Abstract

Additions of 3 and 5 wt.% Al have been investigated as a low-cost method for transformation acceleration in nano-bainitic steels. For both Al contents, two groups of steels with C-content in the range ~0.7 to ~0.95 wt.% were studied. Thermodynamic and physical simulations were used in alloy and heat treatment design. Characterization was performed via dilatometry, scanning and transmission electron microscopy, Synchrotron X-ray diffraction, and tensile and impact testing. Fast bainitic-transformation time-intervals ranging from 750–4600 s were recorded and tensile strengths up to 2000 MPa at a ductility of ~10 elongation percent were attainable for the 3 wt.% Al group at an austempering temperature of 265 °C. Higher Al additions were found to perform better than their lower Al counterparts as the austempering temperature is dropped. However, Al lowered the austenite stability, increased the martensite start temperature, austenitization temperatures and, consequently, the prior austenite grain size, as well as limiting the austempering temperatures to higher ones. Additionally, the lowered austenite stability coupled with higher additions of hardenability elements (here carbon) to maintain the martensite start at around 300 °C, causing the 5 wt.% Al group to have a large amount of low stability retained austenite (and consequently brittle martensite) in their microstructure, leading to a low elongation of around 5%.

Highlights

  • In order to optimize the properties of nano-bainite steel, it is essential to understand the nature of its transformation and consider the different factors contributing to and resulting from it

  • Thermodynamic simulation using ThermoCalc software indicates that the full austenitization temperatures are 884, 850, and 820 ◦ C for the 31, 32, and 33 alloys, respectively

  • Thermodynamic simulation using ThermoCalc software indicates that the full austenitization temperatures are 884, 850, and 820 °C for the 31, 32, and 33 alloys, respectively

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Summary

Introduction

In order to optimize the properties of nano-bainite (nB) steel, it is essential to understand the nature of its transformation and consider the different factors contributing to and resulting from it. The nucleation of bainite starts at the γ grain boundaries as well as at crystal defect sites. It further proceeds via an autocatalytic mechanism utilizing the newly generated α-γ interfaces as new nucleation sites [1,2,3,4,5]. The growth mechanism of bainite is a displacive one that is plastically accommodated by deformation in the surrounding austenite. Depending on the transformation temperature and alloying elements present, this entrapped C will either diffuse into the surrounding austenite grains, or precipitate into carbide [6]. When carbide-free, low temperature nB is desired, cementite suppressing elements (such as Si and Al) are added and, austenite is enriched with C [8]

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