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Sample records for pu allowed solutions

  1. Sonochemical redox reactions of Pu(III) and Pu(IV) in aqueous nitric solutions.

    Science.gov (United States)

    Virot, Matthieu; Venault, Laurent; Moisy, Philippe; Nikitenko, Sergey I

    2015-02-14

    The behavior of Pu(iv) and Pu(iii) was investigated in aqueous nitric solutions under ultrasound irradiation (Ar, 20 kHz). In the absence of anti-nitrous reagents, ultrasound has no effect on Pu(iv), while Pu(iii) can be rapidly oxidized to Pu(iv) due to the autocatalytic formation of HNO(2) induced by HNO(3) sonolysis. In the presence of anti-nitrous reagents (sulfamic acid or hydrazinium nitrate), Pu(iv) can be sonochemically reduced to Pu(iii). The reduction follows a first order reaction law and leads to a steady state where Pu(iv) and Pu(iii) coexist in solution. The reduction process is attributed to the sonochemical generation of H(2)O(2) in solution. The kinetics attributed to the reduction of Pu(iv) are however higher than those related to the formation of H(2)O(2) which, after several hypotheses, is explained by the sonochemical erosion of the titanium-based sonotrode. Titanium particles thereby generated can be solubilized under ultrasound and generate Ti(iii) as an intermediate species, a strong reducing agent able to react with Pu(iv).

  2. Critical experiments with mixed plutonium-uranium nitrate solutions having Pu:(Pu + U) ratios greater than 0.5

    Energy Technology Data Exchange (ETDEWEB)

    Primm, R.T. III [Oak Ridge National Lab., TN (United States); Lloyd, R.C.; Clayton, E.D. [Pacific Northwest Lab., Richland, WA (United States)

    1986-04-01

    A series of critical experiments was conducted with mixed plutonium-uranium nitrate solutions having Pu:(Pu+U) ratios >0.5. Three geometries and four conditions of reflection were examined. The plutonium concentrations ranged from 170 to 350 g/L. The value of k-effective for each experiment was calculated using the KENO-IV code and 27-group cross sections derived from the Evaluated Nuclear Data File B--version IV (ENDF/B-IV). The mean value for the set of 26 experiments was 1.003, with a minimum value of 0.987 and a maximum of 1.022. The spread in the distribution of calculated k-effectives is believed to be the result of uncertainties in analytical chemistry measurements. No correlation between condition of reflection and calculated k-effective was found. An allowable multiplication factor to be used in the evaluation of reprocessing equipment at conditions that have been investigated was calculated to be 0.945.

  3. Electrodeposition of Pu in(NH4)2SO4 Solution

    Institute of Scientific and Technical Information of China (English)

    SUN; Xiao-yi; YANG; Chun-li; MAO; Guo-shu; HUANG; Kun; SUN; Hong-qing; MA; Peng

    2013-01-01

    The yield of eletrodeposition of Pu in ammonium oxalate is high,however the process should be heated and the pH changes too fast to control.To find a way to electroplate Pu with a high yield and easy operation,electro deposition of Pu in ammonium sulfate solution was studied.Firstly,destroy organics introduced in pretreatment with concentrated nitric acid and 30%hydrogen

  4. Improvement of INVS Measurement Uncertainty for Pu and U-Pu Nitrate Solution

    Energy Technology Data Exchange (ETDEWEB)

    Swinhoe, Martyn Thomas [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Menlove, Howard Olsen [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Marlow, Johnna Boulds [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Makino, Risa [Japan Atomic Energy Agency (JAEA), Tokai (Japan); Nakamura, Hironbu [Japan Atomic Energy Agency (JAEA), Tokai (Japan)

    2017-04-27

    In the Tokai Reprocessing Plant (TRP) and the Plutonium Conversion Development Facility (PCDF), a large amount of plutonium nitrate solution which is recovered from light water reactor (LWR) and advanced thermal reactor (ATR), FUGEN are being stored. Since the solution is designated as a direct use material, the periodical inventory verification and flow verification are being conducted by Japan Safeguard Government Office (JSGO) and International Atomic Agency (IAEA).

  5. Redox reactions of Pu(IV) and Pu(III) in the presence of acetohydroxamic acid in HNO(3) solutions.

    Science.gov (United States)

    Tkac, Peter; Precek, Martin; Paulenova, Alena

    2009-12-21

    The reduction of Pu(IV) in the presence of acetohydroxamic acid (HAHA) was monitored by vis-NIR spectroscopy. All experiments were performed under low HAHA/Pu(IV) ratios, where only the Pu(IV)-monoacetohydroxamate complex and Pu uncomplexed with HAHA were present in relevant concentrations. Time dependent concentrations of all absorbing species were resolved using molar extinction coefficients for Pu(IV), Pu(III), and the Pu(AHA)(3+) complex by deconvolution of spectra. From fitting of the experimental data by rate equations integrated by a numeric method three reactions were proposed to describe a mechanism responsible for the reduction and oxidation of plutonium in the presence of HAHA and HNO(3). Decomposition of Pu(AHA)(3+) follows a second order reaction mechanism with respect to its own concentration and leads to the formation of Pu(III). At low HAHA concentrations, a two-electron reduction of uncomplexed Pu(IV) with HAHA also occurs. Formed Pu(III) is unstable and slowly reoxidizes back to Pu(IV), which, at the point when all HAHA is decomposed, can be catalyzed by the presence of nitrous acid.

  6. {sup 239,} {sup 240,} {sup 241}Pu fingerprinting of plutonium in western US soils using ICPMS: solution and laser ablation measurements

    Energy Technology Data Exchange (ETDEWEB)

    Cizdziel, James V. [University of Nevada - Las Vegas, Harry Reid Center for Environmental Studies, Las Vegas, NV (United States); Ketterer, Michael E. [Northern Arizona University, Department of Chemistry and Biochemistry, Box 5698, Flagstaff, AZ (United States); Farmer, Dennis [University of Nevada - Las Vegas, Department of Health Physics, Las Vegas, NV (United States); Faller, Scott H. [US Environmental Protection Agency, Radiation and Indoor Environments National Laboratory, Box 98517, Las Vegas, NV (United States); Hodge, Vernon F. [University of Nevada - Las Vegas, Department of Chemistry, Las Vegas, NV (United States)

    2008-01-15

    Sector field inductively coupled plasma mass spectrometry (SF-ICPMS) has been used with analysis of solution samples and laser ablation (LA) of electrodeposited alpha sources to characterize plutonium activities and atom ratios prevalent in the western USA. A large set of surface soils and attic dusts were previously collected from many locations in the states of Nevada, Utah, Arizona, and Colorado; specific samples were analyzed herein to characterize the relative contributions of stratospheric fallout vs. Nevada Test Site (NTS) plutonium. This study illustrates two different ICPMS-based analytical strategies that are successful in fingerprinting Pu in environmental soils and dusts. Two specific datasets have been generated: (1) soils are leached with HNO{sub 3}-HCl, converted into electrodeposited alpha sources, counted by alpha spectrometry, then re-analyzed using laser ablation SF-ICPMS; (2) samples are completely dissolved by treatment with HNO{sub 3}-HF-H{sub 3}BO{sub 3}, Pu fractions are prepared by extraction chromatography, and analyzed by SF-ICPMS. Optimal laser ablation and ICPMS conditions were determined for the re-analysis of archived alpha spectrometry ''planchette'' sources. The best ablation results were obtained using a large spot size (200 {mu}m), a defocused beam, full repetition rate (20 Hz) and scan rate (200 {mu}m s{sup -1}); LA-ICPMS data were collected with a rapid electrostatic sector scanning experiment. Less than 10% of the electroplated surface area is consumed in the LA-ICPMS analysis, which would allow for multiple re-analyses. Excellent agreement was found between {sup 239+240}Pu activities determined by LA-ICPMS vs. activity results obtained by alpha spectrometry for the same samples ten years earlier. LA-ICPMS atom ratios for {sup 240}Pu/{sup 239}Pu and {sup 241}Pu/{sup 239}Pu range from 0.038-0.132 and 0.00034-0.00168, respectively, and plot along a two-component mixing line ({sup 241}Pu/{sup 239}Pu = 0

  7. Validation of MCNP6.1 for Criticality Safety of Pu-Metal, -Solution, and -Oxide Systems

    Energy Technology Data Exchange (ETDEWEB)

    Kiedrowski, Brian C. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Conlin, Jeremy Lloyd [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Favorite, Jeffrey A. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Kahler, III, Albert C. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Kersting, Alyssa R. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Parsons, Donald K. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Walker, Jessie L. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2014-05-13

    Guidance is offered to the Los Alamos National Laboratory Nuclear Criticality Safety division towards developing an Upper Subcritical Limit (USL) for MCNP6.1 calculations with ENDF/B-VII.1 nuclear data for three classes of problems: Pu-metal, -solution, and -oxide systems. A benchmark suite containing 1,086 benchmarks is prepared, and a sensitivity/uncertainty (S/U) method with a generalized linear least squares (GLLS) data adjustment is used to reject outliers, bringing the total to 959 usable benchmarks. For each class of problem, S/U methods are used to select relevant experimental benchmarks, and the calculational margin is computed using extreme value theory. A portion of the margin of sub criticality is defined considering both a detection limit for errors in codes and data and uncertainty/variability in the nuclear data library. The latter employs S/U methods with a GLLS data adjustment to find representative nuclear data covariances constrained by integral experiments, which are then used to compute uncertainties in keff from nuclear data. The USLs for the classes of problems are as follows: Pu metal, 0.980; Pu solutions, 0.973; dry Pu oxides, 0.978; dilute Pu oxide-water mixes, 0.970; and intermediate-spectrum Pu oxide-water mixes, 0.953.

  8. Reactivity of the uranium (U(IV)/U(VI)) and the plutonium (Pu(III)/Pu(IV)) in nitric aqueous solution under ultrasound; De l'influence des ultrasons sur la reactivite de l'uranium (U(IV)/U(VI)) et du plutonium (PU(III)/PU(IV)) en solution aqueuse nitrique

    Energy Technology Data Exchange (ETDEWEB)

    Venault, L

    1998-07-01

    To minimize the volumes of solid waste and industrial effluents generated at the end of cycle, particularly in the spent nuclear fuel reprocessing industry, research is currently under way on so-called innovative processes, designed to induce chemical reactions without adding reagent to the media. Among these processes, the use of ultrasound can prove advantageous, and the purpose of this study is to assess accurately the potential for its application. In the present context, this work shows that the transmission of an ultrasonic wave in aqueous nitric acid solution leads to: the accumulation of nitrous acid in solution, until a steady-sate concentration is reached; the removal of nitrogen monoxide and nitrogen dioxide in the gas stream. The initial kinetics of the formation of HNO{sub 2} in solution was quantified as a function of the nitric acid concentration and the ultrasound intensity. It was also shown than an excess of nitrous acid in nitric solution decomposes under the effect of ultrasound. It is also possible to accumulate hydrogen peroxide in solution during the ultrasonic irradiation of aqueous nitric acid solutions in the presence of a chemical species (N{sub 2}H{sub 5}{sup +}, NH{sub 2}SO{sub 3}H...) which reacts rapidly with HNO{sub 2}, preventing the reduction of H{sub 2}O{sub 2} by HNO{sub 2}. The mechanisms of HNO{sub 2} formation and decomposition, and the mechanism of H{sub 2}O{sub 2} formation during the ultrasonic irradiation of aqueous nitric acid solutions, are presented. Control of H{sub 2}O{sub 2} or HNO{sub 2} in a nitric acid medium under the effect of an ultrasonic wave can be exploited to control redox reactions of uranium and plutonium ions, particularly with respect to the oxidation of U and Pu (U(IV){yields} U(IV) or Pu(III) {yields} Pu(IV)) and the reduction of Pu (Pu(IV){yields} Pu(III). The redox behavior of uranium and plutonium ions in aqueous nitric solution subject to an ultrasonic flux is interpreted in term of effects

  9. Structural recovery of self-irradiated natural and {sup 238}Pu-doped zircon in an acidic solution at 175 deg. C

    Energy Technology Data Exchange (ETDEWEB)

    Geisler, Thorsten [Institut fuer Mineralogie, University of Muenster, Corrensstrasse 24, 48149 Muenster (Germany)]. E-mail: tgeisler@nwz.uni-muenster.de; Burakov, Boris [Laboratory of Applied Mineralogy and Radiogeochemistry, V.G. Khlopin Radium Institute, 28, 2nd Murinskiy ave., St. Petersburg, 194021 (Russian Federation); Yagovkina, Maria [Laboratory of Applied Mineralogy and Radiogeochemistry, V.G. Khlopin Radium Institute, 28, 2nd Murinskiy ave., St. Petersburg, 194021 (Russian Federation); Garbuzov, Vladimir [Laboratory of Applied Mineralogy and Radiogeochemistry, V.G. Khlopin Radium Institute, 28, 2nd Murinskiy ave., St. Petersburg, 194021 (Russian Federation); Zamoryanskaya, Maria [Laboratory of Applied Mineralogy and Radiogeochemistry, V.G. Khlopin Radium Institute, 28, 2nd Murinskiy ave., St. Petersburg, 194021 (Russian Federation); Zirlin, Vladimir [Laboratory of Applied Mineralogy and Radiogeochemistry, V.G. Khlopin Radium Institute, 28, 2nd Murinskiy ave., St. Petersburg, 194021 (Russian Federation); Nikolaeva, Larisa [Laboratory of Applied Mineralogy and Radiogeochemistry, V.G. Khlopin Radium Institute, 28, 2nd Murinskiy ave., St. Petersburg, 194021 (Russian Federation)

    2005-01-01

    We have investigated the aqueous stability of self-irradiated natural and synthetic {sup 238}Pu-doped zircon (4.7 wt% of {sup 238}Pu) in an acidic solution at 175 deg. C. Both zircon samples have suffered a similar deg.ree of self-irradiation damage, as given by their deg.ree of amorphization. X-ray diffraction measurements revealed that during the hydrothermal treatment only the disordered crystalline remnants recovered in the natural zircon, whereas in the {sup 238}Pu-doped zircon the amorphous phase strongly recrystallized. Such a different alteration behavior of natural and Pu-doped zircon is discussed in terms of two fundamentally different alteration mechanisms. Our results demonstrate that further experimental studies with Pu-doped zircon are required before any reliable prediction about the long-term aqueous stability of an actinide waste form based on zircon can be made.

  10. Accelerator Mass Spectrometry of Actinides in Ground- and Seawater: An Innovative Method Allowing for the Simultaneous Analysis of U, Np, Pu, Am, and Cm Isotopes below ppq Levels.

    Science.gov (United States)

    Quinto, Francesca; Golser, Robin; Lagos, Markus; Plaschke, Markus; Schäfer, Thorsten; Steier, Peter; Geckeis, Horst

    2015-06-02

    (236)U, (237)Np, and Pu isotopes and (243)Am were determined in ground- and seawater samples at levels below ppq (fg/g) with a maximum sample size of 250 g. Such high sensitivity was possible by using accelerator mass spectrometry (AMS) at the Vienna Environmental Research Accelerator (VERA) with extreme selectivity and recently improved efficiency and a significantly simplified separation chemistry. The use of nonisotopic tracers was investigated in order to allow for the determination of (237)Np and (243)Am, for which isotopic tracers either are rarely available or suffer from various isobaric mass interferences. In the present study, actinides were concentrated from the sample matrix via iron hydroxide coprecipitation and measured sequentially without previous chemical separation from each other. The analytical method was validated by the analysis of the Reference Material IAEA 443 and was applied to groundwater samples from the Colloid Formation and Migration (CFM) project at the deep underground rock laboratory of the Grimsel Test Site (GTS) and to natural water samples affected solely by global fallout. While the precision of the presented analytical method is somewhat limited by the use of nonisotopic spikes, the sensitivity allows for the determination of ∼10(5) atoms in a sample. This provides, e.g., the capability to study the long-term release and retention of actinide tracers in field experiments as well as the transport of actinides in a variety of environmental systems by tracing contamination from global fallout.

  11. Analytical Instrument of X-ray Fluorescence Determine Concentration of U and Pu in Organic Solution at the Same Time

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    An instrument is developed to measure the concentration of U, Pu and the intensity of gamma ray in samples of 1AP organic phase at the same time. The Ag cold cathode is used to excite L series X-ray fluorescence of U and Pu. The Si-pin detector is

  12. Study and Application of Closed HOPG Diffractive EDXRF in Research of Pu Purification

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    <正>In the Pu purification research, the recovering of Pu is very important. So the Pu concentration in the tail solution must be strictly controlled to several μg/mL. To determine Pu concentration in the tail

  13. RAPID DETERMINATION OF 237 NP AND PU ISOTOPES IN WATER BY INDUCTIVELY COUPLED PLASMA MASS SPECTROMETRY AND ALPHA SPECTROMETRY

    Energy Technology Data Exchange (ETDEWEB)

    Maxwell, S.; Jones, V.; Culligan, B.; Nichols, S.; Noyes, G.

    2010-06-23

    A new method that allows rapid preconcentration and separation of plutonium and neptunium in water samples was developed for the measurement of {sup 237}Np and Pu isotopes by inductively-coupled plasma mass spectrometry (ICP-MS) and alpha spectrometry; a hybrid approach. {sup 238}U can interfere with {sup 239}Pu measurement by ICP-MS as {sup 238}UH{sup +} mass overlap and {sup 237}Np via peak tailing. The method provide enhanced removal of uranium by separating Pu and Np initially on TEVA Resin, then moving Pu to DGA resin for additional removal of uranium. The decontamination factor for uranium from Pu is almost 100,000 and the decontamination factor for U from Np is greater than 10,000. This method uses stacked extraction chromatography cartridges and vacuum box technology to facilitate rapid separations. Preconcentration is performed using a streamlined calcium phosphate precipitation method. Purified solutions are split between ICP-MS and alpha spectrometry so that long and short-lived Pu isotopes can be measured successfully. The method allows for simultaneous extraction of 20 samples (including QC samples) in 4 to 6 hours, and can also be used for emergency response. {sup 239}Pu, {sup 242}Pu and {sup 237}Np were measured by ICP-MS, while {sup 236}Pu, {sup 238}Pu, and {sup 239}Pu were measured by alpha spectrometry.

  14. Designing Pu600 for Authentication

    Energy Technology Data Exchange (ETDEWEB)

    White, G

    2008-07-10

    Many recent Non-proliferation and Arms Control software projects include an authentication component. Demonstrating assurance that software and hardware performs as expected without hidden 'back-doors' is crucial to a project's success. In this context, 'authentication' is defined as determining that the system performs only its intended purpose and performs that purpose correctly and reliably over many years. Pu600 is a mature software solution for determining the presence of Pu and the ratio of Pu240 to Pu239 by analyzing the gamma ray spectra in the 600 KeV region. The project's goals are to explore hardware and software technologies which can by applied to Pu600 which ease the authentication of a complete, end-to-end solution. We will discuss alternatives and give the current status of our work.

  15. (1-xPux)Sb solid solutions. 1. Magnetic configurations

    DEFF Research Database (Denmark)

    Normile, P.S.; Stirling, W.G.; Mannix, D.

    2002-01-01

    are triple k (as in x=0, USb), but that the x=0.75 sample is initially (at T-N) triple k, but at a lower temperature of T' starts to transform to a single-k configuration (as found in x=1, PuSb). The (H, T) phase diagram of this sample is presented. At T=10 K some 30% of the x=0.75 sample remains...

  16. The general form of the coupled Horndeski Lagrangian that allows cosmological scaling solutions

    CERN Document Server

    Gomes, Adalto R

    2015-01-01

    We consider the general scalar field Horndeski Lagrangian coupled to matter. Within this class of models, we present two results that are independent of the particular form of the model. First, we show that in a Friedmann-Robertson-Walker metric the Horndeski Lagrangian coincides with the pressure of the scalar field. Second, we employ the previous result to identify the most general form of the Lagrangian that allows for cosmological scaling solutions, i.e. solutions where the ratio of matter to field density and the equation of state remain constant. Scaling solutions of this kind may help solving the coincidence problem since in this case the presently observed ratio of matter to dark energy does not depend on initial conditions, but rather on the theoretical parameters.

  17. Stability of DMHAN on 238Pu α-Radiolysis

    Institute of Scientific and Technical Information of China (English)

    WANG; Liang; HE; Hui; SONG; Peng

    2013-01-01

    238Pu was used asαliquid inside source(does rate:34.0 Gy·g-1·min-1)for the radiolysis of N,N-dimethylhydroxylamine(DMHAN).DMHAN can reduce Pu(Ⅳ)efficiently,in nitric acid solution,Pu should be trivalence while DMHAN exists.Characteristic wavelength of Pu(Ⅲ)and Pu(Ⅳ)in radiolysis

  18. Isotope dilution gamma spectrometry for Pu using low energy photons

    Energy Technology Data Exchange (ETDEWEB)

    Paul, S.; Sarkar, A.; Alamelu, D.; Shah, R.V.; Aggarwal, S.K. [Bhabha Atomic Reseach Centre, Mumbai (India). Fuel Chemistry Div.

    2012-07-01

    Isotope dilution gamma spectrometry (IDGS) for determination of the Pu concentration, using high resolution gamma-ray spectrometry (HRGS) in the 40-150 keV energy range, is developed and described. The methodology involves purification of Pu by an anion exchange procedure, followed by the determination of Pu isotopic composition using HRGS. For isotope dilution, a pre-calibrated power reactor grade Pu ({proportional_to} 70 at. % {sup 239}Pu) solution from an Indian PHWR was used as a spike for research reactor grade Pu ({proportional_to} 95 at. % {sup 239}Pu) samples and vice versa. Changes in {sup 240}Pu/{sup 239}Pu (45.24 keV/51.62 keV) and {sup 241}Pu/{sup 239}Pu (148.57 keV/129.29 keV) activity ratios in the spiked samples were determined by gamma spectrometry. Using the atom ratios calculated from the measured activity ratios, the concentration of Pu in the sample was calculated using two different efficiency calibration methods. The isotopic composition and concentration of Pu samples both from power reactor and research reactor grade agreed well with the values obtained by isotope dilution-thermal ionization mass spectrometry. The present method also shows the superiority of using the {sup 240}Pu/{sup 239}Pu atom ratio against the {sup 241}Pu/{sup 239}Pu atom ratio in IDGS with respect to the accuracy and precision. (orig.)

  19. Controls on Soluble Pu Concentrations in PuO2/Magnetite Suspensions

    Energy Technology Data Exchange (ETDEWEB)

    Felmy, Andrew R.; Moore, Dean A.; Pearce, Carolyn I.; Conradson, Steven D.; Qafoku, Odeta; Buck, Edgar C.; Rosso, Kevin M.; Ilton, Eugene S.

    2012-11-06

    Time-dependent reduction of PuO2(am) was studied over a range of pH values in the presence of aqueous Fe(II) and magnetite (Fe3O4) nanoparticles. At early time frames (up to 56 days) very little aqueous Pu was mobilized from PuO2(am), even though measured pH and redox potentials, coupled to equilibrium thermodynamic modeling indicated the potential for significant reduction of PuO2(am) to relatively soluble Pu(III). Introduction of Eu(III) or Nd(III) to the suspensions as competitive cations to displace possible sorbed Pu(III) resulted in the release of significant concentrations of aqueous Pu. However, the similarity of aqueous Pu concentrations that resulted from the introduction of Eu(III)/Nd(III) to suspensions with and without magnetite indicated that the Pu was displaced from the PuO2(am), not from magnetite. The fact that soluble forms of Pu can be displaced from the surface of PuO2(am) represents a potential, but previously unidentified, source of Pu to aqueous solution or subsurface groundwaters.

  20. Pu Anion Exchange Process Intensification

    Energy Technology Data Exchange (ETDEWEB)

    Taylor-Pashow, K. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

    2015-10-08

    This project seeks to improve the efficiency of the plutonium anion-exchange process for purifying Pu through the development of alternate ion-exchange media. The objective of the project in FY15 was to develop and test a porous foam monolith material that could serve as a replacement for the current anion-exchange resin, Reillex® HPQ, used at the Savannah River Site (SRS) for purifying Pu. The new material provides advantages in efficiency over the current resin by the elimination of diffusive mass transport through large granular resin beads. By replacing the large resin beads with a porous foam there is much more efficient contact between the Pu solution and the anion-exchange sites present on the material. Several samples of a polystyrene based foam grafted with poly(4-vinylpyridine) were prepared and the Pu sorption was tested in batch contact tests.

  1. Program Pu Futures 2006

    Energy Technology Data Exchange (ETDEWEB)

    Fluss, M

    2006-06-12

    The coordination chemistry of plutonium remains relatively unexplored. Thus, the fundamental coordination chemistry of plutonium is being studied using simple multi-dentate ligands with the intention that the information gleaned from these studies may be used in the future to develop plutonium-specific sequestering agents. Towards this goal, hard Lewis-base donors are used as model ligands. Maltol, an inexpensive natural product used in the commercial food industry, is an ideal ligand because it is an all-oxygen bidentate donor, has a rigid structure, and is of small enough size to impose little steric strain, allowing the coordination preferences of plutonium to be the deciding geometric factor. Additionally, maltol is the synthetic precursor of 3,4-HOPO, a siderophore-inspired bidentate moiety tested by us previously as a possible sequestering agent for plutonium under acidic conditions. As comparisons to the plutonium structure, Ce(IV) complexes of the same and related ligands were examined as well. Cerium(IV) complexes serve as good models for plutonium(IV) structures because Ce(IV) has the same ionic radius as Pu(IV) (0.94 {angstrom}). Plutonium(IV) maltol crystals were grown out of a methanol/water solution by slow evaporation to afford red crystals that were evaluated at the Advanced Light Source at Lawrence Berkeley National Laboratory using single crystal X-ray diffraction. Cerium(IV) complexes with maltol and bromomaltol were crystallized via slow evaporation of the mother liquor to afford tetragonal, black crystals. All three complexes crystallize in space group I4{sub 1}/a. The Ce(IV) complex is isostructural with the Pu(IV) complex, in which donating oxygens adopt a trigonal dodecahedral geometry around the metal with the maltol rings parallel to the crystallographic S{sub 4} axis and lying in a non-crystallographic mirror plane of D{sub 2d} molecular symmetry (Fig 1). The metal-oxygen bonds in both maltol complexes are equal to within 0.04 {angstrom

  2. Extinct 244Pu in Ancient Zircons

    Science.gov (United States)

    Turner, Grenville; Harrison, T. Mark; Holland, Greg; Mojzsis, Stephen J.; Gilmour, Jamie

    2004-10-01

    We have found evidence, in the form of fissiogenic xenon isotopes, for in situ decay of 244Pu in individual 4.1- to 4.2-billion-year-old zircons from the Jack Hills region of Western Australia. Because of its short half-life, 82 million years, 244Pu was extinct within 600 million years of Earth's formation. Detrital zircons are the only known relics to have survived from this period, and a study of their Pu geochemistry will allow us to date ancient metamorphic events and determine the terrestrial Pu/U ratio for comparison with the solar ratio.

  3. Liquid chromatographic studies on the behaviour of Pu(III), Pu(IV) and Pu(VI) on a RP stationary phase in presence of α-hydroxyisobutyric acid as a chelating agent

    Energy Technology Data Exchange (ETDEWEB)

    Jaison, P.G.; Kumar, Pranaw; Telmore, Vijay M. [Bhabha Atomic Research Centre, Mumbai (India). Fuel Chemistry Division

    2017-06-01

    Since plutonium possesses multiple oxidation states which can coexist in solution, a method for the identification of these oxidation states is important to understand its chemical processes. Liquid chromatographic studies were carried out to compare the chromatographic behaviour of different oxidation states of Pu in presence of the eluent, α-hydroxyisobutyric acid (HIBA). The three oxidation states of Pu viz. Pu(III), Pu(IV) and Pu(VI) were separated under optimised conditions. It was seen that the presence of the complexing agent influences the equilibrium of Pu(III)/(IV) as well as Pu(IV)/(VI) systems. Pu(III) to Pu(IV) conversion was found to be enhanced by high pH and concentration of HIBA whereas a relatively low pH and high concentration of HIBA promotes the conversion of Pu(VI) to Pu(IV).

  4. Reevaluation of JACS code system benchmark analyses of the heterogeneous system. Fuel rods in U+Pu nitric acid solution system

    Energy Technology Data Exchange (ETDEWEB)

    Takada, Tomoyuki; Miyoshi, Yoshinori; Katakura, Jun-ichi [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    2003-03-01

    In order to perform accuracy evaluation of the critical calculation by the combination of multi-group constant library MGCL and 3-dimensional Monte Carlo code KENO-IV among critical safety evaluation code system JACS, benchmark calculation was carried out from 1980 in 1982. Some cases where the neutron multiplication factor calculated in the heterogeneous system in it was less than 0.95 were seen. In this report, it re-calculated by considering the cause about the heterogeneous system of the U+Pu nitric acid solution systems containing the neutron poison shown in JAERI-M 9859. The present study has shown that the k{sub eff} value less than 0.95 given in JAERI-M 9859 is caused by the fact that the water reflector below a cylindrical container was not taken into consideration in the KENO-IV calculation model. By taking into the water reflector, the KENO-IV calculation gives a k{sub eff} value greater than 0.95 and a good agreement with the experiment. (author)

  5. Dissociation of diglycolamide complexes of Ln3+ (Ln = La-Lu) and An3+ (An = Pu, Am, Cm): redox chemistry of 4f and 5f elements in the gas phase parallels solution behavior.

    Science.gov (United States)

    Gong, Yu; Tian, Guoxin; Rao, Linfeng; Gibson, John K

    2014-11-17

    Tripositive lanthanide and actinide ions, Ln(3+) (Ln = La-Lu) and An(3+) (An = Pu, Am, Cm), were transferred from solution to gas by electrospray ionization as Ln(L)3(3+) and An(L)3(3+) complexes, where L = tetramethyl-3-oxa-glutaramide (TMOGA). The fragmentation chemistry of the complexes was examined by collision-induced and electron transfer dissociation (CID and ETD). Protonated TMOGA, HL(+), and Ln(L)(L-H)(2+) are the major products upon CID of La(L)3(3+), Ce(L)3(3+), and Pr(L)3(3+), while Ln(L)2(3+) is increasingly pronounced beyond Pr. A C-Oether bond cleavage product appears upon CID of all Ln(L)3(3+); only for Eu(L)3(3+) is the divalent complex, Eu(L)2(2+), dominant. The CID patterns of Pu(L)3(3+), Am(L)3(3+), and Cm(L)3(3+) are similar to those of the Ln(L)3(3+) for the late Ln. A striking exception is the appearance of Pu(IV) products upon CID of Pu(L)3(3+), in accord with the relatively low Pu(IV)/Pu(III) reduction potential in solution. Minor divalent Ln(L)2(2+) and An(L)2(2+) were produced for all Ln and An; with the exception of Eu(L)2(2+) these complexes form adducts with O2, presumably producing superoxides in which the trivalent oxidation state is recovered. ETD of Ln(L)3(3+) and An(L)3(3+) reveals behavior which parallels that of the Ln(3+) and An(3+) ions in solution. A C-Oether bond cleavage product, in which the trivalent oxidation state is preserved, appeared for all complexes; charge reduction products, Ln(L)2(2+) and Ln(L)3(2+), appear only for Sm, Eu, and Yb, which have stable divalent oxidation states. Both CID and ETD reveal chemistry that reflects the condensed-phase redox behavior of the 4f and 5f elements.

  6. The Virtual Employment Test Bed: An Immersive Synthetic Environment Allows Engineers to Test and Evaluate Material Solutions

    Science.gov (United States)

    2014-04-03

    synthetic environment allows engineers to test and evaluate material solutions Robert DeMarco, MSBME; Gordon Cooke, MEME ; John Riedener, MSSE...ROBERT DEMARCO, MSBME, is a Project Lead Engineer and Certified LabVIEW Associate Developer. GORDON COOKE, MEME , is a Principal Investigator at the

  7. Chain-length heterogeneity allows for the assembly of fatty acid vesicles in dilute solutions.

    Science.gov (United States)

    Budin, Itay; Prwyes, Noam; Zhang, Na; Szostak, Jack W

    2014-10-07

    A requirement for concentrated and chemically homogeneous pools of molecular building blocks would severely restrict plausible scenarios for the origin of life. In the case of membrane self-assembly, models of prebiotic lipid synthesis yield primarily short, single-chain amphiphiles that can form bilayer vesicles only at very high concentrations. These high critical aggregation concentrations (cacs) pose significant obstacles for the self-assembly of single-chain lipid membranes. Here, we examine membrane self-assembly in mixtures of fatty acids with varying chain lengths, an expected feature of any abiotic lipid synthesis. We derive theoretical predictions for the cac of mixtures by adapting thermodynamic models developed for the analogous phenomenon of mixed micelle self-assembly. We then use several complementary methods to characterize aggregation experimentally, and find cac values in close agreement with our theoretical predictions. These measurements establish that the cac of fatty acid mixtures is dramatically lowered by minor fractions of long-chain species, thereby providing a plausible route for protocell membrane assembly. Using an NMR-based approach to monitor aggregation of isotopically labeled samples, we demonstrate the incorporation of individual components into mixed vesicles. These experiments suggest that vesicles assembled in dilute, mixed solutions are depleted of the shorter-chain-length lipid species, a finding that carries implications for the composition of primitive cell membranes.

  8. Microscopic Calculations of 240Pu Fission

    Energy Technology Data Exchange (ETDEWEB)

    Younes, W; Gogny, D

    2007-09-11

    Hartree-Fock-Bogoliubov calculations have been performed with the Gogny finite-range effective interaction for {sup 240}Pu out to scission, using a new code developed at LLNL. A first set of calculations was performed with constrained quadrupole moment along the path of most probable fission, assuming axial symmetry but allowing for the spontaneous breaking of reflection symmetry of the nucleus. At a quadrupole moment of 345 b, the nucleus was found to spontaneously scission into two fragments. A second set of calculations, with all nuclear moments up to hexadecapole constrained, was performed to approach the scission configuration in a controlled manner. Calculated energies, moments, and representative plots of the total nuclear density are shown. The present calculations serve as a proof-of-principle, a blueprint, and starting-point solutions for a planned series of more comprehensive calculations to map out a large set of scission configurations, and the associated fission-fragment properties.

  9. Irradiation alternative method of manganese sulfate solution by a Pu-Be source for efficiency measurements; Metodo alternativo de irradiacao da solucao de sulfato de manganes por uma fonte de Pu-Be para medicoes de eficiencia

    Energy Technology Data Exchange (ETDEWEB)

    Silva, Fellipe Souza da; Martins, Marcelo Marques; Pereira, Walsan Wagner, E-mail: fellipess@ird.gov.br [Instituto de Radioprotecao e Dosimetria (IRD/CNEN-RJ), Rio de Janeiro, RJ (Brazil)

    2015-07-01

    This study intends to create an alternative irradiation system from a Plutonium-Beryllium source for manganese sulphate solution using the Monte Carlo code. Thus seeking to eliminate the issue of institutes that do not have reactors or particle accelerators in its infrastructure, in order to optimize and provide independence for them to carry out efficiency measurements of MnSO{sub 4} solution in their own locality. The Monte Carlo simulations defined the technical features of this new system so that the solution reaches the maximum neutron capture by manganese in solution. (author)

  10. Studies of the ternary systems humic substances - kaolinite - Pu(III) and Pu(IV)

    Energy Technology Data Exchange (ETDEWEB)

    Buda, R.A.; Kratz, J.V.; Trautmann, N. [Inst. fuer Kernchemie, Johannes-Gutenberg-Univ., Mainz (Germany); Banik, N.L. [Inst. fuer Kernchemie, Johannes-Gutenberg-Univ., Mainz (Germany); Inst. fuer Nukleare Entsorgung (INE), Forschungszentrum Karlsruhe (Germany)

    2008-07-01

    The behaviour of plutonium with respect to its migration in the aquifer has been studied under conditions close to nature. Most relevant under these conditions are Pu(III) and Pu(IV) in contact with humic substances (HS) and minerals. As a model for the host rock, kaolinite (KGa-1b) was chosen. The complexation of Pu(III) and Pu(IV) with Aldrich humic acid (AHA) in aqueous solution at ionic strength 0.1 M was investigated by the ultrafiltration method. The sorption of Pu(III) and Am(III) onto kaolinite (K) as a function of pH and metal-ion concentration was studied under aerobic and anaerobic conditions. The pH edge was found at pH {proportional_to} 5.5 independent of the metal-ion concentration and working atmosphere. The influence of HS on the sorption of Pu(III) and Pu(IV) onto kaolinite was investigated in the ternary systems Pu(III)-K-HS and Pu(IV)-K-HS and for comparison, in the system Th(IV)-K-HS. The dependence on pH, contact time, concentration of HS (for Pu(IV)-K-HS) was studied as well as the sequence in which the components were added. Generally, it was found that HS tend to enhance the sorption onto kaolinite below pH 6 and to decrease sorption at higher pH depending in detail on the sequence in which the components were added. An identification of the species sorbed on the surface of the kaolinite by X-ray absorption spectroscopy, as well as chemically, was attempted and preliminary results are discussed. (orig.)

  11. Synthesis of Pu-Doped Ceramic

    Energy Technology Data Exchange (ETDEWEB)

    Anderson, E. B

    1998-09-02

    Plutonium-doped zircon containing about 10 wt% Pu was synthesized in this cooperative project between Russia and the United States conducted at the V. G. Khlopin Radium Institute. The sol-gel method was used for starting precursor preparation to provide complete mixing of initial components and to avoid dust formation inside the glove-box. The sol-gel process also gives interim Pu stabilization in the form of amorphous zirconium hydrosilicate (AZHS), which is a result of gel solidification. AZHS is a solid and relatively durable material that can be easy converted into crystalline zircon by pressureless sintering, thus avoiding significant radioactive contamination of laboratory equipment. A methanol-aqueous solution of tetraethoxysilane Si(OC2H5)4, Pu-nitrate, and zirconil oxynitrate was prepared in final stoichiometry of zircon (Zr,Pu)SiO4 80 wt% + zirconia (Zr,Pu)O2 20 wt%. Gelation occurred after 90 hours at room temperature. AZHS with excess of zirconia 20 wt% was obtained as an interim calcine product and then it was converted into zircon/zirconia ceramic by sintering at 1490 to 1500°C in air for different time periods. The samples obtained were studied by SRD and ESEM methods. It was found that both zircon yield and zircon cell parameters that are correlated with Pu incorporation depend on sintering time.

  12. Anaerobic Biotransformation and Mobility of Pu and Pu-EDTA

    Energy Technology Data Exchange (ETDEWEB)

    Bolton, H., Jr.; Rai, D.; Xun, L.

    2005-04-18

    The complexation of radionuclides (e.g., plutonium (Pu) and {sup 60}Co) by codisposed ethylenediaminetetraacetate (EDTA) has enhanced their transport in sediments at DOE sites. Our previous NABIR research investigated the aerobic biodegradation and biogeochemistry of Pu(IV)-EDTA. Plutonium(IV) forms stable complexes with EDTA under aerobic conditions and an aerobic EDTA degrading bacterium can degrade EDTA in the presence of Pu and decrease Pu mobility. However, our recent studies indicate that while Pu(IV)-EDTA is stable in simple aqueous systems, it is not stable in the presence of relatively soluble Fe(III) compounds (i.e., Fe(OH){sub 3}(s)--2-line ferrihydrite). Since most DOE sites have Fe(III) containing sediments, Pu(IV) in likely not the mobile form of Pu-EDTA in groundwater. The only other Pu-EDTA complex stable in groundwater relevant to DOE sites would be Pu(III)-EDTA, which only forms under anaerobic conditions. Research is therefore needed in this brand new project to investigate the biotransformation of Pu and Pu-EDTA under anaerobic conditions. The biotransformation of Pu and Pu-EDTA under various anaerobic regimes is poorly understood including the reduction kinetics of Pu(IV) to Pu(III) from soluble (Pu(IV)-EDTA) and insoluble Pu(IV) as PuO2(am) by metal reducing bacteria, the redox conditions required for this reduction, the strength of the Pu(III)-EDTA complex, how the Pu(III)-EDTA complex competes with other dominant anoxic soluble metals (e.g., Fe(II)), and the oxidation kinetics of Pu(III)-EDTA. Finally, the formation of a stable soluble Pu(III)-EDTA complex under anaerobic conditions would require degradation of the EDTA complex to limit Pu(III) transport in geologic environments. Anaerobic EDTA degrading microorganisms have not been isolated. These knowledge gaps preclude the development of a mechanistic understanding of how anaerobic conditions will influence Pu and Pu-EDTA fate and transport to assess, model, and design approaches to stop

  13. The Application of Hydroxyurea in the Separation of U and Pu

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    The present paper suggests a novel salt-free organic agent to separate U and Pu in HNO3 solution. This agent is hydroxyurea(HU) which has strong reduction ability and also is a good chelating agent with a relatively simple structure. HU can rapidly reduce Pu(IV) to Pu(III) in HNO3 solution. The reduction can be to such extent that almost 100% Pu(IV) can be reduced to Pu(III) in 0.5 mol/L and 3.0 mol/L HNO3 solution. With the concentration less than 1.0 mol/L, HU has

  14. Pu-239 and Pu-240 inventories and Pu-240/ Pu-239 atom ratios in the water column off Sanriku, Japan.

    Science.gov (United States)

    Yamada, Masatoshi; Zheng, Jian; Aono, Tatsuo

    2013-04-01

    A magnitude 9.0 earthquake and subsequent tsunami occurred in the Pacific Ocean off northern Honshu, Japan, on 11 March 2011 which caused severe damage to the Fukushima Dai-ichi Nuclear Power Plant. This accident has resulted in a substantial release of radioactive materials to the atmosphere and ocean, and has caused extensive contamination of the environment. However, no information is available on the amounts of radionuclides such as Pu isotopes released into the ocean at this time. Investigating the background baseline concentration and atom ratio of Pu isotopes in seawater is important for assessment of the possible contamination in the marine environment. Pu-239 (half-life: 24,100 years), Pu-240 (half-life: 6,560 years) and Pu-241 (half-life: 14.325 years) mainly have been released into the environment as the result of atmospheric nuclear weapons testing. The atom ratio of Pu-240/Pu-239 is a powerful fingerprint to identify the sources of Pu in the ocean. The Pu-239 and Pu-240 inventories and Pu-240/Pu-239 atom ratios in seawater samples collected in the western North Pacific off Sanriku before the accident at Fukushima Dai-ichi Nuclear Power Plant will provide useful background baseline data for understanding the process controlling Pu transport and for distinguishing additional Pu sources. Seawater samples were collected with acoustically triggered quadruple PVC sampling bottles during the KH-98-3 cruise of the R/V Hakuho-Maru. The Pu-240/Pu-239 atom ratios were measured with a double-focusing SF-ICP-MS, which was equipped with a guard electrode to eliminate secondary discharge in the plasma and to enhance overall sensitivity. The Pu-239 and Pu-240 concentrations were 2.07 and 1.67 mBq/m3 in the surface water, respectively, and increased with depth; a subsurface maximum was identified at 750 m depth, and the concentrations decreased with depth, then increased at the bottom layer. The total Pu-239+240 inventory in the entire water column (depth interval 0

  15. DENSITY-FUNCTIONAL STUDY OF Zr-BASED ACTINIDE ALLOYS: 2. U-Pu-Zr SYSTEM

    Energy Technology Data Exchange (ETDEWEB)

    Landa, A; Soderlind, P; Turchi, P; Vitos, L; Ruban, A

    2009-02-09

    Density-functional theory, previously used to describe phase equilibria in the U-Zr alloys [1], is applied to study ground state properties of the bcc U-Pu-Zr solid solutions. Calculated heats of formation of the Pu-U and Pu-Zr alloys are in a good agreement with CALPHAD assessments. We found that account for spin-orbit coupling is important for successful description of Pu-containing alloys.

  16. Study on Analytical Method of Pu(Ⅲ, Ⅳ) and U(Ⅳ) in 1BP

    Institute of Scientific and Technical Information of China (English)

    LIU; Huan-liang; ZHANG; Li-hua; FAN; De-jun; WANG; Ling; QIAN; Hong-juan

    2013-01-01

    U(Ⅳ)is taken as reductant in uranium and plutonium separation process of China spent nuclear fuel reprocessing pilot plant.Rapid determining the concentrations of Pu(Ⅲ)/Pu(Ⅳ)and U(Ⅳ)in 1BP is vital to monitor 1B processing stage and condition the subsequent processing solution.A rapid method for determining the concentrations of Pu(Ⅲ)/Pu(Ⅳ)and U(Ⅳ)in 1BP was developed

  17. LA-ICP-MS for Pu source identification at Mayak PA, the Urals, Russia.

    Science.gov (United States)

    Cagno, S; Hellemans, K; Lind, O C; Skipperud, L; Janssens, K; Salbu, B

    2014-02-01

    Information on Pu in environmental samples is traditionally based on the determination of the (240+239)Pu activity via Alpha Spectrometry (AS). A large number of alpha spectrometry sources (planchettes) containing radiochemically separated Pu are therefore stored worldwide and are available for further analyses. These archive samples represent a resource from which valuable information on isotopic composition of alpha emitters including Pu can be obtained. The relative abundances of Pu isotopes can be used to trace specific Pu sources and characterize the relative contributions of different Pu sources in a sample. Thus, in addition to the total (239+240)Pu activity, determination of the (240)Pu/(239)Pu ratio can provide valuable information on the nature of the Pu emitting sources. The Pu isotopic ratios can be determined by mass spectrometry techniques such as Sector Field Inductively Coupled Plasma Mass Spectrometry (SF-ICPMS) or Accelerator Mass Spectrometry (AMS) that require dissolution and complete destruction of the material deposited on the planchettes. In this study Laser Ablation (LA)-quadrupole-ICP-MS has been employed for the analysis of (239)Pu/(240)Pu ratios from alpha-planchettes prepared from samples originating from the Mayak PA nuclear facility, Russia. The results are compared with data from AMS and show that the (240)Pu/(239)Pu ratios obtained by LA-ICP-MS can be utilized to distinguish weapons-grade Pu from civil reprocessing sources. Moreover, isotope ratio mapping can also be performed across the planchettes, allowing e.g. the visualization of possible inhomogeneities in the Pu-isotope distribution on their surface. Thus, this solid sample technique can be applied to extract additional information from existing archives of samples.

  18. Hydrolysis of trivalent plutonium and solubility of Pu(OH)3 (am) under electrolytic reducing conditions.

    Science.gov (United States)

    Cho, Hye-Ryun; Youn, Young-Sang; Jung, Euo Chang; Cha, Wansik

    2016-12-06

    The aim of this work is to determine the solubility product of plutonium hydroxide under reducing conditions and to ascertain the stability of Pu(OH)3 (am) in water. Hydrolysis of Pu(iii) and solubility of Pu(OH)3 (am) were investigated at a constant ionic strength of 0.1 M NaClO4. Coulometric titration was adopted to adjust the pH of plutonium solutions, during which the electrolytic reducing conditions maintained the oxidation state of Pu(iii). Chemical speciation for dissolved plutonium was investigated using sensitive spectrophotometry coupled with a liquid waveguide capillary cell. The spectroscopic investigations indicated that dissolved Pu(iv), Pu(v), and Pu(vi) species were ignorable under these experimental conditions. The absorbance of Pu(3+) ions decreased due to hydrolysis of Pu(iii) but the absorbance of Pu(iii) hydrolysis species was not distinguishable. The formation constant for the first hydrolysis species (log (*)β'1) determined in the present study is -6.62 ± 0.25. The non-crystalline structure of the plutonium precipitate was observed through X-ray diffraction. The solubility product of Pu(OH)3 (am), log (*)K's,0 is determined to be 15.23 ± 0.50. These results indicate a stronger tendency for the hydrolysis of Pu(iii) and higher stability (lower solubility) of Pu(OH)3 (am) compared to Am(iii).

  19. Reductive dissolution of Pu(IV) by Clostridium sp. under anaerobic conditions.

    Science.gov (United States)

    Francis, Arokiasamy J; Dodge, Cleveland J; Gillow, Jeffrey B

    2008-04-01

    An anaerobic, gram positive, spore-forming bacterium Clostridium sp., common in soils and wastes, capable of reduction of Fe(III) to Fe(II), Mn(IV) to Mn(II), Tc(VII) to Tc(IV), and U(VI) to U(IV), reduced Pu(IV) to Pu(III). Addition of 242Pu (IV)-nitrate to the bacterial growth medium at pH 6.4 resulted in the precipitation of Pu as amorphous Pu(OH)4 due to hydrolysis and polymerization reactions. The Pu (1 x 10(-5) M) had no effect upon growth of the bacterium as evidenced by glucose consumption; carbon dioxide and hydrogen production; a decrease in pH of the medium from 6.4 to 3.0 due to production of acetic and butyric acids from glucose fermentation; and a change in the Eh of the culture medium from +50 to -180 mV. Commensurate with bacterial growth, Pu was rapidly solubilized as evidenced by an increase in Pu concentration in solution which passed through a 0.03 microm filtration. Selective solvent extraction of the culture by thenoyltrifluoroacetone (TTA) indicated the presence of a reduced Pu species in the soluble fraction. X-ray absorption near edge spectroscopic (XANES) analysis of Pu in the culture sample at the Pu LIII absorption edge (18.054 keV) showed a shift of -3 eV compared to a Pu(IV) standard indicating reduction of Pu(IV) to Pu(III). These results suggestthat, although Pu generally exists as insoluble Pu(IV) in the environment, under appropriate conditions, anaerobic microbial activity could affect the long-term stability and mobility of Pu by its reductive dissolution.

  20. Synthesis, characterization, kinetic and thermodynamic studies of the dissolution of ThO{sub 2} and of solid solutions Th{sub 1-x}M{sub x}O{sub 2} (M = U, Pu); Synthese, caracterisation et etudes cinetique et thermodynamique de la dissolution de ThO{sub 2} et des solutions solides Th{sub 1-x}M{sub x}O{sub 2} (M = U, Pu)

    Energy Technology Data Exchange (ETDEWEB)

    Heisbourg, G

    2003-12-01

    The aim of this work was to understand the mechanisms of dissolution of ThO{sub 2} and of thorium mixed oxides such as Th{sub 1-x}U{sub x}O{sub 2} and Th{sub 1-x}Pu{sub x}O{sub 2} in aqueous, oxygenated or inert media. Several solids have been synthesized by precipitation in oxalic medium: Th{sub 1-x}U{sub x}O{sub 2} (x= 0.11; 0.24; 0.37; 0.53; 0.67; 0.81 and 0.91) and Th{sub 1-x}Pu{sub x}O{sub 2} (x= 0.13; 0.32 and 0.66). They have been characterized by XRD, SEM, TEM, XPS, XAS, PIXE and EPMA. The sintering conditions of these materials have been studied and optimized in order to obtain sintered samples with a measured density very near the theoretical densities. A kinetic study of the dissolution of ThO{sub 2} and of solid solutions Th{sub 1-x}U{sub x}O{sub 2} has been carried out in several aqueous media (HNO{sub 3}, HCl, H{sub 2}SO{sub 4}) in terms of several parameters: protons concentration, temperature, pH, ionic strength, nature of the electrolyte solution and uranium molar ratio for the solid solutions Th{sub 1-x}U{sub x}O{sub 2} in order to determine the kinetic laws of dissolution of the solid solutions having different compositions comparatively to ThO{sub 2}. The leaching tests carried out in natural waters of compositions near those of the deep geologic sites considered for the storage of nuclear wastes have shown that the dissolution of the solids was bound to the complexing effect of the constitutional ions of the water considered. The leaching tests carried out on sintered samples of the same composition have led to the same normalized dissolution velocities. The thermodynamic aspect of the dissolution of the solid solutions Th{sub 1-x}U{sub x}O{sub 2} in nitric medium has been studied at last. (O.M.)

  1. AFS-2 FLOWSHEET MODIFICATIONS TO ADDRESS THE INGROWTH OF PU(VI) DURING METAL DISSOLUTION

    Energy Technology Data Exchange (ETDEWEB)

    Crapse, K.; Rudisill, T.; O' Rourke, P.; Kyser, E.

    2014-07-02

    In support of the Alternate Feed Stock Two (AFS-2) PuO{sub 2} production campaign, Savannah River National Laboratory (SRNL) conducted a series of experiments concluding that dissolving Pu metal at 95°C using a 6–10 M HNO{sub 3} solution containing 0.05–0.2 M KF and 0–2 g/L B could reduce the oxidation of Pu(IV) to Pu(VI) as compared to dissolving Pu metal under the same conditions but at or near the boiling temperature. This flowsheet was demonstrated by conducting Pu metal dissolutions at 95°C to ensure that PuO{sub 2} solids were not formed during the dissolution. These dissolution parameters can be used for dissolving both Aqueous Polishing (AP) and MOX Process (MP) specification materials. Preceding the studies reported herein, two batches of Pu metal were dissolved in the H-Canyon 6.1D dissolver to prepare feed solution for the AFS-2 PuO{sub 2} production campaign. While in storage, UV-visible spectra obtained from an at-line spectrophotometer indicated the presence of Pu(VI). Analysis of the solutions also showed the presence of Fe, Ni, and Cr. Oxidation of Pu(IV) produced during metal dissolution to Pu(VI) is a concern for anion exchange purification. Anion exchange requires Pu in the +4 oxidation state for formation of the anionic plutonium(IV) hexanitrato complex which absorbs onto the resin. The presence of Pu(VI) in the anion feed solution would require a valence adjustment step to prevent losses. In addition, the presence of Cr(VI) would result in absorption of chromate ion onto the resin and could limit the purification of Pu from Cr which may challenge the purity specification of the final PuO{sub 2} product. Initial experiments were performed to quantify the rate of oxidation of Pu(IV) to Pu(VI) (presumed to be facilitated by Cr(VI)) as functions of the HNO{sub 3} concentration and temperature in simulated dissolution solutions containing Cr, Fe, and Ni. In these simulated Pu dissolutions studies, lowering the temperature from near boiling

  2. Surface-mediated formation of Pu(IV) nanoparticles at the muscovite-electrolyte interface.

    Science.gov (United States)

    Schmidt, Moritz; Lee, Sang Soo; Wilson, Richard E; Knope, Karah E; Bellucci, Francesco; Eng, Peter J; Stubbs, Joanne E; Soderholm, L; Fenter, P

    2013-12-17

    The formation of Pu(IV)-oxo-nanoparticles from Pu(III) solutions by a surface-enhanced redox/polymerization reaction at the muscovite (001) basal plane is reported, with a continuous increase in plutonium coverage observed in situ over several hours. The sorbed Pu extends >70 Å from the surface with a maximum concentration at 10.5 Å and a total coverage of >9 Pu atoms per unit cell area of muscovite (0.77 μg Pu/cm(2)) (determined independently by in situ resonant anomalous X-ray reflectivity and by ex-situ alpha-spectrometry). The presence of discrete nanoparticles is confirmed by high resolution atomic force microscopy. We propose that the formation of these Pu(IV) nanoparticles from an otherwise stable Pu(III) solution can be explained by the combination of a highly concentrated interfacial Pu-ion species, the Pu(III)-Pu(IV) redox equilibrium, and the strong proclivity of tetravalent Pu to hydrolyze and form polymeric species. These results are the first direct observation of such behavior of plutonium on a naturally occurring mineral, providing insights into understanding the environmental transport of plutonium and other contaminants capable of similar redox/polymerization reactions.

  3. Biodegradation of PuEDTA and Impacts on Pu Mobility

    Energy Technology Data Exchange (ETDEWEB)

    Bolton, H., Jr.; Rai, D.; Xun, L.

    2004-03-17

    The contamination of many DOE sites by Pu presents a long-term problem because of its long half-life (240,000 yrs) and the low drinking water standard (<10{sup -12} M). EDTA was co-disposed with radionuclides (e.g., Pu, {sup 60}Co), formed strong complexes, and enhanced radionuclide transport at several DOE sites. Biodegradation of EDTA should decrease Pu mobility. One objective of this project was to determine the biodegradation of EDTA in the presence of PuEDTA complexes. The aqueous system investigated at pH 7 (10{sup -4} M EDTA and 10{sup -6} M Pu) contained predominantly Pu(OH){sub 2}EDTA{sup 2-}. The EDTA was degraded at a faster rate in the presence of Pu. As the total concentration of both EDTA and PuEDTA decreased (i.e., 10{sup -5} M EDTA and 10{sup -7} M PuEDTA), the presence of Pu decreased the biodegradation rate of the EDTA. It is currently unclear why the concentration of Pu directly affects the increase/decrease in rate of EDTA biodegradation. The soluble Pu concentration decreased, in agreement with thermodynamic predictions, as the EDTA was biodegraded, indicating that biodegradation of EDTA will decrease Pu mobility when the Pu is initially present as Pu(IV)EDTA. A second objective was to investigate how the presence of competing metals, commonly encountered in geologic media, will influence the speciation and biodegradation of Pu(IV)-EDTA. Studies on the solubilities of Fe(OH){sub 3}(s) and of Fe(OH){sub 3}(s) plus PuO{sub 2}(am) in the presence of EDTA and as a function of pH showed that Fe(III) out competes the Pu(IV) for the EDTA complex, thereby showing that Pu(IV) will not form stable complexes with EDTA for enhanced transport of Pu in Fe(III) dominated subsurface systems. A third objective is to investigate the genes and enzymes involved in EDTA biodegradation. BNC1 can use EDTA and another synthetic chelating agent nitrilotriacetate (NTA) as sole carbon and nitrogen sources. The same catabolic enzymes are responsible for both EDTA and NTA

  4. Angular distributions of low-spin states in {sup 240}Pu by means of the {sup 242}Pu(p,t){sup 240}Pu reaction

    Energy Technology Data Exchange (ETDEWEB)

    Spieker, Mark; Endres, Janis; Pascu, Sorin; Zilges, Andreas [Koeln Univ. (Germany). Inst. fuer Kernphysik; Bucurescu, Dorel; Zamfir, Nicolae-Victor [Horia Hulubei National Institute of Physics and Nuclear Engineering, Bucharest (Romania); Faestermann, Thomas [Physik Department, Technische Universitaet Muenchen (Germany); Hertenberger, Ralf; Wirth, Hans-Friedrich [Fakultaet fuer Physik, Ludwig-Maximilians-Universitaet Muenchen (Germany)

    2013-07-01

    Since recent experimental and theoretical studies revealed the importance of octupole correlations in the actinide region and especially in {sup 240}Pu, a {sup 242}Pu(p,t){sup 240}Pu experiment has been conducted at the Q3D magnetic spectrograph of the Maier-Leibnitz laboratory in Munich. Excited states in {sup 240}Pu were investigated up to an excitation energy of 3 MeV. Angular distributions have been measured at 9 laboratory angles between 5 {sup circle} and 40 {sup circle}. The comparison of the experimental angular distributions with DWBA calculations allowed the assignment of several low-spin states. Most of them were seen for the first time. The experimental data, especially the data on the 21 J{sup π}= 0{sup +} states, are presented and discussed in the framework of the spdf-version of the Interacting Boson Model.

  5. Elastic properties of Pu metal and Pu-Ga alloys

    Energy Technology Data Exchange (ETDEWEB)

    Soderlind, P; Landa, A; Klepeis, J E; Suzuki, Y; Migliori, A

    2010-01-05

    We present elastic properties, theoretical and experimental, of Pu metal and Pu-Ga ({delta}) alloys together with ab initio equilibrium equation-of-state for these systems. For the theoretical treatment we employ density-functional theory in conjunction with spin-orbit coupling and orbital polarization for the metal and coherent-potential approximation for the alloys. Pu and Pu-Ga alloys are also investigated experimentally using resonant ultrasound spectroscopy. We show that orbital correlations become more important proceeding from {alpha} {yields} {beta} {yields} {gamma} plutonium, thus suggesting increasing f-electron correlation (localization). For the {delta}-Pu-Ga alloys we find a softening with larger Ga content, i.e., atomic volume, bulk modulus, and elastic constants, suggest a weakened chemical bonding with addition of Ga. Our measurements confirm qualitatively the theory but uncertainties remain when comparing the model with experiments.

  6. Elastic properties of Pu metal and Pu-Ga alloys

    Science.gov (United States)

    Söderlind, Per; Landa, Alex; Klepeis, J. E.; Suzuki, Y.; Migliori, A.

    2010-06-01

    We present elastic properties, theoretical and experimental, of Pu metal and Pu-Ga (δ) alloys together with ab initio equilibrium equation of state for these systems. For the theoretical treatment we employ density-functional theory in conjunction with spin-orbit coupling and orbital polarization for the metal and coherent-potential approximation for the alloys. Pu and Pu-Ga alloys are also investigated experimentally using resonant ultrasound spectroscopy. We show that orbital correlations become more important proceeding from α→β→γ plutonium, thus suggesting increasing f -electron correlation and a corresponding softening of the elastic moduli. For the δ-Pu-Ga alloys we find a softening with larger Ga content, i.e., atomic volume, bulk modulus, and elastic constants imply a weakened chemical bonding with addition of Ga. Our measurements confirm qualitatively the theory but uncertainties remain when comparing the model with experiments.

  7. Pu oxidation state distributions in suspensions of the Mont Terri Opalinus Clay isolate Sporomusa sp. MT-2.99

    Energy Technology Data Exchange (ETDEWEB)

    Moll, Henry [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Biogeochemistry; Cherkouk, Andrea [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). HZDR Young Investigator Group; Bok, Frank [Helmholtz-Zentrum Dresden-Rossendorf e.V., Dresden (Germany). Surface Processes

    2017-06-01

    The time-dependent {sup 242}Pu oxidation state distribution in the presence of Sporomusa sp. cells as a function of pH with or without Na-pyruvate was analyzed. In all cases, the presence of bacterial cells enhanced removal of Pu from solution and accelerated Pu interaction reactions, e.g. biosorption and bioreduction.

  8. REACT-Mod: a mathematical model for transient calculation of chemical reactions with U-Pu-Np-Tc in the aqueous nitric acid solution

    Energy Technology Data Exchange (ETDEWEB)

    Tachimori, Shoichi [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment; Kitamura, Tatsuaki

    1996-10-01

    A computer code REACT-Mod which simulates various chemical reactions in an aqueous nitric acid solution involving uranium, plutonium, neptunium, technetium etc. e.g., redox, radiolytic and disproportionation reactions of 68, was developed based on the kinetics model. The numerical solution method adopted in the code are two, a kinetics model totally based on the rate law of which differential equations are solved by the modified Porsing method, and a two-step model based on both the rate law and equilibrium law. Only the former treats 27 radiolytic reactions. The latter is beneficially used to have a quick and approximate result by economical computation. The present report aims not only to explain the concept, chemical reactions treated and characteristics of the model but also to provide details of the program for users of the REACT-Mod code. (author)

  9. Reactions of plutonium with aceto-hydroxamic acid in aqueous solutions: first results

    Energy Technology Data Exchange (ETDEWEB)

    Butler, R.J.; Renshaw, J.C.; Collison, D.; Livens, F.R. [Manchester Univ. (United Kingdom). Dept. of Chemistry; Sinkov, S.; Choppin, G.R. [Florida State Univ., Tallahassee, FL (United States). Dept. of Chemistry; Taylor, R.J. [BNFL, Research and Technology, Sellafield, Seascale, Cumbria (United Kingdom)

    2000-07-01

    Optical spectroscopy has been used to follow the complexation reactions of Pu(IV) and Pu(VI) with the acetohydroxamate (AHA{sup -}) ligand. Significant reduction of Pu(IV) to Pu(III) occurs in the course of the experiment, although the experimental procedure has now been modified to suppress this and will allow Pu(IV)-AHA stability constants to be calculated. In the case of the Pu(VI)-AHA reaction, significant reduction occurs immediately, forming successively Pu(V), Pu(IV) and eventually Pu(III). This reaction was followed for 6 days, by which time Pu(VI) was quantitatively reduced to Pu(III). (authors)

  10. Genome-scale definition of the transcriptional programme associated with compromised PU.1 activity in acute myeloid leukaemia.

    Science.gov (United States)

    Sive, J I; Basilico, S; Hannah, R; Kinston, S J; Calero-Nieto, F J; Göttgens, B

    2016-01-01

    Transcriptional dysregulation is associated with haematological malignancy. Although mutations of the key haematopoietic transcription factor PU.1 are rare in human acute myeloid leukaemia (AML), they are common in murine models of radiation-induced AML, and PU.1 downregulation and/or dysfunction has been described in human AML patients carrying the fusion oncogenes RUNX1-ETO and PML-RARA. To study the transcriptional programmes associated with compromised PU.1 activity, we adapted a Pu.1-mutated murine AML cell line with an inducible wild-type PU.1. PU.1 induction caused transition from leukaemia phenotype to monocytic differentiation. Global binding maps for PU.1, CEBPA and the histone mark H3K27Ac with and without PU.1 induction showed that mutant PU.1 retains DNA-binding ability, but the induction of wild-type protein dramatically increases both the number and the height of PU.1-binding peaks. Correlating chromatin immunoprecipitation (ChIP) Seq with gene expression data, we found that PU.1 recruitment coupled with increased histone acetylation induces gene expression and activates a monocyte/macrophage transcriptional programme. PU.1 induction also caused the reorganisation of a subgroup of CEBPA binding peaks. Finally, we show that the PU.1 target gene set defined in our model allows the stratification of primary human AML samples, shedding light on both known and novel AML subtypes that may be driven by PU.1 dysfunction.

  11. Thermodynamic assessment of the Th–U–Pu system

    Energy Technology Data Exchange (ETDEWEB)

    Beneš, O., E-mail: ondrej.benes@ec.europa.eu; Manara, D.; Konings, R.J.M.

    2014-06-01

    Thermodynamic assessments of the Th–U and Th–Pu binary systems are performed in this study according to CALPHAD method and together with the data on the U–Pu system, which has been already published in the literature, the Th–U–Pu ternary system is determined. All available experimental data from the literature were used for the binary system assessments and based on them the Gibbs energy properties of the unknown phases have been optimized. For the excess Gibbs energy of the liquid phase the ionic liquid model has been used, whereas for solid solutions the Redlich–Kister description was selected. In case of the Th–U and Th–Pu binary systems a very good agreement between the assessment and the experimental equilibrium data has been achieved, with 80% of equilibrium data reproduced within ±20 K.

  12. Plutonium isotopes 238Pu, 239+240Pu, 241Pu and 240Pu/239Pu atomic ratios in the southern Baltic Sea ecosystem

    Directory of Open Access Journals (Sweden)

    Dagmara I. Strumińska-Parulska

    2010-09-01

    Full Text Available The paper summarizes the results of plutonium findings in atmospheric fallout samples and marine samples from the southern Baltic Sea during our research in 1986-2007. The activities of 238Pu and 239+240Pu isotopes were measured with an alpha spectrometer. The activities of 241Pu were calculated indirectly by 241Am activity measurements 16-18 years after the Chernobyl accident. The 240Pu/239Pu atomic ratios were measured using accelerator mass spectrometry (AMS. The 241Pu activities indicate that the main impact of the Chernobyl accident was on the plutonium concentration in the components of the Baltic Sea ecosystem examined in this work. The highest 241Pu/239+240Pu activity ratio was found in sea water (140 ± 33. The AMS measurements of atmospheric fallout samples collected during 1986 showed a significant increase in the 240Pu/239Pu atomic ratio from 0.29 ± 0.04 in March 1986 to 0.47 ± 0.02 in April 1986.

  13. Ultra-trace determination of (90)Sr, (137)Cs, (238)Pu, (239)Pu, and (240)Pu by triple quadruple collision/reaction cell-ICP-MS/MS: Establishing a baseline for global fallout in Qatar soil and sediments.

    Science.gov (United States)

    Amr, Mohamed A; Helal, Abdul-Fattah I; Al-Kinani, Athab T; Balakrishnan, Perumal

    2016-03-01

    The development of practical, fast, and reliable methods for the ultra-trace determination of anthropogenic radionuclides (90)Sr, (137)Cs, (238)Pu, (239)Pu, and (240)Pu by triple quadruple collision/reaction cell inductively coupled plasma mass spectrometry (CRC-ICP-MS/MS) were investigated in term of its accuracy and precision for producing reliable results. The radionuclides were extracted from 1 kg of the environmental soil samples by concentrated nitric and hydrochloric acids. The leachate solutions were measured directly by triple quadrupole CRC-ICP-MS/MS. For quality assurance, a chemical separation of the concerned radionuclides was conducted and then measured by single quadrupole-ICP-MS. The developed methods were next applied to measure the anthropogenic radionuclides (90)Sr, (137)Cs, (238)Pu, (239)Pu, and (240)Pu in soil samples collected throughout the State of Qatar. The average concentrations of (90)Sr, (137)Cs, (238)Pu, (239)Pu, and (240)Pu were 0.606 fg/g (3.364 Bq/kg), 0.619 fg/g (2.038 Bq/kg), 0.034 fg/g (0.0195 Bq/kg), 65.59 fg/g (0.150 Bq/kg), and 12.06 fg/g (0.103 Bq/kg), respectively.

  14. Heterogeneous reduction of PuO₂ with Fe(II): importance of the Fe(III) reaction product.

    Science.gov (United States)

    Felmy, Andrew R; Moore, Dean A; Rosso, Kevin M; Qafoku, Odeta; Rai, Dhanpat; Buck, Edgar C; Ilton, Eugene S

    2011-05-01

    Heterogeneous reduction of actinides in higher, more soluble oxidation states to lower, more insoluble oxidation states by reductants such as Fe(II) has been the subject of intensive study for more than two decades. However, Fe(II)-induced reduction of sparingly soluble Pu(IV) to the more soluble lower oxidation state Pu(III) has been much less studied, even though such reactions can potentially increase the mobility of Pu in the subsurface. Thermodynamic calculations are presented that show how differences in the free energy of various possible solid-phase Fe(III) reaction products can greatly influence aqueous Pu(III) concentrations resulting from reduction of PuO₂(am) by Fe(II). We present the first experimental evidence that reduction of PuO₂(am) to Pu(III) by Fe(II) was enhanced when the Fe(III) mineral goethite was spiked into the reaction. The effect of goethite on reduction of Pu(IV) was demonstrated by measuring the time dependence of total aqueous Pu concentration, its oxidation state, and system pe/pH. We also re-evaluated established protocols for determining Pu(III) {[Pu(III) + Pu(IV)] - Pu(IV)} by using thenoyltrifluoroacetone (TTA) in toluene extractions; the study showed that it is important to eliminate dissolved oxygen from the TTA solutions for accurate determinations. More broadly, this study highlights the importance of the Fe(III) reaction product in actinide reduction rate and extent by Fe(II).

  15. Adsorption of Pu(IV) Polymer onto 304L Stainless Steel

    Energy Technology Data Exchange (ETDEWEB)

    Bronikowski, M.G.

    1999-07-16

    'The report, Technical Basis for Safe Operations with Pu-239 Polymer in NMS&S Operating Facilities (F & H Areas), (WSRC-TR-99-00008) was issued in an effort to upgrade the Authorization Basis (AB) for H Area facilities relative to nuclear criticality. At the time, insufficient data were found in the literature to quantify the adsorption of Pu polymer onto the surfaces of stainless steel tanks. Additional experimental or literature information on the adsorption of Pu(IV) polymer and its removal was deemed necessary to support the H Area AB. The results obtained are also applicable to processing in F Area facilities.Additional literature sources suggest that adsorption on the tank walls should not be a safety concern. The sources show that the amount of Pu polymer that adsorbs from a solution comes to a limiting amount in 5 to 7 days after which no additional Pu is adsorbed. Adsorption increases with Pu concentration and decreases with acid concentration. The adsorbed amounts are small varying from 0.5 mg/cm2 for a 0.5 g/l Pu / 0.5M HNO3 solution to 11 mg/cm2 for a 1-3 g/l Pu / 0.1M HNO3 solution. Additionally, acid concentrations greater than 0.1M will remove a percentage of adsorbed Pu.The experimental results have generally confirmed much of what has been reported in the literature. Specifically, adsorption onto stainless steel was found to increase with increased Pu concentration, and decreased acid concentration. The amount adsorbed was found to come to a limiting amount after 5 to 7 days. Pu adsorbed as polymer was found to be harder to remove than if it was adsorbed as Pu(IV). The amount of Pu adsorbed as polymer was found to be almost an order of magnitude more than that from a similar concentration Pu(IV) solution. Unlike the literature, only a slight increase in adsorption values was found when the steel surface was removed, dried, and replaced in the Pu solution. The amount of Pu as polymer which would adsorb onto the surface of a 14,000L tank was

  16. Radiative capture on $^{242}$Pu for MOX fuel reactors

    CERN Multimedia

    The use of MOX fuel (mixed-oxide fuel made of UO$_{2}$ and PuO$_{2}$) in nuclear reactors allows substituting a large fraction of the enriched Uranium by Plutonium reprocessed from spent fuel. Indeed around 66% of the plutonium from spent fuel is made of $^{239}$Pu and $^{241}$Pu, which are fissile in thermal reactors. A typical reactor of this type uses a fuel with 7% reprocessed Pu and 93% depleted U, thus profiting from both the spent fuel and the remaining $^{238}$U following the $^{235}$U enrichment. With the use of such new fuel compositions rich in Pu the better knowledge of the capture and fission cross sections of the Pu isotopes becomes very important. This is clearly stated in the recent OECD NEA’s “High Priority Request List” and in the WPEC-26 “Uncertainty and target accuracy assessment for innovative systems using recent covariance data evaluations” report. In particular, a new series of cross section evaluations have been recently carried out jointly by the European (JEFF) and United ...

  17. PU-ICE Summary Information.

    Energy Technology Data Exchange (ETDEWEB)

    Moore, Michael [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

    2017-05-01

    The Generator Knowledge Report for the Plutonium Isentropic Compression Experiment Containment Systems (GK Report) provides information for the Plutonium Isentropic Compression Experiment (Pu- ICE) program to support waste management and characterization efforts. Attachment 3-18 presents generator knowledge (GK) information specific to the eighteenth Pu-ICE conducted in August 2015, also known as ‘Shot 18 (Aug 2015) and Pu-ICE Z-2841 (1).’ Shot 18 (Aug 2015) was generated on August 28, 2015 (1). Calculations based on the isotopic content of Shot 18 (Aug 2015) and the measured mass of the containment system demonstrate the post-shot containment system is low-level waste (LLW). Therefore, this containment system will be managed at Sandia National Laboratory/New Mexico (SNL/NM) as LLW. Attachment 3-18 provides documentation of the TRU concentration and documents the concentration of any hazardous constituents.

  18. Decreased solubilization of Pu(IV) polymers by humic acids under anoxic conditions

    Science.gov (United States)

    Xie, Jinchuan; Lin, Jianfeng; Liang, Wei; Li, Mei; Zhou, Xiaohua

    2016-11-01

    Pu(IV) polymer has a very low solubility (log[Pu(IV)aq]total = -10.4 at pH 7.2 and I = 0). However, some aspects of their environmental fate remain unclear. Humic acids are able to complex with Pu4+ ions and their dissolved species (EDTA ligands. In contrast, the dissolved humic acids did not solubilize the polymers but in fact decreased their solubility by one order of magnitude. The humic coatings were responsible for the decreased solubilization. Such coatings limited the contact between the polymers and EDTA ligands, especially at the relatively high concentrations of humic acids (>0.57 mg/L). Solubilization of the humic-coated polymers was thus inhibited to a significant extent although EDTA, having the great complexation ability, was present in the humic solutions. Reduction of Pu(IV) polymers by the humic acids was also not observed in the absence of EDTA. In the presence of EDTA, the polymers were partially reduced to Pu(III)aq by the humic acids of 0.57 mg/L and the percentage of Pu(III)aq accounted for 51.7% of the total aqueous Pu. This demonstrates that the humic acids were able to reduce the aqueous Pu(IV), instead of the polymeric Pu(IV). Such a demonstration is supported by the very positive redox potential of aqueous Pu(IV)-EDTA complex: Eho ‧ (PuL24-/PuL25-) = 154.3 mV >>Eh (PuO2 (am) /Pu3+) = -182.7 mV calculated at 10-10 mol/L Pu3+ and pH 7.2. At the higher humic concentrations (>0.57 mg/L), the polymers were reduced to a lesser extent because the much denser humic coatings resulted in lower concentrations of the aqueous Pu(IV). Consequently, humic acids make Pu(IV) polymers pretty stable unless the artificial ligands such as EDTA are present in the groundwater.

  19. Electrochemical behavior of U and Pu in the molten salts

    Energy Technology Data Exchange (ETDEWEB)

    Shirai, Osamu; Iwai, Takashi; Arai, Yasuo [Japan Atomic Energy Research Inst., Oarai, Ibaraki (Japan). Oarai Research Establishment; Uozumi, Kohichi [Central Research Inst. of Electric Power Industry, Tokyo (Japan)

    2001-12-01

    Thermodynamic evaluation are performed for the diffusion coefficient and oxidation redaction potential of U and Pu in the LiCl-KCl eutectic salt through the measurements of their electrodeposition and solution by electric cyclic-voltammetry and potentiometry. On the electrode reaction of U and Pu at the liquid electrode (Cd, Bi) the positive-shift reaction mechanism of oxidation reduction potential is made clear, which is important in the development of dry reprocessing technology. The formation free energy of the metallic compound with Cd or Bi is also evaluated. (H. Katsuta)

  20. Determination of plutonium isotopes (238Pu, 239Pu, 240Pu, 241Pu) in environmental samples using radiochemical separation combined with radiometric and mass spectrometric measurements.

    Science.gov (United States)

    Xu, Yihong; Qiao, Jixin; Hou, Xiaolin; Pan, Shaoming; Roos, Per

    2014-02-01

    This paper reports an analytical method for the determination of plutonium isotopes ((238)Pu, (239)Pu, (240)Pu, (241)Pu) in environmental samples using anion exchange chromatography in combination with extraction chromatography for chemical separation of Pu. Both radiometric methods (liquid scintillation counting and alpha spectrometry) and inductively coupled plasma mass spectrometry (ICP-MS) were applied for the measurement of plutonium isotopes. The decontamination factors for uranium were significantly improved up to 7.5 × 10(5) for 20 g soil compared to the level reported in the literature, this is critical for the measurement of plutonium isotopes using mass spectrometric technique. Although the chemical yield of Pu in the entire procedure is about 55%, the analytical results of IAEA soil 6 and IAEA-367 in this work are in a good agreement with the values reported in the literature or reference values, revealing that the developed method for plutonium determination in environmental samples is reliable. The measurement results of (239+240)Pu by alpha spectrometry agreed very well with the sum of (239)Pu and (240)Pu measured by ICP-MS. ICP-MS can not only measure (239)Pu and (240)Pu separately but also (241)Pu. However, it is impossible to measure (238)Pu using ICP-MS in environmental samples even a decontamination factor as high as 10(6) for uranium was obtained by chemical separation.

  1. CHILD ALLOWANCE

    CERN Multimedia

    Human Resources Division

    2001-01-01

    HR Division wishes to clarify to members of the personnel that the allowance for a dependent child continues to be paid during all training courses ('stages'), apprenticeships, 'contrats de qualification', sandwich courses or other courses of similar nature. Any payment received for these training courses, including apprenticeships, is however deducted from the amount reimbursable as school fees. HR Division would also like to draw the attention of members of the personnel to the fact that any contract of employment will lead to the suppression of the child allowance and of the right to reimbursement of school fees.

  2. Combined effects of Fe(II) and oxidizing radiolysis products on UO2 and PuO2 dissolution in a system containing solid UO2 and PuO2

    Science.gov (United States)

    Amme, Marcus; Pehrman, Reijo; Deutsch, Rudolf; Roth, Olivia; Jonsson, Mats

    2012-11-01

    The stability of UO2 spent nuclear fuel in an oxygen-free geological repository depends on the absence of oxidizing reaction partners in the near field. This work investigates the reactions between the products of water radiolysis by alpha radiation and Fe(II) an the effect on UO2 dissolution. Solid 238PuO2 powder and UO2 pellet were allowed to react in Fe(II) solution in oxygen-free batch reactor tests and kinetics of the subsequent redox reactions were measured. Depending on the concentration of Fe(II) (tests with 10-5 and 10-4 mol L-1 were made), the induced redox reactions took place between 20 and 400 h. Dissolved uranium concentrations went first through a minimum caused by reduction, followed by a maximum caused by radiolytic oxidation, and eventually reached another minimum, probably due to sorption on precipitated Fe(III). Plutonium concentrations were decreasing steadily after going through a maximum about 70 h from the start of the experiments. The results show that in the presence of the strong alpha-radiolytic field induced by the presence of solid 238Pu, the behavior of the system is largely governed by Fe(II) as it controls the H2O2 concentration, reduces U(VI) in solution and drives the Fenton reaction leading to the oxidation of Pu(IV).

  3. PU Sizing Agent Sector Starts Reform

    Institute of Scientific and Technical Information of China (English)

    Wang Lei

    2007-01-01

    @@ Polyurethane (PU) sizing agent is a thermoplastic PU elastomer extensively used in synthetic leather, artificial deerskin and electrostatic flocking sectors. The drastic production and demand increase of synthetic leather in China in recent years has promoted rapid consumption growth of PU sizing agent.

  4. Economical Production of Pu-238

    Energy Technology Data Exchange (ETDEWEB)

    Steven D. Howe; Douglas Crawford; Jorge Navarro; Terry Ring

    2013-02-01

    All space exploration missions traveling beyond Jupiter must use radioisotopic power sources for electrical power. The best isotope to power these sources is plutonium-238. The US supply of Pu-238 is almost exhausted and will be gone within the next decade. The Department of Energy has initiated a production program with a $10M allocation from NASA but the cost is estimated at over $100 M to get to production levels. The Center for Space Nuclear Research has conceived of a potentially better process to produce Pu-238 earlier and for significantly less cost. The new process will also produce dramatically less waste. Potentially, the front end costs could be provided by private industry such that the government only had to pay for the product produced. Under a NASA Phase I NIAC grant, the CSNR has evaluated the feasibility of using a low power, commercially available nuclear reactor to produce at least 1.5 kg of Pu-238 per year. The impact on the neutronics of the reactor have been assessed, the amount of Neptunium target material estimated, and the production rates calculated. In addition, the size of the post-irradiation processing facility has been established. In addition, a new method for fabricating the Pu-238 product into the form used for power sources has been identified to reduce the cost of the final product. In short, the concept appears to be viable, can produce the amount of Pu-238 needed to support the NASA missions, can be available within a few years, and will cost significantly less than the current DOE program.

  5. Regulation of early T-lineage gene expression and developmental progression by the progenitor cell transcription factor PU.1.

    Science.gov (United States)

    Champhekar, Ameya; Damle, Sagar S; Freedman, George; Carotta, Sebastian; Nutt, Stephen L; Rothenberg, Ellen V

    2015-04-15

    The ETS family transcription factor PU.1 is essential for the development of several blood lineages, including T cells, but its function in intrathymic T-cell precursors has been poorly defined. In the thymus, high PU.1 expression persists through multiple cell divisions in early stages but then falls sharply during T-cell lineage commitment. PU.1 silencing is critical for T-cell commitment, but it has remained unknown how PU.1 activities could contribute positively to T-cell development. Here we employed conditional knockout and modified antagonist PU.1 constructs to perturb PU.1 function stage-specifically in early T cells. We show that PU.1 is needed for full proliferation, restricting access to some non-T fates, and controlling the timing of T-cell developmental progression such that removal or antagonism of endogenous PU.1 allows precocious access to T-cell differentiation. Dominant-negative effects reveal that this repression by PU.1 is mediated indirectly. Genome-wide transcriptome analysis identifies novel targets of PU.1 positive and negative regulation affecting progenitor cell signaling and cell biology and indicating distinct regulatory effects on different subsets of progenitor cell transcription factors. Thus, in addition to supporting early T-cell proliferation, PU.1 regulates the timing of activation of the core T-lineage developmental program.

  6. Pu Sorption, Desorption and Intrinsic Colloid Stability under Granitic Chemical Conditions

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Pihong [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Zavarin, Mavrik [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Dai, Zurong [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Kersting, Annie B. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2014-09-04

    This progress report (M4FT-14LL0807031) describes research conducted at LLNL as part of the Crystalline Repository effort within the UFD program. Part I describes the dissolution kinetics of intrinsic Pu colloids synthesized in an alkaline solution. Part II describes the morphology and dissolution characteristics of various forms of Pu oxides prepared over a range of solution and temperature conditions. Proposed FY15 activities are identified.

  7. Migration of plutonium from freshwater ecosystem at Hanford. [/sup 238/Pu, /sup 239/Pu, /sup 240/Pu

    Energy Technology Data Exchange (ETDEWEB)

    Emery, R. M.; Klopfer, D. C.; McShane, M. C.

    1977-09-01

    A reprocessing waste pond at Hanford has been inventoried to determine quantities of plutonium (Pu) that have been accumulated since its formation in 1944. Expressions of export were developed from these inventory data and from informed assumptions about the vectors which act to mobilize material containing Pu. This 14-acre pond provides a realistic illustration of the mobility of Pu in a lentic ecosystem. The ecological behavior of Pu in this pond is similar to that in other contaminated aquatic systems having widely differing limnological characteristics. Since its creation, this pond has received about one Ci of /sup 239/,/sup 240/Pu and /sup 238/Pu, most of which has been retained by its sediments. Submerged plants, mainly diatoms and Potamogeton, accumulate >95% of the Pu contained in biota. Emergent insects are the only direct biological route of export, mobilizing about 5 x 10/sup 3/ nCi of Pu annually, which is also the estimated maximum quantity of the Pu exported by waterfowl, birds and mammals collectively. There is no apparent significant export by wind, and it is not likely that Pu has migrated to the ground water below U-Pond via percolation. Although this pond has a rapid flushing rate, a eutrophic nutrient supply with a diverse biotic profile, and interacts with an active terrestrial environment, it appears to effectively bind Pu and prevent it from entering pathways to man and other life.

  8. A method of measurement of (239)Pu, (240)Pu, (241)Pu in high U content marine sediments by sector field ICP-MS and its application to Fukushima sediment samples.

    Science.gov (United States)

    Bu, Wenting; Zheng, Jian; Guo, Qiuju; Aono, Tatsuo; Tazoe, Hirofumi; Tagami, Keiko; Uchida, Shigeo; Yamada, Masatoshi

    2014-01-01

    An accurate and precise analytical method is highly needed for the determination of Pu isotopes in marine sediments for the long-term marine environment monitoring that is being done since the Fukushima Dai-ichi Nuclear Power Plant accident. The elimination of uranium from the sediment samples needs to be carefully checked. We established an analytical method based on anion-exchange chromatography and SF-ICP-MS in this work. A uranium decontamination factor of 2 × 10(6) was achieved, and the U concentrations in the final sample solutions were typically below 4 pg mL(-1), thus no extra correction of (238)U interferences from the Pu spectra was needed. The method was suitable for the analysis of (241)Pu in marine sediments using large sample amounts (>10 g). We validated the method by measuring marine sediment reference materials and our results agreed well with the certified and the literature values. Surface sediments and one sediment core sample collected after the nuclear accident were analyzed. The characterization of (241)Pu/(239)Pu atom ratios in the surface sediments and the vertical distribution of Pu isotopes showed that there was no detectable Pu contamination from the nuclear accident in the marine sediments collected 30 km off the plant site.

  9. The Solubility of 242PuO2 in the Presence of Aqueous Fe(II): The Impact of Precipitate Preparation

    Energy Technology Data Exchange (ETDEWEB)

    Felmy, Andrew R.; Moore, Dean A.; Buck, Edgar C.; Conradson, Steven D.; Kukkadapu, Ravi K.; Sweet, Lucas E.; Abrecht, David G.; Ilton, Eugene S.

    2014-01-28

    The solubility of different forms of precipitated 242PuO2(am) were examined in solutions containing aqueous Fe(II) over a range of pH values. The first series of 242PuO2(am) suspensions were prepared from a 242Pu(IV) stock that had been treated with thenoyltrifluoroacetone (TTA) to remove the 241Am originating from the decay of 241Pu. These 242PuO2(am) suspensions showed much higher solubilities at the same pH value and Fe(II) concentration than previous studies using 239PuO2(am). X ray absorption fine structure (XAFS) spectroscopy of the precipitates showed a substantially reduced Pu-Pu backscatter over that previously observed in 242PuO2(am) precipitates, indicating that the 242PuO2(am) precipitates purified using TTA lacked the long range order previously found in 239PuO2(am) precipitates. The Pu(IV) stock solution was subsequently repurified using an ion exchange resin and an additional series of 242PuO2(am) precipitates prepared. These suspensions showed higher redox potentials and total aqueous Pu concentrations than the TTA purified stock solution. The higher redox potential and aqueous Pu concentrations were in general agreement with previous studies on 242PuO2(am) precipitates, presumably due to the removal of possible organic compounds originally present in the TTA purified stock. 242PuO2(am) suspensions prepared with both stock solutions showed almost identical solubilities in Fe(II) containing solutions even though the initial aqueous Pu concentrations before the addition of Fe(II) were orders of magnitude different. By examining the solubility of 242PuO2(am) prepared from both stocks in this way we have essentially approached equilibrium from both the undersaturated and oversaturated

  10. The solubility of {sup 242}PuO{sub 2} in the presence of aqueous Fe(II). The impact of precipitate preparation

    Energy Technology Data Exchange (ETDEWEB)

    Felmy, Andrew R.; Moore, Dean A.; Buck, Edgar; Kukkadapu, Ravi; Sweet, Lucas; Abrecht, David; Ilton, Eugene S. [Pacific Northwest National Laboratory, Richland, WA (United States); Conrados, Steven D. [Los Alamos National Laboratory, Los Alamos, NM (United States)

    2014-07-01

    The solubility of different forms of precipitated {sup 242}PuO{sub 2}(am) were examined in solutions containing aqueous Fe(II) over a range of pH values. The first series of {sup 242}PuO{sub 2}(am) suspensions were prepared from a {sup 242}Pu(IV) stock that had been treated with thenoyltrifluoroacetone (TTA) to remove the {sup 241}Am originating from the decay of {sup 241}Pu. These {sup 242}PuO{sub 2}(am) suspensions showed much higher solubilities at the same pH value and Fe(II) concentration than previous studies using {sup 239}PuO{sub 2}(am). X-ray absorption fine structure (XAFS) spectroscopy of the precipitates showed a substantially reduced Pu-Pu backscatter over that previously observed in {sup 239}PuO{sub 2}(am) precipitates, indicating that the {sup 242}PuO{sub 2}(am) precipitates purified using TTA lacked the long range order previously found in{sup 239}PuO{sub 2}(am) precipitates. The Pu(IV) stock solution was subsequently re-purified using an ion exchange resin and an additional series of {sup 242}PuO{sub 2}(am) precipitates prepared. These suspensions showed higher redox potentials and total aqueous Pu concentrations than the TTA purified stock solution. The higher redox potential and aqueous Pu concentrations were in general agreement with previous studies on {sup 242}PuO{sub 2}(am) precipitates, presumably due to the removal of possible organic compounds originally present in the TTA purified stock. {sup 242}PuO{sub 2}(am) suspensions prepared with both stock solutions showed almost identical solubilities in Fe(II) containing solutions even though the initial aqueous Pu concentrations before the addition of Fe(II) were orders of magnitude different. By examining the solubility of {sup 242}PuO{sub 2}(am) prepared from both stocks in this way we have essentially approached equilibrium from both the undersaturated and oversaturated conditions. The final aqueous Pu concentrations are predictable using a chemical equilibrium model which includes the

  11. Simultaneous measurement of {sup 239}Pu, {sup 240}Pu, {sup 241}Pu, and {sup 242}Pu by high resolution inductively coupled plasma mass spectrometer (HR ICP-MS) in marine sediments; Mesure des isotopes du plutonium des sediments marins par spectrometrie de masse a plasma couple inductivement haute resolution (HR ICP-MS)

    Energy Technology Data Exchange (ETDEWEB)

    Bruneau, F

    1999-07-01

    Transuranics elements are of particular interest in radioecological studies because of their radiotoxicity and their potential use to decipher source fingerprints and transport processes. The simultaneous measurement of {sup 239}Pu, {sup 240}Pu, {sup 241}Pu, and {sup 242}Pu in environmental samples requires a specific chemical procedure. This work deals with an analytical procedure which yields a very high grade of purification of Pu suitable for ultra low level detection by HR ICP-MS, from marine sediments. After the elimination of major elements (Fe, Al, Mg...) by a first chromatographic separation, a new device of purification by solvent extraction and concentration by a second chromatographic separation is used to obtain a concentrated and high purified solution of plutonium. The chemical procedure have been validated on IAEA certified sediment samples and on sediment samples collected in the roads of Cherbourg which had been previously analysed by other techniques (a spectrometry and thermo-ionisation mass spectrometer). (author)

  12. Selection and Evaluation of a new Pu Density Measurement Fluid

    Energy Technology Data Exchange (ETDEWEB)

    Dziewinska, Krystyna [Los Alamos National Laboratory; Peters, Michael A [Los Alamos National Laboratory; Martinez, Patrick P [Los Alamos National Laboratory; Dziewinski, Jacek J [Los Alamos National Laboratory; Pugmire, David L [Los Alamos National Laboratory; Trujillo, Stephen M [Los Alamos National Laboratory; La Verne, Jake A [UNIV OF NOTRE DAME; Rajesh, P [UNIV OF NOTRE DAME

    2009-01-01

    This paper summarizes efforts leading to selection of a new fluid for the determination of the density of large Pu parts. Based on an extended literature search, perfluorotributylamine (FC-43) was chosen for an experimental study. Plutonium coupon corrosion studies were performed by exposing Pu to deaerated and aerated solutions and measuring corrosion gravimetrically. Corrosion rates were determined. Samples of deaerated and aerated perfuluorotributylamine (FC-43) were also irradiated with {sup 60}Co gamma rays (96 Gy/min) to various doses. The samples were extracted with NaOH and analyzed by IC and showed the presence of F and Cl{sup -}. The G-values were established. In surface study experiments Pu coupons were exposed to deaerated and aerated solutions of FC-43 and analyzed by X-ray photoelectron spectroscopy (XPS). The XPS data indicate that there is no detectable surface effect caused by the new fluid. In conclusion the FC-43 was determined to be a very effective and practical fluid for Pu density measurements.

  13. Calibration of 242 Pu Tracer by Mass Spectrometry%质谱法标定242 Pu指示剂

    Institute of Scientific and Technical Information of China (English)

    李冬梅; 徐江; 杜丽丽

    2014-01-01

    将高纯242 Pu浓度标准溶液与239 Pu混合,质谱法测量R239/242(A)先标定四水硫酸钚中239 Pu的浓度;再将四水硫酸钚与待标定的242 Pu指示剂混合,测量R239/242(A),标定242 Pu 指示剂的浓度。质谱测量还可标定得到242 Pu指示剂中的钚同位素丰度。采用两次同位素稀释质谱法标定242 Pu 指示剂快捷简便,可在2日内完成。测量精度高,242 Pu浓度的相对合成标准不确定度为0.75%,该指示剂可满足高精度分析工作的需求。%242 Pu is commonly employed as tracer for determination of 239 Pu in environmental samples.The 239 Pu concentration in Pu(SO4 )2 ·4H2 O solution was determined by isotope dilution-mass spectrometry (ID-MS)using a high pure 242 Pu spike.Then the 242 Pu tracer in our laboratary was calibrated by ID-MS using the calibrated 239 Pu solution as spike.By meas-uring the atom ratio of 239 Pu to 242 Pu twice by ID-MS,the concentration and abundance of the 242 Pu tracer in laboratary were finally calibrated.This method was proved to be efficient with high precision.The process could be finished within two days with an uncertainty of 0.75%. The calibrated 242 Pu tracer in laboratory could meet the demand of high-precision analysis.

  14. Preparation,structure and properties of porous polyimide films via PAA/PU alloy

    Institute of Scientific and Technical Information of China (English)

    LIU Jiugui; JIANG Lizhong; ZHAN Jiayu; WU Dezhen; JIN Riguang

    2007-01-01

    A new route to porous polyimide(PI)films with pore sizes in the nanometer regime was developed.A polyamic acid(PAA)/polyurethane(PU)blend with PU as the disperse phase was first prepared via in situ polymerization of pyromellitic dianhydride and 4,4-oxydianiline in PU solutions.Porous PI films were obtained from PAAJPU films by thermolysis of PU at 360℃ and imidization of PAA at 300℃,respectively.Fourier transform infrared spectroscopy and thermal gravimetric analysis were used to detect the imidization and thermolysis processes of PAA/PU blends under thermal treatment.The microporous structure of the PI films was observed by transmission electron microscopy.It was found that the size and content of pores increased with an increase in the PU mass fraction in the PAA/PU blend up to 20%.Because of the existence of nanopores,the dielectric constant of PI films decreased by a wide margin and was less than 2.0 at a PU mass fraction of 20%.It implies that this is an effective means to reduce the dielectric constant of PI,but it also causes the decrease of tensile strength and the rise of water absorption.

  15. Electronic Correlation Strength of Pu

    DEFF Research Database (Denmark)

    Svane, A.; C. Albers, R.; E. Christensen, N.

    2013-01-01

    A new electronic quantity, the correlation strength, is defined as a necessary step for understanding the properties and trends in strongly correlated electronic materials. As a test case, this is applied to the different phases of elemental Pu. Within the GW approximation we have surprisingly...... found a "universal" scaling relationship, where the f-electron bandwidth reduction due to correlation effects is shown to depend only upon the local density approximation (LDA) bandwidth and is otherwise independent of crystal structure and lattice constant....

  16. Electronic Correlation Strength of Pu

    DEFF Research Database (Denmark)

    Svane, A.; C. Albers, R.; E. Christensen, N.

    2013-01-01

    A new electronic quantity, the correlation strength, is defined as a necessary step for understanding the properties and trends in strongly correlated electronic materials. As a test case, this is applied to the different phases of elemental Pu. Within the GW approximation we have surprisingly...... found a "universal" scaling relationship, where the f-electron bandwidth reduction due to correlation effects is shown to depend only upon the local density approximation (LDA) bandwidth and is otherwise independent of crystal structure and lattice constant....

  17. Thermophysical properties and oxygen transport in the (Ux,Pu1-x)O2 lattice

    Science.gov (United States)

    Cooper, M. W. D.; Murphy, S. T.; Rushton, M. J. D.; Grimes, R. W.

    2015-06-01

    Using molecular dynamics, the thermophysical properties of the (Ux,Pu1-x)O2 system have been investigated between 300 and 3200 K. The variation with temperature of lattice parameter, linear thermal expansion coefficient, enthalpy and specific heat at constant pressure, are explained in terms of defect formation and diffusivity on the oxygen sublattice. Vegard's Law is approximately observed for the thermal expansion of the solid solutions below 2000 K. Deviation from Vegard's Law above this temperature occurs due to the different superionic transition temperatures of the solid solutions (2200-2900 K). Similarly, a spike in the specific heat, associated with the superionic transition, occurs at lower temperatures in solid solutions that have a high Pu content. While oxygen diffusivity is higher in pure PuO2 than in pure UO2, lower oxygen defect enthalpies in (Ux,Pu1-x)O2 solid solutions cause higher oxygen mobility than would be expected by interpolation between the diffusivities of the end members. In comparison to UO2 and PuO2 there is considerable variety of oxygen vacancy and oxygen interstitial sites in solid solutions generating a wide range of property values. Trends in the defect enthalpies are discussed in terms of composition and the lattice parameter of (Ux,Pu1-x)O2. Comparison is made with previous work on (Ux,Th1-x)O2.

  18. Determining Pu-239 content by resonance transmission analysis using a filtered reactor beam.

    Energy Technology Data Exchange (ETDEWEB)

    Klann, R. T.

    1998-11-25

    A novel technique has been developed at Argonne National Laboratory to determine the {sup 239}Pu content in EBR-II blanket elements using resonance transmission analysis (RTA) with a filtered reactor beam. The technique uses cadmium and gadolinium filters along with a {sup 239}Pu fission chamber to isolate the 0.3 eV resonance in {sup 239}Pu. In the energy range from 0.1 to 0.5 eV, the total microscopic cross-section of {sup 239}Pu is significantly larger than the cross-sections of {sup 238}U and {sup 235}U. This large difference in cross-section allows small amounts of {sup 239}Pu to be detected in uranium samples. Tests using a direct beam from a 250 kW TRIGA reactor have been performed with stacks of depleted uranium and {sup 239}Pu foils. Preliminary measurement results are in good agreement with the predicted results up to about two weight percent of {sup 239}Pu in the sample. In addition, measured {sup 239}Pu masses were in agreement with actual sample masses with uncertainties less than 3.8 percent.

  19. Reduction of Pu(VI) on Fe surfaces: soft x-ray absorption and resonant inelastic scattering study

    Energy Technology Data Exchange (ETDEWEB)

    Butorin, S.M.; Kvashnina, K.O.; Modin, A.; Nordgren, J. (Dept. of Physics and Materials Science, Uppsala Univ., Uppsala (Sweden)); Guo, J.H. (Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA (United States)); Shuh, D.K. (Chemical Science Div., Lawrence Berkeley National Laboratory, Berkeley, CA (United States)); Werme, L. (Swedish Nuclear Fuel and Waste Management Co., Stockholm (Sweden))

    2009-03-15

    Based on analysis of spectral shapes, their dependence on the energy of incident photons and comparison with model calculations and experimental data from the reference sample we can conclude that plutonium from the Pu(VI) solution sorbed on Fe surfaces is likely to be reduced and Pu species sorbed on the Fe foils are mainly in the form of Pu (IV). Current results correlate with what was observed for for Np (V) and U (VI) in our previous studies. Furthermore, combined analysis of present data with model atomic multiplet calculations of RIXS and XAS spectra suggests that significant presence of Pu(III) on the Fe foils is unlikely

  20. DETERMINATION OF 237NP AND PU ISOTOPES IN LARGE SOIL SAMPLES BY INDUCTIVELY COUPLED PLASMA MASS SPECTROMETRY

    Energy Technology Data Exchange (ETDEWEB)

    Maxwell, S.

    2010-07-26

    A new method for the determination of {sup 237}Np and Pu isotopes in large soil samples has been developed that provides enhanced uranium removal to facilitate assay by inductively coupled plasma mass spectrometry (ICP-MS). This method allows rapid preconcentration and separation of plutonium and neptunium in large soil samples for the measurement of {sup 237}Np and Pu isotopes by ICP-MS. {sup 238}U can interfere with {sup 239}Pu measurement by ICP-MS as {sup 238}UH{sup +} mass overlap and {sup 237}Np via {sup 238}U peak tailing. The method provides enhanced removal of uranium by separating Pu and Np initially on TEVA Resin, then transferring Pu to DGA resin for additional purification. The decontamination factor for removal of uranium from plutonium for this method is greater than 1 x 10{sup 6}. Alpha spectrometry can also be applied so that the shorter-lived {sup 238}Pu isotope can be measured successfully. {sup 239}Pu, {sup 242}Pu and {sup 237}Np were measured by ICP-MS, while {sup 236}Pu and {sup 238}Pu were measured by alpha spectrometry.

  1. Heterogeneous Reduction of PuO2 with Fe(II): Importance of the Fe(III) Reaction Product

    Energy Technology Data Exchange (ETDEWEB)

    Felmy, Andrew R.; Moore, Dean A.; Rosso, Kevin M.; Qafoku, Odeta; Rai, Dhanpat; Buck, Edgar C.; Ilton, Eugene S.

    2011-05-01

    Abstract Heterogeneous reduction of actinides in higher and more soluble oxidation states to lower more insoluble oxidation states by reductants such as Fe(II) has been the subject of intensive study for more than two decades. However, Fe(II)-induced reduction of sparingly soluble Pu(IV) to the more soluble lower oxidation state Pu(III) has been much less studied even though such reactions can potentially increase the mobility of Pu in the subsurface. Thermodynamic calculations are presented that show how differences in the free energy of various possible solid-phase Fe(III) reaction products can greatly influence aqueous Pu(III) concentrations resulting from reduction of PuO2(am) by Fe(II). We present the first experimental evidence that reduction of PuO2(am) to Pu(III) by Fe(II) was enhanced when the Fe(III) mineral goethite was spiked into the reaction. The effect of goethite on reduction of Pu(IV) was demonstrated by measuring the time-dependence of total aqueous Pu concentration, its oxidation state, and system pe/pH. We also re-evaluated established protocols for determining Pu(III) [(Pu(III) + Pu(IV)) - Pu(IV)] by using thenoyltrifluoroacetone (TTA) in toluene extractions; the study showed that it is important to eliminate dissolved oxygen from the TTA solutions for accurate determinations. More broadly, this study highlights the importance of the Fe(III) reaction product in actinide reduction rate and extent by Fe(II).

  2. Adsorption of Atmospheric Gases on Pu Surfaces

    Energy Technology Data Exchange (ETDEWEB)

    Nelson, A J; Holliday, K S; Stanford, J A; Grant, W K; Erler, R G; Allen, P G; McLean, W; Roussel, P

    2012-03-29

    Surface adsorption represents a competition between collision and scattering processes that depend on surface energy, surface structure and temperature. The surface reactivity of the actinides can add additional complexity due to radiological dissociation of the gas and electronic structure. Here we elucidate the chemical bonding of gas molecules adsorbed on Pu metal and oxide surfaces. Atmospheric gas reactions were studied at 190 and 300 K using x-ray photoelectron spectroscopy. Evolution of the Pu 4f and O 1s core-level states were studied as a function of gas dose rates to generate a set of Langmuir isotherms. Results show that the initial gas dose forms Pu{sub 2}O{sub 3} on the Pu metal surface followed by the formation of PuO{sub 2} resulting in a layered oxide structure. This work represents the first steps in determining the activation energy for adsorption of various atmospheric gases on Pu.

  3. Leukemogenesis in heterozygous PU.1 knockout mice.

    Science.gov (United States)

    Genik, Paula C; Vyazunova, Irina; Steffen, Leta S; Bacher, Jeffery W; Bielefeldt-Ohmann, Helle; McKercher, Scott; Ullrich, Robert L; Fallgren, Christina M; Weil, Michael M; Ray, F Andrew

    2014-09-01

    Most murine radiation-induced acute myeloid leukemias involve biallelic inactivation of the PU.1 gene, with one allele being lost through a radiation-induced chromosomal deletion and the other allele affected by a recurrent point mutation in codon 235 that is likely to be spontaneous. The short latencies of acute myeloid leukemias occurring in nonirradiated mice engineered with PU.1 conditional knockout or knockdown alleles suggest that once both copies of PU.1 have been lost any other steps involved in leukemogenesis occur rapidly. Yet, spontaneous acute myeloid leukemias have not been reported in mice heterozygous for a PU.1 knockout allele, an observation that conflicts with the understanding that the PU.1 codon 235 mutation is spontaneous. Here we describe experiments that show that the lack of spontaneous leukemia in PU.1 heterozygous knockout mice is not due to insufficient monitoring times or mouse numbers or the genetic background of the knockout mice. The results reveal that spontaneous leukemias that develop in mice of the mixed 129S2/SvPas and C57BL/6 background of knockout mice arise by a pathway that does not involve biallelic PU.1 mutation. In addition, the latency of radiation-induced leukemia in PU.1 heterozygous mice on a genetic background susceptible to radiation-induced leukemia indicates that the codon 235 mutation is not a rate-limiting step in radiation leukemogenesis driven by PU.1 loss.

  4. Determination of plutonium isotopes (238Pu, 239Pu, 240Pu, 241Pu) in environmental samples using radiochemical separation combined with radiometric and mass spectrometric measurements

    DEFF Research Database (Denmark)

    Xu, Yihong; Qiao, Jixin; Hou, Xiaolin

    2014-01-01

    This paper reports an analytical method for the determination of plutonium isotopes (238Pu, 239Pu, 240Pu, 241Pu) in environmental samples using anion exchange chromatography in combination with extraction chromatography for chemical separation of Pu. Both radiometric methods (liquid scintillation...

  5. New measurement of the 242Pu(n,γ) cross section at n_TOF

    OpenAIRE

    Lerendegui-Marco J.; Guerrero C.; Cortés-Giraldo M. A.; Quesada J.M.; Mendoza E.; Cano-Ott D.; Eberhardt K.; Junghans A.

    2016-01-01

    WONDER-2015 – 4th International Workshop On Nuclear Data Evaluation for Reactor applications The use of MOX fuel (mixed-oxide fuel made of UO2 and PuO2) in nuclear reactors allows substituting a large fraction of the enriched Uranium by Plutonium reprocessed from spent fuel. With the use of such new fuel composition rich in Pu, a better knowledge of the capture and fission cross sections of the Pu isotopes becomes very important. In particular, a new series of cross section evaluations hav...

  6. Potential of Vetiveria zizanoides L. Nash for phytoremediation of plutonium ((239)Pu): Chelate assisted uptake and translocation.

    Science.gov (United States)

    Singh, Shraddha; Fulzele, D P; Kaushik, C P

    2016-10-01

    Plants have demonstrated a great potential to remove toxic elements from soils and solutions and been successfully used for phytoremediation of important radionuclides. Uptake potential of vetiver plants (V. zizanoides) for the remediation of (239)Pu in hydroponic and soil conditions was studied in the present work. High efficiency of V. zizanoides for the removal of (239)Pu was recorded with 66.2% being removed from the hydroponic solution after 30 days. However, remediation of (239)Pu from soil was limited. Remediation of (239)Pu from soil was increased with the addition of chelating agents citric acid (CA) and diethylenetriaminepentaacetic acid (DTPA). Accumulation of (239)Pu was recorded higher in roots than shoots, however its translocation from roots to shoots increased in the presence of chelators in hydroponic as well as soil conditions. DTPA was found more effective than CA showing higher translocation index (TI). Increase in TI was observed 8 and 6 times in the solution and soil respectively when plants were exposed to (239)Pu-DTPA in comparison to only (239)Pu. The present study demonstrates that V. zizanoides plant is a potential plant for phytoremediation of (239)Pu. Copyright © 2016 Elsevier Inc. All rights reserved.

  7. Radionuclide release from irradiated Th-Pu mox fuel

    Energy Technology Data Exchange (ETDEWEB)

    Rodriguez, N.; Quinones, J. [Ciemat., Avda. Complutense 22. E-28040 Madrid (Spain); Cobos, J. [Centro Nacional de Aceleradores, Parque Tecnologico Cartuja 93, Av. Thomas Alva Edison, 7, E-41092 Sevilla (Spain); Rondinella, V.V.; Van Winckel, S.; Somers, J.; Papaioanu, D.; Glatz, J.P. [European Commission, Joint Research Centre, Institute for Transuranium Elements, Postfach 2340, D-76125 Karlsruhe (Germany)

    2010-07-01

    Plutonium and minor actinides produced as by-products of the UO{sub 2} nuclear cycle could be considered as waste or energy source depending on the strategy selected in the nuclear energy programme. Considering Pu and Minor Actinides as a source, they can be burned in existing water reactor for diminishing the radiotoxicity of the spent fuel, it is necessary to use 'inactive' materials as matrix like ThO{sub 2}. ThO{sub 2} matrix has demonstrated its Pu burning efficiency and higher corrosion resistance than UO{sub 2}. Uranium-plutonium mixed oxide (MOX) fuel efficiency is low because the presence of U in MOX results in the creation of some new Pu under irradiation. The dissolution behaviour of irradiated (Th,Pu)O{sub 2} pellets with burn-up of 38.8 MWd/kg Th has been studied in carbonated (20 mM HCO{sub 3}{sup -}), deionised and granite ground water solution in a hot cell. The dissolution behaviour of Th, Pu, U and Np was studied in order to find out whether radionuclides release is depending on the matrix dissolution (solubility control). After irradiating the samples, K-ORIGEN and ORIGEN ARP codes were used to find out the theoretical inventory. Afterwards, fuel samples were dissolved completely and analyzed, in order to determine the experimental radionuclide inventory of the irradiated fuel. Th matrix alteration appears to reach an steady state and radionuclides dissolution shows dependence on the matrix behaviour as can be observed through the FIAP results. (authors)

  8. Analysis of plutonium isotope ratios including (238)Pu/(239)Pu in individual U-Pu mixed oxide particles by means of a combination of alpha spectrometry and ICP-MS.

    Science.gov (United States)

    Esaka, Fumitaka; Yasuda, Kenichiro; Suzuki, Daisuke; Miyamoto, Yutaka; Magara, Masaaki

    2017-04-01

    Isotope ratio analysis of individual uranium-plutonium (U-Pu) mixed oxide particles contained within environmental samples taken from nuclear facilities is proving to be increasingly important in the field of nuclear safeguards. However, isobaric interferences, such as (238)U with (238)Pu and (241)Am with (241)Pu, make it difficult to determine plutonium isotope ratios in mass spectrometric measurements. In the present study, the isotope ratios of (238)Pu/(239)Pu, (240)Pu/(239)Pu, (241)Pu/(239)Pu, and (242)Pu/(239)Pu were measured for individual Pu and U-Pu mixed oxide particles by a combination of alpha spectrometry and inductively coupled plasma mass spectrometry (ICP-MS). As a consequence, we were able to determine the (240)Pu/(239)Pu, (241)Pu/(239)Pu, and (242)Pu/(239)Pu isotope ratios with ICP-MS after particle dissolution and chemical separation of plutonium with UTEVA resins. Furthermore, (238)Pu/(239)Pu isotope ratios were able to be calculated by using both the (238)Pu/((239)Pu+(240)Pu) activity ratios that had been measured through alpha spectrometry and the (240)Pu/(239)Pu isotope ratios determined through ICP-MS. Therefore, the combined use of alpha spectrometry and ICP-MS is useful in determining plutonium isotope ratios, including (238)Pu/(239)Pu, in individual U-Pu mixed oxide particles. Copyright © 2016 Elsevier B.V. All rights reserved.

  9. Study of Removal Nitrous Acid From Nitric Acid Solution Using Packed Column

    Institute of Scientific and Technical Information of China (English)

    LAN; Tian; CHANG; Shang-wen; LIU; Jin-ping; ZHOU; Xian-ming; LI; Gao-liang; TANG; Hong-bin; HE; Hui

    2013-01-01

    It is necessary that the adjustment of the Pu(Ⅲ)to Pu(Ⅳ)should be used excess nitride gases befor the cycle of Pu purification in Purex.The mass of nitrous acid were present in solution after adjustment.Ifthe solution contain the mass of nitrous acid arrived at the cycle of Pupurification,the nitrous could react with Pu reducing agent in the processof Pu back-extractionbecause nitrous acid could extracted to organic,

  10. Probing the Pu4 + magnetic moment in PuF4 with 19F NMR spectroscopy

    Science.gov (United States)

    Capan, Cigdem; Dempsey, Richard J.; Sinkov, Sergey; McNamara, Bruce K.; Cho, Herman

    2016-06-01

    The magnetic fields produced by Pu4 + centers have been measured by 19F NMR spectroscopy to elucidate the Pu-F electronic interactions in polycrystalline PuF4. Spectra acquired at applied fields of 2.35 and 7.05 T reveal a linear scaling of the 19F line shape. A model is presented that treats the line broadening and shifts as due to dipolar fields produced by Pu valence electrons in localized noninteracting orbitals. Alternative explanations for the observed line shape involving covalent Pu-F bonding, superexchange interactions, and electronic configurations with enhanced magnetic moments are considered.

  11. Development of the DGT technique for in-situ Pu speciation measurements

    Energy Technology Data Exchange (ETDEWEB)

    Cusnir, R.; Bochud, F.; Froidevaux, P. [Institute of Radiation Physics, Lausanne University Hospital, Rue du Grand-Pre 1, CH-1007 Lausanne (Switzerland); Steinmann, P. [Federal Office of Public Health, Swarzenburgstrasse 165, CH-3003 Bern (Switzerland)

    2014-07-01

    Toxic effects of artificial radionuclides are strongly dependent on the surrounding chemical environment which determines the bioavailability of contaminant species. Speciation of plutonium in the environment is of particular interest since it is a long-life actinide contributing to the dose exposure via ingestion with water and food in case of radioactive discharge. Furthermore, natural colloids present in waters, as main carriers of dissolved trace metals, can transport plutonium over significant distances from contaminated sites. The diffusive gradients in thin films (DGT) technique is an efficient instrument for passive sampling of trace metals. It allows for in-situ monitoring of mean concentrations of bioavailable contaminant species (1). A DGT sampler consists of two gel layers: a polyacrylamide hydrogel diffusion layer allowing to diffuse labile metal species to the second, binding layer, impregnated with ion-exchange resin. Resin elution and further analysis allow determining the amount of the bioavailable fraction of trace metals in the bulk solution, which can be calculated from the relationship: C{sub bulk}= (M x Δg)/(D x t x A) where M is the measured metal species inventory in the resin, Δg the thickness of the diffusion layer, D the diffusion coefficient of the species in the gel, t the time of deployment, A the diffusion area. To our knowledge, the DGT has not yet been applied for Pu speciation measurements and the D value is unknown. Here we propose the use of DGT to monitor the dissolved phase and labile complexes of plutonium in the aquatic environment. We have first measured the diffusion coefficient of plutonium in the hydrogel. Experiments were carried out in a diffusion cell (2) and with commercially available DGT samplers exposed in standardized solutions containing {sup 239}Pu at pico-molar concentrations. Both approaches give comparable D values in the range of 2.30 x 10{sup -6} - 2.45 x 10{sup -6} cm{sup 2} s{sup -1}. We then studied

  12. The uptake of Cs, Cl, I, Co, U and Pu by C-S-H, portlandite and ettringite

    Energy Technology Data Exchange (ETDEWEB)

    Le Callonnec, C.; Richet, C.; Ayache, R

    2000-07-01

    The aim of this work is to study the retention of Pu, Cs, Cl, U, Co and I onto the three phases of a cement paste: calcium silicate hydrates or C-S-H (Ca/Si=1.65), portlandite (Ca(OH){sub 2}) and ettringite (Ca{sub 6}Al{sub 2}S{sub 3}O{sub 21}.32H{sub 2}O). C-S-H of Ca/Si molar ratio of 1.65 and ettringite were prepared in suspension, while portlandite was provided by an industrial laboratory. The sorptive power for each ion was determined by a batch model at 20 degrees Celsius. The uptake of ions onto the phases has been obtained by introducing a very small volume of radioactive Cs, Co, Cl, I, U and Pu solution in each batch. Aliquots of solution were periodically removed for analysis. The results show that there are two kinds of ions whatever the solid phase: those which are poorly sorbed: Cs, Cl, I and Co, U and Pu which are strongly sorbed (by a factor 100 to 10000). Elsewhere, the comparison between the sorptive power of each phase reveals that C-S-H develops a significant sorption potential for pluri-valent ions (Pu, U, Co) as well as for Cl. The retention capacity of portlandite mainly towards pluri-valent cations is one or two orders of magnitude weaker than C-S-H capacity. Ettringite only plays a sorptive role relatively to Cs. However, iodine does not have a strong affinity for any solid at all. The data allow us to calculate a global sorption coefficient Kd of the cement paste for each ion. Assuming that the proportion of C-S-H, portlandite, ettringite is respectively 65%, 15% and 5% in a Portland cement, the global sorption coefficient is in good agreement with literature regarding on U, Cs, I and Cl. Cementitious materials appear to be an interesting chemical barrier that can limit the diffusion of pluri-valent cations. As C-S-H represent from 60% to 75% of the cement paste, this study leads to underline that C-S-H is mainly responsible for the retention capacity of cementitious materials specially towards U, Pu, Co, Cl although its sorption power is

  13. Experimental Limit to Interstellar 244Pu Abundance

    CERN Document Server

    Paul, M; Ahmad, I; Berkovits, D; Bordeanu, C; Ghelberg, S; Hashimoto, Y; Hershcovitch, A I; Jiang, S; Nakanishi, T; Sakamoto, K

    2001-01-01

    Short-lived nuclides, now extinct in the solar system, are expected to be present in the interstellar medium (ISM). Grains of ISM origin were recently discovered in the inner solar system and at Earth orbit and may accrete onto Earth after ablation in the atmosphere. A favorable matrix for detection of such extraterrestrial material is presented by deep open-sea sediments with very low sedimentation rates (0.8-3 mm/kyr). We report here on the measurement of Pu isotopic abundances in a 1-kg deep-sea dry sediment collected in 1992 in the North Pacific. Our measured value of (3+-3)x10^5 244Pu atoms in the Pu-separated fraction of the sample shows no excess over the expected stratospheric nuclear fallout content and under reasonable assumptions we derive a limit of 2x10^-11 g-244Pu/g-ISM for the abundance of 244Pu in ISM.

  14. Observations of surface-mediated reduction of Pu(VI) to Pu(IV) on hematite nanoparticles by ATR FT-IR

    Energy Technology Data Exchange (ETDEWEB)

    Emerson, Hilary P. [Florida International Univ., Applied Research Center, Miami, FL (United States); Powell, Brian A. [Clemson Univ., Dept. of Enviromental Engineering and Earth Sciences, Anderson, SC (United States)

    2015-07-01

    Previous studies have shown that mineral surfaces may facilitate the reduction of plutonium though the mechanisms of the reduction are still unknown. The objective of this study is to use batch sorption and attenuated total reflectance Fourier transform infrared spectroscopy experiments to observe the surface-mediated reduction of plutonium on hematite nanoparticles. These techniques allow for in situ measurement of reduction of plutonium with time and may lead to a better understanding of the mechanisms of surface mediated reduction of plutonium. For the first time, ATR FT-IR peaks for Pu(VI) sorbed to hematite are measured at ∝ 916 cm{sup -1}, respectively. The decrease in peak intensity with time provides a real-time, direct measurement of Pu(VI) reduction on the hematite surface. In this work pseudo first order rate constants estimated at the high loadings (22 mg{sub Pu}/g{sub hematite}, 1.34 x 10{sup -6} M{sub Pu}/m{sup 2}) for ATR FT-IR are approximately 10 x slower than at trace concentrations based on previous work. It is proposed that the reduced rate constant at higher Pu loadings occurs after the reduction capacity due to trace Fe(II) has been exhausted and is dependent on the oxidation of water and possibly electron shuttling based on the semiconducting nature of hematite. Therefore, the reduction rate at higher loadings is possibly due to the thermodynamic favorability of Pu(IV)-hydroxide complexes.

  15. Direct isotope ratio analysis of individual uranium-plutonium mixed particles with various U/Pu ratios by thermal ionization mass spectrometry.

    Science.gov (United States)

    Suzuki, Daisuke; Esaka, Fumitaka; Miyamoto, Yutaka; Magara, Masaaki

    2015-02-01

    Uranium and plutonium isotope ratios in individual uranium-plutonium (U-Pu) mixed particles with various U/Pu atomic ratios were analyzed without prior chemical separation by thermal ionization mass spectrometry (TIMS). Prior to measurement, micron-sized particles with U/Pu ratios of 1, 5, 10, 18, and 70 were produced from uranium and plutonium certified reference materials. In the TIMS analysis, the peaks of americium, plutonium, and uranium ion signals were successfully separated by continuously increasing the evaporation filament current. Consequently, the uranium and plutonium isotope ratios, except the (238)Pu/(239)Pu ratio, were successfully determined for the particles at all U/Pu ratios. This indicates that TIMS direct analysis allows for the measurement of individual U-Pu mixed particles without prior chemical separation.

  16. Radiolysis and corrosion of 238Pu-doped UO2 pellets in chloride brine

    Indian Academy of Sciences (India)

    M Kelm; E Bohnert

    2002-12-01

    Deaerated 5 M NaCl solution is irradiated in the presence of UO2 pellets with a-radiation from 238Pu. Experiments are conducted with 238Pu doped pellets and others with 238Pu dissolved in the brine. The radiolysis products and yields of mobilized U and Pu from the oxidative dissolution of UO2 are determined. Results found for radiolysis products and for the oxidation/dissolution of pellets immersed in Pu containing brine are similar to results for Pu doped pellets, where the radiation chemical processes occur only in the liquid layer of some 10 m thickness adjacent to the pellet. The yield of radiolysis products is comparable to earlier results, that of mobilized U from the pellets is < 1% of the total amount of oxidized species. Thus, the radiation chemical yield (-value) for mobilized hexavalent U is < 0.01 ions/100 eV. In spite of the low radiation yield for the corrosion, the rate of UO2 dissolution is higher than expected for the concentrations of long-lived oxidizing radiolysis compounds found in the solutions.

  17. Chemically selective polymer substrate based direct isotope dilution alpha spectrometry of Pu.

    Science.gov (United States)

    Paul, Sumana; Pandey, Ashok K; Shah, R V; Aggarwal, S K

    2015-06-01

    Quantification of actinides in the complex environmental, biological, process and waste streams samples requires multiple steps like selective preconcentration and matrix elimination, solid source preparations generally by evaporation or electrodeposition, and finally alpha spectrometry. To minimize the sample manipulation steps, a membrane based isotope dilution alpha spectrometry method was developed for the determination of plutonium concentrations in the complex aqueous solutions. The advantages of this method are that it is Pu(IV) selective at 3M HNO3, high preconcentration factor can be achieved, and obviates the need of solid source preparation. For this, a thin phosphate-sulfate bifunctional polymer layer was anchored on the surface of microporous poly(ethersulfone) membrane by UV induced surface grafting. The thickness of the bifunctional layer on one surface of the poly(ethersulfone) membrane was optimized. The thickness, physical and chemical structures of the bifunctional layer were studied by secondary ionization mass spectrometry (SIMS), scanning electron microscopy (SEM) and SEM-EDS (energy-dispersive spectroscopy). The optimized membrane was used for preconcentration of Pu(IV) from aqueous solutions having 3-4M HNO3, followed by direct quantification of the preconcentrated Pu(IV) by isotope dilution alpha spectrometry using (238)Pu spike. The chemical recovery efficiency of Pu(IV) was found to be 86±3% below Pu(IV) loading capacity (1.08 μg in 2×1 cm(2)) of the membrane sample. The experiments with single representative actinides indicated that Am(III) did not sorb to significant extent (7%) but U(VI) sorbed with 78±3% efficiency from the solutions having 3M HNO3 concentration. However, Pu(IV) chemical recovery in the membrane remained unaffected from the solution containing 1:1000 wt. proportion of Pu(IV) to U(VI). Pu concentrations in the (U, Pu)C samples and in the irradiated fuel dissolver solutions were determined. The results thus obtained

  18. The electrical resistance of PuSb under high pressure

    Energy Technology Data Exchange (ETDEWEB)

    Link, P. (European Commission, Joint Research Centre, Institute for Transuranium Elements, Postfach 2340, D76125 Karlsruhe (Germany)); Benedict, U. (European Commission, Joint Research Centre, Institute for Transuranium Elements, Postfach 2340, D76125 Karlsruhe (Germany)); Wittig, J. (Institut fuer Festkoerperforschung, Forschungszentrum Juelich, D52425 Juelich (Germany)); Wuehl, H. (Institut fuer Experimentelle Kernphysik, Universitaet Karlsruhe, D76128 Karlsruhe (Germany)); Rebizant, J. (European Commission, Joint Research Centre, Institute for Transuranium Elements, Postfach 2340, D76125 Karlsruhe (Germany)); Spirlet, J.C. (European Commission, Joint Research Centre, Institute for Transuranium Elements, Postfach 2340, D76125 Karlsruhe (Germany))

    1994-10-01

    A new experimental set-up with a Bridgman-type high pressure cell in a closed containment allows resistance measurements on highly radioactive materials. We present results of high pressure, low temperature studies on PuSb single crystals in the pressure range to 25 GPa and at temperatures between 1.3 K and 300 K. As pressure on PuSb is increased, its Neel temperature and the transition temperature to the ferromagnetic ground state are increased. In the pressure range from 10 to 15 GPa, we observed a strong decrease in the resistance associated with the crystallographic phase transition from the B1 (NaCl) to the B2 (CsCl) structure. The high pressure phase appears to be non-magnetic. ((orig.))

  19. District energy: an important factor in the socially and environmentally responsible solution for the electric power industry; (requiring greater accelerated capital cost allowance treatment for income tax purposes)

    Energy Technology Data Exchange (ETDEWEB)

    Boucher, P. [HSBC James Capel Canada Inc. (Canada); Stevens, S. [Business Development Consumers Utilities (Canada)

    1996-09-01

    The considerable amount of risk associated with the investment in district energy systems was discussed. It was explained that district energy projects frequently require additional capital allowances, particularly in the initial years of a typical project, in order to attract private capital investments to the industry. Advantages of district energy systems were reviewed, among them reduction in CO{sub 2} and NO{sub x} emissions, enhancing energy conservation through the use of high efficiency boilers or thermal waste energy, increasing tax revenue at various levels of government, providing much-needed capital injection into communities, providing construction and operation jobs, and allowing electric utilities to offer cogeneration from older plants helping to avoid stranded investments. 1 tab.

  20. Physical and economical aspects of Pu multiple recycling on the basis of REMIX reprocessing technology in thermal reactors

    Directory of Open Access Journals (Sweden)

    Teplov Pavel S.

    2016-01-01

    Full Text Available The basic strategy of Russian nuclear energy is propagation of a closed fuel cycle on the basis of fast breeder and thermal reactors, as well as the solution of the spent nuclear fuel accumulation and resource problems. The three variants of multiple Pu and U recycling in Russian pressurized water reactor concept reactors on the basis of REgenerated MIXture of U, Pu oxides (REMIX reprocessing technology are considered in this work. The REMIX fuel is fabricated from an unseparated mixture of uranium and plutonium obtained during spent fuel reprocessing with further makeup by enriched natural U or reactor grade Pu. This makes it possible to recycle several times the total amount of Pu obtained from the spent fuel. The main difference in Pu recycling is the concept of 100% or partial fuel loading of the core. The third variant is heterogeneous composition of enriched uranium and uranium–plutonium mixed oxide fuel pins in one fuel assembly. It should be noted that all fuel assemblies with Pu require the involvement of expensive technologies during manufacturing. These three variants of the full core loadings can be balanced on zero Pu accumulation in the cycle. The various physical and economical aspects of Pu and U multiple recycling in selected variants are observed in the given work.

  1. Study on Fluorescence Analytical Method of Micro Th in Pu

    Institute of Scientific and Technical Information of China (English)

    QIAN; Hong-juan; ZHANG; Li-hua; LIU; Huan-liang; FAN; De-jun

    2013-01-01

    As one of impurities,Th is needed to be determined for control quality of Pu product.Due to the high radioactivity and fatal toxicity of Pu,it is very difficult to measure the micro Th in Pu product.It is necessary to develop a sensitive method for determining the micro Th in Pu under the described harsh condition.

  2. Measurement of the ${240}$Pu(n,f) reaction cross-section

    CERN Multimedia

    Following proposal CERN-INTC-2010-042 / INTC-P-280 (“Measurement of the fission cross-section of $^{240}$Pu and $^{242}$Pu at CERN’s n_TOF Facility”), the parallel measurement of the $^{240}$Pu(n,f) and $^{242}$Pu(n,f) reaction cross-sections was carried out at n_TOF EAR-1. While the $^{242}$Pu measurement was successful, unexpected sample-induced damage to the detectors caused by the high α-activity of the 240Pu samples resulted in a deterioration of the detector performance over the data taking period of several months, which compromised the measurement. This obstacle can be eliminated by performing the measurement in EAR-2, where the higher neutron flux will allow collecting data in a much shorter time, thus preventing the degradation of the detectors. In addition to this obvious advantage, the measurement would also benefit from the stronger suppression of the sample-induced α-background, due to the shorter times-of-flight involved.

  3. SOLUTIONING

    Directory of Open Access Journals (Sweden)

    Maria de Hoyos Guajardo, Ph.D. Candidate, M.Sc., B.Eng.

    2004-11-01

    Full Text Available The theory that is presented below aims to conceptualise how a group of undergraduate students tackle non-routine mathematical problems during a problem-solving course. The aim of the course is to allow students to experience mathematics as a creative process and to reflect on their own experience. During the course, students are required to produce a written ‘rubric’ of their work, i.e., to document their thoughts as they occur as well as their emotionsduring the process. These ‘rubrics’ were used as the main source of data.Students’ problem-solving processes can be explained as a three-stage process that has been called ‘solutioning’. This process is presented in the six sections below. The first three refer to a common area of concern that can be called‘generating knowledge’. In this way, generating knowledge also includes issues related to ‘key ideas’ and ‘gaining understanding’. The third and the fourth sections refer to ‘generating’ and ‘validating a solution’, respectively. Finally, once solutions are generated and validated, students usually try to improve them further before presenting them as final results. Thus, the last section deals with‘improving a solution’. Although not all students go through all of the stages, it may be said that ‘solutioning’ considers students’ main concerns as they tackle non-routine mathematical problems.

  4. Aqueous Solution Chemistry of Plutonium

    Energy Technology Data Exchange (ETDEWEB)

    Clark, David L. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2014-01-28

    Things I have learned working with plutonium: Chemistry of plutonium is complex; Redox equilibria make Pu solution chemistry particularly challenging in the absence of complexing ligands; Understanding this behavior is key to successful Pu chemistry experiments; There is no suitable chemical analog for plutonium.

  5. Improved MOX fuel calculations using new Pu-239, Am-241 and Pu-240 evaluations

    Science.gov (United States)

    Noguere, G.; Bouland, O.; Bernard, D.; Leconte, P.; Blaise, P.; Peneliau, Y.; Vidal, J. F.; De Saint Jean, C.; Leal, L.; Schillebeeckx, P.; Kopecky, S.; Lampoudis, C.

    2013-03-01

    Several studies based on the JEFF-3.1.1 nuclear data library show a systematic overestimation of the critical keff for core configurations of MOX fuel assemblies. The present work investigates possible improvements of the C/E results by using new evaluations for Am-241, Pu-239 and Pu-240.

  6. Improved MOX fuel calculations using new Pu-239, Am-241 and Pu-240 evaluations

    Directory of Open Access Journals (Sweden)

    Schillebeeckx P.

    2013-03-01

    Full Text Available Several studies based on the JEFF-3.1.1 nuclear data library show a systematic overestimation of the critical keff for core configurations of MOX fuel assemblies. The present work investigates possible improvements of the C/E results by using new evaluations for Am-241, Pu-239 and Pu-240.

  7. A multi-radionuclide approach to evaluate the suitability of (239+240)Pu as soil erosion tracer.

    Science.gov (United States)

    Meusburger, Katrin; Mabit, Lionel; Ketterer, Michael; Park, Ji-Hyung; Sandor, Tarjan; Porto, Paolo; Alewell, Christine

    2016-10-01

    Fallout radionuclides have been used successfully worldwide as tracers for soil erosion, but relatively few studies exploit the full potential of plutonium (Pu) isotopes. Hence, this study aims to explore the suitability of the plutonium isotopes (239)Pu and (240)Pu as a method to assess soil erosion magnitude by comparison to more established fallout radionuclides such as (137)Cs and (210)Pbex. As test area an erosion affected headwater catchment of the Lake Soyang (South Korea) was selected. All three fallout radionuclides confirmed high erosion rates for agricultural sites (>25tha(-1)yr(-1)). Pu isotopes further allowed determining the origin of the fallout. Both (240)Pu/(239)Pu atomic ratios and (239+240)Pu/(137)Cs activity ratios were close to the global fallout ratio. However, the depth profile of the (239+240)Pu/(137)Cs activity ratios in undisturbed sites showed lower ratios in the top soil increments, which might be due to higher migration rates of (239+240)Pu. The activity ratios further indicated preferential transport of (137)Cs from eroded sites (higher ratio compared to the global fallout) to the depositional sites (smaller ratio). As such the (239+240)Pu/(137)Cs activity ratio offered a new approach to parameterize a particle size correction factor that can be applied when both (137)Cs and (239+240)Pu have the same fallout source. Implementing this particle size correction factor in the conversion of (137)Cs inventories resulted in comparable estimates of soil loss for (137)Cs and (239+240)Pu. The comparison among the different fallout radionuclides highlights the suitability of (239+240)Pu through less preferential transport compared to (137)Cs and the possibility to gain information regarding the origin of the fallout. In conclusion, (239+240)Pu is a promising soil erosion tracer, however, since the behaviour i.e. vertical migration in the soil and lateral transport during water erosion was shown to differ from that of (137)Cs, there is a clear

  8. Sorption Distribution Coefficient of Pu (Ⅳ) and Pu (Ⅴ) in Sand Soil%Pu(Ⅳ)、Pu(Ⅴ)在不同质地砂土中的分配

    Institute of Scientific and Technical Information of China (English)

    于静; 司高华; 黄云贵; 刘东旭

    2011-01-01

    Pu(Ⅲ)、Pu(Ⅳ)、Pu(Ⅴ)和Pu(Ⅵ)在自然水的pH和Eh(氧化还原电势)值范围内能够共存.在自然环境中主要以Pu(Ⅴ)的PuO2(H2O)n+和Pu(Ⅳ)的Pu(OH)4形式存在.采用静态法测定了Pu(Ⅳ)和Pu(Ⅴ)在砂土介质中的分配系数Kd,Pu(Ⅳ)和Pu(Ⅴ)在砂土中的分配系数范围分别为5.5×103~4×104mL/g和3.2×103~1.1×104mL/g.表明在砂土介质中Pu(Ⅳ)的分配系数(Kd)大于Pu(Ⅴ)的,并且分配系数随砂土介质中粘土矿物含量的增加及介质颗粒粒径减小而增大.%Pu exists in four different oxidation states( Ⅲ ,Ⅳ, Ⅴ , Ⅵ) with in the Eh( Redox Potential) and pH ranges of natural environment. Pu( Ⅳ) in Pu( OH)4 form and Pu( Ⅴ ) in PuO2(H2O)n+ form are the dominant oxidation states under equilibrium conditions for groundwater compositions. The sorption distribution coefficients (Kd) of Pu (Ⅳ ) and Pu ( Ⅴ) in the sand soil were studied by batch experiments, Kd of Pu (Ⅳ) is about 5. 5 × 103 mL/g to 4 × 104 mL/g, Kd of Pu( Ⅴ) is 3. 2 × 103 mL/g to 1. 1 × 104 mL/g. In conclusion, Kd values of Pu( Ⅳ) in the sand soil were larger than those of Pu( Ⅴ ). Such distribution coefficients increase with the increase of amount of clay in sand soil and the decrease of particle size.

  9. Prompt fission γ -ray spectrum characteristics from 240Pu(sf ) and 242Pu(sf )

    Science.gov (United States)

    Oberstedt, S.; Oberstedt, A.; Gatera, A.; Göök, A.; Hambsch, F.-J.; Moens, A.; Sibbens, G.; Vanleeuw, D.; Vidali, M.

    2016-05-01

    In this paper we present first results for prompt fission γ -ray spectra (PFGS) characteristics from the spontaneous fission (sf) of 240Pu and 242Pu. For 242Pu(sf ) we obtained, after proper unfolding of the detector response, an average energy per photon ɛ¯γ=(0.843 ±0.012 ) MeV, an average multiplicity M¯γ=(6.72 ±0.07 ) , and an average total γ -ray energy release per fission E¯γ ,tot = (5.66 ± 0.06) MeV. The 240Pu(sf ) emission spectrum was obtained by applying a so-called detector-response transformation function determined from the 242Pu spectrum measured in exactly the same geometry. The results are an average energy per photon ɛ¯γ=(0.80 ±0.07 ) MeV, the average multiplicity M¯γ = (8.2 ± 0.4), and an average total γ -ray energy release per fission E¯γ ,tot = (6.6 ± 0.5) MeV. The PFGS characteristics for 242Pu(sf ) are in very good agreement with those from thermal-neutron-induced fission on 241Pu and scales well with the corresponding prompt neutron multiplicity. Our results in the case of 240Pu(sf ), although drawn from a limited number of events, show a significantly enhanced average multiplicity and average total energy, but may be understood from a different fragment yield distribution in 240Pu(sf ) compared to that of 242Pu(sf ).

  10. Measurement of the 240Pu/239Pu mass ratio using a transition-edge-sensor microcalorimeter for total decay energy spectroscopy.

    Science.gov (United States)

    Hoover, Andrew S; Bond, Evelyn M; Croce, Mark P; Holesinger, Terry G; Kunde, Gerd J; Rabin, Michael W; Wolfsberg, Laura E; Bennett, Douglas A; Hays-Wehle, James P; Schmidt, Dan R; Swetz, Daniel; Ullom, Joel N

    2015-04-07

    We have developed a new category of sensor for measurement of the (240)Pu/(239)Pu mass ratio from aqueous solution samples with advantages over existing methods. Aqueous solution plutonium samples were evaporated and encapsulated inside of a gold foil absorber, and a superconducting transition-edge-sensor microcalorimeter detector was used to measure the total reaction energy (Q-value) of nuclear decays via heat generated when the energy is thermalized. Since all of the decay energy is contained in the absorber, we measure a single spectral peak for each isotope, resulting in a simple spectral analysis problem with minimal peak overlap. We found that mechanical kneading of the absorber dramatically improves spectral quality by reducing the size of radioactive inclusions within the absorber to scales below 50 nm such that decay products primarily interact with atoms of the host material. Due to the low noise performance of the microcalorimeter detector, energy resolution values of 1 keV fwhm (full width at half-maximum) at 5.5 MeV have been achieved, an order of magnitude improvement over α-spectroscopy with conventional silicon detectors. We measured the (240)Pu/(239)Pu mass ratio of two samples and confirmed the results by comparison to mass spectrometry values. These results have implications for future measurements of trace samples of nuclear material.

  11. Even–odd effects in prompt emission of spontaneously fissioning even–even Pu isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Tudora, A., E-mail: anabellatudora@hotmail.com [University of Bucharest, Faculty of Physics, Bucharest Magurele, POB MG-11, R-76900 (Romania); Hambsch, F.-J. [EC-JRC Institute for Reference Materials and Measurements (IRMM), Retieseweg 111, B-2440, Geel (Belgium); Giubega, G.; Visan, I. [University of Bucharest, Faculty of Physics, Bucharest Magurele, POB MG-11, R-76900 (Romania)

    2015-01-15

    The available experimental Y(A,TKE) data for {sup 236,238,240,242,244}Pu(SF) together with the Zp model prescription with appropriate parameters allows the investigation of even–odd effects in fragment distributions. The size of the global even–odd effect in Y(Z) is decreasing from {sup 244}Pu(SF) to {sup 236}Pu(SF) confirming the general observation of a decrease of the even–odd effect with the fissility parameter. Charge polarizations (ΔZ) and root-mean squares (rms) as a function of A of {sup 236–244}Pu(SF) were obtained for the first time. In the asymmetric fission region both ΔZ(A) and rms(A) exhibit oscillations with a periodicity of about 5 mass units due to the even–odd effects. The total average charge deviations 〈ΔZ〉 (obtained by averaging ΔZ(A) over the experimental Y(A) distribution) are of about |0.5| for all studied Pu(SF) systems. The comparison of the calculated ΔZ(A) and rms(A) of {sup 240}Pu(SF) with those of {sup 239}Pu(n{sub th},f) reported by Wahl shows an in-phase oscillation with a higher amplitude in the case of {sup 240}Pu(SF), confirming the higher even–odd effect in the case of SF. As in the previously studied cases ({sup 233,235}U(n{sub th},f), {sup 239}Pu(n{sub th},f), {sup 252}Cf(SF)) the even–odd effects in the prompt emission of {sup 236–244}Pu(SF) are mainly due to the Z even–odd effects in fragment distributions and charge polarizations and the N even–odd effects in the average neutron separation energies from fragments 〈Sn〉. The size of the global N even–odd effect in 〈Sn〉 is decreasing with the fissility parameter, being higher for the Pu(SF) systems compared to the previously studied systems. The prompt neutron multiplicities as a function of Z, ν(Z), exhibit sawtooth shapes with a visible staggering for asymmetric fragmentations. The size of the global Z even–odd effect in ν(Z) exhibits a decreasing trend with increasing fissility. The average prompt neutron multiplicities as a

  12. Heterogeneous reduction of {sup 239}PuO{sub 2} by aqueous Fe(II) in the presence of hematite

    Energy Technology Data Exchange (ETDEWEB)

    Felmy, A.R.; Moore, D.A.; Qafoku, O.; Buck, E.; Ilton, E.S. [Pacific Northwest National Laboratory, Richland, WA (United States); Conradson, S.D. [Los Alamos National Laboratory, NM (United States)

    2013-07-01

    The reduction of PuO{sub 2}(am) by Fe(II) in the presence and absence of hematite was studied over a range of pH values and oxidation/reduction potentials. In contrast to thermodynamic predictions, the presence of hematite did not have a major effect on the overall reduction of PuO{sub 2}(am) to aqueous Pu(III). Instead the aqueous Pu(III) concentrations at longer time frames were accurately predicted using the measured Fe(II) concentration and existing thermodynamic data for the reaction: H{sub 2}O + H{sup +} + Fe{sup 2+} + PuO{sub 2}(am) {r_reversible} Pu{sup 3+} + Fe(OH){sub 3}(am) with log K = -0.6. The accuracy of this approach in all solutions containing aqueous Fe(II), coupled with the apparent lack of oxidation of Fe(II) by O{sub 2}(g), suggests that the Fe(OH){sub 3}(am) is formed by the oxidation of Fe(II) to Fe(III) by radiolysis. The continued generation of reactive amorphous iron hydroxide by radiolysis prevents thermodynamic equilibrium from being reached with more stable ferric oxide compounds, except possibly under acidic conditions where amorphous ferric hydroxide is soluble. The use of measured pe values, instead of aqueous Fe(II) measurements, also yields reasonable predictions of the final Pu(III) concentrations although the predictions are more uncertain. (orig.)

  13. Knockdown of PU.1 AS lncRNA inhibits adipogenesis through enhancing PU.1 mRNA translation.

    Science.gov (United States)

    Pang, Wei-Jun; Lin, Li-Gen; Xiong, Yan; Wei, Ning; Wang, Yu; Shen, Qing-Wu; Yang, Gong-She

    2013-11-01

    PU.1 is an Ets family transcription factor involved in the myelo-lymphoid differentiation. We have previously demonstrated that PU.1 is also expressed in the adipocyte lineage. However, the expression levels of PU.1 mRNA and protein in preadipocytes do not match the levels in mature adipocytes. PU.1 mRNA level is higher in preadipocytes, whereas its protein is expressed in the adipocytes but not in the preadipocytes. The underlying mechanism remains elusive. Here, we find that miR-155 knockdown or overexpression has no effect on the levels of PU.1 mRNA and protein in preadipocytes or adipocytes. MiR-155 regulates adipogenesis not through PU.1, but via C/EBPβ which is another target of miR-155. We also checked the expression levels of PU.1 mRNA and antisense long non-coding RNA (AS lncRNA). Interestingly, compared with the level of PU.1 mRNA, the level of PU.1 AS lncRNA is much higher in preadipocytes, whereas it is opposite in the adipocytes. We further discover that PU.1 AS lncRNA binds to its mRNA forming an mRNA/AS lncRNA compound. The knockdown of PU.1 AS by siRNA inhibits adipogenesis and promotes PU.1 protein expression in both preadipocytes and adipocytes. Furthermore, the repression of PU.1 AS decreases the expression and secretion of adiponectin. We also find that the effect of retroviral-mediated PU.1 AS knockdown on adipogenesis is consistent with that of PU.1 AS knockdown by siRNA. Taken together, our results suggest that PU.1 AS lncRNA promotes adipogenesis through preventing PU.1 mRNA translation via binding to PU.1 mRNA to form mRNA/AS lncRNA duplex in preadipocytes.

  14. Concordant 241Pu-241Am Dating of Environmental Samples: Results from Forest Fire Ash

    Science.gov (United States)

    Goldstein, S. J.; Oldham, W. J.; Murrell, M. T.; Katzman, D.

    2010-12-01

    We have measured the Pu, 237Np, 241Am, and 151Sm isotopic systematics for a set of forest fire ash samples from various locations in the western U.S. including Montana, Wyoming, Idaho, and New Mexico. The goal of this study is to develop a concordant 241Pu (t1/2 = 14.4 y)-241Am dating method for environmental collections. Environmental samples often contain mixtures of components including global fallout. There are a number of approaches for subtracting the global fallout component for such samples. One approach is to use 242Pu/239Pu as a normalizing isotope ratio in a three-isotope plot, where this ratio for the non-global fallout component can be estimated or assumed to be small. This study investigates a new, complementary method of normalization using the long-lived fission product, 151Sm (t1/2 = 90 y). We find that forest fire ash concentrates actinides and fission products with ~1E10 atoms 239Pu/g and ~1E8 atoms 151Sm/g, allowing us to measure these nuclides by mass spectrometric (MIC-TIMS) and radiometric (liquid scintillation counting) methods. The forest fire ash samples are characterized by a western U.S. regional isotopic signature representing varying mixtures of global fallout with a local component from atmospheric testing of nuclear weapons at the Nevada Test Site (NTS). Our results also show that 151Sm is well correlated with the Pu nuclides in the forest fire ash, suggesting that these nuclides have similar geochemical behavior in the environment. Results of this correlation indicate that the 151Sm/239Pu atom ratio for global fallout is ~0.164, in agreement with an independent estimate of 0.165 based on 137Cs fission yields for atmospheric weapons tests at the NTS. 241Pu-241Am dating of the non-global fallout component in the forest fire ash samples yield ages in the late 1950’s-early 1960’s, consistent with a peak in NTS weapons testing at that time. The age results for this component are in agreement using both 242Pu and 151Sm normalizations

  15. Oxidation behaviour of plutonium rich (U, Pu)C and (U, Pu)O2

    Science.gov (United States)

    Sali, S. K.; Kulkarni, N. K.; Phatak, Rohan; Agarwal, Renu

    2016-10-01

    Oxidation behaviour of (U0.3Pu0.7)C1.06 was investigated in air by heating samples up to 1073 K and 1273 K. Thermogravimetry (TG) of the samples and X-ray powder diffraction (XRD) of the intermediate products were used to understand the phenomenon taking place during this process. Theoretical calculations were carried out to understand the multiple phase changes taking place during oxidation of carbide. Theoretical results were validated by XRD analysis of the products obtained at different stages of oxidation. The final oxidized products were found to be a single FCC phase with O/M = 2.15 (M = U + Pu). Oxidation kinetic studies of (U0.3Pu0.7)O2 and (U0.47Pu0.53)O2 were carried out in dry air, using thermogravimetry, under non-isothermal conditions. The activation energy of oxidation was found to be 49 and 70 kJ/mol, respectively. Lattice parameter dependence on Pu/M and O/M of plutonium rich mixed oxide (MOX) was established using combined results of XRD and TG analysis of (U0.3Pu0.7)O2+x and (U0.47Pu0.53)O2+x.

  16. Effect of polyurethane (PU) - bioactive glass (BG) ratio on the development of BG reinforced PU scaffold

    Science.gov (United States)

    Lip, Lim Weng; Abdullah, Tuti Katrina; Zubir, Syazana Ahmad

    2016-12-01

    Nowadays, variety of biomaterials may be used to produce implanted scaffolds such as metal-based, ceramic-based and polymer-based materials. In this study, porous bioactive glass (BG) reinforced polyurethane (PU) composite scaffolds with different PU:BG mass ratio (10 to 40 wt%) were fabricated as a potential candidate for synthetic bone graft. The PU-BG scaffolds were prepared using solvent casting combined with salt leaching (SCPL) method and were subjected to several characterizations including fourier transform infra-red (FTIR) spectroscopy, scanning electron microscopy (SEM) and energy dispersive x-ray spectroscopy (EDX). FTIR spectrum showed the trace of BG particles in the PU-BG scaffolds with high concentration of BG (30 and 40 wt%). EDX confirmed that the white particles in the PU-BG scaffold as observed via SEM micrograph were BG particles. A slightly round and irregular pore structures were observed for the PU-BG scaffolds prepared in this study. More homogeneous pore structures were observed as the amount of BG in the PU-BG scaffold is increased. The overall pore size for all scaffolds was in the range of 130 to 400 µm which is suitable for the growth of bone tissue.

  17. Presence of plutonium isotopes, {sup 239}Pu and {sup 240}Pu, in soils from Chile

    Energy Technology Data Exchange (ETDEWEB)

    Chamizo, E., E-mail: echamizo@us.es [Centro Nacional de Aceleradores, Avda. Thomas Alba Edison, 7, 41092 Sevilla (Spain); Garcia-Leon, M., E-mail: manugar@us.es [Departamento de Fisica Atomica, Molecular y Nuclear, Universidad de Sevilla, Avda. Reina Mercedes sn, 41012 Seville (Spain); Peruchena, J.I., E-mail: jiperuchena@gmail.com [Centro Nacional de Aceleradores, Avda. Thomas Alba Edison, 7, 41092 Sevilla (Spain); Cereceda, F., E-mail: francisco.cereceda@usm.cl [Laboratorio de Quimica Ambiental, Centro de Tecnologias Ambientales (CETAM), Universidad Tecnica Federico Santa Maria, Casilla 110-V, Valparaiso (Chile); Vidal, V., E-mail: victor.vidal@usm.cl [Laboratorio de Quimica Ambiental, Centro de Tecnologias Ambientales (CETAM), Universidad Tecnica Federico Santa Maria, Casilla 110-V, Valparaiso (Chile); Pinilla, E., E-mail: epinilla@unex.es [Departamento de Quimica Analitica, Facultad de Ciencias, Universidad de Extremadura, Avda. de Elvas sn, 06071 Badajoz (Spain); Miro, C., E-mail: cmiro@unex.es [Departamento de Fisica Aplicada, Universidad de Extremadura, Avda. de la Universidad sn, 10071 Caceres (Spain)

    2011-12-15

    Plutonium is present in every environmental compartment, due to a variety of nuclear activities. The Southern Hemisphere has received about 20% of the global {sup 239}Pu and {sup 240}Pu environmental inventory, with an important contribution of the so-called tropospheric fallout from both the atmospheric nuclear tests performed in the French Polynesia and in Australia by France and United Kingdom, respectively. In this work we provide new data on the impact of these tests to South America through the study of {sup 239}Pu and {sup 240}Pu in soils from different areas of Northern, Central and Southern Chile. The obtained results point out to the presence of debris from the French tests in the 20-40 Degree-Sign Southern latitude range, with {sup 240}Pu/{sup 239}Pu atomic ratios quite heterogeneous and ranging from 0.02 to 0.23. They are significantly different from the expected one for the global fallout in the Southern Hemisphere for the 30-53 Degree-Sign S latitude range (0.185 {+-} 0.047), but they follow the same trend as the reported values by the Department of Energy of United States for other points with similar latitudes. The {sup 239+240}Pu activity inventories show as well a wider variability range in that latitude range, in agreement with the expected heterogeneity of the contamination.

  18. Neutron Capture Cross Section of 239Pu

    Science.gov (United States)

    Mosby, S.; Arnold, C.; Bredeweg, T. A.; Couture, A.; Jandel, M.; O'Donnell, J. M.; Rusev, G.; Ullmann, J. L.; Chyzh, A.; Henderson, R.; Kwan, E.; Wu, C. Y.

    2014-09-01

    The 239Pu(n,γ) cross section has been measured over the energy range 10 eV - 10 keV using the Detector for Advanced Neutron Capture Experiments (DANCE) as part of a campaign to produce precision (n,γ) measurements on 239Pu in the keV region. Fission coincidences were measured with a PPAC and used to characterize the prompt fission γ-ray spectrum in this region. The resulting spectra will be used to better characterize the fission component of another experiment with a thicker target to extend the (n,γ) cross section measurement well into the keV region.

  19. Isotopic characterization and thermal neutron flux determination of a PuBe neutron source.

    Science.gov (United States)

    Purty, Ravi Ankit; Akanchha; Prasad, Shikha

    2017-07-01

    The Indian Institute of Technology Kanpur (IIT Kanpur) possesses a PuBe neutron source facility with an initial activity of 5 Ci, dated September 1966 (nearly 50 years ago). An understanding of the present activity and the rate of its change will allow implementation of proper radiological safety procedures and future radiological safety planning. Knowing the absolute neutron flux will help us in future neutron activation studies. These details are also important to ensure proper security precautions. In our work, we attempt to identify the isotopic composition to determine the rate of change of the source and the absolute thermal neutron flux of plutonium beryllium (PuBe) sample at IIT Kanpur. We have used gamma-ray spectroscopy for determining the isotopic composition of the PuBe neutron source. After utilizing gamma-ray spectroscopy it is found that the source is composed of (239)Pu and a small amount of (241)Am is present as an impurity. The mass ratio of (241)Am to (239)Pu is found to be approximately 18.1µg/g with an uncertainty of 1.39%. Delayed gamma neutron activation analysis (DGNAA) is used to determine the thermal neutron flux of the same PuBe neutron source using copper, cobalt, nickel and cadmium samples. The average thermal neutron flux as calculated from DGNAA is approximately 1.27×10(3)n/(cm(2)-s) at 1cm above the PuBe neutron source. Copyright © 2017 Elsevier Ltd. All rights reserved.

  20. Stabilization of Rocky Flats Pu-contaminated ash within chemically bonded phosphate ceramics

    Science.gov (United States)

    Wagh, A. S.; Strain, R.; Jeong, S. Y.; Reed, D.; Krause, T.; Singh, D.

    A feasibility study was conducted on the use of chemically bonded phosphate ceramics for stabilization of combustion residue of high transuranic (TRU) wastes. Using a matrix of magnesium potassium phosphate formed by the room-temperature reaction of MgO and KH 2PO 4 solution, we made waste forms that contained 5 wt% Pu to satisfy the requirements of the Waste Isolation Pilot Plant. The waste forms were ceramics whose compression strength was twice that of conventional cement grout and whose connected porosity was ≈50% that of cement grout. Both surrogate and actual waste forms displayed high leaching resistance for both hazardous metals and Pu. Hydrogen generation resulting from the radiolytic decomposition of water and organic compounds present in the waste form did not appear to be a significant issue. Pu was present as PuO 2 that was physically microencapsulated in the matrix. In the process, pyrophoricity was removed and leaching resistance was enhanced. The high leaching resistance was due to the very low solubility of PuO 2 coupled with superior microencapsulation. As a result, the waste forms satisfied the current Safeguard Termination Limit requirement for storage of TRU combustion residues.

  1. Designing of Multiphase Fly Ash/MWCNT/PU Composite Sheet Against Electromagnetic Environmental Pollution

    Science.gov (United States)

    Gujral, Parth; Varshney, Swati; Dhawan, S. K.

    2016-06-01

    Fly ash and multiwalled carbon nanotubes (MWCNT) reinforced multiphase polyurethane (PU) composite sheets have been fabricated by using a solution casting technique. Utilization of fly ash was the prime objective in order to reduce environmental pollution and to enhance the shielding properties of PU polymer. Our study proves that fly ash particles with MWCNTs in a PU matrix leads to novel hybrid high performance electromagnetic shielding interference material. Scanning electron microscopy confirms the existence of fly ash particles along with MWCNTs in a PU matrix. This multiphase composite shows total shielding effectiveness of 35.8 dB (>99.99% attenuation) in the Ku-band (12.4-18 GHz) frequency range. This is attributed to high dielectric losses of reinforcement present in the polymers matrix. The Nicolson-Ross-Weir algorithm has been applied to calculate the electromagnetic attributes and dielectric parameters of the PU samples by using scattering parameters ( S 11, S 22, S 12, S 21). The synthesized multiphase composites were further characterized by using x-ray diffraction, Fourier transform infrared spectroscopy, and thermo gravimetric analysis.

  2. Genetic mapping, marker assisted selection and allelic relationships for the Pu 6 gene conferring rust resistance in sunflower.

    Science.gov (United States)

    Bulos, Mariano; Vergani, Pablo Nicolas; Altieri, Emiliano

    2014-09-01

    Rust resistance in the sunflower line P386 is controlled by Pu 6 , a gene which was reported to segregate independently from other rust resistant genes, such as R 4 . The objectives of this work were to map Pu 6 , to provide and validate molecular tools for its identification, and to determine the linkage relationship of Pu 6 and R 4 . Genetic mapping of Pu 6 with six markers covered 24.8 cM of genetic distance on the lower end of linkage Group 13 of the sunflower consensus map. The marker most closely linked to Pu 6 was ORS316 at 2.5 cM in the distal position. ORS316 presented five alleles when was assayed with a representative set of resistant and susceptible lines. Allelism test between Pu 6 and R 4 indicated that both genes are linked at a genetic distance of 6.25 cM. This is the first confirmation based on an allelism test that at least two members of the R adv /R 4 /R 11 / R 13a /R 13b /Pu 6 cluster of genes are at different loci. A fine elucidation of the architecture of this complex locus will allow designing and constructing completely new genomic regions combining genes from different resistant sources and the elimination of the linkage drag around each resistant gene.

  3. DFT and two-dimensional correlation analysis methods for evaluating the Pu{sup 3+}–Pu{sup 4+} electronic transition of plutonium-doped zircon

    Energy Technology Data Exchange (ETDEWEB)

    Bian, Liang, E-mail: bianliang@ms.xjb.ac.cn [Key Laboratory of Functional Materials and Devices for Special Environments, Chinese Academy of Sciences, Urumqi 830011, Xinjiang (China); Laboratory for Extreme Conditions Matter Properties, South West University of Science and Technology, Mianyang 621010, Sichuan (China); Dong, Fa-qin; Song, Mian-xin [Laboratory for Extreme Conditions Matter Properties, South West University of Science and Technology, Mianyang 621010, Sichuan (China); Dong, Hai-liang [Department of Geology and Environmental Earth Science, Miami University, Oxford, OH 45056 (United States); Li, Wei-Min [Key Laboratory of Functional Materials and Devices for Special Environments, Chinese Academy of Sciences, Urumqi 830011, Xinjiang (China); Duan, Tao; Xu, Jin-bao [Laboratory for Extreme Conditions Matter Properties, South West University of Science and Technology, Mianyang 621010, Sichuan (China); Zhang, Xiao-yan [Key Laboratory of Functional Materials and Devices for Special Environments, Chinese Academy of Sciences, Urumqi 830011, Xinjiang (China); Laboratory for Extreme Conditions Matter Properties, South West University of Science and Technology, Mianyang 621010, Sichuan (China)

    2015-08-30

    Highlights: • Effect of Pu f-shell electron on the electronic property of zircon is calculated via DFT and 2D-CA techniques. • Reasons of Pu f-shell electron influencing on electronic properties are systematically discussed. • Phase transitions are found at two point 2.8 mol% and 7.5 mol%. - Abstract: Understanding how plutonium (Pu) doping affects the crystalline zircon structure is very important for risk management. However, so far, there have been only a very limited number of reports of the quantitative simulation of the effects of the Pu charge and concentration on the phase transition. In this study, we used density functional theory (DFT), virtual crystal approximation (VCA), and two-dimensional correlation analysis (2D-CA) techniques to calculate the origins of the structural and electronic transitions of Zr{sub 1−c}Pu{sub c}SiO{sub 4} over a wide range of Pu doping concentrations (c = 0–10 mol%). The calculations indicated that the low-angular-momentum Pu-f{sub xy}-shell electron excites an inner-shell O-2s{sup 2} orbital to create an oxygen defect (V{sub O-s}) below c = 2.8 mol%. This oxygen defect then captures a low-angular-momentum Zr-5p{sup 6}5s{sup 2} electron to form an sp hybrid orbital, which exhibits a stable phase structure. When c > 2.8 mol%, each accumulated V{sub O-p} defect captures a high-angular-momentum Zr-4d{sub z} electron and two Si-p{sub z} electrons to create delocalized Si{sup 4+} → Si{sup 2+} charge disproportionation. Therefore, we suggest that the optimal amount of Pu cannot exceed 7.5 mol% because of the formation of a mixture of ZrO{sub 8} polyhedral and SiO{sub 4} tetrahedral phases with the orientation (10-1). This study offers new perspective on the development of highly stable zircon-based solid solution materials.

  4. Rapid Separation of 239Pu and 241Am in Environment Soil Samples

    Institute of Scientific and Technical Information of China (English)

    YANG; Jin-ling; ZHANG; Ji-qiao; HUANG; Kun; DING; You-qian; ZHAO; Ya-ping

    2015-01-01

    In the nuclear sites and the surroundings which are the main environmental monitored area,the allowances of 239Pu and 241 Am are less than0.1Bq/g as the extremely toxic species.So it is very important and practical to establish rapid and convenient analysis methods for them.With

  5. PuFT: Computer-Assisted Program for Pulmonary Function Tests.

    Science.gov (United States)

    Boyle, Joseph

    1983-01-01

    PuFT computer program (Microsoft Basic) is designed to help in understanding/interpreting pulmonary function tests (PFT). The program provides predicted values for common PFT after entry of patient data, calculates/plots graph simulating force vital capacity (FVC), and allows observations of effects on predicted PFT values and FVC curve when…

  6. Preparation of Pu Target with Small Area

    Institute of Scientific and Technical Information of China (English)

    SUN; Xiao-yi; MAO; Guo-shu; HUANG; Kun; YANG; Lei; YANG; Su-liang; YANG; Chun-li; SUN; Hong-qing; MA; Peng

    2015-01-01

    Plutonium can be electrodeposited in ammonium oxalate,ammonium sulfate and ammonium chloride systems,but there is white layer appeared when the diameter of the active area is7mm and Pu is electrodeposited in isopropanol,and large amount of hydrogen is generated near the cathode in ammonium sulfate,which covers

  7. Superdeformed Rotational Bands in 240Pu

    Science.gov (United States)

    Hunyadi, M.; Gassmann, D.; Krasznahorkay, A.; Habs, D.; Csatlos, M.; Eisermann, Y.; Faestermann, T.; Graw, G.; Gulyas, J.; Hertenberger, R.; Maier, H. J.; Mate, Z.; Metz, A.; Thirolf, P.; Chromik, M.; van der Werf, S. Y.

    2001-03-01

    The intermediate structure of the fission resonances has been observed in 240Pu. A resonance structure found around the excitation energy of 4.5 MeV was interpreted as a group of Kπ =0+ superdeformed rotational bands. The moments of inertia and level density distributions were also deduced for the individually observed band-heads.

  8. Superdeformed rotational bands in Pu-240

    NARCIS (Netherlands)

    Hunyadi, M; Gassmann, D; Krasznahorkay, A; Habs, D; Csatlos, M; Eisermann, Y; Faestermann, T; Graw, G; Gulyas, J; Hertenberger, R; Maier, HJ; Mate, Z; Metz, A; Thirolf, P; Chromik, M; van der Werf, SY

    The intermediate structure of the fission resonances has been observed in Pu-240. A resonance structure found around the excitation energy of 4.5 MeV was interpreted as a group of K-pi = 0(+) superdeformed rotational bands. The moments of inertia and level density distributions were also deduced for

  9. Anomalous atomic volume of alpha-Pu

    DEFF Research Database (Denmark)

    Kollar, J.; Vitos, Levente; Skriver, Hans Lomholt

    1997-01-01

    .3%. The comparison between the LDA and GGA results show that the anomalously large atomic volume of alpha-Pu relative to alpha-Np can be ascribed to exchange-correlation effects connected with the presence of low coordinated sites in the structure where the f electrons are close to the onset of localization...

  10. Entretien avec Aleksandr A. Puškin & Maria A. Puškinova

    Directory of Open Access Journals (Sweden)

    Katia Vandenborre

    2010-06-01

    Full Text Available PrésentationAleksandr Puškin, le « soleil de la poésie russe », n’a jamais mis pied dans nos régions, mais c’est bien en Belgique que vivent ses deux descendants les plus directs : Aleksandr Aleksandrovič Puškin et son épouse Maria Aleksandrovna, lesquels s’efforcent de mieux faire connaître le nom de Puškin, notamment par le biais de la Fondation Internationale A. S. Pouchkine. Les époux Puškin ont eu la gentillesse de nous accueillir dans leur appartement bruxellois et de nous guider à trav...

  11. Investigation of zircon/zirconia ceramics doped with {sup 239}Pu and {sup 238}Pu

    Energy Technology Data Exchange (ETDEWEB)

    Burakov, B.E.; Anderson, E.B.; Zamoryanskaya, M.V.; Nikolaeva, E.V.; Strykanova, E.E.; Yagovkina, M.A. [V.G. Khlopin Radium Institute, Saint Petersburg (Russian Federation)

    2001-07-01

    Several samples of crystalline double-phase ceramics based on zircon, (Zr,Pu)SiO{sub 4} and zirconia, (Zr,Pu)O{sub 2}, were synthesized by sintering in air, precursors containing approximately 5-6 and 10 wt% {sup 239}Pu, respectively. One sample doped with 5-6 wt% {sup 238-39-40}Pu was also obtained under the same conditions. All ceramic samples were studied by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), electron probe microanalysis (EPMA) and MCC-1 leach test in deionized water at 90 C. Results indicate that even radiation damaged zircon/zirconia ceramics retain high chemical resistance and mechanical durability. (author)

  12. The 239 Pu(n,2n)238Pu cross section: preliminary calculations

    Energy Technology Data Exchange (ETDEWEB)

    Chen, H; Reffo, G; Ross, M A; White, R M

    1999-03-12

    The primary motivation for the present work is to provide theoretical values for the ratio of the partial 239Pu(n,2nx{gamma})238Pu to total 239 Pu(n,2n)238Pu cross section for several discrete gamma transitions. Results and conclusions of preliminary calculations from threshold to 20 MeV are presented. Calculations are based on theoretical models with parameters obtained from the literature or from our ad hoc systematics. Optical model cross sections and transmission coefficients were determined using the coupled-channels method. The calculations included a preequilibrium component followed by multiple particle and gamma-ray emissions. Fission competition was included at all stages of de-excitation. Suggestions for further verifications and possible improvements are provided.

  13. Statistical properties of 243Pu, and 242Pu(n ,γ ) cross section calculation

    Science.gov (United States)

    Laplace, T. A.; Zeiser, F.; Guttormsen, M.; Larsen, A. C.; Bleuel, D. L.; Bernstein, L. A.; Goldblum, B. L.; Siem, S.; Garotte, F. L. Bello; Brown, J. A.; Campo, L. Crespo; Eriksen, T. K.; Giacoppo, F.; Görgen, A.; Hadyńska-KlÈ©k, K.; Henderson, R. A.; Klintefjord, M.; Lebois, M.; Renstrøm, T.; Rose, S. J.; Sahin, E.; Tornyi, T. G.; Tveten, G. M.; Voinov, A.; Wiedeking, M.; Wilson, J. N.; Younes, W.

    2016-01-01

    The level density and γ -ray strength function (γ SF ) of 243Pu have been measured in the quasicontinuum using the Oslo method. Excited states in 243Pu were populated using the 242Pu(d ,p ) reaction. The level density closely follows the constant-temperature level density formula for excitation energies above the pairing gap. The γ SF displays a double-humped resonance at low energy as also seen in previous investigations of actinide isotopes. The structure is interpreted as the scissors resonance and has a centroid of ωSR=2.42 (5 ) MeV and a total strength of BSR=10.1 (15 ) μN2 , which is in excellent agreement with sum-rule estimates. The measured level density and γ SF were used to calculate the 242Pu(n ,γ ) cross section in a neutron energy range for which there were previously no measured data.

  14. Electronic structure of delta-Pu and PuCoGa[sub 3] from photoemission and the mixed level model

    Energy Technology Data Exchange (ETDEWEB)

    Joyce, J. J. (John Joseph); Wills, J. M. (John M.); Durakiewicz, T. (Tomasz); Butterfield, M. T. (Martin T.); Guziewicz, E. (Elzbieta); Sarrao, John L.,; Arko, A. J. (Aloysius J.); Moore, D. P. (David P.); Morales, L. A. (Luis A.); Eriksson, O. (Olle)

    2004-01-01

    The electronic structure of {delta}-phase Pu metal and the Pu-based superconductor PuCoGa{sub 5} is explored using photoelectron spectroscopy and a novel theoretical scheme. Excellent agreement between calculation and experiment defines a path forward for understanding electronic structure aspects of Pu-based materials. The photoemission results show two separate regions of 5f electron spectral intensity, one at the Fermi energy and another centered 1.2 eV below the Fermi level. A comparison is made between the photoemission data and five computational schemes for {delta}-Pu. The results for {delta}-Pu and PuCoGa{sub 5} indicate 5f electron behavior on the threshold between localized and itinerant and a broader framework for understanding the fundamental electronic properties of the Pu 5f levels in general within two configurations, one localized and one itinerant.

  15. Vertical distributions of radionuclides ((239+240)Pu, (240)Pu/(239)Pu, and (137)Cs) in sediment cores of Lake Bosten in Northwestern China.

    Science.gov (United States)

    Liao, Haiqing; Bu, Wenting; Zheng, Jian; Wu, Fengchang; Yamada, Masatoshi

    2014-04-01

    Artificial radionuclides ((137)Cs, (239+240)Pu, (241)Pu, (241)Am) deposited in lacustrine sediments have been used for dating as well as radionuclide source identification. In the present work, we investigated the vertical distributions of (239+240)Pu and (137)Cs activities, (240)Pu/(239)Pu atom ratios, and (239+240)Pu/(137)Cs activity ratios in sediment cores collected from Lake Bosten, which is the lake closest to the Lop Nor Chinese Nuclear Weapon Test site in northwestern China. Uniformly high concentrations of (239+240)Pu and (137)Cs were found in the upper layers deposited since 1964 in the sediment cores, and these were controlled by the resuspension of soil containing radionuclides from the nearby land surface. As the Chinese nuclear tests varied remarkably in yield, the mixing of the tropospheric deposition from these tests and the stratospheric deposition of global fallout has led to a (240)Pu/(239)Pu atom ratio that is similar to that of global fallout and to a (239+240)Pu/(137)Cs activity ratio that is slightly higher than that of global fallout. However, a low (240)Pu/(239)Pu atom ratio of 0.080 and high (239+240)Pu/(137)Cs activity ratio of 0.087, significantly different from the global fallout values, were observed in one sediment core (07BS10-2), indicating the inhomogenous tropospheric deposition from the Chinese nuclear tests in Lake Bosten during 1967-1973. These results are important to understand the influence of the CNTs on the radionuclide contamination in Lake Bosten.

  16. Determination of Pu in soil samples; Determinacion de Pu en muestras de suelo

    Energy Technology Data Exchange (ETDEWEB)

    Torres C, C. O.; Hernandez M, H.; Romero G, E. T. [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico); Vega C, H. R., E-mail: carioli_32907@hotmail.com [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Cipres No. 10, Fracc. La Penuela, 98068 Zacatecas, Zac. (Mexico)

    2016-10-15

    The irreversible consequences of accidents occurring in nuclear plants and in nuclear fuel reprocessing sites are mainly the distribution of different radionuclides in different matrices such as the soil. The distribution in the superficial soil is related to the internal and external exposure to the radiation of the affected population. The internal contamination with radionuclides such as Pu is of great relevance to the nuclear forensic science, where is important to know the chemical and isotopic compositions of nuclear materials. The objective of this work is to optimize the radiochemical separation of plutonium (Pu) from soil samples and to determine their concentration. The soil samples were prepared using acid digestion assisted by microwave; purification of Pu was carried out with AG1X8 resin using ion exchange chromatography. Pu isotopes were measured using ICP-SFMS. In order to reduce the interference due to the presence of {sup 238}UH {sup +} in the samples, a solvent removal system (Apex) was used. In addition, the limit of detection and quantification of Pu was determined. It was found that the recovery efficiency of Pu in soil samples ranges from 70 to 93%. (Author)

  17. Analysis Method of 241Pu Radioactivity by Isotope Dilution-Extraction Liquid Scintillation Spectrometer

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    <正>241Pu is the only pure β emitter with the maximum energy of 20.81 keV in plutonium isotopes of 238Pu, 239Pu, 240Pu and 242Pu, in which 241Pu is mostly specific radioactivity because its half-life is 14.29 a.

  18. Pu speciation in actual and simulated aged wastes

    Energy Technology Data Exchange (ETDEWEB)

    Lezama-pacheco, Juan S [Los Alamos National Laboratory; Conradson, Steven D [Los Alamos National Laboratory

    2008-01-01

    X-ray Absorption Fine Structure Spectroscopy (XAFS) at the Pu L{sub II/III} edge was used to determine the speciation of this element in (1) Hanford Z-9 Pu crib samples, (2) deteriorated waste resins from a chloride process ion-exchange purification line, and (3) the sediments from two Waste Isolation Pilot Plant Liter Scale simulant brine systems. The Pu speciation in all of these samples except one is within the range previously displayed by PuO{sub 2+x-2y}(OH){sub y}{center_dot}zH{sub 2}O compounds, which is expected based on the putative thermodynamic stability of this system for Pu equilibrated with excess H{sub 2}O and O{sub 2} under environmental conditions. The primary exception was a near neutral brine experiment that displayed evidence for partial substitution of the normal O-based ligands with Cl{sup -} and a concomitant expansion of the Pu-Pu distance relative to the much more highly ordered Pu near neighbor shell in PuO{sub 2}. However, although the Pu speciation was not necessarily unusual, the Pu chemistry identified via the history of these samples did exhibit unexpected patterns, the most significant of which may be that the presence of the Pu(V)-oxo species may decrease rather than increase the overall solubility of these compounds. Several additional aspects of the Pu speciation have also not been previously observed in laboratory-based samples. The molecular environmental chemistry of Pu is therefore likely to be more complicated than would be predicted based solely on the behavior of PuO{sub 2} under laboratory conditions.

  19. Preliminary studies of Pu measurement by AMS using PuF{sub 4}{sup -}

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, X.-L., E-mail: xzha5@uottawa.ca [Department of Physics, University of Ottawa, 150 Louis Pasteur, Ottawa, ON., K1N 6N5 (Canada); Kieser, W.E. [Department of Physics, University of Ottawa, 150 Louis Pasteur, Ottawa, ON., K1N 6N5 (Canada); Dai, X.; Priest, N.D.; Kramer-Tremblay, S. [Chalk River Laboratories, AECL, Chalk River, ON., K0J 1J0 (Canada); Eliades, J.; Litherland, A.E. [IsoTrace Laboratory, University of Toronto, 60 St. George St., Toronto, ON., M5S 1A7 (Canada)

    2013-01-15

    Using targets made with PbF{sub 2} matrices, Cs{sup +} sputter sources have been found to yield element-specific patterns of molecular fluoride anions that may be used to enhance the mass spectrometry of certain elements. While the patterns are found similar for all lanthanides and the heavier actinides, substantial differences are found for the lighter actinides. In the case of Pu and U, of all their fluoride anions, PuF{sub 4}{sup -} and UF{sub 5}{sup -} are produced with the highest yield. Mass spectrometry of Pu using PuF{sub 4}{sup -} can provide a partial chemical separation in the ion source, as the yield of UF{sub 4}{sup -} is two orders of magnitude lower than that of the UF{sub 5}{sup -}. This, in turn, reduces scattering of U ions when measuring Pu in the high-energy components of the AMS system. This instrumental reduction of U is advantageous in cases that require rapid Pu analyses as it simplifies the chemistry of Pu/U separation and other steps in the sample processing. In this procedure, Pu can be co-precipitated with another element as a fluoride, which is then mixed with a sufficient amount of PbF{sub 2} powder to form a sputter target. A series of tests were carried out and NdF{sub 3} was identified as one such suitable carrier. Measurements of Pu{sup +3} at {approx}0.85 MV terminal voltage showed that the {sup 239,240,241,242}Pu isotopes can be detected with a manageably low background, high efficiency and a 1 fg detection limit. Preliminary tests were carried out using the existing IsoTrace AMS system, modified only by the addition of electronic controls to automatically adjust the terminal voltage and all high-energy electric analyzers, along with the injection magnet bouncer. However, both the injection and detection systems were not designed for this task, so considerable room is available for reducing the detection limit into the ag range with modern AMS systems - such as the one being commissioned at University of Ottawa.

  20. Application of laser-induced photoacoustic spectroscopy for determination of plutonium concentration in nuclear waste solutions.

    Science.gov (United States)

    Surugaya, Naoki; Sato, Soichi; Jitsukata, Syu; Watahiki, Masaru

    2008-04-01

    Laser-induced photoacoustic spectroscopy was used in a quantitative analysis of Pu in HNO3 medium. Plutonium was quantitatively oxidized to Pu(VI) using Ce(IV). The photoacoustic measurement of Pu(VI) with maximum absorption at 830.5 nm was subsequently performed to determine the concentration. The photoacoustic signal was linearly proportional to the Pu(VI) ion concentration. The detection limit of Pu(VI) was estimated to be 0.5 microg mL(-1) (3sigma) in 3 M HNO3. By the proposed method, Pu concentration was successfully determined in a nuclear waste solution for use in nuclear materials management.

  1. Pu and Am determination in the environment—method development

    Science.gov (United States)

    Afonin, M.; Simonoff, M.; Donard, O.; Michel, H.; Ardisson, G.

    2003-01-01

    A high resolution inductively coupled plasma mass spectrometric (HR-ICP-MS) method for the determination of plutonium isotopes, Am and the 240Pu/239Pu isotope ratio utilising modification of Pu-02-RC Plutonium in Soil Samples, Pu-03-RC Plutonium in Soil Residue—Total Dissolution Method, Pu-11-RC Plutonium Purification—Ion Exchange Technique, Pu-12-RC Plutonium and/or Americium in Soil or Sediments, HASL-300 was developed. Total plutonium concentrations (239+240Pu) measured in environmental samples by this HR-ICP-MS method were in good agreement with recommended data obtained from a-spectrometry. It was achieved the decreasing of the time to analyze the samples over than 33%.

  2. Solid Solubilities of Pu, U, Gd and Hf in Candidate Ceramic Nuclear Wasteforms

    Energy Technology Data Exchange (ETDEWEB)

    Vance, Eric R.; Carter, M. L.; Lumpkin, G. R.; Day, R. A.; Begg, B. D.

    2001-04-02

    This goal of this research project was to determine the solid solubility of Pu, U, Gd, and Hf in candidate ceramics for immobilization of high-level nuclear waste. The experimental approach was to saturate each phase by adding more than the solid solubility limit of the given cation, using a nominated substitution scheme, and then analyzing the candidate phase that formed to evaluate the solid solubility limit under firing conditions. Confirmation that the solid solution limit had been reached insofar as other phases rich in the cation of interest was also required. The candidate phases were monazite, titanite, zirconolite, perovskite, apatite, pyrochlore, and brannerite. The valences of Pu and U were typically deduced from the firing atmosphere, and charge balancing in the candidate phase composition as evaluated from electron microscopy, although in some cases it was measured directly by x-ray absorption and diffuse reflectance spectroscopies (for U). Tetravalent Pu and U have restricted (< 0.1 formula units) solid solubility in apatite, titanite, and perovskite. Trivalent Pu has a larger solubility in apatite and perovskite than Pu4+. U3+ appears to be a credible species in reduced perovskite with a solubility of {approximately} 0.25 f.u. as opposed to {approximately} 0.05 f.u. for U4+. Pu4+ is a viable species in monazite and is promoted at lower firing temperatures ({approximately} 800 C) in an air atmosphere. Hf solubility is restricted in apatite, monazite (< 0.1 f.u.), but is {approximately} 0.2 and 0.5 f.u. in brannerite and titanite, respectively. Gd solubility is extended in all phases except for titanite ({approximately} 0.3 f.u.). U5+ was identified by DRS observations of absorption bands in the visible/near infrared photon energy ranges in brannerite and zirconolite, and U4+ in zirconolite was similarly identified.

  3. Solid Solubilities of Pu, U, Gd and Hf in Candidate Ceramic Nuclear Wasteforms

    Energy Technology Data Exchange (ETDEWEB)

    Vance, Eric R.; Carter, M. L.; Lumpkin, G. R.; Day, R. A.; Begg, B. D.

    2001-04-02

    This goal of this research project was to determine the solid solubility of Pu, U, Gd, and Hf in candidate ceramics for immobilization of high-level nuclear waste. The experimental approach was to saturate each phase by adding more than the solid solubility limit of the given cation, using a nominated substitution scheme, and then analyzing the candidate phase that formed to evaluate the solid solubility limit under firing conditions. Confirmation that the solid solution limit had been reached insofar as other phases rich in the cation of interest was also required. The candidate phases were monazite, titanite, zirconolite, perovskite, apatite, pyrochlore, and brannerite. The valences of Pu and U were typically deduced from the firing atmosphere, and charge balancing in the candidate phase composition as evaluated from electron microscopy, although in some cases it was measured directly by x-ray absorption and diffuse reflectance spectroscopies (for U). Tetravalent Pu and U have restricted (< 0.1 formula units) solid solubility in apatite, titanite, and perovskite. Trivalent Pu has a larger solubility in apatite and perovskite than Pu4+. U3+ appears to be a credible species in reduced perovskite with a solubility of {approximately} 0.25 f.u. as opposed to {approximately} 0.05 f.u. for U4+. Pu4+ is a viable species in monazite and is promoted at lower firing temperatures ({approximately} 800 C) in an air atmosphere. Hf solubility is restricted in apatite, monazite (< 0.1 f.u.), but is {approximately} 0.2 and 0.5 f.u. in brannerite and titanite, respectively. Gd solubility is extended in all phases except for titanite ({approximately} 0.3 f.u.). U5+ was identified by DRS observations of absorption bands in the visible/near infrared photon energy ranges in brannerite and zirconolite, and U4+ in zirconolite was similarly identified.

  4. (239)Pu fallout across continental Australia: Implications on (239)Pu use as a soil tracer.

    Science.gov (United States)

    Lal, R; Fifield, L K; Tims, S G; Wasson, R J

    2017-09-19

    At present there is a need for the development of new radioisotopes for soil erosion and sediment tracing especially as fallout (137)Cs levels become depleted. Recent studies have shown that (239)Pu can be a useful new soil erosion and sediment radioisotope tracer. (239)Pu was released in the major atmospheric nuclear weapons tests of 1950's and 1960's. However (239)Pu has a half-life of 24110 years and more than 99% of this isotope is still present in the environment today. In contrast (137)Cs with a half-life of 30.07 year has decayed to atom ratios range from 0.045 to 0.197, with averages of 0.139(0.017), 0.111(0.052) and 0.160(0.027) in the 10-20°S, 20-30°S and 30-40°S latitude bands respectively. The (240)Pu/(239)Pu atom ratios in Central Australia (0.069) likely represent fallout from the Australian tests which also have low (240)Pu/(239)Pu atom ratios i.e., Maralinga (0.113) and Montebello (0.045). The average ratios in the 20-30°S and 30-40° bands are closer to the global average (0.139 and 0.177 respectively when not including the close-in fallout data from the nuclear test sites) if the Australian test sites and Central Australian sites are neglected as they clearly represent the effects of close in fallout. Copyright © 2017 Elsevier Ltd. All rights reserved.

  5. PuPO4(cr, hyd.) Solubility Product and Pu3+ Complexes With Phosphate and Ethylenediaminetetraacetic Acid

    Energy Technology Data Exchange (ETDEWEB)

    Rai, Dhanpat; Moore, Dean A.; Felmy, Andrew R.; Rosso, Kevin M.; Bolton, Harvey

    2010-06-15

    To determine the solubility product of PuPO4(cr, hyd.) and the complexation constants of Pu(III) with phosphate and EDTA, the solubility of PuPO4(cr, hyd.) was investigated as a function of: 1) time and pH varying from 1.0 to 12.0 and at a fixed 0.00032 M phosphate concentration; 2) NaH2PO4 concentrations varying from 0.0001 M to 1.0 M and at a fixed pH value of 2.5; 3) time and pH varying from 1.3 to 13.0 at fixed concentrations of 0.00032 M phosphate and 0.0004 M or 0.002 M Na2H2EDTA; and 4) Na2H2EDTA concentrations varying from 0.00005 M to 0.0256 M at a fixed 0.00032 M phosphate concentration and at pH values of approximately 3.5, 10.6, and 12.6. A combination of solvent extraction and spectrophotometric techniques confirmed that the use of hydroquinone and Na2S2O4 helped maintain Pu as Pu(III). The solubility data were interpreted using Pitzer and SIT models, and both provided similar values for the solubility product of PuPO4(cr, hyd.) and for the formation constant of PuEDTA-. The log10 of the solubility product of PuPO4(cr, hyd.) (PuPO4(cr, hyd.) = Pu3+ + PO4 ) was determined to be –(24.42 ± 0.38). Pitzer modeling showed that phosphate interactions with Pu3+ were extremely weak and did not require any phosphate complexes (e.g., PuPO4(aq), PuH2PO42+, Pu(H2PO4)2+, Pu(H2PO4)3(aq), and Pu(H2PO4)4-), as proposed in existing literature, to explain the experimental data. SIT modeling, however, required the inclusion of PuH2PO42+ to explain the data in high NaH2PO4 concentrations; this illustrates the differences one can expect when using these two chemical models to interpret the data. As the Pu(III)-EDTA species, only PuEDTA- was needed to interpret the experimental data in a large range in pH values (1.3–12.9) and EDTA concentrations (0.00005–0.256 M). Calculations based on density functional theory support the existence of PuEDTA- (with prospective stoichiometry as Pu(OH2)3EDTA-) as the chemically and structurally stable species. The log10 of the

  6. PROPERTIES AND BEHAVIOR OF 238PU RELEVANT TO DECONTAMINATION OF BUILDING 235-F

    Energy Technology Data Exchange (ETDEWEB)

    Duncan, A.; Kane, M.

    2009-11-24

    1101) may offer significant advantages over conventional liquid decontamination solutions. Previous trials are discussed and have been used successfully at SRS on various surfaces. Some areas showed minimal improvement, while others presented complete (100%) decontamination. However, small scale testing is recommended prior to the full scale use in the cells of PuFF in building 235-F.

  7. A multi-radionuclide approach to evaluate the suitability of {sup 239+240}Pu as soil erosion tracer

    Energy Technology Data Exchange (ETDEWEB)

    Meusburger, Katrin, E-mail: Katrin.Meusburger@unibas.ch [Environmental Geosciences, University of Basel, Bernoullistrasse 30, CH-4056 Basel (Switzerland); Mabit, Lionel, E-mail: L.Mabit@iaea.org [Soil and Water Management and Crop Nutrition Laboratory, FAO/IAEA Agriculture & Biotechnology Laboratory, IAEA Laboratories, Seibersdorf (Austria); Ketterer, Michael, E-mail: mkettere@msudenver.edu [Chemistry Department, Metropolitan State University of Denver, CO (United States); Park, Ji-Hyung, E-mail: jhp@ewha.ac.kr [Department of Environmental Science & Engineering, Ewha Womans University, Seoul 120-750 (Korea, Republic of); Sandor, Tarjan [Radioanalytical Reference Laboratory, Central Agricultural Office Food and Feed Safety Directorate (Hungary); Porto, Paolo, E-mail: paolo.porto@unirc.it [Dipartimento di AGRARIA, Università degli Studi “Mediterranea” di Reggio Calabria (Italy); Alewell, Christine, E-mail: Christine.Alewell@unibas.ch [Environmental Geosciences, University of Basel, Bernoullistrasse 30, CH-4056 Basel (Switzerland)

    2016-10-01

    Fallout radionuclides have been used successfully worldwide as tracers for soil erosion, but relatively few studies exploit the full potential of plutonium (Pu) isotopes. Hence, this study aims to explore the suitability of the plutonium isotopes {sup 239}Pu and {sup 240}Pu as a method to assess soil erosion magnitude by comparison to more established fallout radionuclides such as {sup 137}Cs and {sup 210}Pb{sub ex}. As test area an erosion affected headwater catchment of the Lake Soyang (South Korea) was selected. All three fallout radionuclides confirmed high erosion rates for agricultural sites (> 25 t ha{sup −1} yr{sup −1}). Pu isotopes further allowed determining the origin of the fallout. Both {sup 240}Pu/{sup 239}Pu atomic ratios and {sup 239+240}Pu/{sup 137}Cs activity ratios were close to the global fallout ratio. However, the depth profile of the {sup 239+240}Pu/{sup 137}Cs activity ratios in undisturbed sites showed lower ratios in the top soil increments, which might be due to higher migration rates of {sup 239+240}Pu. The activity ratios further indicated preferential transport of {sup 137}Cs from eroded sites (higher ratio compared to the global fallout) to the depositional sites (smaller ratio). As such the {sup 239+240}Pu/{sup 137}Cs activity ratio offered a new approach to parameterize a particle size correction factor that can be applied when both {sup 137}Cs and {sup 239+240}Pu have the same fallout source. Implementing this particle size correction factor in the conversion of {sup 137}Cs inventories resulted in comparable estimates of soil loss for {sup 137}Cs and {sup 239+240}Pu. The comparison among the different fallout radionuclides highlights the suitability of {sup 239+240}Pu through less preferential transport compared to {sup 137}Cs and the possibility to gain information regarding the origin of the fallout. In conclusion, {sup 239+240}Pu is a promising soil erosion tracer, however, since the behaviour i.e. vertical migration in the

  8. {sup 238}Pu, {sup 239+240}Pu and {sup 241}Am levels in the terrestrial and aquatic environment of the Loire and Garonne rivers basins (France)

    Energy Technology Data Exchange (ETDEWEB)

    Rousseau, G.; Mokili, M.B.; Le Roy, C.; Pagano, V. [SUBATECH/IN2P3 (France); Gontier, G.; Boyer, C. [EDF-DPI-DIN-CIDEN (France); Chardon, P. [CNRS/IN2P3 (France); Hemidy, P.Y. [EDF-DPN-UNIE-GPRE-IEV (France)

    2014-07-01

    Plutonium and americium long-lived alpha emitter isotopes can be found in the environment because of atmospheric global fallout due to thermonuclear tests performed between 1945 and 1980, to the American SNAP 9A satellite explosion in 1964, to the Chernobyl nuclear power plant accident,... In France, the nuclear safety authority does not allow the release of artificial alpha emitters from nuclear power plants. Thus, monitoring is performed to verify the absence of these alpha emitters in liquid discharges to respect the limits set by the regulations. These thresholds ensure a very low dosimetric impact to the population compared to other radionuclides. With the objective of environmental monitoring around nuclear facilities, activity measurements of long-lived alpha emitters are carried out to detect the traces of these radionuclides. Analysis of low activity by alpha spectrometry after chemical steps were performed and used to determine the {sup 238}Pu, {sup 239+240}Pu and {sup 241}Am activities on a large set of environmental solid samples likely to be encountered in environmental monitoring as soils, sediments, terrestrial and aquatic bio-indicators. The samples collected in the terrestrial and aquatic environment of the Loire and Garonne rivers basins (France) was investigated for the 2009-2014 period. It was found that the mean activity concentration of the most frequently detected was for the radionuclide {sup 238}Pu: from <0.00031 to 0.0061 Bq/kg dry in terrestrial samples and from <0.00086 to 0.011 Bq/kg dry in aquatic samples; for the radionuclide {sup 239+240}Pu: from 0.00041 to 0.150 Bq/kg dry in terrestrial samples and from 0.0023 to 0.240 Bq/kg dry in aquatic samples and for the radionuclide {sup 241}Am: from <0.00086 to 0.087 Bq/kg dry in terrestrial samples and from 0.0022 to 0.120 Bq/kg dry in aquatic samples. {sup 238}Pu/{sup 239+240}Pu and {sup 241}Am/{sup 239+240}Pu ratios determined are in accordance with an environmental contamination due to

  9. Consistent Data Assimilation of Isotopes: 242Pu and 105Pd

    Energy Technology Data Exchange (ETDEWEB)

    G. Palmiotti; H. Hiruta; M. Salvatores

    2012-09-01

    In this annual report we illustrate the methodology of the consistent data assimilation that allows to use the information coming from integral experiments for improving the basic nuclear parameters used in cross section evaluation. A series of integral experiments are analyzed using the EMPIRE evaluated files for 242Pu and 105Pd. In particular irradiation experiments (PROFIL-1 and -2, TRAPU-1, -2 and -3) provide information about capture cross sections, and a critical configuration, COSMO, where fission spectral indexes were measured, provides information about fission cross section. The observed discrepancies between calculated and experimental results are used in conjunction with the computed sensitivity coefficients and covariance matrix for nuclear parameters in a consistent data assimilation. The results obtained by the consistent data assimilation indicate that not so large modifications on some key identified nuclear parameters allow to obtain reasonable C/E. However, for some parameters such variations are outside the range of 1 s of their initial standard deviation. This can indicate a possible conflict between differential measurements (used to calculate the initial standard deviations) and the integral measurements used in the statistical data adjustment. Moreover, an inconsistency between the C/E of two sets of irradiation experiments (PROFIL and TRAPU) is observed for 242Pu. This is the end of this project funded by the Nuclear Physics Program of the DOE Office of Science. We can indicate that a proof of principle has been demonstrated for a few isotopes for this innovative methodology. However, we are still far from having explored all the possibilities and made this methodology to be considered proved and robust. In particular many issues are worth further investigation: • Non-linear effects • Flexibility of nuclear parameters in describing cross sections • Multi-isotope consistent assimilation • Consistency between differential and integral

  10. Formation of Pu(III) colloids observed by laser-induced breakdown detection

    Energy Technology Data Exchange (ETDEWEB)

    Cho, H. R.; Cha, W.; Park, K. K.; Jung, E. C. [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

    2015-05-15

    In the present work, the reduction conditions were controlled through electrolysis. An electrochemical cell with a Teflon vessel and quartz tubes containing electrodes were installed in a glove-box purged with Ar gas to prepare plutonium samples at different pHs under reducing condition. The concentration of hydrogen ions (H{sup +}) of plutonium solutions was reduced using an electric current from a Ag/AgCl reference electrode to a Pt working electrode, which called coulometric pH titration. The electrolytic reducing condition maintains the dominant oxidation state of Pu(III). Soluble species were investigated using absorption spectroscopy adopting a liquid waveguide capillary cell (LWCC) which has an optical path length of 100 cm. The formation of plutonium hydroxide colloids and solubility were determined by laser-induced breakdown detection (LIBD). Electrolytic reduction was a useful method to investigate the hydrolysis, colloid formation and solubility of Pu(III) hydroxide. The oxidation state of Pu(III) maintained well during the reduction of hydrogen ions being comparable to strong reducing agents such as Fe powder. The determined solubility product was lower than the reported data by Felmy et al. . The existence of Pu(IV), which can result in lower solubility investigated by measurement of redox potentials of samples will be presented in detail.

  11. Adsorption behaviour of PuF6 on UO2F2 by the use of 236Pu

    Science.gov (United States)

    Sato, Nobuaki; Matsuda, Minoru; Mitsugashira, Toshiaki; Kirishima, Akira

    2010-03-01

    To know the behavior of plutonium in the fluoride volatility process (FLUOREX PROCESS) for the spent nuclear fuel, both UO2 and PuO2 are fluorinated by fluorine forming volatile UF6 and PuF6, respectively. Then PuF6 is separated and recovered from UF6 by using adsorption materials such as uranyl fluoride UO2F2. In this paper, adsorption behavior of PuF6on UO2F2 was examined by the use of 236Pu tracer. First, the stability of UO2F2 in F2atmosphere was analyzed by TG-DTA method showing that uranium volatilized completely over 350 °C by the formation of UF6 and the adsorption of plutonium by UO2F2 should be done at temperatures lower than 250 °C. The behavior of PtF6 as a chemical analogue of PuF6 was also conducted for comparison and it showed that the deposition of PtF4 on UO2F2 at 200 °C. When the 236Pu doped U3O8 was reacted with 10%F2-He gas, the PuF6 vaporized at ca. 600 °C. Then adsorption of 236Pu on UO2F2 was observed by α ray measurement. The adsorption mechanism of Pu on UO2F2 was discussed with experimental data and thermodynamic consideration.

  12. The implementation of SOMO (SOlution MOdeller) in the UltraScan analytical ultracentrifugation data analysis suite: enhanced capabilities allow the reliable hydrodynamic modeling of virtually any kind of biomacromolecule.

    Science.gov (United States)

    Brookes, Emre; Demeler, Borries; Rosano, Camillo; Rocco, Mattia

    2010-02-01

    The interpretation of solution hydrodynamic data in terms of macromolecular structural parameters is not a straightforward task. Over the years, several approaches have been developed to cope with this problem, the most widely used being bead modeling in various flavors. We report here the implementation of the SOMO (SOlution MOdeller; Rai et al. in Structure 13:723-734, 2005) bead modeling suite within one of the most widely used analytical ultracentrifugation data analysis software packages, UltraScan (Demeler in Modern analytical ultracentrifugation: techniques and methods, Royal Society of Chemistry, UK, 2005). The US-SOMO version is now under complete graphical interface control, and has been freed from several constraints present in the original implementation. In the direct beads-per-atoms method, virtually any kind of residue as defined in the Protein Data Bank (e.g., proteins, nucleic acids, carbohydrates, prosthetic groups, detergents, etc.) can be now represented with beads whose number, size and position are all defined in user-editable tables. For large structures, a cubic grid method based on the original AtoB program (Byron in Biophys J 72:408-415, 1997) can be applied either directly on the atomic structure, or on a previously generated bead model. The hydrodynamic parameters are then computed in the rigid-body approximation. An extensive set of tests was conducted to further validate the method, and the results are presented here. Owing to its accuracy, speed, and versatility, US-SOMO should allow to fully take advantage of the potential of solution hydrodynamics as a complement to higher resolution techniques in biomacromolecular modeling.

  13. {sup 69}Ga NMR in Pu{sub 1-x}Ga{sub x} (x < 0.01) alloy

    Energy Technology Data Exchange (ETDEWEB)

    Piskunov, Yu. [Institute of Metal Physics, Ural Branch of Russian Academy of Sciences, Kovalevskaya Str. 18, 620041 Ekaterinburg (Russian Federation)], E-mail: piskunov@imp.uran.ru; Mikhalev, K. [Institute of Metal Physics, Ural Branch of Russian Academy of Sciences, Kovalevskaya Str. 18, 620041 Ekaterinburg (Russian Federation); Zuev, Yu. [Russian Federal Nuclear Center, Institute of Technical Physics, Snezhinsk (Russian Federation); Verkhovskii, S.; Arkhipov, V. [Institute of Metal Physics, Ural Branch of Russian Academy of Sciences, Kovalevskaya Str. 18, 620041 Ekaterinburg (Russian Federation); Svyatov, I.; Podgornova, I.; Shestakov, A. [Russian Federal Nuclear Center, Institute of Technical Physics, Snezhinsk (Russian Federation); Ogloblichev, V.; Pogudin, A.; Buzlukov, A. [Institute of Metal Physics, Ural Branch of Russian Academy of Sciences, Kovalevskaya Str. 18, 620041 Ekaterinburg (Russian Federation)

    2007-10-11

    {sup 69}Ga nuclear magnetic resonance (NMR) experiments have been carried out on the Pu{sub 0.995}Ga{sub 0.005} alloy at temperatures between 20 and 420 K at magnetic field of 9.4 T to study the local charge symmetry and magnetic behavior of the Pu atoms surrounding solute Ga. In accordance with optical metallography and X-ray diffraction studies the investigated plates of alloy (20 mm x 3 mm x 0.2 mm) represent at room temperature the single {alpha}-phase material without any detectable macroscopic segregation of other phases (the corresponding volume fraction <0.03). It was revealed that the magnetic shift of the {sup 69}Ga NMR central line and the electric quadrupole broadening of the Ga NMR spectrum trace temperature dependence of the NMR parameters is observed for the {delta}-phase plutonium alloy Pu{sub 0.95}Ga{sub 0.05}. On the basis of {sup 69}Ga NMR and X-ray data obtained, it is suggested that specific microscopic areas with a size less than 100 nm exist in the {alpha}-phase plutonium alloys Pu{sub 0.995}Ga{sub 0.005}. The local charge and magnetic environment of the solute Ga in these microscopic areas are similar to the observed in the stabilized {delta}-Pu alloy.

  14. Study on reduction and back extraction of Pu(IV) by urea derivatives in nitric acid conditions

    Energy Technology Data Exchange (ETDEWEB)

    Ye, G.A.; Xiao, S.T.; Yan, T.H.; Lin, R.S.; Zhu, Z.W. [China Institute of Atomic Energy, P.O.Box 275(26), Beijing 102413 (China)

    2013-07-01

    The reduction kinetics of Pu(IV) by hydroxyl-semicarbazide (HSC), hydroxyurea (HU) and di-hydroxyurea (DHU) in nitric acid solutions were investigated separately with adequate kinetic equations. In addition, counter-current cascade experiments were conducted for Pu split from U in nitric acid media using three kinds of reductant, respectively. The results show that urea derivatives as a kind of novel salt-free reductant can reduce Pu(IV) to Pu(III) rapidly in the nitric acid solutions. The stripping experimental results showed that Pu(IV) in the organic phase can be stripped rapidly to the aqueous phase by the urea derivatives, and the separation factors of plutonium /uranium can reach more than 10{sup 4}. This indicates that urea derivatives is a kind of promising salt-free agent for uranium/plutonium separation. In addition, the complexing effect of HSC with Np(IV) was revealed, and Np(IV) can be back-extracted by HSC with a separation factor of about 20.

  15. The concentrations of 241Pu in the southern Baltic Sea

    Directory of Open Access Journals (Sweden)

    Strumińska-Parulska D. I.

    2013-04-01

    Full Text Available The aim of the work was 241Pu activities determination in different components (water, plankton and fish of the southern Baltic Sea ecosystem. The determination of 241Pu in the samples was done indirectly by activity measuring the increment in 241Am from the decay of β-emitting 241Pu in samples collected 10-15 years after the Chernobyl accident. Enhanced levels of 241Pu were observed in all analyzed Baltic samples. The plutonium is also non-uniformly distributed between the organs and tissues of the analyzed fish; especially pelagic herring and cod as well as benthic flounder. The annual individual effective doses calculated on the basis of 241Pu concentrations in fish indicated that the impact of the consumption of 241Pu with Baltic fish on the annual effective dose for a statistical inhabitant of Poland was very small.

  16. Iron Corrosion Observations: Pu(VI)-Fe Reduction Studies

    Energy Technology Data Exchange (ETDEWEB)

    Reed, Donald T. [Los Alamos National Laboratory; Swanson, Juliet S. [Los Alamos National Laboratory; Richmann, Michael K. [Los Alamos National Laboratory; Lucchini, Jean-Francois [Los Alamos National Laboratory; Borkowski, Marian [Los Alamos National Laboratory

    2012-09-11

    Iron and Pu Reduction: (1) Very different appearances in iron reaction products were noted depending on pH, brine and initial iron phase; (2) Plutonium was associated with the Fe phases; (3) Green rust was often noted at the higher pH; (4) XANES established the green rust to be an Fe2/3 phase with a bromide center; and (5) This green rust phase was linked to Pu as Pu(IV).

  17. /sup 238/Pu fuel-form processes. Quarterly report, October-December 1981

    Energy Technology Data Exchange (ETDEWEB)

    1982-05-01

    Progress in the Savannah River /sup 238/Pu Fuel Form Program is summarized. Work during this period concentrated on the extensive cracking of the /sup 238/PuO/sub 2/ fuel form prior to encapsulation in the iridium containment shell for heat sources. This cracking results in increased recycle cost and decreased production efficiency. To better understand this cracking, Savannah River Laboratory (SRL) has made an extensive review of the development of /sup 238/PuO/sub 2/ fuel forms from small-scale Multi-hundred Watt (MHW) pellets through the current GPHS full-scale pellet production. Historically, /sup 238/PuO/sub 2/ fuel has almost always been uncracked after hot pressing in a graphite die, but has emerged cracked and fragile from the final heat-treatment furnace. The cracking tendency depends on the microstructure of the fuel form and on the hot pressing conditions used to fabricate it. In general, a microstructure of large intershard porosity is more desirable because it allows internal gas to escape more readily and it can absorb more reoxidation strain. Studies of the GPHS microstructure showed that the internal structures of typical GPHS Pellets fabricated at LANL and in the PEF differed significantly. The LANL pellets had severe density gradients and were extensively cracked.

  18. New measurement of the 242Pu(n,γ) cross section at n_TOF

    Science.gov (United States)

    Lerendegui-Marco, J.; Guerrero, C.; Cortés-Giraldo, M. A.; Quesada, J. M.; Mendoza, E.; Cano-Ott, D.; Eberhardt, K.; Junghans, A.

    2016-03-01

    The use of MOX fuel (mixed-oxide fuel made of UO2 and PuO2) in nuclear reactors allows substituting a large fraction of the enriched Uranium by Plutonium reprocessed from spent fuel. With the use of such new fuel composition rich in Pu, a better knowledge of the capture and fission cross sections of the Pu isotopes becomes very important. In particular, a new series of cross section evaluations have been recently carried out jointly by the European (JEFF) and United States (ENDF) nuclear data agencies. For the case of 242Pu, the two only neutron capture time-of-flight measurements available, from 1973 and 1976, are not consistent with each other, which calls for a new time-of flight capture cross section measurement. In order to contribute to a new evaluation, we have perfomed a neutron capture cross section measurement at the n_TOF-EAR1 facility at CERN using four C6D6 detectors, using a high purity target of 95 mg. The preliminary results assessing the quality and limitations (background, statistics and γ-flash effects) of this new experimental data are presented and discussed, taking into account that the aimed accuracy of the measurement ranges between 7% and 12% depending on the neutron energy region.

  19. Evaluation of containment failure and cleanup time for Pu shots on the Z machine.

    Energy Technology Data Exchange (ETDEWEB)

    Darby, John L.

    2010-02-01

    Between November 30 and December 11, 2009 an evaluation was performed of the probability of containment failure and the time for cleanup of contamination of the Z machine given failure, for plutonium (Pu) experiments on the Z machine at Sandia National Laboratories (SNL). Due to the unique nature of the problem, there is little quantitative information available for the likelihood of failure of containment components or for the time to cleanup. Information for the evaluation was obtained from Subject Matter Experts (SMEs) at the Z machine facility. The SMEs provided the State of Knowledge (SOK) for the evaluation. There is significant epistemic- or state of knowledge- uncertainty associated with the events that comprise both failure of containment and cleanup. To capture epistemic uncertainty and to allow the SMEs to reason at the fidelity of the SOK, we used the belief/plausibility measure of uncertainty for this evaluation. We quantified two variables: the probability that the Pu containment system fails given a shot on the Z machine, and the time to cleanup Pu contamination in the Z machine given failure of containment. We identified dominant contributors for both the time to cleanup and the probability of containment failure. These results will be used by SNL management to decide the course of action for conducting the Pu experiments on the Z machine.

  20. New measurement of the 242Pu(n,γ cross section at n_TOF

    Directory of Open Access Journals (Sweden)

    Lerendegui-Marco J.

    2016-01-01

    Full Text Available The use of MOX fuel (mixed-oxide fuel made of UO2 and PuO2 in nuclear reactors allows substituting a large fraction of the enriched Uranium by Plutonium reprocessed from spent fuel. With the use of such new fuel composition rich in Pu, a better knowledge of the capture and fission cross sections of the Pu isotopes becomes very important. In particular, a new series of cross section evaluations have been recently carried out jointly by the European (JEFF and United States (ENDF nuclear data agencies. For the case of 242Pu, the two only neutron capture time-of-flight measurements available, from 1973 and 1976, are not consistent with each other, which calls for a new time-of flight capture cross section measurement. In order to contribute to a new evaluation, we have perfomed a neutron capture cross section measurement at the n_TOF-EAR1 facility at CERN using four C6D6 detectors, using a high purity target of 95 mg. The preliminary results assessing the quality and limitations (background, statistics and γ-flash effects of this new experimental data are presented and discussed, taking into account that the aimed accuracy of the measurement ranges between 7% and 12% depending on the neutron energy region.

  1. U, Pu, and Am nuclear signatures of the Thule hydrogen bomb debris

    DEFF Research Database (Denmark)

    Eriksson, Mats; Lindahl, Patric; Roos, Per

    2008-01-01

    ). In the five hot particles examined, the measured uranium atomic ratio was U-235/U-238 = 1.02 +/- 0.16 and the Pu-isotopic ratios were as follows: Pu-240/Pu-239 0.0551 +/- 0.0008 (atom ratio), Pu-238/Pu239+240 = 0.0161 +/- 0.0005 (activity ratio), Pu-241/Pu239+240 = 0.87 +/- 0.12 (activity ratio), and Am-241...... than one Pu source involved in the accident, confirming earlier studies. The Pu-238/Pu239+240 activity ratio and the Pu-240/Pu-239 atomic ratio were divided into at least two Pu-isotopic ratio groups. For both Pu-isotopic ratios, one ratio group had identical ratios as the five hot particles described...... above and for the other groups the Pu isotopic ratios were lower (Pu-238/Pu239+240 activity ratio similar to 0.01 and the Pu-240/Pu-239 atomic ratio 0.03). On the studied particles we observed that the U/Pu ratio decreased as a function of the time these particles were present in the sediment. We...

  2. Estimation of 240Pu Mass in a Waste Tank Using Ultra-Sensitive Detection of Radioactive Xenon Isotopes from Spontaneous Fission

    Energy Technology Data Exchange (ETDEWEB)

    Bowyer, Ted W. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Gesh, Christopher J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Haas, Derek A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Hayes, James C. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Mahoney, Lenna A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Meacham, Joseph E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Mendoza, Donaldo P. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Olsen, Khris B. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Prinke, Amanda M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Reid, Bruce D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Woods, Vincent T. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2014-12-01

    We report on a technique to detect and quantify the amount of 240Pu in a large tank used to store nuclear waste from plutonium production at the Hanford nuclear site. While the contents of this waste tank are known from previous grab sample measurements, our technique could allow for determination of the amount of 240Pu in the tank without costly sample retrieval and analysis of this highly radioactive material. This technique makes an assumption, which was confirmed, that 240Pu dominates the spontaneous fissions occurring in the tank.

  3. Statistical properties of $^{243}$Pu, and $^{242}$Pu(n,$\\gamma$) cross section calculation

    CERN Document Server

    Laplace, T A; Guttormsen, M; Larsen, A C; Bleuel, D L; Bernstein, L A; Goldblum, B L; Siem, S; Garotte, F L Bello; Brown, J A; Campo, L Crespo; Eriksen, T K; Giacoppo, F; Görgen, A; Hadyńska-Klȩk, K; Henderson, R A; Klintefjord, M; Lebois, M; Renstrøm, T; Rose, S J; Sahin, E; Tornyi, T G; Tveten, G M; Voinov, A; Wiedeking, M; Wilson, J N; Younes, W

    2015-01-01

    The level density and gamma-ray strength function (gammaSF) of 243Pu have been measured in the quasi-continuum using the Oslo method. Excited states in 243Pu were populated using the 242Pu(d,p) reaction. The level density closely follows the constant-temperature level density formula for excitation energies above the pairing gap. The gammaSF displays a double-humped resonance at low energy as also seen in previous investigations of actinide isotopes. The structure is interpreted as the scissors resonance and has a centroid of omega_{SR}=2.42(5)MeV and a total strength of B_{SR}=10.1(15)mu_N^2, which is in excellent agreement with sum-rule estimates. The measured level density and gammaSF were used to calculate the 242Pu(n,gamma) cross section in a neutron energy range for which there were previously no measured data.

  4. 239Pu(n,2n) 238Pu cross section inferred from IDA calculations and GEANIE measurements

    Energy Technology Data Exchange (ETDEWEB)

    Chen, H; Ormand, W E; Dietrich, F S

    2000-09-01

    This report presents the latest {sup 239}Pu(n,2n){sup 238}Pu cross sections inferred from calculations performed with the nuclear reaction-modeling code system, IDA, coupled with experimental measurements of partial {gamma}-ray cross sections for incident neutron energies ranging from 5.68 to 17.18 MeV. It is found that the inferred {sup 239}Pu(n,2n){sup 238}Pu cross section peaks at E{sub inc} {approx} 11.4 MeV with a peak value of approximately 326 mb. At E{sub inc} {approx} 14 MeV, the inferred {sup 239}Pu(n,2n){sup 238}Pu cross section is found to be in good agreement with previous radio-chemical measurements by Lockheed. However, the shape of the inferred {sup 239}Pu(n,2n){sup 238}Pu cross section differs significantly from previous evaluations of ENDL, ENDF/B-V and ENDF/B-VI. In our calculations, direct, preequilibrium, and compound reactions are included. Also considered in the modeling are fission and {gamma}-cascade processes in addition to particle emission. The main components of physics adopted and the parameters used in our calculations are discussed. Good agreement of the inferred {sup 239}Pu(n,2n){sup 238}Pu cross sections derived separately from IDA and GNASH calculations is shown. The two inferences provide an estimate of variations in the deduced {sup 239}Pu(n,2n){sup 238}Pu cross section originating from modeling.

  5. Microbially produced extracellular poly-saccharidic Pu(IV)- binding ligands

    Energy Technology Data Exchange (ETDEWEB)

    Hung, C.C.; Roberts, K.A.; Schwehr, K.A.; Santschi, P.H. [Texas A and M University at Galveston, 5007 Ave U, Galveston, TX 77551 (United States)

    2005-07-01

    Full text of publication follows: The investigation of the Pu-binding properties of ligands for diverse extracellular polysaccharides (EPS) is of relevance for the quantitative understanding of colloidal barriers to radionuclide migration. The EPS isolated for this study were from four different bacteria species: a) two aerobic soil bacteria: Shewanella putrefaciens CN32 and Pseudomonas fluorescens Biovar II; and b) one anaerobic bacterium, Clostridium sp. BC1. EPS from these bacteria were isolated through repeated ethanol precipitations. The neutral monosaccharides in the EPS from Pseudomonas florescens Biovar II that were determined by GC-MS consisted of rhamnose, fucose, ribose, arabinose, xylose, mannose, galactose and glucose. The potentially Pu(IV) binding EPS ligands were mainly composed of carboxylic acids and other minor poly-anionic groups, e.g., sulphates and phosphates. Up to 70 % of total carbohydrates were hydrophilic uronic acids, and total carbohydrates made up 23-31% of organic carbon for P. florescens Biovar II and 9-17% of organic carbon for S. putrefaciens CN32. Besides the neutral and acidic sugars in the EPS, there were also 2-13 % of more hydrophobic proteins among these bacterial EPS. Pu binding to these exo-polymers showed log Kd values of about 5 - 6, with results strongly dependent on procedural details (e.g., removal of colloids in Pu(IV) tracer and reagent solutions). We hypothesize that the relative hydrophobicity of the EPS ligands affects the outcome in ternary sorption studies with colloidal silica. Experiments with varying relative hydrophobicities of EPS will elucidate the different sorption strengths and/or attachment potentials of the Pu-binding ligands to inorganic surfaces. (authors)

  6. 242Pu as tracer for simultaneous determination of 237Np and 239,240Pu in environmental samples

    DEFF Research Database (Denmark)

    Chen, Q.J.; Dahlgaard, H.; Nielsen, S.P.;

    2002-01-01

    A procedure has been developed using Pu-242 as tracer for simultaneous determination of Np-237 and Pu-239,Pu-240 in environmental samples. The validity of the method has been demonstrated by ICPMS and alpha-spectroscopy for up to 10 gram soil and sediment, seawater up to 200 litres. The paper...... describes a suitable chemical procedure for Np and Pu including a quantitative pre-concentration of neptunium and plutonium, preparation of Np4+ and Pu4+, NP(NO3)(6)(2-) and Pu(NO3)(6)(2-), The ratio of Np-237/Pu-242 (or Np-237/Pu-239) before and after the procedure has been determined using 10 g soil (free...... from Np and Pu) R-before/R-after = 1.004 +/- 3.3% (S.D n = 20) and 1 litre seawater R-before/R-after = 1.019+/-1.9% (S.D., n = 12). Results from the intercomparison samples LAEA-135, LAEA-381 and from environmental samples are presented....

  7. Evaluation of fission cross sections and covariances for {sup 233}U, {sup 235}U, {sup 238}U, {sup 239}Pu, {sup 240}Pu, and {sup 241}Pu

    Energy Technology Data Exchange (ETDEWEB)

    Kawano, Toshihiko [Kyushu Univ., Fukuoka (Japan); Matsunobu, Hiroyuki [Data Engineering, Inc. (Japan); Murata, Toru [AITEL Corporation, Tokyo (JP)] [and others

    2000-02-01

    A simultaneous evaluation code SOK (Simultaneous evaluation on KALMAN) has been developed, which is a least-squares fitting program to absolute and relative measurements. The SOK code was employed to evaluate the fission cross sections of {sup 233}U, {sup 235}U, {sup 238}U, {sup 239}Pu, {sup 240}Pu, and {sup 241}Pu for the evaluated nuclear data library JENDL-3.3. Procedures of the simultaneous evaluation and the experimental database of the fission cross sections are described. The fission cross sections obtained were compared with evaluated values given in JENDL-3.2 and ENDF/B-VI. (author)

  8. Historical changes in 239Pu and 240Pu sources in sedimentary records in the East China Sea: Implications for provenance and transportation

    DEFF Research Database (Denmark)

    Wang, Jinlong; Baskaran, Mark; Hou, Xiaolin

    2017-01-01

    Concentrations and isotopic compositions of plutonium (Pu) are widely used for its source identification and to determine transport processes of Pu-associated particulate matter and water. We investigated the concentrations of 239Pu and 240Pu and their ratios in a number of sediment samples from...

  9. Is Octavalent Pu(VIII) Possible? Mapping the Plutonium Oxyfluoride Series PuO(n)F(8-2n) (n = 0-4).

    Science.gov (United States)

    Huang, Wei; Pyykkö, Pekka; Li, Jun

    2015-09-01

    While the oxidation state Pu(VIII) is shown to be less stable than Pu(V) in the PuO4 molecule, it is not clear if the more electronegative fluorine can help to stabilize Pu(VIII). Our calculations on PuO(n)F(8-2n) (n = 0-4) molecules notably confirm that PuO2F4 has both (1)D(4h) and (5)C(2v) minima with the oxidation states Pu(VIII) and Pu(V), respectively, with the latter having lower energy. The hybrid-DFT, CCSD(T), and CASSCF methods all give the same result. The results conform to a superoxide ligand when n ≥ 2. PuF8 in a (1)O(h) state can decompose to PuF6 and F2, and PuOF6 in a (1)C(2v) state also can break down to PuF6 and 1/2 O2. The Pu(VIII) anion PuO2F5(-) does have a D(5h) minimum, which also lies above a (5)C(2v) Pu(V) peroxide structure. However, the energy differences between the different minima are not large, indicating that metastable species with oxidation states higher than Pu(V) cannot be completely excluded.

  10. Development of Pu analysis in high active liquid waste. JASPAS JC-13

    Energy Technology Data Exchange (ETDEWEB)

    Jitsukata, Syu [Joyo Industry Co., Ltd., Tokai, Ibaraki (Japan); Kuno, Takehiko; Sato, Soichi; Ikeda, Hisashi [Japan Nuclear Cycle Development Inst., Tokai, Ibaraki (Japan). Tokai Works; Kurosawa, Akira [Japan Nuclear Fuel Co. Ltd., Tokyo (Japan)

    2001-05-01

    It has been required from IAEA to determine a small amount of plutonium in the high active liquid waste solutions (HALW) in the Tokai reprocessing plant. High performance spectrophotometer (HPSP), which could be obtained lower detection limit than conventional spectrophotometer, is studied to be applied the inspection and verification analysis. The results of applicability test are described in this report. -Cold Test- Neodium, showing an absorption peak near the absorption wavelength of plutonium (VI), was used as an alternative element to plutonium, in order to review the calculation method of the peak intensity. -Hot Test- Plutonium nitrate solution was used for the fundamental test of this method. Since the method is known to be influenced by acidity, suspended sludge and coexistent elements in a sample, each dependency was examined. It was found that measurement results varied about 14% at a nitric acid concentration of 2-4 mol/L. Sludge could be removed by filtration before the measurement. The effect of coexisting elements could be eliminated adjusting the optical balance between reference and sample beam intensity. In the case of measuring a low concentration plutonium solution, a ratio of the peak intensity to the background intensity (S/B ratio) was not enough to the measured low concentration of Plutonium. Therefore a method should be improved the S/B ratio by analyzing the obtained spectra. Data accumulation method, simple moving average method and Fourier transform analysis was tested. The results showed that a combination of the accumulated average method and the moving average method was the optimum method for the purpose. Linearity of the calibration curve was found between 0-11 mgPu/L. Synthetic sample solution, which simulated the actual constituents of the HALW with plutonium, showed a good linear relation at 0-11 mgPu/L. The detection limit for plutonium concentration was 0.07 mgPu/L. When the synthetic HALW solution containing plutonium was

  11. Nuclear characteristics of Pu fueled LWR and cross section sensitivities

    Energy Technology Data Exchange (ETDEWEB)

    Takeda, Toshikazu [Osaka Univ., Suita (Japan). Faculty of Engineering

    1998-03-01

    The present status of Pu utilization to thermal reactors in Japan, nuclear characteristics and topics and cross section sensitivities for analysis of Pu fueled thermal reactors are described. As topics we will discuss the spatial self-shielding effect on the Doppler reactivity effect and the cross section sensitivities with the JENDL-3.1 and 3.2 libraries. (author)

  12. Desarrollo de un videojuego Android : P.U Pets

    OpenAIRE

    García Canales, Jesús Miguel

    2013-01-01

    El proyecto P.U Pets se trata de un videojuego que será desarrollado para la plataforma Android y que constará de 5 fases/niveles completos. El projecte P.U Pets es tracta d'un videojoc que serà desenvolupat per a la plataforma Android i que constarà de 5 fases/nivells complets.

  13. GGA and LDA + U calculations of Pu phases

    Energy Technology Data Exchange (ETDEWEB)

    Bouchet, J. [CEA-DAM, Departement de Physique Theorique et Appliquee, Bruyeres-le-Chatel (France)], E-mail: johann.bouchet@cea.fr; Albers, R.C. [Theoretical Division, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Jomard, G. [CEA-DAM, Departement de Physique Theorique et Appliquee, Bruyeres-le-Chatel (France)

    2007-10-11

    The effect of correlations in Pu are studied using GGA and LDA + U. We have used the simplicity of an approximate {alpha} phase structure, which we call a pseudo structure, to understand the main differences between low and high temperatures phases of Pu. Our results show the importance of the local atomic environment.

  14. First-principles LDA + U calculations investigating the lattice contraction of face-centered cubic Pu hydrides

    Energy Technology Data Exchange (ETDEWEB)

    Ao, B.Y., E-mail: aobingyun24@yahoo.com.cn [Science and Technology on Surface Physics and Chemistry Laboratory, P.O. Box 718-35, Mianyang 621907 (China); Wang, X.L.; Shi, P.; Chen, P.H.; Ye, X.Q.; Lai, X.C. [Science and Technology on Surface Physics and Chemistry Laboratory, P.O. Box 718-35, Mianyang 621907 (China); Gao, T., E-mail: gaotao@scu.edu.cn [Institute of Atomic and Molecular Physics, Sichuan University, Chengdu 610065 (China)

    2012-05-15

    Plutonium metal can be loaded with hydrogen, which forms complicated solid solutions and compounds, and leads to significant changes in electronic structure. A first-principles pseudopotential plane wave method with added Hubbard parameter U was employed to investigate the electronic and structural properties of face-centered cubic Pu hydrides (PuH{sub x}, x = 2, 2.25, and 3). The decrease in calculated lattice parameters with increasing x is in reasonable agreement with experimental findings. Comparative analysis of the electronic-structure results for a series of PuH{sub x} compositions reveals that lattice contraction occurs due to enhanced chemical bonding and the size effects involving interstitial atoms. We find that the size effects are the driving force for the abnormal lattice contraction.

  15. Influence of humic acid on plutonium sorption to gibbsite. Determination of Pu-humic acid complexation constants and ternary sorption studies

    Energy Technology Data Exchange (ETDEWEB)

    Zimmerman, Trevor; Powell, Brian A. [Clemson Univ., Anderson, SC (United States). Environmental Engineering and Earth Sciences; Zavarin, Mavrik [Lawrence Livermore National Laboratory, Livermore, CA (United States). Glenn T. Seaborg Institute

    2014-10-01

    In this work stability constants describing Pu(IV), Th(IV), and Np(V) binding to Leonardite humic acid (HA) were determined using a discrete pK{sub a} model. A hybrid ultra-filtration/equilibrium dialysis, ligand exchange technique was used to generate the partitioning data. Ethylenediaminetetraacetic acid (EDTA) was used as a reference ligand to allow the aqueous chemistry of the Pu(IV)-HA system to be examined over a range of pH values, while minimizing the possibility of precipitation of Pu(IV). The conditional stability constant for Pu(IV) complexation with HA determined as part of this work is logβ{sub 112} = 6.76 ± 0.14 based on the equation: Pu{sup 4+} + HL3 + 2H{sub 2}O <-> Pu(OH){sub 2}L3{sup +} + 3H{sup +} where HA is represented by HL3 (a binding site on the HA with a pK{sub a} value of 7). This value is three orders of magnitude higher than the Th(IV)-HA constant and between six and eight orders of magnitude higher than the Np(V)-HA complex. The magnitude of the stability constants and the general trend of increasing complexation strength with increasing pH is consistent with previous observations. The Pu(IV)-HA stability constants were used to model sorption of Pu(IV) to gibbsite in the presence of HA. Assuming only aqueous Pu-HA complexes and AlOH-Pu surface complexes, the model was unable to predict the observed data which exhibited greater sorption at pH 4 relative to pH 6; a phenomenon which does not occur in the absence of HA. Therefore, this study demonstrates that ternary Pu-HA-gibbsite complexes may form under low pH conditions and exhibit greater sorption than that observed in the absence of HA. Although the presence of HA may increase the solubility/aqueous concentrations of Pu in the absence of a solid phase, formation of ternary complexes may indeed retard the subsurface migration of Pu. The corollary to this finding is that increased mobility may occur if the ternary surface complex forms on a mobile colloid rather than part of the

  16. Spatial distribution of (241)Am, (137)Cs, (238)Pu, (239,240)Pu and (241)Pu over 17 year periods in the Ravenglass saltmarsh, Cumbria, UK.

    Science.gov (United States)

    Oh, J-S; Warwick, P E; Croudace, I W

    2009-01-01

    Ninety five surface scrape samples were collected at the Ravenglass saltmarsh and analysed for radionuclides by alpha spectrometry ((238)Pu and (239,240)Pu), gamma spectrometry ((241)Am and (137)Cs) and liquid scintillation counting ((241)Pu). Both (241)Am and (137)Cs activities are compared with those reported by Horrill [1983. Concentrations and spatial distribution of radioactivity in an ungrazed saltmarsh. In: Coughtrey, P.J. (Ed.), Ecological Aspects of Radionuclide Release. British Ecological Society Special Publication No. 3. Blackwell, Oxford, pp. 119-215.] Significant decreases in activities for both radionuclides were observed which is caused by the declining levels of discharges from the Sellafield nuclear reprocessing plant since the 1980s. It has been concluded that the spatial distribution of these radionuclides are controlled by the tidal currents and the clay contents in the sediments. There is evidence of surface erosion of the saltmarsh and redistribution of radionuclides in the saltmarsh using isotopic ratios of measured Pu.

  17. Evaluations of Mechanisms for Pu Uptake and Retention within Spherical Resorcinol-Formaldehyde Resin Columns

    Energy Technology Data Exchange (ETDEWEB)

    Delegard, Calvin H. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Levitskaia, Tatiana G. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Fiskum, Sandra K. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2016-09-15

    The unexpected uptake and retention of plutonium (Pu) onto columns containing spherical resorcinol-formaldehyde (sRF) resin during ion exchange testing of Cs (Cs) removal from alkaline tank waste was observed in experiments at both the Pacific Northwest National Laboratory (PNNL) and the Savannah River National Laboratory (SRNL). These observations have raised concern regarding the criticality safety of the Cs removal unit operation within the low-activity waste pretreatment system (LAWPS). Accordingly, studies have been initiated at Washington River Protection Solutions (WRPS), who manages the operations of the Hanford Site tank farms, including the LAWPS, PNNL, and elsewhere to investigate these findings. As part of these efforts, PNNL has prepared the present report to summarize the laboratory testing observations, evaluate these phenomena in light of published and unpublished technical information, and outline future laboratory testing, as deemed appropriate based on the literature studies, with the goal to elucidate the mechanisms for the observed Pu uptake and retention.

  18. LDA + U study of Pu and PuO{sub 2} on ground state with spin-orbital coupling

    Energy Technology Data Exchange (ETDEWEB)

    Wang Hao, E-mail: haowangfp@gmail.com [International Research Center for Nuclear Materials Science, Institute for Materials Research, Tohoku University, Narita-cho 2145-2, Oarai-machi, Ibaraki, 311-1313 (Japan); Konashi, Kenji [International Research Center for Nuclear Materials Science, Institute for Materials Research, Tohoku University, Narita-cho 2145-2, Oarai-machi, Ibaraki, 311-1313 (Japan)

    2012-08-25

    Highlights: Black-Right-Pointing-Pointer In our paper, we use spin-orbital coupling to investigate PuO{sub 2}, which is the first time as our knowledge. Black-Right-Pointing-Pointer We also check initially the Jahn-Teller effect of PuO{sub 2}. Black-Right-Pointing-Pointer Based on the Bader charge analysis, the covalency of Pu and O atoms is clearly shown. - Abstract: In order to describe the structural, electronic and thermodynamic properties of {delta}-Pu and PuO{sub 2}, first-principle calculation is performed with spin-orbital coupling. By applying the DFT + U and occupation matrix method, we obtain a good result close to the experimental data. All possible initial occupation matrices are tried to find the ground state. The Jahn-Teller distortion and the spin-orbital effect are discussed. The intermediate coupling is proven by PDOS analysis. Covalency between Pu and O atoms is proven by quantum theory of atoms in molecules. By PDOS, occupation matrix and Bader charge analysis, the 5f configurations of {delta}-Pu and PuO{sub 2} are investigated.

  19. Oxidation states, geometries, and electronic structures of plutonium tetroxide PuO4 isomers: is octavalent Pu viable?

    Science.gov (United States)

    Huang, Wei; Xu, Wen-Hua; Su, Jing; Schwarz, W H E; Li, Jun

    2013-12-16

    In neutral chemical compounds, the highest known oxidation state of all elements in the Periodic Table is +VIII. While PuO4 is viewed as an exotic Pu(+VIII) complex, we have shown here that no stable electronic homologue of octavalent RuO4 and OsO4 exists for PuO4, even though Pu has the same number of eight valence electrons as Ru and Os. Using quantum chemical approaches at the levels of quasi-relativistic DFT, MP2, CCSD(T), and CASPT2, we find the ground state of PuO4 as a quintet (5)C2v-(PuO2)(+)(O2)(-) complex with the leading valence configuration of an (f(3))plutonyl(V) unit, loosely coupled to a superoxido (π*(3))O2(-) ligand. This stable isomer is likely detectable as a transient species, while the previously suggested planar (1)D4h-Pu(VIII)O4 isomer is only metastable. Through electronic structure analyses, the bonding and the oxidation states are explained and rationalized. We have predicted the characteristics of the electronic and vibrational spectra to assist future experimental identification of (PuO2)(+)(O2)(-) by IR, UV-vis, and ionization spectroscopy.

  20. Distinguishing Pu Metal from Pu Oxide and Determining alpha-ratio using Fast Neutron Counting

    Energy Technology Data Exchange (ETDEWEB)

    Verbeke, J. M. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Chapline, G. F. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Nakae, L. F. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Prasad, M. K. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Sheets, S. A. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Snyderman, N. J. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2015-01-07

    We describe a new method for determining the ratio of the rate of (α, n) source neutrons to the rate of spontaneous fission neutrons, the so called α-ratio. This method is made possible by fast neutron counting with liquid scintillator detectors, which can determine the shape of the fast neutron spectrum. The method utilizes the spectral difference between fission spectrum neutrons from Pu metal and the spectrum of (α, n) neutrons from PuO2. Our method is a generalization of the Cifarelli-Hage method for determining keff for fissile assemblies, and also simultaneously determines keff along with the α-ratio.

  1. Ostwald Ripening and Its Effect on PuO2 Particle Size in Hanford Tank Waste

    Energy Technology Data Exchange (ETDEWEB)

    Delegard, Calvin H.

    2011-09-29

    Between 1944 and 1989, the Hanford Site produced 60 percent (54.5 metric tons) of the United States weapons plutonium and produced an additional 12.9 metric tons of fuels-grade plutonium. High activity wastes, including plutonium lost from the separations processes used to isolate the plutonium, were discharged to underground storage tanks during these operations. Plutonium in the Hanford tank farms is estimated to be {approx}700 kg but may be up to {approx}1000 kg. Despite these apparent large quantities, the average plutonium concentration in the {approx}200 million liter tank waste volume is only about 0.003 grams per liter ({approx}0.0002 wt%). The plutonium is largely associated with low solubility metal hydroxide/oxide sludges where its low concentration and intimate mixture with neutron-absorbing elements (e.g., iron) are credited in nuclear criticality safety. However, concerns have been expressed that plutonium, in the form of plutonium hydrous oxide, PuO{sub 2} {center_dot} xH{sub 2}O, could undergo sufficient crystal growth through Ostwald ripening in the alkaline tank waste to potentially be separable from neutron absorbing constituents by settling or sedimentation. It was found that plutonium that entered the alkaline tank waste by precipitation through neutralization from acid solution is initially present as 2- to 3-nm (0.002- to 0.003-{mu}m) scale PuO{sub 2} {center_dot} xH{sub 2}O crystallite particles and grows from that point at exceedingly slow rates, posing no risk to physical segregation. These conclusions are reached by both general considerations of Ostwald ripening and specific observations of the behaviors of PuO{sub 2} and PuO{sub 2} {center_dot} xH{sub 2}O upon aging in alkaline solution.

  2. Goal functional evaluations for phase-field fracture using PU-based DWR mesh adaptivity

    Science.gov (United States)

    Wick, Thomas

    2016-06-01

    In this study, a posteriori error estimation and goal-oriented mesh adaptivity are developed for phase-field fracture propagation. Goal functionals are computed with the dual-weighted residual (DWR) method, which is realized by a recently introduced novel localization technique based on a partition-of-unity (PU). This technique is straightforward to apply since the weak residual is used. The influence of neighboring cells is gathered by the PU. Consequently, neither strong residuals nor jumps over element edges are required. Therefore, this approach facilitates the application of the DWR method to coupled (nonlinear) multiphysics problems such as fracture propagation. These developments then allow for a systematic investigation of the discretization error for certain quantities of interest. Specifically, our focus on the relationship between the phase-field regularization and the spatial discretization parameter in terms of goal functional evaluations is novel.

  3. Preparation and Properties of OMMT/PU Composites

    Directory of Open Access Journals (Sweden)

    Chen Yufei

    2015-01-01

    Full Text Available Prepolymer of polyurethane (PU was prepared by toluene diisocyanate (TDI and polyether diol through polymerization, organically modified montmorillonite (OMMT gained by montmorillonite (MMT that was modified by octadecyl trimethyl ammonium chloride (OTAC, and the OMMT was used as intercalator; alcohol-based OMMT/PU adhesive was synthesized. The micromorphology of OMMT/PU adhesives was observed by XRD, SEM, and AFM, and the shear strength, elongation at break, peel strength, and water resistance were tested and the relationship between structure and properties of the adhesives was observed and analyzed. XRD suggested that OMMT has been completely peeled in the polyurethane matrix and the spacing of layers has increased. SEM and AFM indicated that the OMMT dispersed evenly in the PU matrix and had a good transition with PU matrix, and the interface effects between two phases were strong. The results of the mechanical properties showed that OMMT could significantly help to improve properties of OMMT/PU adhesive, and the shearing strength, fracture tensile strength, and peel strength of 4 wt% OMMT/PU adhesive were 7.24 MPa, 2.14 MPa, and 451.2 N/m, respectively; the water absorption quantity was 2.82%. Compared with the unmodified PU, the shearing strength, tensile strength, and elongation at break of 4 wt% OMMT/PU adhesive were increased by 36.75%, 134.90%, and 76.80%, respectively. The peel strength decreased by 30.76%, and the water absorption decreased by 17.54%, in the meanwhile.

  4. Neutron powder diffraction study of 239PuD x

    Science.gov (United States)

    Bartscher, W.; Boeuf, A.; Caciuffo, R.; Fournier, J. M.; Haschke, J. M.; Manes, L.; Rebizant, J.; Rustichelli, F.; Ward, J. W.

    1985-05-01

    A neutron powder diffraction study has been carried out on several deuterids of Plutonium (PuD 2.25,PuD 2.33, PuD 2.65) to determine the positions of deuterium atoms in the host metal f.c.c. lattice. It has been found that vacancies occur in the tetrahedral sites. Moreover, with increasing deuterium concentration, octahedral interstitial deuterium atoms are displaced from their ideal positions. These results can be explained by the formation of clusters. Finally, at low temperature, these compounds become ferromagnetically ordered. An ordered magnetic moment μ 0≈0.8 μ B has been measured on all compounds.

  5. Elastic properties of gamma-Pu by resonant ultrasound spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Migliori, Albert [Los Alamos National Laboratory; Betts, J [Los Alamos National Laboratory; Trugman, A [Los Alamos National Laboratory; Mielke, C H [Los Alamos National Laboratory; Mitchell, J N [Los Alamos National Laboratory; Ramos, M [Los Alamos National Laboratory; Stroe, I [WORXESTER, MA

    2009-01-01

    Despite intense experimental and theoretical work on Pu, there is still little understanding of the strange properties of this metal. We used resonant ultrasound spectroscopy method to investigate the elastic properties of pure polycrystalline Pu at high temperatures. Shear and longitudinal elastic moduli of the {gamma}-phase of Pu were determined simultaneously and the bulk modulus was computed from them. A smooth linear and large decrease of all elastic moduli with increasing temperature was observed. We calculated the Poisson ratio and found that it increases from 0.242 at 519K to 0.252 at 571K.

  6. Decontamination of soils and materials containing medium-fired PuO{sub 2} using inhibited fluorides with polymer filtration technology

    Energy Technology Data Exchange (ETDEWEB)

    Temer, D.J.; Villarreal, R.; Smith, B.F. [Los Alamos National Lab., NM (United States)

    1997-10-01

    The decontamination of soils and/or materials from medium-fired plutonium oxide (PuO{sub 2}) with an effective and efficient decontamination agent that will not significantly dissolve the matrix requires a new and innovative technology. After testing several decontamination agents and solutions for dissolution of medium-fired PuO{sub 2}, the most successful decontamination solutions were fluoride compounds, which were effective in breaking the Pu-oxide bond but would not extensively dissolve soil constituents and other materials. The fluoride compounds, tetra fluoboric acid (HBF{sub 4}) and hydrofluorosilicic acid (H{sub 2}F{sub 6}Si), were effective in dissolving medium-fired PuO{sub 2}, and did not seem to have the potential to dissolve the matrix. In both compounds, the fluoride atom is attached to a boron or silicon atom that inhibits the reactivity of the fluoride towards other compounds or materials containing atoms less attracted to the fluoride atom in an acid solution. Because of this inhibition of the reactivity of the fluoride ion, these compounds are termed inhibited fluoride compounds or agents. Both inhibited fluorides studied effectively dissolved medium-fired PuO{sub 2} but exhibited a tendency to not attack stainless steel or soil. The basis for selecting inhibited fluorides was confirmed during leaching tests of medium-fired PuO{sub 2} spiked into soil taken from the Idaho National Engineering Laboratory (INEL). When dissolved in dilute HNO{sub 3}, HCl, or HBr, both inhibited fluoride compounds were effective at solubilizing the medium-fired PuO{sub 2} from spiked INEL soil.

  7. Determination of {sup 238}Pu, {sup 239+240}Pu, {sup 241}Pu and {sup 241}Am in radioactive waste from IPEN reactor

    Energy Technology Data Exchange (ETDEWEB)

    Geraldo, Bianca; Taddei, Maria Helena T.; Cheberle, Sandra M.; Ferreira, Marcelo T., E-mail: bgeraldo@cnen.gov.b, E-mail: mhtaddei@cnen.gov.b, E-mail: scsantos@cnen.gov.b, E-mail: ferreira@cnen.gov.b [Brazilian Nuclear Energy Commission (LAPOC/CNEN-MG), Pocos de Caldas, MG (Brazil). Lab. of Pocos de Caldas; Marumo, Julio T., E-mail: jtmarumo@ipen.b [Instituto de Pesquisas Energeticas e Nucleares (IPEN/CNEN-SP), Sao Paulo, SP (Brazil)

    2011-07-01

    Ion exchange resin is a common type of radioactive waste arising from treatment of coolant water of the main circuit of research and nuclear power reactors. This waste contains high concentrations of fission and activation products. The management of this waste includes its characterization in order to determine and quantify specific radionuclides including those known as difficult-to-measure radionuclides (RDM). The analysis of RDMs generally involves expensive and time-consuming complex radiochemical analysis for purification and separation of the radionuclides. The objective of this work is to show an easy methodology for quantifying plutonium and americium isotopes in spent ion exchange resin, used for purification of the cooling water of the IEA-R1 reactor located at the Nuclear and Energy Research Institute, IPEN-CNEN/SP. The resins were destroyed by acid digestion, followed by purification and separation of the Pu and Am isotopes with anionic and chromatographic resins. {sup 238}Pu, {sup 239}+{sup 24}'0Pu, and {sup 24}'1Am isotopes were analyzed in an alpha spectrometer equipped with surface barrier detectors. {sup 241}Pu isotope was analyzed by liquid scintillation counting. Chemical recovery yield ranged from 73 to 98% for Pu and 77 to 98% for Am, demonstrating that the methodology is suitable for identification and quantification of the isotopes studied in spent resins. (author)

  8. Absorption of caffeine in fermented Pu-er tea is inhibited in mice.

    Science.gov (United States)

    Huang, Ye-wei; Xu, Huan-huan; Wang, Su-min; Zhao, Yi; Huang, Yu-min; Li, Run-bo; Wang, Xuan-jun; Hao, Shu-mei; Sheng, Jun

    2014-07-25

    Caffeine is present in a number of dietary sources consumed worldwide. Although its pharmacokinetics has been intensively explored, little is known about complexed caffeine (C-CAF) in aqueous extraction of fermented Pu-er tea. The major components of C-CAF are oxidative tea polyphenols (OTP) and caffeine. Furthermore, the C-CAF can be precipitated in low pH solution. After administering the same amount of total caffeine and comparing the peak level of plasma caffeine with the coffee (contains 0.11 ± 0.01% C-CAF) group, the results showed that the caffeine/OTP (contains 66.67 ± 0.02% C-CAF) group and the instant Pu-er tea (contains 23.18 ± 0.02% C-CAF) group were 33.39% and 25.86% lower, respectively. The concentration of the metabolites of caffeine supports the idea that the absorption of the C-CAF was inhibited in mice. Congruent with this result, the amount of caffeine detected in mice excrement showed that more caffeine was eliminated in the caffeine/OTP group and the Pu-er tea group. The locomotor activity tests of mice demonstrated that the stimulating effect of caffeine in caffeine/OTP and Pu-er tea was weaker than in coffee. Our findings demonstrate that caffeine can be combined with OTP and the absorption of C-CAF is inhibited in mice, thus decreasing the irritation effect of caffeine. This may also be developed as a slow release formulation of caffeine.

  9. Determination of Pu-238 and Pu-239+240 in marine sediment samples of southern brazilian coast; Determinacao de Pu-238 e Pu-239+240 em amostras de sedimento marinho da costa sul brasileira

    Energy Technology Data Exchange (ETDEWEB)

    Figueira, Rubens C.L.; Cunha, Ieda Irma Lamas [Instituto de Pesquisas Energeticas e Nucleares (IPEN), Sao Paulo, SP (Brazil)]. E-mail: figueira@curiango.ipen.br; Furtado, Valdenir V.; Tessler, Moyses G. [Sao Paulo Univ., SP (Brazil). Inst. Oceanografico

    2000-07-01

    This work presents Pu-238 and Pu-239+240 levels from southern brazilian coast, in the region between Cabo de Santa Marta Grande (SC) and Cabo Frio (RJ), involving the seaside to external continental shelf. Pu-238 and Pu-239+240 levels in this region ranged from 15 to 150 mBq.kg{sup -1} and from 18.2 to 228 mBq.kg{sup -1}, respectively. The values are in agreement with the established range for south hemisphere as a result of the atmospheric fallout. The methodology for plutonium determination reached 30% to 75% as yield recovery and 4.2 mBq.kg{sup -1} as minimum detectable concentration (MDC). Thus the methodology is applicable to environmental samples analysis at low levels of the studied radionuclides. (author)

  10. [239Pu and chromosomal aberrations in human peripheral blood lymphocytes].

    Science.gov (United States)

    Okladnikova, N D; Osovets, S V; Kudriavtseva, T I

    2009-01-01

    The genome status in somatic cells was assessed using the chromosomal aberration (CA) test in peripheral blood lymphocytes from 194 plutonium workers exposed to occupational radiation mainly from low-transportable compounds of airborne 230Pu. Pu body burden at the time of cytogenetic study varied from values close to the method sensitivity to values multiply exceeding the permissible level. Standard (routine) methods of peripheral blood lymphocytes cultivation were applied. Chromatid- and chromosomal-type structural changes were estimated. Aberrations were estimated per 100 examined metaphase cells. The quantitative relationship between the CA frequency and Pu body burden and the absorbed dose to the lung was found. Mathematical processing of results was carried out based on the phenomenological model. The results were shown as theoretical and experimental curves. The threshold of the CA yield was 0.43 +/- 0.03 kBq (Pu body burden) and 6.12 +/- 1.20 cGy (absorbed dose to the lung).

  11. [ECG indices in dogs after inhalation of 239Pu].

    Science.gov (United States)

    Karpova, V N

    1985-11-01

    Dogs of both sexes aged 2 to 4 were subjected to inhalation inoculation with polymer 239Pu or submicron 239PuO2 aerosols in amounts close to acute, subacute and chronically effective ones. ECG was recorded in standard, amplified and single leads (V3). All calculations were done by lead II. Signs of the right heart overburdening were noted in the presence of the P-pulmonale complex, deep S1 wave or cardiac electrical axis of SI-SII-SIII type. Signs of the right heart overburdening were revealed after inhalation of polimer 239Pu (70%). The absence of similar changes in damage caused by 239Pu could be attributed to its fast resorption from the lungs resulting in more moderate lesion of the respiratory organs.

  12. Radiation enhanced diffusion in UO/sub 2/ and (U,Pu)O/sub 2/

    Energy Technology Data Exchange (ETDEWEB)

    Matzke, Hj. (Commission of the European Communities, Karlsruhe (Germany, F.R.). European Inst. for Transuranium Elements)

    1983-08-01

    The radiation enhanced diffusion (coefficient D*) of U-233 and Pu-238 in UO/sub 2/ and (U,Pu)O/sub 2/ with 2.5 and 15% Pu was measured during fission in a nuclear reactor. Normal diffusion sandwiches with a thin tracer layer were used. A radio-frequency furnace allowed the temperatures to be varied between 130 and 1400/sup 0/C. Neutron fluxes (7 x 10/sup 12/ to 1.2 x 10/sup 14/ n cm/sup -2/ s/sup -1/) and irradiation times (56 to 334 h) were also varied to cover ranges of fission rates (dF/dt) and of doses F between 4.2 x 10/sup 17/ and 3.1 x 10/sup 19/ f cm/sup -3/. Below approx. 1000/sup 0/C, D* was completely athermal and increased linearly with (dF/dt). It was described by D* = A(dF/dt) with A = 1.2 x 10/sup -29/ cm/sup 5/. A possible temperature dependence was indicated between approx. 1000 and 1200/sup 0/C. The results are explained in terms of thermal and pressure effects of fission spikes and are related with other studies of radiation damage as well as with technologically interesting processes occurring in UO/sub 2/ during irradiation.

  13. Geochemical association of Pu and Am in selected host-phases of contaminated soils from the UK and their susceptibility to chemical and microbiological leaching.

    Science.gov (United States)

    Kimber, Richard L; Corkhill, Claire L; Amos, Sean; Livens, Francis R; Lloyd, Jonathan R

    2015-04-01

    Understanding the biogeochemical behaviour and potential mobility of actinides in soils and groundwater is vital for developing remediation and management strategies for radionuclide-contaminated land. Pu is known to have a high Kd in soils and sediments, however remobilization of low concentrations of Pu remains a concern. Here, some of the physicochemical properties of Pu and the co-contaminant, Am, are investigated in contaminated soils from Aldermaston, Berkshire, UK, and the Esk Estuary, Cumbria, UK, to determine their potential mobility. Sequential extraction techniques were used to examine the host-phases of the actinides in these soils and their susceptibility to microbiological leaching was investigated using acidophilic sulphur-oxidising bacteria. Sequential extractions found the majority of (239,240)Pu associated with the highly refractory residual phase in both the Aldermaston (63.8-85.5 %) and Esk Estuary (91.9-94.5%) soils. The (241)Am was distributed across multiple phases including the reducible oxide (26.1-40.0%), organic (45.6-63.6%) and residual fractions (1.9-11.1%). Plutonium proved largely resistant to leaching from microbially-produced sulphuric acid, with a maximum 0.18% leached into solution, although up to 12.5% of the (241)Am was leached under the same conditions. If Pu was present as distinct oxide particles in the soil, then (241)Am, a decay product of Pu, would be expected to be physically retained in the particle. The differences in geochemical association and bioleachability of the two actinides suggest that this is not the case and hence, that significant Pu is not present as distinct particles. These data suggest the majority of Pu in the contaminated soils studied is highly recalcitrant to geochemical changes and is likely to remain immobile over significant time periods, even when challenged with aggressive "bioleaching" bacteria.

  14. Pu-doped zirconolite for minor actinide containment

    Energy Technology Data Exchange (ETDEWEB)

    Deschanels, X.; Broudic, V.; Jegou, C.; Peuget, S.; Roudil, D.; Jorion, F.; Advocat, T

    2004-07-01

    Zirconolite is a potential matrix for the immobilization of the minor actinides stream produced by the reprocessing of the spent fuel. In order to check the incorporation of actinide into the structure, zirconolite ceramic pellets doped with 10 wt% in {sup 239}PuO{sub 2} were sintered. Characterization by SEM, XRD and XANES spectroscopy have been done on this material. The microstructural homogeneity of the pellets is good, and their relative density is higher than 90% of the theoretical density. XANES spectroscopy shows that Pu is at the oxidation state IV in this material. To investigate the effects of radiation damage on zirconolite structure, pellets doped with 10 wt% of {sup 238}PuO{sub 2} were fabricated. The {sup 238}Pu accelerates the radiation damage relative to the {sup 239}Pu because of its much higher specific activity (63.2 x 10{sup 10} Bq/g for {sup 238}Pu vs. 2.2 x 10{sup 9} Bq/g for {sup 238}Pu). Some pellets are storing at ambient, 250 deg. C and 500 deg C. Up 10{sup 19} {alpha}/cm{sup 3}, the macroscopic swelling of the samples stored at ambient is about 0.5% by 10{sup 18} {alpha}/cm{sup 3}, and the microscopic one near 0.35% by 10{sup 18} {alpha}/cm{sup 3}. Some microcracks are observed on these pellets. The samples started to become amorphous at 10{sup 19} {alpha}/cm{sup 3}. The swelling strongly decreases with the storage temperature of the samples. The leaching rate of {sup 239}Pu doped ceramics measured by Soxhlet tests at 100 deg. C in deionized water appears to be the same as inactive material. (authors)

  15. Thermophysical properties and oxygen transport in the (U{sub x},Pu{sub 1−x})O{sub 2} lattice

    Energy Technology Data Exchange (ETDEWEB)

    Cooper, M.W.D. [Department of Materials, Imperial College London, London SW7 2AZ (United Kingdom); Murphy, S.T. [Department of Materials, Imperial College London, London SW7 2AZ (United Kingdom); Department of Physics and Astronomy, University College London, Gower Street, WC1E 6BT London (United Kingdom); Rushton, M.J.D. [Department of Materials, Imperial College London, London SW7 2AZ (United Kingdom); Grimes, R.W., E-mail: r.grimes@imperial.ac.uk [Department of Materials, Imperial College London, London SW7 2AZ (United Kingdom)

    2015-06-15

    Using molecular dynamics, the thermophysical properties of the (U{sub x},Pu{sub 1−x})O{sub 2} system have been investigated between 300 and 3200 K. The variation with temperature of lattice parameter, linear thermal expansion coefficient, enthalpy and specific heat at constant pressure, are explained in terms of defect formation and diffusivity on the oxygen sublattice. Vegard’s Law is approximately observed for the thermal expansion of the solid solutions below 2000 K. Deviation from Vegard’s Law above this temperature occurs due to the different superionic transition temperatures of the solid solutions (2200–2900 K). Similarly, a spike in the specific heat, associated with the superionic transition, occurs at lower temperatures in solid solutions that have a high Pu content. While oxygen diffusivity is higher in pure PuO{sub 2} than in pure UO{sub 2}, lower oxygen defect enthalpies in (U{sub x},Pu{sub 1−x})O{sub 2} solid solutions cause higher oxygen mobility than would be expected by interpolation between the diffusivities of the end members. In comparison to UO{sub 2} and PuO{sub 2} there is considerable variety of oxygen vacancy and oxygen interstitial sites in solid solutions generating a wide range of property values. Trends in the defect enthalpies are discussed in terms of composition and the lattice parameter of (U{sub x},Pu{sub 1−x})O{sub 2}. Comparison is made with previous work on (U{sub x},Th{sub 1−x})O{sub 2}.

  16. Single-cell analyses of regulatory network perturbations using enhancer-targeting TALEs suggest novel roles for PU.1 during haematopoietic specification.

    Science.gov (United States)

    Wilkinson, Adam C; Kawata, Viviane K S; Schütte, Judith; Gao, Xuefei; Antoniou, Stella; Baumann, Claudia; Woodhouse, Steven; Hannah, Rebecca; Tanaka, Yosuke; Swiers, Gemma; Moignard, Victoria; Fisher, Jasmin; Hidetoshi, Shimauchi; Tijssen, Marloes R; de Bruijn, Marella F T R; Liu, Pentao; Göttgens, Berthold

    2014-10-01

    Transcription factors (TFs) act within wider regulatory networks to control cell identity and fate. Numerous TFs, including Scl (Tal1) and PU.1 (Spi1), are known regulators of developmental and adult haematopoiesis, but how they act within wider TF networks is still poorly understood. Transcription activator-like effectors (TALEs) are a novel class of genetic tool based on the modular DNA-binding domains of Xanthomonas TAL proteins, which enable DNA sequence-specific targeting and the manipulation of endogenous gene expression. Here, we report TALEs engineered to target the PU.1-14kb and Scl+40kb transcriptional enhancers as efficient new tools to perturb the expression of these key haematopoietic TFs. We confirmed the efficiency of these TALEs at the single-cell level using high-throughput RT-qPCR, which also allowed us to assess the consequences of both PU.1 activation and repression on wider TF networks during developmental haematopoiesis. Combined with comprehensive cellular assays, these experiments uncovered novel roles for PU.1 during early haematopoietic specification. Finally, transgenic mouse studies confirmed that the PU.1-14kb element is active at sites of definitive haematopoiesis in vivo and PU.1 is detectable in haemogenic endothelium and early committing blood cells. We therefore establish TALEs as powerful new tools to study the functionality of transcriptional networks that control developmental processes such as early haematopoiesis.

  17. Estimation of uncertainties in resonance parameters of {sup 56}Fe, {sup 239}Pu, {sup 240}Pu and {sup 238}U

    Energy Technology Data Exchange (ETDEWEB)

    Nakagawa, Tsuneo; Shibata, Keiichi [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    1997-05-01

    Uncertainties have been estimated for the resonance parameters of {sup 56}Fe, {sup 239}Pu, {sup 240}Pu and {sup 238}U contained in JENDL-3.2. Errors of the parameters were determined from the measurements which the evaluation was based on. The estimated errors have been compiled in the MF32 of the ENDF format. The numerical results are given in tables. (author)

  18. Study of neutron-deficient isotopes of Fl in the 239Pu, 240Pu + 48Ca reactions

    Science.gov (United States)

    Voinov, A. A.; Utyonkov, V. K.; Brewer, N. T.; Oganessian, Yu Ts; Rykaczewski, K. P.; Abdullin, F. Sh; Dmitriev, S. N.; Grzywacz, R. K.; Itkis, M. G.; Miernik, K.; Polyakov, A. N.; Roberto, J. B.; Sagaidak, R. N.; Shirokovsky, I. V.; Shumeiko, M. V.; Tsyganov, Yu S.; Subbotin, V. G.; Sukhov, A. M.; Sabelnikov, A. V.; Vostokin, G. K.; Hamilton, J. H.; Stoyer, M. A.; Strauss, S. Y.

    2016-07-01

    The results of the experiments aimed at the synthesis of Fl isotopes in the 239Pu + 48Ca and 240Pu + 48Ca reactions are presented. The experiment was performed using the Dubna gas-filled recoil separator at the U400 cyclotron. In the 239Pu+48Ca experiment one decay of spontaneously fissioning 284Fl was detected at 245-MeV beam energy. In the 240Pu+48Ca experiment three decay chains of 285Fl were detected at 245 MeV and four decays were assigned to 284Fl at the higher 48Ca beam energy of 250 MeV. The α-decay energy of 285Fl was measured for the first time and decay properties of its descendants 281Cn, 277Ds, 273Hs, 269Sg, and 265Rf were determined more precisely. The cross section of the 239Pu(48Ca,3n)284Fl reaction was observed to be about 20 times lower than those predicted by theoretical models and 50 times less than the value measured in the 244Pu+48Ca reaction. The cross sections of the 240Pu(48Ca,4-3n)284,285Fl at both 48Ca energies are similar and exceed that observed in the reaction with lighter isotope 239Pu by a factor of 10. The decay properties of the synthesized nuclei and their production cross sections indicate rapid decrease of stability of superheavy nuclei with departing from the neutron number N=184 predicted to be the next magic number.

  19. On the electrochemical formation of Pu-Al alloys in molten LiCl-KCl

    Science.gov (United States)

    Mendes, E.; Malmbeck, R.; Nourry, C.; Souček, P.; Glatz, J.-P.

    2012-01-01

    Properties of Pu-Al alloys were investigated in connection with development of pyrochemical methods for reprocessing of spent nuclear fuel. Electroseparation techniques in molten LiCl-KCl are being developed in ITU to group-selectively recover actinides from the mixture with fission products. In the process, actinides are electrochemically reduced on solid aluminium cathodes, forming solid actinide-aluminium alloys. This article is focused on electro-chemical characterisation of Pu-Al alloys in molten LiCl-KCl, on electrodeposition of Pu on solid Al electrodes and on determination of chemical composition and structure of the formed alloys. Cyclic voltammetry and chronopotentiometry were used to study Pu-Al alloys in the temperature range 400-550 °C. Pu is reduced to metal in one reduction step Pu 3+/Pu 0 on an inert W electrode. On a reactive Al electrode, the reduction of Pu 3+ to Pu 0 occurs at a more positive potential due to formation of Pu-Al alloys. The open circuit potential technique was used to identify the alloys formed. Stable deposits were obtained by potentiostatic electrolyses of LiCl-KCl-PuCl 3 melts on Al plates. XRD and SEM-EDX analyses were used to characterise the alloys, which were composed mainly of PuAl 4 with some PuAl 3. In addition, the preparation of PuCl 3 containing salt by carbochlorination of PuO 2 is described.

  20. Ab initio equation-of-state and elastic properties of Pu metal and Pu-Ga alloys

    Science.gov (United States)

    Per, Soderlind; Landa, Alex

    2010-03-01

    We present results of ab initio calculations of equation-of-state and elastic properties for Pu metal and Pu-Ga alloys. For this we have employed density-functional theory (DFT) in conjunction with spin-orbit coupling and orbital polarization for the metal and coherent-potential approximation (CPA) for the alloys. All Pu systems benefit from spin polarization which is consistent with previous DFT studies of plutonium. We show that orbital correlations become more important proceeding from α->β->γ plutonium, thus suggesting increasing f-electron correlation (localization). For δ-Pu- Ga alloys we find that the system softens with larger Ga content, i.e., bulk modulus, elastic constants, and chemical bonding weakens with increasing Ga concentration. This inverse relationship is nearly linear and supported by measurements on polycrystal δ-Pu-Ga alloys. For Pu metal, our single-crystal results also relates reasonably with ultrasound data on polycrystal samples where available. The comparison is indirect but made possible by approximating the polycrystal with an isotropic (uniform strain) single crystal. This work performed under the auspices of the U.S. Department of Energy by Lawrence Livermore National Laboratory under Contract DE-AC52-07NA27344.

  1. Existence of bounded positive solutions of a nonlinear differential system

    Directory of Open Access Journals (Sweden)

    Sabrine Gontara

    2012-04-01

    Full Text Available In this article, we study the existence and nonexistence of solutions for the system $$displaylines{ frac{1}{A}(Au''=pu^{alpha }v^{s}quad hbox{on }(0,infty , cr frac{1}{B}(Bu''=qu^{r}v^{eta }quad hbox{on }(0,infty , cr Au'(0=0,quad u(infty =a>0, cr Bv'(0=0,quad v(infty =b>0, }$$ where $alpha ,eta geq 1$, $s,rgeq 0$, p,q are two nonnegative functions on $(0,infty $ and A, B satisfy appropriate conditions. Using potential theory tools, we show the existence of a positive continuous solution. This allows us to prove the existence of entire positive radial solutions for some elliptic systems.

  2. Ustur whole body case 0269: demonstrating effectiveness of i.v. CA-DTPA for Pu

    Energy Technology Data Exchange (ETDEWEB)

    James, A.C.; Sasser, L.B.; Stuit, D.B. [US Transuranium and Uranium Registries, College of Pharmacy, Washington State University, 1845 Terminal Drive, Suite 201, Richland, WA 99354 (United States); Glover, S.E. [Department of Mechanical, Industrial and Nuclear Engineering, University of Cincinnati, 598 Rhodes Hall, Cincinnati, OH 45221 (United States); Carbaugh, E.H. [Pacific Northwest National Laboratory, PO Box 999, Richland, WA 99354 (United States)

    2007-07-01

    This whole body donation case (USTUR Registrant) involved a single acute inhalation of an acidic Pu(NO{sub 3}){sub 4} solution in the form of an aerosol 'mist'. Chelation treatment with intravenously (i.v.) Ca-EDTA was initiated on the day of the intake, and continued intermittently over 6 months. After 2.5 y with no further treatment, a course of i.v. Ca-DTPA was administered. A total of 400 measurements of {sup 239+240}Pu excreted in urine were recorded; starting on the first day (both before and during the initial Ca-EDTA chelation) and continuing for 37 y. This sampling included all intervals of chelation. In addition, 91 measurements of {sup 239+240}Pu-in-feces were recorded over this whole period. The Registrant died about 38 y after the intake, at age 79 y, with extensive carcinomatosis secondary to adenocarcinoma of the prostate gland. At autopsy, all major soft tissue organs were harvested for radiochemical analyses of their {sup 238}Pu, {sup 239+240}Pu and {sup 241}Am content. Also, all types of bone (comprising about half the skeleton) were harvested for radiochemical analyses, as well as samples of skin, subcutaneous fat and muscle. This comprehensive data set has been applied to derive 'chelation-enhanced' transfer rates in the ICRP Publication 67 plutonium biokinetic model, representing the behaviour of blood-borne and tissue-incorporated plutonium during intervals of therapy. The resulting model of the separate effects of i.v. Ca-EDTA and Ca-DTPA chelation shows that the therapy administered in this case succeeded in reducing substantially the long-term burden of plutonium in all body organs, except for the lungs. The calculated reductions in organ content at the time of death are {approx}40% for the liver, 60% for other soft tissues (muscle, skin, glands, etc.), 50% for the kidneys and 50% for the skeleton. Essentially, all of the substantial reduction in skeletal burden occurred in trabecular bone. This modelling exercise

  3. USTUR WHOLE BODY CASE 0269: DEMONSTRATING EFFECTIVENESS OF I.V. CA-DTPA FOR PU

    Energy Technology Data Exchange (ETDEWEB)

    James, Anthony C.; Sasser , Lyle B.; Stuit, Dorothy B.; Glover, Samuel E.; Carbaugh, Eugene H.

    2008-01-28

    This whole body donation case (USTUR Registrant) involved a single acute inhalation of an acidic Pu(NO3)4 solution in the form of an aerosol ‘mist.’ Chelation treatment with i.v. Ca-EDTA was initiated on the day of the intake, and continued intermittently over 6 months. After 2½ years with no further treatment, a course of i.v. Ca-DTPA was administered. A total of 400 measurements of 239+240Pu excreted in urine were recorded; starting on the first day (both before and during the initial Ca-EDTA chelation), and continuing for 37 years. This sampling included all intervals of chelation. In addition, 91 measurements of 239+240Pu-in-feces were recorded over this whole period. The Registrant died about 38 years after the intake, at age 79 y, with extensive carcinomatosis secondary to adenocarcinoma of the prostate gland. At autopsy, all major soft tissue organs were harvested for radiochemical analyses of their 238Pu, 239+240Pu and 241Am content. Also, all types of bone (comprising about half the skeleton) were harvested for radiochemical analyses, as well as samples of skin, subcutaneous fat and muscle. This comprehensive dataset has been applied to derive ‘chelation-enhanced’ transfer rates in the ICRP Publication 67 plutonium biokinetic model, representing the behaviour of blood-borne and tissue-incorporated plutonium during intervals of therapy. The resulting model of the separate effects of i.v. Ca-EDTA and Ca-DTPA chelation shows that the therapy administered in this case succeeded in reducing substantially the long-term burden of plutonium in all body organs, except for the lungs. The calculated reductions in organ content at the time of death are approximately 40% for the liver, 60% for other soft tissues (muscle, skin, glands, etc.), 50% for the kidneys, and 50% for the skeleton. Essentially all of the substantial reduction in skeletal burden occurred in trabecular bone. This modeling exercise demonstrated that 3-y-delayed Ca-DTPA therapy was as

  4. Archiver ce qui aurait pu avoir lieu

    Directory of Open Access Journals (Sweden)

    Stefanie Baumann

    2009-12-01

    Full Text Available L’Atlas Group, un projet de l’artiste libanais Walid Raad, est « dédié à la recherche et la compilation de documents sur l’histoire contemporaine libanaise. L’Atlas Group produit, localise, conserve et étudie des documents visuels, sonores, textuels et autres, qui mettent en lumière l’histoire actuelle du Liban. »Ce projet est ainsi présenté comme une fondation qui génère des archives historiques et qui collecte des traces relevant de la guerre au Liban afin de les mettre à disposition aux chercheurs. Mais, les matériaux sont produits par l’artiste : l’archive est imaginaire, les documents et récits sont inventés, ainsi que le Docteur Fakhouhi, le personnage principal, présenté comme étant « le plus renommé des historiens au Liban ». Le spectateur se trouve alors devant un scénario très étrange dans lequel sont détournées les notions de document (qui peut désormais être aussi bien trouvé que produit et d’histoire (car les situations décrites sont considérées comme « ayant très bien pu avoir eu lieu », l’Atlas Group  les traite comme de véritables événement historiques et qui déplace, mine de rien, tout un dispositif. Au sein de ce projet, la frontière entre fiction et documentaire est complètement estompée : le geste de l’artiste (qui, lui, se présente comme une institution, un « Groupe », interroge ainsi le statut même d’auteur vise à la déplacer pour poser des questions relatives aux représentations possibles de l’histoire, aux personnes aptes à se charger de son écriture et à l’opération historiographique.

  5. Excess Pu disposition in zirconolite-rich Synroc containing nepheline

    Energy Technology Data Exchange (ETDEWEB)

    Vance, E.R.; Hart, K.P.; Day, R.A.; Begg, B.D.; Angel, P.J.; Loi, E.; Weir, J. [ANSTO, Menai, New South Wales (Australia); Oversby, V.M. [Lawrence Livermore Nation Lab., CA (United States)

    1996-08-01

    A titanate Synroc ceramic for the immobilization of Pu-bearing waste was designed to consist of 70 wt% zirconolite (CaZrTi{sub 2}O{sub 7}) + 15 wt% nepheline (NaAlSiO{sub 4}) + 15 wt% rutile (TiO{sub 2}). It contained 10 wt% of Pu plus 6 wt% of Gd as a neutron poison. The material was made by the standard sol-gel route, using a mixture of alkoxides and nitrates, followed by stir-drying and calcination. It was fabricated by hot-pressing at 1,150--1,250 C/20 MPa for 2 hours in a collapsible metal bellows. Though zirconolite was the majority phase, {approximately} 20 wt% of perovskite also formed. Some of the Na, intended for nepheline, partitioned into the titanate phases. 84-day differential total leach rates of Pu were in the order of 10{sup {minus}5} g/m{sup 2}/d at 90 and 200 C. Companion ceramics using molar substitution of Ce for Pu confirmed the idea that Ce is a good simulant of Pu from a solid state chemical view, but that there are limitations in terms of leach rate parallels.

  6. The I-Pu-Xe age of the Moon

    Science.gov (United States)

    Swindle, T. D.; Caffee, M. W.; Hohenberg, C. M.

    1984-01-01

    The Rb-Sr analyses of some lunar samples which indicate that the Moon is close to the age of primitive meteorites are only reliable to within about 100 m.y. A potentially more precise chronometer is the I-Pu-Xe system. I129 has a 17 m.y. halflife and decays to Xe129; Pu244, with an 82 m.y. halflife, produces Xe131 to Xe136 in fission. The I129/Pu244 ratio has a halflife of 21 m.y. Xenon retention for the Earth could have begun as late as the event that gave birth to the Moon. For the Moon, it is hard to imagine that xenon retention could have begun before re-accretion of the fissioned (and initially dispersed?) material, particularly if that material got hot enough to account for the depletion of the volatile elements. Thus, if fission model are correct, xenon retention in the Earth certainly began no later than in the Moon, and possibly began earlier. Therefore, the I-Pu-Xe system is only marginally consistent with a fission origin. If further study confirms that the I/U ratio of the Moon is .01 or less, or if gas-rich lunar highland breccias with higher ratios of I129 to Pu244 are found, it would be difficult to explain the results in an earth-fission model of lunar origin.

  7. Pu(V) transport through Savannah River Site soils - an evaluation of a conceptual model of surface- mediated reduction to Pu (IV).

    Science.gov (United States)

    Powell, Brian A; Kaplan, Daniel I; Serkiz, Steven M; Coates, John T; Fjeld, Robert A

    2014-05-01

    Over the last fifteen years the Savannah River Site (SRS) in South Carolina, USA, was selected as the site of three new plutonium facilities: the Mixed Oxide Fuel Fabrication Facility, Pit Disassembly and Conversion Facility, and the Pu Immobilization Plant. In order to assess the potential human and environmental risk associated with these recent initiatives, improved understanding of the fate and transport of Pu in the SRS subsurface environment is necessary. The hypothesis of this study was that the more mobile forms of Pu, Pu(V) and Pu(VI), would be reduced to the less mobile Pu(III/IV) oxidation states under ambient SRS subsurface conditions. Laboratory-scale dynamic flow experiments (i.e., column studies) indicated that Pu(V) was very mobile in SRS sediments. At higher pH values the mobility of Pu decreased and the fraction of Pu that became irreversibly sorbed to the sediment increased, albeit, only slightly. Conversely, these column experiments showed that Pu(IV) was essentially immobile and was largely irreversibly sorbed to the sediment. More than 100 batch sorption experiments were also conducted with four end-member sediments, i.e., sediments that include the chemical, textural, and mineralogical properties likely to exist in the SRS. These tests were conducted as a function of initial Pu oxidation state, pH, and contact time and consistently demonstrated that although Pu(V) sorbed initially quite weakly to sediments, it slowly, over the course of Pu(IV). This is consistent with our hypothesis that Pu(V) is reduced to the more strongly sorbing form of Pu, Pu(IV). These studies provide important experimental support for a conceptual geochemical model for dissolved Pu in a highly weathered subsurface environment. That is that, irrespective of the initial oxidation state of the dissolved Pu introduced into a SRS sediment system, Pu(IV) controls the environmental transport within a couple weeks and Pu strongly binds to the sediment, limiting its mobility.

  8. Characterization of a neutron source of {sup 239}PuBe; Caracterizacion de una fuente de neutrones de {sup 239}PuBe

    Energy Technology Data Exchange (ETDEWEB)

    Hernandez V, R.; Chacon R, A.; Hernandez D, V. M.; Mercado, G. A.; Vega C, H. R. [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Calle Cipres No. 10, Fracc. La Penuela, 98068 Zacatecas (Mexico); Ramirez G, J. [Instituto Nacional de Estadistica Geografia e Informatica, Direccion General de Innovacion y Tecnologia de Informacion, Av. Heroes de Nacozari Sur 2301, Fracc. Jardines del Parque, 20276 Aguascalientes (Mexico)], e-mail: ruben_zac@yahoo.com

    2009-10-15

    The spectrum equivalent dose and environmental equivalent dose f a {sup 239}PuBe source have been determined. The appropriate handling of a neutron source depends on the knowledge of its characteristics, such as its energy distribution, total rate of flowing and dosimetric magnitudes. In many facilities have not spectrometer that allows to determine the spectrum and then area monitors are used that give a dosimetric magnitude starting from measuring the flowing rate and the use of conversion factors, however this procedure has many limitations and it is preferable to measure the spectra and starting from this information the interest dosimetric magnitudes are calculated. In this work a Bonner sphere spectrometer has been used with a {sup 6}LiI(Eu) scintillator obtaining the count rates that produce, to a distance of 100 cm, a {sup 239}PuBe source of 1.85E(11) Bq. The spectrum was reconstructed starting from the count rates using BUNKIUT code and response matrix UTA4. With the spectrum information was calculated the source intensity, total flow, energy average, equivalent dose rate, environmental equivalent dose rate, equivalent dose coefficient and environmental equivalent dose coefficient. By means of two area monitors for neutrons, Eberline ASP-1 and LB 6411 of Berthold the equivalent dose and environmental equivalent dose were measured. The determinate values were compared with those reported in literature and it found that are coincident inside 17%. (Author)

  9. Alpha and conversion electron spectroscopy of 238,239Pu and 241Am and alpha-conversion electron coincidence measurements

    Energy Technology Data Exchange (ETDEWEB)

    Dion, Michael P.; Miller, Brian W.; Warren, Glen A.

    2016-09-01

    A technique to determine the isotopics of a mixed actinide sample has been proposed by measuring the coincidence of the alpha particle during radioactive decay with the conversion electron (or Auger) emitted during the relaxation of the daughter isotope. This presents a unique signature to allow the deconvolution of isotopes that possess overlapping alpha particle energy. The work presented here are results of conversion electron spectroscopy of 241Am, 238Pu and 239Pu using a dual-stage peltier-cooled 25 mm2 silicon drift detector. A passivated ion implanted planar silicon detector provided measurements of alpha spectroscopy. The conversion electron spectra were evaluated from 20–55 keV based on fits to the dominant conversion electron emissions, which allowed the relative conversion electron emission intensities to be determined. These measurements provide crucial singles spectral information to aid in the coincident measurement approach.

  10. ICE1 of Pyrus ussuriensis functions in cold tolerance by enhancing PuDREBa transcriptional levels through interacting with PuHHP1

    Science.gov (United States)

    Huang, Xiaosan; Li, Kongqing; Jin, Cong; Zhang, Shaoling

    2015-12-01

    ICE1 transcription factor plays an important role in plant cold stress via regulating the expression of stress-responsive genes. In this study, a PuICE1 gene isolated from Pyrus ussuriensis was characterized for its function in cold tolerance. The expression levels of the PuICE1 were induced by cold, dehydration and salt, with the greatest induction under cold conditions. PuICE1 was localized in the nucleus and could bind specifically to the MYC element in the PuDREBa promoter. The PuICE1 fused to the GAL4 DNA-binding domain to have transcriptional activation activity. Ectopic expression of the PuICE1 in tomato conferred enhanced tolerance to cold stress at cold temperatures, less electrolyte leakage, less MDA content, higher chlorophyll content, higher survival rate, higher proline content, higher activities of enzymes. In additon, steady-state mRNA levels of six stress-responsive genes coding for either functional or regulatory genes were induced to higher levels in the transgenic lines by cold stress. Yeast two-hybrid, transient assay, split luciferase complementation and BiFC assays all revealed that PuHHP1 protein can physically interact with PuICE1. Taken together, these results demonstrated that PuICE1 plays a positive role in cold tolerance, which may be due to enhancement of PuDREBa transcriptional levels through interacting with the PuHHP1.

  11. U, Pu, and Am nuclear signatures of the Thule hydrogen bomb debris.

    Science.gov (United States)

    Eriksson, Mats; Lindahl, Patric; Roos, Per; Dahlgaard, Henning; Holm, Elis

    2008-07-01

    This study concerns an arctic marine environment that was contaminated by actinide elements after a nuclear accident in 1968, the so-called Thule accident In this study we have analyzed five isolated hot particles as well as sediment samples containing particles from the weapon material for the determination of the nuclear fingerprint of the accident. We report that the fissile material in the hydrogen weapons involved in the Thule accident was a mixture of highly enriched uranium and weapon-grade plutonium and that the main fissile material was 235U (about 4 times more than the mass of 239Pu). In the five hot particles examined, the measured uranium atomic ratio was 235U/238U = 1.02 +/- 0.16 and the Pu-isotopic ratios were as follows: 24Pu/239Pu = 0.0551 +/- 0.0008 (atom ratio), 238Pu/239+240Pu = 0.0161 +/- 0.0005 (activity ratio), 241Pu/239+240Pu = 0.87 +/- 0.12 (activity ratio), and 241Am/ 239+240Pu = 0.169 +/- 0.005 (activity ratio) (reference date 2001-10-01). From the activity ratios of 241Pu/241Am, we estimated the time of production of this weapon material to be from the late 1950s to the early 1960s. The results from reanalyzed bulk sediment samples showed the presence of more than one Pu source involved in the accident, confirming earlier studies. The 238Pu/239+240PU activity ratio and the 240Pu/ 239Pu atomic ratio were divided into at least two Pu-isotopic ratio groups. For both Pu-isotopic ratios, one ratio group had identical ratios as the five hot particles described above and for the other groups the Pu isotopic ratios were lower (238Pu/ 239+240PU activity ratio approximately 0.01 and the 240Pu/P239Pu atomic ratio 0.03). On the studied particles we observed that the U/Pu ratio decreased as a function of the time these particles were present in the sediment. We hypothesis that the decrease in the ratio is due to a preferential leaching of U relative to Pu from the particle matrix.

  12. Optimal Bidding and Operation of a Power Plant with Solvent-Based Carbon Capture under a CO2 Allowance Market: A Solution with a Reinforcement Learning-Based Sarsa Temporal-Difference Algorithm

    Directory of Open Access Journals (Sweden)

    Ziang Li

    2017-04-01

    Full Text Available In this paper, a reinforcement learning (RL-based Sarsa temporal-difference (TD algorithm is applied to search for a unified bidding and operation strategy for a coal-fired power plant with monoethanolamine (MEA-based post-combustion carbon capture under different carbon dioxide (CO2 allowance market conditions. The objective of the decision maker for the power plant is to maximize the discounted cumulative profit during the power plant lifetime. Two constraints are considered for the objective formulation. Firstly, the tradeoff between the energy-intensive carbon capture and the electricity generation should be made under presumed fixed fuel consumption. Secondly, the CO2 allowances purchased from the CO2 allowance market should be approximately equal to the quantity of CO2 emission from power generation. Three case studies are demonstrated thereafter. In the first case, we show the convergence of the Sarsa TD algorithm and find a deterministic optimal bidding and operation strategy. In the second case, compared with the independently designed operation and bidding strategies discussed in most of the relevant literature, the Sarsa TD-based unified bidding and operation strategy with time-varying flexible market-oriented CO2 capture levels is demonstrated to help the power plant decision maker gain a higher discounted cumulative profit. In the third case, a competitor operating another power plant identical to the preceding plant is considered under the same CO2 allowance market. The competitor also has carbon capture facilities but applies a different strategy to earn profits. The discounted cumulative profits of the two power plants are then compared, thus exhibiting the competitiveness of the power plant that is using the unified bidding and operation strategy explored by the Sarsa TD algorithm.

  13. A licence to vape: Is it time to trial of a nicotine licensing scheme to allow Australian adults controlled access to electronic cigarettes devices and refill solutions containing nicotine?

    Science.gov (United States)

    Gartner, Coral; Hall, Wayne

    2015-06-01

    Australia has some of the most restrictive laws concerning use of nicotine in e-cigarettes. The only current legal option for Australians to legally possess and use nicotine for vaping is with a medical prescription and domestic supply is limited to compounding pharmacies that prepare medicines for specific patients. An alternative regulatory option that could be implemented under current drugs and poisons regulations is a 'nicotine licensing' scheme utilising current provisions for 'dangerous poisons'. This commentary discusses how such a scheme could be used to trial access to nicotine solutions for vaping outside of a 'medicines framework' in Australia.

  14. DISSOLUTION OF PLUTONIUM METAL USING NITRIC ACID SOLUTIONS CONTAINING POTASSIUM FLUORIDE

    Energy Technology Data Exchange (ETDEWEB)

    Rudisill, T.; Crowder, M.; Bronikowski, M.

    2007-10-15

    The deinventory and deactivation of the Savannah River Site's (SRS's) FB-Line facility required the disposition of approximately 2000 items from the facility's vaults. Plutonium (Pu) scraps and residues which do not meet criteria for conversion to a mixed oxide fuel will be dissolved and the solution stored for subsequent disposition. Some of the items scheduled for dissolution are composite materials containing Pu and tantalum (Ta) metals. The preferred approach for handling this material is to dissolve the Pu metal, rinse the Ta metal with water to remove residual acid, and burn the Ta metal. The use of a 4 M nitric acid (HNO{sub 3}) solution containing 0.2 M potassium fluoride (KF) was initially recommended for the dissolution of approximately 500 g of Pu metal. However, prior to the use of the flowsheet in the SRS facility, a new processing plan was proposed in which the feed to the dissolver could contain up to 1250 g of Pu metal. To evaluate the use of a larger batch size and subsequent issues associated with the precipitation of plutonium-containing solids from the dissolving solution, scaled experiments were performed using Pu metal and samples of the composite material. In the initial experiment, incomplete dissolution of a Pu metal sample demonstrated that a 1250 g batch size was not feasible in the HB-Line dissolver. Approximately 45% of the Pu was solubilized in 4 h. The remaining Pu metal was converted to plutonium oxide (PuO{sub 2}). Based on this work, the dissolution of 500 g of Pu metal using a 4-6 h cycle time was recommended for the HB-Line facility. Three dissolution experiments were subsequently performed using samples of the Pu/Ta composite material to demonstrate conditions which reduced the risk of precipitating a double fluoride salt containing Pu and K from the dissolving solution. In these experiments, the KF concentration was reduced from 0.2 M to either 0.15 or 0.175 M. With the use of 4 M HNO{sub 3} and a reduction in

  15. Characterization and Pervaporation Properties of Modified PU Membranes

    Directory of Open Access Journals (Sweden)

    Ye Hong

    2015-01-01

    Full Text Available Pervaporation will have broad application prospects in the treatment of phenolic wastewater. Polyurethane (PU membrane is promising but needs to be further modified. In this study, both β-CD and CNT were used to modify the PU membrane. The structure and property of these membranes were characterized by FTIR, DSC and TGA. The pervaporation performances were investigated, and the effects of β-CD and CNT on membrane separation were discussed. TGA shows that three kinds of modified membranes have enough thermal stability to afford pervaporation test and start weight loss at about 200 °C. In pervaporaiton, the total flux, separation factor and PSI value all increase with increased feed temperature. That is anti-trade-off phenomenon. Among these membranes, HTPB+β-CD-PU shows the best comprehensive performance at 80°C and has great potential for further application.

  16. Deducing the 236Pu(n,f) and 237Pu(n,f) cross sections via the surrogate ratio method

    Science.gov (United States)

    Hughes, R. O.; Beausang, C. W.; Ross, T. J.; Burke, J. T.; Casperson, R. J.; McCleskey, M.; Cooper, N.; Escher, J. E.; Gell, K. B.; Good, E.; Humby, P.; Saastimoinen, A.; Tarlow, T. D.

    2013-10-01

    The short half-lives associated with certain minor actinide nuclei that are relevant to stockpile stewardship pursuits and the development of next-generation nuclear reactors make direct neutron measurements very challenging. In certain cases, a stable beam and target ``surrogate reaction'' can be used in lieu of the neutron-induced reaction, and the (n,f) cross section can then be deduced indirectly. Agreement between surrogate and direct measurements for (n,f) cross sections in actinide nuclei is usually within 10%. The present work reports on the measurement of the 236Pu(n,f) and 237Pu(n,f) cross sections via 239Pu(p,tf) and 239Pu(p,df) surrogate reactions, respectively. The experiment was performed at the Texas A&M University Cyclotron Facility using a 28.5 MeV proton beam to bombard 239Pu and 235U targets. Outgoing light ions were detected in coincidence with fission fragments using the STAR-LiTe detector array. Results of the analysis will be presented. This work was supported by DoE Grant Numbers: DE-FG52-09NA29454 and DE-FG02-05ER41379 (Richmond), DE-AC52-07NA27344 (LLNL) and DE-FG52-09NA29467 (TAMU).

  17. Transuranic concentrations in reef and pelagic fish from the Marshall Islands. [/sup 239/Pu, /sup 240/Pu

    Energy Technology Data Exchange (ETDEWEB)

    Noshkin, V.E.; Eagle, R.J.; Wong, K.M.; Jokela, T.A.

    1980-09-01

    Concentrations of /sup 239 + 240/Pu are reported in tissues of several species of reef and pelagic fish caught at 14 different atolls in the northern Marshall Islands. Several regularities that are species dependent are evident in the distribution of /sup 239 + 240/Pu among different body tissues. Concentrations in liver always exceeded those in bone and concentrations were lowest in the muscle of all fish analyzed. A progressive discrimination against /sup 239 + 240/Pu was observed at successive trophic levels at all atolls except Bikini and Enewetak, where it was difficult to conclude if any real difference exists between the average concentration factor for /sup 239 + 240/Pu among all fish, which include bottom feeding and grazing herbivores, bottom feeding carnivores, and pelagic carnivores from different atoll locations. The average concentration of /sup 239 + 240/Pu in the muscle of surgeonfish from Bikini and Enewetak was not significantly different from the average concentrations determined in these fish at the other, lesser contaminated atolls. Concentrations among all 3rd, 4th, and 5th trophic level species are highest at Bikini where higher environmental concentrations are found. The reasons for the anomalously low concentrations in herbivores from Bikini and Enewetak are not known.

  18. Pu236(n,f), Pu237(n,f), and Pu238(n,f) cross sections deduced from (p,t), (p,d), and (p,p') surrogate reactions

    Science.gov (United States)

    Hughes, R. O.; Beausang, C. W.; Ross, T. J.; Burke, J. T.; Casperson, R. J.; Cooper, N.; Escher, J. E.; Gell, K.; Good, E.; Humby, P.; McCleskey, M.; Saastimoinen, A.; Tarlow, T. D.; Thompson, I. J.

    2014-07-01

    The Pu236(n,f), Pu237(n,f) and Pu238(n,f) cross sections have been inferred by utilizing the surrogate ratio method. Targets of Pu239 and U235 were bombarded with 28.5-MeV protons, and the light ion recoils, as well as fission fragments, were detected using the STARS detector array at the K150 Cyclotron at the Texas A&M cyclotron facility. The (p, tf) reaction on Pu239 and U235 targets was used to deduce the σ (Pu236(n ,f))/σ(U232(n,f)) ratio, and the Pu236(n,f) cross section was subsequently determined for En=0.5-7.5 MeV. Similarly, the (p,df) reaction on the same two targets was used to deduce the σ(Pu237(n ,f))/σ(U233(n,f)) ratio, and the Pu237(n,f) cross section was extracted in the energy range En=0.5-7 MeV. The Pu238(n,f) cross section was also deduced by utilizing the (p,p') reaction channel on the same targets. There is good agreement with the recent ENDF/B-VII.1 evaluated cross section data for Pu238(n,f) in the range En=0.5-10.5 MeV and for Pu237(n,f) in the range En=0.5-7 MeV; however, the Pu236(n,f) cross section deduced in the present work is higher than the evaluation between 2 and 7 MeV.

  19. Economical Production of Pu-238: NIAC Phase I Final Report

    Science.gov (United States)

    Howe, Steven D.; Crawford, Douglas; Navarro, Jorge; O'Brien, Robert C.; Katalenich, Jeff; Ring, Terry

    2016-01-01

    All space exploration missions traveling beyond Jupiter must use radioisotopic power sources for electrical power. The best isotope to power these sources is plutonium-238 (Pu-238). The US supply of Pu-238 is almost exhausted and will be gone within the next decade. The Department of Energy has initiated a production program with a $10M allocation from NASA but the cost is estimated at over $100M to get to production levels. The Center for Space Nuclear Research (CSNR) has conceived of a potentially better process to produce Pu-238 earlier and for significantly less cost. Potentially, the front end capital costs could be provided by private industry such that the government only had to pay for the product produced. In the Phase I NIAC (NASA Innovative Advanced Concepts) grant, the CSNR has evaluated the feasibility of using a low power, commercially available nuclear reactor to produce 1.5 kg of Pu-238 per year. The impact on the neutronics of the reactor have been assessed, the amount of Neptunium target material estimated, and the production rates calculated. In addition, the size of the post-irradiation processing facility has been established. Finally, as the study progressed, a new method for fabricating the Pu-238 product into the form used for power sources has been identified to reduce the cost of the final product. In short, the concept appears to be viable, can produce the amount of Pu-238 needed to support the NASA missions, can be available within a few years, and will cost significantly less than the current DOE program.

  20. Monte Carlo simulations of the stability of delta-Pu

    DEFF Research Database (Denmark)

    Landa, A.; Soderlind, P.; Ruban, Andrei

    2003-01-01

    The transition temperature (T-c) for delta-Pu has been calculated for the first time. A Monte Carlo method is employed for this purpose and the effective cluster interactions are obtained from first-principles calculations incorporated with the Connolly-Williams and generalized perturbation methods....... It is found that at T-c similar to 548 K, delta-Pu undergoes transformation from a disordered magnetic state to a structure with an anti ferromagnetic spin alignment that is mechanically unstable with respect to tetragonal distortion. The calculated transition temperature is in good agreement...

  1. Monte Carlo simulations of the stability of delta-Pu

    CERN Document Server

    Landa, A; Ruban, A

    2003-01-01

    The transition temperature (T sub c) for delta-Pu has been calculated for the first time. A Monte Carlo method is employed for this purpose and the effective cluster interactions are obtained from first-principles calculations incorporated with the Connolly-Williams and generalized perturbation methods. It is found that at T sub c approx 548 K, delta-Pu undergoes transformation from a disordered magnetic state to a structure with an antiferromagnetic spin alignment that is mechanically unstable with respect to tetragonal distortion. The calculated transition temperature is in good agreement with the temperature measured at the gamma -> delta transition (593 K). (letter to the editor)

  2. FY12 Final Report for PL10-Mod Separations-PD12: Electrochemically Modulated Separation of Plutonium from Dilute and Concentrated Dissolver Solutions for Analysis by Gamma Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Pratt, Sandra H.; Arrigo, Leah M.; Duckworth, Douglas C.; Cloutier, Janet M.; Breshears, Andrew T.; Schwantes, Jon M.

    2013-05-01

    Accurate and timely analysis of plutonium in spent nuclear fuel is critical in nuclear safeguards for detection of both protracted and rapid plutonium diversions. Gamma spectroscopy is a viable method for accurate and timely measurements of plutonium provided that the plutonium is well separated from the interfering fission and activation products present in spent nuclear fuel. Electrochemically modulated separation (EMS) is a method that has been used successfully to isolate picogram amounts of Pu from nitric acid matrices. With EMS, Pu adsorption may be turned “on” and “off” depending on the applied voltage, allowing for collection and stripping of Pu without the addition of chemical reagents. In this work, we have scaled up the EMS process to isolate microgram quantities of Pu from matrices encountered in spent nuclear fuel during reprocessing. Several challenges have been addressed including surface area limitations, radiolysis effects, electrochemical cell performance stability, and chemical interferences. After these challenges were resolved, 6 µg Pu was deposited in the electrochemical cell with approximately an 800-fold reduction of fission and activation product levels from a spent nuclear fuel sample. Modeling showed that these levels of Pu collection and interference reduction may not be sufficient for Pu detection by gamma spectroscopy. The main remaining challenges are to achieve a more complete Pu isolation and to deposit larger quantities of Pu for successful gamma analysis of Pu. If gamma analyses of Pu are successful, EMS will allow for accurate and timely on-site analysis for enhanced Pu safeguards.

  3. Space and Time Distribution of Pu Isotopes inside The First Experimental Fuel Pin Designed for PWR and Manufactured in Indonesia

    Science.gov (United States)

    Suwardi; Setiawan, J.; Susilo, J.

    2017-01-01

    The first short fuel pin containing natural UO2 pellet in Zry4 cladding has been prepared and planned to be tested in power ramp irradiation. An irradiation test should be designed to allow an experiment can be performed safely and giving maximum results of many performance aspects of design and manufacturing. Performance analysis to the fuel specimen shows that the specimen is not match to be used for power ramp testing. Enlargement by 0.20 mm of pellet diameter has been proposed. The present work is evaluation of modified design for important aspect of isotopic Pu distribution during irradiation test, because generated Pu isotopes in natural UO2 fuel, contribute more power relative to the contribution by enriched UO2 fuel. The axial profile of neutrons flux have been chosen from both experimental measurement and model calculation. The parameters of ramp power has been obtained from statistical experiment data. A simplified and typical base-load commercial PHWR profile of LHR history has been chosen, to determine the minimum irradiation time before ramp test can be performed. The data design and Mat pro XI materials properties models have been chosen. The axial profile of neutrons flux has been accommodated by 5 slices of discrete pin. The Pu distribution of slice-4 with highest power rate has been chosen to be evaluated. The radial discretion of pellet and cladding and numerical parameter have been used the default best practice of TU. The results shows that Pu 239 increased rapidly. The maximum burn up of slice 4 at upper the median slice, it reached nearly 90% of maximum value at about 6000 h with peak of 0.8%a Pu/HM at 22000 h, which is higher than initial U 235. Each 240, 241 and 240 Pu grows slower and ends up to 0.4, 0.2 and 0.18 % respectively. This results can be used for verification of other aspect of fuel behavior in the modeling results and also can be used as guide and comparison to the future post irradiation examination for Pu isotopes distribution.

  4. Measurement of the fission cross-section of $^{240}$Pu and $^{242}$Pu at CERN's n_TOF Facility

    CERN Multimedia

    Pavlik, A F; Gonzalez romero, E M

    The n_TOF Collaboration proposes to continue the fission program, already started in 2002-2004, taking advantage of the newly constructed Work Sector Type A, with the measurement of the two isotopes : $^{240}$ Pu and $^{242}$ Pu. They are both of major importance for reactor physics applications and are included in the Nuclear Energy Agency (NEA) High Priority List [1], in the NEA WPEC Subgroup 26 Report on the accuracy of nuclear data for advanced reactor designe [2] and in the EU 6$^{th}$ Framework Programme IP-EUROTRANS/NUDATRA reports [3]. Based on those requests, the measurement of the fission cross-section of the two Pu isotopes is one of the objectives of the project ANDES of the FP7 EURATOM program [4].

  5. Biogeochemical Cycling and Environmental Stability of Pu Relevant to Long-Term Stewardship of DOE Sites

    Energy Technology Data Exchange (ETDEWEB)

    Honeyman, Bruce D.; Francis, A.J.; Gillow, Jeffrey B.; Dodge, Cleveland J.; Santschi, Peter H.; Chin-Chang Hung; Diaz, Angelique; Tinnacher, Ruth; Roberts, Kimberly; Schwehr, Kathy

    2006-04-05

    The overall objective of this research is to understand the biogeochemical cycling of Pu in environments of interest to long-term DOE stewardship issues. Central to Pu cycling (transport initiation and immobilization) is the role of microorganisms. The hypothesis underlying this work is that microbial activity is the causative agent in initiating the mobilization of Pu in near-surface environments: through the transformation of Pu associated with solid phases, production of extracellular polymeric substances (EPS) carrier phases and the creation of microenvironments. Also, microbial processes are central to the immobilization of Pu species, through the metabolism of organically complexed Pu species and Pu associated with extracellular carrier phases and the creation of environments favorable for Pu transport retardation.

  6. Biogeochemical Cycling and Environmental Stability of Pu Relevant to Long-Term Stewardship of DOE Sites

    Energy Technology Data Exchange (ETDEWEB)

    Francis, Arokiasamy J.; Santschi, Peter H.; Honeyman, Bruce D.

    2005-06-01

    The overall objective of this proposed research is to understand the biogeochemical cycling of Pu in environments of interest to long-term DOE stewardship issues. Central to Pu cycling (transport initiation to immobilization) is the role of microorganisms. The hypothesis underlying this proposal is that microbial activity is the causative agent in initiating the mobilization of Pu in near-surface environments: through the transformation of Pu associated with solid phases, production of extracellular polymeric substances (EPS) carrier phases, and the creation of microenvironments. Also, microbial processes are central to the immobilization of Pu species, through the metabolism of organically complexed Pu species and Pu associated with extracellular carrier phases and the creation of environments favorable for Pu transport retardation.

  7. Recovery of Pu,Np in 1BP of Dilute TBP Extraction Process

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    <正>In the TBP extraction process, Np and Pu need to be recovered from effluents of the TBP extraction process. In this work, the recovery of Np and Pu from TBP extraction effluents is studied was investigated

  8. Temporal record of Pu isotopes in inter-tidal sediments from the northeastern Irish Sea

    Energy Technology Data Exchange (ETDEWEB)

    Lindahl, Patric, E-mail: patriclindahl@yahoo.com [School of Geography, Earth and Environmental Sciences, University of Plymouth, Drake Circus, Plymouth PL4 8AA (United Kingdom); Worsfold, Paul; Keith-Roach, Miranda [School of Geography, Earth and Environmental Sciences, University of Plymouth, Drake Circus, Plymouth PL4 8AA (United Kingdom); Andersen, Morten B. [Bristol Isotope Group, School of Earth Sciences, University of Bristol, Wills Memorial Building, Bristol BS8 1RJ (United Kingdom); Kershaw, Peter; Leonard, Kins [The Centre for Environment, Fisheries and Aquaculture Science, Lowestoft Laboratory, Pakefield Road, Suffolk NR33 0HT (United Kingdom); Choi, Min-Seok [Division of Earth and Environmental Science, Korea Basic Science Institute, 113 Gwahangno, Yusung-gu, Daejon 305-333 (Korea, Republic of); Boust, Dominique [Laboratoire de Radioecologie, Institut de Radioprotection et de Surete Nucleaire, BP 10, 50130 Cherbourg-Octeville (France); Lesueur, Patrick [University of Caen Basse Normandie, M2C UMR CNRS 6143, 14000 Caen (France)

    2011-11-01

    A depth profile of {sup 239}Pu and {sup 240}Pu specific activities and isotope ratios was determined in an inter-tidal sediment core from the Esk Estuary in the northeastern Irish Sea. The study site has been impacted with plutonium through routine radionuclide discharges from the Sellafield nuclear reprocessing plant in Cumbria, NW England. A pronounced sub-surface maximum of {approx} 10 kBq kg{sup -1} was observed for {sup 239+240}Pu, corresponding to the peak in Pu discharge from Sellafield in 1973, with a decreasing trend with depth down to {approx} 0.04 kBq kg{sup -1} in the deeper layers. The depth profile of {sup 239+240}Pu specific activities together with results from gamma-ray spectrometry for {sup 137}Cs and {sup 241}Am was compared with reported releases from the Sellafield plant in order to estimate a reliable sediment chronology. The upper layers (1992 onwards) showed higher {sup 239+240}Pu specific activities than would be expected from the direct input of annual Sellafield discharges, indicating that the main input of Pu is from the time-integrated contaminated mud patch of the northeastern Irish Sea. The {sup 240}Pu/{sup 239}Pu atom ratios ranged from {approx} 0.03 in the deepest layers to > 0.20 in the sub-surface layers with an activity-weighted average of 0.181. The decreasing {sup 240}Pu/{sup 239}Pu atom ratio with depth reflects the changing nature of operations at the Sellafield plant from weapons-grade Pu production to reprocessing spent nuclear fuel with higher burn-up times in the late 1950s. In addition, recent annual {sup 240}Pu/{sup 239}Pu atom ratios in winkles collected during 2003-2008 from three stations along the Cumbrian coastline showed no significant spatial or temporal differences with an overall average of 0.204, which supports the hypothesis of diluted Pu input from the contaminated mud patch. - Highlights: {yields} Depth profiles of {sup 239}Pu and {sup 240}Pu determined in a northeastern Irish Sea sediment. {yields

  9. Study of the Effect of (U0.8Pu0.2O2 Uranium–Plutonium Mixed Fuel Fission Products on a Living Organism

    Directory of Open Access Journals (Sweden)

    Ayagoz Baimukhanova

    2016-08-01

    Full Text Available The article describes the results of experiments conducted on pigs to determine the effect of plutonium, which is the most radiotoxic and highly active element in the range of mixed fuel (U0.8Pu0.2O2 fission products, on living organisms. The results will allow empirical prediction of the emergency plutonium radiation dose for various organs and tissues of humans in case of an accident in a reactor running on mixed fuel (U0.8Pu0.2O2.

  10. Control of Urania Crystallite Size by HMTA-Urea Reactions in the Internal Gelation Process for Preparing (U, Pu)O2Fuel Kernels

    Energy Technology Data Exchange (ETDEWEB)

    Collins, J.L.

    2005-04-26

    In the development of (U,Pu)O{sub 2} kernels by the internal gelation process for the Direct Press Spheroidized process at Oak Ridge National Laboratory, a novel crystal growth step was discovered that made it possible to prepare calcined porous kernels that could be used as direct-press feed for Fast Breeder Reactor pellet fabrication. High-quality pellets were prepared that were near theoretical density and that (upon examination) revealed no evidence of sphere remnants. The controlled crystal growth step involved using hexamethylenetetramine (HMTA)-urea stock solutions that were boiled for 60 min or less. Before this discovery, all the other crystal growth steps (when utilized) could reduce the tap density to only {approx}1.3 g/cm{sup 3}, which was not sufficiently low for use in ideal pellet pressing. The use of the boiled HMTA-urea solution allowed the tap density to be lowered to 0.93 g/cm{sup 3}, with the ideal density being about 1.0 g/cm{sup 3}. This report describes the development of this technology and its scaleup.

  11. Atomic Structure and Phase Transformations in Pu Alloys

    Energy Technology Data Exchange (ETDEWEB)

    Schwartz, A J; Cynn, H; Blobaum, K M; Wall, M A; Moore, K T; Evans, W J; Farber, D L; Jeffries, J R; Massalski, T B

    2008-04-28

    Plutonium and plutonium-based alloys containing Al or Ga exhibit numerous phases with crystal structures ranging from simple monoclinic to face-centered cubic. Only recently, however, has there been increased convergence in the actinides community on the details of the equilibrium form of the phase diagrams. Practically speaking, while the phase diagrams that represent the stability of the fcc {delta}-phase field at room temperature are generally applicable, it is also recognized that Pu and its alloys are never truly in thermodynamic equilibrium because of self-irradiation effects, primarily from the alpha decay of Pu isotopes. This article covers past and current research on several properties of Pu and Pu-(Al or Ga) alloys and their connections to the crystal structure and the microstructure. We review the consequences of radioactive decay, the recent advances in understanding the electronic structure, the current research on phase transformations and their relations to phase diagrams and phase stability, the nature of the isothermal martensitic {delta} {yields} {alpha}{prime} transformation, and the pressure-induced transformations in the {delta}-phase alloys. New data are also presented on the structures and phase transformations observed in these materials following the application of pressure, including the formation of transition phases.

  12. DIRAC: a community grid solution

    CERN Document Server

    Tsaregorodtsev, A; Brook, N; Ramo, A C; Castellani, G; Charpentier, P; Cioffi, C; Closier, J; Díaz, R G; Kuznetsov, G; Li, Y Y; Nandakumar, R; Paterson, S; Santinelli, R; Smith, A C; Miguelez, M S; Jimenez, S G

    2008-01-01

    The DIRAC system was developed in order to provide a complete solution for using the distributed computing resources of the LHCb experiment at CERN for data production and analysis. It allows a concurrent use of over 10K CPUs and 10M file replicas distributed over many tens of sites. The sites can be part of a Computing Grid such as WLCG or standalone computing clusters all integrated in a single management structure. DIRAC is a generic system with the LHCb specific functionality incorporated through a number of plug-in modules. It can be easily adapted to the needs of other communities. Special attention is paid to the resilience of the DIRAC components to allow an efficient use of non-reliable resources. The DIRAC production management components provide a framework for building highly automated data production systems including data distribution and data driven workload scheduling. In this paper we give an overview of the DIRAC system architecture and design choices. We show how different components are pu...

  13. Transuranic advanced disposal systems: preliminary /sup 239/Pu waste-disposal criteria for Hanford

    Energy Technology Data Exchange (ETDEWEB)

    Kennedy, W.E. Jr.; Aaberg, R.L.; Napier, B.A.; Soldat, J.K.

    1982-09-01

    This report contains the draft results of a study sponsored by the US Department of Energy (DOE) to determine preliminary /sup 239/Pu waste disposal criteria for the Hanford Site. The purpose of this study is to provide a preliminary evaluation of the feasibility of various defense TRU advanced disposal options at the Hanford Site. Advanced waste disposal options include those developed to provide greater confinement than provided by shallow-land burial. They will be used to complement the waste geologic disposal in achieving permanent disposal of selected TRU wastes. An example systems analysis is discussed with assumed performance objectives and Hanford-specific disposal conditions, waste forms, site characteristics, and engineered barriers. Preliminary waste disposal criteria for /sup 239/Pu are determined by applying the Allowable Residual Contamination Level (ARCL) method. This method is based on compliance with a radiation dose rate limit through a site-specific analysis of the potential for radiation exposure to individuals. A 10,000-year environmental performance period is assumed, and the dose rate limit for human intrusion is assumed to be 500 mrem/yr to any exposed individual. Preliminary waste disposal criteria derived by this method for /sup 239/Pu in soils at the Hanford Site are: 0.5 nCi/g in soils between the surface and a depth of 1 m, 2200 nCi/g of soil at a depth of 5 m, and 10,000 nCi/g of soil at depths 10 m and below. These waste disposal criteria are based on exposure scenarios that reflect the dependence of exposure versus burial depth. 5 figures, 7 tables.

  14. Molecular analysis of the interaction between the hematopoietic master transcription factors GATA-1 and PU.1

    DEFF Research Database (Denmark)

    Liew, Chu Wai; Rand, Kasper Dyrberg; Simpson, Raina J Y

    2006-01-01

    GATA-1 and PU.1 are transcription factors that control erythroid and myeloid development, respectively. The two proteins have been shown to function in an antagonistic fashion, with GATA-1 repressing PU.1 activity during erythropoiesis and PU.1 repressing GATA-1 function during myelopoiesis. It h...

  15. Preliminary Study on the Determination of ~(235)U and ~(239)Pu Using Delayed Neutron Counting Method

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    The preliminary study on the fast measurements of 235U and 239Pu in samples containing 235U, 239Pu and 235U-239Pu mixture using delayed neutron counting method is introduced. All samples were irradiated for 30 s using the 30 kW Miniature Neutron

  16. Symbiotic Pu/Th fuel cycle for HTGR

    Energy Technology Data Exchange (ETDEWEB)

    Girardi, Enrico; Lecarpentier, David [EDF R and D, Les Renardieres, 77818 Moret sur Loing cedex (France)

    2006-07-01

    HTGRs, loaded with uranium or plutonium fuel do not authorize high breeding ratios. Consequently, the Gen IV requirement of sustainability with respect to the use of fissile resources may be difficult to meet. Relying on the thorium conversion into fissile uranium 233, the use of thorium is promising regarding the breeding ratio. Accordingly, the symbiotic Pu/Th fuel cycle is an interesting way to optimize the energetic use of plutonium. In the first part of this paper, we compare the performances of HTRs with different types of fuel (15% enriched U, Pu alone, Th-Pu) on the resource consumption. Relying on HTGRs, a good conversion ratio (typically 0.8) is mandatory to satisfy high temperature needs in the long term. In the second part, we discuss the neutronic calculation scheme for a prismatic HTGR annular core (GTMHR like, with an internal graphite reflector), and for a large HTGR (modeled with an assembly calculation). In the last part of the paper, Pu/Th, U233/Th and Pu-U233/Th fuel cycle are studied for the two types of HTGRs. The performances in terms of conversion ratios are compared. For a given power of 300 Mwe, several compositions for the fuel are studied. The fraction of thorium in the fuel composition is varying from 0% to 99% and the total fuel mass charged in the core ranges from 1200 kg to 15,000 kg. We show that good conversion ratios are very difficult to obtain for annular HTGRs. New designs must be considered, with a larger core, and a smaller power density (to reach the passive evacuation of residual power). Finally, a preliminary strategy for the deployment of these fuel cycles is presented. (authors)

  17. A theoretical study of the ground state and lowest excited states of PuO0/+/+2 and PuO20/+/+2

    Energy Technology Data Exchange (ETDEWEB)

    Gibson, John K.; La Macchia, Giovanni; Infante, Ivan; Gagliardi, Laura; Raab, Juraj

    2008-12-08

    The ground and excited states of neutral and cationic PuO and PuO2 have been studied with multiconfigurational quantum chemical methods followed by second order perturbation theory, the CASSCF/CASPT2 method. Scalar relativistic effects and spin-orbit coupling have been included in the treatment. As literature values for the ionization energy of PuO2 are in the wide range of ~;;6.6 eV to ~;;10.1 eV, a central goal of the computations was to resolve these discrepancies; the theoretical results indicate that the ionization energy is near the lower end of this range. The calculated ionization energies for PuO, PuO+ and PuO2+ are in good agreement with the experimental values.

  18. (137)Cs, (239+240)Pu concentrations and the (240)Pu/(239)Pu atom ratio in a sediment core from the sub-aqueous delta of Yangtze River estuary.

    Science.gov (United States)

    Pan, S M; Tims, S G; Liu, X Y; Fifield, L K

    2011-10-01

    A sediment core collected from the sub-aqueous delta of the Yangtze River estuary was subjected to analyses of (137)Cs and plutonium (Pu) isotopes. The (137)Cs was measured using γ-spectrometry at the laboratories at the Nanjing University and Pu isotopes were determined with Accelerator Mass Spectrometry (AMS), measurements made at the Australian National University. The results show considerable structure in the depth concentration profiles of the (137)Cs and (239+240)Pu. The shape of the vertical (137)Cs distribution in the sediment core was similar to that of the Pu. The maximum (137)Cs and (239+240)Pu concentrations were 16.21 ± 0.95 mBq/g and 0.716 ± 0.030 mBq/g, respectively, and appear at same depth. The average (240)Pu/(239)Pu atom ratio was 0.238 ± 0.007 in the sediment core, slightly higher than the average global fallout value. The changes in the (240)Pu/(239)Pu atom ratios in the sediment core indicate the presence of at least two different Pu sources, i.e., global fallout and another source, most likely close-in fallout from the Pacific Proving Grounds (PPG) in the Marshall Islands, and suggest the possibility that Pu isotopes are useful as a geochronological tool for coastal sediment studies. The (137)Cs and (239+240)Pu inventories were estimated to be 7100 ± 1200 Bq/m(2) and 407 ± 27 Bq/m(2), respectively. Approximately 40% of the (239+240)Pu inventory originated from the PPG close-in fallout and about 50% has derived from land-origin global fallout transported to the estuary by the river. This study confirms that AMS is a useful tool to measure (240)Pu/(239)Pu atom ratio and can provide valuable information on sedimentary processes in the coastal environment.

  19. Identification of Nilsson orbitals in the superdeformed minimum of {sup 237}Pu

    Energy Technology Data Exchange (ETDEWEB)

    Morgan, Thomas James

    2008-03-31

    -particle calculations, Nilsson model and Woods-Saxon potential calculations. This comparison allowed for the first time an assignment of the Nilsson quantum numbers. In the course of this thesis the 5/2{sup +}[862] and 9/2{sup +}[624] Nilsson single-particle states were identified for the ground states of the two isomers in {sup 237f}Pu as well as 3/2{sup -}[512] and 7/2{sup -}[514] for excited rotational bands, for the first time based on calculations reproducing the deformed magic neutron number N=146. The identification of Nilsson orbitals will provide an important input for the validation and improvement of theoretical nuclear models and will lead to improved predictions for fission barriers and their extrapolations to neutron-rich heavy elements in the mass region of the r-process path of the astrophysical nucleosynthesis. (orig.)

  20. Variations in Pu isotopic composition in soils from the Spitsbergen (Norway): Three potential pollution sources of the Arctic region.

    Science.gov (United States)

    Łokas, E; Anczkiewicz, R; Kierepko, R; Mietelski, J W

    2017-07-01

    Although the polar regions have not been industrialised, numerous contaminants originating from human activity are detectable in the Arctic environment. This study reports evidence of (240)Pu/(239)Pu atomic ratios in the tundra and initial soils from different parts of west and central Spitsbergen and recognizes possible environmental inputs of non-global fallout Pu. The average atomic ratio of (240)Pu/(239)Pu equal to 0.179 (ranging between 0.129 and 0.201) in tundra soils are comparable to the characteristic ratio for global fallout (0.180). However, the (240)Pu/(239)Pu atomic ratios in the initial soils from proglacial zone of glaciers change within wide range between 0.1281 and 0.234 with the mean value of 0.169. By combining alpha and mass spectrometry, the three-sources model was used to identify the Pu sources in initial soils. Our study indicated that the main source of Pu is nuclear tests and that a second source with lower Pu ratio may come from weapons grade Pu (unexploded weapons grade Pu ie. material from bomb which didn't undergo nuclear explosions for example for security tests). Additionally, we found samples with high (238)Pu/(239+240)Pu activity ratios and with typical global fallout (240)Pu/(239)Pu atomic ratios, which are associated with separate sources of pure (238)Pu from the SNAP-9A satellite burn up in the atmosphere. Copyright © 2017 Elsevier Ltd. All rights reserved.

  1. Release of Pu isotopes from the Fukushima Daiichi Nuclear Power Plant accident to the marine environment was negligible.

    Science.gov (United States)

    Bu, Wenting; Fukuda, Miho; Zheng, Jian; Aono, Tatsuo; Ishimaru, Takashi; Kanda, Jota; Yang, Guosheng; Tagami, Keiko; Uchida, Shigeo; Guo, Qiuju; Yamada, Masatoshi

    2014-08-19

    Atmospheric deposition of Pu isotopes from the Fukushima Daiichi Nuclear Power Plant (FDNPP) accident has been observed in the terrestrial environment around the FDNPP site; however, their deposition in the marine environment has not been studied. The possible contamination of Pu in the marine environment has attracted great scientific and public concern. To fully understand this possible contamination of Pu isotopes from the FDNPP accident to the marine environment, we collected marine sediment core samples within the 30 km zone around the FDNPP site in the western North Pacific about two years after the accident. Pu isotopes ((239)Pu, (240)Pu, and (241)Pu) and radiocesium isotopes ((134)Cs and (137)Cs) in the samples were determined. The high activities of radiocesium and the (134)Cs/(137)Cs activity ratios with values around 1 (decay corrected to 15 March 2011) suggested that these samples were contaminated by the FDNPP accident-released radionuclides. However, the activities of (239+240)Pu and (241)Pu were low compared with the background level before the FDNPP accident. The Pu atom ratios ((240)Pu/(239)Pu and (241)Pu/(239)Pu) suggested that global fallout and the pacific proving ground (PPG) close-in fallout are the main sources for Pu contamination in the marine sediments. As Pu isotopes are particle-reactive and they can be easily incorporated with the marine sediments, we concluded that the release of Pu isotopes from the FDNPP accident to the marine environment was negligible.

  2. Binding of Pu(IV) to galacturonic acid and extracellular polymeric substances (EPS) from Shewanella putrefaciens, Clostridium sp. and Pseudomonas fluorescens

    Energy Technology Data Exchange (ETDEWEB)

    Harper, R.M. [Dept. of Environmental Sciences, Huxley Coll. of the Environment, Western Washington Univ., WA (United States); Kantar, C. [Dept. of Environmental Engineering, Mersin Univ., Ciftllikkoy, Mersin (Turkey); Honeyman, B.D. [Environmental Science and Engineering Div., Colorado School of Mines, Golden, CO (United States)

    2008-07-01

    The conditional stability constants for trace-level concentrations of Pu(IV) complexing with galacturonic acid and EPS, isolated from axenic Clostridium sp., P. fluorescens and Shewanella putrefaciens CN32 cultures, were determined at pH 4 and an ionic strength of 0.1 M NaCl using an ion-exchange technique. The analysis of ion-exchange data with Schubert's technique indicates that the Pu binding by galacturonic acid and EPS from Clostridium sp. and S. putrefaciens can be described based on the formation of 1: 1 Pu(IV)-ligand complexes. However, the accurate description of Pu binding by EPS from P. fluorescens requires postulation of a mixture of 1: 1/1: 2 complexes between Pu(IV) and ligands under the experimental conditions studied. The results from the ion-exchange experiments were also modeled based on a non-electrostatic, discrete ligand approach in which bacterial EPS is conceptualized as being composed of a suite of monoprotic acids, HL{sub 1}, of arbitrarily-assigned pK{sub a} (i) values (e.g., 4, 6 and 8). The examination of ion-exchange data in a chemical model suggested that only the pK{sub a} 4 (L{sub 1}) and 6 (L{sub 2}) ligands are sufficient to accurately simulate the Pu(IV)/EPS binding, implying that carboxylic groups in EPS are the primary binding sites for complexing with Pu(IV) under the experimental conditions examined. The affinity of EPS for complexing Pu(IV) decreases in the order of Clostridium sp. > S. putrefaciens > P. fluorescens although the concentrations of carboxylic groups in EPS decrease in the order of P. fluorescens > S. putrefaciens > Clostridium sp. This discrepancy may be due to differences in binding affinities between Na{sup +} ion in solution and EPS ligands. At I = 0.1 M, models demonstrated that the EPS from P. fluorescens exhibits a much stronger affinity for the Na{sup +} ion compared to ligands from other EPS; therefore, the deprotonated carboxylic sites of EPS from P. fluorescens are hypothesized to be mostly bound

  3. Transport process of Pu isotope in marginal seas of the western North Pacific Ocean

    Energy Technology Data Exchange (ETDEWEB)

    Yamada, Masatoshi [Department of Radiation Chemistry, Institute of Radiation Emergency Medicine, Hirosaki University, Hirosaki, 036-8564, Aomori (Japan); Zheng, Jian [Research Center for Radiation Protection, National Institute of Radiological Sciences, 4-9-1 Anagawa, Inage, 263-8555, Chiba (Japan)

    2014-07-01

    Significant quantities of Pu isotopes have been released into the marine environment as the result of atmospheric nuclear weapons testing. Most radionuclides globally dispersed in atmospheric nuclear weapons testing were released into the environment during the 1950's and 1960's. In the western North Pacific Ocean, the principal source can be further distinguished as two distinct sources of Pu: close-in tropospheric fallout from nuclear weapons testing at the Pacific Proving Grounds (PPG) in the Marshall Islands and global stratospheric fallout. Since the {sup 240}Pu/{sup 239}Pu atom ratio is characteristic for the Pu emission source, information on Pu isotopic signature is very useful to better understand the transport process in the oceans and to identify the sources of Pu. The mean atom ratio of {sup 240}Pu/{sup 239}Pu from the global stratospheric fallout is 0.180 ±0.014 based on soil sample data, whereas that from close-in tropospheric fallout from the PPG is 0.33 - 0.36. The {sup 240}Pu/{sup 239}Pu atom ratios in seawater samples collected in marginal seas of the western North Pacific Ocean will provide important and useful data for understanding the process controlling Pu transport and for distinguishing future Pu sources. The objectives of this study were to measure the {sup 239+240}Pu concentrations and {sup 240}Pu/{sup 239}Pu atom ratios in seawater from the Sea of Okhotsk, Japan Sea, South China Sea and Sulu Sea and to discuss the transport process of Pu. Large-volume seawater samples (250 L each) were collected from the surface to the bottom in marginal seas of the western North Pacific Ocean with acoustically triggered quadruple PVC sampling bottles during the R/V Hakuho-Maru cruise. The {sup 239}Pu and {sup 240}Pu concentrations and {sup 240}Pu/{sup 239}Pu atom ratios were measured with a double-focusing SF-ICP-MS, which was equipped with a guard electrode to eliminate secondary discharge in the plasma and to enhance overall sensitivity. In

  4. AMS of natural 236U and 239Pu produced in uranium ores

    Science.gov (United States)

    Wilcken, K. M.; Barrows, T. T.; Fifield, L. K.; Tims, S. G.; Steier, P.

    2007-06-01

    The rare isotopes 236U and 239Pu are produced naturally by neutron capture in uranium ores. Here we measure 236U and 239Pu by accelerator mass spectrometry (AMS) in the same ore samples for the first time. To ensure efficient extraction of both elements and isotopic equilibrium between the 239Pu in the ore and a 242Pu spike, we developed a new sample preparation protocol. AMS has clear advantages over previous methods because it achieves better discrimination against molecular interferences with higher sensitivity and shorter counting times. Measurements of 236U and 239Pu hold considerable promise as proxy indicators of neutron flux and uranium concentration.

  5. Vertical distribution of (241)Pu in the southern Baltic Sea sediments.

    Science.gov (United States)

    Strumińska-Parulska, Dagmara I

    2014-12-15

    The vertical distribution of plutonium (241)Pu in marine sediments can assist in determining the deposition history and sedimentation process of analyzed regions. In addition, (241)Pu/(239+240)Pu activity ratio could be used as a sensitive fingerprint for radioactive source identification. The present preliminary studies on vertical distribution of (241)Pu in sediments from four regions of the southern Baltic Sea are presented. The distribution of (241)Pu was not uniform and depended on sediment geomorphology and depth as well as location. The highest concentrations of plutonium were found in the surface layers of all analyzed sediments and originated from the Chernobyl accident.

  6. Anaerobic Biotransformation and Mobility of Pu and of Pu-EDTA

    Energy Technology Data Exchange (ETDEWEB)

    Xun, Luying

    2009-11-20

    The enhanced mobility of radionuclides by co-disposed chelating agent, ethylenediaminetetraacetate (EDTA), is likely to occur only under anaerobic conditions. Our extensive effort to enrich and isolate anaerobic EDTA-degrading bacteria has failed. Others has tried and also failed. To explain the lack of anaerobic biodegradation of EDTA, we proposed that EDTA has to be transported into the cells for metabolism. A failure of uptake may contribute to the lack of EDTA degradation under anaerobic conditions. We demonstrated that an aerobic EDTA-degrading bacterium strain BNC1 uses an ABC-type transporter system to uptake EDTA. The system has a periplasmic binding protein that bind EDTA and then interacts with membrane proteins to transport EDTA into the cell at the expense of ATP. The bind protein EppA binds only free EDTA with a Kd of 25 nM. The low Kd value indicates high affinity. However, the Kd value of Ni-EDTA is 2.4 x 10^(-10) nM, indicating much stronger stability. Since Ni and other trace metals are essential for anaerobic respiration, we conclude that the added EDTA sequestrates all trace metals and making anaerobic respiration impossible. Thus, the data explain the lack of anaerobic enrichment cultures for EDTA degradation. Although we did not obtain an EDTA degrading culture under anaerobic conditions, our finding may promote the use of certain metals that forms more stable metal-EDTA complexes than Pu(III)-EDTA to prevent the enhanced mobility. Further, our data explain why EDTA is the most dominant organic pollutant in surface waters, due to the lack of degradation of certain metal-EDTA complexes.

  7. Analysis of Operating Strategies Using Different Target Designs For 238Pu Production

    Energy Technology Data Exchange (ETDEWEB)

    Thomas, Tomcy [University of Tennessee (UT); Sherman, Steven R [ORNL; Sawhney, Dr. Rapinder [University of Tennessee (UT)

    2017-01-01

    An engineering effort is underway to re-establish capability to produce 238Pu oxide at the kilogram scale in the United States. A multi-step batch process is being developed to produce this important material. Recently, a portion of this process was studied using discrete-event simulation tools to determine whether the conceptual process might achieve its yearly production goal. The study showed the conceptual process can meet the yearly production goal under some circumstances, but process improvements would be needed to ensure greater likelihood of success. This study extends the work performed previously by examining the effects of changing the reactor target design on the yearly process output. Two new reactor target configurations are considered an aluminum-clad reactor target containing 50% greater 237Np oxide content than the original target, and a zirconium alloy-clad target using no aluminum. The results indicate that use of the new aluminum-clad target configuration may allow the process to achieve the same yearly production goal in less time using fewer targets. If the zirconium alloy-clad target is used, then even fewer targets would be needed to reach the production goal, but some process changes would be required to handle the zirconium cladding. The number of days needed to process a target batch to completion, and the steady state 238Pu oxide production rate, for each configuration are compared to the results from the initial simulation study.

  8. Consistent Data Assimilation of Actinide Isotopes: 235U and 239Pu

    Energy Technology Data Exchange (ETDEWEB)

    G. Palmiottti; H. Hiruta; M. Salvatores

    2011-09-01

    In this annual report we illustrate the methodology of the consistent data assimilation that allows to use the information coming from integral experiments for improving the basic nuclear parameters used in cross section evaluation. A series of integral experiments were analyzed using the EMPIRE evaluated files for {sup 235}U, {sup 238}U, and {sup 239}Pu. Inmost cases the results have shown quite large worse results with respect to the corresponding existing evaluations available for ENDF/B-VII. The observed discrepancies between calculated and experimental results were used in conjunction with the computed sensitivity coefficients and covariance matrix for nuclear parameters in a consistent data assimilation. Only the GODIVA and JEZEBEL experimental results were used, in order to exploit information relative to the isotope of interest that are, in this particular case: {sup 235}U and {sup 239}Pu. The results obtained by the consistent data assimilation indicate that with reasonable modifications (mostly within the initial standard deviation) it is possible to eliminate the original large discrepancies on the K{sub eff} of the two critical configurations. However, some residual discrepancy remains for a few fission spectral indices that are, most likely, to be attributed to the detector cross sections.

  9. PuMaII: A wide band pulsar machine for the WSRT

    CERN Document Server

    Karuppusamy, Ramesh; van Straten, Willem

    2008-01-01

    The Pulsar Machine II (PuMa II) is the new flexible pulsar processing backend system at the Westerbork Synthesis Radio Telescope (WSRT), specifically designed to take advantage of the upgraded WSRT. The instrument is based on a computer cluster running the Linux operating system, with minimal custom hardware. A maximum of 160 MHz analogue bandwidth sampled as 8X20 MHz subbands with 8-bit resolution can be recorded on disks attached to separate computer nodes. Processing of the data is done in the additional 32-nodes allowing near real time coherent dedispersion for most pulsars observed at the WSRT. This has doubled the bandwidth for pulsar observations in general, and has enabled the use of coherent dedispersion over a bandwidth eight times larger than was previously possible at the WSRT. PuMa II is one of the widest bandwidth coherent dedispersion machines currently in use and has a maximum time resolution of 50ns. The system is now routinely used for high precision pulsar timing studies, polarization studi...

  10. Transuranic advanced disposal systems: preliminary /sup 239/Pu waste-disposal criteria for Hanford

    Energy Technology Data Exchange (ETDEWEB)

    Kennedy, W.E. Jr.; Napier, B.A.; Soldat, J.K.

    1982-08-01

    An evaluation of the feasibility and potential application of advanced disposal systems is being conducted for defense transuranic (TRU) wastes at the Hanford Site. The advanced waste disposal options include those developed to provide greater confinement than provided by shallow-land burial. An example systems analysis is discussed with assumed performance objectives and various Hanford-specific disposal conditions, waste forms, site characteristics, and engineered barriers. Preliminary waste disposal criteria for /sup 239/Pu are determined by applying the Allowable Residual Contamination Level (ARCL) method. This method is based on compliance with a radiation dose rate limit through a site-specific analysis of the potential for radiation exposure to individuals. A 10,000 year environmental performance period is assumed, and the dose rate limit for human intrusion is assumed to be 500 mrem/y to any exposed individual. Preliminary waste disposal criteria derived by this method for /sup 239/Pu in soils at the Hanford Site are: 0.5 nCi/g in soils between the surface and a depth of 1 m, 2200 nCi/g of soil at a depth of 5 m, and 10,000 nCi/g of soil at depths 10 m and below. These waste disposal criteria are based on exposure scenarios that reflect the dependence of exposure versus burial depth. 2 figures, 5 tables.

  11. PLUTONIUM SOLUBILITY IN SIMULATED SAVANNAH RIVER SITE WASTE SOLUTIONS

    Energy Technology Data Exchange (ETDEWEB)

    Rudisill, T.; Hobbs, D.; Edwards, T.

    2010-09-27

    To address the accelerated disposition of the supernate and salt portions of Savannah River Site (SRS) high level waste (HLW), solubility experiments were performed to develop a predictive capability for plutonium (Pu) solubility. A statistically designed experiment was used to measure the solubility of Pu in simulated solutions with salt concentrations and temperatures which bounded those observed in SRS HLW solutions. Constituents of the simulated waste solutions included: hydroxide (OH{sup -}), aluminate (Al(OH){sub 4}{sup -}), sulfate (SO{sub 4}{sup 2-}), carbonate (CO{sub 3}{sup 2-}), nitrate (NO{sub 3}{sup -}), and nitrite (NO{sub 2}{sup -}) anions. Each anion was added to the waste solution in the sodium form. The solubilities were measured at 25 and 80 C. Five sets of samples were analyzed over a six month period and a partial sample set was analyzed after nominally fifteen months of equilibration. No discernable time dependence of the measured Pu concentrations was observed except for two salt solutions equilibrated at 80 C which contained OH{sup -} concentrations >5 mol/L. In these solutions, the Pu solubility increased with time. This observation was attributed to the air oxidation of a portion of the Pu from Pu(IV) to the more soluble Pu(V) or Pu(VI) valence states. A data driven approach was subsequently used to develop a modified response surface model for Pu solubility. Solubility data from this study and historical data from the literature were used to fit the model. The model predicted the Pu solubility of the solutions from this study within the 95% confidence interval for individual predictions and the analysis of variance indicated no statistically significant lack of fit. The Savannah River National Laboratory (SRNL) model was compared with predicted values from the Aqueous Electrolyte (AQ) model developed by OLI Systems, Inc. and a solubility prediction equation developed by Delegard and Gallagher for Hanford tank waste. The agreement between

  12. Studies on Caffeine Content in Pu-Er Crude Tea and Pu-Er Ripe Tea%普洱生茶和熟茶中咖啡因含量测试

    Institute of Scientific and Technical Information of China (English)

    陈靖; 邹艳丽; 李聪; 王波; 谢启明

    2012-01-01

    Caffein was respectively extracted from 15 kinds of Pu-Er crude tea and 15 kinds of ripe tea by the boiling-water method.The caffein content was respectively determined by the ultraviolet spectrophotometric method,taken caffein as reference standard and the distilled water as the blank control,the absorbance of the reference and test solution was determined at 274 nm and the content of caffein was calculated by using the standard curve.The regression equation was y=47.945x+0.0015,R2=0.9999(Y and X stand for absorbance and concentration of caffein respectively),the average percentage composition of caffeine in Pu-Er crude tea was 4.29%,3.31% in Pu-Er ripe tea.The caffeine content of Pu-Er ripe tea is reduced during manufacturing process.%用热水浸提法分别提取15个普洱生茶样品和15个普洱熟茶样品中的咖啡因,采用紫外分光光度法,以咖啡因为标准品,蒸馏水为空白对照,于274 nm波长处分别测定对照品和供试品溶液的吸光度,按标准曲线计算咖啡因含量。回归方程为y=47.945x+0.0015,R2=0.9999。15个普洱生茶样品中的咖啡因平均含量4.29%,15个普洱熟茶样品中咖啡因平均含量为3.31%。

  13. 238Pu: accumulation, tissue distribution, and excretion in Mayak workers after exposure to plutonium aerosols.

    Science.gov (United States)

    Suslova, Klara G; Sokolova, Alexandra B; Khokhryakov, Viktor V; Miller, Scott C

    2012-03-01

    The alpha spectrometry measurements of specific activity of 238Pu and 239Pu in urine from bioassay examinations of 1,013 workers employed at the radiochemical and plutonium production facilities of the Mayak Production Association and in autopsy specimens of lung, liver, and skeleton from 85 former nuclear workers who died between 1974-2009, are summarized.The accumulation fraction of 238Pu in the body and excreta has not changed with time in workers involved in production of weapons-grade plutonium production (e.g., the plutonium production facility and the former radiochemical facility). The accumulation fraction of 238Pu in individuals exposed to plutonium isotopes at the newer Spent Nuclear Fuel Reprocessing Plant ranged from 0.13% up to 27.5% based on the autopsy data. No statistically significant differences between 238Pu and 239Pu in distribution by the main organs of plutonium deposition were found in the Mayak workers. Based on the bioassay data,the fraction of 238Pu activity in urine is on average 38-69% of the total activity of 238Pu and 239Pu, which correlates with the isotopic composition in workplace air sampled at the Spent Nuclear Fuel Reprocessing Plant. In view of the higher specific activity of 238Pu, the contribution of 238Pu to the total internal dose, particularly in the skeleton and liver, might be expected to continue to increase, and continued surveillance is recommended.

  14. Electronic structure of {alpha}- and {delta}-Pu from photoelectron spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Arko, A. J. [Los Alamos National Laboratory, Los Alamos, New Mexico 87545 (United States); Joyce, J. J. [Los Alamos National Laboratory, Los Alamos, New Mexico 87545 (United States); Morales, L. [Los Alamos National Laboratory, Los Alamos, New Mexico 87545 (United States); Wills, J. [Los Alamos National Laboratory, Los Alamos, New Mexico 87545 (United States); Lashley, J. [Los Alamos National Laboratory, Los Alamos, New Mexico 87545 (United States); Wastin, F. [European Commission, Joint Research Centre, Institute for Transuranic Elements, P.O. Box 2340, D-76175 Karlsruhe, (Germany); Rebizant, J. [European Commission, Joint Research Centre, Institute for Transuranic Elements, P.O. Box 2340, D-76175 Karlsruhe, (Germany)

    2000-07-15

    We report photoemission results on {alpha}- and {delta}-Pu using a laser plasma light source (LPLS) as well as He light as the exciting radiation. The LPLS is a pseudocontinuum tunable light source with intensities rivaling some second-generation synchrotrons. Both phases of Pu display a narrow, temperature-independent, 5f-related feature at the Fermi energy, which is narrower in {delta}-Pu than in {alpha}-Pu, suggestive of possible heavy-fermion-like behavior. In both {alpha}-Pu and {delta}-Pu the photon-energy dependence of this feature suggests some 6d admixture, albeit somewhat smaller in {delta}-Pu. In this respect it differs qualitatively from Ce and U heavy fermions. (c) 2000 The American Physical Society.

  15. Plutonium stabilization and handling (PuSH)

    Energy Technology Data Exchange (ETDEWEB)

    Weiss, E.V.

    1997-01-23

    This Functional Design Criteria (FDC) addresses construction of a Stabilization and Packaging System (SPS) to oxidize and package for long term storage remaining plutonium-bearing special nuclear materials currently in inventory at the Plutonium Finishing Plant (PFP), and modification of vault equipment to allow storage of resulting packages of stabilized SNM for up to fifty years. The major sections of the project are: site preparation; SPS Procurement, Installation, and Testing; storage vault modification; and characterization equipment additions. The SPS will be procured as part of a Department of Energy nationwide common procurement. Specific design crit1460eria for the SPS have been extracted from that contract and are contained in an appendix to this document.

  16. Aggressive acute myeloid leukemia in PU.1/p53 double-mutant mice.

    Science.gov (United States)

    Basova, P; Pospisil, V; Savvulidi, F; Burda, P; Vargova, K; Stanek, L; Dluhosova, M; Kuzmova, E; Jonasova, A; Steidl, U; Laslo, P; Stopka, T

    2014-09-25

    PU.1 downregulation within hematopoietic stem and progenitor cells (HSPCs) is the primary mechanism for the development of acute myeloid leukemia (AML) in mice with homozygous deletion of the upstream regulatory element (URE) of PU.1 gene. p53 is a well-known tumor suppressor that is often mutated in human hematologic malignancies including AML and adds to their aggressiveness; however, its genetic deletion does not cause AML in mouse. Deletion of p53 in the PU.1(ure/ure) mice (PU.1(ure/ure)p53(-/-)) results in more aggressive AML with shortened overall survival. PU.1(ure/ure)p53(-/-) progenitors express significantly lower PU.1 levels. In addition to URE deletion we searched for other mechanisms that in the absence of p53 contribute to decreased PU.1 levels in PU.1(ure/ure)p53(-/-) mice. We found involvement of Myb and miR-155 in downregulation of PU.1 in aggressive murine AML. Upon inhibition of either Myb or miR-155 in vitro the AML progenitors restore PU.1 levels and lose leukemic cell growth similarly to PU.1 rescue. The MYB/miR-155/PU.1 axis is a target of p53 and is activated early after p53 loss as indicated by transient p53 knockdown. Furthermore, deregulation of both MYB and miR-155 coupled with PU.1 downregulation was observed in human AML, suggesting that MYB/miR-155/PU.1 mechanism may be involved in the pathogenesis of AML and its aggressiveness characterized by p53 mutation.

  17. Oxidative dissolution of unirradiated Mimas MOX fuel (U/Pu oxides) in carbonated water under oxic and anoxic conditions

    Science.gov (United States)

    Odorowski, Mélina; Jégou, Christophe; De Windt, Laurent; Broudic, Véronique; Peuget, Sylvain; Magnin, Magali; Tribet, Magaly; Martin, Christelle

    2016-01-01

    Few studies exist concerning the alteration of Mimas Mixed-OXide (MOX) fuel, a mixed plutonium and uranium oxide, and data is needed to better understand its behavior under leaching, especially for radioactive waste disposal. In this study, two leaching experiments were conducted on unirradiated MOX fuel with a strong alpha activity (1.3 × 109 Bq.gMOX-1 reproducing the alpha activity of spent MOX fuel with a burnup of 47 GWd·tHM-1 after 60 years of decay), one under air (oxic conditions) for 5 months and the other under argon (anoxic conditions with [O2] MOX pellets under both oxic and anoxic conditions were similar, demonstrating the predominant effect of alpha radiolysis on the oxidative dissolution of the pellets. The uranium released was found to be mostly in solution as carbonate species according to modeling, whereas the Am and Pu released were significantly sorbed or precipitated onto the TiO2 reactor. An intermediate fraction of Am (12%) was also present as colloids. SEM and EPMA results indicated a preferential dissolution of the UO2 matrix compared to the Pu-enriched agglomerates, and Raman spectroscopy showed the Pu-enriched agglomerates were slightly oxidized during leaching. Unlike Pu-enriched zones, the UO2 grains were much more sensitive to oxidative dissolution, but the presence of carbonates did not enable observation of an oxidized layer by Raman spectroscopy with the exception of a few areas revealing the presence of U4O9. This data shows the heterogeneous nature of the alteration and the need to combine information from different techniques to determine the origin of releases.

  18. Effects of aqueous extracts of raw pu-erh tea and ripened pu-erh tea on proliferation and differentiation of 3T3-L1 preadipocytes.

    Science.gov (United States)

    Cao, Zhen-Hui; Yang, Hui; He, Zhan-Long; Luo, Cheng; Xu, Zhi-Qiang; Gu, Da-Hai; Jia, Jun-Jing; Ge, Chang-Rong; Lin, Qiu-Ye

    2013-08-01

    Pu-erh tea has shown anti-obesity effects but little is known about its effect on proliferation and differentiation of preadipocytes. This study investigated the effects of the aqueous extracts of raw pu-erh tea and ripened pu-erh tea on proliferation and differentiation of murine 3T3-L1 preadiopocytes. We examined dose and time effects of both aqueous extracts on proliferation of 3T3-L1 preadipocytes. The contents of triglycerides in cytoplasm and the mRNA expression of critical transcriptional factors involved in differentiation were determined. Cytotoxicity and apoptosis rate of preadipocytes by pu-erh tea extracts treatment were test for toxic and pro-apoptotic effects. Both aqueous extracts of pu-erh tea inhibited the proliferation of 3T3-L1 preadipocytes at the selected time points. At lower concentration of raw pu-erh tea extracts (less than 300 µg/ml) and ripened pu-erh tea extracts (less than 350 µg/ml), no significant cytotoxic and pro-apoptotic were observed. Ripened pu-erh tea was more effective with lower IC50 than raw pu-erh tea. Both extracts suppressed the differentiation and down-regulated the gene expression of peroxisome proliferator-activated receptor-γ and CCAAT/enhancer binding proteins-α. Therefore, these results indicate that both aqueous extracts of pu-erh tea can inhibit proliferation and differentiation with ripened pu-erh tea more potent. Polyphenol rich in both extracts may play a role in the inhibition of proliferation and differentiation of 3T3-L1 preadipocytes.

  19. Plutonium concentration and (240)Pu/(239)Pu atom ratio in biota collected from Amchitka Island, Alaska: recent measurements using ICP-SFMS.

    Science.gov (United States)

    Bu, Kaixuan; Cizdziel, James V; Dasher, Douglas

    2013-10-01

    Three underground nuclear tests, including the Unites States' largest, were conducted on Amchitka Island, Alaska. Monitoring of the radiological environment around the island is challenging because of its remote location. In 2008, the Department of Energy (DOE) Office of Legacy Management (LM) became responsible for the long term maintenance and surveillance of the Amchitka site. The first DOE LM environmental survey occurred in 2011 and is part of a cycle of activities that will occur every 5 years. The University of Alaska Fairbanks, a participant in the 2011 study, provided the lichen (Cladonia spp.), freshwater moss (Fontinalis neomexicanus), kelp (Eualaria fistulosa) and horse mussel (Modiolus modiolus) samples from Amchitka Island and Adak Island (a control site). These samples were analyzed for (239)Pu and (240)Pu concentration and (240)Pu/(239)Pu atom ratio using inductively coupled plasma sector field mass spectrometry (ICP-SFMS). Plutonium concentrations and (240)Pu/(239)Pu atom ratios were generally consistent with previous terrestrial and marine studies in the region. The ((239)+)(240)Pu levels (mBq kg(-1), dry weight) ranged from 3.79 to 57.1 for lichen, 167-700 for kelp, 27.9-148 for horse mussel, and 560-573 for moss. Lichen from Adak Island had higher Pu concentrations than Amchitka Island, the difference was likely the result of the higher precipitation at Adak compared to Amchitka. The (240)Pu/(239)Pu atom ratios were significantly higher in marine samples compared to terrestrial and freshwater samples (t-test, p Pu occurred into the North Pacific Ocean, likely from the Marshall Island high yield nuclear tests, but other potential sources, such as the Kamchatka Peninsula Rybachiy Naval Base and Amchitka Island underground nuclear test site cannot be ruled out.

  20. Slow Neutron Velocity Spectrometer Transmission Studies Of Pu

    Science.gov (United States)

    Havens, W. W. Jr.; Melkonian, E.; Rainwater, L. J.; Levin, M.

    1951-05-28

    The slow neutron transmission of several samples of Pu has been investigated with the Columbia Neutron Velocity Spectrometer. Data are presented in two groups, those covering the energy region from 0 to 6 ev, and those covering the region above 6 ev. Below 6 ev the resolution was relatively good, and a detailed study of the cross section variation was made. Work above 6 ev consisted of merely locating levels and obtaining a rough idea of their strengths.

  1. Intrinsic Nanoscience of δ Pu-Ga Alloys: Local Structure and Speciation, Collective Behavior, Nanoscale Heterogeneity, and Aging Mechanisms

    Energy Technology Data Exchange (ETDEWEB)

    Conradson, Steven D.; Bock, Nicolas; Castro, Julio M.; Conradson, Dylan R.; Cox, Lawrence E.; Dmowski, Wojtek; Dooley, David E.; Egami, Takeshi; Espinosa-Faller, Francisco J.; Freibert, Franz J.; Garcia-Adeva, Angel J.; Hess, Nancy J.; Holmstrom, Erik; Howell, Rafael C.; Katz, Barbara A.; Lashley, Jason C.; Martinez, Raymond J.; Moore, David P.; Morales, Luis A.; Olivas, J David; Pereyra, Ramiro A.; Ramos, Michael; Terry, Jeff H.; Villella, Phillip M.

    2014-04-24

    Because diffraction measurements are sensitive only to the long range average arrangement of the atoms in the coherent portion of a crystal, complementary local structure measurements are required for a complete understanding of the structure of a complex material. This is particularly an issue in solid solutions where even random distributions of a solute will result in nanometer-scale fluctuations in the local composition. The structure will be further complicated if collective and cooperative phenomena organize the solute distribution via longer range interactions between non-bonded solute sites. If the solute affects the phase stability then the question is raised of whether the atoms in domains with local compositions outside the limits of the bulk phase will rearrange into the structure stable for that composition and temperature or if the resulting stress would prevent such a local phase transition. If the former, then phase separated, heterogeneous structures at or below the diffraction limit will form. This nanometerscale competition between the phase transition and the epitaxial mismatch – exacerbated by the added strain if the transition involves a volume change – raises the potential for the formation of novel structures that do not occur in bulk material, e.g., fcc Fe. This coupling over multiple scales between inhomogeneity ordering, elastic forces, phase competition, and texture in the form of coexisting structures is a hallmark of martensites, a class of complex materials that includes δ-stabilized PuGa and that often exhibit correlated atomic and electronic properties. The enigmatic and extreme nature of Pu is consistent with its exhibiting unusual structural behavior of this type, including nanoscale heterogeneity in δ-stabilized PuGa and its enhanced homogeneity on aging that has been suggested based on earlier X-ray Absorption Fine Structure (XAFS) spectroscopy and x-ray pair distribution function (pdf) measurements. Measurements on a

  2. Uso de contraceptivos por puérperas adolescentes

    Directory of Open Access Journals (Sweden)

    Fernanda Schulz da Rosa

    2014-07-01

    Full Text Available Objetivo: Indagar el uso de métodos contraceptivos por las puérperas adolescentes a fin de relacionar su (desuso con el embarazo en la adolescencia. Método: Estudio transversal, descriptivo, realizado por medio de un instrumento estructurado con 181 puérperas adolescentes que tuvieron sus partos en el hospital participante de la investigación. Los datos fueron recolectados en el período de diciembre de 2008 a diciembre de 2009. Resultados: El 64,1% de las puérperas usaba algún método contraceptivo antes del embarazo; los métodos más utilizados fueron el anticoncepcional oral (51% y el preservativo masculino (29%. Para el 75% de las adolescentes el embarazo fue planeado y justificado por el deseo y la voluntad propia de experimentar la maternidad. Conclusión: Considerando que casi la mitad de las adolescentes entrevistadas deseaba el embarazo, se deduce que investigar y discutir apenas el uso o no de los métodos contraceptivos no es adecuado. Es necesario profundizar las investigaciones acerca de los significados de ser madre en la adolescencia.

  3. Pu-238 assay performance with the Canberra IQ3 system

    Energy Technology Data Exchange (ETDEWEB)

    Booth, L.; Gillespie, B.; Seaman, G.

    1997-11-01

    Canberra Industries has recently completed a demonstration project at the Westinghouse Savannah River Site (WSRC) to characterize 55-gallon drums containing Pu-238 contaminated waste. The goal of this project was to detect and quantify Pu-238 contaminated waste. The goal of this project was to detect and quantify Pu-238 waste to detection limits of less than 50 nCi/g using gamma assay techniques. This would permit reclassification of these drums from transuranic (TRU) waste to low-level waste (LLW). The instrument used for this assay was a Canberra IQ3 high sensitivity gamma assay system, mounted in a trailer. The results of the measurements demonstrate achievement of detection levels as low as 1 nCi/g for low density waste drums, and good correlation with known concentrations in several test drums. In addition, the data demonstrates significant advantages for using large area low-energy germanium detectors for achieving the lowest possible MDAs for gamma rays in the 80-250 keV range. 1 fig., 2 tabs.

  4. Oxidation and reduction behaviors of a prototypic MgO-PuO2-x inert matrix fuel

    Science.gov (United States)

    Miwa, Shuhei; Osaka, Masahiko

    2017-04-01

    Oxidation and reduction behaviors of prototypic MgO-based inert matrix fuels (IMFs) containing PuO2-x were experimentally investigated by means of thermogravimetry. The oxidation and reduction kinetics of the MgO-PuO2-x specimen were determined. The oxidation and reduction rates of the MgO-PuO2-x were found to be low compared with those of PuO2-x. It is note that the changes in O/Pu ratios of MgO-PuO2-x from stoichiometry were smaller than those of PuO2-x at high oxygen partial pressure.

  5. 40 CFR 35.2025 - Allowance and advance of allowance.

    Science.gov (United States)

    2010-07-01

    ... facilities planning and design of the project and Step 7 agreements will include an allowance for facility planning in accordance with appendix B of this subpart. (b) Advance of allowance to potential grant... grant applicants for facilities planning and project design. (2) The State may request that the right to...

  6. Distribution characteristics of ¹³⁷Cs, Pu isotopes and ²⁴¹Am in soil in Korea.

    Science.gov (United States)

    Lee, S H; Oh, J S; Lee, J M; Lee, K B; Park, T S; Lujaniene, G; Valiulis, D; Sakalys, J

    2013-11-01

    Cesium-137, Plutonium isotopes and (241)Am were studied in soil samples collected from Korea between 2006 and 2008 to provide information on the distribution and origin of Pu isotopes and (241)Am. The vertical profiles of radionuclides showed higher activity concentrations at the surface layer and then gradually decreased with depth. A good correlation between (137)Cs and (239,240)Pu was observed, whereas a poor relationship between (137)Cs and (241)Am was found. The (238)Pu/(239,240)Pu, (241)Am/(239,240)Pu and (239,240)Pu/(137)Cs activity ratios were concordant to those of the global fallout ratios. Furthermore, the atomic ratios of (240)Pu/(239)Pu in the samples provided the information of Pu depositional history and the origin of Pu isotopes in Korea.

  7. An ab initio study of plutonium oxides surfaces; Etude ab initio des surfaces d'oxydes de Pu

    Energy Technology Data Exchange (ETDEWEB)

    Jomard, G.; Bottin, F.; Amadon, B

    2007-07-01

    By means of first-principles calculations, we have studied the atomic structure as well as the thermodynamic stability of various plutonium dioxide surfaces in function of their environment (in terms of oxygen partial pressure and temperature). All these simulations have been performed with the ABINIT code. It is well known that DFT fails to describe correctly plutonium-based materials since 5f electrons in such systems are strongly correlated. In order to go beyond DFT, we have treated PuO{sub 2} and {beta}-Pu{sub 2}O{sub 3} in a DFT+U framework. We show that the couple of parameters (U,J) that works well for pure Pu is also well designed for describing ground state (GS) properties of these two oxides. The major improvement with respect with DFT is that we are able to predict an insulating GS in agreement with experiments. The presence of a gap in the DOS (Density of States) of plutonium oxides should play a significant role in the predicted surface reactivity. However, performing DFT+U calculations on surfaces of plutonium oxide from scratch was too ambitious. That is why we decided, as a first step, to study the stability of the (100), (110) and (111) surfaces of PuO{sub 2} in a DFT-GGA framework. For each of these orientations, we considered various terminations. These ab initio results have been introduced in a thermodynamic model which allows us to predict the relative stability of the different terminations as a function of temperature and oxygen partial pressure (p{sub O{sub 2}}). We conclude that at room temperature and for p{sub O{sub 2}}{approx}10 atm., the polar O{sub 2}-(100) termination is favoured. The stabilization of such a polar stoichiometric surface is surprising and should be confirmed by DFT+U calculations before any final conclusion. (authors)

  8. Influence of the allotropic beta to alpha transformation and of oxygen on the distribution of plutonium in Zr-Pu and Ti-Pu dilute alloys

    CERN Document Server

    Languille, A; Remy, C

    1972-01-01

    Ti-Pu, Zr-Pu and Ti-U alloys, annealed above the transformation point, can show major segregation after cooling. The segregations increase with oxygen content. Annealing at high temperatures followed by severe quenching can cause them to disappear. (7 refs).

  9. Perturbation in the {sup 240}Pu/{sup 239}Pu global fallout ratio in local sediment following the nuclear accidents at Thule (Greenland) and Palomares (Spain)

    Energy Technology Data Exchange (ETDEWEB)

    Mitchell, P.I.; Vintro, L.L. [University Coll., Dublin (Ireland). Dept. of Physics; Dahlgaard, H. [Risoe National Lab., Roskilde (Denmark); Gasco, C.; Sanchez-Cabeza, J.A. [Barcelona Univ. (Spain). Dept. de Fisica Teorica

    1995-12-31

    It is well established that the main source of the plutonium found in marine sediments throughout the Northern Hemisphere is global stratospheric fallout, characterized by a typical {sup 240}Pu/{sup 239}Pu atom ratio of {approx}0.18. Measurements of perturbations in this ratio at various sites which had been subjected to close-in fallout, mainly from surface-based testing, has confirmed the feasibility of using this ratio to distinguish plutonium from different fallout sources. In the present study, the {sup 240}Pu/{sup 239}Pu ratio has been examined in samples of sediment collected at Thule (Greenland) and Palomares (Spain), where accidents involving the release and dispersion of plutonium from fractured nuclear weapons occurred in 1968 and 1966, respectively. The {sup 240}Pu/{sup 239}Pu ratio was measured by high-resolution alpha spectrometry and spectral deconvolution. The analytical results showed that at Thule the mean {sup 240}Pu/{sup 239}Pu atom ratio was 0.033{+-}0.004, while at Palomares the equivalent ratio appeared to be significantly higher at 0.056{+-}0.003. Both ratios are consistent with those reported for soils samples at the Nevada site and Nagasaki, and are clearly indicative of weapons-grade plutonium. 27 refs., 1 fig., 2 tabs.

  10. Carcinogenesis From Inhaled (PuO2)-Pu-239 in Beagles: Evidence for Radiation Homeostasis at Low Doses?

    Energy Technology Data Exchange (ETDEWEB)

    Fisher, Darrell R.; Weller, Richard E.

    2010-09-01

    From the early 1970s to the late 1980s, Pacific Northwest National Laboratory conducted life-span studies in beagle dogs on the biological effects of inhaled plutonium (239PuO2, 238PuO2, and 239Pu[NO3]4) to help predict risks associated with accidental intakes in workers. Years later, the purpose of the present follow-up study is to reassess the dose-response relationship for lung cancer induction in the 239PuO2 dogs compared to controls, with particular focus on the dose-response at low lung doses. A 239PuO2 aerosol (2.3 μm AMAD, 1.9 μm GSD) was administered to six groups of 20 young (18-month old) beagle dogs (10 males and 10 females) by inhalation at six different activity levels, as previously described in Laboratory reports. Control dogs were sham-exposed. In dose level 1, initial pulmonary lung depositions were 130 ± 48 Bq (3.5 ± 1.3 nCi), corresponding to 1 Bq g-1 lung tissue (0.029 ± 0.001 nCi g-1. Groups 2 through 6 received initial lung depositions (mean values) of 760, 2724, 10345, 37900, and 200000 Bq (22, 79, 300, 1100, and 5800 nCi) 239PuO2, respectively. For each dog, the absorbed dose to lungs was calculated from the initial lung burden and the final lung burden at time of death and lung mass, assuming a single, long-term retention function. Insoluble plutonium oxide exhibited long retention times in the lungs. Increased dose-dependent mortality due to lung cancer (bronchiolar-alveolar carcinoma, adenocarcinoma, epidermoid carcinoma) and radiation pneumonitis (highest exposures group) was observed in dogs exposed to 239PuO2. Calculated lung doses ranged from a few cGy in early-sacrificed dogs to 7764 cGy in dogs that experienced early deaths from radiation pneumonitis. Data were regrouped by lifetime lung dose and plotted as a function of lung tumor incidence. Lung tumor incidence in controls and zero-dose exposed dogs was 18% (5/28). However, no lung tumors were observed in 16 dogs with the lowest lung doses (8 to 22 cGy, mean 14.4 ± 7.6 c

  11. Polonium 210Po, uranium (234U, 238U and plutonium (238Pu, 239+240Pu bioaccumulation in marine birds

    Directory of Open Access Journals (Sweden)

    Strumińska-Parulska D. I.

    2013-04-01

    Full Text Available The aim of this work was the determination of 210Po, 234U, 238U, 238Pu and 239+240Pu concentration in marine birds which permanently or temporally live in the southern Baltic Sea coast. We chose 11 species of seabirds: three species permanently residing at southern Baltic Sea, four species of wintering birds and three species of migrating birds. The results show that analyzed radionuclides are non-uniformly distributed in the marine birds. The highest activities of 210Po were observed in feathers, muscles and liver. The highest uranium content was found in liver, rest of viscera and feathers, while plutonium in the digestion organs and feathers. Omnivore seabirds accumulated more polonium, plutonium than species that feed on fish, while herbivore seabirds accumulated more uranium than carnivore.

  12. Vertical distribution and migration of global fallout Pu in forest soils in southwestern China.

    Science.gov (United States)

    Bu, Wenting; Zheng, Jian; Guo, Qiuju; Uchida, Shigeo

    2014-10-01

    Soil samples collected in southwestern China were analyzed for Pu isotopes. The (240)Pu/(239)Pu atom ratios were around 0.18, which indicated the dominant source of global fallout. Consistent sub-surface maximums followed by exponential decline of (239+240)Pu activities in the soil cores were observed. Most of the Pu has still remained in the 0-10 cm layers since its deposition. Convection velocities and dispersion coefficients for Pu migration in the soils were estimated by the convection-dispersion equation (CDE) model. The effective convection velocities and effective dispersion coefficients ranged from 0.05 to 0.11 cm/y and from 0.06 to 0.29 cm(2)/y, respectively. Other factors that control the vertical migration of Pu in soil besides precipitation, soil particle size distribution and organic matter were suggested. Long-term migration behaviors of Pu in the soils were simulated. The results provide the Pu background baseline for further environmental monitoring and source identification of non-global fallout Pu inputs in the future.

  13. Mechanisms of in vivo binding site selection of the hematopoietic master transcription factor PU.1.

    Science.gov (United States)

    Pham, Thu-Hang; Minderjahn, Julia; Schmidl, Christian; Hoffmeister, Helen; Schmidhofer, Sandra; Chen, Wei; Längst, Gernot; Benner, Christopher; Rehli, Michael

    2013-07-01

    The transcription factor PU.1 is crucial for the development of many hematopoietic lineages and its binding patterns significantly change during differentiation processes. However, the 'rules' for binding or not-binding of potential binding sites are only partially understood. To unveil basic characteristics of PU.1 binding site selection in different cell types, we studied the binding properties of PU.1 during human macrophage differentiation. Using in vivo and in vitro binding assays, as well as computational prediction, we show that PU.1 selects its binding sites primarily based on sequence affinity, which results in the frequent autonomous binding of high affinity sites in DNase I inaccessible regions (25-45% of all occupied sites). Increasing PU.1 concentrations and the availability of cooperative transcription factor interactions during lineage differentiation both decrease affinity thresholds for in vivo binding and fine-tune cell type-specific PU.1 binding, which seems to be largely independent of DNA methylation. Occupied sites were predominantly detected in active chromatin domains, which are characterized by higher densities of PU.1 recognition sites and neighboring motifs for cooperative transcription factors. Our study supports a model of PU.1 binding control that involves motif-binding affinity, PU.1 concentration, cooperativeness with neighboring transcription factor sites and chromatin domain accessibility, which likely applies to all PU.1 expressing cells.

  14. PU/PVDF 防水透气共混膜的制备及性能研究%Preparation and characterization analysis of waterproof breathable PU/PVDF nanofibrous membranes

    Institute of Scientific and Technical Information of China (English)

    周颖; 姚理荣; 高强

    2014-01-01

    PU/PVDF nanofibrous membranes were successfully prepared by electrospinning .The effect of the concentration , the component solvent of DMF/acetone and mass ratio of solute on the morphology , the diameter of the spun fibers and the contact angle of fiber membrane were studied .The PU/PVDF membrane with optimum parameter was explored .The results show that the optimum process for electrospinning PU/PVDF membrane is concentration being 12%, volume ratio of component solvents of DMF/acetone being 4/6 , mass ratio of solute of PU/PVDF being 7/3 when voltage being 14 kV and traveling distance being 10 cm.Under these conditions , PU/PVDF blend membrane with good air permeability, excellent waterproofness and stretchability can be obtained .%采用静电纺丝法制备聚氨酯/聚偏氟乙烯( PU/PVDF )共混纳米纤维膜,研究PU、PVDF质量分数、溶剂体积配比、溶质质量比对纳米纤维形貌、直径及膜性能的影响,探索共混纤维膜较优制备工艺。结果表明:共混纳米纤维膜较优制备工艺为静电纺丝电压14 kV、接收距离10 cm、纺丝液质量分数12%、溶剂体积配比N,N-二甲基甲酰胺/丙酮为4/6、溶质质量比PU/PVDF为7/3,此条件下可获得具有较优防水透气性能和力学性能的共混膜。

  15. Characterization of ^{239,240}Pu Radionuclide Adsorption to Soil Particles and Mineral Dust Aerosols

    Science.gov (United States)

    Tatro, D. P.; Arimoto, R.; McMillan, N. J.; Barnes, M.

    2006-12-01

    The release of ^{239,240}Pu into the environment by nuclear weapons testing 50 years ago initiated the cyclic mobilization of Pu-contaminated soil particles via the resuspension of dust resulting in a widespread distribution of Pu and other radionuclides. It is unclear what enables the aeolian transport of Pu in the environment; plausible hypotheses of Pu binding to dust and soil particles include Pu adsorption to iron oxides/hydroxides, organic acids, or silicate minerals such as clays. To investigate the connections between surface soils, dust and radionuclides, samples of soil and/or dust were collected from the Project Gnome Site in Eddy County, NM, the Jemez Mountains near Los Alamos, NM, and two 50-year old attics and wind-blown dust in Big Spring, TX. This study tests the hypothesis that Pu is adsorbed onto Fe oxides and hydroxides that coat dust/soil particles. The samples are generally low in organic carbon (0.2 - 4.8%, except for the unburned Los Alamos sample at 9.4%), as measured by LOI (Loss On Ignition) at 360 °C. The citrate-bicarbonate-dithionite method (CDB) of Fe oxide removal, first proposed by Mehra and Jackson in 1960, was used to selectively extract Fe oxides from the samples while leaving silicate Fe intact. Chemical digestion of each sample creates two fractions, the extracted supernatant and a solid pellet residue. If the Pu were associated with Fe oxides, then Fe and Pu should both be selectively removed from the bulk sample during the CBD process, leaving the pellet depleted in Fe and Pu and the supernatant enriched. For Fe, this was confirmed by scanning electron microscope and petrographic analyses. Preliminary radiochemical analyses of Pu activity also verify this hypothesis. Pu activity is significantly lower in pellets than bulk samples (Pu activitypellet/Pu activitybulk average = 0.07, range 0.02-0.12); Pu activity in supernatants is significantly higher than in bulk samples (Pu activitysupernatant/Pu activitybulk average = 4

  16. Roles of PU.1 in monocyte- and mast cell-specific gene regulation: PU.1 transactivates CIITA pIV in cooperation with IFN-gamma.

    Science.gov (United States)

    Ito, Tomonobu; Nishiyama, Chiharu; Nakano, Nobuhiro; Nishiyama, Makoto; Usui, Yoshihiko; Takeda, Kazuyoshi; Kanada, Shunsuke; Fukuyama, Kanako; Akiba, Hisaya; Tokura, Tomoko; Hara, Mutsuko; Tsuboi, Ryoji; Ogawa, Hideoki; Okumura, Ko

    2009-07-01

    Over-expression of PU.1, a myeloid- and lymphoid-specific transcription factor belonging to the Ets family, induces monocyte-specific gene expression in mast cells. However, the effects of PU.1 on each target gene and the involvement of cytokine signaling in PU.1-mediated gene expression are largely unknown. In the present study, PU.1 was over-expressed in two different types of bone marrow-derived cultured mast cells (BMMCs): BMMCs cultured with IL-3 plus stem cell factor (SCF) and BMMCs cultured with pokeweed mitogen-stimulated spleen-conditioned medium (PWM-SCM). PU.1 over-expression induced expression of MHC class II, CD11b, CD11c and F4/80 on PWM-SCM-cultured BMMCs, whereas IL-3/SCF-cultured BMMCs expressed CD11b and F4/80, but not MHC class II or CD11c. When IFN-gamma was added to the IL-3/SCF-based medium, PU.1 transfectant acquired MHC class II expression, which was abolished by antibody neutralization or in Ifngr(-/-) BMMCs, through the induction of expression of the MHC class II transactivator, CIITA. Real-time PCR detected CIITA mRNA driven by the fourth promoter, pIV, and chromatin immunoprecipitation indicated direct binding of PU.1 to pIV in PU.1-over-expressing BMMCs. PU.1-over-expressing cells showed a marked increase in IL-6 production in response to LPS stimulation in both IL-3/SCF and PWM-SCM cultures. These results suggest that PU.1 overproduction alone is sufficient for both expression of CD11b and F4/80 and for amplification of LPS-induced IL-6 production. However, IFN-gamma stimulation is essential for PU.1-mediated transactivation of CIITA pIV. Reduced expression of mast cell-related molecules and transcription factors GATA-1/2 and up-regulation of C/EBPalpha in PU.1 transfectants indicate that enforced PU.1 suppresses mast cell-specific gene expression through these transcription factors.

  17. ARRAYS OF BOTTLES OF PLUTONIUM NITRATE SOLUTION

    Energy Technology Data Exchange (ETDEWEB)

    Margaret A. Marshall

    2012-09-01

    In October and November of 1981 thirteen approaches-to-critical were performed on a remote split table machine (RSTM) in the Critical Mass Laboratory of Pacific Northwest Laboratory (PNL) in Richland, Washington using planar arrays of polyethylene bottles filled with plutonium (Pu) nitrate solution. Arrays of up to sixteen bottles were used to measure the critical number of bottles and critical array spacing with a tight fitting Plexiglas® reflector on all sides of the arrays except the top. Some experiments used Plexiglas shells fitted around each bottles to determine the effect of moderation on criticality. Each bottle contained approximately 2.4 L of Pu(NO3)4 solution with a Pu content of 105 g Pu/L and a free acid molarity H+ of 5.1. The plutonium was of low 240Pu (2.9 wt.%) content. These experiments were sponsored by Rockwell Hanford Operations because of the lack of experimental data on the criticality of arrays of bottles of Pu solution such as might be found in storage and handling at the Purex Facility at Hanford. The results of these experiments were used “to provide benchmark data to validate calculational codes used in criticality safety assessments of [the] plant configurations” (Ref. 1). Data for this evaluation were collected from the published report (Ref. 1), the approach to critical logbook, the experimenter’s logbook, and communication with the primary experimenter, B. Michael Durst. Of the 13 experiments preformed 10 were evaluated. One of the experiments was not evaluated because it had been thrown out by the experimenter, one was not evaluated because it was a repeat of another experiment and the third was not evaluated because it reported the critical number of bottles as being greater than 25. Seven of the thirteen evaluated experiments were determined to be acceptable benchmark experiments. A similar experiment using uranyl nitrate was benchmarked as U233-SOL-THERM-014.

  18. Post-Irradiation Examination of 237Np Targets for 238Pu Production

    Energy Technology Data Exchange (ETDEWEB)

    Morris, Robert Noel [ORNL; Baldwin, Charles A [ORNL; Hobbs, Randy W [ORNL; Schmidlin, Joshua E [ORNL

    2015-01-01

    Oak Ridge National Laboratory is recovering the US 238Pu production capability and the first step in the process has been to evaluate the performance of a 237Np target cermet pellet encased in an aluminum clad. The process proceeded in 3 steps; the first step was to irradiate capsules of single pellets composed of NpO2 and aluminum power to examine their shrinkage and gas release. These pellets were formed by compressing sintered NpO2 and aluminum powder in a die at high pressure followed by sintering in a vacuum furnace. Three temperatures were chosen for sintering the solution precipitated NpO2 power used for pellet fabrication. The second step was to irradiate partial targets composed of 8 pellets in a semi-prototypical arrangement at the two best performing sintering temperatures to determine which temperature gave a pellet that performed the best under the actual planned irradiation conditions. The third step was to irradiate ~50 pellets in an actual target configuration at design irradiation conditions to assess pellet shrinkage and gas release, target heat transfer, and dimensional stability. The higher sintering temperature appeared to offer the best performance after one cycle of irradiation by having the least shrinkage, thus keeping the heat transfer gap between the pellets and clad small minimizing the pellet operating temperature. The final result of the testing was a target that can meet the initial production goals, satisfy the reactor safety requirements, and can be fabricated in production quantities. The current focus of the program is to verify that the target can be remotely dissembled, the pellets dissolved, and the 238Pu recovered. Tests are being conducted to examine these concerns and to compare results to code predictions. Once the performance of the full length targets has been quantified, the pellet 237Np loading will be revisited to determine if it can be

  19. The transcription factor PU.1 promotes alternative macrophage polarization and asthmatic airway inflammation.

    Science.gov (United States)

    Qian, Feng; Deng, Jing; Lee, Yong Gyu; Zhu, Jimmy; Karpurapu, Manjula; Chung, Sangwoon; Zheng, Jun-Nian; Xiao, Lei; Park, Gye Young; Christman, John W

    2015-12-01

    The transcription factor PU.1 is involved in regulation of macrophage differentiation and maturation. However, the role of PU.1 in alternatively activated macrophage (AAM) and asthmatic inflammation has yet been investigated. Here we report that PU.1 serves as a critical regulator of AAM polarization and promotes the pathological progress of asthmatic airway inflammation. In response to the challenge of DRA (dust mite, ragweed, and Aspergillus) allergens, conditional PU.1-deficient (PU/ER(T)(+/-)) mice displayed attenuated allergic airway inflammation, including decreased alveolar eosinophil infiltration and reduced production of IgE, which were associated with decreased mucous glands and goblet cell hyperplasia. The reduced asthmatic inflammation in PU/ER(T)(+/-) mice was restored by adoptive transfer of IL-4-induced wild-type (WT) macrophages. Moreover, after treating PU/ER(T)(+/-) mice with tamoxifen to rescue PU.1 function, the allergic asthmatic inflammation was significantly restored. In vitro studies demonstrate that treatment of PU.1-deficient macrophages with IL-4 attenuated the expression of chitinase 3-like 3 (Ym-1) and resistin-like molecule alpha 1 (Fizz-1), two specific markers of AAM polarization. In addition, PU.1 expression in macrophages was inducible in response to IL-4 challenge, which was associated with phosphorylation of signal transducer and activator of transcription 6 (STAT6). Furthermore, DRA challenge in sensitized mice almost abrogated gene expression of Ym-1 and Fizz-1 in lung tissues of PU/ER(T)(+/-) mice compared with WT mice. These data, all together, indicate that PU.1 plays a critical role in AAM polarization and asthmatic inflammation.

  20. Formulation of the Linear Response Theory in Relativistic LAPW Method. Calculation of Forces in Alpha-Pu

    Energy Technology Data Exchange (ETDEWEB)

    Kutepov, A L

    2004-01-08

    Linear-response (LR) theory in combination with the first-principles band structure codes allows to calculate phonons in an efficient way. In this report a formalism which enables us to apply LR theory within an all-electron framework utilizing the relativistic full-potential linearized augmented plane-wave (RFLAPW) method is presented. As first part, the equations for the calculations of the atomic forces are given and they are used for the calculation of forces in {alpha}-Pu. As a second step, a complete set of formulaes for the dynamic matrices calculation is presented.

  1. α-accompanied cold ternary fission of Pu-244238 isotopes in equatorial and collinear configuration

    Science.gov (United States)

    Santhosh, K. P.; Krishnan, Sreejith; Priyanka, B.

    2015-04-01

    The cold ternary fission of 238Pu, 240Pu, 242Pu, and 244Pu isotopes, with 4He as light charged particle, in equatorial and collinear configuration has been studied within the unified ternary fission model. The fragment combination 100Zr+4He+134Te possessing the near doubly magic nuclei 134Te(N =82 ,Z =52 ) gives the highest yield in the α-accompanied ternary fission of 238Pu. For the α-accompanied ternary fission of 240Pu, 242Pu, and 244Pu isotopes, the highest yield was found for the fragment combination with doubly magic nuclei 132Sn(N =82 ,Z =50 ) as the heavier fragment. The deformation and orientation of fragments have also been taken into account for the α-accompanied ternary fission of Pu-244238 isotopes, and it has been found that, in addition to the closed-shell effect, ground-state deformation also plays an important role in determining the isotopic yield in the ternary fission process. The emission probability and kinetic energy of long-range α particles have been calculated and are found to be in good agreement with the experimental data.

  2. A Method for Continuous (239)Pu Determinations in Arctic and Antarctic Ice Cores.

    Science.gov (United States)

    Arienzo, M M; McConnell, J R; Chellman, N; Criscitiello, A S; Curran, M; Fritzsche, D; Kipfstuhl, S; Mulvaney, R; Nolan, M; Opel, T; Sigl, M; Steffensen, J P

    2016-07-05

    Atmospheric nuclear weapons testing (NWT) resulted in the injection of plutonium (Pu) into the atmosphere and subsequent global deposition. We present a new method for continuous semiquantitative measurement of (239)Pu in ice cores, which was used to develop annual records of fallout from NWT in ten ice cores from Greenland and Antarctica. The (239)Pu was measured directly using an inductively coupled plasma-sector field mass spectrometer, thereby reducing analysis time and increasing depth-resolution with respect to previous methods. To validate this method, we compared our one year averaged results to published (239)Pu records and other records of NWT. The (239)Pu profiles from the Arctic ice cores reflected global trends in NWT and were in agreement with discrete Pu profiles from lower latitude ice cores. The (239)Pu measurements in the Antarctic ice cores tracked low latitude NWT, consistent with previously published discrete records from Antarctica. Advantages of the continuous (239)Pu measurement method are (1) reduced sample preparation and analysis time; (2) no requirement for additional ice samples for NWT fallout determinations; (3) measurements are exactly coregistered with all other chemical, elemental, isotopic, and gas measurements from the continuous analytical system; and (4) the long half-life means the (239)Pu record is stable through time.

  3. Pharmacologic efficacy of PU.1 inhibition by heterocyclic dications: a mechanistic analysis.

    Science.gov (United States)

    Stephens, Dominique C; Kim, Hye Mi; Kumar, Arvind; Farahat, Abdelbasset A; Boykin, David W; K Poon, Gregory M

    2016-05-19

    Heterocyclic dications are receiving increasing attention as targeted inhibitors of transcription factors. While many dications act as purely competitive inhibitors, some fail to displace protein efficiently at drug concentrations expected to saturate their DNA target. To achieve a mechanistic understanding of these non-competitive effects, we used a combination of dications, which are intrinsically fluorescent and spectrally-separated fluorescently labeled DNA to dissect complex interactions in multi-component drug/DNA/protein systems. Specifically, we interrogated site-specific binding by the transcription factor PU.1 and its perturbation by DB270, a furan-bisbenzimidazole-diamidine that strongly targets PU.1 binding sites yet poorly inhibits PU.1/DNA complexes. By titrating DB270 and/or cyanine-labeled DNA with protein or unlabeled DNA, and following the changes in their fluorescence polarization, we found direct evidence that DB270 bound protein independently of their mutual affinities for sequence-specific DNA. Each of the three species competed for the other two, and this interplay of mutually dependent equilibria abrogated DB270's inhibitory activity, which was substantively restored under conditions that attenuated DB270/PU.1 binding. PU.1 binding was consistent with DB270's poor inhibitory efficacy of PU.1 in vivo, while its isosteric selenophene analog (DB1976), which did not bind PU.1 and strongly inhibited the PU.1/DNA complex in vitro, fully antagonized PU.1-dependent transactivation in vivo.

  4. E2A Antagonizes PU.1 Activity through Inhibition of DNA Binding.

    Science.gov (United States)

    Rogers, Jason H; Owens, Kristin S; Kurkewich, Jeffrey; Klopfenstein, Nathan; Iyer, Sangeeta R; Simon, M Celeste; Dahl, Richard

    2016-01-01

    Antagonistic interactions between transcription factors contribute to cell fate decisions made by multipotent hematopoietic progenitor cells. Concentration of the transcription factor PU.1 affects myeloid/lymphoid development with high levels of PU.1 directing myeloid cell fate acquisition at the expense of B cell differentiation. High levels of PU.1 may be required for myelopoiesis in order to overcome inhibition of its activity by transcription factors that promote B cell development. The B cell transcription factors, E2A and EBF, are necessary for commitment of multipotential progenitors and lymphoid primed multipotential progenitors to lymphocytes. In this report we hypothesized that factors required for early B cell commitment would bind to PU.1 and antagonize its ability to induce myeloid differentiation. We investigated whether E2A and/or EBF associate with PU.1. We observed that the E2A component, E47, but not EBF, directly binds to PU.1. Additionally E47 represses PU.1-dependent transactivation of the MCSFR promoter through antagonizing PU.1's ability to bind to DNA. Exogenous E47 expression in hematopoietic cells inhibits myeloid differentiation. Our data suggest that E2A antagonism of PU.1 activity contributes to its ability to commit multipotential hematopoietic progenitors to the lymphoid lineages.

  5. E2A Antagonizes PU.1 Activity through Inhibition of DNA Binding

    Directory of Open Access Journals (Sweden)

    Jason H. Rogers

    2016-01-01

    Full Text Available Antagonistic interactions between transcription factors contribute to cell fate decisions made by multipotent hematopoietic progenitor cells. Concentration of the transcription factor PU.1 affects myeloid/lymphoid development with high levels of PU.1 directing myeloid cell fate acquisition at the expense of B cell differentiation. High levels of PU.1 may be required for myelopoiesis in order to overcome inhibition of its activity by transcription factors that promote B cell development. The B cell transcription factors, E2A and EBF, are necessary for commitment of multipotential progenitors and lymphoid primed multipotential progenitors to lymphocytes. In this report we hypothesized that factors required for early B cell commitment would bind to PU.1 and antagonize its ability to induce myeloid differentiation. We investigated whether E2A and/or EBF associate with PU.1. We observed that the E2A component, E47, but not EBF, directly binds to PU.1. Additionally E47 represses PU.1-dependent transactivation of the MCSFR promoter through antagonizing PU.1’s ability to bind to DNA. Exogenous E47 expression in hematopoietic cells inhibits myeloid differentiation. Our data suggest that E2A antagonism of PU.1 activity contributes to its ability to commit multipotential hematopoietic progenitors to the lymphoid lineages.

  6. Transport of (137)Cs, (241)Am and Pu isotopes in the Curonian Lagoon and the Baltic Sea.

    Science.gov (United States)

    Lujanienė, G; Remeikaitė-Nikienė, N; Garnaga, G; Jokšas, K; Šilobritienė, B; Stankevičius, A; Šemčuk, S; Kulakauskaitė, I

    2014-01-01

    Activities of (137)Cs, (241)Am and (239,240)Pu were analyzed with special emphasis on better understanding of radionuclide transport from land via the Neman River estuaries to the Baltic Sea and behavior in the marine environment. Although activity concentrations of (137)Cs in water samples collected the Baltic Sea were almost 100 times higher as compared to the Curonian Lagoon, its activities in the bottom sediments were found to be comparable. Activity (238)Pu/(239,240)Pu and atom (240)Pu/(239)Pu ratios indicated a different contribution of the Chernobyl-originated Pu to the suspended particulate matter (SPM) and bottom sediments. The largest amount of the Chernobyl-derived Pu was found in the smallest suspended matter particles of 0.2-1 μm in size collected in the Klaipeda Strait in 2011-2012. The decrease of characteristic activity (238)Pu/(239,240)Pu and atom (240)Pu/(239)Pu ratios towards the global fallout ones in surface soil and the corresponding increase of plutonium (Pu) ratios in the suspended particulate matter and bottom sediments have indicated that the Chernobyl-derived Pu, primarily deposited on the soil surface, was washed out and transported to the Baltic Sea. Behavior of (241)Am was found to be similar to that of Pu isotopes.

  7. Ternary fission yields of 241Pu(nth,f)

    Science.gov (United States)

    Köster, Ulli; Faust, Herbert; Fioni, Gabriele; Friedrichs, Thomas; Groß, Martin; Oberstedt, Stephan

    1998-10-01

    Ternary events in the thermal neutron induced fission of 241Pu were studied with the recoil separator LOHENGRIN at the Institut Laue Langevin in Grenoble. Yields and energy distributions could be determined for most isotopes of the elements hydrogen to oxygen. Also several heavier nuclei up to 30Mg could be observed. Yields were measured for 42 isotopes, for further 17 isotopes upper limits could be deduced. For the first time the halo nuclei 11Li and 14Be were found in neutron induced fission with yields of some 10-10 per fission. This is orders of magnitude lower than predicted by most of the ternary fission models.

  8. Modeling of constituent redistribution in U Pu Zr metallic fuel

    Science.gov (United States)

    Kim, Yeon Soo; Hayes, S. L.; Hofman, G. L.; Yacout, A. M.

    2006-12-01

    A computer model was developed to analyze constituent redistribution in U-Pu-Zr metallic nuclear fuels. Diffusion and thermochemical properties were parametrically determined to fit the postirradiation data from a fuel test performed in the Experimental Breeder Reactor II (EBR-II). The computer model was used to estimate redistribution profiles of fuels proposed for the conceptual designs of small modular fast reactors. The model results showed that the level of redistribution of the fuel constituents of the designs was similar to the measured data from EBR-II.

  9. Bulk media assay using backscattered Pu-Be neutrons

    CERN Document Server

    Csikai, J

    1999-01-01

    Spectral yields of elastically backscattered Pu-Be neutrons measured for graphite, water, polyethylene, liquid nitrogen, paraffin oil, SiO sub 2 , Al, Fe, and Pb slabs show a definite correlation with the energy dependence of the elastic scattering cross sections, sigma sub E sub L (E sub n). The C, N and O can be identified by the different structures in their sigma sub E sub L (E sub n) functions. The integrated spectral yields versus thickness exhibit saturation for each sample. The interrogated volume is limited by the presence of hydrogen in the sample. (author)

  10. The alpha-decay of Pu-236 to U-232

    Science.gov (United States)

    Ardisson, G.; Bosschot, J. M.; Hussonnois, M.; Le Du, J. F.; Trubert, D.; Lederer, C. M.

    1994-10-01

    The gamma-spectrum following the alpha-decay of Pu-236 was reinvestigated using a high resolution HPGe detector. The energy and intensity of 26 gamma-transitions were measured accurately; 21 of these were observed for the first time. All gamma-rays were placed in a U-232 level scheme accounting for 13 levels of which 8 are reported for the first time. The ground state rotational band was found to be fed up to spin I (sup pi) = 8(sup +) and the K(sup pi) = 0(sup-) octupole band to be fed up to I = 5.

  11. Refined data on the PuO{sub 4} volatility

    Energy Technology Data Exchange (ETDEWEB)

    Domanov, V.P.; Lobanov, Yu.V. [Joint Institute for Nuclear Research, Dubna (Russian Federation)

    2004-07-01

    In thermochromatographic (TC) studies on the thermal oxidation of trace quantities of plutonium in a stream of a He+O{sub 2} mixture, the formation of some volatile forms was observed. The most volatile compound was adsorbed on a quartz surface at a negative temperature of about -100 C. In the ref., we assumed that this adsorption zone could be related to the deposition of octovalent plutonium in the form of PuO{sub 4}. Later the correctness of this assumption was shown. (orig.)

  12. In vivo determination of nitrogen using Pu-Be sources.

    Science.gov (United States)

    Mernagh, J R; Harrison, J E; McNeill, K G

    1977-09-01

    A mehtod of measuring body nitrogen by neutron capture gamma analysis is described. The neutron flux is provided by four collimated 5 Ci Pu-Be sources, placed to give a bilateral irradiation of the subject. The 10-83 MeV thermal neutron capture gamma rays from 14N are detected by two heavily shielded 5 in X 4 in NaI(Tl) detectors. Results indicate a reproducibility +/-3% (1 SD) for a 10 min irradiation of the chest area, while giving a radiation dose equivalent of 50 mREM.

  13. First-principles elastic properties of (alpha)-Pu

    Energy Technology Data Exchange (ETDEWEB)

    Soderlind, P; Klepeis, J E

    2008-11-04

    Density-functional electronic structure calculations have been used to investigate the ambient pressure and low temperature elastic properties of the ground-state {alpha} phase of plutonium metal. The electronic structure and correlation effects are modeled within a fully relativistic anti-ferromagnetic treatment with a generalized gradient approximation for the electron exchange and correlation functionals. The 13 independent elastic constants, for the monoclinic {alpha}-Pu system, are calculated for the observed geometry. A comparison of the results with measured data from resonant ultrasound spectroscopy for a cast sample is made.

  14. Complicaciones en las puérperas laparotomizadas de urgencia

    OpenAIRE

    Victor Manuel Sierra Alfonso

    2014-01-01

    La presencia de una complicación intrabdominal postoperatoria después de una laparotomía agrava el estado de salud del paciente y ensombrece el pronóstico, a pesar del uso adecuado de antimicrobianos, de la correcta nutrición y de las ventajas de los cuidados intensivos. Se realizó un estudio retrospectivo descriptivo, con el objetivo de caracterizar las complicaciones en las puérperas, a las que se les practicaron laparotomías de urgencia. Se analizaron las referidas pacientes atendidas en e...

  15. First-principles elastic properties of (alpha)-Pu

    Energy Technology Data Exchange (ETDEWEB)

    Soderlind, P; Klepeis, J

    2009-02-18

    Density-functional electronic-structure calculations have been used to investigate the ambient pressure and low temperature elastic properties of the ground-state {alpha} phase of plutonium metal. The electronic structure and correlation effects are modeled within a fully relativistic antiferromagnetic treatment with a generalized gradient approximation for the electron exchange and correlation functional. The 13 independent elastic constants, for the monoclinic {alpha}-Pu system, are calculated for the observed geometry. A comparison of the results with measured data from recent resonant ultrasound spectroscopy for a cast sample is made.

  16. Neutron Resonance Parameters and Covariance Matrix of 239Pu

    Energy Technology Data Exchange (ETDEWEB)

    Derrien, Herve [ORNL; Leal, Luiz C [ORNL; Larson, Nancy M [ORNL

    2008-08-01

    In order to obtain the resonance parameters in a single energy range and the corresponding covariance matrix, a reevaluation of 239Pu was performed with the code SAMMY. The most recent experimental data were analyzed or reanalyzed in the energy range thermal to 2.5 keV. The normalization of the fission cross section data was reconsidered by taking into account the most recent measurements of Weston et al. and Wagemans et al. A full resonance parameter covariance matrix was generated. The method used to obtain realistic uncertainties on the average cross section calculated by SAMMY or other processing codes was examined.

  17. PU.1 antisense lncRNA against its mRNA translation promotes adipogenesis in porcine preadipocytes.

    Science.gov (United States)

    Wei, N; Wang, Y; Xu, R-X; Wang, G-Q; Xiong, Y; Yu, T-Y; Yang, G-S; Pang, W-J

    2015-04-01

    Antisense long non-coding RNAs (AS lncRNAs) play important roles in refined regulation of animal gene expression. However, their functions and molecular mechanisms for domestic animal adipogenesis are largely unknown. Here, we found a novel AS lncRNA transcribed from the porcine PU.1 gene (also known as SPI1) by strand-specific RT-PCR. Results showed that PU.1 AS lncRNA was expressed and generally lower than the level of PU.1 mRNA in porcine subcutaneous adipose, heart, liver, spleen, lympha, skeletal muscle and kidney tissues. We further found that the levels of PU.1 mRNA and PU.1 protein were significantly lower in subcutaneous and intermuscular adipose than in mesenteric and greater omentum adipose, whereas the levels of PU.1 AS lncRNA showed no difference in porcine adipose tissues from four different parts of the body. During porcine adipogenesis, levels of PU.1 mRNA increased at day 2 and then gradually decreased. Meanwhile, PU.1 AS lncRNA exhibited an expression trend similar to PU.1 mRNA but sharply decreased after day 2. Interestingly, PU.1 protein level rose during differentiation. In addition, at day 6 after differentiation, knockdown of endogenous PU.1 promoted adipogenesis, whereas knockdown of endogenous PU.1 AS lncRNA had the opposite effect. Moreover, peroxisome proliferator-activated receptor gamma (PPARG) and fatty acid synthase (FASN) were significantly upregulated in the PU.1 shRNA treatment group (P PU.1 AS shRNA treatment group (P PU.1 mRNA/PU.1 AS lncRNA duplex was detected by an endogenous ribonuclease protection assay combined with RT-PCR. Based on the above results, we suggest that PU.1 AS lncRNA (vs. its mRNA translation) promotes adipogenesis through the formation of a sense-antisense RNA duplex with PU.1 mRNA.

  18. On the Multi-Reference Nature of Plutonium Oxides: PuO$_2^{2+}$, PuO$_2$, PuO$_3$ and PuO$_2$(OH)$_2$

    CERN Document Server

    Boguslawski, Katharina; Tecmer, Paweł; Duperrouzel, Corinne; Gomes, André Severo Pereira; Legeza, Örs; Ayers, Paul W; Vallet, Valérie

    2016-01-01

    Actinide-containing complexes present formidable challenges for electronic structure methods due to the large number of degenerate or quasi-degenerate electronic states arising from partially occupied 5f and 6d shells. Conventional multi-reference methods can treat active spaces that are often at the upper limit of what is required for a proper treatment of species with complex electronic structures, leaving no room for verifying their suitability. In this work we address the issue of properly defining the active spaces in such calculations, and introduce a protocol to determine optimal active spaces based on the use of the Density Matrix Renormalization Group algorithm and concepts of quantum information theory. We apply the protocol to elucidate the electronic structure and bonding mechanism of volatile plutonium oxides (PuO$_3$ and PuO$_2$(OH)$_2$), species associated with nuclear safety issues for which little is known about the electronic structure and energetics. We show how, within a scalar relativisti...

  19. Complicaciones en las puérperas laparotomizadas de urgencia

    Directory of Open Access Journals (Sweden)

    Victor Manuel Sierra Alfonso

    2014-11-01

    Full Text Available La presencia de una complicación intrabdominal postoperatoria después de una laparotomía agrava el estado de salud del paciente y ensombrece el pronóstico, a pesar del uso adecuado de antimicrobianos, de la correcta nutrición y de las ventajas de los cuidados intensivos. Se realizó un estudio retrospectivo descriptivo, con el objetivo de caracterizar las complicaciones en las puérperas, a las que se les practicaron laparotomías de urgencia. Se analizaron las referidas pacientes atendidas en el Hospital Ginecoobstétrico “Piti Fajardo” y en el Hospital General Docente “Aleida Fernández Chardiet”, en el periodo comprendido entre enero del 2010 y diciembre del 2012. La muestra quedó conformada por nueve pacientes. Las complicaciones más presentadas fueron los trastornos hidroelectrolíticos y los trastornos del equilibrio ácido básico. No hubo muerte materna ni fetal. Las puérperas que más complicaciones presentaron fueron las de 35 años y más, con diagnóstico de placenta acreta, hematoma de la cúpula vaginal y atonía uterina. El tiempo de evolución hasta el tratamiento definitivo fue menor de 12 horas

  20. Thermal Analysis of ZPPR High Pu Content Stored Fuel

    Directory of Open Access Journals (Sweden)

    Charles W. Solbrig

    2014-01-01

    Full Text Available The Zero Power Physics Reactor (ZPPR operated from April 18, 1969, until 1990. ZPPR operated at low power for testing nuclear reactor designs. This paper examines the temperature of Pu content ZPPR fuel while it is in storage. Heat is generated in the fuel due to Pu and Am decay and is a concern for possible cladding damage. Damage to the cladding could lead to fuel hydriding and oxidizing. A series of computer simulations were made to determine the range of temperatures potentially occuring in the ZPPR fuel. The maximum calculated fuel temperature is 292°C (558°F. Conservative assumptions in the model intentionally overestimate temperatures. The stored fuel temperatures are dependent on the distribution of fuel in the surrounding storage compartments, the heat generation rate of the fuel, and the orientation of fuel. Direct fuel temperatures could not be measured but storage bin doors, storage sleeve doors, and storage canister temperatures were measured. Comparison of these three temperatures to the calculations indicates that the temperatures calculated with conservative assumptions are, as expected, higher than the actual temperatures. The maximum calculated fuel temperature with the most conservative assumptions is significantly below the fuel failure criterion of 600°C (1,112°F.

  1. NQR Study of the Heavy-Fermion Pu-115 Superconductors

    Science.gov (United States)

    Koutroulakis, G.; Yasuoka, H.; Tobash, P. H.; Mitchell, J. N.; Bauer, E. D.; Thompson, J. D.

    2014-03-01

    We present 115In nuclear quadrupolar resonance (NQR) measurements on the heavy-fermion superconductors Pu MIn5 (M=Co, Rh; Tc=2.5K, 1.6K, respectively), in the temperature range 0 . 29 K <= T <= 100 K . From the identified spectral lines, we deduce the quadrupolar parameters for the two inequivalent In sites, which are found to be qualitatively similar to those for other Ce- and Pu-115s. The quadrupolar frequency νQ varies with temperature in the normal state as per the empirical formula for conventional metals. As superconductivity develops, however, νQ exhibits a sharp, albeit small shift, which is a key prediction of the theory of composite superconducting (SC) pairing. The temperature variation of the nuclear spin-lattice relaxation rate T1- 1 delineates distinctive regimes of dynamic behavior. An excess of strong in-plane antiferromagnetic spin fluctuations is observed in the vicinity of Tc, which are believed to be playing a central role in the formation of the SC condensate. Analysis of the T1- 1 data in the SC state suggests that these compounds are strong-coupling d-wave superconductors.

  2. On the multi-reference nature of plutonium oxides: PuO2(2+), PuO2, PuO3 and PuO2(OH)2.

    Science.gov (United States)

    Boguslawski, Katharina; Réal, Florent; Tecmer, Paweł; Duperrouzel, Corinne; Gomes, André Severo Pereira; Legeza, Örs; Ayers, Paul W; Vallet, Valérie

    2017-02-08

    Actinide-containing complexes present formidable challenges for electronic structure methods due to the large number of degenerate or quasi-degenerate electronic states arising from partially occupied 5f and 6d shells. Conventional multi-reference methods can treat active spaces that are often at the upper limit of what is required for a proper treatment of species with complex electronic structures, leaving no room for verifying their suitability. In this work we address the issue of properly defining the active spaces in such calculations, and introduce a protocol to determine optimal active spaces based on the use of the Density Matrix Renormalization Group algorithm and concepts of quantum information theory. We apply the protocol to elucidate the electronic structure and bonding mechanism of volatile plutonium oxides (PuO3 and PuO2(OH)2), species associated with nuclear safety issues for which little is known about the electronic structure and energetics. We show how, within a scalar relativistic framework, orbital-pair correlations can be used to guide the definition of optimal active spaces which provide an accurate description of static/non-dynamic electron correlation, as well as to analyse the chemical bonding beyond a simple orbital model. From this bonding analysis we are able to show that the addition of oxo- or hydroxo-groups to the plutonium dioxide species considerably changes the π-bonding mechanism with respect to the bare triatomics, resulting in bent structures with a considerable multi-reference character.

  3. Electronic structure and chemical bond nature in Cs2PuO2Cl4

    Directory of Open Access Journals (Sweden)

    Teterin Yury A.

    2015-01-01

    Full Text Available X-ray photoelectron spectral analysis of dicaesiumtetrachlorodioxoplutonate (Cs2PuO2Cl4 single crystal was done in the binding energy range 0-~35 eV on the basis of binding energies and structure of the core electronic shells (~35 eV-1250 eV, as well as the relativistic discrete variation calculation results for the PuO2Cl4 (D4h. This cluster reflects Pu close environment in Cs2PuO2Cl4 containing the plutonyl group PuO2. The many-body effects due to the presence of cesium and chlorine were shown to contribute to the outer valence (0-~15 eV binding energy spectral structure much less than to the inner valence (~15 eV- ~35 eV binding energy one. The filled Pu 5f electronic states were theoretically calculated and experimentally con- firmed to present in the valence band of Cs2PuO2Cl4. It corroborates the suggestion on the direct participation of the Pu 5f electrons in the chemical bond. The Pu 6p atomic orbitals were shown to participate in formation of both the inner and the outer valence molecular orbitals (bands, while the filled Pu 6p and O 2s, Cl 3s electronic shells were found to take the largest part in formation of the inner valence molecular orbitals. The composition of molecular orbitals and the sequence order in the binding energy range 0-~35 eV in Cs2PuO2Cl4 were established. The quantitative scheme of molecular orbitals for Cs2PuO2Cl4 in the binding energy range 0-~15 eV was built on the basis of the experimental and theoretical data. It is fundamental for both understanding the chemical bond nature in Cs2PuO2Cl4 and the interpretation of other X-ray spectra of Cs2PuO2Cl4. The contributions to the chemical binding for the PuO2Cl4 cluster were evaluated to be: the contribution of the outer valence molecular orbitals -66 %, the contribution of the inner valence molecular orbitals -34 %.

  4. Chronology of Pu isotopes and 236U in an Arctic ice core.

    Science.gov (United States)

    Wendel, C C; Oughton, D H; Lind, O C; Skipperud, L; Fifield, L K; Isaksson, E; Tims, S G; Salbu, B

    2013-09-01

    In the present work, state of the art isotopic fingerprinting techniques are applied to an Arctic ice core in order to quantify deposition of U and Pu, and to identify possible tropospheric transport of debris from former Soviet Union test sites Semipalatinsk (Central Asia) and Novaya Zemlya (Arctic Ocean). An ice core chronology of (236)U, (239)Pu, and (240)Pu concentrations, and atom ratios, measured by accelerator mass spectrometry in a 28.6m deep ice core from the Austfonna glacier at Nordaustlandet, Svalbard is presented. The ice core chronology corresponds to the period 1949 to 1999. The main sources of Pu and (236)U contamination in the Arctic were the atmospheric nuclear detonations in the period 1945 to 1980, as global fallout, and tropospheric fallout from the former Soviet Union test sites Novaya Zemlya and Semipalatinsk. Activity concentrations of (239+240)Pu ranged from 0.008 to 0.254 mBq cm(-2) and (236)U from 0.0039 to 0.053 μBq cm(-2). Concentrations varied in concordance with (137)Cs concentrations in the same ice core. In contrast to previous published results, the concentrations of Pu and (236)U were found to be higher at depths corresponding to the pre-moratorium period (1949 to 1959) than to the post-moratorium period (1961 and 1962). The (240)Pu/(239)Pu ratio ranged from 0.15 to 0.19, and (236)U/(239)Pu ranged from 0.18 to 1.4. The Pu atom ratios ranged within the limits of global fallout in the most intensive period of nuclear atmospheric testing (1952 to 1962). To the best knowledge of the authors the present work is the first publication on biogeochemical cycles with respect to (236)U concentrations and (236)U/(239)Pu atom ratios in the Arctic and in ice cores. Copyright © 2013 Elsevier B.V. All rights reserved.

  5. Simultaneous measurements of plutonium and uranium in spent-fuel dissolver solutions

    Energy Technology Data Exchange (ETDEWEB)

    Li, T.K. [Los Alamos National Lab., NM (United States); Kuno, T.; Kitagawa, O.; Sato, S.; Kurosawa, A.; Kuno, Y. [Power Reactor and Nuclear Fuel Development Corp., Tokai, Ibaraki (Japan)

    1997-11-01

    The authors have studied the isotope dilution gamma-ray spectrometry (IDGS) technique for simultaneous measurements of elemental concentrations and isotopic compositions for both plutonium and uranium in input spent-fuel dissolver solutions at a reprocessing plant. The technique under development includes both sample preparation and analysis methods. For simultaneous measurements of both plutonium and uranium, a critical issue is to develop a new method to keep both plutonium and uranium in the sample after they are separated from fission products. Furthermore, it is equally important to improve the analysis method so that the precision and accuracy of the plutonium analysis remain unaffected while uranium is retained in the sample. To keep both plutonium and uranium in the sample for simultaneous measurements, extraction chromatography is being studied and shows promise to achieve the goal of cosegregation of the plutonium and uranium. The technique uses U/TEVA{center_dot}Spec resin to separate fission products and recover both uranium and plutonium in the resin from dissolver solutions for subsequent measuring using high-resolution gamma-ray spectrometry. Owing to the fact that the U/Pu ratio is altered during the fission product separation phase, it is necessary to develop a method which could accurately correct for this effect. Such a method was developed using the unique decay properties of {sup 241}Pu to {sup 237}U and shows considerable promise in allowing for accurate determination of the {sup 235}U concentrations before the chemical extraction.

  6. Temporal evolution of (137)Cs, (237)Np, and (239+240)Pu and estimated vertical (239+240)Pu export in the northwestern Mediterranean Sea.

    Science.gov (United States)

    Bressac, M; Levy, I; Chamizo, E; La Rosa, J J; Povinec, P P; Gastaud, J; Oregioni, B

    2017-10-01

    The evolution of (137)Cs, (237)Np and (239+240)Pu at the DYFAMED station (NW Mediterranean) is discussed in relation to physical processes, downward fluxes of particles, and changes in the main input sources. The data set presented in this study represents the first complete (237)Np vertical profiles (0.12-0.27μBqL(-1)), and constitutes a baseline measurement to assess future changes. A similar behavior of Cs and Np has been evidenced, confirming that Np behaves conservatively. While the (137)Cs decrease has been driven by its radioactive decay, the vertical distribution of (237)Np has not substantially changed over the last decade. In the absence of recent major inputs, a homogenization of their vertical distribution occurred, partly due to deep convection events that became more intense during the last decade. In contrast, (239+240)Pu surface levels in the NW Mediterranean waters have fallen in the past four decades by a factor of 5. This decrease in surface has been balanced by higher concentrations in the deep-water layers. A first estimate of the downward (239+240)Pu fluxes in the NW Mediterranean Sea is proposed over more than two decades. This estimation, based on the DYFAMED sediment trap time-series data and published (239+240)Pu flux measurements, suggests that sinking particles have accounted for 60-90% of the upper layer (0-200m) Pu inventory loss over the period 1989-2013. The upper layer residence time of Pu is estimated to be ~28years, twice as long as the residence time estimated for the whole western Mediterranean (~15years). This difference highlights the slow removal of Pu in the open waters of the NW Mediterranean and confirms that most of the Pu removal occurs along the coastal margin where sedimentation rates are high. Copyright © 2017 Elsevier B.V. All rights reserved.

  7. ZPR-6 assembly 7 high {sup 240}Pu core experiments : a fast reactor core with mixed (Pu,U)-oxide fuel and a centeral high{sup 240}Pu zone.

    Energy Technology Data Exchange (ETDEWEB)

    Lell, R. M.; Morman, J. A.; Schaefer, R.W.; McKnight, R.D.; Nuclear Engineering Division

    2009-02-23

    ZPR-6 Assembly 7 (ZPR-6/7) encompasses a series of experiments performed at the ZPR-6 facility at Argonne National Laboratory in 1970 and 1971 as part of the Demonstration Reactor Benchmark Program (Reference 1). Assembly 7 simulated a large sodium-cooled LMFBR with mixed oxide fuel, depleted uranium radial and axial blankets, and a core H/D near unity. ZPR-6/7 was designed to test fast reactor physics data and methods, so configurations in the Assembly 7 program were as simple as possible in terms of geometry and composition. ZPR-6/7 had a very uniform core assembled from small plates of depleted uranium, sodium, iron oxide, U{sub 3}O{sub 8} and Pu-U-Mo alloy loaded into stainless steel drawers. The steel drawers were placed in square stainless steel tubes in the two halves of a split table machine. ZPR-6/7 had a simple, symmetric core unit cell whose neutronic characteristics were dominated by plutonium and {sup 238}U. The core was surrounded by thick radial and axial regions of depleted uranium to simulate radial and axial blankets and to isolate the core from the surrounding room. The ZPR-6/7 program encompassed 139 separate core loadings which include the initial approach to critical and all subsequent core loading changes required to perform specific experiments and measurements. In this context a loading refers to a particular configuration of fueled drawers, radial blanket drawers and experimental equipment (if present) in the matrix of steel tubes. Two principal core configurations were established. The uniform core (Loadings 1-84) had a relatively uniform core composition. The high {sup 240}Pu core (Loadings 85-139) was a variant on the uniform core. The plutonium in the Pu-U-Mo fuel plates in the uniform core contains 11% {sup 240}Pu. In the high {sup 240}Pu core, all Pu-U-Mo plates in the inner core region (central 61 matrix locations per half of the split table machine) were replaced by Pu-U-Mo plates containing 27% {sup 240}Pu in the plutonium

  8. Neutron-induced transmutation reactions in 237Np, 238Pu, and 239Pu at the massive natural uranium spallation target

    Science.gov (United States)

    Zavorka, L.; Adam, J.; Baldin, A. A.; Caloun, P.; Chilap, V. V.; Furman, W. I.; Kadykov, M. G.; Khushvaktov, J.; Pronskikh, V. S.; Solnyshkin, A. A.; Sotnikov, V.; Stegailov, V. I.; Suchopar, M.; Tsoupko-Sitnikov, V. M.; Tyutyunnikov, S. I.; Voronko, V.; Vrzalova, J.

    2015-04-01

    Transmutation reactions in the 237Np, 238Pu, and 239Pu samples were investigated in the neutron field generated inside a massive (m = 512 kg) natural uranium spallation target. The uranium target assembly QUINTA was irradiated with the deuteron beams of kinetic energy 2, 4, and 8 GeV provided by the Nuclotron accelerator at the Joint Institute for Nuclear Research (JINR) in Dubna. The neutron-induced transmutation of the actinide samples was measured off-line by implementing methods of gamma-ray spectrometry with HPGe detectors. Results of measurement are expressed in the form of both the individual reaction rates and average fission transmutation rates. For the purpose of validation of radiation transport programs, the experimental results were compared with simulations of neutron production and distribution performed by the MCNPX 2.7 and MARS15 codes employing the INCL4-ABLA physics models and LAQGSM event generator, respectively. In general, a good agreement between the experimental and calculated reaction rates was found in the whole interval of provided beam energies.

  9. Feasibility study of U-235, Pu-239 and Pu-240 content determination in an irradiated fuel by neutron transmission analysis

    Energy Technology Data Exchange (ETDEWEB)

    Naguib, K.; Michaiel, M.L.; Morcos, H.N

    1998-07-01

    A proposed nondestructive method and its feasibility for the determination of U-235, Pu-239 and Pu-240 contents in an irradiated fuel is described. The method is based on the use of shape fit analysis of the Time-Of-Flight (TOF) neutron transmission data of the irradiated fuel for neutron energies below 3 eV. The neutron transmission experiment of the irradiated fuel is planned to carry out using one of the TOF spectrometers installed at ET-RR-1 reactor. The computer code SHAPE is adapted taking into account the known parameters of resonances of certain fissile and fission product nuclei to provide the fit analysis. The content of the gross-fissile and fission product isotopes are determined from the burn-up calculations of the fuel assembly of the ET-RR-1 reactor with defined history. The effect of both uncertainties in resonance parameters on the deduced contents of fissile nuclei and statistical accuracy of the TOF measurements are estimated.

  10. Pu isotopes in soils collected downwind from Lop Nor: regional fallout vs. global fallout

    Science.gov (United States)

    Bu, Wenting; Ni, Youyi; Guo, Qiuju; Zheng, Jian; Uchida, Shigeo

    2015-07-01

    For the first time, soil core samples from the Jiuquan region have been analyzed for Pu isotopes for radioactive source identification and radiological assessment. The Jiuquan region is in downwind from the Lop Nor Chinese nuclear test (CNT) site. The high Pu inventories (13 to 546 Bq/m2) in most of the sampling locations revealed that this region was heterogeneously contaminated by the regional fallout Pu from the CNTs. The contributions of the CNTs to the total Pu in soils were estimated to be more than 40% in most cases. The 240Pu/239Pu atom ratios in the soils ranged from 0.059 to 0.186 with an inventory-weighted average of 0.158, slightly lower than that of global fallout. This atom ratio could be considered as a mixed fingerprint of Pu from the CNTs. In addition, Pu in soils of Jiuquan region had a faster downward migration rate compared with other investigated places in China.

  11. Commitment to the monocytic lineage occurs in the absence of the transcription factor PU.1.

    NARCIS (Netherlands)

    G.W. Henkel; S.R. McKercher; P.J. Leenen (Pieter); R.A. Maki

    1999-01-01

    textabstractMice homozygous for the disruption of the PU.1 (Spi-1) gene do not produce mature macrophages. In determining the role of PU.1 in macrophage differentiation, the present study investigated whether or not there was commitment to the monocytic lineage in the a

  12. {sup 241}Pu concentrations in water, plankton and fish from the southern Baltic Sea

    Energy Technology Data Exchange (ETDEWEB)

    Struminska-Parulska, D.I.; Skwarzec, B. [Gdansk, Univ. (Poland). Facuty of Chemistry

    2013-08-01

    The aim of the work was to determine {sup 241}Pu activities in different components (water, plankton and fish) of the southern Baltic Sea ecosystem. Measurement of {sup 241}Pu in the samples was done indirectly by determining the increment in {sup 241}Am from the decay of the {beta}-emitting {sup 241}Pu in samples collected 10-15 years after the Chernobyl accident. Enhanced levels of {sup 241}Pu were observed in all analyzed Baltic samples. The highest {sup 241}Pu concentrations in fish were found in Perciformes: benthic round goby (0.863 {+-} 0.066 mBq/g ww) and pelagic perch (0.666 {+-} 0.001 mBq/g ww). Plutonium is also non-uniformly distributed in the organs and tissues of the analyzed fish; especially pelagic herring and cod as well as benthic flounder. Most of {sup 241}Pu in flounder, herring and cod is located in soft tissues, especially digestive organs (stomach, intestine, liver). The annual individual effective doses calculated on the basis of {sup 241}Pu concentrations in fish indicated that the impact of the consumption of {sup 241}Pu containing Baltic fish on the annual effective dose for a statistical inhabitant of Poland was very small. (orig.)

  13. PU.1 cooperates with IRF4 and IRF8 to suppress pre-B-cell leukemia.

    Science.gov (United States)

    Pang, S H M; Minnich, M; Gangatirkar, P; Zheng, Z; Ebert, A; Song, G; Dickins, R A; Corcoran, L M; Mullighan, C G; Busslinger, M; Huntington, N D; Nutt, S L; Carotta, S

    2016-06-01

    The Ets family transcription factor PU.1 and the interferon regulatory factor (IRF)4 and IRF8 regulate gene expression by binding to composite DNA sequences known as Ets/interferon consensus elements. Although all three factors are expressed from the onset of B-cell development, single deficiency of these factors in B-cell progenitors only mildly impacts on bone marrow B lymphopoiesis. Here we tested whether PU.1 cooperates with IRF factors in regulating early B-cell development. Lack of PU.1 and IRF4 resulted in a partial block in development the pre-B-cell stage. The combined deletion of PU.1 and IRF8 reduced recirculating B-cell numbers. Strikingly, all PU.1/IRF4 and ~50% of PU.1/IRF8 double deficient mice developed pre-B-cell acute lymphoblastic leukemia (B-ALL) associated with reduced expression of the established B-lineage tumor suppressor genes, Ikaros and Spi-B. These genes are directly regulated by PU.1/IRF4/IRF8, and restoration of Ikaros or Spi-B expression inhibited leukemic cell growth. In summary, we demonstrate that PU.1, IRF4 and IRF8 cooperate to regulate early B-cell development and to prevent pre-B-ALL formation.

  14. Pu isotopes in soils collected downwind from Lop Nor: regional fallout vs. global fallout.

    Science.gov (United States)

    Bu, Wenting; Ni, Youyi; Guo, Qiuju; Zheng, Jian; Uchida, Shigeo

    2015-07-17

    For the first time, soil core samples from the Jiuquan region have been analyzed for Pu isotopes for radioactive source identification and radiological assessment. The Jiuquan region is in downwind from the Lop Nor Chinese nuclear test (CNT) site. The high Pu inventories (13 to 546 Bq/m(2)) in most of the sampling locations revealed that this region was heterogeneously contaminated by the regional fallout Pu from the CNTs. The contributions of the CNTs to the total Pu in soils were estimated to be more than 40% in most cases. The (240)Pu/(239)Pu atom ratios in the soils ranged from 0.059 to 0.186 with an inventory-weighted average of 0.158, slightly lower than that of global fallout. This atom ratio could be considered as a mixed fingerprint of Pu from the CNTs. In addition, Pu in soils of Jiuquan region had a faster downward migration rate compared with other investigated places in China.

  15. Radiation chemical behavior of actinides in extraction systems. IV. Interaction of Pu(IV) with H/sub 3/PO/sub 4/ in the system 30% TBP + n-dodecane

    Energy Technology Data Exchange (ETDEWEB)

    Fedoseev, D.A.; Boikova, I.A.; Milovanova, A.S.; Fedotov, S.N.; Naumov, M.A.; Vladimirova, M.V.

    1987-05-01

    Spectrophotometric, radiometric (..gamma..-spectrophotometric), and elemental analyses were used to determine the composition, solubility, and concentration stability constant K of complexes of Pu(IV) with H/sub 3/PO/sub 4/ in the system 30% TBP + n-dodecane containing 0.45 M HNO/sub 3/. For a Pu(IV) concentration of approx. 1 x 10/sup -2/ M and a molar concentration ratio of H/sub 3/PO/sub 4/ and Pu(IV) of less than or equal to 2.5 the sparingly soluble (1.8 x 10/sup -3/ M) complex Pu(HPO/sub 4/)/sub 2/ is formed. In the range of H/sub 3/PO/sub 4/ concentrations (C/sub L//sup 0/) from 5 x 10/sup -3/ to 3.0 x 10/sup -2/ M the value of K does not depend on C/sub L//sup 0/ and is (1.8 +/- 0.6) x 10/sup 5/ liter/sup 2//mole/sup 2/. The results are discussed and compared with the interaction of Pu(IV) with DBPA and MBPA in aqueous and organic solutions.

  16. The production of {sup 238-242}Pu(n,γ){sup 239-243}Pu fissionable fluids in a fusion-fission hybrid reactor

    Energy Technology Data Exchange (ETDEWEB)

    Guenay, Mehtap [Inoenue Univ., Malatya (Turkey). Physics Dept.

    2014-03-15

    In this study, the effect of spent fuel grade plutonium content on {sup 239-243}Pu was investigated in a designed hybrid reactor system. In this system, the fluids were composed of a molten salt, heavy metal mixture with increased mole fractions 99-95 % Li{sub 20}Sn{sub 80}-1-5 % SFG-Pu, 99-95 % Li{sub 20}Sn{sub 80}-1-5 % SFG-PuF{sub 4}, 99-95 % Li{sub 20}Sn{sub 80}-1-5 % SFG-PuO{sub 2}. Beryllium (Be) is a neutron multiplier by (n,2n) reactions. Thence, a Be zone of 3 cm thickness was used in order to contribute to fissile fuel breeding between the liquid first wall and a 9Cr2WVTa ferritic steel blanket which is used as structural material. The production of {sup 238-242}Pu(n,γ){sup 239-243}Pu was calculated in liquid first wall, blanket and shielding zones. Three-dimensional nucleonic calculations were performed by using the most recent version MCNPX-2.7.0 Monte Carlo code and nuclear data library ENDF/B-VII.0. (orig.)

  17. Chronology of Pu isotopes and {sup 236}U in an Arctic ice core

    Energy Technology Data Exchange (ETDEWEB)

    Wendel, C.C., E-mail: cato.wendel@umb.no [Isotope Laboratory, Department of Plant and Environmental Sciences, Agricultural University of Norway, P.O. Box 5003, N-1432 Aas (Norway); Oughton, D.H., E-mail: deborah.oughton@umb.no [Isotope Laboratory, Department of Plant and Environmental Sciences, Agricultural University of Norway, P.O. Box 5003, N-1432 Aas (Norway); Lind, O.C., E-mail: ole-christian.lind@umb.no [Isotope Laboratory, Department of Plant and Environmental Sciences, Agricultural University of Norway, P.O. Box 5003, N-1432 Aas (Norway); Skipperud, L., E-mail: lindis.skipperud@umb.no [Isotope Laboratory, Department of Plant and Environmental Sciences, Agricultural University of Norway, P.O. Box 5003, N-1432 Aas (Norway); Fifield, L.K., E-mail: keith.fifield@anu.edu.au [Department of Nuclear Physics, Australian National University, Canberra ACT 0200 (Australia); Isaksson, E., E-mail: elisabeth.isaksson@npolar.no [Norwegian Polar Institute, Fram Centre, Hjalmar Johansens Gate 14, N9296 Tromsø (Norway); Tims, S.G., E-mail: steve.tims@anu.edu.au [Department of Nuclear Physics, Australian National University, Canberra ACT 0200 (Australia); Salbu, B., E-mail: brit.salbu@umb.no [Isotope Laboratory, Department of Plant and Environmental Sciences, Agricultural University of Norway, P.O. Box 5003, N-1432 Aas (Norway)

    2013-09-01

    In the present work, state of the art isotopic fingerprinting techniques are applied to an Arctic ice core in order to quantify deposition of U and Pu, and to identify possible tropospheric transport of debris from former Soviet Union test sites Semipalatinsk (Central Asia) and Novaya Zemlya (Arctic Ocean). An ice core chronology of {sup 236}U, {sup 239}Pu, and {sup 240}Pu concentrations, and atom ratios, measured by accelerator mass spectrometry in a 28.6 m deep ice core from the Austfonna glacier at Nordaustlandet, Svalbard is presented. The ice core chronology corresponds to the period 1949 to 1999. The main sources of Pu and {sup 236}U contamination in the Arctic were the atmospheric nuclear detonations in the period 1945 to 1980, as global fallout, and tropospheric fallout from the former Soviet Union test sites Novaya Zemlya and Semipalatinsk. Activity concentrations of {sup 239+240}Pu ranged from 0.008 to 0.254 mBq cm{sup −2} and {sup 236}U from 0.0039 to 0.053 μBq cm{sup −2}. Concentrations varied in concordance with {sup 137}Cs concentrations in the same ice core. In contrast to previous published results, the concentrations of Pu and {sup 236}U were found to be higher at depths corresponding to the pre-moratorium period (1949 to 1959) than to the post-moratorium period (1961 and 1962). The {sup 240}Pu/{sup 239}Pu ratio ranged from 0.15 to 0.19, and {sup 236}U/{sup 239}Pu ranged from 0.18 to 1.4. The Pu atom ratios ranged within the limits of global fallout in the most intensive period of nuclear atmospheric testing (1952 to 1962). To the best knowledge of the authors the present work is the first publication on biogeochemical cycles with respect to {sup 236}U concentrations and {sup 236}U/{sup 239}Pu atom ratios in the Arctic and in ice cores. - Highlights: • Concentrations and atom ratios of Pu and {sup 236}U determined in an Arctic ice core. • Concentrations of U and Pu found to be higher pre- than post-moratorium. • U and Pu concentrations

  18. Alpha and conversion electron spectroscopy of 238,239Pu and 241Am and alpha-conversion electron coincidence measurements

    Science.gov (United States)

    Dion, Michael P.; Miller, Brian W.; Warren, Glen A.

    2016-09-01

    A technique to determine the isotopic constituents of a mixed actinide sample has been proposed by a coincident alpha-conversion electron measurement. This presents a unique signature to allow the unfolding of isotopes that possess overlapping alpha particle energy and reduce backgrounds of an unseparated sample. The work presented here are results of conversion electron spectroscopy of 241Am, 238Pu and 239Pu using a dual-stage peltier-cooled 25 mm2 silicon drift detector and alpha spectroscopy with a passivated ion implanted planar silicon detector. The conversion electron spectra were evaluated from 20-55 keV based on fits to the dominant conversion electron emissions, which allowed the relative conversion electron emission intensities to be determined. These measurements provide crucial singles spectral information and calibration to aid in the coincident measurement approach. Furthermore, an alpha-conversion electron spectrometer was assembled using the silicon based detectors described and results of a coincident spectrum analysis is reported for 241Am.

  19. AMS of actinides in groundwater: development of a new procedure for trace analysis of Np, Pu, Am and Cm isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Quinto, Francesca; Lagos, Markus; Plaschke, Markus; Schaefer, Thorsten; Geckeis, Horst [Karlsruhe Institute of Technology, Institute for Nuclear Waste Disposal (KIT-INE), Hermann-von Helmholtz-Platz 1, D-76344 Eggenstein-Leopoldshafen (Germany); Steier, Peter [VERA Laboratory, Faculty of Physics, University of Vienna, Waehringer Strasse 17, A-1090 Vienna (Austria)

    2014-07-01

    In order to assess the actinides contamination in groundwater, their geochemistry is intensely studied in field and laboratory experiments focusing on speciation and ways of transport through the aquifers. A challenge lies in the analysis of actinides below ppq levels. We present a new analytical protocol suited to the measurement by accelerator mass spectrometry of Np, Pu, Am and Cm isotopes without previous chemical separation from each other. The actinides are quantitatively co-precipitated with Fe-hydroxide from the groundwater specimens. This procedure allows the pre-concentration of the actinides from the bulk elements and their incorporation into a sample matrix suited to the AMS measurements. The chemical yield of the co-precipitation is estimated measuring samples with suitable spikes by HR ICP-MS. At the AMS sytem: (a) the ionization yield of Np, Pu, Am and Cm in the given sample matrix, (b) the maximum number of nuclides per sample allowing detection limits below 0.01 ppq, and (c) the influence of the laboratory background on the results, are determined.

  20. Effect of Putrescine, 4-PU-30, and Abscisic Acid on Maize Plants Grown under Normal, Drought, and Rewatering Conditions.

    Science.gov (United States)

    Todorov; Alexieva; Karanov

    1998-12-01

    The experiments were carried out with maize (Zea mays L.) seedlings, hybrid Kneja 530, grown hydroponically in a growth chamber. Twelve-day-old plants were foliar treated with putrescine, N1-(2-chloro-4-pyridyl)-N2-phenylurea (4-PU-30), and abscisic acid (ABA) at concentrations of 10(-5) m. Twenty-four hours later the plants were subjected to a water deficit program, induced by 15% polyethylene glycol (PEG; molecular weight, 6,000). Three days after drought stress half of the plants were transferred to nutrient solution for the next 3 days. The effects of the water shortage, rewatering, and plant growth regulator (PGR) treatment on the fresh and dry weights, leaf pigment content, proline level, relative water content (RWC), transpiration rate, activities of catalase and guaiacol peroxidase, hydrogen peroxide content, and level of the products of lipid peroxidation were studied. It was established that the application of PGRs alleviated to some extent the plant damage provoked by PEG stress. At the end of the water shortage program the plants treated with these PGRs possessed higher fresh weight than drought-subjected control seedlings. It was found also that putrescine increased the dry weight of plants. Under drought, the RWC and transpiration rate of seedlings declined, but PGR treatment reduced these effects. The accumulation of free proline, malondialdehyde, and hydrogen peroxide was prevented in PGR-treated plants compared with the water stress control. The results provided further information about the influence of putrescine, 4-PU-30, and ABA on maize plants grown under normal, drought, and rewatering conditions. Key Words. Maize-Putrescine-4-PU-30-ABA-Drought

  1. Synthesis and fluorescence enhancement behavior of a novel fluorescent aqueous polyurethane emulsion DDAQ-TDI-PU

    Institute of Scientific and Technical Information of China (English)

    Xian Hai Hu; Xing Yuan Zhang; Jia Bing Dai

    2012-01-01

    A novel fluorescent aqueous polyurethane emulsion DDAQ-TDI-PU was synthesized by blocking the anthraquinone moiety of 1,4-diamino-2,3-diphenoxyanthraquinone (DDAQ) into polyurethane chain using 2,4-tolylene diisocyanate (TDI),poly(propylene glycol) and 2,2-dimethylol propionic acid.The chain structure of DDAQ-TDI-PU was confirmed by means of Fourier transform infrared spectroscopy and UV-vis analysis.Comparing to the UV-vis spectrum of DDAQ,DDAQ-TDI-PU showed a hypsochromic shift from the absorption maxima of 518,558,609 nm to 510,548,586 nm,respectively.It was found that the fluorescence intensity of DDAQ-TDI-PU emulsion was enhanced greatly comparing with that of DDAQ.The fluorescence of DDAQ-TDI-PU was very stable not only for the long term storage but also for the fluorescence quencher.

  2. AMS of natural {sup 236}U and {sup 239}Pu produced in uranium ores

    Energy Technology Data Exchange (ETDEWEB)

    Wilcken, K.M. [Department of Nuclear Physics, RSPhysSE, Australian National University, Canberra, ACT 0200 (Australia)]. E-mail: k.wilcken@suerc.gla.ac.uk; Barrows, T.T. [Department of Nuclear Physics, RSPhysSE, Australian National University, Canberra, ACT 0200 (Australia); Fifield, L.K. [Department of Nuclear Physics, RSPhysSE, Australian National University, Canberra, ACT 0200 (Australia); Tims, S.G. [Department of Nuclear Physics, RSPhysSE, Australian National University, Canberra, ACT 0200 (Australia); Steier, P. [VERA Laboratory, Institute for Isotopic Research and Nuclear Physics, University of Vienna, Waehringer Strasse 17, A-1090 Vienna (Austria)

    2007-06-15

    The rare isotopes {sup 236}U and {sup 239}Pu are produced naturally by neutron capture in uranium ores. Here we measure {sup 236}U and {sup 239}Pu by accelerator mass spectrometry (AMS) in the same ore samples for the first time. To ensure efficient extraction of both elements and isotopic equilibrium between the {sup 239}Pu in the ore and a {sup 242}Pu spike, we developed a new sample preparation protocol. AMS has clear advantages over previous methods because it achieves better discrimination against molecular interferences with higher sensitivity and shorter counting times. Measurements of {sup 236}U and {sup 239}Pu hold considerable promise as proxy indicators of neutron flux and uranium concentration.

  3. Utjecaj pušenja na razvoj i progresiju parodontne bolesti

    OpenAIRE

    Jindra, Lj.; Cindrić, G.; Girotto, M

    2003-01-01

    Pušenje se smatra rizičnim čimbenikom za nastanak i progresiju parodontne bolesti. Svrha je rada bila odrediti prevalenciju pušenja u uzorku ispitivanih pacijenata koji boluju od parodontitisa, utvrditi utjecaj pušenja na razvoj i progresiju parodontne bolesti i usporediti parodontni status pušača i nepušača. Ispitano je dvjesto pacijenata, pola kojih je bilo pušača a pola nepušača, te su podijeljeni u četiri dobne skupine: do 19, 20-35, 35 65 i 66 i više, i klasificirani prema spolu. P...

  4. U.S.-Russian experts NATO collaborative research grant exchange visit meeting on excess Pu ceramics formulations and characterizations

    Energy Technology Data Exchange (ETDEWEB)

    Jardine, L.J., LLNL

    1998-11-24

    This document contains the agenda and meeting notes. Topics of discussion included US Pu disposition ceramics activities, Russian experience and proposals in Pu ceramics, and development of possible Russian ceramic proposals or collaborations.

  5. Study of the effect of (U{sub 0.8}Pu{sub 0.2})O{sub 2} Uranium-Plutonium mixed fuel fission products on a living organism

    Energy Technology Data Exchange (ETDEWEB)

    Baimukhanova, Ayagoz; Kim, Dmitriy [Dept. of Radiation Protection, Institute of Nuclear Physics of the Ministry of Energy of the Republic of Kazakhstan, Almaty (Kazakhstan); Zhumagulova, Roza; Tazhigulova, Bibnur; Zharaspayeva, Gulzhanar; Azhiyeva, Galiya [Faculty of Engineering Technologies, Infrastructure and Management, International Educational Corporation, Almaty (Kazakhstan)

    2016-08-15

    The article describes the results of experiments conducted on pigs to determine the effect of plutonium, which is the most radiotoxic and highly active element in the range of mixed fuel (U{sub 0.8}Pu{sub 0.2})O{sub 2} fission products, on living organisms. The results will allow empirical prediction of the emergency plutonium radiation dose for various organs and tissues of humans in case of an accident in a reactor running on mixed fuel (U{sub 0.8}Pu{sub 0.2})O{sub 2}.

  6. A self-consistent DFT + DMFT scheme in the projector augmented wave method: applications to cerium, Ce2O3 and Pu2O3 with the Hubbard I solver and comparison to DFT + U.

    Science.gov (United States)

    Amadon, B

    2012-02-22

    An implementation of full self-consistency over the electronic density in the DFT + DMFT framework on the basis of a plane wave–projector augmented wave (PAW) DFT code is presented. It allows for an accurate calculation of the total energy in DFT + DMFT within a plane wave approach. In contrast to frameworks based on the maximally localized Wannier function, the method is easily applied to f electron systems, such as cerium, cerium oxide (Ce2O3) and plutonium oxide (Pu2O3). In order to have a correct and physical calculation of the energy terms, we find that the calculation of the self-consistent density is mandatory. The formalism is general and does not depend on the method used to solve the impurity model. Calculations are carried out within the Hubbard I approximation, which is fast to solve, and gives a good description of strongly correlated insulators. We compare the DFT + DMFT and DFT + U solutions, and underline the qualitative differences of their converged densities. We emphasize that in contrast to DFT + U, DFT + DMFT does not break the spin and orbital symmetry. As a consequence, DFT + DMFT implies, on top of a better physical description of correlated metals and insulators, a reduced occurrence of unphysical metastable solutions in correlated insulators in comparison to DFT + U.

  7. Distribution of Np and Pu in Swedish lichen samples (Cladonia stellaris) contaminated by atmospheric fallout

    Energy Technology Data Exchange (ETDEWEB)

    Lindahl, Patric E-mail: patric.lindahl@radfys.lu.se; Roos, Per; Eriksson, Mats; Holm, Elis

    2004-07-01

    The activity concentrations of {sup 237}Np and the two Pu isotopes, {sup 239}Pu and {sup 240}Pu, were determined in lichen samples (Cladonia stellaris) contaminated by fallout from atmospheric nuclear test explosions and the Chernobyl accident. The samples were collected at 18 locations in Sweden, from north to south, between 1986 and 1988 and analysed with high-resolution inductively coupled plasma mass spectrometry (HR-ICP-MS) and alpha spectrometry. Data on the activity ratios {sup 238}Pu/{sup 239+240}Pu and {sup 134}Cs/{sup 137}Cs measured previously were also included in this study for comparison. The {sup 237}Np activity concentration ranged from 0.08{+-}0.01 to 2.08{+-}0.17 mBq kg{sup -1}, depending on the location of the sampling site and time of collection. The {sup 239+240}Pu activity concentration ranged from 0.09{+-}0.01 to 4.09{+-}0.15 Bq kg{sup -1}, with the {sup 240}Pu/{sup 239}Pu atomic ratio ranging between 0.16{+-}0.01 and 0.44{+-}0.03, the higher ratios indicating a combination of weapons test fallout and Chernobyl fallout. The {sup 237}Np/{sup 239}Pu atomic ratios ranged between 0.06{+-}0.01 and 0.42{+-}0.04, the lower ratios indicating combination of weapons test fallout and Chernobyl fallout. At a well-defined sampling site at Lake Rogen (62.32 deg. N, 12.38 deg. E), additional lichen samples were collected between 1987 and 1998 to study the distribution of Np and Pu in different layers. The concentrations of the two elements follow each other quite well in the profile.

  8. Nrf2 regulates PU.1 expression and activity in the alveolar macrophage.

    Science.gov (United States)

    Staitieh, Bashar S; Fan, Xian; Neveu, Wendy; Guidot, David M

    2015-05-15

    Alveolar macrophage (AM) immune function depends on the activation of the transcription factor PU.1 by granulocyte macrophage colony-stimulating factor. We have determined that chronic alcohol ingestion dampens PU.1 signaling via an unknown zinc-dependent mechanism; specifically, although PU.1 is not known to be a zinc-dependent transcription factor, zinc treatment reversed alcohol-mediated dampening of PU.1 signaling. Nuclear factor (erythroid-derived 2)-like 2 (Nrf2), a zinc-dependent basic leucine zipper protein essential for antioxidant defenses, is also impaired by chronic alcohol ingestion and enhanced by zinc treatment. We hypothesized that the response of PU.1 to zinc treatment may result from the action of Nrf2 on PU.1. We first performed Nrf2/PU.1 protein coimmunoprecipitation on a rat AM cell line (NR8383) and found no evidence of protein-protein interactions. We then found evidence of increased Nrf2 binding to the PU.1 promoter region by chromatin immunoprecipitation. We next activated Nrf2 using either sulforaphane or an overexpression vector and inhibited Nrf2 with silencing RNA to determine whether Nrf2 could actively regulate PU.1. Nrf2 activation increased protein expression of both factors as well as gene expression of their respective downstream effectors, NAD(P)H dehydrogenase[quinone] 1 (NQO1) and cluster of differentiation antigen-14 (CD14). In contrast, Nrf2 silencing decreased the expression of both proteins, as well as gene expression of their effectors. Activating and inhibiting Nrf2 in primary rat AMs resulted in similar effects. Taken together, these findings suggest that Nrf2 regulates the expression and activity of PU.1 and that antioxidant response and immune activation are coordinately regulated within the AM.

  9. Thermodynamic assessment of the LiF–ThF4–PuF3–UF4 system

    NARCIS (Netherlands)

    Capelli, E.; Benes, O.; Konings, R.J.M.

    2015-01-01

    The LiF–ThF4–PuF3–UF4 system is the reference salt mixture considered for the Molten Salt Fast Reactor (MSFR) concept started with PuF3. In order to obtain the complete thermodynamic description of this quaternary system, two binary systems (ThF4–PuF3 and UF4–PuF3) and two ternary systems (LiF–ThF4–

  10. {sup 137}Cs, {sup 239+240}Pu and {sup 240}Pu/{sup 239}Pu atom ratios in the surface waters of the western North Pacific Ocean, eastern Indian Ocean and their adjacent seas

    Energy Technology Data Exchange (ETDEWEB)

    Yamada, Masatoshi; Zheng, Jian; Wang, Zhong-Liang [Nakaminato Laboratory for Marine Radioecology, National Institute of Radiological Sciences, Isozaki 3609, Hitachinaka, Ibaraki 311-1202 (Japan)

    2006-07-31

    Surface seawater samples were collected along the track of the R/V Hakuho-Maru cruise (KH-96-5) from Tokyo to the Southern Ocean. The {sup 137}Cs activities were determined for the surface waters in the western North Pacific Ocean, the Sulu and Indonesian Seas, the eastern Indian Ocean, the Bay of Bengal, the Andaman Sea, and the South China Sea. The {sup 137}Cs activities showed a wide variation with values ranging from 1.1 Bq m{sup -3} in the Antarctic Circumpolar Region of the Southern Ocean to 3 Bq m{sup -3} in the western North Pacific Ocean and the South China Sea. The latitudinal distributions of {sup 137}Cs activity were not reflective of that of the integrated deposition density of atmospheric global fallout. The removal rates of {sup 137}Cs from the surface waters were roughly estimated from the two data sets of Miyake et al. [Miyake Y, Saruhashi K, Sugimura Y, Kanazawa T, Hirose K. Contents of {sup 137}Cs, plutonium and americium isotopes in the Southern Ocean waters. Pap Meteorol Geophys 1988;39:95-113] and this study to be 0.016 yr{sup -1} in the Sulu and Indonesian Seas, 0.033 yr{sup -1} in the Bay of Bengal and Andaman Sea, and 0.029 yr{sup -1} in the South China Sea. These values were much lower than that in the coastal surface water of the western Northwest Pacific Ocean. This was likely due to less horizontal and vertical mixing of water masses and less scavenging. {sup 239+240}Pu activities and {sup 240}Pu/{sup 239}Pu atom ratios were also determined for the surface waters in the western North Pacific Ocean, the Sulu and Indonesian Seas and the South China Sea. The {sup 240}Pu/{sup 239}Pu atom ratios ranged from 0.199+/-0.026 to 0.248+/-0.027 on average, and were significantly higher than the global stratospheric fallout ratio of 0.18. The contributions of the North Pacific Proving Grounds close-in fallout Pu were estimated to be 20% for the western North Pacific Ocean, 39% for the Sulu and Indonesian Seas and 42% for the South China Sea by using

  11. {sup 137}Cs, {sup 239+24}Pu and {sup 24}Pu/{sup 239}Pu atom ratios in the surface waters of the western North Pacific Ocean, eastern Indian Ocean and their adjacent seas

    Energy Technology Data Exchange (ETDEWEB)

    Yamada, Masatoshi [Nakaminato Laboratory for Marine Radioecology, National Institute of Radiological Sciences, Isozaki 3609, Hitachinaka, Ibaraki 311-1202 (Japan)]. E-mail: m_yamada@nirs.go.jp; Zheng Jian [Nakaminato Laboratory for Marine Radioecology, National Institute of Radiological Sciences, Isozaki 3609, Hitachinaka, Ibaraki 311-1202 (Japan); Wang Zhongliang [Nakaminato Laboratory for Marine Radioecology, National Institute of Radiological Sciences, Isozaki 3609, Hitachinaka, Ibaraki 311-1202 (Japan); State Key Laboratory of Environmental Geochemistry, Institute of Geochemistry, Chinese Academy of Sciences, Guanshui Road 46, Guiyang 550002 (China)

    2006-07-31

    Surface seawater samples were collected along the track of the R/V Hakuho-Maru cruise (KH-96-5) from Tokyo to the Southern Ocean. The {sup 137}Cs activities were determined for the surface waters in the western North Pacific Ocean, the Sulu and Indonesian Seas, the eastern Indian Ocean, the Bay of Bengal, the Andaman Sea, and the South China Sea. The {sup 137}Cs activities showed a wide variation with values ranging from 1.1 Bq m{sup -3} in the Antarctic Circumpolar Region of the Southern Ocean to 3 Bq m{sup -3} in the western North Pacific Ocean and the South China Sea. The latitudinal distributions of {sup 137}Cs activity were not reflective of that of the integrated deposition density of atmospheric global fallout. The removal rates of {sup 137}Cs from the surface waters were roughly estimated from the two data sets of Miyake et al. [Miyake Y, Saruhashi K, Sugimura Y, Kanazawa T, Hirose K. Contents of {sup 137}Cs, plutonium and americium isotopes in the Southern Ocean waters. Pap Meteorol Geophys 1988;39:95-113] and this study to be 0.016 yr{sup -1} in the Sulu and Indonesian Seas, 0.033 yr{sup -1} in the Bay of Bengal and Andaman Sea, and 0.029 yr{sup -1} in the South China Sea. These values were much lower than that in the coastal surface water of the western Northwest Pacific Ocean. This was likely due to less horizontal and vertical mixing of water masses and less scavenging. {sup 239+24}Pu activities and {sup 24}Pu/{sup 239}Pu atom ratios were also determined for the surface waters in the western North Pacific Ocean, the Sulu and Indonesian Seas and the South China Sea. The {sup 24}Pu / {sup 239}Pu atom ratios ranged from 0.199 {+-} 0.026 to 0.248 {+-} 0.027 on average, and were significantly higher than the global stratospheric fallout ratio of 0.18. The contributions of the North Pacific Proving Grounds close-in fallout Pu were estimated to be 20% for the western North Pacific Ocean, 39% for the Sulu and Indonesian Seas and 42% for the South China Sea by

  12. Rational Ligand Design for U(VI) and Pu(IV)

    Energy Technology Data Exchange (ETDEWEB)

    Szigethy, Geza [Univ. of California, Berkeley, CA (United States)

    2009-08-12

    Nuclear power is an attractive alternative to hydrocarbon-based energy production at a time when moving away from carbon-producing processes is widely accepted as a significant developmental need. Hence, the radioactive actinide power sources for this industry are necessarily becoming more widespread, which is accompanied by the increased risk of exposure to both biological and environmental systems. This, in turn, requires the development of technology designed to remove such radioactive threats efficiently and selectively from contaminated material, whether that be contained nuclear waste streams or the human body. Raymond and coworkers (University of California, Berkeley) have for decades investigated the interaction of biologically-inspired, hard Lewis-base ligands with high-valent, early-actinide cations. It has been established that such ligands bind strongly to the hard Lewis-acidic early actinides, and many poly-bidentate ligands have been developed and shown to be effective chelators of actinide contaminants in vivo. Work reported herein explores the effect of ligand geometry on the linear U(IV) dioxo dication (uranyl, UO2 2+). The goal is to utilize rational ligand design to develop ligands that exhibit shape selectivity towards linear dioxo cations and provides thermodynamically favorable binding interactions. The uranyl complexes with a series of tetradentate 3-hydroxy-pyridin-2-one (3,2-HOPO) ligands were studied in both the crystalline state as well as in solution. Despite significant geometric differences, the uranyl affinities of these ligands vary only slightly but are better than DTPA, the only FDA-approved chelation therapy for actinide contamination. The terepthalamide (TAM) moiety was combined into tris-beidentate ligands with 1,2- and 3,2-HOPO moieties were combined into hexadentate ligands whose structural preferences and solution thermodynamics were measured with the uranyl cation. In addition to achieving coordinative

  13. Gamma-ray Output Spectra from 239Pu Fission

    Directory of Open Access Journals (Sweden)

    Ullmann John

    2015-01-01

    Full Text Available Gamma-ray multiplicities, individual gamma-ray energy spectra, and total gamma energy spectra following neutron-induced fission of 239Pu were measured using the DANCE detector at Los Alamos. Corrections for detector response were made using a forward-modeling technique based on propagating sets of gamma rays generated from a paramaterized model through a GEANT model of the DANCE array and adjusting the parameters for best fit to the measured spectra. The results for the gamma-ray spectrum and multiplicity are in general agreement with previous results, but the measured total gamma-ray energy is about 10% higher. A dependence of the gamma-ray spectrum on the gamma-ray multplicity was also observed. Global model calculations of the multiplicity and gamma energy distributions are in good agreement with the data, but predict a slightly softer total-energy distribution.

  14. Electronic structure of nitrides PuN and UN

    Energy Technology Data Exchange (ETDEWEB)

    Lukoyanov, A. V., E-mail: lukoyanov@imp.uran.ru; Anisimov, V. I. [Russian Academy of Sciences, Mikheev Institute of Metal Physics, Ural Branch (Russian Federation)

    2016-11-15

    The electronic structure of uranium and plutonium nitrides in ambient conditions and under pressure is investigated using the LDA + U + SO band method taking into account the spin–orbit coupling and the strong correlations of 5f electrons of actinoid ions. The parameters of these interactions for the equilibrium cubic structure are calculated additionally. The application of pressure reduces the magnetic moment in PuN due to predominance of the f{sup 6} configuration and the jj-type coupling. An increase in the occupancy of the 5f state in UN leads to a decrease in the magnetic moment, which is also detected in the trigonal structure of the UN{sub x} β phase (La{sub 2}O{sub 3}-type structure). The theoretical results are in good agreement with the available experimental data.

  15. Helium release from 238PuO2 fuel particles

    Science.gov (United States)

    El-Genk, Mohamed S.; Tournier, Jean-Michel

    2000-01-01

    Coated plutonia fuel particles have recently been proposed for potential use in future space exploration missions that employ radioisotope power systems and/or radioisotope heater units (RHUs). The design of this fuel form calls for full retention of the helium generated by the natural radioactive decay of 238Pu, with the aid of a strong zirconium carbide coating. This paper reviews the potential release mechanisms of helium in small-grain (7-40 μm) plutonia pellets currently being used in the General Purpose Heat Source (GPHS) modules and RHUs, during both steady-state and transient heating conditions. The applicability of these mechanisms to large-grain and polycrystalline 238PuO2 fuel kernels is examined and estimates of helium release during a re-entry heating pulse up to 1723 K are presented. These estimates are based on the reported data for fission gas release from granular and monocrystal UO2 fuel particles irradiated at isothermal conditions up to 6.4 at.% burnup and 2030 K. It is concluded that the helium release fraction from large-grain (>=300 μm) plutonia fuel kernels heated up to 1723 K could be less than 7%, compared to ~80% from small-grain (7-40 μm) fuel. The helium release fraction from polycrystalline plutonia kernels fabricated using Sol-Gel techniques could be even lower. Sol-Gel fabrication processes are favored over powder metallurgy, because of their high precision and excellent reproducibility and the absence of a radioactive dust waste stream, significantly reducing the fabrication and post-fabrication clean-up costs. .

  16. Thermodynamic properties of the cubic plutonium hydride solid solution

    Energy Technology Data Exchange (ETDEWEB)

    Haschke, J M

    1981-12-01

    Pressure, temperature, and composition data for the cubic solid solution plutonium hydride phase, PuH/sub x/, have been measured by microbalance methods. Integral enthalpies and entropies of formation have been evaluated for the composition range 1.90 less than or equal to X less than or equal to 3.00. At 550/sup 0/K, ..delta..H/sup 0/ /sub f/(PuH/sub x/(s)) varies linearly from approximately (-38 +- 1) kcal mol/sup -1/ at PuH/sub 190/ to (-50 +- 1 kcal mol/sup -1/) at PuH/sub 3/ /sub 00/. Thermochemical values obtained by reevaluating tensimetric data from the literature are in excellent agreement with these results. Isotopic effects have been quantified by comparing the results for hydride and deuteride, and equations are presented for predicting ..delta..H/sup 0/ /sub f/ and ..delta..S/sup 0/ /sub f/ values for PuH/sub x/(s) and PuD/sub x/(s).

  17. Plutonium Isotopes ((239-241)Pu) Dissolved in Pacific Ocean Waters Detected by Accelerator Mass Spectrometry: No Effects of the Fukushima Accident Observed.

    Science.gov (United States)

    Hain, Karin; Faestermann, Thomas; Fimiani, Leticia; Golser, Robin; Gómez-Guzmán, José Manuel; Korschinek, Gunther; Kortmann, Florian; Lierse von Gostomski, Christoph; Ludwig, Peter; Steier, Peter; Tazoe, Hirofumi; Yamada, Masatoshi

    2017-02-21

    The concentration of plutonium (Pu) and the isotopic ratios of (240)Pu to (239)Pu and (241)Pu to (239)Pu were determined by accelerator mass spectrometry (AMS) in Pacific Ocean water samples (20 L each) collected in late 2012. The isotopic Pu ratios are important indicators of different contamination sources and were used to identify a possible release of Pu into the ocean by the Fukushima Daiichi Nuclear Power Plant (FDNPP) accident. In particular, (241)Pu is a well-suited indicator for a recent entry of Pu because (241)Pu from fallout of nuclear weapon testings has already significantly decayed. A total of 10 ocean water samples were prepared at the Radiochemie München of the TUM and analyzed at the Vienna Environmental Research Laboratory (VERA). Several samples showed a slightly elevated (240)Pu/(239)Pu ratio of up to 0.22 ± 0.02 compared to global fallout ((240)Pu/(239)Pu = 0.180 ± 0.007), whereas all measured (241)Pu-to-(239)Pu ratios were consistent with nuclear weapon fallout ((241)Pu/(239)Pu < 2.4 × 10(-3)), which means that no impact from the Fukushima accident was detected. From the average (241)Pu-to-(239)Pu ratio of 8-2(+3) ×10(-4) at a sampling station located at a distance of 39.6 km to FDNPP, the 1-σ upper limit for the FDNPP contribution to the (239)Pu inventory in the water column was estimated to be 0.2%. Pu, with the signature of weapon-grade Pu was found in a single sample collected around 770 km off the west coast of the United States.

  18. Assinatura da deposição atmosférica de testes nucleares em sedimentos da costa brasileira (240+239Pu e 137Cs

    Directory of Open Access Journals (Sweden)

    Christian J. Sanders

    2012-01-01

    Full Text Available The aim of this review is to take a look at Cold War era nuclear tests signatures found in Brazilian coastal sediments. Both137Cs and 240+239Pu signatures have been documented in mangrove, coastal mudflats and continental shelf sediments, associated with above ground nuclear tests beginning in the 1950's. The dates associated to the anthropogenic radionuclide signatures 137Cs and 240+239Pu along sediment columns are confirmed by 210Pb geochronology in many of the studies highlighted in this review. The results outlined in this review characterize the extent to which nuclear fallout products reach the Brazilian coast in quantities sufficient for detection, allowing the use of these radioisotopes as geochronometers.

  19. Determination of the {sup 240}Pu/{sup 239}Pu atom ratio in low activity environmental samples by alpha spectrometry and spectral deconvolution

    Energy Technology Data Exchange (ETDEWEB)

    Leon Vintro, L. [University Coll., Dublin (Ireland). Dept. of Experimental Phys.; Mitchell, P.I. [University Coll., Dublin (Ireland). Dept. of Experimental Phys.; Condren, O.M. [University Coll., Dublin (Ireland). Dept. of Experimental Phys.; Moran, M. [Lawrence Livermore National Lab., Livermore, CA (United States); Vives i Batlle, J. [University Coll., Dublin (Ireland). Dept. of Experimental Phys.; Sanchez-Cabeza, J.A. [Dept. de Fisica, Universidad Autonoma de Barcelona, Bellaterra (Spain)

    1996-02-01

    In this paper, a simple technique, based on commercially-available software developed for gamma spectra analysis (MicroSAMPO {sup trademark}), is described by which this complex multiplet can be resolved at the much lower activities typical of many environmental samples. In our approach, it is not necessary to make any alterations to the normal alpha spectrometric set-up (including energy dispersion), other than to improve collimation. The instrumental function is defined for each spectrum by fitting a modified gaussian with exponential tails to the comparatively well-resolved {sup 242}Pu ``doublet`` (used as tracer) and, if present, the {sup 238}Pu ``doublet``. The fitted peaks are used to create an energy calibration file with which, using published energy data, the positions (in channels) of the component peaks of the multiplet are predicted. These positions are not altered subsequently when MicroSAMPO`s interactive multiplet analysis facility is used to quantify the relative spectral intensities of the components. Before calculating the {sup 240}Pu/{sup 239}Pu ratio, it is advisable to correct for coincidence summing of alpha particles and conversion electrons. The technique has been applied to the determination of the {sup 240}Pu/{sup 239}Pu ratio in a set of environmental samples, most of which were supplied by IAEA-MEL under their laboratory intercomparison programme. Subsequently, replicate samples were analysed independently using thermal ionisation mass spectrometry. The agreement between the two sets of data was most satisfactory. Further validation of this deconvolution technique was provided by the good agreement between the measured alpha-emission probabilities for the component peaks in the {sup 239,240}Pu multiplet and published values. (orig.).

  20. Vietnam recommended dietary allowances 2007.

    Science.gov (United States)

    Khan, Nguyen Cong; Hoan, Pham Van

    2008-01-01

    It has been well acknowledged that Vietnam is undergoing a nutrition transition. With a rapid change in the country's reform and economic growth, food supply at the macronutrient level has improved. Changes of the Vietnamese diet include significantly more foods of animal origin, and an increase of fat/oils, and ripe fruits. Consequently, nutritional problems in Vietnam now include not only malnutrition but also overweight/obesity, metabolic syndrome and other chronic diseases related to nutrition and lifestyles. The recognition of these shifts, which is also associated with morbidity and mortality, was a major factor in the need to review and update the Recommended Dietary Allowances (RDA) for the Vietnamese population. This revised RDA established an important science-based tool for evaluation of nutrition adequacy, for teaching, and for scientific communications within Vietnam. It is expected that the 2007 Vietnam RDA and its conversion to food-based dietary guidelines will facilitate education to the public, as well as the policy implementation of programs for prevention of non-communicable chronic diseases and addressing the double burden of both under and over nutrition.

  1. N=151 Pu,Cm and Cf nuclei under rotational stress: Role of higher-order deformations

    Energy Technology Data Exchange (ETDEWEB)

    Hota, S.S., E-mail: sankha.hota@anu.edu.au [Department of Physics, University of Massachusetts Lowell, Lowell, MA 01854 (United States); Chowdhury, P., E-mail: partha_chowdhury@uml.edu [Department of Physics, University of Massachusetts Lowell, Lowell, MA 01854 (United States); Khoo, T.L.; Carpenter, M.P.; Janssens, R.V.F. [Argonne National Laboratory, Argonne, IL 60439 (United States); Qiu, Y. [Department of Physics, University of Massachusetts Lowell, Lowell, MA 01854 (United States); Ahmad, I.; Greene, J.P. [Argonne National Laboratory, Argonne, IL 60439 (United States); Tandel, S.K. [Department of Physics, University of Massachusetts Lowell, Lowell, MA 01854 (United States); Seweryniak, D.; Zhu, S.; Bertone, P.F. [Argonne National Laboratory, Argonne, IL 60439 (United States); Chiara, C.J. [Argonne National Laboratory, Argonne, IL 60439 (United States); Department of Chemistry and Biochemistry, University of Maryland, College Park, MD 20742 (United States); Deo, A.Y.; D' Olympia, N. [Department of Physics, University of Massachusetts Lowell, Lowell, MA 01854 (United States); Gros, S. [Argonne National Laboratory, Argonne, IL 60439 (United States); Guess, C.J.; Harrington, T. [Department of Physics, University of Massachusetts Lowell, Lowell, MA 01854 (United States); Hartley, D.J. [Department of Physics, US Naval Academy, Annapolis, MD 21402 (United States); Henning, G. [Argonne National Laboratory, Argonne, IL 60439 (United States); and others

    2014-12-12

    Fast-rotating N=151 isotones {sup 245}Pu, {sup 247}Cm and {sup 249}Cf have been studied through inelastic excitation and transfer reactions with radioactive targets. While all have a ground-state band built on a νj{sub 15/2}[734]9/2{sup −} Nilsson configuration, new excited bands have also been observed in each isotone. These odd-N excited bands allow a comparison of the alignment behavior for two different configurations, where the νj{sub 15/2} alignment is either blocked or allowed. The effect of higher order deformations is explored through cranking calculations, which help clarify the elusive nature of νj{sub 15/2} alignments.

  2. Melting behavior of (Th,U)O2 and (Th,Pu)O2 mixed oxides

    Science.gov (United States)

    Ghosh, P. S.; Kuganathan, N.; Galvin, C. O. T.; Arya, A.; Dey, G. K.; Dutta, B. K.; Grimes, R. W.

    2016-10-01

    The melting behaviors of pure ThO2, UO2 and PuO2 as well as (Th,U)O2 and (Th,Pu)O2 mixed oxides (MOX) have been studied using molecular dynamics (MD) simulations. The MD calculated melting temperatures (MT) of ThO2, UO2 and PuO2 using two-phase simulations, lie between 3650-3675 K, 3050-3075 K and 2800-2825 K, respectively, which match well with experiments. Variation of enthalpy increments and density with temperature, for solid and liquid phases of ThO2, PuO2 as well as the ThO2 rich part of (Th,U)O2 and (Th,Pu)O2 MOX are also reported. The MD calculated MT of (Th,U)O2 and (Th,Pu)O2 MOX show good agreement with the ideal solidus line in the high thoria section of the phase diagram, and evidence for a minima is identified around 5 atom% of ThO2 in the phase diagram of (Th,Pu)O2 MOX.

  3. Sequential process test for metal pyro-processing using U, Pu, and Am

    Energy Technology Data Exchange (ETDEWEB)

    Masaki Kurata; Noboru Yahagi [Central research Institute of Electric Power Industry, Iwadokita 2-11-1, Komae, Tokyo 201-8511 (Japan); Shinichi Kitawaki; Akira Nakayoshi; Mineo Fukushima [Japan Atomic Energy Agency, Muramatsu 4-33, Tokai-mura, Naka-gun, Ibaraki 319-1194 (Japan)

    2008-07-01

    The Central Research Institute of Electric Power Industry (CRIEPI) and the Japan Atomic Energy Agency (JAEA) are continuing a collaboration study for metal pyro-processing, in which sequential process tests have been performed under practical conditions using {approx}1 kg of molten salt baths. Recent results on two kinds of sequential process test are reported. The former is the electro-chemical reduction test of MOX pellet in order to form U-Pu alloy ingots. The latter is the electrolysis test using a combination of U-Pu alloy anode and solid or liquid cadmium cathode to recover U-product or U-Pu-Am alloy product, respectively. Variation in electrode potentials, current efficiency, molten salt composition, Pu- or Am-impurity in the U-product, U/Pu or Am/Pu separation factor in the U-Pu alloy product, and etc. were measured. These tests reproduced practical operating conditions at a scale of {approx}1/1000 that of the actual process. (author)

  4. Change Spectroscopic, thermal and mechanical studies of PU/PVC blends

    Energy Technology Data Exchange (ETDEWEB)

    Hezma, A.M. [Spectroscopy Department, Physics Division, National Research Center, Giza (Egypt); Elashmawi, I.S. [Spectroscopy Department, Physics Division, National Research Center, Giza (Egypt); Physic Department, Faculty of Science, Taibah University, Al-Ula (Saudi Arabia); Rajeh, A., E-mail: a.rajeh88@yahoo.com [Physic Department, Faculty of Science, Amran University, Sa' dah (Yemen); Physics Department, Faculty of science, Mansoura University, Mansoura (Egypt); Kamal, Mustafa [Physics Department, Faculty of science, Mansoura University, Mansoura (Egypt)

    2016-08-15

    Blends of polyurethane (PU) and polyvinyl chloride (PVC) with different concentrations were prepared by casting method. The effects of PU on PVC blends was examined by Fourier transform-infrared (FTIR), Ultra-violet visible studies (UV/VIS.), X-ray diffraction (XRD), Thermogravimetric (TGA), Differential scanning calorimetry (DSC), and mechanical properties (stress–strain curve). The interaction between PU and PVC was examined by FT-IR through the absorbance of the N–H groups and was correlated to mechanical/thermal properties. Ultra-violet visible said that optical energy gap decrease with increasing concentration of PU. Differential scanning calorimetry results was observed a single glass transition temperature (T{sub g}) for blends this confirming existence miscibility within the blends. The causes for best thermal stability of some blends may be described by measurements of interactions between C=O groups of PU and the α-hydrogen of PVC or a dipole–dipole –C=O..Cl–C– interactions. Significant alterations in FTIR, X-ray and DSC examination shows an interactions between blends had good miscibility. X-ray shows some alterations in the intensity with additional PU. PU change the mechanical behavior of PVC through of the blends. When polyurethane content increase causes polyvinyl chloride tensile strength decreases and elongation at break increase.

  5. Langerhans cells are generated by two distinct PU.1-dependent transcriptional networks.

    Science.gov (United States)

    Chopin, Michaël; Seillet, Cyril; Chevrier, Stéphane; Wu, Li; Wang, Hongsheng; Morse, Herbert C; Belz, Gabrielle T; Nutt, Stephen L

    2013-12-16

    Langerhans cells (LCs) are the unique dendritic cells found in the epidermis. While a great deal of attention has focused on defining the developmental origins of LCs, reports addressing the transcriptional network ruling their differentiation remain sparse. We addressed the function of a group of key DC transcription factors-PU.1, ID2, IRF4, and IRF8-in the establishment of the LC network. We show that although steady-state LC homeostasis depends on PU.1 and ID2, the latter is dispensable for bone marrow-derived LCs. PU.1 controls LC differentiation by regulating the expression of the critical TGF-β responsive transcription factor RUNX3. PU.1 directly binds to the Runx3 regulatory elements in a TGF-β-dependent manner, whereas ectopic expression of RUNX3 rescued LC differentiation in the absence of PU.1 and promoted LC differentiation from PU.1-sufficient progenitors. These findings highlight the dual molecular network underlying LC differentiation, and show the central role of PU.1 in these processes.

  6. Minimal PU.1 reduction induces a preleukemic state and promotes development of acute myeloid leukemia.

    Science.gov (United States)

    Will, Britta; Vogler, Thomas O; Narayanagari, Swathi; Bartholdy, Boris; Todorova, Tihomira I; da Silva Ferreira, Mariana; Chen, Jiahao; Yu, Yiting; Mayer, Jillian; Barreyro, Laura; Carvajal, Luis; Neriah, Daniela Ben; Roth, Michael; van Oers, Johanna; Schaetzlein, Sonja; McMahon, Christine; Edelmann, Winfried; Verma, Amit; Steidl, Ulrich

    2015-10-01

    Modest transcriptional changes caused by genetic or epigenetic mechanisms are frequent in human cancer. Although loss or near-complete loss of the hematopoietic transcription factor PU.1 induces acute myeloid leukemia (AML) in mice, a similar degree of PU.1 impairment is exceedingly rare in human AML; yet, moderate PU.1 inhibition is common in AML patients. We assessed functional consequences of modest reductions in PU.1 expression on leukemia development in mice harboring DNA lesions resembling those acquired during human stem cell aging. Heterozygous deletion of an enhancer of PU.1, which resulted in a 35% reduction of PU.1 expression, was sufficient to induce myeloid-biased preleukemic stem cells and their subsequent transformation to AML in a DNA mismatch repair-deficient background. AML progression was mediated by inhibition of expression of a PU.1-cooperating transcription factor, Irf8. Notably, we found marked molecular similarities between the disease in these mice and human myelodysplastic syndrome and AML. This study demonstrates that minimal reduction of a key lineage-specific transcription factor, which commonly occurs in human disease, is sufficient to initiate cancer development, and it provides mechanistic insight into the formation and progression of preleukemic stem cells in AML.

  7. Change Spectroscopic, thermal and mechanical studies of PU/PVC blends

    Science.gov (United States)

    Hezma, A. M.; Elashmawi, I. S.; Rajeh, A.; Kamal, Mustafa

    2016-08-01

    Blends of polyurethane (PU) and polyvinyl chloride (PVC) with different concentrations were prepared by casting method. The effects of PU on PVC blends was examined by Fourier transform-infrared (FTIR), Ultra-violet visible studies (UV/VIS.), X-ray diffraction (XRD), Thermogravimetric (TGA), Differential scanning calorimetry (DSC), and mechanical properties (stress-strain curve). The interaction between PU and PVC was examined by FT-IR through the absorbance of the N-H groups and was correlated to mechanical/thermal properties. Ultra-violet visible said that optical energy gap decrease with increasing concentration of PU. Differential scanning calorimetry results was observed a single glass transition temperature (Tg) for blends this confirming existence miscibility within the blends. The causes for best thermal stability of some blends may be described by measurements of interactions between C=O groups of PU and the α-hydrogen of PVC or a dipole-dipole -C=O..Cl-C- interactions. Significant alterations in FTIR, X-ray and DSC examination shows an interactions between blends had good miscibility. X-ray shows some alterations in the intensity with additional PU. PU change the mechanical behavior of PVC through of the blends. When polyurethane content increase causes polyvinyl chloride tensile strength decreases and elongation at break increase.

  8. The interception and retention of 238Pu deposition by orange trees.

    Science.gov (United States)

    Pinder, J E; Adriano, D C; Ciravolo, T G; Doswell, A C; Yehling, D M

    1987-06-01

    Radioisotope thermoelectric generators (RTG) transform the heat produced during the alpha decay of 238Pu into electrical energy for use by deep-space probes, such as the Voyager spacecraft, which have returned images and other data from Jupiter, Saturn and Uranus. Future missions involving RTGs may be launched aboard the space shuttle, and there is a remote possibility that an explosion of liquid-hydrogen and liquid-oxygen fuel could rupture the RTGs and disperse 238Pu into the atmosphere over central Florida. Research was performed to determine the potential transport to man of atmospherically dispersed Pu via contaminated orange fruits. The results indicate that the major contamination of oranges would result from the interception and retention of 238Pu deposition by fruits. The resulting surface contamination could enter human food chains through transfer to internal tissues during peeling or in the reconstituted juices and flavorings made from orange skins. The interception of 238Pu deposition by fruits is especially important because the results indicate no measurable loss of Pu from fruit surfaces through time or with washing. Approximately 1% of the 238Pu deposited onto an orange grove would be harvested in the year following deposition.

  9. EnEnvironmental Mobility of Pu(IV) in the Presence of Ethylenediaminetetraacetic Acid: Myth or Reality

    Energy Technology Data Exchange (ETDEWEB)

    Rai, Dhanpat; Moore, Dean A.; Rosso, Kevin M.; Felmy, Andrew R.; Bolton, Harvey

    2008-07-01

    Ethylenediaminetetracetic acid (EDTA), which was co-disposed with Pu at several U. S. Department of Energy sites, has been reported to enhance the solubility and transport of Pu. It is generally assumed that this enhanced transport of Pu in geologic environments is a result of complexation of Pu(IV) with EDTA. However, the fundamental bases for this assumption have never been fully explored. Whether EDTA can mobilize Pu(IV) in geologic environments is dependent on many factors, chief among them are not only the complexation constants of Pu with EDTA and dominant oxidation state and the nature of Pu solids, but also 1) the complexation constants of environmentally important metal ions (e.g. Fe, Al, Ca, Mg) that compete with Pu for EDTA and 2) EDTA interactions with geomedia (e.g., adsorption, biodegradation) that reduce effective EDTA concentrations available for complexation. Extensive studies over a large range of pH values (1 to 14) and EDTA concentrations (0.0001 to 0.01 M) as a function of time were conducted on the solubility of 2-line ferrihydrite (Fe(OH)3(s)), PuO2(am) in the presence of different concentrations of Ca ions, and mixtures of PuO2(am) and Fe(OH)3(s). The solubility data were interpreted using Pitzer’s ion-interaction approach to determine/validate the solubility product of Fe(OH)3(s), the complexation constants of Pu(IV)-EDTA and Fe(III)-EDTA, and to determine the affect of EDTA in solubilizing Pu(IV) from PuO2(am) in the presence of Fe(III) compounds and aqueous Ca concentrations. Predictions based on these extensive fundamental data show that environmental mobility of Pu as a result of Pu(IV)-EDTA complexation as reported/implied in the literature is a myth rather than the reality.

  10. Adipocyte expression of PU.1 transcription factor causes insulin resistance through upregulation of inflammatory cytokine gene expression and ROS production.

    Science.gov (United States)

    Lin, Ligen; Pang, Weijun; Chen, Keyun; Wang, Fei; Gengler, Jon; Sun, Yuxiang; Tong, Qiang

    2012-06-15

    We have reported previously that ETS family transcription factor PU.1 is expressed in mature adipocytes of white adipose tissue. PU.1 expression is increased greatly in mouse models of genetic or diet-induced obesity. Here, we show that PU.1 expression is increased only in visceral but not subcutaneous adipose tissues of obese mice, and the adipocytes are responsible for this increase in PU.1 expression. To further address PU.1's physiological function in mature adipocytes, PU.1 was knocked down in 3T3-L1 cells using retroviral-mediated expression of PU.1-targeting shRNA. Consistent with previous findings that PU.1 regulates its target genes, such as NADPH oxidase subunits and proinflammatory cytokines in myeloid cells, the mRNA levels of proinflammatory cytokines (TNFα, IL-1β, and IL-6) and cytosolic components of NADPH oxidase (p47phox and p40phox) were downregulated significantly in PU.1-silenced adipocytes. NADPH oxidase is a main source for reactive oxygen species (ROS) generation. Indeed, silencing PU.1 suppressed NADPH oxidase activity and attenuated ROS in basal or hydrogen peroxide-treated adipocytes. Silencing PU.1 in adipocytes suppressed JNK1 activation and IRS-1 phosphorylation at Ser(307). Consequently, PU.1 knockdown improved insulin signaling and increased glucose uptake in basal and insulin-stimulated conditions. Furthermore, knocking down PU.1 suppressed basal lipolysis but activated stimulated lipolysis. Collectively, these findings indicate that obesity induces PU.1 expression in adipocytes to upregulate the production of ROS and proinflammatory cytokines, both of which lead to JNK1 activation, insulin resistance, and dysregulation of lipolysis. Therefore, PU.1 might be a mediator for obesity-induced adipose inflammation and insulin resistance.

  11. Application of a canine {sup 238}Pu dosimetry model to human bioassay data

    Energy Technology Data Exchange (ETDEWEB)

    Hickman, A.W. Jr. [Florida Univ., Gainesville, FL (United States)

    1991-08-01

    Associated with the use of 2{sup 238}Pu in thermoelectric power sources for space probes and power supplies for cardiac devices is the potential for human exposure to {sup 238}Pu, primarily by inhalation. In the event of human internal exposure, a means is needed for assessing the level of intake and calculating radiation doses. Several bioassay/dosimetry models have been developed for {sup 239}Pu. However, results from studies with laboratory animals have indicated that the biokinetics, and therefore the descriptive models, of {sup 238}Pu are significantly different from those for {sup 239}Pu. A canine model accounting for these differences has been applied in this work to urinary excretion data from seven humans occupationally exposed to low levels of an insoluble {sup 238}Pu compound. The modified model provides a good description of the urinary excretion kinetics observed in the exposed humans. The modified model was also used to provide estimates of the initial intakes of {sup 238}Pu for the seven individuals; these estimates ranged from 4.5 nCi (170 Bq) to 87 nCi (3200 Bq). Autopsy data on the amount and distribution of {sup 238}Pu retained in the organs may be used in the future to validate or refute both these estimates and the assumptions used to formulate the human model. Modification of the human model to simulate an injection exposure to {sup 239}Pu gave patterns of retention in the organs and urinary excretion comparable to those seen previously in humans; further modification of the model using fecal data (unavailable for the subjects of this study) is indicated.

  12. Application of a canine 238Pu dosimetry model to human bioassay data

    Energy Technology Data Exchange (ETDEWEB)

    Hickman, Jr., A. W. [Florida Univ., Gainesville, FL (United States)

    1991-08-01

    Associated with the use of 2238Pu in thermoelectric power sources for space probes and power supplies for cardiac devices is the potential for human exposure to 238Pu, primarily by inhalation. In the event of human internal exposure, a means is needed for assessing the level of intake and calculating radiation doses. Several bioassay/dosimetry models have been developed for 239Pu. However, results from studies with laboratory animals have indicated that the biokinetics, and therefore the descriptive models, of 238Pu are significantly different from those for 239Pu. A canine model accounting for these differences has been applied in this work to urinary excretion data from seven humans occupationally exposed to low levels of an insoluble 238Pu compound. The modified model provides a good description of the urinary excretion kinetics observed in the exposed humans. The modified model was also used to provide estimates of the initial intakes of 238Pu for the seven individuals; these estimates ranged from 4.5 nCi (170 Bq) to 87 nCi (3200 Bq). Autopsy data on the amount and distribution of 238Pu retained in the organs may be used in the future to validate or refute both these estimates and the assumptions used to formulate the human model. Modification of the human model to simulate an injection exposure to 239Pu gave patterns of retention in the organs and urinary excretion comparable to those seen previously in humans; further modification of the model using fecal data (unavailable for the subjects of this study) is indicated.

  13. 聚氨酯/碳纳米管复合材料的疏水性能研究%Hydrophobic Properties of PU/CNTs composites

    Institute of Scientific and Technical Information of China (English)

    余桂英; 李小兵

    2012-01-01

    The polyurethane/carbon nanotubes (PU/CNTs) composites were produced by solution-blending method. The effects of CNTs content and dispersion method on the hydrophobic property of the composites were analyzed. The results indicated that the random distribution of CNTs bundle provided micron/nano dual rough structure, which had strong hydrophobic nature with a high porosity and surface area. The water contact angle of PU/CNTs composites firstly increased and then decreased with the increase of CNTs content. And when the CNTs content was 5% , the contact angle reached a maximum of 111. 52°. The contact angle increased gradually along with the dispersion time, and appeared a slight drop after the dispersion of 2.0h, thus the best dispersion time was 2. Oh. The order of the dispersion method according to contact angle from high to low was ultrasonic dispersion, magnetic dispersion, mechanical dispersion, therefroe the best dispersion method was ultrasonic dispersion.%采用溶液共混法制备聚氨酯(PU)/碳纳米管(CNTs)复合材料,并探讨碳纳米管含量和分散方法对PU/CNTs复合材料疏水性能的影响.实验结果表明,随机分布的CNTs丛提供了微米/纳米的双重粗糙结构,这种结构具有较大的孔隙率和比表面积,具有较强的疏水性质.PU/CNTs复合材料表面的水接触角随着CNTs含量的增加呈现先增大后减小的趋势,且当ω(CNTs)=5%时水接触角达到最大值111.52°;水接触角随着分散时间的延长逐渐增大,分散超过2.0h后出现了略微的下降,最佳的分散时间是2.0h;在采用不同分散方法制得的PU/CNTs中,水接触角由高到低依次是超声分散、磁力分散、机械分散,最佳分散方法为超声分散.

  14. Pu-Erh tea and GABA attenuates oxidative stress in kainic acid-induced status epilepticus

    OpenAIRE

    2011-01-01

    Abstract Background Pu-Erh tea is one of the most-consumed beverages due to its taste and the anti-anxiety-producing effect of the gamma-aminobutyric acid (GABA) if contains. However the protective effects of Pu-Erh tea and its constituent, GABA to kainic acid (KA)-induced seizure have not been fully investigated. Methods We analyzed the effect of Pu-Erh tea leaf (PETL) and GABA on KA-induced neuronal injury in vivo and in vitro. Results PETL and GABA reduced the maximal seizure classes, pred...

  15. The microscopic magnetisation of the superconductor PuCoGa{sub 5}

    Energy Technology Data Exchange (ETDEWEB)

    Hiess, A. [Institut Laue Langevin, BP 156, 38042 Grenoble (France)]. E-mail: hiess@ill.fr; Stunault, A. [Institut Laue Langevin, BP 156, 38042 Grenoble (France); Colineau, E. [European Commission, JRC-Institute for Transuranium Elements, Postfach 2340, 76125 Karlsruhe (Germany); Rebizant, J. [European Commission, JRC-Institute for Transuranium Elements, Postfach 2340, 76125 Karlsruhe (Germany); Wastin, F. [European Commission, JRC-Institute for Transuranium Elements, Postfach 2340, 76125 Karlsruhe (Germany); Kernavanois, N. [Institut Laue Langevin, BP 156, 38042 Grenoble (France); McIntyre, G.J. [Institut Laue Langevin, BP 156, 38042 Grenoble (France); Fernandez-Diaz, M.T. [Institut Laue Langevin, BP 156, 38042 Grenoble (France); Lelievre-Berna, E. [Institut Laue Langevin, BP 156, 38042 Grenoble (France); Paixao, J.A. [Physics Department, University of Coimbra, Coimbra 3004-516 (Portugal); Lander, G.H. [European Commission, JRC-Institute for Transuranium Elements, Postfach 2340, 76125 Karlsruhe (Germany)

    2007-03-15

    The intermetallic compound PuCoGa{sub 5} is a superconductor with a surprisingly high critical temperature of T{sub sc}=18K in which the superconductivity has been suggested to arise from magnetic fluctuations. We investigated the microscopic magnetic properties by polarised neutron diffraction on a single crystal of {sup 242}PuCoGa{sub 5}. An induced moment is observed on both the Pu and the Co sites. The total magnetisation is significantly smaller than previously reported in agreement with recent magnetisation measurements. This result challenges the currently discussed models for the superconductivity in this weakly magnetic compound.

  16. PU.1 Suppresses Th2 Cytokine Expression via Silencing of GATA3 Transcription in Dendritic Cells.

    Science.gov (United States)

    Yashiro, Takuya; Kubo, Masato; Ogawa, Hideoki; Okumura, Ko; Nishiyama, Chiharu

    2015-01-01

    The transcription factor PU.1 is predominantly expressed in dendritic cells (DCs) and is essential for DC differentiation. Although there are several reports that PU.1 positively regulates the expression of DC-specific genes, whether PU.1 also has a suppressive effect on DCs is largely unknown. Here we demonstrate that PU.1 suppresses the expression of Th2 cytokines including IL-13 and IL-5 in bone marrow-derived DCs (BMDCs), through repression of the expression of GATA3, which is a master regulator of Th2 differentiations. When PU.1 siRNA was introduced into BMDCs, LPS-induced expression of IL-13 and IL-5 was increased along with upregulation of the constitutive expression of GATA2 and GATA3. The additional introduction of GATA3 siRNA but not of GATA2 siRNA abrogated PU.1 siRNA-mediated upregulation of IL-13 and IL-5. A chromatin immunoprecipitation assay showed that PU.1 bound to Gata3 proximal promoter region, which is more dominant than the distal promoter in driving GATA3 transcription in DCs. The degree of histone acetylation at the Gata3 promoter was decreased in PU.1 siRNA-introduced DCs, suggesting the involvement of PU.1 in chromatin modification of the Gata3 promoter. Treatment with a histone deacetylase (HDAC) inhibitor, trichostatin A, increased the degree of histone H3 acetylation at the Gata3 promoter and induced the subsequent expression of GATA3. Experiments using HDAC inhibitors and siRNAs showed that HDAC3 suppressed GATA3 expression. The recruitment of HDAC3 to the Gata3 promoter was decreased by PU.1 knockdown. LPS-induced IL-13 expression was dramatically reduced in BMDCs generated from mice lacking the conserved GATA3 response element, termed CGRE, which is an essential site for the binding of GATA3 on the Il-13 promoter. The degree of H3K4me3 at CGRE was significantly increased in PU.1 siRNA-transfected stimulated DCs. Our results indicate that PU.1 plays pivotal roles in DC development and function, serving not only as a transcriptional

  17. I-Pu-Xe dating and the relative ages of the earth and moon

    Science.gov (United States)

    Swindle, T. D.; Caffee, M. W.; Hohenberg, C. M.; Taylor, S. R.

    1986-01-01

    The ages of the earth and moon as determined by various chronometric systems are discussed with primary emphasis placed on the development of an I-Pu-Xe chronometer. Data on excess fission xenon are reviewed with attention given to the strengths and weaknesses of the assumptions required for lunar I-Pu-Xe chronometry. Using I-Pu-Xe dating, it is estimated that the retention of excess fission xenon in lunar samples began no more than 63 + or - 42 m.y. after the time of primitive meteorite formation.

  18. Analytical method for the determination of Np and Pu in sea water by AMS with respect to the Fukushima accident

    Energy Technology Data Exchange (ETDEWEB)

    Hain, K., E-mail: karin.hain@mytum.de [Physics Department, Technische Universität München, James-Franck-Str.1, 85748 Garching (Germany); Faestermann, T.; Famulok, N.; Fimiani, L.; Gómez-Guzmán, J.M.; Korschinek, G. [Physics Department, Technische Universität München, James-Franck-Str.1, 85748 Garching (Germany); Kortmann, F.; Lierse von Gostomski, Ch. [Radiochemie München, Technische Universität München, Walther-Meißner-Str.3, 85748 Garching (Germany); Ludwig, P. [Physics Department, Technische Universität München, James-Franck-Str.1, 85748 Garching (Germany); Shinonaga, T. [Helmholtz Zentrum München, German Research Center for Environmental Health, Institute of Radiation Protection, Ingolstädter Landstrasse 1, 855764 Neuherberg (Germany)

    2015-10-15

    A chemical separation procedure for plutonium (Pu) and neptunium (Np) was developed using extraction chromatography, mass spectrometry and radiometric analysis to determine their concentrations and isotopic ratios in sea water. {sup 241}Am, which causes isobaric background to {sup 241}Pu in mass spectrometric measurements, was successfully separated from the Pu fraction by this method. Water samples which were spiked with {sup 242}Pu and {sup 237}Np or {sup 239}Np, respectively, were used for chemical yield determination. The chemical yields of Pu and Np, which were determined by alpha and gamma spectrometry at the Radiochemie München (RCM), of more than 85% were obtained. The developed method was applied to analyze the concentration of Pu and Np in the certified reference material, IAEA-443, by Accelerator Mass Spectrometry (AMS) at the Maier–Leibnitz-Laboratory (MLL) to check the applicability of the method to sea water samples. The concentrations of {sup 240}Pu, {sup 241}Pu and {sup 237}Np obtained in this study are in agreement with the certified and literature values within the uncertainties. Due to strong isotopic interference of {sup 239}Pu with {sup 238}U, it was not possible to analyze the concentration of {sup 239}Pu. Some modifications of the chemical separation method to suppress the uranium (U) fraction are under consideration. This method can be used for the analysis of Pu and Np in Pacific Ocean water samples collected after the Fukushima accident.

  19. Simultaneous determination of catechins, caffeine and gallic acids in green, Oolong, black and pu-erh teas using HPLC with a photodiode array detector.

    Science.gov (United States)

    Zuo, Yuegang; Chen, Hao; Deng, Yiwei

    2002-05-16

    A simple and fast HPLC method using a photodiode array detector was developed for simultaneous determination of four major catechins, gallic acid and caffeine. After multiple extractions with aqueous methanol and acidic methanol solutions, tea extract was separated within 20 min using a methanol-acetate-water buffer gradient elution system on a C(18) column. The sample extraction data demonstrated that the single extraction used in the previous studies with aqueous acetonitrile or methanol is not sufficient; the multiple extraction procedure is essential for the quantitative analysis of catechins, phenolic acids and caffeine in teas. Several green, Oolong, black and pu-erh teas were successfully analyzed by this method. The analytical results obtained indicated that green teas contain higher content of catechins [(-)-epigallocatechin gallate, (-)-epigallocatechin, (-)-epicatechin gallate, and (-)-epicatechin] than both Oolong, pu-erh and black teas because fermentation process during the tea manufacturing reduced the levels of catechins significantly. The fermentation process also remarkably elevated the levels of gallic acid in full-fermented pu-erh and black teas. Another interesting finding is the low level of caffeine in Oolong teas, especially in Fujian Oolong tea.

  20. ZPR-6 assembly 7 high {sup 240} PU core : a cylindrical assemby with mixed (PU, U)-oxide fuel and a central high {sup 240} PU zone.

    Energy Technology Data Exchange (ETDEWEB)

    Lell, R. M.; Schaefer, R. W.; McKnight, R. D.; Tsiboulia, A.; Rozhikhin, Y.; Nuclear Engineering Division; Inst. of Physics and Power Engineering

    2007-10-01

    Over a period of 30 years more than a hundred Zero Power Reactor (ZPR) critical assemblies were constructed at Argonne National Laboratory. The ZPR facilities, ZPR-3, ZPR-6, ZPR-9 and ZPPR, were all fast critical assembly facilities. The ZPR critical assemblies were constructed to support fast reactor development, but data from some of these assemblies are also well suited to form the basis for criticality safety benchmarks. Of the three classes of ZPR assemblies, engineering mockups, engineering benchmarks and physics benchmarks, the last group tends to be most useful for criticality safety. Because physics benchmarks were designed to test fast reactor physics data and methods, they were as simple as possible in geometry and composition. The principal fissile species was {sup 235}U or {sup 239}Pu. Fuel enrichments ranged from 9% to 95%. Often there were only one or two main core diluent materials, such as aluminum, graphite, iron, sodium or stainless steel. The cores were reflected (and insulated from room return effects) by one or two layers of materials such as depleted uranium, lead or stainless steel. Despite their more complex nature, a small number of assemblies from the other two classes would make useful criticality safety benchmarks because they have features related to criticality safety issues, such as reflection by soil-like material. The term 'benchmark' in a ZPR program connotes a particularly simple loading aimed at gaining basic reactor physics insight, as opposed to studying a reactor design. In fact, the ZPR-6/7 Benchmark Assembly (Reference 1) had a very simple core unit cell assembled from plates of depleted uranium, sodium, iron oxide, U3O8, and plutonium. The ZPR-6/7 core cell-average composition is typical of the interior region of liquid-metal fast breeder reactors (LMFBRs) of the era. It was one part of the Demonstration Reactor Benchmark Program,a which provided integral experiments characterizing the important features of

  1. /sup 238/Pu fuel form activities, October 1, 1985-March 31, 1986

    Energy Technology Data Exchange (ETDEWEB)

    Ortaldo, J. F.

    1986-07-01

    This report summarizes production of /sup 238/PuO/sub 2/ fuel forms for use in radioisotopic thermoelectric generators (RTG's) in the Plutonium Fuel Form (Puff) Facility at the Savannah River Plant.

  2. Surprising Coordination Geometry Differences in Ce(IV)- and Pu(IV)-Maltol Complexes

    Energy Technology Data Exchange (ETDEWEB)

    Lawrence Berkeley National Laboratory; Raymond, Kenneth; Szigethy, Geza; Xu, Jide; Gorden, Anne E.V.; Teat, Simon J.; Shuh, David K.; Raymond, Kenneth N.

    2008-02-12

    As part of a study to characterize the detailed coordination behavior of Pu(IV), single crystal X-ray diffraction structures have been determined for Pu(IV) and Ce(IV) complexes with the naturally-occurring ligand maltol (3-hydroxy-2-methyl-pyran-4-one) and its derivative bromomaltol (5-bromo-3-hydroxy-2-methyl-pyran-4-one). Although Ce(IV) is generally accepted as a structural analog for Pu(IV), and the maltol complexes of these two metals are isostructural, the corresponding bromomaltol complexes are strikingly different with respect to ligand orientation about the metal ion: All complexes exhibit trigonal dodecahedral coordination geometry but the Ce(IV)-bromomaltol complex displays an uncommon ligand arrangement not mirrored in the Pu(IV) complex, although the two metal species are generally accepted to be structural analogs.

  3. Characterization of a {sup 239}PuBe isotopic neutron source

    Energy Technology Data Exchange (ETDEWEB)

    Vega C, H. R.; Hernandez D, V. M. [Universidad Autonoma de Zacatecas, Unidad Academica de Estudios Nucleares, Cipres No. 10, Fracc. La Penuela, 98068 Zacatecas (Mexico); Rivera M, T. [IPN, Centro de Investigacion en Ciencia Aplicada y Tecnologia Avanzada, Calz. Legaria No. 694, Col. Irrigacion, 11500 Mexico D. F. (Mexico); Sanchez, A., E-mail: fermineutron@yahoo.com [IPN, Escuela Superior de Fisica y Matematicas, 07738 Mexico D. F. (Mexico)

    2012-10-15

    A Bonner sphere spectrometer was used to determine the features of a {sup 239}PuBe neutron source used to operate the ESFM-Ipn Subcritical Reactor. The spectrometer is a {sup 6}Lil(Eu) scintillator and 2, 3, 5, 8, 10 and 12 inches-diameter polyethylene spheres, that was located 100 cm from the neutron source. The count rates obtained with the spectrometer were unfolded using the NSDUAZ code and neutron spectrum, total fluence, and ambient dose equivalent were determined. A Monte Carlo calculation, using the MCNP5 code, was carried out to estimate the spectrum and integral features being less that values obtained experimentally due to the presence of {sup 241}Pu in the Pu used to fabricate the source. Using the experimental information the actual neutron yield and the mass fraction of {sup 241}Pu was estimated. (Author)

  4. Electronic structure of PuMGa5 (M = Co, Rh heavy Fermion compounds

    Directory of Open Access Journals (Sweden)

    A Tavana

    2009-08-01

    Full Text Available  Electronic properties of heavy Fermion superconductors PuCoGa5 and PuRhGa5 consisting of density of states, band structure and the Fermi surface have been calculated based on density functional theory in the local spin density approximation plus on site Coulomb correlation (LSDA+U. Calculated density of states is in overall consistency with a photo emission experiment. The bands with f character in the PuCoGa5 mostly form below the Fermi level while in PuRhGa5 some of these bands shift to above the Fermi energy. Comparison with other calculations implies that application of correlation correction, more separates the j=7/2 and j=5/2 band from each other. Fermi surfaces have been also extracted and discussed .

  5. Feasibility of Burning Civilian Grade Pu in the Modular HTR with Th Fuel Cycle

    Institute of Scientific and Technical Information of China (English)

    许云林; 经荥清

    2001-01-01

    The Modular High Temperature Gas-Cooled Reactor (HTR) can be usedto burn plutonium fuel to reduce Pu stockpiles because of its inherent safety characteristics and ability to burn a variety of fuel mixtures. The equilibrium core is calculated and analyzed for Pu enriched fuel. Fuel spheres with 7 g heavy metal including the civilian grade Pu and thorium are loaded into the reactor. An enrichment of 11% is chosen to provide the desired equilibrium core reactivity. The fuel and moderator temperature coefficients are both negative. The maximum fuel element temperature during normal operation and during a loss of coolant accident is less than 1500 ℃. 92% of 239Pu will be burnt during nomal operation. Therefore, a thorium fuel cycle in the modular HTR is an effective method for burning civilian grade plutonium.

  6. First-principles elastic constants and phonons of delta-Pu

    DEFF Research Database (Denmark)

    Söderlind, P.; Landa, A.; Sadigh, B.

    2004-01-01

    Elastic constants and zone-boundary phonons of delta-plutonium have been calculated within the density-functional theory. The paramagnetic state of delta-Pu is modeled by disordered magnetism utilizing either the disordered local moment or the special quasirandom structure techniques. The anomalo......Elastic constants and zone-boundary phonons of delta-plutonium have been calculated within the density-functional theory. The paramagnetic state of delta-Pu is modeled by disordered magnetism utilizing either the disordered local moment or the special quasirandom structure techniques....... The anomalously soft C-' as well as a large anisotropy ratio (C-44/C-') of delta-Pu is reproduced by this theoretical model. Also the recently measured phonons for delta-Pu compare relatively well with their theoretical counterpart at the zone boundaries....

  7. Study of Pretreatment Method for Measurement of Small Quantity of U, Np, Pu in 1AW

    Institute of Scientific and Technical Information of China (English)

    DENG; Wei-qin; TAN; Shu-ping; WU; Ji-zong; TAO; Miao-miao

    2012-01-01

    <正>The analysis of U, Np, Pu in 1AW plays an important role on monitoring of plutonium and uranium recovery and neptunium distribution in co-decontamination cycle. Due to the high radioactivity and the

  8. Pu`ukohola Heiau National Historic Site Vegetation Mapping Project - Spatial Vegetation Data

    Data.gov (United States)

    National Park Service, Department of the Interior — This metadata is for the vegetation and land-use geo-spatial database for Pu'ukohola Heiau National Historic Site (PUHE) , Island of Hawai'i and surrounding areas....

  9. Spatial distribution of {sup 241}Am, {sup 137}Cs, {sup 238}Pu, {sup 239,240}Pu and {sup 241}Pu over 17 year periods in the Ravenglass saltmarsh, Cumbria, UK

    Energy Technology Data Exchange (ETDEWEB)

    Oh, J.-S. [GAU-Radioanalytical, School of Ocean and Earth Science, National Oceanography Centre, Southampton SO14 3ZH (United Kingdom)], E-mail: jsoh@noc.soton.ac.uk; Warwick, P.E. [GAU-Radioanalytical, School of Ocean and Earth Science, National Oceanography Centre, Southampton SO14 3ZH (United Kingdom)], E-mail: pew@noc.soton.ac.uk; Croudace, I.W. [GAU-Radioanalytical, School of Ocean and Earth Science, National Oceanography Centre, Southampton SO14 3ZH (United Kingdom)], E-mail: iwc@noc.soton.ac.uk

    2009-07-15

    Ninety five surface scrape samples were collected at the Ravenglass saltmarsh and analysed for radionuclides by alpha spectrometry ({sup 238}Pu and {sup 239,240}Pu), gamma spectrometry ({sup 241}Am and {sup 137}Cs) and liquid scintillation counting ({sup 241}Pu). Both {sup 241}Am and {sup 137}Cs activities are compared with those reported by Horrill [1983. Concentrations and spatial distribution of radioactivity in an ungrazed saltmarsh. In: Coughtrey, P.J. (Ed.), Ecological Aspects of Radionuclide Release. British Ecological Society Special Publication No. 3. Blackwell, Oxford, pp. 119-215.] Significant decreases in activities for both radionuclides were observed which is caused by the declining levels of discharges from the Sellafield nuclear reprocessing plant since the 1980s. It has been concluded that the spatial distribution of these radionuclides are controlled by the tidal currents and the clay contents in the sediments. There is evidence of surface erosion of the saltmarsh and redistribution of radionuclides in the saltmarsh using isotopic ratios of measured Pu.

  10. Piezoelectric PU/PVDF electrospun scaffolds for wound healing applications.

    Science.gov (United States)

    Guo, Hong-Feng; Li, Zhen-Sheng; Dong, Shi-Wu; Chen, Wei-Jun; Deng, Ling; Wang, Yu-Fei; Ying, Da-Jun

    2012-08-01

    Previous studies have shown that piezoelectric materials may be used to prepare bioactive electrically charged surfaces. In the current study, polyurethane/polyvinylidene fluoride (PU/PVDF) scaffolds were prepared by electrospinning. The mechanical property and piezoelectric property of the scaffolds were evaluated. The crystalline phase of PVDF in the scaffolds was characterised by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR) and differential scanning calorimetry (DSC). In vitro cell culture was performed to investigate cytocompatibility of the scaffolds. Wound-healing assay, cell-adhesion assay, quantitative RT-PCR and Western blot analyses were performed to investigate piezoelectric effect of the scaffolds on fibroblast activities. Further, the scaffolds were subcutaneously implanted in Sprague-Dawley (SD) rats to investigate their biocompatibility and the piezoelectric effect on fibrosis in vivo. The results indicated that the electrospinning process had changed PVDF crystalline phase from the nonpiezoelectric α phase to the piezoelectric β phase. The fibroblasts cultured on the scaffolds showed normal morphology and proliferation. The fibroblasts cultured on the piezoelectric-excited scaffolds showed enhanced migration, adhesion and secretion. The scaffolds that were subcutaneously implanted in SD rats showed higher fibrosis level due to the piezoelectrical stimulation, which was caused by random animal movements followed by mechanical deformation of the scaffolds. The scaffolds are potential candidates for wound healing applications.

  11. Levels of 232U fed in 236Pu α decay

    Science.gov (United States)

    Ardisson, G.; Hussonnois, M.; Ledu, J. F.; Trubert, D.; Lederer, C. M.

    1994-06-01

    The γ spectrum following the α decay of 236Pu has been reinvestigated with a high-resolution HPGe detector. Accurate energies and intensities are reported for 26 γ transitions, of which 20 were observed for the first time. A decay scheme is constructed using the Ritz combination principle, γγ coincidence data, and previously known data from nuclear reactions and from232Pa β- decay. We observe feeding of the ground-state rotational band up to spin 8, the β vibrational band to spin 4, the K=0 octupole vibrational band to spin 5, and the bandhead of the γ vibrational band. New states of 232U at 927.3 and 967.7 keV, populated with low α-decay hindrance factors, are assigned as members of a second-excited Kπ=0+ band. The ratio of E1/E2 transitions in the decay of these states suggests that the E1 transitions to members of the K=0 octupole band may be rather fast (~=10-3 Weisskopf units). Systematics of hindrance factors for α decay to vibrational states are presented.

  12. Role of PU.1 in MHC Class II Expression via CIITA Transcription in Plasmacytoid Dendritic Cells.

    Science.gov (United States)

    Miura, Ryosuke; Kasakura, Kazumi; Nakano, Nobuhiro; Hara, Mutsuko; Maeda, Keiko; Okumura, Ko; Ogawa, Hideoki; Yashiro, Takuya; Nishiyama, Chiharu

    2016-01-01

    The cofactor CIITA is a master regulator of MHC class II expression and several transcription factors regulating the cell type-specific expression of CIITA have been identified. Although the MHC class II expression in plasmacytoid dendritic cells (pDCs) is also mediated by CIITA, the transcription factors involved in the CIITA expression in pDCs are largely unknown. In the present study, we analyzed the role of a hematopoietic lineage-specific transcription factor, PU.1, in CIITA transcription in pDCs. The introduction of PU.1 siRNA into mouse pDCs and a human pDC cell line, CAL-1, reduced the mRNA levels of MHC class II and CIITA. When the binding of PU.1 to the 3rd promoter of CIITA (pIII) in CAL-1 and mouse pDCs was analyzed by a chromatin immunoprecipitation assay, a significant amount of PU.1 binding to the pIII was detected, which was definitely decreased in PU.1 siRNA-transfected cells. Reporter assays showed that PU.1 knockdown reduced the pIII promoter activity and that three Ets-motifs in the human pIII promoter were candidates of cis-enhancing elements. By electrophoretic mobility shift assays, it was confirmed that two Ets-motifs, GGAA (-181/-178) and AGAA (-114/-111), among three candidates, were directly bound with PU.1. When mouse pDCs and CAL-1 cells were stimulated by GM-CSF, mRNA levels of PU.1, pIII-driven CIITA, total CIITA, MHC class II, and the amount of PU.1 binding to pIII were significantly increased. The GM-CSF-mediated up-regulation of these mRNAs was canceled in PU.1 siRNA-introduced cells. Taking these results together, we conclude that PU.1 transactivates the pIII through direct binding to Ets-motifs in the promoter in pDCs.

  13. The 'granite encapsulation' route to the safe disposal of Pu and other actinides

    Energy Technology Data Exchange (ETDEWEB)

    Gibb, F.G.F. [Immobilisation Science Laboratory, Department of Engineering Materials, University of Sheffield, Sheffield S1 3JD (United Kingdom)], E-mail: f.gibb@sheffield.ac.uk; Taylor, K.J. [Department of Geography, University of Sheffield, Sheffield S10 2TN (United Kingdom); Burakov, B.E. [Laboratory of Applied Mineralogy and Radiogeochemistry, V.G. Khlopin Radium Institute, St. Petersburg 194021 (Russian Federation)

    2008-03-15

    Waste actinides, including plutonium, present a long-term management problem and a serious security issue. Immobilisation in mineral or ceramic waste forms for interim storage is a widely proposed first step. The safest, most secure geological disposal for Pu is in very deep boreholes and we propose that the key step to combination of these immobilisation and disposal concepts is encapsulation of the waste form in cylinders of recrystallized granite. We discuss the underpinning science, focusing on experimental work, and consider implementation. Finally, we present and discuss analyses of zircon, UO{sub 2} and Ce-doped cubic zirconia from high pressure and temperature experiments in granitic melts that demonstrate the viability of this solution and that actinides can be isolated from the environment for millions, maybe hundreds of millions, of years.

  14. Feasibility study of 235U and 239Pu characterization in radioactive waste drums using neutron-induced fission delayed gamma rays

    Science.gov (United States)

    Nicol, T.; Pérot, B.; Carasco, C.; Brackx, E.; Mariani, A.; Passard, C.; Mauerhofer, E.; Collot, J.

    2016-10-01

    This paper reports a feasibility study of 235U and 239Pu characterization in 225 L bituminized waste drums or 200 L concrete waste drums, by detecting delayed fission gamma rays between the pulses of a deuterium-tritium neutron generator. The delayed gamma yields were first measured with bare samples of 235U and 239Pu in REGAIN, a facility dedicated to the assay of 118 L waste drums by Prompt Gamma Neutron Activation Analysis (PGNAA) at CEA Cadarache, France. Detectability in the waste drums is then assessed using the MCNPX model of MEDINA (Multi Element Detection based on Instrumental Neutron Activation), another PGNAA cell dedicated to 200 L drums at FZJ, Germany. For the bituminized waste drum, performances are severely hampered by the high gamma background due to 137Cs, which requires the use of collimator and shield to avoid electronics saturation, these elements being very penalizing for the detection of the weak delayed gamma signal. However, for lower activity concrete drums, detection limits range from 10 to 290 g of 235U or 239Pu, depending on the delayed gamma rays of interest. These detection limits have been determined by using MCNPX to calculate the delayed gamma useful signal, and by measuring the experimental gamma background in MEDINA with a 200 L concrete drum mock-up. The performances could be significantly improved by using a higher interrogating neutron emission and an optimized experimental setup, which would allow characterizing nuclear materials in a wide range of low and medium activity waste packages.

  15. Chemical separation and ICP-AES determination of 22 metallic elements in U and Pu matrices using cyanex-923 extractant and studies on stripping of U and Pu.

    Science.gov (United States)

    Argekar, A A; Kulkarni, M J; Mathur, J N; Page, A G

    2002-03-11

    Comprehensive studies have been carried out on the extraction behavior of uranium and plutonium matrices using cyanex-923 extractant. The near total extraction of U/Pu and quantitative separation of 22 metallic elements at trace levels has been established using inductively coupled plasma-atomic emission spectrometry (ICP-AES). The studies carried out on back extraction of U/Pu from organic phase have established the near total recovery of these matrices into the aqueous phase using 1 M Na(2)CO(3) and saturated oxalic acid, respectively.

  16. High-/sup 240/Pu sector experiments in ZPPR assembly 4

    Energy Technology Data Exchange (ETDEWEB)

    McFarlane, H F; Beck, C L

    1976-12-01

    The complete high-/sup 240/Pu fuel experiment in ZPPR assembly 4 is reviewed. Results of criticality, enrichment, small-sample perturbation, sodium void, /sup 238/U Doppler, control rod substitution and reaction rate measurements are presented. Comparison of these measured values with calculated results are included where possible. The relationship between the ZPPR high-/sup 240/Pu fuel experiments and the results obtained in previous critical experience is considered.

  17. Distribution coefficients for the sorption of Th, U, Np, Pu, and Am on Opalinus Clay

    Energy Technology Data Exchange (ETDEWEB)

    Amayri, Samer; Froehlich, Daniel R.; Kaplan, Ugras; Trautmann, Norbert; Reich, Tobias [Mainz Univ. (Germany). Inst. of Nuclear Chemistry

    2016-04-01

    The distribution coefficients (K{sub d}) are determined for the sorption of Th(IV), U(VI), Np(V), Pu(III/IV/VI), and Am(III) in the system natural Opalinus Clay (OPA) from Mont Terri, Switzerland, and synthetic OPA pore water at pH 7.6 as a function of solid-to-liquid ratio and element concentration. A linear sorption behavior under the chosen experimental conditions was obtained. The K{sub d} values strongly depend on the oxidation state of the actinide. The K{sub d} values for the tri- and tetravalent actinides are in the range of 29-159 m{sup 3}/kg. U and Np in the oxidation states six and five, respectively, are weakly sorbed on OPA with K{sub d} values of 0.04-0.05 m{sup 3}/kg. The K{sub d} values for the redox-stable Am(III) and Th(IV) are in the same range as for Pu(III) and Pu(IV) which are redox sensitive. The K{sub d} value of Pu(VI) (13 ± 3 m{sup 3}/kg) is about one order of magnitude lower than the K{sub d} values of Pu(III) and Pu(IV), but still more than two orders of magnitude higher compared to the values obtained for U(VI) and Np(V). This discrepancy is attributed to the partial reduction of Pu(VI) to Pu(IV) during sorption.

  18. Mass transport properties of Pu/DT mixtures from orbital free molecular dynamics simulations

    Energy Technology Data Exchange (ETDEWEB)

    Kress, Joel David [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Ticknor, Christopher [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Collins, Lee A. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2015-09-16

    Mass transport properties (shear viscosity and diffusion coefficients) for Pu/DT mixtures were calculated with Orbital Free Molecular Dynamics (OFMD). The results were fitted to simple functions of mass density (for ρ=10.4 to 62.4 g/cm3) and temperature (for T=100 up to 3,000 eV) for Pu/DT mixtures consisting of 100/0, 25/75, 50/50, and 75/25 by number.

  19. Methodological Study on AMS Measurement of Ultra-trace Pu Isotope Ratios at CIAE

    Institute of Scientific and Technical Information of China (English)

    DONG; Ke-jun; ZHAO; Qing-zhang; WANG; Chen; HE; Ming; JIANG; Shan; ZHANG; Hui; PANG; Yi-jun; SHEN; Hong-tao; WANG; Xiao-ming; XU; Yong-ning; WU; Shao-yong; YANG; Xu-ran; WANG; Xiang-gao

    2015-01-01

    The determination of ultra-trace plutonium is very important in different fields.A new measurement method of plutonium isotopic ratios with accelerator mass spectrometry(AMS)was developed at China Institute of Atomic Energy(CIAE).Two laboratory reference standards of 239Pu/240 Pu(ST1)and 239Pu/242 Pu(ST2)are17.241and 10.059,a flow blank,a commercial blank and three real samples were respectively

  20. Transcriptional Factor PU.1 Regulates Decidual C1q Expression in Early Pregnancy in Human.

    Science.gov (United States)

    Madhukaran, Shanmuga Priyaa; Kishore, Uday; Jamil, Kaiser; Teo, Boon Heng Dennis; Choolani, Mahesh; Lu, Jinhua

    2015-01-01

    C1q is the first recognition subcomponent of the complement classical pathway, which in addition to being synthesized in the liver, is also expressed by macrophages and dendritic cells (DCs). Trophoblast invasion during early placentation results in accumulation of debris that triggers the complement system. Hence, both early and late components of the classical pathway are widely distributed in the placenta and decidua. In addition, C1q has recently been shown to significantly contribute to feto-maternal tolerance, trophoblast migration, and spiral artery remodeling, although the exact mechanism remains unknown. Pregnancy in mice, genetically deficient in C1q, mirrors symptoms similar to that of human preeclampsia. Thus, regulated complement activation has been proposed as an essential requirement for normal successful pregnancy. Little is known about the molecular pathways that regulate C1q expression in pregnancy. PU.1, an Ets-family transcription factor, is required for the development of hematopoietic myeloid lineage immune cells, and its expression is tissue-specific. Recently, PU.1 has been shown to regulate C1q gene expression in DCs and macrophages. Here, we have examined if PU.1 transcription factor regulates decidual C1q expression. We used immune-histochemical analysis, PCR, and immunostaining to localize and study the gene expression of PU.1 transcription factor in early human decidua. PU.1 was highly expressed at gene and protein level in early human decidual cells including trophoblast and stromal cells. Surprisingly, nuclear as well as cytoplasmic PU.1 expression was observed. Decidual cells with predominantly nuclear PU.1 expression had higher C1q expression. It is likely that nuclear and cytoplasmic PU.1 localization has a role to play in early pregnancy via regulating C1q expression in the decidua during implantation.

  1. Actinide burner fuel: Potential compositions based on the thermodynamic evaluation of MF-PuF 3 (M = Li, Na, K, Rb, Cs) and LaF 3-PuF 3 systems

    Science.gov (United States)

    Beneš, O.; Konings, R. J. M.

    2008-07-01

    In previous studies a thermodynamic description of the LiF-NaF-KF-RbF-CsF-LaF 3 system was presented. In order to add PuF 3 to this system the assessments of LiF-PuF 3, NaF-PuF 3, KF-PuF 3, RbF-PuF 3, CsF-PuF 3 and LaF 3-PuF 3 binary phase diagrams have been made. In case of the LiF-PuF 3 and NaF-PuF 3 the assessments have been based on known experimental data. The other binary systems have not been measured yet and the thermodynamic description has been made using the excess parameters from the previously assessed binaries containing LaF 3, which is considered as a proxy compound for PuF 3. The main aim of this study is to analyze potential compositions for a molten salt fast burner fuel.

  2. Structural characteristics and properties of PU-modified TDE-85/MeTHPA epoxy resin

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Diglycidy1-4,5-epoxycyclohexane-1,2-dicarboxylate (TDE-85)/methyl tetrahydro-phthalic anhydride (MeTHPA) epoxy resin was modified by polyurethane(PU), and its structural characteristics and properties were studied by infrared spectrum analysis(IR), scanning electronic microscopy (SEM), mechanics testing and thermogravimetric analysis (TG). The results indicate that epoxy polymeric network Ⅰ and polyurethane polymeric network Ⅱ are formed in the PU-modified TDE-85/MeTHPA epoxy resin.Meanwhile the PU-modified TDE-85/MeTHPA resins have heterogeneous structure. The miscibility between epoxy (EP) and polyurethane (PU) as well as the phase size are dominantly determined by the mass fraction of polyurethane prepolymer (PUP) in the EP/PU blends. With the increase of PUP mass fraction, the tensile strength, impact strength and thermal stability of the PU-modified TDE-85/MeTHPA epoxy resin all firstly exhibit increasing tendency, and decrease after successively reaching their maxima. When the number-average molecular mass of PPG is 1 000 and the mass fraction of PUP is 15%, the tensile strength, impact strength and thermal stability of materials obtained, compared with TDE-85/MeTHPA epoxy resin, are improved obviously.

  3. Many-body Expanded Analytical Potential Energy Function for Ground State PuOH Molecule

    Institute of Scientific and Technical Information of China (English)

    LI Yue-Xun; GAO Tao; ZHU Zheng-He

    2006-01-01

    Using the density functional method B3LYP with relativistic effective core potential (RECP) for Pu atom, the low-lying excited states (4∑+, 6∑+, 8∑+) for three structures of PuOH molecule were optimized. The results show that the ground state is X6∑+of the linear Pu-O-H (C∞v), its corresponding equilibrium geometry and dissociation energy are RPu-O=0.20595 nm, RO-H=0.09581 nm and -8.68 eV, respectively. At the same time, two other metastable structures [PuOH (Cs) and H-Pu-O (C∞v)] were found. The analytical potential energy function has also been derived for whole range using the many-body expansion method. This potential energy function represents the considerable topographical features of PuOH molecule in detail, which is adequately accurate in the whole potential surface and can be used for the molecular reaction dynamics research.

  4. Narrativas sobre a experiência de ser puérpera de alto risco

    Directory of Open Access Journals (Sweden)

    Ariane Thaise Frello Roque

    2015-06-01

    Full Text Available Objetivo: Quando o puerpério ocorre concomitantemente à hospitalização do recém-nascido, leva a puérpera a tornar-se acompanhante na Unidade Neonatal, o que pode influenciar seu poder vital conceituando-se o Puerpério de Alto Risco. O objetivo deste estudo foi conhecer a experiência de ser puérpera de alto risco. Métodos: Narrativo com abordagem qualitativa, sustentado em Florence Nightingale. Realizado em uma instituição pública do sul do Brasil, de janeiro a março de 2010, foram sujeitos da pesquisa sete puérperas de alto risco acima de 18 anos, sendo neste recorte apresentado a experiência de uma puérpera de alto risco que desejou participar e assinou o Termo de Consentimento Livre e Esclarecido. Resultados: Os resultados demonstram a mescla de sentimentos enfrentada pela puérpera de alto risco. Conclusão: Sendo importante a ampliação do termo Puerpério de Alto Risco nos programas de saúde, a fim de contemplar o cuidado de enfermagem específico às puérperas que estão com seus bebês na unidade neonatal.

  5. Thermal conductivity of BaPuO 3 at temperatures from 300 to 1500 K

    Science.gov (United States)

    Tanaka, Kosuke; Sato, Isamu; Hirosawa, Takashi; Kurosaki, Ken; Muta, Hiroaki; Yamanaka, Shinsuke

    2011-07-01

    Polycrystalline specimens of barium plutonate, BaPuO 3, have been prepared by mixing the appropriate amounts of PuO 2 and BaCO 3 followed by reacting and sintering at 1600 K under the flowing gas atmosphere of dry-air. The sintered specimens had a single phase of orthorhombic perovskite structure and were crack-free. The Debye temperature of BaPuO 3 was determined from the sound velocity and lattice parameter measurements. The elastic moduli were also determined from the longitudinal and shear sound velocity. The thermal conductivity of BaPuO 3 was calculated from the measured density at room temperature, literature values of heat capacity, and thermal diffusivity measured by a laser flash method in vacuum. The thermal conductivity of BaPuO 3 was roughly independent of the temperature and was almost the same magnitude as that of BaUO 3. This was markedly lower than the conductivities of other perovskite type oxides and was about one-tenth that of UO 2 around room temperature. The temperature dependence of the thermal conductivity of BaPuO 3 was found to be quite similar to that of BaUO 3.

  6. DNA methylation-mediated silencing of PU.1 in leukemia cells resistant to cell differentiation.

    Science.gov (United States)

    Fernández-Nestosa, María José; Monturus, Estefanía; Sánchez, Zunilda; Torres, Francisco S; Fernández, Agustín F; Fraga, Mario F; Hernández, Pablo; Schvartzman, Jorge B; Krimer, Dora B

    2013-01-01

    In mice, the proviral integration of the Friend Spleen Focus Forming Virus (SFFV) within the PU.1 locus of erythroid precursors results in the development of erythroleukemia. SFFV integrates several kilobases upstream of the PU.1 transcription initiation start site leading to the constitutive activation of the gene which in turn results in a block of erythroid differentiation. In this study we have mapped and sequenced the exact location of the retroviral integration site. We have shown that SFFV integrates downstream of a previously described upstream regulatory element (URE), precisely 2,976 bp downstream of the URE-distal element. We have also found that SFFV persists integrated within the same location in resistant cell lines that have lost their differentiation capacity and in which case PU.1 remains silent. We have examined the methylation status of PU.1 and found that in resistant cells the nearby CpG islands remained methylated in contrast to a non-methylated status of the parental cell lines. Treatment with 5-aza-2'-deoxycytidine caused resistant cells to differentiate yet only when combined with HMBA. Altogether these results strongly suggest that methylation plays a crucial role with regard to PU.1 silencing. However, although demethylation is required, it is not sufficient to overcome the differentiation impasse. We have also showed that activation blockage of the Epo/Epo-R pathway remains despite of the absence of PU.1.

  7. Conversion electron spectrometry of Pu isotopes with a silicon drift detector.

    Science.gov (United States)

    Pommé, S; Paepen, J; Peräjärvi, K; Turunen, J; Pöllänen, R

    2016-03-01

    An electron spectrometry set-up was built at IRMM consisting of a vacuum chamber with a moveable source holder and windowless Peltier-cooled silicon drift detector (SDD). The SDD is well suited for measuring low-energy x rays and electrons emitted from thin radioactive sources with low self-absorption. The attainable energy resolution is better than 0.5keV for electrons of 30keV. It has been used to measure the conversion electron spectra of three plutonium isotopes, i.e. (238)Pu, (239)Pu, (240)Pu, as well as (241)Am (being a decay product of (241)Pu). The obtained mixed x-ray and electron spectra are compared with spectra obtained with a close-geometry set-up using another SDD in STUK and spectra measured with a Si(Li) detector at IRMM. The potential of conversion electron spectrometry for isotopic analysis of mixed plutonium samples is investigated. With respect to the (240)Pu/(239)Pu isotopic ratio, the conversion electron peaks of both isotopes are more clearly separated than their largely overlapping peaks in alpha spectra.

  8. Determination of Pu-238 Abundance in a Plutonium Standard by an Advanced Thermal Ionization Mass Spectrometric Technique

    Science.gov (United States)

    Mason, P.; Thomas, R.

    2006-12-01

    New developments in thermal ionization mass spectrometers allow for the determination of very small minor isotope ratios. The new hardware and software capabilities require attention to detail and accounting for additional sources of measurement uncertainty. The Pu-238 isotopic composition in New Brunswick Laboratory plutonium metal standard CRM 126-A was determined by thermal ionization mass spectrometry using combined Faraday cup and ion counting detection. A dynamic acquisition scheme was employed which provided for near real-time mass fractionation correction and ion counter/Faraday detector inter-calibration. Steps taken to minimize or eliminate isobaric U-238 interferences will be described, and an evaluation detailing contributions to the uncertainty, including SEM non-linearity, will be presented.

  9. Hematological responses after inhaling {sup 238}PuO{sub 2}: An extrapolation from beagle dogs to humans

    Energy Technology Data Exchange (ETDEWEB)

    Scott, B.R.; Muggenburg, B.A.; Welsh, C.A.; Angerstein, D.A.

    1994-11-01

    The alpha emitter plutonium-238 ({sup 238}Pu), which is produced in uranium-fueled, light-water reactors, is used as a thermoelectric power source for space applications. Inhalation of a mixed oxide form of Pu is the most likely mode of exposure of workers and the general public. Occupational exposures to {sup 238}PuO{sub 2} have occurred in association with the fabrication of radioisotope thermoelectric generators. Organs and tissue at risk for deterministic and stochastic effects of {sup 238}Pu-alpha irradiation include the lung, liver, skeleton, and lymphatic tissue. Little has been reported about the effects of inhaled {sup 238}PuO{sub 2} on peripheral blood cell counts in humans. The purpose of this study was to investigate hematological responses after a single inhalation exposure of Beagle dogs to alpha-emitting {sup 238}PuO{sub 2} particles and to extrapolate results to humans.

  10. Multiple DNA-binding modes for the ETS family transcription factor PU.1.

    Science.gov (United States)

    Esaki, Shingo; Evich, Marina G; Erlitzki, Noa; Germann, Markus W; Poon, Gregory M K

    2017-09-29

    The eponymous DNA-binding domain of ETS (E26 transformation-specific) transcription factors binds a single sequence-specific site as a monomer over a single helical turn. Following our previous observation by titration calorimetry that the ETS member PU.1 dimerizes sequentially at a single sequence-specific DNA-binding site to form a 2:1 complex, we have carried out an extensive spectroscopic and biochemical characterization of site-specific PU.1 ETS complexes. Whereas 10 bp of DNA was sufficient to support PU.1 binding as a monomer, additional flanking bases were required to invoke sequential dimerization of the bound protein. NMR spectroscopy revealed a marked loss of signal intensity in the 2:1 complex, and mutational analysis implicated the distal surface away from the bound DNA as the dimerization interface. Hydroxyl radical DNA footprinting indicated that the site-specifically bound PU.1 dimers occupied an extended DNA interface downstream from the 5'-GGAA-3' core consensus relative to its 1:1 counterpart, thus explaining the apparent site size requirement for sequential dimerization. The site-specifically bound PU.1 dimer resisted competition from nonspecific DNA and showed affinities similar to other functionally significant PU.1 interactions. As sequential dimerization did not occur with the ETS domain of Ets-1, a close structural homolog of PU.1, 2:1 complex formation may represent an alternative autoinhibitory mechanism in the ETS family at the protein-DNA level. © 2017 by The American Society for Biochemistry and Molecular Biology, Inc.

  11. Minimum pickup velocity (U{sub pu}) of nanoparticles in gas–solid pneumatic conveying

    Energy Technology Data Exchange (ETDEWEB)

    Anantharaman, Aditya [Nanyang Technological University, School of Chemical and Biomedical Engineering (Singapore); Ommen, J. Ruud van [Delft University of Technology, Department of Chemical Engineering (Netherlands); Chew, Jia Wei, E-mail: JChew@ntu.edu.sg [Nanyang Technological University, School of Chemical and Biomedical Engineering (Singapore)

    2015-12-15

    This paper is the first systematic study of the pneumatic conveying of nanoparticles. The minimum pickup velocity, U{sub pu}, of six nanoparticle species of different materials [i.e., silicon dioxide (SiO{sub 2}), aluminum oxide (Al{sub 2}O{sub 3}), and titanium dioxide (TiO{sub 2})] and surfaces (i.e., apolar and polar) was determined by the weight loss method. Results show that (1) due to relative lack of hydrogen bonding, apolar nanoparticles had higher mass loss values at the same velocities, mass loss curves with accentuated S-shaped profiles, and lower U{sub pu} values, (2) among the three species, SiO{sub 2}, which has the lowest Hamaker coefficient, exhibited the greatest discrepancy between apolar and polar surfaces with respect to both mass loss curves and U{sub pu} values, (3) U{sub mf,polar}/U{sub mf,apolar} was between 1 and 3.5 times that of U{sub pu,polar}/U{sub pu,apolar} due to greater extents of hydrogen bonding associated with U{sub mf}, (4) U{sub pu} values were at least an order-of-magnitude lower than that expected from the well-acknowledged U{sub pu} correlation (Kalman et al., Powder Technol 160:103–113, 2005) due to agglomeration, (5) although nanoparticles should be categorized as Zone III (Kalman et al. 2005) (or Geldart group C, Powder Technol 7:285–292, 1973), the nanoparticles, and primary and complex agglomerates agreed more with the Zone I (or Geldart group B) correlation.

  12. Development of prototype induced-fission-based Pu accountancy instrument for safeguards applications.

    Science.gov (United States)

    Seo, Hee; Lee, Seung Kyu; An, Su Jung; Park, Se-Hwan; Ku, Jeong-Hoe; Menlove, Howard O; Rael, Carlos D; LaFleur, Adrienne M; Browne, Michael C

    2016-09-01

    Prototype safeguards instrument for nuclear material accountancy (NMA) of uranium/transuranic (U/TRU) products that could be produced in a future advanced PWR fuel processing facility has been developed and characterized. This is a new, hybrid neutron measurement system based on fast neutron energy multiplication (FNEM) and passive neutron albedo reactivity (PNAR) methods. The FNEM method is sensitive to the induced fission rate by fast neutrons, while the PNAR method is sensitive to the induced fission rate by thermal neutrons in the sample to be measured. The induced fission rate is proportional to the total amount of fissile material, especially plutonium (Pu), in the U/TRU product; hence, the Pu amount can be calibrated as a function of the induced fission rate, which can be measured using either the FNEM or PNAR method. In the present study, the prototype system was built using six (3)He tubes, and its performance was evaluated for various detector parameters including high-voltage (HV) plateau, efficiency profiles, dead time, and stability. The system's capability to measure the difference in the average neutron energy for the FNEM signature also was evaluated, using AmLi, PuBe, (252)Cf, as well as four Pu-oxide sources each with a different impurity (Al, F, Mg, and B) and producing (α,n) neutrons with different average energies. Future work will measure the hybrid signature (i.e., FNEM×PNAR) for a Pu source with an external interrogating neutron source after enlarging the cavity size of the prototype system to accommodate a large-size Pu source (~600g Pu).

  13. Goethite colloid enhanced Pu transport through a single saturated fracture in granite.

    Science.gov (United States)

    Lin, Jianfeng; Dang, Haijun; Xie, Jinchuan; Li, Mei; Zhou, Guoqing; Zhang, Jihong; Zhang, Haitao; Yi, Xiaowei

    2014-08-01

    α-FeOOH, a stable iron oxide in nature, can strongly absorb the low-solubility plutonium (Pu) in aquifers. However, whether Pu transports though a single saturated fracture can be enhanced in the presence of α-FeOOH colloids remains unknown. Experimental studies were carried out to evaluate Pu mobilization at different water flow velocity, as affected by goethite colloids with various concentrations. Goethite nanorods were used to prepare (α-FeOOH)-associated Pu suspensions with α-FeOOH concentration of (0-150) mgL(-1). The work experimentally evidenced that α-FeOOH colloid does enhance transport of Pu through fractured granites. The fraction of mobile (239)Pu (RPu, m=41.5%) associated with the α-FeOOH of an extremely low colloid concentration (0.2mgL(-1)) is much larger than that in absence of α-FeOOH (RPu, m=6.98%). However, plutonium mobility began to decrease when α-FeOOH concentration was increased to 1.0mgL(-1). On the other hand, the fraction of mobile Pu increased gradually with the water flow velocity. Based on the experimental data, the mechanisms underlying the (α-FeOOH)-associated plutonium transport are comprehensively discussed in view of its dynamic deposition onto the granite surfaces, which is decided mainly by the relative interaction between the colloid particle and the immobile surface. This interaction is a balance of electrostatic force (may be repulsive or attractive), the van der Walls force, and the shear stress of flow.

  14. Fabrication process for sintered mixed oxides soluble in nitric acid from nitrate solutions. [nuclear fuels]. Procede d'obtention d'oxydes mixtes frittes solubles dans l'acide nitrique a partir de solutions de nitrates

    Energy Technology Data Exchange (ETDEWEB)

    Bachelard, R.; Germanaz, P.

    1987-10-02

    Mixed oxide nuclear fuels are obtained by mixing the nitrate solutions, concentration, heat treatment for an intermediary mixed oxide containing U(VI) and Pu(IV or VI), calcination to obtain U/sub 3/O/sub 8/, reduction in U(IV) and Pu(IV), pelletizing, sintering and machining. Less wastes are produced and the fuel pellets are soluble in nitric acid.

  15. Determination of 241Pu in nuclear waste slurries: a comparative study using LSC and ICP-MS.

    Science.gov (United States)

    Jäggi, M; Röllin, S; Alvarado, J A Corcho; Eikenberg, J

    2012-02-01

    (241)Pu was determined in slurry samples from a nuclear reactor decommissioning project at the Paul Scherrer Institute (Switzerland). To validate the results, the (241)Pu activities of five samples were determined by LSC (TriCarb and Quantulus) and ICP-MS, with each instrument at a different laboratory. In lack of certified reference materials for (241)Pu, the methods were further validated using the (241)Pu information values of two reference sediments (IAEA-300 and IAEA-384). Excellent agreement with the results was found between LSC and ICP-MS in the nuclear waste slurries and the reference sediments.

  16. {\\alpha}-accompanied cold ternary fission of $^{238-244}$Pu isotopes in equatorial and collinear configuration

    CERN Document Server

    Santhosh, K P; Priyanka, B

    2015-01-01

    The cold ternary fission of $^{238}$Pu, $^{240}$Pu, $^{242}$Pu and $^{244}$Pu isotopes, with $^{4}$He as light charged particle, in equatorial and collinear configuration has been studied within the Unified ternary fission model (UTFM). The fragment combination $^{100}$Zr+$^{4}$He+$^{134}$Te possessing the near doubly magic nuclei $^{134}$Te (N=82, Z=52) gives the highest yield in the alpha accompanied ternary fission of $^{238}$Pu. For the alpha accompanied ternary fission of $^{240}$Pu, $^{242}$Pu and $^{244}$Pu isotopes, the highest yield was found for the fragment combination with doubly magic nuclei $^{132}$Sn (N=82, Z=50) as the heavier fragment. The deformation and orientation of fragments have also been taken into account for the alpha accompanied ternary fission of $^{238-244}$Pu isotopes, and it has been found that in addition to closed shell effect, ground state deformation also plays an important role in determining the isotopic yield in the ternary fission process. The emission probability and ki...

  17. Distribution and source of (129)I, (239)(,240)Pu, (137)Cs in the environment of Lithuania.

    Science.gov (United States)

    Ežerinskis, Ž; Hou, X L; Druteikienė, R; Puzas, A; Šapolaitė, J; Gvozdaitė, R; Gudelis, A; Buivydas, Š; Remeikis, V

    2016-01-01

    Fifty five soil samples collected in the Lithuania teritory in 2011 and 2012 were analyzed for (129)I, (137)Cs and Pu isotopes in order to investigate the level and distribution of artificial radioactivity in Lithuania. The activity and atomic ratio of (238)Pu/((239,24)0)Pu, (129)I/(127)I and (131)I/(137)Cs were used to identify the origin of these radionuclides. The (238)Pu/(239+240)Pu and (240)Pu/(239)Pu ratios in the soil samples analyzed varied in the range of 0.02-0.18 and 0.18-0.24, respectively, suggesting the global fallout as the major source of Pu in Lithuania. The values of 10(-9) to 10(-6) for (129)I/(127)I atomic ratio revealed that the source of (129)I in Lithuania is global fallout in most cases though several sampling sites shows a possible impact of reprocessing releases. Estimated (129)I/(131)I ratio in soil samples from the southern part of Lithuania shows negligible input of the Chernobyl fallout. No correlation of the (137)Cs and Pu isotopes with (129)I was observed, indicating their different sources terms. Results demonstrate uneven distribution of these radionuclides in the Lithuanian territory and several sources of contamination i.e. Chernobyl accident, reprocessing releases and global fallout.

  18. The differentiation effect of low-dose cytosine arabinoside is disturbed in PU.1-knockdown K562 cells.

    Science.gov (United States)

    Nakano, Hiroko; Yanagita, Akane; Takahashi, Shinichiro

    2014-07-01

    We recently demonstrated by using PU.1-knockdown K562 (K562 PU.1KD) cells stably expressing PU.1 short inhibitory RNAs and PU.1-overexpressing K562 (K562 PU.1OE) cells, that therapeutic concentrations of 5-aza-2'-deoxycytidine (5-azadC) induce erythroid differentiation of these cells and that the PU.1 expression level is closely associated with the differentiating and apoptotic effects of 5-azadC on K562 cells. In this study, we investigated whether the effects of low-dose cytosine arabinoside (Ara-C), which is another erythroid differentiation inducer in K562 cells, is associated with the expression level of PU.1 in these cells. As a result, we demonstrated that the effect of Ara-C on cell viability and differentiation, as determined by the WST-8 assay and β-globin mRNA expression analysis, respectively, was suppressed in K562 PU.1KD cells compared to their controls. Collectively, these findings suggest that sufficient expression of PU.1 is indispensable for the erythroid differentiation of K562 cells.

  19. The Runx-PU.1 pathway preserves normal and AML/ETO9a leukemic stem cells.

    Science.gov (United States)

    Staber, Philipp B; Zhang, Pu; Ye, Min; Welner, Robert S; Levantini, Elena; Di Ruscio, Annalisa; Ebralidze, Alexander K; Bach, Christian; Zhang, Hong; Zhang, Junyan; Vanura, Katrina; Delwel, Ruud; Yang, Henry; Huang, Gang; Tenen, Daniel G

    2014-10-01

    Runx transcription factors contribute to hematopoiesis and are frequently implicated in hematologic malignancies. All three Runx isoforms are expressed at the earliest stages of hematopoiesis; however, their function in hematopoietic stem cells (HSCs) is not fully elucidated. Here, we show that Runx factors are essential in HSCs by driving the expression of the hematopoietic transcription factor PU.1. Mechanistically, by using a knockin mouse model in which all three Runx binding sites in the -14kb enhancer of PU.1 are disrupted, we observed failure to form chromosomal interactions between the PU.1 enhancer and its proximal promoter. Consequently, decreased PU.1 levels resulted in diminished long-term HSC function through HSC exhaustion, which could be rescued by reintroducing a PU.1 transgene. Similarly, in a mouse model of AML/ETO9a leukemia, disrupting the Runx binding sites resulted in decreased PU.1 levels. Leukemia onset was delayed, and limiting dilution transplantation experiments demonstrated functional loss of leukemia-initiating cells. This is surprising, because low PU.1 levels have been considered a hallmark of AML/ETO leukemia, as indicated in mouse models and as shown here in samples from leukemic patients. Our data demonstrate that Runx-dependent PU.1 chromatin interaction and transcription of PU.1 are essential for both normal and leukemia stem cells.

  20. 46 CFR 154.421 - Allowable stress.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Allowable stress. 154.421 Section 154.421 Shipping COAST... § 154.421 Allowable stress. The allowable stress for the integral tank structure must meet the American Bureau of Shipping's allowable stress for the vessel's hull published in “Rules for Building and Classing...

  1. 46 CFR 154.440 - Allowable stress.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Allowable stress. 154.440 Section 154.440 Shipping COAST... Tank Type A § 154.440 Allowable stress. (a) The allowable stresses for an independent tank type A must... Commandant (CG-522). (b) A greater allowable stress than required in paragraph (a)(1) of this section may be...

  2. First-Principles Study of Structural, Magnetic, Electronic and Elastic Properties of PuC2

    Science.gov (United States)

    Yang, Rong; Tang, Bin; Gao, Tao; Ao, Bing-Yun

    2016-10-01

    We perform first-principles calculations of crystal structure, magnetism, electronic structure, chemical bonding and elastic properties for PuC2 using the standard local spin-density approximation (LSDA)+U scheme. The use of the Hubbard term to describe the 5f electrons of plutonium is discussed according to the lattice parameters, magnetism and densities of states. Our calculated lattice constants and magnetism are in good agreement with the experimental data or other theoretical calculations. It is shown that the total densities of states at the Fermi energy level mainly come from the contribution of narrow f band. The Pu-C bonds of PuC2 have a mixture of covalent character and ionic character, while covalent character is stronger than ionic character. The C1-C2 bonding has strong covalent character because of sp2 hybridization between C atoms. Lastly, the elastic properties of PuC2 are studied. We hope that our results can provide a useful reference for further theoretical and experimental research on PuC2. Supported by the National Natural Science Foundation of China under Grant Nos. 21371160, 21401173, and the Science Challenge Program of China

  3. Design of BPM PU for Low-Beta Proton Beam Using Magic Code

    CERN Document Server

    Park, S J; Bae, Y S; Hwang, W H; Huang, J Y; Nam, S H

    2003-01-01

    We have designed the BPM PU based on capacitive buttons for use in the KOMAC (Korea Multi-purpose Accelerator Complex), the high-intensity proton linac that are under development at the KAERI (Korea Atomic Research Institute), Korea. The KOMAC is aiming to produce CW 20 mA beam current at the 100 MeV energy. We have chosen the button-type PU since it is easier to fabricate than other type PUs including the stripline, and it could provide enough signal power because of the high beam current. The PU sensitivity was calculated by the MAGIC that is a kind of the Particle-In-Cell code that originates from the plasma science community. The utilization of the MAGIC code is especially useful for BPM PUs in the low-beta sections of the accelerator, because it is difficult to obtain the PU sensitivity experimentally due to the difficulties in simulating the low-beta beams by the electromagnetic waves in a test bench. In this presentation, we report on the design of the BPM PU based on the MAGIC calculation.

  4. Structure and phase stability of a Pu-0.32 wt% Ga alloy

    Science.gov (United States)

    Wheeler, D. W.; Ennaceur, S. M.; Matthews, M. B.; Roussel, P.; Bayer, P. D.

    2016-08-01

    In plutonium-gallium (Pu-Ga) alloys that have a Ga content of 0.3-0.4 wt%, their readiness to transform to α‧ renders them of particular interest in efforts to understand the tenuous nature of δ phase stability. The present study is a comprehensive examination of the structure and phase stability of a cast Pu-0.32 wt% Ga alloy, the Ga content being close to the minimum amount needed to retain the δ phase to ambient temperature. The alloy was characterised in both the as-cast condition as well as following a homogenising heat treatment. The 250-h heat treatment at 450 °C was shown to achieve an apparently stable δ-Pu phase. However, the stability of the δ-Pu phase was shown to be marginal: partial transformation to α‧-Pu was observed when the alloy was subjected to hydrostatic compression. Similar transformation was also apparent during metallographic preparation as well as during hardness indentation. The results provide new understanding of the nature of δ phase stability.

  5. DENSITY-FUNCTIONAL CALCULATIONS FOR Ce, Th, AND Pu METALS AND ALLOYS

    Energy Technology Data Exchange (ETDEWEB)

    Landa, A; Soderlind, P

    2004-04-05

    The phase diagrams of Ce, Th, and Pu metals have been studied by means of density-functional theory (DFT). In addition to these metals, the phase stability of Ce-Th and Pu-Am alloys has been also investigated from first-principles calculations. Equation-of-state (EOS) for Ce, Th, and the Ce-Th alloys has been calculated up to 1 Mbar pressure in good comparison to experimental data. Present calculations shows that the Ce-Th alloys adopt a body-centeredtetragonal (bct) structure upon hydrostatic compression that is in excellent agreement with measurements. The ambient pressure phase diagram of Pu is shown to be very poorly described by traditional DFT but rather well modeled when including magnetic interactions. In particular, the anomalous {var_sigma} phase of Pu is shown to be stabilized by magnetic disorder at elevated temperatures. The Pu-Am system has also been studied in a similar fashion and it is shown that this system, for about 25% Am content, becomes antiferromagnetic below about 400 K that corroborate the recent discovery of a Curie-Weiss behavior in this system.

  6. Extension of 239+240Pu sediment geochronology to coarse-grained marine sediments

    Science.gov (United States)

    Kuehl, Steven A.; Ketterer, Michael E.; Miselis, Jennifer L.

    2012-01-01

    Sediment geochronology of coastal sedimentary environments dominated by sand has been extremely limited because concentrations of natural and bomb-fallout radionuclides are often below the limit of measurement using standard techniques. ICP-MS analyses of 239+240Pu from two sites representative of traditionally challenging (i.e., low concentration) environments provide a "proof of concept" and demonstrate a new application for bomb-fallout radiotracers in the study of sandy shelf-seabed dynamics. A kasten core from the New Zealand shelf in the Southern Hemisphere (low fallout), and a vibracore from the sandy nearshore of North Carolina (low particle surface area) both reveal measurable 239+240Pu activities at depth. In the case of the New Zealand site, independently verified steady-state sedimentation results in a 239+240Pu profile that mimics the expected atmospheric fallout. The depth profile of 239+240Pu in the North Carolina core is more uniform, indicating significant sediment resuspension, which would be expected in this energetic nearshore environment. This study, for the first time, demonstrates the utility of 239+240Pu in the study of sandy environments, significantly extending the application of bomb-fallout isotopes to coarse-grained sediments, which compose the majority of nearshore regions.

  7. Roles of RUNX1 and PU.1 in CCR3 Transcription.

    Science.gov (United States)

    Kong, Su-Kang; Kim, Byung Soo; Hwang, Sae Mi; Lee, Hyune Hwan; Chung, Il Yup

    2016-06-01

    CCR3 is a chemokine receptor that mediates the accumulation of allergic inflammatory cells, including eosinophils and Th2 cells, at inflamed sites. The regulatory sequence of the CCR3 gene, contains two Runt-related transcription factor (RUNX) 1 sites and two PU.1 sites, in addition to a functional GATA site for transactivation of the CCR3 gene. In the present study, we examined the effects of the cis-acting elements of RUNX1 and PU.1 on transcription of the gene in EoL-1 eosinophilic cells and Jurkat T cells, both of which expressed functional surface CCR3 and these two transcription factors. Introduction of RUNX1 siRNA or PU.1 siRNA resulted in a modest decrease in CCR3 reporter activity in both cell types, compared with transfection of GATA-1 siRNA. Cotransfection of the two siRNAs led to inhibition in an additive manner. EMSA analysis showed that RUNX1, in particular, bound to its binding motifs. Mutagenesis analysis revealed that all point mutants lacking RUNX1- and PU.1-binding sites exhibited reduced reporter activities. These results suggest that RUNX1 and PU.1 participate in transcriptional regulation of the CCR3 gene.

  8. DENSITY-FUNCTIONAL CALCULATIONS FOR Ce, Th, AND Pu METALS AND ALLOYS

    Directory of Open Access Journals (Sweden)

    A.Landa

    2004-01-01

    Full Text Available The phase diagrams of Ce, Th, and Pu metals have been studied by means of density-functional theory (DFT. In addition to these metals, the phase stability of Ce-Th and Pu-Am alloys has been also investigated from first-principles calculations. Equation-of-state (EOS for Ce, Th, and the Ce-Th alloys has been calculated up to 1 Mbar pressure in good comparison to experimental data. Present calculations show that the Ce-Th alloys adopt a body-centered-tetragonal (bct structure upon hydrostatic compression which is in excellent agreement with measurements. The ambient pressure phase diagram of Pu is shown to be very poorly described by traditional DFT but rather well modelled when including magnetic interactions. In particular, the anomalous δ phase of Pu is shown to be stabilized by magnetic disorder at elevated temperatures. The Pu-Am system has also been studied in a similar fashion and it is shown that this system, for about 25% Am content, becomes antiferromagnetic below about 400 K which corroborates the recent discovery of a Curie-Weiss behavior in this system.

  9. Plutonium {sup 241}Pu in tissues and organs of Cervidae from Northern Poland

    Energy Technology Data Exchange (ETDEWEB)

    Struminska-Parulska, Dagmara I.; Skwarzec, Bogdan [Gdansk Univ. (Poland). Dept. of Environmental Chemistry and Radiochemistry

    2015-07-01

    Livers, kidneys and muscles of large herbivorous animals: roe deer, red deer and fallow deer, collected in Northern Poland, were the subject of the investigation. The concentration of {sup 241}Pu ranged widely between 1.31 ± 0.28 and 214.5 ± 25.8 mBq kg{sup -1} ww and decreased in the order kidney > liver > muscle. The average values of the activity concentrations of {sup 241}Pu were 11.5 ± 1.8 mBq kg{sup -1} ww in muscles, 14.0 ± 2.25 mBq kg{sup -1} ww in liver and 85.5 ± 9.7 mBq kg{sup -1} ww in kidneys. As statistically checked the sampling location, sex, age and species of animals did not influence on plutonium concentrations of the analyzed samples. Only the organ type significantly influenced {sup 241}Pu content. The values of {sup 241}Pu/{sup 29+240}Pu activity ratio in analyzed samples ranged from 7.12 ± 2.15 to 99.3 ± 16.4 and the results showed the main source of plutonium in analyzed organs could be the Chernobyl accident.

  10. Simultaneous determination of radiocesium ((135)Cs, (137)Cs) and plutonium ((239)Pu, (240)Pu) isotopes in river suspended particles by ICP-MS/MS and SF-ICP-MS.

    Science.gov (United States)

    Cao, Liguo; Zheng, Jian; Tsukada, Hirofumi; Pan, Shaoming; Wang, Zhongtang; Tagami, Keiko; Uchida, Shigeo

    2016-10-01

    Due to radioisotope releases in the Fukushima Dai-ichi Nuclear Power Plant (FDNPP) accident, long-term monitoring of radiocesium ((135)Cs and (137)Cs) and Pu isotopes ((239)Pu and (240)Pu) in river suspended particles is necessary to study the transport and fate of these long-lived radioisotopes in the land-ocean system. However, it is expensive and technically difficult to collect samples of suspended particles from river and ocean. Thus, simultaneous determination of multi-radionuclides remains as a challenging topic. In this study, for the first time, we report an analytical method for simultaneous determination of radiocesium and Pu isotopes in suspended particles with small sample size (1-2g). Radiocesium and Pu were sequentially pre-concentrated using ammonium molybdophosphate and ferric hydroxide co-precipitation, respectively. After the two-stage ion-exchange chromatography separation from the matrix elements, radiocesium and Pu isotopes were finally determined by ICP-MS/MS and SF-ICP-MS, respectively. The interfering elements of U ((238)U(1)H(+) and (238)U(2)H(+) for (239)Pu and (240)Pu, respectively) and Ba ((135)Ba(+) and (137)Ba(+) for (135)Cs and (137)Cs, respectively) were sufficiently removed with the decontamination factors of 1-8×10(6) and 1×10(4), respectively, with the developed method. Soil reference materials were utilized for method validation, and the obtained (135)Cs/(137)Cs and (240)Pu/(239)Pu atom ratios, and (239+240)Pu activities showed a good agreement with the certified/information values. In addition, the developed method was applied to analyze radiocesium and Pu in the suspended particles of land water samples collected from Fukushima Prefecture after the FDNPP accident. The (135)Cs/(137)Cs atom ratios (0.329-0.391) and (137)Cs activities (23.4-152Bq/g) suggested radiocesium contamination of the suspended particles mainly originated from the accident-released radioactive contaminates, while similar Pu contamination of suspended

  11. STRONTIUM AND ACTINIDE SEPARATIONS FROM HIGH LEVEL NUCLEAR WASTE SOLUTIONS USING MONOSODIUM TITANATE 1. SIMULANT TESTING

    Energy Technology Data Exchange (ETDEWEB)

    HOBBS, D. T.; BARNES, M. J.; PULMANO, R. L.; MARSHALL, K. M.; EDWARDS, T. B.; BRONIKOWSKI, M. G.; FINK, S. D.

    2005-04-14

    High-level nuclear waste produced from fuel reprocessing operations at the Savannah River Site (SRS) requires pretreatment to remove {sup 137}Cs, {sup 90}Sr and alpha-emitting radionuclides (i.e., actinides) prior to disposal. Separation processes planned at SRS include caustic side solvent extraction, for {sup 137}Cs removal, and ion exchange/sorption of {sup 90}Sr and alpha-emitting radionuclides with an inorganic material, monosodium titanate (MST). The predominant alpha-emitting radionuclides in the highly alkaline waste solutions include plutonium isotopes {sup 238}Pu, {sup 239}Pu and {sup 240}Pu. This paper provides a summary of data acquired to measure the performance of MST to remove strontium and actinides from simulated waste solutions. These tests evaluated the influence of ionic strength, temperature, solution composition and the oxidation state of plutonium.

  12. Influence of Salts on Electrospinning of Aqueous and Nonaqueous Polymer Solutions

    Directory of Open Access Journals (Sweden)

    Fatma Yalcinkaya

    2015-01-01

    Full Text Available A roller electrospinning system was used to produce nanofibres by using different solution systems. Although the process of electrospinning has been known for over half a century, knowledge about spinning behaviour is still lacking. In this work, we investigated the effects of salt for two solution systems on spinning performance, fibre diameter, and web structure. Polyurethane (PU and polyethylene oxide (PEO were used as polymer, and tetraethylammonium bromide and lithium chloride were used as salt. Both polymer and salt concentrations had a noteworthy influence on the spinning performance, morphology, and diameter of the nanofibres. Results indicated that adding salt increased the spinnability of PU. Salt created complex bonding with dimethylformamide solvent and PU polymer. Salt added to PEO solution decreased the spinning performance of fibres while creating thin nanofibres, as explained by the leaky dielectric model.

  13. Analysis on the Isotopic Ratio of Picogram Pu by TIMS%皮克量级钚同位素丰度比的TIMS分析

    Institute of Scientific and Technical Information of China (English)

    杨天丽; 龙开明; 刘雪梅; 刘钊; 汤磊

    2005-01-01

    The isotopic abundance ratios for Pu at 6.7 pg level were measured by thermal surface ionization mass spectrometry (TIMS). During the preparation of Pu samples carbon power was used as an emitting and stabilizing reagent, which increase the collection efficiency, the ion current intense and the ion emission stability for Pu. The measurment results indicate that the relative standard deviation of 2.7% for the isotopic abundance ratios of 240Pu to 239Pu is achieved when the 240Pu ion current is 8-20 cps.

  14. Oxygen diffusion model of the mixed (U,Pu)O2 ± x: Assessment and application

    Science.gov (United States)

    Moore, Emily; Guéneau, Christine; Crocombette, Jean-Paul

    2017-03-01

    The uranium-plutonium (U,Pu)O2 ± x mixed oxide (MOX) is used as a nuclear fuel in some light water reactors and considered for future reactor generations. To gain insight into fuel restructuring, which occurs during the fuel lifetime as well as possible accident scenarios understanding of the thermodynamic and kinetic behavior is crucial. A comprehensive evaluation of thermo-kinetic properties is incorporated in a computational CALPHAD type model. The present DICTRA based model describes oxygen diffusion across the whole range of plutonium, uranium and oxygen compositions and temperatures by incorporating vacancy and interstitial migration pathways for oxygen. The self and chemical diffusion coefficients are assessed for the binary UO2 ± x and PuO2 - x systems and the description is extended to the ternary mixed oxide (U,Pu)O2 ± x by extrapolation. A simulation to validate the applicability of this model is considered.

  15. Transport and scavenging of Pu in surface waters of the Southern Hemisphere Oceans

    DEFF Research Database (Denmark)

    Gastaud, J.; Povinec, P.P.; Aoyama, M.

    2011-01-01

    The distribution of 239Pu in Atlantic and Indian Ocean waters about four decades after their main injection from atmospheric nuclear weapons tests is discussed. Recent data obtained in the framework of the SHOTS (Southern Hemisphere Ocean Tracer Studies) projects are evaluated and compared...... with previous investigations. Seawater samples were collected during the round the globe BEAGLE2003 (Blue Ocean Global Expedition) along the 30°S transect in the Atlantic and the 20°S transect in the Indian Ocean. The results indicate transport of surface waters labelled with 239Pu from the western North...... Pacific via the Indonesian Seas to the South Indian Ocean and then to the South Atlantic Ocean. Along the whole BEAGLE2003 sampling route, the Atlantic Ocean has the lowest 239Pu content due to its particle scavenging on the long way from the western North Pacific. On the other hand, concentrations...

  16. Simultaneous determination of free amino acids in Pu-erh tea and their changes during fermentation.

    Science.gov (United States)

    Zhu, Yuchen; Luo, Yinghua; Wang, Pengpu; Zhao, Mengyao; Li, Lei; Hu, Xiaosong; Chen, Fang

    2016-03-01

    Pu-erh ripened tea is produced through a unique microbial fermentation process from the sun-dried leaves of large-leaf tea species (Camellia sinensis (Linn.) var. assamica (Masters) Kitamura) in Yunnan province of China. In this study, the changes of amino acid profiles during fermentation of Pu-erh tea were investigated, based on the improved HPLC-UV method with PITC pre-column derivatization for the simultaneous determination of twenty free amino acids. Results showed that aspartic acid, glutamic acid, arginine, alanine, theanine and tyrosine were the major amino acids in tea samples. Fermentation significantly influenced on the amino acid profiles. The total free amino acid contents significantly decreased during fermentation (pamino acids and acrylamide contents in Pu-erh ripened tea.

  17. Kzp Regulates the Transcription of gata2 and pu.1 during Primitive Hematopoiesis in Zebrafish Embryos

    Institute of Scientific and Technical Information of China (English)

    Fang Liu; Shaohua Yao; Ting Zhang; Chun Xiao; Yanna Shang; Jin Liu; Xianming Mo

    2012-01-01

    Kaiso zinc finger-containing protein (Kzp),a maternally-derived transcription factor,controls dorsoventral patterning during zebrafish gastrulation.Here,we uncovered a new function for Kzp in zebrafish embryonic primitive hematopoiesis.The depletion of kzp led to defects in primitive hematopoiesis including the development of the erythroid and myeloid lineages.On the other hand,overexpression of kzp caused the ectopic expression of gatal,gata2,and pu.1.Chromosome immunoprecipitation assays revealed that Kzp protein directly binds to gatal,gata2,and pu.1 promoters.Interestingly,the ectopic expression of gata2 was able to rescue the erythroid,but not the myeloid lineage in kzp-depleted zebrafish embryos.gatal expression controlled by Kzp was dependent on gata2 during primitive erythropoiesis.Our results indicate that Kzp is a critical transcriptional factor for the expression of gata2 and pu.1 to modulate primitive hematopoiesis.

  18. Validation of new {sup 240}Pu cross section and covariance data via criticality calculation

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Do Heon; Gil, Choong-Sup; Kim, Hyeong Il; Lee, Young-Ouk, E-mail: kimdh@kaeri.re.kr, E-mail: csgil@kaeri.re.kr, E-mail: hikim@kaeri.re.kr, E-mail: yolee@kaeri.re.kr [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of); Leal, Luiz C.; Dunn, Michael E., E-mail: leallc@ornl.gov, E-mail: dunnme@ornl.gov [Oak Ridge National Laboratory, TN (United States)

    2011-07-01

    Recent collaboration between KAERI and ORNL has completed an evaluation for {sup 240}Pu neutron cross section with covariance data. The new {sup 240}Pu cross section data has been validated through 28 criticality safety benchmark problems taken from the ICSBEP and/or CSEWG specifications with MCNP calculations. The calculation results based on the new evaluation have been compared with those based on recent evaluations such as ENDF/B-VII.0, JEFF-3.1.1, and JENDL-4.0. In addition, the new {sup 240}Pu covariance data has been tested for some criticality benchmarks via the DANTSYS/SUSD3D-based nuclear data sensitivity and uncertainty analysis of k{sub eff}. The k{sub eff} uncertainty estimates by the new covariance data has been compared with those by JENDL-4.0, JENDL-3.3, and Low-Fidelity covariance data. (author)

  19. High temperature heat capacity of PuPO{sub 4} monazite-analogue

    Energy Technology Data Exchange (ETDEWEB)

    Benes, Ondrej, E-mail: ondrej.benes@ec.europa.eu [European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O. Box 2340, 76125 Karlsruhe (Germany); Popa, Karin [' Al.I. Cuza' University, Department of Chemistry, 11-Carol I Blvd., 700506 Iasi (Romania); Reuscher, Vivien [European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O. Box 2340, 76125 Karlsruhe (Germany); Physikalisch-Chemisches Institut, Ruprecht-Karls-Universitaet Heidelberg, Im Neuenheimer Feld 253, 69120 Heidelberg (Germany); Zappia, Alessandro; Staicu, Dragos; Konings, Rudy J.M. [European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O. Box 2340, 76125 Karlsruhe (Germany)

    2011-11-15

    Highlights: > The heat capacity of PuPO{sub 4} has been measured up to 1400 K. > Good agreement between the DSC and the drop technique has been found. > It was demonstrated that drop calorimetry is precise enough to measure relatively small samples. - Abstract: The enthalpy increments of PuPO{sub 4} have been measured using drop calorimetry in the temperature range from 530 K to 1386 K. The heat capacity was derived from the obtained data and compared with heat capacity data obtained directly from differential scanning calorimeter measured in this study from 400 K to 1400 K. The recommended heat capacity of PuPO{sub 4} was determined based on both techniques as: C{sub p}{sup 0}(JK{sup -1}mol{sup -1})=126.600+32.999x10{sup -3}(T/K)-1.9503x10{sup 6}(T/K){sup -2}.

  20. Efficient PU Mode Decision and Motion Estimation for H.264/AVC to HEVC Transcoder

    Directory of Open Access Journals (Sweden)

    Zong-Yi Chen

    2014-04-01

    Full Text Available H.264/AVC has been widely applied to various applications. However, a new video compression standard, High Efficient Video Coding (HEVC, had been finalized in 2013. In this work, a fast transcoder from H.264/AVC to HEVC is proposed. The proposed algorithm includes the fast prediction unit (PU decision and the fast motion estimation. With the strong relation between H.264/AVC and HEVC, the modes, residuals, and variance of motion vectors (MVs extracted from H.264/AVC can be reused to predict the current encoding PU of HEVC. Furthermore, the MVs from H.264/AVC are used to decide the search range of PU during motion estimation. Simulation results show that the proposed algorithm can save up to 53% of the encoding time and maintains the rate-distortion (R-D performance for HEVC.

  1. Similarities between Cu and Pu containing 'high T {sub c}' superconductors

    Energy Technology Data Exchange (ETDEWEB)

    Wachter, P. [Laboratorium fuer Festkoerperphysik, ETH Zuerich, 8093 Zurich (Switzerland)]. E-mail: wachter@solid.phys.ethz.ch

    2007-03-15

    PuCoGa{sub 5} has with 18.5 K an extremely high T {sub c} for superconductivity compared with other actinide materials having T{sub c}s around 2-3 K. It appears to be a 'high T {sub c} superconductor' in the field of actinides. After nearly 20 years of research in high T{sub c} superconductors, only Cu containing materials have T{sub c}s above about 30 K (exception MgB{sub 2}). BCS theory cannot explain such high transition temperatures, thus other or additional coupling mechanisms like magnetic exchange are necessary. Mixed valence, spin holes in an antiferromagnetic lattice, small energy difference between the various valences and two-dimensionality are common features of Cu and Pu containing superconductors. It can be shown in this paper that the mechanism for superconductivity is the same for Cu and Pu containing materials.

  2. Molecular Structure and Bonding in Plutonium Carbides: A Theoretical Study of PuC3.

    Science.gov (United States)

    Molpeceres, Germán; Rayón, Víctor M; Barrientos, Carmen; Largo, Antonio

    2016-04-14

    The most relevant species of plutonium tricarbide were characterized using theoretical methods. The global minimum is predicted to be a fan structure where the plutonium atom is bonded to a quasi-linear C3 unit. A rhombic isomer, shown to be a bicyclic species with transannular C-C bonding, lies about 39 kJ/mol above the fan isomer. A linear PuCCC isomer and a three-membered ring CPuC2 isomer were found to be higher in energy (150 and 195 kJ/mol, respectively, above the predicted global minimum). The possible processes for the formation of these species are discussed, and the IR spectra were predicted to help in possible experimental detection. The nature of the Pu-C interaction has been analyzed in terms of a topological analysis of the electronic density, showing that Pu-C bonding is essentially ionic with a certain degree of covalent character.

  3. Modeling and production of 240Am by deuteron-induced activation of a 240Pu target

    Energy Technology Data Exchange (ETDEWEB)

    Finn, Erin C.; McNamara, Bruce K.; Greenwood, Lawrence R.; Wittman, Richard S.; Soderquist, Chuck Z.; Woods, Vincent T.; VanDevender, Brent A.; Metz, Lori A.; Friese, Judah I.

    2015-02-01

    A novel reaction pathway for production of 240Am is reported. Models of reaction cross-sections in EMPIRE II suggests that deuteron-induced activation of a 240Pu target produces maximum yields of 240Am from 11.5 MeV incident deuterons. This activation had not been previously reported in the literature. A 240Pu target was activated under the modeled optimum conditions to produce 240Am. The modeled cross-section for the 240Pu(d, 2n)240Am reaction is on the order of 20-30 mbarn, but the experimentally estimated value is 5.3 ± 0.2 mbarn. We discuss reasons for the discrepancy as well as production of other Am isotopes that contaminate the final product.

  4. 238PuO2 Fuel and Dosimetry

    Energy Technology Data Exchange (ETDEWEB)

    Mayo, Douglas R. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Rawool-Sullivan, Mohini [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Garner, Scott Edward [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Wenz, Tracy R. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Karpius, Peter Joseph [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-06-01

    238Pu is an ideal material for use as a heat source with its half-life of 87.7 years and copious particle emissions. 238Pu radioisotope thermoelectric generators (RTGs) have found use for pacemakers, Apollo Space missions, Mars rovers, and Voyager spacecraft. In evaluating the dose to personnel and components near a 238Pu-based RTG, a number of additional nuclides and their daughter products must be considered to get an accurate estimate for γ-dose, and the amount of 17O and 18O for the neutron-dose must be considered. This paper looks at the contributing nuclides and their daughter products that add the most to the dose rates.

  5. Variability in PuO{sub 2} Intake by Inhalation: Implications for Worker Protection at the US Department of Energy

    Energy Technology Data Exchange (ETDEWEB)

    Scott, B.R.; Fencl, A.F

    1999-07-01

    This paper describes the stochastic exposure (SE) paradigm where, at most, small numbers of airborne toxic particles are presented for inhalation. The focus is on alpha-emitting plutonium dioxide (PuO{sub 2}) particles that may be inhaled by Department of Energy (DOE) workers. Consideration of the SE paradigm is important because intake of only a few highly radioactive PuO{sub 2} particles such as {sup 238}PuO{sub 2}, could greatly exceed the annual limit on intake (ALI) used to control worker exposure. For the SE paradigm, credible intake distributions evaluated over the population at risk are needed, rather than unreliable point estimates of intake. Credible distributions of radiation doses and health risks are also needed. Because there are limited data on humans who inhaled PuO{sub 2}, these distributions must be calculated. Calculated distributions are presented that relate to the intake of radioactivity via inhaling polydisperse PuO{sub 2} particles. The results indicate that a large variability in radioactivity intake is expected when relatively small numbers of PuO{sub 2} particles are inhaled. For the SE paradigm, one cannot know how many PuO{sub 2} particles were inhaled by an individual involved in a given inhalation exposure scenario. Thus, rather than addressing questions such as 'Did the calculated worker's intake of {sup 238}PuO{sub 2} exceed the ALI?', it is better to address questions such as 'What is the probability that {sup 238}PuO{sub 2} intake by a given worker occurred and exceeded the ALI?' Mathematical tools for addressing the latter question are presented, and examples of their applications are provided, with emphasis on possible DOE worker exposures at the Rocky Flats facility near Denver, Colorado. The alpha-emitting isotopes {sup 238}Pu, {sup 239}Pu, {sup 240}Pu and {sup 242}Pu are found at Rocky Flats. Although {sup 238}Pu is thought to be present in relatively small amounts there, intake via inhalation of only

  6. Runx1 regulation of Pu.1 corepressor/coactivator exchange identifies specific molecular targets for leukemia differentiation therapy.

    Science.gov (United States)

    Gu, Xiaorong; Hu, Zhenbo; Ebrahem, Quteba; Crabb, John S; Mahfouz, Reda Z; Radivoyevitch, Tomas; Crabb, John W; Saunthararajah, Yogen

    2014-05-23

    Gene activation requires cooperative assembly of multiprotein transcription factor-coregulator complexes. Disruption to cooperative assemblage could underlie repression of tumor suppressor genes in leukemia cells. Mechanisms of cooperation and its disruption were therefore examined for PU.1 and RUNX1, transcription factors that cooperate to activate hematopoietic differentiation genes. PU.1 is highly expressed in leukemia cells, whereas RUNX1 is frequently inactivated by mutation or translocation. Thus, coregulator interactions of Pu.1 were examined by immunoprecipitation coupled with tandem mass spectrometry/Western blot in wild-type and Runx1-deficient hematopoietic cells. In wild-type cells, the NuAT and Baf families of coactivators coimmunoprecipitated with Pu.1. Runx1 deficiency produced a striking switch to Pu.1 interaction with the Dnmt1, Sin3A, Nurd, CoRest, and B-Wich corepressor families. Corepressors of the Polycomb family, which are frequently inactivated by mutation or deletion in myeloid leukemia, did not interact with Pu.1. The most significant gene ontology association of Runx1-Pu.1 co-bound genes was with macrophages, therefore, functional consequences of altered corepressor/coactivator exchange were examined at Mcsfr, a key macrophage differentiation gene. In chromatin immunoprecipitation analyses, high level Pu.1 binding to the Mcsfr promoter was not decreased by Runx1 deficiency. However, the Pu.1-driven shift from histone repression to activation marks at this locus, and terminal macrophage differentiation, were substantially diminished. DNMT1 inhibition, but not Polycomb inhibition, in RUNX1-translocated leukemia cells induced terminal differentiation. Thus, RUNX1 and PU.1 cooperate to exchange corepressors for coactivators, and the specific corepressors recruited to PU.1 as a consequence of RUNX1 deficiency could be rational targets for leukemia differentiation therapy.

  7. Critical mass studies of plutonium solutions

    Energy Technology Data Exchange (ETDEWEB)

    Kruesi, F.E.; Erkman, J.O.; Lanning, D.D.

    1952-05-19

    The chain reacting conditions for plutonium nitrate in water solution have been examined experimentally for a variety of sizes of spheres and cylinders. The effects on the critical mass of the displacement of hydrogen and the addition of poisons to the fuel were measured in water tamped and bare reactors. In this report the data obtained in the investigation is presented graphically and in tables. Some preliminary analysis has been made yielding the results: (i) the absorption cross-section of Pu{sup 240} is 925 {plus_minus} 200 barns and (ii) the minimum critical mass of Pu{sup 239} in water is 510 grams at concentration of about 33 grams per liter.

  8. Safety analysis report for the /sup 238/PuO/sub 2/ fuel form facility

    Energy Technology Data Exchange (ETDEWEB)

    Angerman, C.L.; Bickford, D.F.; Gould, T.H. Jr.; Smith, P.K.

    1977-08-01

    The Plutonium Fuel Form (PuFF) Facility has been constructed at the Savannah River Plant to manufacture 30 to 60 kg/yr of /sup 238/Pu fuel forms for space power applications. This facility is located in the existing Building 235-F near the geographical center of the Savannah River Plant (SRP) site. Pilot production is scheduled to begin in July 1977, with full-scale production in April 1978. The process line of the facility consists of nine separate, interconnected shielded cells; five shielded wing cabinets or glove boxes; three hoods; and contained auxiliary equipment. These process enclosures will be, for the most part, under an atmosphere of recirculating inert gas. The products of the facility will be dense fuel forms manufactured from PuO/sub 2/ powder with a nominal isotopic composition of 80% /sup 238/Pu-20% /sup 239/Pu. This powder, made from calcined oxalate, has been produced safely at a rate of about 20 kg /sup 238/Pu/yr in the H-Area B-Line in Building 221-H for approximately ten years. This report describes design objectives, nature of operations, potential hazards and limiting factors, facility response to postulated accidents and failures, and environmental effects. The results of the analyses described in this report indicate that the facility has the capacity to prevent or sufficiently reduce accidents that represent potential risks to health and safety. The safety analysis in conjunction with process requirements provides the bases for Technical Standards for operation. The analysis also documents the degree of conformance of the facility design with the General Design Criteria - Plutonium Facilities and the Environmental Statement.

  9. Effect of ionic strength on complexation of Pu(IV) with humic acid

    Energy Technology Data Exchange (ETDEWEB)

    Szabo, G.; Guezi, J. [National Research Inst. for Radiobiology and Radiohygiene, Budapest (Hungary); Reiller, P. [Commissariat a l' Energie Atomique, CE Saclay, Nuclear Energy Div./DPC/SECR, Lab. de Speciation des Radionucleides et des Molecules, Gif-sur-Yvette (France); Miyajima, T. [Dept. of Chemistry, Saga Univ. (Japan); Bulman, R.A. [Radiation Protection Div., Health Protection Agency, Chilton, Didcot (United Kingdom)

    2010-07-01

    Successful geochemical modelling of the migration of radioactive materials, such as the transuranic elements, from nuclear waste repositories is dependent upon an understanding of their interaction with biogeopolymers such as humic acids, the most likely complexing agents in groundwaters. An established silica/humic acid composite has been evaluated as a model substrate for naturally occurring humate-coated minerals that are likely to be present in the vicinity of the repositories. The binding of Pu(IV), the highly likely oxidation station, by the silica/humic substrate was examined at pH 4 in the range 0.02 to 3.00 M NaClO{sub 4} by the titration method. Pu(IV)-humate conditional stability constants have been evaluated from data obtained from these experiments by using non-linear regression of binding isotherms. The results have been interpreted in terms of complexes of 1: 1 stoichiometry. Analysis of the complex formation dependency with ionic strength shows that the effect of ionic strength on humate complexation of Pu(IV) is not dramatically pronounced. The complexation constants are evaluated for the humate interaction with Pu{sup 4-} and Pu(OH){sub 3}{sup +}, at pH 4. The complexation constants are found, respectively, to be log{sup HA}{beta}{sup 0}(Pu{sup 4+}) = 16.6 {+-} 0.3 and log{beta}{sup 0}{sub 1.3.1} = 46.6 {+-} 2.3. The estimations through analogy from previous results a are in agreement with these new experimental data (orig.)

  10. Transmutation of 129I, 237Np, 238Pu, 239Pu, and 241Am using neutrons produced in target-blanket system `Energy plus Transmutation' by relativistic protons

    Indian Academy of Sciences (India)

    J Adam; K Katovsky; A Balabekyan; V G Kalinnikov; M I Krivopustov; H Kumawat; A A Solnyshkin; V I Stegailov; S G Stetsenko; V M Tsoupko-Sitnikov; W Westmeier

    2007-02-01

    Target-blanket facility `Energy + Transmutation' was irradiated by proton beam extracted from the Nuclotron Accelerator in Laboratory of High Energies of Joint Institute for Nuclear Research in Dubna, Russia. Neutrons generated by the spallation reactions of 0.7, 1.0, 1.5 and 2 GeV protons and lead target interact with subcritical uranium blanket. In the neutron field outside the blanket, radioactive iodine, neptunium, plutonium and americium samples were irradiated and transmutation reaction yields (residual nuclei production yields) have been determined using -spectroscopy. Neutron field's energy distribution has also been studied using a set of threshold detectors. Results of transmutation studies of 129I, 237Np, 238Pu, 239Pu and 241Am are presented.

  11. Diffusivity of Sr, I and Pu in Granite With Through-Diffusion Experiment

    DEFF Research Database (Denmark)

    Dang, Hai-Jun; Hou, Xiaolin; Liu, Wen-yuan;

    2014-01-01

    The diffusion behavior of Sr, I and Pu in granite was investigated by through-diffusion experiment. the effective diffusion coefficients of Sr, I and Pu in granite at 26 °C were determined to be (1.24±0.03)×10-13 m2/s, (2.88±0.02)×10-13 m2/s and (1.33±0.52)×10-13 m2/s, respectively. It is also ob...

  12. Unconventional superconductivity in PuRhGa{sub 5}: Ga NMR/NQR study

    Energy Technology Data Exchange (ETDEWEB)

    Sakai, H. [Advanced Science Research Center, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan)]. E-mail: sakai.hironori@jaea.go.jp; Tokunaga, Y. [Advanced Science Research Center, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Fujimoto, T. [Advanced Science Research Center, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Kambe, S. [Advanced Science Research Center, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Walstedt, R.E. [Advanced Science Research Center, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Yasuoka, H. [Advanced Science Research Center, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Aoki, D. [Institute for Materials Research, Tohoku University, Oarai, Ibaraki 311-1313 (Japan); Homma, Y. [Institute for Materials Research, Tohoku University, Oarai, Ibaraki 311-1313 (Japan); Yamamoto, E. [Advanced Science Research Center, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Nakamura, A. [Advanced Science Research Center, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Shiokawa, Y. [Advanced Science Research Center, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Institute for Materials Research, Tohoku University, Oarai, Ibaraki 311-1313 (Japan); Nakajima, K. [Department of Nuclear Energy System, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Arai, Y. [Department of Nuclear Energy System, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Matsuda, T.D. [Advanced Science Research Center, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Haga, Y. [Advanced Science Research Center, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Onuki, Y. [Advanced Science Research Center, Japan Atomic Energy Research Institute, Tokai, Ibaraki 319-1195 (Japan); Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043 (Japan)

    2006-05-01

    {sup 69,71}Ga NMR/NQR studies have been performed on a single crystal of the transuranium superconductor PuRhGa{sub 5} with T{sub c}{approx}9K. The spin-lattice relaxation rate 1/T{sub 1} reveals that PuRhGa{sub 5} is an unconventional superconductor having an anisotropic superconducting gap. Moreover, Korringa behavior (1/T{sub 1}T=const.) is observed in the normal state below {approx}30K. This result suggests that the superconductivity sets in after the formation of a Fermi liquid state in this compound.

  13. Control of microstructural damage produced by helium in /sup 238/PuO/sub 2/ pellets

    Energy Technology Data Exchange (ETDEWEB)

    McDonell, W.R.; Gould, T.H. Jr.

    1978-01-01

    Interim heating above 1200/sup 0/C at intervals less than 6 months released helium without grain-boundary separations in small-grained, 80%-dense /sup 238/PuO/sub 2/ pellets stored for long times at low temperatures. However, preheating at temperatures below the 1200/sup 0/C threshold for grain separation did not release sufficient helium to prevent grain separations at higher temperatures. Size limits on the high-density regions of the microstructure will be necessary to avoid grain separations produced by helium release in /sup 238/PuO/sub 2/ after prolonged storage, if the interim release treatments cannot be conveniently employed.

  14. 137Cs and (239+240)Pu levels in the Asia-Pacific regional seas.

    Science.gov (United States)

    Duran, E B; Povinec, P P; Fowler, S W; Airey, P L; Hong, G H

    2004-01-01

    137Cs and (239+240)Pu data in seawater, sediment and biota from the regional seas of Asia-Pacific extending from 50 degrees N to 60 degrees S latitude and 60 degrees E to 180 degrees E longitude based on the Asia-Pacific Marine Radioactivity Database (ASPAMARD) are presented and discussed. 137Cs levels in surface seawater have been declining to its present median value of about 3 Bq/m3 due mainly to radioactive decay, transport processes, and the absence of new significant inputs. (239+240)Pu levels in surface seawater are much lower, with a median of about 6 mBq/m3. (239+240)Pu appears to be partly scavenged by particles and is therefore more readily transported down the water column. As with seawater, (239+240)Pu concentrations are lower than 137Cs in surface sediment. The median 137Cs concentration in surface sediment is 1.4 Bq/kg dry, while that of (239+240)Pu is only 0.2 Bq/kg dry. The vertical profiles of both 137Cs and (239+240)Pu in the sediment column of coastal areas are different from deep seas which can be attributed to the higher sedimentation rates and additional contribution of run-offs from terrestrial catchment areas in the coastal zone. Comparable data for biota are far less extensive than those for seawater and sediment. The median 137Cs concentration in fish (0.2 Bq/kg wet) is higher than in crustaceans (0.1 Bq/kg wet) or mollusks (0.1 Bq/kg wet). Benchmark values (as of 2001) for 137Cs and (239+240)Pu concentrations in seawater, sediment and biota are established to serve as reference values against which the impact of future anthropogenic inputs can be assessed. ASPAMARD represents one of the most comprehensive compilations of available data on 137Cs and (239+240)Pu in particular, and other anthropogenic as well as natural radionuclides in seawater, sediment and biota from the Asia-Pacific regional seas.

  15. Ideal Strengths and Bonding Properties of PuO2 under Tension

    Institute of Scientific and Technical Information of China (English)

    WANG Bao-Tian; MANG Ping

    2011-01-01

    We perform a first-principles computational tensile test on PuO2 based on density-functional theory within a local density approximation ( LDA )+U formalism to investigate its structural, mechanical, magnetic and intrinsic bonding properties in four representative directions: [001], [100], [110]and [111].The stress-strain relations show that the ideal tensile strengths in the four directions are 81.2, 80.5, 28.3 and 16.8GPa at strains of 0.36, 0.36,0.22 and 0.18, respectively.The [001]and [100]directions are prominently stronger than the other two directions since more Pu-O bonds participate in the pulling process.By charge and density of state analysis along the [001]direction, we find that the strong mixed ionic/covalent character of the Pu-O bond is weakened by tensile strain and PuO2 will exhibit an insulator-to-metal transition after tensile stresses exceeding about 79 GPa.%@@ We perform a first-principles computational tensile test on Pu02 based on density-functional theory within a local density approximation(LDA)+U formalism to investigate its structural, mechanical, magnetic and intrinsic bonding properties in four representative directions:[001], [100], [110] and [111].The stress-strain relations show that the ideal tensile strengths in the four directions are 81.2, 80.5, 28.3 and 16.8 GPa at strains of 0.36, 0.36,0.22 and 0.18, respectively.The [001]and [100]directions are prominently stronger than the other two directions since more Pu-0 bonds participate in the pulling process.By charge and density of state analysis along the[001]direction,we find that the strong mixed ioni%ovalent character of the Pu-0 bond is weakened by tensile strain and PuO2 will exhibit an insulator-to-metal transition after tensile stresses exceeding about 79 GPa.

  16. COMPLIANCE ANALYSIS, OPTIMISATION AND COMPARISON OF A NEW 3PUS-PU MECHANISM

    Directory of Open Access Journals (Sweden)

    B. Wei

    2013-06-01

    Full Text Available This paper investigates the compliance of a new 3PUS-PU hybrid mechanism with three degrees of freedom, including translation along the Z axis and rotations about the X and Y axes. Firstly, the kinematic analysis of the mechanism is analysed and the compliance model of the mechanism derived. Secondly, the effects the geometric parameters and position and orientation parameters on the compliance of the mechanism in each direction are investigated, and the genetic algorithm is used to optimise the global compliance by simultaneously adjusting design variables. Finally, the compliance of two similar kinds of 3PUS-PU mechanism in each direction is reviewed.

  17. PIXE analysis of U and Pu from hot particles: K-lines vs L-lines

    DEFF Research Database (Denmark)

    Jiménez-Ramos, M.C.; García López, J.; Eriksson, M.;

    2012-01-01

    . (2007) [1] and Jiménez-Ramos et al. (2010) [2], radioactive particles from aircraft accidents in Palomares and Thule have been characterized. Using micro-Proton Induced X-ray Emission (μ-PIXE) and confocal X-ray fluorescence microprobe (μ-XRF), the L-lines of the main components in these particles, U...... and Pu, were analyzed.In this work, the key goal is the possibility to determine elemental ratios and concentration of transuranic elements in hot particles from the same areas but using their K-lines, because of their advantages in comparison with the study of L-lines. Indeed, the U and Pu K...

  18. Monitoring intakes of Pu/Am by external counting. Current status in India

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, R.C.; Surendran, T.; Haridasan, T.K. [Internal Dosimetry Division, Bhabha Atomic Reserch Centre, Mumbai (India)

    2000-05-01

    This paper describes the current status of the direct methods of monitoring intakes of actinides, Pu/Am, by external counting techniques in India. It begins with the brief descriptions of the in vivo monitoring facilities established and a variety of optimised radiation detectors being operated inside the graded lined steel room chamber. Two types of phoswich detectors (200 mm dia) differing in the thicknesses of their primary detectors, are operated with pulse shape discrimination electronics based on pulse shape analyser (ORTEC model 458). The other detection systems are : 51 mm dia coaxial HPGe low energy photon spectrometer, a miniature CdTe and a twin thin NaI(Tl). Over the past several years, these facilities have been rationally utilized for conducting various types of internal monitoring programmes for workers handing Pu/Am. Due emphasis has been given to the Quality Assurance (QA) programmes and thus the accuracy of internal exposure evaluations has been ensured by participating in the international intercomparison studies. These included: a) In vivo calibration experiments based on inhalation of mock Pu i.e. polystyrene particles labelled with {sup 103}Pd - {sup 51}Cr, by human volunteers; b) Calibration measurements on Lawrence Livermore National Laboratory's (LLNL) realistic thorax phantom representing a Caucasian man, under an IAEA-CRP and c) By participating in yet another IAEA-CRP on the calibration of in vivo counting systems for actinides (Pu, Am, U, Th) using a Reference Asian phantom whose physique represented an Asian man of Japanese origin. As both, ICRP and BSS of IAEA recommend the use of latest dose coefficients, the current methodology of evaluating internal exposures to actinides (Pu/Am) is based on the new (ICRP-66) model of the human respiratory tract. For this purpose, the software package LUDEP 2.05 (Lung Dose Evaluation Program) has been standardised for routine use. The use of LUDEP 2.05 for calculating intakes and committed

  19. On Pu-244 in lunar rocks from Fra Mauro and implications regarding their origin.

    Science.gov (United States)

    Marti, K.; Lightner, B. D.; Lugmair, G. W.

    1973-01-01

    The evidence for in situ produced fission xenon from Pu-244 in rock 14321 is presented. The inferred abundance ratio Pu-244/U-238 is found to be consistent with values observed in a meteorite. Data from a stepwise release of the xenon permits a characterization of the trapped component, which can be shown to be distinct from solar xenon. We discuss the evidence for the presence of fission gases and of uncorrelated radiogenic argon in this and in other Apollo 14 rocks and some implications regarding their origin.

  20. Clean Air Markets - Allowances Query Wizard

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Allowances Query Wizard is part of a suite of Clean Air Markets-related tools that are accessible at http://camddataandmaps.epa.gov/gdm/index.cfm. The Allowances...

  1. Allowance Holdings and Transfers Data Inventory

    Data.gov (United States)

    U.S. Environmental Protection Agency — The Allowance Holdings and Transfers Data Inventory contains measured data on holdings and transactions of allowances under the NOx Budget Trading Program (NBP), a...

  2. El puñal bidiscoidal peninsular: tipología y relación con el puñal militar romano (pugio

    Directory of Open Access Journals (Sweden)

    Kavanagh de Prado, Eduardo

    2008-12-01

    Full Text Available The hypothesis that considered the Celtiberian Iron Age «bidiscoidal» type dagger (also traditionally known as «doubleglobular» or «biglobular» as the prototype of the pugio, or dagger used by the Roman legionaires since the Late Republic, was put forward by specialists as early as the begining of the 20th century. The main purpose of this paper is to provide an analysis of the «bidiscoidal» dagger and of its evolution. Our second objective, derived from the first, is to prove the filiation of the Roman legionary dagger (pugio as an evolution of the Celtiberian prototype.

    La historiografía de principios del s. XX recogía ya la teoría que relacionaba el puñal «bidiscoidal» (tradicionalmente denominado «dobleglobular» o «biglobular» característico de la cultura celtibérica del Hierro II, con el pugio, puñal usado por los legionarios romanos al menos desde el fin de la República. La razón estriba en la evidente similitud tipológica, en concepción general y detalles, entre ambos tipos. El objetivo principal de este trabajo es presentar un análisis del puñal bidiscoidal y su evolución a caballo entre ambos universos, celtibérico y romano. Secundariamente, demostrar la filiación entre ambas armas: el origen celtibérico del puñal romano legionario (pugio.

  3. 46 CFR 154.428 - Allowable stress.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Allowable stress. 154.428 Section 154.428 Shipping COAST GUARD, DEPARTMENT OF HOMELAND SECURITY (CONTINUED) CERTAIN BULK DANGEROUS CARGOES SAFETY STANDARDS FOR... § 154.428 Allowable stress. The membrane tank and the supporting insulation must have allowable stresses...

  4. 46 CFR 154.447 - Allowable stress.

    Science.gov (United States)

    2010-10-01

    ... 46 Shipping 5 2010-10-01 2010-10-01 false Allowable stress. 154.447 Section 154.447 Shipping COAST... Tank Type B § 154.447 Allowable stress. (a) An independent tank type B designed from bodies of revolution must have allowable stresses 3 determined by the following formulae: 3 See Appendix B for stress...

  5. Sustained PU.1 levels balance cell-cycle regulators to prevent exhaustion of adult hematopoietic stem cells.

    Science.gov (United States)

    Staber, Philipp B; Zhang, Pu; Ye, Min; Welner, Robert S; Nombela-Arrieta, César; Bach, Christian; Kerenyi, Marc; Bartholdy, Boris A; Zhang, Hong; Alberich-Jordà, Meritxell; Lee, Sanghoon; Yang, Henry; Ng, Felicia; Zhang, Junyan; Leddin, Mathias; Silberstein, Leslie E; Hoefler, Gerald; Orkin, Stuart H; Göttgens, Berthold; Rosenbauer, Frank; Huang, Gang; Tenen, Daniel G

    2013-03-07

    To provide a lifelong supply of blood cells, hematopoietic stem cells (HSCs) need to carefully balance both self-renewing cell divisions and quiescence. Although several regulators that control this mechanism have been identified, we demonstrate that the transcription factor PU.1 acts upstream of these regulators. So far, attempts to uncover PU.1's role in HSC biology have failed because of the technical limitations of complete loss-of-function models. With the use of hypomorphic mice with decreased PU.1 levels specifically in phenotypic HSCs, we found reduced HSC long-term repopulation potential that could be rescued completely by restoring PU.1 levels. PU.1 prevented excessive HSC division and exhaustion by controlling the transcription of multiple cell-cycle regulators. Levels of PU.1 were sustained through autoregulatory PU.1 binding to an upstream enhancer that formed an active looped chromosome architecture in HSCs. These results establish that PU.1 mediates chromosome looping and functions as a master regulator of HSC proliferation.

  6. Distribution and source of 129I, 239,240Pu, 137Cs in the environment of Lithuania

    DEFF Research Database (Denmark)

    Ezerinskis, Z.; Hou, Xiaolin; Druteikiene, R.;

    2016-01-01

    Fifty five soil samples collected in the Lithuania teritory in 2011 and 2012 were analyzed for 129I, 137Cs and Pu isotopes in order to investigate the level and distribution of artificial radioactivity in Lithuania. The activity and atomic ratio of 238Pu/239,240Pu, 129I/127I and 131I/137Cs were...... used to identify the origin of these radionuclides. The 238Pu/239þ240Pu and 240Pu/239Pu ratios in the soil samples analyzed varied in the range of 0.02e0.18 and 0.18e0.24, respectively, suggesting the global fallout as the major source of Pu in Lithuania. The values of 109 to 106 for 129I/127I atomic...... ratio revealed that the source of 129I in Lithuania is global fallout in most cases though several sampling sites shows a possible impact of reprocessing releases. Estimated 129I/131I ratio in soil samples from the southern part of Lithuania shows negligible input of the Chernobyl fallout...

  7. Determination and comparison of γ-aminobutyric acid (GABA) content in pu-erh and other types of Chinese tea.

    Science.gov (United States)

    Zhao, Ming; Ma, Yan; Wei, Zhen-zhen; Yuan, Wen-xia; Li, Ya-li; Zhang, Chun-hua; Xue, Xiao-ting; Zhou, Hong-jie

    2011-04-27

    Two previous studies have reported that pu-erh tea contains a high level of γ-aminobutyric acid (GABA), which is the major inhibitory neurotransmitter in the central nervous system and has several physiological functions. However, two other researchers have demonstrated that the GABA content of several pu-erh teas was low. Due to the high value and health benefits of GABA, analysis of mass-produced pu-erh tea is necessary to determine whether it is actually enriched with GABA. A high-performance liquid chromatography (HPLC) method was developed for the determination of GABA in tea, the results of which were verified by amino acid analysis using an Amino Acid Analyzer (AAA). A total of 114 samples of various types of Chinese tea, including 62 pu-erh teas, 13 green teas, 8 oolong teas, 8 black teas, 3 white teas, 4 GABA teas, and 16 process samples from two industrial fermentations of pu-erh tea (including the raw material and the first to seventh turnings), were analyzed using HPLC. Statistical analysis demonstrated that the GABA content in pu-erh tea was significantly lower than that in other types of tea (p content decreased during industrial fermentation of pu-erh tea (p content in pu-erh tea. In addition, the GABA content in white tea was found to be significantly higher than that in the other types of tea (p < 0.05), leading to the possibility of producing GABA-enriched white tea.

  8. Cumulative deposition of fallout-derived {sup 137}Cs, {sup 90}Sr, {sup 239,240}Pu in environmental samples

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Myung Ho; Choi, Gun Sik; Hong, Kwang Hee; Cho, Yung Hyun; Lee, Chang Woo [KAERI, Taejon (Korea, Republic of)

    1999-07-01

    The data of cumulative depositions of {sup 239,240}Pu, {sup 90}Sr and {sup 137}Cs in the terrestrial soil and sea sediment of Korea are presented in this paper. The highest inventory of {sup 239,240}Pu, {sup 90}Sr and {sup 137}Cs was found in the volcanic ash soil and the lowest inventory was found in the arable soil. Organic substances and rainfall have a significant influence on deposition of {sup 239,240}Pu, {sup 90}Sr and {sup 137}Cs in the terrestrial soil. From depth profiles, most of {sup 239,240}Pu, {sup 90}Sr and {sup 137}Cs is accumulated in the layer of upper 10 cm of soil and the concentrations of {sup 239,240}Pu, {sup 90}Sr and {sup 137}Cs decreased with increasing depth. The maximum concentrations of {sup 239,240}Pu and {sup 137}Cs in the sediment match the input records of global fallout. The activity ratios of {sup 239,240}Pu / {sup 137}Cs and {sup 90}Sr / {sup 137}Cs in the terrestrial soil are close to the estimated value attributed to the fallout. The activity ratios of {sup 239,240}Pu / {sup 137}Cs in the sediment were higher than those in terrestrial soils. (author). 18 refs., 1 tab., 5 figs.

  9. Hemodynamics and the parameters of the heart mass in the dog after inhalation of submicron /sup 239/Pu dioxide

    Energy Technology Data Exchange (ETDEWEB)

    Kalmykova, Z.I.; Buldakov, Z.I.; Kharunzhin, V.V.

    The growth of the right heart mass was mainly registered in dogs after inhalation of different quantities of /sup 239/Pu submicron dioxide. This was correlated with the value of /sup 239/Pu deposited in the lungs and associated with the systemic hemodynamic disorders.

  10. PU-H71 effectively induces degradation of IκB kinase β in the presence of TNF-α.

    Science.gov (United States)

    Qu, Zhuling; Wang, Shiduan; Teng, Ruyang; Yi, Xuanlong

    2014-01-01

    This study is to determine if PU-H71, a heat shock protein inhibitor, induces killing of malignant breast cells together with treatment of tumor necrosis factor-α (TNF-α). The related molecular mechanisms were also studied. A primary mammary epithelial cell line HMEC2595 cells and the highly metastatic breast cell line MDA-MB-231, the HER2-positive BT-474 cells, and the ER-positive MCF7 cells were treated with PU-H71 in the presence or absence of TNF-α. The effects of PU-H71 and TNF-α treatments on cells viabilities and on intracellular signaling pathway proteins were determined using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay, apoptosis assays, immunoblot assays, and luciferase assays. It was found that TNF-α enhances the toxic effects of PU-H71 on tumor cells but not normal cells. PU-H71 treatments lead to degradation of IKKβ. Moreover, PU-H71 down-regulates the NF-κB transcriptional activity induced by TNF-α treatment. The experimental results indicated PU-H71 effectively induces cell killing of malignant breast cells in the presence of TNF-α, possibly through a mechanism related to degradation of IKKβ. It is suggested that combination of PU-H71 and TNF-α treatments might be an effective therapeutic strategy of breast malignancies.

  11. High temperature phase transition of mixed (PuO2 + ThO2) investigated by laser melting

    NARCIS (Netherlands)

    Böhler, R.; Cakir, P.; Benes, O.; Hein, H.; Konings, R.J.M.; Manara, D.

    2014-01-01

    A laser heating approach combined with fast pyrometry in a thermal arrest method was used to provide new data for the melting/solidification phase transition in mixed (PuO2 + ThO2) at high temperature. At low concentration of ThO2 in PuO2 a minimum in the solidification temperature in the pseudo bin

  12. CP actuator based on chemically-deposited polypyrrole and PU based solid polymer electrolyte working in air

    Science.gov (United States)

    Choi, Hwa Jeong; Lim, Hyun-Ok; Chung, Ildoo; Ryu, Kwang-Sun; Jo, Nam-Ju

    2007-07-01

    Conducting polymers (CPs), such as polypyrrole, polythiophene and polyaniline, are unique in that they have switchable properties due to their two or more mechanically stable oxidation state. Thus, their films or coatings can be easily switched by the application of small voltage and current to change volume during their electrochemical redox process. In particular, polypyrrole (PPy) has been studied most extensively because of its high electrical conductivity and good environmental stability under ambient condition. In this work, we have studied a new CP actuator, fully polymeric, assembled with two PPy film electrodes and a solid polymer electrolyte (SPE), polyurethane/Mg(ClO 4) II. Polyurethanes (PUs) were synthesized from 4,4'-diphenylmethane diisocyanate (MDI), 1,4-butanediol (1,4-BD) and three types of polyols, poly(ethylene glycol) (PEG), poly(propylene glycol) (PPG), and PPG-block-PEG-block-PPG (PPG-co-PEG). The chemical polymerization of PPy by immersion in Py monomer aqueous solution and oxidant aqueous solution is an adequate method to prepare PU/PPy composite film as actuator. To find the proper thickness of PPy coating layer for actuation, we measured the displacement of actuators according to the thickness of PPy coating layer. And, the displacement of all actuators was discussed in connection with the properties of SPE and PPy. All the results obtained in this work show the feasibility of electrochemomechanical devices based on PPy and SPE film able to work in air.

  13. Alpha and conversion electron spectroscopy of {sup 238,239}Pu and {sup 241}Am and alpha-conversion electron coincidence measurements

    Energy Technology Data Exchange (ETDEWEB)

    Dion, Michael P., E-mail: michael.dion@pnnl.gov; Miller, Brian W.; Warren, Glen A.

    2016-09-11

    A technique to determine the isotopic constituents of a mixed actinide sample has been proposed by a coincident alpha-conversion electron measurement. This presents a unique signature to allow the unfolding of isotopes that possess overlapping alpha particle energy and reduce backgrounds of an unseparated sample. The work presented here are results of conversion electron spectroscopy of {sup 241}Am, {sup 238}Pu and {sup 239}Pu using a dual-stage peltier-cooled 25 mm{sup 2} silicon drift detector and alpha spectroscopy with a passivated ion implanted planar silicon detector. The conversion electron spectra were evaluated from 20–55 keV based on fits to the dominant conversion electron emissions, which allowed the relative conversion electron emission intensities to be determined. These measurements provide crucial singles spectral information and calibration to aid in the coincident measurement approach. Furthermore, an alpha-conversion electron spectrometer was assembled using the silicon based detectors described and results of a coincident spectrum analysis is reported for {sup 241}Am.

  14. Co-extraction and co-stripping of U(VI) and Pu(IV) using tri-iso-amyl phosphate and tri-n-butyl phosphate in n-dodecane from nitric acid media under high loading conditions

    Energy Technology Data Exchange (ETDEWEB)

    Sreenivasulu, Balija; Suresh, Ammath; Sivaraman, Nagarajan; Rao, P.R. Vasudeva [Indira Gandhi Centre for Atomic Research, Kalpakkam (India). Chemistry Group

    2016-08-01

    The extraction of Pu(IV) using 1.1 M solution of tri-iso-amyl phosphate (TiAP)/n-dodecane (DD) from plutonium nitrate solutions in nitric acid media was examined as a function of equilibrium aqueous phase metal ion concentration and equilibrium aqueous phase acidity at 303 K. The nitric acid concentration in the organic phase was measured as a function of equilibrium organic phase plutonium concentration. The co-extraction of U(VI) and Pu(IV) was studied using 1.1 M TiAP/DD system as a function of their equilibrium aqueous phase metal ion concentration and compared with 1.1 M tri-n-butyl phosphate (TBP)/n-DD system under identical conditions. Co-extraction and co-stripping of U(VI) and Pu(IV) were studied using 1.1 M TiAP/DD and 1.1 M TBP/DD systems in cross current mode to evaluate the number of stages required for the extraction and stripping of heavy metal ions (uranium and plutonium). The extraction and stripping efficiencies were calculated for both the systems. The saturation limit of the organic phase was also established in these studies.

  15. Aluminum Target Dissolution in Support of the Pu-238 Program

    Energy Technology Data Exchange (ETDEWEB)

    McFarlane, Joanna [ORNL; Benker, Dennis [ORNL; DePaoli, David W [ORNL; Felker, Leslie Kevin [ORNL; Mattus, Catherine H [ORNL

    2014-09-01

    Selection of an aluminum alloy for target cladding affects post-irradiation target dissolution and separations. Recent tests with aluminum alloy 6061 yielded greater than expected precipitation in the caustic dissolution step, forming up to 10 wt.% solids of aluminum hydroxides and aluminosilicates. We present a study to maximize dissolution of aluminum metal alloy, along with silicon, magnesium, and copper impurities, through control of temperature, the rate of reagent addition, and incubation time. Aluminum phase transformations have been identified as a function of time and temperature, using X-ray diffraction. Solutions have been analyzed using wet chemical methods and X-ray fluorescence. These data have been compared with published calculations of aluminum phase diagrams. Temperature logging during the transients has been investigated as a means to generate kinetic and mass transport data on the dissolution process. Approaches are given to enhance the dissolution of aluminum and aluminosilicate phases in caustic solution.

  16. Melting behavior of mixed U-Pu oxides under oxidizing conditions

    Science.gov (United States)

    Strach, Michal; Manara, Dario; Belin, Renaud C.; Rogez, Jacques

    2016-05-01

    In order to use mixed U-Pu oxide ceramics in present and future nuclear reactors, their physical and chemical properties need to be well determined. The behavior of stoichiometric (U,Pu)O2 compounds is relatively well understood, but the effects of oxygen stoichiometry on the fuel performance and stability are often still obscure. In the present work, a series of laser melting experiments were carried out to determine the impact of an oxidizing atmosphere, and in consequence the departure from a stoichiometric composition on the melting behavior of six mixed uranium plutonium oxides with Pu content ranging from 14 to 62 wt%. The starting materials were disks cut from sintered stoichiometric pellets. For each composition we have performed two laser melting experiments in pressurized air, each consisting of four shots of different duration and intensity. During the experiments we recorded the temperature at the surface of the sample with a pyrometer. Phase transitions were qualitatively identified with the help of a reflected blue laser. The observed phase transitions occur at a systematically lower temperature, the lower the Pu content of the studied sample. It is consistent with the fact that uranium dioxide is easily oxidized at elevated temperatures, forming chemical species rich in oxygen, which melt at a lower temperature and are more volatile. To our knowledge this campaign is a first attempt to quantitatively determine the effect of O/M on the melting temperature of MOX.

  17. Melting behavior of mixed U–Pu oxides under oxidizing conditions

    Energy Technology Data Exchange (ETDEWEB)

    Strach, Michal [CEA, DEN, DTEC, SECA, LCC, Cadarache F-13108, Saint-Paul-Lez-Durance (France); IM2NP, UMR CNRS 7334 – Aix Marseille University, Case 251, Avenue Escadrille Normandie Niemen, 13397 Marseille Cedex 20 (France); Manara, Dario [European Commission, Joint Research Centre, Institute for Transuranium Elements, P.O. Box 2340, 76125 Karlsruhe (Germany); Belin, Renaud C. [CEA, DEN, DTEC, SECA, LCC, Cadarache F-13108, Saint-Paul-Lez-Durance (France); Rogez, Jacques [IM2NP, UMR CNRS 7334 – Aix Marseille University, Case 251, Avenue Escadrille Normandie Niemen, 13397 Marseille Cedex 20 (France)

    2016-05-01

    In order to use mixed U–Pu oxide ceramics in present and future nuclear reactors, their physical and chemical properties need to be well determined. The behavior of stoichiometric (U,Pu)O{sub 2} compounds is relatively well understood, but the effects of oxygen stoichiometry on the fuel performance and stability are often still obscure. In the present work, a series of laser melting experiments were carried out to determine the impact of an oxidizing atmosphere, and in consequence the departure from a stoichiometric composition on the melting behavior of six mixed uranium plutonium oxides with Pu content ranging from 14 to 62 wt%. The starting materials were disks cut from sintered stoichiometric pellets. For each composition we have performed two laser melting experiments in pressurized air, each consisting of four shots of different duration and intensity. During the experiments we recorded the temperature at the surface of the sample with a pyrometer. Phase transitions were qualitatively identified with the help of a reflected blue laser. The observed phase transitions occur at a systematically lower temperature, the lower the Pu content of the studied sample. It is consistent with the fact that uranium dioxide is easily oxidized at elevated temperatures, forming chemical species rich in oxygen, which melt at a lower temperature and are more volatile. To our knowledge this campaign is a first attempt to quantitatively determine the effect of O/M on the melting temperature of MOX.

  18. Exploiting Channel Correlation and PU Traffic Memory for Opportunistic Spectrum Scheduling

    CERN Document Server

    Wang, Shanshan; Zhang, Junshan

    2012-01-01

    We consider a cognitive radio network with multiple primary users (PUs) and one secondary user (SU), where a spectrum server is utilized for spectrum sensing and scheduling the SU to transmit over one of the PU channels opportunistically. One practical yet challenging scenario is when \\textit{both} the PU occupancy and the channel fading vary over time and exhibit temporal correlations. Little work has been done for exploiting such temporal memory in the channel fading and the PU occupancy simultaneously for opportunistic spectrum scheduling. A main goal of this work is to understand the intricate tradeoffs resulting from the interactions of the two sets of system states - the channel fading and the PU occupancy, by casting the problem as a partially observable Markov decision process. We first show that a simple greedy policy is optimal in some special cases. To build a clear understanding of the tradeoffs, we then introduce a full-observation genie-aided system, where the spectrum server collects channel fa...

  19. PuMa-II: A wide band pulsar machine for the Westerbork Synthesis Radio Telescope

    NARCIS (Netherlands)

    Karuppusamy, R.; Stappers, B.; van Straten, W.

    2008-01-01

    The Pulsar Machine II (PuMa-II) is the new flexible pulsar processing back-end system at the Westerbork Synthesis Radio Telescope (WSRT), specifically designed to take advantage of the upgraded WSRT. The instrument is based on a computer cluster running the Linux operating system, with minimal custo

  20. A Density Functional Study of Atomic Carbon Adsorption on δ-Pu(111)Surface

    Institute of Scientific and Technical Information of China (English)

    WEI Hong-Yuan; XIONG Xiao-Ling; SONG Hong-Tao; LUO Shun-Zhong

    2010-01-01

    @@ Adsorption of atomic carbon on δ-Pu(111)surface is investigated systematically using density functional theory with RPBE functional.The adsorption energies,adsorption structures,Mulliken population,work functions,layer and projected density of states are calculated in wide ranges of coverage,which have never been studied before as far as we know.

  1. A Discussion of Reversible and Irreversible Sorption for Sr, Cs, Np, and Pu

    Energy Technology Data Exchange (ETDEWEB)

    Carroll, Susan [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Tinnacher, Ruth [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Kersting, Annie [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Zavarin, Mavrik [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2010-04-30

    Here we discuss the possibility that fission product and actinide sorption is reversible when thermodynamic and kinetic factors are accounted for in predictive models. We do this by reviewing the sorption behavior of Sr, Cs, Np, and Pu, and by reviewing our ability to model their sorption behavior.

  2. Solid Phase Extraction Disk Procedure to Determine 239Pu in Soils

    Directory of Open Access Journals (Sweden)

    ZHANG Ji-qiao;ZHAO Ya-ping;DING You-qian;ZHANG Sheng-dong;YANG Jin-ling

    2016-11-01

    Full Text Available 239Pu in many soil samples should be analyzed to survey radioactive pollution level in nuclear facilities and its affinity environment efficiently. In order to input the opt conditions for column experiment, the experiments of the static adsorption coefficient of 239Pu to solid phase extraction disk with different contact time, concentration of HNO3 and different temperature were carried out. The chemical procedure for the rapid separation and determination of 239Pu in soils had been formulated, which using solid phase extraction disk (EmporeTM Anion Exchange-SR as extraction material and liquid scintillation spectrometry counting as measurement. In the procedure, soil sample usage was 10 g, and were leached by 8 mol/L HNO3, the chemical recovery of the procedure was about 78.9%, and the minimum detectable concentration was 3.7 Bq/kg. It took less than 3 hours once and the presence of 137Cs, 90Sr-90Y and natural uranium, 241Am, 99Tc did not interfere with the procedure, owning high DF of them. The procedure can be used extensively in determination of 239Pu in soils.

  3. Yield-Energy Evaluation of 85Kr of 239Pu+n Fission

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    <正>The yields of 85Kr, the important production of the 239Pu fission, were re-evaluated over the incident neutron energy 1-15 MeV, based upon all the experimental data. The yields as function of energ

  4. /sup 238/Pu fuel form processes quarterly report, April-June 1980

    Energy Technology Data Exchange (ETDEWEB)

    Folger, R. L.

    1980-06-01

    Savannah River Laboratory (SRL) completed the development of a production process to fabricate /sup 238/PuO/sub 2/ fuel forms for the GPHS. The fabrication flowsheet was based on a flowsheet originally developed at Los Alamos National Scientific Laboratory (LANSL). A summary report of the SRL process development effort is presented.

  5. Estimates for Pu-239 loadings in burial ground culverts based on fast/slow neutron measurements

    Energy Technology Data Exchange (ETDEWEB)

    Winn, W.G.; Hochel, R.C.; Hofstetter, K.J.; Sigg, R.A.

    1989-08-15

    This report provides guideline estimates for Pu-239 mass loadings in selected burial ground culverts. The relatively high recorded Pu-239 contents of these culverts have been appraised as suspect relative to criticality concerns, because they were assayed only with the solid waste monitor (SWM) per gamma-ray counting. After 1985, subsequent waste was also assayed with the neutron coincidence counter (NCC), and a comparison of the assay methods showed that the NCC generally yielded higher assays than the SWM. These higher NCC readings signaled a need to conduct non-destructive/non-intrusive nuclear interrogations of these culverts, and a technical team conducted scoping measurements to illustrate potential assay methods based on neutron and/or gamma counting. A fast/slow neutron method has been developed to estimate the Pu-239 in the culverts. In addition, loading records include the SWM assays of all Pu-239 cuts of some of the culvert drums and these data are useful in estimating the corresponding NCC drum assays from NCC vs SWM data. Together, these methods yield predictions based on direct measurements and statistical inference.

  6. Reliable determination of 237Np in environmental solid samples using 242Pu as a potential tracer

    DEFF Research Database (Denmark)

    Qiao, Jixin; Hou, Xiaolin; Roos, Per;

    2011-01-01

    onto various AG 1-type anion exchangers; suitability of 242Pu as a tracer for 237Np determination in environmental solid samples; and long-term chemical stability of tetravalent Np. Experimental results revealed that the degree of resin cross-linking has a significant influence on the separation...

  7. Characterization of Hydrogen Interactions with δ-Pu using Electronic Structure Theory

    Science.gov (United States)

    Taylor, Christopher D.; Hernandez, Sarah C.

    2012-02-01

    The generalized gradient approximation to density functional theory was used to study surface, bulk, defect, and reaction states of hydrogen in δ-Pu. The quasi-disordered anti-ferromagnetic arrangement gave a volume of 24.1 å^3 and a bulk modulus of 48.1 GPa for δ-Pu, in reasonable agreement with the experimental values of 24.9 å^3 and 30-35 GPa. This arrangement was thus subsequently used for all calculations. We have determined that hydrogen interactions with δ-Pu are exothermic in character at all levels ranging from dissociative chemisorption to interstitial absorption, the formation of hydrogen-vacancy complexes, and generation of a hydride phase. The exothermic character of these interactions appears to be the reason for the rapid hydriding reaction, which has been determined experimentally to be essentially a barrierless process. The anionic character is observed to be retained. Our studies also indicate that vacancies do not appear to be strong traps for hydrogen, since the interstitial absorption sites are exothermic in nature. We will propose a scheme by which hydrogen interacts with Pu. Results will be compared with previous studies in the literature where available.

  8. /sup 238/Pu fuel form processes. Quarterly report, July-September 1981

    Energy Technology Data Exchange (ETDEWEB)

    1982-04-01

    This report is one of a series to summarize progress in the Savannah River Laboratory /sup 238/Pu Fuel Form Program. Goals of the Savannah River Laboratory (SRL) program include providing technical support for the production of /sup 238/PuO/sub 2/ fuel forms in the Savannah River Plant's (SRP) Plutonium Fuel Form (PuFF) Facility. This part of the program includes: demonstration of processes and techniques developed by the Los Alamos National Laboratory (LANL) for production at SRP. Information from the demonstration will provide the technical data for technical standards and operating procedures; technical support to assist plant startup and to ensure continuation of safe and efficient production of high-quality heat-source fuel; and technical assistance after startup to accommodate changes in product and product specifications, to assist user agencies in improving product performance, to assist SRP in making process improvements that increase efficiency and product reliability, and to adapt plant facilities for new products. This report summarizes progress in improving the quality of welds in /sup 238/PuO/sub 2/ fuel capsules.

  9. Nucleogenic {sup 36}Cl, {sup 236}U and {sup 239}Pu in uranium ores

    Energy Technology Data Exchange (ETDEWEB)

    Wilcken, K.M. [Department of Nuclear Physics, RSPhysSE, Australian National University, Canberra, ACT 0200 (Australia); Scottish Universities Environmental Research Centre, Scottish Enterprise Technology Park, Rankine Avenue, East Kilbride G75 0QF (United Kingdom)], E-mail: K.Wilcken@suerc.gla.ac.uk; Fifield, L.K.; Barrows, T.T.; Tims, S.G.; Gladkis, L.G. [Department of Nuclear Physics, RSPhysSE, Australian National University, Canberra, ACT 0200 (Australia)

    2008-08-15

    The nucleogenic isotopes {sup 36}Cl, {sup 236}U and {sup 239}Pu are produced naturally in subsurface environments via neutron capture of thermal and epithermal neutrons. Concentrations are, however, very low and accelerator mass spectrometry (AMS) is required for quantitative measurements. A particular challenge is presented by the measurement of {sup 236}U/{sup 238}U ratios down to the level of 10{sup -13} that is expected from rocks with low uranium concentration. Here, we present the AMS methodology that has been developed at the ANU for measuring {sup 236}U/{sup 238}U ratios at this level. The more established methodologies for {sup 36}Cl and {sup 239}Pu measurements are also summarised. These capabilities are then used to characterize the {sup 36}Cl, {sup 236}U and {sup 239}Pu concentrations in a range of uranium ores. A simple model of the neutron production and capture processes in subsurface environments has been developed and is presented. It is shown that nucleogenic {sup 36}Cl, {sup 236}U and {sup 239}Pu can be used to determine both thermal and epithermal neutron fluxes in subsurface environments. Potential applications include uranium exploration and monitoring of the environmental impact of uranium mining.

  10. Nucleogenic 36Cl, 236U and 239Pu in uranium ores

    Science.gov (United States)

    Wilcken, K. M.; Fifield, L. K.; Barrows, T. T.; Tims, S. G.; Gladkis, L. G.

    2008-08-01

    The nucleogenic isotopes 36Cl, 236U and 239Pu are produced naturally in subsurface environments via neutron capture of thermal and epithermal neutrons. Concentrations are, however, very low and accelerator mass spectrometry (AMS) is required for quantitative measurements. A particular challenge is presented by the measurement of 236U/ 238U ratios down to the level of 10 -13 that is expected from rocks with low uranium concentration. Here, we present the AMS methodology that has been developed at the ANU for measuring 236U/ 238U ratios at this level. The more established methodologies for 36Cl and 239Pu measurements are also summarised. These capabilities are then used to characterize the 36Cl, 236U and 239Pu concentrations in a range of uranium ores. A simple model of the neutron production and capture processes in subsurface environments has been developed and is presented. It is shown that nucleogenic 36Cl, 236U and 239Pu can be used to determine both thermal and epithermal neutron fluxes in subsurface environments. Potential applications include uranium exploration and monitoring of the environmental impact of uranium mining.

  11. Influence of thermal and resonance neutron on fast neutron flux measurement by Pu-239 fission chamber

    CERN Document Server

    zeng, Lina; Song, Lingli; Zheng, Chun

    2014-01-01

    The Pu-239 fission chambers are widely used to measure fission spectrum neutron flux due to a flat response to fast neutrons. However, in the mean time the resonance and thermal neutrons can cause a significant influence on the measurement if they are moderated, which could be eliminated by using B and Cd covers. At a column enriched uranium fast neutron critical assembly, the fission reaction rates of Pu-239 are measured as 1.791*10-16,2.350*10-16 and 1.385*10-15 per second for 15mm thick B cover, 0.5mm thick Cd cover, and no cover respectively. While the fission reaction rate of Pu-239 is rapidly increased to 2.569*10-14 for a 20mm thick polythene covering fission chamber. The average Pu-239 fission cross-section of thermal and resonance neutrons is calculated to be 500b and 24.95b with the assumption of 1/v and 1/E spectra respectively, then thermal, resonance and fast neutron flux are achieved to be 2.30*106,2.24*106 and 1.04*108cm-2s-1.

  12. Measurement of absorption with a p-u sound intensity probe in an impedance tube

    DEFF Research Database (Denmark)

    Liu, Yang; Jacobsen, Finn

    2005-01-01

    An alternative method of measuring the normal-incidence sound absorption of a sample of material in an impedance tube is examined. The method is based on measurement of the sound pressure and the normal component of the particle velocity using a "p-u" sound intensity probe. This technique...

  13. New concept of designing Pu and MA containing fuel for fast reactors

    Science.gov (United States)

    Savchenko, A. M.; Konovalov, I. I.; Vatulin, A. V.; Glagovsky, E. M.

    2009-03-01

    New type of metal base fuel element is suggested for fast reactors. Basic approach to fuel element development - separated operations of fabricating uranium meat fuel element and introducing into it Pu or MA dioxides powder, that results in minimizing dust forming operations in fuel element fabrication. According to new fuel element design a framework fuel element having a porous uranium alloy meat is filled with standard PuO 2 powder of fuel meat metallurgically bonded to cladding forms a heat conducting framework, pores of which contain PuO 2 powder. Framework fuel element having porous meat is fabricated by capillary impregnation method with the use of Zr eutectic matrix alloys, which provides metallurgical bond between fuel and cladding and protects it from interaction. As compared to MOX fuel the new one features high thermal conductivity, higher uranium content, hence, high conversion ratio does not interact with fuel cladding and is more environmentally clean. Its principle advantage is a simple production process that is easily realized remotely, feasibility of involving high background Pu and MA isotopes into closed nuclear fuel cycle at the minimal influence on environment.

  14. Pre-separation of U, Np, Pu in 1AW Samplefor XRF Analysis

    Institute of Scientific and Technical Information of China (English)

    DENG; Wei-qin; TAN; Shu-ping; TAO; Miao-miao; WU; Ji-zong

    2013-01-01

    1AW is the liquid waste of the first separation unit of Purex process.The analysis of U,Np,Pu in1AW contributes to some key points,such as,the recovery of plutonium and uranium,the distribution of neptunium,the control of process.Due to the high radioactivity of 1AW,which accumulated the most

  15. Acute myeloid leukemia induced by graded reduction of a lineage-specific transcription factor, PU.1.

    Science.gov (United States)

    Rosenbauer, Frank; Wagner, Katharina; Kutok, Jeffery L; Iwasaki, Hiromi; Le Beau, Michelle M; Okuno, Yutaka; Akashi, Koichi; Fiering, Steven; Tenen, Daniel G

    2004-06-01

    Transcription factors are believed to have a dominant role in acute myeloid leukemia (AML). This idea is supported by analysis of gene-knockout mice, which uncovered crucial roles of several transcription factors in normal hematopoiesis, and of individuals with leukemia, in whom transcription factors are frequently downregulated or mutated. However, analysis of knockout animals has not shown a direct link between abrogated transcription factors and the pathogenesis of AML. Sfpi1, encoding the lineage-specific transcription factor PU.1, is indispensable for normal myeloid and lymphoid development. We found that mice carrying hypomorphic Sfpi1 alleles that reduce PU.1 expression to 20% of normal levels, unlike mice carrying homo- or heterozygous deletions of Sfpi1, developed AML. Unlike complete or 50% loss, 80% loss of PU.1 induced a precancerous state characterized by accumulation of an abnormal precursor pool retaining responsiveness to G-CSF with disruption of M- and GM-CSF pathways. Malignant transformation was associated with a high frequency of clonal chromosomal changes. Retroviral restoration of PU.1 expression rescued myeloid differentiation of mutant progenitors and AML blasts. These results suggest that tightly graded reduction, rather than complete loss, of a lineage-indispensable transcription factor can induce AML.

  16. Feasibility study of {sup 235}U and {sup 239}Pu characterization in radioactive waste drums using neutron-induced fission delayed gamma rays

    Energy Technology Data Exchange (ETDEWEB)

    Nicol, T. [CEA, DEN, Cadarache, Nuclear Measurement Laboratory, F-13108 Saint-Paul-lez-Durance (France); FZJ, Institute of Energy and Climate Research – Nuclear Waste Management and Reactor Safety, Wilhelm-Johnen-Straße, d-52425 Jülich (Germany); Pérot, B., E-mail: bertrand.perot@cea.fr [CEA, DEN, Cadarache, Nuclear Measurement Laboratory, F-13108 Saint-Paul-lez-Durance (France); Carasco, C. [CEA, DEN, Cadarache, Nuclear Measurement Laboratory, F-13108 Saint-Paul-lez-Durance (France); Brackx, E. [CEA, DEN, Marcoule, Metallography and Chemical Analysis Laboratory, F-30207 Bagnols-sur-Cèze (France); Mariani, A.; Passard, C. [CEA, DEN, Cadarache, Nuclear Measurement Laboratory, F-13108 Saint-Paul-lez-Durance (France); Mauerhofer, E. [FZJ, Institute of Energy and Climate Research – Nuclear Waste Management and Reactor Safety, Wilhelm-Johnen-Straße, d-52425 Jülich (Germany); Collot, J. [Laboratoire de Physique Subatomique et de Cosmologie, Université Grenoble Alpes, CNRS/IN2P3 Grenoble (France)

    2016-10-01

    This paper reports a feasibility study of {sup 235}U and {sup 239}Pu characterization in 225 L bituminized waste drums or 200 L concrete waste drums, by detecting delayed fission gamma rays between the pulses of a deuterium-tritium neutron generator. The delayed gamma yields were first measured with bare samples of {sup 235}U and {sup 239}Pu in REGAIN, a facility dedicated to the assay of 118 L waste drums by Prompt Gamma Neutron Activation Analysis (PGNAA) at CEA Cadarache, France. Detectability in the waste drums is then assessed using the MCNPX model of MEDINA (Multi Element Detection based on Instrumental Neutron Activation), another PGNAA cell dedicated to 200 L drums at FZJ, Germany. For the bituminized waste drum, performances are severely hampered by the high gamma background due to {sup 137}Cs, which requires the use of collimator and shield to avoid electronics saturation, these elements being very penalizing for the detection of the weak delayed gamma signal. However, for lower activity concrete drums, detection limits range from 10 to 290 g of {sup 235}U or {sup 239}Pu, depending on the delayed gamma rays of interest. These detection limits have been determined by using MCNPX to calculate the delayed gamma useful signal, and by measuring the experimental gamma background in MEDINA with a 200 L concrete drum mock-up. The performances could be significantly improved by using a higher interrogating neutron emission and an optimized experimental setup, which would allow characterizing nuclear materials in a wide range of low and medium activity waste packages.

  17. Isotopic composition and distribution of plutonium in northern South China Sea sediments revealed continuous release and transport of Pu from the Marshall Islands.

    Science.gov (United States)

    Wu, Junwen; Zheng, Jian; Dai, Minhan; Huh, Chih-An; Chen, Weifang; Tagami, Keiko; Uchida, Shigeo

    2014-03-18

    The (239+240)Pu activities and (240)Pu/(239)Pu atom ratios in sediments of the northern South China Sea and its adjacent Pearl River Estuary were determined to examine the spatial and temporal variations of Pu inputs. We clarified that Pu in the study area is sourced from a combination of global fallout and close-in fallout from the Pacific Proving Grounds in the Marshall Islands where above-ground nuclear weapons testing was carried out during the period of 1952-1958. The latter source dominated the Pu input in the 1950s, as evidenced by elevated (240)Pu/(239)Pu atom ratios (>0.30) in a dated sediment core. Even after the 1950s, the Pacific Proving Grounds was still a dominant Pu source due to continuous transport of remobilized Pu from the Marshall Islands, about 4500 km away, along the North Equatorial Current followed by the transport of the Kuroshio current and its extension into the South China Sea through the Luzon Strait. Using a simple two end-member mixing model, we have quantified the contributions of Pu from the Pacific Proving Grounds to the northern South China Sea shelf and the Pearl River Estuary are 68% ± 1% and 30% ± 5%, respectively. This study also confirmed that there were no clear signals of Pu from the Fukushima Daiichi Nuclear Power Plant accident impacting the South China Sea.

  18. 计算机模拟研究Pu4+在人体血浆中的分布%Computer simulation of Pu(Ⅳ) speciation in human blood plasma

    Institute of Scientific and Technical Information of China (English)

    邓冰; 蒋树斌; 董兰; 董亮

    2014-01-01

    A thermodynamic equilibrium models consisted of multi-metal ion and low molecular-weight ligands has been constructed to study the speciation of Pu4+ in human blood plasma and the influences of total concentration of DTPA、CO3 2-and Citrate3- on the speciation. Computer simulation indicated that low concentration of plutonium in plasma fluid with Pu(OH)4(aq)species accumula-ted in liver. Pu4+ form precipitation is difficult to eliminate from the body under the high concentration of plutonium in plasma flu-ids. At the concentrations of DTPA was 2. 5 × 10-5 mol·L-1 , the species of plutonium mainly as negatively charged [ Pu ( OH ) DT-PA]2- and maintain stable. The speciation was at first calculated at pH 5. 0,with the increase of concentration of[Citrate3-],the major species of Pu4+ as[ PuCitrate2 ] 2-and[ PuCitrate]+ which were excreted easily from body. In blood plasma Pu4+ combined with Ca2+、Mg2+ to form[CaHDTPA]2-、[Ca2DTPA]-、[CaDTPA]3-、[MgHDTPA]2-、[MgDTPA]3- when[DTPA]at 4.6×10-5mol· L-1 ,which excrete Pu(Ⅳ) and produce toxic side effects on bone at the same time.%建立了由多种金属离子和小分子配体组成的多相人体血浆热力学平衡模型。模拟研究了Pu4+在血浆的形态分布及二乙三胺五乙酸( DTPA)和CO32-、Citrate3-浓度对细胞液中Pu4+形态分布的影响。血浆中的低浓度Pu(Ⅳ)易以Pu(OH)4(aq)的形态蓄积在肝脏中,钚浓度升高则形成沉淀Pu(OH)4(s)难以排出。在[DTPA]=2.5×10-5mol·L-1时,血浆中水溶性小分子[Pu(OH)DTPA]2-含量达到最高并保持稳定。酸性条件下随着[ Citrate3-]的升高,血浆中Pu4+与Citrate3-结合形成可溶性的[ PuCitrate2]2-和[ PuCitrate]+离子化合物。[DTPA]>4.6×10-5mol·L-1时,血浆中的 DTPA以与 Ca2+、Mg2+结合的[CaHDTPA]2-、[Ca2DTPA]-、[CaDT-PA]3-、[ MgHDTPA]2-、[ MgDTPA]3-小分子结合态为主。

  19. Characteristics and Properties of TiO2/EP-PU Composite

    Directory of Open Access Journals (Sweden)

    Chen Yufei

    2015-01-01

    Full Text Available Polymer matrix of EP-PU was prepared by epoxy resin which was polyurethane toughened, and TCA201 coupling agent was used to modify nano-TiO2, and TiO2/EP-PU composite was synthesized using EP, PU, and TCA201-TiO2. The results of SEM and TEM showed that the surface of TiO2 was coated with TCA201 coupling agent through the bonding between the hydroxyl of nano-TiO2 particle and coupling agent molecules, the interaction would be beneficial to improve compatibility of inorganic and organic phases, and TCA201-TiO2 would disperse evenly in composite and improve performance of composite materials. The mechanical properties, thermal stability, dielectric properties, and breakdown strength of composites were investigated by electronic tensile machine, TGA, dielectric spectrum, and CS2674C type voltage tester. The results indicated that appropriate amount of TCA201-TiO2 could improve mechanical properties, the shear strength of 3 wt%-TiO2/EP-PU reached the maximum value at 27.14 MPa, its thermal decomposition temperature was 397.82°C, enhanced 17.48°C more than that of EP-PU matrix, and its dielectric constant (ε and dielectric loss (tan⁡δ showed 4.27 and 0.02, respectively. Its breakdown field strength was 14 kV/mm. Its performance met the requirement of dielectric materials.

  20. European roe deer antlers as an environmental archive for fallout (236)U and (239)Pu.

    Science.gov (United States)

    Froehlich, M B; Steier, P; Wallner, G; Fifield, L K

    2016-01-01

    Anthropogenic (236)U and (239)Pu were measured in European roe deer antlers hunted between 1955 and 1977 which covers and extends beyond the period of intensive nuclear weapons testing (1954-1962). The antlers were hunting trophies, and hence the hunting area, the year of shooting and the approximate age of each animal is given. Uranium and plutonium are known to deposit in skeletal tissue. Since antler histology is similar to bone, both elements were expected in antlers. Furthermore, roe deer shed their antlers annually, and hence antlers may provide a time-resolved environmental archive for fallout radionuclides. The radiochemical procedure is based on a Pu separation step by anion exchange (Dowex 1 × 8) and a subsequent U purification by extraction chromatography using UTEVA(®). The samples were measured by Accelerator Mass Spectrometry at the VERA facility (University of Vienna). In addition to the (236)U and (239)Pu concentrations, the (240)Pu/(239)Pu isotopic ratios were determined with a mean value of 0.172 ± 0.023 which is in agreement with the ratio of global fallout (∼0.18). Rather high (236)U/(238)U ratios of the order of 10(-6) were observed. These measured ratios, where the (236)U arises only from global fallout, have implications for the use of the (236)U/(238)U ratio as a fingerprint for nuclear accidents or releases from nuclear facilities. Our investigations have shown the potential to use antlers as a temporally resolved archive for the uptake of actinides from the environment.

  1. PU/SBA-15介孔分子筛复合材料的制备及性能研究%Study on Preparation and Properties of PU/Zeolite SBA-15 Composites

    Institute of Scientific and Technical Information of China (English)

    张鑫; 佟玉超; 李海艳; 吕志平

    2013-01-01

    采用预聚法制备聚氨酯(PU)/SBA-15介孔分子筛复合材料,并采用DSC、SEM、DMA和TG等方法对复合材料进行表征.结果表明,PU/SBA-15分子筛复合材料与纯聚氨酯相比,拉伸强度有所提高,耐撕裂性能明显增大;复合材料的耐热性能和耐溶剂性能提高不明显;SBA-15分子筛对聚氨酯软硬段的微相分离影响较小.%The polyurethane(PU)/zeolite SBA-15 composites were prepared by prepolymerization method and characterized by DSC, SEM, DMA and TG. The result showed that, compared with the pure PU, PU/zeolite SBA-15 composites showed an increasing of tensile strength and tear-resistance property. The heat-resistance property and solvent resistance property of PU/zeolite SBA-15 composites were not increased obviously. The zeolite SBA-15 had not the obvious effect for microphase separation of PU hard segments and soft segments.

  2. 45 CFR 74.27 - Allowable costs.

    Science.gov (United States)

    2010-10-01

    ... 45 Public Welfare 1 2010-10-01 2010-10-01 false Allowable costs. 74.27 Section 74.27 Public..., AND COMMERCIAL ORGANIZATIONS Post-Award Requirements Financial and Program Management § 74.27 Allowable costs. (a) For each kind of recipient, there is a particular set of Federal principles...

  3. 28 CFR 100.11 - Allowable costs.

    Science.gov (United States)

    2010-07-01

    ... 28 Judicial Administration 2 2010-07-01 2010-07-01 false Allowable costs. 100.11 Section 100.11 Judicial Administration DEPARTMENT OF JUSTICE (CONTINUED) COST RECOVERY REGULATIONS, COMMUNICATIONS ASSISTANCE FOR LAW ENFORCEMENT ACT OF 1994 § 100.11 Allowable costs. (a) Costs that are eligible...

  4. 20 CFR 633.303 - Allowable costs.

    Science.gov (United States)

    2010-04-01

    ... occupation trained for and at not less than the wage specified in the agreement. (g) Travel costs. (1) The... to the overall administrative cost ceiling. (i) Allowances and reimbursements for board and advisory... grantee per quarter. (2) Allowances and loss of wages. Any individual or family member who is a member of...

  5. 75 FR 4098 - Utility Allowance Adjustments

    Science.gov (United States)

    2010-01-26

    ... URBAN DEVELOPMENT Utility Allowance Adjustments AGENCY: Office of the Chief Information Officer, HUD... are required to advise the Secretary of the need for and request of a new utility allowance for... whether the information will have practical utility; (2) Evaluate the accuracy of the agency's estimate...

  6. 44 CFR 13.22 - Allowable costs.

    Science.gov (United States)

    2010-10-01

    ... uniform cost accounting standards that comply with cost principles acceptable to the Federal agency. ... STATE AND LOCAL GOVERNMENTS Post-Award Requirements Financial Administration § 13.22 Allowable costs. (a... increment above allowable costs) to the grantee or subgrantee. (b) Applicable cost principles. For each...

  7. 32 CFR 33.22 - Allowable costs.

    Science.gov (United States)

    2010-07-01

    ... accounting standards that comply with cost principles acceptable to the Federal agency. ... Post-Award Requirements Financial Administration § 33.22 Allowable costs. (a) Limitation on use of... allowable costs) to the grantee or subgrantee. (b) Applicable cost principles. For each kind of...

  8. 36 CFR 1207.22 - Allowable costs.

    Science.gov (United States)

    2010-07-01

    ... uniform cost accounting standards that comply with cost principles acceptable to the Federal agency. ... GOVERNMENTS Post-Award Requirements Financial Administration § 1207.22 Allowable costs. (a) Limitation on use... increment above allowable costs) to the grantee or subgrantee. (b) Applicable cost principles. For each...

  9. 34 CFR 74.27 - Allowable costs.

    Science.gov (United States)

    2010-07-01

    ... Procedures or uniform cost accounting standards that comply with cost principles acceptable to ED. (b) The... OF HIGHER EDUCATION, HOSPITALS, AND OTHER NON-PROFIT ORGANIZATIONS Post-Award Requirements Financial... principles for determining allowable costs. Allowability of costs are determined in accordance with the...

  10. 5 CFR 180.104 - Allowable claims.

    Science.gov (United States)

    2010-01-01

    ... mobile homes may be allowed only in cases of collision, theft, or vandalism. (5) Money. Claims for money... claimant's supervisor. (4) Mobile homes. Claims may be allowed for damage to or loss of mobile homes and their contents under the provisions of § 180.104(c)(2). Claims for structural damage to mobile...

  11. 38 CFR 49.27 - Allowable costs.

    Science.gov (United States)

    2010-07-01

    ... ADMINISTRATIVE REQUIREMENTS FOR GRANTS AND AGREEMENTS WITH INSTITUTIONS OF HIGHER EDUCATION, HOSPITALS, AND OTHER NON-PROFIT ORGANIZATIONS Post-Award Requirements Financial and Program Management § 49.27 Allowable...-Profit Organizations.” The allowability of costs incurred by institutions of higher education...

  12. 20 CFR 435.27 - Allowable costs.

    Science.gov (United States)

    2010-04-01

    ... AGREEMENTS WITH INSTITUTIONS OF HIGHER EDUCATION, HOSPITALS, OTHER NON-PROFIT ORGANIZATIONS, AND COMMERCIAL ORGANIZATIONS Post-Award Requirements Financial and Program Management § 435.27 Allowable costs. For each kind... Organizations.” (c) Allowability of costs incurred by institutions of higher education is determined...