New type of pressurized cultivation method providing oxygen for piezotolerant yeast

For efficient oxygen supply to pressurized culture, we developed a method using a highly pressurized membrane reactor with an air-saturated medium circulation system. The new method increased the cell growth of aerobic yeast approximately 20 folds larger than that in the case of using a conventional method.     

New approach for synthesis of activated carbon from bamboo

Unconventional pretreatment, that is, delignification and the addition of guanidine phosphate, was performed for the synthesis of activated carbon having a high specific surface area from bamboo by physical activation. The values of the specific surface area, total pore volume, and average pore size depended on the amount of added guanidine phosphate and the CO₂ activation time. The amount of the added guanidine phosphate under the optimum conditions for the highest specific surface area was much lower than that of the phosphorous acid chemical activator under conventional conditions. The N₂ adsorption isotherms of all the samples were type I, which means that micropores were dominant. The pore sizes of the samples in this study were similar to that of the physically-activated carbon. Therefore, the activation process was presumed to be essentially not chemical, but physical. The relation between the yield and the specific surface area improved with the addition of guanidine phosphate. The reason for the improvement may be the change in the reactivity of the carbon material generated during the heating process. The maximum specific surface area was ca. 2000 m² g^?1, which is a high value for a physically-activated carbon.     

Electrical properties of diphenyldiacetylene annealed under elevated pressure

A unique class of conjugated compounds composed of the derivative of condensed polycyclic aromatic compound with the phenyl group and diphenyldiacetylene oligomer was synthesized by annealing of diphenyldiacetylene under elevated pressure. The effect of annealing pressure on the conductivity of the compounds was studied. The total conductivity of the compound decreased with a decrease of frequency, approaching a constant value (dc conductivity: C_dc). The dc conductivity of the compound increased from below 10^?15 to 10 S cm^?1 with increasing annealing pressure. The dc conductivity of the oligomer was below 10^?15 S cm^?1 and that of the derivative increased from 10^?8 to 10 S cm^?1 with decreasing H/C (H/C:0.45–0.04). The conduction of the conjugated compound was electronic. The temperature coefficient of those dc conductivities was positive, with an approximately linear relation between In (C_dcT^0.5) and (1/T)^0.25, where T is the temperature. The ac conductivities C_ac were proportional to temperature and frequency f and had the following equation C_ac = Tf^S, S = 0.67–0.75. These results showed that the conduction mechanism can be explained by the hopping in a manifold of states at the Fermi level. © 1994 John Wiley & Sons, Inc.     

Crystallization of nylon 6–clay hybrid by annealing under elevated pressure

Nylon 6–clay hybrid (NCH) is a molecular composite of nylon 6 and uniformly dispersed silicate layers of montmorillonite. We found that the phase with the high melting temperature (HMT phase) in the NCH annealed under elevated pressure. The melting temperature of the HMT phase was 240°C. Nylon 6 annealed under elevated pressure did not have the HMT phase. Thus, the presence of the HMT phase was characteristic of the NCH. The relative heat of fusion of the HMT phase (heat of fusion of HMT phase/heat of fusion in the pressure annealed NCH) increased with increase in pressure. High-pressure differential thermal analysis (DTA) measurement revealed that the temperature, at which the relative heat of fusion showed a maximum value, was below about 20°C of the melting temperature of the original NCH under elevated presssure. It was considered that the nylon 6 crystallite near the melting temperature and the molecular mobility under elevated pressure were necessary to the appearance to the HMT phase. © 1994 John Wiley & Sons, Inc.     

Structural relationship between thermomechanical history and strength of polymeric solids

Ultimate properties in polymeric solids strongly depend on thermomechanical history. We have shown that the polymer structure which depends on thermomechanical history can be quantitatively described by the relative amounts of enthalpy and entropy. The excess enthalpy decreases upon annealing and increases under the tensile stress. The increase in excess enthalpy reduces the relaxation time; thus a local brittle-to-ductile transition may be induced by stress concentration. It follows that in a well-annealed material, this transition is more difficult to induce. Effects of molecular weight and orientation are also discussed in terms of dissipation of strain energy as the condition required for the strength of polymeric solids.     

Analysis of non-linear stress relaxation in polymeric glasses

Non-linear stress relaxation data were obtained for polycarbonate and polystyrene as a function of temperature, strain magnitude and thermal history. Data were analyzed according to the previously proposed free volume model to account for the shift of relaxation times with strain and thermal history. The result of the analysis is shown to be in close agreement with the tensile stress-strain data. The yield phenomenon is analyzed as a rate dependent strain-induced glass to rubber transition.     

Preparation of screen-printed YBCO thick films on an alumina substrate under flowing argon

Y-Ba-Cu-O (YBCO) thick films of 10–15 μm thickness were prepared on bare alumina substrates by the screen-printing technique. The films, which were heated at 850–900 °C in argon atmosphere and then exposed to oxygen, showed zero resistance at 79–84 K.     

Fabrication of colorless organic materials exhibiting white luminescence using normal and excited-state intramolecular proton transfer processes

Organic, white luminescent materials were fabricated using a mixture of proton-transfer and nonproton-transfer fluorophores. 2'-Methoxy and 2'-hydroxy derivatives of 2-phenylimidazo[1,2-a]pyridine (PIP) have similar UV-absorption properties; however, they exhibit mechanistically different luminescence respectively ascribable to the normal (～420 nm) and excited-state intramolecular proton transfer processes (～530 nm) in the solid state. UV-irradiation of mixed solids excites both components concurrently and results in efficient white luminescence composed of two independent emissions without involving energy transfer process. White luminescent solids are easily transformed into vapor-deposited films under mild conditions, and a colorless and transparent thin film by dissolving in PMMA.     

Thermoreversible behavior of κ-carrageenan and its apatite-forming ability in simulated body fluid

Osteoconductive materials with self-setting ability have received much attention because their properties allow developing injectable materials for bone defects. Thermosensitive hydrogel with ability of bone-like apatite formation in a body environment is a candidate of injectable bone fillers with osteoconductivity because the apatite formation on materials is an essential to show osteoconduction. The present study focused on the development of a thermosensitive hydrogel through modifications of the sulphonic groups of the polysaccharide, κ-carrageenan, with potassium chloride (KCl) and calcium chloride (CaCl₂). We found that the gelation temperature of κ-carrageenan solutions increased with increasing amounts of K⁺ ions. Apatite formation was observed on the gel after exposure to simulated body fluid for 0.5 day when the gel was prepared with a molar ratio of Ca²⁺/sulfonic groups = 1.5. These results indicate that a thermosensitive κ-carrageenan hydrogel with apatite-forming ability was obtained through the incorporation of K⁺ and Ca²⁺ ions into the solution.     

Absorption spectra and tautomerism of aminonaphthazarins

2-n-Butylaminonaphthazarin (2) absorbs at 499 and 532 nm in ethanol but at 539 and 577 nm in alkali solution, while 2, 6-bis(n-butylamino)naphthazarin (3) absorbs at 461, 500 and 540 nm in ethanol but at 511 and 545 nm in alkali solution, with only a small bathochromic shift of 5 nm. The absorption curve of 3 was changed by addition of alkali and the λD_max at around 461 nm completely disappeared. In the case of 2-bromo-3, 6-bis(n-butylamino)naphthazarin (4), tautomerism between the 1, 4-quinone and 1, 5-quinone forms was observed and the isosbestic point was observed at 480 nm. Dye 2 easily deprotonated to give the 1, 4-dianion, but dyes 3 and 4 existed as tautomeric mixtures in solution and shifted to 1, 5-quinone forms in alkali solution.