A novel foam based separation strategy for extracting minute target impurities

The purpose of this study was to extract impurities from compounds using a simple separatory bottle to purify target compounds with a foam column and allow for the further characterization of impurities. Charged dyes were used as target compounds due to the ease of detection of dyes and isolated impurities. Foaming agents were used in a glass bottle with a modified cap to separate a target impurity using an appropriately charged ligand. By passing N₂ gas through the solution, the surfactants sodium dodecyl sulfate and cetylpyridinium chloride generated foams that separated the dyes, Methylene blue and Orange G, respectively, from a solution containing both dyes. Sodium dodecyl sulfate condensed Methylene blue from the solution with high purity while cetylpyridinium chloride condensed Orange G with less purity. A range of concentrations (0.01–0.5 mmol/L) of dyes were used for separation. The condensability (volume and/or concentration) of the target compound increased as its concentration decreased. This novel separation method is a simple, rapid, inexpensive, and effective way to prepare samples and allows for the characterization of these impurities using sensitive analytical detection techniques.     

Storage and retrieval of a squeezed vacuum

Storage and retrieval of a squeezed vacuum was successfully demonstrated using electromagnetically induced transparency. The squeezed vacuum pulse having a temporal width of 930 ns was incident on the laser cooled 87Rb atoms with an intense control light in a coherent state. When the squeezed vacuum pulse was slowed and spatially compressed in the cold atoms, the control light was switched off. After 3 mus of storage, the control light was switched on again, and the squeezed vacuum was retrieved, as was confirmed using the time-domain homodyne method.     

Coexistence of covalent superdeformation and molecular resonances in an unbound region of 12Be

The generalized two-center cluster model, which can treat static structures and dynamical reactions in excited states, is applied to the light neutron-rich system, 12Be=alpha+alpha+4N. We discuss the change of the neutrons' configuration around two alpha cores from the covalent structure to the ionic one. We show that, in the unbound region above particle-decay thresholds, the ionic configurations appear as the molecular resonances of alpha+8He, 6He+6He, and 5He+7He. A new type of superdeformation is possible, and we find here a covalent superdeformation with a hybrid configuration of both the covalent and ionic structures. The excitation of these exotic structures through the two-neutron transfer reaction is also discussed.     

Stereodynamics in dissociative adsorption of NO on Si(111)

We report results of our study on the surface-temperature dependence of the steric effect in the dissociative adsorption of NO on Si(111)-(7x7). Data presented here show that, at an incident energy of 58 meV, the reactive sticking probability for the N-end collision is larger than that for the O-end collision. Furthermore, this steric preference is quite sensitive to the surface temperature and the surface coverage. This study shows that the transient surface trapping into a shallow precursor well plays a key role in the stereodynamics of the dissociative adsorption at the low energy region.     

Widely tunable terahertz-wave generation using an N-benzyl-2-methyl-4-nitroaniline crystal

Widely tunable terahertz (THz)-wave generation using difference frequency generation (DFG) in an organic N-benzyl-2-methyl-4-nitroaniline (BNA) crystal was demonstrated. To our knowledge, this is the first report of THz-wave generation by BNA DFG. Large, high-quality single crystals of BNA (phi 8 mm x 30 mm) were grown using the vertical Bridgman method. The nonlinear optical (NLO) coefficient d(33) of the BNA crystal is approximately 234 pm/V, which is the largest value reported for any yellow NLO material. The collinear phase-matching condition of the type-0 configuration is satisfied using a 0.7-1 microm band pump wavelength. We generated THz waves using an organic BNA crystal; the generation range is 0.1-15 THz.     

Direct observation of dispersive Kondo resonance peaks in a heavy-fermion system

Ce 4d-4f resonant angle-resolved photoemission spectroscopy was carried out to study the electronic structure of strongly correlated Ce 4f electrons in a quasi-two-dimensional nonmagnetic heavy-fermion system CeCoGe1.2Si0.8. For the first time, dispersive coherent peaks of an f state crossing the Fermi level, the so-called Kondo resonance, are directly observed together with the hybridized conduction band. Moreover, the experimental band dispersion is quantitatively in good agreement with a simple hybridization-band picture based on the periodic Anderson model. The obtained physical quantities, i.e., coherent temperature, Kondo temperature, and mass enhancement, are comparable to the results of thermodynamic measurements. These results manifest an itinerant nature of Ce 4f electrons in heavy-fermion systems and clarify their microscopic hybridization mechanism.     

Absence of broken time-reversal symmetry in the pseudogap state of the high temperature La(2-x)SrxCuO4 superconductor from muon-spin-relaxation measurements

We have performed zero-field muon-spin-relaxation measurements on single crystals of La(2-x)SrxCuO4 to search for spontaneous currents in the pseudogap state. By comparing measurements on materials across the phase diagram, we put strict upper limits on any possible time-reversal symmetry breaking fields that could be associated with the pseudogap. Comparison between experimental limits and the proposed circulating current states effectively eliminates the possibility that such states exist in this family of materials.     

Water vapor adsorption onto activated carbons prepared from cattle manure compost (CMC)

Activated carbons were prepared from cattle manure compost (CMC) using zinc chloride activation. The structural and surface chemical characteristics of CMC-based activated carbons were determined by N₂ adsorption-desorption and Boehm titration, respectively. The water vapor adsorption properties of the prepared activated carbons with various pore structure and surface nature were examined, and the mechanism of water adsorbed onto activated carbon was also discussed. The results show that the adsorption of water vapor on carbons begins at specific active sites at low relative humidity (RH), followed by micropore filling at medium RH through the formation of pentamer cluster of water molecules in the narrow micropores. The water vapor adsorption capacity of activated carbon is predominantly dependent on its pore volume and surface area. Although capillary condensation is not the mechanism for water adsorption onto activated carbon, water can adsorb on narrow mesopore to some extent.     

Effect of alcohol sources on synthesis of single-walled carbon nanotubes

The effect of oxidant species forming an alcohol molecule for hot-filament chemical vapor deposition (HFCVD) on single-walled carbon nanotubes (SWCNTs) growth has been investigated. To use a graphite rod as a filament for HFCVD to decompose alcohol sources, contamination-free sample surface can be obtained and SWCNTs are successively and densely grown at a lower temperature than those by conventional thermal CVD. It is found that the higher the molecule number of alcohol among CH₃OH, C₂H₅OH, and 2-C₃H₇OH is, the lower the initial growth rate of SWCNTs is. As for CH₃OH, diameter distribution of SWCNTs is dynamically changed with the growth time passed, and a negative growth rate is observed at the later stage of growth. The growth kinetics depending on the alcohol sources is discussed on the basis of a capability of the oxidant species to burn away SWCNTs and deactivation of Co catalysts used for the growth.