Tuning catalytic performances of cobalt catalysts for clean hydrogen generation via variation of the type of carbon support and catalyst post-treatment temperature

Multi-walled carbon nanotubes, three types of activated carbons, single wall carbon nanotube and reduced graphene oxides were used to synthesize nano-sized Co catalysts for H₂ preparation via NH₃ decomposition. Catalyst samples were characterized by number of techniques such as N₂ physisorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopes (XPS), Transmission electron microscopy (TEM), CO chemisorption, temperature-programmed reduction (H₂-TPR) and temperature-programmed desorption (N₂-TPD). The catalytic activities of the studied catalysts for H₂ production via NH₃ decomposition were measured in a fixed-bed micro-reactor. Co catalyst supported on multi-wall carbon nanotubes has shown the highest catalytic activity. The Co particles size was significantly affected by the variation of the post-treatment temperature. The Co particles size in the range of 4.7–64.8 nm can be effectively controlled by varying post-treatment temperature between 230 and 700 °C. The maximum TOF of NH₃ decomposition was registered on cobalt catalyst post-treated at 600 °C.     

Structural change in mercerized cotton fibers on cellulase treatment

Cotton fibers treated with liquid ammonia and sodium hydroxide were hydrolyzed with crude cellulase. The structural change in the fibers due to the cellulase treatment was examined in relation to the apparent affinity of Congo Red. The cellulose III crystalline structure collapsed and generated intermediate‐molecular‐ordered regions on cellulase treatment. Adsorption of Congo Red occurred on the crystallite surfaces of cellulose II and cellulose III that was transformed from cellulose II. The fiber, the dominant crystallite phase of which was cellulose III that was transformed from cellulose II, had a considerably increased apparent affinity after cellulase treatment. The intermediate structure on the crystallite surface was associated with the adsorption of Congo Red in the cases of cellulose II and cellulose III. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 1675–1680, 2001     

Piezoelectric properties of langasite group based on the ionic size of cation

As langasite A₃BC₃D₂O₁₄ compounds group with piezoelectric properties has no phase transition up to the melting point of 1400–1500 °C, they have been applied for the combustion pressure sensor. As they also have a larger electromechanical coupling factor compared to quartz and nearly the same temperature stability as quartz, the surface acoustic wave (SAW) filters are expected based on the digital transformation of wider bandwidth and higher-bit rates. In the case of three-element compounds such as [R₃]_A[Ga]_B[Ga₃]_C[GaSi]_DO₁₄ (R=La, Pr and Nd), the piezoelectric constant increases with the ionic radius R. In the case of four-element compounds such as [A₃]_A[B]_B[Ga₃]_C[Si₂]_DO₁₄ (A=Ca or Sr, B=Ta or Nb), |d₁₁| and k₁₂ values as a function of A_L/B_L ratio showed a linear relationship completely. There are two effects for the substitutions of A- and B-site cations: the substitution of Sr for Ca brings expansion toward [100] and enlargement in |d₁₁| and k₁₂. On the other hand, as the substitution of Ta for Nb brings not much change, the properties are similar. In this study, five-element compounds such as La_3?xSr_xTa_yGa_5?x+ySi_1+x?2yO₁₄ (0≤x≤3, 0≤y≤1) solid solutions analysed by a single crystal X-ray diffraction are compared with the three- and four-element compounds on the coordinates of oxygen ions. As the coordinates positions are located on the extended line of coordinate positions on the three-element compounds as increasing ionic radius of R-ions in A-site, the piezoelectric properties |d₁₁| and k₁₂ are expected become large.     

Calibration of multiple kinects with little overlap regions

When using multiple Kinects, there must be enough distances among neighboring Kinects to avoid spoiled range data caused by the interference of their infrared speckle patterns. In the arrangement, their overlapped regions are too small to apply existing calibration methods using correspondences between their observations straightforwardly. Therefore, we propose a method to calibrate Kinects without large overlapped regions. In our method, first, we add extra RGB cameras in an environment to compensate overlapped regions. Thanks to them, we can estimate their camera parameters by obtaining correspondences between color images. Next, for accurate calibration, which considers range data as well as color images of Kinects, we optimize the estimated parameters by minimizing both the errors of correspondences between color images and those of range data of planar regions, which exist in a general environment such as walls and floors. Although our method consists of conventional techniques, its combination is optimized to achieve the calibration. © 2015 Institute of Electrical Engineers of Japan. Published by John Wiley & Sons, Inc.     

Categorical formulation of mathematical design theories applied to system design process analysis

Given hierarchical system specifications, embodiment and integration processes of subsystems are crucial in designing complex engineered systems. To complement the current mathematical design theories that do not sufficiently support these processes, this study applies general design theory to formulate these processes based on the mathematical structure of design knowledge studied in the literature using category theory. Specifically, the composition of embodiment operations and the relations among subsystems in integration operations on the category of sets and topological spaces are elucidated. Furthermore, the formulation is applied to analysis of a system design process of a production line in model-based systems engineering.     

Synthesis of Ti-based bulk quasicrystal by shock compression

We attempted to produce a Ti₄₅Zr₃₈Ni₁₇ bulk icosahedral (i) quasicrystal by a shock compression technique, in which a single-stage powder gun discharges a flyer plate that consolidates the target powders. The results were also compared with those by a conventional hot-pressing. The powder mixtures for the shock compression were blended by two kinds of methods; that is, gently mixing in a vial, and mechanically alloying by a planetary ball mill. A large bulk i-phase sample, with a Ti₂Ni crystal phase, was synthesized from mechanically alloyed powders after shock compression at a higher flyer velocity, although the conventional hot-pressing at 3 MPa synthesized only the Ti₂Ni phase. For the gently mixed powders, no reaction occured even after shock compression. High-pressure and high-temperature produced during shock compression, and milling process were key factors to obtain the i-phase. The Vickers hardness and the wetting contact angle with pure water under an atmospheric pressure for the bulk sample containing the i-phase were about 7 GPa and about 70°, respectively.     

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.