• Title/Summary/Keyword: Al-3

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Solvothermal Synthesis of α-Al2O3 from Boehmite with Seeding Technique

  • Jo, Hye Youn;Park, Min-Gyeong;Lee, Seung-Ho;Kim, Dae Sung;Lee, Young Kwan;Lim, Hyung Mi
    • 한국세라믹학회지
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    • 제52권4호
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    • pp.273-278
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    • 2015
  • ${\alpha}-Al_2O_3$ was synthesized by solvothermal synthesis using ${\alpha}-Al_2O_3$ seed, precursor of fine boehmite (Al(OOH)) or gibbsite ($Al(OH)_3$), and 1, 4-butanediol solvent. The seed content and precursor type were selected as variables in order to synthesize ${\alpha}-Al_2O_3$. The formation time of ${\alpha}-Al_2O_3$ was reduced and the size of the particles was decreased with addition of the seed. When the seed content was increased, the size of the synthesized ${\alpha}-Al_2O_3$ was reduced. Morphologies of the as-synthesized ${\alpha}-Al_2O_3$ with ${\alpha}-Al_2O_3$ seed were polyhedron-shaped, while the shape was plate-like or polyhedral without the seed, depending on the additives or the average particle size of the boehmite precursor. The aggregation of as-synthesized ${\alpha}-Al_2O_3$ from boehmite was smaller than that from gibbsite. As-synthesized ${\alpha}-Al_2O_3$, with 140 nm size, was obtained by using the seed and boehmite precursor.

기계적 합금화 방법에 의해 제조된 $Ll_2$$Al_3$Ti금속간 화합물의 열적 안정성에 미치는 Mn의 첨가 영향에 관한 연구 (A Study on the Thermal Stability of $Ll_2$$Al_3$Ti Intermetallic Compounds Fabricated by Mechanical Alloying with Mn additions)

  • 최재웅;박종범;강성군
    • 한국재료학회지
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    • 제11권5호
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    • pp.393-397
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    • 2001
  • 고온구조용 재료로의 사용이 기대되는 $Al_3$Ti금속간 화합물의 연성 향상을 위한 목적으로 기계적 합금화를 통한 cubic Ll$_2$구조의 생성거동과 Mn의 첨가 영향을 조사하였다. Al-8Mn-25Ti조성에서 20시간의 기계적 합금화를 통해 약 1.0nm 사이즈의 grain을 갖는 nanocrystalline cubic Ll$_2$Al$_3$Ti 금속간 화합물이 제조되었다. Mn이 첨가된 3원계 cubic Ll$_2$Al$_3$Ti 금속간 화합물은 2원계 cubic Ll$_2$Al$_3$Ti 금속간 화합물에서 보이는 Ll$_2$구조에서 D0$_{23}$구조나 D0$_{22}$구조로의 상변태가 발생하지 않았으며 Mn의 첨가로 인해 Ll$_2$구조는 120$0^{\circ}C$가지 안정함을 보였다.

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SHS법을 이용한 복합분말(Al2O3-SiC) 제조시 TiO2첨가의 영향 (The effect of the addition of TiO2 in the preparation of (Al2O3-SiC)- SiC composite powder by SHS Process)

  • 윤기석;양범석;이종현;원창환
    • 한국재료학회지
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    • 제12권1호
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    • pp.48-53
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    • 2002
  • $Al_2O_3-SiC$ and $Al_2O_3-SiC$-TiC composite powders were prepared by SHS process using $SiO_2,\;TiO_2$, Al and C as raw materials. Aluminum powder was used as reducing agent of $SiO_2,\;TiO_2$ and activated charcoal was used as carbon source. In the preparations of $Al_2O_3-SiC$, the effect of the molar ratio in raw materials, compaction pressure, preheating temperature and atmosphere were investigated. The most important variable affecting the synthesis of $Al_2O_3-SiC$ was the molar ratio of carbon. Unreactants remained in the product among all conditions without compaction. The optimum condition in this reaction was $SiO_2$: Al: C=3: 5: 5.5, 80MPa compaction pressure under Preheating of $400^{\circ}C$ with Ar atmosphere. However there remains cabon in the optimum condition. The effect of $TiO_2$ as additive was investigated in the preparations of $Al_2O_3-SiC$. As a result of $TiO_2$ addition, $Al_2O_3-SiC$-TiC composite powder was prepared. The $Al_2O_3$ powder showed an angular type with 8 to $15{\mu}m$, and the particle size of SiC powder were 5~$10{\mu}m$ and TiC powder were 2 to $5{\mu}m$.

Hydroxyapatite와 Al2O3 혼합분말의 상압소결에 의한 TCP/Al2O3 및 Fluorapatite/Al2O3 복합재료의 In-Situ 제조 (In-Situ Fabrication of TCP/Al2O3 and Fluorapatite/Al2O3 Composites by Normal Sintering of Hydroxyapatite and Al2O3 Powder Mixtures)

  • 하정수;한유정
    • 한국재료학회지
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    • 제29권2호
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    • pp.129-135
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    • 2019
  • A powder mixture of 70 wt% $Al_2O_3$ and 30 wt% hydroxyapatite (HA) is sintered at $1300^{\circ}C$ or $1350^{\circ}C$ for 2 h at normal pressure. An $MgF_2$-added composition to make HA into fluorapatite (FA) is also prepared for comparison. The samples without $MgF_2$ show ${\alpha}$ & ${\beta}$-tricalcium phosphates (TCPs) and $Al_2O_3$ phases with no HA at either of the sintering temperatures. In the case of $1,350^{\circ}C$, a $CaAl_4O_7$ phase is also found. Densification values are 69 and 78 %, and strengths are 156 and 104 MPa for 1,300 and $1,350^{\circ}C$, respectively. Because the decomposition of HA produces a $H_2O$ vapor, fewer large pores of $5-6{\mu}m$ form at $1,300^{\circ}C$. The $MgF_2$-added samples show FA and $Al_2O_3$ phases with no TCP. Densification values are 79 and 87 %, and strengths are 104 and 143 MPa for 1,300 and $1,350^{\circ}C$, respectively. No large pores are observed, and the grain size of FA ($1-2{\mu}m$) is bigger than that of TCP ($0.7{\mu}m{\geq}$) in the samples without $MgF_2$. The resulting $TCP/Al_2O_3$ and $FA/Al_2O_3$ composites fabricated in situ exhibit strengths 6-10 times higher than monolithic TCP and HA.

ALD법으로 제조된 Al2O3 박막의 물리적 특성 (Physical Properties of the Al2O3 Thin Films Deposited by Atomic Layer Deposition)

  • 김재범;권덕렬;오기영;이종무
    • 한국재료학회지
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    • 제12권6호
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    • pp.493-498
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    • 2002
  • $Al_2O_3$ is a promising gate dielectric because of its high dielectric constant, high resistivity and low leakage current. Since $OH^-$ radical in $Al_2O_3$ films deposited by ALD using TMA and $H_2O$ degrades the good properties of $Al_2O_3$, TMA and $O_3$ were used to deposite $Al_2O_3$ films and the effects of $O_3$ on the properties of the $Al_2O_3$ films were investigated. The growth rate of the $Al_2O_3$ film under the optimum condition was 0.85 $\AA$/cycle. According to the XPS analysis results the $OH^-$ concentration in the $Al_2O_3$ film deposited using $O_3$ is lower than that using $H_2O$. RBS analysis results indicate the chemical formula of the film is $Al_{2.2}O_{2.8}$. The carbon concentration in the film detected by AES is under 1 at%. SEM observation confirms that the step coverage of the $Al_2O_3$ film deposited by ALD using $O_3$ is nearly 100%.

비정질 $SiO_2$${alpha}-Al_2O_3$부터 Mullite를 합성하기 위한 고체상태 반응속도 (Solid-state reaction kinetics for the formation of mullite($3Al_2O_3{\cdot}2SiO_2$) from amorphous $SiO_2$ and ${alpha}-Al_2O_3$)

  • 김익진;곽효섭;고영신
    • 한국결정성장학회지
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    • 제8권2호
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    • pp.332-341
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    • 1998
  • ${\alpha}-Al_2O_3$와 비정질 SiO2부터 Mullite를 합성하기 위한 고체상태반응의 반응속도를 1450~$1480^{\circ}C$ 온도 범위에서 연구하였다. 반응속도는 $Al_2O_3$분말을 코팅한 28.16wt%의 $SiO_2$와 일정한 온도에서 여러 시간동안 가열하여 생성된 혼합물에 의하여 결정되었다. MgO안의 반응물과 미반응물의 양은 X-선 회절분석에 의하여 결정되었다. Mullite의 부피율과 peak intensity 비의 자료로부터 $Al_2O_3$$SiO_2$$3Al_2O_3\;{\cdot}\;2SiO_2$형태로의 반응은 $1450^{\circ}C$$1480^{\circ}C$ 사이에서 시작되었다. 고체상태반응 활성화 에너지는 Arrhenius 식에 의하여 결정되었다. 활성화 에너지는 31.9KJ/mol이다.

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Ti(Al,O)/$Al_2O_3$ 플라즈마 코팅한 SS41의 고온산화 거동 (High Temperature Oxidation Behavior of Plasma-sprayed Ti(Al,O)/$Al_2O_3$ Coatings on SS41 Steel)

  • 최갑송;우기도;이현범;전재열
    • 열처리공학회지
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    • 제20권5호
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    • pp.231-236
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    • 2007
  • High velocity oxy-fuel (HVOF) spraying was used to coat Ti(Al,O)/$Al_2O_3$ powder onto the SS41 steel plate. Macrostructure of the coated specimen has been investigated by scanning electron micrograph (SEM). High temperature oxidation behavior of the coated specimen and SS41 steel have been studied. From the results of SEM observation, Ti(Al,O)/$Al_2O_3$ powder was coated well onto the substrate SS41 steel. Porosity onto the coated layer was only 0.38%. The oxidation results showed that Ti(Al,O)/$Al_2O_3$ powder coated SS41 steel have improved little oxidation resistance at $900^{\circ}C$ in air, but improved remarkably oxidation resistance at $800^{\circ}C $ in air compare to the substrate SS41 steel.

Si-Al-SiO2-NH4F(β-Si3N4)계에서 연소반응에 의한 β-SiAlON분말의 제조 (Preparation of β-SiAlON Powder by Combustion Reaction in the System of Si-Al-SiO2-NH4F(β-Si3N4))

  • 민현홍;신창윤;원창환
    • 한국세라믹학회지
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    • 제43권10호
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    • pp.595-600
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    • 2006
  • The preparation of $\beta$-SiAlON powder by SHS in the system of $Si-Al-SiO_2-NH_4F(\beta-Si_3N_4)$ was investigated in this study. In the preparation of SiAlON powder, the effect of gas pressure, compositions such as Si, $NH_4F$, \beta-Si_3N_4$ and additive in mixture on the reactivity were investigated. At 50 atm of the initial inert gas pressure in reactor, the optimum composition for the preparation of pure $\beta$-SiAlON was $3Si+Al+2SiO_2+NH_4F$. The $\beta$-SiAlON powder synthesized in this condition was a single phase $\beta$-SiAlON with a rod like morphology.

Al2(SO4)3.18H2O로부터 AlN 분말의 합성: I. 침전법 (Synthesis of AlN Powder from Al2(SO4)3.18H2O: I. Precipitation Method)

  • 이홍림;송태호
    • 한국세라믹학회지
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    • 제28권6호
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    • pp.465-470
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    • 1991
  • AlN powder was synthesized by carbothermal reduction and nitridation of aluminum hydroxides precipitated in 5∼11 pH range from Al2(SO4)3$.$18H2O aqueous solution. Nitridation reactivity of hydroxide, which depends on precipitation pH, reaction temperature and time, was examined by XRD analysis at 1200∼1350$^{\circ}C$ and compared with that of commercial ${\alpha}$-Al2O3. Hydroxides obtained at higher pH could be more easily nitridated and, considering DTA/TG and BET results, the reason seems to be specific surface area difference of reactants depending on the content of decomposed structural water and the transition rate from transition-Al2O3 to ${\alpha}$-Al2O3.

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