• 제목/요약/키워드: O_3

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Fe_2O_3-CaO-SiO_2$계 결정화 유리의 제조 및 특성(I) (Characterization and Preparation of Glass-Ceramics in the System Fe_2O_3-CaO-SiO_2$ (I))

  • 이용근;최세영;김경남
    • 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.

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CaTiO$_3$-La(Mg$_{2}$3/Ta$_{1}$3/)O$_3$ 계의 고주파 유전특성 (Microwave Dielectric Characteristics of CaTiO$_3$-La(Mg$_{2}$3/Ta$_{1}$3/)O$_3$ System)

  • 박찬식;이경호;김경용
    • 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$$ 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.

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Effect of Core Morphology on the Decomposition of CCI₄ over the Surface of Core/Shell Structured Fe₂O₃/MgO Composite Metal Oxides

  • 김해진;강진;박동곤;권호진;Kenneth J. Klabunde
    • 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.

$SrAl_2O_4:Eu^{+2},\;Dy^{+3}$ 장잔광 형광체에 있어서 발광 및 장잔광특성에 미치는$B_2O_3$의 영향 (Effects of $ B_2O_3$ composition for the photoluminescence and after-glow charcteristics of $SrAl_2O_4:Eu^{+2},\;Dy^{+3}$ phosphors)

  • 이영기;엄기석
    • 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.

소결조제 첨가에 따른 $0.6TiTe_3O_8-0.4MgTiO_3$ 세라믹스의 jdhs 소결 특성 (Low Temperature Sintering Properties of the $0.6TiTe_3O_8-0.4MgTiO_3$ Ceramics with Sintering Adds)

  • 김재식;류기원;고중혁;이영희
    • 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.

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Fe$_2O_3/(Al_2O_3+Ga_2O_3)$ 변화에 따른 $(EuBi)_3(FeAlGa)_5O_{12},(EuTbBi)_3(FeAlGa)_5O_{12}$ 가네트 단결정 후막의 성장과 자기적 특성 (Growth and Magnetic Properties $(EuBi)_3(FeAlGa)_5O_{12},(EuTbBi)_3(FeAlGa)_5O_{12}$ Garnet Single Crystal Thick Films by $Fe_2O_3/(Al_2O_3+Ga_2O_3)$ Molar Ratio)

  • 김근영;윤석규;이성문;윤대호
    • 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
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단결정 MgO와 분말 $Fe_2O_3$간의 고상 반응 연구 (The Study on Solid-State Reaction Between MgO Single Crystal and $Fe_2O_3$ Powder)

  • 김성재;박재우
    • 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.

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알루미나 입도가 (Y,Nb)-TZP/${Al_2}{O_3}$ 복합체의 R-curve 거동에 미치는 영향 (Effect of Alumina Particle Size on R-curve Behavior of (Y,Nb)-TZP/${Al_2}{O_3}$ Composites)

  • 이득용;김대준;김배연;송요승
    • 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$${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.

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저온 소성용 SiO$_2$-TiO$_2$-Bi$_2$O$_3$-RO계(RO :BaO-CaO-SrO) Glass/ceramic 유전체 재료의 B$_2$O$_3$첨가에 따른 Ag 후막과의 동시 소결시 정합성 밀 유전 특성에 관한 연구 (A Study on the Co-firing Compatibility with Ag-thick film and Dielectric Characteristics of Low Temperature Sinterable SiO$_2$-TiO$_2$-Bi$_2$O$_3$-RO system (RO :BaO-CaO-SrO) Glass/Ceramic Dielectric Material with the Addition of B$_2$O$_3$)

  • 윤장석;이인규;유찬세;이우성;강남기
    • 마이크로전자및패키징학회지
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    • 제6권3호
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    • pp.37-43
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    • 1999
  • 고주파에서 사용하기 위한 $SiO_2-TiO_2-Bi_2O_3$-RO계(RO:BaO-CaO-SrO)를 주성분으로 하는 결정화 유리와 세라믹 충진재로서 $Al_2O_3$를 혼합하여 제조한 저온 소성용 Glass/Ceramic 유전체 모재와 Ag-thick film의 동시 소결시 발생할 수 있는 소결 부정합과 그 해소 방안을 연구하였다. 적층된 Glass/Ceramic 유전체 sheet와 Ag-thick film의 동시 소결시에 소결체는 sheet와 film의 densification rate 차 등에 의해 큰 camber 현상과 그로 인해 Ag-film에 crack이 발생하였다. 이를 교정하기 위해 유리 성분과 $Al_2O_3$성분이 혼합된 유전체 분말에 $B_2O_3$를 6, 8, 10, 12, 14 vol% 첨가한 결과를 보면 $B_2O_3$첨가량이 증가함에 따라 소결체의 camber 현상은 점점 크게 줄어들었으며 14 vol% 첨가된 경우에는 거의 관찰되지 않았다. 또한 $BaO_3$첨가량이 증가함에 따라 유전율($varepsilon_{r}$)은 점점 감소하였고 Q$\times$f 값은 크게 증가하는 경향을 나타내었으며 $\tau_{f}$ 값은 양(+)의 값으로 점점 크게 변하였다.

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