Determination of dissolved natural thorium and uranium in Horonobe and Mizunami Underground Research Laboratory groundwater and its thermodynamic analysis

At two underground research laboratories situated at Horonobe and Mizunami, Japan, trace amounts of natural thorium and uranium dissolved in deep groundwater were investigated with the help of chemical pre-concentration method. The groundwater was sampled from underground boreholes under the geochemical condition of no atmospheric exposure, and the colloid contribution was checked by in situ two size-fractionated ultrafiltration systems. A rough decrease by half in the concentration after in situ filtration suggested the presence of natural colloids and suspended matter that were carriers of a portion of the elements. The Th and U concentrations in groundwater after 10 kDa filtration was evaluated as dissolved species, and was identified thermodynamically using existing hydrogeological and geochemical data, such as the mineral components in the groundwater at a given pH, ionic strength, concentration of co-existing ions, redox potential, and a hypothetical solubility-limiting solid phase. The crystalline solid phase of tetravalent thorium and uranium dioxides made the solubility very low compared with that of the amorphous phase.     

Effect of anisotropic scattering in neutronics analysis of BWR assembly

The anisotropic scattering effect to keff is studied for UO₂ and MOX fueled BWR assemblies. The anisotropic scattering effect increases the assembly k_∞ by 0.44% Δk for the UO₂ assembly with 0% void fraction, and by 0.21% Δk for the MOX assembly with 0% void fraction. This is because the anisotropic scattering effect flattens the intra-assembly thermal flux, and the absorption rate in the surrounding water gap is decreased, but the absorption rates in the MOX fuel rods are increased compared to the UO₂ rods. Therefore, the total decrease in absorption rates in the UO₂ assembly is relatively large, and the k_∞ is increased in the UO₂ assembly. The dependence of the anisotropic scattering effect on the void fraction is investigated, and the significant difference of 0.62% Δk/k is found for the 0% and the 80% void fractions. The BWR assemblies with Gd rods are also considered. Furthermore, the usefulness of the transport cross section is investigated, and it is found that the transport cross section gives reasonable anisotropic scattering effect, though not satisfactory.     

Intake of different eicosapentaenoic acid-containing lipids and fatty acid pattern of plasma lipids in the rats

The ethyl ester of eicosapentaenoic acid (EPA) is the only pure EPA-containing lipid available in bulk for oral administration. However, there is doubt as to whether EPA ethyl ester can efficiently increase the plasma levels of EPA in comparison with the ability of other kinds of EPA-containing lipids to do so. Therefore, two other kinds of EPA-containing lipids were prepared to study the efficiency of oral administration of those lipids for increasing the EPA content in plasma phospholipids and cholesteryl esters. EPA-containing lipids which were investigated were [A], 1,2,3-trieicosapentaenoyl-glycerol, [B] 2-eicosapentaenoyl-phosphatidylcholine and [C] ethyl ester of EPA. An adjusted amount of lipids [A], [B] and [C] was administered to rats through a gastric tube for 4 days (the first experiment) or for 10 days (the second experiment), and the fatty acid composition of plasma phospholipids and cholesteryl esters was determined. In the first experiment, there were no significant differences in the efficiency for increasing EPA levels in either phospholipids or cholesteryl esters among the lipids. In the second experiment, the EPA levels of both plasma phospholipids and cholesteryl esters of rats administered ethyl ester of EPA were significantly higher than those of rats administered 2-eicosapentaenoyl-phosphatidylcholine. The EPA levels of the rats administered 1,2,3-trieicosapentaenoylglycerol were between the levels of the two groups mentioned above, but the differences in the EPA levels were not significant. Although an ethyl ester-type molecule is not a naturally occurring lipid, ethyl ester of EPA is equal to 1,2,3-trieicosapentaenoyl-glycerol and appears to be superior to 2-eicosapentaenoyl-phosphatidylcholine as to the efficiency for increasing EPA levels in total plasma phospholipids and plasma cholesteryl esters.     

Leaching test of gamma-emitting Cs,Ru, Zr,and U from neutron-irradiated UO2/ZrO2 solid solutions in non-filtered surface seawater

The leaching behaviors of gamma-ray radionuclides, Cs-137, Ru-103, and Zr-95, produced by neutron irradiation of UO₂/ZrO₂ solid solutions, in real surface seawater were investigated under atmospheric conditions. The fraction of radionuclide inventory leached in the seawater was in the order of Cs > Ru (～U) ? Zr, indicating that the fraction was significantly affected by the chemical state of the radionuclides. However, the amount of soluble nuclides was proportional to that of uranium regardless of whether the solid solutions were prepared under an oxidative or reductive environment. A tiny fraction of Ru was filtered out by a 3 kDa nominal molecular weight cut-off filter after the 160 d leaching test, suggesting a different behavior from its ionic form, but Cs and U did not form a colloid-like species in seawater.     

Synthesis of Cubic Boron Nitride from Boron Nitride Synthesized by Pressure Pyrolysis of Borazine

Cubic BN was synthesized under high-temperature and -pressure conditions from BN powder formed by pressure pyrolysis of borazine below 700°C and 100 MPa. The conversion of BN powder to cubic BN was strongly influenced by the residual hydrogen identified by the BH/BN ratio of IR absorption band. The activation energy for cubic BN synthesis from BN powder-20 mol% AIN was 46 kJ/mol, when the starting BN was synthesized at 250°C. A mixture of BN powder and cubic BN particles was converted to cubic BN in a 100% yield by heat treatment at 1800°C and 6.5 GPa without any catalyst. The presence of cubic BN particles does enhance the conversion to cubic BN from BN powder. The energy required for the transformation of starting BN to cubic BN in the presence of cubic BN seed was 355 kJ/mol.     

日本彩色聚乙烯涂覆钢管的开发

试验了彩色聚乙烯涂覆钢管的耐腐蚀性和耐气候性，由于聚乙烯涂层隔绝水的作用，聚乙烯涂覆钢管具有优良的耐腐蚀性能，电阻绝缘值和优良的机械性能。建立了一个新的方式去研究分析聚乙烯抗老化剂消耗和在聚乙烯中的扩散。用有效测定的方法定量地预测彩色聚乙烯涂覆层的寿命，应用这些分析结果，不仅可使新的有色聚乙烯涂覆钢管在恶劣腐蚀环境介质情况下具有高的耐腐蚀性，而且有长的耐气候性。     

Radiation-induced graft copolymerization of butadiene on polyethylene by trapped radicals

The low-temperature grafting of butadiene on polyethylene (PE) preirradiated in air is compared with that on PE preirradiated in vacuo for the effect of several factors on the grafting. Little fundamental difference between the two cases was observed. In both cases the graft conversion curve is trapped radical type and the overall activation energies are 9.7 and 8.4 kcal/mol for 0.947-density PE and 0.916-density PE, respectively. Percent grafting is proportional to the square root of the dose rate (= total dose). The retarding effect of oxygen at irradiation or storage after irradiation on the grafting scarcely appears when the irradiation temperature or storage temperature is below 15°C. For thinner film and lower density of PE this effect appears clearly at the higher temperature. Therefore, it may be concluded that the low-temperature grafting of butadiene onto PE preirradiated in air is initiated predominantly by nonoxidized radical (allyl radical) trapped in PE and that the grafting reaction occurs in the semicrystalline part of PE.     

New Class of High-<Emphasis Type="Italic">T</Emphasis><Subscript>C</Subscript> Diluted Ferromagnetic Semiconductors Based on CaO without Transition Metal Elements

We propose new-type ferromagnetic semiconductors based on CaO and K₂S without any transition metal elements. These materials show transparent and half-metallic ferromagnetism if the deep-impurity-band width (W) induced by doping of C, N, Si, or Ge impurities, and the electron-correlation energy (U) satisfy the Stoner’s condition of highly correlated electron system (U>W). Based on our first-principles calculations, we demonstrate that these materials satisfy the Stoner’s condition, and could be new candidates for transparent and half-metallic DMSs.     

Some properties of mullite powders prepared by chemical vapour deposition

The sinterability of mullite (3Al₂O₃·2SiO₂) powder prepared by chemical vapour deposition was examined to improve the conditions for fabricating dense mullite ceramics. The starting powder contained not only mullite, but also a small amount of -Al₂O₃ (Al-Si spinel) and amorphous material. Although the compressed powder was fired at a temperature between 1550 and 1700 °C for 1, 3 and 5 h, the relative densities of the sintered compacts were limited to 90%: (i) due to the creation of pores/microcracks during the solid state reaction (1100–1350 °C), and (ii) due to restriction on the rearrangement of grains because the amount of liquid phase (1550–1700 °C) was insufficient. Calcination of the starting powder was effective for preparation of easily sinterable powder with homogeneous composition. When the compact formed by compressing the calcined powder at 1400 °C for 1 h was fired at 1650 °C for 3 h, the relative density was raised up to 97.2%; moreover, mullite was the only phase detected from the sintered compact. The sintered compact was composed of polyhedral grains with sizes of 1–2 m and elongated grains with long axes of 6 m.