Radiochemical analysis of rubble and trees collected from Fukushima Daiichi Nuclear Power Station

To characterize the rubble and trees contaminated by radionuclides released by the recent accident at the Fukushima Daiichi Nuclear Power Station, the radiochemical analysis protocols were modified using those developed by the Japan Atomic Energy Agency for the waste generated by research, industrial, and medical facilities. The radioactivity concentrations of gamma-ray-emitting nuclides ⁶⁰Co, ⁹⁴Nb, ¹⁵²Eu, and ¹⁵⁴Eu, and beta-particle-emitting nuclides ¹⁴C, ¹²⁹I, ³⁶Cl, ⁷⁹Se, and ⁹⁹Tc were successfully applied by the modified analytical method. In contrast, the radioactivity concentrations of ³H, ⁹⁰Sr, ¹³⁷Cs, and alpha-particle-emitting nuclides were applied by the conventional method. Unfortunately, ³⁶Cl, ⁹⁴Nb, ¹²⁹I, ¹⁵²Eu, ¹⁵⁴Eu, and alpha-particle-emitting nuclides were below the detection limit of the conventional method. The measured radioactivity concentrations, except for that of ³H, were not uniform in the area but depended on the reactor unit. Although the radioactivity concentrations were varied widely, this analysis successfully clarified the characteristics of the radioactivity concentrations of the rubble and trees.     

Chemical speciation of arsenic-accumulating mineral in a sedimentary iron deposit by synchrotron radiation multiple X-ray analytical techniques

The comprehensive characterization of As(V)-bearing iron minerals from the Gunma iron deposit, which were probably formed by biomineralization, was carried out by utilizing multiple synchrotron radiation (SR)-based analytical techniques at BL37XU at SPring-8. SR microbeam X-ray fluorescence (SR-mu-XRF) imaging showed a high level of arsenic accumulation in the iron ore as dots of ca. 20 microm. Based on SEM observations and SR X-ray powder diffraction (SR-XRD) analysis, it was found that arsenic is selectively accumulated in strengite (FePO4 x 2H2O) with a concentric morphology, which may be produced by a biologically induced process. Furthermore, the X-ray absorption fine structure (XAFS) analysis showed that arsenic in strengite exists in the arsenate (AsO4(3-)) form and is coordinated by four oxygen atoms at 1.68 angstroms. The results suggest that strengite accumulates arsenic by isomorphous substitution of AsO4(3-) for PO4(3-) to form a partial solid-solution of strengite and scorodite (FeAsO4 x 2H2O). The specific correlation between the distribution of As and biominerals indicates that microorganisms seems to play an important role in the mineralization of strengite in combination with an arsenic-accumulating process.     

High precision chemical mechanical polishing of highly-boron-doped Si wafer used for epitaxial substrate

The surface waviness with concentric circular pattern is generated on highly-boron-doped Si wafer by chemical–mechanical polishing (CMP) with amine system polishing slurry. To investigate the generation mechanism of the waviness, the mechanical and chemical characteristics were clarified using the silicon crystal samples with various boron concentration level ranging from 2.9 × 10¹⁷ cm⁻³ to 1.3 × 10²⁰ cm⁻³. The conventional silicon substrate used as epitaxial wafer has boron concentration of about 2.5 × 10¹⁸ cm⁻³, a region at which the radical change of etching rate is induced with amine system chemical reagent. The mechanical micro-hardness of highly-boron-doped Si is 30% higher than that of lightly-doped Si. It is found that SiB bond in crystal lattice is firmed up and stabilized for mechanical stress and chemical reaction. To cancel the difference in CMP rate based on boron concentration deviation, increasing the mechanical action in CMP was proposed and performed. The precision CMP was performed using the harder polishing pad and a smooth surface without waviness was obtained.     

Nonlinear Ultrasound Propagation in Solid $$^4\hbox {He}$$ Compared with Shear Modulus Experiments

Ultrasound attenuation (\(\alpha \)) and velocity (V) at 9.6 MHz are measured in polycrystalline hcp \(^4\hbox {He}\). The ultrasound signal above 200 mK is linear and understood in terms of resonant vibration of dislocation segments pinned between network nodes with an average pinning length of 3.7 \(\mu \hbox {m}\), much shorter than 59 \(\mu \hbox {m}\) estimated from a shear modulus measurement. Dramatic changes in \(\alpha \) and V are observed below 200 mK. The changes are strongly dependent on temperature and are nonlinear and hysteretic. These effects result from pinning of dislocations by \(^3\hbox {He}\) impurities (nominal concentration of 0.3 ppm). The dislocation damping constant due to thermal phonons, the binding energy between dislocation and \(^3\hbox {He}\), and the average network pinning length obtained from the ultrasound data are compared with those from the shear modulus experiments.     

Determination of various constituent elements of polyethylene terephthalate bottles used for beverages in Japan

Polyethylene terephthalate (PET) bottles are some of the most commonly used containers for beverages. During the manufacturing process of PET resin in Japan, metallic catalysts such as Sb and Ge are widely used, with other metals or metallic compounds also being employed to improve the quality of PET bottles. However, few reports into the contents of such elements exist. Thus, we herein report the concentrations of 34 elements (ie, Li, B, Na, Mg, Al, P, K, Ca, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Ga, Ge, As, Se, Rb, Sr, Zr, Mo, Ag, Cd, Sn, Sb, Cs, Ba, W, Pb, and U) in 16 samples of unused virgin PET bottles for beverages. The measurement was performed by inductively coupled plasma optical emission spectrometry (ICP-OES) and inductively coupled plasma mass spectrometry (ICP-MS), and these bottles were found to contain five main elements (ie, <0.5- to 50-mg/kg Ge, <1- to 26-mg/kg Ti, <0.1- to 279-mg/kg Sb, <10- to 48-mg/kg P, and <0.5- to 53-mg/kg Co) that were used as polymerisation catalysts, stabilisers, oxidation catalysts, and bluing agents. Furthermore, when these residual element concentrations in 21 commercial mineral-water PET bottles were determined, there was no significant difference from unused bottles.     

Synthesis of LiNi1−xCoxPO4/C nanocomposite cathode for lithium ion batteries by a combination of aerosol and powder technologies

Pure LiNi_1?xCo_xPO₄ (x?=?0, 0.2, 0.5, 0.8, 1) was synthesized by spray pyrolysis followed by heat treatment. The X-ray diffraction (XRD) patterns of LiNi_1?xCo_xPO₄ were indexed to olivine structure with a Pnma space group. The peak shift and variation of lattice parameters suggested that LiNi_1?xCo_xPO₄ solid solution was formed. Moreover, LiNi_1?xCo_xPO₄/C (x?=?0, 0.2, 0.5, 0.8, 1) nanocomposites were successfully synthesized by a combination of spray pyrolysis and wet ball milling followed by heat treatment. The XRD patterns of all samples were indexed to olivine structure with a Pnma space group. From scanning electron microscopy images, the primary particle sizes of LiNi_1?xCo_xPO₄/C nanocomposites were reduced to the range of approximately 50–100?nm. LiNi_0.5Co_0.5PO₄/C cathode exhibited a higher first discharge capacity and cyclability than those of pure LiNi_0.5Co_0.5PO₄. Cyclic voltammetry data demonstrated that reduction peaks of LiNi_0.5Co_0.5PO₄/C cathode occur at 4.44?V and 4.71?V, which were ascribed to Co³⁺/Co²⁺ and Ni³⁺/Ni²⁺ reduction couples, respectively. Electrochemical impedance spectroscopy data revealed that the LiNi_0.5Co_0.5PO₄/C cathode had a smaller charge transfer resistance, resulting in a faster redox reaction kinetics for the lithium insertion and extraction, due to reduced particle size and introduced conductive carbon.     

Zirconia Coating on Stainless Steel Sheets from Organozirconium Compounds

The stability and the coating characteristics of a variety of organozirconium compounds have been investigated to coat ZrO₂ films on stainless steets for the improvement of heat resistance against oxidation. Zirconium tetraoctylate and zirconium tetrakis(acetylacetonate) were found to be more stable than zirconium alkoxides in an ambient atmosphere. The ZrO₂ films from zirconium alkoxides became white and discontinuous when the thickness of the films exceeded about 200 Å (20 nm). On the other hand, transparent ZrO₂ films were obtained from zirconium tetraoctylate and zirconium tetrakis(acetylacetonate). The IR spectra of the films showed that the heat treatment at 400°C for 5 min produced organic-free ZrO₂ films. The heat resistance of stainless steel sheets against oxidation was improved by the ZrO₂ coating, depending on the film thickness.     

Carboxylated polysulfone membranes having a chiral recognition site induced by an alternative molecular imprinting technique

SUMMARY Molecularly imprinted polymeric membranes were prepared from carboxylated polysulfone. Membranes imprinted by Z-D-Glu recognize the D-isomer in preference to the corresponding L-isomer, and vice versa. The amino acid preferentially adsorbed by the membrane was also selectively permeated by electrodialysis. Received: 22 January 1998/Accepted: 20 February 1998     

Diffusion of low molecular weight siloxane from bulk to surface

Silicone-based materials for outdoor insulators have the advantage that low molecular weight (LMW) components migrate through the material and coat the surface, thereby restoring hydrophobicity over a period of hours. By measuring the IR absorption of siloxane migrating to the silicone surface through a thin carbon coating, the time constant for migration was calculated. According to the time dependence of IR-absorbance, the time constant for migration ranged from 1.6 to 5.3 h depending on alumina trihydrate (ATH) filler concentration