• Journal of the Korean Ceramic Society
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• v.35 no.12
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• pp.1301-1307
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• 1998

For dolomite clinkers used as stamp materials the corrosion behavior of those by molten steel was investigated in therange of temperatures between 1550$^{\circ}C$ and 1600$^{\circ}C$ IN hot face the dicalciumferrite of magnesioferrite and dicalciumferrite formed within dolomite clinkers was preferentially dissolved into molten steel and the protective layer of magnesioferrite was formed. For dolomite clinker without Fe2O3 magnesioferrite maintained the skeleton of MgO while the skeleton of CaO disappered bythe formation of dicalciumferrite and it existed as grain boundary phases of magnesioferrite. For dolomite clinker with Fe2O3 was diffused into hot face by the decomposition of dicalciumferrite. With increasing temperature of molten steel the formation depth of dicalciumferrite was increased and the magnesioferrite layer in hot face was decreased for dolomite clinker without Fe2O3 while the layer thickness and grain sizes of magnesioferrite in hot face was decreased for dolomite clinker without Fe2O3 while the layer thickness an grain sizes of magnesioferrite in hot face was increased due to the increment of the decomposition reaction of dicalciumferrite for dolomite clinker with Fe2O3.

• Journal of the Korean Ceramic Society
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• v.36 no.1
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• pp.30-35
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• 1999

For dolomite clinkers used as stamp materials, the corrostion behavior of those by slag was inverstigated between 1550$^{\circ}C$ and 1650$^{\circ}C$. Fe2O3 among slag components was selectively penetrated into the grain boundaries of dolomite clinkers. In hot face, the magnesioferrite was preferentially formed by Fe2O3 component contained in dolomite clinker rather than Fe2O3 of slag. The corrosion steps of dolomite clinkers by slag were found as follows ; (1) The dicalciumferrite was formed by the reaction of the calcia within dolomite clinkers with Fe2O3 of slag. (2) The magnesia within dolomite clinkers reacted with the dicalciumferrite to from magnesioferrite and the residual calcia within dolomite clinkers reacted with the dicalciumferrite to form magnesioferrite and the residual calcia was dissolved into slag. (3) The magnesioferrite was corroded by CaO-SiO2 compounds of slag. With the temperature of slag increased, the magnesioferrite layer in hot face was decreased for dolomite clinker without Fe2O3 while the layer thickness and grain sizes of magnesioferrite was increased for dolomite clinker with Fe2O3.

• Journal of the Korean Ceramic Society
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• v.34 no.7
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• pp.738-746
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• 1997

MgO clinker and two kinds of dolomite clinkers with different microstructures and CaO contents were used as starting materials, and the effects of Fe2O3 addition on the properties of MgO and dolomite were investigated in the range of 2 to 8 wt% of Fe2O3 content. Secondary phases contributed to densification of MgO-Fe2O3 and dolomite-Fe2O3 were magnesioferrite and dicalciumferrite, respectively. Sinterabilities of MgO-Fe2O3 and dolomite-Fe2O3 were directly proportional to the amount of secondary phases. Also, sinterability of dolomite itself was dependent on the microstructure of starting material including distribution of CaO and MgO as well as the addition amount of Fe2O3. The flexural strength of MgO-Fe2O3 content was almost constant. The hydration resistance of dolomite with large size of MgO and discontinuous distribution of CaO was higher than that of dolomite with small size of MgO and continuous distribution of CaO. Also, the minimum content of Fe2O3 to prevent they hydration of dolomite was about 4wt%. As increasing Fe2O3 content, the penetration resistance of MgO-Fe2O3 was improved by the increment of magnesioferrite. On the other hand, the penetration resistance of dolomite-Fe2O3 was decreased because of the increment of dicalciumferrite having low melting point.