• 제목/요약/키워드: c-$Al_2O_3$

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Ba-페라이트/$SiO_2$ 자성박막에서 ${\alpha}-Al_2O_3$ buffer 층의 역할 (Role of ${\alpha}-Al_2O_3$ buffer layer in $Ba-ferrite/SiO$ magnetic thin films)

  • 조태식;정지욱;권호준
    • 한국전기전자재료학회:학술대회논문집
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    • 한국전기전자재료학회 2003년도 추계학술대회 논문집 Vol.16
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    • pp.267-270
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    • 2003
  • We have studied the interfacial diffusion phenomena and the role of ${\alpha}-Al_2O_3$ buffer layer as a diffusion barrier in the $Ba-ferrite/SiO_2$ magnetic thin films for high-density recording media. In the interface of amorphous Ba-ferrite ($1900-{\AA}-thick)/SiO_2$ thin film during annealing, the interfacial diffusion started to occur at ${\sim}700^{\circ}C$. As the annealing temperature increased up to $800^{\circ}C$, the interfacial diffusion abruptly proceeded resulting in the high interface roughness and the deterioration of the magnetic properties. In order to control the interfacial diffusion at the high temperature, we introduced ${\alpha}-Al_2O_3$ buffer layer ($110-{\AA}-thick$) in the interface of $Ba-ferrite/SiO_2$ thin film. During the annealing of $Ba-ferrite/{\alpha}-Al_2O_3/SiO_2$ thin film even at ${\sim}800^{\circ}C$, the interface was very smooth. The smooth interface of the film was also clearly shown by the cross-sectional FESEM. The magnetic properties, such as saturation magnetization 3nd intrinsic coercivity, were also enhanced, due to the inhibition of interfacial diffusion by the ${\alpha}-Al_2O_3$ buffer layer. Our study suggests that the ${\alpha}-Al_2O_3$ buffer layer act as a useful interfacial diffusion barrier in the $Ba-ferrite/SiO_2$ thin films.

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Fabrication and Strength Properties of LPS-SiC based materials

  • Lee, Sang-Pill;Kohyama, Akira
    • 한국해양공학회:학술대회논문집
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    • 한국해양공학회 2006년 창립20주년기념 정기학술대회 및 국제워크샵
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    • pp.25-28
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    • 2006
  • This paper dealt with the LPS process for the development of high performance SiC materials, based on the detailed analysis of their microstructure and mechanical properties. The submicron SiC powder was used for the fabrication of LPS-SiC materials. A mixture of $Al_2O_3$ and $Y_2O_3$ particles was also used as a sintering additive in the LPS process. LPS-SiC materials were fabricated at different temperatures, using various additive composition ratio ($Al_2O_3/Y_2O_3$). The total amount of additive materials ($Al_2O_3+Y_2O_3$) was fixed as 10 wt%. The characterization Of LPS-SiC materials was investigated by means of SEM, XRD and three point bending test. The LPS-SiC material represented a relative density of about 98 % and a flexural strength of about 800MPa, when it was fabricated at the temperature of $1820^{\circ}C$ and the additive compositional ratio of 1.5.

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크롬을 사용한 Tialite계 안료 (Cr-doped Tialite Pigments)

  • 김연주;이병하
    • 한국재료학회지
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    • 제21권9호
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    • pp.515-519
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    • 2011
  • The purpose of this study was to determine the optimal firing condition and composition for $Al_2TiO_5$ crystal, which is suitable for stable coloration in glazes at high temperatures, using $Cr_2O_3$ as chromophore for the synthesis of $Al_2TiO_5$ system pigments. $Al_2TiO_5$ has a high refractive index and good solubility of chromophore in the $Al_2TiO_5$ lattice, making this structure a good candidate for the development of new ceramic pigments. Pigments were synthesized by using $Al_2O_3$ and $TiO_2$ mainly. Various amounts of $Cr_2O_3$ such as 0.01, 0.02, 0.03, 0.04 and 0.05 mole were also added. Each compound was synthesized at $1300^{\circ}C$, $1400^{\circ}C$, and $1500^{\circ}C$ for 2 hours and cooled naturally. The crystal structure, solubility limit, and color of the synthesized pigments were analyzed by XRD, SEM, Raman spectroscopy, UV and UV-vis. The changes in color as the result of applying 6 wt% of the synthesized pigments to lime barium glaze were expressed as CIE-L*a*b* values. A $Cr_2O_3$ 0.03 mole doped $Al_2TiO_5$ brown pigment was successfully synthesize at $1400^{\circ}C$, and the values of CIE-L*a*b* parameters were L* = 44.62, a* = 3.10, and b* = 17.25. In the case of the pigment synthesized at $1500^{\circ}C$, the brown color was obtained at 0.01 mole and 0.02 mole $Cr_2O_3$, and the CIE-L*a*b* values were 55.34, 1.73, 28.64, and 49.39, 0.51, 21.33, respectively. At $1500^{\circ}C$, the maximum limit of solid solution was 0.03 mole $Cr_2O_3$. The glazed sample showed green color, and the values of the CIEL* a*b* parameters were L* = 45.69, a* = -0.98, and b* = 20.38.

CaO MgO.$2SiO_2-Al_2O_3$ 계의 고용체 생성에 관한 연구 (A Study on the Forming of Solid Solution in CaO.MgO.$2SiO_2-Al_2O_3$ System)

  • 안영필;김복희
    • 한국세라믹학회지
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    • 제20권1호
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    • pp.25-30
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    • 1983
  • This experiment was studied in the system of (1-x) CaO MgO $2SiO-Al_2O_3$ to investigate forming of solid solution. The technique empolyed was the well known water-quenching method. Differential thermal analysis of the each glass water quenched indicated that under 30 mole% $Al_2O_3$ was lowered with increasing of the amount of $Al_2O_3$ It was supposed by X-ray diffraction patterns of each specimen sintered at various temperature that only solid solution was formed under the 30mole % $Al_2O_3$ compositions solid solution and anorthite were formed at the 20mole% $Al_2O_3$ composition anorthite solid solution and spinel$(MgAl_2O_4)$ were formed over the 40mole% $Al_2O_3$ compositions. The maximum density and thermal expanison coefficient was 2.89g/cm 7.74x106./C$^{\circ}$ respectively in the composi-tion of 10 mole% $Al_2O_3$ . All the specimens showed linear thermal expansion behavior. Microhardness was as high as 850kg/nm2 in the composition of 5, 10, 20 mole % $Al_2O_3$ and dielectric constant was 7.3-6.9.

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ZrO2/Al2O3 박막의 고온산화 (High-temperature Oxidation of ZrO2/Al2O3 Thin Films)

  • Park, Soon Young;Yadav, Poonam;Abro, Muhammad Ali;Lee, Dong Bok
    • 한국표면공학회:학술대회논문집
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    • 한국표면공학회 2014년도 추계학술대회 논문집
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    • pp.117-117
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    • 2014
  • Thin $ZrO_2/Al_2O_3$ films were deposited on a tool steel substrate using Zr and Al cathodes in a cathodic arc plasma deposition system (CAPD), and then oxidized at $600-900^{\circ}C$ in air for up to 50 h. They effectively suppressed the oxidation of the substrate up to $800^{\circ}C$ by acting as a barrier layer against the outward diffusion of the substrate elements and inward diffusion of oxygen. However, rapid oxidation occurred at $900^{\circ}C$ due mainly to the increased diffusion and subsequent oxidation of steel as well as the crystallization of amorphous $Al_2O__3$.

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플라즈마/촉매 공정을 이용한 n-헵테인과 일산화탄소 동시제거 (Combined Removal of n-heptane and CO using Plasma-catalytic Process)

  • 이상백;조진오;목영선
    • 한국가스학회지
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    • 제20권2호
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    • pp.1-9
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    • 2016
  • 본 연구는 플라즈마/촉매 공정을 이용하여 n-헵테인과 일산화탄소의 동시제거에 대해 조사하였다. n-헵테인과 일산화탄소의 분해특성을 파악하기 위해 플라즈마/촉매 공정과 촉매공정의 분해효율을 비교하였고, 촉매의 종류, 온도, 전력 등을 변화시켜 실험을 진행하였다. n-헵테인의 분해효율은 반응기 내부의 온도보다는 에너지밀도에 더 영향을 많이 받는 것으로 확인되었으며, 일산화탄소는 에너지밀도와 반응기 내부 온도 모두의 영향을 받는 것으로 나타났다. 촉매의 종류를 달리하며 n-헵테인의 분해효율을 조사한 결과 $Pd/{\gamma}-Al_2O_3$ > $Ru/{\gamma}-Al_2O_3{\approx}Ag/{\gamma}-Al_2O_3$순으로 나타났다. 특히, $Pd/{\gamma}-Al_2O_3$를 사용한 경우 n-헵테인 분해 과정에서 일산화탄소가 거의 발생하지 않았으며, $CO_2$ 선택도가 100%에 가까웠다. 일산화탄소 분해효율은 $Pd/{\gamma}-Al_2O_3$ > $Ru/{\gamma}-Al_2O_3$ > $Ag/{\gamma}-Al_2O_3$ 순으로 나타났으며, $180^{\circ}C$이하의 온도에서는 플라즈마/촉매 공정의 효율이 높고, $180^{\circ}C$이상에서는 촉매 공정의 분해효율이 높았다.

저품위 Bauxite로부터 고순도 Al2O3의 합성(II) (Synthesis of High Purity Al2O3 from Low Grade Bauxite Ore(II))

  • 권긍택;송연호;이철태
    • 공업화학
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    • 제5권4호
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    • pp.597-608
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    • 1994
  • $(NH_4)_2SO_4$와 저품위 bauxite의 황산화 반응에 따라 얻어진 ammonium aluminium sulfate로부터 수열균일침전을 통해 무정형 alumina gel수화물 및 결정형 boehmite를 합성하고 이로 부터 고순도 $Al_2O_3$를 제조하는 새로운 공정 개발을 시도하였다. 이 공정은 ammonium aluminium sulfate용액 중의 Fe 성분을 제거하기 위한 용매추출공정과 정제된 ammonium aluminium sulfate용액으로부터 균일침전에 의한 Al 함유 침전물의 생성에 관한 것으로 이루어져 있다. 추출제 Alamine 336에 의한 적절한 용매추출조건은 shaking time 4분, 수상에 대한 유기상의 비 0.25였다. Urea를 이용한 수열균일 침전반응은 Al 함유용액 중의 Al에 대한 urea의 당량비 6.0의 조건에서 반응온도 $100^{\circ}C$ 이하에서는 무정형 alumina gel 수화물, $120^{\circ}C$ 이상 $150^{\circ}C$ 이하에서는 pseudo boehmite 그리고 $150^{\circ}C$ 이상에서는 결정형 boehmite가 합성되었다. 이 합성된 무정형 alumina gel 수화물은 소성시간 2시간, 소성온도 $1000^{\circ}C$ 이상에서 그리고 결정형 boehnite는 소성시간 2시간, 소성온도 $1250^{\circ}C$ 이상에서 ${\alpha}-Al_2O_3$로 전이되며 얻어진 ${\alpha}-Al_2O_3$의 순도는 99.97%의 고순도였다.

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열분석에 의한 $CaO.Al_2O_3.2SiO_2$ 유리의 결정화 고찰 (Crystallization Behavior of $CaO.Al_2O_3.2SiO_2$ Glass with Kinetic Parameters)

  • 이승한;류봉기;박희찬
    • 한국세라믹학회지
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    • 제31권12호
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    • pp.1545-1551
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    • 1994
  • Various kinetic parameters of the nucleation and crystallization in anorthite glass (CaO.Al2O3.2SiO2) were calculated by nonisothermal differential thermal analysis. Base glass and glass with TiO2 were prepared by melting. In base glass, the temperature where nucleation can occur ranges from 85$0^{\circ}C$ to 9$25^{\circ}C$ and the temperature for maximum nucleation was 900$\pm$5$^{\circ}C$. In glass with TiO2, the nucleation temperature range was 800~875$^{\circ}C$ and the maximum nucleation temperature was 850$\pm$5$^{\circ}C$. Kissinger equation, Bansal equation, and modified Ozawa equation were used for calculating activation energy for crystallization, Ec. The results showed the same activation energies for both glasses with and without TiO2 in the different equations. The shape of maximum exotherm peak and Ozawa equation were used for Avrami exponent, n. The n value for each glass was 2, indicating that each glass crystallized primarily by bulk crystallization.

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HAp와 알루미나 결합에 있어서의 중간 유리상 연구 (THE INTERMEDIATE GLASS STUDY IN HYDROXYAPATITE AND ALUMINA BONDING)

  • 김택남;김종옥;조성준
    • 자연과학논문집
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    • 제8권1호
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    • pp.47-51
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    • 1995
  • 알루미나와 Hydroxyapatite(HAp)의 결합을 연구하기 위하여 9 가지의 중간 유리상을 연구하였다. 그 중간상의 화학 조성은 $CaO-Al_2O_3$에서 정하였으며 CaO/$Al_2O_3$의 몰 비율은 0.5에서 3 까지 변화 시켰다. 가장 낮은 용융은 CaO/$Al_2O_3$의 몰 비율이 2이고 $1355^{\circ}C$때 나타났다. $Al_2O_3$의 양을 증가시킴에 따라 용융점은 점점 높아 졌고 많은 기공들이 발견 되었다. 단면 조직 조사에 따르면 높은 CaO양 시편에서 양호한 흡수접착을 발견할 수 있었고, 이것은 CaO/$Al_2O_3$ 비가 2보다 큰것에서 더좋은 흡수접착을 얻을 수 있음을 의미한다. 열처리후 상변태는 발견되었으나, HAp의 중요한 피크는 그대로 남아 있음을 알 수 있다.

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