Carbon coating of anatase-type TiO2 through their precipitation in PVA aqueous solution

Fine particles of photocatalytic anatase-type TiO₂ prepared through hydrolysis of titanium-tetraisopropoxide were coated by carbon through their precipitation in poly(vinyl alcohol) (PVA) aqueous solution, followed by heat treatment at high temperatures of 400-1000 °C in a flow of high purity Ar. Without carbon coating, the phase transformation from anatase to rutile started above 600 °C, but it was suppressed up to 800 °C with carbon coating. Suppression of the phase transformation depended on the amount of carbon coated, apparent suppression being observed with carbon content above 5 mass%. The amount of carbon coated on anatase was controlled by changing the concentration of PVA in the solution. In order to have a carbon content of about 5 mass%, a PVA solution with more than 2 mass% had to be used.     

Si-C-O glass-like compound/exfoliated graphite composites for negative electrode of lithium ion battery

Two low molecular weight silicone compounds, a cyclic type having vinyl groups and a chain-type having Si-H bonds, a catalyst for curing, and a catalyst regulator were mixed. The mixture was impregnated into exfoliated graphite (EG) by sorption, and cured in air at 200 °C. By this process cross-linked silicone coatings were formed on graphite flakes. The composites of Si-C-O glass-like compounds and EG were synthesized by heat treatment of this precursor at 1000-1400 °C for 1 h in argon. The composites formed at 1000-1300 °C were amorphous by XRD and had practically the same chemical composition: Si 44-45, C 27-29, O 25-26, H < 0.5, all in mass%. The ²⁹Si MAS-NMR spectra indicated that the compound formed at 1000 °C was mainly composed of siloxane bonds and amorphous silica, whereas in the compound formed at 1300°C, Si-C bonds and amorphous silica were predominant. The insertion/extraction characteristics of lithium ions for the electrode prepared with composite:poly(vinylidene fluoride) = 90:10 mass% were examined in 1 mol L⁻¹ LiClO₄ solution of ethylene carbonate:diethyl carbonate = 50:50 vol%. High, 650-700 mA h g⁻¹, capacities and steady cycle performance at 50 mA g⁻¹ were achieved with the composites formed at 1250-1300 °C. Capacities of the composites formed at 1200 °C and lower were initially higher but decreased with increasing number of cycles. The composites formed at 1350 °C showed good cycle performance but the capacity was about 500 mA h g⁻¹ due to the formation of β-SiC. Except for the first cycle, the capacity-potential characteristics were similar to those of hard carbons and the coulomb efficiency was 95-100%. For all the composites the capacity was larger than that of graphite (372 mA h g⁻¹) in the range of 50-200 mA g⁻¹. Due to the large insertion capacity of the first cycle, the efficiency was low (60-70%) at first. By short-circuiting the working electrode to the lithium foil counter electrode for a certain period, the irreversible capacity of the first cycle was almost eliminated. It indicates that direct doping of lithium ions into composites is a promising way to increase the efficiency of the first cycle.     

The kinetics of phenol decomposition under UV irradiation with and without H2O2 on TiO2, Fe–TiO2 and Fe–C–TiO2 photocatalysts

H₂O₂ used in the photo-Fenton reaction with iron catalyst can accelerate the oxidation of Fe²⁺ to Fe³⁺ under UV irradiation and in the dark (in the so called dark Fenton process). It was proved that conversion of phenol under UV irradiation in the presence of H₂O₂ predominantly produces highly hydrophilic products and catechol, which can accelerate the rate of phenol decomposition. However, while H₂O₂ under UV irradiation could decompose phenol to highly hydrophilic products and dihydroxybenzenes in a very short time, complete mineralization proceeded rather slowly. When H₂O₂ is used for phenol decomposition in the presence of TiO₂ and Fe–TiO₂, decrease of OH radicals formed on the surface of TiO₂ and Fe–TiO₂ has been observed and photodecomposition of phenol is slowed down. In case of phenol decomposition under UV irradiation on Fe–C–TiO₂ photocatalyst in the presence of H₂O₂, marked acceleration of the decomposition rate is observed due to the photo-Fenton reactions: Fe²⁺ is likely oxidized to Fe³⁺, which is then efficiently recycled to Fe²⁺ by the intermediate products formed during phenol decomposition, such as hydroquinone (HQ) and catechol.     

Occurrence and sources of perfluorinated surfactants in rivers in Japan

We analyzed perfluorinated surfactants (PFSs) in 20 river samples and 5 wastewater secondary effluent samples in Japan to reveal their occurrence and sources. Nine PFS species were determined: perfluorooctanesulfonate (PFOS), perfluorooctane sulfonamide (FOSA), perfluoroheptanoate (PFHpA), perfluorooctanoate (PFOA), perfluorononanoate (PFNA), perfluorodecanoate (PFDA), perfluoroundecanoate (PFUA), perfluorododecanoate (PFDDA), and perfluorotridecanoate (PFTDA). PFSs were detected in all rivers, revealing nationwide contamination of rivers. In particular, 11 out of 20 river samples exceeded New Jersey guidance for PFOA in drinking water (40 ng/L). PFOS, PFHpA, PFOA, and PFNA were major species in Japan. Concentrations of PFOS, PFHpA, and PFNA in rivers were strongly correlated with population density, suggesting that the chemicals were derived from urban activities. PFOA showed a significant but weak correlation. We used crotamiton, a marker of sewage effluent, for further source analysis. Concentrations of PFOS, PFHpA, and PFNAwere strongly correlated with those of crotamiton, and plots of secondary effluents fell near the regression lines of rivers, indicating that the PFOS, PFHpA, and PFNA in rivers were derived from sewage effluent. On the other hand, PFOA was found at remarkably high levels (54-192 ng/L) in seven river samples containing low levels of crotamiton, suggesting that it was derived from nonsewage point sources, as well as sewage effluent. The total fluxes of sewage-derived PFOS, PFHpA, PFOA, and PFNA from Japan were estimated to be 3.6, 2.6, 5.6, and 2.6 t/year, respectively. This is the first report to identify PFOA in several rivers, derived from nonsewage point sources, by using a marker of sewage effluent.     

Photoluminescence Analysis of Iron Contamination Effect in Multicrystalline Silicon Wafers for Solar Cells

We investigated the effect of Fe contamination on the electronic properties of dislocation clusters in relation to oxygen precipitation in multicrystalline silicon (mc-Si). Photoluminescence (PL) spectroscopy and mapping were performed at room and liquid-He temperatures on mc-Si wafers before and after Fe contamination. PL spectra consisted of the band-edge emission, the 0.78-eV emission associated with oxygen precipitates, and the dislocation-related D-lines. The Fe contamination increased the electrically active dislocation clusters. Part of these clusters acted as preferential oxygen precipitation sites, and their electronic properties were not further influenced by the Fe contamination.     

Performance of a solid oxide fuel cell couple operated via in situ catalytic partial oxidation of n-butane

The operation of a pair of anode-to-anode-facing solid oxide fuel cells (SOFCs) via in situ catalytic partial oxidation (CPO) of n-butane was investigated. In this simple “no-chamber” setup, butane is partially oxidized by heterogeneous reactions inside the porous anodes, providing processed fuel and the heat required for SOFC operation. The cell couple yielded a power density of up to 270 mW cm⁻², and the maximum total power obtained was 1.2 W with cell sizes of 13 mm × 23 mm. The maximum electrical efficiency was 1.3%. High CO concentrations of up to 1000 ppm were detected in the exhaust gas, indicating that the cell couple could not efficiently consume the complete provided fuel. A flame, lit at the exhaust, minimized the carbon monoxide level while having insignificant influence on the cell performance. Thermal insulation of the cell couple improved the output remarkably, showing the strong influence of temperature on cell performance. The two cells had a distance of only 2 mm, suggesting a potential for high volumetric power densities in multi-cell configurations for a self-sustained combined heat and power system.     

Minimal design for human–agent communication

Robots have been envisaged as both workers and partners of humans from the earliest period in their history. Therefore, robots should become artificial entities that can socially interact with human beings in social communities. Recent advances in technology have added various functions to robots. The development of actuators and grippers show us infinite possibilities for factory automation, and robots can now walk and perform very smoothly. All of these functions have been developed as solutions for improving robot movement and performance. However, there are many remaining problems in the communication between robots and humans. Communication robots provide one approach to the realization of embodied interfaces. Furthermore, the unsolved problems of human–robot communication can be clarified by adopting the concept of subtractive methods. In this article, we consider the minimal design of robots from the viewpoint of designing communication. By minimal design, we mean eliminating the nonessential portions and keeping only the most fundamental functions. We expect that the simple and clean nature of minimally designed objects will allow humans to interact with these robots without becoming uninterested too quickly. By exploiting the fact that humans have “a natural dislike for the absence of reasoning,” artificial entities built according to minimal design principles can extract the human drive to relate with others. We propose a method of designing a robot that has “character” and is situated in a social context from the viewpoint of minimal design. This work was presented in part at the 10th International Symposium on Artificial Life and Robotics, Oita, Japan, February 4–6, 2005     

Mechanical properties of molybdenum neutron-irradiated at a high temperature

Molybdenum specimens prepared by two processes, powder-metallurgy (PM) and electron-beam melting (EB), were irradiated to a fast neutron fluence of 2.74 × 10²⁴n/m² (E_n? 1 MeV) at about 600°C (873 K), and their mechanical properties were studied in detail. It was shown that the degree of irradiation embrittlement in EB-Mo was smaller than that in PM-Mo, which might be caused by stronger grain-boundaries and probably smaller irradiation-hardening in the former. From the relation between the recovery of ductility and microstructural changes in post-irradiation annealed PM-Mo at 800 (1073 K), 1000 (1273 K) and 1200°C (1473 K), it was concluded that the recovery resulted from a decrease of irradiation hardening due to a rearrangement and a disappearance of depleted-zones, dislocation-loops and voids in order with increasing annealing temperature. An anomalous mode of fracture was observed in as-irradiated specimens, which consisted of inhomogeneous deformation, then brittle fracture not at the center but at the root of the deformation neck. This mode was observed in a narrow temperature range near the DBTT. A possible mechanism is discussed.