<p>As a core load-bearing component of railway systems, heavy rail steel is prone to crack initiation induced by inclusions during service, which adversely affects its fatigue life. Owing to its excellent deoxidation, desulfurization, and inclusion modification capabilities, the rare earth element Ce is considered an effective approach to improving steel quality. A combined approach of thermodynamic calculations, high-temperature melting experiments, and crystallographic analysis was employed to systematically investigate the modification mechanism of inclusions and the heterogeneous nucleation behavior induced by Ce in heavy rail steel. The results show that the primary inclusions in untreated heavy rail steel are large, irregular MnS particles and nearly spherical Al<sub>2</sub>O<sub>3</sub>–SiO<sub>2</sub>–CaO complex inclusions. After Ce addition, Ce reacts not only with free O, S, and Al in the molten steel but also modifies the existing inclusions into smaller, more spherical or ellipsoidal CeAlO<sub>3</sub>, Ce<sub>2</sub>O<sub>3</sub>, Ce<sub>2</sub>O<sub>2</sub>S, and their composite forms. Due to the better toughness of Ce<sub>2</sub>O<sub>3</sub> and Ce<sub>2</sub>O<sub>2</sub>S, when they envelop the harder CeAlO<sub>3</sub> core, they help alleviate stress concentration at the interface with the steel matrix, thereby improving the mechanical properties of the steel. With the&#xa0;increasing Ce content, the inclusion size shows a trend of first decreasing and then increasing. The optimal modification effect is observed when the Ce content is in the range of 0.0017%–0.0026%. The overall evolution sequence of inclusions is as follows: Al<sub>2</sub>O<sub>3</sub> + MnS→ CeAlO<sub>3</sub> + MnS→ Ce<sub>2</sub>O<sub>2</sub>S + MnS→ Ce<sub>2</sub>O<sub>2</sub>S + Ce<sub>2</sub>S<sub>3</sub>→ Ce<sub>2</sub>O<sub>2</sub>S + Ce<sub>3</sub>S<sub>4</sub> + CeS→ Ce<sub>2</sub>O<sub>2</sub>S + CeS. Furthermore, the two-dimensional lattice disregistry analysis reveals that rare earth inclusions exhibit better lattice matching with γ-Fe than Al<sub>2</sub>O<sub>3</sub>, indicating stronger heterogeneous nucleation potential. During solidification, Ce<sub>2</sub>O<sub>3</sub> and Ce<sub>2</sub>O<sub>2</sub>S tend to nucleate on CeAlO<sub>3</sub> surfaces to form complex inclusions, which in turn provide nucleation sites for γ-Fe and promote grain refinement.</p>

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Modification of inclusion and heterogeneous nucleation behavior in heavy rail steel treated with rare earth

  • Qian Meng,
  • Yi Wang,
  • Wen Wang,
  • Jian-Zhong He,
  • Jian-Xun Fu

摘要

As a core load-bearing component of railway systems, heavy rail steel is prone to crack initiation induced by inclusions during service, which adversely affects its fatigue life. Owing to its excellent deoxidation, desulfurization, and inclusion modification capabilities, the rare earth element Ce is considered an effective approach to improving steel quality. A combined approach of thermodynamic calculations, high-temperature melting experiments, and crystallographic analysis was employed to systematically investigate the modification mechanism of inclusions and the heterogeneous nucleation behavior induced by Ce in heavy rail steel. The results show that the primary inclusions in untreated heavy rail steel are large, irregular MnS particles and nearly spherical Al2O3–SiO2–CaO complex inclusions. After Ce addition, Ce reacts not only with free O, S, and Al in the molten steel but also modifies the existing inclusions into smaller, more spherical or ellipsoidal CeAlO3, Ce2O3, Ce2O2S, and their composite forms. Due to the better toughness of Ce2O3 and Ce2O2S, when they envelop the harder CeAlO3 core, they help alleviate stress concentration at the interface with the steel matrix, thereby improving the mechanical properties of the steel. With the increasing Ce content, the inclusion size shows a trend of first decreasing and then increasing. The optimal modification effect is observed when the Ce content is in the range of 0.0017%–0.0026%. The overall evolution sequence of inclusions is as follows: Al2O3 + MnS→ CeAlO3 + MnS→ Ce2O2S + MnS→ Ce2O2S + Ce2S3→ Ce2O2S + Ce3S4 + CeS→ Ce2O2S + CeS. Furthermore, the two-dimensional lattice disregistry analysis reveals that rare earth inclusions exhibit better lattice matching with γ-Fe than Al2O3, indicating stronger heterogeneous nucleation potential. During solidification, Ce2O3 and Ce2O2S tend to nucleate on CeAlO3 surfaces to form complex inclusions, which in turn provide nucleation sites for γ-Fe and promote grain refinement.