• 제목/요약/키워드: CA3

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CAS계 유리가 첨가된 CaCO3-Al2O3 혼합물 및 화합물의 저온 소결 및 유전 특성 (Low Temperature Sintering and Dielectric Properties of CaCO3-Al2O3 Mixture and Compound with CAS-based Glass)

  • 윤상옥;김명수;김관수
    • 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.

국내산 함바나듐 티탄자철광으로부터 CaO 배소를 통한 바나듐 침출거동 (Vanadium Leaching Behavior from Domestic Vanadium Bearing Titanomagnetite Ore through CaO Roasting)

  • 신동주;주성호;이동석;전호석;신선명
    • 자원리싸이클링
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    • 제30권4호
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    • pp.27-34
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    • 2021
  • 본 연구에서는 국내산 함바나듐 티탄자철광으로부터 CaO 염배소 및 황산 침출을 통해 바나듐의 침출거동에 대해 고찰하였다. CaO의 첨가량 및 배소 온도에 따라 상의 변화를 살펴보았다. 배소 조건에 관계없이 Perovskite (CaTiO3)가 형성되었으며, CaO 함량이 높아지면 Calcium ferrite (CaFeOx) 상이 CaO 함량이 낮아지면 Hematite (Fe2O3)가 형성이 되었다. CaO 배소 후 1M 황산, 50℃, 고액비 10%에서 6시간 동안 침출을 진행하였다. 침출 결과 배소 시료의 형태가 소결일 경우 바나듐의 산화가 충분히 이루어지지 못해 침출률이 감소하였다. 또한 배소 온도가 낮으면 미 반응한 잔류 CaO의 영향으로 바나듐의 침출률이 감소하였다. 함바나듐 티탄자철광의 철과 티타늄의 침출률을 낮추기 위해서는 CaO의 첨가량을 최소화하여 CaTiO3와 CaFeOx의 형성을 억제할 필요가 있었다. 결과적으로 1150℃, 10 wt.% CaO 배소 산물을 침출하였을 때 86%의 바나듐, 4.3%의 철, 6.5%의 티타늄의 침출률을 얻을 수 있었다.

Mg-11Li-3Zn-1Sn-0.4Mn 마그네슘 합금의 Ca 첨가에 따른 미세조직 및 기계적 특성평가 (Effect of Ca Addtion on Microstructure and Mechanical Properties of Mg-11Li-3Zn-1Sn-0.4Mn Based Alloys)

  • 김정한;김용호;유효상;손현택;이성희
    • 한국재료학회지
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    • 제25권6호
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    • pp.269-273
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    • 2015
  • The effect of adding Ca on the microstructural and mechanical properties of as-cast Mg-11Li-3Zn-1Sn(wt%) alloys were investigated. Mg-11Li-3Zn-1Sn-0.4Mn with different Ca additions (0.4, 0.8, 1.2 wt%) were cast under an $SF_6$ and $Co_2$ atmosphere at $720^{\circ}C$. The cast billets were homogenized at $400^{\circ}C$ for 12h and extruded at $200^{\circ}C$. The microstructural and mechanical properties were analyzed by OM, XRD, SEM, and tensile tests. The addition of Ca to the Mg-11Li-3Zn-1Sn-0.4Mn alloy resulted in the formation of $Ca_2Mg_6Zn_3$, MgSnCa intermetallic compound. By increasing Ca addition, the volume fraction and size of $Ca_2Mg_6Zn_3$ with needle shape were increased. This $Ca_2Mg_6Zn_3$ intermetallic compound was elongated to the extrusion direction and refined to fine particles due to severe deformation during hot extrusion. The elongation of the 0.8 wt% Ca containing alloy improved remarkably without reduction strength due to the formation of fine grain and $Ca_2Mg_6Zn_3$ intermetallic compounds by Ca addition. It is probable that fine and homogeneous $Ca_2Mg_6Zn_3$ intermetallic compounds played a significant role in the increase of mechanical properties.

알루미나와 실리케이트 액상간의 반응에 따른 $CaO{\cdot}6Al_2O_3$ 상의 성장 및 용해 거동 (Growth and dissolution behavior of $CaO{\cdot}6Al_2O_3$ phase by reaction between alumina and silicate liquid phase)

  • 백용균;박상엽
    • 한국결정성장학회지
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    • 제5권3호
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    • pp.291-298
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    • 1995
  • 알루미나 고상소결체와 $CaMgSiO_4$간의 반응에 따른 반응상들의 성장 및 용해 거동을 $1600^{\circ}C$에서 열처리 시간을 변화하여 고찰하였다. 열처리시 알루미나는 $CaMgSiO_4$ 액상에 용융되어 중간에 반응상인 $CaO{\cdot}6Al_2O_3$와 최종 반응상인 $CaMgSiO_4$ 스피넬 형성이 관찰되었다. 중간상인$CaO{\cdot}6Al_2O_3$ 결정은 성장 모양과 용해 모양이 뚜렷하게 구분되었다.

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Effects of the Hinge Region of Cecropin A(1-8)-Melittin 2(1-12), a Synthetic Antimicrobial Peptide on Antibacterial, Antitumor, and Vesicle-Disrupting Activity

  • Shin, Song-Yub;Kang, Joo-Hyun;Jang, So-Yun;Kim, KiI-Lyong;Hahm, Kyung-Soo
    • BMB Reports
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    • 제32권6호
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    • pp.561-566
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    • 1999
  • CA(1-8)-ME(1-12) [CA-ME], composed of cecropin A(1-8) and melittin(1-12), is a synthetic antimicrobial peptide having potent antibacterial and antitumor activities with minimal hemolytic activity. In order to investigate the effects of the flexible hinge sequence, Gly-Ile-Gly, of CA-ME on antibiotic activity, CA-ME and three analogues, CA-ME1, CA-ME2, and CA-ME3, were synthesized. The Gly-Ile-Gly sequence of Ca-ME was deleted in CA-ME1 and replaced with Pro and Gly-Pro-Gly in CA-ME2 and CA-ME3, respectively. CA-ME1 and CA-ME3 showed a significant decrease in antitumor activity and phospholipid vesicle-disrupting ability. However, CA-ME2 showed similar antitumor and vesicle-disrupting activities, as compared with CA-ME. These results suggest that the flexibility or ${\beta}$-turn induced by Gly-Ile-Gly or Pro in the central part of CA-ME may be important in the electrostatic interaction of the N-terminus cationic ${\alpha}$-helical region with the cell membrane surface and the hydrophobic interaction of the C-terminus amphipathic ${\alpha}$-helical region with the hydrophobic acyl chains in the cell membrane. CA-ME3 exhibited lower antitumor and vesicle-disrupting activities than CA-ME and CA-ME2. This result suggests that the excessive ${\beta}$-turn structure caused by the Gly-Pro-Gly sequence in CA-ME3 seems to interrupt ion channel/pore formation in the lipid bilayer. We concluded that the appropriate flexibility or bilayer. We concluded that the appropriate flexibility or ${\beta}$-turn structure provided by the central hinge is responsible for the effective antibiotic activity of the antimicrobial peptides with the helix-hinge-helix structure.

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CaTi$O_3$에서 양이온 비화학양론 (Cation Nonstoichiometry in CaTi$O_3$)

  • 한영호
    • 한국재료학회지
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    • 제2권3호
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    • pp.207-212
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    • 1992
  • 과잉의 CaO와 $TiO_2$를 각각 포함한 $CaTiO_3$의 결함구조를 평형상태의 전기전도도를 $85O^{\circ}C$$1050^{\circ}C$사이에서 산소분압의 함수로 측정하여 연구하였다. 과잉의 CaO는 A site와 B site에 나누어져서 용해되어 $Ca_{Ti}$"와 Vo", 결함을 생성하였으며, 과잉의 $TiO_2$$V_{Ca}$"과 Vo"을 생성했다. 평형상태의 전기전도도는 CaO 용해도 5000ppm과 $TiO_2$ 용해도 2000ppm을 각각 나타냈다. 과잉의 양이온에 의하여 생성된 산소공공은 이온전도를 하여 넓은 영역의 산소 분압에 무관한 전도도 최소값을 보였으며, 반대로 대전된 음이온 결함과 결함쌍은 관찰되지 않았다.온 결함과 결함쌍은 관찰되지 않았다.

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아스파르트산 킬레이트 칼슘의 칼슘 결핍쥐에서의 생물학적 유용성 (Bioavailability of Aspartic Acid Chelated Calcium in Calcium Deficient Rats)

  • 박명규;하태열;신광순
    • Journal of Nutrition and Health
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    • 제44권6호
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    • pp.474-480
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    • 2011
  • Calcium (Ca) is an essential element to maintain body homeostasis. However, many factors disturb calcium absorption. Aspartic acid chelated calcium (AAC) was synthesized by new methods using calcium carbonate and aspartic acid. This study was carried out to investigate the bioavailability of AAC in Ca-deficient rats. The experimental groups were as follows: NC; normal diet control group, CD-C; untreated control group of Ca-deficient (CD) rats, CD-$CaCO_3$; $CaCO_3$ treated group of CD rats, CD-AAC; AAC treated group of CD rats, and CD-SWC; and seaweed-derived Ca treated group of CD rats. The Ca content of various types of Ca was held constant at 32 mg/day, and the four CD groups were fed for 7 days after randomized grouping. Ca content in serum, urine, and feces within feeding periods were analyzed to confirm Ca absorption. Serum Ca content was significantly higher in the CD-AAC (11.24 mg/dL) and CD-SWC (10.12 mg/dL) groups than that in the CD-C (8.6 mg/dL) group 2 hours following the first administration. The Ca content in feces was significantly lower in the CD-AAC (35.4 mg/3 days) and CD-SWC (71.1 mg/3 day) groups than that in the CD-$CaCO_3$ (98.7 mg/3 days) group (p > 0.05). AAC had a 2.3-fold higher absorption rate of Ca than that of SWC. No differences in fibula length were observed in the NC and CD groups. The fibula weights of the CD-AAC (0.33 g) and CD-SWC (0.33 g) groups increased compared to those in the CD-C (0.27 g) group; however, no significant difference was observed between the CD groups. We conclude that bioavailability of AAC is higher than that of seaweed-derived Ca or inorganic Ca. Thus, these findings suggest the AAC has potential as a functional food material related to Ca metabolism.

$Cr_2$$O_3$가 첨가된 $CaMnO_3$-$CaTiO_3$계 페로브스카이트 써미스터의 전기적 특성 (Electrical Properlies of $Cr_2$$O_3$ Added $CaMnO_3$-$CaTiO_3$ Perovskite Thermistor)

  • 양기호;윤상옥;윤종훈;장성식
    • 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.

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생활쓰레기 소각(燒却)비산재로부터 $CaCO_3$ 제조(製造)에 관한 연구(硏究) (Study on $CaCO_3$ Preparation from MSWI Fly Ash)

  • 최우진;박은규
    • 자원리싸이클링
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    • 제15권5호
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    • pp.47-51
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    • 2006
  • 국내 생활쓰레기 소각시설에서 발생되는 소각재의 양은 2005년 경우 약 420,000톤에 달하고 있으며, 그중 비산재 발생량은 약 68,000톤에 달하고 있다. 비산재는 지정폐기물로 분류되어 일반적으로 고형화 및 안정화 처리 후 매립되고 있으며, 단지 발생량의 약 20%만이 재활용되고 있다. 비산재의 경우 CaO의 함량이 50%까지 이르고 있으며, 그 이유는 배가스 처리시 CaO를 기본으로 하는 물질을 다량으로 사용하기 때문이다. 본 연구에서는 비산재에 함유되어 있는 CaO를 회수하여 $CaCO_3$ 분말을 제조하기 위한 기초실험을 수행하였다. CaO를 선택적으로 용해하기 위하여 설탕용액을 사용하였으며, 기초 실험결과에 의하면 CaO용해를 위한 최적조건은 비산재 농도 10%, 반응시간 15분, 설탕농도 $10{\sim}15%$ 및 적정 pH는 $10.5{\sim}11$로 나타났다. $CaCO_3$ 분말은 회수된 CaO 용해액에 $CO_2$가스를 주입시켜 제조하였으며 회수된 $CaCO_3$ 백색도는 매우 우수한 것으로 조사되었다.

동축형 공진기용 $(PbCa)ZrO_3$ 분말의 합성 (Preparation of Fine-particle $(PbCa)ZrO_3$ for Resonator)

  • 이병하;이경희;윤성화
    • 한국세라믹학회지
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    • 제30권8호
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    • pp.635-642
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    • 1993
  • To obtain a higher dielectric constant material, we investigated Ca substitution for Pb in PbZrO3. In this study, the four mixtures of (Pb0.68Ca0.32)ZrO3, (Pb0.65Ca0.37)ZrO3, (Pb0.63Ca0.37)ZrO3, and (Pb0.60Ca0.40)ZrO3 were prepared by coprecipitation reaction of Pb(NO3)2, ZrOCl2, and CaCl2 with (NH4)2CO3 and NH4OH in aqueous solution. The (Pb1-xCax)ZrO3 with different x mole fractions (x=0.35, 0.37) showed not only high dielectric constant, but also high Q values and low temperature coefficient of the capacitance.

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