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Sample records for atmosphere fission product

  1. Fission Product Library and Resource

    SciTech Connect

    Burke, J. T.; Padgett, S.

    2016-09-29

    Fission product yields can be extracted from an irradiated sample by performing gamma ray spectroscopy on the whole sample post irradiation. There are several pitfalls to avoid when trying to determine a specific isotope's fission product yield.

  2. TREATMENT OF FISSION PRODUCT WASTE

    DOEpatents

    Huff, J.B.

    1959-07-28

    A pyrogenic method of separating nuclear reactor waste solutions containing aluminum and fission products as buring petroleum coke in an underground retort, collecting the easily volatile gases resulting as the first fraction, he uminum chloride as the second fraction, permitting the coke bed to cool and ll contain all the longest lived radioactive fission products in greatly reduced volume.

  3. PRODUCING ENERGY AND RADIOACTIVE FISSION PRODUCTS

    DOEpatents

    Segre, E.; Kennedy, J.W.; Seaborg, G.T.

    1959-10-13

    This patent broadly discloses the production of plutonium by the neutron bombardment of uranium to produce neptunium which decays to plutonium, and the fissionability of plutonium by neutrons, both fast and thermal, to produce energy and fission products.

  4. The SPIDER fission fragment spectrometer for fission product yield measurements

    SciTech Connect

    Meierbachtol, K.; Tovesson, F.; Shields, D.; Arnold, C.; Blakeley, R.; Bredeweg, T.; Devlin, M.; Hecht, A. A.; Heffern, L. E.; Jorgenson, J.; Laptev, A.; Mader, D.; O׳Donnell, J. M.; Sierk, A.; White, M.

    2015-04-01

    We developed the SPectrometer for Ion DEtermination in fission Research (SPIDER) for measuring mass yield distributions of fission products from spontaneous and neutron-induced fission. The 2E–2v method of measuring the kinetic energy (E) and velocity (v) of both outgoing fission products has been utilized, with the goal of measuring the mass of the fission products with an average resolution of 1 atomic mass unit (amu). Moreover, the SPIDER instrument, consisting of detector components for time-of-flight, trajectory, and energy measurements, has been assembled and tested using 229Th and 252Cf radioactive decay sources. For commissioning, the fully assembled system measured fission products from spontaneous fission of 252Cf. Individual measurement resolutions were met for time-of-flight (250 ps FWHM), spacial resolution (2 mm FHWM), and energy (92 keV FWHM for 8.376 MeV). Finally, these mass yield results measured from 252Cf spontaneous fission products are reported from an E–v measurement.

  5. The SPIDER fission fragment spectrometer for fission product yield measurements

    DOE PAGES

    Meierbachtol, K.; Tovesson, F.; Shields, D.; ...

    2015-04-01

    We developed the SPectrometer for Ion DEtermination in fission Research (SPIDER) for measuring mass yield distributions of fission products from spontaneous and neutron-induced fission. The 2E–2v method of measuring the kinetic energy (E) and velocity (v) of both outgoing fission products has been utilized, with the goal of measuring the mass of the fission products with an average resolution of 1 atomic mass unit (amu). Moreover, the SPIDER instrument, consisting of detector components for time-of-flight, trajectory, and energy measurements, has been assembled and tested using 229Th and 252Cf radioactive decay sources. For commissioning, the fully assembled system measured fission productsmore » from spontaneous fission of 252Cf. Individual measurement resolutions were met for time-of-flight (250 ps FWHM), spacial resolution (2 mm FHWM), and energy (92 keV FWHM for 8.376 MeV). Finally, these mass yield results measured from 252Cf spontaneous fission products are reported from an E–v measurement.« less

  6. Measurement of Fission Product Yields from Fast-Neutron Fission

    NASA Astrophysics Data System (ADS)

    Arnold, C. W.; Bond, E. M.; Bredeweg, T. A.; Fowler, M. M.; Moody, W. A.; Rusev, G.; Vieira, D. J.; Wilhelmy, J. B.; Becker, J. A.; Henderson, R.; Kenneally, J.; Macri, R.; McNabb, D.; Ryan, C.; Sheets, S.; Stoyer, M. A.; Tonchev, A. P.; Bhatia, C.; Bhike, M.; Fallin, B.; Gooden, M. E.; Howell, C. R.; Kelley, J. H.; Tornow, W.

    2014-09-01

    One of the aims of the Stockpile Stewardship Program is a reduction of the uncertainties on fission data used for analyzing nuclear test data [1,2]. Fission products such as 147Nd are convenient for determining fission yields because of their relatively high yield per fission (about 2%) and long half-life (10.98 days). A scientific program for measuring fission product yields from 235U,238U and 239Pu targets as a function of bombarding neutron energy (0.1 to 15 MeV) is currently underway using monoenergetic neutron beams produced at the 10 MV Tandem Accelerator at TUNL. Dual-fission chambers are used to determine the rate of fission in targets during activation. Activated targets are counted in highly shielded HPGe detectors over a period of several weeks to identify decaying fission products. To date, data have been collected at neutron bombarding energies 4.6, 9.0, 14.5 and 14.8 MeV. Experimental methods and data reduction techniques are discussed, and some preliminary results are presented.

  7. The phebus fission product project

    NASA Astrophysics Data System (ADS)

    von der Hardt, P.; Tattegrain, A.

    1992-06-01

    A new facility is being built at the Phebus test reactor in Cadarache, France, for investigations into phenomena of fuel damage and fission product (FP) release under severe power reactor accident conditions, as part of a large international research program. Phebus FP simulates core, cooling system and containment of an accidented reactor by appropriate scaled-down experimental components. The test fuel, with 25 to 30 GWd/t burnup, is re-irradiated in situ and then overheated up to UO 2 melting. Fission products and other aerosols are swept through the primary pipework into the containment vessel, by hot steam and hydrogen. Experimental instrumentation and posttest analyses will enable the following main phenomena to be studied: structural material and fuel dislocation, final fuel state; release, chemical form and transport/depletion of fission products in the facility, particularly aerosol physics, including nonfission product material and iodine chemistry in terms of volatile species formation through radiolysis, reactions with organic material, aerosol-vapor reactions, etc. Design and development of equipment and experimental procedures are supported by modeling and code calculations with the scope of predicting the experimental sequence, on one hand, and to prepare code validation through the results, on the other hand. More than 25 organisation from Europe and overseas, collaborate in the scientific and technological development of the Phebus FP program. The first in-pile test is planned for spring 1993, and five subsequent experiments are scheduled to follow in yearly intervals. This paper describes facility and support activities, and highlights a number of nuclear materials aspects involved.

  8. RECOVERY OF ALUMINUM FROM FISSION PRODUCTS

    DOEpatents

    Blanco, R.E.; Higgins, I.R.

    1962-11-20

    A method is given for recovertng aluminum values from aqueous solutions containing said values together with fission products. A mixture of Fe/sub 2/O/ sub 3/ and MnO/sub 2/ is added to a solution containing aluminum and fission products. The resulting aluminum-containing supernatant is then separated from the fission product-bearing metal oxide precipitate and is contacted with a cation exchange resin. The aluminum sorbed on the resin is then eluted and recovered. (AEC)

  9. FISSION PRODUCT REMOVAL FROM ORGANIC SOLUTIONS

    DOEpatents

    Moore, R.H.

    1960-05-10

    The decontamination of organic solvents from fission products and in particular the treatment of solvents that were used for the extraction of uranium and/or plutonium from aqueous acid solutions of neutron-irradiated uranium are treated. The process broadly comprises heating manganese carbonate in air to a temperature of between 300 and 500 deg C whereby manganese dioxide is formed; mixing the manganese dioxide with the fission product-containing organic solvent to be treated whereby the fission products are precipitated on the manganese dioxide; and separating the fission product-containing manganese dioxide from the solvent.

  10. METHOD FOR SEPARATING PLUTONIUM AND FISSION PRODUCTS EMPLOYING AN OXIDE AS A CARRIER FOR FISSION PRODUCTS

    DOEpatents

    Davies, T.H.

    1961-07-18

    Carrier precipitation processes for separating plutonium values from uranium fission products are described. Silicon dioxide or titanium dioxide in a finely divided state is added to an acidic aqueous solution containing hexavalent plutonium ions together with ions of uranium fission products. The supernatant solution containing plutonium ions is then separated from the oxide and the fission products associated therewith.

  11. Fission-product retention in HTGR fuels

    SciTech Connect

    Homan, F.J.; Kania, M.J.; Tiegs, T.N.

    1982-01-01

    Retention data for gaseous and metallic fission products are presented for both Triso-coated and Biso-coated HTGR fuel particles. Performance trends are established that relate fission product retention to operating parameters, such as temperature, burnup, and neutron exposure. It is concluded that Biso-coated particles are not adequately retentive of fission gas or metallic cesium, and Triso-coated particles which retain cesium still lose silver. Design implications related to these performance trends are identified and discussed.

  12. ORNL fission product release tests VI-6

    SciTech Connect

    Osborne, M.F.; Lorenz, R.A.; Collins, J.L.; Lee, C.S.

    1991-01-01

    The ORNL fission product release tests investigate release and transport of the major fission products from high-burnup fuel under LWR accident conditions. The two most recent tests (VI-4 and VI-5) were conducted in hydrogen. In three previous tests in this series (VI-1, VI-2, and VI-3), which had been conducted in steam, the oxidized Zircaloy cladding remained largely intact and acted as a barrier to steam reaction with the UO{sub 2}. Test VI-6 was designed to insure significant oxidation of the UO{sub 2} fuel, which has been shown to enhance release of certain fission products, especially molybdenum and ruthenium. The BR3 fuel specimen used in test VI-6 will be heated in hydrogen to 2300 K; the Zircaloy cladding is expected to melt and runoff at {approximately}2150 K. Upon reaching the 2300 K test temperature, the test atmosphere will be changed to steam, and that temperature will be maintained for 60 min, with the three collection trains being operated for 2-, 18-, and 40-min periods. The releases of {sup 85}Kr and {sup 137}Cs will be monitored continuously throughout the test. Posttest analyses of the material collected on the three trains will provide results on the release and transport of Mo, Ru, Sb, Te, Ba, Ce, and Eu as a function of time at 2300 K. Continuous monitoring of the hydrogen produced during the steam atmosphere period at high temperature will provide a measure of the oxidation rate of the cladding and fuel. Following delays in approval of the safety documentation and in decontamination of the hot cell and test apparatus, test VI-6 will be conducted in late May.

  13. PROCESS FOR SEPARATING URANIUM FISSION PRODUCTS

    DOEpatents

    Spedding, F.H.; Butler, T.A.; Johns, I.B.

    1959-03-10

    The removal of fission products such as strontium, barium, cesium, rubidium, or iodine from neutronirradiated uranium is described. Uranium halide or elemental halogen is added to melted irradiated uranium to convert the fission products to either more volatile compositions which vaporize from the melt or to higher melting point compositions which separate as solids.

  14. Fission products in National Atmospheric Deposition Program—Wet deposition samples prior to and following the Fukushima Dai-Ichi Nuclear Power Plant incident, March 8?April 5, 2011

    USGS Publications Warehouse

    Wetherbee, Gregory A.; Debey, Timothy M.; Nilles, Mark A.; Lehmann, Christopher M.B.; Gay, David A.

    2012-01-01

    Radioactive isotopes I-131, Cs-134, or Cs-137, products of uranium fission, were measured at approximately 20 percent of 167 sampled National Atmospheric Deposition Program monitoring sites in North America (primarily in the contiguous United States and Alaska) after the Fukushima Dai-Ichi Nuclear Power Plant incident on March 12, 2011. Samples from the National Atmospheric Deposition Program were analyzed for the period of March 8-April 5, 2011. Calculated 1- or 2-week radionuclide deposition fluxes at 35 sites from Alaska to Vermont ranged from 0.47 to 5,100 Becquerels per square meter during the sampling period of March 15-April 5, 2011. No fission-product isotopes were measured in National Atmospheric Deposition Program samples obtained during March 8-15, 2011, prior to the arrival of contaminated air in North America.

  15. Downstream behavior of fission products

    SciTech Connect

    Johnson, I.; Farahat, M.K.; Settle, J.L.; Johnson, C.E.; Ritzman, R.

    1986-01-01

    The downstream behavior of fission products has been investigated by injecting mixtures of CsOH, CsI, and Te into a flowing steam/hydrogen stream and determining the physical and chemical changes that took place as the gaseous mixture flowed down a reaction duct on which a temperature gradient (1000/sup 0/ to 200/sup 0/C) had been imposed. Deposition on the wall of the duct occurred by vapor condensation in the higher temperature regions and by aerosol deposition in the remainder of the duct. Reactions in the gas stream between CsOH and CsI and between CsOH and Te had an effect on the vapor condensation. The aerosol was characterized by the use of impingement tabs placed in the gas stream.

  16. Computer program FPIP-REV calculates fission product inventory for U-235 fission

    NASA Technical Reports Server (NTRS)

    Brown, W. S.; Call, D. W.

    1967-01-01

    Computer program calculates fission product inventories and source strengths associated with the operation of U-235 fueled nuclear power reactor. It utilizes a fission-product nuclide library of 254 nuclides, and calculates the time dependent behavior of the fission product nuclides formed by fissioning of U-235.

  17. SOURCE OF PRODUCTS OF NUCLEAR FISSION

    DOEpatents

    Harteck, P.; Dondes, S.

    1960-03-15

    A source of fission product recoil energy suitable for use in radiation chemistry is reported. The source consists of thermal neutron irradiated glass wool having a diameter of 1 to 5 microns and containing an isotope fissionable by thermal neutrons, such as U/sup 235/.

  18. Thermodynamic analysis of volatile organometallic fission products.

    PubMed

    Auxier, John D; Jordan, Jacob A; Stratz, S Adam; Shahbazi, Shayan; Hanson, Daniel E; Cressy, Derek; Hall, Howard L

    The ability to perform rapid separations in a post nuclear weapon detonation scenario is an important aspect of national security. In the past, separations of fission products have been performed using solvent extraction, precipitation, etc. The focus of this work is to explore the feasibility of using thermochromatography, a technique largely employed in superheavy element chemistry, to expedite the separation of fission products from fuel components. A series of fission product complexes were synthesized and the thermodynamic parameters were measured using TGA/DSC methods. Once measured, these parameters were used to predict their retention times using thermochromatography.

  19. Transport properties of fission product vapors

    SciTech Connect

    Im, K.H.; Ahluwalia, R.K.

    1983-07-01

    Kinetic theory of gases is used to calculate the transport properties of fission product vapors in a steam and hydrogen environment. Provided in tabular form is diffusivity of steam and hydrogen, viscosity and thermal conductivity of the gaseous mixture, and diffusivity of cesium iodide, cesium hydroxide, diatomic tellurium and tellurium dioxide. These transport properties are required in determining the thermal-hydraulics of and fission product transport in light water reactors.

  20. Modeling Fission Product Sorption in Graphite Structures

    SciTech Connect

    Szlufarska, Izabela; Morgan, Dane; Allen, Todd

    2013-04-08

    The goal of this project is to determine changes in adsorption and desorption of fission products to/from nuclear-grade graphite in response to a changing chemical environment. First, the project team will employ principle calculations and thermodynamic analysis to predict stability of fission products on graphite in the presence of structural defects commonly observed in very high- temperature reactor (VHTR) graphites. Desorption rates will be determined as a function of partial pressure of oxygen and iodine, relative humidity, and temperature. They will then carry out experimental characterization to determine the statistical distribution of structural features. This structural information will yield distributions of binding sites to be used as an input for a sorption model. Sorption isotherms calculated under this project will contribute to understanding of the physical bases of the source terms that are used in higher-level codes that model fission product transport and retention in graphite. The project will include the following tasks: Perform structural characterization of the VHTR graphite to determine crystallographic phases, defect structures and their distribution, volume fraction of coke, and amount of sp2 versus sp3 bonding. This information will be used as guidance for ab initio modeling and as input for sorptivity models; Perform ab initio calculations of binding energies to determine stability of fission products on the different sorption sites present in nuclear graphite microstructures. The project will use density functional theory (DFT) methods to calculate binding energies in vacuum and in oxidizing environments. The team will also calculate stability of iodine complexes with fission products on graphite sorption sites; Model graphite sorption isotherms to quantify concentration of fission products in graphite. The binding energies will be combined with a Langmuir isotherm statistical model to predict the sorbed concentration of fission

  1. Recovery and use of fission product noble metals

    SciTech Connect

    Jensen, G.A.; Rohmann, C.A.; Perrigo, L.D.

    1980-06-01

    Noble metals in fission products are of strategic value. Market prices for noble metals are rising more rapidly than recovery costs. A promising concept has been developed for recovery of noble metals from fission product waste. Although the assessment was made only for the three noble metal fission products (Rh, Pd, Ru), there are other fission products and actinides which have potential value. (DLC)

  2. Electron spectra from decay of fission products

    SciTech Connect

    Dickens, J K

    1982-09-01

    Electron spectra following decay of individual fission products (72 less than or equal to A less than or equal to 162) are obtained from the nuclear data given in the compilation using a listed and documented computer subroutine. Data are given for more than 500 radionuclides created during or after fission. The data include transition energies, absolute intensities, and shape parameters when known. An average beta-ray energy is given for fission products lacking experimental information on transition energies and intensities. For fission products having partial or incomplete decay information, the available data are utilized to provide best estimates of otherwise unknown decay schemes. This compilation is completely referenced and includes data available in the reviewed literature up to January 1982.

  3. Fission Product Sorptivity in Graphite

    SciTech Connect

    Tompson, Jr., Robert V.; Loyalka, Sudarshan; Ghosh, Tushar; Viswanath, Dabir; Walton, Kyle; Haffner, Robert

    2015-04-01

    Both adsorption and absorption (sorption) of fission product (FP) gases on/into graphite are issues of interest in very high temperature reactors (VHTRs). In the original proposal, we proposed to use packed beds of graphite particles to measure sorption at a variety of temperatures and to use an electrodynamic balance (EDB) to measure sorption onto single graphite particles (a few μm in diameter) at room temperature. The use of packed beds at elevated temperature is not an issue. However, the TPOC requested revision of this initial proposal to included single particle measurements at elevated temperatures up to 1100 °C. To accommodate the desire of NEUP to extend the single particle EDB measurements to elevated temperatures it was necessary to significantly revise the plan and the budget. These revisions were approved. In the EDB method, we levitate a single graphite particle (the size, surface characteristics, morphology, purity, and composition of the particle can be varied) or agglomerate in the balance and measure the sorption of species by observing the changes in mass. This process involves the use of an electron stepping technique to measure the total charge on a particle which, in conjunction with the measured suspension voltages for the particle, allows for determinations of mass and, hence, of mass changes which then correspond to measurements of sorption. Accommodating elevated temperatures with this type of system required a significant system redesign and required additional time that ultimately was not available. These constraints also meant that the grant had to focus on fewer species as a result. Overall, the extension of the original proposed single particle work to elevated temperatures added greatly to the complexity of the proposed project and added greatly to the time that would eventually be required as well. This means that the bulk of the experimental progress was made using the packed bed sorption systems. Only being able to recruit one

  4. Average neutronic properties of prompt fission products

    SciTech Connect

    Foster, D.G. Jr.; Arthur, E.D.

    1982-02-01

    Calculations of the average neutronic properties of the ensemble of fission products producted by fast-neutron fission of /sup 235/U and /sup 239/Pu, where the properties are determined before the first beta decay of any of the fragments, are described. For each case we approximate the ensemble by a weighted average over 10 selected nuclides, whose properties we calculate using nuclear-model parameters deduced from the systematic properties of other isotopes of the same elements as the fission fragments. The calculations were performed primarily with the COMNUC and GNASH statistical-model codes. The results, available in ENDF/B format, include cross sections, angular distributions of neutrons, and spectra of neutrons and photons, for incident-neutron energies between 10/sup -5/ eV and 20 MeV. Over most of this energy range, we find that the capture cross section of /sup 239/Pu fission fragments is systematically a factor of two to five greater than for /sup 235/U fission fragments.

  5. Rapid separation of fresh fission products (draft)

    SciTech Connect

    Dry, D. E.; Bauer, E.; Petersen, L. A.

    2003-01-01

    The fission of highly eruiched uranium by thermal neutrons creates dozens of isotopic products. The Isotope and Nuclear Chemistry Group participates in programs that involve analysis of 'fiesh' fission products by beta counting following radiochemical separations. This is a laborious and time-consuming process that can take several days to generate results. Gamma spectroscopy can provide a more immediate path to isolopic activities, however short-lived, high-yield isotopes can swamp a gamma spectrum, making difficult the identification and quantification of isotopes on the wings and valley of the fission yield curve. The gamma spectrum of a sample of newly produced fission products is dominated by the many emissions of a very few high-yield isotopes. Specilkally, {sup 132}Te (3.2 d), its daughter, {sup 132}I(2 .28 h), {sup 140}Ba (12.75 d), and its daughter {sup 140}La (1.68 d) emit at least 18 gamma rays above 100 keV that are greater than 5% abundance. Additionally, the 1596 keV emission fiom I4'La imposes a Compton background that hinders the detection of isotopes that are neither subject to matrix dependent fractionation nor gaseous or volatile recursors. Some of these isotopes of interest are {sup 111}Ag, {sup 115}Cd, and the rare earths, {sup 153}Sm, {sup 154}Eu, {sup 156}Eu, and {sup 160}Tb. C-INC has performed an HEU irradiation and also 'cold' carrier analyses by ICP-AES to determine methods for rapid and reliable separations that may be used to detect and quantify low-yield fission products by gamma spectroscopy. Results and progress will be presented.

  6. Energy and Angular Correlations of Fission Products

    NASA Astrophysics Data System (ADS)

    Peters, William; Smith, M. S.; Pain, S. D.; Febbraro, M.; Galindo-Uribarri, A.; Jones, K. L.; Smith, K.; Grzywacz, R.; Temanson, E.; Cizewski, J. A.

    2016-09-01

    Despite the discovery of fission nearly 80 years ago and its importance to nuclear energy, national security, and astrophysics; there are very few measurements that correlate multiple fission products. A proof-of-principle experiment is underway at Oak Ridge National Lab to measure the energy and angle correlation between prompt fission neutrons, gamma rays, and fragments in time-coincidence. The angular and energy spectrum of the prompt neutrons and /or gamma rays with respect to fragment mass, could reveal new details concerning the energy balance between these products and will be essential for benchmarking advanced fission models. An array of neutron and gamma-ray detectors is positioned opposite dual time-of-flight detectors and a total-energy detector to determine one fragment mass. Preliminary results from a spontaneous 252Cf source will be presented, along with plans for future improvements. Research sponsored in part by the Laboratory Directed Research and Development Program of Oak Ridge National Laboratory, managed by UT-Battelle, LLC, for the U.S. Department of Energy.

  7. REMOVAL OF FISSION PRODUCTS FROM WATER

    DOEpatents

    Rosinski, J.

    1961-12-19

    A process is given for precipitating fission products from a body of water having a pH of above 6.5. Calcium permanganate and ferrous sulfate are added in a molar ratio of l: 3, whereby a mixed precipitate of manganese dioxide, ferric hydroxide and calcium sulfate is formed; the precipitate carries the fisston products and settles to the bottom of the body of water. (AEC)

  8. Recent MELCOR and VICTORIA Fission Product Research at the NRC

    SciTech Connect

    Bixler, N.E.; Cole, R.K.; Gauntt, R.O.; Schaperow, J.H.; Young, M.F.

    1999-01-21

    The MELCOR and VICTORIA severe accident analysis codes, which were developed at Sandia National Laboratories for the U. S. Nuclear Regulatory Commission, are designed to estimate fission product releases during nuclear reactor accidents in light water reactors. MELCOR is an integrated plant-assessment code that models the key phenomena in adequate detail for risk-assessment purposes. VICTORIA is a more specialized fission- product code that provides detailed modeling of chemical reactions and aerosol processes under the high-temperature conditions encountered in the reactor coolant system during a severe reactor accident. This paper focuses on recent enhancements and assessments of the two codes in the area of fission product chemistry modeling. Recently, a model for iodine chemistry in aqueous pools in the containment building was incorporated into the MELCOR code. The model calculates dissolution of iodine into the pool and releases of organic and inorganic iodine vapors from the pool into the containment atmosphere. The main purpose of this model is to evaluate the effect of long-term revolatilization of dissolved iodine. Inputs to the model include dose rate in the pool, the amount of chloride-containing polymer, such as Hypalon, and the amount of buffering agents in the containment. Model predictions are compared against the Radioiodine Test Facility (RTF) experiments conduced by Atomic Energy of Canada Limited (AECL), specifically International Standard Problem 41. Improvements to VICTORIA's chemical reactions models were implemented as a result of recommendations from a peer review of VICTORIA that was completed last year. Specifically, an option is now included to model aerosols and deposited fission products as three condensed phases in addition to the original option of a single condensed phase. The three-condensed-phase model results in somewhat higher predicted fission product volatilities than does the single-condensed-phase model. Modeling of U02

  9. A model for nonvolatile fission product release during reactor accident conditions

    SciTech Connect

    Lewis, B.J.; Andre, B.; Ducros, G.; Maro, D.

    1996-10-01

    An analytical model has been developed to describe the release kinetics of nonvolatile fission products (e.g., molybdenum, cerium, ruthenium, and barium) from uranium dioxide fuel under severe reactor accident conditions. This treatment considers the rate-controlling process of release in accordance with diffusional transport in the fuel matrix and fission product vaporization from the fuel surface into the surrounding gas atmosphere. The effect of the oxygen potential in the gas atmosphere on the chemical form and volatility of the fission product is considered. A correlation is also developed to account for the trapping effects of antimony and tellurium in the Zircaloy cladding. This model interprets the release behavior of fission products observed in Commissariat a l`Energie Atomique experiments conducted in the HEVA/VERCORS facility at high temperature in a hydrogen and steam atmosphere.

  10. Fission Product Release from SLOWPOKE-2 Reactors

    NASA Astrophysics Data System (ADS)

    Harnden, Anne M. C.

    Increasing radiation fields at several SLOWPOKE -2 reactors fuelled with highly enriched uranium aluminum alloy fuel have begun to interfere with the daily operation of these reactors. To investigate this phenomenon, samples of reactor container water and gas from the headspace above the reactor were obtained at four SLOWPOKE-2 reactor facilities and examined by gamma ray spectroscopy methods. These radiation fields are due to the circulation of fission products within the reactor container vessel. The most likely source of the fission product release is an area of uranium-bearing material exposed to the coolant at the end weld line which originated at the time of fuel fabrication. The results of this study are compared with observations from an underwater visual examination of one core and the metallographic examination of archived fuel elements.

  11. Thermochemistry of selected fission product compounds

    NASA Astrophysics Data System (ADS)

    Ball, R. G. J.; Bowsher, B. R.; Cordfunke, E. H. P.; Dickinson, S.; Konings, R. J. M.

    Thermochemical data have been determined for a number of compounds of fission products and reactor materials. Critical assessments have also been made of the available thermochemical data on a number of systems. The studies have focused on the vaporization of iodides, such as indium iodide and cadmium iodide, and of ternary oxide compounds, such as caesium ruthenate, borate, molybdate and phosphate. The thermodynamic properties of condensed phases such as CdI 2, Cs 2CdI 4, Cs 2RuO 4, Cs 2Si 4O 9 and Cs 2ZrO 3 have also been measured. The data enable the speciation of fission products and their transport in the event of a severe reactor accident to be predicted with greater confidence.

  12. SPIDER Progress Towards High Resolution Correlated Fission Product Data

    NASA Astrophysics Data System (ADS)

    Shields, Dan; Meierbachtol, Krista; Tovesson, Fredrik; Arnold, Charles; Blackeley, Rick; Bredeweg, Todd; Devlin, Matt; Hecht, Adam; Jandel, Marian; Jorgenson, Justin; Nelson, Ron; White, Morgan; Spider Team

    2014-09-01

    The SPIDER detector (SPectrometer for Ion DEtermination in fission Research) is under development with the goal of obtaining high-resolution, high-efficiency, correlated fission product data needed for many applications including the modeling of next generation nuclear reactors, stockpile stewardship, and the fundamental understanding of the fission process. SPIDER simultaneously measures velocity and energy of both fission products to calculate fission product yields (FPYs), neutron multiplicity (ν), and total kinetic energy (TKE). A detailed description of the prototype SPIDER detector components will be presented. Characterization measurements with alpha and spontaneous fission sources will also be discussed. LA-UR-14-24875. The SPIDER detector (SPectrometer for Ion DEtermination in fission Research) is under development with the goal of obtaining high-resolution, high-efficiency, correlated fission product data needed for many applications including the modeling of next generation nuclear reactors, stockpile stewardship, and the fundamental understanding of the fission process. SPIDER simultaneously measures velocity and energy of both fission products to calculate fission product yields (FPYs), neutron multiplicity (ν), and total kinetic energy (TKE). A detailed description of the prototype SPIDER detector components will be presented. Characterization measurements with alpha and spontaneous fission sources will also be discussed. LA-UR-14-24875. This work is in part supported by LANL Laboratory Directed Research and Development Projects 20110037DR and 20120077DR.

  13. Nuclear Fission and Fission{minus}Product Spectroscopy: Second International Workshop. Proceedings

    SciTech Connect

    Fioni, G.; Faust, H.; Oberstedt, S.; Hambsch, F.

    1998-10-01

    These proceedings represent papers presented at the Second International Workshop on Nuclear Fission and Fission{minus}Product Spectroscopy held in Seyssins, France in April, 1998. The objective was to bring together the specialists in the field to overview the situation and to assess our present understanding of the fission process. The topics presented at the conference included nuclear waste management, incineration, neutron driven transmutation, leakage etc., radioactive beams, neutron{minus}rich nuclei, neutron{minus}induced and spontaneous fission, ternary fission phenomena, angular momentum, parity and time{minus}reversal phenomena, and nuclear fission at higher excitation energy. Modern spectroscopic tools for gamma spectroscopy as applied to fission were also discussed. There were 53 papers presented at the conference,out of which 3 have been abstracted for the Energy,Science and Technology database.(AIP)

  14. Time dependent particle emission from fission products

    SciTech Connect

    Holloway, Shannon T; Kawano, Toshihiko; Moller, Peter

    2010-01-01

    Decay heating following nuclear fission is an important factor in the design of nuclear facilities; impacting a variety of aspects ranging from cooling requirements to shielding design. Calculations of decay heat, often assumed to be a simple product of activity and average decay product energy, are complicated by the so called 'pandemonium effect'. Elucidated in the 1970's this complication arises from beta-decays feeding high-energy nuclear levels; redistributing the available energy between betas and gammas. Increased interest in improving the theoretical predictions of decay probabilities has been, in part, motivated by the recent experimental effort utilizing the Total Absorption Gamma-ray Spectrometer (TAGS) to determine individual beta-decay transition probabilities to individual nuclear levels. Accurate predictions of decay heating require a detailed understanding of these transition probabilities, accurate representation of particle decays as well as reliable predictions of temporal inventories from fissioning systems. We will discuss a recent LANL effort to provide a time dependent study of particle emission from fission products through a combination of Quasiparticle Random Phase Approximation (QRPA) predictions of beta-decay probabilities, statistical Hauser-Feshbach techniques to obtain particle and gamma-ray emissions in statistical Hauser-Feshbach and the nuclear inventory code, CINDER.

  15. Fission product release mechanisms and pathways

    SciTech Connect

    Malinauskas, A.P.

    1981-01-01

    It is axiomatic that the severity of a nuclear reactor accident is determined by the extent of radioactivity escape which results. The main focus of site safety analyses is thus on fission product release and transport. Of all the processes involved, fission product escape from the fuel-cladding region into the primary coolant circuit is perhaps the most simple to describe; even so, it is an extremely complex function of the time/temperature history of the fuel-cladding system during an accident, since many mechanisms for release are involved. Depending upon the particular fission product species, these release mechanisms range from simple gaseous expansion processes at low temperatures to evaporation-condensation processes (aerosol formation) over molten fuel. Because of these complexities, it is convenient to subdivide the time/temperature sequence of an accident into more or less discrete phases over which specific release mechanisms dominate. Four such phases are the periods of (1) gap release, (2) meltdown release, (3) vaporization, and (4) oxidation release. This approach simplifies the problem considerably, although some loss of uniformity results. The methodology applies to BWR and PWR reactors with appropriate adaptations.

  16. ORNL studies of fission product release under LWR accident conditions

    SciTech Connect

    Osborne, M.F.; Lorenz, R.A.; Collins, J.L.

    1991-01-01

    High burnup Zircaloy-clad UO{sub 2} fuel specimens have been heated to study the release of fission products in tests simulating LWR accident conditions. The dominant variable was found to be temperature, with atmosphere, time, and burnup also being significant variables. Comparison of data from tests in steam and hydrogen, at temperatures of 2000 to 2700 K, have shown that the releases of the most volatile species (Kr, Xe, I, and Cs) are relatively insensitive to atmosphere. The releases of the less-volatile species (Sr, Mo, Ru, Sb, Te, Ba, and Eu), however, may vary by orders of magnitude depending on atmosphere. In addition, the atmosphere may drastically affect the mode and extent of fuel destruction.

  17. Data summary report for fission product release test VI-6

    SciTech Connect

    Osborne, M.F.; Lorenz, R.A.; Travis, J.R.; Webster, C.S.; Collins, J.L.

    1994-03-01

    Test VI-6 was the sixth test in the VI series conducted in the vertical furnace. The fuel specimen was a 15.2-cm-long section of a fuel rod from the BR3 reactor in Belgium. The fuel had experienced a burnup of {approximately}42 MWd/kg, with inert gas release during irradiation of {approximately}2%. The fuel specimen was heated in an induction furnace at 2300 K for 60 min, initially in hydrogen, then in a steam atmosphere. The released fission products were collected in three sequentially operated collection trains designed to facilitate sampling and analysis. The fission product inventories in the fuel were measured directly by gamma-ray spectrometry, where possible, and were calculated by ORIGEN2. Integral releases were 75% for {sup 85}Kr, 67% for {sup 129}I, 64% for {sup 125}Sb, 80% for both {sup 134}Cs and {sup 137}Cs, 14% for {sup 154}Eu, 63% for Te, 32% for Ba, 13% for Mo, and 5.8% for Sr. Of the totals released from the fuel, 43% of the Cs, 32% of the Sb, and 98% of the Eu were deposited in the outlet end of the furnace. During the heatup in hydrogen, the Zircaloy cladding melted, ran down, and reacted with some of the UO{sub 2} and fission products, especially Te and Sb. The total mass released from the furnace to the collection system, including fission products, fuel, and structural materials, was 0.57 g, almost equally divided between thermal gradient tubes and filters. The release behaviors for the most volatile elements, Kr and Cs, were in good agreement with the ORNL Diffusion Model.

  18. Energy production using fission fragment rockets

    SciTech Connect

    Chapline, G.; Matsuda, Y.

    1991-08-01

    Fission fragment rockets are nuclear reactors with a core consisting of thin fibers in a vacuum, and which use magnetic fields to extract the fission fragments from the reactor core. As an alternative to ordinary nuclear reactors, fission fragment rockets would have the following advantages: Approximately twice as efficient if one can directly convert the fission fragment energy into electricity; by reducing the buildup of a fission fragment inventory in the reactor one could avoid a Chernobyl type disaster; and collecting the fission fragments outside the reactor could simplify the waste disposal problem. 6 refs., 4 figs., 2 tabs.

  19. SEPARATION OF URANIUM, PLUTONIUM AND FISSION PRODUCTS

    DOEpatents

    Nicholls, C.M.; Wells, I.; Spence, R.

    1959-10-13

    The separation of uranium and plutonium from neutronirradiated uranium is described. The neutron-irradiated uranium is dissolved in nitric acid to provide an aqueous solution 3N in nitric acid. The fission products of the solution are extruded by treating the solution with dibutyl carbitol substantially 1.8N in nitric acid. The organic solvent phase is separated and neutralized with ammonium hydroxide and the plutonium reduced with hydroxylamine base to the trivalent state. Treatment of the mixture with saturated ammonium nitrate extracts the reduced plutonium and leaves the uranium in the organic solvent.

  20. (Fission product transport processes in reactor accidents)

    SciTech Connect

    Hodge, S.A.; Beahm, E.C.; Kress, T.S.; Malinauskas, A.P.

    1989-06-14

    The purpose of this trip was to participate in and to hold informal discussions with other participants in the International Centre for Heat and Mass Transfer (ICHMT) International Seminar on Fission Product Transport Processes held at Dubrovnik, Yugoslavia, during the week of May 22--26, 1989. There were 129 participants from 20 countries at the Seminar. The travelers delivered two invited lectures and presented four invited papers based upon NRC-sponsored work at Oak Ridge National Laboratory. One of the travelers also served as Chairman of the Session entitled Transport Phenomena in the Reactor Coolant System'' and appeared as a Panelist in the Closing Session of the Seminar.

  1. Dual-fission chamber and neutron beam characterization for fission product yield measurements using monoenergetic neutrons

    NASA Astrophysics Data System (ADS)

    Bhatia, C.; Fallin, B.; Gooden, M. E.; Howell, C. R.; Kelley, J. H.; Tornow, W.; Arnold, C. W.; Bond, E. M.; Bredeweg, T. A.; Fowler, M. M.; Moody, W. A.; Rundberg, R. S.; Rusev, G.; Vieira, D. J.; Wilhelmy, J. B.; Becker, J. A.; Macri, R.; Ryan, C.; Sheets, S. A.; Stoyer, M. A.; Tonchev, A. P.

    2014-09-01

    A program has been initiated to measure the energy dependence of selected high-yield fission products used in the analysis of nuclear test data. We present out initial work of neutron activation using a dual-fission chamber with quasi-monoenergetic neutrons and gamma-counting method. Quasi-monoenergetic neutrons of energies from 0.5 to 15 MeV using the TUNL 10 MV FM tandem to provide high-precision and self-consistent measurements of fission product yields (FPY). The final FPY results will be coupled with theoretical analysis to provide a more fundamental understanding of the fission process. To accomplish this goal, we have developed and tested a set of dual-fission ionization chambers to provide an accurate determination of the number of fissions occurring in a thick target located in the middle plane of the chamber assembly. Details of the fission chamber and its performance are presented along with neutron beam production and characterization. Also presented are studies on the background issues associated with room-return and off-energy neutron production. We show that the off-energy neutron contribution can be significant, but correctable, while room-return neutron background levels contribute less than <1% to the fission signal.

  2. SEPARATION OF PLUTONIUM FROM URANIUM AND FISSION PRODUCTS

    DOEpatents

    Boyd, G.E.; Adamson, A.W.; Schubert, J.; Russell, E.R.

    1958-10-01

    A chromatographic adsorption process is presented for the separation of plutonium from other fission products formed by the irradiation of uranium. The plutonium and the lighter element fission products are adsorbed on a sulfonated phenol-formaldehyde resin bed from a nitric acid solution containing the dissolved uranium. Successive washes of sulfuric, phosphoric, and nitric acids remove the bulk of the fission products, then an eluate of dilute phosphoric and nitric acids removes the remaining plutonium and fission products. The plutonium is selectively removed by passing this solution through zirconium phosphate, from which the plutonium is dissolved with nitric acid. This process provides a convenient and efficient means for isolating plutonium.

  3. Ceramic Hosts for Fission Products Immobilization

    SciTech Connect

    Peter C Kong

    2010-07-01

    Natural spinel, perovskite and zirconolite rank among the most leach resistant of mineral forms. They also have a strong affinity for a large number of other elements and including actinides. Specimens of natural perovskite and zirconolite were radioisotope dated and found to have survived at least 2 billion years of natural process while still remain their loading of uranium and thorium . Developers of the Synroc waste form recognized and exploited the capability of these minerals to securely immobilize TRU elements in high-level waste . However, the Synroc process requires a relatively uniform input and hot pressing equipment to produce the waste form. It is desirable to develop alternative approaches to fabricate these durable waste forms to immobilize the radioactive elements. One approach is using a high temperature process to synthesize these mineral host phases to incorporate the fission products in their crystalline structures. These mineral assemblages with immobilized fission products are then isolated in a durable high temperature glass for periods measured on a geologic time scale. This is a long term research concept and will begin with the laboratory synthesis of the pure spinel (MgAl2O4), perovskite (CaTiO3) and zirconolite (CaZrTi2O7) from their constituent oxides. High temperature furnace and/or thermal plasma will be used for the synthesis of these ceramic host phases. Nonradioactive strontium oxide will be doped into these ceramic phases to investigate the development of substitutional phases such as Mg1-xSrxAl2O4, Ca1-xSrxTiO3 and Ca1-xSrxZrTi2O7. X-ray diffraction will be used to establish the crystalline structures of the pure ceramic hosts and the substitution phases. Scanning electron microscopy and energy dispersive X-ray analysis (SEM-EDX) will be performed for product morphology and fission product surrogates distribution in the crystalline hosts. The range of strontium doping is planned to reach the full substitution of the divalent

  4. Immobilization of fission products in phosphate ceramic waste forms

    SciTech Connect

    Singh, D.

    1996-10-01

    The goal of this project is to develop and demonstrate the feasibility of a novel low-temperature solidification/stabilization (S/S) technology for immobilizing waste streams containing fission products such as cesium, strontium, and technetium in a chemically bonded phosphate ceramic. This technology can immobilize partitioned tank wastes and decontaminate waste streams containing volatile fission products.

  5. SEPARATION OF FISSION PRODUCTS FROM PLUTONIUM BY PRECIPITATION

    DOEpatents

    Seaborg, G.T.; Thompson, S.G.; Davidson, N.R.

    1959-09-01

    Fission product separation from hexavalent plutonium by bismuth phosphate precipitation of the fission products is described. The precipitation, according to this invention, is improved by coprecipitating ceric and zirconium phosphates (0.05 to 2.5 grams/liter) with the bismuth phosphate.

  6. REGENERATION OF FISSION-PRODUCT-CONTAINING MAGNESIUM-THORIUM ALLOYS

    DOEpatents

    Chiotti, P.

    1964-02-01

    A process of regenerating a magnesium-thorium alloy contaminated with fission products, protactinium, and uranium is presented. A molten mixture of KCl--LiCl-MgCl/sub 2/ is added to the molten alloy whereby the alkali, alkaline parth, and rare earth fission products (including yttrium) and some of the thorium and uranium are chlorinated and

  7. Chemical factors affecting fission product transport in severe LMFBR accidents

    SciTech Connect

    Wichner, R.P.; Jolley, R.L.; Gat, U.; Rodgers, B.R.

    1984-10-01

    This study was performed as a part of a larger evaluation effort on LMFBR accident, source-term estimation. Purpose was to provide basic chemical information regarding fission product, sodium coolant, and structural material interactions required to perform estimation of fission product transport under LMFBR accident conditions. Emphasis was placed on conditions within the reactor vessel; containment vessel conditions are discussed only briefly.

  8. (Fuel, fission product, and graphite technology)

    SciTech Connect

    Stansfield, O.M.

    1990-07-25

    Travel to the Forschungszentrum (KFA) -- Juelich described in this report was for the purpose of participating in the annual meeting of subprogram managers for the US/DOE Umbrella Agreement for Fuel, Fission Product, and Graphite Technology. At this meeting the highlights of the cooperative exchange were reviewed for the time period June 1989 through June 1990. The program continues to contribute technology in an effective way for both countries. Revision 15 of the Subprogram Plan will be issued as a result of the meeting. There was interest expressed by KFA management in the level of support received from the NPR program and in potential participation in the COMEDIE loop experiment being conducted at the CEA.

  9. Chemistry of fission product iodine under nuclear reactor accident conditions

    SciTech Connect

    Malinauskas, A.P.; Bell, J.T.

    1986-01-01

    The radioisotopes of iodine are generally acknowledged to be the species whose release into the biosphere as a result of a nuclear reactor accident is of the greatest concern. In the course of its release, the fission product is subjected to differing chemical environments; these can alter the physicochemical form of the fission product and thus modify the manner and extent to which release occurs. Both the chemical environments which are characteristic of reactor accidents and their effect in determining physical and chemical form of fission product iodine have been studied extensively, and are reviewed in this report. 76 refs.

  10. Chemical state of fission products in irradiated uranium carbide fuel

    NASA Astrophysics Data System (ADS)

    Arai, Yasuo; Iwai, Takashi; Ohmichi, Toshihiko

    1987-12-01

    The chemical state of fission products in irradiated uranium carbide fuel has been estimated by equilibrium calculation using the SOLGASMIX-PV program. Solid state fission products are distributed to the fuel matrix, ternary compounds, carbides of fission products and intermetallic compounds among the condensed phases appearing in the irradiated uranium carbide fuel. The chemical forms are influenced by burnup as well as stoichiometry of the fuel. The results of the present study almost agree with the experimental ones reported for burnup simulated carbides.

  11. Distribution of fission products in an LMFBR: summary

    SciTech Connect

    Villarreal, R.; Young, J.O.

    1985-01-01

    The overall distribution of fission products released from experimental subassemblies containing breached fuel elements has been determined in the fuel and throughout the EBR-II primary and secondary reactor systems. Identification of the fission products released to the primary sodium and location of areas of concentration was important in anticipating radioactive species and levels of deposited fission and activation products on components removed from the primary tank for maintenance and repair. The results of extensive radioanalytical measurements on the fuel, fuel cladding, primary sodium and cover gas system, secondary sodium and cover gas system and steam system are summarized.

  12. Fission product yield measurements using monoenergetic photon beams

    NASA Astrophysics Data System (ADS)

    Krishichayan; Bhike, M.; Tonchev, A. P.; Tornow, W.

    2017-09-01

    Measurements of fission products yields (FPYs) are an important source of information on the fission process. During the past couple of years, a TUNL-LANL-LLNL collaboration has provided data on the FPYs from quasi monoenergetic neutron-induced fission on 235U, 238U, and 239Pu and has revealed an unexpected energy dependence of both asymmetric fission fragments at energies below 4 MeV. This peculiar FPY energy dependence was more pronounced in neutron-induced fission of 239Pu. In an effort to understand and compare the effect of the incoming probe on the FPY distribution, we have carried out monoenergetic photon-induced fission experiments on the same 235U, 238U, and 239Pu targets. Monoenergetic photon beams of Eγ = 13.0 MeV were provided by the HIγS facility, the world's most intense γ-ray source. In order to determine the total number of fission events, a dual-fission chamber was used during the irradiation. These irradiated samples were counted at the TUNL's low-background γ-ray counting facility using high efficient HPGe detectors over a period of 10 weeks. Here we report on our first ever photofission product yield measurements obtained with monoenegetic photon beams. These results are compared with neutron-induced FPY data.

  13. Fission Product Transmutation in Mixed Radiation Fields

    SciTech Connect

    Harmon, Frank; Burgett, Erick; Starovoitova, Valeriia; Tsveretkov, Pavel

    2015-01-15

    Work under this grant addressed a part of the challenge facing the closure of the nuclear fuel cycle; reducing the radiotoxicity of lived fission products (LLFP). It was based on the possibility that partitioning of isotopes and accelerator-based transmutation on particular LLFP combined with geological disposal may lead to an acceptable societal solution to the problem of management. The feasibility of using photonuclear processes based on the excitation of the giant dipole resonance (GDR) by bremsstrahlung radiation as a cost effective transmutation method was accessed. The nuclear reactions of interest: (γ,xn), (n,γ), (γ,p) can be induced by bremsstrahlung radiation produced by high power electron accelerators. The driver of these processes would be an accelerator that produces a high energy and high power electron beam of ~ 100 MeV. The major advantages of such accelerators for this purpose are that they are essentially available “off the shelf” and potentially would be of reasonable cost for this application. Methods were examined that used photo produced neutrons or the bremsstrahlung photons only, or use both photons and neutrons in combination for irradiations of selected LLFP. Extrapolating the results to plausible engineering scale transmuters it was found that the energy cost for 129I and 99Tc transmutation by these methods are about 2 and 4%, respectively, of the energy produced from 1000MWe.

  14. Thermodynamics of fission products in UO2+-x

    SciTech Connect

    Nerikar, Pankaj V

    2009-01-01

    The stabilities of selected fission products - Xe, Cs, and Sr - are investigated as a function of non-stoichiometry x in UO{sub 2{+-}x}. In particular, density functional theory (OFT) is used to calculate the incorporation and solution energies of these fission products at the anion and cation vacancy sites, at the divacancy, and at the bound Schottky defect. In order to reproduce the correct insulating state of UO{sub 2}, the DFT calculations are performed using spin polarization and with the Hubbard U tenn. In general, higher charge defects are more soluble in the fuel matrix and the solubility of fission products increases as the hyperstoichiometry increases. The solubility of fission product oxides is also explored. CS{sub 2}O is observed as a second stable phase and SrO is found to be soluble in the UO{sub 2} matrix for all stoichiometries. These observations mirror experimentally observed phenomena.

  15. Data summary report for fission product release test VI-4

    SciTech Connect

    Obsorne, M.F.; Lorenz, R.A.; Collins, J.L.; Travis, J.R.; Webster, C.S.; Nakamura, T. )

    1991-01-01

    This was the fourth in a series of high-temperature fission product release tests in a vertical test apparatus. The test specimen, a 15.2-cm-long section of a fuel rod from the BR3 reactor in Belgium, had been irradiated to a burnup of 47 MWd/kg. In simulation of a severe accident in a light-water reactor, it was heated in hydrogen in a hot cell-mounted test apparatus to a maximum test temperature of 2400 K for a period of 20 min. The released fission products were collected on components designed to facilitate sampling and analysis. On-line radioactivity measurements and posttest inspection revealed that the fuel had partially collapsed at about the time the cladding melted. Based on fission product inventories measured in the fuel or calculated by ORIGEN2, analyses of test components showed total releases from the fuel of 85% for {sup 85}Kr, <1% for {sup 106}Ru, 3.9% for {sup 125}Sb, 96% for both {sup 134}Cs and {sup 137}Cs, and 13% for {sup 154}Eu. Large fractions of the released fission products (up to 96% of the {sup 154}Eu) were retained in the furnace. Small release fractions for several other fission products -- Rb, Br, Sr, Te, I, and Ba -- were detected also. In addition, very small amounts of fuel material -- uranium and plutonium -- were released. Total mass release from the furnace to the collection system, which included fission products, fuel material, and structural materials, was 0.40g, with 40% of this material being deposited as vapor and 60% of it being collected as aerosols. The results from this test were compared with previous tests in this series and with an in-pile test at similar conditions at Sandia National Laboratories. There was no indication that the mode of heating (fission heat vs radiant heat) significantly affected fission product release. 24 refs., 25 figs., 14 tabs.

  16. Spent Nuclear Fuel project estimate of volatile fission products release from multi-canister overpacks

    SciTech Connect

    Cooper, T.D.

    1996-08-01

    Spent N-Reactor fuel will be moved from wet pool storage to dry storage at Hanford Washington. This fuel will be sequentially loaded into a Multiple Container Overpack (MCO), moved to the cold vacuum drying station, drained, cold vacuum dried, shipped to the Canister Storage Building (CSB), staged for up to 2 years,hot vacuum dried at 300 degrees C, hot conditioned at 150 degrees C, and finally, sealed and stored for up to 75 years in the CSB.During each proposed process step, the volatile radioactive fission products released to the atmosphere were estimated.Tritium is the only volatile fission product released insignificant amounts during each process step. For an accident scenario involving interior MCO temperature of 600 degrees C for up to 8 hours, it was estimated that many volatile fission products are released.

  17. Transmutation of fission products and actinide waste at Hanford

    SciTech Connect

    Daemen, L.L.; Pitcher, E.J.; Russell, G.J.

    1995-10-01

    The authors studied the neutronics of an ATW system for the transmutation of the fission products ({sup 99}Tc in particular) and the type of actinide waste stored in several tanks at Hanford. The heart of the system is a highly-efficient neutron production target. It is surrounded by a blanket containing a moderator/reflector material, as well as the products to be transmuted. The fission products are injected into the blanket in the form of an aqueous solution in heavy water, whereas an aqueous actinides slurry is circulated in the outer part of the blanket. For the sake of definiteness, the authors focussed on {sup 99}Tc (the most difficult fission product to transmute), and {sup 239}Pu, {sup 237}Np, and {sup 241}Am. Because of the low thermal neutron absorption cross-section of {sup 99}Tc, considerable care and effort must be devoted to the design of a very efficient neutron source.

  18. Early results utilizing high-energy fission product (gamma) rays to detect fissionable material in cargo

    SciTech Connect

    Slaughter, D R; Accatino, M R; Bernstein, A; Church, J A; Descalle, M A; Gosnell, T B; Hall, J M; Loshak, A; Manatt, D R; Mauger, G J; McDowell, M; Moore, T M; Norman, E B; Pohl, B A; Pruet, J A; Petersen, D C; Walling, R S; Weirup, D L; Prussin, S G

    2004-09-30

    A concept for detecting the presence of special nuclear material ({sup 235}U or {sup 239}Pu) concealed in intermodal cargo containers is described. It is based on interrogation with a pulsed beam of 7 MeV neutrons that produce fission events and their {beta}-delayed neutron emission or {beta}-delayed high-energy {gamma}-radiation between beam pulses provide the detection signature. Fission product {beta}-delayed {gamma}-rays above 3 MeV are nearly ten times more abundant than {beta}-delayed neutrons and are distinct from natural radioactivity and from nearly all of the induced activity in a normal cargo. Detector backgrounds and potential interferences with the fission signature radiation have been identified and quantified. An important goal in the US is the detection of nuclear weapons or special nuclear material (SNM) concealed in intermodal cargo containers. This must be done with high detection probability, low false alarm rates, and without impeding commerce, i.e. about one minute for an inspection. The concept for inspection has been described before and its components are now being evaluated. While normal radiations emitted from plutonium may allow its detection, the majority of {sup 235}U {gamma} ray emission is at 186 keV, is readily attenuated by cargo, and thus not a reliable detection signature for passive detection. Delayed neutron detection following a neutron or photon beam pulse has been used successfully to detect lightly or unshielded SNM targets. While delayed neutrons can be easily distinguished from beam neutrons they have relatively low yield in fission, approximately 0.008 per fission in {sup 239}Pu and 0.017 per fission in {sup 235}U, and are rapidly attenuated in hydrogenous materials making that technique unreliable when challenged by thick hydrogenous cargo overburden. They propose detection of {beta}-delayed high-energy {gamma} radiation as a more robust signature characteristic of SNM.

  19. Evaluation and compilation of fission product yields 1993

    SciTech Connect

    England, T.R.; Rider, B.F.

    1995-12-31

    This document is the latest in a series of compilations of fission yield data. Fission yield measurements reported in the open literature and calculated charge distributions have been used to produce a recommended set of yields for the fission products. The original data with reference sources, and the recommended yields axe presented in tabular form. These include many nuclides which fission by neutrons at several energies. These energies include thermal energies (T), fission spectrum energies (F), 14 meV High Energy (H or HE), and spontaneous fission (S), in six sets of ten each. Set A includes U235T, U235F, U235HE, U238F, U238HE, Pu239T, Pu239F, Pu241T, U233T, Th232F. Set B includes U233F, U233HE, U236F, Pu239H, Pu240F, Pu241F, Pu242F, Th232H, Np237F, Cf252S. Set C includes U234F, U237F, Pu240H, U234HE, U236HE, Pu238F, Am241F, Am243F, Np238F, Cm242F. Set D includes Th227T, Th229T, Pa231F, Am241T, Am241H, Am242MT, Cm245T, Cf249T, Cf251T, Es254T. Set E includes Cf250S, Cm244S, Cm248S, Es253S, Fm254S, Fm255T, Fm256S, Np237H, U232T, U238S. Set F includes Cm243T, Cm246S, Cm243F, Cm244F, Cm246F, Cm248F, Pu242H, Np237T, Pu240T, and Pu242T to complete fission product yield evaluations for 60 fissioning systems in all. This report also serves as the primary documentation for the second evaluation of yields in ENDF/B-VI released in 1993.

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

    NASA Astrophysics Data System (ADS)

    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.

    2010-12-01

    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 99Mo, 95Zr, 137Cs, 140Ba, 141,143Ce, and 147Nd. Modest incident-energy dependence exists for the 147Nd 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 ˜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 99Mo

  1. Comparison of Fission Product Yields and Their Impact

    SciTech Connect

    S. Harrison

    2006-02-01

    This memorandum describes the Naval Reactors Prime Contractor Team (NRPCT) Space Nuclear Power Program (SNPP) interest in determining the expected fission product yields from a Prometheus-type reactor and assessing the impact of these species on materials found in the fuel element and balance of plant. Theoretical yield calculations using ORIGEN-S and RACER computer models are included in graphical and tabular form in Attachment, with focus on the desired fast neutron spectrum data. The known fission product interaction concerns are the corrosive attack of iron- and nickel-based alloys by volatile fission products, such as cesium, tellurium, and iodine, and the radiological transmutation of krypton-85 in the coolant to rubidium-85, a potentially corrosive agent to the coolant system metal piping.

  2. Fission products behaviour during a power transient: Their inventory in an intragranular bubble

    NASA Astrophysics Data System (ADS)

    Desgranges, L.; Blay, Th.; Lamontagne, J.; Roure, I.; Bienvenu, Ph.

    2017-09-01

    The behaviour of fission products is a key issue during Anticipated Operational Occurrences (AOOs) or Condition II transients or accidental sequence for nuclear fuel. Here we characterized how fission products behaved inside chromium doped UO2 pellet during a power ramp. At the pellet centre fission products have left the UO2 lattice and can be found in bubbles. The composition of the bubbles was determined using an original experimental methodology. The existence of separated precipitates made of metallic fission products for the one, and volatile fission products for the other, was evidenced. This result is discussed with regards to the behaviour of fission products during a power ramp.

  3. Atmospheric Chemistry Data Products

    NASA Technical Reports Server (NTRS)

    2003-01-01

    This presentation poster covers data products from the Distributed Active Archive Center (DAAC) of the Goddard Earth Sciences (GES) Data and Information Services Center (DISC). Total Ozone Mapping Spectrometer products (TOMS) introduced in the presentation include TOMS Version 8 as well as Aura, which provides 25 years of TOMS and Upper Atmosphere Research Satellite (UARS) data. The presentation lists a number of atmospheric chemistry and dynamics data sets at DAAC.

  4. Anomalous Xenon in the Precambrian Nuclear Reactor in Okelobondo (Gabon): A Possible Connection to the Fission Component in the Terrestrial Atmosphere

    NASA Technical Reports Server (NTRS)

    Meshik, A. P.; Kehm, K.; Hohenberg, C. M.

    1999-01-01

    Some CFF-Xe (Chemically Fractionated Fission Xenon), whose isotopic composition is established by simultaneous decay and migration of radioactive fission products, is probably present in the Earth's lithosphere, a conclusion based on available Xe data from various crustal and mantle rocks . Our recent isotopic analysis of Xe in alumophosphate from zone 13 of Okelobondo (southern extension of Oklo), along with the independent estimation of the isotopic composition of atmospheric fission Xe , supports the hypothesis that CFF-Xe was produced on a planetary scale. Additional information is contained in the original extended abstract.

  5. Anomalous Xenon in the Precambrian Nuclear Reactor in Okelobondo (Gabon): A Possible Connection to the Fission Component in the Terrestrial Atmosphere

    NASA Technical Reports Server (NTRS)

    Meshik, A. P.; Kehm, K.; Hohenberg, C. M.

    1999-01-01

    Some CFF-Xe (Chemically Fractionated Fission Xenon), whose isotopic composition is established by simultaneous decay and migration of radioactive fission products, is probably present in the Earth's lithosphere, a conclusion based on available Xe data from various crustal and mantle rocks . Our recent isotopic analysis of Xe in alumophosphate from zone 13 of Okelobondo (southern extension of Oklo), along with the independent estimation of the isotopic composition of atmospheric fission Xe , supports the hypothesis that CFF-Xe was produced on a planetary scale. Additional information is contained in the original extended abstract.

  6. Data summary report for fission product release Test VI-7

    SciTech Connect

    Osborne, M.F.; Lorentz, R.A.; Travis, J.R.; Collins, J.L.; Webster, C.S.

    1995-05-01

    Test VI-7 was the final test in the VI series conducted in the vertical furnace. The fuel specimen was a 15.2-cm-long section of a fuel rod from the Monticello boiling water reactor (BWR). The fuel had experienced a burnup of {approximately}-40 Mwd/kg U. It was heated in an induction furnace for successive 20-min periods at 2000 and 2300 K in a moist air-helium atmosphere. Integral releases were 69% for {sup 85}Kr, 52% for {sup 125}Sb, 71% for both {sup 134}Cs and {sup 137}Cs, and 0.04% for {sup 154}Eu. For the non-gamma-emitting species, release values for 42% for I, 4.1% for Ba, 5.3% for Mo, and 1.2% for Sr were determined. The total mass released from the furnace to the collection system, including fission products, fuel, and structural materials, was 0.89 g, with 37% being collected on the thermal gradient tubes and 63% downstream on filters. Posttest examination of the fuel specimen indicated that most of the cladding was completely oxidized to ZrO{sub 2}, but that oxidation was not quite complete at the upper end. The release behaviors for the most volatile elements, Kr and Cs, were in good agreement with the ORNL-Booth Model.

  7. Correlations for fission product release from N Reactor fuel under high-temperature accident conditions

    SciTech Connect

    Birney, K.R.; Bechtold, D.B.; McCall, T.B.

    1988-03-01

    Empirical correlations were derived for fission product release from metallic uranium alloy 601 N Reactor fuel during postulated accident conditions in which the fuel nears, reaches, or exceeds the melting temperature. The correlations were based on a sparse data base from fuel melted in an inert or steam atmosphere. The empirical correlations are presented for use in subsequent deterministic analyses of N Reactor behavior during hypothetical severe accidents beyond the design basis. 20 refs., 4 figs., 4 tabs.

  8. Fission Product Yields from Fission Spectrum n+ 239Pu for ENDF/B-VII.1

    NASA Astrophysics Data System (ADS)

    Chadwick, M. B.; Kawano, T.; Barr, D. W.; Mac Innes, M. R.; Kahler, A. C.; Graves, T.; Selby, H.; Burns, C. J.; Inkret, W. C.; Keksis, A. L.; Lestone, J. P.; Sierk, A. J.; Talou, P.

    2010-12-01

    We describe a new cumulated fission product yield (FPY) evaluation for fission spectrum neutrons on plutonium that updates the ENDF/B-VI evaluation by England and Rider, for the forthcoming ENDF/B-VII.1 database release. We focus on FPs that are needed for high accuracy burnup assessments; that is, for inferring the number of fissions in a neutron environment. Los Alamos conducted an experiment in the 1970s in the Bigten fast critical assembly to determine fission product yields as part of the Interlaboratory Reaction Rate (ILRR) collaboration, and this has defined the Laboratory's fission standard to this day. Our evaluation includes use of the LANL-ILRR measurements (not previously available to evaluators) as well as other Laboratory FPY measurements published in the literature, especially the high-accuracy mass spectrometry data from Maeck and others. Because the measurement database for some of the FPs is small — especially for 99Mo — we use a meta-analysis that incorporates insights from other accurately-measured benchmark FP data, using R-value ratio measurements. The meta-analysis supports the FP measurements from the LANL-ILRR experiment. Differences between our new evaluations and ENDF/B-VI are small for some FPs (less than 1-2%-relative for 95Zr, 140Ba, 144Ce), but are larger for 99Mo (4%-relative) and 147Nd (5%-relative, at 1.5 MeV) respectively. We present evidence for an incident neutron energy dependence to the 147Nd fission product yield that accounts for observed differences in the FPY at a few-hundred keV average energy in fast reactors versus measurements made at higher average neutron energies in Los Alamos' fast critical assemblies. Accounting for such FPY neutron energy dependencies is important if one wants to reach a goal of determining the number of fissions to accuracies of 1-2%. An evaluation of the energy-dependence of fission product yields is given for all A values based on systematical trends in the measured data, with a focus on

  9. A Covariance Generation Methodology for Fission Product Yields

    NASA Astrophysics Data System (ADS)

    Terranova, N.; Serot, O.; Archier, P.; Vallet, V.; De Saint Jean, C.; Sumini, M.

    2016-03-01

    Recent safety and economical concerns for modern nuclear reactor applications have fed an outstanding interest in basic nuclear data evaluation improvement and completion. It has been immediately clear that the accuracy of our predictive simulation models was strongly affected by our knowledge on input data. Therefore strong efforts have been made to improve nuclear data and to generate complete and reliable uncertainty information able to yield proper uncertainty propagation on integral reactor parameters. Since in modern nuclear data banks (such as JEFF-3.1.1 and ENDF/BVII.1) no correlations for fission yields are given, in the present work we propose a covariance generation methodology for fission product yields. The main goal is to reproduce the existing European library and to add covariance information to allow proper uncertainty propagation in depletion and decay heat calculations. To do so, we adopted the Generalized Least Square Method (GLSM) implemented in CONRAD (COde for Nuclear Reaction Analysis and Data assimilation), developed at CEA-Cadarache. Theoretical values employed in the Bayesian parameter adjustment are delivered thanks to a convolution of different models, representing several quantities in fission yield calculations: the Brosa fission modes for pre-neutron mass distribution, a simplified Gaussian model for prompt neutron emission probability, theWahl systematics for charge distribution and the Madland-England model for the isomeric ratio. Some results will be presented for the thermal fission of U-235, Pu-239 and Pu-241.

  10. SEPARATION OF PLUTONIUM FROM URANIUM AND FISSION PRODUCTS BY ADSORPTION

    DOEpatents

    Seaborg, G.T.; Willard, J.E.

    1958-01-01

    A method is presented for the separation of plutonium from solutions containing that element in a valence state not higher than 41 together with uranium ions and fission products. This separation is accomplished by contacting the solutions with diatomaceous earth which preferentially adsorbs the plutonium present. Also mentioned as effective for this adsorbtive separation are silica gel, filler's earth and alumina.

  11. Applications for fission product data to problems in stellar nucleosynthesis

    SciTech Connect

    Mathews, G.J.

    1983-10-01

    A general overview of the nucleosynthesis mechanisms for heavy (A greater than or equal to 70) nuclei is presented with particular emphasis on critical data needs. The current state of the art in nucleosynthesis models is described and areas in which fission product data may provide useful insight are proposed. 33 references, 10 figures.

  12. Data summary report for fission product release test VI-5

    SciTech Connect

    Osborne, M.F.; Lorenz, R.A.; Travis, J.R.; Webster, C.S.; Collins, J.L. )

    1991-10-01

    Test VI-5, the fifth in a series of high-temperature fission product release tests in a vertical test apparatus, was conducted in a flowing mixture of hydrogen and helium. The test specimen was a 15.2-cm-long section of a fuel rod from the BR3 reactor in Belgium which had been irradiated to a burnup of {approximately}42 MWd/kg. Using a hot cell-mounted test apparatus, the fuel rod was heated in an induction furnace under simulated LWR accident conditions to two test temperatures, 2000 K for 20 min and then 2700 K for an additional 20 min. The released fission products were collected in three sequentially operated collection trains on components designed to measure fission product transport characteristics and facilitate sampling and analysis. The results from this test were compared with those obtained in previous tests in this series and with the CORSOR-M and ORNL diffusion release models for fission product release. 21 refs., 19 figs., 12 tabs.

  13. Ab initio modelling of volatile fission products in uranium mononitride

    NASA Astrophysics Data System (ADS)

    Klipfel, M.; Van Uffelen, P.

    2012-03-01

    Defects and the incorporation of volatile fission products (xenon, krypton, caesium and iodine) in uranium mononitride are investigated using DFT calculations. Various locations for impurities are considered including at a tetrahedral interstitial position, substitution of a host nitrogen or uranium ion and placed in a Schottky defect (UN bivacancy). The incorporation is energetically more favourable for the latter, although the incorporation energies are positive. The preferred position for volatile fission products in UN is at the larger of the vacancies, either a single uranium vacancy or the uranium vacancy of a Schottky defect. The incorporation of a fission product in a bound [1 0 0]-Schottky defect leads to a tetragonal distortion of the supercell. The impurities considered in this work produce very small perturbations of the crystalline matrix of UN. With the exception of impurities at the interstitial site, which perturb the structure into the second coordination sphere, only the displacement of the atoms at the nearest-neighbour positions is significant. Analysis of the charge distribution after incorporation of the fission product reveals a weak charge transfer for the noble gases, while a larger transfer is displayed for caesium and iodine.

  14. Fission properties and production mechanisms for the heaviest known elements

    SciTech Connect

    Hoffman, D.C.

    1981-01-01

    Mass yields of the spontaneous fission of Fm isotopes, Cf isotopes, and /sup 259/Md are discussed. Actinide yields were measured for bombardments of /sup 248/Cm with /sup 16/O, /sup 18/O, /sup 20/Ne, and /sup 22/Ne. A superheavy product might be produced by bombarding /sup 248/Cm with /sup 48/Ca ions. 12 figures. (DLC)

  15. Data summary report for fission product release test VI-3

    SciTech Connect

    Osborne, M.F.; Lorenz, R.A.; Collins, J.L.; Travis, J.R.; Webster, C.S.; Lee, H.K.; Nakamura, T.; Tong, Y.-C. )

    1990-06-01

    Test VI-3, the third in a series of high-temperature fission product release tests in the vertical test apparatus, was conducted in flowing steam. The test specimen was a 15.2-cm-long section of a fuel rod from the BR3 reactor in Belgium, which had been irradiated to a burnup of 42 MWd/kg. Using an induction furnace, it was heated under simulated light-water reactor (LWR) accident conditions to two test temperatures, 20 min at 2000 K and then 20 min at 2700 K, in a hot cell-mounted test apparatus. The released fission products were collected on components designed to facilitate sampling and analysis. Posttest inspection confirmed that the cladding had been completely oxidized during the test. Only minimal fragmentation of the fuel specimen was found, however, and very little melting or fuel-cladding interaction had occurred. Based on fission product inventories measured in the fuel or calculated by ORIGEN2, analyses of test components showed total releases from the fuel of 100% for {sup 85}Kr, 5% for {sup 106}Ru, 99% for {sup 125}Sb, and 99% for both {sup 134}Cs and {sup 137}Cs. A large fraction (27%) of the released {sup 125}Sb was retained in the furnace, but most of the released cesium (89%) escaped to the collection system. In addition, very small amounts of fuel material --- uranium and plutonium --- were released. Including fission products and fuel and structural materials, the total mass released from the furnace to the collection system was 3.17 g, 78% of which was collected on the filters. The results from this test were compared with previous tests in this series and with a commonly used model for fission product release. 25 refs., 22 figs., 14 tabs.

  16. Report on simulation of fission gas and fission product diffusion in UO2

    SciTech Connect

    Andersson, Anders David; Perriot, Romain Thibault; Pastore, Giovanni; Tonks, Michael R.; Cooper, Michael William; Liu, Xiang-Yang; Goyal, Anuj; Uberuaga, Blas P.; Stanek, Christopher Richard

    2016-07-22

    In UO2 nuclear fuel, the retention and release of fission gas atoms such as xenon (Xe) are important for nuclear fuel performance by, for example, reducing the fuel thermal conductivity, causing fuel swelling that leads to mechanical interaction with the clad, increasing the plenum pressure and reducing the fuel–clad gap thermal conductivity. We use multi-­scale simulations to determine fission gas diffusion mechanisms as well as the corresponding rates in UO2 under both intrinsic and irradiation conditions. In addition to Xe and Kr, the fission products Zr, Ru, Ce, Y, La, Sr and Ba have been investigated. Density functional theory (DFT) calculations are used to study formation, binding and migration energies of small clusters of Xe atoms and vacancies. Empirical potential calculations enable us to determine the corresponding entropies and attempt frequencies for migration as well as investigate the properties of large clusters or small fission gas bubbles. A continuum reaction-­diffusion model is developed for Xe and point defects based on the mechanisms and rates obtained from atomistic simulations. Effective fission gas diffusivities are then obtained by solving this set of equations for different chemical and irradiation conditions using the MARMOT phase field code. The predictions are compared to available experimental data. The importance of the large XeU3O cluster (a Xe atom in a uranium + oxygen vacancy trap site with two bound uranium vacancies) is emphasized, which is a consequence of its high mobility and high binding energy. We find that the XeU3O cluster gives Xe diffusion coefficients that are higher for intrinsic conditions than under irradiation over a wide range of temperatures. Under irradiation the fast-­moving XeU3O cluster recombines quickly with irradiation-induced interstitial U ions, while this mechanism is less important for intrinsic conditions. The net result is higher

  17. Analysis of fission product release behavior during the TMI-2 accident

    SciTech Connect

    Petti, D. A.; Adams, J. P.; Anderson, J. L.; Hobbins, R. R.

    1987-01-01

    An analysis of fission product release during the Three Mile Island Unit 2 (TMI-2) accident has been initiated to provide an understanding of fission product behavior that is consistent with both the best estimate accident scenario and fission product results from the ongoing sample acquisition and examination efforts. ''First principles'' fission product release models are used to describe release from intact, disrupted, and molten fuel. Conclusions relating to fission product release, transport, and chemical form are drawn. 35 refs., 12 figs., 7 tabs.

  18. NEANDC specialists meeting on yields and decay data of fission product nuclides

    SciTech Connect

    Chrien, R.E.; Burrows, T.W.

    1983-01-01

    Separate abstracts were prepared for the 29 papers presented. Workshop reports on decay heat, fission yields, beta- and gamma-ray spectroscopy, and delayed neutrons are included. An appendix contains a survey of the most recent compilations and evaluations containing fission product yield, fission product decay data, and delayed neutron yield information. (WHK)

  19. Mass distribution and mass resolved angular distribution of fission products in 28Si+232Th

    NASA Astrophysics Data System (ADS)

    Sodaye, Suparna; Tripathi, R.; John, B. V.; Ramachandran, K.; Pujari, P. K.

    2017-01-01

    Background: Fission process with heavier projectiles and actinide targets has contributions from processes, such as compound nucleus fission, transfer-induced fission, and noncompound nucleus fission. Mass distribution and mass-dependent anisotropy can be used to identify and delineate the contributions due to these different processes. Purpose: Mass distribution in 28Si+232Th has been studied at beam energies of 180 and 158 MeV to investigate the nature of mass distribution arising from complete and incomplete momentum-transfer fission events. Mass-dependent angular anisotropy has been measured at 166 MeV to investigate the dominant noncompound nucleus process contributing to the fission. Method: Mass distribution and mass resolved angular distribution of fission products were measured by the recoil catcher method followed by off-line γ -ray spectrometry. Results: Mass distributions for full momentum-transfer fission processes were found to be symmetric, and those for transfer-induced fission were found to be asymmetric at both beam energies. The relative contribution from transfer-induced fission was found to be higher at lower beam energy. The anisotropy of the fission product angular distribution was found to increase with decreasing mass asymmetry. Conclusions: The mass distribution indicates that, apart from the full momentum-transfer fission process, there is a significant contribution due to transfer-induced fission. The mass dependence of angular anisotropy indicated that preequilibrium fission is the dominant noncompound nucleus process in the present reaction system at near barrier energy (Ec .m ./VC=1.06 ) .

  20. Molten salt extraction of transuranic and reactive fission products from used uranium oxide fuel

    SciTech Connect

    Herrmann, Steven Douglas

    2014-05-27

    Used uranium oxide fuel is detoxified by extracting transuranic and reactive fission products into molten salt. By contacting declad and crushed used uranium oxide fuel with a molten halide salt containing a minor fraction of the respective uranium trihalide, transuranic and reactive fission products partition from the fuel to the molten salt phase, while uranium oxide and non-reactive, or noble metal, fission products remain in an insoluble solid phase. The salt is then separated from the fuel via draining and distillation. By this method, the bulk of the decay heat, fission poisoning capacity, and radiotoxicity are removed from the used fuel. The remaining radioactivity from the noble metal fission products in the detoxified fuel is primarily limited to soft beta emitters. The extracted transuranic and reactive fission products are amenable to existing technologies for group uranium/transuranic product recovery and fission product immobilization in engineered waste forms.

  1. Chemical state of fission products in irradiated UO 2

    NASA Astrophysics Data System (ADS)

    Imoto, S.

    1986-08-01

    The chemical state of fission products in irradiated UO 2 fuel has been estimated for FBR as well as LWR on the basis of equilibrium calculation with the SOLGASMIX-PV code. The system considered for the calculation is composed of a gas phase, a CaF 2 type oxide phase, three grey phases, a noble metal alloy, a mixed telluride phase and several other phases each consisting of single compound. The distribution of elements into these phases and the amount of chemical species in each phase at different temperatures are obtained as a function of oxygen potential for LWR and FBR. Changes of the chemical potential of the fuel-fission products system during burnup are also evaluated with particular attention to the difference between LWR and FBR. Some informations obtained by the calculation are compared with the results of post irradiation examination of UO 2 fuels.

  2. Superabsorbing gel for actinide, lanthanide, and fission product decontamination

    SciTech Connect

    Kaminski, Michael D.; Mertz, Carol J.

    2016-06-07

    The present invention provides an aqueous gel composition for removing actinide ions, lanthanide ions, fission product ions, or a combination thereof from a porous surface contaminated therewith. The composition comprises a polymer mixture comprising a gel forming cross-linked polymer and a linear polymer. The linear polymer is present at a concentration that is less than the concentration of the cross-linked polymer. The polymer mixture is at least about 95% hydrated with an aqueous solution comprising about 0.1 to about 3 percent by weight (wt %) of a multi-dentate organic acid chelating agent, and about 0.02 to about 0.6 molar (M) carbonate salt, to form a gel. When applied to a porous surface contaminated with actinide ions, lanthanide ions, and/or other fission product ions, the aqueous gel absorbs contaminating ions from the surface.

  3. CONTROL CONSOLE FOR MTR FISSION PRODUCT MONITOR, USED TO DETECT ...

    Library of Congress Historic Buildings Survey, Historic Engineering Record, Historic Landscapes Survey

    CONTROL CONSOLE FOR MTR FISSION PRODUCT MONITOR, USED TO DETECT BREAKS IN CLADDING OF FUEL ELEMENTS. COUNT-RATE METER IN TOP PANEL INDICATES AMOUNT OF RADIOACTIVITY. LOWER PANELS SUPPLY POWER AND AMPLIFICATION OF SIGNALS GENERATED BY SCINTILLATION COUNTER/PHOTOMULTIPLIER TUBE COMBINATION IN RESPONSE TO RADIOACTIVITY IN A SAMPLE OF THE COOLING WATER. INL NEGATIVE NO. 56-771. Jack L. Anderson, Photographer, 3/15/1956. - Idaho National Engineering Laboratory, Test Reactor Area, Materials & Engineering Test Reactors, Scoville, Butte County, ID

  4. Simulations of the fission-product stopping efficiency in IGISOL

    NASA Astrophysics Data System (ADS)

    Al-Adili, A.; Jansson, K.; Lantz, M.; Solders, A.; Gorelov, D.; Gustavsson, C.; Mattera, A.; Moore, I.; Prokofiev, A. V.; Rakopoulos, V.; Penttilä, H.; Tarrío, D.; Wiberg, S.; Österlund, M.; Pomp, S.

    2015-05-01

    At the Jyväskylä Ion Guide Isotope Separator On-Line (IGISOL) facility, independent fission yields are measured employing the Penning-trap technique. Fission products are produced, e.g. by impinging protons on a uranium target, and are stopped in a gas-filled chamber. The products are collected by a flow of He gas and guided through a mass separator to a Penning trap, where their masses are identified. This work investigates how fission-product properties, such as mass and energy, affect the ion stopping efficiency in the gas cell. The study was performed using the Geant4 toolkit and the SRIM code. The main results show a nearly mass-independent ion stopping with regard to the wide spread of ion masses and energies, with a proper choice of uranium target thickness. Although small variations were observed, in the order of 5%, the results are within the systematic uncertainties of the simulations. To optimize the stopping efficiency while reducing the systematic errors, different experimental parameters were varied; for instance material thicknesses and He gas pressure. Different parameters influence the mass dependence and could alter the mass dependencies in the ion stopping efficiency.

  5. Rapid separation of individual lanthanide elements from mixed fission products

    SciTech Connect

    Baker, J.D.

    1980-11-01

    A microprocessor-controlled radiochemical separation system has been developed to separate lanthanide elements rapidly from fission products. The system is composed of two high performance liquid chromatography columns coupled in series by a stream-splitting injection valve. The first column separates the lanthanide group by extraction-chromatography using dihexyldiethylcarbamylmethyleneophoshate (DHDECMP) adsorbed on Vydac C/sub 8/ resin. The second column isolates the individual lanthanide elements by cation exchange using Aminex A-9 resin with ..cap alpha..-hydroxyisobutyric acid (..cap alpha..-HIBA) as the eluent. With this system, the fission-product lanthanide isotope /sup 158/Sm has been identified for the first time. It was produced from a spontaneously fissioning /sup 252/Cf source. Twenty-seven gamma-rays have been assigned to this activity which decays with a half-life of 5.51 +- 0.09 min. The /sup 158/Sm assignment is based upon the radiochemical separation of the Sm fraction from the lanthanide fission products and the observation of the growth and decay of the 45.9 min /sup 158/Eu daughter from an initially pure 5 min parent. The emission probability of the 324-keV gamma ray of /sup 158/Sm was also determined, from the growth and decay of the /sup 158/Eu daughter, to be 10.6 +- 1.2 gamma rays per 100 decays. Several new gamma rays have been identified by half-life as belonging to the decay of /sup 157/Sm. Gamma-ray energies and relative intensities for /sup 157/Sm and /sup 158/Sm are reported.

  6. RAPID QUANTITATION OF URANIUM FROM MIXED FISSION PRODUCT SAMPLES

    SciTech Connect

    Haney, Morgan M.; Seiner, Brienne N.; Finn, Erin C.; Friese, Judah I.

    2016-03-09

    Chemical similarities between U(VI) and Mo(VI) create challenges for separation and quantification of uranium from a mixed fission product sample. The purpose of this work was to demonstrate the feasibility of using Eichrom’s® UTEVA resin in addition to a tellurium spontaneous deposition to improve the quantitation of 235U using gamma spectroscopy. The optimized method demonstrated a consistent chemical yield of 74 ± 3 % for uranium. This procedure was evaluated using 1.41x1012 fissions produced from an irradiated HEU sample. The uranium was isotopically yielded by HPGe, and the minimum detectable activity (MDA) determined from the gamma spectra. The MDA for 235U, 237U, and 238U was reduced by a factor of two. The chemical isolation of uranium was successfully achieved in less than four hours, with a separation factor of 1.41x105 from molybdenum.

  7. Venting of fission products and shielding in thermionic nuclear reactor systems

    NASA Technical Reports Server (NTRS)

    Salmi, E. W.

    1972-01-01

    Most thermionic reactors are designed to allow the fission gases to escape out of the emitter. A scheme to allow the fission gases to escape is proposed. Because of the low activity of the fission products, this method should pose no radiation hazards.

  8. Evaluation of Cross-Section Sensitivities in Computing Burnup Credit Fission Product Concentrations

    SciTech Connect

    Gauld, I.C.

    2005-08-12

    U.S. Nuclear Regulatory Commission Interim Staff Guidance 8 (ISG-8) for burnup credit covers actinides only, a position based primarily on the lack of definitive critical experiments and adequate radiochemical assay data that can be used to quantify the uncertainty associated with fission product credit. The accuracy of fission product neutron cross sections is paramount to the accuracy of criticality analyses that credit fission products in two respects: (1) the microscopic cross sections determine the reactivity worth of the fission products in spent fuel and (2) the cross sections determine the reaction rates during irradiation and thus influence the accuracy of predicted final concentrations of the fission products in the spent fuel. This report evaluates and quantifies the importance of the fission product cross sections in predicting concentrations of fission products proposed for use in burnup credit. The study includes an assessment of the major fission products in burnup credit and their production precursors. Finally, the cross-section importances, or sensitivities, are combined with the importance of each major fission product to the system eigenvalue (k{sub eff}) to determine the net importance of cross sections to k{sub eff}. The importances established the following fission products, listed in descending order of priority, that are most likely to benefit burnup credit when their cross-section uncertainties are reduced: {sup 151}Sm, {sup 103}Rh, {sup 155}Eu, {sup 150}Sm, {sup 152}Sm, {sup 153}Eu, {sup 154}Eu, and {sup 143}Nd.

  9. Methods to Collect, Compile, and Analyze Observed Short-lived Fission Product Gamma Data

    SciTech Connect

    Finn, Erin C.; Metz, Lori A.; Payne, Rosara F.; Friese, Judah I.; Greenwood, Lawrence R.; Kephart, Jeremy D.; Pierson, Bruce D.; Ellis, Tere A.

    2011-09-29

    A unique set of fission product gamma spectra was collected at short times (4 minutes to 1 week) on various fissionable materials. Gamma spectra were collected from the neutron-induced fission of uranium, neptunium, and plutonium isotopes at thermal, epithermal, fission spectrum, and 14-MeV neutron energies. This report describes the experimental methods used to produce and collect the gamma data, defines the experimental parameters for each method, and demonstrates the consistency of the measurements.

  10. Insights on fission products behaviour in nuclear severe accident conditions by X-ray absorption spectroscopy

    NASA Astrophysics Data System (ADS)

    Geiger, E.; Bès, R.; Martin, Ph; Pontillon, Y.; Ducros, G.; Solari, P. L.

    2016-04-01

    Many research programs have been carried out aiming to understand the fission products behaviour during a Nuclear Severe Accident. Most of these programs used highly radioactive irradiated nuclear fuel, which requires complex instrumentation. Moreover, the radioactive character of samples hinders an accurate chemical characterisation. In order to overcome these difficulties, SIMFUEL stand out as an alternative to perform complementary tests. A sample made of UO2 doped with 11 fission products was submitted to an annealing test up to 1973 K in reducing atmosphere. The sample was characterized before and after the annealing test using SEM-EDS and XAS at the MARS beam-line, SOLEIL Synchrotron. It was found that the overall behaviour of several fission products (such as Mo, Ba, Pd and Ru) was similar to that observed experimentally in irradiated fuels and consistent with thermodynamic estimations. The experimental approach presented in this work has allowed obtaining information on chemical phases evolution under nuclear severe accident conditions, that are yet difficult to obtain using irradiated nuclear fuel samples.

  11. Linear free energy correlations for fission product release from the Fukushima-Daiichi nuclear accident.

    PubMed

    Abrecht, David G; Schwantes, Jon M

    2015-03-03

    This paper extends the preliminary linear free energy correlations for radionuclide release performed by Schwantes et al., following the Fukushima-Daiichi Nuclear Power Plant accident. Through evaluations of the molar fractionations of radionuclides deposited in the soil relative to modeled radionuclide inventories, we confirm the initial source of the radionuclides to the environment to be from active reactors rather than the spent fuel pool. Linear correlations of the form In χ = −α ((ΔGrxn°(TC))/(RTC)) + β were obtained between the deposited concentrations, and the reduction potentials of the fission product oxide species using multiple reduction schemes to calculate ΔG°rxn (TC). These models allowed an estimate of the upper bound for the reactor temperatures of TC between 2015 and 2060 K, providing insight into the limiting factors to vaporization and release of fission products during the reactor accident. Estimates of the release of medium-lived fission products 90Sr, 121mSn, 147Pm, 144Ce, 152Eu, 154Eu, 155Eu, and 151Sm through atmospheric venting during the first month following the accident were obtained, indicating that large quantities of 90Sr and radioactive lanthanides were likely to remain in the damaged reactor cores.

  12. Linear Free Energy Correlations for Fission Product Release from the Fukushima-Daiichi Nuclear Accident

    SciTech Connect

    Abrecht, David G.; Schwantes, Jon M.

    2015-03-03

    This paper extends the preliminary linear free energy correlations for radionuclide release performed by Schwantes, et al., following the Fukushima-Daiichi Nuclear Power Plant accident. Through evaluations of the molar fractionations of radionuclides deposited in the soil relative to modeled radionuclide inventories, we confirm the source of the radionuclides to be from active reactors rather than the spent fuel pool. Linear correlations of the form ln χ = -α (ΔGrxn°(TC))/(RTC)+β were obtained between the deposited concentration and the reduction potential of the fission product oxide species using multiple reduction schemes to calculate ΔG°rxn(TC). These models allowed an estimate of the upper bound for the reactor temperatures of TC between 2130 K and 2220 K, providing insight into the limiting factors to vaporization and release of fission products during the reactor accident. Estimates of the release of medium-lived fission products 90Sr, 121mSn, 147Pm, 144Ce, 152Eu, 154Eu, 155Eu, 151Sm through atmospheric venting and releases during the first month following the accident were performed, and indicate large quantities of 90Sr and radioactive lanthanides were likely to remain in the damaged reactor cores.

  13. Accelerator-Driven Production of Fission 99Mo

    SciTech Connect

    Youker, A. J.; Chemerisov, S. D.; Tkac, P.; Krebs, J. F.; Rotsch, D. A.; Kalensky, M.; Heltemes, T. A.; Alford, K.; Byrnes, J. P.; Gromov, R.; Hafenrichter, L.; Hebden, A. S.; Jerden, J. L.; Jonah, C. D.; Makarashvili, V.; Quigley, K. J.; Schneider, J. F.; Stepinski, D. C.; Wesolowski, K. A.; Vandegrift, G. F.

    2016-01-01

    I{esults al'e reportecl for the procluction of eeMo l'rom the accelerator-clriveu subcritical fission of a low enriohed uranir¡m (Ltju) aqì.reous solution. Phase I ol'these experiments used a 5 L r.rranyl sulfate solution with a eeMo encl-of-irracliation produotion limit of 2 Ci. The separation, recovery, and pulification of eeMo were demonstrated Lrsing the recyclecl solution. Fission product paltitioriing tl'ends will be shown for the recovery colutt'ttt, concentratiorl colurnn, and LE,U Modified Cintichem prooess. The results fi'om a 1.4 Ci oeMo production run, where the fìnal product was seut to GE Flealthcare for testing, will be highlightecl. The information gained cluring Phase ì lias signilìcantly irnpacted the clesign and implernentation of Phase ll. Phase II focuses on an end-of-irradiation ploduction of 20 Ci of eeMo and a fissior'ì power density similar to the production fàcility in a20 L LìlU uranyl sulfate solution.

  14. Fission product yield evaluation for the USA evaluated nuclear data files

    SciTech Connect

    Rider, B.F.; England, T.R.

    1994-10-01

    An evaluated set of fission product yields for use in calculation of decay heat curves with improved accuracy has been prepared. These evaluated yields are based on all known experimental data through 1992. Unmeasured fission product yields are calculated from charge distribution, pairing effects, and isomeric state models developed at Los Alamos National Laboratory. The current evaluation has been distributed as the ENDF/B-VI fission product yield data set.

  15. Migration of fission products in UO{sub 2}. Final report

    SciTech Connect

    Prussin, S.G.; Olander, D.R.

    1995-12-01

    Results of an experimental and calculational effort to examine the fundamental mechanisms of fission product migration in and release from polycrystalline uranium dioxide are reported. The experiments were designed to provide diffusion parameters for the representative fission products tellurium, iodine, xenon, molybdenum and ruthenium under both reducing and oxidizing conditions. The calculational effort applied a new model of fission product release from reactor fuel that incorporates grain growth as well as grain boundary and lattice diffusion.

  16. PURIFICATION OF PLUTONIUM USING A CERIUM PRECIPITATE AS A CARRIER FOR FISSION PRODUCTS

    DOEpatents

    Faris, B.F.; Olson, C.M.

    1961-07-01

    Bismuth phosphate carrier precipitation processes are described for the separation of plutonium from fission products wherein in at least one step bismuth phosphate is precipitated in the presence of hexavalent plutonium thereby carrying a portion of the fission products from soluble plu tonium values. In this step, a cerium phosphate precipitate is formed in conjunction with the bismuth phosphate precipitate, thereby increasing the amount of fission products removed from solution.

  17. Equilibrium Temperature Profiles within Fission Product Waste Forms

    SciTech Connect

    Kaminski, Michael D.

    2016-10-01

    We studied waste form strategies for advanced fuel cycle schemes. Several options were considered for three waste streams with the following fission products: cesium and strontium, transition metals, and lanthanides. These three waste streams may be combined or disposed separately. The decay of several isotopes will generate heat that must be accommodated by the waste form, and this heat will affect the waste loadings. To help make an informed decision on the best option, we present computational data on the equilibrium temperature of glass waste forms containing a combination of these three streams.

  18. Methodology and application of the WIMS-D4M fission product data

    SciTech Connect

    Mo, S.C.

    1995-02-01

    The WIMS-D4 code has been modified (WIMS-D4m) to generate burn-up dependent microscopic cross sections for use in full core depletion calculations. The calculation of neutron absorption by fission products can be obtained from a reduced fission-product-chain model that includes the {sup 135}Xe and {sup 149}Sm chains, and a lumped fission product to account for the absorption by fission products not explicitly treated. Burn-up calculations were performed for the ANS MEU core using WIMS and EPRI-CELL cross sections. The calculated eigenvalues and material loadings are in good agreements.

  19. Assessment of selected fission products in the Savannah River Site environment

    SciTech Connect

    Carlton, W.H.; Denham, M.

    1997-04-01

    Most of the radioactivity produced by the operation of a nuclear reactor results from the fission process, during which the nucleus of a fissionable atom (such as 235U) splits into two or more nuclei, which typically are radioactive. The Radionuclide Assessment Program (RAP) has reported on fission products cesium, strontium, iodine, and technetium. Many other radionuclides are produced by the fission process. Releases of several additional fission products that result in dose to the offsite population are discussed in this publication. They are 95Zr, 95Nb, 103Ru, 106Ru, 141Ce, and 144Ce. This document will discuss the production, release, migration, and dose to humans for each of these selected fission products.

  20. A proposed standard on medical isotope production in fission reactors

    SciTech Connect

    Schenter, R. E.; Brown, G. J.; Holden, C. S.

    2006-07-01

    Authors Robert E. Sehenter, Garry Brown and Charles S. Holden argue that a Standard for 'Medical Isotope Production' is needed. Medical isotopes are becoming major components of application for the diagnosis and treatment of all the major diseases including all forms of cancer, heart disease, arthritis, Alzheimer's, among others. Current nuclear data to perform calculations is incomplete, dated or imprecise or otherwise flawed for many isotopes that could have significant applications in medicine. Improved data files will assist computational analyses to design means and methods for improved isotope production techniques in the fission reactor systems. Initial focus of the Standard is expected to be on neutron cross section and branching data for both fast and thermal reactor systems. Evaluated and reviewed tables giving thermal capture cross sections and resonance integrals for the major target and product medical isotopes would be the expected 'first start' for the 'Standard Working Group'. (authors)

  1. Biological removal of cationic fission products from nuclear wastewater.

    PubMed

    Ngwenya, N; Chirwa, E M N

    2011-01-01

    Nuclear energy is becoming a preferred energy source amidst rising concerns over the impacts of fossil fuel based energy on global warming and climate change. However, the radioactive waste generated during nuclear power generation contains harmful long-lived fission products such as strontium (Sr). In this study, cationic strontium uptake from solution by microbial cultures obtained from mine wastewater is evaluated. A high strontium removal capacity (q(max)) with maximum loading of 444 mg/g biomass was achieved by a mixed sulphate reducing bacteria (SRB) culture. Sr removal in SRB was facilitated by cell surface based electrostatic interactions with the formation of weak ionic bonds, as 68% of the adsorbed Sr(2+) was easily desorbed from the biomass in an ion exchange reaction with MgCl₂. To a lesser extent, precipitation reactions were also found to account for the removal of Sr from aqueous solution as about 3% of the sorbed Sr was precipitated due to the presence of chemical ligands while the remainder occurred as an immobile fraction. Further analysis of the Sr-loaded SRB biomass by scanning electron microscopy (SEM) coupled to energy dispersive X-ray (EDX) confirmed extracellular Sr(2+) precipitation as a result of chemical interaction. In summary, the obtained results demonstrate the prospects of using biological technologies for the remediation of industrial wastewaters contaminated by fission products.

  2. Immobilization of fission products in phosphate ceramic waste forms

    SciTech Connect

    Singh, D.; Wagh, A.

    1997-10-01

    Chemically bonded phosphate ceramics (CBPCs) have several advantages that make them ideal candidates for containing radioactive and hazardous wastes. In general, phosphates have high solid-solution capacities for incorporating radionuclides, as evidenced by several phosphates (e.g., monazites and apatites) that are natural analogs of radioactive and rare-earth elements. The phosphates have high radiation stability, are refractory, and will not degrade in the presence of internal heating by fission products. Dense and hard CBPCs can be fabricated inexpensively and at low temperature by acid-base reactions between an inorganic oxide/hydroxide powder and either phosphoric acid or an acid-phosphate solution. The resulting phosphates are extremely insoluble in aqueous media and have excellent long-term durability. CBPCs offer the dual stabilization mechanisms of chemical fixation and physical encapsulation, resulting in superior waste forms. The goal of this task is develop and demonstrate the feasibility of CBPCs for S/S of wastes containing fission products. The focus of this work is to develop a low-temperature CBPC immobilization system for eluted {sup 99}Tc wastes from sorption processes.

  3. Preliminary investigation of a technique to separate fission noble metals from fission product mixtures

    SciTech Connect

    Mellinger, G.B.; Jensen, G.A.

    1982-08-01

    A variation of the gold-ore fire assay technique was examined as a method for recovering Pd, Rh and Ru from fission products. The mixture of fission product oxides is combined with glass-forming chemicals, a metal oxide such as PbO (scavenging agent), and a reducing agent such as charcoal. When this mixture is melted, a metal button is formed which extracts the noble metals. The remainder cools to form a glass for nuclear waste storage. Recovery depended only on reduction of the scavenger oxide to metal. When such reduction was achieved, no difference in noble metal recovery efficiency was found among the scavengers studied (PbO, SnO, CuO, Bi/sub 2/O/sub 3/, Sb/sub 2/O/sub 3/). Not all reducing agents studied, however, were able to reduce all scavenger oxides to metal. Only graphite would reduce SnO and CuO and allow noble metal recovery. The scavenger oxides Sb/sub 2/O/sub 3/, Bi/sub 2/O/sub 3/, and PbO, however, were reduced by all of the reducing agents tested. Similar noble metal recovery was found with each. Lead oxide was found to be the most promising of the potential scavengers. It was reduced by all of the reducing agents tested, and its higher density may facilitate the separation. Use of lead oxide also appeared to have no deterimental effect on the glass quality. Charcoal was identified as the preferred reducing agent. As long as a separable metal phase was formed in the melt, noble metal recovery was not dependent on the amount of reducing agent and scavenger oxide. High glass viscosities inhibited separation of the molten scavenger, while low viscosities allowed volatile loss of RuO/sub 4/. A viscosity of approx. 20 poise at the processing temperature offered a good compromise between scavenger separation and Ru recovery. Glasses in which PbO was used as the scavenging agent were homogeneous in appearance. Resistance to leaching was close to that of certain waste glasses reported in the literature. 12 figures. 7 tables.

  4. Experimental Measurements of Short-Lived Fission Products from Uranium, Neptunium, Plutonium and Americium

    SciTech Connect

    Metz, Lori A.; Payne, Rosara F.; Friese, Judah I.; Greenwood, Lawrence R.; Kephart, Jeremy D.; Pierson, Bruce D.

    2009-11-01

    Fission yields are especially well characterized for long-lived fission products. Modeling techniques incorporate numerous assumptions and can be used to deduce information about the distribution of short-lived fission products. This work is an attempt to gather experimental (model-independent) data on the short-lived fission products. Fissile isotopes of uranium, neptunium, plutonium and americium were irradiated under pulse conditions at the Washington State University 1 MW TRIGA reactor to achieve ~108 fissions. The samples were placed on a HPGe (high purity germanium) detector to begin counting in less than 3 minutes post irradiation. The samples were counted for various time intervals ranging from 5 minutes to 1 hour. The data was then analyzed to determine which radionuclides could be quantified and compared to the published fission yield data.

  5. Fission products of superheavy elements. An investigation of the naturally occurring fission products of elements heavier than uranium

    NASA Technical Reports Server (NTRS)

    Marti, K.

    1972-01-01

    Fission mass yields in different structural elements and mineral separates were studied for the element X. The fission component for Pu-244, and the element X are discussed along with radiogenic Xe-129 and neutron activitation.

  6. Fission Product Yields from Fission Spectrum n+{sup 239}Pu for ENDF/B-VII.1

    SciTech Connect

    Chadwick, M.B.; Kawano, T.; Barr, D.W.; Mac Innes, M.R.; Kahler, A.C.; Graves, T.; Selby, H.; Burns, C.J.; Inkret, W.C.; Keksis, A.L.; Lestone, J.P.; Sierk, A.J.; Talou, P.

    2010-12-15

    We describe a new cumulated fission product yield (FPY) evaluation for fission spectrum neutrons on plutonium that updates the ENDF/B-VI evaluation by England and Rider, for the forthcoming ENDF/B-VII.1 database release. We focus on FPs that are needed for high accuracy burnup assessments; that is, for inferring the number of fissions in a neutron environment. Los Alamos conducted an experiment in the 1970s in the Bigten fast critical assembly to determine fission product yields as part of the Interlaboratory Reaction Rate (ILRR) collaboration, and this has defined the Laboratory's fission standard to this day. Our evaluation includes use of the LANL-ILRR measurements (not previously available to evaluators) as well as other Laboratory FPY measurements published in the literature, especially the high-accuracy mass spectrometry data from Maeck and others. Because the measurement database for some of the FPs is small - especially for {sup 99}Mo - we use a meta-analysis that incorporates insights from other accurately-measured benchmark FP data, using R-value ratio measurements. The meta-analysis supports the FP measurements from the LANL-ILRR experiment. Differences between our new evaluations and ENDF/B-VI are small for some FPs (less than 1-2%-relative for {sup 95}Zr, {sup 140}Ba, {sup 144}Ce), but are larger for {sup 99}Mo (4%-relative) and {sup 147}Nd (5%-relative, at 1.5 MeV) respectively. We present evidence for an incident neutron energy dependence to the {sup 147}Nd fission product yield that accounts for observed differences in the FPY at a few-hundred keV average energy in fast reactors versus measurements made at higher average neutron energies in Los Alamos' fast critical assemblies. Accounting for such FPY neutron energy dependencies is important if one wants to reach a goal of determining the number of fissions to accuracies of 1-2%. An evaluation of the energy-dependence of fission product yields is given for all A values based on systematical trends

  7. Assessment of fission product yields data needs in nuclear reactor applications

    SciTech Connect

    Kern, K.; Becker, M.; Broeders, C.

    2012-07-01

    Studies on the build-up of fission products in fast reactors have been performed, with particular emphasis on the effects related to the physics of the nuclear fission process. Fission product yields, which are required for burn-up calculations, depend on the proton and neutron number of the target nucleus as well as on the incident neutron energy. Evaluated nuclear data on fission product yields are available for all relevant target nuclides in reactor applications. However, the description of their energy dependence in evaluated data is still rather rudimentary, which is due to the lack of experimental fast fission data and reliable physical models. Additionally, physics studies of evaluated JEFF-3.1.1 fission yields data have shown potential improvements, especially for various fast fission data sets of this evaluation. In recent years, important progress in the understanding of the fission process has been made, and advanced model codes are currently being developed. This paper deals with the semi-empirical approach to the description of the fission process, which is used in the GEF code being developed by K.-H. Schmidt and B. Jurado on behalf of the OECD Nuclear Energy Agency, and with results from the corresponding author's diploma thesis. An extended version of the GEF code, supporting the calculation of spectrum weighted fission product yields, has been developed. It has been applied to the calculation of fission product yields in the fission rate spectra of a MOX fuelled sodium-cooled fast reactor. Important results are compared to JEFF-3.1.1 data and discussed in this paper. (authors)

  8. SEPARATION OF URANIUM, PLUTONIUM AND FISSION PRODUCTS FROM NEUTRON- BOMBARDED URANIUM

    DOEpatents

    Martin, A.E.; Johnson, I.; Burris, L. Jr.; Winsch, I.O.; Feder, H.M.

    1962-11-13

    A process is given for removing plutonium and/or fission products from uranium fuel. The fuel is dissolved in molten zinc--magnesium (10 to 18% Mg) alloy, more magnesium is added to obtain eutectic composition whereby uranium precipitates, and the uranium are separated from the Plutoniumand fission-product- containing eutectic. (AEC)

  9. Analysis of Fission Products on the AGR-1 Capsule Components

    SciTech Connect

    Paul A. Demkowicz; Jason M. Harp; Philip L. Winston; Scott A. Ploger

    2013-03-01

    The components of the AGR-1 irradiation capsules were analyzed to determine the retained inventory of fission products in order to determine the extent of in-pile fission product release from the fuel compacts. This includes analysis of (i) the metal capsule components, (ii) the graphite fuel holders, (iii) the graphite spacers, and (iv) the gas exit lines. The fission products most prevalent in the components were Ag-110m, Cs 134, Cs 137, Eu-154, and Sr 90, and the most common location was the metal capsule components and the graphite fuel holders. Gamma scanning of the graphite fuel holders was also performed to determine spatial distribution of Ag-110m and radiocesium. Silver was released from the fuel components in significant fractions. The total Ag-110m inventory found in the capsules ranged from 1.2×10 2 (Capsule 3) to 3.8×10 1 (Capsule 6). Ag-110m was not distributed evenly in the graphite fuel holders, but tended to concentrate at the axial ends of the graphite holders in Capsules 1 and 6 (located at the top and bottom of the test train) and near the axial center in Capsules 2, 3, and 5 (in the center of the test train). The Ag-110m further tended to be concentrated around fuel stacks 1 and 3, the two stacks facing the ATR reactor core and location of higher burnup, neutron fluence, and temperatures compared with Stack 2. Detailed correlation of silver release with fuel type and irradiation temperatures is problematic at the capsule level due to the large range of temperatures experienced by individual fuel compacts in each capsule. A comprehensive Ag 110m mass balance for the capsules was performed using measured inventories of individual compacts and the inventory on the capsule components. For most capsules, the mass balance was within 11% of the predicted inventory. The Ag-110m release from individual compacts often exhibited a very large range within a particular capsule.

  10. Exploratory study of fission product yields of neutron-induced fission of U235, U238, and Pu239 at 8.9 MeV

    DOE PAGES

    Bhatia, C.; Fallin, B. F.; Gooden, M. E.; ...

    2015-06-05

    Using dual-fission chambers each loaded with a thick (200–400–mg/cm2) actinide target of 235,238U or 239Pu and two thin (~10–100–μg/cm2) reference foils of the same actinide, the cumulative yields of fission products ranging from 92Sr to 147Nd have been measured at En = 8.9MeV. The 2H(d,n) 3He reaction provided the quasimonoenergetic neutron beam. Here, the experimental setup and methods used to determine the fission product yield (FPY) are described, and results for typically eight high-yield fission products are presented.

  11. Target and method for the production of fission product molybdenum-99

    DOEpatents

    Vandegrift, G.F.; Vissers, D.R.; Marshall, S.L.; Varma, R.

    1987-10-26

    A target for the reduction of fission product Mo-99 is prepared from uranium of low U-235 enrichment by coating a structural support member with a preparatory coating of a substantially oxide-free substrate metal. Uranium metal is electrodeposited from a molten halide electrolytic bath onto a substrate metal. The electrodeposition is performed at a predetermined direct current rate or by using pulsed plating techniques which permit relaxation of accumulated uranium ion concentrations within the melt. Layers of as much as to 600 mg/cm/sup 2/ of uranium can be prepared to provide a sufficient density to produce acceptable concentrations of fission product Mo-99. 2 figs.

  12. Target and method for the production of fission product molybdenum-99

    DOEpatents

    Vandegrift, George F.; Vissers, Donald R.; Marshall, Simon L.; Varma, Ravi

    1989-01-01

    A target for the reduction of fission product Mo-99 is prepared from uranium of low U-235 enrichment by coating a structural support member with a preparatory coating of a substantially oxide-free substrate metal. Uranium metal is electrodeposited from a molten halide electrolytic bath onto a substrate metal. The electrodeposition is performed at a predetermined direct current rate or by using pulsed plating techniques which permit relaxation of accumulated uranium ion concentrations within the melt. Layers of as much as to 600 mg/cm.sup.2 of uranium can be prepared to provide a sufficient density to produce acceptable concentrations of fission product Mo-99.

  13. SEPARATION OF PLUTONIUM VALUES FROM URANIUM AND FISSION PRODUCT VALUES

    DOEpatents

    Maddock, A.G.; Booth, A.H.

    1960-09-13

    Separation of plutonium present in small amounts from neutron irradiated uranium by making use of the phenomenon of chemisorption is described. Plutonium in the tetravalent state is chemically absorbed on a fluoride in solid form. The steps for the separation comprise dissolving the irradiated uranium in nitric acid, oxidizing the plutonium in the resulting solution to the hexavalent state, adding to the solution a soluble calcium salt which by the common ion effect inhibits dissolution of the fluoride by the solution, passing the solution through a bed or column of subdivided calcium fluoride which has been sintered to about 8OO deg C to remove the chemisorbable fission products, reducing the plutonium in the solution thus obtained to the tetravalent state, and again passing the solution through a similar bed or column of calcium fluoride to selectively absorb the plutonium, which may then be recovered by treating the calcium fluoride with a solution of ammonium oxalate.

  14. ZIRCONIUM AND FISSION PRODUCT MANAGEMENT IN THE ALSEP PROCESS

    SciTech Connect

    Lumetta, Gregg J.; Carter, Jennifer C.; Niver, Cynthia M.; Gelis, Artem V.

    2013-09-29

    Solvent extraction systems that combine neutral donor extractants and acidic extractants are being investigated to provide a single process solvent for separating Am and Cm from acidic high-level liquid waste, including their separation from the trivalent lanthanides. This approach of combining extractants is collectively referred to as the Actinide-Lanthanide SEParation (ALSEP) process. Managing Zr and other fission products is one of the critical factors in developing the ALSEP process. In this work, a strategy has been developed in which Zr(IV) is extracted into the process solvent, then it is stripped from the solvent after the actinides have been selectively stripped. Molybdenum is strongly extracted into ALSEP solvents. Scrubbing the solvent with a citrate buffer before the actinide stripping step effectively removes Mo. Distribution ratios for Ru and Fe are low for extraction from HNO3, so these components can easily be routed to the high-level waste raffinate.

  15. Neutron Cross Section Covariances for Structural Materials and Fission Products

    NASA Astrophysics Data System (ADS)

    Hoblit, S.; Cho, Y.-S.; Herman, M.; Mattoon, C. M.; Mughabghab, S. F.; Obložinský, P.; Pigni, M. T.; Sonzogni, A. A.

    2011-12-01

    We describe neutron cross section covariances for 78 structural materials and fission products produced for the new US evaluated nuclear reaction library ENDF/B-VII.1. Neutron incident energies cover full range from 10 eV to 20 MeV and covariances are primarily provided for capture, elastic and inelastic scattering as well as (n,2n). The list of materials follows priorities defined by the Advanced Fuel Cycle Initiative, the major application being data adjustment for advanced fast reactor systems. Thus, in addition to 28 structural materials and 49 fission products, the list includes also 23Na which is important fast reactor coolant. Due to extensive amount of materials, we adopted a variety of methodologies depending on the priority of a specific material. In the resolved resonance region we primarily used resonance parameter uncertainties given in Atlas of Neutron Resonances and either applied the kernel approximation to propagate these uncertainties into cross section uncertainties or resorted to simplified estimates based on integral quantities. For several priority materials we adopted MF32 covariances produced by SAMMY at ORNL, modified by us by adding MF33 covariances to account for systematic uncertainties. In the fast neutron region we resorted to three methods. The most sophisticated was EMPIRE-KALMAN method which combines experimental data from EXFOR library with nuclear reaction modeling and least-squares fitting. The two other methods used simplified estimates, either based on the propagation of nuclear reaction model parameter uncertainties or on a dispersion analysis of central cross section values in recent evaluated data files. All covariances were subject to quality assurance procedures adopted recently by CSEWG. In addition, tools were developed to allow inspection of processed covariances and computed integral quantities, and for comparing these values to data from the Atlas and the astrophysics database KADoNiS.

  16. Measurement of fission products yields in the quasi-mono-energetic neutron-induced fission of 232Th

    NASA Astrophysics Data System (ADS)

    Naik, H.; Mukherji, Sadhana; Suryanarayana, S. V.; Jagadeesan, K. C.; Thakare, S. V.; Sharma, S. C.

    2016-08-01

    The cumulative yields of various fission products in the 232Th(n, f) reaction at average neutron energies of 5.42, 7.75, 9.35 and 12.53 MeV have been determined by using an off-line γ-ray spectrometric technique. The neutron beam was produced from the 7Li(p, n) reaction by using the proton energies of 7.8, 12, 16 and 20 MeV. The mass chain yields were obtained from the cumulative fission yields by using the charge distribution correction of medium energy fission. The fine structure in the mass yield distribution was interpreted from the point of nuclear structure effect. On the other hand, the higher yield around mass number 133-134 and 143-144 as well as their complementary products were explained based on the standard I and standard II asymmetric mode of fission. From the mass yield data, the average value of light mass (), heavy mass (), the average number of neutrons (< ν >) and the peak-to-valley (P / V) ratios at different neutron energies of present work and literature data were obtained in the 232Th(n, f) reaction. The different parameters of the mass yield distribution in the 232Th(n, f) reaction were compared with the similar data in the 232Th(γ, f) reaction at comparable excitation energy and a surprising difference was observed.

  17. Investigation of the Fission Product Release From Molten Pools Under Oxidizing Conditions With the Code RELOS

    SciTech Connect

    Kleinhietpass, Ingo D.; Unger, Hermann; Wagner, Hermann-Josef; Koch, Marco K.

    2006-07-01

    With the purpose of modeling and calculating the core behavior during severe accidents in nuclear power plants system codes are under development worldwide. Modeling of radionuclide release and transport in the case of beyond design basis accidents is an integrated feature of the deterministic safety analysis of nuclear power plants. Following a hypothetical, uncontrolled temperature escalation in the core of light water reactors, significant parts of the core structures may degrade and melt down under formation of molten pools, leading to an accumulation of large amounts of radioactive materials. The possible release of radionuclides from the molten pool provides a potential contribution to the aerosol source term in the late phase of core degradation accidents. The relevance of the amount of transferred oxygen from the gas atmosphere into the molten pool on the specification of a radionuclide and its release depends strongly on the initial oxygen inventory. Particularly for a low oxygen potential in the melt as it is the case for stratification when a metallic phase forms the upper layer and, respectively, when the oxidation has proceeded so far so that zirconium was completely oxidized, a significant influence of atmospheric oxygen on the specification and the release of some radionuclides has to be anticipated. The code RELOS (Release of Low Volatile Fission Products from Molten Surfaces) is under development at the Department of Energy Systems and Energy Economics (formerly Department of Nuclear and New Energy Systems) of the Ruhr-University Bochum. It is based on a mechanistic model to describe the diffusive and convective transport of fission products from the surface of a molten pool into a cooler gas atmosphere. This paper presents the code RELOS, i. e. the features and abilities of the latest code version V2.3 and the new model improvements of V2.4 and the calculated results evaluating the implemented models which deal with the oxygen transfer from the

  18. 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

    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

  19. Europa's Atmosphere: Production & Loss

    NASA Astrophysics Data System (ADS)

    Bagenal, F.; Cassidy, T. A.; Dols, V.; Crary, F. J.

    2013-12-01

    Europa is embedded not only in the ionized material of the Io plasma torus, but is also surrounded by the material (both ionized and neutral) produced by the interaction of this plasma with the moon's surface and atmosphere. Moreover, there are energetic ions and electrons that diffuse inwards from the outer magnetosphere and interact with the moon and surrounding neutral clouds. The multiple components of Europa's environment are thought to vary on timescales of hours to weeks and to be strongly coupled. Europa's O2 atmosphere is created by ion bombardment of the surface. Earlier studies assumed that the energetic (10s keV) ions were responsible (see review in Smyth and Marconi, 2006). New research (Cassidy et al. 2013) suggests that the 'thermal' ion population of the Io plasma torus produces most of Europa's O2. But this cooler population is easily diverted by currents induced in Europa's ionosphere and prevented from reaching the surface. This feedback has not been adequately explored. Modelers have historically focused on a single piece of the puzzle; plasma modelers assume a static atmosphere and atmosphere modelers assume static plasma. We are now in a position to consider these new sources of atmosphere and determine how the observed system comes about as well as quantify the timescales and causes of its evolution. This begs the question is Europa's atmosphere-magnetosphere interaction self-regulating? We are specifically interested in how the system responds to changes - for example, how does Europa's atmosphere change when the inflowing plasma flux increases or decreases? What is the corresponding change in the electrodynamics and diversion of plasma flow around Europa? How much and on what time scale does the extended neutral cloud respond? And what are the consequences for the influx of energetic particles? We model this coupled system to address how each component responds to changes in the other components.

  20. Short-lived fission product measurements from >0.1 MeV neutron-induced fission using boron carbide.

    SciTech Connect

    Finn, Erin C.; Metz, Lori A.; Greenwood, Lawrence R.; Pierson, Bruce D.; Friese, Judah I.; Kephart, Rosara F.; Kephart, Jeremy D.

    2012-02-01

    A boron carbide shield was designed, custom fabricated, and used to create a fast fission energy neutron spectrum. The fissionable isotopes 233, 235, 238U, 237Np, and 239Pu were separately placed inside of this shield and irradiated under pulsed conditions at the Washington State University 1 MW TRIGA reactor. A unique set of fission product gamma spectra were collected at short times (4 minutes to 1 week) post-fission. Gamma spectra were collected on single-crystal high purity germanium detectors and on Pacific Northwest National Laboratory's (PNNL's) Direct Simultaneous Measurement (DSM) system composed of HPGe detectors connected in coincidence. This work defines the experimental methods used to produce and collect the gamma data, and demonstrates the validity of the measurements. It is important to fully document this information so the data can be used with high confidence for the advancement of nuclear science and non-proliferation applications. The gamma spectra collected in these and other experiments will be made publicly available at https://spcollab.pnl.gov/sites/gammadata or via the link at http://rdnsgroup.pnl.gov. A revised version of this publication will be posted with the data to make the experimental details available to those using the data.

  1. High-Resolution Correlated Fission Product Measurements of 235U (nth , f) with SPIDER

    NASA Astrophysics Data System (ADS)

    Shields, Dan; Spider Team

    2015-10-01

    The SPIDER detector (SPectrometer for Ion DEtermination in fission Research) has obtained high-resolution, moderate-efficiency, correlated fission product data needed for many applications including the modeling of next generation nuclear reactors, stockpile stewardship, and the fundamental understanding of the fission process. SPIDER simultaneously measures velocity and energy of both fission products to calculate fission product yields (FPYs), neutron multiplicity (ν), and total kinetic energy (TKE). These data will be some of the first of their kind available to nuclear data evaluations. An overview of the SPIDER detector, analytical method, and preliminary results for 235U (nth , f) will be presented. LA-UR-15-20130 This work benefited from the use of the LANSCE accelerator facility and was performed under the auspices of the US Department of Energy by Los Alamos Security, LLC under Contract DE-AC52-06NA25396.

  2. Partitioning of selected fission products from irradiated oxide fuel induced by thermal treatment

    NASA Astrophysics Data System (ADS)

    Shcherbina, Natalia; Kivel, Niko; Günther-Leopold, Ines

    2013-06-01

    The release of fission products (FPs) from spent nuclear fuel (SNF) has been studied as a function of the temperature and redox conditions. The present paper concerns essentially the high temperature separation of Cs and Sr from irradiated pressurized (PWR) and boiling water reactor (BWR) fuel of different burn-up levels with use of an in-house designed system for inductive vaporization (InVap). Using thermodynamic calculations with the Module of Fission Product Release (MFPR) code along with annealing experiments on SNF in the InVap it was shown that the speciation of Cs and Sr, hence their release behavior at high temperature, is sensitive to the redox conditions during thermal treatment. It was demonstrated that annealing conditions in the InVap can be adjusted in the way to promote the release of selected FPs without significant loss of the fuel matrix or actinides: complete release of Cs and I was achieved during treatment of irradiated fuel at 1800 °C under reducing atmosphere (0.7% H2/Ar mixture). The developed partitioning procedure can be used for the SNF pretreatment as an advanced head-end step in the hydrometallurgical or pyrochemical reprocessing technology.

  3. Identifying and quantifying short-lived fission products from thermal fission of HEU using portable HPGe detectors

    SciTech Connect

    Pierson, Bruce D.; Finn, Erin C.; Friese, Judah I.; Greenwood, Lawrence R.; Kephart, Jeremy D.; Kephart, Rosara F.; Metz, Lori A.

    2013-03-01

    Due to the emerging potential for trafficking of special nuclear material, research programs are investigating current capabilities of commercially available portable gamma ray detection systems. Presented in this paper are the results of three different portable high-purity germanium (HPGe) detectors used to identify short-lived fission products generated from thermal neutron interrogation of small samples of highly enriched uranium. Samples were irradiated at the Washington State University (WSU) Nuclear Radiation Center’s 1MW TRIGA reactor. The three portable, HPGe detectors used were the ORTEC MicroDetective, the ORTEC Detective, and the Canberra Falcon. Canberra’s GENIE-2000 software was used to analyze the spectral data collected from each detector. Ultimately, these three portable detectors were able to identify a large range of fission products showing potential for material discrimination.

  4. Europa's Atmosphere: Production & Loss

    NASA Astrophysics Data System (ADS)

    Bagenal, Fran; Cassidy, T.; Dols, V.; Crary, F.

    2013-10-01

    Europa is embedded not only in the ionized material of the Io plasma torus, but is also surrounded by the material (both ionized and neutral) produced by the interaction of this plasma with the moon’s surface and atmosphere - as illustrated in the schematic below. Moreover, there are energetic ions and electrons that diffuse inwards from the outer magnetosphere and interact with the moon and surrounding neutral clouds. The multiple components of Europa’s environment are thought to vary on timescales of hours to weeks and to be strongly coupled. Europa’s O2 atmosphere is created by ion bombardment of the surface. Earlier studies assumed that the energetic (10s keV) ions were responsible (see review in Smyth and Marconi, 2006). New research (Cassidy et al. 2013) suggests that the “thermal” ion population of the Io plasma torus produces most of Europa’s O2. But this cooler population is easily diverted by currents induced in Europa’s ionosphere and prevented from reaching the surface. This feedback has not been adequately explored. Modelers have historically focused on a single piece of the puzzle; plasma modelers assume a static atmosphere and atmosphere modelers assume static plasma. We are now in a position to consider these new sources of atmosphere and determine how the observed system comes about as well as quantify the timescales and causes of its evolution. This begs the question is Europa’s atmosphere-magnetosphere interaction self-regulating? We are specifically interested in how the system responds to changes - for example, how does Europa’s atmosphere change when the inflowing plasma flux increases or decreases? What is the corresponding change in the electrodynamics and diversion of plasma flow around Europa? How much and on what time scale does the extended neutral cloud respond? And what are the consequences for the influx of energetic particles? We model this coupled system to address how each component responds to changes in the

  5. Fission product behavior during the PBF (Power Burst Facility) Severe Fuel Damage Test 1-1

    SciTech Connect

    Hartwell, J K; Petti, D A; Hagrman, D L; Jensen, S M; Cronenberg, A W

    1987-05-01

    In response to the accident at Three Mile Island Unit 2 (TMI-2), the United States Nuclear Regulatory Commission (USNRC) initiated a series of Severe Fuel Damage tests that were performed in the Power Burst Facility at the Idaho National Engineering Laboratory to obtain data necessary to understand (a) fission product release, transport, and deposition; (b) hydrogen generation; and (c) fuel/cladding material behavior during degraded core accidents. Data are presented about fission product behavior noted during the second experiment of this series, the Severe Fuel Damage Test 1-1, with an in-depth analysis of the fission product release, transport, and deposition phenomena that were observed. Real-time release and transport data of certain fission products were obtained from on-line gamma spectroscopy measurements. Liquid and gas effluent grab samples were collected at selected periods during the test transient. Additional information was obtained from steamline deposition analysis. From these and other data, fission product release rates and total release fractions are estimated and compared with predicted release behavior using current models. Fission product distributions and a mass balance are also summarized, and certain probable chemical forms are predicted for iodine, cesium, and tellurium. An in-depth evaluation of phenomena affecting the behavior of the high-volatility fission products - xenon, krypton, iodine, cesium, and tellurium - is presented. Analysis indicates that volatile release from fuel is strongly influenced by parameters other than fuel temperature. Fission product behavior during transport through the Power Burst Facility effluent line to the fission product monitoring system is assessed. Tellurium release behavior is also examined relatve to the extent of Zircaloy cladding oxidation. 81 fig., 53 tabs.

  6. SEPARATION OF PLUTONIUM FROM FISSION PRODUCTS BY A COLLOID REMOVAL PROCESS

    DOEpatents

    Schubert, J.

    1960-05-24

    A method is given for separating plutonium from uranium fission products. An acidic aqueous solution containing plutonium and uranium fission products is subjected to a process for separating ionic values from colloidal matter suspended therein while the pH of the solution is maintained between 0 and 4. Certain of the fission products, and in particular, zirconium, niobium, lanthanum, and barium are in a colloidal state within this pH range, while plutonium remains in an ionic form, Dialysis, ultracontrifugation, and ultrafiltration are suitable methods of separating plutonium ions from the colloids.

  7. Deep Atomic Binding (DAB) Approach in Interpretation of Fission Products Behavior in Terrestrial and Water Ecosystems

    SciTech Connect

    Ajlouni, Abdul-Wali M.S.

    2006-07-01

    A large number of studies and models were established to explain the fission products (FP) behavior within terrestrial and water ecosystems, but a number of behaviors were non understandable, which always attributed to unknown reasons. According to DAB hypothesis, almost all fission products behaviors in terrestrial and water ecosystems could be interpreted in a wide coincidence. The gab between former models predictions, and field behavior of fission products after accidents like Chernobyl have been explained. DAB represents a tool to reduce radio-phobia as well as radiation protection expenses. (author)

  8. Background and Derivation of ANS-5.4 Standard Fission Product Release Model

    SciTech Connect

    Beyer, Carl E.; Turnbull, Andrew J.

    2010-01-29

    This background report describes the technical basis for the newly proposed American Nuclear Society (ANS) 5.4 standard, Methods for Calculating the Fractional Release of Volatile Fission Products from Oxide Fuels. The proposed ANS 5.4 standard provides a methodology for determining the radioactive fission product releases from the fuel for use in assessing radiological consequences of postulated accidents that do not involve abrupt power transients. When coupled with isotopic yields, this method establishes the 'gap activity,' which is the inventory of volatile fission products that are released from the fuel rod if the cladding are breached.

  9. Radiation Damage and Fission Product Release in Zirconium Nitride

    SciTech Connect

    Egeland, Gerald W.

    2005-08-29

    Zirconium nitride is a material of interest to the AFCI program due to some of its particular properties, such as its high melting point, strength and thermal conductivity. It is to be used as an inert matrix or diluent with a nuclear fuel based on transuranics. As such, it must sustain not only high temperatures, but also continuous irradiation from fission and decay products. This study addresses the issues of irradiation damage and fission product retention in zirconium nitride through an assessment of defects that are produced, how they react, and how predictions can be made as to the overall lifespan of the complete nuclear fuel package. Ion irradiation experiments are a standard method for producing radiation damage to a surface for observation. Cryogenic irradiations are performed to produce the maximum accumulation of defects, while elevated temperature irradiations may be used to allow defects to migrate and react to form clusters and loops. Cross-sectional transmission electron microscopy and grazing-incidence x-ray diffractometry were used in evaluating the effects that irradiation has on the crystal structure and microstructure of the material. Other techniques were employed to evaluate physical effects, such as nanoindentation and helium release measurements. Results of the irradiations showed that, at cryogenic temperatures, ZrN withstood over 200 displacements per atom without amorphization. No significant change to the lattice or microstructure was observed. At elevated temperatures, the large amount of damage showed mobility, but did not anneal significantly. Defect clustering was possibly observed, yet the size was too small to evaluate, and bubble formation was not observed. Defects, specifically nitrogen vacancies, affect the mechanical behavior of ZrN dramatically. Current and previous work on dislocations shows a distinct change in slip plane, which is evidence of the bonding characteristics. The stacking-fault energy changes dramatically with

  10. Investigation of inconsistent ENDF/B-VII.1 independent and cumulative fission product yields with proposed revisions

    SciTech Connect

    Pigni, Marco T; Francis, Matthew W; Gauld, Ian C

    2015-01-01

    A recent implementation of ENDF/B-VII. independent fission product yields and nuclear decay data identified inconsistencies in the data caused by the use of updated nuclear scheme in the decay sub-library that is not reflected in legacy fission product yield data. Recent changes in the decay data sub-library, particularly the delayed neutron branching fractions, result in calculated fission product concentrations that are incompatible with the cumulative fission yields in the library, and also with experimental measurements. A comprehensive set of independent fission product yields was generated for thermal and fission spectrum neutron induced fission for 235,238U and 239,241Pu in order to provide a preliminary assessment of the updated fission product yield data consistency. These updated independent fission product yields were utilized in the ORIGEN code to evaluate the calculated fission product inventories with experimentally measured inventories, with particular attention given to the noble gases. An important outcome of this work is the development of fission product yield covariance data necessary for fission product uncertainty quantification. The evaluation methodology combines a sequential Bayesian method to guarantee consistency between independent and cumulative yields along with the physical constraints on the independent yields. This work was motivated to improve the performance of the ENDF/B-VII.1 library in the case of stable and long-lived cumulative yields due to the inconsistency of ENDF/B-VII.1 fission p;roduct yield and decay data sub-libraries. The revised fission product yields and the new covariance data are proposed as a revision to the fission yield data currently in ENDF/B-VII.1.

  11. Investigation of Inconsistent ENDF/B-VII.1 Independent and Cumulative Fission Product Yields with Proposed Revisions

    SciTech Connect

    Pigni, M.T. Francis, M.W.; Gauld, I.C.

    2015-01-15

    A recent implementation of ENDF/B-VII.1 independent fission product yields and nuclear decay data identified inconsistencies in the data caused by the use of updated nuclear schemes in the decay sub-library that are not reflected in legacy fission product yield data. Recent changes in the decay data sub-library, particularly the delayed neutron branching fractions, result in calculated fission product concentrations that do not agree with the cumulative fission yields in the library as well as with experimental measurements. To address these issues, a comprehensive set of independent fission product yields was generated for thermal and fission spectrum neutron-induced fission for {sup 235,238}U and {sup 239,241}Pu in order to provide a preliminary assessment of the updated fission product yield data consistency. These updated independent fission product yields were utilized in the ORIGEN code to compare the calculated fission product inventories with experimentally measured inventories, with particular attention given to the noble gases. Another important outcome of this work is the development of fission product yield covariance data necessary for fission product uncertainty quantification. The evaluation methodology combines a sequential Bayesian method to guarantee consistency between independent and cumulative yields along with the physical constraints on the independent yields. This work was motivated to improve the performance of the ENDF/B-VII.1 library for stable and long-lived fission products. The revised fission product yields and the new covariance data are proposed as a revision to the fission yield data currently in ENDF/B-VII.1.

  12. Investigation of Inconsistent ENDF/B-VII.1 Independent and Cumulative Fission Product Yields with Proposed Revisions

    NASA Astrophysics Data System (ADS)

    Pigni, M. T.; Francis, M. W.; Gauld, I. C.

    2015-01-01

    A recent implementation of ENDF/B-VII.1 independent fission product yields and nuclear decay data identified inconsistencies in the data caused by the use of updated nuclear schemes in the decay sub-library that are not reflected in legacy fission product yield data. Recent changes in the decay data sub-library, particularly the delayed neutron branching fractions, result in calculated fission product concentrations that do not agree with the cumulative fission yields in the library as well as with experimental measurements. To address these issues, a comprehensive set of independent fission product yields was generated for thermal and fission spectrum neutron-induced fission for 235,238U and 239,241Pu in order to provide a preliminary assessment of the updated fission product yield data consistency. These updated independent fission product yields were utilized in the ORIGEN code to compare the calculated fission product inventories with experimentally measured inventories, with particular attention given to the noble gases. Another important outcome of this work is the development of fission product yield covariance data necessary for fission product uncertainty quantification. The evaluation methodology combines a sequential Bayesian method to guarantee consistency between independent and cumulative yields along with the physical constraints on the independent yields. This work was motivated to improve the performance of the ENDF/B-VII.1 library for stable and long-lived fission products. The revised fission product yields and the new covariance data are proposed as a revision to the fission yield data currently in ENDF/B-VII.1.

  13. Prompt γ-ray production in neutron-induced fission of 239Pu

    NASA Astrophysics Data System (ADS)

    Ullmann, J. L.; Bond, E. M.; Bredeweg, T. A.; Couture, A.; Haight, R. C.; Jandel, M.; Kawano, T.; Lee, H. Y.; O'Donnell, J. M.; Hayes, A. C.; Stetcu, I.; Taddeucci, T. N.; Talou, P.; Vieira, D. J.; Wilhelmy, J. B.; Becker, J. A.; Chyzh, A.; Gostic, J.; Henderson, R.; Kwan, E.; Wu, C. Y.

    2013-04-01

    Background: The prompt gamma-ray spectrum from fission is important for understanding the physics of nuclear fission, and also in applications involving fission. Relatively few measurements of the prompt gamma spectrum from 239Pu(n,f) have been published.Purpose: This experiment measured the multiplicity, individual gamma energy spectrum, and total gamma energy spectrum of prompt fission gamma rays from 239Pu(n,f) in the neutron energy range from thermal to 30 keV, to test models of fission and to provide information for applications.Method: Gamma rays from neutron-induced fission of 239Pu were measured using the DANCE gamma-ray calorimeter. Fission events were tagged by detecting fission products in a parallel-plate avalanche counter in the center of DANCE. The measurements were corrected for detector response using a geant4 model of DANCE. A detailed analysis for the gamma rays from the 1+ resonance complex at 10.93 eV is presented.Results: A six-parameter analytical parametrization of the fission gamma-ray spectrum was obtained. A Monte Carlo Hauser-Feshbach calculation provided good general agreement with the data, but some differences remain to be resolved.Conclusions: An analytic parametrization can be made of the gamma-ray multiplicity, energy distribution, and total-energy distribution for the prompt gamma rays following neutron-induced fission of 239Pu. This parametrization may be useful for applications. Modern Monte Carlo Hauser-Feshbach calculations can do a good job of calculating the fission gamma-ray emission spectrum, although some details remain to be understood.

  14. Baseline Glass Development for Combined Fission Products Waste Streams

    SciTech Connect

    Crum, Jarrod V.; Billings, Amanda Y.; Lang, Jesse B.; Marra, James C.; Rodriguez, Carmen P.; Ryan, Joseph V.; Vienna, John D.

    2009-06-29

    Borosilicate glass was selected as the baseline technology for immobilization of the Cs/Sr/Ba/Rb (Cs), lanthanide (Ln) and transition metal fission product (TM) waste steams as part of a cost benefit analysis study.[1] Vitrification of the combined waste streams have several advantages, minimization of the number of waste forms, a proven technology, and similarity to waste forms currently accepted for repository disposal. A joint study was undertaken by Pacific Northwest National Laboratory (PNNL) and Savannah River National Laboratory (SRNL) to develop acceptable glasses for the combined Cs + Ln + TM waste streams (Option 1) and Cs + Ln combined waste streams (Option 2) generated by the AFCI UREX+ set of processes. This study is aimed to develop baseline glasses for both combined waste stream options and identify key waste components and their impact on waste loading. The elemental compositions of the four-corners study were used along with the available separations data to determine the effect of burnup, decay, and separations variability on estimated waste stream compositions.[2-5] Two different components/scenarios were identified that could limit waste loading of the combined Cs + LN + TM waste streams, where as the combined Cs + LN waste stream has no single component that is perceived to limit waste loading. Combined Cs + LN waste stream in a glass waste form will most likely be limited by heat due to the high activity of Cs and Sr isotopes.

  15. Fission products from the damaged Fukushima reactor observed in Hungary.

    PubMed

    Bihari, Árpád; Dezső, Zoltán; Bujtás, Tibor; Manga, László; Lencsés, András; Dombóvári, Péter; Csige, István; Ranga, Tibor; Mogyorósi, Magdolna; Veres, Mihály

    2014-01-01

    Fission products, especially (131)I, (134)Cs and (137)Cs, from the damaged Fukushima Dai-ichi nuclear power plant (NPP) were detected in many places worldwide shortly after the accident caused by natural disaster. To observe the spatial and temporal variation of these isotopes in Hungary, aerosol samples were collected at five locations from late March to early May 2011: Institute of Nuclear Research, Hungarian Academy of Sciences (ATOMKI, Debrecen, East Hungary), Paks NPP (Paks, South-Central Hungary) as well as at the vicinity of Aggtelek (Northeast Hungary), Tapolca (West Hungary) and Bátaapáti (Southwest Hungary) settlements. In addition to the aerosol samples, dry/wet fallout samples were collected at ATOMKI, and airborne elemental iodine and organic iodide samples were collected at Paks NPP. The peak in the activity concentration of airborne (131)I was observed around 30 March (1-3 mBq m(-3) both in aerosol samples and gaseous iodine traps) with a slow decline afterwards. Aerosol samples of several hundred cubic metres of air showed (134)Cs and (137)Cs in detectable amounts along with (131)I. The decay-corrected inventory of (131)I fallout at ATOMKI was 2.1±0.1 Bq m(-2) at maximum in the observation period. Dose-rate contribution calculations show that the radiological impact of this event at Hungarian locations was of no considerable concern.

  16. Determination of {sup 140}La fission product interference factor for INAA

    SciTech Connect

    Ribeiro Jr, Iberê S.; Genezini, Frederico A.; Saiki, Mitiko; Zahn, Guilherme S.

    2014-11-11

    Instrumental Neutron Activation Analysis (INAA) is a technique widely used to determine the concentration of several elements in several kinds of matrices. However if the sample of interest has higher relative uranium concentration the obtained results can be interfered by the uranium fission products. One of these cases that is affected by interference due to U fission is the {sup 140}La, because this radioisotope used in INAA for the determination of concentration the La is also produced by the {sup −}β of {sup 140}Ba, an uranium fission product. The {sup 140}La interference factor was studied in this work and a factor to describe its time dependence was obtained.

  17. ARSENATE CARRIER PRECIPITATION METHOD OF SEPARATING PLUTONIUM FROM NEUTRON IRRADIATED URANIUM AND RADIOACTIVE FISSION PRODUCTS

    DOEpatents

    Thompson, S.G.; Miller, D.R.; James, R.A.

    1961-06-20

    A process is described for precipitating Pu from an aqueous solution as the arsenate, either per se or on a bismuth arsenate carrier, whereby a separation from uranium and fission products, if present in solution, is accomplished.

  18. The LANL C-NR counting room and fission product yields

    SciTech Connect

    Jackman, Kevin Richard

    2015-09-21

    This PowerPoint presentation focused on the following areas: LANL C-NR counting room; Fission product yields; Los Alamos Neutron wheel experiments; Recent experiments ad NCERC; and Post-detonation nuclear forensics

  19. Photon-induced Fission Product Yield Measurements on 235U, 238U, and 239Pu

    NASA Astrophysics Data System (ADS)

    Krishichayan, Fnu; Bhike, M.; Tonchev, A. P.; Tornow, W.

    2015-10-01

    During the past three years, a TUNL-LANL-LLNL collaboration has provided data on the fission product yields (FPYs) from quasi-monoenergetic neutron-induced fission of 235U, 238U, and 239Pu at TUNL in the 0.5 to 15 MeV energy range. Recently, we have extended these experiments to photo-fission. We measured the yields of fission fragments ranging from 85Kr to 147Nd from the photo-fission of 235U, 238U, and 239Pu using 13-MeV mono-energetic photon beams at the HIGS facility at TUNL. First of its kind, this measurement will provide a unique platform to explore the effect of the incoming probe on the FPYs, i.e., photons vs. neutrons. A dual-fission ionization chamber was used to determine the number of fissions in the targets and these samples (along with Au monitor foils) were gamma-ray counted in the low-background counting facility at TUNL. Details of the experimental set-up and results will be presented and compared to the FPYs obtained from neutron-induced fission at the same excitation energy of the compound nucleus. Work supported in part by the NNSA-SSAA Grant No. DE-NA0001838.

  20. RARE-EARTH METAL FISSION PRODUCTS FROM LIQUID U-Bi

    DOEpatents

    Wiswall, R.H.

    1960-05-10

    Fission product metals can be removed from solution in liquid bismuth without removal of an appreciable quantity of uranium by contacting the liquid metal solution with fused halides, as for example, the halides of sodium, potassium, and lithium and by adding to the contacted phases a quantity of a halide which is unstable relative to the halides of the fission products, a specific unstable halide being MgCl/sub 3/.

  1. Using gamma spectrometry indicators to detect and quantify fission products changes in irradiated fuel

    SciTech Connect

    Loubet, L.; Martella, Th.

    2015-07-01

    A new analysis method based on gamma scanning of fission products on irradiated rods is presented. Indicators calculated from this method can be used for the qualitative treatment and comparison of irradiated rods from PWR, SFR or and MTR. Differences in the behavior of fission products (FP) can thus be quantified. Phenomena such as migration or geometrical changes in pellets should thus benefit from these accurate, yet quickly and easily achievable results. (authors)

  2. Nuclear data evaluation of long-lived fission products: Microscopic vs. phenomenological optical potentials

    NASA Astrophysics Data System (ADS)

    Minato, Futoshi; Iwamoto, Osamu; Minomo, Kosho; Ogata, Kazuyuki; Iwamoto, Nobuyuki; Kunieda, Satoshi; Furutachi, Naoya

    2017-09-01

    Neutron-nucleus cross sections calculated by macroscopic potentials are compared with a microscopic one to study the performance for long-lived fission products. The macroscopic potentials show a good agreement with the microscopic one at higher energies, where neutron experimental data are scarce. Besides it, analyses of differential elastic cross sections at low energies also suggest that the macroscopic potentials are still effective and applicable enough for the long-lived fission products.

  3. New Fission-Product Waste Forms: Development and Characterization

    SciTech Connect

    Alexandra Navrotsky

    2010-07-30

    Research performed on the program “New Fission Product Waste Forms: Development and Characterization,” in the last three years has fulfilled the objectives of the proposal which were to 1) establish ceramic waste forms for disposing of Cs, Sr and minor actinides, 2) fully characterize the phase relationships, structures and thermodynamic and kinetic stabilities of promising waste forms, 3) establish a sound technical basis for understanding key waste form properties, such as melting temperatures and aqueous durability, based on an in-depth understanding of waste form structures and thermochemistry, and 4) establish synthesis, testing, scaleup and commercialization routes for wasteform implementation through out in-kind collaborations. In addition, since Cs and Sr form new elements by radioactive decay, the behavior and thermodynamics of waste forms containing different proportions of Cs, Sr and their decay products were discovered using non-radioactive analogues. Collaborations among researchers from three institutions, UC Davis, Sandia National Laboratories, and Shott Inc., were formed to perform the primary work on the program. The unique expertise of each of the members in the areas of waste form development, structure/property relationships, hydrothermal and high temperature synthesis, crystal/glass production, and thermochemistry was critical to program success. In addition, collaborations with the Brigham Young Univeristy, Ben Gurion University, and Los Alamos National Laboratory, were established for standard entropies of ceramic waste forms, sol-gel synthesis, and high temperature synthesis. This work has had a significant impact in a number of areas. First, the studies of the thermodynamic stability of the mineral analogues provided an important technical foundation for assessment the viability of multicomponent oxide phases for Cs and Sr removal. Moreover, the thermodynamic data discovered in this program established information on the reaction

  4. Diffusion of Zr, Ru, Ce, Y, La, Sr and Ba fission products in UO2

    NASA Astrophysics Data System (ADS)

    Perriot, R.; Liu, X.-Y.; Stanek, C. R.; Andersson, D. A.

    2015-04-01

    The diffusivity of the solid fission products (FP) Zr (Zr4+), Ru (Ru4+, Ru3+), Ce (Ce4+), Y (Y3+), La (La3+), Sr (Sr2+) and Ba (Ba2+) by a vacancy mechanism has been calculated, using a combination of density functional theory (DFT) and empirical potential (EP) calculations. The activation energies for the solid fission products are compared to the activation energy for Xe fission gas atoms calculated previously. Apart from Ru, the solid fission products all exhibit higher activation energy than Xe. For all solid FPs except Y3+, the migration of the FP has lower barrier than the migration of a neighboring U atom, making the latter the rate limiting step for direct migration. An indirect mechanism, consisting of two successive migrations around the FP, is also investigated. The calculated diffusivities show that most solid fission products diffuse with rates similar to U self-diffusion. However, Ru, Ba and Sr exhibit faster diffusion than the other solid FPs, with Ru3+ and Ru4+ diffusing even faster than Xe for T < 1200 K. The diffusivities correlate with the observed fission product solubility in UO2, and the tendency to form metallic and oxide second phase inclusions.

  5. Detecting special nuclear materials in containers using high-energy gamma rays emitted by fission products

    DOEpatents

    Norman, Eric B.; Prussin, Stanley G.

    2007-10-02

    A method and a system for detecting the presence of special nuclear materials in a container. The system and its method include irradiating the container with an energetic beam, so as to induce a fission in the special nuclear materials, detecting the gamma rays that are emitted from the fission products formed by the fission, to produce a detector signal, comparing the detector signal with a threshold value to form a comparison, and detecting the presence of the special nuclear materials using the comparison.

  6. Simulating γ-γ coincidences of β-delayed γ-rays from fission product nuclei

    NASA Astrophysics Data System (ADS)

    Padgett, Stephen; Wang, Tzu-Fang

    2015-01-01

    Analyzing radiation from material that has undergone neutron induced fission is important for fields such as nuclear forensics, reactor physics, and nonproliferation monitoring. The γ-ray spectroscopy of fission products is a major part of the characterization of a material's fissile inventory and the energy of incident neutrons inducing fission. Cumulative yields and γ-ray intensities from nuclear databases are inputs into a GEANT4 simulation to create expected γ-ray spectra from irradiated 235U. The simulations include not only isotropically emitted γ-rays but also γ-γ cascades from certain fission products, emitted with their appropriate angular correlations. Here γ singles spectra as well as γ-γ coincidence spectra are simulated in detectors at both 90° and 180° pairings. The ability of these GEANT4 Monte Carlo simulations to duplicate experimental data is explored in this work. These simulations demonstrate potential in exploiting angular correlations of γ-γ cascades in fission product decays to determine isotopic content. Analyzing experimental and simulated γ-γ coincidence spectra as opposed to singles spectra should improve the ability to identify fission product nuclei since such spectra are cleaner and contain more resolved peaks when compared to γ singles spectra.

  7. Photo-fission for the production of radioactive beams ALTO project

    NASA Astrophysics Data System (ADS)

    Essabaa, S.; Arianer, J.; Ausset, P.; Bajeat, O.; Baronick, J. P.; Clapier, F.; Coacolo, L.; Donzaud, C.; Ducourtieux, M.; Galès, S.; Gardès, D.; Grialou, D.; Hosni, F.; Guillemaud-Mueller, D.; Ibrahim, F.; Junquera, T.; Lau, C.; Le Blanc, F.; Lefort, H.; Le Scornet, J. C.; Lesrel, J.; Mueller, A. C.; Obert, J.; Perru, O.; Potier, J. C.; Proust, J.; Pougheon, F.; Roussière, B.; Rouvière, N.; Sauvage, J.; Sorlin, O.; Tkatchenko, A.; Verney, D.; Waast, B.; Rinolfi, L.; Rossat, G.; Forkel-Wirth, D.; Muller, A.; Bienvenu, G.; Bourdon, J.-C.; Garvey, T.; Jacquemard, B.; Omeich, M.

    2003-05-01

    In order to probe neutron rich radioactive noble gases produced by photo-fission, a PARRNe-1 experiment (Production d'Atomes Radioactifs Riches en Neutrons) has been carried out at CERN. The incident electron beam of 50 MeV was delivered by the LIL machine: LEP Injector Linac. The experiment allowed us to compare under the same conditions two production methods of radioactive noble gases: fission induced by fast neutrons and photo-fission. The obtained results show that the use of the electrons is a promising mode to get intense neutron rich ion beams. After the success of this photo-fission experiment, a conceptual design for the installation at IPN Orsay of a 50 MeV electron accelerator close to the PARRNe-2 device has been worked out: ALTO Project. This work has started within a collaboration between IPNO, LAL (Laboratoire de l'Accélérateur Linéaire) and CERN groups.

  8. Relative fission product yield determination in the USGS TRIGA Mark I reactor

    NASA Astrophysics Data System (ADS)

    Koehl, Michael A.

    Fission product yield data sets are one of the most important and fundamental compilations of basic information in the nuclear industry. This data has a wide range of applications which include nuclear fuel burnup and nonproliferation safeguards. Relative fission yields constitute a major fraction of the reported yield data and reduce the number of required absolute measurements. Radiochemical separations of fission products reduce interferences, facilitate the measurement of low level radionuclides, and are instrumental in the analysis of low-yielding symmetrical fission products. It is especially useful in the measurement of the valley nuclides and those on the extreme wings of the mass yield curve, including lanthanides, where absolute yields have high errors. This overall project was conducted in three stages: characterization of the neutron flux in irradiation positions within the U.S. Geological Survey TRIGA Mark I Reactor (GSTR), determining the mass attenuation coefficients of precipitates used in radiochemical separations, and measuring the relative fission products in the GSTR. Using the Westcott convention, the Westcott flux, modified spectral index, neutron temperature, and gold-based cadmium ratios were determined for various sampling positions in the USGS TRIGA Mark I reactor. The differential neutron energy spectrum measurement was obtained using the computer iterative code SAND-II-SNL. The mass attenuation coefficients for molecular precipitates were determined through experiment and compared to results using the EGS5 Monte Carlo computer code. Difficulties associated with sufficient production of fission product isotopes in research reactors limits the ability to complete a direct, experimental assessment of mass attenuation coefficients for these isotopes. Experimental attenuation coefficients of radioisotopes produced through neutron activation agree well with the EGS5 calculated results. This suggests mass attenuation coefficients of molecular

  9. Evaluation of fission product worth margins in PWR spent nuclear fuel burnup credit calculations.

    SciTech Connect

    Blomquist, R.N.; Finck, P.J.; Jammes, C.; Stenberg, C.G.

    1999-02-17

    Current criticality safety calculations for the transportation of irradiated LWR fuel make the very conservative assumption that the fuel is fresh. This results in a very substantial overprediction of the actual k{sub eff} of the transportation casks; in certain cases, this decreases the amount of spent fuel which can be loaded in a cask, and increases the cost of transporting the spent fuel to the repository. Accounting for the change of reactivity due to fuel depletion is usually referred to as ''burnup credit.'' The US DOE is currently funding a program aimed at establishing an actinide only burnup credit methodology (in this case, the calculated reactivity takes into account the buildup or depletion of a limited number of actinides). This work is undergoing NRC review. While this methodology is being validated on a significant experimental basis, it implicitly relies on additional margins: in particular, the absorption of neutrons by certain actinides and by all fission products is not taken into account. This provides an important additional margin and helps guarantee that the methodology is conservative provided these neglected absorption are known with reasonable accuracy. This report establishes the accuracy of fission product absorption rate calculations: (1) the analysis of European fission product worth experiments demonstrates that fission product cross-sections available in the US provide very good predictions of fission product worth; (2) this is confirmed by a direct comparison of European and US cross section evaluations; (3) accuracy of Spent Nuclear Fuel (SNF) fission product content predictions is established in a recent ORNL report where several SNF isotopic assays are analyzed; and (4) these data are then combined to establish in a conservative manner the fraction of the predicted total fission product absorption which can be guaranteed based on available experimental data.

  10. Fusion-Fission Hybrid for Fissile Fuel Production without Processing

    SciTech Connect

    Fratoni, M; Moir, R W; Kramer, K J; Latkowski, J F; Meier, W R; Powers, J J

    2012-01-02

    Two scenarios are typically envisioned for thorium fuel cycles: 'open' cycles based on irradiation of {sup 232}Th and fission of {sup 233}U in situ without reprocessing or 'closed' cycles based on irradiation of {sup 232}Th followed by reprocessing, and recycling of {sup 233}U either in situ or in critical fission reactors. This study evaluates a third option based on the possibility of breeding fissile material in a fusion-fission hybrid reactor and burning the same fuel in a critical reactor without any reprocessing or reconditioning. This fuel cycle requires the hybrid and the critical reactor to use the same fuel form. TRISO particles embedded in carbon pebbles were selected as the preferred form of fuel and an inertial laser fusion system featuring a subcritical blanket was combined with critical pebble bed reactors, either gas-cooled or liquid-salt-cooled. The hybrid reactor was modeled based on the earlier, hybrid version of the LLNL Laser Inertial Fusion Energy (LIFE1) system, whereas the critical reactors were modeled according to the Pebble Bed Modular Reactor (PBMR) and the Pebble Bed Advanced High Temperature Reactor (PB-AHTR) design. An extensive neutronic analysis was carried out for both the hybrid and the fission reactors in order to track the fuel composition at each stage of the fuel cycle and ultimately determine the plant support ratio, which has been defined as the ratio between the thermal power generated in fission reactors and the fusion power required to breed the fissile fuel burnt in these fission reactors. It was found that the maximum attainable plant support ratio for a thorium fuel cycle that employs neither enrichment nor reprocessing is about 2. This requires tuning the neutron energy towards high energy for breeding and towards thermal energy for burning. A high fuel loading in the pebbles allows a faster spectrum in the hybrid blanket; mixing dummy carbon pebbles with fuel pebbles enables a softer spectrum in the critical reactors

  11. Addressing Fission Product Validation in MCNP Burnup Credit Criticality Calculations

    SciTech Connect

    Mueller, Don; Bowen, Douglas G; Marshall, William BJ J

    2015-01-01

    The US Nuclear Regulatory Commission (NRC) Division of Spent Fuel Storage and Transportation issued Interim Staff Guidance (ISG) 8, Revision 3 in September 2012. This ISG provides guidance for NRC staff members’ review of burnup credit (BUC) analyses supporting transport and dry storage of pressurized water reactor spent nuclear fuel (SNF) in casks. The ISG includes guidance for addressing validation of criticality (keff) calculations crediting the presence of a limited set of fission products and minor actinides (FP&MAs). Based on previous work documented in NRC Regulatory Guide (NUREG) Contractor Report (CR)-7109, the ISG recommends that NRC staff members accept the use of either 1.5 or 3% of the FP&MA worth—in addition to bias and bias uncertainty resulting from validation of keff calculations for the major actinides in SNF—to conservatively account for the bias and bias uncertainty associated with the specified unvalidated FP&MAs. The ISG recommends (1) use of 1.5% of the FP&MA worth if a modern version of SCALE and its nuclear data are used and (2) 3% of the FP&MA worth for well qualified, industry standard code systems other than SCALE with the Evaluated Nuclear Data Files, Part B (ENDF/B),-V, ENDF/B-VI, or ENDF/B-VII cross sections libraries. The work presented in this paper provides a basis for extending the use of the 1.5% of the FP&MA worth bias to BUC criticality calculations performed using the Monte Carlo N-Particle (MCNP) code. The extended use of the 1.5% FP&MA worth bias is shown to be acceptable by comparison of FP&MA worths calculated using SCALE and MCNP with ENDF/B-V, -VI, and -VII–based nuclear data. The comparison supports use of the 1.5% FP&MA worth bias when the MCNP code is used for criticality calculations, provided that the cask design is similar to the hypothetical generic BUC-32 cask model and that the credited FP&MA worth is no more than 0.1 Δkeff (ISG-8, Rev. 3, Recommendation 4).

  12. Mechanistic modelling of urania fuel evolution and fission product migration during irradiation and heating

    NASA Astrophysics Data System (ADS)

    Veshchunov, M. S.; Dubourg, R.; Ozrin, V. D.; Shestak, V. E.; Tarasov, V. I.

    2007-05-01

    The models of the mechanistic code MFPR (Module for Fission Product Release) developed by IBRAE in collaboration with IRSN are described briefly in the first part of the paper. The influence of microscopic defects in the UO2 crystal structure on fission-gas transport out of grains and release from fuel pellets is described. These defects include point defects such as vacancies, interstitials and fission atoms, and extended defects such as bubbles, pores and dislocations. The mechanistic description of chemically active elements behaviour (fission-induced) is based on complex association of diffusion-vaporisation mechanism involving multi-phase and multi-component thermo-chemical equilibrium at the grain boundary with accurate calculation of fuel oxidation. In the second part, results of the code applications are given to different situations: normal LWR reactor operation, high temperature annealing, loss of coolant accident (LOCA) and severe accidents conditions.

  13. Atmospheric science and power production

    SciTech Connect

    Randerson, D.

    1984-07-01

    This is the third in a series of scientific publications sponsored by the US Atomic Energy Commission and the two later organizations, the US Energy Research and Development Adminstration, and the US Department of Energy. The first book, Meteorology and Atomic Energy, was published in 1955; the second, in 1968. The present volume is designed to update and to expand upon many of the important concepts presented previously. However, the present edition draws heavily on recent contributions made by atmospheric science to the analysis of air quality and on results originating from research conducted and completed in the 1970s. Special emphasis is placed on how atmospheric science can contribute to solving problems relating to the fate of combustion products released into the atmosphere. The framework of this book is built around the concept of air-quality modeling. Fundamentals are addressed first to equip the reader with basic background information and to focus on available meteorological instrumentation and to emphasize the importance of data management procedures. Atmospheric physics and field experiments are described in detail to provide an overview of atmospheric boundary layer processes, of how air flows around obstacles, and of the mechanism of plume rise. Atmospheric chemistry and removal processes are also detailed to provide fundamental knowledge on how gases and particulate matter can be transformed while in the atmosphere and how they can be removed from the atmosphere. The book closes with a review of how air-quality models are being applied to solve a wide variety of problems. Separate analytics have been prepared for each chapter.

  14. The rate of decay of fresh fission products from a nuclear reactor

    NASA Astrophysics Data System (ADS)

    Dolan, David J.

    Determining the rate of decay of fresh fission products from a nuclear reactor is complex because of the number of isotopes involved, different types of decay, half-lives of the isotopes, and some isotopes decay into other radioactive isotopes. Traditionally, a simplified rule of 7s and 10s is used to determine the dose rate from nuclear weapons and can be to estimate the dose rate from fresh fission products of a nuclear reactor. An experiment was designed to determine the dose rate with respect to time from fresh fission products of a nuclear reactor. The experiment exposed 0.5 grams of unenriched Uranium to a fast and thermal neutron flux from a TRIGA Research Reactor (Lakewood, CO) for ten minutes. The dose rate from the fission products was measured by four Mirion DMC 2000XB electronic personal dosimeters over a period of six days. The resulting dose rate following a rule of 10s: the dose rate of fresh fission products from a nuclear reactor decreases by a factor of 10 for every 10 units of time.

  15. Fission Product Removal From Spent Oxide Fuel By Head-End Processing

    SciTech Connect

    B. R. Westphal; K. J. Bateman; R. P. Lind; K. L. Howden; G. D. Del Cul

    2005-10-01

    The development of a head-end processing step for spent oxide fuel that applies to both aqueous and pyrometallurgical technologies is being performed by the Idaho National Laboratory, the Oak Ridge National Laboratory, and the Korean Atomic Energy Research Institute through a joint International Nuclear Energy Research Initiative. The processing step employs high temperatures and oxidative gases to promote the oxidation of UO2 to U3O8. Potential benefits of the head-end step include the removal or reduction of fission products as well as separation of the fuel from cladding. Experiments have been performed with irradiated oxide fuel to evaluate the removal of fission products. During these experiments, operating parameters such as temperature and pressure have been varied to discern their effects on the behavior of specific fission products. In general, the extent of removal increases with increasing operating temperature and decreasing pressure. Removal efficiencies as high as 98% have been achieved during testing. Given the results of testing, an explanation of the likely fission product species being removed during the test program is also provided. In addition, experiments have been performed with other oxidative gases (steam and ozone) on surrogates to determine their potential benefit for removal of fission products.

  16. Production of fission and activation product isotopes at Sandia National Laboratories

    SciTech Connect

    Coats, R.L.

    1997-08-01

    The mission of the Sandia National Laboratories (SNL) Annular Core Research Reactor (ACRR) and the Hot Cell Facility (HCF) has recently changed from support of Defense and other programs to support of the Department of Energy (DOE) Isotope Production and Distribution Program (IPDP). SNL`s primary role, in support of IPDP, is ensuring a reliable supply of {sup 99}Mo to the US health care system. SNL will also play a role of complementing the isotope production of other DOE Reactor facilities such as High Flux Isotope Reactor (HFIR) at Oak Ridge, Tennessee; High Flux Beam Reactor (HFBR) at Brookhaven, New York, ad Advanced Test Reactor (ATR) in Idaho. The unique characteristics that the SNL facilities offer to the IPDP facility capability are simplicity, multiple irradiation locations, ready irradiation space access and co-located hot cell facilities capable of processing a short decay fission product stream. The SNL {sup 99}Mo effort is characterized elsewhere and this paper is intended to describe the production of additional isotopes for that can be produced medical and other uses planned to start soon after the {sup 99}Mo capability has been established. Isotope production in the SNL facilities is through fission or by neutron activation.

  17. Continuous fission-product monitor system at Oyster Creek. Final report

    SciTech Connect

    Collins, L.L.; Chulick, E.T.

    1980-10-01

    A continuous on-line fission product monitor has been installed at the Oyster Creek Nuclear Generating Station, Forked River, New Jersey. The on-line monitor is a minicomputer-controlled high-resolution gamma-ray spectrometer system. An intrinsic Ge detector scans a collimated sample line of coolant from one of the plant's recirculation loops. The minicomputer is a Nuclear Data 6620 system. Data were accumulated for the period from April 1979 through January 1980, the end of cycle 8 for the Oyster Creek plant. Accumulated spectra, an average of three a day, were stored on magnetic disk and subsequently analyzed for fisson products, Because of difficulties in measuring absolute detector efficiency, quantitative fission product concentrations in the coolant could not be determined. Data for iodine fission products are reported as a function of time. The data indicate the existence of fuel defects in the Oyster Creek core during cycle 8.

  18. Partitioning of fission products from irradiated nitride fuel using inductive vaporization

    SciTech Connect

    Shcherbina, N.; Kulik, D.A.; Kivel, N.; Potthast, H.D.; Guenther-Leopold, I.

    2013-07-01

    Irradiated nitride fuel (Pu{sub 0.3}Zr{sub 0.7})N fabricated at PSI in frame of the CONFIRM project and having a burn-up of 10.4 % FIMA (Fission per Initial Metal Atom) has been investigated by means of inductive vaporization. The study of thermal stability and release behavior of Pu, Am, Zr and fission products (FPs) was performed in a wide temperature range (up to 2300 C. degrees) and on different redox conditions. On-line monitoring by ICP-MS detected low nitride stability and significant loss of Pu and Am at T>1900 C. degrees during annealing under inert atmosphere (Ar). The oxidative pre-treatment of nitride fuel on air at 1000 C. degrees resulted in strong retention of Pu and Am in the solid, as well as of most FPs. Thermodynamic modelling of elemental speciation using GEM-Selektor v.3 code (Gibbs Energy Minimization Selektor), supported by a comprehensive literature review on thermodynamics of actinides and FPs, revealed a number of binary compounds of Cs, Mo, Te, Sr and Ba to occur in the solid. Speciation of some FPs in the fuel is discussed and compared to earlier results of electron probe microanalysis (EPMA). Predominant vapor species predicted by GEM-Selektor calculations were Pu(g), Am(g) and N{sub 2}. Nitrogen can be completely released from the fuel after complete oxidation at 1000 C. degrees. With regard to the irradiated nitride reprocessing technology, this result can have an important practical application as an alternative way for {sup 15}N recovery. (authors)

  19. Migration of fission products at the Nevada Test Site: Detection with an isotopic tracer

    SciTech Connect

    Thompton, J.L.; Gilmore, J.S. )

    1989-01-01

    Researchers at Los Alamos National Laboratory are studying the migration of fission products away from explosion cavities formed by underground nuclear tests at the Nevada Test Site. In some cases, the isotopic composition of the fission products or activation products associated with a particular test are distinctive and we may identify them many years after the event. In this paper we describe a case in which we used rhodium isotopes to identify the source of radioactive material that had moved some 350 m from the explosion site. 4 refs., 2 figs., 2 tabs.

  20. On the Radiochemical Separations of the Beta-emitting Fission Products

    NASA Astrophysics Data System (ADS)

    Chang, Zheng; Sudowe, Ralf

    2013-04-01

    This research aims at developing fast and effective radiochemical procedures for separation of the beta-emitting fission products that are difficult to analyze by gamma-spectrometry. Post-detonation analysis, as one of the major tasks of nuclear forensics, can provide crucial information for identification of the explosion levels, fuel sources, and industrial processes of a nuclear device. However, a dozen of radionuclides with high fission yields such as Zr-93, Tc-99, Sr-90 are either pure beta-emitters or only emitting gamma-rays that are difficult to analyze. Although the analysis of these radionuclides was thoroughly studied, samples from unknown nuclear detonations can be complicated by the number of fission products, radioactivity levels, sample matrices, and time limits for analysis. The challenge facing the forensic analysis should not be underestimated. A sequential separation procedure is designed to analyze the major beta-emitting fission products. Radiochemical techniques such as solvent extraction, precipitation, and column chromatography are utilized. The procedure will be tested and improved by experiments. The final procedure should be capable of analyzing the fission products under various sample conditions effectively and rapidly.

  1. Trapping and diffusion of fission products in ThO2 and CeO2

    SciTech Connect

    Xiao, Haiyan; Zhang, Yanwen; Weber, William J

    2011-01-01

    The trapping and diffusion of Br, Rb, Cs and Xe in ThO2 and CeO{sub 2} have been studied using an Ab Initio total energy method in the local-density approximation of density functional theory. Fission products incorporated in cation mono-vacancy, cation-anion di-vacancy and Schottky defect sites are found to be stable, with the cation mono-vacancy being the preferred site in most cases. In both oxides, Rb and Cs are the most likely to be trapped, and Xe is more difficult to incorporate than other fission products. The energy barriers for migration of each species in ThO{sub 2} and CeO{sub 2} are also calculated. Alkali metals are relatively more mobile than other fission products, and bromine is the least mobile.

  2. Fission product release modelling for application of fuel-failure monitoring and detection - An overview

    NASA Astrophysics Data System (ADS)

    Lewis, B. J.; Chan, P. K.; El-Jaby, A.; Iglesias, F. C.; Fitchett, A.

    2017-06-01

    A review of fission product release theory is presented in support of fuel-failure monitoring analysis for the characterization and location of defective fuel. This work is used to describe: (i) the development of the steady-state Visual_DETECT code for coolant activity analysis to characterize failures in the core and the amount of tramp uranium; (ii) a generalization of this model in the STAR code for prediction of the time-dependent release of iodine and noble gas fission products to the coolant during reactor start-up, steady-state, shutdown, and bundle-shifting manoeuvres; (iii) an extension of the model to account for the release of fission products that are delayed-neutron precursors for assessment of fuel-failure location; and (iv) a simplification of the steady-state model to assess the methodology proposed by WANO for a fuel reliability indicator for water-cooled reactors.

  3. PROCESS USING BISMUTH PHOSPHATE AS A CARRIER PRECIPITATE FOR FISSION PRODUCTS AND PLUTONIUM VALUES

    DOEpatents

    Finzel, T.G.

    1959-03-10

    A process is described for separating plutonium from fission products carried therewith when plutonium in the reduced oxidation state is removed from a nitric acid solution of irradiated uranium by means of bismuth phosphate as a carrier precipitate. The bismuth phosphate carrier precipitate is dissolved by treatment with nitric acid and the plutonium therein is oxidized to the hexavalent oxidation state by means of potassium dichromate. Separation of the plutonium from the fission products is accomplished by again precipitating bismuth phosphate and removing the precipitate which now carries the fission products and a small percentage of the plutonium present. The amount of plutonium carried in this last step may be minimized by addition of sodium fluoride, so as to make the solution 0.03N in NaF, prior to the oxidation and prccipitation step.

  4. New human data versus estimates of effects of inhaling fission product mixtures.

    PubMed

    Brodsky, Allen; Reeves, Glen

    2009-01-01

    Recently, data on exposures of humans as well as animals to fission products in plumes emitted by underground Soviet tests have been declassified by the Khazakhstan government and published in English. Similar human intakes of gross fission product mixtures that caused acute prodromal symptoms have not been previously reported. Animal experiments with such complex mixtures have not received sufficient support to provide data that could be reliably extrapolated with dose-response models to humans for use in triage of internally exposed persons. This commentary compares some of the acute prodromal effects on humans from the recently released Soviet data with the estimates of Cowan and Kuper, and later estimates by Brodsky and colleagues. The latter estimates are concluded to be safer, and more easily adaptable, for use in triage of persons exposed to internal deposition of fission products of various mixtures.

  5. Immobilization of fission products arising from pyrometallurgical reprocessing in chloride media

    NASA Astrophysics Data System (ADS)

    Leturcq, G.; Grandjean, A.; Rigaud, D.; Perouty, P.; Charlot, M.

    2005-12-01

    Spent nuclear fuel reprocessing to recover energy-producing elements such as uranium or plutonium can be performed by a pyrochemical process. In such method, the actinides and fission products are extracted by electrodeposition in a molten chloride medium. These processes generate chlorinated alkali salt flows contaminated by fission products, mainly Cs, Ba, Sr and rare earth elements constituting high-level waste. Two possible alternatives are investigated for managing this wasteform; a protocol is described for dechlorinating the fission products to allow vitrification, and mineral phases capable of immobilizing chlorides are listed to allow specification of a dedicated ceramic matrix suitable for containment of these chlorinated waste streams. The results of tests to synthesize chlorosilicate phases are also discussed.

  6. Diffusion of fission products and radiation damage in SiC

    NASA Astrophysics Data System (ADS)

    Malherbe, Johan B.

    2013-11-01

    A major problem with most of the present nuclear reactors is their safety in terms of the release of radioactivity into the environment during accidents. In some of the future nuclear reactor designs, i.e. Generation IV reactors, the fuel is in the form of coated spherical particles, i.e. TRISO (acronym for triple coated isotropic) particles. The main function of these coating layers is to act as diffusion barriers for radioactive fission products, thereby keeping these fission products within the fuel particles, even under accident conditions. The most important coating layer is composed of polycrystalline 3C-SiC. This paper reviews the diffusion of the important fission products (silver, caesium, iodine and strontium) in SiC. Because radiation damage can induce and enhance diffusion, the paper also briefly reviews damage created by energetic neutrons and ions at elevated temperatures, i.e. the temperatures at which the modern reactors will operate, and the annealing of the damage. The interaction between SiC and some fission products (such as Pd and I) is also briefly discussed. As shown, one of the key advantages of SiC is its radiation hardness at elevated temperatures, i.e. SiC is not amorphized by neutrons or bombardment at substrate temperatures above 350 °C. Based on the diffusion coefficients of the fission products considered, the review shows that at the normal operating temperatures of these new reactors (i.e. less than 950 °C) the SiC coating layer is a good diffusion barrier for these fission products. However, at higher temperatures the design of the coated particles needs to be adapted, possibly by adding a thin layer of ZrC.

  7. Post-irradiation Examination and Fission Product Inventory Analysis of AGR-1 Irradiation Capsules

    SciTech Connect

    J M Harp; P D Demkowicz; S A Ploger

    2012-10-01

    The AGR-1 experiment was the first in a series of Advanced Gas Reactor (AGR) experiments designed to test TRISO fuel under High Temperature Gas Reactor irradiation conditions. This experiment was irradiated in the Advanced Test Reactor (ATR) at Idaho National Laboratory (INL) and is currently undergoing post-irradiation examination (PIE) at INL’s Materials and Fuels Complex (MFC). The inventory and distribution of fission products, especially Ag-110m, was assessed and analyzed for all the components of the AGR-1 capsules. This data should help inform the study of fission product migration in coated particle fuel. Gamma spectrometry was used to measure the activity of various different fission products in the different components of the AGR-1 test train. Each capsule contained: 12 fuel compacts, a graphite holder that kept the fuel compacts in place, graphite spacers that were above and below the graphite holders and fuel compacts, gas lines through which a helium neon gas mixture flowed in and out of each capsule, and the stainless steel shell that contained the experiment. Gamma spectrometry results and the experimental techniques used to capture these results will be presented for all the capsule components. The components were assayed to determine the total activity of different fission products present in or on them. These totals are compared to the total expected activity of a particular fission product in the capsule based on predictions from physics simulation. Based on this metric, a significant fraction of the Ag-110m was detected outside the fuel compacts, but the amount varied highly between the 6 capsules. Very small fractions of Cs-137 (<2E-5), Cs-134 (<1e-5), and Eu-154 (<4e-4) were detected outside of the fuel compacts. Additionally, the distribution of select fission products in some of the components including the fuel compacts and the graphite holders were measured and will be discussed.

  8. Chemical forms of solid fission products in the irradiated uranium—plutonium mixed nitride fuel

    NASA Astrophysics Data System (ADS)

    Arai, Yasuo; Maeda, Atsushi; Shiozawa, Ken-ichi; Ohmichi, Toshihiko

    1994-06-01

    Chemical forms of solid fission products in the irradiated (U, Pu)N fuel were estimated by both thermodynamic equilibrium calculation and electron microprobe analysis on burnup simulated samples prepared by carbothermic reduction. Besides the MX type matrix phase dissolving zirconium, niobium, yttrium and rare earth elements, the existence of two kinds of inclusion was recognized. One is URu 3 type intermetallic compound constituted by uranium and platinum group elements. The other is an alloy containing molybdenum as a principal constituent. Furthermore, the swelling rate due to solid fission products precipitation was evaluated to be about 0.5% per %FIMA.

  9. Integral data testing of ENDF/B fission-product data and comparisons of ENDF/B with other fission product data files

    SciTech Connect

    LaBauve, R.J.; England, T.R.; George, D.C.

    1981-11-01

    Three experiments (one from Oak Ridge and two from Los Alamos), in which samples of /sup 235/U and /sup 238/Pu were irradiated with thermal neutrons and either the total, gamma-ray, or gamma- and beta-ray fission product decay-energies were measured as functions of cooling time, were selected for comparisons with calculations made using four different fission product data files. The data files used were (1) the ENDF/B-IV fission product file, (2) the ENDF/B-V fission product file, (3) a file derived by substituting decay energies from JNDC into the ENDF/B-V file, and (4) a file derived by substituting decay-energies and spectra from the UK data file into the ENDF/B-V file. Direct summation calculations and spectral comparisons of the experiments were made using these data files as input, and both types of calculational analyses yielded the same results; namely, all data files are deficient, but the JNDC-ENDF/B-V results for the gamma- and beta-ray total decay-energy agree best with experiments. In addition, spectral comparisons with experiment generally indicate that calculated gamma-ray decay-energies are relatively high for early cooling times and small gamma-ray energies; they are low for early cooling times and large gamma-ray energies. The opposite is somewhat the case for the beta-ray decay energies; that is, the calculations are generally low for small beta-ray energies and high for large energies.

  10. Integrated separation scheme for measuring a suite of fission and activation products from a fresh mixed fission and activation product sample

    SciTech Connect

    Morley, Shannon M.; Seiner, Brienne N.; Finn, Erin C.; Greenwood, Lawrence R.; Smith, Steven C.; Gregory, Stephanie J.; Haney, Morgan M.; Lucas, Dawn D.; Arrigo, Leah M.; Beacham, Tere A.; Swearingen, Kevin J.; Friese, Judah I.; Douglas, Matthew; Metz, Lori A.

    2015-05-01

    Mixed fission and activation materials resulting from various nuclear processes and events contain a wide range of isotopes for analysis spanning almost the entire periodic table. In some applications such as environmental monitoring, nuclear waste management, and national security a very limited amount of material is available for analysis and characterization so an integrated analysis scheme is needed to measure multiple radionuclides from one sample. This work describes the production of a complex synthetic sample containing fission products, activation products, and irradiated soil and determines the percent recovery of select isotopes through the integrated chemical separation scheme. Results were determined using gamma energy analysis of separated fractions and demonstrate high yields of Ag (76 ± 6%), Au (94 ± 7%), Cd (59 ± 2%), Co (93 ± 5%), Cs (88 ± 3%), Fe (62 ± 1%), Mn (70 ± 7%), Np (65 ± 5%), Sr (73 ± 2%) and Zn (72 ± 3%). Lower yields (< 25%) were measured for Ga, Ir, Sc, and W. Based on the results of this experiment, a complex synthetic sample can be prepared with low atom/fission ratios and isotopes of interest accurately and precisely measured following an integrated chemical separation method.

  11. Method of fission product beta spectra measurements for predicting reactor anti-neutrino emission

    SciTech Connect

    Asner, David M.; Burns, Kimberly A.; Campbell, Luke W.; Greenfield, Bryce A.; Kos, Marek S.; Orrell, John L.; Schram, Malachi; VanDevender, Brent A.; Wood, Lynn S.; Wootan, David W.

    2015-03-01

    The nuclear fission process that occurs in the core of nuclear reactors results in unstable, neutron-rich fission products that subsequently beta decay and emit electron antineutrinos. These reactor neutrinos have served neutrino physics research from the initial discovery of the neutrino to today's precision measurements of neutrino mixing angles. The prediction of the absolute flux and energy spectrum of the emitted reactor neutrinos hinges upon a series of seminal papers based on measurements performed in the 1970s and 1980s. The steadily improving reactor neutrino measurement techniques and recent reconsiderations of the agreement between the predicted and observed reactor neutrino flux motivates revisiting the underlying beta spectra measurements. A method is proposed to use an accelerator proton beam delivered to an engineered target to yield a neutron field tailored to reproduce the neutron energy spectrum present in the core of an operating nuclear reactor. Foils of the primary reactor fissionable isotopes placed in this tailored neutron flux will ultimately emit beta particles from the resultant fission products. Measurement of these beta particles in a time projection chamber with a perpendicular magnetic field provides a distinctive set of systematic considerations for comparison to the original seminal beta spectra measurements. Ancillary measurements such as gamma-ray emission and post-irradiation radiochemical analysis will further constrain the absolute normalization of beta emissions per fission. The requirements for unfolding the beta spectra measured with this method into a predicted reactor neutrino spectrum are explored.

  12. Fission Product Yields from 232Th, 238U, and 235U Using 14 MeV Neutrons

    NASA Astrophysics Data System (ADS)

    Pierson, B. D.; Greenwood, L. R.; Flaska, M.; Pozzi, S. A.

    2017-01-01

    Neutron-induced fission yield studies using deuterium-tritium fusion-produced 14 MeV neutrons have not yet directly measured fission yields from fission products with half-lives on the order of seconds (far from the line of nuclear stability). Fundamental data of this nature are important for improving and validating the current models of the nuclear fission process. Cyclic neutron activation analysis (CNAA) was performed on three actinide targets-thorium-oxide, depleted uranium metal, and highly enriched uranium metal-at the University of Michigan's Neutron Science Laboratory (UM-NSL) using a pneumatic system and Thermo-Scientific D711 accelerator-based fusion neutron generator. This was done to measure the fission yields of short-lived fission products and to examine the differences between the delayed fission product signatures of the three actinides. The measured data were compared against previously published results for 89Kr, -90, and -92 and 138Xe, -139, and -140. The average percent deviation of the measured values from the Evaluated Nuclear Data Files VII.1 (ENDF/B-VII.1) for thorium, depleted-uranium, and highly-enriched uranium were -10.2%, 4.5%, and -12.9%, respectively. In addition to the measurements of the six known fission products, 23 new fission yield measurements from 84As to 146La are presented.

  13. Gaseous fission product management for molten salt reactors and vented fuel systems

    SciTech Connect

    Messenger, S. J.; Forsberg, C.; Massie, M.

    2012-07-01

    Fission gas disposal is one of the unresolved difficulties for Molten Salt Reactors (MSRs) and advanced reactors with vented fuel systems. As these systems operate, they produce many radioactive isotopes of xenon and krypton (e.g. {sup 135}Xe t{sub 1/2} = 9.14 hours and {sup 85}Kr t{sub 1/2}= 10.73 years). Removing these gases proves vital to the success of such reactor designs for two reasons. First, the gases act as large neutron sinks which decrease reactivity and must be counterbalanced by increasing fuel loading. Second, for MSRs, inert fission product gases naturally separate quickly from high temperature salts, thus creating high vapor pressure which poses safety concerns. For advanced reactors with solid vented fuel, the gases are allowed to escape into an off-gas system and thus must be managed. Because of time delays in transport of fission product gases in vented fuel systems, some of the shorter-lived radionuclides will decay away thereby reducing the fission gas source term relative to an MSR. To calculate the fission gas source term of a typical molten salt reactor, we modeled a 1000 MWe graphite moderated thorium MSR similar to that detailed in Mathieu et al. [1]. The fuel salt used in these calculations was LiF (78 mole percent) - (HN)F 4 (22 mole percent) with a heavy nuclide composition of 3.86% {sup 233}U and 96.14% {sup 232}Th by mass. Before we can remove the fission product gases produced by this reactor configuration, we must first develop an appropriate storage mechanism. The gases could be stored in pressurized containers but then one must be concerned about bottle failure. Methods to trap noble gases in matrices are expensive and complex. Alternatively, there are direct storage/disposal options: direct injection into the Earth or injecting a grout-based product into the Earth. Advances in drilling technologies, hydro fracture technologies, and methods for the sequestration of carbon dioxide from fossil fuel plants are creating new options

  14. Relative yields of U-235 fission products measured in a high level radioactive sludge at Savannah River Site

    SciTech Connect

    Bibler, N.E.; Coleman, C.J.; Kinard, W.F.

    1992-10-01

    This paper presents measurements of the concentrations of 42 of the long-lived U-235 fission products in a high-level radioactive waste sludge stored at Savannah River Site. The 42 fision products make up 98% of the waste sludge. We used inductively coupled plasma-mass spectroscopy for the analysis. The relative yields for most of the fission products are in complete agreement with the known relative yields for the beta decay chains of the two asymmetric branches of the slow neutron fission of U-235. Disagreements can be reconciled based on the chemistry of the fission products in the caustic waste sludges, the neutron fluences in SRS reactors, or interferences in the ICP-MS analyses. This paper presents measurements of the concentrations of 42 (98%) of the long-lived U-235 fission products in a high-level radioactive waste sludge stored at the Savannah River Site. We analyzed the sludge with inductively coupled plasma-mass spectroscopy. The relative yields for most of the fission products agree completely with the known relative vields for the beta decay chains of the two asymmetric: branches of the slow neutron fission of U-235. The chemistry of the fission products in the caustic waste sludges, the neutron fluences in SRS reactors, or interferences in the ICP-MS analyses explain the differences in the measured and calculated results.

  15. Relative yields of U-235 fission products measured in a high level radioactive sludge at Savannah River Site

    SciTech Connect

    Bibler, N.E.; Coleman, C.J. ); Kinard, W.F. . Dept. of Chemistry)

    1992-01-01

    This paper presents measurements of the concentrations of 42 of the long-lived U-235 fission products in a high-level radioactive waste sludge stored at Savannah River Site. The 42 fision products make up 98% of the waste sludge. We used inductively coupled plasma-mass spectroscopy for the analysis. The relative yields for most of the fission products are in complete agreement with the known relative yields for the beta decay chains of the two asymmetric branches of the slow neutron fission of U-235. Disagreements can be reconciled based on the chemistry of the fission products in the caustic waste sludges, the neutron fluences in SRS reactors, or interferences in the ICP-MS analyses. This paper presents measurements of the concentrations of 42 (98%) of the long-lived U-235 fission products in a high-level radioactive waste sludge stored at the Savannah River Site. We analyzed the sludge with inductively coupled plasma-mass spectroscopy. The relative yields for most of the fission products agree completely with the known relative vields for the beta decay chains of the two asymmetric: branches of the slow neutron fission of U-235. The chemistry of the fission products in the caustic waste sludges, the neutron fluences in SRS reactors, or interferences in the ICP-MS analyses explain the differences in the measured and calculated results.

  16. Study on collection efficiency of fission products by spray: Experimental device and modelling

    SciTech Connect

    Ducret, D.; Roblot, D.; Vendel, J.; Billarand, Y.

    1997-08-01

    Consequences of an hypothetical overheating reactor accident in nuclear power plants can be limited by spraying cold water drops into containment building. The spray reduces the pressure and the temperature levels by condensation of steam and leads to the washout of fission products (aerosols and gaseous iodine). The present study includes a large program devoted to the evaluation of realistic washout rates. An experimental device (named CARAIDAS) was designed and built in order to determine the collection efficiency of aerosols and iodine absorption by drops with representative conditions of post-accident atmosphere. This experimental device is presented in the paper and more particularly: (1) the experimental enclosure in which representative thermodynamic conditions can be achieved, (2) the monosized drops generator, the drops diameter measurement and the drops collector, (3) the cesium iodide aerosols generator and the aerosols measurements. Modelling of steam condensation on drops aerosols collection and iodine absorption are described. First experimental and code results on drops and aerosols behaviour are compared. 8 refs., 18 figs.

  17. Measurements of isomeric yield ratios of fission products from proton-induced fission on natU and 232Th via direct ion counting

    NASA Astrophysics Data System (ADS)

    Rakopoulos, Vasileios; Lantz, Mattias; Al-Adili, Ali; Gorelov, Dmitry; Jokinen, Ari; Kolhinen, Veli; Mattera, Andrea; Moore, Iain D.; Penttilä, Heikki; Prokofiev, Alexander V.; Solders, Andreas; Pomp, Stephan

    2017-09-01

    Independent isomeric yield ratios (IYR) of 81Ge, 96Y, 97Y, 97Nb, 128Sn and 130Sn have been determined in the 25 MeV proton-induced fission of natU and 232Th. The measurements were performed at the Ion Guide Isotope Separator On-Line (IGISOL) facility at the University of Jyväskylä. A direct ion counting measurement of the isomeric fission yield ratios was accomplished for the first time, registering the fission products in less than a second after their production. In addition, the IYRs of natU were measured by means of γ-spectroscopy in order to verify the consistency of the recently upgraded experimental setup. From the obtained results, indications of a dependence of the production rate on the fissioning system can be noticed. These data were compared with data available in the literature, whenever possible. Using the TALYS code and the experimentally obtained IYRs, we also deduced the average angular momentum of the fission fragments after scission.

  18. Production of fissioning uranium plasma to approximate gas-core reactor conditions

    NASA Technical Reports Server (NTRS)

    Lee, J. H.; Mcfarland, D. R.; Hohl, F.; Kim, K. H.

    1974-01-01

    The intense burst of neutrons from the d-d reaction in a plasma-focus apparatus is exploited to produce a fissioning uranium plasma. The plasma-focus apparatus consists of a pair of coaxial electrodes and is energized by a 25 kJ capacitor bank. A 15-g rod of 93% enriched U-235 is placed in the end of the center electrode where an intense electron beam impinges during the plasma-focus formation. The resulting uranium plasma is heated to about 5 eV. Fission reactions are induced in the uranium plasma by neutrons from the d-d reaction which were moderated by the polyethylene walls. The fission yield is determined by evaluating the gamma peaks of I-134, Cs-138, and other fission products, and it is found that more than 1,000,000 fissions are induced in the uranium for each focus formation, with at least 1% of these occurring in the uranium plasma.

  19. US/UK actinides experiment at the Dounreay PFR. 1: Fission products

    SciTech Connect

    Raman, S.; Murphy, B.D.

    1995-09-01

    The US and the United Kingdom have been engaged in a joint research program in which samples of higher actinides were irradiated in the 600-MW Dounreay Prototype Fast Reactor in Scotland. Analytical results using mass spectrometry and radiometry for actinides and fission products are now available for the samples in Fuel Pins 1 and 2 which were irradiated for 63 full-power days and for the samples in Fuel Pin 4 which were irradiated for 492 full-power days. Results from these three fuel pins are providing estimates of integral cross sections and fission yields.

  20. SEPARATION OF FISSION PRODUCT VALUES FROM THE HEXAVALENT PLUTONIUM BY CARRIER PRECIPITATION

    DOEpatents

    Davies, T.H.

    1959-12-15

    An improved precipitation of fission products on bismuth phosphate from an aqueous mineral acid solution also containing hexavalent plutonium by incorporating, prior to bismuth phosphate precipitation, from 0.05 to 2.5 grams/ liter of zirconium phosphate, niobium oxide. and/or lanthanum fluoride is described. The plutonium remains in solution.

  1. Report on the Behavior of Fission Products in the Co-decontamination Process

    SciTech Connect

    Martin, Leigh Robert; Riddle, Catherine Lynn

    2015-09-30

    This document was prepared to meet FCT level 3 milestone M3FT-15IN0302042, “Generate Zr, Ru, Mo and Tc data for the Co-decontamination Process.” This work was carried out under the auspices of the Lab-Scale Testing of Reference Processes FCT work package. This document reports preliminary work in identifying the behavior of important fission products in a Co-decontamination flowsheet. Current results show that Tc, in the presence of Zr alone, does not behave as the Argonne Model for Universal Solvent Extraction (AMUSE) code would predict. The Tc distribution is reproducibly lower than predicted, with Zr distributions remaining close to the AMUSE code prediction. In addition, it appears there may be an intricate relationship between multiple fission product metals, in different combinations, that will have a direct impact on U, Tc and other important fission products such as Zr, Mo, and Rh. More extensive testing is required to adequately predict flowsheet behavior for these variances within the fission products.

  2. Influence of radiation on formation of fission product aerosols during LWR degraded core accidents

    SciTech Connect

    Chuang, C.F.; Im, K.H.; Ahluwalia, R.K.

    1984-01-01

    Purpose of this paper is to construct a model for estimating the number density of ions produced by the high radiation levels in reactor core and upper plenum and to use this estimate to determine the effect of ions on the formation of fission product aerosols.

  3. Fission product behavior in the Peach Bottom and Fort St. Vrain HTGRs

    SciTech Connect

    Hanson, D.L.; Baldwin, N.L.; Strong, D.E.

    1980-11-01

    Actual operating data from Peach Bottom and Fort St. Vrain were compared with code predictions to assess the validity of the methods used to predict the behavior of fission products in the primary coolant circuit. For both reactors the measured circuit activities were significantly below design values, and the observations generally verify the codes used for large HTGR design.

  4. Comparison of fission product release predictions using PARFUME with results from the AGR-1 irradiation experiment

    SciTech Connect

    Blaise Collin

    2014-09-01

    This report documents comparisons between post-irradiation examination measurements and model predictions of silver (Ag), cesium (Cs), and strontium (Sr) release from selected tristructural isotropic (TRISO) fuel particles and compacts during the first irradiation test of the Advanced Gas Reactor program that occurred from December 2006 to November 2009 in the Advanced Test Reactor (ATR) at Idaho National Laboratory (INL). The modeling was performed using the particle fuel model computer code PARFUME (PARticle FUel ModEl) developed at INL. PARFUME is an advanced gas-cooled reactor fuel performance modeling and analysis code (Miller 2009). It has been developed as an integrated mechanistic code that evaluates the thermal, mechanical, and physico-chemical behavior of fuel particles during irradiation to determine the failure probability of a population of fuel particles given the particle-to-particle statistical variations in physical dimensions and material properties that arise from the fuel fabrication process, accounting for all viable mechanisms that can lead to particle failure. The code also determines the diffusion of fission products from the fuel through the particle coating layers, and through the fuel matrix to the coolant boundary. The subsequent release of fission products is calculated at the compact level (release of fission products from the compact) but it can be assessed at the particle level by adjusting the diffusivity in the fuel matrix to very high values. Furthermore, the diffusivity of each layer can be individually set to a high value (typically 10-6 m2/s) to simulate a failed layer with no capability of fission product retention. In this study, the comparison to PIE focused on fission product release and because of the lack of failure in the irradiation, the probability of particle failure was not calculated. During the AGR-1 irradiation campaign, the fuel kernel produced and released fission products, which migrated through the successive

  5. Exploratory study of fission product yield determination from photofission of Pu239 at 11 MeV with monoenergetic photons

    DOE PAGES

    Bhike, Megha; Tornow, W.; Krishichayan, -; ...

    2017-02-14

    Here, measurements of fission product yields play an important role for the understanding of fundamental aspects of the fission process. Recently, neutron-induced fission product-yield data of 239Pu at energies below 4 MeV revealed an unexpected energy dependence of certain fission fragments. In order to investigate whether this observation is prerogative to neutron-induced fission, a program has been initiated to measure fission product yields in photoinduced fission. Here we report on the first ever photofission product yield measurement with monoenergetic photons produced by Compton back-scattering of FEL photons. The experiment was performed at the High-Intensity Gamma-ray Source at Triangle Universities Nuclear Laboratory on 239Pu at Eγmore » = 11 MeV. In this exploratory study the yield of eight fission products ranging from 91Sr to 143Ce has been obtained.« less

  6. Mechanistic approach for nitride fuel evolution and fission product release under irradiation

    NASA Astrophysics Data System (ADS)

    Dolgodvorov, A. P.; Ozrin, V. D.

    2017-01-01

    A model for describing uranium-plutonium mixed nitride fuel pellet burning was developed. Except fission products generating, the model includes impurities of oxygen and carbon. Nitrogen behaviour in nitride fuel was analysed and the nitrogen chemical potential in solid solution with uranium-plutonium nitride was constructed. The chemical program module was tested with the help of thermodynamic equilibrium phase distribution calculation. Results were compared with analogous data in literature, quite good agreement was achieved, especially for uranium sesquinitride, metallic species and some oxides. Calculation of a process of nitride fuel burning was also conducted. Used mechanistic approaches for fission product evolution give the opportunity to find fission gas release fractions and also volumes of intergranular secondary phases. Calculations present that the most massive secondary phases are the oxide and metallic phases. Oxide phase contain approximately 1 % wt of substance over all time of burning with slightly increasing of content. Metallic phase has considerable rising of mass and by the last stage of burning it contains about 0.6 % wt of substance. Intermetallic phase has less increasing rate than metallic phase and include from 0.1 to 0.2 % wt over all time of burning. The highest element fractions of released gaseous fission products correspond to caesium and iodide.

  7. Fission Product Inventory and Burnup Evaluation of the AGR-2 Irradiation by Gamma Spectrometry

    SciTech Connect

    Harp, Jason M.; Demkowicz, Paul A.; Stempien, John D.

    2016-11-01

    Gamma spectrometry has been used to evaluate the burnup and fission product inventory of different components from the US Advanced Gas Reactor Fuel Development and Qualification Program's second TRISO-coated particle fuel irradiation test (AGR-2). TRISO fuel in this irradiation included both uranium carbide / uranium oxide (UCO) kernels and uranium oxide (UO2) kernels. Four of the 6 capsules contained fuel from the US Advanced Gas Reactor program, and only those capsules will be discussed in this work. The inventories of gamma-emitting fission products from the fuel compacts, graphite compact holders, graphite spacers and test capsule shell were evaluated. These data were used to measure the fractional release of fission products such as Cs-137, Cs-134, Eu-154, Ce-144, and Ag-110m from the compacts. The fraction of Ag-110m retained in the compacts ranged from 1.8% to full retention. Additionally, the activities of the radioactive cesium isotopes (Cs-134 and Cs-137) have been used to evaluate the burnup of all US TRISO fuel compacts in the irradiation. The experimental burnup evaluations compare favorably with burnups predicted from physics simulations. Predicted burnups for UCO compacts range from 7.26 to 13.15 % fission per initial metal atom (FIMA) and 9.01 to 10.69 % FIMA for UO2 compacts. Measured burnup ranged from 7.3 to 13.1 % FIMA for UCO compacts and 8.5 to 10.6 % FIMA for UO2 compacts. Results from gamma emission computed tomography performed on compacts and graphite holders that reveal the distribution of different fission products in a component will also be discussed. Gamma tomography of graphite holders was also used to locate the position of TRISO fuel particles suspected of having silicon carbide layer failures that lead to in-pile cesium release.

  8. Fission Product Inventory and Burnup Evaluation of the AGR-2 Irradiation by Gamma Spectrometry

    SciTech Connect

    Harp, Jason Michael; Stempien, John Dennis; Demkowicz, Paul Andrew

    2016-09-01

    Gamma spectrometry has been used to evaluate the burnup and fission product inventory of different components from the US Advanced Gas Reactor Fuel Development and Qualification Program's second TRISO-coated particle fuel irradiation test (AGR-2). TRISO fuel in this irradiation included both uranium carbide / uranium oxide (UCO) kernels and uranium oxide (UO2) kernels. Four of the 6 capsules contained fuel from the US Advanced Gas Reactor program, and only those capsules will be discussed in this work. The inventories of gamma-emitting fission products from the fuel compacts, graphite compact holders, graphite spacers and test capsule shell were evaluated. These data were used to measure the fractional release of fission products such as Cs-137, Cs-134, Eu-154, Ce-144, and Ag-110m from the compacts. The fraction of Ag-110m retained in the compacts ranged from 1.8% to full retention. Additionally, the activities of the radioactive cesium isotopes (Cs-134 and Cs-137) have been used to evaluate the burnup of all US TRISO fuel compacts in the irradiation. The experimental burnup evaluations compare favorably with burnups predicted from physics simulations. Predicted burnups for UCO compacts range from 7.26 to 13.15 % fission per initial metal atom (FIMA) and 9.01 to 10.69 % FIMA for UO2 compacts. Measured burnup ranged from 7.3 to 13.1 % FIMA for UCO compacts and 8.5 to 10.6 % FIMA for UO2 compacts. Results from gamma emission computed tomography performed on compacts and graphite holders that reveal the distribution of different fission products in a component will also be discussed. Gamma tomography of graphite holders was also used to locate the position of TRISO fuel particles suspected of having silicon carbide layer failures that lead to in-pile cesium release.

  9. Mass yield distributions of fission products from photo-fission of 238U induced by 11.5-17.3 MeV bremsstrahlung

    NASA Astrophysics Data System (ADS)

    Naik, H.; Carrel, Frédérick; Kim, G. N.; Laine, Frédéric; Sari, Adrien; Normand, S.; Goswami, A.

    2013-07-01

    The yields of various fission products in the 11.5, 13.4, 15.0 and 17.3 MeV bremsstrahlung-induced fission of 238U have been determined by recoil catcher and an off-line γ-ray spectrometric technique using the electron linac, SAPHIR at CEA, Saclay, France. The mass yield distributions were obtained from the fission product yields using charge-distribution corrections. The peak-to-valley ( P/ V ratio, average light mass (< A L>) and heavy mass (< A H>) and average number of neutrons (< v>) in the bremsstrahlung-induced fission of 238U at different excitation energies were obtained from the mass yield data. From the present and literature data in the 238U ( γ, f ) and 238U ( n, f ) reactions at various energies, the following observations were obtained: i) The mass yield distributions in the 238U ( γ, f ) reaction at various energies of the present work are double-humped, similar to those of the 238U ( n, f ) reaction of comparable excitation energy. ii) The yields of fission products for A = 133-134, A = 138-140, and A = 143-144 and their complementary products in the 238U ( γ, f) reaction are higher than other fission products due to the nuclear structure effect. iii) The yields of fission products for A = 133-134 and their complementary products are slightly higher in the 238U ( γ, f ) than in the 238U ( n, f ) , whereas for A = 138-140 and 143-144 and their complementary products are comparable. iv) With excitation energy, the increase of yields of symmetric products and the decrease of the peak-to-valley ( P/ V ratio in the 238U ( γ, f) reaction is similar to the 238U ( n, f) reaction. v) The increase of < v> with excitation energy is also similar between the 238U ( γ, f ) and 238U ( n, f) reactions. However, it is surprising to see that the < A L> and < A H> values with excitation energy behave entirely differently from the 238U ( γ, f ) and 238U ( n, f ) reactions.

  10. Grain boundary sweeping and dissolution effects on fission product behavior under severe fuel damage accident conditions

    SciTech Connect

    Rest, J.

    1985-10-01

    The theoretical FASTGRASS-VFP model has been used in the interpretation of fission gas, iodine, tellurium, and cesium release from severe-fuel-damage (SFD) tests performed in the PBF reactor in Idaho. A theory of grain boundary sweeping of gas bubbles, gas bubble behavior during fuel liquefaction (destruction of grain boundaries due to formation of a U-rich melt phase), and during U-Zr eutectic melting has been included within the FASTGRASS-VFP formalism. The grain-boundary-sweeping theory considers the interaction between the moving grain boundary and two distinct size classes of bubbles, those on grain faces and on grain edges. The theory of the effects of fuel liquefaction and U-Zr eutectic melting on fission product behavior considers the migration and coalescence of fission gas bubbles in either molten uranium, or a zircaloy-uranium eutectic melt. The FASTGRASS-VFP predictions, measured release rates from the above tests, and previously published release rates are compared and differences between fission product behavior in trace-irradiated and in normally irradiated fuel are highlighted.

  11. REMOVAL OF CERTAIN FISSION PRODUCT METALS FROM LIQUID BISMUTH COMPOSITIONS

    DOEpatents

    Dwyer, O.E.; Howe, H.E.; Avrutik, E.R.

    1959-11-24

    A method is described for purifying a solution of urarium in liquid bismuth containing at least one metal from the group consisting of selenium, tellurium, palladium, ruthenium, rhodium, niobium, and zirconium. The solution is contacted with zinc in an inert atmosphere to form a homogeneous melt, a solid zinc phase is formed, and the zinc phase containing the metal is separated from the melt.

  12. Charge distribution of light mass fission products in the fast neutron induced fission of (232)Th, (238)U, (240)Pu and (244)Cm.

    PubMed

    Naik, Haladhara; Singh, Ram Janam; Dange, Shrikant Pandurang

    2017-09-01

    Fractional cumulative yields (FCY) of various light mass fission products in the fast neutron induced fission of (232)Th, (238)U, (240)Pu and (244)Cm have been determined by using the off-line γ-ray spectrometric technique. From present and literature data, width of isobaric charge distribution (σZ), the most probable charge (ZP) and the experimental charge polarization (∆ΖEXPT) as a function of fragment mass were deduced. The ∆ΖEXPT values from the present work for light mass chains and earlier work for heavy mass chains show oscillating nature due to nuclear structure effect. The ∆ΖMPE values based on minimum potential energy surface were theoretically calculated, which shows a systematic decrease trend with the approach of symmetric split due to the liquid drop behaviour of the fissioning nucleus. Copyright © 2017 Elsevier Ltd. All rights reserved.

  13. FITPULS: a code for obtaining analytic fits to aggregate fission-product decay-energy spectra. [In FORTRAN

    SciTech Connect

    LaBauve, R.J.; George, D.C.; England, T.R.

    1980-03-01

    The operation and input to the FITPULS code, recently updated to utilize interactive graphics, are described. The code is designed to retrieve data from a library containing aggregate fine-group spectra (150 energy groups) from fission products, collapse the data to few groups (up to 25), and fit the resulting spectra along the cooling time axis with a linear combination of exponential functions. Also given in this report are useful results for aggregate gamma and beta spectra from the decay of fission products released from /sup 235/U irradiated with a pulse (10/sup -4/ s irradiation time) of thermal neutrons. These fits are given in 22 energy groups that are the first 22 groups of the LASL 25-group decay-energy group structure, and the data are expressed both as MeV per fission second and particles per fission second; these pulse functions are readily folded into finite fission histories. 65 figures, 11 tables.

  14. Formation and characterization of fission-product aerosols under postulated HTGR accident conditions

    SciTech Connect

    Tang, I.N.; Munkelwitz, H.R.

    1982-07-01

    The paper presents the results of an experimental investigation on the formation mechanism and physical characterization of simulated nuclear aerosols that could likely be released during an HTGR core heat-up accident. Experiments were carried out in a high-temperature flow system consisting essentially of an inductively heated release source, a vapor deposition tube, and a filter assembly for collecting particulate matter. Simulated fission products Sr and Ba as oxides are separately impregnated in H451 graphite wafers and released at elevated temperatures into a dry helium flow. In the presence of graphite, the oxides are quantitatively reduced to metals, which subsequently vaporize at temperatures much lower than required for the oxides alone to vaporize in the absence of graphite. A substantial fraction of the released material is associated with particulate matter, which is collected on filters located downstream at ambient temperature. The release and transport of simulated fission product Ag as metal are also investigated.

  15. Fission product transport and behavior during two postulated loss of flow transients in the air

    SciTech Connect

    Adams, J.P.; Carboneau, M.L.

    1991-01-01

    This document discusses fission product behavior during two postulated loss-of-flow accidents (leading to high- and low-pressure core degradation, respectively) in the Advanced Test Reactor (ATR). These transients are designated ATR Transient LCPI5 (high-pressure) and LPP9 (low-pressure). Normally, transients of this nature would be easily mitigated using existing safety systems and procedures. In these analyses, failure of these safety systems was assumed so that core degradation and fission product release could be analyzed. A probabilistic risk assessment indicated that the probability of occurrence for these two transients is of the order of 10{sup {minus}5 }and 10{sup {minus}7} per reactor year for LCP15 and LPP9, respectively.

  16. Fission product transport and behavior during two postulated loss of flow transients in the air

    SciTech Connect

    Adams, J.P.; Carboneau, M.L.

    1991-12-31

    This document discusses fission product behavior during two postulated loss-of-flow accidents (leading to high- and low-pressure core degradation, respectively) in the Advanced Test Reactor (ATR). These transients are designated ATR Transient LCPI5 (high-pressure) and LPP9 (low-pressure). Normally, transients of this nature would be easily mitigated using existing safety systems and procedures. In these analyses, failure of these safety systems was assumed so that core degradation and fission product release could be analyzed. A probabilistic risk assessment indicated that the probability of occurrence for these two transients is of the order of 10{sup {minus}5 }and 10{sup {minus}7} per reactor year for LCP15 and LPP9, respectively.

  17. Ab initio energetics of some fission products (Kr, I, Cs, Sr and He) in uranium dioxide

    NASA Astrophysics Data System (ADS)

    Crocombette, Jean-Paul

    2002-09-01

    A computational study of some fission products (FP) energetics in uranium dioxide is presented. Krypton, iodine, caesium, strontium and helium are considered. Calculations are made within the density functional theory in the local density approximation with the plane wave pseudopotential method. Three insertion sites are considered: the octahedral interstitial position and the oxygen and uranium substitution sites. The importance of atomic relaxations is estimated on the He and Kr cases. They prove quantitatively important but can be neglected to draw qualitative trends. For each fission product incorporation and solution energies are calculated. The obtained values of the solutions energies of the various FP are in good agreement with their experimental behaviour: Kr, Cs and I atoms are insoluble in uranium dioxide, Sr solubility depends on the stoichiometry of urania. He atoms are found to have little interaction with their environment in uranium doxide.

  18. High-power proton linac for transmuting the long-lived fission products in nuclear waste

    SciTech Connect

    Lawrence, G.P.

    1991-01-01

    High power proton linacs are being considered at Los Alamos as drivers for high-flux spallation neutron sources that can be used to transmute the troublesome long-lived fission products in defense nuclear waste. The transmutation scheme being studied provides a high flux (> 10{sup 16}/cm{sup 2}{minus}s) of thermal neutrons, which efficiently converts fission products to stable or short-lived isotopes. A medium-energy proton linac with an average beam power of about 110 MW can burn the accumulated Tc99 and I129 inventory at the DOE's Hanford Site within 30 years. Preliminary concepts for this machine are described. 3 refs., 5 figs., 2 tabs.

  19. Post irradiation examination of simulated fission product doped hyperstoichiometric mixed oxide fuel pins*1

    NASA Astrophysics Data System (ADS)

    Götzmann, O.; Kleykamp, H.

    1980-03-01

    Two miniature fuel pins containing uranium-plutonium oxide with a hyperstoichiometric oxygen-to-metal ratio and selective fission product elements have been irradiated in the BR 2 reactor at Mol, Belgium, for two reactor cycles (46 days). One of the pins had a niobium metal coating on the inner cladding surface to act as oxygen getter. Both pins were subjected to a detailed examination by ceramography and electronprobe microanalysis. The results have been interpreted in the light of a recently published thermochemical model for the cladding attack. The very different oxygen potential environments in the two pins produced entirely different clad corrosion phenomena probably due to different cladding attack mechanisms. The niobium coating worked well in reducing the oxygen potential. However, there exists a draw back with niobium due to the formation of relatively stable intermetallic phases with noble metal fission products.

  20. 81929 - Fission-Product Separation Based on Room - Temperature Ionic Liquids

    SciTech Connect

    Robin D. Rogers

    2004-12-09

    This project has demonstrated that Sr2+ and Cs+ can be selectively extracted from aqueous solutions into ionic liquids using crown ethers and that unprecedented large distribution coefficients can be achieved for these fission products. The volume of secondary wastes can be significantly minimized with this new separation technology. Through the current EMSP funding, the solvent extraction technology based on ionic liquids has been shown to be viable and can potentially provide the most efficient separation of problematic fission products from high level wastes. The key results from the current funding period are the development of highly selective extraction process for cesium ions based on crown ethers and calixarenes, optimization of selectivities of extractants via systematic change of ionic liquids, and investigation of task-specific ionic liquids incorporating both complexant and solvent characteristics.

  1. SELECTIVE SEPARATION OF URANIUM FROM THORIUM, PROTACTINIUM AND FISSION PRODUCTS BY PEROXIDE DISSOLUTION METHOD

    DOEpatents

    Seaborg, G.T.; Gofman, J.W.; Stoughton, R.W.

    1959-08-18

    A method is described for separating U/sup 233/ from thorium and fission products. The separation is effected by forming a thorium-nitric acid solution of about 3 pH, adding hydrogen peroxide to precipitate uranium and thorium peroxide, treating the peroxides with sodium hydroxide to selectively precipitate the uranium peroxide, and reacting the separated solution with nitric acid to re- precipitate the uranium peroxide.

  2. Fission-Product Separation Based on Room-Temperature Ionic Liquids

    SciTech Connect

    Luo, Huimin; Rogers, Robin D.; Dai, Sheng, Dai; Bonnesen, Peter V.; Buchanan, A. C. III; Hussey, Charles L.

    2003-06-16

    The objectives of this project are (a) to synthesize new ionic liquids tailored for the extractive separation of Cs + and Sr 2+; (b) to select optimum macrocyclic extractants through studies of complexation of fission products with macrocyclic extractants and transport in new extraction systems based on ionic liquids; (c) to develop efficient processes to recycle ionic liquids and crown ethers; and (d) to investigate chemical stabilities of ionic liquids under strong acid, strong base, and high-level-radiation conditions.

  3. Fission-Product Separation Based on Room-Temperature Ionic Liquids

    SciTech Connect

    Luo, Huimin; Hussey, Charles L.

    2005-09-30

    The objectives of this project are (a) to synthesize new ionic liquids tailored for the extractive separation of Cs + and Sr 2+; (b) to select optimum macrocyclic extractants through studies of complexation of fission products with macrocyclic extractants and transport in new extraction systems based on ionic liquids; (c) to develop efficient processes to recycle ionic liquids and crown ethers; and (d) to investigate chemical stabilities of ionic liquids under strong acid, strong base, and high-level-radiation conditions.

  4. ORNL contributions to NRC state of technology report on fission product iodine

    SciTech Connect

    Mynatt, F.R.

    1981-02-01

    This document is comprised of the following: Chapter 4, Fission Product Release from Fuel; Chapter 5b, Aqueous Iodine Chemistry in LWR Accidents; Appendix (App. C), Aerosol Release Calculations; App. 5B4, Redox Reactions of Iodine Species, App. 5B5, Iodine Hydrolysis; App. 5B6, Organic Iodides in Aqueous Systems; and App. 5B7, Radiation Chemistry of Aqueous Iodide Systems. (DLC)

  5. PROCESS FOR SEGREGATING URANIUM FROM PLUTONIUM AND FISSION-PRODUCT CONTAMINATION

    DOEpatents

    Ellison, C.V.; Runion, T.C.

    1961-06-27

    An aqueous nitric acid solution containing uranium, plutonium, and fission product values is contacted with an organic extractant comprised of a trialkyl phosphate and an organic diluent. The relative amounts of trialkyl phosphate and uranium values are controlled to achieve a concentration of uranium values in the organic extractant of at least 0.35 moles uranium per mole of trialkyl phosphate, thereby preferentially extracting uranium values into the organic extractant.

  6. METHOD OF SEPARATING URANIUM, PLUTONIUM AND FISSION PRODUCTS BY BROMINATION AND DISTILLATION

    DOEpatents

    Jaffey, A.H.; Seaborg, G.T.

    1958-12-23

    The method for separation of plutonium from uranium and radioactive fission products obtained by neutron irradiation of uranlum consists of reacting the lrradiated material with either bromine, hydrogen bromide, alumlnum bromide, or sulfur and bromine at an elevated temperature to form the bromides of all the elements, then recovering substantlally pure plutonium bromide by dlstillatlon in combinatlon with selective condensatlon at prescribed temperature and pressure.

  7. Fission Product Separation from Pyrochemical Electrolyte by Cold Finger Melt Crystallization

    SciTech Connect

    Versey, Joshua R.

    2013-08-01

    This work contributes to the development of pyroprocessing technology as an economically viable means of separating used nuclear fuel from fission products and cladding materials. Electrolytic oxide reduction is used as a head-end step before electrorefining to reduce oxide fuel to metallic form. The electrolytic medium used in this technique is molten LiCl-Li2O. Groups I and II fission products, such as cesium (Cs) and strontium (Sr), have been shown to partition from the fuel into the molten LiCl-Li2O. Various approaches of separating these fission products from the salt have been investigated by different research groups. One promising approach is based on a layer crystallization method studied at the Korea Atomic Energy Research Institute (KAERI). Despite successful demonstration of this basic approach, there are questions that remain, especially concerning the development of economical and scalable operating parameters based on a comprehensive understanding of heat and mass transfer. This research explores these parameters through a series of experiments in which LiCl is purified, by concentrating CsCl in a liquid phase as purified LiCl is crystallized and removed via an argon-cooled cold finger.

  8. Reactive transport modelling of the interaction of fission product ground contamination with alkaline and cementitious leachates

    SciTech Connect

    Kwong, S.; Small, J.

    2007-07-01

    The fission products Cs-137 and Sr-90 are amongst the most common radionuclides occurring in ground contamination at the UK civil nuclear sites. Such contamination is often associated with alkaline liquids and the mobility of these fission products may be affected by these chemical conditions. Similar geochemical effects may also result from cementitious leachate associated with building foundations and the use of grouts to remediate ground contamination. The behaviour of fission products in these scenarios is a complex interaction of hydrogeological and geochemical processes. A suite of modelling tools have been developed to investigate the behaviour of a radioactive plume containing Cs and Sr. Firstly the effects of sorption due to cementitious groundwater is modelled using PHREEQC. This chemical model is then incorporated into PHAST for the 3-D reactive solute transport modeling. Results are presented for a generic scenario including features and processes that are likely to be relevant to a number of civil UK nuclear sites. Initial results show that modelling can be a very cost-effective means to study the complex hydrogeological and geochemical processes involved. Modelling can help predict the mobility of contaminants in a range of site end point scenarios, and in assessing the consequences of decommissioning activities. (authors)

  9. Comparisons of Neutron Cross Sections and Isotopic Composition Calculations for Fission-Product Evaluations

    NASA Astrophysics Data System (ADS)

    Kim, Do Heon; Gil, Choong-Sup; Chang, Jonghwa; Lee, Yong-Deok

    2005-05-01

    The neutron absorption cross sections for 18 fission products evaluated within the framework of the KAERI (Korea Atomic Energy Research Institute)-BNL (Brookhaven National Laboratory) international collaboration have been compared with ENDF/B-VI.7. Also, the influence of the new evaluations on the isotopic composition calculations of the fission products has been estimated through the OECD/NEA burnup credit criticality benchmarks (Phase 1B) and the LWR/Pu recycling benchmarks. These calculations were performed by WIMSD-5B with the 69-group libraries prepared from three evaluated nuclear data libraries: ENDF/B-VI.7, ENDF/B-VI.8 including the new evaluations in the resonance region covering the thermal region, and the expected ENDF/B-VII including those in the upper resonance region up to 20 MeV. For Xe-131, the composition calculated with ENDF/B-VI.8 shows a maximum difference of 5.02% compared to ENDF/B-VI.7. However, the isotopic compositions of all the fission products calculated with the expected ENDF/B-VII show no differences when compared to ENDF/B-VI.7 for the thermal reactor benchmark cases.

  10. Analysis of fission product revaporization in a BWR Reactor Coolant System during a station blackout accident

    SciTech Connect

    Yang, J.W.; Schmidt, E.; Cazzoli, E.; Khatib-Rahbar, M.

    1988-01-01

    This paper presents an analysis of fission product revaporization from the Reactor Coolant System (RCS) following the Reactor Pressure Vessel (RPV) failure. The station blackout accident in a BWR Mark I Power Plant was considered. The TRAPMELT3 models for vaporization, chemisorption, and the decay heating of RCS structures and gases were used and extended beyond the RPV failure in the analysis. The RCS flow models based on the density-difference or pressure-difference between the RCS and containment pedestal region were developed to estimate the RCS outflow which carries the revaporized fission product to the containment. A computer code called REVAP was developed for the analysis. The REVAP code was incorporated with the MARCH, TRAPMELT3 and NAUA codes from the Source Term Code Package (STCP) to estimate the impact of revaporization on environmental release. The results show that the thermal-hydraulic conditions between the RCS and the pedestal region are important factors in determining the magnitude of revaporization and subsequent release of the volatile fission product into the environment. 6 refs., 8 figs.

  11. Fission Product Transport in TRISO Particle Layers under Operating and Off-Normal Conditions

    SciTech Connect

    Van der Ven, Anton; Was, Gary; Wang, Lumin; Taheri, Mitra

    2014-04-26

    The objective of this project is to determine the diffusivity and chemical behavior of key fission products (ag, Cs, I. Te, Eu and Sr) through SiC and PyC both thermally, under irradiation, and under stress using FP introduction techniques that avoid the pitfalls of past experiments. The experimental approach is to create thin PyC-SiC couples containing the fission product to be studied embedded in the PyC layer. These samples will then be subjected to high temperature exposures in a vacuum and also to irradiation at high temperature, and last, to irradiation under stress at high temperature. The PyC serves as a host layer, providing a means of placing the fission product close to the SiC without damaging the SiC layer by its introduction or losing the FP during heating. Experimental measurements of grain boundary structure and distribution (EBSD, HRTEM, APT) will be used in the modeling effort to determine the qualitative dependence of FP diffusion coefficients on grain boundary orientation, temperature and stress.

  12. Influence of SiC grain boundary character on fission product transport in irradiated TRISO fuel

    SciTech Connect

    Lillo, T. M.; Rooyen, I. J.

    2016-02-26

    The relationship between grain boundary character and fission product migration is identified as an important knowledge gap in order to advance the understanding of fission product release from TRISO fuel particles. Precession electron diffraction (PED), a TEM-based technique, was used in this study to quickly and efficiently provide the crystallographic information needed to identify grain boundary misorientation, grain boundary type (low or high angle) and whether the boundary is coincident site lattice (CSL) – related, in irradiated SiC. Analysis of PED data showed the grain structure of the SiC layer in an irradiated TRISO fuel particle from the AGR-1 experiment to be composed mainly of twin boundaries with a small fraction of low angle grain boundaries (<10%). In general, fission products favor precipitation on random, high angle grain boundaries but can precipitate out on low angle and CSL-related grain boundaries to a limited degree. Pd is capable of precipitating out on all types of grain boundaries but most prominently on random, high angle grain boundaries. Pd-U and Pd-Ag precipitates were found on CSL-related as well as random high angle grain boundaries but not on low angle grain boundaries. In contrast, precipitates containing only Ag were found only on random, high angle grain boundaries but not on either low angle or CSL-related grain boundaries.

  13. Influence of SiC grain boundary character on fission product transport in irradiated TRISO fuel

    DOE PAGES

    Lillo, T. M.; Rooyen, I. J.

    2016-02-26

    The relationship between grain boundary character and fission product migration is identified as an important knowledge gap in order to advance the understanding of fission product release from TRISO fuel particles. Precession electron diffraction (PED), a TEM-based technique, was used in this study to quickly and efficiently provide the crystallographic information needed to identify grain boundary misorientation, grain boundary type (low or high angle) and whether the boundary is coincident site lattice (CSL) – related, in irradiated SiC. Analysis of PED data showed the grain structure of the SiC layer in an irradiated TRISO fuel particle from the AGR-1 experimentmore » to be composed mainly of twin boundaries with a small fraction of low angle grain boundaries (<10%). In general, fission products favor precipitation on random, high angle grain boundaries but can precipitate out on low angle and CSL-related grain boundaries to a limited degree. Pd is capable of precipitating out on all types of grain boundaries but most prominently on random, high angle grain boundaries. Pd-U and Pd-Ag precipitates were found on CSL-related as well as random high angle grain boundaries but not on low angle grain boundaries. In contrast, precipitates containing only Ag were found only on random, high angle grain boundaries but not on either low angle or CSL-related grain boundaries.« less

  14. Photo-fission Product Yield Measurements at Eγ=13 MeV on 235U, 238U, and 239Pu

    NASA Astrophysics Data System (ADS)

    Tornow, W.; Bhike, M.; Finch, S. W.; Krishichayan, Fnu; Tonchev, A. P.

    2016-09-01

    We have measured Fission Product Yields (FPYs) in photo-fission of 235U, 238U, and 239Pu at TUNL's High-Intensity Gamma-ray Source (HI γS) using mono-energetic photons of Eγ = 13 MeV. Details of the experimental setup and analysis procedures will be discussed. Yields for approximately 20 fission products were determined. They are compared to neutron-induced FPYs of the same actinides at the equivalent excitation energies of the compound nuclear systems. In the future photo-fission data will be taken at Eγ = 8 . 0 and 10.5 MeV to find out whether photo-fission exhibits the same so far unexplained dependence of certain FPYs on the energy of the incident probe, as recently observed in neutron-induced fission, for example, for the important fission product 147Nd. Work supported by the U. S. Dept. of Energy, under Grant No. DE-FG02-97ER41033, and by the NNSA, Stewardship Science Academic Alliances Program, Grant No. DE-NA0001838 and the Lawrence Livermore, National Security, LLC under Contract No. DE-AC52-07NA27344.

  15. ICP-MS analysis of fission product diffusion in graphite for High-Temperature Gas-Cooled Reactors

    NASA Astrophysics Data System (ADS)

    Carter, Lukas M.

    Release of radioactive fission products from nuclear fuel during normal reactor operation or in accident scenarios is a fundamental safety concern. Of paramount importance are the understanding and elucidation of mechanisms of chemical interaction, nuclear interaction, and transport phenomena involving fission products. Worldwide efforts to reduce fossil fuel dependence coupled with an increasing overall energy demand have generated renewed enthusiasm toward nuclear power technologies, and as such, these mechanisms continue to be the subjects of vigorous research. High-Temperature Gas-Cooled Reactors (HTGRs or VHTRs) remain one of the most promising candidates for the next generation of nuclear power reactors. An extant knowledge gap specific to HTGR technology derives from an incomplete understanding of fission product transport in major core materials under HTGR operational conditions. Our specific interest in the current work is diffusion in reactor graphite. Development of methods for analysis of diffusion of multiple fission products is key to providing accurate models for fission product release from HTGR core components and the reactor as a whole. In the present work, a specialized diffusion cell has been developed and constructed to facilitate real-time diffusion measurements via ICP-MS. The cell utilizes a helium gas-jet system which transports diffusing fission products to the mass spectrometer using carbon nanoparticles. The setup was designed to replicate conditions present in a functioning HTGR, and can be configured for real-time release or permeation measurements of single or multiple fission products from graphite or other core materials. In the present work, we have analyzed release rates of cesium in graphite grades IG-110, NBG-18, and a commercial grade of graphite, as well as release of iodine in IG-110. Additionally we have investigated infusion of graphite samples with Cs, I, Sr, Ag, and other surrogate fission products for use in release or

  16. Fission Product Monitoring and Release Data for the Advanced Gas Reactor -1 Experiment

    SciTech Connect

    Dawn M. Scates; John B. Walter; Jason M. Harp; Mark W. Drigert; Edward L. Reber

    2010-10-01

    The AGR-1 experiment is a fueled multiple-capsule irradiation experiment that was irradiated in the Advanced Test Reactor (ATR) from December 26, 2006 until November 6, 2009 in support of the Very High Temperature Reactor (VHTR) Technology Development Office (TDO) Fuel Development and Qualification program. An important measure of the fuel performance is the quantification of the fission product releases over the duration of the experiment. To provide this data for the inert fission gasses(Kr and Xe), a fission product monitoring system (FPMS) was developed and implemented to monitor the individual capsule effluents for the radioactive species. The FPMS continuously measured the concentrations of various krypton and xenon isotopes in the sweep gas from each AGR-1 capsule to provide an indicator of fuel irradiation performance. Spectrometer systems quantified the concentrations of Kr-85m, Kr-87, Kr-88, Kr-89, Kr-90, Xe-131m, Xe-133, Xe 135, Xe 135m, Xe-137, Xe-138, and Xe-139 accumulated over repeated eight hour counting intervals.-. To determine initial fuel quality and fuel performance, release activity for each isotope of interest was derived from FPMS measurements and paired with a calculation of the corresponding isotopic production or birthrate. The release activities and birthrates were combined to determine Release-to-Birth ratios for the selected nuclides. R/B values provide indicators of initial fuel quality and fuel performance during irradiation. This paper presents a brief summary of the FPMS, the release to birth ratio data for the AGR-1 experiment and preliminary comparisons of AGR-1 experimental fuels data to fission gas release models.

  17. Fission product release and survivability of UN-kernel LWR TRISO fuel

    SciTech Connect

    T. M. Besmann; M. K. Ferber; H.-T. Lin; B. P. Collin

    2014-05-01

    A thermomechanical assessment of the LWR application of TRISO fuel with UN kernels was performed. Fission product release under operational and transient temperature conditions was determined by extrapolation from fission product recoil calculations and limited data from irradiated UN pellets. Both fission recoil and diffusive release were considered and internal particle pressures computed for both 650 and 800 um diameter kernels as a function of buffer layer thickness. These pressures were used in conjunction with a finite element program to compute the radial and tangential stresses generated within a TRISO particle undergoing burnup. Creep and swelling of the inner and outer pyrolytic carbon layers were included in the analyses. A measure of reliability of the TRISO particle was obtained by computing the probability of survival of the SiC barrier layer and the maximum tensile stress generated in the pyrolytic carbon layers from internal pressure and thermomechanics of the layers. These reliability estimates were obtained as functions of the kernel diameter, buffer layer thickness, and pyrolytic carbon layer thickness. The value of the probability of survival at the end of irradiation was inversely proportional to the maximum pressure.

  18. Experimental determination of the antineutrino spectrum of the fission products of U238.

    PubMed

    Haag, N; Gütlein, A; Hofmann, M; Oberauer, L; Potzel, W; Schreckenbach, K; Wagner, F M

    2014-03-28

    An experiment was performed at the scientific neutron source FRM II in Garching to determine the cumulative antineutrino spectrum of the fission products of U238. Target foils of natural uranium were irradiated with a thermal and a fast neutron beam and the emitted β spectra were recorded with a γ-suppressing electron telescope. The obtained β spectrum of the fission products of U235 was normalized to the data of the magnetic spectrometer BILL. This method strongly reduces systematic errors in the U238 measurement. The β spectrum of U238 was converted into the corresponding ν¯e spectrum. The final ν¯e spectrum is given in 250 keV bins in the range from 2.875 to 7.625 MeV with an energy-dependent error of 3.5% at 3 MeV, 7.6% at 6 MeV, and ≳14% at energies ≳7  MeV (68% confidence level). Furthermore, an energy-independent uncertainty of ∼3.3% due to the absolute normalization is added. Compared to the generally used summation calculations, the obtained spectrum reveals a spectral distortion of ∼10% but returns the same value for the mean cross section per fission for the inverse beta decay.

  19. Selective Trapping of Volatile Fission Products with an Off-Gas Treatment System

    SciTech Connect

    B.R. Westphal; J.J. Park; J.M. Shin; G.I. Park; K.J. Bateman; D.L. Wahlquist

    2008-07-01

    A head-end processing step, termed DEOX for its emphasis on decladding via oxidation, is being developed for the treatment of spent oxide fuel by pyroprocessing techniques. The head-end step employs high temperatures to oxidize UO2 to U3O8 resulting in the separation of fuel from cladding and the removal of volatile fission products. Development of the head-end step is being performed in collaboration with the Korean Atomic Energy Research Institute (KAERI) through an International Nuclear Energy Research Initiative. Following the initial experimentation for the removal of volatile fission products, an off-gas treatment system was designed in conjunction with KAERI to collect specific fission gases. The primary volatile species targeted for trapping were iodine, technetium, and cesium. Each species is intended to be collected in distinct zones of the off-gas system and within those zones, on individual filters. Separation of the volatile off-gases is achieved thermally as well as chemically given the composition of the filter media. A description of the filter media and a basis for its selection will be given along with the collection mechanisms and design considerations. In addition, results from testing with the off-gas treatment system will be presented.

  20. Measurement of tritium production rate distribution for a fusion-fission hybrid conceptual reactor

    NASA Astrophysics Data System (ADS)

    Wang, Xin-Hua; Guo, Hai-Ping; Mou, Yun-Feng; Zheng, Pu; Liu, Rong; Yang, Xiao-Fei; Yang, Jian

    2013-05-01

    A fusion-fission hybrid conceptual reactor is established. It consists of a DT neutron source and a spherical shell of depleted uranium and hydrogen lithium. The tritium production rate (TPR) distribution in the conceptual reactor was measured by DT neutrons using two sets of lithium glass detectors with different thicknesses in the hole in the vertical direction with respect to the D+ beam of the Cockcroft-Walton neutron generator in direct current mode. The measured TPR distribution is compared with the calculated results obtained by the three-dimensional Monte Carlo code MCNP5 and the ENDF/B-VI data file. The discrepancy between the measured and calculated values can be attributed to the neutron data library of the hydrogen lithium lack S(α, β) thermal scattering model, so we show that a special database of low-energy and thermal neutrons should be established in the physics design of fusion-fission hybrid reactors.

  1. Effects of microstructural constraints on the transport of fission products in uranium dioxide at low burnups

    NASA Astrophysics Data System (ADS)

    Lim, Harn Chyi; Rudman, Karin; Krishnan, Kapil; McDonald, Robert; Dickerson, Patricia; Gong, Bowen; Peralta, Pedro

    2016-08-01

    Diffusion of fission gases in UO2 is studied at low burnups, before bubble growth and coalescence along grain boundaries (GBs) become dominant, using a 3-D finite element model that incorporates actual UO2 microstructures. Grain boundary diffusivities are assigned based on crystallography with lattice and GB diffusion coupled with temperature to account for temperature gradients. Heterogeneity of GB properties and connectivity can induce regions where concentration is locally higher than without GB diffusion. These regions are produced by "bottlenecks" in the GB network because of lack of connectivity among high diffusivity GBs due to crystallographic constraints, and they can lead to localized swelling. Effective diffusivities were calculated assuming a uniform distribution of high diffusivity among GBs. Results indicate an increase over the bulk diffusivity with a clear grain size effect and that connectivity and properties of different GBs become important factors on the variability of fission product concentration at the microscale.

  2. Fundamental Studies of Irradiation-Induced Defect Formation and Fission Product Dynamics in Oxide Fuels

    SciTech Connect

    Stubbins, James

    2012-12-19

    The objective of this research program is to address major nuclear fuels performance issues for the design and use of oxide-type fuels in the current and advanced nuclear reactor applications. Fuel performance is a major issue for extending fuel burn-up which has the added advantage of reducing the used fuel waste stream. It will also be a significant issue with respect to developing advanced fuel cycle processes where it may be possible to incorporate minor actinides in various fuel forms so that they can be 'burned' rather than join the used fuel waste stream. The potential to fission or transmute minor actinides and certain long-lived fission product isotopes would transform the high level waste storage strategy by removing the need to consider fuel storage on the millennium time scale.

  3. Detecting special nuclear materials in suspect containers using high-energy gamma rays emitted by fission products

    DOEpatents

    Norman, Eric B.; Prussin, Stanley G.

    2009-01-27

    A method and a system for detecting the presence of special nuclear materials in a suspect container. The system and its method include irradiating the suspect container with a beam of neutrons, so as to induce a thermal fission in a portion of the special nuclear materials, detecting the gamma rays that are emitted from the fission products formed by the thermal fission, to produce a detector signal, comparing the detector signal with a threshold value to form a comparison, and detecting the presence of the special nuclear materials using the comparison.

  4. Detecting special nuclear materials in suspect containers using high-energy gamma rays emitted by fission products

    DOEpatents

    Norman, Eric B.; Prussin, Stanley G.

    2009-01-06

    A method and a system for detecting the presence of special nuclear materials in a suspect container. The system and its method include irradiating the suspect container with a beam of neutrons, so as to induce a thermal fission in a portion of the special nuclear materials, detecting the gamma rays that are emitted from the fission products formed by the thermal fission, to produce a detector signal, comparing the detector signal with a threshold value to form a comparison, and detecting the presence of the special nuclear materials using the comparison.

  5. Detecting special nuclear materials in suspect containers using high-energy gamma rays emitted by fission products

    DOEpatents

    Norman, Eric B [Oakland, CA; Prussin, Stanley G [Kensington, CA

    2009-05-05

    A method and a system for detecting the presence of special nuclear materials in a suspect container. The system and its method include irradiating the suspect container with a beam of neutrons, so as to induce a thermal fission in a portion of the special nuclear materials, detecting the gamma rays that are emitted from the fission products formed by the thermal fission, to produce a detector signal, comparing the detector signal with a threshold value to form a comparison, and detecting the presence of the special nuclear materials using the comparison.

  6. Isomer production ratios and the angular momentum distribution of fission fragments

    NASA Astrophysics Data System (ADS)

    Stetcu, I.; Talou, P.; Kawano, T.; Jandel, M.

    2013-10-01

    Latest generation fission experiments provide an excellent testing ground for theoretical models. In this contribution we compare the measurements for 235U(nth,f), obtained with the Detector for Advanced Neutron Capture Experiments (DANCE) calorimeter at Los Alamos Neutron Science Center (LANSCE), with our full-scale simulation of the primary fragment de-excitation, using the recently developed cgmf code, based on a Monte Carlo implementation of the Hauser-Feshbach theoretical model. We compute the isomer ratios as a function of the initial angular momentum of the fission fragments, for which no direct information exists. Comparison with the available experimental data allows us to determine the initial spin distribution. We also study the dependence of the isomer ratio on the knowledge of the low-lying discrete spectrum input for nuclear fission reactions, finding a high degree of sensitivity. Finally, in the same Hauser-Feshbach approach, we calculate the isomer production ratio for thermal neutron capture on stable isotopes, where the initial conditions (spin, excitation energy, etc.) are well understood. We find that with the current parameters involved in Hauser-Feshbach calculations, we obtain up to a factor of 2 deviation from the measured isomer ratios.

  7. Correlation between Asian Dust and Specific Radioactivities of Fission Products Included in Airborne Samples in Tokushima, Shikoku Island, Japan, Due to the Fukushima Nuclear Accident

    SciTech Connect

    Sakama, M.; Nagano, Y.; Kitade, T.; Shikino, O.; Nakayama, S.

    2014-06-15

    Radioactive fission product {sup 131}I released from the Fukushima Daiichi Nuclear Power Plants (FD-NPP) was first detected on March 23, 2011 in an airborne aerosol sample collected at Tokushima, Shikoku Island, located in western Japan. Two other radioactive fission products, {sup 134}Cs and {sup 137}Cs were also observed in a sample collected from April 2 to 4, 2011. The maximum specific radioactivities observed in this work were about 2.5 to 3.5 mBq×m{sup -3} in a airborne aerosol sample collected on April 6. During the course of the continuous monitoring, we also made our first observation of seasonal Asian Dust and those fission products associated with the FDNPP accident concurrently from May 2 to 5, 2011. We found that the specific radioactivities of {sup 134}Cs and {sup 137}Cs decreased drastically only during the period of Asian Dust. And also, it was found that this trend was very similar to the atmospheric elemental concentration (ng×m{sup -3}) variation of stable cesium ({sup 133}Cs) quantified by elemental analyses using our developed ICP-DRC-MS instrument.

  8. Investigation of the Feasibility of Utilizing Gamma Emission Computed Tomography in Evaluating Fission Product Migration in Irradiated TRISO Fuel Experiments

    SciTech Connect

    Jason M. Harp; Paul A. Demkowicz

    2014-10-01

    In the High Temperature Gas-Cooled Reactor (HTGR) the TRISO particle fuel serves as the primary fission product containment. However the large number of TRISO particles present in proposed HTGRs dictates that there will be a small fraction (~10-4 to 10-5) of as manufactured and in-pile particle failures that will lead to some fission product release. The matrix material surrounding the TRISO particles in fuel compacts and the structural graphite holding the TRISO particles in place can also serve as sinks for containing any released fission products. However data on the migration of solid fission products through these materials is lacking. One of the primary goals of the AGR-3/4 experiment is to study fission product migration from failed TRISO particles in prototypic HTGR components such as structural graphite and compact matrix material. In this work, the potential for a Gamma Emission Computed Tomography (GECT) technique to non-destructively examine the fission product distribution in AGR-3/4 components and other irradiation experiments is explored. Specifically, the feasibility of using the Idaho National Laboratory (INL) Hot Fuels Examination Facility (HFEF) Precision Gamma Scanner (PGS) system for this GECT application is considered. To test the feasibility, the response of the PGS system to idealized fission product distributions has been simulated using Monte Carlo radiation transport simulations. Previous work that applied similar techniques during the AGR-1 experiment will also be discussed as well as planned uses for the GECT technique during the post irradiation examination of the AGR-2 experiment. The GECT technique has also been applied to other irradiated nuclear fuel systems that were currently available in the HFEF hot cell including oxide fuel pins, metallic fuel pins, and monolithic plate fuel.

  9. Deposition of fission and activation products after the Fukushima Dai-ichi nuclear power plant accident.

    PubMed

    Shozugawa, Katsumi; Nogawa, Norio; Matsuo, Motoyuki

    2012-04-01

    The Great Eastern Japan Earthquake on March 11, 2011, damaged reactor cooling systems at Fukushima Dai-ichi nuclear power plant. The subsequent venting operation and hydrogen explosion resulted in a large radioactive nuclide emission from reactor containers into the environment. Here, we collected environmental samples such as soil, plant species, and water on April 10, 2011, in front of the power plant main gate as well as 35 km away in Iitate village, and observed gamma-rays with a Ge(Li) semiconductor detector. We observed activation products ((239)Np and (59)Fe) and fission products ((131)I, (134)Cs ((133)Cs), (137)Cs, (110m)Ag ((109)Ag), (132)Te, (132)I, (140)Ba, (140)La, (91)Sr, (91)Y, (95)Zr, and (95)Nb). (239)Np is the parent nuclide of (239)Pu; (59)Fe are presumably activation products of (58)Fe obtained by corrosion of cooling pipes. The results show that these activation and fission products, diffused within a month of the accident.

  10. A proton-driven, intense, subcritical, fission neutron source for radioisotope production

    SciTech Connect

    Jongen, Y.

    1995-10-01

    {sup 99m}Tc, the most frequently used radioisotope in nuclear medicine, is distributed as {sup 99}Mo=>{sup 99m}Tc generators. {sup 99}Mo is a fission product of {sup 235}U. To replace the aging nuclear reactors used today for this production, the author proposes to use a spallation neutron source, with neutron multiplication by fission. A 150 MeV, H{sup {minus}} cyclotron can produce a 225 kW proton beam with 50% total system energy efficiency. The proton beam would hit a molten lead target, surrounded by a water moderator and a graphite reflector, producing around 0.96 primary neutron per proton. The primary spallation neutrons, moderated, would strike secondary targets containing a subcritical amount of {sup 235}U. The assembly would show a k{sub eff} of 0.8, yielding a fivefold neutron multiplication. The thermal neutron flux at the targets location would be 2 {times} 10{sup 14} n/cm{sup 2}.s, resulting in a fission power of 500 to 750 kW. One such system could supply the world demand in {sup 99}Mo, as well as other radioisotopes. Preliminary indications show that the cost would be lower than the cost of a commercial 10 MW isotope production reactor. The cost of operation, of disposal of radiowaste and of decommissioning should be significantly lower as well. Finally, the non-critical nature of the system would make it more acceptable for the public than a nuclear reactor and should simplify the licensing process.

  11. Implementation of a Thermodynamic Solver within a Computer Program for Calculating Fission-Product Release Fractions

    NASA Astrophysics Data System (ADS)

    Barber, Duncan Henry

    During some postulated accidents at nuclear power stations, fuel cooling may be impaired. In such cases, the fuel heats up and the subsequent increased fission-gas release from the fuel to the gap may result in fuel sheath failure. After fuel sheath failure, the barrier between the coolant and the fuel pellets is lost or impaired, gases and vapours from the fuel-to-sheath gap and other open voids in the fuel pellets can be vented. Gases and steam from the coolant can enter the broken fuel sheath and interact with the fuel pellet surfaces and the fission-product inclusion on the fuel surface (including material at the surface of the fuel matrix). The chemistry of this interaction is an important mechanism to model in order to assess fission-product releases from fuel. Starting in 1995, the computer program SOURCE 2.0 was developed by the Canadian nuclear industry to model fission-product release from fuel during such accidents. SOURCE 2.0 has employed an early thermochemical model of irradiated uranium dioxide fuel developed at the Royal Military College of Canada. To overcome the limitations of computers of that time, the implementation of the RMC model employed lookup tables to pre-calculated equilibrium conditions. In the intervening years, the RMC model has been improved, the power of computers has increased significantly, and thermodynamic subroutine libraries have become available. This thesis is the result of extensive work based on these three factors. A prototype computer program (referred to as SC11) has been developed that uses a thermodynamic subroutine library to calculate thermodynamic equilibria using Gibbs energy minimization. The Gibbs energy minimization requires the system temperature (T) and pressure (P), and the inventory of chemical elements (n) in the system. In order to calculate the inventory of chemical elements in the fuel, the list of nuclides and nuclear isomers modelled in SC11 had to be expanded from the list used by SOURCE 2.0. A

  12. Determination of actinide and fission-product isotopes in very-high-burnup spent nuclear fuel.

    SciTech Connect

    Sullivan, V. S.; Bowers, D. L.; Clark, M. A.; Graczyk, D. G.; Tsai, Y.; Streets, W. E.; Vander Pol, M. H.; Billone, M. C.

    2008-07-01

    A work plan was desired that would produce data for a wide array of actinide and fission-product isotopes with reasonably good accuracy and relatively low cost. An analysis scheme involving a fairly small number of separations, dilutions, and measurement methods was used to generate information on 74 isotopes in two spent-fuel samples of >70 GWd/MTU burnup. Some of the measured isotopes are of high interest for burnup-credit evaluations and had not been reported previously for high-burnup fuels.

  13. New accurate measurements of neutron emission probabilities for relevant fission products

    NASA Astrophysics Data System (ADS)

    Agramunt, J.; Tain, J. L.; Albiol, F.; Algora, A.; Caballero-Folch, R.; Calviño, F.; Cortes, G.; Dillmann, I.; Eronen, T.; Garcia, A. R.; Ganioglu, E.; Gelletly, W.; Gorelov, D.; Guadilla, V.; Hakala, H.; Jokinen, A.; Kankainen, A.; Montaner, A.; Marta, M.; Mendoza, E.; Moore, I.; Nobs, C.; Orrigo, S.; Penttila, H.; Reponen, M.; Rinta-Antila, S.; Riego, A.; Rubio, B.; Saastamoinen, A.; Salvador-Castiñeira, P.; Tarifeño-Saldivia, A.; Tolosa, A.; Valencia, E.

    2017-09-01

    We have performed new accurate measurements of the beta-delayed neutron emission probability for ten isotopes of the elements Y, Sb, Te and I. These are fission products that either have a significant contribution to the fraction of delayed neutrons in reactors or are relatively close to the path of the astrophysical r process. The measurements were performed with isotopically pure radioactive beams using a constant and high efficiency neutron counter and a low noise beta detector. Preliminary results are presented for six of the isotopes and compared with previous measurements and theoretical calculations.

  14. Design and Expected Performance of the AGR-1 Fission Product Monitoring System (FPMS)

    SciTech Connect

    John K. Hartwell; Dawn M. Scates

    2005-09-01

    The effluent from each test capsule of the AGR-1 experiment will be monitored by a detector system consisting of a gamma-ray spectrometer and a gross radiation detector. This collection of radiation measurement systems will be known as the AGR-1 Fission Product Monitoring System (FPMS). Proper design and functioning of the FPMS is critical to the success of the AGR-1 fuel test experiment.This document describes the AGR-1 FPMS and presents calculations indicating that this design will meet the pertinent test requirements.

  15. Fission-product data analysis from actinide samples exposed in the Dounreay Prototype Fast Reactor

    SciTech Connect

    Murphy, B.D.; Dickens, J.K.; Walker, R.L.; Newton, T.D.

    1994-12-31

    Since 1979 a cooperative agreement has been in effect between the United States and the United Kingdom to investigate the irradiation of various actinide species placed in the core of the Dounreay Prototype Fast Reactor (PFR). The irradiated species were isotopes of thorium, protactinium, uranium, neptunium, plutonium, americium, and curium. A set of actinide samples (mg quantities) was exposed to about 490 effective full power days (EFPD) of reactor operations. The fission-product results are reported here. The actinide results will be report elsewhere.

  16. Ion exchange in the atomic energy industry with particular reference to actinide and fission product separation

    SciTech Connect

    Jenkins, I.L.

    1984-01-01

    Reviewed are some of the uses of ion exchange processes used by the nuclear industry for the period April, 1978 to April, 1983. The topics dealt with are: thorium, protactinium, uranium, neptunium, plutonium, americium, cesium and actinide-lanthanide separations; the higher actinides - Cm, Bk, Cf, Es and Fm; fission products; ion exchange in the geological disposal of radioactive waste. Consideration is given to safety in the use of ion exchangers and in safe methods of disposal of such materials. Full scale and pilot plant process descriptions are included as well as summaries of laboratory studies. 130 references.

  17. MICRO/NANO-STRUCTURAL EXAMINATION AND FISSION PRODUCT IDENTIFICATION IN NEUTRON IRRADIATED AGR-1 TRISO FUEL

    SciTech Connect

    van Rooyen, I. J.; Lillo, T. M.; Wen, H. M.; Hill, C. M.; Holesinger, T. G.; Wu, Y. Q.; Aguiara, J. A.

    2016-11-01

    Advanced microscopic and microanalysis techniques were developed and applied to study irradiation effects and fission product behavior in selected low-enriched uranium oxide/uranium carbide TRISO-coated particles from fuel compacts in six capsules irradiated to burnups of 11.2 to 19.6% FIMA. Although no TRISO coating failures were detected during the irradiation, the fraction of Ag-110m retained in individual particles often varied considerably within a single compact and at the capsule level. At the capsule level Ag-110m release fractions ranged from 1.2 to 38% and within a single compact, silver release from individual particles often spanned a range that extended from 100% retention to nearly 100% release. In this paper, selected irradiated particles from Baseline, Variant 1 and Variant 3 type fueled TRISO coated particles were examined using Scanning Electron Microscopy, Atom Probe Tomography; Electron Energy Loss Spectroscopy; Precession Electron Diffraction, Transmission Electron Microscopy, Scanning Transmission Electron Microscopy (STEM), High Resolution Electron Microscopy (HRTEM) examinations and Electron Probe Micro-Analyzer. Particle selection in this study allowed for comparison of the fission product distribution with Ag retention, fuel type and irradiation level. Nano sized Ag-containing features were predominantly identified in SiC grain boundaries and/or triple points in contrast with only two sitings of Ag inside a SiC grain in two different compacts (Baseline and Variant 3 fueled compacts). STEM and HRTEM analysis showed evidence of Ag and Pd co-existence in some cases and it was found that fission product precipitates can consist of multiple or single phases. STEM analysis also showed differences in precipitate compositions between Baseline and Variant 3 fuels. A higher density of fission product precipitate clusters were identified in the SiC layer in particles from the Variant 3 compact compared with the Variant 1 compact. Trend analysis shows

  18. Transport of fission products with a helium gas-jet at TRIGA-SPEC

    NASA Astrophysics Data System (ADS)

    Eibach, M.; Beyer, T.; Blaum, K.; Block, M.; Eberhardt, K.; Herfurth, F.; Geppert, C.; Ketelaer, J.; Ketter, J.; Krämer, J.; Krieger, A.; Knuth, K.; Nagy, Sz.; Nörtershäuser, W.; Smorra, C.

    2010-02-01

    A helium gas-jet system for the transport of fission products from the research reactor TRIGA Mainz has been developed, characterized and tested within the TRIGA-SPEC experiment. For the first time at TRIGA Mainz carbon aerosol particles have been used for the transport of radionuclides from a target chamber with high efficiency. The radionuclides have been identified by means of γ-spectroscopy. Transport time, efficiency as well as the absolute number of transported radionuclides for several species have been determined. The design and the characterization of the gas-jet system are described and discussed.

  19. Fission product release phenomena during core melt accidents in metal fueled heavy water reactors

    SciTech Connect

    Ellison, P G; Hyder, M L; Monson, P R; Randolph, H W; Hagrman, D L; McClure, P R; Leonard, M T

    1990-01-01

    The phenomena that determine fission product release rates from a core melting accident in a metal-fueled, heavy water reactor are described in this paper. This information is obtained from the analysis of the current metal fuel experimental data base and from the results of analytical calculations. Experimental programs in place at the Savannah River Site are described that will provide information to resolve uncertainties in the data base. The results of the experiments will be incorporated into new severe accident computer codes recently developed for this reactor design. 47 refs., 4 figs.

  20. Behavior of metallic fission products in uranium plutonium mixed oxide fuel

    NASA Astrophysics Data System (ADS)

    Sato, I.; Furuya, H.; Arima, T.; Idemitsu, K.; Yamamoto, K.

    1999-08-01

    Metallic fission products, ruthenium, rhodium, technetium, palladium, and molybdenum, exist in irradiated oxide fuels as metallic inclusions. In this work, the radial distributions of metallic inclusion constituents in the fuel specimen irradiated to a peak burnup of 7-13 at.% were observed with an electron probe microanalysis. Palladium concentration is high at the periphery in all the specimens. Molybdenum shows the same tendency for the 13 at.% burnup specimen. These results showed the significant difference between experimental data and calculations with ORIGEN-2 at such high burnups, which suggested that the migration of palladium and molybdenum was controlled mainly by diffusion of gaseous species containing each metal along the fuel temperature gradient.

  1. Monte Carlo Models for the Production of beta-delayed Gamma Rays Following Fission of Special Nuclear Materials

    SciTech Connect

    Pruet, J; Prussin, S; Descalle, M; Hall, J

    2004-02-03

    A Monte Carlo method for the estimation of {beta}-delayed {gamma}-ray spectra following fission is described that can accommodate an arbitrary time-dependent fission rate and photon collection history. The method invokes direct sampling of the independent fission yield distributions of the fissioning system, the branching ratios for decay of individual fission products and the spectral distributions for photon emission for each decay mode. Though computationally intensive, the method can provide a detailed estimate of the spectrum that would be recorded by an arbitrary spectrometer, and can prove useful in assessing the quality of evaluated data libraries, for identifying gaps in these libraries, etc. The method is illustrated by a first comparison of calculated and experimental spectra from decay of short-lived fission products following the reactions {sup 235}U(n{sub th}, f) and {sup 239}Pu(n{sub th}, f). For general purpose transport calculations, where detailed consideration of the large number of individual {gamma}-ray transitions in a spectrum may be unnecessary, it is shown that an accurate and simple parameterization of a {gamma}-ray source function can be obtained. These parametrizations should provide high-quality average spectral distributions that should prove useful in calculations describing photons escaping from thick attenuating media.

  2. Chemical thermodynamics of Cs and Te fission product interactions in irradiated LMFBR mixed-oxide fuel pins

    NASA Astrophysics Data System (ADS)

    Adamson, M. G.; Aitken, E. A.; Lindemer, T. B.

    1985-02-01

    A combination of fuel chemistry modelling and equilibrium thermodynamic calculations has been used to predict the atom ratios of Cs and Te fission products (Cs:Te) that find their way into the fuel-cladding interface region of irradiated stainless steel-clad mixed-oxide fast breeder reactor fuel pins. It has been concluded that the ratio of condensed, chemically-associated Cs and Te in the interface region,Čs:Te, which in turn determines the Te activity, is controlled by an equilibrium reaction between Cs 2Te and the oxide fuel, and that the value of Čs:Te is, depending on fuel 0:M, either equal to or slightly less than 2:1. Since Cs and Te fission products are both implicated as causative agents in FCCI (fission product-assisted inner surface attack of stainless steel cladding) and in FPLME (fission product-assisted liquid metal embrittlement of AISI-Type 316), the observed out-of-pile Cs:Te thresholds for FCCI (4˜:1) and FPLME (2˜:1) have been rationalized in terms of Cs:Te thermochemistry and phase equilibria. Also described in the paper is an updated chemical evolution model for reactive/volatile fission product behavior in irradiated oxide pins.

  3. Atmospheric products from the Upper Atmosphere Research Satellite (UARS)

    NASA Technical Reports Server (NTRS)

    Ahmad, Suraiya P.; Johnson, James E.; Jackman, Charles H.

    2003-01-01

    This paper provides information on the products available at the NASA Goddard Earth Sciences (GES) Distributed Active Archive Center (DAAC) from the Upper Atmosphere Research Satellite (UARS) mission. The GES DAAC provides measurements from the primary UARS mission, which extended from launch in September 1991 through September 2001. The ten instruments aboard UARS provide measurements of atmospheric trace gas species, dynamical variables, solar irradiance input, and particle energy flux. All standard Level 3 UARS products from all ten instruments are offered free to the public and science user community. The Level 3 data are geophysical parameters, which have been transformed into a common format and equally spaced along the measurement trajectory. The UARS data have been reprocessed several times over the years following improvements to the processing algorithms. The UARS data offered from the GES DAAC are the latest versions of each instrument. The UARS data may be accessed through the GES DAAC website at

  4. METHOD FOR SEPARATION OF PLUTONIUM FROM URANIUM AND FISSION PRODUCTS BY SOLVENT EXTRACTION

    DOEpatents

    Seaborg, G.T.; Blaedel, W.J.; Walling, M.T. Jr.

    1960-08-23

    A process is given for separating from each other uranium, plutonium, and fission products in an aqueous nitric acid solution by the so-called Redox process. The plutonium is first oxidized to the hexavalent state, e.g., with a water-soluble dichromate or sodium bismuthate, preferably together with a holding oxidant such as potassium bromate. potassium permanganate, or an excess of the oxidizing agent. The solution is then contacted with a water-immiscible organic solvent, preferably hexone. whereby uranium and plutonium are extracted while the fission products remain in the aqueous solution. The separated organic phase is then contacted with an aqueous solution of a reducing agent, with or without a holding reductant (e.g., with a ferrous salt plus hydrazine or with ferrous sulfamate), whereby plutonium is reduced to the trivalent state and back- extracted into the aqueous solution. The uranium may finally be back-extracted from the organic solvent (e.g., with a 0.1 N nitric acid).

  5. MODELING AND ANALYSIS OF FISSION PRODUCT TRANSPORT IN THE AGR-3/4 EXPERIMENT

    SciTech Connect

    Humrickhouse, Paul W.; Collin, Blaise P.; Hawkes, Grant L.; Harp, Jason M.; Demkowicz, Paul A.; Petti, David A.

    2016-11-01

    In this work we describe the ongoing modeling and analysis efforts in support of the AGR-3/4 experiment. AGR-3/4 is intended to provide data to assess fission product retention and transport (e.g., diffusion coefficients) in fuel matrix and graphite materials. We describe a set of pre-test predictions that incorporate the results of detailed thermal and fission product release models into a coupled 1D radial diffusion model of the experiment, using diffusion coefficients reported in the literature for Ag, Cs, and Sr. We make some comparisons of the predicted Cs profiles to preliminary measured data for Cs and find these to be reasonable, in most cases within an order of magnitude. Our ultimate objective is to refine the diffusion coefficients using AGR-3/4 data, so we identify an analytical method for doing so and demonstrate its efficacy via a series of numerical experiments using the model predictions. Finally, we discuss development of a post-irradiation examination plan informed by the modeling effort and simulate some of the heating tests that are tentatively planned.

  6. Influence of SiC grain boundary character on fission product transport in irradiated TRISO fuel

    NASA Astrophysics Data System (ADS)

    Lillo, T. M.; van Rooyen, I. J.

    2016-05-01

    In this study, the fission product precipitates at silicon carbide grain boundaries from an irradiated TRISO particle were identified and correlated with the associated grain boundary characteristics. Precession electron diffraction in the transmission electron microscope provided the crystallographic information needed to identify grain boundary misorientation and boundary type (i.e., low angle, random high angle or coincident site lattice (CSL)-related). The silicon carbide layer was found to be composed mainly of twin boundaries and small fractions of random high angle and low angle grain boundaries. Most fission products were found at random, high-angle grain boundaries, with small fractions at low-angle and CSL-related grain boundaries. Palladium (Pd) was found at all types of grain boundaries while Pd-uranium and Pd-silver precipitates were only associated with CSL-related and random, high-angle grain boundaries. Precipitates containing only Ag were found only at random, high-angle grain boundaries, but not at low angle or CSL-related grain boundaries.

  7. Fission Product Appearance Rate Coefficients in Design Basis Source Term Determinations - Past and Present

    NASA Astrophysics Data System (ADS)

    Perez, Pedro B.; Hamawi, John N.

    2017-09-01

    Nuclear power plant radiation protection design features are based on radionuclide source terms derived from conservative assumptions that envelope expected operating experience. Two parameters that significantly affect the radionuclide concentrations in the source term are failed fuel fraction and effective fission product appearance rate coefficients. Failed fuel fraction may be a regulatory based assumption such as in the U.S. Appearance rate coefficients are not specified in regulatory requirements, but have been referenced to experimental data that is over 50 years old. No doubt the source terms are conservative as demonstrated by operating experience that has included failed fuel, but it may be too conservative leading to over-designed shielding for normal operations as an example. Design basis source term methodologies for normal operations had not advanced until EPRI published in 2015 an updated ANSI/ANS 18.1 source term basis document. Our paper revisits the fission product appearance rate coefficients as applied in the derivation source terms following the original U.S. NRC NUREG-0017 methodology. New coefficients have been calculated based on recent EPRI results which demonstrate the conservatism in nuclear power plant shielding design.

  8. Diffusion modeling of fission product release during depressurized core conduction cooldown conditions

    SciTech Connect

    Martin, R.C.

    1990-01-01

    A simple model for diffusion through the silicon carbide layer of TRISO particles is applied to the data for accident condition testing of fuel spheres for the High-Temperature Reactor program of the Federal Republic of Germany (FRG). Categorization of sphere release of {sup 137}Cs based on fast neutron fluence permits predictions of release with an accuracy comparable to that of the US/FRG accident condition fuel performance model. Calculations are also performed for {sup 85}Kr, {sup 90}Sr, and {sup 110m}Ag. Diffusion of cesium through SiC suggests that models of fuel failure should consider fuel performance during repeated accident condition thermal cycling. Microstructural considerations in models in fission product release are discussed. The neutron-induced segregation of silicon within the SiC structure is postulated as a mechanism for enhanced fission product release during accident conditions. An oxygen-enhanced SiC decomposition mechanism is also discussed. 12 refs., 11 figs., 2 tabs.

  9. Equilibrium and nonequilibrium partition coefficients of volatile fission products between liquid sodium and the gas phase

    SciTech Connect

    Haga, K.; Nishizawa, Y.; Watanabe, T.; Miyahara, S.; Himeno, Y. )

    1992-02-01

    Two series of experiments have been conducted to obtain the gas-liquid equilibrium partition coefficient K{sub d} and the nonequilibrium partition coefficient K{prime}{sub d} of volatile fission products such as cesium, iodine, and tellurium between liquid sodium and the gas phase. In the equilibrium experiment, a sodium pool mixed with a fission product simulant was heated by a n electric furnace, and the solvent of the vapors and aerosols trapped by filters was quantitatively analyzed. The results provided in this paper are as follows: Cesium shows the largest K{sub d} (20 to 100). The K{sub d} values of cesium and iodine agree well with the theoretical ones reported by Castleman and Tang. If sodium telluride, which is harder to vaporize than pure tellurium, is assumed, the measured K{sub d} value of tellurium agrees with the theoretical. The nonequilibrium experiment in which the temperature dropped relatively sharply in the cover-gas region shows that K{prime}{sub d} was not larger than K{sub d}.

  10. Role of ( n,2 n) reactions in transmutation of long-lived fission products

    NASA Astrophysics Data System (ADS)

    Apse, V. A.; Kulikov, G. G.; Kulikov, E. G.

    2016-12-01

    The conditions under which ( n,γ) and ( n,2 n) reactions can help or hinder each other in neutron transmutation of long-lived fission products (LLFPs) are considered. Isotopic and elemental transmutation for the main long-lived fission products, 79Se, 93Zr, 99Tc, 107Pd, 126Sn, 129I, and 135Cs, are considered. The effect of ( n,2 n) reactions on the equilibrium amount of nuclei of the transmuted isotope and the neutron consumption required for the isotope processing is estimated. The aim of the study is to estimate the influence of ( n,2 n) reactions on efficiency of neutron LLFP transmutation. The code TIME26 and the libraries of evaluated nuclear data ABBN-93, JEF-PC, and JANIS system are applied. The following results are obtained: (1) The effect of ( n,2 n) reactions on the minimum number of neutrons required for transmutation and the equilibrium amount of LLFP nuclei is estimated. (2) It is demonstrated that, for three LLFP isotopes (126Sn, 129I, and 135Cs), ( n,γ) and ( n,2 n) reactions are partners facilitating neutron transmutation. The strongest effect of ( n,2 n) reaction is found for 126Sn transmutation (reduction of the neutron consumption by 49% and the equilibrium amount of nuclei by 19%).

  11. Investigation of Fission Product Transport into Zeolite-A for Pyroprocessing Waste Minimization

    SciTech Connect

    James R. Allensworth; Michael F. Simpson; Man-Sung Yim; Supathorn Phongikaroon

    2013-02-01

    Methods to improve fission product salt sorption into zeolite-A have been investigated in an effort to reduce waste associated with the electrochemical treatment of spent nuclear fuel. It was demonstrated that individual fission product chloride salts were absorbed by zeolite-A in a solid-state process. As a result, recycling of LiCl-KCl appears feasible via adding a zone-freezing technique to the current treatment process. Ternary salt molten-state experiments showed the limiting kinetics of CsCl and SrCl2 sorption into the zeolite. CsCl sorption occurred rapidly relative to SrCl2 with no observed dependence on zeolite particle size, while SrCl2 sorption was highly dependent on particle size. The application of experimental data to a developed reaction-diffusion-based sorption model yielded diffusivities of 8.04 × 10-6 and 4.04 × 10-7 cm2 /s for CsCl and SrCl2, respectively. Additionally, the chemical reaction term in the developed model was found to be insignificant compared to the diffusion term.

  12. High-level waste glass field burial test: leaching and migration of fission products

    SciTech Connect

    Melnyk, T.W.; Johnson, L.H.; Walton, F.B.

    1984-01-01

    In June 1960, 25 nepheline syenite-based glass hemispheres containing the fission products /sup 137/Cs, /sup 90/Sr, /sup 144/Ce and /sup 106/Ru were buried below the water table in a sandy-soil aquifer at the Chalk River Nuclear Laboratories of Atomic Energy of Canada Limited. Measurements of soil and groundwater concentrations of /sup 90/Sr and /sup 137/Cs have been interpreted using non-equilibrium migration models to deduce the leaching history of the glass for these burial conditions. The leaching history derived from the field data has been compared to laboratory leaching of samples taken from a glass hemisphere retrieved in 1978, and also to pre-burial laboratory leaching of identical hemispheres. The time dependence of the leach rates observed for the buried specimens suggests that leaching is inhibited by the formation of a protective surface layer. The effect of the kinetic limitations of the fission-product/sandy-soil interactions is discussed with respect to the migration of /sup 90/Sr and /sup 137/Cs over a 20 year time scale. It is concluded that kinetically limited sorption by oxyhdroxides, rather than equilibrium ion exchange, controls the long-term migration of /sup 90/Sr. Cesium is initially rapidly bound to the micaceous fraction of the sand, but slow remobilization of /sup 137/Cs in particulate form is observed and is believed to be related to bacterial action.

  13. Role of (n,2n) reactions in transmutation of long-lived fission products

    SciTech Connect

    Apse, V. A.; Kulikov, G. G. Kulikov, E. G.

    2016-12-15

    The conditions under which (n,γ) and (n,2n) reactions can help or hinder each other in neutron transmutation of long-lived fission products (LLFPs) are considered. Isotopic and elemental transmutation for the main long-lived fission products, {sup 79}Se, {sup 93}Zr, {sup 99}Tc, {sup 107}Pd, {sup 126}Sn, {sup 129}I, and {sup 135}Cs, are considered. The effect of (n,2n) reactions on the equilibrium amount of nuclei of the transmuted isotope and the neutron consumption required for the isotope processing is estimated. The aim of the study is to estimate the influence of (n,2n) reactions on efficiency of neutron LLFP transmutation. The code TIME26 and the libraries of evaluated nuclear data ABBN-93, JEF-PC, and JANIS system are applied. The following results are obtained: (1) The effect of (n,2n) reactions on the minimum number of neutrons required for transmutation and the equilibrium amount of LLFP nuclei is estimated. (2) It is demonstrated that, for three LLFP isotopes ({sup 126}Sn, {sup 129}I, and {sup 135}Cs), (n,γ) and (n,2n) reactions are partners facilitating neutron transmutation. The strongest effect of (n,2n) reaction is found for {sup 126}Sn transmutation (reduction of the neutron consumption by 49% and the equilibrium amount of nuclei by 19%).

  14. Assessment of thermal gradient tube results from the HI series of fission product release tests

    SciTech Connect

    Norwood, K.S.

    1985-03-01

    A thermal gradient tube was used to analyze fission product vapors released from fuel heated in the HI test series. Complete deposition profiles were obtained for Cs, I, Ag, and Sb. The cesium profiles were complex and probably were dominated by Cs-S-O compounds formed by release of sulfur from furnace ceramics. The iodine profiles were simple, indicating that more than 99.5% of the released iodine behaved as a single nonvolatile species, probably CsI. Mass transfer coefficients for this species onto platinum were estimated to be 1.9 to 5.8 cm/s. Silver was probably released in elemental form, condensed to an aerosol, and captured by filters. Antimony was released as the element and reacted rapidly with platinum (or gold) as it deposited. Antimony profiles were calculated a priori with some success. A method was developed for isolating tellurium from platinum and mixed fission products in a form suitable for neutron activation analysis. The platinum samples were completely dissolved in acid (HCl/HNO/sub 3/), and the tellurium was precipitated on selenium carrier by reduction. Finally, tellurium was loaded onto Dowex 1X-4 ion-exchange resin for activation and analysis. Tellurium recovery was approx. 88%, and the theoretical sensitivity was approx. 30 ng.

  15. The chemical state of fission products in oxide fuels at different stages of the nuclear fuel cycle

    SciTech Connect

    Kleykamp, H.

    1988-03-01

    A survey of work at the Kernforschungszentrum Karlsruhe is presented on the chemical state of selected fission products that are relevant in the fuel cycle of light water reactor (LWR) and fast breeder reactor fuels. The influence of fuel type and irradiation progress on the composition of the Mo-Tc-Ru-Rh-Pd fission product alloys precipitated in the oxide matrix is examined using the respective multicomponent phase diagrams. The kinetics of dissolution of these phases in nitric acid at the reprocessing stage is discussed. Composition and structure of the residues, and the reprecipitation phenomena from highly active waste (HAW), are elucidated. A second metamorphosis of the fission products is recognized during the vitrification process. The formation of Ru(Rh) oxide and Pd(Rh, U, Te) alloys in simulated vitrified HAW concentrate and in HAW concentrate from the reprocessing of irradiated LWR fuels in interpreted on the basis of heterogeneous equilibria.

  16. Fission Product Monitoring of TRISO Coated Fuel For The Advanced Gas Reactor -1 Experiment

    SciTech Connect

    Dawn M. Scates; John K. Hartwell; John b. Walter

    2010-10-01

    The US Department of Energy has embarked on a series of tests of TRISO-coated particle reactor fuel intended for use in the Very High Temperature Reactor (VHTR) as part of the Advanced Gas Reactor (AGR) program. The AGR-1 TRISO fuel experiment, currently underway, is the first in a series of eight fuel tests planned for irradiation in the Advanced Test Reactor (ATR) located at the Idaho National Laboratory (INL). The AGR-1 experiment reached a peak compact averaged burn up of 9% FIMA with no known TRISO fuel particle failures in March 2008. The burnup goal for the majority of the fuel compacts is to have a compact averaged burnup greater than 18% FIMA and a minimum compact averaged burnup of 14% FIMA. At the INL the TRISO fuel in the AGR-1 experiment is closely monitored while it is being irradiated in the ATR. The effluent monitoring system used for the AGR-1 fuel is the Fission Product Monitoring System (FPMS). The FPMS is a valuable tool that provides near real-time data indicative of the AGR-1 test fuel performance and incorporates both high-purity germanium (HPGe) gamma-ray spectrometers and sodium iodide [NaI(Tl)] scintillation detector-based gross radiation monitors. To quantify the fuel performance, release-to-birth ratios (R/B’s) of radioactive fission gases are computed. The gamma-ray spectra acquired by the AGR-1 FPMS are analyzed and used to determine the released activities of specific fission gases, while a dedicated detector provides near-real time count rate information. Isotopic build up and depletion calculations provide the associated isotopic birth rates. This paper highlights the features of the FPMS, encompassing the equipment, methods and measures that enable the calculation of the release-to-birth ratios. Some preliminary results from the AGR-1 experiment are also presented.

  17. Fission Product Monitoring of TRISO Coated Fuel For The Advanced Gas Reactor -1 Experiment

    SciTech Connect

    Dawn M. Scates; John K Hartwell; John B. Walter

    2008-09-01

    The US Department of Energy has embarked on a series of tests of TRISO-coated particle reactor fuel intended for use in the Very High Temperature Reactor (VHTR) as part of the Advanced Gas Reactor (AGR) program. The AGR-1 TRISO fuel experiment, currently underway, is the first in a series of eight fuel tests planned for irradiation in the Advanced Test Reactor (ATR) located at the Idaho National Laboratory (INL). The AGR-1 experiment reached a peak compact averaged burn up of 9% FIMA with no known TRISO fuel particle failures in March 2008. The burnup goal for the majority of the fuel compacts is to have a compact averaged burnup greater than 18% FIMA and a minimum compact averaged burnup of 14% FIMA. At the INL the TRISO fuel in the AGR-1 experiment is closely monitored while it is being irradiated in the ATR. The effluent monitoring system used for the AGR-1 fuel is the Fission Product Monitoring System (FPMS). The FPMS is a valuable tool that provides near real-time data indicative of the AGR-1 test fuel performance and incorporates both high-purity germanium (HPGe) gamma-ray spectrometers and sodium iodide [NaI(Tl)] scintillation detector-based gross radiation monitors. To quantify the fuel performance, release-to-birth ratios (R/B’s) of radioactive fission gases are computed. The gamma-ray spectra acquired by the AGR-1 FPMS are analyzed and used to determine the released activities of specific fission gases, while a dedicated detector provides near-real time count rate information. Isotopic build up and depletion calculations provide the associated isotopic birth rates. This paper highlights the features of the FPMS, encompassing the equipment, methods and measures that enable the calculation of the release-to-birth ratios. Some preliminary results from the AGR-1 experiment are also presented.

  18. Electron microscopic evaluation and fission product identification of irradiated TRISO coated particles from the AGR-1 experiment: A preliminary Study

    SciTech Connect

    I J van Rooyen; D E Janney; B D Miller; J L Riesterer; P A Demkowicz

    2012-10-01

    ABSTRACT Post-irradiation examination of coated particle fuel from the AGR-1 experiment is in progress at Idaho National Laboratory and Oak Ridge National Laboratory. In this presentation a brief summary of results from characterization of microstructures in the coating layers of selected irradiated fuel particles with burnup of 11.3% and 19.3% FIMA will be given. The main objective of the characterization were to study irradiation effects, fuel kernel porosity, layer debonding, layer degradation or corrosion, fission-product precipitation, grain sizes, and transport of fission products from the kernels across the TRISO layers. Characterization techniques such as scanning electron microscopy, transmission electron microscopy, energy dispersive spectroscopy, and wavelength dispersive spectroscopy were used. A new approach to microscopic quantification of fission-product precipitates is also briefly demonstrated. The characterization emphasized fission-product precipitates in the SiC-IPyC interface, SiC layer and the fuel-buffer interlayer, and provided significant new insights into mechanisms of fission-product transport. Although Pd-rich precipitates were identified at the SiC-IPyC interlayer, no significant SiC-layer thinning was observed for the particles investigated. Characterization of these precipitates highlighted the difficulty of measuring low concentration Ag in precipitates with significantly higher concentrations of contain Pd and U. Different approaches to resolving this problem are discussed. Possible microstructural differences between particles with high and low releases of Ag particles are also briefly discussed, and an initial hypothesis is provided to explain fission-product precipitate compositions and locations. No SiC phase transformations or debonding of the SiC-IPyC interlayer as a result of irradiation were observed. Lessons learned from the post-irradiation examination are described and future actions are recommended.

  19. Review of ENDF/B-VI Fission-Product Cross Section

    SciTech Connect

    Wright, R.Q.

    1999-01-01

    the uncertainty in calculated results and provide a better interpretation of criticality safety margins. Thus, the thrust of the Nuclear Data Task is to obtain high-resolution data in the intermediate energy region and provide fits to the data that utilize the modern RM formalism and covariance information for subsequent use in criticality predictability applications. As a subtask of the Nuclear Data Task, this review of the fission-product cross sections has several objectives. The first objective is a general data status review at various levels for the some 200 fission products. The second objective is a more detailed investigation of the top 20 fission products with regard to thermal- and intermediate-energy capture and scatter cross sections. The third objective is to demonstrate the revision of ENDF/B evaluations utilizing new data and evaluation techniques for 13 fission products. The fourth objective is to make recommendations for improvements, both specific and general in nature.

  20. Implementation of a new gamma spectrometer on the MERARG loop: Application to the volatile fission products release measurement

    SciTech Connect

    Bernard, S.; Gleizes, B.; Pontillon, Y.; Hanus, E.; Ducros, G.; Roure, C.

    2015-07-01

    The MERARG facility initially aims at the annealing of irradiated fuel samples to study the gaseous fission products release kinetics. In order to complete the evaluation of the source term potentially released during accidental situation, the MERARG experimental circuit has been enhanced with a new gamma spectrometer. This one is directly sighting the fuel and is devoted to the fission products release kinetics. Because of the specificities of the fuel measurements, it has been dimensioned and designed to match the specific requirements. The acquisition chain and the collimation system have been optimized for this purpose and a first set of two experiments have shown the good functioning of this new spectrometry facility. (authors)

  1. Beta spectroscopy of some neutron-rich cerium isotopes in252Cf fission products

    NASA Astrophysics Data System (ADS)

    Ebong, I. D. U.; Roy, R. R.

    1981-09-01

    The method of cyclic-time optimization has been used, in conjunction with a beta-Kx-ray coincidence technique, to obtain the beta spectrum of some decaying cerium isotopes in the fission products of252Cf. A Kurie plot of the beta spectrum revealed at least four beta groups. From the relative isotopic yields of Kx-ray the isotopic origin of each group has been determined. The coincidence method used in this study allows the measurement of beta groups feeding excited levels of daughter products with high internal conversion coefficients. The end-point energies and isotopic origin of the measured beta groups were as follows: 2.349(±0.100)MeV,145Ce; 1.715(±0.103)MeV,145Ce and148Ce; 1.267 (±0.103)MeV,145Ce; 0.748(±0.109) MeV,146Ce and148Ce.

  2. Actinide, Elemental, and Fission Product Measurements by ICPMS at the Savannah River Site

    SciTech Connect

    Tovo, L.L.; Waller, P.R.; Clymire, J.; Jones, V.D.; Boyce, W.T.

    1998-03-01

    VG Elemental Inductively coupled plasma-mass spectrometer (ICPMS), PlasmaQuad 1 (PQ1) Model No. 4, installed in a radiohood, is used by the Savannah River Technology Center to provide non-routine mass measurements for environmental monitoring, waste tank characterization studies, isotope ratios for criticality determinations, and the measurement of elemental, fission product, and actinide mass distributions of the glass product from the Defense Waste Processing Facility (DWPF). Modifications to improve instrument reliability, sample preparation, and data handling, as well as modifications to the laboratory that permit measurements in a radioactive environment will be discussed. Based on our operating experience, two laboratory facilities are being prepared for additional instruments to operate in a radioactive environment. A separate instrument is being installed for non-radioactive measurements and method development.

  3. A cyclic time optimization approach to the study of 252Cf fission products

    NASA Astrophysics Data System (ADS)

    Price, R. I.; Ebong, I. D. U.; Adams, John A.; Roy, R. R.

    1980-05-01

    A K X-ray-beta particle coincidence technique has been investigated for the study of the beta decay of fission products from 252Cf. A fission-fragments transport system has been developed and its optimization curve used for the identification of the half-life associated with the K X-ray peak originating from the Mo → Tc decay high-resolution lithium-drifted silicon spectrometer and a plastic scintillation spectrometer were used in the analysis of the K X-rays and beta particles respectively. A half-life of (0.98 ± 0.03) min was associated with the K X-rays from technetium. A Kurie plot of the coincidence beta spectrum revealed at least three beta groups with end-point energies of (2.19 ± 0.19) MeV, (1.64 ± 0.14) MeV and (1.04 ± 0.10) MeV.

  4. A Research Program for Fission Product/Dust Transport in HTGR’s

    SciTech Connect

    Loyalka, Sudarshan

    2016-02-01

    High and Very High Temperatures Gas Reactors (HTGRs/VHTRs) have five barriers to fission product (FP) release: the TRISO fuel coating, the fuel elements, the core graphite, the primary coolant system, and the reactor building. This project focused on measurements and computations of FP diffusion in graphite, FP adsorption on graphite and FP interactions with dust particles of arbitrary shape. Diffusion Coefficients of Cs and Iodine in two nuclear graphite were obtained by the release method and use of Inductively Coupled Plasma-Mass Spectroscopy (ICP-MS) and Instrumented Neutron Activation Analysis (INAA). A new mathematical model for fission gas release from nuclear fuel was also developed. Several techniques were explored to measure adsorption isotherms, notably a Knudsen Effusion Mass Spectrometer (KEMS) and Instrumented Neutron Activation Analysis (INAA). Some of these measurements are still in progress. The results will be reported in a supplemental report later. Studies of FP interactions with dust and shape factors for both chain-like particles and agglomerates over a wide size range were obtained through solutions of the diffusion and transport equations. The Green's Function Method for diffusion and Monte Carlo technique for transport were used, and it was found that the shape factors are sensitive to the particle arrangements, and that diffusion and transport of FPs can be hindered. Several journal articles relating to the above work have been published, and more are in submission and preparation.

  5. Fission Product Release and Survivability of UN-Kernel LWR TRISO Fuel

    SciTech Connect

    Besmann, Theodore M; Ferber, Mattison K; Lin, Hua-Tay

    2014-01-01

    A thermomechanical assessment of the LWR application of TRISO fuel with UN kernels was performed. Fission product release under operational and transient temperature conditions was determined by extrapolation from range calculations and limited data from irradiated UN pellets. Both fission recoil and diffusive release were considered and internal particle pressures computed for both 650 and 800 m diameter kernels as a function of buffer layer thickness. These pressures were used in conjunction with a finite element program to compute the radial and tangential stresses generated with a TRISO particle as a function of fluence. Creep and swelling of the inner and outer pyrolytic carbon layers were included in the analyses. A measure of reliability of the TRISO particle was obtained by measuring the probability of survival of the SiC barrier layer and the maximum tensile stress generated in the pyrolytic carbon layers as a function of fluence. These reliability estimates were obtained as functions of the kernel diameter, buffer layer thickness, and pyrolytic carbon layer thickness. The value of the probability of survival at the end of irradiation was inversely proportional to the maximum pressure.

  6. Fission products measured from highly-enriched uranium irradiated under 10B4C in a research reactor

    SciTech Connect

    Metz, Lori A.; Friese, Judah I.; Finn, Erin C.; Greenwood, Lawrence R.; Hines, Corey C.; King, Matthew D.; Wall, Donald E.

    2016-03-01

    Critical assemblies provide one method of achieving a fast neutron spectrum that is close to a 235U fission-energy neutron spectrum for nuclear data measurements. Previous work has demonstrated the use of a natural boron carbide capsule for spectral-tailoring in a mixed spectrum reactor as an alternate and complementary method for performing fission-energy neutron experiments. Previous fission products measurements showed that the neutron spectrum achievable with natural boron carbide was not as hard as what can be achieved with critical assemblies. New measurements performed with the Washington State University TRIGA reactor using a boron carbide capsule 96% enriched in 10B for irradiations resulted in a neutron spectrum very similar to a critical assembly and a pure 235U fission spectrum. The current work describes an experiment involving a highly-enriched uranium target irradiated under the new 10B4C capsule. Fission product yields were measured following radiochemical separations and are presented here. Reactor dosimetry measurements for characterizing neutron spectra and fluence for the enriched boron carbide capsule and critical assemblies are also discussed.

  7. Comparison of fission product release predictions using PARFUME with results from the AGR-1 safety tests

    DOE PAGES

    Collin, Blaise P.; Petti, David A.; Demkowicz, Paul A.; ...

    2016-04-07

    Safety tests were conducted on fuel compacts from AGR-1, the first irradiation experiment of the Advanced Gas Reactor (AGR) Fuel Development and Qualification program, at temperatures ranging from 1600 to 1800 °C to determine fission product release at temperatures that bound reactor accident conditions. The PARFUME (PARticle FUel ModEl) code was used to predict the release of fission products silver, cesium, strontium, and krypton from fuel compacts containing tristructural isotropic (TRISO) coated particles during 15 of these safety tests. Comparisons between PARFUME predictions and post-irradiation examination results of the safety tests were conducted on two types of AGR-1 compacts: compactsmore » containing only intact particles and compacts containing one or more particles whose SiC layers failed during safety testing. In both cases, PARFUME globally over-predicted the experimental release fractions by several orders of magnitude: more than three (intact) and two (failed SiC) orders of magnitude for silver, more than three and up to two orders of magnitude for strontium, and up to two and more than one orders of magnitude for krypton. The release of cesium from intact particles was also largely over-predicted (by up to five orders of magnitude) but its release from particles with failed SiC was only over-predicted by a factor of about 3. These over-predictions can be largely attributed to an over-estimation of the diffusivities used in the modeling of fission product transport in TRISO-coated particles. The integral release nature of the data makes it difficult to estimate the individual over-estimations in the kernel or each coating layer. Nevertheless, a tentative assessment of correction factors to these diffusivities was performed to enable a better match between the modeling predictions and the safety testing results. The method could only be successfully applied to silver and cesium. In the case of strontium, correction factors could not be assessed

  8. Comparison of fission product release predictions using PARFUME with results from the AGR-1 safety tests

    SciTech Connect

    Collin, Blaise P.; Petti, David A.; Demkowicz, Paul A.; Maki, John T.

    2016-04-07

    Safety tests were conducted on fuel compacts from AGR-1, the first irradiation experiment of the Advanced Gas Reactor (AGR) Fuel Development and Qualification program, at temperatures ranging from 1600 to 1800 °C to determine fission product release at temperatures that bound reactor accident conditions. The PARFUME (PARticle FUel ModEl) code was used to predict the release of fission products silver, cesium, strontium, and krypton from fuel compacts containing tristructural isotropic (TRISO) coated particles during 15 of these safety tests. Comparisons between PARFUME predictions and post-irradiation examination results of the safety tests were conducted on two types of AGR-1 compacts: compacts containing only intact particles and compacts containing one or more particles whose SiC layers failed during safety testing. In both cases, PARFUME globally over-predicted the experimental release fractions by several orders of magnitude: more than three (intact) and two (failed SiC) orders of magnitude for silver, more than three and up to two orders of magnitude for strontium, and up to two and more than one orders of magnitude for krypton. The release of cesium from intact particles was also largely over-predicted (by up to five orders of magnitude) but its release from particles with failed SiC was only over-predicted by a factor of about 3. These over-predictions can be largely attributed to an over-estimation of the diffusivities used in the modeling of fission product transport in TRISO-coated particles. The integral release nature of the data makes it difficult to estimate the individual over-estimations in the kernel or each coating layer. Nevertheless, a tentative assessment of correction factors to these diffusivities was performed to enable a better match between the modeling predictions and the safety testing results. The method could only be successfully applied to silver and cesium. In the case of strontium, correction factors could not be assessed because

  9. On the role of energy separated in fission process, excitation energy and reaction channels effects in the isomeric ratios of fission product 135Xe in photofission of actinide elements

    NASA Astrophysics Data System (ADS)

    Thiep, Tran Duc; An, Truong Thi; Cuong, Phan Viet; Vinh, Nguyen The; Mishinski, G. V.; Zhemenik, V. I.

    2016-07-01

    In this work we present the isomeric ratio of fission product 135Xe in the photo-fission of actinide elements 232Th, 233U and 237Np induced by end-point bremsstrahlung energies of 13.5, 23.5 and 25.0 MeV which were determined by the method of inert gaseous flow. The data were analyzed, discussed and compared with the similar data from literature to examine the role of energy separated in fission process, excitation energy and reaction channels effects.

  10. Liquid water production from atmospheric sources

    NASA Astrophysics Data System (ADS)

    Matthews, John D.; Clarke, Norman P.

    1991-02-01

    The purpose of this effort was to assess the feasibility of developing a desiccant system to produce potable water from atmospheric sources that is compatible with military constraints. Goals were: (1) to examine desiccant technology, investigate methods of using available desiccants to collect atmospheric moisture, (2) develop a conceptual model of a desiccant water production system, and (3) develop a mathematical model to simulate the operation of the conceptual model. Results show that a desiccant system can produce large quantities of potable water using relatively small amounts of fuel for heat and fan power. The focus of this project was using a liquid desiccant (such as triethylene glycol) in an absorption-distillation cycle. This report documents the theoretical analysis of a hypothetical liquid desiccant based system for producing liquid water through collection of atmospheric moisture. Estimates are made of cost, weight and water production rate for the hypothetical system.

  11. Wet deposition of fission-product isotopes to North America from the Fukushima Dai-ichi incident, March 2011

    USGS Publications Warehouse

    Wetherbee, Gregory A.; Gay, David A.; Debey, Timothy M.; Lehmann, Christopher M.B.; Nilles, Mark A.

    2012-01-01

    Using the infrastructure of the National Atmospheric Deposition Program (NADP), numerous measurements of radionuclide wet deposition over North America were made for 167 NADP sites before and after the Fukushima Dai-ichi Nuclear Power Station incident of March 12, 2011. For the period from March 8 through April 5, 2011, wet-only precipitation samples were collected by NADP and analyzed for fission-product isotopes within whole-water and filterable solid samples by the United States Geological Survey using gamma spectrometry. Variable amounts of 131I, 134Cs, or 137Cs were measured at approximately 21% of sampled NADP sites distributed widely across the contiguous United States and Alaska. Calculated 1- to 2-week individual radionuclide deposition fluxes ranged from 0.47 to 5100 Becquerels per square meter during the sampling period. Wet deposition activity was small compared to measured activity already present in U.S. soil. NADP networks responded to this complex disaster, and provided scientifically valid measurements that are comparable and complementary to other networks in North America and Europe.

  12. Laboratory-Scale Bismuth Phosphate Extraction Process Simulation To Track Fate of Fission Products

    SciTech Connect

    Serne, R. JEFFREY; Lindberg, Michael J.; Jones, Thomas E.; Schaef, Herbert T.; Krupka, Kenneth M.

    2007-02-28

    Recent field investigation that collected and characterized vadose zone sediments from beneath inactive liquid disposal facilities at the Hanford 200 Areas show lower than expected concentrations of a long-term risk driver, Tc-99. Therefore laboratory studies were performed to re-create one of the three processes that were used to separate the plutonium from spent fuel and that created most of the wastes disposed or currently stored in tanks at Hanford. The laboratory simulations were used to compare with current estimates based mainly on flow sheet estimates and spotty historical data. Three simulations of the bismuth phosphate precipitation process show that less that 1% of the Tc-99, Cs-135/137, Sr-90, I-129 carry down with the Pu product and thus these isotopes should have remained within the metals waste streams that after neutralization were sent to single shell tanks. Conversely, these isotopes should not be expected to be found in the first and subsequent cycle waste streams that went to cribs. Measurable quantities (~20 to 30%) of the lanthanides, yttrium, and trivalent actinides (Am and Cm) do precipitate with the Pu product, which is higher than the 10% estimate made for current inventory projections. Surprisingly, Se (added as selenate form) also shows about 10% association with the Pu/bismuth phosphate solids. We speculate that the incorporation of some Se into the bismuth phosphate precipitate is caused by selenate substitution into crystal lattice sites for the phosphate. The bulk of the U daughter product Th-234 and Np-237 daughter product Pa-233 also associate with the solids. We suspect that the Pa daughter products of U (Pa-234 and Pa-231) would also co-precipitate with the bismuth phosphate induced solids. No more than 1 % of the Sr-90 and Sb-125 should carry down with the Pu product that ultimately was purified. Thus the current scheme used to estimate where fission products end up being disposed overestimates by one order of magnitude the

  13. IMPACT OF FISSION PRODUCTS IMPURITY ON THE PLUTONIUM CONTENT IN PWR MOX FUELS

    SciTech Connect

    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.

  14. Mass spectrometry studies of fission product behavior: 2, Gas phase species

    SciTech Connect

    Blackburn, P.E.; Johnson, C.E.

    1987-01-01

    Revaporization of fission products from reactor system surfaces has become a complicating factor in source term definition. Critical to this phenomena is understanding the nature and behavior of the vapor phase species. This study characterizes the stability of the CsI . CsOH vapor phase complex. Vapor pressures were measured with a mass spectrometer. Thermodynamic data were obtained for CsOH(g), Cs/sub 2/(OH)/sub 2/(g), CsI(g), Cs/sub 2/I/sub 2/(g) and CsI . CsOH(g). Activity coefficients were derived for the CsI-CsOH system. The relative ionization cross section of CsOH is about ten times the cross section of CsI(g). CsI . CsOH fragments to Cs/sub 2/OH/sup +/ and an iodine atom. 17 refs., 4 figs., 6 tabs.

  15. Method and device for fabricating dispersion fuel comprising fission product collection spaces

    DOEpatents

    Shaber, Eric L; Fielding, Randall S

    2015-05-05

    A method of fabricating a nuclear fuel comprising a fissile material, one or more hollow microballoons, a phenolic resin, and metal matrix. The fissile material, phenolic resin and the one or more hollow microballoons are combined. The combined fissile material, phenolic resin and the hollow microballoons are heated sufficiently to form at least some fissile material carbides creating a nuclear fuel particle. The resulting nuclear fuel particle comprises one or more fission product collection spaces. In a preferred embodiment, the fissile material, phenolic resin and the one or more hollow microballoons are combined by forming the fissile material into microspheres. The fissile material microspheres are then overcoated with the phenolic resin and microballoon. In another preferred embodiment, the fissile material, phenolic resin and the one or more hollow microballoons are combined by overcoating the microballoon with the fissile material, and phenolic resin.

  16. Fission product partitioning in aerosol release from simulated spent nuclear fuel

    NASA Astrophysics Data System (ADS)

    Di Lemma, F. G.; Colle, J. Y.; Rasmussen, G.; Konings, R. J. M.

    2015-10-01

    Aerosols created by the vaporization of simulated spent nuclear fuel (simfuel) were produced by laser heating techniques and characterised by a wide range of post-analyses. In particular attention has been focused on determining the fission product behaviour in the aerosols, in order to improve the evaluation of the source term and consequently the risk associated with release from spent fuel sabotage or accidents. Different simulated spent fuels were tested with burn-up up to 8 at. %. The results from the aerosol characterisation were compared with studies of the vaporization process by Knudsen Effusion Mass Spectrometry and thermochemical equilibrium calculations. These studies permit an understanding of the aerosol gaseous precursors and the gaseous reactions taking place during the aerosol formation process.

  17. LOW-FIDELITY CROSS SECTION COVARIANCES FOR 219 FISSION PRODUCTS IN THE FIRST NEUTRON REGION.

    SciTech Connect

    PIGNI,M.T.; HERMAN, M.; OBLOZINSKY, P.; ROCHMAN, D.

    2007-04-27

    An extensive set of covariances for neutron cross sections in the energy range 5 keV-20 MeV has been developed to provide initial, low-fidelity but consistent uncertainty data for nuclear criticality safety applications. The methodology for the determination of such covariances combines the nuclear reaction model code EMPIRE, which calculates sensitivity to nuclear reaction model parameters, and the Bayesian code KALMAN to propagate uncertainty of the model parameters to cross sections. Taking into account the large scale of the project (219 fission products), only partial reference to experimental data has been made. Therefore, the covariances are, to a large extent, derived from the perturbation of several critical model parameters selected through the sensitivity analysis. These parameters define optical potential, level densities and pre-equilibrium emission. This work represents the first attempt ever to generate nuclear data covariances on such a scale.

  18. Fission Product Release from Molten U/Al Alloy Fuel: A Vapor Transpiration Model

    SciTech Connect

    Whitkop, P.G.

    2001-06-26

    This report describes the application of a vapor transportation model to fission product release data obtained for uranium/aluminum alloy fuel during early Oak Ridge fuel melt experiments. The Oak Ridge data validates the vapor transpiration model and suggests that iodine and cesium are released from the molten fuel surface in elemental form while tellurium and ruthenium are released as oxides. Cesium iodide is postulated to form in the vapor phase outside of the fuel matrix. Kinetic data indicates that cesium iodide can form from Cs atoms and diatomic iodine in the vapor phase. Temperatures lower than those capable of melting fuel are necessary in order to maintain a sufficient I2 concentration. At temperatures near the fuel melting point, cesium can react with iodine atoms to form CsI only on solid surfaces such as aerosols.

  19. First-principles study of defects and fission product behavior in uranium diboride

    NASA Astrophysics Data System (ADS)

    Jossou, Ericmoore; Oladimeji, Dotun; Malakkal, Linu; Middleburgh, Simon; Szpunar, Barbara; Szpunar, Jerzy

    2017-10-01

    A Systematic study of defects and incorporation of xenon (Xe) and zirconium (Zr) fission products in uranium diboride (UB2) has been investigated using density functional theory (DFT) calculations as implemented in Quantum ESPRESSO code. The incorporation and solution energies show that both FPs (Xe and Zr) are most stable in U vacancies with Zr being more stable than Xe. A volume expansion is observed as the concentration of Xe increases in the fuel matrix while Zr incorporation leads to a contraction. Bader charge analysis is used to establish the formation of Zr-B ionic/covalent bond due to large electron transfer observed while there is only a weak electronic interaction between Xe and the UB2 lattice. Finally, using climbing-image nudged elastic band calculation, we found that the energy barrier of U in UB2 is 0.08 eV higher than B migration energy.

  20. Nuclear structure and shapes from prompt gamma ray spectroscopy of fission products

    SciTech Connect

    Ahmad, I.; Morss, L.R.; Durell, J.L.

    1996-10-01

    Many nuclear shape phenomena are predicted to occur in neutron-rich nuclei. The best source for the production of these nuclides is the spontaneous fission which produces practically hundreds of nuclides with yields of greater than 0.1 % per decay. Measurements of coincident gamma rays with large Ge arrays have recently been made to obtain information on nuclear structures and shapes of these neutron- rich nuclei. Among the important results that have been obtained from such measurements are octupole correlations in Ba isotopes, triaxial shapes in Ru nuclei, two-phonon vibrations in {sup 106}Mo and level lifetimes and quadrupole moments in Nd isotopes and A=100 nuclei. These data have been used to test theoretical models.

  1. Cherenkov light detection as a velocity selector for uranium fission products at intermediate energies

    NASA Astrophysics Data System (ADS)

    Yamaguchi, T.; Enomoto, A.; Kouno, J.; Yamaki, S.; Matsunaga, S.; Suzaki, F.; Suzuki, T.; Abe, Y.; Nagae, D.; Okada, S.; Ozawa, A.; Saito, Y.; Sawahata, K.; Kitagawa, A.; Sato, S.

    2014-12-01

    The in-flight particle separation capability of intermediate-energy radioactive ion (RI) beams produced at a fragment separator can be improved with the Cherenkov light detection technique. The cone angle of Cherenkov light emission varies as a function of beam velocity. This can be exploited as a velocity selector for secondary beams. Using heavy ion beams available at the HIMAC synchrotron facility, the Cherenkov light angular distribution was measured for several thin radiators with high refractive indices (n = 1.9 2.1). A velocity resolution of 10-3 was achieved for a 56Fe beam with an energy of 500 MeV/nucleon. Combined with the conventional rigidity selection technique coupled with energy-loss analysis, the present method will enable the efficient selection of an exotic species from huge amounts of various nuclides, such as uranium fission products at the BigRIPS fragment separator located at the RI Beam Factory.

  2. Atmospheric trident production for probing new physics

    NASA Astrophysics Data System (ADS)

    Ge, Shao-Feng; Lindner, Manfred; Rodejohann, Werner

    2017-09-01

    We propose to use atmospheric neutrinos as a powerful probe of new physics beyond the Standard Model via neutrino trident production. The final state with double muon tracks simultaneously produced from the same vertex is a distinctive signal at large Cherenkov detectors. We calculate the expected event numbers of trident production in the Standard Model. To illustrate the potential of this process to probe new physics we obtain the sensitivity on new vector/scalar bosons with coupling to muon and tau neutrinos.

  3. Isolation and Purification of the Xenon Fraction of 252Cf Spontaneous Fission Products for the Production of Radio Xenon Calibration Standards

    SciTech Connect

    McGrath, Christopher A.

    2015-04-01

    The presence of radioactive xenon isotopes indicates that fission events have occurred, and is used to help enforce the Comprehensive Test Ban Treaty. Idaho National Laboratory (INL) produces 135Xe, 133mXe, 133Xe, and 131mXe standards used for the calibration and testing of collection equipment and analytical techniques used to monitor radio xenon emissions. At INL, xenon is produced and collected as one of several spontaneous fission products from a 252Cf source. Further chromatographic purification of the fission gases ensures the separations of the xenon fraction for selective collection. An explanation of the fission gas collection, separation and purification is presented. Additionally, the range of 135Xe to 133Xe ratio that can be isolated is explained. This is an operational update on the work introduced previously, now that it is in operation and has been recharged with a second 252Cf source.

  4. DFT-based prediction of fission product sorption on carbon structures under O2 ingress conditions

    NASA Astrophysics Data System (ADS)

    Londono-Hurtado, Alejandro; Szlufarska, Izabela; Morgan, Dane

    2013-06-01

    An isotherm based model for the prediction of Cs sorption on the carbon components of a High Temperature Reactor (HTR) under O2 ingress conditions is presented. Isotherms are derived from a thermodynamic model based on binding energies calculated using Density Functional Theory (DFT). The DFT derived isotherms are compared with isotherms obtained from experimental calculations and sources of discrepancies are discussed. A DFT only model and a second model combining DFT and experimental calculations are used to predict fission product inventories in a HTR vessel during O2 ingress conditions. Results suggest that the carbon type (i.e. graphitic vs. amorphous) plays a central role on fission product sorption and release. During normal reactor conditions (T around 1400 K, low P) graphitic carbon will absorb a small percentage of a monolayer of Cs, while amorphous carbon will be approximately saturated at an entire monolayer of Cs. Results also indicate that, for the case of O2 ingress to the reactor's vessel, the Cs will form Cs2O. In the case of graphitic carbon, the Cs2O will bind more weakly than Cs, leading to Cs release in the form of Cs2O during O ingress. However, the weak binding of Cs to graphite means that only small release is expected. In the case of amorphous carbon, Cs2O binds almost as strongly Cs, and so no significant change in Cs absorbed to the amorphous carbon is predicted, although the form of the absorbed Cs is predicted to be Cs2O. For the case of low release conditions, consistent with modern TRISO fuels, the core will adsorb the entire Cs inventory at normal operating temperatures. However, for high Cs release conditions, consistent with older TRISO fuels, the surface sites on the core will be saturated and most of the Cs will remain in gas form or plate out on other surfaces.

  5. Use of the linear accelerator for incinerating the fission products of /sup 137/Cs and /sup 90/Sr

    SciTech Connect

    Takahashi, H; Mizoo, N; Steinberg, M

    1980-07-01

    Transmutation of fission products /sup 137/Cs and /sup 90/Sr using the neutron produced by high energy proton collision with heavy nuclei were investigated. Because of the small thermal neutron cross section for (n,..gamma..) reaction of /sup 137/Cs (0.1 barn), a high neutron flux of 10/sup 17/ n/cm/sup 2/ sec is required to transmute /sup 137/Cs at a rate ten times faster than the natural decay. This range of high flux is attainable in the spallation reaction of high energy proton beam interact with liquid Pb target. The neutronic calculation by using NMTC, HIST3D, EPR, TAPEMAKER and ANISN codes indicates that the spallation neutron can transmute 222 kg /sup 137/Cs and 155 kg /sup 90/Sr fission products per year (at a rate of 10 and 30 times faster than their natural decay rate) by running a 300 mA, 1.5 GeV proton beam. Thus, if we transmute these fission products, just after a burning cycle, this accelerator can transmute these fission products produced in five or six 1000 MWe power plants.

  6. Assessment of improved fission-product transport models in VICTORIA against the ORNL HI and VI tests

    SciTech Connect

    Domagala, P.; Rest, J.; Zawadzki, S.A.

    1991-01-01

    New models for the release of fission-products from fuel have recently been incorporated into a comprehensive code, VICTORIA, for the prediction of radionuclide behavior under severe reactor accident conditions as an alternative to a simple Booth diffusion calculation. It is widely known that the Booth model has severe limitations when used under conditions of changing temperature and power. A new transport model based on a two node diffusive flow formulation has been implemented into VICTORIA. In addition to the diffusive flow model, other mechanisms such as grain growth, grain boundary sweeping and intergranular bubble behavior are taken into account. These physically based models focus on fission-product behavior in intact fuel geometries. While the VICTORIA program is primarily concerned with the behavior of severely degraded fuel geometries, the capability for accurately characterizing fission-product release from intact fuel must be demonstrated before other geometries can be reliably modeled. Results of VICTORIA simulations are compared with the results of in-cell heating tests on irradiated fuel. The fission-product transport models involved in these simulations are assessed and their predictive capability examined. 10 refs., 7 figs., 2 tabs.

  7. Thermodynamics of fission products in dispersion fuel designs - first principles modeling of defect behavior in bulk and at interfaces

    SciTech Connect

    Liu, Xiang-yand; Uberuaga, Blas P; Nerikar, Pankaj; Sickafus, Kurt E; Stanek, Chris R

    2009-01-01

    Density functional theory (DFT) calculations of fission product (Xe, Sr, and Cs) incorporation and segregation in alkaline earth metal oxides, HfO{sub 2} and UO{sub 2} oxides, and the MgO/(U, Hf, Ce)O{sub 2} interfaces have been carried out. In the case of UO{sub 2}, the calculations were performed using spin polarization and with a Hubbard U term characterizing the on-sit Coulomb repulsion between the localized 5f electrons. The fission product solution energies in bulk UO{sub 2{+-}x} have been calculated as a function of non-stoichiometry x, and were compared to that in MgO. These calculations demonstrate that the fission product incorporation energies in MgO are higher than in HfO{sub 2}. However, this trend is reversed or reduced for alkaline earth oxides with larger cation sizes. The solution energies of fission products in MgO are substantially higher than in UO{sub 2{+-}x}, except for the case of Sr in the hypostoichiometric case. Due to size effects, the thermodynamic driving force of segregation for Xe and Cs from bulk MgO to the MgO/fluorite interface is strong. However, this driving force is relatively weak for Sr.

  8. Preliminary investigations on the use of uranium silicide targets for fission Mo-99 production

    SciTech Connect

    Cols, H.; Cristini, P.; Marques, R.

    1997-08-01

    The National Atomic Energy Commission (CNEA) of Argentine Republic owns and operates an installation for production of molybdenum-99 from fission products since 1985, and, since 1991, covers the whole national demand of this nuclide, carrying out a program of weekly productions, achieving an average activity of 13 terabecquerel per week. At present they are finishing an enlargement of the production plant that will allow an increase in the volume of production to about one hundred of terabecquerel. Irradiation targets are uranium/aluminium alloy with 90% enriched uranium with aluminium cladding. In view of international trends held at present for replacing high enrichment uranium (HEU) for enrichment values lower than 20 % (LEU), since 1990 the authors are in contact with the RERTR program, beginning with tests to adapt their separation process to new irradiation target conditions. Uranium silicide (U{sub 3}Si{sub 2}) was chosen as the testing material, because it has an uranium mass per volume unit, so that it allows to reduce enrichment to a value of 20%. CNEA has the technology for manufacturing miniplates of uranium silicide for their purposes. In this way, equivalent amounts of Molybdenum-99 could be obtained with no substantial changes in target parameters and irradiation conditions established for the current process with Al/U alloy. This paper shows results achieved on the use of this new target.

  9. Exploratory study of fission product yield determination from photofission of 239Pu at 11 MeV with monoenergetic photons

    NASA Astrophysics Data System (ADS)

    Bhike, Megha; Tornow, W.; Krishichayan, Tonchev, A. P.

    2017-02-01

    Measurements of fission product yields play an important role for the understanding of fundamental aspects of the fission process. Recently, neutron-induced fission product-yield data of 239Pu at energies below 4 MeV revealed an unexpected energy dependence of certain fission fragments. In order to investigate whether this observation is prerogative to neutron-induced fission, a program has been initiated to measure fission product yields in photoinduced fission. Here we report on the first ever photofission product yield measurement with monoenergetic photons produced by Compton back-scattering of FEL photons. The experiment was performed at the High-Intensity Gamma-ray Source at Triangle Universities Nuclear Laboratory on 239Pu at Eγ=11 MeV. In this exploratory study the yield of eight fission products ranging from 91Sr to 143Ce has been obtained.

  10. The OMI Atmospheric Science Data Products

    NASA Astrophysics Data System (ADS)

    Johnson, J. E.; Ahmad, S. P.; Levelt, P. F.; Bhartia, P. K.; Hilsenrath, E.; Leppelmeier, G. W.

    2003-12-01

    The Ozone Monitoring Instrument (OMI), will provide measurements in the UV and Visible spectral regions (1560 wavelength bands between 270 and 500 nm with approximately 0.5 nm spectral resolution). OMI will continue the long-term Total Ozone Mapping Spectrometer (TOMS) column ozone record and will focus on monitoring the ozone layer, ozone depleting trace gases (BrO and OClO), atmospheric pollutants (tropospheric ozone, NO2, SO2, and HCHO), clouds and aerosols characteristics, and surface spectral UV irradiance and erythemal surface UV-B flux. OMI is a contribution of the Netherlands Agency for Aerospace Programs (NIVR) in collaboration with the Finnish Meteorological Institute (FMI), to NASA's Aura mission. It will be flown on the Aura spacecraft (early 2004) in a sun-synchronous polar orbit with equator crossing time approximately at 1:38 p.m in the ascending mode. The standard atmospheric chemistry and dynamics products derived from OMI, and from the other two Aura sensors, the High Resolution Dynamics Limb Sounder (HIRDLS) and the Microwave Limb Sounder (MLS), will be archived at the NASA GES DAAC. OMI atmospheric data products will provide continuity to the over 30 year long-term ozone data records obtained from the heritage atmospheric data missions including Nimbus-4 BUV and Nimbus-7 SBUV, and a series of TOMS instruments, also archived at the NASA GES DAAC. The standard satellite data sets, as well as regional subsets, related ancillary data sets, and data analysis tools are freely available to the public for the Earth System Science studies, environmental applications, and educational use. This presentation will provide an overview of the OMI instrument, data processing, data products, and the data services provided by the NASA GES DAAC's Upper Atmosphere Data Support team to the user in the areas of accessing data products, documentation, browse, and data analysis software.

  11. The use of gamma spectrometry in the determination of fission products migration in irradiated fuel

    SciTech Connect

    2015-07-01

    Non destructive examinations realized in hot cells of LECA STAR facility give main data on irradiated fuel rods and pins. Among those examinations, gamma spectrometry allows access to fuel, inside the cladding, thanks to gamma rays of fission products such as {sup 137}Cs, {sup 154}Eu coming from pellets... From those gamma scannings we can detect the position and the length of the fuel column and of its pellets, calculate local burnup.. In the database of our lab we have already such gamma scannings on hundreds of rods or pins with different fuels, claddings and irradiations conditions (under nominal or non nominal). We have detected that in specific cases, an unusual shape of the {sup 137}Cs scanning (distribution quite different from those of {sup 154}Eu) can be explained by the migration of this isotope, moving to the cold sides of the pellet. This phenomenon is mainly associated with an increasing of the pellet's temperature. Based on our observations, we have developed a quantitative approach of the changes on the {sup 137}Cs scannings through the calculation of appropriate 'indicators'. Those calculations allow us to be able to localize, quantify and compare the {sup 137}Cs migration all along rods or pins. Those migration results are so quickly and easily achievable from gamma measurements and can then be easily correlated to other observations realized with destructive examinations, puncturing and calculations, already realized or to come. Because such a migration is the result of temperature increasing in the pellets, our indicators can be directly associated with this local temperature. In perspective, thermically activated phenomena such as geometrical changes in the shape of the pellets, fission gas release... can also indirectly be deduced from our indicators. (authors)

  12. Energy Dependence of Neutron-Induced Fission Product Yields of 235U, 238U and 239Pu Between 0.5 and 14.8 MeV

    NASA Astrophysics Data System (ADS)

    Gooden, Matthew; Tornow, Werner; Tonchev, Anton; Vieira, Dave; Wilhelmy, Jerry; Arnold, Charles; Fowler, Malcolm; Stoyer, Mark

    2014-09-01

    Under a joint collaboration between TUNL-LANL-LLNL, a set of absolute fission product yield measurements have been performed. The energy dependence of a number of cumulative fission products between 0.5 and 14.8 MeV have been measured using quasi-monoenergetic neutron beams for three actinide targets, 235U, 238U and 239Pu, between 0.5 and 14.8 MeV. The FPYs were measured by a combination of activation utilizing specially designed dual-fission chambers and γ-ray counting. The dual-fission chambers are back-to-back ionization chambers encasing a target with thin deposits of the same target isotope in each chamber. This method allows for the direct measurement of the fission rate in the activation target with no reference to the fission cross-section, reducing uncertainties. γ-ray counting was performed on well-shield HPGe detectors over a period of 2 months per activation to properly identify fission products. Reported are absolute cumulative fission product yields for incident neutron energies of 0.5, 1.37, 2.4, 4.6 and 14.8 MeV.

  13. Triplet Separation Drives Singlet Fission after Femtosecond Correlated Triplet Pair Production in Rubrene.

    PubMed

    Breen, Ilana; Tempelaar, Roel; Bizimana, Laurie A; Kloss, Benedikt; Reichman, David R; Turner, Daniel B

    2017-08-30

    Singlet fission, a multistep molecular process in which one photon generates two triplet excitons, holds great technological promise. Here, by applying a combination of transient transmittance and two-dimensional electronic spectroscopy with 5 fs laser pulses, we resolve the full set of fission steps before the onset of spin dephasing. In addition to its role as a viable singlet fission material, single-crystalline rubrene is selected because its energetics and transition dipole alignment uniquely allow for the unambiguous identification of the various fission steps through their contributions to distinct spectroscopic features. The measurements reveal that the neighboring correlated triplet pair achieves its maximum population within 20 fs. Subsequent growth of the triplet signal on picosecond time scales is attributable to spatial separation of the triplets, proceeding nonadiabatically through weakly coupled but near-resonant states. As such, we provide evidence in crystalline rubrene for a singlet fission step that, until now, has not been convincingly observed.

  14. Spallation and fission products in the (p+ 179Hf) and (p+ natHf) reactions

    NASA Astrophysics Data System (ADS)

    Karamian, S. A.; Ur, C. A.; Adam, J.; Kalinnikov, V. G.; Lebedev, N. A.; Vostokin, G. K.; Collins, C. B.; Popescu, I. I.

    2009-03-01

    Production of Hf and Lu high-spin isomers has been experimentally studied in spallation reactions induced by intermediate energy protons. Targets of enriched 179Hf (91%) and natHf were bombarded with protons of energy in the range from 90 to 650 MeV provided by the internal beam of the Dubna Phasotron synchrocyclotron. The activation yields of the reaction products were measured by using the γ-ray spectroscopy and radiochemistry methods. The production cross-sections obtained for the 179m2Hf, 178m2Hf and 177mLu isomers are similar to the previously measured values from the spallation of Ta, Re and W targets. Therefore, the reactions involving emission of only a few nucleons, like (p,p'), (p,p'n) and (p,2pn), can transfer high enough angular momentum to the final residual nuclei with reasonable large cross-sections. A significant gain in the isomeric yields was obtained when enriched 179Hf targets were used. The mass distribution of the residual nuclei was measured over a wide range of masses and the fission-to-spallation ratio could be deduced as a function of the projectile energy. Features of the reaction mechanism are briefly discussed.

  15. Feasibility of 99Mo production by proton-induced fission of 232Th

    NASA Astrophysics Data System (ADS)

    Abbas, Kamel; Holzwarth, Uwe; Simonelli, Federica; Kozempel, Jan; Cydzik, Izabela; Bulgheroni, Antonio; Cotogno, Giulio; Apostolidis, Christos; Bruchertseifer, Frank; Morgenstern, Alfred

    2012-05-01

    The current global crisis in supply of the medical isotope generator 99Mo/99mTc has triggered much research into alternative non-reactor based production methods for 99Mo including innovative radionuclide production techniques using ion accelerators. A novel method is presented here that has thus far not been considered: 232Th is used as target material to produce carrier-free 99Mo for 99Mo/99mTc generators by proton-induced fission (232Th (p, f) 99Mo). The thick target yields of 99Mo are estimated as 3.6 MBq/μA·h and 21 MBq/μA·h for proton energies of 22 MeV and 40 MeV, respectively, energies that are available from many cyclotrons. With respect to 99Mo reactor based methods using uranium targets, the presented concept using 232Th does not pose proliferation concerns, transport of highly radioactive target materials can be reduced and unused cyclotron capacities could be exploited. Radiochemical target processing could be based on existing technologies of extraction of 99Mo from reactor irradiated 235U. The presented method could be used for co-production of other radioisotopes of medical interest such as 131I.

  16. Determination of long-lived fission products and actinides in Savannah River site HLW sludge and glass for waste acceptance

    SciTech Connect

    Bibler, N.E.; Boyce, W.T.; Coleman, C.J.

    1997-10-01

    Savannah River Site (SRS) is currently immobilizing the radioactive, caustic, high-level waste sludge in Tank 51 into a borosilicate glass for disposal in a geologic repository. A requirement for repository acceptance is that SRS report the concentrations of certain fission product and actinide radionuclides in the glass. This paper presents measurements of many of these concentrations in both Tank 51 sludge and the final glass. The radionuclides were measured by inductively coupled plasma - mass spectrometry and {alpha}, {beta}, and {gamma} counting methods. Examples of the radionuclides are Sr-90, Cs-137, U-238, Pu-239, and Cm-244. Concentrations in the glass are 3.1 times lower due to dilution of the sludge with a nonradioactive glass forming frit in the vitrification process. Results also indicated that in both the sludge and glass the relative concentrations of the long lived fission products insoluble in caustic area in proportion to their yields from the fission of U-235 in the SRS reactors. This allowed the calculation of a fission yield scaling factor. This factor in addition to the sludge dilution factor can be used to estimate concentrations of waste acceptance radionuclides that cannot be measured in the glass.

  17. Yields of short-lived fission products produced following {sup 235}U(n{sub th},f)

    SciTech Connect

    Tipnis, S.V.; Campbell, J.M.; Couchell, G.P.; Li, S.; Nguyen, H.V.; Pullen, D.J.; Schier, W.A.; Seabury, E.H.; England, T.R.

    1998-08-01

    Measurements of gamma-ray spectra, following the thermal neutron fission of {sup 235}U have been made using a high purity germanium detector at the University of Massachusetts Lowell (UML) Van de Graaff facility. The gamma spectra were measured at delay times ranging from 0.2 s to nearly 10thinsp000 s following the rapid transfer of the fission fragments with a helium-jet system. On the basis of the known gamma transitions, forty isotopes have been identified and studied. By measuring the relative intensities of these transitions, the relative yields of the various precursor nuclides have been calculated. The results are compared with the recommended values listed in the ENDF/B-VI fission product data base (for the lifetimes and the relative yields) and those published in the Nuclear Data Sheets (for the beta branching ratios). This information is particularly useful for the cases of short-lived fission products with lifetimes of the order of fractions of a second or a few seconds. Independent yields of many of these isotopes have rather large uncertainties, some of which have been reduced by the present study. {copyright} {ital 1998} {ital The American Physical Society}

  18. Determination of relative krypton fission product yields from 14 MeV neutron induced fission of (238)U at the National Ignition Facility.

    PubMed

    Edwards, E R; Cassata, W S; Velsko, C A; Yeamans, C B; Shaughnessy, D A

    2016-11-01

    Precisely-known fission yield distributions are needed to determine a fissioning isotope and the incident neutron energy in nuclear security applications. 14 MeV neutrons from DT fusion at the National Ignition Facility induce fission in depleted uranium contained in the target assembly hohlraum. The fission yields of Kr isotopes (85m, 87, 88, and 89) are measured relative to the cumulative yield of (88)Kr and compared to previously tabulated values. The results from this experiment and England and Rider are in agreement, except for the (85m)Kr/(88)Kr ratio, which may be the result of incorrect nuclear data.

  19. Determination of relative krypton fission product yields from 14 MeV neutron induced fission of 238U at the National Ignition Facility

    NASA Astrophysics Data System (ADS)

    Edwards, E. R.; Cassata, W. S.; Velsko, C. A.; Yeamans, C. B.; Shaughnessy, D. A.

    2016-11-01

    Precisely-known fission yield distributions are needed to determine a fissioning isotope and the incident neutron energy in nuclear security applications. 14 MeV neutrons from DT fusion at the National Ignition Facility induce fission in depleted uranium contained in the target assembly hohlraum. The fission yields of Kr isotopes (85m, 87, 88, and 89) are measured relative to the cumulative yield of 88Kr and compared to previously tabulated values. The results from this experiment and England and Rider are in agreement, except for the 85mKr/88Kr ratio, which may be the result of incorrect nuclear data.

  20. Comparison of fission product release predictions using PARFUME with results from the AGR-1 safety tests

    SciTech Connect

    Blaise Collin

    2014-09-01

    Safety tests were conducted on fourteen fuel compacts from AGR-1, the first irradiation experiment of the Advanced Gas Reactor (AGR) Fuel Development and Qualification program, at temperatures ranging from 1600 to 1800°C to determine fission product release at temperatures that bound reactor accident conditions. The PARFUME (PARticle FUel ModEl) code was used to predict the release of fission products silver, cesium, strontium, and krypton from fuel compacts containing tristructural isotropic (TRISO) coated particles during the safety tests, and the predicted values were compared with experimental results. Preliminary comparisons between PARFUME predictions and post-irradiation examination (PIE) results of the safety tests show different trends in the prediction of the fractional release depending on the species, and it leads to different conclusions regarding the diffusivities used in the modeling of fission product transport in TRISO-coated particles: • For silver, the diffusivity in silicon carbide (SiC) might be over-estimated by a factor of at least 102 to 103 at 1600°C and 1700°C, and at least 10 to 102 at 1800°C. The diffusivity of silver in uranium oxy-carbide (UCO) might also be over-estimated, but the available data are insufficient to allow definitive conclusions to be drawn. • For cesium, the diffusivity in UCO might be over-estimated by a factor of at least 102 to 103 at 1600°C, 105 at 1700°C, and 103 at 1800°C. The diffusivity of cesium in SiC might also over-estimated, by a factor of 10 at 1600°C and 103 at 1700°C, based upon the comparisons between calculated and measured release fractions from intact particles. There is no available estimate at 1800°C since all the compacts heated up at 1800°C contain particles with failed SiC layers whose release dominates the release from intact particles. • For strontium, the diffusivity in SiC might be over-estimated by a factor of 10 to 102 at 1600 and 1700°C, and 102 to 103 at 1800°C. These

  1. Pyrene degradation by a Mycobacterium sp.: identification of ring oxidation and ring fission products.

    PubMed Central

    Heitkamp, M A; Freeman, J P; Miller, D W; Cerniglia, C E

    1988-01-01

    The degradation of pyrene, a polycyclic aromatic hydrocarbon containing four aromatic rings, by pure cultures of a Mycobacterium sp. was studied. Over 60% of [14C]pyrene was mineralized to CO2 after 96 h of incubation at 24 degrees C. High-pressure liquid chromatography analyses showed the presence of one major and at least six other metabolites that accounted for 95% of the total organic-extractable 14C-labeled residues. Analyses by UV, infrared, mass, and nuclear magnetic resonance spectrometry and gas chromatography identified both pyrene cis- and trans-4,5-dihydrodiols and pyrenol as initial microbial ring-oxidation products of pyrene. The major metabolite, 4-phenanthroic acid, and 4-hydroxyperinaphthenone and cinnamic and phthalic acids were identified as ring fission products. 18O2 studies showed that the formation of cis- and trans-4,5-dihydrodiols were catalyzed by dioxygenase and monooxygenase enzymes, respectively. This is the first report of the chemical pathway for the microbial catabolism of pyrene. PMID:3202634

  2. Primary system fission product release and transport: A state-of-the-art report to the committee on the safety of nuclear installations

    SciTech Connect

    Wright, A.L.

    1994-06-01

    This report presents a summary of the status of research activities associated with fission product behavior (release and transport) under severe accident conditions within the primary systems of water-moderated and water-cooled nuclear reactors. For each of the areas of fission product release and fission product transport, the report summarizes relevant information on important phenomena, major experiments performed, relevant computer models and codes, comparisons of computer code calculations with experimental results, and general conclusions on the overall state of the art. Finally, the report provides an assessment of the overall importance and knowledge of primary system release and transport phenomena and presents major conclusions on the state of the art.

  3. Deposition and distribution of Chernobyl fallout fission products and actinides in a Russian soil profile.

    PubMed

    Carbol, P; Solatie, D; Erdmann, N; Nylén, T; Betti, M

    2003-01-01

    In this article the distribution of fission products and actinides in a soil profile from Novo Bobovicky in Russia, which was contaminated due to the Chernobyl nuclear power plant accident, is described. The ground deposition of long-lived fission products determined by gamma-spectrometry was (recalculated to 26 April 1986) 1600 kBq (137)Cs/m(2), 900 kBq (134)Cs/m(2) and 60 kBq (125)Sb/m(2). Of these radionuclides (137)Cs shows the dominating activity at the present time. After 6.5 years 90% of the Cs and Sb activity was contained in the upper 4 cm. A (239,240)Pu ground deposition of 77.4+/-8.0 Bq/m(2) was determined by alpha-spectrometry. The (238)Pu/(239,240)Pu activity ratio of 0.30+/-0.03 and (241)Pu/(239,240)Pu activity ratio of 115+/-14 (in 1986) measured in the soil profile, indicates that the analysed Pu originates mainly from the Chernobyl accident. The average (234)U/(238)U activity ratio of 1.06+/-0.29 indicates that the uranium in this soil is dominated by naturally occurring uranium. The alpha- and beta-autoradiography revealed that the activity is mainly present in particulate form. It could further be observed that the spots containing alpha- or beta-activity originated from different particles. A comparison of alpha-autoradiography with the bulk Pu and Am activity showed that 92% of the alpha-activity was present as clearly detectable alpha-spots. The beta-active particles, located by beta-autoradiography were correlated with gamma-spectrometric measurements and contained only (137)Cs. These hot spots ranged from 0.02 to 0.15 Bq.It could be concluded that the vertical transport of (137)Cs and fuel fragments occurs mainly by movement of particles through the soil. It could also be concluded that the fuel fragments found, in this soil were depleted in respect to Cs, Sb and Eu. Comparison of the analysed (238)Pu/(239,240)Pu, (241)Pu/(239,240)Pu and (241)Am/(239,240)Pu ratios with the ratios calculated with ORIGEN-S code gave an estimate of the average

  4. Fission Product Gamma-Ray Line Pairs Sensitive to Fissile Material and Neutron Energy

    SciTech Connect

    Marrs, R E; Norman, E B; Burke, J T; Macri, R A; Shugart, H A; Browne, E; Smith, A R

    2007-11-15

    The beta-delayed gamma-ray spectra from the fission of {sup 235}U, {sup 238}U, and {sup 239}Pu by thermal and near-14-MeV neutrons have been measured for delay times ranging from 1 minute to 14 hours. Spectra at all delay times contain sets of prominent gamma-ray lines with intensity ratios that identify the fissile material and distinguish between fission induced by low-energy or high-energy neutrons.

  5. Instant release of fission products in leaching experiments with high burn-up nuclear fuels in the framework of the Euratom project FIRST- Nuclides

    NASA Astrophysics Data System (ADS)

    Lemmens, K.; González-Robles, E.; Kienzler, B.; Curti, E.; Serrano-Purroy, D.; Sureda, R.; Martínez-Torrents, A.; Roth, O.; Slonszki, E.; Mennecart, T.; Günther-Leopold, I.; Hózer, Z.

    2017-02-01

    The instant release of fission products from high burn-up UO2 fuels and one MOX fuel was investigated by means of leach tests. The samples covered PWR and BWR fuels at average rod burn-up in the range of 45-63 GWd/tHM and included clad fuel segments, fuel segments with opened cladding, fuel fragments and fuel powder. The tests were performed with sodium chloride - bicarbonate solutions under oxidizing conditions and, for one test, in reducing Ar/H2 atmosphere. The iodine and cesium release could be partially explained by the differences in sample preparation, leading to different sizes and properties of the exposed surface areas. Iodine and cesium releases tend to correlate with FGR and linear power rating, but the scatter of the data is significant. Although the gap between the fuel and the cladding was closed in some high burn-up samples, fissures still provide possible preferential transport pathways.

  6. Chemical states of fission products in irradiated (U 0.3Pu 0.7)C 1+ x fuel at high burn-ups

    NASA Astrophysics Data System (ADS)

    Agarwal, Renu; Venugopal, V.

    2006-12-01

    The chemical states of fission products have been theoretically determined for the irradiated carbide fuel of Fast Breeder Test Reactor (FBTR) at Kalpakkam, India, at different burn-ups. The SOLGASMIX-PV computer code was used to determine the equilibrium chemical composition of the fuel. The system was assumed to be composed of a gaseous phase at one atmosphere pressure, and various solid phases. The distribution of elements in these phases and their chemical states at different temperatures were calculated as a function of burn-up. The FBTR fuel, (U 0.3Pu 0.7)C 1+ x, was loaded with C/M values in the range, 1.03-1.06. The present calculations indicated that even for the lowest starting C/M of 1.03 in the FBTR fuel, the liquid metal phase of (U, Pu), should not appear at a burn-up as high as 150 GWd/t.

  7. Simulated fission product-SiC interaction in Triso-coated LEU or MEU HTGR fuel particles

    SciTech Connect

    Pearson, R.L.; Lindemer, T.B.; Beahm, E.C.

    1980-11-01

    Proliferation issues relating to the use of highly enriched uranium (HEU) have led to an evaluation of the fission product-SiC interaction problems that might arise if low enriched uranium (LEU) or medium enriched uranium (MEU) were used as fissile fuel in HTGR systems. Simulated Triso-coated UO/sub 2/, UC/sub 2/, and UO/sub 2//UC/sub 2/ particles mixed with varying amounts of Mo, Ru, Rh, Pd, Ag, and Cd were prepared. These fission products were chosen because, after full burnup, their concentrations are higher in LEU and MEU fuels than in HEU fuel. After the particles were heat treated in the laboratory, their behavior was examined by use of metallography, scanning electron microscopy, and electron microprobe x-ray analysis.

  8. Measurement of Airborne Fission Products in Chapel Hill, NC, USA from the Kukushima Dai-ichi Reactor Accident

    SciTech Connect

    MacMullin, S.; Giovanetti, G. K.; Green, M. P.; Henning, R.; Holmes, R.; Vorren, K.

    2012-01-01

    We present measurement results of airborne fission products in Chapel Hill, NC, USA, from 62 d following the March 11, 2011, accident at the Fukushima Dai-ichi nuclear power plant. Airborne particle samples were collected daily in air filters and radio-assayed with two high-purity germanium (HPGe) detectors. The fission products 131I and 137Cs were measured with maximum activity concentrations of 4.2 0.6 mBq/m3 and 0.42 0.07 mBq/m3 respectively. Additional activity from 131,132I, 134,136,137Cs and 132Te were measured in the same air filters using a low-background HPGe detector at the Kimballton Underground Research Facility (KURF).

  9. Next Generation Nuclear Plant Phenomena Identification and Ranking Tables (PIRTs) Volume 3: Fission-Product Transport and Dose PIRTs

    SciTech Connect

    Morris, Robert Noel

    2008-03-01

    This Fission Product Transport (FPT) Phenomena Identification and Ranking Technique (PIRT) report briefly reviews the high-temperature gas-cooled reactor (HTGR) FPT mechanisms and then documents the step-by-step PIRT process for FPT. The panel examined three FPT modes of operation: (1) Normal operation which, for the purposes of the FPT PIRT, established the fission product circuit loading and distribution for the accident phase. (2) Anticipated transients which were of less importance to the panel because a break in the pressure circuit boundary is generally necessary for the release of fission products. The transients can change the fission product distribution within the circuit, however, because temperature changes, flow perturbations, and mechanical vibrations or shocks can result in fission product movement. (3) Postulated accidents drew the majority of the panel's time because a breach in the pressure boundary is necessary to release fission products to the confinement. The accidents of interest involved a vessel or pipe break, a safety valve opening with or without sticking, or leak of some kind. Two generic scenarios were selected as postulated accidents: (1) the pressurized loss-of-forced circulation (P-LOFC) accident, and (2) the depressurized loss-of-forced circulation (D-LOFC) accidents. FPT is not an accident driver; it is the result of an accident, and the PIRT was broken down into a two-part task. First, normal operation was seen as the initial starting point for the analysis. Fission products will be released by the fuel and distributed throughout the reactor circuit in some fashion. Second, a primary circuit breach can then lead to their release. It is the magnitude of the release into and out of the confinement that is of interest. Depending on the design of a confinement or containment, the impact of a pressure boundary breach can be minimized if a modest, but not excessively large, fission product attenuation factor can be introduced into the

  10. Partition of actinides and fission products between metal and molten salt phases: Theory, measurement, and application to IFR pyroprocess development

    SciTech Connect

    Ackerman, J.P.; Johnson, T.R.

    1993-10-01

    The chemical basis of Integral Fast Reactor fuel reprocessing (pyroprocessing) is partition of fuel, cladding, and fission product elements between molten LiCl-KCl and either a solid metal phase or a liquid cadmium phase. The partition reactions are described herein, and the thermodynamic basis for predicting distributions of actinides and fission products in the pyroprocess is discussed. The critical role of metal-phase activity coefficients, especially those of rare earth and the transuranic elements, is described. Measured separation factors, which are analogous to equilibrium constants but which involve concentrations rather than activities, are presented. The uses of thermodynamic calculations in process development are described, as are computer codes developed for calculating material flows and phase compositions in pyroprocessing.

  11. Experimental investigations on the chemical state of solid fission-product elements in U3Si2

    NASA Astrophysics Data System (ADS)

    Ugajin, M.; Itoh, A.

    1994-10-01

    The uranium silicide U3Si2 has a congruent melting point of 1665 C and possesses higher uranium density (11.3 g U/cc) and higher thermal conductivity than the uranium dioxide currently used in light water reactors. U3Si2 is in use as a research reactor fuel (US Nuclear Regulatory Commission, NUREG-1313, July, 1988), representing a potentiality for power reactor fuel. A first attempt is made in this study to predict the chemical state of the solid fission-product elements comprising zirconium, molybdenum, rare earth elements, alkaline earth metals and elements of the platinum group. Ternary phase equilibria in the U-Mo-Si and U-Ru-Si systems are also investigated to supplement the fission product chemistry in U3Si2.

  12. Separation of the rare-earth fission product poisons from spent nuclear fuel

    SciTech Connect

    Christian, Jerry D.; Sterbentz, James W.

    2016-08-30

    A method for the separation of the rare-earth fission product poisons comprising providing a spent nuclear fuel. The spent nuclear fuel comprises UO.sub.2 and rare-earth oxides, preferably Sm, Gd, Nd, Eu oxides, with other elements depending on the fuel composition. Preferably, the provided nuclear fuel is a powder, preferably formed by crushing the nuclear fuel or using one or more oxidation-reduction cycles. A compound comprising Th or Zr, preferably metal, is provided. The provided nuclear fuel is mixed with the Th or Zr, thereby creating a mixture. The mixture is then heated to a temperature sufficient to reduce the UO.sub.2 in the nuclear fuel, preferably to at least to 850.degree. C. for Th and up to 600.degree. C. for Zr. Rare-earth metals are then extracted to form the heated mixture thereby producing a treated nuclear fuel. The treated nuclear fuel comprises the provided nuclear fuel having a significant reduction in rare-earths.

  13. Fission product release during a LOCA in VVER-440/213-type reactor

    SciTech Connect

    Sdouz, G. )

    1991-01-01

    In 1988, Austria initiated a research program to investigate the source term behavior of VVER-type reactors. Mainly, there are three design categories for VVER-type reactors. The first standardized 440-MW(electric) nuclear power plant was designated as VVER-440/MW(electric) nuclear power plant was designated as VVER-440/230. A somewhat more advanced model was designated as model V213. These reactors have six loops, isolation valves on each loop, horizontal steam generators, and hexagonal fuel assemblies. To prevent the release of fission products, the concept of local area compartmentalization is applied. The main difference between the two models is the existence of an emergency core cooling system (ECCS) and a bubbler-condenser tower in the newer model. In the 1970s, a 1000-MW(electric) reactor was designed and designated as VVER-1000. This unit has four loops housed in a containment-type structure with spray-type steam suppression. The Austrian program started with source term calculations for the VVEr-1000-type reactor. A TMLB{prime} and a S{sub 1}B accident sequence were calculated using the Source Term Code Package (STCP). In 1990, the source term analyses were extended to both models of the VVER-440-type reactors. In this paper, the results of the thermohydraulic part of the calculation for the VVER-440/213 reactor are presented.

  14. EXTRACTION METHOD FOR SEPARATING URANIUM, PLUTONIUM, AND FISSION PRODUCTS FROM COMPOSITIONS CONTAINING SAME

    DOEpatents

    Seaborg, G.T.

    1957-10-29

    Methods for separating plutonium from the fission products present in masses of neutron irradiated uranium are reported. The neutron irradiated uranium is first dissolved in an aqueous solution of nitric acid. The plutonium in this solution is present as plutonous nitrate. The aqueous solution is then agitated with an organic solvent, which is not miscible with water, such as diethyl ether. The ether extracts 90% of the uraryl nitrate leaving, substantially all of the plutonium in the aqueous phase. The aqueous solution of plutonous nitrate is then oxidized to the hexavalent state, and agitated with diethyl ether again. In the ether phase there is then obtained 90% of plutonium as a solution of plutonyl nitrate. The ether solution of plutonyl nitrate is then agitated with water containing a reducing agent such as sulfur dioxide, and the plutonium dissolves in the water and is reduced to the plutonous state. The uranyl nitrate remains in the ether. The plutonous nitrate in the water may be recovered by precipitation.

  15. Gas emission from the UO2 samples, containing fission products and burnable absorber

    NASA Astrophysics Data System (ADS)

    Kopytin, V. P.; Baranov, V. G.; Burlakova, M. A.; Tenishev, A. V.; Kuzmin, R. S.; Pokrovskiy, S. A.; Mikhalchik, V. V.

    2016-04-01

    The process gas released from the fuel pellets of uranium fuel during fuel burn-up reduces the thermal conductivity of the rod-shell gap, enhances hydrogen embrittlement of the cladding material, causes it's carbonization, as well as transport processes in the fuel. In this study a technique of investigating the thermal desorption of gases from the UO2 fuel material were perfected in the temperature range 300-2000 K for uniform sample heating rate of 15 K/min in vacuum. The characteristic kinetic dependences are acquired for the gas emission from UO2 samples, containing simulators of fission products (SFP) and the burnable neutron absorber (BNA). Depending on the amount of SFP and BNA contained in the sample thermal desorption gas spectra (TDGS) vary. The composition of emitted gas varies, as well as the number of peaks in the TDGS and the peaks shift to higher temperatures. This indicates that introduction of SFPs and BNA alters the sample material structure and cause the creation of so- called traps which have different bonding energies to the gases. The traps can be a grid of dislocations, voids, and contained in the UO2 matrix SFP and BNA. Similar processes will occur in the fuel pellets in the real conditions of the Nuclear Power Plant as well.

  16. DFT study of the hexagonal high-entropy alloy fission product system

    NASA Astrophysics Data System (ADS)

    King, D. J. M.; Burr, P. A.; Obbard, E. G.; Middleburgh, S. C.

    2017-05-01

    The metallic phase fission product containing Mo-Pd-Rh-Ru-Tc can be described as a hexagonal high-entropy alloy (HEA) and is thus investigated using atomic scale simulation techniques relevant to HEAs. Contrary to previous assumptions, the removal of Tc from the system to form the Mo-Pd-Rh-Ru analog is predicted to reduce the stability of the solid solution to the point that σ-Mo5Ru3 may precipitate out at typical fuel operating temperatures. The drive for segregation is attributed to the increased stability of the solid solution with the ejection of Mo and Ru. When Tc is included in the system, a single phase hexagonal solid solution is expected to form for a wider range of compositions. Furthermore, when cooled below 700 °C, this single phase solid solution is predicted to transition to a partially ordered structure. Future studies using the Tc-absent analogue will need to take these structural and chemical deliberations into consideration.

  17. Hot beta particles in the lung: Results from dogs exposed to fission product radionuclides

    SciTech Connect

    Hahn, F.F.; Griffith, W.C.; Hobbs, C.H.

    1995-12-01

    The Chernobyl nuclear reactor accident resulted in the release of uranium dioxide fuel and fission product radionuclides into the environment with the fallout of respirable, highly radioactive particles that have been termed {open_quotes}hot beta particles.{close_quotes} There is concern that these hot beta particles (containing an average of 150-20,000 Bq/particle), when inhaled and deposited in the lung, may present an extraordinary hazard for the induction of lung cancer. We reviewed data from a group of studies in dogs exposed to different quantities of beta-emitting radionuclides with varied physical half-lives to determine if those that inhaled hot beta particles were at unusual risk for lung cancer. This analysis indicates that the average dose to the lung is adequate to predict biologic effects of lung cancer for inhaled beta-emitting radionuclides in the range of 5-50 Gy to the lung and with particle activities in the range of 0.10-50 Bq/particle.

  18. Investigation on high temperature vapor pressure of UO 2 containing simulated fission-product elements

    NASA Astrophysics Data System (ADS)

    Yano, T.; Ohtsubo, A.; Ishii, T.

    1984-06-01

    During the hypothetical core disruptive accident (HCDA) of a fast breeder reactor (FBR), the temperature of the fuel would rise above 3000 K. The experimental data concerning the saturated fuel vapor pressure are necessary for the analysis of the HCDA. In this study, the UO 2 containing Cs, Ba, Ag, or Sn was used to simulate the irradiated fuel in the FBR. The saturated vapor pressure of pure UO 2 and UO 2 containing Cs, Ba, Ag, or Sn at 3000 to 5000 K was measured dynamically with a pulse laser and a torsion pendulum. The surface of a specimen on the pendulum was heated to eject vapor by the injection of a giant pulse ruby laser beam. The pressure of the ejected vapor was measured by both the maximum rotation angle of the pendulum and the duration of vapor ejection. The saturated vapor pressure was theoretically calculated by using the ejected vapor pressure. The surface temperature of the specimen was estimated from the irradiated energy density measured with a laser energy meter. The saturated vapor pressure of UO 2 at 3640 to 5880 K measured in this study was near the extrapolated value of Ackermann's low temperature data. The vapor pressure of UO 2 containing Cs, Ba, Ag or Sn was higher than that of UO 2. The saturated vapor pressure of UO 2 and a solid fission products system was calculated by using these experimental data.

  19. Electrochemical separation of actinides and fission products in molten salt electrolyte

    SciTech Connect

    Gay, R.L.; Grantham, L.F.; Fusselman, S.P.

    1995-10-01

    Molten salt electrochemical separation may be applied to accelerator-based conversion (ABC) and transmutation systems by dissolving the fluoride transport salt in LiCl-KCl eutectic solvent. The resulting fluoride-chloride mixture will contain small concentrations of fission product rare earths (La, Nd, Gd, Pr, Ce, Eu, Sm, and Y) and actinides (U, Np, Pu, Am, and Cm). The Gibbs free energies of formation of the metal chlorides are grouped advantageously such that the actinides can be deposited on a solid cathode with the majority of the rare earths remaining in the electrolyte. Thus, the actinides are recycled for further transmutation. Rockwell and its partners have measured the thermodynamic properties of the metal chlorides of interest (rare earths and actinides) and demonstrated separation of actinides from rare earths in laboratory studies. A model is being developed to predict the performance of a commercial electrochemical cell for separations starting with PUREX compositions. This model predicts excellent separation of plutonium and other actinides from the rare earths in metal-salt systems.

  20. Approach for validating actinide and fission product compositions for burnup credit criticality safety analyses

    DOE PAGES

    Radulescu, Georgeta; Gauld, Ian C.; Ilas, Germina; ...

    2014-11-01

    This paper describes a depletion code validation approach for criticality safety analysis using burnup credit for actinide and fission product nuclides in spent nuclear fuel (SNF) compositions. The technical basis for determining the uncertainties in the calculated nuclide concentrations is comparison of calculations to available measurements obtained from destructive radiochemical assay of SNF samples. Probability distributions developed for the uncertainties in the calculated nuclide concentrations were applied to the SNF compositions of a criticality safety analysis model by the use of a Monte Carlo uncertainty sampling method to determine bias and bias uncertainty in effective neutron multiplication factor. Application ofmore » the Monte Carlo uncertainty sampling approach is demonstrated for representative criticality safety analysis models of pressurized water reactor spent fuel pool storage racks and transportation packages using burnup-dependent nuclide concentrations calculated with SCALE 6.1 and the ENDF/B-VII nuclear data. Furthermore, the validation approach and results support a recent revision of the U.S. Nuclear Regulatory Commission Interim Staff Guidance 8.« less

  1. Waste form evaluation for RECl3 and REOx fission products separated from used electrochemical salt

    DOE PAGES

    Riley, Brian J.; Pierce, David A.; Crum, Jarrod V.; ...

    2017-09-22

    The work presented here is based off the concept that the rare earth chloride (RECl3) fission products within the used electrorefiner (ER) salt can be selectively removed as RECl3 (not yet demonstrated) or precipitated out as a mixture of REOCl and REOx through oxygen sparging (has been demonstrated). This paper presents data showing the feasibility of immobilizing a mixture of RECl3s at 10 mass% into a 78%TeO2-22%PbO glass while also showing that this same mixture of RECl3s can be oxidized to REOCl at 300 °C and then to REOx by 1200 °C, evolving Cl2(g). When the REOx mixture is heatedmore » at temperatures >1200 °C, the ratios of REOxs change. The mixture of REOx was then immobilized in a lanthanide borosilicate (LABS) glass at a high loading of 60 mass%. Both the 78%TeO2-22%PbO glass and LABS glass systems show good chemical durability. In conclusion, the advantages and disadvantages of tellurite and LABS glasses are compared.« less

  2. A scoping study of fission product transport from failed fuel during N Reactor postulated accidents

    SciTech Connect

    Hagrman, D.L.

    1988-01-01

    This report presents a scoping study of cesium, iodine, and tellurium behavior during a cold leg manifold break in the N Reactor. More detail about fission product behavior than has previously been available is provided and key parameters that control this behavior are identified. The LACE LA1 test and evidence from the Power Burst Facility Severe Fuel Damage tests are used to test the key model applied to determine aerosol behavior. Recommendations for future analysis are also provided. The primary result is that most of the cesium, iodine, and tellurium remains in the molten uranium fuel. Only 0.0035 of the total inventory is calculated to be released. Condensation of the most of the species of cesium and iodine that are released is calculated, with 0.998 of the released cesium and iodine condensing in the spacers and upstream end of the connector tubes. Most of the tellurium that is released condenses, but the chemical reaction of tellurium vapor with surfaces is also a major factor in the behavior of this element.

  3. High-Resolution Compton-Suppressed CZT Detector for Fission Products Identification

    SciTech Connect

    R. Aryaeinejd; J. K. Hartwell; Wade W. Scates

    2004-10-01

    Room temperature semiconductor CdZnTe (CZT) detectors are currently limited to total detector volumes of 1-2 cm3, which is dictated by the poor charge transport characteristics. Because of this size limitation one of the problems in accurately determining isotope identification is the enormous background from the Compton scattering events. Eliminating this background will not only increase the sensitivity and accuracy of measurements but also help us to resolve peaks buried under the background and peaks in close vicinity of others. We are currently developing a fission products detection system based on the Compton-suppressed CZT detector. In this application, the detection system is required to operate in high radiation fields. Therefore, a small 10x10x5 mm3 CZT detector is placed inside the center of a well-shielded 3" in diameter by 3" long Nal detector. So far we have been able to successfully reduce the Compton background by a factor of 5.4 for a 137Cs spectrum. This reduction of background will definitely enhance the quality of the gamma-ray spectrum in the information-rich energy range below 1 MeV, which consequently increases the detection sensitivity. In this work, we will discuss the performance of this detection system as well as its applications.

  4. Radiometric evaluation of diglycolamide resins for the chromatographic separation of actinium from fission product lanthanides

    DOE PAGES

    Radchenko, Valery; Mastren, Tara; Meyer, Catherine A. L.; ...

    2017-07-20

    Actinium-225 is a potential Targeted Alpha Therapy (TAT) isotope. It can be generated with high energy (≥ 100 MeV) proton irradiation of thorium targets. The main challenge in the chemical recovery of 225Ac lies in the separation from thorium and many fission by-products most importantly radiolanthanides. We recently developed a separation strategy based on a combination of cation exchange and extraction chromatography to isolate and purify 225Ac. In this study, actinium and lanthanide equilibrium distribution coefficients and column elution behavior for both TODGA (N,N,N',N'-tetra-n-octyldiglycolamide) and TEHDGA (N,N,N',N'-tetrakis-2-ethylhexyldiglycolamide) were determined. Density functional theory (DFT) calculations were performed and were in agreementmore » with experimental observations providing the foundation for understanding of the selectivity for Ac and lanthanides on different DGA (diglycolamide) based resins. The results of Gibbs energy (ΔGaq) calculations confirm significantly higher selectivity of DGA based resins for LnIII over AcIII in the presence of nitrate. As a result, DFT calculations and experimental results reveal that Ac chemistry cannot be predicted from lanthanide behavior under comparable circumstances.« less

  5. Disposal of type-II long-lived fission products into outer space

    SciTech Connect

    Takahashi, Hiroshi; Chen, Xinyi

    1996-12-31

    The authors propose an alternative approach to dispose of long-lived fission products (LLFPs) of type-II, such as {sup 79}Se, {sup 99}Tc, {sup 107}Pd, {sup 126}Sn, {sup 129}I, {sup 135}Cs, and long-lived radioactive {sup 93}Zr into outer solar space. An escape velocity from the solar system of 42 km/s will be provided from either a parking orbit or the moon`s surface using an electrostatic accelerator and by neutralizing the charged accelerated LLFPs ions. LLFP ions must be neutralized to avoid their being trapped in earth and solar magnetic fields; almost 100% neutralization can be achieved by recirculating the non-neutralized ions through a magnetic field in the neutralizing device. This mode of disposition requires 2.2 kW power to eject most of the LLFPs generated by one LWR. This process is much smaller than a medium-energy proton beam power, a few tens of MW, which would be necessary to transmute these LLFPs using spallation neutrons created by protons. Due to their low radioactivity composed of mainly beta decay and low-energy gamma-rays, the shielding needed is not excessive and can be easily accommodated.

  6. Fast-neutron interaction with the fission product {sup 103}Rh

    SciTech Connect

    Smith, A.B. |; Guenther, P.T.

    1993-09-01

    Neutron total and differential elastic- and inelastic-scattering cross sections of {sup 103}Rh are measured from {approximately} 0.7 to 4.5 MeV (totals) and from {approximately} 1.5 to 10 MeV (scattering) with sufficient detail to define the energy-averaged behavior of the neutron processes. Neutrons corresponding to excitations of groups of levels at 334 {plus_minus} 13, 536 {plus_minus} 10, 648 {plus_minus} 25, 796 {plus_minus} 20, 864 {plus_minus} 22, 1120 {plus_minus} 22, 1279 {plus_minus} 60, 1481 {plus_minus} 27 and 1683 {plus_minus} 39 keV were observed. Additional groups at 1840 {plus_minus} 79 and 1991 {plus_minus} 71 key were tentatively identified. Assuming the target is a collective nucleus reasonably approximated by a simple one-phonon vibrator, spherical-optical, dispersive-optical, and coupled-channels models were developed from the data base with attention to the parameterization of the large inelastic-scattering cross sections. The physical properties of these models are compared with theoretical predictions and the systematics of similar model parameterizations in this mass region. In particular, it is shown that the inelastic-scattering cross section of the {sup 103}Rh fission product is large at the relatively low energies of applied interest.

  7. A potential photo-transmutation of fission products triggered by Compton backscattering photons

    NASA Astrophysics Data System (ADS)

    Chen, J. G.; Xu, W.; Wang, H. W.; Guo, W.; Ma, Y. G.; Cai, X. Z.; Lu, G. C.; Xu, Y.; Pan, Q. Y.; Fan, G. T.; Shen, W. Q.

    2009-02-01

    We investigated the transmutation of some fission product nuclides I129, Cs135, Sn126, Zr93, Pd107, Cs137 and Sr90, induced by the Compton backscattering (CBS) photons generated from the future Shanghai Laser Electron Gamma Source (SLEGS) facility. The evaluated photo-transmutation rates for I129, Cs135, Sn126, Zr93, Pd107, Cs137 and Sr90 can achieve 2. 5×106, 1.3×106, 4.8×106, 2.7×106, 9.4×106, 1.3×106 and 1.6×106 per second, respectively, improving 4-5 orders of magnitude compared with those via the bremsstrahlung photons by a 1020 W/cm2 laser. The maximum transmutation coupling efficiencies of the CBS photons were estimated to be 1.36% for I129, 1.70% for Cs135, 2.02% for Sn126, 1.03% for Zr90, 1.52% for Pd107, 1.62% for Cs137 and 1.72% for Sr90, which are 2-6 times as those via the bremsstrahlung method by the 1020 W/cm2 laser. Moreover, we presented a possible experimental method for the future SLEGS facility to check the estimated results.

  8. Radiometric evaluation of diglycolamide resins for the chromatographic separation of actinium from fission product lanthanides.

    PubMed

    Radchenko, Valery; Mastren, Tara; Meyer, Catherine A L; Ivanov, Alexander S; Bryantsev, Vyacheslav S; Copping, Roy; Denton, David; Engle, Jonathan W; Griswold, Justin R; Murphy, Karen; Wilson, Justin J; Owens, Allison; Wyant, Lance; Birnbaum, Eva R; Fitzsimmons, Jonathan; Medvedev, Dmitri; Cutler, Cathy S; Mausner, Leonard F; Nortier, Meiring F; John, Kevin D; Mirzadeh, Saed; Fassbender, Michael E

    2017-12-01

    Actinium-225 is a potential Targeted Alpha Therapy (TAT) isotope. It can be generated with high energy (≥ 100MeV) proton irradiation of thorium targets. The main challenge in the chemical recovery of (225)Ac lies in the separation from thorium and many fission by-products most importantly radiolanthanides. We recently developed a separation strategy based on a combination of cation exchange and extraction chromatography to isolate and purify (225)Ac. In this study, actinium and lanthanide equilibrium distribution coefficients and column elution behavior for both TODGA (N,N,N',N'-tetra-n-octyldiglycolamide) and TEHDGA (N,N,N',N'-tetrakis-2-ethylhexyldiglycolamide) were determined. Density functional theory (DFT) calculations were performed and were in agreement with experimental observations providing the foundation for understanding of the selectivity for Ac and lanthanides on different DGA (diglycolamide) based resins. The results of Gibbs energy (ΔGaq) calculations confirm significantly higher selectivity of DGA based resins for Ln(III) over Ac(III) in the presence of nitrate. DFT calculations and experimental results reveal that Ac chemistry cannot be predicted from lanthanide behavior under comparable circumstances. Copyright © 2017 Elsevier B.V. All rights reserved.

  9. Disposal of long-lived fission products into the outer solar system

    SciTech Connect

    Takahashi, Hiroshi; Chen Xinyi; Yu An

    2002-07-01

    We propose approach to dispose of Long-Lived Fission Products (LLFPs) of type II such as {sup 99}Tc and {sup 129}I into outer solar space by providing an escape velocity from the solar system of 42 km/sec from a parking orbit or the moon's surface using a electrostatic accelerator and neutralizing the charged ions. LLFPs disposed uniformly in outer solar space pose no hazard as do LLFPs packages in Earth orbit, and have no effects on astronomical observations. This mode of disposition requires energy in the order of 1 keV for each nucleus, which is far smaller than the propulsion energy needed for launching a LLFPs package by rocket. Further, the power required of an accelerator ejecting most of the LLFPs generated by one LWR is 2.2 kW, which is much smaller than a medium-energy proton accelerator, a few tens of MW, which would be necessary to transmute these LLFPs using spallation neutrons created by protons. Ion thrusters, which has been developed for maneuvering rocket, might be used for disposition of LLFP instead of the a static accelerator, its usability is discussed. (authors)

  10. Approach for validating actinide and fission product compositions for burnup credit criticality safety analyses

    SciTech Connect

    Radulescu, Georgeta; Gauld, Ian C.; Ilas, Germina; Wagner, John C.

    2014-11-01

    This paper describes a depletion code validation approach for criticality safety analysis using burnup credit for actinide and fission product nuclides in spent nuclear fuel (SNF) compositions. The technical basis for determining the uncertainties in the calculated nuclide concentrations is comparison of calculations to available measurements obtained from destructive radiochemical assay of SNF samples. Probability distributions developed for the uncertainties in the calculated nuclide concentrations were applied to the SNF compositions of a criticality safety analysis model by the use of a Monte Carlo uncertainty sampling method to determine bias and bias uncertainty in effective neutron multiplication factor. Application of the Monte Carlo uncertainty sampling approach is demonstrated for representative criticality safety analysis models of pressurized water reactor spent fuel pool storage racks and transportation packages using burnup-dependent nuclide concentrations calculated with SCALE 6.1 and the ENDF/B-VII nuclear data. Furthermore, the validation approach and results support a recent revision of the U.S. Nuclear Regulatory Commission Interim Staff Guidance 8.

  11. Lanthanide fission product separation from the transuranics in the integral fast reactor fuel cycle demonstration

    SciTech Connect

    Goff, K.M.; Mariani, R.D.; Benedict, R.W.; Ackerman, J.P.

    1993-12-31

    The Integral Fast Reactor (IFR) is an innovative reactor concept being developed by Argonne National Laboratory. This reactor uses liquid-metal cooling and metallic fuel. Its spent fuel will be reprocessed using a pyrochemical method employing molten salts and liquid metals in an electrofining operation. The lanthanide fission products are a concern during reprocessing because of heating and fuel performance issues, so they must be removed periodically from the system to lessen their impact. The actinides must first be removed form the system before the lanthanides are removed as a waste stream. This operation requires a relatively good lanthanide-actinide separation to minimize both the amount of transuranic material lost in the waste stream and the amount of lanthanides collected when the actinides are first removed. A computer code, PYRO, that models these operations using thermodynamic and empirical data was developed at Argonne and has been used to model the removal of the lanthanides from the electrorefiner after a normal operating campaign. Data from this model are presented. The results demonstrate that greater that 75% of the lanthanides can be separated from the actinides at the end of the first fuel reprocessing campaign using only the electrorefiner vessel.

  12. Direct irradiation of long-lived fission products in an ATW system

    SciTech Connect

    Carter, T.F.; Henderson, D.; Sailor, W.C.

    1995-10-01

    The feasibility of directly irradiating five long-lived fission products (LLFPs: {sup 79}Se, {sup 93}Zr, {sup 107}Pd, {sup 126}Sn, and {sup 135}Cs, each with a half-life greater than 10,000 years), by incorporating them into the target of an Accelerator Transmutation of Waste (ATW) system is discussed. The important parameters used to judge the feasibility of a direct irradiation system were the target`s neutron spallation yield (given in neutrons produced per incident proton), and the removal rate of the LLFP, with the baseline incineration rate set at two light water reactors (LWRs) worth of the LLFP waste per year. A target was constructed which consisted of a LLFP cylindrical {open_quotes}plug{close_quotes} inserted into the top (where the proton beam strikes) of a 30 cm radius, 100 cm length lead target. {sup 126}Sn and {sup 79}Se were each found to have high enough removal rates to support two LWR`s production of the LLFP per year of ATW operation. For the baseline plug geometry (5 cm radius, 30 cm length) containing {sup 126}Sn, 3.5 LWRs could be supported per year (at 75% beam availability). Furthermore, the addition of a {sup 126}Sn plus had a slightly positive effect on the target`s neutron yield. The neutron production was 36.83 {plus_minus}.0039 neutrons per proton with a pure lead target having a yield of 36.29 {plus_minus}.0038. It was also found that a plug composed of a tin-selenide compound (SnSe) had high enough removal rates to burn two or more reactor years of both LLFPs simultaneously.

  13. Fission-Product Separation Based on Room-Temperature Ionic Liquids (OR08SP24-16)

    SciTech Connect

    Luo, Huimin; Bonnesen, Peter V.; Rogers, Robin D.; Dai, Sheng; Buchanan, A. C. III; Hussey, Charles L.

    2002-06-15

    The objectives of this project are (a) to synthesize new ionic liquids tailored for the extractive separation of Cs + and Sr 2+; (b) to select optimum macrocyclic extractants through studies of complexation of fission products with macrocyclic extractants and transport in new extraction systems based on ionic liquids; (c) to develop efficient processes to recycle ionic liquids and crown ethers; and (d) to investigate chemical stabilities of ionic liquids under strong acid, strong base, and high-level-radiation conditions.

  14. Deep Atomic Binding (DAB) Approach in Interpretation of Fission Products Behavior in Human Body, and Health Consequences

    SciTech Connect

    Ajlouni, Abdul-Wali M.S.

    2006-07-01

    According to models used to predict health effects of fission products enter the human body, a large number of fatalities, malignancies, thyroid cancer, born (genetic) defects,...etc.. But the actual data after Chernobyl and TMI accidents, and nuclear detonations in USA and Marshal Islands, were not consistent with these models. According to DAB, these data could be interpreted, and conflicts between former models predictions and actual field data explained. (author)

  15. Aqueous Biphasic Systems Based on Salting-Out Polyethylene Glycol or Ionic Solutions: Strategies for Actinide or Fission Product Separations

    SciTech Connect

    Rogers, Robin D.; Gutowski, Keith E.; Griffin, Scott T.; Holbrey, John D.

    2004-03-29

    Aqueous biphasic systems can be formed by salting-out (with kosmotropic, waterstructuring salts) water soluble polymers (e.g., polyethylene glycol) or aqueous solutions of a wide range of hydrophilic ionic liquids based on imidazolium, pyridinium, phosphonium and ammonium cations. The use of these novel liquid/liquid biphases for separation of actinides or other fission products associated with nuclear wastes (e.g., pertechnetate salts) has been demonstrated and will be described in this presentation.

  16. Payload dose rate from direct beam radiation and exhaust gas fission products. [for nuclear engine for rocket vehicles

    NASA Technical Reports Server (NTRS)

    Capo, M. A.; Mickle, R.

    1975-01-01

    A study was made to determine the dose rate at the payload position in the NERVA System (1) due to direct beam radiation and (2) due to the possible effect of fission products contained in the exhaust gases for various amounts of hydrogen propellant in the tank. Results indicate that the gamma radiation is more significant than the neutron flux. Under different assumptions the gamma contribution from the exhaust gases was 10 to 25 percent of total gamma flux.

  17. Licensing topical report: the measurement and modelling of time-dependent fission product release from failed HTGR fuel particles under accident conditions

    SciTech Connect

    Myers, B.F.; Morrissey, R.E.

    1980-04-01

    The release of fission products from failed fuel particles was measured under simulated accident (core heatup) conditions. A generic model and specific model parameters that describe delayed fission product release from the kernels of failed HTGR fuel particles were developed from the experimental results. The release of fission products was measured from laser-failed BISO ThO/sub 2/ and highly enriched (HEU) TRISO UC/sub 2/ particles that had been irradiated to a range of kernel burnups. The burnups were 0.25, 1.4, and 15.7% FIMA for ThO/sub 2/ particles and 23.5 and 74% FIMA for UC/sub 2/ particles. The fission products measured were nuclides of xenon, iodine, krypton, tellurium, and cesium.

  18. A generalized method for characterization of 235U and 239Pu content using short-lived fission product gamma spectroscopy

    DOE PAGES

    Knowles, Justin R.; Skutnik, Steven E.; Glasgow, David C.; ...

    2016-06-23

    Rapid non-destructive assay methods for trace fissile material analysis are needed in both nuclear forensics and safeguards communities. To address these needs, research at the High Flux Isotope Reactor Neutron Activation Analysis laboratory has developed a generalized non-destructive assay method to characterize materials containing fissile isotopes. This method relies on gamma-ray emissions from short-lived fission products and capitalizes off of differences in fission product yields to identify fissile compositions of trace material samples. Although prior work has explored the use of short-lived fission product gamma-ray measurements, the proposed method is the first to provide a holistic characterization of isotopic identification,more » mass ratios, and absolute mass determination. Successful single fissile isotope mass recoveries of less than 6% error have been conducted on standards of 235U and 239Pu as low as 12 nanograms in less than 10 minutes. Additionally, mixtures of fissile isotope standards containing 235U and 239Pu have been characterized as low as 229 nanograms of fissile mass with less than 12% error. The generalizability of this method is illustrated by evaluating different fissile isotopes, mixtures of fissile isotopes, and two different irradiation positions in the reactor. Furthermore, it is anticipated that this method will be expanded to characterize additional fissile nuclides, utilize various irradiation sources, and account for increasingly complex sample matrices.« less

  19. Fission product retention in TRISCO coated UO sub 2 particle fuels subjected to HTR simulated core heating tests

    SciTech Connect

    Baldwin, C.A.; Kania, M.J.

    1990-11-01

    Results of the examination and analysis of 25,730 individual microspheres from spherical fuel elements HFR-K3/1 and HFR-K3/3 are reported. The parent spheres were irradiated in excess of end-of-life exposure and subsequently subjected to simulated core heating tests in a special high-temperature furnace at Forschungszentrum, Juelich, GmbH (KFA). Following the heating tests, the spheres were electrolytically deconsolidated to obtain unbonded fuel particles for Irradiated Microsphere Gamma Analyzer (IMGA) analysis. For sphere HFR-K3/1, which was heated for 500 h at 1600{degree}C, only four particles were identified as having released fission products. The remaining particles from the sphere showed no statistical evidence of fission product release. Scanning Electron Microscopy (SEM) examination showed that three of the defect particles had large sections of the TRISO coating missing, while the fourth appeared normal. For sphere HFR-K3/3, which was heated for 100 h at 1800{degree}C, the IMGA data revealed that fission product release (cesium) from individual particles was significant and that there was large particle-to-particle variation in retention capabilities. Individual particle release (cesium) averaged ten times the KFA-measured integral spherical fuel element release value. In addition, the bimodal distribution of the individual particle data indicated that two distinct modes of failure at fuel temperatures of 1800{degree}C and above may exist. 6 refs., 6 figs., 4 tabs.

  20. Energetics of gaseous and volatile fission products in molten U-10Zr alloy: A density functional theory study

    NASA Astrophysics Data System (ADS)

    Wang, Ning; Tian, Jie; Jiang, Tao; Yang, Yanqiu; Hu, Sheng; Peng, Shuming; Yan, Liuming

    2015-11-01

    Gaseous and volatile fission products have a number of adverse effects on the safety and efficiency of the U-10Zr alloy fuel. The theoretical calculations were applied to investigate the energetics related to the formation, nucleation, and degassing of gaseous and volatile fission products (Kr, Xe and I) in molten U-10Zr alloy. The molecular dynamics (MD) simulations were applied to generate equilibrium configurations. The density functional theory (DFT) calculations were used to build atomistic models including molten U-10Zr alloy as well as its fission products substituted systems. The vacancy formation in liquid U-10Zr alloy were studied using DFT calculations, with average Gibbs free formation energies at 8.266 and 6.333 eV for U- and Zr-vacancies, respectively. And the interaction energies were -1.911 eV, -2.390 eV, and -1.826 eV for the I-I, Xe-Xe, and Kr-Kr interaction in lattice when two of the adjacent uranium atoms were substituted by gaseous atoms. So it could be concluded that the interaction between I, Kr, and Xe in lattice is powerful than the interaction between these two atoms and the other lattice atoms in U-10Zr.

  1. A generalized method for characterization of 235U and 239Pu content using short-lived fission product gamma spectroscopy

    NASA Astrophysics Data System (ADS)

    Knowles, Justin; Skutnik, Steven; Glasgow, David; Kapsimalis, Roger

    2016-10-01

    Rapid nondestructive assay methods for trace fissile material analysis are needed in both nuclear forensics and safeguards communities. To address these needs, research at the Oak Ridge National Laboratory High Flux Isotope Reactor Neutron Activation Analysis facility has developed a generalized nondestructive assay method to characterize materials containing fissile isotopes. This method relies on gamma-ray emissions from short-lived fission products and makes use of differences in fission product yields to identify fissile compositions of trace material samples. Although prior work has explored the use of short-lived fission product gamma-ray measurements, the proposed method is the first to provide a complete characterization of isotopic identification, mass ratios, and absolute mass determination. Successful single fissile isotope mass recoveries of less than 6% recovery bias have been conducted on standards of 235U and 239Pu as low as 12 ng in less than 10 minutes. Additionally, mixtures of fissile isotope standards containing 235U and 239Pu have been characterized as low as 198 ng of fissile mass with less than 7% recovery bias. The generalizability of this method is illustrated by evaluating different fissile isotopes, mixtures of fissile isotopes, and two different irradiation positions in the reactor. It is anticipated that this method will be expanded to characterize additional fissile nuclides, utilize various irradiation facilities, and account for increasingly complex sample matrices.

  2. Atmospheric Processing Module for Mars Propellant Production

    NASA Technical Reports Server (NTRS)

    Muscatello, Anthony; Gibson, Tracy; Captain, James; Athman, Robert; Nugent, Matthew; Parks, Steven; Devor, Robert

    2013-01-01

    The multi-NASA center Mars Atmosphere and Regolith COllector/PrOcessor for Lander Operations (MARCO POLO) project was established to build and demonstrate a methane/oxygen propellant production system in a Mars analog environment. Work at the Kennedy Space Center (KSC) Applied Chemistry Laboratory is focused on the Atmospheric Processing Module (APM). The purpose of the APM is to freeze carbon dioxide from a simulated Martian atmosphere containing the minor components nitrogen, argon, carbon monoxide, and water vapor at Martian pressures (8 torr) by using dual cryocoolers with alternating cycles of freezing and sublimation. The resulting pressurized CO2 is fed to a methanation subsystem where it is catalytically combined with hydrogen in a Sabatier reactor supplied by the Johnson Space Center (JSC) to make methane and water vapor. We first used a simplified once-through setup and later employed a HiCO2 recycling system to improve process efficiency. This presentation and paper will cover (1) the design and selection of major hardware items, such as the cryocoolers, pumps, tanks, chillers, and membrane separators, (2) the determination of the optimal cold head design and flow rates needed to meet the collection requirement of 88 g CO2/hr for 14 hr, (3) the testing of the CO2 freezer subsystem, and (4) the integration and testing of the two subsystems to verify the desired production rate of 31.7 g CH4/hr and 71.3 g H20/hr along with verification of their purity. The resulting 2.22 kg of CH4/O2 propellant per 14 hr day (including O2 from electrolysis of water recovered from regolith, which also supplies the H2 for methanation) is of the scale needed for a Mars Sample Return mission. In addition, the significance of the project to NASA's new Mars exploration plans will be discussed.

  3. Atmospheric Processing Module for Mars Propellant Production

    NASA Technical Reports Server (NTRS)

    Muscatello, Anthony; Gibson, Tracy; Captain, James; Athman, Robert; Nugent, Matthew; Parks, Steven; Devor, Robert

    2013-01-01

    The multi-NASA center Mars Atmosphere and Regolith COllector/PrOcessor for Lander Operations (MARCO POLO) project was established to build and demonstrate a methane/oxygen propellant production system in a Mars analog environment. Work at the Kennedy Space Center (KSC) Applied Chemistry Laboratory is focused on the Atmospheric Processing Module (APM). The purpose of the APM is to freeze carbon dioxide from a simulated Martian atmosphere containing the minor components nitrogen, argon, carbon monoxide, and water vapor at Martian pressures (approx.8 torr) by using dual cryocoolers with alternating cycles of freezing and sublimation. The resulting pressurized CO2 is fed to a methanation subsystem where it is catalytically combined with hydrogen in a Sabatier reactor supplied by the Johnson Space Center (JSC) to make methane and water vapor. We first used a simplified once-through setup and later employed a HiCO2 recycling system to improve process efficiency. This presentation and paper will cover (1) the design and selection of major hardware items, such as the cryocoolers, pumps, tanks, chillers, and membrane separators, (2) the determination of the optimal cold head design and flow rates needed to meet the collection requirement of 88 g CO2/hr for 14 hr, (3) the testing of the CO2 freezer subsystem, and (4) the integration and testing of the two subsystems to verify the desired production rate of 31.7 g CH4/hr and 71.3 g H2O/hr along with verification of their purity. The resulting 2.22 kg of CH4/O2 propellant per 14 hr day (including O2 from electrolysis of water recovered from regolith, which also supplies the H2 for methanation) is of the scale needed for a Mars Sample Return mission. In addition, the significance of the project to NASA's new Mars exploration plans will be discussed.

  4. A physical description of fission product behavior fuels for advanced power reactors.

    SciTech Connect

    Kaganas, G.; Rest, J.; Nuclear Engineering Division; Florida International Univ.

    2007-10-18

    The Global Nuclear Energy Partnership (GNEP) is considering a list of reactors and nuclear fuels as part of its chartered initiative. Because many of the candidate materials have not been explored experimentally under the conditions of interest, and in order to economize on program costs, analytical support in the form of combined first principle and mechanistic modeling is highly desirable. The present work is a compilation of mechanistic models developed in order to describe the fission product behavior of irradiated nuclear fuel. The mechanistic nature of the model development allows for the possibility of describing a range of nuclear fuels under varying operating conditions. Key sources include the FASTGRASS code with an application to UO{sub 2} power reactor fuel and the Dispersion Analysis Research Tool (DART ) with an application to uranium-silicide and uranium-molybdenum research reactor fuel. Described behavior mechanisms are divided into subdivisions treating fundamental materials processes under normal operation as well as the effect of transient heating conditions on these processes. Model topics discussed include intra- and intergranular gas-atom and bubble diffusion, bubble nucleation and growth, gas-atom re-solution, fuel swelling and ?scion gas release. In addition, the effect of an evolving microstructure on these processes (e.g., irradiation-induced recrystallization) is considered. The uranium-alloy fuel, U-xPu-Zr, is investigated and behavior mechanisms are proposed for swelling in the {alpha}-, intermediate- and {gamma}-uranium zones of this fuel. The work reviews the FASTGRASS kinetic/mechanistic description of volatile ?scion products and, separately, the basis for the DART calculation of bubble behavior in amorphous fuels. Development areas and applications for physical nuclear fuel models are identified.

  5. Energy dependence of fission product yields from 235U, 238U, and 239Pu with monoenergetic neutrons between thermal and 14.8 MeV

    NASA Astrophysics Data System (ADS)

    Gooden, Matthew; Arnold, Charles; Bhike, Megha; Bredeweg, Todd; Fowler, Malcolm; Krishichayan; Tonchev, Anton; Tornow, Werner; Stoyer, Mark; Vieira, David; Wilhelmy, Jerry

    2017-09-01

    Under a joint collaboration between TUNL-LANL-LLNL, a set of absolute fission product yield measurements has been performed. The energy dependence of a number of cumulative fission product yields (FPY) have been measured using quasi-monoenergetic neutron beams for three actinide targets, 235U, 238U and 239Pu, between 0.5 and 14.8 MeV. The FPYs were measured by a combination of fission counting using specially designed dual-fission chambers and γ-ray counting. Each dual-fission chamber is a back-to-back ionization chamber encasing an activation target in the center with thin deposits of the same target isotope in each chamber. This method allows for the direct measurement of the total number of fissions in the activation target with no reference to the fission cross-section, thus reducing uncertainties. γ-ray counting of the activation target was performed on well-shielded HPGe detectors over a period of two months post irradiation to properly identify fission products. Reported are absolute cumulative fission product yields for incident neutron energies of 0.5, 1.37, 2.4, 3.6, 4.6, 5.5, 7.5, 8.9 and 14.8 MeV. Preliminary results from thermal irradiations at the MIT research reactor will also be presented and compared to present data and evaluations. This work was performed under the auspices of the U.S. Department of Energy by Los Alamos National Security, LLC under contract DE-AC52-06NA25396, Lawrence Livermore National Laboratory under contract DE-AC52-07NA27344 and by Duke University and Triangle Universities Nuclear Laboratory through NNSA Stewardship Science Academic Alliance grant No. DE-FG52-09NA29465, DE-FG52-09NA29448 and Office of Nuclear Physics Grant No. DE-FG02-97ER41033.

  6. In-pile release behavior of metallic fission products in graphite materials of an htgr fuel assembly

    NASA Astrophysics Data System (ADS)

    Hayashi, K.; Kobayashi, F.; Minato, K.; Ikawa, K.; Fukuda, K.

    1987-06-01

    Distribution of metallic fission products in the graphite sleeve and block of the fifth OGL-1 fuel assembly was measured by gamma spectrometry with lathe sectioning. Considerably large release fractions of long-lived fission products with smooth axial profiles were observed in the sleeve due to a large failure fraction of coated fuel particles accompanied with failed silicon carbide layers. Nevertheless, a key nuclide 110mAg, whose large release is suspected at increased burnups for low-enriched uranium fuels, was effectively retained within the graphite sleeve. The retention was also observed for 125Sb, 154Eu and 155Eu up to a burnup of 3.2% fission per initial metal atom, but was limited for 134Cs and 137Cs at high sleeve-temperatures above 900°C. In-pile diffusion coefficients in IG-110 graphite have been evaluated for Cs, Ag and Sb; those for Cs are in reasonable agreement with available in-pile data.

  7. Fission product release and microstructure changes of irradiated MOX fuel at high temperatures

    NASA Astrophysics Data System (ADS)

    Colle, J.-Y.; Hiernaut, J.-P.; Wiss, T.; Beneš, O.; Thiele, H.; Papaioannou, D.; Rondinella, V. V.; Sasahara, A.; Sonoda, T.; Konings, R. J. M.

    2013-11-01

    burnups correspond reasonably well with measurement of Walker et al. [11]. All those data are shown Fig. 2.Fragments of 2-8 mg were chosen for the experiments. Since these specimens are small compared to the drilled sample size and were taken randomly, the precise radial position could not be determined, in particular the specimens of sample type, A and B could be from close radial locations.Specimens from each drilled sample type were annealed up to complete vaporisation (˜2600 K) at a speed of about 10 K min-1 in a Knudsen effusion mass spectrometer (KEMS) described previously [13,14]. In addition to helium and to the FGs all the species present in the vapour between 83 and 300 a.m.u. were measured during the heating. Additionally, the 85Kr isotope was analysed in a cold trap by β and γ counting. The long-lived fission gas isotopes correspond to masses 131, 132, 134 and 136 for Xe and 83, 84, 85 and 86 for Kr. The absolute quantities of gas released from specimens of sample types A and B were also determined using the in-house built Q-GAMES (Quantitative gas measurement system), described in detail in [15].For each of the samples, fragments were also annealed and measured in the KEMS up to specific temperatures corresponding to different stages of the FGs or He release. These fragments were subsequently analysed by Scanning Electron Microscopy (SEM, Philips XL40) [16] in order to investigate the relationship between structural changes, burn-up, irradiation temperature and fission products release. SEM observations were also done on the samples before the KEMS experiments and the fracture surface appearance of the samples is shown in Fig. 3, revealing the presence of the high burnup structure (HBS) in the Pu-rich agglomerates.A summary of the 12 samples analysed by KEMS, SEM and Q-GAMES is given in Table 1. At 1300 K no clear change potentially related to gas release appears in the UM and PA. At 1450 K a beginning of grain boundaries opening can be observed as well as

  8. Nuclear Fission

    NASA Astrophysics Data System (ADS)

    Denschlag, J. O.

    This chapter first gives a survey on the history of the discovery of nuclear fission. It briefly presents the liquid-drop and shell models and their application to the fission process. The most important quantities accessible to experimental determination such as mass yields, nuclear charge distribution, prompt neutron emission, kinetic energy distribution, ternary fragment yields, angular distributions, and properties of fission isomers are presented as well as the instrumentation and techniques used for their measurement. The contribution concentrates on the fundamental aspects of nuclear fission. The practical aspects of nuclear fission are discussed in http://dx.doi.org/10.1007/978-1-4419-0720-2_57 of Vol. 6.

  9. Evaluation of Fission Product Critical Experiments and Associated Biases for Burnup Credit Validation

    SciTech Connect

    Mueller, Don; Rearden, Bradley T; Reed, Davis Allan

    2010-01-01

    One of the challenges associated with implementation of burnup credit is the validation of criticality calculations used in the safety evaluation; in particular the availability and use of applicable critical experiment data. The purpose of the validation is to quantify the relationship between reality and calculated results. Validation and determination of bias and bias uncertainty require the identification of sets of critical experiments that are similar to the criticality safety models. A principal challenge for crediting fission products (FP) in a burnup credit safety evaluation is the limited availability of relevant FP critical experiments for bias and bias uncertainty determination. This paper provides an evaluation of the available critical experiments that include FPs, along with bounding, burnup-dependent estimates of FP biases generated by combining energy dependent sensitivity data for a typical burnup credit application with the nuclear data uncertainty information distributed with SCALE 6. A method for determining separate bias and bias uncertainty values for individual FPs and illustrative results is presented. Finally, a FP bias calculation method based on data adjustment techniques and reactivity sensitivity coefficients calculated with the SCALE sensitivity/uncertainty tools and some typical results is presented. Using the methods described in this paper, the cross-section bias for a representative high-capacity spent fuel cask associated with the ENDF/B-VII nuclear data for 16 most important stable or near stable FPs is predicted to be no greater than 2% of the total worth of the 16 FPs, or less than 0.13 % k/k.

  10. NEUTRON CROSS SECTION EVALUATIONS OF FISSION PRODUCTS BELOW THE FAST ENERGY REGION

    SciTech Connect

    OH,S.Y.; CHANG,J.; MUGHABGHAB,S.

    2000-05-11

    Neutron cross section evaluations of the fission-product isotopes, {sup 95}Mo, {sup 99}Tc, {sup 101}Ru, {sup 103}Rh, {sup 105}Pd, {sup 109}Ag, {sup 131}Xe, {sup 133}Cs, {sup 141}Pr, {sup 141}Nd, {sup 147}Sm, {sup 149}Sm, {sup 150}Sm, {sup 151}Sm, {sup 152}Sm, {sup 153}Eu, {sup 155}Gd, and {sup 157}Gd were carried out below the fast neutron energy region within the framework of the BNL-KAERI international collaboration. In the thermal energy region, the energy dependence of the various cross-sections was calculated by applying the multi-level Breit-Wigner formalism. In particular, the strong energy dependence of the coherent scattering lengths of {sup 155}Gd and {sup 157}Gd were determined and were compared with recent calculations of Lynn and Seeger. In the resonance region, the recommended resonance parameters, reported in the BNL compilation, were updated by considering resonance parameter information published in the literature since 1981. The s-wave and, if available, p-wave reduced neutron widths were analyzed in terms of the Porter-Thomas distribution to determine the average level spacings and the neutron strength functions. Average radiative widths were also calculated from measured values of resolved energy resonances. The average resonance parameters determined in this study were compared with those in the BNL and other compilations, as well as the ENDF/B-VI, JEF-2.2, and JENDL-3.2 data libraries. The unresolved capture cross sections of these isotopes, computed with the determined average resonance parameters, were compared with measurements, as well as the ENDF/B-VI evaluations. To achieve agreement with the measurements, in a few cases minor adjustments in the average resonance parameters were made. Because of astrophysical interest, the Maxwellian capture cross sections of these nuclides at a neutron temperature of 30 keV were computed and were compared with other compilations and evaluations.

  11. Radioactive Fission Product Release from Defective Light Water Reactor Fuel Elements

    SciTech Connect

    Konyashov, Vadim V.; Krasnov, Alexander M.

    2002-04-15

    Results are provided of the experimental investigation of radioactive fission product (RFP) release, i.e., krypton, xenon, and iodine radionuclides from fuel elements with initial defects during long-term (3 to 5 yr) irradiation under low linear power (5 to 12 kW/m) and during special experiments in the VK-50 vessel-type boiling water reactor.The calculation model for the RFP release from the fuel-to-cladding gap of the defective fuel element into coolant was developed. It takes into account the convective transport in the fuel-to-cladding gap and RFP sorption on the internal cladding surface and is in good agreement with the available experimental data. An approximate analytical solution of the transport equation is given. The calculation dependencies of the RFP release coefficients on the main parameters such as defect size, fuel-to-cladding gap, temperature of the internal cladding surface, and radioactive decay constant were analyzed.It is shown that the change of the RFP release from the fuel elements with the initial defects during long-term irradiation is, mainly, caused by fuel swelling followed by reduction of the fuel-to-cladding gap and the fuel temperature. The calculation model for the RFP release from defective fuel elements applicable to light water reactors (LWRs) was developed. It takes into account the change of the defective fuel element parameters during long-term irradiation. The calculation error according to the program does not exceed 30% over all the linear power change range of the LWR fuel elements (from 5 to 26 kW/m)

  12. Neutrinos from charm production in the atmosphere

    SciTech Connect

    Enberg, Rikard

    2014-11-18

    Atmospheric neutrinos are produced in interactions of cosmic rays with Earth's atmosphere. At very high energy, the contribution from semi-leptonic decays of charmed hadrons, known as the prompt neutrino flux, dominates over the conventional flux from pion and kaon decays. This is due to the very short lifetime of the charmed hadrons, which therefore do not lose energy before they decay. The calculation of this process is difficult because the Bjorken-x at which the parton distribution functions are evaluated is very small. This is a region where QCD is not well understood, and large logarithms must be resummed. Available parton distribution functions are not known at such small x and extrapolations must be made. Theoretically, the fast rise of the structure functions for small x ultimately leads to parton saturation. This contribution describes the 'ERS' [1] calculation of the prompt neutrino flux, which includes parton saturation effects in the QCD production cross section of charm quarks. The ERS flux calculation is used by e.g. the IceCube collaboration as a standard benchmark background. We are now updating this calculation to take into account the recent LHC data on the charm cross section, as well as recent theoretical developments in QCD. Some of the issues involved in this calculation are described.

  13. Analyzing Losses: Transuranics into Waste and Fission Products into Recycled Fuel

    SciTech Connect

    Steven J. Piet; Nick R. Soelberg; Samuel E. Bays; Robert E. Cherry; Layne F. Pincock; Eric L. Shaber; Melissa C. Teague; Gregory M. Teske; Kurt G. Vedros; Candido Pereira; Denia Djokic

    2010-11-01

    All mass streams from separations and fuel fabrication are products that must meet criteria. Those headed for disposal must meet waste acceptance criteria (WAC) for the eventual disposal sites corresponding to their waste classification. Those headed for reuse must meet fuel or target impurity limits. A “loss” is any material that ends up where it is undesired. The various types of losses are linked in the sense that as the loss of transuranic (TRU) material into waste is reduced, often the loss or carryover of waste into TRU or uranium is increased. We have analyzed four separation options and two fuel fabrication options in a generic fuel cycle. The separation options are aqueous uranium extraction plus (UREX+1), electrochemical, Atomics International reduction oxidation separation (AIROX), and melt refining. UREX+1 and electrochemical are traditional, full separation techniques. AIROX and melt refining are taken as examples of limited separations, also known as minimum fuel treatment. The fuels are oxide and metal. To define a generic fuel cycle, a fuel recycling loop is fed from used light water reactor (LWR) uranium oxide fuel (UOX) at 51 MWth-day/kg-iHM burnup. The recycling loop uses a fast reactor with TRU conversion ratio (CR) of 0.50. Excess recovered uranium is put into storage. Only waste, not used fuel, is disposed – unless the impurities accumulate to a level so that it is impossible to make new fuel for the fast reactor. Impurities accumulate as dictated by separation removal and fission product generation. Our model approximates adjustment to fast reactor fuel stream blending of TRU and U products from incoming LWR UOX and recycling FR fuel to compensate for impurity accumulation by adjusting TRU:U ratios. Our mass flow model ignores postulated fuel impurity limits; we compare the calculated impurity values with those limits to identify elements of concern. AIROX and melt refining cannot be used to separate used LWR UOX-51 because they cannot

  14. Actinide Recovery Experiments with Bench-Scale Liquid Cadmium Cathode in Fission Product-Laden Molten Salt

    SciTech Connect

    S. X. Li; S. D. Herrmann; R. W. Benedict; K. M. Goff; M. F. Simpson

    2009-02-01

    This article summarizes the observations and analytical results from a series of bench- scale liquid cadmium cathode experiments that recovered transuranic elements together with uranium from a molten electrolyte laden with real fission products. Variable parameters such as the ratio of Pu3+/U3+ in the electrolyte, liquid cadmium cathode voltage, and feed materials were tested in the LCC experiments. Actinide recovery efficiency and Pu/U ratio in the liquid cadmium cathode product under variable conditions are reported in the article. Separation factors for actinides and rare earth elements in the salt/cadmium system are also presented.

  15. Solar Versus Fission Surface Power for Mars

    NASA Technical Reports Server (NTRS)

    Rucker, Michelle A.; Oleson, Steve; George, Pat; Landis, Geoffrey A.; Fincannon, James; Bogner, Amee; Jones, Robert E.; Turnbull, Elizabeth; McNatt, Jeremiah; Martini, Michael C.; Gyekenyesi, John Z.; Colozza, Anthony J.; Schmitz, Paul C.; Packard, Thomas W.

    2016-01-01

    A multi-discipline team of experts from the National Aeronautics and Space Administration (NASA) developed Mars surface power system point design solutions for two conceptual missions to Mars using In-situ resource utilization (ISRU). The primary goal of this study was to compare the relative merits of solar- versus fission-powered versions of each surface mission. First, the team compared three different solar-power options against a fission power system concept for a sub-scale, uncrewed demonstration mission. This “pathfinder” design utilized a 4.5 meter diameter lander. Its primary mission would be to demonstrate Mars entry, descent, and landing techniques. Once on the Martian surface, the lander’s ISRU payload would demonstrate liquid oxygen propellant production from atmospheric resources. For the purpose of this exercise, location was assumed to be at the Martian equator. The three solar concepts considered included a system that only operated during daylight hours (at roughly half the daily propellant production rate of a round-the-clock fission design), a battery-augmented system that operated through the night (matching the fission concept’s propellant production rate), and a system that operated only during daylight, but at a higher rate (again, matching the fission concept’s propellant production rate). Including 30% mass growth allowance, total payload masses for the three solar concepts ranged from 1,128 to 2,425 kg, versus the 2,751 kg fission power scheme. However, solar power masses increase as landing sites are selected further from the equator, making landing site selection a key driver in the final power system decision. The team also noted that detailed reliability analysis should be performed on daytime-only solar power schemes to assess potential issues with frequent ISRU system on/off cycling.

  16. Atmospheric Processing Module for Mars Propellant Production

    NASA Technical Reports Server (NTRS)

    Muscatello, A.; Devor, R.; Captain, J.

    2014-01-01

    The multi-NASA center Mars Atmosphere and Regolith COllector/PrOcessor for Lander Operations (MARCO POLO) project was established to build and demonstrate a methaneoxygen propellant production system in a Mars analog environment. Work at the Kennedy Space Center (KSC) Applied Chemistry Laboratory is focused on the Atmospheric Processing Module (APM). The purpose of the APM is to freeze carbon dioxide from a simulated Martian atmosphere containing the minor components nitrogen, argon, carbon monoxide, and water vapor at Martian pressures (approx. 8 torr) by using dual cryocoolers with alternating cycles of freezing and sublimation. The resulting pressurized CO(sub 2) is fed to a methanation subsystem where it is catalytically combined with hydrogen in a Sabatier reactor supplied by the Johnson Space Center (JSC) to make methane and water vapor. We first used a simplified once-through setup and later employed a H(sub 2)CO(sub 2) recycling system to improve process efficiency. This presentation and paper will cover (1) the design and selection of major hardware items, such as the cryocoolers, pumps, tanks, chillers, and membrane separators, (2) the determination of the optimal cold head design and flow rates needed to meet the collection requirement of 88 g CO(sub 2) hr for 14 hr, (3) the testing of the CO(sub 2) freezer subsystem, and (4) the integration and testing of the two subsystems to verify the desired production rate of 31.7 g CH(sub 4) hr and 71.3 g H(sub 2)O hr along with verification of their purity. The resulting 2.22 kg of CH(sub 2)O(sub 2) propellant per 14 hr day (including O(sub 2) from electrolysis of water recovered from regolith, which also supplies the H(sub 2) for methanation) is of the scale needed for a Mars Sample Return mission. In addition, the significance of the project to NASAs new Mars exploration plans will be discussed.

  17. Atmospheric Processing Module for Mars Propellant Production

    NASA Technical Reports Server (NTRS)

    Muscatello, Anthony C.

    2014-01-01

    The multi-NASA center Mars Atmosphere and Regolith COllectorPrOcessor for Lander Operations (MARCO POLO) project was established to build and demonstrate a methaneoxygen propellant production system in a Mars analog environment. Work at the Kennedy Space Center (KSC) Applied Chemistry Laboratory is focused on the Atmospheric Processing Module (APM). The purpose of the APM is to freeze carbon dioxide from a simulated Martian atmosphere containing the minor components nitrogen, argon, carbon monoxide, and water vapor at Martian pressures (8 torr) by using dual cryocoolers with alternating cycles of freezing and sublimation. The resulting pressurized CO(sub 2) is fed to a methanation subsystem where it is catalytically combined with hydrogen in a Sabatier reactor supplied by the Johnson Space Center (JSC) to make methane and water vapor. We first used a simplified once-through setup and later employed a H(sub 2)CO(sub 2) recycling system to improve process efficiency. This presentation and paper will cover (1) the design and selection of major hardware items, such as the cryocoolers, pumps, tanks, chillers, and membrane separators, (2) the determination of the optimal cold head design and flow rates needed to meet the collection requirement of 88 g CO(sub 2) hr for 14 hr, (3) the testing of the CO(sub 2) freezer subsystem, and (4) the integration and testing of the two subsystems to verify the desired production rate of 31.7 g CH(sub 4) hr and 71.3 g H(sub 2)O hr along with verification of their purity. The resulting 2.22 kg of CH(sub 2)O(sub 2) propellant per 14 hr day (including O(sub 2) from electrolysis of water recovered from regolith, which also supplies the H(sub 2) for methanation) is of the scale needed for a Mars Sample Return mission. In addition, the significance of the project to NASAs new Mars exploration plans will be discussed.

  18. Effects of radiation and fission product incorporation in a yttria-stabilized zirconia based inert matrix fuel

    NASA Astrophysics Data System (ADS)

    Zhu, Sha

    This work has investigated the irradiation and incorporation effects of fission products in a yttria-stabilized zirconia (YSZ) based inert matrix fuel (IMF). The concept of inert matrix fuel is based on a new strategy for disposition of plutonium generated from the reprocessing of commercial nuclear fuel and the dismantling of nuclear weapons, i.e. using uranium-free oxides to "burn" plutonium and other actinides (Np, Cm, and Am) in reactors. This approach allows direct disposal, without reprocessing, after once-through burn-up. YSZ and MgAl2O4-YSZ composites are among the potential ceramics for IMF due to their high chemical durability and radiation resistance. The research involved investigating the production, nature, and accumulation of irradiation-induced defects, the behavior of the fission products in the ceramics, the structural stability and amorphization resistance of the YSZ during implantation. Ion implantations were conducted with 200--400 keV Cs+, Sr+, I+, Xe+ and Ti+ up to fluences of 1 x 1017/cm 2 at both room temperature and temperatures of 600--700°C. Thermal annealing was subsequently completed after room temperature ion implantations. In situ and ex situ transmission electron microscopy (TEM), optical absorption spectroscopy, photo-luminescence spectroscopy, and electron paramagnetic resonance (EPR) spectroscopy were employed to characterize the irradiation induced defect evolution and analyze the defect structures. Various irradiation effects were observed and determined in the experiments, such as point defects (F type and V type color centers), defect clusters (dislocation loops), cavities (voids and bubbles), the crystalline-to-amorphous transition, and the phase transformation from fluorite to pyrochlore structure. The ion irradiation-induced amorphization mechanism, the retention ability of the fission products, and structural stability of YSZ are discussed in terms of ion incorporation effects, implanted ion radii, and the solubility

  19. Parallel computation safety analysis irradiation targets fission product molybdenum in neutronic aspect using the successive over-relaxation algorithm

    NASA Astrophysics Data System (ADS)

    Susmikanti, Mike; Dewayatna, Winter; Sulistyo, Yos

    2014-09-01

    One of the research activities in support of commercial radioisotope production program is a safety research on target FPM (Fission Product Molybdenum) irradiation. FPM targets form a tube made of stainless steel which contains nuclear-grade high-enrichment uranium. The FPM irradiation tube is intended to obtain fission products. Fission materials such as Mo99 used widely the form of kits in the medical world. The neutronics problem is solved using first-order perturbation theory derived from the diffusion equation for four groups. In contrast, Mo isotopes have longer half-lives, about 3 days (66 hours), so the delivery of radioisotopes to consumer centers and storage is possible though still limited. The production of this isotope potentially gives significant economic value. The criticality and flux in multigroup diffusion model was calculated for various irradiation positions and uranium contents. This model involves complex computation, with large and sparse matrix system. Several parallel algorithms have been developed for the sparse and large matrix solution. In this paper, a successive over-relaxation (SOR) algorithm was implemented for the calculation of reactivity coefficients which can be done in parallel. Previous works performed reactivity calculations serially with Gauss-Seidel iteratives. The parallel method can be used to solve multigroup diffusion equation system and calculate the criticality and reactivity coefficients. In this research a computer code was developed to exploit parallel processing to perform reactivity calculations which were to be used in safety analysis. The parallel processing in the multicore computer system allows the calculation to be performed more quickly. This code was applied for the safety limits calculation of irradiated FPM targets containing highly enriched uranium. The results of calculations neutron show that for uranium contents of 1.7676 g and 6.1866 g (× 106 cm-1) in a tube, their delta reactivities are the still

  20. Actinide, Activation Product and Fission Product Decay Data for Reactor-based Applications

    SciTech Connect

    Perry, R.J.; Dean, C.J.; Nichols, A.L.

    2014-06-15

    The UK Activation Product Decay Data Library was first released in September 1977 as UK-PADD1, to be followed by regular improvements on an almost yearly basis up to the assembly of UKPADD6.12 in March 2013. Similarly, the UK Heavy Element and Actinide Decay Data Library followed in December 1981 as UKHEDD1, with the implementation of various modifications leading to UKHEDD2.6, February 2008. Both the data content and evaluation procedures are defined, and the most recent evaluations are described in terms of specific radionuclides and the resulting consistency of their recommended decay-data files. New versions of the UKPADD and UKHEDD libraries are regularly submitted to the NEA Data Bank for possible inclusion in the JEFF library.

  1. Cement As a Waste Form for Nuclear Fission Products: The Case of 90Sr and Its Daughters [Cement As a Container for Nuclear Fission Products: The Case of 90Sr and Its Daughters

    SciTech Connect

    Dezerald, Lucile; Kohanoff, Jorge J.; Correa, Alfredo A.; Caro, Alfredo; Pellenq, Roland J. -M.; Ulm, Franz J.; Saul, Andres

    2015-10-29

    One of the main challenges faced by the nuclear industry is the long-term confinement of nuclear waste. Because it is inexpensive and easy to manufacture, cement is the material of choice to store large volumes of radioactive materials, in particular the low-level medium-lived fission products. It is therefore of utmost importance to assess the chemical and structural stability of cement containing radioactive species. Here, we use ab initio calculations based on density functional theory (DFT) to study the effects of 90Sr insertion and decay in C–S–H (calcium-silicate-hydrate) in order to test the ability of cement to trap and hold this radioactive fission product and to investigate the consequences of its β-decay on the cement paste structure. We show that 90Sr is stable when it substitutes the Ca2+ ions in C–S–H, and so is its daughter nucleus 90Y after β-decay. Interestingly, 90Zr, daughter of 90Y and final product in the decay sequence, is found to be unstable compared to the bulk phase of the element at zero K but stable when compared to the solvated ion in water. Furthermore, cement appears as a suitable waste form for 90Sr storage.

  2. Cement As a Waste Form for Nuclear Fission Products: The Case of 90Sr and Its Daughters [Cement As a Container for Nuclear Fission Products: The Case of 90Sr and Its Daughters

    DOE PAGES

    Dezerald, Lucile; Kohanoff, Jorge J.; Correa, Alfredo A.; ...

    2015-10-29

    One of the main challenges faced by the nuclear industry is the long-term confinement of nuclear waste. Because it is inexpensive and easy to manufacture, cement is the material of choice to store large volumes of radioactive materials, in particular the low-level medium-lived fission products. It is therefore of utmost importance to assess the chemical and structural stability of cement containing radioactive species. Here, we use ab initio calculations based on density functional theory (DFT) to study the effects of 90Sr insertion and decay in C–S–H (calcium-silicate-hydrate) in order to test the ability of cement to trap and hold thismore » radioactive fission product and to investigate the consequences of its β-decay on the cement paste structure. We show that 90Sr is stable when it substitutes the Ca2+ ions in C–S–H, and so is its daughter nucleus 90Y after β-decay. Interestingly, 90Zr, daughter of 90Y and final product in the decay sequence, is found to be unstable compared to the bulk phase of the element at zero K but stable when compared to the solvated ion in water. Furthermore, cement appears as a suitable waste form for 90Sr storage.« less

  3. Determination of gaseous fission product yields from 14 MeV neutron induced fission of 238U at the National Ignition Facility

    DOE PAGES

    Cassata, W. S.; Velsko, C. A.; Stoeffl, W.; ...

    2016-01-14

    We determined fission yields of xenon (133mXe, 135Xe, 135mXe, 137Xe, 138Xe, and 139Xe) resulting from 14 MeV neutron induced fission of depleted uranium at the National Ignition Facility. Measurements begin approximately 20 s after shot time, and yields have been determined for nuclides with half-lives as short as tens of seconds. We determined the relative independent yields of 133mXe, 135Xe, and 135mXe to significantly higher precision than previously reported. The relative fission yields of all nuclides are statistically indistinguishable from values reported by England and Rider (ENDF-349. LA-UR-94-3106, 1994), with exception of the cumulative yield of 139Xe. Furthermore, considerable differencesmore » exist between our measured yields and the JEFF-3.1 database values.« less

  4. STEM-EDS analysis of fission products in neutron-irradiated TRISO fuel particles from AGR-1 experiment

    NASA Astrophysics Data System (ADS)

    Leng, B.; van Rooyen, I. J.; Wu, Y. Q.; Szlufarska, I.; Sridharan, K.

    2016-07-01

    Historic and recent post-irradiation-examination from the German AVR and Advanced Gas Reactor Fuel Development and Qualification Project have shown that 110 m Ag is released from intact tristructural isotropic (TRISO) fuel. Although TRISO fuel particle research has been performed over the last few decades, little is known about how metallic fission products are transported through the SiC layer, and it was not until March 2013 that Ag was first identified in the SiC layer of a neutron-irradiated TRISO fuel particle. The existence of Pd- and Ag-rich grain boundary precipitates, triple junction precipitates, and Pd nano-sized intragranular precipitates in neutron-irradiated TRISO particle coatings was investigated using Scanning Transmission Electron Microscopy and Energy Dispersive Spectroscopy analysis to obtain more information on the chemical composition of the fission product precipitates. A U-rich fission product honeycomb shape precipitate network was found near a micron-sized precipitate in a SiC grain about ∼5 μm from the SiC-inner pyrolytic carbon interlayer, indicating a possible intragranular transport path for uranium. A single Ag-Pd nano-sized precipitate was found inside a SiC grain, and this is the first research showing such finding in irradiated SiC. This finding may possibly suggest a possible Pd-assisted intragranular transport mechanism for Ag and may be related to void or dislocation networks inside SiC grains. Preliminary semi-quantitative analysis indicated the micron-sized precipitates to be Pd2Si2U with carbon existing inside these precipitates. However, the results of such analysis for nano-sized precipitates may be influenced by the SiC matrix. The results reported in this paper confirm the co-existence of Cd with Ag in triple points reported previously.

  5. An Approach for Validating Actinide and Fission Product Burnup Credit Criticality Safety Analyses: Criticality (keff) Predictions

    DOE PAGES

    Scaglione, John M.; Mueller, Don E.; Wagner, John C.

    2014-12-01

    One of the most important remaining challenges associated with expanded implementation of burnup credit in the United States is the validation of depletion and criticality calculations used in the safety evaluation—in particular, the availability and use of applicable measured data to support validation, especially for fission products (FPs). Applicants and regulatory reviewers have been constrained by both a scarcity of data and a lack of clear technical basis or approach for use of the data. In this study, this paper describes a validation approach for commercial spent nuclear fuel (SNF) criticality safety (keff) evaluations based on best-available data and methodsmore » and applies the approach for representative SNF storage and transport configurations/conditions to demonstrate its usage and applicability, as well as to provide reference bias results. The criticality validation approach utilizes not only available laboratory critical experiment (LCE) data from the International Handbook of Evaluated Criticality Safety Benchmark Experiments and the French Haut Taux de Combustion program to support validation of the principal actinides but also calculated sensitivities, nuclear data uncertainties, and limited available FP LCE data to predict and verify individual biases for relevant minor actinides and FPs. The results demonstrate that (a) sufficient critical experiment data exist to adequately validate keff calculations via conventional validation approaches for the primary actinides, (b) sensitivity-based critical experiment selection is more appropriate for generating accurate application model bias and uncertainty, and (c) calculated sensitivities and nuclear data uncertainties can be used for generating conservative estimates of bias for minor actinides and FPs. Results based on the SCALE 6.1 and the ENDF/B-VII.0 cross-section libraries indicate that a conservative estimate of the bias for the minor actinides and FPs is 1.5% of their worth within the

  6. Comparison of predicted and measured fission product behavior in the Fort St. Vrain HTGR during the first three cycles of operation

    SciTech Connect

    Hanson, D.L.; Jovanovic, V.; Burnette, R.D.

    1985-10-01

    Fission product release from the reactor core has been predicted by the reference design methods and compared with reactor surveillance measurements and with the results of postirradiation examination (PIE) of spent FSV fuel elements. Overall, the predictive methods have been shown to be conservative: the predicted fission gas release at the end of Cycle 3 is about five times higher than observed. The dominant source of fission gas release is as-manufactured, heavy-metal contamination; in-service failure of the coated fuel particles appears to be negligible which is consistent with the PIE of spent fuel elements removed during the first two refuelings. The predicted releases of fission metals are insignificant compared to the release and subsequent decay of their gaseous precursors which is consistent with plateout probe measurements.

  7. Use of Information Theory Concepts for Developing Contaminated Site Detection Method: Case for Fission Product and Actinides Accumulation Modeling

    SciTech Connect

    Harbachova, N.V.; Sharavarau, H.A.

    2006-07-01

    Information theory concepts and their fundamental importance for environmental pollution analysis in light of experience of Chernobyl accident in Belarus are discussed. An information and dynamic models of the radionuclide composition formation in the fuel of the Nuclear Power Plant are developed. With the use of code DECA numerical calculation of actinides (58 isotopes are included) and fission products (650 isotopes are included) activities has been carried out and their dependence with the fuel burn-up of the RBMK-type reactor have been investigated. (authors)

  8. Gas-phase detection of solid-state fission product complexes for post-detonation nuclear forensic analysis.

    PubMed

    Stratz, S Adam; Jones, Steven A; Oldham, Colton J; Mullen, Austin D; Jones, Ashlyn V; Auxier, John D; Hall, Howard L

    2016-01-01

    This study presents the first known detection of fission products commonly found in post-detonation nuclear debris samples using solid sample introduction and a uniquely coupled gas chromatography inductively-coupled plasma time-of-flight mass spectrometer. Rare earth oxides were chemically altered to incorporate a ligand that enhances the volatility of the samples. These samples were injected (as solids) into the aforementioned instrument and detected for the first time. Repeatable results indicate the validity of the methodology, and this capability, when refined, will prove to be a valuable asset for rapid post-detonation nuclear forensic analysis.

  9. Mitochondrial fusion but not fission regulates larval growth and synaptic development through steroid hormone production.

    PubMed

    Sandoval, Hector; Yao, Chi-Kuang; Chen, Kuchuan; Jaiswal, Manish; Donti, Taraka; Lin, Yong Qi; Bayat, Vafa; Xiong, Bo; Zhang, Ke; David, Gabriela; Charng, Wu-Lin; Yamamoto, Shinya; Duraine, Lita; Graham, Brett H; Bellen, Hugo J

    2014-10-14

    Mitochondrial fusion and fission affect the distribution and quality control of mitochondria. We show that Marf (Mitochondrial associated regulatory factor), is required for mitochondrial fusion and transport in long axons. Moreover, loss of Marf leads to a severe depletion of mitochondria in neuromuscular junctions (NMJs). Marf mutants also fail to maintain proper synaptic transmission at NMJs upon repetitive stimulation, similar to Drp1 fission mutants. However, unlike Drp1, loss of Marf leads to NMJ morphology defects and extended larval lifespan. Marf is required to form contacts between the endoplasmic reticulum and/or lipid droplets (LDs) and for proper storage of cholesterol and ecdysone synthesis in ring glands. Interestingly, human Mitofusin-2 rescues the loss of LD but both Mitofusin-1 and Mitofusin-2 are required for steroid-hormone synthesis. Our data show that Marf and Mitofusins share an evolutionarily conserved role in mitochondrial transport, cholesterol ester storage and steroid-hormone synthesis.

  10. Comparison of various hours living fission products for absolute power density determination in VVER-1000 mock up in LR-0 reactor.

    PubMed

    Košťál, Michal; Švadlenková, Marie; Koleška, Michal; Rypar, Vojtěch; Milčák, Ján

    2015-11-01

    Measuring power level of zero power reactor is a quite difficult task. Due to the absence of measurable cooling media heating, it is necessary to employ a different method. The gamma-ray spectroscopy of fission products induced within reactor operation is one of possible ways of power determination. The method is based on the proportionality between fission product buildup and released power. The (92)Sr fission product was previously preferred as nuclide for LR-0 power determination for short-time irradiation experiments. This work aims to find more appropriate candidates, because the (92)Sr, however suitable, has a short half-life, which limits the maximal measurable amount of fuel pins within a single irradiation batch. The comparison of various isotopes is realized for (92)Sr, (97)Zr, (135)I, (91)Sr, and (88)Kr. The comparison between calculated and experimentally determined (C/E-1 values) net peak areas is assessed for these fission products. Experimental results show that studied fission products, except (88)Kr, are in comparable agreement with (92)Sr results. Since (91)Sr has notably higher half-life than (92)Sr, (91)Sr seems to be more appropriate marker in experiments with a large number of measured fuel pins.

  11. Cement As a Waste Form for Nuclear Fission Products: The Case of (90)Sr and Its Daughters.

    PubMed

    Dezerald, Lucile; Kohanoff, Jorge J; Correa, Alfredo A; Caro, Alfredo; Pellenq, Roland J-M; Ulm, Franz J; Saúl, Andrés

    2015-11-17

    One of the main challenges faced by the nuclear industry is the long-term confinement of nuclear waste. Because it is inexpensive and easy to manufacture, cement is the material of choice to store large volumes of radioactive materials, in particular the low-level medium-lived fission products. It is therefore of utmost importance to assess the chemical and structural stability of cement containing radioactive species. Here, we use ab initio calculations based on density functional theory (DFT) to study the effects of (90)Sr insertion and decay in C-S-H (calcium-silicate-hydrate) in order to test the ability of cement to trap and hold this radioactive fission product and to investigate the consequences of its β-decay on the cement paste structure. We show that (90)Sr is stable when it substitutes the Ca(2+) ions in C-S-H, and so is its daughter nucleus (90)Y after β-decay. Interestingly, (90)Zr, daughter of (90)Y and final product in the decay sequence, is found to be unstable compared to the bulk phase of the element at zero K but stable when compared to the solvated ion in water. Therefore, cement appears as a suitable waste form for (90)Sr storage.

  12. Glass Ceramic Waste Forms for Combined CS+LN+TM Fission Products Waste Streams

    SciTech Connect

    Crum, Jarrod V.; Turo, Laura A.; Riley, Brian J.; Tang, Ming; Kossoy, Anna; Sickafus, Kurt E.

    2010-09-23

    In this study, glass ceramics were explored as an alternative waste form for glass, the current baseline, to be used for immobilizing alkaline/alkaline earth + lanthanide (CS+LN) or CS+LN+transition metal (TM) fission-product waste streams generated by a uranium extraction (UREX+) aqueous separations type process. Results from past work on a glass waste form for the combined CS+LN waste streams showed that as waste loading increased, large fractions of crystalline phases precipitated upon slow cooling.[1] The crystalline phases had no noticeable impact on the waste form performance by the 7-day product consistency test (PCT). These results point towards the development of a glass ceramic waste form for treating CS+LN or CS+LN+TM combined waste streams. Three main benefits for exploring glass ceramics are: (1) Glass ceramics offer increased solubility of troublesome components in crystalline phases as compared to glass, leading to increased waste loading; (2) The crystalline network formed in the glass ceramic results in higher heat tolerance than glass; and (3) These glass ceramics are designed to be processed by the same melter technology as the current baseline glass waste form. It will only require adding controlled canister cooling for crystallization into a glass ceramic waste form. Highly annealed waste form (essentially crack free) with up to 50X lower surface area than a typical High-Level Waste (HLW) glass canister. Lower surface area translates directly into increased durability. This was the first full year of exploring glass ceramics for the Option 1 and 2 combined waste stream options. This work has shown that dramatic increases in waste loading are achievable by designing a glass ceramic waste form as an alternative to glass. Table S1 shows the upper limits for heat, waste loading (based on solubility), and the decay time needed before treatment can occur for glass and glass ceramic waste forms. The improvements are significant for both combined waste

  13. ENDF/B-VII.1 Nuclear Data for Science and Technology: Cross Sections, Covariances, Fission Product Yields and Decay Data

    SciTech Connect

    Chadwick, M.B.; Herman, M.; Author : Chadwick,M.B.; Herman,M.; Oblozinsky,P.; Dunn,M.E.; Danon,Y.; Kahler,A.C.; Smith,D.L.; Pritychenko,B.; Arbanas,G.; Arcilla,R.; Brewer,R.; Brown,D.A.; Capote,R.; Carlson,A.D.; Cho,Y.S.; Derrien,H.; Guber,K.; Hale,G.M.; Hoblit,S.; Holloway,S.: Johnson,T.D.; Kawano,T.; Kiedrowski,B.C.; Kim,H.; Kunieda,S.; Larson,N.M.; Leal,L.; Lestone,J.P.; Little,R.C.; McCutchan,E.A.; MacFarlane,R.E.; MacInnes,M.; Mattoon,C.M.; McKnight,R.D.; Mughabghab,S.F.; Nobre,G.P.A.; Palmiotti,G.; Palumbo,A.; Pigni,M.T.; Pronyaev,V.G.; Sayer,R.O.; Sonzogni,A.A.; Summers,N.C.; Talou,P.; Thompson,I.J.; Trkov,A.; Vogt,R.L.; van der Marck,S.C.; Wallner,A.; White,M.C.; Wiarda,D.; Young,P.G.

    2011-12-01

    The ENDF/B-VII.1 library is our latest recommended evaluated nuclear data file for use in nuclear science and technology applications, and incorporates advances made in the five years since the release of ENDF/B-VII.0. These advances focus on neutron cross sections, covariances, fission product yields and decay data, and represent work by the US Cross Section Evaluation Working Group (CSEWG) in nuclear data evaluation that utilizes developments in nuclear theory, modeling, simulation, and experiment. The principal advances in the new library are: (1) An increase in the breadth of neutron reaction cross section coverage, extending from 393 nuclides to 423 nuclides; (2) Covariance uncertainty data for 190 of the most important nuclides, as documented in companion papers in this edition; (3) R-matrix analyses of neutron reactions on light nuclei, including isotopes of He, Li, and Be; (4) Resonance parameter analyses at lower energies and statistical high energy reactions for isotopes of Cl, K, Ti, V, Mn, Cr, Ni, Zr and W; (5) Modifications to thermal neutron reactions on fission products (isotopes of Mo, Tc, Rh, Ag, Cs, Nd, Sm, Eu) and neutron absorber materials (Cd, Gd); (6) Improved minor actinide evaluations for isotopes of U, Np, Pu, and Am (we are not making changes to the major actinides {sup 235,238}U and {sup 239}Pu at this point, except for delayed neutron data and covariances, and instead we intend to update them after a further period of research in experiment and theory), and our adoption of JENDL-4.0 evaluations for isotopes of Cm, Bk, Cf, Es, Fm, and some other minor actinides; (7) Fission energy release evaluations; (8) Fission product yield advances for fission-spectrum neutrons and 14 MeV neutrons incident on {sup 239}Pu; and (9) A new decay data sublibrary. Integral validation testing of the ENDF/B-VII.1 library is provided for a variety of quantities: For nuclear criticality, the VII.1 library maintains the generally-good performance seen for VII.0

  14. ENDF/B-VII.1 Nuclear Data for Science and Technology: Cross Sections, Covariances, Fission Product Yields and Decay Data

    SciTech Connect

    Chadwick, M. B.; Herman, Micheal W; Oblozinsky, Pavel; Dunn, Michael E; Danon, Y.; Kahler, A.; Smith, Donald L.; Pritychenko, B; Arbanas, Goran; Arcilla, r; Brewer, R; Brown, D A; Capote, R.; Carlson, A. D.; Cho, Y S; Derrien, Herve; Guber, Klaus H; Hale, G. M.; Hoblit, S; Holloway, Shannon T.; Johnson, T D; Kawano, T.; Kiedrowski, B C; Kim, H; Kunieda, S; Larson, Nancy M; Leal, Luiz C; Lestone, J P; Little, R C; Mccutchan, E A; Macfarlane, R E; MacInnes, M; Matton, C M; Mcknight, R D; Mughabghab, S F; Nobre, G P; Palmiotti, G; Palumbo, A; Pigni, Marco T; Pronyaev, V. G.; Sayer, Royce O; Sonzogni, A A; Summers, N C; Talou, P; Thompson, I J; Trkov, A.; Vogt, R L; Van der Marck, S S; Wallner, A; White, M C; Wiarda, Dorothea; Young, P C

    2011-01-01

    The ENDF/B-VII.1 library is our latest recommended evaluated nuclear data file for use in nuclear science and technology applications, and incorporates advances made in the five years since the release of ENDF/B-VII.0. These advances focus on neutron cross sections, covariances, fission product yields and decay data, and represent work by the US Cross Section Evaluation Working Group (CSEWG) in nuclear data evaluation that utilizes developments in nuclear theory, modeling, simulation, and experiment. The principal advances in the new library are: (1) An increase in the breadth of neutron reaction cross section coverage, extending from 393 nuclides to 423 nuclides; (2) Covariance uncertainty data for 190 of the most important nuclides, as documented in companion papers in this edition; (3) R-matrix analyses of neutron reactions on light nuclei, including isotopes of He; Li, and Be; (4) Resonance parameter analyses at lower energies and statistical high energy reactions for isotopes of Cl; K; Ti, V, Mn, Cr, Ni, Zr and W; (5) Modifications to thermal neutron reactions on fission products (isotopes of Mo, Tc, Rh, Ag, Cs, Nd, Sm, Eu) and neutron absorber materials (Cd, Gd); (6) Improved minor actinide evaluations for isotopes of U, Np, Pu, and Am (we are not making changes to the major actinides (235,238)U and (239)Pu at this point, except for delayed neutron data and covariances, and instead we intend to update them after a further period of research in experiment and theory), and our adoption of JENDL-4.0 evaluations for isotopes of Cm, Bk, Cf, Es; Fm; and some other minor actinides; (7) Fission energy release evaluations; (8) Fission product yield advances for fission-spectrum neutrons and 14 MeV neutrons incident on (239)Pu; and (9) A new decay data sublibrary. Integral validation testing of the ENDF/B-VII.1 library is provided for a variety of quantities: For nuclear criticality, the VII.1 library maintains the generally-good performance seen for VII.0 for a wide

  15. ENDF/B-VII.1 Nuclear Data for Science and Technology: Cross Sections, Covariances, Fission Product Yields and Decay Data

    NASA Astrophysics Data System (ADS)

    Chadwick, M. B.; Herman, M.; Obložinský, P.; Dunn, M. E.; Danon, Y.; Kahler, A. C.; Smith, D. L.; Pritychenko, B.; Arbanas, G.; Arcilla, R.; Brewer, R.; Brown, D. A.; Capote, R.; Carlson, A. D.; Cho, Y. S.; Derrien, H.; Guber, K.; Hale, G. M.; Hoblit, S.; Holloway, S.; Johnson, T. D.; Kawano, T.; Kiedrowski, B. C.; Kim, H.; Kunieda, S.; Larson, N. M.; Leal, L.; Lestone, J. P.; Little, R. C.; McCutchan, E. A.; MacFarlane, R. E.; MacInnes, M.; Mattoon, C. M.; McKnight, R. D.; Mughabghab, S. F.; Nobre, G. P. A.; Palmiotti, G.; Palumbo, A.; Pigni, M. T.; Pronyaev, V. G.; Sayer, R. O.; Sonzogni, A. A.; Summers, N. C.; Talou, P.; Thompson, I. J.; Trkov, A.; Vogt, R. L.; van der Marck, S. C.; Wallner, A.; White, M. C.; Wiarda, D.; Young, P. G.

    2011-12-01

    The ENDF/B-VII.1 library is our latest recommended evaluated nuclear data file for use in nuclear science and technology applications, and incorporates advances made in the five years since the release of ENDF/B-VII.0. These advances focus on neutron cross sections, covariances, fission product yields and decay data, and represent work by the US Cross Section Evaluation Working Group (CSEWG) in nuclear data evaluation that utilizes developments in nuclear theory, modeling, simulation, and experiment. The principal advances in the new library are: (1) An increase in the breadth of neutron reaction cross section coverage, extending from 393 nuclides to 423 nuclides; (2) Covariance uncertainty data for 190 of the most important nuclides, as documented in companion papers in this edition; (3) R-matrix analyses of neutron reactions on light nuclei, including isotopes of He, Li, and Be; (4) Resonance parameter analyses at lower energies and statistical high energy reactions for isotopes of Cl, K, Ti, V, Mn, Cr, Ni, Zr and W; (5) Modifications to thermal neutron reactions on fission products (isotopes of Mo, Tc, Rh, Ag, Cs, Nd, Sm, Eu) and neutron absorber materials (Cd, Gd); (6) Improved minor actinide evaluations for isotopes of U, Np, Pu, and Am (we are not making changes to the major actinides 235,238U and 239Pu at this point, except for delayed neutron data and covariances, and instead we intend to update them after a further period of research in experiment and theory), and our adoption of JENDL-4.0 evaluations for isotopes of Cm, Bk, Cf, Es, Fm, and some other minor actinides; (7) Fission energy release evaluations; (8) Fission product yield advances for fission-spectrum neutrons and 14 MeV neutrons incident on 239Pu; and (9) A new decay data sublibrary. Integral validation testing of the ENDF/B-VII.1 library is provided for a variety of quantities: For nuclear criticality, the VII.1 library maintains the generally-good performance seen for VII.0 for a wide range

  16. Spontaneous Fission

    DOE R&D Accomplishments Database

    Segre, Emilio

    1950-11-22

    The first attempt to discover spontaneous fission in uranium was made by [Willard] Libby, who, however, failed to detect it on account of the smallness of effect. In 1940, [K. A.] Petrzhak and [G. N.] Flerov, using more sensitive methods, discovered spontaneous fission in uranium and gave some rough estimates of the spontaneous fission decay constant of this substance. Subsequently, extensive experimental work on the subject has been performed by several investigators and will be quoted in the various sections. [N.] Bohr and [A.] Wheeler have given a theory of the effect based on the usual ideas of penetration of potential barriers. On this project spontaneous fission has been studied for the past several years in an effort to obtain a complete picture of the phenomenon. For this purpose the spontaneous fission decay constants {lambda} have been measured for separated isotopes of the heavy elements wherever possible. Moreover, the number {nu} of neutrons emitted per fission has been measured wherever feasible, and other characteristics of the spontaneous fission process have been studied. This report summarizes the spontaneous fission work done at Los Alamos up to January 1, 1945. A chronological record of the work is contained in the Los Alamos monthly reports.

  17. Summary Report: Glass-Ceramic Waste Forms for Combined Fission Products

    SciTech Connect

    Crum, Jarrod V.; Riley, Brian J.; Turo, Laura A.; Tang, Ming; Kossoy, Anna

    2011-09-23

    Glass-ceramic waste form development began in FY 2010 examining two combined waste stream options: (1) alkaline earth (CS) + lanthanide (Ln), and (2) + transition metal (TM) fission-product waste streams generated by the uranium extraction (UREX+) separations process. Glass-ceramics were successfully developed for both options however; Option 2 was selected over Option 1, at the conclusion of 2010, because Option 2 immobilized all three waste streams with only a minimal decrease in waste loading. During the first year, a series of three glass (Option 2) were fabricated that varied waste loading-WL (42, 45, and 50 mass%) at fixed molar ratios of CaO/MoO{sub 3} and B{sub 2}O{sub 3}/alkali both at 1.75. These glass-ceramics were slow cooled and characterized in terms of phase assemblage and preliminary irradiation stability. This fiscal year, further characterization was performed on the FY 2010 Option 2 glass-ceramics in terms of: static leach testing, phase analysis by transmission electron microscopy (TEM), and irradiation stability (electron and ion). Also, a new series of glass-ceramics were developed for Option 2 that varied the additives: Al{sub 2}O{sub 3} (0-6 mass%), molar ratio of CaO/MoO{sub 3} and B{sub 2}O{sub 3}/alkali (1.75 to 2.25) and waste loading (50, 55, and 60 mass%). Lastly, phase pure powellite and oxyapatite were synthesized for irradiation studies. Results of this fiscal year studies showed compositional flexibility, chemical stability, and radiation stability in the current glass-ceramic system. First, the phase assemblages and microstructure of all of the FY 2010 and 2011 glass-ceramics are very similar once subjected to the slow cool heat treatment. The phases identified in these glass-ceramics were oxyapatite, powellite, cerianite, and ln-borosilicate. This shows that variations in waste loading or additives can be accommodated without drastically changing the phase assemblage of the waste form, thus making the processing and performance

  18. True ternary fission

    NASA Astrophysics Data System (ADS)

    Vijayaraghavan, K. R.; Balasubramaniam, M.; von Oertzen, W.

    2015-04-01

    The study of the ternary fission of nuclei has received new interest recently. It is of general interest for nuclear dynamics, although the process is very rare. In the present work, we discuss the possibilities of true ternary fission (fragment masses A >30 ) in 252Cf for different mass splits. These mass splits are strongly favored in a collinear geometry. Based on the three cluster model (TCM), it is shown that the true ternary fission into fragments with almost equal masses is one of the possible fission modes in 252Cf . For general decays it is shown that the formation of the lightest fragment at the center has the highest probability. Further the formation of tin isotopes and/or other closed shell fragments are favored. For the decay products the presence of closed shell nuclei among the three fragments enhances the decay probabilities.

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

    SciTech Connect

    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.

  20. Formation of (Cr, Al)UO4 from doped UO2 and its influence on partition of soluble fission products

    NASA Astrophysics Data System (ADS)

    Cooper, M. W. D.; Gregg, D. J.; Zhang, Y.; Thorogood, G. J.; Lumpkin, G. R.; Grimes, R. W.; Middleburgh, S. C.

    2013-11-01

    CrUO4 and (Cr, Al)UO4 have been fabricated by a sol-gel method, studied using diffraction techniques and modelled using empirical pair potentials. Cr2O3 was predicted to preferentially form CrUO4 over entering solution into hyper-stoichiometric UO2+x by atomic scale simulation. Further, it was predicted that the formation of CrUO4 can proceed by removing excess oxygen from the UO2 lattice. Attempts to synthesise AlUO4 failed, instead forming U3O8 and Al2O3. X-ray diffraction confirmed the structure of CrUO4 and identifies the existence of a (Cr, Al)UO4 phase for the first time (with a maximum Al to Cr mole ratio of 1:3). Simulation was subsequently used to predict the partition energies for the removal of fission products or fuel additives from hyper-stoichiometric UO2+x and their incorporation into the secondary phase. The partition energies are consistent only with smaller cations (e.g. Zr4+, Mo4+ and Fe3+) residing in CrUO4, while all divalent cations are predicted to remain in UO2+x. Additions of Al had little effect on partition behaviour. The reduction of UO2+x due to the formation of CrUO4 has important implications for the solution limits of other fission products as many species are less soluble in UO2 than UO2+x.

  1. Volatile fission product behaviour during thermal annealing of irradiated UO 2 fuel oxidised up to U 3O 8

    NASA Astrophysics Data System (ADS)

    Hiernaut, J.-P.; Wiss, T.; Papaioannou, D.; Konings, R. J. M.; Rondinella, V. V.

    2008-01-01

    The behaviour and release of fission products during high-temperature annealing of irradiated UO 2 samples have been studied as a function of the oxidation state. The behaviour of a sample pre-oxidised to U 3O 8 was compared to that of non-pre-treated fuel from the same pellet radial location. The Knudsen cell mass spectrometer technique was used up to 1900 K for the pre-oxidised sample and up to 2800 K for the untreated sample. Both types of tests were run in vacuum. The possible chemical forms of the different fission products in the bulk and in the vapour phase have been estimated from the release curves and microprobe analysis. This study concerns essentially iodine, tellurium, caesium, rubidium, strontium, barium, technetium and molybdenum, whose effusion behaviour was strongly affected by the pre-oxidation treatment, resulting in an almost complete release by 1900 K. Release of zirconium, the lanthanides and actinides was observed at temperatures >1900 K, reached only in the case of the non-pre-treated UO 2 experiments.

  2. Stochastic simulation of fission product activity in primary coolant due to fuel rod failures in typical PWRs under power transients

    NASA Astrophysics Data System (ADS)

    Iqbal, M. Javed; Mirza, Nasir M.; Mirza, Sikander M.

    2008-01-01

    During normal operation of PWRs, routine fuel rods failures result in release of radioactive fission products (RFPs) in the primary coolant of PWRs. In this work, a stochastic model has been developed for simulation of failure time sequences and release rates for the estimation of fission product activity in primary coolant of a typical PWR under power perturbations. In the first part, a stochastic approach is developed, based on generation of fuel failure event sequences by sampling the time dependent intensity functions. Then a three-stage model based deterministic methodology of the FPCART code has been extended to include failure sequences and random release rates in a computer code FPCART-ST, which uses state-of-the-art LEOPARD and ODMUG codes as its subroutines. The value of the 131I activity in primary coolant predicted by FPCART-ST code has been found in good agreement with the corresponding values measured at ANGRA-1 nuclear power plant. The predictions of FPCART-ST code with constant release option have also been found to have good agreement with corresponding experimental values for time dependent 135I, 135Xe and 89Kr concentrations in primary coolant measured during EDITHMOX-1 experiments.

  3. Fission yield measurements at IGISOL

    NASA Astrophysics Data System (ADS)

    Lantz, M.; Al-Adili, A.; Gorelov, D.; Jokinen, A.; Kolhinen, V. S.; Mattera, A.; Moore, I.; Penttilä, H.; Pomp, S.; Prokofiev, A. V.; Rakopoulos, V.; Rinta-Antila, S.; Simutkin, V.; Solders, A.

    2016-06-01

    The fission product yields are an important characteristic of the fission process. In fundamental physics, knowledge of the yield distributions is needed to better understand the fission process. For nuclear energy applications good knowledge of neutroninduced fission-product yields is important for the safe and efficient operation of nuclear power plants. With the Ion Guide Isotope Separator On-Line (IGISOL) technique, products of nuclear reactions are stopped in a buffer gas and then extracted and separated by mass. Thanks to the high resolving power of the JYFLTRAP Penning trap, at University of Jyväskylä, fission products can be isobarically separated, making it possible to measure relative independent fission yields. In some cases it is even possible to resolve isomeric states from the ground state, permitting measurements of isomeric yield ratios. So far the reactions U(p,f) and Th(p,f) have been studied using the IGISOL-JYFLTRAP facility. Recently, a neutron converter target has been developed utilizing the Be(p,xn) reaction. We here present the IGISOL-technique for fission yield measurements and some of the results from the measurements on proton induced fission. We also present the development of the neutron converter target, the characterization of the neutron field and the first tests with neutron-induced fission.

  4. Measurements of extinct fission products in nuclear bomb debris: Determination of the yield of the Trinity nuclear test 70 y later.

    PubMed

    Hanson, Susan K; Pollington, Anthony D; Waidmann, Christopher R; Kinman, William S; Wende, Allison M; Miller, Jeffrey L; Berger, Jennifer A; Oldham, Warren J; Selby, Hugh D

    2016-07-19

    This paper describes an approach to measuring extinct fission products that would allow for the characterization of a nuclear test at any time. The isotopic composition of molybdenum in five samples of glassy debris from the 1945 Trinity nuclear test has been measured. Nonnatural molybdenum isotopic compositions were observed, reflecting an input from the decay of the short-lived fission products (95)Zr and (97)Zr. By measuring both the perturbation of the (95)Mo/(96)Mo and (97)Mo/(96)Mo isotopic ratios and the total amount of molybdenum in the Trinity nuclear debris samples, it is possible to calculate the original concentrations of the (95)Zr and (97)Zr isotopes formed in the nuclear detonation. Together with a determination of the amount of plutonium in the debris, these measurements of extinct fission products allow for new estimates of the efficiency and yield of the historic Trinity test.

  5. Measurements of extinct fission products in nuclear bomb debris: Determination of the yield of the Trinity nuclear test 70 y later

    PubMed Central

    Hanson, Susan K.; Pollington, Anthony D.; Waidmann, Christopher R.; Kinman, William S.; Wende, Allison M.; Miller, Jeffrey L.; Berger, Jennifer A.; Oldham, Warren J.; Selby, Hugh D.

    2016-01-01

    This paper describes an approach to measuring extinct fission products that would allow for the characterization of a nuclear test at any time. The isotopic composition of molybdenum in five samples of glassy debris from the 1945 Trinity nuclear test has been measured. Nonnatural molybdenum isotopic compositions were observed, reflecting an input from the decay of the short-lived fission products 95Zr and 97Zr. By measuring both the perturbation of the 95Mo/96Mo and 97Mo/96Mo isotopic ratios and the total amount of molybdenum in the Trinity nuclear debris samples, it is possible to calculate the original concentrations of the 95Zr and 97Zr isotopes formed in the nuclear detonation. Together with a determination of the amount of plutonium in the debris, these measurements of extinct fission products allow for new estimates of the efficiency and yield of the historic Trinity test. PMID:27382169

  6. Quantification of Uncertainties due to 235,238U, 239,240,241Pu and Fission Products Nuclear Data Uncertainties for a PWR Fuel Assembly

    NASA Astrophysics Data System (ADS)

    da Cruz, D. F.; Rochman, D.; Koning, A. J.

    2014-04-01

    Uncertainty analysis on reactivity and discharged inventory for a typical PWR fuel element as a result of uncertainties in 235,238U, 239,240,241Pu, and fission products nuclear data was performed. The Total Monte-Carlo (TMC) method was applied using the deterministic transport code DRAGON. The nuclear data used in this study is from the JEFF-3.1 evaluations, with the exception of the nuclear data files for U, Pu and fission products isotopes, which are taken from the nuclear data library TENDL-2012. Results show that the calculated total uncertainty in keff (as result of uncertainties in nuclear data of the considered isotopes) is virtually independent on fuel burnp and amounts to 700 pcm. The uncertainties in inventory of the discharged fuel is dependent on the element considered and lies in the range 1-15% for most fission products, and is below 5% for the most important actinides.

  7. Measurements of extinct fission products in nuclear bomb debris: Determination of the yield of the Trinity nuclear test 70 y later

    DOE PAGES

    Hanson, Susan Kloek; Pollington, Anthony Douglas; Waidmann, Christopher Russell; ...

    2016-07-05

    This study describes an approach to measuring extinct fission products that would allow for the characterization of a nuclear test at any time. The isotopic composition of molybdenum in five samples of glassy debris from the 1945 Trinity nuclear test has been measured. Nonnatural molybdenum isotopic compositions were observed, reflecting an input from the decay of the short-lived fission products 95Zr and 97Zr. By measuring both the perturbation of the 95Mo/96Mo and 97Mo/96Mo isotopic ratios and the total amount of molybdenum in the Trinity nuclear debris samples, it is possible to calculate the original concentrations of the 95Zr and 97Zrmore » isotopes formed in the nuclear detonation. Together with a determination of the amount of plutonium in the debris, these measurements of extinct fission products allow for new estimates of the efficiency and yield of the historic Trinity test.« less

  8. Measuring and predicting the transport of actinides and fission product contaminants in unsaturated prairie soil

    NASA Astrophysics Data System (ADS)

    Sims, D. J.

    Soil samples have been taken in 2001 from the area of a 1951 release from an underground storage tank of 6.7 L of an aqueous solution of irradiated uranium (360 GBq). A simulation of the dispersion of the actinides and fission products was conducted in the laboratory using irradiated natural uranium, non-irradiated natural uranium and metal standards dissolved in acidic aqueous solutions and added to soil columns containing uncontaminated prairie soil. The lab soil columns were allowed 12 to 14 months for contaminant transport. Soil samples were analyzed using gamma-ray spectroscopy, neutron activation analysis (NAA) and liquid scintillation counting (LSC) to determine the elemental concentrations of U, Cs and Sr. Diffusion coefficients from the 50 year soil samples and the lab soil samples were determined. The measured diffusion coefficients from the field samples were 3.0 x 10-4 cm2 s-1 (Cs-137), 1.8 x 10-5 cm2 s-1 (U-238) and 2.6 x 10-3 cm2 s-1 (Sr-90) and the values determined from lab simulation were 5 x 10-6 cm 2 s-1 (Cs-137), 3 x 10-5 cm2 s-1 (U-238) and 1.9 x 10-5 cm 2 s-1 (Sr-90). The differences between the sets of diffusion coefficients can be attributed to differences in retardation effects, weather effects and changes in the soil characteristics when transporting, such as porosity. The analytical work showed that Cs-137 content of soil can be determined effectively using gamma-ray spectroscopy; U-238 content can be measured using NAA; and Sr-90 content can be measured using LSC. For non- and low-radioactive species, it was shown that both flame atomic absorption spectrometry (FAAS) and inductively-coupled plasma-mass spectrometry (ICP-MS) gave comparable results for Sr, Cs and Sm, with the average values ranging from 0.5 to 4.5 ppm of each other. The U-238 content results from NAA and from ICP-MS showed general agreement with an average difference of 81.3 ppm on samples having concentrations up to 988.2 ppm. The difference may have been due to matrix

  9. Assessment of Fission Product Cross-Section Data for Burnup Credit Applications

    SciTech Connect

    Leal, Luiz C; Derrien, Herve; Dunn, Michael E; Mueller, Don

    2007-12-01

    Past efforts by the Department of Energy (DOE), the Electric Power Research Institute (EPRI), the Nuclear Regulatory Commission (NRC), and others have provided sufficient technical information to enable the NRC to issue regulatory guidance for implementation of pressurized-water reactor (PWR) burnup credit; however, consideration of only the reactivity change due to the major actinides is recommended in the guidance. Moreover, DOE, NRC, and EPRI have noted the need for additional scientific and technical data to justify expanding PWR burnup credit to include fission product (FP) nuclides and enable burnup credit implementation for boiling-water reactor (BWR) spent nuclear fuel (SNF). The criticality safety assessment needed for burnup credit applications will utilize computational analyses of packages containing SNF with FP nuclides. Over the years, significant efforts have been devoted to the nuclear data evaluation of major isotopes pertinent to reactor applications (i.e., uranium, plutonium, etc.); however, efforts to evaluate FP cross-section data in the resonance region have been less thorough relative to actinide data. In particular, resonance region cross-section measurements with corresponding R-matrix resonance analyses have not been performed for FP nuclides. Therefore, the objective of this work is to assess the status and performance of existing FP cross-section and cross-section uncertainty data in the resonance region for use in burnup credit analyses. Recommendations for new cross-section measurements and/or evaluations are made based on the data assessment. The assessment focuses on seven primary FP isotopes (103Rh, 133Cs, 143Nd, 149Sm, 151Sm, 152Sm, and 155Gd) that impact reactivity analyses of transportation packages and two FP isotopes (153Eu and 155Eu) that impact prediction of 155Gd concentrations. Much of the assessment work was completed in 2005, and the assessment focused on the latest FP cross-section evaluations available in the

  10. Solar vs. Fission Surface Power for Mars

    NASA Technical Reports Server (NTRS)

    Rucker, Michelle A.; Oleson, Steve; George, Pat; Landis, Geoffrey A.; Fincannon, James; Bogner, Amee; Jones, Robert E.; Turnbull, Elizabeth; Martini, Michael C.; Gyekenyesi, John Z.; hide

    2016-01-01

    A multi-discipline team of experts from the National Aeronautics and Space Administration (NASA) developed Mars surface power system point design solutions for two conceptual missions. The primary goal of this study was to compare the relative merits of solar- versus fission-powered versions of each surface mission. First, the team compared three different solar power options against a fission power system concept for a sub-scale, uncrewed demonstration mission. The 4.5 meter (m) diameter pathfinder lander's primary mission would be to demonstrate Mars entry, descent, and landing techniques. Once on the Martian surface, the lander's In Situ Resource Utilization (ISRU) payload would demonstrate liquid oxygen propellant production using atmospheric resources. For the purpose of this exercise, location was assumed to be at the Martian equator. The three solar concepts considered included a system that only operated during daylight hours (at roughly half the daily propellant production rate of a round-the-clock fission design), a battery-augmented system that operated through the night (matching the fission concept's propellant production rate), and a system that operated only during daylight, but at a higher rate (again, matching the fission concept's propellant production rate). Including 30% mass growth allowance, total payload masses for the three solar concepts ranged from 1,116 to 2,396 kg, versus the 2,686 kg fission power scheme. However, solar power masses are expected to approach or exceed the fission payload mass at landing sites further from the equator, making landing site selection a key driver in the final power system decision. The team also noted that detailed reliability analysis should be performed on daytime-only solar power schemes to assess potential issues with frequent ISRU system on/off cycling. Next, the team developed a solar-powered point design solution for a conceptual four-crew, 500-day surface mission consisting of up to four landers per

  11. Determination of gaseous fission product yields from 14 MeV neutron induced fission of 238U at the National Ignition Facility

    SciTech Connect

    Cassata, W. S.; Velsko, C. A.; Stoeffl, W.; Jedlovec, D. R.; Golod, A. B.; Shaughnessy, D. A.; Yeamans, C. B.; Edwards, E. R.; Schneider, D. H. G.

    2016-01-14

    We determined fission yields of xenon (133mXe, 135Xe, 135mXe, 137Xe, 138Xe, and 139Xe) resulting from 14 MeV neutron induced fission of depleted uranium at the National Ignition Facility. Measurements begin approximately 20 s after shot time, and yields have been determined for nuclides with half-lives as short as tens of seconds. We determined the relative independent yields of 133mXe, 135Xe, and 135mXe to significantly higher precision than previously reported. The relative fission yields of all nuclides are statistically indistinguishable from values reported by England and Rider (ENDF-349. LA-UR-94-3106, 1994), with exception of the cumulative yield of 139Xe. Furthermore, considerable differences exist between our measured yields and the JEFF-3.1 database values.

  12. Neutronic and thermal-hydraulic analysis of fission molybdenum-99 production at Tehran Research Reactor using LEU plate targets.

    PubMed

    Abedi, Ebrahim; Ebrahimkhani, Marzieh; Davari, Amin; Mirvakili, Seyed Mohammad; Tabasi, Mohsen; Maragheh, Mohammad Ghannadi

    2016-12-01

    Efficient and safe production of molybdenum-99 ((99)Mo) radiopharmaceutical at Tehran Research Reactor (TRR) via fission of LEU targets is studied. Neutronic calculations are performed to evaluate produced (99)Mo activity, core neutronic safety parameters and also the power deposition values in target plates during a 7 days irradiation interval. Thermal-hydraulic analysis has been also carried out to obtain thermal behavior of these plates. Using Thermal-hydraulic analysis, it can be concluded that the safety parameters are satisfied in the current study. Consequently, the present neutronic and thermal-hydraulic calculations show efficient (99)Mo production is accessible at significant activity values in TRR current core configuration. Copyright © 2016 Elsevier Ltd. All rights reserved.

  13. Spectroscopy of few-particle nuclei around magic {sup 132}Sn from fission product {gamma}-ray studies.

    SciTech Connect

    Zhang, C. T.

    1998-07-29

    We are studying the yrast structure of very neutron-rich nuclei around doubly magic {sup 132}Sn by analyzing fission product {gamma}-ray data from a {sup 248}Cm source at Eurogam II. Yrast cascades in several few-valence-particle nuclei have been identified through {gamma}{gamma} cross coincidences with their complementary fission partners. Results for two-valence-particle nuclei {sup 132}Sb, {sup 134}Te, {sup 134}Sb and {sup 134}Sn provide empirical nucleon-nucleon interactions which, combined with single-particle energies already known in the one-particle nuclei, are essential for shell-model analysis in this region. Findings for the N = 82 nuclei {sup 134}Te and {sup 135}I have now been extended to the four-proton nucleus {sup 136}Xe. Results for the two-neutron nucleus {sup 134}Sn and the N = 83 isotones {sup 134}Sb, {sup 135}Te and {sup 135}I open up the spectroscopy of nuclei in the northeast quadrant above {sup 132}Sn.

  14. Parallel computation safety analysis irradiation targets fission product molybdenum in neutronic aspect using the successive over-relaxation algorithm

    SciTech Connect

    Susmikanti, Mike; Dewayatna, Winter; Sulistyo, Yos

    2014-09-30

    One of the research activities in support of commercial radioisotope production program is a safety research on target FPM (Fission Product Molybdenum) irradiation. FPM targets form a tube made of stainless steel which contains nuclear-grade high-enrichment uranium. The FPM irradiation tube is intended to obtain fission products. Fission materials such as Mo{sup 99} used widely the form of kits in the medical world. The neutronics problem is solved using first-order perturbation theory derived from the diffusion equation for four groups. In contrast, Mo isotopes have longer half-lives, about 3 days (66 hours), so the delivery of radioisotopes to consumer centers and storage is possible though still limited. The production of this isotope potentially gives significant economic value. The criticality and flux in multigroup diffusion model was calculated for various irradiation positions and uranium contents. This model involves complex computation, with large and sparse matrix system. Several parallel algorithms have been developed for the sparse and large matrix solution. In this paper, a successive over-relaxation (SOR) algorithm was implemented for the calculation of reactivity coefficients which can be done in parallel. Previous works performed reactivity calculations serially with Gauss-Seidel iteratives. The parallel method can be used to solve multigroup diffusion equation system and calculate the criticality and reactivity coefficients. In this research a computer code was developed to exploit parallel processing to perform reactivity calculations which were to be used in safety analysis. The parallel processing in the multicore computer system allows the calculation to be performed more quickly. This code was applied for the safety limits calculation of irradiated FPM targets containing highly enriched uranium. The results of calculations neutron show that for uranium contents of 1.7676 g and 6.1866 g (× 10{sup 6} cm{sup −1}) in a tube, their delta

  15. Ionizing radiation accelerates Drp1-dependent mitochondrial fission, which involves delayed mitochondrial reactive oxygen species production in normal human fibroblast-like cells.

    PubMed

    Kobashigawa, Shinko; Suzuki, Keiji; Yamashita, Shunichi

    2011-11-04

    Ionizing radiation is known to increase intracellular level of reactive oxygen species (ROS) through mitochondrial dysfunction. Although it has been as a basis of radiation-induced genetic instability, the mechanism involving mitochondrial dysfunction remains unclear. Here we studied the dynamics of mitochondrial structure in normal human fibroblast like cells exposed to ionizing radiation. Delayed mitochondrial O(2)(-) production was peaked 3 days after irradiation, which was coupled with accelerated mitochondrial fission. We found that radiation exposure accumulated dynamin-related protein 1 (Drp1) to mitochondria. Knocking down of Drp1 expression prevented radiation induced acceleration of mitochondrial fission. Furthermore, knockdown of Drp1 significantly suppressed delayed production of mitochondrial O(2)(-). Since the loss of mitochondrial membrane potential, which was induced by radiation was prevented in cells knocking down of Drp1 expression, indicating that the excessive mitochondrial fission was involved in delayed mitochondrial dysfunction after irradiation.

  16. MELCOR 1.8.5 modeling aspects of fission product release, transport and deposition an assessment with recommendations.

    SciTech Connect

    Gauntt, Randall O.

    2010-04-01

    The Phebus and VERCORS data have played an important role in contemporary understanding and modeling of fission product release and transport from damaged light water reactor fuel. The data from these test programs have allowed improvement of MELCOR modeling of release and transport processes for both low enrichment uranium fuel as well as high burnup and mixed oxide (MOX) fuels. This paper discusses the synthesis of these findings in the MELCOR severe accident code. Based on recent assessments of MELCOR 1.8.5 fission product release modeling against the Phebus FPT-1 test and on observations from the ISP-46 exercise, modifications to the default MELCOR 1.8.5 release models are recommended. The assessments identified an alternative set of Booth diffusion parameters recommended by ORNL (ORNL-Booth), which produced significantly improved release predictions for cesium and other fission product groups. Some adjustments to the scaling factors in the ORNL-Booth model were made for selected fission product groups, including UO{sub 2}, Mo and Ru in order to obtain better comparisons with the FPT-1 data. The adjusted model, referred to as 'Modified ORNL-Booth,' was subsequently compared to original ORNL VI fission product release experiments and to more recently performed French VERCORS tests, and the comparisons was as favorable or better than the original CORSOR-M MELCOR default release model. These modified ORNL-Booth parameters, input to MELCOR 1.8.5 as 'sensitivity coefficients' (i.e. user input that over-rides the code defaults) are recommended for the interim period until improved release models can be implemented into MELCOR. For the case of ruthenium release in air-oxidizing conditions, some additional modifications to the Ru class vapor pressure are recommended based on estimates of the RuO{sub 2} vapor pressure over mildly hyperstoichiometric UO{sub 2}. The increased vapor pressure for this class significantly increases the net transport of Ru from the fuel to

  17. An Approach for Validating Actinide and Fission Product Burnup Credit Criticality Safety Analyses--Criticality (keff) Predictions

    SciTech Connect

    Scaglione, John M; Mueller, Don; Wagner, John C

    2011-01-01

    One of the most significant remaining challenges associated with expanded implementation of burnup credit in the United States is the validation of depletion and criticality calculations used in the safety evaluation - in particular, the availability and use of applicable measured data to support validation, especially for fission products. Applicants and regulatory reviewers have been constrained by both a scarcity of data and a lack of clear technical basis or approach for use of the data. U.S. Nuclear Regulatory Commission (NRC) staff have noted that the rationale for restricting their Interim Staff Guidance on burnup credit (ISG-8) to actinide-only is based largely on the lack of clear, definitive experiments that can be used to estimate the bias and uncertainty for computational analyses associated with using burnup credit. To address the issue of validation, the NRC initiated a project with the Oak Ridge National Laboratory to (1) develop and establish a technically sound validation approach (both depletion and criticality) for commercial spent nuclear fuel (SNF) criticality safety evaluations based on best-available data and methods and (2) apply the approach for representative SNF storage and transport configurations/conditions to demonstrate its usage and applicability, as well as to provide reference bias results. The purpose of this paper is to describe the criticality (k{sub eff}) validation approach, and resulting observations and recommendations. Validation of the isotopic composition (depletion) calculations is addressed in a companion paper at this conference. For criticality validation, the approach is to utilize (1) available laboratory critical experiment (LCE) data from the International Handbook of Evaluated Criticality Safety Benchmark Experiments and the French Haut Taux de Combustion (HTC) program to support validation of the principal actinides and (2) calculated sensitivities, nuclear data uncertainties, and the limited available fission

  18. Delayed Fission Product Gamma-Ray Transmission Through Low Enriched UO2 Fuel Pin Lattices in Air

    SciTech Connect

    Trumbull, TH

    2004-10-18

    The transmission of delayed fission-product gamma rays through various arrangements of low-enriched UO2 fuel pin lattices in an air medium was studied. Experimental measurements, point-kernel and Monte Carlo photon transport calculations were performed to demonstrate the shielding effect of ordered lattices of fuel pins on the resulting gamma-ray dose to a detector outside the lattice. The variation of the gamma-ray dose on the outside of the lattice as a function of radial position, the so-called “channeling” effect, was analyzed. Techniques for performing experimental measurements and data reduction at Rensselaer Polytechnic Institute’s Reactor Critical Facility (RCF) were derived. An experimental apparatus was constructed to hold the arrangements of fuel pins for the measurements. A gamma-ray spectroscopy system consisting of a sodium-iodide scintillation detector was used to collect data. Measurements were made with and without a collimator installed. A point-kernel transport code was developed to map the radial dependence of the gamma-ray flux. Input files for the Monte Carlo code, MCNP, were also developed to accurately model the experimental measurements. The results of the calculations were compared to the experimental measurements. In order to determine the delayed fission-product gamma-ray source for the calculations, a technique was developed using a previously written code, DELBG and the reactor state-point data obtained during the experimental measurements. Calculations were performed demonstrating the effects of material homogenization on the gamma-ray transmission through the fuel pin lattice.Homogeneous and heterogeneous calculations were performed for all RCF fuel pin lattices as well as for a typical commercial pressurized water reactor fuel bundle. The results of the study demonstrated the effectiveness of the experimental measurements to isolate the channeling effect of delayed fission-product gamma-rays through lattices of RCF fuel pins

  19. Energy Dependence of Fission Product Yields from 235U, 238U and 239Pu for Incident Neutron Energies Between 0.5 and 14.8 MeV

    NASA Astrophysics Data System (ADS)

    Gooden, M.; Arnold, C.; Bredeweg, T.; Vieira, D.; Wilhelmy, J.; Tonchev, A.; Stoyer, M.; Bhike, M.; Krishichayan, F.; Tornow, W.; Fowler, M.

    2015-10-01

    Under a joint collaboration between TUNL-LANL-LLNL, a set of absolute fission product yield measurements has been performed. The energy dependence of a number of cumulative fission product yields (FPY) have been measured using quasi-monoenergetic neutron beams for three actinide targets, 235U, 238U and 239Pu, between 0.5 and 14.8 MeV. The FPYs were measured by a combination of fission counting using specially designed dual-fission chambers and ?-ray counting. Each dual-fission chamber is a back-to-back ionization chamber encasing an activation target in the center with thin deposits of the same target isotope in each chamber. This method allows for the direct measurement of the total number of fissions in the activation target with no reference to the fission cross-section, thus reducing uncertainties. ?-ray counting of the activation target was performed on well-shielded HPGe detectors over a period of 2 months post irradiation to properly identify fission products. Reported are absolute cumulative fission product yields for incident neutron energies of 0.5, 1.37, 2.4, 3.6, 4.6, 5.5, 7.5, 8.9 and 14.8 MeV. These results are compared to previous measurements and theoretical estimates. This work was performed under the auspices of the USDoE by Los Alamos National Security, LLC under Contract DE-AC52-06NA25396.

  20. Deep Atomic Binding (DAB) Hypothesis: A New Approach of Fission Product Chemistry

    SciTech Connect

    Ajlouni, Abdul-Wali M.S.

    2006-07-01

    Former studies assumed that, after fission process occurs, the highly ionized new born atoms (20-22 positive charge), ionize the media in which they pass through before becoming stable atoms in a manner similar to 4-MeV ?-particles. Via ordinary chemical reactions with the surroundings, each stable atom has a probability to form chemical compound. Since there are about 35 different elemental atoms created through fission processes, a large number of chemical species were suggested to be formed. But, these suggested chemical species were not found in the environment after actual releases of FP during accidents like TMI (USA, 1979), and Chernobyl (former USSR, 1986), also the models based on these suggested reactions and species could not interpret the behavior of these actual species. It is assumed here that the ionization states of the new born atoms and the long term high temperature were not dealt with in an appropriate way and they were the reasons of former models failure. Our new approach of Deep Atomic Binding (DAB) based on the following: 1-The new born atoms which are highly ionized, 10-12 electrons associated with each nucleus, having a large probability to create bonds between them to form molecules. These bonds are at the L, or M shells, and we call it DAB. 2-The molecules stay in the reactor at high temperatures for long periods, so they undergo many stages of composition and decomposition to form giant molecules. By applying DAB approach, field data from Chernobyl, TMI and nuclear detonations could be interpreted with a wide coincidence resulted. (author)

  1. On-line fission products measurements during a PWR severe accident: the French DECA-PF project

    SciTech Connect

    Ducros, G.; Allinei, P.G.; Roure, C.; Rozel, C.; Blanc De Lanaute, N.; Musoyan, G.

    2015-07-01

    Following the Fukushima accident, a lot of recommendations was drawn by international organizations (IAEA, OECD, NUGENIA network...) in order to improve the safety in such accidental conditions and mitigate their consequences. One of these recommendations was to improve the robustness of the instrumentation, which was dramatically lacking at Fukushima, as well as to better determine the Source Term involved in nuclear accident. The DECA-PF project (Diagnosis of a degraded reactor core through Fission Product measurements) was elaborated in this context and selected as one of 21 collaborative R and D projects in the field of nuclear safety and radioprotection, funded in May 2013 by the French National Research Agency. Over the months following the Fukushima accident, a CEA crisis team was held in order to analyze on-line the situation taking into account the data delivered by TEPCO and other organizations. Despite the difficulties encountered concerning the reliability of these data, the work performed showed the high capacity of Fission Products (FP) measurements to get a diagnosis relative to the status of the reactors and the spent fuel pools (SFP). Based on these FP measurements, it was possible to conclude that the main origin of the releases was coming from the cores and not from the SFP, in particular for SFP-4 which was of high concern, and that the degradation level of the reactors was very large, including probably an extensive core melting. To improve the reliability of this kind of diagnosis, the necessity to get such measurements as soon as possible after the accident and as near as possible from the reactor was stressed. In this way the present DECA-PF project intends to develop a new and innovative instrumentation taking into account the design of the French nuclear power plants on which sand bed filters have been implemented for severe accident management. Three complementary techniques, devoted to measure the FP release on-line, are being studied

  2. Molecular Dynamics Simulation of Thermal Transport in UO2 Containing Uranium, Oxygen, and Fission-product Defects

    NASA Astrophysics Data System (ADS)

    Liu, X.-Y.; Cooper, M. W. D.; McClellan, K. J.; Lashley, J. C.; Byler, D. D.; Bell, B. D. C.; Grimes, R. W.; Stanek, C. R.; Andersson, D. A.

    2016-10-01

    Uranium dioxide (UO2 ) is the most commonly used fuel in light-water nuclear reactors and thermal conductivity controls the removal of heat produced by fission, thereby governing fuel temperature during normal and accident conditions. The use of fuel performance codes by the industry to predict operational behavior is widespread. A primary source of uncertainty in these codes is thermal conductivity, and optimized fuel utilization may be possible if existing empirical models are replaced with models that incorporate explicit thermal-conductivity-degradation mechanisms during fuel burn up. This approach is able to represent the degradation of thermal conductivity due to each individual defect type, rather than the overall burn-up measure typically used, which is not an accurate representation of the chemical or microstructure state of the fuel that actually governs thermal conductivity and other properties. To generate a mechanistic thermal conductivity model, molecular dynamics (MD) simulations of UO2 thermal conductivity including representative uranium and oxygen defects and fission products are carried out. These calculations employ a standard Buckingham-type interatomic potential and a potential that combines the many-body embedded-atom-method potential with Morse-Buckingham pair potentials. Potential parameters for UO2 +x and ZrO2 are developed for the latter potential. Physical insights from the resonant phonon-spin-scattering mechanism due to spins on the magnetic uranium ions are introduced into the treatment of the MD results, with the corresponding relaxation time derived from existing experimental data. High defect scattering is predicted for Xe atoms compared to that of La and Zr ions. Uranium defects reduce the thermal conductivity more than oxygen defects. For each defect and fission product, scattering parameters are derived for application in both a Callaway model and the corresponding high-temperature model typically used in fuel-performance codes

  3. Molecular dynamics simulation of thermal transport in UO2 containing uranium, oxygen, and fission-product defects

    DOE PAGES

    Liu, Xiang -Yang; Cooper, Michael William D.; McClellan, Kenneth James; ...

    2016-10-25

    Uranium dioxide (UO2) is the most commonly used fuel in light-water nuclear reactors and thermal conductivity controls the removal of heat produced by fission, thereby governing fuel temperature during normal and accident conditions. The use of fuel performance codes by the industry to predict operational behavior is widespread. A primary source of uncertainty in these codes is thermal conductivity, and optimized fuel utilization may be possible if existing empirical models are replaced with models that incorporate explicit thermal-conductivity-degradation mechanisms during fuel burn up. This approach is able to represent the degradation of thermal conductivity due to each individual defect type,more » rather than the overall burn-up measure typically used, which is not an accurate representation of the chemical or microstructure state of the fuel that actually governs thermal conductivity and other properties. To generate a mechanistic thermal conductivity model, molecular dynamics (MD) simulations of UO2 thermal conductivity including representative uranium and oxygen defects and fission products are carried out. These calculations employ a standard Buckingham-type interatomic potential and a potential that combines the many-body embedded-atom-method potential with Morse-Buckingham pair potentials. Potential parameters for UO2+x and ZrO2 are developed for the latter potential. Physical insights from the resonant phonon-spin-scattering mechanism due to spins on the magnetic uranium ions are introduced into the treatment of the MD results, with the corresponding relaxation time derived from existing experimental data. High defect scattering is predicted for Xe atoms compared to that of La and Zr ions. Uranium defects reduce the thermal conductivity more than oxygen defects. For each defect and fission product, scattering parameters are derived for application in both a Callaway model and the corresponding high-temperature model typically used in fuel

  4. Collection of fission and activation product elements from fresh and ocean waters: a comparison of traditional and novel sorbents

    SciTech Connect

    Johnson, Bryce E.; Santschi, Peter H.; Addleman, Raymond S.; Douglas, Matthew; Davidson, Joseph D.; Fryxell, Glen E.; Schwantes, Jon M.

    2010-04-01

    Monitoring natural waters for the inadvertent release of radioactive fission products produced as a result of nuclear power generation downstream from these facilities is essential for maintaining water quality. To this end, we evaluated sorbents for simultaneous in-situ large volume extraction of radionuclides with both soft (e.g., Ag) and hard metal (e.g., Co, Zr, Nb, Ba, and Cs) or anionic (e.g., Ru, Te, Sb) character. In this study, we evaluated a number of conventional and novel nanoporous sorbents in both fresh and salt waters. In most cases, the nanoporous sorbents demonstrated enhanced retention of analytes. Salinity had significant effects upon sorbent performance and was most significant for hard cations, specifically Cs and Ba. The presence of natural organic matter had little effect on the ability of chemisorbents to extract target elements.

  5. A separate effect study of the influence of metallic fission products on CsI radioactive release from nuclear fuel

    NASA Astrophysics Data System (ADS)

    Di Lemma, F. G.; Colle, J. Y.; Beneš, O.; Konings, R. J. M.

    2015-10-01

    The chemistry of cesium and iodine is of main importance to quantify the radioactive release in case of a nuclear reactor accident, or sabotage involving irradiated nuclear materials. We studied the interaction of CsI with different metallic fission products such as Mo and Ru. These elements can be released from nuclear fuel when exposed to oxidising conditions, as in the case of contact of overheated nuclear fuel with air (e.g. in a spent fuel cask sabotage, uncovering of a spent fuel pond, or air ingress accidents). Experiments were performed by vaporizing mixtures of the compounds in air, and analysing the produced aerosols in view of a possible gas-gas and gas-aerosol reactions between the compounds. These results were compared with the gaseous species predicted by thermochemical equilibrium calculations and experimental equilibrium vaporization tests using Knudsen Effusion Mass Spectrometry.

  6. Thermal transport in UO2 with defects and fission products by molecular dynamics simulations

    SciTech Connect

    Liu, Xiang-Yang; Cooper, Michael William Donald; Mcclellan, Kenneth James; Lashley, Jason Charles; Byler, Darrin David; Stanek, Christopher Richard; Andersson, Anders David Ragnar

    2015-10-14

    The importance of the thermal transport in nuclear fuel has motivated a wide range of experimental and modelling studies. In this report, the reduction of thermal transport in UO2 due to defects and fission products has been investigated using non-equilibrium MD simulations, with two sets of empirical potentials for studying the degregation of UO2 thermal conductivity including a Buckingham type interatomic potential and a recently developed EAM type interatomic potential. Additional parameters for U5+ and Zr4+ in UO2 have been developed for the EAM potential. The thermal conductivity results from MD simulations are then corrected for the spin-phonon scattering through Callaway model formulations. To validate the modelling results, comparison was made with experimental measurements on single crystal hyper-stoichiometric UO2+x samples.

  7. A novel monolithic LEU foil target based on a PVD manufacturing process for (99)Mo production via fission.

    PubMed

    Hollmer, Tobias; Petry, Winfried

    2016-12-01

    (99)Mo is the most widely used radioactive isotope in nuclear medicine. Its main production route is the fission of uranium. A major challenge for a reliable supply is the conversion from highly enriched uranium (HEU) to low enriched uranium (LEU). A promising candidate to realize this conversion is the cylindrical LEU irradiation target. The target consists of a uranium foil encapsulated between two coaxial aluminum cladding cylinders. This target allows a separate processing of the irradiated uranium foil and the cladding when recovering the (99)Mo. Thereby, both the costs and the volume of highly radioactive liquid waste are significantly reduced compared to conventional targets. The presented manufacturing process is based on the direct coating of the uranium on the inside of the outer cladding cylinder. This process was realized by a cylindrical magnetron enhanced physical vapor deposition (PVD) technique. The method features a highly automated process, a good quality of the resulting uranium foils and a high material utilization.

  8. Fission-product yield data from the US/UK joint experiment in the Dounreay Prototype Fast Reactor

    SciTech Connect

    Dickens, J.K.; Raman, S.

    1986-04-01

    The United States and the United Kingdom have been engaged in a joint research program in which samples of fissile and fertile actinides have been incorporated in fuel pins and irradiated in the Dounreay Prototype Fast Reactor in Scotland. The purpose of this portion of the program is to study both the materials behavior and the nuclear physics results - primarily measurements of the fission-product yields in the irradiated samples and secondarily information on the amounts of heavy elements in the samples. In the measurements high-resolution detectors were used to observe and (quantitatively measure) the gamma rays and x rays corresponding to the decay of several long-lived radioisotopes. Two series of measurements were made, one nine months following the end of the irradiation period and another approximately six months later.

  9. Determination of critical assembly absolute power using post-irradiation activation measurement of week-lived fission products.

    PubMed

    Košťál, Michal; Švadlenková, Marie; Milčák, Ján; Rypar, Vojtěch; Koleška, Michal

    2014-07-01

    The work presents a detailed comparison of calculated and experimentally determined net peak areas of longer-living fission products after 100 h irradiation on a reactor with power of ~630 W and several days cooling. Specifically the nuclides studied are (140)Ba, (103)Ru, (131)I, (141)Ce, (95)Zr. The good agreement between the calculated and measured net peak areas, which is better than in determination using short lived (92)Sr, is reported. The experiment was conducted on the VVER-1000 mock-up installed on the LR-0 reactor. The Monte Carlo approach has been used for calculations. The influence of different data libraries on results of calculation is discussed as well. Copyright © 2014 Elsevier Ltd. All rights reserved.

  10. Collection of fission and activation product elements from fresh and ocean waters: a comparison of traditional and novel sorbents.

    PubMed

    Johnson, Bryce E; Santschi, Peter H; Addleman, Raymond Shane; Douglas, Matt; Davidson, Joseph D; Fryxell, Glen E; Schwantes, Jon M

    2011-01-01

    Monitoring natural waters for the inadvertent release of radioactive fission products produced as a result of nuclear power generation downstream from these facilities is essential for maintaining water quality. To this end, we evaluated sorbents for simultaneous in-situ large volume extraction of radionuclides with both soft (e.g., Ag) and hard metal (e.g., Co, Zr, Nb, Ba, and Cs) or anionic (e.g., Ru, Te, Sb) character. In this study, we evaluated a number of conventional and novel nanoporous sorbents in both fresh and salt waters. In most cases, the nanoporous sorbents demonstrated enhanced retention of analytes. Salinity had significant effects upon sorbent performance and was most significant for hard cations, specifically Cs and Ba. The presence of natural organic matter had little effect on the ability of chemisorbents to extract target elements. Copyright © 2010. Published by Elsevier Ltd.

  11. Arrival time and magnitude of airborne fission products from the Fukushima, Japan, reactor incident as measured in Seattle, WA, USA.

    PubMed

    Leon, J Diaz; Jaffe, D A; Kaspar, J; Knecht, A; Miller, M L; Robertson, R G H; Schubert, A G

    2011-11-01

    We report results of air monitoring started due to the recent natural catastrophe on 11 March 2011 in Japan and the severe ensuing damage to the Fukushima Dai-ichi nuclear reactor complex. On 17-18 March 2011, we registered the first arrival of the airborne fission products (131)I, (132)I, (132)Te, (134)Cs, and (137)Cs in Seattle, WA, USA, by identifying their characteristic gamma rays using a germanium detector. We measured the evolution of the activities over a period of 23 days at the end of which the activities had mostly fallen below our detection limit. The highest detected activity from radionuclides attached to particulate matter amounted to 4.4 ± 1.3 mBq m(-3) of (131)I on 19-20 March.

  12. Computational Benchmark for Estimation of Reactivity Margin from Fission Products and Minor Actinides in PWR Burnup Credit

    SciTech Connect

    Wagner, J.C.

    2001-08-02

    This report proposes and documents a computational benchmark problem for the estimation of the additional reactivity margin available in spent nuclear fuel (SNF) from fission products and minor actinides in a burnup-credit storage/transport environment, relative to SNF compositions containing only the major actinides. The benchmark problem/configuration is a generic burnup credit cask designed to hold 32 pressurized water reactor (PWR) assemblies. The purpose of this computational benchmark is to provide a reference configuration for the estimation of the additional reactivity margin, which is encouraged in the U.S. Nuclear Regulatory Commission (NRC) guidance for partial burnup credit (ISG8), and document reference estimations of the additional reactivity margin as a function of initial enrichment, burnup, and cooling time. Consequently, the geometry and material specifications are provided in sufficient detail to enable independent evaluations. Estimates of additional reactivity margin for this reference configuration may be compared to those of similar burnup-credit casks to provide an indication of the validity of design-specific estimates of fission-product margin. The reference solutions were generated with the SAS2H-depletion and CSAS25-criticality sequences of the SCALE 4.4a package. Although the SAS2H and CSAS25 sequences have been extensively validated elsewhere, the reference solutions are not directly or indirectly based on experimental results. Consequently, this computational benchmark cannot be used to satisfy the ANS 8.1 requirements for validation of calculational methods and is not intended to be used to establish biases for burnup credit analyses.

  13. I-NERI ANNUAL TECHNICAL PROGRESS REPORT: 2006-002-K, Separation of Fission Products from Molten LiCl-KCl Salt Used for Electrorefining of Metal Fuels

    SciTech Connect

    S. Frank

    2009-09-01

    An attractive alternative to the once-through disposal of electrorefiner salt is to selectively remove the active fission products from the salt and recycle the salt back to the electrorefiner (ER). This would allow salt reuse for some number of cycles before ultimate disposal of the salt in a ceramic waste form. Reuse of ER salt would, thus, greatly reduce the volume of ceramic waste produced during the pyroprocessing of spent nuclear fuel. This final portion of the joint I-NERI research project is to demonstrate the separation of fission products from molten ER salt by two methods previously selected during phase two (FY-08) of this project. The two methods selected were salt/zeolite contacting and rare-earth fission product precipitation by oxygen bubbling. The ER salt used in these tests came from the Mark-IV electrorefiner used to anodically dissolved driver fuel from the EBR-II reactor on the INL site. The tests were performed using the Hot Fuel Dissolution Apparatus (HFDA) located in the main cell of the Hot Fuels Examination Facility (HFEF) at the Materials and Fuels complex on the INL site. Results from these tests were evaluated during a joint meeting of KAERI and INL investigators to provide recommendations as to the future direction of fission product removal from electrorefiner salt that accumulate during spent fuel treatment. Additionally, work continued on kinetic measurements of surrogate quaternary salt systems to provide fundamental kinetics on the ion exchange system and to expand the equilibrium model system developed during the first two phases of this project. The specific objectives of the FY09 I-NERI research activities at the INL include the following: • Perform demonstration tests of the selected KAERI precipitation and INL salt/zeolite contacting processes for fission product removal using radioactive, fission product loaded ER salt • Continue kinetic studies of the quaternary Cs/Sr-LiCl-KCl system to determine the rate of ion

  14. State-of-the-art on instant release of fission products from spent nuclear fuel

    SciTech Connect

    Kienzler, Bernhard; Gonzalez-Robles, Ernesto

    2013-07-01

    Within the EURATOM FP7 Collaborative Project 'Fast / Instant Release of Safety Relevant Radionuclides from Spent Nuclear Fuel (CP FIRST-Nuclides)', a State-of-the-Art Report was prepared. The fast / instant release fraction (IRF) is defined as a fraction of the inventory of radionuclides that may be rapidly released from the fuel and fuel assembly materials at the time of canister breaching. In the context of safety analysis for a repository, the time span for mobilization of this fraction can be considered instantaneously, even if the process takes some time in experiments. Radionuclides contributing to the fast release are fission gases (Kr and Xe), easily soluble elements such as cesium and iodine, and other elements which are hardly incorporated in the UO{sub 2} crystal lattice. The present contribution summarizes the results obtained from published studies focused on rapid release experiments carried out with different spent nuclear fuel (SNF), samples, sizes, techniques (batch and flow-through), and durations. A total of 80 experiments cover the study of UO{sub 2} SNF from pressure water reactors (PWR) of different initial enrichments and burn-up, while 20 experiments were performed with UO{sub 2} SNF from boiling water reactors (BWR) and 8 with MOX fuel. (authors)

  15. Mobile neutron/gamma waste assay system for characterization of waste containing transuranics, uranium, and fission/activation products

    SciTech Connect

    Davidson, D.R.; Haggard, D.; Lemons, C.

    1994-12-31

    A new integrated neutron/gamma assay system has been built for measuring 55-gallon drums at Pacific Northwest Laboratory. The system is unique because it allows simultaneous measurement of neutrons and gamma-rays. This technique also allows measurement of transuranics (TRU), uranium, and fission/activation products, screening for shielded Special Nuclear Material prior to disposal, and critically determinations prior to transportation. The new system is positioned on a platform with rollers and installed inside a trailer or large van to allow transportation of the system to the waste site instead of movement of the drums to the scanner. The ability to move the system to the waste drums is particularly useful for drum retrieval programs common to all DOE sites and minimizes transportation problems on the site. For longer campaigns, the system can be moved into a facility. The mobile system consists of two separate subsystems: a passive Segmented Gamma Scanner (SGS) and a {open_quotes}clam-shell{close_quotes} passive neutron counter. The SGS with high purity germanium detector and {sup 75}Se transmission source simultaneously scan the height of the drum allowing identification of unshieled {open_quotes}hot spots{close_quotes} in the drum or segments where the matrix is too dense for the transmission source to penetrate. Dense segments can flag shielding material that could be used to hide plutonium or uranium during the gamma analysis. The passive nuetron counter with JSR-12N Neutron Coincidence Analyzer measures the coincident neutrons from the spontaneous fission of even isotopes of plutonium. Because high-density shielding produces minimal absorption of neutrons, compared to gamma rays, the passive neutron portion of the system can detect shielded SNM. Measurements to evaluate the performance of the system are still underway at Pacific Northwest Laboratory.

  16. Modernizing the Fission Basis

    NASA Astrophysics Data System (ADS)

    Tonchev, Anton; Henderson, Roger; Schunck, Nicolas; Sroyer, Mark; Vogt, Ramona

    2016-09-01

    In 1939, Niels Bohr and John Wheeler formulated a theory of neutron-induced nuclear fission based on the hypothesis of the compound nucleus. Their theory, the so-called ``Bohr hypothesis,'' is still at the heart of every theoretical fission model today and states that the decay of a compound nucleus for a given excitation energy, spin, and parity is independent of its formation. We propose the first experiment to validate to 1-2% absolute uncertainties the practical consequences of the Bohr hypothesis during induced nuclear fission. We will compare the fission product yields (FPYs) of the same 240Pu compound nucleus produced via two different reactions (i) n+239Pu and (ii) γ+240 Pu. These high-precision FPYs measurements will be extremely beneficial for our fundamental understanding of the nuclear fission process and nuclear reactions from first principles. This work was performed under the auspices of US DOE by LLNL under Contract DE-AC52-07NA27344. Funding was provided via the LDRD-ERD-069 project.

  17. Benchmarking nuclear fission theory

    DOE PAGES

    Bertsch, G. F.; Loveland, W.; Nazarewicz, W.; ...

    2015-05-14

    We suggest a small set of fission observables to be used as test cases for validation of theoretical calculations. Thus, the purpose is to provide common data to facilitate the comparison of different fission theories and models. The proposed observables are chosen from fission barriers, spontaneous fission lifetimes, fission yield characteristics, and fission isomer excitation energies.

  18. Benchmarking nuclear fission theory

    SciTech Connect

    Bertsch, G. F.; Loveland, W.; Nazarewicz, W.; Talou, P.

    2015-05-14

    We suggest a small set of fission observables to be used as test cases for validation of theoretical calculations. Thus, the purpose is to provide common data to facilitate the comparison of different fission theories and models. The proposed observables are chosen from fission barriers, spontaneous fission lifetimes, fission yield characteristics, and fission isomer excitation energies.

  19. Radiochemistry and the Study of Fission

    SciTech Connect

    Rundberg, Robert S.

    2016-11-14

    These are slides from a lecture given at UC Berkeley. Radiochemistry has been used to study fission since it’ discovery. Radiochemical methods are used to determine cumulative mass yields. These measurements have led to the two-mode fission hypothesis to model the neutron energy dependence of fission product yields. Fission product yields can be used for the nuclear forensics of nuclear explosions. The mass yield curve depends on both the fuel and the neutron spectrum of a device. Recent studies have shown that the nuclear structure of the compound nucleus can affect the mass yield distribution. The following topics are covered: In the beginning: the discovery of fission; forensics using fission products: what can be learned from fission products, definitions of R-values and Q-values, fission bases, K-factors and fission chambers, limitations; the neutron energy dependence of the mass yield distribution (the two mode fission hypothesis); the influence of nuclear structure on the mass yield distribution. In summary: Radiochemistry has been used to study fission since it’s discovery. Radiochemical measurement of fission product yields have provided the highest precision data for developing fission models and for nuclear forensics. The two-mode fission hypothesis provides a description of the neutron energy dependence of the mass yield curve. However, data is still rather sparse and more work is needed near second and third chance fission. Radiochemical measurements have provided evidence for the importance of nuclear states in the compound nucleus in predicting the mass yield curve in the resonance region.

  20. Production of 3-hydroxypropionic acid via the malonyl-CoA pathway using recombinant fission yeast strains.

    PubMed

    Suyama, Akiko; Higuchi, Yujiro; Urushihara, Masahiro; Maeda, Yuka; Takegawa, Kaoru

    2017-10-01

    3-Hydroxypropionic acid (3-HP) can be converted into derivatives such as acrylic acid, a source for producing super absorbent polymers. Although Escherichia coli has often been used for 3-HP production, it exhibits low tolerance to 3-HP. To circumvent this problem, we selected the fission yeast Schizosaccharomyces pombe as this microorganism has higher tolerance to 3-HP than E. coli. Therefore, we constructed S. pombe transformants overexpressing two genes, one encoding the S. pombe acetyl-CoA carboxylase (Cut6p) and the other encoding the malonyl-CoA reductase derived from Chloroflexus aurantiacus (CaMCR). To prevent the degradation of these expressed proteins, we employed an S. pombe protease-deficient strain. Moreover, to increase the cytosolic concentration of acetyl-CoA, we supplemented acetate to the medium, which improved 3-HP production. To further produce 3-HP by overexpressing Cut6p and CaMCR, we exploited the highly expressing S. pombe hsp9 promoter. Finally, culturing in high-density reached 3-HP production to 7.6 g/L at 31 h. Copyright © 2017 The Society for Biotechnology, Japan. Published by Elsevier B.V. All rights reserved.

  1. Ionizing radiation accelerates Drp1-dependent mitochondrial fission, which involves delayed mitochondrial reactive oxygen species production in normal human fibroblast-like cells

    SciTech Connect

    Kobashigawa, Shinko; Suzuki, Keiji; Yamashita, Shunichi

    2011-11-04

    Highlights: Black-Right-Pointing-Pointer We report first time that ionizing radiation induces mitochondrial dynamic changes. Black-Right-Pointing-Pointer Radiation-induced mitochondrial fission was caused by Drp1 localization. Black-Right-Pointing-Pointer We found that radiation causes delayed ROS from mitochondria. Black-Right-Pointing-Pointer Down regulation of Drp1 rescued mitochondrial dysfunction after radiation exposure. -- Abstract: Ionizing radiation is known to increase intracellular level of reactive oxygen species (ROS) through mitochondrial dysfunction. Although it has been as a basis of radiation-induced genetic instability, the mechanism involving mitochondrial dysfunction remains unclear. Here we studied the dynamics of mitochondrial structure in normal human fibroblast like cells exposed to ionizing radiation. Delayed mitochondrial O{sub 2}{sup {center_dot}-} production was peaked 3 days after irradiation, which was coupled with accelerated mitochondrial fission. We found that radiation exposure accumulated dynamin-related protein 1 (Drp1) to mitochondria. Knocking down of Drp1 expression prevented radiation induced acceleration of mitochondrial fission. Furthermore, knockdown of Drp1 significantly suppressed delayed production of mitochondrial O{sub 2}{sup {center_dot}-}. Since the loss of mitochondrial membrane potential, which was induced by radiation was prevented in cells knocking down of Drp1 expression, indicating that the excessive mitochondrial fission was involved in delayed mitochondrial dysfunction after irradiation.

  2. Influence of the incident particle energy on the fission product mass distribution.

    SciTech Connect

    Gomes, I. C.

    1998-08-26

    For {sup 238}U targets and the five elements considered here, the best yields of neutron-rich isotopes are obtained from neutrons in the 2-20 MeV range. High energy beams of neutrons, protons, and deuterons have comparable integral yields per element to neutrons below 20 MeV, but the distributions are peaked at lower neutron numbers. This is presumably due to a higher neutron multiplicity in the pre-equilibrium stage and/or the compound nucleus/fission stage. For {sup 235}U targets there are high yields predicted especially for thermal neutrons, and also for the fast neutron spectrum. For the high energy neutrons, protons, and deuterons {sup 235}U has no advantage over {sup 238}U. A detailed comparison of the relative advantages of {sup 235}U and {sup 238}U for radioactive beam applications is beyond the scope of this study and will be addressed in the future. The present work is the first step of a more detailed analysis of various possible one- and two-step target geometry calculated with the LAHET code system. It is intended to serve as a guide in choosing geometry and beams for future studies. It is desirable to extend this study to higher beam energies, e.g. 200 to 1000 MeV, but at this time there is very little data against which to benchmark the analysis. Additional data would also permit comparisons of isotope yields beyond the tails of the distributions presented here, to even more neutron rich isotopes.

  3. Fission Spectrum

    DOE R&D Accomplishments Database

    Bloch, F.; Staub, H.

    1943-08-18

    Measurements of the spectrum of the fission neutrons of 25 are described, in which the energy of the neutrons is determined from the ionization produced by individual hydrogen recoils. The slow neutrons producing fission are obtained by slowing down the fast neutrons from the Be-D reaction of the Stanford cyclotron. In order to distinguish between fission neutrons and the remaining fast cyclotron neutrons both the cyclotron current and the pusle amplifier are modulated. A hollow neutron container, in which slow neutrons have a lifetime of about 2 milliseconds, avoids the use of large distances. This method results in much higher intensities than the usual modulation arrangement. The results show a continuous distribution of neutrons with a rather wide maximum at about 0.8 MV falling off to half of its maximum value at 2.0 MV. The total number of netrons is determined by comparison with the number of fission fragments. The result seems to indicate that only about 30% of the neutrons have energies below .8 MV. Various tests are described which were performed in order to rule out modification of the spectrum by inelastic scattering. Decl. May 4, 1951

  4. Bimodal fission

    SciTech Connect

    Hulet, E.K.

    1989-04-19

    In recent years, we have measured the mass and kinetic-energy distributions from the spontaneous fission of /sup 258/Fm, /sup 259/Md, /sup 260/Md, /sup 258/No, /sup 262/No, and /sup 260/(104). All are observed to fission with a symmetrical division of mass, whereas the total-kinetic-energy (TKE) distributions strongly deviated from the Gaussian shape characteristically found in the fission of all other actinides. When the TKE distributions are resolved into two Gaussians the constituent peaks lie near 200 and near 233 MeV. We conclude two modes or bimodal fission is occurring in five of the six nuclides studied. Both modes are possible in the same nuclides, but one generally predominates. We also conclude the low-energy but mass-symmetrical mode is likely to extend to far heavier nuclei; while the high-energy mode will be restricted to a smaller region, a region of nuclei defined by the proximity of the fragments to the strong neutron and proton shells in /sup 132/Sn. 16 refs., 7 figs., 1 tab.

  5. Spallation reaction study for fission products in nuclear waste: Cross section measurements for 137Cs and 90Sr on proton and deuteron

    NASA Astrophysics Data System (ADS)

    Wang, H.; Otsu, H.; Sakurai, H.; Ahn, D. S.; Aikawa, M.; Doornenbal, P.; Fukuda, N.; Isobe, T.; Kawakami, S.; Koyama, S.; Kubo, T.; Kubono, S.; Lorusso, G.; Maeda, Y.; Makinaga, A.; Momiyama, S.; Nakano, K.; Niikura, M.; Shiga, Y.; Söderström, P.-A.; Suzuki, H.; Takeda, H.; Takeuchi, S.; Taniuchi, R.; Watanabe, Ya.; Watanabe, Yu.; Yamasaki, H.; Yoshida, K.

    2016-03-01

    We have studied spallation reactions for the fission products 137Cs and 90Sr for the purpose of nuclear waste transmutation. The spallation cross sections on the proton and deuteron were obtained in inverse kinematics for the first time using secondary beams of 137Cs and 90Sr at 185 MeV/nucleon at the RIKEN Radioactive Isotope Beam Factory. The target dependence has been investigated systematically, and the cross-section differences between the proton and deuteron are found to be larger for lighter spallation products. The experimental data are compared with the PHITS calculation, which includes cascade and evaporation processes. Our results suggest that both proton- and deuteron-induced spallation reactions are promising mechanisms for the transmutation of radioactive fission products.

  6. An Approach for Validating Actinide and Fission Product Burnup Credit Criticality Safety Analyses-Isotopic Composition Predictions

    SciTech Connect

    Radulescu, Georgeta; Gauld, Ian C; Ilas, Germina; Wagner, John C

    2011-01-01

    The expanded use of burnup credit in the United States (U.S.) for storage and transport casks, particularly in the acceptance of credit for fission products, has been constrained by the availability of experimental fission product data to support code validation. The U.S. Nuclear Regulatory Commission (NRC) staff has noted that the rationale for restricting the Interim Staff Guidance on burnup credit for storage and transportation casks (ISG-8) to actinide-only is based largely on the lack of clear, definitive experiments that can be used to estimate the bias and uncertainty for computational analyses associated with using burnup credit. To address the issues of burnup credit criticality validation, the NRC initiated a project with the Oak Ridge National Laboratory to (1) develop and establish a technically sound validation approach for commercial spent nuclear fuel (SNF) criticality safety evaluations based on best-available data and methods and (2) apply the approach for representative SNF storage and transport configurations/conditions to demonstrate its usage and applicability, as well as to provide reference bias results. The purpose of this paper is to describe the isotopic composition (depletion) validation approach and resulting observations and recommendations. Validation of the criticality calculations is addressed in a companion paper at this conference. For isotopic composition validation, the approach is to determine burnup-dependent bias and uncertainty in the effective neutron multiplication factor (keff) due to bias and uncertainty in isotopic predictions, via comparisons of isotopic composition predictions (calculated) and measured isotopic compositions from destructive radiochemical assay utilizing as much assay data as is available, and a best-estimate Monte Carlo based method. This paper (1) provides a detailed description of the burnup credit isotopic validation approach and its technical bases, (2) describes the application of the approach for

  7. Fifty years with nuclear fission

    SciTech Connect

    Behrens, J.W.; Carlson, A.D. )

    1989-01-01

    The news of the discovery of nuclear fission, by Otto Hahn and Fritz Strassmann in Germany, was brought to the United States by Niels Bohr in January 1939. Since its discovery, the United States, and the world for that matter, has never been the same. It therefore seemed appropriate to acknowledge the fifieth anniversary of its discovery by holding a topical meeting entitled, Fifty Years with Nuclear Fission,'' in the United States during the year 1989. The objective of the meeting was to bring together pioneers of the nuclear industry and other scientists and engineers to report on reminiscences of the past and on the more recent development in fission science and technology. The conference highlighted the early pioneers of the nuclear industry by dedicated a full day (April 26), consisting of two plenary sessions, at the National Academy of Sciences (NAS) in Washington, DC. More recent developments in fission science and technology in addition to historical reflections were topics for two fully days of sessions (April 27 and 28) at the main site of the NIST in Gaithersburg, Maryland. The wide range of topics covered in this Volume 1 by this topical meeting included plenary invited, and contributed sessions entitled: Preclude to the First Chain Reaction -- 1932 to 1942; Early Fission Research -- Nuclear Structure and Spontaneous Fission; 50 Years of Fission, Science, and Technology; Nuclear Reactors, Secure Energy for the Future; Reactors 1; Fission Science 1; Safeguards and Space Applications; Fission Data; Nuclear Fission -- Its Various Aspects; Theory and Experiments in Support of Theory; Reactors and Safeguards; and General Research, Instrumentation, and By-Product. The individual papers have been cataloged separately.

  8. Fifty years with nuclear fission

    SciTech Connect

    Behrens, J.W.; Carlson, A.D. )

    1989-01-01

    The news of the discovery of nucler fission, by Otto Hahn and Fritz Strassmann in Germany, was brought to the United States by Niels Bohr in January 1939. Since its discovery, the United States, and the world for that matter, has never been the same. It therefore seemed appropriate to acknowledge the fiftieth anniversary of its discovery by holding a topical meeting entitled, Fifty years with nuclear fission,'' in the United States during the year 1989. The objective of the meeting was to bring together pioneers of the nuclear industry and other scientists and engineers to report on reminiscences of the past and on the more recent developments in fission science and technology. The conference highlighted the early pioneers of the nuclear industry by dedicating a full day (April 26), consisting of two plenary sessions, at the National Academy of Sciences (NAS) in Washington, DC. More recent developments in fission science and technology in addition to historical reflections were topics for two full days of sessions (April 27 and 28) at the main sites of the NIST in Gaithersburg, Maryland. The wide range of topics covered by Volume 2 of this topical meeting included plenary invited, and contributed sessions entitled, Nuclear fission -- a prospective; reactors II; fission science II; medical and industrial applications by by-products; reactors and safeguards; general research, instrumentation, and by-products; and fission data, astrophysics, and space applications. The individual papers have been cataloged separately.

  9. Airborne fission products in the High Arctic after the Fukushima nuclear accident.

    PubMed

    Paatero, Jussi; Vira, Julius; Siitari-Kauppi, Marja; Hatakka, Juha; Holmén, Kim; Viisanen, Yrjö

    2012-12-01

    High-volume aerosol samples were collected at the Mt. Zeppelin Global Atmosphere Watch station, Ny-Ålesund, Svalbard (78°58'N, 11°53'E). The samples were analysed to find out if the radionuclide emissions from the Fukushima nuclear power plant accident in March 2011 could be detected also in the atmosphere of the High Arctic. Iodine-131 and (134)Cs and (137)Cs were observed from 25 March 2011 onwards. The maximum (131)I, (134)Cs and (137)Cs activity concentrations were 810 ± 20, 659 ± 13, and 675 ± 7 μBq/m(3), respectively. The comparison between the measured (131)I activity concentrations at Mt. Zeppelin and those calculated with the SILAM dispersion model revealed that the timing of plume movements could be rather well predicted with the model. The activity concentration levels between the measurements and the model calculations deviated. This can be due to the inaccuracies in the source term. The (134)Cs:(137)Cs activity ratio recorded in Svalbard was high compared to earlier incidents. The ratio was close to 1 which is in agreement with other studies of the Fukushima releases. This distinctive activity ratio in the Fukushima debris could be used as a tracer in Arctic radioecology studies if the activity concentrations are high enough to be detected.

  10. Investigation of the Distribution of Fission Products Silver, Palladium and Cadmium in Neutron Irradiated SIC using a Cs Corrected HRTEM

    SciTech Connect

    I. J. van Rooyen; E. Olivier; J. H Neethlin

    2014-10-01

    Electron microscopy examinations of selected coated particles from the first advanced gas reactor experiment (AGR-1) at Idaho National Laboratory (INL) provided important information on fission product distribution and chemical composition. Furthermore, recent research using STEM analysis led to the discovery of Ag at SiC grain boundaries and triple junctions. As these Ag precipitates were nano-sized, high resolution transmission electron microscopy (HRTEM) examination was used to provide more information at the atomic level. This paper describes some of the first HRTEM results obtained by examining a particle from Compact 4-1-1, which was irradiated to an average burnup of 19.26% fissions per initial metal atom (FIMA), a time average, volume-averaged temperature of 1072°C; a time average, peak temperature of 1182°C and an average fast fluence of 4.13 x 1021 n/cm2. Based on gamma analysis, it is estimated that this particle may have released as much as 10% of its available Ag-110m inventory during irradiation. The HRTEM investigation focused on Ag, Pd, Cd and U due to the interest in Ag transport mechanisms and possible correlation with Pd, Ag and U previously found. Additionally, Compact 4-1-1 contains fuel particles fabricated with a different fuel carrier gas composition and lower deposition temperatures for the SiC layer relative to the Baseline fabrication conditions, which are expected to reduce the concentration of SiC defects resulting from uranium dispersion. Pd, Ag, and Cd were found to co-exist in some of the SiC grain boundaries and triple junctions whilst U was found to be present in the micron-sized precipitates as well as separately in selected areas at grain boundaries. This study confirmed the presence of Pd both at inter- and intragranular positions; in the latter case specifically at stacking faults. Small Pd nodules were observed at a distance of about 6.5 micron from the inner PyC/SiC interface.

  11. GGA+U study of uranium mononitride: A comparison of the U-ramping and occupation matrix schemes and incorporation energies of fission products

    NASA Astrophysics Data System (ADS)

    Claisse, Antoine; Klipfel, Marco; Lindbom, Niclas; Freyss, Michel; Olsson, Pär

    2016-09-01

    Uranium mononitride is studied in the DFT + U framework. Its ground state is investigated and a study of the incorporation of diverse fission products in the crystal is conducted. The U-ramping and occupation matrix control (OMC) schemes are used to eliminate metastable states. Beyond a certain amount of introduced correlation, the OMC scheme starts to find a lower total energy. The OMC scheme is chosen for the second part of this study. Furthermore, the influence of the magnetic ordering is studied using the U-ramping method, showing that antiferromagnetic order is the most stable one when the U parameter is larger than 1.75 eV. The effect on the density of states is investigated and elastic constants are provided for comparison with other methods and experiments. The incorporation energies of fission products in different defect configurations are calculated and these energies are corrected to take into account the limited size of the supercell.

  12. Fuel and fission product behaviour in early phases of a severe accident. Part I: Experimental results of the PHEBUS FPT2 test

    NASA Astrophysics Data System (ADS)

    Barrachin, M.; Gavillet, D.; Dubourg, R.; De Bremaecker, A.

    2014-10-01

    One objective of the FPT2 test of the PHEBUS FP Program was to study the degradation of an irradiated UO2 fuel test section and the fission product behaviour under conditions of low steam flow. The results of the post-irradiation examinations (PIE) at the upper levels (823 and 900 mm) of the 1-m long test section are presented in this paper. Material interactions leading to local corium formation were identified: firstly between fuel and Zircaloy-4 cladding, notably at 823 mm, where the cladding melting temperature was reached, and secondly between fuel and stainless steel oxides. Regarding fission products, molybdenum left so-called metallic precipitates mainly composed of ruthenium. Xenon and caesium behave similarly whereas barium and molybdenum often seems to be associated in precipitates.

  13. Fission meter

    DOEpatents

    Rowland, Mark S [Alamo, CA; Snyderman, Neal J [Berkeley, CA

    2012-04-10

    A neutron detector system for discriminating fissile material from non-fissile material wherein a digital data acquisition unit collects data at high rate, and in real-time processes large volumes of data directly into information that a first responder can use to discriminate materials. The system comprises counting neutrons from the unknown source and detecting excess grouped neutrons to identify fission in the unknown source.

  14. Using tea as an artificial urine in a Canadian performance testing program for fission/activation products.

    PubMed

    Daka, Joseph N; Moodie, Gerry; DiNardo, Anthony; Kramer, Gary H

    2014-12-01

    In recent years, the National Calibration Reference Centre for Bioassay and In Vivo Monitoring (NCRC) at the Radiation Protection Bureau (RPB), Health Canada, has been conducting investigations with black tea to develop a matrix that can be used to replace urine in each of the following performance testing programs (PTP): (1) tritium, (2) carbon-14, (3) the DUAL (i.e., 3H/14C), and (4) fission/activation products (F/AP). A 1% tea solution with thimerosal, which had worked successfully for tritium, carbon-14, and the DUAL, was selected and tested for the F/AP PTP because of its similarity to urine in color and UV-VIS spectra. However, application of this tea to samples of the F/AP program containing 133Ba, 137Cs, 57Co, and 60Co produced precipitates, which was an unexpected result. Further experiments showed that replacement of thimerosal with an alcohol at about 5% eliminated the precipitation problem. The alcohol can be ethanol, methanol, or isopropanol. In the experiments, the 1% tea, preserved with alcohol, remained clear and stable for at least 100 d. The duration of each PTP for the NCRC is limited to 90 d. Application of the CNSC S-106 regulatory standard to the tea produced acceptable accuracy and precision results. It was concluded that a suitable tea matrix for the F/AP program had been found.

  15. Neutronic Analysis for Transmutation of Minor Actinides and Long-Lived Fission Products in a Fusion-Driven Transmuter (FDT)

    NASA Astrophysics Data System (ADS)

    Yapıcı, Hüseyin; Demir, Nesrin; Genç, Gamze

    2006-12-01

    This study presents the transmutations of both the minor actinides (MAs: 237Np, 241Am, 243Am and 244Cm) and the long-lived fission products (LLFPs: 99Tc, 129I and 135Cs), discharged from high burn-up PWR-MOX spent fuel, in a fusion-driven transmuter (FDT) and the effects of the MA and LLFP volume fractions on their transmutations. The blanket configuration of the FDT is improved by analyzing various sample blanket design combinations with different radial thicknesses. Two different transmutation zones (TZMA and TZFP which contain the MA and LLFP nuclides, respectively) are located separately from each other. The volume fractions of the MA and the LLFP are raised from 10 to 20% stepped by 2% and from 10 to 80% stepped by 5%, respectively. The calculations are performed to estimate neutronic parameters and transmutation characteristics per D-T fusion neutron. The conversion ratios (CRs) for the whole of all MAs are about 65-70%. The transmutation rates of the LLFP nuclides increase linearly with the increase of volume fractions of the MA, and the 99Tc nuclide among them has the highest transmutation rate. The variations of their transmutation rate per unit volume in the radial direction are quasi-concave parabolic.

  16. Advances in Development of the Fission Product Extraction Process for the Separation of Cesium and Strontium from Spent Nuclear Fuel

    SciTech Connect

    JAck D. Law

    2007-09-01

    The Fission Product Extraction (FPEX) Process is being developed as part of the United States Department of Energy Advanced Fuel Cycle Initiative for the simultaneous separation of cesium (Cs) and strontium (Sr) from spent light water reactor (LWR) fuel. Separation of the Cs and Sr will reduce the short-term heat load in a geological repository, and when combined with the separation of americium (Am) and curium (Cm), could increase the capacity of the geological repository by a factor of approximately 100. The FPEX process is based on two highly specific extractants: 4,4',(5')-Di-(t-butyldicyclo-hexano)-18-crown-6 (DtBuCH18C6) and Calix[4]arene-bis-(tert-octylbenzo-crown-6) (BOBCalixC6). The DtBuCH18C6 extractant is selective for strontium and the BOBCalixC6 extractant is selective for cesium. Results of flowsheet testing of the FPEX process with a simulated feed solution in 3.3-cm centrifugal contactors are detailed. Removal efficiencies, distribution coefficient data, coextraction of metals, and process hydrodynamic performance are discussed along with recommendations for future flowsheet testing with actual spent nuclear fuel.

  17. Total absorption spectroscopy study of the beta decay of fission products for reactor anti-neutrino energy spectra calculation

    NASA Astrophysics Data System (ADS)

    Fijalkowska, Aleksandra; MTAS Collaboration

    2016-09-01

    Thanks to its high efficiency for the detection of gamma-radiation, total absorption spectroscopy is an ideal technique to establish the true beta-decay feeding. The knowledge of the decay scheme is used to determine the distribution of anti-neutrino energy released in the decay. The anti-neutrino energy spectrum is used to calculate the total anti-neutrino flux emitted by reactor cores and the number of reactor anti-neutrino interactions with the detector matter. The number of measured anti-neutrino interactions with detector matter is about 6% smaller than the expected number of events. The measurements of beta decay of fission products by means of total absorption technique allow to verify expected number of anti-neutrino interactions with matter. In this contribution we would like to present the results of total absorption measurement of the beta decay of 86Br, 89Rb, 89Kr, 90gsRb, 90mRb, 90Kr and 139Xe, nuclei abundantly produced in the reactor core. The results and their impact on the anti-neutrino spectra reconstruction will be presented and discussed. This work was supported by the Office of Nuclear Physics, U. S. Department of Energy under Contracts DE-AC05-00OR22725 and by the Polish National Science Center under Contracts UMO2013/08/T/ST2/00624.

  18. Microscopic description of complex nuclear decay: Multimodal fission

    NASA Astrophysics Data System (ADS)

    Staszczak, A.; Baran, A.; Dobaczewski, J.; Nazarewicz, W.

    2009-07-01

    Our understanding of nuclear fission, a fundamental nuclear decay, is still incomplete due to the complexity of the process. In this paper, we describe a study of spontaneous fission using the symmetry-unrestricted nuclear density functional theory. Our results show that the observed bimodal fission can be explained in terms of pathways in multidimensional collective space corresponding to different geometries of fission products. We also predict a new phenomenon of trimodal spontaneous fission for some rutherfordium, seaborgium, and hassium isotopes.

  19. Microscopic description of complex nuclear decay: Multimodal fission

    SciTech Connect

    Staszczak, A.; Baran, A.; Dobaczewski, J.; Nazarewicz, W.

    2009-07-15

    Our understanding of nuclear fission, a fundamental nuclear decay, is still incomplete due to the complexity of the process. In this paper, we describe a study of spontaneous fission using the symmetry-unrestricted nuclear density functional theory. Our results show that the observed bimodal fission can be explained in terms of pathways in multidimensional collective space corresponding to different geometries of fission products. We also predict a new phenomenon of trimodal spontaneous fission for some rutherfordium, seaborgium, and hassium isotopes.

  20. Mercury emission to atmosphere from primary Zn production in China.

    PubMed

    Li, Guanghui; Feng, Xinbin; Li, Zhonggen; Qiu, Guangle; Shang, Lihai; Liang, Peng; Wang, Dingyong; Yang, Yongkui

    2010-09-15

    Emissions of mercury (Hg) to air have regional and global impacts through long range transport in the atmosphere. Primary Zn production is regarded as an important anthropogenic Hg source in China, but research on its Hg emission is limited. To gain a better understanding of Hg emissions from Zn production activities in China, field investigations at four industrial-scale Zn production plants using electrostatic process with Hg removal (HP-WR), electrostatic process without Hg removal (HP-WOR), retort Zn production (RZ), imperial smelting process (ISP), and one artisanal Zn smelting process (AZ) were carried out. In the investigation, Hg emission factors are defined as how much Hg was emitted to the atmosphere per ton Zn produced during various Zn production methods and were estimated by using mass balance method. The results showed that the estimated Hg emission factors of Zn production were 5.7+/-4.0 g Hg t(-1) Zn for HP-WR, 31+/-22 g Hg t(-1) Zn for HP-WOR, 34+/-71 g Hg t(-1) Zn for RZ, 122+/-122 g Hg t(-1) Zn g t(-1) for ISP, and 75+/-115 g Hg t(-1) Zn for AZ. Approximately 80.7-104.2 t year(-1) of Hg was emitted to atmosphere from primary Zn production during the period of 2002-2006 in China. Copyright 2010 Elsevier B.V. All rights reserved.

  1. Fission-Product Separation Based on Room-Temperature Ionic-Liquids

    SciTech Connect

    Hussey, Charles L.

    2005-06-01

    During the previous funding cycle for this project, we investigated the electrochemistry of Cs(I) in air and moisture-stable ionic liquids both with and without the addition of BOBCalixC6. These investigations revealed that the electrochemical windows of the dialkylimidazolium bis[(trifluoromethyl)sulfonyl]imide ionic liquids do not permit the direct electrochemical reduction of Cs(I), even when Hg electrodes are employed, because these organic cations are reduced at less negative potentials than Cs(I). However, Cs(I) coordinated by BOBCalixC6 can be electrolytically reduced to Cs(Hg) in tetraalkylammonium-based room-temperature ionic liquids such as tri-1-butylmethylammonium bis[(trifluoromethyl)sulfonyl]imide (Bu3MeN+Tf2N-) at Hg electrodes. Because this reduction process does not harm either the ionic liquid or the macrocycle, it is a promising method for recycling the cesium extraction system. The previous studies mentioned above were carried out under an inert atmosphere, i.e., in the absence of H2O and O2. However, it may not be economically feasible or even possible to carry out the recycling process in the absence of these contaminants during large-scale processing of aqueous tank waste. Thus, as described in our proposal, we have begun an investigation of the electrochemical recovery of Cs from the Bu3MeN+Tf2N- + BOBCalixC6 extraction system in an air atmosphere containing various amounts of water and oxygen. Our recent preliminary results were very surprising because they indicated that the electrochemical extraction process is relatively insensitive to the presence of small amounts of moisture even when the moisture content of the ionic liquid approaches 1000 ppm. Furthermore, we have found that the ''wet'' ionic liquid can be easily dehydrated under reduced pressure or by sparging with dry nitrogen gas without the need for heat or any other specialized treatment.

  2. A generalized method for characterization of 235U and 239Pu content using short-lived fission product gamma spectroscopy

    SciTech Connect

    Knowles, Justin R.; Skutnik, Steven E.; Glasgow, David C.; Kapsimalis, Roger J.

    2016-06-23

    Rapid non-destructive assay methods for trace fissile material analysis are needed in both nuclear forensics and safeguards communities. To address these needs, research at the High Flux Isotope Reactor Neutron Activation Analysis laboratory has developed a generalized non-destructive assay method to characterize materials containing fissile isotopes. This method relies on gamma-ray emissions from short-lived fission products and capitalizes off of differences in fission product yields to identify fissile compositions of trace material samples. Although prior work has explored the use of short-lived fission product gamma-ray measurements, the proposed method is the first to provide a holistic characterization of isotopic identification, mass ratios, and absolute mass determination. Successful single fissile isotope mass recoveries of less than 6% error have been conducted on standards of 235U and 239Pu as low as 12 nanograms in less than 10 minutes. Additionally, mixtures of fissile isotope standards containing 235U and 239Pu have been characterized as low as 229 nanograms of fissile mass with less than 12% error. The generalizability of this method is illustrated by evaluating different fissile isotopes, mixtures of fissile isotopes, and two different irradiation positions in the reactor. Furthermore, it is anticipated that this method will be expanded to characterize additional fissile nuclides, utilize various irradiation sources, and account for increasingly complex sample matrices.

  3. Measurements of extinct fission products in nuclear bomb debris: Determination of the yield of the Trinity nuclear test 70 y later

    SciTech Connect

    Hanson, Susan Kloek; Pollington, Anthony Douglas; Waidmann, Christopher Russell; Kinman, William Scott; Wende, Allison Marie; Miller, Jeffrey L.; Berger, Jennifer A.; Oldham, Warren James; Selby, Hugh D.

    2016-07-05

    This study describes an approach to measuring extinct fission products that would allow for the characterization of a nuclear test at any time. The isotopic composition of molybdenum in five samples of glassy debris from the 1945 Trinity nuclear test has been measured. Nonnatural molybdenum isotopic compositions were observed, reflecting an input from the decay of the short-lived fission products 95Zr and 97Zr. By measuring both the perturbation of the 95Mo/96Mo and 97Mo/96Mo isotopic ratios and the total amount of molybdenum in the Trinity nuclear debris samples, it is possible to calculate the original concentrations of the 95Zr and 97Zr isotopes formed in the nuclear detonation. Together with a determination of the amount of plutonium in the debris, these measurements of extinct fission products allow for new estimates of the efficiency and yield of the historic Trinity test.

  4. Measurements of extinct fission products in nuclear bomb debris: Determination of the yield of the Trinity nuclear test 70 y later

    SciTech Connect

    Hanson, Susan Kloek; Pollington, Anthony Douglas; Waidmann, Christopher Russell; Kinman, William Scott; Wende, Allison Marie; Miller, Jeffrey L.; Berger, Jennifer A.; Oldham, Warren James; Selby, Hugh D.

    2016-07-05

    This study describes an approach to measuring extinct fission products that would allow for the characterization of a nuclear test at any time. The isotopic composition of molybdenum in five samples of glassy debris from the 1945 Trinity nuclear test has been measured. Nonnatural molybdenum isotopic compositions were observed, reflecting an input from the decay of the short-lived fission products 95Zr and 97Zr. By measuring both the perturbation of the 95Mo/96Mo and 97Mo/96Mo isotopic ratios and the total amount of molybdenum in the Trinity nuclear debris samples, it is possible to calculate the original concentrations of the 95Zr and 97Zr isotopes formed in the nuclear detonation. Together with a determination of the amount of plutonium in the debris, these measurements of extinct fission products allow for new estimates of the efficiency and yield of the historic Trinity test.

  5. Comment on 'Propellant production from the Martian atmosphere'

    NASA Technical Reports Server (NTRS)

    Ruppe, H. O.

    1993-01-01

    The optimism of the Tauber et al. (1992) note on photosynthetic production of spacecraft fuels from Martian atmospheric gases is presently noted, in conjunction with the need for prior missions' verification of such a system. Two of the original authors reply that their solar cell array assumptions are conservative in light of plausible performance projections for 2010-decade technology.

  6. Heterogeneous production of cloud condensation nuclei in the marine atmosphere

    SciTech Connect

    Hegg, D.A. )

    1990-11-01

    Model calculations are presented which indicate that newly created particles in the marine atmosphere will commonly only be able to achieve sizes, by means of gas-phase processes, sufficient to activate a cumuliform clouds. Aqueous sulfate production in such clouds will be generally necessary to grow them large enough to activate in marine stratus clouds.

  7. METHOD OF SEPARATING FISSION PRODUCTS FROM FUSED BISMUTH-CONTAINING URANIUM

    DOEpatents

    Wiswall, R.H.

    1958-06-24

    A process is described for removing metal selectively from liquid metal compositions. The method effects separation of flssion product metals selectively from dilute solution in fused bismuth, which contains uraniunn in solution without removal of more than 1% of the uranium. The process comprises contacting the fused bismuth with a fused salt composition consisting of sodium, potassium and lithium chlorides, adding to fused bismuth and molten salt a quantity of bismuth chloride which is stoichiometrically required to convert the flssion product metals to be removed to their chlorides which are more stable in the fused salt than in the molten metal and are, therefore, preferentially taken up in the fused salt phase.

  8. DEVELOPMENT OF GLASS COMPOSITIONS TO IMMOBILIZE ALKALI, ALKALINE EARTH, LANTHANIDE AND TRANSITION METAL FISSION PRODUCTS FROM NUCLEAR FUEL REPROCESSING

    SciTech Connect

    Marra, J.; Billings, A.

    2009-06-24

    The Advanced Fuel Cycle Initiative (AFCI) waste management strategy revolves around specific treatment of individual or groups of separated waste streams. A goal for the separations processes is to efficiently manage the waste to be dispositioned as high level radioactive waste. The Advanced Fuel Cycle Initiative (AFCI) baseline technology for immobilization of the lanthanide (Ln) and transition metal fission product (TM) wastes is vitrification into a borosilicate glass. A current interest is to evaluate the feasibility of vitrifying combined waste streams to most cost effectively immobilize the wastes resulting from aqueous fuel reprocessing. Studies showed that high waste loadings are achievable for the Ln only (Option 1) stream. Waste loadings in excess of 60 wt % (on a calcined oxide basis) were demonstrated via a lanthanide borosilicate (LaBS) glass. The resulting glasses had excellent relative durability as determined by the Product Consistency Test (PCT). For a combined Ln and TM waste stream glass (Option 2), noble metal solubility was found to limit waste loading. However, the measured PCT normalized elemental releases for this glass were at least an order of magnitude below that of Environmental Assessment (EA) glass. Current efforts to evaluate the feasibility of vitrifying combined Ln, TM, alkali (Cs is the primary radionuclide of concern) and alkaline earth (Sr is the primary radionuclide of concern) wastes (Option 3) have shown that these approaches are feasible. However, waste loading limitations with respect to heat load (Cs/Sr loading), molybdenum solubility and/or noble metal solubility will likely be realized and must be considered in determining the cost effectiveness of these approaches.

  9. Coexpression of redox partners increases the hydrocortisone (cortisol) production efficiency in CYP11B1 expressing fission yeast Schizosaccharomyces pombe.

    PubMed

    Hakki, Tarek; Zearo, Silvia; Drăgan, Călin-Aurel; Bureik, Matthias; Bernhardt, Rita

    2008-02-01

    Cytochromes P450 play a vital role in the steroid biosynthesis pathway of the adrenal gland. An example of an essential P450 cytochrome is the steroid 11beta-hydroxylase CYP11B1, which catalyses the conversion of 11-deoxycorticol to hydrocortisone. However, despite its high biotechnological potential, this enzyme has so far been unsuccessfully employed in present-day biotechnology due to a poor expression yield and inherent protein instability. In this study, CYP11B1 was biotransformed into various strains of the yeast Schizosaccharomyces pombe, all of which also expressed the electron transfer proteins adrenodoxin and/or adrenodoxin reductase - central components of the mitochondrial P450 system - in order to maximise hydrocortisone production efficiency in our proposed model system. Site-directed mutagenesis of CYP11B1 at positions 52 and 78 was performed in order to evaluate the impact of altering the amino acids at these sites. It was found that the presence of an isoleucine at position 78 conferred the highest 11beta-hydroxylation activity of CYP11B1. Coexpression of adrenodoxin and adrenodoxin reductase appeared to further increase the 11beta-hydroxylase activity of the enzyme (3.4 fold). Adrenodoxin mutants which were found to significantly enhance enzyme efficiency in other cytochromes in previous studies were also tested in our system. It was found that, in this case, the wild type adrenodoxin was more efficient. The new fission yeast strain TH75 coexpressing the wild type Adx and AdR displays high hydrocortisone production efficiency at an average of 1mM hydrocortisone over a period of 72h, the highest value published to date for this biotransformation. Finally, our research shows that pTH2 is an ideal plasmid for the coexpression of the mitochondrial electron transfer counterparts, adrenodoxin and adrenodoxin reductase, in Schizosaccharomyces pombe, and so could serve as a convenient tool for future biotechnological applications.

  10. Fission product activity ratios measured at trace level over France during the Fukushima accident.

    PubMed

    de Vismes Ott, A; Gurriaran, R; Cagnat, X; Masson, O

    2013-11-01

    The nuclear accident of Fukushima Dai-ichi (Japan) which occurred after the tsunami that impacted the northeast coasts of Japan on March 11th, 2011 led to significant releases of radionuclides into the atmosphere and resulted in the detection of those radionuclides at a global scale. In order to track airborne radionuclides from the damaged reactors and to survey their potential impact on the French territory, the French Institute of Radiation Protection and Nuclear Safety (Institut de Radioprotection et de Sureté Nucléaire IRSN) set up an enhanced surveillance system to give quick results as needed and later give quality trace level measurements. Radionuclides usually measured at trace levels such as (137)Cs and in a very sporadic way (131)I were reported. Radionuclides that we had never measured in air since the Chernobyl accident: (134)Cs, (136)Cs, the mother/daughter pairs (129m)Te-(129)Te and (132)Te-(132)I, and (140)La (from the mother-daughter pair (140)Ba- (140)La) were also reported. Except the (131)I/(137)Cs ratio, activity concentration ratios were constant. These ratios could be used to help source term assessment, or as data for transfer studies realized after the passage of contaminated air masses, typically using the (134)Cs/(137)Cs ratio.

  11. Dynamical Aspects of Nuclear Fission

    NASA Astrophysics Data System (ADS)

    Kliman, J.; Itkis, M. G.; Gmuca, Š.

    2008-11-01

    Fission dynamics. Dependence of scission-neutron yield on light-fragment mass for [symbol]=1/2 [et al.]. Dynamics of capture quasifission and fusion-fission competition / L. Stuttgé ... [et al.] -- Fission-fission. The processes of fusion-fission and quasi-fission of superheavy nuclei / M. G. Itkis ... [et al.]. Fission and quasifission in the reactions [symbol]Ca+[symbol]Pb and [symbol]Ni+[symbol]W / G. N. Knyazheva ... [et al.]. Mass-energy characteristics of reactions [symbol]Fe+[symbol][symbol][symbol]266Hs and [symbol]Mg+[symbol]Cm[symbol][symbol]Hs at Coulomb barrier / L. Krupa ... [et al.]. Fusion of heavy ions at extreme sub-barrier energies / Ş. Mişicu and H. Esbensen. Fusion and fission dynamics of heavy nuclear system / V. Zagrebaev and W. Greiner. Time-dependent potential energy for fusion and fission processes / A. V. Karpov ... [et al.] -- Superheavy elements. Advances in the understanding of structure and production mechanisms for superheavy elements / W. Greiner and V. Zagrebaev. Fission barriers of heaviest nuclei / A. Sobiczewski ... [et al.]. Possibility of synthesizing doubly magic superheavy nuclei / Y Aritomo ... [et al.]. Synthesis of superheavy nuclei in [symbol]Ca-induced reactions / V. K. Utyonkov ... [et al.] -- Fragmentation. Production of neutron-rich nuclei in the nucleus-nucleus collisions around the Fermi energy / M. Veselský. Signals of enlarged core in [symbol]Al / Y. G. Ma ... [et al.] -- Exotic modes. New insight into the fission process from experiments with relativistic heavy-ion beams / K.-H. Schmidt ... [et al.]. New results for the intensity of bimodal fission in binary and ternary spontaneous fission of [symbol]Cf / C. Goodin ... [et al.]. Rare fission modes: study of multi-cluster decays of actinide nuclei / D. V. Kamanin ... [et al.]. Energy distribution of ternary [symbol]-particles in [symbol]Cf(sf) / M. Mutterer ... [et al.]. Preliminary results of experiment aimed at searching for collinear cluster tripartition of

  12. Atmospheric production of glycolaldehyde under hazy prebiotic conditions.

    PubMed

    Harman, Chester E; Kasting, James F; Wolf, Eric T

    2013-04-01

    The early Earth's atmosphere, with extremely low levels of molecular oxygen and an appreciable abiotic flux of methane, could have been a source of organic compounds necessary for prebiotic chemistry. Here, we investigate the formation of a key RNA precursor, glycolaldehyde (2-hydroxyacetaldehyde, or GA) using a 1-dimensional photochemical model. Maximum atmospheric production of GA occurs when the CH4:CO2 ratio is close to 0.02. The total atmospheric production rate of GA remains small, only 1 × 10(7) mol yr(-1). Somewhat greater amounts of GA production, up to 2 × 10(8) mol yr(-1), could have been provided by the formose reaction or by direct delivery from space. Even with these additional production mechanisms, open ocean GA concentrations would have remained at or below ~1 μM, much smaller than the 1-2 M concentrations required for prebiotic synthesis routes like those proposed by Powner et al. (Nature 459:239-242, 2009). Additional production or concentration mechanisms for GA, or alternative formation mechanisms for RNA, are needed, if this was indeed how life originated on the early Earth.

  13. Uptake of actinides and nuclear fission products in graminaceous and nongraminaceous plants

    NASA Astrophysics Data System (ADS)

    Ely, Stephanie Lynn

    Radionuclides exist within the environment naturally and also from release during nuclear power and weapons production. The ability of plants to uptake radionuclides may prove beneficial for exploitation in the field of phytoremediation and as a biomonitor within the field of nuclear forensics. The fact that plants have the ability to take up radionuclides as an unintended metabolic process is well known, however, the mechanisms through which uptake occur present large gaps within the current research. Therefore, gaining further knowledge regarding overall plant radionuclide uptake and specific mechanisms may prove as an invaluable tool to enhance phytoremediation and nuclear forensic efforts. Within this work, controlled laboratory experiments were conducted in order to determine any uptake differences between graminaceous (rye grass) and nongraminaceous (cucumber) plants. A matrix of samples were individually spiked with known amounts of Sr, Cs, Th, U as well as ligands of acetate, citrate, DFOB. Uptake was compared through the calculation and analysis of distribution coefficients within the roots and shoots of each plant sample. A variety of trends were observed throughout this study. Overall, it was determined that the cucumber plant takes up slightly higher concentrations within both the roots and the shoots, except for within the Cs set of samples. Within the Cs samples it was determined that uptake was much higher in the rye grass than in the cucumber plant. Therefore, it was concluded that it may be more beneficial to focus on the collection of grasses and other graminaceous plants when the goal is to collect a plant to determine nuclear activity within the vicinity of a facility. This is due to the fact that Cs is generally released at higher concentrations than other radionuclides during the process of nuclear power and energy production. Similarly, grasses may also be desired as the main focus for phytoremediation efforts due to the fact that Cs is a

  14. Transmutation of high-level fission products and actinides in a laser-driven fusion reactor

    SciTech Connect

    Basov, N.; Rozanov, V.B. ); Belousov, N.I.; Grishunin, P.A.; Kharitonov, V.V. ); Subbotin, V.I. )

    1992-11-01

    Incineration of [sup 90]Sr and [sup 137]Cs b thermal or fast neutrons is a very difficult problem. A 14-MeV neutron source based on intertial confinement fusion is a more appropriate choice. For the first time, the contribution of the (n,2n) reaction to incineration is revealed. The energy and nuclei balance for a system of several nuclear power plants and a fusion reactor for transmutation is analyzed. If the fusion reactor supports a sufficient number of nuclear power plants, it need not produce energy or tritium. Target and blanket material problems are considered. This paper reports that laser fusion incinerator has the best prospects because of its fast neutron spectrum and high driver efficiency by target gain product.

  15. Beta decay of the fission product 125Sb and a new complete evaluation of absolute gamma ray transition intensities

    NASA Astrophysics Data System (ADS)

    Rajput, M. U.; Ali, N.; Hussain, S.; Mujahid, S. A.; MacMahon, D.

    2012-04-01

    The radionuclide 125Sb is a long-lived fission product, which decays to 125Te by negative beta emission with a half-life of 1008 day. The beta decay is followed by the emission of several gamma radiations, ranging from low to medium energy, that can suitably be used for high-resolution detector calibrations, decay heat calculations and in many other applications. In this work, the beta decay of 125Sb has been studied in detail. The complete published experimental data of relative gamma ray intensities in the beta decay of the radionuclide 125Sb has been compiled. The consistency analysis was performed and discrepancies found at several gamma ray energies. Evaluation of the discrepant data was carried out using Normalized Residual and RAJEVAL methods. The decay scheme balance was carried out using beta branching ratios, internal conversion coefficients, populating and depopulating gamma transitions to 125Te levels. The work has resulted in the consistent conversion factor equal to 29.59(13) %, and determined a new evaluated set of the absolute gamma ray emission probabilities. The work has also shown 22.99% of the delayed intensity fraction as outgoing from the 58 d isomeric 144 keV energy level and 77.01% of the prompt intensity fraction reaching to the ground state from the other excited states. The results are discussed and compared with previous evaluations. The present work includes additional experimental data sets which were not included in the previous evaluations. A new set of recommended relative and absolute gamma ray emission probabilities is presented.

  16. Atmospheric Production of Perchlorate on Earth and Mars

    NASA Astrophysics Data System (ADS)

    Claire, M.; Catling, D. C.; Zahnle, K. J.

    2009-12-01

    Natural production and preservation of perchlorate on Earth occurs only in arid environments. Isotopic evidence suggests a strong role for atmospheric oxidation of chlorine species via pathways including ozone or its photochemical derivatives. As the Martian atmosphere is both oxidizing and drier than the driest places on Earth, we propose an atmospheric origin for the Martian perchlorates measured by NASA's Phoenix Lander. A variety of hypothetical formation pathways can be proposed including atmospheric photochemical reactions, electrostatic discharge, and gas-solid reactions. Here, we investigate gas phase formation pathways using a 1-D photochemical model (Catling et al. 2009, accepted by JGR). Because perchlorate-rich deposits in the Atacama desert are closest in abundance to perchlorate measured at NASA's Phoenix Lander site, we start with a study of the means to produce Atacama perchlorate. We found that perchlorate can be produced in sufficient quantities to explain the abundance of perchlorate in the Atacama from a proposed gas phase oxidation of chlorine volatiles to perchloric acid. These results are sensitive to estimated reaction rates for ClO3 species. The feasibility of gas phase production for the Atacama provides justification for further investigations of gas phase photochemistry as a possible source for Martian perchlorate. In addition to the Atacama results, we will present a preliminary study incorporating chlorine chemistry into an existing Martian photochemical model (Zahnle et al. JGR 2008).

  17. Future U.S. supply of Mo-99 production through fission based LEU/LEU technology.

    PubMed

    Welsh, James; Bigles, Carmen I; Valderrabano, Alejandro

    Coquí RadioPharmaceuticals Corp. (Coquí) has the goal of establishing a medical isotope production facility for securing a continuous domestic supply of the radioisotope molybdenum-99 for U.S. citizens. Coquí will use an LEU/LEU proven and implemented open pool, light-water, 10 MW, reactor design. The facility is being designed with twin reactors for reliability an on-site hot lab chemical processing and a waste conditioning area and a possible generator producing radio-chemistry lab. Coquí identified a 25 acre site adjacent to an existing industrial park in northern central Florida. This land was gifted and transferred to Coquí by the University of Florida Foundation. We are in the process of developing licensing documents related to the facility. The construction permit application for submission to the U.S. Nuclear Regulatory Commission is currently being prepared. Submission is scheduled for mid to late 2015. Community reaction to the proposed development has been positive. We expect to create 220 permanent jobs and we have an anticipated to be operational by 2020.

  18. STABILIZING GLASS BONDED WASTE FORMS CONTAINING FISSION PRODUCTS SEPARATED FROM SPENT NUCLEAR FUEL

    SciTech Connect

    Kenneth J. Bateman; Charles W. Solbrig

    2008-07-01

    A model has been developed to represent the stresses developed when a molten, glass-bonded brittle cylinder (used to store nuclear material) is cooled from high temperature to working temperature. Large diameter solid cylinders are formed by heating glass or glass-bonded mixtures (mixed with nuclear waste) to high temperature (915°C). These cylinders must be cooled as the final step in preparing them for storage. Fast cooling time is desirable for production; however, if cooling is too fast, the cylinder can crack into many pieces. To demonstrate the capability of the model, cooling rate cracking data were obtained on small diameter (7.8 cm diameter) glass-only cylinders. The model and experimental data were combined to determine the critical cooling rate which separates the non-cracking stable glass region from the cracked, non-stable glass regime. Although the data have been obtained so far only on small glass-only cylinders, the data and model were used to extrapolate the critical-cooling rates for large diameter ceramic waste form (CWF) cylinders. The extrapolation estimates long term cooling requirements. While a 52-cm diameter cylinder (EBR-II-waste size) can be cooled to 100°C in 70 hours without cracking, a 181.5-cm diameter cylinder (LWR waste size) requires 35 days to cool to 100°C. These cooling times are long enough that verification of these estimates are required so additional experiments are planned on both glass only and CWF material.

  19. Nylon production: An unknown source of atmospheric nitrous oxide

    SciTech Connect

    Thiemens, M.H.; Trogler, W.C. )

    1991-02-22

    Nitrous oxide in the earth's atmosphere contributes to catalytic stratospheric ozone destruction and is also a greenhouse gas component. A precise budgetary accounting of N{sub 2}O sources has remained elusive, and there is an apparent lack of source identification. One source of N{sub 2}O is as a by-product in the manufacture of nylon, specifically in the preparation of adipic acid. Characterization of the reaction N{sub 2}O stoichiometry and its isotopic composition with a simulated industrial adipic acid synthesis indicates that because of high rates of global adipic acid production, this N{sub 2}O may account for {approximately}10% of the increase observed for atmospheric N{sub 2}O.

  20. Compression of Martian atmosphere for production of oxygen

    NASA Technical Reports Server (NTRS)

    Lynch, D. C.; Cutler, A. H.; Nolan, P. E.

    1991-01-01

    The compression of CO2 from the Martian atmosphere for production of O2 via an electrochemical cell is addressed. Design specifications call for an oxygen production rate of 10 kg per day and for compression of 50 times that mass of CO2. Those specifications require a compression rate of over 770 cfm at standard Martian temperature and pressure (SMTP). Much of the CO2 being compressed represents waste, unless it can be recycled. Recycling can reduce the volume of gas that must be compressed to 40 cfm at SMTP. That volume reduction represents significant mass savings in the compressor, heating equipment, filters, and energy source. Successful recycle of the gas requires separation of CO (produced in the electrochemical cell) from CO2, N2, and Ar found in the Martian atmosphere. That aspect was the focus of this work.

  1. Fission-product behaviour in irradiated TRISO-coated particles: Results of the HFR-EU1bis experiment and their interpretation

    NASA Astrophysics Data System (ADS)

    Barrachin, M.; Dubourg, R.; de Groot, S.; Kissane, M. P.; Bakker, K.

    2011-08-01

    It is important to understand fission-product (FP) and kernel micro-structure evolution in TRISO-coated fuel particles. FP behaviour, while central to severe-accident evaluation, impacts: evolution of the kernel oxygen potential governing in turn carbon oxidation (amoeba effect and pressurization); particle pressurization through fission-gas release from the kernel; and coating mechanical resistance via reaction with some FPs (Pd, Cs, Sr). The HFR-Eu1bis experiment irradiated five HTR fuel pebbles containing TRISO-coated UO 2 particles and went beyond current HTR specifications (e.g., central temperature of 1523 K). This study presents ceramographic and EPMA examinations of irradiated urania kernels and coatings. Significant evolutions of the kernel (grain structure, porosity, metallic-inclusion size, intergranular bubbles) as a function of temperature are shown. Results concerning FP migration are presented, e.g., significant xenon, caesium and palladium release from the kernel, molybdenum and ruthenium mainly present in metallic precipitates. The observed FP and micro-structural evolutions are interpreted and explanations proposed. The effect of high flux rate and high temperature on fission-gas behaviour, grain-size evolution and kernel swelling is discussed. Furthermore, Cs, Mo and Zr behaviour is interpreted in connection with oxygen-potential. This paper shows that combining state-of-the-art post-irradiation examination and state-of-the-art modelling fundamentally improves understanding of HTR fuel behaviour.

  2. Photodissociation Dynamics of 2-BROMOETHYLNITRITE at 351 NM and C-C Bond Fission in the β - Radical Product

    NASA Astrophysics Data System (ADS)

    Wang, Lei; Chhantyal-Pun, Rabi; Brynteson, Matt D.; Miller, Terry A.; Butler, Laurie J.

    2013-06-01

    We used a crossed laser-molecular beam scattering experiment to investigate the primary photodissociation channels of bromoethylnitrite at 351 nm. Only the O-NO bond fission channel forming the β -bromoethoxy radical and NO, no HBr photoelimination, was detected upon 351 nm photoexcitation,. The subsequent decomposition of the highly vibrational excited β -bromoethoxy radical to formaldehyde + CH{_2}Br was also investigated.

  3. Fission dynamics within time-dependent Hartree-Fock: Deformation-induced fission

    NASA Astrophysics Data System (ADS)

    Goddard, Philip; Stevenson, Paul; Rios, Arnau

    2015-11-01

    Background: Nuclear fission is a complex large-amplitude collective decay mode in heavy nuclei. Microscopic density functional studies of fission have previously concentrated on adiabatic approaches based on constrained static calculations ignoring dynamical excitations of the fissioning nucleus and the daughter products. Purpose: We explore the ability of dynamic mean-field methods to describe fast fission processes beyond the fission barrier, using the nuclide Pu240 as an example. Methods: Time-dependent Hartree-Fock calculations based on the Skyrme interaction are used to calculate nonadiabatic fission paths, beginning from static constrained Hartree-Fock calculations. The properties of the dynamic states are interpreted in terms of the nature of their collective motion. Fission product properties are compared to data. Results: Parent nuclei constrained to begin dynamic evolution with a deformation less than the fission barrier exhibit giant-resonance-type behavior. Those beginning just beyond the barrier explore large-amplitude motion but do not fission, whereas those beginning beyond the two-fragment pathway crossing fission to final states which differ according to the exact initial deformation. Conclusions: Time-dependent Hartree-Fock is able to give a good qualitative and quantitative description of fast fission, provided one begins from a sufficiently deformed state.

  4. Long-term elevated atmospheric CO2 enhances forest productivity

    NASA Astrophysics Data System (ADS)

    Loecke, T. D.; Groffman, P. M.; Treseder, K. K.; LaDeau, S.

    2011-12-01

    that warmer sites also promote tree growth. In- growth root cores, soil N mineralization and nitrification assays, and soil C and N contents all suggest that N is unlikely to be limiting current tree productivity on most sites across our rural to urban transect. Furthermore, soil lead content varied little across these forest sites, suggesting that heavy metal contamination is not likely a significant control on forest productivity in our study. These results lend support for the overarching hypothesis that terrestrial ecosystems will sequester more C under greater atmospheric CO2 concentrations and warmer air temperatures.

  5. Fission product separations testing

    SciTech Connect

    Bostick, D.A.; DePaoli, S.M.

    1997-10-01

    The initial goal of this task is to adequately understand the treatment needs of the end user in treating contaminated wastewater. These needs are then incorporated into the evaluation of new treatment technologies for wastewater treatment. Pertinent information is than supplied to the end user so that they can select a preferred process to meet their waste treatment needs. New sorbent materials, ion-exchange materials, or other processes of interest to DOE`s Office of Environmental Restoration (EM-40) will be evaluated initially for the removal of {sup 90}Sr and {sup 137}Cs from groundwater and process wastewater. Laboratory studies will strive to obtain a quantitative understanding of the behavior of these new materials and to evaluate their sorption efficiency in reference to a standard benchmark treatment technique. Testing of the new materials will begin by conducting scoping tests where new treatment materials are compared with standard, commercially available materials in batch shaker tests. Experimental data for the most promising sorbents will then be fit to an equilibrium model so that nuclide sorption can be predicted for variable wastewater composition. Additional testing with actual wastewater will be conducted with two or three of the most effective treatment methods. Once batch testing of a treatment method is completed, dynamic column tests will be performed to validate the equilibrium sorption model and to obtain the defining column operating parameters for scaling up the technology.

  6. Does atmospheric deposition support phytoplankton productivity in Monterey Bay, CA?

    NASA Astrophysics Data System (ADS)

    Mazloom, S.; Mackey, K. R.; Paytan, A.

    2008-12-01

    Aerosol deposition has been shown to enhance phytoplankton productivity in nutrient-deplete open ocean environments, by providing phosphorus and iron to stimulate production in general and nitrogen fixation in particular. This project was designed to determine the importance of atmospheric aerosol deposition's ability to support phytoplankton in Monterey Bay, a productive upwelling region, and in waters surrounding coastal California. To conduct this experiment, MODIS satellite images of the Bay were taken from the years 2002- 2008 and were then grouped into eight day time intervals. The three factors tested in the experiment were correlations between sea surface temperature, the amount of aerosol (as determined by optical thickness), and the amount of chlorophyll. Aerosols correlated positively with chlorophyll concentrations offshore of Monterey Bay in the summer, but not within the Bay itself. No significant correlations were found for any locations in the winter months. The trends found in the experiment will be shown and the importance of atmospheric aerosol in supporting phytoplankton production in Monterey Bay will be highlighted.

  7. An Approach for Validating Actinide and Fission Product Burnup Credit Criticality Safety Analyses: Criticality (keff) Predictions

    SciTech Connect

    Scaglione, John M.; Mueller, Don E.; Wagner, John C.

    2014-12-01

    One of the most important remaining challenges associated with expanded implementation of burnup credit in the United States is the validation of depletion and criticality calculations used in the safety evaluation—in particular, the availability and use of applicable measured data to support validation, especially for fission products (FPs). Applicants and regulatory reviewers have been constrained by both a scarcity of data and a lack of clear technical basis or approach for use of the data. In this study, this paper describes a validation approach for commercial spent nuclear fuel (SNF) criticality safety (keff) evaluations based on best-available data and methods and applies the approach for representative SNF storage and transport configurations/conditions to demonstrate its usage and applicability, as well as to provide reference bias results. The criticality validation approach utilizes not only available laboratory critical experiment (LCE) data from the International Handbook of Evaluated Criticality Safety Benchmark Experiments and the French Haut Taux de Combustion program to support validation of the principal actinides but also calculated sensitivities, nuclear data uncertainties, and limited available FP LCE data to predict and verify individual biases for relevant minor actinides and FPs. The results demonstrate that (a) sufficient critical experiment data exist to adequately validate keff calculations via conventional validation approaches for the primary actinides, (b) sensitivity-based critical experiment selection is more appropriate for generating accurate application model bias and uncertainty, and (c) calculated sensitivities and nuclear data uncertainties can be used for generating conservative estimates of bias for minor actinides and FPs. Results based on the SCALE 6.1 and the ENDF/B-VII.0 cross-section libraries indicate that a conservative estimate of the bias for the minor actinides and FPs is 1.5% of their worth

  8. Gas-leaking fuel elements number and fission gas product coolant volumetric activities assessment in the VVER-440 nuclear power plant

    NASA Astrophysics Data System (ADS)

    Szuta, Marcin

    1992-07-01

    In a nuclear power plant it is required to monitor continuously the number of gas-leaking fuel elements and the contamination level of the primary coolant by fission gas products. It is proposed to use the radiation monitoring system equipped with the computer technics provided with the suitable program package for fulfilment this requirements. The input data to start up the program consists of the 88Kr volumetric activity measured by the radiation monitoring system and three actual technological parameters: coolant temperature at inlet, thermal power and coolant flow rate.

  9. A suitability study of the fission product phantom and the bottle manikin absorption phantom for calibration of in vivo bioassay equipment for the DOELAP accreditation testing program

    SciTech Connect

    Olsen, P.C.; Lynch, T.P.

    1991-08-01

    Pacific Northwest laboratory (PNL) conducted an intercomparison study of the Fission Product phantom and the bottle manikin absorption (BOMAB) phantom for the US Department of Energy (DOE) to determine the consistency of calibration response of the two phantoms and their suitability for certification and use under a planned bioassay laboratory accreditation program. The study was initiated to determine calibration factors for both types of phantoms and to evaluate the suitability of their use in DOE Laboratory Accreditation Program (DOELAP) round-robin testing. The BOMAB was found to be more appropriate for the DOELAP testing program. 9 refs., 9 figs., 9 tabs.

  10. The effect of fission products on the rate of U3O8 formation in SIMFUEL oxidized in air at 250°C

    NASA Astrophysics Data System (ADS)

    Choi, Jong-Won; McEachern, Rod J.; Taylor, Peter; Wood, Donald D.

    1996-06-01

    The effect of fission products on the rate of U3O8 formation was investigated by oxidizing UO2-based SIMFUEL (simulated high burnup nuclear fuel) and unirradiated UO2 fuel specimens in air at 250°C for different times (1-317 days). The progress of oxidation was monitored by X-ray diffraction, revealing that the rate of U3O8 formation declines with increasing burnup. An expression was derived to describe quantitatively the time for U3O8 powder formation as a function of simulated burnup. These findings were supported by additional isochronal oxidation experiments conducted between 200 and 300°C.

  11. Measurements of yields of fission products in the reaction of {sup 238}U with high-energy p, d and n beams

    SciTech Connect

    Nolen, J.A.; Ahmad, I.; Back, B.B.

    1995-08-01

    An experiment was performed at the Michigan State University cyclotron to determine the yields of neutron-rich fission products in the reaction of {sup 238}U with 100-MeV neutrons, 200-MeV deuterons and 200-MeV protons. Several 1-mm-thick {sup 238}U foils were irradiated for 100-second intervals sequentially for each configuration and the ten spectra were added for higher statistics. The three successive spectra, each for a 40 s period, were accumulated for each sample. Ten foils were irradiated. Successive spectra allowed us to determine approximate half-lives of the gamma peaks. Several arrangements, which were similar to the setup we plan to use in our radioactive beam proposal, were used for the production of fission products. For the high-energy neutron irradiation, U foils were placed after a 5-inch-long, 1-inch-diameter Be cylinder which stopped the 200-MeV deuteron beam generating 100-MeV neutrons. Arrangements for deuteron irradiation included direct irradiation of U foils, placing U foils after different lengths of (0.5 inch, 1.0 inch and 1.5 inch) 2-inch diameter U cylinder. Since the deuteron range in uranium is 17 mm, some of the irradiations were due to the secondary neutrons from the deuteron-induced fission of U. Similar arrangements were also used for the 200-MeV proton irradiation of the {sup 238}U foils. In all cases, several neutron-rich fission products were identified and their yields determined. In particular, we were able to observe Sn in all the runs and determine its yield. The data show that with our proposed radioactive device we will be able to produce more than 10{sup 12} {sup 132}Sn atoms per second in the target. Assuming an overall efficiency of 1 %, we will be able to deliver one particle nanoampere of {sup 132}Sn beam at a target location. Detailed analysis of the {gamma}-ray spectra is in progress.

  12. Spallation reaction study for fission products in nuclear waste: Cross section measurements for 137Cs, 90Sr and 107Pd on proton and deuteron

    NASA Astrophysics Data System (ADS)

    Wang, He; Otsu, Hideaki; Sakurai, Hiroyoshi; Ahn, DeukSoon; Aikawa, Masayuki; Ando, Takashi; Araki, Shouhei; Chen, Sidong; Chiga, Nobuyuki; Doornenbal, Pieter; Fukuda, Naoki; Isobe, Tadaaki; Kawakami, Shunsuke; Kawase, Shoichiro; Kin, Tadahiro; Kondo, Yosuke; Koyama, Shupei; Kubono, Shigeru; Maeda, Yukie; Makinaga, Ayano; Matsushita, Masafumi; Matsuzaki, Teiichiro; Michimasa, Shinichiro; Momiyama, Satoru; Nagamine, Shunsuke; Nakamura, Takashi; Nakano, Keita; Niikura, Megumi; Ozaki, Tomoyuki; Saito, Atsumi; Saito, Takeshi; Shiga, Yoshiaki; Shikata, Mizuki; Shimizu, Yohei; Shimoura, Susumu; Sumikama, Toshiyuki; Söderström, Pär-Anders; Suzuki, Hiroshi; Takeda, Hiroyuki; Takeuchi, Satoshi; Taniuchi, Ryo; Togano, Yasuhiro; Tsubota, Junichi; Uesaka, Meiko; Watanabe, Yasushi; Watanabe, Yukinobu; Wimmer, Kathrin; Yamamoto, Tatsuya; Yoshida, Koichi

    2017-09-01

    Spallation reactions for the long-lived fission products 137Cs, 90Sr and 107Pd have been studied for the purpose of nuclear waste transmutation. The cross sections on the proton- and deuteron-induced spallation were obtained in inverse kinematics at the RIKEN Radioactive Isotope Beam Factory. Both the target and energy dependences of cross sections have been investigated systematically. and the cross-section differences between the proton and deuteron are found to be larger for lighter fragments. The experimental data are compared with the SPACS semi-empirical parameterization and the PHITS calculations including both the intra-nuclear cascade and evaporation processes.

  13. New neutron-rich microsecond isomers observed among fission products of {sup 238}U at 80 MeV/nucleon

    SciTech Connect

    Folden, C. M. III; Ginter, T. N.; Hausmann, M.; Portillo, M.; Nettleton, A. S.; Amthor, A. M.; Sherrill, B. M.; Kubo, T.; Takeda, H.; Loveland, W.; Manikonda, S. L.; Morrissey, D. J.; Nakao, T.; Souliotis, G. A.; Strong, B. F.; Tarasov, O. B.

    2009-06-15

    Eight new isomeric states in neutron-rich nuclides have been discovered in fission fragments produced by the reaction of an 80 MeV/nucleon {sup 238}U beam with a {sup 9}Be target and separated in-flight using the A1900 fragment separator. The experiment was conducted at the National Superconducting Cyclotron Laboratory (NSCL) at Michigan State University. Gamma rays were detected in a high-purity germanium detector located at the focal plane within a time window of 20 {mu}s following ion implantation. In some cases the isomers were observed to decay into previously reported states, allowing us to assign the initial decay from the isomeric state. Among the outcomes, the results suggest that many studies on the nuclear structure of medium-mass neutron-rich nuclei are feasible at projectile fragmentation facilities using induced fission.

  14. Air Activation Following an Atmospheric Explosion

    SciTech Connect

    Lowrey, Justin D.; McIntyre, Justin I.; Prichard, Andrew W.; Gesh, Christopher J.

    2013-03-13

    In addition to thermal radiation and fission products, nuclear explosions result in a very high flux of unfissioned neutrons. Within an atmospheric nuclear explosion, these neutrons can activate the various elemental components of natural air, potentially adding to the radioactive signature of the event as a whole. The goal of this work is to make an order-of-magnitude estimate of the total amount of air activation products that can result from an atmospheric nuclear explosion.

  15. Event-by-Event Fission Modeling of Prompt Neutrons and Photons from Neutron-Induced and Spontaneous Fission with FREYA

    NASA Astrophysics Data System (ADS)

    Vogt, Ramona; Randrup, Jorgen

    2013-04-01

    The event-by-event fission Monte Carlo code FREYA (Fission Reaction Event Yield Algorithm) generates large samples of complete fission events. Using FREYA, it is possible to obtain the fission products as well as the prompt neutrons and photons emitted during the fission process, all with complete kinematic information. We can therefore extract any desired correlation observables. Concentrating on ^239Pu(n,f), ^240Pu(sf) and ^252Cf(sf), we compare our FREYA results with available data on prompt neutron and photon emission and present predictions for novel fission observables that could be measured with modern detectors.

  16. The Sentinel-4 Mission: Instrument Description and Atmospheric Composition Products

    NASA Astrophysics Data System (ADS)

    Veihelmann, Ben; Meijer, Yasjka; Ingmann, Paul; Koopman, Rob; Bazalgette Courrèges-Lacoste, Grégory; Stark, Hendrik

    2013-04-01

    The Sentinel-4 mission, together with Sentinel-5 and the Sentinel-5 Precursor missions, is part of the Global Monitoring for Environment and Security (GMES) space component covering the Earth's atmosphere. The primary objective of the Sentinel-4 mission is the observation of the diurnal cycle of tropospheric species in support of the air quality applications of GMES Atmosphere Services. The presentation focuses on the Sentinel-4/UVN instrument and its related Level-2 atmospheric composition products. The Sentinel-4 instrument is an Ultra-violet Visible Near infrared spectrometer (S4/UVN) which is embarked on the geostationary Meteosat Third Generation-Sounder (MTG-S) platforms. Key features of the S4/UVN instrument are the spectral range from 305 nm to 500 nm with a spectral resolution of 0.5 nm, and from 750 nm to 775 nm with a spectral resolution of 0.12 nm, in combination with a low polarization sensitivity and a high radiometric accuracy. The instrument shall observe Europe with a revisit time of one hour. The spatial sampling distance varies across the geographic coverage area and takes a value of 8 km at a reference location at 45˚ N. The expected launch date of the first MTG-S platform is 2019, and the expected lifetime is 15 years (two S4/UVN instruments in sequence on two MTG-S platforms). ESA will develop products based on the S4/UVN measurements for the key target species, which are NO2, O3, HCHO, SO2, aerosols, and CHOCHO, and for cloud and surface properties (mainly intermediate products). Also a synergetic O3 vertical profile product is foreseen based on observations from the S4/UVN and the MTG InfraRed Sounder (IRS) on-board the same platform. Synergetic aerosol and cloud products are foreseen based on observations from the S4/UVN and from the MTG Flexible Combined Imager (FCI) on-board the MTG-Imager (MTG-I) platform. Current pre-development studies are dedicated to a daily surface reflectance map product that treats the surface directionality as

  17. Nuclear Power from Fission Reactors. An Introduction.

    ERIC Educational Resources Information Center

    Department of Energy, Washington, DC. Technical Information Center.

    The purpose of this booklet is to provide a basic understanding of nuclear fission energy and different fission reaction concepts. Topics discussed are: energy use and production, current uses of fuels, oil and gas consumption, alternative energy sources, fossil fuel plants, nuclear plants, boiling water and pressurized water reactors, the light…

  18. Fission yeast ATF/CREB family protein Atf21 plays important roles in production of normal spores.

    PubMed

    Morita, Tomohiko; Yamada, Takatomi; Yamada, Shintaro; Matsumoto, Kouji; Ohta, Kunihiro

    2011-02-01

    Activating transcription factor/cAMP response element binding protein (ATF/CREB) family transcription factors play central roles in maintaining cellular homeostasis. They are activated in response to environmental stimuli, bind to CRE sequences in the promoters of stress-response genes and regulate transcription. Although ATF/CREB proteins are widely conserved among most eukaryotes, their characteristics are highly diverse. Here, we investigated the functions of a fission yeast ATF/CREB protein Atf21 to find out its unique properties. We show that Atf21 is dispensable for the adaptive response to several stresses such as nitrogen starvation and for meiotic events including nuclear divisions. However, spores derived from atf21Δ mutants are not as mature as wild-type ones and are unable to form colonies under nutrition-rich conditions. Furthermore, we demonstrate that the Atf21 protein, which is scarce in early meiosis, gradually accumulates as meiosis proceeds; it reaches maximum levels approximately 8 h after nitrogen starvation and is present during germination. These results suggest that Atf21 is expressed and functions long after nitrogen starvation. Given that other well-characterized fission yeast ATF/CREB proteins Atf1 and Pcr1 accumulate and function promptly upon exposure to environmental stresses, we propose that Atf21 is a distinct member of the ATF/CREB family in fission yeast. © 2010 The Authors. Journal compilation © 2010 by the Molecular Biology Society of Japan/Blackwell Publishing Ltd.

  19. First-principles study of fission product (Xe, Cs, Sr) incorporation and segregation in alkaline earth metal oxides, HfO2, and MgO-HfO2 interface

    SciTech Connect

    Liu, Xiang-yang; Uberuaga, Blas P; Sickafus, Kurt E

    2008-01-01

    In order to close the nuclear fuel cycle, advanced concepts for separating out fission products are necessary. One approach is to use a dispersion fuel form in which a fissile core is surrounded by an inert matrix that captures and immobilizes the fission products from the core. If this inert matrix can be easily separated from the fuel, via e.g. solution chemistry, the fission products can be separated from the fissile material. We examine a surrogate dispersion fuel composition, in which hafnia (HfO{sub 2}) is a surrogate for the fissile core and alkaline earth metal oxides are used as the inert matrix. The questions of fission product incorporation in these oxides and possible segregation behavior at interfaces are considered. Density functional theory based calculations for fission product elements (Xe, Sr, and Cs) in these oxides are carried out. We find smaller incorporation energy in hafnia than in MgO for Cs and Sr, and Xe if variation of charge state is allowed. We also find that this trend is reversed or reduced for alkaline earth metal oxides with large cation sizes. Model interfacial calculations show a strong tendency of segregation from bulk MgO to MgO-HfO{sub 2} interfaces.

  20. Fuel and fission product behaviour in early phases of a severe accident. Part II: Interpretation of the experimental results of the PHEBUS FPT2 test

    NASA Astrophysics Data System (ADS)

    Dubourg, R.; Barrachin, M.; Ducher, R.; Gavillet, D.; De Bremaecker, A.

    2014-10-01

    One objective of the FPT2 test of the PHEBUS FP Program was to study the degradation of an irradiated UO2 fuel bundle and the fission product behaviour under conditions of low steam flow. The results of the post-irradiation examinations (PIE) at the upper levels (823 mm and 900 mm) of the test section previously reported are interpreted in the present paper. Solid state interactions between fuel and cladding have been compared with the characteristics of interaction identified in the previous separate-effect tests. Corium resulting from the interaction between fuel and cladding was formed. The uranium concentration in the corium is compared to analytical tests and a scenario for the corium formation is proposed. The analysis showed that, despite the rather low fuel burn up, the conditions of temperature and oxygen potential reached during the starvation phase are able to give an early very significant release fraction of caesium. A significant part (but not all) of the molybdenum was segregated at grain boundaries and trapped in metallic inclusions from which they were totally removed in the final part of the experiment. During the steam starvation phase, the conditions of oxygen potential were favourable for the formation of simple Ba and BaO chemical forms but the temperature was too low to provoke their volatility. This is one important difference with out-of-pile experiments such as VERCORS for which only a combination of high temperature and low oxygen potential induced a significant barium release. Finally another significant difference with analytical out-of-pile experiments comes from the formation of foamy zones due to the fission gas presence in FPT2-type experiments which give an additional possibility for the formation of stable fission product compounds.

  1. Gas Sensor Evaluations in Polymer Combustion Product Atmospheres

    NASA Technical Reports Server (NTRS)

    Delgado, Rafael H.; Davis, Dennis D.; Beeson, Harold D.

    1999-01-01

    Toxic gases produced by the combustion or thermo-oxidative degradation of materials such as wire insulation, foam, plastics, or electronic circuit boards in space shuttle or space station crew cabins may pose a significant hazard to the flight crew. Toxic gas sensors are routinely evaluated in pure gas standard mixtures, but the possible interferences from polymer combustion products are not routinely evaluated. The NASA White Sands Test Facility (WSTF) has developed a test system that provides atmospheres containing predetermined quantities of target gases combined with the coincidental combustion products of common spacecraft materials. The target gases are quantitated in real time by infrared (IR) spectroscopy and verified by grab samples. The sensor responses are recorded in real time and are compared to the IR and validation analyses. Target gases such as carbon monoxide, hydrogen cyanide, hydrogen chloride, and hydrogen fluoride can be generated by the combustion of poly(vinyl chloride), polyimide-fluoropolymer wire insulation, polyurethane foam, or electronic circuit board materials. The kinetics and product identifications for the combustion of the various materials were determined by thermogravimetric-IR spectroscopic studies. These data were then scaled to provide the required levels of target gases in the sensor evaluation system. Multisensor toxic gas monitors from two manufacturers were evaluated using this system. In general, the sensor responses satisfactorily tracked the real-time concentrations of toxic gases in a dynamic mixture. Interferences from a number of organic combustion products including acetaldehyde and bisphenol-A were minimal. Hydrogen bromide in the products of circuit board combustion registered as hydrogen chloride. The use of actual polymer combustion atmospheres for the evaluation of sensors can provide additional confidence in the reliability of the sensor response.

  2. Benz[a]anthracene biotransformation and production of ring fission products by Sphingobium sp. strain KK22.

    PubMed

    Kunihiro, Marie; Ozeki, Yasuhiro; Nogi, Yuichi; Hamamura, Natsuko; Kanaly, Robert A

    2013-07-01

    A soil bacterium, designated strain KK22, was isolated from a phenanthrene enrichment culture of a bacterial consortium that grew on diesel fuel, and it was found to biotransform the persistent environmental pollutant and high-molecular-weight polycyclic aromatic hydrocarbon (PAH) benz[a]anthracene. Nearly complete sequencing of the 16S rRNA gene of strain KK22 and phylogenetic analysis revealed that this organism is a new member of the genus Sphingobium. An 8-day time course study that consisted of whole-culture extractions followed by high-performance liquid chromatography (HPLC) analyses with fluorescence detection showed that 80 to 90% biodegradation of 2.5 mg liter(-1) benz[a]anthracene had occurred. Biodegradation assays where benz[a]anthracene was supplied in crystalline form (100 mg liter(-1)) confirmed biodegradation and showed that strain KK22 cells precultured on glucose were equally capable of benz[a]anthracene biotransformation when precultured on glucose plus phenanthrene. Analyses of organic extracts from benz[a]anthracene biodegradation by liquid chromatography negative electrospray ionization tandem mass spectrometry [LC/ESI(-)-MS/MS] revealed 10 products, including two o-hydroxypolyaromatic acids and two hydroxy-naphthoic acids. 1-Hydroxy-2- and 2-hydroxy-3-naphthoic acids were unambiguously identified, and this indicated that oxidation of the benz[a]anthracene molecule occurred via both the linear kata and angular kata ends of the molecule. Other two- and single-aromatic-ring metabolites were also documented, including 3-(2-carboxyvinyl)naphthalene-2-carboxylic acid and salicylic acid, and the proposed pathways for benz[a]anthracene biotransformation by a bacterium were extended.

  3. Benz[a]anthracene Biotransformation and Production of Ring Fission Products by Sphingobium sp. Strain KK22

    PubMed Central

    Kunihiro, Marie; Ozeki, Yasuhiro; Nogi, Yuichi; Hamamura, Natsuko

    2013-01-01

    A soil bacterium, designated strain KK22, was isolated from a phenanthrene enrichment culture of a bacterial consortium that grew on diesel fuel, and it was found to biotransform the persistent environmental pollutant and high-molecular-weight polycyclic aromatic hydrocarbon (PAH) benz[a]anthracene. Nearly complete sequencing of the 16S rRNA gene of strain KK22 and phylogenetic analysis revealed that this organism is a new member of the genus Sphingobium. An 8-day time course study that consisted of whole-culture extractions followed by high-performance liquid chromatography (HPLC) analyses with fluorescence detection showed that 80 to 90% biodegradation of 2.5 mg liter−1 benz[a]anthracene had occurred. Biodegradation assays where benz[a]anthracene was supplied in crystalline form (100 mg liter−1) confirmed biodegradation and showed that strain KK22 cells precultured on glucose were equally capable of benz[a]anthracene biotransformation when precultured on glucose plus phenanthrene. Analyses of organic extracts from benz[a]anthracene biodegradation by liquid chromatography negative electrospray ionization tandem mass spectrometry [LC/ESI(−)-MS/MS] revealed 10 products, including two o-hydroxypolyaromatic acids and two hydroxy-naphthoic acids. 1-Hydroxy-2- and 2-hydroxy-3-naphthoic acids were unambiguously identified, and this indicated that oxidation of the benz[a]anthracene molecule occurred via both the linear kata and angular kata ends of the molecule. Other two- and single-aromatic-ring metabolites were also documented, including 3-(2-carboxyvinyl)naphthalene-2-carboxylic acid and salicylic acid, and the proposed pathways for benz[a]anthracene biotransformation by a bacterium were extended. PMID:23686261

  4. Gasdynamic propagation of rocket exhaust products in the upper atmosphere

    NASA Astrophysics Data System (ADS)

    Molchanov, A. G.; Platov, Yu. V.

    2011-12-01

    The dispersion of exhaust products of rocket fuel in the direction perpendicular to the motion of a rocket is investigated in this work. A comparison of the results of numerical calculations with a self-similar approximation of a strong cylindrically symmetric explosion is fulfilled. It is shown that at sufficiently high rocket velocity V ∞, which exceeds the sum of gas exhaust velocity V e from the nozzle and sound speed V s ( V ∞ > V e + V s ), a gasdynamic hole can arise around the rocket trajectory in the upper atmosphere, inside which the total concentration of gas becomes less than the equilibrium concentration of gas at a given altitude. The dynamics of the profiles of density and temperature of the exhaust products inside a rocket plume is calculated.

  5. The seventh international conference on the chemistry and migration behavior of actinides and fission products in the Geosphere MIGRATION'99 abstracts

    SciTech Connect

    Palmer, C

    1999-09-01

    The Migration conferences focus on recent developments in the fundamental chemistry of actinides and fission products in natural aquifer systems, their interactions and migration in the geosphere, and the processes involved in modeling their geochemical behavior. The primary mode dissemination of technical information will be early evening poster sessions designed to encourage intensive communication between the authors and participants. Daily oral sessions will be opened with invited lectures followed by contributed papers within the scope of each session. Sessions cover: (A) Chemistry of actinides and fission products in natural aquatic systems: (1) Solubilities and dissolution reactions; (2) Complexation with inorganic and organic ligands; (3) Redox reactions; (4) Colloid formation; and (5) Experimental methods. (B) Geochemical interactions and transport phenomena: (1) Diffusion and migration in geologic media; (2) Sorption/desorption phenomena; (3) Natural analog studies; (4) Effects of biological activities and organic materials; (5) Colloid transport; (6) Radionuclides in soils; and (7) Soil-remediation chemistries. (C) Data base development and modeling: (1) Data selection and evaluation; (2) Data base management; (3) Geochemical models and modeling; (4) Application of models; and (5) Validation of modeling results.

  6. Diversification of 99Mo/99mTc separation: non–fission reactor production of 99Mo as a strategy for enhancing 99mTc availability.

    PubMed

    Pillai, Maroor R A; Dash, Ashutosh; Knapp, Furn F Russ

    2015-01-01

    This paper discusses the benefits of obtaining (99m)Tc from non-fission reactor-produced low-specific-activity (99)Mo. This scenario is based on establishing a diversified chain of facilities for the distribution of (99m)Tc separated from reactor-produced (99)Mo by (n,γ) activation of natural or enriched Mo. Such facilities have expected lower investments than required for the proposed chain of cyclotrons for the production of (99m)Tc. Facilities can receive and process reactor-irradiated Mo targets then used for extraction of (99m)Tc over a period of 2 wk, with 3 extractions on the same day. Estimates suggest that a center receiving 1.85 TBq (50 Ci) of (99)Mo once every 4 d can provide 1.48-3.33 TBq (40-90 Ci) of (99m)Tc daily. This model can use research reactors operating in the United States to supply current (99)Mo needs by applying natural (nat)Mo targets. (99)Mo production capacity can be enhanced by using (98)Mo-enriched targets. The proposed model reduces the loss of (99)Mo by decay and avoids proliferation as well as waste management issues associated with fission-produced (99)Mo.

  7. Effect of the β decay of metallic fission products on the chemical and phase compositions of the uranium-plutonium nitride nuclear fuel irradiated by fast neutrons

    NASA Astrophysics Data System (ADS)

    Bondarenko, G. G.; Androsov, A. V.; Bulatov, G. S.; Gedgovd, K. N.; Lyubimov, D. Yu.; Yakunkin, M. M.

    2016-09-01

    Thermodynamic analysis of the chemical and phase compositions of uranium-plutonium nitride (U0.8Pu0.2)N0.995 irradiated by fast neutrons to a burn-up fraction of 14% shows that a structure, which consists of a solid solution based on uranium and plutonium nitrides and containing some elements (americium, neptunium, zirconium, yttrium, lanthanides), individual condensed phases (U2N3, CeRu2, Ba3N2, CsI, Sr3N2, LaSe), metallic molybdenum and technetium, and U(Ru, Rh, Pd)3 intermetallics, forms due to the accumulation of metallic fission products. The contents and compositions of these phases are calculated. The change in the chemical and phase compositions of the irradiated uranium-plutonium nitride during the β decay of metallic radioactive fission products is studied. The kinetics of the transformations of 95Nb41N, 143Pr59N, 151Sm62N, and 147NdN into 95Mo42 + Ns.s., 143Nd60N, 151Eu63N, and 147SmN, respectively, is calculated.

  8. USA/FRG umbrella agreement for cooperation in GCR [Gas Cooled Reactor] development: Fuel, fission products and graphite subprogram. Part 1, Management meeting report: Part 2, Revised subprogram plan, Revision 10

    SciTech Connect

    1986-05-01

    This Subprogram Plan describes cooperative work in the areas of HTR fuel and graphite development and fission product studies that is being carried out under US/FRG/Swiss Implementing Agreement for cooperation in Gas Cooled Reactor development. Only bilateral US/FRG cooperation is included, since it is the only active work in this subprogram area at this time. The cooperation has been in progress since February 1977. A number of Project Work Statements have been developed in each of the major areas of the subprogram, and work on many of them is in progress. The following specific areas are included in the scope of this plan: fuel development; graphite development; fission product release; and fission product behavior outside the fuel elements.

  9. Impact of Modular Total Absorption Spectrometer measurements of β decay of fission products on the decay heat and reactor ν¯e flux calculation

    NASA Astrophysics Data System (ADS)

    Fijałkowska, A.; Karny, M.; Rykaczewski, K. P.; Rasco, B. C.; Grzywacz, R.; Gross, C. J.; Wolińska-Cichocka, M.; Goetz, K. C.; Stracener, D. W.; Bielewski, W.; Goans, R.; Hamilton, J. H.; Johnson, J. W.; Jost, C.; Madurga, M.; Miernik, K.; Miller, D.; Padgett, S. W.; Paulauskas, S. V.; Ramayya, A. V.; Zganjar, E. F.

    2017-08-01

    We report the results of a β -decay study of fission products Br 86 , Kr 89 , Rb 89 , Rb 90 g s , Rbm90 , Kr 90 , Rb 92 , Xe 139 , and Cs 142 performed with the Modular Total Absorption Spectrometer (MTAS) and on-line mass-separated ion beams. These radioactivities were assessed by the Nuclear Energy Agency as having high priority for decay heat analysis during a nuclear fuel cycle. We observe a substantial increase in β feeding to high excited states in all daughter isotopes in comparison to earlier data. This increases the average γ -ray energy emitted by the decay of fission fragments during the first 10 000 s after fission of U 235 and Pu 239 by approximately 2% and 1%, respectively, improving agreement between results of calculations and direct observations. New MTAS results reduce the reference reactor ν¯e flux used to analyze reactor ν¯e interaction with detector matter. The reduction determined by the ab initio method for the four nuclear fuel components, U 235 , U 238 , Pu 239 , and Pu 241 , amounts to 0.976, 0.986, 0.983, and 0.984, respectively.

  10. Atmospheric photooxidation of alkylbenzenes—I. Carbonyl product analyses

    NASA Astrophysics Data System (ADS)

    Yu, Jianzhen; Jeffries, Harvey E.; Sexton, Kenneth G.

    Six alkylbenzenes—toluene, p-xylene, m-xylene, o-xylene, 1,3,5-trimethylbenzene and 1,2,4-trimethylbenzene—were selected to investigate the carbonyl products resulting from OH-initiated oxidation of aromatic compounds. Experiments were conducted in both indoor and outdoor smog chambers under simulated atmospheric conditions. Both batch samples and 30 min interval samples were taken in the outdoor smog chamber experiments using 1 ppmV alkylbenzene, 0.67 ppm NO x and sunlight as the light source. A wide variety of carbonyl products were detected and identified using gas chromatography/mass spectrometric (GC/MS) detection by their O-(2,3,4,5,6-pentafluorobenzyl)-hydroxylamine (PFBHA) derivatives. Among the observed carbonyl products are aromatic aldehydes, quinones, di-unsaturated 1,6-dicarbonyls, unsaturated 1,4-dicarbonyls, saturated dicarbonyls, hydroxy dicarbonyls, glycolaldehyde, hydroxy acetone, and possibly triones and epoxy carbonyls. Quantification was achieved using 13C 3-acetone as a gas-phase internal standard. The numerous carbonyl products detected in itself partially explain previous difficulties in balancing the reacted carbon. They also provide additional insight into the oxidation mechanism for aromatic compounds, which will be discussed in this paper.

  11. Thorium-uranium fission radiography

    NASA Technical Reports Server (NTRS)

    Haines, E. L.; Weiss, J. R.; Burnett, D. S.; Woolum, D. S.

    1976-01-01

    Results are described for studies designed to develop routine methods for in-situ measurement of the abundance of Th and U on a microscale in heterogeneous samples, especially rocks, using the secondary high-energy neutron flux developed when the 650 MeV proton beam of an accelerator is stopped in a 42 x 42 cm diam Cu cylinder. Irradiations were performed at three different locations in a rabbit tube in the beam stop area, and thick metal foils of Bi, Th, and natural U as well as polished silicate glasses of known U and Th contents were used as targets and were placed in contact with mica which served as a fission track detector. In many cases both bare and Cd-covered detectors were exposed. The exposed mica samples were etched in 48% HF and the fission tracks counted by conventional transmitted light microscopy. Relative fission cross sections are examined, along with absolute Th track production rates, interaction tracks, and a comparison of measured and calculated fission rates. The practicality of fast neutron radiography revealed by experiments to data is discussed primarily for Th/U measurements, and mixtures of other fissionable nuclei are briefly considered.

  12. Thorium-uranium fission radiography

    NASA Technical Reports Server (NTRS)

    Haines, E. L.; Weiss, J. R.; Burnett, D. S.; Woolum, D. S.

    1976-01-01

    Results are described for studies designed to develop routine methods for in-situ measurement of the abundance of Th and U on a microscale in heterogeneous samples, especially rocks, using the secondary high-energy neutron flux developed when the 650 MeV proton beam of an accelerator is stopped in a 42 x 42 cm diam Cu cylinder. Irradiations were performed at three different locations in a rabbit tube in the beam stop area, and thick metal foils of Bi, Th, and natural U as well as polished silicate glasses of known U and Th contents were used as targets and were placed in contact with mica which served as a fission track detector. In many cases both bare and Cd-covered detectors were exposed. The exposed mica samples were etched in 48% HF and the fission tracks counted by conventional transmitted light microscopy. Relative fission cross sections are examined, along with absolute Th track production rates, interaction tracks, and a comparison of measured and calculated fission rates. The practicality of fast neutron radiography revealed by experiments to data is discussed primarily for Th/U measurements, and mixtures of other fissionable nuclei are briefly considered.

  13. Ballistic piston fissioning plasma experiment.

    NASA Technical Reports Server (NTRS)

    Miller, B. E.; Schneider, R. T.; Thom, K.; Lalos, G. T.

    1971-01-01

    The production of fissioning uranium plasma samples such that the fission fragment stopping distance is less than the dimensions of the plasma is approached by using a ballistic piston device for the compression of uranium hexafluoride. The experimental apparatus is described. At room temperature the gun can be loaded up to 100 torr UF6 partial pressure, but at compression a thousand fold increase of pressure can be obtained at a particle density on the order of 10 to the 19th power per cu cm. Limited spectral studies of UF6 were performed while obtaining the pressure-volume data. The results obtained and their implications are discussed.

  14. Status of fission yield data

    SciTech Connect

    England, T.R.; Blachot, J.

    1988-01-01

    In this paper we summarize the current status of the recent US evaluation for 34 fissioning nuclides at one or more neutron incident energies and for spontaneous fission. Currently there are 50 yields sets, and for each we have independent and cumulative yields and uncertainties for approximately 1100 fission products. When finalized the recommended data will become part of Version VI of the US ENDF/B. Other major evaluations in progress that are included in a recently formed IAEA Coordinated Research Program are also summarized. In a second part we review two empirical models in use to estimate independent yields. Comparison of model estimates with measured data is presented, including a comparison with some recent data obtained from Lohengrin (Cf-249 T). 18 refs., 13 figs., 3 tabs.

  15. Energy dependence of fission product yields from 235U, 238U and 239Pu for incident neutron energies between 0.5 and 14.8 MeV

    DOE PAGES

    Gooden, M. E.; Arnold, C. W.; Becker, J. A.; ...

    2016-01-06

    In this study, Fission Product Yields (FPY) have historically been one of the most observable features of the fission process. They are known to have strong variations that are dependent on the fissioning species, the excitation energy, and the angular momentum of the compound system. However, consistent and systematic studies of the variation of these FPY with energy have proved challenging. This is caused primarily by the nature of the experiments that have traditionally relied on radiochemical procedures to isolate specific fission products. Although radiochemical procedures exist that can isolate all products, each element presents specific challenges and introduces varyingmore » degrees of systematic errors that can make inter-comparison of FPY uncertain. Although of high importance in fields such as nuclear forensics and Stockpile Stewardship, accurate information about the energy dependence of neutron induced FPY are sparse, due primarily to the lack of suitable monoenergetic neutron sources. There is a clear need for improved data, and to address this issue, a collaboration was formed between Los Alamos National Laboratory (LANL), Lawrence Livermore National Laboratory (LLNL) and the Triangle Universities Nuclear Laboratory (TUNL) to measure the energy dependence of FPY for 235U, 238U and 239Pu. The measurements have been performed at TUNL, using a 10 MV Tandem Van de Graaff accelerator to produce monoenergetic neutrons at energies between 0.6 MeV to 14.8 MeV through a variety of reactions. The measurements have utilized a dual-fission chamber, with thin (10-100 μg/cm2) reference foils of similar material to a thick (100-400 mg) activation target held in the center between the chambers. This method allows for the accurate determination of the number of fissions that occurred in the thick target without requiring knowledge of the fission cross section or neutron fluence on target. Following activation, the thick target was removed from the dual-fission

  16. Energy dependence of fission product yields from 235U, 238U and 239Pu for incident neutron energies between 0.5 and 14.8 MeV

    SciTech Connect

    Gooden, M. E.; Arnold, C. W.; Becker, J. A.; Bhatia, C.; Bhike, M.; Bond, E. M.; Bredeweg, T. A.; Fallin, B.; Fowler, M. M.; Howell, C. R.; Kelley, J. H.; Krishichayan, .; Macri, R.; Rusev, G.; Ryan, C.; Sheets, S. A.; Stoyer, M. A.; Tonchev, A. P.; Tornow, W.; Vieira, D. J.; Wilhelmy, J. B.

    2016-01-06

    In this study, Fission Product Yields (FPY) have historically been one of the most observable features of the fission process. They are known to have strong variations that are dependent on the fissioning species, the excitation energy, and the angular momentum of the compound system. However, consistent and systematic studies of the variation of these FPY with energy have proved challenging. This is caused primarily by the nature of the experiments that have traditionally relied on radiochemical procedures to isolate specific fission products. Although radiochemical procedures exist that can isolate all products, each element presents specific challenges and introduces varying degrees of systematic errors that can make inter-comparison of FPY uncertain. Although of high importance in fields such as nuclear forensics and Stockpile Stewardship, accurate information about the energy dependence of neutron induced FPY are sparse, due primarily to the lack of suitable monoenergetic neutron sources. There is a clear need for improved data, and to address this issue, a collaboration was formed between Los Alamos National Laboratory (LANL), Lawrence Livermore National Laboratory (LLNL) and the Triangle Universities Nuclear Laboratory (TUNL) to measure the energy dependence of FPY for 235U, 238U and 239Pu. The measurements have been performed at TUNL, using a 10 MV Tandem Van de Graaff accelerator to produce monoenergetic neutrons at energies between 0.6 MeV to 14.8 MeV through a variety of reactions. The measurements have utilized a dual-fission chamber, with thin (10-100 μg/cm2) reference foils of similar material to a thick (100-400 mg) activation target held in the center between the chambers. This method allows for the accurate determination of the number of fissions that occurred in the thick target without requiring knowledge of the fission cross section or neutron fluence on target. Following activation, the thick target was removed

  17. Energy Dependence of Fission Product Yields from {sup 235}U, {sup 238}U and {sup 239}Pu for Incident Neutron Energies Between 0.5 and 14.8 MeV

    SciTech Connect

    Gooden, M.E.; Arnold, C.W.; Becker, J.A.; Bhatia, C.; Bhike, M.; Bond, E.M.; Bredeweg, T.A.; Fallin, B.; Fowler, M.M.; Howell, C.R.; Kelley, J.H.; Krishichayan; Macri, R.; Rusev, G.; Ryan, C.; Sheets, S.A.; Stoyer, M.A.; Tonchev, A.P.; Tornow, W.; and others

    2016-01-15

    Fission Product Yields (FPY) have historically been one of the most observable features of the fission process. They are known to have strong variations that are dependent on the fissioning species, the excitation energy, and the angular momentum of the compound system. However, consistent and systematic studies of the variation of these FPY with energy have proved challenging. This is caused primarily by the nature of the experiments that have traditionally relied on radiochemical procedures to isolate specific fission products. Although radiochemical procedures exist that can isolate all products, each element presents specific challenges and introduces varying degrees of systematic errors that can make inter-comparison of FPY uncertain. Although of high importance in fields such as nuclear forensics and Stockpile Stewardship, accurate information about the energy dependence of neutron induced FPY are sparse, due primarily to the lack of suitable monoenergetic neutron sources. There is a clear need for improved data, and to address this issue, a collaboration was formed between Los Alamos National Laboratory (LANL), Lawrence Livermore National Laboratory (LLNL) and the Triangle Universities Nuclear Laboratory (TUNL) to measure the energy dependence of FPY for {sup 235}U, {sup 238}U and {sup 239}Pu. The measurements have been performed at TUNL, using a 10 MV Tandem Van de Graaff accelerator to produce monoenergetic neutrons at energies between 0.6 MeV to 14.8 MeV through a variety of reactions. The measurements have utilized a dual-fission chamber, with thin (10-100 μg/cm2) reference foils of similar material to a thick (100-400 mg) activation target held in the center between the chambers. This method allows for the accurate determination of the number of fissions that occurred in the thick target without requiring knowledge of the fission cross section or neutron fluence on target. Following activation, the thick target was removed from the dual-fission chamber

  18. Energy Dependence of Fission Product Yields from 235U, 238U and 239Pu for Incident Neutron Energies Between 0.5 and 14.8 MeV

    NASA Astrophysics Data System (ADS)

    Gooden, M. E.; Arnold, C. W.; Becker, J. A.; Bhatia, C.; Bhike, M.; Bond, E. M.; Bredeweg, T. A.; Fallin, B.; Fowler, M. M.; Howell, C. R.; Kelley, J. H.; Krishichayan; Macri, R.; Rusev, G.; Ryan, C.; Sheets, S. A.; Stoyer, M. A.; Tonchev, A. P.; Tornow, W.; Vieira, D. J.; Wilhelmy, J. B.

    2016-01-01

    Fission Product Yields (FPY) have historically been one of the most observable features of the fission process. They are known to have strong variations that are dependent on the fissioning species, the excitation energy, and the angular momentum of the compound system. However, consistent and systematic studies of the variation of these FPY with energy have proved challenging. This is caused primarily by the nature of the experiments that have traditionally relied on radiochemical procedures to isolate specific fission products. Although radiochemical procedures exist that can isolate all products, each element presents specific challenges and introduces varying degrees of systematic errors that can make inter-comparison of FPY uncertain. Although of high importance in fields such as nuclear forensics and Stockpile Stewardship, accurate information about the energy dependence of neutron induced FPY are sparse, due primarily to the lack of suitable monoenergetic neutron sources. There is a clear need for improved data, and to address this issue, a collaboration was formed between Los Alamos National Laboratory (LANL), Lawrence Livermore National Laboratory (LLNL) and the Triangle Universities Nuclear Laboratory (TUNL) to measure the energy dependence of FPY for 235U, 238U and 239Pu. The measurements have been performed at TUNL, using a 10 MV Tandem Van de Graaff accelerator to produce monoenergetic neutrons at energies between 0.6 MeV to 14.8 MeV through a variety of reactions. The measurements have utilized a dual-fission chamber, with thin (10-100 μg/cm2) reference foils of similar material to a thick (100-400 mg) activation target held in the center between the chambers. This method allows for the accurate determination of the number of fissions that occurred in the thick target without requiring knowledge of the fission cross section or neutron fluence on target. Following activation, the thick target was removed from the dual-fission chamber and gamma

  19. Energy Dependence of Fission Product Yields from 235U, 238U and 239Pu for Incident Neutron Energies Between 0.5 and 14.8 MeV

    SciTech Connect

    Gooden, M. E.; Arnold, C. W.; Becker, J. A.; Bhatia, C.; Bhike, M.; Bond, E. M.; Bredeweg, T. A.; Fallin, B.; Fowler, M. M.; Howell, C. R.; Kelley, J. H.; Krishichayan,; Macri, R.; Rusev, G.; Ryan, C.; Sheets, S. A.; Stoyer, M. A.; Tonchev, A. P.; Tornow, W.; Vieira, D. J.; Wilhelmy, J. B.

    2016-01-01

    Fission Product Yields (FPY) have historically been one of the most observable features of the fission process. They are known to have strong variations that are dependent on the fissioning species, the excitation energy, and the angular momentum of the compound system. However, consistent and systematic studies of the variation of these FPY with energy have proved challenging. This is caused primarily by the nature of the experiments that have traditionally relied on radiochemical procedures to isolate specific fission products. Although radiochemical procedures exist that can isolate all products, each element presents specific challenges and introduces varying degrees of systematic errors that can make inter-comparison of FPY uncertain. Although of high importance in fields such as nuclear forensics and Stockpile Stewardship, accurate information about the energy dependence of neutron induced FPY are sparse, due primarily to the lack of suitable monoenergetic neutron sources. There is a clear need for improved data, and to address this issue, a collaboration was formed between Los Alamos National Laboratory (LANL), Lawrence Livermore National Laboratory (LLNL) and the Triangle Universities Nuclear Laboratory (TUNL) to measure the energy dependence of FPY for 235U, 238U and 239Pu. The measurements have been performed at TUNL, using a 10 MV Tandem Van de Graaff accelerator to produce monoenergetic neutrons at energies between 0.6 MeV to 14.8 MeV through a variety of reactions. The measurements have utilized a dual-fission chamber, with thin (10-100 μg/cm2) reference foils of similar material to a thick (100-400 mg) activation target held in the center between the chambers. This method allows for the accurate determination of the number of fissions that occurred in the thick target without requiring knowledge of the fission cross section or neutron fluence on target. Following activation, the thick target was removed

  20. Exploratory study of fission product yields of neutron-induced fission of U235, U238, and Pu239 at 8.9 MeV

    SciTech Connect

    Bhatia, C.; Fallin, B. F.; Gooden, M. E.; Howell, C. R.; Kelley, J. H.; Tornow, W.; Arnold, C. W.; Bond, E.; Bredeweg, T. A.; Fowler, M. M.; Moody, W.; Rundberg, R. S.; Rusev, G. Y.; Vieira, D. J.; Wilhelmy, J. B.; Becker, J. A.; Macri, R.; Ryan, C.; Sheets, S. A.; Stoyer, M. A.; Tonchev, A. P.

    2015-06-05

    Using dual-fission chambers each loaded with a thick (200–400–mg/cm2) actinide target of 235,238U or 239Pu and two thin (~10–100–μg/cm2) reference foils of the same actinide, the cumulative yields of fission products ranging from 92Sr to 147Nd have been measured at En = 8.9MeV. The 2H(d,n) 3He reaction provided the quasimonoenergetic neutron beam. Here, the experimental setup and methods used to determine the fission product yield (FPY) are described, and results for typically eight high-yield fission products are presented.