Papers by Author: Cristian Rey

Abstract: The stored energy of two cold rolled IF-Ti steels is calculated using finite element method from an EBSD microstructure. Because the thermo-mechanical treatments are different for the two materials, the parameters of the behaviour law used in the simulation and identified using a polycrystalline model and an inverse method from experimental results are also different. Their variation is due to the number of experimental tests taken into account for their identification and obviously to the thermo-mechanical path. The stored energy is mainly influenced by Lu which represents the mean free path of the mobile dislocations gliding on the system u and which is expressed as a function of a K material parameter. Using one tension test, the experimental stored energy values estimated from neutron diffraction measurements can be reproduced only for a material parameter K fixed.

Abstract: The recrystallization process of two low-carbon ferritic steels with low fraction of alloying elements are modelled. The difference in chemical composition and initial thermomechanical treatment between these two steels can be the cause of the difference in the stored energy distribution after 40% deformation by cold rolling or plane compression simulated by Finite Element Modelling (FEM). In both cases the deformation texture is characterized by the presence of a g- fibre with a reinforcement for the {111}<112> component. The microstructure simulated by FEM is used as initial structure for Monte-Carlo simulations of recrystallization. In these simulations, the variation in chemical composition and initial thermo-mechanical treatment is introduced by the difference in stored energy distribution while recovery, nucleation and grain growth are simulated assuming that grain boundary properties mainly depend on misorientation. Modelling results are in agreement with experimental observations: that is the presence of a g- recrystallization fibre which corresponds to the initial deformed state and the development of {111}<110> component which is not sharp in the deformation microstructure.

Abstract: The feasibility of calcium carbonate-based cements involving the re-crystallization of metastable calcium carbonate varieties has been demonstrated. Two cement compositions were obtained by mixing either calcium carbonate phases (cement A) or a calcium carbonate and a calcium phosphate phase (cement B) with an aqueous media. These cements set and hardened after 30 minutes and 90 minutes respectively. The final composition of cement A was calcite and aragonite whereas cement B lead to a carbonated apatite analogous to bone mineral. Despite poor mechanical properties the presence of a high carbonate content in the final phase might be of interest to increase the cement resorption rate and to favour its replacement by bone tissue. First assays of implantation performed on fresh anatomical pieces (fresh cadavers) at 37°C revealed important advantages of such cement compositions: easiness of use, rapid setting, good adhesion to bone, very good homogeneity and stability of the cement.

Abstract: Nanocrystalline apatites exhibit a very fragile structured hydrated surface layer which is only observed in aqueous media. This surface layer contains mobile ionic species which can be easily exchanged with ions from the surrounding fluids. Although the precise structure of this surface layer is still unknown, it presents very specific spectroscopic characteristics. The structure of the hydrated surface layer depends on the constitutive mineral ions: ion exchanges of HPO4 2- ions by CO3 2- ions or of Ca2+ by Mg2+ ions result in a de-structuration of the hydrated layer and modifies its spectroscopic characteristics. However, the original structure can be retrieved by reverse exchange reaction. These alterations do not seem to affect the apatitic lattice. Stoichiometric apatite also shows HPO4 2- on their surface due to a surface hydrolysis after contact with aqueous solutions. Ion exchange is also observed and the environments of the surface carbonate ions seem analogous to that observed in nanocrystalline apatites. The formation of a hydrated layer in aqueous media appears to be a property common to apatites which has to be taken into account in their reactivity and biological behavior.