Browsing by Author "Leoni, M"

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    Microstructure and residual stress evolution during cyclic elastoplastic deformation of AISI316L fabricated via laser powder bed fusion
    (Elsevier, 2024-04) Beltrami, M; Pelegatti, M; Magnan, M; Lanzutti, A; Avdeev, M; Luzin, V; Leoni, M; De Bona, F; Salvati, E
    In metal additive manufacturing (MAM), microstructural properties such as texture, residual stresses, and dislocation density have emerged as key factors ruling the resulting mechanical performances. In this study, cylindrical AISI 316L specimens, fabricated with laser powder bed fusion (LPBF), were tested under cyclic elastoplastic (EP) deformation using a constant strain amplitude to highlight the evolution of residual stresses (RS), dislocation density and texture with increasing number of EP cycles, N, across the hardening-softening (H–S) transition stage, in the attempt to find correlations between relevant microstructural parameters and macroscopic properties. The structural and microstructural analysis is carried out through whole powder pattern modeling (WPPM) of neutron diffraction (ND) data and Electron Back-Scattering Diffraction (EBSD) analysis. The H–S transition is found to occur within 7–9 cycles, with RS fading out already after 5 cycles. Across the H–S transition, the trend of the maximum tensile stress correlates closely with the trend of WPPM-calculated total dislocation density, suggesting a major role of dislocations’ characteristics in the evolution of macroscopic mechanical properties. EBSD analysis reveals the rearrangement of geometrically necessary dislocations (GND) into cellular structures, and moderate grain refinement, which are deemed to be responsible for the quick fading of RS in the very early stage of EP loading. ND-based texture analysis reveals a (220) preferential orientation retained throughout the EP tests but with orientation density functions (ODFs) changing non-monotonically with N, suggesting preliminary partial randomization of grains around the deformation axis followed by the recovery of crystallographic anisotropy and more localized ODFs. © 2024 The Authors. Published by Elsevier B.V.
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    Understanding solvothermal crystallization of mesoporous anatase beads by in situ synchrotron PXRD and SAXS
    (American Chemical Society, 2014-07-07) Xia, F; Chen, DH; Scarlett, NVY; Madsen, IC; Lau, D; Leoni, M; Ilavsky, J; Brand, HEA; Caruso, RA
    Submicrometer-sized mesoporous anatase (TiO2) beads have shown high efficiency as electrodes for dye-sensitized solar cells and are recoverable photocatalysts for the degradation of organic pollutants. The detailed mechanism for crystallization of the amorphous TiO2/hexadecylamine (HDA) hybrid beads occurring during the solvothermal process needs to be understood so that reaction parameters can be rationally refined for optimizing the synthesis. In this work, the solvothermal crystallization was monitored by in situ synchrotron powder X-ray diffraction (PXRD) and synchrotron small-angle X-ray scattering (SAXS) techniques. In situ PXRD provided crystallization curves, as well as the time evolution of anatase crystallite mean size and size distribution, and in situ SAXS provided complementary information regarding the evolution of the internal bead structure and the formation of pores during the course of the solvothermal process. By exploring the effects of temperature (140-180 °C), bead diameter (300 and 1150 nm), bead internal structure, and solvent composition (ethanol and ammonia concentrations) on this process, the crystallization was observed to progress 3-dimensionally throughout the entire bead due to solvent entrance after an initial fast partial dissolution of HDA from the nonporous precursor bead. On the basis of the kinetic and size evolution results, a 4-step crystallization process was proposed: (1) an induction period for precursor partial dissolution and anatase nucleation; (2) continued precursor dissolution accompanied by anatase nucleation and crystal growth; (3) continued precursor dissolution accompanied by only anatase crystal growth; and (4) complete crystallization with no significant Ostwald ripening. © 2014 American Chemical Society.