Comments on the evolution of strongly degenerate neutrinos in the early universe

We reconsider the evolution of strongly degenerate neutrinos in the early universe. Our chief concern is the validity of the entropy conservation after the neutrino annihilation process has frozen out (so that the establishment of chemical equilibrium is not trivial). We argue that the entropy indeed conserves because elastic scattering keeps the neutrino and antineutrino distribution functions in the equilibrium form and the sum of their chemical potential keeps zero even after the neutrino annihilation freeze-out. We also simulate the evolution of the degenerate neutrino spectrum to support the argument. We conclude that the change in the neutrino degeneracy parameter when the relativistic degrees of freedom in the universe decreases is calculated using the entropy conservation and the lepton number conservation without worrying about at what temperature the neutrino annihilation process freezes out.     

Gamma-ray spectroscopy of the neutron-rich Ni region through heavy-ion deep-inelastic collisions

Nuclei in the neutron-rich Ni region have been studied by γ-ray spectroscopy. Gamma-rays emitted from isomers, with T _1/2 > 1 ns, produced in heavy-ion deep-inelastic collisions were measured with an isomer-scope. The nuclear structure of the doubly magic ⁶⁸Ni and its neighbor ^69,71Cu is discussed on the basis of the shell model. Future experiments for more neutron-rich Ni nuclei are also viewed. Received: 1 May 2001 / Accepted: 4 December 2001     

Evaluation of fine structure of tubular zeolite NaA membrane by FTIR-ATR and FIB-TEM.

A zeolite NaA (LTA) membrane supported by an alumina porous support tube for pervaporation (PV) dehydration of ethanol was characterized by transmission electron microscopy (TEM) using a focused ion beam (FIB) thin-layer specimen preparation technique and by Fourier transform infrared attenuated total reflectance method (FTIR-ATR) using a diamond prism as the waveguide. FIB-TEM clearly presented cross-section images up to about 15 microm depth from the membrane surface. FTIR-ATR monitored the Si-O asymmetric stretching vibration spectrum. The Si-O spectrum was compared with the TEM image and their relationships were discussed. By combining the two methods, we could study the thickness of surface LTA crystals, the grain boundary, the LTA/alumina interface structure and the crystallinity and density of materials inside of the alumina porous support. Consequently, fine structure changes of the LTA membrane corresponding to the hydrothermal synthesis condition could be sensitively detected.     

Different acute effects of oral and intratracheal administration of disodium arsenate and gallium arsenide on heme synthesis in rats

The acute influences of arsenic compounds on the metabolism of porphyrins and heme in various organs of rats after oral or intratracheal administration of disodium arsenate (Na₂HAsO₄) and gallium arsenide (GaAs) were examined and compared. For the oral administration experiments, 21 or 84 mg of Na₂HAsO₄, or 2 or 4 g of GaAs, per cm³ saline per kg body weight of each animal was administered to Jcl: Wistar male rats and the organs were removed after exsanguination from the vein of the right axilla under anesthesia with ether, 16 h after administration. In the case of intratracheal administration, rats given 8.2 or 16.4 mg of Na₂HAsO₄, or 0.2 or 0.4 g GaAs per cm³ saline per kg body weight were examined under the same experimental conditions as for the administration route. Increase in the body weight of rats was suppressed after intratracheal administration of the two arsenic compounds. In these rats the hematocrit value increased significantly. These changes were not shown by the orally administered rats. Elevation in δ-aminolevulinate synthase (ALA-S, EC 2.3.1.37) activity in erythroblasts by Na₂HAsO₄ was much higher after intratracheal administration than after oral administration. Suppression in the activities of δ-aminolevulinate dehydratase (ALA-D, EC 4.2.1.24) and porphobilinogen deaminase (PBG-D, EC 4.3.1.8) in peripheral erythrocytes by Na₂HAsO₄ and GaAs were stronger by intratracheal administration than by the oral route. Influences of GaAs on the activity of PBG-D in rat liver were shown to be more effective by oral administration than by the intratracheal route. Oral administration of Na₂HAsO₄ and GaAs had a stronger suppression effect on the activities of ALA-D and PBG-D in rat kidney. It seems from these results that the different extents of the influence of arsenic compounds might depend on the routes of intake.     

Phenomenon of labyrinth seal with low static pressure difference and large clearance

This paper discusses the straight-through type labyrinth seal. This labyrinth seal is used for axial flow fans, which h ave an outer ring at the blade tip to seal the clearance between the ring tip and the fan shroud, in order to prevent the reverse flow or leakage. These fans are used for the cooling of automobile radiators . In these cases, the labyrinth seal is used in an extremely low static pressure difference and a large clearance . A significant decrease of the leakage rate was reported even when the labyrinth seal rotated in comparatively low speed in this unique condition according to the authors’ former report. However, this phenomen on is differ ent from past research. Further more the cause of th is phenomenon has not been determined. Therefore, the internal flow was depicted with Computational Fluid Dynamics (CFD) in or der to clarify the ca use of this phenomenon. The results of CFD show that the leakage rate decreases significantly because the carry -over flow is intercepted in the expansion groove. This is the newly discovered phenomenon which occurs under the unique condition of an extremely low differential pressure. It has not been pointed out before as the reason why the rotation decreases the leakage rate.     

Heavy element nuclear chemistry at JAERI

The present status of heavy element nuclear chemistry research at JAERI (Japan Atomic Energy Research Institute) is reviewed. Production of the transactinide nuclei ²⁶¹Rf and ²⁶²Db via the reactions of ²⁴⁸Cm(¹⁸O,5n) and ²⁴⁸Cm(¹⁹F, 5n), respectively, at the JAERI tandem accelerator is reported. Study of the aqueous chemistry of Rf is being carried out with a newly developed rapid ion-exchange separation apparatus. Anion-exchange behavior of Rf in acidic solution is briefly discussed. Recent experimental results on decay studies of neutron-deficient actinide nuclei using the gas-jet coupled JAERI-ISOL are given. We also discuss characteristics of nuclear deformation properties at scission in symmetric and asymmetric fission of actinides. Prospects for studies in the near future are briefly considered.     

Cluster and periodic DFT calculations of adsorption and activation of CO2 on the Cu(hkl) surfaces

The adsorption behavior and thermal activation of carbon dioxide on the Cu(1 1 1), Cu(1 0 0), and Cu(1 1 0) surfaces have been investigated by means of density functional theory calculations and cluster models and periodic slabs. According to the cluster models, the optimized results indicate that the basis set of C and O atoms has a distinct effect on the adsorption energy, but an indistinct one on the equilibrium geometry. For the CO₂/Cu(hkl) adsorption systems studied here, the final structure of adsorbed CO₂ is near linear and the preferred modes for the adsorption of CO₂ onto the Cu(1 1 1), Cu(1 0 0), and Cu(1 1 0) surfaces are the side-on adsorption at the cross bridge site with an adsorption energy of 13.06 kJ/mol, the side-on adsorption at the short bridge site (13.54 kJ/mol), and the end-on adsorption on the on-top site with C–O bonds located along the short bridge site (26.01 kJ/mol), respectively. However, the calculated adsorption energies from periodic slabs are lower as compared to the experimental data as well as the cluster model data, indicating that the periodic slab approach of generalized gradient approximation in the density function theory may be not suitable to obtain quantitative information on the interaction of CO₂ with Cu(hkl) surfaces.     

Mass spectrometric studies of alkyl-, phenyl- and chloropyrimidines

The mass spectra of alkyl- and chloropyrimidines are recorded. A generalised fragmentation mechanism for the derivatives of pyrimidine is proposed. The principle of α-cleavage for heterocyclic compounds as proposed in the previous paper is shown to be valid for pyrimidine derivatives. Electronic structures of some molecular and intermediate ions are calculated by the openshell CNDO/2 and INDO methods.