Resumo em Inglês:

We have investigated the optical and the structural properties of strained In1-xGaxAsyP1-y/InP and strain compensated In1-xGaxAsyP1-y/In1-zGazAsqP1-q/InP multi-quantum well heterostructures grown by low-pressure metalorganic vapor phase epitaxy at different growth conditions. Our results indicate an increase of the compositional fluctuation of quaternary materials as the alloy composition moves from the outer spinodal isotherm into the miscibility gap region. In1-xGaxAsyP1-y layers grown at high tensile strained values exhibit a three-dimensional-like growth mode. Strain compensated structures revealed the presence of a broad photoluminescence emission band below the fundamental quantum well transition, well defined elongated features along the [011] direction and interface undulations. All these effects were found to be strongly dependent on the growth temperature and the number of wells.

Resumo em Inglês:

Crystallization from solutions was applied to produce stoichiometric and crystalline hydroxyapatite (HAP) suitable for use as a biomaterial. This was accomplished by keeping a low supersaturation through the following procedure: semi-continuous operating mode, slow reactant addition rate and addition of a calcium complexing agent. A high temperature (90 °C) and probably carbonate incorporation also favored the formation of a well crystallized material. A qualitative correlation was found between the supersaturation and HAP properties such as crystallinity and particle size.

Resumo em Inglês:

The effect of the addition of small amounts of doped and undoped poly(o-methoxyaniline) (POMA) on the morphology of melt crystallized PVDF was investigated by means of polarized light optical microscopy. Undoped POMA (POMA-EB) inhibits nucleation and growth of non ringed spherulites, partially formed by the polar <FONT FACE="Symbol">g</font>phase, whereas POMA doped with toluene sulfonic acid (POMA-TSA) favors this process. Moreover, the doping of POMA increases the miscibility between the components of the PVDF/POMA blends, resulting in more homogeneous films. A possible cause of this miscibility increase and for the favoring of the polar <FONT FACE="Symbol">g</font>phase, is the higher polarity of the POMA chains as a result of the doping.

Resumo em Inglês:

The aim of the present work was to produce enhanced-remanence nanocrystalline magnetic material by crystallizing amorphous or partially amorphous Pr4.5Fe77B18.5 alloys by the flash annealing process, also known as the dc-Joule heating process, and to determine the optimal conditions for obtaining good magnetic coupling between the magnetic phases present in this material. Ribbons of Pr4.5Fe77B18.5 were produced by melt spinning and then annealed for 10-30 s at temperatures 500 - 640 °C by passing current through the sample to develop the enhanced-remanence nanocrystalline magnetic material. These materials were studied by X-ray diffraction, differential thermal analysis and magnetic measurements. Coercivity increases of up to 15% were systematically observed in relation to furnace-annealed material. Two different samples were carefully examined: (i) a sample annealed at 600 °C which showed the highest coercive field Hc and remanence ratio Mr/Ms and (ii) a sample annealed at 520 °C which showed phase separation in the second quadrant demagnetization curve. Our results are in agreement with other studies which show that flash annealing improves the magnetic properties of some amorphous ferromagnetic ribbons.

Resumo em Inglês:

This paper presents a methodology for the preparation of <FONT FACE="Symbol">a</font>-HgI2 by Physical Vapor Transport and of PbI2 crystals using the Bridgman technique. The results of the growth of HgI2 diluted in PbI2 by the Bridgman technique are shown for the first time, its limit of solubility having been determined at 600 ppm of HgI2 in the PbI2 matrix. Optical absorption, photoluminescence and electrical conductivity measurements show that the crystals prepared are of good crystalline quality.

Resumo em Inglês:

Mercuric iodide crystals in their platelet habit were grown by the polymer controlled vapor transport method. Mercuric iodide 99% in purity was sublimated at temperatures about 122 - 126 °C and vacuum conditions (10-5 mmHg), after selecting an appropriate polymer. Temperature profiles and experimental heat transfer models were determined for two growth furnaces using different insulator configurations for the cold extreme (air, ceramic wool, grilon, copper and ceramic wool). Growth conditions for few and separate nucleation points and large crystals were determined. Representative samples were characterized by optical microscopy and by measuring the current density and apparent resistivity of the material. Future optimization and comparisons with others mercuric iodide crystal growth methods are included.

Resumo em Inglês:

Visible and Infrared Optical Absorption and Electron Paramagnetic Resonance (EPR) techniques have been used to characterize the intrinsic defects in sillenite type crystals: nominally pure Bi12TiO20 (BTO) and doped with vanadium (BTO:V). Optical quality crystals, with the composition Bi12.04±0.08Ti0.76±0.07V0.16±0.02O20, have been grown. Results obtained by these different techniques have shown unambiguously the 5+ valence state of the vanadium ion in BTO:V crystals. In pure BTO samples, the EPR and optical spectra show strong evidence of the presence of the intrinsic defect BiM3+ + ho+, which consists of a hole h+, mainly located on the oxygen neighbors of the tetrahedrally coordinated Bi3+ ion. After doping with vanadium, results have shown that the characteristic bands, associated to this hole defect center, disappear, suggesting its transformation in single Bi3+. Anisotropy of the EPR spectra , at 20 K, is related to Fe3+ impurities.

Resumo em Inglês:

In this study, the crystallization process of SrTiO3 thin films, prepared by a chemical method, was characterized by Fourier Transformed Infra Red (FT-IR), Grazing Incident X-ray Diffraction (GIXRD), Thermal Analysis (TG) and X-ray Absorption Near Edge Structure (XANES). The results showed that an amorphous inorganic phase is formed, consisting of clusters of oxygen five-coordinate titanium. The amorphous phase begins crystallizing at temperatures above 450 °C. No intermediate crystalline phase and no preferential orientation was observed for films deposited on MgO (100). FT-IR results suggest the presence of the carbonate group. However, the low thermal stability of this group and the low crystallization temperature of the observed SrTiO3 phase indicate that this carbonate is adsorbed.

Resumo em Inglês:

Boron-doped polycrystalline diamond films have been deposited over silicon substrate by hot-filament chemical-vapor-deposition process. A gas mixture of 0,5 vol. % methane and 1 vol. % methanol on hydrogen at a pressure of 50 Torr, have been used. Boric oxide dissolved in methanol have been used as the boron doping source during the diamond growth process. Raman spectroscopy and Scanning Electron Microscopy (SEM) have been performed on the samples. A change of Raman spectra with film doping was observed. The diamond characteristic line at 1333 cm-1 down shifted and its intensity decreased as the film resistivity decreased. On the other hand, a broad peak around 1220 cm-1 appeared and its intensity increased with decreasing film resistivity. No modifications on films morphology have been observed with different boron doping level. The grains were well-faceted with 2 <FONT FACE="Symbol">m</font>m average size

Resumo em Inglês:

Cubic Y zeolite were successfully synthesized using microwave heating for 18 - 25 min, whereas 10 - 50 h are required by hydrothermal heating technique depending upon the lattice Si/Al ratio. To this end, we used a commercial microwave oven modified in order to provide pulsed microwave pumping on the synthesis mixtures. The obtained samples were analyzed by X-ray diffraction, BET surface area and infrared spectroscopy measurements. As a result, we verify that Y zeolite samples obtained from hydrogels containing low aluminum contents, present a good degree of crystallinity and then can be suitable for using in adsorption and catalysis experiments.