Papers by Keyword: Fe₃C

Abstract: The recrystallization behaviors of 60% rolled Fe-wt.3%Si and Fe- wt.3%Si-Mn-S alloys containing coarsen MnS particles were observed in temperature range 600°C~1000°C. The activation energy for recrystallization was determined according to an Arrhenius type of relationship. It was found that the activation energy in the temperature range 600°C~750°C was much higher than that in the temperature range 850°C~1000°C. Thermo-mechanical calculation indicates that there are hardly precipitation behaviors of MnS particles in 600°C~1000°C. Fe₃C will precipitate below 650°C and Cottrell atmosphere will form just above 650°C, which induces dragging effect against the boundary migration during recrystallization and increase the activation energy. The activation energy determined was about 99kJ/mol or 217kJ/mol in Fe-3%Si alloy and 91kJ/mol or 220kJ/mol in Fe-3%Si-Mn-S alloy for the recrystallization in high temperature range of 850°C~1000°C or low temperature range of 600°C~750°C respectively.

Abstract: Thermodynamic data for the substitution of silicon and manganese in cementite have been estimated using first-principles methods in order to aid the design of steels where it is necessary to control the precipitation of this phase. The need for the calculations arises from the fact that for silicon the data cannot be measured experimentally; manganese is included in the analysis to allow a comparison with its known behaviour. The calculations for Fe3C, (Fe11Si4c)C4, (Fe11Si8d)C4, (Fe11Mn4c)C4 and (Fe11Mn8d)C4 are based on the total energy all-electron full-potential linearized augmented plane-wave method within the generalized gradient approximation to density functional theory. The output includes the ground state lattice constants, atomic positions and bulk moduli. It is found that (Fe11Si4c)C4 and (Fe11Si8d)C4 have about 52 and 37 kJ greater formation energy when compared with a mole of unit cells of pure cementite, whereas the corresponding energy for (Fe11Mn4c)C4 and (Fe11Mn8d)C4 is less by about 5 kJ mol1. These results for manganese match closely with published trends and data; a similar comparison is not possible for silicon but we correctly predict that the solubility in cementite should be minimal.