Effect of W-Mo balance and boron nitrides on creep rupture ductility of 9Cr steel

The effect of W-Mo balance and boron nitrides (BN) on creep rupture ductility has been investigated for five heats of 9% Cr steel with 1.5% Mo equivalent, 0.003% boron and 0.05% nitrogen at 600^oC, 650^oC and 700^oC. The maximum time to rupture was 68,718 h at 650^oC. The reduction of area (RA) slightly decreases for up to about 8000 and 1000 h at 600 and 650^oC, respectively, while it significantly decreases above those. The BN particles are responsible for the degradation in RA at low stresses and long times by accelerating the formation of creep voids. At high stresses and short times, the RA decreases with increasing time to rupture and with increasing W concentration and concomitantly with decreasing Mo concentration. The rupture ductility is evaluated by using a semi-logarithmic diagram of the RA and total elongation, showing the necking dominant and void swelling dominant regions.     

Microstructural change of ultrafine-grained aluminum during high-speed plastic deformation

Effect of strain rate on microstructural change in deformation of the ultrafine grained (UFG) aluminum produced by severe plastic deformation (SPD) was studied. Commercial purity 1100 aluminum sheets were highly strained up to an equivalent strain of 4.8 by the Accumulative Roll-Bonding (ARB) process at ambient temperature. The ARB-processed sheets were found to be filled with pancake-shaped ultrafine grains surrounded by high-angle grain boundaries. The ultrafine grains had a mean grain thickness of 200 nm and a mean grain length of 1100 nm. The ultrafine-grained aluminum sheets were deformed at various strain rates ranging from 2 to 6.0×10⁴ s⁻¹ by conventional rolling, ultra-high-speed rolling, and impact compression. High-speed plastic deformation generates a large amount of heat, inducing coarsening of the ultrafine grains during and after deformation. On the other hand, it was also suggested that high-speed plastic deformation is effective for grain-subdivision, in other words, ultra-grain refinement, if the effect of heat generation is extracted.     

Effect of fiber array irregularities on microscopic interfacial normal stress states of transversely loaded UD-CFRP from viewpoint of failure initiation

A detailed investigation has been carried out to determine the effect of local fiber array irregularities and controlling fiber distribution parameters on microscopic interfacial normal stress states for transversely-loaded unidirectional carbon fiber (CF)/epoxy composites. Linear elastic finite element analyses were carried out for two-dimensional image-based models composed of about 70 fibers. The relationship between the geometrical distribution of two adjacent fibers and the interfacial normal stresses (INSs) is investigated for all fibers in different image-based models. Three boundary conditions for loading were selected: Case A involved cooling from the curing temperature (the difference in temperature was ?155 K); Case B involved transverse loading of 75 MPa chosen as an example of macroscopic transverse fracture strength; and Case C involved both cooling from the curing temperature and transverse loading of 75 MPa. High compressive INSs due to the difference in the coefficients of thermal expansion are observed at the location of the shortest interfiber distance for Case A (cooling). High tensile INSs are observed at the location of the shortest interfiber distance and where the fiber alignment angle to the loading direction is small for Case B (loading). For Case C (cooling and loading), the high thermal residual compressive INSs and the high mechanical tensile INSs compensate each other, and the INSs at a short interfiber distance are much lower than those for Case B. These results clearly indicate the importance of the contribution of the thermal residual stresses to the transverse tensile failure initiation of CF/epoxy laminates.     

ESR and Mössbauer studies of the precipitation process of various ferrites from silicate glasses

ESR and Mössbauer studies of the precipitation process of various ferrites from silicate glasses were made to characterize the precipitation mechanism. The changes in linewidth (H _1/2) and effectiveg-value (g _eff) in the ESR spectra of the precipitation process are well explained in terms of super-exchange interaction between magnetic ions and interparticle dipolar interaction between precipitated ferrites. The precipitation tendency of spinel type ferrites from silicate glasses was found to be in the following order: NiFe₂O₄CoFe₂O₄>Fe₃O₄ZnFe₂O₄, MnFe₂O₄. The above order coincided with the order of octahedral site preference energies of divalent transition metal ions.     

Automated single nucleotide polymorphism typing using bead array in capillary tube

A low-cost and simple on-site technique for genotyping single nucleotide polymorphisms (SNPs) was developed. The technique is based on allele-specific primer PCR and the recently developed bead arrays in a single tip technique. The performance of the method was verified by genotyping four SNPs that correlate with cardiovascular diseases.     

Interaction of π-bonds of the silicon–silicon triple bond with alkali metals: An isolable anion radical upon reduction of a disilyne

The reduction of 1,1,4,4-tetrakis[bis(trimethylsilyl)methyl]-1,4-diisopropyltetrasila-2-yne 1 with an equivalent amount of alkali metal (Li, Na, K, KC₈) in THF produced the corresponding disilyne anion radicals 2a–c. Their EPR spectra are independent of the metals used in THF, indicating that the disilyne anion radical species exists as solvent-separated ion pairs in polar solvents. The one-electron reduction also occurred with potassium in toluene to produce the potassium salt of the anion radical 3, which was isolated as extremely air- and moisture-sensitive dark brown crystals. The molecular structure of 3 was established by X-ray crystallography, which showed that the potassium ion is solvated by one toluene molecule. The EPR spectrum of 3 in toluene showed the interaction of the anionic silicon atom with the K⁺ ion.     

Control of carbon incorporation in AlAs grown by atomic layer epitaxy using variously orientated substrates

We demonstrate a method for successfully controlling carbon incorporation in AlAs layers grown by atomic layer epitaxy (ALE) using various GaAs substrates with different orientations. The number of alkyl radicals attached to an Al atom at the surface, which is a main factor in carbon incorporation, can be intentionally controlled by changing substrate orientation. We found that the carbon incorporation in ALE-AlAs using the (3 1 1)B surface is 2 x 10¹⁷,cm^-3, which is the lowest value ever reported for ALE-AlAs that satisfies one-monolayer self-limiting growth conditions.     

Pb-free surface-finishing on electronic components’ terminals for Pb-free soldering assembly

Pb-free solderable surface finishing is essential to implement Pb-free solder assembly in order to meet with the growing demand of environmental consciousness to eliminate Pb from electronic products. Two types of widely applicable Pb-free surface finishing technologies are developed. One is the multilayer-system including Pd with Ni undercoat. Heat-resistance of Pd enables whole-surface-plating on to leadframe before IC-assembling process. The other is the double-layer-system with low-melting-point-materials, for example, thicker Sn underlayer and thinner Sn-Bi alloy overlayer, dilutes Sn-Bi alloy’s defects of harmful reactivity along with substrate metal and mechanical brittleness with keeping its advantages of solder-wettability and no whisker.     

Programmed High‐Hole‐Mobility Supramolecular Polymers from Disk‐Shaped Molecules

In this paper a simple, casting solution technique for the preparation of two‐dimensional (2D) arrays of very‐high molecular weight (MW) 1D‐Pc supramolecular inorganic polymers is described. The soluble fluoroaluminium tetra‐tert‐butylphthalocyanine (ttbPcAlF) is synthesized and characterized, which can be self‐assembled to form 2D arrays of very‐high‐MW 1D‐Pc supramolecular inorganic polymers. High‐resolution transmission electron microscopy (HRTEM) demonstrates that the 1D‐ttbPcAlF, having a cofacial ring spacing of ～0.36 nm and an interchain distance of ～1.7 nm, self‐assembles into 2D‐nanosheets (～140 nm in length, ～20 nm in width, and equivalent to MW of 3.2 × 10⁵ g mol^?1). The film cast from a 1,2‐dichloroethane (DCE) solution shows a minimum hole‐mobility of ～0.3 cm² V^?1 s^?1 at room temperature by flash‐photolysis time‐resolved microwave conductivity (TRMC) measurements and a fairly high dark dc‐conductivity of ～1 × 10^?3 S cm^?1.