Room temperature crystallization by RF plasma

The crystallization of amorphous thin films was achieved by radiofrequency (RF) plasma treatment. Although various amorphous films are crystallized after 2 min or so, the sample temperature is lower than 150 °C without compulsory cooling even when the films are treated for 1 h. This treatment works on amorphous films of various materials, independently of the film preparation method and substrate materials. Sol-gel-derived TiO₂ films were densified and simultaneously crystallized to anatase structure by the plasma treatment and the obtained films indicate almost the same photocatalytic activities as that of thermally crystallized TiO₂ films. Plasma-crystallized sputtered indium tin oxide (ITO) films have a bixbite structure and the resistivity reached to 1.6 × 10^− 4 Ω cm while the crystallization condition was not optimized. Amorphous silicon films with a small mount of crystallites were deposited by sputtering method and were crystallized by the plasma treatment.     

Characterization of sputtered triple layer photoactive coating with a glass-like appearance

Photocatalytic activity of sputtered TiO₂ single layer was investigated. From the results on the optical constants analyses and dark- and photo-conductivity measurements, it is revealed that the photocatalytic activities of TiO₂ films depend on the defect density of the TiO₂ films; the atomic defects act as recombination sites for photo-generated carriers diffusing to the TiO₂ surface. A three-layer system with a layer construction of SnO₂/TiO₂/Si₃N₄/Glass was designed for realizing the glass-like appearance, namely almost the same transmission and reflection spectra in visible wavelength region as those of glass, and its photocatalytic activity was investigated. The experimental results indicate that the interface between TiO₂ and SnO₂ acts as a potential barrier for the carriers photo-generated in the TiO₂ and the photo-generated species pass through the SnO₂ overlayer depending on the SnO₂ film characteristics.     

Improved hydrophilicity of zinc oxide-incorporated layer-by-layer polyelectrolyte film fabricated by dip coating method

ZnO nanoparticles suspended in poly(acrylic acid) (PAA) were deposited onto layer-by-layer (LBL) polyelectrolyte (PET) films fabricated from poly(allylamine hydrochloride) (PAH) and PAA by dip coating method. Effect of etching time and concentration of ZnO suspension on hydrophilicity of the LBL-PET films before and after UV irradiation was examined using water contact angle measurement. 2.0 M PAH/PAA solutions with a dipping speed of 3.0 cm/min provided stable LBL-PET films with thickness sufficient for HCl etching. Glass substrates with the etched LBL-PET film dipped into 0.2 wt.% ZnO suspension exhibited the contact angle of 10° after irradiated by UV for 60 min.     

α-gel prepared in sodium methyl stearoyl taurate/behenyl alcohol/water system-characterization of structural changes with water concentration

In this study, the changes in the structural and physicochemical properties of an α-crystalline phase (often called an "α-gel") were assessed in a sodium methyl stearoyl taurate (SMT)/behenyl alcohol/water system. The α-gels were characterized focusing on the effects of the alcohol/surfactant ratio and water concentration. Water molecules solubilized in the interlayer of the α-crystalline phase resulting in expanded interlayer spacing. Beyond the solubilization limit of 85 %, water molecules were trapped in the matrix of the α-crystalline phase in non-equilibrium (i.e., two phases). Accordingly, different self-diffusion coefficients for the solubilized and trapped water molecules were measured using a Fourier transform pulsed gradient spin echo technique to monitor the 1H NMR spectra. It was concluded that the two self-diffusion coefficients correspond to the water solubilized in the interlayer, i.e., "slow water," and trapped in the matrix of the α-crystalline phase, i.e., "fast water."     

A phenolic antioxidant from the Pacific oyster (Crassostrea gigas) inhibits oxidation of cultured human hepatocytes mediated by diphenyl-1-pyrenylphosphine

3,5-Dihydroxy-4-methoxybenzyl alcohol (DHMBA), an antioxidant isolated from the Pacific oyster (Crassostrea gigas), was studied in a cell-based fluorometric antioxidant assay using human hepatocyte-derived cells (C3A) and diphenyl-1-pyrenylphosphine (DPPP) as a fluorescent probe. In comparison with two hydrophilic antioxidants, DHMBA showed the stronger inhibition of DPPP-mediated fluorescence than chlorogenic acid and l-ascorbic acid: at a concentration of 320 μM of DPPP, the inhibition was 26.4 ± 2.6%, 11.1 ± 1.2%, and 0 ± 2.0% for DHMBA, chlorogenic acid, and l-ascorbic acid, respectively (mean ± SD, n = 4). Their relative oxygen radical absorbance capacities (ORAC) were dissociated with their cell-based antioxidant activities: 1.47 ± 0.40, 4.57 ± 0.30, and 0.53 ± 0.13 μmol TE/μmol for DHMBA, chlorogenic acid, and l-ascorbic acid, respectively (mean ± SD, n = 4). The amphiphilicity of DHMBA was better than chlorogenic acid and l-ascorbic acid might underlie this dissociation. Since the C3A cells are human hepatoma-derived cells, DHMBA might be useful in the prevention and treatment of liver diseases by involving an oxidation process.     

Consideration on the Relationship Between Dielectric Breakdown Voltage and Water Content in Fatty Acid Esters

Mineral oil is commonly used as an electrical insulating oil in transformers because of its relatively high electrical insulating ability and fluidity. Considering the depletion of resources and environmental problems, however, fatty acid esters synthesized from natural plant oils are attracting attention as an environmentally friendly insulating oil. In addition, fatty acid esters such as methyl octanoate, methyl dodecanoate, 2-ethylhexyl octanoate, and 2-ethylhexyl dodecanoate have high fluidity, and also show excellent moisture tolerance against dielectric breakdown compared to mineral oil. In the present study, to clarify the reason for the superior moisture tolerance of fatty acid esters, the status of dissolved water in esters is investigated with IR spectroscopic measurements and density functional theory (DFT) calculations. It is revealed that water molecules in fatty acid esters are trapped by the ester moiety of fatty acid esters. As a result, fatty acid esters have a higher moisture tolerance against dielectric breakdown than mineral oil.     

Development and validation of an HPLC-based screening method to acquire polyhydroxyalkanoate synthase mutants with altered substrate specificity

A rapid and convenient method for the compositional analysis of polyhydroxyalkanoate (PHA) was developed using high-performance liquid chromatography (HPLC) and alkaline sample pretreatment in a 96-well plate format. The reliability of this system was confirmed by the fact that a mutant with a D171G mutation of Aeromonas caviae PHA synthase (PhaC(Ac)), which gained higher reactivity toward 3-hydroxyhexanoate (3HHx), was selected from the D171X mutant library. Together with D171G mutant, several single mutants showing high reactivity toward 3HHx were isolated by the HPLC assay. These new mutants and double mutants combined with an N149S mutation were used to synthesize P(3-hydroxybutyrate-co-3HHx) in Ralstonia eutropha PHB(-)4 from soybean oil as carbon source, achieving higher levels of 3HHx fraction than the wild-type enzyme. Based on these results, the high-throughput screening system will serve as a powerful tool for exploring new and beneficial mutations responsible for regulating copolymer composition of PHA.     

Acceleration of cellulose degradation and shift of product via methanogenic co-culture of a cellulolytic bacterium with a hydrogenotrophic methanogen

Although the effects of syntrophic relationships between bacteria and methanogens have been reported in some environments, those on cellulose decomposition using cellulolytic bacteria from methanogenic reactors have not yet been examined. The effects of syntrophic co-culture on the decomposition of a cellulosic material were investigated in a co-culture of Clostridium clariflavum strain CL-1 and the hydrogenotrophic methanogen Methanothermobacter thermautotrophicus strain ΔH and a single-culture of strain CL-1 under thermophilic conditions. In this study, strain CL-1 was newly isolated as a cellulolytic bacterium from a thermophilic methanogenic reactor used for degrading garbage slurry. The degradation efficiency and cell density of strain CL-1 were 2.9- and 2.7-fold higher in the co-culture than in the single-culture after 60?h of incubation, respectively. Acetate, lactate and ethanol were the primary products in both cultures, and the concentration of propionate was low. The content of acetate to total organic acids plus ethanol was 59.3% in the co-culture. However, the ratio decreased to 24.9% in the single-culture, although acetate was the primary product. Therefore, hydrogen scavenging by the hydrogenotrophic methanogen strain ΔH could shift the metabolic pathway to the acetate production pathway in the co-culture. Increases in the cell density and the consequent acceleration of cellulose degradation in the co-culture would be caused by increases in adenosine 5'-triphosphate (ATP) levels, as the acetate production pathway includes ATP generation. Syntrophic cellulose decomposition by the cellulolytic bacteria and hydrogenotrophic methanogens would be the dominant reaction in the thermophilic methanogenic reactor degrading cellulosic materials.