Papers by Keyword: α-Brass

Abstract: Combined methods to obtain ultra-fine grain (UFG) α-brass samples are proposed. Severe plastic deformation followed by recrystallization was conducted, where multiple rolling and equal channel angular pressing (ECAP) were employed. Recrystallization was accomplished by heat-treatment after the severe plastic deformation, and the grain size after the severe plastic deformation was decreased. By multiple rolling, plates with thickness of 0.1 mm and grain size of 1.0 μm were obtained. By ECAP process, square bar with cross-section of 6 mm × 6 mm and minimum grain size of 4.1 μm was obtained. The 0.2 % proof strength, ultimate tensile strength, and fatigue limit were increased with the value of inverse square root of grain size (Hall-Petch relationship). Then, the 0.2 % proof strength of UFG brass was tenfold, the ultimate tensile strength and the fatigue limit were two fold increases from the conventional α-brass. Because of the high strength, the scatter of fatigue strength of UFG brass was large, which reflects the sensitivity to defects in material.

Abstract: At the entrance temperature of 300°C, the effect of mill temperature on the texture and microstructure evolution was worked to 85/15 α-brass by two rollings with mill temperatures calibrated as 28°C for one rolling and 55°C for another, in which TEM was employed to reveal the microstructures, and ODF to represent the related textures. From the experiment evidence, a detailed discussion was made and led to a conclusion: in current rolling, with recovery, mill temperature influences the rolling texture and microstructure development through chilling and the working temperature induced deformation mechanisms change, the former one affecting B intensities, by contrast, the latter one leading to a texture transition.

Abstract: The evolution of residual stress and crystallographic texture during thermal treatment was studied using X-ray diffraction. Polycrystalline α-brass samples were examined after cold rolling and afterwards after annealing at different temperatures in the range of 50 0C - 450 0C. Additionally, the width of the diffraction peak was measured in order to estimate the variation of the dislocation density. The interpretation of experimental data was based on a fitting procedure for which the anisotropic diffraction elastic constants calculated by a self-consistent approach were used. As the result of analysis, the values of the first order and second order stresses were determined in each sample.