Characterization of microstructure and properties of Al–Al<Subscript>3</Subscript>Zr–Al<Subscript>2</Subscript>O<Subscript>3</Subscript> composite

Aluminium-based metal matrix composite strengthened by in situ Al₂O₃ and Al₃Zr particles were synthesized by powder metallurgy route. Phase analysis by X-ray diffraction and scanning electron microscopy revealed that the reaction between Al and ZrO₂ produced Al₂O₃ and Al₃Zr phases in the sintered composites. The hardness of the composite is a strong function of sintering temperature as well as the volume fraction of reinforcements. The dry sliding wear test results clearly indicated that increasing the volume fraction of zirconia particles in the composite improved the wear resistance. Microcutting, ploughing, delamination and oxidation were the main mechanisms of wear.     

Enhanced antibacterial performance of Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>–Ag and MnFe<Subscript>2</Subscript>O<Subscript>4</Subscript>–Ag nanocomposites

In this work, we have described the antibacterial activities of Fe₃O₄ nanoparticles with different organic parts, including Humic acid (HA), Nicotinic acid (Nico) and Histidine (His), and the antibacterial activity of MnFe₂O₄ nanoparticles coated with PANI and SiO₂ against different bacteria and some standard antibacterial drugs. The present study revealed that the newly fabricated various Fe₃O₄ and MnFe₂O₄ nanocomposites, when combined with some different organic parts, are superiour antibacterial agents. Also, the synthesized nanocomposites can be easily separated from aqueous solution by magnetic filtration without any contamination of the medium.     

Growth and properties of Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and SiO<Subscript>2</Subscript> nanolayers on III–V semiconductors

We describe atomic layer deposition of silica and alumina layers on GaAs, InAs, and InSb substrates. The conditions for layer-by-layer growth of surface nanostructures are established, and some of their dielectric parameters are evaluated.     

Thermal and dielectric properties of the LTCC composites based on the eutectic system BaO–Al<Subscript>2</Subscript>O<Subscript>3</Subscript>–SiO<Subscript>2</Subscript>–B<Subscript>2</Subscript>O<Subscript>3</Subscript>

The low-temperature co-fired ceramic (LTCC) composites containing quartz based on the eutectic system BaO–Al₂O₃–SiO₂–B₂O₃ are fabricated at the sintering temperature below 980 °C. Preparation process and sintering mechanism were described and discussed, respectively. The results indicated that the addition of quartz to the eutectic system can availably improve dielectric properties of the LTCC composites. In addition, The LTCC composites with optimum compositions, which were obtained by the regulation of an Al₂O₃ content in the composite, can express excellent dielectric properties (permittivity: 5.94, 5.48; loss: 7 × 10⁻⁴, 5 × 10⁻⁴), considerable CTE values (11.7 ppm. °C⁻¹, 10.6 ppm. °C⁻¹) and good mechanical properties (128 MPa,133 MPa).     

Sintering and microstructure of materials based on the fluorohydroxyapatite–ZrO<Subscript>2</Subscript>–Al<Subscript>2</Subscript>O<Subscript>3</Subscript> system

We have studied the influence of the sintering temperature and modifying additives on the phase composition, microstructure, and mechanical strength of a fluorohydroxyapatite-based composite ceramic material containing 20 wt % zirconia. The addition of 5 wt % alumina has been shown to prevent recrystallization processes and contribute to phase composition stabilization. Moreover, the addition of a sintering aid (2 wt %) has made it possible to lower the sintering temperature to 1200°C and raise the bending strength of the material to 143 MPa.     

Compositional factors affecting the establishment and maintenance of Al<Subscript>2</Subscript>O<Subscript>3</Subscript> scales on Ni–Al–Pt systems

The beneficial role played by platinum addition in promoting the formation of a protective Al₂O₃ scale on representative γ′-Ni₃Al+γ-Ni coating compositions during high-temperature oxidation is discussed. This beneficial effect can be primarily ascribed to the fact that Pt is non-reactive, and its addition decreases the chemical activity of aluminum in γ′. Related to the latter, Pt partitions almost solely to the Ni sites in the ordered L1₂ crystal structure of γ′, which has the effect of amplifying the increase in the Al: Ni atom fraction on a given crystallographic plane containing both Al and Ni. Such an effective Al enrichment at the γ′surface kinetically favors the formation of Al₂O₃ relative to NiO. A further contributing factor is that the Pt-containing γ′-based alloys show subsurface Pt enrichment during the very early stages of oxidation. This enrichment reduces Ni availability and can increase the Al supply to the evolving scale, thus kinetically favoring Al₂O₃ formation. This observed benefit of Pt addition promoting exclusive Al₂O₃-scale growth is inferred to be a special form of the third-element effect.     

Microstructural parameters of dispersion strengthened Cu–Al<Subscript>2</Subscript>O<Subscript>3</Subscript> materials

The aim of the article was to evaluate the microstructural parameters of Cu–Al₂O₃ dispersion strengthened materials with different volume fraction of Al₂O₃ phase. For analyses of dispersoids Al₂O₃, the extraction carbon replica was used. The distribution of Al₂O₃ particles in the matrix was estimated by three methods (quadrant count method, polygonal method, and by interparticle distances), these methods showed that particle distribution in material with 1 vol.% of Al₂O₃ is very close to the Poisson point process (PPP), which is a model of randomly distributed points. Particle distributions in materials with 8 and 10 vol.% of Al₂O₃ achieve features of regularity proved mainly by the spherical contact distance.     

Effect of sintering temperatures on properties of BaO–B<Subscript>2</Subscript>O<Subscript>3</Subscript>–SiO<Subscript>2</Subscript>–Al<Subscript>2</Subscript>O<Subscript>3</Subscript> glass/silica composites for CBGA package

BaO–B₂O₃–SiO₂–Al₂O₃ (BBSA) glass/silica composites synthesized by solid-state reaction method were developed for CBGA packages, and the effects of sintering temperature (900–950 °C) on the phase transformation, microstructure, thermal, mechanical and electrical properties were investigated. XRD results show that the major phases quartz and cristobalite, and the minor phase BaSi₂O₅ are detected in BBSA composites. Furthermore, it was found that the quartz phase transforms to cristobalite phase at 930–940 °C. The formation of cristobalite phase with higher coefficient of thermal expansion (CTE) led to the increase of CTE value of BBSA composites. However, excessive cristobalite phase content would degrade the mechanical properties and the linearity of thermal expansion of the ceramics. BBSA composites sintered at 920 °C exhibited excellent properties: low dielectric constant and loss (ε_r = 6.2, tanδ = 10^?4 at 1 MHz), high bending strength (179 MPa), high CTE (12.19 ppm/°C) as well as superior linearity of the thermal expansion.     

Preparation and properties of antioxidative BaO–B<Subscript>2</Subscript>O<Subscript>3</Subscript>–SiO<Subscript>2</Subscript> glass-coated Cu powder for copper conductive film on LTCC substrate

In this study, uniform BaO–B₂O₃–SiO₂ glass coatings on micro Cu powders with different glass/Cu ratio were prepared by sol–gel method. The pastes prepared with the glass-coated Cu powders were screen printed on low temperature co-fired ceramic (LTCC) substrate. Then the dry films on substrate were binder-burned-out at 400 °C in air and co-fired at 910 °C in N₂ atmosphere. During the binder-burning-out process, the oxidization of the films with 9 and 11 wt% glass was slight because of the improvement of oxidization resistance of the glass-coated Cu powders. Moreover, the sintered film with 9 wt% glass coating showed no crystal phase of copper oxide and had small sheet resistance of 1.3 mΩ/□, which can be used as good conductive thick film on LTCC substrate for microelectronic packaging.     

The crystallographic orientation relationship between Al<Subscript>2</Subscript>O<Subscript>3</Subscript> and MgAl<Subscript>2</Subscript>O<Subscript>4</Subscript> in the composite material Al<Subscript>2</Subscript>O<Subscript>3</Subscript>/Al–Mg–Si alloy

The formation mechanism of spinels on Al₂O₃ particles in the Al₂O₃/Al–1.0 mass% Mg₂Si alloy composite material has been investigated by transmission electron microscopy (TEM) in order to determine the crystallographic orientation relationship. A thin sample of the Al₂O₃/Al–Mg–Si alloy composite material was obtained by the FIB method, and the orientation relationship between Al₂O₃ and MgAl₂O₄, which was formed on the surface of Al₂O₃ particles, was discovered by the TEM technique as follows:

Preparation and characterization of Li<Subscript>2</Subscript>O–CaO–Al<Subscript>2</Subscript>O<Subscript>3</Subscript>–P<Subscript>2</Subscript>O<Subscript>5</Subscript>–SiO<Subscript>2</Subscript> glasses as bioactive material

The aim of the present investigation was to study the role of Al₂O₃ in the Li₂O–CaO–P₂O₅–SiO₂ bioactive glass for improving the bioactivity and other physico-mechanical properties of glass. A comparative study on structural and physico-mechanical properties and bioactivity of glasses were reported. The structural properties of glasses were investigated by X-ray diffraction, Fourier transform infrared spectrometry, scanning electron microscopy and the bioactivity of the glasses was evaluated by in vitro test in simulated body fluid (SBF). Density, compressive strength, Vickers hardness and ultrasonic wave velocity of glass samples were measured to investigate physical and mechanical properties. Results indicated that partial molar replacement of Li₂O by Al₂O₃ resulted in a significant increase in mechanical properties of glasses. In vitro studies of samples in SBF had shown that the pH of the solution increased after immersion of samples during the initial stage and then after reaching maxima it decreased with the increase in the immersion time. In vitro test in SBF indicated that the addition of Al₂O₃ up to 1.5 mol% resulted in an increase in bioactivity where as further addition of Al₂O₃ caused a decrease in bioactivity of the samples. The biocompatibility of these bioactive glass samples was studied using human osteoblast (MG-63) cell lines. The results obtained suggested that Li₂O–CaO–Al₂O₃–P₂O₅–SiO₂-based bioactive glasses containing alumina would be potential materials for biomedical applications.     

The Influence of Corundum Content and Sintering Temperature on the Mechanical Properties of CaO–ZrO<Subscript>2</Subscript>–Al<Subscript>2</Subscript>O<Subscript>3</Subscript> Ceramic Composites

We have studied the mechanical properties (Vickers microhardness H_V and fracture toughness K_C) of nanostructured CaO–ZrO₂–Al₂O₃ ceramic composites as dependent on the content of corundum (0 ≤ \(C_{Al_{2}O_{3}}\) ≤ 25%) and the temperature of sintering (1250°C ≤ T₁ ≤ 1500°C). Optimum value of the corundum content (\(C_{Al_{2}O_{3}}\) = 5%) and optimum regime (T₁ = 1300°C, 5 min; T₂ = 1200°C, 4 h) of two-stage sintering are established, which favor attaining the best mechanical characteristics of ceramic composites (H_V = 12.25 GPa, K_C = 8.47 MPa m^1/2).     

Linear reciprocating wear behaviour of plasma-sprayed Al<Subscript>2</Subscript>O<Subscript>3</Subscript>–Cr<Subscript>2</Subscript>O<Subscript>3</Subscript> coatings at different loading and sliding conditions

Linear reciprocating wear test is carried out on atmospheric plasma-sprayed Al₂O₃–Cr₂O₃ coatings applied on steel substrates. Linear bi-directional sliding wear test of the coatings is performed at different loading and sliding conditions such as load (10, 20 and 30 N), reciprocating amplitude (1.5, 3 and 6 mm) and frequency (5, 10, 15 and 20 Hz) using ball on flat linear reciprocating tribometer. The patterns of tribological behaviour of the coatings, as manifested at the tribo-contact surface, are judged. Results have shown that the wear rate increases with increasing applied load and frequency and that decreases with increasing reciprocating amplitude. Plastic deformation, detachments of unmelted core, reattachments, delamination and adhesive wear dominate the main failure mechanism of coating.     

Fabrication of Yb<Subscript>2</Subscript>O<Subscript>3</Subscript>–Al<Subscript>2</Subscript>O<Subscript>3</Subscript>–P<Subscript>2</Subscript>O<Subscript>5</Subscript>–SiO<Subscript>2</Subscript> Optical Fibers with a Perfect Step-Index Profile by the MCVD Process

An all-vapor phase MCVD process has been proposed for the fabrication of fiber preforms with a Yb₂O₃–Al₂O₃–P₂O₅–SiO₂ multicomponent glass core. We have investigated the tubular preform collapse into a rod and demonstrated approaches capable of preventing P₂O₅ losses in the central part of the core during the collapse process. Preforms with a flat, perfect step-index profile have been fabricated.     

Crystallization and microstructural evolution of MgO–Al<Subscript>2</Subscript>O<Subscript>3</Subscript>–SiO<Subscript>2</Subscript>–TiO<Subscript>2</Subscript>–La<Subscript>2</Subscript>O<Subscript>3</Subscript> glass-ceramics

Crystallization and microstructure of glasses with the molar compositions 1MgO·1.2Al₂O₃·2.8SiO₂·1.2TiO₂·xLa₂O₃ (x = 0.1 and 0.4) were thermally treated at different temperatures in the range from 950 to 1250 °C and then analyzed by X-ray diffraction and scanning electron microscopy, in combination with energy-dispersive X-ray spectroscopy and electron backscatter diffraction. It was found that the microstructure is first homogeneous with the precipitation of randomly distributed crystals and then indialite domains with embedded perrierite and rutile crystals are formed. For higher temperatures or prolonged times, more domains appear and expand into the bulk of the sample. Finally, the entire sample consists of the indialite domains and the boundaries that are enriched in rutile, perrierite, and magnesium aluminotitanate. Nevertheless, very distinct differences are observed between the samples with different La₂O₃ concentrations. For the sample with x = 0.4, the domains were detected at lower temperatures, while the quantity and size of the domains increase faster due to the promoted precipitation of indialite. For the sample with x = 0.1, in addition to the domain boundaries, secondary boundaries between the “regions” (assemblages of the domains) are observed in a larger length scale. The average size of the crystalline phases found between the “regions” is larger than that typically observed at the domain boundaries. The sizes of the crystals at the boundaries decrease with higher concentrations of La₂O₃, and the crystals (especially perrierite) within the domains become larger, resulting in a more homogeneous microstructure. This results in better dielectric properties, i.e., much higher quality factor for the sample with x = 0.4 in comparison to that with x = 0.1 after heat-treatment at 1150 or 1250 °C.     

Compositional dependence of the structural and dielectric properties of Li<Subscript>2</Subscript>O–GeO<Subscript>2</Subscript>–ZnO–Bi<Subscript>2</Subscript>O<Subscript>3</Subscript>–Fe<Subscript>2</Subscript>O<Subscript>3</Subscript> glasses

(10Li₂O–20GeO₂–30ZnO–(40-x)Bi₂O₃–xFe₂O₃ where x = 0.0, 3, 6, and 9 mol%) glasses were prepared. A number of studies, viz. density, differential thermal analysis, FT-IR spectra, DC and AC conductivities, and dielectric properties (constant ε′, loss tan δ, AC conductivity, σ _ac, over a wide range of frequency and temperature) of these glasses were carried out as a function of iron ion concentration. The analysis of the results indicate that, the density and molar volume decrease with an increasing of iron content indicates structural changes of the glass matrix. The glass transition temperature T _g and onset of crystallization temperature T _x increase with the variation of concentration of Fe₂O₃ referred to the growth in the network connectivity in this concentration range, while glass-forming ability parameter ΔT decrease with increase Fe₂O₃ content, indicates an increasing concentration of iron ions that take part in the network-modifying positions. The FT-IR spectra evidenced that the main structural units are BiO₃, BiO₆, ZnO₄, GeO₄, and GeO₆. The structural changes observed by varying the Fe₂O₃ content in these glasses and evidenced by FTIR investigation suggest that the iron ions play a network modifier role in these glasses while Bi₂O₃, GeO₂, and ZnO play the role of network formers. The temperature dependence of DC and AC conductivities at different frequencies was analyzed using Mott’s small polaron hopping model and, the high temperature activation energies have been estimated and discussed. The dielectric constant and dielectric loss increased with increase in temperature and Fe₂O₃ content.     

The effect of Fe contents on the local structure and crystallization behavior of SiO<Subscript>2</Subscript>–CaO–P<Subscript>2</Subscript>O<Subscript>5</Subscript>–Fe<Subscript>2</Subscript>O<Subscript>3</Subscript> glasses

The glass and glass ceramics containing SiO₂–CaO–Fe₂O₃–P₂O₅ were prepared by sol–gel method. The influence of the Fe contents on the crystallization and local structure of the glass and glass ceramics was systematically investigated. The crystal structure of the glass ceramics was identified by XRD characterization. Hematite phase can be precipitated from the glass matrix in all glass ceramics with various Fe contents, and the crystallographic parameters of hematite were determined by XRD Rietveld refinement. The crystallization kinetics of the glasses was investigated in detail. Relative low activation energies were obtained at low Fe contents. The local structure evolution of the glass and glass ceramics has been studied in-depth by means of FTIR and Mössbauer spectroscopy. Fe element is present both as network former and network modifier which significantly influenced the crystallization activation energies of the glasses. The results of this work may be of great significance for the material design and practical applications of bioactive magnetic glass ceramics for hyperthermia.     

Construction of yolk–shell Fe<Subscript>3</Subscript>O<Subscript>4</Subscript>@C nanocubes for highly stable and efficient lithium-ion storage

The yolk-shell Fe₃O₄@C nanocubes were successfully synthesized through carbothermic reduction process from carbon-coated α-Fe₂O₃ precursor. The results show that the yolk-shell Fe₃O₄@C nanocubes are uniformly coated with a thin carbon layer, and a clear cavity about 150 nm in width between Fe3O4 core and carbon shell are formed due to the volume shrinkage during the reduction treatment. The obtained yolk-shell Fe₃O₄@C nanocubes exhibit excellent cycling stability (the discharge capacity is 709.7 mA·h/g after 100 cycles at the current density of 0.1C) and rate performance (1023.4 mA·h/g at 0.1C, 932.5 mA·h/g at 0.2C, 756.1 mA·h/g at 0.5C, 405.6 mA·h/g at 1C, and 332.3 mA·h/g at 2C, and more importantly, when the current density finally backs to 0.1C, a capacity of 776.8 mA·h/g can be restored). The outstanding lithium storage properties may be attributed to the unique yolk-shell structures.     

Improving compressibility and thermal properties of Al–Al<Subscript>2</Subscript>O<Subscript>3</Subscript> nanocomposites using Mg particles

This work presents an efficient technique to improve compressibility and thermal properties of Al–Al₂O₃ nanocomposites. The compressibility behavior was examined by cold compaction test, and the thermal conductivity was calculated through the measured electrical resistivity of the prepared samples. The results showed that the addition of Al₂O₃ to Al matrix improves the compressibility behavior of the produced nanocomposite. However, it has a negative effect on the thermal conductivity of the produced composite. Adding Al₂O₃ hard particles accelerates the fracturing process which improves the compressibility behavior. However, it causes some agglomeration at the grain boundaries which reduce the thermal conductivity. The addition of Mg to Al–Al₂O₃ nanocomposite improves both the compressibility behavior and the thermal conductivity. This is due to the great reduction in the particle size and the agglomeration of reinforcement particles on the grain boundaries which improve the compressibility behavior and the thermal conductivity.     

The mechanism of the failure of the dispersion-strengthened Cu–Al<Subscript>2</Subscript>O<Subscript>3</Subscript> nanosystem

The method of “in situ tensile testing in SEM” is suitable for investigations of fracture mechanisms because it enables to observe and document deformation processes directly, thank to which the initiation and development of plastic deformation and fracture can be reliably described. The deformation and fracture mechanisms of Cu–Al₂O₃ nanomaterials with 5 vol.% of Al₂O₃ phase has been analyzed using technique of the “in situ tensile testing in SEM.” It has been shown that the deformation process causes break-up of large Al₂O₃ particles and decohesion of smaller ones. The final fracture path is influenced also by boundaries of nanograins, through which the principal crack propagates towards the sample exterior surface. Based on the experimental observations, a model of damage and/or fracture mechanisms has been proposed.