Retained Austenite Transformation during Heat Treatment of a 5 Wt Pct Cr Cold Work Tool Steel

Retained austenite transformation was studied for a 5 wt pct Cr cold work tool steel tempered at 798 K and 873 K (525 °C and 600 °C) followed by cooling to room temperature. Tempering cycles with variations in holding times were conducted to observe the mechanisms involved. Phase transformations were studied with dilatometry, and the resulting microstructures were characterized with X-ray diffraction and scanning electron microscopy. Tempering treatments at 798 K (525 °C) resulted in retained austenite transformation to martensite on cooling. The martensite start (M _s ) and martensite finish (M _f ) temperatures increased with longer holding times at tempering temperature. At the same time, the lattice parameter of retained austenite decreased. Calculations from the M _s temperatures and lattice parameters suggested that there was a decrease in carbon content of retained austenite as a result of precipitation of carbides prior to transformation. This was in agreement with the resulting microstructure and the contraction of the specimen during tempering, as observed by dilatometry. Tempering at 873 K (600 °C) resulted in precipitation of carbides in retained austenite followed by transformation to ferrite and carbides. This was further supported by the initial contraction and later expansion of the dilatometry specimen, the resulting microstructure, and the absence of any phase transformation on cooling from the tempering treatment. It was concluded that there are two mechanisms of retained austenite transformation occurring depending on tempering temperature and time. This was found useful in understanding the standard tempering treatment, and suggestions regarding alternative tempering treatments are discussed.     

In Situ Thermo-magnetic Investigation of the Austenitic Phase During Tempering of a 13Cr6Ni2Mo Supermartensitic Stainless Steel

The formation of austenite during tempering of a 13Cr6Ni2Mo supermartensitic stainless steel (X2CrNiMoV13-5-2) was investigated using an in situ thermo-magnetic technique to establish the kinetics of the martensite to austenite transformation and the stability of austenite. The austenite fraction was obtained from in situ magnetization measurements. It was found that during heating to the tempering temperature 1 to 2 vol pct of austenite, retained during quenching after the austenitization treatment, decomposed between 623 K and 753 K (350 °C and 480 °C). The activation energy for martensite to austenite transformation was found by JMAK-fitting to be 233 kJ/mol. This value is similar to the activation energy for Ni and Mn diffusion in iron and supports the assumption that partitioning of Ni and Mn to austenite are mainly rate determining for the austenite formation during tempering. This also indicates that the stability of austenite during cooling after tempering depends on these elements. With increasing tempering temperature the thermal stability of austenite is decreasing due to the lower concentrations of austenite-stabilizing elements in the increased fraction of austenite. After cooling from the tempering temperature the retained austenite was further partially decomposed during holding at room temperature. This appears to be related to previous martensite formation during cooling.     

Microstructure-strength relations in a hardenable stainless steel with 16 pct Cr, 1.5 pct Mo,and 5 pct Ni

Metallographic studies have been conducted on a 0.024 pct C-16 pct Cr-1.5 pct Mo-5 pct Ni stainless steel to study the phase reactions associated with heat treatments and investigate the strengthening mechanisms of the steel. In the normalized condition, air cooled from 1010 °C, the microstructure consists of 20 pct ferrite and 80 pct martensite. Tempering in a temperature range between 500 and 600 °C results in a gradual transformation of martensite to a fine mixture of ferrite and austenite. At higher tempering temperatures, between 600 and 800 °C, progressively larger quantities of austenite form and are converted during cooling to proportionally increasing amounts of fresh martensite. The amount of retained austenite in the microstructure is reduced to zero at 800 °C, and the microstructure contains 65 pct re-formed martensite and 35 pct total ferrite. Chromium rich M₂₃C₆ carbides precipitate in the single tempered microstructures. The principal strengthening is produced by the presence of martensite in the microstructure. Additional strengthening is provided by a second tempering treatment at 400 °C due to the precipitation of ultrafine (Cr, Mo) (C,N) particles in the ferrite.     

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.     

The mechanical stability of austenite and cryogenic toughness of ferritic Fe-Mn-AI Alloys

In an attempt to understand the role of retained austenite on the cryogenic toughness of a ferritic Fe-Mn-AI steel, the mechanical stability of austenite during cold rolling at room temperature and tensile deformation at ambient and liquid nitrogen temperature was investigated, and the microstructure of strain-induced transformation products was observed by transmission electron microscopy (TEM). The volume fraction of austenite increased with increasing tempering time and reached 54 pct after 650 °C, 1-hour tempering and 36 pct after 550 °C, 16-hour tempering. Saturation Charpy impact values at liquid nitrogen temperature were increased with decreasing tempering temperature, from 105 J after 650 °C tempering to 220 J after 550 °C tempering. The room-temperature stability of austenite varied significantly according to the(α + γ) region tempering temperature;i.e., in 650 °C tempered specimens, 80 to 90 pct of austenite were transformed to lath martensite, while in 550 °C tempered specimens, austenite remained untransformed after 50 pct cold reductions. After tensile fracture (35 pct tensile strain) at -196 °C, no retained austenite was observed in 650 °C tempered specimens, while 16 pct of austenite and 6 pct of e-martensite were observed in 550 °C tempered specimens. Considering the high volume fractions and high mechanical stability of austenite, the crack blunting model seems highly applicable for improved cryogenic toughness in 550 °C tempered steel. Other possible toughening mechanisms were also discussed. Formerly Graduate Student, Seoul National University.     

Effects of Heating and Cooling Rates on Phase Transformations in 10 Wt Pct Ni Steel and Their Application to Gas Tungsten Arc Welding

10 wt pct Ni steel is a high-strength steel that possesses good ballistic resistance from the deformation induced transformation of austenite to martensite, known as the transformation-induced-plasticity effect. The effects of rapid heating and cooling rates associated with welding thermal cycles on the phase transformations and microstructures, specifically in the heat-affected zone, were determined using dilatometry, microhardness, and microstructural characterization. Heating rate experiments demonstrate that the Ac₃ temperature is dependent on heating rate, varying from 1094 K (821 °C) at a heating rate of 1 °C/s to 1324 K (1051 °C) at a heating rate of 1830 °C/s. A continuous cooling transformation diagram produced for 10 wt pct Ni steel reveals that martensite will form over a wide range of cooling rates, which reflects a very high hardenability of this alloy. These results were applied to a single pass, autogenous, gas tungsten arc weld. The diffusion of nickel from regions of austenite to martensite during the welding thermal cycle manifests itself in a muddled, rod-like lath martensitic microstructure. The results of these studies show that the nickel enrichment of the austenite in 10 wt pct Ni steel plays a critical role in phase transformations during welding.     

Warm Formability of 0.2 Pct C-1.5 Pct Si-5 Pct Mn Transformation-Induced Plasticity-Aided Steel

The warm stretch formability and flangeability of 0.2 pct C-1.5 pct Si-5 pct Mn transformation-induced plasticity-aided sheet steel with annealed martensite matrix were investigated for automotive applications. Both formabilities were enhanced by warm forming at peak temperatures of 423 K to 573 K and 423 K to 523 K (150 °C to 300 °C and 150 °C to 250 °C), respectively. The superior warm formabilities were mainly due to the stabilization of a large amount of retained austenite by warm forming and the consequent considerably suppressed void growth at the interface between the matrix and transformed martensite, despite there being large hole punching damage for the stretch flangeability. High peak temperatures for stretch formability and flangeability were associated with apparently increased M _S of the retained austenite resulting from the increased mean normal stress on stretch forming and hole expansion.     

A study of the early stages of tempering of iron-carbon martensites by atom probe field ion microscopy

The redistribution of carbon atoms during the early stages of ageing and tempering of iron-carbon martensites has previously been studied only by indirect methods. The computer-controlled atom probe field ion microscope permits the direct, quantitative determination of carbon concentrations at the atomic level, and thus all the stages of the martensite decomposition process become amenable to direct study. Analyses of a low-carbon martensite, Fe-1.0 at. pct C, (Fe-0.21 wt pct C), water quenched and tempered for 10 min at 150 °C, showed a matrix carbon content of only 0.14 at. pct. Analysis of a 2 nm diam area centered on a lath boundary showed a local concentration of 2.01 at. pct C. There is some evidence that this carbon level is associated with the presence of a thin film of retained austenite at the boundary. In the case of a higher carbon martensite, Fe-0.64 at. pct Mn, 3.47 at. pct C, (Fe-0.65 wt pct Mn-0.78 wt pct C) water quenched and aged for approximately 24 h at room temperature, analysis of twinned regions showed a matrix carbon level of 2.7 at. pct and a concentration enrichment to 6.9 at. pct in a region 2 nm diam, centered on the coherent twin interface. Assuming the segregated carbon to be located in a single atomic layer at the twin interface, this result indicates that a carbon concentration of 24 at. pct exists locally at the boundary. These results appear to be the first direct demonstration of the segregation of carbon atoms to lattice defects in carbon martensites. Tempering of the higher carbon martensite for 1 h at 160 °C produced further segregation of carbon to the region of twin interfaces. The matrix carbon content fell to 1.5 at. pct and the average carbon content over a 2 nm diam region at the interface rose to 8.7 at. pct. The width of the carbon segregated regions also increased, which seems to imply that incipient carbide precipitation in the plane of the twin boundaries is occurring at this stage of the tempering process. Formerly with the Department of Metallurgy and Science of Materials, University of Oxford     

Retained Austenite and Tempered Martensite Embrittlement in Medium Carbon Steels

Electron microscopy, diffraction and microanalysis, X-ray diffraction, and auger spectroscopy have been used to study quenched and quenched and tempered 0.3 pct carbon low alloy steels. Some in situ fracture studies were also carried out in a high voltage electron microscope. Tempered martensite embrittlement (TME) is shown to arise primarily as a microstructural constraint associated with decomposition of interlath retained austenite into M₃C films upon tempering in the range of 250 °C to 400 °C. In addition, intralath Widmanstätten Fe₃C forms from epsilon carbide. The fracture is transgranular with respect to prior austenite. The situation is analogous to that in upper bainite. This TME failure is different from temper embrittlement (TE) which occurs at higher tempering temperatures (approximately 500 °C), and is not a microstructural effect but rather due to impurity segregation (principally sulfur in the present work) to prior austenite grain boundaries leading to intergranular fracture along those boundaries. Both failures can occur in the same steels, depending on the tempering conditions.     

In situ X-Ray Diffraction Analysis of Carbon Partitioning During Quenching of Low Carbon Steel

In situ X-ray diffraction investigations of phase transformations during quenching of low carbon steel were performed at the European Synchrotron Radiation Facility (ESRF, Grenoble, France) at beamline ID11. A dynamic stabilization of the retained austenite during cooling below martensite start was identified, resulting in an amount of retained austenite of approximately 4?vol pct. The reason for this dynamic stabilization is a carbon partitioning occurring directly during quenching from martensite (and a small amount of bainite) into retained austenite. A carbon content above 0.5?mass pct was determined in the retained austenite, while the nominal carbon content of the steel was 0.2?mass pct. The martensitic transformation kinetic was compared with the models of Koistinen-Marburger and a modification proposed by Wildau. The analysis revealed that the Koistinen-Marburger equation does not provide reliable kinetic modeling for the described experiments, while the modification of Wildau well describes the transformation kinetic.     

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.     

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.     

Retained Austenite Decomposition and Carbide Formation During Tempering a Hot-Work Tool Steel X38CrMoV5-1 Studied by Dilatometry and Atom Probe Tomography

The microstructural development of a hot-work tool steel X38CrMoV5-1 during continuous heating to tempering temperature has been investigated with the focus on the decomposition of retained austenite (Stage II) and carbide formation (Stages III and IV). Investigations have been carried out after heating to 673.15?K, 773.15?K, 883.15?K (400?°C, 500?°C, 610?°C) and after a dwell time of 600?seconds at 883.15?K (610?°C). Dilatometry and atom probe tomography were used to identify tempering reactions. A distinctive reaction takes place between 723.15?K and 823.15?K (450?°C and 550?°C) which is determined to be the formation of M₃C from transition carbides. Stage II could be evidenced with the atom probe results and indirectly with dilatometry, indicating the formation of new martensite during cooling. Retained austenite decomposition starts with the precipitation of alloy carbides formed from nanometric interlath retained austenite films which are laminary arranged and cause a reduction of the carbon content within the retained austenite. Preceding enrichment of substitutes at the matrix/carbide interface in the early stages of Cr₇C₃ alloy carbide formation could be visualised on the basis of coarse M₃C carbides within the matrix. Atom probe tomography has been found to be very useful to complement dilatational experiments in order to characterise and identify microstructural changes.     

Tempering of Mn and Mn-Si-V Dual-Phase Steels

Changes in the yield behavior, strength, and ductility of a Mn and a Mn-Si-V dual-phase (ferrite-martensite) steel were investigated after tempering one hour at 200 to 600 °C. The change in yield behavior was complex in both steels with the yield strength first increasing and then decreasing as the tempering temperature was increased. This complex behavior is attributed to a combination of factors including carbon segregation to dislocations, a return of discontinuous yielding, and the relief of residual stresses. In contrast, the tensile strength decreased continuously as the tempering temperature was increased in a manner that could be predicted from the change in hardness of the martensite phase using a simple composite strengthening model. The initial tensile ductility (total elongation) of the Mn-Si-V steel was much greater than that of the Mn steel. However, upon tempering up to 400 °C, the ductility of the Mn-Si-V decreased whereas that of the Mn steel increased. As a result, both steels had similar ductilities after tempering at 400 °C or higher temperatures. These results are attributed to the larger amounts of retained austenite in the Mn-Si-V steel (9 pct) compared to the Mn steel (3 pct) and its contribution to tensile ductility by transforming to martensite during plastic straining. Upon tempering at 400 °C, the retained austenite decomposes to bainite and its contribution to tensile ductility is eliminated.     

Chi-Carbide in Tempered High Carbon Martensite

Martensite in an Fe-1.22C alloy was tempered at 523, 573, and 623 K and examined by transmission electron microscopy (TEM) and Mössbauer effect spectroscopy (MES) to identify the morphology and type of carbide formed at the beginning of the third stage of tempering. Carbides formed in three morphologies: on twins within the martensite plates, in the matrix of twin-free areas of the martensite plates, and along the interfaces of the martensite plates. Chi-carbide (χ), as identified by selected area diffraction (SAD), was associated with each carbide morphology in specimens tempered at 573 K. Cementite (θ) together with chi-carbide was observed in specimens tempered at 623 K. Small amounts (about 2 pct) of retained austenite were observed by MES of specimens tempered at 523 K. The transformation of the 25 pct retained austenite in as-quenched specimens was related to the χ-carbide formed at the martensite plate interfaces during tempering. The MES results also show the presence of χ-carbide in the specimen tempered at 523 K and yields parameters indicative of a mixture of χ and θ carbides for the specimens tempered at 573 K and 623 K. MES measurements of the magnetic transition temperatures of the carbides show diffuse transitions but suggest thatχ is the dominant carbide in the tempering temperature range examined.     

Heat Treatment of Thixo-Formed Hypereutectic X210CrW12 Tool Steel

Steel is a particularly challenging material to semisolid process because of the high temperatures involved and the potential for surface oxidation. Hot-rolled X210CrW12 tool steel was applied as a feedstock for thixoforming. The samples were heated up to 1525?K (1250?°C) to obtain 30?pct of the liquid phase. They were pressed in the semisolid state into a die preheated up to 473?K (200?°C) using a device based on a high-pressure die casting machine. As a result, a series of main bucket tooth thixo-casts for a mining combine was obtained. The microstructure of the thixo-cast consisted of austenite globular grains (average grain size 46 ??m) surrounded by a eutectic mixture (ferrite, austenite, and M₇C₃ carbides). The average hardness of primary austenite grains was 470?HV_0.02 and that of eutectic 551?HV_0.02. The X-ray analysis confirmed the presence of 11.8?pct ??-Fe, 82.4?pct ??-Fe, and 5.8?pct M₇C₃ carbides in the thixo-cast samples. Thermal and dilatometric effects were registered in the solid state, and the analysis of curves enabled the determination of characteristic temperatures of heat treatment: 503?K, 598?K, 693?K, 798?K, 828?K, 903?K, and 953?K (230?°C, 325?°C, 420?°C, 525?°C, 555?°C, 630?°C, 680?°C). The thixo-casts were annealed at these temperatures for 2?hours. During annealing in the temperature range 503?K to 693?K (230?°C to 420?°C), the hardness of primary globular grains continuously decreased down to 385HV_0.02. The X-ray diffraction showed a slight shift of peaks responsible for the tension release. Moreover, after the treatment at 693?K (420?°C), an additional peak from precipitated carbides was observed in the X-ray diffraction. Thin plates of perlite (average hardness 820?HV_0.02) with carbide precipitates appeared at the boundaries of globular grains at 798?K (525?°C). They occupied 17?pct of the grain area. Plates of martensite were found in the center of grains, while the retained austenite was observed among them (average hardness of center grains was 512?HV_0.02). A nearly complete decomposition of metastable austenite was achieved after tempering at 828?K (555?°C) due to prevailing lamellar pearlite structure starting at grain boundaries and the martensite located in the center of the grains. The X-ray analysis confirmed the presence of 3.4?pct ??-Fe, 84.6?pct ??-Fe, and 12?pct M₇C₃ carbides. The dilatometric analysis showed that the transformation of metastable austenite into martensite took place during cooling from 828?K (555?°C). The additional annealing at 523?K (250?°C) for 2?hours after heat treatment at 828?K (555?°C) caused the precipitation of carbides from the martensite. After tempering at 903?K (630?°C), the thixo-cast microstructure showed globular grains consisting mainly of thick lamellar perlite of the average hardness 555?HV_0.02.     

Excess Solute Carbon and Retained Tetragonality in Tempered Fe-0.6C-1Mn Martensite and the Effect of Silicon Addition

The tetragonality and carbon distribution in tempered Fe-0.6C-1Mn martensite were investigated by X-ray diffraction and atom probe tomography to elucidate strain relaxation in the tetragonal lattice during tempering and its relationship with the solubility of excess carbon in martensite. Even though tetragonality (c/a) decreased with an increase in the tempering temperature, it persisted at low levels up to 400 °C. Si addition suppressed the decrease in tetragonality at 400 °C by inhibiting recovery in the dislocated matrix. Such persistence implies that dislocation migration is crucial for the complete release of tetragonal lattice strain at such a temperature, in addition to the decrease in the amount of solute carbon in martensite. A low level of tetragonality was observed for martensite containing carbon in the solid solution below the critical value of ~ 0.2 mass pct, at which a bcc structure was predicted. The amount of solute carbon after tempering was linearly correlated with tetragonality in the solute carbon content range of 0.07 to 0.6 mass pct, and the correlation coefficient was similar to those for as-quenched auto-tempered martensite and bainitic ferrite; these results indicate that the amount of excess carbon is simply determined by the amount of tetragonal lattice distortions remaining after carbide precipitation and recovery.

     

Effects of Pre-tempering on Intercritical Annealing in Fe-2Mn-0.3C Alloy

As-quenched martensite was pre-tempered at 623 K and 923 K (350 °C and 650 °C), and then it reverted to austenite by intercritical annealing at 998 K (725 °C) in a Fe-2Mn-0.3C alloy. Pre-tempering at 623 K (350 °C) accelerates austenite formation, while pre-tempering at 923 K (650 °C) significantly retards it. It is proposed that austenite nucleation is accelerated by increasing the number density and particle size of cementite during tempering, whereas austenite growth is retarded by Mn enrichment in cementite during tempering at high temperature, leading to opposite effects of pre-tempering on reversion kinetics.     

Impact of Si on Microstructure and Mechanical Properties of 22MnB5 Hot Stamping Steel Treated by Quenching & Partitioning (Q&P)

Based on 22MnB5 hot stamping steel, three model alloys containing 0.5, 0.8, and 1.5 wt pct Si were produced, heat treated by quenching and partitioning (Q&P), and characterized. Aided by DICTRA calculations, the thermal Q&P cycles were designed to fit into industrial hot stamping by keeping partitioning times ≤ 30 seconds. As expected, Si increased the amount of retained austenite (RA) stabilized after final cooling. However, for the intermediate Si alloy the heat treatment exerted a particularly pronounced influence with an RA content three times as high for the one-step process compared to the two-step process. It appeared that 0.8 wt pct Si sufficed to suppress direct cementite formation from within martensite laths but did not sufficiently stabilize carbon-soaked RA at higher temperatures. Tensile and bending tests showed strongly diverging effects of austenite on ductility. Total elongation improved consistently with increasing RA content independently from its carbon content. In contrast, the bending angle was not impacted by high-carbon RA but deteriorated almost linearly with the amount of low-carbon RA.     

Tempering characteristics of a vanadium containing dual phase steel

Dual phase steels are characterized by a microstructure consisting of ferrite, martensite, retained austenite, and/or lower bainite. This microstructure can be altered by tempering with accompanying changes in mechanical properties. This paper examines such changes produced in a vanadium bearing dual phase steel upon tempering below 500 °C. The steel mechanical properties were minimally affected on tempering below 200 °C; however, a simultaneous reduction in uniform elongation and tensile strength occurred upon tempering above 400 °C. The large amount of retained austenite (≅10 vol pct) observed in the as-received steel was found to be essentially stable to tempering below 300 °C. On tempering above 400 °C, most of the retained austenite decomposed to either upper bainite (at 400 °C) or a mixture of upper bainite and ferrite-carbide aggregate formed by an interphase precipitation mechanism (at 500 °C). In addition, tempering at 400 °C led to fine precipitation in the retained ferrite. The observed mechanical properties were correlated with these microstructural changes. It was concluded that the observed decrease in uniform elongation upon tempering above 400 °C is primarily the consequence of the decomposition of retained austenite and the resulting loss of transformation induced plasticity (TRIP) as a contributing mechanism to the strain hardening of the steel. B. V. N. RAO, formerly Senior Research Engineer, Analytical Chemistry Department, General Motors Research Laboratories