• 자원리싸이클링
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• 제5권3호
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• pp.50-55
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• 1996

CaO를 $HNO_3$로 용해하여 제조한 (NO$Ca_3$)$_2$용액을 $NH_4$OH로 pH를 조절하고, 상압하의 온도에서 (NH$_4$)$_2$HPO$_4$를 주입시켜서 소정의 시간동안 Ca,,(PO$_4$),(OH)$_2$합성실험을 하였다. Ca,,(PO$_4$),(OH)$_2$는 pH 10~13 범위에서 생성되었고 이 HAP의 입경을 전자현미경으로 조사한 결과 0.1~0.5$mu extrm{m}$이었다. 반응온도는 $40~70^{\circ}C$, 결정화온도 $90^{\circ}C$이며 반응시간은 30분이 적당하였다. 생성된 Ca\ulcorner(PO$_4$)\ulcorner(OH)$_2$는 $500^{\circ}C$, 1시간동안 하소하여도 변화하지 않으나 80$0^{\circ}C$에서 1시간동안 하소한 시료는 $Ca_3$($PO_4$)$_2$와 HAP, CaO로 변화되었고, 구형의 미립자로 되어 있었다.

• 한국전자통신학회논문지
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• 제11권3호
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• pp.293-302
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• 2016

본 논문에서는 전이규칙이 모두 102인 Uniform CA(Uniform Cellular Automata, UCA) $\mathbb{C}_u$와 특성다항식이 $(x+1)^m$인 m-셀 90/150 hybrid CA $\mathbb{C}_h$를 합성한 CA의 특성을 분석한다. 먼저 $\mathbb{C}_u$로부터 유도된 여원 그룹 CA의 사이클 구조를 분석하고 이를 통해 모든 사이클의 길이가 같아지는 여원 CA의 조건을 제시한다. 그리고 $\mathbb{C}_u$와 $\mathbb{C}_h$를 합성한 CA $\mathbb{C}$의 최소다항식이 $(x+1)^q$일 때 $(T+I)^{q-1}F{\neq}0$을 만족하는 F를 여원벡터로 택하여 구성한 여원 그룹 CA $\mathbb{C}^{\prime}$의 사이클 구조를 분석한다.

• 한국세라믹학회지
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• 제21권2호
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• pp.113-120
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• 1984

In this study a comparative investigation for the effect of $K_2SO_4$ and $CaSO_4$ on the decomposition of $C_3S$ was made. When pure $C_3S$ which was synthesized in the laboratory was mixed with $K_2SO_4$ and oxides such as MgO $Al_2O_3$ and $Fe_2O_3$ and then reburned at the temperature range between 135$0^{\circ}C$ and 145$0^{\circ}C$ no decompo-sition occurred, But when $CaSO_4$ and $Fe_2O_3$ were added to $C_3S$ and then reburned at below 130$0^{\circ}C$ $C_3S$ was partly decomposed to $C_2S$and CaO composing $2C_2S$.$CaSO_4$ When $CaSO_4$ and $Al_2O_3$were added $C_3S$ was entirely decomposed to $C_2S$ and CaO at 1300~140$0^{\circ}C$ but it was not decomposed at 145$0^{\circ}C$.

• 한국세라믹학회지
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• 제30권7호
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• pp.527-534
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• 1993

The phenomena that excess sulfate hindred the C3S formation in the presence of clinker liquid phase were investigated. In the case of (NH4)2SO4, assuming SO3 atmospheric condition, sulfate stabilized C2S and was enriched at the surface of C2S grains, so C2S was prevented from being dissolved into clinker melt. CaSO4 showed the similar aspect with (NH4)2SO4, however, the prevention of C3S formation by CaSO4 took more influence that C2AS and C4A3 were formed below 100$0^{\circ}C$, and remained upto clinkering temperature, 145$0^{\circ}C$, thus these intermediate phases caught CaO which would participate the C3S formation.

• 자원리싸이클링
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• 제4권1호
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• pp.38-45
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• 1995

본 연구는 2.$0^{\circ}C$~85.3$^{\circ}C$, 2$\times$10\ulcornerM의 상압에서 탄산칼슘의 동질이상인 calcite, aragonite, vaterite의 생성과 그 형상에 미치는 온도의 영향을 조사한 것이다. 실험된 반응은 \circled1 Ca($HCO_3$)$_2$-Air bubble, \circled2 (OH)$Ca_2$ $-CO_2$, \circled3 (OH)$Ca_2$ $-H _2$$CO_3$, \circled4 $Ca(OH)_2$$-Na_2$CO$_3$, \circled5 $Ca(OH)_2$ $-K_2$ $ CO_3$, \circled6 $Ca(OH)_2$-($NH_4$)$_2$$CO_3$, \circled7 $CaCl_2$ $-Na2$ $CO_3$, \circled8 $CaCl_2$-K$_2$$CO_3$, \circled9 $CaCl_2$-($NH_4$)$_2$$CO_3$, \circled10 Ca($NO_3$)$_2$- $Na_2$$CO_3$, ⑪ Ca($NO_3$)$_2$- $K_2$$CO_3$, ⑫ Ca($NO_3$)$_2$등 12가지이며, 얻어진 실험결과는 아래와 같다. calcite는 반응종류에 상관없이 실험된 거의 모든 온도범위($2.0^{\circ}C$~$80.0^{\circ}C$)에서 생성하며 그 생성수율은 3$0^{\circ}C$정도일 때가 가장 높았다. aragonite는 반응에 따라 약간씩 차이는 있지만 주로 41.$0^{\circ}C$~53.$0^{\circ}C$ 사이에서 생성하기 시작하며 온도는 높을수록 그 수율은 높아진다. pH 또한 aragonite의 생성수율에 영향을 미치며 반응후 모액의 pH가 10.0~11.0 사이일 경우 생성수율이 최대가 되며 12.3 이상인 경우는 aragonite가 거의 생성되지 않았다. vaterite는 4$0^{\circ}C$ 이하에서만 생성하며 상당히 불안정하기 때문에 생성후 모액속에 방치할 경우 Cl￣를 포함하지않는 반응계에서는 10~60분 경과후 완전히 calcite로 전이하고 Cl￣를 포함하는 계에서는 약 140시간만에 완전히 calcite로 전이한다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2003년도 하계학술대회 논문집 Vol.4 No.1
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• pp.139-142
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• 2003

Microwave dielectric properties of $Ca(Li_{1/4}Nb_{3/4})O_3-CaTiO_3$ ceramic systems were investigated with calcination temperatures and amounts of $CaTiO_3$ in the range of 0.2 to 0.4mol. $Ca(Li_{1/4}Nb_{3/4})O_3$ ceramics having orthorhombic crystal structure could be synthesized at $750^{\circ}C$ and sintered well at $1250^{\circ}C$. They showed the dielectric constant of 26, quality factor($Q{\times}f_o$) of 13,000 and temperature coefficient of resonant frequency(${\tau}_f$) of $-49{\pm}2ppm/^{\circ}C$ With adding the $CaTiO_3$ amount the dielectric constant and ${\tau}_f$ increased due to the solute of $CaTiO_3$ but the quality factor decreased. The 0.7$Ca(Li_{1/4}Nb_{3/4})O_3-0.3CaTiO_3$ ceramic showed the dielectric constant of 44, quality factor($Q{\times}f_o$) of 12,000 and ${\tau}_f$ of $-9{\pm}1ppm/^{\circ}C$.

• 한국재료학회지
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• 제13권4호
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• pp.246-250
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• 2003

Calcium phosphate was prepared by chemical reaction formula using Oyster shells and $H_3$$PO_4$solutions. After added to 0.1 M∼0.9$ M H_3$$PO_4$ solution for oyster shell, prepared powders were investigated for heating properties and formation phase with heat treatment temperatures. As the results of XRD analysis of heated powders at $500^{\circ}C$∼$1200^{\circ}C$,$ CaCO_3$ phases were observed at the temperature of below 900 TEX>$^{\circ}C$ and in the condition of 0.1 M∼0.9 M $H_3$$PO_4$ solutions. However, $CaCO_3$, $CaPO_3$(OH) and $Ca_3$($PO_4$)$_2$ phases were appeared at the temperature range between $500∼900^{\circ}C$ and in the solution of 0.7 M to 0.9 M $H_3$$PO_4$. $Ca_{ 5}$($PO_4$)$_3$(OH) and CaO phases due to the decarbonation of oyster shells($CaCO_3$) were appeared at above $1000^{\circ}C$ and in the solution of below 0.5 M $H_3$X$PO_4$. However in the case of above 0.7 M $H_3$$H_4$ solutions, $Ca_{5}$ ($PO_4$)$_3$(OH) was decomposed into $Ca_3$($PO_4$)$_2$ at more higher 100$0^{\circ}C$. Thus $Ca_3$(X$Ca_4$)$_2$ phases were appeared at higher than 100$0^{\circ}C$.

• 한국재료학회지
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• 제7권3호
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• pp.180-187
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• 1997

평판형 고체산화물 연료전지용 연결재료로 사용되는 $La_{0.68}Ca_{0.32}Cr_{0.97}O_{3}$박막의 소결조건을 변화시키며 곡강도, 상대밀도 및 전기전도도를 측정하였다. 그 결과 $La_{0.68}Ca_{0.32}Cr_{0.97}O_{3}$의 곡강도는 소결온도와 소결시간이 증가할수록 증가하였고, 상대밀도는 $1400^{\circ}C$, 5시간이상 소결한 시편에서 94%이상을 얻었다. $La_{0.68}Ca_{0.32}Cr_{0.97}O_{3}$의 저온소결은 $Ca_{m}(C_{r}O_{4})_{n}$에 의해 이루어졌음이 관찰되었다. 또한 $La_{0.68}Ca_{0.32}Cr_{0.97}O_{3}$의 전기전도도는 $1400^{\circ}C$, 7시간 소결한 시편의 경우 $1000^{\circ}C$에서 약 100/cm이상을 얻었다.

• 한국세라믹학회지
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• 제34권11호
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• pp.1182-1186
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• 1997

La0.8Ca0.2Cr0.98O3 powder was prepared using the modified Pechini process. Various crystalline phases formed during thermal decomposition were investigated. (La,Ca)CrO4 phase, first formed from the precursor, was transformed to (La,Ca)CrO3 and CaCrO4 above 80$0^{\circ}C$, which remained up to 110$0^{\circ}C$. However, only (La,Ca)CrO3 phase consisting of orthorhombic and intermediate rhombohedral polymorphs was observed after sintering at 125$0^{\circ}C$. The specimens sintered at 140$0^{\circ}C$ exhibited 98% of relative density and rather wide grain size distribution with average grain size of 3-4 ${\mu}{\textrm}{m}$. Densification and grain growth of the specimens observed above 125$0^{\circ}C$ were presumably attributed to liquid phase sintering resulted from melting of Ca3(CrO4)2 phase.

• The Korean Journal of Physiology and Pharmacology
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• 제18권3호
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• pp.241-247
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• 2014

To investigate the underlying mechanisms of C18 fatty acids (stearic acid, oleic acid, linoleic acid and ${\alpha}$-linolenic acid) on mast cells, we measured the effect of C18 fatty acids on intracellular $Ca^{2+}$ mobilization and histamine release in RBL-2H3 mast cells. Stearic acid rapidly increased initial peak of intracellular $Ca^{2+}$ mobilization, whereas linoleic acid and ${\alpha}$-linolenic acid gradually increased this mobilization. In the absence of extracellular $Ca^{2+}$, stearic acid ($100{\mu}M$) did not cause any increase of intracellular $Ca^{2+}$ mobilization. Both linoleic acid and ${\alpha}$-linolenic acid increased intracellular $Ca^{2+}$ mobilization, but the increase was smaller than that in the presence of extracellular $Ca^{2+}$. These results suggest that C18 fatty acid-induced intracellular $Ca^{2+}$ mobilization is mainly dependent on extracellular $Ca^{2+}$ influx. Verapamil dose-dependently inhibited stearic acid-induced intracellular $Ca^{2+}$ mobilization, but did not affect both linoleic acid- and ${\alpha}$-linolenic acid-induced intracellular $Ca^{2+}$ mobilization. These data suggest that the underlying mechanism of stearic acid, linoleic acid and ${\alpha}$-linolenic acid on intracellular $Ca^{2+}$ mobilization may differ. Linoleic acid and ${\alpha}$-linolenic acid significantly increased histamine release. Linoleic acid (C18:2: ${\omega}$-6)-induced intracellular $Ca^{2+}$ mobilization and histamine release were more prominent than ${\alpha}$-linolenic acid (C18:3: ${\omega}$-3). These data support the view that the intake of more ${\alpha}$-linolenic acid than linoleic acid is useful in preventing inflammation.