The relationship between local non-homogeneous distribution of structural strain and the macroscopic state of loading has already received considerable attention [1, 2]. Knowledge of this relationship promises to contribute to the solution of the problems associated with the initiation and development of yield and the breakdown of material. Three types of strain can be distinguished, taking into account different structural levels: (i) those that are dealt with by the classical theory of elasticity and plasticity, which fit well with the idea of material continuity; (ii) structural strains, which represent strain distribution over structural elements, e.g. grains in polycrystals; and (iii) those that correspond to the local strain field in the neighbourhood of dislocations, vacancies and so on. Deformation inhomogeneity is closely connected with structural strains. These strains characterize the deformed state of each grain. The aim of this work was to prove experimentally the non-homogeneous nature of the plastic strain distribution in polycrystalline atuminium. The correlation between the direction of the principal strains, slip bands and the crystallographic orientation of particular grains was verified by the measured data. Several methods can be used for this purpose. A well-known method is that of Moir6 patterns [3], created by interference of two systems of lines. Artificial marks made on the surface of the specimen are commonly used. We have adopted another method, developed by Berka and Rtlf~ek [4]. This method, called time-based microphotogrammetry, uses elements of the material's structure as natural marks. They can be grain boundaries, natural flaws, etc. The principle of the method consists of a comparison of a stereoscopic pair of micrographs. The first is made in the predeformed state of the material, the second after the well-defined overall deformation. The two micrographs differ slightly. Parallaxes, indirectly expressing displacements, are measured using a stereocomparator. The local displacements in a preselected set of points can then be evaluated quantitatively. The quantitative data obtained can be used for further computations. The measurements were carried out on highpurity aluminium (99.85%) in the form of strip specimens. The grain structure was revealed on their surface in a circular region of diameter 5 mm (Fig. 1)
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