Substituent effects on thermal and photo‐alignment behavior of poly(ethylene imine)s carrying azobenzene side groups

A new class of liquid‐crystalline poly(ethylene imine)s (PEIs) having four differently substituted (? CN,? C₄H₉,? OCH₃ and? NO₂) azobenzene side‐chain groups attached through alkyl spacer groups were successfully synthesized using a solution polycondensation reaction. The synthesized polymers were characterized using differential scanning calorimetry, polarized optical microscopy and X‐ray diffraction. The photochemical, thermo‐optical and photo‐orientational behavior of the polymers were investigated in detail. Spin‐coated films of PEIs with azobenzene groups having? C₄H₉,? OCH₃ and? NO₂ substituents showed out‐of‐plane molecular orientation on annealing. Except for the PEI with an azobenzene group having ? NO₂ substituent, all polymers exhibited good photoresponsive properties upon irradiation with UV and visible light. Films of PEIs with azobenzene side groups having? CN,? C₄H₉ and? OCH₃ substituents showed reversible alignment behavior from random state to out‐of‐plane and from out‐of‐plane to random state on annealing and on irradiation with UV and non‐polarized visible light. The reversibility of the molecular orientation of PEIs from random state to out‐of‐plane and from out‐of‐plane to random state greatly depended on the substituent attached to the azobenzene side‐chain group. Copyright © 2010 Society of Chemical Industry     

Reforming of Methane with Carbon Dioxide over a Catalyst Consisting of Ruthenium Metal and Cerium Oxide Supported on Mordenite

Reforming of CH₄ with CO₂ proceeds at 400 °C over a catalyst consisting of ruthenium metal and CeO₂ highly dispersed on mordenite. The catalyst, Ru-CeO₂/MZ, is highly active for the reforming of CH₄ under the conditions at which a carbon formation reaction is thermodynamically apt to take place. The reforming selectively forms H₂ and CO. An increase in the weight of the catalyst resulting from carbon deposits was scarcely observed. IR spectra for the catalyst indicate that the reforming proceeds via the formation of the intermediate species such as Ru-CO and Ru-CH_x on the surface of ruthenium. The data of H₂ adsorption support the idea that ruthenium is highly dispersed in Ru-CeO₂/MZ.     

Surface properties of carbon micro-coils oxidized by a low concentration of oxygen gas

Vapor-grown carbon micro-coils were oxidized under a low O₂ flow-rate for introducing oxygen-containing functional groups on the surface. The surface characteristics were then examined. The O1s/C1s intensity ratios of the XPS spectra measured on the surface increased on using the oxidation treatment. The maximum O1s/C1s ratio of 11.4 at.% was obtained under the following conditions: (a) the flow-rate of the mixed gas of O₂+Ar (O₂/Ar=1/10) was 82.5 sccm; (b) the oxidation temperature was 600°C; and (c) the treatment time was 30 min. The maximum O1s/C1s ratio is about 3.5 times that of the source carbon coils. The specific surface area significantly increased due to the oxidation treatment and attained a maximum value of 1050 m² g⁻¹, which is about 10 times that of the source carbon coils. As the specific surface area increased, the surface morphology of the carbon coils became more complicated on a nanometer scale.     

Determination of residual avoparcin in chicken muscle by HPLC with ultraviolet and amperometric detection

An analytical method was developed for determination of residual avoparcin in chicken muscle by measuring alpha- and beta-avoparcin, major components of the pharmaceutical preparation avoparcin, using HPLC with UV and amperometric detectors. The analytical HPLC was run on a Cosmosil 5C18-AR column (4.6 mm x 25 cm) with a gradient formed from A: 2.5% acetic acid, 0.01 mol/L sodium heptane sulfonic acid-acetonitrile (88.5:11.5) (pH 4.0) and B: 2.5% acetic acid-acetonitrile (10:90), using UV and amperometric detection (AMD) with glassy-carbon electrode (+900 mV). Avoparcin was extracted from chicken muscle by homogenization with methanol-0.2 mol/L sulfuric acid (6:4) followed by centrifugation after pH adjustment to 4 with 1 mol/L sodium hydroxide. The supernatant was evaporated to dryness, and the residue was dissolved in water. The aqueous layer was adjusted to pH 4 by adding 1 mol/L sodium hydroxide. Then it was purified on a Sep-Pak tC18 plus ENV cartridge. The cartridge was washed with water, and retained substances were eluted with 50% methanol. The eluate was evaporated to dryness under reduced pressure. The residue was dissolved in water and determined by HPLC. Recoveries of avoparcin spiked in chicken muscle were 73.1-88.1% at levels of 2-10 micrograms/g. The detection limits were 0.5 microgram/g (UV) and 0.2 microgram/g (AMD).     

Lymphatic networks in the periodontal tissue and dental pulp as revealed by histochemical study.

The structural organization and fine distribution of the lymphatic networks in the periodontal tissues (gingiva, periodontal membrane, and alveolar process) and dental pulp of animals and humans were reviewed with special reference to histochemical examination by light and electron microscopy. The distinction between lymphatics and blood vessels was made on cryostat sections of undecalcified and calcified teeth treated with EDTA solution and whole mount preparations of periodontal membranes using 5'-nucleotidase (5'-Nase)-alkaline phosphatase (ALPase) double staining. This staining procedure allowed lymphatic vessels in the periodontal tissue and dental pulp to be differentiated from blood vessels. The specificity and localization of the enzyme reactions were confirmed by comparative histochemical studies of the same specimen with light microscopy and scanning or transmission electron microscopy. Well-developed 5'-Nase-positive lymphatic networks were observed on the tissue sections and whole mount preparations of the gingiva, periodontium, and dental pulp. More lymphatic vessels were seen in the root area of the periodontium than in the cervical area. In the dental pulp, lymphatic vessels were more numerous in the central part than in the peripheral odontoblastic layer. These distributions of the lymphatic capillary networks are discussed in relation to their ability to supply lymph to the teeth.     

A 1.0-V 230-MHz column access embedded DRAM for portable MPEGapplications

This paper describes a 32-Mb embedded DRAM macro fabricated using 0.13-μm triple-well 4-level Cu embedded DRAM technology, which is suitable for portable equipment of MPEG applications. This macro can operate 230-MHz random column access even at 1.0-V power supply condition. The peak power consumption is suppressed to 198 mW in burst operation. The power-down standby mode, which suppresses the leakage current consumption of peripheral circuitry, is also prepared for portable equipment. With the collaboration of array circuit design and the fine Cu metallization technology, macro size of 18.9 mm² and cell efficiency of 51.3% are realized even with dual interface and triple test functions implemented     

Fabrication of 80 mm diameter-sized solid oxide fuel cells using a water-based NiO–YSZ slurry

Solid oxide fuel cells (SOFCs) are very attractive for their high energy conversion efficiency and low emissions. Generally, a supported layer of SOFCs is fabricated by tape casting, using an organic solvent. Recently, a slurry based on water instead of an organic solvent has been sought in order to avoid environmental pollution. In this study, the anode of SOFCs was fabricated by aqueous tape casting, and the electrolyte and the cathode were deposited by screen printing. The I–V characteristics of the cell thus obtained were evaluated. As a result, an 80 mm diameter-sized cell with a power density of 0.33 W/cm² at 800 °C was successfully fabricated by controlling sintering conditions.     

Epitaxial synthesis of poly(p-xylylene)

When poly(p-xylylene) is synthesized from gaseous monomers, it grows epitaxially on substrates. The effects of the substrate and annealing on the epitaxy are examined by growing the polymer on cleavage (001) surfaces of four kinds of alkali halides (NaCl, KCl, KBr and Kl). The polymer crystallizes with its chains oriented along the 〈100〉 and 〈010〉 directions of the substrates and the faster growth planes are parallel to the (001) plane of substrate, i.e., the (010) plane of the α-form crystal and the (100) plane of the β-form. The degree of orientation is the highest on KBr and the lowest on NaCl. The lattice matching requirement is important in the epitaxial synthesis. The observed orientation of the polymer chain on each substrate is compared with the orientation expected from a minimum of interfacial potential energy calculated on the basis of dispersion-repulsive forces between atoms in the polymer and ions in the substrate. The orientational angle of polymer chain on the substrates and the degree of its orientation are qualitatively explained in terms of the processes of monomer deposition, polymerization and crystallization under the directive influence of the substrate.     

Photoresponsive Crown Ethers. Part 11. Azobenzene-Pillared Cylindrical Macrocycle As a Photoresponsive Receptor

A cylindrical ionophore (1) in which two diaza-crown ethers are linked by two azobenzene pillars serves as a photoresponsive host molecule. In alkaline solution containing K⁺, (1) forms a cascade complex with dianionic guest molecules, but photoirradiated (1) which has a shortened cylinder cannot bind the guest molecules so effectively as (1). (1) solubilised in acidic aqueous solution by protonation of four tertiary nitrogens provides a hydrophobic cavity to bind several anionic azo dyes. The association is also suppressed by photoirradiation. The results indicate that parallel array of the azobenzene segments in (1) provides a host cavity and the photoinduced structural change is readily reflected by the association tendency. This is the first example for the photoresponsive inclusion complex.     

Development of an on‐line partial discharge monitoring system for gas insulated substations

This paper describes the results of tests and discussions carried out to develop a system for partial discharge monitoring in GIS. They include the propagation characteristics of partial discharge pulses in each GIS component, as well as the test results obtained using an actual 300‐kV GIS. We also report the results of verification test on the GIS partial discharge monitoring and location system developed by the authors. © 1999 Scripta Technica, Electr Eng Jpn, 129(2): 40–50, 1999