Anhydrous proton conductor consisting of pectin–inorganic composite material

An organic–inorganic proton conductive composite material consisting of a biopolymer was prepared by mixing the pectin, tetraethyl titanate, and imidazole. Although the pectin material without the composite dissolved in water, the pectin–inorganic composite material did not show water solubility. In addition, in the composite material, the pectin and imidazole formed an acid–base structure by an electrostatic interaction, and as a result, these composite materials showed a thermal stability at intermediate temperatures (100–200°C). Furthermore, these composite materials indicated the proton conductivity of 5.6 × 10^?4 S cm^?1 at 180°C under anhydrous conditions. The activation energy of the proton conduction under anhydrous conditions was 0.32–0.22 eV and these values were one order of magnitude higher than that of the typical humidified perfluorinated membrane, such as Nafion^®. The organic–inorganic composite material consisting of a biocomponent may have the potential to be utilized as a novel proton conductor under anhydrous conditions. © 2015 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 42433.     

Preparation of poly(ethylene glycol)-modified poly(amidoamine) dendrimers with a shell of hydrophobic amino acid residues and their function as a nanocontainer

We studied the use of poly(ethylene glycol) (PEG)-modified dendrimers as a nanocapsule with a biocompatible surface. We designed PEG-modified dendrimers having a shell of hydrophobic amino acid residues in the peripheral moiety of the dendrimer to increase their encapsulation ability. Subsequently, l-phenylalanine or γ-benzyl-l-glutamate residues were introduced to all chain ends of the poly(amidoamine) G4 dendrimers. Furthermore, PEG (MW 2000) chains were attached to the amino acid residues. These hydrophobic amino acid residues rendered the PEG-modified dendrimers as more compact. After binding of Rose Bengal (RB) guest molecules to dendrimers, an assay using the Klotz plot showed that the hydrophobic amino acid layer slightly affected the guest site number, but significantly increased intrinsic binding of the dendrimers to guest molecules. The PEG-modified dendrimers with the hydrophobic amino acid layer were better able to retain guest molecules than the dendrimer without the layer: they are therefore useful for drug delivery.     

Applications of microstructures fabricated by proton beam writing to electric-micro filters

Fabrication of high-aspect-ratio microstructures was performed by proton beam writing (PBW) using a microbeam line at Takasaki Ion Accelerators for Advanced Radiation Application (TIARA), JAEA Takasaki, JAPAN. As one of the applications of the high-aspect-ratio structures micro-machined by PBW, we utilized the high-aspect pillars for electric-micro filters of microbes such as Escherichia coli and Yeast based on the dielectrophoretic force. The filter is equipped with high-aspect pillars with a height of ～20 μm and a diameter of ～1 μm on a glass plate. Evaluation of the dielectrophoresis (DEP) device for capturing E. coli and Yeast was made using either observation by optical microscope or photoluminescence (PL) measurements.     

High-performance carbon counter electrode for dye-sensitized solar cells

Here, we reported that a new carbon electrode prepared with an activated carbon was superior to a Pt sputtered electrode as the counter electrode of dye-sensitized solar cells. The photovoltaic performance was largely influenced by the roughness factor of carbon electrode. The open-circuit voltage increased by about 60 mV using the carbon counter electrode compared to the Pt counter electrode because of positive shift of the formal potential for I₃⁻/I⁻ couple.     

Alignment control of liquid crystals in a 1.0‐μm‐pitch spatial light modulator by lattice‐shaped dielectric wall structure

We achieved uniform liquid crystal (LC) alignment in lattice‐shaped dielectric walls 1 μm in pitch; this is a prerequisite when driving the individual pixels of spatial light modulators, facilitating the development of practical electronic holographic displays with a wide field of view. In lattice‐shaped dielectric walls, LC alignment becomes unstable, particularly on the bottom and the walls; the LC directors tend to align parallel to the walls. To overcome this problem, we created lattice‐shaped walls featuring partition plates that allow uniform LC alignment. When the plates confine LCs to small regions exhibiting spatial anisotropy, the LC elastic effect and wall anchoring forces align the LC directors parallel to the long anisotropic axis. We found that pixels 0.5 μm × 1.0 μm in pitch formed if the partition plates were sufficiently thick to allow shielding of electric field leakage.     

Synthesis of zirconia sphere particles based on gelation of sodium alginate

Zirconia sphere particles were synthesized through the gelation process of Na-alginate, and cermet (ZrO₂-Mo) pellets were fabricated under several conditions. In this process, a zirconia slurry was prepared by mixing oxide powders (ZrO₂, Y₂O₃, Er₂O₃, CeO₂), distilled water and Na-alginate, and subsequently dropped into CaCl₂ solution. As a result, zirconia sphere particles coated with a gelled film were synthesized. The slurry density (zirconia content in slurry) of 30-64 wt.% and Na-alginate concentration of a few% were good for gelation for up to 10 wt.% CaCl₂ solution. Sphere particles with smaller diameter were obtained by dropping slurry with a mechanical vibration. The prolongation of the ball milling time for mixture of oxide powders was effective to increase the sintered density of zirconia sphere particles, especially for higher CeO₂ concentration. The dense cermet pellets were fabricated for max. 50% volume ratio of zirconia phase for Mo matrix using zirconia particles covered with Mo powder by a rotating granulation method.     

Carbon Nitride Loaded with an Ultrafine,Monodisperse, Metallic Platinum-Cluster Cocatalyst for the Photocatalytic Hydrogen-Evolution Reaction

For the realization of a next-generation energy society, further improvement in the activity of water-splitting photocatalysts is essential. Platinum (Pt) is predicted to be the most effective cocatalyst for hydrogen evolution from water. However, when the number of active sites is increased by decreasing the particle size, the Pt cocatalyst is easily oxidized and thereby loses its activity. In this study, a method to load ultrafine, monodisperse, metallic Pt nanoclusters (NCs) on graphitic carbon nitride is developed, which is a promising visible-light-driven photocatalyst. In this photocatalyst, a part of the surface of the Pt NCs is protected by sulfur atoms, preventing oxidation. Consequently, the hydrogen-evolution activity per loading weight of Pt cocatalyst is significantly improved, 53 times, compared with that of a Pt-cocatalyst loaded photocatalyst by the conventional method. The developed method is also effective to enhance the overall water-splitting activity of other advanced photocatalysts such as SrTiO₃ and BaLa₄Ti₄O₁₅.     

Minimization of Friction at Various Speeds Using Autonomous Viscosity Control of Nematic Liquid Crystal

To demonstrate the concept of the smart lubrication system using liquid crystal (LC) lubricant proposed by Nakano (Tribol Lett 14:17–24, 2003), the following three types of tests were performed: (1) film thickness measurements in pure rolling contacts, (2) friction coefficient measurements in rolling–sliding contacts, and (3) molecular orientation measurements in stationary cells. In all of these types of tests, a nematic LC [4-pentyl-4′-cyanobiphenyl (5CB)] and a carboxylic acid [hexadecanoic acid (HDA)] were used as the base fluid and the additive, respectively. The results of these tests confirm the following mechanism. First, surface films of the HDA additive that spontaneously adsorb onto contact surfaces induce surface anchoring, which has the effect of making 5CB molecules align themselves perpendicular to the surfaces, competing with the flow alignment of 5CB molecules and inducing an increase in the apparent viscosity of 5CB with decreasing entrainment speed. This increase in the apparent viscosity generates a constant friction coefficient region in the Stribeck curve on the left side of the minimum friction coefficient point, resulting in the minimization of friction at various speeds.     

Fine-tuned,molecular-composite,organosilica membranes for highly efficient propylene/propane separation via suitable pore size

Fine-tuned, molecular-composite, organosilica membranes were fabricated via the co-condensation of organosilica precursors bis(triethoxysilyl)acetylene (BTESA) and bis(triethoxysilyl)benzene (BTESB). Fourier transform infrared and UV–vis spectra confirmed the co-condensation behaviors of BTESA and BTESB. The evolution of the network structure indicated that the incorporated BTESB decreased the membrane pore size, which was determined by a modified gas translation model according to the steric effect of the phenyl groups. The incorporation of BTESB to BTESA finely tuned the membrane structure and endowed the resultant composite membrane with improved separation properties. The BTESAB 9:1 membrane (molar ratio of BTESA/BTESB was 9:1) exhibited high C₃H₆ permeance at 4.5 × 10⁻⁸ mol m⁻² s⁻¹ Pa⁻¹ and a C₃H₆/C₃H₈ permeance ratio of 33 at 50°C. One of the most important developments of this study involved clearly defining the relationship between membrane pore size and C₃H₆/C₃H₈ separation performance for organosilica membranes in single and binary separation systems.