• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2003년도 International Meeting on Information Display
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• pp.836-839
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• 2003

We have synthesized some phosphors in the system $CaO-Y_{2}O_3-Al_{2}O_{3}$ by combinatorial polymerized-complex method. Composition and synthetic temperature of phosphors in the liblary was screened from the emission intensities of individual samples under VUV excitation. In $Tb^{3+}$-activated $CaO-Y_{2}O_3-Al_{2}O_{3}$, green phosphors showing good intensity were found to be $CaYAl_{3}O_{7}$, $CaYalO_{4}$, $YAlO_{3}$, $Y_{3}Al_{5}O_{12}$, $Y_{4}Al_{2}O_{9}$, $Ca_{3}Al_{2}O6$.

• 한국세라믹학회지
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• 제31권6호
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• pp.629-636
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• 1994

The ferrimagnetic glass-ceramics in the system Fe2O3-CaO-SiO2 for hyperthermia were investigated. Glasses could be prepared up to the content of 40 wt% of Fe2O3 and below the weight ratio of 1.0 of CaO/SiO2. The maximum saturation magnetization and the maximum coercive force were 29.85 emu/g and 340.1 Oe respectively, for a glass 40Fe2O3.20CaO.40SiO2 composition heat-treated at 95$0^{\circ}C$ for 8 hours. And for a glass 40Fe2O3.30CaO.30SiO2 composition the maximum saturation magnetization and the maximum coercive force were 18.47 emu/g and 374.4 Oe heat-treated at 1,00$0^{\circ}C$ and 90$0^{\circ}C$ for 8 hours respectively. The maximum hysteresis loss was 1,726.3 cal/g for a glass 40Fe2O3.20CaO.40SiO2 composition heat-treated at 95$0^{\circ}C$ for 8 hours. It was found that the ferrimagnetic Fe2O3.CaO.SiO2 glass-ceramics was little injurious to human body as results of biocompatibility test and biotoxicity test.

• 마이크로전자및패키징학회지
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• 제6권2호
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• pp.75-81
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• 1999

$CaTiO_3$의 유전적 특성의 문제점을 해결하기 위해 $CaTiO_3$에 복합페로브스카이트 구조를 갖는$ La(Mg_{2/3}Ta_{1/3})O_3$를 고용시켜 마이크로파 유전특성을 조사하였다. XRD분석을 통하여 $CaTiO_3$에 $ La(Mg_{2/3}Ta_{1/3})O_3$를 첨가하면 고용체가 형성되며, 구조적으로는 Orthorhombic구조에서 $ La(Mg_{2/3}Ta_{1/3})O_3$의 첨가량이 증가함에 따라 단사정 대칭의 고용체형으로 바뀌어 가는 것을 확인할 수 있었다. (1-x)$CaTiO_3+xLa(Mg_{2/3}Ta_{1/3})O_3$에서 x값이 0.3일 때 유전율 49, 온도계수+$14ppm/^{\circ}C$, $Q \times f_0$ 값은 17000인 재료를 제조할 수 있었다.

• Bulletin of the Korean Chemical Society
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• 제18권8호
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• pp.831-840
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• 1997

Core/shell structured composite metal oxides of Fe2O3/MgO were prepared by thermal decomposition of Fe(acac)3 adsorbed on the surface of MgO cores. The morphology of the composites conformed to that of the MgO used as the cores. Broad powder X-ray diffraction peaks shifted toward larger d, large BET surface area (∼350 m2/g), and the size of crystalline domains in nano range (4 nm), all corroborate to the nanocrystallinity of the Fe2O3/MgO composite which was prepared by using nanocrystalline MgO as the core. By use of microcrystalline MgO as the core, microcrystalline Fe2O3/MgO composite was prepared, and it had small BET surface area of less than 35 m2/g. AFM measurements on nanocrystalline Fe2O3/MgO showed a collection of spherical aggregates (∼80 nm dia) with a very rough surface. On the contrary, microcrystalline Fe2O3/MgO was a collection of plate-like flat crystallites with a smooth surface. The nitrogen adsorption-desorption behavior indicated that microcrystalline Fe2O3/MgO was nonporous, whereas nanocrystalline Fe2O3/MgO was mesoporous. Bimodal distribution of the pore size became unimodal as the layer of Fe2O3 was applied to nanocrystalline MgO. The macropores in a wide distribution which the nanocrystalline MgO had were absent in the nanocrystalline Fe2O3/MgO. The decomposition of CCl4 was largily enhanced by the overlayer of Fe2O3 on nanocrystalline MgO making the reaction between nanocrystalline Fe2O3/MgO and CCl4 be nearly stoichiometric. The reaction products were environmentally benign MgCl2 and CO2. Such an enhancement was not attainable with the microcrystalline samples. Even for the nanocrystalline MgO, the enhancement was not attained, if not with the Fe2O3 layer. Without the layer of Fe2O3, it was observed that the nanocrystalline domain of the MgO transformed into microcrystalline one as the decomposition of CCl4 proceeded on its surface. It appeared that the layer of Fe2O3 on the particles of nanocrystalline Fe2O3/MgO blocked the transformation of the nanocrystalline domain into microcrystalline one. Therefore, in order to attain stoichiometric reaction between CCl4 and Fe2O3/MgO core/shell structured composite metal oxide, the morphology of the core MgO has to be nanocrystalline, and also the nanocrystalline domains has to be sustained until the core was exhausted into MgCl2.

• 한국결정성장학회지
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• 제14권3호
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• pp.123-128
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• 2004

융제(flux)로서 $B_2O_3$의 농도를 0-10 wt%까지 변화시킨 $SrAl_2O_4$ : $Eu^{+2}$, $Dy^{+3}$계 장잔광 형광체를 고상반응법으로 합성한 후, $B_2O_3$의 첨가량에 따른 결정특성과 장잔광 축광재료로서 가장 중요한 발광 및 장잔광 특성을 조사하였다. $SrAl_2O_4$ : Eu$^{+2}$, $Dy^{+3}$계 형광체는 $B_2O_3$의 농도에 관계없이 520nm 파장을 최대 발광파장으로 하는 발광스펙트럼을 나타내었고, 3wt%의 $B_2O_3$ 농도에서 최대 발광강도를 나타내었다. 그리고 $SrAl_2O_4$ : Eu$^{+2}$, $Dy^{+3}$ 형광체의 잔광강도 역시 $B_2O_3$의 농도에 무관하게 시간에 따라 모든 시료에서 지수 함수적으로 감소하였으나, $B_2O_3$의 농도가 3wt%인 경우에 발광의 감쇠속도가 작은 뛰어난 장잔광특성을 나타내었다.

• 대한전기학회:학술대회논문집
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• 대한전기학회 2007년도 Techno-Fair 및 추계학술대회 논문집 전기물성,응용부문
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• pp.114-115
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• 2007

In this study, low temperature sintering property of the $0.6TiTe_3O_8-0.4MgTiO_3$ ceramics with sintering adds were investigated for LTCC application which enable to cofiring with Ag electrode. $TiTe_3O_8$ mixed with $MgTiO_3$ to improve the temperature property. In the X-ray diffraction patterns, the columbite structure of $TiTe_3O_3$ phase and ilmenite structure of $MgTiO_3$ phase were coexisted in all specimens. In the case of $H_3BO_3$ addition, the bulk density and dielectric constant were decreased but quality factor was increased with amount of $H_3BO_3$ additions. The TCRF of the $0.6TiTe_3O_8-0.4MgTiO_3+xwt%H_3BO_3$ ceramics were moved to positive direction. In another case, SnO addition, the bulk density and dielectric constant were increased but Quality factor was decreased with amount of SnO additions. The TCRF of the $0.6TiTe_3O_8-0.4MgTiO_3$+ywt%SnO ceramics were shifted to negative direction. The dielectric constant, quality factor and TCRF of the $0.6TiTe_3O_8-0.4MgTiO_3$ ceramics with $2wt%H_3BO_3$ and 2.5wt%SnO sintered at $830^{\circ}C$ for 1h, were 28.5, 39,570GHz, $+9.34ppm/^{\circ}C$ and 29.86, 35,80000z, $-0.58ppm/^{\circ}C$, respectively.

• 한국세라믹학회:학술대회논문집
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• 한국세라믹학회 2002년도 추계총회 및 연구발표회 초록집
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• pp.30.1-30
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• 2002

• 한국세라믹학회:학술대회논문집
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• 한국세라믹학회 2003년도 추계총회 및 연구발표회 초록집
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• pp.144.1-144
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• 2003

• 한국세라믹학회지
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• 제32권2호
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• pp.234-238
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• 1995

MgFe2O4 formation, grain growth in Fe2O3, Fe solid-solution limit in MgO for MgO-Fe2O3 mixture were studied by means of investigating the distribution of phases and compositions in reaction area between MgO and Fe2O3. The reaction area at equlibrium was composed with MgO-FexO matrix and MgFe2O4 precipitation, MgFe2O4 was formed by precipitating from MgO-FexO matrix dependent on oxygen partial pressure. Fe contents was exponentially decreased with diffusion distance in MgO single crystal, and thus Fe solid-solution limitation in MgO was about 4mol%. The grain growth rate in Fe2O3 base was increased with Mg contents diffused from MgO single crystal.

• 한국세라믹학회지
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• 제38권10호
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• pp.936-941
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• 2001

5.31 mol% ${Y_2}{O_3}$-4.45 mo1% ${Nb_2}{O_5}$-90.31 mo1% $ZrO_2$에 ${Al_2}{O_3}$를 첨가한 복합체를 제조하여 알루미나 입도가 복합체의 균열 전파 저항성에 미치는 영향을 조사하였다. $ZrO_2/{Al_2}{O_3}$ 복합체에서는 R-cuve 거동이 관찰되었으며 0.2, $2.8{\mu}m$ ${Al_2}{O_3}$가 20 vol%가 첨가된 복합체의 인성값은 각각 7.9, $8.8MPam^{1/2}$이었다. 파괴인성값의 차이는 ${Al_2}{O_3}$ 입도 크기에 의존하는 $ZrO_2/{Al_2}{O_3}$ 복합체 내의 정방정 $ZrO_2$의 결정립 크기 차이에 의한 것으로 추정된다.