Separation of traces of palladium using mercury as collector

Summary Microgram quantities of palladium are quantitatively deposited into mercury globules from various acid solutions. Mercury is removed by evaporation from the resulting amalgam before the subsequent determination.

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Zusammenfassung Mikrogrammengen Palladium werden von Quecksilbertröpfchen aus sauren Lösungen quantitativ extrahiert. Das Quecksilber wird aus dem entstandenen Amalgam vor der Bestimmung des Palladiums abgedampft.

     

<Emphasis Type="Italic">In Situ</Emphasis> Synthesis of Field-responsive Nanocrystalline BaTiO<Subscript>3</Subscript> Particles Modified with Functional Organics

Nanocrystalline BaTiO₃ particles modified with polarizable ligands were synthesized through hydrolysis of modified metal–organics below 100°C. BaTiO₃ precursor was synthesized from barium metal, titanium isopropoxide and polarizable ligands in a mixture of ethanol and 2-ethoxyethanol. The modified Ba–Ti complex alkoxide was hydrolyzed yielding BaTiO₃ particles modified with organics. The crystallinty of nanometer-sized particles was dependent upon the hydrolysis conditions, and increased with increasing water amount and time. The nanocrystalline particles were identified to be BaTiO₃ by X-ray diffraction (XRD) and electron diffraction. A fluid consisting of modified BaTiO₃ particles and silicone oil revealed a typical electrorheological (ER) behavior on applying DC field. The ER behavior was found to depend upon the kind of ligand. 4-Fluorobenzyloxy modifier revealed the highest yield stress in the ER measurement among 4-substitued benzyloxy ligands examined.     

Resolving the discrepancy of 135 MeV pd elastic scattering cross sections and relativistic effects

Three precise measurements for elastic pd scattering at 135 MeV/A have been performed with the three different experimental setups. The cross sections are described well by the theoretical predictions based on modern nucleon-nucleon forces combined with three-nucleon forces. Relativistic Faddeev calculations show that relativistic effects are restricted to backward angles. This result supports the two measurements recently reported by RIKEN and contradicts the KVI data.     

Charge transport in the insulating state of (DMe-DCNQI)2Li above T(SP): a possible fractional charge soliton conduction with +/-1 / 2e

A spin-Peierls system (DMe-DCNQI)2Li is studied with W-band electron paramagnetic resonance (EPR) ( approximately 94 GHz) to unveil a charge transport mechanism in the insulating 4k(F) charge density wave state above T(SP). The electron hopping between the neighbor DCNQI columns provides an additional broadening of the EPR linewidth, since the neighbor columns are generally nonequivalent to each other with respect to g shift. The obtained intercolumn hopping rates lead us to the conclusion that the electron hopping to a hole soliton carrying a fractional charge of e / 2 in the neighbor column dominates the intercolumn charge transport.     

Observation of the "self-healing" of an error field island in the large helical device

It was observed that the vacuum magnetic island produced by an external error magnetic field in the large helical device shrank in the presence of plasma. This was evidenced by the disappearance of flat regions in the electron temperature profile obtained by Thomson scattering. This island behavior depended on the magnetic configuration in which the plasmas were produced.     

Influence of intramolecular vibrations in charge redistribution at the pentacene-graphite interface

We have investigated the relation between the intramolecular vibrational modes of pentacene and the charge redistribution at the pentacene-graphite interface by using high-resolution electron-energy-loss-spectroscopy. The three main vibrational peaks shift to lower energies as the pentacene film thickness decreases. In order to discuss this energy shift, we have calculated the vibrational energies of a free pentacene molecule by changing its charge state. We have also calculated the vibrational energies of a pentacene molecule adsorbed on a graphite sheet by changing the pentacene-graphite distance. Taking the experimental and calculation results into account, we conclude that the observed energy shifts result from an intramolecular charge redistribution. The present results indicate that the effect of an intramolecular charge redistribution is essential to discuss the origin of an energy shift observed in a vibrational study of an organic molecule/substrate interface.     

Multimode optical fiber demultiplexer-star coupler using a single gradient-index-rod lens and a multi-facet grating

An optical fiber multi-function device consisting of a single gradient-index-rod lens and a multi-facet blazed reflection grating is proposed to simultaneously realize functions of wavelength demultiplexing and optical signal distribution in a multimode optical fiber transmission system. We analyzed the demultiplexing characteristics and the tolerance of optical components using the ray trace method. This device can realize not only low loss optical signal distribution but also offers improved demultiplexing characteristics in comparison with the previously proposed demultiplexer-multiposition switch. The following characteristics are expected from the design using commercially available optical components: a working band of 0.64–0.88 μm, channel separation of 34–36 nm, 3 dB bandwidth of 27–28 nm, channel cross-talk of less than - 40 dB and minimum excess insertion loss of 0.9–2.1 dB.     

Controllable photoinduced optical attenuation in a single-mode optical fiber by irradiation of a femtosecond pulse laser

Novel optical attenuation fibers were fabricated by the irradiation of a focused infrared femtosecond pulsed laser onto the core of a silica glass single-mode optical fiber. Optical attenuation at a wavelength of 1.55 microm proportionally increased with increasing numbers of irradiation points and was controllable under laser irradiation conditions. The single-mode property of the waveguide and the mode-field diameter of the optical fiber were maintained after irradiation of the femtosecond laser. It is suggested that the attenuation results from optical scattering at photoinduced spots formed inside the fiber core.     

Towards slow μ− production via muon catalyzed fusion

Slow ^– production via dd-CF using a two-layer arrangement is investigated. To determine its feasibility, experimental measurements are now in progress using the muonic X-ray detection method. The following experimental steps are being considered: (1) measurement of the number of ^– stopped inside a solid H₂/D₂ layer by detecting p K X-rays, (2) hot d emission detection by placing a secondary target at a distance of 10–30 mm from the layer and by detecting specific delayed X-rays, (3) measurement of the disappearance of d emission as the added D₂ layer is increased, (4) dd-CF measurement by detecting fusion protons, and (5) slow ^– emission detection. Results of the initial test experiment are presented.     

Electronic structure of dysprosium silicide films grown on a Si(1 1 1) surface

The thickness-dependent electronic structures of Dy silicide films grown on a Si(1 1 1) surface have been investigated by angle-resolved photoelectron spectroscopy. Two (1×1) periodic bands, both of them cross the Fermi level, have been observed in the silicide films formed by Dy coverages of 1.0 monolayer and below, and more than five () periodic bands have been observed in thicker films. Taking the () periodic structure of Dy atoms in the submonolayer silicide film into account, the periodicity of the two metallic bands indicate that they mainly originate from the orbitals of Si atoms, which form a (1×1) structure. Of the () periodic bands observed in thick films, four of them are well explained by the folding of the (1×1) bands into a () periodicity. Regarding the other band, the three () periodic bands would originate from the electronic states related to the inner Si layers that form a () structure, and the one observed in the 3.0 ML film only might originate from the electron located at the interface between bulk Si and the Dy silicide film.