Abstract

Martensitic and nanobainite transformations are studied in situ in a low alloyed, high-Si steel by using in situ HEXRD, combined with dilatometry and SEM observations, and by considering the same steel composition and austenitization conditions. The martensitic microstructure presents a mixed lath-plate morphology with large scatter of sizes whereas the bainite microstructure shows finer laths with more uniform sizes. Recently introduced methods are used to track in situ by HEXRD, in one single experiment, the phase fractions, the distribution of the carbon and the evolution of the dislocation densities. The study of nanobainite revealed that about two thirds of the carbon partitions from the ferrite to precipitate into transition iron carbides or to enrich the austenite. Both processes occur very fast after the formation of each nanobainite lath, but the ferrite remains largely supersaturated in carbon. The dislocation density increases inside each new forming bainitic ferrite lath. It then decreases when recovery becomes preponderant, as described with a recovery model from the literature. After the martensitic transformation, the retained austenite ends up with high hydrostatic compressive stresses. Dislocation densities are higher than in nanobainite and probably more heterogeneous, because recovery is less significant. No carbides were detected, contrary to the nanobainite. The carbon mass balance is analyzed in the light of these new results and previous investigations on similar systems. • Same steel composition and austenitization treatment to study the transformations. • Transition-carbides precipitation kinetic was quantitatively investigated. • Dislocation recovery observed during the nano-bainitic transformation. • Carbon distribution and mass balance showed a deficit of ca. 0.1 wt%.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.