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  1. Glenwood Springs Vapor Caves Pool & Spa Low Temperature Geothermal...

    Open Energy Info (EERE)

    Vapor Caves Pool & Spa Low Temperature Geothermal Facility Jump to: navigation, search Name Glenwood Springs Vapor Caves Pool & Spa Low Temperature Geothermal Facility Facility...

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

    SciTech Connect (OSTI)

    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.

  3. Economical Production of Pu-238

    SciTech Connect (OSTI)

    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.

  4. Radiation damage and 5f-electron localization of Plutonium compounds: -Pu, PuGa3, and PuAl2 , Corwin H. Booth1

    E-Print Network [OSTI]

    Radiation damage and 5f-electron localization of Plutonium compounds: -Pu, PuGa3, and PuAl2 Yu and pure science, people have been studying various plutonium compounds for decades. Starting in the 1980's

  5. Delayed neutron measurements for Th-232, Np-237, Pu-239, Pu-241 and depleted uranium 

    E-Print Network [OSTI]

    Stone, Joseph C.

    2001-01-01

    The neutron emission rates from five very pure actinide samples (Th-232, Np-237, Pu-239, Pu-241 and depleted uranium) were measured following equilibrium irradiation in fast and thermal neutron fluxes. The relative abundances (alphas) for the first...

  6. The Evolution in Pu Nanocluster Electronic Structure: from Atomicity...

    Office of Scientific and Technical Information (OSTI)

    The Evolution in Pu Nanocluster Electronic Structure: from Atomicity to Three Dimensionality Citation Details In-Document Search Title: The Evolution in Pu Nanocluster Electronic...

  7. Evaluation of Los Alamos National Laboratory (LANL) PU238 Waste...

    Office of Environmental Management (EM)

    Los Alamos National Laboratory (LANL) PU238 Waste Management Practices Evaluation of Los Alamos National Laboratory (LANL) PU238 Waste Management Practices This document was used...

  8. Sources for Pu in near surface air

    SciTech Connect (OSTI)

    Hartmann, G.; Thom, C.; Baechmann, K.

    1989-01-01

    This paper provides evidence that most of the Pu in the near surface air today is due to resuspension. Vertical and particle size distribution in near surface air over a period of three years were measured. The seasonal variations of Pu in air and the influence of meteorological parameters on these variations are shown. Samples were taken before the Chernobyl accident in an area where only Pu fallout from the atmospheric nuclear tests of the early sixties occurs. The comparison of the behavior of Pu with other trace elements, which were also measured, showed similar behavior of Pu and elements like Ca, Ti and Fe in near surface air. This confirms that most Pu is resuspended because the main source for these elements in air is the soil surface. Resuspension factors and resuspension rate are estimated for all measured elements. A resuspension factor of 0.8 X 10(-8) m-1 and a resuspension rate of 0.09 X 10(-9) s-1 is calculated for Pu.

  9. THERMOSTATICS AND KINETICS OF TRANSFORMATIONS IN PU-BASED ALLOYS

    SciTech Connect (OSTI)

    Turchi, P; Kaufman, L; Liu, Z

    2006-06-30

    CALPHAD assessment of the thermodynamic properties of a series of Pu-based alloys is briefly presented together with some results on the kinetics of phase formation and transformations in Pu-Ga alloys.

  10. Complementary Pu Resuspension Study at Palomares, Spain

    SciTech Connect (OSTI)

    Shinn, J

    2002-10-01

    Soil in an area near Palomares, Spain, was contaminated with plutonium as a result of a mid-air collision of U.S. military aircraft in January 1966. The assessment for potential inhalation dose can be found in Iranzo et al., (1987). Long-term monitoring has been used to evaluate remedial actions (Iranzo et al., 1988) and there are many supporting studies of the Pu contamination at Palomares that have been carried out by the Centro de Investigaciones Energeticas, Medioambientales y Tecnologicas (CIEMAT) in Madrid. The purpose of this study is to evaluate the resuspension of Pu from the soil in terms of Pu-concentrations in air and resuspension rates in a complementary investigation to those of CIEMAT but in an intensive short-term field effort. This study complements the resuspension studies of CIEMAT at Palomares with additional information, and with confirmation of their previous studies. Observed mass loadings (M) were an average of 70 mg/m{sup 3} with peaks in the daytime of 130 mg/m{sup 3} and low values at night below 30 {micro}g/m{sup 3}. The Pu-activity of aerosols (A) downwind of plot 2-1 was 0.12 Bq/g and the enhancement factor (E{sub f}) had a value of 0.3, which is low but similar to a typical value of 0.7 for other undisturbed sites. This E{sub f} value may increase further away from ground zero. The particle size distribution of the Pu in air measured by cascade impactors was approximately lognormal with a median aerodynamic diameter of 3.7 {micro}m and a geometric standard deviation of 3.5 in the respirable range. This peak midway between 1 ? m and 10 {micro}m in the respirable range is commonly observed. Daily fluctuations in the Pu concentration in air (C) detected by the UHV were lognormally distributed with a geometric standard deviation of 4.9 indicating that the 98th percentile would be 24 times as high as the median. Downwind of plot 2-1 the mean Pu concentration in air, C, was 8.5 {micro}Bq/m{sup 3}. The resuspension factor (Sf) was 2.4 x 10{sup -10} m{sup -1} and agrees very well with the values between 10{sup -10} m{sup -1} and 10{sup -9} m{sup -1} previously reported. We observed a mean Pu/Am ratio of 7.1 with a relative variation of 30%, which compares well with a mean value of 6.5 for nearby plot 2-2. The resuspension rate (R) was in the middle of the range, 10{sup -11} s{sup -1} to 10{sup -12} s{sup -1} as observed in other stable sites, and indicates low potential for Pu redistribution.

  11. Fabrication of a 238Pu target

    SciTech Connect (OSTI)

    Wu, C Y; Chyzh, A; Kwan, E; Henderson, R; Gostic, J; Carter, D

    2010-11-16

    Precision neutron-induced reaction data are important for modeling the network of isotope production and destruction within a given diagnostic chain. This network modeling has many applications such as the design of advanced fuel cycle for reactors and the interpretation of radiochemical data related to the stockpile stewardship and nuclear forensics projects. Our current funded effort is to improve the neutron-induced reaction data on the short-lived actinides and the specific goal is to improve the neutron capture data on {sup 238}Pu with a half-life of 87.7 years. In this report, the fabrication of a {sup 238}Pu target for the proposed measurement using the DANCE array at LANL is described. The {sup 238}Pu target was fabricated from a sample enriched to 99.35%, acquired from ORNL. A total of 395 {micro}g was electroplated onto both sides of a 3 {micro}m thick Ti foil using a custom-made plating cell, shown in Fig 1. The target-material loaded Ti foil is sandwiched between two double-side aluminized mylar foils with a thickness of 1.4 {micro}m. The mylar foil is glued to a polyimide ring. This arrangement is shown partially in Fig. 2. The assembled target is then inserted into an aluminum container with a wall thickness of 0.76 mm, shown in Fig. 3. A derlin ring is used to keep the target assembly in place. The ends of this cylindrical container are vacuum-sealed by two covers with thin Kapton foils as windows for the beam entrance and exit. Shown in Fig. 4 is details of the arrangement. This target is used for phase I of the proposed measurement on {sup 238}Pu scheduled for Nov 2010 together with the DANCE array to address the safety issues raised by LANL. Shown in Fig. 5 is the preliminary results on the yield spectrum as a function of neutron incident energy with a gate on the total {gamma}-ray energy of equivalent Q value. Since no fission PPAC is employed, the distinction between the capture and fission events cannot be made, which is important for the higher neutron incident energy. However, it indicates that a cross section of less than one barn can be measured. The second phase of this experiment will be carried out in 2011 by assembling a PPAC with the {sup 238}Pu target to extend the measurement to higher neutron incident energies by distinguishing the capture from fission events. The fission cross section becomes dominant for neutron incident energies above 30 keV. This PPAC was developed in FY2010 under the NA22 funding and performed very well for the {sup 239}Pu and {sup 241}Pu measurements. A new {sup 238}Pu target will be fabricated for the phase II measurement using the same electroplating technique.

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

    SciTech Connect (OSTI)

    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).

  13. A=3H (2010PU04)

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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  14. A=3He (2010PU04)

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  15. A=3Li (2010PU04)

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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  16. A=3n (2010PU04)

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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  17. Pu Qian | Photosynthetic Antenna Research Center

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

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  18. Procedure for plutonium determination using Pu(VI) spectra

    SciTech Connect (OSTI)

    Walker, L.F.; Temer, D.J.; Jackson, D.D.

    1996-09-01

    This document describes a simple spectrophotometric method for determining total plutonium in nitric acid solutions based on the spectrum of Pu(VI). Plutonium samples in nitric acid are oxidized to Pu(VI) with Ce(IV) and the net absorbance at the 830 nm peak is measured.

  19. Nuclear magnetic resonance offers new insights into Pu 239

    E-Print Network [OSTI]

    - 1 - Nuclear magnetic resonance offers new insights into Pu 239 May 29, 2012 Nuclear magnetic signal of plutonium 239's unique nuclear magnetic resonance signature has been detected by scientists on the subject, "Observation of 239 Pu Nuclear Magnetic Resonance," was published in the May 18 issue of Science

  20. Surrogate studies of the Pu-Be reaction II

    SciTech Connect (OSTI)

    Hanrahan, R.J. Jr.; Thoma, D.J.; Jacobson, L.A.; Zocco, T.G.; Lowery, J.L.; Pereyra, R.

    1997-09-01

    Unusual circumstances could result in contact between molten Pu and solid Be components. Since intimate contact between Pu and Be results in an intense neutron source via the ({alpha},n) reaction it is very difficult to study the kinetics of the Pu-Be interaction. The published Pu-Be phase diagram is characterized by a single intermetallic compound, PuBe{sub 13} which exists in equilibrium with all of the Pu allotropes, and two eutectics with no measurable solubility range in any of the solid phases. This pattern is known to be followed by all of the rare earths, and some of the actinides. Although most of these phase diagrams are poorly defined in terms of solubility and the location of the eutectics, all have been characterized to the extent of having a single intermetallic compound with a melting point in excess of 1,500 C. Consequently it seems reasonable that by studying the reactions of these other metals with Be, it should be possible to predict kinetics and mechanisms of the Pu-Be interaction using known physical and thermodynamic properties. The most obvious difference between Pu and potential surrogate elements is in their melting points. This is not the most important consideration however due to the presence of the two eutectics in each of the M-Be systems (where M is used to refer to any of the surrogates). In the last meeting of this series the authors reported the results of studies using Yb as a surrogate for Pu. Here they will discuss the results obtained using Sm and Ce and contrast them with the earlier results as well as with Pu-Be experiments conducted using very similar experimental conditions.

  1. Performance of Cladding on MOX Fuel with Low 240Pu/239Pu Ratio

    SciTech Connect (OSTI)

    McCoy, Kevin; Blanpain, Patrick; Morris, Robert Noel

    2014-01-01

    The U.S. Department of Energy has decided to dispose of a portion of its surplus plutonium by reconstituting it into mixed oxide (MOX) fuel and irradiating it in commercial power reactors. As part of fuel qualification, four lead assemblies were manufactured and irradiated to a maximum fuel rod average burnup of 47.3 MWd/kg heavy metal. This was the world s first commercial irradiation of MOX fuel with a 240Pu/239Pu ratio less than 0.10. Five fuel rods with varying burnups and plutonium contents were selected from one of the assemblies and shipped to Oak Ridge National Laboratory for hot cell examination. This paper discusses the results of those examinations with emphasis on cladding performance. Exams relevant to the cladding included visual and eddy current exams, profilometry, microscopy, hydrogen analysis, gallium analysis, and mechanical testing. There was no discernible effect of the type of MOX fuel on the performance of the cladding.

  2. Air concentrations of /sup 239/Pu and /sup 240/Pu and potential radiation doses to persons living near Pu-contaminated areas in Palomares, Spain

    SciTech Connect (OSTI)

    Iranzo, E.; Salvador, S.; Iranzo, C.E.

    1987-04-01

    On 17 January 1966, an accident during a refueling operation resulted in the destruction of an air force KC-135 tanker and a B-52 bomber carrying four thermonuclear weapons. Two weapons, whose parachutes opened, were found intact. The others experienced non-nuclear explosion with some burning and release of the fissile fuel at impact. Joint efforts by the United States and Spain resulted in remedial action and a long-term program to monitor the effectiveness of the cleanup. Air concentrations of /sup 239/Pu and /sup 240/Pu have been continuously monitored since the accident. The average annual air concentration for each location was used to estimate committed dose equivalents for individuals living and working around the air sampling stations. The average annual /sup 239/Pu and /sup 240/Pu air concentrations during the 15-y period corresponding to 1966-1980 and the potential committed dose equivalents for various tissues due to the inhalation of the /sup 239/Pu and /sup 240/Pu average annual air concentration during this period are shown and discussed in the report.

  3. 239Pu Resonance Evaluation for Thermal Benchmark System Calculations

    SciTech Connect (OSTI)

    Leal, Luiz C; Noguere, G; De Saint Jean, C; Kahler, A.

    2013-01-01

    Analyses of thermal plutonium solution critical benchmark systems have indicated a deciency in the 239Pu resonance evaluation. To investigate possible solutions to this issue, the Organisation for Economic Co-operation and Development (OECD) Nuclear Energy Agency (NEA) Working Party for Evaluation Cooperation (WPEC) established Subgroup 34 to focus on the reevaluation of the 239Pu resolved resonance parameters. In addition, the impacts of the prompt neutron multiplication (nubar) and the prompt neutron ssion spectrum (PFNS) have been investigated. The objective of this paper is to present the results of the 239Pu resolved resonance evaluation eort.

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

    SciTech Connect (OSTI)

    Migliori, Albert; Betts, J; Trugman, A; Mielke, C H; Mitchell, J N; Ramos, M; Stroe, I

    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.

  5. Glenwood Springs Amendments | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on QA:QAsource History View New PagesSustainable UrbanKentucky:BoreOpenGilliamOhio: EnergyGlenwillow, Ohio:Amendments Jump

  6. Glenwood, Illinois: Energy Resources | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on QA:QAsource History View New PagesSustainable UrbanKentucky:BoreOpenGilliamOhio: EnergyGlenwillow,

  7. Glenwood, Iowa: Energy Resources | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on QA:QAsource History View New PagesSustainable UrbanKentucky:BoreOpenGilliamOhio: EnergyGlenwillow,Iowa: Energy

  8. DEVELOPMENT PROGRAM FOR PU-238 AQUEOUS RECOVERY PROCESS

    SciTech Connect (OSTI)

    M. PANSOY-HJELVIK; M. REIMUS; ET AL

    2000-10-01

    Aqueous processing is necessary for the removal of impurities from {sup 238}Pu dioxide ({sup 238}PuO{sub 2}) fuel due to unacceptable levels of {sup 234}U and other non-actinide impurities in the scrap fuel. Impurities at levels above General Purpose Heat Source (GPHS) fuel specifications may impair the performance.of the heat sources. Efforts at Los Alamos have focused on developing the bench scale methodology for the aqueous process steps which includes comminution, dissolution, ion exchange, precipitation, and calcination. Recently, work has been performed to qualify the bench scale methodology, to show that the developed process produces pure {sup 238}PuO{sub 2} meeting GPHS fuel specifications. In addition, this work has enabled us to determine how waste volumes may be minimized during full-scale processing. Results of process qualification for the bench scale aqueous recovery operation and waste minimization efforts are presented.

  9. Radiation Damage Effects in Candidate Titanates for Pu Disposition: Zirconolite

    SciTech Connect (OSTI)

    Strachan, Denis M.; Scheele, Randall D.; Buck, Edgar C.; Kozelisky, Anne E.; Sell, Rachel L.; Elovich, Robert J.; Buchmiller, William C.

    2008-01-15

    Specimens of titanate ceramics containing approximately 10 mass% 238Pu were tested to determine the long-term effects of radiation-induced damage from the ? decay of 239Pu that would have been disposed of in the nuclear-waste repository at Yucca Mountain. These tests provided information on the changes in bulk properties such as dimensions, densities, and chemical durability. Although these materials become amorphous at low doses, the specimens remained physically strong. Even after the radiation-induced swelling saturated, the specimens remained physically intact with no evidence for microcracking. Thus, in combination with results reported previously on similar materials, the material remains a physically viable material for the disposition of surplus weapons-grade Pu.

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

    SciTech Connect (OSTI)

    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.

  11. Atomic Structure and Phase Transformations in Pu Alloys

    SciTech Connect (OSTI)

    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. Stabilizing And Packaging Pu Materials Per 3013 At SRS

    SciTech Connect (OSTI)

    STEVE, HENSEL

    2005-01-21

    The Savannah River Site (SRS) began packaging Pu metals into 3013 containers in April, 2003 and oxides in October, 2003. A total of 919 outer 3013 containers were made in the FB-Line at SRS when stabilization and packaging was completed in January, 2005. Experiences, lessons learned, and an overview of packaging activities are presented.

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

    SciTech Connect (OSTI)

    Dziewinska, Krystyna; Peters, Michael A; Martinez, Patrick P; Dziewinski, Jacek J; Pugmire, David L; Trujillo, Stephen M; La Verne, Jake A; Rajesh, P

    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.

  14. Delayed neutron emission measurements for U-235 and Pu-239 

    E-Print Network [OSTI]

    Chen, Yong

    2009-05-15

    The delayed neutron emission rates of U-235 and Pu-239 samples were measured accurately from a thermal fission reaction. A Monte Carlo calculation using the Geant4 code was used to demonstrate the neutron energy independence of the detector used...

  15. Spent Nuclear Fuel Self-Induced XRF to Predict Pu to U Content 

    E-Print Network [OSTI]

    Stafford, Alissa Sarah

    2010-10-12

    Los Alamos National Laboratory LEGe Low Energy Germanium Detector LWR Light Water Reactor MC&A Material Control and Accountability MCNP Monte Carlo N?Particle NDA Nondestructive Assay NRC Nuclear Regulatory Committee NRF... measurements would not reflect the Pu to U ratio measured results. Also, for LWR fuel the Pu content is ~1% whereas for fast reactor fuel the Pu content may be 40%. Bushuev?s work showed that distinguishing Pu x-rays in the spent fuel gamma spectrum...

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

    SciTech Connect (OSTI)

    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 to 95 °C reduced the oxidation rate of Pu(IV) to Pu(VI). For 8.1 M HNO{sub 3} simulated dissolution solutions, at near boiling conditions >35% Pu(VI) was present in 50 h while at 95 °C <10% Pu(VI) was present at 50 h. At near boiling temperatures, eliminating the presence of Cr and varying the HNO{sub 3} concentration in the range of 7–8.5 M had little effect on the rate of conversion of Pu(IV) to Pu(VI). HNO{sub 3} oxidation of Pu(IV) to Pu(VI) in a pure solution has been reported previously. Based on simulated dissolution experiments, this study concluded that dissolving Pu metal at 95°C using a 6 to 10 M HNO{sub 3} solution 0.05–0.2 M KF and 0–2 g/L B could reduce the rate of oxidation of Pu(IV) to Pu(VI) as compared to near boiling conditions. To demonstrate this flowsheet, two small-scale experiments were performed dissolving Pu metal up to 6.75 g/L. No Pu-containing residues were observed in the solutions after cooling. Using Pu metal dissolution rates measured during the experiments and a correlation developed by Holcomb, the time required to completely dissolve a batch of Pu metal in an H-Canyon dissolver using this flowsheet was estimated to require nearly 5 days (120 h). This value is reasonably consistent with an estimate based on the Batch 2 and 3 dissolution times in the 6.1D dissolver and Pu metal dissolution rates measured in this study and by Rudisill et al. Data from the present and previous studies show that the Pu metal dissolution rate decreases by a factor of approximately two when the temperature decreased from boiling (112 to 116°C) to 95°C. Therefore, the time required to dissolve a batch of Pu metal in an H-Canyon dissolver at 95°C would likely double (from 36 to 54 h) and require 72 to 108 h depending on the surface area of the Pu metal. Based on the experimental studies, a Pu metal dissolution flowsheet utilizing 6–10 M HNO{sub 3} containing 0.05–0.2 M KF (with 0–2 g/L B) at 95°C is recommended to reduce the oxidation of Pu(IV) to Pu(VI) as compared to near boiling conditions. The time required to completely di

  17. Bacterial Pu(V) reduction in the absence and presence of Fe(III)?NTA: modeling and experimental approach

    SciTech Connect (OSTI)

    Deo, Randhir P.; Rittmann, Bruce E.; Reed, Donald T. (AZU); (Guam); (LANL)

    2013-01-10

    Plutonium (Pu), a key contaminant at sites associated with the manufacture of nuclear weapons and with nuclear-energy wastes, can be precipitated to 'immobilized' plutonium phases in systems that promote bioreduction. Ferric iron (Fe{sup 3+}) is often present in contaminated sites, and its bioreduction to ferrous iron (Fe{sup 2+}) may be involved in the reduction of Pu to forms that precipitate. Alternately, Pu can be reduced directly by the bacteria. Besides Fe, contaminated sites often contain strong complexing ligands, such as nitrilotriacetic acid (NTA). We used biogeochemical modeling to interpret the experimental fate of Pu in the absence and presence of ferric iron (Fe{sup 3+}) and NTA under anaerobic conditions. In all cases, Shewanella alga BrY (S. alga) reduced Pu(V)(PuO{sub 2}{sup +}) to Pu(III), and experimental evidence indicates that Pu(III) precipitated as PuPO{sub 4(am)}. In the absence of Fe{sup 3+} and NTA, reduction of PuO{sub 2}{sup +} was directly biotic, but modeling simulations support that PuO{sub 2}{sup +} reduction in the presence of Fe{sup 3+} and NTA was due to an abiotic stepwise reduction of PuO{sub 2}{sup +} to Pu{sup 4+}, followed by reduction of Pu{sup 4+} to Pu{sup 3+}, both through biogenically produced Fe{sup 2+}. This means that PuO{sub 2}{sup +} reduction was slowed by first having Fe{sup 3+} reduced to Fe{sup 2+}. Modeling results also show that the degree of PuPO{sub 4(am)} precipitation depends on the NTA concentration. While precipitation out-competes complexation when NTA is present at the same or lower concentration than Pu, excess NTA can prevent precipitation of PuPO{sub 4(am)}.

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

    SciTech Connect (OSTI)

    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.

  19. Neutron Resonance Parameters and Covariance Matrix of 239Pu

    SciTech Connect (OSTI)

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

    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.

  20. Overview of advanced technologies for stabilization of {sup 238}Pu-contaminated waste

    SciTech Connect (OSTI)

    Ramsey, K.B.; Foltyn, E.M.; Heslop, J.M.

    1998-02-01

    This paper presents an overview of potential technologies for stabilization of {sup 238}Pu-contaminated waste. Los Alamos National Laboratory (LANL) has processed {sup 238}PuO{sub 2} fuel into heat sources for space and terrestrial uses for the past several decades. The 88-year half-life of {sup 238}Pu and thermal power of approximately 0.6 watts/gram make this isotope ideal for missions requiring many years of dependable service in inaccessible locations. However, the same characteristic which makes {sup 238}Pu attractive for heat source applications, the high Curie content (17 Ci/gram versus 0.06 Ci/gram for 239{sup Pu}), makes disposal of {sup 238}Pu-contaminated waste difficult. Specifically, the thermal load limit on drums destined for transport to the Waste Isolation Pilot Plant (WIPP), 0.23 gram per drum for combustible waste, is impossible to meet for nearly all {sup 238}Pu-contaminated glovebox waste. Use of advanced waste treatment technologies including Molten Salt Oxidation (MSO) and aqueous chemical separation will eliminate the combustible matrix from {sup 238}Pu-contaminated waste and recover kilogram quantities of {sup 238}PuO{sub 2} from the waste stream. A conceptual design of these advanced waste treatment technologies will be presented.

  1. Thermal Analysis of ZPPR High Pu Content Stored Fuel

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Solbrig, Charles W.; Pope, Chad L.; Andrus, Jason P.

    2014-01-01

    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 themore »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).« less

  2. On Automatic Families Sanjay Jain, Yuh Shin Ong, Shi Pu and Frank Stephan

    E-Print Network [OSTI]

    Stephan, Frank

    On Automatic Families Sanjay Jain, Yuh Shin Ong, Shi Pu and Frank Stephan S. Jain, Y. S. Ong, S. Pu: fstephan@comp.nus.edu.sg This paper summarises previous work on automatic families. It then investigates a natural size measure for members of an automatic family: the size of a member language in the family

  3. Gamma-ray Output Spectra from 239 Pu Fission

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Ullmann, John

    2015-05-25

    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-raymore »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.« less

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

    SciTech Connect (OSTI)

    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 experiments

  5. Radiation Damage Effects in Candidate Titanates for Pu Disposition: Zirconolite

    SciTech Connect (OSTI)

    Strachan, Denis M.; Scheele, Randall D.; Buck, Edgar C.; Kozelisky, Anne E.; Sell, Rachel L.; Elovich, Robert J.; Buchmiller, William C.

    2008-01-15

    This is the second of two papers on the results of radiation-induced damage accumulation in titanate ceramics that potentially could be used for weapons grade plutonium disposition. In the first paper we discussed the results from pyrochlore (betafite) based ceramics. In this paper, we discuss the effects of radiation-induced damage on the density and crystal structure of a nominally phase-pure zirconolite and two other zirconolite-bearing ceramics from the alpha decay of 238Pu. Macro (bulk) and micro (X-ray diffraction) swelling were found to be temperature independent, whereas the density determined with He gas pycnometry was temperature dependent. It took approximately 740 days (2.6?1018 ?/g) for the specimens to become X-ray amorphous—longer for the swelling to saturate. Unlike what we observed for the pyrochlore-based ceramics, we did not observe any phase changes associated with storage temperature and damage ingrowth. The forward dissolution rate at a pH value of 2 for material containing essentially all zirconolite is 1.7(4)?10-3 g/(m2?d). Very little pH dependence was observed for zirconolite specimens and, like we observed for the pyrochlore-bearing ceramics in this study, there was no dependence on the amount of radiation-induced damage. As with the pyrochlore, these materials did not become substantially friable with increasing radiation-induced damage. Even after the radiation-induced swelling saturated, the specimens remained physically intact with no evidence for microcracking. Thus, the material remains physically a viable material for the disposition of surplus weapons-grade Pu.

  6. Studies of vibrational properties in Ga stabilized delta-Pu by extended X-ray absorption fine structure

    SciTech Connect (OSTI)

    Allen, P.G.; Henderson, A.L.; Sylwester, E.R.; Turchi, P.E.A.; Shen, T.H.; Gallegos, G.F.; Booth, C.H.

    2002-02-14

    Temperature dependent extended x-ray absorption fine structure (EXAFS) spectra were measured for a 3.3 at. % Ga stabilized Pu alloy over the range T= 20 - 300 K. EXAFS data were acquired at both the Ga K-edge and the Pu L{sub III} edge. Curve-fits were performed to the first shell interactions to obtain pair-distance distribution widths, {sigma}, as a function of temperature. The temperature dependence of {sigma}(T) was accurately modeled using a correlated-Debye model for the lattice vibrational properties, suggesting Debye-like behavior in this material. Using this formalism, we obtain pair-specific correlated-Debye temperatures, {Theta}{sub cD}, of 110.7 {+-} 1.7 K and 202.6 {+-} 3.7 K, for the Pu-Pu and Ga-Pu pairs, respectively. The result for the Pu-{Theta}{sub cD} value compares well with previous vibrational studies on {delta}-Pu. In addition, our results represent the first unambiguous determination of Ga-specific vibrational properties in Pu-Ga alloys, i.e, {Theta}{sub cD} for the Ga-Pu pair. Because the Debye temperature can be related to a measure of the lattice stiffness, these results indicate the Ga-Pu bonds are significantly stronger than the Pu-Pu bonds. This effect has important implications for lattice stabilization mechanisms in these alloys.

  7. Determining site-specific drum loading criteria for storing combustible {sup 238}Pu waste

    SciTech Connect (OSTI)

    Marshall, R.S.; Callis, E.L.; Cappis, J.H.; Espinoza, J.M.; Foltyn, E.M.; Reich, B.T.; Smith, M.C.

    1994-02-01

    Waste containing hydrogenous-combustible material contaminated with {sup 238}Pu can generate hydrogen gas at appreciable rates through alpha radiolysis. To ensure safe transportation of WIPP drums, the limit for {sup 238}Pu-combustible waste published in the WIPP TRUPACT-11 CONTENT (TRUCON) CODES is 21 milliwafts per 55 gallon drum. This corresponds to about 45 milligrams of {sup 238}PuO{sub 2} used for satellite heat source-electrical generators. The Los Alamos waste storage site adopted a {sup 238}Pu waste storage criteria based on these TRCUCON codes. However, reviews of the content in drums of combustible waste generated during heat source assembly at Los Alamos showed the amount of {sup 238}Pu is typically much greater than 45 milligrams. It is not feasible to appreciably reduce Los Alamos {sup 238}Pu waste drum loadings without significantly increasing waste volumes or introducing unsafe practices. To address this concern, a series of studies were implemented to evaluate the applicability of the TRUCON limits for storage of this specific waste. Addressed in these evaluations were determination of the hydrogen generation rate, hydrogen diffusion rates through confinement layers and vent filters, and packaging requirements specific to Los Alamos generated {sup 238}Pu contaminated combustible waste. These studies also showed that the multiple-layer packaging practices in use at Los Alamos could be relaxed without significantly increasing the risk of contamination. Based on a model developed to predict H{sub 2} concentrations in packages and drum headspace, the site specific effective hydrogen generation rate, and hydrogen-diffusion values, and revising the waste packaging practices, we were able to raise the safe loading limit for {sup 238}Pu waste drums for on site storage to the gram levels typical of currently generated {sup 238}Pu waste.

  8. Magnetic and optical properties of Np and Pu ions and compounds

    SciTech Connect (OSTI)

    Edelstein, N.M.

    1990-08-01

    Three topics are reviewed in this paper. They are the magnetic and optical properties of NpF{sub 6} and PuF{sub 6}, Np(BH{sub 3}CH{sub 3}){sub 4}, and the hyperfine anomaly of {sup 239,241}Pu. Based on recent optical data of NpF{sub 6} and PuF{sub 6} in Ar matrices, new crystal field analyses of these molecules are presented. The temperature dependent {sup 1}H and {sup 11}B NMR shifts of Np(BH{sub 3}CH{sub 3}){sub 4} are discussed. 40 refs., 4 figs., 8 tabs.

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

    SciTech Connect (OSTI)

    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.

  10. Thermophysical properties of ??Pu{sub 2}O{sub 3}: A new potential model

    SciTech Connect (OSTI)

    Günay, S. D. Akdere, Ü.; Ta?seven, Ç.; Akgenç, B.

    2013-12-16

    ??Pu{sub 2}O{sub 3} is an important material among plutonium based materials in nuclear industry. Pure plutonium surfaces quickly oxidizes into ??Pu{sub 2}O{sub 3} and PuO{sub 2} which are in the form of layers one on another. Here we have investigated thermal properties of ??Pu{sub 2}O{sub 3} by molecular dynamics simulation by using a partially ionic semi-empirical rigid ion potential. Mechanical properties, thermal expansion, and heat capacity are calculated. Results were compared with available experimental data and quantum calculation [2]. Due to the experimental limitations such as toxicity and radiation effects, studying the physical properties of such materials from molecular dynamics simulations have vital importance.

  11. PU/SS EUTECTIC ASSESSMENT IN 9975 PACKAGINGS IN A STORAGE FACILITY DURING EXTENDED FIRE

    SciTech Connect (OSTI)

    Gupta, N.

    2012-03-26

    In a radioactive material (RAM) packaging, the formation of eutectic at the Pu/SS (plutonium/stainless steel) interface is a serious concern and must be avoided to prevent of leakage of fissile material to the environment. The eutectic temperature for the Pu/SS is rather low (410 C) and could seriously impact the structural integrity of the containment vessel under accident conditions involving fire. The 9975 packaging is used for long term storage of Pu bearing materials in the DOE complex where the Pu comes in contact with the stainless steel containment vessel. Due to the serious consequences of the containment breach at the eutectic site, the Pu/SS interface temperature is kept well below the eutectic formation temperature of 410 C. This paper discusses the thermal models and the results for the extended fire conditions (1500 F for 86 minutes) that exist in a long term storage facility and concludes that the 9975 packaging Pu/SS interface temperature is well below the eutectic temperature.

  12. COMPUTER SIMULATIONS TO ADDRESS PU-FE EUTECTICISSUE IN 3013 STORAGE VESSEL

    SciTech Connect (OSTI)

    Gupta, N; Allen Smith, A

    2007-03-06

    On November 22, 2005, the Manager of the Plutonium Finishing Plant (PFP) in Richland, WA issued an Occurrence Report involving a potential Pu-Fe eutectic failure mechanism for the stainless steel (SS) 3013 cans containing plutonium (Pu) metal. Four additional reports addressed nuclear safety concerns about the integrity of stainless steel containers holding plutonium during fire scenarios. The reports expressed a belief that the probability and consequences of container failure due to the formation of a plutonium-iron eutectic alloy had been overlooked. Simplified thermal model to address the Pu-Fe eutectic concerns using axisymmetric model similar to the models used in the 9975 SARP were performed. The model uses Rocky Flats configuration with 2 stacked Pu buttons inside a 3013 assembly. The assembly has an outer can, an inner can, and a convenience can, all stainless steel. The boundary conditions are similar to the regulatory 30 minutes HAC fire analyses. Computer simulations of the HAC fire transients lasting 4 hours of burn time show that the interface between the primary containment vessel and the Pu metal in the 9975 package will not reach Pu-Fe eutectic temperature of 400 C.

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

    SciTech Connect (OSTI)

    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.

  14. Am phases in the matrix of a U–Pu–Zr alloy with Np, Am, and rare-earth elements

    SciTech Connect (OSTI)

    Janney, Dawn E.; Kennedy, J. Rory; Madden, James W.; O’Holleran, Thomas P.

    2015-01-01

    Phases and microstructures in the matrix of an as-cast U-Pu-Zr alloy with 3 wt% Am, 2% Np, and 8% rare-earth elements were characterized by scanning and transmission electron microscopy. The matrix consists primarily of two phases, both of which contain Am: ?-(U, Np, Pu, Am) (~70 at% U, 5% Np, 14% Pu, 1% Am, and 10% Zr) and ?-(U, Np, Pu, Am)Zr2 (~25% U, 2% Np, 10-15% Pu, 1-2% Am, and 55-60 at% Zr). These phases are similar to those in U-Pu-Zr alloys, although the Zr content in ?-(U, Np, Pu, Am) is higher than that in ?-(U, Pu) and the Zr content in ?-(U, Np, Pu, Am)Zr2 is lower than that in ?-UZr2. Nanocrystalline actinide oxides with structures similar to UO2 occurred in some areas, but may have formed by reactions with the atmosphere during sample handling. Planar features consisting of a central zone of ?-(U, Np, Pu, Am) bracketed by zones of ?-(U, Np, Pu, Am)Zr2 bound irregular polygons ranging in size from a few micrometers to a few tens of micrometers across. The rest of the matrix consists of elongated domains of ?-(U, Np, Pu, Am) and ?-(U, Np, Pu, Am)Zr2. Each of these domains is a few tens of nanometers across and a few hundred nanometers long. The domains display strong preferred orientations involving areas a few hundred nanometers to a few micrometers across.

  15. Thermal Analysis of ZPPR High Pu Content Stored Fuel

    SciTech Connect (OSTI)

    Charles W. Solbrig; Chad Pope; Jason Andrus

    2014-09-01

    This paper estimates the temperature of high Pu content ZPPR fuel while in storage to determine the probablilty of fuel damage during storage. The Zero Power Physics Reactor (ZPPR) is an experimental reactor which has been decomissioned. It ran only at extremely low power, for testing nuclear reactor designs and was operated as a criticality facility from April 18, 1969 until decommissioned in 1990. Its fuel was manufactured in 1967 and has been in storage since the reactor was decomissioned. Heat is generated in the fuel due to Pu and Am decay and is a concern for possible fuel damage. Any damage to the cladding would be expected to lead to the fuel hydriding and oxidizing over a long period of storage as was described in the analysis of the damage to the ZPPR uranium fuel resulting in the fuel becoming unuseable and a large potential source of contamination. (Ref. Solbrig, 1994). A series of computer runs were made to scope out the range of temperatures that can occur in the ZPPR fuel in storage. The maximum calculated conservative fuel temperature is high (292 degrees C [558 degrees F]) in spite of the fact that the fuel element heat generation rates seem quite low, between 35 and 10 W for containers (called clamshells) full of fuel. However, the ZPPR storage bins, built for safeguards, are very effective insulators. The calculated clamshells and the cavity doors temperatures are also high. No record exists of people receiving skin burns by touching the cavity doors or clamshells, which indicates the computed temperatures may be higher than actual. (Note, gloves are worn when handling hotter clamshells.) Given the high calculated temperatures, a cursory measurement program was conducted to calibrate the calculated results. The measurement of bin doors, cavity doors, and clamshell temperatures would be easy to make if it were not for regulations resulting from security and potential contamination. Due to conservative assumptions in the model like high heat transfer contact resistance between contact surfaces (such as between the fuel and the clamshell), the calculated temperatures are intended to be overestimated. The temperatures of the stored fuel in a particular clamshell are dependent, among other parameters, on the distribution of fuel in the surrounding storage compartments, the heat generation rate of the fuel, and the orientation of fuel in the clamshell (parallel or perpendicular to the door). The distribution of fuel in this analysis was selected to give higher temperatures than actual distributions might give. Due to possible contamination and security concerns, fuel temperatures could not be measured but the bin doors, storage sleeve doors, and clamshell temperatures could be and were measured. The comparison of these three temperatures to the calculations indicates that the temperatures calculated with conservative assumptions are higher than the actual temperatures. This implies that the calculated fuel temperatures are higher than actual also. The maximum calculated fuel temperature with the most conservative assumptions (292 degrees C, (558 degrees F)) is significantly below the no fuel failure criterion of 600 degrees C (1,112 degrees F). Some fuel failures have occurred but these results indicate that the failures are not due to high temperatures encountered in fuel storage.

  16. Recovery of 238PuO2 by Molten Salt Oxidation Processing of 238PuO2 Contaminated Combustibles (Part II)

    SciTech Connect (OSTI)

    Remerowski, Mary Lynn; Dozhier, C.; Krenek, K.; VanPelt, C. E.; Reimus, M. A.; Spengler, D.; Matonic, J.; Garcia, L.; Rios, E.; Sandoval, F.; Herman, D.; Hart, R.; Ewing, B.; Lovato, M.; Romero, J. P. [Los Alamos National Laboratory, Pu-238 Science and Engineering, NMT-9, M/S E502, Los Alamos, NM 87544 (United States)

    2005-02-06

    Pu-238 heat sources are used to fuel radioisotope thermoelectric generators (RTG) used in space missions. The demand for this fuel is increasing, yet there are currently no domestic sources of this material. Much of the fuel is material reprocessed from other sources. One rich source of Pu-238 residual material is that from contaminated combustible materials, such as cheesecloth, ion exchange resins and plastics. From both waste minimization and production efficiency standpoints, the best solution is to recover this material. One way to accomplish separation of the organic component from these residues is a flameless oxidation process using molten salt as the matrix for the breakdown of the organic to carbon dioxide and water. The plutonium is retained in the salt, and can be recovered by dissolution of the carbonate salt in an aqueous solution, leaving the insoluble oxide behind. Further aqueous scrap recovery processing is used to purify the plutonium oxide. Recovery of the plutonium from contaminated combustibles achieves two important goals. First, it increases the inventory of Pu-238 available for heat source fabrication. Second, it is a significant waste minimization process. Because of its thermal activity (0.567 W per gram), combustibles must be packaged for disposition with much lower amounts of Pu-238 per drum than other waste types. Specifically, cheesecloth residues in the form of pyrolyzed ash (for stabilization) are being stored for eventual recovery of the plutonium.

  17. Report on 238Pu(n,x) surrogate cross section measurement

    SciTech Connect (OSTI)

    Burke, J T; Ressler, J J; Henderson, R A; Scielzo, N D; Escher, J E; Thompson, I J; Gostic, J; Bleuel, D; Weideking, M; Bernstein, L A

    2010-03-31

    The goal of this year's effort is to measure the {sup 238}Pu(n,f) and {sup 238}Pu(n,2n) cross section from 100 keV to 20 MeV. We designed a surrogate experiment that used the reaction {sup 239}Pu(a,a{prime}x) as a surrogate for {sup 238}Pu(n,x). The experiment was conducted using the STARS/LIBERACE experimental facility located at the 88 Inch Cyclotron at Lawrence Berkeley National Laboratory in January 2010. A description of the experiment and status of the data analysis is given. In order to obtain a reliable {sup 238}Pu(n,x) cross section we designed the experiment using the surrogate ratio technique. This technique allows one to measure a desired, unknown, cross section relative to a known cross section. In the present example, the {sup 238}Pu(n,x) cross section of interest is determined relative to the known {sup 235}U(n,x) cross section. To increase confidence in the results, and to reduce overall uncertainties, we are also determining the {sup 238}Pu(n,x) cross section relative to the known {sup 234}U(n,x) cross section. The compound nuclei of interest for this experiment were produced using inelastic alpha scattering. For example, {sup 236}U(a,a{prime}x) served as a surrogate for {sup 235}U(n,x); analogous reactions were considered for the other cross sections. Surrogate experiments determine the probabilities for the decay of the compound nuclei into the various channels of interest (fission, gamma decay) by measuring particle-fission (p-f) or particle?gamma (p?g) reaction spectra. By comparing the decay probabilities associated with the unknown cross section to that of a known cross section it is possible to obtain the ratio of these cross sections and thus determine the unknown, desired cross section.

  18. Hematological responses after inhaling {sup 238}PuO{sub 2}: An extrapolation from beagle dogs to humans

    SciTech Connect (OSTI)

    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.

  19. EIS-0299: Proposed Production of Plutonium-238 (Pu-238) for Use in Advanced Radioisotope Power Systems (RPS) for Space Missions

    Broader source: Energy.gov [DOE]

    This EIS is for the proposed production of plutonium-238 (Pu-238) using one or more DOE research reactors and facilities.

  20. Modeling and production of 240Am by deuteron-induced activation of a 240Pu target

    SciTech Connect (OSTI)

    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.

  1. Glenwood Hot Springs Lodge Space Heating Low Temperature Geothermal

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on QA:QAsource History View New PagesSustainable UrbanKentucky:BoreOpenGilliamOhio: EnergyGlenwillow, Ohio:

  2. Glenwood Springs Resource Management Plan (1984) | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on QA:QAsource History View New PagesSustainable UrbanKentucky:BoreOpenGilliamOhio: EnergyGlenwillow, Ohio:Amendments

  3. Glenwood Springs, Colorado: Energy Resources | Open Energy Information

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on QA:QA J-E-1 SECTION J APPENDIX E LISTStar2-0057-EA Jump to:ofEniaElectric Jump to:GerGlacialGlacialGlass

  4. City of Glenwood Springs, Colorado (Utility Company) | Open Energy

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on QA:QA J-E-1 SECTION JEnvironmentalBowerbank,CammackFLIRChurchFontanelle, Iowa (Utility Company)Glen

  5. Comprehensive appraisal of {sup 239+240}Pu in soils around Rocky Flats, Colorado

    SciTech Connect (OSTI)

    Litaor, M.I.; Allen, L.; Ellerbroek, D.

    1995-12-01

    Plutonium contamination of soils around Rocky Flats Environmental & Technology Site, near Golden, Colorado, resulted from past outdoor storage practices and subsequent remobilization due to inadequate cleanup practices. Until now human-health risk assessment has not been performed because of a lack of sufficient information regarding the spatial extent of {sup 239+240}Pu in soils. The purpose of this work was to elucidate the extent of plutonium contamination in surface soils, and to assess the uncertainty associated with the spatial distribution of {sup 239+240}Pu around Rocky Flats Environmental & Technology Site.

  6. Pb-210 and Pu-239,240 in nearshore Gulf of Mexico sediments 

    E-Print Network [OSTI]

    Rotter, Richard Joseph

    1985-01-01

    for this core is unlike either the Pb-210 or Pu plots and shows a relatively steady decrease of activity below 1 cm to approximately 30 cm where Cs-137 activity apparently goes to zero Core 79L316 ? 6 is in slightlv deeper water, 194 m, than core 78G8.... Additional T. nventorv Data from outsidle the Gulf of Mexico. 97 11. Excess Pb-210, Pu, and Cs-137 Inventories 99 12. Calculated Nn Fluxes in the Mississippi Delta. . . . . 105 13. Observed Mn Fluxes in the Ml. ssissiopi Delta 109 LIST OF FIGURES Figure...

  7. Verification of the content, isotopic composition and age of plutonium in Pu-Be neutron sources by gamma-spectrometry

    E-Print Network [OSTI]

    Cong Tam Nguyen

    2005-08-29

    A non-destructive, gamma-spectrometric method for verifying the plutonium content of Pu-Be neutron sources has been developed. It is also shown that the isotopic composition and the age of plutonium (Pu) can be determined in the intensive neutron field of these sources by the ``Multi-Group Analysis'' method. Gamma spectra were taken in the far-field of the sample, which was assumed to be cylindrical. The isotopic composition and the age of Pu were determined using a commercial implementation of the Multi-Group Analysis algorithm. The Pu content of the sources was evaluated from the count rates of the gamma-peaks of 239Pu, relying on the assumption that the gamma-rays are coming to the detector parallel to each other. The determination of the specific neutron yields and the problem of neutron damage to the detector are also discussed.

  8. Understanding oxygen adsorption on 9.375 at. % Ga-stabilized ?-Pu (111) surface: A DFT study

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Hernandez, Sarah C.; Wilkerson, Marianne P.; Huda, Muhammad N.

    2015-08-30

    Plutonium (Pu) metal reacts rapidly in the presence of oxygen (O), resulting in an oxide layer that will eventually have an olive green rust appearance over time. Recent experimental work suggested that the incorporation of gallium (Ga) as an alloying impurity to stabilize the highly symmetric high temperature ?-phase lattice may also provide resistance against corrosion/oxidation of plutonium. In this paper, we modeled a 9.375 at. % Ga stabilized ?-Pu (111) surface and investigated adsorption of atomic O using all-electron density functional theory. Key findings revealed that the O bonded strongly to a Pu-rich threefold hollow fcc site with amore »chemisorption energy of –5.06 eV. Migration of the O atom to a Pu-rich environment was also highly sensitive to the surface chemistry of the Pu–Ga surface; when the initial on-surface O adsorption site included a bond to a nearest neighboring Ga atom, the O atom relaxed to a Ga deficient environment, thus affirming the O preference for Pu. Only one calculated final on-surface O adsorption site included a Ga-O bond, but this chemisorption energy was energetically unfavorable. Chemisorption energies for interstitial adsorption sites that included a Pu or Pu-Ga environment suggested that over-coordination of the O atom was energetically unfavorable as well. Electronic structure properties of the on-surface sites, illustrated by the partial density of states, implied that the Ga 4p states indirectly but strongly influenced the Pu 6d states strongly to hybridize with the O 2p states, while also weakly influenced the Pu 5f states to hybridize with the O 2p states, even though Ga was not participating in bonding with O.« less

  9. Recovery of UO{sub 2}/PuO{sub 2} in IFR electrorefining process

    DOE Patents [OSTI]

    Tomczuk, Z.; Miller, W.E.

    1992-01-01

    This invention is comprised of a process for converting PuO{sub 2} and U0{sub 2} present in an electrorefiner to the chlorides, by contacting the PuO{sub 2} and U0{sub 2} with Li metal in the presence of an alkali metal chloride salt substantially free of rare earth and actinide chlorides for a time and at a temperature sufficient to convert the U0{sub 2} and PuO{sub 2} to metals while converting Li metal to Li{sub 2}O. Li{sub 2}O is removed either by reducing with rare earth metals or by providing an oxygen electrode for transporting 0{sub 2} out of the electrorefiner and a cathode, and thereafter applying an emf to the electrorefiner electrodes sufficient to cause the Li{sub 2}O to disassociate to 0{sub 2} and Li metal but insufficient to decompose the alkali metal chloride salt. The U and Pu and excess lithium are then converted to chlorides by reaction with CdCl{sub 2}.

  10. Optimal power flow in microgrids using event-triggered optimization Pu Wan and Michael D. Lemmon

    E-Print Network [OSTI]

    Lemmon, Michael

    Optimal power flow in microgrids using event-triggered optimization Pu Wan and Michael D. Lemmon Abstract-- Microgrids are power generation and distribution systems in which users and generators-triggered distributed optimization algorithm to solve the optimal power flow (OPF) problem in microgrids. Under event

  11. IN FORMATION PU BLIC ATION SC H EME TITLE Agency plan for The Australian National University

    E-Print Network [OSTI]

    1 | IN FORMATION PU BLIC ATION SC H EME TITLE Agency plan for The Australian National University on its website. It will be directly accessible from the webpage foi.anu.edu.au and be identified possible, provide online content that can be searched by web browsers Provide a search function

  12. Recovery of UO[sub 2]/PuO[sub 2] in IFR electrorefining process

    DOE Patents [OSTI]

    Tomczuk, Z.; Miller, W.E.

    1994-10-18

    A process is described for converting PuO[sub 2] and UO[sub 2] present in an electrorefiner to the chlorides, by contacting the PuO[sub 2] and UO[sub 2] with Li metal in the presence of an alkali metal chloride salt substantially free of rare earth and actinide chlorides for a time and at a temperature sufficient to convert the UO[sub 2] and PuO[sub 2] to metals while converting Li metal to Li[sub 2]O. Li[sub 2]O is removed either by reducing with rare earth metals or by providing an oxygen electrode for transporting O[sub 2] out of the electrorefiner and a cathode, and thereafter applying an emf to the electrorefiner electrodes sufficient to cause the Li[sub 2]O to disassociate to O[sub 2] and Li metal but insufficient to decompose the alkali metal chloride salt. The U and Pu and excess lithium are then converted to chlorides by reaction with CdCl[sub 2].

  13. Recovery of UO.sub.2 /Pu O.sub.2 in IFR electrorefining process

    DOE Patents [OSTI]

    Tomczuk, Zygmunt (Lockport, IL); Miller, William E. (Naperville, IL)

    1994-01-01

    A process for converting PuO.sub.2 and UO.sub.2 present in an electrorefiner to the chlorides, by contacting the PuO.sub.2 and UO.sub.2 with Li metal in the presence of an alkali metal chloride salt substantially free of rare earth and actinide chlorides for a time and at a temperature sufficient to convert the UO.sub.2 and PuO.sub.2 to metals while converting Li metal to Li.sub.2 O. Li.sub.2 O is removed either by reducing with rare earth metals or by providing an oxygen electrode for transporting O.sub.2 out of the electrorefiner and a cathode, and thereafter applying an emf to the electrorefiner electrodes sufficient to cause the Li.sub.2 O to disassociate to O.sub.2 and Li metal but insufficient to decompose the alkali metal chloride salt. The U and Pu and excess lithium are then converted to chlorides by reaction with CdCl.sub.2.

  14. Hidden disorder in the ?'?? transformation of Pu-1.9 at.% Ga

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Jeffries, J. R.; Manley, M. E.; Wall, M. A.; Blobaum, K. J. M.; Schwartz, A. J.

    2012-06-06

    Enthalpy and entropy are thermodynamic quantities critical to determining how and at what temperature a phase transition occurs. At a phase transition, the enthalpy and temperature-weighted entropy differences between two phases are equal (?H=T?S), but there are materials where this balance has not been experimentally or theoretically realized, leading to the idea of hidden order and disorder. In a Pu-1.9 at. % Ga alloy, the ? phase is retained as a metastable state at room temperature, but at low temperatures, the ? phase yields to a mixed-phase microstructure of ?- and ?'-Pu. The previously measured sources of entropy associated withmore »the ?'?? transformation fail to sum to the entropy predicted theoretically. We report an experimental measurement of the entropy of the ?'?? transformation that corroborates the theoretical prediction, and implies that only about 65% of the entropy stabilizing the ? phase is accounted for, leaving a missing entropy of about 0.5 kB/atom. Some previously proposed mechanisms for generating entropy are discussed, but none seem capable of providing the necessary disorder to stabilize the ? phase. This hidden disorder represents multiple accessible states per atom within the ? phase of Pu that may not be included in our current understanding of the properties and phase stability of ?-Pu.« less

  15. Estimates for Pu-239 loadings in burial ground culverts based on fast/slow neutron measurements

    SciTech Connect (OSTI)

    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.

  16. Characterization of U/Pu Particles Originating From the Nuclear Weapon Accidents at Palomares, Spain, 1966 And Thule, Greenland, 1968

    SciTech Connect (OSTI)

    Lind, O.C.; Salbu, B.; Janssens, K.; Proost, K.; Garcia-Leon, M.; Garcia-Tenorio, R.

    2007-07-10

    Following the USAF B-52 bomber accidents at Palomares, Spain in 1966 and at Thule, Greenland in 1968, radioactive particles containing uranium (U) and plutonium (Pu) were dispersed into the environment. To improve long-term environmental impact assessments for the contaminated ecosystems, particles from the two sites have been isolated and characterized with respect to properties influencing particle weathering rates. Low [239]Pu/[235]U (0.62-0.78) and [240]Pu/[239]Pu (0.055-0.061) atom ratios in individual particles from both sites obtained by Inductively Coupled Plasma Mass Spectrometry (ICP-MS) show that the particles contain highly enriched U and weapon-grade Pu. Furthermore, results from electron microscopy with Energy Dispersive X-ray analysis (EDX) and synchrotron radiation (SR) based micrometer-scale X-ray fluorescence ({micro}-XRF) 2D mapping demonstrated that U and Pu coexist throughout the 1-50 {micro}m sized particles, while surface heterogeneities were observed in EDX line scans. SR-based micrometer-scale X-ray Absorption Near Edge Structure Spectroscopy ({micro}-XANES) showed that the particles consisted of an oxide mixture of U (predominately UO[2] with the presence ofU[3][8]) and Pu ((III)/(IV), (V)/(V) or (III), (IV) and (V)). Neither metallic U or Pu nor uranyl or Pu(VI) could be observed. Characteristics such as elemental distributions, morphology and oxidation states are remarkably similar for the Palomares and Thule particles, reflecting that they originate from similar source and release scenarios. Thus, these particle characteristics are more dependent on the original material from which the particles are derived (source) and the formation of particles (release scenario) than the environmental conditions to which the particles have been exposed since the late 1960s.

  17. Separate effects identification via casting process modeling for experimental measurement of U–Pu–Zr alloys

    SciTech Connect (OSTI)

    J. Crapps; D. S. DeCroix; J. D. Galloway; D. A. Korzekwa; R. Aikin; R. Fielding; R. Kennedy; C. Unal

    2013-11-01

    Computational simulations of gravity casting processes for metallic U–Pu–Zr nuclear fuel rods have been performed using a design-of-experiments technique to determine the fluid flow, liquid heat transfer, and solid heat transfer parameters which most strongly influence the process solidification speed and fuel rod porosity. The results are used to make recommendations for the best investment of experimental time and effort to measure process parameters.

  18. Phonon dispersion curves determination in (delta)-phase Pu-Ga alloys

    SciTech Connect (OSTI)

    Wong, J; Clatterbuck, D; Occelli, F; Farber, D; Schwartz, A; Wall, M; Boro, C; Krisch, M; Beraud, A; Chiang, T; Xu, R; Hong, H; Zschack, P; Tamura, N

    2006-02-07

    We have designed and successfully employed a novel microbeam on large grain sample concept to conduct high resolution inelastic x-ray scattering (HRIXS) experiments to map the full phonon dispersion curves of an fcc {delta}-phase Pu-Ga alloy. This approach obviates experimental difficulties with conventional inelastic neutron scattering due to the high absorption cross section of the common {sup 239}Pu isotope and the non-availability of large (mm size) single crystal materials for Pu and its alloys. A classical Born von-Karman force constant model was used to model the experimental results, and no less than 4th nearest neighbor interactions had to be included to account for the observation. Several unusual features including, a large elastic anisotropy, a small shear elastic modulus, (C{sub 11}-C{sub 12})/2, a Kohn-like anomaly in the T{sub 1}[011] branch, and a pronounced softening of the T[111] branch towards the L point in the Brillouin are found. These features may be related to the phase transitions of plutonium and to strong coupling between the crystal structure and the 5f valence instabilities. Our results represent the first full phonon dispersions ever obtained for any Pu-bearing material, thus ending a 40-year quest for this fundamental data. The phonon data also provide a critical test for theoretical treatments of highly correlated 5f electron systems as exemplified by recent dynamical mean field theory (DMFT) calculations for {delta}-plutonium. We also conducted thermal diffuse scattering experiments to study the T(111) dispersion at low temperatures with an attempt to gain insight into bending of the T(111) branch in relationship to the {delta} {yields} {alpha}{prime} transformation.

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

    SciTech Connect (OSTI)

    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.

  20. Type B Accident Investigation on the August 5, 2003, Pu-238 Multiple Uptake

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious RankADVANCEDInstallers/ContractorsPhotovoltaicsStateof Energy TwoEvent at the Pu Facility, Los Alamos

  1. Technical Basis for Safe Operations with Pu-239 in NMS and S Facilities (F and H Areas)

    SciTech Connect (OSTI)

    Bronikowski, M.G.

    1999-03-18

    Plutonium-239 is now being processed in HB-Line and H-Canyon as well as FB-Line and F-Canyon. As part of the effort to upgrade the Authorization Basis for H Area facilities relative to nuclear criticality, a literature review of Pu polymer characteristics was conducted to establish a more quantitative vs. qualitative technical basis for safe operations. The results are also applicable to processing in F Area facilities.The chemistry of Pu polymer formation, precipitation, and depolymerization is complex. Establishing limits on acid concentrations of solutions or changing the valence to Pu(III) or Pu(VI) can prevent plutonium polymer formation in tanks in the B lines and canyons. For Pu(IV) solutions of 7 g/L or less, 0.22 M HNO3 prevents polymer formation at ambient temperature. This concentration should remain the minimum acid limit for the canyons and B lines when processing Pu-239 solutions. If the minimum acid concentration is compromised, the solution may need to be sampled and tested for the presence of polymer. If polymer is not detected, processing may proceed. If polymer is detected, adding HNO3 to a final concentration above 4 M is the safest method for handling the solution. The solution could also be heated to speed up the depolymerization process. Heating with > 4 M HNO3 will depolymerize the solution for further processing.Adsorption of Pu(IV) polymer onto the steel walls of canyon and B line tanks is likely to be 11 mg/cm2, a literature value for unpolished steel. This value will be confirmed by experimental work. Tank-to-tank transfers via steam jets are not expected to produce Pu(IV) polymer unless a larger than normal dilution occurs (e.g., >3 percent) at acidities below 0.4 M.

  2. Ground-state wave function of plutonium in PuSb as determined via x-ray magnetic circular dichroism

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Janoschek, M.; Haskel, D.; Fernandez-Rodriguez, J.; van Veenendaal, M.; Rebizant, J.; Lander, G. H.; Zhu, J. -X.; Thompson, J. D.; Bauer, E. D.

    2015-01-14

    Measurements of x-ray magnetic circular dichroism (XMCD) and x-ray absorption near-edge structure (XANES) spectroscopy at the Pu M?,? edges of the ferromagnet PuSb are reported. Using bulk magnetization measurements and a sum rule analysis of the XMCD spectra, we determine the individual orbital [?L = 2.8(1)?B/Pu] and spin moments [?S = –2.0(1)?B/Pu] of the Pu 5f electrons for the first time. Atomic multiplet calculations of the XMCD and XANES spectra reproduce well the experimental data and are consistent with the experimental value of the spin moment. These measurements of Lz and Sz are in excellent agreement with the values thatmore »have been extracted from neutron magnetic form factor measurements, and confirm the local character of the 5f electrons in PuSb. We demonstrate that a split M? as well as a narrow M? XMCD signal may serve as a signature of 5f electron localization in actinide compounds.« less

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

    SciTech Connect (OSTI)

    Kiedrowski, Brian C.; Conlin, Jeremy Lloyd; Favorite, Jeffrey A.; Kahler, III, Albert C.; Kersting, Alyssa R.; Parsons, Donald K.; Walker, Jessie L.

    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.

  4. First-principles study of the Kondo physics of a single Pu impurity in a Th host

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Zhu, Jian -Xin; Albers, R. C.; Haule, K.; Wills, J. M.

    2015-04-23

    Based on its condensed-matter properties, crystal structure, and metallurgy, which includes a phase diagram with six allotropic phases, plutonium is one of the most complicated pure elements in its solid state. Its anomalous properties, which are indicative of a very strongly correlated state, are related to its special position in the periodic table, which is at the boundary between the light actinides that have itinerant 5f electrons and the heavy actinides that have localized 5f electrons. As a foundational study to probe the role of local electronic correlations in Pu, we use the local-density approximation together with a continuous-time quantummore »Monte Carlo simulation to investigate the electronic structure of a single Pu atom that is either substitutionally embedded in the bulk and or adsorbed on the surface of a Th host. This is a simpler case than the solid phases of Pu metal. With the Pu impurity atom we have found a Kondo resonance peak, which is an important signature of electronic correlations, in the local density of states around the Fermi energy. We show that the peak width of this resonance is narrower for Pu atoms at the surface of Th than for those in the bulk due to a weakened Pu - 5f hybridization with the ligands at the surface.« less

  5. Ground-state wave function of plutonium in PuSb as determined via x-ray magnetic circular dichroism

    SciTech Connect (OSTI)

    Janoschek, M.; Haskel, D.; Fernandez-Rodriguez, J.; van Veenendaal, M.; Rebizant, J.; Lander, G. H.; Zhu, J. -X.; Thompson, J. D.; Bauer, E. D.

    2015-01-01

    Measurements of x-ray magnetic circular dichroism (XMCD) and x-ray absorption near-edge structure (XANES) spectroscopy at the Pu M?,? edges of the ferromagnet PuSb are reported. Using bulk magnetization measurements and a sum rule analysis of the XMCD spectra, we determine the individual orbital [?L = 2.8(1)?B/Pu] and spin moments [?S = ?2.0(1)?B/Pu] of the Pu 5f electrons for the first time. Atomic multiplet calculations of the XMCD and XANES spectra reproduce well the experimental data and are consistent with the experimental value of the spin moment. These measurements of ?Lz? and ?Sz? are in excellent agreement with the values that have been extracted from neutron magnetic form factor measurements, and confirm the local character of the 5f electrons in PuSb. Finally, we demonstrate that a split M? as well as a narrow M? XMCD signal may serve as a signature of 5f electron localization in actinide compounds.

  6. Microsoft Word - ex parte memo deLaski Harris.doc

    Broader source: Energy.gov (indexed) [DOE]

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustmentsShirleyEnergyTher i nAand DOE SafetyofDepartment. " 21Strategies, Inc., JudithFriday,

  7. To: Department of Energy From: Andrew deLaski, Appliance Standards Awareness Project

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious RankADVANCEDInstallers/ContractorsPhotovoltaicsState ofSavings forTitle XVII Final Rule Title2-26 Date:

  8. Stability constants important to the understanding of plutonium in environmental waters, hydroxy and carbonate complexation of PuO{sub 2}{sup +}

    SciTech Connect (OSTI)

    Bennett, D A

    1990-04-20

    The formation constants for the reactions PuO{sub 2}{sup +} + H{sub 2}O = PuO{sub 2}(OH) + H{sup +} and PuO{sub 2}{sup +} + CO{sub 3}{sup 2} = PuO{sub 2}(CO{sub 3}){sup {minus}} were determined in aqueous sodium perchlorate solutions by laser-induced photoacoustic spectroscopy. The molar absorptivity of the PuO{sub 2}{sup +} band at 569 nm decreased with increasing hydroxide concentration. Similarly, spectral changes occurred between 540 and 580 nm as the carbonate concentration was increased. The absorption data were analyzed by the non-linear least-squares program SQUAD to yield complexation constants. Using the specific ion interaction theory, both complexation constants were extrapolated to zero ionic strength. These thermodynamic complexation constants were combined with the oxidation-reduction potentials of Pu to obtain Eh versus pH diagrams. 120 refs., 35 figs., 12 tabs.

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

    SciTech Connect (OSTI)

    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 increased to increase 238Pu production.

  10. Electrodeposition of U and Pu on Thin C and Ti Substrates

    SciTech Connect (OSTI)

    Henderson, R A; Gostic, J M

    2010-05-19

    Physics experiments aimed at deducing key parameters for use in a variety of programs critical to the mission of the National Laboratories require actinide targets placed onto various substrates. The target material quantity and the substrate desired depend upon the type of experiment being designed. The physicist(s) responsible for the experimental campaign will consult with the radiochemistry staff as to the feasibility of producing a desired target/substrate combination. In this report they discuss the production of U and Pu targets on very thin C and Ti substrates. The techniques used, plating cells designed for, tips, and limits is discussed.

  11. Modeling of constituent redistribution in U-Pu-Zr metallic fuel.

    SciTech Connect (OSTI)

    Kim, Y. S.; Hofman, G. L.; Hayes, S. L.; Yacout, A. M.; Nuclear Engineering Division; INL

    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.

  12. DOE plutonium disposition study: Pu consumption in ALWRs. Volume 2, Final report

    SciTech Connect (OSTI)

    Not Available

    1993-05-15

    The Department of Energy (DOE) has contracted with Asea Brown Boveri-Combustion Engineering (ABB-CE) to provide information on the capability of ABB-CE`s System 80 + Advanced Light Water Reactor (ALWR) to transform, through reactor burnup, 100 metric tonnes (MT) of weapons grade plutonium (Pu) into a form which is not readily useable in weapons. This information is being developed as part of DOE`s Plutonium Disposition Study, initiated by DOE in response to Congressional action. This document Volume 2, provides a discussion of: Plutonium Fuel Cycle; Technology Needs; Regulatory Considerations; Cost and Schedule Estimates; and Deployment Strategy.

  13. Microscopic modeling of mass and charge distributions in the spontaneous fission of 240Pu

    E-Print Network [OSTI]

    Jhilam Sadhukhan; Witold Nazarewicz; Nicolas Schunck

    2015-10-27

    In this letter, we outline a methodology to calculate microscopically mass and charge distributions of spontaneous fission yields. We combine the multi-dimensional minimization of collective action for fission with stochastic Langevin dynamics to track the relevant fission paths from the ground-state configuration up to scission. The nuclear potential energy and collective inertia governing the tunneling motion are obtained with nuclear density functional theory in the collective space of shape deformations and pairing. We obtain a quantitative agreement with experimental data and find that both the charge and mass distributions in the spontaneous fission of 240Pu are sensitive both to the dissipation in collective motion and to adiabatic characteristics.

  14. Microscopic modeling of mass and charge distributions in the spontaneous fission of 240Pu

    E-Print Network [OSTI]

    Sadhukhan, Jhilam; Schunck, Nicolas

    2015-01-01

    In this letter, we outline a methodology to calculate microscopically mass and charge distributions of spontaneous fission yields. We combine the multi-dimensional minimization of collective action for fission with stochastic Langevin dynamics to track the relevant fission paths from the ground-state configuration up to scission. The nuclear potential energy and collective inertia governing the tunneling motion are obtained with nuclear density functional theory in the collective space of shape deformations and pairing. We obtain a quantitative agreement with experimental data and find that both the charge and mass distributions in the spontaneous fission of 240Pu are sensitive both to the dissipation in collective motion and to adiabatic characteristics.

  15. Possible experimental evidence for the presence of double octupole states in {sup 240}Pu

    SciTech Connect (OSTI)

    Pascu, S.; Spieker, M.; Bucurescu, D.; Faestermann, T.; Hertenberger, R.; Skalacki, S.; Weber, S.; Wirth, H. F.; Zamfir, N. V.; Zilges, A.

    2012-10-20

    Excited states in the {sup 240}Pu nucleus have been studied by means of the (p,t) reaction using the Q3D spectrometer and the focal plane detector from Munich. The comparison between experimental angular distributions and the DWBA calculations allowed the extraction of relative two-neutron transfer strengths. These observables may reveal important information about the structure of different states. The experimental two neutron strength for the 0{sup +}{sub 2} and 0{sup +}{sub 3} states is found in good agreement with the predictions of the IBA model, confirming the double octupole nature for the 0{sup +}{sub 2} state proposed in the previous studies.

  16. Summary of Puʻu ʻOʻo - Kupaianaha Eruption, Kilauea Volcano, Hawaii |

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page| Open Energy Information Serbia-Enhancing CapacityVectren)Model for the EntireOpen Energy Information Puʻu ʻOʻo

  17. Microsoft Word - Template_SLAC Proprietary Use Agreement_PU 11_14_13

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration wouldMass map shines light on77 PAGE OFDetection of Hydrates7In 1 STEOBTSA ProprietaryJulyPU

  18. Algebra (Informatica) 9 gennaio 2003 Con pi di 18 punti si pu fare l'orale o accettare il voto dello scritto (30 e lode per chi

    E-Print Network [OSTI]

    Catenacci, Roberto

    Algebra (Informatica) ­ 9 gennaio 2003 Con più di 18 punti si può fare l'orale o accettare il voto

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

    SciTech Connect (OSTI)

    Ye, G.A.; Xiao, S.T.; Yan, T.H.; Lin, R.S.; Zhu, Z.W.

    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.

  20. /sup 238/PuO/sub 2//Mo-50 wt% Re compatibility at 800 and 1000/sup 0/C

    SciTech Connect (OSTI)

    Schaeffer, D.R.; Teaney, P.E.

    1980-07-18

    The compatibility of Mo-50 wt % Re with /sup 238/PuO/sub 2/ was investigated after heat treatments of up to 720 days at 800/sup 0/C and 180 days at 1000/sup 0/C. At 800/sup 0/C, a 1-..mu..m thick, continuous layer of molybdenum oxide resulted. At 1000/sup 0/C, the oxide reaction product contained some plutonium and did not appear continuous. At 1000/sup 0/C, a layer of intermetallic formed at the Mo-Re edge, beneath the oxide layer, creating a barrier between the Mo-50 wt % Re and the /sup 238/PuO/sub 2/. The intermetallic layer was promoted by the iron impurity in the /sup 238/PuO/sub 2/.

  1. PLANTS AS BIO-MONITORS FOR 137CS, 238PU, 239, 240PU AND 40K AT THE SAVANNAH RIVER SITE

    SciTech Connect (OSTI)

    Caldwell, E.; Duff, M.; Ferguson, C.

    2010-12-16

    The nuclear fuel cycle generates a considerable amount of radioactive waste, which often includes nuclear fission products, such as strontium-90 ({sup 90}Sr) and cesium-137 ({sup 137}Cs), and actinides such as uranium (U) and plutonium (Pu). When released into the environment, large quantities of these radionuclides can present considerable problems to man and biota due to their radioactive nature and, in some cases as with the actinides, their chemical toxicity. Radionuclides are expected to decay at a known rate. Yet, research has shown the rate of elimination from an ecosystem to differ from the decay rate due to physical, chemical and biological processes that remove the contaminant or reduce its biological availability. Knowledge regarding the rate by which a contaminant is eliminated from an ecosystem (ecological half-life) is important for evaluating the duration and potential severity of risk. To better understand a contaminants impact on an environment, consideration should be given to plants. As primary producers, they represent an important mode of contamination transfer from sediments and soils into the food chain. Contaminants that are chemically and/or physically sequestered in a media are less likely to be bio-available to plants and therefore an ecosystem.

  2. 137Cs(90Sr) and Pu isotopes in the Pacific Ocean sources & trends

    SciTech Connect (OSTI)

    Hamilton, T.F., Millies-Lacrox, J.C. [Service Mixte de Securite Radologique, Mondhery (France); Hong, G.H. [Korea Ocean Research and Development Institute, Ansan (Korea)

    1996-11-01

    The main source of artificial radioactivity in the world`s oceans can be attributed to worldwide fallout from atmospheric nuclear weapons testing. Measurements of selected artificial radionuclides in the Pacific Ocean were first conducted in the 1960`s where it was observed that fallout radioactivity had penetrated the deep ocean. Extensive studies carried out during the 1973-74 GEOSECS provided the first comprehensive data on the lateral and vertical distributions of {sup 9O}Sr, {sup 137}Cs and Pu isotopes in the Pacific on a basin wide scale. Estimates of radionuclide inventories in excess of amounts predicted to be delivered by global fallout alone were attributed to close-in fallout and tropospheric inputs from early U.S. tests conducted on Bikini and Enewetak Atolls in the Equatorial Pacific. In general, levels of fallout radionuclides (including {sup 9O}Sr, {sup 137}Cs and Pu isotopes) in the surface waters of the Pacific Ocean have decreased considerably over the past 4 decades and are now much more homogeneously distributed. Resuspension and the subsequent deposition of fallout radionuclides from previously deposited debris on land has become an important source term for the surface ocean. This can be clearly seen in measurements of fallout radionuclides in mineral aerosols over the Korean Peninsula (Yellow dust events). Radionuclides may also be transported from land to sea in river runoff-these transport mechanisms are more important in the Pacific Ocean where large quantities of river water and suspended sands/fluvial sediments reach the coastal zone. Another unique source of artificial radionuclides in the Pacific Ocean is derived from the slow resolubilization and transport of radionuclides deposited in contaminated lagoon and slope sediments near U.S. and French test sites. Although there is a small but significant flux of artificial radionuclides depositing on the sea floor, > 80% of the total 239, {sup 240}Pu inventory and > 95% of the total {sup 137}Cs inventory remains in the water column. Studies conducted through the 1980`s appear to be consistent with earlier findings and indicate that radionuclide inventories in mid-northern latitudes are at least a factor of two above those expected from global fallout alone. The long term persistence of close-in and/or stratospheric fallout from nuclear weapons testing in the Marshall Islands still appears to be the only plausible explanation for this anomaly.

  3. Radioecologycal study of {sup 239/240}Pu in Bangka Island and Muria Peninsula: Determination of {sup 239/240}Pu in marine sediment and seawater as part of baseline data collecting for sitting of candidates of first Indonesia NPP

    SciTech Connect (OSTI)

    Suseno, Heny; Wisnubroto, Djarot S.

    2014-03-24

    Radioisotope Pu-239/240 are alpha emitting nuclides important indicators of radioactive contamination of the marine environment. Global fallout is the main source of plutonium in the marine environment. There are very limited study on {sup 239/240}Pu in Indonesia coastal environments. The data of this radioisotopes is needed for baseline data of nuclear power plant (NPP) site candidates both in Bangka Island and Muria Peninsula. Bottom sediments play an important role in radioecological studies of the marine environment because a large proportion of radioactive substances entering the sea is adsorbed over time onto suspended particulate matter and deposited in sediments. Plutonium is particle reactive and deposited in marine sediment. Radioisotope {sup 239/240}Pu was determinated by alpha spectrometry after radiochemical procedure that was performed in both water and marine sediment from Bangka Island and Muria Peninsula. The sediment baseline of concentration {sup 239/240}Pu in Bangka Island and Muria Peninsula were range from 0.013 to 0.021 Bq.kg{sup ?1} and 0.018 to 0.024 Bq.kg{sup ?1} respectively. The water baseline concentration this isotope were range from 2.73 to 4.05 mBq.m{sup ?3} and 2.98 to 4.50 mBq.m{sup ?3}.

  4. Isothermal Martensitic and Pressure-Induced ? to ?? Phase Transformations in a Pu-Ga Alloy

    SciTech Connect (OSTI)

    Schwartz, A J; Wall, M A; Farber, D L; Moore, K T; Blobaum, K M

    2007-09-10

    A Pu-2 at.% Ga alloy specimen is slowly compressed to {approx}1 GPa in a large volume moissanite anvil cell to induce the face-centered cubic {delta} to simple monoclinic {alpha}{prime} phase transformation. Optical microscopy, x-ray diffraction, and transmission electron microscopy of the specimen recovered to ambient pressure reveal that the vast majority of the microstructure consists of the {alpha}{prime} phase with grain sizes ranging from 10 nm to several hundred nm, with the remainder being {delta} phase dispersed between the {alpha}{prime} grains. This morphology is in contrast to the transformation product of the low-temperature isothermal martensite in which the lath-shaped {alpha}{prime} particles are {approx}20 {micro}m by 2 {micro}m.

  5. Gamma-ray Output Spectra from 239 Pu Fission

    SciTech Connect (OSTI)

    Ullmann, John [Los Alamos National Laboratory; Schwengner, R.; Zuber, K.

    2015-01-01

    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.

  6. DOE Plutonium Disposition Study: Pu consumption in ALWRs. Volume 1, Final report

    SciTech Connect (OSTI)

    Not Available

    1993-05-15

    The Department of Energy (DOE) has contracted with Asea Brown Boveri-Combustion Engineering (ABB-CE) to provide information on the capability of ABB-CE`s System 80 + Advanced Light Water Reactor (ALWR) to transform, through reactor burnup, 100 metric tonnes (MT) of weapons grade plutonium (Pu) into a form which is not readily useable in weapons. This information is being developed as part of DOE`s Plutonium Disposition Study, initiated by DOE in response to Congressional action. This document, Volume 1, presents a technical description of the various elements of the System 80 + Standard Plant Design upon which the Plutonium Disposition Study was based. The System 80 + Standard Design is fully developed and directly suited to meeting the mission objectives for plutonium disposal. The bass U0{sub 2} plant design is discussed here.

  7. Burnup estimation of fuel sourcing radioactive material based on monitored Cs and Pu isotopic activity ratios in Fukushima N. P. S. accident

    SciTech Connect (OSTI)

    Yamamoto, T.; Suzuki, M.; Ando, Y.

    2012-07-01

    After the severe core damage of Fukushima Dai-Ichi Nuclear Power Station, radioactive material leaked from the reactor buildings. As part of monitoring of radioactivity in the site, measurements of radioactivity in soils at three fixed points have been performed for {sup 134}Cs and {sup 137}Cs with gamma-ray spectrometry and for Pu, Pu, and {sup 240}Pu with {alpha}-ray spectrometry. Correlations of radioactivity ratios of {sup 134}Cs to {sup 137}Cs, and {sup 238}Pu to the sum of {sup 239}Pu and {sup 240}Pu with fuel burnup were studied by using theoretical burnup calculations and measurements on isotopic inventories, and compared with the Cs and Pu radioactivity rations in the soils. The comparison indicated that the burnup of the fuel sourcing the radioactivity was from 18 to 38 GWd/t, which corresponded to that of the fuel in the highest power and, therefore, the highest decay heat in operating high-burnup fueled BWR cores. (authors)

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

    SciTech Connect (OSTI)

    Bowyer, Ted W.; Gesh, Christopher J.; Haas, Derek A.; Hayes, James C.; Mahoney, Lenna A.; Meacham, Joseph E.; Mendoza, Donaldo P.; Olsen, Khris B.; Prinke, Amanda M.; Reid, Bruce D.; Woods, Vincent T.

    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.

  9. Stress and Diffusion in Stored Pu ZPPR Fuel from Alpha Generation

    SciTech Connect (OSTI)

    Charles W. Solbrig; Chad L. Pope; Jason P. Andrus

    2014-07-01

    ZPPR (Zero Power Physics Reactor) is a research reactor that has been used to investigate breeder reactor fuel designs. The reactor has been dismantled but its fuel is still stored there. Of concern are its plutonium containing metal fuel elements which are enclosed in stainless steel cladding with gas space filled with helium–argon gas and welded air tight. The fuel elements which are 5.08 cm by 0.508 cm up to 20.32 cm long (2 in × 0.2 in × 8 in) were manufactured in 1968. A few of these fuel elements have failed releasing contamination raising concern about the general state of the large number of other fuel elements. Inspection of the large number of fuel elements could lead to contamination release so analytical studies have been conducted to estimate the probability of failed fuel elements. This paper investigates the possible fuel failures due to generation of helium in the metal fuel from the decay of Pu and its possible damage to the fuel cladding from metal fuel expansion or from diffusion of helium into the fuel gas space. This paper (1) calculates the initial gas loading in a fuel element and its internal free volume after it has been brought into the atmosphere at ZPPR, (2) shows that the amount of helium generated by decay of Pu over 46 years since manufacture is significantly greater than this initial loading, (3) determines the amount of fuel swelling if the helium stays fixed in the fuel plate and estimates the amount of helium which diffuses out of the fuel plate into the fuel plenum assuming the helium does not remain fixed in the fuel plate but can diffuse to the plenum and possibly through the cladding. Since the literature is not clear as to which possibility occurs, as with Schroedinger’s cat, both possibilities are analyzed. The paper concludes that (1) if the gas generated is fixed in the fuel, then the fuel swelling it can cause would not cause any fuel failure and (2) if the helium does diffuse out of the fuel (in accordance diffusivities estimated from the literature), then it is unlikely that fuel element bulging will occur.

  10. Rational Ligand Design for U(VI) and Pu(IV)

    SciTech Connect (OSTI)

    Szigethy, Geza

    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, UO{sub 2}{sup 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 saturation, these ligands exhibited increased uranyl affinity compared to bis-Me-3,2-HOPO ligands. This result is due in part to their increased denticity, but is primarily the result of the presence of the TAM moiety. In an effort to explore the relatively unexplored coordination chemistry of Pu(IV) with bidentate moieties, a series of Pu(IV) complexes were also crystallized using bidentate hydroxypyridinone and hydroxypyrone ligands. The geometries of these complexes are compared to that of the analogous Ce(IV) complexes. While in some cases these showed the expected structural similarities, some ligand systems led to significant coordination changes. A series of crystal structure analyses with Ce(IV) indicated that these differences are most likely the result of crystallization condition differences and solvent inclusion effects.

  11. Delta/Alpha-Prime Phase Transformations in a Pu-Ga Alloy

    SciTech Connect (OSTI)

    Blobaum, K M; Krenn, C R; Wall, M A; Schwartz, A J

    2005-03-07

    In pure plutonium, the monoclinic {alpha} phase is the equilibrium phase at ambient temperature and pressure. The addition of a few percent of gallium, however, allows the fcc {delta} phase to be retained metastablely at ambient conditions. When the metastable {delta} phase is cooled to subambient temperatures, it partially transforms to the monoclinic {alpha}' phase, which has gallium supersaturated in the lattice. The {alpha}' phase reverts to the {delta} phase when the sample is heated above the ambient temperature. The martensite burst (M{sub b}) and reversion start (R{sub s}) temperatures are functions of the composition, heating rate, and prior thermal history. For a Pu-2.0 at% Ga alloy, the transformation hysteresis is approximately 150 C, which is large compared with other solid-solid phase transformations. Both the forward and reverse transformations are martensitic and proceed via a burst mode. Here, we use differential scanning calorimetry (DSC) and resistometry to perform fundamental studies of the {alpha}'/{delta} transformations with the goal of understanding how aging may affect {delta} phase stability, particularly the M{sub b} temperature. Because materials properties of the {alpha}' and {delta} phases are considerably different (including a density increase of 25% and an accompanying resistivity increase of 46% upon transformation from {delta} to {alpha}'), unexpected transformation to the {alpha}' phase is of particular interest to the stockpile stewardship community.

  12. Density Changes in Plutonium Observed from Accelerated Aging Using Pu-238 Enrichment

    SciTech Connect (OSTI)

    Chung, B W; Thompson, S R; Woods, C H; Hopkins, D J; Gourdin, W H; Ebbinghaus, B B

    2005-10-19

    In support of Stockpile Stewardship activities, accelerated aging tests on a plutonium alloy enriched with 7.3 atomic percentage of {sup 238}Pu is underway using dilatometry at 35, 50, and 65 C and immersion density measurements of material stored at 50 C. Changes in density are expected from radiation damage in the lattice and helium in-growth. After twenty-five equivalent years of aging, the dilatometry data shows that the alloys at 35 C have expanded in volume by 0.11% to 0.12% and have started to exhibit a near linear expansion behavior primarily caused by the helium accumulation. The average He-to-vacancy ratio from tested specimens was determined to be around 2.3. The model for the lattice damage and helium in-growth accurately represents the volume swelling at 35 C. The density converted from the dilatometry corresponds well to the decreasing density trend of reference plutonium alloys as a function of time.

  13. Rapid fusion method for the determination of Pu, Np, and Am in large soil samples

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Maxwell, Sherrod L.; Culligan, Brian; Hutchison, Jay B.; McAlister, Daniel R.

    2015-02-14

    A new rapid sodium hydroxide fusion method for the preparation of 10-20 g soil samples has been developed by the Savannah River National Laboratory (SRNL). The method enables lower detection limits for plutonium, neptunium, and americium in environmental soil samples. The method also significantly reduces sample processing time and acid fume generation compared to traditional soil digestion techniques using hydrofluoric acid. Ten gram soil aliquots can be ashed and fused using the new method in 1-2 hours, completely dissolving samples, including refractory particles. Pu, Np and Am are separated using stacked 2mL cartridges of TEVA and DGA Resin and measuredmore »using alpha spectrometry. The method can be adapted for measurement by inductively-coupled plasma mass spectrometry (ICP-MS). Two 10 g soil aliquots of fused soil may be combined prior to chromatographic separations to further improve detection limits. Total sample preparation time, including chromatographic separations and alpha spectrometry source preparation, is less than 8 hours.« less

  14. Disposition of transuranic residues from plutonium isentropic compression experiment (Pu-ICE) constucted at Z machine

    SciTech Connect (OSTI)

    Goyal, Kapil K [Los Alamos National Laboratory; French, David M [Los Alamos National Laboratory; Humphrey, Betty J [WESTON SOLUTIONS INC.; Gluth, Jeffry [SNL

    2010-01-01

    In 1992, the U.S. Congress passed legislation to discontinue above- and below-ground testing of nuclear weapons. Because of this, the U.S. Department of Energy (DOE) must rely on laboratory experiments and computer-based calculations to verify the reliability of the nuclear stockpile. The Sandia National Laboratories/New Mexico (SNL/NM) Z machine was developed to support the science-based approach for mimicking nuclear explosions and stockpile stewardship. Plutonium (Pu) isotopes with greater than ninety-eight percent enrichment were used in the experiments. In May 2006, SNL/NM received authority that the Z Machine Isentropic Compression Experiments could commence. Los Alamos National Laboratory (LANL) provided the plutonium targets and loaded the target assemblies provided by SNL/NM. Three experiments were conducted from May through July 2006. The residues from each experiment, which weighed up to 913 pounds, were metallic and were packaged into a 55-gallon drum each. SNL/NM conducts the experiments and provides temporary storage for the drums until shipment to LANL for final waste certification for disposal at the Waste Isolation Pilot Plant (WIPP) in southeastern New Mexico. This paper presents a comprehensive approach for documenting generator knowledge for characterization of waste in cooperation with scientists at the two laboratories and addresses a variety of essential topics.

  15. Assessment of a mechanistic model in U-Pu-Zr metallic alloy fuel fission-gas behavior simulations

    SciTech Connect (OSTI)

    Yun, D.; Rest, J.; Yacout, A. M.

    2012-07-01

    A mechanistic kinetic rate theory model originally developed for the prediction of fission gas behavior in oxide nuclear fuels under steady-state and transient conditions has been assessed to look at its applicability to model fission gas behavior in U-Pu-Zr metallic alloy fuel. In order to capture and validate the underlying physics for irradiated U-Pu-Zr fuels, the mechanistic model was applied to the simulation of fission gas release, fission gas and fission product induced swelling, and the evolution of the gas bubble size distribution in three different fuel zones: the outer {alpha}-U, the intermediate, and the inner {gamma}-U zones. Due to its special microstructural features, the {alpha}-U zone in U-Pu-Zr fuels is believed to contribute the largest fraction of fission gas release among the different fuel zones. It is shown that with the use of small effective grain sizes, the mechanistic model can predict fission gas release that is consistent with (though slightly lower than) experimentally measured data. These simulation results are comparable to the experimentally measured fission gas release since the mechanism of fission gas transport through the densely distributed laminar porosity in the {alpha}-U zone is analogous to the mechanism of fission gas transport through the interconnected gas bubble porosity utilized in the mechanistic model. Detailed gas bubble size distributions predicted with the mechanistic model in both the intermediate zone and the high temperature {gamma}-U zone of U-Pu-Zr fuel are also compared to experimental measurements from available SEM micrographs. These comparisons show good agreements between the simulation results and experimental measurements, and therefore provide crucial guidelines for the selection of key physical parameters required for modeling these two zones. In addition, the results of parametric studies for several key parameters are presented for both the intermediate zone and the {gamma}-U zone simulations. (authors)

  16. Quantifying the importance of orbital over spin correlations in delta-Pu within density-functional theory

    SciTech Connect (OSTI)

    Soderlind, P; Wolfer, W

    2007-07-27

    Spin and orbital and electron correlations are known to be important when treating the high-temperature {delta} phase of plutonium within the framework of density-functional theory (DFT). One of the more successful attempts to model {delta}-Pu within this approach has included condensed-matter generalizations of Hund's three rules for atoms, i.e., spin polarization, orbital polarization, and spin-orbit coupling. Here they perform a quantitative analysis of these interactions relative rank for the bonding and electronic structure in {delta}-Pu within the DFT model. The result is somewhat surprising in that spin-orbit coupling and orbital polarization are far more important than spin polarization for a realistic description of {delta}-Pu. They show that these orbital correlations on their own, without any formation of magnetic spin moments, can account for the low atomic density of the {delta} phase with a reasonable equation-of-state. In addition, this unambiguously non-magnetic (NM) treatment produces a one-electron spectra with resonances close to the Fermi level consistent with experimental valence band photoemission spectra.

  17. Short-lived $^{244}$Pu Points to Compact Binary Mergers as Sites for Heavy r-process Nucleosynthesis

    E-Print Network [OSTI]

    Hotokezaka, Kenta; Paul, Michael

    2015-01-01

    Measurements of the radioactive $^{244}$Pu abundances can break the degeneracy between high-rate/low-yield and low-rate/high-yield scenarios for the production of heavy $r$-process elements. The first corresponds to production by core collapse supernovae (cc-SNe) while the latter corresponds to production by e.g. compact binary mergers. The estimated $^{244}$Pu abundance in the current interstellar medium inferred from deep-sea measurements (Wallner et al. 2015) is significantly lower than that corresponding Early Solar System abundances (Turner et al 2007). We estimate the expected median value of the $^{244}$Pu abundances and fluctuations around this value in both models. We show that while the current and Early Solar System abundances are naturally explained within the low-rate/high-yield (e.g. merger) scenario, they are incompatible with the high-rate/low-yield (cc-SNe) model. The inferred event rate remarkably agrees with compact binary merger rates estimated from Galactic neutron star binaries and from ...

  18. Effect of 1-hydroxyethane-1,1-diphosphonic acid (HEDPA) on Partitioning of Np and Pu to Synthetic Boehmite

    SciTech Connect (OSTI)

    Powell, Brian A.; Rao, Linfeng; Nash, Kenneth L.

    2009-05-01

    The effect of 1-hydroxyethane-1,1-diphosphonic acid (HEDPA) on sorption of Np(V) and Pu(V) to synthetic boehmite ({gamma}-AlOOH) was examined a function of time and pH (between 4 to 11). Sorption of both elements in boehmite suspensions (1 M NaCl, 600 mg L{sup -1} boehmite) increased with increasing pH. Sorption edges for neptunium and plutonium occurred at approximately pH 8.0 and 6.6, respectively. After steady state partitioning was reached, HEDPA was added to the neptunium-boehmite and plutonium-boehmite suspensions. Neptunium and plutonium partitioning appears to be primarily affected by the formation of soluble Np:HEDPA and Pu:HEDPA complexes, the dissolution of boehmite promoted by HEDPA, and the precipitation of Np:HEDPA and Pu:HEDPA colloids. The results are discussed in terms of applicability of HEDPA-promoted dissolution as a waste reduction method in the treatment of sludge phases contained within high-level nuclear waste storage tanks.

  19. Modeling of selected ceramic processing parameters employed in the fabrication of 238PuO2 fuel pellets

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Brockman, R. A.; Kramer, D. P.; Barklay, C. D.; Cairns-Gallimore, D.; Brown, J. L.; Huling, J. C.; Van Pelt, C. E.

    2011-10-01

    Recent deep space missions utilize the thermal output of the radioisotope plutonium-238 as the fuel in the thermal to electrical power system. Since the application of plutonium in its elemental state has several disadvantages, the fuel employed in these deep space power systems is typically in the oxide form such as plutonium-238 dioxide (238PuO2). As an oxide, the processing of the plutonium dioxide into fuel pellets is performed via ''classical'' ceramic processing unit operations such as sieving of the powder, pressing, sintering, etc. Modeling of these unit operations can be beneficial in the understanding and control of processing parameters withmore »the goal of further enhancing the desired characteristics of the 238PuO2 fuel pellets. A finite element model has been used to help identify the time-temperature-stress profile within a pellet during a furnace operation taking into account that 238PuO2 itself has a significant thermal output. The results of the modeling efforts will be discussed.« less

  20. Comparison of {sup 241}Am, {sup 239,240}Pu, and {sup 137}Cs concentrations in soil around Rocky Flats

    SciTech Connect (OSTI)

    Hulse, S.E.; Ibrahim, S.A.; Whicker, F.W.; Chapman, P.L.

    1999-03-01

    Gamma spectroscopy measurements were used to estimate concentrations of {sup 241}Am and {sup 137}Cs in soil profiles to depths of 21 cm at on-site and off-site locations around the Rocky Flats Environmental Technology Site and at regional background locations east of the Front Range between Colorado`s borders with New Mexico and Wyoming. Concentrations of these radionuclides were compared with concentrations of {sup 239,240}Pu in the same samples. Concentrations of {sup 241}Am in soil from depths of 0 to 3 cm decreased in an easterly direction from more than 5.3 kBq kg{sup {minus}1} 5 to 7 km away at a rate that was nearly proportional to the inverse square of distance. Deposits of {sup 137}Cs were ubiquitous, averaging 0.12 kBq kg{sup {minus}1} in soil from depths of 0 to 3 cm, but were unevenly distributed around Rocky Flats and the regional background locations. Deviations from the uniform exponential rate at which soil concentrations of {sup 137}Cs typically decreased with depth, {minus}0.25 cm{sup {minus}1} at undisturbed sites, enabled the authors to determine that about 10% of their sampling sites had been disturbed by erosion, tillage, or other factors. The mean rate at which {sup 239,240}Pu decreased with depth was about the same, {minus}0.23 cm{sup {minus}1}, throughout the study area. Soil concentrations of {sup 241}Am decreased with depth at a similar mean rate of {minus}0.22 cm{sup {minus}1} at locations close to the 903 pad where measurements were robust. Ratios between {sup 241}Am or {sup 239,240}Pu and {sup 137}Cs proved more useful for delineating the extent and pattern of contamination from Rocky Flats than did activity concentrations in soil.

  1. TRISO-Fuel Element Performance Modeling for the Hybrid LIFE Engine with Pu Fuel Blanket

    SciTech Connect (OSTI)

    DeMange, P; Marian, J; Caro, M; Caro, A

    2010-02-18

    A TRISO-coated fuel thermo-mechanical performance study is performed for the hybrid LIFE engine to test the viability of TRISO particles to achieve ultra-high burnup of a weapons-grade Pu blanket. Our methodology includes full elastic anisotropy, time and temperature varying material properties for all TRISO layers, and a procedure to remap the elastic solutions in order to achieve fast fluences up to 30 x 10{sup 25} n {center_dot} m{sup -2} (E > 0.18 MeV). In order to model fast fluences in the range of {approx} 7 {approx} 30 x 10{sup 25} n {center_dot} m{sup -2}, for which no data exist, careful scalings and extrapolations of the known TRISO material properties are carried out under a number of potential scenarios. A number of findings can be extracted from our study. First, failure of the internal pyrolytic carbon (PyC) layer occurs within the first two months of operation. Then, the particles behave as BISO-coated particles, with the internal pressure being withstood directly by the SiC layer. Later, after 1.6 years, the remaining PyC crumbles due to void swelling and the fuel particle becomes a single-SiC-layer particle. Unrestrained by the PyC layers, and at the temperatures and fluences in the LIFE engine, the SiC layer maintains reasonably-low tensile stresses until the end-of-life. Second, the PyC creep constant, K, has a striking influence on the fuel performance of TRISO-coated particles, whose stresses scale almost inversely proportional to K. Obtaining more reliable measurements, especially at higher fluences, is an imperative for the fidelity of our models. Finally, varying the geometry of the TRISO-coated fuel particles results in little differences in the scope of fuel performance. The mechanical integrity of 2-cm graphite pebbles that act as fuel matrix has also been studied and it is concluded that they can reliable serve the entire LIFE burnup cycle without failure.

  2. Disposition of transuranic residues from plutonium isentropic compression experiment (Pu-ice) conducted at Z machine

    SciTech Connect (OSTI)

    Goyal, Kapil K [Los Alamos National Laboratory; French, David M [Los Alamos National Laboratory; Humphrey, Betty J [WESTON SOLUTIONS INC.; Gluth, Jeffry [SNL

    2010-01-01

    In 1992, the U.S. Congress passed legislation to discontinue above- and below-ground testing of nuclear weapons. Because of this, the U.S. Department of Energy (DOE) must rely on laboratory experiments and computer-based calculations to verify the reliability of the nation's nuclear stockpile. The Sandia National Laboratories/New Mexico (SNL/NM) Z machine was developed by the DOE to support its science-based approach to stockpile stewardship. SNL/NM researchers also use the Z machine to test radiation effects on various materials in experiments designed to mimic nuclear explosions. Numerous components, parts, and materials have been tested. These experiments use a variety of radionuclides; however, plutonium (Pu) isotopes with greater than ninety-eight percent enrichment are the primary radionuclides used in the experiments designed for stockpile stewardship. In May 2006, SNL/NM received authority that the Z Machine Isentropic Compression Experiments could commence. Los Alamos National Laboratory (LANL) provided the plutonium targets and loaded the target assemblies, which were fabricated by SNL/NM. LANL shipped the loaded assemblies to SNL/NM for Z machine experiments. Three experiments were conducted from May through July 2006. The residues from each experiment, which weighed up to 913 pounds, were metallic and packaged into a respective 55-gallon drum each. Based on a memorandum of understanding between the two laboratories, LANL provides the plutonium samples and the respective radio-isotopic information. SNL/NM conducts the experiments and provides temporary storage for the drums until shipment to LANL for final waste certification for disposal at the Waste Isolation Pilot Plant (WIPP) in southeastern New Mexico. This paper presents a comprehensive approach for documenting generator knowledge for characterization of waste in cooperation with scientists at the two laboratories and addresses a variety of topics such as material control and accountability, safeguards of material, termination of safeguards for eventual shipment from SNL/NM to LANL, associated approvals from DOE-Carlsbad Field Office, which governs WIPP and various notifications. It portrays a comprehensive approach needed for successful completion of a complex project between two national laboratories.

  3. Full-length U-xPu-10Zr (x=0, 8, 19 wt%) Fast Reactor Fuel Test in FFTF

    SciTech Connect (OSTI)

    D. L. Porter; H.C. Tsai

    2012-08-01

    The Integral Fast Reactor-1 (IFR-1) experiment performed in the Fast Flux Test Facility (FFTF) was the only U-Pu-10Zr (Pu-0, 8 and 19 wt%) metallic fast reactor test with commercial-length (91.4 cm active fuel column length) conducted to date. With few remaining test reactors there is little opportunity for performing another test with a long active fuel column. The assembly was irradiated to the goal burnup of 10 at.%. The beginning of life (BOL) peak cladding temperature of the hottest pin was 608?C, cooling to 522?C at end of life (EOL). Selected fuel pins were examined non destructively using neutron radiography, precision axial gamma scanning, and both laser and spiral contact cladding profilometry. Destructive exams included plenum gas pressure, volume, and gas composition determinations on a number of pins followed by optical metallography, electron probe microanalysis (EPMA), and alpha and beta gamma autoradiography on a single U-19Pu-10Zr pin. The post-irradiation examinations (PIEs) showed very few differences compared to the short-pin (34.3 cm fuel column) testing performed on fuels of similar composition in Experimental Breeder Reactor-II (EBR-II). The fuel column grew axially slightly less than observed in the short pins, but with the same pattern of decreasing growth with increasing Pu content. There was a difference in the fuel-cladding chemical interaction (FCCI) in that the maximum cladding penetration by interdiffusion with fuel/fission products did not occur at the top of the fuel column where the cladding temperature is highest, as observed in EBR-II tests. Instead, the more exaggerated fission-rate profile of the FFTF pins resulted in a peak FCCI at ~0.7 X/L axial location along the fuel column. This resulted from a lower production of rare earth fission products higher in the fuel column as well as a much smaller delta-T between fuel center and cladding, and therefore less FCCI, despite the higher cladding temperature. This behavior could actually help extend the life of a fuel pin in a “long pin” reactor design to a higher peak fuel burnup.

  4. Algebra (Informatica) 24 marzo 2004 Con pi`u di 18 punti si pu`o fare l'orale o accettare il voto dello scritto (30 e lode per chi

    E-Print Network [OSTI]

    Catenacci, Roberto

    Algebra (Informatica) ­ 24 marzo 2004 Con pi`u di 18 punti si pu`o fare l'orale o accettare il voto

  5. Algebra (Informatica) 22 giugno 2004 Con 18 o pi`u punti si pu`o fare l'orale o accettare il voto dello scritto (30 e lode per chi risolve

    E-Print Network [OSTI]

    Catenacci, Roberto

    Algebra (Informatica) ­ 22 giugno 2004 Con 18 o pi`u punti si pu`o fare l'orale o accettare il voto

  6. Atmospheric deposition, resuspension, and root uptake of Pu in corn and other grain-producing agroecosystems near a nuclear fuel facility

    SciTech Connect (OSTI)

    Pinder, J.E. III; McLeod, K.W.; Adriano, D.C.; Corey, J.C.; Boni, A.L. (Savannah River Ecology Laboratory, Aiken, SC (USA))

    1990-12-01

    Plutonium released to the environment may contribute to dose to humans through inhalation or ingestion of contaminated foodstuffs. Plutonium contamination of agricultural plants may result from interception and retention of atmospheric deposition, resuspension of Pu-bearing soil particles to plant surfaces, and root uptake. Plutonium on vegetation surfaces may be transferred to grain surfaces during mechanical harvesting. Data obtained from corn grown near the U.S. Department of Energy's H-Area nuclear fuel chemical separations facility on the Savannah River Site were used to estimate parameters of a simple model of Pu transport in agroecosystems. The parameter estimates for corn were compared to those previously obtained for wheat and soybeans. Despite some differences in parameter estimates among crops, the relative importances of atmospheric deposition, resuspension, and root uptake were similar among crops. For even small deposition rates, the relative importances of processes for Pu contamination of corn grain should be: transfer of atmospheric deposition from vegetation surfaces to grain surfaces during combining greater than resuspension of soil to grain surfaces greater than root uptake. Approximately 3.9 X 10(-5) of a year's atmospheric deposition is transferred to grain. Approximately 6.2 X 10(-9) of the Pu inventory in the soil is resuspended to corn grain, and a further 7.3 X 10(-10) of the soil Pu inventory is absorbed and translocated to grains.

  7. Isothermal Martensitic and Pressure-Induced Delta to Alpha-Prime Phase Transformations in a Pu-Ga Alloy

    SciTech Connect (OSTI)

    Schwartz, A J; Wall, M A; Farber, D L; Moore, K T; Blobaum, K M

    2008-01-18

    A well-homogenized Pu-2 at.% Ga alloy can be retained in the metastable face-centered cubic {delta} phase at room temperature. Ultimately, this metastable {delta} phase will decompose via a eutectoid transformation to the thermodynamically stable monoclinic {alpha} phase and the intermetallic compound Pu{sub 3}Ga over a period of approximately 10,000 years [1]. In addition, these low solute-containing {delta}-phase Pu alloys are metastable with respect to an isothermal martensitic phase transformation to the {alpha}{prime} phase during low temperature excursions [2, 3] and are also metastable with respect to a {delta} {yields} {alpha}{prime} phase transformation with increases in pressure [3-5]. The low temperature {delta} {yields} {alpha}{prime} isothermal martensitic phase transformation in the Pu-2 at.% Ga alloy only goes to {approx}25% completion with the resultant {approx}20 {micro}m long by 2 {micro}m wide lath-shaped {alpha}{prime} particles dispersed within the {delta} matrix. In recently reported studies, Faure et al. [4] have observed a {delta} {yields} {gamma} {yields} {alpha}{prime} pressure-induced phase transformation sequence during a diamond anvil cell investigation and, based on x-ray diffraction and density and compressibility experiments, Harbur [5] has concluded that both {alpha}{prime} and an amorphous phase are present in samples that were pressurized and recovered. In this work, a large volume moissanite anvil cell is constructed to permit the pressurization and recovery of specimens of a size suitable for TEM and electron diffraction studies. The cell, shown in Fig. 1, has an overall diameter of 101.6 mm, a moissanite anvil diameter of 9.00 mm, a culet size of 3 mm, and a spring steel gasket 0.5 mm thick with a hole diameter of 2.5 mm. A 2.3 mm diameter by 100 {micro}m thick sample of {delta}-phase Pu-2 at.% Ga is compressed at a rate of approximately 0.05 GPa/minute to {approx}1 GPa to induce the phase transformation to {alpha}{prime}. Optical microscopy of the recovered specimen reveals a very fine microstructure that appears to be single phase, although the resolution of this technique is insufficient to differentiate between single and multiple phases if the grain size is below approximately 1 {micro}m. X-ray diffraction, using a laboratory Cu K{sub {alpha}} source with wavelength of 1.542{angstrom}, shows the monoclinic reflections from the {alpha}{prime} phase, strong peaks from the aluminum specimen holder, and weak peaks from the face-centered cubic {delta} phase as shown in Fig. 2. The recovered specimen is prepared for TEM and electron diffraction studies as described in Moore et al. [6]. TEM reveals small regions of {delta} phase with a very high dislocation density interspersed between the 10-100's nm {alpha}{prime} grains as shown in Fig. 3. Electron diffraction, shown in the insert in Fig. 3, clearly reveals the presence of the {delta} phase. This microstructure is in contrast to the {alpha}{prime} particles that form as a result of the low-temperature isothermal martensite in which the {alpha}{prime} particles are lath-shaped and significantly larger as shown in the optical micrograph in Fig. 4 of a sample cooled to -120 C and held for 10 hours. In these preliminary results, there is no evidence of either an amorphous phase, as suggested by Harbur [5], or the presence of a {gamma} phase. We expected to observe an amorphous phase based on the similarity of this experiment to that of Harbur [5]. It is possible that the {gamma} phase, as reported by Faure et al. [4], does form as an intermediate, but it is not retained to ambient pressure.

  8. Analysis of Pu-Only Partitioning Strategies in LMFBR Fuel Cycles

    SciTech Connect (OSTI)

    Samuel Bays; Gilles Youinou

    2013-02-01

    Sodium cooled Fast Reactors (SFR) have been under consideration for production of electricity, fissile material production, and for destruction of transuranics for decades. The neutron economy of a SFR can be operated in one of two ways. One possibility is to operate the reactor in a transuranic burner mode which has been the focus of active R&D in the last 15 years. However, prior to that the focus was on breeding transuranics. This later mode of managing the neutron economy relies on ensuring the maximum fuel utilization possible in such a way as to maximize the amount of plutonium produced per unit of fission energy in the reactor core. The goal of maximizing plutonium production in this study is as fissile feed stock for the production of MOX fuel to be used in Light Water Reactors (LWR). Throughout the l970’s, this fuel cycle scenario was the focus of much research by the Atomic Energy Commission in the event that uranium supplies would be scarce. To date, there has been sufficient uranium to supply the once through nuclear fuel cycle. However, interest in a synergistic relationship Liquid Metal Fast Breeder Reactors (LMFBR) and a consumer LWR fleet persists, prompting this study. This study considered LMFBR concepts with varying additions of axial and radial reflectors. Three scenarios were considered in collaboration with a companion study on the LWR-MOX designs based on plutonium nuclide vectors produced by this study. The first scenario is a LMFBR providing fissile material to make MOX fuel where the MOX part of the fuel cycle is operated in a once-through-then-out mode. The second scenario is the same as the first but with the MOX part of the fuel cycle multi-recycling its own plutonium with LMFBR being used for the make-up feed. In these first two scenarios, plutonium partitioning from the minor actinides (MA) was assumed. Also, the plutonium management strategy of the LMFBR ensured that only the high fissile purity plutonium bred from blankets was sold to the MOX LWRs. The third scenario considered a LMFBR fuel cycle in an expansionary mode where excess bred transuranic material is accumulated for spinning off additional LMFBR cores. In this latter scenario, no plutonium partitioning was considered. After every cycle, transuranic from both driver and blankets is sold to the MOX LWRs. The MA production from LMFBR operated in a Pu-only fuel cycle is roughly only 1% that of the transuranic production rate. This is in contrast to LWR fuel cycles where the MA content in TRU is closer to 10% or more. If such a LMFBR were operated to provide fissile material to a fleet of MOX reactors, then 1 GWe of LMFBR could support between approximately 0.11 and 0.43 GWe of LWR-MOX reactors for a LMFBR conversion ratio between 1.1 and 1.5, if the MOX reactors were operated in a once-through-then out mode. If the plutonium is continuously recycled in the MOX reactors then the support ratio is approximately 1 GWe of LMFBR for between 0.13 and 0.65 GWe of LWR-MOX reactors depending on the LMFBR conversion ratio. Also, it was found that if the LMFBR fleet were operated in a purely expansionary mode, the smallest doubling time achievable would be seven years.

  9. Bradley University Student Health Center 819 N. Glenwood Ave Markin Center, Peoria, IL 61625

    E-Print Network [OSTI]

    Nanyes, Ollie

    -EINSTEIN CONDENSATION IN AN ATOMIC GAS WITH ATTRACTIVE INTERACTIONS Authors: Bradley, CC, Sackett, CA, Tollett, JJ OF LIMITED CONDENSATE NUMBER Authors: Bradley, CC, Sackett, CA, Hulet, RG Journal: PHYSICAL REVIEW LETTERS

  10. Glenwood Hot Springs Hotel Pool & Spa Low Temperature Geothermal Facility |

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on QA:QAsource History View New PagesSustainable UrbanKentucky:BoreOpenGilliamOhio: EnergyGlenwillow, Ohio: EnergyOpen

  11. Glenwood Springs Vapor Caves Pool & Spa Low Temperature Geothermal Facility

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on QA:QAsource History View New PagesSustainable UrbanKentucky:BoreOpenGilliamOhio: EnergyGlenwillow, Ohio:Amendments|

  12. Relativistic energy density functionals: Low-energy collective states of {sup 240}Pu and {sup 166}Er

    SciTech Connect (OSTI)

    Li, Z. P.; Niksic, T.; Vretenar, D.; Ring, P.; Meng, J.

    2010-06-15

    The empirical relativistic density-dependent, point-coupling energy density functional, adjusted exclusively to experimental binding energies of a large set of deformed nuclei with Aapprox =150-180 and Aapprox =230-250, is tested with spectroscopic data for {sup 166}Er and {sup 240}Pu. Starting from constrained self-consistent triaxial relativistic Hartree-Bogoliubov calculations of binding energy maps as functions of the quadrupole deformation in the beta-gamma plane, excitation spectra and E2 transition probabilities are calculated as solutions of the corresponding microscopic collective Hamiltonian in five dimensions for quadrupole vibrational and rotational degrees of freedom and compared with available data on low-energy collective states.

  13. Test plan for non-radioactive testing of vertical calciner for development of direct denitration conversion of Pu-bearing liquors to stable, storage solids

    SciTech Connect (OSTI)

    Fisher, F.D.

    1995-03-30

    Plutonium-bearing liquors, including ANL scrap liquors, will be used for development and demonstration of a vertical calciner direct denitration process for conversion of those liquors to stable, storable PuO{sub 2}-rich solids. This test plan is to test with non-radioactive stand-in materials to demonstrate adequate performance of the vertical calciner and ancillary equipment.

  14. Properties measurements of (U{sub 0.7}Pu{sub 0.3})O{sub 2-x} in PO{sub 2}-controlled atmosphere

    SciTech Connect (OSTI)

    Kato, M.; Murakami, T.; Sunaoshi, T.; Nelson, A.T.; McClellan, K.J.

    2013-07-01

    The investigation of physical properties of uranium and plutonium mixed oxide (MOX) fuels is important for the development of fast reactor fuels. It is well known that MOX is a nonstoichiometric oxide, and the physical properties change drastically with the Oxygen-to-Metal (O/M) ratio. A control technique for O/M ratio was established for measurements of high temperature properties of uranium and plutonium mixed oxide fuels. Sintering behavior, thermal expansion and O/M change of (U{sub 0.7}Pu{sub 0.3})O{sub 2.00} and (U{sub 0.7}Pu{sub 0.3})O{sub 1.99} were investigated in PO{sub 2}-controlled atmosphere which was controlled by H{sub 2}/H{sub 2}O gas system. Sintering behavior changed drastically with O/M ratio, and shrinkage of (U{sub 0.7}Pu{sub 0.3})O{sub 2.00} was faster and more advanced at lower temperatures as compared with (U{sub 0.7}Pu{sub 0.3})O{sub 1.99}. Thermal expansion was observed to be slightly increased with decreasing O/M ratio. (authors)

  15. LWR spent fuel reduction by the removal of U and the compact storage of Pu with FP for long-term nuclear sustainability

    SciTech Connect (OSTI)

    Fukasawa, T.; Hoshino, K. [Hitachi-GE Nuclear Energy, Ltd, 3-1-1 Saiwai, Hitachi, Ibaraki, 317-0073 (Japan); Takano, M. [Japan Atomic Energy Agency, 3-1-1 Saiwai, Hitachi, Ibaraki, 317-0073 (Japan); Sato, S. [Hokkaido University, 3-1-1 Saiwai, Hitachi, Ibaraki, 317-0073 (Japan); Shimazu, Y. [Fukui University, 3-1-1 Saiwai, Hitachi, Ibaraki, 317-0073 (Japan)

    2013-07-01

    Fast breeder reactors (FBR) nuclear fuel cycle is needed for long-term nuclear sustainability while preventing global warming and maximum utilizing the limited uranium (U) resources. The 'Framework for Nuclear Energy Policy' by the Japanese government on October 2005 stated that commercial FBR deployment will start around 2050 under its suitable conditions by the successive replacement of light water reactors (LWR) to FBR. Even after Fukushima Daiichi Nuclear Power Plant accident which made Japanese tendency slow down the nuclear power generation activities, Japan should have various options for energy resources including nuclear, and also consider the delay of FBR deployment and increase of LWR spent fuel (LWR-SF) storage amounts. As plutonium (Pu) for FBR deployment will be supplied from LWR-SF reprocessing and Japan will not possess surplus Pu, the authors have developed the flexible fuel cycle initiative (FFCI) for the transition from LWR to FBR. The FFCI system is based on the possibility to stored recycled materials (U, Pu)temporarily for a suitable period according to the FBR deployment rate to control the Pu demand/supply balance. This FFCI system is also effective after the Fukushima accident for the reduction of LWR-SF and future LWR-to-FBR transition. (authors)

  16. CALORIMETER-BASED ADJUSTMENT OF MULTIPLICITY DETERMINED 240PU EFF KNOWN-A ANALYSIS FOR THE ASSAY OF PLUTONIUM

    SciTech Connect (OSTI)

    Dubose, F.

    2012-02-21

    In nuclear material processing facilities, it is often necessary to balance the competing demands of accuracy and throughput. While passive neutron multiplicity counting is the preferred method for relatively fast assays of plutonium, the presence of low-Z impurities (fluorine, beryllium, etc.) rapidly erodes the assay precision of passive neutron counting techniques, frequently resulting in unacceptably large total measurement uncertainties. Conversely, while calorimeters are immune to these impurity effects, the long count times required for high accuracy can be a hindrance to efficiency. The higher uncertainties in passive neutron measurements of impure material are driven by the resulting large (>>2) {alpha}-values, defined as the ({alpha},n):spontaneous fission neutron emission ratio. To counter impurity impacts for high-{alpha} materials, a known-{alpha} approach may be adopted. In this method, {alpha} is determined for a single item using a combination of gamma-ray and calorimetric measurements. Because calorimetry is based on heat output, rather than a statistical distribution of emitted neutrons, an {alpha}-value determined in this way is far more accurate than one determined from passive neutron counts. This fixed {alpha} value can be used in conventional multiplicity analysis for any plutonium-bearing item having the same chemical composition and isotopic distribution as the original. With the results of single calorimeter/passive neutron/gamma-ray measurement, these subsequent items can then be assayed with high precision and accuracy in a relatively short time, despite the presence of impurities. A calorimeter-based known-{alpha} multiplicity analysis technique is especially useful when requiring rapid, high accuracy, high precision measurements of multiple plutonium bearing items having a common source. The technique has therefore found numerous applications at the Savannah River Site. In each case, a plutonium (or mixed U/Pu) bearing item is divided into multiple containers. A single item from that batch is then selected for both neutron and calorimetric measurements; all remaining items undergo a neutron measurement only. Using the technique mentioned above, the 'true' {alpha} value determined from the first (calorimeter and passive neutron measured) item is used in multiplicity analysis for all other items in the batch. The justification for using this {alpha} value in subsequent calculations is the assumption that the chemical composition and isotopic distribution of all batch items are the same, giving a constant ({alpha},n):spontaneous fission ratio. This analysis method has been successfully applied to the KIS Facility, significantly improving measurement uncertainties and reducing processing times for numerous items. Comprehensive plans were later developed to extend the use of this method to other applications, including the K-Area Shuffler and the H-Area Pu-Blending Project. While only the feasibility study for the Shuffler has been completed, implementation of the method in the H-Area Pu-Blending Project is currently in progress and has been successfully applied to multiple items. This report serves to document the details of this method in order to serve as a reference for future applications. Also contained herein are specific examples of the application of known-{alpha} multiplicity analysis.

  17. Study of Pu consumption in light water reactors: Evaluation of GE advanced boiling water reactor plants, compilation of Phase 1C task reports

    SciTech Connect (OSTI)

    Not Available

    1994-01-15

    This report summarizes the evaluations conducted during Phase 1C of the Pu Disposition Study have provided further results which reinforce the conclusions reached during Phase 1A & 1B: These conclusions clearly establish the benefits of the fission option and the use of the ABWR as a reliable, proven, well-defined and cost-effective means available to disposition the weapons Pu. This project could be implemented in the near-term at a cost and on a schedule being validated by reactor plants currently under construction in Japan and by cost and schedule history and validated plans for MOX plants in Europe. Evaluations conducted during this phase have established that (1) the MOX fuel is licensable based on existing criteria for new fuel with limited lead fuel rod testing, (2) that the applicable requirements for transport, handling and repository storage can be met, and (3) that all the applicable safeguards criteria can be met.

  18. On the Potential for Vacancy Annihilation as a Mechanism for Conditioning in Pu-1.9 at.% Ga

    SciTech Connect (OSTI)

    Jeffries, J R; Blobaum, K M; Schwartz, A J

    2009-03-09

    The {delta} {yields} {alpha}{prime} martensitic transformation in Pu-1.9 at.% Ga occurs when the alloy is cooled below about -100 C. This transformation exhibits anomalous behavior, where the isothermal transformation proceeds atypically with double-C kinetics. Recent work has revealed that an ambient temperature isothermal hold (referred to as conditioning) prior to the transformation has different effects depending on whether transformation proceeds in the upper- or lower-C of the double-C: the amount of transformation is increased with conditioning in the upper-C, while the transformation in the lower-C seems to be engendered by conditioning. The mechanism by which conditioning affects the low-temperature {delta} {yields} {alpha}{prime} transformation is thus of great importance to understanding the transformation itself as well as the general circumstances that can affect a martensitic phase transformation. Using differential scanning calorimetry measurements, vacancy annihilation as a mechanism for the conditioning effect has been examined. While there are some characteristics of the conditioning effect that are reminiscent of vacancy annihilation, the results of these experiments suggest that vacancy annihilation is not a likely candidate description for the conditioning effect.

  19. Theoretical aspects of the magnetism in the ferromagnetic A Fe sub 2 systems ( A =U, Np, Pu, and Am)

    SciTech Connect (OSTI)

    Eriksson, O.; Johansson, B. ); Brooks, M.S.S. )

    1990-05-01

    We report on spin-polarized energy-band calculations for the cubic Laves-phase systems UFe{sub 2}, NpFe{sub 2}, PuFe{sub 2}, and AmFe{sub 2}. The calculations were performed with the local-density approximation for the exchange and correlation potential together with a term that shifts the one-electron eigenvalues and takes into account the different interelectronic repulsions for electrons with different 5{ital f} magnetic quantum numbers. The spin-orbit interaction was also included in the band Hamiltonian. Thus the parameter-free calculations incorporate Hund's first, second, and third rules. The magnetism in the first three compounds was found to be dominated by a large orbital contribution coupled antiparallel to the spin moment. In the calculations for AmFe{sub 2}, the 5{ital f} electrons were treated as core electrons. The magnetism was here found to behave very much like the magnetism of similar rare-earth Laves-phase compounds.

  20. International Workshop on Gamma Spectrometry Analysis Codes for U and Pu Isotopics: Workshop Results and Next Steps

    SciTech Connect (OSTI)

    McGinnis, Brent R; Solodov, Alexander A; Shipwash, Jacqueline L; Zhernosek, Alena V; McKinney, Teressa L; Pickett, Chris A; Peerani, Paolo

    2009-01-01

    In November 2008, the Institute of Nuclear Materials Management (INMM) and the European Safeguards Research and Development Association (ESARDA) co-hosted the International Workshop on Gamma Spectrometry Analysis Codes for U and Pu Isotopics at the Oak Ridge National Laboratory (ORNL). This workshop was conducted in response to needs expressed by the international safeguards community to understand better the capabilities and limitations of the codes; to ensure these codes are sustained; and to ensure updates or revisions are performed in a controlled manner. The workshop was attended by approximately 100 participants. The participants included code developers, code suppliers, safeguards specialists, domestic and international inspectors, process operators, regulators, and programme sponsors from various government agencies. The workshop provided a unique opportunity for code developers, commercial distributors and end users to interact in a hands-on laboratory environment to develop solutions for programmatic and technical issues associated with the various codes. The workshop also provided an international forum for discussing development of an internationally accepted standard test method. This paper discusses the organization of the workshop, its goals and objectives and feedback received from the participants. The paper also describes the significance of the working group's contribution to improving codes that are commonly used during inspections to verify that nuclear facilities are compliant with treaty obligations that ensure nuclear fuel cycle facilities are used for peaceful purposes.

  1. The study of synchronous (by local time) changes of the statistical properties of thermal noise and alpha-activity fluctuations of a 239-Pu sample

    E-Print Network [OSTI]

    A. V. Kaminsky; S. E. Shnoll

    2006-05-06

    Experimentally obtained and analyzed fine structure of statistical distributions for two physically independent processes: alpha-decay rate fluctuations of Pu-239 sample in Pushchino (Moscow region, Russia) and equilibrium voltage fluctuations (Johnson noise) from metal-film resistor in Tbilisi (Georgia). Special investigation of histograms shape similarity in these processes demonstrated majority of previously studied effects, called - macroscopic fluctuations. Offered qualitative model of the observed effects.

  2. Modeling of Selected Ceramic Processing Parameters Employed in the Fabrication of 238PuO2 Fuel Pellets

    SciTech Connect (OSTI)

    Brockman, R. A. [Univ. of Dayton, OH (United States); Kramer, Daniel P. [Univ. of Dayton, OH (United States); Barklay, Chadwick D. [Univ. of Dayton, OH (United States); Cairns-Gallimore, Dirk [U.S. Department of Energy, Germantown, MD (United States); Brown, J. L. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Huling, J. C. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); van Pelt, C. E. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2011-01-01

    Recent deep space missions utilize the thermal output of the radioisotope plutonium-238 as the fuel in the thermal to electrical power system. Since the application of plutonium in its elemental state has several disadvantages, the fuel employed in these deep space power systems is typically in the oxide form such as plutonium-238 dioxide (238PuO2). As an oxide, the processing of the plutonium dioxide into fuel pellets is performed via ''classical'' ceramic processing unit operations such as sieving of the powder, pressing, sintering, etc. Modeling of these unit operations can be beneficial in the understanding and control of processing parameters with the goal of further enhancing the desired characteristics of the 238PuO2 fuel pellets. A finite element model has been used to help identify the time-temperature-stress profile within a pellet during a furnace operation taking into account that 238PuO2 itself has a significant thermal output. Results of the modeling efforts will be discussed.

  3. Heavy element radionuclides (Pu, Np, U) and {sup 137}Cs in soils collected from the Idaho National Engineering and Environmental Laboratory and other sites in Idaho, Montana, and Wyoming

    SciTech Connect (OSTI)

    Beasley, T.M.; Rivera, W. Jr. [Dept. of Energy, New York, NY (United States). Environmental Measurements Lab.; Kelley, J.M.; Bond, L.A. [Pacific Northwest National Lab., Richland, WA (United States); Liszewski, M.J. [Bureau of Reclamation (United States); Orlandini, K.A. [Argonne National Lab., IL (United States)

    1998-10-01

    The isotopic composition of Pu in soils on and near the Idaho National Engineering and Environmental Laboratory (INEEL) has been determined in order to apportion the sources of the Pu into those derived from stratospheric fallout, regional fallout from the Nevada Test Site (NTS), and facilities on the INEEL site. Soils collected offsite in Idaho, Montana, and Wyoming were collected to further characterize NTS fallout in the region. In addition, measurements of {sup 237}Np and {sup 137}Cs were used to further identify the source of the Pu from airborne emissions at the Idaho Chemical Processing Plant (ICPP) or fugitive releases from the Subsurface Disposal Area (SDA) in the Radioactive Waste Management Complex (RWMC). There is convincing evidence from this study that {sup 241}Am, in excess of that expected from weapons-grade Pu, constituted a part of the buried waste at the SDA that has subsequently been released to the environment. Measurements of {sup 236}U in waters from the Snake River Plain aquifer and a soil core near the ICPP suggest that this radionuclide may be a unique interrogator of airborne releases from the ICPP. Neptunium-237 and {sup 238}Pu activities in INEEL soils suggest that airborne releases of Pu from the ICPP, over its operating history, may have recently been overestimated.

  4. Delayed Fission Gamma-ray Characteristics of Th-232 U-233 U-235 U-238 and Pu-239

    SciTech Connect (OSTI)

    Lane, Taylor; Parma, Edward J.

    2015-08-01

    Delayed fission gamma-rays play an important role in determining the time dependent ioniz- ing dose for experiments in the central irradiation cavity of the Annular Core Research Reactor (ACRR). Delayed gamma-rays are produced from both fission product decay and from acti- vation of materials in the core, such as cladding and support structures. Knowing both the delayed gamma-ray emission rate and the time-dependent gamma-ray energy spectrum is nec- essary in order to properly determine the dose contributions from delayed fission gamma-rays. This information is especially important when attempting to deconvolute the time-dependent neutron, prompt gamma-ray, and delayed gamma-ray contribution to the response of a diamond photo-conducting diode (PCD) or fission chamber in time frames of milliseconds to seconds following a reactor pulse. This work focused on investigating delayed gamma-ray character- istics produced from fission products from thermal, fast, and high energy fission of Th-232, U-233, U-235, U-238, and Pu-239. This work uses a modified version of CINDER2008, a transmutation code developed at Los Alamos National Laboratory, to model time and energy dependent photon characteristics due to fission. This modified code adds the capability to track photon-induced transmutations, photo-fission, and the subsequent radiation caused by fission products due to photo-fission. The data is compared against previous work done with SNL- modified CINDER2008 [ 1 ] and experimental data [ 2 , 3 ] and other published literature, includ- ing ENDF/B-VII.1 [ 4 ]. The ability to produce a high-fidelity (7,428 group) energy-dependent photon fluence at various times post-fission can improve the delayed photon characterization for radiation effects tests at research reactors, as well as other applications.

  5. Evaluation of the ²³?Pu prompt fission neutron spectrum induced by neutrons of 500 keV and associated covariances

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Neudecker, D.; Talou, P.; Kawano, T.; Smith, D. L.; Capote, R.; Rising, M. E.; Kahler, A. C.

    2015-08-01

    We present evaluations of the prompt fission neutron spectrum (PFNS) of ²³?Pu induced by 500 keV neutrons, and associated covariances. In a previous evaluation by Talou et al. 2010, surprisingly low evaluated uncertainties were obtained, partly due to simplifying assumptions in the quantification of uncertainties from experiment and model. Therefore, special emphasis is placed here on a thorough uncertainty quantification of experimental data and of the Los Alamos model predicted values entering the evaluation. In addition, the Los Alamos model was extended and an evaluation technique was employed that takes into account the qualitative differences between normalized model predicted valuesmore »and experimental shape data. These improvements lead to changes in the evaluated PFNS and overall larger evaluated uncertainties than in the previous work. However, these evaluated uncertainties are still smaller than those obtained in a statistical analysis using experimental information only, due to strong model correlations. Hence, suggestions to estimate model defect uncertainties are presented, which lead to more reasonable evaluated uncertainties. The calculated keff of selected criticality benchmarks obtained with these new evaluations agree with each other within their uncertainties despite the different approaches to estimate model defect uncertainties. The keff one standard deviations overlap with some of those obtained using ENDF/B-VII.1, albeit their mean values are further away from unity. Spectral indexes for the Jezebel critical assembly calculated with the newly evaluated PFNS agree with the experimental data for selected (n,?) and (n,f) reactions, and show improvements for high-energy threshold (n,2n) reactions compared to ENDF/B-VII.1.« less

  6. Fission Product Yields of {sup 233}U, {sup 235}U, {sup 238}U and {sup 239}Pu in Fields of Thermal Neutrons, Fission Neutrons and 14.7-MeV Neutrons

    SciTech Connect (OSTI)

    Laurec, J.; Adam, A.; Bruyne, T. de [Commissariat a l'Energie Atomique, Centre DAM-Ile de France (CEA DAM DIF), 91297 Arpajon (France); Bauge, E., E-mail: eric.bauge@cea.f [Commissariat a l'Energie Atomique, Centre DAM-Ile de France (CEA DAM DIF), 91297 Arpajon (France); Granier, T.; Aupiais, J.; Bersillon, O.; Le Petit, G. [Commissariat a l'Energie Atomique, Centre DAM-Ile de France (CEA DAM DIF), 91297 Arpajon (France); Authier, N.; Casoli, P. [Commissariat a l'Energie Atomique, Centre de Valduc, 21120 Is-sur-Tille (France)

    2010-12-15

    The yields of more than fifteen fission products have been carefully measured using radiochemical techniques, for {sup 235}U(n,f), {sup 239}Pu(n,f) in a thermal spectrum, for {sup 233}U(n,f), {sup 235}U(n,f), and {sup 239}Pu(n,f) reactions in a fission neutron spectrum, and for {sup 233}U(n,f), {sup 235}U(n,f), {sup 238}U(n,f), and {sup 239}Pu(n,f) for 14.7 MeV monoenergetic neutrons. Irradiations were performed at the EL3 reactor, at the Caliban and Prospero critical assemblies, and at the Lancelot electrostatic accelerator in CEA-Valduc. Fissions were counted in thin deposits using fission ionization chambers. The number of fission products of each species were measured by gamma spectrometry of co-located thick deposits.

  7. Measurement/Evaluation Techniques and Nuclear Data Associated with Fission of 239Pu by Fission Spectrum Neutrons

    SciTech Connect (OSTI)

    Baisden, P; Bauge, E; Ferguson, J; Gilliam, D; Granier, T; Jeanloz, R; McMillan, C; Robertson, D; Thompson, P; Verdon, C; Wilkerson, C; Young, P

    2010-03-16

    This Panel was chartered to review and assess new evaluations of work on fission product data, as well as the evaluation process used by the two U.S. nuclear weapons physics laboratories. The work focuses on fission product yields resulting from fission spectrum neutrons incident on plutonium, and includes data from measurements that had not been previously published as well as new or revised fission product cumulative yield data, and related quantities such as Q values and R values. This report documents the Panel's assessment of the work presented by Los Alamos National Laboratory (LANL) and Lawrence Livermore National Laboratory (LLNL). Based on the work presented we have seven key observations: (1) Experiments conducted in the 1970s at LANL, some of which were performed in association with a larger, NIST-led, program, have recently been documented. A preliminary assessment of this work, which will be referred to in this document as ILRR-LANL, shows it to be technically sound. (2) LLNL has done a thorough, unbiased review and evaluation of the available literature and is in the process of incorporating the previously unavailable LANL data into its evaluation of key fission product yields. The results of the LLNL effort, which includes a preliminary evaluation of the ILRR-LANL data, have been documented. (3) LANL has also conducted an evaluation of fission product yields for fission spectrum neutrons on plutonium including a meta-analysis of benchmark data as part of a planned upgrade to the ENDF/B compilation. We found that the approach of using meta-analysis provides valuable additional insight for evaluating the sparse data sets involved in this assessment. (4) Both laboratories have provided convincing evidence for energy dependence in the fission product yield of {sup 147}Nd produced from the bombardment of {sup 239}Pu with fission spectrum neutrons over an incident neutron energy range of 0.2 to 1.9 MeV. (5) Consistent, complete, and explicit treatment of both systematic and statistical uncertainties, including correlations, are critical to the assessment of both the experimental measurements (due to variations between experimental techniques, irradiation conditions, calibration procedures, etc.), and the evaluation of those experiments to extract fundamental nuclear data. A clear example of the importance of uncertainty analysis is in the justification for energy-dependent {sup 147}Nd fission product yield, where the magnitude of the effect is comparable to the uncertainties of the individual fission product yield measurements. Both LANL and LLNL are committed to the inclusion of full uncertainty analysis in their evaluations. (6) The Panel reviewed in detail two methods for determining/evaluating fission product yields from which fission assessments can be made: the K factor method and high-resolution gamma spectroscopy (both described more fully in Sections 3 and 4). The panel concluded that fission product yields, and thus fission assessments, derived using either approach are equally valid, provided that the data were obtained from well understood, direct fission measurements and that the key underlying calibrations and/or data are valid for each technique. (7) The Panel found the process of peer review of the two complementary but independent methods to be an extremely useful exercise. Although work is still ongoing and the numbers presented to the Panel may change slightly, both groups are now in much better agreement on not just one, but four key fission product yields. The groups also have a better appreciation of the strengths and weaknesses of each other's methods.

  8. Supporting evidence for double-C curve kinetics in the isothermal (delta) --> (alpha)' phase transformation in a Pu-Ga alloy

    SciTech Connect (OSTI)

    Oudot, B; Blobaum, K M; Wall, M A; Schwartz, A J

    2006-07-21

    Time-temperature-transformation (TTT) diagrams for the {delta} {yields} {alpha}{prime} transformation in a number of Pu-Ga alloys were first reported in 1975 by Orme et al. Unlike typical single-C curve kinetics observed in most isothermal martensitic transformations, the Pu-1.9 at.% Ga alloy exhibits two noses, and thus double-C curve kinetics. The authors attributed the occurrence of the double C to a difference in mechanism: a massive transformation for the upper C and a martensitic transformation for the lower C. Since that time, the nature, and the existence of the double C have received only limited attention. The results of Deloffre et al. suggest a confirmation of this behavior, but the fundamental origin of the double C remains unknown. Here, we apply differential scanning calorimetry (DSC) as an alternative approach to acquiring the TTT data and our experimental evidence suggests a confirmation of the double-C behavior after 18 hours of isothermal hold time. In addition, we report three exothermic peaks corresponding to transformations during cooling at 20 C/min prior to the isothermal holds. These three peaks are reproducible and suggest a number of possibilities for the origin of the unique kinetics: {alpha}{prime} forms with different morphologies, or from different embryos in the upper and lower C curves; {alpha}{prime} forms directly in one C curve and forms via an intermediate phase in the other C curve; the two C curves result from {alpha}{prime} forming by two or more distinct mechanisms (e.g., massive and martensitic transformations).

  9. LONG-TERM SALINITY PREDICTION WITH UNCERTAINTY ANALYSIS: APPPLI-CATION FOR THE COLORADO RIVER NEAR GLENWOOD SPRINGS, COLORADO

    E-Print Network [OSTI]

    were set as a result of the Federal Water Pollution Control Act Amendments of 1972. The Amendments, #12 Regional Office, Salt Lake City, Utah; Balaji Rajagopalan, Associate Professor, Water Resource Division water quality parameter regulated by federal water quality standards. Federal water quality standards

  10. Fission Product Data Measured at Los Alamos for Fission Spectrum and Thermal Neutrons on {sup 239}Pu, {sup 235}U, {sup 238}U

    SciTech Connect (OSTI)

    Selby, H.D.; Mac Innes, M.R.; Barr, D.W.; Keksis, A.L.; Meade, R.A.; Burns, C.J.; Chadwick, M.B.; Wallstrom, T.C.

    2010-12-15

    We describe measurements of fission product data at Los Alamos that are important for determining the number of fissions that have occurred when neutrons are incident on plutonium and uranium isotopes. The fission-spectrum measurements were made using a fission chamber designed by the National Institute for Standards and Technology (NIST) in the BIG TEN critical assembly, as part of the Inter-laboratory Liquid Metal Fast Breeder Reactor (LMFBR) Reaction Rate (ILRR) collaboration. The thermal measurements were made at Los Alamos' Omega West Reactor. A related set of measurements were made of fission-product ratios (so-called R-values) in neutron environments provided by a number of Los Alamos critical assemblies that range from having average energies causing fission of 400-600 keV (BIG TEN and the outer regions of the Flattop-25 assembly) to higher energies (1.4-1.9 MeV) in the Jezebel, and in the central regions of the Flattop-25 and Flattop-Pu, critical assemblies. From these data we determine ratios of fission product yields in different fuel and neutron environments (Q-values) and fission product yields in fission spectrum neutron environments for {sup 99}Mo, {sup 95}Zr, {sup 137}Cs, {sup 140}Ba, {sup 141,143}Ce, and {sup 147}Nd. Modest incident-energy dependence exists for the {sup 147}Nd fission product yield; this is discussed in the context of models for fission that include thermal and dynamical effects. The fission product data agree with measurements by Maeck and other authors using mass-spectrometry methods, and with the ILRR collaboration results that used gamma spectroscopy for quantifying fission products. We note that the measurements also contradict earlier 1950s historical Los Alamos estimates by {approx}5-7%, most likely owing to self-shielding corrections not made in the early thermal measurements. Our experimental results provide a confirmation of the England-Rider ENDF/B-VI evaluated fission-spectrum fission product yields that were carried over to the ENDF/B-VII.0 library, except for {sup 99}Mo where the present results are about 4%-relative higher for neutrons incident on {sup 239}Pu and {sup 235}U. Additionally, our results illustrate the importance of representing the incident energy dependence of fission product yields over the fast neutron energy range for high-accuracy work, for example the {sup 147}Nd from neutron reactions on plutonium. An upgrade to the ENDF library, for ENDF/B-VII.1, based on these and other data, is described in a companion paper to this work.

  11. Distribution Behavior of U(VI), Pu(IV), Am(III), and Zr(IV) with N,N-Dihexyl Octanamide Under Uranium-Loading Conditions

    SciTech Connect (OSTI)

    Manchanda, V.K.; Ruikar, P.B.; Sriram, S.; Nagar, M.S.; Pathak, P.N.; Gupta, K.K.; Singh, R.K.; Chitnis, R.R.; Dhami, P.S.; Ramanujam, A. [Bhabha Atomic Research Centre (India)

    2001-06-15

    While the tri-n-butyl phosphate (TBP)-based PUREX process has been the workhorse of the nuclear fuel reprocessing industry for the last four and a half decades, a few drawbacks associated with the use of TBP have caused concern to the separation scientists and technologists. These shortcomings may pose a serious challenge particularly during the reprocessing of (a) short cooled thermal reactor fuels, (b) fast reactor fuels with the larger Pu content and significantly higher burn up, and (c) while treating various waste streams for their disposal to the environment. The N,N-dialkyl aliphatic amides have received particular attention as alternate potential extractants for the reprocessing of spent nuclear fuels in view of (a) the innocuous nature of their degradation products, namely, carboxylic acids/amines and (b) the possibility to incinerate the used solvent leading to reduced volume of secondary waste. The physical and chemical properties of these amides are influenced strongly by the nature of alkyl groups. The extractant N,N-dihexyl octanamide (DHOA) was found to be a promising candidate among a large number of extractants studied. Laboratory batch studies as well as mixer settler studies were performed under process conditions with DHOA and compared with those of TBP. DHOA was found to extract Pu(IV) more efficiently than TBP, both at trace-level concentration as well as under uranium loading conditions. In addition, the extraction behavior of Am(III) and Zr(IV) was studied at varying nitric acid concentrations (1 to 6 M). Extraction behavior of uranium at macroconcentrations (9.9 to 157.7 g/l) was carried out at different temperatures, and it was observed that D{sub U} decreased with the increase in U loading as well as with the increase of temperature (in the range 25 to 45 deg. C) and that the two-phase reaction was exothermic in nature. Mixer settler studies on U(VI) revealed that DHOA is similar to TBP during the extraction cycle but better than TBP during the stripping cycle.

  12. Theoretical analyses of (n,xn) reactions on sup 235 U, sup 238 U, sup 237 Np, and sup 239 Pu for ENDF/B-VI

    SciTech Connect (OSTI)

    Young, P.G.; Arthur, E.D.

    1991-01-01

    Theoretical analyses were performed of neutron-induced reactions on {sup 235}U, {sup 238}U, {sup 237}Np, and {sup 239}Pu between 0.01 and 20 MeV in order to calculate neutron emission cross sections and spectra for ENDF/B-VI evaluations. Coupled-channel optical model potentials were obtained for each target nucleus by fitting total, elastic, and inelastic scattering cross section data, as well as low-energy average resonance data. The resulting deformed optical model potentials were used to calculate direct (n,n{prime}) cross sections and transmission coefficients for use in Hauser-Feshbach statistical theory analyses. A fission model with multiple barrier representation, width fluctuation corrections, and preequilibrium corrections were included in the analyses. Direct cross sections for higher-lying vibrational states were calculated using DWBA theory, normalized using B(E{ell}) values determined from (d,d{prime}) and Coulomb excitation data, where available, and from systematics otherwise. Initial fission barrier parameters and transition state density enhancements appropriate to the compound systems involved were obtained from previous analyses, especially fits to charged-particle fission probability data. The parameters for the fission model were adjusted for each target system to obtain optimum agreement with direct (n,f) cross section measurements, taking account of the various multichance fission channels, that is, the different compound systems involved. The results from these analyses were used to calculate most of the neutron (n,n), (n,n{prime}), and (n,xn) cross section data in the ENDF/B/VI evaluations for the above nuclei, and all of the energy-angle correlated spectra. The deformed optical model and fission model parameterizations are described. Comparisons are given between the results of these analyses and the previous ENDF/B-V evaluations as well as with the available experimental data. 14 refs., 3 figs., 1 tab.

  13. Co-operativity among defect sites in AnO2+ and An4O9 (An = U, Np or Pu)

    SciTech Connect (OSTI)

    Andersson, Anders David; Lezama Pacheco, Juan; Uberuaga, Blas P; Conradson, Steven D

    2008-01-01

    Actinide dioxides derived from the AnO{sub 2} fluorite lattice are of high technological relevance due to their application in nuclear reactor fuels. Oxidation of AnO{sub 2} compounds emerges as a central theme in fuel fabrication, reactor operation, long-term storage forms for both spent fuels and surplus weapons materials, and environmental actinide migration. In this paper, we use density functional theory calculations to study the oxidation of uranium, neptunium and plutonium dioxides, AnO{sub 2} (An = U, Np or Pu), in O{sub 2} and O{sub 2}/H{sub 2}O environments. We pay particular attention to the formation of oxygen clusters (co-operativity) in AnO{sub 2+x} and how this phenomenon govern oxidation thermodynamics and the development of ordered An{sub 4}O{sub 9} compounds. The so-called split di-interstitial, which is composed of two nearest neighbor octahedral oxygen interstitials that are distorted in such a way that they dislocate one regular fluorite lattice oxygen ion to form a cluster of triangular geometry, is predicted to be the fundamental building block of the most stable cluster configurations. We also identify how the formation of oxygen defect clusters and the degree of oxidation in AnO{sub 2+x} are both governed by the characer of the An-5f to excess O-2p charger transfer, i.e. the charge transfer to the O-2p orbitals of the interstitial-like (+x) ions, and the ability of the excess O-2p orbitals to hybridize with regular fluorite lattice ions.

  14. The Political Rebellion of Carey McWilliams

    E-Print Network [OSTI]

    Critser, Greg

    1983-01-01

    May in Bruno Lasky, "Feudalism in California," The Survey 42to one reminiscent of feudalism in the middle ages." ^^ j^ a

  15. Microsoft Word - Document2

    Broader source: Energy.gov (indexed) [DOE]

    The following individuals were present or on the telephone: Jeremy Dommu, DOE Dan Cohen, DOE Celia Sher, DOE Pierre Delforge, NRDC Benjamin Longstreth, NRDC Andrew deLaski,...

  16. Plutonium stabilization and handling (PuSH)

    SciTech Connect (OSTI)

    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.

  17. Cs and 239,240 Pu concentration

    E-Print Network [OSTI]

    Buesseler, Ken

    . Noshkinh , Shigeki Shimai , Orihiko Togawaa,1 a International Atomic Energy Agency, Marine Environment, Denmark c Woods Hole Oceanographic Institution, Woods Hole, MA 02543, USA d ENEA, Marine Environment, Seoul, Republic of Korea g Federal Maritime & Hydrographic Agency, Marine Chemistry Laboratory, Hamburg

  18. NR Pu SEIS Advisory 07272012_Clean

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration wouldMass map shines light on771/6/14 Contact: JanetSite661.

  19. Examining 239Pu and 240Pu Nuclear Resonance Fluorescence Measurements on Spent Fuel for Nuclear Safeguards

    E-Print Network [OSTI]

    Quiter, Brian

    2013-01-01

    10- 01096) Journal of Nuclear Technology, p. 150, Vol. 175,linac and laser technologies for nuclear photonics gamma-rayNuclear resonance fluorescence (NRF) has been identified as a technology

  20. Microsoft Word - Ex Parte Memo re October 28, 2014 Meeting on...

    Energy Savers [EERE]

    or on the telephone: John Cymbalsky, DOE Dan Cohen, DOE Andrew deLaski, ASAP Wade Smith, AMCA International Marc Bublitz, New York Blower Company Tom Catania, University of...

  1. Encounter with Zoology

    E-Print Network [OSTI]

    Macfarlane, Alan

    2014-12-12

    Research and possibly Wellcome gave money for the refurbishment of laboratories for Gurdon and Lasky and the thing 24 took off; later had the opportunity to appoint Mike Bate also a young, distinguished, developmental biologist; had this extraordinary...

  2. Multiscale Speciation of U and Pu at Chernobyl, Hanford, Los...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    initial step in U paragenesis is oxidation so that subsequent alteration phases are uranyl compounds, the absence of U(VI) may be because of the high temperature and...

  3. Pu#ng Groundwater into Agro-IBIS

    E-Print Network [OSTI]

    below the top of the capillary fringe to represent groundwater · This modificaCviCes of · TranspiraCon to depth to water table · NPP to depth to water table · Next water table is shallow · Regional climate directly interacts with groundwater

  4. Savannah River Site: Plutonium Preparation Project (PuPP) at...

    Office of Environmental Management (EM)

    Site October 2008 Dr. David S. Kosson, Vanderbilt University Dr. David R. Gallay, Logistics Management Institute Dr. R. Bruce Mathews, Consultant Mr. David Nulton, National...

  5. Ceramicrete stabilization of U-and Pu-bearing materials

    DOE Patents [OSTI]

    Wagh, Arun S. (Naperville, IL); Maloney, M. David (Evergreen, CO); Thompson, Gary H. (Thornton, CO)

    2007-11-13

    A method of stabilizing nuclear material is disclosed. Oxides or halides of actinides and/or transuranics (TRUs) and/or hydrocarbons and/or acids contaminated with actinides and/or TRUs are treated by adjusting the pH of the nuclear material to not less than about 5 and adding sufficient MgO to convert fluorides present to MgF.sub.2; alumina is added in an amount sufficient to absorb substantially all hydrocarbon liquid present, after which a binder including MgO and KH.sub.2PO.sub.4 is added to the treated nuclear material to form a slurry. Additional MgO may be added. A crystalline radioactive material is also disclosed having a binder of the reaction product of calcined MgO and KH.sub.2PO.sub.4 and a radioactive material of the oxides and/or halides of actinides and/or transuranics (TRUs). Acids contaminated with actinides and/or TRUs, and/or actinides and/or TRUs with or without oils and/or greases may be encapsulated and stabilized by the binder.

  6. Curriculum Vitae of Dr. Chang-Pu Sun Personal Data

    E-Print Network [OSTI]

    Sun, Chang-Pu

    on the artificial photosynthesis with quantum effects. For fundamental quantum physics, I believe that the origin

  7. Nuclear magnetic resonance offers new insights into Pu 239

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration wouldMass map shinesSolarNewsusceptometer under pressureNavy TurnsNuclear

  8. Elasticity of Pu -a window into fundamental understanding and aging

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfate Reducing(Journal Article) | SciTech(Journal Article) | SciTech(JournalSciTechElastic Moduli

  9. Elasticity of Pu -a window into fundamental understanding and aging

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfate Reducing(Journal Article) | SciTech(Journal Article) | SciTech(JournalSciTechElastic

  10. Report on the Feasibility of Pu Photoelectron Spectroscopy with Microscopic

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfateSciTech ConnectSpeedingConnect(Conference)Factory: Linear vs. Circular'

  11. Report on the Feasibility of Pu Photoelectron Spectroscopy with Microscopic

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfateSciTech ConnectSpeedingConnect(Conference)Factory: Linear vs. Circular'and Nanoscopic

  12. Status of Pu-239 Evaluations (Conference) | SciTech Connect

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfateSciTechtail. (Conference)Feedback System in thewitnessChiralTechnicalchange.StructuresStatus of

  13. Status of Pu-239 Evaluations (Conference) | SciTech Connect

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfateSciTechtail. (Conference)Feedback System in thewitnessChiralTechnicalchange.StructuresStatus

  14. The Evolution in Pu Nanocluster Electronic Structure: from Atomicity to

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfateSciTechtail. (Conference)FeedbackProperties of Graphene (Journal Article)(Conference) |

  15. The Evolution in Pu Nanocluster Electronic Structure: from Atomicity to

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfateSciTechtail. (Conference)FeedbackProperties of Graphene (Journal Article)(Conference) |Three

  16. NR Pu SEIS Advisory 07152010 _final_.doc

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity ofkandz-cm11 Outreach Home Room NewsInformationJessework usesof EnergyY-12 NationalNO FEAR Act Notice NONPSRS: Jim Giusti,

  17. Configuring PuTTY for use with ssh.gfdl.noaa.gov 1. Start PuTTY

    E-Print Network [OSTI]

    forwarding". Enter "localhost:0" in the X display location "textbox". 9. Click on the "Tunnels" in the sub other hosts". Click the "Add" button. #12;5 The Tunnels screen should now look like the image: Remember: "ssh.gfdl.noaa.gov" is only a gateway. ssh.gfdl.noaa.gov does not have tools to enable you

  18. Separating expansion from contraction: generalized TOV condition, LTB models with pressure and CDM

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    , we adopt the Generalised Painlevé-Gullstrand (hereafter GPG) formalism used in Lasky & Lun [6], which TO LTB MODELS IN GPG SYSTEM We consider a spherically symmetric Generalised Lemaître-Tolman-Bondi metric to include pressure. Performing an ADM 3+1 splitting in the GPG coordinates [6] , the metric reads ds2 = -(t

  19. 2001 Participating Schools Abraham Wing School

    E-Print Network [OSTI]

    School of Humanities Teacher: Ms. Vivian Hansen Students: Catherine Calsolaro Lusonta Harvin Shaharazod, Mrs. Miller and Mrs. Stokes Students: Jordan Adderly Mariah Brown Antonio Davis Raven Dixon Jabril Teachers: Mr. Gerald Germano, Ms. Karen Lasky and Mrs. Joy G. Sokero Students: Miranda Allen Cassie Card

  20. Rational Ligand Design for U(VI) and Pu(IV)

    E-Print Network [OSTI]

    Szigethy, Geza

    2010-01-01

    and Related Methods of Nuclear Waste Management; Choppin, G.and Related Methods of Nuclear Waste Management; Choppin, G.

  1. SynthESizing uMD-lED CEntER PuRSuES

    E-Print Network [OSTI]

    Hill, Wendell T.

    . The Socio-Environmental Synthesis Center, known as SeSynC, uses data and knowledge gleaned from biologists SeSynC looks to answer urgent questions on ecosystem management while educating the public Hultman, an expert on nuclear energy and low-carbon technologies, who is assistant director of the Joint

  2. Rational Ligand Design for U(VI) and Pu(IV)

    E-Print Network [OSTI]

    Szigethy, Geza

    2010-01-01

    Design for the Uranyl Cation, UO 22+ ………………………. ……………….15tripodal ligands for uranyl chelation …………………….19 Figurestudies with the uranyl cation ………………………………………………. 36 Figure

  3. Materials Data on PuCo3 (SG:166) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  4. Materials Data on PuCo3 (SG:166) by Materials Project

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Kristin Persson

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  5. Oakwood crown closure estimation by unmixing Landsat TM data R. PU*, B. XU and P. GONG

    E-Print Network [OSTI]

    Silver, Whendee

    ) algorithm, we estimated oakwood crown closure from a Landsat Thematic Mapper (TM) image of Tulare County

  6. Rational Ligand Design for U(VI) and Pu(IV)

    E-Print Network [OSTI]

    Szigethy, Geza

    2010-01-01

    V.4.024; Siemens Industrial Automation, Inc, Madison, WI,V.4.024; Siemens Industrial Automation, Inc, Madison, WI,

  7. Materials Data on Pu(SiPd)2 (SG:139) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  8. Materials Data on Pu(CoSi)2 (SG:139) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  9. Materials Data on Pu(SiRh)2 (SG:139) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  10. PU AST558, 4/25/05 ST Science & Fusion Energy Martin Peng

    E-Print Network [OSTI]

    plasma particles and waves interact? · How do hot plasmas interact with walls? · How to supply magnetic PPPL Spherical Tokamak Plasma Science & Fusion Energy Development Supported by Columbia U Comp Tokamak (ST) Offers Rich Plasma Science Opportunities and High Fusion Energy Potential · What is ST

  11. Type B Accident Investigation on the August 5, 2003, Pu-238 Multiple...

    Energy Savers [EERE]

    Board concluded that the direct cause of the accident was the release of airborne contamination from a degraded package that contained cellulose material and plutonium-238...

  12. Reaction kinetics for the high temperature oxidation of Pu--1wt%Ga in water vapor

    SciTech Connect (OSTI)

    Stakebake, J L; Saba, M A

    1988-01-01

    Oxidation of plutonium metal is greatly accelerated by the presence of water vapor. The magnitude of the effect of water vapor on oxidation kinetics is determined by temperature, water concentration, and oxygen concentration. Most of the previous work has been directed toward evaluating the effect of moisture on the atmospheric oxidation of plutonium. Work on the isolation and characterization of the water reaction with plutonium has been very limited. The present work was undertaken to determine the kinetics of the plutonium--water reaction over a wide range of temperature and pressure. Reaction kinetics were measured using a vacuum microbalance system. The temperature range investigated was 100--500/degree/C. The effect of water vapor pressure on reaction kinetics was determined at 300/degree/C by varying the water pressure from 0.1 to 15 Torr. 2 figs.

  13. Materials Data on Pu(SiNi)2 (SG:139) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  14. Materials Data on PuBi (SG:225) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  15. Coprocessed nuclear fuels containing (U, Pu) values as oxides, carbides or carbonitrides

    DOE Patents [OSTI]

    Lloyd, M.H.

    1981-01-09

    Method for direct coprocessing of nuclear fuels derived from a product stream of fuels reprocessing facility containing uranium, plutonium, and fission product values comprising nitrate stabilization of said stream vacuum concentration to remove water and nitrates, neutralization to form an acid deficient feed solution for the internal gelation mode of sol-gel technology, green spherule formation, recovery and treatment for loading into a fuel element by vibra packed or pellet formation technologies.

  16. Coprocessed nuclear fuels containing (U, Pu) values as oxides, carbides or carbonitrides

    DOE Patents [OSTI]

    Lloyd, Milton H. (Oak Ridge, TN)

    1983-01-01

    Method for direct coprocessing of nuclear fuels derived from a product stream of a fuels reprocessing facility containing uranium, plutonium, and fission product values comprising nitrate stabilization of said stream vacuum concentration to remove water and nitrates, neutralization to form an acid deficient feed solution for the internal gelation mode of sol-gel technology, green spherule formation, recovery and treatment for loading into a fuel element by vibra packed or pellet formation technologies.

  17. Microscopic Calculation of 240Pu Scission with a Finite-Range...

    Office of Scientific and Technical Information (OSTI)

    CA Sponsoring Org: USDOE Country of Publication: United States Language: English Subject: 73 NUCLEAR PHYSICS AND RADIATION PHYSICS; ALGORITHMS; BENCHMARKS; FISSION; SENSITIVITY...

  18. Nanopropeller arrays of zinc oxide Pu Xian Gao and Zhong L. Wanga)

    E-Print Network [OSTI]

    Wang, Zhong L.

    , optoelectronic, photovoltaic devices, and sensors.1­5 Quasi-one-dimensional nanostructures of Zn of the nanopropellers remain their sixfold arrays of parallel nanor- ibbon blades around the central nanowire Fig. 1 b

  19. Materials Data on PuAs (SG:225) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  20. Materials Data on PuOF (SG:216) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  1. Materials Data on PuAl3 (SG:194) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  2. Materials Data on PuRh3 (SG:221) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  3. Materials Data on Pu2Co (SG:189) by Materials Project

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  4. Materials Data on PuGe2 (SG:141) by Materials Project

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  5. Theory of nodal s±-wave pairing symmetry in the Pu-based 115 superconductor family

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Das, Tanmoy; Zhu, Jian -Xin; Graf, Matthias J.

    2015-02-27

    The spin-fluctuation mechanism of superconductivity usually results in the presence of gapless or nodal quasiparticle states in the excitation spectrum. Nodal quasiparticle states are well established in copper-oxide, and heavy-fermion superconductors, but not in iron-based superconductors. Here, we study the pairing symmetry and mechanism of a new class of plutonium-based high-Tc superconductors and predict the presence of a nodal s?? wave pairing symmetry in this family. Starting from a density-functional theory (DFT) based electronic structure calculation we predict several three-dimensional (3D) Fermi surfaces in this 115 superconductor family. We identify the dominant Fermi surface “hot-spots” in the inter-band scattering channel,more »which are aligned along the wavevector Q = (?, ?, ?), where degeneracy could induce sign-reversal of the pairing symmetry. Our calculation demonstrates that the s?? wave pairing strength is stronger than the previously thought d-wave pairing; and more importantly, this pairing state allows for the existence of nodal quasiparticles. Finally, we predict the shape of the momentum- and energy-dependent magnetic resonance spectrum for the identification of this pairing symmetry.« less

  6. Materials Data on Pu3Al (SG:123) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  7. Summary of Pu?u ?O?o - Kupaianaha Eruption, Kilauea Volcano...

    Open Energy Info (EERE)

    Survey, 2012 DOI Not Provided Check for DOI availability: http:crossref.org Online Internet link for Summary of Puu Oo - Kupaianaha Eruption, Kilauea Volcano, Hawaii...

  8. Spin-orbit holds the heavyweight title for Pu and Am: Exchange regains it for Cm

    SciTech Connect (OSTI)

    Moore, K; der Laan, G v; Soderlind, P

    2008-01-10

    The conclusions of this paper are: (1) The 5f electrons in Cm are near an LS coupling scheme. (2) This coupling scheme allows for a large spin polarization of the 5f electrons, which in turn stabilizes the Cm III crystal structure. (3) Results for Cm show us the recipe for magnetic stabilization of the crystal structure of metals: (A) The metal must be near the itinerant-localized transition where multiple crystal structures have close energies; (B) The metal is just on the magnetic side of the transition; and (C) There must be a magnetic moment large enough to overcome the energy difference between crystal structures, thus dictating the atomic geometry. (4) These results solidify our understanding of magnetically-stabilized metals, showing us where to look for engineered materials with magnetic applications.

  9. Materials Data on PuIn (SG:123) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  10. Materials Data on PuIn3 (SG:221) by Materials Project

    SciTech Connect (OSTI)

    Kristin Persson

    2014-11-02

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  11. Materials Data on PuNi2 (SG:227) by Materials Project

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Kristin Persson

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  12. Materials Data on PuGe2 (SG:141) by Materials Project

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Kristin Persson

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  13. Materials Data on Pu2Co (SG:189) by Materials Project

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Kristin Persson

    Computed materials data using density functional theory calculations. These calculations determine the electronic structure of bulk materials by solving approximations to the Schrodinger equation. For more information, see https://materialsproject.org/docs/calculations

  14. New Superheavy Element Isotopes: 242Pu(48Ca,5n)285114

    E-Print Network [OSTI]

    Ellison, Paul A

    2010-01-01

    ? decay of four daughter nuclides, 281 Cn, 277 Ds, 273 Hs,hanced stability consisting of nuclides produced by 48 Capublished half- life for the nuclide [1], and (iii) SF was

  15. Evaluation of Los Alamos National Laboratory (LANL) PU238 Waste Management Practices

    Broader source: Energy.gov [DOE]

    Supporting Technical Document for the Radiological Release Accident Investigation Report (Phase II Report)

  16. Quantitative NDA Measurements of Advanced Reprocessing Product Materials Containing U, NP, PU, and AM 

    E-Print Network [OSTI]

    Goddard, Braden

    2013-04-05

    of this first principle technique have been identified: (1) quantitative measurement of uranium, neptunium, plutonium, and americium materials; (2) quantitative measurement of mixed oxide (MOX) materials; (3) quantitative measurement of uranium materials; and (4...

  17. Rational Ligand Design for U(VI) and Pu(IV)

    E-Print Network [OSTI]

    Szigethy, Geza

    2010-01-01

    in turn, requires very specific reprocessing and separation7 Ci, t ½ = 30.0 yr). Reprocessing this waste is a complexefficient storage and/or reprocessing applicaitons. 8

  18. Llr. Norgnn of the St. Louis office tolepbonod Dr. ;PuAuff mcently

    Office of Legacy Management (LM)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefield Municipal Gas &SCE-SessionsSouth DakotaRobbins and MyersHr. Anthony V. Andolina:I 1 '\Ll 1

  19. Table A1. Total First Use (formerly Primary Consumption) of Energy for All Pu

    U.S. Energy Information Administration (EIA) Indexed Site

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: AlternativeMonthly","10/2015"Monthly","10/2015" ,"Release7CubicthroughtheSeptember 24,4,630.22 Consumption Ratios of4796 Table1

  20. Table A1. Total First Use (formerly Primary Consumption) of Energy for All Pu

    U.S. Energy Information Administration (EIA) Indexed Site

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: AlternativeMonthly","10/2015"Monthly","10/2015" ,"Release7CubicthroughtheSeptember 24,4,630.22 Consumption Ratios of4796

  1. 6th US-Russian Pu Science Workshop Lawrence Livermore National Laboratory

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity ofkandz-cm11 Outreach Home RoomPreservationBio-InspiredAtmosphericdevicesPPONeApril351APPLICATION OF kVProposed

  2. Shenzhen Prosunpro PengSangPu Solar Industrial Products Corporation | Open

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on QA:QA J-E-1 SECTION J APPENDIX ECoop Inc JumpHeter Battery Technology Co LtdOhio: EnergyIndustryCo Ltd Jump

  3. Summary of Pu u O o - Kupaianaha Eruption, Kilauea Volcano, Hawaii | Open

    Open Energy Info (EERE)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on QA:QA J-E-1 SECTION JEnvironmental Jump to:EA EIS ReportEurope

  4. Discovery of Pu-based superconductors and relation to other classes of

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefield MunicipalTechnical Report: Achievements ofCOMPOSITION OFProcess Laboratory (Technical Report)

  5. (U) CIELO: Status of 239Pu Evaluation (Conference) | SciTech Connect

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefield MunicipalTechnicalInformation4563 LLNL Small-scale Friction Sensitivityv b,Monitoringin thein

  6. (U) CIELO: Status of 239Pu Evaluation (Conference) | SciTech Connect

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefield MunicipalTechnicalInformation4563 LLNL Small-scale Friction Sensitivityv b,Monitoringin thein(U)

  7. Energy Dependence of Fission Product Yields for 239Pu, 235U, and 238U

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfate Reducing(Journal Article) | SciTech(Journal Article)atDiagnosticsFacility (Journal Article)

  8. Energy Dependence of Fission Product Yields for 239Pu, 235U, and 238U

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfate Reducing(Journal Article) | SciTech(Journal Article)atDiagnosticsFacility (Journal

  9. Microscopic Calculation of 240Pu Scission with a Finite-Range Effective

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfate Reducing(JournalspectroscopyReport) |(Patent) |monitoring.(Patent) |methodForce (Journal

  10. Microscopic Calculation of 240Pu Scission with a Finite-Range Effective

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfate Reducing(JournalspectroscopyReport) |(Patent) |monitoring.(Patent) |methodForce (JournalForce

  11. Microscopic Calculation of Fission Fragment Energies for the 239Pu(nth,f)

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfate Reducing(JournalspectroscopyReport) |(Patent) |monitoring.(Patent) |methodForce

  12. Microscopic Calculation of Fission Fragment Energies for the 239Pu(nth,f)

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfate Reducing(JournalspectroscopyReport) |(Patent) |monitoring.(Patent) |methodForceReaction

  13. V-213: PuTTY SSH Handshake Integer Overflow Vulnerabilities | Department of

    Broader source: Energy.gov (indexed) [DOE]

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of Natural GasAdjustmentsShirleyEnergyThe U.S.Lacledeutilities. The EconomicsVulnerabilities | DepartmentEnergy

  14. Savannah River Site: Plutonium Preparation Project (PuPP) at Savannah River

    Energy Savers [EERE]

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on DeliciousMathematicsEnergyInterestedReplacement-2-AA-1 SECTION JSTEM-ing theSummarySavannah River Site SavannahSite

  15. Multiscale Speciation of U and Pu at Chernobyl, Hanford, Los Alamos,

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity ofkandz-cm11 Outreach Home Room NewsInformationJessework usesof Energy Moving Forward to AddressMcGuire AFB, Mayak, and

  16. Microsoft PowerPoint - Draft HAB Pu presentation CJK 040412.pptx [Read-Only]

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantityBonneville Power Administration wouldMass map shines light on darkMicroorganisms toPalladium wavyfamily Distribution with 3D 4 5

  17. Suburban Place? Constructing Place in Overland Park, Kansas

    E-Print Network [OSTI]

    Carey, Daniel

    2008-08-21

    childhood, like ?Return of the Jedi? in the Art Moderne-style Glenwood Theatre, and going with my father to Red?s barbershop in downtown Overland Park for the cheapest haircut in town. In addition, I recall working at the ?Ken-Taco-Hut? (the nickname...

  18. **The specific contact information included in this document are current as of 11/18/2011. AppendixB:LargeNebraskaSchoolDistricts

    E-Print Network [OSTI]

    Farritor, Shane

    Schools High Schools Fire Ridge Elkhorn Middle School Elkhorn High School Hillrise Elk Ridge Middle School Emerson Glenwood Kenwood Meadowlark Northeast Park Riverdale Stone Windy Hills #12;**The specific contact Fredstrom Hartley Hill Holmes Humann Huntington Kahoa Kooser Lakeview Maxey McPhee Meadow Lane Morley

  19. 18 Department of Geology and Geophysics University of Wisconsin-Madison Ordovician in Wisconsin Theses

    E-Print Network [OSTI]

    Johnson, Clark M.

    Sandstones in central Wisconsin, Ph.D., 1952. Choi, Yong Seok: Stratigraphy and sedimentology of the Middle and sedimentology of the Middle to Upper Ordovician Ancell and Sinnipee groups, Wisconsin, Ph.D., 1998. Deninger of underground waters in the St. Peter Sandstone, M.A., 1927. Long, John Douglas: Sedimentology of the Glenwood

  20. Topological Analysis of Void Spaces in Tungstate Frameworks: Assessing Storage Properties for the Environmentally Important Guest Molecules and Ions: CO_2, UO_2, PuO_2, U, Pu, Sr^2+, Cs+, CH_4, and H_2

    E-Print Network [OSTI]

    Cole, Jacqueline Manina; Cramer, Alisha J.; Zeidler, Anita

    2015-07-15

    appropriate. In the ongoing search for usable materials, data mining of structure databases can provide a useful tool to identify potential candidates for the applications in hand. For example, a study on Li+ migration maps26 examined the structure... products found in nuclear waste. Waste from nuclear facilities, in the form of spent nuclear fuel, is found predominantly in the form of uranium or plutonium oxides.28 Furthermore, current efforts, especially among tungstates, are largely focused...

  1. Modeling Constituent Redistribution in U-Pu-Zr Metallic Fuel Using the Advanced Fuel Performance Code BISON

    SciTech Connect (OSTI)

    Douglas Porter; Steve Hayes; Various

    2014-06-01

    The Advanced Fuels Campaign (AFC) metallic fuels currently being tested have higher zirconium and plutonium concentrations than those tested in the past in EBR reactors. Current metal fuel performance codes have limitations and deficiencies in predicting AFC fuel performance, particularly in the modeling of constituent distribution. No fully validated code exists due to sparse data and unknown modeling parameters. Our primary objective is to develop an initial analysis tool by incorporating state-of-the-art knowledge, constitutive models and properties of AFC metal fuels into the MOOSE/BISON (1) framework in order to analyze AFC metallic fuel tests.

  2. Effect of 1-hydroxyethane-1,1-diphosphonic acid (HEDPA) on Partitioning of Np and Pu to Synthetic Boehmite

    E-Print Network [OSTI]

    Powell, Brian A.

    2010-01-01

    of plutonium IV and V on goethite. Geochim. Cosmo. Acta,reduction on synthetic goethite (?-FeOOH) and hematite (?-Fe

  3. Fusion med dPu Pesticider gteskabskonomen Program For eFter-og videreuddannelse aarHus universitet

    E-Print Network [OSTI]

    Uggerhøj, Ulrik I.

    forbindelse 18 Danmark i det lune hjørne 21 Ingen panik, men seriøs handling 24 Flere planter og dyr i- dannelse vælger at rejse ud. I dag er der ingen grænser for hjernernes fri bevægelighed, medmin- dre

  4. Study of Pu consumption in Advanced Light Water Reactors. Evaluation of GE Advanced Boiling Water Reactor plants

    SciTech Connect (OSTI)

    Not Available

    1993-05-13

    Timely disposal of the weapons plutonium is of paramount importance to permanently safeguarding this material. GE`s 1300 MWe Advanced Boiling Water Reactor (ABWR) has been designed to utilize fill] core loading of mixed uranium-plutonium oxide fuel. Because of its large core size, a single ABWR reactor is capable of disposing 100 metric tons of plutonium within 15 years of project inception in the spiking mode. The same amount of material could be disposed of in 25 years after the start of the project as spent fuel, again using a single reactor, while operating at 75 percent capacity factor. In either case, the design permits reuse of the stored spent fuel assemblies for electrical energy generation for the remaining life of the plant for another 40 years. Up to 40 percent of the initial plutonium can also be completely destroyed using ABWRS, without reprocessing, either by utilizing six ABWRs over 25 years or by expanding the disposition time to 60 years, the design life of the plants and using two ABWRS. More complete destruction would require the development and testing of a plutonium-base fuel with a non-fertile matrix for an ABWR or use of an Advanced Liquid Metal Reactor (ALMR). The ABWR, in addition, is fully capable of meeting the tritium target production goals with already developed target technology.

  5. CFD analyse av mikrofluidisk Lab-on-a-Chip komponent E&M/PuP/I&IKT

    E-Print Network [OSTI]

    Müller,Bernhard

    systemer for kjemisk, biologisk og medisinsk analyse har ført til konsepter som bioMEMS (bio-micro-electro-mechanical systems), microTAS (micro total analysis systems), og Lab-On-a-Chip. Ideen er å integrere et helt

  6. Fast, Optimized Sun RPC Using Automatic Program Specialization Gilles Muller, Renaud Marlet, Calton Pu and Ashvin Goel

    E-Print Network [OSTI]

    Goel, Ashvin

    Fast, Optimized Sun RPC Using Automatic Program Specialization Gilles Muller, Renaud Marlet, Calton automatic optimization of an existing, commercial RPC implementation, namely the Sun RPC. The optimized Sun the original Sun RPC. Close examination of the specialized code does not reveal further optimization

  7. The Utilization of Spin Polarized Photoelectron Spectroscopy as a Probe of Electron Correlation with an Ultimate Goal of Pu

    E-Print Network [OSTI]

    Tobin, James

    2009-01-01

    or Lawrence Livermore National Security, LLC, and shall notby Lawrence Livermore National Security, LLC, for the U.S.Lawrence Livermore National Security, LLC, nor any of their

  8. JOINT STUDY OF IMPROVED SAFEGUARDS METHODOLOGY USING NO-NOTICE RANDOMIZED INSPECTION AT JNC'S Pu HANDLING FACILITIES

    SciTech Connect (OSTI)

    LU,M.S.; SANBORN,J.B.

    2000-04-01

    After the Iraq war, the International Atomic Energy Agency (IAEA) 93+2 Program was developed to strengthen and improve the cost-effectiveness of the existing safeguards system. In particular, the Program aims to enhance the IAEA ability to detect undeclared nuclear activities and materials. The IAEA 93+2 Program includes: (1) Increased access to information and its effective use; (2) Increased physical access; (3) Optimum use of the existing system. The measures considered are divided in two parts: measures in Part 1 are those, which may be implemented within the existing IAEA authority; Part 2 measures require complementary legal authority, in the form of an additional Protocol, INFCIRC/540. A description of the status of its implementation can be found in ``Implementation of the Additional Protocol'' (Cooley, 1999). In particular, increased physical access includes access beyond locations requiring additional authorities derived from the INFCIRC/540 and no-notice randomized inspections. No-notice randomized inspections could enhance the inspection effectiveness and efficiency by increasing the coverage of the material involved, providing better confirmation of the operational status of the facilities and higher degree of confidence that no undeclared activities or materials existed at the facilities--including the detection of possible measures to conceal diversions.

  9. Effect of 1-hydroxyethane-1,1-diphosphonic acid (HEDPA) on Partitioning of Np and Pu to Synthetic Boehmite

    E-Print Network [OSTI]

    Powell, Brian A.

    2010-01-01

    Dissolution of Waste Tank Sludge Surrogates. Separationin Hanford Waste Tank Sludge Simulants. J. Nucl. Sci.during experimental sludge washing of bismuth phosphate,

  10. THERMAL EVALUATION OF THE CONCEPTUAL DHLW DISPOSAL CONTAINER LOADED WITH PU/CS GREENFIELD GLASS (SCPB: N/A)

    SciTech Connect (OSTI)

    T.L. Lotz

    1995-11-13

    This analysis is prepared by the Mined Geologic Disposal System (MGDS) Waste Package Development Department (WPDD) as specified in the Waste Package Implementation Plan (pp. 4-8,4-11,4-24,5-1, and 5-13; Ref. 5.10) and Waste Package Plan (pp. 3-15,3-17, and 3-24; Ref. 5.9). The design data request addressed herein is: Characterize the conceptual Defense High Level Waste (DHLW) Disposal Container design to show that the design is feasible for use in the MGDS environment when loaded with a plutonium/cesium greenfield glass waste form. The purpose of this analysis is to respond to a concern that the long-term disposal thermal issues for the conceptual DHLW disposal container design do not preclude compatibility with the MGDS if it is loaded with alternate waste forms. The objective of this analysis is to provide thermal parameter information for the conceptual DHLW disposal container design loaded with an alternative waste form containing a plutonium/cesium mixture under nominal MGDS repository conditions. The results are intended to show that the design loaded with this alternative waste form has a reasonable chance to meet the MGDS design requirements for normal MGDS operation and to provide the required guidance to determining the major design issues for future design efforts. Future design efforts will focus on specific DHLW vendor designs and improved waste form data when they become available.

  11. Summary of EXAFS results on Cd-doped PuRhIn5 (Technical Report) | SciTech

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfateSciTechtail. (Conference)Feedback System inStatus ofSmall GTPasesmirroranΦ¹²Special

  12. Summary of EXAFS results on Cd-doped PuRhIn5 (Technical Report) | SciTech

    Office of Scientific and Technical Information (OSTI)

    AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Homesum_a_epg0_fpd_mmcf_m.xls" ,"Available from WebQuantity of NaturalDukeWakefieldSulfateSciTechtail. (Conference)Feedback System inStatus ofSmall GTPasesmirroranΦ¹²SpecialConnect

  13. Environmental assessment operation of the HB-Line facility and frame waste recovery process for production of Pu-238 oxide at the Savannah River Site

    SciTech Connect (OSTI)

    1995-04-01

    The Department of Energy (DOE) has prepared an environmental assessment (EA), DOE/EA-0948, addressing future operations of the HB-Line facility and the Frame Waste Recovery process at the Savannah River Site (SRS), near Aiken, South Carolina. Based on the analyses in the EA, DOE has determined that the proposed action is not a major Federal action significantly affecting the quality of the human environment within the meaning of the National Environmental Policy Act (NEPA) of 1969. Therefore, DOE has concluded that, the preparation of an environmental impact statement is not required, and is issuing this Finding of No Significant Impact.

  14. A Brief Review of Past INL Work Assessing Radionuclide Content in TMI-2 Melted Fuel Debris: The Use of 144Ce as a Surrogate for Pu Accountancy

    SciTech Connect (OSTI)

    D. L. Chichester; S. J. Thompson

    2013-09-01

    This report serves as a literature review of prior work performed at Idaho National Laboratory, and its predecessor organizations Idaho National Engineering Laboratory (INEL) and Idaho National Engineering and Environmental Laboratory (INEEL), studying radionuclide partitioning within the melted fuel debris of the reactor of the Three Mile Island 2 (TMI-2) nuclear power plant. The purpose of this review is to document prior published work that provides supporting evidence of the utility of using 144Ce as a surrogate for plutonium within melted fuel debris. When the TMI-2 accident occurred no quantitative nondestructive analysis (NDA) techniques existed that could assay plutonium in the unconventional wastes from the reactor. However, unpublished work performed at INL by D. W. Akers in the late 1980s through the 1990s demonstrated that passive gamma-ray spectrometry of 144Ce could potentially be used to develop a semi-quantitative correlation for estimating plutonium content in these materials. The fate and transport of radioisotopes in fuel from different regions of the core, including uranium, fission products, and actinides, appear to be well characterized based on the maximum temperature reached by fuel in different parts of the core and the melting point, boiling point, and volatility of those radioisotopes. Also, the chemical interactions between fuel, fuel cladding, control elements, and core structural components appears to have played a large role in determining when and how fuel relocation occurred in the core; perhaps the most important of these reaction appears to be related to the formation of mixed-material alloys, eutectics, in the fuel cladding. Because of its high melting point, low volatility, and similar chemical behavior to plutonium, the element cerium appears to have behaved similarly to plutonium during the evolution of the TMI-2 accident. Anecdotal evidence extrapolated from open-source literature strengthens this logical feasibility for using cerium, which is rather easy to analyze using passive nondestructive analysis gamma-ray spectrometry, as a surrogate for plutonium in the final analysis of TMI-2 melted fuel debris. The generation of this report is motivated by the need to perform nuclear material accountancy measurements on the melted fuel debris that will be excavated from the damaged nuclear reactors at the Fukushima Daiichi nuclear power plant in Japan, which were destroyed by the Tohoku earthquake and tsunami on March 11, 2011. Lessons may be taken from prior U.S. work related to the study of the TMI-2 core debris to support the development of new assay methods for use at Fukushima Daiichi. While significant differences exist between the two reactor systems (pressurized water reactor (TMI-2) versus boiling water reactor (FD), fresh water post-accident cooing (TMI-2) versus salt water (FD), maintained containment (TMI-2) versus loss of containment (FD)) there remain sufficient similarities to motivate these comparisons.

  15. I. Nuclear Production Reaction and Chemical Isolation Procedure for 240Am II. New Superheavy Element Isotopes: 242Pu(48Ca,5n)285-114

    E-Print Network [OSTI]

    Ellison, Paul Andrew

    2011-01-01

    48 Ca, 5n) 285 114 nuclear reaction cross section. . . . .240 Am(n, f ) cross section 1.4 Nuclear properties of 2401.5 Nuclear reactions for the production of 240 Am . 2

  16. I. Nuclear Production Reaction and Chemical Isolation Procedure for 240Am II. New Superheavy Element Isotopes: 242Pu(48Ca,5n)285-114

    E-Print Network [OSTI]

    Ellison, Paul Andrew

    2011-01-01

    of superheavy nuclei in cold fusion reactions. Phys. Rev. C,transfermium elements in cold fusion reactions. Phys. Rev.have been deemed “cold fusion” reactions because of the low

  17. Cleanup levels for Am-241, Pu-239, U-234, U-235 & U-238 in soils at the Rocky Flats Environmental Technology Site

    SciTech Connect (OSTI)

    Roberts, R.; Colby, B.; Brooks, L.; Slaten, S.

    1997-07-03

    This presentation briefly outlines a cleanup program at a Rocky Flats site through viewgraphs and an executive summary. Exposure pathway analyses to be performed are identified, and decontamination levels are listed for open space and office worker exposure areas. The executive summary very briefly describes the technical approach, RESRAD computer code to be used for analyses, recommendations for exposure levels, and application of action levels to multiple radionuclide contamination. Determination of action levels for surface and subsurface soils, based on radiation doses, is discussed. 1 tab.

  18. Design and Nuclear-Safety Related Simulations of Bare-Pellet Test Irradiations for the Production of Pu-238 in the High Flux Isotope Reactor using COMSOL

    SciTech Connect (OSTI)

    Freels, James D; Jain, Prashant K; Hobbs, Randy W

    2012-01-01

    The Oak Ridge National Laboratory (ORNL)is developing technology to produce plutonium-238 for the National Aeronautics and Space Administration (NASA) as a power source material for powering vehicles while in deep-space[1]. The High Flux Isotope Reactor (HFIR) of ORNL has been utilized to perform test irradiations of incapsulated neptunium oxide (NpO2) and aluminum powder bare pellets for purposes of understanding the performance of the pellets during irradiation[2]. Post irradiation examinations (PIE) are currently underway to assess the effect of temperature, thermal expansion, swelling due to gas production, fission products, and other phenomena

  19. I. Nuclear Production Reaction and Chemical Isolation Procedure for 240Am II. New Superheavy Element Isotopes: 242Pu(48Ca,5n)285-114

    E-Print Network [OSTI]

    Ellison, Paul Andrew

    2011-01-01

    library for nuclear science and technology. Nuclear DataJournal of Nuclear Science and Technology, 7(10):487–499,Journal of Nuclear Science and Technology, G.T. Seaborg,

  20. ELEMENTI GENERALI La tesi pu essere scritta in italiano o in inglese. In ogni caso deve presentare un riassunto scritto sia

    E-Print Network [OSTI]

    Pettenella, Davide

    ELEMENTI GENERALI La tesi può essere scritta in italiano o in inglese. In ogni caso deve presentare della tesi è dattiloscritto su fogli in formato A4 (210 mm x 297 mm), utilizzando entrambe le facciate lavoro di tesi è consigliabile servirsi di una stampante laser. Quando conveniente, le figure e i grafici

  1. I. Nuclear Production Reaction and Chemical Isolation Procedure for 240Am II. New Superheavy Element Isotopes: 242Pu(48Ca,5n)285-114

    E-Print Network [OSTI]

    Ellison, Paul Andrew

    2011-01-01

    Nuclear Production Reaction and Chemical Isolation ProcedureNuclear Production Reaction and Chemical Isolation Procedurenuclear production reaction and chemical isolation procedure

  2. FOREST GENETICS 7(4):339342, 2000 339 A R B O R A PU B L I SH E R S

    E-Print Network [OSTI]

    correspondence should be addressed. phone: (906)-487-3082; fax: (906)-487-2897; e-mail: anoormet@mtu.edu Received), formed at the interaction of nitrogen oxid es, volatile hydrocarbons and ultraviolet radiation- tional integrity of the cell. W hile the increased rise in tropospheric O3 and the resulting increase

  3. R-matrix analysis of the {sup 240}Pu neutron cross sections in the thermal to 5700 eV energy range

    SciTech Connect (OSTI)

    Derrien, H.; Bouland, O.; Larson, N.M.; Leal, L.C.

    1997-08-01

    Resonance analysis of high resolution neutron transmission data and of fission cross sections were performed in the neutron energy range from the thermal regions to 5,700 eV by using the Reich-Moore Bayesian code SAMMY. The experimental data base is described and the method of analysis is given. The experimental data were carefully examined in order to identify more resonances than those found in the current evaluated data files. The statistical properties of the resonance parameters are given. A new set of the average values of the parameters is proposed, which could be used for calculation of the average cross sections in the unresolved resonance region. The resonance parameters are available IN ENDF-6 format at the national or international data centers.

  4. Preliminary Simulations for Geometric Optimization of a High-Energy Delayed Gamma Spectrometer for Direct Assay of Pu in Spent Nuclear Fuel

    SciTech Connect (OSTI)

    Kulisek, Jonathan A.; Campbell, Luke W.; Rodriguez, Douglas C.

    2012-06-07

    High-energy, beta-delayed gamma-ray spectroscopy is under investigation as part of the Next Generation Safeguard Initiative effort to develop non-destructive assay instruments for plutonium mass quantification in spent nuclear fuel assemblies. Results obtained to date indicate that individual isotope-specific signatures contained in the delayed gamma-ray spectra can potentially be used to quantify the total fissile content and individual weight fractions of fissile and fertile nuclides present in spent fuel. Adequate assay precision for inventory analysis can be obtained using a neutron generator of sufficient strength and currently available detection technology. In an attempt to optimize the geometric configuration and material composition for a delayed gamma measurement on spent fuel, the current study applies MCNPX, a Monte Carlo radiation transport code, in order to obtain the best signal-to-noise ratio. Results are presented for optimizing the neutron spectrum tailoring material, geometries to maximize thermal or fast fissions from a given neutron source, and detector location to allow an acceptable delayed gamma-ray signal while achieving a reasonable detector lifetime while operating in a high-energy neutron field. This work is supported in part by the Next Generation Safeguards Initiative, Office of Nuclear Safeguards and Security, National Nuclear Security Administration.

  5. Pattern Recognition, Vol. 30, No. 9, pp. 1505-1519, 1997 1997 Pattern Recognition Society. PuNished by Elsevier Science Ltd

    E-Print Network [OSTI]

    Chamzas, Christodoulos

    l B. GATOS, t4 N. PAPAMARKOS t'* and C. CHAMZAS ~ tElectric Circuits Analysis Laboratory, Department

  6. Environmental considerations associated with siting, constructing, and operating a special isotope separation plant at INEL: Volume 2, Proceedings: Report of public hearings. [AVLIS; Pu isotopes

    SciTech Connect (OSTI)

    Not Available

    1987-03-01

    This report documents the two public hearings conducted for the purpose of determining the scope of issues to be addressed in relation to the siting, constructing, and operating of a special isotope separation plant at INEL. The report includes transcripts of the public hearings held in Idaho Falls, Idaho, February 24, 1987, and in Boise, Idaho, February 26, 1987, and includes the exhibits of record relating to those hearings. The review and hearing process meets pertinent National Environmental Policy Act (NEPA) requirements, Council on Environmental Quality (CEQ) regulations, and DOE guidelines.

  7. Environmental considerations associated with siting, constructing, and operating a special isotope separation plant at INEL: Volume 1, Proceedings: Report of public hearings. [AVLIS; Pu isotopes

    SciTech Connect (OSTI)

    Not Available

    1987-03-01

    This report documents the two public hearings conducted for the purpose of determining the scope of issues to be addressed in relation to the siting, constructing, and operating of a special isotope separation plant at INEL. The report includes transcripts of the public hearings held in Idaho Falls, Idaho, February 24, 1987, and in Boise, Idaho, February 26, 1987, and includes the exhibits of records relating to those hearings. The review and hearing process meets pertinent National Environmental Policy Act (NEPA) requirements, Council on Environmental Quality (CEQ) regulations, and DOE guidelines.

  8. Study of Pu consumption in advanced light water reactors: Evaluation of GE advanced boiling water reactor plants - compilation of Phase 1B task reports

    SciTech Connect (OSTI)

    1993-09-15

    This report contains an extensive evaluation of GE advanced boiling water reactor plants prepared for United State Department of Energy. The general areas covered in this report are: core and system performance; fuel cycle; infrastructure and deployment; and safety and environmental approval.

  9. Worlds of Desire: Gender and Sexuality in Classical Tamil Poetry

    E-Print Network [OSTI]

    Segran, Elizabeth Rani

    2011-01-01

    r, translated by George Hart and Hank Heifetz. Pu"an! 'r, translated by George Hart and Hank Heifetz. Pu"an! '$"ur, translated by George Hart and Hank Heifetz. Pu"an! '$"u

  10. Fusion Engineering and Design 85 (2010) 14881491 Contents lists available at ScienceDirect

    E-Print Network [OSTI]

    Abdou, Mohamed

    2010-01-01

    of the fissile TRUs (239Pu, 241Pu) in LWRs. On the other hand, the non-fissile TRUs have rele- vant fission cross

  11. Deep-Sea Research I 51 (2004) 17691780 Sedimentation in the Southern Okinawa Trough: enhanced

    E-Print Network [OSTI]

    Huh, Chih-An

    2004-01-01

    and the subsurface maximum of 240 Pu/239 Pu caused by close-in fallout from neutron-rich thermonuclear tests

  12. Nuclear Resonance Fluorescence for Materials Assay

    E-Print Network [OSTI]

    Quiter, Brian

    2010-01-01

    reprocessing facilities, the measurement of Pu and U concentration in spent fuelreprocessing techniques, new assay methods are needed to measure Pu content in spent fuel

  13. Lattice relaxation and the stability of plutonium-based alloys and intermetallics

    SciTech Connect (OSTI)

    Becker, J.D.; Cox, L.; Wills, J.M. [Los Alamos National Lab., NM (United States); Cooper, B.R. [West Virginia Univ., Morgantown, WV (United States)

    1996-12-01

    The topic of this study is the electronic structure of the compounds Pu{sub 3}X [X = In, Ga, Al, or Tl], reported to have room temperature L1{sub 2} structures. The measured Pu-Pu bond length in {delta}-phase Pu is 3.28 {Angstrom}. The Pu-Pu bond lengths in Pu{sub 3}Ga and Pu{sub 3}Al are 3.18 {Angstrom}. The similarity in bonding in Pu{sub 3}Ga and Pu{sub 3}Al is especially notable as the equilibrium atomic volume in Ga is 18% higher than that of Al. Likewise, in Pu{sub 3}In and Pu{sub 3}Tl the bond lengths are 3.33 {Angstrom} and 3.32 {Angstrom}, respectively, although the atomic volumes of In and Tl differ by 10%. The electronic mechanism by which the 8 stabilizers Al and Ga contract the Pu-Pu bonds and whereby In and Tl stretch them may relate the stability of pure Pu to that of the Pu{sub 3}X compounds. For example, does the addition of Ga or Al shorten the bond length enough to make the close-packed Ll{sub 2} structure more stable than does the addition of In or Tl? The incipient localization of the f electrons and the stabilization of open structures may be indicated through LDA total energies and densities of states.

  14. Radiation-induced non-equilibrium redox chemistry of plutonium: implications for environmental migration

    SciTech Connect (OSTI)

    Haschke, J M; Siekhaus, W J

    2009-02-11

    Static concentrations of plutonium oxidation states in solution and at surfaces in oxide-water systems are identified as non-equilibrium steady states. These kinetically controlled systems are described by redox cycles based on irreversible disproportionation of Pu(IV), Pu(V), and Pu(VI) in OH-bridged intermediate complexes and at OH-covered oxide surfaces. Steady state is fixed by continuous redox cycles driven by radioactivity-promoted electron-transfer and energetically favorable reactions of Pu(III) and Pu(VII) disproportionation products with H2O. A model based on the redox cycles accounts for the high steady-state [Pu] coexisting with Pu(IV) hydrous oxide at pH 0-15 and for predominance of Pu(V) and Pu(VI) in solution. The steady-state [Pu] depends on pH and the surface area of oxide in solution, but not on the initial Pu oxidation state. PuO{sub 2+x} formation is attributed to high Pu(V) concentrations existing at water-exposed oxide surfaces. Results infer that migration of Pu in an aqueous environment is controlled by kinetic factors unique to that site and that the predominant oxidation states in solution are Pu(V) and Pu(VI).

  15. MECCANICA DEI FLUIDI 0. Notazioni

    E-Print Network [OSTI]

    Bartocci, Claudio

    le due leggi della termodinamica, come si pu`o comunque verificare esplicitamente. Il bilancio della

  16. Experimental studies of actinide volatilities with application to mixed waste oxidation processors

    SciTech Connect (OSTI)

    Krikorian, O.H.; Ebbinghaus, B.B.; Condit, R.H.; Adamson, M.G.; Fontes, A.S. Jr.; Fleming, D.L.

    1993-04-30

    The transpiration technique is used to measure volatilities of U from U{sub 3}O{sub 8}(s), Pu from PuO{sub 2}(s) and Pu and Am from PuO{sub 2}/2%AmO{sub 2}(s) in the presence of steam and oxygen at temperatures ranging from 900 to 1300{degree}C.

  17. JADWIN HALL RENOVATIONS CORRIDOR DESIGN PROPOSALS

    E-Print Network [OSTI]

    Petta, Jason

    ? ? PU-YY13 102 PU-R14 PU-T10 101 SHAFT 5 SH-5 STAIR 5 ST-5 103A PU-W34 ELEV 2 EL-2 ELEV 1 EL-1 STAIR 1 ST-1 125B 125 125D 125A SHAFT 6 SH-6125C 124 124A 123 122121120104119 PU-U45 SHAFT 7 SH-7105A105D 105C 105 105 PU-U48PU-Y48 118118B 118A 105B 106 SHAFT 8 SH-8 117116 107 108 SHAFT 9 SH-9 109 LAB 115114

  18. The Magazine of The Johns hopkins BlooMBerg school of puBlic healTh www.jhsph.eduspring 2013 the virus that owns the world looking for trouble saving a saCred river

    E-Print Network [OSTI]

    Bushman, Frederic

    2013 15 The 2-year-old girl arrived at Phebe Hospital in rural Liberia barely alive. Her abdomen had," says Abdullah, who was in Liberia leading a medical education program to train surgeons in a cost the global surgical gap is a public health issue. "If a kid in Sierra Leone, Liberia or Su- dan falls out

  19. nature CHeMICaL BIOLOGY | vol 10 | april 2014 | www.nature.com/naturechemicalbiology 273 puBLIsHed OnLIne: 23 feBruarY 2014 | dOI: 10.1038/nCHeMBIO.1458

    E-Print Network [OSTI]

    Cai, Long

    driving force for pore opening. Desensitization has been accounted for by structural rearrangements on the functional state of a receptor and their cooperative interactions are often difficult to assess because and structural studies2,8,9 . The four ligand-binding domains (LBDs) are organized as a pair of dimers. Ligands

  20. The Magazine of The Johns hopkins BlooMBerg school of puBlic healTh www.jhsph.eduspecial death and data death and lifespan death and learning

    E-Print Network [OSTI]

    Scharfstein, Daniel

    death and data · death and lifespan · death and learning the poetry of life "Because i could not stoP for deatH" #12;MAKE A PROMISE FOR THE FUTURE Fund a Charitable Gift Annuity with a minimum gift of $10 contribution to the Johns Hopkins Bloomberg School of Public Health. Charitable Gift Annuity Rates

  1. Parameters of Cascade Gamma-Decay of Compound-Nuclei Nd-146, Gd-156, Yb-172, Ta-182, W-184, Os-191, Th-231,233, U-239, Pu-240 from Experimental Data of Reaction $(n,?)$

    E-Print Network [OSTI]

    A. M. Sukhovoj; V. A. Khitrov

    2009-06-17

    Re-analysis of experimental data on primary gamma-transitions averaged over some energy intervals of neutron resonances has been performed. Approximation of their cumulative sums together with extrapolation of the obtained distribution to zero value allowed us to determine mean intensities of of E1- and M1-transitions, their probable number and total dispersion of intensity deviations from the mean value. The level density and sum of radiative strength functions determined in this way confirm main peculiarities of these nuclear parameters determined from intensities of the two-step gamma-cascades.

  2. A Method to Calculate Fission-Fragment Yields $Y(Z,N)$ versus Proton and Neutron Number in the Brownian Shape-Motion Model. Application to calculations of U and Pu charge yields

    E-Print Network [OSTI]

    Moller, P

    2015-01-01

    We propose a method to calculate the two-dimensional (2D) fission-fragment yield $Y(Z,N)$ versus both proton and neutron number, with inclusion of odd-even staggering effects in both variables. The approach is to use Brownian shape-motion on a macroscopic-microscopic potential-energy surface which, for a particular compound system is calculated versus four shape variables: elongation (quadrupole moment $Q_2$), neck $d$, left nascent fragment spheroidal deformation $\\epsilon_{\\rm f1}$, right nascent fragment deformation $\\epsilon_{\\rm f2}$ and two asymmetry variables, namely proton and neutron numbers in each of the two fragments. The extension of previous models 1) introduces a method to calculate this generalized potential-energy function and 2) allows the correlated transfer of nucleon pairs in one step, in addition to sequential transfer. In the previous version the potential energy was calculated as a function of $Z$ and $N$ of the compound system and its shape, including the asymmetry of the shape. We ou...

  3. A Method to Calculate Fission-Fragment Yields $Y(Z,N)$ versus Proton and Neutron Number in the Brownian Shape-Motion Model. Application to calculations of U and Pu charge yields

    E-Print Network [OSTI]

    P. Moller; T. Ichikawa

    2015-08-24

    We propose a method to calculate the two-dimensional (2D) fission-fragment yield $Y(Z,N)$ versus both proton and neutron number, with inclusion of odd-even staggering effects in both variables. The approach is to use Brownian shape-motion on a macroscopic-microscopic potential-energy surface which, for a particular compound system is calculated versus four shape variables: elongation (quadrupole moment $Q_2$), neck $d$, left nascent fragment spheroidal deformation $\\epsilon_{\\rm f1}$, right nascent fragment deformation $\\epsilon_{\\rm f2}$ and two asymmetry variables, namely proton and neutron numbers in each of the two fragments. The extension of previous models 1) introduces a method to calculate this generalized potential-energy function and 2) allows the correlated transfer of nucleon pairs in one step, in addition to sequential transfer. In the previous version the potential energy was calculated as a function of $Z$ and $N$ of the compound system and its shape, including the asymmetry of the shape. We outline here how to generalize the model from the "compound-system" model to a model where the emerging fragment proton and neutron numbers also enter, over and above the compound system composition.

  4. Aspects of plutonium solution chemistry

    SciTech Connect (OSTI)

    Choppin, G.R.

    1983-01-01

    The effect of pH and complexation on the relative stabilities of the oxidation states of Pu is discussed. A set of ionic radii are presented for Pu in different oxidation states and different coordination numbers. A model for Pu hydration is presented and the relation between hydrolysis and oxidation state evaluated, including the problem of hydrous polymerization. Complexation of Pu is discussed in terms of the relative stabilities of different oxidation states and the effective ionic charge of PuO/sub 2//sup +/ and PuO/sub 2//sup +2/. An equation is proposed for calculating stability constants of Pu complexes and its correlation with experimental values demonstrated. The competition between inner vs outer sphere complexation as affected by the oxidation state of Pu and the pKa of the ligand is reviewed. Two examples of uses of specific complexing agents for Pu indicate a useful direction for future studies. 29 references, 8 figures, 3 tables.

  5. Sorption Behavior and Morphology of Plutonium in the Presence of Goethite at 25 and 80C

    SciTech Connect (OSTI)

    Zavarin, M; Zhao, P; Dai, Z; Carroll, S A; Kersting, A B

    2012-06-11

    In this study, we examined the sorption behavior of Pu at elevated temperatures in the presence of one relevant mineral, goethite ({alpha}-FeOOH), over a range of concentrations that span solubility-controlled to adsorption-controlled concentrations. We focused on the sorptive behavior of two common forms of Pu: aqueous Pu(IV) and intrinsic Pu(IV) nano-colloids at 25 and 80 C in a dilute pH 8 NaCl/NaHCO{sub 3} solution. The morphology of Pu sorbed to goethite was characterized using transmission electron microscopy (TEM). We examined the relative stability of PuO{sub 2} precipitates, PuO{sub 2} nano-colloids, Pu{sub 4}O{sub 7} surface precipitates, and monomeric sorbed Pu as a function of temperature and over a time scale of months.

  6. UPWARD MOVEMENT OF PLUTONIUM TO SURFACE SEDIMENTS DURING AN 11-YEAR FIELD STUDY

    SciTech Connect (OSTI)

    Kaplan, D.; Beals, D.; Cadieux, J.; Halverson, J.

    2010-01-25

    An 11-y lysimeter study was established to monitor the movement of Pu through vadose zone sediments. Sediment Pu concentrations as a function of depth indicated that some Pu moved upward from the buried source material. Subsequent numerical modeling suggested that the upward movement was largely the result of invading grasses taking up the Pu and translocating it upward. The objective of this study was to determine if the Pu of surface sediments originated from atmosphere fallout or from the buried lysimeter source material (weapons-grade Pu), providing additional evidence that plants were involved in the upward migration of Pu. The {sup 240}Pu/{sup 239}Pu and {sup 242}Pu/{sup 239}Pu atomic fraction ratios of the lysimeter surface sediments, as determined by Thermal Ionization Mass Spectroscopy (TIMS), were 0.063 and 0.00045, respectively; consistent with the signatures of the weapons-grade Pu. Our numerical simulations indicate that because plants create a large water flux, small concentrations over multiple years may result in a measurable accumulation of Pu on the ground surface. These results may have implications on the conceptual model for calculating risk associated with long-term stewardship and monitored natural attenuation management of Pu contaminated subsurface and surface sediments.

  7. Plutonium Oxidation and Subsequent Reduction by Mn (IV) Minerals

    SciTech Connect (OSTI)

    KAPLAN, DANIEL

    2005-09-13

    Plutonium sorbed to rock tuff was preferentially associated with manganese oxides. On tuff and synthetic pyrolusite (Mn{sup IV}O{sub 2}), Pu(IV) or Pu(V) was initially oxidized, but over time Pu(IV) became the predominant oxidation state of sorbed Pu. Reduction of Pu(V/VI), even on non-oxidizing surfaces, is proposed to result from a lower Gibbs free energy of the hydrolyzed Pu(IV) surface species versus that of the Pu(V) or Pu(VI) surface species. This work suggests that despite initial oxidation of sorbed Pu by oxidizing surfaces to more soluble forms, the less mobile form of Pu, Pu(IV), will dominate Pu solid phase speciation during long term geologic storage. The safe design of a radioactive waste or spent nuclear fuel geologic repository requires a risk assessment of radionuclides that may potentially be released into the surrounding environment. Geochemical knowledge of the radionuclide and the surrounding environment is required for predicting subsurface fate and transport. Although difficult even in simple systems, this task grows increasingly complicated for constituents, like Pu, that exhibit complex environmental chemistries. The environmental behavior of Pu can be influenced by complexation, precipitation, adsorption, colloid formation, and oxidation/reduction (redox) reactions (1-3). To predict the environmental mobility of Pu, the most important of these factors is Pu oxidation state. This is because Pu(IV) is generally 2 to 3 orders of magnitude less mobile than Pu(V) in most environments (4). Further complicating matters, Pu commonly exists simultaneously in several oxidation states (5, 6). Choppin (7) reported Pu may exist as Pu(IV), Pu(V), or Pu(VI) oxic natural groundwaters. It is generally accepted that plutonium associated with suspended particulate matter is predominantly Pu(IV) (8-10), whereas Pu in the aqueous phase is predominantly Pu(V) (2, 11-13). The influence of the character of Mn-containing minerals expected to be found in subsurface repository environments on Pu oxidation state distributions has been the subject of much recent research. Kenney-Kennicutt and Morse (14), Duff et al. (15), and Morgenstern and Choppin (16) observed oxidation of Pu facilitated by Mn(IV)-bearing minerals. Conversely, Shaughnessy et al. (17) used X-ray Absorption near-edge spectroscopy (XANES) to show reduction of Pu(VI) by hausmannite (Mn{sup II}Mn{sub 2}{sup III}O{sub 4}) and manganite ({gamma}-Mn{sup III}OOH) and Kersting et al., (18) observed reduction of Pu(VI) by pyrolusite (Mn{sup IV}O{sub 2}). In this paper, we attempt to reconcile the apparently conflicting datasets by showing that Mn-bearing minerals can indeed oxidize Pu, however, if the oxidized species remains on the solid phase, the oxidation step competes with the formation of Pu(IV) that becomes the predominant solid phase Pu species with time. The experimental approach we took was to conduct longer term (approximately two years later) oxidation state analyses on the Pu sorbed to Yucca Mountain tuff (initial analysis reported by Duff et al., (15)) and measure the time-dependant changes in the oxidation state distribution of Pu in the presence of the Mn mineral pyrolusite.

  8. Glenn T. Seaborg - Patents - 1954 through 1958

    Office of Scientific and Technical Information (OSTI)

    for concentrating dilute solutions of Pu. The process consists of alternately using La salt precipitate and Nb2O5 precipitates as carriers for the Pu, and of redissolving each...

  9. EA-0534: Radioisotope Heat Source Fuel Processing and Fabrication, Los Alamos, New Mexico

    Broader source: Energy.gov [DOE]

    This EA evaluates the environmental impacts of a proposal to operate existing Pu-238 processing facilities at Savannah River Site, and fabricate a limited quantity of Pu-238 fueled heat sources at...

  10. MOX Fuel Presentation to Duke Board of Directors

    National Nuclear Security Administration (NNSA)

    PuO 2 with 95% depleted UO 2 - Like LEU fuel pellets, MOX fuel pellets are primarily uranium * Fission power comes primarily from plutonium (Pu 239 ) instead of uranium (U 235 )...

  11. Stabilities of the Aqueous Complexes Cm(CO3)3 and Am(CO3)3

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    /T reflecting negligible temperature influence on the corresponding molar enthalpy change rH3 = 12+ (28%), Pu(OH)2 + (21%) and PuCO3 + (19%). Thermochemical databases have been constructed from

  12. Entropia e irreversibilit`a Giovanni Gallavotti

    E-Print Network [OSTI]

    Roma "La Sapienza", Università di

    dell'Accademia, non pu`o mai essere ignorato. 2. Fisica e Metafisica Credo che la semplice spiegazione

  13. A version of this appeared in Current Science 75(6) 1998 India's Nuclear Breeders: Technology, Viability, and Options

    E-Print Network [OSTI]

    , for the U238-Pu cycle, only metallic fuel offers hope of rapid increase in available fissile material

  14. Algoritmi e Strutture Dati Esercizio 1

    E-Print Network [OSTI]

    Montresor, Alberto

    Questo problema si pu`o risolvere efficientemente applicando l'algoritmo di visita in ampiezza (BFS) di

  15. Algoritmi e Strutture Dati -Seconda provetta Esercizio 1

    E-Print Network [OSTI]

    Montresor, Alberto

    completezza) pu`o essere scritta nel modo seguente. Notate che ne esiste una versione pi`u efficiente che

  16. SEGNALI E WAVELET Nota di CARLA GUERRINI

    E-Print Network [OSTI]

    Guerrini, Carla

    vedere un segnale a differenti scale o riso­luzioni, in una rappresentazione grossolana il segnale pu

  17. Natural and anthropogenic radionuclides in the marginal seas of Siberia: implications for the fate and removal of pollutants 

    E-Print Network [OSTI]

    Schwantes, Jon Michael

    1996-01-01

    understand scavenging within the water column. To elucidate the sources of Pu and 131CS to the study area, Pu and "'Cs concentrations and 238PU/239,240puactivity ratios were measured in water samples. Concentrations of Ra isotopes were also determined...

  18. U238 (1) (2)

    E-Print Network [OSTI]

    Hong, Deog Ki

    Silver 4.21 x 101 2.75 x 103 4.16 x 101 Cadmium 4.75 x 101 5.95 x 101 2.13 x 10-1 Indium 1.09 3.57 x 10 . - , , , . . . Ferrous sulfamate, Hydroxylamine nitrate Pu(IV) Pu(III) Pu

  19. ISOTOPESuses, demand, and supply NIST Center for Neutron Research

    E-Print Network [OSTI]

    Dimeo, Robert M.

    incremental loss of storage capacity significant loss of storage capacity 1 2, 3, ... #12;Li-ion battery Pa-233 Pm-147 Pu-236 Pu-242 Pu-244 Re-186 Sn-117m Th-230 Th-232 U-232 W-188 #12;Li-ion battery

  20. Cooperative Spectrum Sharing: A Contract-based Approach

    E-Print Network [OSTI]

    Huang, Jianwei

    study the optimal contract design for both weakly and strongly incomplete information scenarios information and not known by a PU. We model the PU-SU interaction as a labor market using contract theory. In the weakly incomplete information scenario, we show that the PU will optimally hire the most efficient SUs

  1. Management Overview

    Office of Environmental Management (EM)

    0 2 4 6 8 10 12 0 2 4 6 8 10 12 Pu(IV), mM Pu(IV), mM predicted Pu(IV), mM, model Static measurements: Model training database Chemometric model development On-line model...

  2. Possible differences in biological availability of isotopes of plutonium: Report of a workshop

    SciTech Connect (OSTI)

    Kercher, J.R.; Gallegos, G.M.

    1993-09-01

    This paper presents the results of a workshop conducted on the apparent different bioavailability of isotopes {sup 238}Pu and {sup 239}Pu. There is a substantial body of evidence that {sup 238}Pu as commonly found in the environment is more biologically available than {sup 239}Pu. Studies of the Trinity Site, Nevada Test Site from nonnuclear and nuclear events, Rocky Flats, Enewetak and Bikini, and the arctic tundra support this conclusion and indicate that the bioavailability of {sup 238}Pu is more than an order of magnitude greater than that of {sup 239}Pu. Plant and soil studies from controlled environments and from Savannah River indicate no isotopic difference in availability of Pu to plants; whereas studies at the Trinity Site do suggest a difference. While it is possible that these observations can be explained by problems in the experimental procedure and analytical techniques, this possibility is remote given the ubiquitous nature of the observations. Studies of solubility of Pu in the stomach contents of cattle grazing at the Nevada Test Site and from fish from Bikini Atoll both found that {sup 238}Pu was more soluble than {sup 239}Pu. Studies of the Los Alamos effluent stream indicate that as particle size decreases, the content of {sup 238}Pu relative to {sup 239}Pu increases.

  3. QUEEN'S UNIVERSITY DOCTORAL COTUTELLE AGREEMENT

    E-Print Network [OSTI]

    Fletcher, Robin

    .... to ...... PU from ..... to ..... Queen's from .... to ...... 1.3 Tuition and Ancillary Fees Tuition and ancillary fees are paid to Queen's University for the duration of the program. If a Queen's student while at PU is charged tuition and ancillary fees at the PU, the student may apply for a tuition waiver from

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

    SciTech Connect (OSTI)

    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.

  5. SU-E-I-49: The Evaluation of Usability of Multileaf Collimator for Diagnostic Radiation in Cephalometric Exposure

    SciTech Connect (OSTI)

    Han, S; Kim, K; Jung, H; Kim, M; Ji, Y; Park, S; Choi, S

    2014-06-01

    Purpose: This study evaluated usability of Multileaf collimator (MLC) for diagnostic radiation in cephalometric exposure using optical stimulated luminance dosimeters (OSLDs) Methods: The MLC material was made alloy tool steel (SKD-11) and the density of it is 7.89g/m3 that is similar to it of steel (Fe, 7.85 g/m3) and the MLC was attached to general radiography unit (Rex-650R, Listem Inc, Korea) for cephalometric exposure. The OSLDs that used were nanoDotTM Dosimeter (Landauer Inc, Glenwood, USA) and we read out OSLDs with micro star system (Landauer Inc, Glenwood, USA). The Optical annealing system contained fluorescent lamps (Osram lumilux, 24 W, 280 ?780 nm). To measure absorbed dose using OSLDs, was carried out dosimetric characteristics of OSLDs. Based on these, we evaluated dose reduction of critical organ (Eyes, Thyroids) with MLC in cephalometric exposure Results: The dosimetric characteristics were following that batch homogeneity was 1.21% and reproducibility was 0.96% of the coefficient of variation The linearity was that the correlation of between dose and count was fitted by linear function (dose,mGy = 0.00029 × Count, R2 =0.997). The range of angular dependence was from ?3.6% to 3.7% variation when each degree was normalized by zero degree. The organ dose of Rt. eye, Lt eye, thyroids were 77.8 ?Gy, 337.0 ?Gy, 323.1?Gy, respectively in open field and the dose reduction of organ dose was 10.6%(8.3?Gy), 12.4 %(42 ?Gy), 87.1%(281.4?Gy) with MLC Conclusion: We certified dose reduction of organ dose in cephalometric exposure. The dose reduction of Eye was 11% because of reduction of field size and it of thyroids was 87% by primary beam shielding.

  6. Plutonium Metallurgy

    SciTech Connect (OSTI)

    Freibert, Franz J. [Los Alamos National Laboratory

    2012-08-09

    Due to its nuclear properties, Pu will remain a material of global interest well into the future. Processing, Structure, Properties and Performance remains a good framework for discussion of Pu materials science Self-irradiation and aging effects continue to be central in discussions of Pu metallurgy Pu in its elemental form is extremely unstable, but alloying helps to stabilize Pu; but, questions remain as to how and why this stabilization occurs. Which is true Pu-Ga binary phase diagram: US or Russian? Metallurgical issues such as solute coring, phase instability, crystallographic texture, etc. result in challenges to casting, processing, and properties modeling and experiments. For Ga alloyed FCC stabilized Pu, temperature and pressure remain as variables impacting phase stability.

  7. A Neutronic Analysis of TRU Recycling in PWRs Loaded with MOX-UE Fuel (MOX with U-235 Enriched U Support)

    SciTech Connect (OSTI)

    G. Youinou; S. Bays

    2009-05-01

    This report presents the results of a study dealing with the homogeneous recycling of either Pu or Pu+Np or Pu+Np+Am or Pu+Np+Am+Cm in PWRs using MOX-UE fuel, i.e. standard MOX fuel with a U235 enriched uranium support instead of the standard tail uranium (0.25%) for standard MOX fuel. This approach allows to multirecycle Pu or TRU (Pu+MA) as long as U235 is available, by keeping the Pu or TRU content in the fuel constant and at a value ensuring a negative moderator void coefficient (i.e. the loss of the coolant brings imperatively the reactor to a subcritical state). Once this value is determined, the U235 enrichment of the MOX-UE fuel is adjusted in order to reach the target burnup (51 GWd/t in this study).

  8. PLUTONIUM SOLUBILITY IN HIGH-LEVEL WASTE ALKALI BOROSILICATE GLASS

    SciTech Connect (OSTI)

    Marra, J.; Crawford, C.; Fox, K.; Bibler, N.

    2011-01-04

    The solubility of plutonium in a Sludge Batch 6 (SB6) reference glass and the effect of incorporation of Pu in the glass on specific glass properties were evaluated. A Pu loading of 1 wt % in glass was studied. Prior to actual plutonium glass testing, surrogate testing (using Hf as a surrogate for Pu) was conducted to evaluate the homogeneity of significant quantities of Hf (Pu) in the glass, determine the most appropriate methods to evaluate homogeneity for Pu glass testing, and to evaluate the impact of Hf loading in the glass on select glass properties. Surrogate testing was conducted using Hf to represent between 0 and 1 wt % Pu in glass on an equivalent molar basis. A Pu loading of 1 wt % in glass translated to {approx}18 kg Pu per Defense Waste Processing Facility (DWPF) canister, or about 10X the current allowed limit per the Waste Acceptance Product Specifications (2500 g/m{sup 3} of glass or about 1700 g/canister) and about 30X the current allowable concentration based on the fissile material concentration limit referenced in the Yucca Mountain Project License Application (897 g/m{sup 3}3 of glass or about 600 g Pu/canister). Based on historical process throughput data, this level was considered to represent a reasonable upper bound for Pu loading based on the ability to provide Pu containing feed to the DWPF. The task elements included evaluating the distribution of Pu in the glass (e.g. homogeneity), evaluating crystallization within the glass, evaluating select glass properties (with surrogates), and evaluating durability using the Product Consistency Test -- Method A (PCT-A). The behavior of Pu in the melter was evaluated using paper studies and corresponding analyses of DWPF melter pour samples.The results of the testing indicated that at 1 wt % Pu in the glass, the Pu was homogeneously distributed and did not result in any formation of plutonium-containing crystalline phases as long as the glass was prepared under 'well-mixed' conditions. The incorporation of 1 wt % Pu in the glass did not adversely impact glass viscosity (as assessed using Hf surrogate) or glass durability. Finally, evaluation of DWPF glass pour samples that had Pu concentrations below the 897 g/m{sup 3} limit showed that Pu concentrations in the glass pour stream were close to targeted compositions in the melter feed indicating that Pu neither volatilized from the melt nor stratified in the melter when processed in the DWPF melter.

  9. Development of a Composite Non-Electrostatic Surface Complexation Model Describing Plutonium Sorption to Aluminosilicates

    SciTech Connect (OSTI)

    Powell, B A; Kersting, A; Zavarin, M; Zhao, P

    2008-10-28

    Due to their ubiquity in nature and chemical reactivity, aluminosilicate minerals play an important role in retarding actinide subsurface migration. However, very few studies have examined Pu interaction with clay minerals in sufficient detail to produce a credible mechanistic model of its behavior. In this work, Pu(IV) and Pu(V) interactions with silica, gibbsite (Aloxide), and Na-montmorillonite (smectite clay) were examined as a function of time and pH. Sorption of Pu(IV) and Pu(V) to gibbsite and silica increased with pH (4 to 10). The Pu(V) sorption edge shifted to lower pH values over time and approached that of Pu(IV). This behavior is apparently due to surface mediated reduction of Pu(V) to Pu(IV). Surface complexation constants describing Pu(IV)/Pu(V) sorption to aluminol and silanol groups were developed from the silica and gibbsite sorption experiments and applied to the montmorillonite dataset. The model provided an acceptable fit to the montmorillonite sorption data for Pu(V). In order to accurately predict Pu(IV) sorption to montmorillonite, the model required inclusion of ion exchange. The objective of this work is to measure the sorption of Pu(IV) and Pu(V) to silica, gibbsite, and smectite (montmorillonite). Aluminosilicate minerals are ubiquitous at the Nevada National Security Site and improving our understanding of Pu sorption to aluminosilicates (smectite clays in particular) is essential to the accurate prediction of Pu transport rates. These data will improve the mechanistic approach for modeling the hydrologic source term (HST) and provide sorption Kd parameters for use in CAU models. In both alluvium and tuff, aluminosilicates have been found to play a dominant role in the radionuclide retardation because their abundance is typically more than an order of magnitude greater than other potential sorbing minerals such as iron and manganese oxides (e.g. Vaniman et al., 1996). The sorption database used in recent HST models (Carle et al., 2006) and upscaled for use in CAU models (Stoller-Navarro, 2008) includes surface complexation constants for U, Am, Eu, Np and Pu (Zavarin and Bruton, 2004). Generally, between 15 to 30 datasets were used to develop the constants for each radionuclide. However, the constants that describe Pu sorption to aluminosilicates were developed using only 10 datasets, most of which did not specify the oxidation state of Pu in the experiment. Without knowledge or control of the Pu oxidation state, a high degree of uncertainty is introduced into the model. The existing Pu surface complexation model (e.g. Zavarin and Bruton, 2004) drastically underestimates Pu sorption and, thus, will overestimate Pu migration rates (Turner, 1995). Recent HST simulations at Cambric (Carle et al., 2006) suggest that the existing surface complexation model may underpredict Pu K{sub d}s by as much as 3 orders of magnitude. In order to improve HST and CAU-scale transport models (and, as a result, reduce the conservative nature Pu migration estimates), sorption experiments were performed over a range of solution conditions that brackets the groundwater chemistry of the Nevada National Security Site. The aluminosilicates examined were gibbsite, silica, and montmorillonite.

  10. Plutonium Transport Through Lysimeters Exposed to Natural Weather Conditions for Two to Twelve Years

    SciTech Connect (OSTI)

    Kaplan, D.I.

    2003-10-20

    One of the most important factors influencing the subsurface transport of plutonium (Pu) is its oxidation state. Under similar geochemical conditions (e.g., groundwater pH) the mobility of reduced Pu, Pu(IV), is two to three orders of magnitude lower than that of oxidized Pu, Pu(V) and Pu(VI). However, due to a poor understanding of Pu oxidation state transformations, transport models typically employ conservative assumptions which can lead to overly conservative and costly decisions. The objective of this study was to develop a conceptual geochemical transport model to describe Pu mobility through 52-L lysimeters established in 1980. The lysimeters contained E-Area sediment and various forms of well-characterized Pu sources of known oxidation state and were exposed to natural SRS weather conditions for up to 11 years. For this study, archived core sediments from the lysimeters were retrieved and Pu concentrations in depth-discrete samples were measured and then transport of Pu was modeled using a coupled reactive transport model. The geochemical conceptual model and input values included in the transport code were based on laboratory experiments. The single most important finding from this work was regardless of the Pu oxidation state added to SRS sediments, it quickly converted to the less mobile Pu(IV) form. In conclusion, it is expected that Pu will exist primarily in the SRS subsurface environment in the relatively less mobile Pu(IV) form, irrespective of the oxidation state that it first enters the ground. The lysimeter results provide important long-term data that support the removal of important overly conservative approaches presently used to calculate risk and performance assessment associated with groundwater Pu. These findings do not contradict previous Pu modeling efforts, including the E-Area Low-Level Waste Performance Assessment or the Special Analysis on Pu disposal in SRS trenches. Instead, the results from this work could be used in future calculations to improve accuracy and reduce uncertainty and conservatism.

  11. Colloidal Cutin-like Siderophoric Molecules Mobilize Plutonium from Contaminated Soils of the Rocky Flats Environmental Technology Site (RFETS), USA

    SciTech Connect (OSTI)

    Xu, C.; Santschi, P; Roberts, K; Zhong, J; Hatcher, P; Hung, C; Francis, A; Dodge, C; Honeyman, B

    2008-01-01

    Relatively recently, inorganic colloids have been invoked to reconcile the apparent contradictions between expectations based on classical dissolved-phase Pu transport and field observations of 'enhanced' Pu mobility (Kersting et al. Nature 1999, 397, 56-59). A new paradigm for Pu transport is mobilization and transport via biologically produced ligands. This study for the first time reports a new finding of Pu being transported, at sub-pM concentrations, by a cutin-like natural substance containing siderophore-like moieties and virtually all mobile Pu. Most likely, Pu is complexed by chelating groups derived from siderophores that are covalently bound to a backbone of cutin-derived soil degradation products, thus revealing the history of initial exposure to Pu. Features such as amphiphilicity and small size make this macromolecule an ideal collector for actinides and other metals and a vector for their dispersal. Cross-linking to the hydrophobic domains (e.g., by polysaccharides) gives this macromolecule high mobility and a means of enhancing Pu transport. This finding provides a new mechanism for Pu transport through environmental systems that would not have been predicted by Pu transport models.

  12. The growth and evolution of thin oxide films on delta-plutonium surfaces

    SciTech Connect (OSTI)

    Garcia Flores, Harry G [Los Alamos National Laboratory; Pugmire, David L [Los Alamos National Laboratory

    2009-01-01

    The common oxides of plutonium are the dioxide (PuO{sub 2}) and the sesquioxide (Pu{sub 2}O{sub 3}). The structure of an oxide on plutonium metal under air at room temperature is typically described as a thick PuO{sub 2} film at the gas-oxide interface with a thinner PuO{sub 2} film near the oxide-metal substrate interface. In a reducing environment, such as ultra high vacuum, the dioxide (Pu{sup 4+}; O/Pu = 2.0) readily converts to the sesquioxide (Pu{sup 3+}; O/Pu = 1.5) with time. In this work, the growth and evolution of thin plutonium oxide films is studied with x-ray photoelectron spectroscopy (XPS) under varying conditions. The results indicate that, like the dioxide, the sesquioxide is not stable on a very clean metal substrate under reducing conditions, resulting in substoichiometric films (Pu{sub 2}O{sub 3-y}). The Pu{sub 2}O{sub 3-y} films prepared exhibit a variety of stoichiometries (y = 0.2-1) as a function of preparation conditions, highlighting the fact that caution must be exercised when studying plutonium oxide surfaces under these conditions and interpreting resulting data.

  13. Wind resuspension of trace amounts of plutonium particles from soil in a semi-arid climate

    SciTech Connect (OSTI)

    Langer, G.

    1984-01-01

    This study of resuspension of soil containing minute amounts of plutonium (Pu-239) has been in progress at the Rocky Flats (RF) Plant since 1978. It is one of several studies initiated after wind relocated small amounts of soil-borne Pu-239 during cleanup of an outdoor storage area. The Pu-239-settled field is now sparsely covered with prairie grass typical of the area. Past studies were limited to comparisons of bulk soil activity with total activity in the airborne dust. This work covers the physics of the particle resuspension process. This report covers the following: (1) Pu-239 resuspension rate versus wind speed, (2) mechanisms of soil particle resuspension, (3) vertical concentration profile of Pu-239 particles, (4) Pu-239 and host particle size distribution and activity concentration. 5 references, 1 table.

  14. Plutonium management for the future

    SciTech Connect (OSTI)

    Pillay, K.K.S.

    1996-05-01

    Managment of excess nuclear materials from US weapons dismantlement has been the subject of numerous intellectual discussions during the past 5 years. Although there has been some objective recommendations, there is still much controversy surrounding the procsses that could lead to a national decision on Pu management. Two immediate needs are to secure the inventories of all Pu in safe configurations and to develop strategies for reducing proliferation risks. Specific suggestions discussed here are to (a) accept the deterrence value of Pu, (b) reappraise its potential as an energy resource, (c) recognize limitations to influence the future of Pu use world-wide, (d) isolate recoverable weapons-grade Pu and store it in stable configurations under international safeguards, and (e) manage Pu in spent fuels so that the valuable resources are not lost to a future generation.

  15. Standard test method for the determination of impurities in plutonium metal: acid digestion and inductively coupled plasma-mass spectroscopy (ICP-MS) analysis

    E-Print Network [OSTI]

    American Society for Testing and Materials. Philadelphia

    2006-01-01

    1.1 This Test Method covers the determination of 58 trace elements in plutonium (Pu) metal. The Pu sample is dissolved in acid, and the concentration of the trace impurities are determined by Inductively Coupled Plasma-Mass Spectroscopy (ICP-MS). 1.2 This Test Method is specific for the determination of trace impurities in Pu metal. It may be applied to other types of Pu materials, such as Pu oxides, if the samples are dissolved and oxidized to the Pu(IV) state. However, it is the responsibility of the user to evaluate the performance of other matrices. 1.3 This standard does not purport to address all of the safety concerns associated with its use. It is the responsibility of the user of this method to establish appropriate safety and health practices and to determine the applicability of regulatory limitations prior to use of this standard.

  16. Method for photochemical reduction of uranyl nitrate by tri-N-butyl phosphate and application of this method to nuclear fuel reprocessing

    DOE Patents [OSTI]

    De Poorter, Gerald L. (Los Alamos, NM); Rofer-De Poorter, Cheryl K. (Los Alamos, NM)

    1978-01-01

    Uranyl ion in solution in tri-n-butyl phosphate is readily photochemically reduced to U(IV). The product U(IV) may effectively be used in the Purex process for treating spent nuclear fuels to reduce Pu(IV) to Pu(III). The Pu(III) is readily separated from uranium in solution in the tri-n-butyl phosphate by an aqueous strip.

  17. Method of immobilizing weapons plutonium to provide a durable, disposable waste product

    DOE Patents [OSTI]

    Ewing, Rodney C. (Albuquerque, NM); Lutze, Werner (Albuquerque, NM); Weber, William J. (Richland, WA)

    1996-01-01

    A method of atomic scale fixation and immobilization of plutonium to provide a durable waste product. Plutonium is provided in the form of either PuO.sub.2 or Pu(NO.sub.3).sub.4 and is mixed with and SiO.sub.2. The resulting mixture is cold pressed and then heated under pressure to form (Zr,Pu)SiO.sub.4 as the waste product.

  18. Fuel element design for the enhanced destruction of plutonium in a nuclear reactor

    DOE Patents [OSTI]

    Crawford, Douglas C. (Idaho Falls, ID); Porter, Douglas L. (Idaho Falls, ID); Hayes, Steven L. (Idaho Falls, ID); Hill, Robert N. (Bolingbrook, IL)

    1999-01-01

    A uranium-free fuel for a fast nuclear reactor comprising an alloy of Pu, Zr and Hf, wherein Hf is present in an amount less than about 10% by weight of the alloy. The fuel may be in the form of a Pu alloy surrounded by a Zr--Hf alloy or an alloy of Pu--Zr--Hf or a combination of both.

  19. Fluorescence Imaging for Nuclear Arms Control Verification 

    E-Print Network [OSTI]

    Feener, Jessica S

    2014-08-14

    grade Pu typically contains more than 90% 239Pu.10 Additionally, the fissile material must be in metallic form. There are many different nuclear warhead designs, but there are three general warhead types: gun-type, implosion and thermonuclear. In a... gun-type device, two subcritical components of HEU are combined using High Explosives (HE) to make a supercritical configuration. An implosion device uses HE (also known as the physics package) to implode a spherical ‘pit’ of HEU or weapons grade Pu...

  20. X-ray absorption fine structure spectroscopic determination of plutonium speciation at the Rocky Flats environmental technology

    SciTech Connect (OSTI)

    Lezama-pacheco, Juan S; Conradson, Steven D; Clark, David L

    2008-01-01

    X-ray Absorption Fine Structure spectroscopy was used to probe the speciation of the ppm level Pu in thirteen soil and concrete samples from the Rocky Flats Environmental Technology Site in support of the site remediation effort that has been successfully completed since these measurements. In addition to X-ray Absorption Near Edge Spectra, two of the samples yielded Extended X-ray Absorption Fine Structure spectra that could be analyzed by curve-fits. Most of these spectra exhibited features consistent with PU(IV), and more specificaJly, PuO{sub 2+x}-type speciation. Two were ambiguous, possibly indicating that Pu that was originally present in a different form was transforming into PuO{sub 2+x}, and one was interpreted as demonstrating the presence of an unusual Pu(VI) compound, consistent with its source being spills from a PUREX purification line onto a concrete floor and the resultant extreme conditions. These experimental results therefore validated models that predicted that insoluble PuO{sub 2+x} would be the most stable form of Pu in equilibrium with air and water even when the source terms were most likely Pu metal with organic compounds or a Pu fire. A corollary of these models' predictions and other in situ observations is therefore that the minimal transport of Pu that occurred on the site was via the resuspension and mobilization of colloidal particles. Under these conditions, the small amounts of diffusely distributed Pu that were left on the site after its remediation pose only a negligible hazard.

  1. Fuel element design for the enhanced destruction of plutonium in a nuclear reactor

    DOE Patents [OSTI]

    Crawford, D.C.; Porter, D.L.; Hayes, S.L.; Hill, R.N.

    1999-03-23

    A uranium-free fuel for a fast nuclear reactor comprising an alloy of Pu, Zr and Hf, wherein Hf is present in an amount less than about 10% by weight of the alloy. The fuel may be in the form of a Pu alloy surrounded by a Zr--Hf alloy or an alloy of Pu--Zr--Hf or a combination of both. 7 figs.

  2. Policy Paper 09: Northeast Asia Cooperation Dialogue II Conference Papers

    E-Print Network [OSTI]

    Young-Koo, Cha; Kang, Choi; JI, Guoxing; Mack, Andrew; Pregenzer, Arian L.; Dobrovolski, Vassili

    1994-01-01

    legally stockpile separated plutonium (Pu) and highlyhidden stockpiles of already- produced plutonium. Moreover,stockpile in large quantities, but rather will import little more plutonium

  3. PowerPoint Presentation

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Technology John Begovich Safeguards and Security Technology Chris Pickett Nuclear Analytical Chemistry Joe Giaquinto Forensic Science Thrust Area: Brian Anderson Pu-238...

  4. Design of the Laboratory-Scale Plutonium Oxide Processing Unit in the Radiochemical Processing Laboratory

    SciTech Connect (OSTI)

    Lumetta, Gregg J.; Meier, David E.; Tingey, Joel M.; Casella, Amanda J.; Delegard, Calvin H.; Edwards, Matthew K.; Orton, Robert D.; Rapko, Brian M.; Smart, John E.

    2015-05-01

    This report describes a design for a laboratory-scale capability to produce plutonium oxide (PuO2) for use in identifying and validating nuclear forensics signatures associated with plutonium production, as well as for use as exercise and reference materials. This capability will be located in the Radiochemical Processing Laboratory at the Pacific Northwest National Laboratory. The key unit operations are described, including PuO2 dissolution, purification of the Pu by ion exchange, precipitation, and re-conversion to PuO2 by calcination.

  5. Search for: All records | SciTech Connect

    Office of Scientific and Technical Information (OSTI)

    ; Jack Law ; Bruce Mincher ; Steve Frank ; John Swanson The United States Department of Energy proposes to re-establish a domestic capability for producing plutonium-238 (238Pu)...

  6. Analysis of a Nuclear Accident: Fission and Activation Product Releases from the Fukushima Daiichi Nuclear Facility as Remote Indicators of Source Identification, Extent of Release, and State of Damaged Spent Nuclear Fuel

    SciTech Connect (OSTI)

    Schwantes, Jon M.; Orton, Christopher R.; Clark, Richard A.

    2011-12-05

    Evidence of the release Pu from the Fukushima Daiichi nuclear power station to the local environment and surrounding communities and estimates on fraction of total fuel inventory released

  7. Compact D-D/D-T neutron generators and their applications

    E-Print Network [OSTI]

    Lou, Tak Pui

    2003-01-01

    HEU research reactors to low enriched uranium by using highPu without U. If low-enriched uranium is used, the gain from

  8. Microsoft PowerPoint - 5_IRENE_WU_NMMSS_2014_NSTS Update.ppt...

    National Nuclear Security Administration (NNSA)

    Transaction Report. Nationally Tracked Sources Nationally Tracked Sources Examples Neutron sources for reactor startup (e.g., Pu-238Be) Calibration sources (e.g., Cs-137)...

  9. 4th Annual DOE-ERSP PI Meeting: Abstracts

    E-Print Network [OSTI]

    Hazen, Terry C.

    2009-01-01

    for Enhanced Transport of Plutonium in the Vadose Zone FredTc), uranium (U), and plutonium (Pu). Microenvironments areof Bioreduced Uranium and Plutonium Session: SLAC SFA (

  10. Self-regulating neutron coincidence counter

    DOE Patents [OSTI]

    Baron, N.

    1980-06-16

    A device for accurately measuring the mass of /sup 240/Pu and /sup 239/Pu in a sample having arbitrary moderation and mixed with various contaminants. The device utilizes a thermal neutron well counter which has two concentric rings of neutron detectors separated by a moderating material surrounding the well. Neutron spectroscopic information derived by the two rings of detectors is used to measure the quantity of /sup 239/Pu and /sup 240/Pu in device which corrects for background radiation, deadtime losses of the detector and electronics and various other constants of the system.

  11. Anticipated dose to workers for Plutonium Stabilization and Handling at PFP Project W-460

    SciTech Connect (OSTI)

    LILLY, J.T.

    1999-11-30

    Report provides estimates of expected whole body and extremity radiological dose to workers conducting planned Pu stabilization and packaging operations at PFP.

  12. Structural Characterization of and Plutonium Sorption on Mesoporous and Nanoparticulate Ferrihydrite

    E-Print Network [OSTI]

    Brogan, Luna Kestrel Schwaiger

    2012-01-01

    known that nanoparticle photocatalysis will increase withThe discovery of the photocatalysis for Pu reduction wasnoteworthy that the photocatalysis can be greatly affected

  13. Neutron Detectors for Detection of Nuclear Materials at LANL...

    Office of Science (SC) Website

    to detect small amounts of U and Pu at truck monitoring ports. This would provide a new capability in homeland defense against illicit transport of nuclear materials. Recent...

  14. "Title","Creator/Author","Publication Date","OSTI Identifier...

    Office of Scientific and Technical Information (OSTI)

    Princeton, NJ (United States)","USDOE Office of Science (SC)","70 PLASMA PHYSICS AND FUSION TECHNOLOGY Computer Simulation, Diagnostics, Edge Plasma",,"Gas-Pu -Imaging (GPI) is a...

  15. Plutonium(IV) precipitates formed in alkaline media in the presence of various anions

    SciTech Connect (OSTI)

    Krot, N.N.; Shilov, V.P.; Yusov, A.B.; Tananaev, I.G.; Grigoriev, M.S.; Garnov, A.Yu.; Perminov, V.P.; Astafurova, L.N.

    1998-09-01

    The tendency of Pu(IV) to hydrolyze and form true solutions, colloid solutions, or insoluble precipitates has been known since the Manhattan Project. Since then, specific studies have been performed to examine in detail the equilibria of Pu(IV) hydrolytic reactions in various media. Great attention also has been paid to the preparation, structure, and properties of Pu(IV) polymers or colloids. These compounds found an important application in sol-gel technology for the preparation of nuclear fuel materials. A most important result of these works was the conclusion that Pu(IV) hydroxide, after some aging, consists of very small PuO{sub 2} crystallites and should therefore be considered to be Pu(IV) hydrous oxide. However, studies of the properties and behavior of solid Pu(IV) hydroxide in complex heterogeneous systems are rare. The primary goal of this investigation was to obtain data on the composition and properties of Pu(IV) hydrous oxide or other compounds formed in alkaline media under different conditions. Such information is important to understand Pu(IV) behavior and the forms of its existence in the Hanford Site alkaline tank waste sludge. This knowledge then may be applied in assessing plutonium criticality hazards in the storage, retrieval, and treatment of Hanford Site tank wastes as well as in understanding its contribution to the transuranic waste inventory (threshold at 100 nCi/g or about 5 {times} 10{sup {minus}6} M) of the separate solution and solid phases.

  16. September 2015 Most Viewed Documents for Fission And Nuclear...

    Office of Scientific and Technical Information (OSTI)

    Fission And Nuclear Technologies Estimation of gas leak rates through very small orifices and channels. From sealed PuOsub 2 containers under accident conditions Bomelburg,...

  17. PLUTONIUM-238 RECOVERY FROM IRRADIATED NEPTUNIUM TARGETS USING...

    Office of Scientific and Technical Information (OSTI)

    proposes to re-establish a domestic capability for producing plutonium-238 (238Pu) to fuel radioisotope power systems primarily in support of future space missions. A...

  18. PLUTONIUM LOADING CAPACITY OF REILLEX HPQ ANION EXCHANGE COLUMN - AFS-2 PLUTONIUM FLOWSHEET FOR MOX

    SciTech Connect (OSTI)

    Kyser, E.; King, W.; O'Rourke, P.

    2012-07-26

    Radioactive plutonium (Pu) anion exchange column experiments using scaled HB-Line designs were performed to investigate the dependence of column loading performance on the feed composition in the H-Canyon dissolution process for plutonium oxide (PuO{sub 2}) product shipped to the Mixed Oxide (MOX) Fuel Fabrication Facility (MFFF). These loading experiments show that a representative feed solution containing {approx}5 g Pu/L can be loaded onto Reillex{trademark} HPQ resin from solutions containing 8 M total nitrate and 0.1 M KF provided that the F is complexed with Al to an [Al]/[F] molar ratio range of 1.5-2.0. Lower concentrations of total nitrate and [Al]/[F] molar ratios may still have acceptable performance but were not tested in this study. Loading and washing Pu losses should be relatively low (<1%) for resin loading of up to 60 g Pu/L. Loading above 60 g Pu/L resin is possible, but Pu wash losses will increase such that 10-20% of the additional Pu fed may not be retained by the resin as the resin loading approaches 80 g Pu/L resin.

  19. Start-up Plan for Plautonium-238 Production for Radioisotope...

    Broader source: Energy.gov (indexed) [DOE]

    The Administration has requested the restart of plutonium-238 (Pu-238) production in fiscal year (FY) 2011. The following joint start-up plan, consistent with the President's...

  20. The Life and Religious Culture of the Freshwater Boat People of North China, 1700-Present

    E-Print Network [OSTI]

    Lin, Ching-chih

    2012-01-01

    Shen shi zu pu (????[Genealogy of the Shen lineage]).is a good example. Their genealogy says the apical ancestorlower lying land. Their genealogy claims that there were

  1. Method for separating actinides. [Patent application; stripping of Np from organic extractant

    DOE Patents [OSTI]

    Friedman, H.A.; Toth, L.M.

    1980-11-10

    An organic solution used for processing spent nuclear reactor fuels is contacted with an aqueous nitric acid solution to strip Np(VI), U(VI), and Pu(IV) from the organic solution into the acid solution. The acid solution is exposed to ultraviolet light, which reduces Np(VI) to Np(V) without reducing U(VI) and Pu(IV). Since the solubility of Np(V) in the organic solution is much lower than that of Np(VI), U(VI), and Pu(IV), a major part of the Np is stripped from the organic solution while leaving most of the U and Pu therein.

  2. Determining Plutonium Mass in Spent Fuel with Nondestructive Assay Techniques NGSI Research Overview and Update on NDA Techniques

    E-Print Network [OSTI]

    A., V. Mozin, S.J. Tobin, L.W. Cambell, J.R. Cheatham, C.R. Freeman, C.J. Gesh,

    2012-01-01

    spent fuel safeguards applications, contribute to the establishment of Pu inventories and determine fissile material diversions at fuel storage, handling and reprocessing

  3. Search for: All records | SciTech Connect

    Office of Scientific and Technical Information (OSTI)

    Albert March 2015 Elasticity of Pu -a window into fundamental understanding and aging Migliori, Albert ; Saleh, Tarik A. ; Freibert, Franz J. No abstract prepared. Full...

  4. CAPABILITY TO RECOVER PLUTONIUM-238 IN H-CANYON/HB-LINE

    SciTech Connect (OSTI)

    Fuller, K.; Smith, Robert H. Jr.; Goergen, Charles R.

    2013-01-09

    Plutonium-238 is used in Radioisotope Thermoelectric Generators (RTGs) to generate electrical power and in Radioisotope Heater Units (RHUs) to produce heat for electronics and environmental control for deep space missions. The domestic supply of Pu-238 consists of scrap material from previous mission production or material purchased from Russia. Currently, the United States has no significant production scale operational capability to produce and separate new Pu-238 from irradiated neptunium-237 targets. The Department of Energy - Nuclear Energy is currently evaluating and developing plans to reconstitute the United States capability to produce Pu-238 from irradiated Np-237 targets. The Savannah River Site had previously produced and/or processed all the Pu-238 utilized in Radioisotope Thermoelectric Generators (RTGs) for deep space missions up to and including the majority of the plutonium for the Cassini Mission. The previous full production cycle capabilities included: Np-237 target fabrication, target irradiation, target dissolution and Np-237 and Pu-238 separation and purification, conversion of Np-237 and Pu-238 to oxide, scrap recovery, and Pu-238 encapsulation. The capability and equipment still exist and could be revitalized or put back into service to recover and purify Pu-238/Np-237 or broken General Purpose Heat Source (GPHS) pellets utilizing existing process equipment in HB-Line Scrap Recovery, and H-anyon Frame Waste Recovery processes. The conversion of Np-237 and Pu-238 to oxide can be performed in the existing HB-Line Phase-2 and Phase-3 Processes. Dissolution of irradiated Np-237 target material, and separation and purification of Np-237 and Pu-238 product streams would be possible at production rates of ~ 2 kg/month of Pu-238 if the existing H-Canyon Frames Process spare equipment were re-installed. Previously, the primary H-Canyon Frames equipment was removed to be replaced: however, the replacement project was stopped. The spare equipment is stored and still available for installation. Out of specification Pu-238 scrap material can be purified and recovered by utilizing the HB-Line Phase-1 Scrap Recovery Line and the Phase-3 Pu-238 Oxide Conversion Line along with H-Canyon Frame Waste Recovery process. In addition, it also covers and describes utilizing the Phase-2 Np-237 Oxide Conversion Line, in conjunction with the H-Canyon Frames Process to restore the H-Canyon capability to process and recover Np-237 and Pu-238 from irradiated Np-237 targets and address potential synergies with other programs like recovery of Pu-244 and heavy isotopes of curium from other target material.

  5. PLUTONIUM UPTAKE AND BEHAVIOR IN PLANTS OF THE DESERT SOUTHWEST: A PRELIMINARY ASSESSMENT

    SciTech Connect (OSTI)

    Caldwell, E.; Duff, M.; Ferguson, C.

    2011-03-01

    Eight species of desert vegetation and associated soils were collected from the Nevada National Security Site (N2S2) and analyzed for 238Pu and 239+240Pu concentrations. Amongst the plant species sampled were: atmospheric elemental accumulators (moss and lichen), the very slow growing, long-lived creosote bush and the rapidly growing, short-lived cheatgrass brome. The diversity of growth strategies provided insight into the geochemical behavior and bio-availability of Pu at the N2S2. The highest concentrations of Pu were measured in the onion moss (24.27 Bq kg-1 238Pu and 52.78 Bq kg-1 239+240Pu) followed by the rimmed navel lichen (8.18 Bq kg-1 and 18.4 Bq kg-1 respectively), pointing to the importance of eolian transport of Pu. Brome and desert globemallow accumulated between 3 and 9 times higher concentrations of Pu than creosote and sage brush species. These results support the importance of species specific elemental accumulation strategies rather than exposure duration as the dominant variable influencing Pu concentrations in these plants. Total vegetation elemental concentrations of Ce, Fe, Al, Sm and others were also analyzed. Strong correlations were observed between Fe and Pu. This supports the conclusion that Pu was accumulated as a consequence of the active accumulation of Fe and other plant required nutrients. Cerium and Pu are considered to be chemical analogs. Strong correlations observed in plants support the conclusion that these elements displayed similar geochemical behavior in the environment as it related to the biochemical uptake process of vegetation. Soils were also sampled in association with vegetation samples. This allowed for the calculation of a concentration ratio (CR). The CR values for Pu in plants were highly influenced by the heterogeneity of Pu distribution among sites. Results from the naturally occurring elements of concern were more evenly distributed between sample sites. This allowed for the development of a pattern of plant species that accumulated Ce, Sm, Fe and Al. The highest accumulators of these elements were onion moss, lichen flowed by brome. The lowest accumulators were creosote bush and fourwing saltbush. This ranked order corresponds to plant accumulations of Pu.

  6. Estimation of the formation rates of polyatomic species of heavy metals in plutonium analyses using a multicollector ICP-MS with a desolvating nebulizer

    SciTech Connect (OSTI)

    Mitroshkov, Alexandre V. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Olsen, Khris B. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Thomas, Linda M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2015-01-01

    The analyses of IAEA and environmental samples for Plutonium isotopic content are conducted normally at very low concentrations of Pu–usually in the range of part per trillion level and even more often at the parts per quadrillion level. To analyze such low concentrations, the interferences in the analytical solution must be reduced as much as possible. Polyatomic interferences (PIs), formed by the heavy metals (HMs) from Hf to Bi are known to create the problems for Pu isotopic analyses, because even the relatively high resolution of a modern multicollector ICP-MS is not enough to separate Pu isotopes from this PIs in most of the cases. Desolvating nebulizers (DSN) (e.g. APEX and AridusII) reduce significantly the formation of PIs compare to the use of wet plasma. The purpose of this work was to investigate the rate of formation of PIs, produced by HMs, when high resolution MC ICP-MS with desolvating nebulizer was used for Pu isotopic analyses and to estimate the influence of the metals present in the sample on the results of analyses. The NU Plasma HR Multicollector and AridusII desolvating nebulizer were used in this investigation. This investigation was done for all Pu isotopes normally analyzed by ICP-MS, including ²??Pu, with the exception of ²³?Pu, which most of the time can’t be analyzed by ICP-MS, because of the overwhelming presence of ²³?U in the solutions. The PI formation rates were determined and reported for all 12 HMs from Hf to Bi. Selected IAEA samples were scanned for the presence of HMs and the influence of HMs on the results of Pu isotopic analyses was evaluated. It was found that the implemented separation procedure provides sufficient separation of HM from Pu, although the effect of PIs on the measurement of low level isotopes like ²?¹Pu and ²?²Pu in some cases can still be observed.

  7. Analysis on fuel breeding capability of FBR core region based on minor actinide recycling doping

    SciTech Connect (OSTI)

    Permana, Sidik; Novitrian,; Waris, Abdul; Ismail; Suzuki, Mitsutoshi; Saito, Masaki

    2014-09-30

    Nuclear fuel breeding based on the capability of fuel conversion capability can be achieved by conversion ratio of some fertile materials into fissile materials during nuclear reaction processes such as main fissile materials of U-233, U-235, Pu-239 and Pu-241 and for fertile materials of Th-232, U-238, and Pu-240 as well as Pu-238. Minor actinide (MA) loading option which consists of neptunium, americium and curium will gives some additional contribution from converted MA into plutonium such as conversion Np-237 into Pu-238 and it's produced Pu-238 converts to Pu-239 via neutron capture. Increasing composition of Pu-238 can be used to produce fissile material of Pu-239 as additional contribution. Trans-uranium (TRU) fuel (Mixed fuel loading of MOX (U-Pu) and MA composition) and mixed oxide (MOX) fuel compositions are analyzed for comparative analysis in order to show the effect of MA to the plutonium productions in core in term of reactor criticality condition and fuel breeding capability. In the present study, neptunium (Np) nuclide is used as a representative of MAin trans-uranium (TRU) fuel composition as Np-MOX fuel type. It was loaded into the core region gives significant contribution to reduce the excess reactivity in comparing to mixed oxide (MOX) fuel and in the same time it contributes to increase nuclear fuel breeding capability of the reactor. Neptunium fuel loading scheme in FBR core region gives significant production of Pu-238 as fertile material to absorp neutrons for reducing excess reactivity and additional contribution for fuel breeding.

  8. Nordisk kernesikkerhedsforskning Norrnar kjarnryggisrannsknir

    E-Print Network [OSTI]

    in the Nordic lake sedi- ment, pore-water and lake water; (7) Sequential extraction of Pu in soil, sediment sediment, pore-water and lake water; (7) Sequential extraction of Pu in soil, sediment and concrete samples in partners labs, which in- cludes: (1) Further development on the speciation of 129I and 127I in water sam

  9. Neutron scattering studies in the actinide region. Progress report, August 1, 1992--July 31, 1993

    SciTech Connect (OSTI)

    Kegel, G.H.R.; Egan, J.J.

    1993-09-01

    This report discusses the following topics: Prompt fission neutron energy spectra for {sup 235}U and {sup 239}Pu; Two-parameter measurement of nuclear lifetimes; ``Black`` neutron detector; Data reduction techniques for neutron scattering experiments; Inelastic neutron scattering studies in {sup 197}Au; Elastic and inelastic scattering studies in {sup 239}Pu; and neutron induced defects in silicon dioxide MOS structures.

  10. First Semester Philadelphia University

    E-Print Network [OSTI]

    Groups. Classification of Subgroups of Cyclic Groups. 6 Permutation Groups: Definition and Notation/ Cole 2010. Call number in PU library: 512.02 GAL. - John B. Fraleigh, A First Course in Abstract Algebra, 7th Edition, Pearson 2003. Call number in PU library: 512.02 FRA. - Amin Witno, Group Theory

  11. SCATTERING CONFIGURATION SPACES RICHARD MELROSE AND MICHAEL SINGER

    E-Print Network [OSTI]

    Melrose, Richard

    with orners T PF foundry low up V QF sntersetionEorders II RF foundry ongurtion spes IT SF wultiEdigonls IW TF hEolletions PP UF foundry digonls PS VF ttering ongurtion spes PU WF eordering lowEups PU IHF

  12. Role of self-irradiation defects on the ageing of 239 , J.-C. Griveau1

    E-Print Network [OSTI]

    Boyer, Edmond

    and critical current density measurements, are used to study the ageing of the actinide superconductor PuCoGa5. These measurements reveal that 2-nm sized non- superconducting point-like regions are the main damage formed during. Introduction. ­ The discovery of superconductivity in PuCoGa5 [1], with characteristics intermediate between

  13. Subsurface Behavior of Plutonium and Americium at Non-Hanford Sites and Relevance to Hanford

    SciTech Connect (OSTI)

    Cantrell, Kirk J.; Riley, Robert G.

    2008-02-01

    Seven sites where Pu release to the environment has raised significant environmental concerns have been reviewed. A summary of the most significant hydrologic and geochemical features, contaminant release events and transport processes relevant to Pu migration at the seven sites is presented.

  14. Multiple Antennas in Wireless Communications: Array Signal Processing and Channel Capacity

    E-Print Network [OSTI]

    Hero, Alfred O.

    squares (LMS) algorithm known as the sequential Partial Update LMS Algorithm for adaptive beamforming. Partial update LMS (PU-LMS) algorithms are reduced complexity versions of the full update LMS that update PU-LMS, which selects the subsets at random at each iteration. We show that the new algorithm

  15. I.R.Yukhnovskii, M.V.Tokarchuk, I.P.Omelyan, R.I.Zhelem STATISTICAL THEORY FOR DIFFUSION OF

    E-Print Network [OSTI]

    multiplication factor in the system; transport of solved salts of enriched uranium 235U also increases the object and sprinkling of radioactive air by water solutions. At low points of block \\B" and ma- chine hall water are unique and hold isotopes of uranium 234U, 235U, 236U, 238U, plutonium 239Pu, 240Pu, americium 241Am

  16. Analysis of tank 39H (HTF-39-15-61, 62) surface and subsurface supernatant samples in support of corrosion control program

    SciTech Connect (OSTI)

    Oji, L. N.

    2015-08-19

    This report provides the results of analyses on Tanks 39H surface and subsurface supernatant liquid samples in support of the Corrosion Control Program. Analyses included warm acid strike preparation followed by analysis for silicon, aluminum, and sodium and water dilution preparation followed by analysis for anions. Other reported analytical results include analyses results for uranium, Pu-241 and Pu-239.

  17. Revista Iguanazul, Number 5

    E-Print Network [OSTI]

    Santopietro, Judith

    , kubanë nyooyen teky am kum käh ti mëh tuu jäts pu’x yoytyëkët. Tyeety mutuh a’të ku nyëkx tsoontaaky jäts jäm iats keshë Tuknëëmët It ma pu’x ta tëkë jäts yëk nikshë ma jäm mëh ka’p njotm. Kubanë tu’k në tni näsh kepy kiuty këxm; n’it tu’k mëh tsa...

  18. Multirecycling of Plutonium from LMFBR Blanket in Standard PWRs Loaded with MOX Fuel

    SciTech Connect (OSTI)

    Sonat Sen; Gilles Youinou

    2013-02-01

    It is now well-known that, from a physics standpoint, Pu, or even TRU (i.e. Pu+M.A.), originating from LEU fuel irradiated in PWRs can be multirecycled also in PWRs using MOX fuel. However, the degradation of the isotopic composition during irradiation necessitates using enriched U in conjunction with the MOX fuel either homogeneously or heterogeneously to maintain the Pu (or TRU) content at a level allowing safe operation of the reactor, i.e. below about 10%. The study is related to another possible utilization of the excess Pu produced in the blanket of a LMFBR, namely in a PWR(MOX). In this case the more Pu is bred in the LMFBR, the more PWR(MOX) it can sustain. The important difference between the Pu coming from the blanket of a LMFBR and that coming from a PWR(LEU) is its isotopic composition. The first one contains about 95% of fissile isotopes whereas the second one contains only about 65% of fissile isotopes. As it will be shown later, this difference allows the PWR fed by Pu from the LMFBR blanket to operate with natural U instead of enriched U when it is fed by Pu from PWR(LEU)

  19. Return on Investment from Academic Supercomputing

    E-Print Network [OSTI]

    Newby, Gregory B.

    ) on the Top 500 List Count and Publication Count (PuC), and · Model 2: Publication Count (PuC) as a function: Regression Analysis · Investment in high performance computing, as measured by entries on the Top 500 list.S. News and World Report rankings Independent variables · Top 500 List count and rank of entries o Mapped

  20. Characterization of Protein Adsorption onto Biomaterials by MALDI-TOFMS Mark E. McComb,1 Richard D. Oleschuk,1 Yves Marois,3 Martin W. King,3 Art Chow,1 Werner Ens,2

    E-Print Network [OSTI]

    Ens, Werner

    Characterization of Protein Adsorption onto Biomaterials by MALDI-TOFMS Mark E. McComb,1 Richard D Introduction Surfaces of medical devices made of polymeric biomaterials such as polyurethane (PU) are often onto membranes as a means to study single protein-biomaterial interactions.[1] Polyurethane (PU) has

  1. Impact of Fission Products Impurity on the Plutonium Content of Metal- and Oxide- Fuels in Sodium Cooled Fast Reactors

    SciTech Connect (OSTI)

    Hikaru Hiruta; Gilles Youinou

    2013-09-01

    This short report presents the neutronic analysis to evaluate the impact of fission product impurity on the Pu content of Sodium-cooled Fast Reactor (SFR) metal- and oxide- fuel fabrication. The similar work has been previously done for PWR MOX fuel [1]. The analysis will be performed based on the assumption that the separation of the fission products (FP) during the reprocessing of UOX spent nuclear fuel assemblies is not perfect and that, consequently, a certain amount of FP goes into the Pu stream used to fabricate SFR fuels. Only non-gaseous FPs have been considered (see the list of 176 isotopes considered in the calculations in Appendix 1 of Reference 1). Throughout of this report, we define the mixture of Pu and FPs as PuFP. The main objective of this analysis is to quantify the increase of the Pu content of SFR fuels necessary to maintain the same average burnup at discharge independently of the amount of FP in the Pu stream, i.e. independently of the PuFP composition. The FP losses are considered element-independent, i.e., for example, 1% of FP losses mean that 1% of all non-gaseous FP leak into the Pu stream.

  2. The solubility of hydrogen in plutonium in the temperature range 475 to 825 degrees centigrade

    SciTech Connect (OSTI)

    Allen, T.H.

    1991-01-01

    The solubility of hydrogen (H) in plutonium metal (Pu) was measured in the temperature range of 475 to 825{degree}C for unalloyed Pu (UA) and in the temperature range of 475 to 625{degree}C for Pu containing two-weight-percent gallium (TWP). For TWP metal, in the temperature range 475 to 600{degree}C, the saturated solution has a maximum hydrogen to plutonium ration (H/Pu) of 0.00998 and the standard enthalpy of formation ({Delta}H{degree}{sub f(s)}) is (-0.128 {plus minus} 0.0123) kcal/mol. The phase boundary of the solid solution in equilibrium with plutonium dihydride (PuH{sub 2}) is temperature independent. In the temperature range 475 to 625{degree}C, UA metal has a maximum solubility at H/Pu = 0.011. The phase boundary between the solid solution region and the metal+PuH{sub 2} two-phase region is temperature dependent. The solubility of hydrogen in UA metal was also measured in the temperature range 650 to 825{degree}C with {Delta}H{degree}{sub f(s)} = (-0.104 {plus minus} 0.0143) kcal/mol and {Delta}S{degree}{sub f(s)} = 0. The phase boundary is temperature dependent and the maximum hydrogen solubility has H/Pu = 0.0674 at 825{degree}C. 52 refs., 28 figs., 9 tabs.

  3. Non-destructive assay of EBR-II blanket elements using resonance transmission analysis.

    SciTech Connect (OSTI)

    Klann, R.T.; Poenitz, W.P.

    1998-09-11

    Resonance transmission analysis utilizing a faltered reactor beam was examined as a means of determining the {sup 239}Pu content in Experimental Breeder Reactor-II depleted uranium blanket elements. The technique uses cadmium and gadolinium falters along with a {sup 239}Pu fission chamber to isolate the 0.3 eV resonance in {sup 239}Pu. In the energy range of this resonance (0.1 eV to 0.5 ev), the total microscopic cross-section of {sup 239}Pu is significantly greater than the cross-sections of {sup 238}U and {sup 235}U. This large difference allows small changes in the {sup 239}Pu content of a sample to result in large changes in the mass signal response. Tests with small stacks of depleted uranium and {sup 239}Pu foils indicate a significant change in response based on the {sup 239}Pu content of the foil stack. In addition, the tests indicate good agreement between the measured and predicted values of {sup 239}Pu up to approximately two weight percent.

  4. OBES "One Pager"

    SciTech Connect (OSTI)

    Tobin, J G

    2008-11-07

    We are developing and utilizing photon dichroic and spin resolved techniques to investigate electron correlation in complex systems. These materials include potential spintronic device sources such as Fe/GaAs and f electronic materials such as non-magnetic {delta}-Pu. We are pursuing Double Polarization Photoelectron Dichroism measurements of the Fano Effect, using spin resolving detection in photoelectron spectroscopy, to test the nature of electron correlation in Pu. (See Pubs 2, 4 & 5.) If successful, we will solve the riddle of Pu electronic structure that has remained unresolved for the last 60 years. We are also developing a Bremstrahlung Isochromat Spectroscopy (BIS) capability to permit the direct measurement of the unoccupied electronic structure of Pu, which is another missing piece in the puzzle of Pu electronic structure.

  5. BAR-CODE BASED WEIGHT MEASUREMENT STATION FOR PHYSICAL INVENTORY TAKING OF PLUTONIUM OXIDE CONTAINERS AT THE MINING AND CHEMICAL COMBINE RADIOCHEMICAL REPROCESSING PLANT NEAR KRASNOYARSK, SIBERIA.

    SciTech Connect (OSTI)

    SUDA,S.

    1999-09-20

    This paper describes the technical tasks being implemented to computerize the physical inventory taking (PIT) at the Mining and Chemical Combine (Gorno-Khimichesky Kombinat, GKhK) radiochemical plant under the US/Russian cooperative nuclear material protection, control, and accounting (MPC and A) program. Under the MPC and A program, Lab-to-Lab task agreements with GKhK were negotiated that involved computerized equipment for item verification and confirmatory measurement of the Pu containers. Tasks under Phase I cover the work for demonstrating the plan and procedures for carrying out the comparison of the Pu container identification on the container with the computerized inventory records. In addition to the records validation, the verification procedures include the application of bar codes and bar coded TIDs to the Pu containers. Phase II involves the verification of the Pu content. A plan and procedures are being written for carrying out confirmatory measurements on the Pu containers.

  6. Comparison of Spectroscopic Data with Cluster Calculations of Plutonium, Plutonium Dioxide and Uranium Dioxide

    SciTech Connect (OSTI)

    Tobin, J G; Yu, S W; Chung, B W; Ryzhkov, M V; Mirmelstein, A

    2012-05-15

    Using spectroscopic data produced in the experimental investigations of bulk systems, including X-Ray Absorption Spectroscopy (XAS), Photoelectron Spectroscopy (PES) and Bremstrahlung Isochromat Spectroscopy (BIS), the theoretical results within for UO{sub 2}{sup 6}, PuO{sub 2}{sup 6} and Pu{sup 7} clusters have been evaluated. The calculations of the electronic structure of the clusters have been performed within the framework of the Relativistic Discrete-Variational Method (RDV). The comparisons between the LLNL experimental data and the Russian calculations are quite favorable. The cluster calculations may represent a new and useful avenue to address unresolved questions within the field of actinide electron structure, particularly that of Pu. Observation of the changes in the Pu electronic structure as a function of size suggests interesting implications for bulk Pu electronic structure.

  7. Delocalization and occupancy effects of 5f orbitals in plutonium intermetallics using L3-edge resonant X-ray emission spectroscopy

    SciTech Connect (OSTI)

    Booth, C. H.; Medling, S. A.; Jiang, Yu; Bauer, E. D.; Tobash, P. H.; Mitchell, J. N.; Veirs, D. K.; Wall, M. A.; Allen, P. G.; Kas, J. J.; Sokaras, D.; Nordlund, D.; Weng, T.-C.

    2014-06-24

    Although actinide (An) L3 -edge X-ray absorption near-edge structure (XANES) spectroscopy has been very effective in determining An oxidation states in insulating, ionically bonded materials, such as in certain coordination compounds and mineral systems, the technique fails in systems featuring more delocalized 5f orbitals, especially in metals. Recently, actinide L3-edge resonant X-ray emission spec- troscopy (RXES) has been shown to be an effective alternative. This technique is further demonstrated here using a parameterized partial unoccupied density of states method to quantify both occupancy and delocalization of the 5f orbital in ?-Pu, ?-Pu, PuCoGa5 , PuCoIn5 , and PuSb2. These new results, supported by FEFF calculations, highlight the effects of strong correlations on RXES spectra and the technique?s ability to differentiate between f-orbital occupation and delocalization.

  8. Next-generation purex flowsheets with acetohydroxamic acid as complexant for FBR and thermal-fuel reprocessing

    SciTech Connect (OSTI)

    Kumar, Shekhar; Koganti, S.B.

    2008-07-01

    Acetohydroxamic acid (AHA) is a novel complexant for recycle of nuclear-fuel materials. It can be used in ordinary centrifugal extractors, eliminating the need for electro-redox equipment or complex maintenance requirements in a remotely maintained hot cell. In this work, the effect of AHA on Pu(IV) distribution ratios in 30% TBP system was quantified, modeled, and integrated in SIMPSEX code. Two sets of batch experiments involving macro Pu concentrations (conducted at IGCAR) and one high-Pu flowsheet (literature) were simulated for AHA based U-Pu separation. Based on the simulation and validation results, AHA based next-generation reprocessing flowsheets are proposed for co-processing based FBR and thermal-fuel reprocessing as well as evaporator-less macro-level Pu concentration process required for MOX fuel fabrication. Utilization of AHA results in significant simplification in plant design and simpler technology implementations with significant cost savings. (authors)

  9. Mechanical environmental transport of actinides and ¹³?Cs from an arid radioactive waste disposal site

    SciTech Connect (OSTI)

    Snow, Mathew S.; Clark, Sue B.; Morrison, Samuel S.; Watrous, Matthew G.; Olson, John E.; Snyder, Darin C.

    2015-10-01

    Particulate transport represents an important mechanism for actinides and fission products at the Earth's surface; soil samples taken in the early 1970's near the Subsurface Disposal Area (SDA) at Idaho National Laboratory (INL) provide a case study for examining the mechanisms and characteristics of actinide transport under arid conditions. Transuranic waste was disposed via shallow land burial at the SDA until shortly after a flooding event that occurred in 1969. In this study we analyze soils collected in the early 1970's for ¹³?Cs, ²?¹Am, and Pu using a combination of radiometric and mass spectrometric techniques. Two distinct ²??Pu/²³?Pu isotopic ratios are observed for contamination from the SDA, with values ranging from at least 0.059 to 0.069. ²?¹Am concentrations are observed to increase only slightly in 0-4 cm soils over the ~40 year period since soil sampling, contrary to Markham's previous hypothesis that ²?¹Pu is principally associated with the 0-4 cm soil fractions (Markham 1978). The lack of statistical difference in ²?¹Am/²³??²??Pu ratios with depth suggests mechanical transport and mixing discrete contaminated particles under arid conditions. Occasional samples beyond the northeastern corner are observed to contain anomalously high Pu concentrations with corresponding low ²??Pu/²³?Pu atoms ratios, suggesting the occurrence of "hot particles;" application of a background Pu subtraction results in calculated Pu atom ratios for the "hot particles" which are statistically similar to those observed in the northeastern corner. Taken together, our data suggests that flooding resulted in mechanical transport of contaminated particles into the area between the SDA and the flood containment dike in the northeastern corner, following which subsequent contamination spreading resulted from wind transport of discrete particles.

  10. Mechanical environmental transport of actinides and ¹³?Cs from an arid radioactive waste disposal site

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Snow, Mathew S.; Clark, Sue B.; Morrison, Samuel S.; Watrous, Matthew G.; Olson, John E.; Snyder, Darin C.

    2015-10-01

    Particulate transport represents an important mechanism for actinides and fission products at the Earth's surface; soil samples taken in the early 1970's near the Subsurface Disposal Area (SDA) at Idaho National Laboratory (INL) provide a case study for examining the mechanisms and characteristics of actinide transport under arid conditions. Transuranic waste was disposed via shallow land burial at the SDA until shortly after a flooding event that occurred in 1969. In this study we analyze soils collected in the early 1970's for ¹³?Cs, ²?¹Am, and Pu using a combination of radiometric and mass spectrometric techniques. Two distinct ²??Pu/²³?Pu isotopic ratiosmore »are observed for contamination from the SDA, with values ranging from at least 0.059 to 0.069. ²?¹Am concentrations are observed to increase only slightly in 0-4 cm soils over the ~40 year period since soil sampling, contrary to Markham's previous hypothesis that ²?¹Pu is principally associated with the 0-4 cm soil fractions (Markham 1978). The lack of statistical difference in ²?¹Am/²³??²??Pu ratios with depth suggests mechanical transport and mixing discrete contaminated particles under arid conditions. Occasional samples beyond the northeastern corner are observed to contain anomalously high Pu concentrations with corresponding low ²??Pu/²³?Pu atoms ratios, suggesting the occurrence of "hot particles;" application of a background Pu subtraction results in calculated Pu atom ratios for the "hot particles" which are statistically similar to those observed in the northeastern corner. Taken together, our data suggests that flooding resulted in mechanical transport of contaminated particles into the area between the SDA and the flood containment dike in the northeastern corner, following which subsequent contamination spreading resulted from wind transport of discrete particles.« less

  11. LITERATURE REVIEW OF PUO2 CALCINATION TIME AND TEMPERATURE DATA FOR SPECIFIC SURFACE AREA

    SciTech Connect (OSTI)

    Daniel, G.

    2012-03-06

    The literature has been reviewed in December 2011 for calcination data of plutonium oxide (PuO{sub 2}) from plutonium oxalate Pu(C{sub 2}O{sub 4}){sub 2} precipitation with respect to the PuO{sub 2} specific surface area (SSA). A summary of the literature is presented for what are believed to be the dominant factors influencing SSA, the calcination temperature and time. The PuO{sub 2} from Pu(C{sub 2}O{sub 4}){sub 2} calcination data from this review has been regressed to better understand the influence of calcination temperature and time on SSA. Based on this literature review data set, calcination temperature has a bigger impact on SSA versus time. However, there is still some variance in this data set that may be reflecting differences in the plutonium oxalate preparation or different calcination techniques. It is evident from this review that additional calcination temperature and time data for PuO{sub 2} from Pu(C{sub 2}O{sub 4}){sub 2} needs to be collected and evaluated to better define the relationship. The existing data set has a lot of calcination times that are about 2 hours and therefore may be underestimating the impact of heating time on SSA. SRNL recommends that more calcination temperature and time data for PuO{sub 2} from Pu(C{sub 2}O{sub 4}){sub 2} be collected and this literature review data set be augmented to better refine the relationship between PuO{sub 2} SSA and its calcination parameters.

  12. LAB-SCALE DEMONSTRATION OF PLUTONIUM PURIFICATION BY ANION EXCHANGE, PLUTONIUM (IV) OXALATE PRECIPITATION, AND CALCINATION TO PLUTONIUM OXIDE TO SUPPORT THE MOX FEED MISSION

    SciTech Connect (OSTI)

    Crowder, M.; Pierce, R.

    2012-08-22

    H-Canyon and HB-Line are tasked with the production of PuO{sub 2} from a feed of plutonium metal. The PuO{sub 2} will provide feed material for the MOX Fuel Fabrication Facility. After dissolution of the Pu metal in H-Canyon, the solution will be transferred to HB-Line for purification by anion exchange. Subsequent unit operations include Pu(IV) oxalate precipitation, filtration and calcination to form PuO{sub 2}. This report details the results from SRNL anion exchange, precipitation, filtration, calcination, and characterization tests, as requested by HB-Line1 and described in the task plan. This study involved an 80-g batch of Pu and employed test conditions prototypical of HB-Line conditions, wherever feasible. In addition, this study integrated lessons learned from earlier anion exchange and precipitation and calcination studies. H-Area Engineering selected direct strike Pu(IV) oxalate precipitation to produce a more dense PuO{sub 2} product than expected from Pu(III) oxalate precipitation. One benefit of the Pu(IV) approach is that it eliminates the need for reduction by ascorbic acid. The proposed HB-Line precipitation process involves a digestion time of 5 minutes after the time (44 min) required for oxalic acid addition. These were the conditions during HB-line production of neptunium oxide (NpO{sub 2}). In addition, a series of small Pu(IV) oxalate precipitation tests with different digestion times were conducted to better understand the effect of digestion time on particle size, filtration efficiency and other factors. To test the recommended process conditions, researchers performed two nearly-identical larger-scale precipitation and calcination tests. The calcined batches of PuO{sub 2} were characterized for density, specific surface area (SSA), particle size, moisture content, and impurities. Because the 3013 Standard requires that the calcination (or stabilization) process eliminate organics, characterization of PuO{sub 2} batches monitored the presence of oxalate by thermogravimetric analysis-mass spectrometry (TGA-MS). To use the TGA-MS for carbon or oxalate content, some method development will be required. However, the TGA-MS is already used for moisture measurements. Therefore, SRNL initiated method development for the TGA-MS to allow quantification of oxalate or total carbon. That work continues at this time and is not yet ready for use in this study. However, the collected test data can be reviewed later as those analysis tools are available.

  13. 46 I E E E S O F T WA R E Pu b l i s h e d b y t h e I EEE C o m p u t e r S o c i e t y 0 74 0 -74 5 9 / 10 / $ 2 6 . 0 0 2 0 10 I E E E modeling tools) or tools for visual understanding of

    E-Print Network [OSTI]

    Telea, Alexandru C.

    of a software product's total life-cycle costs, and 40 percent of that cost is software understand- ing.2,3 Nor of an existing architecture. Visual understanding tools aim to support sev- eral tasks, such as comparing desired and actual architectures, identifying architecture violations, highlighting architectural patterns or layers

  14. Separation Of Uranium And Plutonium Isotopes For Measurement By Multi Collector Inductively Coupled Plasma Mass Spectroscopy

    SciTech Connect (OSTI)

    Martinelli, R E; Hamilton, T F; Williams, R W; Kehl, S R

    2009-03-29

    Uranium (U) and plutonium (Pu) isotopes in coral soils, contaminated by nuclear weapons testing in the northern Marshall Islands, were isolated by ion-exchange chromatography and analyzed by mass spectrometry. The soil samples were spiked with {sup 233}U and {sup 242}Pu tracers, dissolved in minerals acids, and U and Pu isotopes isolated and purified on commercially available ion-exchange columns. The ion-exchange technique employed a TEVA{reg_sign} column coupled to a UTEVA{reg_sign} column. U and Pu isotope fractions were then further isolated using separate elution schemes, and the purified fractions containing U and Pu isotopes analyzed sequentially using multi-collector inductively coupled plasma mass spectrometer (MCICP-MS). High precision measurements of {sup 234}U/{sup 235}U, {sup 238}U/{sup 235}U, {sup 236}U/{sup 235}U, and {sup 240}Pu/{sup 239}Pu in soil samples were attained using the described methodology and instrumentation, and provide a basis for conducting more detailed assessments of the behavior and transfer of uranium and plutonium in the environment.

  15. Dust transport: Wind blown and mechanical resuspension, July 1983 to December 1984

    SciTech Connect (OSTI)

    Langer, G.

    1986-09-20

    This study defines the processes that resuspend plutonium (Pu) particles from Pu-contaminated soil at Rocky Flats. Such knowledge can predict the transport of Pu particles from the site and the population dose. A vertical dust flux tower profiled the plume of Pu particles from the site. The data show a 70% reduction between 1 and 10 m in the concentration of coarse and inhalable Pu particles. The respirable particle concentration remained steady at both heights, slightly above background levels. High winds visually resuspend large amounts of dust for short periods, but we suspected that present sampling devices do not function properly above 50 km/h. During a windstorm reaching 80 km/h, the size-selective sampler used seriously underestimated the dust(Pu) concentration. Wind tunnel studies measured resuspension versus wind speed from our prairie grass covered, arid soil. We failed to find a good correlation between resuspension and wind speed. This led to a search for alternative mechanisms of resuspension besides wind erosion. Resuspension of dust(Pu) from grass proved to be important, as well as resuspension from rain splash.

  16. Properties of Liquid Plutonium

    SciTech Connect (OSTI)

    Freibert, Franz J.; Mitchell, Jeremy N.; Schwartz, Daniel S.; Saleh, Tarik A.; Migliori, Albert

    2012-08-02

    Unalloyed polycrystalline Pu displays extreme thermal expansion behavior, i.e., {alpha} {yields} {beta} {yields} {gamma} {yields} {delta} increases by 25% in volume and {delta} {yields} {var_epsilon} {yields} liquid decreases by 4.5% in volume. Thus, making it difficult to measure density into the liquid state. Dilatometer outfitted with CaF molten metal cell offers a proven capability to measure thermal expansion in molten metals, but has yet to be proven for Pu. Historic data from the liquid nuclear fuels program will prove extremely useful as a guide to future measurements. 3.3at% Ga changes Pu molten metal properties: 50% increase in viscosity and {approx}3% decrease in density. Fe may decrease the density by a small amount assuming an averaging of densities for Pu-Ga and Pu-Fe liquids. More recent Boivineau (2009) work needs some interpretation, but technique is being employed in (U,Pu)O{sub 2} nuclear fuels program (Pu Futures, 2012).

  17. High-level assessment of LANL ABC Design

    SciTech Connect (OSTI)

    Not Available

    1994-04-15

    An annual weapon`s grade Pu disposition goal should be stated and related to the amount of Pu that needs to be disposed of. It needs to be determined to what extent it is possible to destroy Pu without building up any new Pu, i.e., how realistic this goal is. The strong positive Doppler coefficient for a Pu core might require the addition of some fertile material to ensure a negative Doppler coefficient. This in turn will affect the net Pu disposition rate. If a fertile material is required throughout the life of the ABC to ensure a negative Doppler coefficient, the difference between the molten salt ABC and other reactors in regard to Pu disposition is not a principled difference anymore but one of degree. A rationale has then to be developed that explains why {open_quotes}x{close_quotes} kg production of fissile material are acceptable but {open_quotes}y{close_quotes} kg are not. It is important to determine how a requirement for electricity production will impact on the ABC design choices. It is conceivable that DOE will not insist on electricity generation. In this case advantage has to be taken in terms of design simplifications and relaxed operating conditions.

  18. Results of the Excreta Bioassay Quality Control Program for April 1, 2009 through March 31, 2010

    SciTech Connect (OSTI)

    Antonio, Cheryl L.

    2012-07-19

    A total of 58 urine samples and 10 fecal samples were submitted during the report period (April 1, 2009 through March 31, 2010) to General Engineering Laboratories, South Carolina by the Hanford Internal Dosimetry Program (IDP) to check the accuracy, precision, and detection levels of their analyses. Urine analyses for Sr, 238Pu, 239Pu, 241Am, 243Am 235U, 238U, elemental uranium and fecal analyses for 241Am, 238Pu and 239Pu were tested this year as well as four tissue samples for 238Pu, 239Pu, 241Am and 241Pu. The number of QC urine samples submitted during the report period represented 1.3% of the total samples submitted. In addition to the samples provided by IDP, GEL was also required to conduct their own QC program, and submit the results of analyses to IDP. About 33% of the analyses processed by GEL during the third year of this contract were quality control samples. GEL tested the performance of 21 radioisotopes, all of which met or exceeded the specifications in the Statement of Work within statistical uncertainty (Table 4).

  19. The Optimum Plutonium Inert Matrix Fuel Form for Reactor-Based Plutonium Disposition

    SciTech Connect (OSTI)

    Tulenko, J.S.; Wang, J.; Acosta, C.

    2004-10-06

    The University of Florida has underway an ongoing research program to validate the economic, operational and performance benefits of developing an inert matrix fuel (IMF) for the disposition of the U.S. weapons plutonium (Pu) and for the recycle of reprocessed Pu. The current fuel form of choice for Pu disposition for the Department of Energy is as a mixed oxide (MOX) (PuO2/UO2). We will show analyses that demonstrate that a Silicon Carbide (SiC) IMF offers improved performance capabilities as a fuel form for Pu recycle and disposition. The reason that UF is reviewing various materials to serve as an inert matrix fuel is that an IMF fuel form can offer greatly reduced Pu and transuranic isotope (TRU) production and also improved thermal performance characteristics. Our studies showed that the Pu content is reduced by an order of magnitude while centerline fuel temperatures are reduced approximately 380 degrees centigrade compared to MOX. These reduced temperatures result in reduced stored heat and thermal stresses in the pellet. The reduced stored heat reduces the consequences of the loss of coolant accident, while the reduced temperatures and thermal stresses yield greatly improved fuel performance. Silicon Carbide is not new to the nuclear industry, being a basic fuel material in gas cooled reactors.

  20. The Optimum Plutonium Inert Matrix Fuel Form for Reactor-Based Plutonium Disposition

    SciTech Connect (OSTI)

    Tulenko, J.S.; Wang, J.; Acosta, C.

    2004-10-03

    The University of Florida has underway an ongoing research program to validate the economic, operational and performance benefits of developing an inert matrix fuel (IMF) for the disposition of the U.S. weapons plutonium (Pu) and for the recycle of reprocessed Pu. The current fuel form of choice for Pu disposition for the Department of Energy is as a mixed oxide (MOX) (PuO2/UO2). We will show analyses that demonstrate that a Silicon Carbide (SiC) IMF offers improved performance capabilities as a fuel form for Pu recycle and disposition. The reason that UF is reviewing various materials to serve as an inert matrix fuel is that an IMF fuel form can offer greatly reduced Pu and transuranic isotope (TRU) production and also improved thermal performance characteristics. Our studies showed that the Pu content is reduced by an order of magnitude while centerline fuel temperatures are reduced approximately 380 degrees centigrade compared to MOX. These reduced temperatures result in reduced stored heat and thermal stresses in the pellet. The reduced stored heat reduces the consequences of the loss of coolant accident, while the reduced temperatures and thermal stresses yield greatly improved fuel performance. Silicon Carbide is not new to the nuclear industry, being a basic fuel material in gas cooled reactors.

  1. Plutonium and americium behavior in coral atoll environments

    SciTech Connect (OSTI)

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

    1984-02-01

    Inventories of /sup 239 +240/Pu and /sup 241/Am greatly in excess of global fallout levels persist in the benthic environments of Bikini and Enewetak Atolls. Quantities of /sup 239 +240/Pu and lesser amounts of /sup 241/Am are continuously mobilizing from these sedimentary reservoirs. The amount of /sup 239 +240/Pu mobilized to solution at any time represents 0.08 to 0.09% of the sediment inventories to a depth of 16 cm. The mobilized /sup 239 +240/Pu has solute-like characteristics and different valence states coexist in solution - the largest fraction of the soluble plutonium is in an oxidized form (+V,VI). The adsorption of plutonium to sediments is not completely reversible because of changes that occur in the relative amounts of the mixed oxidation states in solution with time. Further, any characteristics of /sup 239 +240/Pu described at one location may not necessarily be relevant in describing its behavior elsewhere following mobilization and migration. The relative amounts of /sup 241/Am to /sup 239 +240/Pu in the sedimentary deposits at Enewetak and Bikini may be altered in future years because of mobilization and radiological decay. Mobilization of /sup 239 +240/Pu is not a process unique to these atolls, and quantities in solution derived from sedimentary deposits can be found at other global sites. These studies in the equatorial Pacific have significance in assessing the long-term behavior of the transuranics in any marine environment. 22 references, 1 figure, 13 tables.

  2. Final Report for Plutonium and Quantum Criticality LDRD 03-ERD-077

    SciTech Connect (OSTI)

    Fluss, M J; McCall, S K; Chung, B W; Chapline, G F; Jackson, D D; Heffner, R H; Haire, R G

    2008-02-11

    Plutonium possesses the most complicated phase diagram in the periodic table, driven by the complexities of overlapping 5f electron orbitals. Despite the importance of the 5f electrons in defining the structure and physical properties, there is no experimental evidence that these electrons localize to form magnetic moments in pure Pu and the {sup +}{mu}SR measurements included here place an upper limit of <0.001{micro}{sub B} for the magnetic moment on Pu. Instead, a large temperature independent Pauli susceptibility indicates they form narrow conduction bands. Radiation damage from the {alpha}-particle decay of Pu creates numerous defects in the crystal structure which produce a significant temperature dependent magnetic susceptibility {chi}(T), in {alpha}-Pu, {delta}-Pu(4.3at%Ga), and Pu{sub 1-x}Am{sub x} alloys ({delta}-Pu phase). This effect can be removed by thermal annealing above room temperature. By contrast, below 35K the radiation damage is frozen in place permitting the evolution in {chi}(T) with increasing damage to be studied systematically. This leads to a two component model consisting of a Curie-Weiss term and a short-ranged interaction term consistent with disorder induced local moment models. Thus it is shown that self-damage creates localized magnetic moments in previously nonmagnetic plutonium. This effect is greatly magnified in some Pu{sub 1-x}Am{sub x} alloys where an apparent damage-induced phase transition occurs at low temperatures near Stage I annealing which results local moments on the order of 1 {micro}{sub B}/Pu. The phase is metastable, and anneals away at higher temperatures.

  3. Global plutonium management: A security option

    SciTech Connect (OSTI)

    Sylvester, K.W.B.

    1998-12-31

    The US surplus plutonium disposition program was created to reduce the proliferation risk posed by the fissile material from thousands of retired nuclear weapons. The Department of Energy has decided to process its Put into a form as secure as Pu in civilian spent fuel. While implementation issues have been considered, a major one (Russian reciprocity) remains unresolved. Russia has made disposition action conditional on extracting the fuel value of its Pu but lacks the infrastructure to do so. Assistance in the construction of the required facilities would conflict with official US policy opposing the development of a Pu fuel cycle. The resulting stagnation provides impetus for a reevaluation of US nonproliferation objectives and Pu disposition options. A strategy for satisfying Russian fuel value concerns and reducing the proliferation risk posed by surplus weapons-grade plutonium (WGPu) is proposed. The effectiveness of material alteration (e.g., isotopic, chemical, etc.{hor_ellipsis}) at reducing the desire, ability and opportunity for proliferation is assessed. Virtually all the security benefits attainable by material processing can be obtained by immobilizing Pu in large unit size/mass monoliths without a radiation barrier. Russia would be allowed to extract the Pu at a future date for use as fuel in a verifiable manner. Remote tracking capability, if proven feasible, would further improve safeguarding capability. As an alternate approach, the US could compensate Russia for its Pu, allowing it to be disposed of or processed elsewhere. A market based method for pricing Pu is proposed. Surplus Pu could represent access to nuclear fuel at a fixed price at a future date. This position can be replicated in the uranium market and priced using derivative theory. The proposed strategy attempts to meet nonproliferation objectives by recognizing technical limitations and satisfying political constraints.

  4. Preconceptual Feasibility Study to Evaluate Alternative Means to Produce Plutonium-238

    SciTech Connect (OSTI)

    John D. Bess; Matthew S. Everson

    2013-02-01

    There is currently no large-scale production of 238Pu in the United States. Feasibility studies were performed at the Idaho National Laboratory to assess the capability of developing alternative 238Pu production strategies. Initial investigations indicate potential capability to provision radioisotope-powered systems for future space exploration endeavors. For the short term production of 238Pu, sealed canisters of dilute 237Np solution in nitric acid could be irradiated in the Advanced Test Reactor (ATR). Targets in the large and medium “I” positions of the ATR were irradiated over a simulated period of 306 days and analyzed using MCNP5 and ORIGEN2.2. Approximately 0.5 kg of 238Pu could be produced annually in the ATR with purity greater than 92%. Optimization of the irradiation cycles could further increase the purity to greater than 98%. Whereas the typical purity of space batteries is between 80 to 85%, the higher purity 238Pu produced in the ATR could be blended with existing lower-purity inventory to produce useable material. Development of irradiation methods in the ATR provides the fastest alterative to restart United States 238Pu production. The analysis of 238Pu production in the ATR provides the technical basis for production using TRIGA® (Training, Research, Isotopes, General Atomics) nuclear reactors. Preliminary analyses envisage a production rate of approximately 0.7 kg annually using a single dedicated 5-MW TRIGA reactor with continuous flow loops to achieve high purity product. Two TRIGA reactors represent a robust means of providing at over 1 kg/yr of 238Pu annually using dilute solution targets of 237Np in nitric acid. Further collaboration and optimization of reactor design, radiochemical methods, and systems analyses would further increase annual 238Pu throughput, while reducing the currently evaluated reactor requirements.

  5. Discovery of plutonium-based superconductivity

    SciTech Connect (OSTI)

    Sarrao, John L.,; Thompson, J. D. (Joe David); Moreno, N. O.; Morales, L. A. (Luis A.); Wastin, F. (Franck); Rebizant, J.; Boulet, P.; Colineau, E.; Lander, G. H.

    2002-01-01

    The discovery of superconductivity in single crystals of PuCoGa{sub 5} with transition temperature T{sub c}=18.5 K is discussed. The existing data lead to the speculation that the superconductivity in PuCoGa{sub 5} may be unconventional. In such a scenario the properties of PuCoGa{sub 5} would be intermediate between those of isostructural UCoGa{sub 5} and CeCoIn{sub 5}, more heavily studied f-electron materials.

  6. Plutonium Uptake By Brucite And Hydroxylated Periclase

    SciTech Connect (OSTI)

    Farr, J.D.; Neu, M.P.; Schulze, R.K.; Honeyman, B.D.

    2009-06-02

    Batch adsorption experiments and spectroscopic investigations consistently show that aqueous Pu(IV) is quickly removed from solution and becomes incorporated in a brucite or hydroxylated MgO surface to a depth of at least 50 nm, primarily as Pu(IV) within a pH range of 8.5--12.5, and is unaffected by the presence of the organic ligand, citrate. X-ray photoelectron spectroscopy (XPS), X-ray absorption fine structure (XAFS) and Rutherford backscattering spectroscopy (RBS) were used to estimate Pu penetration depth and provide information about its chemical state.

  7. Radionuclide concentrations in honey bees from Area G at TA-54 during 1997. Progress report

    SciTech Connect (OSTI)

    Haarmann, T.K.; Fresquez, P.R.

    1998-07-01

    Honey bees were collected from two colonies located at Los Alamos National Laboratory`s Area G, Technical Area 54, and from one control (background) colony located near Jamez Springs, NM. Samples were analyzed for the following: cesium ({sup 137}Cs), americium ({sup 241}Am), plutonium ({sup 238}Pu and {sup 239,240}Pu), tritium ({sup 3}H), total uranium, and gross gamma activity. Area G sample results from both colonies were higher than the upper (95%) level background concentration for {sup 238}Pu and {sup 3}H.

  8. Mucrobial Stabilization of Plutonium in the Subsurface Environment

    SciTech Connect (OSTI)

    BJ Honeyman, AJ Francis, CJ Dodge, JB Gillow, PH Santschi

    2004-06-01

    This report outlines the results of work performed at the Colorado School of Mines, Brookhaven National Laboratory and Texas A and M University during the second reporting phase of this project. The sub-projects focused on this year include: (1) Biotransformation of Pu-contaminated soil; (2) Environmental colloids at the Rocky Flats Environmental Technology Site; (3) Production, isolation and characterization of EPS (exopolymeric substances, or exopolysaccharides); (4) Colloid trapping; (5) Determination of stability constants of complexes of Pu(IV) with organic ligands; and (6) The role of bacterial EPS in the transport of Pu through saturated porous media.

  9. Plutonium in human urine: Normal levels in the US public. 1991 Annual report, Volume 2

    SciTech Connect (OSTI)

    Wrenn, M.E.; Singh, N.P.; Xue, Ying-Hua

    1997-03-01

    A neutron induced fission track method was successfully developed for assaying {sup 239}Pu in human urine with a detection limit below 20 aCi/sample. The technique involves the co-precipitation of {sup 239}Pu with rhodizonic acid, separation of {sup 239}Pu from potentially interfering natural uranium and other inorganic materials by ion-exchange techniques, collection of the sample onto lexan detectors, irradiation of sample in MIT reactor at a fluence of 1.1 x 10{sup 17} n/cm{sup 2}, etching of the lexan slide and counting the track either manually or by some automated counting system.

  10. Seaborg's Plutonium ?

    E-Print Network [OSTI]

    Norman, Eric B; Telhami, Kristina E

    2014-01-01

    Passive x-ray and gamma-ray analysis was performed on UC Berkeley's EH&S Sample S338. The object was found to contain Pu-239 and no other radioactive isotopes. The mass of Pu-239 contained in this object was determined to be 2.0 +- 0.3 micrograms. These observations are consistent with the identification of this object being the 2.77-microgram plutonium oxide sample described by Glenn Seaborg and his collaborators as the first sample of Pu-239 that was large enough to be weighed.

  11. Seaborg's Plutonium?

    E-Print Network [OSTI]

    Eric B. Norman; Keenan J. Thomas; Kristina E. Telhami

    2015-02-17

    Passive x-ray and gamma-ray analysis was performed on UC Berkeley's EH&S Sample S338. The object was found to contain Pu-239 and no other radioactive isotopes. The mass of Pu-239 contained in this object was determined to be 2.0 +- 0.3 micrograms. These observations are consistent with the identification of this object being the 2.77-microgram plutonium oxide sample described by Glenn Seaborg and his collaborators as the first sample of Pu-239 that was large enough to be weighed.

  12. Preliminary results on the hydrolysis and carbonate complexation of dioxoplutonium(V)

    SciTech Connect (OSTI)

    Bennett, D.A.; Hoffman, D.C.; Nitsche, H.; Silva, R.J.

    1987-11-01

    The hydrolysis and carbonate complexation reactions of dioxoplutonium (V) were studied in near neutral aqueous systems. These experiments involved the addition of hydroxide or carbonate to Pu(V) in a perchorate medium. Change in the electronic adsorption spectra provided information about the chemical properties of Pu(V). The results indicate the Pu(V) does not hydrolyze below pH 7.15. In the carbonate complexation studies, log {beta}{sub 11} was measured to be 4.4 +- 0.7. 5 figs., 3 tabs.

  13. Numerical calculation of reflected and transmitted radiance in a plane parallel atmosphere by doubling very thin layers 

    E-Print Network [OSTI]

    Entrekin, Robert David

    1976-01-01

    of reciprocity (Chandrasekhar, 1960). To demonstrate how these proofs proceed, 29 equation (64) will be proved. The remaining three relations follow very similarly. The formula for a general element of r is -1 N r. . = (4 - 26 g 6. ku. Sk. = 4 - 26+ u Si... this formula, the functions p(u, u';k4) must be obtained from the table of p(cos 8). Since the points p(u, u';ki) will not generally coincide with any particular p(cos 8 ), an interpolation method will have to be used. First, p(u, u';kg) must be put...

  14. Alternating layers of plutonium and lead or indium as surrogate for plutonium

    SciTech Connect (OSTI)

    Rudin, Sven Peter

    2009-01-01

    Elemental plutonium (Pu) assumes more crystal structures than other elements, plausibly due to bonding f electrons becoming non-bonding. Complex geometries hamper understanding of the transition in Pu, but calculations predict this transition in a system with simpler geometry: alternating layers either of plutonium and lead or of plutonium and indium. Here the transition occurs via a pairing-up of atoms within Pu layers. Calculations stepping through this pairing-up reveal valuable details of the transition, for example that the transition from bonding to non-bonding proceeds smoothly.

  15. Molecular Interactions of Plutonium(VI) with Synthetic Manganese-Substituted Goethite

    E-Print Network [OSTI]

    Hu, Yung-Jin

    2011-01-01

    observed in the past for the uranyl moiety [40]. For the MSin previous studies with uranyl [40]. The Pu-O a path fitsin the literature [41] for uranyl and have been assigned as

  16. Using magnetization measurements to detect small amounts of plutonium hydride formation in plutonium metal

    SciTech Connect (OSTI)

    Kim, Jae Wook [Rutgers Univ., New Brunswick, NJ (United States); Mielke, Charles H. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Zapf, Vivien [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Baiardo, Joseph P. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Mitchell, Jeremy N. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Richmond, Scott [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Schwartz, Daniel S. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Mun, Eun D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Smith, Alice Iulia [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2014-10-20

    We report the formation of plutonium hydride in 2 at % Ga-stabilized ?-Pu, with 1 atomic % H charging. We show that magnetization measurements are a sensitive, quantitative measure of ferromagnetic plutonium hydride against the nonmagnetic background of plutonium. It was previously shown that at low hydrogen concentrations, hydrogen forms super-abundant vacancy complexes with plutonium, resulting in a bulk lattice contraction. Here we use magnetization, X-ray and neutron diffraction measurements to show that in addition to forming vacancy complexes, at least 30% of the H atoms bond with Pu to precipitate PuHx, largely on the surface of the sample with x ~ 1.9. We observe magnetic hysteresis loops below 40 K with magnetic remanence, consistent with precipitates of ferromagnetic PuH1.9.

  17. Groupement de service Graphisme : CNRS, service communication, LRF

    E-Print Network [OSTI]

    van Tiggelen, Bart

    Timashov - Fotolia « J'ai suivi les formations Datacentre organisées par EcoInfo en 2012 et 2014, j'ai pu équipements informatiques salles informatiques, datacentres analyse de cyle de vie déchets électroniques

  18. DO EIEA-0841 ENVIRONMENTAL ASSESSMENT OF THE IMPORT OF RUSSIAN

    Energy Savers [EERE]

    of the chemical form (dioxide), reducing its mobility in the environment, if released q Low gamma-radiation level and acceptable neutron emission level The Pu-238 fuel form...

  19. Why is weapons grade plutonium more hazardous to work with than highly enriched uranium?

    SciTech Connect (OSTI)

    Cournoyer, Michael E.; Costigan, Stephen A.; Schake, Bradley S.

    2015-08-01

    Highly Enriched Uranium and Weapons grade plutonium have assumed positions of dominant importance among the actinide elements because of their successful uses as explosive ingredients in nuclear weapons and the place they hold as key materials in the development of industrial use of nuclear power. While most chemists are familiar with the practical interest concerning HEU and WG Pu, fewer know the subtleties among their hazards. In this study, a primer is provided regarding the hazards associated with working with HEU and WG Pu metals and oxides. The care that must be taken to safely handle these materials is emphasized and the extent of the hazards is described. The controls needed to work with HEU and WG Pu metals and oxides are differentiated. Given the choice, one would rather work with HEU metal and oxides than WG Pu metal and oxides.

  20. Pour obtenir le grade de DOCTEUR DE L'UNIVERSIT DE GRENOBLE

    E-Print Network [OSTI]

    Paris-Sud XI, Université de

    intégrée. Parmi eux, notre cher Hervé ACHARD, qui a su assurer la partie filière de notre projet. Merci rencontre très prolifique où j'ai pu me faire de nombreux amis et collaborateurs tels que Jean-Pierre

  1. APOLLO PROGRAM LUNAR SURFACE EQUIPMENT STATUS

    E-Print Network [OSTI]

    Rathbun, Julie A.

    , 1972 17 Dec. 7, 1972 Dec. 12 1 1972 TIME- HISTORY PROPORTION OF FULL CAPABILITY OF INSTRUMENT PASSIVE_A_T_A__o_u_T_Pu_T_·-~~%~-~~~~~L_________ HOUSEKEEPIN

  2. Molten salt fuels with high plutonium solubility

    DOE Patents [OSTI]

    Moir, Ralph W; Turchi, Patrice E.A.; Shaw, Henry F; Kaufman, Larry

    2013-08-13

    The present invention includes a composition of LiF--ThF.sub.4--UF.sub.4--PuF.sub.3 for use as a fuel in a nuclear engine.

  3. RACSAMRev. R. Acad. Cien. Serie A. Mat. VOL. 97 (3), 2003, pp. 455460

    E-Print Network [OSTI]

    Díaz Díaz, Gregorio

    ­Laplaciano Resumen. En esta nota estimamos la tasa maxima de crecimiento en la frontera de las soluciones de]), it is the limit case of the p­ Lapla- cian operator pu . = div |u|p-2 u . There exist several justifying

  4. Nutrition and Alzheimer's Disease: The Role of Folate and Vitamin B

    E-Print Network [OSTI]

    Edmonds, Zachary V.

    1999-01-01

    Karlinsky H. Folate, vitamin B12 and cognitive impairment inH, Surron L, Ueland PU. Folate, vitamin B12, and serum totalBottiglieri T. Folate, vitamin B12, and neuropyschiatric

  5. Why is weapons grade plutonium more hazardous to work with than highly enriched uranium?

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Cournoyer, Michael E.; Costigan, Stephen A.; Schake, Bradley S.

    2015-08-01

    Highly Enriched Uranium and Weapons grade plutonium have assumed positions of dominant importance among the actinide elements because of their successful uses as explosive ingredients in nuclear weapons and the place they hold as key materials in the development of industrial use of nuclear power. While most chemists are familiar with the practical interest concerning HEU and WG Pu, fewer know the subtleties among their hazards. In this study, a primer is provided regarding the hazards associated with working with HEU and WG Pu metals and oxides. The care that must be taken to safely handle these materials is emphasizedmore »and the extent of the hazards is described. The controls needed to work with HEU and WG Pu metals and oxides are differentiated. Given the choice, one would rather work with HEU metal and oxides than WG Pu metal and oxides.« less

  6. ARTICLE doi:10.1038/nature10423 Deep sequencing reveals 50 novel genes

    E-Print Network [OSTI]

    Cai, Long

    Zecha3 , Marzieh Mohseni1 , Lucia Pu¨ttmann3 , Leyla Nouri Vahid1 , Corinna Jensen3 , Lia Abbasi Moheb1,3 , Melanie Bienek3 , Farzaneh Larti1 , Ines Mueller3 , Robert Weissmann3 , Hossein Darvish1 , Klaus Wrogemann

  7. Fusion-breeder program

    SciTech Connect (OSTI)

    Moir, R.W.

    1982-11-19

    The various approaches to a combined fusion-fission reactor for the purpose of breeding /sup 239/Pu and /sup 233/U are described. Design aspects and cost estimates for fuel production and electricity generation are discussed. (MOW)

  8. The Role of Colloids in the Transport of Plutonium and Americium: Implications for

    SciTech Connect (OSTI)

    Kersting, A B

    2003-09-17

    Colloids are small particulates (ranging in size from 1 to 0.001 micron) composed of inorganic and organic material and found in all natural water. Due to their small size, they have the ability to remain suspended in water and transported. Small amounts of plutonium (Pu) and americium (Am) can adsorb (attach) to colloids, and/or form colloidal-sized polymers and migrate in water. At Rocky Flats Environmental Technology Site (RFETS) sedimentation and resuspension of particulates and colloids in surface waters represent the dominant process for Pu and Am migration. The amount of Pu and Am that can be transported at RFETS has been quantified in the Pathway Analysis Report. The Pathway Analysis Report shows that the two dominant pathways for Pu and Am transport at RFETS are air and surface water. Shallow groundwater and biological pathways are minor.

  9. Analysis of resuspension source area impacts at Rocky Flats surveillance air samplers S-7 and S-8, July 25-August 25, 1983 and September 8-October 4, 1983

    SciTech Connect (OSTI)

    Hammer, R.J.

    1984-01-01

    An on-going study at the Rocky Flats Plant is being used to evaluate resuspension source area contributions to Pu-239 concentrations at 2 of the samplers in the Plants air sampling network. Early results from the study indicate that Pu-239 concentration levels are being affected primarily by resuspension from a zone 150 meters east and west of the study samplers. Initial results have also shown that net transport of Pu-239 during the sampling period has been from the east toward the west, onto the plant proper. These early findings show that sources immediately east of the 2 samplers are responsible for most of the Pu-239 exposure at the samplers. 2 references, 1 figure, 4 tables.

  10. Molecular Cell, Volume 54 Supplemental Information

    E-Print Network [OSTI]

    Rohs, Remo

    in the nucleotides upstream (up, sequence underlined) or downstream (dw), or both mutations upstream and downstream mutated in both the two nucleotides upstream and downstream of the Pu.1 sites. B) #12; Competitive

  11. PostScript

    E-Print Network [OSTI]

    2015-11-19

    ... (DNS) but at signi cantly less cost so that one can simulate more complicated ..... where p = (pu; pv; pw) and similarly for q and r: The decomposition (2.16) on ...

  12. Maximum Fuel Utilization in Advanced Fast Reactors without Actinides Separation

    E-Print Network [OSTI]

    Heidet, Florent

    2010-01-01

    1996. 12 p. Toshinsky, G.I. , LMFBR Operation in the Nuclearand characterization of LMFBR carbide and nitride fuels andcores with oxide fuel, “LMFBR recycle Pu/U”, are used.

  13. Non-destructive Assay Measurements Using the RPI Lead Slowing...

    Office of Scientific and Technical Information (OSTI)

    consid- ered as a possible option for non-destructive assay of fissile material of used nuclear fuel. The primary objective is to quantify the 239Pu and 235U fissile content via...

  14. Monte Carlo Hauser-Feshbach Calculations of Prompt Fission Neutrons...

    Office of Scientific and Technical Information (OSTI)

    Technical Report: Monte Carlo Hauser-Feshbach Calculations of Prompt Fission Neutrons and Gamma Rays: Application to Thermal Neutron-Induced Fission Reactions on U-235 and Pu-239...

  15. Effect of Spin-Orbit Coupling on the Actinide Dioxides AnO2 ...

    Office of Scientific and Technical Information (OSTI)

    Coupling on the Actinide Dioxides AnO2 (AnTh, Pa, U, Np, Pu, and Am): A Screened Hybrid Density Functional Study Citation Details In-Document Search Title: Effect of...

  16. GEOCHEMISTRY AND ISOTOPE HYDROLOGY OF GROUNDWATERS IN THE STRIPA GRANITE RESULTS AND PRELIMINARY INTERPRETATION

    E-Print Network [OSTI]

    Fritz, P.

    2011-01-01

    in the aquifer rocks, and helium production from uranium andwhere U:Th tal rocks. Helium production rates are Pu uraniumhelium and sometimes argon can alter the noble gas ratios, notably in geothermal areas. If the production

  17. NNSA releases Stockpile Stewardship Program quarterly experiments...

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    in particular the first Pu experiment on NIF, the return to operations of the TA-55 gas gun, a successful series of plutonium experiments on Joint Actinide Shock Physics...

  18. IntOPIntOP 20152015IntOP 2015 The 3rd Workshop of the European Multi-scale

    E-Print Network [OSTI]

    Adler, Joan

    Cost-effective CO2 capture processes Y Micro- and nanofluid systems for in vitro diagnostics (IVD) Y Enhanced LED performance Y Enhanced photovoltaic device efficiency Y Enhanced polyurethane foams (PU) Y

  19. Radiochim. Acta 93, 265272 (2005) by Oldenbourg Wissenschaftsverlag, Mnchen

    E-Print Network [OSTI]

    Utsunomiya, Satoshi

    2005-01-01

    fuel cycle in the US is operated in a once-through mode with SNF in- tended for direct disposal irradiation time, the remainder consists of approximately 1% plutonium (Pu), 2%­3% fission products, and other

  20. Investigations on the sediment chronology and trace metal accumulation in Sabine-Neches estuary, Beaumont, Texas 

    E-Print Network [OSTI]

    Ravichandran, Mahalingam

    1994-01-01

    geochronology of sediments and reconstruction of the history of trace metal inputs into this shallow estuarine environment was possible because the 239,240pu profiles closely tracked the bomb fallout history into the environment. The sedimentation rate...

  1. Feasibility of breeding in hard spectrum boiling water reactors with oxide and nitride fuels

    E-Print Network [OSTI]

    Feng, Bo, Ph. D. Massachusetts Institute of Technology

    2011-01-01

    This study assesses the neutronic, thermal-hydraulic, and fuel performance aspects of using nitride fuel in place of oxides in Pu-based high conversion light water reactor designs. Using the higher density nitride fuel ...

  2. Quantifying the Safety Effects of Access Management Using VISSIM and SSAM: A Case Study

    E-Print Network [OSTI]

    Argade, Prathmesh

    2014-12-31

    to Ousdahl Road ......................................... 43 Figure 27: Desired Vehicle Speed Distribution ................................................................ 45 Figure 28: Links and Connectors... High Model ...................................................................................... 54 Figure 36: SSAM Work Flow Diagram (Source: Pu and Joshi, 2008) ............................. 55 Figure 37: Exporting SSAM Vehicle Trajectory Data...

  3. June 2015 Most Viewed Documents for Fission And Nuclear Technologies...

    Office of Scientific and Technical Information (OSTI)

    June 2015 Most Viewed Documents for Fission And Nuclear Technologies Estimation of gas leak rates through very small orifices and channels. From sealed PuOsub 2 containers under...

  4. Transparency Reforms: Theory and Practice

    E-Print Network [OSTI]

    Fox, Jonathan A; Haight, Libby

    2011-01-01

    y ´blica (CIDE). Pol?´tica Pu Fung, A. , Graham, M. , &information sites, see Pol?´ tica Digital (2009). 13. Theon July 10, 2010. Pol?´ tica Digital. (2009). Ranking de

  5. IMPACT OF FISSION PRODUCTS IMPURITY ON THE PLUTONIUM CONTENT IN PWR MOX FUELS

    SciTech Connect (OSTI)

    Gilles Youinou; Andrea Alfonsi

    2012-03-01

    This report presents the results of a neutronics analysis done in response to the charter IFCA-SAT-2 entitled 'Fuel impurity physics calculations'. This charter specifies that the separation of the fission products (FP) during the reprocessing of UOX spent nuclear fuel assemblies (UOX SNF) is not perfect and that, consequently, a certain amount of FP goes into the Pu stream used to fabricate PWR MOX fuel assemblies. Only non-gaseous FP have been considered (see the list of 176 isotopes considered in the calculations in Appendix 1). This mixture of Pu and FP is called PuFP. Note that, in this preliminary analysis, the FP losses are considered element-independent, i.e., for example, 1% of FP losses mean that 1% of all non-gaseous FP leak into the Pu stream.

  6. Design and fabrication of physiologic tissue scaffolds using projection-micro-stereolithography

    E-Print Network [OSTI]

    Brickman Raredon, Micha Sam

    2014-01-01

    Recent advances in material processing are presenting groundbreaking opportunities for biomedical engineers. Projection-micro-stereolithography, or PuSL, is an additive manufacturing technique in which complex parts are ...

  7. CX-011355: Categorical Exclusion Determination

    Broader source: Energy.gov [DOE]

    Receipt, Unloading, and Movement of Radioactive Samples in Support of the 3013 Pu Surveillance Program CX(s) Applied: B3.6 Date: 09/09/2013 Location(s): South Carolina Offices(s): Savannah River Operations Office

  8. Special isotope separation at the Idaho National Engineering Laboratory

    SciTech Connect (OSTI)

    Hendrickson, P.D.

    1989-02-03

    The SIS facilities will include a Plutonium Processing Facility (PPF), a Laser Support Facility (LSF), and all associated equipment required for isotope separation. The SIS Plant will process fuel-grade plutonium into weapons-grade plutonium using Atomic Vapor Laser Isotope Separation (AVLIS) and supporting chemical processes. The AVLIS process uses precisely tuned visible laser light to selectively ionize or excite specific plutonium isotopes in a vapor stream. The ionized plutonium isotopes (Pu 240, Pu 238 and Pu 241) are then separated from the plutonium isotope of interest (Pu 239). Chemical processes are required to (1) prepare the AVLIS plutonium feed for processing, remove americium-241, and cast plutonium metal into forms that meet AVLIS processing requirements; (2) recover and, if required, purify the AVLIS plutonium product; and (3) recover and process the AVLIS separated by-products. This presentation describes the production facility and some of the plutonium processes.

  9. Plutonium dissolution process

    DOE Patents [OSTI]

    Vest, M.A.; Fink, S.D.; Karraker, D.G.; Moore, E.N.; Holcomb, H.P.

    1994-01-01

    A two-step process for dissolving Pu metal is disclosed in which two steps can be carried out sequentially or simultaneously. Pu metal is exposed to a first mixture of 1.0-1.67 M sulfamic acid and 0.0025-0.1 M fluoride, the mixture having been heated to 45-70 C. The mixture will dissolve a first portion of the Pu metal but leave a portion of the Pu in an oxide residue. Then, a mineral acid and additional fluoride are added to dissolve the residue. Alternatively, nitric acid between 0.05 and 0.067 M is added to the first mixture to dissolve the residue as it is produced. Hydrogen released during the dissolution is diluted with nitrogen.

  10. Dissolution Kinetics of Pyrochlore Ceramics for the Disposition of Plutonium.

    SciTech Connect (OSTI)

    Icenhower, Jonathan P.; Strachan, Denis M.; McGrail, B. Peter; Scheele, Randall D.; Rodriguez, Elsa A.; Steele, Jackie L.; Legore, Virginia L.

    2006-01-30

    This is an article in which the dissolution kinetics of titanate ceramics are reported and discussed. These ceramics are made with non-radioactive elements as analogues to those made with Pu.

  11. PLUTONIUM SOLUBILITY IN SIMULATED SAVANNAH RIVER SITE WASTE SOLUTIONS

    SciTech Connect (OSTI)

    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 measured or values predicted by the SRNL model and values predicted by the OLI AG model was very poor. The much higher predicted concentrations by the OLI AQ model appears to be the result of the model predicting the predominate Pu oxidation state is Pu(V) which is reported as unstable below sodium hydroxide (NaOH) concentrations of 6 M. There was very good agreement between the predicted Pu concentrations using the SRNL model and the model developed by Delegard and Gallagher with the exception of solutions that had very high OH{sup -} (15 M) concentrations. The lower Pu solubilities in these solutions were attributed to the presence of NO{sub 3}{sup -} and NO{sub 2}{sup -} which limit the oxidation of Pu(IV) to Pu(V).

  12. Khesbn No. 37, May 1964 - Entire Journal

    E-Print Network [OSTI]

    1964-01-01

    px nan 18H8P P3NW1 man px nan e>teya> inox man ppiga îan Wflg nynn 8'te ypaxaw inox ttK11í? ga *n fig gPiyi aiyaayiga pu

  13. Measurement of plutonium and americium volatilities under thermal process conditions. Final report

    SciTech Connect (OSTI)

    Krikorian, O.H.; Condit, R.H.; Fontes, A.S. Jr.; Fleming, D.L.; Magana, J.W.; Morris, W.F.; Adamson, M.G.

    1993-04-28

    We have used the transpiration method to measure volatilities of Pu and Am from PuO{sub 2}(s) and PuO{sub 2}/2% AmO{sub 2}(s) in the presence of steam and oxygen at temperatures of 1230--1430 K. We find the volatile species to be PuO{sub 2}(OH){sub 2}(g) and AmO{sub 2}(OH){sub 2}(g) at vapor pressures on the order of 10{sup {minus}10} atm and 10 {sup {minus}12} atm respectively under measurement conditions. For the Pu volatilization reaction, PuO{sub 2}(s) + 1/2 0{sub 2}(9) + H{sub 2}0(g) = PuO{sub 2}(OH){sub 2}(g), we obtain a free energy of reaction of {Delta}G{sup O}{sub T} = 231.3--0.0109 T in kj/mol, and for the Am volatilization reaction, AmO{sub 2}(s.s. in PuO{sub 2}) + 1/2 0{sub 2}(9) + H{sub 2}0(g) = AmO{sub 2}(OH){sub 2}(g), we obtain AG{sup O}{sub T} = 223.9--0.0109 T in kj/mol. We apply these results to the Rocky Flats Plant Fluidized Bed Incinerator to assess the amount of volatile Pu and Am produced in the secondary combustor chamber. Taking operating conditions of 550C combustor temperature, 40 kmols/h of total gas flow at 1 atm pressure, 0.1 atm 0{sub 2}(9), 0.05 atm H{sub 2}0(g), PuO{sub 2} (s) containing 200 ppm AmO{sub 2} in the bed, and 6000 h of operating time per year, gives volatilization rates of 7 {times} 10 {sup {minus}6}g Pu and 4 {times} 10 {sup {minus}9}g Am/y.

  14. EVALUATION OF FLOWSHEET CHANGES FOR THE HIGHLY ENRICHED URANIUM BLENDDOWN PROGRAM

    SciTech Connect (OSTI)

    Crowder, M.; Rudisill, T.; Laurinat, J.; Mickalonis, J.

    2007-10-22

    H Canyon is considering a flowsheet change for Plutonium (Pu) Contaminated Scrap (PuCS) material. The proposed change is to route dissolved PuCS material directly to a uranium (U) storage tank. As a result, the PuCS solution will bypass Head End and First U Cycle, and will be purified by solvent extraction in Second U Cycle. The PuCS solution contains appreciable amounts of boron (B) and fluoride (F{sup -}), which are currently at trace levels in the U storage tank. Though unlikely, if the B concentration in the U storage tank were to reach 1.8 g B/g U, the entire contents of the U storage tank would likely require a second pass through Second U Cycle to provide sufficient decontamination to meet the Tennessee Valley Authority (TVA) Blend Grade Highly Enriched Uranium (HEU) specification for B, which is 30 {micro}g/g U. In addition, Second U Cycle is expected to provide sufficient decontamination of F{sup -} and Pu regardless of the amount of PuCS solution sent to the storage tank. Though aluminum (Al) is not present in the PuCS solution, B can be credited as a complexant of F{sup -}. Both stability constants from the literature and Savannah River National Laboratory (SRNL) corrosion studies were documented to demonstrate that B complexation of F{sup -} in nitric acid solutions is sufficient to prevent excessive corrosion. Though B and Al complex F{sup -} to a similar degree, neither completely eliminates the presence of free F{sup -} in solution. Therefore, a limited amount of corrosion is expected even with complexed F{sup -} solutions. Tanks maintained at ambient temperature are not expected to experience significant corrosion. However, the Low Activity Waste (LAW) evaporators may be subjected to a corrosion rate of about 25 mils per year (mpy) as they reach their highest F{sup -} concentrations. The feed adjustment evaporator would only be subjected to the corrosion rate of about 25 mpy in the latter stages of the PuCS campaign. An issue that must be addressed as part of the proposed PuCS flowsheet change is that B has limited solubility in concentrated nitric acid solutions. As the proposed PuCS campaign progresses, the B concentration will increase in the U storage tank, in Second U Cycle feed, and in the 1DW stream sent to the LAW evaporators. Limitations on the B concentration in the LAW evaporators will be needed to prevent formation of boron-containing solids.

  15. Selected papers for global `95 concerning plutonium

    SciTech Connect (OSTI)

    Sutcliffe, W.G.

    1996-06-14

    This report contains selected papers from the Global `95 Conference ``Evaluation of Emerging Nuclear Fuel Cycle Systems,`` held in Versailles, Sept. 11-14, 1995. The 11 papers in Part I are from ``Benefits and Risks of Reprocessing`` sessions. The 7 papers in Part II are some of the more interesting poster papers that relate to the use of Pu for power generation. Finally, the 3 papers are on the topic of management and disposition of Pu from retired nuclear weapons.

  16. Annual progress Report on research related to our research project “Stabilization of Plutonium in Subsurface Environments via Microbial Reduction and Biofilm Formation” funded by the Environmental Remediation Sciences Division (ERSD)

    SciTech Connect (OSTI)

    New, Mary

    2006-06-01

    The overarching goal of this research project is to investigate and optimize the mechanisms for in situ immobilization of Pu species by naturally-occurring bacteria. Specific research objectives are: (a) investigate the mechanism of bacterial accumulation and immobilization of plutonium species by biofilm formation under aerobic conditions and (b) to demonstrate the direct and indirect stabilization of Pu via dissimilatory reduction by Geobacter metallireducens.

  17. Nuclear Data Sheets for A=228

    SciTech Connect (OSTI)

    Abusaleem, Khalifeh

    2014-02-01

    The evaluated spectroscopic data are presented for known nuclides of mass 228 (Ac, At, Fr, Np, Pa, Pu, Ra, Rn, Th, and U). Excited states in {sup 228}At, {sup 228}Rn, {sup 228}Fr, {sup 228}Np, and {sup 228}Pu have not been identified as yet. Significant amounts of new data have been added since the last evaluation of A=228 nuclides. This work supersedes earlier full evaluations of A=228 published by 1997Ar08.

  18. Affinity of An(VI) for N4-Tetradentate Donor Ligands: Complexation of the Actinyl(VI) Ions with N4-Tetradentate Ligands

    SciTech Connect (OSTI)

    Ogden, Mark; Sinkov, Sergey I.; Lumetta, Gregg J.; Nash, Kenneth L.

    2012-05-01

    In this report the affinity of four N4-tetradentate ligands that incorporate the 2- methylpyridyl functionality with hexavalent actinides (AnO2+2 ) has been investigated in methanol solution. The ligands studied include N,N*-bis(2-methylpyridyl)diaminoethane (BPMDAE), N,N-bis(2-methylpyridyl)-1,3-diaminopropane (BPMDAP), N,N*-bis(2-pyridylmethyl) piperazine (BPMPIP), and trans-N,N-bis(2-pyridylmethyl)-1,2-diaminocyclohexane (BPMDAC). Conditional stability constants describing the strength of the interaction were determined by UV-visible spectrophotometry. The log10K101 values for both U(VI) and Pu(VI) are comparable and show the same trend of stability with ligand structure. Dinuclear complexes are also indicated as being important. The log10K201 values for Pu(VI) complexation with the N4-ligands are identical for the four ligands (within experimental error), indicating that the structure of the ligand backbone has little effect on the stability of the (PuO2)2L2+ complex. The exception to this trend is the behavior of N,N*- bis(2-pyridylmethyl)piperazine (BPMPIP) with Pu(VI). This ligand displays a tendency to reduce Pu(VI) within the experimental time frame of 45 minutes. BPMPIP is the only ligand tested that contains tertiary amines in the ligand backbone. The decomposition of BPMPIP by Pu(VI) suggests a susceptibility of tertiary amines to oxidative degradation.

  19. Plutonium Isotopes in the Terrestrial Environment at the Savannah River Site, USA: A Long-Term Study

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Armstrong, Christopher R.; Brant, Heather A.; Nuessle, Patterson R.; Hall, Gregory; Halverson, Justin E.; Cadieux, James R.

    2015-02-03

    This work presents the findings of a long term plutonium study at Savannah River Site (SRS) conducted between 2003 and 2013. Terrestrial environmental samples were obtained at Savannah River National Laboratory (SRNL) in A-area. Plutonium content and isotopic abundances were measured over this time period by alpha spectrometry and three stage thermal ionization mass spectrometry (3STIMS). Here we detail the complete sample collection, radiochemical separation, and measurement procedure specifically targeted to trace plutonium in bulk environmental samples. Total plutonium activities were determined to be not significantly above atmospheric global fallout. However, the 238Pu/239+240Pu activity ratios attributed to SRS are above atmospheric global fallout ranges. The 240Pu/239Pu atom ratios are reasonably consistent from year to year and are lower than fallout, while the 242Pu/239Pu atom ratios are higher than fallout values. Overall, the plutonium signatures obtained in this study reflect a mixture of weapons-grade, higher burn-up, and fallout material. This study provides a blue print for long term low level monitoring of plutonium in the environment.

  20. Preparation of actinide specimens for the US/UK joint experiment in the Dounreay Prototype Fast Reactor

    SciTech Connect (OSTI)

    Quinby, T C; Adair, H L; Kobisk, E H

    1982-05-01

    A joint research program involving the United States and the United Kingdom was initiated about four years ago for the purpose of studying the fuel behavior of higher actinides using in-core irradiation in the fast reactor at Dounreay, Scotland. Simultaneously, determination of integral cross sections of a wide variety of higher actinide isotopes (physics specimens) was proposed. Coincidental neutron flux and energy spectral measurements were to be made using vanadium encapsulated dosimetry materials in the immediate region of the fuel pellets and physics samples. The higher actinide samples chosen for the fuel study were /sup 241/Am and /sup 244/Cm in the forms of Am/sub 2/O/sub 3/, Cm/sub 2/O/sub 3/, and Am/sub 6/Cm(RE)/sub 7/O/sub 21/, where (RE) represents a mixture of lanthanides. Milligram quantities of actinide oxides of /sup 248/Cm, /sup 246/Cm, /sup 244/Cm, /sup 243/Cm, /sup 243/Am, /sup 241/Am, /sup 244/Pu, /sup 242/Pu, /sup 241/Pu, /sup 240/Pu, /sup 239/Pu, /sup 238/Pu, /sup 237/Np, /sup 238/U, /sup 236/U, /sup 235/U, /sup 234/U, /sup 233/U, /sup 232/Th, /sup 230/Th, and /sup 231/Pa were encapsulated to obtain nuclear cross section and reaction rate data for these materials.

  1. Thermal Degradation Studies of Polyurethane/POSS Nanohybrid Elastomers

    SciTech Connect (OSTI)

    Lewicki, J P; Pielichowski, K; TremblotDeLaCroix, P; Janowski, B; Todd, D; Liggat, J J

    2010-03-05

    Reported here is the synthesis of a series of Polyurethane/POSS nanohybrid elastomers, the characterization of their thermal stability and degradation behavior at elevated temperatures using a combination of Thermal Gravimetric Analysis (TGA) and Thermal Volatilization Analysis (TVA). A series of PU elastomers systems have been formulated incorporating varying levels of 1,2-propanediol-heptaisobutyl-POSS (PHIPOSS) as a chain extender unit, replacing butane diol. The bulk thermal stability of the nanohybrid systems has been characterized using TGA. Results indicate that covalent incorporation of POSS into the PU elastomer network increase the non-oxidative thermal stability of the systems. TVA analysis of the thermal degradation of the POSS/PU hybrid elastomers have demonstrated that the hybrid systems are indeed more thermally stable when compared to the unmodified PU matrix; evolving significantly reduced levels of volatile degradation products and exhibiting a {approx}30 C increase in onset degradation temperature. Furthermore, characterization of the distribution of degradation products from both unmodified and hybrid systems indicate that the inclusion of POSS in the PU network is directly influencing the degradation pathways of both the soft and hard block components of the elastomers: The POSS/PU hybrid systems show reduced levels of CO, CO2, water and increased levels of THF as products of thermal degradation.

  2. Disposition of excess weapons plutonium from dismantled weapons

    SciTech Connect (OSTI)

    Jardine, L.J.

    1997-01-01

    With the end of the Cold War and the implementation of various nuclear arms reduction agreements, US and Russia have been actively dismantling tens of thousands of nuclear weapons. As a result,large quantities of fissile materials, including more than 100 (tonnes?) of weapons-grade Pu, have become excess to both countries` military needs. To meet nonproliferation goals and to ensure the irreversibility of nuclear arms reductions, this excess weapons Pu must be placed in secure storage and then, in timely manner, either used in nuclear reactors as fuel or discarded in geologic repositories as solid waste. This disposition in US and Russia must be accomplished in a safe, secure manner and as quickly as practical. Storage of this Pu is a prerequisite to any disposition process, but the length of storage time is unknown. Whether by use as fuel or discard as solid waste, disposition of that amount of Pu will require decades--and perhaps longer, if disposition operations encounter delays. Neither US nor Russia believes that long-term secure storage is a substitute for timely disposition of excess Pu, but long-term, safe, secure storage is a critical element of all excess Pu disposition activities.

  3. Plutonium Isotopes in the Terrestrial Environment at the Savannah River Site, USA. A Long-Term Study

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Armstrong, Christopher R.; Nuessle, Patterson R.; Brant, Heather A.; Hall, Gregory; Halverson, Justin E.; Cadieux, James R.

    2015-01-16

    This work presents the findings of a long term plutonium study at Savannah River Site (SRS) conducted between 2003 and 2013. Terrestrial environmental samples were obtained at Savannah River National Laboratory (SRNL) in A-area. Plutonium content and isotopic abundances were measured over this time period by alpha spectrometry and three stage thermal ionization mass spectrometry (3STIMS). Here we detail the complete sample collection, radiochemical separation, and measurement procedure specifically targeted to trace plutonium in bulk environmental samples. Total plutonium activities were determined to be not significantly above atmospheric global fallout. However, the 238Pu/239+240Pu activity ratios attributed to SRS are abovemore »atmospheric global fallout ranges. The 240Pu/239Pu atom ratios are reasonably consistent from year to year and are lower than fallout, while the 242Pu/239Pu atom ratios are higher than fallout values. Overall, the plutonium signatures obtained in this study reflect a mixture of weapons-grade, higher burn-up, and fallout material. This study provides a blue print for long term low level monitoring of plutonium in the environment.« less

  4. INTERPRETATION OF AT-LINE SPECTRA FROM AFS-2 BATCH #3 FERROUS SULFAMATE TREATMENT

    SciTech Connect (OSTI)

    Kyser, E.; O'Rourke, P.

    2013-12-10

    Spectra from the “at-line” spectrometer were obtained during the ferrous sulfamate (FS) valence adjustment step of AFS-2 Batch #3 on 9/18/2013. These spectra were analyzed by mathematical principal component regression (PCR) techniques to evaluate the effectiveness of this treatment. Despite the complications from Pu(IV), we conclude that all Pu(VI) was consumed during the FS treatment, and that by the end of the treatment, about 85% was as Pu(IV) and about 15% was as Pu(III). Due to the concerns about the “odd” shape of the Pu(IV) peak and the possibility of this behavior being observed in the future, a follow-up sample was sent to SRNL to investigate this further. Analysis of this sample confirmed the previous results and concluded that it “odd” shape was due to an intermediate acid concentration. Since the spectral evidence shows complete reduction of Pu(VI) we conclude that it is appropriate to proceed with processing of this the batch of feed solution for HB-Line including the complexation of the fluoride with aluminum nitrate.

  5. Implications of Plutonium isotopic separation on closed fuel cycles and repository design

    SciTech Connect (OSTI)

    Forsberg, C.

    2013-07-01

    Advances in laser enrichment may enable relatively low-cost plutonium isotopic separation. This would have large impacts on LWR closed fuel cycles and waste management. If Pu-240 is removed before recycling plutonium as mixed oxide (MOX) fuel, it would dramatically reduce the buildup of higher plutonium isotopes, Americium, and Curium. Pu-240 is a fertile material and thus can be replaced by U-238. Eliminating the higher plutonium isotopes in MOX fuel increases the Doppler feedback, simplifies reactor control, and allows infinite recycle of MOX plutonium in LWRs. Eliminating fertile Pu-240 and Pu-242 reduces the plutonium content in MOX fuel and simplifies fabrication. Reducing production of Pu-241 reduces production of Am-241 - the primary heat generator in spent nuclear fuels after several decades. Reducing heat generating Am-241 would reduce repository cost and waste toxicity. Avoiding Am- 241 avoids its decay product Np-237, a nuclide that partly controls long-term oxidizing repository performance. Most of these benefits also apply to LWR plutonium recycled into fast reactors. There are benefits for plutonium isotopic separation in fast reactor fuel cycles (particularly removal of Pu-242) but the benefits are less. (author)

  6. Melting temperatures of the ZrO{sub 2}-MOX system

    SciTech Connect (OSTI)

    Uchida, T.; Hirooka, S.; Kato, M.; Morimoto, K.; Sugata, H.; Shibata, K.; Sato, D.

    2013-07-01

    Severe accidents occurred at the Fukushima Daiichi Nuclear Power Plant Units 1-3 on March 11, 2011. MOX fuels were loaded in the Unit 3. For the thermal analysis of the severe accident, melting temperature and phase state of MOX corium were investigated. The simulated coriums were prepared from 4%Pu-containing MOX, 8%Pu-containing MOX and ZrO{sub 2}. Then X-ray diffraction, density and melting temperature measurements were carried out as a function of zirconium and plutonium contents. The cubic phase was observed in the 25%Zr-containing corium and the tetragonal phase was observed in the 50% and 75%Zr-containing coria. The lattice parameter and density monotonically changed with Pu content. Melting temperature increased with increasing Pu content; melting temperature were estimated to be 2932 K for 4%Pu MOX corium and 3012 K for 8%Pu MOX corium in the 25%ZrO{sub 2}-MOX system. The lowest melting temperature was observed for 50%Zr-containing corium. (authors)

  7. SU-E-T-315: The Change of Optically Stimulated Luminescent Dosimeters (OSLDs) Sensitivity by Accumulated Dose and High Dose

    SciTech Connect (OSTI)

    Han, S; Jung, H; Kim, M; Ji, Y; Kim, K [University of Science and Technology, Daejeon (Korea, Republic of); Korea Institute of Radiological and Medical Sciences, Seoul (Korea, Republic of); Choi, S; Park, S; Yoo, H [Korea Institute of Radiological and Medical Sciences, Seoul (Korea, Republic of); Yi, C [Korea Research Institute of Standards and Science, Daejeon (Korea, Republic of)

    2014-06-01

    Purpose: The objective of this study is to evaluate radiation sensitivity of optical stimulated luminance dosimeters (OSLDs) by accumulated dose and high dose. Methods: This study was carried out in Co-60 unit (Theratron 780, AECL, and Canada) and used InLight MicroStar reader (Landauer, Inc., Glenwood, IL) for reading. We annealed for 30 min using optical annealing system which contained fluorescent lamps (Osram lumilux, 24 W, 280 ?780 nm). To evaluate change of OSLDs sensitivity by repeated irradiation, the dosimeters were repeatedly irradiated with 1 Gy. And whenever a repeated irradiation, we evaluated OSLDs sensitivity. To evaluate OSLDs sensitivity after accumulated dose with 5 Gy, We irradiated dose accumulatively (from 1 Gy to 5 Gy) without annealing. And OSLDs was also irradiated with 15, 20, 30 Gy to certify change of OSLDs sensitivity after high dose irradiation. After annealing them, they were irradiated with 1Gy, repeatedly. Results: The OSLDs sensitivity increased up to 3% during irradiating seven times and decreased continuously above 8 times. That dropped by about 0.35 Gy per an irradiation. Finally, after 30 times irradiation, OSLDs sensitivity decreased by about 7%. For accumulated dose from 1 Gy to 5 Gy, OSLDs sensitivity about 1 Gy increased until 4.4% after second times accumulated dose compared with before that. OSLDs sensitivity about 1 Gy decreased by 1.6% in five times irradiation. When OSLDs were irradiated ten times with 1Gy after irradiating high dose (10, 15, 20 Gy), OSLDs sensitivity decreased until 6%, 9%, 12% compared with it before high dose irradiation, respectively. Conclusion: This study certified OSLDs sensitivity by accumulated dose and high dose. When irradiated with 1Gy, repeatedly, OSLDs sensitivity decreased linearly and the reduction rate of OSLDs sensitivity after high dose irradiation had dependence on irradiated dose.

  8. Studies of Plutonium Aerosol Resuspension at the Time of the Maralinga Cleanup

    SciTech Connect (OSTI)

    Shinn, J

    2003-08-01

    At the former nuclear test site at Maralinga, South Australia, soil cleanup began in October 1996 with the objective to remove the potential for residual plutonium (Pu) exposures to the public. In this case the cleanup was to restore access to the closed test site. The proposed long-term land use was primarily to be a hunting area for Pitjantjatjara (Aboriginal) people, but also presumably to be available to the public who might have an interest in the history of the site. The long-term management objective for the site was to allow casual use, but to prohibit habitation. The goal of this study is to provide an evaluation of the Maralinga soil cleanup in terms of potential long-term public inhalation exposures to particulate Pu, and in terms of a contribution to planning and conducting any such soil Pu-cleanup. Such cleanups might be carried out for example, on the Nevada Test Site in the United States. For Pu that has been deposited on the soil by atmospheric sources of finely divided particles, the dominant exposure pathway to humans is by inhalation. Other exposure pathways are less important because the Pu particles become oxidized into a nearly insoluble form, do not easily enter into the food chain, nor are they significantly transferred through the intestine to the bloodstream should Pu become ingested. The purpose of this report is to provide results of the Pu resuspension measurements made before, during, and after the Pu cleanup at Maralinga, to compare these against similar measurements made elsewhere, and to interpret the results as they relate to potential long-term public exposures. (Exposures to Pu in dust plumes produced by mechanical disturbance during cleanup are considered short-term, unlikely to be significant for purposes of this report, and are not included). A considerable amount of research had been conducted at Maralinga by the Australian Radiation Laboratory, now the Australian Radiation Protection and Nuclear Safety Agency (ARPANSA), prior to the cleanup (Johnston et al, 1992, Williams 1993, Johnston et al 1993, Burns et al 1994, Burns et al 1995). ARPANSA staff made major contributions to delineate the areas with Pu in the soil, to determine the degree of secondary soil contamination by fission products from nuclear testing, to measure Pu resuspension by wind erosion of the undisturbed soil, and to prepare assessments of the human health risk from residual soil Pu. In addition, ARPANSA supported the Maralinga cleanup to assure compliance with criteria set by an independent technical advisory committee. During the cleanup ARPANSA monitored the residual Pu in the soil and certified that the cleanup was complete according to the criteria. It was not the reduction in potential inhalation exposure that usually was the main driver of the cleanup, but the requirement to also remove individual hot particles and fragments. It is the residual microscopic particles of Pu in the soil, however, that have the potential for long-term human exposure. The resuspension of respirable-size Pu particles has been studied with specialized equipment at the Nevada Test Site (Gilbert et al 1988a, Gilbert et al 1988b, Shinn et al 1989, and Shinn 1992), and at Bikini and Enewetak in the Marshall Islands (Shinn et al 1997). These efforts were in large part contributed by the Health and Ecological Assessment Division, University of California, Lawrence Livermore National Laboratory (LLNL). The study reported here is a collaboration between ARPANSA and LLNL, and was jointly supported by the United States Department of Energy, and the Commonwealth of Australia Department of Primary Industry and Energy.

  9. GRAVITATIONAL WAVES FROM MASSIVE MAGNETARS FORMED IN BINARY NEUTRON STAR MERGERS

    SciTech Connect (OSTI)

    Dall'Osso, Simone [Theoretical Astrophysics, University of Tübingen, auf der Morgenstelle 10 D-72076 (Germany); Giacomazzo, Bruno [Physics Department, University of Trento, via Sommarive 14, I-38123 Trento (Italy); Perna, Rosalba [Department of Physics and Astronomy, Stony Brook University, Stony Brook, NY 11794 (United States); Stella, Luigi, E-mail: simone.dallosso@uni-tuebingen.de [INAF-Osservatorio Astronomico di Roma, via di Frascati 33, I-00040 Monteporzio Catone, Roma (Italy)

    2015-01-01

    Binary neutron star (NS) mergers are among the most promising sources of gravitational waves (GWs), as well as candidate progenitors for short gamma-ray bursts (SGRBs). Depending on the total initial mass of the system and the NS equation of state (EOS), the post-merger phase can be characterized by a prompt collapse to a black hole or by the formation of a supramassive NS, or even a stable NS. In the latter cases of post-merger NS (PMNS) formation, magnetic field amplification during the merger will produce a magnetar and induce a mass quadrupole moment in the newly formed NS. If the timescale for orthogonalization of the magnetic symmetry axis with the spin axis is smaller than the spindown time, the NS will radiate its spin down energy primarily via GWs. Here we study this scenario for the various outcomes of NS formation: we generalize the set of equilibrium states for a twisted torus magnetic configuration to include solutions that, for the same external dipolar field, carry a larger magnetic energy reservoir; we hence compute the magnetic ellipticity for such configurations, and the corresponding strength of the expected GW signal as a function of the relative magnitude of the dipolar and toroidal field components. The relative number of GW detections from PMNSs and from binary NSs is a very strong function of the NS EOS, being higher (?1%) for the stiffest EOSs and negligibly small for the softest ones. For intermediate-stiffness EOSs, such as the n = 4/7 polytrope recently used by Giacomazzo and Perna or the GM1 used by Lasky et al., the relative fraction is ?0.3%; correspondingly, we estimate a GW detection rate from stable PMNSs of ?0.1-1 yr{sup –1} with advanced detectors, and of ?100-1000 yr{sup –1} with detectors of third generation such as the Einstein Telescope. Measurement of such GW signals would provide constraints on the NS EOS and, in connection with an SGRB, on the nature of the binary progenitors giving rise to these events.

  10. FORM AND AGING OF PLUTONIUM IN SAVANNAH RIVER SITE WASTE TANK 18

    SciTech Connect (OSTI)

    Hobbs, D.

    2012-02-24

    This report provides a summary of the effects of aging on and the expected forms of plutonium in Tank 18 waste residues. The findings are based on available information on the operational history of Tank 18, reported analytical results for samples taken from Tank 18, and the available scientific literature for plutonium under alkaline conditions. These findings should apply in general to residues in other waste tanks. However, the operational history of other waste tanks should be evaluated for specific conditions and unique operations (e.g., acid cleaning with oxalic acid) that could alter the form of plutonium in heel residues. Based on the operational history of other tanks, characterization of samples from the heel residues in those tanks would be appropriate to confirm the form of plutonium. During the operational period and continuing with the residual heel removal periods, Pu(IV) is the dominant oxidation state of the plutonium. Small fractions of Pu(V) and Pu(VI) could be present as the result of the presence of water and the result of reactions with oxygen in air and products from the radiolysis of water. However, the presence of Pu(V) would be transitory as it is not stable at the dilute alkaline conditions that currently exists in Tank 18. Most of the plutonium that enters Savannah River Site (SRS) high-level waste (HLW) tanks is freshly precipitated as amorphous plutonium hydroxide, Pu(OH){sub 4(am)} or hydrous plutonium oxide, PuO{sub 2(am,hyd)} and coprecipitated within a mixture of hydrous metal oxide phases containing metals such as iron, aluminum, manganese and uranium. The coprecipitated plutonium would include Pu{sup 4+} that has been substituted for other metal ions in crystal lattice sites, Pu{sup 4+} occluded within hydrous metal oxide particles and Pu{sup 4+} adsorbed onto the surface of hydrous metal oxide particles. The adsorbed plutonium could include both inner sphere coordination and outer sphere coordination of the plutonium. PuO{sub 2(am,hyd)} is also likely to be present in deposits and scales that have formed on the steel surfaces of the tank. Over the operational period and after closure of Tank 18, Ostwald ripening has and will continue to transform PuO{sub 2(am,hyd)} to a more crystalline form of plutonium dioxide, PuO{sub 2(c)}. After bulk waste removal and heel retrieval operations, the free hydroxide concentration decreased and the carbonate concentration in the free liquid and solids increased. Consequently, a portion of the PuO{sub 2(am,hyd)} has likely been converted to a hydroxy-carbonate complex such as Pu(OH){sub 2}(CO{sub 3}){sub (s)}. or PuO(CO{sub 3}) {center_dot} xH{sub 2}O{sub (am)}. Like PuO{sub 2(am,hyd)}, Ostwald ripening of Pu(OH){sub 2}(CO{sub 3}){sub (s)} or PuO(CO{sub 3}) {center_dot} xH{sub 2}O{sub (am)} would be expected to occur to produce a more crystalline form of the plutonium carbonate complex. Due to the high alkalinity and low carbonate concentration in the grout formulation, it is expected that upon interaction with the grout, the plutonium carbonate complexes will transform back into plutonium hydroxide. Although crystalline plutonium dioxide is the more stable thermodynamic state of Pu(IV), the low temperature and high water content of the waste during the operating and heel removal periods in Tank 18 have limited the transformation of the plutonium into crystalline plutonium dioxide. During the tank closure period of thousands of years, transformation of the plutonium into a more crystalline plutonium dioxide form would be expected. However, the continuing presence of water, reaction with water radiolysis products, and low temperatures will limit the transformation, and will likely maintain an amorphous Pu(OH){sub 4} or PuO{sub 2(am,hyd)} form on the surface of any crystalline plutonium dioxide produced after tank closure. X-ray Absorption Spectroscopic (XAS) measurements of Tank 18 residues are recommended to confirm coordination environments of the plutonium. If the presence of PuO(CO{sub 3}){sub (am,hyd)} is confirmed by XAS, it is recommended that e

  11. GLASS FABRICATION AND PRODUCT CONSISTENCY TESTING OF LANTHANIDE BOROSHILICATE FRIT X COMPOSITION FOR PLUTONIUM DISPOSITION

    SciTech Connect (OSTI)

    Marra, J

    2006-11-21

    The Department of Energy Office of Environmental Management (DOE/EM) plans to conduct the Plutonium Disposition Project at the Savannah River Site (SRS) to disposition excess weapons-usable plutonium. A plutonium glass waste form is the preferred option for immobilization of the plutonium for subsequent disposition in a geologic repository. A reference glass composition (Lanthanide Borosilicate (LaBS) Frit B) was developed during the Plutonium Immobilization Program (PIP) to immobilize plutonium in the late 1990's. A limited amount of performance testing was performed on this baseline composition before efforts to further pursue Pu disposition via a glass waste form ceased. Recent FY05 studies have further investigated the LaBS Frit B formulation as well as development of a newer LaBS formulation denoted as LaBS Frit X. The objectives of this present task were to fabricate plutonium loaded LaBS Frit X glass and perform corrosion testing to provide near-term data that will increase confidence that LaBS glass product is suitable for disposal in the Yucca Mountain Repository. Specifically, testing was conducted in an effort to provide data to Yucca Mountain Project (YMP) personnel for use in performance assessment calculations. Plutonium containing LaBS glass with the Frit X composition with a 9.5 wt% PuO{sub 2} loading was prepared for testing. Glass was prepared to support Product Consistency Testing (PCT) at Savannah River National Laboratory (SRNL). The glass was thoroughly characterized using x-ray diffraction (XRD) and scanning electron microscopy coupled with energy dispersive spectroscopy (SEM/EDS) prior to performance testing. A series of PCTs were conducted at SRNL using quenched Pu Frit X glass with varying exposed surface areas. Effects of isothermal and can-in-canister heat treatments on the Pu Frit X glass were also investigated. Another series of PCTs were performed on these different heat-treated Pu Frit X glasses. Leachates from all these PCTs were analyzed to determine the dissolved concentrations of key elements. Acid stripping of leach vessels was performed to determine the concentration of the glass constituents that may have sorbed on the vessels during leach testing. Additionally, the leachate solutions were ultrafiltered to quantify colloid formation. Characterization of the quenched Pu Frit X glass prior to testing revealed that some crystalline plutonium oxide was present in the glass. The crystalline particles had a disklike morphology and likely formed via coarsening of particles in areas compositionally enriched in plutonium. Similar results had also been observed in previous Pu Frit B studies. Isothermal 1250 C heat-treated Pu Frit X glasses showed two different crystalline phases (PuO{sub 2} and Nd{sub 2}Hf{sub 2}O{sub 7}), as well as a peak shift in the XRD spectra that is likely due to a solid solution phase PuO{sub 2}-HfO{sub 2} formation. Micrographs of this glass showed a clustering of some of the crystalline phases. Pu Frit X glass subjected to the can-in-canister heating profile also displayed the two PuO{sub 2} and Nd{sub 2}Hf{sub 2}O{sub 7} phases from XRD analysis. Additional micrographs indicate crystalline phases in this glass were of varying forms (a spherical PuO{sub 2} phase that appeared to range in size from submicron to {approx}5 micron, a dendritic-type phase that was comprised of mixed lanthanides and plutonium, and a minor phase that contained Pu and Hf), and clustering of the phases was also observed.

  12. Chancellor Water Colloids: Characterization and Radionuclide Association

    SciTech Connect (OSTI)

    Abdel-Fattah, Amr I.

    2012-06-18

    Concluding remarks about this paper are: (1) Gravitational settling, zeta potential, and ultrafiltration data indicate the existence of a colloidal phase of both the alpha and beta emitters in the Chancellor water; (2) The low activity combined with high dispersion homogeneity of the Chancellor water indicate that both alpha and beta emitters are not intrinsic colloids; (3) Radionuclides in the Chancellor water, particularly Pu, coexist as dissolved aqueous and sorbed phases - in other words the radionuclides are partitioned between the aqueous phase and the colloidal phase; (4) The presence of Pu as a dissolved species in the aqueous phase, suggests the possibility of Pu in the (V) oxidation state - this conclusion is supported by the similarity of the k{sub d} value of Pu determined in the current study to that determined for Pu(V) sorbed onto smectite colloids, and the similar electrokinetic behavior of the Chancellor water colloids to smectite colloids; (5) About 50% of the Pu(V) is in the aqueous phase and 50% is sorbed on colloids (mass concentration of colloids in the Chancellor water is 0.12 g/L); (6) The k{sub d} of the Pu and the beta emitters (fission products) between aqueous and colloidal phases in the Chancellor water is {approx}8.0 x 10{sup 3} mL/g using two different activity measurement techniques (LSC and alpha spectroscopy); (7) The gravitational settling and size distributions of the association colloids indicate that the properties (at least the physical ones) of the colloids to which the alpha emitters are associated with seem to be different that the properties of the colloids to which the beta emitters are associated with - the beta emitters are associated with very small particles ({approx}50 - 120 nm), while the alpha emitters are associated with relatively larger particles; and (8) The Chancellor water colloids are extremely stable under the natural pH and ionic strength conditions, indicating high potential for transport in the subsurface.

  13. Evaluation of technologies for volume reduction of plutonium-contaminated soils from the Nevada Test Site

    SciTech Connect (OSTI)

    Papelis, C.; Jacobson, R.L.; Miller, F.L.; Shaulis, L.K.

    1996-06-01

    Nuclear testing at and around the Nevada Test Site (NTS) resulted in plutonium (Pu) contamination of the soil over an area of several thousands of acres. The objective of this project was to evaluate the potential of five different processes to reduce the volume of Pu-contaminated soil from three different areas, namely Areas 11, 13, and 52. Volume reduction was to be accomplished by concentrating the Pu into a small but highly contaminated soil fraction, thereby greatly reducing the volume of soil requiring disposal. The processes tested were proposed by Paramag Corp. (PARAMAG), Advanced Processing Technologies Inc. (APT), Lockheed Environmental Systems and Technologies (LESAT), Nuclear Remediation Technologies (NRT), and Scientific Ecology Group (SEG). Because of time and budgetary restraints, the NRT and SEG processes were tested with soil from Area 11 only. These processes typically included a preliminary soil conditioning step (e.g., attrition scrubbing, wet sieving), followed by a more advanced process designed to separate Pu from the soil, based on physiochemical properties of Pu compounds (e.g., magnetic susceptibility, specific gravity). Analysis of the soil indicates that a substantial fraction of the total Pu contamination is typically confined in a relatively narrow and small particle size range. Processes which were able to separate this highly contaminated soil fraction (using physical methods, e.g., attrition scrubbing, wet sieving), from the rest of the soil achieved volume (mass) reductions on the order of 70%. The advanced, more complex processes tested did not enhance volume reduction. The primary reason why processes that rely on the dependence of settling velocity on density differences failed was the very fine grain size of the Pu-rich particles.

  14. Transmutation of high-level radioactive waste and production of {sup 233}U using an accelerator-driven reactor

    SciTech Connect (OSTI)

    Takahashi, Hiroshi; Takashita, Hirofumi; Chen, Xinyi

    1994-08-01

    Reactor safety, the disposal of high-level nuclear waste, and nonproliferation of nuclear material for military purposes are the problems of greatest concern for nuclear energy. Technologies for accelerators developed in the field of high-energy physics can contribute to solving these problems. For reactor safety, especially for that of a Na-cooled fast reactor, the use of an accelerator, even a small one, can enhance the safety using a slightly subcritical reactor. There is growing concern about how we can deal with weapons-grade Pu, and about the large amount of Pu accumulating from the operation of commercial reactors. It has been suggested that this Pu could be incinerated, using the reactor and a proton accelerator. However, because Pu is a very valuable material with future potential for generating nuclear energy, we should consider transforming it into a proliferation-resistant material that cannot be used for making bombs, rather than simply eliminating the Pu. An accelerator-driven fast reactor (700 MWt), run in a subcritical condition, and fueled with MOX can generate {sup 233}U more safely and efficiently than can a critical reactor. We evaluate the production of {sup 233}U, {sup 239}Pu, and the transmutation of the long-lived fission products of {sup 99}Tc and {sup 129}I, which are loaded with YH{sub 1.7} between the fast core and blanket, by reducing the conversion factor of Pu to {sup 233}U. And we assessed the rates of radiation damage, hydrogen production, and helium production in a target window and in the surrounding vessel.

  15. DISTRIBUTION OF ACTINIDES BETWEEN THE AQUEOUS AND ORGANIC PHASES IN THE TALSPEAK PROCESS

    SciTech Connect (OSTI)

    Rudisill, T.; Kyser, E.

    2010-09-02

    One objective of the US Department of Energy's Office of Nuclear Energy (DOE-NE) is the development of sustainable nuclear fuel cycles which improve uranium resource utilization, maximize energy generation, minimize waste generation, improve safety, and complement institutional measures limiting proliferation risks. Activities in progress which support this objective include the development of advanced separation technologies to recover the actinides from used nuclear fuels. With the increased interest in the development of technology to allow closure of the nuclear fuel cycle, the TALSPEAK process is being considered for the separation of Am and Cm from the lanthanide fission products in a next generation reprocessing plant. However, at this time, the level of understanding associated with the chemistry and the control of the process variables is not acceptable for deployment of the process on an industrial scale. To address this issue, DOE-NE is supporting basic scientific studies focused on the TALSPEAK process through its Fuel Cycle Research and Development (R&D) program. One aspect of these studies is an experimental program at the Savannah River National Laboratory (SRNL) in which temperature-dependent distribution coefficients for the extraction of actinide elements in the TALSPEAK process were measured. The data were subsequently used to calculate conditional enthalpies and entropies of extraction by van't Hoff analysis to better understand the thermodynamic driving forces for the TALSPEAK process. In the SRNL studies, the distribution of Pu(III) in the TALSPEAK process was of particular interest. A small amount of Pu(III) would be present in the feed due to process losses and valence adjustment in prior recovery operations. Actinide elements such as Np and Pu have multiple stable oxidation states in aqueous solutions; therefore the oxidation state for these elements must be controlled in the TALSPEAK process, as the extraction chemistry is dependent upon the actinide's valence. Since our plans included the measurement of Pu(III) distribution coefficients using a Np(V) solution containing small amounts of {sup 238}Pu, it was necessary to demonstrate that the desired oxidation states of Np and Pu are produced and could be stabilized in a buffered lactate solution containing diethylenetriaminepentaacetic (DTPA). The stability of Np(V) and Pu(III) in lactic acid/DTPA solutions was evaluated by ultraviolet-visible (UV-vis) spectroscopy. To perform the evaluation, Np and Pu were added to solutions containing either hydroxylamine nitrate (HAN) or ferrous sulfamate (FS) as the reductant and nominally 1.5 M lactic acid/0.05 M DTPA. The pH of the solution was subsequently adjusted to nominally 2.8 as would be performed in the TALSPEAK process. In the valence adjustment study, we found that it was necessary to reduce Pu to Pu(III) prior to combining with the lactic acid and DTPA. The Pu reduction was performed using either HAN or FS. When FS was used, Np was reduced to Np(IV). The spectroscopic studies showed that Np(V) and Pu(III) are not stable in lactic acid/DTPA solutions. The stability of Np(IV)- and Pu(IV)-DTPA complexes are much greater than the stability of the Np(V)- and Pu(III)-DTPA complexes, and as a result, Np is slowly reduced to Np(IV) and Pu is slowly oxidized to Pu(IV) due to the reduced activity of the more stable complexes. When Np(V) was added to a solution containing a 1.5 M lactic acid/ammonium lactate buffer and 0.05 M DTPA, approximately 50% of the Np was reduced to Np(IV) in the first day. The fraction of Np(V) in the solution continued to diminish with time and was essentially reduced to Np(IV) after one week. When Pu(III) was added to a lactic acid/DTPA solution of the same composition, the spectrum recorded following at least two days after preparation of the solution continued to show some sign of Pu(III). The Pu(III) was completely oxidized to Pu(IV) after 3-4 days. The UV-vis spectroscopy demonstrated that Np(V) and Pu(III) were the predominate valences in the lactic acid/DTPA solution for th

  16. DISSOLUTION OF PLUTONIUM METAL IN 8-10 M NITRIC ACID

    SciTech Connect (OSTI)

    Rudisill, T.; Pierce, R.

    2012-02-21

    The H-Canyon facility will be used to dissolve Pu metal for subsequent purification and conversion to plutonium dioxide (PuO{sub 2}) using Phase II of HB-Line. To support the new mission, the development of a Pu metal dissolution flowsheet which utilizes concentrated (8-10 M) nitric acid (HNO{sub 3}) solutions containing potassium fluoride (KF) is required. Dissolution of Pu metal in concentrated HNO{sub 3} is desired to eliminate the need to adjust the solution acidity prior to purification by anion exchange. The preferred flowsheet would use 8-10 M HNO{sub 3}, 0.015-0.07 M KF, and 0.5-1.0 g/L Gd to dissolve the Pu up to 6.75 g/L. An alternate flowsheet would use 8-10 M HNO{sub 3}, 0.1-0.2 M KF, and 1-2 g/L B to dissolve the Pu. The targeted average Pu metal dissolution rate is 20 mg/min-cm{sup 2}, which is sufficient to dissolve a 'standard' 2250-g Pu metal button in 24 h. Plutonium metal dissolution rate measurements showed that if Gd is used as the nuclear poison, the optimum dissolution conditions occur in 10 M HNO{sub 3}, 0.04-0.05 M KF, and 0.5-1.0 g/L Gd at 112 to 116 C (boiling). These conditions will result in an estimated Pu metal dissolution rate of {approx}11-15 mg/min-cm{sup 2} and will result in dissolution times of 36-48 h for standard buttons. The recommended minimum and maximum KF concentrations are 0.03 M and 0.07 M, respectively. The maximum KF concentration is dictated by a potential room-temperature Pu-Gd-F precipitation issue at low Pu concentrations. The purpose of the experimental work described in this report was two-fold. Initially a series of screening experiments was performed to measure the dissolution rate of Pu metal as functions of the HNO{sub 3}, KF, and Gd or B concentrations. The objective of the screening tests was to propose optimized conditions for subsequent flowsheet demonstration tests. Based on the rate measurements, this study found that optimal dissolution conditions in solutions containing 0.5-1.0 g/L Gd occurred in 8-10 M HNO{sub 3} with 0.04-0.05 M KF at 112 to 116 C (boiling). The testing also showed that solutions containing 8-10 M HNO{sub 3}, 0.1-0.2 M KF, and 1-2 g/L B achieved acceptable dissolution rates in the same temperature range. To confirm that conditions identified by the dissolution rate measurements for solutions containing Gd or B can be used to dissolve Pu metal up to 6.75 g/L in the presence of Fe, demonstration experiments were performed using concentrations in the optimal ranges. In two of the demonstration experiments using Gd and in one experiment using B, the offgas generation during the dissolution was measured and samples were analyzed for H{sub 2}. The experimental methods used to perform the dissolution rate measurements and flowsheet demonstrations and a discussion of the results are presented.

  17. TECHNICAL BASIS FOR DOE STANDARD 3013 EQUIVALENCY SUPPORTING REDUCED TEMPERATURE STABILIZATION OF OXALATE-DERIVED PLUTONIUM OXIDE PRODUCED BY THE HB-LINE FACILITY AT SAVANNAH RIVER SITE

    SciTech Connect (OSTI)

    Duffey, J.; Livingston, R.; Berg, J.; Veirs, D.

    2012-07-02

    The HB-Line (HBL) facility at the Savannah River Site (SRS) is designed to produce high-purity plutonium dioxide (PuO{sub 2}) which is suitable for future use in production of Mixed Oxide (MOX) fuel. The MOX Fuel Fabrication Facility (MFFF) requires PuO{sub 2} feed to be packaged per the U.S. Department of Energy (DOE) Standard 3013 (DOE-STD-3013) to comply with the facility's safety basis. The stabilization conditions imposed by DOE-STD-3013 for PuO{sub 2} (i.e., 950 C for 2 hours) preclude use of the HBL PuO{sub 2} in direct fuel fabrication and reduce the value of the HBL product as MFFF feedstock. Consequently, HBL initiated a technical evaluation to define acceptable operating conditions for production of high-purity PuO{sub 2} that fulfills the DOE-STD-3013 criteria for safe storage. The purpose of this document is to demonstrate that within the defined operating conditions, the HBL process will be equivalent for meeting the requirements of the DOE-STD-3013 stabilization process for plutonium-bearing materials from the DOE complex. The proposed 3013 equivalency reduces the prescribed stabilization temperature for high-purity PuO{sub 2} from oxalate precipitation processes from 950 C to 640 C and places a limit of 60% on the relative humidity (RH) at the lowest material temperature. The equivalency is limited to material produced using the HBL established flow sheet, for example, nitric acid anion exchange and Pu(IV) direct strike oxalate precipitation with stabilization at a minimum temperature of 640 C for four hours (h). The product purity must meet the MFFF acceptance criteria of 23,600 {micro}g/g Pu (i.e., 2.1 wt %) total impurities and chloride content less than 250 {micro}g/g of Pu. All other stabilization and packaging criteria identified by DOE-STD-3013-2012 or earlier revisions of the standard apply. Based on the evaluation of test data discussed in this document, the expert judgment of the authors supports packaging the HBL product under a 3013 equivalency. Under the defined process conditions and associated material specifications, the high-purity PuO{sub 2} produced in HBL presents no unique safety concerns for packaging or storage in the 3013 required configuration. The PuO{sub 2} produced using the HBL flow sheet conditions will have a higher specific surface area (SSA) than PuO{sub 2} stabilized at 950 C and, consequently, under identical conditions will adsorb more water from the atmosphere. The greatest challenge to HBL operators will be controlling moisture content below 0.5 wt %. However, even at the 0.5 wt % moisture limit, the maximum acceptable pressure of a stoichiometric mixture of hydrogen and oxygen in the 3013 container is greater than the maximum possible pressure for the HBL PuO{sub 2} product.

  18. ANALYSIS OF 2H-EVAPORATOR SCALE WALL [HTF-13-82] AND POT BOTTOM [HTF-13-77] SAMPLES

    SciTech Connect (OSTI)

    Oji, L.

    2013-06-21

    Savannah River Remediation (SRR) is planning to remove a buildup of sodium aluminosilicate scale from the 2H-evaporator pot by loading and soaking the pot with heated 1.5 M nitric acid solution. Sampling and analysis of the scale material has been performed so that uranium and plutonium isotopic analysis can be input into a Nuclear Criticality Safety Assessment (NCSA) for scale removal by chemical cleaning. Historically, since the operation of the Defense Waste Processing Facility (DWPF), silicon in the DWPF recycle stream combines with aluminum in the typical tank farm supernate to form sodium aluminosilicate scale mineral deposits in the 2Hevaporator pot and gravity drain line. The 2H-evaporator scale samples analyzed by Savannah River National Laboratory (SRNL) came from the bottom cone sections of the 2H-evaporator pot [Sample HTF-13-77] and the wall 2H-evaporator [sample HTF-13-82]. X-ray diffraction analysis (XRD) confirmed that both the 2H-evaporator pot scale and the wall samples consist of nitrated cancrinite (a crystalline sodium aluminosilicate solid) and clarkeite (a uranium oxy-hydroxide mineral). On “as received” basis, the bottom pot section scale sample contained an average of 2.59E+00 ± 1.40E-01 wt % total uranium with a U-235 enrichment of 6.12E-01 ± 1.48E-02 %, while the wall sample contained an average of 4.03E+00 ± 9.79E-01 wt % total uranium with a U-235 enrichment of 6.03E-01% ± 1.66E-02 wt %. The bottom pot section scale sample analyses results for Pu-238, Pu-239, and Pu-241 are 3.16E- 05 ± 5.40E-06 wt %, 3.28E-04 ± 1.45E-05 wt %, and <8.80E-07 wt %, respectively. The evaporator wall scale samples analysis values for Pu-238, Pu-239, and Pu-241 averages 3.74E-05 ± 6.01E-06 wt %, 4.38E-04 ± 5.08E-05 wt %, and <1.38E-06 wt %, respectively. The Pu-241 analyses results, as presented, are upper limit values. These results are provided so that SRR can calculate the equivalent uranium-235 concentrations for the NCSA. Results confirm that the uranium contained in the scale remains depleted with respect to natural uranium. SRNL did not calculate an equivalent U-235 enrichment, which takes into account other fissionable isotopes U-233, Pu-239 and Pu-241. The applicable method for calculation of equivalent U-235 will be determined in the NCSA.

  19. In-situ gamma-ray assay of the east cell line in the 235-F Plutonium fuel form facility

    SciTech Connect (OSTI)

    Diprete, D.

    2015-08-21

    On September 17th -19th , 2013, scientists from SRNL took a series of in-situ gamma-ray measurements in the maintenance trench beneath Cells 1-5 on the east line of the PuFF facility using a well-collimated, high-purity germanium detector. The cell interiors were assayed along with the furnaces and storage coolers that protrude beneath the cells. The detector efficiency was estimated using a combination of MCNP simulations and empirical measurements. Data analysis was performed using three gamma-rays emitted by Pu-238 (99.85 keV, 152.7 keV, and 766.4 keV) providing three independent estimates of the mass of Pu-238 holdup in each of the cells. The weighted mean of these three results was used as the best estimate of Pu-238 holdup in the East Cell Line of PuFF. The results of the assay measurements are found in the table on the following page along with the results from the scoping assay performed in 2006. All uncertainties in this table (as well as the rest of the report) are reported at 1?. Summing the assay results and treating MDAs as M238Pu= 0 ± MDA, the total holdup in the East Cell Line was 240 ± 40 grams. This result is 100 grams lower than the previous estimate, a 0.55? difference. The uncertainty in the Pu-238 holdup is also reduced substantially relative to the 2006 scoping assay. However, the current assay results are in agreement with the 2006 scoping assay results due to the large uncertainty associated with the 2006 scoping assays. The current assay results support the conclusion that the 2006 results bound the Pu-238 mass in Cells 1-5. These results should be considered preliminary since additional measurements of the East Cell line are scheduled for 2017 and 2018. Those measurements will provide detailed information about the distribution of Pu-238 in the cells to be used to refine the results of the current assay.

  20. Concordant plutonium-241-americium-241 dating of environmental samples: results from forest fire ash

    SciTech Connect (OSTI)

    Goldstein, Steven J; Oldham, Warren J; Murrell, Michael T; Katzman, Danny

    2010-12-07

    We have measured the Pu, {sup 237}Np, {sup 241}Am, and {sup 151}Sm 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 {sup 241}Pu (t{sub 1/2} = 14.4 y)-{sup 241}Am 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 {sup 242}/{sup 239}Pu as a normalizing isotope ratio in a three-isotope plot, where this ratio for the nonglobal 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, {sup 151}Sm (t{sub 1/2} = 90 y). We find that forest fire ash concentrates actinides and fission products with {approx}1E10 atoms {sup 239}Pu/g and {approx}1E8 atoms {sup 151}Sm/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 {sup 151}Sm 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 {sup 151}Sm/{sup 239}Pu atom ratio for global fallout is {approx}0.164, in agreement with an independent estimate of 0.165 based on {sup 137}Cs fission yields for atmospheric weapons tests at the NTS. {sup 241}Pu-{sup 241}Am 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 {sup 242}Pu and {sup 151}Sm normalizations, although the errors for the {sup 151}Sm correction are currently larger due to the greater uncertainty of their measurements. Additional efforts to develop a concordant {sup 241}Pu-{sup 241}Am dating method for environmental collections are underway with emphasis on soil cores.

  1. Decontamination Techniques and Fixative Coatings Evaluated in the Building 235-F Legacy Source Term Removal Study

    SciTech Connect (OSTI)

    WAYNE, FARRELL

    2005-04-21

    Savannah River Site Building 235-F was being considered for future plutonium storage and stabilization missions but the Defense Nuclear Facilities Safety Board (DNFSB) noted that large quantities of Plutonium-238 left in cells and gloveboxes from previous operations posed a potential hazard to both the existing and future workforce. This material resulted from the manufacture of Pu-238 heat sources used by the NASA space program to generate electricity for deep space exploration satellites. A multi-disciplinary team was assembled to propose a cost- effective solution to mitigate this legacy source term which would facilitate future DOE plutonium storage activities in 235-F. One aspect of this study involved an evaluation of commercially available radiological decontamination techniques to remove the legacy Pu-238 and fixative coatings that could stabilize any residual Pu-238 following decontamination activities. Four chemical methods were identified as most likely to meet decontamination objectives for this project and are discussed in detail. Short and long term fixatives will be reviewed with particular attention to the potential radiation damage caused by Pu-238, which has a high specific activity and would be expected to cause significant radiation damage to any coating applied. Encapsulants that were considered to mitigate the legacy Pu-238 will also be reviewed.

  2. Radionuclide Concentration in Soils and Vegetation at Low-Level Radioactive Waste Disposal Area G during 2005

    SciTech Connect (OSTI)

    P.R. Fresquez; M.W. McNaughton; M.J. Winch

    2005-10-01

    Soil samples were collected at 15 locations and unwashed overstory and understory vegetation samples were collected from up to nine locations within and around the perimeter of Area G, the primary disposal facility for low-level radioactive solid waste at Los Alamos National Laboratory (LANL). Soil and plant samples were also collected from the proposed expansion area west of Area G for the purpose of gaining preoperational baseline data. Soil and plant samples were analyzed for radionuclides that have shown a history of detection in past years; these included {sup 3}H, {sup 238}Pu, {sup 239,240}Pu, {sup 241}Am, {sup 234}U, {sup 235}U, and {sup 238}U for soils and {sup 3}H, {sup 238}Pu, and {sup 239,240}Pu for plants. As in previous years, the highest levels of {sup 3}H in soils and vegetation were detected at the south portion of Area G near the {sup 3}H shafts; whereas, the highest concentrations of the Pu isotopes were detected in the northern and northeastern portions near the pads for transuranic waste. All concentrations of radionuclides in soils and vegetation, however, were still very low (pCi range) and far below LANL screening levels and regulatory standards.

  3. In-situ gamma-ray assay of the west cell line in the 235-F plutonium fuel form facility

    SciTech Connect (OSTI)

    Couture, A. H.; Diprete, D.

    2014-09-01

    On August 29th, 2013, scientists from SRNL took a series of in-situ gamma-ray measurements in the maintenance trench beneath Cells 6-9 on the west line of the PuFF facility using an uncollimated, highpurity germanium detector. The detector efficiency was estimated using a combination of MCNP simulations and empirical measurements. Data analysis was performed using three gamma-rays emitted by Pu-238 (99.85 keV, 152.7 keV, and 766.4 keV) providing three independent estimates of the mass of Pu-238 holdup in each of the cells. The weighted mean of these three results was used as the best estimate of Pu-238 holdup in the West Cell Line of PuFF. The results of the assay measurements are found in the table below along with the results from the scoping assay performed in 2006. All uncertainties in this table (as well as the rest of the report) are given as 1?. The total holdup in the West Cell Line was 2.4 ± 0.7 grams. This result is 0.6 g higher than the previous estimate, a 0.4? difference.

  4. Ab Initio Enhanced calphad Modeling of Actinide-Rich Nuclear Fuels

    SciTech Connect (OSTI)

    Morgan, Dane; Yang, Yong Austin

    2013-10-28

    The process of fuel recycling is central to the Advanced Fuel Cycle Initiative (AFCI), where plutonium and the minor actinides (MA) Am, Np, and Cm are extracted from spent fuel and fabricated into new fuel for a fast reactor. Metallic alloys of U-Pu-Zr-MA are leading candidates for fast reactor fuels and are the current basis for fast spectrum metal fuels in a fully recycled closed fuel cycle. Safe and optimal use of these fuels will require knowledge of their multicomponent phase stability and thermodynamics (Gibbs free energies). In additional to their use as nuclear fuels, U-Pu-Zr-MA contain elements and alloy phases that pose fundamental questions about electronic structure and energetics at the forefront of modern many-body electron theory. This project will validate state-of-the-art electronic structure approaches for these alloys and use the resulting energetics to model U-Pu-Zr-MA phase stability. In order to keep the work scope practical, researchers will focus on only U-Pu-Zr-{Np,Am}, leaving Cm for later study. The overall objectives of this project are to: Provide a thermodynamic model for U-Pu-Zr-MA for improving and controlling reactor fuels; and, Develop and validate an ab initio approach for predicting actinide alloy energetics for thermodynamic modeling.

  5. Supercritical Fluid Extraction of Plutonium and Americium from Soil using Thenoyltrifluoroacetone and Tributylphosphate Complexation

    SciTech Connect (OSTI)

    Mincher, Bruce Jay; Fox, Robert Vincent; Holmes, R.; Robbins, R; Boardman, C.

    2001-10-01

    Samples of clean soil from the source used to backfill pits at the Idaho National Engineering and Environmental Laboratory's Radioactive Waste Management Complex were spiked with Pu-239 and Am-241 to evaluate ligand-assistedsupercritical fluid extraction as a decontamination method. The actual soil in the pits has been subject to approximately three decades of weatheringsince it was originally contaminated. No surrogate soil can perfectly simulate the real event, but actual contaminated soil was not available for research purposes. However, fractionation of Am and Pu in the surrogate soil was found to be similar to that previously measured in the real soil using asequential aqueous extraction procedure. This suggests that Pu and Am behavior are similar in the two soils. The surrogate was subjected to supercritical carbon dioxide extraction, in the presence of the fluorinated beta diketone thenoyltrifluoroacetone (TTA), and tributylphosphate (TBP). As much as 69% of the Pu and 88% of the Am were removed from the soil using 3.2mol% TTA and 2.7 mol % TBP, in a single 45 minute extraction. Extraction conditions employing a 5 mol % ethanol modifier with 0.33 mol % TTA and 0.27 mol %TBP resulted in 66% Pu and 68% Am extracted. To our knowledge, this is thefirst report of the use of supercritical fluid extraction (SFE) for the removal of actinides from soil.

  6. Specific sequestering agents for actinides. 11. Complexation of plutonium and americium by catecholate ligands

    SciTech Connect (OSTI)

    Kappel, M.J.; Nitsche, H.; Raymond, N.N.

    1985-02-13

    The results of the first in vitro experiments regarding the complexation of plutonium and americium by catechol and tetracatechoylamide ligands are presented. Electrochemical techniques have allowed the elucidation of the protonation behavior of Pu(IV)-and Pu(III)-catecholate complexes. Above pH 12, the Pu(IV) complex is a tetrakis(catecholate) complex and the Pu(III) complex is a tetrakis- or tris(catecholate) complex, depending upon ligand concentration. At neutral pH, the Pu(IV) complex of the octadentate ligand 3,4,3-LICAMS appears to be a tris(catecholate) complex, indicating that the full denticity of the ligand is not utilized in vivo. Spectroscopic evidence is presented for the complexation of Am(III) by tetracatechoylamide ligands. The inability to observe the Am(IV)/Am(III)-catecholate reduction couple indicates that the free-ion Am(IV)/Am(III) reduction potential is greater than +2.6 V vs. NHE. 48 references, 9 figures, 2 tables.

  7. First AID (Atom counting for Isotopic Determination).

    SciTech Connect (OSTI)

    Roach, J. L. (Jeffrey L.); Israel, K. M. (Kimberly M.); Steiner, R. E. (Robert E.); Duffy, C. J. (Clarence J.); Roench, F. R. (Fred R.)

    2002-01-01

    Los Alamos National Laboratory (LANL) has established an in vitro bioassay monitoring program in compliance with the requirements in the Code of Federal Regulations, 10 CFR 835, Occupational Radiation Protection. One aspect of this program involves monitoring plutonium levels in at-risk workers. High-risk workers are monitored using the ultra-sensitive Therrnal Ionization Mass Spectrometry (TIMS) technique to ensure compliance with DOE standards. TIMS is used to measure atom ratios of 239Pua nd 240Puw ith respect to a tracer isotope ('Pu). These ratios are then used to calculate the amount of 239Pu and 240Pup resent. This low-level atom counting technique allows the calculation of the concentration levels of 239Pu and 240Pu in urine for at risk workers. From these concentration levels, dose assessments can be made and worker exposure levels can be monitored. Detection limits for TIMS analysis are on the order of millions of atoms, which translates to activity levels of 150 aCi 239Pua nd 500 aCi for 240Pu. pCi for Our poster presentation will discuss the ultra-sensitive, low-level analytical technique used to measure plutonium isotopes and the data verification methods used for validating isotopic measurements.

  8. Carrier-mediated transport of actinide ions using supported liquid membranes containing TODGA as the carrier extractant

    SciTech Connect (OSTI)

    Panja, S.; Dakshinamoorthy, A.; Munshi, S.K.; Dey, P.K.; Mohapatra, P.K.; Manchanda, V.K.

    2008-07-01

    The transport behavior of Pu{sup 3+} under varying reducing conditions was investigated from a feed containing 3.0 M HNO{sub 3} into a receiver phase containing 0.1 M HNO{sub 3} using TODGA (N,N,N',N' - tetraoctyl-diglycolamide) as the carrier ligand. A mixture of 0.2 M hydroxyl ammonium nitrate and 0.2 M hydrazinium nitrate (used in the feed as the reducing agent) has been found to be effective for quantitative (>99%) transport of the trivalent Pu in about 3 h. Transport of trivalent plutonium in 3 h (>99%) was higher as compared to that of the tetravalent plutonium (94%), though their D values followed an opposite trend. The permeability coefficient (P) of Pu{sup 3+} was (4.63 {+-} 0.26) x 10{sup -3} cm/s as compared to (2.10 {+-} 0.14) x 10{sup -3} cm/s for Pu{sup 4+} and (3.67 {+-} 0.06) x 10{sup -3} cm/s Am{sup 3+}. P values of trivalent actinide ions such as Am{sup 3+}, Pu{sup 3+}, and Cm{sup 3+} are compared with their distribution data. (authors)

  9. Plutonium Detection with Straw Neutron Detectors

    SciTech Connect (OSTI)

    Mukhopadhyay, Sanjoy; Maurer, Richard; Guss, Paul

    2014-03-27

    A kilogram of weapons grade plutonium gives off about 56,000 neutrons per second of which 55,000 neutrons come from spontaneous fission of 240Pu (~6% by weight of the total plutonium). Actually, all even numbered isotopes (238Pu, 240Pu, and 242Pu) produce copious spontaneous fission neutrons. These neutrons induce fission in the surrounding fissile 239Pu with an approximate multiplication of a factor of ~1.9. This multiplication depends on the shape of the fissile materials and the surrounding material. These neutrons (typically of energy 2 MeV and air scattering mean free path >100 meters) can be detected 100 meters away from the source by vehicle-portable neutron detectors. [1] In our current studies on neutron detection techniques, without using 3He gas proportional counters, we designed and developed a portable high-efficiency neutron multiplicity counter using 10B-coated thin tubes called straws. The detector was designed to perform like commercially available fission meters (manufactured by Ortec Corp.) except instead of using 3He gas as a neutron conversion material, we used a thin coating of 10B.

  10. Spent nuclear fuel recycling with plasma reduction and etching

    DOE Patents [OSTI]

    Kim, Yong Ho

    2012-06-05

    A method of extracting uranium from spent nuclear fuel (SNF) particles is disclosed. Spent nuclear fuel (SNF) (containing oxides of uranium, oxides of fission products (FP) and oxides of transuranic (TRU) elements (including plutonium)) are subjected to a hydrogen plasma and a fluorine plasma. The hydrogen plasma reduces the uranium and plutonium oxides from their oxide state. The fluorine plasma etches the SNF metals to form UF6 and PuF4. During subjection of the SNF particles to the fluorine plasma, the temperature is maintained in the range of 1200-2000 deg K to: a) allow any PuF6 (gas) that is formed to decompose back to PuF4 (solid), and b) to maintain stability of the UF6. Uranium (in the form of gaseous UF6) is easily extracted and separated from the plutonium (in the form of solid PuF4). The use of plasmas instead of high temperature reactors or flames mitigates the high temperature corrosive atmosphere and the production of PuF6 (as a final product). Use of plasmas provide faster reaction rates, greater control over the individual electron and ion temperatures, and allow the use of CF4 or NF3 as the fluorine sources instead of F2 or HF.

  11. Reactor physics studies for assessment of tramp uranium methods

    SciTech Connect (OSTI)

    Grimm, P.; Vasiliev, A.; Wieselquist, W.; Ferroukhi, H.; Ledergerber, G.

    2012-07-01

    This paper presents calculation studies towards validation of a methodology for estimations of the tramp uranium mass from water chemistry measurements. Particular emphasis is given to verify, from a reactor physics point of view, the justification basis for the so-called 'Pu-based model' versus the 'U-based model' as a key assumption for the methodology. The computational studies are carried out for a typical BWR fuel assembly with CASMO-5M and MCNPX. By approximating the evolution of fissile nuclides and the fraction of {sup 235}U fissions to total fissions in different zones of a fuel rod, including tramp uranium on the clad surface, it is found that Pu gives the dominant contribution to fissions for tramp uranium after an irradiation on the outer clad surface of at least one cycle in a BWR. Thus, the use of the so-called Pu model for the determination of the tramp uranium mass (this means in particular using the yields for {sup 239}Pu fission) appears justified in the cases considered. On that basis, replacing the older U model by a Pu model is recommended. (authors)

  12. Processing of Non-PFP Plutonium Oxide in Hanford Plants

    SciTech Connect (OSTI)

    Jones, Susan A.; Delegard, Calvin H.

    2011-03-10

    Processing of non-irradiated plutonium oxide, PuO2, scrap for recovery of plutonium values occurred routinely at Hanford’s Plutonium Finishing Plant (PFP) in glovebox line operations. Plutonium oxide is difficult to dissolve, particularly if it has been high-fired; i.e., calcined to temperatures above about 400°C and much of it was. Dissolution of the PuO2 in the scrap typically was performed in PFP’s Miscellaneous Treatment line using nitric acid (HNO3) containing some source of fluoride ion, F-, such as hydrofluoric acid (HF), sodium fluoride (NaF), or calcium fluoride (CaF2). The HNO3 concentration generally was 6 M or higher whereas the fluoride concentration was ~0.5 M or lower. At higher fluoride concentrations, plutonium fluoride (PuF4) would precipitate, thus limiting the plutonium dissolution. Some plutonium-bearing scrap also contained PuF4 and thus required no added fluoride. Once the plutonium scrap was dissolved, the excess fluoride was complexed with aluminum ion, Al3+, added as aluminum nitrate, Al(NO3)3•9H2O, to limit collateral damage to the process equipment by the corrosive fluoride. Aluminum nitrate also was added in low quantities in processing PuF4.

  13. Comparative behavior of plutonium and americium in the equatorial Pacific

    SciTech Connect (OSTI)

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

    1983-01-01

    Inventories of /sup 239 +240/Pu and /sup 241/Am greatly in excess of global fallout levels persist in the benthic environments of Bikini and Enewetak Atolls. The amount of /sup 239 +240/Pu mobilized to solution at the atolls can be predicted from a distribution coefficient K/sub d/ of 2.3 x 10/sup 5/ and the mean sediment concentrations. The mobilized /sup 239 +240/Pu has solute-like characteristics and different valence states coexist in solution - the largest fraction of the soluble plutonium is in an oxidized form (+V,VI). The adsorption of plutonium to sediments is not completely reversible because of changes that occur in the relative amounts of the mixed oxidation states in solution with time. Characteristics of /sup 239 +240/Pu described at one location may not necessarily describe its behavior elsewhere. The relative amounts of /sup 241/Am to /sup 239 +240/Pu may be altered in future years because of mobilization and radiological decay.

  14. Northern Marshall Islands radiological survey: sampling and analysis summary

    SciTech Connect (OSTI)

    Robison, W.L.; Conrado, C.L.; Eagle, R.J.; Stuart, M.L.

    1981-07-23

    A radiological survey was conducted in the Northern Marshall Islands to document reamining external gamma exposures from nuclear tests conducted at Enewetak and Bikini Atolls. An additional program was later included to obtain terrestrial and marine samples for radiological dose assessment for current or potential atoll inhabitants. This report is the first of a series summarizing the results from the terrestrial and marine surveys. The sample collection and processing procedures and the general survey methodology are discussed; a summary of the collected samples and radionuclide analyses is presented. Over 5400 samples were collected from the 12 atolls and 2 islands and prepared for analysis including 3093 soil, 961 vegetation, 153 animal, 965 fish composite samples (average of 30 fish per sample), 101 clam, 50 lagoon water, 15 cistern water, 17 groundwater, and 85 lagoon sediment samples. A complete breakdown by sample type, atoll, and island is given here. The total number of analyses by radionuclide are 8840 for /sup 241/Am, 6569 for /sup 137/Cs, 4535 for /sup 239 +240/Pu, 4431 for /sup 90/Sr, 1146 for /sup 238/Pu, 269 for /sup 241/Pu, and 114 each for /sup 239/Pu and /sup 240/Pu. A complete breakdown by sample category, atoll or island, and radionuclide is also included.

  15. Evolving Density and Static Mechanical Properties in Plutonium from Self-Irradiation

    SciTech Connect (OSTI)

    Chung, B W; Thompson, S R; Lema, K E; Hiromoto, D S; Ebbinghaus, B B

    2008-07-31

    Plutonium, because of its self-irradiation by alpha decay, ages by means of lattice damage and helium in-growth. These integrated aging effects result in microstructural and physical property changes. Because these effects would normally require decades to measure, studies are underway to assess the effects of extended aging on the physical properties of plutonium alloys by incorporating roughly 7.5 weight % of highly specific activity isotope {sup 238}Pu into the {sup 239}Pu metal to accelerate the aging process. This paper presents updated results of self-irradiation effects on {sup 238}Pu-enriched alloys measured by immersion density, dilatometry, and tensile tests. After nearly 90 equivalent years of aging, both the immersion density and dilatometry show that the enriched alloys continue to decreased in density by {approx}0.002% per year, without void swelling. Quasi-static tensile measurements show that the aging process increases the strength of plutonium alloys.

  16. Plutonium-238 alpha-decay damage study of the ceramic waste form.

    SciTech Connect (OSTI)

    Frank, S M [U.S. Department of Energy, Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415; Barber, T L [U.S. Department of Energy, Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415; Cummings, D G [U.S. Department of Energy, Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415; DiSanto, T [U.S. Department of Energy, Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415; Esh, D W [U.S. Nuclear Regulatory Commission, Washington, DC 20555-0001; Giglio, J J [U.S. Department of Energy, Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415; Goff, K M [U.S. Department of Energy, Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415; Johnson, S G [U.S. Department of Energy, Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415; Kennedy, J R [U.S. Department of Energy, Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415; Jue, J-F [U.S. Department of Energy, Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415; Noy, M [U.S. Department of Energy, Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415; O'Holleran, T P [U.S. Department of Energy, Idaho National Laboratory, P.O. Box 1625, Idaho Falls, ID 83415; Sinkler, W [UOP LLC, 25 E Algonquin Road, Des Plaines, IL 60017

    2006-03-27

    An accelerated alpha-decay damage study of a glass-bonded sodalite ceramic waste form has recently been completed. The purpose of this study was to investigate the physical and chemical durability of the waste form after significant exposure to alpha decay. This accelerated alpha-decay study was performed by doping the ceramic waste form with {sup 238}Pu which has a much greater specific activity than {sup 239}Pu that is normally present in the waste form. The alpha-decay dose at the end of the four year study was approximately 1 x 10{sup 18} alpha-decays/gram of material. An equivalent time period for a similar dose of {sup 239}Pu would require approximately 1100 years. After four years of exposure to {sup 238}Pu alpha decay, the investigation observed little change to the physical or chemical durability of the ceramic waste form (CWF). Specifically, the {sup 238}Pu-loaded CWF maintained it's physical integrity, namely that the density remained constant and no cracking or phase de-bonding was observed. The materials chemical durability and phase stability also did not change significantly over the duration of the study. The only significant measured change was an increase of the unit-cell lattice parameters of the plutonium oxide and sodalite phases of the material and an increase in the release of salt components and plutonium of the waste form during leaching tests, but, as mentioned, these did not lead to any overall loss of waste form durability. The principal findings from this study are: (1) {sup 238}Pu-loaded CWF is similar in microstructure and phase composition to referenced waste form. (2) Pu was observed primarily as oxide comprised of aggregates of nano crystals with aggregates ranging in size from submicron to twenty microns in diameter. (3) Pu phases were primarily found in the intergranular glassy regions. (4) PuO phase shows expected unit cell volume expansion due to alpha decay damage of approximately 0.7%, and the sodalite phase unit cell volume has expanded slightly by 0.3% again, presumably due to alpha-decay damage. (5) No bulk sample swelling was observed. (6) No amorphization of sodalite or actinide bearing phases was observed after four years of alpha-decay damage. (7) No microcracks or phase de-bonding were observed in waste form samples aged for four years. (8) In some areas of the {sup 238}Pu doped ceramic waste form material bubbles and voids were found. Bubbles and voids with similar size and density were also found in ceramic waste form samples without actinide. These bubbles and voids are interpreted as pre-existing defects. However, some contribution to these bubbles and voids from helium gas can not be ruled out. (9) Chemical durability of {sup 238}Pu CWF has not changed significantly after four years of alpha-decay exposure except for an increase in the release of salt components and Pu. Still, the plutonium release from CWF is very low at less than 0.005 g/m{sup 2}.

  17. Improved Radiation Dosimetry/Risk Estimates to Facilitate Environmental Management of Plutonium-Contaminated Sites

    SciTech Connect (OSTI)

    Scott, Bobby R.; Tokarskaya, Zoya B.; Zhuntova, Galina V.; Osovets, Sergey V.; Syrchikov, Victor A., Belyaeva, Zinaida D.

    2007-12-14

    This report summarizes 4 years of research achievements in this Office of Science (BER), U.S. Department of Energy (DOE) project. The research described was conducted by scientists and supporting staff at Lovelace Respiratory Research Institute (LRRI)/Lovelace Biomedical and Environmental Research Institute (LBERI) and the Southern Urals Biophysics Institute (SUBI). All project objectives and goals were achieved. A major focus was on obtaining improved cancer risk estimates for exposure via inhalation to plutonium (Pu) isotopes in the workplace (DOE radiation workers) and environment (public exposures to Pu-contaminated soil). A major finding was that low doses and dose rates of gamma rays can significantly suppress cancer induction by alpha radiation from inhaled Pu isotopes. The suppression relates to stimulation of the body's natural defenses, including immunity against cancer cells and selective apoptosis which removes precancerous and other aberrant cells.

  18. Structural Characterization of a Plutonium Sequestering Agent Complex by Synchrotron X-ray Diffraction

    SciTech Connect (OSTI)

    Gorden, A.E.V. |; Szigethy, G.; Tiedemann, B.E.F.; Xu, J.; Shuh, D.K.; Raymond, K.N. |

    2007-07-01

    New ligands and materials are required that can coordinate, sense, and purify actinides for selective extraction and reduction of toxic, radioactive wastes from the mining and purification of actinides. The similarities in the chemical, biological transport, and distribution properties of Fe(III) and Pu(IV) inspired a bio-mimetic approach to the development of sequestering agents for actinides. A detailed evaluation of the structure and bonding of actinide coordinating ligands like these is important for the design of new selective ligand systems. Knowing the difficulty with working with the crystals resulting from these ligand systems and safe handling considerations for working with Pu, procedures were developed that utilize the Advanced Light Source of Lawrence Berkeley National Laboratory to determine the solid-state structures of Pu complexes by X-ray diffraction. (au0011tho.

  19. Reaction kinetics relevant to the recycle hydride-dehydride process for plutonium recovery

    SciTech Connect (OSTI)

    Haschke, J.M.; Allen, T.H.

    1997-10-01

    Objectives of this one-year, Laboratory Directed Research and Development (LDRD) project were the expansion of fundamental knowledge of plutonium chemistry and the development of information for enhancing plutonium recovery methods and weapons safety. Results of kinetic studies demonstrate that the monoxide monohydride, PuO(H), formed during corrosion of plutonium by water in pyrophoric when dry and acts as an initiator for hydride-catalyzed reaction of the metal with air. The catalyzed corrosion rate of Pu is 10{sup 8} times faster than that in dry air and transforms plutonium into a readily aerosolized material. A potential application for the catalytic reaction is in the direct recovery of plutonium as oxide. Wet PuO(H) is non-pyrophoric and the safety hazard posed by its formation is reduced if the material is not allowed to dry.

  20. A Note on the Reaction of Hydrogen and Plutonium

    SciTech Connect (OSTI)

    Noone, Bailey C

    2012-08-15

    Plutonium hydride has many practical and experimental purposes. The reaction of plutonium and hydrogen has interesting characteristics, which will be explored in the following analysis. Plutonium is a radioactive actinide metal that emits alpha particles. When plutonium metal is exposed to air, the plutonium oxides and hydrides, and the volume increases. PuH{sub 2} and Pu{sub 2}O{sub 3} are the products. Hydrogen is a catalyst for plutonium's corrosion in air. The reaction can take place at room temperature because it is fairly insensitive to temperature. Plutonium hydride, or PuH{sub 2}, is black and metallic. After PuH{sub 2} is formed, it quickly flakes off and burns. The reaction of hydrogen and plutonium is described as pyrophoric because the product will spontaneously ignite when oxygen is present. This tendency must be considered in the storage of metal plutonium. The reaction is characterized as reversible and nonstoichiometric. The reaction goes as such: Pu + H{sub 2} {yields} PuH{sub 2}. When PuH{sub 2} is formed, the hydrogen/plutonium ratio is between 2 and 2.75 (approximately). As more hydrogen is added to the system, the ratio increases. When the ratio exceeds 2.75, PuH{sub 3} begins to form along with PuH{sub 2}. Once the ratio surpasses 2.9, only PuH{sub 3} remains. The volume of the plutonium sample increases because of the added hydrogen and the change in crystal structure which the sample undergoes. As more hydrogen is added to a system of metal plutonium, the crystal structure evolves. Plutonium has a crystal structure classified as monoclinic. A monoclinic crystal structure appears to be a rectangular prism. When plutonium reacts with hydrogen, the product PuH{sub 2}, becomes a fluorite structure. It can also be described as a face centered cubic structure. PuH{sub 3} forms a hexagonal crystal structure. As plutonium evolves from metal plutonium to plutonium hydride to plutonium trihydride, the crystal structure evolves from monoclinic to fluorite to hexagonal. This change in crystal structure as a result of adding hydrogen is a shared characteristic with other actinide elements. Americium is isostructural with plutonium because they both form cubic dihyrides and hexagonal trihydrides. Reacting hydrogen with plutonium has the practical application of separating plutonium from other materials that don't react as well with hydrogen. When plutonium is placed in a chamber where there is very little oxygen, it can react with hydrogen without igniting. The hydrogen plutonium reaction can then be reversed, thus regaining the separated plutonium. Another application of this reaction is that it can be used to predict how plutonium reacts with other substances. Deuterium and tritium are two isotopes of hydrogen that are of interest. They are known to react likewise to hydrogen because they have similar properties. The reaction of plutonium and isotopes of hydrogen can prove to be very informative.

  1. Subthreshold Photofission of Even-Even Nuclei

    SciTech Connect (OSTI)

    Kadmensky, S.G.; Rodionova, L.V. [Voronezh State University, Universitetskaya pl. 1, Voronezh, 394693 (Russian Federation)

    2005-09-01

    Within quantum-mechanical fission theory, the angular distributions of fragments originating from the subthreshold photofission of the even-even nuclei {sup 232}Th, {sup 234}U, {sup 236}U, {sup 238}U, {sup 238}Pu, {sup 240}Pu, and {sup 242}Pu are analyzed for photon energies below 7 MeV. Special features of various fission channels are assessed under the assumption that the fission barrier has a two-humped shape. It is shown that the maximum value of the relative orbital angular momentum L{sub m} of fission fragments can be found upon taking into account deviations from the predictions of A. Bohr's formula for the angular distributions of fission fragments. The result is L{sub m} {approx_equal} 30. The existence of an 'isomeric shelf' for the angular distributions of fragments from {sup 236}U and {sup 238}U photofission in the low-energy region is confirmed.

  2. FEASIBILITY OF RECYCLING PLUTONIUM AND MINOR ACTINIDES IN LIGHT WATER REACTORS USING HYDRIDE FUEL

    SciTech Connect (OSTI)

    Greenspan, Ehud; Todreas, Neil; Taiwo, Temitope

    2009-03-10

    The objective of this DOE NERI program sponsored project was to assess the feasibility of improving the plutonium (Pu) and minor actinide (MA) recycling capabilities of pressurized water reactors (PWRs) by using hydride instead of oxide fuels. There are four general parts to this assessment: 1) Identifying promising hydride fuel assembly designs for recycling Pu and MAs in PWRs 2) Performing a comprehensive systems analysis that compares the fuel cycle characteristics of Pu and MA recycling in PWRs using the promising hydride fuel assembly designs identified in Part 1 versus using oxide fuel assembly designs 3) Conducting a safety analysis to assess the likelihood of licensing hydride fuel assembly designs 4) Assessing the compatibility of hydride fuel with cladding materials and water under typical PWR operating conditions Hydride fuel was found to offer promising transmutation characteristics and is recommended for further examination as a possible preferred option for recycling plutonium in PWRs.

  3. Study on the properties of saline HLLW in China

    SciTech Connect (OSTI)

    Liang, J.F.; Liu, X.G.; Song, C.L.; Jiao, R.Z.

    2008-07-01

    The properties and the components of HLLW (High-level Liquid Waste) were studied. The genuine saline HLLW is a blue-green liquid with 1.399 g/mL density. The activities of {sup 137}Cs, {sup 90}Sr, {sup 99}Tc, {sup 237}Np, {sup 239}Pu, {sup 241}Am, and total {alpha}/{beta}/{gamma} were determined. The extractive properties of actinide s in the HLLW were examined in a five-stage cross-extraction test. More than 98% of the Pu in HLLW is Pu{sup 4+}, and more than 70% of the Np is Np{sup 4+}. It was shown that >99.97% of the {alpha}-nuclides were extracted by 30% TRPO-kerosene from the HLLW. The separation performance of actinides is excellent. (authors)

  4. Ground state properties and high pressure behavior of plutonium dioxide: Systematic density functional calculations

    E-Print Network [OSTI]

    Zhang, Ping; Zhao, Xian-Geng

    2010-01-01

    Plutonium dioxide is of high technological importance in nuclear fuel cycle and is particularly crucial in long-term storage of Pu-based radioactive waste. Using first-principles density-functional theory, in this paper we systematically study the structural, electronic, mechanical, thermodynamic properties, and pressure induced structural transition of PuO$_{2}$. To properly describe the strong correlation in the Pu $5f$ electrons, the local density approximation$+U$ and the generalized gradient approximation$+U$ theoretical formalisms have been employed. We optimize the $U$ parameter in calculating the total energy, lattice parameters, and bulk modulus at the nonmagnetic, ferromagnetic, and antiferromagnetic configurations for both ground state fluorite structure and high pressure cotunnite structure. The best agreement with experiments is obtained by tuning the effective Hubbard parameter $U$ at around 4 eV within the LDA$+U$ approach. After carefully testing the validity of the ground state, we further in...

  5. Development of an improved sodium titanate for the pretreatment of nuclear waste at the Savannah River Site

    SciTech Connect (OSTI)

    Hobbs, D.T.; Poirier, M.R.; Barnes, M.J.; Peters, T.B.; Fondeur, F.F.; Thompson, M.E.; Fink, S.D. [Savannah River National Laboratory, Westinghouse Savannah River Company, Aiken, SC (United States); Nyman, M.D. [Sandia National Laboratories, Albuquerque, NM (United States)

    2008-07-01

    High-level nuclear waste produced from fuel reprocessing operations at the Savannah River Site (SRS) requires pretreatment to remove Cs-137, Sr-90 and alpha-emitting radionuclides (i.e., actinides) prior to disposal onsite as low level waste. Separation processes planned at SRS include sorption of Sr-90 and alpha-emitting radionuclides onto monosodium titanate (MST) and caustic side solvent extraction, for Cs-137 removal. The MST and separated Cs-137 will be encapsulated into a borosilicate glass wasteform for eventual entombment at the federal repository. The predominant alpha-emitting radionuclides in the highly alkaline waste solutions include plutonium isotopes Pu-238, Pu-239 and Pu-240. This paper describes recent results to produce an improved sodium titanate material that exhibits increased removal kinetics and capacity for Sr-90 and alpha-emitting radionuclides compared to the baseline MST material. (authors)

  6. Recommended Method To Account For Daughter Ingrowth For The Portsmouth On-Site Waste Disposal Facility Performance Assessment Modeling

    SciTech Connect (OSTI)

    Phifer, Mark A.; Smith, Frank G. III

    2013-06-21

    A 3-D STOMP model has been developed for the Portsmouth On-Site Waste Disposal Facility (OSWDF) at Site D as outlined in Appendix K of FBP 2013. This model projects the flow and transport of the following radionuclides to various points of assessments: Tc-99, U-234, U-235, U-236, U-238, Am-241, Np-237, Pu-238, Pu-239, Pu-240, Th-228, and Th-230. The model includes the radioactive decay of these parents, but does not include the associated daughter ingrowth because the STOMP model does not have the capability to model daughter ingrowth. The Savannah River National Laboratory (SRNL) provides herein a recommended method to account for daughter ingrowth in association with the Portsmouth OSWDF Performance Assessment (PA) modeling.

  7. Investigation of the Performance of D2O-Cooled High-Conversion Reactors for Fuel Cycle Calculations

    SciTech Connect (OSTI)

    Hikaru Hiruta; Gilles Youinou

    2013-09-01

    This report presents FY13 activities for the analysis of D2O cooled tight-pitch High-Conversion PWRs (HCPWRs) with U-Pu and Th-U fueled cores aiming at break-even or near breeder conditions while retaining the negative void reactivity. The analyses are carried out from several aspects which could not be covered in FY12 activities. SCALE 6.1 code system is utilized, and a series of simple 3D fuel pin-cell models are developed in order to perform Monte Carlo based criticality and burnup calculations. The performance of U-Pu fueled cores with axial and internal blankets is analyzed in terms of their impact on the relative fissile Pu mass balance, initial Pu enrichment, and void coefficient. In FY12, Pu conversion performances of D2O-cooled HCPWRs fueled with MOX were evaluated with small sized axial/internal DU blankets (approximately 4cm of axial length) in order to ensure the negative void reactivity, which evidently limits the conversion performance of HCPWRs. In this fiscal year report, the axial sizes of DU blankets are extended up to 30 cm in order to evaluate the amount of DU necessary to reach break-even and/or breeding conditions. Several attempts are made in order to attain the milestone of the HCPWR designs (i.e., break-even condition and negative void reactivity) by modeling of HCPWRs under different conditions such as boiling of D2O coolant, MOX with different 235U enrichment, and different target burnups. A similar set of analyses are performed for Th-U fueled cores. Several promising characteristics of 233U over other fissile like 239Pu and 235U, most notably its higher fission neutrons per absorption in thermal and epithermal ranges combined with lower ___ in the fast range than 239Pu allows Th-U cores to be taller than MOX ones. Such an advantage results in 4% higher relative fissile mass balance than that of U-Pu fueled cores while retaining the negative void reactivity until the target burnup of 51 GWd/t. Several other distinctions between U-Pu and Th-U fueled cores are identified by evaluating the sensitivity coefficients of keff, mass balance, and void coefficient. The effect of advanced iron alloy cladding (i.e., FeCrAl) on the performance of Pu conversion in MOX fueled cores is studied instead of using standard stainless-steel cladding. Variations in clad thickness and coolant-to-fuel volume ratio are also exercised. The use of FeCrAl instead of SS as a cladding alloy reduces the required Pu enrichment and improves the Pu conversion rate primarily due to the absence of nickel in the cladding alloy that results in the reduction of the neutron absorption. Also the difference in void coefficients between SS and FeCrAl alloys is nearly 500 pcm over the entire burnup range. The report also shows sensitivity and uncertainty analyses in order to characterize D2O cooled HCPWRs from different aspects. The uncertainties of integral parameters (keff and void coefficient) for selected reactor cores are evaluated at different burnup points in order to find similarities and trends respect to D2O-HCPWR.

  8. Influence of soil biopopulation on migration of waste radionuclides

    SciTech Connect (OSTI)

    Fowler, E.B.; Polzer, W.L.; Essington, E.H.

    1983-01-01

    This paper reports the interpretation of some results obtained when a Maxey Flats burial pit radioactive waste solution was reacted with a Tilsit soil. The influence of a biopopulation on the degree of sorption and on the stability of that system was investigated. The data have been interpreted as follows: the removal of /sup 137/Cs from solution by the soil is essentially complete within a one-hour period and is not influenced by an active biopopulation. The soil studied contains complexers which solublize /sup 238/Pu. The soluble complex does not sorb to soil and thus is potentially mobile. In the presence of an active biopopulation 86% of the complexes is degraded; the released /sup 238/Pu was rendered immobile. The remaining 14% of the soluble /sup 238/Pu was not released to the soil during 53 days incubation. That fraction is heat stable and non- or slowly-biodegradable and thus retains its potential to migrate.

  9. Plutonium (III) and uranium (III) nitrile complexes

    SciTech Connect (OSTI)

    Enriquez, A. E.; Matonic, J. H.; Scott, B. L.; Neu, M. P.

    2002-01-01

    Iodine oxidation of uranium and plutonium metals in tetrahydrofuran and pyridine form AnI{sub 3}(THF){sub 4} and AnI{sub 3}(py){sub 4} (An = Pu, U). These compounds represent convenient entries Into solution An(III) chemistry in organic solvents. Extensions of the actinide metal oxidation methodology in nitrile solvents by I{sub 2}, AgPF{sub 6}, and TIPF{sub 6} are presented here. Treatment of Pu{sup 0} in acetonitrile with iodine yields a putative PuI{sub 3}(NCMe){sub x} intermediate which can be trapped with the tripodal nitrogen donor ligand tpza (tpza = (tris[(2-pyrazinyl)methyl]amine)) and forms the eight-coordinate complex (tpza)PuI{sub 3}(NCMe). Treatment of excess U{sup 0} metal by iodine in acetonitrile afforded a brown crystalline mixed valence complex, [U(NCMe){sub 9}][UI{sub 6}][I], instead of UI{sub 3}(NCMe){sub 4}. The analogous reaction in bezonitrile forms red crystalline UI{sub 4}(NCPh){sub 4}. In contrast, treatment of UI{sub 3}(THF){sub 4} with excess acetonitrile cleanly generates [U(NCMe){sub 9}][I]{sub 3}. Oxidation of Pu{sup 0} by either TI(I) or Ag(I) hexafluorophosphate salts generates a nine-coordinate homoleptic acetonitrile adduct [Pu(NCMe){sub 9}][PF{sub 6}]{sub 3}. Attempts to oxidize U{sub 0} with these salts were unsuccessful.

  10. ARRAYS OF BOTTLES OF PLUTONIUM NITRATE SOLUTION

    SciTech Connect (OSTI)

    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.

  11. Evaluation of Impurity Extremes in a Plutonium-loaded Borosilicate Glass

    SciTech Connect (OSTI)

    Fox, K.M.; Crawford, C.L.; Marra, J.C.; Bibler, N.E.; Hoffman, E.N.; Edwards, T.B. [Savannah River National Laboratory, Aiken, SC (United States)

    2008-07-01

    A vitrification technology utilizing a lanthanide borosilicate (LaBS) glass appears to be a viable option for the disposition of excess weapons-usable plutonium that is not suitable for processing into mixed oxide (MOX) fuel. A significant effort to develop a glass formulation and vitrification process to immobilize plutonium was completed in the mid-1990's. The LaBS glass formulation was found to be capable of immobilizing in excess of 10 wt % Pu and to be tolerant of a range of impurities. To confirm the results of previous testing with surrogate Pu feeds containing impurities, four glass compositions were selected for fabrication with actual plutonium oxide and impurities. The four compositions represented extremes in impurity type and concentration. The homogeneity and durability of these four compositions were measured. The homogeneity of the glasses was evaluated using x-ray diffraction (XRD) and scanning electron microscopy coupled with energy dispersive spectroscopy (SEM/EDS). The XRD results indicated that the glasses were amorphous with no evidence of crystalline species in the glass. The SEM/EDS analyses did show the presence of some undissolved PuO{sub 2} material. The EDS spectra indicated that some of the PuO{sub 2} crystals also contained hafnium oxide. The SEM/EDS analyses showed that there were no heterogeneities in the glass due to the feed impurities. The durability of the glasses was measured using the Product Consistency Test (PCT). The PCT results indicated that the durability of Pu impurity glasses was comparable with Pu glasses without impurities and significantly more durable than the Environmental Assessment (EA) glass used as the benchmark for repository disposition of high-level waste (HLW) glasses. (authors)

  12. EVALUATION OF IMPURITY EXTREMES IN A PLUTONIUM-LOADED BOROSILICATE GLASS

    SciTech Connect (OSTI)

    Marra, J; Kevin Fox, K; Charles Crawford, C; Ned Bibler, N; Elizabeth Hoffman, E; Tommy Edwards, T

    2007-11-12

    A vitrification technology utilizing a lanthanide borosilicate (LaBS) glass appears to be a viable option for the disposition of excess weapons-useable plutonium that is not suitable for processing into mixed oxide (MOX) fuel. A significant effort to develop a glass formulation and vitrification process to immobilize plutonium was completed in the mid-1990s. The LaBS glass formulation was found to be capable of immobilizing in excess of 10 wt % Pu and to be tolerant of a range of impurities. To confirm the results of previous testing with surrogate Pu feeds containing impurities, four glass compositions were selected for fabrication with actual plutonium oxide and impurities. The four compositions represented extremes in impurity type and concentration. The homogeneity and durability of these four compositions were measured. The homogeneity of the glasses was evaluated using x-ray diffraction (XRD) and scanning electron microscopy coupled with energy dispersive spectroscopy (SEM/EDS). The XRD results indicated that the glasses were amorphous with no evidence of crystalline species in the glass. The SEM/EDS analyses did show the presence of some undissolved PuO{sub 2} material. The EDS spectra indicated that some of the PuO{sub 2} crystals also contained hafnium oxide. The SEM/EDS analyses showed that there were no heterogeneities in the glass due to the feed impurities. The durability of the glasses was measured using the Product Consistency Test (PCT). The PCT results indicated that the durability of Pu impurity glasses was comparable with Pu glasses without impurities and significantly more durable than the Environmental Assessment (EA) glass used as the benchmark for repository disposition of high-level waste (HLW) glasses.

  13. Radionuclides and heavy metals in rainbow trout from Tsichomo, Nana Ka, Wen Povi, and Pin De Lakes in Santa Clara Canyon

    SciTech Connect (OSTI)

    Fresquez, P.R.; Armstrong, D.R.; Naranjo, L. Jr.

    1998-04-01

    Radionuclide ({sup 3}H, {sup 90}Sr, {sup 137}Cs, {sup 238}Pu, {sup 239}Pu, and total uranium) and heavy metal (Ag, As, Ba, Be, Cd, Cr, Hg, Ni, Pb, Sb, Se, and TI) concentrations were determined in rainbow trout collected from Tsichomo, Nana Ka, Wen Povi, and Pin De lakes in Santa Clara Canyon in 1997. Most radionuclide and heavy metal concentrations in fish collected from these four lakes were within or just above upper limit background concentrations (Abiquiu reservoir), and as a group were statistically (p < 0.05) similar in most parameters to background.

  14. Special education in Costa Rica 

    E-Print Network [OSTI]

    Stough, Laura

    2014-01-01

    Universidad Estatal a Distancia. Mele´ndez, L. (2000). Aspectos histo´ricos de la atencio´n a las personas con necesidades educativas especiales en Costa Rica y el mundo [Historical aspects of the attention of persons with special education needs in Costa Rica... Educacio´n Pu´blica. (2010). Bolet?´n 11-10: Necesi- dades educativas especiales en centros que brindan educacio´n tradicional [Special education needs in traditional education centers]. Costa Rica: MEP. Ministerio de Educacio´n Pu´blica. (2011). Matr?...

  15. Conceptual Design for the Pilot-Scale Plutonium Oxide Processing Unit in the Radiochemical Processing Laboratory

    SciTech Connect (OSTI)

    Lumetta, Gregg J.; Meier, David E.; Tingey, Joel M.; Casella, Amanda J.; Delegard, Calvin H.; Edwards, Matthew K.; Jones, Susan A.; Rapko, Brian M.

    2014-08-05

    This report describes a conceptual design for a pilot-scale capability to produce plutonium oxide for use as exercise and reference materials, and for use in identifying and validating nuclear forensics signatures associated with plutonium production. This capability is referred to as the Pilot-scale Plutonium oxide Processing Unit (P3U), and it will be located in the Radiochemical Processing Laboratory at the Pacific Northwest National Laboratory. The key unit operations are described, including plutonium dioxide (PuO2) dissolution, purification of the Pu by ion exchange, precipitation, and conversion to oxide by calcination.

  16. Spectral analysis of slender tensioned cylinder interaction 

    E-Print Network [OSTI]

    Diao, Weiguo

    1998-01-01

    the coefficient k, and c, are constants: Case I The Duffing nonlinear system is defined by p(u, u, t) =k, u'(t) Case 2 The Van der Pol nonlinear system is defined by (60) p(u, u, t)= ? ? u (t)= c, u (t)u(t) c, c 3 Ct (6l) Case 3 The combined Duffing-Van der... models, the Duffing model, the Van Der Pol model and a combination model will be examined using the test data obtained in the study by Rijken (1997). By developing a better understanding of the interactive behavior between two tensioned tandem...

  17. Neptunium storage at Hanford

    SciTech Connect (OSTI)

    Alderman, C.J.; Shiraga, S.S.; Schwartz, R.A.; Smith, R.J.; Wootan, D.W.

    1993-06-01

    A decision must be made regarding whether the United State`s stockpile of neptunium should be discarded into the waste stream or kept for the production of Pu-238. Although the cost of long term storage is not inconsequential, to dispose of the material means the closing of our option to maintain control over our Pu-238 stockpile. Within the Fuels and Materials Examination Facility at Hanford there exists a remotely operated facility that can be converted for neptunium storage. This paper describes the facility and the anticipated handling requirements.

  18. Separation and Purification and Beta Liquid Scintillation Analysis of Sm-151 in Savannah River Site and Hanford Site DOE High Level Waste

    SciTech Connect (OSTI)

    Dewberry, R.A.

    2001-02-13

    This paper describes development work to obtain a product phase of Sm-151 pure of any other radioactive species so that it can be determined in US Department of Energy high level liquid waste and low level solid waste by liquid scintillation {beta}-spectroscopy. The technique provides separation from {mu}Ci/ml levels of Cs-137, Pu alpha and Pu-241 {beta}-decay activity, and Sr-90/Y-90 activity. The separation technique is also demonstrated to be useful for the determination of Pm-147.

  19. Sustained Recycle in Light Water and Sodium-Cooled Reactors

    SciTech Connect (OSTI)

    Steven J. Piet; Samuel E. Bays; Michael A. Pope; Gilles J. Youinou

    2010-11-01

    From a physics standpoint, it is feasible to sustain recycle of used fuel in either thermal or fast reactors. This paper examines multi-recycle potential performance by considering three recycling approaches and calculating several fuel cycle parameters, including heat, gamma, and neutron emission of fresh fuel; radiotoxicity of waste; and uranium utilization. The first recycle approach is homogeneous mixed oxide (MOX) fuel assemblies in a light water reactor (LWR). The transuranic portion of the MOX was varied among Pu, NpPu, NpPuAm, or all-TRU. (All-TRU means all isotopes through Cf-252.) The Pu case was allowed to go to 10% Pu in fresh fuel, but when the minor actinides were included, the transuranic enrichment was kept below 8% to satisfy the expected void reactivity constraint. The uranium portion of the MOX was enriched uranium. That enrichment was increased (to as much as 6.5%) to keep the fuel critical for a typical LWR irradiation. The second approach uses heterogeneous inert matrix fuel (IMF) assemblies in an LWR - a mix of IMF and traditional UOX pins. The uranium-free IMF fuel pins were Pu, NpPu, NpPuAm, or all-TRU. The UOX pins were limited to 4.95% U-235 enrichment. The number of IMF pins was set so that the amount of TRU in discharged fuel from recycle N (from both IMF and UOX pins) was made into the new IMF pins for recycle N+1. Up to 60 of the 264 pins in a fuel assembly were IMF. The assembly-average TRU content was 1-6%. The third approach uses fast reactor oxide fuel in a sodium-cooled fast reactor with transuranic conversion ratio of 0.50 and 1.00. The transuranic conversion ratio is the production of transuranics divided by destruction of transuranics. The FR at CR=0.50 is similar to the CR for the MOX case. The fast reactor cases had a transuranic content of 33-38%, higher than IMF or MOX.

  20. Lead Slowing-Down Spectrometry Time Spectral Analysis for Spent Fuel Assay: FY11 Status Report

    SciTech Connect (OSTI)

    Kulisek, Jonathan A.; Anderson, Kevin K.; Bowyer, Sonya M.; Casella, Andrew M.; Gesh, Christopher J.; Warren, Glen A.

    2011-09-30

    Developing a method for the accurate, direct, and independent assay of the fissile isotopes in bulk materials (such as used fuel) from next-generation domestic nuclear fuel cycles is a goal of the Office of Nuclear Energy, Fuel Cycle R&D, Material Protection and Control Technology (MPACT) Campaign. To meet this goal, MPACT supports a multi-institutional collaboration, of which PNNL is a part, to study the feasibility of Lead Slowing Down Spectroscopy (LSDS). This technique is an active nondestructive assay method that has the potential to provide independent, direct measurement of Pu and U isotopic masses in used fuel with an uncertainty considerably lower than the approximately 10% typical of today's confirmatory assay methods. This document is a progress report for FY2011 PNNL analysis and algorithm development. Progress made by PNNL in FY2011 continues to indicate the promise of LSDS analysis and algorithms applied to used fuel. PNNL developed an empirical model based on calibration of the LSDS to responses generated from well-characterized used fuel. The empirical model, which accounts for self-shielding effects using empirical basis vectors calculated from the singular value decomposition (SVD) of a matrix containing the true self-shielding functions of the used fuel assembly models. The potential for the direct and independent assay of the sum of the masses of 239Pu and 241Pu to within approximately 3% over a wide used fuel parameter space was demonstrated. Also, in FY2011, PNNL continued to develop an analytical model. Such efforts included the addition of six more non-fissile absorbers in the analytical shielding function and the non-uniformity of the neutron flux across the LSDS assay chamber. A hybrid analytical-empirical approach was developed to determine the mass of total Pu (sum of the masses of 239Pu, 240Pu, and 241Pu), which is an important quantity in safeguards. Results using this hybrid method were of approximately the same accuracy as the pure empirical approach. In addition, total Pu with much better accuracy with the hybrid approach than the pure analytical approach. In FY2012, PNNL will continue efforts to optimize its empirical model and minimize its reliance on calibration data. In addition, PNNL will continue to develop an analytical model, considering effects such as neutron-scattering in the fuel and cladding, as well as neutrons streaming through gaps between fuel pins in the fuel assembly.