PCE-based fast path control in multi-domain photonic networks

We discuss issues for controlling an optical path in large-scale photonic networks, and introduce an inter-domain path control system based on Path Computation Elements (PCEs). In the system, maximum flow information enables the load balancing of traffic, and Path Key scheme preserve the confidentiality of internal topology information among carrier networks. Based on the experimental results, we show the path setup in the introduced system is significantly faster than the manual path setup among domains in current carriers' networks. For the additional reduction of the path setup time, we propose the domain-wise paralleled signaling method. We also show that decreasing the number of nodes per domain makes path setup faster in the introduced system with deployment of the proposed signaling method.     

Effect of physical mixing of CsCl with Au/Ti-MCM-41 on the gas-phase epoxidation of propene using H2 and O2:: Drastic depression of H2 consumption

Vapor-phase epoxidation of propene using H₂ and O₂ over Au/Ti-MCM-41 with or without a promoter has been investigated at various temperatures and at a space velocity of 4000 h^−1. ml/g (cat). As a promoter, CsCl was impregnated and/or physically (simple mixing) or mechanically (crushed in a mortar) mixed at various concentrations. The support, Ti-MCM-41 (Ti/Si = 3/100), was characterized by XRD, UV-Vis, FT-IR, and specific surface area measurement, whereas Au/Ti-MCM-41 with or without a promoter was characterized by TEM, XPS and ICP techniques before and/or after the catalytic tests. Au/Ti-MCM-41 as such gives propene and H₂ conversions of 3.1 and 47%, respectively, with a PO selectivity of 92% at the reaction temperature of 100°C after 60 min of reaction. Physical mixing of CsCl with Au supported on Ti-MCM-41 reduces H₂ consumption by about 90% and improves propene oxide (PO) selectivity up to 97% at a propene conversion of 1.7%. One constraint is that agglomeration of gold particles is caused by Cl⁻ anions; the mean diameter of Au particles, 2.2 nm, in Au/Ti-MCM-41 increases to about 10–20 nm and some clusters are even larger than 50 nm in size due to direct contact between chloride and Au particles.     

Influence of metal ion concentration in the glycol mediated synthesis of Gd2O3:Eu nanophosphor

The solvothermal synthesis of highly luminescent and homogeneous Gd₂O₃:Eu³⁺ nanophosphor using diethylene glycol as medium, followed by controlled combustion with citric acid as fuel is reported. The influence of concentrations of carboxylic acid and metal cations on the structure, morphology and luminescence properties are investigated in detail. The microscopic investigations indicate the nanocrystalline nature and the strong influence of cation concentration on the size, shape and agglomeration of the particles. It is found that increase in concentration of metal cations lead to the reduction in agglomeration of nanophosphors. The large value of intensity parameter Ω_2, suggested that Eu³⁺ ions reside in a more asymmetric environment, resulted in intense emission due to ⁵D₀–⁷F₂ electric dipole transition. Emission decay analysis of the samples exhibited one exponential nature. The samples prepared under optimum conditions showed a quantum efficiency of 78.63% and a moderately high life time of 1.217 ms.     

Selective catalytic reduction of nitrogen oxides with hydrocarbons over Zn–Al–Ga complex oxides

Selective reduction of NO with hydrocarbons was studied using metal oxide catalysts having a spinel structure. A Zn–Al–Ga complex oxide was found to be very active and selective for the catalytic reduction of NO with both C₃H₆ and CH₄. It was revealed that the role of oxygen at the initial stage of the reaction strongly depends on the reductants; oxygen is mainly used for NO oxidation to NO₂ in the reduction with CH₄, whereas it is used both for NO oxidation to NO₂ and oxidation of C₃H₆ to an active intermediate in the reduction with C₃H₆. This revised version was published online in July 2006 with corrections to the Cover Date.     

Selective catalytic reduction of NO by hydrocarbons on Ga2O3/Al2O3 catalysts

Catalytic properties of supported gallium oxides have been examined for the selective reduction of NO by CH₄ in excess oxygen. The activity was greatly affected by the support; Ga₂O₃/Al₂O₃ (Al₂O₃ supported Ga₂O₃) and Ga₂O₃–Al₂O₃ mixed oxide exhibited high activity and selectivity as comparable to Ga-ZSM-5, while unsupported Ga₂O₃ and the other supported Ga₂O₃ were ineffective. For Ga₂O₃/Al₂O₃, the activity changed with Ga₂O₃ content, and was highest at about 30 wt% Ga₂O₃, which corresponds to a theoretical monolayer coverage. Gallium oxide highly dispersed on Al₂O₃ is considered to be responsible for the high activity and selectivity. The reaction characteristics of Ga₂O₃/Al₂O₃ were studied and compared with Ga-ZSM-5 and Co-ZSM-5. Ga₂O₃/Al₂O₃ exhibited the highest activity and selectivity at high temperature. In addition, Ga₂O₃/Al₂O₃ showed higher tolerance against water than Ga-ZSM-5. C₃H₈ and C₃H₆ were also evaluated as reducing agents, and Ga₂O₃/Al₂O₃ showed higher activity than Ga-ZSM-5 above 723 K achieving almost complete reduction of NO to N₂.     

Improvement in thermal endurance of D-mannitol as phase-change material by impregnation into nanosized pores

This paper describes the control of the melting point and improvement of the thermal endurance of D-mannitol (melting point T_m = 440 K) as a phase-change material (PCM) by vacuum impregnation of the PCM into nanosized pores of porous SiO₂ grains. First, we examined the effects of the average pore size (D_P) of porous SiO₂ on T_m and latent heat (L) of PCM/SiO₂ composites. Second, we investigated the thermal endurance of the composites using constant temperature kinetics based on L of the PCM and composites. Third, we performed cyclic tests of melting and freezing on the composite to evaluate leakage of the PCM. Thermophysical properties of the samples were measured by differential scanning calorimetry, and the following results were obtained: (1) The impregnation ratio of the composites was 0.91–0.99; therefore, almost all pores were completely filled with the PCM. (2) T_m shifted to lower temperature with smaller D_P, reaching 413 K in case of the PCM/SiO₂ composite with a D_P of 11.6 nm (3) T_m was derived as a function of D_P from the Gibbs–Thomson equation taking into account the existence of a nonfreezing layer on the surface of the pore wall. (4) The duration of thermal degradation of the PCM/SiO₂ composite with D_P = 11.6 nm was three times longer than that of the pure PCM at a temperature that is 10 K more than each melting point. (5) The PCM/SiO₂ composite with D_P = 11.6 nm can use as a shape-stable PCM composite without leakage of PCM.     

Vortex Generation in Cyclically Coupled Superfluids and the Kibble-Zurek Mechanism

We study theoretically the generation of cyclic supercurrent among three superfluids coupled by the Josephson Junctions. Depending on the initial relative phases between superfluids, Josephson current flows cyclically through the superfluids to create a quantized vortex. Reducing the coupling strength changes the motion from periodic to chaotic, thus suppressing the cyclic current. Applying this result to the Kibble-Zurek mechanism, the probability of the vortex generation via this mechanism is modified from the simple estimate given by the geodesic rule. We compare our results with the Lancaster, Grenoble and Helsinki experiments.     

Macroscopic Quantum Tunneling of Two-Component Bose-Einstein Condensates

We show theoretically the existence of the metastable state and study the decay through the macroscopic quantum tunneling in two-component Bose-Einstein condensates. The numerical analysis of the coupled Gross-Pitaevskii equations clarifies the metastable states whose configuration preserves or breaks the symmetry of the trapping potential, depending on the interspecies interaction and the particle number. We calculate the tunneling decay rate of the metastable state by using the collective coordinate approximation and the bounce technique. It is found that the macroscopic quantum tunneling is observable in a wide range of the particle number.     

Te concentration dependent photoemission and inverse-photoemission study of FeSe1?xTex

We have characterized the electronic structure of FeSe_1−xTe_x for various x values using soft x-ray photoemission spectroscopy (SXPES), high-resolution photoemission spectroscopy (HRPES) and inverse photoemission spectroscopy (IPES). The SXPES valence band spectral shape shows that the 2 eV feature in FeSe, which was ascribed to the lower Hubbard band in previous theoretical studies, becomes less prominent with increasing x. HRPES exhibits systematic x dependence of the structure near the Fermi level (E_F): its splitting near E_F and filling of the pseudogap in FeSe. IPES shows two features, near E_F and approximately 6 eV above E_F; the former may be related to the Fe 3d states hybridized with chalcogenide p states, while the latter may consist of plane-wave-like and Se d components. In the incident electron energy dependence of IPES, the density of states near E_F for FeSe and FeTe has the Fano lineshape characteristic of resonant behavior. These compounds exhibit different resonance profiles, which may reflect the differences in their electronic structures. By combining the PES and IPES data the on-site Coulomb energy was estimated at 3.5 eV for FeSe.     

Fabrication of silica/platinum core-shell particles by electroless metal plating

An electroless metal plating method was used to form Pt shells on sub-micrometer-sized silica (SiO₂) particles fabricated by a sol-gel method. The electroless metal plating method was comprised of three steps: (1) surface-modification of SiO₂ particles with polyvinylpyrrolidone (PVP) (SiO₂/PVP) or poly-diallyldimethylammonium chloride (PDADMAC) (SiO₂/PDADMAC), (2) pre-deposition of Pt nuclei or Pt fine particles on the SiO₂ particles by reducing Pt ions in the presence of SiO₂/PVP particles (SiO₂/PVP-Pt) or SiO₂/PDADMAC particles (SiO₂/PDADMAC-Pt), and (3) growth of the pre-deposited Pt by immersing the SiO₂/PVP-Pt or SiO₂/PDADMAC-Pt particles in a Pt-plating solution. The pre-deposition of Pt nanoparticles was successfully performed for the surface-modified SiO₂ particles since the surface modification possibly strengthened the affinity between the SiO₂ particle surfaces and Pt ions. The Pt nanoparticles were pre-deposited more uniformly in the case of PVP because the pre-deposition took place more slowly for the PVP, which provided uniform surface-modification followed by the uniform pre-deposition of Pt nanoparticles. The formation of Pt shells was successfully performed on the SiO₂/PVP-Pt particles in the electroless metal plating process because Pt nuclei were generated by the reduction of H₂PtCl₆ and then further deposited on the Pt particle surfaces on the SiO₂/PVP-Pt particles.