Quasisteady high-confinement reversed shear plasma with large bootstrap current fraction under full noninductive current drive condition in JT-60U

A quasisteady reversed shear plasma with a large bootstrap current fraction ( approximately 80%) has been obtained for the first time in the JT-60U tokamak. The shrinkage of reversed shear region was suppressed by the bootstrap current peaked at the internal transport barrier (ITB) layer and the ITBs at a large radius were sustained, which, by combination with an H-mode edge pedestal, resulted in a high confinement or 2.2 times the H-mode scaling for 6 times energy confinement time or 2.7 s. Furthermore, a full noninductive current drive was obtained by the bootstrap current and the beam driven current.     

S<Subscript>3</Subscript> symmetry and neutrino masses and mixings

Based on the universal seesaw mass matrix model with the three scalars φ_i, and by assuming S₃ flavor symmetry for the Yukawa interactions, the lepton masses and mixings are investigated systematically. In order to understand the observed neutrino mixing, the charged leptons (e,μ,τ) are regarded as the three objects (e₁,e₂,e₃) of S₃, while the neutrino mass eigenstates are regarded as the irreducible representation (ν_η,ν_σ,ν_π) of S₃, where (ν_π,ν_η) and ν_σ are a doublet and a singlet, respectively, which are composed of the three objects (ν₁,ν₂,ν₃) of S₃.     

Piezo-optical study of excitons in KI

The effects of a uniaxial stress along 〈001〉 or 〈110〉 direction on the excitonic structures of KI are studied between 5.5 and 7.5 eV at room temperature by a piezo-modulation technique. Stress dichroism leads to the conclusion that either the second or the third peak corresponds to a transition at the Γ point in the Brillouin zone forming a spin-orbit pair with the first exciton and the other to a transition at the L point. The fourth peak is ascribed to a transition at the L point with an overlaping one at the X point.     

A reliable single parameter interatomic potential for argon

A simple semiempirical approximation previously proposed for the isotropic intermolecular forces between two closed shell systems is tested in detail for the argon-argon interaction. The potential is based on the knowledge of the first-order coulomb interaction energy, a suitably damped three term long range asymptotic expansion of the second order coulomb energy, and a semiempirical representation of the exchange interaction energy which contains one adjustable parameter. The single adjustable parameter can be reliably determined by fitting the second virial coefficient for argon in the 130–773 K temperature range with the long range interaction coefficients being constrained within the theoretical bounds specified by Tang, Norbeck and Certain. The reliability of the potential is compared with that of several literature potentials by comparing the theoretical predictions obtained from the potentials with experimental results for the second virial coefficient, viscosity, thermal conductivity and thermal diffusion ratios for dilute argon gas, and with spectroscopic data for the dimer, and with SCF calculations of the Ar-Ar potential at small interatomic separations. Our best potential predicts these properties with a precision as good as or better than other recent potentials which generally contain more adjustable parameters and/or involve more input data. The results confirm earlier work that suggested that the scheme tested is capable of yielding reliable isotropic potentials for the interaction of closed shell systems for 0·3 ? R/R_m ? ∞ where R_m is the intermolecular distance at the van der Waals minimum. The scheme appears to offer a method for obtaining reliable potentials while avoiding problems associated with optimizing many parameters with respect to fitting experimental constraints.     

Komplexe aus Poly-L-glutaminsäure und Oligoäthyleneniminen und deren quaternären Derivate: Einfluß der Kettenlänge der Oligomeren auf die Komplexbildung

Ohne Zusammenfassung     

Intermolecular forces for hydrogen,nitrogen and acetylene

Orientation-dependent intermolecular potentials for H₂, N₂, and C₂H₂ have been determined on the basis of electron charge density contours, octopolar induction in the dispersion force, electrostatic quadrupolar interaction, and the observed second virial coefficients. The recently settled structure of low-temperature solid acetylene has been discussed.     

Neocarzinostatin: selective tryptophan oxidation and neocarzinostatin-chromophore binding to apo-neocarzinostatin

Neocarzinostatin (NCS), an antitumor protein antibiotic, is composed of apo-neocarzinostatin (apo-NCS) and neocarzinostatin-chromophore (NCS-chr), the principle of the biological activities of NCS. Apo-NCS having two tryptophan (Trp) residues at positions (39 and 83) was chemically modified by N-bromosuccinimide in a study on the correlation of the binding site(s) of NCS-chr. Selective oxidation of Trp residues was observed when NCS was titrated with N-bromosuccinimide. In contrast, non-selective oxidation of the two Trps on apo-NCS was observed and both Trp (39 and 83) of apo-NCS were titrated with N-bromosuccinimide. After selective oxidation, the remaining Trp residue of NCS was assigned as Trp (83). These results clearly indicate that the Trp (83) residue of apo-NCS changed from the "reactive type" to the "non-reactive type" after the binding of NCS-chr with apo-NCS. The fluorescence emission intensity of apo-NCS generated from the Trp (39) residue was quenched by NCS-chr. These data suggest that NCS-chr directly interacts with the Trp (39) residue and that a beta-sheeted loop containing the Trp (83) residue of apo-NCS changes the high-order structure upon binding with NCS-chr.