Collective motion of microspheres in suspensions observed by phase-mode dynamic ultrasound scattering technique

Compared with a nano-sized particle, dynamics of a micron-sized particle in a liquid is often associated with sedimentation (or floating) due to its relatively large mass. The motion of more than two particles is dominated by the hydrodynamic interactions, which are known to persist over a fairly long range, e.g., several millimeters, in suspensions. The particle size may be obtained from the dynamic ultrasound scattering (DSS) technique by the analysis of velocity fluctuations, whose origin is believed to take root in the particle-number fluctuations among temporally formed domains involving collective motion of particles with a certain cut-off length. In this study, such collective particle motion in highly turbid solutions was visualized by means of the phase-mode DSS technique with a single element transducer. Quantitative agreement between the velocity fluctuations obtained by the phase- and conventional amplitude-mode analyses was confirmed, followed by examination of the concentration and the particle size dependences on the dynamic structures induced by the long-ranged interactions. It was found that the phase mode-DSS was a promising method to evaluate the time-dependent structures of the micro-particles in highly turbid suspensions.     

Surface electronic structure of the (3 × 2) reconstruction induced by Yb on a Si(1 1 1) surface

We have investigated the electronic structure of the Yb/Si(1 1 1)-(3 × 2) surface using angle-resolved photoelectron spectroscopy. Five surface states have been identified in the gap of the bulk band projection. Among these five surface state, the dispersions of three of them agree well with those of the surface states of monovalent atom adsorbed Si(1 1 1)-(3 × 1) surfaces. The dispersions of the two other surface states agree well with those observed on the Ca/Si(1 1 1)-(3 × 2) surface, whose basic structure is the same as that of monovalent atom adsorbed Si(1 1 1)-(3 × 1) surfaces. Taking these results into account, we conclude that the five surface states observed in the band gap originate from the orbitals of Si atoms that form a honeycomb-chain-channel structure.     

New labdane diterpenoids from Hyptis fasciculata

Two new labdane diterpenoids, 15beta-methoxyfaciculatin (1) and 15alpha-methoxyfaciculatin B (2), together with the previously known methoxynepetaefolin (3), were isolated from a methanol extract of the dried aerial parts of a Brazilian medicinal plant, Hyptis faciculata. Their structures were elucidated by analysis of spectroscopic data. Plausible biogenetic correlation between faciculatins and nepetaefolin is briefly discussed.     

Practical aspects of ROESY experiments for identification of bound waters in the cyclic tetrasaccharide

ROESY pulse sequences are presented and evaluated to identify bound waters in the cyclic tetrasaccharide. The first experiment incorporated the double-pulsed field gradient spin-echo (DPFGSE) for selective water excitation at the initial portion of the pulse sequence. Although long, shaped pulses were used in DPFGSE to achieve the highly selective excitation of water resonance that is very close to resonances of the cyclic tetrasaccharide, the approach was not effective because of the loss of sensitivity. Concomitant use of long delays and moderate length of shaped pulses in the portion of DPFGSE gained more sensitivity. A simple approach incorporating spin-echo with long delays instead of DPFGSE also afforded a sensitive spectrum. Practical aspects of these ROESY experiments are illustrated using the cyclic tetrasaccharide cyclo-{-->6}-alpha-D-Glcp-(1-->3)-alpha-D-Glcp-(1-->6)-alpha-D-Glcp-(1-->3)-alpha-D-Glcp-(1-->).     

Intercalation of gaseous thiols and sulfides into Ag+ ion-exchanged aluminum dihydrogen triphosphate

Ag(+) ion-exchanged layered aluminum dihydrogen triphosphate (AlP) with the interlayer distance of 0.85 nm was synthesized by the ion-exchange of proton in triphosphate with Ag(+) ion. The amount of exchanged Ag(+) ion depended on the concentration of AgNO(3) aqueous solution. Ag(+) ion-exchanged AlP adsorbed gaseous thiols and sulfides into the interlayer region. The adsorption amounts of thiols were more than those of sulfides, thiols with one mercapto group > thiol with two mercapto groups > sulfides, and depended on the amount of exchanged Ag(+) ion in the interlayer region. The thiols with one mercapto group were intercalated to expand the interlayer distance of Ag(+) ion-exchanged AlP, whereas there was no expansion in the adsorption of sulfide. In the case of thiol with two mercapto groups, there was observed contraction of the interlayer distance through the bridging with Ag(+) ions of the upper and lower sides of the interlayer region.     

New thermal rearrangement of 2H-azirines: Formation of enamines and their cyclization into pyridines

Intermediary formation of enamines in the course of cyclization of vinyl nitrenes into 6-membered ring compounds showed that this reaction proceeded not by insertion but by consecutive hydrogen shift and electrocyclic reaction.     

Diels-alder reactions of 2-pyrones with acyclic dienophiles and hydrolyses of the mono-adducts

Diels-Alder reactions of 2-pyrone (1) with fumaronitrile and maleonitrile afforded regio- and stereo-specific mono-adducts 3a and 3b , respectively. The reaction of 1 with acrylonitrile gave a bis-adduct. The reaction of 4,6-dimethyl-2-pyrone (7) with dimethyl fumarate and dimethyl maleate at higher temperature gave benzene derivatives. The low reactivity of 7 and the instability of the mono-adducts with 7 were considered from the existence of back reaction and easy elimination of methyl formate, respectively. Hydrolyses of the mono-adducts of 2-pyrones gave polyfunctionalized cyclohexenes and elimination products generated from the preferencial trans-elimination of the leaving groups.     

Self-assembled coordination cage derived from small-sized pyridinophane

The dithia[3.3]pyridinophane consisting of two pyridine rings has been found out to assume the syn-structure by the X-ray crystallography, meaning the two nitrogen atoms point in the same direction. From this cyclophane and cis-protected palladium(II), the self-assembled coordination molecular cage has been constructed.     

Study of pyrolysis kinetic of green corn husk

In this paper, it was suggested the use of green corn husk, which is a biomass from agro-industry, as an alternative source of energy through its pyrolysis. Green corn husk characterization was done through immediate and elemental analysis of its components: cellulose, hemicelluloses, and lignin. It was also measured its higher calorific value. The pyrolysis study of green corn husk was done by the isoconversion and the Master plots method. Thermogravimetric plots were obtained at heating rates of 5, 10, 15, and 20 °C min^?1. The pyrolysis kinetics parameters were studied through the Flynn–Wall–Ozawa (FWO), Kissinger, and Friedman models. The Master plots method was used to determine the pyrolysis reaction order. The results of the reaction energy activation were found to be in the range 105.21–157.46 kJ mol^?1 by the FWO method, 150.50 kJ mol^?1 by the Kissinger method, and ranged 120.66–163.81 kJ mol^?1 by the Friedman method. The Master plots method showed a three-way-transport diffusional kinetics for the biomass de-volatilization process. The higher calorific value found for green corn husk was 16.14 MJ kg^?1. The simulation showed correlation between the experimental data and the proposed model for conversion values up to 0.8.