• 한국결정성장학회지
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• 제8권2호
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• pp.324-331
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• 1998

2, 5, 10 mol% YAG(yttrium aluminum garnet) 분말을 액상 소결조제로 $\alpha$상 탄화규소 분말에 첨가한 후 $1850^{\circ}C$에서 소결시간을 달리하여 소결체를 제조한 다음, 소결시 일어나는 미세구조 변화를 첨가된 액상량과 소결시간의 변화에 대하여 고찰하였다. 각 조성중 2시간 소결한 시편에서 가장 높은 밀도를 나타냈으며, 소결시간이 길수록 액상의 기화로 인하여 중량감소량이 점차 증가하였다. 또한 첨가된 YAG 액상량이 증가할 수록 상대밀도(apparent density)와 중량감소량은 증가하였으나 입성장속도는 감소하였다. 액상량이 적은 시편에서는 소결시간이 길수록 일부 6H상의 탄화규소 입자가 4H상 탄화규소 입자로 상전이 되었으며, 이로 인하여 막대상 입자들이 일부 존재하였다.

• 한국세라믹학회지
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• 제41권9호
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• pp.715-721
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• 2004

합성 수산화아파타이트(HAp)와 바인더로서 젤라틴(GEL)을 사용하여 공침법으로 조성비가 서로 다른 HAp/GEL 균질복 합체 4종을 제조하였고, 이 균질복합체를 냉간정수압법으로 성형한 후 공기중에서 여러조건으로 소결하였다. HAp/GEL composite의 소결체는 XRD 및 FT-IR로 결정성 및 구조를 조사하였고, 또한 소결시편은 만능재료시험기(UTM)로 압축강도를 측정하였으며, 파단된 소결시편의 표면은 SEM으로 관찰하였다 HAp/GEL composite는 120$0^{\circ}C$에서 3시간 소결하였을 경우 부분적인 $\alpha$, $\beta$-tricalcium phosphate로 상전이가 일어났다. 소결체의 기공률은 1.2-30.2% 범위였고, 소결시편의 압축강도는 16.2-60.1㎫ 범위의 값을 나타냄으로써 기공율에 비해 높은 강도를 나타내었다.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2004년도 춘계학술강연 및 발표대회 강연 및 발표논문 초록집
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• pp.25-25
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• 2004

• 한국세라믹학회:학술대회논문집
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• 한국세라믹학회 2003년도 춘계총회 및 연구발표회 초록집
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• pp.61.2-61
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• 2003

• 한국세라믹학회:학술대회논문집
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• 한국세라믹학회 2003년도 추계총회 및 연구발표회 초록집
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• pp.67.2-67
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• 2003

• 한국재료학회:학술대회논문집
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• 한국재료학회 2004년도 춘계학술발표대회 및 제6회 신소재 심포지엄
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• pp.49-49
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• 2004

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2018년도 추계학술논문요약집
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• pp.295-296
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• 2018

• 한국결정성장학회:학술대회논문집
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• 한국결정성장학회 1997년도 Proceedings of the 12th KACG Technical Meeting and the 4th Korea-Japan EMGS (Electronic Materials Growth Symposium)
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• pp.19-22
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• 1997

The surface modificaion of alumina by $Al_2$O$_3$/SiC nanocomposite coating was studied in terms of processing and microstructure. A powder slurry of 5 vol% SiC composition was dipcoated onto presintered alumina bodies and pressurelessly sintered at 1$700^{\circ}C$ for 2 h in $N_2$. The used of organic binder and plasticizer in the slurry preparation, and the control of the density of presintered alumina body were found to be necessary to avoid cracking and warping during processing. The nanocomposite coating well bonded to the alumina body with thickness about 110 ${\mu}{\textrm}{m}$. The average grain size of coating (2 ${\mu}{\textrm}{m}$) was much finer than that of alumina body (13 ${\mu}{\textrm}{m}$). Fracture surface observations revealed mostly transgranular fracture for the coating, whereas intergranular fracture for the alumina body. Some pores (about 6%) were observed in the coating layer, although the alumina body showed fully dense microstructure.

• 한국세라믹학회지
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• 제16권3호
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• pp.155-163
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• 1979

This study was to explore the characteristics of 6 mole% CaO stabilized $ZrO_2$ prepared by wet chemical methods. The results of the experiments were as follows: 1. The powder calcined at 1000$^{\circ}$-110$0^{\circ}C$ was partly agglomerated. The morphology of agglomerate was spherical of 0.5-1$\mu{m}$ in size for Hot Petroleum Drying Method, chain-like of 1-2$\mu{m}$ for Freeze Drying Method, and irreqular of 2-3$\mu{m}$ for Coprecipitation Method. 2. Optimum calcining conditions for powder prepared by wet chemical methods were found: 110$0^{\circ}C$, 2h in air for Hot Petroleum Drying Method and Freeze Drying Method, and 100$0^{\circ}C$, 2h in air for Coprecipitation Method. 3. When specimen was calcined at 1000$^{\circ}$-110$0^{\circ}C$ in air for 2h and then sintered at 1$600^{\circ}C$ in air for 4h, the specimens prepared by wet chemical methods showed a high sintered density (94% of theoretical density) and a low open porosity (<0.8%); however, the sintered density of the specimen prepared by Oxide Wet Mixing Method was 90%. 4. The amount of cubic phase of sintered body prepared by wet chemical methods was observed to be higher than the one prepared by Oxide Wet Mixing Method. 5. It was found that Hot petroleum Drying Method, Freeze Drying Method and Coprecipitation Method were nearly the same in respect of the results of stabilization grade and sintered density of CaO-stabilized $ZrO_2$.

• 한국해양공학회지
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• 제20권5호
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• pp.77-81
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• 2006

In this study, monolithic liquid phase sintered SiC (LPS-SiC) was made by the hot pressing method with nano-SiC powder, whose particle size is 30 nm and less on the average. Alumina ($Al_{2}O_{3}$), yttria ($Y_{2}O_{3}$), and silica ($S_{i}O_{2}$) were used for sintering additives. To investigate the effects of $S_{i}O_{2}$, the $Al_{2}O_{3}/Y_{2}O_{3}$ composition was fixed and the ratio of $S_{i}O_{2}$ was changed, with seven different ratios tested. And to investigate the effects of the sintering temperature, the sintering temperature was changed, with $1760^{\circ}C,\;1780_{\circ}C$, and $1800_{\circ}C$ being used with a $S_{i}O_{2}$ ratio of 3 wt%. The materials were sintered for 1 hour at $1760^{\circ}C,\;1780^{\circ}C$ and $1800^{\circ}C$ under a pressure of 20 MPa. The effects on sintering from the sintering system used, as well as from the composition of the sintering additives, were investigated by density measurements. Mechanical properties, such as flexural strength, were investigated to ensure the optimum conditions for a matrix of SiCf/SiC composites. Sintered densityand the flexural strength of fabricated LPS-SiC increased with an increase in sintering temperature. Particularly, the relative density of a sintered body at $1800^{\circ}C$ with a non-content of $S_{i}O_{2}$, a specimen of AYSO-1800, was 95%. Also, flexural strength was about 750MPa.