Papers by Keyword: Magnesium Titanates

Abstract: The mechanical activation was employed to study the phase evolution of the Mg–TiO2–CaHPO4–CaO nanocrystalline system. The powders mixture with certain weight percent was grinded. Thermal annealing process at 650°C, 900°C and 1100°C temperatures resulted in generation of different compounds like MgTiO3/MgO/Hydroxyapatite (HAp) and MgTiO3/MgO/β-TCP and MgTiO3/Mg2TiO4/MgO/β-TCP, respectively. The compounds were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDX). The consequences of XRD analysis revealed that by increasing temperature, some composites with different morphological and structural features were detected. Beside, due to decomposing of HAp around 800°C, HAp converted to whitlockite (β-TCP) with growth of temperature. According to SEM and TEM observations, it was found that the synthesized powder contained large agglomerates which significant content of finer particles and agglomerates with spherical morphology. Because magnesium titanates based dielectric materials are useful for electrical applications, the electrical property of HAp has been proved, and the incorporation of these materials could result in new nanocrystalline dielectric materials.

Abstract: The following nanocrystalline binary oxide systems were studied: Mg-Ti, Ni-Ti, Zr-Al, as well as some pure and doped unary oxides. The xerogels were heated at a constant T (200 to 1600°C) for 3 to 6 hours. There was a threshold tempearture for oxide formation and in many cases the products were metastable nanocrystalline phases, depending on the grain size and composition, including doping. The oxide phases of Ni-Ti, Mg-Ti, and Zr-Al, formed at 900 °C are different from those formed at higher temperature. New ranges of solid solutions and the formations of higher temperature structures were found. A transition phase can be defined as a structure formed at relative low tempearture, irreversibly transforming at higher temperature into an equilibrium phase of the same elemental composition. Some low temperature transition phases have a structure similar to that of a high temperature equilibrium phase, e.g., (the equilibrium phase is given in parentheses) tetragonal ZrO2 (monoclinic) and low-T qandilite-like solid solutions (qandilite + geikielite). Others are unique with no representation in the equilibrium phase diagram, e.g., gamma-like alumina (corundum) and anatase (rutile), which are formed as nanocrystalline oxides due to a low growth rate caused either by a low temperature of calcination or due to additives. To asses the importance of crystal size in the stabilization of transition phases, the following studies were undertaken: (a) XRPD analysis of all unary, doped and binary compositions; (b) the evolution of transition phases in HT XRPD of the Mg titanates; (c) the phase evolution was studied with time at temperatures were mixtures of transition and equilibrium phases were found; (d) the retention of pure tetragonal ZrO2 on quenching Al-Zr oxides after calcinations at high tempetature; (e) additional evidence from HRTEM, SEM and DTA experiments was also collected. A model, correlating the size effect with the unusual phases and structures is proposed.