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등온 저압화학기상침투법에 의한 탄소/탄소 복합재료의 치밀화에 대한 제조공정변수의 영향
박희동,안치원,조건,윤병일,김광수,Park, H.D.,Ahn, C.W.,Cho, K.,Yoon, B.Y.,Kim, K.S. 한국재료학회 1994 한국재료학회지 Vol.4 No.3
프로판($C_3H_8$)을 반응가스로 사용하여 등온 저압화학기상침투법(low-pressure chemical vapor infiltration)으로 탄소/탄소 복합재료를 치밀화 할 때 반응온도, 반응가스농도, 가스유량, 반응압력 등의 제조공정변수들이 치밀화에 미치는 영향을 알아보기 위하여 실험계획법(Rdbust design method)에 의한 실험을 행하였다. 1회의 등온 저압화학기상침투 실험으로 탄소/탄소 복합재료의 부피 밀도와 표면과 내부의 부피 밀도의 차이를 특성치(characteristic value)로 한 실험계획법의 분산분석(analysis of variance)에 의하면 반응온도, 반응가스농도, 가스유량 등의 제고공정변수가 치밀화에 기여도가 높으며, 반응압력의 기여도와 제조공정변수들의 교호작용(interaction)에 의한 기여도는 낮은 것으로 나타났다. 반응온도가 $1100^{\circ}C$, 반응가스농도가 100% $C_3H_8$, 가스유량이 100 SCCM, 반응압력이 5torr인 조건에서 탄소/탄소 복합재료는 가장 높은 부피 밀도값을 나타내었으나 시편의 표면과 내부의 부피 밀도 차이값은 컸다. The effect of processing parameters, temperature, gas concentration, gas flow rate and pressure, were studied on the densification of carbon/carbon composites using a Robust design method in isothermal low-pressure chemical vapor infiltration with a gas system of $C_3H_8-N_2$ After one time of isothermal low-pressure chemical vapor infiltrat.ion, the bulk density of carbon/carbon composites in creased up to 1-9% and apparent porosity of the composites decreased down to 20-50%. ANOVA analysis of the experiment.al data revealed that the important parameters of isothermal lowpressure chemical vapor infiltration were temperature, gas concentration and gas flnw rate. 'There was almost no ~ f f e c t on densification by pressure and interaction between each parameters. In t, he present experimental conditions, the highest bulk density was obtained at $1100^{\circ}C$ temperature, 100% $C_3H_8$, concentration, 100 SCCM flow rate and 5 torr pressure.
$TiB_2$ SHS 및 직접 접촉가열에 의한 동시 가압법 : 온도분포 모델링 및 공급에너지와 치밀화 관계
정진근,조건,이형복,Chung, G.K.,Cho, K.,Lee, H.B. 한국세라믹학회 1995 한국세라믹학회지 Vol.32 No.7
TiB2 was simultaneously synthesized and densified with concurrent self-propagating high-temperature synthesis and direct contact-heating by electrcial power input and pressure. Density of TiB2 synthesized by self-propagating high-temperature synthesis and consolidated simultaneously by direct contact-heating and pressure was maximum 80% of the theoretical density (4.52g/㎤). Temperature profile was analyzed by solving heat balance equation with numerical method (FTCS method). The temperature of the sample was sufficiently raised to that temperature sufficient to be densified. It was ascertained that the density of the SHS synthesized TiB2 is exponentially proportinal to the input thermal energy per mass.
저농도의 HPC 영역에서 에멀젼법에 의해 제조된 구형 알루미나 분말의 입자 크기 변화
안치원,박건식,유한수,조건,이영우,양명승,Ahn, C.W.,Park, K.S.,Yoo, H.S.,Cho, K.,Lee, Y.W.,Yang, M.S. 한국세라믹학회 1995 한국세라믹학회지 Vol.32 No.5
Spherical alumina gel powders were produced by hydrolysis of aluminum sec-butoxide (Al(sec-OC4H9)3) in a n-octanol/acetonitrile mixed solvent. The enlargement of particle size was induced by increasing HPC (hydroypropylcellulose) concentration (0.005, 0.1, and 0.05 g/ι) and emulsion-state aging time (10 min and 360 min). Mean particle sizes of dried alumina gel powders increased from 1.4 ${\mu}{\textrm}{m}$ to 3.5${\mu}{\textrm}{m}$ at 10-min emulsion-state aging time and from 1.9${\mu}{\textrm}{m}$ to 4.1${\mu}{\textrm}{m}$ at 360-min emulsion-state aging time as HPC concentration increased from 0.005 g/ι to 0.05 g/ι. At the same HPC concentration, particle size of dried alumina gel powder increased with increasing of emulsion-state aging time from 10 min to 360 min. The increase in the average particle size of dried alumina gel powder with increase in HPC concentration was interpreted as the enlargement of particles from alkoxide emulsions unprotected by HPC. The produced dried gel powder calcined at 115$0^{\circ}C$ for one hour transformed to $\alpha$-alumina.