Papers by Author: Tamás Ungár

Abstract: Blends of Cu powders and 3 vol. % carbon nanotubes (CNTs), and an additional sample from pure Cu powder were consolidated by High Pressure Torsion (HPT) at room temperature (RT) and 373 K. The grain size, the lattice defect densities as well as the hardness of the pure and composite materials were determined. Due to the pinning effect of CNTs, the dislocation density is about three times larger, while the grain size is about half of that obtained in the sample consolidated from the pure Cu powder. The increase of the HPT-processing temperature from RT to 373 K resulted in only a slight increase of the grain size in the Cu-CNT composite while the dislocation density and the twin boundary frequency were reduced significantly. The flow stress obtained experimentally agrees well with the value calculated by the Taylor-formula indicating that the strength in both pure Cu and Cu-CNT composites is determined mainly by the interaction between dislocations. The addition of CNTs to Cu yields a significantly better thermal stability of the UFG matrix processed by HPT.

Abstract: X-ray diffraction line profile analysis can be carried out on the hkl planes corresponding to the same texture component or the same crystallographic orientation fiber. It is shown that in textured polycrystalline materials or in thin films or multilayers X-ray line profiles measured on planes corresponding either to the main or the minor texture components can provide the Burgers vector population and dislocations densities in the different texture components separately. The experimental technique is outlined for textured specimens and the multiple convolutional whole profile method, i.e. the CMWP line profile analysis procedure, is presented for its capacity to determine the substructure pertaining to different texture components in textured samples.

Abstract: Uniaxial deformed fcc metal samples have been studied by diffraction peak profile analysis. A method that can explain changes in broadening of different peaks by use of a Taylor model has been investigated. It was found that the method qualitatively describes the changes in broadening in nickel and stainless steel samples. It is argued that the differences between predictions and measurements are a feature of how the different samples deform at the microstructural scale.

Abstract: Nanostructures and microhardness of a commercial purity Al, three binary Al–Mg alloys and a commercial AA5182 alloy subjected to high pressure torsion (HPT) at room temperature were comparatively investigated using high-resolution transmission electron microscopy, X-ray diffraction (XRD) and high-resolution XRD line profile analysis. The hardness values of HPT samples are twice to three times larger than that of the undeformed counterparts. Grain sizes measured by XRD are in the range 10–200 nm with typical average values ranging from 46 to 120 nm. The hardness values and the dislocation densities increased, whereas, the average grain size decreased significantly with increasing Mg contents. Typical dislocation densities are in the range 1.7 × 1014 m-2 – 2.3 × 1015 m-2. However, local densities in grain boundary and triple junction areas might be as high as 1017 m-2. The strengthening mechanisms contributing to high hardness may primarily be attributed to the cooperative interactions of high dislocation densities, grain boundaries and planar interfaces.

Abstract: High resolution X-ray line profile analysis is sensitive to crystallite size, dislocation densities and character, and to planar defects, especially stacking faults or twinning. The different effects of microstructure features can be evaluated separately on the basis of the different corresponding profile functions and the different hkl dependences of line broadening. Profiles of faulted crystals consist of sub-profiles broadened and shifted according to different hkl conditions. The systematic analysis of the breadts and shifts of sub-profiles enables X-ray line profile analysis by using defect related profile functions corresponding to: (i) size, (ii) strain and (iii) planar faults, respectively. It is shown that twinning can either be enhanced or weakened by severe plastic deformation.

Abstract: An Al–0.5 Mg alloy and a commercial AA5182 alloy were subjected to high pressure torsion (HPT) to five turns under pressure of 6 GPa at room temperature. The grain boundary structure and deformation defects were investigated after HPT using high-resolution transmission electron microscopy (HRTEM). Low-angle, high-angle, equilibrium and non-equilibrium grain/subgrain boundaries, twin boundaries, full dislocations, dipoles, microtwins and stacking faults were identified by HRTEM. Extrinsic 60° dislocations in the form of dipoles were frequently observed in non-equilibrium grain/subgrain boundaries. In addition subgrain size distributions and dislocation densities were quantified by x-ray line profile analysis. It was observed that the average grain size decreased from about 120 nm to 55 nm as the Mg content increased from 0.5 to 4.1 wt%. Concomitantly the average stored dislocation density increased from 1.7 to 12.8  1014 m-2. Based on the HRTEM investigations and the x-ray line profile analyses, the deformation mechanism associated with the typical grain boundaries and deformation defects in the aluminium alloys were discussed.

Abstract: The fundamentals of X-ray line profile analysis are summarised in terms of subgrain size and size-distribution, dislocation density and dislocation types, especially edge and screw dislocations, intrinsic and extrinsic stacking faults and twin boundaries and vacancies produced during plastic deformation. It is shown that deformation induced vacancy concentrations in the grain boundaries of compressed copper polycrystals are close to the equilibrium values at the melting temperature. The discrepancy between X-ray and TEM size values is discussed in terms subgrain- and grain size. It is shown that this apparent discrepancy might be used to determine the status of fragmentation by severe plastic deformation.

Abstract: The effect of the nominal Mg content and the milling time on the microstructure of mechanically alloyed Al(Mg) solid solutions is studied. The crystallite size distribution and the dislocation structure are determined by X-ray diffraction peak profile analysis. Magnesium gradually goes into solid solution during ball milling and after 3 h almost all of the Mg atoms are soluted into the Al matrix. With increasing milling time the Mg content in solid solution, the dislocation density as well as the hardness are increasing, whereas the crystallite size is decreasing. A similar tendency of these parameters is observed at a particular duration of ball milling with increasing of the nominal Mg content. At the same time for a long milling period the dislocation density slightly decreases together with a slight reduction of the hardness.

Abstract: Anisotropic strain broadening of diffraction peaks can be parameterised by dislocation contrast factors. A comprehensive software has been developed and made available through the internet to determine the individual and averaged contrast factors which are also compiled for cubic and hexagonal crystals. Using the theoretical and the measured values of contrast factor the microstructure of the specimen can be characterised in terms of active slip systems, Burgers vector populations, dislocation densities and crystallite size- and size distribution.