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Katsuhiko Inoue, T. Ikeda (1982)
The Solid Solution State and the Crystal Structure of Calcium Ferrite Formed in Lime-fluxed Iron OresTetsu To Hagane-journal of The Iron and Steel Institute of Japan, 68
B. Phillips, A. Muan (1959)
Phase Equilibria in the System CaO‐Iron Oxide‐SiO2, in AirJournal of the American Ceramic Society, 42
M. Pownceby, Tim Patrick (2000)
Stability of SFC (silico-ferrite of calcium) solid solution limits, thermal stability and selected phase relationships within the Fe2O3-CaO-SiO2 (FCS) systemEuropean Journal of Mineralogy, 12
E. Costa, J. Coheur, B. Vanderheyden, R. Munnix (1995)
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Quenching experiments were used to investigate the solid solution range, thermal stability, and selected phase relationships of silico-ferrite of calcium and aluminum (SFCA) within the Fe2O3-CaO-Al2O3-SiO2 (FCAS) system. SFCA was found to be stable within a plane that connects the end members CF3 (CaO·3Fe2O3), CA3 (CaO·3Al2O3), and C4S3 (4CaO·3SiO2). Chemical substitution in the four component system follows the coupled substitution mechanism 2(Fe3+, Al3+)↔(Ca2+, Fe2+)+Si4+ with the greatest range in chemical substitution occurring in the direction of the Al3+↔Fe3+ exchange (ranging from 0 wt pct Al2O3 to ∼31.5 wt pct Al2O3). The extent of Al3+↔Fe3+ substitution decreases with increasing temperature, and it was estimated that SFCA completely decomposes by ∼1480 °C. Coupled substitution involving Ca2+ and Si4+ for 2M3+ is not as extensive as the Al3+↔Fe3+ exchange, having a maximum range between 3 and 11 wt pct C4S3 component. Additional phases encountered in the experimental program included hematite; magnetite; quench liquid; dicalcium silicate; Fe-bearing gehlenite; calcium alumino-ferrite solid solutions, C(A, F)6 and C(A, F)2, plus an unidentified phase, possibly representing a solid substitution between SFCA-I and C(A, F)3. Schematic phase diagrams have been constructed to show the relationship of SFCA with these surrounding phases.
Metallurgical and Materials Transactions B – Springer Journals
Published: Apr 13, 2002
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