• 제목/요약/키워드: $CaO_2$

검색결과 4,355건 처리시간 0.027초

$CaO-P_2O_5-SiO_2$계 유리의 생체활성 (Bioactivity of $CaO-P_2O_5-SiO_2$ Glasses)

  • 조정식;김철영
    • 한국세라믹학회지
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    • 제30권6호
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    • pp.433-440
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    • 1993
  • The bioactivity of glasses in the CaO-SiO2 system and CaO-P2O5-SiO2 system with less than 10mol% of P2O5 was investigated by in vitro test in simulated body flood(SBF). The formation of Ca.P film and hydroxyapatite on the surface of glasses after in vitro test was analysed by X-ray photoelectron spectoscopy (XPS), fourier transform infrared reflection spectroscopy (FT-IRRS), energy dispersive X-ray spectroscopy (EDS), and scanning electron microscopy (SEM) observation. In the early stage of Ca.P film formation after in vitro test for CaO-SiO2 and CaO-P2O5-SiO2 glasses, the rate of Ca.P film formation on the surface of the glasses was dependent of structural parameter (Y) evaluated from the glass composition. First, in the case of the glasses having Y value below 2, Ca.P film and SiO2-rich layer were formed simultaneously, and there were no differences of the rate of Ca.P film formation in terms of the Y values. Second, in the case of the glasses having Y value above 2, the SiO2-rich layer was formed, and then Ca.P.Si mixed layer was formed in the silica gel structure of the SiO2-rich layer, and finally the Ca.P film on the surface of SiO2-rich layer. The rate of Ca.P film formation delayed as the Y values increased. The rate of hydroxyapatite formation of glasses (the rate of transformation from Ca.P film to hydroxyapatite) seems to be propotional to the rate of Ca.P film formation and Y value. The rate of hydroxyapatite formation of glasses belonging to the second group was delayed as structural parameter increased, and the hydroxyapatite crystal showed spherical growth in the early reaction stage, and then showed silkworm-like linear growth as the reaction time increased.

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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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$CaO-SiO_2-P_2O_5$계 바이오 시멘트 유리의 조성이 경화 및 Hydroxyapatite 형성에 미치는 영향 (Compositional Effects of $CaO-SiO_2-P_2O_5$ Bioactive Cement on Hardening and Hydroxyapatite Formation)

  • 박상종;김철영
    • 한국세라믹학회지
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    • 제31권5호
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    • pp.505-512
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    • 1994
  • It has been reported that a biocement obtained by mixing CaO-SiO2-P2O5 glass powder and ammonium phosphate solution has biocompatibility as well as high strength. However, the compositional dependence on its hardening and hydroxyapatite formation phenomena has not been studied. Therefore, the main objective of this work is to study the effects of P2O5, MgO in CaO-SiO2 system glass on the hardening and hydroxyapatite formation. When more than 50 mole% of CaO containing CaO-SiO2 glasses was reacted with ammonium phosphate solution, CaNH4PO4.H2O crystal was formed, but the glass with less than 50 mol% of CaO formed (NH4)2HPO4 and NH4H2PO4 crystals which are derived from ammonium phosphate solution without reacting with the glasses. As the amount of P2O5 in CaO-SiO2-P2O5 glass system was increased, the formation of CaNH4PO4.H2O crystal was enhanced. When those hardened samples were reacted with tris-buffer solution, hydroxyapatite was obtained only for the sample with CaNH4PO4.H2O. While the substitution of MgO for CaO decreased the formation of CaNH4PO4.H2O crystal. MgNH4PO4.H2O crystla was formed in high MgO containing glass, which did not react with tris-buffer solution.

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3CaO.3A12O3.CaSO4.CaSO4.2H2O - Ca(OH)24 - 3CaO.Al2O3계의 수화 특성 (Hydration Properties of 3CaO.3A12O3.CaSO4.CaSO4ㆍ2H2O - Ca(OH)24 - 3CaO.Al2O3 System)

  • 배승훈;송종택
    • 한국세라믹학회지
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    • 제40권9호
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    • pp.859-866
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    • 2003
  • 칼슘설포알루미네이트계 팽창시멘트는 수화하여 ettringite, monosulfate 등의 수화물을 생성하여 경화체의 수축을 보삼함으로써, 균열 발생을 방지한다. 본 실험에서는 칼슘설포알루미네이트계 팽창시멘트의 수화특성을 규명하기 위하여 화학성법으로 3CaO.$3A1_2$$O_3$.$CaSO_4$($C_4$$A_3$S)을 제조하였으며, $C_4$$A_3$S-Ca(OH)$_2$-CaSO$_4$.2$H_2O$-C$_3$A계의 수화특성을 알아보았다. 화학성법에 의해 $1300^{\circ}C$에서 잘 발달한 $C_4$$A_3$S를 제조할 수 있었고, $C_4$A$_3$S-Ca(OH)$_2$-CaSO$_4$.2$H_{2}O$계의 주요수화 생성물은 ettringite이었으며, $C_4$A$_3$S-Ca(OH)$_2$-CaSO$_4$.$2H_2O$-C$_3$A는 수화초기에 ettringe를 생성하였다가 석고가 소비되면서 monosulfate로 전이하였다.

Bi-Sr-Ca-O계에서 초전도상의 형성에 관한 상평형 (Phase Equilibria for the Formation of Superconducting Phases in the Bi-Sr-Ca-O System)

  • 김철진
    • 한국재료학회지
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    • 제3권4호
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    • pp.410-421
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    • 1993
  • Bi-Sr-Ca-O 초전도성계에서 $Bi_2O_3-(Sr_2CaCu_2O_x$)의 pseude binary계를 선택하여 $Sr_2CaCu_2O_x$$Bi_2O_3$를 5%단위로 40 cation mole% Bi까지 첨가하면서 $850^{\circ}C$ 초전도상 및 공존하는 상들의 평형 및 반응 경로들을 XRD, SEM, EDS, DTA를 이용하여 분석하였다. Bi의 함량이 35 mole% Bi보다 클 때에는 $Bi_2Sr_2CaCu_2O_8$상과 공존하는 액상이 형성되며 2212상의 액상으로 존재하며 액상의 냉각시 제일 먼저 $Bi_2Sr_2CaCu_2O_8$상 주의에 석출된 것이 관찰되었다.

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3CaO.$Al_2O_3$의 수화반응에 미치는 글루콘산나트륨읨 영향(I) -흡착거동- (Ettect of Sodium Gluconate on the Hydration of 3CaO.$Al_2O_3$(I)-Adsorption Behavior-)

  • 김창은;이승헌;유종석;최진호
    • 한국세라믹학회지
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    • 제23권2호
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    • pp.38-42
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    • 1986
  • The adsorption behavior of 3CaO.$Al_2O_3$-sodium gluconate-$H_2O$ system by measuring adsorp-tion isotherm DTA and IR sepctra. The adsorbed amount of sodium gluconate on 3CaO.$Al_2O_3$ is exceedingly larger than 3CaO.$SiO_2$ and portland cement. From the DAT experiment the formation of complex is observed by the characteristic exothermic peak of the complex at 45$0^{\circ}C$ It is now strong deduced that the chemical bonding between gluconate anion and 3CaO.$Al_2O_3$ should be coordinative due to the complex formation on the surface 3CaO.$Al_2O_3$ from the IR spectra of sod-ium gluconate only and 3CaO.$Al_2O_3$ -sodium gluconate-$H_2O$.

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$Al_2O_3-CaO-Cr_2O_3$ 계 내화물의 고온 안정성 (High Temperature Stability for Refractories of the System $Al_2O_3-CaO-Cr_2O_3$)

  • 이홍립
    • 한국세라믹학회지
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    • 제17권1호
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    • pp.8-12
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    • 1980
  • CaO was added to the $MgAlCrO_4$ spinel, a main component of the mag-chro refractroies, by 0, 1, 5 and 10 mol% before sintering at 135$0^{\circ}C$ in air. The X-ray diffraction analysis produced an additional X-ray diffraction pattern of 8CaO.$6Al_2O_3$.$2CrO_3$ besides that of $MgAlCrO_4$. The formation of 8CaO.$6Al_2O_3$.$2CrO_3$ was interpreted as due to the presence of CaO.8CaO.$6Al_2O_3$.$2CrO_3$ was unstable and easily vaporized. It was concluded that formation of the unstable pollutant 8CaO.$6Al_2O_3$.$2CrO_3$ could be prevented in reducing atmospheres. It was found that the basic refractories containing $Al_2 O_3 -CaO-Cr_2 O_3$ system would be more stable and much less toxic in reducing at mospheres than in oxidizing stmosphere.

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Zinc borosilicate 유리의 CaO 첨가에 따른 항균력 개선 효과 검증 (Effect of CaO on the antibacterial property of zinc borosilicate glasses)

  • 황민성;정재엽
    • 한국결정성장학회지
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    • 제33권5호
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    • pp.187-190
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    • 2023
  • 본 연구에서는 ZnO-Na2O-B2O3-SiO2 계 유리에 CaO의 첨가에 따른 유리의 열적, 화학적 특성, 표면 제타전위 및 항균특성을 분석하였다. 유리 조성에 따른 열적 특성은 DTA 분석을 통해 확인하였고, 30ZnO-xCaO-20Na2O-30B2O3-(20-x)SiO2 (x = 0, 2, 4, 6, 8, 10 mol%)계 유리에서 CaO 함량이 증가함에 따라 유리전이온도가 줄어드는 것을 확인하였다. CaO 함량이 늘어날수록 유리 구조가 약화됨에 따라 더 많은 Zn2+ 이온이 용출되었고, 알칼리 및 알칼리 토류의 초기 급속한 용출로 인해 유리의 표면 제타전위가 증가함을 확인하였다. 이러한 이유로 유리의 항균활성 또한 급격하게 개선됨을 확인하였으며, 대장균(gram negative)과 황색포도상구균(gram positive) 모두에 대해 99.9 % 항균 활성을 갖는 항균 유리를 개발할 수 있었다.

새로운 파이로클로어의 합성 및 결정화학적 특징 (Synthesis and Crystal Chemistry of New Actinide Pyrochlores)

  • 장영남;채수천;배인국
    • 한국광물학회지
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    • 제15권1호
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    • pp.78-84
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    • 2002
  • New pyrochlore-type phases($A_2$$B_2$$O_{7}$) were synthesized in the systems: CaO-C$eO_2$-T$iO_2$, CaO-$UO_2$(T$hO_2$)-Z$rO_2$, CaO-$UO_2$(T$hO_2$)-$Gd_2$$O_3$-T$iO_2$-Z$rO_2$, 및 CaO-T$hO_2$-S$nO_2$. The starting materials were pressed with the pressure of 200~400 MPa and sintered at 1500~ 155$0^{\circ}C$ for 4~8 hours in air and at 1300~ 135$0^{\circ}C$ for 5 ~50 hours under oxygen atmosphere. The products were characterized using XRD, SEM/EDS and TEM. In the bulk compositions of CaCe$Ti_2$$O_{7}$, CaTh$Zr_2$$O_{7}$,($Ca_{0.5}$ Gd$Th_{0.5}$)(ZrTi)$O_{7}$) ($Ca_{0.5}$Gd$Th_{0.5}$)(ZrTi)$O_{7}$, ($Ca_{0.5}$G$dU_{0.5}$)(ZrTi)$O_{7}$ and CaTh$Sn_2$$O_{7}$ , pyrochlore was the major phase, together with other oxide phase $of_2$$O_{7}$ fluorite structure. In the samples with target compositions CaU$Zr_2$$O_2$$Ca_{0.5}$ G$dU_{0.5}$)$Zr_2$T$iO_{7}$ pyrochlore was not identified, but a fluorite-structured phase was detected. The formation factor as the stable phase depended on crystal chemical characteristics of the actinide and lanthanide elements of the system concerned.

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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