Thermogravimetric Study of the M-Co-O System: I, M = Ta and Nb at 1200°C

Phase equilibria in the Ta-Co-O and Nb-Co-O systems have been studied at 1200°C at oxygen partial pressures from 10^−0.68 to 10^−13.50 atm for the former and from 10^−0.68 to 10^−13.30 atm for the latter. In both systems, M₂CoO₆ and M₂Co₄O₉ are stable ternary compounds under the experimental conditions, and a new phase, Nb₅Co₂O₁₄, has been identified. The Ta-Co-O system is simple, whereas the Nb-Co-O system is somewhat more complicated because of the extra phase. The lattice constants of the ternary compounds have been determined and compared with previous values. The standard Gibbs energies of reactions have been determined using oxygen partial pressures in equilibrium with three solid phases.     

Hydrodynamic interaction and coalescence of two droplets under large step shear strains

We observed change in distance between two droplets in each step after application of large multi-step shear strains. Experiments were performed using a sliding plate apparatus. Large step shear strains were applied to two polyisobutylene droplets in poly(dimethyl siloxane) matrix in the same plane between the plates. The distance between the two droplets decreases with increasing the total shear strain, which is given by the product of the step strain magnitude and the number of application of the step strains. The two droplets coalesce when the distance becomes less than the diameter of the droplets. The slope for plots of the distance versus the total strain is independent of the step strain magnitude. This indicates that the effect per unit strain on the distance is the same, irrespective of the strain magnitude. It is suggested that a stronger hydrodynamic interaction between the droplets is the main cause for the droplet approach.     

Frequency response function of magnetic bearings using high-temperature superconductor

A high-temperature superconductor YBa₂Cu₃O_7-x with strong pinning force has allowed stable magnetic suspension with no control to be developed. Two types of superconducting magnetic bearings (SMB) using YBCO and permanent magnet were assembled. The two types are radial and axial. The dynamic stiffness of each SMB as it was cooled down under a magnetic field by liquid nitrogen was measured both radially and axially. As a result, it was found that the spring constants of these SMBs were almost as large as a practically desirable value; however, their damping coefficients were lower than the practical level. These findings are useful as one of the data bases for development of an optimum SMB design to support the weight of rotors in an axial direction.     

Novel UV absorbers prepared from 2,4-dihydroxybenzophenone and hexachlorocyclotriphosphazene

The UV-stabilizing ability and thermal loss from the polystyrene film of novel UV absorbers, 2-[(3-hydroxy-4-benzoyl) phenoxy] pentachlorocyclotriphosphazene (HBPC) and hexakis[ (2-hydroxy-4-benzoyl) phenoxy] cyclotriphosphazene (HBPP), were investigated. The UV-stabilizing ability of HBPC estimated by the formation of carbonyl groups in polystyrene was comparable to that of 2,4-dihydroxybenzophenone (DHB), suggesting that the phosphazene moiety does not affect the efficiency of the stabilizing ability of DHB units. No significant difference of efficiency per stabilizing units between HBPC and HBPP was observed. HBPC and HBPP are noteworthy for their low thermal losses from the polystyrene film, i.e., the thermal loss of HBPP was completely suppressed and the diffusion coefficient of HBPC at 160°C was two orders of magnitude smaller than that of DHB. The thermogravimetric analysis and differential scanning calorimetry measurement showed that HBPC and HBPP are nonvolatile and stable up to 230 and 300°C, respectively. © 1993 John Wiley & Sons, Inc.     

IR reflection spectra of the silicate surface layer of yellowed rice plant leaf

We have investigated the IR reflectional properties of the three-hold cytrogical surface layer (kutchikura layer on silicate layer n(SiO₂) on silicate cellulose layer C₆H₁₀Si_xO_y) and that of chlorophyll, a(C₅₅H₇₂M_gN₄O₅) etc., present in bladder's cells by using our experimental method. From analysis of three set of anisotropical reflection spectra assigned as due to CO, SiO and NC surface oscillators contained in the cytrogical cells and measured at 2500 2200 cm^?1, 1200 700 cm^?1 and at 700 200 cm^?1 regions, we have confirmed some important results. One is their quantized directional distributions that of the numbers of fine step spectrum and that of the reflection integrals of these spectra. Here, that of the NC oscillators were found to distribute in pentagonal directions relating to the molecular structure of chlorophyll. Second, we confirmed the pecularity of eight fine step-series measured in these sensitive spectra comparing with that of bamboo's seven series. Third, from analysis of the stepnized variation of the “reflection integrals”, we estimated the origin of this effect as which is presumably due to statistical, transfer of the 2p₄ valence electrons etc. in the oxygen atoms from C=O, Si=O double bonding side upto the shallower quantized states, E(N,J) which were formed softly around the and surface oscillators. And these surface oscillators were confirmed as to make photo-chemical reaction process by receiving energy higher than ～24 m eV especially under the illumination of sunshine etc.     

Different feeding and gustatory responses to ecdysone and 20-hydroxyecdysone by larvae of the silkworm,Bombyx mori

The feeding and gustatory responses to ecdysone and 20-hydroxyecdysone were investigated in the silkworm,Bombyx mori. 20-Hydroxyecdysone reduced feeding response strongly in fourth- and fifth-instar larvae, whereas ecdysone had no effect on feeding response. 20-Hydroxyecdysone stimulated the R receptor, the receptor to feeding deterrents, to a great degree. By contrast, ecdysone was much less effective for stimulating the R receptor. These results indicate that ecdysone and 20-hydroxyecdysone have different effects on feeding response due to different interactions with mouthpart chemoreceptors.     

Polyacrylonitrile/Nylon 6 Blends: Preparation and Characterization

Summary: Polyacrylonitrile (PAN) particles with micro‐size ranges (0.15–2 μm) were prepared by emulsion and dispersion polymerizationa and in supercritical carbon dioxide media. The PAN particles were blended with Nylon 6 (PA6) at 220 °C by using a miniature mixer; it was found that melt‐mixing was possible for PAN‐rich compositions as high as 70 wt.‐%. Blends were characterized by scanning electron microscopy, IR, viscosity measurements, differential scanning calorimetry, and dynamic mechanical thermal analysis (DMTA). The size and shape of original PAN particles were retained in PAN/PA6 blends. The useful range to blend PAN particles size was less than 1 μm in terms of shape retention of the PAN particles in blends. Blends with 40 wt.‐% PAN content were found to be melt‐processable. The elastic modulus was higher for PAN/PA6 blends than pure PA6.

SEM photograph of PAN‐SC/PA6 blend with a 40/60 weight ratio.     

Synthesis of polyoxyethylene derivatives of diesters of sucrose with long-chain fatty acids

Summary Since the long-chain fatty acid sucrose diesters inevitably produced in the synthesis of monoesters are only slightly soluble in water, no important use can be found for them at the present time except as oilsoluble emulsifying agents. In order to exploit new uses we have attempted to improve their solubility in water by introducing oxyethylene radicals into the molecule. The addition reaction of ethylene oxide with the sucrose diesters was carried out in an autoclave in the presence of alkaline catalysts. With the reaction temperature maintained between 100–130° the pressure decreased as the reaction proceeded, and one to two hours were required to consume the ethylene oxide used. The addition products are yellow or orange oily materials soluble in water. Aqueous solutions showed good surface-active properties.     

A highly stable and efficient catalyst for direct synthesis of LPG from syngas

Liquefied petroleum gas (LPG) fuel was directly synthesized from syngas over a hybrid catalyst which contained a methanol synthesis catalyst and zeolite. The new hybrid catalyst composed of (Pd–Ca/SiO₂) and β-zeolite, showed a high activity and selectivity for LPG production. X-ray diffraction (XRD) characterization of the catalyst was used to analyze the deactivation of (Pd–Ca/SiO₂)/β-zeolite.     

Evaluation of hydrogen absorption properties of Ti–0.2 mass% Pd alloy in fluoride solutions

The hydrogen absorption properties of Ti–0.2 mass% Pd (Ti–0.2Pd) alloy in 2.0% and 0.2% acidulated phosphate fluoride (APF) and neutral 2.0% NaF solutions (25 °C) has been evaluated by hydrogen thermal desorption analysis. During the early stage of immersion (120 h) in the 2.0% APF solution, the amount of absorbed hydrogen was lower than 500 mass ppm. A thermal desorption of hydrogen primary appearing with a peak at 500–600 °C and a broad desorption ranging from 100 to 400 °C were observed. In the 0.2% APF solution, the amount of absorbed hydrogen saturated at 100–200 mass ppm; the thermal desorption of hydrogen appeared with a single peak at 550 °C. In the 2.0% NaF solution, hydrogen absorption was negligible even after 1000 h of immersion, although corrosion pits were observed. The results of the present study suggest that the hydrogen absorption of Ti–0.2Pd alloy, as compared with commercial pure titanium, is suppressed in fluoride solutions.