The equiatomic face-centered cubic high-entropy alloy CrMnFeCoNi was severely deformed at room and liquid nitrogen temperature by high-pressure torsion up to shear strains of about 170. Its microstructure was analyzed by X-ray line profile analysis and transmission electron microscopy and its texture by X-ray microdiffraction. Microhardness measurements, after severe plastic deformation, were done at room temperature. It is shown that at a shear strain of about 20, a steady state grain size of 24 nm, and a dislocation density of the order of 1016 m−2 is reached. The dislocations are mainly screw-type with low dipole character. Mechanical twinning at room temperature is replaced by a martensitic phase transformation at 77 K. The texture developed at room temperature is typical for sheared face-centered cubic nanocrystalline metals, but it is extremely weak and becomes almost random after high-pressure torsion at 77 K. The strength of the nanocrystalline material produced by high-pressure torsion at 77 K is lower than that produced at room temperature. The results are discussed in terms of different mechanisms of deformation, including dislocation generation and propagation, twinning, grain boundary sliding, and phase transformation.

No abstract

Ultrafine and nanocrystalline states of equiatomic face‐centered cubic (fcc) high‐entropy alloy (HEA) CoCrFeNiMn (“Cantor” alloy) are achieved by high‐pressure torsion (HPT) at 300 K (room temperature, RT) and 77 K (cryo). Although the hardness after RT‐HPT reaches exceptionally high values, those from cryo‐HPT are distinctly lower, at least when the torsional strain lies beyond γ = 25. The values are stable even during long‐time storage at ambient temperature. A similar paradoxal result is reflected by torque data measured in situ during HPT processing. The reasons for this paradox are attributed to the enhanced hydrostatic pressure, cryogenic temperature, and especially large shear strains achieved by the cryo‐HPT. At these conditions, selected area electron diffraction (SAD) patterns indicate that a partial local phase change from fcc to hexagonal close‐packed (hcp) structure occurs, which results in a highly heterogeneous structure. This heterogeneity is accompanied by both an increase in average grain size and especially a strong decrease in average dislocation density, which is estimated to mainly cause the paradox low strength.

Nanocrystalline materials reveal excellent mechanical properties but the mechanism by which they deform is still debated. X-ray line broadening indicates the presence of large heterogeneous strains even when the average grain size is smaller than 10 nm. Although the primary sources of heterogeneous strains are dislocations, their direct observation in nanocrystalline materials is challenging. In order to identify the source of heterogeneous strains in nanocrystalline materials, we prepared Pd-10 pct Au specimens by inert gas condensation and applied high-pressure torsion (HPT) up to c @ 21. High-resolution transmission electron microscopy (HRTEM) and molecular dynamic (MD) simulations are used to investigate the dislocation structure in the grain interiors and in the grain boundary (GB) regions in the as-prepared and HPT-deformed specimens. Our results show that most of the GBs contain lattice dislocations with high densities. The average dislocation densities determined by HRTEM and MD simulation are in good correlation with the values provided by X-ray line profile analysis. Strain distribution determined by MD simulation is shown to follow the Krivoglaz-Wilkens strain function of dislocations. Experiments, MD simulations, and theoretical analysis all prove that the sources of strain broadening in X-ray diffraction of nanocrystalline materials are lattice dislocations in the GB region. The results are discussed in terms of misfit dislocations emanating in the GB regions reducing elastic strain compatibility. The results provide fundamental new insight for understanding the role of GBs in plastic deformation in both nanograin and coarse grain materials of any grain size.

No abstract

The microstructure and the strength of high pressure torsion processed V-5Cr-5Ti alloy are investigated by X-ray line profile analysis and microhardness testing. High pressure torsion has been applied at 4 and 8 GPa with 0.25, 0.5, 1, 2, 4 and 8 rotations. The X-ray beam of the high angular resolution diffractometer, dedicated for line profile analysis, has a footprint of about 200 m1.5 mm on the specimen. The diffraction patterns have been measured in the center, at half radius and close to the edge of the specimens. This technique has provided a large number of data of the microstructure and hardness as a function of strain up to about 300. The dislocation density determined by X-ray line broadening is correlated and discussed in terms of the strength of the alloy using the Taylor equation.

Martensitic steels are widely used structural materials with outstanding mechanical properties. Their high strength is provided by the non-diffusional phase transformation of fcc γ into thin lamellar bcc plates during fast cooling. Coherency strains between the fcc and bcc lamellae induce large dislocation densities in the range of 1016 m−2, well above the densities attainable by conventional plastic deformation. Using high resolution X-ray line profile analysis, scanning electron microscopy, and hardness tests we show that during tensile deformation when the active Burgers vectors are within the lath plane the lath-packets work soften. On the contrary, when the active Burgers vectors are oblique to the lath-plane the lath-packets work harden. The softening and hardening processes in the differently oriented lath-packets produce a composite of hard and soft components on the length scale of lath-packet size. The stress–strain response of the alloy is discussed in terms of the different mean free paths and the different annihilation lengths of dislocations in the softened and hardened lath-packets. The relatively good ductility is shown to be produced by the composite microstructure induced by plastic strain.

During neutron irradiation of metals, owing to the enhanced number of vacancies and interstitial atoms, the climb motion of dislocations becomes significant at room temperature, leading to a recrystallization of the material. Moreover, the vacancies and interstitial atoms tend to form prismatic dislocation loops that play a crucial role in the plastic properties of the materials. X-ray peak profile analysis is an efficient nondestructive method to determine the properties of dislocation microstructure. In the first half of this article, the foundation of the asymptotic peak broadening theory and the related restricted-moments peak-evaluation method is summarized. After this, the microstructural parameters obtained by X-ray peak profile analysis are reported for irradiated E110 and E110G Zr alloys used as cladding material in the nuclear industry.