Effect of carbon concentration on precipitation behavior of M<Subscript>23</Subscript>C<Subscript>6</Subscript> carbides and MX carbonitrides in martensitic 9Cr steel during heat treatment

The distributions and precipitated amounts of M₂₃C₆ carbides and MX-type carbonitrides with decreasing carbon content from 0.16 to 0.002 mass pct in 9Cr-3W steel, which is used as a heat-resistant steel, has been investigated. The microstructures of the steels are observed to be martensite. Distributions of precipitates differ greatly among the steels depending on carbon concentration. In the steels containing carbon at levels above 0.05 pct, M₂₃C₆ carbides precipitate along boundaries and fine MX carbonitrides precipitate mainly in the matrix after tempering. In 0.002 pct C steel, there are no M₂₃C₆ carbide precipitates, and instead, fine MX with sizes of 2 to 20 nm precipitate densely along boundaries. In 0.02 pct C steel, a small amount of M₂₃C₆ carbides precipitate, but the sizes are quite large and the main precipitates along boundaries are MX, as with 0.002 pct C steel. A combination of the removal of any carbide whose size is much larger than that of MX-type nitrides, and the fine distributions of MX-type nitrides along boundaries, is significantly effective for the stabilization of a variety of boundaries in the martensitic 9Cr steel.     

Study of Property Degradation of T23 Heat‐resistant Steel based on Microstructural Evolution during Creep

In order to study the microstructural evolution and the effect on property degradation of T23 heat‐resistance steel (2.25Cr‐1.6W‐V‐Nb‐B‐N) during creep, creep rupture specimens were investigated at 823K, 873K and 923K. The microstuctural evolution was examined by optical, scanning and transmission electron microscopy. It has been noted that the creep property degradation of T23 is related to the decrease of dislocation density due to the recovery and recrystallization of the bainitic ferrite matrix and the martensite in the carbon‐rich islands, the coarsening of M₂₃C₆ carbides, and even the transformation from M₂₃C₆ to M₆C. Coarsening of M₂₃C₆ is the dominating effect during short‐term creep whereas recovery and recrystallization is the key factor for long‐term creep. Property degradation is advanced at higher temperature due to the quicker recovery and recrystallization.     

Effect of M3C on the Precipitation Behavior of M23C6 Phase during Early Stage of Tempering in T91 Ferritic Steel

Tempered martensitic structure is the service condition of T91 ferritic steel after adopting the austenitizing followed by tempering. Needle‐like M₃C particles are precipitated during air cooling after austenization, while the precipitation of M₃C is suppressed during the water cooling. The effect of existence of M₃C on the precipitation behaviors of M₂₃C₆ during the early stage of tempering, as nucleation site, number density and size distribution, was investigated by means of TEM observation. The TEM results indicate that, upon the same tempering time, the size of M₂₃C₆ is smaller and its number density is higher in the sample pre‐existing M₃C than in the sample without M₃C. This can be explained that existence of M₃C results in more M₂₃C₆ precipitates forming inside of grain, where a relatively low self‐diffusion coefficient of alloy element leads to M₂₃C₆ hardly coarsening. However, with the prolongation of tempering time, this effect becomes weaken. Microhardness results indicate that the existence of M₃C phase results in the increase of hardness after tempering due to the precipitation of finer and denser M₂₃C₆ particles.     

Effect of fine precipitation and subsequent coarsening of Fe<Subscript>2</Subscript>W laves phase on the creep deformation behavior of tempered martensitic 9Cr-W steels

The effect of fine precipitation and subsequent coarsening of Fe₂W Laves phase on the creep deformation behavior was investigated for simple 9Cr-W steels containing 0, 1, 2, and 4 wt pct W. After tempering, the specimens were subjected to creep tests at 823, 873, and 923 K for up to 15,000 hours. The precipitation of Fe₂W Laves phase takes place during creep at boundaries from the supersaturated solid solution of the high-W steels, the 9Cr-2W and 9Cr-4W steels, but not in the low-W steels, the 9Cr-0W and 9Cr-1W steels. The fine precipitation of Fe₂W Laves phase decreases the creep rate in the primary or transient creep region, while the subsequent large coarsening of Fe₂W Laves phase reduces the precipitation strengthening and promotes the acceleration of creep rate in the tertiary or acceleration creep region after reaching a minimum creep rate. The change in shape of creep rate curves with stress and temperature is explained by taking fine precipitation and subsequent coarsening of Fe₂W Laves phase into account.     

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.     

Phase transformations during tempering of the Fe-15Cr-1Mo martensites containing nitrogen or carbon

Hardness measurements, dilatometry, internal friction measurements, Mössbauer spectroscopy and transmission electron microscopy are utilized in order to study the effect of tempering on the microstructure of a stainless martensitic steel containing 15% Cr, 1% Mo and 0.6% N. A similar carbon steel containing 15% Cr, 1% Mo and 0.6% C is used for comparison. Tempering of alloy Fe-15Cr-1Mo-0.6N in the low temperature range of 353-473 K leads to formation of hexagonal ?-nitride (Fe,Cr)₂N, which is followed by precipitation of the orthorombic ?-nitride (Fe,Cr)₂N at temperatures of 573-773 K. The hexagonal nitride Cr₂N is precipitated at 923 K and preferably formed at grain boundaries. The alloy Fe-15Cr-1Mo-0.6C shows the expected tempering behaviour. ?-carbide (Fe,Cr)₂C and cementite (Fe,Cr)₃C are precipitated during low temperature ageing, followed by the formation of Cr₇C₃ carbides after the temperature has risen to 873 K. With a similar interstitial content the amount of retained austenite in the nitrogen martensite is nearly twice as high as in the carbon one. Furthermore, the thermal stability of the retained austenite of the nitrogen alloy is substantially higher than that of the carbon steel.     

Influence of tempering temperature on stability of carbide phases in 2.6cr-0.7mo-0.3v steel with various carbon content

The present work evaluates the influence of the bulk carbon content (0.1, 0.006, and 0.005 wt pct) and tempering temperature (823, 853, and 913 K) on stability, chemical composition, and size of carbide particles in 540 ks tempered states of 2.6Cr-0.7Mo-0.3V steel. The scanning transmission electron microscopy/energy-dispersive X-ray spectroscopy (STEM/EDXS) and electron diffraction methods were used to analyze the carbide particles. A characteristic energy-dispersive X-ray (EDX) spectrum can be attributed to each of the identified carbides. The MC carbide is stable in all experimental states. The phase stability of Fe-Cr-rich carbides increased in the order ε, Fe₃C → M₃C → M₇C₃, with tempering temperature increasing. In steels with higher carbon content tempered at low temperature, M₂₃C₆ carbide was also noted. The Mo₂C and M₆C carbides were not observed. It was shown that the decrease of the bulk carbon content has the same influence on the carbide phases stability as the increase of the bulk vanadium content at the unchanged Cr, Mo, C bulk contents and tempering temperature. Similarly, the decrease of tempering temperature has the same influence on the carbide phases stability as the decrease of the bulk Cr content at the unchanged V, Mo, and C bulk contents.     

Effects of alloying additions and austenitizing treatments on secondary hardening and fracture behavior for martensitic steels containing both Mo and W

The effects of alloying additions and austenitizing treatments on secondary hardening and fracture behavior of martensitic steels containing both Mo and W were investigated. The secondary hardening response and properties of these steels are dependent on the composition and distribution of the carbides formed during aging (tempering) of the martensite, as modified by alloying additions and austenitizing treatments. The precipitates responsible for secondary hardening are M₂C carbides formed during the dissolution of the cementite (M₃C). The Mo-W steel showed moderately strong secondary hardening and delayed overaging due to the combined effects of Mo and W. The addition of Cr removed secondary hardening by the stabilization of cementite, which inhibited the formation of M₂C carbides. The elements Co and Ni, particularly in combination, strongly increased secondary hardening. Additions of Ni promoted the dissolution of cementite and provided carbon for the formation of M₂C carbide, while Co increased the nucleation rate of M₂C carbide. Fracture behavior is interpreted in terms of the presence of impurities and coarse cementite at the grain boundaries and the variation in matrix strength associated with the formation of M₂C carbides. For the Mo-W-Cr-Co-Ni steel, the double-austenitizing at the relatively low temperatures of 899 to 816 °C accelerated the aging kinetics because the ratio of Cr/(Mo + W) increased in the matrix due to the presence of undissolved carbides containing considerably larger concentrations of (Mo + W). The undissolved carbides reduced the impact toughness for aging temperatures up to 510 °C, prior to the large decrease in hardness that occurred on aging at higher temperatures.     

Influence of strain-induced martensitic transformations on fatigue crack growth rates in stainless steels

The fatigue crack growth rates (FCGR) of two unstable austenitic stainless steels (Fe-16 Cr-13Ni) and (Fe-18Cr-6.5Ni-0.19C) were determined in theM_s-M_d temperature range where a strain induced μ → α′ martensitic transformation occurs near the crack tip. These FCGR were compared to the rates measured in the stable austenitic phase of a Fe-31.5Ni and a Fe-34 Ni alloy and in the martensitic phase obtained by quenching the Fe-31.5 Ni alloy below M_s. In the Fe-31.5 Ni, the FCGR are an order of magnitude higher in the martensitic than in the austenitic structures for ΔK ≤ 40 ksi in. The FCGR of the stainless steels decrease markedly when the test temperature approachesM _s in theM _s - M_d range. The FCGR for the alloy Fe-18Cr-6.5 Ni-0.19 C in a warm-worked condition are consistently higher than for the same alloy in the annealed condition for ΔK ≤ 40 ksi √in.. The results are discussed in terms of the influence of phase structures, stacking fault energy and work hardening exponent on the FCGR.     

Effect of Silicon on Carbide Precipitation after Tempering of H11 Hot Work Steels

The formation of secondary carbides during tempering of H11 hot work steels at 898 K (625 °C) was studied by transmission electron microscopy (TEM) and related to the previously established effects of Si content on mechanical properties. Lower Si contents (0.05 and 0.3 pct Si) and higher Si contents (1.0 and 2.0 pct Si) were observed to yield different carbide phases and different particle distributions. Cementite particles stabilized by Cr, Mo, and V in the lower Si steels were found to be responsible for similar precipitation hardening effects in comparison to the M₂C alloy carbides in the higher Si steels. The much higher toughness of the lower Si steels was suggested to be due to a finer and more homogeneous distribution of Cr-rich M₇C₃ carbides in the interlath and interpackage regions of the quenched and tempered martensite microstructure. The present effects of Si content on the formation of alloy carbides in H11 hot work steels were found to be the result of the retarding effect of Si on the initial formation of cementite, well known from the early tempering stages in low alloy steels.     

The role of alloy composition in the precipitation behaviour of high speed steels

The role of alloy composition in determining the microstructure and microchemistry of a series of related high speed steels has been investigated by a combination of analytical electron microscopy and atom-probe field ion microscopy. The four steels which were investigated (M2, ASP 23, ASP 30 and ASP 60) cover a large range of C, V and Co contents. Excepting the Co content, the composition of primary MC and M₆C carbides and as-hardened martensite was similar in all four alloys and the major effect of increasing the content of C and V was to increase the volume fraction of MC primary carbides. Precipitation of proeutectoid carbides (mainly MC and M₂C) occurred during hardening of all four steels and the extent of this was greatest in the highly alloyed ASP 60. Tempering at 560°C resulted in the precipitation of extremely fine dispersions of MC and M₂C secondary carbides with very mixed compositions in all four steels. It was found that, as well as hindering the formation of autotempered M₃C in the as-hardened martensite, additions of Co refined the secondary carbide dispersion and delayed overaging reactions. Overaging at 600°C resulted in the precipitation of M₃C, M₆C and M₂₃C₆ at the expense of the fine MC and M₂C secondary carbide dispersion.     

Microstructural characterization of 5 to 9 pct Cr-2 pct W-V-Ta martensitic steels

The microstructure of 9Cr-2W-0.25V-0.1C (9Cr-2WV), 9Cr-2W-0.25V-0.07Ta-0.1C (9Cr-2WVTa), 7Cr-2W-0.25V-0.07Ta-0.1C (7Cr-2WVTa), and 5Cr-2W-0.25V-0.07Ta-0.1C (5Cr-2WVTa) steels (all compositions are in wt pct) have been characterized by analytical electron microscopy (AEM) and atom probe field ion microscopy (APFIM). These alloys have potential applications in fusion reactors because they exhibit reduced neutron activation in comparison to the conventional Cr-Mo steels. The matrix in all four alloys was 100 pct martensite. The precipitate type in the steels depended primarily on the chromium level in the alloy. In the two 9Cr steels, the stable phases were blocky M₂₃C₆ and small spherical precipitates previously identified as MC. The two lower-chromium steels contained blocky M₇C₃ and small needle-shaped carbonitrides in addition to M₂₃C₆. The AEM and APFIM analyses revealed that, in the steels containing tantalum, the majority of the tantalum was in solid solution. With the exception of a few of the small spherical precipitates in low-number densities in the 9Cr-2WVTa, none of the other precipitates contained measurable tantalum. The experimentally observed phases were in agreement with those predicted by phase equilibria calculations using the ThermoCalc software. However, a similar match between the experimental and predicted values of the phase compositions did not occur in some instances. Atom probe analyses directly confirmed the crucial role of trace amounts of nitrogen in the formation of vanadium-rich carbonitrides as predicted by thermodynamic equilibrium calculations.     

Tempering of 2.25 Pct Cr-1 Pct Mo Low Carbon Steels

The effect of carbon level on the tempering behavior at 700°C of 2.25 pct Cr-1 pct Mo steels having typical weld metal compositions has been investigated using analytical electron microscopy and X-ray diffraction techniques. The morphology, crystallography and chemistry, of each of the various types of carbides observed, has been established. It has been shown that each carbide type can be readily identified in terms of the relative heights of the EPMA spectra peaks for iron, chromium, molybdenum, and silicon. A decrease in the carbon level of the steel increases the rate at which the carbide precipitation reactions proceed, and also influences the final product. Of the carbides detected, M₂₃C₆ and M₇C₃ were found to be chromium-based, and their compositions were independent of both the carbon level of the steel and the tempering time. The molybdenum-based carbides, M₂C and M₆C, however, showed an increase in their molybdenum contents as the tempering time was increased. The rate of this increase became greater as the carbon content of the steel was lowered.     

Microstructural evolution of modified 9Cr-1Mo steel

The tempering and subsequent annealing of modified 9Cr-lMo steel have been investigated to determine the influence of trace amounts of V and Nb on the sequence of precipitation processes and to identify the basis for the enhanced high-temperature strength compared to the standard 9Cr-lMo composition. Air cooling (normalizing) from 1045 °C results in the precipitation of fine (Fe, Cr)₃C particles within the martensite laths. Additional carbide precipitation and changes in the dislocation structure occur during the tempering of martensite at 700 °C and 760 °C after normalizing. The precipitation of M₂₃C₆ carbides occurs preferentially at lath interfaces and dislocations. The formation of Cr₂C was detected during the first hour of tempering over the range of 650 °C to 760 °C but was replaced by V₄C₃ within 1 hour at 760 °C. During prolonged annealing at 550 °C to 650 °C, following tempering, the lath morphology remains relatively stable; partitioning of the laths into subgrains and some carbide coarsening are evident after 400 hours of annealing at 650 °C, but the lath morphology persists. The enhanced martensite lath stability is attributed primarily to the V₄C₃ precipitates distributed along the lath interfaces and is suggested as the basis for the improved performance of the modified 9Cr-lMo alloy under elevated temperature tensile and creep conditions.     

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.     

Precipitation Reactions during the Heat Treatment of Ferritic Steels

The precipitation reactions in two ferritic steels, 9Cr-1Mo-V-Nb and 12Cr-1Mo-V-W, were studied. Analytical electron microscopy, optical microscopy, electrolytic extractions, and hardness measurements were used to determine the types, amounts, and effects of precipitates formed as a function of the heat treatment. The effect of variations in the austenitizing treatment was ascertained. In addition to variations in the austenitizing time and temperature, different cooling rates after austenitization were also used. Air cooling after austenitization (normalization) resulted in little precipitation in both alloys. Precipitation in the 12Cr-1Mo-V-W alloy after furnace cooling was found in all cases examined. Under certain conditions precipitation was also found after furnace cooling the 9Cr-1Mo-V-Nb alloy. However, when compared to the amount of precipitate in the fully tempered state, the 9Cr-1Mo-V-Nb showed a much greater variation in the degree of precipitation following furnace cooling. In addition, the matrix microstructure of the 9Cr-1Mo-V-Nb alloy was very sensitive to cooling rate. The precipitation reactions during tempering after a normalizing treatment were followed as a function of tempering treatment. Tempering temperatures were varied from 400 to 780 °C. The carbide precipitation was essentially complete after one hour at 650 °C for both alloys. Analytical microscopy was used to identify the precipitates. In the 9Cr-1Mo-V-Nb alloy, a combination of chromium-rich M₂₃C₆ and vanadium-niobium-rich MC carbides was found. The carbides in the 12Cr-1Mo-V-W alloy were identified as chromium-rich M₂₃C₆ and vanadium-rich MC. The results give an indication of the sensitivity of these alloys to heat treatment variations. This paper is based on a presentation made at the “Peter G. Winchell Symposium on Tempering of Steel” held at the Louisville Meeting of The Metallurgical Society of AIME, October 12-13, 1981, under the sponsorship of the TMS-AIME Ferrous Metallurgy and Heat Treatment Committees.     

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.     

An analytical electron microscopy study of paraequilibrium cementite precipitation in ultra-high-strength steel

To support quantitative design of ultra-high-strength (UHS) secondary-hardening steels, the precipitation of cementite prior to the precipitation of the M₂C phase is investigated using a model alloy. The microstructure of cementite is investigated by transmission electron microscopy (TEM) techniques. Consistent with earlier studies on tempering of Fe-C martensite, lattice imaging of cementite suggests microsyntactic intergrowth of M₅C₂ (Hägg carbide). The concentration of substitutional alloying elements in cementite are quantified by high-resolution analytical electron microscopy (AEM) using extraction replica specimens. Quantification of the substitutional elements in cementite confirms its paraequilibrium (PE) state with ferrite at the very early stage of tempering. The implications of these results are discussed in terms of the thermodynamic driving force for nucleation of the primary-strengthening, coherent M₂C carbide phase. The ferrite-cementite PE condition reduces the carbon concentration in the ferrite matrix with a significant reduction of M₂C driving force. The kinetics of dissolution of PE cementite and its transition to other intermediate states will also influence the kinetics of secondary hardening behavior in UHS steels.     

Carbides in M-50 high speed steel

The carbides in M-50 high speed tool steel were studied in detail. The dissolution of carbides as a function of austenitizing temperature, and their precipitation as a function of tempering temperature were characterized by X-ray diffraction and microchemical analysis. The carbides in the annealed steel are M₂₃C₆, M₆C, M₂C, and MC. Upon austenitizing, with increasing temperatures, the carbides dissolve in the order: M₂₃C₆, metastable M₂C, M₆C, and MC. The residual carbides in the heat treated steel are MC and stable M₂C. The solvus temperatures of M₂₃C₆ and M₆C were determined. Upon tempering the hardened steel, with increasing tempering temperatures, carbides precipitate in the order: M₂₃C₆, metastable M₂C, MC, and M₆C. It is shown that the composition of the precipitated metastable M₂C is different from that of the residual stable M₂C and it varies with the tempering temperature.     

Creep and creep rate curves of a 10cr-30mn austenitic steel during carbide precipitation

The effect of carbide precipitation on creep and creep rate curves was investigated for 10Cr-30Mn austenitic steel containing 0.003 to 0.55 wt pct carbon. After solution annealing, the specimens were subjected to creep testing at 873 K for up to 30 Ms (8300 hours). In the low-carbon steels containing below 0.1 wt pct carbon, where carbide precipitation scarcely occurred, the decrease in creep rate with time in the transient creep region was described by log έ = A - (1/3) log t, where A is a constant depending on stress and carbon concentration. On the other hand, in the high-carbon steels containing above 0.2 wt pct carbon, where extensive precipitation of M₂₃C₆ occurred, the creep rate decreased significantly at long times above 3 to 5 ks (1 hour), deviating from the preceding equation for the low-carbon steels. The Johnson-Mehl equation with the time exponent n = 2/3 provided a reasonable approximation for the significant decrease in creep rate at long times. This resulted from a stress-induced precipitation of M₂₃C₆ on dislocation lines produced by creep deformation. The rate constant of the Johnson-Mehl equation depended on carbon concentration but not on stress levels examined.