Preparation and Properties of Bi4 − x Nd x Ti3O12 Thin Films by Chemical Solution Deposition

Neodymium-modified Bi₄Ti₃O₁₂, (Bi, Nd)₄Ti₃O₁₂ (BNT) ferroelectric thin films have been prepared on Pt/TiO_x/SiO₂/Si substrates using metal-organic precursor solutions by the chemical solution deposition method. The BNT precursor films crystallized into the Bi layered perovskite Bi₄Ti₃O₁₂ (BIT) as a single-phase above 600C. The synthesized BNT films revealed a random orientation having a strong 117 reflection, whereas non-substituted BIT thin films exhibited a random orientation with strong 00l diffractions. Among Bi_{4 – x}Nd_xTi₃O₁₂ [x = 0.0, 0.5, 0.75, 1.0] thin films, Bi_3.25Nd_0.75Ti₃O₁₂ thin films showed a well-saturated P-E hysteresis loop with the highest P_r (22 C/cm²) and a low E_c (69 kV/cm) at an applied voltage of 5 V. The Nd-substitution with the optimum amount for the Bi site in the BIT structure was effective not only for promoting the 117 preferred orientation but also for improving the microstructure and ferroelectric properties of the resultant films.     

Solvent effect on cationic polymerization of styrene with α- or β-methylstyrenes

To investigate the steric hindrance in the cationic copolymerization of styrene derivatives, styrene was copolymerized with anethole or with α-methylstyrene in polar and non-polar solvents by using BF₃O(C₂H₅)₂ or SnCl₄-trichloroacetic acid as catalyst. As the polarity of the solvent increased, the relative reactivity of α-methylstyrene towards a styryl cation decreased and that of anethole increased. The mode of attack of the propagating carbocation to styrene derivatives in a non-polar solvent is discussed on the basis of these contrasting phenomena.     

Mixed powder coating film using thermoplastic polyester and its alkaline resistance

To improve alkaline resistance, a newly mixed powder coating film using thermoplastic polyethylene terephthalate (PET) was investigated. Two kinds of polyvinyl butyral (PVB) and two kinds of polyamide (PA) were chosen as the secondary polymer. The melting temperatures (T _ms) of these materials were lower than that of primary PET polymer so the mixed powder coating was able to form a dual phase film through a fluidized bed coating process. Microscope and Fourier transform infrared spectroscopy (FTIR) observations revealed that the dual phase structure was indeed successfully formed and there was a secondary layer over the entire surface area of the film. This mixed powder coating film significantly enhanced the alkaline resistance to an environment filled with NaOH solution at 40°C in which a secondary material would be effective in protecting the film. With regard to both alkaline resistance and film formability, PET/PVB was superior to the PET/PA mixture.     

Synthesis and properties of carbons dispersed with α-iron particles from divinylbenzene-vinylferrocene

α-Iron-dispersed carbon was synthesized, through pressure pyrolysis of divinylbenzene-vinylferrocene above 750°C, and by reduction of magnetite-dispersed carbon. Divinylbenzenevinylferrocene copolymer was pyrolysed at 125 MPa above 750°C to yield carbons dispersed with α-iron accompanied by cementite. Magnetite in the carbon matrix was reduced to α-iron after heat treatments at 500°C in a flow of hydrogen. Carbons synthesized by the pressure pyrolysis of divinylbenzene-vinylferrocene at 800°C and 125 MPa contained iron-compound particles up to 200 nm, whereas the median diameter of α-iron particles in the carbon matrix after reduction treatments was 20 nm. α-Iron-dispersed carbon had a Curie temperature of 770°C. The saturation magnetization of iron-dispersed carbon increased with increasing the pyrolysis temperature of divinylbenzene-vinylferrocene copolymer, and reached a constant value of 183 e.m.u.g⁻¹ at 800°C. The saturation magnetization of α-iron-dispersed carbon after the reduction treatment revealed practically the theoretical value of α-iron. Carbons finely dispersed with only α-iron particles were synthesized successfully by reduction of magnetitedispersed carbons.     

Preparation of Lead Lanthanum Zirconate Titanate (PLZT, (Pb,La)(Zr,Ti)O3) Fibers by Sol-Gel Method

Lead lanthanum zirconate titanate (PLZT, (Pb,La)(Zr,-Ti)O₃) ceramic fibers were prepared by the sol-gel method from a solution of lead acetate trihydrate, lanthanum isopropoxide, zirconium n -propoxide, and titanium isopropoxide that contained 2-methoxyethanol as the solvent. The sols obtained from the solution were concentrated at 156°-174°C for 2 h. Concentration at higher temperatures resulted in more-viscous sols of higher specific gravities. The concentration resulted in the formation of spinnable sols, which had viscosities >10⁵ mPas and exhibited Newtonian flow properties. These spinnable sols were formed to be so stable that no change in viscosity and spinnability was observed for more than three months when stored in a sealed container at room temperature. Gel-to-ceramic fiber conversion was investigated by means of X-ray diffractometry, infrared spectroscopy, and thermal analysis. Single-phase perovskite PLZT ceramic fibers 5-200 μm in diameter and >20 cm in length were obtained. Scanning electron microscopy (SEM) observation and Brunauer-Emmett-Teller (BET) measurement showed that heat treatment of the fibers at a lower rate resulted in the formation of fibers of denser microstructure. Although the SEM image of the cross section of the fibers revealed a relatively dense microstructure and a laser beam could be transmitted through a fiber 6 mm in length, BET measurement of the fibers indicated that the fibers had more than a few percent of open porosities, and scattering of light was observed in the laser-beam guiding test.     

Feasibility of using U to reconstruct close-in fallout deposition from the Hiroshima atomic bomb

The first results on the feasibility of using ²³⁶U to reconstruct the level and spatial distribution of close-in fallout deposition from the Hiroshima A-bomb are reported, coupled with the use of global fallout ¹³⁷Cs and ^239 + 240Pu. The results for global fallout ²³⁶U in soil samples (0-30 cm) from Ishikawa prefecture showed that the deposition density of ²³⁶U from the global fallout can be accurately evaluated using AMS. All deposited ²³⁶U, ¹³⁷Cs and ^239 + 240Pu appeared to have been recovered using 30-cm cores. It was also noted from the depth profiles for ²³⁶U/^239 + 240Pu and ²³⁶U/¹³⁷Cs ratios that the downward behavior of ²³⁶U in the soil was apparently similar to that of ^239 + 240Pu, while the ¹³⁷Cs was liable to be retained in upper layers compared with ²³⁶U and ^239 + 240Pu. The accumulated levels were 1.78 × 10¹³ atoms m^− 2 for ²³⁶U, 4340 Bq m^− 2 for ¹³⁷Cs and 141 Bq m^− 2 for ^239 + 240Pu. The ratios of ²³⁶U/¹³⁷Cs and ²³⁶U/^239 + 240Pu were (4.10 ± 0.12) × 10⁹ and (1.26 ± 0.04) × 10¹¹ atoms Bq^− 1, respectively. Results of ²³⁶U, ¹³⁷Cs and ^239 + 240Pu measurements for the seven soil cores (0-30 cm) from Hiroshima were discussed on the basis of ratios of ²³⁶U/¹³⁷Cs and ²³⁶U/^239 + 240Pu by comparing with those from the background area in Ishikawa, indicating that the global fallout dominates the current level of ²³⁶U accumulation in soil in the Black-rain area around Hiroshima after the Hiroshima bomb, and the contribution of the close-in fallout ²³⁶U produced by the Hiroshima A-bomb seems difficult to observe.     

Nanoparticle formation in H2O/N2 and H2O/Ar mixtures under irradiation by 20 MeV protons and positive corona discharge

To investigate the contribution of ions to gas nucleation, we have performed experiments on the formation of water droplets in H₂O/N₂ and H₂O/Ar gas mixtures by irradiation with a 20 MeV proton beam and by positive corona discharge. The size of the formed nanoparticles was measured using a differential mobility analyzer equipped with a Faraday cup electrometer. Using the proton beam, droplets around 10 nm in diameter were observed for both positively and negatively charged particles, but none were found when the corona discharge was used. This implies the importance of the presence of both positive and negative ions for the formation of nanosize droplets, which attract each other by Coulomb interactions, enhancing the collision frequency and leading to the formation of the 10 nm droplets.     

Estimation of daily intake of phenols in hospital meal samples

Daily intakes of 12 phenols which are possible endocrine disruptors were estimated in hospital meals from 2000 to 2001. 4-Nonylphenol (4-NP (mix)) and bisphenol A (BPA) were detected at levels of 5.0 to 19.4 ng/g and 0.2 to 1.1 ng/g, respectively. 4-tert-Butylphenol, 4-n-pentylphenol, 4 -tert-pentylphenol, 4-n-hexylphenol, 4-n-heptylphenol and 4-tert-octylphenol were detected at levels of 0.1 to 2.4 microg/g. The daily intakes of 4-NP (mix) and BPA were 5.8 microg/day and 0.42 microg/day, respectively. The daily intakes of other phenols were less than 1 microg/day.     

Accelerator-driven system for transmutation of high-level waste

The accelerator-driven transmutation system has been studied at the Japan Atomic Energy Research Institute. This system is a hydrid system which consists of a high intensity accelerator, a spallation target and a subcritical core region. In the conceptual design study, two types of system concepts, sodium cooled and lead-bismuth cooled system, are being studied. In this study, we fucus on our lead-bismuth cooled accelerator-driven transmutation system to investigate basic characteristics. The fuel compositions were optimized for efficient transmutation of minor actinide. The transmutation of long-lived fission products was also considered.