Anisotropy of dielectric losses in Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and SiO<Subscript>2</Subscript> single crystals

The procedure and results of measurements of the dielectric loss tangent using the dielectric resonator technique on azimuthal modes of the HE (quasi-E) and EH (quasi-H) types are considered. The measurements were performed for uniaxial anisotropic single crystals of Al₂O₃ (at a frequency of 11 GHz) and SiO₂ (at 39 GHz) in a temperature range of 80–373 K and for an isotropic single crystal of Y₃Al₅O₂ (YAG) at room temperature in a frequency range of 9–15 GHz. The proposed method revealed the anisotropy of dielectric losses in Al₂O₃ and SiO₂ single crystals in the temperature range studied. According to this, losses along the optical axis of these crystals are lower than in the transverse plane. In the YAG crystal, the Q values for modes of the two types with the same frequency are close, which corresponds to isotropic losses. The dielectric losses in YAG increase in proportion to the frequency.     

Effect of Y<Subscript>2</Subscript>O<Subscript>3</Subscript> on the crystallization behavior of SiO<Subscript>2</Subscript>–MgO–B<Subscript>2</Subscript>O<Subscript>3</Subscript>–Al<Subscript>2</Subscript>O<Subscript>3</Subscript> glasses

A series of glass comprising of SiO₂–MgO–B₂O₃–Y₂O₃–Al₂O₃ in different mole ratio has been synthesized. The crystallization kinetics of these glasses was investigated using various characterization techniques such as differential thermal analysis (DTA), thermo gravimetric analysis (TGA), X-ray diffraction (XRD), and scanning electron microscopy (SEM). Crystallization behavior of these glasses was markedly influenced by the addition of Y₂O₃ instead of Al₂O₃. Addition of Y₂O₃ increases the transition temperature, T _g, crystallization temperature, T _c and stability of the glasses. Also, it suppresses the formation of cordierite phase, which is very prominent and detrimental in MgO-based glasses. The results are discussed on the basis of the structural and chemical role of Y³⁺ and Al³⁺ ions in the present glasses.     

Temperature-Dependent Thermal Boundary Conductance at Al/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and Pt/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> interfaces

With the ever-decreasing size of microelectronic devices, growing applications of superlattices, and development of nanotechnology, thermal resistances of interfaces are becoming increasingly central to thermal management. Although there has been much success in understanding thermal boundary conductance at low temperatures, the current models applied at temperatures more common in device operation are not adequate due to our current limited understanding of phonon transport channels. In this study, the scattering processes in Al and Pt films on Al₂O₃ substrates are examined by transient thermoreflectance testing at high temperatures. At high temperatures, traditional models predict the thermal boundary conductance to be relatively constant in these systems due to assumptions about phonon elastic scattering. Experiments, however, show an increase in the conductance indicating potential inelastic phonon processes.     

Microstructural evolution during direct laser sintering in the Al<Subscript>2</Subscript>O<Subscript>3</Subscript>–SiO<Subscript>2</Subscript> system

The microstructural evolution during direct laser sintering of LSD (Layerwise Slurry Deposition)—samples in the Al₂O₃–SiO₂ system has been investigated. Slurries with a water content of 34 wt.% and a SiO₂/Al₂O₃—ratio of about 3:1 have been used to manufacture layers which—after consecutive drying—have been sintered and laminated by laser treatment. Densified samples can be obtained with laser irradiances from 190 to 270 kW/cm² and scan velocities between 35 and 65 mm/s. Elemental mappings of the layers’ cross sections suggest an inhomogeneous phase distribution in the laser sintered LSD samples with a slight alumina concentration gradient. A lower degree of particle melting in the bottom region of the layers is plausible due to attenuation of the laser beam intensity. SEM and HRTEM micrographs show that after a few seconds of laser treatment relictic starting phase, crystalline alumina plus amorphous silica, occur together with needle like mullite, the latter formed within an amorphous aluminosilicate phase. The resulting phase assemblage reflects the non-equilibrium conditions which can be expected for short time laser treatments. Mullite nucleation within the bulk of the liquid phase rather than in the vicinity of the parent alumina phase suggests that dissolution of alumina is the rate controlling step. Subsequent thermal post treatment in air in a conventional sintering furnace causes an increase of density to about 96% and leads to additional phase reactions. Amorphous silica transforms into cristobalite and the amount of alumina is reduced by additional mullite formation. By both coalescence of individual crystals and grain growth the morphology of the newly formed mullite changes during post heat treatment.     

Ultrasound velocity and absorption in BeO,Al<Subscript>2</Subscript>O<Subscript>3</Subscript>, ZrO<Subscript>2</Subscript>, and SiO<Subscript>2</Subscript> ceramics

We have measured the ultrasound velocity and absorption in BeO, Al₂O₃, ZrO₂, and SiO₂ ceramics. The results indicate that the ultrasound velocity in oxide ceramics depends on the nature of the basic oxide component, the density of the material, and the preferential alignment of the grains. The ultrasound velocity in ceramics is shown to correlate with their thermal conductivity: with increasing thermal conductivity, the ultrasound velocity increases. The ultrasound absorption in oxide ceramics decreases with decreasing temperature, and vice versa, with increasing temperature, the ultrasound attenuation coefficient increases.     

Fabrication of Cr<Subscript>2</Subscript>O<Subscript>3</Subscript>/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> composite nanofibers by electrospinning

PVA(Polyvinyl alcohol)/chromium nitrate/aluminum nitrate composite nanofibers were prepared by using sol–gel processing and electrospinning technique. By high temperature calcinating the above precursor fibers, Cr₂O₃/Al₂O₃ composite nanofibers were successfully obtained. The fibers were characterized by XRD, IR, and SEM, respectively. The results showed that the crystalline phase and the morphology of the fibers depended on the calcination temperatures.     

Antireflecting coating from Ta<Subscript>2</Subscript>O<Subscript>5</Subscript> and SiO<Subscript>2</Subscript> multilayer films

Sol-gel method is important for depositing antireflective coating that allows control over thickness as well as the index of refraction. Antireflective coatings which are produced from Ta₂O₅ and SiO₂ multi-layer thin films using sol-gel spin coating method are presented. The refractive index and the thickness are controlled by the composition and the concentration of the solution respectively. The thickness, refractive index and extinction coefficient of the films were calculated through transmission and reflection measurement by an NKD analyser. Mechanical properties of the films were checked by the cross tape test and dry sun test at 760 W/m². The result shows that the sample heat treated at 450^∘C for 15 min approaches a reflectance with less than 0.5% at around 840 nm.     

Formation and structural phase transitions of mesoporous Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and TiO<Subscript>2</Subscript>/Al<Subscript>2</Subscript>O<Subscript>3</Subscript> xerogels under hydrothermal conditions

We have studied the effect of the hydrothermal synthesis temperature on Al₂O₃ structure formation and examined the role of the phase composition of the precursor gel and surfactant in the formation of the pore structure of Al₂O₃. A technique has been proposed for the synthesis of TiO₂/Al₂O₃ binary xerogels, and the effect of TiO₂ content on the pore structure parameters and adsorption properties of TiO₂/Al₂O₃ has been investigated.     

Microstructure and high-temperature strength of Al<Subscript>2</Subscript>O<Subscript>3</Subscript>/Er<Subscript>3</Subscript>Al<Subscript>5</Subscript>O<Subscript>12</Subscript>/ZrO<Subscript>2</Subscript> ternary melt growth composite

A new Al₂O₃/Er₃Al₅O₁₂(EAG)/ZrO₂ ternary MGC (Melt Growth Composite) with a novel microstructure has been fabricated by unidirectional solidification. This ternary MGC has a microstructure consisting of continuous networks of single-crystal Al₂O₃, single-crystal EAG and fine cubic-ZrO₂ phases without grain boundaries. The ternary MGC has also characteristic dimensions of the microstructure of around 2–4 m for EAG phases, around 2–4 m for Al₂O₃ phases reinforced with around 0.4–0.8 m cubic-ZrO₂ phases. No amorphous phases are formed at interfaces between phases in the ternary MGC. The ternary MGCs flexural strength at 1873 K is approximately 700 MPa, more than twice the 330 MPa of the Al₂O₃/EAG binary MGC. The fracture manner of the Al₂O₃/EAG/ZrO₂ ternary MGC at 1873 K shows the same intergranular fracture as the Al₂O₃/EAG binary MGC, but is significantly different from the transgranular fracture of the sintered ceramic.     

Orientation relationships in multilayer ZnO/In<Subscript>2</Subscript>O<Subscript>3</Subscript> structures

Multilayer ZnO/In₂O₃ structures prepared by annealing Zn _x In₂S_3+x (x = 1, 5) single crystals have been studied by x-ray diffraction and optical microscopy. The results indicate limited texturing of the endotaxial oxide layers. The orientation relationships between the ZnO and In₂O₃ crystallites in neighboring layers are shown to be analogous to those between similar unit cells of single-crystal layers and substrates in epitaxial systems.     

Enhanced thermal stability in K<Subscript>2</Subscript>O-metakaolin-based geopolymer concretes by Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and SiO<Subscript>2</Subscript> fillers addition

Based on the principle of stability of geopolymer gel as refractory binder, a geopolymeric paste in the K₂O–Al₂O₃–SiO₂ system was developed and used to produce refractory concretes by adding various amount of α-quartz sand (grain size in the range 0.1 μm to 1 mm) and fine powder alumina (grain size in the range 0.1–100 μm). The consolidated samples were characterized before and after sintering using optical dilatometer, DSC, XRD and SEM. The total shrinkage in the range of 25–900 °C was less than 3%, reduced with respect to the most diffused potassium or sodium based geopolymer systems, which generally records a >5% shrinkage. The maximum shrinkage of the basic geopolymer composition was recorded at 1000 °C with a 17% shrinkage which is reduced to 12% by alumina addition. The temperature of maximum densification was shifted from 1000 °C to 1150 or 1200 °C by adding 75 wt% α-quartz sand or fine powder alumina respectively. The sequences of sintering of geopolymer concretes could be resumed as dehydration, dehydroxylation, densification and finally plastic deformation due to the importance of liquid phase. The geopolymer formulations developed in this study appeared as promising candidates for high-temperature applications: refractory, fire resistant or insulating materials.     

Role of Ti diffusion on the formation of phases in the Al<Subscript>2</Subscript>O<Subscript>3</Subscript>–Al<Subscript>2</Subscript>O<Subscript>3</Subscript> brazed interface

Diffusivities of Ti, Cu, Al and Ag in the interface of Al₂O₃–Al₂O₃ braze joints using Ag–Cu–Ti active filler alloy, have been calculated by Matano–Boltzman method. The Matano plane has been identified for each elemental diffusion at various brazing temperatures. The diffusivities of Ag, Cu and Al are almost insignificant on formation of interface during brazing, whereas the diffusivity of Ti changes significantly with the brazing temperature and controls the formation of different reaction product in the interface. Presence of TiO and Ti₃Cu₃O phases in the interface has been confirmed by transmission electron microscopy (TEM).     

Low-temperature sintering of SiC reticulated porous ceramics with MgO–Al<Subscript>2</Subscript>O<Subscript>3</Subscript>–SiO<Subscript>2</Subscript> additives as sintering aids

SiC reticulated porous ceramics (SiC RPCs) was fabricated with polymer replicas method by using MgO–Al₂O₃–SiO₂ additives as sintering aids at 1,000∼1,450 °C. The MgO–Al₂O₃–SiO₂ additives were from alumina, kaolin and Talc powders. By employing various experimental techniques, zeta potential, viscosity and rheological measurements, the dispersion of mixed powders (SiC, Al₂O₃, talc and kaolin) in aqueous media using silica sol as a binder was studied. The pH value of the optimum dispersion was found to be around pH 10 for the mixtures. The optimum condition of the slurry suitable for impregnating the polymeric sponge was obtained. At the same time, the influence of the sintering temperature and holding time on the properties of SiC RPCs was investigated. According to the properties of SiC RPCs, the optimal sintering temperature was chosen at 1,300 °C, which was lower than that with Al₂O₃–SiO₂ additives as sintering aids.     

Directional solidification and growth characteristics of Al<Subscript>2</Subscript>O<Subscript>3</Subscript>/Er<Subscript>3</Subscript>Al<Subscript>5</Subscript>O<Subscript>12</Subscript>/ZrO<Subscript>2</Subscript> ternary eutectic ceramic by laser floating zone melting

Directionally solidified Al₂O₃/Er₃Al₅O₁₂/ZrO₂ ternary eutectic ceramic in situ composite rods with length of 110 mm have been fabricated by laser floating zone melting. The microstructural characteristics of steady growth zone, initial growth zone and solid/liquid interface are investigated under high temperature gradient. In the steady growth zone, the eutectic spacing (λ) is rapidly decreased as increasing the growth rate (V), and the corresponding relationship between growth rate and eutectic spacing is determined to be λ = 11.14 × V ^?1/2. The temperature gradient has been measured to be about 5.3 × 10³ K/cm. In the initial growth zone, the melting process and temperature distribution are recorded by infrared thermal imager, and several unstable complex microstructures are observed. In the quenched zone, the regular eutectics with minimum eutectic spacing of 200 nm are obtained. Moreover, the solid/liquid interface during solidification shows convex interface morphology and the interface height is gradually decreased as increasing the growth rate. The eutectic growth behaviors at the center and edge of the as-grown rod are compared and discussed.     

Crystallization and microstructure of a glass seal for rapid laser sealing in the system CaO/Al<Subscript>2</Subscript>O<Subscript>3</Subscript>/SiO<Subscript>2</Subscript>

A glass with the composition 61 CaO·30 Al₂O₃·9 SiO₂ was studied with respect to its crystallization behavior and its suitability as a rapidly crystallizing material for laser sealing. The glass was studied by differential scanning calorimetry; from the profiles recorded, Avrami activation energies and Avrami coefficients were calculated. The latter are in the range between 0.99 and 1.55 which is supposedly attributed to sole surface crystallization. During thermal treatment as well as during laser sealing, Ca₁₂Al₁₄O₃₃, CaAl₂O₄ and Ca₃Al₂O₆ are formed. These phases were also observed in SEM micrographs as evidenced by electron backscatter diffraction from the attributed Kikuchi patterns. Transmission electron microscopy showed a crystallized CaO- and SiO₂-enriched interface which strongly adhered to the Al₂O₃ ceramic. The porosity of the crystallized seal was in the order of few percent. The studied glass proved suitable as crystallizing seal for rapid laser sealing.     

Mechanical properties of bovine hydroxyapatite (BHA) composites doped with SiO<Subscript>2</Subscript>, MgO,Al<Subscript>2</Subscript>O<Subscript>3</Subscript>, and ZrO<Subscript>2</Subscript>

Biologically derived hydroxyapatite from calcinated (at 850 °C) bovine bones (BHA) was doped with 5 wt% and 10 wt% of SiO₂, MgO, Al₂O₃ and ZrO₂ (stabilized with 8% Y₂O₃). The aim was to improve the sintering ability and the mechanical properties (compression strength and hardness) of the resultant BHA-composites. Cylindrical samples were sintered at several temperatures between 1,000 and 1,300 °C for 4 h in air. The experimental results showed that sintering generally occurs at 1,200 °C. The BHA–MgO composites showed the best sintering performance. In the BHA–SiO₂ composites, extended formation of glassy phase occurred at 1,300 °C, resulting in structural degradation of the resultant samples. No sound reinforcement was achieved in the case of doping with Al₂O₃ and zirconia probably due to the big gap between the optimum sintering temperatures of BHA and these two oxides.     

Kinetics of mechanically activated P<Subscript>2</Subscript>O<Subscript>5</Subscript> incorporation into Al<Subscript>2</Subscript>O<Subscript>3</Subscript>

The incorporation of phosphoric anhydride into - and -aluminas during mechanical activation is investigated. An empirical equation is proposed for the kinetics of P₂O₅ incorporation. The effect of the specific power of the mill on the amount of bound P₂O₅ is analyzed.Translated from Neorganicheskie Materialy, Vol. 41, No. 3, 2005, pp. 321–323.Original Russian Text Copyright © 2005 by Kosenko, Smirnova, Denisova.This revised version was published online in April 2005 with a corrected cover date.This revised version was published online in April 2005 with a corrected cover date.     

Hollow biomorphic Al<Subscript>2</Subscript>O<Subscript>3</Subscript> fibers produced from sisal

Al₂O₃ fibers with a hollow morphology were produced by Al-vapor infiltration-reaction and subsequent oxidation from pyrolysed fibers of natural sisal. Following pyrolysis, the bio-fiber template was reacted with gaseous Al at 1,400 °C–1,600 °C in vacuum to form Al₄C₃. After an oxidation/sintering process at 1,550 °C, the biomorphic Al₄C₃ fibers were fully converted into Al₂O₃, maintaining the microstructural features of the native sisal. Phase and microstructural characterization during processing were evaluated by high temperature X-ray diffractometry and scanning electron microscopy, respectively. Thermo-analyses were performed in the Al₄C₃ samples in order to estimate the reactions and the weight change during the oxidation step.