Laser-Deposited In Situ TiC-Reinforced Nickel Matrix Composites: 3D Microstructure and Tribological Properties

A new class of Ni-Ti-C-based metal-matrix composites has been developed using the laser-engineered net shaping? process. These composites consist of an in situ formed and homogeneously distributed titanium carbide (TiC) phase reinforcing the nickel matrix. Additionally, by tailoring the Ti/C ratio in these composites, an additional graphitic phase can also be engineered into the microstructure. Serial-sectioning, followed by three-dimensional reconstruction of the microstructure in these composites, reveals homogeneously distributed primary and eutectic titanium carbide precipitates as well as a graphitic phase encompassing the primary carbides within the nickel matrix. The morphology and spatial distribution of these phases in three dimensions reveals that the eutectic carbides form a network linked by primary carbides or graphitic nodules at the nodes, which suggests interesting insights into the sequence of phase evolution. These three-phase Ni-TiC-C composites exhibit excellent tribological properties, in terms of an extremely low coefficient of friction while maintaining a relatively high hardness.     

Biocompatible composites of fibrous nanohydroxyapatite embedded in a polydimethylsiloxane

Silicone elastomers have the potential to be a valuable biomaterial due to their mechanical and chemical properties, easy processing, and high gas permeability. Some inherent properties of the pure silicone implant such as high hydrophobicity and low load bearing capacity can be problematic for biomedical applications. The issues were addressed by fabricating hydroxyapatite nanofiber/polydimethylsiloxane nanocomposites. The morphology of nanocomposite structures was visualized by high resolution transmission electron microscopy and field emission scanning electron microscopy. Improved mechanical strength and compliance of the prepared nanocomposite structures were obtained by frequency sweep and creep measurements. Surface hydrophilicity of polydimethylsiloxane was enhanced by hydroxyapatite nanofiber incorporation into the polymer matrix. The cytotoxicity and biocompatibility of the structures were analyzed using breast epithelial cells (MDA MB 231 cell line). These studies showed that the nanocomposite scaffold did not leach any cytotoxic material and showed better cell adhesion and cell proliferation compared to the unfilled elastomer.     

Perforation resistance of five different high-strength steel plates subjected to small-arms projectiles

Thin plates of high-strength steel are frequently being used both in civil and military ballistic protection systems. The choice of alloy is then a function of application, ballistic performance, weight and price. In this study the perforation resistance of five different high-strength steels has been determined and compared against each other. The considered alloys are Weldox 500E, Weldox 700E, Hardox 400, Domex Protect 500 and Armox 560T. The yield stress for Armox 560T is about three times the yield stress for Weldox 500E, while the opposite yields for the ductility. To certify the perforation resistance of the various targets, two different ballistic protection classes according to the European norm EN1063 have been considered. These are BR6 (7.62 mm Ball ammunition) and BR7 (7.62 mm AP ammunition), where the impact velocity of the bullet is about 830 m/s in both. Perforation tests have been carried out using adjusted ammunition to determine the ballistic limit of the various steels. In the tests, a target thickness of 6 mm and 6 + 6 = 12 mm was used for protection class BR6 and BR7, respectively. A material test programme was conducted for all steels to calibrate a modified Johnson–Cook constitutive relation and the Cockcroft–Latham fracture criterion, while material data for the bullets mainly were taken from the literature. Finally, results from 2D non-linear FE simulations with detailed models of the bullets are presented and the different findings are compared against each other. As will be shown, good agreement between the FE simulations and experimental data for the AP bullets is in general obtained, while it was difficult to get reliable FE results using the Lagrangian formulation of LS-DYNA for the soft core Ball bullet.     

Simplified Impedance Model for Adhesively Bonded Piezo-Impedance Transducers

The electromechanical impedance technique employs surface-bonded lead zirconate titanate piezoelectric ceramic patches as impedance transducers for structural health monitoring and nondestructive evaluation. The patches are bonded to the monitored structures using finitely thick adhesive bond layer, which introduces shear lag effect, thus invariably influencing the electromechanical admittance signatures. This paper presents a new simplified impedance model to incorporate shear lag effect into electromechanical admittance formulations, both one-dimensional and two-dimensional. This provides a closed-form analytical solution of the inverse problem, i.e. to derive the true structural impedance from the measured conductance and susceptance signatures, thus an improvement over the existing models. The influence of various parameters (associated with the bond layer) on admittance signatures is investigated using the proposed model and the results compared with existing models. The results show that the new model, which is far simpler than the existing models, models the shear lag phenomenon reasonably well besides providing direct solution of a complex inverse problem.     

New observations in micro-pop-in issues in nanoindentation of coarse grain alumina

The present experiments were focused on nanoindentation behaviour and the attendant “micro-pop-in” in a dense (～95% of theoretical) coarse-grain (～20 μm) alumina ceramic as a function of loading rate variations at three constant peak loads in the range of 10⁵–10⁶ μN. Based on the experimental results here we report for the first time, to the best of our knowledge, an increase in intrinsic nano scale contact resistance as well as the nanohardness with the loading rate. These observations were explained in terms of the correlation between the nanoscale plasticity and shear stress active just underneath the nanoindenter.     

Thermal,Structural, and Enhanced Photoluminescence Properties of Eu3+‐doped Transparent Willemite Glass–Ceramic Nanocomposites

The precursor glass in the ZnO–Al₂O₃–B₂O₃–SiO₂ (ZABS) system doped with Eu₂O₃ was prepared by the melt‐quench technique. The transparent willemite, Zn₂SiO₄ (ZS) glass–ceramic nanocomposites were derived from this precursor glass by a controlled crystallization process. The formation of willemite crystal phase, size, and morphology with increase in heat‐treatment time was examined by X‐ray diffraction (XRD) and field‐emission scanning electron microscopy (FESEM) techniques. The average calculated crystallite size obtained from XRD is found to be in the range 18–70 nm whereas the grain size observed in FESEM is 50–250 nm. The refractive index value is decreased with increase in heat‐treatment time which is caused by the partial replacement of ZnO₄ units of ZS nanocrystals by AlO₄ units due to generation of vacancies. Fourier transform infrared (FTIR) reflection spectroscopy was used to evaluate its structural evolution. Vickers hardness study indicates marked improvement of hardness in the resultant glass‐ceramics compared with its precursor glass. The photoluminescence spectra of Eu³⁺ ions exhibit emission transitions of ⁵D₀→⁷F_j (j = 0, 1, 2, 3, and 4) and its excitation spectra show an intense absorption band at 395 nm. These spectra reveal that the luminescence performance of the glass–ceramic nanocomposites is enhanced up to 17‐fold with the process of heat treatment. This enhancement is caused by partitioning of Eu³⁺ ions into glassy phase instead of into the willemite crystals with progress of heat treatment. Such luminescent glass–ceramic nanocomposites are expected to find potential applications in solid‐state red lasers, phosphors, and optical display systems.     

A relativistic two-parameter core-envelope model of compact stars

A core-envelope model for a spherical superdense distribution of matter is reported, with a core consisting of anisotropic fluid engulfed by an envelope containing fluid with isotropic pressure is reported. The background space-time of the whole configuration is characterized by a two-parameter parabolic geometry. The physical plausibility of the model is examined both analytically and numerically, and suitability of the model for describing space-times of superdense stars containing strange matter, such as Her-X1 and SAX, is also discussed.     

Development and long-term in vivo evaluation of a biodegradable urethane-doped polyester elastomer

We have recently reported upon the development of crosslinked urethane-doped polyester (CUPE) network elastomers, which was motivated by the desire to overcome the drawbacks presented by crosslinked network polyesters and biodegradable polyurethanes for soft tissue engineering applications. Although the effect of the isocyanate content and post-polymerization conditions on the material structure-property relationship was examined in detail, the ability of the diol component to modulate the material properties was only studied briefly. Herein, we present a detailed report on the development of CUPE polymers synthesized using diols 4, 6, 8, 10, or 12 methylene units in length in order to investigate what role the diol component plays on the resulting material's physical properties, and assess their long-term biological performance in vivo. An increase in the diol length was shown to affect the physical properties of the CUPE polymers primarily through lowered polymeric crosslinking densities and elevated material hydrophobicity. The use of longer chain diols resulted in CUPE polymers with increased molecular weights resulting in higher tensile strength and elasticity, while also increasing the material hydrophobicity to lower bulk swelling and prolong the polymer degradation rates. Although the number of methylene units largely affected the physical properties of CUPE, the choice of diol did not affect the overall polymer cell/tissue-compatibility both in vitro and in vivo. In conclusion, we have established the diol component as an important parameter in controlling the structure-property relationship of the polymer in addition to diisocyanate concentration and post-polymerization conditions. Expanding the family of CUPE polymers increases the choices of biodegradable elastomers for tissue engineering applications.     

Synthesis and Characterization of Some Triphenyltin(IV) Complexes from Sterically Crowded [((E)-1-{2-Hydroxy-5-[(E)-2-(aryl)-1-diazenyl]phenyl}methylidene)amino]acetate Ligands and Crystal Structure Analysis of a Tetrameric Triphenyltin(IV) Compound

Four new triphenyltin(IV) complexes containing [((E)-1-{2-hydroxy-5-[(E)-2-(aryl)-1-diazenyl]phenyl}methylidene)amino]acetate ligands (L) have been synthesized with formulations of Ph₃SnLH. They have been studied by multinuclear (¹H, ¹³C, ¹¹⁹Sn) NMR, ¹¹⁹Sn M?ssbauer and IR spectroscopy. A full characterization of one complex, Ph₃SnL¹H (1), was accomplished by single crystal X-ray crystallography, which revealed the compound to be a macrocyclic tetramer. In the tetramer, the five coordinate tin atoms have distorted trigonal bipyramidal geometries with the three phenyl groups occupying equatorial positions, while an oxygen atom of the carboxylate group of one L ligand and the oxide O-atom (formerly the hydroxy group) of a second L ligand in an apical positions. The carboxylate ligands bridge adjacent tin atoms and coordinate in the zwitterionic form with the phenolic proton moved to the nearby nitrogen atom. ¹¹⁹Sn NMR results indicate that the tetrameric structures of the complexes in the solid state, in which the tin atoms are five-coordinated, dissociate in solution to yield four coordinate monomeric species.