Cellular array processor CAP and applications

The general-purpose, highly parallel, cellular array processor (CAP) we developed features multiple-instruction stream, multiple-data stream (MIMD) processing and image display. Processor elements can number in several hundreds. The present system uses 256 processors. Each processor element consists of a general-purpose microprocessor, memory, and a special VLSI chip that performs parallel-processing-specific functions such as processor communication and synchronization. The VLSI has two 2M byte/s independent common bus interfaces for data broadcating and six 15M bit/s serial communication ports for local data communication. The chip also can process image data in real time for multiple processors. Use of the communication interfaces enables a variety of processor networks to be configured. One CAP application has been computer graphics, in which ray tracing is used to generate quality images.     

Dissolution and Absorption of Nipedipine from Nifedipine-Polyvinylpyrrolidone Coprecipitate

Attempt was made to develop the solid dosage form of nifedipina which showed good absorption rate and total bioavailability. Nifedipine is a poorly water-saluble drug, whom bioavailability is low when administered orally in the crystalline form. Solutions of nifedipine were well absorbed from the gastrointestinal tract. The dissolution rate of PVP-nifedipine coprecipitates exhibited rapid dissolution rate. X-ray diffraction data suggested the lack of crystallinity in the coprecipitate. The relation between the dissolution rates and average molecular weights of PVP was studied. Nifedipine in the copretipitate was chemically stable to heat and humidity, but the dissolution rate of nifedipine from the coprecipitate stored at 21° and 75% R.H. markedly decreased. X-ray diffraction data revealed that it might be due to the transformation of amorphous form of nifedipine to crystalline form under higher relative humidity. The gastrointestinal absorption of nifedipine in beagle dogs after oral administration of the coprecipitate was increased than that after oral adniniatration of the physical mixture.     

Creep strength of magnesium-based alloys

The high-temperature creep resistance of magnesium alloys was discussed, with special reference to Mg-Al and Mg-Y alloys. Mg-Al solid-solution alloys are superior to Al-Mg solid-solution alloys in terms of creep resistance. This is attributed to the high internal stress typical of an hcp structure having only two independent basal slip systems. Although magnesium has a smaller shear modulus than aluminum, the inherent creep resistance of Mg alloys is better than that of Al alloys. The creep resistance of Mg alloys is improved substantially by the addition of Y. Solid-solution hardening is the principal mechanism of the strengthening, but the details of the mechanism have not been elucidated yet. Forest dislocation hardening in concentrated alloys and dynamic precipitation in a Mg-2.4 pct Y alloy also contribute to the strengthening. An addition of a very small amount of Zn raises the dislocation density and significantly improves the creep resistance of Mg-Y alloys. This article is based on a presentation made in the symposium entitled “Defect Properties and Mechanical Behavior of HCP Metals and Alloys” at the TMS Annual Meeting, February 11–15, 2001, in New Orleans, Louisiana, under the auspices of the following ASM committees: Materials Science Critical Technology Sector, Structural Materials Division, Electronic, Magnetic & Photonic Materials Division, Chemistry & Physics of Materials Committee, Joint Nuclear Materials Committee, and Titanium Committee.     

Electron spin resonance investigation of small spin probes in aqueous and vesicle phases of mixed membranes made from poly(oxyethylene) hydrogenated castor oil and hexadecane

Small spin probes in the vesicle and aqueous phases of mixed membranes made from poly(oxyethylene) hydrogenated castor oil (HCO) and hexadecane were investigated by ESR (electron spin resonance) spectroscopy. Partitioning (partition coefficients), rotational correlation times, and activation energies of the spin probes in the vesicle phase were determined. The quantitative results obtained by an ESR simulation indicated that the spin probe DTBN (di-tert-butyl nitroxide), in the vesicle of the mixed membrane, was partitioned similar to that of TEMPO (2,2,6,6-tetramethylpiperidine-1-oxyl) at 50 degrees C, and the partitioning for both probes showed no abrupt change across the temperatures examined. The results differed considerably from conventional analyses of the high-field signal intensities. Activation energies obtained by the simulation for DTBN and TEMPO were 21 and 20 kJ/mol, respectively. In addition, the hyperfine values of 15.8 (DTBN) and 16.1 G (TEMPO) in the vesicle phase were consistent with the activation energies and supported the probe environments in the membrane. Thus, the present ESR results provided detailed information regarding the probe behavior in the membrane.     

High-speed digital-signal transmission experiments by optical wavelength-division multiplexing

The letter reports results obtained with laboratory transmission experiments on high-speed digital signals by optical wavelength-division multiplexing, using a newly developed optical multiplexer and demultiplexer, as well as other high-performance optical devices and fibres.     

Preparations and reactions of alkyl ethers of some aldohexoses

Aldohexose, such asd-glucose,d-galactose ord-mannose, reacted with acetone to give the following O-isopropylidene derivatives: 1,2;5,6-di-O-isopropylidene-d-glucofuranose (IA), 1,2;3,4-di-O-isopropylidene-d-galactopyranose (IB) or 2,3;5,6-di-O-isopropylidene-D-mannofuranose (IC). The O-isopropylidene derivative (IA～IC) reacted with alkyl/alkenyl halogenide to yield aldohexose ether compounds containing di-O-isopropylidene group, 3-O-alkyl-1,2;5,6-di-O-isopropylidene-d-glucofuranose (II), 6-O-alkyl-1,2;3,4-di-O-isopropylidene-d-galactopyranose (III) or 1-O-alkyl-2,3;5,6-di-O-isopropylidene-d-mannofuranoside (IV), in good yields. The Williamson ether synthesis was carried out using phase-transfer catalysis (PTC). The derived aldohexose alkyl ether containing di-O-isopropylidene group was hydrolyzed to give 3-O-alkyl-1,2-O-isopropylidene-d-glucofuranose (V) as a partial hydrolysis product; the complete hydrolysis of I～IV gave, as expected, 3-O-alkyl-glucopyranose (VI), 6-O-alkyl-galactopyranose (VII) or 1-O-alkyl-mannofuranoside (VIII). Further alkylation of (V) with Mel under PTC and subsequent acid hydrolysis gave 3-O-alkyl-5,6-di-O-methyl-d-glucofuranose (X). Methanolysis of III with catalytic amounts of H₂SO₄ gave 1-O-methyl-6-O-alkyl-d-galactofuranoside (XI). The elucidation of the galactofuranoside skeleton of (XI) was determined by means of its¹³C nuclear magnetic resonance spectra. The O-alkyl aldohexoses, e.g., X and XI, were evaluated and found to be emulsifiers.     

Radiation-induced polymerization of ethylene in a pilot plant. I. Bulk process

Radiation-induced bulk polymerization of ethylene was carried out with use of a pilot plant with a 10 liter reactor at pressures of 225–400 kg/cm², temperatures of 30–95°C, ethylene feed rates of 5–28 kg/hr, and dose rate of 3.8 × 10⁵ rad/hr. Characteristics of the process are mild polymerization conditions and capability of producing medium density polyethylene in powder form. The spacetime yield and molecular weight of polymer were in the range of 3.5 to 13.1 g/liter hr and 2.2 × 10⁴ to 14 × 10⁴, respectively. The space-time yield increased with mean residence time and 2.4 powders of pressure, and decreased with temperature. Molecular weight changed similarly with the reaction conditions. These results were consistent with those of the bench plant experiment and the scale effect was small. Polymer deposit to the reactor wall limited a period of continuous operation of the plant. The amount of deposited polymer was increased with the square of reaction time. The rate of polymer deposit was proportional to polymer concentration and to the cube of pressure. The polymer deposit cannot be solved in the bulk process.     

Growth of High-Quality Pb((Zn1/3Nb2/3)0.91Ti0.09)O3 Single Crystals by Excess ZnO Addition

A high-quality single crystal of Pb((Zn_1/3Nb_2/3)_0.91Ti_0.09)O₃ (PZNT 91/9), 40 mm in diameter and 20 mm in length, was successfully grown using the solution Bridgman method with a slight excess amount of ZnO. High-quality wafers were sliced from the light-brown single crystal. No PbO inclusions or opaque areas were observed in the transparent wafers. An array probe for echocardiography was constructed with the single-crystal wafer, and its superior performance was demonstrated.     

Electron spin resonance of transparent alumina ceramics fabricated by spark plasma sintering

Transparent α‐alumina ceramics are fabricated using spark plasma sintering. Paramagnetic defects related to the optical properties of the ceramics have been investigated using electron spin resonance (ESR) analyses. An isotropic ESR signal at g = 2.003 (S = 1/2) with a linewidth of 0.5 mT is formed during sintering. The g = 2.003 signal intensity has a weak correlation with the absorbance in the visible region but does not correlate with the real in‐line transmission (RIT) at 650 nm. An ESR signal with a fine structure attributed to Fe³⁺ was detected in both the α‐Al₂O₃ starting powder and the sintered ceramic samples. The degree of c‐axis orientation of the grains has been determined using the Fe³⁺ signal intensity, which depends on the angle between the directions of the c‐axis and the applied magnetic field. The ESR analysis indicated that the c‐axis tends to be oriented in the direction of the sintering pressure. The degree of c‐axis orientation was found to correlate with the RIT in highly densified ceramics.     

Spin-Probe Investigations of Head Group Behavior in Aqueous Dispersions of a Nonionic Amphiphilic Compound

Head group behavior of nonionic amphiphilic compound, (poly(oxyethylene) hydrogenated castor oil, HCO), in aqueous dispersions were investigated by EPR (electron paramagnetic resonance) in conjunction with a modern slow-tumbling simulation. The aliphatic spin probes, 5-doxylstearic acid (5-DSA) and 3β-doxyl-5α-cholestane (CHL), were used to obtain fluidity of the surface region of the membrane. The order parameter (S ₀) using the simulation for 5-DSA and CHL in the region were approximately 0.4 and 0.2, respectively. The ordering results suggest that the head group region of the membrane is somewhat fluid. The rotational diffusion coefficients (R _⊥ ≈ 1/(6τ_R)) for the probes were 3.4 × 10⁷ and 7.1 × 10⁷ s⁻¹, respectively. Activation energies, calculated using the temperature dependence of diffusion coefficients, were 18 and 17 kJ/mol for the probes. The EPR results imply that the CHL probe in the HCO membrane has quite different behavior in comparison with that of PC (phosphatidylcholine) from egg. Thus, the present EPR analyses have provided quantitative insight into the surface region of the amphiphilic membrane.