3.1. Pre-Martensitic State
As was determined, hot deformation via forging of the studied Cu-based alloys permits refining of austenite grains down to 0.5–1 mm [
54,
55]. However, the further subsequent cooling in air entails (i) the decomposition by the scheme β→β
1+γ
2 (at temperatures above the T
ED close to 840 K) and (ii) eutectoid decomposition via β
1→α+γ
2 (at temperatures below T
ED) (
Figure 1a), which is in good correspondence with the known data from [
2,
24,
35,
51,
52,
53,
54,
55,
56,
57,
58,
59,
60,
61,
62,
63,
64,
65]. However, quenching of the alloys after their hot forging allows us to prevent the eutectoid decomposition. At the same time, it is important to take into account that β-austenite at temperatures above T
ED and M
s successfully and successively experiences two transitions (disorder–order), namely, β→β
2(B2)→β
1(D0
3). In this case, as is known, an inheritance of the long-range atomic order from the initial atomically ordered austenitic phase is provided by emerging martensite. The latter fact, as a consequence, determines the thermal elastic behavior of the martensite [
1,
2,
3,
4,
5,
6].
Figure 1b,c displays typical OM images of (b) the grain microstructure of β
1-austenite and (c) the intragrain packet-pyramidal pairwise-twinned morphology of martensite of the quenched alloys (b) Cu–14Al–3Ni and (c) Cu–13.5Al–3.5Ni.
During TEM studies, in the bright- and dark-field images of quenched austenite one can observe the so-called tweed contrast (
Figure 2a,b and
Figure 3a) and anti-phase domain boundaries (APB) (
Figure 2c). Through such examinations, an intricate regular visual image of non-radial diffuse scattering is revealed in selected area electron diffraction (SAED) patterns, and its reconstruction in the form of a reciprocal lattice leads to a successive revealing of the arrangement of the flat diffuse {111}* (walls) that pass through all the nodes hkl, excluding the central node 000 [
6,
66].
The distribution of the intensity of diffuse scattering in these {111}* walls varies heterogeneously and naturally, depending on the position in the reciprocal lattice. A more intense diffuse scattering is observed in the vicinity of any fundamental reflections, rather than in the space between them (
Figure 2 and
Figure 3). According to the diffraction theory, the intensity of diffuse scattering is determined by the relation I ~ |A(k)|
2 (g e
(k))
2, where A(k) is the displacement waver amplitude, k is the wave vector, e
(k) is the polarization vector, and g is the diffraction vector [
6,
66]. The scattering is absent (except for the cases of double diffraction) if the g is directed in parallel to the plane of a diffuse wall (i.e., the vector g lies perpendicular to e
(k) in the given planes passing through the center of the reciprocal lattice). The most intense diffuse streaks in the reciprocal lattice are located parallel to k || <110>*, and e
(k) || <
10>*. A specific feature of the diffuse scattering effects with increasing diffraction angle is the preservation of their sufficiently high intensity in comparison with decreasing intensity of Bragg fundamental reflections. Such scattering occurs at the temperature of observation in situ above M
s by 100–150 K (
Figure 2 and
Figure 3).
As the temperature approaches M
s, the intensity of the diffuse streaks along <112>* and particularly <110>* (according to qualitative and quantitative estimations) increases gradually and, apart from this, which is very important, at these streaks one can see the increase in intensity of the extra reflections (called satellites) at the positions in the space of reciprocal lattice close to 1/2<220>*, 1/3<220>*, 1/6<220>*, 1/2<422>*, and 1/3<422>*. The appearance of such satellites is due to the coexistence of different lattice waves of displacements of k
n atoms in a crystal that is metastable with respect to the shear transition. The diffraction pattern of such a crystal with a single wave of type k
n is described by the vector relation g = g
hkl + Σp
n·k
n, where k
n is the wave vector from the star of the k
n vector, {k
n}, p
n are integers. In this case, it is possible to register paired satellites of the first order (±k). In highly symmetric crystals, multi-ray states are realized, including, for example, two rays of the same set. Therefore, if we denote k
1 = 2/3 2/3 0, k
2 = 2/3 0 2/3, then k
1 + k
2 = 4/3 2/3 2/3. This resulting vector (in units of 2π/a) in the reduced Brullien zone corresponds to the vector k′ = 200−(4/3 2/3 2/3) = 2/3 −2/3 −2/3 and characterizes the diffraction vectors as second order. In other words, satellites of the type 1/3<222>*, 2/3<222>*, and 1/3<422>* that are significantly weaker than the 1/3<220>* satellites of the first order have an interference origin and are second-order satellites. This, in particular, means that the ω-shaped displacements in the D0
3 and L2
1 lattices, the presence of which was assumed in [
66], can be obtained by the interference of waves 1/3 <220>
k<1–10>
e. In addition, it should be noted that the position of the satellites of type 1/2 <422>* coincides with the punctures of the Ewald sphere by diffuse streaks along <110>* (see
Figure 2d and [
66]). Thus, only satellites of the type 1/2<220>*, 1/3<220>*, and 1/6<220>* should be considered the effects of independent diffuse scattering together with continuous diffuse scattering along <110>* (see
Figure 4). The black profile lines represent the experimental profiles of intensity that were measured using the program Digital Micrograph when processing SAED patterns. The red profile lines represent the profiles of intensity calculated by employing a Gauss Function within the framework of the program Origin for fundamental reflections. The blue lines represent the calculated profiles for the satellites of the types 1/6 <220>, 1/3 <220>, and 1/2 <220>. Typical features of (i) the observed diffraction tweed contrast and (ii) diffuse electron scattering, i.e., their periodic “reoccurrence”, regular attenuation, and amplification, make it possible to describe them (namely, i and ii) by certain spectra (see
Figure 5) of the transversal and longitudinal vibration waves in the k-space of reciprocal lattice, which are characterized by the wave (k) and polarization (e
(k)) vectors, and, correspondingly, to identify them with the localized waves of atomic displacements in the space of crystal, which sufficiently periodically distort, on average, the original crystal lattice (
Figure 6). The projections of vectors e
(k), shown in
Figure 5 by streaks or arrows, are characteristic of the waves of enhanced amplitude and, consequently, of intense scattering. The interpretation of the data obtained gives an opportunity to construct a physical model of the real metastable microstructure and its evolution and assess its possible role in the nucleation mechanism of TMT in low-modulus Cu-Al-Ni alloys.
As is known, in the BCC alloys the scattering between reflections in the form of diffuse walls {111}* is stipulated by short-wave acoustic (predominant-in-the-spectrum) vibrations of the non-correlated displacements of closely packed (along <111>) chains of atoms relative to each other. At pre-martensitic softening of elasticity moduli, particularly of C’ [
6,
25,
67], the amplitudes and correlations of such specific linear <111> defects of atomic displacements gradually grow in the close-packed planes {110} (
Figure 6). If the correlations of atomic displacements in these planes are greater than correlations between the planes themselves relative to each other, then the diffuse scattering has the form of solid (continuous) streaks along <110>*. Judging by the character of tweed contrast, such atomic displacements are localized within the volume of nano regions, whose distorted structure and symmetry can be described by the short-range order of atomic displacements (SOD) [
34,
35,
66].
When the alloys are cooled down below a certain temperature T
IncS (at the stage of weakly Incommensurate Satellites), the diffraction pattern commences to be characterized by the appearance of satellites–in the main of the type “1/6”, “1/3” and/or “1/2”, which correspond to long-period modulation (LPM) nanostructures: (for brevity)–LPM-1 (for the satellites of type “1/3”) and LPM-2 (for the satellites of type “1/2”) [
35]. The satellite-related stage can be considered an independent state that replaces SOD domains and is characterized by quasi-stable intermediate LPM shear substructures. Since all crystallographically equivalent variants of the distortion-induced (orientation-related and anti-phase) LPM nanodomains located statistically along the volume of the austenitic phase exist, the structure of such alloys on average retains the original cubic symmetry. According to the diffraction-provided data, the internal distortion and local symmetry of the LPM domains differ from the original one and obviously approach the structure of the future martensitic phases as much as possible while maintaining a coherent connection under the conditions of the specifics of the progressive local instability of the crystal lattice of the austenitic phase and its anharmonism [
6,
35]. In the experiment, this structure-related nucleation mechanism of the TMT is confirmed, firstly, by the fact that the reflections in the SAED patterns from martensite crystals of the β
1′ and γ
1′ phases are located precisely in the positions of the satellites of 1/3 and 1/2 types (see
Figure 3). Secondly, at the nucleation and growth of these phases, there emerge a large number of planar chaotically disposed stacking faults (SF) coplanar to the basal plane of (001) type for both of the martensitic phases β1′ and γ
1′. In this case, one can observe specific characteristic features of the contrast (
Figure 3b,c) and diffuse scattering in the form of distinct narrow continuous streaks passing through Bragg reflections (
Figure 3e,f).
In the modern non-classic crystal-structural description, LPM domains are by themselves special-type nano nuclei (with the structure non-identical to that characteristic of either the austenite phase or would-be martensite phases) and can play the role of real physical centers of nucleation of martensite crystals. Thus, at a certain synchronization between the uniform longitudinal distortion of <100>
k<100>
e Bain type and the transversal static waves of atomic displacements describing the structure of the nano domains LPM-1 by the two waves of 1/6<220>
k<1–10>
e and 1/3<220>
k<1–10>
e type (
Figure 5 and
Figure 6), the structure of the β
1′ martensite of 18R type in the studied alloys can be obtained (see
Figure 6a and
Figure 7a). Additionally, the combination between (i) the uniform longitudinal of <100>
k<100>
e Bain distortion and (ii) the mode of the periodic shuffling displacements of the type 1/2<220>
k <1–10>
e, which form the structure of the nano domains LPM-2, crystallographically presets the trend towards the rearrangement β
1→γ
1’ (
Figure 6b and
Figure 7b). Apparently, in this case, violation of the ideal stacking of atoms along the basal plane (001) is feasible, and this entails the occurrence of various disturbances in the form of stacking faults (
Figure 7).
Interestingly, when measuring the temperature dependences ρ(T) and χ(T) in the thermal cycles (cooling from RT to 90 K–heating to RT), not are only the hysteresis loops of the TMT are determined, but the pre-martensitic deviations of the dependences from linearity of the curves ρ(T) and χ(T) can also be found, despite their being a bit narrower in an interval of the temperatures 20–25 K, which follows from the data of the TEM analysis, obviously being more sensitive (
Figure 8). The temperature dependences for the Cu-14Al-3Ni alloy shown in
Figure 8b demonstrate the TMT hysteresis loops when measured in other thermal cycles cooling–heating (curve 1) or heating–cooling (curve 2). The temperatures determined by the two-tangent method are shown in
Table 2 and are consistent with the XRD phase-composition data (
Figure 9).
As has already been noted, on the one hand, low values of elastic modulus, and on the other hand, the possibility of deformation-induced TMT, both these circumstances determine the unique specific features of the mechanical behavior of metastable alloys. In the next section, we will consider the results of applying SPD to the alloys studied in this work in order to create a nanocrystalline UFG state in them.
3.2. Structure, Phase Composition, and Mechnical Properties of SPD Alloys
According to XRD data, in the course of cooling below the temperature M
s in the studied quenched β
1 Cu-Al-Ni alloys, two martensitic phases indicated as β
1′ (of 18R type) and γ
1′ (of 2H type) are formed (see
Figure 9, curve (a)). It is established that an HPT of 10 revs at RT entails the formation of these alloys of a mixture of the three deformation-induced martensitic phases α′, β
1′, and γ
1′ (
Figure 9, curve (b)) in accordance with [
68]. The Bragg reflections detected in this case are significantly broadened (with a half width up to 2 degrees) and coincide with the most intense diffraction lines from these martensitic phases.
It is important to note that the hysteresis of the TMT (ΔT) in the HPT-treated alloy increases more than three times with a noticeable increase in all critical temperatures. According to the data of XRD analysis of the HPT-treated alloy subjected to annealing at 373 and 473 K, in the alloy, the martensitic phases β
1′ and γ
1′ are preserved and the γ
2–Cu
9Al
4 phase of aging appears (see
Figure 9, curves c, d). An annealing at temperatures higher than A
f, namely, 573–773 K leads to the eutectoid decomposition of β
1 austenite into the phases (α + γ
2) (see
Figure 9, curves e–g). Finally, the annealing at 873 K causes the decomposition of austenite with precipitation of the γ
2 phase (
Figure 9, curve h). Further cooling of the HPT-treated alloy, down to RT, is accompanied by the TMT in the retained β
1 matrix. Therefore, in XRD analysis, β
1-phase reflections, unlike martensitic reflections, are not detected (see
Figure 9).
TEM investigations have shown that as a result of HPT when increasing the number of revolutions from 1 to 10 (and, correspondingly, the degree of deformation) in both alloys, a (progressively) more uniform nano-grained martensitic structure is formed, which is characterized by a ring-wise distribution of Bragg reflections in the SAED patterns (see
Figure 10 and
Figure 11).
According to the data of quantitative analysis of the bright- and dark-field TEM images taken from the alloys after their HPT of 10 revs, the sizes of the observed randomly oriented structural fragments that are most frequently occurring vary within the limits from 10 to 80 nm and are on average 30 nm. It is seen that the larger (in size) of them has plate-like nano twins. Indexing of SAED patterns has shown that the nanocrystalline structure formed in the alloys contains predominantly three martensitic phases (α′ + β1′ + γ1′). The ring distribution of the reflections implies the presence of both small- and large-angle misorientations of the martensitic nanophases that make up the ultrafine-grained (UFG) structure.
We have studied the effect of the temperature of annealing on the microstructure of the HPT-treated alloys using SEM microscopy and revealed the following. Anneals of martensite at 373 and 473 K did not lead to noticeable size-morphological changes in the martensitic UFG structure formed as a result of HPT. However, anneals in the austenite condition (in the temperature range from 573 to 873 K) have provided a noticeable growth of globular grains in the process of formation of UFG states in the HPT-treated alloys (
Figure 12). Employment of the orientational EBSD method has permitted us to establish the specific mechanism of decomposition in the HPT alloys, as a result of which one can observe the formation of a UFG structure of alternating nanophases (see, for example,
Figure 13).
Low-temperature annealing below M
s initiates pro-eutectoid homo- and heterogeneous decomposition of martensite in the HPT-treated alloys with precipitation of an aluminum-enriched γ
2 nano phase (
Figure 14). Namely, the depletion of matrix of aluminum by 1–2 at.% causes the destabilization of austenite and an increase in the critical temperatures of the TMT by 70–150 K (see
Figure 8 and
Table 2).
A study of the alloys in the state of β
1-austenite after HPT of 10 revs and high-temperature anneals was also performed via TEM methods (
Figure 15 and
Figure 16). According to the data of bright-field TEM investigations, it was confirmed that in the UFG β
1 matrix, in the course of annealing, there was a formation and growth of the globular nano crystallites of (in the main) three phases, namely, the β
1, α, and γ
2 phases, judging from the results of indexing of corresponding SAED patterns (the values of the average size <d
G> of the grains–crystallites are given in
Table 3). We have a right to draw a conclusion that annealing at 573 K triggers in the reverted β
1-austenite a combined reaction of the process of recrystallization and eutectoid (α + γ
2) decomposition. In this case, with a background of coarser recrystallized grains, the smaller (comparative) grains–crystallites are still distinguished by the intense deformation-related contrast and they remain virtually unaltered in their sizes. On average, the value of <d
G> is close to 100 nm (see
Figure 15a’). The reflections in the corresponding SAED patterns still exhibited a continuous (solid) ring distribution (
Figure 15a’).
An increase in the annealing temperature to 673 K led to almost complete primary recrystallization of the reverted β
1-austenite and to the formation of a (β
1 + α + γ
2) nano-triplex structure in the composition of a homogeneous UFG austenite at an increased <d
G> value close to 150 nm. The boundaries of grains–crystallites remained rounded and distorted, and the structure still retained an increased number density of defects (
Figure 15b). Intensive enlargement of the α and γ
2-phase globules formed in β
1-austenite at <d
G > close to 350 nm occurred at a higher isochronous annealing temperature of 773 K (
Figure 15c). After annealing at 873 K, the <d
G> for the β
1 and γ
2 phases is already close to 400 nm (
Table 3,
Figure 15d). Imaging of the boundaries of grains–crystallites of a nano-duplex (β
1 + γ
2) structure, which are inherited by martensite, becomes even more distinct, and one can observe a contrast between the twins in martensite. More “sharp” point reflections in the SAED patterns indicate a significant relaxation of the internal stresses and interfacial distortions in the UFG structure formed by the precipitated phases and martensite. The ring-shaped visual character of the less uniform distribution of point reflections in the SAED patterns of HPT-treated alloys after annealing at 673–873 K indicates the preservation of small-angle and large-angle random misorientations of the resulting globular grains–crystallites in the alloy (see
Figure 15a’–d’). Another type of a bimodal single-phase UFG structure, the martensite UFG structure of HPT-treated alloys of the Cu-Al-Ni system, which was formed during short-term thermal action in the course of high-temperature annealing at 1073 K; for 10 s, is shown in
Figure 16. An increase in the annealing time causes accelerated grain growth, since in this case the annealing temperature of 1073 K significantly exceeds T
ED, which is close in this case to 840 K, and this time the increase is inexpedient, as it leads to the softening of the alloy.
Thus, in the result of these TEM investigations it is established that anneals, starting from the temperatures above A
f, lead to recrystallization of the reverted β
1-D0
3 austenite in the HPT-treated alloys Cu–14Al–3Ni and Cu–13.5Al–3.5Ni. In this case, sufficiently homogeneous UFG states can be obtained, the average grain sizes of which increase after annealing at 573–873 K (30 min) in the range from 30 to 400 nm or reach 3.5 μm after short-term annealing at 1073 K, 10 s (
Table 3).
In all cases, the obtained XRD and SAED patterns have shown the presence of γ2-phase reflections, both after low-temperature (below Ms) annealing at 373–473 K, when the HPT-treated alloy has experienced partial decomposition of martensite with the precipitation of disperse (fine) γ2 particles, and after high-temperature annealing as a result of eutectoid (α + γ2) decomposition of austenite at 573–773 K or its (of austenite) pro-eutectoid (β1 + γ2) decomposition at 873 K. If the matrix austenitic β1 phase was preserved after annealing, which is the case for all the selected regimes of treatment, the subsequent cooling to RT was accompanied by TMT.
Data of measurements of Vickers hardness (H
V) at the 1/2 of radius of the specimen disks of the HPT-treated Cu-14Al-3Ni and Cu-13.5Al-3.5Ni alloys in dependence of the quenching and temperature of annealing are listed in
Table 4 and
Table 5 and shown in
Figure 17. It is established that H
V increases after HPT as the temperature of annealing rises, but H
V after double quenching remains slightly lower than after single quenching.
After their annealing at 573–673 K, the HPT-treated Cu-Al-Ni alloys had maximum HV values, up to 6000 MPa after single quenching from 1223 K and 5550 MPa after repeated quenching from 1273 K. The HPT increases HV by 1000 MPa in comparison with HV in the initial quenched austenite condition. The repeated (second) quenching causes the refinement of grain and a better homogenizing of the solid solution of alloys than single quenching; however, as a consequence, this has led to slightly lower values of HV.
The results of measurements of the tensile mechanical properties at RT of the Cu-14Al-3Ni alloy are shown in
Table 6 and
Figure 18. The tests showed that the quenched coarse-grained alloy had an ultimate tensile strength (σ
u) of 620 MPa, a critical stress of martensite shear (σ
M) 160 MPa, and a relative elongation to failure (δ) of 7%. The second quenching of the alloy with some softening due to the creation of a fine-grained state led to an increase in δ up to 11%. In the strengthened UFG alloy, subjected to HPT at RT, the value of δ decreased to 4%, and the destruction was brittle, without the formation of a neck. The plateau of phase fluidity in this case was absent in contrast to the cases of the quenched coarse-grained or the fine-grained alloy (where ε
M = 2%). The rise of the temperature of HPT of n revs to 423 K (by 130 K greater than RT) led to extremely high deformation-induced strengthening of the Cu-14Al-3Ni alloy and to a considerable growth of δ, whose value amounted to 12%. Therefore, in the HPT-treated alloy, the highest mechanical characteristics were achieved in complex. Thus, the yield strength has amounted to 1400 MPa, and the ultimate strength to 1450 MPa at a sufficiently high δ to failure (12%). Considerable changes in the mechanical properties of the alloy were observed after (i) HPT of 10 revs and (ii) isothermal annealing in the temperature range from 573 to 1073 K (see
Table 6). All specimens are characterized by grain size conservation within the UFG structure.
3.3. Fractographic Study
Fractographic investigations of the pattern of failure of the specimens after tensile tests showed that in the initial hot-forged quenched CG alloy the destruction of specimens took place in a brittle manner, predominantly via cleavage along the grain boundaries and large-scale packets of martensite crystals (
Figure 19a). A nano-sized grain–subgrain structure after HPT of 10 revs has revealed the change in the type of fracture and the character of destruction of specimens (
Figure 19b). In the latter case, on the fracture surface, there were many centers of localization of deformation with the formation of small flat dimples and, accordingly, low ridges of separation on the fracture surface. This, as a rule, is typical of the ductile (tenacious), intra-grain mechanism of failure of the alloys with low energy. However, the average size of dimples amounted to 2–5 μm, which was two orders greater than that of the elements of a UFG structure of the HPT-treated alloys. This circumstance testifies to the operation of the special intercrystalline mechanism of the fracture of their destruction, apparently along high-angle boundaries of the UFG structure, since in this case the size of cellular fragments (dimples) of separation during ductile–brittle fracture became two orders of magnitude smaller in comparison with the size of grains and regions of brittle cleavage in the initial coarse-grained alloy. This ultimately determined, in a number of cases, the increased ductility of the UFG alloys preliminarily subjected to HPT and consequent annealing (
Figure 19b–d).
Therefore, it has been established that SPD of the eutectoid Cu-Al-Ni alloys with SMEs is, in certain conditions, an effective method of radical refinement of their grain structure and, as a consequence, attaining the appearance of plasticization. In the present work we have shown that an HPT to the large plastic deformations allows us to attain mechanically induced TMT and the concurrently evolving formation of a homogeneous UFG structure of martensite in metastable austenitic Cu-Al-Ni alloys, which is the case in both studied alloys. The UFG structure is generally characterized by high hardness, strength, as well as by a higher stability of martensitic phases with respect to the case of reverse TMT. The critical temperatures of the TMT of the alloy Cu–14Al–3Ni subjected to HPT of 10 revs have exhibited an increase in value: M
s and M
f by 70 K, and A
s and A
f by 160 K, (see
Table 2). This allowed us to draw a conclusion that the increase in the temperatures of reverse TMT in the cycle of the heating and subsequent cooling when measuring ρ(T) is stipulated in the main, according to the data of phase analysis, by the precipitation effect of the γ
2–Cu
9Al
4 phase (at the boundaries and inside the volume of martensite), which is responsible for both the dimensional and the chemical stabilization of martensitic grains–crystallites, the latter due to their depletion of aluminum and enrichment of copper (by 1–2 at.%, according to the data on M
s and A
f). In this case, a known concentration dependence of the TMT temperatures on the composition in copper and aluminum [
35] gives one the possibility of determining the chemical composition of the β
1 matrix of quenched alloys of the system Cu–Al–Ni.
On the other hand, a number of specific features of the fine structure and phase composition of the alloys after HPT and isothermal annealing were revealed in combined analysis by the XRD, TEM, SEM methods, and measurements of ρ(T). It is established that at lower temperatures of annealing (373–473 K), namely, below Af, in the HPT-treated alloys one can find the preserved martensitic phases. In this case, the appearance of the reflections of the γ2 phase–“phase of ageing”, and the disappearance of the reflections of the strain-induced α’ phase, apparently transforming into β1′ martensite, are recorded. On the contrary, an annealing at higher temperatures, namely, above Af, leads to the disappearance of martensitic phases due to reverse TMT to a UFG austenite. In this case, at annealing below TED the reverted austenitic β1 phase is liable to experience a eutectoid (α + γ2) decomposition into a globular UFG nano-triplex structure, and at annealing above TED the precipitation of the γ2 phase with the formation of a nano-duplex (β1 + γ2) structure is expected. At quenching to RT or upon deformation, the appearance of TMT is possible.
It is important that post-deformation anneals of HPT-treated alloys have entailed the formation of structures capable of exhibiting SME and phase yielding in a wide range of stresses sufficient for the flow of martensite, namely, σ
M from 50 to 450 MPa (
Table 6). Overall, anelastic deformation, including the formation of martensitic crystals, detwinning, and their reorientation in the direction of acting forces, provides an essential contribution to the ability of alloys to deform plastically. Thus, for instance, the alloy Cu–14Al–3Ni after HPT of 10 revs and short-term annealing at a temperature of 1073 K for 10 sec had δ of a relatively moderate value (13%), which was due to the combination of the values of the phase fluidity ε
M and duration of long-term stage of subsequent plastic deformation of martensite (
Table 6). After attainment of the value σ
u = 900 MPa, there was a localization of the deformation with the development of a small reduction in the cross section of the neck.