The Al–R–Mg (R=Gd, Dy, Ho) systems. Part I: experimental investigation

Key experiments were carried out on the three Al–R–Mg (R=Gd,Dy,Ho) systems and the results obtained used for the thermodynamic optimisation reported in a separate paper in this issue [Caccasmani G, De Negri S, Saccone A, Ferro R. Intermetallics this issue.]. The samples were characterized by differential thermal analysis (DTA), X-ray powder diffraction (XRD), light optical microscopy (LOM), scanning electron microscopy (SEM) and quantitative electron probe microanalysis (EPMA). The isothermal sections at 400 °C are all characterized by extended homogeneity regions at a constant rare earth content. The extension of the (Mg,Al)R solid solution, cP2-CsCl type, varies with the R atomic number. Ternary compounds (τ) of Al₂(R,Mg) stoichiometry (hexagonal Laves phases with MgNi₂-type structure) have been found to exist at 400 °C in all the systems. Their temperatures of formation were detected by DTA measurements.     

On the magnetic and valence properties of Ce---Mg---Y compounds

The structural and magnetic properties of a series of novel compounds in the ternary Ce---Mg---Y system have been studied by X-ray diffraction. SQUID magnetometry and XAS spectroscopy. The crystal structures of the compounds Ce_0.34Y_0.67Mg₂ and Ce_0.49Y_0.51Mg_4.7 have been refined by the Rietveld technique. Magnetic data are consistent with a tripositive ground state ²F_5/2 for the cerium atom. The XAS measurements confirm this result. Crystal field effects are apparent in the magnetic data at temperatures below about 50 K in the compounds with higher Ce concentration.     

Thermodynamic analysis and assessment of the Ce–Ni system

An optimised set of thermodynamic parameters for the Ce–Ni system has been obtained using the CALPHAD approach. A thorough thermodynamic analysis of the system has been carried out using different calorimetric techniques and the data have been used in the assessment. The free energy of the liquid phase has been described as a function of temperature and composition using a Redlich–Kister polynomial. Solid compounds have been considered as stoichiometric with the exception of the Laves phases. The phase diagram and thermodynamic quantities calculated from assessed parameters agree well with experimental data.     

Adsorption of thallium cations on RuO<Subscript>2</Subscript>–TiO<Subscript>2</Subscript> electrodes

The electrochemical ion-exchange properties of RuO₂–TiO₂ film electrodes with different composition have been studied in acidic and alkaline media. Thallium-cation uptake has been observed only from the latter and its extent was found to be a function of electrode potential and composition. At potentials near 0.0 V (RHE), the amount of adsorbed Tl⁺ exhibited a maximum, and decreased with increasing potential, reaching a broad minimum in the range 0.4–0.8 V. A further increase in the electrode potential, above about 1.0 V, led to an increase of adsorbed thallium species, essentially due to deposition of a few layers of Tl(III) hydroxide. In fact, the release of the latter species was found to be much slower than that of thallium ions adsorbed at 0.0 V. For the latter, in turn, the double injection/ejection mechanism, currently accepted to explain the charge-storage in oxide electrodes, seems to be confirmed. The high Γ values attained at 0.0 V indicate that the large ionic radius of Tl⁺ does not prevent its diffusion through the thinner pore texture of the oxide coatings, possibly because of its poor hydration, related with lower charge density at the ion surfaces.     

Analytical Determination of the Distribution of Polishing Time over the Surface of Polished Tiles

Several kinds of glossiness pattern can be seen on the surface of porcelain stoneware tiles right after the polishing process, as a function of the kinematics performed by the polishing heads. For the newest generation of industrial polishing trains, where a transverse oscillation is included, there is still a great need for literature about the resulting patterns. This paper intends to find the spatial distribution of time under polishing analytically using the kinematics equations involved in the polishing process. The measured values of glossiness collected from three polished tiles are also presented. The importance of adopting a good kinematics for the polishing process has been highlighted, and the equations developed herein are useful tools for further attempts at optimizing the polishing process.     

The Bromine Electrode. Part I: Adsorption Phenomena at Polycrystalline Platinum Electrodes

A cyclic voltammetric study of the behaviour of Br^– and Br^– ₃ at Pt electrodes, in the potential range between hydrogen and oxygen evolution, is described. Different experiments were carried out, in the presence of Br^– and Br^– ₃, in which the ratio between the species has been kept constant and equal to 1. The halide concentration was varied between 4 × 10^–6 and 1 × 10^–3 and mol dm^–3, at constant ionic strength, in 1 M HclO₄ as well as in 1 M NaClO₄ adjusted to a pH of 2. Underpotential deposition of Br is observed at potentials as low as –0.125 V vs SCE. The adsorption parameters of Br species were determined from the adsorption/desorption peak pair in the hydrogen adsorption/desorption region, and from the oxide reduction peak data. In the absence of oxygen adsorption, a relatively high coverage of the electrode surface is attained. A Langmuir-type adsorption is observed under the different experimental conditions.     

Optimization of the Kinematics Available in the Polishing Process of Ceramic Tiles by Computational Simulations

This work investigated the influence of the kinematics involved in the polishing process of stoneware tiles over the spatial distribution of abrasive contacts. The basic intention was to delimit the best combinations of both forward and transverse oscillation motions that would result in a uniform polishing effect over the tile surface. Such uniformity was quantitatively represented by the variance of the distribution of polishing time. By means of computational algorithms, a wide range of both forward speed and oscillation frequency were simulated in order to obtain the corresponding distributions of polishing time. The results highlight the importance of adopting good kinematics to avoid excessive polishing gradients. Thus, a large number of kinematic conditions could be potentially recommended, whereas many others were found to be primarily inadequate. In view of this, the simulations carried out herein can be suggested as a useful guide for future phenomenological investigations, and also as a useful tool for polishing industries.     

A Vapor–Liquid–Solid Mechanism for Growing 3C‐SiC Single‐Domain Layers on 6H‐SiC(0001)

Growing device‐quality 3C‐SiC monocrystalline material is still an issue despite two decades of work dedicated to the subject. Using silicon as the substrate generates too many defects in the layers, owing to lattice mismatch, while it is very difficult to control the initial nucleation on an α‐SiC substrate so that 60° rotated domains are randomly formed. Herein, the elaboration of mono‐orientated 3C‐SiC layers on a 6H‐SiC(0001) on‐axis, Si face substrate using a vapor–liquid–solid mechanism is reported. This non‐conventional approach for growing monocrystalline layers involves feeding a Ge–Si melt by a propane flux at a temperature ranging from 1250 to 1550 °C. We show that, by using this technique, the 3C‐SiC material is almost always obtained on an hexagonal substrate, even if the crystal seed is oriented 8° off‐axis. Using on‐axis 6H‐SiC seeds and optimal growth conditions results in the reproducible deposition of single‐domain 3C‐SiC layers. A mechanism is proposed to clarify some aspects of this process.