Theoretical validation on the existence of two transverse surface waves in piezoelectric/elastic layered structures

In this paper, we analytically study the dispersion behavior of transverse surface waves in a piezoelectric coupled solid consisting of a transversely isotropic piezoelectric ceramic layer and an isotropic metal or dielectric substrate. This study is a revisit to the stiffened Love wave propagation done previously. Closed-form dispersion equations are obtained in a very simple mathematical form for both electrically open and shorted cases. From the viewpoint of physical situation, two transverse surface waves (i.e., the stiffened Love wave and the FDLW-type wave) are separately found in a PZT-4/steel system and a PZT-4/zinc system. All the observed dispersion curves are theoretically validated through the discussion on the limit values of phase velocity using the obtained dispersion equations. Those validation and discussion give rise to a deeper understanding on the existence of transverse surface waves in such piezoelectric coupled structures. The results can be used as a benchmark for the study of the wave propagation in the piezoelectric coupled structures and are significant in the design of wave propagation in the piezoelectric coupled structures as well.     

Abelianization and Nielsen realization problem of the mapping class group of a handlebody

For the oriented 3-dimensional handlebody constructed from a 3-ball by attaching g 1-handles, it is shown that the natural surjection from the group of orientation preserving diffeomorphisms to the mapping class group has no section when g is at least 5. In order to prove the above result, we show the vanishing of the first homology group with the real coefficient of the mapping class group of the handlebody with genus g at least 3 and a distinguished disk on its boundary.     

Three-dimensional solution structure of bottromycin A2: a potent antibiotic active against methicillin-resistant Staphylococcus aureus and vancomycin-resistant Enterococci

The three-dimensional (3D) structure of bottromycin A(2), a natural anti-methicillin-resistant Staphylococcus aureus (MRSA) and anti-vancomycin-resistant Enterococci (VRE) agent consisting of seven amino acids, has been investigated through NMR spectroscopy. On the basis of 57 experimental constraints, a total of 34 converged structures were obtained. The average pairwise atomic root mean square difference is 0.74±0.59 ? for all heavy atoms. The resulting structure indicates an interesting feature in that the three C-terminal residues of bottromycin A(2) fold back on the 12-membered cyclic skeleton made by the four N-terminal residues. Thus, MePro(2) and Thia-β-Ala-OMe(7), modification of which significantly affects the antibacterial activities of bottromycin A(2), are located on one side of its 3D structure. These distinct structural features might be important for the binding of bottromycin A(2) with the bacterial ribosome.     

Mineral composition of frozen taro for determination of geographic origin

The mineral composition of frozen food of taro [Colocasia esculenta (L.) Schott] was analyzed to categorize the geographical production place of taro. The concentrations of Co and H₂PO₄ ⁻ were found to be useful to separate the producing place between Japan and China. The analysis was performed by instrumental neutron activation analysis (INAA) and ion chromatography (IC). In the case of INAA, the samples were dried and sealed in a vinyl bag and irradiated with thermal neutrons from JRR3M, installed at Japan Atomic Energy Agency (JAEA). The activated samples were cooled down for a few weeks and the elements (Co, Cr, Fe, Rb, Zn) were determined. Cobalt concentration of frozen taro from China was higher than that from Japan. The tendency was the same in the fresh sample of taro. When concentration of H₂PO₄ ⁻ of frozen sample was measured, taro from Japanese product was higher than that of Chinese one, contrary to fresh sample. This result might be caused by the leakage of H₂PO₄ ⁻ during freezing process, indicating that we should be careful to apply the discrimination indicators. In addition to Co, there was a significant difference of Rb and Fe concentrations between frozen taro from Japan and China.     

Synthesis and Aromaticity of Benzene-Fused Doubly N-Confused Porphyrins

A bicyclo[2.2.2]octadiene(BCOD)-fused bis(dipyrromethane) derivative was reacted with methylal in the presence of trifluoroacetic acid followed by oxidation with chloranil to give a doubly N-confused phlorin derivative, which did not undergo the retro-Diels–Alder reaction extruding an ethylene molecule on heating. In contrast, a 7-tert-butoxybicyclo[2.2.1]heptadiene(7-BuOBCHD)-fused bis(dipyrromethane) yielded benzene-ring-fused doubly N-confused porphyrins by following similar reaction sequences.     

Use of 4-bromomethyl-7-methoxycoumarin for derivatization of pyrimidine compounds in serum analysed by high-performance liquid chromatography with fluorimetric detection

Derivatization of the pyrimidine nucleobases and nucleosides with 4-bromomethyl-7-methoxycoumarin was studied with the aim of developing a sensitive and selective column liquid chromatographic method for these substances in serum. The labeling reactions and the nature of derivatives are discussed, together with the chromatographic properties of these derivatives. The derivatives are stable for at least several weeks. Typical detection limits are 50 pg for inosine, 150 pg for uridine, 50 pg for uracil, 50 pg for thymine and 100 pg for fluorodeoxyuridine, respectively. Within-day coefficients of variation averaged 5.0% for the stored-frozen serum pools; the mean day-to-day value was 5.2%. Thirty samples could be processed per working day.     

High-efficiency microcolumn separation of polycyclic arene isomers isolated from carbon black

Summary A packed capillary LC column, featuring 225,000 theoretical plates, was used to resolve numerous polyaromatic isomers (six to nine-ring structures) from an extract of carbon black. Although mass-spectral investigations carried out on the trapped components provide ony tentative identification of large aromatic molecules, improved isomeric resolution through the use of LC microcolumns is a signjifiocant improvement over hitherto used-methods.Dedicated to Profesor A. Zlatkis on the occasion of huis 60th birthday.     

Horse liver alcohol dehydrogenase-catalyzed enantioselective reduction of cyclic ketones: The effect of the hydrophobic side chain of the substrate on the stereoselectivity of the reaction

Horse liver alcohol dehydrogenase (HLADH)-catalyzed enantioselective reductions of alkyl 3-oxocyclopentanecarboxylates, endo-5-acyloxybicyclo[2.2.1]heptan-2-ones and exo-5-acyloxybicyclo[2.2.1]heptan-2-ones gave the corresponding homochiral alcohols and ketones and the interaction between the hydrophobic side chain of the substrate and the hydrophobic zone in the active site played an important role in the specificity of the reduction. The stereoselectivities of the reactions were interpreted on the basis of the cubic space section model and a new rule, which contributes to development of a specificity analysis on the basis of the model, is introduced.     

Gravimetric study of high-pressure sorption of gases in polymers

A gravimetric method for determining precisely the solubility of gases in polymers at high pressure is described. The solubilities of N₂ and CO₂ in low-density polyethylene (LDPE); CO₂ in polycarbonate (PC); and N₂, CH₄, C₂H₆, and CO₂ in polysulfone (PSUL) have been measured as a function of pressure up to 50 atm. Most of the measured sorption isotherms agreed closely with published data, but reproducible and time-dependent hysteresis in the sorption of CO₂, C₂H₆, and CH₄ in glassy polymers, PC, and PSUL, was observed in this study for the first time. Like the well known conditioning effect of high-pressure CO₂ on the sorption capacity of glassy polymers, these hysteresis phenomena are believed to be due to the plasticizing effect of sorbed gases. On the basis of the current data, the dual-mode sorption model including the plasticization by sorbed gas is discussed and a primitive equation for the concentration of sorbed gases in a quasiequilibrium state of sorption or desorption is proposed.