Study on inverse spinel zinc stannate, Zn2SnO4, as transparent conductive films deposited by rf magnetron sputtering

Inverse spinel zinc stannate (Zn₂SnO₄, ZTO) films were deposited onto fused quartz glass substrates heated at 800 °C by rf magnetron sputtering using a ceramic ZTO target (Zn:Sn = 2:1). H₂ flow ratios [H₂/(Ar + H₂)] were controlled from 0 to 30% during the depositions. ZTO films deposited at 800 °C possessed a polycrystalline inverse spinel structure. The lowest resistivity of 1.1 × 10^− 2 Ω cm was obtained for a ZTO film deposited at 20% H₂ flow ratio. The transmittance of the ZTO film was approximately 80% in the visible region.     

Preparation and electrochemical properties of pure lithium cobalt oxide films by electron cyclotron resonance sputtering

Positive Li–Co–O films for all-solid-state thin-film lithium batteries were prepared by electron cyclotron resonance (ECR) sputtering using Li_xCoO₂ targets (x = 1.0, 1.2, 1.7 and 2.0). The Li–Co–O films prepared using the x = 1.0, 1.2 and 1.7 targets contained a Co₃O₄ impurity phase with high-temperature phase LiCoO₂. The film prepared using the x = 2.0 target was found to contain only a pure LiCoO₂ phase by Raman spectrometry and the inductively coupled plasma/atomic emission spectrometry (ICP/AES) method, and a thin-film battery using this film exhibited good electrochemical properties as a result of the improved utilization of the positive film.     

Facile Preparation of an Enzyme‐Immobilized Microreactor using a Cross‐Linking Enzyme Membrane on a Microchannel Surface

The enzyme microreactor has considerable potential for use in biotechnological syntheses and analytical studies. Simplifying the procedure of enzyme immobilization in a microreactor is attractive, and it is achievable by utilizing enzyme immobilization techniques and taking advantage of the characteristics of microfluidics. We previously developed a facile and inexpensive preparation method for an enzyme‐immobilized microreactor. The immobilization of enzymes can be achieved by the formation of an enzyme‐polymeric membrane on the inner wall of the microchannel through cross‐linking polymerization in a laminar flow. However, this method is unsuitable for use in conjunction with electronegative enzymes. Therefore, a novel preparation method using poly‐L ‐lysine [poly(Lys)] as a booster and an adjunct for the effective polymerization of electronegative enzymes was developed in this study. Using aminoacylase as a model for an electronegative enzyme, the reaction conditions for the enzyme‐cross‐linked aggregation were optimized. On the basis of the determined conditions, an acylase‐immobilized tubing microreactor was successfully prepared by cross‐linking polymerization in a concentric laminar flow. The resulting microreactor showed a higher stability against heat and organic solvents compared to those of the free enzyme. The developed method using poly(Lys) was applicable to various enzymes with low isoelectric points, suggesting that this microreactor preparation utilizing a cross‐linked enzyme in a laminar flow could be expanded to microreactors in which a broad range of functional proteins are employed.     

Structure and viscoelastic properties of segmented polyurethane blends

Structure and viscoelastic properties of segmented polyurethanurea (SPU) blends were investigated. The glass transition temperature (T_g) of poly(tetramethylene glycohol) (PTMG) in a soft-segment block of the component SPU increased with decreasing molecular weight of PTMG. The blend samples showed two T_gs of PTMG in the temperature dispersions of the loss modulus (E″) and loss tangent (tan δ). The value of E′ in the leathery region for the blend specimens was trongly affected by the morphology. The blends were considered to have a morphology where PTMG differing in molecular weight was localized. © 1996 John Wiley & Sons, Inc.     

Microbial synthesis and properties of poly(3-hydroxybutyrate-co-4-hydroxybutyrate)

Microbial synthesis of copolymers of [R]-3-hydroxybutyrate (3HB) and 4-hydroxybutyrate (4HB), P(3HB-co-4HB), by Alcaligenes eutrophus, Alcaligenes latus, and Comamonas acidovorans from various carbon sources has been studied. The copolyester compositions varied from 0 to 100 mol% 4HB, depending on the microorganism and the combination of carbon substrates supplied. The thermal and physical properties of compositions with 0–100 mol% 4HB were investigated. The copolyesters represented a wide variety of polymeric materials, from hard crystalline plastic to very elastic rubbers, depending on composition. The copolyester films with high 4HB fractions (64–100 mol% 4HB) exhibited the characteristics of a thermoplastic elastomer, and the tensile strength increased from 17 to 104 MPa as the 4HB fraction increased. The enzymatic degradation of P(3HB-co-4HB) films was studied in an aqueous solution of extracellular polyhydroxybutyrate (PHB) depolymerase from Alcaligenes faecalis or lipase from Rhizopus delemer. The erosion rate of P(3HB-co-4HB) films was strongly dependent on the copolymer composition. In addition, environmental degradation of P(3HB-co-4HB) films in sea water was investigated.     

Spray-dry synthesis of β-Cu1.8Zn0.2V2O7 ceramic fine particles showing giant negative thermal expansion

We used spray-dry method to synthesize fine powder of β-Cu_1.8Zn_0.2V₂O₇ showing large negative thermal expansion (NTE) linearly to temperature over a wide temperature range. The NTE of β-Cu_1.8Zn_0.2V₂O₇ is produced by microstructures consisting of voids and anisotropic thermal deformation of crystal grains in ceramics. By reducing the size of the microstructures that produce NTE, large NTE equivalent to that of bulk was realized, even for ceramic particles of about 2 μm size. Comparison with particles produced using a conventional method demonstrates that the particle size distribution is narrow and that the particles are nearly spherical. This achievement is expected to pave the way to use of NTE materials in micrometer-scale control of thermal expansion.     

Flexible ultraviolet detector with robust ZnO nanoparticle nanoassemblies on catechol-functionalized polysiloxane nanofilms

As a result of the vast Young's moduli difference between an inorganic semiconducting channel and flexible substrates, flexible optoelectronic devices readily lose their functionality through material delamination and local fracturing, which lead to short-circuiting of devices. For this study, we synthesized a catechol-containing polysiloxane (CFPS) adhesive and applied it to ZnO nanoparticle (NP) assembly on plastic substrates for flexible UV detector applications. The 30 nm thick CFPS adhesive can anchor 70 nm thick ZnO NPs strongly through a coordination bond, thereby forming an ultra-stable ZnO NP channel layer. A peeling test of ZnO NP layer was conducted using transparent tape (Scotch®; 3 M Inc.). The ZnO NPs were firmly immobilized, reflecting the outstanding mechanical stability of CFPS adhesives. A UV detector also exhibited stable photo-response performance even after a thousand iterations of bending with 3 mm curvature radii. The result indicates the polycyclosiloxane-based flexible device as promising for wearable detector applications.     

Fractal Structure of Deformed Potato Starch and Its Sorption Characteristics

A deformation of microstructure was attempted on native potato starch and the change in the microstructure was analyzed from the fractal view point. The surface area calculated from the monolayer molecular number was different depending on the molecules used (Ar, N₂, Kr, 1-propanol, and benzene), which showed the surface microstructure was a fractal with the dimension 2.1-2.4. The specific surface area measured using N₂ and benzene was a function of the mean diameter of the material particles, which also showed that the porous structure of the particle was a fractal with the dimension 2.2-3.0. On the other hand, the sorption isotherm of water vapor was independent of particle diameter.     

Theoretical study on vapour phase Beckmann rearrangement of cyclohexanone oxime over a high silica MFI zeolite

We have studied an activation mechanism of cyclohexanone oxime in a cavity of high silica MFI zeolite by using PIO analysis proposed by Fujimoto et al. DFT calculation reveals that the bond length of N–OH becomes longer when water coordinates on oxygen of oxime. The PIO clearly shows out-of-phase interaction between N and O. This out-of-phase interaction is also observed in the PIO of oxime/MFI zeolite cluster model and weakens the N---O bond. Hydrogen bond of Si–OH of nest silanols to oxime is a trigger of vapour phase Beckmann rearrangement.     

Daily peak electric load forecasting using an artificial neural network and an improvement method for reducing the forecasting errors

This paper proposes a forecasting method for shortterm peak electric loads using a 3-layer neural network of locally active units. Each unit in the hidden layer of the neural network is activated only by input vectors in a bounded domain of vector space. This characteristic enables additional learning. Furthermore, it is supposed to provide the network structure with information that helps to improve forecasting accuracy. The neural network is applied to daily peak load forecasting simulations in summer. The results show that the proposed method is superior to a conventional neural network with the backpropagation algorithm. To make the best use of the neural network, an error-oriented method of parameter modification is also examined.