• 한국세라믹학회지
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• 제41권8호
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• pp.567-572
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• 2004

The variation of the sintered density and grain size of UO$_2$ as a function of the Li$_2$O amount and sintering atmosphere was observed. Li$_2$O enhanced the grain growth of the UO$_2$ pellet in H$_2$, but rather hindered it in $CO_2$ atmosphere. Grain size of the UO$_2$ and UO$_2$-0.1 wt%Li$_2$O pellets was, respectively, 8 $\mu$m and 100 $\mu$m at 168$0^{\circ}C$ in the H$_2$ atmosphere, and that of each pellet was, respectively, 24 $\mu$m and 17 $\mu$m at the same temperature in the $CO_2$ atmosphere. As-received Li$_2$O powder, which had been composed of Li$_2$O and LiOH, was converted to the Li$_2$CO$_3$ phase after heating to 80$0^{\circ}C$ in $CO_2$. On the other hand, the Li$_2$O and LiOH phases remained unchanged in H$_2$ atmosphere. In the H$_2$, the as-received Li$_2$O powder began to evaporate at about 105$0^{\circ}C$ and then about 20 wt% residue was left at 150$0^{\circ}C$. But, most of the Li elements evaporated at 150$0^{\circ}C$ in the $CO_2$ atmosphere.

• 한국세라믹학회지
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• 제50권3호
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• pp.218-225
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• 2013

The densification behavior and strength of sintered reaction bonded silicon nitrides (SRBSN) that contain $Lu_2O_3-SiO_2$ additives were improved by the addition of fine Si powder. Dense specimens (relative density: 99.5%) were obtained by gas-pressure sintering (GPS) at $1850^{\circ}C$ through the addition of fine Si. In contrast, the densification of conventional specimens did not complete at $1950^{\circ}C$. The fine Si decreased the onset temperature of shrinkage and increased the shrinkage rate because the additive helped the compaction of green bodies and induced the formation of fine $Si_3N_4$ particles after nitridation and sintering at and above $1600^{\circ}C$. The amount of residual $SiO_2$ within the specimens was not strongly affected by adding fine Si powder because most of the $SiO_2$ layer that had formed on the fine Si particles decomposed during nitridation. The maximum strength and fracture toughness of the specimens were 991 MPa and $8.0MPa{\cdot}m^{1/2}$, respectively.

• 한국세라믹학회지
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• 제11권1호
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• pp.29-35
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• 1974

Effect of calcium sulfate and barium sulfate on the formation of portland cement clinker was studied by means of chemical analysis. DTA and X-ray diffraction analysis. In the presence of liquid phase, effect of the additives on the formation of tricalcium silicate was examined according to the reaction, 2CaO.$SiO_3$＋CaO$\longrightarrow$3CaO.$SiO_3$, which is the principal reaction in portland cement clinkerization, and optimum conditions in firing clinker concerning amount of additive, firing time and temperature were determined, and its kinetics was referred to. The experimental results are summerized as follow: (1) Appropriate burning temperature range of cement clinker is more limited as the content of calcium sulfate in clinker is increased. Amount of calcium sulfate, firing time and temperature in proper condition of clinkerization is related to each others. Being added suitable quantity of calcium sulfate, firing temperature of clinker can be lowered about $100^{\circ}C$. (2) When 3-5 mole% of calcium sulfate is added, firing time of 15-30 minutes at about $1380^{\circ}C$ is reasonable, and if the content is over7 mole %, firing for 1 hr. or more at $1350^{\circ}C$ is anticipated to be optimum condition. (3) In the reaction of tricalcium silicate formation, the role of barium sulfate as a mineralizer is similar to that of calcium sulfate, but the optimum firing temperature of cement clinker containing barium sulfate tends to be 20-$30^{\circ}C$ higher than that of clinker containing calcium sulfate. (4) When barium sulfate is used as mineralizer, 2-3 mole % of it to tricalcium silicate is recommended and if it is added more than this amount, free CaO is increased rapidly in clinker and alite formation is inhibited.

• 한국세라믹학회지
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• 제46권2호
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• pp.123-130
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• 2009

To understand the formation of core-shell structure in $BaTiO_3$ (BT) grains in multilayer ceramic capacitors, specimens were prepared with BT powders mixed with Y and Mg, and their microstructures were investigated with scanning electron microscopy, x-ray diffractometry, and transmission electron microscopy. Microstructural investigation showed that Y dissolved easily in BT lattice to a certain depth inside of the grain, whereas Mg tended to stay at grain boundaries rather than become incorporated into BT. It was considered that in case of Y and Mg addition in a proper ratio, Y could play a dominant role in the formation of shell leading to a slight dissolution of Mg in the shell. Next, the effects of ball-milling conditions on the core-shell formation were studied. As the ball-milling time increased, the milled powders did not show a significant change in size distribution but rather an increase of residual strain, which was attributed to the milling damage. The increase in milling damage facilitated the shell formation, leading to the increased shell portion in the core-shell grain.

• 한국세라믹학회지
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• 제40권6호
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• pp.530-538
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• 2003

110 K 상의 산화물 고온초전도체를 B $i_{1.84}$P $b_{0.34}$S $r_{1.91}$C $a_{2.03}$C $u_{3.06}$ $O_{10+}$$\delta$의 출발조성비로 고상반응법에 의해 합성하였다. 합성된 Bi계 110 K 상의 산화물 고온초전도 물질을 다시 분말 상태로 만든 후, MgO 금속산화물 분말을 5~50 wt%의 각 비율로 혼합하였다. MgO 금속산화물 분말이 혼합된 시편들을 820~86$0^{\circ}C$로 24시간동안 최종 소결시켰다. 그 후, 각 시편들에 대하여 x-선, $T_{c}$, SEM 등을 측정하여 MgO 금속산화물 혼합량에 대한 초전도특성 및 표면의 입자 크기 변화 등에 대한 조사를 진행하였다. MgO 금속산화물의 혼합량이 증가됨에 따라 MgO 관련 피크들의 강도 및 2212 상들의 피크들의 비율은 증가되었고, 시편 내 2223 상의 비율은 감소하고 2212상의 비율은 증가되었다.다.은 증가되었다.다.

• 한국결정성장학회지
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• 제18권6호
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• pp.237-241
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• 2008

AlN 소결체를 제조함에 있어서 $Y_2O_3$를 소결 첨가제로 하여 일축 가압 소결법을 적용하여 소결 조제 첨가량의 변화와 소결 시간의 변화에 따른 소결 특성, 미세구조 및 열전도도 측성에 대하여 조사하였다. $Y_2O_3$의 첨가로 인하여 AlN의 치밀화가 첨가하지 않은 경우보다 증진됨을 확인할 수 있었으며, 결정립계 및 결정립계 삼중점에서 YAG 이차상을 형성함으로써 AlN 결정 격자 내의 산소 결함 농도를 낮춰 열전도도를 향상시킴을 알 수 있었다. 특히, 소결 시간을 증대함에 따라 결정립 성장 및 열전도도의 방해 요소인 YAG 이차상이 고온에서 휘발됨에 따라 열전도도가 크게 향상됨을 확인할 수 있었다.

• Journal of Periodontal and Implant Science
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• 제31권3호
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• pp.555-564
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• 2001

The purpose of this study is to evaluate the bioresorbability of Calcium Polyphosphate added with $Na_2O$ and chitosan. Though calcium phosphate ceramics meet some of the needs for bone replacement, they have some limitation of unresorbability and fibrous encapsulation without direct bone apposition during bone remodelling. To solve these problem, we developed a new ceramic, calcium polyphosphate(CPP), and report the biologic response to CPP in extraction sites of beagle dog. Porous CPP granules were prepared by condensation of anhydrous $Ca(H_2PO_4)_2$ to form non-crystalline $Ca(PO_3)_2$. CPP granules added with $Na_2O$ and chitosan were implanted in extraction sockets and histologic observation were performed at 12 weeks later. Histologic observation at 12 weeks revealed that CPP matrix were mingled with and directly apposed to new bone without any intervention of fibrous connective tissue. CPP granules added with chitosan were well adatped without any adverse tissue reaction and resorbed slowly and spontaneously. CPP granules added with $Na_2O$ and chitosan show multinucleated giant cells and osteoblast-like cells around grafted material and newly formed bone. This result revealed that CPP, regardless of its additive component, had a high affinity for bone and had been resorbed slowly. From this results, it was suggested that CPP is promising ceramic as a bone substitute and addition of $Na_2O$ and chitosan help biodegradation. In further study , it will be determined which concentration of $Na_2O$ help biodegradation and the other additive components increase the degradation rate.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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• pp.391.2-391.2
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• 2014

Solution-processible hybrid bipolar field effect transistors (HBFETs) with balanced hole and electron mobilities were fabricated using a combination of the organic p-type poly (3-hexylthiophene) (P3HT) layer and inorganic n-type ZnO material. The hole and electron mobilities were first optimized in single layer devices by using acetonitrile as a solvent additive to process the P3HT and annealing to process the ZnO layer. The highest hole mobility of the P3HT-only-devices with 5% acetonitrile was 0.15 cm2V-1s-1, while the largest electron mobility was observed in the ZnO-only-devices annealed at $200^{\circ}C$ and found to be $7.2{\times}10-2cm2V-1s-1$. The inorganic-organic HBFETs consisting of P3HT with 5% acetonitrile and ZnO layer annealed at $200^{\circ}C$ exhibited balanced hole and electron mobilities of $4.0{\times}10-2$ and $3.9{\times}10-2cm2V-1s-1$, respectively. The effect on surface morphology and crystallinity by adding acetonitrile and thermal annealing were investigated through X-ray diffraction and atomic force microscopy (AFM). Our findings indicate that techniques demonstrated herein are of great utility in improving the performance of inorganic-organic hybrid devices

• 자원리싸이클링
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• 제11권4호
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• pp.27-36
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• 2002

생활폐기물의 소각으로 발생되는 바닥재(bottom ash)로 calcium-chloroaluminate($l1CaOㆍ7Al_2$$O_3$ㆍ$CaCl_2$)가 함유된 클링커를 제조한 후 이들 클링커의 수화반응성 및 보통 포틀랜드 시멘트와 혼합 사용할 때의 압축강도 및 중금속 용출특성을 연구하였다. 시약으로 calcium-chloroaluminate를 제조한 결과. calcium-chloroaluminate는 80$0^{\circ}C$부터 생성되며, $CaSO_4$ 및 $Ca(OH)_2$ 와의 수화반응에 의해 ettringite($3CaOㆍAl_2$$O_3$ㆍ$3CaSO_4$ㆍ$32H_2$O)가 생성된다. 4 mesh 이하의 바닥재를 분쇄하지 않고 온도별로 1시간 소성한 결과, 80$0^{\circ}C$부터 calcium-chloroaluminate가 30 mesh 이하의 입도에서 합성되었다. $1,000^{\circ}C$에서 소성한 30 mesh 이하의 바닥재에 무수석고($CaSO_4$)를 10 : 6의 중량비로 혼합한 후 이들 혼합물을 보통 포틀랜드 시멘트에 3～13 wt.% 첨가하여 제조한 모르타르의 압축강도를 측정한 결과, 이들 혼합물의 치환량이 11 wt.%까지 증가됨에 따라 보통 포틀랜드 시멘트의 압축강도보다 높았다. 각 모르타르 공시체를 1 mm 이하로 분쇄하여 중금속 용출시험 결과, 용출된 중금속의 농도는 환경규제치보다 낮았다.

• 한국재료학회지
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• 제3권1호
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• pp.33-42
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• 1993

세라믹스를 공업분야에 응용범위를 확대하기 위한 최선의 수단으로 금속과의 복합화를 들수 있다. 금속과 복합화하는 방법중에서 세라믹스/금속접합은 부품의 제조등에 이용될 수 있는 수단으로 많은 연구가 행하여져서 이미 몇몇 부품에 대해서는 실용화가 되고 있고 현재에도 활발히 연구가 되고 있다. 따라서 본 연구에서는 여러가지 접합법중에서도 비교적 공정이 간편한 활성 브레이징법을 이용해 $Al_2$$O_3$ 와 304 스테인레스강을 접합하였으며 이때 삽입금속으로는 Cu-Ti합금을 사용하였고 접합온도 및 접합시간 범위는 각각 110$0^{\circ}C$-120$0^{\circ}C$, 0.5h-1.5h, 그리고 브레이징로 내의 분위기는 $10^{-3}$-$10^{-4}$ torr로 유지하였다. 접합후 접합부 조직에 대한 접합조건의 영향을 검토하고 반응생성물을 EDX, WDX 및 XRD을 이용해 분석하였으며 반응층형성을 위한 계면화학반응을 고찰하였다. 그 결과 알루미나와 삽입금속의 계면에서 접합을 유도하는 반응층은 T$i_2$$O_3$임을 확인할 수 있었다.