• 제목/요약/키워드: ${\beta}-SiC$ 분말

검색결과 64건 처리시간 0.032초

β-SiC 분말 Seeds가 Sol-gel 공정으로 합성된 고순도 β-SiC 분말 형상 및 크기에 미치는 영향 (Effects of β-SiC Particle Seeds on Morphology and Size of High Purity β-SiC Powder Synthesized using Sol-Gel Process)

  • 김규미;조경선;박상환
    • 한국세라믹학회지
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    • 제46권5호
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    • pp.528-533
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    • 2009
  • High purity $\beta$-SiC powders were synthesized using sol-gel processing. TEOS and phenol resin were used as the starting material for the silicon source and carbon source, respectively. The process turned out to be capable of producing high purity SiC powder purity degree with 99.98 %. However, it was difficult to control the shape and size of $\beta$-SiC powders synthesized by sol-gel process. In this study, $\beta$-SiC powder with size of $1{\sim}5$ um an 30 nm were used as the seeds for $\beta$-SiC to control the $\beta$-SiC powder morphology. It was found that $\beta$-SiC powder seeds was effective to increase the powder average size of synthesized $\beta$-SiC using sol-gel process by acting as the preferred growing sites for $\beta$-SiC.

그라파이트 블록을 원료로써 재활용한 β-SiC 분말 합성 (Synthesis of β-SiC Powder using a Recycled Graphite Block as a Source)

  • 민닷 응우옌;방정원;김수룡;김영희;정은진;황규홍;권우택
    • 자원리싸이클링
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    • 제26권1호
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    • pp.16-21
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    • 2017
  • 본 연구는 SiC 결정 성장을 위한 원료 분말 합성법에 관한 것이다. ${\beta}-SiC$ 분말들은 높은 온도 조건(>$1400^{\circ}C$)에서 실리콘 분말과 탄소 분말의 반응에 의해서 합성 된다. 이 반응은 진공 상태(또는 Ar 가스 분위기)에서 실리콘+탄소 혼합물이 반응하고 다결정의 SiC 분말을 형성하기 충분한 횟수를 거쳐 그라파이트 도가니 안에서 진행된다. 최종 결과물의 특성들은 X-ray 회절, SEM/EDS, 입도 분석 및 ICP-OES을 통해 분석되었다. 또한, 최종 결과물의 순도는 the Korean Standard KS L 1612에 의거해서 분석했다.

기상반응에 의한 SiC-${Si_3}{N_4}$복합 분말의 제조 및 결정화 (Synthesis and Crystallization of Fine SiC-${Si_3}{N_4}$Composite Powders by the Vapor Phase Reaction)

  • 김형인;최재문;김석;소명기
    • 한국세라믹학회지
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    • 제37권11호
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    • pp.1091-1096
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    • 2000
  • 본 연구에서는 기상 반응법을 이용하여 TMS(Tetramethylsilane:Si($CH_3$)$_4$)와 NH$_3$그리고 H$_2$의 혼합기체로부터 반응 온도 1000~120$0^{\circ}C$ 및 입력비(NH$_3$/Si($CH_3$)$_4$) 1~3의 조건에서 초미분의 SiC-Si$_3$N$_4$복합 분말을 합성하였다. 합성되어진 복합 분말들의 결정상의 변화와 평균 입경을 알아보기 위해 XRD와 TEM 분석을 행한 결과, 구형의 비정질 분말이 형성되었으며, 입자의 크기는 약 70~130nm이었다. 입자의 크기는 입력비에 관계없이 거의 일정하였으나 반응 온도가 증가함에 따라서 감소하였다. FT-IR과 EA 분석 결과, 합성되어진 분말은 Si, N, C, 그리고 H로 이루어진 화합물임을 확인할 수 있었다. 또한 입력비가 다른 조건에서 합성되어진 분말을 $N_2$분위기 하에서 155$0^{\circ}C$로 2시간 열처리를 행한 결과, 낮은 입력비인 경우 $\beta$-SiC, $\alpha$-Si$_3$N$_4$$\beta$-Si$_3$N$_4$의 결정상들이 혼재하였으나, 높은 입력비인 경우는 결정화 후 $\alpha$-Si$_3$N$_4$상만이 존재하였다.

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$\alpha-SiC $seed의 첨가가 상압소결된 $\beta-SiC$의 미세구조와 파괴인성에 미치는 영향 (Effect of $\alpha-SiC $seed on microstructure and fracture toughness of pressureless-sintered $\beta-SiC$)

  • Young-Wook Kim;Won-Joong Kim;Kyeong-Sik Cho;Heon -Jin Choi
    • 한국결정성장학회지
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    • 제7권1호
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    • pp.18-26
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    • 1997
  • 소결조제로 Y 3Alo012를 첨가한 {3- SiC 분말에 seed로서 1 wt%의 a- SiC 분말을 첨 가한 시편과 첨가하지 않은 시편을 1950$^{\circ}$C, argon 분위기에서 0.5~4시간 동안 소결하였다. S Seed로써 1 wt% a-SiC 분말의 첨가는 소결 도중에 길게 자란 업자틀의 성장을 가속시켰고, a a- SiC seed를 첨가한 시편에서 더 조대한 미세구조가 얻어졌다 .. a-SiC seed를 첨가하여 4시간 동안 소결한 시편의 파괴인성은 7.5 MPa'ml/2이었고, seed를 첨가하지 않은 시편의 파괴인성은 6 6.1 MPa'm1/2이었다 .. Seed를 첨가한 시편의 높은 파괴인성은 조대한 미세구조에 포함된 길게 자란 입자들에 의한 균열가교 기구의 활발한 작용에 기인한다.

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제천규석으로부터 SiC 및 $SiC-Si_3N_4$계 분말 합성 (Syntheses of SiC and $SiC-Si_3N_4$ Powder from Jecheon Quartz)

  • 이홍림;배철훈;문준화
    • 한국세라믹학회지
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    • 제23권1호
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    • pp.67-73
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    • 1986
  • SiC and $SiC-Si_3N_4$ powder were synthesized via the carbiding and carbiding-nitriding reaction of Jecheon quartz respectively using graphite as a reducing agent. $\beta$-SiC+($\alpha$+$\beta$)-$Si_3N_4$ composite was obtained by the carbiding-nitriding reaction of Jecheon quartz-graphite mixture at 1, 35$0^{\circ}C$ in $H_2$ atmosphere. $\beta$-SiC+($\alpha$+$\beta$)-$Si_3N_4$ composite was obtained by the carbidint-nitriding reaction of Jecheon quartz-graphite mixture at 1, 35$0^{\circ}C$ in $N_2-H_2$ atmosphere. The ratio of $\beta$-SiC+($\alpha$+$\beta$)-$Si_3N_4$ content in a produced composite could be controlled by adjusting the reaction time and gaseous mixture.

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기계적 합금화법에 의한 ${\beta}-FeSi_2$ 분말 함성 (Synthesis of ${\beta}-FeSi_2$ Powder by Mechanical Alloying Process)

  • 이충효;조재문;김환태;권영순
    • 한국분말재료학회지
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    • 제8권2호
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    • pp.104-109
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    • 2001
  • The semiconducting ${\beta}-FeSi_2$ compound has been recognized as a thermoelectric material with excel-lent oxidation resistance and stable characteristics at elevated temperature. In the present work, we applied mechanical alloying(MA) technique to produce ${\beta}-FeSi_2$ compound using a mixture of elemental iron and silicon powders. The mechanical alloying was carried out using a Fritsch P-5 planetary mill under Ar gas atmosphere. The MA powders were characterized by the X-ray diffraction with Cu-K $\alpha$ radiation, thermal analysis and scanning electron microscopy. The single ${\beta}-FeSi_2$ phase has been obtained by mechanical alloying of $Fe_{33}Si_{67}$ mixture powders for 120 hrs or for 70 hrs coupled with the subsequent heat treatment up to $700^{\circ}C$. The grain size of ${\beta}-FeSi_2$ powders analyzed by Hall plot method was 44nm.

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Ethyl Silicate를 이용한 고순도 $\beta$-SiC미분말 합성에 관한 연구(II) (분말의 특성, 반응형식 및 활성화에너지) (A Studyon Synthesis of High Purity $\beta$-SiC Fine Particles from Ethyl Silicate(II) (Powder Properties, Reaction Type and Activation Energy))

  • 최용식;박금철
    • 한국세라믹학회지
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    • 제26권2호
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    • pp.195-200
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    • 1989
  • The Silica-Carbon mixture was made with addition of carbon black in the composition which monodispersed spherical fine silica was formed by the hydrolysis of ethylsilicate, mole ratio of Carbon/Alkoxide was 3.1 and $\beta$-SiC powder was synthesized by reacting this mixture at 1,350~1,50$0^{\circ}C$ in Ar atmosphere. The results of this study are as follow : (1) The purity of synthesized $\beta$-SiC powder was above 99.98% and it was in cubic modification with lattice constant of 4.3476$\AA$. (2) The rate-controlling steps varied with the reaction temperature for the syntehsis of $\beta$-SiC in this study ; nucleation and growth of $\beta$-SiC at 1,350~1,40$0^{\circ}C$, interfacial reaction at 1,45$0^{\circ}C$ and diffusion described by Jander Equation at 1,50$0^{\circ}C$. (3) When the rate-determining step was nucleation and growth, the activation energy was about 87.8kcal/mol.

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AlSiCa($Al_2O_3-SiC-C$)계 내화물 재료에 관한 연구: (I) 국산 chamotte로부터 원료분말합성 (On the Study Of AlSiCa($Al_2O_3-SiC-C$) refractories: (I) Synthesis of raw material using domestic chnmotte)

  • 심광보;주경;오근호
    • 한국결정성장학회지
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    • 제7권4호
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    • pp.626-631
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    • 1997
  • 하동고령토($Al_2O_3-SiC-C$)를 출발원료로하여 AlSiCa내화재 원료를 합성하였다. 하동고령토와 탄소분말을 혼합하여 수소분위기하에서 반응시킨결과, $1300^{\circ}C$에서$Al_2O_3-SiC-C$ 복합체가 힙성되기 시작하여$1400^{\circ}C$에서 완전 합성되었고, $SiO_2$에 대한 최적carbon량은 mole비로 1:4이었다. 합성시 알루미나 용기에 탄소분말을 충전시키지 않을 때는 미합성부분이 없이 밝은 녹색을 띈 $\beta$-SiC(cubic form) 를 형성함을 확인하였다.

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기상반응에 의한 $\beta$-SiC 초미분말 합성시 수소 가스유량과 TMS 농도의 영향 (The Effect of H2 Flow Rate and TMS Concentration on Synthesizing Ultrafine $\beta$-SiC Powder by Vapor Phase Reaction)

  • 유용호;어경훈;소명기
    • 한국세라믹학회지
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    • 제36권8호
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    • pp.853-858
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    • 1999
  • To investigate the effect of H2 flow rate and TMS[Si(CH3)4] concentration on synthesizing ultrafine ${\beta}$-SiC powder by vapor phase reaction the experiment was performed at 1100$^{\circ}C$ of the reaction temperature under the condition of 200-2000 cc/min of H2 gas flow rate and 1-10% of TMS concentration respectively. The shape of ${\beta}$-SiC particles synthesized was spherical and the size of particles decreased and the distribution of particles was more uniform with increasing H2 gas flow rate. In this case Si powders were coexisted with ${\beta}$-SiC Pure and ultrafine ${\beta}$-SiC powders without Si were obtained under the condition of above 2% of TMS concentration and below 1500 cc/min of H2 gas flow rate.

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알콕사이드로부터 Si-Al-O-N계 분말합성 I. 알콕사이드로부터 Si3N4와 $\beta$-Sialon 초미분말 합성 (Synthesis of Powder of the System Si-Al-O-N from Alkoxides I. Synthesis of Si3N4 and $\beta$-Sialon Ultrafine Powders from Alkoxides)

  • 이홍림;유영창
    • 한국세라믹학회지
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    • 제24권1호
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    • pp.23-32
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    • 1987
  • Synthesis of high purity ultrafine Si3N4 and ${\beta}$-Sialon powders was investigated via the simultaneous reduction and nitriding of amorphous SiO2, SiO2-Al2O3 system prepaerd by hydrolysis of alkoxides, using carbonablack as a reducing agent. In Si(OC2H5)4-C2H5 OH-H2 O-NH4OH system, hydrolysis rate increased with increasing reaction temperature and pH. Pure ${\alpha}$-Si3N4 was formed at 1350$^{\circ}C$ for 5 hrs in N2 atmosphere. In Si(OC2H5)4-Al(OC3H7)3-C6H6-H2 O-NH4OH system, weight loss increased as Si/Al ratio decreased. Single phase ${\beta}$-Sialon consisted of Si/Al=2 was formed at 1350$^{\circ}C$ in N2 and minor phases of ${\alpha}$-Si3N4, AIN, and X-phase were existed besides theSialon phase at other Si/Al ratios. The Si3N4 and Sialon powders synthesized from alkoxides consisted of uniform find particles of 0.05-0.2$\mu\textrm{m}$ in diameter, respectively.

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