이 현저하게 작기 때문에 전극 재료로써 유리하지 못하다. Ca/LiCl-KCl/CaCrO$_4$계의 전기 화학적인 특성을 평가해본 결과 전지셀을 Ca/DEB(LiCl-KCl+CaCrO$_4$+SiO$_2$)와 같은 DEB 형태로 만들었을 때 $600^{\circ}C$의 온도에서 2.0 V이상 (<100 mA/㎤)의 안정한 전압이 5분 이상 유지되었다. 그러나 3층 전극 셀(Ca/LiCl/KCl/ CaCrO$_4$)에서는 동일한 온도에서 2.0 V이상 (<100 mA/㎤)의 전압이 7분 이상 유지되었으나 불안정한 전압 변동 및 낮은 peak voltage로 인해 DEB 셀의 전지 특성이 더 우수한 것으로 생각된다. 양극 재료의 제조 방법의 관점에서 볼 때, 동일한 DEB(Depolarizer : Electrolyte : Binder=25 : 70 : 5 wt%) 조성의 셀 구성시, GNP 분말은 분말 혼합법에 의한 분말보다 반응 표면적이 훨씬 크기 때문에 GNP 양극 활 물질의 DEB 셀에서의 전지 수명이 더 길었다.

• The Journal of Natural Sciences
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• v.15 no.1
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• pp.35-46
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• 2005

$LaFeO_3$ and substituted $LaFeO_3$ mixed oxides were prepared by Citrate and Cyanide method in air $850^{\circ}C$/24h. These oxides of orthorhombic perovskite were characterized by XRD and IR, but substituted $LaFeO_3$ with 0.5mol Cu at B site was not obtained single phase. Also, reduction reaction of un-substituted $LaFeO_3.17$ were two steps but each site substituted oxides were three steps reactions. These means that new reduction step of each site substituted oxides were atributed tot dopant.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2007.11a
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• pp.257-257
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• 2007

압전 액츄에이터의 효율적 작동을 위해서는 변위량이 크고 이력이 없으며 응답이 빠르고 온도특성이 좋아야 하는 등의 여러 조건들을 만족시켜야 한다. 따라서 본 실험은 압전 효율은 높이고 압전 손실은 낮추기 위하여 Pb$[(Mn_{1/3}Sb_{2/3})_{0.04}\;Zr_x\;Ti_y]O_3$, 세라믹스를 선정하였으며 Zr/Ti의 변화(x=0.47~0.5, y=0.46~0.49)에 따른 각각의 압전 특성 및 강유전 특성을 조사하였다. 일반적인 산화물 합성법을 이용하여 압전 분말을 제조하였고 EMAS standard(6001)에 근거하여 시편을 제조하였다. XRD 관찰결과 모든 조성에서 perovskite구조의 단일상만을 나타내는 소결체를 얻을 수 있었으며 FE-SEM 관찰결과 $1250^{\circ}C$의 소결시편이 $2-3{\mu}m$의 grain size를 갖는 치밀한 미세구조를 나타내었다. 가장 우수한 압전특성을 나타내는 조성은 Zr/Ti의 비가 0.485/0.475 조성이었으며 그때의 전기기계 결합계수(Kp) 값은 62.5%였고, 기계적 품질계수(Qm) 값은 1004였다.