Characterization of the Carbon and Retained Austenite Distributions in Martensitic Medium Carbon, High Silicon Steel

The retained austenite content and carbon distribution in martensite were determined as a function of cooling rate and temper temperature in steel that contained 1.31 at. pct C, 3.2 at. pct Si, and 3.2 at. pct noniron metallic elements. Mössbauer spectroscopy, transmission electron microscopy (TEM), transmission synchrotron X-ray diffraction (XRD), and atom probe tomography were used for the microstructural analyses. The retained austenite content was an inverse, linear function of cooling rate between 25 and 560 K/s. The elevated Si content of 3.2 at. pct did not shift the start of austenite decomposition to higher tempering temperatures relative to SAE 4130 steel. The minimum tempering temperature for complete austenite decomposition was significantly higher (>650 °C) than for SAE 4130 steel (～300 °C). The tempering temperatures for the precipitation of transition carbides and cementite were significantly higher (>400 °C) than for carbon steels (100 °C to 200 °C and 200 °C to 350 °C), respectively. Approximately 90 pct of the carbon atoms were trapped in Cottrell atmospheres in the vicinity of the dislocation cores in dislocation tangles in the martensite matrix after cooling at 560 K/s and aging at 22 °C. The 3.2 at. pct Si content increased the upper temperature limit for stable carbon clusters to above 215 °C. Significant autotempering occurred during cooling at 25 K/s. The proportion of total carbon that segregated to the interlath austenite films decreased from 34 to 8 pct as the cooling rate increased from 25 to 560 K/s. Developing a model for the transfer of carbon from martensite to austenite during quenching should provide a means for calculating the retained austenite. The maximum carbon content in the austenite films was 6 to 7 at. pct, both in specimens cooled at 560 K/s and at 25 K/s. Approximately 6 to 7 at. pct carbon was sufficient to arrest the transformation of austenite to martensite. The chemical potential of carbon is the same in martensite that contains 0.5 to 1.0 at. pct carbon and in austenite that contains 6 to 7 at. pct carbon. There was no segregation of any substitutional elements.     

A Study of the Influence of Thermomechanical Controlled Processing on the Microstructure of Bainite in High Strength Plate Steel

Steels with compositions that are hot rolled and cooled to exhibit high strength and good toughness often require a bainitic microstructure. This is especially true for plate steels for linepipe applications where strengths in excess of 690 MPa (100 ksi) are needed in thicknesses between approximately 6 and 30 mm. To ensure adequate strength and toughness, the steels should have adequate hardenability (C. E. >0.50 and Pcm >0.20), and are thermomechanically controlled processed, i.e., controlled rolled, followed by interrupted direct quenching to below the Bs temperature of the pancaked austenite. Bainite formed in this way can be defined as a polyphase mixture comprised a matrix phase of bainitic ferrite plus a higher carbon second phase or micro-constituent which can be martensite, retained austenite, or cementite, depending on circumstances. This second feature is predominately martensite in IDQ steels. Unlike pearlite, where the ferrite and cementite form cooperatively at the same moving interface, the bainitic ferrite and MA form in sequence with falling temperature below the Bs temperature or with increasing isothermal holding time. Several studies have found that the mechanical properties may vary strongly for different types of bainite, i.e., different forms of bainitic ferrite and/or MA. Thermomechanical controlled processing (TMCP) has been shown to be an important way to control the microstructure and mechanical properties in low carbon, high strength steel. This is especially true in the case of bainite formation, where the complexity of the austenite-bainite transformation makes its control through disciplined processing especially important. In this study, a low carbon, high manganese steel containing niobium was investigated to better understand the effects of austenite conditioning and cooling rates on the bainitic phase transformation, i.e., the formation of bainitic ferrite plus MA. Specimens were compared after transformation from recrystallized, equiaxed austenite to deformed, pancaked austenite, which were followed by seven different cooling rates ranging between 0.5 K/s (0.5 °C/s) and 40 K/s (40 °C/s). The CCT curves showed that the transformation behaviors and temperatures varied with starting austenite microstructure and cooling rate, resulting in different final microstructures. The EBSD results and the thermodynamics and kinetics analyses show that in low carbon bainite, the nucleation rate is the key factor that affects the bainitic ferrite morphology, size, and orientation. However, the growth of bainite is also quite important since the bainitic ferrite laths apparently can coalesce or coarsen into larger units with slower cooling rates or longer isothermal holding time, causing a deterioration in toughness. This paper reviews the formation of bainite in this steel and describes and rationalizes the final microstructures observed, both in terms of not only formation but also for the expected influence on mechanical properties.     

Continuously Cooled Ultrafine Bainitic Steel with Excellent Strength–Elongation Combination

Serious efforts have been made to simultaneously improve the strength and ductility of steels for different applications. However, steel with the ultimate tensile strength (UTS) above 1200 MPa with minimum elongation of 20 pct is still difficult to produce. In the current work, an effort has been made to design such a steel that could be directly produced in any hot strip mill, after accelerated cooling on the runout table followed by coiling. Basically this steel consisted of C, Mn, Si, and Cr and the intended final microstructure at room temperature was about 80 pct carbide-free bainite and 20 pct retained austenite. The steel was exposed to a thermal treatment which is generally experienced by a hot strip coil. This newly developed steel possesses an UTS of minimum ~1370 MPa with minimum ~21 pct elongation. The combination of such encouraging mechanical properties can be primarily attributed to the formation of ultrafine bainite plates (~100 to 130 nm) and a high density of dislocations arising out of the bainitic transformation. The presence of sufficient quantity of retained austenite (minimum 21 pct) in the final microstructure could be the reason for the attainment of outstanding ductility values at such a high strength level.     

Carbon Redistribution and Carbide Precipitation in a High-Strength Low-Carbon HSLA-115 Steel Studied on a Nanoscale by Atom Probe Tomography

HSLA-115 is a newly developed Cu-bearing high-strength low-carbon martensitic steel for use in Naval structural applications. This research provides, for the first time, a comprehensive compositional analysis of carbon redistribution and associated complex phase transformations in an isothermal aging study of HSLA-115 at 823 K (550 °C). Specifically, we characterize carbon segregation at lath boundaries, grain-refining niobium carbonitrides, cementite, and secondary hardening M₂C carbides, in addition to copper precipitation, by 3D atom probe tomography (APT). Segregation of carbon (3 to 6 at. pct C) is observed at martensitic lath boundaries in the as-quenched and 0.12-hour aged microstructures. On further aging, carbon redistributes itself forming cementite and M₂C carbides. Niobium carbonitride precipitates do not dissolve during the austenitizing treatment and are inherited in the as-quenched and aged microstructures; these are characterized along with cementite by synchrotron X-ray diffraction and APT. Sub-nanometer-sized M₂C carbide precipitates are observed after the formation of Cu precipitates, co-located with the latter, indicating heterogeneous nucleation of M₂C. The temporal evolution of the composition and morphology of M₂C carbides at 823 K (550 °C) is described using APT; their precipitation kinetics is intertwined with Cu precipitates, affecting the bulk mechanical properties of HSLA-115. Phase compositions determined by APT are compared with computed compositions at thermodynamic equilibrium using ThermoCalc.     

Effect of phosphorus on the formation of retained austenite and mechanical properties in Si-containing low-carbon steel sheet

The effect of phosphorus and silicon on the formation of retained austenite has been investigated in a low-carbon steel cold rolled, intercritically annealed, and isothermally held in a temperature range of bainitic transformation followed by air cooling. The steel sheet containing phosphorus after final heat-treatment consisted of ferrite, retained austenite, and bainite or martensite. Phosphorus, especially in the presence of silicon, in steel was useful to assist the formation of retained austenite. Mechanical properties, such as tensile strength, uniform elongation, and the combination of tensile strength/ductility, were improved when phosphorus was increased up to 0.07 pct in 0.5 pct Si steel. This could be attributed to the strain-induced transformation of retained austenite during tensile deformation. Furthermore, two types of retained austenite were observed in P-containing steel. One is larger than about 1 μm in size and usually exists adjacent to bainite; the other one is of submicron size and usually exists in a ferrite matrix. High phosphorus content promotes the formation of stable (small size) austenites which are considered to be stabilized mainly by their small size effect and have a different formation mechanism from the coarser retained austenite in the lower P steels. The retained austenites of submicron size showed mechanical stability even after 10 pct deformation, suggesting that these small austenites have little effect on ductility. The 0.07 pct P-0.5 pct Si-1.5 pct Mn-0.12 pct C steel showed a high strength of 730 MPa and a total elongation of 36 pct.     

Evaluation of Carbon Partitioning in New Generation of Quench and Partitioning (Q&P) Steels

Quenching and partitioning (Q&P) and a novel combined process of hot straining (HS) and Q&P (HSQ&P) treatments have been applied to a TRIP-assisted steel in a Gleeble®3S50 thermomechanical simulator. The heat treatments involved intercritical annealing at 800 °C and a two-step Q&P heat treatment with a partitioning time of 100 seconds at 400 °C. The “optimum” quench temperature of 318 °C was selected according to the constrained carbon equilibrium (CCE) criterion. The effects of high-temperature deformation (isothermal and non-isothermal) on the carbon enrichment of austenite, carbide formation, and the strain-induced transformation to ferrite (SIT) mechanism were investigated. Carbon partitioning from supersaturated martensite into austenite and carbide precipitation were confirmed by means of atom probe tomography (APT) and scanning transmission electron microscopy (STEM). Austenite carbon enrichment was clearly observed in all specimens, and in the HSQ&P samples, it was significantly greater than in Q&P, suggesting an additional carbon partitioning to austenite from ferrite formed by the deformation-induced austenite-to-ferrite transformation (DIFT) phenomenon. By APT, the carbon accumulation at austenite/martensite interfaces was observed, with higher values for HSQ&P deformed isothermally (≈ 11 at. pct), when compared with non-isothermal HSQ&P (≈ 9.45 at. pct) and Q&P (≈ 7.6 at. pct). Moreover, a local Mn enrichment was observed in a ferrite/austenite interface, indicating ferrite growth under local equilibrium with negligible partitioning (LENP).

     

Mechanical Behavior of Carbide-free Medium Carbon Bainitic Steels

The effect of bainitic transformation time on the microstructure and mechanical properties was investigated in a steel containing 0.4 pct C-2.8 pct Mn-1.8 pct Si. The microstructure was characterized using optical and transmission electron microscopy; it consisted of bainitic ferrite, martensite, and retained austenite. The volume fraction of bainite increased from 0.4 for the shortest bainitic transformation time (30 minutes) to 0.9 at the longest time (120 minutes). The above microstructures exhibited an extended elasto-plastic transition leading to very high initial work-hardening rates. The work-hardening behavior was investigated in detail using strain-path reversals to measure the back stresses. These measurements point to a substantial kinematic hardening due to the mechanical contrast between the microstructural constituents. The onset of necking coincided with the saturation of kinematic hardening. Examination of the fracture surfaces indicated that the prior austenite grain boundaries play an important role in the fracture process.     

The Role of Silicon in the Solidification of High-Cr Cast Irons

This work analyzes the effect of different additions of silicon (0 to 5.0 pct) on the structure of a high-Chromium white cast iron, with chromium content of 16.8 pct and carbon 2.56 pct. The alloys were analyzed in both as-cast and heat-treated conditions. Casting was undertaken in metallic molds that yielded solidification rates faster than in commercial processes. Nevertheless, there was some degree of segregation of silicon; this segregation resulted in a refinement in the microstructure of the alloy. Silicon also generated a greater influence on the structure by destabilizing the austenitic matrix, and promoted greater precipitation of eutectic carbides. Above 3 pct silicon, pearlite formation occurred in preference to martensite. After the destabilization heat treatment, the matrix structure of the irons up to 3 pct Si consisted of secondary carbides in a martensitic matrix with some retained austenite; higher Si additions produced a ferritic matrix. The different as-cast and heat-treated microstructures were correlated with selected mechanical properties such as hardness, matrix microhardness, and fracture toughness. Silicon additions increased matrix microhardness in the as-cast conditions, but the opposite phenomenon occurred in the heat-treated conditions. Microhardness decreased as silicon content was increased. Bulk hardness showed the same behavior. Fracture toughness was observed to increase up to 2 pct Si, and then decreased for higher silicon contents. These results are discussed in terms of the effect of eutectic carbides’ size and the resulting matrix due to the silicon additions.     

Formation mechanism of bainitic ferrite in an Fe-2 Pct Si-0.6 Pct C alloy

The bainite transformation at 723 K in an Fe-2 pct Si-0.6 pct C alloy (mass pct) was investigated with transmission electron microscopy (TEM) and quantitative metallography to clarify the growth mechanism of the ferritic component of bainite. In early stages of transformation, the bainitic ferrite was carbide free. The laths of bainitic ferrite within a packet were parallel to one another and separated by carbon-enriched retained austenite. The average carbon concentration of the bainitic ferrite was estimated to be 0.19 mass pct at the lowest, indicating that the ferrite was highly supersaturated with respect to carbon. The laths did not thicken during the subsequent isothermal holding, although they were in contact with austenite of which the average carbon concentration was lower than the paraequilibrium value. In the later stage of transformation, large carbide plates formed in the austenite between the laths, resulting in the decrease in the carbon concentration of the austenite. Subsequently, the ferrite with a variant different from the initially formed ferrite in the packet was decomposed for the completion of transformation. The present results indicate that the bainitic ferrite develops by a displacive mechanism rather than a diffusional mechanism. Formerly Graduate Student, Kyoto University, Kyoto 606-01, Japan This article is based on a presentation made at the Pacific Rim Conference on the “Roles of Shear and Diffusion in the Formation of Plate-Shaped Transformation Products,” held December 18-22, 1992, in Kona, Hawaii, under the auspices of ASM INTERNATIONAL’S Phase Transformations Committee.     

Development of Multiphase Microstructure with Bainite, Martensite, and Retained Austenite in a Co-Containing Steel Through Quenching and Partitioning (Q&P) Treatment

The quenching and partitioning (Q&P) treatment of steel aims to produce a higher fraction of retained austenite by carbon partitioning from supersaturated martensite. Q&P studies done so far, relies on the basic concept of suppression of carbide formation by the addition of Si and/or Al. In the present study Q&P treatment is performed on a steel containing 0.32 C, 1.78 Mn, 0.64 Si, 1.75 Al, and 1.20 Co (all wt pct). A combination of 0.64 Si and 1.75 Al is chosen to suppress the carbide precipitation and therefore, to achieve carbon partitioning after quenching. Addition of Co along with Al is expected to accelerate the bainite transformation during Q&P treatment by increasing the driving force for transformation. The final aim is to develop a multiphase microstructure containing bainite, martensite, and the retained austenite and to study the effect of processing parameters (especially, quenching temperature and homogenization time) on the fraction and stability of retained austenite. A higher fraction of retained austenite (~13 pct) has indeed been achieved by Q&P treatment, compared to that obtained after direct-quenching (2.7 pct) or isothermal bainitic transformation (9.7 pct). Carbon partitioning during martensitic and bainitic transformations increased the stability of retained austenite.     

Third Generation 0.3C-4.0Mn Advanced High Strength Steels Through a Dual Stabilization Heat Treatment: Austenite Stabilization Through Paraequilibrium Carbon Partitioning

In excess of 30 vol. pct austenite can be retained in 0.3C-4.0Mn steels subjected to a dual stabilization heat treatment (DSHT) schedule—a five stage precisely controlled cooling schedule that is a variant of the quench and partition process. The temperature of the second quench (stage III) in the DSHT process plays an essential role in the retained austenite contents produced at carbon-partitioning temperatures of 723 K or 748 K (450° C or 475 °C) (stage IV). A thermodynamic model successfully predicted the retained austenite contents in heat-treated steels, particularly for a completely austenitized material. The microstructure and mechanical behavior of two heat-treated steels with similar levels of retained austenite (~30 vol. pct) were studied. Optimum properties—tensile strengths up to 1650 MPa and ~20 pct total elongation—were observed in a steel containing 0.3C-4.0Mn-2.1Si, 1.5 Al, and 0.5 Cr.     

Comprehensive Deformation Analysis of a Newly Designed Ni-Free Duplex Stainless Steel with Enhanced Plasticity by Optimizing Austenite Stability

A new metastable Ni-free duplex stainless steel has been designed with superior plasticity by optimizing austenite stability using thermodynamic calculations of stacking fault energy and with reference to literature findings. Several characterization methods comprising optical microscopy, magnetic phase measurements, X-ray diffraction (XRD) and electron backscattered diffraction were employed to study the plastic deformation behavior and to identify the operating plasticity mechanisms. The results obtained show that the newly designed duplex alloy exhibits some extraordinary mechanical properties, including an ultimate tensile strength of ~900 MPa and elongation to fracture of ~94 pct due to the synergistic effects of transformation-induced plasticity and twinning-induced plasticity. The deformation mechanism of austenite is complex and includes deformation banding, strain-induced martensite formation, and deformation-induced twinning, while the ferrite phase mainly deforms by dislocation slip. Texture analysis indicates that the Copper and Rotated Brass textures in austenite (FCC phase) and {001}〈110〉 texture in ferrite and martensite (BCC phases) are the main active components during tensile deformation. The predominance of these components is logically related to the strain-induced martensite and/or twin formation.     

Microstructure and Mechanical Properties of a Low-Carbon Mn-Si Multiphase Steel Based on Dynamic Transformation of Undercooled Austenite

The microstructure evolution of 0.20C-2.00Mn-2.00Si steel treated by the thermomechanical process to manufacture hot-rolled, transformation-induced plasticity (TRIP) steel based on dynamic transformation of undercooled austenite was investigated using a Gleeble 1500 (Dynamic Systems, Inc., Poestenkill, NY) hot simulation test machine in combination with light microscope (LM), scanning electron microscopy (SEM), and X-ray diffraction (XRD). The mechanical properties of this steel with different multiphase microstructures were also analyzed using room-temperature tensile tests. The results indicated that the multi-phase microstructures consisting of fine-grained ferrite with a size of 1–3 μm, bainite packets, and retained austenite and martensite were formed for the used steel by a thermo-mechanical process involving dynamic transformation of undercooled austenite, controlled cooling, isothermal bainite treatment and water-quenching. With the increase in the strain of hot deformation of undercooled austenite, the fraction of ferrite increased, that of bainite decreased, and that of martensite increased. At the same time, the fraction of retained austenite (RA), as well as the carbon content of RA, first increased and then decreased. For the used steel treated by such process, the tensile strength is about 1200 MPa with a total elongation of about 20 pct, and the product of tensile strength and total elongation can be up to 25,000 MPa × pct.     

Effect of alloying elements on the microstructure‐property relationship in thermomechanically processed C‐Mn‐Si TRIP steels

The effect of additions of Nb, Al and Mo to Fe‐C‐Mn‐Si TRIP steel on the final microstructure and mechanical properties after simulated thermomechanical processing (TMP) has been studied. The laboratory simulations of discontinuous cooling during TMP were performed using a hot rolling mill. All samples were characterised using optical microscopy and image analysis. The volume fraction of retained austenite was ascertained using a heat tinting technique and X‐ray diffraction measurements. Room temperature mechanical properties were determined by a tensile test. From this a comprehensive understanding of the structural aspect of the bainite transformation in these types of TRIP steels has been developed. The results have shown that the final microstructures of thermomechanically processed TRIP steels comprise ~ 50 % of polygonal ferrite, 7 ‐12 % of retained austenite, non‐carbide bainitic structure and martensite. All steels exhibited a good combination of ultimate tensile strength and total elongation. The microstructure‐property examination revealed the relationship between the composition of TRIP steels and their mechanical properties. It has been shown that the addition of Mo to the C‐Si‐Mn‐Nb TRIP steel increases the ultimate tensile strength up to 1020 MPa. The stability of the retained austenite of the Nb‐Mo steel was degraded, which led to a decrease in the elongation (24 %). The results have demonstrated that the addition of Al to C‐Si‐Mn‐Nb steel leads to a good combination of strength (~ 940 MPa) and elongation (~ 30 %) due to the formation of refined acicular ferrite and granular bainite structure with ~7 ‐ 8 % of stable retained austenite. Furthermore, it has been found that the addition of Al increases the volume fraction of bainitic ferrite laths. The investigations have shown an interesting result that, in the Nb‐Mo‐Al steel, Al has a more pronounced effect on the microstructure in comparison with Mo. It has been found that the bainitic structure of the Nb‐Mo‐Al steel appears to be more granular than in the Nb‐Mo steel. Moreover, the volume fraction of the retained austenite increased (12 %) with decreasing bainitic ferrite content. The results have demonstrated that this steel has the best mechanical properties (1100 MPa and 28 % elongation). It has been concluded that the combined effect of Nb, Mo, and Al addition on the dispersion of the bainite, martensite and retained austenite in the ferrite matrix and the morphology of these phases is different than effect of Nb, Mo and Al, separately.     

Nanoscale Analyses of High-Nickel Concentration Martensitic High-Strength Steels

Austenite reversion in martensitic steels is known to improve fracture toughness. This research focuses on characterizing mechanical properties and the microstructure of low-carbon, high-nickel steels containing 4.5 and 10 wt pct Ni after a QLT-type austenite reversion heat treatment: first, martensite is formed by quenching (Q) from a temperature in the single-phase austenite field, then austenite is precipitated by annealing in the upper part of the intercritical region in a lamellarization step (L), followed by a tempering (T) step at lower temperatures. For the 10 wt pct Ni steel, the tensile strength after the QLT heat treatment is 910 MPa (132 ksi) at 293 K (20 °C), and the Charpy V-notch impact toughness is 144 J (106 ft-lb) at 188.8 K (?84.4 °C, ?120 °F). For the 4.5 wt pct Ni steel, the tensile strength is 731 MPa (106 ksi) at 293 K (20 °C) and the impact toughness is 209 J (154 ft-lb) at 188.8 K (?84.4 °C, ?120 °F). Light optical microscopy, scanning electron and transmission electron microscopies, synchrotron X-ray diffraction, and local-electrode atom-probe tomography (APT) are utilized to determine the morphologies, volume fractions, and local chemical compositions of the precipitated phases with sub-nanometer spatial resolution. The austenite lamellae are up to 200 nm in thickness, and up to several micrometers in length. In addition to the expected partitioning of Ni to austenite, APT reveals a substantial segregation of Ni at the austenite/martensite interface with concentration maxima of 10 and 23 wt pct Ni for the austenite lamellae in the 4.5 and 10 wt pct Ni steels, respectively. Copper-rich and M₂C-type metal carbide precipitates were detected both at the austenite/martensite interface and within the bulk of the austenite lamellae. Thermodynamic phase stability, equilibrium compositions, and volume fractions are discussed in the context of Thermo-Calc calculations.     

Effect of Composition and Processing Parameters on the Formation of Nano-Bainite in Advanced High Strength Steels

The nano-bainitic microstructures were compared in a 0.79C-1.5Si-1.98Mn-0.24Mo-1.06Al (wt%) steel after isothermal heat-treatment and a Fe-0.2C-1.5Mn-1.2Si-0.3Mo-0.6Al-0.02Nb (wt%) steel after controlled thermomechanical processing.The microstructure for both steels consisted of bainite.The microstructural characteristics of bainite,such as the morphology of the nano-bainite and thicknesses of bainitic ferrite and retained austenite layers,as a function of steel composition and processing was studied using transmission electron microscopy (TEM).It was found that the nano-bainitic structure can be formed in the low alloy steel through thermomechanical processing.Atom probe tomography (APT) was employed as a powerful technique to determine local composition distributions in three dimensions with atomic resolution.The important conclusions from the APT research were that the carbon content of bainitic ferrite is higher than expected from paraequilibrium level of carbon in ferrite for both steels and that Fe-C clusters and fine particles are formed in the bainitic ferrite in both steels despite the high level of Si.     

Microstructure Evolution and Mechanical Behavior of a CMnSiAl TRIP Steel Subjected to Partial Austenitization Along with Quenching and Partitioning Treatment

The present study investigated the microstructure evolution and mechanical behavior in a low carbon CMnSiAl transformation-induced plasticity (TRIP) steel, which was subjected to a partial austenitization at 1183 K (910 °C) followed by one-step quenching and partitioning (Q&P) treatment at different isothermal holding temperatures of [533 K to 593 K (260 °C to 320 °C)]. This thermal treatment led to the formation of a multi-phase microstructure consisting of ferrite, tempered martensite, bainitic ferrite, fresh martensite, and retained austenite, offering a superior work-hardening behavior compared with the dual-phase microstructure (i.e., ferrite and martensite) formed after partial austenitization followed by water quenching. The carbon enrichment in retained austenite was related to not only the carbon partitioning during the isothermal holding process, but also the carbon enrichment during the partial austenitization and rapid cooling processes, which has broadened our knowledge of carbon partitioning mechanism in conventional Q&P process.     

Formation of Austenite During Intercritical Annealing of Dual-Phase Steels

The formation of austenite during intercritical annealing at temperatures between 740 and 900 °C was studied in a series of 1.5 pct manganese steels containing 0.06 to 0.20 pct carbon and with a ferrite-pearlite starting microstructure, typical of most dual-phase steels. Austenite formation was separated into three stages: (1) very rapid growth of austenite into pearlite until pearlite dissolution is complete; (2) slower growth of austenite into ferrite at a rate that is controlled by carbon diffusion in austenite at high temperatures (~85O °C), and by manganese diffusion in ferrite (or along grain boundaries) at low temperatures (~750 °C); and (3) very slow final equilibration of ferrite and austenite at a rate that is controlled by manganese diffusion in austenite. Diffusion models for the various steps were analyzed and compared with experimental results.     

Characterization of Transformation Stasis in Low-Carbon Steels Microalloyed with B and Mo

In the present study, bainite transformation kinetics was examined in low C-Mn steels with the addition of small amounts of B and Mo. This addition delays the onset of the bainite transformation. Mo addition causes transformation stasis at temperatures between 873 K and 823 K (600 °C and 550 °C) just below the bainite-start (B _s) temperature, resulting from an incomplete bainite transformation. Post-stasis transformation after a prolonged hold proceeds by the formation of ferrite with a low dislocation density, and in Mo-containing alloys, often the formation of carbides. The volume fraction at which the transformation stops is higher for lower carbon contents and lower transformation temperatures. By contrast, at 773 K (500 °C), the bainite transformation accompanying cementite precipitation occurs regardless of microalloying and is completed after shorter hold times. EDX measurement performed on the Mo-added 0.15 pct C alloy with aberration-corrected STEM revealed that segregation at the bainite/austenite interphase boundary is small for Mn and negligible for Mo in the early stages of stasis, which does not support the incomplete transformation mechanism based on the solute drag theory for the alloys used.     

A Novel Mo and Nb Microalloyed Medium Mn TRIP Steel with Maximal Ultimate Strength and Moderate Ductility

The multi-phase, metastable, and multi-scale (M³) constitution of a novel transformation-induced plasticity (TRIP) steel (Fe-0.17C-6.5Mn-1.1Al-0.22Mo-0.05Nb, wt pct) was designed through thermodynamic calculations combined with experimental analysis. In this study, Mo and Nb microalloying was used to control the fraction of retained austenite and its mechanical stability during tensile deformation and to improve the yield strength. Thermodynamic calculations were developed to determine the critical annealing temperature, at which a large fraction of retained austenite (~38 pct) would be obtained through the effects of solute enrichment. The experimental observation was in good agreement with the predicted results. According to the critical annealing temperature, such an ultrafine (<200 nm) M³, microstructure with optimum mechanical stability was successfully achieved. The results of this work demonstrated the superior performance with improved yield strength of 1020 to 1140 MPa and excellent ductility (>30 pct), as compared with other TRIP steels. Both angle-selective backscatter and electron backscatter diffraction techniques were employed to interpret the transformation from the deformed martensitic laths to the ultrafine austenite and ferrite duplex structure.