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.     

Microstructural basis for the effect of chromium on the strength and toughness of AF1410-based high performance steels

The variation in strength and Charpy impact toughness as a function of tempering temperature in the range of 200 ‡C to 650 ‡C was investigated in AF 1410 and AF 1410 + 1 pct Cr steels produced in a laboratory-scale, and a commercially produced AerMet 100 steel. The tensile test results showed that AF 1410 + 1 pct Cr had lower strength compared to AF 1410, while AerMet 100 had the highest strength of the three steels examined. Transmission electron microscopy (TEM) studies demonstrated that the strength variations among the steels can be attributed to differences in the matrix/carbide coherency strain and the volume fraction of the strengthening M₂C carbides. The toughness values of the three steels were comparable when tempered up to 424 ‡C. Tempering at and above 454 ‡C resulted in a relative enhancement of toughness in AF 1410 + 1 pct Cr steel compared to AF 1410. This toughening was attributed to the destabilization of cementite at lath and prior austenite boundaries and the formation of reverted austenite.     

Role of Tungsten in the Tempered Martensite Embrittlement of a Modified 9 Pct Cr Steel

The effect of tempering on the mechanical properties and fracture behavior of two 3 pct Co-modified 9 pct Cr steels with 2 and 3 wt pct W was examined. Both steels were ductile in tension tests and tough under impact tests in high-temperature tempered conditions. At T ≤ 923 K (650 °C), the addition of 1 wt pct W led to low toughness and pronounced embrittlement. The 9Cr2W steel was tough after low-temperature tempering up to 723 K (450 °C). At 798 K (525 °C), the decomposition of retained austenite induced the formation of discontinuous and continuous films of M₂₃C₆ carbides along boundaries in the 9Cr2W and the 9Cr3W steels, respectively, which led to tempered martensite embrittlement (TME). In the 9Cr2W steel, the discontinuous boundary films played a role of crack initiation sites, and the absorption energy was 24 J cm^?2. In the 9Cr3W steel, continuous films provided a fracture path along the boundaries of prior austenite grains (PAG) and interlath boundaries in addition that caused the drop of impact energy to 6 J cm^?2. Tempering at 1023 K (750 °C) completely eliminated TME by spheroidization and the growth of M₂₃C₆ carbides, and both steels exhibited high values of adsorbed energy of ≥230 J cm^?2. The addition of 1 wt pct W extended the temperature domain of TME up to 923 K (650 °C) through the formation of W segregations at boundaries that hindered the spheroidization of M₂₃C₆ carbides.     

Effects of Mn Addition on Tensile and Charpy Impact Properties in Austenitic Fe-Mn-C-Al-Based Steels for Cryogenic Applications

Effects of Mn addition (17, 19, and 22 wt pct) on tensile and Charpy impact properties in three austenitic Fe-Mn-C-Al-based steels were investigated at room and cryogenic temperatures in relation with deformation mechanisms. Tensile strength and elongation were not varied much with Mn content at room temperature, but abruptly decreased with decreasing Mn content at 77 K (?196 °C). Charpy impact energies at 273 K (0 °C) were higher than 200 J in the three steels, but rapidly dropped to 44 J at 77 K (?196 °C) in the 17Mn steel, while they were higher than 120 J in the 19Mn and 22Mn steels. Although the cryogenic-temperature stacking fault energies (SFEs) were lower by 30 to 50 pct than the room-temperature SFEs, the SFE of the 22Mn steel was situated in the TWinning-induced plasticity regime. In the 17Mn and 19Mn steels, however, α′-martensites were formed by the TRansformation-induced plasticity mechanism because of the low SFEs. EBSD analyses along with interrupted tensile tests at cryogenic temperature showed that the austenite was sufficiently deformed in the 19Mn steel even after the formation of α′-martensite, thereby leading to the high impact energy over 120 J.     

Tempered martensite embrittlement in SAE 4340 steel

The toughness of SAE 4340 steel with low (0.003 wt pct) and high (0.03 wt pct) phosphorus has been evaluated by Charpy V notch (CVN) impact and compact tension plane strain fracture toughness (K _1c) tests of specimens quenched and tempered up to 673 K (400°C). Both the high and low P steel showed the characteristic tempered martensite embrittlement (TME) plateau or trough in room temperature CVN impact toughness after tempering at temperatures between 473 K (200°C) and 673 K (400°C). The CVN energy absorbed by low P specimens after tempering at any temperature was always about 10 J higher than that of the high P specimens given the same heat treatment. Interlath carbide initiated cleavage across the martensite laths was identified as the mechanism of TME in the low P 4340 steel, while intergranular fracture, apparently due to a combination of P segregation and carbide formation at prior austenite grain boundaries, was associated with TME in the high P steel.K _IC values reflected TME in the high P steels but did not show TME in the low P steel, a result explained by the formation of a narrow zone of ductile fracture adjacent to the fatigue precrack during fracture toughness testing. The ductile fracture zone was attributed to the low rate of work hardening characteristic of martensitic steels tempered above 473 K (200°C).     

Effect of Retained Austenite on the Fracture Toughness of Quenching and Partitioning (Q&P)-Treated Sheet Steels

Fracture toughness K _IC was measured by double edge-notched tension (DENT) specimens with fatigue precracks on quenching and partitioning (Q&P)-treated high-strength (ultimate tensile strength [UTS] superior to 1200 MPa) sheet steels consisting of 4 to 10 vol pct of retained austenite. Crack extension force, G _IC, evaluated from the measured K _IC, is used to analyze the role of retained austenite in different fracture behavior. Meanwhile, G _IC is deduced by a constructed model based on energy absorption by martensite transformation (MT) behavior of retained austenite in Q&P-treated steels. The tendency of the change of two results is in good agreement. The Q&P-treated steel, quenched at 573 K (300 °C), then partitioned at 573 K (300 °C), holding for 60 seconds, has a fracture toughness of 74.1 MPa·m^1/2, which is 32 pct higher than quenching and tempering steel (55.9 MPa·m^1/2), and 16 pct higher than quenching and austempering (QAT) steel (63.8 MPa·m^1/2). MT is found to occur preferentially at the tips of extension cracks on less stable retained austenite, which further improves the toughness of Q&P steels; on the contrary, the MT that occurs at more stable retained austenite has a detrimental effect on toughness.     

Strength and toughness of Fe-10ni alloys containing C,Cr, Mo,and Co

The effects of C (0.10 to 0.20 pct), Cr (0 to 3 pct), Mo (0 to 2 pct), and Co (0 to 8 pct) on the yield strength, toughness (Charpy shelf energy), and tempering behavior of martensitic lONiCr-Mo-Co steels have been investigated. Variations in the carbon content between 0.10 and 0.20 pct result in yield strengths between 160 and 210 ksi (1.1 and 1.45 GN/m²) when these steels are tempered at 900° to 1000°F (480° to 540°C) for times of 1 to 100 h. These steels exhibit a secondary-hardening peak at 900° to 1000° F (480° to 540°C) where coarse Fe₃C carbides are gradually replaced by a fine, dislocation-nucleated dispersion of (Mo, Cr)₂C carbides. Maximum toughness at a given yield strength in these steels is only obtained when they are tempered for sufficiently long times so that the coarse Fe₃C carbides are completely dissolved. Molybdenum is primarily responsible for the secondary-hardening peak observed in these steels. However, chromium additions do result in lower secondaryhardening temperatures and promote coarsening of the secondary-hardening carbide. Best combinations of strength and toughness are obtained with steels containing 2 pct Cr and 1 pct Mo. Cobalt increases the yield strength of these steels over the entire tempering range and results in a higher secondary-hardening peak. This effect of cobalt is attributed to 1) a retardation in the rate of recovery of the dislocation substructure of the martensite, 2) the formation of a finer dispersion of secondary-hardening carbides, and 3) solid-solution strengthening. The finer dispersion of secondary-hardening carbides in steels containing cobalt is favored by the finer dislocation substructure in these steels since the (Mo, Cr)₂C carbide is dislocation-nucleated. This fine dispersion of (Mo, Cr)₂C carbide combined with the high nickel content accounts for the excellent combination of strength and toughness exhibited by these steels.     

Constitutive Modeling of the Mechanical Properties of V-added Medium Manganese TRIP Steel

In this study, medium Mn transformation-induced plasticity steel with the composition Fe-0.08 pct C-6.15 pct Mn-1.5 pct Si-2.0 pct Al-0.08 pct V was investigated. After intercritical annealing at 1013 K (740 °C), the steel contained coarse-grained ferrite and two ultrafine-grained (UFG) phases: ferrite and retained austenite. The material did not deform by localized Lüders band propagation: it did not suffer from this major problem as most UFG steels do. Localization of plastic flow was shown to be suppressed because of a combination of factors, including a bimodal grain size distribution, a multiphase microstructure, the presence of nanosized vanadium carbide precipitates, and the occurrence of the deformation-induced martensitic transformation of retained austenite. A constitutive model incorporating these effects was developed. The model was used to identify the factors which can lead to a further improvement of the mechanical properties of the UFG medium Mn TRIP steels.     

Effect of Mn Addition on Microstructural Modification and Cracking Behavior of Ferritic Light-Weight Steels

In the present study, effects of Mn addition on cracking phenomenon occurring during cold rolling of ferritic light-weight steels were clarified in relation to microstructural modification involving κ-carbide, austenite, and martensite. Four steels were fabricated by varying Mn contents of 3 to 12 wt pct, and edge areas of steel sheets containing 6 to 9 wt pct Mn were cracked during the cold rolling. The steels were basically composed of ferrite and austenite in a band shape, but a considerable amount of κ-carbide or martensite existed in the steels containing 3 to 6 wt pct Mn. Microstructural observation of the deformed region of fractured tensile specimens revealed that cracks which were initiated at ferrite/martensite interfacial κ-carbides readily propagated along ferrite/martensite interfaces or into martensite areas in the steel containing 6 wt pct Mn, thereby leading to the center or edge cracking during the cold rolling. In the steel containing 9 wt pct Mn, edge cracks were found in the final stage of cold rolling because of the formation of martensite by the strain-induced austenite to martensite transformation, whereas they were hardly formed in the steel containing 12 wt pct Mn. To prevent or minimize the cracking, it was recommended that the formation of martensite during the cooling from the hot rolling temperature or during the cold rolling should be suppressed, which could be achieved by the enhancement of thermal or mechanical stability of austenite with decreasing austenite grain size or increasing contents of austenite stabilizers.     

Interrelations of cooling rate,microstructure, and mechanical properties in four HSLA steels

The present study was carried out on four steels containing 0.1 pct C-1.5 pct Mn-0.003 pct B* in common, with additions of 1 pct Cr, 0.5 pct Mo, 0.25 pct Mo + 1 pct Cr, 0.2 pct Ti + 1 pct Cr. They were designated, accordingly, as Cr, Mo, Mo-Cr, and Cr-Ti steels. All the steels exhibited a complete lath martensite microstructure with thin interlaths of retained austenite (≈0.05 pct) in the quenched condition. The normalized microstructures, granular bainite, contained massive areas of ferrite and granules of bainite laths. Both microconstituents contained a fine dispersion of cementite particles (size ≈50 Å) together with high dislocation densities. A mechanism explaining their for-mation has been given. The Cr steel, due to its low hardenability, showed in addition polygonal ferrite in the neighborhood of the so-called M-A constituent (twinned martensite and/or austenite). The annealed microstructure (using a cooling rate of 0.033 °C s^?1) of the Cr steel consisted of coarse ferrite-pearlite. Addition of 0.2 pct Ti to the Cr steel markedly refined the structure, whereas an addition of 0.25 pct Mo altered the microstructure to ferrite-lower bainite. In the 0.5 pct Mo steel, polygonal ferrite was found to be completely missing. The mechanical properties of the four steels after quenching, normalizing, and annealing were investigatedvia hardness and tensile test mea-surements. An empirical equation, relating the ultimate tensile strength to the steel composition, for steels that had granular bainite microstructures in the normalized condition, was proposed. The fracture surfaces exhibited cleavage and variable-size dimples depending on the microstructure and steel composition.     

Effects of Oxides on Tensile and Charpy Impact Properties and Fracture Toughness in Heat Affected Zones of Oxide-Containing API X80 Linepipe Steels

This study is concerned with effects of complex oxides on acicular ferrite (AF) formation, tensile and Charpy impact properties, and fracture toughness in heat affected zones (HAZs) of oxide-containing API X80 linepipe steels. Three steels were fabricated by adding Mg and O₂ to form oxides, and various HAZ microstructures were obtained by conducting HAZ simulation tests under different heat inputs. The no. of oxides increased with increasing amount of Mg and O₂, while the volume fraction of AF present in the steel HAZs increased with increasing the no. of oxides. The strengths of the HAZ specimens were generally higher than those of the base metals because of the formation of hard microstructures of bainitic ferrite and granular bainite. When the total Charpy absorbed energy was divided into the fracture initiation and propagation energies, the fracture initiation energy was maintained constant at about 75 J at room temperature, irrespective of volume fraction of AF. The fracture propagation energy rapidly increased from 75 to 150 J and saturated when the volume fraction of AF exceeded 30 pct. At 253 K (?20 °C), the total absorbed energy increased with increasing volume fraction of AF, as the cleavage fracture was changed to the ductile fracture when the volume fraction of AF exceeded 45 pct. Thus, 45 vol pct of AF at least was needed to improve the Charpy impact energy, which could be achieved by forming a no. of oxides. The fracture toughness increased with increasing the no. of oxides because of the increased volume fraction of AF formed around oxides. The fracture toughness did not show a visible correlation with the Charpy absorbed energy at room temperature, because toughness properties obtained from these two toughness testing methods had different significations in view of fracture mechanics.     

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.     

Structure and mechanical properties of Fe-Cr-Mo-C alloys with and without boron

A study of the structure and mechanical properties of Fe-Cr-Mo-C martensitic steels with and without boron addition has been carried out. Nonconventional heat treatments have subsequently been designed to improve the mechanical properties of these steels. Boron has been known to be a very potent element in increasing the hardenability of steel, but its effect on structure and mechanical properties of quenched and tempered martensitic steels has not been clear. The present results show that the as-quenched structures of both steels consist mainly of dislocated martensite. In the boron-free steel, there are more lath boundary retained austenite films. The boron-treated steel shows higher strengths at all tempering temperatures but with lower Charpy V-notch impact energies. Both steels show tempered martensite embrittlement when tempered at 350 °C for 1 h. The properties above 500 °C tempering are significantly different in the two steels. While the boron-free steel shows a continuous increase in toughness when tempered above 500 °C, the boron-treated steel suffers a second drop in toughness at 600 °C tempering. Transmission electron microscopy studies show that in the 600 °C tempered boron-treated steel large, more or less continuous cementite films are present at the lath boundaries, which are probably responsible for the embrittlement. The differences in mechanical properties at tempering temperatures above 500 °C are rationalized in terms of the effect of boron-vacancy interactions on the recovery and recrystallization behavior of these steels. Although boron seems to impair room temperature impact toughness at low strength levels, it does not affect this property at high strength levels. By simple nonconventinal heat treatments of the present alloys, martensitic steels may be produced with quite good strength-toughness properties which are much superior to those of existing commercial ultra-high strength steels. It is also shown that very good combinations of strength and toughness can be obtained with as-quenched martensitic steels.     

Notch-Fatigue Properties of Advanced TRIP-Aided Bainitic Ferrite Steels

To develop a transformation-induced plasticity (TRIP)-aided bainitic ferrite steel (TBF steel) with high hardenability for a common rail of the next generation diesel engine, 0.2?pct C-1.5?pct Si-1.5?pct Mn-0.05?pct Nb TBF steels with different contents of Cr, Mo, and Ni were produced. The notch-fatigue strength of the TBF steels was investigated and was related to the microstructural and retained austenite characteristics. If Cr, Mo, and/or Ni were added to the base steel, then the steels achieved extremely higher notch-fatigue limits and lower notch sensitivity than base TBF steel and the conventional structural steels. This was mainly associated with (1) carbide-free and fine bainitic ferrite lath structure matrix without proeutectoid ferrite, (2) a large amount of fine metastable retained austenite, and (3) blocky martensite phase including retained austenite, which may suppress a fatigue crack initiation and propagation.     

Design of strong tough Fe/Mo/C martensitic steels and the effects of cobalt

The microstructures and mechanical properties of a series of vacuum melted Fe/(2 to 4) Mo/(0.2 to 0.4) C steels with and without cobalt have been investigated in the as-quenched fully martensitic condition and after quenching and tempering for 1 h at 673 K (400°C) and 873 K (600°C); austenitizing was done at 1473 K (1200°C) in argon. Very good strength and toughness properties were obtained with the Fe/2 Mo/0.4 C alloy in the as-quenched martensitic condition and this is attributed mainly to the absence of internal twinning. The slightly inferior toughness properties compared to Fe/Cr/C steels is attributed to the absence of interlath retained austenite. The two 0.4 pct carbon steels having low Mo contents had approximately one-half the amount of transformation twinning associated with the two 0.4 pct carbon steels having high Mo contents. The plane strain fracture toughness of the steels with less twinning was markedly superior to the toughness of those steels with similar alloy chemistry which had more heavily twinned microstructures. Experiments showed that additions of Co to a given Fe/Mo/C steel raised M_s but did not decrease twinning nor improve toughness. Molybdenum carbide particles were found in all specimens tempered at 673 K (400°C). The Fe/Mo/C system exhibits secondary hardening after tempering at 873 K (600°C). The precipitate is probably Mo₂C. This secondary hardening is associated with a reduction in toughness. Additions of Co to Fe/Mo/C steels inhibited or eliminated the secondary hardening effect normally observed. Toughness, however, did not improve and in fact decreased with Co additions.     

Fracture toughness of aisi M2 high-speed steel and corresponding matrix tool steel

The influence of microstructural variations on the fracture toughness of two tool steels with compositions 6 pct W-5 pct Mo-4 pct Cr-2 pct V-0.8 pct C (AISI M2 high-speed steel) and 2 pct W-2.75 pct Mo-4.5 pct Cr-1 pct V-0.5 pct C (VASCO-MA) was investigated. In the as-hardened condition, the M2 steel has a higher fracture toughness than the MA steel, although the latter steel is softer. In the tempered condition, MA is softer and has a higher fracture toughness than M2. When the hardening temperature is below 1095 °C (2000 °F), tempering of both steels causes embrittlement,i.e., a reduction of fracture toughness as well as hardness. The fracture toughness of both steels was enhanced by increasing the grain size. The steel samples with intercept grain size of 5 (average grain diameter of 30 microns) or coarser exhibit 2 to 3 MPa√m (2 to 3 ksi√in.) higher fracture toughness than samples with intercept grain size of 10 (average grain diameter of 15 microns) or finer. Tempering temperature has no effect on the fracture toughness of M2 and MA steels as long as the final tempered hardness of the steels is constant. Retained austenite has no influence on the fracture toughness of as-hardened MA steel, but a high content of retained austenite appears to raise the fracture toughness of as-hardened M2 steel. There is a temperature of austenitization for each tool steel at which the retained austenite content in the as-quenched samples is a maximum. The above described results were explained through changes in the microstructure and the fracture modes. CHONGMIN KIM, formerly with Climax Molybdenum Company of Michigan, Ann Arbor, MI.     

The effect of heat treatment on microstructure and cryogenic fracture properties in 5Ni and 9Ni steel

Heat treatments were utilized in 5Ni and 9Ni steel which resulted in the development of tempered microstructures which contained either no measurable retained austenite (<0.5 pct) or approximately 4 to 5 pct retained austenite as determined by X-ray diffraction. Microstructural observations coupled with the results of tensile testing indicated that the formation of retained austenite correlated with a decrease in carbon content of the matrix. Relative values ofK _IC at 77 K were estimated from slow bend precracked Charpy data using both the COD and equivalent energy measurements. In addition, Charpy impact properties at 77 K were determined. In the 9Ni alloy, optimum fracture toughness was achieved in specimens which contained retained austenite. This was attributed to changes in yield and work hardening behavior which accompanied the microstructural changes. In the 5Ni alloy, fracture toughness equivalent to that observed in the 9Ni alloy was developed in grain refined and tempered microstructures containing <0.5 pct retained austenite. A decrease in fracture toughness was observed in grain refined 5Ni specimens containing 3.8 pct retained austenite due to the premature onset of unstable cracking. This was attributed to the transformation of retained austenite to brittle martensite during deformation. It was concluded that the formation of thermally stable retained austenite is beneficial to the fracture toughness of Ni steels at 77 K as a result of austenite gettering carbon from the matrix during tempering. However, it was also concluded that the mechanical stability of the retained austenite is critical in achieving a favorable enhancement of cryogenic fracture toughness properties. Formerly with Union Carbide Corporation, Tarrytown, NY     

Thermally Stable Ni-rich Austenite Formed Utilizing Multistep Intercritical Heat Treatment in a Low-Carbon 10 Wt Pct Ni Martensitic Steel

Austenite reversion and its thermal stability attained during the transformation is key to enhanced toughness and blast resistance in transformation-induced-plasticity martensitic steels. We demonstrate that the thermal stability of Ni-stabilized austenite and kinetics of the transformation can be controlled by forming Ni-rich regions in proximity of pre-existing (retained) austenite. Atom probe tomography (APT) in conjunction with thermodynamic and kinetic modeling elucidates the role of Ni-rich regions in enhancing growth kinetics of thermally stable austenite, formed utilizing a multistep intercritical (Quench-Lamellarization-Tempering (QLT)-type) heat treatment for a low-carbon 10 wt pct Ni steel. Direct evidence of austenite formation is provided by dilatometry, and the volume fraction is quantified by synchrotron X-ray diffraction. The results indicate the growth of nm-thick austenite layers during the second intercritical tempering treatment (T-step) at 863 K (590 °C), with austenite retained from first intercritical treatment (L-step) at 923 K (650 °C) acting as a nucleation template. For the first time, the thermal stability of austenite is quantified with respect to its compositional evolution during the multistep intercritical treatment of these steels. Austenite compositions measured by APT are used in combination with the thermodynamic and kinetic approach formulated by Ghosh and Olson to assess thermal stability and predict the martensite-start temperature. This approach is particularly useful as empirical relations cannot be extrapolated for the highly Ni-enriched austenite investigated in the present study.     

Fracture toughness of CF8 castings at four kelvin

The first fracture toughness measurements for CF8 stainless steel castings in liquid helium at 4 K are reported. Single-phase (austenite) and duplex (austenite + δ-ferrite) castings were tested. On the basis of estimates from .J-integral data, the plane-strain fracture toughness(K _lc) of castings containing 3.2 to 14.5 pct δ-ferrite ranged from 84 to 179 MPa · m^1/2 at 4 K. In contrast, a fully austenitic casting (0 pct (δ-ferrite) exhibited aK _lc value of 331 MPa · m^-2, which is nearly equivalent to the toughness of a wrought AISI 304 stainless steel of a similar strength. Light and scanning electron microscopy studies indicate that the inferior toughness of castings containing ·-ferrite may be attributed to the brittleness of this body-centered-cubic phase at cryogenic temperatures and its distribution in the microstructure. The relative stability of the austenitic phase with respect to martensitic phase transformation may also play a significant role.     

Design of strong tough Fe/Mo/C martensitic steels and the effects of cobalt

The microstructures and mechanical properties of a series of vacuum melted Fe/(2 to 4) Mo/(0.2 to 0.4) C steels with and without cobalt have been investigated in the as-quenched fully martensitic condition and after quenching and tempering for 1 h at 673 K (400°C) and 873 K (600°C); austenitizing was done at 1473 K (1200°C) in argon. Very good strength and toughness properties were obtained with the Fe/2 Mo/0.4 C alloy in the as-quenched martensitic condition and this is attributed mainly to the absence of internal twinning. The slightly inferior toughness properties compared to Fe/Cr/C steels is attributed to the absence of interlath retained austenite. The two 0.4 pct carbon steels having low Mo contents had approximately one-half the amount of transformation twinning associated with the two 0.4 pct carbon steels having high Mo contents. The plane strain fracture toughness of the steels with less twinning was markedly superior to the toughness of those steels with similar alloy chemistry which had more heavily twinned microstructures. Experiments showed that additions of Co to a given Fe/Mo/C steel raisedM _S but did not decrease twinning nor improve toughness. Molybdenum carbide particles were found in all specimens tempered at 673 K (400°C). The Fe/Mo/C system exhibits secondary hardening after tempering at 873 K (600°C). The precipitate is probably Mo₂C. This secondary hardening is associated with a reduction in toughness. Additions of Co to Fe/Mo/C steels inhibited or eliminated the secondary hardening effect normally observed. Toughness, however, did not improve and in fact decreased with Co additions.