Thermodynamic characterization of Al–Cr,Al–Zr,and Al–Cr–Zr alloy systems

Abstract

The equilibrium phase diagrams of Al–Cr, Al–Zr, and Al–Cr-Zr, with particular reference to aluminium-rich alloys, have been critically reviewed. On the basis of these, and consistent with measured thermodynamic values, the binary systems have been thermodynamically characterized. Using these characterizations, phase equilibria have been extrapolated in the ternary, with the intention of augmenting the sparse experimental information concerning the equilibrium liquidus (0–10 at.%Cr, Zr) and solid solution range of aluminium in Al–Cr–Zr. Using the same parameters that define the equilibrium phase relationships, metastable phase relationships can also be extrapolated into the ternary.

MST/418     

Structure,Composition, and Properties of Arc PVD Mo–Si–Al–Ti–Ni–N Coatings

Using an arc physical vapor deposition process, we have produced nanostructured Mo–Si–Al–Ti–Ni–N coatings with a multilayer architecture formed by Mo₂N, AlN–Si₃N₄, and TiN–Ni and a crystallite size on the order of 6–10 nm. We have studied the physicomechanical properties of the coatings and their functional characteristics: wear resistance, adhesion to their substrates, and heat resistance. According to high-temperature (550°C) wear testing and air oxidation (600°C) results, the coatings studied here are wearand heat-resistant under appropriate temperature conditions. Their properties are compared to those of Mo–Si–Al–N coatings.     

Formulation and Comparative Characterization of Chitosan,Gelatin, and Chitosan–Gelatin-Coated Liposomes of CPT-11–HCl

Liposomes containing phosphatidylcholine and cholesterol (uncoated) and coated by chitosan, gelatin, and combination of chitosan and gelatin were prepared by the modified ethanol injection method. The aim of this work was to formulate and characterize liposomes of camptothecin (CPT)-11–HCl (Irinotecan HCl) containing chitosan, gelatin, and both polymers as coating materials; and also to increase its circulation longevity when compared with the free drug while maintaining the agent in its active lactone form. Size, shape, zeta potential, encapsulation efficiency, stability study, in vitro, and in vivo release study were used for characterization of liposomes. The size of liposomes was in the order of uncoated?<?chitosan coated?<?gelatin coated?<?combination of chitosan and gelatin coated. The zeta potential of liposomes was in the order of combination of chitosan and gelatin coated?>?chitosan coated?>?gelatin coated?>?uncoated. The formulations showed the long-term stability. The encapsulation efficiency of liposomes was in order of combination of chitosan and gelatin coated?>?gelatin coated?>?chitosan coated?>?uncoated. The in vitro and in vivo release of drug was observed in the order of combination chitosan and gelatin coated?>?gelatin coated?>?chitosan coated?>?uncoated.     

Fast synthesis,formation mechanism,and control of shell thickness of CuS–polystyrene core–shell microspheres

The silanol-modified polystyrene microspheres were prepared through dispersion polymerization. Then copper sulfide particles were grown on silanol-modified polystyrene through sonochemical deposition in an aqueous bath containing copper acetate and sulfide, released through the hydrolysis of thioacetamide. The resulting particles were continuous and uniform as characterized by scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Fourier transform infrared, thermogravimetric analysis and UV–vis absorption spectroscopy were used to characterize the structure and properties of core–shell particles. The results showed the coating thickness of CuS shell can be controlled by the amount of silanol and the UV–vis absorption intensity of PSt/CuS composite also changed with the coating thickness of CuS.     

Studies of the Hydrolysis of Aluminum Activated by Additions of Ga–In–Sn Eutectic Alloy,Bismuth, or Antimony

Materials Science - We study the Ga–In–Sn eutectic-catalyzed interaction of aluminum alloys with water resulting in the process of hydrolysis and generation of hydrogen. The aluminum...     

Influence of ion energies on the structure,composition, and properties of multilayer Ti–Al–Si–N ion-plasma-deposited coatings

It is established that the energy of deposited particles influences the structure, composition, and properties of multilayer nitride coatings consisting of alternating layers of nanocrystalline TiN and amorphous Si₃N₄ phases with inclusions of nanocrystalline hexagonal AlN formed at energies of titanium, aluminum, and silicon ions exceeding ~317 × 10^–19, 267 × 10^–19, and 230 × 10^–19 J, respectively. As the energy of titanium ions bombarding the substrate increases above ~512 × 10^–19 J, the phase transition from disordered TiN _x to Ti₃N₂ and the appearance of 2- to 3-nm-thick sublayers in 15-nm-thick nanocrystalline TiN _x layers take place in the coating. The maximum hardness of such coatings reaches a level of ~54 GPa.

     

A study of the microstructure, phase composition, and mechanical properties of extruded Mg–9Er–6Y–xZn–0.6Zr magnesium alloys

The microstructure, phase composition, and mechanical properties of Mg–9Er–6Y–xZn–0.6Zr (x = 1, 3, 5 wt%; nominal chemical composition) series alloys were investigated through optical microscopy, X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectrometry, transmission electron microscopy, and tensile tests. Numerous granular Mg₂₄(Er, Y, Zn)₅ phases were distributed in a discontinuous network mainly along the grain boundaries in the alloy with 1 wt% Zn. With increasing Zn content, the Mg₂₄(Er, Y, Zn)₅ phases in the alloys gradually disappeared, the amount of block Mg₁₂Zn(Y, Er) phases increased, and the block size became larger. In addition, a few lamellar phases grew parallel with one another from the grain boundaries to the grain interior in the alloys. The crystallographic structures of the Mg₁₂Zn(Y, Er) and Mg₂₄(Er, Y, Zn)₅ phases were confirmed as 18R-type long-period stacking ordered structures and body-centered cubic structures, respectively. The Mg₁₂Zn(Y, Er) phases with long-period stacking ordered structures increased the strength and toughness of the alloys more than the Mg₂₄(Er, Y, Zn)₅ phases with body-centered cubic structures.     

Measurements of Microstructural, Mechanical, Electrical, and Thermal Properties of an Al–Ni Alloy

The Al–7.5 wt% Ni alloy was directionally solidified upwards with different temperature gradients, $G$ ( $0.86\,\text{ K}~{\cdot }~ \text{ mm}^{-1}$ to $4.24\,\text{ K}~{\cdot }~\text{ mm}^{-1})$ at a constant growth rate, $V$ ( $8.34\,\upmu \text{ m}~{\cdot }~\text{ s}^{-1})$ . The dependence of dendritic microstructures such as the primary dendrite arm spacing ( $\lambda _{1}$ ), the secondary dendrite arm spacing ( $\lambda _{2}$ ), the dendrite tip radius ( $R$ ), and the mushy zone depth ( $d$ ) on the temperature gradient were analyzed. The dendritic microstructures in this study were also compared with current theoretical models, and similar previous experimental results. Measurements of the microhardness (HV) and electrical resistivity ( $\rho $ ) of the directionally solidified samples were carried out. Variations of the electrical resistivity ( $\rho $ ) with temperature ( $T$ ) were also measured by using a standard dc four-point probe technique. And also, the dependence of the microhardness and electrical resistivity on the temperature gradient was analyzed. According to these results, it has been found that the values of HV and $\rho $ increase with increasing values of $G$ . But, the values of HV and $\rho $ decrease with increasing values of dendritic microstructures ( $\lambda _{1}, \lambda _{2}, R,$ and $d$ ). It has been also found that, on increasing the values of temperature, the values of $\rho $ increase. The enthalpy of fusion ( $\Delta {H}$ ) for the Al–7.5 wt%Ni alloy was determined by a differential scanning calorimeter from a heating trace during the transformation from solid to liquid.     

Phase composition,structure, and mechanical properties of arc PVD Mo–Si–Al and Mo–Si–Al–N coatings

Using an arc physical vapor deposition process, we have produced nanostructured Mo–Si–Al coatings with a uniform distribution of equiaxed grains 8–12 nm in size and Mo–Si–Al–N coatings with a multilayer structure and a modulation period from 22 to 25 nm. The former coatings consist of MoSi₂ and Mo and the latter consist of Mo2N and amorphous Si₃N₄ and AlN. The hardness of the Mo–Si–Al–N and Mo–Si–Al coatings is 41 and 18 GPa, respectively; they are similar in resistance to elastic deformation; and the Mo–Si–Al–N coating has a considerably higher resistance to plastic deformation. The coatings have roughly identical coefficients of friction (~0.67–0.69 at 20°C and ~0.52–0.56 at 550°C), but the wear resistance of the Mo–Si–Al–N coating is higher by three and two orders of magnitude at 20 and 550°C, respectively. The coatings of the two systems exhibit good adhesion to the substrate and cohesive fracture. Partial wear of the Mo–Si–Al and Mo–Si–Al–N coatings in the course of scratch testing occurs at indentation loads of 80 and 63 N, respectively.     

Density and thermal expansion of Cr–Fe, Fe–Ni, and Cr–Ni binary liquid alloys

Densities and their temperature coefficients of liquid Cr–Fe, Fe–Ni, and Cr–Ni binary alloys have been measured containerless using the technique of electromagnetic levitation. Data have been obtained in a wide temperature range including the supercooled region. The density measurements indicate that these binary systems have a small and positive excess volume, whereas the excess free energies are negative. The temperature coefficients of these alloys can be estimated from those of the pure components. Hence, possible contributions from the temperature dependence of the excess volume can be ignored to calculate the temperature coefficient of density.     

Influence of fluoride treatment on surface properties,biodegradation and cytocompatibility of Mg–Nd–Zn–Zr alloy

Fluoride treatment is a commonly used technique or pre-treatment to optimize the degradation kinetic and improve the biocompatibility of magnesium-based implant. The influence of changed surface properties and degradation kinetics on subsequent protein adsorption and cytocompatibility is critical to understand the biocompatibility of the implant. In this study, a patent magnesium alloy Mg–Nd–Zn–Zr alloy (JDBM) designed for cardiovascular stent application was treated by immersion in hydrofluoric acid. A 1.5 μm thick MgF₂ layer was prepared. The surface roughness was increased slightly while the surface zeta potential was changed to a much more negative value after the treatment. Static contact angle test was performed, showing an increase in hydrophilicity and surface energy after the treatment. The MgF₂ layer slowed down in vitro degradation rate, but lost the protection effect after 10 days. The treatment enhanced human albumin adsorption while no difference of human fibrinogen adsorption amount was observed. Direct cell adhesion test showed many more live HUVECs retained than bare magnesium alloy. Both treated and untreated JDBM showed no adverse effect on HUVEC viability and spreading morphology. The relationship between changed surface characteristics, degradation rate and protein adsorption, cytocompatibility was also discussed.     

Cold-walled,in-situ sulfurization of Cu–In alloys

This article reports cold-walled, in-situ sulfurization of Cu₁₁In₉ for the formation of CuInS₂. The deposition of the precursor Cu–In layered films, the thermal annealing of the layered films, and the subsequent sulfurization of the annealed films were all performed in chamber without breaking the vacuum. The sulfurization was conducted at various pressures and temperatures under a 10% H₂S/Ar mixture. Conversion of the Cu₁₁In₉ phase to the desired CuInS₂ phase was achieved in 1 h at 146.7 Pa and 550 °C or at 1000 Pa and 450 °C. The CuInS₂ films obtained show low resistivity of the order of 10^? 1 Ω-cm and absorbance > 90%. A CuInS₂ film with a rougher surface exhibits a higher absorption coefficient.     

Effect of polyethylene glycol on the mechanical property, microstructure, thermal stability, and flame resistance of phenol–urea–formaldehyde foams

In this study, polyethylene glycol (PEG) was added to phenol–urea–formaldehyde foam to improve its toughness, and the effects of PEG, with different molecular weights and dosages, on the mechanical property, microstructure, thermal stability, and flame resistance of phenol–urea–formaldehyde foam were studied. The addition of PEG significantly increased the toughness and impact strength and decreased the pulverization rate of the foam. The compression strength of the foam first increased and then decreased with increasing amounts of PEG. When 2 wt% PEGs were added, the compression strength of foams was the highest. The addition of PEG significantly influenced the microstructure of phenol–urea–formaldehyde foams, in which the cell diameter decreased and wall thickness increased with increasing amount and molecular weight of PEG. The addition of PEG also slightly decreased the thermal stability of phenol–urea–formaldehyde foams, and increased the heat release rate, total heat release, and total smoke release of the foams.     

Effects of Ga–Ag, Ga–Al and Al–Ag additions on the wetting characteristics of Sn–9Zn–X–Y lead-free solders

The effects of Ga–Al, Ga–Ag and Al–Ag binary additions on the wetting characteristics of Sn–9Zn–X–Y lead-free solders are studied by the wetting balance method. Experimental results show that Sn–9Zn–1.0Ga–0.3Ag, Sn–9Zn–0.005Al–0.3Ag, and Sn–9Zn–0.3Ga–0.002Al possess better wettability than the other alloys tested. The mechanism by which Ga, Al, and Ag additions improve the wettability is also proposed. It appears that dense aluminum oxide film formation and the enrichment of Ga on the surface may protect the bulk liquid solder from further oxidation. Moreover, results also indicate that, AgZn₃ IMCs layer formed at the interface, which may release reaction energy during the wetting, results in improving the wettability of the solder.     

Characterization of Ge–Bi–S glass by thermal, electrical, switching and optical measurements

A study of the synthesized Ge22.5Bi7S70.5 glassy system has been carried out. Differential thermal analysis data indicate the retention in the as-quenched sample of two amorphous phases. Thermal conductivity, , measurements on bulk sample reveal that the main contribution to is due to phonon thermal conductivity. Thermal evaporation of the synthesized ingot gives films with Ge20.7Bi6.8S72.5 as composition. The values of the activation energy and the pre-exponential factor calculated from the direct current electrical conductivity above 53 °C suggest that carrier conduction occurred between extended states in these films. The I–V characteristics in the off-state and the switching phenomenon are investigated. A memory switch with a threshold voltage decreasing with temperature is detected for the studied films. Optical parameters such as absorption coefficient, optical gap and refractive index are also determined. Comparison with binary Ge–S glass reveals that the addition of Bi introduces additional absorbing states at band edges. © 1998 Kluwer Academic Publishers     

Synthesis,growth mechanism,photoluminescence and field emission properties of metal–semiconductor Zn–ZnO core–shell microcactuses

Metal–semiconductor Zn–ZnO core–shell microcactuses have been synthesized on Si substrate by simple thermal evaporation and condensation route using NH₃ as carrier gas at 600 °C under ambient pressure. Microcactuses with average size of 65–75 μm are composed of hollow microspheres with high density single crystalline ZnO rods. The structure, composition and morphology of the product were characterized by X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDS), scanning electron microscope (SEM), transmission electron microscopy (TEM) and selected area electron diffraction (SAED). A vapor–liquid–solid (VLS) based growth mechanism was proposed for the formation of Zn–ZnO core–shell microcactuses. Room temperature photoluminescence (PL) investigations revealed a strong and broad blue emission band at 441 nm associated with a weak ultraviolet (UV) peak at 374 nm. This blue emission (BE) is different from usually reported green/yellow-green emission from Zn–ZnO or ZnO structures. The field emission (FE) measurements exhibited moderate values of turn-on and threshold fields compared with reported large field emissions for other materials. These studies indicate the promise of Zn–ZnO core–shell microcactuses for the applications in UV-blue light display and field emission microelectronic devices.     

Microstructure,mechanical properties,and cytotoxicity of low Young’s modulus Ti–Nb–Fe–Sn alloys

Journal of Materials Science - Ti–26Nb–2Fe–(0, 2, 4, 6, 8)Sn alloys were prepared by arc melting and subjected to homogenization, cold rolling, and solution treatment. The β...     

Influence of additions of Zr, Ti–B, Sr, and Si as well as of mold temperature on the hot-tearing susceptibility of an experimental Al–2% Cu–1%?Si alloy

This study was undertaken to investigate the effects of chemical composition and mold temperature (MT) on the hot-tearing susceptibility (HTS) of an experimental Al–2% Cu–1% Si alloy using a constrained rod casting mold. The HTS results were then compared with 206 (Al–5 wt% Cu) alloys containing the same additions. In general, the Al–2% Cu–1% Si based alloys exhibited higher resistance to hot-tearing than did the 206-based alloys. It was found that an elevated MT is beneficial in reducing the HTS of the Al–2% Cu–1% Si and 206 alloys in that the HTS value decreased from over 21 to less than 5, as the MT was increased from 250 to 450 °C. Increasing the Si content reduced the HTS of the Al–2% Cu–1% Si alloy considerably; this reduction may be attributed to an increase in the volume fraction of eutectic in the structure. The addition of Sr caused deterioration in the hot-tearing resistance of the base alloy due to the formation of Sr-oxides and an extension of the freezing range of the alloy. The refinement of the grain structure obtained with the Zr–Ti–B addition decreased the severity of hot-tearing as a result of an increase in the number of intergranular liquid films per unit volume and a delay in reaching the coherency point. It was also observed that α-Fe intermetallic particles may impede the propagation of hot-tearing cracks. The Al–2% Cu–1% Si alloy with 1 wt% Si addition was judged to be the best composition in view of its low HTS.