Optimization study on sample pretreatment of spent fuel storage rack

In order to evaluate radionuclide inventories as an essential item for the permanent disposal of spent fuel storage racks, chemical conditions for a sample pretreatment of a spent fuel storage rack were studied. Especially, the surface microstructure and the radionuclide distributions for the spent fuel storage rack were investigated by using a SEM–EDX and γ-spectrometer for minimizing the matrix effect which could affect a chemical separation process of some β-emitting radionuclides. The samples were pretreated with a mixed solution of 5 M HCl and 2 M HNO₃ by an ultrasonic surface leaching method. Some radionuclides in the raw racks showed the radioactivity of 10²–10³ Bq for about 10 g of sample weight. From the sample pretreatment, it was confirmed that almost all radionuclides in the rack were completely extracted from the rack when the dissolved thickness of the rack became a maximum 15 μm by the ultrasonic surface leaching method. The established pretreatment method was applied for all spent fuel storage rack generated from Korean NPPs to determine the scaling factor. The radioactivities of ⁶⁰Co and ¹³⁷Cs radionuclides in the pretreated solutions were in the range of 4.9E−1~1.5E+2 and 1.2E−1~9.0E+0 Bq/g, respectively.     

Reversible changes between bipolar and unipolar resistance-switching phenomena in a Pt/SrTiOx/Pt cell

We find that resistance switching (RS) phenomena change reversibly between bipolar RS (BRS) and unipolar RS (URS) in a Pt/SrTiO_x/Pt cell. For an asymmetric electrode configuration of Ti/SrTiO_x/Pt cells whose top and bottom interfaces are Ohmic and Schottky-like rectifying, we determine that BRS only occurs when a positive voltage is applied to the bottom Pt electrode at the forming process. During the set process of BRS in a Pt/SrTiO_x/Pt cell, O₂ bubbles develop on the top Pt electrode. From the experimental results for a single sample in which both BRS and URS occur, O^2? ion movement and consequent interfacial resistance modification might play an important role in BRS but not URS.     

Properties of the acoustic intensity vector field in a shallow water waveguide

Acoustic intensity is a vector quantity described by collocated measurements of acoustic pressure and particle velocity. In an ocean waveguide, the interaction among multipath arrivals of propagating wavefronts manifests unique behavior in the acoustic intensity. The instantaneous intensity, or energy flux, contains two components: a propagating and non-propagating energy flux. The instantaneous intensity is described by the time-dependent complex intensity, where the propagating and non-propagating energy fluxes are modulated by the active and reactive intensity envelopes, respectively. Properties of complex intensity are observed in data collected on a vertical line array during the transverse acoustic variability experiment (TAVEX) that took place in August of 2008, 17 km northeast of the Ieodo ocean research station in the East China Sea, 63 m depth. Parabolic equation (PE) simulations of the TAVEX waveguide supplement the experimental data set and provide a detailed analysis of the spatial structure of the complex intensity. A normalized intensity quantity, the pressure-intensity index, is used to describe features of the complex intensity which have a functional relationship between range and frequency, related to the waveguide invariant. The waveguide invariant is used to describe the spatial structure of intensity in the TAVEX waveguide using data taken at discrete ranges.     

The role of tonicity responsive enhancer sites in the transcriptional regulation of human hsp70-2 in response to hypertonic stress

The inducible 70 kDa heat shock proteins (Hsp70) in mice are encoded by two almost identical genes, hsp70.1 and hsp70.3. Studies have found that only hsp70.1 is induced by hypertonic stress while both hsp70.1 and hsp70.3 genes are expressed in response to heat shock stress. It is unclear if the human counterparts, hsp70-2 and hsp70-1, are differentially regulated by heat shock and osmotic stress. This study found that only hsp70-2 was induced by hypertonic stress in human embryonic kidney epithelial cells and fibroblasts, while heat shock stress induced both hsp70-1 and hsp70-2. The human hsp70-2 promoter region contains three TonE (tonicity-responsive enhancer) sites, which were reported to play an important role in the response to hypertonicity. When the reporter plasmids containing different parts of the 5' flanking region of hsp70-2 were transfected into human embryonic kidney epithelial cells or fibroblasts, one TonE site at -135 was found to play a key role in the response to hypertonicity. The inactivation of the TonE site using site-directed mutagenesis led to the complete loss of induction by hypertonicity, which demonstrates the essential role of the TonE site. This suggests that the TonE site and the TonEBP (TonE binding protein) are the major regulators for the cellular response against high osmolarity in human kidney tissue.     

High-frequency magnetic properties of soft magnetic cores based on nanocrystalline alloy powder prepared by thermal oxidation

FeSiBNbCu nanocrystalline alloy powder was thermally oxidized in an air atmosphere to enhance an oxide layer formation on the surface of the powder and subsequently toroidal shape FeSiBNbCu nanocrystalline alloy powder cores were prepared by compaction at room temperature. The phase change on the surface of FeSiBNbCu nanocrystalline alloy powder by thermal oxidation was analyzed and its effect on the high frequency magnetic properties of the compacted cores was investigated. By thermal oxidation, the formation of the oxide layer consisting of Fe₂O₃, CuO, and SiO₂ on the surface of FeSiBNbCu nanocrystalline alloy powder was enhanced and the thickness of oxide layer could be controlled by changing the thermal oxidation time. FeSiBNbCu nanocrystalline alloy powder core prepared from the powder treated by thermal oxidation exhibits a stable permeability up to high frequency range over 10 MHz. The core loss could be reduced remarkably and the dc-bias property could be improved significantly, which were due to the formation of oxide layer consisting of Fe₂O₃, CuO, and SiO₂ on the FeSiBNbCu nanocrystalline alloy powder. The improvement in high-frequency magnetic properties of the FeSiBNbCu nanocrystalline alloy powder cores could be attributed to the effective electrical insulation by oxide layer between the FeSiBNbCu nanocrystalline alloy powders.     

A neutron induced prompt gamma-ray spectroscopy system using a 252Cf neutron source for quantitative analysis of aqueous samples

A neutron induced prompt γ -ray spectrometry (NIPS) facility has been developed at the Nuclear Chemistry Research Division, of the Korea Atomic Energy Research Institute (KAERI) with the aim of analyzing the major components of various elements in aqueous samples. The facility is equipped with a ²⁵²Cf neutron source and a γ-γ coincidence setup with two n-type coaxial HPGe detectors based on NIM spectrometric modules in association with data acquisition and spectral analysis systems. The development of the system, its set-up and the calibration of detection efficiency up to 8 MeV using a set of radionuclides and the (n,γ) reactions of chlorine are described in the paper. This revised version was published online in July 2006 with corrections to the Cover Date.     

Quantitation and pharmacokinetics of 1,4‐diamino‐2,3‐dicyano‐1,4‐bis (2‐aminophenylthio) butadiene (U0126) in rat plasma by liquid chromatography‐tandem mass spectrometry

A simple, robust, and rapid LC‐MS/MS method was developed for the quantitation of U0126 and validated in rat plasma. Plasma samples (20 μL) were deproteinized using 200 μL ACN containing 30 ng/mL of chlorpropamide, internal standard. Chromatographic separation performed on an Agilent Poroshell 120 EC‐C₁₈ column (4.6 × 50 mm, 2.7 μm particle size) with an isocratic mobile phase consisting of a 70:30 v/v mixture of ACN and 0.1% aqueous formic acid. Each sample was run at 0.6 mL/min for a total run time of 2 min per sample. Detection and quantification were performed using a mass spectrometer in selected reaction‐monitoring mode with positive ESI at m/z 381 → 123.9 for U0126 and m/z 277 → 175 for the internal standard. The standard curve was linear over a concentration range of 20–5000 ng/mL with correlation coefficients greater than 0.9965. Precision, both intra‐ and interday, was less than 10.1% with an accuracy of 90.7–99.4%. No matrix effects were observed. U0126 in rat plasma degraded approximately 41.3% after 3‐h storage at room temperature. To prevent degradation, sample handling should be on an ice bath and all solutions kept at 4°C. This method was successfully applied to a pharmacokinetic study of U0126 at various doses in rats.     

Hydrogen exchange study on the hydroxyl groups of serine and threonine residues in proteins and structure refinement using NOE restraints with polar side-chain groups

We recently developed new NMR methods for monitoring the hydrogen exchange rates of tyrosine hydroxyl (Tyr-OH) and cysteine sulfhydryl (Cys-SH) groups in proteins. These methods facilitate the identification of slowly exchanging polar side-chain protons in proteins, which serve as sources of NOE restraints for protein structure refinement. Here, we have extended the methods for monitoring the hydrogen exchange rates of the OH groups of serine (Ser) and threonine (Thr) residues in an 18.2 kDa protein, EPPIb, and thus demonstrated the usefulness of NOE restraints with slowly exchanging OH protons for refining the protein structure. The slowly exchanging Ser/Thr-OH groups were readily identified by monitoring the (13)C(β)-NMR signals in an H(2)O/D(2)O (1:1) mixture, for the protein containing Ser/Thr residues with (13)C, (2)H-double labels at their β carbons. Under these circumstances, the OH groups exist in equilibrium between the protonated and deuterated isotopomers, and the (13)C(β) peaks of the two species are resolved when their exchange rate is slower than the time scale of the isotope shift effect. In the case of EPPIb dissolved in 50 mM sodium phosphate buffer (pH 7.5) at 40 °C, one Ser and four Thr residues were found to have slowly exchanging hydroxyl groups (k(ex) < ~40 s(-1)). With the information for the slowly exchanging Ser/Thr-OH groups in hand, we could collect additional NOE restraints for EPPIb, thereby making a unique and important contribution toward defining the spatial positions of the OH protons, and thus the hydrogen-bonding acceptor atoms.