A comparison measurement of nonlinear ultrasonic waves in tubes by a microphone and by an optical interferometric probe

This paper deals with the analysis of ultrasonic fields inside waveguides generated by ultrasonic waves of high amplitude. These waves behave nonlinearly, so it is not possible to use standard linear equations to describe their behaviour. Therefore, we started with an experimental determination of the acoustic pressure of air in glass tubes. We chose two methods of measurement--by a microphone and by an optical interferometric probe. The conventional method by a microphone creates numerous problems, which can be avoided by using an optical method, a heterodyne laser interferometer.     

Molecular dynamics of binary metal nitrides and ternary oxynitrides

Ternary systems incorporating metals with oxygen and nitrogen are examined using Tersoff potentials. The apparent success of treating some binary nitride systems using the Tersoff potential is used as a way forward to obtain a new parameter set incorporates atomic features into a series of Tersoff potential for binary nitrides and ternary oxynitrides.     

Photoelectron spectroscopic characterization of titanium-containing amorphous hydrogenated silicon–carbon films (aSi1-xCx:H/Ti)

Titanium-containing amorphous hydrogenated silicon–carbon films (aSi_1-xC_x:H/Ti) have been deposited by reactive magnetron cosputtering. Core-level photoelectron spectroscopy (XPS) and valence-band photoelectron spectroscopy (UPS) have served as means for the characterization of these films. The spectroscopic data are interpreted by a structural model on the basis of a nanocomposite containing clusters of a Ti-C-Si alloy being embedded in an amorphous hydrogenated silicon–carbon matrix (aSi_1-xC_x:H). The Ti-C-Si compound is of metallic character and most likely a substitutional solid solution. This novel nanocomposite material is a promising candidate for applications, especially as optical selective absorber coating for solar collectors. Received: 10 July 2000 / Accepted: 15 September 2000 / Published online: 21 March 2001     

Morphology and electronic structure of nanostructured carbon films embedding transition metal nanoparticles

Inclusions of metals in the growth process of carbon cluster assembled materials (ns-C) induce modifications in the structural and electronic properties of the material. A novel pulsed microplasma cluster source (PMCS) is able to deliver highly intense, collimated and stable beams suitable for producing bulk quantities of cluster-assembled nanocomposite films. Loading of metal nanoparticles into carbon cluster based films is obtained either by mixing a gas phase metallorganic compound with the carrier gas (He) before entering into the source (for example molybdenum (V) isopropoxide), or by using a double component sputtering target (metal (Ti, Ni)/graphite). The study of film morphology on nanometer scale, carried out by transmission electron microscopy (TEM), reveals the dispersion in a ns-C matrix of metallic particles and, in the case of molybdenum containing films, also of carbide particles. Spatially resolved ultraviolet photoemission spectroscopy confirms the segregation of metal particles and exhibits evident anisotropy in the Mo:ns-C films, mainly ascribable to the formation of carbide nanoparticles.     

Negative compressibility

Structures made up from bi‐material elements which can exhibit negative properties, in particular negative compressibility (negative bulk modulus, i.e. expand in size when the external pressure is increased and shrink when the external pressure is decreased) are proposed. This anomalous behaviour is confirmed through finite element modelling. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Electrical and structural properties of Ce0.9CoFe3Sb12 thermoelectric thin films

In this work, we show experimental results for growth conditions of thermoelectric Ce_0.9CoFe₃Sb₁₂ thin films. An rf-magnetron sputtering system has been used to grow the films on single crystal substrates of sapphire (Al₂O₃), silicon (Si), and magnesium oxide (MgO) at different substrate temperatures between 250 and 450 °C. The films were thermoelectrically characterized with resistivity and thermopower measurements as functions of temperature. The results show linear behavior of resistivity with temperature, and thermopower growth with the temperature increase. Such behavior is typical for metallic materials. The structure and surface morphology of the samples were analyzed by X-ray diffraction pattern and atomic force microscopy (AFM), respectively.     

Preparation of Mg55Ni35Si10 Amorphous Powders by Mechanical Alloying and Consolidation by Vacuum Hot Pressing

Amorphous Mg55Ni35Si10 powders are fabricated by using a mechanical alloying technique. The amorphous powders are found to exhibit a relatively high crystallization temperature of 380℃. The as-milled amorphous Mg55Ni35Si10 powders are consolidated successfully into bulk body by vacuum hot pressing technique. Limited nanocrystallization is noticed. The Vickers microhardness range of the Mg55Ni35Si10 bulk sample is 7834 to 8048 MPa. Its bending strength and compressive strength are 529 MPa and 1466 MPa, respectively.     

Synthesis and characterization of a novel magnetic carrier with its composition of Fe3O4/carbon using hydrothermal reaction

In this study, a simple method to prepare a novel magnetic carrier based on carbon matrix has been built by heating the aqueous solution of glucose and oleic acid-stabilized Fe₃O₄ nanoparticle at 170 °C for 3 h. The results show that the surface hydrophobic modification of Fe₃O₄ nanoparticle is necessary for the successful synthesis of Fe₃O₄/C nanocomposition, and a possible formation mechanism of Fe₃O₄/C nanocomposition was presented. The influence of the reaction parameters such as the concentration of oleic acid-stabilized Fe₃O₄ nanoparticle, the reaction time, etc. on the product was also investigated. In the typical reaction (2.5 g/L of oleic acid-stabilized Fe₃O₄ nanoparticle, 0.5 M of glucose), Fe₃O₄/C nanocompositions with the average diameter in the range 100–200 nm were obtained and its saturation is 12.4 emu/g. In order to characterize Fe₃O₄/C nanocompositions, XPS, XRD, FT–IR, and Mössbauer spectra were employed.     

The influence of the dielectric on the properties of dielectromagnetic soft magnetic composites. Investigations with silica and silica hybrid sol–gel derived model dielectric

Dielectromagnetics made from organic–inorganic hybrid silica-coated iron powders were characterised by determination of their physical, mechanical and magnetic properties. The influence of three main factors, dielectric composition, addition level and heat treatment conditions were investigated. Results showed that these factors have significant effects on the performance of the dielectromagnetics. Increase in the organic phase content in these dielectric coatings tends to increase both the electrical resistivity and magnetic permeability of dielectromagnetics, although the strength and density are slightly impaired. Increasing the coating thickness leads to improvements in resistivity and thus reduced eddy current losses, but these are offset by reductions in density, strength and particularly magnetic permeability. A hybrid organic–inorganic coating formulation based on 40 mol% MTMS and 60 mol% TEOS precursors was found to be the optimum composition investigated. Addition levels between 0.1% and 0.3% were found to offer a good compromise between maximum permeability (μ_max>400) and minimum loss (typically <8 W/kg) for operation at 50 Hz/1 T, and the system can be optimised within this range for the desired performance.     

Synthesis and characterization of SiO2-PEG hybrid materials

Sol-gel is a promising technique for the synthesis of organic-inorganic hybrid materials both of class I and II. In materials of class I organic molecules are physically entrapped in an inorganic matrix, while in those of class II organic and inorganic parts are connected by covalent bonds. In this paper a sol-gel procedure to obtain SiO₂-PEG hybrids of class I, in which PEG is simply mixed at the sol stage, is compared to a sol-gel procedure to obtain SiO₂-PEG hybrid materials of class II, where a particular sol-gel Si-C precursor is synthesized. XPS analyses showed the different distribution of the organic phase in the SiO₂ matrix and the bond between PEG and SiO₂ for hybrids of class II. The PEG molecule in hybrid of class II showed an enhanced thermal stability up to 350 °C. Doping with a lithium salt was performed on hybrids of class II, and the ionic conductivity was measured.