Tunneling chemical reactions in solid parahydrogen: direct measurement of the rate constants of R + H2 --> RH + H (R = CD3,CD2H,CDH2,CH3) at 5 K

Tunneling chemical reactions between deuterated methyl radicals and the hydrogen molecule in a parahydrogen crystal have been studied by Fourier transform infrared spectroscopy. The tunneling rates of the reactions R + H2 --> RH + H (R = CD3,CD2H,CDH2) in the vibrational ground state were determined directly from the temporal change in the intensity of the rovibrational absorption bands of the reactants and products in each reaction in solid parahydrogen observed at 5 K. The tunneling rate of each reaction was found to differ definitely depending upon the degree of deuteration in the methyl radicals. The tunneling rates were determined to be 3.3 x 10(-6) s(-1), 2.0 x 10(-6) s(-1), and 1.0 x 10(-6) s(-1) for the systems of CD3, CD2H, and CDH2, respectively. Conversely, the tunneling reaction between a CH3 radical and the hydrogen molecule did not proceed within a week's time. The upper limit of the tunneling rate of the reaction of the CH3 radical was estimated to be 8 x 10(-8) s(-1).     

Nonlinear resonances and self-excited oscillations of a rotor caused by radial clearance and collision

This paper investigates oscillations in a flexible rotor system with radial clearance between an outer ring of the bearing and a casing by experiments and numerical simulations. The mathematical model considers the collisions of the bearing with the casing. The following phenomena are found: (1) Nonlinear resonances of subharmonic, super-subharmonic and combination oscillation occur. (2) Self-excited oscillation of a forward whirling mode occurs in a wide range above the major critical speed. (3) Entrainment phenomena from self-excited oscillation to nonlinear forced oscillation occur at these nonlinear resonance ranges. Moreover, this study analyzes periodic solutions of the mathematical model by the Harmonic Balance Method (HBM). As the results, the nonlinear resonances of subharmonic oscillation and its entrainment phenomenon can be explained theoretically by investigating the stability of the periodic solutions. The influence of the static force and the bearing damping on these oscillation are also clarified.     

Interspecies comparison of chemical composition and anxiolytic-like effects of lavender oils upon inhalation

Essential oils have traditionally been used for decades to alleviate the symptoms of various mental problems. In terms of anxiolytic-like properties, lavender oil is probably the most commonly used and best-studied essential oil. Although there is compositional variance among the oils extracted from different origins, there have been few studies performed to date to investigate how these differences affect the expression of anxiolytic-like activity. This paper discusses the interspecies differences and contributions of the main constituents in the expression of anxiolytic-like effects upon inhalation, as assessed in mice by the elevated-plus maze test, by comparing the essential oils from six different species of Lavandula. The results showed qualitative and quantitative variations in the tested oils, which results in significant differences in their anxiolytic-like activities. Our findings also suggest that linalyl acetate (LA) works synergistically with linalool (LO) and that the presence of both LA and LO is essential for the whole oil to work as an inhaled anti-anxiety agent.     

Strahlenchemische Untersuchungen von Proteinreaktionen: Einflu? der Atmosph?re und der Temperatur bei der Bestrahlung auf die Spaltung von sekund?ren Bindungen im Protein

Ohne Zusammenfassung     

Strahlenchemische Untersuchungen von Proteinreaktionen: Einflu? von Erdalkalimetallen auf die Brechung von sekund?ren Bindungen im Protein

Ohne Zusammenfassung     

Strahlungschemische Untersuchungen von Proteinreaktionen: Einflu? von Aminos?uren und Vitaminen auf das Aufbrechen von sekund?ren Bindungen im Protein

Ohne Zusammenfassung     

A new structure of water layer on Cu(111) electrode surface during hydrogen evolution

A layered structure of water molecules formed on a Cu(111) electrode surface during hydrogen evolution in sulfuric acid solution was studied by surface X-ray diffraction and infrared reflection absorption methods. Water molecules in the surface layers take a closest pack-like stacking structure with nearest-neighbor oxygen-oxygen distances in intra-(0.322(5) nm) and inter-(0.275(15) nm) layers of multi-domains; the infrared spectra of the layered water on the Cu electrode surface showed the existence of free OH(OD) and hydrogen-bonded OH(OD) of water molecule.     

Nuclear spin conversion of methane in solid parahydrogen

The nuclear spin conversion of CH(4) and CD(4) isolated in solid parahydrogen was investigated by high resolution Fourier transform infrared spectroscopy. From the analysis of the temporal changes of rovibrational absorption spectra, the nuclear spin conversion rates associated with the rotational relaxation from the J=1 state to the J=0 state for both species were determined at temperatures between 1 and 6 K. The conversion rate of CD(4) was found to be 2-100 times faster than that of CH(4) in this temperature range. The faster conversion in CD(4) is attributed to the quadrupole interaction of D atoms in CD(4), while the conversion in CH(4) takes place mainly through the nuclear spin-nuclear spin interaction. The conversion rates depend on crystal temperature strongly above 3.5 K for CH(4) and above 2 K for CD(4), while the rates were almost constant below these temperatures. The temperature dependence indicates that the one-phonon process is dominant at low temperatures, while two-phonon processes become important at higher temperatures as a cause of the nuclear spin conversion.