Increasing train speeds and the reduction of maintenance slots places high demands on the railway rails. To meet the challenging demands, producers regularly introduce new steel types. In this experimental investigation is the mechanical behavior of an air-cooled vanadium-alloyed hypereutectoid rail steel presented. The rail is produced applying conventional hot rolling of a reheated bloom and is then cooled on a cooling bed. The mechanical behavior is determined by performing standardized linear elastic fracture mechanics tests. The necessary specimens are extracted from new rails that are made in series production. Monotonic tensile test results have shown that the strain-hardenability of the steel is comparable to standard grade eutectoid rail steel and is higher than that of an accelerated-cooled eutectoid rail grade. The fracture toughness test results showed, statistically, no difference when compared with the fracture toughness values of the accelerated-cooled eutectoid rail grade. The tests were performed at room temperature. The fatigue crack growth rates are, in the linear Paris-regime, slightly higher than in the previously mentioned steels. The results are explained considering the distinct microstructural characteristics of the air-cooled vanadium-alloyed hypereutectoid steel and the fractured surface of the specimens. This experimental investigation contributes to selecting railway steels and predicting the actual in-service behavior.

This work discusses the microstructure evolution observed in a quenching and partitioning (Q&P)-processed martensite/austenite stainless steel during the partitioning step at 400 °C for 300 s, where distinct microstructural bands rich in austenite due to elemental segregation, evolve into a uniform distribution of austenite grains. This phenomenon is characterised and investigated using a model for the carbon partitioning from martensite to austenite coupled with the movement of the martensite-austenite interface. The observed elimination of microstructural bands is found to be related to the topological distribution of austenite grains and the heterogeneity of the thermodynamic equilibrium regime at the various interfaces governing the partitioning process. Furthermore, the concurrence of banding elimination (local equilibrium) and phase growth towards the global equilibrium phase fractions is investigated in the simulations in terms of the role of Mn. It is found that the local equilibrium-negligible partitioning (LENP) conditions lead to the most realistic outcome.

This work presents an investigation of the microstructure development during the application of the quenching and partitioning (Q&P) process to two stainless steels with different Mn content. The results are compared with calculations based on the constrained carbon equilibrium theory, paying special attention to the presence of reactions competing for the carbon available for partitioning and to the effect of alloying element segregation. Results show that chromium carbides must be considered when accounting for the carbon available for austenite stabilisation. Moreover, manganese/chromium segregation bands play an important role in the microstructure development, particularly in martensite formation, with important consequences in the microstructure development during the following processing steps.

While experiments show that refining the prior austenite grain size can either accelerate or decelerate bainite formation in steels, kinetic models based on the successive nucleation of bainitic ferrite subunits can only predict an acceleration. In this work we develop a physically-based model for bainite kinetics assuming a displacive growth mechanism which is able to reproduce both faster and slower bainite formation kinetics induced by austenite grain refinement. A theoretical analysis of the model and comparison against published experimental data show that slower kinetics for smaller grains is favored as the difference between the activation energy for grain boundary and autocatalytic nucleation of bainite increases, and as the austenite grain refinement results in finer bainite sub-units. We also theoretically analyze the density of initially present potential nucleation sites for bainite and show that the values of density used in other published bainite nucleation models are mostly underestimated. After using physically consistent values for the density of potential nucleation sites, we were able to calculate the apparent lengthening rate of bainite sheaves which were in line with experimentally measured lengthening rates.

Carbon segregation to defects in martensite is a phenomenon known for its occurrence and interference with mechanisms such as carbon partitioning in multiphase steels. Especially in martensite–austenite partitioning processes, carbon trapping at/de-trapping from martensite defects plays an important role since it interacts with the austenite enrichment. In this work, we develop a physics-based model in which we incorporate the concurrent evolution of carbon partitioning and trapping at/de-trapping from martensite defects. The model describes the global and local, time-dependent distribution of carbon between three lattice types, namely martensite defects, martensite solid solution, and austenite. We implement the model in mean-field and full-field descriptions, and discuss the interaction between carbon enrichment in austenite and segregation to martensite defects, on the basis of global equilibrium as well as on the carbon kinetics. We apply the model in several martensite — austenite microstructures and discuss the dependence of the interaction between carbon partitioning and trapping at/de-trapping from defects on specific microstructural features, i. e. phase fractions and microstructural banding.

The present article investigates the influence of chemical composition and phase fractions on the corrosion behaviour of industrially produced quenching and partitioning (Q&P) martensitic stainless steels. Localised corrosion was analysed by scanning Kelvin probe force microscopy (SKPFM) and scanning electrochemical microscopy (SECM) in 3.5 wt.% NaCl solution. SKPFM revealed a Volta-potential difference of around 40 mV between inclusions and the matrix, which is larger than the Volta potential variations within the matrix. This difference in surface potential is a driving force for selective dissolution (corrosion initiation) at inclusions and inclusion/matrix interfaces. SECM detected early pitting initiation, particularly in alloys containing MnS and TiN inclusions. Results suggest that pitting initiation and propagation occur at those specific regions. This study emphasised that irrespective of chemical composition and phase fraction, localised corrosion initiation in Q&P-processed martensitic stainless steels is predominantly governed by the presence of inclusions.

Recent studies have demonstrated the viability of quenching and partitioning (Q&P) treatment for processing martensitic stainless steels showing an improved balance of high strength and sufficient ductility. However, to date, the fatigue behaviour of these materials has not been explored. This study examines the effect of their complex hierarchic microstructure on high cycle fatigue performance. Three steels with different alloying element contents underwent Q&P processing, resulting in multiphase microstructures rich in retained austenite. High cycle fatigue tests and analysis of fatigue fracture surfaces were performed using SEM and EBSD techniques. The results indicate satisfactory high cycle fatigue performance in Q&P treated martensitic stainless steels, surpassing traditional counterparts. Fatigue cracks predominantly form and propagate along martensite packet and block boundaries, while prior austenite grain boundaries and MnS inclusions have minimal influence on fatigue crack formation and growth. Microplastic deformation at the fatigue crack tip enhances local KAM values and triggers localized transformation of retained austenite grains. It is hypothesized that the developed Q&P treated martensitic stainless steels exhibit improved resistance to low cycle fatigue.

Localised laser treatments enable the creation of sophisticated austenite/martensite mesostructures in Fe–Ni–C steel with the potential of achieving enhanced mechanical performance. The control of phase topology is essential to modify the properties of these structures on demand and requires a profound understanding of the effect of the processing parameters on the development of the different phases upon the application of laser treatment. In this work, the microstructure evolution under exceptional gradients in temperature and heating rates is thoroughly investigated. The extent of the laser-affected zone and the heat input were tailored by varying laser parameters and specimen thickness, based on a model that considers transient material properties and the coupling between temperature and microstructure. The predicted temperature fields resulted in a complex interplay between martensite to austenite phase transformation and martensite tempering. Considering the high heating rates of up to 25000 K/s and the observed microstructures, it is suggested that austenite was formed by a pseudo-displacive mechanism and subsequently fully recrystallised in the zones most directly affected by the laser heat source. A smooth strength transition from austenite to martensite, affected by the laser parameters, could be exploited for more effective deformation mechanisms and improved material mechanical properties.

Quenching and partitioning (Q&P) treatment has been proven effective in manufacturing advanced high strength steels with high content of retained austenite, showing the improved balance of high strength and sufficient ductility. This method has been very well elaborated for carbon steel processing over the last two decades. Though it can also be potentially applied for processing other steel families, this has been scarcely studied. This article focuses on the effect of chemistry and heat treatment parameters on the microstructure and properties of Q&P treated martensitic stainless steels. Three different martensitic stainless steels with different contents of alloying elements are subjected to Q&P processing with varying quenching temperature or partitioning temperature and partitioning time. The tensile behavior of the Q&P treated steels is studied. The effect of chemistry and Q&P treatment parameters on the microstructure and tensile properties is analyzed. The effect of plastic deformation on the microstructure of the Q&P treated steels is also investigated. It is demonstrated that the Q&P treated martensitic stainless steels can show a good combination of enhanced strength and sufficient tensile ductility. Their uniform elongation increases with the increasing volume fraction of retained austenite due to the transformation induced plasticity (TRIP) effect. The ability of the martensitic matrix to accumulate plastic deformation also plays an important role. The Q&P process - microstructure - property relationship is discussed.

In many commercial steel processing routes, steel microstructures are reverted to an austenitic condition prior to the final processing steps. Understanding the microstructure development during austenitization is crucial for improving the performance and reliability of the microstructure that forms from austenite. In this work, austenite formation in a high-C steel (0.85 wt%) from a microstructure containing martensite/austenite and bainite bands is investigated. It is shown that austenite formation from bainite results in a refined austenite grain structure, and the martensite matrix thus obtained on quenching has a homogeneous distribution of carbides with a relatively low fraction of retained austenite (24%). On the other hand, a coarser austenite microstructure is obtained when austenite forms from a mixture of martensite and retained austenite. The reason for the coarse austenite grains is argued to be a memory effect, which is substantiated by in situ X-ray diffraction analysis. After quenching, an inhomogeneous carbide distribution and a higher retained austenite fraction (30%) are observed in the regions that were initially martensite/austenite. The global microstructure, hence, has a bimodal size distribution of prior austenite grains and carbide-dense bands. The causes for these heterogeneities are discussed with the help of interrupted quench experiments, equilibrium phase calculations, and DICTRA simulations.

The influence of carbon concentration variations on pearlite formation (20 h at 600 °C) in a case-carburized steel is investigated. The resultant microstructure shows three distinct regions: carburized case, a transition region, and the original core. The microstructural transition from the case to the core regions is observed to be relatively sharp. The investigated region of the carburized case (0.9 wt.% C) contains two types of pearlite: ferrite + cementite and ferrite + M₂₃C₆, where the pearlitic aggregate with M₂₃C₆ shows faster formation kinetics. The kinetics of pearlite formation in the transition region (0.3 wt.% C) is very slow and is observed with only M₂₃C₆ carbide. Only around 40% austenite decomposes into pearlite in the transition region, which, in comparison to the carburized case region of 0.9 wt.% C is a fraction that is lower by a factor of two. Pearlite is absent in the investigated core region (0.16 wt.% C). The microstructure in this region is predominantly martensite and pro-eutectoid ferrite, with a fraction of ferrite well below the equilibrium fraction. Ferrite formation in this region is limited by the redistribution of mainly Ni, Mn, and Cr, and their resulting solute drag effect on the austenite/ferrite interface. A thermodynamic and kinetic argumentation of these observations is provided with the help of thermodynamic data, precipitation simulations, and a general mixed-mode Gibbs energy balance model.

This work presents constitutive equations and a dataset of a thermal model for the prediction of temperature fields and heating rates during the application of localized laser treatments to a Fe-C-Ni alloy. The model considers transient material properties and the coupling between temperature and microstructure, with emphasis on the phase dependence of the thermal parameters and the hysteresis in the phase change. The model can predict temperature fields that are in agreement with the experimental microstructures at the laser-affected zones. This model can be applied to other materials exhibiting solid-state transformations upon the application of laser treatments.

The realisation of sophisticated hierarchically patterned multiphase steels has the potential to enable unprecedented properties in engineering components. The present work explores the controlled creation of patterned multiphase steels in which the patterns are defined by two different crystal structures: face centre cubic or fcc (austenite) and body centre cubic or bcc (martensite). These austenite/martensite mesostructures are generated by solid–solid phase transformations during the application of localised laser heat treatments in a Fe-Ni-C alloy. In particular, four patterned configurations are analysed in this work consisting of one or two horizontal austenite line structures imprinted in a base of as-quenched or tempered martensite. Digital image correlation analysis during tensile testing of the developed materials showed that both the strength of the base martensite and the mesostructure at the gauge have a strong effect on the resulting properties. Clear differences were observed among the configurations in strain partitioning, hardening of the different constituents and failure. The uniform elongation and tensile strength are increased with respect to that of the reference martensite and austenite, respectively. Concepts explored in this work can be extended to more complex patterns and other base microstructures, opening novel strategies to engineer properties in steel and other alloys.

Bainite to austenite reversal is one of the grain refinement techniques employed in carburized steels. However, chemical segregation influences the homogeneity of the bainitic structure, which is seminal to exploit the advantages associated with austenite reversal. It is therefore important to understand the influence of chemical segregation on bainite formation, which is investigated in this work. Characterizations were performed on the microstructures obtained from the case and core regions of a carburized steel after 30 h of bainite treatment at 320 °C for two carbon compositions: 0.85 wt% C (z_case) and 0.16 wt% C (z_core). The microstructure of z_case is shown to contain bands with bainite in alloy-lean regions and martensite/austenite in alloy-rich regions. For z_core, although the chemical bands are not composed of different phases, the alloy-rich regions have a fraction of martensite-austenite (MA) islands that is twice the fraction in alloy-lean regions. Despite this difference, the austenite phase fractions in the chemical bands of z_core are low and almost similar, indicating that the MA islands are mostly martensite. From experimental results and thermodynamic and kinetic simulations, it is elucidated that a different rate of phase transformation in the chemical bands is the cause for the observed microstructural inhomogeneities.

Nucleation is the re-arrangement of a small number of atoms in the structure of a material leading to a new phase. According to the classical nucleation theory, a nucleus will grow if there is an energetically favourable balance between the stability of the newly formed structure and the energy costs associated to the formation of strains and new phase boundary. However, due to their atomic and dynamic nature, nucleation processes are difficult to observe and analyse experimentally. In this work, atomic mechanisms and thermodynamics of the homogeneous nucleation of BCC phase in FCC iron have been analysed by molecular dynamics simulations. The study shows that atomic system circumvents the high energy barrier for homogeneous nucleation that would occur according to the classical nucleation theory by opting for alternative, nonclassical nucleation processes, namely coalescence of subcritical clusters and stepwise nucleation. These observations show the potential of nonclassical nucleation mechanisms in metals.

The volume increase and shape change during austenite to martensite transformation in dual-phase (DP) steels are largely accommodated in the microstructure by the deformation of the surrounding ferrite matrix. Accurate estimation of transformation-induced deformation of ferrite via experiments and modeling is essential for predicting the subsequent mechanical behavior of DP steels. This study aims to illustrate the disadvantages of simplifying the anisotropic transformation deformation of martensite to isotropic dilatation for modeling the transformation-induced deformation of ferrite. A novel methodology is developed comprising sequential experimental and numerical research on DP steels to quantify transformation-induced strains in ferrite. This methodology combines the results of prior austenite grain reconstruction, phenomenological theory of martensite crystallography and electron backscatter diffraction (EBSD) orientation data to estimate variant-specific transformation deformation. Subsequently, by comparison of full-field micromechanical calculation results on a virtual DP steel microstructure with experimental EBSD kernel average misorientation and geometrically necessary dislocation measurement results it is shown that neglecting the shear deformation associated with the martensitic transformation leads to significant underestimation in the prediction of transformation-induced strains in ferrite.

The martensitic transformation in pure Fe and its alloys has been studied over many decades. Several theoretical models have been proposed to describe the atomic motion that leads to the fcc-to-bcc martensitic transformation. However, such models do not account for the effect of pre-existing planar defects such as twin boundaries and stacking faults, present in the high-temperature austenite phase prior to the transformation process. This work systematically studies the role of nano-spaced planar faults with different inter-spacing on the martensitic transformation using molecular dynamics simulations. Research shows that the investigated planar defects affect the nucleation and growth mechanisms during martensite formation, the morphology of the resulting microstructure, the specific atomic path leading to the phase transformation, and the martensite start temperatures. Martensite variants were identified by the analysis of the atomic shears and slip systems during the transformation process. A crystallographic analysis is done to explain the existence of different shear mechanisms of martensite transformation at different locations in the fcc austenite. The present investigation provides fundamental insights into the martensitic transformation process in presence of pre-existing planar defects and can be applied to other material systems, e.g., Fe alloys.

Quenching & Partitioning (Q&P) steels owe their good strength-ductility combinations to the martensite/austenite (α’/γ) mechanical interactions and to the formation of mechanically-induced martensite (α′_mech) through the transformation-induced plasticity (TRIP) effect. An essential role is played by carbon, whose distribution among the phases can be modified through the Q&P route. This study presents a methodology to systematically and quantitatively examine the influence of the α’/γ mechanical interactions on the overall work hardening of the steel with respect to the role of carbon in the martensite. The methodology rests on the generation of a 3D micro-mechanical model that allows to derive, by crystal plasticity simulations, the overall response of a mechanically-stable α’/γ virtual microstructure. In combination with theoretical knowledge on hardening, the comparison between the experimental and simulated mechanical responses enables the quantification of the influence of the martensite carbon content and distribution on the overall TRIP strengthening contribution of the steel. The approach is applied to two low carbon Q&P-processed α’/γ microstructures of similar initial volume fractions of austenite and α′_mech formation kinetics with strain, but one containing a Nb-microaddition and displaying improved strength-ductility values. It is shown that the martensite strength and work hardening ability might additionally enhance or partially counteract the strengthening contribution from the austenite-to-α′_mech transformation during uniaxial loading. The results of this study highlight that the processing-dependent properties of the carbon-depleted martensite should be considered in the optimization of Q&P processed steels.

The development of the quenching and partitioning (Q&P) process has prompted an interest in the process of isothermal transformation in presence of a pre-existing phase such as martensite. The presence of prior martensite is known to accelerate the overall kinetics of bainite formation, both in the 1-step and 2-step Q&P process. The underlying mechanisms behind this phenomenon are not fully understood. Also, the nature of the isothermal product (isothermal martensite and/or bainite) formed in presence of prior martensite seems to differ according to the thermodynamic and kinetic conditions. For certain thermodynamic conditions, depending on alloying, isothermal martensite may also form in the temperature range just above and below M_s. In the event that both bainite and isothermal martensite formation are thermodynamically allowed, the competition in kinetics determines the observed transformation product. The effect of martensite on the subsequent isothermal transformation is reviewed with a focus on the nature of the transformation products and kinetics. In that context, the kinetics of the isothermal transformation in presence of other prior phases such as polygonal ferrite and bainite are also compared and discussed, together with the possible mechanisms behind the acceleration of the transformation kinetics. Guidelines for further investigation are also proposed.