• 한국결정성장학회지
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• 제2권2호
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• pp.20-32
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• 1992

$Na_2O-CaO-MgO-Al_2O_3-SiO_2$계를 기본조성으로 하여 $Na_2O$에 $Li_2O 0.05wt%, $K_2O$를, CaO에 MgO 12.0wt%, ZnO 6.0%를 각각 치환하여 조성을 선정하였다. 기본 유리조성의 결정상은 wollastonite이고, 치환된 조성들은 diopside, diopside.tremolite의 혼정이 나타났다. $Na_2O$를 $Li_2O$로 치환한 시편은 열팽창계수가 감소하였지만 CaO를 ZnO로 치환한 시편은 열팽창 계수가 증가하였다. 곡강도에 있어서는 치환에 따라 모두 증가시켰다. 핵행성제로 $ZrO_2와 $CaF_2$를 각각 1~2wt%의 변화를 시켜본 결과 핵형성제 $ZnO_2$와 $CaF_2$가 1:1, 1:2인 시편은 $1000~1050^{\circ}C$온도에서 급격한 결정성장을 보였으며 1:2시편이 가장 낮은 열팽창 계수값을 나타냈다. 곡강도는 모두 $1000~1050^{\circ}C$의 결정화 온도 범위에서 높은 강도를 나타내었다. 결정화에 필요한 활성화 에너지는 Ozawa와 Kissinger식으로 plot하여 각각 55.24kcal/mol과 53.05kcal/mol이다.

• 한국재료학회지
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• 제13권9호
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• pp.572-580
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• 2003

Synthesizing behavior and microstructural evolution of $CaZrO_3$and $m-ZrO_2$in a thermal reaction process of $ZrSiO_4$-$xCaCO_3$mixtures, where x is 7 and 19, were investigated to determine the addition amount of CaO in CaO:$ZrO_2$:$SiO_2$ternary composition. CaZrO$_3$-Ca$_2$SiO$_4$precursor prepared by the mixture of $ZrSiO_4$and CaCO$_3$in aqueous suspending media was controlled to the acidic (pH=4.0) condition with HCI solution to enhance the thermal reaction. The addition amount of dispersant into the $ZrSiO_4$-$xCaCO_3$slip increased with increasing mole ratio of $CaCO_3$, which was associated with the viscosity of slip. Decarbonation reaction was activated with an increase of the addition amount of $CaCO_3$, showing different final temperatures in $ZrSiO_4$-$7CaCO_3$and $ZrSiO_4$-$19CaCO_3$mixtures as about 980 and 116$0^{\circ}C$, respectively, for finishing decarbonation reaction. The grain morphology was changed to spherical shape for all samples with an increase of sintering temperature. The grain size and phase composition of the synthesized composites depended on the mixture ratio of Zrsi04 and CacO3 powders, indicating that the main crystals were m-ZrO2 ($\leq$3 $\mu\textrm{m}$) and $CaZrO_3$ ($\leq$ 7 $\mu\textrm{m}$) in $ZrSiO_4$$>-7CaCO_3$and $ZrSiO_4$-$19CaCO_3$mixtures, respectively.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2000년도 하계학술대회 논문집
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• pp.399-402
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• 2000

For improvement of B constant in $CaMnO_3$-$CaTiO_3$ perovskite type thermistors, effect of $Cr_2$$O_3$ addition ranged from 0.0wt% to 5.0wt% on electrical properties were investigated with contents and sintering temperatures in the view of crystal and microstructures. The solubility limit of Cr$_2$O$_3$was up to 0.5wt% judging from the result of lattice parameter. The grain size was decreased and the resistance at room temperature and B constant were increased with the addition of $Cr_2$$O_3$.On particular, B constant of$CaMnO_{3-x}$$Cr_2$$O_3$ system was increased greatly from 1574k to 2598k at 0.5wt% $Cr_2$$O_3$addition. Further addition of $Cr_2$$O_3$, however, resulted in the decrease of the resistance and B constant due to the $Cr_2$$O_3$ precipitation on the grain boundary. As the$CaTiO_3$contents increased in the $CaMnO_3$-$CaTiO_3$ system, the resistance at room temperature and B constant were highly changed.

• 한국전기전자재료학회논문지
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• 제22권5호
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• pp.397-404
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• 2009

Effects of ceramic filler types and dose on the low temperature sintering and dielectric properties of ceramic/$CaO-Al_2O_3-SiO_2$ (CAS) glass composites were investigated. All of the specimens were sintered at $850{\sim}900^{\circ}C$ for 2 h, which conditions are required by the low-temperature co-firing ceramic (LTCC) technology. Ceramic fillers of $CaCO_3$, $Al_2O_3$, $CaCO_3-Al_2O_3$ mixture, and $CaCO_3-Al_2O_3$ compound ($CaAl_2O_4$), respectively, were used. The addition of $Al_2O_3$ yielded the crystalline phase of alumina, which was associated with the inhibition of sintering, while, $CaCO_3$ resulted in no apparent crystalline phase but the swelling was significant. The additions of $CaCO_3-Al_2O_3$ mixture and $CaAl_2O_4$, respectively, yielded the crystalline phases of alumina and anorthite, and the sintering properties of both composites increased with the increase of filler addition and the sintering temperature. In addition, the $CaAl_2O_4$/CAS glass composite, sintered at $900^{\circ}C$, demonstrated good microwave dielectric properties. In overall, all the investigated fillers of 10 wt% addition, except $CaCO_3$, yielded reasonable sintering (relative density, over 93 %) and low dielectric constant (less than 5.5), demonstrating the feasibility of the investigated composites for the application of the LTCC substrate materials.

• 한국세라믹학회지
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• 제29권5호
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• pp.341-346
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• 1992

The effects of CaO addition on the low temperature degradation behavior of 2.5Y-TZP ceramics were investigated. Y2O3-CaO-ZrO2 ceramics were prepared from the commercial Y-TZP powder added within 1 mol% of CaO. Fully tetragonal phase could be obtained at each composition under sintering condition of 1500$^{\circ}C$ for 1 hour. As the amount of CaO increased, grain size was decreased. From the result of heat treatment at 200$^{\circ}C$, volume fraction of monoclinic phase formed on the surface of each specimen was decreased with higher CaO amount. Stability of tetragonal ZrO2 phase for low temperature heat treatment was increased by CaO addition without the degradation of mechanical properties.

• 한국주조공학회지
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• 제26권3호
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• pp.146-151
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• 2006

In this study, effects of CaD and Ca addtions on microstructure and ignition resistance of pure Mg were investigated. With increasing Ca and CaO contents, the grains in Ca and CaO added Mg were refined and ignition temperatures of CaO and Ca added Mg increased, too. As a result of phase analysis, CaO seemed to be reduced to Ca. $Mg_2Ca$ phase was formed even in 0.1 wt%CaO added pure Mg by reduction mechanism, while $Mg_2Ca$ phase was formed in over 1.35 wt% Ca added pure Mg. Thermodynamical consideration for the reduction mechanism of CaO in pure Mg was carried out.

• 한국세라믹학회지
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• 제33권5호
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• pp.563-571
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• 1996

In order to fabricate solid electrolyte CaO-stabilized ZrO2 of high density sintered body economically 13 mol% CaO-stabilized ZrO2 powders were synthesized by the coprecipitation method. The characteristics and sintering behavior of fine powder were investigated. The precipitates has the specific surface area of 193 m2/g and apperaed to be fine and spherical primary particles with a size of approximately 5nm. The crystalliza-tion temperture of CaO-stabilized ZrO2 was 462$^{\circ}C$. The tetragonal phase was stable in the low calcining tempe-rature regions and the cubic zirconia solid solution was formed from above 120$0^{\circ}C$ through an intermediate stage of formation of CaZrO3 By introducing fine powders washed with alcohol and ball-milling process after calcination the sintered body was possible to attain the value of above 92% of the theoretical density at low temperature of 120$0^{\circ}C$.

• 유기물자원화
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• 제29권4호
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• pp.41-46
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• 2021

초음파/과산화칼슘 처리(US/CaO₂)에 따른 하수슬러지의 가용화 정도를 확인하고자 과산화칼슘의 주입량(0.01, 0.02, 0.03, 0.04 및 0.05 g CaO₂/g VSS)에 따른 처리 효율을 비교하였다. 가용화의 주요 지표인 VSS 감량화율, 가용화율, SCOD/VSS, SCOD 증가속도 및 미생물의 세포벽이 파쇄되었는지 확인하기 위하여 LB-EPS와 TB-EPS를 측정하였다. 실험결과, US/CaO₂(0.05 g CaO₂/g VSS) 조건에서 가용화율은 50.7%로 US 처리(23.4%)보다 높은 효율을 나타내었으며, VSS 감량화율도 US/CaO₂(0.05 g CaO₂/g VSS) 조건에서 17.7%, US 조건에서는 7.1%로 가용화율과 유사한 경향을 나타내었다. 조사시간 10분부터 90분까지 SCOD의 증가속도는 US/CaO₂(0.02 g CaO₂/g VSS) 조건에서 0.0151 min^-1으로 가장 빠른 속도를 나타내었다. TB-EPS는 US/CaO₂(0.05 g CaO₂/g VSS)조건에서 59.0%, US 조건에서 36.4% 감소하였다. TB-EPS는 초기 10분동안 빠르게 감소하였으며, 이후부터 상대적으로 완만하게 줄어드는 것을 확인할 수 있었다. 과산화칼슘의 주입량에 따른 TB-EPS의 감소량은 큰 차이가 없는 것으로 나타났다.

• 한국재료학회지
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• 제6권7호
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• pp.684-691
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• 1996

Bi-계 고온초전도체인 Bi2Sr2Ca2Cu3O10(Bi-2223)단일상을 반응시간을 줄이면서 합성하기 위하여 Bi-Sr-Ca-Cu-O계 내에 존재하는 Bi2Sr2Ca2Cu3O10(Bi-22o1), Bi2Sr2Ca2Cu3O10(Bi-2212), (Ca0.91Sr0.09)-CuO2의 혼합물, 특히 정확한 Bi1.7Pb0.4Sr2Ca2Cu3O10+x의 조성대신 (Ca0.91Sr0.09)CuO2가 많이 첨가된 조성의 혼합물에서 Bi-2223가 가장 쉽게 형성되었다. Bi-2223상은 86$0^{\circ}C$와 87$0^{\circ}C$에서 60시간 이내에 형성되었다. 소량의 Bi-2212상은 장시간의 반응후에도 여전히 존재하였다. 중간화합물을 이용한 합성방법이 통상의 소결방법에 비해 반응시간내에 소량의 불순물상들을 가진 Bi-2223상을 형성시킬 수 있다.

• 대한화학회지
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• 제46권4호
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• pp.336-345
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• 2002

본 연구에서는 조합화학을 이용하여 $CaO-Gd_2O_3-Al_2O_3$계에서 $Eu^{3+}$와 $Tb^{3+}$활성 적색 및 녹색 PDP용 형광체를 탐색하였으며 탐색된 형광체의 합성온도, 최적조성,발광 특성 등을 조사하였다. $CaO-Gd_2O_3-Al_2O_3$의 삼성분계의 형광특성 라이브러리를 작성하기 위하여 210개의 다른 조성을 가진 시료를 고분자 착체 중합법으로 합성하였다. 합성된 형광체 분말을 VUV PL로 측정하여 형광 특성 라이브러리를 작성하였고 발광특성이 잘 나타난 시료를 XPD를 이용하여 결정 구조를 확인하였다. 적색 형광체로서 탐색된 $Ca_{\alpha}$G$d_{0.95-\alpha-\beta}$$Al_\beta$$O_\delta$ : Eu(0.02< $\alpha+\beta$ <0.04)형광체는 색순도 면에서 상용형광체보다 개선된 특성을 보였으며 녹색 형광체로서 탐색된 $CaGdAl_3O_7$ : Tb, Ca$Al_{12}$$O_{19}$ : Tb, $Gd_4Al_2$$O_9$ : Tb, $Gd_3Al_5$$O_{12}$ : Tb 형광체 중에서 $CaGdAl_3O_7$ : Tb, Ca$Al_{12}$$O_{19}$ : Tb형광체는 상용 형광체에 비해 잔광시간이 짧은 특성을 보였다