Theoretical Estimation of Changes in Plane Elastic Waves due to Cylindrical Inclusions

Changes in amplitude and phase shifts in plane elastic waves were theoretically estimated when they propagated through an elastic body containing cylindrical inclusions. Based on the integral equation suggested by Lavrov et al., these changes were calculated in the case when only one cylindrical inclusion was located in the body and the propagating waves have a single frequency. These calculations were expanded to more practical case when multiple cylindrical inclusions aligned in the body and the waves have some frequency band. The changes in amplitude and phase shifts calculated were associated to the changes in apparent sonic velocity and attenuation coefficient due to a structural change in the material. This theoretical approach contributes to a quantitative damage evaluation based upon structural changes in various materials by measuring the acoustical parameters such as apparent sonic velocity and attenuation coefficient.     

Microstructural degradation mechanisms during creep in strength enhanced high Cr ferritic steels and their evaluation by hardness measurement

There are two creep regions with different creep characteristics: short-term creep region “H”, where precipitates and subgrains are thermally stable, and long-term creep region “L”, where thermal coarsening of precipitates and subgrains appear. In region “H”, the normalized subgrain size (λ-λ₀)/(λ^∗-λ₀) has a linear relation with creep strain and its slope is 10ε⁻¹. But, region L is the time range in which the static recovery and the strain-induced recovery progress simultaneously. In this region, the static recovery accelerates the strain-induced recovery, and subgrain size is larger than that line which neglects the contribution of the static recovery. In region “L”, the Δλ/Δλ^∗-strain present a linear relation with a slope 35ε⁻¹. There is a linear relation between hardness and subgrain size. Hardness drop, H₀ − H, as a function of Larson-Miller parameter can be a good measure method for assessment of hardness drop and consequently degradation of microstructure. Hardness drop shows an identical slope in creep region “H”, whereas hardness drop due to thermal aging and creep in region “L” show together a similar slope. In region “H”, degradation of microstructure is mainly due to recovery of subgrains controlled by creep plastic deformation, and precipitates do not have a major role. However, in creep region “L”, there are three degradation mechanisms that accelerate creep failure; (1) strain-induced recovery of subgrains due to creep plastic deformation, (2) static-recovery of subgrains and precipitates and (3) strain-induced coarsening of precipitates due to the appearance of static-recovery.     

An experimental study on self-output-control characteristics of micro downwind rotor with coning soft blades

In this short paper,we have treated the aerodynamic performance of micro downwind rotor with coning soft blades experimentally.The test wind rotor has the tip diameter of 1.5 m and three two-dimensional NACA0018 blades of 0.15 m chord whose material is light,soft and pliable foam plastic for perfect safety.From the wind tunnel test,it is realized that the performance is manageable by the coning angle of the rotor blade.In the present case,an improvement of the performance in lower wind speeds is achieved by...     

Adsorption properties of amphiphilic polyoxyalkylenated dimethylpolysiloxane derivatives on keratin

Adsorption properties of two types of dimethylpolysiloxane backbone derivatives, perfluoroalkyl polyoxyethylenated dimethylpolysiloxane (FPD) and polyoxyethylenated dimethylpolysiloxane (PD), onto keratin surfaces were investigated. Both polymers are amphiphilic, since they possess hydrophilic polyoxyethylene groups. FPD contains a perfluoroalkyl group that provides both water-and oil-repellent properties, whereas PD lacks these groups. Adsorption properties of these polymers onto keratin surfaces are considered a good index to evaluate these compounds as nonionics used in hair-coating agents, since keratin is a major component of hair. FPD was more likely to be adsorbed and less likely to be eliminated from the keratin surface than PD. Once FPD had been adsorbed onto the keratin surface, it was very slowly washed from the surface when it was immersed in stationary water, whereas PD polymers were quickly washed from the keratin surface. Even in running water, rapid elimination of FPD was not observed. The strong resistance to loss of FPD after washing with a large quantity of water may be due to the water-repellent nature of the perfluoroalkyl groups. As a comparison, FPD adsorption onto a glass surface was also investigated. The affinity to the glass surface was found to be less than to the keratin surface.     

Transient power characteristics of balanced three‐phase variable inductance

Inductance has a particularly important role in power circuits. The authors have proposed the Variable Active–Passive Reactance (VAPAR), which can produce a virtual variable inductance. In this paper, the transient power characteristics of a balanced three‐phase variable inductance are analyzed using the instantaneous active and reactive power theorem. With an ideal voltage source or an ideal current source connected to a balanced three‐phase variable inductance, the transient power characteristics are analyzed theoretically, and then the results are verified through simulations. In the other cases, it is difficult to solve for the transient power, but it is shown that the transient power characteristics can easily be estimated from the results of simulations in which an ideal voltage source or an ideal current source is connected to a balanced three‐phase variable inductance. Experiments are also carried out to verify the theoretical analysis and simulations. © 2001 Scripta Technica, Electr Eng Jpn, 136(2): 49–57, 2001     

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.     

Charged ultrafiltration membrane for permeation of proteins

Polyacrylonitrile-g-poly(N,N-dimethylaminoethyl methacrylate) was synthesized photochemically and quaternized. The positively charged membranes made from the quaternized graftcopolymer showed high ultrafiltration rate for water by adding poly(vinyl alcohol) to casting solution and washing it out after the casting. In buffered saline solution, the permeability of the membranes was very small at pH below isoelectric point of albumin but increased markedly at higher pH. On the other hand, the permeability for γ-globulin was very small and did not show any pH dependence.     

Surface active N-acylglutamate: I. Preparation of long chain N-acylglutamic acid

Long chain N-acylglutamic acid was prepared in a high yield by a reaction of glutamic acid with fatty acid chloride in a mixed solvent of water and a water miscible organic solvent such as acetone, methyl ethyl ketone, dioxane, tetrahydrofuran,t-butyl alcohol or cyclohexanone. In this reaction the composition of the mixed solvent influenced the yield of N-acylated glutamic acid and the best yield was obtained when the reaction was carried out in the mixed solvent comprising 30–60% v/v of the organic solvent. Long chain N-acylaspartic acid was also obtained in a high yield by the same method. As the other method to obtain N-lauroyl-D L-glutamic acid, it was examined that N-acyl-α-aminoglutarodinitrile which was obtained by a reaction of α-aminoglutarodinitrile with fatty acid chloride was hydrolyzed with an aqueous alkaline solution. The salts of long chain N-acylglutamic acid are known as the surface active agents that react mildly on the human skin.