13.3‐inch 8k4k 664‐ppi foldable OLED display using crystalline oxide semiconductor FETs

A prototype 13.3‐inch 8k4k 664‐ppi high‐resolution foldable organic light emitting diode display is constructed. C‐axis aligned a‐b‐plane‐anchored crystal In–Ga–Zn oxide field effect transistors designed using a 1.5‐µm rule process are used in the backplane. Each pixel circuit has three transistors and one capacitor, and an external circuit is used to correct pixel current.     

Reaction mechanism of coal hydrogenation: 2. Three rings solvent system

Taiheiyo coal was hydrogenated in phenanthrene, 9,10-dihydrophenanthrene, 1,2,3,4,5,6,7,8-octahydrophenanthrene and perhydrophenanthrene under 10 MPa (initial pressure) of hydrogen or nitrogen with or without stabilized nickel as catalyst at 400 °C for 15 min. Preasphaltene, asphaltene and oil conversions and the conversion of solvents were measured, and the amounts of hydrogen absorbed by coal from molecular hydrogen and from donor solvent were calculated. The main route of reaction appears to be the direct hydrogenation of coal by molecular hydrogen and the contribution of hydrogenation via the solvent was greater than in the case of the two rings solvent system.     

Sex Pheromone of the Persimmon Fruit Moth, Stathmopoda masinissa: Identification and Laboratory Bioassay of (4E, 6Z)-4,6-Hexadecadien-1-ol Derivatives

Three electroantennogram (EAG)-active components were detected by gas chromatography coupled to an electroantennographic detector (GC–EAD) analysis of a hexane extract of the pheromone glands of the persimmon fruit moth, Stathmopoda masinissa. These compounds were identified as (4E,6Z)-4,6-hexadecadienal (E4,Z6-16:Ald) and the corresponding acetate (E4,Z6-16: OAc) and alcohol (E4,Z6-16:OH) by mass spectral, GC retention time (RT), and microchemical test data. The characteristic base peak of the aldehyde at m/z 84 provided a crucial piece of information suggesting the possibility of a 4,6-diene structure. The (4E,6Z)-isomer elicited the strongest EAG responses among the four geometrical isomers of each synthetic 4,6-hexadecadienyl compound. In a laboratory bioassay, only E4,Z6-16:OAc elicited male moth behavioral activity significantly different from the control; the activity of the acetate was not affected by addition of the aldehyde and alcohol. A preliminary field trial confirmed that E4,Z6-16:OAc as a single component attracted male moths. The possible roles of E4,Z6-16:Ald and E4,Z6-16:OH as components of lures for field use remain to be determined.     

Microstructural and Thermoelectric Characteristics of Zinc Oxide-Based Thermoelectric Materials Fabricated Using a Spark Plasma Sintering Process

M-doped zinc oxide (ZnO) (M=Al and/or Ni) thermoelectric materials were fully densified at a temperature lower than 1000°C using a spark plasma sintering technique and their microstructural evolution and thermoelectric characteristics were investigated. The addition of Al₂O₃ reduced the surface evaporation of pure ZnO and suppressed grain growth by the formation of a secondary phase. The addition of NiO promoted the formation of a solid solution with the ZnO crystal structure and caused severe grain growth. The co-addition of Al₂O₃ and NiO produced a homogeneous microstructure with a good grain boundary distribution. The microstructural characteristics induced by the co-addition of Al₂O₃ and NiO have a major role in increasing the electrical conductivity and decreasing the thermal conductivity, resulting from an increase in carrier concentration and the phonon scattering effect, respectively, and therefore improving the thermoelectric properties. The ZnO specimen, which was sintered at 1000°C with the co-addition of Al₂O₃ and NiO, exhibited a ZT value of 0.6 × 10⁻³ K⁻¹, electrical conductivity of 1.7 × 10⁻⁴Ω⁻¹·m⁻¹, the thermal conductivity of 5.16 W·(m·K)⁻¹, and Seebeck coefficient of −425.4 μV/K at 900°C. The ZT value obtained respects the 30% increase compared with the previously reported value, 0.4 × 10⁻³ K⁻¹, in the literature.     

Coking reaction in hydrogenation

Asphaltene prepared from a Japanese coal (Akabira, 81.2 wt% C) and coal tar pitch were heat treated under nitrogen or hydrogen. Under nitrogen the initial thermal decomposition produced radicals which abstracted hydrogen from other molecules to stabilize and to produce smaller molecules and gas. The molecules from which hydrogen was abstracted as well as other radicals polycondensed to produce heavier solvent-insoluble fractions. Under hydrogen the radicals were stabilized by hydrogen gas to produce smaller molecules avoiding the production of a heavier fraction. The higher the hydrogen pressure, the smaller was the yield of heavier fraction and the larger the yield of lighter fraction. Higher temperature accelerated the production of the heavier fraction. Donor solvents could reduce the production of the heavier fraction.     

The Role of Intramolecular Quenching in the Catalytic Fading of Dye Mixtures

The catalytic fading of dye mixtures has been investigated, and the influence of a nickel sulphonate group, an intramolecular singlet oxygen quencher, was examined. Dyes containing the quenching group showed improved resistance to catalytic fading in solution and in the solid state.     

Studies on selective adsorption resins. XXI. Preparation and properties of macroreticular chelating ion exchange resins containing phosphoric acid groups

Macroreticular cation exchange resins containing phosphoric acid groups (RGP) were prepared by the reaction of glycidyl methacrylate–divinylbenzene copolymer [or poly(glycidyl methacrylate)]beads (RG) with phosphoric acid or phosphorous oxychloride, and the adsorption behavior of metal ions on the RGP was investigated. The phosphorylation of the polymer beads could be effectively carried out by treatment of the polymer beads with 85% phosphoric acid at 80°C for 3 h. The RGP obtained from glycidyl methacrylate–divinylbenzene (2 mol %) copolymer beads showed high cation exchange capacity, salt splitting capacity, and adsorption capacity for Cu²⁺, Zn²⁺, Cd²⁺, Ca²⁺, and Ag⁺. On the other hand, the RGP obtained from poly(glycidyl methacrylate)beads had high adsorption capacity for Al³⁺, Fe³⁺, and UO₂²⁺. The RGP prepared by treating the RG with phosphoric acid had a higher selective adsorption for Li⁺ than for Na⁺.     

Electrodeposition of metallic molybdenum films in ZnCl2-NaCl-KCl-MoCl3 systems at 250 °C

Molybdenum metal film has been electrodeposited in ZnCl₂-NaCl-KCl (0.60:0.20:0.20, in mole fraction) melt containing MoCl₃ at 250 °C. In this melt, a dense film was obtained by potentiostatic electrolysis at 0.15 V versus Zn(II)/Zn for 3 h. However, the film had a thickness of smaller than 0.5 μm and was not adhesive. On the other hand, addition of 4 mol% of KF to the melt led to larger cathodic current in cyclic voltammogram, and gave a dense, adhesive and thicker metal film of ca. 3 μm thickness in the same electrolysis condition as above. The present process is promising as a new method for molybdenum coating at low temperatures.     

Pressure and temperature effects on the hydrogenation of coal-derived asphaltene

Pressure and temperature effects on hydrogenation reactions were examined using coal-derived asphaltene at 390,420 and 450 °C, under 3 and 10 MPa of hydrogen partial pressure. Higher conversion was obtained at higher reaction temperatures. Benzene-insoluble material (Bl) was formed at higher temperatures especially at low hydrogen pressure, this Bl being one-third of the reaction product at 450 °C. From structural analysis of unreacted asphaltenes and product oils, at 390 °C, it was concluded that smaller molecular components convert to oil initially and the larger molecules remain as unreacted asphaltene. Under higher hydrogen pressure for all temperatures carbon aromaticity (f_a) and number of aromatic ring per structural unit (R_aus) in unreacted asphaltenes were lower than those under lower hydrogen pressure suggesting that hydrogenation of the aromatic nucleus was promoted by higher pressure. At lower hydrogen pressure, R_aus for asphaltenes at higher temperature is larger than that at lower temperature. This suggests that at lower hydrogen pressure, dehydrogenation or condensation reactions occur more easily. A large effect at higher hydrogen pressure was a reduction in the extent of condensation reactions. Higher reaction temperatures contribute to splitting of bridged linkages so reducing molecular size and degree of aromatization.     

Effect of Chemical Composition on the Sinterability of Ultrafine Sic Powders

Ultrafine β-SiC powders with an average particle size of 0.01 to 0.06 μm were produced by CVD methods. When these powders contained enough carbon to remove impurity oxygen, sintered bodies with a relative density >95% were uchieved at 2050°C in the presence of 1 wt% boron. The Vickers microhardness reached 21 to 25 GPa at a density of ∼95% .