WorldWideScience

Sample records for actinide transmutation capability

  1. Transmutation of actinides in power reactors.

    Science.gov (United States)

    Bergelson, B R; Gerasimov, A S; Tikhomirov, G V

    2005-01-01

    Power reactors can be used for partial short-term transmutation of radwaste. This transmutation is beneficial in terms of subsequent storage conditions for spent fuel in long-term storage facilities. CANDU-type reactors can transmute the main minor actinides from two or three reactors of the VVER-1000 type. A VVER-1000-type reactor can operate in a self-service mode with transmutation of its own actinides.

  2. Actinide transmutation in nuclear reactors

    Energy Technology Data Exchange (ETDEWEB)

    Bultman, J.H.

    1995-01-17

    An optimization method is developed to maximize the burning capability of the ALMR while complying with all constraints imposed on the design for reliability and safety. This method leads to a maximal transuranics enrichment, which is being limited by constraints on reactivity. The enrichment can be raised by using the neutrons less efficiently by increasing leakage from the fuel. With the developed optimization method, a metallic and an oxide fueled ALMR were optimized. Both reactors perform equally well considering the burning of transuranics. However, metallic fuel has a much higher heat conductivity coefficient, which in general leads to better safety characteristics. In search of a more effective waste transmuter, a modified Molten Salt Reactor was designed. A MSR operates on a liquid fuel salt which makes continuous refueling possible, eliminating the issue of the burnup reactivity loss. Also, a prompt negative reactivity feedback is possible for an overmoderated reactor design, even when the Doppler coefficient is positive, due to the fuel expansion with fuel temperature increase. Furthermore, the molten salt fuel can be reprocessed based on a reduction process which is not sensitive to the short-lived spontaneously fissioning actinides. (orig./HP).

  3. Transmuting minor actinides with thermal reactor neutrons

    Directory of Open Access Journals (Sweden)

    Yu. A Kazansky

    2015-11-01

    The final conclusion about the practicability of Americium and Curium transmutation must be drawn by taking into account in the considered scenarios the difference in probability of the environmental release, the difference of biological effect and the transmutation efficiency of minor actinides continuously fed to spent fuel storages by the operating nuclear energy industry.

  4. Actinide and fission product partitioning and transmutation

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-07-01

    The fourth international information exchange meeting on actinide and fission product partitioning and transmutation, took place in Mito City in Japan, on 111-13 September 1996. The proceedings are presented in six sessions: the major programmes and international cooperation, the partitioning and transmutation programs, feasibility studies, particular separation processes, the accelerator driven transmutation, and the chemistry of the fuel cycle. (A.L.B.)

  5. Actinide and fission product separation and transmutation

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1993-07-01

    The second international information exchange meeting on actinide and fission product separation and transmutation, took place in Argonne National Laboratory in Illinois United States, on 11-13 November 1992. The proceedings are presented in four sessions: Current strategic system of actinide and fission product separation and transmutation, progress in R and D on partitioning processes wet and dry, progress in R and D on transmutation and refinements of neutronic and other data, development of the fuel cycle processes fuel types and targets. (A.L.B.)

  6. Actinide and fission product partitioning and transmutation

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-07-01

    The third international information exchange meeting on actinide and fission product partitioning and transmutation, took place in Cadarache France, on 12-14 December 1994. The proceedings are presented in six sessions : an introduction session, the major programmes and international cooperation, the systems studies, the reactors fuels and targets, the chemistry and a last discussions session. (A.L.B.)

  7. Actinide and fission product separation and transmutation

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1991-07-01

    The first international information exchange meeting on actinide and fission product separation and transmutation, took place in Mito in Japan, on 6-8 November 1990. It starts with a number of general overview papers to give us some broad perspectives. Following that it takes a look at some basic facts about physics and about the quantities of materials it is talking about. Then it proceeds to some specific aspects of partitioning, starting with evolution from today commercially applied processes and going on to other possibilities. At the end of the third session it takes a look at the significance of partitioning and transmutation of actinides before it embarks on two sessions on transmutation, first in reactors and second in accelerators. The last session is designed to throw back into the discussion the main points which need to be looked at when considering future work in this area. (A.L.B.)

  8. Scenarios for the transmutation of actinides in CANDU reactors

    Energy Technology Data Exchange (ETDEWEB)

    Hyland, Bronwyn, E-mail: hylandb@aecl.ca [Atomic Energy of Canada Limited, Chalk River Laboratories, Chalk River, Ontario, K0J 1J0 (Canada); Gihm, Brian, E-mail: gihmb@aecl.ca [Atomic Energy of Canada Limited, 2251 Speakman Drive, Mississauga, Ontario, L5K 1B2 (Canada)

    2011-12-15

    With world stockpiles of used nuclear fuel increasing, the need to address the long-term utilization of this resource is being studied. Many of the transuranic (TRU) actinides in nuclear spent fuel produce decay heat for long durations, resulting in significant nuclear waste management challenges. These actinides can be transmuted to shorter-lived isotopes to reduce the decay heat period or consumed as fuel in a CANDU(R) reactor. Many of the design features of the CANDU reactor make it uniquely adaptable to actinide transmutation. The small, simple fuel bundle simplifies the fabrication and handling of active fuels. Online refuelling allows precise management of core reactivity and separate insertion of the actinides and fuel bundles into the core. The high neutron economy of the CANDU reactor results in high TRU destruction to fissile-loading ratio. This paper provides a summary of actinide transmutation schemes that have been studied in CANDU reactors at AECL, including the works performed in the past. The schemes studied include homogeneous scenarios in which actinides are uniformly distributed in all fuel bundles in the reactor, as well as heterogeneous scenarios in which dedicated channels in the reactor are loaded with actinide targets and the rest of the reactor is loaded with fuel. The transmutation schemes that are presented reflect several different partitioning schemes. Separation of americium, often with curium, from the other actinides enables targeted destruction of americium, which is a main contributor to the decay heat 100-1000 years after discharge from the reactor. Another scheme is group-extracted transuranic elements, in which all of the transuranic elements, plutonium (Pu), neptunium (Np), americium (Am), and curium (Cm) are extracted together and then transmuted. This paper also addresses ways of utilizing the recycled uranium, another stream from the separation of spent nuclear fuel, in order to drive the transmutation of other actinides.

  9. Development of Metallic Fuels for Actinide Transmutation

    Energy Technology Data Exchange (ETDEWEB)

    Hayes, Steven Lowe [Idaho National Laboratory; Fielding, Randall Sidney [Idaho National Laboratory; Benson, Michael Timothy [Idaho National Laboratory; Chichester, Heather Jean MacLean [Idaho National Laboratory; Carmack, William Jonathan [Idaho National Laboratory

    2015-09-01

    Research and development activities on metallic fuels are focused on their potential use for actinide transmutation in future sodium fast reactors. As part of this application, there is also a need for a near zero-loss fabrication process and a desire to demonstrate a multifold increase in burnup potential. The incorporation of Am and Np into the traditional U-20Pu-10Zr metallic fuel alloy was demonstrated in the US during the Integral Fast Reactor Program of the 1980’s and early 1990’s. However, the conventional counter gravity injection casting method performed under vacuum, previously used to fabricate these metallic fuel alloys, was not optimized for mitigating loss of the volatile Am constituent in the casting charge; as a result, approximately 40% of the Am casting charge failed to be incorporated into the as-cast fuel alloys. Fabrication development efforts of the past few years have pursued an optimized bottom-pour casting method to increase utilization of the melted charge to near 100%, and a differential pressure casting approach, performed under an argon overpressure, has been demonstrated to result in essentially no loss of Am due to volatilization during fabrication. In short, a path toward zero-loss fabrication of metallic fuels including minor actinides has been shown to be feasible. Irradiation testing of advanced metallic fuel alloys in the Advanced Test Reactor (ATR) has been underway since 2003. Testing in the ATR is performed inside of cadmium-shrouded positions to remove >99% of the thermal flux incident on the test fuels, resulting in an epi-thermal driven fuel test that is free from gross flux depression and producing an essentially prototypic radial temperature profile inside the fuel rodlets. To date, three irradiation test series (AFC-1,2,3) have been completed. Over 20 different metallic fuel alloys have been tested to burnups as high as 30% with constituent compositions of Pu up to 30%, Am up to 12%, Np up to 10%, and Zr between 10

  10. Analysis of the Gas Core Actinide Transmutation Reactor (GCATR)

    Science.gov (United States)

    Clement, J. D.; Rust, J. H.

    1977-01-01

    Design power plant studies were carried out for two applications of the plasma core reactor: (1) As a breeder reactor, (2) As a reactor able to transmute actinides effectively. In addition to the above applications the reactor produced electrical power with a high efficiency. A reactor subsystem was designed for each of the two applications. For the breeder reactor, neutronics calculations were carried out for a U-233 plasma core with a molten salt breeding blanket. A reactor was designed with a low critical mass (less than a few hundred kilograms U-233) and a breeding ratio of 1.01. The plasma core actinide transmutation reactor was designed to transmute the nuclear waste from conventional LWR's. The spent fuel is reprocessed during which 100% of Np, Am, Cm, and higher actinides are separated from the other components. These actinides are then manufactured as oxides into zirconium clad fuel rods and charged as fuel assemblies in the reflector region of the plasma core actinide transmutation reactor. In the equilibrium cycle, about 7% of the actinides are directly fissioned away, while about 31% are removed by reprocessing.

  11. Actinide Partitioning and Transmutation Program. Progress report, April 1--June 30, 1977

    Energy Technology Data Exchange (ETDEWEB)

    Tedder, D. W.; Blomeke, J. O. [comps.

    1977-10-01

    Experimental work on the 16 tasks comprising the Actinide Partitioning and Transmutation Program was continued. Summaries of work are given on Purex Process modifications, actinide recovery, Am-Cm recovery, radiation effects on ion exchangers, LMFBR transmutation studies, thermal reactor transmutation studies, fuel cycle studies, and partitioning-transmutation evaluation. (JRD)

  12. Actinide partitioning-transmutation program final report. I. Overall assessment

    Energy Technology Data Exchange (ETDEWEB)

    Croff, A.G.; Blomeke, J.O.; Finney, B.C.

    1980-06-01

    This report is concerned with an overall assessment of the feasibility of and incentives for partitioning (recovering) long-lived nuclides from fuel reprocessing and fuel refabrication plant radioactive wastes and transmuting them to shorter-lived or stable nuclides by neutron irradiation. The principal class of nuclides considered is the actinides, although a brief analysis is given of the partitioning and transmutation (P-T) of /sup 99/Tc and /sup 129/I. The results obtained in this program permit us to make a comparison of the impacts of waste management with and without actinide recovery and transmutation. Three major conclusions concerning technical feasibility can be drawn from the assessment: (1) actinide P-T is feasible, subject to the acceptability of fuels containing recycle actinides; (2) technetium P-T is feasible if satisfactory partitioning processes can be developed and satisfactory fuels identified (no studies have been made in this area); and (3) iodine P-T is marginally feasible at best because of the low transmutation rates, the high volatility, and the corrosiveness of iodine and iodine compounds. It was concluded on the basis of a very conservative repository risk analysis that there are no safety or cost incentives for actinide P-T. In fact, if nonradiological risks are included, the short-term risks of P-T exceed the long-term benefits integrated over a period of 1 million years. Incentives for technetium and iodine P-T exist only if extremely conservative long-term risk analyses are used. Further RD and D in support of P-T is not warranted.

  13. Actinides transmutation - a comparison of results for PWR benchmark

    Energy Technology Data Exchange (ETDEWEB)

    Claro, Luiz H. [Instituto de Estudos Avancados (IEAv/CTA), Sao Jose dos Campos, SP (Brazil)], e-mail: luizhenu@ieav.cta.br

    2009-07-01

    The physical aspects involved in the Partitioning and Transmutation (P and T) of minor actinides (MA) and fission products (FP) generated by reactors PWR are of great interest in the nuclear industry. Besides these the reduction in the storage of radioactive wastes are related with the acceptability of the nuclear electric power. From the several concepts for partitioning and transmutation suggested in literature, one of them involves PWR reactors to burn the fuel containing plutonium and minor actinides reprocessed of UO{sub 2} used in previous stages. In this work are presented the results of the calculations of a benchmark in P and T carried with WIMSD5B program using its new cross sections library generated from the ENDF-B-VII and the comparison with the results published in literature by other calculations. For comparison, was used the benchmark transmutation concept based in a typical PWR cell and the analyzed results were the k{infinity} and the atomic density of the isotopes Np-239, Pu-241, Pu-242 and Am-242m, as function of burnup considering discharge of 50 GWd/tHM. (author)

  14. Helium and fission gas behaviour in magnesium aluminate spinel and zirconia for actinide transmutation

    NARCIS (Netherlands)

    Damen, P.M.G.

    2003-01-01

    In order to reduce the long-term radiotoxicity of spent nuclear fuel, many studies are performed on partitioning and transmutation of actinides. In such a scenario, the long-lived radio-isotopes (mostly actinides) are partitioned from the nuclear waste, and subsequently transmuted or fissioned in a

  15. Helium and fission gas behaviour in magnesium aluminate spinel and zirconia for actinide transmutation

    NARCIS (Netherlands)

    Damen, P.M.G.

    2003-01-01

    In order to reduce the long-term radiotoxicity of spent nuclear fuel, many studies are performed on partitioning and transmutation of actinides. In such a scenario, the long-lived radio-isotopes (mostly actinides) are partitioned from the nuclear waste, and subsequently transmuted or fissioned in a

  16. Fabrication of nitride fuels for transmutation of minor actinides

    Science.gov (United States)

    Minato, Kazuo; Akabori, Mitsuo; Takano, Masahide; Arai, Yasuo; Nakajima, Kunihisa; Itoh, Akinori; Ogawa, Toru

    2003-07-01

    At the Japan Atomic Energy Research Institute, the concept of the transmutation of minor actinides (MA: Np, Am and Cm) with accelerator-driven systems is being studied. The MA nitride fuel has been chosen as a candidate because of the possible mutual solubility among the actinide mononitrides and excellent thermal properties besides supporting hard neutron spectrum. MA nitrides of NpN, (Np, Pu)N, (Np, U)N, AmN, (Am, Y)N, (Am, Zr)N and (Cm, Pu)N were prepared from the oxides by the carbothermic reduction method. The prepared MA nitrides were examined by X-ray diffraction and the contents of impurities of oxygen and carbon were measured. The fabrication conditions for MA nitrides were improved so as to reduce the impurity contents. For an irradiation test of U-free nitride fuels, pellets of (Pu, Zr)N and PuN + TiN were prepared and a He-bonded fuel pin was fabricated. The irradiation test started in May 2002 and will go on for two years in the Japan Materials Testing Reactor.

  17. Sensitivity analysis of minor actinides transmutation to physical and technological parameters

    Directory of Open Access Journals (Sweden)

    Kooyman Timothée

    2015-01-01

    Full Text Available Minor actinides transmutation is one of the three main axis defined by the 2006 French law for management of nuclear waste, along with long-term storage and use of a deep geological repository. Transmutation options for critical systems can be divided in two different approaches: (a homogeneous transmutation, in which minor actinides are mixed with the fuel. This exhibits the drawback of “polluting” the entire fuel cycle with minor actinides and also has an important impact on core reactivity coefficients such as Doppler Effect or sodium void worth for fast reactors when the minor actinides fraction increases above 3 to 5% depending on the core; (b heterogeneous transmutation, in which minor actinides are inserted into transmutation targets which can be located in the center or in the periphery of the core. This presents the advantage of decoupling the management of the minor actinides from the conventional fuel and not impacting the core reactivity coefficients. In both cases, the design and analyses of potential transmutation systems have been carried out in the frame of Gen IV fast reactor using a “perturbation” approach in which nominal power reactor parameters are modified to accommodate the loading of minor actinides. However, when designing such a transmutation strategy, parameters from all steps of the fuel cycle must be taken into account, such as spent fuel heat load, gamma or neutron sources or fabrication feasibility. Considering a multi-recycling strategy of minor actinides, an analysis of relevant estimators necessary to fully analyze a transmutation strategy has been performed in this work and a sensitivity analysis of these estimators to a broad choice of reactors and fuel cycle parameters has been carried out. No threshold or percolation effects were observed. Saturation of transmutation rate with regards to several parameters has been observed, namely the minor actinides volume fraction and the irradiation time

  18. Transmutation of nuclear waste. Status report RAS programme 1994: Recycling and transmutation of actinides and fission products

    Energy Technology Data Exchange (ETDEWEB)

    Cordfunke, E.H.P.; Gruppelaar, H.; Franken, W.M.P.

    1995-07-01

    This report describes the status and progress of the Dutch RAS programme on `Recycling and Transmutation of Actinides and Fission Products` over the year 1994, which is the first year of the second 4-year programme. This programme is outlined and a short progress report is given over 1994, including a listing of 23 reports and publications over the year 1994. Highlights of 1994 were: The completion of long-lived fission-product transmutation studies, the initiation of small-scale demonstration experiments in the HFR on Tc and I, the issue of reports on the potential of the ALMR (Advanced Liquid Metal Reactor) for transmutation adn the participation and international cooperation on irradiation experiments with actinides in inert matrices. The remaining chapters contain more extended contributions on recent developments and selected topics, under the headings: Benefits and risks of partitioning and transmutation, Perspective of chemical partitioning, Inert matrices, Evolutionary options (MOX), Perspective of heavy water reactors, Perspective of fast burners, Perspective of accelerator-based systems, Thorium cycle, Fission-product transmutation, End scenarios, and Executive summary and recommendations. (orig.).

  19. Optimisation of composite metallic fuel for minor actinide transmutation in an accelerator-driven system

    Science.gov (United States)

    Uyttenhove, W.; Sobolev, V.; Maschek, W.

    2011-09-01

    A potential option for neutralization of minor actinides (MA) accumulated in spent nuclear fuel of light water reactors (LWRs) is their transmutation in dedicated accelerator-driven systems (ADS). A promising fuel candidate dedicated to MA transmutation is a CERMET composite with Mo metal matrix and (Pu, Np, Am, Cm)O 2-x fuel particles. Results of optimisation studies of the CERMET fuel targeting to increasing the MA transmutation efficiency of the EFIT (European Facility for Industrial Transmutation) core are presented. In the adopted strategy of MA burning the plutonium (Pu) balance of the core is minimized, allowing a reduction in the reactivity swing and the peak power form-factor deviation and an extension of the cycle duration. The MA/Pu ratio is used as a variable for the fuel optimisation studies. The efficiency of MA transmutation is close to the foreseen theoretical value of 42 kg TW -1 h -1 when level of Pu in the actinide mixture is about 40 wt.%. The obtained results are compared with the reference case of the EFIT core loaded with the composite CERCER fuel, where fuel particles are incorporated in a ceramic magnesia matrix. The results of this study offer additional information for the EFIT fuel selection.

  20. Target fuels for plutonium and minor actinide transmutation in pressurized water reactors

    Energy Technology Data Exchange (ETDEWEB)

    Washington, J., E-mail: jwashing@gmail.com [Nuclear Science and Engineering Program, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); King, J., E-mail: kingjc@mines.edu [Nuclear Science and Engineering Program, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States); Shayer, Z., E-mail: zshayer@mines.edu [Department of Physics, Colorado School of Mines, 1500 Illinois St., Golden, CO 80401 (United States)

    2017-03-15

    Highlights: • We evaluate transmutation fuels for plutonium and minor actinide destruction in LWRs. • We model a modified AP1000 fuel assembly in SCALE6.1. • We evaluate spectral shift absorber coatings to improve transmutation performance. - Abstract: The average nuclear power plant produces twenty metric tons of used nuclear fuel per year, containing approximately 95 wt% uranium, 1 wt% plutonium, and 4 wt% fission products and transuranic elements. Fast reactors are a preferred option for the transmutation of plutonium and minor actinides; however, an optimistic deployment time of at least 20 years indicates a need for a nearer-term solution. This study considers a method for plutonium and minor actinide transmutation in existing light water reactors and evaluates a variety of transmutation fuels to provide a common basis for comparison and to determine if any single target fuel provides superior transmutation properties. A model developed using the NEWT module in the SCALE 6.1 code package provided performance data for the burnup of the target fuel rods in the present study. The target fuels (MOX, PuO{sub 2}, Pu{sub 3}Si{sub 2}, PuN, PuUZrH, PuZrH, PuZrHTh, and PuZrO{sub 2}) are evaluated over a 1400 Effective Full Power Days (EFPD) interval to ensure each assembly remained critical over the entire burnup period. The MOX (5 wt% PuO{sub 2}), Pu{sub 0.31}ZrH{sub 1.6}Th{sub 1.08}, and PuZrO{sub 2}MgO (8 wt% Pu) fuels result in the highest rate of plutonium transmutation with the lowest rate of curium-244 production. This study selected eleven different burnable absorbers (B{sub 4}C, CdO, Dy{sub 2}O{sub 3}, Er{sub 2}O{sub 3}, Eu{sub 2}O{sub 3}, Gd{sub 2}O{sub 3}, HfO{sub 2}, In{sub 2}O{sub 3}, Lu{sub 2}O{sub 3}, Sm{sub 2}O{sub 3}, and TaC) for evaluation as spectral shift absorber coatings on the outside of the fuel pellets to determine if an absorber coating can improve the transmutation properties of the target fuels. The PuZrO{sub 2}MgO (8 wt% Pu) target

  1. Detailed studies of Minor Actinide transmutation-incineration in high-intensity neutron fluxes

    Energy Technology Data Exchange (ETDEWEB)

    Bringer, O. [CEA/Saclay/DSM/DAPNIA, Gif-sur-Yvette (France); Al Mahamid, I. [Lawrence Berkeley National Laboratory, E.H. and S. Div., CA (United States); Blandin, C. [CEA/Cadarache/DEN/DER/SPEX, Saint-Paul-lez-Durances (France); Chabod, S. [CEA/Saclay/DSM/DAPNIA, Gif-sur-Yvette (France); Chartier, F. [CEA/Cadarache/DEN/DPC/SECR, Gif-sur-Yvette (France); Dupont, E.; Fioni, G. [CEA/Saclay/DSM/DAPNIA, Gif-sur-Yvette (France); Isnard, H. [CEA/Cadarache/DEN/DPC/SECR, Gif-sur-Yvette (France); Letourneau, A.; Marie, F. [CEA/Saclay/DSM/DAPNIA, Gif-sur-Yvette (France); Mutti, P. [Institut Laue-Langevin, Grenoble (France); Oriol, L. [CEA/Cadarache/DEN/DER/SPEX, Saint-Paul-lez-Durances (France); Panebianco, S.; Veyssiere, C. [CEA/Saclay/DSM/DAPNIA, Gif-sur-Yvette (France)

    2006-07-01

    The Mini-INCA project is dedicated to the measurement of incineration-transmutation chains and potentials of minor actinides in high-intensity thermal neutron fluxes. In this context, new types of detectors and methods of analysis have been developed. The {sup 241}Am and {sup 232}Th transmutation-incineration chains have been studied and several capture and fission cross sections measured very precisely, showing some discrepancies with existing data or evaluated data. An impact study was made on different based-like GEN-IV reactors. It underlines the necessity to proceed to precise measurements for a large number of minor-actinides that contribute to these future incineration scenarios. (authors)

  2. Analysis and optimization of minor actinides transmutation blankets with regards to neutron and gamma sources

    Directory of Open Access Journals (Sweden)

    Kooyman Timothée

    2017-01-01

    Full Text Available Heterogeneous loading of minor actinides in radial blankets is a potential solution to implement minor actinides transmutation in fast reactors. However, to compensate for the lower flux level experienced by the blankets, the fraction of minor actinides to be loaded in the blankets must be increased to maintain acceptable performances. This severely increases the decay heat and neutron source of the blanket assemblies, both before and after irradiation, by more than an order of magnitude in the case of neutron source for instance. We propose here to implement an optimization methodology of the blankets design with regards to various parameters such as the local spectrum or the mass to be loaded, with the objective of minimizing the final neutron source of the spent assembly while maximizing the transmutation performances of the blankets. In a first stage, an analysis of the various contributors to long- and short-term neutron and gamma source is carried out whereas in a second stage, relevant estimators are designed for use in the effective optimization process, which is done in the last step. A comparison with core calculations is finally done for completeness and validation purposes. It is found that the use of a moderated spectrum in the blankets can be beneficial in terms of final neutron and gamma source without impacting minor actinides transmutation performances compared to more energetic spectrum that could be achieved using metallic fuel for instance. It is also confirmed that, if possible, the use of hydrides as moderating material in the blankets is a promising option to limit the total minor actinides inventory in the fuel cycle. If not, it appears that focus should be put upon an increased residence time for the blankets rather than an increase in the acceptable neutron source for handling and reprocessing.

  3. Georgia Institute of Technology research on the Gas Core Actinide Transmutation Reactor (GCATR)

    Science.gov (United States)

    Clement, J. D.; Rust, J. H.; Schneider, A.; Hohl, F.

    1976-01-01

    The program reviewed is a study of the feasibility, design, and optimization of the GCATR. The program is designed to take advantage of initial results and to continue work carried out on the Gas Core Breeder Reactor. The program complements NASA's program of developing UF6 fueled cavity reactors for power, nuclear pumped lasers, and other advanced technology applications. The program comprises: (1) General Studies--Parametric survey calculations performed to examine the effects of reactor spectrum and flux level on the actinide transmutation for GCATR conditions. The sensitivity of the results to neutron cross sections are to be assessed. Specifically, the parametric calculations of the actinide transmutation are to include the mass, isotope composition, fission and capture rates, reactivity effects, and neutron activity of recycled actinides. (2) GCATR Design Studies--This task is a major thrust of the proposed research program. Several subtasks are considered: optimization criteria studies of the blanket and fuel reprocessing, the actinide insertion and recirculation system, and the system integration. A brief review of the background of the GCATR and ongoing research is presented.

  4. Transmutation of minor actinides discharged from LMFBR spent fuel in a high power density fusion reactor

    Energy Technology Data Exchange (ETDEWEB)

    Uebeyli, Mustafa E-mail: mubeyli@gazi.edu.tr

    2004-12-01

    Significant amounts of nuclear wastes consisting of plutonium, minor actinides and long lived fission products are produced during the operation of commercial nuclear power plants. Therefore, the destruction of these wastes is very important with respect to public health, environment and also the future of nuclear energy. In this study, transmutation of minor actinides (MAs) discharged from LMFBR spent fuel in a high power density fusion reactor has been investigated under a neutron wall load of 10 MW/m{sup 2} for an operation period of 10 years. Also, the effect of MA percentage on the transmutation has been examined. The fuel zone, containing MAs as spheres cladded with W-5Re, has been located behind the first wall to utilize the high neutron flux for transmutation effectively. Helium at 40 atm has been used as an energy carrier. At the end of the operation period, the total burning and transmutation are greater than the total buildups in all investigated cases, and very high burnups (420-470 GWd/tHM) are reached, depending on the MA content. The total transmutation rate values are 906 and 979 kg/GW{sub th} year at startup and decrease to 140 and 178 kg/GW{sub th} year at the end of the operation for fuel with 10% and 20% MA, respectively. Over an operation period of 10 years, the effective half lives decrease from 2.38, 2.21 and 3.08 years to 1.95, 1.80 and 2.59 years for {sup 237}Np, {sup 241}Am and {sup 243}Am, respectively. Total atomic densities decrease exponentially during the operation period. The reductions in the total atomic densities with respect to the initial ones are 79%, 81%, 82%, 83%, 85% and 86% for 10%, 12%, 14%, 16%, 18% and 20% MAs, respectively.

  5. Advances in fuel materials for the transmutation of actinides

    Energy Technology Data Exchange (ETDEWEB)

    Prunier, C.

    1994-12-31

    The physical feasibility of actinides, spent fuels and fission products burning in fission reactors is well understood. In fast reactors, this operation is more favourable. The homogeneous recycling mode has had a preliminary validation in Phenix (the Super fact experiment). For the heterogenous recycling mode, past experience for {sup 238} Pu production in thermal spectrum was obtained with Np O{sub 2}-Mg O targets. An irradiation experiment in Phenix blanket is foreseen with the same type of target. The {sup 237} Np problem seems to be most conveniently treated, even in the short term, by homogeneous recycling with Pu in fast reactors. (author). 15 figs., 4 tabs.

  6. Moderating Material to Compensate the Drawback of High Minor Actinide Containing Transmutation Fuel on the Feedback Effects in SFR Cores

    Directory of Open Access Journals (Sweden)

    Bruno Merk

    2013-01-01

    Full Text Available The use of fine distributed moderating material to enhance the feedback effects and to reduce the sodium void effecting SFRs is described. The drawback on the feedback effects due to the introduction of minor actinides into SFR fuel is analyzed. The possibility of compensation of the effect of the minor actinides on the feedback effects by the use of fine distributed moderating material is demonstrated. The consequences of the introduction of fine distributed moderating material into fuel assemblies with fuel configurations foreseen for minor actinide transmutation are analyzed, and the positive effects on the transmutation efficiency are shown. Finally, the possible increase of the Americium content to improve the transmutation efficiency is discussed, the limit value of Americium is determined, and the possibilities given by an increase of the hydrogen content are analyzed.

  7. The optimization of an AP1000 fuel assembly for the transmutation of plutonium and minor actinides

    Science.gov (United States)

    Washington, Jeremy A.

    The average nuclear power plant produces twenty metric tons of used nuclear fuel per year, containing approximately 95 wt% uranium, 1 wt% plutonium, and 4 wt% fission products and transuranic elements. Fast reactors are a preferred option for the transmutation of plutonium and minor actinides; however, an optimistic deployment time of at least 20 years indicates a need for a near-term solution. The goal of this thesis is to examine the potential of light water reactors for plutonium and minor actinides transmutation as a near-term solution. This thesis screens the available nuclear isotope database to identify potential absorbers as coatings on a transmutation fuel in a light water reactor. A spectral shift absorber coating tunes the neutron energy spectrum experienced by the underlying target fuel. Eleven different spectral shift absorbers (B4C, CdO, Dy2O3, Er 2O3, Eu2O3, Gd2O3, HfO2, In2O3, Lu2O3, Sm2O3, and TaC) have been selected for further evaluation. A model developed using the NEWT module of SCALE 6.1 code provided performance data for the burnup of the target fuel rods. Irradiation of the target fuels occurs in a Westinghouse 17x17 XL Robust Fuel Assembly over a 1400 Effective Full Power Days (EFPD) interval. The fuels evaluated in this thesis include PuO2, Pu3Si2, PuN, MOX, PuZrH, PuZrHTh, PuZrO 2, and PuUZrH. MOX (5 wt% PuO2), Pu0.31ZrH 1.6Th1.08, and PuZrO2MgO (8 wt%) are selected for detailed analysis in a multi-pin transmutation assembly. A coupled model optimized the resulting transmutation fuel elements. The optimization considered three stages of fuel assemblies containing target fuel pins. The first stage optimized four target fuel pins adjacent to the central instrumentation channel. The second stage evaluated a variety of assemblies with multiple target fuel pins and the third stage re-optimized target fuel pins in the second-stage assembly. A PuZrO2MgO (8 wt%) target fuel with a coating of Lu 2O3 resulted in the greatest reduction in curium-244

  8. Assessment of SFR fuel pin performance codes under advanced fuel for minor actinide transmutation

    Energy Technology Data Exchange (ETDEWEB)

    Bouineau, V.; Lainet, M.; Chauvin, N.; Pelletier, M. [French Alternative Energies and Atomic Energy Commission - CEA, CEA Cadarache, DEN/DEC/SESC, 13108 Saint Paul lez Durance (France); Di Marcello, V.; Van Uffelen, P.; Walker, C. [European Commission, Joint Research Centre, Institute for Transuranium Elements, Hermann-von-Helmholtz-Platz 1, D- 76344 Eggenstein-Leopoldshafen (Germany)

    2013-07-01

    Americium is a strong contributor to the long term radiotoxicity of high activity nuclear waste. Transmutation by irradiation in nuclear reactors of long-lived nuclides like {sup 241}Am is, therefore, an option for the reduction of radiotoxicity and residual power packages as well as the repository area. In the SUPERFACT Experiment four different oxide fuels containing high and low concentrations of {sup 237}Np and {sup 241}Am, representing the homogeneous and heterogeneous in-pile recycling concepts, were irradiated in the PHENIX reactor. The behavior of advanced fuel materials with minor actinide needs to be fully characterized, understood and modeled in order to optimize the design of this kind of fuel elements and to evaluate its performances. This paper assesses the current predictability of fuel performance codes TRANSURANUS and GERMINAL V2 on the basis of post irradiation examinations of the SUPERFACT experiment for pins with low minor actinide content. Their predictions have been compared to measured data in terms of geometrical changes of fuel and cladding, fission gases behavior and actinide and fission product distributions. The results are in good agreement with the experimental results, although improvements are also pointed out for further studies, especially if larger content of minor actinide will be taken into account in the codes. (authors)

  9. Actinide partitioning and transmutation program. Progress report, July 1--September 30, 1977

    Energy Technology Data Exchange (ETDEWEB)

    Tedder, D.W.; Blomeke, J.O. (comps.)

    1978-02-01

    In Purex process modifications, two cold runs with mixer-settlers were made on the extraction and stripping of ruthenium and zirconium without the presence of uranium. Efforts in actinide recovery from solids were directed toward the determination of dissolution parameters in various reagents for /sup 241/Am and /sup 239/Pu oxide mixtures, /sup 233/U oxide, /sup 237/Np oxide, /sup 244/Cm oxide, /sup 232/Th oxide, and PuO/sub 2/. Studies in americium-curium recovery with OPIX (oxalate precipitation and ion exchange), Talspeak, and cation exchange chromatography focused on the feasibility of forming oxalate precipitates in continuous systems, the effects of zirconium on Talspeak, and methods for removing solvent degradation products of the Talspeak system. In studies of americium-curium recovery using bidentate extractants, additional distribution coefficients for actinides and other key elements between reduced synthetic LWR waste solution and 30 percent dihexyl-N, N-diethyl-carbamylmethylene phosphonate in diisopropylbenzene were measured. Studies in the americium-curium recovery using inorganic ion exchange media to determine the pH dependence of lanthanide ion affinity for niobate, titanate, and zirconate ion exchange materials have been completed. A modified flowsheet for the extraction of uranium, neptunium, plutonium, americium, and curium from high-level liquid waste is presented. Evaluation of methods for measuring actinides from incinerator ash is continuing. A preliminary evaluation of methods for treatment of salt waste and waste waters was completed. In thermal reactor transmutation studies, waste actinides from an LWR lattice containing mixed uranium-plutonium assemblies were recycled in separate target assemblies. (LK)

  10. Actinide partitioning-transmutation program final report. IV. Miscellaneous aspects. [Transport; fuel fabrication; decay; policy; economics

    Energy Technology Data Exchange (ETDEWEB)

    Alexander, C.W.; Croff, A.G.

    1980-09-01

    This report discusses seven aspects of actinide partitioning-transmutation (P-T) which are important in any complete evaluation of this waste treatment option but which do not fall within other major topical areas concerning P-T. The so-called miscellaneous aspects considered are (1) the conceptual design of a shipping cask for highly neutron-active fresh and spent P-T fuels, (2) the possible impacts of P-T on mixed-oxide fuel fabrication, (3) alternatives for handling the existing and to-be-produced spent fuel and/or wastes until implementation of P-T, (4) the decay and dose characteristics of P-T and standard reactor fuels, (5) the implications of P-T on currently existing nuclear policy in the United States, (6) the summary costs of P-T, and (7) methods for comparing the risks, costs, and benefits of P-T.

  11. Effect of spectral characterization of gaseous fuel reactors on transmutation and burning of actinides

    Energy Technology Data Exchange (ETDEWEB)

    Fung, C.; Anghaie, S. [Florida Univ., Wilmington, NC (United States)

    2007-07-01

    Gaseous Core Reactors (GCR) are fueled with stable uranium compounds in a reflected cavity. The spectral characteristics of neutrons in GCR systems could shift from one end of the spectrum to the other end by changing design parameters such as reflector material and thickness, uranium enrichment, and the average operational temperature and pressure. The rate of actinide generation, transmutation, and burnup is highly influenced by the average neutron energy in reactor core. In particular, the production rate and isotopic mix of plutonium are highly dependent on the neutron spectrum in the reactor. Other actinides of primary interest to this work are neptunium-237 and americium-241 due to their pivotal impact on high-level nuclear waste disposal. In all cavity reactors including GCR's, the reflector material and thickness are the most important design parameters in determining the core spectrum. The increase in the gaseous fuel pressure and enrichment results in relative shift of neutron population toward energies greater than 2 eV. Reflector materials considered in this study are beryllium oxide, lithium hydride, lithium deuteride, zirconium carbide, graphite, lead, and tungsten. Results of the study suggest that the beryllium oxide and tungsten reflected GCR systems set the lower (softest) and upper (hardest) limits of neutron spectra, respectively. The inventory of actinides with half-lives greater than 1000 years can be minimized by increasing neutron flux level in the reactor core. The higher the neutron flux, the lower the inventory of these actinides. The majority of the GCR designs maintained a flux level on the order of 10{sup 15} cm{sup -2}*s{sup -1} while the PWR flux is one order of magnitude lower. The inventory of the feeder isotopes to Np{sup 237} including U{sup 237}, Pu{sup 241}, and Am{sup 241} decreases with relative shift of neutron spectrum toward higher energies. This is due to increased resonance absorption in these isotopes due to higher

  12. Hardening neutron spectrum for advanced actinide transmutation experiments in the ATR.

    Science.gov (United States)

    Chang, G S; Ambrosek, R G

    2005-01-01

    The most effective method for transmuting long-lived isotopes contained in spent nuclear fuel into shorter-lived fission products is in a fast neutron spectrum reactor. In the absence of a fast test reactor in the United States, initial irradiation testing of candidate fuels can be performed in a thermal test reactor that has been modified to produce a test region with a hardened neutron spectrum. Such a test facility, with a spectrum similar but somewhat softer than that of the liquid-metal fast breeder reactor (LMFBR), has been constructed in the INEEL's Advanced Test Reactor (ATR). The radial fission power distribution of the actinide fuel pin, which is an important parameter in fission gas release modelling, needs to be accurately predicted and the hardened neutron spectrum in the ATR and the LMFBR fast neutron spectrum is compared. The comparison analyses in this study are performed using MCWO, a well-developed tool that couples the Monte Carlo transport code MCNP with the isotope depletion and build-up code ORIGEN-2. MCWO analysis yields time-dependent and neutron-spectrum-dependent minor actinide and Pu concentrations and detailed radial fission power profile calculations for a typical fast reactor (LMFBR) neutron spectrum and the hardened neutron spectrum test region in the ATR. The MCWO-calculated results indicate that the cadmium basket used in the advanced fuel test assembly in the ATR can effectively depress the linear heat generation rate in the experimental fuels and harden the neutron spectrum in the test region.

  13. Detailed investigation of neutron emitters in the transmutation of Minor Actinides

    Energy Technology Data Exchange (ETDEWEB)

    Letourneau, A.; Bringer, O.; Dupont, E.; Panebianco, S.; Veyssiere, Ch. [CEA/Saclay/DSM/IRFU - Gif-sur-Yvette (France); Al Mahamid, I. [Wadsworth Center, New York State Department of Health, Albany, NY 12201 (United States); Chartier, F. [CEA/Saclay/DEN/DPC/SECR - Gif-sur-Yvette (France); Mutti, P. [Institut Laue-Langevin, Grenoble (France); Oriol, L. [CEA/Cadarache/DEN/DER/SPEX - Saint-Paul-lez-Durances (France)

    2008-07-01

    The production of neutron emitters during the incineration process of minor actinides could be very penalizing for the reprocessing of the targets when transmuted in heterogeneous mode, either in dedicated systems (ADS) or in generation IV reactors. Therefore their production has to be carefully evaluated. The reliability of such evaluation really depends on nuclear data (capture and fission cross sections) and their accuracy. In this paper we present a work we have done to investigate the production of neutron emitters in the incineration of {sup 237}Np and {sup 241}Am targets in fast and thermal nuclear reactor concepts. The impact of nuclear data uncertainties on the production of those neutron-emitters was evaluated by sensitivity calculations. The reduction for some of these uncertainties in the thermal energy region was done by measuring more precisely the {sup 244}Cm(n,gamma){sup 245}Cm, {sup 245}Cm(n,f) and {sup 249}Cf(n,gamma){sup 250}Cf capture cross sections at the Laue-Langevin Institute (ILL). It amounts to (15.6+-2.4) b for the first one, (1923+-49) b for the second and (389+-10) b for the third one. (authors)

  14. Optimization of plutonium and minor actinide transmutation in an AP1000 fuel assembly via a genetic search algorithm

    Energy Technology Data Exchange (ETDEWEB)

    Washington, J., E-mail: jwashing@gmail.com; King, J., E-mail: kingjc@mines.edu

    2017-01-15

    Highlights: • We model a modified AP1000 fuel assembly in SCALE6.1. • We couple the NEWT module of SCALE to the MOGA module of DAKOTA. • Transmutation is optimized based on choice of coating and fuel. • Greatest transmutation achieved with PuZrO{sub 2}MgO fuel pins coated with Lu{sub 2}O{sub 3}. - Abstract: The average nuclear power plant produces twenty metric tons of used nuclear fuel per year, which contains approximately 95 wt% uranium, 1 wt% plutonium, and 4 wt% fission products and transuranic elements. Fast reactors are the preferred option for the transmutation of plutonium and minor actinides; however, an optimistic deployment time of at least 20 years indicates a need for a near-term solution. Previous simulation work demonstrated the potential to transmute transuranic elements in a modified light water reactor fuel pin. This study optimizes a quarter-assembly containing target fuels coated with spectral shift absorbers for the transmutation of plutonium and minor actinides in light water reactors. The spectral shift absorber coating on the target fuel pin tunes the neutron energy spectrum experienced by the target fuel. A coupled model developed using the NEWT module from SCALE 6.1 and a genetic algorithm module from the DAKOTA optimization toolbox provided performance data for the burnup of the target fuel pins in the present study. The optimization with the coupled NEWT/DAKOTA model proceeded in three stages. The first stage optimized a single-target fuel pin per quarter-assembly adjacent to the central instrumentation channel. The second stage evaluated a variety of quarter-assemblies with multiple target fuel pins from the first stage and the third stage re-optimized the pins in the optimal second stage quarter-assembly. An 8 wt% PuZrO{sub 2}MgO inert matrix fuel pin with a 1.44 mm radius and a 0.06 mm Lu{sub 2}O{sub 3} coating in a five target fuel pin per quarter-assembly configuration represents the optimal combination for the

  15. Transmutation of minor actinides in high and representative neutron fluxes: the mini-INCA and MEGAPIE projects

    Energy Technology Data Exchange (ETDEWEB)

    Letourneau, A.; Chabod, S.; Marie, F.; Ridikas, D.; Toussaint, J.C.; Veyssiere, C. [CEA/DSM/DAPNIA Saclay, Gif-sur-Yvette (France); Blandin, C. [CEA/DEN/DER/SPEX Cadarache - Saint-Paul-lez-Durances (France); Mutti, P. [Inst. Laue-Langevin, Grenoble (France)

    2003-07-01

    In the framework of nuclear waste transmutation studies, the Mini-INCA project has been initiated at CEA/DSM with objectives to determine optimal conditions for transmutation and incineration of minor actinides (MA) in high intensity neutron fluxes. Our experimental tools based on alpha- and gamma-spectroscopy of the samples and the development of micro fission chambers could gather either microscopic information on nuclear reactions (total or partial cross sections for neutron capture and/or fission reactions) or macroscopic information on transmutation and incineration potentials. Neutron capture cross sections of selected actinides ({sup 241}Am, {sup 242}Am, {sup 242}Pu, {sup 237}Np) have already been measured at ILL, showing some discrepancies when compared to evaluated data libraries but in overall good agreement with recent data. The studies and possibilities offer by the MEGAPIE project to assess neutronic performances of a 1 MW spallation target and the incineration of MA in a representative neutron flux of a spallation source are also discussed. (orig.)

  16. A Summary of Actinide Enrichment Technologies and Capability Gaps

    Energy Technology Data Exchange (ETDEWEB)

    Patton, Bradley D. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Robinson, Sharon M. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

    2017-01-01

    The evaluation performed in this study indicates that a new program is needed to efficiently provide a national actinide radioisotope enrichment capability to produce milligram-to-gram quantities of unique materials for user communities as summarized in Table 1. This program xiv should leverage past actinide enrichment, the recent advances in stable isotope enrichment, and assessments of the future requirements to cost effectively develop this capability while establishing an experience base for a new generation of researchers in this vital area. Preliminary evaluations indicate that an EMIS device would have the capability to meet the future needs of the user community for enriched actinides. The EMIS technology could be potentially coupled with other enrichment technologies, such as irradiation, as pre-enrichment and/or post-enrichment systems to increase the throughput, reduce losses of material, and/or reduce operational costs of the base EMIS system. Past actinide enrichment experience and advances in the EMIS technology applied in stable isotope separations should be leveraged with this new evaluation information to assist in the establishment of a domestic actinide radioisotope enrichment capability.

  17. Nuclear data uncertainty analysis on a minor actinide burner for transmuting spent fuel

    Energy Technology Data Exchange (ETDEWEB)

    Choi, Hangbok

    1998-08-01

    A comprehensive sensitivity and uncertainty analysis was performed on a 1200 MWt minor actinides burner designed for a low burnup reactivity swing, negative doppler coefficient, and low sodium void worth. Sensitivities of the performance parameters were generated using depletion perturbation methods for the constrained close fuel cycle of the reactor. The uncertainty analysis was performed using the sensitivity and covariance data taken from ENDF-B/V and other published sources. The uncertainty analysis of a liquid metal reactor for burning minor actinide has shown that uncertainties in the nuclear data of several key minor actinide isotopes can introduce large uncertainties in the predicted performance of the core. The relative uncertainties in the burnup swing, doppler coefficient, and void worth were conservatively estimated to be 180 %, 97 %, and 46 %, respectively. An analysis was performed to prioritize the minor actinide reactions for reducing the uncertainties. (author). 41 refs., 17 tabs., 1 fig.

  18. Transmutation of Minor Actinides in a Spherical Torus Tokamak Fusion Reactor

    Institute of Scientific and Technical Information of China (English)

    FENGKaiming; ZHANGGuoshu

    2002-01-01

    Fusion energy will be a long-term energy source. Great efforts have been devoted to fusion research in the past 50 years, and there is still a long way to go. Transmutation of high-level waste (HLW) utilizing D-T fusion neutrons is a good choice for an early application of fusion.

  19. Analyses in Support of Z-Pinch IFE and Actinide Transmutation - LLNL Progress Report for FY-06

    Energy Technology Data Exchange (ETDEWEB)

    Meier, W R; Moir, R W; Abbott, R

    2006-09-19

    This report documents results of LLNL's work in support of two studies being conducted by Sandia National Laboratories (SNL): the development of the Z-pinch driven inertial fusion energy (Z-IFE), and the use of Z-pinch driven inertial fusion as a neutron source to destroy actinides from fission reactor spent fuel. LLNL's efforts in FY06 included: (1) Development of a systems code for Z-IFE and use of the code to examine the operating parameter space in terms of design variables such as the Z-pinch driver energy, the chamber pulse repetition rate, the number of chambers making up the power plant, and the total net electric power of the plant. This is covered in Section 3 with full documentation of the model in Appendix A. (2) Continued development of innovative concepts for the design and operation of the recyclable transmission line (RTL) and chamber for Z-IFE. The work, which builds on our FY04 and FY05 contributions, emphasizes design features that are likely to lead to a more attractive power plant including: liquid jets to protect all structures from direct exposure to neutrons, rapid insertion of the RTL to maximize the potential chamber rep-rate, and use of cast flibe for the RTL to reduce recycling and remanufacturing costs and power needs. See Section 4 and Appendix B. (3) Description of potential figures of merit (FOMs) for actinide transmutation technologies and a discussion of how these FOMs apply and can be used in the ongoing evaluation of the Z-pinch actinide burner, referred to as the In-Zinerator. See Section 5. (4) A critique of, and suggested improvements to, the In-Zinerator chamber design in response to the SNL design team's request for feedback on its preliminary design. This is covered in Section 6.

  20. First results of the irradiation program of inert matrices, targets and fuels for minor actinides transmutation in fast reactor

    Energy Technology Data Exchange (ETDEWEB)

    Bonnerot, Jean-Marc; Ferroud-Plattet, Marie-Pierre; Lamontagne, Jerome [CEA Cadarache, Nuclear Energy Direction, Saint-Paul les Durance Cedex, 13108 (France); Warin, Dominique [CEA Valrho, Nuclear Energy Direction, DRCP, Bagnols-sur-Ceze Cedex, 30207 (France); Gosmain, Lionel [CEA Saclay, Nuclear Energy Direction, DMN, Gif sur Yvette, 91190 (France)

    2008-07-01

    A comprehensive irradiation program was started in France in 1992 to demonstrate the technical feasibility of the transmutation of minor actinides in current and future nuclear reactors, by means of inert support targets or dedicated fuels. The first step of the program (MATINA program) consisted in the irradiation of various inert materials intended as support matrix for transmutation targets, in the fast reactor Phenix, to select the best candidates. These inert materials included as well oxide and nitride ceramics - MgO, MgAl{sub 2}O{sub 4}, Al{sub 2}O{sub 3}, Y{sub 3}Al{sub 5}O{sub 12} and TiN - as refractory metals - W, Nb, Cr and V- and were irradiated under fast neutron flux at temperatures ranged between 650 and 1040 deg. C. The results show that in comparison to MgO, MgAl{sub 2}O{sub 4} and Al{sub 2}O{sub 3} inert matrices irradiated alone, the composite pellets containing UO{sub 2} particles, showed very different behaviors under irradiation. The swelling of MgO pellets is enhanced in the presence of fissile material whereas it is lowered for the Al{sub 2}O{sub 3}-UO{sub 2} pellets. MgAl{sub 2}O{sub 4}-UO{sub 2} pellets remained stable. The second step of the program aimed at testing the behavior of inert support targets containing americium. A new experiment ECRIX H involving composite pellets with an MgO matrix and AmO{sub 2-x} particles was performed in Phenix and completed in 2006. A rather low elongation of the pellet stack was observed and no significant diameter deformation of cladding was detected after irradiation. The analysis of the filling gas of the pin after puncturing, revealed that respectively 28% and 5% of the He and Xe+Kr created under irradiation were released in the expanding volume of the pin. ECRIX H, which is the first experiment on Am base target in Phenix, will undoubtedly represent a very important step in the general design approach about inert matrix support targets once the complete results should be available by the end of

  1. Measurements of the neutron capture cross sections and incineration potentials of minor-actinides in high thermal neutron fluxes: Impact on the transmutation of nuclear wastes; Mesures des sections efficaces de capture et potentiels d'incineration des actinides mineurs dans les hauts flux de neutrons: Impact sur la transmutation des dechets

    Energy Technology Data Exchange (ETDEWEB)

    Bringer, O

    2007-10-15

    This thesis comes within the framework of minor-actinide nuclear transmutation studies. First of all, we have evaluated the impact of minor actinide nuclear data uncertainties within the cases of {sup 241}Am and {sup 237}Np incineration in three different reactor spectra: EFR (fast), GT-MHR (epithermal) and HI-HWR (thermal). The nuclear parameters which give the highest uncertainties were thus highlighted. As a result of fact, we have tried to reduce data uncertainties, in the thermal energy region, for one part of them through experimental campaigns in the moderated high intensity neutron fluxes of ILL reactor (Grenoble). These measurements were focused onto the incineration and transmutation of the americium-241, the curium-244 and the californium-249 isotopes. Finally, the values of 12 different cross sections and the {sup 241}Am isomeric branching ratio were precisely measured at thermal energy point. (author)

  2. Sensitivity to Nuclear Data and Neutron Source Type in Calculations of Transmutation Capabilities of the Energy Amplifier Demonstration Facility

    Energy Technology Data Exchange (ETDEWEB)

    Dahlfors, Marcus

    2003-05-01

    This text is a summary of two studies the author has performed within the field of 3-D Monte Carlo calculations of Accelerator Driven Systems (ADS) for transmutation of nuclear waste. The simulations were carried out with the state-of-the-art computer code package EA-MC, developed by C. Rubbia and his group at CERN. The concept studied is ANSALDOs 80 MWth Energy Amplifier Demonstration Facility based on classical MOX-fuel technology and on molten Lead-Bismuth Eutectic cooling. A review of neutron cross section sensitivity in numerical calculations of an ADS and a comparative assessment relevant to the transmutation efficiency of plutonium and minor actinides in fusion/fission hybrids and ADS are presented.

  3. Actinide management with commercial fast reactors

    Energy Technology Data Exchange (ETDEWEB)

    Ohki, Shigeo [Japan Atomic Energy Agency, 4002, Narita-cho, O-arai-machi, Higashi-Ibaraki-gun, Ibaraki 311-1393 (Japan)

    2015-12-31

    The capability of plutonium-breeding and minor-actinide (MA) transmutation in the Japanese commercial sodium-cooled fast reactor offers one of practical solutions for obtaining sustainable energy resources as well as reducing radioactive toxicity and inventory. The reference core design meets the requirement of flexible breeding ratio from 1.03 to 1.2. The MA transmutation amount has been evaluated as 50-100 kg/GW{sub e}y if the MA content in fresh fuel is 3-5 wt%, where about 30-40% of initial MA can be transmuted in the discharged fuel.

  4. Actinide management with commercial fast reactors

    Science.gov (United States)

    Ohki, Shigeo

    2015-12-01

    The capability of plutonium-breeding and minor-actinide (MA) transmutation in the Japanese commercial sodium-cooled fast reactor offers one of practical solutions for obtaining sustainable energy resources as well as reducing radioactive toxicity and inventory. The reference core design meets the requirement of flexible breeding ratio from 1.03 to 1.2. The MA transmutation amount has been evaluated as 50-100 kg/GWey if the MA content in fresh fuel is 3-5 wt%, where about 30-40% of initial MA can be transmuted in the discharged fuel.

  5. Calculations of the actinide transmutation with HELIOS for fuels of light water reactors; Calculos de la transmutacion de actinidos con HELIOS para combustibles de reactores de agua ligera

    Energy Technology Data Exchange (ETDEWEB)

    Francois L, J.L.; Guzman A, J.R. [UNAM-FI, Laboratorio de Analisis en Ingenieria de Reactores Nucleares, Paseo Cuauhnahuac 8532, Jiutepec, Morelos (Mexico)]. e-mail: jlfl@fi-b.unam.mx

    2006-07-01

    In this work a comparison of the obtained results with the HELIOS code is made and those obtained by other similar codes, used in the international community, respect to the transmutation of smaller actinides. For this the one it is analyzed the international benchmark: 'Calculations of Different Transmutation Concepts', of the Nuclear Energy Agency. In this benchmark two cell types are analyzed: one small corresponding to a PWR standard, and another big one corresponding to a PWR highly moderated. Its are considered two types of burnt of discharge: 33 GWd/tHM and 50 GWd/tHM. The following types of results are approached: the k{sub eff} like a function of the burnt one, the atomic densities of the main isotopes of the actinides, the radioactivities in the moment in that the reactor it is off and in the times of cooling from 7 up to 50000 years, the reactivity by holes and the Doppler reactivity. The results are compared with those obtained by the following institutions: FZK (Germany), JAERI (Japan), ITEP (Russia) and IPPE (Russian Federation). In the case of the eigenvalue, the obtained results with HELIOS showed a discrepancy around 3% {delta}k/k, which was also among other participants. For the isotopic concentrations: {sup 241}Pu, {sup 242} Pu and {sup 242m} Am the results of all the institutions present a discrepancy bigger every time, as the burnt one increases. Regarding the activities, the discrepancy of results is acceptable, except in the case of the {sup 241} Pu. In the case of the Doppler coefficients the discrepancy of results is acceptable, except for the cells with high moderation; in the case of the holes coefficients, the discrepancy of results increases in agreement with the holes fraction increases, being quite high to 95% of holes. In general, the results are consistent and in good agreement with those obtained by all the participants in the benchmark. The results are inside of the established limits by the work group on Plutonium Fuels

  6. Heavy ion induced damage in MgAl sub 2 O sub 4 , an inert matrix candidate for the transmutation of minor actinides

    CERN Document Server

    Wiss, T

    1999-01-01

    Magnesium aluminum spinel (MgAl sub 2 O sub 4) is a material selected as a possible matrix for transmutation of minor actinides by neutron capture or fission in nuclear reactors. To study the radiation stability of this inert matrix, especially against fission product impact, irradiations with heavy energetic ions or clusters have been performed. The high electronic energy losses of the heavy ions in this material led to the formation of visible tracks as evidenced by transmission electron microscopy for 30 MeV C sub 6 sub 0 -Buckminster fullerenes and for ions of energy close to or higher than fission energy ( sup 2 sup 0 sup 9 Bi with 120 MeV and 2.38 GeV energy). The irradiations at high energies showed a pronounced degradation of the spinel. Additionally, MgAl sub 2 O sub 4 exhibited a large swelling for irradiation at high fluences with fission products of fission energy (here I-ions of 72 MeV) and at temperatures <= 500 deg. C. These observations are discussed from the technological point of view in ...

  7. Calculation and Analysis of B/T (Burning and/or Transmutation Rate of Minor Actinides and Plutonium Performed by Fast B/T Reactor

    Directory of Open Access Journals (Sweden)

    Marsodi

    2006-01-01

    Full Text Available Calculation and analysis of B/T (Burning and/or Transmutation rate of MA (minor actinides and Pu (Plutonium has been performed in fast B/T reactor. The study was based on the assumption that the spectrum shift of neutron flux to higher side of neutron energy had a potential significance for designing the fast B/T reactor and a remarkable effect for increasing the B/T rate of MA and/or Pu. The spectrum shifts of neutron have been performed by change MOX to metallic fuel. Blending fraction of MA and or Pu in B/T fuel and the volume ratio of fuel to coolant in the reactor core were also considered. Here, the performance of fast B/T reactor was evaluated theoretically based on the calculation results of the neutronics and burn-up analysis. In this study, the B/T rate of MA and/or Pu increased by increasing the blending fraction of MA and or Pu and by changing the F/C ratio. According to the results, the total B/T rate, i.e. [B/T rate]MA + [B/T rate]Pu, could be kept nearly constant under the critical condition, if the sum of the MA and Pu inventory in the core is nearly constant. The effect of loading structure was examined for inner or outer loading of concentric geometry and for homogeneous loading. Homogeneous loading of B/T fuel was the good structure for obtaining the higher B/T rate, rather than inner or outer loading

  8. Set up of an innovative methodology to measure on-line the incineration potential of minor actinides under very high neutron sources in the frame of the future prospects of the nuclear waste transmutation; Mise au point d'une methodologie innovante pour la mesure du potentiel d'incineration d'actinides mineurs sous des sources tres intenses de neutrons, dans la perspective de transmutation des dechets nucleaires

    Energy Technology Data Exchange (ETDEWEB)

    Fadil, M

    2003-03-01

    This work deals generally with the problem of nuclear waste management and especially with the transmutation of it to reduce considerably its radiotoxicity potential. The principal objective of this thesis is to show the feasibility to measure on-line the incineration potential of minor actinides irradiated under very high neutron flux. To realize this goal, we have developed fission micro-chambers able to operate, for the first time in the world, in saturation regime under a severe neutron flux. These new chambers use {sup 235}U as an active deposit. They were irradiated in the high flux reactor at Laue-Langevin Institute in Grenoble. The measurement of the saturation current delivered by these chambers during their irradiation for 26 days allowed to evaluate the burn-up of {sup 235}U. We have determined the neutron flux intensity of 1,6 10{sup 15} n.cm{sup -2}.s{sup -1} in the bottom of the irradiation tube called 'V4'. The relative uncertainty of this value is less than 4 %. This is for the first time that such high neutron flux is measured with a fission chamber. To confirm this result, we have also performed independent measurements using gamma spectroscopy of irradiated Nb and Co samples. Both results are in agreement within error bars. Simple Deposit Fission Chambers (SDFC) as above were the reference of the new generation of fission chambers that we have developed in the framework of this thesis: Double Deposit Fission Chambers (DDFC). The reference active deposit was {sup 235}U. The other deposit was the actinide that we wanted to study (e.g. {sup 237}Np and {sup 241}Am). At the end of the thesis, we present some suggestions to ameliorate the operation of the DDFC to be exploited in other transmutation applications in the future. (author)

  9. Conceptual study of fusion-driven system for nuclear waste transmutation

    Energy Technology Data Exchange (ETDEWEB)

    Hong, B.G., E-mail: bghong@jbnu.ac.kr

    2014-10-15

    A conceptual study of a fusion-driven system for nuclear waste transmutation using a low aspect ratio (LAR) tokamak as a neutron source is performed. A configuration of the LAR tokamak neutron source optimised with respect to both transmutation rate and the tritium breeding ratio for aspect ratio A in the range of 1.5–2.0 is found. The transmutation characteristics of both transuranic actinides and minor actinides are investigated and compared. When the transuranic actinides are loaded in the blanket, the neutron multiplication factor decreases from its initial value, k{sub eff} = 0.95, but with the minor actinides loaded in the blanket, the neutron multiplication factor shows a peak value during burn-up. The peak value can be controlled by adjusting the blanket dimensions. To transmute the nuclear waste effectively, an equilibrium fuel cycle is developed for both transuranic actinide and minor actinide transmutation.

  10. Investigation of the Feasibility of a Small Scale Transmutation Device

    OpenAIRE

    Sit, Roger Carson

    2009-01-01

    This dissertation presents the design and feasibility of a small-scale, fusion-based transmutation device incorporating a commercially available neutron generator. It also presents the design features necessary to optimize the device and render it practical for the transmutation of selected long-lived fission products and actinides.Four conceptual designs of a transmutation device were used to study the transformation of seven radionuclides: long-lived fission products (Tc-99 and I-129), sho...

  11. Vortex transmutation.

    Science.gov (United States)

    Ferrando, Albert; Zacarés, Mario; García-March, Miguel-Angel; Monsoriu, Juan A; de Córdoba, Pedro Fernández

    2005-09-16

    Using group theory arguments and numerical simulations, we demonstrate the possibility of changing the vorticity or topological charge of an individual vortex by means of the action of a system possessing a discrete rotational symmetry of finite order. We establish on theoretical grounds a "transmutation pass" determining the conditions for this phenomenon to occur and numerically analyze it in the context of two-dimensional optical lattices. An analogous approach is applicable to the problems of Bose-Einstein condensates in periodic potentials.

  12. Investigation of the feasibility of a small scale transmutation device

    Science.gov (United States)

    Sit, Roger Carson

    This dissertation presents the design and feasibility of a small-scale, fusion-based transmutation device incorporating a commercially available neutron generator. It also presents the design features necessary to optimize the device and render it practical for the transmutation of selected long-lived fission products and actinides. Four conceptual designs of a transmutation device were used to study the transformation of seven radionuclides: long-lived fission products (Tc-99 and I-129), short-lived fission products (Cs-137 and Sr-90), and selective actinides (Am-241, Pu-238, and Pu-239). These radionuclides were chosen because they are major components of spent nuclear fuel and also because they exist as legacy sources that are being stored pending a decision regarding their ultimate disposition. The four designs include the use of two different devices; a Deuterium-Deuterium (D-D) neutron generator (for one design) and a Deuterium-Tritium (D-T) neutron generator (for three designs) in configurations which provide different neutron energy spectra for targeting the radionuclide for transmutation. Key parameters analyzed include total fluence and flux requirements; transmutation effectiveness measured as irradiation effective half-life; and activation products generated along with their characteristics: activity, dose rate, decay, and ingestion and inhalation radiotoxicity. From this investigation, conclusions were drawn about the feasibility of the device, the design and technology enhancements that would be required to make transmutation practical, the most beneficial design for each radionuclide, the consequence of the transmutation, and radiation protection issues that are important for the conceptual design of the transmutation device. Key conclusions from this investigation include: (1) the transmutation of long-lived fission products and select actinides can be practical using a small-scale, fusion driven transmutation device; (2) the transmutation of long

  13. On fusion driven systems (FDS) for transmutation

    Energy Technology Data Exchange (ETDEWEB)

    Aagren, O (Uppsala Univ., Aangstroem laboratory, div. of electricity, Uppsala (Sweden)); Moiseenko, V.E. (Inst. of Plasma Physics, National Science Center, Kharkov Inst. of Physics and Technology, Kharkov (Ukraine)); Noack, K. (Forschungszentrum Dresden-Rossendorf (Germany))

    2008-10-15

    This report gives a brief description of ongoing activities on fusion driven systems (FDS) for transmutation of the long-lived radioactive isotopes in the spent nuclear waste from fission reactors. Driven subcritical systems appears to be the only option for efficient minor actinide burning. Driven systems offer a possibility to increase reactor safety margins. A comparatively simple fusion device could be sufficient for a fusion-fission machine, and transmutation may become the first industrial application of fusion. Some alternative schemes to create strong fusion neutron fluxes are presented

  14. Partitioning and Transmutation. Annual Report 2004

    Energy Technology Data Exchange (ETDEWEB)

    Andersson, Sofie; Drouet, Francois; Ekberg, Christian; Liljenzin, Jan-Olov; Magnusson, Daniel; Nilsson, Mikael; Retegan, Teodora; Skarnemark, Gunnar [Chalmers Univ. of Technology, Goeteborg (Sweden). Dept. of Materials and Surface Chemistry

    2005-01-01

    The long-lived elements in the spent nuclear fuels are mostly actinides, some fission products ({sup 129}I, {sup 99}Tc, {sup 135}Cs, {sup 93}Zr and {sup 126}Sn and activation products ({sup 14}C and {sup 36}Cl). To be able to destroy the long-lived elements in a transmutation process they must be separated from the rest of the spent nuclear fuel. The most difficult separations to make are those between trivalent actinides and lanthanides, due to their relatively similar chemical properties, and those between different actinides themselves. This separation is necessary to obtain the desired efficiency in the transmutation process in order not to create any unnecessary waste thus rendering the process useless. Solvent extraction is an efficient and well-known method that makes it possible to have separation factors that fulfil the highly set demands on purity of the separated phases and on small losses. Chalmers University of Technology is involved in research regarding the separation of actinides and lanthanides and between the actinides themselves as a partner in the European Union sixth framework program project EUROPART. This is a continuation of the projects we participated in within the fourth and fifth framework programmes NEWPART and PARTNEW respectively. The aims of the projects have now shifted from basic understanding to more applied research with focus on process development.

  15. Tokamak Transmutation of (nuclear) Waste (TTW): Parametric studies

    Science.gov (United States)

    Cheng, E. T.; Krakowski, R. A.; Peng, Y. K. M.

    Radioactive waste generated as part of the commercial-power and defense nuclear programs can be either stored or transmuted. The latter treatment requires a capital-intensive neutron source and is reserved for particularly hazardous and long-lived actinide and fission-product waste. A comparative description of fusion-based transmutation is made on the basis of rudimentary estimates of ergonic performance and transmutation capacities versus inventories for both ultra-low aspect-ratio (spherical torus, ST) and conversional (aspect-ratio) tokamak fusion-power-core drivers. The parametric systems studies reported herein provides a preamble to more-detailed, cost-based systems analyses.

  16. Partitioning and Transmutation. Annual Report 2006

    Energy Technology Data Exchange (ETDEWEB)

    Dubois, Isabelle; Englund, Sofie; Fermvik, Anna; Liljenzin, Jan-Olov; Neumayer, Denis; Retegan, Teodora; Skarnemark, Gunnar [Chalmers Univ. of Technology, Goeteborg (Sweden). Dept. of Chemical and Biological Engineering

    2007-01-15

    The long-lived elements in the spent nuclear fuels are mostly actinides, some fission products ({sup 79}Se, {sup 87}Rb, {sup 99}Tc, {sup 107}Pd, {sup 126}Sn, {sup 129}I, {sup 135}Cs) and activation products ({sup 14}C, {sup 36}Cl, {sup 59}Ni, {sup 93} Zr, {sup 94} To be able to destroy the long-lived elements in a transmutation process they must be separated from the rest of the spent nuclear fuel. The most difficult separations to make are those between trivalent actinides and lanthanides, due to their relatively similar chemical properties, and those between different actinides themselves. These separations are necessary to obtain the desired efficiency of the transmutation process and in order not to create any unnecessary waste thus rendering the process useless. Solvent extraction is an efficient and well-known method that makes it possible to have separation factors that fulfil the highly set demands on purity of the separated phases and on small losses. Chalmers University of Technology is involved in research regarding the separation of actinides and lanthanides and between the actinides themselves as a partner in the EUROPART project within the European Union sixth framework program. This is a continuation of the projects we participated in within the fourth and fifth framework programmes, NEWPART and PARTNEW, respectively. The aims of the projects have now shifted from basic understanding to more applied research with focus on process development. However, since the basic understanding is still needed we have our main focus on the chemical processes and understanding of how they work. Work is progressing in relation to a proposal for the 7th framework programme. This proposal will be aiming at a pilot plant for separation for transmutation purposes.

  17. FCRD Transmutation Fuels Handbook 2015

    Energy Technology Data Exchange (ETDEWEB)

    Janney, Dawn Elizabeth [Idaho National Lab. (INL), Idaho Falls, ID (United States); Papesch, Cynthia Ann [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2015-09-01

    Transmutation of minor actinides such as Np, Am, and Cm in spent nuclear fuel is of international interest because of its potential for reducing the long-term health and safety hazards caused by the radioactivity of the spent fuel. One important approach to transmutation (currently being pursued by the DOE Fuel Cycle Research & Development Advanced Fuels Campaign) involves incorporating the minor actinides into U-Pu-Zr alloys, which can be used as fuel in fast reactors. It is, therefore, important to understand the properties of U-Pu-Zr alloys, both with and without minor actinide additions. In addition to requiring extensive safety precautions, alloys containing U and Pu are difficult to study for numerous reasons, including their complex phase transformations, characteristically sluggish phase-transformation kinetics, tendency to produce experimental results that vary depending on the histories of individual samples, and sensitivity to contaminants such as oxygen in concentrations below a hundred parts per million. Many of the experimental measurements were made before 1980, and the level of documentation for experimental methods and results varies widely. It is, therefore, not surprising that little is known with certainty about U-Pu-Zr alloys, and that general acceptance of results sometimes indicates that there is only a single measurement for a particular property. This handbook summarizes currently available information about U, Pu, Zr, and alloys of two or three of these elements. It contains information about phase diagrams and related information (including phases and phase transformations); heat capacity, entropy, and enthalpy; thermal expansion; and thermal conductivity and diffusivity. In addition to presenting information about materials properties, it attempts to provide information about how well the property is known and how much variation exists between measurements. Although the handbook includes some references to publications about modeling

  18. Transmutation Performance Analysis for Inert Matrix Fuels in Light Water Reactors and Computational Neutronics Methods Capabilities at INL

    Energy Technology Data Exchange (ETDEWEB)

    Michael A. Pope; Samuel E. Bays; S. Piet; R. Ferrer; Mehdi Asgari; Benoit Forget

    2009-05-01

    The urgency for addressing repository impacts has grown in the past few years as a result of Spent Nuclear Fuel (SNF) accumulation from commercial nuclear power plants. One path that has been explored by many is to eliminate the transuranic (TRU) inventory from the SNF, thus reducing the need for additional long term repository storage sites. One strategy for achieving this is to burn the separated TRU elements in the currently operating U.S. Light Water Reactor (LWR) fleet. Many studies have explored the viability of this strategy by loading a percentage of LWR cores with TRU in the form of either Mixed Oxide (MOX) fuels or Inert Matrix Fuels (IMF). A task was undertaken at INL to establish specific technical capabilities to perform neutronics analyses in order to further assess several key issues related to the viability of thermal recycling. The initial computational study reported here is focused on direct thermal recycling of IMF fuels in a heterogeneous Pressurized Water Reactor (PWR) bundle design containing Plutonium, Neptunium, Americium, and Curium (IMF-PuNpAmCm) in a multi-pass strategy using legacy 5 year cooled LWR SNF. In addition to this initial high-priority analysis, three other alternate analyses with different TRU vectors in IMF pins were performed. These analyses provide comparison of direct thermal recycling of PuNpAmCmCf, PuNpAm, PuNp, and Pu. The results of this infinite lattice assembly-wise study using SCALE 5.1 indicate that it may be feasible to recycle TRU in this manner using an otherwise typical PWR assembly without violating peaking factor limits.

  19. Accelerator-driven transmutation of spent fuel elements

    Science.gov (United States)

    Venneri, Francesco; Williamson, Mark A.; Li, Ning

    2002-01-01

    An apparatus and method is described for transmuting higher actinides, plutonium and selected fission products in a liquid-fuel subcritical assembly. Uranium may also be enriched, thereby providing new fuel for use in conventional nuclear power plants. An accelerator provides the additional neutrons required to perform the processes. The size of the accelerator needed to complete fuel cycle closure depends on the neutron efficiency of the supported reactors and on the neutron spectrum of the actinide transmutation apparatus. Treatment of spent fuel from light water reactors (LWRs) using uranium-based fuel will require the largest accelerator power, whereas neutron-efficient high temperature gas reactors (HTGRs) or CANDU reactors will require the smallest accelerator power, especially if thorium is introduced into the newly generated fuel according to the teachings of the present invention. Fast spectrum actinide transmutation apparatus (based on liquid-metal fuel) will take full advantage of the accelerator-produced source neutrons and provide maximum utilization of the actinide-generated fission neutrons. However, near-thermal transmutation apparatus will require lower standing

  20. Wastes Management Through Transmutation in an ADS Reactor

    Directory of Open Access Journals (Sweden)

    Bernard Verboomen

    2008-06-01

    Full Text Available The main challenge in nuclear fuel cycle closure is the reduction of the potential radiotoxicity, or of the time in which that possible hazard really exists. Probably, the transmutation of minor actinides with fast fission processes is the most effective answer. This work, performed in SCK⋅CEN (Belgium and DIMNP Pisa University, is focused on preliminary evaluation of industrial scale ADS (400 MWth, 2.5 mA burning capability. An inert matrix fuel of minor actinides, 50% vol. MgO and 50% vol. (Pu,Np,Am,CmO1.88, core content, with 150 GWd/ton discharge burn up, is used. The calculations were performed using ALEPH-1.1.2, MCNPX-2.5.0, and ORIGEN2.2. codes.

  1. Fusion transmutation of waste: design and analysis of the in-zinerator concept.

    Energy Technology Data Exchange (ETDEWEB)

    Durbin, S. M.; Cipiti, Benjamin B.; Olson, Craig Lee; Guild-Bingham, Avery (Texas A& M University, College Station, TX); Venneri, Francesco (General Atomics, San Diego, CA); Meier, Wayne (LLNL, Livermore, CA); Alajo, A.B. (Texas A& M University, College Station, TX); Johnson, T. R. (Argonne Mational Laboratory, Argonne, IL); El-Guebaly, L. A. (University of Wisconsin, Madison, WI); Youssef, M. E. (University of California, Los Angeles, CA); Young, Michael F.; Drennen, Thomas E. (Hobart & William Smith College, Geneva, NY); Tsvetkov, Pavel Valeryevich (Texas A& M University, College Station, TX); Morrow, Charles W.; Turgeon, Matthew C.; Wilson, Paul (University of Wisconsin, Madison, WI); Phruksarojanakun, Phiphat (University of Wisconsin, Madison, WI); Grady, Ryan (University of Wisconsin, Madison, WI); Keith, Rodney L.; Smith, James Dean; Cook, Jason T.; Sviatoslavsky, Igor N. (University of Wisconsin, Madison, WI); Willit, J. L. (Argonne Mational Laboratory, Argonne, IL); Cleary, Virginia D.; Kamery, William (Hobart & William Smith College, Geneva, NY); Mehlhorn, Thomas Alan; Rochau, Gary Eugene

    2006-11-01

    Due to increasing concerns over the buildup of long-lived transuranic isotopes in spent nuclear fuel waste, attention has been given in recent years to technologies that can burn up these species. The separation and transmutation of transuranics is part of a solution to decreasing the volume and heat load of nuclear waste significantly to increase the repository capacity. A fusion neutron source can be used for transmutation as an alternative to fast reactor systems. Sandia National Laboratories is investigating the use of a Z-Pinch fusion driver for this application. This report summarizes the initial design and engineering issues of this ''In-Zinerator'' concept. Relatively modest fusion requirements on the order of 20 MW can be used to drive a sub-critical, actinide-bearing, fluid blanket. The fluid fuel eliminates the need for expensive fuel fabrication and allows for continuous refueling and removal of fission products. This reactor has the capability of burning up 1,280 kg of actinides per year while at the same time producing 3,000 MWth. The report discusses the baseline design, engineering issues, modeling results, safety issues, and fuel cycle impact.

  2. Optimization of accelerator-driven technology for LWR waste transmutation

    Energy Technology Data Exchange (ETDEWEB)

    Bowman, C.D.

    1996-12-31

    The role of accelerator-driven transmutation technology is examined in the context of the destruction of actinide waste from commercial light water reactors. It is pointed out that the commercial plutonium is much easier to use for entry-level nuclear weapons than weapons plutonium. Since commercial plutonium is easier to use, since there is very much more of it already, and since it is growing rapidly, the permanent disposition of commercial plutonium is an issue of greater importance than weapons plutonium. The minor actinides inventory, which may be influenced by transmutation, is compared in terms of nuclear properties with commercial and weapons plutonium and for possible utility as weapons material. Fast and thermal spectrum systems are compared as means for destruction of plutonium and the minor actinides. it is shown that the equilibrium fast spectrum actinide inventory is about 100 times larger than for thermal spectrum systems, and that there is about 100 times more weapons-usable material in the fast spectrum system inventory compared to the thermal spectrum system. Finally it is shown that the accelerator size for transmutation can be substantially reduced by design which uses the accelerator-produced neutrons only to initiate the unsustained fission chains characteristic of the subcritical system. The analysis argues for devoting primary attention to the development of thermal spectrum transmutation technology. A thermal spectrum transmuter operating at a fission power of 750-MWth fission power, which is sufficient to destroy the actinide waste from one 3,000-MWth light water reactor, may be driven by a proton beam of 1 GeV energy and a current of 7 mA. This accelerator is within the range of realizable cyclotron technology and is also near the size contemplated for the next generation spallation neutron source under consideration by the US, Europe, and Japan.

  3. Transmutation of radioactive nuclear waste – present status and requirement for the problem-oriented nuclear data base

    Indian Academy of Sciences (India)

    Yu A Korovin; V V Artisyuk; A V Ignatyuk; G B Pilnov; A Yu Stankovsky; Yu E Titarenko; S G Yavshits

    2007-02-01

    Transmutation of long-lived actinides and fission products becomes an important issue of the overall nuclear fuel cycle assessment, both for existing and future reactor systems. Reliable nuclear data are required for analysis of associated neutronics. The present paper gives a review of the status of nuclear data analysis focusing on the waste transmutation problem.

  4. Advanced Gas-Cooled Accelerator-Driven Transmutation Experiment. AGATE; Advanced Gas-Cooled Accelerator-Driven Transmutation Experiment. AGATE

    Energy Technology Data Exchange (ETDEWEB)

    Kettler, John; Biss, Klaus [RWTH Aachen (DE). Inst. fuer Nuklearen Brennstoffkreislauf (INBK); Bongardt, Klaus [RWTH Aachen (DE). Inst. fuer Kernphysik (IKP)] (and others)

    2011-07-01

    In Germany the question of final radioactive waste disposal is not yet decided. For intermediate-level radioactive waste the final repository Konrad is licensed, for the high-level radioactive waste not certified repository exists. Transmutation by neutron reaction can reduce the long-term heat output and the amount of long-living radionuclides (minor actinides MA). Several accelerator-driven transmutation concepts have been discussed in the past. The authors describe preliminary results of a feasibility study of the concept AGATE (advanced gas-cooled accelerator-driven transmutation experiment). An accelerated 600 MeV proton beam on the spallation target that is the neutron source in the subcritical reactor. In the starting phase the concept assumes MOX fuel with 20% Pu. In a later phase an optimized fuel for the MA transmutation has to be elaborated.

  5. Partitioning and transmutation. Annual report 2007

    Energy Technology Data Exchange (ETDEWEB)

    Aneheim, Emma; Ekberg, Christian; Englund, Sofie; Fermvik, Anna; Foreman, Mark St. J.; Liljenzin, Jan-Olov; Retegan, Teodora; Skarnemark, Gunnar; Wald, Karin (Nuclear Chemistry, Dept. of Chemical and Biological Engineering, Chalmers Univ. of Technology, Goeteborg (SE))

    2007-01-15

    The long-lived elements in the spent nuclear fuels are mostly actinides, some fission products (79Se, 87Rb, 99Tc, 107Pd, 126Sn, 129I, 135Cs) and activation products (14C, 36Cl, 59Ni, 93Zr, 94Nb). To be able to destroy the long-lived elements in a transmutation process they must be separated from the rest of the spent nuclear fuel. The most difficult separations to make are those between trivalent actinides and lanthanides, due to their relatively similar chemical properties, and those between different actinides themselves. These separations are necessary to obtain the desired efficiency of the transmutation process and in order not to create any unnecessary waste thus rendering the process useless. Solvent extraction is an efficient and well-known method that makes it possible to have separation factors that fulfil the highly set demands on purity of the separated phases and on small losses. Chalmers University of Technology is involved in research regarding the separation of actinides and lanthanides and between the actinides themselves as a partner in several European frame work programmes from NEWPART in the 4th framework via PARTNEW and EUROPART to ACSEPT now in the 7th programme. The aims of the projects have now shifted from basic understanding to more applied research with focus on process development. However, since a further investigation on basic understanding of the chemical behaviour is required, we have our main focus on the chemical processes and understanding of how they work. Due to new recruitments we will now also work on ligand design and development. This will decrease the response time between new ligands and their evaluation.

  6. Partitioning and transmutation. Annual report 2007

    Energy Technology Data Exchange (ETDEWEB)

    Aneheim, Emma; Ekberg, Christian; Englund, Sofie; Fermvik, Anna; Foreman, Mark St. J.; Liljenzin, Jan-Olov; Retegan, Teodora; Skarnemark, Gunnar; Wald, Karin (Nuclear Chemistry, Dept. of Chemical and Biological Engineering, Chalmers Univ. of Technology, Goeteborg (SE))

    2007-01-15

    The long-lived elements in the spent nuclear fuels are mostly actinides, some fission products (79Se, 87Rb, 99Tc, 107Pd, 126Sn, 129I, 135Cs) and activation products (14C, 36Cl, 59Ni, 93Zr, 94Nb). To be able to destroy the long-lived elements in a transmutation process they must be separated from the rest of the spent nuclear fuel. The most difficult separations to make are those between trivalent actinides and lanthanides, due to their relatively similar chemical properties, and those between different actinides themselves. These separations are necessary to obtain the desired efficiency of the transmutation process and in order not to create any unnecessary waste thus rendering the process useless. Solvent extraction is an efficient and well-known method that makes it possible to have separation factors that fulfil the highly set demands on purity of the separated phases and on small losses. Chalmers University of Technology is involved in research regarding the separation of actinides and lanthanides and between the actinides themselves as a partner in several European frame work programmes from NEWPART in the 4th framework via PARTNEW and EUROPART to ACSEPT now in the 7th programme. The aims of the projects have now shifted from basic understanding to more applied research with focus on process development. However, since a further investigation on basic understanding of the chemical behaviour is required, we have our main focus on the chemical processes and understanding of how they work. Due to new recruitments we will now also work on ligand design and development. This will decrease the response time between new ligands and their evaluation.

  7. Partitioning and Transmutation. Annual Report 2005

    Energy Technology Data Exchange (ETDEWEB)

    Andersson, Sofie; Ekberg, Christian; Fermvik, Anna; Hervieux, Nadege; Liljenzin, Jan-Olov; Magnusson, Daniel; Nilsson, Mikael; Retegan, Teodora; Skarnemark, Gunnar [Chalmers Univ. of Technology, Goeteborg (Sweden). Dept. of Chemical and Biological Engineering

    2006-01-15

    The long-lived elements in the spent nuclear fuels are mostly actinides, some fission products ({sup 79}Se, {sup 87}Rb, {sup 99}Tc, {sup 107}Pd, {sup 126}Sn, {sup 129}I, {sup 135}Cs) and activation products ({sup 14}C, {sup 36}Cl, {sup 59}Ni, {sup 93}Zr, {sup 94}N To be able to destroy the long-lived elements in a transmutation process they must be separated from the rest of the spent nuclear fuel. The most difficult separations to make are those between trivalent actinides and lanthanides, due to their relatively similar chemical properties, and those between different actinides themselves. These separations are necessary to obtain the desired efficiency of the transmutation process and in order not to create any unnecessary waste thus rendering the process useless. Solvent extraction is an efficient and well-known method that makes it possible to have separation factors that fulfil the highly set demands on purity of the separated phases and on small losses. Chalmers Univ. of Technology is involved in research regarding the separation of actinides and lanthanides and between the actinides themselves as a partner in the EUROPART project within the European Union sixth framework program. This is a continuation of the projects we participated in within the fourth and fifth framework programmes, NEWPART and PARTNEW respectively. The aims of the projects have now shifted from basic understanding to more applied research with focus on process development. However, since the basic understanding is still needed we have our main focus on the chemical processes and understanding of how they work.

  8. Transuranics Transmutation Using Neutrons Spectrum from Spallation Reactions

    Directory of Open Access Journals (Sweden)

    Maurício Gilberti

    2015-01-01

    Full Text Available The aim is to analyse the neutron spectrum influence in a hybrid system ADS-fission inducing transuranics (TRUs transmutation. A simple model consisting of an Accelerator-Driven Subcritical (ADS system containing spallation target, moderator or coolant, and spheres of actinides, “fuel,” at different locations in the system was modelled. The simulation was performed using the MCNPX 2.6.0 particles transport code evaluating capture (n,γ and fission (n,f reactions, as well as the burnup of actinides. The goal is to examine the behaviour and influences of the hard neutron spectrum from spallation reactions in the transmutation, without the contribution or interference of multiplier subcritical medium, and compare the results with those obtained from the neutron fission spectrum. The results show that the transmutation efficiency is independent of the spallation target material used, and the neutrons spectrum from spallation does not contribute to increased rates of actinides transmutation even in the vicinity of the target.

  9. Transmutation of radioactive nuclear waste

    Energy Technology Data Exchange (ETDEWEB)

    Toor, A; Buck, R

    2000-03-15

    years. One approach to the RNW storage problem has been to transmute the radioactive elements into other radioactive isotopes with much shorter half-lives. Transmutation of both RNW components using neutrons has been discussed and studied over the past four decades. Most transmutation studies have examined the feasibility of using neutron-induced reactions where the neutrons would be provided by accelerator-based spallation neutron sources, tokamak fusion reactors, sub-critical fission reactors and other novel concepts. Studies have shown that all proposed transmutation processes to treat RNW using neutron reactions are deficient or marginal at best from the point of view of energy consumption and/or cost. We suggest an alternative approach that has not been considered to date: the transmutation of RNW elements using high-energy photons or gamma rays. The photo-disintegration of RNW may provide an effective way to treat reprocessed waste; waste that has been chemically separated or the residual waste left over after neutron processing. Photo-disintegration is attractive in that any isotope can be transmuted. This approach is now potentially practical because of the development of micropole undulators (MPUs) that allow us to use small storage rings to economically generate photons with gamma-ray energies and to tune these ''gamma rays'' to the peak of the cross-section resonance for various RNW elements. Because the cross sections for all RNW nuclei have a broad peak with the maximum in the 12-18 MeV range, a single MPU could be used to treat both actinide and fission fragment components of RNW. The goal of this study is to make estimates of the reaction rates and energy efficiency of the transmutation of typical RNW elements using gamma rays to establish whether or not gamma-ray transmutation should be examined as a viable alternative solution to RNW warranting further study.

  10. Industrial research for transmutation scenarios

    Science.gov (United States)

    Camarcat, Noel; Garzenne, Claude; Le Mer, Joël; Leroyer, Hadrien; Desroches, Estelle; Delbecq, Jean-Michel

    2011-04-01

    This article presents the results of research scenarios for americium transmutation in a 22nd century French nuclear fleet, using sodium fast breeder reactors. We benchmark the americium transmutation benefits and drawbacks with a reference case consisting of a hypothetical 60 GWe fleet of pure plutonium breeders. The fluxes in the various parts of the cycle (reactors, fabrication plants, reprocessing plants and underground disposals) are calculated using EDF's suite of codes, comparable in capabilities to those of other research facilities. We study underground thermal heat load reduction due to americium partitioning and repository area minimization. We endeavor to estimate the increased technical complexity of surface facilities to handle the americium fluxes in special fuel fabrication plants, americium fast burners, special reprocessing shops, handling equipments and transport casks between those facilities.

  11. Partitioning and transmutation (P and T) 1997. Status report

    Energy Technology Data Exchange (ETDEWEB)

    Enarsson, Aasa; Landgren, A.; Liljenzin, J.O.; Skaalberg, M.; Spjuth, L. [Chalmers Univ. of Technology, Goeteborg (Sweden). Dept. of Nuclear Chemistry; Gudowski, W.; Wallenius, J. [Royal Inst. of Tech., Stockholm (Sweden). Dept. of Nuclear and Reactor Physics

    1998-05-01

    ultimately applied, as a rule, it can be stated that 3-4 reactors are necessary with a high-energy neutron spectrum to transmute waste from the Swedish light water reactor park. Thus, the Swedish research programme on transmutation systems, should perhaps focus on studies of fast reactor systems for transmutation, especially heavy metal-cooled systems with or without connected neutron-producing accelerators. Studies of fuel types which are suitable for transmutation, such as oxides and mono nitrides are of particular interest. At the same time, calculations of the efficiency of the fission product transmutation in accelerator-driven systems should be carried out. Measurements of less well-known cross-sections for reactions which are of importance for the transmutation of certain actinides are also required as a basis for such work 80 refs, 6 tabs, 7 figs

  12. Subsurface Biogeochemistry of Actinides

    Energy Technology Data Exchange (ETDEWEB)

    Kersting, Annie B. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States). Univ. Relations and Science Education; Zavarin, Mavrik [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States). Glenn T. Seaborg Inst.

    2016-06-29

    A major scientific challenge in environmental sciences is to identify the dominant processes controlling actinide transport in the environment. It is estimated that currently, over 2200 metric tons of plutonium (Pu) have been deposited in the subsurface worldwide, a number that increases yearly with additional spent nuclear fuel (Ewing et al., 2010). Plutonium has been shown to migrate on the scale of kilometers, giving way to a critical concern that the fundamental biogeochemical processes that control its behavior in the subsurface are not well understood (Kersting et al., 1999; Novikov et al., 2006; Santschi et al., 2002). Neptunium (Np) is less prevalent in the environment; however, it is predicted to be a significant long-term dose contributor in high-level nuclear waste. Our focus on Np chemistry in this Science Plan is intended to help formulate a better understanding of Pu redox transformations in the environment and clarify the differences between the two long-lived actinides. The research approach of our Science Plan combines (1) Fundamental Mechanistic Studies that identify and quantify biogeochemical processes that control actinide behavior in solution and on solids, (2) Field Integration Studies that investigate the transport characteristics of Pu and test our conceptual understanding of actinide transport, and (3) Actinide Research Capabilities that allow us to achieve the objectives of this Scientific Focus Area (SFA and provide new opportunities for advancing actinide environmental chemistry. These three Research Thrusts form the basis of our SFA Science Program (Figure 1).

  13. Study of particle transport in a high power spallation target for an accelerator driven transmutation system

    OpenAIRE

    Shetty, Nikhil Vittal

    2013-01-01

    Transmutation of highly radioactive nuclear waste can be performed using an accelerator driven system (ADS), where high energy protons impinge on a spallation target to produce neutrons. These neutrons are multiplied in a subcritical core, while simultaneously fissioning the minor actinides into short lived or stable nuclides. AGATE is a project envisaged to demonstrate the feasibility of transmutation in a gas (helium) cooled ADS using solid spallation target. Development of the spallation t...

  14. Actinides-1981

    Energy Technology Data Exchange (ETDEWEB)

    1981-09-01

    Abstracts of 134 papers which were presented at the Actinides-1981 conference are presented. Approximately half of these papers deal with electronic structure of the actinides. Others deal with solid state chemistry, nuclear physic, thermodynamic properties, solution chemistry, and applied chemistry.

  15. Transmutation Technology Development

    Energy Technology Data Exchange (ETDEWEB)

    Song, T. Y.; Park, W. S.; Kim, Y. H. (and others)

    2007-06-15

    The spent fuel coming from the PWR is one of the most difficult problems to be solved for the continuous use of nuclear power. It takes a few million years to be safe under the ground. Therefore, it is not easy to take care of the spent fuel for such a long time. Transmutation technology is the key technology which can solve the spent fuel problem basically. Transmutation is to transmute long-lived radioactive nuclides in the spent fuel into short-lived or stable nuclide through nuclear reactions. The long-lived radioactive nuclides can be TRU and fission products such as Tc-99 and I-129. Although the transmutation technology does not make the underground disposal totally unnecessary, the period to take care of the spent fuel can be reduced to the order of a few hundred years. In addition to the environmental benefit, transmutation can be considered to recycle the energy in the spent fuel since the transmutation is performed through nuclear fission reaction of the TRU in the spent fuel. Therefore, transmutation technology is worth being developed in economical aspect. The results of this work can be a basis for the next stage research. The objective of the third stage research was to complete the core conceptual design and verification of the key technologies. The final results will contribute to the establishment of Korean back end fuel cycle policy by providing technical guidelines.

  16. Transmutation of high-level radioactive waste - Perspectives

    CERN Document Server

    Junghans, Arnd; Grosse, Eckart; Hannaske, Roland; Kögler, Toni; Massarczyk, Ralf; Schwengner, Ronald; Wagner, Andreas

    2014-01-01

    In a fast neutron spectrum essentially all long-lived actinides (e.g. Plutonium) undergo fission and thus can be transmuted into generally short lived fission products. Innovative nuclear reactor concepts e.g. accelerator driven systems (ADS) are currently in development that foresee a closed fuel cycle. The majority of the fissile nuclides (uranium, plutonium) shall be used for power generation and only fission products will be put into final disposal that needs to last for a historical time scale of only 1000 years. For the transmutation of high-level radioactive waste a lot of research and development is still required. One aspect is the precise knowledge of nuclear data for reactions with fast neutrons. Nuclear reactions relevant for transmutation are being investigated in the framework of the european project ERINDA. First results from the new neutron time-of-flight facility nELBE at Helmholtz-Zentrum Dresden-Rossendorf will be presented.

  17. The nuclear fuel cycle for transmutation: a critical review

    Energy Technology Data Exchange (ETDEWEB)

    Kuster, H.; Kienzler, B.; Kolarik, Z.; Wiese, H.W. [Forschungszentrum Karlsruhe, FZK (Germany); Segev, M. [Ben Gurion University, Beer Sheba (Israel); Salvadores, M.; Slesarev, I.; Zaetta, A. [CEA Cadarache, 13 - Saint-Paul-lez-Durance (France)

    1995-12-31

    This review presents a critical common FZK and CEA discussion of the transmutation possibilities of actinide nuclei and of fission products as Tc and I in reactors (PWRs and FBRs) and in accelerator-driven subcritical configurations. The activities in the Research Center Karlsruhe in the chemical area are briefly discussed. Activities in the chemical area at CEA are presented elsewhere at this conference. The alternate waste disposal with transmutation is compared to the direct disposal option, as seen from the FZK point of view. Work in France on this point is still underway according to a law, voted in the French Parliament in 1991. The aim of this study is to evaluate, how the short-term and long-term risks of nuclear waste, including both direct disposal and transmutation scenarios, realistically could be minimized. (authors) 30 refs.

  18. Specific contributions of the Dutch progamme ``RAS`` towards accelerator-based transmutation

    Energy Technology Data Exchange (ETDEWEB)

    Abrahams, K.; Franken, W.M.P.; Bultman, J.H.; Heil, J.A.; Koning, A.J.

    1994-09-01

    Accelerator-based transmutation is being studied by ECN within its general nuclear waste transmutation programme RAS. In this paper the following contributions are presented: (1) Evaluation of cross sections at intermediate energies, within an international frame given by NEA, (2) Cell calculations on the equilibration of transuranium actinides in thermal molten-salt transmuters, (3) Irradiation facilities at the European research reactor HFR in Petten, which have been constructed with the purpose to demonstrate and investigate the transmutation of waste in a high neutron flux, (4) Studies of accelerator-based neutron generating systems to transmute neptunium and technetium, (5) Comparison of several systems on the basis of criteria for successful nuclear waste-management. (orig.).

  19. Design of unique pins for irradiation of higher actinides in a fast reactor

    Energy Technology Data Exchange (ETDEWEB)

    Basmajian, J.A.; Birney, K.R.; Weber, E.T.; Adair, H.L.; Quinby, T.C.; Raman, S.; Butler, J.K.; Bateman, B.C.; Swanson, K.M.

    1982-03-01

    The actinides produced by transmutation reactions in nuclear reactor fuels are a significant factor in nuclear fuel burnup, transportation and reprocessing. Irradiation testing is a primary source of data of this type. A segmented pin design was developed which provides for incorporation of multiple specimens of actinide oxides for irradiation in the UK's Prototype Fast Reactor (PFR) at Dounreay Scotland. Results from irradiation of these pins will extend the basic neutronic and material irradiation behavior data for key actinide isotopes.

  20. Partitioning and transmutation (P and D) 1995. A review of the current state of the art

    Energy Technology Data Exchange (ETDEWEB)

    Skaalberg, M.; Landgren, A.; Spjuth, L.; Liljenzin, J.O. [Chalmers Univ. of Technology, Goeteborg (Sweden). Dept. of Nuclear Chemistry; Gudowski, W. [Royal Inst. of Tech., Stockholm (Sweden). Dept. of Neutron and Reactor Physics

    1995-12-01

    The recent development in the field of partitioning and transmutation (P/T) is reviewed and evaluated. Current national and international R and D efforts are summarized. Nuclear transmutation with energy production is feasible in nuclear reactors where fast and thermal breeders are the most efficient for transmutation purposes. The operation of subcritical nuclear reactors by high current proton accelerators that generate neutrons in a spallation target is also an interesting option for transmutation and energy production, that has to be more carefully evaluated. These accelerator-driven systems are probably the only solution for the transmutation of long-lived fission products with small neutron capture cross sections and actinide isotopes with small fission cross sections. The requirements on the separation chemistry in the partitioning process depends on the transmutation strategy chosen. Recent developments in aqueous based separation chemistry opens some interesting possibilities to meet some of the requirements, such as separation of different actinides and some fission products and reduction of secondary waste streams. In the advanced accelerator-driven transmutation systems proposed, liquid fuels such as molten salts are considered. The partitioning processes that can be used for these types of fuel will, however, require a long term research program. The possibility to use centrifuge separation is an interesting partitioning option that recently has been proposed. 51 refs, 7 figs, 3 tabs.

  1. Promises and Challenges of Thorium Implementation for Transuranic Transmutation - 13550

    Energy Technology Data Exchange (ETDEWEB)

    Franceschini, F.; Lahoda, E.; Wenner, M. [Westinghouse Electric Company LLC, Cranberry Township, PA (United States); Lindley, B. [University of Cambridge (United Kingdom); Fiorina, C. [Polytechnic of Milan (Italy); Phillips, C. [Energy Solutions, Richland, WA (United States)

    2013-07-01

    This paper focuses on the challenges of implementing a thorium fuel cycle for recycle and transmutation of long-lived actinide components from used nuclear fuel. A multi-stage reactor system is proposed; the first stage consists of current UO{sub 2} once-through LWRs supplying transuranic isotopes that are continuously recycled and burned in second stage reactors in either a uranium (U) or thorium (Th) carrier. The second stage reactors considered for the analysis are Reduced Moderation Pressurized Water Reactors (RMPWRs), reconfigured from current PWR core designs, and Fast Reactors (FRs) with a burner core design. While both RMPWRs and FRs can in principle be employed, each reactor and associated technology has pros and cons. FRs have unmatched flexibility and transmutation efficiency. RMPWRs have higher fuel manufacturing and reprocessing requirements, but may represent a cheaper solution and the opportunity for a shorter time to licensing and deployment. All options require substantial developments in manufacturing, due to the high radiation field, and reprocessing, due to the very high actinide recovery ratio to elicit the claimed radiotoxicity reduction. Th reduces the number of transmutation reactors, and is required to enable a viable RMPWR design, but presents additional challenges on manufacturing and reprocessing. The tradeoff between the various options does not make the choice obvious. Moreover, without an overarching supporting policy in place, the costly and challenging technologies required inherently discourage industrialization of any transmutation scheme, regardless of the adoption of U or Th. (authors)

  2. Review of actinide nitride properties with focus on safety aspects

    Energy Technology Data Exchange (ETDEWEB)

    Albiol, Thierry [CEA Cadarache, St Paul Lez Durance Cedex (France); Arai, Yasuo [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    2001-12-01

    This report provides a review of the potential advantages of using actinide nitrides as fuels and/or targets for nuclear waste transmutation. Then a summary of available properties of actinide nitrides is given. Results from irradiation experiments are reviewed and safety relevant aspects of nitride fuels are discussed, including design basis accidents (transients) and severe (core disruptive) accidents. Anyway, as rather few safety studies are currently available and as many basic physical data are still missing for some actinide nitrides, complementary studies are proposed. (author)

  3. 次锕系元素在加速器驱动的次临界快堆中嬗变的研究%Study of Transmutation of Minor Actinides in Accelerator-Driven Sub-critical Fast Reactor

    Institute of Scientific and Technical Information of China (English)

    杨永伟; 古玉祥

    2001-01-01

    选取加速器驱动次临界快堆(ADSFR),进行嬗变来自于PWR(U)乏燃料 中次锕系元素 的研究。在堆芯内,燃料为NpAmCm的氧化物,选取液态钠为冷却剂。利用下列程序对所选方 案进行物理计算和分析:LAHET -模拟质子与靶核的相互作用;MCNP4A-模拟次临界包层内 20MeV以下的中子与材料核的相互作用;ORIGEN2-利用MCNP4A的输出提供的一群等效截面对 堆芯进行燃耗计算。计算分析的结果表明:考虑临界安全、功率密度和燃耗等因素,利用所 选方案进行次锕系元素嬗变是可行的。%Accelerator-Driven Sub-critical Fast Reactor (ADSFR)is chosenfor transmu ta tion of minor actinides from the spent fuel of PWR(U). In the core, the fuel type is (PuNpAmCm)Ox. Liquid sodium is chosen as coolant The neutronics calcul ation and analysis of the selected scheme have been done by using the following codes: LAHET, for the simulation of the interaction between the protons and the nuclei of the target; MCNP4A, for the simulation of interaction between neutron s with energy below 20MeV and the nuclei of materials in the sub-critical blank e t; ORIGEN2, for the multi-region burnup calculation of the blanket by using the one-group effective cross-section provided in the output of MCNP4A. The neutro ni cs calculation and analysis show that the proposed scheme is feasible for trans mutation of minor actinides, considering the factors such as the criticality s afety, power density, burnup, etc.

  4. Axial Neutron Flux Evaluation in a Tokamak System: a Possible Transmutation Blanket Position for a Fusion-Fission Transmutation System

    Science.gov (United States)

    Velasquez, Carlos E.; de P. Barros, Graiciany; Pereira, Claubia; Fortini Veloso, Maria A.; Costa, Antonella L.

    2012-08-01

    A sub-critical advanced reactor based on Tokamak technology with a D-T fusion neutron source is an innovative type of nuclear system. Due to the large number of neutrons produced by fusion reactions, such a system could be useful in the transmutation process of transuranic elements (Pu and minor actinides (MAs)). However, to enhance the MA transmutation efficiency, it is necessary to have a large neutron wall loading (high neutron fluence) with a broad energy spectrum in the fast neutron energy region. Therefore, it is necessary to know and define the neutron fluence along the radial axis and its characteristics. In this work, the neutron flux and the interaction frequency along the radial axis are evaluated for various materials used to build the first wall. W alloy, beryllium, and the combination of both were studied, and the regions more suitable to transmutation were determined. The results demonstrated that the best zone in which to place a transmutation blanket is limited by the heat sink and the shield block. Material arrangements of W alloy/W alloy and W alloy/beryllium would be able to meet the requirements of the high fluence and hard spectrum that are needed for transuranic transmutation. The system was simulated using the MCNP code, data from the ITER Final Design Report, 2001, and the Fusion Evaluated Nuclear Data Library/MC-2.1 nuclear data library.

  5. Partitioning and transmutation. Annual report 2008

    Energy Technology Data Exchange (ETDEWEB)

    Aneheim, Emma; Ekberg, Christian; Fermvik, Anna; Foreman, Mark; Naestren, Catharina; Retegan, Teodora; Skarnemark, Gunnar (Nuclear Chemistry, Dept. of Chemical and Biological Engineering, Chalmers Univ. of Technology, Goeteborg (Sweden))

    2009-01-15

    The long-lived elements in the spent nuclear fuels are mostly actinides, some fission products (79Se, 87Rb, 99Tc, 107Pd, 126Sn, 129I, 135Cs) and activation products (14C, 36Cl, 59Ni, 93Zr, 94Nb). To be able to destroy the long-lived elements in a transmutation process they must be separated from the rest of the spent nuclear fuel for different reasons. One being high cross sections for neutron capture of some elements, like the lanthanides. Other reasons may be the unintentional making of other long lived isotopes. The most difficult separations to make are those between trivalent actinides and lanthanides, due to their relatively similar chemical properties, and those between different actinides themselves. Solvent extraction is an efficient and well-known method that makes it possible to have separation factors that fulfil the highly set demands on purity of the separated phases and on small losses. In the case of a fuel with a higher burnup or possible future fuels, pyro processing may be of higher advantage due to the limited risk of criticality during the process. Chalmers University of Technology is involved in research regarding the separation of actinides and lanthanides and between the actinides themselves as a partner in several European frame work programmes from NEWPART in the 4th framework via PARTNEW and EUROPART to ACSEPT in the present 7th programme. The aims of the projects have now shifted from basic understanding to more applied research with focus on process development. One process, the SANEX (Selective ActiNide EXtraction) is now considered to be working on a basic scale and focus has moved on to more process oriented areas. However, since further investigations on basic understanding of the chemical behaviour are required, we have our main focus on the chemical processes and understanding of how they work. Our work is now manly focussed on the so called GANEX (Group ActiNide EXtraction) process. Due to new recruitments we will now also work

  6. Partitioning and transmutation. Annual report 2009

    Energy Technology Data Exchange (ETDEWEB)

    Aneheim, Emma; Ekberg, Christian; Fermvik, Anna; Foreman, Mark; Loefstroem-Engdahl, Elin; Retegan, Teodora; Skarnemark, Gunnar; Spendlikova, Irena (Nuclear Chemistry, Department of Chemical and Biological Engineering, Chalmers Univ. of Technology, Goeteborg (Sweden))

    2010-01-15

    The long-lived elements in the spent nuclear fuels are mostly actinides, some fission products (79Se, 87Rb, 99Tc, 107Pd, 126Sn, 129I and 135Cs) and activation products (14C, 36Cl, 59Ni, 93Zr, 94Nb). To be able to destroy the long-lived elements in a transmutation process they must be separated from the rest of the spent nuclear fuel for different reasons. One being high neutron capture cross sections for some elements, like the lanthanides. Other reasons may be the unintentional production of other long lived isotopes. The most difficult separations to make are those between different actinides but also between trivalent actinides and lanthanides, due to their relatively similar chemical properties. Solvent extraction is an efficient and well-known method that makes it possible to have separation factors that fulfil the highly set demands on purity of the separated phases and on small losses. In the case of a fuel with a higher burnup or possible future fuels, pyro processing may be of higher advantage due to the limited risk of criticality during the process. Chalmers University of Technology is involved in research regarding the separation of actinides and lanthanides and between the actinides themselves as a partner in several European frame work programmes. These projects range from NEWPART in the 4th framework via PARTNEW and EUROPART to ACSEPT in the present 7th programme. The aims of the projects have now shifted from basic understanding to more applied research with focus on process development. One process, the SANEX (Selective ActiNide EXtraction) is now considered to be working on a basic scale and focus has moved on to more process oriented areas. However, since further investigations on basic understanding of the chemical behaviour are required, we have our main focus on the chemical processes and understanding of how they work. Our work is now manly focussed on the so called GANEX (Group ActiNide EXtraction) process. We have proposed a novel process

  7. Multi-Reactor Transmutation Analysis Utility (MRTAU,alpha1): Verification

    Energy Technology Data Exchange (ETDEWEB)

    Andrea Alfonsi; Samuel E. Bays; Cristian Rabiti; Steven J. Piet

    2011-02-01

    Multi-Reactor Transmutation Utility (MRTAU) is a general depletion/decay algorithm under development at INL to support quick assessment of off-normal fuel cycle scenarios of similar nature to well studied reactor and fuel cycle concepts for which isotopic and cross-section data exists. MRTAU has been used in the past for scoping calculations to determine actinide composition evolution over the course of multiple recycles in Light Water Reactor Mixed Oxide and Sodium cooled Fast Reactor. In these applications, various actinide partitioning scenarios of interest were considered. The code has recently been expanded to include fission product generation, depletion and isotopic evolution over multiple recycles. The capability was added to investigate potential partial separations and/or limited recycling technologies such as Melt-Refining, AIROX, DUPIC or other fuel recycle technology where the recycled fuel stream is not completely decontaminated of fission products prior to being re-irradiated in a subsequent reactor pass. This report documents the code's solution methodology and algorithm as well as its solution accuracy compared to the SCALE6.0 software suite.

  8. Nuclear Methods for Transmutation of Nuclear Waste: Problems, Perspextives, Cooperative Research - Proceedings of the International Workshop

    Science.gov (United States)

    Khankhasayev, Zhanat B.; Kurmanov, Hans; Plendl, Mikhail Kh.

    1996-12-01

    The Table of Contents for the full book PDF is as follows: * Preface * I. Review of Current Status of Nuclear Transmutation Projects * Accelerator-Driven Systems — Survey of the Research Programs in the World * The Los Alamos Accelerator-Driven Transmutation of Nuclear Waste Concept * Nuclear Waste Transmutation Program in the Czech Republic * Tentative Results of the ISTC Supported Study of the ADTT Plutonium Disposition * Recent Neutron Physics Investigations for the Back End of the Nuclear Fuel Cycle * Optimisation of Accelerator Systems for Transmutation of Nuclear Waste * Proton Linac of the Moscow Meson Factory for the ADTT Experiments * II. Computer Modeling of Nuclear Waste Transmutation Methods and Systems * Transmutation of Minor Actinides in Different Nuclear Facilities * Monte Carlo Modeling of Electro-nuclear Processes with Nonlinear Effects * Simulation of Hybrid Systems with a GEANT Based Program * Computer Study of 90Sr and 137Cs Transmutation by Proton Beam * Methods and Computer Codes for Burn-Up and Fast Transients Calculations in Subcritical Systems with External Sources * New Model of Calculation of Fission Product Yields for the ADTT Problem * Monte Carlo Simulation of Accelerator-Reactor Systems * III. Data Basis for Transmutation of Actinides and Fission Products * Nuclear Data in the Accelerator Driven Transmutation Problem * Nuclear Data to Study Radiation Damage, Activation, and Transmutation of Materials Irradiated by Particles of Intermediate and High Energies * Radium Institute Investigations on the Intermediate Energy Nuclear Data on Hybrid Nuclear Technologies * Nuclear Data Requirements in Intermediate Energy Range for Improvement of Calculations of ADTT Target Processes * IV. Experimental Studies and Projects * ADTT Experiments at the Los Alamos Neutron Science Center * Neutron Multiplicity Distributions for GeV Proton Induced Spallation Reactions on Thin and Thick Targets of Pb and U * Solid State Nuclear Track Detector and

  9. Utilization of Minor Actinides (Np, Am, Cm) in Nuclear Power Reactor

    Science.gov (United States)

    Gerasimov, A.; Bergelson, B.; Tikhomirov, G.

    2014-06-01

    Calculation research of the utilization process of minor actinides (transmutation with use of power released) is performed for specialized power reactor of the VVER type operating on the level of electric power of 1000 MW. Five subsequent cycles are considered for the reactor with fuel elements containing minor actinides along with enriched uranium. It was shown that one specialized reactor for the one cycle (900 days) can utilize minor actinides from several VVER-1000 reactors without any technological and structural modifications. Power released because of minor actinide fission is about 4% with respect to the total power

  10. FCRD Advanced Reactor (Transmutation) Fuels Handbook

    Energy Technology Data Exchange (ETDEWEB)

    Janney, Dawn Elizabeth [Idaho National Lab. (INL), Idaho Falls, ID (United States); Papesch, Cynthia Ann [Idaho National Lab. (INL), Idaho Falls, ID (United States)

    2016-09-01

    Transmutation of minor actinides such as Np, Am, and Cm in spent nuclear fuel is of international interest because of its potential for reducing the long-term health and safety hazards caused by the radioactivity of the spent fuel. One important approach to transmutation (currently being pursued by the DOE Fuel Cycle Research & Development Advanced Fuels Campaign) involves incorporating the minor actinides into U-Pu-Zr alloys, which can be used as fuel in fast reactors. U-Pu-Zr alloys are well suited for electrolytic refining, which leads to incorporation rare-earth fission products such as La, Ce, Pr, and Nd. It is, therefore, important to understand not only the properties of U-Pu-Zr alloys but also those of U-Pu-Zr alloys with concentrations of minor actinides (Np, Am) and rare-earth elements (La, Ce, Pr, and Nd) similar to those in reprocessed fuel. In addition to requiring extensive safety precautions, alloys containing U, Pu, and minor actinides (Np and Am) are difficult to study for numerous reasons, including their complex phase transformations, characteristically sluggish phasetransformation kinetics, tendency to produce experimental results that vary depending on the histories of individual samples, rapid oxidation, and sensitivity to contaminants such as oxygen in concentrations below a hundred parts per million. Although less toxic, rare-earth elements such as La, Ce, Pr, and Nd are also difficult to study for similar reasons. Many of the experimental measurements were made before 1980, and the level of documentation for experimental methods and results varies widely. It is, therefore, not surprising that little is known with certainty about U-Pu-Zr alloys, particularly those that also contain minor actinides and rare-earth elements. General acceptance of results commonly indicates that there is only a single measurement for a particular property. This handbook summarizes currently available information about U, Pu, Zr, Np, Am, La, Ce, Pr, and Nd and

  11. The value of helium-cooled reactor technologies for transmutation of nuclear waste

    Energy Technology Data Exchange (ETDEWEB)

    Rodriguez, C.; Baxter, A. [General Atomics, Los Alamos, NM (United States)

    2001-07-01

    Helium-cooled reactor technologies offer significant advantages in accomplishing the waste transmutation process. They are ideally suited for use with thermal, epithermal, or fast neutron energy spectra. They can provide a relatively hard thermal neutron spectrum for transmutation of fissionable materials such as Pu-239 using ceramic-coated transmutation fuel particles, a graphite moderator, and a non-fertile burnable poison. These features (1) allow deep levels of transmutation with minimal or no intermediate reprocessing, (2) enhance passive decay heat removal via heat conduction and radiation, (3) allow operation at relatively high temperatures for a highly efficient generation of electricity, and (4) discharge the transmuted waste in a form that is highly resistant to corrosion for long times. They also offer the possibility for the use of epithermal neutrons that can interact with transmutable materials more effectively because of the large atomic cross sections in this energy domain. A fast spectrum may be useful for deep burnup of certain minor actinides. For this application, helium is essentially transparent to neutrons, does not degrade neutron energies, and offers the hardest possible neutron energy environment. In this paper, we report results from recent work on materials transmutation balances, safety, value to a geological repository, and economic considerations. (authors)

  12. Application of gaseous core reactors for transmutation of nuclear waste

    Science.gov (United States)

    Schnitzler, B. G.; Paternoster, R. R.; Schneider, R. T.

    1976-01-01

    An acceptable management scheme for high-level radioactive waste is vital to the nuclear industry. The hazard potential of the trans-uranic actinides and of key fission products is high due to their nuclear activity and/or chemical toxicity. Of particular concern are the very long-lived nuclides whose hazard potential remains high for hundreds of thousands of years. Neutron induced transmutation offers a promising technique for the treatment of problem wastes. Transmutation is unique as a waste management scheme in that it offers the potential for "destruction" of the hazardous nuclides by conversion to non-hazardous or more manageable nuclides. The transmutation potential of a thermal spectrum uranium hexafluoride fueled cavity reactor was examined. Initial studies focused on a heavy water moderated cavity reactor fueled with 5% enriched U-235-F6 and operating with an average thermal flux of 6 times 10 to the 14th power neutrons/sq cm-sec. The isotopes considered for transmutation were I-129, Am-241, Am-242m, Am-243, Cm-243, Cm-244, Cm-245, and Cm-246.

  13. Application of gaseous core reactors for transmutation of nuclear waste

    Science.gov (United States)

    Schnitzler, B. G.; Paternoster, R. R.; Schneider, R. T.

    1976-01-01

    An acceptable management scheme for high-level radioactive waste is vital to the nuclear industry. The hazard potential of the trans-uranic actinides and of key fission products is high due to their nuclear activity and/or chemical toxicity. Of particular concern are the very long-lived nuclides whose hazard potential remains high for hundreds of thousands of years. Neutron induced transmutation offers a promising technique for the treatment of problem wastes. Transmutation is unique as a waste management scheme in that it offers the potential for "destruction" of the hazardous nuclides by conversion to non-hazardous or more manageable nuclides. The transmutation potential of a thermal spectrum uranium hexafluoride fueled cavity reactor was examined. Initial studies focused on a heavy water moderated cavity reactor fueled with 5% enriched U-235-F6 and operating with an average thermal flux of 6 times 10 to the 14th power neutrons/sq cm-sec. The isotopes considered for transmutation were I-129, Am-241, Am-242m, Am-243, Cm-243, Cm-244, Cm-245, and Cm-246.

  14. FEASIBILITY OF RECYCLING PLUTONIUM AND MINOR ACTINIDES IN LIGHT WATER REACTORS USING HYDRIDE FUEL

    Energy Technology Data Exchange (ETDEWEB)

    Greenspan, Ehud; Todreas, Neil; Taiwo, Temitope

    2009-03-10

    The objective of this DOE NERI program sponsored project was to assess the feasibility of improving the plutonium (Pu) and minor actinide (MA) recycling capabilities of pressurized water reactors (PWRs) by using hydride instead of oxide fuels. There are four general parts to this assessment: 1) Identifying promising hydride fuel assembly designs for recycling Pu and MAs in PWRs 2) Performing a comprehensive systems analysis that compares the fuel cycle characteristics of Pu and MA recycling in PWRs using the promising hydride fuel assembly designs identified in Part 1 versus using oxide fuel assembly designs 3) Conducting a safety analysis to assess the likelihood of licensing hydride fuel assembly designs 4) Assessing the compatibility of hydride fuel with cladding materials and water under typical PWR operating conditions Hydride fuel was found to offer promising transmutation characteristics and is recommended for further examination as a possible preferred option for recycling plutonium in PWRs.

  15. Fuel and target programs for the transmutation at Phenix and other reactors; Programmes combustibles et cibles pour la transmutation dans Phenix et autres reacteurs

    Energy Technology Data Exchange (ETDEWEB)

    Gaillard-Groleas, G

    2002-07-01

    The fuels and targets program for transmutation, performed in the framework of the axis 1 of the December 1991 law about the researches on the management of long-lived radioactive wastes, is in perfect consistency with the transmutation scenario studies carried out in the same framework. These studies put forward the advantage of fast breeder reactors (FBR) in the incineration of minor actinides and long-lived fission products. The program includes exploratory and technological demonstration studies covering the different design options. It aims at enhancing our knowledge of the behaviour of materials under irradiation and at ensuring the mastery of processes. The goals of the different experiments foreseen at Phenix reactor are presented. The main goal is to supply a set of results allowing to precise the conditions of the technical feasibility of minor actinides and long-lived fission products incineration in FBRs. (J.S.)

  16. Status of nuclear data for actinides

    Energy Technology Data Exchange (ETDEWEB)

    Guzhovskii, B.Y.; Gorelov, V.P.; Grebennikov, A.N. [Russia Federal Nuclear Centre, Arzamas (Russian Federation)] [and others

    1995-10-01

    Nuclear data required for transmutation problem include many actinide nuclei. In present paper the analysis of neutron fission, capture, (n,2n) and (n,3n) reaction cross sections at energy region from thermal point to 14 MeV was carried out for Th, Pa, U, Np, Pu, Am and Cm isotops using modern evaluated nuclear data libraries and handbooks of recommended nuclear data. Comparison of these data indicates on substantial discrepancies in different versions of files, that connect with quality and completeness of original experimental data.

  17. ACCELERATOR TRANSMUTATION OF WASTE TECHNOLOGY AND IMPLEMENTATION SCENARIOS

    Energy Technology Data Exchange (ETDEWEB)

    D. BELLER; G. VAN TUYLE

    2000-11-01

    During 1999, the U.S. Department of Energy, in conjunction with its nuclear laboratories, a national steering committee, and a panel of world experts, developed a roadmap for research, development, demonstration, and deployment of Accelerator-driven Transmutation of Waste (ATW). The ATW concept that was examined in this roadmap study was based on that developed at the Los Alamos National Laboratory (LANL) during the 1990s. The reference deployment scenario in the Roadmap was developed to treat 86,300 tn (metric tonnes initial heavy metal) of spent nuclear fuel that will accumulate through 2035 from existing U.S. nuclear power plants (without license extensions). The disposition of this spent nuclear reactor fuel is an issue of national importance, as is disposition of spent fuel in other nations. The U.S. program for the disposition of this once-through fuel is focused to characterize a candidate site at Yucca Mountain, Nevada for a geological repository for spent fuel and high-level waste. The ATW concept is being examined in the U.S. because removal of plutonium minor actinides, and two very long-lived isotopes from the spent fuel can achieve some important objectives. These objectives include near-elimination of plutonium, reduction of the inventory and mobility of long-lived radionuclides in the repository, and use of the remaining energy content of the spent fuel to produce power. The long-lived radionuclides iodine and technetium have roughly one million year half-lives, and they are candidates for transport into the environment via movement of ground water. The scientists and engineers who contributed to the Roadmap Study determined that the ATW is affordable, doable, and its deployment would support all the objectives. We report the status of the U.S. ATW program describe baseline and alternate technologies, and discuss deployment scenarios to support the existing U.S. nuclear capability and/or future growth with a variety of new fuel cycles.

  18. GCFR Coupled Neutronic and Thermal-Fluid-Dynamics Analyses for a Core Containing Minor Actinides

    Directory of Open Access Journals (Sweden)

    Diego Castelliti

    2009-01-01

    Full Text Available Problems about future energy availability, climate changes, and air quality seem to play an important role in energy production. While current reactor generations provide a guaranteed and economical energy production, new nuclear power plant generation would increase the ways and purposes in which nuclear energy can be used. To explore these new technological applications, several governments, industries, and research communities decided to contribute to the next reactor generation, called “Generation IV.” Among the six Gen-IV reactor designs, the Gas Cooled Fast Reactor (GCFR uses a direct-cycle helium turbine for electricity generation and for a CO2-free thermochemical production of hydrogen. Additionally, the use of a fast spectrum allows actinides transmutation, minimizing the production of long-lived radioactive waste in an integrated fuel cycle. This paper presents an analysis of GCFR fuel cycle optimization and of a thermal-hydraulic of a GCFR-prototype under steady-state and transient conditions. The fuel cycle optimization was performed to assess the capability of the GCFR to transmute MAs, while the thermal-hydraulic analysis was performed to investigate the reactor and the safety systems behavior during a LOFA. Preliminary results show that limited quantities of MA are not affecting significantly the thermal-fluid-dynamics behavior of a GCFR core.

  19. Electrochemical reduction of CerMet fuels for transmutation using surrogate CeO2-Mo pellets

    Science.gov (United States)

    Claux, B.; Souček, P.; Malmbeck, R.; Rodrigues, A.; Glatz, J.-P.

    2017-08-01

    One of the concepts chosen for the transmutation of minor actinides in Accelerator Driven Systems or fast reactors proposes the use of fuels and targets containing minor actinides oxides embedded in an inert matrix either composed of molybdenum metal (CerMet fuel) or of ceramic magnesium oxide (CerCer fuel). Since the sufficient transmutation cannot be achieved in a single step, it requires multi-recycling of the fuel including recovery of the not transmuted minor actinides. In the present work, a pyrochemical process for treatment of Mo metal inert matrix based CerMet fuels is studied, particularly the electroreduction in molten chloride salt as a head-end step required prior the main separation process. At the initial stage, different inactive pellets simulating the fuel containing CeO2 as minor actinide surrogates were examined. The main studied parameters of the process efficiency were the porosity and composition of the pellets and the process parameters as current density and passed charge. The results indicated the feasibility of the process, gave insight into its limiting parameters and defined the parameters for the future experiment on minor actinide containing material.

  20. Neutronic Analysis and Transmutation Performance of Th-based Molten Salt Fuels

    Energy Technology Data Exchange (ETDEWEB)

    Bak, Sangin; Chai, Jongseo; Hong, Seungwoo; Kadi, Yacine; Tenreiro, Claudio [Department of Energy Science/SungKyunKwan Univ., Suwon (Korea, Republic of); Curbelo, Jesus Perez [Higher Institute of Technologies and Applied Sciences, Havana (Chad); Kadi, Yacine [Engineering Department/European Organization for Nuclear Research, Geneva (Swaziland); Tenreiro, Claudio [Faculty of Engineering/Univ. of Talca, Talca (Chile)

    2013-05-15

    The utilization of thorium in various reactors ranging from thermal to fast neutron energies has been successfully demonstrated, but substantial R and D is required before commercialization becomes possible. The molten-salt reactor (MSR) systems present the very special feature of a liquid fuel. MSR concepts, which can be used as efficient burners of TRU from spent LWR fuel, have also a breeding capability in any kind of neutron spectrum (from thermal to fast), when using the thorium fuel cycle. It has a very interesting potential for the minimization of radio toxic nuclear waste. For a pure Th-U fuel, thermal/epithermal molten salt is better than a fast one. The system has better breeding ratio and can reach k{sub eff} with smaller enrichment than fast system, because of the neutron leakage of the fast system. However the fast fuel salts is preferred for the transmutation of Minor Actinides. When mixed with MA and Pu, thorium based fast molten salts have similar breeding capability as thermal/epithermal salts.

  1. The role of Z-pinch fusion transmutation of waste in the nuclear fuel cycle.

    Energy Technology Data Exchange (ETDEWEB)

    Smith, James Dean; Drennen, Thomas E. (Hobart & William Smith College, Geneva, NY); Rochau, Gary Eugene; Martin, William Joseph; Kamery, William (Hobart & William Smith College, Geneva, NY); Phruksarojanakun, Phiphat (University of Wisconsin, Madison, WI); Grady, Ryan (University of Wisconsin, Madison, WI); Cipiti, Benjamin B.; Wilson, Paul Philip Hood (University of Wisconsin, Madison, WI); Mehlhorn, Thomas Alan; Guild-Bingham, Avery (Texas A& M University, College Station, TX); Tsvetkov, Pavel Valeryevich (Texas A& M University, College Station, TX)

    2007-10-01

    The resurgence of interest in reprocessing in the United States with the Global Nuclear Energy Partnership has led to a renewed look at technologies for transmuting nuclear waste. Sandia National Laboratories has been investigating the use of a Z-Pinch fusion driver to burn actinide waste in a sub-critical reactor. The baseline design has been modified to solve some of the engineering issues that were identified in the first year of work, including neutron damage and fuel heating. An on-line control feature was added to the reactor to maintain a constant neutron multiplication with time. The transmutation modeling effort has been optimized to produce more accurate results. In addition, more attention was focused on the integration of this burner option within the fuel cycle including an investigation of overall costs. This report presents the updated reactor design, which is able to burn 1320 kg of actinides per year while producing 3,000 MWth.

  2. Analysis of advanced european nuclear fuel cycle scenarios including transmutation and economical estimates

    Energy Technology Data Exchange (ETDEWEB)

    Merino Rodriguez, I.; Alvarez-Velarde, F.; Martin-Fuertes, F. [CIEMAT, Avda. Complutense, 40, 28040 Madrid (Spain)

    2013-07-01

    In this work the transition from the existing Light Water Reactors (LWR) to the advanced reactors is analyzed, including Generation III+ reactors in a European framework. Four European fuel cycle scenarios involving transmutation options have been addressed. The first scenario (i.e., reference) is the current fleet using LWR technology and open fuel cycle. The second scenario assumes a full replacement of the initial fleet with Fast Reactors (FR) burning U-Pu MOX fuel. The third scenario is a modification of the second one introducing Minor Actinide (MA) transmutation in a fraction of the FR fleet. Finally, in the fourth scenario, the LWR fleet is replaced using FR with MOX fuel as well as Accelerator Driven Systems (ADS) for MA transmutation. All scenarios consider an intermediate period of GEN-III+ LWR deployment and they extend for a period of 200 years looking for equilibrium mass flows. The simulations were made using the TR-EVOL code, a tool for fuel cycle studies developed by CIEMAT. The results reveal that all scenarios are feasible according to nuclear resources demand (U and Pu). Concerning to no transmutation cases, the second scenario reduces considerably the Pu inventory in repositories compared to the reference scenario, although the MA inventory increases. The transmutation scenarios show that elimination of the LWR MA legacy requires on one hand a maximum of 33% fraction (i.e., a peak value of 26 FR units) of the FR fleet dedicated to transmutation (MA in MOX fuel, homogeneous transmutation). On the other hand a maximum number of ADS plants accounting for 5% of electricity generation are predicted in the fourth scenario (i.e., 35 ADS units). Regarding the economic analysis, the estimations show an increase of LCOE (Levelized cost of electricity) - averaged over the whole period - with respect to the reference scenario of 21% and 29% for FR and FR with transmutation scenarios respectively, and 34% for the fourth scenario. (authors)

  3. Transmutation of Nuclear Waste and the future MYRRHA Demonstrator

    CERN Document Server

    Mueller, Alex C

    2012-01-01

    While a considerable and world-wide growth of the nuclear share in the global energy mix is desirable for many reasons, there are also, in particular in the "old world" major objections. These are both concerns about safety, in particular in the wake of the Fukushima nuclear accident and concerns about the long-term burden that is constituted by the radiotoxic waste from the spent fuel. With regard to the second topic, the present contribution will outline the concept of Partitioning & Transmutation (P&T), as scientific and technological answer. Deployment of P&T may use dedicated "Transmuter" or "Burner" reactors, using a fast neutron spectrum. For the transmutation of waste with a large content (up to 50%) of (very long-lived) Minor Actinides, a sub-critical reactor, using an external neutron source is a most attractive solution. It is constituted by coupling a proton accelerator, a spallation target and a subcritical core. This promising new technology is named ADS, for accelerator-driven syste...

  4. Application of variance reduction technique to nuclear transmutation system driven by accelerator

    Energy Technology Data Exchange (ETDEWEB)

    Sasa, Toshinobu [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    1998-03-01

    In Japan, it is the basic policy to dispose the high level radioactive waste arising from spent nuclear fuel in stable deep strata after glass solidification. If the useful elements in the waste can be separated and utilized, resources are effectively used, and it can be expected to guarantee high economical efficiency and safety in the disposal in strata. Japan Atomic Energy Research Institute proposed the hybrid type transmutation system, in which high intensity proton accelerator and subcritical fast core are combined, or the nuclear reactor which is optimized for the exclusive use for transmutation. The tungsten target, minor actinide nitride fuel transmutation system and the melted minor actinide chloride salt target fuel transmutation system are outlined. The conceptual figures of both systems are shown. As the method of analysis, Version 2.70 of Lahet Code System which was developed by Los Alamos National Laboratory in USA was adopted. In case of carrying out the analysis of accelerator-driven subcritical core in the energy range below 20 MeV, variance reduction technique must be applied. (K.I.)

  5. MA Transmutation Strategy%MA嬗变策略研究

    Institute of Scientific and Technical Information of China (English)

    左国平; 柯国土; 龚学余

    2011-01-01

    According to the development plan envisagement for nuclear power plant in China, the development of China's nuclear power in the next decades is predicted with the. nuclear fuel cycle software NFCSS provided by IAEA. The amounts of the spent fuel generated and accumulated by the year of 2050 are analyzed. According to the assumption model, the accumulated spent fuel by the year of 2050 will reach at 54791t including 57.89t Minor Actinides (MA) (237Np, 42.91t; Am, ll.17t; Cm, 3.81t) and 2778t FP. One group effective cross section of MA in the thermal, well thermalized, and fast neutron field is calculated based on ENDF/B-VII nuclear evaluation database. The transmutation way for three main MA, i.e. 237Np, 241Am, and 246Cm is also analyzed. It is more suitable for 237Np transmutation in well thermalized neutron field and for 241Am, the high flux thermalized neutron field is better. But it is difficult for 246Cm transmutation in thermal or fast neutron field due to its little fission cross section. Its transmutation ability can be improved if transmutation occurs in a high fluxes resonance energy area. The two-stage transmutation strategy is presented according to their characteristics in the thermal, well thermalized, and fast neutron field. Based on the two stage transmutation concept, the transmutation is performed in a well thermalized neutron field first. Small amount of residual of the first stage transmutation is transmuted in a thermal field with a spectrum. It is expected to achieve a good result.%根据中国核电发展战略,采用国际原子能机构(IAEA)的核燃料循环软件NFCSS,对未来中国核电发展情景进行了预测,分析了2050年以前中国乏燃料的产生和累积情况.采用NJOY和ENDF/B-VII数据库,计算分析了次锕系核素在热谱、超热谱和快谱中的一群等效截面,分析了研237Np、241Am、246Cm等主要次锕系核素的可能嬗变途径,提出了两阶段嬗变MA策略.即将从压水堆中分离出来

  6. Partitioning and Transmutation. Annual Report 2002

    Energy Technology Data Exchange (ETDEWEB)

    Andersson, S.; Ekberg, C.; Liljenzin, J.O.; Nilsson, M.; Rogues, N.; Skarnemark, G.; Oestberg, J. [Chalmers Univ. of Tech., Goeteborg (Sweden). Dept. of Materials and Surface Chemistry

    2003-01-01

    How to deal with the spent fuel from nuclear power plants is an issue that much research is attracted to in many countries around the world. Several different strategies exist for treating the waste ranging from direct disposal to reprocessing and recycling of plutonium and other long-lived nuclides. In either case the remains have to be stored for a long time to render it radio-toxically safe. One method to deal with this long-lived waste is to separate (separation) out the most long lived components and then transform them into shorter-lived ones (transmutation). Several methods exist for performing the separation for example via molten salts and through solvent extraction. The work presented here has been focused on solvent extraction. This technique is well known since many years and process scale plants have been operating for decades. The new demand is to separate chemically very similar elements from each other. Within this project this is done by new extracting agents developed for this purpose alone within the EU fifth framework programme, the PARTNEW project, particularly from the University of Reading. In this work we investigate different extraction systems for the separation of trivalent actinides from trivalent lanthanides using extraction agents following the so-called CHON (Carbon, Hydrogen, Oxygen and Nitrogen) principle. The main focus is to understand the basic chemistry involved but also some processing behaviour for use in future full scale plants.

  7. Actinides reduction by recycling in a thermal reactor; Reduccion de actinidos por reciclado en un reactor termico

    Energy Technology Data Exchange (ETDEWEB)

    Ramirez S, J. R.; Martinez C, E.; Balboa L, H., E-mail: ramon.ramirez@inin.gob.mx [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

    2014-10-15

    This work is directed towards the evaluation of an advanced nuclear fuel cycle in which radioactive actinides could be recycled to remove most of the radioactive material; firstly a production reference of actinides in standard nuclear fuel of uranium at the end of its burning in a BWR reactor is established, after a fuel containing plutonium is modeled to also calculate the actinides production in MOX fuel type. Also it proposes a design of fuel rod containing 6% of actinides in a matrix of uranium from the tails of enrichment, then four standard uranium fuel rods are replaced by actinides rods to evaluate the production and transmutation thereof, the same procedure was performed in the fuel type MOX and the end actinide reduction in the fuel was evaluated. (Author)

  8. Selective Separation of Trivalent Actinides from Lanthanides by Aqueous Processing with Introduction of Soft Donor Atoms

    Energy Technology Data Exchange (ETDEWEB)

    Kenneth L. Nash

    2009-09-22

    Implementation of a closed loop nuclear fuel cycle requires the utilization of Pu-containing MOX fuels with the important side effect of increased production of the transplutonium actinides, most importantly isotopes of Am and Cm. Because the presence of these isotopes significantly impacts the long-term radiotoxicity of high level waste, it is important that effective methods for their isolation and/or transmutation be developed. Furthermore, since transmutation is most efficiently done in the absence of lanthanide fission products (high yield species with large thermal neutron absorption cross sections) it is important to have efficient procedures for the mutual separation of Am and Cm from the lanthanides. The chemistries of these elements are nearly identical, differing only in the slightly stronger strength of interaction of trivalent actinides with ligand donor atoms softer than O (N, Cl-, S). Research being conducted around the world has led to the development of new reagents and processes with considerable potential for this task. However, pilot scale testing of these reagents and processes has demonstrated the susceptibility of the new classes of reagents to radiolytic and hydrolytic degradation. In this project, separations of trivalent actinides from fission product lanthanides have been investigated in studies of 1) the extraction and chemical stability properties of a class of soft-donor extractants that are adapted from water-soluble analogs, 2) the application of water soluble soft-donor complexing agents in tandem with conventional extractant molecules emphasizing fundamental studies of the TALSPEAK Process. This research was conducted principally in radiochemistry laboratories at Washington State University. Collaborators at the Radiological Processing Laboratory (RPL) at the Pacific Northwest National Laboratory (PNNL) have contributed their unique facilities and capabilities, and have supported student internships at PNNL to broaden their

  9. Selective Separation of Trivalent Actinides from Lanthanides by Aqueous Processing with Introduction of Soft Donor Atoms

    Energy Technology Data Exchange (ETDEWEB)

    Kenneth L. Nash

    2009-09-22

    Implementation of a closed loop nuclear fuel cycle requires the utilization of Pu-containing MOX fuels with the important side effect of increased production of the transplutonium actinides, most importantly isotopes of Am and Cm. Because the presence of these isotopes significantly impacts the long-term radiotoxicity of high level waste, it is important that effective methods for their isolation and/or transmutation be developed. Furthermore, since transmutation is most efficiently done in the absence of lanthanide fission products (high yield species with large thermal neutron absorption cross sections) it is important to have efficient procedures for the mutual separation of Am and Cm from the lanthanides. The chemistries of these elements are nearly identical, differing only in the slightly stronger strength of interaction of trivalent actinides with ligand donor atoms softer than O (N, Cl-, S). Research being conducted around the world has led to the development of new reagents and processes with considerable potential for this task. However, pilot scale testing of these reagents and processes has demonstrated the susceptibility of the new classes of reagents to radiolytic and hydrolytic degradation. In this project, separations of trivalent actinides from fission product lanthanides have been investigated in studies of 1) the extraction and chemical stability properties of a class of soft-donor extractants that are adapted from water-soluble analogs, 2) the application of water soluble soft-donor complexing agents in tandem with conventional extractant molecules emphasizing fundamental studies of the TALSPEAK Process. This research was conducted principally in radiochemistry laboratories at Washington State University. Collaborators at the Radiological Processing Laboratory (RPL) at the Pacific Northwest National Laboratory (PNNL) have contributed their unique facilities and capabilities, and have supported student internships at PNNL to broaden their

  10. Partitioning and Transmutation - Annual Report 2010 and 2011

    Energy Technology Data Exchange (ETDEWEB)

    Aneheim, Emma; Ekberg, Christian; Fermvik, Anna; Foreman, Mark; Littley, Alexander; Loefstroem-Engdahl, Elin; Mabile, Nathalie; Skarnemark, Gunnar [Nuclear Chemistry, Dept. of Chemical and Biological Engineering, Chalmers Univ. of Technology, Goeteborg (Sweden)

    2013-01-15

    The long-lived elements in the spent nuclear fuels are mostly actinides, some fission products ({sup 79}Se, {sup 87}Rb, {sup 99}Tc, {sup 107}Pd, {sup 126}Sn, {sup 129}I and {sup 135}Cs) and activation products ({sup 14}C, {sup 36}Cl, {sup 59}Ni, {sup 93}Zr, {sup 94}Nb). To be able to destroy the long-lived elements in a transmutation process they must be separated from the rest of the spent nuclear fuel for different reasons. One being high neutron capture cross-sections for some elements, like the lanthanides. Other reasons may be the unintentional production of other long lived isotopes. The most difficult separations to make are those between different actinides but also between trivalent actinides and lanthanides, due to their relatively similar chemical properties. Solvent extraction is an efficient and well-known method that makes it possible to have separation factors that fulfil the highly set demands on purity of the separated phases and on small losses. In the case of a fuel with a higher burnup or possible future fuels, pyro processing may be of higher advantage due to the limited risk of criticality during the process. Chalmers University of Technology is involved in research regarding the separation of actinides and lanthanides and between the actinides themselves as a partner in several European frame work programmes. These projects have ranged from NEWPART in the 4th framework via PARTNEW and EUROPART to ACSEPT in the present 7th programme. The aims of the projects have now shifted from basic understanding to more applied research with focus on process development. One recycling route, called DIAMEX (DIAmide EXtracton) / SANEX (Selective ActiNide EXtraction) is now considered to be working on a basic scale and has been proven in hot tests and focus has moved on to more process oriented areas. However, since further investigations on basic understanding of the chemical behavior are required, we have our main focus on the chemical processes and

  11. A compact Tokamak transmutation reactor

    Institute of Scientific and Technical Information of China (English)

    QiuLi-Jian; XiaoBing-Jia

    1997-01-01

    The low aspect ration tokamak is proposed for the driver of a transmutation reactor.The main parameters of the reactor core,neutronic analysis of the blanket are given>the neutron wall loading can be lowered from the magnitude order of 1 MW/m2 to 0.5MW/m2 which is much easier to reach in the near future,and the transmutation efficiency (fission/absorption ratio)is raised further.The blanket power density is about 200MW/m3 which is not difficult to deal with.The key components such as diverter and center conductor post are also designed and compared with conventional TOkamak,Finally,by comparison with the other drivers such as FBR,PWR and accelerator,it can be anticipated that the low aspect ratio transmutation reactor would be one way of fusion energy applications in the near future.

  12. Transmuted Complementary Weibull Geometric Distribution

    Directory of Open Access Journals (Sweden)

    Ahmed Z. A…fify

    2014-12-01

    Full Text Available This paper provides a new generalization of the complementary Weibull geometric distribution that introduced by Tojeiro et al. (2014, using the quadratic rank transmutation map studied by Shaw and Buckley (2007. The new distribution is referred to as transmuted complementary Weibull geometric distribution (TCWGD. The TCWG distribution includes as special cases the complementary Weibull geometric distribution (CWGD, complementary exponential geometric distribution(CEGD,Weibull distribution (WD and exponential distribution (ED. Various structural properties of the new distribution including moments, quantiles, moment generating function and RØnyi entropy of the subject distribution are derived. We proposed the method of maximum likelihood for estimating the model parameters and obtain the observed information matrix. A real data set are used to compare the ‡exibility of the transmuted version versus the complementary Weibull geometric distribution.

  13. Fabrication and Pre-irradiation Characterization of a Minor Actinide and Rare Earth Containing Fast Reactor Fuel Experiment for Irradiation in the Advanced Test Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Timothy A. Hyde

    2012-06-01

    The United States Department of Energy, seeks to develop and demonstrate the technologies needed to transmute the long-lived transuranic actinide isotopes contained in spent nuclear fuel into shorter lived fission products, thereby decreasing the volume of material requiring disposal and reducing the long-term radiotoxicity and heat load of high-level waste sent to a geologic repository. This transmutation of the long lived actinides plutonium, neptunium, americium and curium can be accomplished by first separating them from spent Light Water Reactor fuel using a pyro-metalurgical process, then reprocessing them into new fuel with fresh uranium additions, and then transmuted to short lived nuclides in a liquid metal cooled fast reactor. An important component of the technology is developing actinide-bearing fuel forms containing plutonium, neptunium, americium and curium isotopes that meet the stringent requirements of reactor fuels and materials.

  14. AFC-1 Transmutation Fuels Post-Irradiation Hot Cell Examination 4-8 at.% - Final Report (Irradiation Experiments AFC-1B, -1F and -1Æ)

    Energy Technology Data Exchange (ETDEWEB)

    Bruce Hilton; Douglas Porter; Steven Hayes

    2006-09-01

    The AFC-1B, AFC-1F and AFC-1Æ irradiation tests are part of a series of test irradiations designed to evaluate the feasibility of the use of actinide bearing fuel forms in advanced fuel cycles for the transmutation of transuranic elements from nuclear waste. The tests were irradiated in the Idaho National Laboratory’s (INL) Advanced Test Reactor (ATR) to an intermediate burnup of 4 to 8 at% (2.7 - 6.8 x 1020 fiss/cm3). The tests contain metallic and nitride fuel forms with non-fertile (i.e., no uranium) and low-fertile (i.e., uranium bearing) compositions. Results of postirradiation hot cell examinations of AFC-1 irradiation tests are reported for eleven metallic alloy transmutation fuel rodlets and five nitride transmutation fuel rodlets. Non-destructive examinations included visual examination, dimensional inspection, gamma scan analysis, and neutron radiography. Detailed examinations, including fission gas puncture and analysis, metallography / ceramography and isotopics and burnup analyses, were performed on five metallic alloy and three nitride transmutation fuels. Fuel performance of both metallic alloy and nitride fuel forms was best correlated with fission density as a burnup metric rather than at.% depletion. The actinide bearing transmutation metallic alloy compositions exhibit irradiation performance very similar to U-xPu-10Zr fuel at equivalent fission densities. The irradiation performance of nitride transmutation fuels was comparable to limited data published on mixed nitride systems.

  15. Actinide Isotopes for the Synthesis of Superheavy Nuclei

    Science.gov (United States)

    Roberto, J. B.; Alexander, C. W.; Boll, R. A.; Dean, D. J.; Ezold, J. G.; Felker, L. K.; Rykaczewski, K. P.

    2014-09-01

    Recent research resulting in the synthesis of isotopes of new elements 113-118 has demonstrated the importance of actinide targets in superheavy element research. Oak Ridge National Laboratory (ORNL) has unique facilities for the production and processing of actinide target materials, including the High Flux Isotope Reactor (HFIR) and the Radiochemical Engineering Development Center (REDC). These facilities have provided actinide target materials that have been used for the synthesis of all superheavy (SHE) elements above Copernicium (element 112). In this paper, the use of actinide targets for SHE research and discovery is described, including recent results for element 117 using 249Bk target material from ORNL. ORNL actinide capabilities are reviewed, including production and separation/purification, availabilities of actinide materials, and future opportunities including novel target materials such as 251Cf.

  16. Transmutation of present transuranics elements in the fuel nuclear radiated; Transmutacion de elementos transuranicos presentes en los combustible nucleares irradiados

    Energy Technology Data Exchange (ETDEWEB)

    Gonzalez, E.; Alvarez, F.; Blazquez, J.; Cano-Ott, D.; Fernandez Ordonez, M.; Guerrero, C.; Martin-Fuertes, F.; Martinez, T.; Vicente, C.; Villamarin, D.

    2008-07-01

    This technical report of ENRESA refers to the transmutation of some transuranic elements, mainly plutonium and minor actinides (Np, Am and Cm). The transmutation of minor actinides (MA) could be efficiently made by very energetic neutrons, using fast reactors of Generation IV or accelerator driven systems (ADS). This publication is dedicated to expose the state-of-the-art situation of the ADS, mainly the activities developed by CIEMAT within the R+D projects of the EU. This technical publication of ENRESA on Transmutation is the second volume, of a set of two, on Partitioning and Transmutation. The first volume, entitled Partitioning of transuranic elements and some fission products from spent nuclear fuels, was published in 2006. The present report has ten chapters; the first one is an introduction on the spent fuels management, mainly in Spain. In the second one a summary of the main characteristics of spent fuels is provided; in the third the transmutation concept including their nuclear reactions is described; and in the fourth one a description of the present management options of the spent fuels is given. In the fifth chapter several new advanced closed cycles with transmutation of Pu and MA are given and in the sixth one the main proposed transmutation systems are de scribed. Among these, a great emphasis is given to the ADS including its main parts, as they are: the proton accelerator, the spallation source for neutrons production and the subcritical core. Also a re view of different fuels and proposed cool ants for the ADS is made, as well as proposed reprocessing of the transmuted spent fuel from ADS. In this chapter a description of some R+D projects is given, most of them supported by the European Union, with participation of CIEMAT. Chapters seven and eight show the progress on the measurement of new nuclear data to complete the simulation of the transmutation basic processes and systems, together in chapter nine with new R+D activities on

  17. Accelerator-driven transmutation reactor analysis code system (ATRAS)

    Energy Technology Data Exchange (ETDEWEB)

    Sasa, Toshinobu; Tsujimoto, Kazufumi; Takizuka, Takakazu; Takano, Hideki [Japan Atomic Energy Research Inst., Tokai, Ibaraki (Japan). Tokai Research Establishment

    1999-03-01

    JAERI is proceeding a design study of the hybrid type minor actinide transmutation system which mainly consist of an intense proton accelerator and a fast subcritical core. Neutronics and burnup characteristics of the accelerator-driven system is important from a view point of the maintenance of subcriticality and energy balance during the system operation. To determine those characteristics accurately, it is necessary to involve reactions at high-energy region, which are not treated on ordinary reactor analysis codes. The authors developed a code system named ATRAS to analyze the neutronics and burnup characteristics of accelerator-driven subcritical reactor systems. ATRAS has a function of burnup analysis taking account of the effect of spallation neutron source. ATRAS consists of a spallation analysis code, a neutron transport codes and a burnup analysis code. Utility programs for fuel exchange, pre-processing and post-processing are also incorporated. (author)

  18. Research in actinide chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Choppin, G.R.

    1993-01-01

    This research studies the behavior of the actinide elements in aqueous solution. The high radioactivity of the transuranium actinides limits the concentrations which can be studied and, consequently, limits the experimental techniques. However, oxidation state analogs (trivalent lanthanides, tetravalent thorium, and hexavalent uranium) do not suffer from these limitations. Behavior of actinides in the environment are a major USDOE concern, whether in connection with long-term releases from a repository, releases from stored defense wastes or accidental releases in reprocessing, etc. Principal goal of our research was expand the thermodynamic data base on complexation of actinides by natural ligands (e.g., OH[sup [minus

  19. Neutron transmutation doped Ge bolometers

    Science.gov (United States)

    Haller, E. E.; Kreysa, E.; Palaio, N. P.; Richards, P. L.; Rodder, M.

    1983-01-01

    Some conclusions reached are as follow. Neutron Transmutation Doping (NTD) of high quality Ge single crystals provides perfect control of doping concentration and uniformity. The resistivity can be tailored to any given bolometer operating temperature down to 0.1 K and probably lower. The excellent uniformity is advantaged for detector array development.

  20. Facilities for preparing actinide or fission product-based targets

    CERN Document Server

    Sors, M

    1999-01-01

    Research and development work is currently in progress in France on the feasibility of transmutation of very long-lived radionuclides such as americium, blended with an inert medium such as magnesium oxide and pelletized for irradiation in a fast neutron reactor. The process is primarily designed to produce ceramics for nuclear reactors, but could also be used to produce targets for accelerators. The Actinide Development Laboratory is part of the ATALANTE complex at Marcoule, where the CEA investigates reprocessing, liquid and solid waste treatment and vitrification processes. The laboratory produces radioactive sources; after use, their constituents are recycled, notably through R and D programs requiring such materials. Recovered americium is purified, characterized and transformed for an experiment known as ECRIX, designed to demonstrate the feasibility of fabricating americium-based ceramics and to determine the reactor transmutation coefficients.

  1. SACSESS – the EURATOM FP7 project on actinide separation from spent nuclear fuels

    Directory of Open Access Journals (Sweden)

    Bourg Stéphane

    2015-12-01

    Full Text Available Recycling of actinides by their separation from spent nuclear fuel, followed by transmutation in fast neutron reactors of Generation IV, is considered the most promising strategy for nuclear waste management. Closing the fuel cycle and burning long-lived actinides allows optimizing the use of natural resources and minimizing the long-term hazard of high-level nuclear waste. Moreover, improving the safety and sustainability of nuclear power worldwide. This paper presents the activities striving to meet these challenges, carried out under the Euratom FP7 collaborative project SACSESS (Safety of Actinide Separation Processes. Emphasis is put on the safety issues of fuel reprocessing and waste storage. Two types of actinide separation processes, hydrometallurgical and pyrometallurgical, are considered, as well as related aspects of material studies, process modeling and the radiolytic stability of solvent extraction systems. Education and training of young researchers in nuclear chemistry is of particular importance for further development of this field.

  2. Advanced Aqueous Separation Systems for Actinide Partitioning

    Energy Technology Data Exchange (ETDEWEB)

    Nash, Ken [Washington State Univ., Pullman, WA (United States); Martin, Leigh [Idaho National Lab. (INL), Idaho Falls, ID (United States); Lumetta, Gregg [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2015-04-02

    One of the most challenging aspects of advanced processing of used nuclear fuel is the separation of transplutonium actinides from fission product lanthanides. This separation is essential if actinide transmutation options are to be pursued in advanced fuel cycles, as lanthanides compete with actinides for neutrons in both thermal and fast reactors, thus limiting efficiency. The separation is difficult because the chemistry of Am3+ and Cm3+ is nearly identical to that of the trivalent lanthanides (Ln3+). The prior literature teaches that two approaches offer the greatest probability of devising a successful group separation process based on aqueous processes: 1) the application of complexing agents containing ligand donor atoms that are softer than oxygen (N, S, Cl-) or 2) changing the oxidation state of Am to the IV, V, or VI state to increase the essential differences between Am and lanthanide chemistry (an approach utilized in the PUREX process to selectively remove Pu4+ and UO22+ from fission products). The latter approach offers the additional benefit of enabling a separation of Am from Cm, as Cm(III) is resistant to oxidation and so can easily be made to follow the lanthanides. The fundamental limitations of these approaches are that 1) the soft(er) donor atoms that interact more strongly with actinide cations than lanthanides form substantially weaker bonds than oxygen atoms, thus necessitating modification of extraction conditions for adequate phase transfer efficiency, 2) soft donor reagents have been seen to suffer slow phase transfer kinetics and hydro-/radiolytic stability limitations and 3) the upper oxidation states of Am are all moderately strong oxidants, hence of only transient stability in media representative of conventional aqueous separations systems. There are examples in the literature of both approaches having been described. However, it is not clear at present that any extant process is sufficiently robust for application at the scale

  3. Measurements of thermal fission and capture cross sections of minor actinides within the Mini-INCA project

    Energy Technology Data Exchange (ETDEWEB)

    Bringer, O.; Chabod, S.; Dupont, E.; Letourneau, A.; Panebianco, S.; Veyssiere, Ch. [CEA Saclay, Dept. d' Astrophysique de Physique des Particules, de Physique Nucleaire et de l' Instrumentation Associee, 91- Gif sur Yvette (France); Oriol, L. [CEA Cadarache, Dept. d' Etudes des Reacteurs, 13 - Saint Paul lez Durance (France); Chartier, F. [CEA Saclay, Dept. de Physico-Chimie, 91 - Gif sur Yvette (France); Mutti, P. [Institut Laue Langevin, 38 - Grenoble, (France); AlMahamid, I. [Wadsworth Center, New York State Dept. of Health, Albany, NY (United States)

    2008-07-01

    In the framework of nuclear waste transmutation studies, the Mini-INCA project has been initiated at Cea/DSM to determine optimal conditions for transmutation and incineration of Minor Actinides in high intensity neutron fluxes in the thermal region. Our experimental tool is based on alpha- and gamma-spectroscopy of irradiated samples and microscopic fission-chambers. It can provide both microscopic information on nuclear reactions (total and partial cross sections for neutron capture and/or fission reactions) and macroscopic information on transmutation and incineration potentials. The {sup 232}Th, {sup 237}Np, {sup 241}Am, and {sup 244}Cm transmutation chains have been explored in details, showing some discrepancies in comparison with evaluated data libraries but in overall good agreement with recent experimental data. (authors)

  4. Transmutation Strategy Using Thorium-Reprocessed Fuel ADS for Future Reactors in Vietnam

    Directory of Open Access Journals (Sweden)

    Thanh Mai Vu

    2013-01-01

    Full Text Available Nuclear power is believed to be a key to the energy security for a developing country like Vietnam where the power demanding increases rapidly every year. Nevertheless, spent nuclear fuel from nuclear power plants is the source of radiotoxic and proliferation risk. A conceptual design of ADS utilizing thorium fuel as a based fuel and reprocessed fuel as a seed for nuclear waste transmutation and energy production is proposed as one of the clean, safe, and economical solutions for the problem. In the design, 96 seed assemblies and 84 blanket assemblies were inserted into the core to make a heterogeneous subcritical core configuration. Introducing thorium fuel into the core offers an effective way to transmute plutonium and minor actinide (MA and gain energy from this process. Transmutation rate as a function of burnup is estimated using MCNPX 2.7.0 code. Results show that by using the seed-blanket designed ADS, at 40 GWd/t burnup, 192 kg of plutonium and 156 kg of MA can be eliminated. Equivalently, 1  ADS can be able to transmute the transuranic (TRU waste from 2  LWRs. 14 units of ADS would be required to eliminate TRUs from the future reactors to be constructed in Vietnam.

  5. Accuracy Improvement of Neutron Nuclear Data on Minor Actinides

    Directory of Open Access Journals (Sweden)

    Harada Hideo

    2015-01-01

    Full Text Available Improvement of accuracy of neutron nuclear data for minor actinides (MAs and long-lived fission products (LLFPs is required for developing innovative nuclear system transmuting these nuclei. In order to meet the requirement, the project entitled as “Research and development for Accuracy Improvement of neutron nuclear data on Minor ACtinides (AIMAC” has been started as one of the “Innovative Nuclear Research and Development Program” in Japan at October 2013. The AIMAC project team is composed of researchers in four different fields: differential nuclear data measurement, integral nuclear data measurement, nuclear chemistry, and nuclear data evaluation. By integrating all of the forefront knowledge and techniques in these fields, the team aims at improving the accuracy of the data. The background and research plan of the AIMAC project are presented.

  6. Status of measurements of fission neutron spectra of Minor Actinides

    Energy Technology Data Exchange (ETDEWEB)

    Drapchinsky, L.; Shiryaev, B. [V.G. Khlopin Radium Inst., Saint Petersburg (Russian Federation)

    1997-03-01

    The report considers experimental and theoretical works on studying the energy spectra of prompt neutrons emitted in spontaneous fission and neutron induced fission of Minor Actinides. It is noted that neutron spectra investigations were done for only a small number of such nuclei, most measurements, except those of Cf-252, having been carried out long ago by obsolete methods and imperfectapparatus. The works have no detailed description of experiments, analysis of errors, detailed numerical information about results of experiments. A conclusion is made that the available data do not come up to modern requirements. It is necessary to make new measurements of fission prompt neutron spectra of transuranium nuclides important for the objectives of working out a conception of minor actinides transmutation by means of special reactors. (author)

  7. Recovery of minor actinides from irradiated superfact fuels

    Energy Technology Data Exchange (ETDEWEB)

    Apoltolidis, C.; Glatz, J.P.; Molinet, R.; Nicholl, A.; Pagliosa, G.; Romer, K.; Bokelund, H.; Koch, L. [European Commission, JRC, Institute fuer Transuranium Elements, Karlsruhe (Germany)

    1995-12-31

    It could be demonstrated that the reprocessing of fast reactor oxide fuels containing up to 45 % MA (Np and Am), irradiated in the PHENIX reactor in the frame of a transmutation study, is possible. The fuels were dissolved under PUREX type conditions in order to determine their behaviour in the head-end step of the reprocessing process. For one of the fuels containing 20 % Am and 20 % Np before irradiation, an almost complete partitioning of actinides from the dissolver solution could be achieved. Chromatographic extraction was used for the separation of the main bulk elements U, Pu and Np, whereas centrifugal extractors were used to separate the minor actinides from the remaining high level liquid wastes (HLLW). For the relevant radio-toxic isotopes a high recovery rate from the irradiation targets was reached. Those elements are thus available for new fuel fabrication. (authors) 12 refs.

  8. Status of measurements of fission neutron spectra of Minor Actinides

    Energy Technology Data Exchange (ETDEWEB)

    Drapchinsky, L.; Shiryaev, B. [V.G. Khlopin Radium Inst., Saint Petersburg (Russian Federation)

    1997-03-01

    The report considers experimental and theoretical works on studying the energy spectra of prompt neutrons emitted in spontaneous fission and neutron induced fission of Minor Actinides. It is noted that neutron spectra investigations were done for only a small number of such nuclei, most measurements, except those of Cf-252, having been carried out long ago by obsolete methods and imperfectapparatus. The works have no detailed description of experiments, analysis of errors, detailed numerical information about results of experiments. A conclusion is made that the available data do not come up to modern requirements. It is necessary to make new measurements of fission prompt neutron spectra of transuranium nuclides important for the objectives of working out a conception of minor actinides transmutation by means of special reactors. (author)

  9. Innovative SANEX process for trivalent actinides separation from PUREX raffinate

    Energy Technology Data Exchange (ETDEWEB)

    Sypula, Michal

    2013-07-01

    Recycling of nuclear spent fuel and reduction of its radiotoxicity by separation of long-lived radionuclides would definitely help to close the nuclear fuel cycle ensuring sustainability of the nuclear energy. Partitioning of the main radiotoxicity contributors followed by their conversion into short-lived radioisotopes is known as partitioning and transmutation strategy. To ensure efficient transmutation of the separated elements (minor actinides) the content of lanthanides in the irradiation targets has to be minimised. This objective can be attained by solvent extraction using highly selective ligands that are able to separate these two groups of elements from each other. The objective of this study was to develop a novel process allowing co-separation of minor actinides and lanthanides from a high active acidic feed solution with subsequent actinide recovery using just one cycle, so-called innovative SANEX process. The conditions of each step of the process were optimised to ensure high actinide separation efficiency. Additionally, screening tests of several novel lipophilic and hydrophilic ligands provided by University of Twente were performed. These tests were aiming in better understanding the influence of the extractant structural modifications onto An(III)/Ln(III) selectivity and complexation properties. Optimal conditions for minor actinides separation were found and a flow-sheet of a new innovative SANEX process was proposed. Tests using a single centrifugal contactor confirmed high Eu(III)/Am(III) separation factor of 15 while the lowest SF{sub Ln/Am} obtained was 6,5 (for neodymium). In addition, a new masking agent for zirconium was found as a substitution for oxalic acid. This new masking agent (CDTA) was also able to mask palladium without any negative influence on An(III)/Ln(III). Additional tests showed no influence of CDTA on plutonium present in the feed solution unlike oxalic acid which causes Pu precipitation. Therefore, CDTA was proposed as

  10. PREFACE: Actinides 2009

    Science.gov (United States)

    Rao, Linfeng; Tobin, James G.; Shuh, David K.

    2010-07-01

    This volume of IOP Conference Series: Materials Science and Engineering consists of 98 papers that were presented at Actinides 2009, the 8th International Conference on Actinide Science held on 12-17 July 2009 in San Francisco, California, USA. This conference was jointly organized by Lawrence Livermore National Laboratory and Lawrence Berkeley National Laboratory. The Actinides conference series started in Baden-Baden, Germany (1975) and this first conference was followed by meetings at Asilomar, CA, USA (1981), Aix-en-Provence, France (1985), Tashkent, USSR (1989), Santa Fe, NM, USA (1993), Baden-Baden, Germany (1997), Hayama, Japan (2001), and Manchester, UK (2005). The Actinides conference series provides a regular venue for the most recent research results on the chemistry, physics, and technology of the actinides and heaviest elements. Actinides 2009 provided a forum spanning a diverse range of scientific topics, including fundamental materials science, chemistry, physics, environmental science, and nuclear fuels. Of particular importance was a focus on the key roles that basic actinide chemistry and physics research play in advancing the worldwide renaissance of nuclear energy. Editors Linfeng Rao Lawrence Berkeley National Laboratory (lrao@lbl.gov) James G Tobin Lawrence Livermore National Laboratory (tobin1@llnl.gov) David K Shuh Lawrence Berkeley National Laboratory (dkshuh@lbl.gov)

  11. Principle and Uncertainty Quantification of an Experiment Designed to Infer Actinide Neutron Capture Cross-Sections

    Energy Technology Data Exchange (ETDEWEB)

    G. Youinou; G. Palmiotti; M. Salvatorre; G. Imel; R. Pardo; F. Kondev; M. Paul

    2010-01-01

    An integral reactor physics experiment devoted to infer higher actinide (Am, Cm, Bk, Cf) neutron cross sections will take place in the US. This report presents the principle of the planned experiment as well as a first exercise aiming at quantifying the uncertainties related to the inferred quantities. It has been funded in part by the DOE Office of Science in the framework of the Recovery Act and has been given the name MANTRA for Measurement of Actinides Neutron TRAnsmutation. The principle is to irradiate different pure actinide samples in a test reactor like INL’s Advanced Test Reactor, and, after a given time, determine the amount of the different transmutation products. The precise characterization of the nuclide densities before and after neutron irradiation allows the energy integrated neutron cross-sections to be inferred since the relation between the two are the well-known neutron-induced transmutation equations. This approach has been used in the past and the principal novelty of this experiment is that the atom densities of the different transmutation products will be determined with the Accelerator Mass Spectroscopy (AMS) facility located at ANL. While AMS facilities traditionally have been limited to the assay of low-to-medium atomic mass materials, i.e., A < 100, there has been recent progress in extending AMS to heavier isotopes – even to A > 200. The detection limit of AMS being orders of magnitude lower than that of standard mass spectroscopy techniques, more transmutation products could be measured and, potentially, more cross-sections could be inferred from the irradiation of a single sample. Furthermore, measurements will be carried out at the INL using more standard methods in order to have another set of totally uncorrelated information.

  12. Preliminary assessment of partitioning and transmutation as a radioactive waste management concept

    Energy Technology Data Exchange (ETDEWEB)

    Croff, A. G.; Tedder, D. W.; Drago, J. P.; Blomeke, J. O.; Perona, J. J.

    1977-09-01

    Partitioning (separating) the actinide elements from nuclear fuel cycle wastes and transmuting (burning) them to fission products in power reactors represents a potentially advanced concept of radioactive waste management which could reduce the long-term (greater than 1000 years) risk associated with geologic isolation of wastes. The greatest uncertainties lie in the chemical separations technology needed to recover greater than 99 percent of the actinides during the reprocessing of spent fuels and their refabrication as fresh fuels or target elements. Preliminary integrated flowsheets based on modifications of the Purex process and supplementary treatment by oxalate precipitation and ion exchange indicate that losses of plutonium in reprocessing wastes might be reduced from about 2.0 percent to 0.1 percent, uranium losses from about 1.7 percent to 0.1 percent, neptunium losses from 100 percent to about 1.2 percent, and americium and curium from 100 percent to about 0.5 percent. Mixed oxide fuel fabrication losses may be reduced from about 0.5 percent to 0.06 percent for plutonium and from 0.5 percent to 0.04 percent for uranium. Americium losses would be about 5.5 percent for the reference system. Transmutation of the partitioned actinides at a rate of 5 to 7 percent per year is feasible in both fast and thermal reactors, but additional studies are needed to determine the most suitable strategy for recycling them to reactors and to assess the major impacts of implementing the concept on fuel cycle operations and costs. It is recommended that the ongoing program to evaluate the feasibility, impacts, costs, and incentives of implementing partitioning-transmutation be continued until a firm assessment of its potentialities can be made. At the present level of effort, achievement of this objective should be possible by 1980. 27 tables, 50 figures.

  13. Chemistry of actinides; Chimie des actinides

    Energy Technology Data Exchange (ETDEWEB)

    Vitorge, P. [CEA/Saclay, Dept. d' Entreposage et de Stockage des Dechets (DESD), 91 - Gif-sur-Yvette (France)

    1999-07-01

    This article gives the basic data of the actinides chemistry, describes then qualitatively the main parts of the fuel cycle and concludes with quantitative data. The theoretical recalls give qualitative notions to explain the chemical reactivity of actinides and to understand thus the values of the thermodynamic data which allow quantitative anticipations at equilibrium. The Thermodynamic Data Base (TDB) of the NEA-OECD and the CEA in France have recently estimated some of them in using and developing methodologies whose some are presented here. Some current problems of actinides chemistry are described: analysis of the possibilities to (1)improve the reprocessing of long-lived actinides (2)anticipate their behaviour in the environment in order to compare the impact of the different options of the wastes management. The Pourbaix diagrams summarize the chemistry in solution; the author has added information on the solubility, the influence of the ionic strength and of the complexes formation in bicarbonate/carbonate (HCO{sub 3}{sup -}/CO{sub 3}{sup 2-}) media. The discussion on the choice of the equilibrium constants allows to point out the particular points, the dubiousness and the data which have to be proved. (O.M.)

  14. Optimization of moderated targets loading in LMFBR for minor actinides incineration

    Energy Technology Data Exchange (ETDEWEB)

    Wu Hongchun; Takeda, Toshikazu [Osaka Univ., Suita (Japan). Dept. of Nuclear Engineering

    1999-04-01

    Optimization of moderated targets loading in LMFBR for minor actinides (MAs) incineration has been performed in this paper. Results of many different composition ratios of moderated target mixture were compared. An optimum case was proposed which can offer good core performance and transmute MAs by about 73 percent (386 kg) and incinerate MAs by about 34 percent (181 kg) through 3 years of reactor operation. (author)

  15. Improved Actinide Neutron Capture Cross Sections Using Accelerator Mass Spectrometry

    Science.gov (United States)

    Bauder, W.; Pardo, R. C.; Kondev, F. G.; Kondrashev, S.; Nair, C.; Nusair, O.; Palchan, T.; Scott, R.; Seweryniak, D.; Vondrasek, R.; Collon, P.; Paul, M.; Youinou, G.; Salvatores, M.; Palmotti, G.; Berg, J.; Maddock, T.; Imel, G.

    2014-09-01

    The MANTRA (Measurement of Actinide Neutron TRAnsmutations) project will improve energy-integrated neutron capture cross section data across the actinide region. These data are incorporated into nuclear reactor models and are an important piece in understanding Generation IV reactor designs. We will infer the capture cross sections by measuring isotopic ratios from actinide samples, irradiated in the Advanced Test Reactor at INL, with Accelerator Mass Spectrometry (AMS) at ATLAS (ANL). The superior sensitivity of AMS allows us to extract multiple cross sections from a single sample. In order to analyze the large number of samples needed for MANTRA and to meet the goal of extracting multiple cross sections per sample, we have made a number of modifications to the AMS setup at ATLAS. In particular, we are developing a technique to inject solid material into the ECR with laser ablation. With laser ablation, we can better control material injection and potentially increase efficiency in the ECR, thus creating less contamination in the source and reducing cross talk. I will present work on the laser ablation system and preliminary results from our AMS measurements. The MANTRA (Measurement of Actinide Neutron TRAnsmutations) project will improve energy-integrated neutron capture cross section data across the actinide region. These data are incorporated into nuclear reactor models and are an important piece in understanding Generation IV reactor designs. We will infer the capture cross sections by measuring isotopic ratios from actinide samples, irradiated in the Advanced Test Reactor at INL, with Accelerator Mass Spectrometry (AMS) at ATLAS (ANL). The superior sensitivity of AMS allows us to extract multiple cross sections from a single sample. In order to analyze the large number of samples needed for MANTRA and to meet the goal of extracting multiple cross sections per sample, we have made a number of modifications to the AMS setup at ATLAS. In particular, we are

  16. Studies on the safety and transmutation behaviour of innovative fuels for light water reactors; Untersuchungen zum Sicherheits- und Transmutationsverhalten innovativer Brennstoffe fuer Leichtwasserreaktoren

    Energy Technology Data Exchange (ETDEWEB)

    Schitthelm, Oliver

    2012-07-01

    Nuclear power plants contribute a substantial part to the energy demand in industry. Today the most common fuel cycle uses enriched uranium which produces plutonium due to its {sup 238}U content. With respect to the long-term waste disposal Plutonium is an issue due to its heat production and radiotoxicity. This thesis consists of three main parts. In the first part the development and validation of a new code package MCBURN for spatial high resolution burnup simulations is presented. In the second part several innovative uranium-free and plutonium-burning fuels are evaluated on assembly level. Candidates for these fuels are a thorium/plutonium fuel and an inert matrix fuel consisting of plutonium dispersed in an enriched molybdenum matrix. The performance of these fuels is evaluated against existing MOX and enriched uranium fuels considering the safety and transmutation behaviour. The evaluation contains the boron efficiency, the void coefficient, the doppler coefficient and the net balances of every radionuclide. In the third part these innovative fuels are introduced into a German KONVOI reactor core. Considering todays approved usage of MOX fuels a partial loading of one third of innovative fuels and two third of classical uranium fuels was analysed. The efficiency of the plutonium depletion is determined by the ratio of the production of higher isotopes compared to the plutonium depletion. Todays MOX-fuels transmutate about 25% to 30% into higher actinides as Americium or Curium. In uranium-free fuels this ratio is about 10% due to the lack of additional plutonium production. The analyses of the reactor core have shown that one third of MOX fuel is not capable of a net reduction of plutonium. On the other hand a partial loading with thorium/plutonium fuel incinerates about half the amount of plutonium produced by an uranium only core. If IMF is used the ratio increases to about 75%. Considering the safety behavior all fuels have shown comparable results.

  17. Neutron transmutation doped silicon detectors

    Energy Technology Data Exchange (ETDEWEB)

    Kim, K.; Krejner, Kh.; Ito, D.; Khusimi, K.; Okava, S.; Sirejsi, F.

    1984-01-01

    A method of doping neutron transmutation during (NTD) of Si crystals is described. Characteristics of detectors made of crystals obtained by the NTD method at low and room temperatures are measured. The possibility is studied of using the NTD method to produce Si crystals with a longer lifetime of non-base charge carriers, high specific resistance and more even distribution of specific resistance over the detector radius. The NTD method is based on /sup 30/Si isotope transmutation into /sup 31/Si following the (n, ..gamma..)-reaction. The /sup 31/Si isotope is unstable and transforms to /sup 31/P while emitting ..beta../sup -/. The NTD method consists in introduction of purified gaseous monosilan SiH/sub 4/ into the furnace to undergo thermal decomposition at 860 deg C with the formation of polycrystalline n-type Si. The polycrystalline Si prepared is treated mechanically and, after purification by the method of a ''floating zone'' in vacuum and in argon irradiated by a thermal neutron flux with the a density of 5x10/sup 11/ neUtr/(cm/sup 2/ x s) for 30-75 min. An analysis of the data obtained shows that the specifications of the Si detectors prepared by the NTD method are the same as those of conventional Si-detectors widely used nowadays but their cost of production is considerably lower.

  18. Detailed study of transmutation scenarios involving present day reactor technologies; Etude detaillee des scenarios de transmutation faisant appel aux technologies actuelles pour les reacteurs

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2003-07-01

    This document makes a detailed technical evaluation of three families of separation-transmutation scenarios for the management of radioactive wastes. These scenarios are based on 2 parks of reactors which recycle plutonium and minor actinides in an homogeneous way. A first scenario considers the multi-recycling of Pu and Np and the mono-recycling of Am and Cm using both PWRs and FBRs. A second scenario is based on PWRs only, while a third one considers FBRs only. The mixed PWR+FBR scenario requires innovative options and gathers more technical difficulties due to the americium and curium management in a minimum flux of materials. A particular attention has been given to the different steps of the fuel cycle (fuels and targets fabrication, burnup, spent fuel processing, targets management). The feasibility of scenarios of homogeneous actinides recycling in PWRs-only and in FBRs-only has been evaluated according to the results of the first scenario: fluxes of materials, spent fuel reprocessing by advanced separation, impact of the presence of actinides on PWRs and FBRs operation. The efficiency of the different scenarios on the abatement of wastes radio-toxicity is presented in conclusion. (J.S.)

  19. Transmutation doping of silicon solar cells

    Science.gov (United States)

    Wood, R. F.; Westbrook, R. D.; Young, R. T.; Cleland, J. W.

    1977-01-01

    Normal isotopic silicon contains 3.05% of Si-30 which transmutes to P-31 after thermal neutron absorption, with a half-life of 2.6 hours. This reaction is used to introduce extremely uniform concentrations of phosphorus into silicon, thus eliminating the areal and spatial inhomogeneities characteristic of chemical doping. Annealing of the lattice damage in the irradiated silicon does not alter the uniformity of dopant distribution. Transmutation doping also makes it possible to introduce phosphorus into polycrystalline silicon without segregation of the dopant at the grain boundaries. The use of neutron transmutation doped (NTD) silicon in solar cell research and development is discussed.

  20. Partitioning and transmutation. Annual Report 1997

    Energy Technology Data Exchange (ETDEWEB)

    Enarsson, Aa.; Landgren, A.; Liljenzin, J.O.; Skaalberg, M.; Spjuth, L. [Chalmers Univ. of Technology, Goeteborg (Sweden). Dept. of Nuclear Chemistry

    1997-12-01

    The current research project on partitioning and transmutation at the Dept. of Nuclear Chemistry, CTH, has the primary objective to investigate separation processes useful in connection with transmutation of long-lived radionuclides in high level nuclear waste. Partitioning is necessary in order to recover and purify the elements before and after each irradiation in a P and T treatment. In order to achieve a high transmutation efficiency the chemical separation process used must have small losses to various waste streams. At present, only aqueous based separation processes are known to be able to achieve the high recovery and separation efficiencies necessary for a useful P and T process. Refs, figs, tabs.

  1. The ALMR actinide burning system

    Energy Technology Data Exchange (ETDEWEB)

    Quinn, J.E. (General Electric Co., San Jose, CA (United States))

    1993-01-01

    The advanced liquid-metal reactor (ALMR) actinide burning system is being developed under the sponsorship of the US Department of Energy to bring its unique capabilities to fruition for deployment in the early 21st century. The system consists of four major parts: the reactor plant, the metal fuel and its recycle, the processing of light water reactor (LWR) spent fuel to extract the actinides, and the development of a residual waste package. This paper addresses the status and outlook for each of these four major elements. The ALMR is being developed by an industrial group under the leadership of General Electric (GE) in a cost-sharing arrangement with the US Department of Energy. This effort is nearing completion of the advanced conceptual design phase and will enter the preliminary design phase in 1994. The innovative modular reactor design stresses simplicity, economics, reliability, and availability. The design has evolved from GE's PRISM design initiative and has progressed to the final stages of a prelicensing review by the US Nuclear Regulatory Commission (NRC); a safety evaluation report is expected by the end of 1993. All the major issues identified during this review process have been technically resolved. The next design phases will focus on implementation of the basic safety philosophy of passive shutdown to a safe, stable condition, even without scram, and passive decay heat removal. Economic projections to date show that it will be competitive with non- nuclear and advanced LWR nuclear alternatives.

  2. Apparatus for nuclear transmutation and power production using an intense accelerator-generated thermal neutron flux

    Science.gov (United States)

    Bowman, Charles D.

    1992-01-01

    Apparatus for nuclear transmutation and power production using an intense accelerator-generated thermal neutron flux. High thermal neutron fluxes generated from the action of a high power proton accelerator on a spallation target allows the efficient burn-up of higher actinide nuclear waste by a two-step process. Additionally, rapid burn-up of fission product waste for nuclides having small thermal neutron cross sections, and the practicality of small material inventories while achieving significant throughput derive from employment of such high fluxes. Several nuclear technology problems are addressed including 1. nuclear energy production without a waste stream requiring storage on a geological timescale, 2. the burn-up of defense and commercial nuclear waste, and 3. the production of defense nuclear material. The apparatus includes an accelerator, a target for neutron production surrounded by a blanket region for transmutation, a turbine for electric power production, and a chemical processing facility. In all applications, the accelerator power may be generated internally from fission and the waste produced thereby is transmuted internally so that waste management might not be required beyond the human lifespan.

  3. Safe management of actinides in the nuclear fuel cycle: Role of mineralogy; La gestion des actinides dans le cycle du combustible nucleaire: le role de la mineralogie

    Energy Technology Data Exchange (ETDEWEB)

    Ewing, R.C. [Department of Nuclear Engineering and Radiological Sciences, Department of Geological Sciences, Department of Materials Science and Engineering, University of Michigan, Ann Arbor, Michigan 48109-1005 (United States)

    2011-02-15

    During the past 60 years, more than 1800 metric tonnes of Pu, and substantial quantities of the 'minor' actinides, such as Np, Am and Cm, have been generated in nuclear reactors. Some of these transuranium elements can be a source of energy in fission reactions (e.g., {sup 239}Pu), a source of fissile material for nuclear weapons (e.g., {sup 239}Pu and {sup 237}Np), and of environmental concern because of their long-half lives and radiotoxicity (e.g., {sup 239}Pu and {sup 237}Np). There are two basic strategies for the disposition of these heavy elements: (1) to 'burn' or transmute the actinides using nuclear reactors or accelerators; (2) to 'sequester' the actinides in chemically durable, radiation-resistant materials that are suitable for geologic disposal. There has been substantial interest in the use of actinide-bearing minerals, especially isometric pyrochlore, A{sub 2}B{sub 2}O{sub 7} (A rare earths; B = Ti, Zr, Sn, Hf), for the immobilization of actinides, particularly plutonium, both as inert matrix fuels and nuclear waste forms. Systematic studies of rare-earth pyrochlores have led to the discovery that certain compositions (B = Zr, Hf) are stable to very high doses of alpha-decay event damage. Recent developments in our understanding of the properties of heavy element solids have opened up new possibilities for the design of advanced nuclear fuels and waste forms. (author)

  4. Transmutation: The Roots of the Dream.

    Science.gov (United States)

    Karpenko, Vladimir

    1995-01-01

    Examines the history of alchemical attempts at transmutation and classifies them by differing approaches and techniques. Traces the development of alchemy in Asia, Europe, and the Middle East, and compares alchemy with craftsmanship. (18 references) (DDR)

  5. Reduction of minor actinides for recycling in a light water reactor; Reduccion de actinidos menores por reciclado en un reactor de agua ligera

    Energy Technology Data Exchange (ETDEWEB)

    Martinez C, E.; Ramirez S, J. R.; Alonso V, G., E-mail: eduardo.martinez@inin.gob.mx [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

    2015-09-15

    The aim of actinide transmutation from spent nuclear fuel is the reduction in mass of high-level waste which must be stored in geological repositories and the lifetime of high-level waste; these two achievements will reduce the number of repositories needed, as well as the duration of storage. The present work is directed towards the evaluation of an advanced nuclear fuel cycle in which the minor actinides (Np, Am and Cm) could be recycled to remove most of the radioactive material; a reference of actinides production in standard nuclear fuel of uranium at the end of its burning in a BWR is first established, after a design of fuel rod containing 6% of minor actinides in a matrix of uranium from the enrichment lines is proposed, then 4 fuel rods of standard uranium are replaced by 4 actinides bars to evaluate the production and transmutation of them and finally the minor actinides reduction in the fuel is evaluated. In the development of this work the calculation tool are the codes: Intrepin-3, Casmo-4 and Simulate-3. (Author)

  6. Device for Detecting Actinides, Method for Detecting Actinides

    Energy Technology Data Exchange (ETDEWEB)

    Stevens, Fred J.; Wilkins-Stevens, Priscilla

    1998-10-29

    A heavy metal detector is provided comprising a first molecule and a second molecule, whereby the first and second molecules interact in a predetermined manner; a first region on the first molecule adapted to interact with an actinide; and a second region on the second molecule adapted to interact with the actinide, whereby the interactions of the actinide with the regions effect the predetermined manner of interaction between the molecules.

  7. Lanthanides and actinides extraction by calixarenes containing CMPO groups; Extraction des lanthanides et des actinides au moyen de calixarenes portant des groupements CMPO

    Energy Technology Data Exchange (ETDEWEB)

    Garcia Carrera, A

    2001-07-01

    In the framework of the French program SPIN concerning the radioactive waste management, researches are performed to develop processes allowing the separation of long-lived radioisotopes in order to their transmutation or their specific conditioning. These studies deal with the extraction and the separation of trivalent lanthanides and actinides in acid solution. Many systems ''calixarene-diluent-aqueous phase'' are examined by extraction liquid-liquid and membrane transport. The extraction efficiency and the selectivity of the synthesized calixarene-CMPO and of the CMPO are compared with these cations, as the nitric acid extraction by these molecules. (A.L.B.)

  8. The impact of the core configuration on safety and transmutation behavior in an accelerator driven system; Auswirkung der Brennstoffwahl auf das Transmutationsverhalten in einem beschleunigergetriebenen System

    Energy Technology Data Exchange (ETDEWEB)

    Biss, K.; Nabbi, R.; Thomauske, B. [RWTH Aachen Univ. (Germany). Inst. fuer Nuklearen Brennstoffkreislauf (INBK)

    2012-11-01

    For the reduction of the long-term hazards of high-level wastes transmutation is one of the candidate techniques. For an effective conversion of transuranic elements, esp. minor actinides, the use of accelerator driven systems (ADS) is the favored concept. The subcritical system AGATE (advanced gas-cooled accelerator driven transmutation experiment)is a 100 MW(th) facility using a proton beam to produce the required spallation neutrons. The fuel zone includes 120 uniform fuel elements with hexagonal structure (each one with 91 fuel rods) in an annular configuration around the spallation target. Neutron flux and energy spectra are determined and averaged for each zone allowing a fast calculation of fuel element variants and geometry variations. For modeling the Monte Carlo code MCNPX 2.7 is used. The transmutation rate for pure PuMA fuel show high values for americium, but the isotope analysis shows that the largest fraction is transmuted to plutonium. The use of thorium as matrix material reduces the transmutation rate of transuranic elements but allows a long-term burnup cycle without required fuel element replacement.

  9. Validation of minor actinides fission neutron cross-sections

    Directory of Open Access Journals (Sweden)

    Pešić Milan P.

    2015-01-01

    Full Text Available Verification of neutron fission cross-sections of minor actinides from some recently available evaluated nuclear data libraries was carried out by comparison of the reaction rates calculated by the MCNP6.1 computer code to the experimental values. The experimental samples, containing thin layers of 235U, 237Np, 238,239,240,241Pu, 242mAm, 243Cm, 245Cm, and 247Cm, deposited on metal support and foils of 235U (pseudo-alloy 27Al + 235U, 238U, natIn, 64Zn, 27Al, and multi-component sample alloy 27Al + 55Mn + natCu + natLu + 197Au, were irradiated in the channels of the tank containing fluorine salts 0.52NaF + 0.48ZrF4, labelled as the Micromodel Salt Blanket, inserted in the lattice centre of the MAKET heavy water critical assembly at the Institute for Theoretical and Experimental Physics, Moscow. This paper is a continuation of earlier initiated scientific-research activities carried out for validation of the evaluated fission cross-sections of actinides that were supposed to be used for the quality examination of the fuel design of the accelerator driven systems or fast reactors, and consequently, determination of transmutation rates of actinides, and therefore, determination of operation parameters of these reactor facilities. These scientific-research activities were carried out within a frame of scientific projects supported by the International Science and Technology Center and the International Atomic Energy Agency co-ordinated research activities, from 1999 to 2010. Obtained results confirm that further research is needed in evaluations in order to establish better neutron cross-section data for the minor actinides and selected nuclides which could be used in the accelerator driven systems or fast reactors.

  10. Safe management of actinides in the nuclear fuel cycle: Role of mineralogy

    Science.gov (United States)

    Ewing, Rodney C.

    2011-02-01

    During the past 60 years, more than 1800 metric tonnes of Pu, and substantial quantities of the "minor" actinides, such as Np, Am and Cm, have been generated in nuclear reactors. Some of these transuranium elements can be a source of energy in fission reactions (e.g., 239Pu), a source of fissile material for nuclear weapons (e.g., 239Pu and 237Np), and of environmental concern because of their long-half lives and radiotoxicity (e.g., 239Pu and 237Np). There are two basic strategies for the disposition of these heavy elements: (1) to "burn" or transmute the actinides using nuclear reactors or accelerators; (2) to "sequester" the actinides in chemically durable, radiation-resistant materials that are suitable for geologic disposal. There has been substantial interest in the use of actinide-bearing minerals, especially isometric pyrochlore, A 2B 2O 7 (A = rare earths; B = Ti, Zr, Sn, Hf), for the immobilization of actinides, particularly plutonium, both as inert matrix fuels and nuclear waste forms. Systematic studies of rare-earth pyrochlores have led to the discovery that certain compositions (B = Zr, Hf) are stable to very high doses of alpha-decay event damage. Recent developments in our understanding of the properties of heavy element solids have opened up new possibilities for the design of advanced nuclear fuels and waste forms.

  11. Partitioning and transmutation. Current developments - 2007. A report from the Swedish reference group on P-T-research

    Energy Technology Data Exchange (ETDEWEB)

    Ahlstroem, Per-Eric (ed.) [Swedish Nuclear Fuel and Waste Management Co., Stockholm (Sweden); Blomgren, Jan [Uppsala Univ. (Sweden). Dept. of Neutron Research; Ekberg, Christian; Englund, Sofie; Fermvik, Anna; Liljenzin, Jan-Olov; Retegan, Teodora; Skarnemark, Gunnar [Chalmers Univ. of Technology, Goeteborg (Sweden); Eriksson, Marcus; Seltborg, Per; Wallenius, Jan; Westlen, Daniel [Royal Inst. of Technology, Stockholm (Sweden)

    2007-06-15

    This report is written on behalf of the Swedish reference group for research on partitioning and transmutation. The reference group has been assembled by SKB and its members represent the teams that are active in this field at Swedish universities. The present report summarises the progress in the field through the years 2004-2006. A prerequisite for transmutation by irradiation with neutrons is that the nuclides to be transmuted are separated (partitioned) from the other nuclides in the spent fuel. In particular the remaining uranium must be taken away unless you want to produce more plutonium and other transuranium elements. Separation of the various elements can at least in principle be achieved by mechanical and chemical processes. Currently there exist some large scale facilities for separation of uranium and plutonium from the spent fuel-reprocessing plants. These can, however, not separate the minor actinides - neptunium, americium and curium - from the high level waste that goes to a repository. Plutonium constitutes about 90% of the transuranium elements in fuel from light water reactors. The objective of current research on partitioning is to find and develop processes suitable for separation of the heavier actinides (and possibly some long-lived fission products) on an industrial scale. The objective of current research on transmutation is to define, investigate and develop facilities that may be suitable for transmutation of the aforementioned long-lived radionuclides. The research on partitioning has made important progress in recent years. In some cases one has succeeded to separate americium and curium. Many challenges remain however. Within hydrochemistry one has achieved sufficiently good distribution and separation factors. The focus turns now towards development of an operating process. The search for ligands that give sufficiently good extraction and separation will continue but with less intensity. The emphasis will rather be on improving

  12. Transmutation Theory in the Greek Alchemical Corpus.

    Science.gov (United States)

    Dufault, Olivier

    2015-08-01

    This paper studies transmutation theory as found in the texts attributed to Zosimus of Panopolis, "the philosopher Synesius," and "the philosopher Olympiodorus of Alexandria." It shows that transmutation theory (i.e. a theory explaining the complete transformation of substances) is mostly absent from the work attributed to these three authors. The text attributed to Synesius describes a gilding process, which is similar to those described by Pliny and Vitruvius. The commentary attributed to Olympiodorus is the only text studied here that describes something similar to a transmutation theory. It is unclear, however, if this was a theory of transmutation or if the writer meant something more like the literal meaning of the word "ekstrophē," a term used to describe the transformation of metals, as the "turning inside-out" of what is hidden in a substance. A similar conception of ekstrophē can be found in the works of Zosimus, who discussed transmutation to make an analogy with self-purification processes, which, from the perspective of his own anthropogony, consisted in the "turning inside-out" of the "inner human" (esō anthrōpos).

  13. Partitioning and transmutation. Annual Report 1999

    Energy Technology Data Exchange (ETDEWEB)

    Ekberg, C.; Enarsson, Aa.; Gustavsson, C.; Landgren, A.; Liljenzin, J.O.; Spjuth, L. [Chalmers Univ. of Technology, Goeteborg (Sweden). Dept. of Nuclear Chemistry

    2000-05-01

    The current research project on partitioning and transmutation at the Dept. of Nuclear Chemistry, CTH, has the primary objective to investigate separation processes useful in connection with transmutation of long-lived radionuclides in high level nuclear waste. Partitioning is necessary in order to recover and purify the elements before and after each irradiation in a P and T treatment. In order to achieve a high transmutation efficiency the chemical separation process used must have small losses to various waste streams. At present, only aqueous based separation processes are known to be able to achieve the high recovery and separation efficiencies necessary for a useful P and T process. During 1999 two of the three PhD students in this project have finalised their dissertations. Lena Spjuth has been working with oligo pyridines, triazines and malonamides; Anders Landgren has studied Aliquat-336 and redox kinetics. Two papers, included as appendices in the report, have been separately indexed.

  14. The Transmuted Generalized Inverse Weibull Distribution

    Directory of Open Access Journals (Sweden)

    Faton Merovci

    2014-05-01

    Full Text Available A generalization of the generalized inverse Weibull distribution the so-called transmuted generalized inverse Weibull distribution is proposed and studied. We will use the quadratic rank transmutation map (QRTM in order to generate a flexible family of probability distributions taking the generalized inverseWeibull distribution as the base value distribution by introducing a new parameter that would offer more distributional flexibility. Various structural properties including explicit expressions for the moments, quantiles, and moment generating function of the new distribution are derived. We propose the method of maximum likelihood for estimating the model parameters and obtain the observed information matrix. A real data set are used to compare the flexibility of the transmuted version versus the generalized inverse Weibull distribution.

  15. ENHANCING ADVANCED CANDU PROLIFERATION RESISTANCE FUEL WITH MINOR ACTINIDES

    Energy Technology Data Exchange (ETDEWEB)

    Gray S. Chang

    2010-05-01

    The advanced nuclear system will significantly advance the science and technology of nuclear energy systems and to enhance the spent fuel proliferation resistance. Minor actinides (MA) are viewed more as a resource to be recycled, and transmuted to less hazardous and possibly more useful forms, rather than simply disposed of as a waste stream in an expensive repository facility. MAs can play a much larger part in the design of advanced systems and fuel cycles, not only as additional sources of useful energy, but also as direct contributors to the reactivity control of the systems into which they are incorporated. In this work, an Advanced CANDU Reactor (ACR) fuel unit lattice cell model with 43 UO2 fuel rods will be used to investigate the effectiveness of a Minor Actinide Reduction Approach (MARA) for enhancing proliferation resistance and improving the fuel cycle performance. The main MARA objective is to increase the 238Pu / Pu isotope ratio by using the transuranic nuclides (237Np and 241Am) in the high burnup fuel and thereby increase the proliferation resistance even for a very low fuel burnup. As a result, MARA is a very effective approach to enhance the proliferation resistance for the on power refueling ACR system nuclear fuel. The MA transmutation characteristics at different MA loadings were compared and their impact on neutronics criticality assessed. The concept of MARA, significantly increases the 238Pu/Pu ratio for proliferation resistance, as well as serves as a burnable absorber to hold-down the initial excess reactivity. It is believed that MARA can play an important role in atoms for peace and the intermediate term of nuclear energy reconnaissance.

  16. Transmuted New Generalized Inverse Weibull Distribution

    Directory of Open Access Journals (Sweden)

    Muhammad Shuaib Khan

    2017-06-01

    Full Text Available This paper introduces the transmuted new generalized inverse Weibull distribution by using the quadratic rank transmutation map (QRTM scheme studied by Shaw et al. (2007. The proposed model contains the twenty three lifetime distributions as special sub-models. Some mathematical properties of the new distribution are formulated, such as quantile function, Rényi entropy, mean deviations, moments, moment generating function and order statistics. The method of maximum likelihood is used for estimating the model parameters. We illustrate the flexibility and potential usefulness of the new distribution by using reliability data.

  17. Heterogeneous Transmutation Sodium Fast Reactor

    Energy Technology Data Exchange (ETDEWEB)

    S. E. Bays

    2007-09-01

    The threshold-fission (fertile) nature of Am-241 is used to destroy this minor actinide by capitalizing upon neutron capture instead of fission within a sodium fast reactor. This neutron-capture and its subsequent decay chain leads to the breeding of even neutron number plutonium isotopes. A slightly moderated target design is proposed for breeding plutonium in an axial blanket located above the active “fast reactor” driver fuel region. A parametric study on the core height and fuel pin diameter-to-pitch ratio is used to explore the reactor and fuel cycle aspects of this design. This study resulted in both non-flattened and flattened core geometries. Both of these designs demonstrated a high capacity for removing americium from the fuel cycle. A reactivity coefficient analysis revealed that this heterogeneous design will have comparable safety aspects to a homogeneous reactor of comparable size. A mass balance analysis revealed that the heterogeneous design may reduce the number of fast reactors needed to close the current once-through light water reactor fuel cycle.

  18. System and safety studies of accelerator driven transmutation. Annual Report 2003

    Energy Technology Data Exchange (ETDEWEB)

    Gudowski, Waclaw; Wallenius, Jan; Tucek, Kamil [Royal Inst. of Technology, Stockholm (Sweden). Dept. of Nuclear and Reactor Physics] [and others

    2004-12-01

    The research on safety of Accelerator-Driven Transmutation Systems (ADS) at the Dept. of Nuclear and Reactor Physics reported here has been focused on different aspects of safety of the Accelerator-Driven Transmutation Systems and on Transmutation research in more general terms. An overview of the topics of our research is given in the Summary which is followed by detailed reports as separate chapters or subchapters. Some of the research topics reported in this report are referred to appendices, which have been published in the open literature. Topics, which are not yet published, are described with more details in the main part of this report. Main focus has been, as before, largely determined by the programme of the European projects of the 5th Framework Programme in which KTH is actively participating. In particular: a) ADS core design and development of advanced nuclear fuel optimised for high transmutation rates and good safety features. This activity includes even computer modeling of nuclear fuel production. Three different ADS-core concept are being investigated: Conceptual design of Pb-Bi cooled core with nitride fuel so called Sing-Sing Core developed at KTH; Pb-Bi cooled core with oxide fuel so called ANSALDO design for the European Project PDS-XADS; Gas cooled core with oxide fuel a design investigated for the European Project PDS-XADS. b) analysis of potential of advance fuels, in particular nitrides with high content of minor actinides; c) analysis of ADS-dynamics and assessment of major reactivity feedbacks; d) emergency heat removal from ADS; e) participation in ADS: MUSE (CEA-Cadarache), YALINA subcritical experiment in Minsk and designing of the subcritical experiment SAD in Dubna; f) theoretical and simulation studies of radiation damage in high neutron (and/or proton) fluxes; g) computer code and nuclear data development relevant for simulation and optimization of ADS, validation of the MCB code and sensitivity analysis; h) studies of

  19. AECL/U.S. INERI - Development of Inert Matrix Fuels for Plutonium and Minor Actinide Management in Power Reactors Fuel Requirements and Down-Select Report

    Energy Technology Data Exchange (ETDEWEB)

    William Carmack; Randy Fielding; Pavel Medvedev; Mitch Meyer

    2005-08-01

    This report documents the first milestone of the International Nuclear Energy Research Initiative (INERI) U.S./Euratom Joint Proposal 1.8 entitled “Development of Inert Matrix Fuels for Plutonium and Minor Actinide Management in Light-Water Reactors.” The milestone represents the assessment and preliminary study of a variety of fuels that hold promise as transmutation and minor actinide burning fuel compositions for light-water reactors. The most promising fuels of interest to the participants on this INERI program have been selected for further study. These fuel compositions are discussed in this report.

  20. Characterization of lead-bismuth eutectic target material for accelerator driven transmuters

    Energy Technology Data Exchange (ETDEWEB)

    Gohar, Yousry E-mail: gohar@anl.gov

    2003-05-15

    Lead-bismuth eutectic (LBE) is under consideration as a target material with high-energy protons for generating neutrons to drive actinide and fission product transmuters. A characterization has been performed to study the performance of this target material as a function of the main variables and the design selections. The characterization includes the neutron yield, the spatial energy deposition, the neutron spectrum, the beam window performance, and the target buffer requirements. The characterization has also considered high-energy deuteron particles to study the impact on the target neutronic performance. The obtained results quantify the LBE target material performance with proton or deuteron particles as a function of the target variables and selections.

  1. SPECIFIC SEQUESTERING AGENTS FOR THE ACTINIDES

    Energy Technology Data Exchange (ETDEWEB)

    Raymond, Kenneth N.; Smith, William L.; Weitl, Frederick L.; Durbin, Patricia W.; Jones, E.Sarah; Abu-Dari, Kamal; Sofen, Stephen R.; Cooper, Stephen R.

    1979-09-01

    This paper summarizes the current status of a continuing project directed toward the synthesis and characterization of chelating agents which are specific for actinide ions - especially Pu(IV) - using a biomimetic approach that relies on the observation that Pu(IV) and Fe(III) has marked similarities that include their biological transport and distribution in mammals. Since the naturally-occurring Fe(III) sequestering agents produced by microbes commonly contain hydroxamate and catecholate functional groups, these groups should complex the actinides very strongly and macrocyclic ligands incorporating these moieties are being prepared. We have reported the isolation and structure analysis of an isostructural series of tetrakis(catecholato) complexes with the general stoichiometry Na{sub 4}[M(C{sub 6}H{sub 4}O{sub 2}){sub 4}] • 21 H{sub 2}O (M = Th, U, Ce, Hf). These complexes are structural archetypes for the cavity that must be formed if an actinide-specific sequestering agent is to conform ideally to the coordination requirements of the central metal ion. The [M(cat){sub 4}]{sup 4-} complexes have the D{sub 2d} symmetry of the trigonal-faced dodecahedron.. The complexes Th [R'C(0)N(O)R]{sub 4} have been prepared where R = isopropyl and R' = t-butyl or neopentyl. The neopentyl derivative is also relatively close to an idealized D{sub 2d} dodecahedron, while the sterically more hindered t-butyl compound is distorted toward a cubic geometry. The synthesis of a series of 2, 3-dihydroxy-benzoyl amide derivatives of linear and cyclic tetraaza- and diazaalkanes is reported. Sulfonation of these compounds improves the metal complexation and in vivo removal of plutonium from test animals. These results substantially exceed the capabilities of compounds presently used for the therapeutic treatment of actinide contamination.

  2. Neutron transmutation doping of silicon by magnesium

    Energy Technology Data Exchange (ETDEWEB)

    Sobolev, N.A.; Shek, E.I. (A.F. Ioffe Physico-Technical Inst., Saint Petersburg (Russian Federation)); Shabalin, E.P. (Joint Inst. for Nuclear Research, Dubna (Russian Federation). Lab. of Neutron Physics)

    1993-11-01

    We have demonstrated that irradiation of silicon by fast neutrons and subsequent annealing lead to doping due to formation of Mg-related centers. The impurity introduction rates were calculated as a result of transmutation reactions during irradiation in the IBR-30 reactor. The behaviour of the resistivity of irradiated samples during annealing was studied. (author).

  3. Transmutation Fuels Campaign FY-09 Accomplishments Report

    Energy Technology Data Exchange (ETDEWEB)

    Lori Braase

    2009-09-01

    This report summarizes the fiscal year 2009 (FY-08) accomplishments for the Transmutation Fuels Campaign (TFC). The emphasis is on the accomplishments and relevance of the work. Detailed description of the methods used to achieve the highlighted results and the associated support tasks are not included in this report.

  4. Build-up of actinides in irradiated fuel rods of the ET-RR-1 reactor

    Energy Technology Data Exchange (ETDEWEB)

    Adib, M.; Naguib, K.; Morcos, H.N

    2001-09-01

    The content concentrations of actinides are calculated as a function of operating reactor regime and cooling time at different percentage of fuel burn-up. The build-up transmutation equations of actinides content in an irradiated fuel are solved numerically .A computer code BAC was written to operate on a PC computer to provide the required calculations. The fuel element of 10% {sup 235}U enrichment of ET-RR-1 reactor was taken as an example for calculations using the BAC code. The results are compared with other calculations for the ET-RR-1 fuel rod. An estimation of fissile build-up content of a proposed new fuel of 20% {sup 235}U enrichment for ET-RR-1 reactor is given. The sensitivity coefficients of build-up plutonium concentrations as a function of cross-section data uncertainties are also calculated.

  5. The EBR-II X501 Minor Actinide Burning Experiment

    Energy Technology Data Exchange (ETDEWEB)

    W. J. Carmack; M. K. Meyer; S. L. Hayes; H. Tsai

    2008-01-01

    The X501 experiment was conducted in EBR II as part of the Integral Fast Reactor program to demonstrate minor actinide burning through the use of a homogeneous recycle scheme. The X501 subassembly contained two metallic fuel elements loaded with relatively small quantities of americium and neptunium. Interest in the behavior of minor actinides (MA) during fuel irradiation has prompted further examination of existing X501 data and generation of new data where needed in support of the U.S. waste transmutation effort. The X501 experiment is one of the few MA bearing fuel irradiation tests conducted worldwide, and knowledge can be gained by understanding the changes in fuel behavior due to addition of MAs. Of primary interest are the effect of the MAs on fuel cladding chemical interaction and the redistribution behavior of americium. The quantity of helium gas release from the fuel and any effects of helium on fuel performance are also of interest. It must be stressed that information presented at this time is based on the limited PIE conducted in 1995–1996 and, currently, represents a set of observations rather than a complete understanding of fuel behavior. This report provides a summary of the X501 fabrication, characterization, irradiation, and post irradiation examination.

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

    Science.gov (United States)

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

    2015-04-01

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

  7. Actinides in irradiated graphite of RBMK-1500 reactor

    Energy Technology Data Exchange (ETDEWEB)

    Plukienė, R., E-mail: rita@ar.fi.lt; Plukis, A.; Barkauskas, V.; Gudelis, A.; Gvozdaitė, R.; Duškesas, G.; Remeikis, V.

    2014-10-01

    Highlights: • Activation of actinides in the graphite of the RBMK-1500 reactor was analyzed. • Numerical modeling using SCALE 6.1 and MCNPX was used for actinide calculation. • Measurements of the irradiated graphite sample were used for model validation. • Results are important for further decommissioning process of the RBMK type reactors. - Abstract: The activation of graphite in the nuclear power plants is the problem of high importance related with later graphite reprocessing or disposal. The activation of actinide impurities in graphite due to their toxicity determines a particular long term risk to waste management. In this work the activation of actinides in the graphite constructions of the RBMK-1500 reactor is determined by nuclear spectrometry measurements of the irradiated graphite sample from the Ignalina NPP Unit I and by means of numerical modeling using two independent codes SCALE 6.1 (using TRITON-VI sequence) and MCNPX (v2.7 with CINDER). Both models take into account the 3D RBMK-1500 reactor core fragment with explicit graphite construction including a stack and a sleeve but with a different simplification level concerning surrounding graphite and construction of control roads. The verification of the model has been performed by comparing calculated and measured isotope ratios of actinides. Also good prediction capabilities of the actinide activation in the irradiated graphite have been found for both calculation approaches. The initial U impurity concentration in the graphite model has been adjusted taking into account the experimental results. The specific activities of actinides in the irradiated RBMK-1500 graphite constructions have been obtained and differences between numerical simulation results, different structural parts (sleeve and stack) as well as comparison with previous results (Ancius et al., 2005) have been discussed. The obtained results are important for further decommissioning process of the Ignalina NPP and other RBMK

  8. Prognosis and comparison of performances of composite CERCER and CERMET fuels dedicated to transmutation of TRU in an EFIT ADS

    Science.gov (United States)

    Sobolev, V.; Uyttenhove, W.; Thetford, R.; Maschek, W.

    2011-07-01

    The neutronic and thermomechanical performances of two composite fuel systems: CERCER with (Pu,Np,Am,Cm)O 2-x fuel particles in ceramic MgO matrix and CERMET with metallic Mo matrix, selected for transmutation of minor actinides in the European Facility for Industrial Transmutation (EFIT), were analysed aiming at their optimisation. The ALEPH burnup code system, based on MNCPX and ORIGEN codes and JEFF3.1 nuclear data library, and the modern version of the fuel rod performance code TRAFIC were used for this analysis. Because experimental data on the properties of the mixed minor-actinide oxides are scarce, and the in-reactor behaviour of the T91 steel chosen as cladding, as well as of the corrosion protective layer, is still not well-known, a set of "best estimates" provided the properties used in the code. The obtained results indicate that both fuel candidates, CERCER and CERMET, can satisfy the fuel design and safety criteria of EFIT. The residence time for both types of fuel elements can reach about 5 years with the reactivity swing within ±1000 pcm, and about 22% of the loaded MA is transmuted during this period. However, the fuel centreline temperature in the hottest CERCER fuel rod is close to the temperature above which MgO matrix becomes chemically instable. Moreover, a weak PCMI can appear in about 3 years of operation. The CERMET fuel can provide larger safety margins: the fuel temperature is more than 1000 K below the permitted level of 2380 K and the pellet-cladding gap remains open until the end of operation.

  9. Nuclear fuel activity with minor actinides after their useful life in a BWR; Actividad del combustible nuclear con actinidos menores despues de su vida util en un reactor BWR

    Energy Technology Data Exchange (ETDEWEB)

    Martinez C, E.; Ramirez S, J. R.; Alonso V, G., E-mail: eduardo.martinez@inin.gob.mx [ININ, Carretera Mexico-Toluca s/n, 52750 Ocoyoacac, Estado de Mexico (Mexico)

    2016-09-15

    Nuclear fuel used in nuclear power reactors has a life cycle, in which it provides energy, at the end of this cycle is withdrawn from the reactor core. This used fuel is known as spent nuclear fuel, a strong problem with this fuel is that when the fuel was irradiated in a nuclear reactor it leaves with an activity of approximately 1.229 x 10{sup 15} Bq. The aim of the transmutation of actinides from spent nuclear fuel is to reduce the activity of high level waste that must be stored in geological repositories and the lifetime of high level waste; these two achievements would reduce the number of necessary repositories, as well as the duration of storage. The present work is aimed at evaluating the activity of a nuclear fuel in which radioactive actinides could be recycled to remove most of the radioactive material, first establishing a reference of actinides production in the standard nuclear fuel of uranium at end of its burning in a BWR, and a fuel rod design containing 6% of actinides in an uranium matrix from the enrichment tails is proposed, then 4 standard uranium fuel rods are replaced by 4 actinide bars to evaluate the production and transmutation of the same, finally the reduction of actinide activity in the fuel is evaluated. (Author)

  10. Moessbauer spectroscopy with actinide elements

    Energy Technology Data Exchange (ETDEWEB)

    Potzel, W.; Moser, J.; Asch, L.; Kalvius, G.M. (Technische Univ. Muenchen, Garching (Germany, F.R.)

    1983-01-01

    Although formally equivalent to the lanthanide (4f) elements, the light actinides show a much more varied behaviour due to the larger spatial extent and ionizability of the 5f electrons. The application of Moessbauer spectroscopy for the determination of electronic properties of the actinides is outlined. Emphasis is put on high pressure Moessbauer experiments using the 60 keV transition in /sup 237/Np to study questions of delocalization of 5f electrons.

  11. Selection of actinide chemical analogues for WIPP tests

    Energy Technology Data Exchange (ETDEWEB)

    Villarreal, R.; Spall, D.

    1995-07-05

    The Department of Energy must demonstrate the effectiveness of the Waste Isolation Pilot Plant (WIPP) as a permanent repository for the disposal of transuranic (TRU) waste. Performance assessments of the WIPP require that estimates of the transportability and outcome of the radionuclides (actinides) be determined from disposal rooms that may become either partially or completely filled with brine. Federal regulations limit the amount of radioactivity that may be unintentionally released to the accessible environment by any mechanism during the post closure phase up to 10,000 years. Thermodynamic models have been developed to predict the concentrations of actinides in the WIPP disposal rooms under various situations and chemical conditions. These models are based on empirical and theoretical projections of the chemistry that might be present in and around the disposal room zone for both near and long-term periods. The actinides that are known to be present in the TRU wastes (and are included in the model) are Th, U, Np, Pu, and Am. Knowledge of the chemistry that might occur in the disposal rooms when the waste comes in contact with brine is important in understanding the range of oxidation states that might be present under different conditions. There is a need to establish the mechanisms and resultant rate of transport, migration, or effective retardation of actinides beyond the disposal rooms to the boundary of the accessible environment. The influence of the bulk salt rock, clay sediments and other geologic matrices on the transport behavior of actinides must be determined to establish the overall performance and capability of the WIPP in isolating waste from the environment. Tests to determine the capabilities of the WIPP geologic formations in retarding actinide species in several projected oxidation states would provide a means to demonstrate the effectiveness of the WIPP in retaining TRU wastes.

  12. A Fast Numerical Method for the Calculation of the Equilibrium Isotopic Composition of a Transmutation System in an Advanced Fuel Cycle

    Directory of Open Access Journals (Sweden)

    F. Álvarez-Velarde

    2012-01-01

    Full Text Available A fast numerical method for the calculation in a zero-dimensional approach of the equilibrium isotopic composition of an iteratively used transmutation system in an advanced fuel cycle, based on the Banach fixed point theorem, is described in this paper. The method divides the fuel cycle in successive stages: fuel fabrication, storage, irradiation inside the transmutation system, cooling, reprocessing, and incorporation of the external material into the new fresh fuel. The change of the fuel isotopic composition, represented by an isotope vector, is described in a matrix formulation. The resulting matrix equations are solved using direct methods with arbitrary precision arithmetic. The method has been successfully applied to a double-strata fuel cycle with light water reactors and accelerator-driven subcritical systems. After comparison to the results of the EVOLCODE 2.0 burn-up code, the observed differences are about a few percents in the mass estimations of the main actinides.

  13. Statistical transmutation in doped quantum dimer models.

    Science.gov (United States)

    Lamas, C A; Ralko, A; Cabra, D C; Poilblanc, D; Pujol, P

    2012-07-06

    We prove a "statistical transmutation" symmetry of doped quantum dimer models on the square, triangular, and kagome lattices: the energy spectrum is invariant under a simultaneous change of statistics (i.e., bosonic into fermionic or vice versa) of the holes and of the signs of all the dimer resonance loops. This exact transformation enables us to define the duality equivalence between doped quantum dimer Hamiltonians and provides the analytic framework to analyze dynamical statistical transmutations. We investigate numerically the doping of the triangular quantum dimer model with special focus on the topological Z(2) dimer liquid. Doping leads to four (instead of two for the square lattice) inequivalent families of Hamiltonians. Competition between phase separation, superfluidity, supersolidity, and fermionic phases is investigated in the four families.

  14. Transmutation Fuel Campaign Description and Status

    Energy Technology Data Exchange (ETDEWEB)

    Jon Carmack; Kemal O. Pasamehmetoglu

    2008-01-01

    This report contains a technical summary package in response to a Level 2 milestone in the transmutation fuel campaign (TFC) management work-package calling for input to the Secretarial decision. At present, the form of the Secretarial decision package is not fully defined, and it is not clear exactly what will be required from the TFC as a final input. However, it is anticipated that a series oftechnical and programmatic documents will need to be provided in support of a wider encompassing document on GNEP technology development activities. The TFC technical leadership team provides this report as initial input to the secretarial decision package which is being developed by the Technical Integration Office (TIO) in support of Secretarial decision. This report contains a summary of the TFC execution plan with a work breakdown structure, highlevel schedule, major milestones, and summary description of critical activities in support of campaign objectives. Supporting documents referenced in this report but provided under separate cover include: • An updated review of the state-of-the art for transmutation fuel development activities considering national as well as international fuel research and development testing activities. • A definition of the Technology Readiness Level (TRL) used to systematically define and execute the transmutation fuel development activities.

  15. Can transmutation replace deep radioactive repositories?; Ersetzt Transmutation die Tiefenlagerung radioaktiver Abfaelle?

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2013-03-15

    This illustrated brief report issued by the Swiss Federal Nuclear Safety Inspectorate (ENSI) takes a look at transmutation - a method to reduce the time taken for the radioactivity of radioactive wastes to decay. The aim of such a reduction is to reduce the amount of space needed for special underground repositories for highly radioactive wastes. Transmutation is briefly described. Nuclear fuel cycles with spent fuel separation and reprocessing is examined. The large-scale feasibility of such methods is looked at and the advantages offered in connection with the design and implementation of deep nuclear waste repositories are discussed.

  16. Can transmutation replace deep radioactive repositories?; Ersetzt Transmutation die Tiefenlagerung radioaktiver Abfaelle?

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2013-03-15

    This illustrated brief report issued by the Swiss Federal Nuclear Safety Inspectorate (ENSI) takes a look at transmutation - a method to reduce the time taken for the radioactivity of radioactive wastes to decay. The aim of such a reduction is to reduce the amount of space needed for special underground repositories for highly radioactive wastes. Transmutation is briefly described. Nuclear fuel cycles with spent fuel separation and reprocessing is examined. The large-scale feasibility of such methods is looked at and the advantages offered in connection with the design and implementation of deep nuclear waste repositories are discussed.

  17. 33rd Actinide Separations Conference

    Energy Technology Data Exchange (ETDEWEB)

    McDonald, L M; Wilk, P A

    2009-05-04

    Welcome to the 33rd Actinide Separations Conference hosted this year by the Lawrence Livermore National Laboratory. This annual conference is centered on the idea of networking and communication with scientists from throughout the United States, Britain, France and Japan who have expertise in nuclear material processing. This conference forum provides an excellent opportunity for bringing together experts in the fields of chemistry, nuclear and chemical engineering, and actinide processing to present and discuss experiences, research results, testing and application of actinide separation processes. The exchange of information that will take place between you, and other subject matter experts from around the nation and across the international boundaries, is a critical tool to assist in solving both national and international problems associated with the processing of nuclear materials used for both defense and energy purposes, as well as for the safe disposition of excess nuclear material. Granlibakken is a dedicated conference facility and training campus that is set up to provide the venue that supports communication between scientists and engineers attending the 33rd Actinide Separations Conference. We believe that you will find that Granlibakken and the Lake Tahoe views provide an atmosphere that is stimulating for fruitful discussions between participants from both government and private industry. We thank the Lawrence Livermore National Laboratory and the United States Department of Energy for their support of this conference. We especially thank you, the participants and subject matter experts, for your involvement in the 33rd Actinide Separations Conference.

  18. Monte Carlo analysis of the long-lived fission product neutron capture rates at the Transmutation by Adiabatic Resonance Crossing (TARC) experiment

    Energy Technology Data Exchange (ETDEWEB)

    Abanades, A., E-mail: abanades@etsii.upm.es [Grupo de Modelizacion de Sistemas Termoenergeticos, ETSII, Universidad Politecnica de Madrid, c/Ramiro de Maeztu, 7, 28040 Madrid (Spain); Alvarez-Velarde, F.; Gonzalez-Romero, E.M. [Centro de Investigaciones Medioambientales y Tecnologicas (CIEMAT), Avda. Complutense, 40, Ed. 17, 28040 Madrid (Spain); Ismailov, K. [Tokyo Institute of Technology, 2-12-1, O-okayama, Meguro-ku, Tokyo 152-8550 (Japan); Lafuente, A. [Grupo de Modelizacion de Sistemas Termoenergeticos, ETSII, Universidad Politecnica de Madrid, c/Ramiro de Maeztu, 7, 28040 Madrid (Spain); Nishihara, K. [Transmutation Section, J-PARC Center, JAEA, Tokai-mura, Ibaraki-ken 319-1195 (Japan); Saito, M. [Tokyo Institute of Technology, 2-12-1, O-okayama, Meguro-ku, Tokyo 152-8550 (Japan); Stanculescu, A. [International Atomic Energy Agency (IAEA), Vienna (Austria); Sugawara, T. [Transmutation Section, J-PARC Center, JAEA, Tokai-mura, Ibaraki-ken 319-1195 (Japan)

    2013-01-15

    Highlights: Black-Right-Pointing-Pointer TARC experiment benchmark capture rates results. Black-Right-Pointing-Pointer Utilization of updated databases, included ADSLib. Black-Right-Pointing-Pointer Self-shielding effect in reactor design for transmutation. Black-Right-Pointing-Pointer Effect of Lead nuclear data. - Abstract: The design of Accelerator Driven Systems (ADS) requires the development of simulation tools that are able to describe in a realistic way their nuclear performance and transmutation rate capability. In this publication, we present an evaluation of state of the art Monte Carlo design tools to assess their performance concerning transmutation of long-lived fission products. This work, performed under the umbrella of the International Atomic Energy Agency, analyses two important aspects for transmutation systems: moderation on Lead and neutron captures of {sup 99}Tc, {sup 127}I and {sup 129}I. The analysis of the results shows how shielding effects due to the resonances at epithermal energies of these nuclides affects strongly their transmutation rate. The results suggest that some research effort should be undertaken to improve the quality of Iodine nuclear data at epithermal and fast neutron energy to obtain a reliable transmutation estimation.

  19. Calculation of cohesive energy of actinide metals

    Institute of Scientific and Technical Information of China (English)

    钱存富; 陈秀芳; 余瑞璜; 耿平; 段占强

    1997-01-01

    According to empirical electron theory of solids and molecules (EET), an equation for calculating the cohesive energy of actinide metals is given, the cohesive energy of 9 actinide metals with known crystal structure is calculated, which is identical with the experimental values on the whole, and the cohesive energy of 6 actinide metals with unknown crystal structure is forecast.

  20. Minor Actinides Loading Optimization for Proliferation Resistant Fuel Design - BWR

    Energy Technology Data Exchange (ETDEWEB)

    G. S. Chang; Hongbin Zhang

    2009-09-01

    One approach to address the United States Nuclear Power (NP) 2010 program for the advanced light water reactor (LWR) (Gen-III+) intermediate-term spent fuel disposal need is to reduce spent fuel storage volume while enhancing proliferation resistance. One proposed solution includes increasing burnup of the discharged spent fuel and mixing minor actinide (MA) transuranic nuclides (237Np and 241Am) in the high burnup fuel. Thus, we can reduce the spent fuel volume while increasing the proliferation resistance by increasing the isotopic ratio of 238Pu/Pu. For future advanced nuclear systems, MAs are viewed more as a resource to be recycled, and transmuted to less hazardous and possibly more useful forms, rather than simply disposed of as a waste stream in an expensive repository facility. MAs play a much larger part in the design of advanced systems and fuel cycles, not only as additional sources of useful energy, but also as direct contributors to the reactivity control of the systems into which they are incorporated. A typical boiling water reactor (BWR) fuel unit lattice cell model with UO2 fuel pins will be used to investigate the effectiveness of adding MAs (237Np and/or 241Am) to enhance proliferation resistance and improve fuel cycle performance for the intermediate-term goal of future nuclear energy systems. However, adding MAs will increase plutonium production in the discharged spent fuel. In this work, the Monte-Carlo coupling with ORIGEN-2.2 (MCWO) method was used to optimize the MA loading in the UO2 fuel such that the discharged spent fuel demonstrates enhanced proliferation resistance, while minimizing plutonium production. The axial averaged MA transmutation characteristics at different burnup were compared and their impact on neutronics criticality and the ratio of 238Pu/Pu discussed.

  1. Actinides and Life's Origins.

    Science.gov (United States)

    Adam, Zachary

    2007-12-01

    There are growing indications that life began in a radioactive beach environment. A geologic framework for the origin or support of life in a Hadean heavy mineral placer beach has been developed, based on the unique chemical properties of the lower-electronic actinides, which act as nuclear fissile and fertile fuels, radiolytic energy sources, oligomer catalysts, and coordinating ions (along with mineralogically associated lanthanides) for prototypical prebiotic homonuclear and dinuclear metalloenzymes. A four-factor nuclear reactor model was constructed to estimate how much uranium would have been required to initiate a sustainable fission reaction within a placer beach sand 4.3 billion years ago. It was calculated that about 1-8 weight percent of the sand would have to have been uraninite, depending on the weight percent, uranium enrichment, and quantity of neutron poisons present within the remaining placer minerals. Radiolysis experiments were conducted with various solvents with the use of uraniumand thorium-rich minerals (metatorbernite and monazite, respectively) as proxies for radioactive beach sand in contact with different carbon, hydrogen, oxygen, and nitrogen reactants. Radiation bombardment ranged in duration of exposure from 3 weeks to 6 months. Low levels of acetonitrile (estimated to be on the order of parts per billion in concentration) were conclusively identified in 2 setups and tentatively indicated in a 3(rd) by gas chromatography/mass spectrometry. These low levels have been interpreted within the context of a Hadean placer beach prebiotic framework to demonstrate the promise of investigating natural nuclear reactors as power production sites that might have assisted the origins of life on young rocky planets with a sufficiently differentiated crust/mantle structure. Future investigations are recommended to better quantify the complex relationships between energy release, radioactive grain size, fissionability, reactant phase, phosphorus

  2. Actinides and Life's Origins

    Science.gov (United States)

    Adam, Zachary

    2007-12-01

    There are growing indications that life began in a radioactive beach environment. A geologic framework for the origin or support of life in a Hadean heavy mineral placer beach has been developed, based on the unique chemical properties of the lower-electronic actinides, which act as nuclear fissile and fertile fuels, radiolytic energy sources, oligomer catalysts, and coordinating ions (along with mineralogically associated lanthanides) for prototypical prebiotic homonuclear and dinuclear metalloenzymes. A four-factor nuclear reactor model was constructed to estimate how much uranium would have been required to initiate a sustainable fission reaction within a placer beach sand 4.3 billion years ago. It was calculated that about 1-8 weight percent of the sand would have to have been uraninite, depending on the weight percent, uranium enrichment, and quantity of neutron poisons present within the remaining placer minerals. Radiolysis experiments were conducted with various solvents with the use of uranium- and thorium-rich minerals (metatorbernite and monazite, respectively) as proxies for radioactive beach sand in contact with different carbon, hydrogen, oxygen, and nitrogen reactants. Radiation bombardment ranged in duration of exposure from 3 weeks to 6 months. Low levels of acetonitrile (estimated to be on the order of parts per billion in concentration) were conclusively identified in 2 setups and tentatively indicated in a 3rd by gas chromatography/mass spectrometry. These low levels have been interpreted within the context of a Hadean placer beach prebiotic framework to demonstrate the promise of investigating natural nuclear reactors as power production sites that might have assisted the origins of life on young rocky planets with a sufficiently differentiated crust/mantle structure. Future investigations are recommended to better quantify the complex relationships between energy release, radioactive grain size, fissionability, reactant phase, phosphorus

  3. A Study on the Kinetic Characteristics of Transmutation Process Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Chung, Chang Hyun; You, Young Woo; Cho, Jae seon; Huh, Chang Wook; Kim, Doh Hyung [Seoul National University, Seoul (Korea, Republic of)

    1997-07-01

    The purpose of this study is to examine the transient heat transfer characteristics of liquid mental as the coolant used in accelerator-driven transmutation process reactor which is related the disposal of high-level radioactive nuclide. At current stage, the accelerator-driven transmutation process is investigated as the most appropriate method among many transmutation process methods. In this study, previous research works are investigated especially about the thermal hydraulics and kinetic behavior of coolant material including heat transfer of coolant in transmutation process reactor. A study on the heat transfer characteristics of liquid metal is performed based on the thermal hydraulic kinetic characteristics of liquid metal reactor which uses liquid metal coolant. Based on this study, the most appropriate material for the coolant of transmutation reactor will be recommended. 53 refs., 15 tabs., 33 figs. (author)

  4. Preliminary considerations concerning actinide solubilities

    Energy Technology Data Exchange (ETDEWEB)

    Newton, T.W.; Bayhurst, B.P.; Daniels, W.R.; Erdal, B.R.; Ogard, A.E.

    1980-01-01

    Work at the Los Alamos Scientific Laboratory on the fundamental solution chemistry of the actinides has thus far been confined to preliminary considerations of the problems involved in developing an understanding of the precipitation and dissolution behavior of actinide compounds under environmental conditions. Attempts have been made to calculate solubility as a function of Eh and pH using the appropriate thermodynamic data; results have been presented in terms of contour maps showing lines of constant solubility as a function of Eh and pH. Possible methods of control of the redox potential of rock-groundwater systems by the use of Eh buffers (redox couples) is presented.

  5. Neutron-transmutation-doped germanium bolometers

    Science.gov (United States)

    Palaio, N. P.; Rodder, M.; Haller, E. E.; Kreysa, E.

    1983-01-01

    Six slices of ultra-pure germanium were irradiated with thermal neutron fluences between 7.5 x 10 to the 16th and 1.88 x 10 to the 18th per sq cm. After thermal annealing the resistivity was measured down to low temperatures (less than 4.2 K) and found to follow the relationship rho = rho sub 0 exp(Delta/T) in the hopping conduction regime. Also, several junction FETs were tested for noise performance at room temperature and in an insulating housing in a 4.2 K cryostat. These FETs will be used as first stage amplifiers for neutron-transmutation-doped germanium bolometers.

  6. Statistical Transmutation in Floquet Driven Optical Lattices.

    Science.gov (United States)

    Sedrakyan, Tigran A; Galitski, Victor M; Kamenev, Alex

    2015-11-06

    We show that interacting bosons in a periodically driven two dimensional (2D) optical lattice may effectively exhibit fermionic statistics. The phenomenon is similar to the celebrated Tonks-Girardeau regime in 1D. The Floquet band of a driven lattice develops the moat shape, i.e., a minimum along a closed contour in the Brillouin zone. Such degeneracy of the kinetic energy favors fermionic quasiparticles. The statistical transmutation is achieved by the Chern-Simons flux attachment similar to the fractional quantum Hall case. We show that the velocity distribution of the released bosons is a sensitive probe of the fermionic nature of their stationary Floquet state.

  7. The FUTURIX - transmutation experiment in Phenix

    Energy Technology Data Exchange (ETDEWEB)

    Warin, D.; Sudreau, F.; Pillon, S.; Drin, N.; Donnet, L.; Brunon, E

    2004-07-01

    In support to the European and American strategies of long-live radioactive waste transmutation in GEN IV critical fast neutron reactors or ADS, an irradiation test of fuels with high contents of transuranium elements is being designed and will be irradiated during the two last cycles of the Phenix fast reactor. This experiment will provide the main data concerning the behaviour under irradiation in representative conditions of different innovative fuels (oxides, nitrides, metal alloys, cermets) and will allow qualification and validation of models developed to predict their performance. (authors)

  8. Actinide fission and capture cross section measurements at ILL: the Mini-INCA project

    Energy Technology Data Exchange (ETDEWEB)

    Letourneau, A.; Bringer, O.; Chabod, S.; Fioni, G.; Foucher, Y.; Marie, F.; Veyssiere, Ch. [CEA/Saclay/DSM/DAPNIA - Gif-sur-Yvette (France); Mahamid, I. Al. [Lawrence Berkeley National Laboratory, E.H. and S division, Berkeley CA (United States); Blandin, Ch. [CEA/Cadarache/DEN/DER/SPEX - Saint-Paul-lez-Durances (France); Chartier, F. [CEA/Saclay/DEN/DPC/SECR - Gif-sur-Yvette (France); Faust, H.; Mutti, P. [Institut Laue-Langevin, BP 156, F-38042 Grenoble Cedex 9 (France)

    2005-07-01

    Fission cross section of short-lived minor actinides is of prime importance for the incineration of minor actinides in high and thermal neutron fluxes. But due to the shortness of their half-lives, measurements are difficult to handle on these isotopes and the existing data present some large discrepancies. An original method has been developed, in the framework of the Mini-INCA project at ILL, to measure the fission and capture cross sections of minor actinides with low error bars associated even for short-lived isotopes. This method lies on a quasi on-line alpha- and gamma-spectroscopy of irradiated samples and on the use of fission micro-chambers. Coupled to a very powerful Monte-Carlo simulation, both microscopic information on nuclear reactions (total and partial cross sections for neutron capture and/or fission reactions) and macroscopic information on transmutation and incineration potentials could be gathered. In this paper, the method is explained in its originality and some recent results are given and compared with existing measurements and evaluated data libraries. (authors)

  9. Physical studies of transmutation scenarios. The Muse program with the Masurca facility: a step towards an hybrid demonstrator?; Etudes physiques des scenarios de transmutation. Le programme Muse dans Masurca: une etape vers un demonstrateur hybride?

    Energy Technology Data Exchange (ETDEWEB)

    Bouchard, J. [CEA Saclay, Dir. de l' Energie Nucleaire DEN, 91 - Gif sur Yvette (France); Leconte, Ph. [CEA 75 - Paris (France); Doubre, H. [Centre National de la Recherche Scientifique (CNRS), 75 - Paris (France); Bhatnagar, V.P. [European Commission Brussels (Belgium); Carbonnier, J.L. [CEA Cadarache, Dir. de l' Energie Nucleaire DEN, 13 - Saint Paul lez Durance (France); Chawla, R. [Ecole Polytechnique Federale de Lausanne, LRS, PSI (Switzerland); Bernard, H. [CEA Cadarache, 13 - Saint Paul lez Durance (France)

    2002-07-01

    The Muse research program, which started in 1995, is a contribution to the development of a dedicated subcritical accelerator driven system (ADS) for the transmutation of minor actinides produced by conventional nuclear power plants. The Muse experiments aim at making a parametric study of different reactor core compositions with different subcritical levels and supplied by different sources in order to demonstrate that the measurement techniques and the calculation charts established for critical FBRs remain valid with an hybrid system. The 4. phase of the Muse program concerns the design, realization and installation of the Genepi (generator of intense pulse neutrons) deutons accelerator at the Masurca facility of Cadarache (France) for the understanding of the neutronic behaviour of an ADS, the definition of a reference calculation scheme, and the development of specific experimental techniques for dynamical measurements. This document brings together the presentations (transparencies) given at the SFEN technical meeting of May 30, 2002 about the Muse program. (J.S.)

  10. Development of a remote bushing for actinide vitrification

    Energy Technology Data Exchange (ETDEWEB)

    Schumacher, R.F.; Ramsey, W.G.; Johnson, F.M. [and others

    1996-12-31

    The Savannah River Site (SRS) and the Savannah River Technology Center (SRTC) are combining their existing experience in handling highly radioactive, special nuclear materials with commercial glass fiberization technology in order to assemble a small vitrification system for radioactive actinide solutions. The vitrification system or {open_quotes}brushing{close_quotes}, is fabricated from platinum-rhodium alloy and is based on early marble remelt fiberization technology. Advantages of this unique system include its relatively small size, reliable operation, geometrical safety (nuclear criticality), and high temperature capability. The bushing design should be capable of vitrifying a number of the actinide nuclear materials, including solutions of americium/curium, neptunium, and possibly plutonium. State of the art, mathematical and oil model studies are being combined with basic engineering evaluations to verify and improve the thermal and mechanical design concepts.

  11. 4th Neutron Transmutation Doping Conference

    CERN Document Server

    1984-01-01

    viii The growing use of NTD silicon outside the U. S. A. motivated an interest in having the next NTD conference in Europe. Therefore, the Third International Conference on Neutron Transmutation-Doped Silicon was organized by Jens Guldberg and held in Copenhagen, Denmark on August 27-29, 1980. The papers presented at this conference reviewed the developments which occurred during the t'A'O years since the previous conference and included papers on irradiation technology, radiation-induced defects, characteriza­ tion of NTD silicon, and the use of NTD silicon for device appli­ cations. The proceedings of this conference were edited by Jens Guldberg and published by Plenum Press in 1981. Interest in, and commercial use of, NTD silicon continued to grow after the Third NTD Conference, and research into neutron trans­ mutation doping of nonsilicon semiconductors had begun to accel­ erate. The Fourth International Transmutation Doping Conference reported in this volume includes invited papers summarizing the p...

  12. Environmental research on actinide elements

    Energy Technology Data Exchange (ETDEWEB)

    Pinder, J.E. III; Alberts, J.J.; McLeod, K.W.; Schreckhise, R.G. (eds.)

    1987-08-01

    The papers synthesize the results of research sponsored by DOE's Office of Health and Environmental Research on the behavior of transuranic and actinide elements in the environment. Separate abstracts have been prepared for the 21 individual papers. (ACR)

  13. Recycling option search for a 600-MWe sodium-cooled transmutation fast reactor

    Directory of Open Access Journals (Sweden)

    Yong Kyo Lee

    2015-02-01

    Full Text Available Four recycling scenarios involving pyroprocessing of spent fuel (SF have been investigated for a 600-MWe transmutation sodium-cooled fast reactor (SFR, KALIMER. Performance evaluation was done with code system REBUS connected with TRANSX and TWODANT. Scenario Number 1 is the pyroprocessing of Canada deuterium uranium (CANDU SF. Because the recycling of CANDU SF does not have any safety problems, the CANDU-Pyro-SFR system will be possible if the pyroprocessing capacity is large enough. Scenario Number 2 is a feasibility test of feed SF from a pressurized water reactor PWR. The sensitivity of cooling time before prior to pyro-processing was studied. As the cooling time increases, excess reactivity at the beginning of the equilibrium cycle (BOEC decreases, thereby creating advantageous reactivity control and improving the transmutation performance of minor actinides. Scenario Number 3 is a case study for various levels of recovery factors of transuranic isotopes (TRUs. If long-lived fission products can be separated during pyroprocessing, the waste that is not recovered is classified as low- and intermediate-level waste, and it is sufficient to be disposed of in an underground site due to very low-heat-generation rate when the waste cooling time becomes >300 years at a TRU recovery factor of 99.9%. Scenario Number 4 is a case study for the recovery factor of rare earth (RE isotopes. The RE isotope recovery factor should be lowered to ≤20% in order to make sodium void reactivity less than <7$, which is the design limit of a metal fuel.

  14. Accurate determination of Curium and Californium isotopic ratios by inductively coupled plasma quadrupole mass spectrometry (ICP-QMS) in 248Cm samples for transmutation studies

    Energy Technology Data Exchange (ETDEWEB)

    Gourgiotis, A.; Isnard, H.; Aubert, M.; Dupont, E.; AlMahamid, I.; Cassette, P.; Panebianco, S.; Letourneau, A.; Chartier, F.; Tian, G.; Rao, L.; Lukens, W.

    2011-02-01

    The French Atomic Energy Commission has carried out several experiments including the mini-INCA (INcineration of Actinides) project for the study of minor-actinide transmutation processes in high intensity thermal neutron fluxes, in view of proposing solutions to reduce the radiotoxicity of long-lived nuclear wastes. In this context, a Cm sample enriched in {sup 248}Cm ({approx}97 %) was irradiated in thermal neutron flux at the High Flux Reactor (HFR) of the Laue-Langevin Institute (ILL). This work describes a quadrupole ICP-MS (ICP-QMS) analytical procedure for precise and accurate isotopic composition determination of Cm before sample irradiation and of Cm and Cf after sample irradiation. The factors that affect the accuracy and reproducibility of isotopic ratio measurements by ICP-QMS, such as peak centre correction, detector dead time, mass bias, abundance sensitivity and hydrides formation, instrumental background, and memory blank were carefully evaluated and corrected. Uncertainties of the isotopic ratios, taking into account internal precision of isotope ratio measurements, peak tailing, and hydrides formations ranged from 0.3% to 1.3%. This uncertainties range is quite acceptable for the nuclear data to be used in transmutation studies.

  15. Accurate determination of Curium and Californium isotopic ratios by inductively coupled plasma quadrupole mass spectrometry (ICP-QMS) in Cm-{sup 248} samples for transmutation studies

    Energy Technology Data Exchange (ETDEWEB)

    Gourgiotis, A.; Isnard, H.; Aubert, M. [CEA Saclay, DEN DPC SECR LANIE, F-91191 Gif Sur Yvette (France); Dupont, E.; Panebianco, S.; Letourneau, A. [CEA Saclay, DSM IRFU SPhN, F-91191 Gif Sur Yvette, (France); AlMahamid, I. [New York State Dept Hlth, Wadsworth Ctr, Albany, NY 12201 (United States); AlMahamid, I. [SUNY Albany, Sch Publ Hlth, Albany, NY 12222 (United States); Cassette, P. [CEA Saclay, LIST, Lab Natl Henri Becquerel LNE LNHB, F-91191 Gif Sur Yvette (France); Chartier, F. [CEA Saclay, DEN DPC, F-91191 Gif Sur Yvette (France); Tiang, G.; Rao, L.; Lukens, W. [Lawrence Berkeley Lab, Div Chem Sci, Berkeley, CA 94720 (United States)

    2010-07-01

    The French Atomic Energy Commission has carried out several experiments including the mini-INCA (Incineration of Actinides) project for the study of minor-actinide transmutation processes in high intensity thermal neutron fluxes, in view of proposing solutions to reduce the radiotoxicity of long-lived nuclear wastes. In this context, a Cm sample enriched in {sup 248}Cm (similar to 97%) was irradiated in thermal neutron flux at the High Flux Reactor (HFR) of the Laue-Langevin Institute (ILL). This work describes a quadrupole ICP-MS (ICP-QMS) analytical procedure for precise and accurate isotopic composition determination of Cm before sample irradiation and of Cm and Cf after sample irradiation. The factors that affect the accuracy and reproducibility of isotopic ratio measurements by ICP-QMS, such as peak centre correction, detector dead time, mass bias, abundance sensitivity and hydrides formation, instrumental background, and memory blank were carefully evaluated and corrected. Uncertainties of the isotopic ratios, taking into account internal precision of isotope ratio measurements, peak tailing, and hydrides' formations ranged from 0. 3% to 1. 3%. This uncertainties' range is quite acceptable for the nuclear data to be used in transmutation studies. (authors)

  16. Fast reactor core concepts to improve transmutation efficiency

    Energy Technology Data Exchange (ETDEWEB)

    Fujimura, Koji; Kawashima, Katsuyuki [Hitachi Research Laboratory, Hitachi, Ltd., 7-1-1, Omika-cho, Hitachi-shi, Ibaraki, 319-1221 Japan (Japan); Itooka, Satoshi [Hitachi-GE Nuclear Energy, Ltd., 3-1-1, Saiwai-cho, Hitachi-shi, Ibaraki, 317-0073 Japan (Japan)

    2015-12-31

    Fast Reactor (FR) core concepts to improve transmutation efficiency were conducted. A heterogeneous MA loaded core was designed based on the 1000MWe-ABR breakeven core. The heterogeneous MA loaded core with Zr-H loaded moderated targets had a better transmutation performance than the MA homogeneous loaded core. The annular pellet rod design was proposed as one of the possible design options for the MA target. It was shown that using annular pellet MA rods mitigates the self-shielding effect in the moderated target so as to enhance the transmutation rate.

  17. Infrared absorption study of neutron-transmutation-doped germanium

    Science.gov (United States)

    Park, I. S.; Haller, E. E.

    1988-01-01

    Using high-resolution far-infrared Fourier transform absorption spectroscopy and Hall effect measurements, the evolution of the shallow acceptor and donor impurity levels in germanium during and after the neutron transmutation doping process was studied. The results show unambiguously that the gallium acceptor level concentration equals the concentration of transmutated Ge-70 atoms during the whole process indicating that neither recoil during transmutation nor gallium-defect complex formation play significant roles. The arsenic donor levels appear at full concentration only after annealing for 1 h at 450 C. It is shown that this is due to donor-radiation-defect complex formation. Again, recoil does not play a significant role.

  18. Monte Carlo calculations on transmutation of trans-uranic nuclear waste isotopes using spallation neutrons difference of lead and graphite moderators

    CERN Document Server

    Hashemi-Nezhad, S R; Brandt, R; Krivopustov, M I; Kulakov, B A; Odoj, R; Sosnin, A N; Wan, J S; Westmeier, W

    2002-01-01

    Transmutation rates of sup 2 sup 3 sup 9 Pu and some minor actinides ( sup 2 sup 3 sup 7 Np, sup 2 sup 4 sup 1 Am, sup 2 sup 4 sup 5 Cm and sup 2 sup 4 sup 6 Cm), in two accelerator-driven systems (ADS) with lead or graphite moderating environments, were calculated using the LAHET code system. The ADS that were used had a large volume (approx 32 m sup 3) and contained no fissile material, except for a small amount of fissionable waste nuclei that existed in some cases. Calculations were performed at an incident proton energy of 1.5 GeV and the spallation target was lead. Also breeding rates of sup 2 sup 3 sup 9 Pu and sup 2 sup 3 sup 3 U as well as the transmutation rates of two long-lived fission products sup 9 sup 9 Tc and sup 1 sup 2 sup 9 I were calculated at different locations in the moderator. It is shown that an ADS with graphite moderator is a much more effective transmuter than that with lead moderator.

  19. Actinide cation-cation complexes

    Energy Technology Data Exchange (ETDEWEB)

    Stoyer, Nancy Jane [Univ. of California, Berkeley, CA (United States)

    1994-12-01

    The +5 oxidation state of U, Np, Pu, and Am is a linear dioxo cation (AnO2+) with a formal charge of +1. These cations form complexes with a variety of other cations, including actinide cations. Other oxidation states of actinides do not form these cation-cation complexes with any cation other than AnO2+; therefore, cation-cation complexes indicate something unique about AnO2+ cations compared to actinide cations in general. The first cation-cation complex, NpO2+•UO22+, was reported by Sullivan, Hindman, and Zielen in 1961. Of the four actinides that form AnO2+ species, the cation-cation complexes of NpO2+ have been studied most extensively while the other actinides have not. The only PuO2+ cation-cation complexes that have been studied are with Fe3+ and Cr3+ and neither one has had its equilibrium constant measured. Actinides have small molar absorptivities and cation-cation complexes have small equilibrium constants; therefore, to overcome these obstacles a sensitive technique is required. Spectroscopic techniques are used most often to study cation-cation complexes. Laser-Induced Photacoustic Spectroscopy equilibrium constants for the complexes NpO2+•UO22+, NpO2+•Th4+, PuO2+•UO22+, and PuO2+•Th4+ at an ionic strength of 6 M using LIPAS are 2.4 ± 0.2, 1.8 ± 0.9, 2.2 ± 1.5, and ~0.8 M-1.

  20. Pyrometallurgical process of actinide metal

    Energy Technology Data Exchange (ETDEWEB)

    Yoo, Jae Hyung; Kang, Young Ho; Woo, Mun Sik; Hwang, Sung Chan

    1999-06-01

    Major subject on pyrometallurgical partitioning technology is to separate transmutation elements (TRU) from rare earth elements(RE). Distribution coefficients of TRU and RE between molten chloride and liquid cadmium were measured for reductive extraction, and TRU were separated from RE in simplified molten chloride system by electrorefining. And separation efficiency between TRU and RE were estimated by using thermodynamics data. The results indicate that uranium, neptunium and plutonium are easy to separate from RE but some amount of RE accompany americium, and that processes have to be optimized to attain good separation efficiency of TRU. (author)

  1. Fuels and Materials for Transmutation: A Status Report No 402

    National Research Council Canada - National Science Library

    2005-01-01

    This status report, produced by the subgroup on fuels and materials, describes state-of-the-art technology concerning fuels and materials for transmutation, provides information on the availability...

  2. Transmutation of silicon carbide in fusion nuclear environment

    Energy Technology Data Exchange (ETDEWEB)

    Sawan, M.E., E-mail: sawan@engr.wisc.edu [University of Wisconsin-Madison, 1500 Engineering Dr., Madison, WI (United States); Katoh, Y.; Snead, L.L. [Oak Ridge National Laboratory, Oak Ridge, TN (United States)

    2013-11-15

    The amount and type of metallic transmutants produced in SiC/SiC when used in magnetic (MFE) and inertial (IFE) confinement fusion systems are determined and compared to those obtained following irradiation in fission reactors. Up to ∼1.3% metallic transmutants are generated at the expected lifetime of the fusion blanket. Irradiation in fission reactors to the same fast neutron fluence produces about an order of magnitude lower metallic transmutation products than in fusion systems. While the dominant component in fusion systems is Mg, P is the main transmutation product in fission reactors. The impact on the SiC/SiC properties is not fully understood. The results of this work will help guide irradiation experiments in fission reactors to properly simulate the conditions in fusion systems by possible ion implantation. In addition, the results represent a necessary input for modeling activities aimed at understanding the expected effects on properties.

  3. One-electron physics of the actinides

    Science.gov (United States)

    Toropova, A.; Marianetti, C. A.; Haule, K.; Kotliar, G.

    2007-10-01

    We present a detailed analysis of the one-electron physics of the actinides. Various linear muffin-tin orbital basis sets are analyzed in order to determine a robust bare Hamiltonian for the actinides. The hybridization between f and spd states is compared with the f-f hopping in order to understand the Anderson-like and Hubbard-like contributions to itineracy in the actinides. We show that both contributions decrease strongly as one moves from the light actinides to the heavy actinides, while the Anderson-like contribution dominates in all cases. A real-space analysis of the band structure shows that nearest-neighbor hopping dominates the physics in these materials. Finally, we discuss the implications of our results to the delocalization transition as a function of atomic number across the actinide series.

  4. NMR studies of actinide dioxides

    Energy Technology Data Exchange (ETDEWEB)

    Tokunaga, Y. [Advanced Science Research Center, Japan Atomic Energy Agency, Tokai, Ibaraki 319-1195 (Japan)], E-mail: tokunaga.yo@jaea.go.jp; Sakai, H.; Fujimoto, T.; Kambe, S.; Walstedt, R.E.; Ikushima, K.; Yasuoka, H. [Advanced Science Research Center, Japan Atomic Energy Agency, Tokai, Ibaraki 319-1195 (Japan); Aoki, D.; Homma, Y. [Institute for Materials Research, Tohoku University, Oarai, Ibaraki 311-1313 (Japan); Haga, Y.; Matsuda, T.D.; Ikeda, S.; Yamamoto, E.; Nakamura, A. [Advanced Science Research Center, Japan Atomic Energy Agency, Tokai, Ibaraki 319-1195 (Japan); Shiokawa, Y. [Institute for Materials Research, Tohoku University, Oarai, Ibaraki 311-1313 (Japan); Nakajima, K.; Arai, Y. [Department of Nuclear Energy System, Japan Atomic Energy Agency, Tokai, Ibaraki 319-1195 (Japan); Onuki, Y. [Advanced Science Research Center, Japan Atomic Energy Agency, Tokai, Ibaraki 319-1195 (Japan); Department of Physics, Osaka University, Toyonaka, Osaka 560-0043 (Japan)

    2007-10-11

    {sup 17}O NMR measurements have been performed on a series of the actinide dioxides, UO{sub 2}, NpO{sub 2} and PuO{sub 2}. Although the {sup 17}O NMR spectra in these materials are similar at higher temperatures, the low-temperature spectra present are significantly different. In UO{sub 2} we have observed a wide spectrum, forming a rectangular shape below T{sub N}=30 K. In NpO{sub 2}, on the other hand, the spectra broaden rather gradually and exhibit a two-peak structure below T{sub 0}=26 K. In PuO{sub 2}, neither spectrum broadening nor splitting has been observed. We show that these NMR spectra clearly indicate the different nature of the low-temperature magnetic ground states in these actinide compounds.

  5. Moessbauer spectroscopy of actinide intermetallics

    Energy Technology Data Exchange (ETDEWEB)

    Kalvius, G.M.; Potzel, W.; Moser, J.; Litterst, F.J.; Asch, L.; Zaenkert, J.; Potzel, U.; Kratzer, A.; Wunsch, M. (Technische Univ. Muenchen, Garching (Germany, F.R.). Fakultaet fuer Physik); Gal, J.

    1985-04-01

    Due to their wider radical extent the 5f electrons may form bands of different width and hybridization in metallic compounds of the light actinides. This leads to a broad spectrum of magnetic properties ranging from the localized magnetism of the lanthanides to the itinerant electron magnetism often found in transition metal compounds. Also, the influence of the crystalline electric field tends to be more pronounced than in rare earth compounds, but is usually not as dominant as in the 3d series. Magnetic structures and the question of 5f electron delocalization will be reviewed with respect to actinide Moessbauer data and new results will be presented. In particular the influence of applying external pressure will be discussed.

  6. Mossbauer spectroscopy of actinide intermetallics

    Energy Technology Data Exchange (ETDEWEB)

    Kalvius, G.M.; Potzel, W.; Moser, J.; Litterst, F.J.; Asch, L.; Zankert, J.; Potzel, U.; Kratzer, A.; Wunsch, M.; Gal, J.

    1984-09-01

    Due to their wider radial extend the 5f electrons may form bands of different width and hybridization in metallic compounds of the light actinides. This leads to a broad spectrum of magnetic properties ranging from the localized magnetism of the lanthanides to the itinerant electron magnetism often found in transition metal compounds. Also, the influence of the crystalline electric field tends to be more pronounced than in rare earth compounds, but is usually not as dominant as in the 3d series. Magnetic structures and the question of 5f electron delocalization are reviewed with respet to actinide Moessbauer data and new results are presented. In particular the influence of applying external pressure is discussed. 60 references, 24 figures.

  7. Transmutation of planar media singularities in a conformal cloak.

    Science.gov (United States)

    Liu, Yichao; Mukhtar, Musawwadah; Ma, Yungui; Ong, C K

    2013-11-01

    Invisibility cloaking based on optical transformation involves materials singularity at the branch cut points. Many interesting optical devices, such as the Eaton lens, also require planar media index singularities in their implementation. We show a method to transmute two singularities simultaneously into harmless topological defects formed by anisotropic permittivity and permeability tensors. Numerical simulation is performed to verify the functionality of the transmuted conformal cloak consisting of two kissing Maxwell fish eyes.

  8. Transmutation research in Europe: Steps towards a demonstrator

    Energy Technology Data Exchange (ETDEWEB)

    Knebel, Joachim U.; Fazio, Concetta; Struwe, Dankward [Forschungszentrum Karlsruhe (FZK), Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Lepoldshafen (Germany); Abderrahim, Hamid Ait; D' hondt, Pierre [SCK-CEN, Boeretang 200, BR1 Building, B-2400 Mol (Belgium); Cinotti, Luciano [ANSALDO NUCLEARE, Divisione di ANSALDO ENERGIA SpA, Corso Perrone, 25, 16100 Genova (Italy); Giot, Michel [Universite Catholique de Louvain, 1, Place de l' Universite, B-1348 Louvain-la-Neuve (Belgium); Giraud, Benoit [Framatome ANP, 10 rue Juliette Recamier, 69456 Lyon Cedex 06 (France); Gonzalez, Enrique [CIEMAT, Avda Complutense 22 E-28040 Madrid (Spain); Granget, Gilbert; Pillon, Sylvie; Warin, Dominique [Commissariat a l' Energie Atomique, CEA, 31-33, rue de la Federation, 75752 Paris cedex (France); Monti, Stefano [ENEA FIS-NUC, Via Martiri di Monte Sole 4, I-40129 Bologna (Italy); Mueller, Alex C. [CNRS, 3, rue Michel-Ange, 75794 Paris cedex 16 (France); Salvatores, Massimo [Forschungszentrum Karlsruhe (FZK), Hermann-von-Helmholtz-Platz 1, 76344 Eggenstein-Lepoldshafen (Germany); Commissariat a l' Energie Atomique, CEA, 31-33, rue de la Federation, 75752 Paris cedex (France)

    2006-07-01

    The Integrated Project EUROTRANS (EURopean Research Programme for the Transmutation of High Level Nuclear Waste in an Accelerator Driven System) within the ongoing EURATOM 6. European Commission Framework Programme (FP6) is devoted to the study of transmutation of high-level waste from nuclear power plants. The work is focused on transmutation in an Accelerator Driven System (ADS). The objective of EUROTRANS is the design and the feasibility assessment of an industrial ADS prototype dedicated to transmutation. The necessary R and D results in the areas of fuel development, structural materials, thermal hydraulics, heavy liquid metal technology and nuclear data will be made available, together with the experimental demonstration of the ADS component coupling. The outcome of this work will allow to provide a reasonably reliable assessment of feasibility and a cost estimate for ADS based transmutation, and to possibly decide on the detailed design of an experimental ADS and its construction in the future. EUROTRANS will strengthen and consolidate the European research and development activities in transmutation. The involvement of universities strengthens education and training in nuclear technologies. The involvement of industries assures a market-oriented and economic design development and an effective dissemination of the results. The four-year project started in April 2005. (authors)

  9. Actinides(3)/lanthanides(3) separation by nano-filtration assisted by complexation; Separation actinides(3)lanthanides(3) par nanofiltration assistee par complexation

    Energy Technology Data Exchange (ETDEWEB)

    Sorin, A

    2006-07-01

    In France, one of the research trend concerning the reprocessing of spent nuclear fuel consists to separate selectively the very radio-toxic elements with a long life to be recycled (Pu) or transmuted (Am, Cm, Np). The aim of this thesis concerns the last theme about actinides(III)/lanthanides(III) separation by a process of nano-filtration assisted by complexation. Thus, a pilot of tangential membrane filtration was designed and established in a glove box at the ATALANTE place of CEA-Marcoule. Physico-chemical characterisation of the Desal GH membrane (OSMONICS), selected to carry out actinides(III)/lanthanides(III) separation, was realized to determine the zeta potential of the active layer and its resistance to ionizing radiations. Moreover, a parametric study was also carried out to optimize the selectivity of complexation, and the operating conditions of complex retention (influences of the transmembrane pressure, solute concentration, tangential velocity and temperature). Finally, the separation of traces of Am(III) contained in a mixture of lanthanides(III), simulating the real load coming from a reprocessing cycle, was evaluated with several chelating agents such as poly-amino-carboxylic acids according to the solution acidity and the [Ligand]/[Cation(III)] ratio. (author)

  10. RED-IMPACT. Impact of partitioning, transmutation and waste reduction technologies on the final nuclear waste disposal. Synthesis report

    Energy Technology Data Exchange (ETDEWEB)

    Lensa, Werner von; Nabbi, Rahim; Rossbach, Matthias (eds.) [Forschungszentrum Juelich GmbH (Germany)

    2008-07-01

    The impact of partitioning and transmutation (P and T) and waste reduction technologies on the nuclear waste management and particularly on the final disposal has been analysed within the EU-funded RED-IMPACT project. Five representative scenarios, ranging from direct disposal of the spent fuel to fully closed cycles (including minor actinide (MA) recycling) with fast neutron reactors or accelerator-driven systems (ADS), were chosen in the project to cover a wide range of representative waste streams, fuel cycle facilities and process performances. High and intermediate level waste streams have been evaluated for all of these scenarios with the aim of analysing the impact on geological disposal in different host formations such as granite, clay and salt. For each scenario and waste stream, specific waste package forms have been proposed and their main characteristics identified. Both equilibrium and transition analyses have been applied to those scenarios. The performed assessments have addressed parameters such as the total radioactive and radiotoxic inventory, discharges during reprocessing, thermal power and radiation emission of the waste packages, corrosion of matrices, transport of radioisotopes through the engineered and geological barriers or the resulting doses from the repository. The major conclusions of include the fact, that deep geological repository to host the remaining high level waste (HLW) and possibly the long-lived intermediate level waste (ILW) is unavoidable whatever procedure is implemented to manage waste streams from different fuel cycle scenarios including P and T of long-lived transuranic actinides.

  11. Selective Separation of Trivalent Actinides from Lanthanides by Aqueous Processing with Introduction of Soft Donor Atoms

    Energy Technology Data Exchange (ETDEWEB)

    Kenneth L. Nash; Sue B. Clark; Gregg Lumetta

    2009-09-23

    With increased application of MOX fuels and longer burnup times for conventional fuels, higher concentrations of the transplutonium actinides Am and Cm (and even heavier species like Bk and Cf) will be produced. The half-lives of the Am isotopes are significantly longer than those of the most important long-lived, high specific activity lanthanides or the most common Cm, Bk and Cf isotopes, thus the greatest concern as regards long-term radiotoxicity. With the removal and transmutation of Am isotopes, radiation levels of high level wastes are reduced to near uranium mineral levels within less than 1000 years as opposed to the time-fram if they remain in the wastes.

  12. LLNL SFA OBER SBR FY17 Program Management and Performance Report: Subsurface Biogeochemistry of Actinides

    Energy Technology Data Exchange (ETDEWEB)

    Kersting, Annie B. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States)

    2017-06-23

    A major scientific challenge in environmental sciences is to identify the dominant processes controlling actinide transport in the environment. It is estimated that currently, over 2200 metric tons of anthropogenic plutonium (Pu) has accumulated worldwide, a number that increases yearly with additional spent nuclear fuel (Ewing et al., 2010). Plutonium has been shown to migrate on the scale of kilometers, giving way to a critical concern that the fundamental biogeochemical processes that control its behavior in the subsurface are not well understood (Kersting et al. 1999; Novikov et al. 2006; Santschi et al. 2002). Neptunium (Np) is less prevalent in the environment; however, it is predicted to be a significant long-term dose contributor in high-level nuclear waste. Our focus on Np chemistry in this Science Plan is intended to help formulate a better understanding of Pu redox transformations in the environment and clarify the differences between the two long-lived actinides. The research approach of our Science Plan combines (1) Fundamental Mechanistic Studies that identify and quantify biogeochemical processes that control actinide behavior in solution and on solids, (2) Field Integration Studies that investigate the transport characteristics of Pu and test our conceptual understanding of actinide transport, and (3) Actinide Research Capabilities that allow us to achieve the objectives of this Scientific Focus Area (SFA) and provide new opportunities for advancing actinide environmental chemistry. These three Research Thrusts form the basis of our SFA Science Program.

  13. Enhancing the actinide sciences in Europe through hot laboratories networking and pooling: from ACTINET to TALISMAN

    Energy Technology Data Exchange (ETDEWEB)

    Bourg, S.; Poinssot, C. [French Nuclear and Alternative Energies Commission, CEA, Nuclear Energy Division, F RadioChemistry and Processes Department, CEA Marcoule, 30207 Bagnols sur Ceze (France)

    2013-07-01

    Since 2004, Europe supports the strengthening of the European actinides sciences scientific community through the funding of dedicated networks: (i) from 2004 to 2008, the ACTINET6 network of excellence (6. Framework Programme) gathered major laboratories involved in nuclear research and a wide range of academic research organisations and universities with the specific aims of funding and implementing joint research projects to be performed within the network of pooled facilities; (ii) from 2009 to 2013, the ACTINET-I3 integrated infrastructure initiative (I3) supports the cost of access of any academics in the pooled EU hot laboratories. In this continuation, TALISMAN (Trans-national Access to Large Infrastructures for a Safe Management of Actinides) gathers now the main European hot laboratories in actinides sciences in order to promote their opening to academics and universities and strengthen the EU-skills in actinides sciences. Furthermore, a specific focus is set on the development of advanced cutting-edge experimental and spectroscopic capabilities, the combination of state-of-the art experimental with theoretical first-principle methods on a quantum mechanical level and to benefit from the synergy between the different scientific and technical communities. ACTINET-I3 and TALISMAN attach a great importance and promote the Education and Training of the young generation of actinides scientists in the Trans-national access but also by organizing Schools (general Summer Schools or Theoretical User Lab Schools) or by granting students to attend International Conference on actinide sciences. (authors)

  14. Accelerator-driven transmutation technologies for resolution of long-term nuclear waste concerns

    Energy Technology Data Exchange (ETDEWEB)

    Bowman, C.D.

    1996-10-01

    The paper provides a rationale for resolution of the long-term waste disposition issue based on complete destruction of fissile material and all higher actinides. It begins with a brief history of geologic storage leading to the present impasse in the US. The proliferation aspects of commercial plutonium are presented in a new light as a further driver for complete destruction. The special problems in Russia and the US of the disposition of the highly enriched spent naval reactor fuel and spent research reactor fuel are also presented. The scale of the system required for complete destruction is also examined and it is shown that a practical system for complete destruction of commercial and defense fissile material must be widely dispersed rather than concentrated at a single site. Central tenants of the US National Academy of Sciences recommendations on waste disposition are examined critically and several technologies considered for waste destruction are described briefly and compared Recommendations for waste disposition based on Accelerator-Driven Transmutation Technology suitable for both the US and Russia are presented.

  15. Preliminary studies of a new accelerator-driven minor actinide burner in industrial scale

    Energy Technology Data Exchange (ETDEWEB)

    Li, Xunzhao; Zhou, Shengcheng [School of Nuclear Science and Technology, Xi’an Jiaotong University, Xi’an 710049, Shaanxi (China); Zheng, Youqi, E-mail: yqzheng@mail.xjtu.edu.cn [School of Nuclear Science and Technology, Xi’an Jiaotong University, Xi’an 710049, Shaanxi (China); Wang, Kunpeng [Nuclear and Radiation Safety Center, PO Box 8088, No. 54, Beijing 100082 (China); Wu, Hongchun [School of Nuclear Science and Technology, Xi’an Jiaotong University, Xi’an 710049, Shaanxi (China)

    2015-10-15

    Highlights: • A new accelerator-driven minor actinide (MA) burner was proposed. • Comprehensive design of spallation target, fuel assembly and subcritical core was performed. • Preliminary safety analyses indicate the inherent safety of the core in the reactivity insertion (500 pcm) and beam overpower (50% increase) transients. - Abstract: Pursuing high transmutation rate of minor actinide (MA), a preliminary conceptual design of a lead-bismuth (LBE) cooled accelerator-driven system (ADS) is proposed in this study. Parametric studies are performed to optimize the neutronics and thermal–hydraulics performances. The proton energy and axial position of the proton beam impact is investigated to obtain high neutron source efficiency and spallation neutron yield. The influences of MA/Pu mixing ratio and the ratio of pin pitch to diameter (P/D) are also optimized to control the burnup reactivity swing and the minimum coolant velocity for adequate cooling. To reduce the power peak, three kinds of power flattening techniques are adopted and compared. The results show that the inert matrix ratio zone loading method seems more versatile. Based on the analyses, an optimized three zone loading pattern is proposed for the 800 MWth subcritical core. The total transmutation rate of MA is 328.8 kg per effective full power year. Preliminary safety analyses based on the balance of power method (BOP) are performed and the results show that in the reactivity insertion and beam overpower transients, the core shows inherent safety, but the scram is necessary by cutting off the beam current to protect the core from possible damages caused by the loss of flow.

  16. Current Status of the Transmutation Reactor Technology and Preliminary Evaluation of Transmutation Performance of the KALIMER Core

    Energy Technology Data Exchange (ETDEWEB)

    Hong, Ser Gi; Sim, Yoon Sub; Kim, Yeong Il; Kim, Young Gyum; Lee, Byung Woon; Song, Hoon; Lee, Ki Bog; Jang, Jin Wook; Lee, Dong Uk

    2005-08-15

    Recently the most countries using the nuclear power plants for electricity generation have been faced with the problem of the preparation of the repository for the disposition of the nuclear waste generated from LWR. It was well-known that the issues related with long term risk of the radioactive wastes for the future generations are due only to 1% of the total waste. This small fraction of 1% consists of transuranic (TRU) nuclides such as Pu, Np, Am, Cm and the long lived fission products such as Tc and I. For the transuranic (TRU) nuclides, their half lives range from several years to several hundred thousands years and hence their radioactive toxicity can be lasted over very long time period. This has made the change of the rule of the fast spectrum reactor from the economical use of uranium resource through breeding to the reduction of the nuclear waste through the transmutation. The purpose of this study is to obtain the basic knowledge on the nuclear transmutation technology and to suggest the technical solution ways for the future technology development and enhancement through a survey of the state-of-art of the international research on the nuclear transmutation. The increase of the transmutation rate requires the reduction of the breeding ratio. In fact, the transmutation rate is determined by the breeding ratio. The reduction of the breeding ratio can be achieved by reducing the U-238 content in fuel or increasing the neutron leakage through core boundary or absorbing the neutrons by using some absorbers. However, the reduction of the U-238 content results in the degradation of the fuel Doppler coefficient that is one of the most important safety-related parameters and the reduction of the effective delayed neutron fraction that is related with the controllability of the reactor core. Also, the increase of the transmutation rate can lead to the increase of the coolant void reactivity worth unless some ways to reduce the coolant void reactivity are not

  17. Partitioning and transmutation. Current developments - 2010. A report from the Swedish reference group for PT-research

    Energy Technology Data Exchange (ETDEWEB)

    Blomgren, Jan (ed.) (Swedish Centre for Nuclear Technology, SKC, Stockholm (Sweden)); Karlsson, Fred (Swedish Nuclear Fuel and Waste Management Co., Stockholm (Sweden)); Pomp, Stephan (Uppsala Univ., Uppsala, Dept. of Physics and Astronomy, Div. of Applied Nuclear Physics (Sweden)); Aneheim, Emma; Ekberg, Christian; Fermvik, Anna; Skarnemark, Gunnar (Nuclear Chemistry, Dept. of Chemical and Biological Engineering, Chalmers Univ. of Technology, Goeteborg (Sweden)); Wallenius, Janne; Zakova, Jitka (Reactor Physics Div., Physics Dept., Royal Inst. of Technology, Stockholm (Sweden)); Grenthe, Ingemar; Szabo, Zoltan (School of Chemical Science and Engineering, Royal Inst. of Technology, Stockholm (Sweden))

    2010-01-15

    The research and development on methods for partitioning and transmutation (P and T) of long-lived radionuclides in spent nuclear fuel has attracted considerable interest during the last decade. The main objective of P and T is to eliminate or at least substantially reduce the amount of such long-lived radionuclides that has to go to a deep geological repository for final disposal. The objective of current research on partitioning is to find and develop processes suitable for separation of the heavier actinides (and possibly some long-lived fission products) on an industrial scale. The objective of current research on transmutation is to define, investigate and develop facilities that may be suitable for transmutation of the long-lived radionuclides. The research on partitioning has made important progress in recent years. In some cases one has succeeded to separate americium and curium. Many challenges remain however. Within hydrochemistry one has achieved sufficiently good distribution and separation factors. The focus turns now towards development of an operating process. The search for ligands that give sufficiently good extraction and separation will continue but with less intensity. The emphasis will rather be on improving stability against hydrolysis and radiolysis. This may be achieved either by additives to the solvent or by selection of a proper solvent. The development of processes and equipment must be intensified. Pyrochemical research is looking into methods for recovery of uranium and for separating fission products with large neutron cross sections. The objective is to avoid separation of plutonium from other transuranium elements and thus simplify the proliferation issue. The future work is focused on improved selectivity and on technical development. Design of processes and equipment is difficult due to the aggressive properties of the melts and the relatively high temperatures required. The fabrication of fuel for transmutation and the

  18. Criticality investigations for the fixed bed nuclear reactor using thorium fuel mixed with plutonium or minor actinides

    Energy Technology Data Exchange (ETDEWEB)

    Sahin, Suemer [Beykoz Lojistik Meslek Yueksekokulu, Beykoz, Istanbul (Turkey)], E-mail: sumer@gazi.edu.tr; Sahin, Haci Mehmet; Acir, Adem [Beykoz Lojistik Meslek Yueksekokulu, Istanbul (Turkey); Al-Kusayer, Tawfik Ahmed [King Saud University, College of Engineering, P.O. Box 800, Riyadh 11421 (Saudi Arabia)

    2009-08-15

    Prospective fuels for a new reactor type, the so called fixed bed nuclear reactor (FBNR) are investigated with respect to reactor criticality. These are (1) low enriched uranium (LEU); (2) weapon grade plutonium + ThO{sub 2}; (3) reactor grade plutonium + ThO{sub 2}; and (4) minor actinides in the spent fuel of light water reactors (LWRs) + ThO{sub 2}. Reactor grade plutonium and minor actinides are considered as highly radio-active and radio-toxic nuclear waste products so that one can expect that they will have negative fuel costs. The criticality calculations are conducted with SCALE5.1 using S{sub 8}-P{sub 3} approximation in 238 neutron energy groups with 90 groups in thermal energy region. The study has shown that the reactor criticality has lower values with uranium fuel and increases passing to minor actinides, reactor grade plutonium and weapon grade plutonium. Using LEU, an enrichment grade of 9% has resulted with k{sub eff} = 1.2744. Mixed fuel with weapon grade plutonium made of 20% PuO{sub 2} + 80% ThO{sub 2} yields k{sub eff} = 1.2864. Whereas a mixed fuel with reactor grade plutonium made of 35% PuO{sub 2} + 65% ThO{sub 2} brings it to k{sub eff} = 1.267. Even the very hazardous nuclear waste of LWRs, namely minor actinides turn out to be high quality nuclear fuel due to the excellent neutron economy of FBNR. A relatively high reactor criticality of k{sub eff} = 1.2673 is achieved by 50% MAO{sub 2} + 50% ThO{sub 2}. The hazardous actinide nuclear waste products can be transmuted and utilized as fuel in situ. A further output of the study is the possibility of using thorium as breeding material in combination with these new alternative fuels.

  19. Prompt fission neutron spectrum of actinides

    Energy Technology Data Exchange (ETDEWEB)

    Capote, R. [International Atomic Energy Agency, Vienna (Austria); Chen, Y. -J. [China Institute of Atomic Energy, Beijing (China); Hambsch, F. J. [European Commission, Joint Research Centre - IRRM, Geel (Belgium); Jurado, B. [CENBG, CNRS/IN2P3, Gradignan (France); Kornilov, N. [Ohio Univ., Athens, OH (United States); Lestone, J. P. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Litaize, O. [CEA, DEN, DER, SPRC, Saint-Paul-Lez-Durance (France); Morillon, B. [CEA, DAM, DIF, Arpajon (France); Neudecker, D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Oberstedt, S. [European Commission, Joint Research Centre - IRRM, Geel (Belgium); Ohsawa, T. [Kinki Univ., Osaka-fu (Japan); Otuka, N. [International Atomic Energy Agency, Vienna (Austria); Pronyaev, V. G. [Institute of Physics and Power Engineering, Obninsk (Russian Federation); Saxena, A. [Bhabha Atomic Research Centre, Mumbai (India); Schmidt, K. H. [CENBG, CNRS/IN2P3, Gradignan (France); Serot, O. [CEA, DEN, DER, SPRC, Saint-Paul-Lez-Durance (France); Shcherbakov, O. A. [Petersburg Nuclear Physics Institute of NRC " Kurchatov Institute" , Gatchina (Russian Federation); Shu, N. -C. [China Institute of Atomic Energy, Beijing (China); Smith, D. L. [Argonne National Lab. (ANL), Argonne, IL (United States); Talou, P. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Trkov, A. [International Atomic Energy Agency, Vienna (Austria); Tudora, A. C. [Univ. of Bucharest, Magurele (Romania); Vogt, R. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Univ. of California, Davis, CA (United States); Vorobyev, A. S. [Petersburg Nuclear Physics Institute of NRC " Kurchatov Institute" , Gatchina (Russian Federation)

    2016-01-06

    Here, the energy spectrum of prompt neutron emitted in fission (PFNS) plays a very important role in nuclear science and technology. A Coordinated Research Project (CRP) "Evaluation of Prompt Fission Neutron Spectra of Actinides" was established by the IAEA Nuclear Data Section in 2009, with the major goal to produce new PFNS evaluations with uncertainties for actinide nuclei.

  20. Calculated Atomic Volumes of the Actinide Metals

    DEFF Research Database (Denmark)

    Skriver, H.; Andersen, O. K.; Johansson, B.

    1979-01-01

    The equilibrium atomic volume is calculated for the actinide metals. It is possible to account for the localization of the 5f electrons taking place in americium.......The equilibrium atomic volume is calculated for the actinide metals. It is possible to account for the localization of the 5f electrons taking place in americium....

  1. Catalytic Organic Transformations Mediated by Actinide Complexes

    Directory of Open Access Journals (Sweden)

    Isabell S. R. Karmel

    2015-10-01

    Full Text Available This review article presents the development of organoactinides and actinide coordination complexes as catalysts for homogeneous organic transformations. This chapter introduces the basic principles of actinide catalysis and deals with the historic development of actinide complexes in catalytic processes. The application of organoactinides in homogeneous catalysis is exemplified in the hydroelementation reactions, such as the hydroamination, hydrosilylation, hydroalkoxylation and hydrothiolation of alkynes. Additionally, the use of actinide coordination complexes for the catalytic polymerization of α-olefins and the ring opening polymerization of cyclic esters is presented. The last part of this review article highlights novel catalytic transformations mediated by actinide compounds and gives an outlook to the further potential of this field.

  2. Actinide ion sensor for pyroprocess monitoring

    Science.gov (United States)

    Jue, Jan-fong; Li, Shelly X.

    2014-06-03

    An apparatus for real-time, in-situ monitoring of actinide ion concentrations which comprises a working electrode, a reference electrode, a container, a working electrolyte, a separator, a reference electrolyte, and a voltmeter. The container holds the working electrolyte. The voltmeter is electrically connected to the working electrode and the reference electrode and measures the voltage between those electrodes. The working electrode contacts the working electrolyte. The working electrolyte comprises an actinide ion of interest. The reference electrode contacts the reference electrolyte. The reference electrolyte is separated from the working electrolyte by the separator. The separator contacts both the working electrolyte and the reference electrolyte. The separator is ionically conductive to the actinide ion of interest. The reference electrolyte comprises a known concentration of the actinide ion of interest. The separator comprises a beta double prime alumina exchanged with the actinide ion of interest.

  3. Transmutation of sup 2 sup 0 sup 4 Pb in an intensive gamma-ray flux

    CERN Document Server

    Ishkhanov, B S

    2001-01-01

    Transmutation chain formation during irradiation with various intensities of bremsstrahlung photon beam is analysed. The main features of transmutation chain formation by photons with energies corresponding to the giant dipole resonance are discussed.

  4. Neutron dynamics of fast-spectrum dedicated cores for waste transmutation; Etude et amelioration du comportement cinetique de coeurs rapides a la transmutation de dechets a vie longue

    Energy Technology Data Exchange (ETDEWEB)

    Massara, S

    2002-04-01

    Among different scenarios achieving minor actinide transmutation, the possibility of double strata scenarios with critical, fast spectrum, dedicated cores must be checked and quantified. In these cores, the waste fraction has to be at the highest level compatible with safety requirements during normal operation and transient conditions. As reactivity coefficients are poor in such critical cores (low delayed neutron fraction and Doppler feed-back, high coolant void coefficient), their dynamic behaviour during transient conditions must be carefully analysed. Three nitride-fuel configurations have been analysed: two liquid metal-cooled (sodium and lead) and a particle-fuel helium-cooled one. A dynamic code, MAT4 DYN, has been developed during the PhD thesis, allowing the study of loss of flow, reactivity insertion and loss of coolant accidents, and taking into account two fuel geometries (cylindrical and spherical) and two thermal-hydraulics models for the coolant (incompressible for liquid metals and compressible for helium). Dynamics calculations have shown that if the fuel nature is appropriately chosen (letting a sufficient margin during transients), this can counterbalance the bad state of reactivity coefficients for liquid metal-cooled cores, thus proving the interest of this kind of concept. On the other side, the gas-cooled core dynamics is very badly affected by the high value of the helium void coefficient (which is a consequence of the choice of a hard spectrum), this effect being amplified by the very low thermal inertia of particle-fuel design. So, a new kind of concept should be considered for a helium-cooled fast-spectrum dedicated core. (authors)

  5. Ionic Interactions in Actinide Tetrahalides

    Science.gov (United States)

    Akdeniz, Z.; Karaman, A.; Tosi, M. P.

    2001-05-01

    We determine a model of the ionic interactions in AX 4 compounds (where A is an atom in the actinide series from Th to Am and X = F, Cl, Br or I) by an analysis of data on the static and dynamic structure of their molecular monomers. The potential energy function that we adopt is taken from earlier work on rare-earth trihalides [Z. Akdeniz, Z. Q q e k and M. P. Tosi, Z. Naturforsch. 55a, 861 (2000)] and in particular allows for the electronic polarizability of the actinide ion. This polarizability quantitatively determines the antisymmetric-bending vibrational mode, but its magnitude remains compatible with a symmetric tetrahedral shape of the molecule at equilibrium. The fluorides have an especially high degree of ionic character, and the interionic-force parameters for each halide of the U, Np, Pu and Am series show regular trends, suggesting that extrapolations to the other transuranic-element halides may usefully be made. The Th compounds show some deviations from these trends, and the interionic-force model that we determine for ThCl4 differs somewhat from that obtained in a previous study. We therefore return on the evaluation of the relative stability of charged oligomers of ThCl4 and ZrCl4 and find confirmation of our earlier results on this problem.

  6. PKA distributions: Contributions from transmutation products and from radioactive decay

    Directory of Open Access Journals (Sweden)

    M.R. Gilbert

    2016-12-01

    Full Text Available The neutrons generated in fusion plasmas interact with materials via nuclear reactions. The resulting transmutations and atomic displacements have life-limiting consequences for fusion reactor components. A detailed understanding of the production, evolution and material consequences of the damage created by cascades of atomic displacements requires, as a vital primary input, a complete description of the energy-spectrum of initial (prompt atomic displacement events (the primary knock on atoms or PKAs produced by direct neutron nuclear interactions. There is also the possibility that the radionuclides produced under transmutation will create further PKAs as they decay, and so the rate of these must also be quantified. This paper presents the latest results from the analysis of PKA spectra under neutron irradiation, focussing particularly on the variation in PKA distributions due to changes in composition under transmutation, but also on the PKA contributions from radioactive decay of materials that become activated under irradiation.

  7. Resolving and quantifying overlapped chromatographic bands by transmutation

    Science.gov (United States)

    Malinowski

    2000-09-15

    A new chemometric technique called "transmutation" is developed for the purpose of sharpening overlapped chromatographic bands in order to quantify the components. The "transmutation function" is created from the chromatogram of the pure component of interest, obtained from the same instrument, operating under the same experimental conditions used to record the unresolved chromatogram of the sample mixture. The method is used to quantify mixtures containing toluene, ethylbenzene, m-xylene, naphthalene, and biphenyl from unresolved chromatograms previously reported. The results are compared to those obtained using window factor analysis, rank annihilation factor analysis, and matrix regression analysis. Unlike the latter methods, the transmutation method is not restricted to two-dimensional arrays of data, such as those obtained from HPLC/DAD, but is also applicable to chromatograms obtained from single detector experiments. Limitations of the method are discussed.

  8. A prospective fuel cycle for long lived radionuclide transmutation

    Energy Technology Data Exchange (ETDEWEB)

    Yoo, Jae Hyung; Shim, Joon Bo; Ahn, Byung Gil [Korea Atomic Energy Research Institute, Taejon (Korea, Republic of)

    1999-07-01

    This study is aimed at outlining a prospective fuel cycle applicable to the nuclear transmutation of long lived radionuclides. Recycling the uranium and plutonium of spent fuels by Purex reprocessing is known to be far from an economical way at present. In addition, it generates high-level rad waste containing long-lived radionuclides, which would be a great burden to the subsequent final disposal in terms of cost, safety, and risks of environmental impact. As an alternative way to overcome this problem while still recycling the valuable fissionable materials as energy resources, transmutation is being taken into account by scientists in many countries. The concept of P{center_dot}T cycle suggested in this study is based on the technological requirements in relation with the transmutation system, while lowering the burden of waste disposal as well as risks of nuclear proliferation. (author)

  9. On the Transmutability of Textual Data: Concept and Practices

    Directory of Open Access Journals (Sweden)

    Catarina Lee

    2016-11-01

    Full Text Available This paper discusses the creative potential of the transmutability of digital data, while focusing on the exploration of textual material. It begins by addressing the conceptual and creative possibilities associated to the topic, and then discusses artifacts that imply or express transmutability as an artistic concept and method. To this end, we resort to a framework for the description and analysis of these artifacts, focusing on their conceptual dimension, on their mechanics and on the elements of their experience. In particular, we address the concepts they approach through the use of data in textual formats as source information or content, we consider the processes for its manipulation, and describe the resulting sensory manifestations while emphasizing their dynamics and variability. In this manner, this study seeks to highlight how transmutability becomes relevant as an artistic argument, by proposing aesthetic experiences that explore the ubiquity and heterogeneity of data in our contemporary world, as it becomes available in text formats.

  10. MA Doping Analysis on Breeding Capability and Protected Plutonium Production of Large FBR

    Science.gov (United States)

    Permana, Sidik; Suzuki, Mitsutoshi; Kuno, Yusuke

    2010-06-01

    Spent fuel from LWR can be seen as long-live waste if it is not recycled or as a "new fuel" resource if it is recycled into the reactors. Uranium and plutonium have been used for "new fuel" resources from LWR spent fuel as MOX fuel type which is loaded into thermal reactor or fast reactor types. Other actinides from the spent fuel such as neptunium, americium and curium as minor actinide (MA) are considered to be loaded into the reactors for specific purposes, recently. Those purposes such as for increasing protected plutonium production and breeding capability for protected plutonium as well as in the same time those amount of MA can be reduced to a small quantity as a burner or transmutation purpose. Some investigations and scientific approaches are performed in order to increase a material "barrier" in plutonium isotope composition by increasing the even mass number of plutonium isotope such as Pu-238, Pu-240 and Pu-242 as plutonium protected composition. Higher material barrier which related to intrinsic properties of plutonium isotopes with even mass number (Pu-238, Pu-240 and Pu-242), are recognized because of their intense decay heat (DH) and high spontaneous fission neutron (SFN) rates. Those even number mass of plutonium isotope contribute to some criteria of plutonium characterization which will be adopted for present study such as IAEA, Pellaud and Kessler criteria (IAEA, 1972; Pellaud, 2002; and Kessler, 2007). The present paper intends to evaluate the breeding capability as a fuel sustainability index of the reactors and to analyze the composition of protected plutonium production of large power reactor based on the FaCT FBR as reference (Ohki, et al., 2008). Three dimensional FBR core configuration has been adopted which is based on the core optimization calculation of SRAC-CITATION code as reactor core analysis and JENDL-3.3 is adopted for nuclear data library. Some MA doping materials are loaded into the blanket regions which can be considered as

  11. Nickel Foil as Transmutation Detector for Neutron Fluence Measurements

    Science.gov (United States)

    Klupák, Vít; Viererbl, Ladislav; Lahodová, Zdena; Šoltés, Jaroslav; Tomandl, Ivo; Kudějová, Petra

    2016-02-01

    Activation detectors are very often used for determination of the neutron fluence in reactor dosimetry. However, there are few disadvantages concerning these detectors; it is the demand of the knowledge of the irradiation history and a loss of information due to a radioactive decay in time. Transmutation detectors TMD could be a solution in this case. The transmutation detectors are materials in which stable or long-lived nuclides are produced by nuclear reactions with neutrons. From a measurement of concentration of these nuclides, neutron fluence can be evaluated regardless of the cooling time.

  12. Nickel Foil as Transmutation Detector for Neutron Fluence Measurements

    Directory of Open Access Journals (Sweden)

    Klupák Vít

    2016-01-01

    Full Text Available Activation detectors are very often used for determination of the neutron fluence in reactor dosimetry. However, there are few disadvantages concerning these detectors; it is the demand of the knowledge of the irradiation history and a loss of information due to a radioactive decay in time. Transmutation detectors TMD could be a solution in this case. The transmutation detectors are materials in which stable or long-lived nuclides are produced by nuclear reactions with neutrons. From a measurement of concentration of these nuclides, neutron fluence can be evaluated regardless of the cooling time.

  13. Electron trap annealing in neutron transmutation doped silicon

    DEFF Research Database (Denmark)

    Guldberg, J.

    1977-01-01

    Silicon doped by neutron transmutation to 1.2×1014 phosphorus atoms/cm3 was investigated with deep level transient spectroscopy using evaporated Au/n-Si diodes. Seven bulk electron traps were identified which appear after 30 min N2 anneal at temperatures between 425 and 725 °C. Five of these anne......Silicon doped by neutron transmutation to 1.2×1014 phosphorus atoms/cm3 was investigated with deep level transient spectroscopy using evaporated Au/n-Si diodes. Seven bulk electron traps were identified which appear after 30 min N2 anneal at temperatures between 425 and 725 °C. Five...

  14. Impact of transmutations in fusion environment on Flibe chemistry.

    Energy Technology Data Exchange (ETDEWEB)

    Sze, D. K.; Sawan, M. E.; Cheng, E. T.

    2000-11-15

    Transmutation rates of Li, Be and F are calculated for a typical flibe blanket. The results concluded that the transmutation rate of F is more than double that of Be. Because of the high destruction rate of fluorine, there will be no free fluorine in the molten salt. Therefore, experimental program to address the chemistry control of flibe does not have to worry about the issues associated with free fluorine. Also, this calculation defines the chemical of flibe after irradiation. This chemical state needs to be simulated closely for the flibe chemistry control experiment.

  15. Spin and orbital moments in actinide compounds

    DEFF Research Database (Denmark)

    Lebech, B.; Wulff, M.; Lander, G.H.

    1991-01-01

    experiments designed to determine the magnetic moments at the actinide and transition-metal sublattice sites in compounds such as UFe2, NpCo2, and PuFe2 and to separate the spin and orbital components at the actinide sites. The results show, indeed, that the ratio of the orbital to spin moment is reduced......The extended spatial distribution of both the transition-metal 3d electrons and the actinide 5f electrons results in a strong interaction between these electron states when the relevant elements are alloyed. A particular interesting feature of this hybridization, which is predicted by single...

  16. Experimental studies of actinides in molten salts

    Energy Technology Data Exchange (ETDEWEB)

    Reavis, J.G.

    1985-06-01

    This review stresses techniques used in studies of molten salts containing multigram amounts of actinides exhibiting intense alpha activity but little or no penetrating gamma radiation. The preponderance of studies have used halides because oxygen-containing actinide compounds (other than oxides) are generally unstable at high temperatures. Topics discussed here include special enclosures, materials problems, preparation and purification of actinide elements and compounds, and measurements of various properties of the molten volts. Property measurements discussed are phase relationships, vapor pressure, density, viscosity, absorption spectra, electromotive force, and conductance. 188 refs., 17 figs., 6 tabs.

  17. Recovery of actinides from actinide-aluminium alloys by chlorination: Part I

    OpenAIRE

    Cassayre, Laurent; Soucek, Pavel; Mendes, Eric; Malmbeck, Rikard; Nourry, Christophe; Eloirdi, Rachel; Glatz, Jean-Paul

    2011-01-01

    Pyrochemical processes in molten LiCl–KCl are being developed in ITU for recovery of actinides from spent nuclear fuel. The fuel is anodically dissolved to the molten salt electrolyte and actinides are electrochemically reduced on solid aluminium cathodes forming solid actinide–aluminium alloys. A chlorination route is being investigated for recovery of actinides from the alloys. This route consists in three steps: Vacuum distillation for removal of the salt adhered on the electrode, chlorina...

  18. The transmutation of americium: the Ecrix experiments in Phenix; Transmutation de l'americium: les experiences ecrix dans Phenix

    Energy Technology Data Exchange (ETDEWEB)

    Garnier, J.C.; Schmidt, N. [CEA Cadarache, Dept. d' Etudes des Combustibles (DEC/SESC), 13 - Saint-Paul-lez-Durance (France); Croixmarie, Y.; Ottaviani, J.P. [CEA Cadarache, Dept. d' Etudes des Combustibles (DEC/SPUA), 13 - Saint-Paul-lez-Durance (France); Varaine, F.; Saint Jean, C. de [CEA Cadarache, Dept. d' Etudes des Reacteurs (DER/SPRC), 13 - Saint-Paul-lez-Durance (France)

    1999-07-01

    The first americium transmutation experiment in a specific target in PHENIX will occur with the ECRIX-B and ECRIX-H experiments. Beside material testing, the objective is also to represent a concept of transmutation whose specificity is to enhance the kinetics of transmutation by using a moderated spectrum. The moderator materials will be {sup 11}B{sub 4}C and CaH{sub 2} for ECRIX-B and ECRIXH respectively, the irradiation conditions have been predicted for both the neutronics and thermal. The targets (MgO-AmO{sub X} pellets) are manufactured in the ATALANTE laboratory and the design is performed according to the PHENIX operating conditions. (authors)

  19. {sup 99}Tc transmutation by spallation neutrons produced in a large lead block; Transmutation de {sup 99}Tc par des neutrons de spallation produits dans un grand massif de plomb

    Energy Technology Data Exchange (ETDEWEB)

    Andriamonje, S.; Arnould, H.; Bompas, C.A.; Del Moral, R.; Lacoste, V. [Centre d`Etudes Nucleaires, Bordeaux-1 Univ., 33 Gradignan (France); TARC Collaboration under leadership of C. Rubbia

    1997-06-01

    In the search of hybrid system (the coupling of the particle accelerator to an under-critical reactor) for radioactive waste transmutation the TARC (Transmutation by Adiabatic Resonance Crossing) program has been developed. One of the target of the TARC program is the study of the efficiency of a `Energy Amplifier` system for nuclear waste incineration. Among the radioactive wastes the most interesting is the fission product {sup 99}Tc from nuclear plants heaving a half-live of {approx} 10{sup 5} years. Using a fast rabbit technique and gamma ray spectroscopy, the transmutation rate of {sup 99}Tc by spallation neutrons inside a large lead block was measured. The data from each 9 s rabbit cycle were stocked by means of an acquisition system based on the CERN CASCADE code especially adapted for gamma spectroscopy and able to catch large amounts of coincidence events. The measurements technique is described and the preliminary results are given. Also, in progress are simulations using new technique for production and propagation of neutrons in lead. Due to the plenty of spallation neutrons the capability of burning certain nuclear wastes is already proved

  20. Subsurface interactions of actinide species and microorganisms : implications for the bioremediation of actinide-organic mixtures.

    Energy Technology Data Exchange (ETDEWEB)

    Banaszak, J.E.; Reed, D.T.; Rittmann, B.E.

    1999-02-12

    By reviewing how microorganisms interact with actinides in subsurface environments, we assess how bioremediation controls the fate of actinides. Actinides often are co-contaminants with strong organic chelators, chlorinated solvents, and fuel hydrocarbons. Bioremediation can immobilize the actinides, biodegrade the co-contaminants, or both. Actinides at the IV oxidation state are the least soluble, and microorganisms accelerate precipitation by altering the actinide's oxidation state or its speciation. We describe how microorganisms directly oxidize or reduce actinides and how microbiological reactions that biodegrade strong organic chelators, alter the pH, and consume or produce precipitating anions strongly affect actinide speciation and, therefore, mobility. We explain why inhibition caused by chemical or radiolytic toxicities uniquely affects microbial reactions. Due to the complex interactions of the microbiological and chemical phenomena, mathematical modeling is an essential tool for research on and application of bioremediation involving co-contamination with actinides. We describe the development of mathematical models that link microbiological and geochemical reactions. Throughout, we identify the key research needs.

  1. BWR Assembly Optimization for Minor Actinide Recycling

    Energy Technology Data Exchange (ETDEWEB)

    G. Ivan Maldonado; John M. Christenson; J.P. Renier; T.F. Marcille; J. Casal

    2010-03-22

    The Primary objective of the proposed project is to apply and extend the latest advancements in LWR fuel management optimization to the design of advanced boiling water reactor (BWR) fuel assemblies specifically for the recycling of minor actinides (MAs).

  2. Advanced Aqueous Separation Systems for Actinide Partitioning

    Energy Technology Data Exchange (ETDEWEB)

    Nash, Kenneth L.; Clark, Sue; Meier, G Patrick; Alexandratos, Spiro; Paine, Robert; Hancock, Robert; Ensor, Dale

    2012-03-21

    One of the most challenging aspects of advanced processing of spent nuclear fuel is the need to isolate transuranium elements from fission product lanthanides. This project expanded the scope of earlier investigations of americium (Am) partitioning from the lanthanides with the synthesis of new separations materials and a centralized focus on radiochemical characterization of the separation systems that could be developed based on these new materials. The primary objective of this program was to explore alternative materials for actinide separations and to link the design of new reagents for actinide separations to characterizations based on actinide chemistry. In the predominant trivalent oxidation state, the chemistry of lanthanides overlaps substantially with that of the trivalent actinides and their mutual separation is quite challenging.

  3. Overview of actinide chemistry in the WIPP

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-01-01

    The year 2009 celebrates 10 years of safe operations at the Waste Isolation Pilot Plant (WIPP), the only nuclear waste repository designated to dispose defense-related transuranic (TRU) waste in the United States. Many elements contributed to the success of this one-of-the-kind facility. One of the most important of these is the chemistry of the actinides under WIPP repository conditions. A reliable understanding of the potential release of actinides from the site to the accessible environment is important to the WIPP performance assessment (PA). The environmental chemistry of the major actinides disposed at the WIPP continues to be investigated as part of the ongoing recertification efforts of the WIPP project. This presentation provides an overview of the actinide chemistry for the WIPP repository conditions. The WIPP is a salt-based repository; therefore, the inflow of brine into the repository is minimized, due to the natural tendency of excavated salt to re-seal. Reducing anoxic conditions are expected in WIPP because of microbial activity and metal corrosion processes that consume the oxygen initially present. Should brine be introduced through an intrusion scenario, these same processes will re-establish reducing conditions. In the case of an intrusion scenario involving brine, the solubilization of actinides in brine is considered as a potential source of release to the accessible environment. The following key factors establish the concentrations of dissolved actinides under subsurface conditions: (1) Redox chemistry - The solubility of reduced actinides (III and IV oxidation states) is known to be significantly lower than the oxidized forms (V and/or VI oxidation states). In this context, the reducing conditions in the WIPP and the strong coupling of the chemistry for reduced metals and microbiological processes with actinides are important. (2) Complexation - For the anoxic, reducing and mildly basic brine systems in the WIPP, the most important

  4. Layer thickness evaluation for transuranic transmutation in a fusion–fission system

    Energy Technology Data Exchange (ETDEWEB)

    Velasquez, Carlos E., E-mail: carlosvelcab@eng-nucl.mest.ufmg.br [Departamento de Engenharia Nuclear—Universidade Federal de Minas Gerais, Av. Antonio Carlos, 6627 Campus UFMG, 31.270-90, Belo Horizonte, MG (Brazil); Instituto Nacional de Ciência e Tecnologia de Reatores Nucleares Inovadores/CNPq, Rio de Janeiro, RJ (Brazil); Rede Nacional de Fusão (FINEP/CNPq), Rio de Janeiro, RJ (Brazil); Pereira, Claubia, E-mail: claubia@nuclear.ufmg.br [Departamento de Engenharia Nuclear—Universidade Federal de Minas Gerais, Av. Antonio Carlos, 6627 Campus UFMG, 31.270-90, Belo Horizonte, MG (Brazil); Instituto Nacional de Ciência e Tecnologia de Reatores Nucleares Inovadores/CNPq, Rio de Janeiro, RJ (Brazil); Rede Nacional de Fusão (FINEP/CNPq), Rio de Janeiro, RJ (Brazil); Veloso, Maria Auxiliadora F., E-mail: dora@nuclear.ufmg.br [Departamento de Engenharia Nuclear—Universidade Federal de Minas Gerais, Av. Antonio Carlos, 6627 Campus UFMG, 31.270-90, Belo Horizonte, MG (Brazil); Instituto Nacional de Ciência e Tecnologia de Reatores Nucleares Inovadores/CNPq, Rio de Janeiro, RJ (Brazil); Rede Nacional de Fusão (FINEP/CNPq), Rio de Janeiro, RJ (Brazil); Costa, Antonella L., E-mail: antonella@nuclear.ufmg.br [Departamento de Engenharia Nuclear—Universidade Federal de Minas Gerais, Av. Antonio Carlos, 6627 Campus UFMG, 31.270-90, Belo Horizonte, MG (Brazil); Instituto Nacional de Ciência e Tecnologia de Reatores Nucleares Inovadores/CNPq, Rio de Janeiro, RJ (Brazil); Rede Nacional de Fusão (FINEP/CNPq), Rio de Janeiro, RJ (Brazil)

    2015-05-15

    Highlights: • Layer thickness for transmutation in a fusion–fission system was evaluated. • The calculations were performed using MONTEBURNS code. • The results indicate the best thickness and volume ratio to induce transmutation. - Abstract: Layer thickness for transuranic transmutation in a fusion–fission system was evaluated using two different ways. In the first one, transmutation layer thicknesses were designed maintaining the fuel rod radius constant; in the second part, while the transmutation layer thickness increases, the fuel rod radius decreases maintaining k{sub s} (source-multiplication factor) ≈0.95. Spent fuel reprocessed by UREX+ method and then spiked with thorium and uranium composes the transmutation layer. The calculations were performed using MONTEBURNS code (MCNP5 and ORIGEN 2.1). The results indicate the best thickness and the volume ratio between the coolant and the fuel composition to induce transmutation.

  5. Historical perspective, economic analysis, and regulatory analysis of the impacts of waste partitioning-transmutation on the disposal of radioactive wastes

    Energy Technology Data Exchange (ETDEWEB)

    Forsberg, C.W.; Croff, A.G.; Kocher, D.C.

    1990-10-01

    Partitioning-transmutation, sometimes called actinide burning, is an alternative approach to high-level radioactive waste management. It consists of removing long-lived radionuclides from wastes and destroying those radionuclides, thus reducing the long-term hazards of radioactive waste. It was studied in detail in the 1970's. New developments in technology and other factors are resulting in a reexamination of this waste management option. This report consists of three papers which summarize the historical work, update the analysis of the costs of waste disposal, and describe current regulatory requirements which might be impacted by P-T. The papers provide a starting point for future research on P-T. 152 refs., 2 figs., 19 tabs.

  6. The Actinide Transition Revisited by Gutzwiller Approximation

    Science.gov (United States)

    Xu, Wenhu; Lanata, Nicola; Yao, Yongxin; Kotliar, Gabriel

    2015-03-01

    We revisit the problem of the actinide transition using the Gutzwiller approximation (GA) in combination with the local density approximation (LDA). In particular, we compute the equilibrium volumes of the actinide series and reproduce the abrupt change of density found experimentally near plutonium as a function of the atomic number. We discuss how this behavior relates with the electron correlations in the 5 f states, the lattice structure, and the spin-orbit interaction. Our results are in good agreement with the experiments.

  7. Predictive Modeling in Actinide Chemistry and Catalysis

    Energy Technology Data Exchange (ETDEWEB)

    Yang, Ping [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-05-16

    These are slides from a presentation on predictive modeling in actinide chemistry and catalysis. The following topics are covered in these slides: Structures, bonding, and reactivity (bonding can be quantified by optical probes and theory, and electronic structures and reaction mechanisms of actinide complexes); Magnetic resonance properties (transition metal catalysts with multi-nuclear centers, and NMR/EPR parameters); Moving to more complex systems (surface chemistry of nanomaterials, and interactions of ligands with nanoparticles); Path forward and conclusions.

  8. Lattice effects in the light actinides

    Energy Technology Data Exchange (ETDEWEB)

    Lawson, A.C.; Cort, B.; Roberts, J.A.; Bennett, B.I.; Brun, T.O.; Dreele, R.B. von [Los Alamos National Lab., NM (United States); Richardson, J.W. Jr. [Argonne National Lab., IL (United States)

    1998-12-31

    The light actinides show a variety of lattice effects that do not normally appear in other regions of the periodic table. The article will cover the crystal structures of the light actinides, their atomic volumes, their thermal expansion behavior, and their elastic behavior as reflected in recent thermal vibration measurements made by neutron diffraction. A discussion of the melting points will be given in terms of the thermal vibration measurements. Pressure effects will be only briefly indicated.

  9. Method and apparatus for transmutation of atomic nuclei

    Science.gov (United States)

    Maenchen, John Eric; Ruiz, Carlos Leon

    1998-01-01

    Insuring a constant supply of radioisotopes is of great importance to medicine and industry. This invention addresses this problem, and helps to solve it by introducing a new apparatus for transmutation of isotopes which enables swift and flexible production on demand.

  10. Advances in computational actinide chemistry in China

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Dongqi; Wu, Jingyi; Chai, Zhifang [Chinese Academy of Sciences, Beijing (China). Multidisciplinary Initiative Center; Su, Jing [Chinese Academy of Sciences, Shanghai (China). Div. of Nuclear Materials Science and Engineering; Li, Jun [Tsinghua Univ., Beijing (China). Dept. of Chemistry and Laboratory of Organic Optoelectronics and Molecular Engineering

    2014-04-01

    The advances in computational actinide chemistry made in China are reviewed. Several areas relevant to chemistry of actinides in gas, liquid, and solid phases have been explored. However, we limit the scope to selected contributions in the chemistry of molecular actinide systems in gas and liquid phases. These studies may be classified into two categories: treatment of relativistic effects, which cover the development of two- and four-component Hamiltonians and the optimization of relativistic pseudopotentials, and the applications of theoretical methods in actinide chemistry. The applications include (1) the electronic structures of actinocene, noble gas complexes, An-C multiple bonding compounds, uranyl and its isoelectronic species, fluorides and oxides, molecular systems with metal-metal bonding in their isolated forms (U{sub 2}, Pu{sub 2}) and in fullerene (U{sub 2} rate at C{sub 60}), and the excited states of actinide complexes; (2) chemical reactions, including oxidation, hydrolysis of UF{sub 6}, ligand exchange, reactivities of thorium oxo and sulfido metallocenes, CO{sub 2}/CS{sub 2} functionalization promoted by trivalent uranium complex; and (3) migration of actinides in the environment. A future outlook is discussed. (orig.)

  11. A comparison of radioactive waste from first generation fusion reactors and fast fission reactors with actinide recycling

    Energy Technology Data Exchange (ETDEWEB)

    Koch, M.; Kazimi, M.S.

    1991-04-01

    Limitations of the fission fuel resources will presumably mandate the replacement of thermal fission reactors by fast fission reactors that operate on a self-sufficient closed fuel cycle. This replacement might take place within the next one hundred years, so the direct competitors of fusion reactors will be fission reactors of the latter rather than the former type. Also, fast fission reactors, in contrast to thermal fission reactors, have the potential for transmuting long-lived actinides into short-lived fission products. The associated reduction of the long-term activation of radioactive waste due to actinides makes the comparison of radioactive waste from fast fission reactors to that from fusion reactors more rewarding than the comparison of radioactive waste from thermal fission reactors to that from fusion reactors. Radioactive waste from an experimental and a commercial fast fission reactor and an experimental and a commercial fusion reactor has been characterized. The fast fission reactors chosen for this study were the Experimental Breeder Reactor 2 and the Integral Fast Reactor. The fusion reactors chosen for this study were the International Thermonuclear Experimental Reactor and a Reduced Activation Ferrite Helium Tokamak. The comparison of radioactive waste parameters shows that radioactive waste from the experimental fast fission reactor may be less hazardous than that from the experimental fusion reactor. Inclusion of the actinides would reverse this conclusion only in the long-term. Radioactive waste from the commercial fusion reactor may always be less hazardous than that from the commercial fast fission reactor, irrespective of the inclusion or exclusion of the actinides. The fusion waste would even be far less hazardous, if advanced structural materials, like silicon carbide or vanadium alloy, were employed.

  12. Preparation of a technology development roadmap for the Accelerator Transmutation of Waste (ATW) System : report of the ATW separations technologies and waste forms technical working group.

    Energy Technology Data Exchange (ETDEWEB)

    Collins, E.; Duguid, J.; Henry, R.; Karell, E.; Laidler, J.; McDeavitt, S.; Thompson, M.; Toth, M.; Williamson, M.; Willit, J.

    1999-08-12

    In response to a Congressional mandate to prepare a roadmap for the development of Accelerator Transmutation of Waste (ATW) technology, a Technical Working Group comprised of members from various DOE laboratories was convened in March 1999 for the purpose of preparing that part of the technology development roadmap dealing with the separation of certain radionuclides for transmutation and the disposal of residual radioactive wastes from these partitioning operations. The Technical Working Group for ATW Separations Technologies and Waste Forms completed its work in June 1999, having carefully considered the technology options available. A baseline process flowsheet and backup process were identified for initial emphasis in a future research, development and demonstration program. The baseline process combines aqueous and pyrochemical processes to permit the efficient separation of the uranium, technetium, iodine and transuranic elements from the light water reactor (LWR) fuel in the head-end step. The backup process is an all- pyrochemical system. In conjunction with the aqueous process, the baseline flowsheet includes a pyrochemical process to prepare the transuranic material for fabrication of the ATW fuel assemblies. For the internal ATW fuel cycle the baseline process specifies another pyrochemical process to extract the transuranic elements, Tc and 1 from the ATW fuel. Fission products not separated for transmutation and trace amounts of actinide elements would be directed to two high-level waste forms, one a zirconium-based alloy and the other a glass/sodalite composite. Baseline cost and schedule estimates are provided for a RD&D program that would provide a full-scale demonstration of the complete separations and waste production flowsheet within 20 years.

  13. Damages in ceramics for nuclear waste transmutation by irradiation with swift heavy ions

    Science.gov (United States)

    Beauvy, Michel; Dalmasso, Chrystelle; Thiriet-Dodane, Catherine; Simeone, David; Gosset, Dominique

    2006-01-01

    Inert matrices are proposed for advanced nuclear fuels or for the transmutation of the actinides that is an effective solution for the nuclear waste management. The behaviour of inert matrix ceramics like MgO, MgAl2O4 and cubic ZrO2 oxides under irradiation is presented in this study. The alumina Al2O3 has been also studied as a reference for the ceramic materials. These oxides have been irradiated with swift heavy ions at CIRIL/GANIL to simulate the fragment fission effects. The irradiations with the different heavy ions (from S to Pb) with energy between 91 and 820 MeV, have been realised at room temperature or 500 °C. The fluencies were between 5 × 1010 and 5 × 1015 ions/cm2. The polished faces of sintered polycrystalline disks or single crystal slices have been characterized before and after irradiation by X-ray diffraction and optical spectroscopy. The apparent swelling evaluated from surface profile measurements after irradiation is very important for spinel and zirconia, comparatively with those of magnesia or alumina. The amorphisation seems to be at the origin of this swelling, and the electronic stopping power of the ions is the most influent parameter for the irradiation damages. The point defects characterized by optical spectroscopy show a significant amount of damage on the oxygen sub-lattice in the irradiated oxides. F+ centres are present in all irradiated oxides. However, new absorption bands are observed and cation clusters cannot be excluded in magnesia and spinel after irradiation.

  14. PF-4 actinide disposition strategy

    Energy Technology Data Exchange (ETDEWEB)

    Margevicius, Robert W [Los Alamos National Laboratory

    2010-05-28

    The dwindling amount of Security Category I processing and storage space across the DOE Complex has driven the need for more effective storage of nuclear materials at LANL's Plutonium Facility's (PF-4's) vault. An effort was begun in 2009 to create a strategy, a roadmap, to identify all accountable nuclear material and determine their disposition paths, the PF-4 Actinide Disposition Strategy (PADS). Approximately seventy bins of nuclear materials with similar characteristics - in terms of isotope, chemical form, impurities, disposition location, etc. - were established in a database. The ultimate disposition paths include the material to remain at LANL, disposition to other DOE sites, and disposition to waste. If all the actions described in the document were taken, over half of the containers currently in the PF-4 vault would been eliminated. The actual amount of projected vault space will depend on budget and competing mission requirements, however, clearly a significant portion of the current LANL inventory can be either dispositioned or consolidated.

  15. Managing Zirconium Chemistry and Phase Compatibility in Combined Process Separations for Minor Actinide Partitioning

    Energy Technology Data Exchange (ETDEWEB)

    Wall, Nathalie [Washington State Univ., Pullman, WA (United States); Nash, Ken [Washington State Univ., Pullman, WA (United States); Martin, Leigh [Washington State Univ., Pullman, WA (United States)

    2017-03-17

    In response to the NEUP Program Supporting Fuel Cycle R&D Separations and Waste Forms call DEFOA- 0000799, this report describes the results of an R&D project focusing on streamlining separation processes for advanced fuel cycles. An example of such a process relevant to the U.S. DOE FCR&D program would be one combining the functions of the TRUEX process for partitioning of lanthanides and minor actinides from PUREX(UREX) raffinates with that of the TALSPEAK process for separating transplutonium actinides from fission product lanthanides. A fully-developed PUREX(UREX)/TRUEX/TALSPEAK suite would generate actinides as product(s) for reuse (or transmutation) and fission products as waste. As standalone, consecutive unit-operations, TRUEX and TALSPEAK employ different extractant solutions (solvating (CMPO, octyl(phenyl)-N,Ndiisobutylcarbamoylmethylphosphine oxide) vs. cation exchanging (HDEHP, di-2(ethyl)hexylphosphoric acid) extractants), and distinct aqueous phases (2-4 M HNO3 vs. concentrated pH 3.5 carboxylic acid buffers containing actinide selective chelating agents). The separate processes may also operate with different phase transfer kinetic constraints. Experience teaches (and it has been demonstrated at the lab scale) that, with proper control, multiple process separation systems can operate successfully. However, it is also recognized that considerable economies of scale could be achieved if multiple operations could be merged into a single process based on a combined extractant solvent. The task of accountability of nuclear materials through the process(es) also becomes more robust with fewer steps, providing that the processes can be accurately modeled. Work is underway in the U.S. and Europe on developing several new options for combined processes (TRUSPEAK, ALSEP, SANEX, GANEX, ExAm are examples). There are unique challenges associated with the operation of such processes, some relating to organic phase chemistry, others arising from the

  16. TUCS/phosphate mineralization of actinides

    Energy Technology Data Exchange (ETDEWEB)

    Nash, K.L. [Argonne National Lab., IL (United States)

    1997-10-01

    This program has as its objective the development of a new technology that combines cation exchange and mineralization to reduce the concentration of heavy metals (in particular actinides) in groundwaters. The treatment regimen must be compatible with the groundwater and soil, potentially using groundwater/soil components to aid in the immobilization process. The delivery system (probably a water-soluble chelating agent) should first concentrate the radionuclides then release the precipitating anion, which forms thermodynamically stable mineral phases, either with the target metal ions alone or in combination with matrix cations. This approach should generate thermodynamically stable mineral phases resistant to weathering. The chelating agent should decompose spontaneously with time, release the mineralizing agent, and leave a residue that does not interfere with mineral formation. For the actinides, the ideal compound probably will release phosphate, as actinide phosphate mineral phases are among the least soluble species for these metals. The most promising means of delivering the precipitant would be to use a water-soluble, hydrolytically unstable complexant that functions in the initial stages as a cation exchanger to concentrate the metal ions. As it decomposes, the chelating agent releases phosphate to foster formation of crystalline mineral phases. Because it involves only the application of inexpensive reagents, the method of phosphate mineralization promises to be an economical alternative for in situ immobilization of radionuclides (actinides in particular). The method relies on the inherent (thermodynamic) stability of actinide mineral phases.

  17. Numerical analysis on reduction of radioactive actinides by recycling of nuclear fuel; Analisis numerico sobre reduccion de actinidos radiactivos por reciclado de combustible nuclear

    Energy Technology Data Exchange (ETDEWEB)

    Balboa L, H. E.

    2014-07-01

    Worldwide, human growth has reached unparalleled levels historically, this implies a need for more energy, and just in 2007 was consumed in the USA 4157 x 10{sup 9} kWh of electricity and there were 6 x 10{sup 9} metric tons of carbon dioxide, which causes a devastating effect on our environment. To this problem, a solution to the demand for non-fossil energy is nuclear energy, which is one of the least polluting and the cheapest among non-fossil energy; however, a problem remains unresolved the waste generation of nuclear fuels. In this work the option of a possible transmutation of actinides in a nuclear reactor of BWR was analyzed, an example of this are the nuclear reactors at the Laguna Verde nuclear power plant, which have generated spent fuel stored in pools awaiting a decision for final disposal or any other existing alternative. Assuming that the spent fuel was reprocessed to separate useful materials and actinides such as plutonium and uranium remaining, could take these actinides and to recycle them inside the same reactor that produced them, so il will be reduced the radiotoxicity of spent fuel. The main idea of this paper is to evaluate by means of numeric simulation (using the Core Management System (CMS)) the reduction of minor actinides in the case of being recycled in fresh fuel of the type BWR. The actinides were introduced hypothetically in the fuel pellets to 6% by weight, and then use a burned in the range of 0-65 G Wd/Tm, in order to have a better panorama of their behavior and thus know which it is the best choice for maximum reduction of actinides. Several cases were studied, that is to say were used as fuels; the UO{sub 2} and MOX. Six different cases were also studied to see the behavior of actinides in different situations. The CMS platform calculation was used for the analysis of the cases presented. Favorable results were obtained, having decreased from a range of 35% to 65% of minor actinides initially introduced in the fuel rods

  18. Actinide Partitioning-Transmutation Program Final Report. V. Preconceptual designs and costs of partitioning facilities and shipping casks (appendix 3)

    Energy Technology Data Exchange (ETDEWEB)

    1980-06-01

    This Appendix contains cost estimate documents for the Fuels Reprocessing Plant Waste Treatment Facility. Plant costs are summarized by Code of Accounts and by Process Function. Costs contribution to each account are detailed. Process equipment costs are detailed for each Waste Treatment Process. Service utility costs are also summarized and detailed.

  19. System and safety studies of accelerator driven systems and generation IV reactors for transmutation of minor actinides. Annual report 2009

    Energy Technology Data Exchange (ETDEWEB)

    Bergloef, Calle; Fokau, Andrei; Jolkkonen, Mikael; Tesinsky, Milan; Wallenius, Janne; Youpeng Zhang (Div. of Reactor Physics, Royal Institute of Technology, Stockholm (Sweden))

    2010-03-15

    During 2009, the reactor physics division has made a design study of a source efficient ADS with nitride fuel and 15/15Ti cladding, based on the EFIT design made within the EUROTRANS project. It was shown that the source efficiency may be doubled as compared to the reference design with oxide fuel and T91 cladding. Transient analysis of a medium sized sodium cooled reactor with MOX fuel allowed to define criteria in terms of power penalty for americium introduction. It was shown that for each percent of americium added to the fuel, the linear rating must be reduced by 6% in order for the fuel to survive postulated unprotected transients. The Sjoestrand area ratio method for reactivity determination has been evaluated experimentally in the strongly heterogeneous subcritical facility YALINA-Booster. Surprisingly, it has been found that the area ratio reactivity estimates may differ by a factor of two depending on detector position. It is shown that this strong spatial dependence can be explained based on a two-region point kinetics model and rectified by means of correction factors obtained through Monte Carlo simulations. For the purpose of measuring high energy neutron cross sections at the SCANDAL facility in Uppsala, Monte Carlo simulations of neutron to proton conversion efficiencies in CsI detectors have been performed. A uranium fuel fabrication laboratory has been taken into operation at KTH in 2009. Uranium and zirconium nitride powders have been fabricated by hydridation/nitridation of metallic source materials. Sample pellets have been pressed and ZrN discs have been sintered to 93% density by means of spark plasma sintering methods

  20. Transmutation of nuclear waste with a low-aspect-ratio Tokamak neutron source

    Energy Technology Data Exchange (ETDEWEB)

    Hong, Bong Guen; Moon, Se Youn [Chonbuk National University, Jeonju (Korea, Republic of)

    2014-10-15

    The transmutation characteristics of transuranics (TRUs) in a transmutation reactor based on a LAR (Low-aspect-ratio) tokamak as a neutron source are investigated. The optimum radial build of a transmutation reactor is found by using a coupled analysis of the tokamak systems and the neutron transport. The dependences of the transmutation characteristics on the aspect ratio A in the range of 1.5 to 2.5 and on the fusion power in the range of 150 to 500 MW are investigated. An equilibrium fuel cycle is developed for effective transmutation, and show that with one unit of the transmutation reactor based on the LAR tokamak producing fusion power in the range of a few hundred MWs, up to 3 PWRs (1.0 GWe capacity) can be supported with a burn-up fraction larger than 50%.

  1. Transmutation of nuclear waste with a low-aspect-ratio tokamak neutron source

    Science.gov (United States)

    Hong, Bong Guen; Moon, Se Youn

    2014-10-01

    The transmutation characteristics of transuranics (TRUs) in a transmutation reactor based on a LAR (Low-aspect-ratio) tokamak as a neutron source are investigated. The optimum radial build of a transmutation reactor is found by using a coupled analysis of the tokamak systems and the neutron transport. The dependences of the transmutation characteristics on the aspect ratio A in the range of 1.5 to 2.5 and on the fusion power in the range of 150 to 500 MW are investigated. An equilibrium fuel cycle is developed for effective transmutation, and show that with one unit of the transmutation reactor based on the LAR tokamak producing fusion power in the range of a few hundred MWs, up to 3 PWRs (1.0 GWe capacity) can be supported with a burn-up fraction larger than 50%.

  2. System and safety studies of accelerator driven transmutation systems

    Energy Technology Data Exchange (ETDEWEB)

    Gudowski, W.; Wallenius, J.; Tucek, K.; Eriksson, Marcus; Carlsson, Johan; Seltborg, P.; Cetnar, J. [Royal Inst. of Technology, Stockholm (Sweden). Dept. of Nuclear and Reactor Physics

    2001-05-01

    The research on safety of Accelerator-Driven Transmutation Systems (ADS) at the department has been focused on: a) ADS core design and development of advanced nuclear fuel optimised for high transmutation rates and good safety features; b) analysis of ADS-dynamics c) computer code and nuclear data development relevant for simulation and optimization of ADS; d) participation in ADS experiments including 1 MW spallation target manufacturing, subcritical experiments MUSE (CEA-Cadarache). Moreover, during the reporting period the EU-project 'IABAT', co-ordinated by the department has been finished and 4 other projects have been initiated in the frame of the 5th European Framework Programme. Most of the research topics reported in this paper are referred to appendices, which have been published in the open literature. The topics, which are not yet published, are described here in more details.

  3. Electronic Structure of the Actinide Metals

    DEFF Research Database (Denmark)

    Johansson, B.; Skriver, Hans Lomholt

    1982-01-01

    Some recent experimental photoelectron spectroscopic results for the actinide metals are reviewed and compared with the theoretical picture of the basic electronic structure that has been developed for the actinides during the last decade. In particular the experimental data confirm the change from...... itinerant to localized 5f electron behaviour calculated to take place between plutonium and americium. From experimental data it is shown that the screening of deep core-holes is due to 5f electrons for the lighter actinide elements and 6d electrons for the heavier elements. A simplified model for the full...... LMTO electronic structure calculations is introduced. In this model the spd and 5f electronic contributions are treated as separable entities. It is shown that the model reproduces quite well the results from the full treatment. The equilibrium volume, cohesive energy and bulk modulus are calculated...

  4. Monazite as a suitable actinide waste form

    Energy Technology Data Exchange (ETDEWEB)

    Schlenz, Hartmut; Heuser, Julia; Schmitz, Stephan; Bosbach, Dirk [Forschungszentrum Juelich GmbH (Germany). Inst. fuer Energie und Klimaforschung (IEK), Nukleare Entsorgung und Reaktorsicherheit (IEK-6); Neumann, Andreas [Forschungszentrum Juelich GmbH (Germany). Inst. fuer Energie und Klimaforschung (IEK), Nukleare Entsorgung und Reaktorsicherheit (IEK-6); RWTH Aachen Univ. (Germany). Inst. for Crystallography

    2013-03-01

    The conditioning of radioactive waste from nuclear power plants and in some countries even of weapons plutonium is an important issue for science and society. Therefore the research on appropriate matrices for the immobilization of fission products and actinides is of great interest. Beyond the widely used borosilicate glasses, ceramics are promising materials for the conditioning of actinides like U, Np, Pu, Am, and Cm. Monazite-type ceramics with general composition LnPO{sub 4} (Ln = La to Gd) and solid solutions of monazite with cheralite or huttonite represent important materials in this field. Monazite appears to be a promising candidate material, especially because of its outstanding properties regarding radiation resistance and chemical durability. This article summarizes the most recent results concerning the characterization of monazite and respective solid solutions and the study of their chemical, thermal, physical and structural properties. The aim is to demonstrate the suitability of monazite as a secure and reliable waste form for actinides. (orig.)

  5. Spatial heterogeneity of tungsten transmutation in a fusion device

    Science.gov (United States)

    Gilbert, M. R.; Sublet, J.-Ch.; Dudarev, S. L.

    2017-04-01

    Accurately quantifying the transmutation rate of tungsten (W) under neutron irradiation is a necessary requirement in the assessment of its performance as an armour material in a fusion power plant. The usual approach of calculating average responses, assuming large, homogenised material volumes, is insufficient to capture the full complexity of the transmutation picture in the context of a realistic fusion power plant design, particularly for rhenium (Re) production from W. Combined neutron transport and inventory simulations for representative spatially heterogeneous high-resolution models of a fusion power plant show that the production rate of Re is strongly influenced by the surrounding local spatial environment. Localised variation in neutron moderation (slowing down) due to structural steel and coolant, particularly water, can dramatically increase Re production because of the huge cross sections of giant resolved resonances in the neutron-capture reaction of 186W at low neutron energies. Calculations using cross section data corrected for temperature (Doppler) effects suggest that temperature may have a relatively lesser influence on transmutation rates.

  6. Spin–orbit coupling in actinide cations

    DEFF Research Database (Denmark)

    Bagus, Paul S.; Ilton, Eugene S.; Martin, Richard L.

    2012-01-01

    The limiting case of Russell–Saunders coupling, which leads to a maximum spin alignment for the open shell electrons, usually explains the properties of high spin ionic crystals with transition metals. For actinide compounds, the spin–orbit splitting is large enough to cause a significantly reduced...... spin alignment. Novel concepts are used to explain the dependence of the spin alignment on the 5f shell occupation. We present evidence that the XPS of ionic actinide materials may provide direct information about the angular momentum coupling within the 5f shell....

  7. Utilization of Minor Actinides as a Fuel Component for Ultra-Long Life Bhr Configurations: Designs, Advantages and Limitations

    Energy Technology Data Exchange (ETDEWEB)

    Dr. Pavel V. Tsvetkov

    2009-05-20

    This project assessed the advantages and limitations of using minor actinides as a fuel component to achieve ultra-long life Very High Temperature Reactor (VHTR) configurations. Researchers considered and compared the capabilities of pebble-bed and prismatic core designs with advanced actinide fuels to achieve ultra-long operation without refueling. Since both core designs permit flexibility in component configuration, fuel utilization, and fuel management, it is possible to improve fissile properties of minor actinides by neutron spectrum shifting through configuration adjustments. The project studied advanced actinide fuels, which could reduce the long-term radio-toxicity and heat load of high-level waste sent to a geologic repository and enable recovery of the energy contained in spent fuel. The ultra-long core life autonomous approach may reduce the technical need for additional repositories and is capable to improve marketability of the Generation IV VHTR by allowing worldwide deployment, including remote regions and regions with limited industrial resources. Utilization of minor actinides in nuclear reactors facilitates developments of new fuel cycles towards sustainable nuclear energy scenarios.

  8. EASY-II: a system for modelling of n, d, p, {\\gamma} and {\\alpha} activation and transmutation processes

    CERN Document Server

    Sublet, Jean-Christophe; Morgan, Guy; Koning, Arjan; Rochman, Dimitri

    2013-01-01

    EASY-II is designed as a functional replacement for the previous European Activation System, EASY-2010. It has extended nuclear data and new software, FISPACT-II, written in object-style Fortran to provide new capabilities for predictions of activation, transmutation, depletion and burnup. The new FISPACT-II code has allowed us to implement many more features in terms of energy range, up to GeV; incident particles: alpha, gamma, proton, deuteron and neutron; and neutron physics: self-shielding effects, temperature dependence, pathways analysis, sensitivity and error estimation using covariance data. These capabilities cover most application needs: nuclear fission and fusion, accelerator physics, isotope production, waste management and many more. In parallel, the maturity of modern general-purpose libraries such as TENDL-2012 encompassing thousands of target nuclides, the evolution of the ENDF format and the capabilities of the latest generation of processing codes PREPRO-2012, NJOY2012 and CALENDF-2010 have ...

  9. Neutron-induced capture cross sections of short-lived actinides with the surrogate reaction method

    Directory of Open Access Journals (Sweden)

    Gunsing F.

    2010-03-01

    Full Text Available Determination of neutron-capture cross sections of short-lived nuclei is opening the way to understand and clarify the properties of many nuclei of interest for nuclear structure physics, nuclear astrophysics and particularly for transmutation of nuclear wastes. The surrogate approach is well-recognized as a potentially very useful method to extract neutron cross sections for low-energy compound-nuclear reactions and to overcome the difficulties related to the target radioactivity. In this work we will assess where we stand on these neutron-capture cross section measurements and how we can achieve the short-lived Minor Actinides nuclei involved in the nuclear fuel cycle. The CENBG collaboration applied the surrogate method to determine the neutron-capture cross section of 233Pa (T1/2 = 27 d. The 233Pa (n,γ cross section is then deduced from the measured gamma decay probability of 234Pa compound nucleus formed via the surrogate 232Th(3He,p reaction channel. The obtained cross section data, covering the neutron energy range 0.1 to 1 MeV, have been compared with the predictions of the Hauser-Feshbach statistical model. The importance of establishing benchmarks is stressed for the minor actinides region. However, the lack of desired targets led us to propose recently the 174Yb (3He,pγ reaction as a surrogate reaction for the (n,γ predetermined benchmark cross section of 175Lu. An overview of the experimental setup combining gamma ray detectors such as Ge and C6D6 in coincidence with light charged particles ΔE-E Telescopes will be presented and preliminary results will be discussed.

  10. Researches on the management of high activity and long-lived radioactive wastes. Axis 1 - separation-transmutation; Recherches sur la gestion des dechets radioactifs a haute activite et a vie longue. Axe 1 - separation-transmutation

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2005-11-15

    This document gathers the transparencies of seven presentations given at a technical workshop of the French nuclear energy society (SFEN) about the researches on separation-transmutation of high activity and long-lived radioactive wastes. The presentations deal with: inventory and radiotoxicity of the rad-wastes in concern; industrial experience; experience on chemical separation: molecules and processes; reactors physics and transmutation - reactors for transmutation; fuels and targets; scenarios that include transmutation; environmental impacts of these different scenarios. (J.S.)

  11. Actinide valences in xenotime and monazite

    Energy Technology Data Exchange (ETDEWEB)

    Vance, E.R. [Institute of Materials Engineering, Australian Nuclear Science and Technology Organisation, Locked Bag 2001 Kirrawee DC, NSW 2232 (Australia); Zhang, Y., E-mail: yzx@ansto.gov.au [Institute of Materials Engineering, Australian Nuclear Science and Technology Organisation, Locked Bag 2001 Kirrawee DC, NSW 2232 (Australia); McLeod, T.; Davis, J. [Institute of Materials Engineering, Australian Nuclear Science and Technology Organisation, Locked Bag 2001 Kirrawee DC, NSW 2232 (Australia)

    2011-02-28

    Tetravalent U, Np and Pu can be substituted by ceramic methods into the rare earth site of xenotime and monazite in air atmospheres using Ca ions as charge compensators, while no evidence of penta- or hexavalent actinide ions was found. Some Pu{sup 3+} and Np{sup 3+} can be incorporated in xenotime samples fired in a reducing atmosphere.

  12. Scalar Static Polarizabilities of Lanthanides and Actinides

    CERN Document Server

    Dzuba, V A; Flambaum, V V

    2014-01-01

    We calculate scalar static polarizabilities for lanthanides and actinides, the atoms with open $4f$ or $5f$ subshell. We show that polarizabilities of the low states are approximately the same for all states of given configuration and present a way of calculating them reducing valence space to just two or three valence electrons occupying $6s$ and $5d$ states for lanthanides or $7s$ and $6d$ states for actinides while $4f$ and $5f$ states are considered to be in the core. Configuration interaction technique is used to calculate polarizabilities of lanthanides and actinides for all states of the $4f^n6s^2$ and $4f^{n-1}6s^25d$ configurations of lanthanides and all states of the $5f^{n}7s^2$ and $5f^{n-1}7s^26d$ configurations of actinides. Polarizability of the electron core (including f-orbitals) has been calculated in the RPA approximation.

  13. Actinide measurements by AMS using fluoride matrices

    Energy Technology Data Exchange (ETDEWEB)

    Cornett, R.J., E-mail: Jack.Cornett@uottawa.ca [André E. Lalonde AMS Laboratory, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Department of Earth Sciences, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Kazi, Z.H. [André E. Lalonde AMS Laboratory, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Department of Earth Sciences, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Zhao, X.-L. [André E. Lalonde AMS Laboratory, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Department of Physics, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Chartrand, M.G. [André E. Lalonde AMS Laboratory, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Department of Earth Sciences, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Charles, R.J.; Kieser, W.E. [André E. Lalonde AMS Laboratory, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada); Department of Physics, University of Ottawa, 150 Louis Pasteur, Ottawa, ON K1N 6N5 (Canada)

    2015-10-15

    Actinides can be measured by alpha spectroscopy (AS), mass spectroscopy or accelerator mass spectrometry (AMS). We tested a simple method to separate Pu and Am isotopes from the sample matrix using a single extraction chromatography column. The actinides in the column eluent were then measured by AS or AMS using a fluoride target matrix. Pu and Am were coprecipitated with NdF{sub 3}. The strongest AMS beams of Pu and Am were produced when there was a large excess of fluoride donor atoms in the target and the NdF{sub 3} precipitates were diluted about 6–8 fold with PbF{sub 2}. The measured concentrations of {sup 239,240}Pu and {sup 241}Am agreed with the concentrations in standards of known activity and with two IAEA certified reference materials. Measurements of {sup 239,240}Pu and {sup 241}Am made at A.E. Lalonde AMS Laboratory agree, within their statistical uncertainty, with independent measurements made using the IsoTrace AMS system. This work demonstrated that fluoride targets can produce reliable beams of actinide anions and that the measurement of actinides using fluorides agree with published values in certified reference materials.

  14. Nuclear transmutation strategies for management of long-lived fission products

    Indian Academy of Sciences (India)

    S Kailas; M Hemalatha; A Saxena

    2015-09-01

    Management of long-lived nuclear waste produced in a reactor is essential for long-term sustenance of nuclear energy programme. A number of strategies are being explored for the effective transmutation of long-lived nuclear waste in general, and long-lived fission products (LLFP), in particular. Some of the options available for the transmutation of LLFP are discussed.

  15. System and safety studies of accelerator driven transmutation. Annual Report 2002

    Energy Technology Data Exchange (ETDEWEB)

    Gudowski, W.; Wallenius, J.; Tucek, K.; Eriksson, Marcus; Carlsson, Johan; Seltborg, P.; Cetnar, J.; Chakarova, R.; Jollkonen, Mikael; Westlen, D. [Royal Inst. of Technology, Stockholm (Sweden). Dept. of Nuclear and Reactor Physics

    2003-06-01

    possibly drive the system prompt critical. This is an improbable event due to the high boiling temperature of Pb/Bi but requires attention. Minor actinide transmutation in ADS: Presence of 30-40% plutonium, in order to achieve a minimum reactivity swing, combined with an average inert matrix volume fraction larger than 50%, in order to ensure fabricability and obtain a suitable sub-criticality level. A Tungsten matrix does not seem to fulfill this condition; A high thermal conductivity combined with a high melting temperature, in order to provide a high power to melt. Sodium bonded nitride has an outstanding performance in this context; A small cross section for in-elastic scattering combined with a high thermal conductivity minimizes void worth. Inert matrix of Cr or YN yields close to zero void worth for the configurations investigated; A high probability for fission of Am minimizes buildup of curium. Hafnium nitride gives the highest fission probability compared to ZrN and YN; Some reduction of 210 Po concentration can be easily obtained by introduction of reflectors and absorbers in the core periphery. Some improvement can be also obtained by moderation of the flux by beryllium. However, other means will be necessary to achieve significant {sup 210}Po activity reduction satisfying radiation protection requirements. The highest irradiation of the internals located above and below the core with the damage peaking close to the reactor axis due to the closest distance to the core centre is observed; radiation damage on the core diagrid over 20 years of operations is lower than 0.4 DPA for a local peaking point; radiation damage on regions of restraint plate (not replaceable) stays also well below the limit and can reach 0.4 DPA for a local peaking point. The reduction of it if Be-SS-B4C periphery arrangement is introduced can be by factor of 10 to 0.04 DPA; other solutions of core periphery (without neutron moderation) have no potential for lowering the DPA at central

  16. System and safety studies of accelerator driven transmutation. Annual Report 2002

    Energy Technology Data Exchange (ETDEWEB)

    Gudowski, W.; Wallenius, J.; Tucek, K.; Eriksson, Marcus; Carlsson, Johan; Seltborg, P.; Cetnar, J.; Chakarova, R.; Jollkonen, Mikael; Westlen, D. [Royal Inst. of Technology, Stockholm (Sweden). Dept. of Nuclear and Reactor Physics

    2003-06-01

    possibly drive the system prompt critical. This is an improbable event due to the high boiling temperature of Pb/Bi but requires attention. Minor actinide transmutation in ADS: Presence of 30-40% plutonium, in order to achieve a minimum reactivity swing, combined with an average inert matrix volume fraction larger than 50%, in order to ensure fabricability and obtain a suitable sub-criticality level. A Tungsten matrix does not seem to fulfill this condition; A high thermal conductivity combined with a high melting temperature, in order to provide a high power to melt. Sodium bonded nitride has an outstanding performance in this context; A small cross section for in-elastic scattering combined with a high thermal conductivity minimizes void worth. Inert matrix of Cr or YN yields close to zero void worth for the configurations investigated; A high probability for fission of Am minimizes buildup of curium. Hafnium nitride gives the highest fission probability compared to ZrN and YN; Some reduction of 210 Po concentration can be easily obtained by introduction of reflectors and absorbers in the core periphery. Some improvement can be also obtained by moderation of the flux by beryllium. However, other means will be necessary to achieve significant {sup 210}Po activity reduction satisfying radiation protection requirements. The highest irradiation of the internals located above and below the core with the damage peaking close to the reactor axis due to the closest distance to the core centre is observed; radiation damage on the core diagrid over 20 years of operations is lower than 0.4 DPA for a local peaking point; radiation damage on regions of restraint plate (not replaceable) stays also well below the limit and can reach 0.4 DPA for a local peaking point. The reduction of it if Be-SS-B4C periphery arrangement is introduced can be by factor of 10 to 0.04 DPA; other solutions of core periphery (without neutron moderation) have no potential for lowering the DPA at central

  17. Adventures in Actinide Chemistry: A Year of Exploring Uranium and Thorium in Los Alamos

    Energy Technology Data Exchange (ETDEWEB)

    Pagano, Justin [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2016-01-08

    The first part of this collection of slides is concerned with considerations when working with actinides. The topics discussed in the document as a whole are the following: Actinide chemistry vs. transition metal chemistry--tools we can use; New synthetic methods to obtain actinide hydrides; Actinide metallacycles: synthesis, structure, and properties; and Reactivity of actinide metallacycles.

  18. Photo-transmutation of {sup 100}Mo to {sup 99}Mo with Laser-Compton Scattering Gamma-ray

    Energy Technology Data Exchange (ETDEWEB)

    Lee, Jiyoung; Rehman, Haseeb ur; Kim, Yonghee [KAIST, Daejeon (Korea, Republic of)

    2016-10-15

    This paper presents a photonuclear transmutation method using laser Compton scattering (LCS) gamma-ray beam. Potential production rate (reaction rate) of 99Mo using the photonuclear (γ,n) reaction is evaluated. Rigorous optimization of the LCS spectrum has also been performed to maximize production of the 99Mo. Cyclotron proton accelerators are used worldwide to produce many short-living medical isotopes. However, few are capable of producing Mo-99 and none are suitable for producing more than a small fraction of the required amounts. More than 90% of the world's demand of 99Mo is sourced from five nuclear reactors. Two of these reactors have already been decommissioned and the rest are more than 45 years old. Relatively short half-life of the parent 99Mo requires continuous re-supply to meet the requirements of medical industry. Therefore, there is an urgent need to produce the 99Mo and 99mTc isotopes by alternative ways. One such alternative is giant dipole resonance (GDR) based photonuclear transmutation of 100Mo to 99Mo. For 99Mo production with the LCS photons using GDR-based (γ,n) reaction, the gamma-ray energy should be around 15 MeV. This study indicates that optimization of LCS spectrum by varying the electron and laser energies within practical limits can enhance the transmutation of Mo-100 to M-99 quite significantly. It has been found that irradiation time should be rather short, e.g., less than 6 hours, to maximize the weekly production of Mo-99 in the GDR-based Mo-99 production facility using the LCS photons. The analysis shows that production of 99Mo using a high-performance LCS facility offers a potentially-promising alternative for the production of 99mTc.

  19. Synthesis of actinide nitrides, phosphides, sulfides and oxides

    Science.gov (United States)

    Van Der Sluys, William G.; Burns, Carol J.; Smith, David C.

    1992-01-01

    A process of preparing an actinide compound of the formula An.sub.x Z.sub.y wherein An is an actinide metal atom selected from the group consisting of thorium, uranium, plutonium, neptunium, and americium, x is selected from the group consisting of one, two or three, Z is a main group element atom selected from the group consisting of nitrogen, phosphorus, oxygen and sulfur and y is selected from the group consisting of one, two, three or four, by admixing an actinide organometallic precursor wherein said actinide is selected from the group consisting of thorium, uranium, plutonium, neptunium, and americium, a suitable solvent and a protic Lewis base selected from the group consisting of ammonia, phosphine, hydrogen sulfide and water, at temperatures and for time sufficient to form an intermediate actinide complex, heating said intermediate actinide complex at temperatures and for time sufficient to form the actinide compound, and a process of depositing a thin film of such an actinide compound, e.g., uranium mononitride, by subliming an actinide organometallic precursor, e.g., a uranium amide precursor, in the presence of an effectgive amount of a protic Lewis base, e.g., ammonia, within a reactor at temperatures and for time sufficient to form a thin film of the actinide compound, are disclosed.

  20. System and safety studies of accelerator driven transmutation systems. Annual report 1999

    Energy Technology Data Exchange (ETDEWEB)

    Gudowski, Waclaw; Wallenius, Jan; Eriksson, Marcus; Carlsson, Johan; Seltborg, Per; Tucek, Kamil [Royal Inst. of Tech., Stockholm (Sweden). Dept. of Nuclear and Reactor Physics

    2000-05-01

    In 1996, SKB commenced funding of the project 'System and safety studies of accelerator driven transmutation systems and development of a spallation target'. The aim of the project was stated as: Development of a complete code for simulation of transmutation processes in an accelerator driven system. Application of the code for analysis of neutron flux, transmutation rates, reactivity changes, toxicity and radiation damages in the transmutation core. Build up of competence regarding issues related to spallation targets, development of research activities regarding relevant material issues. Performing of basic experiments in order to investigate the adequacy of using the spallation. target as a neutron source for a transmutation system, and participation in the planning and implementation of an international demonstration experiment. In the present report, activities within and related to the framework of the project, performed at the department of Nuclear and Reactor Physics at the Royal Institute of Technology during 1999, are accounted for.

  1. Feasibility study of nuclear transmutation by negative muon capture reaction using the PHITS code

    Science.gov (United States)

    Abe, Shin-ichiro; Sato, Tatsuhiko

    2016-06-01

    Feasibility of nuclear transmutation of fission products in high-level radioactive waste by negative muon capture reaction is investigated using the Particle and Heave Ion Transport code System (PHITS). It is found that about 80 % of stopped negative muons contribute to transmute target nuclide into stable or short-lived nuclide in the case of 135Cs, which is one of the most important nuclide in the transmutation. The simulation result also indicates that the position of transmutation is controllable by changing the energy of incident negative muon. Based on our simulation, it takes approximately 8.5 × 108years to transmute 500 g of 135Cs by negative muon beam with the highest intensity currently available.

  2. IAEA activities in the area of partitioning and transmutation

    Science.gov (United States)

    Stanculescu, Alexander

    2006-06-01

    Four major challenges are facing the long-term development of nuclear energy: improvement of the economic competitiveness, meeting increasingly stringent safety requirements, adhering to the criteria of sustainable development, and public acceptance. Meeting the sustainability criteria is the driving force behind the topic of this paper. In this context, sustainability has two aspects: natural resources and waste management. IAEA's activities in the area of Partitioning and Transmutation (P&T) are mostly in response to the latter. While not involving the large quantities of gaseous products and toxic solid wastes associated with fossil fuels, radioactive waste disposal is today's dominant public acceptance issue. In fact, small waste quantities permit a rigorous confinement strategy, and mined geological disposal is the strategy followed by some countries. Nevertheless, political opposition arguing that this does not yet constitute a safe disposal technology has largely stalled these efforts. One of the primary reasons cited is the long life of many of the radioisotopes generated from fission. This concern has led to increased R&D efforts to develop a technology aimed at reducing the amount and radio-toxicity of long-lived radioactive waste through transmutation in fission reactors or sub-critical systems. In the frame of the Project on Technology Advances in Fast Reactors and Accelerator-Driven Systems (ADS), the IAEA initiated a number of activities on utilization of plutonium and transmutation of long-lived radioactive waste, ADS, and deuterium-tritium plasma-driven sub-critical systems. The paper presents past accomplishments, current status and planned activities of this IAEA project.

  3. Measurement of fission cross-section of actinides at n_TOF for advanced nuclear reactors

    CERN Document Server

    Calviani, Marco; Montagnoli, G; Mastinu, P

    2009-01-01

    The subject of this thesis is the determination of high accuracy neutron-induced fission cross-sections of various isotopes - all of which radioactive - of interest for emerging nuclear technologies. The measurements had been performed at the CERN neutron time-of-flight facility n TOF. In particular, in this work, fission cross-sections on 233U, the main fissile isotope of the Th/U fuel cycle, and on the minor actinides 241Am, 243Am and 245Cm have been analyzed. Data on these isotopes are requested for the feasibility study of innovative nuclear systems (ADS and Generation IV reactors) currently being considered for energy production and radioactive waste transmutation. The measurements have been performed with a high performance Fast Ionization Chamber (FIC), in conjunction with an innovative data acquisition system based on Flash-ADCs. The first step in the analysis has been the reconstruction of the digitized signals, in order to extract the information required for the discrimination between fission fragm...

  4. Monte Carlo Modeling of Minor Actinide Burning in Fissile Spallation Targets

    Science.gov (United States)

    Malyshkin, Yury; Pshenichnov, Igor; Mishustin, Igor; Greiner, Walter

    2014-06-01

    Minor actinides (MA) present a harmful part of spent nuclear fuel due to their long half-lives and high radio-toxicity. Neutrons produced in spallation targets of Accelerator Driven Systems (ADS) can be used to transmute and burn MA. Non-fissile targets are commonly considered in ADS design. However, additional neutrons from fission reactions can be used in targets made of fissile materials. We developed a Geant4-based code MCADS (Monte Carlo model for Accelerator Driven Systems) for simulating neutron production and transport in different spallation targets. MCADS is suitable for calculating spatial distributions of neutron flux and energy deposition, neutron multiplication factors and other characteristics of produced neutrons and residual nuclei. Several modifications of the Geant4 source code described in this work were made in order to simulate targets containing MA. Results of MCADS simulations are reported for several cylindrical targets made of U+Am, Am or Am2O3 including more complicated design options with a neutron booster and a reflector. Estimations of Am burning rates are given for the considered cases.

  5. SABR fusion-fission hybrid transmutation reactor design concept

    Science.gov (United States)

    Stacey, Weston

    2009-11-01

    A conceptual design has been developed for a sub-critical advanced burner reactor (SABR) consisting of i) a sodium cooled fast reactor fueled with the transuranics (TRU) from spent nuclear fuel, and ii) a D-T tokamak fusion neutron source based on ITER physics and technology. Subcritical operation enables more efficient transmutation fuel cycles in TRU fueled reactors (without compromising safety), which may be essential for significant reduction in high-level waste repository requirements. ITER will serve as the prototype for the fusion neutron source, which means SABRs could be implemented to help close the nuclear fuel cycle during the 2^nd quarter of the century.

  6. Advanced Techniques for Transmutation Compensation of Extrinsic Silicon Detectors.

    Science.gov (United States)

    1980-10-01

    uniitd ISSPE MENTrbARY NOTES 0 RGRMEEEN.POECTS ReehReactor eutron .2F 22320 extrmaofsico elLria paaeesa ucinoline AFre ceivt Wihtgnet Acoast a function...11V 34. Comparison of the effects of various fast-to- thermal neutron ratios ... .... ............. 120 35. Comparison of isochronal annealing...isotopes, 0 Si(relati%’e abundance of 3"), as a resul t of thermal neutron capture and beta decay, is thc only isotope to be transmuted into an impurity

  7. BCS as Foundation and Inspiration: the Transmutation of Symmetry

    Science.gov (United States)

    Wilczek, Frank

    The BCS theory injected two powerful ideas into the collective consciousness of theoretical physics: pairing and spontaneous symmetry breaking. In the 50 years since the seminal work of Bardeen, Cooper and Schrieffer, those ideas have found important use in areas quite remote from the stem application to metallic superconductivity. This is a brief and eclectic sketch of some highlights, emphasizing relatively recent developments in QCD and in the theory of quantum statistics, and including a few thoughts about future directions. A common theme is the importance of symmetry transmutation, as opposed to the simple breaking of electromagnetic U(1) symmetry in classic metallic superconductors.

  8. Retrieval system of nuclear data for transmutation of nuclear materials

    Energy Technology Data Exchange (ETDEWEB)

    Fujita, Mitsutane; Utsumi, Misako; Noda, Tetsuji [National Research Inst. for Metals, Tsukuba, Ibaraki (Japan)

    1997-03-01

    A database storing the data on nuclear reaction was built to calculate for simulating transmutation behaviours of materials /1/-/3/. In order to retrieve and maintain the database, the user interface for the data retrieval was developed where special knowledge on handling of the database or the machine structure is not required for end-user. It is indicated that using the database, the possibility of He formation and radioactivity in a material can be easily retrieved though the evaluation is qualitatively. (author)

  9. Electrorecovery of actinides at room temperature

    Energy Technology Data Exchange (ETDEWEB)

    Stoll, Michael E [Los Alamos National Laboratory; Oldham, Warren J [Los Alamos National Laboratory; Costa, David A [Los Alamos National Laboratory

    2008-01-01

    There are a large number of purification and processing operations involving actinide species that rely on high-temperature molten salts as the solvent medium. One such application is the electrorefining of impure actinide metals to provide high purity material for subsequent applications. There are some drawbacks to the electrodeposition of actinides in molten salts including relatively low yields, lack of accurate potential control, maintaining efficiency in a highly corrosive environment, and failed runs. With these issues in mind we have been investigating the electrodeposition of actinide metals, mainly uranium, from room temperature ionic liquids (RTILs) and relatively high-boiling organic solvents. The RTILs we have focused on are comprised of 1,3-dialkylimidazolium or quaternary ammonium cations and mainly the {sup -}N(SO{sub 2}CF{sub 3}){sub 2} anion [bis(trif1uoromethylsulfonyl)imide {equivalent_to} {sup -}NTf{sub 2}]. These materials represent a class of solvents that possess great potential for use in applications employing electrochemical procedures. In order to ascertain the feasibility of using RTILs for bulk electrodeposition of actinide metals our research team has been exploring the electron transfer behavior of simple coordination complexes of uranium dissolved in the RTIL solutions. More recently we have begun some fundamental electrochemical studies on the behavior of uranium and plutonium complexes in the organic solvents N-methylpyrrolidone (NMP) and dimethylsulfoxide (DMSO). Our most recent results concerning electrodeposition will be presented in this account. The electrochemical behavior of U(IV) and U(III) species in RTILs and the relatively low vapor pressure solvents NMP and DMSO is described. These studies have been ongoing in our laboratory to uncover conditions that will lead to the successful bulk electrodeposition of actinide metals at a working electrode surface at room temperature or slightly elevated temperatures. The RTILs we

  10. Recovery of actinides from actinide-aluminium alloys by chlorination: Part I

    Science.gov (United States)

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

    2011-07-01

    Pyrochemical processes in molten LiCl-KCl are being developed in ITU for recovery of actinides from spent nuclear fuel. The fuel is anodically dissolved to the molten salt electrolyte and actinides are electrochemically reduced on solid aluminium cathodes forming solid actinide-aluminium alloys. A chlorination route is being investigated for recovery of actinides from the alloys. This route consists in three steps: Vacuum distillation for removal of the salt adhered on the electrode, chlorination of the actinide-aluminium alloys by chlorine gas and sublimation of the formed AlCl 3. A thermochemical study showed thermodynamic feasibility of all three steps. On the basis of the conditions identified by the calculations, experiments using pure UAl 3 alloy were carried out to evaluate and optimise the chlorination step. The work was focused on determination of the optimal temperature and Cl 2/UAl 3 molar ratio, providing complete chlorination of the alloy without formation of volatile UCl 5 and UCl 6. The results showed high efficient chlorination at a temperature of 150 °C.

  11. Microbial Transformations of Actinides and Other Radionuclides

    Energy Technology Data Exchange (ETDEWEB)

    Francis,A.J.; Dodge, C. J.

    2009-01-07

    Microorganisms can affect the stability and mobility of the actinides and other radionuclides released from nuclear fuel cycle and from nuclear fuel reprocessing plants. Under appropriate conditions, microorganisms can alter the chemical speciation, solubility and sorption properties and thus could increase or decrease the concentrations of radionuclides in solution in the environment and the bioavailability. Dissolution or immobilization of radionuclides is brought about by direct enzymatic action or indirect non-enzymatic action of microorganisms. Although the physical, chemical, and geochemical processes affecting dissolution, precipitation, and mobilization of radionuclides have been extensively investigated, we have only limited information on the effects of microbial processes and biochemical mechanisms which affect the stability and mobility of radionuclides. The mechanisms of microbial transformations of the major and minor actinides U, Pu, Cm, Am, Np, the fission products and other radionuclides such as Ra, Tc, I, Cs, Sr, under aerobic and anaerobic conditions in the presence of electron donors and acceptors are reviewed.

  12. Seventeen-coordinate actinide helium complexes

    Energy Technology Data Exchange (ETDEWEB)

    Kaltsoyannis, Nikolas [School of Chemistry, The University of Manchester (United Kingdom)

    2017-06-12

    The geometries and electronic structures of molecular ions featuring He atoms complexed to actinide cations are explored computationally using density functional and coupled cluster theories. A new record coordination number is established, as AcHe{sub 17}{sup 3+}, ThHe{sub 17}{sup 4+}, and PaHe{sub 17}{sup 4+} are all found to be true geometric minima, with the He atoms clearly located in the first shell around the actinide. Analysis of AcHe{sub n}{sup 3+} (n=1-17) using the quantum theory of atoms in molecules (QTAIM) confirms these systems as having closed shell, charge-induced dipole bonding. Excellent correlations (R{sup 2}>0.95) are found between QTAIM metrics (bond critical point electron densities and delocalization indices) and the average Ac-He distances, and also with the incremental He binding energies. (copyright 2017 Wiley-VCH Verlag GmbH and Co. KGaA, Weinheim)

  13. Practising alchemy: the transmutation of evidence into best health care.

    Science.gov (United States)

    Goodyear-Smith, Felicity

    2011-04-01

    Alchemy was the synthesis or transmutation of all elements in perfect balance to obtain the philosopher's stone, the key to health. Just as alchemists sought this, so health practitioners always seek the best possible practice for optimal health outcomes for our patients. Best practice requires full knowledge--a little information can be dangerous. We need to serve our apprenticeship before we master our profession. Our profession is about improving health care. While the journey may start at medical school, the learning never ceases. It is not only about practising medicine, it is about the development of the practitioner. Professional practice requires systematic thinking combined with capacity to deal morally and creatively in areas of complexity and uncertainty appropriate to a specific context. It requires exemplary communication skills to interact with patients to facilitate collaborative decision making resulting in best practice. The synthesis of scientific and contextual evidence is a concept which applies to all disciplines where theoretical knowledge needs to be transferred to action to inform best practice. Decisions need to be made which take into account a complex array of factors, such as social and legal issues and resource constraints. Therefore, journey towards best practice involves transmutation of these three elements: scientific knowledge, the context in which it is applied and phronesis, the practical wisdom of the practitioner. All science has its limitations and we can never know all possible contextual information. Hence, like the philosopher's stone, best practice is a goal to which we aspire but never quite attain.

  14. Neutron data experiments for transmutation. Annual Report 2006/2007

    Energy Technology Data Exchange (ETDEWEB)

    Blomgren, J.; Andersson, P.; Bevilacqua, R.; Nilsson, L.; Pomp, S.; Simutkin, V.; Oehrn, A.; Oesterlund, M. (Uppsala Univ. (SE). Dept. of Neutron Research)

    2007-10-15

    The project NEXT, Neutron data Experiments for Transmutation, is performed within the nuclear reactions group of the Department of Neutron Research, Uppsala University. The activities of the group are directed towards experimental studies of nuclear reaction probabilities of importance for various applications, like transmutation of nuclear waste, biomedical effects and electronics reliability. The experimental work is primarily undertaken at the The Svedberg Laboratory (TSL) in Uppsala, where the group is operating two world-unique instruments, MEDLEY and SCANDAL. Highlights from the past year: The TSL neutron beam facility and the MEDLEY detector system have been upgraded. Funding for a major upgrade of the SCANDAL facility has been approved, and practical work has been initiated. Three new PhD students have been accepted. The Uppsala group contributed twelve accepted publications at the International Conference on Nuclear Data for Science and Technology, Nice, France, April 22-27, 2007. The EU project CANDIDE (Coordination Action on Nuclear Data for Industrial Development in Europe), coordinated by Jan Blomgren, started January 1, 2007. The EU project EFNUDAT (European Facilities for Nuclear Data research), partly coordinated by Jan Blomgren, started November 1, 2006. Nuclear power education has reached all-time high at Uppsala University. A contract with KSU (Nuclear Training and Safety Centre) on financing the increased volume of teaching for industry needs has been signed

  15. Preparation, properties, and some recent studies of the actinide metals

    Energy Technology Data Exchange (ETDEWEB)

    Haire, R.G.

    1985-01-01

    The actinide elements form a unique series of metals. The variation in their physial properties combined with the varying availability of the different elements offers a challenge to the preparative scientist. This article provides a brief review of selected methods used for preparing ..mu..g to kg amounts of the actinide metals and the properties of these metals. In addition, some recent studies on selected actinide metals are discussed. 62 refs.

  16. Positron Spectroscopy of Hydrothermally Grown Actinide Oxides

    Science.gov (United States)

    2014-03-27

    In this method, the powdered material is placed in a solution which contains extremely powerful mineralizers , such as cesium fluoride for actinide...environmentally triggered background counts and it subtends a very small solid angle with respect to the detector. Thus, the benefit of the lead sheet outweighs...low electron density. This is mainly a property of their atomic makeup , though the microstructure of the paper is porous as well. In addition, a

  17. Conceptual design of minor actinides burner with an accelerator-driven subcritical system.

    Energy Technology Data Exchange (ETDEWEB)

    Cao, Y.; Gohar, Y. (Nuclear Engineering Division)

    2011-11-04

    systems consume about 1.2 tons of actinides per year and produce 3 GW thermal power, with a proton beam power of 25 MW. Total MA fuel that would be consumed in the first 10 years of operation is 9.85, 11.80, or 12.68 tons, respectively, for the systems with 5, 7, or 10% actinide fuel particles loaded in the LBE. The corresponding annual MA fuel transmutation rate after reaching equilibrium at 10 years of operation is 0.83, 0.94, or 1.02 tons/year, respectively. Assuming that the ADS systems can be operated for 35 full-power years, the total MAs consumed in the three ADS systems are 30.6, 35.3, and 37.2 tons, respectively. For the three configurations, it is estimated that 3.8, 3.3, or 3.1 ADS system units are required to utilize the entire 115 tons of MA fuel in the SNF inventory, respectively.

  18. Actinide and lanthanide separation process (ALSEP)

    Science.gov (United States)

    Guelis, Artem V.

    2013-01-15

    The process of the invention is the separation of minor actinides from lanthanides in a fluid mixture comprising, fission products, lanthanides, minor actinides, rare earth elements, nitric acid and water by addition of an organic chelating aid to the fluid; extracting the fluid with a solvent comprising a first extractant, a second extractant and an organic diluent to form an organic extractant stream and an aqueous raffinate. Scrubbing the organic stream with a dicarboxylic acid and a chelating agent to form a scrubber discharge. The scrubber discharge is stripped with a simple buffering agent and a second chelating agent in the pH range of 2.5 to 6.1 to produce actinide and lanthanide streams and spent organic diluents. The first extractant is selected from bis(2-ethylhexyl)hydrogen phosphate (HDEHP) and mono(2-ethylhexyl)2-ethylhexyl phosphonate (HEH(EHP)) and the second extractant is selected from N,N,N,N-tetra-2-ethylhexyl diglycol amide (TEHDGA) and N,N,N',N'-tetraoctyl-3-oxapentanediamide (TODGA).

  19. Recovery of actinides from actinide-aluminium alloys by chlorination: Part II

    Science.gov (United States)

    Souček, P.; Cassayre, L.; Eloirdi, R.; Malmbeck, R.; Meier, R.; Nourry, C.; Claux, B.; Glatz, J.-P.

    2014-04-01

    A chlorination route is being investigated for recovery of actinides from actinide-aluminium alloys, which originate from pyrochemical recovery of actinides from spent metallic nuclear fuel by electrochemical methods in molten LiCl-KCl. In the present work, the most important steps of this route were experimentally tested using U-Pu-Al alloy prepared by electrodeposition of U and Pu on solid aluminium plate electrodes. The investigated processes were vacuum distillation for removal of the salt adhered on the electrode, chlorination of the alloy by chlorine gas and sublimation of the AlCl3 formed. The processes parameters were set on the base of a previous thermochemical study and an experimental work using pure UAl3 alloy. The present experimental results indicated high efficiency of salt distillation and chlorination steps, while the sublimation step should be further optimised.

  20. Hydrothermal decomposition of actinide(IV oxalates: a new aqueous route towards reactive actinide oxide nanocrystals

    Directory of Open Access Journals (Sweden)

    Walter Olaf

    2016-01-01

    Full Text Available The hydrothermal decomposition of actinide(IV oxalates (An= Th, U, Pu at temperatures between 95 and 250 °C is shown to lead to the production of highly crystalline, reactive actinide oxide nanocrystals (NCs. This aqueous process proved to be quantitative, reproducible and fast (depending on temperature. The NCs obtained were characterised by X-ray diffraction and TEM showing their size to be smaller than 15 nm. Attempts to extend this general approach towards transition metal or lanthanide oxalates failed in the 95–250 °C temperature range. The hydrothermal decomposition of actinide oxalates is therefore a clean, flexible and powerful approach towards NCs of AnO2 with possible scale-up potential.

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

    Science.gov (United States)

    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%).

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

    Energy Technology Data Exchange (ETDEWEB)

    Apse, V. A.; Kulikov, G. G., E-mail: ggkulikov@mephi.ru; Kulikov, E. G. [National Research Nuclear University MEPhI (Moscow Engineering Physics Institute) (Russian Federation)

    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%).

  3. Transmutation technology development; a comparative study on the fuel loading flexibility between critical and subcritical reactors for TRU transmutation

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Jong Kyung; Lee, J. K.; Han, C. Y.; Shin, C. H.; Park, S. H.; Kim, K. H. [Hanyang University, Seoul (Korea)

    2001-04-01

    A comparative analysis of the nuclear characteristics between the critical and the subcritical cores was performed, focused on the fuel loading flexibility as a preliminary study to set up the optimal concept for TRU transmutation. This study made efforts to compare the variation tendency of neutron spectrum and dynamics parameters against various recovery factors of uranium and lanthanides such as the fuel temperature coefficient, the coolant temperature coefficient, the effective delayed neutron fraction, and the effective neutron generation time. The intrinsic differences in nuclear characteristics due to the different fuel loading concentration between both cores were analyzed. At the same time, effects of external neutron source on the subcritical core characteristics and the role of neutron absorber in critical reactors were evaluated. From the analyses of results, some useful information were generated, which can be employed to design optimization study aiming at the more flexibility through minimization of the nuclear characteristics sensitivity to fuel composition of TRU transmutation reactor. Finally, comparative conclusions in the fuel loading flexibility were derived from the analysis results performed in this study, based on the difference in the nuclear characteristics sensitivity to the fuel composition between both concepts. 19 refs., 39 figs., 45 tabs. (Author)

  4. New density functional theory approaches for enabling prediction of chemical and physical properties of plutonium and other actinides.

    Energy Technology Data Exchange (ETDEWEB)

    Mattsson, Ann Elisabet

    2012-01-01

    Density Functional Theory (DFT) based Equation of State (EOS) construction is a prominent part of Sandia's capabilities to support engineering sciences. This capability is based on amending experimental data with information gained from computational investigations, in parts of the phase space where experimental data is hard, dangerous, or expensive to obtain. A prominent materials area where such computational investigations are hard to perform today because of limited accuracy is actinide and lanthanide materials. The Science of Extreme Environment Lab Directed Research and Development project described in this Report has had the aim to cure this accuracy problem. We have focused on the two major factors which would allow for accurate computational investigations of actinide and lanthanide materials: (1) The fully relativistic treatment needed for materials containing heavy atoms, and (2) the needed improved performance of DFT exchange-correlation functionals. We have implemented a fully relativistic treatment based on the Dirac Equation into the LANL code RSPt and we have shown that such a treatment is imperative when calculating properties of materials containing actinides and/or lanthanides. The present standard treatment that only includes some of the relativistic terms is not accurate enough and can even give misleading results. Compared to calculations previously considered state of the art, the Dirac treatment gives a substantial change in equilibrium volume predictions for materials with large spin-orbit coupling. For actinide and lanthanide materials, a Dirac treatment is thus a fundamental requirement in any computational investigation, including those for DFT-based EOS construction. For a full capability, a DFT functional capable of describing strongly correlated systems such as actinide materials need to be developed. Using the previously successful subsystem functional scheme developed by Mattsson et.al., we have created such a functional. In

  5. New density functional theory approaches for enabling prediction of chemical and physical properties of plutonium and other actinides.

    Energy Technology Data Exchange (ETDEWEB)

    Mattsson, Ann Elisabet

    2012-01-01

    Density Functional Theory (DFT) based Equation of State (EOS) construction is a prominent part of Sandia's capabilities to support engineering sciences. This capability is based on amending experimental data with information gained from computational investigations, in parts of the phase space where experimental data is hard, dangerous, or expensive to obtain. A prominent materials area where such computational investigations are hard to perform today because of limited accuracy is actinide and lanthanide materials. The Science of Extreme Environment Lab Directed Research and Development project described in this Report has had the aim to cure this accuracy problem. We have focused on the two major factors which would allow for accurate computational investigations of actinide and lanthanide materials: (1) The fully relativistic treatment needed for materials containing heavy atoms, and (2) the needed improved performance of DFT exchange-correlation functionals. We have implemented a fully relativistic treatment based on the Dirac Equation into the LANL code RSPt and we have shown that such a treatment is imperative when calculating properties of materials containing actinides and/or lanthanides. The present standard treatment that only includes some of the relativistic terms is not accurate enough and can even give misleading results. Compared to calculations previously considered state of the art, the Dirac treatment gives a substantial change in equilibrium volume predictions for materials with large spin-orbit coupling. For actinide and lanthanide materials, a Dirac treatment is thus a fundamental requirement in any computational investigation, including those for DFT-based EOS construction. For a full capability, a DFT functional capable of describing strongly correlated systems such as actinide materials need to be developed. Using the previously successful subsystem functional scheme developed by Mattsson et.al., we have created such a functional. In

  6. Experimental demonstration of free-space optical vortex transmutation with polygonal lenses.

    Science.gov (United States)

    Gao, Nan; Xie, Changqing

    2012-08-01

    Vortex transmutation was predicted to take place when vortices interact with systems possessing discrete rotational symmetries of finite order [Phys. Rev. Lett.95, 123901 (2005)]. Here we report what is believed to be the first experimental demonstration of vortex transmutation. We show that in free space, by simply inserting polygonal lenses into the optical path, the central vorticity of a coaxially incident optical vortex can be changed following the modular transmutation rule. We generate the wavefront at the exit face of the lenses with computer generated holograms and measure the output vorticity using the interference patterns at the focal plane. The results agree well with theoretical predictions.

  7. An improved transmutation method for quantitative determination of the components in multicomponent overlapping chromatograms.

    Science.gov (United States)

    Shao, Xueguang; Yu, Zhengliang; Ma, Chaoxiong

    2004-06-01

    An improved method is proposed for the quantitative determination of multicomponent overlapping chromatograms based on a known transmutation method. To overcome the main limitation of the transmutation method caused by the oscillation generated in the transmutation process, two techniques--wavelet transform smoothing and the cubic spline interpolation for reducing data points--were adopted, and a new criterion was also developed. By using the proposed algorithm, the oscillation can be suppressed effectively, and quantitative determination of the components in both the simulated and experimental overlapping chromatograms is successfully obtained.

  8. Accelerator transmutation studies at Los Alamos with LAHET, MCNP, and CINDER`90

    Energy Technology Data Exchange (ETDEWEB)

    Wilson, W.B.; England, T.R.; Arthur, E.D. [and others

    1993-09-01

    Versions of the CINDER code have been used over three decades for determination of reactor fuel inventories and aggregate neutron absorption and radioactive decay properties. The CINDER`90 code, an evolving version which requires no predetermined nuclide chain structure, is suitable for a wider range of transmutation problems including those treated with older versions. In recent accelerator transmutation studies, the CINDER`90 code has been linked with the LAHET Code System (LCS) and, for high-energy calculations, with SUPERHET. A description of the nature of these linked calculational tools is given; data requirements for the transmutation studies are described; and, examples of linked calculations are described for some interesting accelerator applications.

  9. An omnidirectional retroreflector based on the transmutation of dielectric singularities.

    Science.gov (United States)

    Ma, Yun Gui; Ong, C K; Tyc, Tomás; Leonhardt, Ulf

    2009-08-01

    Transformation optics is a concept used in some metamaterials to guide light on a predetermined path. In this approach, the materials implement coordinate transformations on electromagnetic waves to create the illusion that the waves are propagating through a virtual space. Transforming space by appropriately designed materials makes devices possible that have been deemed impossible. In particular, transformation optics has led to the demonstration of invisibility cloaking for microwaves, surface plasmons and infrared light. Here, on the basis of transformation optics, we implement a microwave device that would normally require a dielectric singularity, an infinity in the refractive index. To fabricate such a device, we transmute a dielectric singularity in virtual space into a mere topological defect in a real metamaterial. In particular, we demonstrate an omnidirectional retroreflector, a device for faithfully reflecting images and for creating high visibility from all directions. Our method is robust, potentially broadband and could also be applied to visible light using similar techniques.

  10. From teosinte to maize: the catastrophic sexual transmutation.

    Science.gov (United States)

    Iltis, H H

    1983-11-25

    An alternative to the theory that the ear of maize (Zea mays ssp. mays) evolved from a slender female ear of a Mexican annual teosinte holds that it was derived from the central spike of a male teosinte inflorescence (tassel) which terminates the primary lateral branches. This alternative hypothesis is more consistent with morphology and explains the anomalous lack of significant genetic and biochemical differences between these taxa. Maize, the only cereal with unisexual inflorescences, evolved through a sudden epigenetic sexual transmutation involving condensation of primary branches, which brought their tassels into the zone of female expression, leading to strong apical dominance and a catastrophic shift in nutrient allocation. Initially, this quantum change may have involved no new mutations, but rather genetic assimilation under human selection of an abnormality, perhaps environmentally triggered.

  11. An omnidirectional retroreflector based on the transmutation of dielectric singularities

    CERN Document Server

    Ma, Yun Gui; Tyc, Tomas; Leonhardt, Ulf

    2009-01-01

    In the field of transformation optics, metamaterials mimic the effect of coordinate transformations on electromagnetic waves, creating the illusion that the waves are propagating through a virtual space. Transforming space by appropriately designed materials makes devices possible that have been deemed impossible. In particular, transformation optics has led to the demonstration of invisibility cloaking for microwaves, surface plasmons and infrared light. Here we report the achievement of another "impossible task". We implement, for microwaves, a device that would normally require a dielectric singularity, an infinity in the refractive index. We transmute a singularity in virtual space into a mere topological defect in a real metamaterial. In particular, we demonstrate an omnidirectional retroreflector, a device for faithfully reflecting images and for creating high visibility, from all directions. Our method is robust, potentially broadband and similar techniques could be applied for visible light.

  12. The physics design of accelerator-driven transmutation systems

    Energy Technology Data Exchange (ETDEWEB)

    Venneri, F.

    1995-02-01

    Nuclear systems under study in the Los Alamos Accelerator-Driven Transmutation Technology program (ADTT) will allow the destruction of nuclear spent fuel and weapons-return plutonium, as well as the production of nuclear energy from the thorium cycle, without a long-lived radioactive waste stream. The subcritical systems proposed represent a radical departure from traditional nuclear concepts (reactors), yet the actual implementation of ADTT systems is based on modest extrapolations of existing technology. These systems strive to keep the best that the nuclear technology has developed over the years, within a sensible conservative design envelope and eventually manage to offer a safer, less expensive and more environmentally sound approach to nuclear power.

  13. Transmutation Scheme of Coin Flipping Protocol and Utilization

    Institute of Scientific and Technical Information of China (English)

    XIE Yumin; MING Yang; SHI Feng; MUHAMMAD Kamran

    2006-01-01

    Coin flipping by telephone protocol(CFP) is utilized in a system to exchange a binary sequence at random between two person apart far from each other. However, CFP cannot be used in a system with many users like in a group environment system. A transmutation of CFP named T-CFP is proposed in this paper. The precondition of T-CFP is the system's user trusts the system center and center's cheating is meaningless at the same time. The significant difference between CFP and T-CFP is that CFP supports only two users while T-CFP can support many users to exchange special information. The security and efficiency of T-CFP are discussed with a detailed example on T-CFP utilization is demonstrated in this paper.

  14. Neutron data experiments for transmutation. Annual Report 2007/2008

    Energy Technology Data Exchange (ETDEWEB)

    Blomgren, J.; al-Adili, A.; Andersson, P.; Bevilacqua, R.; Nilsson, L.; Pomp, S.; Simutkin, V.; Oehrn, A.; Oesterlund, M. (Uppsala Univ. (Sweden). Div. of Applied Nuclear Physics)

    2008-08-15

    The project NEXT, Neutron data Experiments for Transmutation, is performed within the nuclear reactions group of the Dept. of Physics and Astronomy. The activities of the group are directed towards experimental studies of nuclear reaction probabilities of importance for various applications, like transmutation of nuclear waste, biomedical effects and electronics reliability. The experimental work is primarily undertaken at the The Svedberg Laboratory (TSL) in Uppsala, where the group is operating two world-unique instruments, MEDLEY and SCANDAL. Highlights from the past year: - The SCANDAL facility has been upgraded. - One PhD student has successfully defended her thesis. - Two PhD students have been accepted. - Vasily Simutkin has been selected as one of the top 12 PhD students within the European Nuclear Education Network. He has accordingly been invited to present his work at the ENEN PhD event held in connection with the PHYSOR conference in Interlaken, Switzerland, September 2008. - A research collaboration with the dedicated EU laboratory for nuclear data research has been established. - A well-attended workshop on nuclear data for ADS and Gen-IV has been organized as part of the EU project CANDIDE (Coordination Action on Nuclear Data for Industrial Development in Europe), coordinated by Jan Blomgren. - Several experiments have been performed at TSL, with beamtime funded through the EU project EFNUDAT (European Facilities for Nuclear Data research), partly coordinated by Jan Blomgren. - Nuclear power education has reached all-time high at Uppsala University. In particular, industry education has increased significantly. - IAEA has visited Uppsala University to investigate the industry-related nuclear power education, as part of a safety culture review of the Forsmark nuclear power plant

  15. Capability Paternalism

    NARCIS (Netherlands)

    Claassen, R.J.G.

    2014-01-01

    A capability approach prescribes paternalist government actions to the extent that it requires the promotion of specific functionings, instead of the corresponding capabilities. Capability theorists have argued that their theories do not have much of these paternalist implications, since promoting c

  16. Research in actinide chemistry. Progress report, 1990--1993

    Energy Technology Data Exchange (ETDEWEB)

    Choppin, G.R.

    1993-04-01

    This research studies the behavior of the actinide elements in aqueous solution. The high radioactivity of the transuranium actinides limits the concentrations which can be studied and, consequently, limits the experimental techniques. However, oxidation state analogs (trivalent lanthanides, tetravalent thorium, and hexavalent uranium) do not suffer from these limitations. Behavior of actinides in the environment are a major USDOE concern, whether in connection with long-term releases from a repository, releases from stored defense wastes or accidental releases in reprocessing, etc. Principal goal of our research was expand the thermodynamic data base on complexation of actinides by natural ligands (e.g., OH{sup {minus}}, CO{sub 3}{sup 2{minus}}, PO{sub 4}{sup 3{minus}}, humates). The research undertakes fundamental studies of actinide complexes which can increase understanding of the environmental behavior of these elements.

  17. Chemistry of lower valent actinide halides

    Energy Technology Data Exchange (ETDEWEB)

    Lau, K.H.; Hildenbrand, D.L.

    1992-01-01

    This research effort was concerned almost entirely with the first two members of the actinide series, thorium and uranium, although the work was later extended to some aspects of the neptunium-fluorine system in a collaborative program with Los Alamos National Laboratory. Detailed information about the lighter actinides will be helpful in modeling the properties of the heavier actinide compounds, which will be much more difficult to study experimentally. In this program, thermochemical information was obtained from high temperature equilibrium measurements made by effusion-beam mass spectrometry and by effusion-pressure techniques. Data were derived primarily from second-law analysis so as to avoid potential errors in third-law calculations resulting from uncertainties in spectroscopic and molecular constants. This approach has the additional advantage of yielding reaction entropies that can be checked for consistency with various molecular constant assignments for the species involved. In the U-F, U-Cl, and U-Br systems, all of the gaseous species UX, UX{sub 2}, UX{sub 3}, UX{sub 4}, and UX{sub 5}, where X represents the halogen, were identified and characterized; the corresponding species ThX, ThX{sub 2}, ThX{sub 3}, and ThX{sub 4} were studied in the Th-F, Th-Cl, and Th-Br systems. A number of oxyhalide species in the systems U-0-F, U-0-Cl, Th-0-F, and Th-O-Cl were studied thermochemically. Additionally, the sublimation thermodynamics of NpF{sub 4}(s) and NpO{sub 2}F{sub 2}(s) were studied by mass spectrometry.

  18. JOWOG 22/2 - Actinide Chemical Technology (July 9-13, 2012)

    Energy Technology Data Exchange (ETDEWEB)

    Jackson, Jay M. [Los Alamos National Laboratory; Lopez, Jacquelyn C. [Los Alamos National Laboratory; Wayne, David M. [Los Alamos National Laboratory; Schulte, Louis D. [Los Alamos National Laboratory; Finstad, Casey C. [Los Alamos National Laboratory; Stroud, Mary Ann [Los Alamos National Laboratory; Mulford, Roberta Nancy [Los Alamos National Laboratory; MacDonald, John M. [Los Alamos National Laboratory; Turner, Cameron J. [Los Alamos National Laboratory; Lee, Sonya M. [Los Alamos National Laboratory

    2012-07-05

    The Plutonium Science and Manufacturing Directorate provides world-class, safe, secure, and reliable special nuclear material research, process development, technology demonstration, and manufacturing capabilities that support the nation's defense, energy, and environmental needs. We safely and efficiently process plutonium, uranium, and other actinide materials to meet national program requirements, while expanding the scientific and engineering basis of nuclear weapons-based manufacturing, and while producing the next generation of nuclear engineers and scientists. Actinide Process Chemistry (NCO-2) safely and efficiently processes plutonium and other actinide compounds to meet the nation's nuclear defense program needs. All of our processing activities are done in a world class and highly regulated nuclear facility. NCO-2's plutonium processing activities consist of direct oxide reduction, metal chlorination, americium extraction, and electrorefining. In addition, NCO-2 uses hydrochloric and nitric acid dissolutions for both plutonium processing and reduction of hazardous components in the waste streams. Finally, NCO-2 is a key team member in the processing of plutonium oxide from disassembled pits and the subsequent stabilization of plutonium oxide for safe and stable long-term storage.

  19. Fission cross section measurements for minor actinides

    Energy Technology Data Exchange (ETDEWEB)

    Fursov, B. [IPPE, Obninsk (Russian Federation)

    1997-03-01

    The main task of this work is the measurement of fast neutron induced fission cross section for minor actinides of {sup 238}Pu, {sup 242m}Am, {sup 243,244,245,246,247,248}Cm. The task of the work is to increase the accuracy of data in MeV energy region. Basic experimental method, fissile samples, fission detectors and electronics, track detectors, alpha counting, neutron generation, fission rate measurement, corrections to the data and error analysis are presented in this paper. (author)

  20. Calculated Bulk Properties of the Actinide Metals

    DEFF Research Database (Denmark)

    Skriver, Hans Lomholt; Andersen, O. K.; Johansson, B.

    1978-01-01

    Self-consistent relativistic calculations of the electronic properties for seven actinides (Ac-Am) have been performed using the linear muffin-tin orbitals method within the atomic-sphere approximation. Exchange and correlation were included in the local spin-density scheme. The theory explains...... the variation of the atomic volume and the bulk modulus through the 5f series in terms of an increasing 5f binding up to plutonium followed by a sudden localisation (through complete spin polarisation) in americium...

  1. Electronic structure and magnetism in actinide compounds

    Energy Technology Data Exchange (ETDEWEB)

    Durakiewicz, T. [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States)]. E-mail: tomasz@lanl.gov; Joyce, J.J. [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Lander, G.H. [JRC, Institute of Transuranium Elements, Postfach 2340, 76125 Karlsruhe (Germany); Olson, C.G. [Ames Laboratory, Iowa State University, Ames, Iowa 5011 (United States); Butterfield, M.T. [Lawrence Livermoore National Laboratory, Livermoore, CA 94550 (United States); Guziewicz, E. [Institute of Physics, Polish Academy of Sciences, 02-668 Warsaw (Poland); Batista, C.D. [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Arko, A.J. [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Morales, L. [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Mattenberger, K. [Laboratorium fur Festkorperphysik, ETH, CH-8093, Zurich (Switzerland); Vogt, O. [Laboratorium fur Festkorperphysik, ETH, CH-8093, Zurich (Switzerland)

    2006-05-01

    A close relationship between electronic structure and magnetic properties is observed in actinide compounds. The exact nature of this relationship is under investigation. We present examples of a direct link between electronic structure and ordered magnetic moment and/or magnetization. Specifically, results obtained for cubic U, Np and Pu compounds and quasi-2D U compounds are be presented. In the case of cubic compounds, a direct relationship between binding energy of valence band features and magnetic moment will be discussed. A Stoner-like mechanism and simple mean-field explanation is proposed for ferromagnetic UTe.

  2. Calculated Bulk Properties of the Actinide Metals

    DEFF Research Database (Denmark)

    Skriver, Hans Lomholt; Andersen, O. K.; Johansson, B.

    1978-01-01

    Self-consistent relativistic calculations of the electronic properties for seven actinides (Ac-Am) have been performed using the linear muffin-tin orbitals method within the atomic-sphere approximation. Exchange and correlation were included in the local spin-density scheme. The theory explains t...... the variation of the atomic volume and the bulk modulus through the 5f series in terms of an increasing 5f binding up to plutonium followed by a sudden localisation (through complete spin polarisation) in americium...

  3. Fission cross section measurements for minor actinides

    Energy Technology Data Exchange (ETDEWEB)

    Fursov, B. [IPPE, Obninsk (Russian Federation)

    1997-03-01

    The main task of this work is the measurement of fast neutron induced fission cross section for minor actinides of {sup 238}Pu, {sup 242m}Am, {sup 243,244,245,246,247,248}Cm. The task of the work is to increase the accuracy of data in MeV energy region. Basic experimental method, fissile samples, fission detectors and electronics, track detectors, alpha counting, neutron generation, fission rate measurement, corrections to the data and error analysis are presented in this paper. (author)

  4. Reducing Actinide Production Using Inert Matrix Fuels

    Energy Technology Data Exchange (ETDEWEB)

    Deinert, Mark [Colorado School of Mines, Golden, CO (United States)

    2017-08-23

    The environmental and geopolitical problems that surround nuclear power stem largely from the longlived transuranic isotopes of Am, Cm, Np and Pu that are contained in spent nuclear fuel. New methods for transmuting these elements into more benign forms are needed. Current research efforts focus largely on the development of fast burner reactors, because it has been shown that they could dramatically reduce the accumulation of transuranics. However, despite five decades of effort, fast reactors have yet to achieve industrial viability. A critical limitation to this, and other such strategies, is that they require a type of spent fuel reprocessing that can efficiently separate all of the transuranics from the fission products with which they are mixed. Unfortunately, the technology for doing this on an industrial scale is still in development. In this project, we explore a strategy for transmutation that can be deployed using existing, current generation reactors and reprocessing systems. We show that use of an inert matrix fuel to recycle transuranics in a conventional pressurized water reactor could reduce overall production of these materials by an amount that is similar to what is achievable using proposed fast reactor cycles. Furthermore, we show that these transuranic reductions can be achieved even if the fission products are carried into the inert matrix fuel along with the transuranics, bypassing the critical separations hurdle described above. The implications of these findings are significant, because they imply that inert matrix fuel could be made directly from the material streams produced by the commercially available PUREX process. Zirconium dioxide would be an ideal choice of inert matrix in this context because it is known to form a stable solid solution with both fission products and transuranics.

  5. Transmutation of 129I, 237Np, 238Pu, 239Pu, and 241Am using neutrons produced in target-blanket system `Energy plus Transmutation' by relativistic protons

    Indian Academy of Sciences (India)

    J Adam; K Katovsky; A Balabekyan; V G Kalinnikov; M I Krivopustov; H Kumawat; A A Solnyshkin; V I Stegailov; S G Stetsenko; V M Tsoupko-Sitnikov; W Westmeier

    2007-02-01

    Target-blanket facility `Energy + Transmutation' was irradiated by proton beam extracted from the Nuclotron Accelerator in Laboratory of High Energies of Joint Institute for Nuclear Research in Dubna, Russia. Neutrons generated by the spallation reactions of 0.7, 1.0, 1.5 and 2 GeV protons and lead target interact with subcritical uranium blanket. In the neutron field outside the blanket, radioactive iodine, neptunium, plutonium and americium samples were irradiated and transmutation reaction yields (residual nuclei production yields) have been determined using -spectroscopy. Neutron field's energy distribution has also been studied using a set of threshold detectors. Results of transmutation studies of 129I, 237Np, 238Pu, 239Pu and 241Am are presented.

  6. Partitioning and transmutation. Current developments - 2004. A report from the Swedish reference group on P and T-research

    Energy Technology Data Exchange (ETDEWEB)

    Ahlstroem, Per-Eric (ed.) [Swedish Nuclear Fuel and Waste Management Co., Stockholm (Sweden); Andersson, Sofie; Ekberg, Christian; Liljenzin, Jan-Olov; Nilsson, Mikael; Skarnemark, Gunnar [Chalmers Univ. of Technology, Goeteborg (Sweden); Blomgren, Jan [Uppsala Univ. (Sweden). Dept. of Neutron Research; Eriksson, Marcus; Gudowski, Waclaw; Seltborg, Per; Wallenius, Jan; Sehgal, Bal Raj [Royal Inst. of Technology, Stockholm (Sweden)

    2004-05-01

    This report summarises the work reported in the years 1998-2003 and tries to assess the prospects for future development of partitioning and transmutation (P-T) as seen from a Swedish perspective. The R and D efforts on P-T have increased somewhat during the period 1998-2003. Research on P-T has taken a prominent role internationally in the R and D on future nuclear power and nuclear fuel cycle systems. Despite the fact that partitioning and transmutation have been on the agenda for quite a few years there are still a number of issues that must be settled before the research and development can be given a clearly focused direction. Studies propose research programmes for about six years at the cost of a couple of hundred million Euros. The construction of a small ADS experimental plant is a necessary step to develop and demonstrate the concept. This experimental plant should then be followed by a demonstration plant in almost full scale. Such a plant can at the earliest be ready in the mid-2030s. A number of circumstances have, however, contributed to slower speed, less intensity and lower funding than proposed in the studies. There is no unanimous view on the objectives for partitioning and transmutation. Many see it as a way to achieve broad acceptance for nuclear power at large. Others promote it as a way to get out of the impasse for a deep repository in several countries. Others again put a strong emphasise on the proliferation aspects. There is no unanimous view on the need to develop ADS or for the role of ADS in a P-T-system. Some advocate that ADS should be used for burning of all transuranium nuclides from the present enriched uranium fuelled light water reactors. Others see the ADS as a supplement particularly suitable for burning minor actinides (americium, curium and neptunium), whereas the major part of the plutonium should be burned in light water reactors (or in fast reactors) There is no consensus among experts on which technical route to follow

  7. Actinide Solubility and Speciation in the WIPP

    Energy Technology Data Exchange (ETDEWEB)

    Reed, Donald T. [Los Alamos National Laboratory

    2015-11-02

    The presentation begins with the role and need for nuclear repositories (overall concept, international updates (Sweden, Finland, France, China), US approach and current status), then moves on to the WIPP TRU repository concept (design, current status--safety incidents of February 5 and 14, 2014, path forward), and finally considers the WIPP safety case: dissolved actinide concentrations (overall approach, oxidation state distribution and redox control, solubility of actinides, colloidal contribution and microbial effects). The following conclusions are set forth: (1) International programs are moving forward, but at a very slow and somewhat sporadic pace. (2) In the United States, the Salt repository concept, from the perspective of the long-term safety case, remains a viable option for nuclear waste management despite the current operational issues/concerns. (3) Current model/PA prediction (WIPP example) are built on redundant conservatisms. These conservatisms are being addressed in the ongoing and future research to fill existing data gaps--redox control of plutonium by Fe(0, II), thorium (analog) solubility studies in simulated brine, contribution of intrinsic and biocolloids to the mobile concentration, and clarification of microbial ecology and effects.

  8. Evaluation of actinide biosorption by microorganisms

    Energy Technology Data Exchange (ETDEWEB)

    Happel, A.M.

    1996-06-01

    Conventional methods for removing metals from aqueous solutions include chemical precipitation, chemical oxidation or reduction, ion exchange, reverse osmosis, electrochemical treatment and evaporation. The removal of radionuclides from aqueous waste streams has largely relied on ion exchange methods which can be prohibitively costly given increasingly stringent regulatory effluent limits. The use of microbial cells as biosorbants for heavy metals offers a potential alternative to existing methods for decontamination or recovery of heavy metals from a variety of industrial waste streams and contaminated ground waters. The toxicity and the extreme and variable conditions present in many radionuclide containing waste streams may preclude the use of living microorganisms and favor the use of non-living biomass for the removal of actinides from these waste streams. In the work presented here, we have examined the biosorption of uranium by non-living, non-metabolizing microbial biomass thus avoiding the problems associated with living systems. We are investigating biosorption with the long term goal of developing microbial technologies for the remediation of actinides.

  9. End point control of an actinide precipitation reactor

    Energy Technology Data Exchange (ETDEWEB)

    Muske, K.R. [Villanova Univ., PA (United States). Dept. of Chemical Engineering; Palmer, M.J. [Los Alamos National Lab., NM (United States)

    1997-10-01

    The actinide precipitation reactors in the nuclear materials processing facility at Los Alamos National Laboratory are used to remove actinides and other heavy metals from the effluent streams generated during the purification of plutonium. These effluent streams consist of hydrochloric acid solutions, ranging from one to five molar in concentration, in which actinides and other metals are dissolved. The actinides present are plutonium and americium. Typical actinide loadings range from one to five grams per liter. The most prevalent heavy metals are iron, chromium, and nickel that are due to stainless steel. Removal of these metals from solution is accomplished by hydroxide precipitation during the neutralization of the effluent. An end point control algorithm for the semi-batch actinide precipitation reactors at Los Alamos National Laboratory is described. The algorithm is based on an equilibrium solubility model of the chemical species in solution. This model is used to predict the amount of base hydroxide necessary to reach the end point of the actinide precipitation reaction. The model parameters are updated by on-line pH measurements.

  10. Separation of actinides from spent nuclear fuel: A review.

    Science.gov (United States)

    Veliscek-Carolan, Jessica

    2016-11-15

    This review summarises the methods currently available to extract radioactive actinide elements from solutions of spent nuclear fuel. This separation of actinides reduces the hazards associated with spent nuclear fuel, such as its radiotoxicity, volume and the amount of time required for its' radioactivity to return to naturally occurring levels. Separation of actinides from environmental water systems is also briefly discussed. The actinide elements typically found in spent nuclear fuel include uranium, plutonium and the minor actinides (americium, neptunium and curium). Separation methods for uranium and plutonium are reasonably well established. On the other hand separation of the minor actinides from lanthanide fission products also present in spent nuclear fuel is an ongoing challenge and an area of active research. Several separation methods for selective removal of these actinides from spent nuclear fuel will be described. These separation methods include solvent extraction, which is the most commonly used method for radiochemical separations, as well as the less developed but promising use of adsorption and ion-exchange materials.

  11. Thin extractive membrane for monitoring actinides in aqueous streams.

    Science.gov (United States)

    Chavan, Vivek; Paul, Sumana; Pandey, Ashok K; Kalsi, P C; Goswami, A

    2013-09-15

    Alpha spectrometry and solid state nuclear track detectors (SSNTDs) are used for monitoring ultra-trace amount of alpha emitting actinides in different aqueous streams. However, these techniques have limitations i.e. alpha spectrometry requires a preconcentration step and SSNTDs are not chemically selective. Therefore, a thin polymer inclusion membrane (PIM) supported on silanized glass was developed for preconcentraion and determination of ultra-trace concentration of actinides by α-spectrometry and SSNTDs. PIMs were formed by spin coating on hydrophobic glass slide or solvent casting to form thin and self-supported membranes, respectively. Sorption experiments indicated that uptakes of actinides in the PIM were highly dependent on acidity of solution i.e. Am(III) sorbed up to 0.1 molL(-1) HNO₃, U(VI) up to 0.5 molL(-1) HNO₃ and Pu(IV) from HNO₃ concentration as high as 4 molL(-1). A scheme was developed for selective sorption of target actinide in the PIM by adjusting acidity and oxidation state of actinide. The actinides sorbed in PIMs were quantified by alpha spectrometry and SSNTDs. For SSNTDs, neutron induced fission-fragment tracks and α-particle tracks were registered in Garware polyester and CR-39 for quantifications of natural uranium and α-emitting actinides ((241)Am/(239)Pu/(233)U), respectively. Finally, the membranes were tested to quantify Pu in 4 molL(-1) HNO3 solutions and synthetic urine samples.

  12. Crystal growth methods dedicated to low solubility actinide oxalates

    Energy Technology Data Exchange (ETDEWEB)

    Tamain, C., E-mail: christelle.tamain@cea.fr [CEA, Nuclear Energy Division, Marcoule, RadioChemistry & Processes Department, F-30207 Bagnols sur Cèze (France); Arab-Chapelet, B. [CEA, Nuclear Energy Division, Marcoule, RadioChemistry & Processes Department, F-30207 Bagnols sur Cèze (France); Rivenet, M. [University Lille Nord de France, Unité de Catalyse et de Chimie du Solide, UCCS UMR CNRS 8181, ENSCL-USTL, B.P. 90108, F-59652 Villeneuve d’Ascq Cedex (France); Grandjean, S. [CEA, Nuclear Energy Division, Marcoule, RadioChemistry & Processes Department, F-30207 Bagnols sur Cèze (France); Abraham, F. [University Lille Nord de France, Unité de Catalyse et de Chimie du Solide, UCCS UMR CNRS 8181, ENSCL-USTL, B.P. 90108, F-59652 Villeneuve d’Ascq Cedex (France)

    2016-04-15

    Two novel crystal growth syntheses dedicated to low solubility actinide-oxalate systems and adapted to glove box handling are described. These methods based on the use of precursors of either actinide metal or oxalic acid have been optimized on lanthanide systems (analogue of actinides(III)) and then assessed on real actinide systems. They allow the synthesis of several actinide oxalate single crystals, Am{sub 2}(C{sub 2}O{sub 4}){sub 3}(H{sub 2}O){sub 3}·xH{sub 2}O, Th(C{sub 2}O{sub 4}){sub 2}·6H{sub 2}O, M{sub 2+x}[Pu{sup IV}{sub 2−x}Pu{sup III}{sub x}(C{sub 2}O{sub 4}){sub 5}]·nH{sub 2}O and M{sub 1−x}[Pu{sup III}{sub 1−x}Pu{sup IV}{sub x}(C{sub 2}O{sub 4}){sub 2}·H{sub 2}O]·nH{sub 2}O. It is the first time that these well-known compounds are formed by crystal growth methods, thus enabling direct structural studies on transuranic element systems and acquisition of basic data beyond deductions from isomorphic (or not) lanthanide compounds. Characterizations by X-ray diffraction, UV–visible solid spectroscopy, demonstrate the potentialities of these two crystal growth methods to obtain oxalate compounds. - Graphical abstract: Two new single crystal growth methods dedicated to actinide oxalate compounds. - Highlights: • Use of diester as oxalate precursor for crystal growth of actinide oxalates. • Use of actinide oxide as precursor for crystal growth of actinide oxalates. • Crystal growth of Pu(III) and Am(III) oxalates. • Crystal growth of mixed Pu(III)/Pu(IV) oxalates.

  13. Capability ethics

    NARCIS (Netherlands)

    I.A.M. Robeyns (Ingrid)

    2012-01-01

    textabstractThe capability approach is one of the most recent additions to the landscape of normative theories in ethics and political philosophy. Yet in its present stage of development, the capability approach is not a full-blown normative theory, in contrast to utilitarianism, deontological

  14. Capability ethics

    NARCIS (Netherlands)

    I.A.M. Robeyns (Ingrid)

    2012-01-01

    textabstractThe capability approach is one of the most recent additions to the landscape of normative theories in ethics and political philosophy. Yet in its present stage of development, the capability approach is not a full-blown normative theory, in contrast to utilitarianism, deontological theor

  15. Capability ethics

    NARCIS (Netherlands)

    I.A.M. Robeyns (Ingrid)

    2012-01-01

    textabstractThe capability approach is one of the most recent additions to the landscape of normative theories in ethics and political philosophy. Yet in its present stage of development, the capability approach is not a full-blown normative theory, in contrast to utilitarianism, deontological theor

  16. ORNL actinide materials and a new detection system for superheavy nuclei

    Directory of Open Access Journals (Sweden)

    Rykaczewski Krzysztof P.

    2016-01-01

    Full Text Available The actinide resources and production capabilities at Oak Ridge National Laboratory (ORNL are reviewed, including potential electromagnetic separation of rare radioactive materials. The first experiments at the Dubna Gas Filled Recoil Separator (DGFRS with a new digital detection system developed at ORNL and University of Tennessee Knoxville (UTK are presented. These studies used 240Pu material provided by ORNL and mixed-Cf targets made at ORNL. The proposal to use an enriched 251Cf target and a large dose of 58Fe beam to reach the N = 184 shell closure and to observe new elements with Z = 124, 122 and 120 is discussed.

  17. Optimizing SFR transmutation performance through direct adjoining control theory

    Science.gov (United States)

    Davis, Jeffrey C.

    2007-12-01

    We have developed the CORTANA code to optimize the transmutation performance of sodium cooled fast reactors (SFRs). We obtain the necessary conditions for optimal fuel and burnable absorber loadings using Pontryagin's maximum principle with a direct adjoining approach to explicitly account for either a flat flux or a power peaking inequality constraint providing a set of coupled system, Euler-Lagrange (E-L), and optimality equations which are iteratively solved with the method of conjugate gradients until no further improvement in the objective function is achieved. To satisfy the inequality constraints throughout the operating cycle, we have implemented a backwards diffusion theory (BDT) to establish a relationship between fuel loading and the relative assembly power distribution during the cycle and systematically eliminate the constraint violations with each conjugate gradient iteration. The CORTANA SFR optimization code uses multi-group, three-dimensional neutron diffusion theory, with a microscopic depletion scheme. We solve the system equations in a quasi-static fashion forward in time from beginning-of-cycle (BOC) to end-of-cycle (EOC), while we solve the E-L equations backwards in time from EOC to BOC, reflecting the adjoint nature of the Lagrange multipliers. A two enrichment-zone SFR problem verifies our formulation, yielding a TRU enrichment distribution nearly identical to that of the reference SFR core in the Generation IV Roadmap. Using a full heavy metal recycling mode, we coupled our optimization methodology with the REBUS-3 equilibrium cycle methodology to optimize an SFR operating as a second tier transmuter. We model the system using a three-dimensional triangular-z finite differencing scheme with full core symmetry and a time-independent 33-group microscopic cross section library. Beginning from a uniform TRU distribution, our CORTANA improves the SFR performance by reducing the maximum relative assembly power from 1.7 to 1.25, minimizes

  18. Transmutation of Isotopes --- Ecological and Energy Production Aspects

    Science.gov (United States)

    Gudowski, Waclaw

    2000-01-01

    This paper describes principles of Accelerator-Driven Transmutation of Nuclear Wastes (ATW) and gives some flavour of the most important topics which are today under investigations in many countries. An assessment of the potential impact of ATW on a future of nuclear energy is also given. Nuclear reactors based on self-sustained fission reactions --- after spectacular development in fifties and sixties, that resulted in deployment of over 400 power reactors --- are wrestling today more with public acceptance than with irresolvable technological problems. In a whole spectrum of reasons which resulted in today's opposition against nuclear power few of them are very relevant for the nuclear physics community and they arose from the fact that development of nuclear power had been handed over to the nuclear engineers and technicians with some generically unresolved problems, which should have been solved properly by nuclear scientists. In a certain degree of simplification one can say, that most of the problems originate from very specific features of a fission phenomenon: self-sustained chain reaction in fissile materials and very strong radioactivity of fission products and very long half-life of some of the fission and activation products. And just this enormous concentration of radioactive fission products in the reactor core is the main problem of managing nuclear reactors: it requires unconditional guarantee for the reactor core integrity in order to avoid radioactive contamination of the environment; it creates problems to handle decay heat in the reactor core and finally it makes handling and/or disposal of spent fuel almost a philosophical issue, due to unimaginable long time scales of radioactive decay of some isotopes. A lot can be done to improve the design of conventional nuclear reactors (like Light Water Reactors); new, better reactors can be designed but it seems today very improbable to expect any radical change in the public perception of conventional

  19. Distribution of actinides in SFR1; Aktinidfoerdelning i SFR1

    Energy Technology Data Exchange (ETDEWEB)

    Ingemansson, Tor [ALARA Engineering, Skultuna (Sweden)

    2000-02-01

    The amount of actinides in the Swedish repository for intermediate level radioactive wastes has been estimated. The sources for the actinides are mainly the purification filters of the reactors and the used fuel pools. Defect fuel elements are the originating source of the actinides. It is estimated that the 12 Swedish reactors, in total, have had 2.2 kg of fuel dissolved in their systems since start-up. About 880 g of this amount has been brought to the intermediate-level repository.

  20. Self-interaction corrected local spin density calculations of actinides

    DEFF Research Database (Denmark)

    Petit, Leon; Svane, Axel; Szotek, Z

    2010-01-01

    We use the self-interaction corrected local spin-density approximation in order to describe localization-delocalization phenomena in the strongly correlated actinide materials. Based on total energy considerations, the methodology enables us to predict the ground-state valency configuration...... of the actinide ions in these compounds from first principles. Here we review a number of applications, ranging from electronic structure calculations of actinide metals, nitrides and carbides to the behaviour under pressure of intermetallics, and O vacancies in PuO2....

  1. Separating the Minor Actinides Through Advances in Selective Coordination Chemistry

    Energy Technology Data Exchange (ETDEWEB)

    Lumetta, Gregg J.; Braley, Jenifer C.; Sinkov, Sergey I.; Carter, Jennifer C.

    2012-08-22

    This report describes work conducted at the Pacific Northwest National Laboratory (PNNL) in Fiscal Year (FY) 2012 under the auspices of the Sigma Team for Minor Actinide Separation, funded by the U.S. Department of Energy Office of Nuclear Energy. Researchers at PNNL and Argonne National Laboratory (ANL) are investigating a simplified solvent extraction system for providing a single-step process to separate the minor actinide elements from acidic high-level liquid waste (HLW), including separating the minor actinides from the lanthanide fission products.

  2. Electronic structure and ionicity of actinide oxides from first principles

    DEFF Research Database (Denmark)

    Petit, Leon; Svane, Axel; Szotek, Z.

    2010-01-01

    The ground-state electronic structures of the actinide oxides AO, A2O3, and AO2 (A=U, Np, Pu, Am, Cm, Bk, and Cf) are determined from first-principles calculations, using the self-interaction corrected local spin-density approximation. Emphasis is put on the degree of f-electron localization, which...... in the actinide dioxides is discussed, and it is found that the dioxide is the most stable oxide for the actinides from Np onward. Our study reveals a strong link between preferred oxidation number and degree of localization which is confirmed by comparing to the ground-state configurations of the corresponding...

  3. An emergency bioassay method for actinides in urine.

    Science.gov (United States)

    Dai, Xiongxin; Kramer-Tremblay, Sheila

    2011-08-01

    A rapid bioassay method has been developed for the sequential measurements of actinides in human urine samples. The method involves actinide separation from a urine matrix by co-precipitation with hydrous titanium oxide (HTiO), followed by anion exchange and extraction chromatography column purification, and final counting by alpha spectrometry after cerium fluoride micro-precipitation. The minimal detectable activities for the method were determined to be 20 mBq L(-1) or less for plutonium, uranium, americium and curium isotopes, with an 8-h sample turn-around time. Spike tests showed that this method would meet the requirements for actinide bioassay following a radiation emergency.

  4. Fabrication of uranium-based ceramics using internal gelation for the conversion of trivalent actinides; Herstellung uranbasierter Keramiken mittel interner Gelierung zur Konversion trivalenter Actinoiden

    Energy Technology Data Exchange (ETDEWEB)

    Daniels, Henrik

    2012-07-01

    Alternative to today's direct final waste disposal strategy of long-lived radionuclides, for example the minor actinides neptunium, americium, curium and californium, is their selective separation from the radioactive wastestream with subsequent transmutation by neutron irradiation. Hereby it is possible to obtain nuclides with a lower risk-potential concerning their radiotoxicity. 1 neutron irradiation can be carried out either with neutron sources or in the next generation of nuclear reactors. Before the treatment, the minor actinides need to be converted in a suitable chemical and physical form. Internal gelation offers a route through which amorphous gel-spheres can be obtained directly from a metal-salt solution. Due to the presence of different types of metal ions as well as changing pH-values in a stock solution, a complex hydrolysis behaviour of these elements before and during gelation occurs. Therefore, investigations with uranium and neodymium as a minor actinide surrogate were carried out. As a result of suitable gelation-parameters, uraniumneodymium gel-spheres were successfully synthesised. The spheres also stayed intact during the subsequent thermal treatment. Based upon these findings, uranium-plutonium and uranium-americium gels were successfully created. For theses systems, the determined parameters for the uraniumneodymium gelation could also be applied. Additionally, investigations to reduce the acidity of uranium-based stock solutions for internal gelation were carried out. The necessary amount of urea and hexamethylenetetramine to induce gelation could hereby be decreased. This lead to a general increase of the gel quality and made it possible to carry out uranium-americium gelation in the first place. To investigate the stability of urea and hexamethylenetetramine, solutions of these chemicals were irradiated with different radiation doses. These chemicals showed a high stability against radiolysis in aqueous solutions.

  5. HYPERFUSE: a hypervelocity inertial confinement system for fusion energy production and fission waste transmutation

    Energy Technology Data Exchange (ETDEWEB)

    Makowitz, H.; Powell, J.R.; Wiswall, R.

    1980-01-01

    Parametric system studies of an inertial confinement fusion (ICF) reactor system to transmute fission products from a LWR economy have been carried out. The ICF reactors would produce net power in addition to transmuting fission products. The particular ICF concept examined is an impact fusion approach termed HYPERFUSE, in which hypervelocity pellets, traveling on the order of 100 to 300 km/sec, collide with each other or a target block in a reactor chamber and initiate a thermonuclear reaction. The DT fusion fuel is contained in a shell of the material to be transmuted, e.g., /sup 137/Cs, /sup 90/Sr, /sup 129/I, /sup 99/Tc, etc. The 14-MeV fusion neutrons released during the pellet burn cause transmutation reactions (e.g., (n,2n), (n,..cap alpha..), (n,..gamma..), etc.) that convert the long-lived fission products (FP's) either to stable products or to species that decay with a short half-life to a stable product. The transmutation parametric studies conclude that the design of the hypervelocity projectiles should emphasize the achievement of high densities in the transmutation regions (greater than the DT fusion fuel density), as well as the DT ignition and burn criterion (rho R = 1.0 to 3.0) requirements. These studies also indicate that masses on the order of 1.0 g at densities of rho greater than or equal to 500.0 g/cm/sup 3/ are required for a practical fusion-based fission product transmutation system.

  6. {sup 129}I targets for studies of nuclear waste transmutation

    Energy Technology Data Exchange (ETDEWEB)

    Ingelbrecht, C. E-mail: ingelbrecht@irmm.jrc.be; Lupo, J.; Raptis, K.; Altzitzoglou, T.; Noguere, G

    2002-03-11

    Nuclear incineration of long-lived fission products and minor actinides is being investigated as an alternative means of reactor waste disposal. {sup 129}I is of particular interest because of its long half-life and high mobility in the environment. Lead iodide targets of {sup 129}I for neutron capture cross-section measurements were prepared from 210 l fuel reprocessing waste solution containing 1.3 g l{sup -1} iodine and other fission products. The iodine was separated by oxidation to I{sub 2} and extraction into chloroform, reduction to iodide by sodium sulphite and re-extraction into an aqueous phase. Iodide was precipitated using lead nitrate and dried. The chemistry was carried out batch-wise using 400 ml starting solution each time and recycling the chloroform. An extraction efficiency of about 90%, determined by {gamma}-ray spectrometry, was achieved.

  7. Physics Characterization of a Heterogeneous Sodium Fast Reactor Transmutation System

    Energy Technology Data Exchange (ETDEWEB)

    Samuel E. Bays

    2007-09-01

    The threshold-fission (fertile) nature of Am-241 is used to destroy this minor actinide by capitalizing upon neutron capture instead of fission within a sodium fast reactor. This neutron-capture and its subsequent decay chain leads to the breeding of even mass number plutonium isotopes. A slightly moderated target design is proposed for breeding plutonium in an axial blanket located above the active “fast reactor” driver fuel region. A parametric study on the core height and fuel pin diameter-to-pitch ratio is used to explore the reactor and fuel cycle aspects of this design. This study resulted in both a non-flattened and a pancake core geometry. Both of these designs demonstrated a high capacity for removing americium from the fuel cycle. A reactivity coefficient analysis revealed that this heterogeneous design will have comparable safety aspects to a homogeneous reactor of the same size.

  8. Transmutation of nuclear waste in accelerator-driven systems

    CERN Document Server

    Herrera-Martínez, A

    2004-01-01

    Today more than ever energy is not only a cornerstone of human development, but also a key to the environmental sustainability of economic activity. In this context, the role of nuclear power may be emphasized in the years to come. Nevertheless, the problems of nuclear waste, safety and proliferation still remain to be solved. It is believed that the use of accelerator-driven systems (ADSs) for nuclear waste transmutation and energy production would address these problems in a simple, clean and economically viable, and therefore sustainable, manner. This thesis covers the major nuclear physics aspects of ADSs, in particular the spallation process and the core neutronics specific to this type of systems. The need for accurate nuclear data is described, together with a detailed analysis of the specific isotopes and energy ranges in which this data needs to be improved and the impact of their uncertainty. Preliminary experimental results for some of these isotopes, produced by the Neutron Time-of-Flight (n_TOF) ...

  9. Dark energy and dimensional transmutation in $R^2$ gravity

    CERN Document Server

    Maggiore, Michele

    2015-01-01

    Recent work has shown that non-local modifications of gravity involving terms such as $m^2R\\Box^{-2}R$ (and no cosmological constant) provide a phenomenologically viable alternative to $\\Lambda$CDM. We discuss the possibility that such non-local terms emerge in the far infrared from the running of the coupling constant associated to the $R^2$ term in higher-derivative gravity, which is asymptotically free in the ultraviolet and strongly coupled in the infrared. In this scenario the mass scale $m$ of the non-local model emerges from dimensional transmutation, similarly to $\\Lambda_{\\rm QCD}$ for strong interactions, leading to a technically natural value of the scale associated to dark energy. We also argue that the emergence of the non-local term can be understood as a dynamical mass generation for the conformal mode, as a response of the vacuum to the strong infrared fluctuations that are generated by the anomaly-induced effective action.

  10. Naturalness and Dimensional Transmutation in Classically Scale-Invariant Gravity

    CERN Document Server

    Einhorn, Martin B

    2014-01-01

    We discuss the nature of quantum field theories involving gravity that are classically scale-invariant. We show that gravitational radiative corrections are crucial in the determination of the nature of the vacuum state in such theories, which are renormalisable, technically natural, and can be asymptotically free in all dimensionless couplings. In the pure gravity case, we discuss the role of the Gauss-Bonnet term, and we find that Dimensional Transmutation (DT) \\`a la Coleman-Weinberg leads to extrema of the effective action corresponding to nonzero values of the curvature, but such that these extrema are local maxima. In even the simplest extension of the theory to include scalar fields, we show that the same phenomenon can lead to extrema that are local minima of the effective action, with both non-zero curvature and non-zero scalar vacuum expectation values, leading to spontaneous generation of the Planck mass. Although we find an asymptotically free (AF) fixed point exists, unfortunately, no running of ...

  11. Transmutation of nuclear waste in accelerator-driven systems

    CERN Document Server

    Herrera-Martínez, A

    2004-01-01

    Today more than ever energy is not only a cornerstone of human development, but also a key to the environmental sustainability of economic activity. In this context, the role of nuclear power may be emphasized in the years to come. Nevertheless, the problems of nuclear waste, safety and proliferation still remain to be solved. It is believed that the use of accelerator-driven systems (ADSs) for nuclear waste transmutation and energy production would address these problems in a simple, clean and economically viable, and therefore sustainable, manner. This thesis covers the major nuclear physics aspects of ADSs, in particular the spallation process and the core neutronics specific to this type of systems. The need for accurate nuclear data is described, together with a detailed analysis of the specific isotopes and energy ranges in which this data needs to be improved and the impact of their uncertainty. Preliminary experimental results for some of these isotopes, produced by the Neutron Time-of-Flight (n_TOF) ...

  12. Second International Conference on Neutron Transmutation Doping in Semiconductors

    CERN Document Server

    Neutron Transmutation Doping in Semiconductors

    1979-01-01

    This volume contains the invited and contributed papers presented at the Second International Conference on Neutron Transmutation Doping in Semiconductors held April 23-26, 1978 at the University of Missouri-Columbia. The first "testing of the waters" symposium on this subject was organized by John Cleland and Dick Wood of the Solid-State Division of Oak Ridge National Laboratory in April of 1976, just one year after NTD-silicon appeared on the marketplace. Since this first meeting, NTD-silicon has become established as the starting material for the power device industry and reactor irradiations are now measured in tens of tons of material per annum making NTD processing the largest radiation effects technology in the semiconductor industry. Since the first conference at Oak Ridge, new applications and irradiation techniques have developed. Interest in a second con­ ference and in publishing the proceedings has been extremely high. The second conference at the University of Missouri was attended by 114 perso...

  13. Study of radioactive impurities in neutron transmutation doped germanium

    Energy Technology Data Exchange (ETDEWEB)

    Mathimalar, S.; Dokania, N.; Singh, V. [India-based Neutrino Observatory, Tata Institute of Fundamental Research, Mumbai 400 005 (India); Homi Bhabha National Institute, Anushaktinagar, Mumbai 400 094 (India); Nanal, V., E-mail: nanal@tifr.res.in [Department of Nuclear and Atomic Physics, Tata Institute of Fundamental Research, Mumbai 400 005 (India); Pillay, R.G. [Department of Nuclear and Atomic Physics, Tata Institute of Fundamental Research, Mumbai 400 005 (India); Shrivastava, A. [Nuclear Physics Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India); Jagadeesan, K.C.; Thakare, S.V. [Isotope Production and Applications Division, Bhabha Atomic Research Centre, Mumbai 400 085 (India)

    2015-02-21

    A program to develop low temperature (mK) sensors with neutron transmutation doped Ge for rare event studies with a cryogenic bolometer has been initiated. For this purpose, semiconductor grade Ge wafers are irradiated with thermal neutron flux from Dhruva reactor at Bhabha Atomic Research Centre (BARC), Mumbai. Spectroscopic studies of irradiated samples have revealed that the environment of the capsule used for irradiating the sample leads to significant levels of {sup 65}Zn, {sup 110m}Ag and {sup 182}Ta impurities, which can be reduced by chemical etching of approximately ∼50μm thick surface layer. From measurements of the etched samples in the low background counting setup, activity due to trace impurities of {sup 123}Sb in bulk Ge is estimated to be ∼1Bq/g after irradiation. These estimates indicate that in order to use the NTD Ge sensors for rare event studies, a cooldown period of ∼2 years would be necessary to reduce the radioactive background to ≤1mBq/g.

  14. Compton Radiation for Nuclear Waste Management and Transmutation

    Science.gov (United States)

    Bulyak, E.; Urakawa, J.

    2015-10-01

    Compton inverse radiation is emitted in the process of backscattering of the laser pulses off the relativistic electrons. This radiation possesses high spectral density and high energy of photons--in hard x-ray up to gammaray energy range--with moderate electron energies (hundreds of MeV up to 1 GeV) due to short wavelength of the laser radiation. The Compton radiation is well collimated: emitting within a narrow cone along the electron beam. A distinct property of the Compton inverse radiation is a steep high-energy cutoff of the spectrum and the maximal intensity just below the cutoff. The Compton sources can attain: spectral density up to 1014 gammas/(s 0.1%bandwidth) in MeV range of energies, and spectral brightness up to 1020 gammas/(smm2mr2 0.1% bw). Applicability of Compton sources for nuclear waste management and detection of radioisotopes and fissionable nuclides are discussed in the report. Also application limits of Compton gamma sources for transmutation of radioactive isotopes are estimated. A recently proposed subtracting method, in which two sets of data obtained by irradiating the object by the Compton beams with slightly different maximal energies are compared, will enhance resolution of detection radioactive elements at the 'atomic' (hundreds of keV) and the 'nuclear' (a few MeV) photon energies.

  15. Factors affecting the placental transfer of actinides

    Energy Technology Data Exchange (ETDEWEB)

    Sikov, M.R.; Kelman, B.J. (Pacific Northwest Laboratory, Richland, WA (USA))

    1989-01-01

    The primary goal of this paper is to consider factors that affect the availability and transport of actinides from maternal blood, through the placenta, to the conceptus. These factors, of particular importance in scaling results from animals to man, include the route and temporal pattern of administration, the mass and physicochemical state of material administered, metabolism of the pregnant animal and fetal organs or tissue, and species-specific changes in placental structure relative to stage of gestation at exposure. Preliminary concepts for descriptive and kinetic models are proposed to integrate these results, to identify additional information required for developing more comprehensive models, and to provide a basis for scaling to human pregnancies for purposes of radiation dosimetry.

  16. Solidification of simulated actinides by natural zircon

    Institute of Scientific and Technical Information of China (English)

    YANG Jian-Wen; LUO Shang-Geng

    2004-01-01

    Natural zircon was used as precursor material to produce a zircon waste form bearing 20wt% simulated actinides (Nd2O3 and UO2) through a solid state reaction by a typical synroc fabrication process. The fabricated zircon waste form has relatively good physical properties (density 5.09g/cm3, open porosity 4.0%, Vickers hardness 715kg/mm2). The XRD, SEM/EDS and TEM/EDS analyses indicate that there are zircon phases containing waste elements formed through the reaction. The chemical durability and radiation stability are determined by the MCC-1method and heavy ion irradiation; the results show that the zircon waste form is highly leach resistance and relatively stable under irradiation (amorphous dose 0.7dpa). From this study, the method of using a natural mineral to solidify radioactive waste has proven to be feasible.

  17. Gamma spectroscopy of neutron rich actinide nuclei

    Energy Technology Data Exchange (ETDEWEB)

    Birkenbach, Benedikt; Geibel, Kerstin; Vogt, Andreas; Hess, Herbert; Reiter, Peter; Steinbach, Tim; Schneiders, David [Koeln Univ. (Germany). IKP; Collaboration: AGATA-Collaboration

    2013-07-01

    Excited states in neutron-rich actinide Th and U nuclei were investigated after multi nucleon transfer reactions employing the AGATA demonstrator and PRISMA setup at LNL (INFN, Italy). A primary {sup 136}Xe beam of 1 GeV hitting a {sup 238}U target was used to produce the nuclei of interest. Beam-like reaction products of Xe- and Ba isotopes after neutron transfer were selected by the PRISMA spectrometer. The recoil like particles were registered by a MCP detector inside the scattering chamber. Coincident γ-rays from excited states in beam and target like particles were measured with the position sensitive AGATA HPGe detectors. Improved Doppler correction and quality of the γ-spectra is based on the novel γ-ray tracking technique which was successfully exploited. First results on the collective properties of various Th and U isotopes are discussed.

  18. Dynamic capabilities

    DEFF Research Database (Denmark)

    Grünbaum, Niels Nolsøe; Stenger, Marianne

    2013-01-01

    it was dominated by a lack of systematism, assessment, monitoring, marketing speculations and feasibility calculation. Furthermore, the sphere was dictated by asymmetric supplier-customer relationships and negotiation power leading, among other possible factors, to meager profitability.......The consequences of dynamic capabilities (i.e. innovation performance and profitability) is an under researched area in the growing body of literature on dynamic capabilities and innovation management. This study aims to examine the relationship between dynamic capabilities, innovation performance...... and profitability of small and medium sized manufacturing enterprises operating in volatile environments. A multi-case study design was adopted as research strategy. The findings reveal a positive relationship between dynamic capabilities and innovation performance in the case companies, as we would expect. It was...

  19. Radiochemical studies of neutron deficient actinide isotopes

    Energy Technology Data Exchange (ETDEWEB)

    Williams, K.E.

    1978-04-01

    The production of neutron deficient actinide isotopes in heavy ion reactions was studied using alpha, gamma, x-ray, and spontaneous fission detection systems. A new isotope of berkelium, /sup 242/Bk, was produced with a cross-section of approximately 10 ..mu..b in reactions of boron on uranium and nitrogen on thorium. It decays by electron capture with a half-life of 7.0 +- 1.3 minutes. The alpha-branching ratio for this isotope is less than 1% and the spontaneous fission ratio is less than 0.03%. Studies of (Heavy Ion, pxn) and (Heavy Ion, ..cap alpha..xn) transfer reactions in comparison with (Heavy ion, xn) compound nucleus reactions revealed transfer reaction cross-sections equal to or greater than the compound nucleus yields. The data show that in some cases the yield of an isotope produced via a (H.I.,pxn) or (H.I.,..cap alpha..xn) reaction may be higher than its production via an xn compound nucleus reaction. These results have dire consequences for proponents of the ''Z/sub 1/ + Z/sub 2/ = Z/sub 1+2/'' philosophy. It is no longer acceptable to assume that (H.I.,pxn) and (H.I.,..cap alpha..xn) product yields are of no consequence when studying compound nucleus reactions. No evidence for spontaneous fission decay of /sup 228/Pu, /sup 230/Pu, /sup 232/Cm, or /sup 238/Cf was observed indicating that strictly empirical extrapolations of spontaneous fission half-life data is inadequate for predictions of half-lives for unknown neutron deficient actinide isotopes.

  20. Studies of actinides in a superanoxic fjord

    Energy Technology Data Exchange (ETDEWEB)

    Roos, P.

    1997-04-01

    Water column and sediment profiles of Pu, Am, Th and U have been obtained in the superanoxic Framvaren fjord, southern Norway. The concentration of bomb test fallout Pu, Am as well as `dissolved` Th in the bottom water are the highest recorded in the marine environment. The behaviour of the actinides in the anoxic water mass is to a large extent governed by the behaviour of the colloidal material. Ultrafiltration reveals that 40-60% of the actinides are associated to the large colloids, surprisingly this is valid also for U. The sediment acts as a source for Pu, Am, and Th to the water column but primarily as a sink for U. The remobilization of Pu, Am and Th is evident from the water column profiles which have similar diffusion shape profiles as other constituents originating from the sediments. The vertical eddy diffusion coefficient calculated from the Pu profile is in the same order of magnitude as reported from the H{sub 2}S profile. Decreased bottom water concentrations (but a constant water column inventory) between 1989 and 1995 as well as pore water Pu concentrations nearly identical to the overlaying bottom water indicates that the present Pu flux from the sediments are low. Contrary to Pu and Am, the water column Th inventory ({sup 232}Th and {sup 230}Th) continues to increase. The flux of {sup 232}Th from the sediments was determined from changes in water column inventory between 1989 and 1995 and from a pore water profile to be in the order of 2-8 Bq/m{sup 2}/y. 208 refs.

  1. Pyrometallurgical processes for recovery of actinide elements

    Energy Technology Data Exchange (ETDEWEB)

    Battles, J.E.; Laidler, J.J.; McPheeters, C.C.; Miller, W.E.

    1994-01-01

    A metallic fuel alloy, nominally U-20-Pu-lOZr, is the key element of the Integral Fast Reactor (IFR) fuel cycle. Metallic fuel permits the use of an innovative, simple pyrometallurgical process, known as pyroprocessing, (the subject of this report), which features fused salt electrorefining of the spent fuel. Electrorefining separates the actinide elements from fission products, without producing a separate stream of plutonium. The plutonium-bearing product is contaminated with higher actinides and with a minor amount of rare earth fission products, making it diversion resistant while still suitable as a fuel material in the fast spectrum of the IFR core. The engineering-scale demonstration of this process will be conducted in the refurbished EBR-II Fuel Cycle Facility, which has entered the start-up phase. An additional pyrometallurgical process is under development for extracting transuranic (TRU) elements from Light Water Reactor (LWR) spent fuel in a form suitable for use as a feed to the IFR fuel cycle. Four candidate extraction processes have been investigated and shown to be chemically feasible. The main steps in each process are oxide reduction with calcium or lithium, regeneration of the reductant and recycle of the salt, and separation of the TRU product from the bulk uranium. Two processes, referred to as the lithium and salt transport (calcium reductant) processes, have been selected for engineering-scale demonstration, which is expected to start in late 1993. An integral part of pyroprocessing development is the treatment and packaging of high-level waste materials arising from the operations, along with the qualification of these waste forms for disposal in a geologic repository.

  2. Transmutation performance analysis on coolant options in a hybrid reactor system design for high level waste incineration

    Energy Technology Data Exchange (ETDEWEB)

    Hong, Seong-Hee; Siddique, Muhammad Tariq; Kim, Myung Hyun, E-mail: mhkim@khu.ac.kr

    2015-11-15

    Highlights: • Waste transmutation performance was compared and analyzed for seven different coolant options. • Reactions of fission and capture showed big differences depending on coolant options. • Moderation effect significantly affects on energy multiplication, tritium breeding and waste transmutation. • Reduction of radio-toxicities of TRUs showed different trend to coolant choice from performance of waste transmutation. - Abstract: A fusion–fission hybrid reactor (FFHR) is one of the most attractive candidates for high level waste transmutation. The selection of coolant affects the transmutation performance of a FFHR. LiPb coolant, as a conventional coolant for a FFHR, has problems such as reduction in neutron economic and magneto-hydro dynamics (MHD) pressure drop. Therefore, in this work, transmutation performance is evaluated and compared for various coolant options such as LiPb, H{sub 2}O, D{sub 2}O, Na, PbBi, LiF-BeF{sub 2} and NaF-BeF{sub 2} applicable to a hybrid reactor for waste transmutation (Hyb-WT). Design parameters measuring performance of a hybrid reactor were evaluated by MCNPX. They are k{sub eff}, energy multiplication factor, neutron absorption ratio, tritium breeding ratio, waste transmutation ratio, support ratio and radiotoxicity reduction. Compared to LiPb, H{sub 2}O and D{sub 2}O are not suitable for waste transmutation because of neutron moderation effect. Waste transmutation performances with Na and PbBi are similar to each other and not different much from LiPb. Even though molten salt such as LiF-BeF{sub 2} and NaF-BeF{sub 2} is good for avoiding MHD pressure drop problem, waste transmutation performance is dropped compared with LiPb.

  3. Element Partitioning in Glass-Ceramic Designed for Actinides Immobilization

    Institute of Scientific and Technical Information of China (English)

    2008-01-01

    <正>Glass-ceramics were designed for immobilization of actinides. In order to immobilizing more wastes in the matrix and to develop the optimum formulation for the glass-ceramic, it is necessary to study the

  4. Advanced techniques for actinide spectroscopy (ATAS 2012). Abstract book

    Energy Technology Data Exchange (ETDEWEB)

    Foerstendorf, Harald; Mueller, Katharina; Steudtner, Robin (eds.)

    2012-07-01

    The abstract book of the International workshop on advanced techniques for actinide spectroscopy (ATAS 2012) include contributions concerning the following issues: environmental applications, NMR spectroscopy, vibrational spectroscopy, X-ray spectroscopy and theory, technical application: separation processes, emission spectroscopy.

  5. Zirconium and technetium recovery and partitioning in the presence of actinides in modified Purex process for ATW program. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Dzekun, E.G.; Fedorov, Y.S.; Galkin, B.Y.; Lyubtsev, R.I.; Mashkin, A.N.; Mishin, E.N.; Zilberman, B.Y. [Radievyj Inst., Leningrad (Russian Federation)

    1994-12-31

    The modified Purex process flowsheet is based on combination of all irradiated materials, their joint dissolution and reprocessing as a NPP spent fuel solution with abnormal Pu content after addition of recycled depleted U concentrate. Some groups of long-lived radionuclides could be completely recovered and localized at the stage of extraction reprocessing using 30% TBP. Studies were conducted for 10 y to develop the process for recovery, concentration, and localization of U, Pu, Np, Tc, and Zr within 1st extraction cycle. Actinides are recovered from high-level raffinate of this cycle after evaporation and feed adjustment. Results in this report show that combined deep recovery of several elements from highly irradiated materials by TBP extraction, for further transmutation, is possible. Selective stripping of Zr from solvent phase containing U, Pu, Np, and Tc is quite effective. Development of the modified Purex process is not complete; main problem to be solved should be oxide separation from the loop and permissible storage duration before reprocessing and reuse in the loop.

  6. Transmutation of ABO4 compounds incorporating technetium-99 and caesium-137

    Science.gov (United States)

    Kuo, E. Y.; Qin, M. J.; Thorogood, G. J.; Huai, P.; Ren, C. L.; Lumpkin, G. R.; Middleburgh, S. C.

    2017-02-01

    The stability of a series of {AB}{{{O}}}4 minerals incorporating radioactive {}99{Tc} during the latter’s β-decay to {}99{Ru} was investigated theoretically using density functional theory (DFT) computations. The compounds investigated were {{KTcO}}4, {{RbTcO}}4 and {{CsTcO}}4. The stability of the latter, {{CsTcO}}4, during transmutation, when the caesium consists of the radioactive isotope {}137{Cs}, was also investigated. For each of the compounds, two similar possible crystal structure types—scheelite and pseudoscheelite—were considered. As the {}99{Tc} decays, or the {}137{Cs} decays to {}137{Ba}, reaction enthalpies were calculated for possible decompositions or precipitations of the transmuting compounds. All the possible decompositions or precipitations investigated had positive reaction enthalpies, suggesting that the transmuting compounds are all chemically stable. Volume and lattice parameter changes, however, suggest that {{KTcO}}4 would also be structurally stable during transmutation to {{KRuO}}4, but that {{CsTcO}}4 would not be structurally stable during its transmutation to {{BaRuO}}4.

  7. Partitioning and transmutation. Current developments - 2004. A report from the Swedish reference group on P and T-research

    Energy Technology Data Exchange (ETDEWEB)

    Ahlstroem, Per-Eric (ed.) [Swedish Nuclear Fuel and Waste Management Co., Stockholm (Sweden); Andersson, Sofie; Ekberg, Christian; Liljenzin, Jan-Olov; Nilsson, Mikael; Skarnemark, Gunnar [Chalmers Univ. of Technology, Goeteborg (Sweden); Blomgren, Jan [Uppsala Univ. (Sweden). Dept. of Neutron Research; Eriksson, Marcus; Gudowski, Waclaw; Seltborg, Per; Wallenius, Jan; Sehgal, Bal Raj [Royal Inst. of Technology, Stockholm (Sweden)

    2004-05-01

    This report summarises the work reported in the years 1998-2003 and tries to assess the prospects for future development of partitioning and transmutation (P-T) as seen from a Swedish perspective. The R and D efforts on P-T have increased somewhat during the period 1998-2003. Research on P-T has taken a prominent role internationally in the R and D on future nuclear power and nuclear fuel cycle systems. Despite the fact that partitioning and transmutation have been on the agenda for quite a few years there are still a number of issues that must be settled before the research and development can be given a clearly focused direction. Studies propose research programmes for about six years at the cost of a couple of hundred million Euros. The construction of a small ADS experimental plant is a necessary step to develop and demonstrate the concept. This experimental plant should then be followed by a demonstration plant in almost full scale. Such a plant can at the earliest be ready in the mid-2030s. A number of circumstances have, however, contributed to slower speed, less intensity and lower funding than proposed in the studies. There is no unanimous view on the objectives for partitioning and transmutation. Many see it as a way to achieve broad acceptance for nuclear power at large. Others promote it as a way to get out of the impasse for a deep repository in several countries. Others again put a strong emphasise on the proliferation aspects. There is no unanimous view on the need to develop ADS or for the role of ADS in a P-T-system. Some advocate that ADS should be used for burning of all transuranium nuclides from the present enriched uranium fuelled light water reactors. Others see the ADS as a supplement particularly suitable for burning minor actinides (americium, curium and neptunium), whereas the major part of the plutonium should be burned in light water reactors (or in fast reactors) There is no consensus among experts on which technical route to follow

  8. Uniform fabrication of Ge nanocrystals embedded into SiO2 film via neutron transmutation doping

    Directory of Open Access Journals (Sweden)

    Wei Liu

    2014-06-01

    Full Text Available Nanocrystalline 74Ge embedded SiO2 films were prepared by employing ion implantation and neutron transmutation doping methods. Transmission electron microscopy, energy dispersive x-ray spectroscopy, and photoluminescence of the obtained samples were measured. The existence of As dopants transmuted from 74Ge is significant to guarantee the uniformity and higher volume density of Ge nanocrystals by tuning the system׳s crystallinity and activating mass transfer process. It was observed that the photoluminescence intensity of Ge nanocrystals increased first then decreased with the increase of arsenic concentration. The optimized fluence of neutron transmutation doping was found to be 5.5×1017 cm−2 to achieve maximum photoluminescence emission in Ge embedded SiO2 film. This work opens a route in the three-dimensional nanofabrication of uniform Ge nanocrystals.

  9. Fractional calculus transmutation for the Airy WKB solutions and Stokes phenomenon

    Science.gov (United States)

    Kiryakova, Virginia

    2016-12-01

    We apply the transmutation method to give a new explanation of the Stokes phenomenon for the Airy differential equation and of the change of the coeffcients in its asymptotic solutions for large values of argument in different parts of the complex plane. As a transmutation operator, a Weyl type fractional order integral is used. But this scheme is a special case of the so-called Poisson- Sonine-Dimovski transmutation operators related to the hyper-Bessel differential equations of arbitrary integer order, and of the generalized fractional calculus operators related to differential equations of fractional multi-order and their solutions, including a number of special functions. We analyze also the previous results of other authors and suggest some perspectives to use the same method in more general cases.

  10. Transmutation studies using SSNTD and radiochemistry and the associated production of secondary neutrons

    CERN Document Server

    Brandt, R; Wan, J S; Schmidt, T; Langrock, E J; Vater, P; Adam, J; Bamblevski, V P; Bradnova, V; Gelovani, L K; Kalinnikov, V K; Krivopustov, M I; Kulakov, B A; Sosnin, A N; Perelygin, V P; Pronskikh, V S; Stegailov, V I; Tsoupko-Sitnikov, V M; Modolo, G; Odoj, R; Philippen, P W; Adloff, J C; Pape, F; Debeauvais, M; Zamani-Valassiadou, M; Hashemi-Nezhad, S R; Dwivedi, K K; Guo Shi Lun; Li, L; Wang, Y L; Wilson, B

    1999-01-01

    Experiments using 1.5 GeV, 3.7 GeV and 7.4 GeV protons from the Synchrophasotron, LHE, JINR, Dubna, Russia, on extended Pb- and U- targets were carried out using SSNTD and radiochemical sensors for the study of secondary neutron $9 fluences. We also carried out first transmutation studies on the long-lived radwaste nuclei /sup 129/I and /sup 237/Np. In addition, we carried out computer code simulation studies on these systems using LAHET and DCM/CEM codes. We $9 have difficulties to understand rather large transmutation rates observed experimentally when they are compared with computer simulations. There seems to be a rather fundamental problem understanding the large transmutation rates as $9 observed experimentally in Dubna and CERN, as compared to those theoretical computer simulations mentioned above. (10 refs).

  11. Uniform fabrication of Ge nanocrystals embedded into SiO2 film via neutron transmutation doping

    Institute of Scientific and Technical Information of China (English)

    Wei Liu; Tiecheng Lu; Qingyun Chen; Youwen Hu; Shaobo Dun; Issai Shlimak

    2014-01-01

    Nanocrystalline 74Ge embedded SiO2 films were prepared by employing ion implantation and neutron transmutation doping methods. Transmission electron microscopy, energy dispersive x-ray spectroscopy, and photoluminescence of the obtained samples were measured. The existence of As dopants transmuted from 74Ge is significant to guarantee the uniformity and higher volume density of Ge nanocrystals by tuning the system's crystallinity and activating mass transfer process. It was observed that the photoluminescence intensity of Ge nanocrystals increased first then decreased with the increase of arsenic concentration. The optimized fluence of neutron transmutation doping was found to be 5.5 ? 1017 cm ? 2 to achieve maximum photoluminescence emission in Ge embedded SiO2 film. This work opens a route in the three-dimensional nanofabrication of uniform Ge nanocrystals.

  12. Multi-pass Monte Carlo simulation method in nuclear transmutations.

    Science.gov (United States)

    Mateescu, Liviu; Kadambi, N Prasad; Ravindra, Nuggehalli M

    2016-12-01

    Monte Carlo methods, in their direct brute simulation incarnation, bring realistic results if the involved probabilities, be they geometrical or otherwise, remain constant for the duration of the simulation. However, there are physical setups where the evolution of the simulation represents a modification of the simulated system itself. Chief among such evolving simulated systems are the activation/transmutation setups. That is, the simulation starts with a given set of probabilities, which are determined by the geometry of the system, the components and by the microscopic interaction cross-sections. However, the relative weight of the components of the system changes along with the steps of the simulation. A natural measure would be adjusting probabilities after every step of the simulation. On the other hand, the physical system has typically a number of components of the order of Avogadro's number, usually 10(25) or 10(26) members. A simulation step changes the characteristics for just a few of these members; a probability will therefore shift by a quantity of 1/10(25). Such a change cannot be accounted for within a simulation, because then the simulation should have then a number of at least 10(28) steps in order to have some significance. This is not feasible, of course. For our computing devices, a simulation of one million steps is comfortable, but a further order of magnitude becomes too big a stretch for the computing resources. We propose here a method of dealing with the changing probabilities, leading to the increasing of the precision. This method is intended as a fast approximating approach, and also as a simple introduction (for the benefit of students) in the very branched subject of Monte Carlo simulations vis-à-vis nuclear reactors. Copyright © 2016 Elsevier Ltd. All rights reserved.

  13. Capability approach

    DEFF Research Database (Denmark)

    Jensen, Niels Rosendal; Kjeldsen, Christian Christrup

    Lærebogen er den første samlede danske præsentation af den af Amartya Sen og Martha Nussbaum udviklede Capability Approach. Bogen indeholder en præsentation og diskussion af Sen og Nussbaums teoretiske platform. I bogen indgår eksempler fra såvel uddannelse/uddannelsespolitik, pædagogik og omsorg....

  14. ENTREPRENEURIAL CAPABILITIES

    DEFF Research Database (Denmark)

    Rasmussen, Lauge Baungaard; Nielsen, Thorkild

    2003-01-01

    The aim of this article is to analyse entrepreneurship from an action research perspective. What is entrepreneurship about? Which are the fundamental capabilities and processes of entrepreneurship? To answer these questions the article includes a case study of a Danish entrepreneur and his networks...

  15. Study of the distribution of actinides in human tissues using synchrotron radiation micro X-ray fluorescence spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Vergucht, Eva; Samber, Bjoern de; Izmer, Andrei; Vekemans, Bart; Vincze, Laszlo; Vanhaecke, Frank [Ghent Univ. (Belgium). Dept. of Analytical Chemistry; Appel, Karen [DESY-Photo Science, Hamburg (Germany); Tolmachev, Sergei [Washington State Univ., Richland WA (United States). College of Pharmacy

    2015-02-15

    This study aims at evaluating the capabilities of synchrotron radiation micro X-ray fluorescence spectrometry (SR micro-XRF) for qualitative and semi-quantitative elemental mapping of the distribution of actinides in human tissues originating from individuals with documented occupational exposure. The investigated lymph node tissues were provided by the United States Transuranium and Uranium Registries (USTUR) and were analyzed following appropriate sample pre-treatment. Semi-quantitative results were obtained via calibration by external standards and demonstrated that the uranium concentration level in the detected actinide hot spots reaches more than 100 μg/g. For the plutonium hot spots, concentration levels up to 31 μg/g were found. As illustrated by this case study on these unique samples, SR micro-XRF has a high potential for this type of elemental bio-imaging owing to its high sensitivity, high spatial resolution, and non-destructive character.

  16. Transmutation-induced embrittlement of V-Ti-Ni and V-Ni alloys in HFIR

    Energy Technology Data Exchange (ETDEWEB)

    Ohnuki, S.; Takahashi, H. [Hokkaido Univ., Sapparo (Japan); Garner, F.A. [Pacific Northwest National Laboratory, Richland, WA (United States); Pawel, J.E. [Oak Ridge National Laboratory, TN (United States)] [and others

    1996-04-01

    Vanadium, V-1Ni, V-10Ti and V-10Ti-1Ni (at %) were irradiated in HFIR to doses ranging from 18 to 30 dpa and temperatures between 300 and 600C. Since the irradiation was conducted in a highly thermalized neutron spectrum without shielding against thermal neutrons, significant levels of chromium (15-22%) were formed by transmutation. The addition of such large chromium levels strongly elevated the ductile to brittle transition temperature. At higher irradiation temperatures radiation-induced segregation of transmutant Cr and solute Ti at specimen surfaces leads to strong increases in the density of the alloy.

  17. Application of activation methods on the Dubna experimental transmutation set-ups.

    Science.gov (United States)

    Stoulos, S; Fragopoulou, M; Adloff, J C; Debeauvais, M; Brandt, R; Westmeier, W; Krivopustov, M; Sosnin, A; Papastefanou, C; Zamani, M; Manolopoulou, M

    2003-02-01

    High spallation neutron fluxes were produced by irradiating massive heavy targets with proton beams in the GeV range. The experiments were performed at the Dubna High Energy Laboratory using the nuclotron accelerator. Two different experimental set-ups were used to produce neutron spectra convenient for transmutation of radioactive waste by (n,x) reactions. By a theoretical analysis neutron spectra can be reproduced from activation measurements. Thermal-epithermal and fast-super-fast neutron fluxes were estimated using the 197Au, 238U (n,gamma) and (n,2n) reactions, respectively. Depleted uranium transmutation rates were also studied in both experiments.

  18. Calculation and measurement of helium generation and solid transmutations in Cu-Zn-Ni alloys

    Energy Technology Data Exchange (ETDEWEB)

    Greenwood, L.R.; Oliver, B.M.; Garner, F.A. [Pacific Northwest National Lab., Richland, WA (United States); Muroga, T. [National Inst. of Fusion Science, Nagoya (Japan)

    1998-03-01

    A method was recently proposed by Garner and Greenwood that would allow the separation of the effects of solid and gaseous transmutation for Cu-Zn-Ni alloys. Pure copper produces zinc and nickel during neutron irradiation. {sup 63}Cu transmutes to {sup 64}Ni and {sup 64}Zn, in about a 2-to-1 ratio, and {sup 65}Cu transmutes to {sup 66}Zn. The {sup 64}Zn further transmutes to {sup 65}Zn which has been shown to have a high thermal neutron (n,{alpha}) cross-section. Since a three-step reaction sequence is required for natural copper, the amount of helium produced is much smaller than would be produced for the two-step, well-known {sup 58}Ni (n,{gamma}) {sup 59}Ni (n,{alpha}) reaction sequence. The addition of natural Zn and Ni to copper leads to greatly increased helium production in neutron spectra with a significant thermal component. Using a suitable Cu-Zn-Ni alloy matrix and comparative irradiation of thermal neutron-shielded and unshielded specimens, it should be possible to distinguish the separate influences of the solid and gaseous transmutants. Whereas helium generation rates have been previously measured for natural nickel and copper, they have not been measured for natural Zn or Cu-Ni-Zn alloys. The (N,{alpha}) cross section for {sup 65}Zn was inferred from helium measurements made with natural copper. By comparing helium production in Cu and Cu-Zn alloys, this cross section can be determined more accurately. In the current study, both the solid and helium transmutants were measured for Cu, Cu-5Ni, Cu-3.5Zn and Cu-5Ni-2Zn, irradiated in each of two positions in the HFIR JP-23 test. Highly accurate helium measurements were performed on these materials by isotope dilution mass spectrometry using a facility that was recently moved from Rockwell International to PNNL. It is shown that both the helium and solid transmutants for Cu-zn-Ni alloys can be calculated with reasonable certainty, allowing the development of a transmutation experiment as proposed by

  19. Dynamic capabilities

    DEFF Research Database (Denmark)

    Grünbaum, Niels Nolsøe; Stenger, Marianne

    2013-01-01

    and profitability of small and medium sized manufacturing enterprises operating in volatile environments. A multi-case study design was adopted as research strategy. The findings reveal a positive relationship between dynamic capabilities and innovation performance in the case companies, as we would expect. It was...... it was dominated by a lack of systematism, assessment, monitoring, marketing speculations and feasibility calculation. Furthermore, the sphere was dictated by asymmetric supplier-customer relationships and negotiation power leading, among other possible factors, to meager profitability....

  20. Electrochemical decontamination system for actinide processing gloveboxes

    Energy Technology Data Exchange (ETDEWEB)

    Wedman, D.E.; Lugo, J.L.; Ford, D.K.; Nelson, T.O.; Trujillo, V.L.; Martinez, H.E.

    1998-03-01

    An electrolytic decontamination technology has been developed and successfully demonstrated at Los Alamos National Laboratory (LANL) for the decontamination of actinide processing gloveboxes. The technique decontaminates the interior surfaces of stainless steel gloveboxes utilizing a process similar to electropolishing. The decontamination device is compact and transportable allowing it to be placed entirely within the glovebox line. In this way, decontamination does not require the operator to wear any additional personal protective equipment and there is no need for additional air handling or containment systems. Decontamination prior to glovebox decommissioning reduces the potential for worker exposure and environmental releases during the decommissioning, transport, and size reduction procedures which follow. The goal of this effort is to reduce contamination levels of alpha emitting nuclides for a resultant reduction in waste level category from High Level Transuranic (TRU) to low Specific Activity (LSA, less than or equal 100 nCi/g). This reduction in category results in a 95% reduction in disposal and disposition costs for the decontaminated gloveboxes. The resulting contamination levels following decontamination by this method are generally five orders of magnitude below the LSA specification. Additionally, the sodium sulfate based electrolyte utilized in the process is fully recyclable which results in the minimum of secondary waste. The process bas been implemented on seven gloveboxes within LANL`s Plutonium Facility at Technical Area 55. Of these gloveboxes, two have been discarded as low level waste items and the remaining five have been reused.

  1. Stability of artificial ferrite garnets with actinides and lanthanoids in water solutions

    Science.gov (United States)

    Livshits, T. S.

    2008-12-01

    Extraction of the actinide-REE fraction and its subsequent incorporation into sparingly soluble crystalline phases (confinement matrices) is assumed in processing of spent nuclear fuel from high-level radioactive wastes (HLW). The chemical stability in the process of interaction with subsurface water governs the capability of a matrix phase to keep radionuclides from getting into the biosphere. In static experiments at 90 and 150°C, the chemical stability of ferrite garnets was investigated for three compositions with Th4+, Ce4+ and Gd3+ + serving as simulator components of the actinide fraction of HLW. Experiments were carried out in distilled water (pH 6.5), 0.01 M HCl solution (pH 2), and 0.01 M NaOH solution (pH 12). The behavior of ferrigarnet matrices depends on the acidity of the solution. In neutral and alkaline media, Th, Ce, and Gd are virtually not transferred into the liquid phase. Acid leaching promotes intense dissolution of garnet matrices. In this case, the leaching rate of Gd and Th from ceramics into the liquid phase is two orders of magnitude lower than the leaching rate of Ce because the Ce-doped phases contain less stable (relative to garnet) Ce-rich perovskite. Amorphization of the ferrigarnet structure due to 244Cm isotope decay leads to an increase in the leaching rate of Cm by no more than five times. In terms of radiation and chemical stability, ferrite garnets are not inferior to zirconolites and titanate pyrochlores. The experimental results suggest that garnet matrices can reliably immobilize actinides in subsurface repositories.

  2. Studies on Neutron, Photon (Bremsstrahlung and Proton Induced Fission of Actinides and Pre-Actinides

    Directory of Open Access Journals (Sweden)

    H. Naik

    2015-08-01

    Full Text Available We present the yields of various fission products determined in the reactor neutron, 3.7-18.1 MeV quasi-mono energetic neutron, 8-80 MeV bremsstrahlung and 20-45 MeV proton induced fission of 232Th and 238U using radiochemical and off-line beta or gamma ray counting. The yields of the fission products in the bremsstrahlung induced fission natPb and 209Bi with 50- 70 MeV and 2.5 GeV based on off-line gamma ray spectrometric technique were also presented. From the yields of fission products, the mass chains yields were obtained using charge distribution correction. From the mass yield distribution, the peak-to-valley (P/V ratio was obtained. The role of excitation energy on the peak-to-valley ratio and fine structure such as effect of shell closure proximity and even-odd effect of mass yield distribution were examined. The higher yields of the fission products around A=133-134, 138-140 and 143-144 and their complementary products explained from the nuclear structure effect and role of standard I and II mode of asymmetric fission. In the neutron, photon (bremsstrahlung and proton induced fission, the asymmetric mass distribution for actinides (Th, U and symmetric distribution for pre-actinides (Pb, Bi were explained from different type of potential fission barrier

  3. Photofission of actinide and pre-actinide nuclei in the quasideuteron and delta energy regions

    CERN Document Server

    Berman, B L; Cole, P L; Dodge, W R; Feldman, G; Sanabria, J C; Kolb, N; Pywell, R E; Vogt, J; Nedorezov, V; Sudov, A; Kezerashvili, G Ya

    1999-01-01

    The photofission cross sections for the actinide nuclei sup 2 sup 3 sup 2 Th, sup 2 sup 3 sup 3 sup , sup 2 sup 3 sup 5 sup , sup 2 sup 3 sup 8 U, and sup 2 sup 3 sup 7 Np have been measured from 68 to 264 MeV and those for the pre-actinide nuclei sup 1 sup 9 sup 7 Au and sup N sup A sup T Pb from 122 to 222 MeV at the Saskatchewan Accelerator Laboratory, using monoenergetic tagged photons and novel parallel-plate avalanche detectors for the fission fragments. The aim of the experiment was to obtain a comprehensive and self-consistent data set and to investigate previous anomalous results in this energy region. The fission probability for transuranic nuclei is expected to be close to unity here. However, important discrepancies have been confirmed for sup 2 sup 3 sup 7 Np and sup 2 sup 3 sup 2 Th, compared with sup 2 sup 3 sup 8 U, which have serious implications for the inferred total photoabsorption strengths, and hence call into question the 'Universal Curve' for photon absorption at these energies. High-s...

  4. Potential radiation dose from eating fish exposed to actinide contamination

    Energy Technology Data Exchange (ETDEWEB)

    Emery, R.M.; Klopfer, D.C.; Baker, D.A.; Soldat, J.K.

    1980-01-01

    The purpose of this work is to establish a maximum potential for transporting actinides to man via fish consumption. The study took place in U-Pond, a nuclear waste pond on the Hanford Site. It has concentrations of /sup 238/U, /sup 238/Pu, /sup 239,240/Pu and /sup 241/Am that are approximately three orders of magnitude greater than background levels. Fish living in the pond contain higher actinide concentrations than those observed in fish from any other location. Experiments were performed in U-pond to determine maximum quantities of actinides that could accumulate in fillets and whole bodies of two centrarchid fish species. Doses to hypothetical consumers were then estimated by assuming that actinide behavior in their bodies was similar to that defined for Standard Man by the International Commission on Radiological Protection. Results indicate that highest concentrations occurring in bluegill or bass muscle after more than a year's exposure to the pond would not be sufficient to produce a significant radiation dose to a human consumer, even if he ate 0.5 kg (approx.1 lb) of these fillets every day for 70 years. Natural predators (heron or coyote), having lifetime diets of whole fish from U-Pond, would receive less radiation dose from the ingested actinides than from natural background sources. 34 refs., 5 figs., 4 tabs.

  5. Development of the Chalmers Grouped Actinide Extraction Process

    Directory of Open Access Journals (Sweden)

    Halleröd Jenny

    2015-12-01

    Full Text Available Several solvents for Grouped ActiNide EXtraction (GANEX processes have been investigated at Chalmers University of Technology in recent years. Four different GANEX solvents; cyclo-GANEX (CyMe4- -BTBP, 30 vol.% tri-butyl phosphate (TBP and cyclohexanone, DEHBA-GANEX (CyMe4-BTBP, 20 vol.% N,N-di-2(ethylhexyl butyramide (DEHBA and cyclohexanone, hexanol-GANEX (CyMe4-BTBP, 30 vol.% TBP and hexanol and FS-13-GANEX (CyMe4-BTBP, 30 vol.% TBP and phenyl trifluoromethyl sulfone (FS-13 have been studied and the results are discussed and compared in this work. The cyclohexanone based solvents show fast and high extraction of the actinides but a somewhat poor diluent stability in contact with the acidic aqueous phase. FS-13-GANEX display high separation factors between the actinides and lanthanides and a good radiolytic and hydrolytic stability. However, the distribution ratios of the actinides are lower, compared to the cyclohexanone based solvents. The hexanol-GANEX is a cheap solvent system using a rather stable diluent but the actinide extraction is, however, comparatively low.

  6. The actinides-a beautiful ending of the Periodic Table

    Energy Technology Data Exchange (ETDEWEB)

    Johansson, Boerje [Condensed Matter Theory Group, Department of Physics, Uppsala University, Box 530, S-751 21 Uppsala (Sweden); Applied Materials Physics, Department of Materials Science and Engineering, Royal Institute of Technology, Brinellvaegen 23, SE-100 44 Stockholm (Sweden)], E-mail: borje.johansson@fysik.uu.se; Li, Sa [Applied Materials Physics, Department of Materials Science and Engineering, Royal Institute of Technology, Brinellvaegen 23, SE-100 44 Stockholm (Sweden); Department of Physics, Virginia Commonwealth University, Richmond, VA 23284 (United States)

    2007-10-11

    The 5f elements, actinides, show many properties which have direct correspondence to the 4f transition metals, the lanthanides. The remarkable similarity between the solid state properties of compressed Ce and the actinide metals is pointed out in the present paper. The {alpha}-{gamma} transition in Ce is considered as a Mott transition, namely, from delocalized to localized 4f states. An analogous behavior is also found for the actinide series, where the sudden volume increase from Pu to Am can be viewed upon as a Mott transition within the 5f shell as a function of the atomic number Z. On the itinerant side of the Mott transition, the earlier actinides (Pa-Pu) show low symmetry structures at ambient conditions; while across the border, the heavier elements (Am-Cf) present the dhcp structure, an atomic arrangement typical for the trivalent lanthanide elements with localized 4f magnetic moments. The reason for an isostructural Mott transition of the f electron in Ce, as opposed to the much more complicated cases in the actinides, is identified. The strange appearance of the {delta}-phase (fcc) in the phase diagram of Pu is another consequence of the border line behavior of the 5f electrons. The path leading from {delta}-Pu to {alpha}-Pu is identified.

  7. Recovery and chemical purification of actinides at JRC, Karlsruhe

    Science.gov (United States)

    Bokelund, H.; Apostolidis, C.; Glatz, J.-P.

    1989-07-01

    The application of actinide elements in research and in technology is many times subject to rather stringent purity requirements; often a nuclear grade quality is specified. The additional possible demand for a high isotopic purity is a special feature in the handling of these elements. The amount of actinide elements contained in or adhering to materials declared as waste should be low for safety reasons and out of economic considerations. The release of transuranium elements to the environment must be kept negligible. For these and for other reasons a keen interest in the separation of actinides from various materials exists, either for a re-use through recycling, or for their safe confinement in waste packages. This paper gives a short review of the separation methods used for recovery and purification of actinide elements over the past years in the European Institute for Transuranium Elements. The methods described here involve procedures based on precipitation, ion exchange or solvent extraction; often used in a combination. The extraction methods were preferably applied in a Chromatographie column mode. The actinide elements purified and/or separated from each other by the above methods include uranium, neptunium, plutonium, americium, curium, and californium. For the various elements the work was undertaken with different aims, ranging from reprocessing and fabrication of nuclear fuels on a kilogramme scale, over the procurement of alpha-free waste, to the preparation of neutron sources of milligramme size.

  8. Hydrophilic actinide complexation studied by solvent extraction radiotracer technique

    Energy Technology Data Exchange (ETDEWEB)

    Rydberg, J. [Chalmers Univ. of Technology, Goeteborg (Sweden). Dept. of Nuclear Chemistry and Radiochemistry Consultant Group, Vaestra Froelunda (Sweden)

    1996-10-01

    Actinide migration in the ground water is enhanced by the formation of water soluble complexes. It is essential to the risk analysis of a wet repository to know the concentration of central atoms and the ligands in the ground water, and the stability of complexes formed between them. Because the chemical behavior at trace concentrations often differ from that at macro concentrations, it is important to know the chemical behavior of actinides at trace concentrations in ground water. One method used for such investigations is the solvent extraction radiotracer (SXRT) technique. This report describes the SXRT technique in some detail. A particular reason for this analysis is the claim that complex formation constants obtained by SXRT are less reliable than results obtained by other techniques. It is true that several difficulties are encountered in the application of SXRT technique to actinide solution, such as redox instability, hydrophilic complexation by side reactions and sorption, but it is also shown that a careful application of the SXRT technique yields results as reliable as by any other technique. The report contains a literature survey on solvent extraction studies of actinide complexes formed in aqueous solutions, particularly by using the organic reagent thenoyltrifluoroacetone (TTA) dissolved in benzene or chloroform. Hydrolysis constants obtained by solvent extraction are listed as well as all actinide complexes studied by SX with inorganic and organic ligands. 116 refs, 11 tabs.

  9. Plutonium and Minor Actinide Management in Thermal High-Temperature Gas-Cooled Reactors. Publishable Final Activity Report

    Energy Technology Data Exchange (ETDEWEB)

    Kuijper, J.C., E-mail: kuijper@nrg.eu [Nuclear Research and Consultancy Group (NRG), Petten (Netherlands); Somers, J.; Van Den Durpel, L.; Chauvet, V.; Cerullo, N.; Cetnar, J.; Abram, T.; Bakker, K.; Bomboni, E.; Bernnat, W.; Domanska, J.G.; Girardi, E.; De Haas, J.B.M.; Hesketh, K.; Hiernaut, J.P.; Hossain, K.; Jonnet, J.; Kim, Y.; Kloosterman, J.L.; Kopec, M.; Murgatroyd, J.; Millington, D.; Lecarpentier, D.; Lomonaco, G.; McEachern, D.; Meier, A.; Mignanelli, M.; Nabielek, H.; Oppe, J.; Petrov, B.Y.; Pohl, C.; Ruetten, H.J.; Schihab, S.; Toury, G.; Trakas, C.; Venneri, F.; Verfondern, K.; Werner, H.; Wiss, T.; Zakova, J.

    2010-11-15

    The PUMA project -the acronym stands for 'Plutonium and Minor Actinide Management in Thermal High-Temperature Gas-Cooled Reactors'- was a Specific Targeted Research Project (STREP) within the EURATOM 6th Framework Program (EU FP6). The PUMA project ran from September 1, 2006, until August 31, 2009, and was executed by a consortium of 14 European partner organisations and one from the USA. This report serves 2 purposes. It is both the 'Publishable Final Activity Report' and the 'Final (Summary) Report', describing, per Work Package, the specific objectives, research activities, main conclusions, recommendations and supporting documents. PUMA's main objective was to investigate the possibilities for the utilisation and transmutation of plutonium and especially minor actinides in contemporary and future (high temperature) gas-cooled reactor designs, which are promising tools for improving the sustainability of the nuclear fuel cycle. This contributes to the reduction of Pu and MA stockpiles, and also to the development of safe and sustainable reactors for CO{sub 2}-free energy generation. The PUMA project has assessed the impact of the introduction of Pu/MA-burning HTRs at three levels: fuel and fuel performance (modelling), reactor (transmutation performance and safety) and reactor/fuel cycle facility park. Earlier projects already indicated favourable characteristics of HTRs with respect to Pu burning. So, core physics of Pu/MA fuel cycles for HTRs has been investigated to study the CP fuel and reactor characteristics and to assure nuclear stability of a Pu/MA HTR core, under both normal and abnormal operating conditions. The starting point of this investigation comprised the two main contemporary HTR designs, viz. the pebble-bed type HTR, represented by the South-African PBMR, and hexagonal block type HTR, represented by the GT-MHR. The results (once again) demonstrate the flexibility of the contemporary (and near future) HTR

  10. Ventilation system of actinides handling facility in Oarai-branch of Tohoku University

    Energy Technology Data Exchange (ETDEWEB)

    Suzuki, Yoshimitsu; Watanabe, Makoto; Hara, Mituo; Shikama, Tatsuo; Kayano, Hideo; Mitsugashira, Toshiaki [Oarai Branch, Institute for Materials Research, Tohoku Univ., Oarai, Ibaraki (Japan)

    1999-09-01

    We have reported the development of the facility for handling actinides in Tohoku University at the second KAERI-JAERI joint seminar on PIE technology. Actinide isotopes have most hazurdous {alpha}-radioactivity. Therefore, a specially designed facility is necessary to carry out experimental study for actinide physics and chemistry. In this paper, we will describe the ventilation system and monitoring system for actinide handling facility. (author)

  11. Advanced separation and transmutation, long dated behavior of vitrified wastes: 15 years of scientific researches; Separation poussee et transmutation, comportement a long terme des dechets vitrifies: 15 ans d'avancees scientifiques

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2006-02-15

    This report presents the results after 15 years of researches at the Cea, concerning the separation and transmutation of radioactive wastes and the conditioning and the long time storage of wastes at the surface. These researches were asked in the framework of the Bataille law. The first part devoted to the transmutation and separation of ling life radioactive elements presents the challenges, the advanced separation, the transmutation and the evaluation of the researches. The second part devoted to the long dated storage discusses the high activity wastes vitrification, the behavior of the vitrified wastes packages after thousand years, the international researches and the evaluation of the researches. (A.L.B.)

  12. Scent Transmutation: A New Way to Teach on Chemical Equilibrium, Distillation, and Dynamic Combinatorial Chemistry

    Science.gov (United States)

    Ji, Qing; El-Hamdi, Nadia S.; Miljanic´, Ognjen S?.

    2014-01-01

    Esters are volatile and pleasantly smelling compounds, commonly used as food additives. Using Ti(OBu)[subscript 4]-catalyzed acyl exchange, we demonstrate a scent transmutation experiment, in which two fragrant esters swap their acyl and alkoxy substituents and are, during the course of a reactive distillation, quantitatively converted into two…

  13. System and safety studies of accelerator driven transmutation systems. Annual report 1998

    Energy Technology Data Exchange (ETDEWEB)

    Wallenius, J.; Gudowski, W.; Carlsson, Johan; Eriksson, Marcus; Tucek, K. [Royal Inst. of Tech., Stockholm (Sweden). Dept. of Nuclear and Reactor Physics

    1998-12-01

    This annual report describes the accelerator-driven transmutation project conducted at the Department of Nuclear and Reactor Physics at the Royal Institute of Technology. The main results are: development of the simulation tools for accelerator-driven transmutation calculations including an integrated Monte-Carlo burnup module and improvements of neutron energy fission yield simulations, processing of the evacuated nuclear data files including preparation of the temperature dependent neutron cross-sections, development of nuclear data for a medium energy range for some isotopes, development of the models and codes for radiation damage simulations, system studies for the spent fuel transmuter, based on heavy metal coolant and advanced nuclear fuel, contribution to the spallation target design being manufactured in IPPE, Obninsk, and accelerator reliability studies. Moreover a lot of efforts were put to further develop existing international collaboration with the most active research groups in the world together with educational activities in Sweden including a number of meetings and workshops and a graduate course in transmutation. This project has been conducted in close collaboration with the EU-project `Impact of the accelerator based technologies on nuclear fission safety` - IABAT and in bilateral cooperation with different foreign research groups 31 refs, 23 figs

  14. Scent Transmutation: A New Way to Teach on Chemical Equilibrium, Distillation, and Dynamic Combinatorial Chemistry

    Science.gov (United States)

    Ji, Qing; El-Hamdi, Nadia S.; Miljanic´, Ognjen S?.

    2014-01-01

    Esters are volatile and pleasantly smelling compounds, commonly used as food additives. Using Ti(OBu)[subscript 4]-catalyzed acyl exchange, we demonstrate a scent transmutation experiment, in which two fragrant esters swap their acyl and alkoxy substituents and are, during the course of a reactive distillation, quantitatively converted into two…

  15. Fluoride-conversion synthesis of homogeneous actinide oxide solid solutions

    Energy Technology Data Exchange (ETDEWEB)

    Silva, G W Chinthaka M [ORNL; Hunn, John D [ORNL; Yeamans, Charles B. [University of California, Berkeley; Cerefice, Gary S. [University of Nevada, Las Vegas; Czerwinski, Ken R. [University of Nevada, Las Vegas

    2011-01-01

    Here, a novel route to synthesize (U, Th)O2 solid solutions at a relatively low temperature of 1100 C is demonstrated. First, the separate actinide oxides reacted with ammonium bifluoride to form ammonium actinide fluorides at room temperature. Subsequently, this mixture was converted to the actinide oxide solid solution using a two-phased heat treatment, first at 610 C in static air, then at 1100 C in flowing argon. Solid solutions obeying Vegard s Law were synthesized for ThO2 content from 10 to 90 wt%. Microscopy showed that the (U, Th)O2 solid solutions synthesized with this method to have considerably high crystallinity and homogeneity, suggesting the suitability of material thus synthesized for sintering into nuclear fuel pellets at low temperatures.

  16. Actinide (III) solubility in WIPP Brine: data summary and recommendations

    Energy Technology Data Exchange (ETDEWEB)

    Borkowski, Marian; Lucchini, Jean-Francois; Richmann, Michael K.; Reed, Donald T.

    2009-09-01

    The solubility of actinides in the +3 oxidation state is an important input into the Waste Isolation Pilot Plant (WIPP) performance assessment (PA) models that calculate potential actinide release from the WIPP repository. In this context, the solubility of neodymium(III) was determined as a function of pH, carbonate concentration, and WIPP brine composition. Additionally, we conducted a literature review on the solubility of +3 actinides under WIPP-related conditions. Neodymium(III) was used as a redox-invariant analog for the +3 oxidation state of americium and plutonium, which is the oxidation state that accounts for over 90% of the potential release from the WIPP through the dissolved brine release (DBR) mechanism, based on current WIPP performance assessment assumptions. These solubility data extend past studies to brine compositions that are more WIPP-relevant and cover a broader range of experimental conditions than past studies.

  17. X-ray and electron microscopy of actinide materials.

    Science.gov (United States)

    Moore, Kevin T

    2010-06-01

    Actinide materials demonstrate a wide variety of interesting physical properties in both bulk and nanoscale form. To better understand these materials, a broad array of microscopy techniques have been employed, including transmission electron microscopy (TEM), electron energy-loss spectroscopy (EELS), energy dispersive X-ray spectroscopy (EDXS), high-angle annular dark-field imaging (HAADF), scanning electron microscopy (SEM), wavelength dispersive X-ray spectroscopy (WDXS), electron back scattered diffraction (EBSD), scanning tunneling microscopy (STM), atomic force microscopy (AFM), and scanning transmission X-ray microscopy (STXM). Here these techniques will be reviewed, highlighting advances made in the physics, materials science, chemistry, and biology of actinide materials through microscopy. Construction of a spin-polarized TEM will be discussed, considering its potential for examining the nanoscale magnetic structure of actinides as well as broader materials and devices, such as those for computational magnetic memory. Copyright 2009 Elsevier Ltd. All rights reserved.

  18. Electronic, structural, and thermodynamic properties of actinide dioxides

    Science.gov (United States)

    Ma, Li; Atta-Fynn, Raymond; Ray, Asok K.

    2010-03-01

    As a continuation of our studies of pure actinide metals using hybrid density functional theory,footnotetextR. Atta-Fynn and A. K. Ray, Europhysics Letters, 85, 27008-p1- p6 (2009); Chemical Physics Letters, 482, 223-227 (2009). we present here a systematic study of the electronic and geometric structure properties of the actinide dioxides, UO2, PuO2 and AmO2, using both density functional and hybrid density functional theories. For the hybrid density functionals, the fractions of exact Hartree-Fock exchange used were 25% and 40%. Each compound has been studied at the nonmagnetic, ferromagnetic and antiferromagnetic configurations, with and without spin-orbit coupling (SOC). The influence of SOC on the properties of the actinide dioxides will be discussed. Thermodynamic properties such as phonon dispersion curves, heat capacity, entropy, internal energy and free energy have been calculated by a coupling of first-principles calculations and lattice dynamics.

  19. Prompt Fission Neutron Spectra of Actinides

    Energy Technology Data Exchange (ETDEWEB)

    Capote, R; Chen, Y J; Hambsch, F J; Kornilov, N V; Lestone, J P; Litaize, O; Morillon, B; Neudecker, D; Oberstedt, S; Ohsawa, T; Smith, D. L.

    2016-01-01

    The energy spectrum of prompt neutrons emitted in fission (PFNS) plays a very important role in nuclear science and technology. A Coordinated Research Project (CRP) “Evaluation of Prompt Fission Neutron Spectra of Actinides”was established by the IAEA Nuclear Data Section in 2009, with the major goal to produce new PFNS evaluations with uncertainties for actinide nuclei. The following technical areas were addressed: (i) experiments and uncertainty quantification (UQ): New data for neutron-induced fission of 233U, 235U, 238U, and 239Pu have been measured, and older data have been compiled and reassessed. There is evidence from the experimental work of this CRP that a very small percentage of neutrons emitted in fission are actually scission neutrons; (ii) modeling: The Los Alamos model (LAM) continues to be the workhorse for PFNS evaluations. Monte Carlo models have been developed that describe the fission phenomena microscopically, but further development is needed to produce PFNS evaluations meeting the uncertainty targets; (iii) evaluation methodologies: PFNS evaluations rely on the use of the least-squares techniques for merging experimental and model data. Considerable insight was achieved on how to deal with the problem of too small uncertainties in PFNS evaluations. The importance of considering that all experimental PFNS data are “shape” data was stressed; (iv) PFNS evaluations: New evaluations, including covariance data, were generated for major actinides including 1) non-model GMA evaluations of the 235U(nth,f), 239Pu(nth,f), and 233U(nth,f) PFNS based exclusively on experimental data (0.02 ≤ E ≤ 10 MeV), which resulted in PFNS average energies E of 2.00±0.01, 2.073±0.010, and 2.030±0.013 MeV, respectively; 2) LAM evaluations of neutron-induced fission spectra on uranium and plutonium targets with improved UQ for incident energies from thermal up to 30 MeV; and 3) Point-by-Point calculations for 232Th, 234U and 237Np targets; and (v) data

  20. Modeling actinide chemistry with ASPEN PLUS

    Energy Technology Data Exchange (ETDEWEB)

    Grigsby, C.O.

    1995-12-31

    When chemical engineers think of chemical processing, they often do not include the US government or the national laboratories as significant participants. Compared to the scale of chemical processing in the chemical process, petrochemical and pharmaceutical industries, the government contribution to chemical processing is not large. However, for the past fifty years, the US government has been, heavily involved in chemical processing of some very specialized materials, in particular, uranium and plutonium for nuclear weapons. Individuals and corporations have paid taxes that, in part have been used to construct and to maintain a series of very expensive laboratories and production facilities throughout the country. Even ignoring the ongoing R & D costs, the price per pound of enriched uranium or of plutonium exceeds that of platinum by a wide margin. Now, with the end of the cold war, the government is decommissioning large numbers of nuclear weapons and cleaning up the legacy of radioactive wastes generated over the last fifty years. It is likely that the costs associated with the build-down and clean-up of the nuclear weapons complex will exceed the investment of the past fifty years of production. Los Alamos National Laboratory occupies a special place in the history of nuclear weapons. The first weapons were designed and assembled at Los Alamos using uranium produced in Oak Ridge, Tennessee or plutonium produced in Richland, Washington. Many of the thermophysical and metallurgical properties of actinide elements have been investigated at Los Alamos. The only plutonium processing facility currently operating in the US is in Los Alamos, and the Laboratory is striving to capture and maintain the uranium processing technology applicable to the post-cold war era. Laboratory researchers are actively involved in developing methods for cleaning up the wastes associated with production of nuclear weapons throughout the US.

  1. In pursuit of homoleptic actinide alkyl complexes.

    Science.gov (United States)

    Seaman, Lani A; Walensky, Justin R; Wu, Guang; Hayton, Trevor W

    2013-04-01

    This Forum Article describes the pursuit of isolable homoleptic actinide alkyl complexes, starting with the pioneering work of Gilman during the Manhattan project. The initial reports in this area suggested that homoleptic uranium alkyls were too unstable to be isolated, but Wilkinson demonstrated that tractable uranium alkyls could be generated by purposeful "ate" complex formation, which serves to saturate the uranium coordination sphere and provide the complexes with greater kinetic stability. More recently, we reported the solid-state molecular structures of several homoleptic uranium alkyl complexes, including [Li(THF)4][U(CH2(t)Bu)5], [Li(TMEDA)]2[UMe6], [K(THF)]3[K(THF)2][U(CH2Ph)6]2, and [Li(THF)4][U(CH2SiMe3)6], by employing Wilkinson's strategy. Herein, we describe our attempts to extend this chemistry to thorium. The treatment of ThCl4(DME)2 with 5 equiv of LiCH2(t)Bu or LiCH2SiMe3 at -25 °C in THF affords [Th(CH2(t)Bu)5] (1) and [Li(DME)2][Th(CH2SiMe3)5 (2), respectively, in moderate yields. Similarly, the treatment of ThCl4(DME)2 with 6 equiv of K(CH2Ph) produces [K(THF)]2[Th(CH2Ph)6] (3), in good yield. Complexes 1-3 have been fully characterized, while the structures of 1 and 3 were confirmed by X-ray crystallography. Additionally, the electronic properties of 1 and 3 were explored by density functional theory.

  2. Actinide consumption: Nuclear resource conservation without breeding

    Energy Technology Data Exchange (ETDEWEB)

    Hannum, W.H.; Battles, J.E.; Johnson, T.R.; McPheeters, C.C.

    1991-01-01

    A new approach to the nuclear power issue based on a metallic fast reactor fuel and pyrometallurgical processing of spent fuel is showing great potential and is approaching a critical demonstration phase. If successful, this approach will complement and validate the LWR reactor systems and the attendant infrastructure (including repository development) and will alleviate the dominant concerns over the acceptability of nuclear power. The Integral Fast Reactor (IFR) concept is a metal-fueled, sodium-cooled pool-type fast reactor supported by a pyrometallurgical reprocessing system. The concept of a sodium cooled fast reactor is broadly demonstrated by the EBR-II and FFTF in the US; DFR and PFR in the UK; Phenix and SuperPhenix in France; BOR-60, BN-350, BN-600 in the USSR; and JOYO in Japan. The metallic fuel is an evolution from early EBR-II fuels. This fuel, a ternary U-Pu-Zr alloy, has been demonstrated to be highly reliable and fault tolerant even at very high burnup (160-180,000 MWd/MT). The fuel, coupled with the pool type reactor configuration, has been shown to have outstanding safety characteristics: even with all active safety systems disabled, such a reactor can survive a loss of coolant flow, a loss of heat sink, or other major accidents. Design studies based on a small modular approach show not only its impressive safety characteristics, but are projected to be economically competitive. The program to explore the feasibility of actinide recovery from spent LWR fuel is in its initial phase, but it is expected that technical feasibility could be demonstrated by about 1995; DOE has not yet committed funds to achieve this objective. 27 refs.

  3. Measurement of Actinides in Molybdenum-99 Solution Analytical Procedure

    Energy Technology Data Exchange (ETDEWEB)

    Soderquist, Chuck Z. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Weaver, Jamie L. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

    2015-11-01

    This document is a companion report to a previous report, PNNL 24519, Measurement of Actinides in Molybdenum-99 Solution, A Brief Review of the Literature, August 2015. In this companion report, we report a fast, accurate, newly developed analytical method for measurement of trace alpha-emitting actinide elements in commercial high-activity molybdenum-99 solution. Molybdenum-99 is widely used to produce 99mTc for medical imaging. Because it is used as a radiopharmaceutical, its purity must be proven to be extremely high, particularly for the alpha emitting actinides. The sample of 99Mo solution is measured into a vessel (such as a polyethylene centrifuge tube) and acidified with dilute nitric acid. A gadolinium carrier is added (50 µg). Tracers and spikes are added as necessary. Then the solution is made strongly basic with ammonium hydroxide, which causes the gadolinium carrier to precipitate as hydrous Gd(OH)3. The precipitate of Gd(OH)3 carries all of the actinide elements. The suspension of gadolinium hydroxide is then passed through a membrane filter to make a counting mount suitable for direct alpha spectrometry. The high-activity 99Mo and 99mTc pass through the membrane filter and are separated from the alpha emitters. The gadolinium hydroxide, carrying any trace actinide elements that might be present in the sample, forms a thin, uniform cake on the surface of the membrane filter. The filter cake is first washed with dilute ammonium hydroxide to push the last traces of molybdate through, then with water. The filter is then mounted on a stainless steel counting disk. Finally, the alpha emitting actinide elements are measured by alpha spectrometry.

  4. Thermally unstable complexants/phosphate mineralization of actinides

    Energy Technology Data Exchange (ETDEWEB)

    Nash, K. [Argonne National Lab., IL (United States)

    1996-10-01

    In situ immobilization is an approach to isolation of radionuclides from the hydrosphere that is receiving increasing attention. Rather than removing the actinides from contaminated soils, this approach transforms the actinides into intrinsically insoluble mineral phases resistant to leaching by groundwater. The principal advangates of this concept are the low cost and low risk of operator exposure and/or dispersion of the radionuclides to the wider environment. The challenge of this approach is toe accomplish the immobilization without causing collateral damage to the environment (the cure shouldn`t be worse than the disease) and verification of system performance.

  5. New cubic structure compounds as actinide host phases

    Energy Technology Data Exchange (ETDEWEB)

    Stefanovsky, S V [SIA Radon, 7th Rostovskii lane 2/14, Moscow 119121 (Russian Federation); Yudintsev, S V; Livshits, T S, E-mail: profstef@mtu-net.ru [Institute of Geology of Ore Deposits, Petrography, Mineralogy and Geochemistry RAS, Staromonetny lane 35, Moscow 119017 (Russian Federation)

    2010-03-15

    Various compounds with fluorite (cubic zirconia) and fluorite-derived (pyrochlore, zirconolite) structures are considered as promising actinide host phases at immobilization of actinide-bearing nuclear wastes. Recently some new cubic compounds - stannate and stannate-zirconate pyrochlores, murataite and related phases, and actinide-bearing garnet structure compounds were proposed as perspective matrices for complex actinide wastes. Zirconate pyrochlore (ideally Gd{sub 2}Zr{sub 2}O{sub 7}) has excellent radiation resistance and high chemical durability but requires high temperatures (at least 1500 deg. C) to be produced by hot-pressing from sol-gel derived precursor. Partial Sn{sup 4+} substitution for Zr{sup 4+} reduces production temperature and the compounds REE{sub 2}ZrSnO{sub 7} may be hot-pressed or cold pressed and sintered at {approx}1400 deg. C. Pyrochlore, A{sub 2}B{sub 2}O{sub 7-x} (two-fold elementary fluorite unit cell), and murataite, A{sub 3}B{sub 6}C{sub 2}O{sub 20-y} (three-fold fluorite unit cell), are end-members of the polysomatic series consisting of the phases whose structures are built from alternating pyrochlore and murataite blocks (nano-sized modules) with seven- (2C/3C/2C), five- (2C/3C), eight- (3C/2C/3C) and three-fold (3C - murataite) fluorite unit cells. Actinide content in this series reduces in the row: 2C (pyrochlore) > 7C > 5C > 8C > 3C (murataite). Due to congruent melting murataite-based ceramics may be produced by melting and the firstly segregated phase at melt crystallization is that with the highest fraction of the pyrochlore modules in its structure. The melts containing up to 10 wt. % AnO{sub 2} (An = Th, U, Np, Pu) or REE/An fraction of HLW form at crystallization zoned grains composed sequentially of the 5C {yields} 8C {yields} 3C phases with the highest actinide concentration in the core and the lowest - in the rim of the grains. Radiation resistance of the 'murataite' is comparable to titanate pyrochlores. One

  6. New molecules for the separation of actinides (III): the picolinamides

    Energy Technology Data Exchange (ETDEWEB)

    Cordier, P.Y.; Condamines, N.; Berthon, L.; Madic, C.

    1994-12-31

    Minor actinide partitioning from high level liquid wastes produced during the reprocessing of nuclear fuels by the Purex process, requires the design of new extracting molecules. These new extractants must be able to separate, for example, actinides from lanthanides. This separation is very difficult, due to the similar chemical properties of these metallic species, but it can possibly be reached by using extractants with soft donor atoms (N or S). Some new molecules : the picolinamides are investigated in this way. The general chemical formula and the behaviour of these compounds in acidic media are given. (O.L.). 3 refs.

  7. Production of heavy actinides in incomplete fusion reactions

    Science.gov (United States)

    Antonenko, N. V.; Cherepanov, E. A.; Iljinov, A. S.; Mebel, M. V.

    1994-10-01

    We present preliminary results of calculations by the phenomenological model of the estimated yield of some heavy actinide isotopes. It is assumed that these isotopes are produced as a result of multinucleon transfers followed by neutrons and charged particle emission A.S. Iljinov and E.A. Cherepanov (1980). The yield P(sub Z, N)(E*) of primary excited actinides is found using the model of N.V. Antonenko and R.V. Jolos (1991). Absolute cross-sections for different binary reaction channels are obtained by summing the cross-sections for all subchannels with an appreciable yield according to J. Wilczynski et al. (1980).

  8. Physics studies of higher actinide consumption in an LMR

    Energy Technology Data Exchange (ETDEWEB)

    Hill, R.N.; Wade, D.C.; Fujita, E.K.; Khalil, H.S.

    1990-01-01

    The core physics aspects of the transuranic burning potential of the Integral Fast Reactor (IFR) are assessed. The actinide behavior in fissile self-sufficient IFR closed cycles of 1200 MWt size is characterized, and the transuranic isotopics and risk potential of the working inventory are compared to those from a once-through LWR. The core neutronic performance effects of rare-earth impurities present in the recycled fuel are addressed. Fuel cycle strategies for burning transuranics from an external source are discussed, and specialized actinide burner designs are described. 4 refs., 4 figs., 3 tabs.

  9. Physics studies of higher actinide consumption in an LMR

    Energy Technology Data Exchange (ETDEWEB)

    Hill, R.N.; Wade, D.C.; Fujita, E.K.; Khalil, H.S.

    1990-01-01

    The core physics aspects of the transuranic burning potential of the Integral Fast Reactor (IFR) are assessed. The actinide behavior in fissile self-sufficient IFR closed cycles of 1200 MWt size is characterized, and the transuranic isotopics and risk potential of the working inventory are compared to those from a once-through LWR. The core neutronic performance effects of rare-earth impurities present in the recycled fuel are addressed. Fuel cycle strategies for burning transuranics from an external source are discussed, and specialized actinide burner designs are described. 4 refs., 4 figs., 3 tabs.

  10. SOLVENT EXTRACTION PROCESS FOR SEPARATING ACTINIDE AND LANTHANIDE METAL VALUES

    Science.gov (United States)

    Hildebrandt, R.A.; Hyman, H.H.; Vogler, S.

    1962-08-14

    A process of countercurrently extracting an aqueous mineral acid feed solution for the separation of actinides from lanthanides dissolved therern is described. The feed solution is made acid-defrcient with alkali metal hydroxide prior to.contact with acid extractant; during extraction, however, acid is transferred from organic to aqueous solution and the aqueous solution gradually becomes acid. The acid-deficient phase ' of the process promotes the extraction of the actinides, while the latter acid phase'' of the process improves retention of the lanthanides in the aqueous solution. This provides for an improved separation. (AEC)

  11. The FIGARO facility at Los Alamos. Capabilities and first results

    Energy Technology Data Exchange (ETDEWEB)

    Haight, Robert; Devlin, Matthew; Zanini, Luca; O' donnell, John [Los Alamos National Laboratory, Los Alamos, NM (United States); Aprahamian, Ani [University of Notre Dame, Notre Dame, IN (United States); Saladin, Juerg [University of Pittsburgh, Pittsburgh, PA (United States)

    2002-08-01

    A new beam line at the fast neutron spallation source at Los Alamos Neutron Science Center has been constructed for studies of neutron-induced reactions producing gamma rays, internal conversion electrons or neutrons. This facility, called FIGARO (Fast neutron-Induced GAmma-Ray Observer), follows on the great successes of GEANIE (described in other contributions to this Conference), by detecting de-excitation gamma rays with high-resolution germanium detectors. FIGARO has fewer gamma-ray detectors than GEANIE, but instead offers other features including: extremely good collimation of the neutron beam for background reduction, a flexible experimental area to optimize detection efficiency and to allow evaluation of other detectors such as ICEBALL-II for internal conversion electrons, inclusion of neutron detectors for the study of neutron-gamma coincidences, beam time to relieve the scheduling pressure on GEANIE, and a PC-based data acquisition system. Our initial measurements include level density studies through {sup 59}Co(n, xgamma) reactions to complement our previous {sup 59}Co(n, xalpha) measurements, reaction studies of MeV neutrons on {sup 99}Tc with the goal of determining cross sections relevant to transmutation and neutron transport in the design of facilities to incinerate nuclear waste, and an assessment of measuring internal conversion electrons, rather than gamma rays, produced by neutron excitation of actinides. (author)

  12. The FIGARO Facility at Los Alamos : capabilities and first results /

    Energy Technology Data Exchange (ETDEWEB)

    Devlin, M. J. (Matthew J.); Zanini, L.; O' Donnell, J. M.; Aprahamian, A. (Ani); Saladin, J. X.; Haight, Robert C.

    2001-01-01

    A new beam line at the fast neutron spallation source at Los Alamos Neutron Science Center has been constructed for studies of neutron-induced reactions producing gamma rays, internal conversion electrons or neutrons. This facility, called FIGARO (Fast neutron-Induced GAmma-Ray Observer), follows on the great successes of GEANIE (described in other contributions to this Conference), by detecting de-excitation gamma rays with high-resolution germanium detectors. FIGARO has fewer gamma-ray detectors than GEANIE, but instead offers other features including: extremely good collimation of the neutron beam for background reduction, a flexible experimental area to optimize detection efficiency and to allow evaluation of other detectors such as ICEBALL-II for internal conversion electrons, inclusion of neutron detectors for the study of neutron-gamma coincidences, beam time to relieve the scheduling pressure on GEANIE, and a PC-based data acquisition system. Our initial measurements include level density studies through 59Co(n,xgamma) reactions to complement our previous 59Co(n,xalpha) measurements, reaction studies of MeV neutrons on 99Tc with the goal of determining cross sections relevant to transmutation and neutron transport in the design of facilities to incinerate nuclear waste, and an assessment of measuring internal conversion electrons, rather than gamma rays, produced by neutron excitation of actinides.

  13. Non-compound nucleus fission in actinide and pre-actinide regions

    Indian Academy of Sciences (India)

    R Tripathi; S Sodaye; K Sudarshan

    2015-08-01

    In this article, some of our recent results on fission fragment/product angular distributions are discussed in the context of non-compound nucleus fission. Measurement of fission fragment angular distribution in 28Si+176Yb reaction did not show a large contribution from the non-compound nucleus fission. Data on the evaporation residue cross-sections, in addition to those on mass and angular distributions, are necessary for better understanding of the contribution from non-compound nucleus fission in the pre-actinide region. Measurement of mass-resolved angular distribution of fission products in 20Ne+232Th reaction showed an increase in angular anisotropy with decreasing asymmetry of mass division. This observation can be explained based on the contribution from pre-equilibrium fission. Results of these studies showed that the mass dependence of anisotropy may possibly be used to distinguish pre-equilibrium fission and quasifission.

  14. The Transmutation of Evolution%进化的转义

    Institute of Scientific and Technical Information of China (English)

    金晓星

    2011-01-01

    Charles Darwin' s influence was not soon felt in China. Modern records of Darwin in China, contained in newspapers, translated works, personal notes and exam papers, began to emerge after the 1870s. Missionaries from abroad and overseas students from China played an important role in the early dissemination of the theory of evolution, although their description of Darwin was generally unclear and not to the point. Yah Fu initiated an era of evolution through his outstanding work, but what filled the newspapers and people' s minds was actually a kind of non-Darwin evolutionary views. The process of the translation of The Origin of Species could roughly be divided into two stages, the first of which is the major concern in this article. Its translation should have brought hope for rectifying the "misunderstanding of evolution", however, Ma Junwu, its translator did not subvert the newly formed evolutionary "mode". By revising the wording in Darwin' s original text, Ma tried to bridge the gap between Darwin' s theory and its previous concepts on evolution which had been instilled in the people of his time. The second part of this article aims to acquire the transmutation of evolutionary thoughts in Ma' s time by analyzing his earlier translation of Chapters III and IV of The Origin of Species.%达尔文的影响力并没有很快抵达中国。近代关于他的记录出现于19世纪70年代之后的译作、报刊、私人笔记或考卷等之中。传教士、留洋人士在早期的传播中扮演了重要角色——尽管他们对于达尔文的介绍常是模糊且不得要领的。严复的杰出工作开启了一个进化的时代,但充斥在报刊和人们思想之中的是一种非达尔文式的进化观念。《物种起源》(下文称《起源》)的翻译大抵可分为两个阶段——本文关注的是第一阶段。《起源》的翻译本可以为纠正“进化的误解”带来希望,然而译者马君武并没有去

  15. 聚变驱动的次临界系统嬗变MA的研究%Minor Actinide Transmutation Analysis of Fusion-Driven Subcritical System

    Institute of Scientific and Technical Information of China (English)

    杨超; 曹良志; 吴宏春; 郑友琦; 祖铁军

    2013-01-01

    一种嬗变次锕系核素(MA)的聚变驱动次临界包层的概念设计被提出.利用MCNP+ ORIGEN2对次临界嬗变包层的能量放大倍数(M)、氚增殖比(TBR)、第一壁负载等中子学参数进行了分析.在保证这些参数满足设计要求的前提下,分析了两种不同的装载方案对MA嬗变能力的影响,最终MA的嬗变率能达24.3%,嬗变支持比为28.研究表明,该聚变驱动次临界嬗变包层能有效嬗变MA.

  16. Molecular and electronic structure of actinide hexa-cyanoferrates; Structure moleculaire et electronique des hexacyanoferrates d'actinides

    Energy Technology Data Exchange (ETDEWEB)

    Bonhoure, I

    2001-07-01

    The goal of this work is to improve our knowledge on the actinide-ligand bond properties. To this end, the hexacyanoferrate entities have been used as pre-organized ligand. We have synthesized, using mild chemistry, the following series of complexes: An{sup IV}[Fe{sup II}(CN){sub 6}].xH{sub 2}O (An = Th, U, Np, Pu); Am{sup III}[Fe{sup III}(CN){sub 6}].xH{sub 2}O; Pu {sup III}[Co{sup III}(CN){sub 6}].xH{sub 2}O and K(H?)An{sup III}[Fe{sup II}(CN){sub 6}].xH{sub 2}O (An = Pu, Am). The metal oxidation states have been obtained thanks to the {nu}{sub CN}, stretching vibration and to the actinide L{sub III} absorption edge studies. As Prussian Blue, the An{sup IV}[Fe{sup II}(CN){sub 6}].xH{sub 2}O (An = Np, Pu) are class II of Robin and Day compounds. X-ray Diffraction has shown besides that these complexes crystallize in the P6{sub 3}/m space group, as the isomorphic LaKFe(CN){sub 6}.4H{sub 2}O complex used as structural model. The EXAFS oscillations at the iron K edge and at the An L{sub III} edge allowed to determine the An-N, An-O, Fe-C and Fe-N distances. The display of the multiple scattering paths for both edges explains the actinide contribution absence at the iron edge, whereas the iron signature is present at the actinide edge. We have shown that the actinide coordination sphere in actinides hexa-cyanoferrates is comparable to the one of lanthanides. However, the actinides typical behavior towards the lanthanides is brought to the fore by the An{sup IV} versus Ln{sup III} ions presence in this family of complexes. Contrarily to the 4f electrons, the 5f electrons influence the electronic properties of the compounds of this family. However, the gap between the An-N and Ln-N distances towards the corresponding metals ionic radii do not show any covalence bond evolution between the actinide and lanthanide series. (author)

  17. Transmutation of nuclear wastes using photonuclear reactions triggered by Compton backscattering photons at the Shanghai laser electrongamma source

    Institute of Scientific and Technical Information of China (English)

    CHEN Jin-Gen; YUAN Ren-Yong; XU Jia-Qiang; YAN Zhe; FAN Gong-Tao; SHEN Wen-Qing; XU Wang; WANG Hong-Wei; GUO Wei; MA Yu-Gang; CAI Xiang-Zhou; LU Guang-Cheng; XU Yi; PAN Qiang-Yan

    2008-01-01

    Based on the facility of the Shanghai Laser Electron Gamma Source (SLEGS),the transmutation for nuclear wastes such as 137Cs and 129I is investigated.It is found that nuclear waste can be transmuted efficiently via photonuclear reaction triggered by gamma photons generated from Compton backscattering between CO2 laser photons and 3.5 GeV electrons.The nuclear activities of 137Cs and 129I are evaluated and compared with the results of transmutation triggered by bremsstrahlung gamma photons driven by ultra intense laser.Due to the better character of gamma photon spectrum as well as the high brightness of gamma photons,the transmutation rate of Compton backscattering method is much higher than that of the bremsstrahlung method.

  18. EASY-II: a system for modelling of n, d, p, γ and α activation and transmutation processes

    Science.gov (United States)

    Sublet, Jean-Christophe; Eastwood, James; Morgan, Guy; Koning, Arjan; Rochman, Dimitri

    2014-06-01

    EASY-II is designed as a functional replacement for the previous European Activation System, EASY-2010. It has extended nuclear data and new software, FISPACT-II, written in object-style Fortran to provide new capabilities for predictions of activation, transmutation, depletion and burnup. The new FISPACT-II code has allowed us to implement many more features in terms of energy range, up to GeV; incident particles: alpha, gamma, proton, deuteron and neutron; and neutron physics: self-shielding effects, temperature dependence, pathways analysis, sensitivity and error estimation using covariance data. These capabilities cover most application needs: nuclear fission and fusion, accelerator physics, isotope production, waste management and many more. In parallel, the maturity of modern general-purpose libraries such as TENDL-2012 encompassing thousands of target nuclides, the evolution of the ENDF format and the capabilities of the latest generation of processing codes PREPRO-2012, NJOY2012 and CALENDF-2010 have allowed the FISPACT-II code to be fed with more robust, complete and appropriate data: cross-sections with covariance, probability tables in the resonance ranges, kerma, dpa, gas and radionuclide production and 24 decay types. All such data for the five most important incident particles are placed in evaluated data files up to an incident energy of 200 MeV. The resulting code and data system, EASY-II, includes many new features and enhancements. It has been extensively tested, and also benefits from the feedback from wide-ranging validation and verification activities performed with its predecessor

  19. Neutronic Assessment of Transmutation Target Compositions in Heterogeneous Sodium Fast Reactor Geometries

    Energy Technology Data Exchange (ETDEWEB)

    Samuel E. Bays; Rodolfo M. Ferrer; Michael A. Pope; Benoit Forget; Mehdi Asgari

    2008-02-01

    The sodium fast reactor is under consideration for consuming the transuranic waste in the spent nuclear fuel generated by light water reactors. This work is concerned with specialized target assemblies for an oxide-fueled sodium fast reactor that are designed exclusively for burning the americium and higher mass actinide component of light water reactor spent nuclear fuel (SNF). The associated gamma and neutron radioactivity, as well as thermal heat, associated with decay of these actinides may significantly complicate fuel handling and fabrication of recycled fast reactor fuel. The objective of using targets is to isolate in a smaller number of assemblies these concentrations of higher actinides, thus reducing the volume of fuel having more rigorous handling requirements or a more complicated fabrication process. This is in contrast to homogeneous recycle where all recycled actinides are distributed among all fuel assemblies. Several heterogeneous core geometries were evaluated to determine the fewest target assemblies required to burn these actinides without violating a set of established fuel performance criteria. The DIF3D/REBUS code from Argonne National Laboratory was used to perform the core physics and accompanying fuel cycle calculations in support of this work. Using the REBUS code, each core design was evaluated at the equilibrium cycle condition.

  20. Surface energy and work function of the light actinides

    DEFF Research Database (Denmark)

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

    1994-01-01

    We have calculated the surface energy and work function of the light actinides Fr, Ra, Ac, Th, Pa, U, Np, and Pu by means of a Green's-function technique based on the linear-muffin-tin-orbitals method within the tight-binding representation. In these calculations we apply an energy functional which...

  1. Experimental Evaluation of Actinide Transport in a Fractured Granodiorite

    Energy Technology Data Exchange (ETDEWEB)

    Dittrich, Timothy M. [Los Alamos National Laboratory; Reimus, Paul W. [Los Alamos National Laboratory

    2015-03-16

    The objective of this study was to demonstrate and evaluate new experimental methods for quantifying the potential for actinide transport in deep fractured crystalline rock formations. We selected a fractured granodiorite at the Grimsel Test Site (GTS) in Switzerland as a model system because field experiments have already been conducted with uranium and additional field experiments using other actinides are planned at the site. Thus, working on this system provides a unique opportunity to compare lab experiment results with fieldscale observations. Rock cores drilled from the GTS were shipped to Los Alamos National Laboratory, characterized by x-ray diffraction and microscopy, and used in batch sorption and column breakthrough experiments. Solutions with pH 6.8 and 8.8 were tested. Solutions were switched to radionuclide-free synthetic Grimsel groundwater after near-steady actinide/colloid breakthrough occurred in column experiments. We are currently evaluating actinide adsorption/desorption rates as a function of water chemistry (initial focus on pH), with future testing planned to evaluate the influence of carbonate concentrations, flow rates, and mineralogy in solutions and suspensions with bentonite colloids. (auth)

  2. Potential radiation dose from eating fish exposed to actinide contamination

    Energy Technology Data Exchange (ETDEWEB)

    Emery, R.M.; Klopfer, D.C.; Baker, D.A.; Soldat, J.K. (Battelle Pacific Northwest Labs., Richland, WA (USA))

    1981-04-01

    The purpose of this work is to establish a maximum potential for transporting actinides to man via fish consumption. The study took place in U-pond, a nuclear waste pond on the Hanford Site. It has concentrations of /sup 238/U, /sup 238/Pu, sup(239,240)Pu and /sup 241/Am that are approx. 3 orders of magnitude greater than background levels. Fish living in the pond contain higher actinide concentrations than those observed in fish from any other location. Experiments were performed in U-Pond to determine maximum quantities of actinides that could accumulate in fillets and whole bodies of two centrarchid fish species. Doses to hypothetical consumers were then estimated. Results indicate that highest concentrations occurring in bluegill or bass muscle after more than a year's exposure to the pond would not be sufficient to produce a significant radiation dose to a human consumer, even if he ate 0.5 kg (of the order of 1 lb) of these fillets every day for 70 yr. Natural predators (heron or coyote), having lifetime diets of whole fish from U-Pond, would receive less radiation dose from the ingested actinides than from natural background sources.

  3. Functionalized pyrazines as ligands for minor actinide extraction and catalysis

    NARCIS (Netherlands)

    Nikishkin, N.

    2013-01-01

    The research presented in this thesis concerns the design of ligands for a wide range of applications, from nuclear waste treatment to catalysis. The strategies employed to design actinide-selective extractants, for instance, comprise the fine tuning of the ligand electronic properties as well as

  4. Nuclear fuel cycle-oriented actinides separation in China

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Jing; He, Xihong; Wang, Jianchen [Tsinghua Univ., Beijing (China). Inst. of Nuclear and New Energy Technology

    2014-04-01

    In the last decades, the separation of actinides was widely and continuously studied in China. A few kinds of salt-free reductants to adjust Pu and Np valences have been investigated. N,N-dimethylhydroxylamine is a good reductant with high reduction rate constants for the co-reduction of Pu(IV) and Np(VI), and monomethylhydrazine is a simple compound for the individual reduction of Np(VI). Advanced PUREX based on Organic Reductants (APOR) was proposed. Trialkylphosphine oxide (TRPO) with a single functional group was found to possess strong affinity to tri-, tetra- and hexa-valent actinides. TRPO process has been first explored in China for actinides partitioning from high level waste and the good partitioning performance was demonstrated by the hot test. High extraction selectivity for trivalent actinides over lanthanides by dialkyldithiophosphinic acids was originally found in China. A separation process based on purified Cyanex 301 for the separation of Am from lanthanides was presented and successfully tested in a battery of miniature centrifugal contactors. (orig.)

  5. RAPID SEPARATION OF ACTINIDES AND RADIOSTRONTIUM IN VEGETATION SAMPLES

    Energy Technology Data Exchange (ETDEWEB)

    Maxwell, S.

    2010-06-01

    A new rapid method for the determination of actinides and radiostrontium in vegetation samples has been developed at the Savannah River Site Environmental Lab (Aiken, SC, USA) that can be used in emergency response situations or for routine analysis. The actinides in vegetation method utilizes a rapid sodium hydroxide fusion method, a lanthanum fluoride matrix removal step, and a streamlined column separation process with stacked TEVA, TRU and DGA Resin cartridges. Lanthanum was separated rapidly and effectively from Am and Cm on DGA Resin. Alpha emitters are prepared using rare earth microprecipitation for counting by alpha spectrometry. The purified {sup 90}Sr fractions are mounted directly on planchets and counted by gas flow proportional counting. The method showed high chemical recoveries and effective removal of interferences. The actinide and {sup 90}Sr in vegetation sample analysis can be performed in less than 8 h with excellent quality for emergency samples. The rapid fusion technique is a rugged sample digestion method that ensures that any refractory actinide particles or vegetation residue after furnace heating is effectively digested.

  6. Functionalized pyrazines as ligands for minor actinide extraction and catalysis

    NARCIS (Netherlands)

    Nikishkin, N.

    2013-01-01

    The research presented in this thesis concerns the design of ligands for a wide range of applications, from nuclear waste treatment to catalysis. The strategies employed to design actinide-selective extractants, for instance, comprise the fine tuning of the ligand electronic properties as well as us

  7. Preparation of actinide targets and sources using nonaqueous electrodeposition

    Energy Technology Data Exchange (ETDEWEB)

    Fowler, M.M.; Gursky, J.C.; Wilhelmy, J.B. (Los Alamos National Lab., NM (USA))

    1991-05-15

    Application of the method of 'molecular plating' to prepare actinide targets suitable for accelerator bombardment is presented. Two example applications involving {sup 229}Th and {sup 254}Es are discussed along with the merits and liabilities of the method. (orig.).

  8. Actinide biocolloid formation in brine by halophilic bacteria

    Energy Technology Data Exchange (ETDEWEB)

    Gillow, J.B.; Francis, A.J.; Dodge, C.J. [Brookhaven National Lab., Upton, NY (United States); Harris, R.; Beveridge, T.J. [Univ. of Guelph, Ontario (Canada); Brady, P.V.; Papenguth, H.W. [Sandia National Labs., Albuquerque, NM (United States)

    1998-12-31

    The authors examined the ability of a halophilic bacterium (WIPP 1A) isolated from the Waste Isolation Pilot Plant (WIPP) site to accumulate uranium in order to determine the potential for biocolloid facilitated actinide transport. The bacterial cell surface functional groups involved in the complexation of the actinide were determined by titration. Uranium, added as uranyl nitrate, was removed from solution at pH 5 by cells but at pH 7 and 9 very little uranium was removed due to its limited solubility. Although present as soluble species, uranyl citrate at pH 5, 7, and 9, and uranyl carbonate at pH 9 were not removed by the bacterium because they were not bioavailable due to their neutral or negative charge. Addition of uranyl EDTA to brine at pH 5, 7, and 9 resulted in the immediate precipitation of U. Transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDS) analysis revealed that uranium was not only associated with the cell surface but also accumulated intracellularly as uranium-enriched granules. Extended X-ray absorption fine structure (EXAFS) analysis of the bacterial cells indicated the bulk sample contained more than one uranium phase. Nevertheless these results show the potential for the formation of actinide bearing bacterial biocolloids that are strictly regulated by the speciation and bioavailability of the actinide.

  9. ACTINIDE BIOCOLLOID FORMATION IN BRINE BY HALOPHILIC BACTERIA

    Energy Technology Data Exchange (ETDEWEB)

    GILLOW,J.B.; FRANCIS,A.J.; DODGE,C.J.; HARRIS,R.; BEVERIDGE,T.J.; BRADY,P.B.; PAPENGUTH,H.W.

    1998-11-09

    The authors examined the ability of a halophilic bacterium (WIPP 1A) isolated from the Waste Isolation Pilot Plant (WIPP) site to accumulate uranium in order to determine the potential for biocolloid facilitated actinide transport. The bacterial cell surface functional groups involved in the complexation of the actinide were determined by titration. Uranium, added as uranyl nitrate, was removed from solution at pH 5 by cells but at pH 7 and 9 very little uranium was removed due to its limited solubility. Although present as soluble species, uranyl citrate at pH 5, 7, and 9, and uranyl carbonate at pH 9 were not removed by the bacterium because they were not bioavailable due to their neutral or negative charge. Addition of uranyl EDTA to brine at pH 5, 7, and 9 resulted in the immediate precipitation of U. Transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDS) analysis revealed that uranium was not only associated with the cell surface but also accumulated intracellularly as uranium-enriched granules. Extended X-ray absorption fine structure (EXAFS) analysis of the bacterial cells indicated the bulk sample contained more than one uranium phase. Nevertheless these results show the potential for the formation of actinide bearing bacterial biocolloids that are strictly regulated by the speciation and bioavailability of the actinide.

  10. Actinide Biocolloid Formation in Brine by Halophilic Bacteria

    Energy Technology Data Exchange (ETDEWEB)

    Gillow, J.B.; Francis, A.J.; Dodge, C.J.; Harris, R.; Beveridge, T.J.; Brady, P.V.; Papenguth, H.W.

    1999-07-28

    We examined the ability of a halophilic bacterium (WFP 1A) isolated from the Waste Isolation Pilot Plant (WIPP) site to accumulate uranium in order to determine the potential for biocolloid facilitated actinide transport. The bacterial cell Surface functional groups involved in the complexation of the actinide were determined by titration. Uranium, added as uranyl nitrate, was removed from solution at pH 5 by cells but at pH 7 and 9 very little uranium was removed due to its limited volubility. Although present as soluble species, uranyl citrate at pH 5, 7, and 9, and uranyl carbonate at pH 9 were not removed by the bacterium because they were not bioavailable due to their neutral or negative charge. Addition of uranyl EDTA to brine at pH 5, 7, and 9 resulted in the immediate precipitation of U. Transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDS) analysis revealed that uranium was not only associated with the cell surface but also accumulated intracellulary as uranium-enriched granules. Extended X-ray absorption fine structure (EXAFS) analysis, of the bacterial cells indicated the bulk sample contained more than one uranium phase. Nevertheless these results show the potential for the formation of actinide bearing bacterial biocolloids that are strictly regulated by the speciation and bioavailability of the actinide.

  11. Electron-phonon coupling of the actinide metals

    DEFF Research Database (Denmark)

    Skriver, H. L.; Mertig, I.

    1985-01-01

    -phonon parameter λ is found to attain its maximum value in Ac, and they predict a transition temperature of 9K for this metal. In the light actinides Th through Pu, λ is found to be of order 0.4 and within a factor of 2 of experiments which is also the accuracy found in studies of the transition metals...

  12. Actinides How well do we know their stellar production?

    CERN Document Server

    Goriely, S

    2001-01-01

    The reliable evaluation of the r-process production of the actinides and careful estimates of the uncertainties affecting these predictions are key ingredients especially in nucleo-cosmochronology studies based on the analysis of very metal-poor stars or on the composition of meteorites. This type of information is also required in order to make the best possible use of future high precision data on the actinide composition of galactic cosmic rays, of the local interstellar medium, or of meteoritic grains of presumed circumstellar origin. This paper provides the practitioners in these various fields with the most detailed and careful analysis of the r-process actinide production available to-date. In total, thirty-two different multi-event canonical calculations using different nuclear ingredients or astrophysics conditions are presented, and are considered to give a fair picture of the level of reliability of the predictions of the actinide production, at least in the framework of a simple r-process model. T...

  13. Spent Nuclear Fuel Option Study on Hybrid Reactor for Waste Transmutation

    Energy Technology Data Exchange (ETDEWEB)

    Hong, Seong Hee; Kim, Myung Hyun [Kyung Hee University, Yongin (Korea, Republic of)

    2016-05-15

    DUPIC nuclear fuel can be used in hybrid reactor by compensation of subcritical level through (U-10Zr) fuel. Energy production performance of Hyb-WT with DUPIC is grateful because it has high EM factor and performs waste transmutation at the same time. However, waste transmutation performance should be improved by different fissile fuel instead of (U-10Zr) fuel. SNF (Spent Nuclear Fuel) disposal is one of the problems in the nuclear industry. FFHR (Fusion-Fission Hybrid Reactor) is one of the most attractive option on reuse of SNF as a waste transmutation system. Because subcritical system like FFHR has some advantages compared to critical system. Subcritical systems have higher safety potential than critical system. Also, there is suppressed excess reactivity at BOC (Beginning of Cycle) in critical system, on the other hand there is no suppressed reactivity in subcritical system. Our research team could have designed FFHR for waste transmutation; Hyb-WT. Various researches have been conducted on fuel and coolant option for optimization of transmutation performance. However, Hyb-WT has technical disadvantage. It is required fusion power (Pfus) which is the key design parameter in FFHR is increased for compensation of decreasing subcritical level. As a result, structure material integrity is damaged under high irradiation condition by increasing Pfus. Also, deep burn of reprocessed SNF is limited by weakened integrity of structure material. Therefore, in this research, SNF option study will be conducted on DUPIC (Direct Use of Spent PWR Fuel in CANDU Reactor) fuel, TRU fuel and DUPIC + TRU mixed fuel for optimization of Hyb-WT performance. Goal of this research is design check for low required fusion power and high waste transmutation. In this paper, neutronic analysis is conducted on Hyb-WT with DUPIC nuclear fuel. When DUPIC nuclear fuel is loaded in fast neutron system, supplement fissile materials need to be loaded together for compensation of low criticality

  14. Sequestering agents for the removal of actinides from waste streams

    Energy Technology Data Exchange (ETDEWEB)

    Raymond, K.N.; White, D.J.; Xu, Jide; Mohs, T.R. [Univ. of California, Berkeley, CA (United States)

    1997-10-01

    The goal of this project is to take a biomimetic approach toward developing new separation technologies for the removal of radioactive elements from contaminated DOE sites. To achieve this objective, the authors are investigating the fundamental chemistry of naturally occurring, highly specific metal ion sequestering agents and developing them into liquid/liquid and solid supported actinide extraction agents. Nature produces sideophores (e.g., Enterobactin and Desferrioxamine B) to selectivity sequester Lewis acidic metal ions, in particular Fe(III), from its surroundings. These chelating agents typically use multiple catechols or hydroxamic acids to form polydentate ligands that chelate the metal ion forming very stable complexes. The authors are investigating and developing analogous molecules into selective chelators targeting actinide(IV) ions, which display similar properties to Fe(III). By taking advantage of differences in charge, preferred coordination number, and pH stability range, the transition from nature to actinide sequestering agents has been applied to the development of new and highly selective actinide extraction technologies. Additionally, the authors have shown that these chelating ligands are versatile ligands for chelating U(VI). In particular, they have been studying their coordination chemistry and fundamental interactions with the uranyl ion [UO{sub 2}]{sup 2+}, the dominant form of uranium found in aqueous media. With an understanding of this chemistry, and results obtained from in vivo uranium sequestration studies, it should be possible to apply these actinide(IV) extraction technologies to the development of new extraction agents for the removal of uranium from waste streams.

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

    Energy Technology Data Exchange (ETDEWEB)

    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.

  16. Application of neutron transmutation doping method to initially p-type silicon material.

    Science.gov (United States)

    Kim, Myong-Seop; Kang, Ki-Doo; Park, Sang-Jun

    2009-01-01

    The neutron transmutation doping (NTD) method was applied to the initially p-type silicon in order to extend the NTD applications at HANARO. The relationship between the irradiation neutron fluence and the final resistivity of the initially p-type silicon material was investigated. The proportional constant between the neutron fluence and the resistivity was determined to be 2.3473x10(19)nOmegacm(-1). The deviation of the final resistivity from the target for almost all the irradiation results of the initially p-type silicon ingots was at a range from -5% to 2%. In addition, the burn-up effect of the boron impurities, the residual (32)P activity and the effect of the compensation characteristics for the initially p-type silicon were studied. Conclusively, the practical methodology to perform the neutron transmutation doping of the initially p-type silicon ingot was established.

  17. Hydrogen bond disruption in DNA base pairs from (14)C transmutation.

    Science.gov (United States)

    Sassi, Michel; Carter, Damien J; Uberuaga, Blas P; Stanek, Christopher R; Mancera, Ricardo L; Marks, Nigel A

    2014-09-04

    Recent ab initio molecular dynamics simulations have shown that radioactive carbon does not normally fragment DNA bases when it decays. Motivated by this finding, density functional theory and Bader analysis have been used to quantify the effect of C → N transmutation on hydrogen bonding in DNA base pairs. We find that (14)C decay has the potential to significantly alter hydrogen bonds in a variety of ways including direct proton shuttling (thymine and cytosine), thermally activated proton shuttling (guanine), and hydrogen bond breaking (cytosine). Transmutation substantially modifies both the absolute and relative strengths of the hydrogen bonding pattern, and in two instances (adenine and cytosine), the density at the critical point indicates development of mild covalent character. Since hydrogen bonding is an important component of Watson-Crick pairing, these (14)C-induced modifications, while infrequent, may trigger errors in DNA transcription and replication.

  18. Separation of technetium from ruthenium after the accelerator transmutation of technetium

    Energy Technology Data Exchange (ETDEWEB)

    Abney, K.D.; Schroeder, N.C.; Kinkead, S.A.; Attrep, M. Jr.

    1992-01-01

    Both civilian and defense related waste must be processed with a strategy for dealing with Tc. One solution is to remove the Tc from the waste steam and transmute the Tc to stable Ru in either a reactor or an accelerator. Before any processing of waste streams can be performed (even if transmutation is not performed) the separations chemistry from the spent fuels or the stored wastes containing Tc must be developed. This report details some of the separation schemes possible for the separation of Tc and Ru, which include the baseline ion exchange process of Roberts, Smith and Wheelwright, ozonolysis, filtration, magnetic separation, solvent extraction, electrodeposition, fluorination, and pyrolysis. 5 figs, 4 refs. (DLC)

  19. General form of the Euler-Poisson-Darboux equation and application of the transmutation method

    Directory of Open Access Journals (Sweden)

    Elina L. Shishkina

    2017-07-01

    Full Text Available In this article, we find solution representations in the compact integral form to the Cauchy problem for a general form of the Euler-Poisson-Darboux equation with Bessel operators via generalized translation and spherical mean operators for all values of the parameter k, including also not studying before exceptional odd negative values. We use a Hankel transform method to prove results in a unified way. Under additional conditions we prove that a distributional solution is a classical one too. A transmutation property for connected generalized spherical mean is proved and importance of applying transmutation methods for differential equations with Bessel operators is emphasized. The paper also contains a short historical introduction on differential equations with Bessel operators and a rather detailed reference list of monographs and papers on mathematical theory and applications of this class of differential equations.

  20. Implications of transmutation on the defect chemistry in crystalline waste forms

    Energy Technology Data Exchange (ETDEWEB)

    Uberuaga, B.P., E-mail: blas@lanl.go [Materials Science and Technology Division, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Jiang, C.; Stanek, C.R.; Sickafus, K.E. [Materials Science and Technology Division, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Marks, N.A. [Nanochemistry Research Institute, Curtin University of Technology, P.O. Box U1987, Perth, WA 6845 (Australia); Carter, D.J.; Rohl, A.L. [Nanochemistry Research Institute, Curtin University of Technology, P.O. Box U1987, Perth, WA 6845 (Australia); iVEC, Technology Park, Kensington, WA 6151 (Australia)

    2010-10-01

    Radioactive decay within the solid state creates chemical environments which are typically incommensurate with the initial host structure. Using a combined theoretical and computational approach, we discuss this 'transmutation problem' in the context of the short-lived fission products Cs-137 and Sr-90. We show how a Kroeger-Vink treatment is insufficient for understanding defects arising from transmutation, and present density functional theory data for chemical evolution within two prototypical hosts, CsCl and SrTiO{sub 3}. While the latter has a strong driving force for phase separation with increasing Zr content, the Cs(Ba)Cl system is surprisingly stable. The sharp difference between these two findings points to the need for better understanding of novel chemistry in nuclear waste forms.

  1. System and safety studies of accelerator driven transmutation. Annual Report 2001

    Energy Technology Data Exchange (ETDEWEB)

    Gudowski, W.; Wallenius, J.; Tucek, K.; Eriksson, Marcus; Carlsson, Johan; Seltborg, P.; Cetnar, J.; Chakarova, R.; Westlen, D. [Royal Inst. of Tech., Stockholm (Sweden). Dept. of Nuclear and Reactor Physics

    2002-03-01

    The research on safety of Accelerator-Driven Transmutation Systems (ADS) at the Dept. of Nuclear and Reactor Physics has been focused in year 2001 on: a) ADS core design and development of advanced nuclear fuel optimised for high transmutation rates and good safety features; b) analysis of ADS-dynamics; c) computer code and nuclear data development relevant for simulation and optimization of ADS; d) participation in ADS experiments including 1 MW spallation target manufacturing, subcritical experiments MUSE (CEA-Cadarache) and YALINA experiment in Minsk. The Dept. is very actively participating in many European projects in the 5th Framework Programme of the European Community. Most of the research topics reported in this paper are referred to by appendices, which have been published in the open literature. The topics, which are not yet published, are described here in more details.

  2. Plutonium and Minor Actinide Management in Thermal High-Temperature Gas-Cooled Reactors. Publishable Final Activity Report

    Energy Technology Data Exchange (ETDEWEB)

    Kuijper, J.C., E-mail: kuijper@nrg.eu [Nuclear Research and Consultancy Group (NRG), Petten (Netherlands); Somers, J.; Van Den Durpel, L.; Chauvet, V.; Cerullo, N.; Cetnar, J.; Abram, T.; Bakker, K.; Bomboni, E.; Bernnat, W.; Domanska, J.G.; Girardi, E.; De Haas, J.B.M.; Hesketh, K.; Hiernaut, J.P.; Hossain, K.; Jonnet, J.; Kim, Y.; Kloosterman, J.L.; Kopec, M.; Murgatroyd, J.; Millington, D.; Lecarpentier, D.; Lomonaco, G.; McEachern, D.; Meier, A.; Mignanelli, M.; Nabielek, H.; Oppe, J.; Petrov, B.Y.; Pohl, C.; Ruetten, H.J.; Schihab, S.; Toury, G.; Trakas, C.; Venneri, F.; Verfondern, K.; Werner, H.; Wiss, T.; Zakova, J.

    2010-11-15

    The PUMA project -the acronym stands for 'Plutonium and Minor Actinide Management in Thermal High-Temperature Gas-Cooled Reactors'- was a Specific Targeted Research Project (STREP) within the EURATOM 6th Framework Program (EU FP6). The PUMA project ran from September 1, 2006, until August 31, 2009, and was executed by a consortium of 14 European partner organisations and one from the USA. This report serves 2 purposes. It is both the 'Publishable Final Activity Report' and the 'Final (Summary) Report', describing, per Work Package, the specific objectives, research activities, main conclusions, recommendations and supporting documents. PUMA's main objective was to investigate the possibilities for the utilisation and transmutation of plutonium and especially minor actinides in contemporary and future (high temperature) gas-cooled reactor designs, which are promising tools for improving the sustainability of the nuclear fuel cycle. This contributes to the reduction of Pu and MA stockpiles, and also to the development of safe and sustainable reactors for CO{sub 2}-free energy generation. The PUMA project has assessed the impact of the introduction of Pu/MA-burning HTRs at three levels: fuel and fuel performance (modelling), reactor (transmutation performance and safety) and reactor/fuel cycle facility park. Earlier projects already indicated favourable characteristics of HTRs with respect to Pu burning. So, core physics of Pu/MA fuel cycles for HTRs has been investigated to study the CP fuel and reactor characteristics and to assure nuclear stability of a Pu/MA HTR core, under both normal and abnormal operating conditions. The starting point of this investigation comprised the two main contemporary HTR designs, viz. the pebble-bed type HTR, represented by the South-African PBMR, and hexagonal block type HTR, represented by the GT-MHR. The results (once again) demonstrate the flexibility of the contemporary (and near future) HTR

  3. Application of gas-cooled Accelerator Driven System (ADS) transmutation devices to sustainable nuclear energy development

    OpenAIRE

    2011-01-01

    The conceptual design of a pebble bed gas-cooled transmutation device is shown with the aim to evaluate its potential for its deployment in the context of the sustainable nuclear energy development, which considers high temperature reactors for their operation in cogeneration mode, producing electricity, heat and Hydrogen. As differential characteristics our device operates in subcritical mode, driven by a neutron source activated by an accelerator that adds clear safety advantages and fuel f...

  4. Dimensional transmutation in the longitudinal sector of equivariantly gauge-fixed Yang-Mills theory

    CERN Document Server

    Golterman, Maarten

    2014-01-01

    We study the pure-gauge sector of an $SU(N)$ gauge theory, equivariantly gauge fixed to $SU(N-1)\\times U(1)$, which is an asymptotically free non-linear sigma model in four dimensions. We show that dimensional transmutation takes place in the large-$N$ limit, and elaborate on the relevance of this result for a speculative scenario in which the strong longitudinal dynamics gives rise to a novel Higgs-Coulomb phase.

  5. Neutron Transmutation Doped (NTD) germanium thermistors for sub-mm bolometer applications

    Science.gov (United States)

    Haller, E. E.; Itoh, K. M.; Beeman, J. W.

    1996-01-01

    Recent advances in the development of neutron transmutation doped (NTD) semiconductor thermistors fabricated from natural and controlled isotopic composition germanium are reported. The near ideal doping uniformity that can be achieved with the NTD process, the device simplicity of NTD Ge thermistors and the high performance of cooled junction field effect transistor preamplifiers led to the widespread acceptance of these thermal sensors in ground-based, airborne and spaceborne radio telescopes. These features made possible the development of efficient bolometer arrays.

  6. Internal contamination by actinides after wounding: a robust rodent model for assessment of local and distant actinide retention.

    Science.gov (United States)

    Griffiths, N M; Wilk, J C; Abram, M C; Renault, D; Chau, Q; Helfer, N; Guichet, C; Van der Meeren, A

    2012-08-01

    Internal contamination by actinides following wounding may occur in nuclear fuel industry workers or subsequent to terrorist activities, causing dissemination of radioactive elements. Contamination by alpha particle emitting actinides can result in pathological effects, either local or distant from the site of entry. The objective of the present study was to develop a robust experimental approach in the rat for short- and long- term actinide contamination following wounding by incision of the skin and muscles of the hind limb. Anesthetized rats were contaminated with Mixed OXide (MOX, uranium, plutonium oxides containing 7.1% plutonium) or plutonium nitrate (Pu nitrate) following wounding by deep incision of the hind leg. Actinide excretion and tissue levels were measured as well as histological changes from 2 h to 3 mo. Humid swabs were used for rapid evaluation of contamination levels and proved to be an initial guide for contamination levels. Although the activity transferred from wound to blood is higher after contamination with a moderately soluble form of plutonium (nitrate), at 7 d most of the MOX (98%) or Pu nitrate (87%) was retained at the wound site. Rapid actinide retention in liver and bone was observed within 24 h, which increased up to 3 mo. After MOX contamination, a more rapid initial urinary excretion of americium was observed compared with plutonium. At 3 mo, around 95% of activity remained at the wound site, and excretion of Pu and Am was extremely low. This experimental approach could be applied to other situations involving contamination following wounding including rupture of the dermal, vascular, and muscle barriers.

  7. Actinides: How well do we know their stellar production?

    Science.gov (United States)

    Goriely, S.; Arnould, M.

    2001-12-01

    The reliable evaluation of the r-process production of the actinides and careful estimates of the uncertainties affecting these predictions are key ingredients especially in nucleo-cosmochronology studies based on the analysis of very metal-poor stars or on the composition of meteorites. This type of information is also required in order to make the best possible use of future high precision data on the actinide composition of galactic cosmic rays, of the local interstellar medium, or of meteoritic grains of presumed circumstellar origin. This paper provides the practitioners in these various fields with the most detailed and careful analysis of the r-process actinide production available to-date. This study is based on a version of the multi-event canonical model of the r-process which discards the largely used waiting point approximation. It considers also different combinations of models for the calculation of nuclear masses, beta -decay and fission rates. Two variants of the model used to predict nuclear reaction rates are adopted. In addition, the influence of the level of Pb and Bi production by the r-process on the estimated actinide production is evaluated by relying on the solar abundances of these two elements. In total, thirty-two different cases are presented, and are considered to give a fair picture of the level of reliability of the predictions of the actinide production, at least in the framework of a simple r-process model. This simplicity is imposed by our inability to identify the proper astrophysical sites for the r-process. As a guide to the practitioners, constraints on the actinide yield predictions and associated uncertainties are suggested on grounds of the measured abundances of r-nuclides, including Th and U, in the star CS 31082-001, and under the critical and questionable assumption of the ``universality'' of the r-process. We also define alternative constraints based on the nucleo-cosmochronological results derived from the present

  8. Fermilab Project X nuclear energy application: Accelerator, spallation target and transmutation technology demonstration

    Energy Technology Data Exchange (ETDEWEB)

    Gohar, Yousry; /Argonne; Johnson, David; Johnson, Todd; Mishra, Shekhar; /Fermilab

    2011-04-01

    The recent paper 'Accelerator and Target Technology for Accelerator Driven Transmutation and Energy Production' and report 'Accelerators for America's Future' have endorsed the idea that the next generation particle accelerators would enable technological breakthrough needed for nuclear energy applications, including transmutation of waste. In the Fall of 2009 Fermilab sponsored a workshop on Application of High Intensity Proton Accelerators to explore in detail the use of the Superconducting Radio Frequency (SRF) accelerator technology for Nuclear Energy Applications. High intensity Continuous Wave (CW) beam from the Superconducting Radio Frequency (SRF) Linac (Project-X) at beam energy between 1-2 GeV will provide an unprecedented experimental and demonstration facility in the United States for much needed nuclear energy Research and Development. We propose to carry out an experimental program to demonstrate the reliability of the accelerator technology, Lead-Bismuth spallation target technology and a transmutation experiment of spent nuclear fuel. We also suggest that this facility could be used for other Nuclear Energy applications.

  9. Fluoride partitioning R and D programme for molten salt transmutation reactor systems in the Czech Republic

    Energy Technology Data Exchange (ETDEWEB)

    Uhlir, J. [Nuclear Research Institute Rez plc, CZ (Czech Republic); Priman, V.; Vanicek, J. [Czech Power Company, Praha (Czech Republic)

    2001-07-01

    The transmutation of spent nuclear fuel is considered a prospective alternative conception to the current conception based on the non-reprocessed spent fuel disposal into underground repository. The Czech research and development programme in the field of partitioning and transmutation is founded on the Molten Salt Transmutation Reactor system concept with fluoride salts based liquid fuel, the fuel cycle of which is grounded on pyrochemical / pyrometallurgical fluoride partitioning of spent fuel. The main research activities in the field of fluoride partitioning are oriented mainly towards technological research of Fluoride Volatility Method and laboratory research on electro-separation methods from fluoride melts media. The Czech national conception in the area of P and T research issues from the national power industry programme and from the Czech Power Company intentions of the extensive utilization of nuclear power in our country. The experimental R and D work is concentrated mainly in the Nuclear Research Institute Rez plc that plays a role of main nuclear research workplace for the Czech Power Company. (author)

  10. Conceptual Design of Low Fusion Power Hybrid System for Waste Transmutation

    Energy Technology Data Exchange (ETDEWEB)

    Hong, Seong Hee; Kim, Myung Hyun [Kyung Hee University, Yongin (Korea, Republic of)

    2016-10-15

    DRUP (Direct Reuse of Used PWR) fuel has same process with DUPIC (Direct Use of spent PWR fuel Into CANDU reactor). There are 2 big benefits by using DRUP fuel in Hybrid system. One is fissile production during operating period. Required power is decreased by fissile production from DRUP fuel. When the fusion power is reduced, integrity of structure materials is not significantly weakened due to reduction of 14.1MeV high energy neutrons. In addition, required amount of tritium for self-sufficiency TBR (Tritium Breeding Ratio ≥ 1.1) is decreased. Therefore, it is possible to further loading the SNF as much as the amount of lithium decreased. It is effective in transmutation. The other one is that DRUP fuel is also SNF. Therefore, using DRUP fuel is reusing of SNF, as a result it makes reduction of SNF from PWR. However, thermal neutron system is suitable for using DRUP fuel compared to fast neutron system. Therefore, transmutation zone designed (U-TRU)Zr fuel and fissile production zone designed DRUP fuel are separated in this study. In this paper, using DRUP fuel for low fusion power in hybrid system is suggested. Fusion power is decreased by using DRUP fuel. As a result, TBR is satisfied design condition despite of using natural lithium. In addition, not only (U-TRU)Zr fuel but also DRUP fuel are transmuted.

  11. Solubility of actinides and surrogates in nuclear glasses; Solubilite des actinides et de leurs simulants dans les verres nucleaires. Limites d'incorporation et comprehension des mecanismes

    Energy Technology Data Exchange (ETDEWEB)

    Lopez, Ch

    2003-07-01

    The nuclear wastes are currently incorporated in borosilicate glass matrices. The resulting glass must be perfectly homogeneous. The work discussed here is a study of actinide (thorium and plutonium) solubility in borosilicate glass, undertaken to assess the extent of actinide solubility in the glass and to understand the mechanisms controlling actinide solubilization. Glass specimens containing; actinide surrogates were used to prepare and optimize the fabrication of radioactive glass samples. These preliminary studies revealed that actinide Surrogates solubility in the glass was enhanced by controlling the processing temperature, the dissolution kinetic of the surrogate precursors, the glass composition and the oxidizing versus reducing conditions. The actinide solubility was investigated in the borosilicate glass. The evolution of thorium solubility in borosilicate glass was determined for temperatures ranging from 1200 deg C to 1400 deg C.Borosilicate glass specimens containing plutonium were fabricated. The experimental result showed that the plutonium solubility limit ranged from 1 to 2.5 wt% PuO{sub 2} at 1200 deg C. A structural approach based on the determination of the local structure around actinides and their surrogates by EXAFS spectroscopy was used to determine their structural role in the glass and the nature of their bonding with the vitreous network. This approach revealed a correlation between the length of these bonds and the solubility of the actinides and their surrogates. (author)

  12. Fabrication of targets for transmutation of americium : synthesis of inertial matrix by sol-gel method. Procedure study on the infiltration of a radioactive solutions; Fabricacion de blancos para la transmutacion de americio: sintesis de matrices inertes por el metodo sol-gel. Estudio del procedimiento de infiltracion de disoluciones radiactivas

    Energy Technology Data Exchange (ETDEWEB)

    Fernandez Carretero, A. [Universidad Complutense de Madrid (Spain)

    2002-07-01

    Transmutation and incineration are innovative options in the management and disposal of fission products and actinides. nevertheless, the fabrication of targets for transmutation and incineration of actinides and fission products require a reconsideration of conventional processes (mechanical blending) and the development of new procedures compatible with the high activity of these materials. This work presents th R and D of a new fabrication method called INRAM (Infiltration of Radioactive Materials) based on the infiltration of an actinide solution in a porous non radiotoxic material in the form of a pellet (up to 12% An), or beads (up to 40% An) produced by sol-gel. The first method have been used for the fabrication of spinel (MgAl{sub 2}O{sub 4}) targets containing 11% Am, which have been irradiated in HFR-Petten (358.4 full power days). Post-test burn-up calculations showed that at the end of the irradiation the initial Am-241 concentration was reduced to 4%. The fraction of the initial americum atoms that have been fissioned is 28%. The main advantage of the INRAM method is that matrices with low or zero activity can be fabricated and formed into the required shape in an unshielded facility. This method offers other advantages over conventional ones, such as the active wastes are reduced, is easy to automate, adoptable to telemanipulation and dust free, which facilitate operator intervention and minimise radiation exposure to the personal. In addition, the infiltrant needs only be present in liquid form, i. e. it could be transferred directly from the reprocessing plant for fabrication into targets without conversion into-solid form. In order to optimise the infiltration process in depth investigations of all important process parameters, e. g. infiltration kinetics and metal (pu, Am) concentration in the feed solution, and also on extensive study or powder metallurgy parameters for the preparation of high quality fuel pellets with a high density, have been

  13. Monazite-type ceramics for conditioning of minor actinides. Structural characterization and properties

    Energy Technology Data Exchange (ETDEWEB)

    Babelot, Carole

    2013-07-01

    The minor actinides (MA) neptunium, americium, and curium are mainly responsible for the long-term radiotoxicity of the High Active Waste (HAW) generated during the nuclear power operation. If these long-lived radionuclides are removed from the HAW by partitioning and converted by neutron fission (transmutation) into shorter-lived or stable elements, the remaining waste loses most of its long-term radiotoxicity. Thus, partitioning and transmutation (P and T) are considered as attractive options for reducing the burden on geological disposals. As an alternative, these separated MA can also be conditioned (P and C strategy) in specifically adapted ceramics to ensure their safe final disposal over long periods. At the moment, spent fuel elements are foreseen either for direct disposal in deep geological repositories or for reprocessing. The highly active liquid waste that is produced during reprocessing is conditioned industrially using a vitrification process before final disposal. Although the widely used borosilicate glasses meet most of the specifications needed, ceramic host matrices appear to be even more suitable in terms of resistance to corrosion. The development of new materials based on tailor-made highly specific ceramics with extremely stable behavior would make it possible to improve the final storage of long-lived high-level radiotoxic waste. In the framework of this PhD research project, monazite-type ceramics were chosen as promising host matrices for the conditioning of trivalent actinides. The focus on the monazite-type ceramics is justified by their properties such as high chemical durability. REPO{sub 4} ceramics are named monazite for RE = La - Gd (monoclinic symmetry) and xenotime for RE = Tb - Lu and Y (tetragonal symmetry). The objective of this study is to contribute to the understanding of the alteration behavior of such ceramics under the repository conditions. REPO{sub 4} (with RE = La, Eu) is prepared by hydrothermal synthesis at 200 C

  14. Monazite-type ceramics for conditioning of minor actinides. Structural characterization and properties

    Energy Technology Data Exchange (ETDEWEB)

    Babelot, Carole

    2013-07-01

    The minor actinides (MA) neptunium, americium, and curium are mainly responsible for the long-term radiotoxicity of the High Active Waste (HAW) generated during the nuclear power operation. If these long-lived radionuclides are removed from the HAW by partitioning and converted by neutron fission (transmutation) into shorter-lived or stable elements, the remaining waste loses most of its long-term radiotoxicity. Thus, partitioning and transmutation (P and T) are considered as attractive options for reducing the burden on geological disposals. As an alternative, these separated MA can also be conditioned (P and C strategy) in specifically adapted ceramics to ensure their safe final disposal over long periods. At the moment, spent fuel elements are foreseen either for direct disposal in deep geological repositories or for reprocessing. The highly active liquid waste that is produced during reprocessing is conditioned industrially using a vitrification process before final disposal. Although the widely used borosilicate glasses meet most of the specifications needed, ceramic host matrices appear to be even more suitable in terms of resistance to corrosion. The development of new materials based on tailor-made highly specific ceramics with extremely stable behavior would make it possible to improve the final storage of long-lived high-level radiotoxic waste. In the framework of this PhD research project, monazite-type ceramics were chosen as promising host matrices for the conditioning of trivalent actinides. The focus on the monazite-type ceramics is justified by their properties such as high chemical durability. REPO{sub 4} ceramics are named monazite for RE = La - Gd (monoclinic symmetry) and xenotime for RE = Tb - Lu and Y (tetragonal symmetry). The objective of this study is to contribute to the understanding of the alteration behavior of such ceramics under the repository conditions. REPO{sub 4} (with RE = La, Eu) is prepared by hydrothermal synthesis at 200 C

  15. Theory of the crystal structures of the actinide metals; Theorie des structures cristallines des metaux actinides

    Energy Technology Data Exchange (ETDEWEB)

    Penicaud, M. [CEA Bruyeres-le-Chatel, 91 (France)

    2005-07-01

    We describe, by bands calculation methods, the delocalized-localized transition of 5f electrons in the series of actinide metals, at ambient conditions, which happens between {alpha}-Pu and Am, and which is characterized by the change from the open and complex monoclinic crystal structure to the double hexagonal close-packed structure, and by the density collapse from 19.86 g.cm{sup -3} to 13.67 g.cm{sup -3}. The case of the alloy stabilized Pu in the high temperature {delta} phase (face centered cubic) is treated. Its ambient experimental density (15.92 g.cm{sup -3}) is obtained with a localization of the only 5f5/2 electrons. We find a 5f5/2 density of states peak pinned at the Fermi level, in agreement with photoelectron spectroscopy, and the high value of the electronic specific heat coefficient. The crystalline stability under pressure of U, Np, Pu and Am is examined. We find theoretically, at high pressure in Am, the stability of the recently discovered experimentally Am IV structure which is primitive-orthorhombic with four atoms in the unit cell. We calculate this structure also stable for Pu, for which it is proposed that the sequence is: {alpha}-Pu {yields} Am IV {yields} body-centered cubic. (author)

  16. The TMSR as actinide burner and thorium breeder

    Energy Technology Data Exchange (ETDEWEB)

    Merle-Lucotte, E.; Heuer, D.; Le Brun, C.; Allibert, M.; Ghetta, V. [LPSC/IN2P3/CNRS - INPG/ENSPG - UJF, 53, avenue des Martyrs, F-38026 Grenoble Cedex (France)

    2007-07-01

    Molten Salt Reactors (MSRs) are one of the six systems retained by Generation IV as a candidate for the next generation of nuclear reactors. Molten Salt Reactor is a very attractive concept especially for the Thorium fuel cycle which allows nuclear energy production with a very low production of radio-toxic minor actinides. Studies have thus been done on the Molten Salt Breeder Reactor (MSBR) of Oak-Ridge to re-evaluate this concept. They have shown that the MSBR suffers from major drawbacks concerning for example safety and reprocessing, drawbacks incompatible with any industrial development. On the other hand, the advantages of the Thorium fuel cycle were too attractive not to look further into it. With these considerations, we have reassessed the whole concept to propose an innovative reactor called Thorium Molten Salt Reactor (TMSR). Many parametric studies of the TMSR have been carried out, correlating the core arrangement and composition, the reprocessing performances, and the salt composition. In particular, by changing the moderation ratio of the core the neutron spectrum can be modified and placed anywhere between a very thermalized neutron spectrum and a relatively fast spectrum. Even if the epithermal TMSR configurations have not been completely excluded by our calculations, our studies have shown that the reactor design where there is no graphite moderator inside the core appears to be the most promising in terms of safety coefficients, reprocessing requirements, and breeding and deployment capabilities. Larger fissile matter inventories are necessary in such a reactor configuration compared to the thermalized TMSR configurations, but the resulting deployment limitation could be solved by using transuranic elements as initial fissile load. This work is based on the coupling of a neutron transport code called MCNP with the materials evolution code REM. The former calculates the neutron flux and the reaction rates in all the cells while the latter solves

  17. On the use of a molten salt fast reactor to apply an idealized transmutation scenario for the nuclear phase out.

    Science.gov (United States)

    Merk, Bruno; Rohde, Ulrich; Glivici-Cotruţă, Varvara; Litskevich, Dzianis; Scholl, Susanne

    2014-01-01

    In the view of transmutation of transuranium (TRU) elements, molten salt fast reactors (MSFRs) offer certain advantages compared to solid fuelled reactor types like sodium cooled fast reactors (SFRs). In the first part these advantages are discussed in comparison with the SFR technology, and the research challenges are analyzed. In the second part cycle studies for the MSFR are given for different configurations--a core with U-238 fertile, a fertile free core, and a core with Th-232 as fertile material. For all cases, the transmutation potential is determined and efficient transmutation performance for the case with thorium as a fertile material as well as for the fertile free case is demonstrated and the individual advantages are discussed. The time evolution of different important isotopes is analyzed. In the third part a strategy for the optimization of the transmutation efficiency is developed. The final aim is dictated by the phase out decision of the German government, which requests to put the focus on the determination of the maximal transmutation efficiency and on an as much as possible reduced leftover of transuranium elements at the end of the reactor life. This minimal leftover is achieved by a two step procedure of a first transmuter operation phase followed by a second deep burning phase. There the U-233, which is bred in the blanket of the core consisting of thorium containing salt, is used as feed. It is demonstrated, that transmutation rates up to more than 90% can be achieved for all transuranium isotopes, while the production of undesired high elements like californium is very limited. Additionally, the adaptations needed for the simulation of a MSFR, and the used tool HELIOS 1.10 is described.

  18. Importance of All-in-one (MCNPX2.7.0+CINDER2008) Code for Rigorous Transmutation Study

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Oyeon [Institute for Modeling and Simulation Convergence, Daegu (Korea, Republic of); Kim, Kwanghyun [RadTek Co. Ltd., Daejeon (Korea, Republic of)

    2015-10-15

    It can be utilized as a possible mechanism for reducing the volume and hazard of radioactive waste by transforming hazardous radioactive elements with long half-life into less hazardous elements with short halflife. Thus, the understanding of the transmutation mechanism and beneficial machinery design technologies are important and useful. Although the terminology transmutation was rooted back to alchemy which transforms the base metals into gold in the middle ages, Rutherford and Soddy were the first observers by discovering the natural transmutation as a part of radioactive decay of the alpha decay type in early 20th century. Along with the development of computing technology, analysis software, for example, CINDER was developed for rigorous atomic transmutation study. The code has a long history of development from the original work of T. England at Bettis Atomic Power Laboratory (BAPL) in the early 1960s. It has been used to calculate the inventory of nuclides in an irradiated material. CINDER'90 which is recently released involved an upgrade of the code to allow the spontaneous tracking of chains based upon the significant density or pass-by of a nuclide, where pass-by represents the density of a nuclide transforming to other nuclides. Nuclear transmutation process is governed by highly non-linear differential equation. Chaotic nature of the non-linear equation bespeaks the importance of the accurate input data (i.e. number of significant digits). Thus, reducing the human interrogation is very important for the rigorous transmutation study and 'allin- one' code structure is desired. Note that non-linear characteristic of the transmutation equation caused by the flux changes due to the number density change during a given time interval (intrinsic physical phenomena) is not considered in this study. In this study, we only emphasized the effects of human interrogation in the computing process solving nonlinear differential equations, as shown in

  19. On the Use of a Molten Salt Fast Reactor to Apply an Idealized Transmutation Scenario for the Nuclear Phase Out

    Science.gov (United States)

    Merk, Bruno; Rohde, Ulrich; Glivici-Cotruţă, Varvara; Litskevich, Dzianis; Scholl, Susanne

    2014-01-01

    In the view of transmutation of transuranium (TRU) elements, molten salt fast reactors (MSFRs) offer certain advantages compared to solid fuelled reactor types like sodium cooled fast reactors (SFRs). In the first part these advantages are discussed in comparison with the SFR technology, and the research challenges are analyzed. In the second part cycle studies for the MSFR are given for different configurations – a core with U-238 fertile, a fertile free core, and a core with Th-232 as fertile material. For all cases, the transmutation potential is determined and efficient transmutation performance for the case with thorium as a fertile material as well as for the fertile free case is demonstrated and the individual advantages are discussed. The time evolution of different important isotopes is analyzed. In the third part a strategy for the optimization of the transmutation efficiency is developed. The final aim is dictated by the phase out decision of the German government, which requests to put the focus on the determination of the maximal transmutation efficiency and on an as much as possible reduced leftover of transuranium elements at the end of the reactor life. This minimal leftover is achieved by a two step procedure of a first transmuter operation phase followed by a second deep burning phase. There the U-233, which is bred in the blanket of the core consisting of thorium containing salt, is used as feed. It is demonstrated, that transmutation rates up to more than 90% can be achieved for all transuranium isotopes, while the production of undesired high elements like californium is very limited. Additionally, the adaptations needed for the simulation of a MSFR, and the used tool HELIOS 1.10 is described. PMID:24690768

  20. On the use of a molten salt fast reactor to apply an idealized transmutation scenario for the nuclear phase out.

    Directory of Open Access Journals (Sweden)

    Bruno Merk

    Full Text Available In the view of transmutation of transuranium (TRU elements, molten salt fast reactors (MSFRs offer certain advantages compared to solid fuelled reactor types like sodium cooled fast reactors (SFRs. In the first part these advantages are discussed in comparison with the SFR technology, and the research challenges are analyzed. In the second part cycle studies for the MSFR are given for different configurations--a core with U-238 fertile, a fertile free core, and a core with Th-232 as fertile material. For all cases, the transmutation potential is determined and efficient transmutation performance for the case with thorium as a fertile material as well as for the fertile free case is demonstrated and the individual advantages are discussed. The time evolution of different important isotopes is analyzed. In the third part a strategy for the optimization of the transmutation efficiency is developed. The final aim is dictated by the phase out decision of the German government, which requests to put the focus on the determination of the maximal transmutation efficiency and on an as much as possible reduced leftover of transuranium elements at the end of the reactor life. This minimal leftover is achieved by a two step procedure of a first transmuter operation phase followed by a second deep burning phase. There the U-233, which is bred in the blanket of the core consisting of thorium containing salt, is used as feed. It is demonstrated, that transmutation rates up to more than 90% can be achieved for all transuranium isotopes, while the production of undesired high elements like californium is very limited. Additionally, the adaptations needed for the simulation of a MSFR, and the used tool HELIOS 1.10 is described.

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

    Science.gov (United States)

    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.

  2. Radioanalytical determination of actinides and fission products in Belarus soils.

    Science.gov (United States)

    Michel, H; Gasparro, J; Barci-Funel, G; Dalmasso, J; Ardisson, G; Sharovarov, G

    1999-04-01

    Alpha emitting actinides such as plutonium, americium or curium were measured by alpha-spectrometry after radiochemical separation. The short range of alpha-particles within matter requires, after a pre-concentration process, a succession of isolation and purification steps based on the valence states modification of the researched elements. For counting, actinides were electrodeposited in view to obtain the mass-less source necessary to avoid self-absorption of the emitted radiations. Activity concentrations of gamma-emitting fission products were calculated after measurement with high purity germanium detectors (HPGe). These different methods were used to analyse soils sampled in the Republic of Belarus, not far from the Chernobyl nuclear plant.

  3. Actinide-specific sequestering agents and decontamination applications

    Energy Technology Data Exchange (ETDEWEB)

    Smith, William L. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Materials and Molecular Research Division; Univ. of California, Berkeley, CA (United States). Dept. of Chemistry; Raymond, Kenneth N. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States). Materials and Molecular Research Division; Univ. of California, Berkeley, CA (United States). Dept. of Chemistry

    1981-04-07

    With the commercial development of nuclear reactors, the actinides have become very important industrial elements. A major concern of the nuclear industry is the biological hazard associated with nuclear fuels and their wastes. The acute chemical toxicity of tetravalent actinides, as exemplified by Th(IV), is similar to Cr(III) or Al(III). However, the acute toxicity of 239Pu(IV) is similar to strychnine, which is much more toxic than any of the non-radioactive metals such as mercury. Although the more radioactive isotopes of the transuranium elements are more acutely toxic by weight than plutonium, the acute toxicities of 239Pu, 241Am, and 244Cm are nearly identical in radiation dose, ~100 μCi/kg in rodents. Finally and thus, the extreme acute toxicity of 239Pu is attributed to its high specific activity of alpha emission.

  4. Comparative Study of f-Element Electronic Structure across a Series of Multimetallic Actinide, Lanthanide-Actinide and Lanthanum-Actinide Complexes Possessing Redox-Active Bridging Ligands

    Energy Technology Data Exchange (ETDEWEB)

    Schelter, Eric J.; Wu, Ruilian; Veauthier, Jacqueline M.; Bauer, Eric D.; Booth, Corwin H.; Thomson, Robert K.; Graves, Christopher R.; John, Kevin D.; Scott, Brian L.; Thompson, Joe D.; Morris, David E.; Kiplinger, Jaqueline L.

    2010-02-24

    A comparative examination of the electronic interactions across a series of trimetallic actinide and mixed lanthanide-actinide and lanthanum-actinide complexes is presented. Using reduced, radical terpyridyl ligands as conduits in a bridging framework to promote intramolecular metal-metal communication, studies containing structural, electrochemical, and X-ray absorption spectroscopy are presented for (C{sub 5}Me{sub 5}){sub 2}An[-N=C(Bn)(tpy-M{l_brace}C{sub 5}Me4R{r_brace}{sub 2})]{sub 2} (where An = Th{sup IV}, U{sup IV}; Bn = CH{sub 2}C{sub 6}H{sub 5}; M = La{sup III}, Sm{sup III}, Yb{sup III}, U{sup III}; R = H, Me, Et) to reveal effects dependent on the identities of the metal ions and R-groups. The electrochemical results show differences in redox energetics at the peripheral 'M' site between complexes and significant wave splitting of the metal- and ligand-based processes indicating substantial electronic interactions between multiple redox sites across the actinide-containing bridge. Most striking is the appearance of strong electronic coupling for the trimetallic Yb{sup III}-U{sup IV}-Yb{sup III}, Sm{sup III}-U{sup IV}-Sm{sup III}, and La{sup III}-U{sup IV}-La{sup III} complexes, [8]{sup -}, [9b]{sup -} and [10b]{sup -}, respectively, whose calculated comproportionation constant K{sub c} is slightly larger than that reported for the benchmark Creutz-Taube ion. X-ray absorption studies for monometallic metallocene complexes of U{sup III}, U{sup IV}, and U{sup V} reveal small but detectable energy differences in the 'white-line' feature of the uranium L{sub III}-edges consistent with these variations in nominal oxidation state. The sum of this data provides evidence of 5f/6d-orbital participation in bonding and electronic delocalization in these multimetallic f-element complexes. An improved, high-yielding synthesis of 4{prime}-cyano-2,2{prime}:6{prime},2{double_prime}-terpyridine is also reported.

  5. Future nuclear fuel cycles: Prospect and challenges for actinide recycling

    Science.gov (United States)

    Warin, Dominique

    2010-03-01

    The global energy context pleads in favour of a sustainable development of nuclear energy since the demand for energy will likely increase, whereas resources will tend to get scarcer and the prospect of global warming will drive down the consumption of fossil fuel. In this context, nuclear power has the worldwide potential to curtail the dependence on fossil fuels and thereby to reduce the amount of greenhouse gas emissions while promoting energy independence. How we deal with nuclear radioactive waste is crucial in this context. In France, the public's concern regarding the long-term waste management made the French Governments to prepare and pass the 1991 and 2006 Acts, requesting in particular the study of applicable solutions for still minimizing the quantity and the hazardousness of final waste. This necessitates High Active Long Life element (such as the Minor Actinides MA) recycling, since the results of fuel cycle R&D could significantly change the challenges for the storage of nuclear waste. HALL recycling can reduce the heat load and the half-life of most of the waste to be buried to a couple of hundred years, overcoming the concerns of the public related to the long-life of the waste and thus aiding the "burying approach" in securing a "broadly agreed political consensus" of waste disposal in a geological repository. This paper presents an overview of the recent R and D results obtained at the CEA Atalante facility on innovative actinide partitioning hydrometallurgical processes. For americium and curium partitioning, these results concern improvements and possible simplifications of the Diamex-Sanex process, whose technical feasibility was already demonstrated in 2005. Results on the first tests of the Ganex process (grouped actinide separation for homogeneous recycling) are also discussed. In the coming years, next steps will involve both better in-depth understanding of the basis of these actinide partitioning processes and, for the new promising

  6. Chemical and Ceramic Methods Toward Safe Storage of Actinides

    Energy Technology Data Exchange (ETDEWEB)

    P.E.D. Morgan; R.M. Housley; J.B. Davis; M.L. DeHaan

    2005-08-19

    A very import, extremely-long-term, use for monazite as a radwaste encapsulant has been proposed. THe use of ceramic La-monazite for sequestering actinides (isolating them from the environment), especially plutonium and some other radioactive elements )e.g., fission-product rare earths), had been especially championed by Lynn Boatner of ORNL. Monazite may be used alone or, copying its compatibility with many other minerals in nature, may be used in diverse composite combinations.

  7. EXAFS studies of actinide ions in aqueous solution

    Energy Technology Data Exchange (ETDEWEB)

    Karim, D P; Georgopoulos, P; Knapp, G S

    1979-01-01

    The applicability of the EXAFS technique in the study of actinide systems is discussed. Uranium L/sub III/-edge spectra obtained on an in-lab rotating anode EXAFS facility are presented and analyzed for crystalline UO/sub 2/F/sub 2/ and aqueous solutions containing hexavalent uranium ions. Methods for the extension of the technique to more dilute systems are discussed.

  8. Chemical properties of the heavier actinides and transactinides

    Energy Technology Data Exchange (ETDEWEB)

    Hulet, E.K.

    1981-01-01

    The chemical properties of each of the elements 99 (Es) through 105 are reviewed and their properties correlated with the electronic structure expected for 5f and 6d elements. A major feature of the heavier actinides, which differentiates them from the comparable lanthanides, is the increasing stability of the divalent oxidation state with increasing atomic number. The divalent oxidation state first becomes observable in the anhydrous halides of californium and increases in stability through the series to nobelium, where this valency becomes predominant in aqueous solution. In comparison with the analogous 4f electrons, the 5f electrons in the latter part of the series are more tightly bound. Thus, there is a lowering of the 5f energy levels with respect to the Fermi level as the atomic number increases. The metallic state of the heavier actinides has not been investigated except from the viewpoint of the relative volatility among members of the series. In aqueous solutions, ions of these elements behave as a normal trivalent actinides and lanthanides (except for nobelium). Their ionic radii decrease with increasing nuclear charge which is moderated because of increased screening of the outer 6p electrons by the 5f electrons. The actinide series of elements is completed with the element lawrencium (Lr) in which the electronic configuration is 5f/sup 14/7s/sup 2/7p. From Mendeleev's periodicity and Dirac-Fock calculations, the next group of elements is expected to be a d-transition series corresponding to the elements Hf through Hg. The chemical properties of elements 104 and 105 only have been studied and they indeed appear to show the properties expected of eka-Hf and eka-Ta. However, their nuclear lifetimes are so short and so few atoms can be produced that a rich variety of chemical information is probably unobtainable.

  9. Ground-state electronic structure of actinide monocarbides and mononitrides

    DEFF Research Database (Denmark)

    Petit, Leon; Svane, Axel; Szotek, Z.

    2009-01-01

    The self-interaction corrected local spin-density approximation is used to investigate the ground-state valency configuration of the actinide ions in the actinide monocarbides, AC (A=U,Np,Pu,Am,Cm), and the actinide mononitrides, AN. The electronic structure is characterized by a gradually...... increasing degree of f electron localization from U to Cm, with the tendency toward localization being slightly stronger in the (more ionic) nitrides compared to the (more covalent) carbides. The itinerant band picture is found to be adequate for UC and acceptable for UN, while a more complex manifold...... of competing localized and delocalized f-electron configurations underlies the ground states of NpC, PuC, AmC, NpN, and PuN. The fully localized 5f-electron configuration is realized in CmC (f7), CmN (f7), and AmN (f6). The observed sudden increase in lattice parameter from PuN to AmN is found to be related...

  10. A literature review of actinide-carbonate mineral interactions

    Energy Technology Data Exchange (ETDEWEB)

    Stout, D.L. [Missouri Univ., Columbia, MO (United States). Dept. of Geological Sciences; Carroll, S.A. [Lawrence Livermore National Lab., CA (United States)

    1993-10-01

    Chemical retardation of actinides in groundwater systems is a potentially important mechanism for assessing the performance of the Waste Isolation Pilot Plant (WIPP), a facility intended to demonstrate safe disposal of transuranic waste. Rigorous estimation of chemical retardation during transport through the Culebra Dolomite, a water-bearing unit overlying the WIPP, requires a mechanistic understanding of chemical reactions between dissolved elements and mineral surfaces. This report represents a first step toward this goal by examining the literature for pertinent experimental studies of actinide-carbonate interactions. A summary of existing models is given, along with the types of experiments on which these models are based. Articles pertaining to research into actinide interactions with carbonate minerals are summarized. Select articles involving trace element-carbonate mineral interactions are also reviewed and may serve as templates for future research. A bibliography of related articles is included. Americium(III), and its nonradioactive analog neodymium(III), partition strongly from aqueous solutions into carbonate minerals. Recent thermodynamic, kinetic, and surface studies show that Nd is preferentially removed from solution, forming a Nd-Ca carbonate solid solution. Neptunium(V) is rapidly removed from solution by carbonates. Plutonium incorporation into carbonates is complicated by multiple oxidation states. Little research has been done on the radium(H) and thorium(IV) carbonate systems. Removal of uranyl ion from solution by calcite is limited to monolayer surface coverage.

  11. Behavior of actinides in the Integral Fast Reactor fuel cycle

    Energy Technology Data Exchange (ETDEWEB)

    Courtney, J.C. [Louisiana State Univ., Baton Rouge, LA (United States). Nuclear Science Center; Lineberry, M.J. [Argonne National Lab., Idaho Falls, ID (United States). Technology Development Div.

    1994-06-01

    The Integral Fast Reactor (IFR) under development by Argonne National Laboratory uses metallic fuels instead of ceramics. This allows electrorefining of spent fuels and presents opportunities for recycling minor actinide elements. Four minor actinides ({sup 237}Np, {sup 240}Pu, {sup 241}Am, and {sup 243}Am) determine the waste storage requirements of spent fuel from all types of fission reactors. These nuclides behave the same as uranium and other plutonium isotopes in electrorefining, so they can be recycled back to the reactor without elaborate chemical processing. An experiment has been designed to demonstrate the effectiveness of the high-energy neutron spectra of the IFR in consuming these four nuclides and plutonium. Eighteen sets of seven actinide and five light metal targets have been selected for ten day exposure in the Experimental Breeder Reactor-2 which serves as a prototype of the IFR. Post-irradiation analyses of the exposed targets by gamma, alpha, and mass spectroscopy are used to determine nuclear reaction-rates and neutron spectra. These experimental data increase the authors` confidence in their ability to predict reaction rates in candidate IFR designs using a variety of neutron transport and diffusion programs.

  12. Behavior of actinides in the Integral Fast Reactor fuel cycle

    Energy Technology Data Exchange (ETDEWEB)

    Courtney, J.C. [Louisiana State Univ., Baton Rouge, LA (United States). Nuclear Science Center; Lineberry, M.J. [Argonne National Lab., Idaho Falls, ID (United States). Technology Development Div.

    1994-06-01

    The Integral Fast Reactor (IFR) under development by Argonne National Laboratory uses metallic fuels instead of ceramics. This allows electrorefining of spent fuels and presents opportunities for recycling minor actinide elements. Four minor actinides ({sup 237}Np, {sup 240}Pu, {sup 241}Am, and {sup 243}Am) determine the waste storage requirements of spent fuel from all types of fission reactors. These nuclides behave the same as uranium and other plutonium isotopes in electrorefining, so they can be recycled back to the reactor without elaborate chemical processing. An experiment has been designed to demonstrate the effectiveness of the high-energy neutron spectra of the IFR in consuming these four nuclides and plutonium. Eighteen sets of seven actinide and five light metal targets have been selected for ten day exposure in the Experimental Breeder Reactor-2 which serves as a prototype of the IFR. Post-irradiation analyses of the exposed targets by gamma, alpha, and mass spectroscopy are used to determine nuclear reaction-rates and neutron spectra. These experimental data increase the authors` confidence in their ability to predict reaction rates in candidate IFR designs using a variety of neutron transport and diffusion programs.

  13. Rapid separation method for actinides in emergency air filter samples.

    Science.gov (United States)

    Maxwell, Sherrod L; Culligan, Brian K; Noyes, Gary W

    2010-12-01

    A new rapid method for the determination of actinides and strontium in air filter samples has been developed at the Savannah River Site Environmental Lab (Aiken, SC, USA) that can be used in emergency response situations. The actinides and strontium in air filter method utilizes a rapid acid digestion method and a streamlined column separation process with stacked TEVA, TRU and Sr Resin cartridges. Vacuum box technology and rapid flow rates are used to reduce analytical time. Alpha emitters are prepared using cerium fluoride microprecipitation for counting by alpha spectrometry. The purified (90)Sr fractions are mounted directly on planchets and counted by gas flow proportional counting. The method showed high chemical recoveries and effective removal of interferences. This new procedure was applied to emergency air filter samples received in the NRIP Emergency Response exercise administered by the National Institute for Standards and Technology (NIST) in April, 2009. The actinide and (90)Sr in air filter results were reported in less than 4 h with excellent quality. Copyright 2010 Elsevier Ltd. All rights reserved.

  14. Crystalline matrices for the immobilization of plutonium and actinides

    Energy Technology Data Exchange (ETDEWEB)

    Anderson, E.B.; Burakov, E.E.; Galkin, Ya.B.; Starchenko, V.A.; Vasiliev, V.G. [V.G. Khlopin Radium Institute, St. Petersburg (Russian Federation)

    1996-05-01

    The management of weapon plutonium, disengaged as a result of conversion, is considered together with the problem of the actinide fraction of long-lived high level radioactive wastes. It is proposed to use polymineral ceramics based on crystalline host-phases: zircon ZrSiO{sub 4} and zirconium dioxide ZrO{sub 2}, for various variants of the management of plutonium and actinides (including the purposes of long-term safe storage or final disposal from the human activity sphere). It is shown that plutonium and actinides are able to form with these phases on ZrSiO{sub 4} and ZrO{sub 2} was done on laboratory level by the hot pressing method, using the plasmochemical calcination technology. To incorporate simulators of plutonium into the structure of ZrSiO{sub 4} and ZrO{sub 2} in the course of synthesis, an original method developed by the authors as a result of studying the high-uranium zircon (Zr,U) SiO{sub 4} form Chernobyl {open_quotes}lavas{close_quotes} was used.

  15. High resolution X-ray emission spectroscopy: An advanced tool for actinide research

    Energy Technology Data Exchange (ETDEWEB)

    Vitova, T; Brendebach, B; Dardenne, K; Denecke, M A; Lebid, A; Loeble, M; Rothe, J; Batuk, O N; Geckeis, H [Karlsruhe Institut fuer Technologie (KIT), Institut fuer Nukleare Entsorgung (INE), PO Box 3640, D-76021 Karlsruhe (Germany); Hormes, J; Liu, D [Physikalisches Institut, Nussallee 12, D-53115 Bonn (Germany); Breher, F, E-mail: tonya.vitova@kit.edu [Karlsruhe Institut fuer Technologie (KIT), Institut fuer Anorganische Chemie, Engesserstr. 15, D-76131 Karlsruhe (Germany)

    2010-03-15

    High resolution X-ray emission spectroscopy (HRXES) is becoming increasingly important for our understanding of electronic and coordination structures. The combination of such information with development of quantum theoretical tools will advance our capability for predicting reactivity and physical behavior especially of 5f elements. HRXES can be used to remove lifetime broadening by registering the partial fluorescence yield emitted by the sample (i.e., recording a windowed signal from the energy dispersed fluorescence emission while varying incident photon energy), thereby yielding highly resolved X-ray absorption fine structure (XAFS) spectra. Such spectra often display resonant features not observed in conventional XAFS. The spectrometer set-up can also be used for a wide range of other experiments, for example, resonant inelastic X-ray scattering (RIXS), where bulk electron configuration information in solids, liquids and gases is obtained. Valence-selective XAFS studies, where the local structure of a selected element's valence state present in a mixture of valence states can be obtained, as well as site-selective XAFS studies, where the coordination structure of a metal bound to selected elements can be differentiated from that of all the other ligating atoms. A HRXES spectrometer has been constructed and is presently being commissioned for use at the INE-Beamline for actinide research at the synchrotron source ANKA at FZK. We present the spectrometer's compact, modular design, optimized for attaining a wide range of energies, and first test measurement results. Examples from HRXES studies of lanthanides, actinides counter parts, are also shown.

  16. Actinides and lanthanides under pressure: the pseudopotential approach; Actinides et terres rares sous pression: approche pseudopotentiel

    Energy Technology Data Exchange (ETDEWEB)

    Richard, N

    2002-07-01

    In the Density Functional Theory Framework, the pseudopotential formalism offers a broader scope of study than other theoretical methods such as global relaxation of the parameters of the cell or ab initio molecular dynamics simulations. This method has been widely used to study light elements or transition metals but never to study f elements. We have generated two non local norm conserving Trouillier-Martins pseudopotentials (one in LDA and one in GGA) for the cerium. To check the validity of the pseudopotentials, we have calculated the equilibrium volume and the incompressibility modulus and compared our results to previous all-electron calculations. If the GGA and non linear core corrections are used, the equation of state is in a good agreement with the experimental equation of state. A static study of the previously proposed high pressure phases give a transitions fcc-a''(I)-bct. Using the pseudopotentials we have generated, an ab initio molecular dynamics simulation at constant pressure, in the region between 5 and 12 GPa where the stable phase of cerium is not well defined, lead us to predict that a centred monoclinic structure, as the a''(I) phase previously observed in some experiments, is the most stable phase. We have also generated pseudopotentials for the light actinides (Th, Pa, U and Np). We have study their phase transitions under pressure at zero temperature. We compared our results with all electron results. The structure parameters have always been relaxed in this study. And for the first time in pseudopotential calculation, the spin-orbit coupling has been taken into account. The curves describing the variation of the volume or the incompressibility modulus depending on the elements and the phase transitions are always in agreement with the one found in the all electron calculations. (author)

  17. Transmutation prospect of long-lived nuclear waste induced by high-charge electron beam from laser plasma accelerator

    Science.gov (United States)

    Wang, X. L.; Xu, Z. Y.; Luo, W.; Lu, H. Y.; Zhu, Z. C.; Yan, X. Q.

    2017-09-01

    Photo-transmutation of long-lived nuclear waste induced by a high-charge relativistic electron beam (e-beam) from a laser plasma accelerator is demonstrated. A collimated relativistic e-beam with a high charge of approximately 100 nC is produced from high-intensity laser interaction with near-critical-density (NCD) plasma. Such e-beam impinges on a high-Z convertor and then radiates energetic bremsstrahlung photons with flux approaching 1011 per laser shot. Taking a long-lived radionuclide 126Sn as an example, the resulting transmutation reaction yield is the order of 109 per laser shot, which is two orders of magnitude higher than obtained from previous studies. It is found that at lower densities, a tightly focused laser irradiating relatively longer NCD plasmas can effectively enhance the transmutation efficiency. Furthermore, the photo-transmutation is generalized by considering mixed-nuclide waste samples, which suggests that the laser-accelerated high-charge e-beam could be an efficient tool to transmute long-lived nuclear waste.

  18. PHISICS TOOLKIT: MULTI-REACTOR TRANSMUTATION ANALYSIS UTILITY - MRTAU

    Energy Technology Data Exchange (ETDEWEB)

    Andrea Alfonsi; Cristian Rabiti; Aaron S. Epiney; Yaqi Wang; Joshua Cogliati

    2012-04-01

    The principal idea of this paper is to present the new capabilities available in the PHISICS toolkit, connected with the implementation of the depletion code MRTAU, a generic depletion/ decay/burn-up code developed at the Idaho National Laboratory. It is programmed in a modular structure and modern FORTRAN 95/2003. The code tracks the time evolution of the isotopic concentration of a given material accounting for nuclear reaction happening in presence of neutron flux and also due to natural decay. MRTAU has two different methods to perform the depletion calculation, in order to let the user choose the best one respect his needs. Both the methodologies and some significant results are reported in this paper.

  19. Fission fragment angular distributions in pre-actinide nuclei

    Science.gov (United States)

    Banerjee, Tathagata; Nath, S.; Jhingan, A.; Kaur, Gurpreet; Dubey, R.; Yadav, Abhishek; Laveen, P. V.; Shamlath, A.; Shareef, M.; Gehlot, J.; Saneesh, N.; Prasad, E.; Sugathan, P.; Pal, Santanu

    2016-10-01

    Background: Complete fusion of two nuclei leading to formation of a heavy compound nucleus (CN) is known to be hindered by various fission-like processes, in which the composite system reseparates after capture of the target and the projectile inside the potential barrier. As a consequence of these non-CN fission (NCNF) processes, fusion probability (PCN) starts deviating from unity. Despite substantial progress in understanding, the onset and the experimental signatures of NCNF and the degree of its influence on fusion have not yet been unambiguously identified. Purpose: This work aims to investigate the presence of NCNF, if any, in pre-actinide nuclei by systematic study of fission angular anisotropies and fission cross sections (σfis) in a number of nuclear reactions carried out at and above the Coulomb barrier (VB) . Method: Fission fragment angular distributions were measured for six 28Si-induced reactions involving isotopically enriched targets of 169Tm,176Yb,175Lu,180Hf,181Ta, and 182W leading to probable formation of CN in the pre-actinide region, at a laboratory energy (Elab) range of 129-146 MeV. Measurements were performed with large angular coverage (θlab=41∘ -170∘) in which fission fragments (FFs) were detected by nine hybrid telescope (E -Δ E ) detectors. Extracted fission angular anisotropies and σfis were compared with statistical model (SM) predictions. Results: Barring two reactions involving targets with large non-zero ground state spin (J ) , viz., 175Lu(7/2+) and 181Ta(7/2+) , experimental fission angular anisotropies were found to be higher in comparison with predictions of the statistical saddle point model (SSPM), at Ec .m . near VB. Comparison of present results with those from neighboring systems revealed that experimental anisotropies increasingly deviated from SSPM predictions as one moved from pre-actinide to actinide nuclei. For reactions involving targets with large nonzero J , this deviation was subdued. Comparison between

  20. Burning minor actinides in a HTR energy spectrum and effects on the final radiotoxicity

    Energy Technology Data Exchange (ETDEWEB)

    Pohl, Christoph, E-mail: christoph.pohl@de.tuv.com [Forschungszentrum Juelich GmbH, 52425 Juelich (Germany); Allelein, Hans-Josef [Forschungszentrum Juelich GmbH, 52425 Juelich (Germany)

    2012-10-15

    The production of nuclear energy with existing nuclear reactors is equivalent to the use of low enriched uranium. But the neutron capture of the large corresponding U-238 fuel fraction also generates a build-up of plutonium isotopes and minor actinides as Neptunium, Americium and Curium. These actinides are dominant for the long time assessment of final disposal therefore a minimization of the long living isotopes is aspired. Burning the actinides in a high temperature helium cooled graphite moderated reactor (HTR) is one of these options. Using plutonium isotopes to sustain the criticality of the system is intended to avoid highly enriched uranium because of international regulations and low enriched uranium because of the build up of new actinides from neutron capture in U-238. Also fractions of plutonium isotopes are build up to minor actinides but for this absorption the overall number of actinides keeps constant. Nevertheless for the final assessment the activity and toxicity of all important actinides have to be taken into account. This paper comprises calculations for plutonium/minor actinides/thorium fuel compositions, their correlated final burn-up and the long term activity and toxicity for a generic pebble bed HTR based on the reference design of the 400 MW PBMR. In particular the behaviour of the different minor actinide isotopes in the higher thermal energy spectrum of a HTR will be discussed. Thorium based fuel - as a promising alternative to uranium based fuel - offers several advantages as a minimized build up of new Pu and MA, a higher thermal conductivity and melting point. Combining the thorium fuel with a significant fraction of minor actinides and an isotope fraction consistent with burned LWR fuel the total amount of the minor actinides stays nearly unchanged while the isotope composition significantly changes. This behaviour with respect to the initial heavy metal load and the influence on the long term activity and toxicity will be discussed.

  1. Transmutation Analysis of Enriched Uranium and Deep Burn High Temperature Reactors

    Energy Technology Data Exchange (ETDEWEB)

    Michael A. Pope

    2012-07-01

    High temperature reactors (HTRs) have been under consideration for production of electricity, process heat, and for destruction of transuranics for decades. As part of the transmutation analysis efforts within the Fuel Cycle Research and Development (FCR&D) campaign, a need was identified for detailed discharge isotopics from HTRs for use in the VISION code. A conventional HTR using enriched uranium in UCO fuel was modeled having discharge burnup of 120 GWd/MTiHM. Also, a deep burn HTR (DB-HTR) was modeled burning transuranic (TRU)-only TRU-O2 fuel to a discharge burnup of 648 GWd/MTiHM. For each of these cases, unit cell depletion calculations were performed with SCALE/TRITON. Unit cells were used to perform this analysis using SCALE 6.1. Because of the long mean free paths (and migration lengths) of neutrons in HTRs, using a unit cell to represent a whole core can be non-trivial. The sizes of these cells were first set by using Serpent calculations to match a spectral index between unit cell and whole core domains. In the case of the DB-HTR, the unit cell which was arrived at in this way conserved the ratio of fuel to moderator found in a single block of fuel. In the conventional HTR case, a larger moderator-to-fuel ratio than that of a single block was needed to simulate the whole core spectrum. Discharge isotopics (for 500 nuclides) and one-group cross-sections (for 1022 nuclides) were delivered to the transmutation analysis team. This report provides documentation for these calculations. In addition to the discharge isotopics, one-group cross-sections were provided for the full list of 1022 nuclides tracked in the transmutation library.

  2. A Los Alamos concept for accelerator transmutation of waste and energy production (ATW)

    Energy Technology Data Exchange (ETDEWEB)

    1990-12-31

    This document contains the diagrams presented at the ATW (Accelerator Transmutation of Waste and Energy Production) External Review, December 10-12, 1990, held at Los Alamos National Laboratory. Included are the charge to the committee and the presentations for the committee`s review. Topics of the presentations included an overview of the concept, LINAC technology, near-term application -- high-level defense wastes (intense thermal neutron source, chemistry and materials), advanced application of the ATW concept -- fission energy without a high-level waste stream (overview, advanced technology, and advanced chemistry), and a summary of the research issues.

  3. Migration and accumulation at dislocations of transmutation helium in austenitic steels upon neutron irradiation

    Science.gov (United States)

    Kozlov, A. V.; Portnykh, I. A.

    2016-04-01

    The model of the migration and accumulation at dislocations of transmutation helium and the formation of helium-vacancy pore nuclei in austenitic steels upon neutron irradiation has been proposed. As illustrations of its application, the dependences of the characteristics of pore nuclei on the temperature of neutron irradiation have been calculated. The results of the calculations have been compared with the experimental data in the literature on measuring the characteristics of radiation-induced porosity that arises upon the irradiation of shells of fuel elements of a 16Cr-19Ni-2Mo-2Mn-Si-Ti-Nb-V-B steel in a fast BN600 neutron reactor at different temperatures.

  4. Transmutation of skyrmions to half-solitons driven by the nonlinear optical spin Hall effect.

    Science.gov (United States)

    Flayac, H; Solnyshkov, D D; Shelykh, I A; Malpuech, G

    2013-01-04

    We show that the spin domains, generated in the linear optical spin Hall effect by the analog of spin-orbit interaction for exciton polaritons, are associated with the formation of a Skyrmion lattice. In the nonlinear regime, the spin anisotropy of the polariton-polariton interactions results in a spatial compression of the domains and in a transmutation of the Skyrmions into oblique half-solitons. This phase transition is associated with both the focusing of the spin currents and the emergence of a strongly anisotropic emission pattern.

  5. Simulation for thick-target yields of transmutation reactions on radioactive targets, based on inverse kinematics

    Science.gov (United States)

    Ebata, Shuichiro; Aikawa, Masayuki; Imai, Shotaro

    2016-06-01

    To dispose of long-lived fission products (LLFP) ejected from nuclear reactor plants is one of the most important tasks on nuclear physics and engineering. The experiments with the radiative target are limited, due to the high radioactivity and chemical property of the target. In consequence, the nuclear reaction data for LLFP are insufficient. In this work, we propose a feasible method to obtain the data for radiative targets using inverse kinematics and simulate specific systems to evaluate the thick-target yields of the nuclear transmutation reactions for LLFP.

  6. Simulation for thick-target yields of transmutation reactions on radioactive targets, based on inverse kinematics

    Directory of Open Access Journals (Sweden)

    Ebata Shuichiro

    2016-01-01

    Full Text Available To dispose of long-lived fission products (LLFP ejected from nuclear reactor plants is one of the most important tasks on nuclear physics and engineering. The experiments with the radiative target are limited, due to the high radioactivity and chemical property of the target. In consequence, the nuclear reaction data for LLFP are insufficient. In this work, we propose a feasible method to obtain the data for radiative targets using inverse kinematics and simulate specific systems to evaluate the thick-target yields of the nuclear transmutation reactions for LLFP.

  7. Planning and reporting of Russian transmutation research projects within ISTC. Phase 2

    Energy Technology Data Exchange (ETDEWEB)

    Conde, H. [Uppsala Univ. (Sweden). Dept. of Neutron Research; Gudowski, W. [Royal Inst. of Tech., Stockholm (Sweden). Dept. of Reactor and Neutron Physics; Liljenzin, J.O. [Chalmers Univ. of Technology, Goeteborg (Sweden). Dept. of Nuclear Chemistry; Mileikovsky, C. [Pully (Switzerland)

    1998-11-01

    The present report about phase 2 of the SKI project on Planning and Reporting of Russian Transmutation Research Projects within ISTC is an update of the information given in the SKI report no 97:15 (Feb 1997) about phase 1 of the same project. The background information is partly repeated in the present report to avoid that the reader has to go back to the report of Phase 1 for information about the basis for the project. USA, EU, Japan, Republic of Korea and Norway are at present supporting the International Scientific and Technical Center (ISTC) in Moscow. The Centre gives funds to research projects of civilian interest to former nuclear weapon laboratories to counteract the risk of nuclear weapon proliferation by the emigration of former USSR technical and scientific experts to `border countries` which are aiming towards the development of nuclear weapons. Before Sweden and Finland entered the EU, both countries gave national support to ISTC, in the case of Sweden 4 MUSD. Some of the projects which were funded by the Swedish national support to ISTC are still in progress. Nuclear technical concepts (i.e. Accelerator Transmutation of Nuclear Waste, ATW) have been proposed to incinerate and transmute long-lived radioactive nuclear waste to relax the time needed to store the waste in a geological repository. The named Russian experts are knowledgeable and well equipped of doing research in the different technical fields of relevance for the transmutation concepts. Thus, a number of ISTC projects have been initiated, and further ones have been proposed, to investigate different technical aspects of ATW with a result that a fair number of former weapon specialists have converted from military to peaceful civilian research. A similar centre STCU (The Scientific and Technical Centre of the Ukraine) has been set up in Kiev. Sweden has been active in promoting this Centre, which is supported by USA, Japan, Canada and recently also by EU. The present report describes the

  8. Robert Boyle, Transmutation, and the History of Chemistry before Lavoisier: A Response to Kuhn.

    Science.gov (United States)

    Newman, William R

    2014-01-01

    In an influential article of 1952, Thomas Kuhn argued that Robert Boyle had little or no influence on the subsequent development of chemistry. This essay challenges Kuhn's view on two fronts. First, it shows that Johann Joachim Becher developed his hierarchical matter theory under the influence of Boyle and then transmitted it to the founder of the phlogiston theory, G. E. Stahl. Second, this essay argues that transmutational matter theories were not necessarily opposed to the existence of stable chemical species, pace Kuhn. Boyle's corpuscular theory descended largely from the tradition of "chymical atomism," which often advocated both chrysopoeia and the reality of robust chemical substances.

  9. Transmuted Fréchet Distribution for growth hormone during acute sleep deprivation

    Directory of Open Access Journals (Sweden)

    Geetha. T

    2016-11-01

    Full Text Available New parameters can be introduced to expand families of distributions for added flexibility or to construct covariate models and this could be done in various ways. In this paper we use Transmuted Fréchet Distribution to find GH response in sleep deprived individuals. The effect of acute sleep deprivation on exercise-induced growth hormoneand insulin-like growth factor-1 was examined. Ten mencompleted two randomized 24-h sessions including a brief,high-intensity exercise bout following either a night of sleep or sleep deprivation

  10. Multivariate data analysis of process control data from neutron transmutation doping of silicon

    DEFF Research Database (Denmark)

    Heydorn, K.; Hegaard, N.

    1994-01-01

    Final resistivities obtained by neutron transmutation doping (NTD) of silicon can be measured only after an annealing process has been carried out at the manufacturer's plant. The reactor centre carrying out the neutron doping process by irradiation under selected conditions must control the proc...... the process by indirect measurement of the product quality. The method of partial least squares was used to identify important parameters for improving the quality of the NTD-silicon, as well as for predicting the final quality data observed by the customer....

  11. Computational Neutronics Methods and Transmutation Performance Analyses for Fast Reactors

    Energy Technology Data Exchange (ETDEWEB)

    R. Ferrer; M. Asgari; S. Bays; B. Forget

    2007-03-01

    The once-through fuel cycle strategy in the United States for the past six decades has resulted in an accumulation of Light Water Reactor (LWR) Spent Nuclear Fuel (SNF). This SNF contains considerable amounts of transuranic (TRU) elements that limit the volumetric capacity of the current planned repository strategy. A possible way of maximizing the volumetric utilization of the repository is to separate the TRU from the LWR SNF through a process such as UREX+1a, and convert it into fuel for a fast-spectrum Advanced Burner Reactor (ABR). The key advantage in this scenario is the assumption that recycling of TRU in the ABR (through pyroprocessing or some other approach), along with a low capture-to-fission probability in the fast reactor’s high-energy neutron spectrum, can effectively decrease the decay heat and toxicity of the waste being sent to the repository. The decay heat and toxicity reduction can thus minimize the need for multiple repositories. This report summarizes the work performed by the fuel cycle analysis group at the Idaho National Laboratory (INL) to establish the specific technical capability for performing fast reactor fuel cycle analysis and its application to a high-priority ABR concept. The high-priority ABR conceptual design selected is a metallic-fueled, 1000 MWth SuperPRISM (S-PRISM)-based ABR with a conversion ratio of 0.5. Results from the analysis showed excellent agreement with reference values. The independent model was subsequently used to study the effects of excluding curium from the transuranic (TRU) external feed coming from the LWR SNF and recycling the curium produced by the fast reactor itself through pyroprocessing. Current studies to be published this year focus on analyzing the effects of different separation strategies as well as heterogeneous TRU target systems.

  12. Gas Generation from Actinide Oxide Materials

    Energy Technology Data Exchange (ETDEWEB)

    George Bailey; Elizabeth Bluhm; John Lyman; Richard Mason; Mark Paffett; Gary Polansky; G. D. Roberson; Martin Sherman; Kirk Veirs; Laura Worl

    2000-12-01

    This document captures relevant work performed in support of stabilization, packaging, and long term storage of plutonium metals and oxides. It concentrates on the issue of gas generation with specific emphasis on gas pressure and composition. Even more specifically, it summarizes the basis for asserting that materials loaded into a 3013 container according to the requirements of the 3013 Standard (DOE-STD-3013-2000) cannot exceed the container design pressure within the time frames or environmental conditions of either storage or transportation. Presently, materials stabilized and packaged according to the 3013 Standard are to be transported in certified packages (the certification process for the 9975 and the SAFKEG has yet to be completed) that do not rely on the containment capabilities of the 3013 container. Even though no reliance is placed on that container, this document shows that it is highly likely that the containment function will be maintained not only in storage but also during transportation, including hypothetical accident conditions. Further, this document, by summarizing materials-related data on gas generation, can point those involved in preparing Safety Analysis Reports for Packages (SARPs) to additional information needed to assess the ability of the primary containment vessel to contain the contents and any reaction products that might reasonably be produced by the contents.

  13. Systematic Characteristics of Fast Neutron Fission Cross Sections for Actinide Nuclei

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    The neutron fission cross sections of actinide nuclei are important data for the design of nuclear reactor and nuclear engineering, and so on. So far, there has been a certain amount of experimental data for the fission cross sections of actinide nuclei. However,

  14. Invisible structures in the X-ray absorption spectra of actinides

    NARCIS (Netherlands)

    Kvashnina, Kristina O.; De Groot, Frank M F

    2014-01-01

    The X-ray absorption spectra of actinides are discussed with an emphasis on the fundamental effects that influence their spectral shape, including atomic multiplet theory, charge transfer theory and crystal field theory. Many actinide spectra consist of a single peak and it is shown that the use of

  15. Hybrid conducting polymer materials incorporating poly-oxo-metalates for extraction of actinides; Materiaux polymeres conducteurs hybrides incorporant des polyoxometallates pour l'extraction d'actinides

    Energy Technology Data Exchange (ETDEWEB)

    Racimor, D

    2003-09-15

    The preparation and characterization of hybrid conducting polymers incorporating poly-oxo-metalates for extracting actinides is discussed. A study of the coordination of various lanthanide cations (Ce(III), Ce(IV), Nd(III)) by the mono-vacant poly-oxo-metalate {alpha}{sub 2}-[P{sub 2}W{sub 17}O{sub 61}]{sup 10-} showed significant differences according to the cation.. Various {alpha}-A-[PW{sub 9}O{sub 34}(RPO){sub 2}]{sup 5-} hybrids were synthesized and their affinity for actinides or lanthanides was demonstrated through complexation. The first hybrid poly-oxo-metallic lanthanide complexes were then synthesized, as was the first hybrid functionalized with a pyrrole group. The electro-polymerization conditions of this pyrrole remain still to be optimized. Poly-pyrrole materials incorporating {alpha}{sub 2}-[P{sub 2}W{sub 17}O{sub 61}]{sup 10-} or its neodymium or cerium complexes as doping agents proved to be the first conducting polymer incorporating poly-oxo-metalates capable of extracting plutonium from nitric acid. (author)

  16. System for Nuclear Waste Transmutation Driven by Target-Distributed Accelerators

    OpenAIRE

    Blanovsky, Anatoly

    2004-01-01

    A design concept and characteristics for an epithermal breeder controlled by variable feedback and external neutron source intensity are presented. By replacing the control rods with neutron sources, we could improve safety and perform radioactive waste burning in high flux subcritical reactors (HFSR). To increase neutron source intensity the HFSR is divided into two zones: a booster and a blanket operating with solid and liquid fuels. Use of a liquid actinide fuel permits transport of the de...

  17. Studies on the properties of hard-spectrum, actinide fissioning reactors. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Nelson, J.B.; Prichard, A.W.; Schofield, P.E.; Robinson, A.H.; Spinrad, B.I.

    1980-01-01

    It is technically feasible to construct an operable (e.g., safe and stable) reactor to burn waste actinides rapidly. The heart of the concept is a driver core of EBR-II type, with a central radial target zone in which fuel elements, made entirely of waste actinides are exposed. This target fuel undergoes fission, as a result of which actinides are rapidly destroyed. Although the same result could be achieved in more conventionally designed LWR or LMFBR systems, the fast spectrum reactor does a much more efficient job, by virtue of the fact that in both LWR and LMFBR reactors, actinide fission is preceded by several captures before a fissile nuclide is formed. In the fast spectrum reactor that is called ABR (actinide burning reactor), these neutron captures are short-circuited.

  18. MINOR ACTINIDE SEPARATIONS USING ION EXCHANGERS OR IONIC LIQUIDS

    Energy Technology Data Exchange (ETDEWEB)

    Hobbs, D.; Visser, A.; Bridges, N.

    2011-09-20

    This project seeks to determine if (1) inorganic-based ion exchange materials or (2) electrochemical methods in ionic liquids can be exploited to provide effective Am and Cm separations. Specifically, we seek to understand the fundamental structural and chemical factors responsible for the selectivity of inorganic-based ion-exchange materials for actinide and lanthanide ions. Furthermore, we seek to determine whether ionic liquids can serve as the electrolyte that would enable formation of higher oxidation states of Am and other actinides. Experiments indicated that pH, presence of complexants and Am oxidation state exhibit significant influence on the uptake of actinides and lanthanides by layered sodium titanate and hybrid zirconium and tin phosphonate ion exchangers. The affinity of the ion exchangers increased with increasing pH. Greater selectivity among Ln(III) ions with sodium titanate materials occurs at a pH close to the isoelectric potential of the ion exchanger. The addition of DTPA decreased uptake of Am and Ln, whereas the addition of TPEN generally increases uptake of Am and Ln ions by sodium titanate. Testing confirmed two different methods for producing Am(IV) by oxidation of Am(III) in ionic liquids (ILs). Experimental results suggest that the unique coordination environment of ionic liquids inhibits the direct electrochemical oxidation of Am(III). The non-coordinating environment increases the oxidation potential to a higher value, while making it difficult to remove the inner coordination of water. Both confirmed cases of Am(IV) were from the in-situ formation of strong chemical oxidizers.

  19. Impurities that cause difficulty in stripping actinides from commercial tetraalkylcarbamoylmethylphosphonates

    Energy Technology Data Exchange (ETDEWEB)

    Bahner, C. T.; Shoun, R. R.; McDowell, W. J.

    1977-09-01

    Dihexyl((diethylcarbamoyl)methyl)phosphonate (DHDECMP) in diethylbenzene extracts actinides well from 6 M nitric acid solution, but commercially available DHDECMP contains impurities which interfere with stripping the actinides from the organic extract. DHDECMP purified by molecular distillation does not contain these impurities, but the pot residue contains increased concentrations of them. Heating the purified DHDECMP causes the formation of products which interfere with stripping in the same way, suggesting that high temperatures employed in the manufacture of DHDECMP may produce the offending impurities. These impurities can be separated from the heat-decomposed material or the pot residues by dilution with a large volume of hexanes (causing part of the impurities to separate as a second liquid phase) followed by equilibration of the hexane solution with dilute alkali. After the treatment with hexane and dilute alkali, the DHDECMP is readily recovered and functions well in the actinide extraction process. Dibutyl((dibutylcarbamoyl)methyl)-phosphonate (DBDBCMP) and di(2-ethylhexyl)((diethylcarbamoyl)-methyl)phosphonate (DEHDECMP) are purified less effectively by these methods. Similar separation methods using diethylbenzene or CCl/sub 4/ as solvent do not remove impurities as completely as the hexane process. Impurities can also be removed from a benzene solution of the DHDECMP pot residue by passing it through a column packed with silica gel or diethylaminoethyl cellulose. These impurities have been separated into fractions for analytical examination by use of various solvents and by column chromatography. Hexyl hydrogen ((diethylcarbamoyl)methyl)-phosphonate has been identified tentatively as a principal objectionable impurity. Dihexyl phosphoric acid and possibly dihexylphosphonate have been identified in other fractions.

  20. Final Report on Actinide Glass Scintillators for Fast Neutron Detection

    Energy Technology Data Exchange (ETDEWEB)

    Bliss, Mary; Stave, Jean A.

    2012-10-01

    This is the final report of an experimental investigation of actinide glass scintillators for fast-neutron detection. It covers work performed during FY2012. This supplements a previous report, PNNL-20854 “Initial Characterization of Thorium-loaded Glasses for Fast Neutron Detection” (October 2011). The work in FY2012 was done with funding remaining from FY2011. As noted in PNNL-20854, the glasses tested prior to July 2011 were erroneously identified as scintillators. The decision was then made to start from “scratch” with a literature survey and some test melts with a non-radioactive glass composition that could later be fabricated with select actinides, most likely thorium. The normal stand-in for thorium in radioactive waste glasses is cerium in the same oxidation state. Since cerium in the 3+ state is used as the light emitter in many scintillating glasses, the next most common substitute was used: hafnium. Three hafnium glasses were melted. Two melts were colored amber and a third was clear. It barely scintillated when exposed to alpha particles. The uses and applications for a scintillating fast neutron detector are important enough that the search for such a material should not be totally abandoned. This current effort focused on actinides that have very high neutron capture energy releases but low neutron capture cross sections. This results in very long counting times and poor signal to noise when working with sealed sources. These materials are best for high flux applications and access to neutron generators or reactors would enable better test scenarios. The total energy of the neutron capture reaction is not the only factor to focus on in isotope selection. Many neutron capture reactions result in energetic gamma rays that require large volumes or high densities to detect. If the scintillator is to separate neutrons from gamma rays, the capture reactions should produce heavy particles and few gamma rays. This would improve the detection of a