Xylooligosaccharide fermentation with Leuconostoc lactis

Strains of Leuconostoc lactis SHO-47 and Le. lactis SHO-54, producing the clinically useful enzyme NAD-specific 6-phosphoglucanate dehydrogenase, were cultivated with a hydrolyzed birch wood xylan as the unique carbon source to produce D-lactic acid for poly(D-lactic acid). In addition to the strains SHO-47 and SHO-54, Lactococcus lactis IO-1, well known as a good xylose-utilizing lactic acid bacterium, was used as a control to confirm the extent of hemicellulose hydrolysis. The fermentation time for lactic acid of strains SHO-47 and SHO-54 was 12 h, and produced respectively 2.3 and 2.2 g/l lactic acid from 8.5 g/l hydrolyzed xylan, whereas the fermentation time of strain IO-1 was 21 h, and produced 1.3 g/l lactic acid. Xylooligosaccharides from xylobiose to xylohexose were utilized more rapidly than xylose in the cultures of strains SHO-47 and SHO-54. However, xylose concentration increased temporarily and then decreased in the culture of strain IO-1. On the other hand, xylooligosaccharides larger than xyloheptaose were not utilized by these three strains. The xylosidase activities of SHO-47, SHO-54, and IO-1 were induced by xylose or a mixture of xylobiose and xylotriose. The xylosidases of these three strains were localized in their cytoplasm.     

Research on corrugated multi‐louvered fins under dehumidification

To enhance automotive evaporator wet‐fin performances, the main task is to promote the draining of condensed water. An accurate and convenient apparatus estimating the fin performances has been developed. Through the measurement of corrugated multi‐louvered fin performances and the visualization of condensed water draining by this apparatus, it was clarified that fin geometries, surface coating, and evaporator installation strongly contributed to the efficiency of draining and fin performances. © 2001 Scripta Technica, Heat Trans Asian Res, 30(5): 383–393, 2001     

Molecular dynamics study on the cluster structure of the 2‐D LJ fluid and water

A molecular dynamics simulation has been performed for a two‐dimensional Lennard–Jones (12‐6) fluid. A saturated liquid at low temperature, compressed liquid, and fluid at supercritical temperatures with various densities were analyzed. Number of bonds per molecule, lifetime of bonds, connectivity of molecules to form clusters, stability of clusters, and their responses to temperature and density are compared with those of a hydrogen bond in water. © 2000 Scripta Technica, Heat Trans Asian Res, 29(3): 218–232, 2000     

Electrolyte properties of 1-alkyl-2,3,5-trimethylpyrazolium cation-based room-temperature ionic liquids for lithium secondary batteries

The physicochemical and electrochemical properties of three 1-alkyl-2,3,5-trimethylpyrazolium cation-based room-temperature ionic liquids with various alkyl chain lengths were investigated. The temperature dependences of density, viscosity, and ionic conductivity were obtained by precise measurements. Electrolyte properties of these room-temperature ionic liquids were also examined from the viewpoint of their uses in lithium secondary batteries ([LiCoO₂ positive electrode|electrolyte|lithium metal negative electrode]). It was found that the alkyl chain length affects the charge–discharge performances of cells.     

Thermophysical properties of (U,Y)O2

We prepared polycrystalline pellets of (U,Y)O₂, containing YO_1.5 up to 11 mol.%. We performed indentation tests on the pellets, and evaluated the Young’s modulus and hardness. We measured the heat capacity and the thermal diffusivity, and evaluated the thermal conductivity. We succeeded in evaluating the effect of Y content on the thermophysical properties of (U,Y)O₂. We revealed that the Young’s modulus, hardness, and thermal conductivity of (U,Y)O₂ decreased with increasing the Y content.     

Gigahertz-band high-gain GaAs monolithic amplifiers using parallelfeedback technique

A high-grain multistage amplifier design technique is described. As countermeasures against FET drawbacks, the drain conductance dispersion was modeled and the DC parallel feedback was applied against process variations. Based on these and further feedback techniques, a limiting amplifier and a gain-controllable amplifier for satellite communication systems were designed and fabricated utilizing an 0.8 μm gate-length ion-implanted GaAs MESFET process. Moreover, their packages were developed considering stability conditions. A 45 dB 0.1-3.5 GHz limiting amplifier and a 22-38 dB 0.1-2.5 GHz gain-controllable amplifier were developed     

Limiting current density in bis(trifluoromethylsulfonyl)amide-based ionic liquid for lithium batteries

The physicochemical and electrochemical properties of the binary ionic liquid (IL), lithium bis(trifluoromethylsulfonyl)amide (LiTFSA) dissolved in N,N-diethyl-N-methyl-N-(2-methoxyethyl)ammonium bis(trifluoromethylsulfonyl)amide (DEMETFSA), were investigated. The ionic conductivity of the binary IL decreased with an increase in LiTFSA concentration. The self-diffusion coefficients of Li⁺, DEME⁺, and TFSA⁻ dissolved in the IL were measured by using the pulsed-field-gradient spin-echo (PGSE) NMR method. The self-diffusion coefficient of each ionic species was also found to decrease with increasing concentration of LiTFSA. The limiting current density in the IL electrolyte was evaluated by chronoamperometry using symmetric Li|IL|Li cell. The results suggest that the diffusion process of Li(I) in the IL dominates the limiting current density in the cell. The highest limiting current density is achieved at a concentration of 0.64 mol dm⁻³ of LiTFSA.     

Adsorption of trypsin onto poly(2-hydroxyethyl methacrylate)/polystyrene composite microspheres and its enzymatic activity

Poly(2-hydroxyethyl methacrylate)/polystyrene (PHEMA/PS) composite microspheres were produced by emulsifier-free seeded emulsion polymerization for styrene in the presence of PHEMA seed particles. Effects of the surface characteristics of the PHEMA/PS composite microspheres on the adsorption immobilization of trypsin and on its enzymatic activity were discussed. Above 5 mol% of HEMA content, trypsin molecules adsorbed had high activity, 65–100% of the activity of free trypsin. The excellence of the composite microspheres as a carrier for trypsin seems to be closely related with the surface heterogeneity consisting of both hydrophilic and hydrophobic parts.     

Direct imaging of molecular chains in a poly(p-xylylene) single crystal

Individual chains comprising a β-form poly(p-xylylene) (PPX) single crystal were resolved with a high resolution electron microscope (JEM-500). In a polymer crystal the important limiting factor for resolution is radiation damage. The total end point dose of a PPX crystal is about 0.5 coulomb cm^?2 for 500 kV electron irradiation which is more than 20 times greater than that for a polyethylene crystal. The high resolution image obtained was processed by optical filtering to reduce noise due to the granularity of film. The processed image, which corresponds to the ab-plane projection of polymer chains, shows clearly the mutual arrangement of each molecule in the crystal. This high resolution image is sufficient to provide a starting point for determining the unknown crystal structure of the β-modification of PPX.     

The effects of oxygen diffusion on the surface photooxidation of polystyrene

This paper further illustrates the applicability of multiple internal reflectance infrared spectroscopy to the analysis of near-surface photooxidation. The results are compared with transmission infrared spectra to evaluate compositional gradients resulting from photooxidation and the influence of oxygen diffusion. The sample was a solvent-cast film of atactic, narrow distribution polystyrene, M_w of 100,000, that had been drawn to a ratio of 3.0 at 110°C by solid state coextrusion. Irradiation of these thin films, ～25μm thickness, was performed on exposure to air at 35°C for periods of up to 6 h using a mercury source emitting at 254 nm. On photooxidation, a board peak appears at 3200–3500 cm^?1, attributable to hydroperoxide formation. The most dramatic increase in the infrared spectra is found for a carbonyl band at 1730 cm^?1. It appears to result from an aromatic acid group since it is shifted to 1660 cm^?1 on immersion of the oxidized polystyrene films in aqueous ammonium hydroxide. It is confirmed that the photooxidation of polystyrene occurs preferentially at the surface and that this reaction rate is greatly reduced in the drawn polystyrene film.