Fabrication of BSCF-based mixed oxide ionic-electronic conducting multi-layered membrane by sequential electrophoretic deposition process

The Ba_0.5Sr_0.5Co_0.8Fe_0.2O_3-δ (BSCF)-based multi-layered oxygen separation membrane was fabricated by the sequential electrophoretic deposition (EPD) process. A thin porous/dense bi-layer of BSCF was formed on a thick porous support of BSCF. The porous support prepared by a sacrificial template method using BSCF powder mixed with wheat starch (30 wt%) as a pore-forming agent, followed by uniaxial pressing and low-temperature sintering, was directly used as an EPD electrode. A thin BSCF layer was first formed on the porous support, and then a thin BSCF + PMMA (polymethyl methacrylate) layer was sequentially formed on the thin BSCF layer using a bimodal suspension of BSCF and PMMA. A 30-μm thin porous/dense bi-layer of BSCF of which the total thickness was obtained by optimizing the processes of EPD and subsequent co-sintering. The oxygen separation performance of 3.7 ml (STP) min^?1 cm^?2 at 860 °C was achieved for the BSCF-based multi-layered oxygen separation membrane.     

Structure,transport properties,and dielectric properties of lactic acid/pyruvic acid aqueous solution in a biofuel cell: A molecular simulation study

Molecular dynamics (MD) simulation of lactic acid (L‐acid) and pyruvic acid (P‐acid) in a physiological salt solution has been performed, which is used as the electrolyte in a sort of biofuel cell working on a human skin. The structure, frequency distribution of molecules, dielectric properties, rotational correlation functions, and diffusion coefficients have been calculated. The anomalous behavior of dielectric constants for the lower concentration of L‐acid and P‐acid has been obtained from MD. The anomalous dielectric constant is discussed in relation with the various physical properties of the solution including the life time of the interaction in the solution. MD results suggest that the anomalous behavior is supposed to be attributed to the difference of interactions between ions in the lower and higher concentration region. POLYM. ENG. SCI., 59:2474–2478, 2019. © 2019 Society of Plastics Engineers     

Strength of spline joints assembled by forming

In this paper, a new assembling method of spline joints that enables tight fitting in a simple manner by allowing slight plastic deformation at the spline teeth was introduced. Experiments were carried out for the spline joints of medium carbon steel varying the overlap zone between the male and the female spline teeth. Axial joining strength was increased with increase in the overlap length due to the residual compressive stress by forming. The joint by the proposed method also showed higher torsional strength than the conventional joint. Improvement in the torsional strength was explained based on the deformation and hardness distribution around the spline teeth. With respect to the shape of overlap zone, better results were obtained when using the specimen having a uniform overlap length along the axial direction.     

Structure and physical properties of dried Tetra-PEG gel

We investigated crystal structure, and thermal, swelling, and deformation behaviors of dried tetrafunctional (polyethylene glycol) gel, Tetra-PEG gel, with narrow molecular distribution. Tetra-PEG gel consists of two kinds of symmetrical tetrahedron-like PEG macromonomers with a fixed molecular weight. In spite of network structure with rather small molecular weight between cross-links (M_c) (≈5000), the dried Tetra-PEG gels were found to be capable of crystallization. The crystalline melting temperature (T_m) and the degree of crystallinity (X_c) of dried Tetra-PEG gels obtained by differential scanning calorimetry (DSC) were substantially constant against the polymer volume fraction at preparation (?₀). Furthermore, the corrected elastic modulus (G) of dried Tetra-PEG gels did not depend on ?₀. These experimental results indicate that the there exist negligible entanglements in the dried Tetra-PEG network irrespective of ?₀. In other words, Tetra-PEG gels do not have significant topological inhomogeneities.     

Material performance of age-hardened beryllium–copper alloy,CDA-C17200, in a high-pressure,gaseous hydrogen environment

In order to develop safer and more energy-efficient, hydrogen pre-cooling systems for use in hydrogen refueling stations, it is necessary to identify a high-strength metallic material with greater thermal conductivity and lower susceptibility to hydrogen embrittlement, as compared with ordinary, stable austenitic stainless steels. To accomplish this task, the hydrogen compatibility of a precipitation-hardened, high-strength, copper-based alloy was investigated by slow-strain-rate tensile (SSRT), fatigue-life, fatigue-crack-growth (FCG) and fracture toughness tests in 115-MPa hydrogen gas at room temperature. The hydrogen solubility and diffusivity of the alloy were also determined. The hydrogen solubility of the alloy was two or three orders of magnitude lower than that of austenitic stainless steels. The alloy also demonstrated absolutely no hydrogen-induced degradation of its strength properties, a factor which could contribute to the reduction of costs related to the construction and maintenance of hydrogen refueling stations, owing to the downsizing and improved cooling performance of the pre-cooling systems.     

Thermal Decomposition of Titanium Alkoxide and Silicate Ester in Organic Solvent: A New Method for Synthesizing Large-Surface-Area, Silica-Modified Titanium(IV) Oxide of High Thermal Stability

Silica-modified titanium oxide (S-TiO₂) powders that have an anatase structure were synthesized via the thermal decomposition of mixtures of titanium(IV) isopropoxide (TIP) and tetramethyl orthosilicate (TMOS) in toluene at 300°C. These S-TiO₂ materials had high rutile-transformation temperatures and maintained large surface areas at elevated temperatures (550°–1000°C). For example, the product that was prepared from a 9:1 TIP:TMOS mixture transformed to rutile at ∼1100°C and possessed a surface area of 160 m²/g, even after calcination at 800°C for 1 h.     

Molecular Dynamics Study of Atomic Structure and Diffusion Behavior in Amorphous Silicon Nitride Containing Boron

We have performed molecular dynamics simulations of amorphous Si₃N₄ containing boron (Si-B-N). We have examined short-range atomic arrangements and self-diffusion constants of amorphous Si-B-N systems with various boron contents. Our simulations show that boron atoms are threefold coordinated by nitrogen atoms and that nitrogen atoms are bonded to both silicon and boron atoms in the amorphous network of Si-B-N. Also, the self-diffusion constant of nitrogen in Si-B-N is much decreased compared with that in amorphous Si₃N₄. This suggests that boron is important in decreasing the mobility of atoms in amorphous Si-B-N, which may explain the improved thermal stability of amorphous Si-B-N relative to amorphous Si₃N₄ observed experimentally.