• 제목/요약/키워드: c-$Al_2O_3$

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$Al_{2}O_{3}+Y_{2}O_{3}$를 첨가한 $\beta$-SiC-$ZrB_2$ 복합체의 특성 (Properties of the $\beta$-SiC-$ZrB_2$ Composites with $Al_{2}O_{3}+Y_{2}O_{3}$ additives)

  • 신용덕;주진영
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 1998년도 추계학술대회 논문집 학회본부 C
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    • pp.853-855
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    • 1998
  • The electrical resistivity and mechanical properties of the hot-pressed and annealed ${\beta}$-SiC+39vol.%$ZrB_2$ electroconductive ceramic composites were investigated as a function of the liquid forming additives of $Al_{2}O_{3}+Y_{2}O_{3}$(6:4wt%). In this microstructures. no reactions were observed between $\beta$-SiC and $ZrB_2$, and the relative density is over 97.6% of the theoretical density. Phase analysis of composites by XRD revealed mostly of a $\alpha$-SiC(6H, 4H), $ZrB_2$ and weakly $\beta$-SiC(15R) phase. The fracture toughness decreased with increased $Al_{2}O_{3}+Y_{2}O_{3}$ contents and showed the highest for composite added with 4wt% $Al_{2}O_{3}+Y_{2}O_{3}$ additives. The electrical resistivity increased with increased $Al_{2}O_{3}+Y_{2}O_{3}$ contents because of the increasing tendency of pore formation according to amount of liquid forming additives $Al_{2}O_{3}+Y_{2}O_{3}$. The electrical resistivity of composites is all positive temperature coefficient resistance(PTCR) against temperature up to $700^{\circ}C$.

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SiC 휘스커 강화 Al2O3 복합재료의 고인화 (Toughening of SiC Whisker Reinforced Al2O3 Composite)

  • 김연직;송준희
    • 한국재료학회지
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    • 제14권9호
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    • pp.649-654
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    • 2004
  • In this paper, the fracture toughness and mechanisms of failure in a random SiC-whisker/$Al_{2}O_3$ ceramic composite were investigated using in situ observations during mode I(opening) loading. $SiC_{w}/Al_{2}O_3$ composite was obtained by hot press sintering of $Al_{2}O_3$ powder and SiC whisker as the matrix and reinforcement, respectively. The whisker and powder were mixed using a turbo mill. The composite was produced at SiC whisker volume fraction of $0.3\%$. Compared with monolithic $Al_{2}O_3$, fracture toughness enhancement was observed in $SiC_{w}/Al_{2}O_3$ composite. This improved fracture toughness was attributed to SiC whisker bridging and crack deflection. $SiC_{w}/Al_{2}O_3$ composite exhibited typically brittle fracture behavior, but a fracture process zone was observed in this composite. This means that the load versus load-line displacement curve of $SiC_{w}/Al_{2}O_3$ composite from a fracture test may involve a small non-linear region near the peak load.

불소성 $Al_2O_3-C$질 내화벽돌의 특성에 미치는 첨가물의 영향 (Effects of Additives on Properties of Unfired $Al_2O_3-C$ Bricks)

  • 홍기곤;채상택
    • 한국세라믹학회지
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    • 제31권7호
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    • pp.759-766
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    • 1994
  • The effect of additives on properties of unfired Al2O3-C bricks were investigated. The increase of carbon content and the addition of MgO or spinel improved the resistances against spalling and corrosion of unfired Al2O3-C bricks. Also, the oxidation resistance of unfired Al2O3-C brick was increased by adopting complex metals of Al and Si in spite of the increase of carbon content.

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AlN-SiO2-Al2O3계로부터 AlN-Polytypes의 제조 (Synthesis of AlN-SiO2-Al2O3 System)

  • 박용갑;장병국
    • 한국세라믹학회지
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    • 제26권1호
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    • pp.31-36
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    • 1989
  • In order to synthesize AlN-polytypes from AlN-SiO2-Al2O3 system, composition A (AlN/SiO2/Al2O3=1/0.3/0.05, mole ratio) and composition B(AlN-SiO2-Al2O3=1/0.2/0.05, mole ratio) were used. AlN-polytypes were produced by nitriding the mixture at 175$0^{\circ}C$~190$0^{\circ}C$ under N2 atmosphere. For lower reaction temperature, 15R phase was produced and in the case of higher reaction temperature, AlN phase was only produced. As each composition was heated at 185$0^{\circ}C$ in N2 atmosphere, produced main phases were 15R phase for composition A and 21R phase for composition B respectively. The fracture surfaces of produced reactants showed porous skeleton structure.

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반응소결법에 의한 $Al_2O_3/Fe$ 복합재료 제조 (Fabrication of$Al_2O_3/Fe$ composite by reaction sintering)

  • 김송희;윤여범
    • 한국결정성장학회지
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    • 제9권2호
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    • pp.185-190
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    • 1999
  • $Al_2O_3/Fe$ 복합재료 제조는 반응소결법에 의한 2단계 공정을 통해서 제조되었으며 이 공정은 장비가 간단하고 near-net-shape이 가능한 장점이 있다.$Al_2O_3/Fe$ 복합재료를 제조하기 위해서 1차로 $650^{\circ}C$에서 5시간동안 산화/환원 처리를 행하고 $1200^{\circ}C$에서 2차로 소결처리를 행하였다. 제조된 복합재료의 상분석결과 $\alpha$-Fe 와 $\alpha$-$Al_2O_3/Fe$가 주된 상이었고 소량의 $FeAl_2O_4$가 검출되었다. 이 소량의 $FeAl_2O_4$상은 Fe가 $Al_2O_4$기공을 채우는 것을 방해함으로써 소결동안 미세구조 내에 약간의 기공을 발생시킨다.

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SiC-Al2O3 촉매를 이용한 CF4의 마이크로파 열분해 (Microwave Thermal Decomposition of CF4 using SiC-Al2O3)

  • 최성우
    • 한국환경과학회지
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    • 제22권9호
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    • pp.1097-1103
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    • 2013
  • Tetrafluoromethane($CF_4$) have been widely used as etching and chemical vapor deposition gases for semiconductor manufacturing processes. $CF_4$ decomposition efficiency using microwave system was carried out as a function of the microwave power, the reaction temperature, and the quantity of $Al_2O_3$ addition. High reaction temperature and addition of $Al_2O_3$ increased the $CF_4$ removal efficiencies and the $CO_2/CF_4$ ratio. When the SA30 (SiC+30wt%$Al_2O_3$) and SA50 (SiC+50wt%$Al_2O_3$) were used, complete $CF_4$ removal was achieved at $1000^{\circ}C$. The $CF_4$ was reacted with $Al_2O_3$ and by-products such as $CO_2/CF_4$ and $AlF_3$ were produced. Significant amount of by-product such as $AlF_3$ was identified by X-ray powder diffraction analysis. It also showed that the ${\gamma}-Al_2O_3$ was transformed to ${\alpha}-Al_2O_3$ after microwave thermal reaction.

$Al_2O_3/SiC$ 나노복합체의 상압소결 및 역학적 특성에 미치는 볼밀분쇄와 소결온도의 영향 (The Effect of Ball Milling and Sintering Temperatures on the Sintering Behaviors and Mechanical Properties of $Al_2O_3/SiC$ Nanocomposites)

  • 류정호;나석호;이재형;조성재
    • 한국세라믹학회지
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    • 제34권6호
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    • pp.668-676
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    • 1997
  • Al2O3/SiC nanocomposites are fabricated through intensive ball milling to mix fine SiC particles uniformly with the Al2O3 powder. Another role of milling is to reduce particle sizes by crushing particles as well as agglomerates. However, balls are worn during ball milling and the sample powder mixtures pick up to weight loss of the balls. In this study, pressureless sintering was performed to obtain Al2O3/SiC nanocomposites. It was found that the wear rate of zirconia balls during milling was considerable, and the zirconia addition after even a few hours of ball milling could increase the sintering rates of the nanocomposites significantly. Thus, addition of ZrO2 changed the sintering behaviors as well as mechanical properties of Al2O3/SiC nanocomposites.

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$Al_2O_3-SiC$ 나노복합체의 방전 플라즈마 소결 특성 및 기계적 물성 (Sintering behavior and mechanical properties of the $Al_2O_3-SiC$ nano-com-posite using a spark plasma sintering technique)

  • 채재홍;김경훈;심광보
    • 한국결정성장학회지
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    • 제13권6호
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    • pp.309-314
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    • 2003
  • 방전 플라즈마 소결법을 적용하여 $Al_2O_3$-SiC 나노 복합체를 150$0^{\circ}C$ 이하의 온도에서 완전치밀화를 이루었다. 제조된 $Al_2O_3$-SiC 복합체는 이상 결정립 성장 없이 매우 균질한 미세구조를 형성하고 있는데, 첨가된 SiC 입자는 주로 결정립 내 및 결정립계에 존재하면서 $Al_2O_3$기지상에서 결정립 성장을 억제하는데 매우 유호하였음을 확인 할 수 있다. 한편, SiC 입자의 첨가는 크랙 회절 및 브릿징 등에 의해서 유도된 재료 강도 및 인성 강화 기구에 의해서 $Al_2O_3$-SiC 복합체의 기계적 물성을 크게 향상시켰다.

반응 금속 침투법에 의한 $Al/Al_2O_3$복합체의 제조 및 기계적 특성 (Fabrication and mechanical properties of $Al/Al_2O_3$ composites by reactive metal penetration method)

  • 윤영훈;홍상우;최성철
    • 한국결정성장학회지
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    • 제11권6호
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    • pp.239-245
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    • 2001
  • 뮬라이트 preform과 비정질 실리카를 알루미늄 용융체에서 $1100^{\circ}C$, 5시간 동안 반응시켜 $Al/Al_2O_3$복합체가 제조되었다. 뮬라이트 preform과 알루미늄 용융체 간의 화학적 반응은 상호 연결된 미세구조를 형성하였다. $Al/Al_2O_3$복합체의 금속의 양은 뮬라이트 preform의 소결 온도($1600^{\circ}C$, $1625^{\circ}C$, $1650^{\circ}C$, $1700^{\circ}C$)에 따른 겉보기 기공율의 변수로서 조절되었으며, 복합체의 기계적 특성들은 알루미늄 양에 따라 조사되었다. $1600^{\circ}C$ 이상의 온도에서 소결된 뮬라이트 preform은 침투된 알루미늄 용융체와 화학반응을 이루었으나, $1600^{\circ}C$에서 소결된 뮬라이트 소결체는 알루미늄 용융체에 대해 젖음이 이루어지지 않아 화학반응이 진행되지 않았다. 알루미늄 용융체의 침투 방향에 따른 복합체의 기계적 특성에 대한 영향은 알루미늄 용융체의 수직, 평행한 침투 방향 패턴의 두 가지 다른 모델들에 의해 고려되었다. $Al/Al_2O_3$복합체에서 알루미늄의 양의 증가에 따라 파괴강도는 감소하였으며, 파괴인성은 증가하는 경향을 나타냈다.$ Al/Al_2O_3$복합체의 미세구조는 금속의 침투 방향에 의해 결정되었지만, 복합체의 파괴강도와 파괴인성은 금속 침투 방향에 대한 의존성은 나타내지 않았다.

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CH4 Dry Reforming on Alumina-Supported Nickel Catalyst

  • Joo, Oh-Shim;Jung, Kwang-Deog
    • Bulletin of the Korean Chemical Society
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    • 제23권8호
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    • pp.1149-1153
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    • 2002
  • CH4/CO2 dry reforming was carried out to make syn gas on the Ni/Al2O3 catalysts calcined at different temperatures. The Ni/Al2O3 (850 $^{\circ}C)$ catalyst gave good activity and stability w hereas the Ni/Al2O3 $(450^{\circ}C)$ catalyst showed lower activity and stability. The NiO/Al2O3 catalyst calcined at $850^{\circ}C$ for 16 h (Ni/Al2O3 $(850^{\circ}C))$ formed the spinel structure of nickel aluminate, which was confirmed by TPR. The carbon formation rate on the Ni/Al2O3 $(850^{\circ}C)$ catalyst was very low till 20 h, and then steeply increased with reaction time without decreasing the activity for CH4 reforming. The Ni/Al2O3 $(450^{\circ}C)$ catalyst showed high carbon formation rate at the initial reaction time and then, the rate nearly stopped with continuous decreasing the activity for CH4 reforming. Even though the amount of carbon deposition on the Ni/Al2O3 $(850^{\circ}C)$ catalyst was higher than that on the Ni/Al2O3 $(450^{\circ}C)$ catalyst, the activity for CH4ing was also high, which could be attributed to the different type of the carbon formed on the catalyst surface.