Characterization and hydrogen sorption behaviors of FeNiCr-carbon composites derived from Fe,Ni and Cr-containing polyacrylonitrile fibers prepared by electrospinning method

In order to enhance hydrogen storage capacity of carbonaceous materials through metal modification, FeNiCr-carbon composites were prepared by calcination of Fe, Ni and Cr-containing polyacrylonitrile (PAN) fibers fabricated by electrospinning method. Fe (III), Ni (II) and Cr (III) acetylacetonates (M (acac)_n) were selected as metal sources. Increase of specific surface area and formation of micropores were observed on heat decomposition of M (acac)_n particularly through introduction of steam. Maximal hydrogen content, 1.62 mass%, was obtained at 77 K under 0.8 MPa of hydrogen for a FeNiCr-carbon composite, which contained about 15.5 mass% of metals and had specific surface area of 501 m² g^?1. The hydrogen content exceeded the hydrogen physisorption limit, 2.34 mass% per 1000 m² g^?1, which was calculated on the basis of the commensurate–incommensurate transition with an enhancing factor ρ of 1.126. After hydrogenation at 653 K, no hydrogen desorption peaks were observed for FeNiCr powders derived from M (acac)_n, and one peak at 828 K for a carbonaceous sample prepared from unmodified PAN fibers. From the most promising FeNiCr-carbon composite, another peak was recorded at 752 K in addition to the peak at 828 K. The former would be originated from hydrogen on novel sorption sites additionally created on the composite formation.     

Organofunctionalized catalyst surfaces highly active and selective for carbon–carbon bond-forming reactions

This article illustrates two types of organofunctionalized heterogeneous catalysts for variety of organic carbon–carbon bond-forming reactions, summarizing our previous reports and also presenting new data. Organic amines with an alkoxysilane moiety were immobilized on inorganic silica-alumina surfaces (SA-NR₂) by simple silane-coupling reactions between the silica-alumina surface (SA) and the alkoxysilane. This SA-NR₂ acted as acid–base bifunctional heterogeneous catalysts for carbon–carbon bond-forming reactions, such as cyano-ethoxycarbonylation, Michael reaction of nitriles, and nitro-aldol reaction. These reactions did not occur with either SA or homogeneous amine compounds. In addition, the mixture of SA and homogeneous amine showed low catalytic activity due to undesirable acid–base neutralization reaction. Achiral organic silane-coupling reagents with a variety of functional groups were also immobilized on a SiO₂ surface that had been immobilized with chiral bis(oxazoline) (BOX), to which Cu ions were coordinated to make chiral Cu–BOX complexes on the SiO₂ surface. The SiO₂-supported Cu–BOX complex catalyst functionalized with achiral 3-methacryloxypropyltrimethoxysilane dramatically increased enantioselectivity in the asymmetric Diels–Alder reaction of cyclopentadiene and 3-acryloyl-2-oxazolidinone. The organofunctionalized catalysts showed much better performances for the C–C bond-forming reactions compared to the corresponding homogeneous systems. The heterogeneous catalysts thus obtained were characterized by solid-state ¹³C and ²⁹Si MAS NMR, FT-IR, UV/vis, XAFS, ESR, XRF, and elemental analysis.     

Phthalocyanine molecular nanowires that were prepared using porous alumina as a template: Development in the sample preparation procedure to evaluate electronic properties

We have proposed the synthesis of organic molecular nanowires using porous alumina as a template. We also proposed the use of a magnetic field to control the molecular packing structure in the nanowires. In this paper, we developed the method to evaluate the electronic properties of the nanowire of a phthalocyanine derivative that was synthesized using porous alumina as a template. The developed method facilitates the study in the organic molecular nanowires that were synthesized using templates and helps their use in future electronic devices.     

Depression of melting point of eutectic metal alloy by the interaction with polyacrylates in metal-polymer composites

The composites of polyacrylates and eutectic metal alloy composed by Bi, In, and Sn were prepared by mixing the metal and polymer above the melting point of the metal alloy (80 °C) with a homogenizer. Two melting peaks, which were assigned as the melting peak of the original metal alloy and that of the interfacial phase of the metal alloy interacting with polyacrylates (70 °C) by differential scanning calorimetry. Metal particles with the diameter of about 100 nm which were stabilized by the interfacial interaction with polyacrylates were observed by transmission electron microscopy. The melting peak at 70 °C was assigned as the melting peak of these small particles.     

Criteria for versatile GaN MOVPE tool:high growth rate GaN by atmospheric pressure growth

Growth rate has a direct impact on the productivity of nitride LED production.Atmospheric pressure growth of GaN with a growth rate as high as 10μm/h and also Al_0.1Ga_0.9N growth of 1μm/h by using 4 inch by 11 production scale MOVPE are described.XRD of（002） and（102） direction was 200 arcsec and 250 arcsec, respectively.Impact of the growth rate on productivity is discussed.     

Bi-Cu film deposition in aqueous solutions

The relatively uniform bismuth-copper film was electrodeposited between −15 and −20 mV in the sulfate electrolyte containing 4 mmol/L bismuth ion and 2 mmol/L copper ion. Only copper was electrodeposited at −5 mV. The dendritic bismuth-copper film was electrodeposited under −20 mV. The cathodic current became constant between −20 and −400 mV. Therefore, bismuth-copper electrodeposition changes from charge transfer controlling to diffusion controlling at −20 mV. On the other hand, the uniform bismuth-copper film was electrodeposited between −5 and −35 mV in the methanesulfonate electrolyte containing 4 mmol/L bismuth ion and 2 mmol/L copper ion. The dendritic bismuth-copper film was electrodeposited under −35 mV. The potential region for good electrodepositon in methanesulfonate electrolyte is wider than that in sulfate electrolyte. Therefore, it is easy to control electrodeposition conditions by using methanesulfonate electrolyte.     

Simplified method for determining cadmium concentrations in rice foliage and soil by using a biosensor kit with immunochromatography

BACKGROUND: The behavior of cadmium in ecosystems needs to be monitored because of the human toxicity of this heavy metal. The need recently arose for a simple and quick on‐site test for trace levels of Cd in food and environmental samples. In response, an immunochromatographic assay kit for detecting Cd was manufactured by Kansai Electric Power Co. of Japan. This kit uses the antigen–antibody complex reaction between the Cd–EDTA complex and an anti‐Cd–EDTA antibody and shows the results in terms of the degree of color developed on a test paper. We previously reported the successful use of this kit to determine Cd concentrations in brown rice. Here, we applied the kit to the determination of Cd concentrations in rice foliage and soil. RESULTS: Cadmium in rice foliage was not extracted successfully by the method used for brown rice. However, it was successfully extracted by 0.1 mol L^?1 HCl solution at a rice foliage:HCl ratio of 1:20, and coexisting metals were removed sufficiently by the column treatment. The Cd concentrations determined by immunochromatographic assay were well correlated with the values obtained by acid decomposition and inductively coupled plasma mass spectrometry. The 0.1 mol L^?1 HCl‐extractable Cd concentration in soil was also determined successfully with the kit. CONCLUSION: Approximate Cd concentrations in rice plants and 0.1 mol L^?1 HCl‐extractable Cd concentrations in soil can be monitored easily and quickly by this method at locations where facilities for acid digestion and precision analysis are not available. Copyright © 2009 Society of Chemical Industry