Effect of hardness difference on the surface durability and surface failure of steel rollers

Experiments with pairs of rollers of different hardnesses designed to assess the effect of hardness difference on surface durability and surface failure are described. Sliding-rolling contact fatigue tests were performed with combinations of thermally refined, through-hardened and induction-hardened 0.45% C steel rollers. The mode of failure is discussed in relation to the hardness difference between the rollers and the presence of residual stresses. The effect of hardness on the modulus of elasticity was also examined. An empirical equation was devised to describe the relationship between the rolling contact fatigue limit under hertzian stress and the surface hardness.     

Fiber volume control of composite materials by loss angle

Fiber volume plays a critical role in achieving stable mechanical and physical properties in composite structures. This study develops a method to control this parameter in carbon fiber reinforced plastics (CFRPs) on the basis of the viscoelastic character of the thermosetting matrix resin. This method relies on the loss angle δ to quantitatively control fiber volume. CFRP flat panels are manufactured at varying initiating times of pressure application depending on the δ value of the CFRP matrix resin. An analysis of the manufactured panels clearly shows that the target fiber volumes can be obtained at an appropriate δ range. Specifically, CFRP fiber volumes can be controlled through the loss angle of the matrix resin. Defining this δ range is very important for establishing mechanically and physically stable CFRP structures. POLYM. COMPOS., 37:1307–1311, 2016. © 2014 Society of Plastics Engineers     

A New Equation for Predicting the Dielectric Constant of a Mixture

The dielectric constant of a compound consisting of two different materials was simulated using the Monte Carlo and finite element methods. In the high concentration range of the higher dielectric constant material, the simulated value of the dielectric constant showed a "parallel-model"-like tendency. On the other hand, in the low concentration range of the higher dielectric constant material, the compound showed a "serial-model"-like behavior. Around 65% content of the higher dielectric constant material, it exhibited results similar to the logarithmic mixing rule. After careful consideration of these results, a new equation to predict the dielectric constant of the compound was derived. The agreement between the dielectric constant calculated by the new equation and the measured values was better than in any other case reported before.     

Compression Deformation Mechanism of Silicon Carbide: I, Fine-Grained Boron- and Carbon-Doped β-Silicon Carbide Fabricated by Hot Isostatic Pressing

The deformation behavior of boron- and carbon-doped β-silicon carbide (B,C-SiC) with an average grain size of 260 ± 18 nm containing 1 wt% boron was investigated by compression testing at elevated temperatures. Extensive grain growth during deformation was observed. The stress–strain curves were compensated for grain growth by assuming power-law type of dependence on grain size and strain rate. The stress exponent n was ∼1.3 and the grain size exponent p was ∼2.7 at temperatures ranging from 1593° to 1758°C. The apparent activation energy of deformation Q _d was ∼760 kJ/mol, which was lower than the activation energy for lattice diffusion of silicon and carbon in SiC and higher than that for grain-boundary diffusion of carbon in SiC. These results suggest that the deformation mechanism of the fine-grained B,C-SiC is grain-boundary sliding accommodated by the grain-boundary diffusion.     

Effect of surface properties of silica nanoparticles on their cytotoxicity and cellular distribution in murine macrophages

In this study, complexes composed of poly-l-tyrosine (pLT) and single-walled carbon nanotubes (SWCNTs) were produced and the dispersibility of the pLT/SWCNT complexes in water by measuring the ζ potential of the complexes and the turbidity of the solution were investigated. It is found that the absolute value of the ζ potential of the pLT/SWCNT complexes is as high as that of SWCNTs modified with double-stranded DNA (dsDNA) and that the complexes remain stably dispersed in the water at least for two weeks. Thermogravimetry analysis (TGA) and visualization of the surface structures of pLT/SWCNT complexes using an atomic force microscope (AFM) were also carried out.     

High-efficiency GaAs and GaInP solar cells grown by all solid-state molecular-beam-epitaxy

We report the initial results of GaAs and GaInP solar cells grown by all solid-state molecular-beam-epitaxy (MBE) technique. For GaAs single-junction solar cell, with the application of AlInP as the window layer and GaInP as the back surface field layer, the photovoltaic conversion efficiency of 26% at one sun concentration and air mass 1.5 global (AM1.5G) is realized. The efficiency of 16.4% is also reached for GaInP solar cell. Our results demonstrate that the MBE-grown phosphide-contained III-V compound semiconductor solar cell can be quite comparable to the metal-organic-chemical-vapor-deposition-grown high-efficiency solar cell.     

Nanocomposites derived from cellulose acetate and highly branched alkoxysilane

Highly branched alkoxysilane (HB) units were prepared in situ via a Michael‐type reaction between pentaerythrithol triacrylate and aminopropyltriethoxysilane. These units were used as an inorganic component for the modification of cellulose acetate (CA) films using the sol–gel process. The thermal and dynamic‐mechanical behaviors, the morphology, and the dimensional stability of the modified CA films were analyzed. The siloxane‐modified CA films showed thermal stability similar to pure CA, but the residue content at 900°C increased with the addition of HB units. The morphology of these films was characterized by siloxane nanodomains dispersed in the CA matrix, with good interfacial adhesion between the phases. Moreover, the CA/siloxane nanocomposite films showed improved dimensional stability in comparison with CA, i.e., in the presence of HB, the dimensional change was reduced to around 50% of the value observed for pure CA. Finally, a complex dynamic‐mechanical behavior was obtained for the nanocomposite films, as a consequence of the heterogeneous morphology. © 2011 Wiley Periodicals, Inc. J Appl Polym Sci, 2011