An image processing system using Image Signal Multiprocessors (ISMPs)

This paper describes an image processing system using Image Signal Multiprocessors (ISMPs) adapted to gray-level image preprocessing for image analysis and image enhancement. It is composed of four ISMPs, five 1H-delay-lines, two 512×512×8-bit frame memories, a video timing controller (VTC), two 256-word ×8-bit ×8-table Look Up Tables (LUTs) and 80 nsec/sampling A/D and D/A converters. This multiprocessor system performs convolution operations such as spatial filters, contrast enhancement, and binarization for gray-level images, thinning, thickening, pattern matching etc. for binary images, and image quality improvement for moving images such as T.V. images. Otherwise, it performs feature extraction operations such as area calculations, fillet coordination, and moment calculations for objective image data. Moreover, this system is capable of applying color image processing by using a multiboard system.     

New technique for bonding hydroxyapatite ceramics and magnesium alloy by hydrothermal hot-pressing method

The solidification of hydroxyapatite (HA:Ca₁₀(PO₄)₆(OH)₂) and its bonding with Magnesium (Mg) alloys (AZ31; Mg–3Al–1Zn) were achieved simultaneously by using a hydrothermal hot-pressing method at a low temperature as low as 150 °C with no special surface treatment of Mg alloy. A mixture of calcium hydrogen phosphate dihydrate and calcium hydroxide was used as a starting powder material for solidifying HA. 3-point bending tests were conducted to obtain an estimate of the fracture toughness for the HA/Mg interface as well as for the HA ceramics only. The fracture toughness tests showed that the induced crack from the pre-crack tip deviated from the HA/Mg interface and propagated into the HA. The fracture toughness determined on the bonded HA/Mg specimen was close to that of the HA ceramics only (0.30 MPam^1/2).     

High-temperature pyrolysis of ceramic fibers derived from polycarbosilane–polymethylhydrosiloxane polymer blends with porous structures

The polymer blends of PCS (polycarbosilane) and PMHS-h (polymethylohydrosiloxane with high molecular weight) were prepared by freeze-drying process of mixed benzene solution. Melt viscosity, mass loss, and gas evolution from prepared polymer blends were analyzed. A polymer blend of HSah15 (15 mass% PMHS-h to PCS) was melt-spun to fiber form, curing by thermal oxidation and pyrolyzed at various temperatures up to 1773 K. The obtained fibers were investigated by tensile tests, FE-SEM (field emission scanning electron microscope) observation, and XRD (X-ray diffraction) analysis. After pyrolysis at 1273 K, there were no pores in the cross section of the fiber derived from pure PCS; however, there were amounts of pores in the cross sections of the fiber derived from HSah15. After pyrolysis at 1773 K, the coarse β-SiC (silicon carbide) crystals were formed on the outside surface of the fiber derived from pure PCS; however, no remarkable β-SiC crystal were formed on the outside surface of the fiber derived from HSah15.     

Structurally Diverse Polyamines: Solid‐Phase Synthesis and Interaction with DNA

A versatile solid‐phase approach based on peptide chemistry was used to construct four classes of structurally diverse polyamines with modified backbones: linear, partially constrained, branched, and cyclic. Their effects on DNA duplex stability and structure were examined. The polyamines showed distinct activities, thus highlighting the importance of polyamine backbone structure. Interestingly, the rank order of polyamine ability for DNA compaction was different to that for their effects on circular dichroism and melting temperature, thus indicating that these polyamines have distinct effects on secondary and higher‐order structures of DNA.     

Modulation of nanotube formation in apatite single crystal via organic molecule incorporation

Hydroxyapatite materials are potentially useful for biomedical application, especially as vehicles for functional molecules. Structural control of bulk apatite materials, such as in the fabrication of hollow microspheres or porous structures, has been studied for this purpose. However, control of the internal structure of the source apatite crystal itself is still a challenge. Here, we show that small organic molecules incorporated in apatite crystals act as porogens which control the porous structure of apatite single crystal. The presence of amino acid under apatite synthesis conditions leads to firm bindings and encapsulation of the amino acid in apatite single crystals. Amino acid elimination by heating or electron beam irradiation enhances the pore formation in apatite single crystal. Moreover, incorporation of an acidic amino acid in apatite induces peapod like nanotubes in apatite single crystals. This study suggests the potential of using small organics for nano-structural control of apatite single crystals which would be valuable for enhancing drug loadings or modulating material digestion in vivo.     

Phase equilibrium of the VSe2/1bV3Se4 system and the thermodynamic quantities of the V3Se4 phase

The equilibrium selenium vapour pressure of V_xSe₂ (1.2 < x < 1.7) was measured by a thermobalance method at 1053, 1113 and 1163K under controlled selenium vapour pressure. The thermodynamic partial molar quantities of the V₃Se₄ phase were evaluated from the measured P_Se- X isotherms. Further, the powder X-ray and high temperature DTA measurements of the quenched specimens were carried out in order to identify the phase.     

Characterization of the layered transition-metal dichalcogenides with octahedral coordination

The lattice constants of nonstoichiometric CdI₂-type transition-metal dichalcogenides exhibit a characteristic feature. One of the body-diagonal lengths of the hexagonal lattice is kept nearly constant over the homogeneity range. This body-diagonal direction involves the full-layer metal-chalcogen bonds. The heats of formation of various CdI₂-type transition-metal dichalcogenides are correlated to the reduced length which is derived from that body-diagonal and the ideal ionic radii. The ΔH^o_f values of the CdI₂-type transition-metal dichalcogenides can be estimated from the following empilical formula within the error of about 10kcal/mole. ΔH^o_f = 1030 L_R ? 144 (kcal/mole). L_R: Reduced length.     

Morphologic Control of Pt Supported Titanate Nanotubes and Their Photocatalytic Property

Morphologic control of Pt supported titanate nanotubes was attempted by the hydrothermal hot-pressing (HHP) technique in order to improve the handleability as a photocatalyst. The bulk of Pt-nanocrystal supported titanate nanotubes was successfully fabricated without the H₂ reduction process by applying the HHP technique. The bulky Pt-nanocrystal supported titanate nanotubes possessed dense microstructures, significantly sharp distributions of mesopores, and high Brunauer–Emmett–Teller (BET) surface area. Furthermore, the bulky Pt-nanocrystal supported titanate nanotubes showed the photocatalytic degradation activities of 2-propanol aqueous solution under UV-light irradiation.     

Influence of ion assistance on LaF3 films deposited by molybdenum boat evaporation

LaF3 thin films at 193 nm were deposited by the molybdenum boat evaporation with ion-assisted deposition (IAD). Various optical characteristics, stress, and microstructures that formed under different ion-beam voltages of IAD deposition were investigated. The relation between these properties is also discussed. LaF3 films deposited with IAD exhibited small rough surfaces and large optical loss at 193 nm. The largest value of optical loss for films at 193 nm, which were prepared at an ion-beam voltage of 400 V, was 1.55% and the extinction coefficient was smaller than 0.0015. Microstructures and crystalline structures of films were influenced and changed by the ion-assisted deposition process. Tensile stress value of films increased as the ion-beam voltage rose. Refractive index, related to the packing density and microstructures, also increased as the ion-beam voltage rose.