Materials for global carbon dioxide recycling

CO₂ emissions, which induce global warming, increase with the development of economic activity. It is impossible to decrease the CO₂ emissions by suppression of the economic activity. Global CO₂ recycling can solve this problem. The global CO₂ recycling consists of three district: The electricity is generated by solar cells on deserts. At desert coasts, the electricity is used for H₂ production by seawater electrolysis and H₂ is used for CH₄ production by the reaction with CO₂. CH₄ which is the main component of liquefied natural gas is liquefied and transported to energy consuming districts where CO₂ is recovered, liquefied and transported to the desert coasts. A CO₂ recycling plant for substantiation of our idea has been built on the roof of the Institute for Materials Research in 1996. Key materials necessary for the global CO₂ recycling are the anode and cathode for seawater electrolysis and the catalyst for CO₂ conversion. All of them have been tailored by us. They have very high activity and selectivity for necessary reactions in addition to excellent durability. A pilot plant consisting of minimum units in an industrial scale is going to be built in three years.     

Morphological characteristics of flood refugia of cobble-bed vegetation

Periodic flooding alters riverine vegetation community composition; moderate flood disturbance maintains communities at an early seral stage, whereas severe floods may remove entire communities. After disturbance, plants may recolonize riverbeds from refugia.Here, we investigated the morphological characteristics of refugia where riverine plants survived large floods. At three sites, plant communities growing on cobble-bars were surveyed, and the hydraulic characteristics of each site were analyzed. The populations of an indicator plant, Anaphalis margaritacea sub-species yedoensis (Franch. et Savat.) were assessed after major floods in 2004 and 2009. At each survey, the particle size and bed composition were measured, and the critical shear-stress required to move particles at each site was calculated. A one-dimensional flow and the average and local shear-stress at ten different discharges, including that of the largest flood were calculated. The results demonstrate that the A. margaritacea community is maintained at locations where the local shear-stress at peak discharge in large-floods does not exceed a critical value. These conditions were achieved in locations with particular morphological characteristics, where the river is not constrained by levees and is restricted by a downstream narrow-pass; in this reach river width increases with discharge thus limiting the increase in water depth with increasing discharge and allowing the establishment of refugia where plant species may survive large floods.Flooding and reestablishment from refugia maintain a characteristic riverbed community in equilibrium.     

粉末冶金结构零件材料的泊松比

研究了粉末冶金机械零件使用的烧结材料的杨氏模量、切变模量及泊松比与孔隙度的关系.制备了三种钢粉,在不同条件下进行了压制、烧结与热处理.孔隙度对杨氏模量、切变模量及泊松比的影响最大.特别是泊松比还受孔隙形状的影响,而孔隙形状随粉末类型、烧结温度与烧结气氛及热处理条件而变化.对于大部分实际应用的粉末组成来说,烧结气氛对经烧结和热处理后材料的泊松比影响不大.对于部分预合金化粉末(Fe4%Ni1.5%Cu0.5%Mo)+0.8%石墨,只有在孔隙度低于20%时,烧结温度对泊松比与孔隙度的关系才有影响.在这种情况下.提出了烧结与热处理试样泊松比与孔隙度关系的较简单近似方程:在烧结温度1 423K下,v=0.300-0.266P+0.579P2;在烧结温度1 523K下,v=0.304-0.264P+0.548P2.     

Simple low-vacuum coating of paraffin wax on carbonaceous gas sensing layers

A simple low-vacuum coater has been fabricated by using a vacuum resin degassing chamber, in which an aluminum effusion cell is heated by a soldering iron. Our developed vacuum coater presents the versatile methods for depositing paraffin wax for skin-coating the sensing layers of quartz crystal microbalance (QCM). As the increase of the cell temperature, the thickness and inhomogeneity of the wax films were increased. Impedance analyses revealed that the energy dissipation of the QCM was remarkably enhanced with the amount of wax. It was also revealed that the as-deposited wax was fluidic until coagulation by heat radiation. This surface skin coating enhanced the ethyl acetate (EA) sorption capabilities of the polyethylene-sputtered QCM sensor, whereas, it reduced the EA sorption capacity of the d-phenylalanine-sputtered QCM sensor.     

X-ray photoelectron spectrum of Fe2+ state in iron oxides

As a standard for identification of iron oxides by X-ray photoelectron spectroscopy, Fe²⁺ spectra are extracted from mixed Fe 2p_3/2 spectra of Fe³⁺, Fe³⁺ and metallic states. The peaks of Fe²⁺ spectra are all located at binding energy of 708·5 eV. The width of Fe²⁺ spectrum seems to be dependent on crystallinity, and is 2·2 eV for a bulk crystalline oxide and 2·9 eV for an amorphous thin film under instrumental condition with FWHM of 1·3 eV for Au 4f_7/2.     

The mechanism of atmospheric rusting and the protective amorphous rust on low alloy steel

Atmospheric rusting of mild and low alloy steels was studied by means of infra-red and far infra-red spectrophotometries, X-ray and electron diffraction methods and scanning electron microscopy. The rusting process can be interpreted on the basis of a previously reported diagram for rust formation in aqueous solution.A large amount of amorphous matter in rust formed in semi-rural atmosphere was identified by infra-red and far infra-red spectra as amorphous ferric oxyhydroxide, FeO_x (OH)_8–2x. The amorphous ferric oxyhydroxide rust on low alloy steel was dense and uniform, and contained a considerable amount of bound water. From these results it can be concluded that the amorphous ferric oxyhydroxide rust acts as a protective barrier against atmospheric rusting of the steels. Cu, P and Cr in low-alloy steels are inferred to favour the formation of crack-free, uniform rust layer and help to produce uniform amorphous ferric oxyhydroxide.     

Synthesis of polyamide-hydroxyapatite nanocomposites

Simultaneous one-pot syntheses of PA66 and HAp were carried out by extracting H₂O and CO₂ from PA66 monomers and HAp raw materials, respectively, resulting in the formation of a polyamide (PA) 66-hydroxyapatite (HAp) nanocomposite. During the process, a spherical nano-sized HAp particle was precipitated following dissolution of micro-sized CaHPO₄・2H₂O. The PA66 monomers were subsequently adsorbed onto the generated HAp product. Some of the adsorbed PA66 monomers formed a bound polymer on HAp, and an increase in the adhesiveness of the PA66-HAp interface was observed as the polymerization progressed. During this process, the synthesis of a nanocomposite from a micro-sized raw material and creation of an autonomous strong interface between the matrix and filler was achieved. In addition, the shape of the resultant HAp was controllable and could be modified to needle shape by the addition of F⁻ and Mg²⁺ ions to the raw material. HAp could also be changed to plate shape via octa-calcium phosphate (OCP). Notably, during the synthesis, the filler shape of the nanocomposite could be controlled to 0D (particle), 1D (needle), and 2D (plate).     

Solvent Extraction of Indium,Gallium, and Zinc Ions with Acidic Organophosphates having Bulky Alkyl Groups

The extraction equilibria of In³⁺, Ga³, and Zn²⁺ with bis(4‐ethylcyclohexyl)phosphoric acid (D4ECHPA), bis(4‐cyclohexylcyclohexyl)phosphoric acid (D4DCHPA), and bis(2‐ethylhexyl)phosphoric acid (D2EHPA) were investigated in acidic aqueous sulfate media. The order of extractability of metal ions is D4DCHPA > D2EHPA > D4ECHPA, which corresponds to the lipophilicity (log P) of the extractants. The separation factors, β_(In/Ga) and β_(Ga/Zn), of D4ECHPA and D4DCHPA are greater or comparable than that of D2EHPA, because of the steric hindrance of the bulky cyclohexyl groups. In³⁺ can be therefore separated from simulated liquor containing a high concentration of Zn²⁺ by D4DCHPA.     

Characterization of oxygen-dependent lysis of Escherichia coli cells infected by bacteriophage T4

Infection of Escherichia coli cells by T4 phage at a multiplicity of infection (MOI) of 0.01 caused inhibition of cell lysis for up to 4 h. Such cells grown under aerobic condition were lysed by external stimuli such as cold shock, osmotic shock or addition of toxic substances, e.g., carbonyl cyanide m-chlorophenylhydrazone (CCCP). However, the effects of these external stimuli were reduced by transferring the cells to static incubation, by which dissolved oxygen was consumed by the cells within 10 min. The cells became insensitive to such external stimuli when the culture was deoxygenated with nitrogen gas. Following infection with a lysozyme amber mutant, eL1a, the cell membrane permeability was found to be increased either by cold shock or osmotic shock treatment of cells grown under aerobic conditions, but not in cells transferred to the static incubation. Oxygen limitation was suggested to enhance membrane stability in relation to cell lysis following the cold or osmotic shock treatment.     

An XPS study of the surfaces on Fe-Cr,Fe-Co and Fe-Ni alloys after mechanical polishing

Using an XPS technique, the composition and thickness of the surface film and the composition of the underlying alloy surface on Fe-Cr, Fe-Co and Fe-Ni alloys were studied after polishing with silicon carbide paper in trichloro-ethylene and cyclohexane. The compositions of the underlying alloy surface after polishing were almost the same as those of the bulk alloys but the film compositions depended on the alloying addition and environment during polishing. The cationic fractions in the surface films on the Fc-Cr alloys polished in both solvents were almost the same as the corresponding atomic fractions of the bulk alloys. In contrast, iron ions were apt to be concentrated in the surface films on the Fe-Co and Fe-Ni alloys, and the weights of nickel ions were different in the surface films on the Fe-Ni alloys polished in different solvents. Chloride ions were found in the surface films due to the reaction of the metal surface with trichloro-ethylene. The amount of chloride ions was particularly large in the surface films on the Fe-Ni alloys. Heating the alloy specimens under the vacuum of the spectrometer resulted in almost complete reduction of the surface films on the Fe-Co and Fe-Ni alloys, and in the change in the compositions of all alloy surfaces.