Possible 3He Boltzmann Gas Formed on Three-Dimensional Nanopores Preplated with 4He

We have measured the heat capacity of ³He adsorbed on three-dimensionally connected nanopores, 2.7 nm in diameter, preplated with about 1.3 atomic layers of ⁴He. At low coverages of ³He, the ³He heat capacity is roughly constant at the measured temperatures between 0.1 and 1 K. Its molar heat capacity is on the order of the gas constant R, between 1.1R and 1.8R. This suggests a Boltzmann gas state of the adsorbed ³He. At high coverages, the heat capacity is likely approaching linear in T at low temperatures, which suggests a degenerate state at further lower temperatures.     

Depth from Refraction Using a Transparent Medium with Unknown Pose and Refractive Index

In this paper, we introduce a novel method for depth acquisition based on refraction of light. A scene is captured directly by a camera and by placing a transparent medium between the scene and the camera. A depth map of the scene is then recovered from the displacements of scene points in the images. Unlike other existing depth from refraction methods, our method does not require prior knowledge of the pose and refractive index of the transparent medium, but instead can recover them directly from the input images. By analyzing the displacements of corresponding scene points in the images, we derive closed form solutions for recovering the pose of the transparent medium and develop an iterative method for estimating the refractive index of the medium. Experimental results on both synthetic and real-world data are presented, which demonstrate the effectiveness of the proposed method.     

Capillary rise properties of porous mullite ceramics prepared by an extrusion method with various diameters of fiber pore formers

Porous mullite ceramics with unidirectionally oriented pores were prepared by an extrusion method using rayon fibers as the pore formers. Rayon fibers of 8.1, 9.6, 16.8, and 37.6 μm in diameter were used as the pore formers and were kneaded with alumina powder, kaolin clay, China earthen clay, and water to form pastes. These pastes were extruded into cylindrical tubes, dried, and fired at 1500 °C for 4 h. The apparent porosities ranged from 45.7 to 48.2 %. The pore size distributions showed a sharp peak at 9.4, 10.0, 15.6, and 30 μm with increasing fiber diameters. The height of the capillary rise was 1780, 1670, 1320, and 950 mm with increasing fiber diameter. The maximum capillary rise is much higher than previously reported. The contact angle and effective pore radius that determine the capillary rise ability were calculated by fitting the capillary rise curves using the Fries and Dreyer’s equation.     

Preparation method for supported metal catalysts using w/o microemulsion: Study on immobilization conditions of metal particles by hydrolysis of alkoxide

It was previously found that the silica-supported rhodium catalyst prepared using water-in-oil microemulsion had rhodium particles partly, or wholly, embedded in silica. In this work, consequently, we investigated the effect of hydrolysis conditions of tetraethylorthosilicate, employed as the source of silica, on the atomic ratio of surface rhodium in contact with the gas phase, to total surface rhodium of nanoparticles. This ratio is denoted as R in this paper. R became higher when the catalyst was prepared under the following hydrolysis conditions: a shorter hydrolysis time and a smaller amount of tetraethylorthosilicate. On the other hand, R showed the minimum value when the water content in the preparation solution was 33 vol%. From these results, it is demonstrated that it was important to form silica as early as possible in hydrolysis of TEOS in order to increase R values. In addition, the effect of R on the catalytic behavior in CO hydrogenation was investigated. At R values below 30%, the turnover frequencies increased with a decrease in R.     

Preparation of helical carbon and graphite films using morphology-retaining carbonization

Helical carbon and graphite films were prepared from iodine-doped helical polyacetylene (H-PA) film using currently developing morphology-retaining carbonization. It was found from scanning electron microscopy (SEM) observations that the hierarchical helical morphology of the H-PA film remains unchanged even after the carbonization at 800 °C. Besides, the weight loss of the film due to the carbonization was very small, which was only a few percent to the weight of the film before doping. Furthermore, the graphite film prepared by the subsequent heating at 2600 °C still retained the same morphology as those in the original H-PA film and in the helical carbon film prepared at 800 °C. X-ray diffraction (XRD) and Raman scattering measurements were then pursued. The results showed that graphitic crystallization proceeds in the carbon film through the heat treatment at 2600 °C. Transmission electron microscopy (TEM) image of a single helical graphitic fibril was also observed by ultrasonicating the graphite film in ethanol. Carbonization of the H-PA films by way of iodine doping was found to afford helical carbon and graphite films, where spiral morphologies and even helical fibril structures were completely preserved.     

Phase diagram of the Sb2Se3-CuInSe2 pseudobinary system and flux growth of CuInSe2 single crystals

The phase diagram of the Sb₂Se₃-CuInSe₂ pseudobinary system is constructed by using differential thermal analysis and X-ray diffraction. Based on the constructed phase diagram, solution growth of CuInSe₂ crystals is investigated. The grown crystals are evaluated by X-ray diffraction, electron probe microanalysis, Hall effect and inductively coupled plasma measurements. The results indicate that the crystals are not contaminated by the constituent of the flux, i.e., Sb. Hence, Sb₂Se₃ is promising as a solvent for the growth of CuInSe₂ crystals at temperatures lower than 800°C.     

Development of multianode photomultiplier tube

We have developed a multianode photomultiplier tube (MAPMT) which has a sensitive cathode diameter of 36 mm and an anode with 88 segments. The position sensitivity of the tube was studied by using light from a LED and scintillation light from a scintillation-fiber bundle. We observed particle tracks for the first time by using a single photomultiplier tube.     

One-Dimensional Phonon State of 4He Films Adsorbed in Straight Nanopores

We have studied heat capacities of ⁴He adsorbed in straight nanopores 1.8, 2.2, and 2.8 nm in diameter. Heat capacities of the ⁴He fluid film on the solid layer at 0.08–0.4 K show power laws close to T in 1.8 nm pores, close to T ² in 2.8 nm pores, and a crossover from T to T ² with increasing temperature in 2.2 nm pores. These heat capacities are explained by a model assuming a phonon dispersion with continuous one-dimensional (1D) states in the axial direction and discrete energy levels in the azimuthal direction. By fitting experimental data to the model, the phonon velocity along the pore axis and the energy gap for propagation in the cross section are derived. At temperatures sufficiently lower than the energy gap, where the thermal wave length of phonons is much longer than the effective pore diameter, the ⁴He fluid films show a T-linear heat capacity of 1D phonons propagating only along the pore axis. At higher temperatures, a 1D-2D crossover of phonons occurs.      

Limitations of the method using peroxidase activity of hemoglobin for detecting lipid hydroperoxides

The method using peroxidase activity of hemoglobin (Hb) for the determination of lipid peroxides was examined by using pure methyl linoleate hydroperoxides, trilinoleoylglycerol hydroperoxides and egg yolk phosphatidylcholine hydroperoxides as substrates and tetramethyl benzidine as electron donor for the peroxidase reaction of Hb. The reactivities of these substrates were quite varied. Furthermore, some electron donors were tested for peroxidase activity of Hb, but none showed a complete reduction of methyl linoleate hydroperoxides. From these results, it seems the Hb method needs to be carefully applied to biological materials that contain mixtures of different types of lipid classes.     

On-Site Fabrication of Crystalline Cerium Oxide Films and Patterns by Ink-Jet Deposition Method at Moderate Temperatures

Crystalline CeO₂ films and patterns have been successfully fabricated in a "single-step process" at moderate temperature. In this process, the combination of the ink-jet technique and depositing the precursor on a hot substrate (≤300°C) gave crystalline CeO₂ without further heat treatment. X-ray diffraction analysis revealed that the phase formed was crystallized ceria with nanosized (<10 nm) crystallites. The film thickness was several hundred nanometers and the pattern width was about 150 μm. Scanning electron microscopy analysis showed that the films and patterns were free of cracks and adhered to the substrate. This is the first report about the direct patterning of crystalline CeO₂ without postfiring or posttreatments like masking, etching, etc.