4.7 Article

Microstructure and tempering softening mechanism of modified H13 steel with the addition of Tungsten, Molybdenum, and lowering of Chromium

Journal

MATERIALS & DESIGN
Volume 224, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.matdes.2022.111317

Keywords

H13 steel; Alloy elements ratio optimizing; Microstructure; Tempering softening resistance; Recrystallization mechanism

Funding

  1. Natural Science Foundation of Jiangsu Province [BK20220548]
  2. Science and Technology Department of Jiangsu Province [BE2017127]
  3. Opening Project of Jiangsu Key Laboratory of Advanced Structural Materials and Application Technology [ASMA202002]
  4. State Key Lab of Advanced Metals and Materials in University of Science and Technology Beijing [2022-Z21]

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In this study, a modified H13 steel (CXN03 steel) with additional tungsten, molybdenum, and lowering chromium was prepared to improve the tempering softening resistance (TSR) of hot work die steels. The results showed that CXN03 steel exhibited significantly better TSR compared to H13 steel, mainly due to the excellent stability of dispersive nano-sized M2C. Recrystallization softening was observed in H13 steel but not in CXN03 steel.
The rapid development in the advanced manufacturing industry asks for better tempering softening resistance (TSR) of Hot work die steels. In this work, a modified H13 steel (CXN03 steel) with additional tungsten, molybdenum, and lowering chromium was prepared. The TSR of CXN03 is significantly better than H13. After quenching at 1040 degrees C, the hardness and strength of H13 were larger than those of CXN03. However, the hardness and strength of CXN03 exceeded those of H13 after 2 h tempering at 600 degrees C. A mathematical model was utilized to correlate microstructural characteristics with yield strength during tempering. The calculated results indicated that the superior tempering softening resistance of CXN03 steel mainly results from the excellent stability of dispersive nano-sized M2C, which could prevent dislocation recovery. Recrystallization softening was observed in H13 but not in CXN03. The recrystallization of H13 is driven by dislocation movement, and the rearrangement of dislocations contributed to the formation of sub-boundaries. These sub-boundaries could divide martensite lath as well as form sub-grains. As the tempering time increased, sub-boundaries transformed into high-angle grain boundaries by absorbing the vicinal dislocations. Therefore, martensite lath collapsed, and massive recrystallized grains occurred. The massive stable M2C in CXN03 hindered the dislocation rearrangement, thus preventing the recrystallization.

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