• 한국표면공학회지
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• 제46권2호
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• pp.80-86
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• 2013

Magnesium alloys of AZ31 containing (0.5, 1, 1.5) wt.% of initially added CaO particles were cast in air, and their oxidation behavior was studied at $450-650^{\circ}C$ in air. The initially added CaO particles either decomposed to dissolve in the ${\alpha}$-Mg matrix or precipitated as $Al_2Ca$ along the grain boundaries of the matrix during casting. The ignition temperatures were $565.4^{\circ}C$ for AZ31, $608.6^{\circ}C$ for AZ31+0.5 wt.%CaO, and $689.7^{\circ}C$ for AZ31+1 wt.%CaO. No ignition occurred for AZ31+1.5 wt.%CaO up to $700^{\circ}C$, displaying good oxidation resistance. The CaO-rich oxide scales that formed on the surface of the AZ31+(0.5, 1, 1.5) wt.%CaO alloys improved the oxidation resistance of AZ31 alloys.

• 한국분말야금학회:학술대회논문집
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• 한국분말야금학회 2000년도 춘계학술강연 및 발표대회 강연 및 발표논문 초록집
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• pp.15-15
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• 2000

• 한국재료학회:학술대회논문집
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• 한국재료학회 1997년도 한국재료학회 춘계학술발표회
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• pp.77-77
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• 1997

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2015년도 춘계학술대회 논문집
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• pp.98-99
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• 2015

Mg합금은 지극히 열악한 내산화성을 갖는 MgO로 산화되기 때문에, 모든 Mg합금은 고온에서는 쉽게 산화되고 발화된다. 그러나, CaO를 첨가하면 CaO가 시편의 노출면적을 줄이고, 산소의 내부확산을 억제함으로써 시편 표면에 얇고 균일한 보호피막을 형성하여 Mg합금의 산화 저항성을 증가시켰다.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2012년도 춘계학술발표회 논문집
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• pp.172-172
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• 2012

Mg합금은 지극히 열악한 내산화성을 갖는 MgO로 산화되기 때문에, 모든 Mg합금은 고온에서는 쉽게 산화되고 발화된다. 그러나, CaO를 첨가하면 CaO가 시편의 노출면적을 줄이고, 산소의 내부확산을 억제함으로써 시편 표면에 얇고 균일한 보호피막을 형성하여 Mg합금의 산화 저항성을 증가시켰다.

• 한국주조공학회지
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• 제31권6호
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• pp.347-353
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• 2011

There is thixo-extrusion to form high strength aluminum alloy. But, it is a problem that grains become grain coarsening during reheating process because the alloy was exposed at high temperature. In order to solve grain growth during reheating process, calcium was added in Al-Zn-Mg alloys. Primary a grain sizes of semi-solid Al-Zn-Mg-(0, 0.4, 0.6 and 0.9, wt.%)Ca were measured with image analyzer after reheating. Measured primary a grain sizes were applied to LSW(Lifshitz-Slyozov and Wagner) equation to check the effect of Ca on grain coarsening. Coarsening rate constant K values of semi-solid Al-Zn-Mg-(0, 0.4, 0.6 and 0.9, wt.%)Ca alloys were $371\;mm^3s^{-1}$, $247\;mm^3s^{-1}$, $198\;mm^3s^{-1}$ and $166 mm^3s^{-1}$, respectively. As increasing calcium content, K value decreased which means grains are refined. Also, grains of calcium addition were more spherical than that of calcium free.

• 한국표면공학회지
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• 제45권4호
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• pp.155-161
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• 2012

Magnesium alloys of AZ31, AZ31 + (0.5, 1, 1.5)wt.% CaO were cast, hot rolled, and oxidized between 450 and $650^{\circ}C$ in atmospheric air. The added CaO enabled to cast the AZ31 alloy in air. It decomposed and precipitated along the grain boundaries of the AZ31 alloy as $Al_2Ca$. The more the amount of CaO was, the more $Al_2Ca$ formed. The oxidation limit was about $450^{\circ}C$ for the AZ31 alloy. But, It increased to $650^{\circ}C$ in the CaO-added alloys. Hot rolling destroyed the precipitates that formed along the grain boundaries of the AZ31 alloy. During oxidation, MgO oxide scales that incorporated CaO formed at the outer surface of the formed oxide layer.

• 한국표면공학회:학술대회논문집
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• 한국표면공학회 2015년도 춘계학술대회 논문집
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• pp.126-127
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• 2015

주방 상태의 Mg, Mg+5wt%.Ca, Mg+5wt%.Ca+1wt%.Zn 합금의 발화 실험 및 TGA를 통해 $450{\sim}600^{\circ}C$에서 고온산화실험을 실시하였다. Ca의 첨가로 내발화성 및 고온산화특성이 향상되었으며, Zn의 첨가는 내발화성과 고온산화특성 모두에 악영향을 미쳤다. 산화시킨 시편의 SEM/EDS, XRD, 및 TEM 분석을 통하여 고온산화 특성을 조사하였다.

• 한국재료학회지
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• 제7권11호
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• pp.1012-1017
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• 1997

Mg-Zn-Ca합금의 잉곳트는 BN을 내벽에 바른 4x$10^{-5}$Torr의 진공의 석영관내에서 제조하였다. Mg-Zn합금계의 입자미세화를 위하여 0.5-5wt.%조성범위의 Ca를 첨가하였다. 제조된 합금을 용체화처리한 후 결정립크기와 경도를 측정하였다. Mg-6wt.%Zn합금의 입자미세화효과는 Ca가 1.5wt%첨가 될 때 최적의 조건이었다. Mg-6wt.% Zn과 Mg-6wt.% Zn-2wt.% Ca및 Mg-6wt.% Zn-1.5wt.% Si합금을 시효처리하여 시효거동을 조사하였다. 입자미세화에 의한 경도증가효과는 Mg-Zn-Ca합금계에서 크게 나타났으며 시효에 의한 경도증가효과는 Mg-Zn-Si합금계에서 크게 나타났다. Mg-6wt.%Zn합금의 부식전류밀도는 0.5wt.% Ca의 조성에서 감소되었다.

• Corrosion Science and Technology
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• 제15권3호
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• pp.120-124
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• 2016

The effect of alloying element Ca (0, 1, and 2 wt%) on corrosion resistance and bioactivity of the as-received and anodized surface of rolled plate AM60 alloys was investigated. A plasma electrolytic oxidation (PEO) was carried out to form anodic oxide film in $0.5mol\;dm^{-3}\;Na_3PO_4$ solution. The corrosion behavior was studied by polarization measurements while the in vitro bioactivity was tested by soaking the specimens in Simulated Body Fluid (1.5xSBF). Optical micrograph and elemental analysis of the substrate surfaces indicated that the number of intermetallic particles increased with Ca content in the alloys owing to the formation of a new phase $Al_2Ca$. The corrosion resistance of AM60 specimens improved only slightly by alloying with 2 wt% Ca which was attributed to the reticular distribution of $Al_2Ca$ phase existed in the alloy that might became barrier for corrosion propagation across grain boundaries. Corrosion resistance of the three alloys was significantly improved by coating the substrates with anodic oxide film formed by PEO. The film mainly composed of magnesium phosphate with thickness in the range $30-40{\mu}m$. The heat resistant phase of $Al_2Ca$ was believed to retard the plasma discharge during anodization and, hence, decreased the film thickness of Ca-containing alloys. The highest apatite forming ability in 1.5xSBF was observed for AM60-1Ca specimens (both substrate and anodized) that exhibited more degradation than the other two alloys as indicated by surface observation. The increase of surface roughness and the degree of supersaturation of 1.5xSBF due to dissolution of Mg ions from the substrate surface or the release of film compounds from the anodized surface are important factors to enhance deposition of Ca-P compound on the specimen surfaces.