The purpose of the study was to determine how the casting temperature and the time the molten metal is kept in the furnace affect the chemical composition and carbon equivalent of gray cast iron.
The input material of gray cast iron with a known chemical composition was remelted in an electric induction melting furnace. After melting, the melt was heated to temperatures of 1300, 1350, and 1400 °C. At each temperature, the melt was held for 0, 15, 30, and 45 minutes. At these temperatures and holding times, samples were taken for chemical analysis, where the melt was cast into a copper mold. Samples for thermal analysis were also cast using the ATAS system, whereby the melt was poured into a Quick cup measuring cell. The temperature was measured during the cooling of the melt. A thermodynamic analysis was performed based on the chemical compositions. Using Thermo-Calc and JMatPro software, we calculated the change in Gibbs free energy of oxidation reactions at given temperatures from the chemical composition of the input material, as well as the carbon equivalent. The oxidation reaction calculations were normalized to 1 mol of oxygen. The aim was to determine the degree of oxidation of carbon and other alloying elements in gray cast iron, how the chemical composition and carbon equivalent change.
The results showed that the casting temperature and the time the melt is held in the furnace have a significant influence on the degree of oxidation and the final chemical composition. At higher casting temperatures, the oxidation of carbon and other alloying elements is more intense than at lower casting temperatures. With longer holding times of the melt in the furnace, more carbon and other alloying elements were oxidized. Observations have shown that at lower casting temperatures, silicon and manganese burn off more, while at higher casting temperatures, carbon burns off more. The carbon equivalent and active carbon equivalent decrease as the casting temperature increases. It has been found that carbon has the greatest influence on the carbon equivalent.
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