IMPROVED PROCESS OF PLUTONIUM CARRIER PRECIPITATION

Science.gov (United States)

Faris, B.F.

1959-06-30

This patent relates to an improvement in the bismuth phosphate process for separating and recovering plutonium from neutron irradiated uranium, resulting in improved decontamination even without the use of scavenging precipitates in the by-product precipitation step and subsequently more complete recovery of the plutonium in the product precipitation step. This improvement is achieved by addition of fluomolybdic acid, or a water soluble fluomolybdate, such as the ammonium, sodium, or potassium salt thereof, to the aqueous nitric acid solution containing tetravalent plutonium ions and contaminating fission products, so as to establish a fluomolybdate ion concentration of about 0.05 M. The solution is then treated to form the bismuth phosphate plutonium carrying precipitate.

Magnetic separation as a plutonium residue enrichment process

International Nuclear Information System (INIS)

Avens, L.R.; Gallegos, U.F.; McFarlan, J.T.

1990-01-01

Several plutonium contaminated residues have been subjected to Open Gradient Magnetic Separation (OGMS) on an experimental scale. OGMS experiments on graphite and bomb reduction residues resulted in a plutonium rich fraction and a plutonium lean fraction. Values for the bulk quantity rejected to the lean fraction varied between about 20% to 85% of the feed bulk. The plutonium content of the lean fraction can be reduced from about 2% in the feed to the 0.1% to 0.5% range dependent on the portion of the feed rejected to this lean fraction. These values are low enough in plutonium to meet economic discard limits and be considered for direct discard. Magnetic separation of pyrochemical salts gave less favorable results. While a fraction very rich in plutonium could be obtained, the lean fraction plutonium content was too high for direct discard. This may still have chemical processing applications. OGMS experiments at low magnetic field strength on incinerator ash did give two fractions but the plutonium content of each fraction was essentially identical. Thus, no chemical processing advantage was identified for magnetic separation of this residue. 6 refs., 1 fig., 9 tabs

Continuous precipitation process of plutonium salts; Procede continu de precipitation des sels de plutonium

Energy Technology Data Exchange (ETDEWEB)

Richard, P [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

1967-03-01

This work concerns the continuous precipitation process of plutonium oxalate. Investigations about the solubility of different valence states in nitric-oxalic and in nitric-sulfuric-oxalic medium lead to select the precipitation process of tetravalent plutonium oxalate. Settling velocity and granulometry of tetravalent oxalate plutonium have been studied with variation of several precipitation parameters such as: temperature, acidity, excess of oxalic acid and aging time. Then are given test results of some laboratory continuous apparatus. Conditions of operation with adopted tubular apparatus are defined in conclusion. A flow-sheet is given for a process at industrial scale. (author) [French] Cette etude porte sur la precipitation continue de l'oxalate de plutonium. L'etude de la solubilite des differentes valences du plutonium dans des milieux acides nitrique-oxalique, puis nitrique-sulfurique-oxalique conduit a choisir la precipitation de l'oxalate de plutonium tetravalent. L'etude porte ensuite sur la sedimentation et la granulometrie de l'oxalate de Pu{sup 4+} obtenue en faisant varier differents parametres de la precipitation : la temperature, l'acidite, l'exces oxalique et le temps de murissement. La derniere partie traite des resultats obtenus avec plusieurs types d'appareils continus essayes au laboratoire. En conclusion sont donnees les conditions de marche de l'appareil tubulaire adopte, ainsi qu'une extrapolation a l'echelle industrielle sous forme d'un flow-sheet. (auteur)

Weapons-grade plutonium dispositioning. Volume 4

International Nuclear Information System (INIS)

Sterbentz, J.W.; Olsen, C.S.; Sinha, U.P.

1993-06-01

This study is in response to a request by the Reactor Panel Subcommittee of the National Academy of Sciences (NAS) Committee on International Security and Arms Control (CISAC) to evaluate the feasibility of using plutonium fuels (without uranium) for disposal in existing conventional or advanced light water reactor (LWR) designs and in low temperature/pressure LWR designs that might be developed for plutonium disposal. Three plutonium-based fuel forms (oxides, aluminum metallics, and carbides) are evaluated for neutronic performance, fabrication technology, and material and compatibility issues. For the carbides, only the fabrication technologies are addressed. Viable plutonium oxide fuels for conventional or advanced LWRs include plutonium-zirconium-calcium oxide (PuO 2 -ZrO 2 -CaO) with the addition of thorium oxide (ThO 2 ) or a burnable poison such as erbium oxide (Er 2 O 3 ) or europium oxide (Eu 2 O 3 ) to achieve acceptable neutronic performance. Thorium will breed fissile uranium that may be unacceptable from a proliferation standpoint. Fabrication of uranium and mixed uranium-plutonium oxide fuels is well established; however, fabrication of plutonium-based oxide fuels will require further development. Viable aluminum-plutonium metallic fuels for a low temperature/pressure LWR include plutonium aluminide in an aluminum matrix (PuAl 4 -Al) with the addition of a burnable poison such as erbium (Er) or europium (Eu). Fabrication of low-enriched plutonium in aluminum-plutonium metallic fuel rods was initially established 30 years ago and will require development to recapture and adapt the technology to meet current environmental and safety regulations. Fabrication of high-enriched uranium plate fuel by the picture-frame process is a well established process, but the use of plutonium would require the process to be upgraded in the United States to conform with current regulations and minimize the waste streams

Reclamation of plutonium from pyrochemical processing residues

International Nuclear Information System (INIS)

Gray, L.W.; Gray, J.H.; Holcomb, H.P.; Chostner, D.F.

1987-04-01

Savannah River Laboratory (SRL), Savannah River Plant (SRP), and Rocky Flats Plant (RFP) have jointly developed a process to recover plutonium from molten salt extraction residues. These NaCl, KCL, and MgCl 2 residues, which are generated in the pyrochemical extraction of 241 Am from aged plutonium metal, contain up to 25 wt % dissolved plutonium and up to 2 wt % americium. The overall objective was to develop a process to convert these residues to a pure plutonium metal product and discardable waste. To meet this objective a combination of pyrochemical and aqueous unit operations was used. The first step was to scrub the salt residue with a molten metal (aluminum and magnesium) to form a heterogeneous ''scrub alloy'' containing nominally 25 wt % plutonium. This unit operation, performed at RFP, effectively separated the actinides from the bulk of the chloride salts. After packaging in aluminum cans, the ''scrub alloy'' was then dissolved in a nitric acid - hydrofluoric acid - mercuric nitrate solution at SRP. Residual chloride was separated from the dissolver solution by precipitation with Hg 2 (NO 3 ) 2 followed by centrifuging. Plutonium was then separated from the aluminum, americium and magnesium using the Purex solvent extraction system. The 241 Am was diverted to the waste tank farm, but could be recovered if desired

Process for recovery of plutonium from fabrication residues of mixed fuels consisting of uranium oxide and plutonium oxide

International Nuclear Information System (INIS)

Heremanns, R.H.; Vandersteene, J.J.

1983-01-01

The invention concerns a process for recovery of plutonium from fabrication residues of mixed fuels consisting of uranium oxide and plutonium oxide in the form of PuO 2 . Mixed fuels consisting of uranium oxide and plutonium oxide are being used more and more. The plants which prepare these mixed fuels have around 5% of the total mass of fuels as fabrication residue, either as waste or scrap. In view of the high cost of plutonium, it has been attempted to recover this plutonium from the fabrication residues by a process having a purchase price lower than the price of plutonium. The problem is essentially to separate the plutonium, the uranium and the impurities. The residues are fluorinated, the UF 6 and PuF 6 obtained are separated by selective absorption of the PuF 6 on NaF at a temperature of at least 400 0 C, the complex obtained by this absorption is dissolved in nitric acid solution, the plutonium is precipitated in the form of plutonium oxalate by adding oxalic acid, and the precipitated plutonium oxalate is calcined

Dynamic process model of a plutonium oxalate precipitator. Final report

Energy Technology Data Exchange (ETDEWEB)

Miller, C.L.; Hammelman, J.E.; Borgonovi, G.M.

1977-11-01

In support of LLL material safeguards program, a dynamic process model was developed which simulates the performance of a plutonium (IV) oxalate precipitator. The plutonium oxalate precipitator is a component in the plutonium oxalate process for making plutonium oxide powder from plutonium nitrate. The model is based on state-of-the-art crystallization descriptive equations, the parameters of which are quantified through the use of batch experimental data. The dynamic model predicts performance very similar to general Hanford oxalate process experience. The utilization of such a process model in an actual plant operation could promote both process control and material safeguards control by serving as a baseline predictor which could give early warning of process upsets or material diversion. The model has been incorporated into a FORTRAN computer program and is also compatible with the DYNSYS 2 computer code which is being used at LLL for process modeling efforts.

Dynamic process model of a plutonium oxalate precipitator. Final report

International Nuclear Information System (INIS)

Miller, C.L.; Hammelman, J.E.; Borgonovi, G.M.

1977-11-01

In support of LLL material safeguards program, a dynamic process model was developed which simulates the performance of a plutonium (IV) oxalate precipitator. The plutonium oxalate precipitator is a component in the plutonium oxalate process for making plutonium oxide powder from plutonium nitrate. The model is based on state-of-the-art crystallization descriptive equations, the parameters of which are quantified through the use of batch experimental data. The dynamic model predicts performance very similar to general Hanford oxalate process experience. The utilization of such a process model in an actual plant operation could promote both process control and material safeguards control by serving as a baseline predictor which could give early warning of process upsets or material diversion. The model has been incorporated into a FORTRAN computer program and is also compatible with the DYNSYS 2 computer code which is being used at LLL for process modeling efforts

The benefits of an advanced fast reactor fuel cycle for plutonium management

International Nuclear Information System (INIS)

Hannum, W.H.; McFarlane, H.F.; Wade, D.C.; Hill, R.N.

1996-01-01

The United States has no program to investigate advanced nuclear fuel cycles for the large-scale consumption of plutonium from military and civilian sources. The official U.S. position has been to focus on means to bury spent nuclear fuel from civilian reactors and to achieve the spent fuel standard for excess separated plutonium, which is considered by policy makers to be an urgent international priority. Recently, the National Research Council published a long awaited report on its study of potential separation and transmutation technologies (STATS), which concluded that in the nuclear energy phase-out scenario that they evaluated, transmutation of plutonium and long-lived radioisotopes would not be worth the cost. However, at the American Nuclear Society Annual Meeting in June, 1996, the STATS panelists endorsed further study of partitioning to achieve superior waste forms for burial, and suggested that any further consideration of transmutation should be in the context of energy production, not of waste management. 2048 The U.S. Department of Energy (DOE) has an active program for the short-term disposition of excess fissile material and a 'focus area' for safe, secure stabilization, storage and disposition of plutonium, but has no current programs for fast reactor development. Nevertheless, sufficient data exist to identify the potential advantages of an advanced fast reactor metallic fuel cycle for the long-term management of plutonium. Advantages are discussed

Dry sample storage system for an analytical laboratory supporting plutonium processing

International Nuclear Information System (INIS)

Treibs, H.A.; Hartenstein, S.D.; Griebenow, B.L.; Wade, M.A.

1990-01-01

The Special Isotope Separation (SIS) plant is designed to provide removal of undesirable isotopes in fuel grade plutonium by the atomic vapor laser isotope separation (AVLIS) process. The AVLIS process involves evaporation of plutonium metal, and passage of an intense beam of light from a laser through the plutonium vapor. The laser beam consists of several discrete wavelengths, tuned to the precise wavelength required to ionize the undesired isotopes. These ions are attracted to charged plates, leaving the bulk of the plutonium vapor enriched in the desired isotopes to be collected on a cold plate. Major portions of the process consist of pyrochemical processes, including direct reduction of the plutonium oxide feed material with calcium metal, and aqueous processes for purification of plutonium in residues. The analytical laboratory for the plant is called the Material and Process Control Laboratory (MPCL), and provides for the analysis of solid and liquid process samples

Study of plutonium disposition using the GE Advanced Boiling Water Reactor (ABWR)

Energy Technology Data Exchange (ETDEWEB)

NONE

1994-04-30

The end of the cold war and the resulting dismantlement of nuclear weapons has resulted in the need for the U.S. to disposition 50 to 100 metric tons of excess of plutonium in parallel with a similar program in Russia. A number of studies, including the recently released National Academy of Sciences (NAS) study, have recommended conversion of plutonium into spent nuclear fuel with its high radiation barrier as the best means of providing long-term diversion resistance to this material. The NAS study {open_quotes}Management and Disposition of Excess Weapons Plutonium{close_quotes} identified light water reactor spent fuel as the most readily achievable and proven form for the disposition of excess weapons plutonium. The study also stressed the need for a U.S. disposition program which would enhance the prospects for a timely reciprocal program agreement with Russia. This summary provides the key findings of a GE study where plutonium is converted into Mixed Oxide (MOX) fuel and a 1350 MWe GE Advanced Boiling Water Reactor (ABWR) is utilized to convert the plutonium to spent fuel. The ABWR represents the integration of over 30 years of experience gained worldwide in the design, construction and operation of BWRs. It incorporates advanced features to enhance reliability and safety, minimize waste and reduce worker exposure. For example, the core is never uncovered nor is any operator action required for 72 hours after any design basis accident. Phase 1 of this study was documented in a GE report dated May 13, 1993. DOE`s Phase 1 evaluations cited the ABWR as a proven technical approach for the disposition of plutonium. This Phase 2 study addresses specific areas which the DOE authorized as appropriate for more in-depth evaluations. A separate report addresses the findings relative to the use of existing BWRs to achieve the same goal.

Design of plutonium processing facilities

International Nuclear Information System (INIS)

Derbyshire, W.; Sills, R.J.

1982-01-01

Five considerations for the design of plutonium processing facilities are identified. These are: Toxicity, Radiation, Criticality, Containment and Remote Operation. They are examined with reference to reprocessing spent nuclear fuel and application is detailed both for liquid and dry processes. (author)

Study of plutonium disposition using existing GE advanced Boiling Water Reactors

Energy Technology Data Exchange (ETDEWEB)

1994-06-01

The end of the cold war and the resulting dismantlement of nuclear weapons has resulted in the need for the US to dispose of 50 to 100 metric tons of excess of plutonium in a safe and proliferation resistant manner. A number of studies, including the recently released National Academy of Sciences (NAS) study, have recommended conversion of plutonium into spent nuclear fuel with its high radiation barrier as the best means of providing permanent conversion and long-term diversion resistance to this material. The NAS study ``Management and Disposition of Excess Weapons Plutonium identified Light Water Reactor spent fuel as the most readily achievable and proven form for the disposition of excess weapons plutonium. The study also stressed the need for a US disposition program which would enhance the prospects for a timely reciprocal program agreement with Russia. This summary provides the key findings of a GE study where plutonium is converted into Mixed Oxide (MOX) fuel and a typical 1155 MWe GE Boiling Water Reactor (BWR) is utilized to convert the plutonium to spent fuel. A companion study of the Advanced BWR has recently been submitted. The MOX core design work that was conducted for the ABWR enabled GE to apply comparable fuel design concepts and consequently achieve full MOX core loading which optimize plutonium throughput for existing BWRs.

Study of plutonium disposition using existing GE advanced Boiling Water Reactors

International Nuclear Information System (INIS)

1994-01-01

The end of the cold war and the resulting dismantlement of nuclear weapons has resulted in the need for the US to dispose of 50 to 100 metric tons of excess of plutonium in a safe and proliferation resistant manner. A number of studies, including the recently released National Academy of Sciences (NAS) study, have recommended conversion of plutonium into spent nuclear fuel with its high radiation barrier as the best means of providing permanent conversion and long-term diversion resistance to this material. The NAS study ''Management and Disposition of Excess Weapons Plutonium identified Light Water Reactor spent fuel as the most readily achievable and proven form for the disposition of excess weapons plutonium. The study also stressed the need for a US disposition program which would enhance the prospects for a timely reciprocal program agreement with Russia. This summary provides the key findings of a GE study where plutonium is converted into Mixed Oxide (MOX) fuel and a typical 1155 MWe GE Boiling Water Reactor (BWR) is utilized to convert the plutonium to spent fuel. A companion study of the Advanced BWR has recently been submitted. The MOX core design work that was conducted for the ABWR enabled GE to apply comparable fuel design concepts and consequently achieve full MOX core loading which optimize plutonium throughput for existing BWRs

PROCESS OF ELIMINATING HYDROGEN PEROXIDE IN SOLUTIONS CONTAINING PLUTONIUM VALUES

Science.gov (United States)

Barrick, J.G.; Fries, B.A.

1960-09-27

A procedure is given for peroxide precipitation processes for separating and recovering plutonium values contained in an aqueous solution. When plutonium peroxide is precipitated from an aqueous solution, the supernatant contains appreciable quantities of plutonium and peroxide. It is desirable to process this solution further to recover plutonium contained therein, but the presence of the peroxide introduces difficulties; residual hydrogen peroxide contained in the supernatant solution is eliminated by adding a nitrite or a sulfite to this solution.

Effect of compositional variation in plutonium on process shielding design

Energy Technology Data Exchange (ETDEWEB)

Brown, T.H.

1997-11-01

Radiation dose rate from plutonium with high {sup 239}Pu content varies with initial nuclidic content, radioactive decay time, and impurity elemental content. The two idealized states of old plutonium and clean plutonium, whose initial compositions are given, provide approximate upper and lower bounds on dose rate variation. Whole-body dose rates were calculated for the two composition states, using unshielded and shielded plutonium spheres of varying density. The dose rates from these variable density spheres are similar to those from expanded plutonium configurations encountered during processing. The dose location of 40 cm from the sphere center is representative of operator standoff for direct handling of plutonium inside a glove box. The results have shielding implications for glove boxes with only structurally inherent shielding, especially for processing of old plutonium in an expanded configuration. Further reduction in total dose rate by using lead to reduce photon dose rate is shown for two density cases representing compact and expanded plutonium configurations.

Effect of compositional variation in plutonium on process shielding design

International Nuclear Information System (INIS)

Brown, T.H.

1997-11-01

Radiation dose rate from plutonium with high 239 Pu content varies with initial nuclidic content, radioactive decay time, and impurity elemental content. The two idealized states of old plutonium and clean plutonium, whose initial compositions are given, provide approximate upper and lower bounds on dose rate variation. Whole-body dose rates were calculated for the two composition states, using unshielded and shielded plutonium spheres of varying density. The dose rates from these variable density spheres are similar to those from expanded plutonium configurations encountered during processing. The dose location of 40 cm from the sphere center is representative of operator standoff for direct handling of plutonium inside a glove box. The results have shielding implications for glove boxes with only structurally inherent shielding, especially for processing of old plutonium in an expanded configuration. Further reduction in total dose rate by using lead to reduce photon dose rate is shown for two density cases representing compact and expanded plutonium configurations

Plutonium scrap processing at the Los Alamos Scientific Laboratory

International Nuclear Information System (INIS)

Nixon, A.E.; McKerley, B.J.; Christensen, E.L.

1980-01-01

The Los Alamos Scientific Laboratory currently has the newest plutonium handling facility in the nation. Los Alamos has been active in the processing of plutonium almost since the discovery of this man-made element in 1941. One of the functions of the new facility is the processing of plutonium scrap generated at LASL and other sites. The feed for the scrap processing program is extremely varied, and a wide variety of contaminants are often encountered. Depending upon the scrap matrix and contaminants present, the majority of material receives a nitric acid/hydrofluoric acid or nitric acid/calcium fluoride leach. The plutonium nitrate solutions are then loaded onto an anion exchange column charged with DOWEX 1 x 4, 50 to 100 mesh, nitrate form resin. The column is eluted with 0.48 M hydroxyl amine nitrate. The Pu(NO 3 ) 3 is then precipitated as plutonium III oxalate which is calcined at 450 to 500 0 C to yield a purified PuO 2 product

Impact of receipt of coprocessed uranium/plutonium on advanced accountability concepts and fabrication facilities. Addendum 1 to application of advanced accountability concepts in mixed oxide fabrication

International Nuclear Information System (INIS)

Bastin, J.J.; Jump, M.J.; Lange, R.A.; Randall, C.C.

1977-11-01

The Phase I study of the application of advanced accountability methods (DYMAC) in a uranium/plutonium mixed oxide facility was extended to assess the effect of coprocessed UO 2 --PuO 2 feed on the observations made in the original Phase I effort and on the proposed Phase II program. The retention of plutonium mixed with uranium throughout the process was also considered. This addendum reports that coprocessed feed would have minimal effect on the DYMAC program, except in the areas of material specifications, starting material delivery schedule, and labor requirements. Each of these areas is addressed, as are the impact of coprocessed feed at a large fuel fabrication facility and the changes needed in the dirty scrap recovery process to maintain the lower plutonium levels which may be required by future nonproliferation philosophy. An amended schedule for Phase II is included

PLUTONIUM PURIFICATION PROCESS EMPLOYING THORIUM PYROPHOSPHATE CARRIER

Science.gov (United States)

King, E.L.

1959-04-28

The separation and purification of plutonium from the radioactive elements of lower atomic weight is described. The process of this invention comprises forming a 0.5 to 2 M aqueous acidffc solution containing plutonium fons in the tetravalent state and elements with which it is normally contaminated in neutron irradiated uranium, treating the solution with a double thorium compound and a soluble pyrophosphate compound (Na/sub 4/P/sub 2/O/sub 7/) whereby a carrier precipitate of thorium A method is presented of reducing neptunium and - trite is advantageous since it destroys any hydrazine f so that they can be removed from solutions in which they are contained is described. In the carrier precipitation process for the separation of plutonium from uranium and fission products including zirconium and columbium, the precipitated blsmuth phosphate carries some zirconium, columbium, and uranium impurities. According to the invention such impurities can be complexed and removed by dissolving the contaminated carrier precipitate in 10M nitric acid, followed by addition of fluosilicic acid to about 1M, diluting the solution to about 1M in nitric acid, and then adding phosphoric acid to re-precipitate bismuth phosphate carrying plutonium.

Development of advanced spent fuel management process. System analysis of advanced spent fuel management process

International Nuclear Information System (INIS)

Ro, S.G.; Kang, D.S.; Seo, C.S.; Lee, H.H.; Shin, Y.J.; Park, S.W.

1999-03-01

The system analysis of an advanced spent fuel management process to establish a non-proliferation model for the long-term spent fuel management is performed by comparing the several dry processes, such as a salt transport process, a lithium process, the IFR process developed in America, and DDP developed in Russia. In our system analysis, the non-proliferation concept is focused on the separation factor between uranium and plutonium and decontamination factors of products in each process, and the non-proliferation model for the long-term spent fuel management has finally been introduced. (Author). 29 refs., 17 tabs., 12 figs

Conceptual Design for the Pilot-Scale Plutonium Oxide Processing Unit in the Radiochemical Processing Laboratory

Energy Technology Data Exchange (ETDEWEB)

Lumetta, Gregg J.; Meier, David E.; Tingey, Joel M.; Casella, Amanda J.; Delegard, Calvin H.; Edwards, Matthew K.; Jones, Susan A.; Rapko, Brian M.

2014-08-05

This report describes a conceptual design for a pilot-scale capability to produce plutonium oxide for use as exercise and reference materials, and for use in identifying and validating nuclear forensics signatures associated with plutonium production. This capability is referred to as the Pilot-scale Plutonium oxide Processing Unit (P3U), and it will be located in the Radiochemical Processing Laboratory at the Pacific Northwest National Laboratory. The key unit operations are described, including plutonium dioxide (PuO2) dissolution, purification of the Pu by ion exchange, precipitation, and conversion to oxide by calcination.

Advanced hybrid process with solvent extraction and pyro-chemical process of spent fuel reprocessing for LWR to FBR

International Nuclear Information System (INIS)

Fujita, Reiko; Mizuguchi, Koji; Fuse, Kouki; Saso, Michitaka; Utsunomiya, Kazuhiro; Arie, Kazuo

2008-01-01

Toshiba has been proposing a new fuel cycle concept of a transition from LWR to FBR. The new fuel cycle concept has better economical process of the LWR spent fuel reprocessing than the present Purex Process and the proliferation resistance for FBR cycle of plutonium with minor actinides after 2040. Toshiba has been developing a new Advanced Hybrid Process with Solvent Extraction and Pyrochemical process of spent fuel reprocessing for LWR to FBR. The Advanced Hybrid Process combines the solvent extraction process of the LWR spent fuel in nitric acid with the recovery of high pure uranium for LWR fuel and the pyro-chemical process in molten salts of impure plutonium recovery with minor actinides for metallic FBR fuel, which is the FBR spent fuel recycle system after FBR age based on the electrorefining process in molten salts since 1988. The new Advanced Hybrid Process enables the decrease of the high-level waste and the secondary waste from the spent fuel reprocessing plants. The R and D costs in the new Advanced Hybrid Process might be reduced because of the mutual Pyro-chemical process in molten salts. This paper describes the new fuel cycle concept of a transition from LWR to FBR and the feasibility of the new Advanced Hybrid Process by fundamental experiments. (author)

Plutonium production story at the Hanford site: processes and facilities history

Energy Technology Data Exchange (ETDEWEB)

Gerber, M.S., Westinghouse Hanford

1996-06-20

This document tells the history of the actual plutonium production process at the Hanford Site. It contains five major sections: Fuel Fabrication Processes, Irradiation of Nuclear Fuel, Spent Fuel Handling, Radiochemical Reprocessing of Irradiated Fuel, and Plutonium Finishing Operations. Within each section the story of the earliest operations is told, along with changes over time until the end of operations. Chemical and physical processes are described, along with the facilities where these processes were carried out. This document is a processes and facilities history. It does not deal with the waste products of plutonium production.

Fluid bed direct denitration process for plutonium nitrate to oxide conversion

International Nuclear Information System (INIS)

Souply, K.R.; Neal, D.H.

1977-01-01

The fluid bed direct-denitration process appears feasible for reprocessing Light Water Reactor fuel. Considerable experience with the fluid bed process exists in the denitration of uranyl nitrate and it shows promise for use in the denitration of plutonium nitrate. The process will require some development work before it can be used in a production-size facility. This report describes a fluid bed direct-denitration process for converting plutonium nitrate to plutonium oxide, and the information should be used when making comparisons of alternative processes or as a basis for further detailed studies

Screw calciner mechanical direct denitration process for plutonium nitrate to oxide conversion

International Nuclear Information System (INIS)

Souply, K.R.; Sperry, W.E.

1977-01-01

This report describes a screw calciner direct-denitration process for converting plutonium nitrate to plutonium oxide. The information should be used when making comparisons of alternative plutonium nitrate-to-oxide conversion processes or as a basis for further detailed studies. The report contains process flow sheets with a material balance; a process description; and a discussion of the process including history, advantages and disadvantages, and additional research required

Study on the process variables in the anion exchange plutonium separation process

Energy Technology Data Exchange (ETDEWEB)

Nishimura, D T

1957-11-15

This report discusses the study of the process variables in the Anion Exchange Process Pilot Plant for the separation of plutonium from irradiated uranium. Variables associated with the feed, wash and elution cycles were studied with the aim of improving the quality of the final plutonium product, reduce cycling time and reagent requirements, and also to obtain data for prediction of resin column behaviour under various feed conditions. A cation resin column and a silica gel column were installed in the system and these were studied for plutonium recovery and product quality. The product obtained from the plant was acceptable in all the impurities except the associated gamma activity which was too high for easy product handling. (author)

Liquid waste processing from plutonium (III) oxalate precipitation

International Nuclear Information System (INIS)

Esteban, A.; Cassaniti, P.; Orosco, E.H.

1990-01-01

Plutonium (III) oxalate filtrates contain about 0.2M oxalic acid, 0.09M ascorbic acid, 0.05M hydrazine, 1M nitric acid and 20-100 mg/l of plutonium. The developed treatment of liquid wastes consist in two main steps: a) Distillation to reduce up to 10% of the initial volume and refluxing to destroy organic material. Then, the treated solution is suitable to adjust the plutonium at the tetravalent state by addition of hydrogen peroxide and the nitric molarity up to 8.6M. b) Recovery and purification of plutonium by anion exchange using two columns in series containing Dowex 1-X4 resin. With the proposed process, it is possible to transform 38 litres of filtrates with 40mg/l of Pu into 0.1 l of purified solution with 15-20g/l of Pu. This solution is suitable to be recycled in the Pu (III) oxalate precipitation process. This process has several potential advantages over similar liquid waste treatments. These include: 1) It does not increase the liquid volume. 2) It consumes only few reagents. 3) The operations involved are simple, requiring limited handling and they are feasible to automatization. 4) The Pu recovery factor is about 99%. (Author) [es

The study of reductive reextraction of plutonium in the Purex process

International Nuclear Information System (INIS)

Poczynajlo, A.

1985-01-01

The methods of separation of U and Pu in the Purex process and the thermodynamic and kinetic properties of Pu(4) reductants are discussed. The kinetic equation of the process of reductive reextraction of plutonium for the first order reaction with respect to Pu(4) is derived. The kinetics of plutonium reextraction with the use of uranium (4), ascorbic acid and other reductants has been studied. The necessity of application of the stoichiometric excess of reductant has been explained by simultaneously occured reoxidation process of plutonium. The method of calculation of the steady- state plutonium concentration profiles has been elaborated for counter-current separation of U and Pu in multistage contactor. 90 refs., 20 tabs., 29 figs. (author)

Advanced plutonium management in PWR - complementarity of thorium and uranium cycles

International Nuclear Information System (INIS)

Ernoult, Marc

2014-01-01

In order to study the possibility of advanced management of plutonium in existing reactors, 8 strategies for plutonium multi-recycling in PWRs are studied. Following equilibrium studies, it was shown that, by using homogeneous assemblies, the use of thorium cannot reduce the plutonium inventory of equilibrium cycle or production of americium. By distributing the different fuel types within the same assembly, some thoriated strategies allow however lower inventories and lower production americium best strategies using only the uranium cycle. However, in all cases, low fuel conversion theories in PWRs makes it impossible to lower resource consumption more than a few percent compared to strategies without thorium. To study the transition, active participation in development of the scenario code CLASS has been taken. It led to the two simulation scenarios among those studied in equilibrium with CLASS. These simulations have shown discrepancies with previously simulated scenarios. The major causes of these differences were identified and quantified. (author)

Evaluation of the Magnesium Hydroxide Treatment Process for Stabilizing PFP Plutonium/Nitric Acid Solutions

Energy Technology Data Exchange (ETDEWEB)

Gerber, Mark A.; Schmidt, Andrew J.; Delegard, Calvin H.; Silvers, Kurt L.; Baker, Aaron B.; Gano, Susan R.; Thornton, Brenda M.

2000-09-28

This document summarizes an evaluation of the magnesium hydroxide [Mg(OH)2] process to be used at the Hanford Plutonium Finishing Plant (PFP) for stabilizing plutonium/nitric acid solutions to meet the goal of stabilizing the plutonium in an oxide form suitable for storage under DOE-STD-3013-99. During the treatment process, nitric acid solutions bearing plutonium nitrate are neutralized with Mg(OH)2 in an air sparge reactor. The resulting slurry, containing plutonium hydroxide, is filtered and calcined. The process evaluation included a literature review and extensive laboratory- and bench-scale testing. The testing was conducted using cerium as a surrogate for plutonium to identify and quantify the effects of key processing variables on processing time (primarily neutralization and filtration time) and calcined product properties.

Plutonium Finishing Plant. Interim plutonium stabilization engineering study

Energy Technology Data Exchange (ETDEWEB)

Sevigny, G.J.; Gallucci, R.H.; Garrett, S.M.K.; Geeting, J.G.H.; Goheen, R.S.; Molton, P.M.; Templeton, K.J.; Villegas, A.J. [Pacific Northwest Lab., Richland, WA (United States); Nass, R. [Nuclear Fuel Services, Inc. (United States)

1995-08-01

This report provides the results of an engineering study that evaluated the available technologies for stabilizing the plutonium stored at the Plutonium Finishing Plant located at the hanford Site in southeastern Washington. Further processing of the plutonium may be required to prepare the plutonium for interim (<50 years) storage. Specifically this document provides the current plutonium inventory and characterization, the initial screening process, and the process descriptions and flowsheets of the technologies that passed the initial screening. The conclusions and recommendations also are provided. The information contained in this report will be used to assist in the preparation of the environmental impact statement and to help decision makers determine which is the preferred technology to process the plutonium for interim storage.

Plutonium Finishing Plant. Interim plutonium stabilization engineering study

International Nuclear Information System (INIS)

Sevigny, G.J.; Gallucci, R.H.; Garrett, S.M.K.; Geeting, J.G.H.; Goheen, R.S.; Molton, P.M.; Templeton, K.J.; Villegas, A.J.; Nass, R.

1995-08-01

This report provides the results of an engineering study that evaluated the available technologies for stabilizing the plutonium stored at the Plutonium Finishing Plant located at the hanford Site in southeastern Washington. Further processing of the plutonium may be required to prepare the plutonium for interim (<50 years) storage. Specifically this document provides the current plutonium inventory and characterization, the initial screening process, and the process descriptions and flowsheets of the technologies that passed the initial screening. The conclusions and recommendations also are provided. The information contained in this report will be used to assist in the preparation of the environmental impact statement and to help decision makers determine which is the preferred technology to process the plutonium for interim storage

Aqueous recovery of plutonium from pyrochemical processing residues

International Nuclear Information System (INIS)

Gray, L.W.; Gray, J.H.

1984-01-01

Pyrochemical processes provide rapid methods to reclaim plutonium from scrap residues. Frequently, however, these processes yield an impure plutonium product and waste residues that are contaminated with actinides and are therefore nondiscardable. The Savannah River Laboratory and Plant and the Rocky Flats Plant are jointly developing new processes using both pyrochemistry and aqueous chemistry to generate pure product and discardable waste. An example of residue being treated is that from the molten salt extraction (MSE), a mixture of NaCl, KCl, MgCl 2 , PuCl 3 , AmCl 3 , PuO 2 , and Pu 0 . This mixture is scrubbed with molten aluminum containing a small amount of magnesium to produce a nonhomogeneous Al-Pu-Am-Mg alloy. This process, which rejects most of the NaCl-KCl-MgCl 2 salts, results in a product easily dissolved in 6M HNO 3 -0.1M HF. Any residual chloride in the product is removed by precipitation with Hg(I) followed by centrifuging. Plutonium and americium are then separated by the standard Purex process. The americium, initially diverted to the solvent extraction waste stream, can either be recovered or sent to waste

LITERATURE REVIEW FOR OXALATE OXIDATION PROCESSES AND PLUTONIUM OXALATE SOLUBILITY

Energy Technology Data Exchange (ETDEWEB)

Nash, C.

2012-02-03

A literature review of oxalate oxidation processes finds that manganese(II)-catalyzed nitric acid oxidation of oxalate in precipitate filtrate is a viable and well-documented process. The process has been operated on the large scale at Savannah River in the past, including oxidation of 20 tons of oxalic acid in F-Canyon. Research data under a variety of conditions show the process to be robust. This process is recommended for oxalate destruction in H-Canyon in the upcoming program to produce feed for the MOX facility. Prevention of plutonium oxalate precipitation in filtrate can be achieved by concentrated nitric acid/ferric nitrate sequestration of oxalate. Organic complexants do not appear practical to sequester plutonium. Testing is proposed to confirm the literature and calculation findings of this review at projected operating conditions for the upcoming campaign. H Canyon plans to commence conversion of plutonium metal to low-fired plutonium oxide in 2012 for eventual use in the Mixed Oxide Fuel (MOX) Facility. The flowsheet includes sequential operations of metal dissolution, ion exchange, elution, oxalate precipitation, filtration, and calcination. All processes beyond dissolution will occur in HB-Line. The filtration step produces an aqueous filtrate that may have as much as 4 M nitric acid and 0.15 M oxalate. The oxalate needs to be removed from the stream to prevent possible downstream precipitation of residual plutonium when the solution is processed in H Canyon. In addition, sending the oxalate to the waste tank farm is undesirable. This report addresses the processing options for destroying the oxalate in existing H Canyon equipment.

Ceramification: A plutonium immobilization process

Energy Technology Data Exchange (ETDEWEB)

Rask, W.C. [Dept. of Energy, Golden, CO (United States); Phillips, A.G. [Rocky Flats Environmental Technology Site, Golden, CO (United States)

1996-05-01

This paper describes a low temperature technique for stabilizing and immobilizing actinide compounds using a combination process/storage vessel of stainless steel, in which measured amounts of actinide nitrate solutions and actinide oxides (and/or residues) are systematically treated to yield a solid article. The chemical ceramic process is based on a coating technology that produces rare earth oxide coatings for defense applications involving plutonium. The final product of this application is a solid, coherent actinide oxide with process-generated encapsulation that has long-term environmental stability. Actinide compounds can be stabilized as pure materials for ease of re-use or as intimate mixtures with additives such as rare earth oxides to increase their degree of proliferation resistance. Starting materials for the process can include nitrate solutions, powders, aggregates, sludges, incinerator ashes, and others. Agents such as cerium oxide or zirconium oxide may be added as powders or precursors to enhance the properties of the resulting solid product. Additives may be included to produce a final product suitable for use in nuclear fuel pellet production. The process is simple and reduces the time and expense for stabilizing plutonium compounds. It requires a very low equipment expenditure and can be readily implemented into existing gloveboxes. The process is easily conducted with less associated risk than proposed alternative technologies.

PROCESS USING POTASSIUM LANTHANUM SULFATE FOR FORMING A CARRIER PRECIPITATE FOR PLUTONIUM VALUES

Science.gov (United States)

Angerman, A.A.

1958-10-21

A process is presented for recovering plutonium values in an oxidation state not greater than +4 from fluoride-soluble fission products. The process consists of adding to an aqueous acidic solution of such plutonium values a crystalline potassium lanthanum sulfate precipitate which carries the plutonium values from the solution.

The chemistry of plutonium in sol-gel processes

International Nuclear Information System (INIS)

Lloyd, M.H.; Haire, R.G.

1978-01-01

Studies of plutonium chemical behavior conducted in conjunction with plutonia sol-gel process development at ORNL are described. The colloidal solutions produced consist of 'Pu(IV) polymer,' and this is therefore the study of polymeric plutonium behavior. Spectrophotometric, electron diffraction, and electron microscopy studies, in addition to specific studies that were concerned with the colloidal behavior of Pu(IV) polymer, indicate several characteristics of polymer that are not generally recognized. The particle nature of Pu(IV) polymer indicated by electron microscopy, the amorphous-crystalline characteristics of primary polymer particles demonstrated by electron diffraction, and the reversible and irreversible aggregation of the primary particles shown by spectrophotometric techniques present a useful view of the nature of Pu(IV) polymer that has been helpful in solving or understanding various types of processing problems involving plutonium hydrolytic behavior. The colloidal characteristics of Pu(IV) polymer and crystallite growth of primary polymer particles by thermal denitration are also described. (orig.) [de

CONVERSION OF PLUTONIUM TRIFLUORIDE TO PLUTONIUM TETRAFLUORIDE

Science.gov (United States)

Fried, S.; Davidson, N.R.

1957-09-10

A large proportion of the trifluoride of plutonium can be converted, in the absence of hydrogen fluoride, to the tetrafiuoride of plutonium. This is done by heating plutonium trifluoride with oxygen at temperatures between 250 and 900 deg C. The trifiuoride of plutonium reacts with oxygen to form plutonium tetrafluoride and plutonium oxide, in a ratio of about 3 to 1. In the presence of moisture, plutonium tetrafluoride tends to hydrolyze at elevated temperatures and therefore it is desirable to have the process take place under anhydrous conditions.

Multiple recycling of plutonium in advanced PWRs

International Nuclear Information System (INIS)

Kloosterman, J.L.

1998-04-01

The influence of the moderator-to-fuel ratio in MOX fueled PWRs on the moderator void coefficient, the fuel temperature coefficient, the moderator temperature coefficient, the boron reactivity worth, the critical boron concentration, the mean neutron generation time and the effective delayed neutron fraction has been assessed. Increasing the moderator-to-fuel ratio to values larger than three, gives a moderator void coefficient sufficiently large to recycle the plutonium at least four times. Scenario studies show that four times recycling of plutonium in PWRs reduces the plutonium mass produced with a factor of three compared with a reference once-through reactor park, but that the americium and curium production triple. If the minor actinides and the remaining plutonium after four times recycling are disposed of, the reduction of the radiotoxicity reaches only a factor of two. This factor increases to five at the maximum when the plutonium is further recycled. Recycling of americium and curium is needed to further reduce the radiotoxicity of the spent fuel. 4 refs

In situ observation of plutonium transfer processes in the marine environment

International Nuclear Information System (INIS)

Guary, J.-C.; Fraizier, Andre

1975-09-01

A preliminary observation of plutonium transfer processes in the marine environment was carried out and showed that concentration of the radionuclide was lower when marine organisms stood at a higher trophic level. This observation supplemented by an investigation on contamination pathways showed that plutonium was not concentrated along the food chain and its uptake occured preferentially by direct contact of species with seawater, a process chiefly affecting producers and primary consumers. It appeared that the marine sediment was not a significant vector of plutonium transfer in burrowing species [fr

Advances on reverse strike co-precipitation method of uranium-plutonium mixed solutions

International Nuclear Information System (INIS)

Menghini, Jorge E.; Marchi, Daniel E.; Orosco, Edgardo H.; Greco, Luis

2000-01-01

The reverse strike coprecipitation of uranium-plutonium mixed solutions, is an alternative way to obtain MOX fuel pellets. Previous tests, carried out in the Alpha Laboratory, included a stabilization step for transforming 100 % of plutonium into Pu +4 . Therefore, the plutonium precipitated as Pu(OH) 4 . In this second step, the stabilization process was suppressed. In this way, besides Pu(OH) 4 , a part of the precipitated is composed of a mixed salt: AD(U,Pu). Then, a homogeneous solid solution is formed in the early steps of the process. The powders showed higher tap density, better performance during the pressing and lower sinterability than the powders obtained in previous tests. The advantageous and disadvantageous effects of the stabilization step are analyzed in this paper. (author)

EXPECTED IMPACT OF HANFORD PROCESSING ORGANICS OF PLUTONIUM DURING TANK WASTE SLUDGE RETRIEVAL

International Nuclear Information System (INIS)

TROYER, G.L.; WINTERS, W.I.

2004-01-01

This document evaluates the potential for extracting plutonium from Hanford waste tanks into residual organic solvents and how this process may have an impact on criticality specifications during the retrieval of wastes. The two controlling factors for concentrating plutonium are the solubility of the plutonium in the wastes and the extraction efficiency of the potential organic extractants that may be found in these wastes. Residual Hanford tank sludges contain plutonium in solid forms that are expected to be primarily insoluble Pu(IV) hydroxides. Evaluation of thermodynamic Pourbaix diagrams, documentation on solubility studies of various components in waste tank matrices, and actual analysis of plutonium in tank supernates all indicate that the solubility of Pu in the alkaline waste is on the order of 10 -6 M. Based on an upper limit plutonium solubility of 10 -5 M in high pH and a conservative distribution coefficient for organic extractants of a 0 for plutonium in 30% TBP at 0.07 M HNO 3 ), the estimated concentration for plutonium in the organic phase would be -7 M. This is well below the process control criteria. A significant increase in plutonium solubility or the E a o would have to occur to raise this concentration to the 0.01 M concern level for organics. Measured tank chemical component values, expected operating conditions, and the characteristics of the expected chemistry and extraction mechanisms indicate that concentration of plutonium from Hanford tank residual sludges to associated process organic extractants is significantly below levels of concern

Dynamic process model of a plutonium oxalate precipitator

International Nuclear Information System (INIS)

Borgonovi, G.M.; Hammelman, J.E.; Miller, C.L.

1980-01-01

A dynamic model of a plutonium oxalate precipitator is developed to provide a means of predicting plutonium inventory on a continuous basis. The model is based on state-of-the-art crystallization equations, which describe nucleation and growth phenomena. The model parameters were obtained through the use of batch experimental data. The model has been used to study the approach to steady state, to investigate the response to input transients, and to simulate the control of the precipitation process. 12 refs

Precipitation of plutonium (III) oxalate and calcination to plutonium oxide

International Nuclear Information System (INIS)

Esteban, A.; Orosco, E.H.; Cassaniti, P.; Greco, L.; Adelfang, P.

1989-01-01

The plutonium based fuel fabrication requires the conversion of the plutonium nitrate solution from nuclear fuel reprocessing into pure PuO2. The conversion method based on the precipitation of plutonium (III) oxalate and subsequent calcination has been studied in detail. In this procedure, plutonium (III) oxalate is precipitated, at room temperature, by the slow addition of 1M oxalic acid to the feed solution, containing from 5-100 g/l of plutonium in 1M nitric acid. Before precipitation, the plutonium is adjusted to trivalent state by addition of 1M ascorbic acid in the presence of an oxidation inhibitor such as hydrazine. Finally, the precipitate is calcinated at 700 deg C to obtain PuO2. A flowsheet is proposed in this paper including: a) A study about the conditions to adjust the plutonium valence. b) Solubility data of plutonium (III) oxalate and measurements of plutonium losses to the filtrate and wash solution. c) Characterization of the obtained products. Plutonium (III) oxalate has several potential advantages over similar conversion processes. These include: 1) Formation of small particle sizes powder with good pellets fabrication characteristics. 2) The process is rather insensitive to most process variables, except nitric acid concentration. 3) Ambient temperature operations. 4) The losses of plutonium to the filtrate are less than in other conversion processes. (Author) [es

Development of an expert system for analysis of plutonium processing operations

International Nuclear Information System (INIS)

Boeringter, S.T.; Fasel, J.H.; Kornreich, D.E.

2001-01-01

At Los Alamos National Laboratory (LANL) an expert system has been developed for the analysis and assessment of plutonium processing operations. This system is based upon an object-oriented simulation environment specifically developed for the needs of nuclear material processing. The simulation environment, called the ''Process Modeling System'' (ProMoS), contains a library of over 250 plutonium-based unit process operations ranging from analytical chemistry, oxide operations, recycle and recovery, waste management, and component fabrication. (author)

The use of safeguards data for process monitoring in the Advanced Test Line for Actinide Separations

International Nuclear Information System (INIS)

Barnes, J.W.; Yarbro, S.L.

1987-01-01

Los Alamos is constructing an integrated process monitoring/materials control and accounting (PM/MC and A) system in the Advanced Testing Line for Actinide Separations (ATLAS) at the Los Alamos Plutonium Facility. The ATLAS will test and demonstrate new methods for aqueous processing of plutonium. The ATLAS will also develop, test, and demonstrate the concepts for integrated process monitoring/materials control and accounting. We describe how this integrated PM/MC and A system will function and provide benefits to both process research and materials accounting personnel

Treatment of plutonium contaminated ashes by electrogenerated Ag(II): a new, simple and efficient process

International Nuclear Information System (INIS)

Madic, C.; Saulze, J.L.; Bourges, J.; Lecomte, M.; Koehly, G.

1990-01-01

Incineration is a very attractive technique for managing plutonium contaminated solid wastes, allowing for large volume and mass reduction factors. After waste incineration, the plutonium is concentrated in the ashes and an efficient method must be designed for its recovery. To achieve this goal, a process based on the dissolution of plutonium in nitric solution under the agressive action of electrogenerated Ag(II) was developed. This process is very simple, requiring very few steps. Plutonium recovery yields up to 98% can be obtained and, in addition, the plutonium bearing solutions generated by the treatment can be processed by the PUREX technique for plutonium recovery. This process constitutes the basis for the development of industrial facilities: 1) a pilot facility is being built in MARCOULE (COGEMA, UP1 plant), to treat active ash in 1990; 2) an industrial facility will be built in the MELOX plant under construction at MARCOULE (COGEMA plant)

The plutonium fuel cycles

International Nuclear Information System (INIS)

Pigford, T.H.; Ang, K.P.

1975-01-01

The quantities of plutonium and other fuel actinides have been calculated for equilibrium fuel cycles for 1000-MW water reactors fueled with slightly enriched uranium, water reactors fueled with plutonium and natural uranium, fast-breder reactors, gas-cooled reactors fueled with thorium and highly enriched uranium, and gas-cooled reactors fueled with thorium, plutonium and recycled uranium. The radioactivity quantities of plutonium, americium and curium processed yearly in these fuel cycles are greatest for the water reactors fueled with natural uranium and recycled plutonium. The total amount of actinides processed is calculated for the predicted future growth of the U.S. nuclear power industry. For the same total installed nuclear power capacity, the introduction of the plutonium breeder has little effect upon the total amount of plutonium in this century. The estimated amount of plutonium in the low-level process wastes in the plutonium fuel cycles is comparable to the amount of plutonium in the high-level fission product wastes. The amount of plutonium processed in the nuclear fuel cycles can be considerably reduced by using gas-cooled reactors to consume plutonium produced in uranium-fueled water reactors. These, and other reactors dedicated for plutonium utilization, could be co-located with facilities for fuel reprocessing ad fuel fabrication to eliminate the off-site transport of separated plutonium. (author)

Advanced concept of reduced-moderation water reactor (RMWR) for plutonium multiple recycling

International Nuclear Information System (INIS)

Okubo, T.; Iwamura, T.; Takeda, R.; Yamamoto, K.; Okada, H.

2001-01-01

An advanced water-cooled reactor concept named the Reduced-Moderation Water Reactor (RMWR) has been proposed to attain a high conversion ratio more than 1.0 and to achieve the negative void reactivity coefficient. At present, several types of design concepts satisfying both the design targets have been proposed based on the evaluation for the fuel without fission products and minor actinides. In this paper, the feasibility of the RMWR core is investigated for the plutonium multiple recycling under advanced reprocessing schemes with low decontamination factors as proposed for the FBR fuel cycle. (author)

Conversion of plutonium scrap and residue to boroilicate glass using the GMODS process

International Nuclear Information System (INIS)

Forsberg, C.W.; Beahm, E.C.; Parker, G.W.; Rudolph, J.; Elam, K.R.; Ferrada, J.J.

1995-01-01

Plutonium scrap and residue represent major national and international concerns because (1) significant environmental, safety, and health (ES ampersand H) problems have been identified with their storage; (2) all plutonium recovered from the black market in Europe has been from this category; (3) storage costs are high; and (4) safeguards are difficult. It is proposed to address these problems by conversion of plutonium scrap and residue to a CRACHIP (CRiticality, Aerosol, and CHemically Inert Plutonium) glass using the Glass Material Oxidation and Dissolution System (GMODS). CRACHIP refers to a set of requirements for plutonium storage forms that minimize ES ampersand H concerns. The concept is several decades old. Conversion of plutonium from complex chemical mixtures and variable geometries into a certified, qualified, homogeneous CRACHIP glass creates a stable chemical form that minimizes ES ampersand H risks, simplifies safeguards and security, provides an easy-to-store form, decreases storage costs, and allows for future disposition options. GMODS is a new process to directly convert metals, ceramics, and amorphous solids to glass; oxidize organics with the residue converted to glass; and convert chlorides to borosilicate glass and a secondary sodium chloride stream. Laboratory work has demonstrated the conversion of cerium (a plutonium surrogate), uranium (a plutonium surrogate), Zircaloy, stainless steel, and other materials to glass. GMODS is an enabling technology that creates new options. Conventional glassmaking processes require conversion of feeds to oxide-like forms before final conversion to glass. Such chemical conversion and separation processes are often complex and expensive

1981 Annual Status Report. Plutonium fuels and actinide programme

International Nuclear Information System (INIS)

1981-01-01

In this 1981 report the work carried out by the European Institute for Transuranium elements is reviewed. Main topics are: operation limits of plutonium fuels: swelling of advanced fuels, oxide fuel transients, equation of state of nuclear materials; actinide cycle safety: formation of actinides (FACT), safe handling of plutonium fuel (SHAPE), aspects of the head-end processing of carbide fuel (RECARB); actinide research: crystal chemistry, solid state studies, applied actinide research

Advanced Purex process for the new French reprocessing plants

International Nuclear Information System (INIS)

Viala, M.; Ledermann, P.; Pradel, P.

1993-01-01

The paper describes the main process innovations of the new Cogema reprocessing plants of La Hague (UP3 and UP2 800). Major improvements of process like the use of rotary dissolvers and annular columns, and also entirely new processes like solvent distillation and plutonium oxidizing dissolution, yield an advanced Purex process. The results of these innovations are significant improvements for throughput, end-products purification performances and waste minimization. They contribute also to limit personnel exposure. The main results of the first three years of operation are described. (author). 3 refs., 5 figs

Improving Efficiency with 3-D Imaging: Technology Essential in Removing Plutonium Processing Equipment from Plutonium Finishing Plant Gloveboxes

International Nuclear Information System (INIS)

Crow, Stephen H.; Kyle, Richard N.; Minette, Michael J.

2008-01-01

The Plutonium Finishing Plant at Hanford, Washington began operations in 1949 to process plutonium and plutonium products. Its primary mission was to produce plutonium metal, fabricate weapons parts, and stabilize reactive materials. These operations, and subsequent activities, were performed in remote production lines, consisting primarily of hundreds of gloveboxes. Over the years these gloveboxes and processes have been continuously modified. The plant is currently inactive and Fluor Hanford has been tasked to clean out contaminated equipment and gloveboxes from the facility so it can be demolished in the near future. Approximately 100 gloveboxes at PFP have been cleaned out in the past four years and about 90 gloveboxes remain to be cleaned out. Because specific commitment dates for this work have been established with the State of Washington and other entities, it is important to adopt work practices that increase the safety and speed of this effort. The most recent work practice to be adopted by Fluor Hanford D and D workers is the use of 3-D models to improve the efficiency of cleaning out radioactive gloveboxes at the plant. The use of 3-D models has significantly improved the work planning process by providing workers with a clear image of glovebox construction and composition, which is then used to determine cleanout methods and work sequences. The 3-D visual products enhance safety by enabling workers to more easily identify hazards and implement controls. In addition, the ability to identify and target the removal of radiological materials early in the D and D process provides substantial dose reduction for the workers

Some aspects of a technology of processing weapons grade plutonium to nuclear fuel

International Nuclear Information System (INIS)

Bibilashvili, Y.; Glagovsky, E.M.; Zakharkin, B.S.; Orlov, V.K.; Reshetnikov, F.G.; Rogozkin, B.G.; Soloni-N, M.I.

2000-01-01

The concept by Russia to use fissile weapons-grade materials, which are being recovered from nuclear pits in the process of disarmament, is based on an assessment of weapons-grade plutonium as an important energy source intended for use in nuclear power plants. However, in the path of involving plutonium excessive from the purposes of national safety into industrial power engineering there are a lot of problems, from which effectiveness and terms of its disposition are being dependent upon. Those problems have political, economical, financial and environmental character. This report outlines several technology problems of processing weapons-grade metallic plutonium into MOX-fuel for reactors based on thermal and fast neutrons, in particular, the issue of conversion of the metal into dioxide from the viewpoint of fabrication of pelletized MOX-fuel. The processing of metallic weapons-grade plutonium into nuclear fuel is a rather complicated and multi-stage process, every stage of which is its own production. Some of the stages are absent in production of MOX-fuel, for instance the stage of the conversion, i.e. transferring of metallic plutonium into dioxide of the ceramic quality. At this stage of plutonium utilization some tasks must be resolved as follows: I. As a result of the conversion, a material purified from ballast and radiogenic admixtures has to be obtained. This one will be applied to fabricate pelletized MOX-fuel going from morphological, physico-mechanical and technological properties. II. It is well known that metallic gallium, which is used as an alloying addition in weapons-grade plutonium, actively reacts with multiple metals. Therefore, an important issue is to study the effect of gallium on the technology of MOX-fuel production, quality of the pellets, as well as the interaction of gallium oxide with zirconium and steel shells of fuel elements depending upon the content of gallium in the fuel. The rate of the interaction of gallium oxide

Study of plutonium multi-recycle in high moderation LWR cores

International Nuclear Information System (INIS)

Iwata, Yutaka; Yamamoto, Toru; Ueji, Masao; Hibi, Koki; Aoyama, Motoo; Sakurada, Koichi

2000-01-01

Nuclear Power Engineering Corporation (NUPEC) has been studying advanced cores that are dedicated to enhance the plutonium consumption per recycling for effective use of plutonium. In this study, a fissile plutonium consumption rate is adopted as an index of the effective use of plutonium, which is defined as a ratio of consumption to loading of fissile plutonium in a core. High moderation core concepts have been studied in order to increase this index based on full MOX cores in the latest designs of LWRs in Japan that are the Advanced Boiling Water Reactor (ABWR) and the Advanced Pressurized Water Reactor (APWR). As a part of this study, core performance in the case of plutonium multi-recycling has been surveyed with these higher moderation cores aiming further effective use of plutonium. The design and analyses for equilibrium cores show that nuclear and thermal hydraulics parameters satisfy design criteria, and a fissile plutonium consumption rate increases up to 20% for ABWRs and 30% for APWRs even in plutonium multi-recycling condition. It was confirmed that the high moderation cores are feasible from a viewpoint of nuclear and thermal hydraulics, safety and plutonium consumption in the condition of plutonium multi-recycling. (author)

Decontamination of Battelle-Columbus' Plutonium Facility. Final report

International Nuclear Information System (INIS)

Rudolph, A.; Kirsch, G.; Toy, H.L.

1984-01-01

The Plutonium Laboratory, owned and operated by Battelle Memorial Institute's Columbus Division, was located in Battelle's Nuclear Sciences area near West Jefferson, Ohio, approximately 17 miles west of Columbus, Ohio. Originally built in 1960 for plutonium research and processing, the Plutonium Laboratory was enlarged in 1964 and again in 1967. With the termination of the Advanced Fuel Program in March, 1977, the decision was made to decommission the Plutonium Laboratory and to decontaminate the building for unrestricted use. Decontamination procedures began in January, 1978. All items which had come into contact with radioactivity from the plutonium operations were cleaned or disposed of through prescribed channels, maintaining procedures to ensure that D and D operations would pose no risk to the public, the environment, or the workers. The entire program was conducted under the cognizance of DOE's Chicago Operations Office. The building which housed the Plutonium Laboratory has now been decontaminated to levels allowing it to house ordinary laboratory and office operations. A ''Finding of No Significant Impact'' (FNSI) was issued in May, 1980

Method of processing plutonium and uranium solution

International Nuclear Information System (INIS)

Otsuka, Katsuyuki; Kondo, Isao; Suzuki, Toru.

1989-01-01

Solutions of plutonium nitrate solutions and uranyl nitrate recovered in the solvent extraction step in reprocessing plants and nuclear fuel production plants are applied with low temperature treatment by means of freeze-drying under vacuum into residues containing nitrates, which are denitrated under heating and calcined under reduction into powders. That is, since complicate processes of heating, concentration and dinitration conducted so far for the plutonium solution and uranyl solution are replaced with one step of freeze-drying under vacuum, the process can be simplified significantly. In addition, since the treatment is applied at low temperature, occurrence of corrosion for the material of evaporation, etc. can be prevented. Further, the number of operators can be saved by dividing the operations into recovery of solidification products, supply and sintering of the solutions and vacuum sublimation. Further, since nitrates processed at a low temperature are powderized by heating dinitration, the powderization step can be simplified. The specific surface area and the grain size distribution of the powder is made appropriate and it is possible to obtain oxide powders of physical property easily to be prepared into pellets. (N.H.)

A review of plutonium oxalate decomposition reactions and effects of decomposition temperature on the surface area of the plutonium dioxide product

International Nuclear Information System (INIS)

Orr, R.M.; Sims, H.E.; Taylor, R.J.

2015-01-01

Plutonium (IV) and (III) ions in nitric acid solution readily form insoluble precipitates with oxalic acid. The plutonium oxalates are then easily thermally decomposed to form plutonium dioxide powder. This simple process forms the basis of current industrial conversion or ‘finishing’ processes that are used in commercial scale reprocessing plants. It is also widely used in analytical or laboratory scale operations and for waste residues treatment. However, the mechanisms of the thermal decompositions in both air and inert atmospheres have been the subject of various studies over several decades. The nature of intermediate phases is of fundamental interest whilst understanding the evolution of gases at different temperatures is relevant to process control. The thermal decomposition is also used to control a number of powder properties of the PuO_2 product that are important to either long term storage or mixed oxide fuel manufacturing. These properties are the surface area, residual carbon impurities and adsorbed volatile species whereas the morphology and particle size distribution are functions of the precipitation process. Available data and experience regarding the thermal and radiation-induced decompositions of plutonium oxalate to oxide are reviewed. The mechanisms of the thermal decompositions are considered with a particular focus on the likely redox chemistry involved. Also, whilst it is well known that the surface area is dependent on calcination temperature, there is a wide variation in the published data and so new correlations have been derived. Better understanding of plutonium (III) and (IV) oxalate decompositions will assist the development of more proliferation resistant actinide co-conversion processes that are needed for advanced reprocessing in future closed nuclear fuel cycles. - Highlights: • Critical review of plutonium oxalate decomposition reactions. • New analysis of relationship between SSA and calcination temperature. • New SEM

An MCNP model of glove boxes in a plutonium processing facility

International Nuclear Information System (INIS)

Dooley, D.E.; Kornreich, D.E.

1998-01-01

Nuclear material processing usually occurs simultaneously in several glove boxes whose primary purpose is to contain radioactive materials and prevent inhalation or ingestion of radioactive materials by workers. A room in the plutonium facility at Los Alamos National Laboratory has been slated for installation of a glove box for storing plutonium metal in various shapes during processing. This storage glove box will be located in a room containing other glove boxes used daily by workers processing plutonium parts. An MCNP model of the room and glove boxes has been constructed to estimate the neutron flux at various locations in the room for two different locations of the storage glove box and to determine the effect of placing polyethylene shielding around the storage glove box. A neutron dose survey of the room with sources dispersed as during normal production operations was used as a benchmark to compare the neutron dose equivalent rates calculated by the MCNP model

An improved, computer-based, on-line gamma monitor for plutonium anion exchange process control

International Nuclear Information System (INIS)

Pope, N.G.; Marsh, S.F.

1987-06-01

An improved, low-cost, computer-based system has replaced a previously developed on-line gamma monitor. Both instruments continuously profile uranium, plutonium, and americium in the nitrate anion exchange process used to recover and purify plutonium at the Los Alamos Plutonium Facility. The latest system incorporates a personal computer that provides full-feature multichannel analyzer (MCA) capabilities by means of a single-slot, plug-in integrated circuit board. In addition to controlling all MCA functions, the computer program continuously corrects for gain shift and performs all other data processing functions. This Plutonium Recovery Operations Gamma Ray Energy Spectrometer System (PROGRESS) provides on-line process operational data essential for efficient operation. By identifying abnormal conditions in real time, it allows operators to take corrective actions promptly. The decision-making capability of the computer will be of increasing value as we implement automated process-control functions in the future. 4 refs., 6 figs

Adaptation of the IBM ECR [electric cantilever robot] robot to plutonium processing applications

International Nuclear Information System (INIS)

Armantrout, G.A.; Pedrotti, L.R.; Halter, E.A.; Crossfield, M.

1990-12-01

The changing regulatory climate in the US is adding increasing incentive to reduce operator dose and TRU waste for DOE plutonium processing operations. To help achieve that goal the authors have begun adapting a small commercial overhead gantry robot, the IBM electric cantilever robot (ECR), to plutonium processing applications. Steps are being taken to harden this robot to withstand the dry, often abrasive, environment within a plutonium glove box and to protect the electronic components against alpha radiation. A mock-up processing system for the reduction of the oxide to a metal was prepared and successfully demonstrated. Design of a working prototype is now underway using the results of this mock-up study. 7 figs., 4 tabs

Zirconolite glass-ceramics for plutonium immobilization: The effects of processing redox conditions on charge compensation and durability

Energy Technology Data Exchange (ETDEWEB)

Zhang, Yingjie, E-mail: yzx@ansto.gov.au; Gregg, Daniel J.; Kong, Linggen; Jovanovich, Miodrag; Triani, Gerry

2017-07-15

Zirconolite glass-ceramic samples doped with plutonium have been prepared via hot isostatic pressing. The effects of processing redox and plutonium loadings on plutonium valences, the presence of cation vacancies, zirconolite phase compositions, microstructures and durability have been investigated. Either tetravalent or trivalent plutonium ions may be incorporated on the Ca-site of CaZrTi{sub 2}O{sub 7} zirconolite with the Ca-site cation vacancies and the incorporation of Al{sup 3+} ions on the Ti-site for charge compensation. Plutonium and gadolinium (as a neutron absorber) are predominantly partitioned in zirconolite phases leading to the formation of chemically durable glass-ceramics suitable for the immobilization of impure plutonium wastes arising from the nuclear fuel cycle. - Highlights: •Plutonium validations of zirconolite glass-ceramics. •Effects of processing redox and plutonium loading. •Zirconolite phase compositions and plutonium valences. •Cation vacancies and chemical durability.

Uranium/plutonium and uranium/neptunium separation by the Purex process using hydroxyurea

International Nuclear Information System (INIS)

Zhu Zhaowu; He Jianyu; Zhang Zefu; Zhang Yu; Zhu Jianmin; Zhen Weifang

2004-01-01

Hydroxyurea dissolved in nitric acid can strip plutonium and neptunium from tri-butyl phosphate efficiently and has little influence on the uranium distribution between the two phases. Simulating the 1B contactor of the Purex process by hydroxyurea with nitric acid solution as a stripping agent, the separation factors of uranium/plutonium and uranium/neptunium can reach values as high as 4.7 x 10 4 and 260, respectively. This indicates that hydroxyurea is a promising salt free agent for uranium/plutonium and uranium/neptunium separations. (author)

Literature review for oxalate oxidation processes and plutonium oxalate solubility

Energy Technology Data Exchange (ETDEWEB)

Nash, C. A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2015-10-01

A literature review of oxalate oxidation processes finds that manganese(II)-catalyzed nitric acid oxidation of oxalate in precipitate filtrate is a viable and well-documented process. The process has been operated on the large scale at Savannah River in the past, including oxidation of 20 tons of oxalic acid in F-Canyon. Research data under a variety of conditions show the process to be robust. This process is recommended for oxalate destruction in H-Canyon in the upcoming program to produce feed for the MOX facility. Prevention of plutonium oxalate precipitation in filtrate can be achieved by concentrated nitric acid/ferric nitrate sequestration of oxalate. Organic complexants do not appear practical to sequester plutonium. Testing is proposed to confirm the literature and calculation findings of this review at projected operating conditions for the upcoming campaign.

Separation of americium and plutonium from nuclear wastes by the TRUEX process

International Nuclear Information System (INIS)

Leonard, R.A.; Vandegrift, G.F.; Manry, C.W.

1986-01-01

Americium and plutonium can be removed from a transuranic (TRU) waste stream to <10 nCi/g by the TRUEX process. The resulting waste is nontransuranic, greatly reducing disposal costs. An overview is given of the TRUEX process and of centrifugal contactors used to implement this process. Then, a plan for the deployment of TRUEX at the Hanford Site is discussed. Finally, details are given on the proposed use of TRUEX to treat the liquid wastes from the Plutonium Finishing Plant at the Hanford Site

A portable concentrator for processing plutonium containing solutions

International Nuclear Information System (INIS)

Chamberlain, D.B.; Conner, C.; Chen, L.

1995-01-01

This report describes a horizontal, compact agitated-film concentrator called a Rototherm, manufactured by Artisan Industries, Inc. which can be used to process aqueous solutions of radioactive wastes containing plutonium. The unit is designed to concentrate liquid streams to a high-solid content slurry

Stability with temperature of mixed uranium plutonium monocarbides

International Nuclear Information System (INIS)

Riglet-Martial, Ch.; Dumas, J.C.; Piron, J.P.; Gueneau, Ch.

2008-01-01

Full text: Among the different advanced fuel materials of concern for Generation IV systems, the mixed carbide of uranium and plutonium fuel is considered as one of the key materials for Gas Fast Reactors (GFR) systems. For purposes of optimising its fabrication process as well as its performances in various operating conditions, the losses of gaseous plutonium specially at elevated temperatures have to be controlled and minimized. The paper is therefore concerned with a parametric analysis of the stability with temperature of mixed carbides of uranium and plutonium. Previous published experimental studies have shown that mixed (U ,Pu) carbides undergo a highly incongruent sublimation at high temperatures: the vapour phase in equilibrium with the solid is mainly composed of gaseous plutonium (P Pu /P total > 99 % ) while the contribution of gaseous U and C remains very low. The composition of the system U 1-z Pu z C 1+x ' (z =Pu/(U+Pu) and x C/(U+Pu)), the temperature (T) and the expansion volume (V) of the gas are the main parameters in the loss of gaseous Pu. The calculations are carried out using the SAGE (Solgasmix Advanced Gibbs Energy) software, by assuming ideal solid solutions between UC and PuC, as well as between U 2 C 3 and Pu 2 C 3 . The validity of the model is previously tested using published equilibrium vapour pressure data. This work gives rise to a large description of the variations of Pu losses from mixed uranium plutonium carbides and leads to some basic recommendations in connection with the use of this advanced fuel materials

Some plutonium IV polymers properties in Purex process

International Nuclear Information System (INIS)

Scoazec, H.; Pasquiou, J.Y.; Germain, M.

1990-01-01

The metabolism of plutonium polymers in fuel reprocessing using the Purex process with tributylphosphate as solvent, and its practical consequence in real operation conditions are examined. Precipitation with dibutylphosphoric acid, a solvent degradation product, occurs both in extraction and stripping units when polymers are present. (author)

CSER 00-003: Criticality Safety Evaluation report for PFP Magnesium Hydroxide Precipitation Process for Plutonium Stabilization Glovebox 3

International Nuclear Information System (INIS)

LAN, J.S.

2000-01-01

This Criticality Safety Evaluation Report analyzes the stabilization of plutonium/uranium solutions in Glovebox 3 using the magnesium hydroxide precipitation process at PFP. The process covered are the receipt of diluted plutonium solutions into three precipitation tanks, the precipitation of plutonium from the solution, the filtering of the plutonium precipitate from the solution, the scraping of the precipitate from the filter into boats, and the initial drying of the precipitated slurry on a hot plate. A batch (up to 2.5 kg) is brought into the glovebox as plutonium nitrate, processed, and is then removed in boats for further processing. This CSER establishes limits for the magnesium hydroxide precipitation process in Glovebox 3 to maintain criticality safety while handling fissionable material

Applications of molten salts in plutonium processing

International Nuclear Information System (INIS)

Bowersox, D.F.; Christensen, D.C.; Williams, J.D.

1987-01-01

Plutonium is efficiently recovered from scrap at Los Alamos by a series of chemical reactions and separations conducted at temperatures ranging from 700 to 900 0 C. These processes usually employ a molten salt or salt eutectic as a heat sink and/or reaction medium. Salts for these operations were selected early in the development cycle. The selection criteria are being reevaluated. In this article we describe the processes now in use at Los Alamos and our studies of alternate salts and eutectics

Properties of plutonium

International Nuclear Information System (INIS)

Ahn, Jin Su; Yoon, Hwan Ki; Min, Kyung Sik; Kim, Hyun Tae; Ahn, Jong Sung; Kwag, Eon Ho; Ryu, Keon Joong

1996-03-01

Plutonium has unique chemical and physical properties. Its uniqueness in use has led to rare publications, in Korea. This report covers physical aspects of phase change of metal plutonium, mechanical properties, thermal conductivity, etc, chemical aspects of corrosion, oxidation, how to produce plutonium from spent fuels by describing various chemical treatment methods, which are currently used and were used in the past. It also contains characteristics of the purex reprocessing process which is the most widely used nowadays. And show processes to purify and metalize from recovered plutonium solution. Detection and analysis methods are introduced with key pints for handling, critical safety, toxicity, and effects on peoples. This report gives not only a general idea on what plutonium is, rather than deep technical description, but also basic knowledge on plutonium production and safeguards diversion from the view point of nonproliferation. 18 refs. (Author) .new

Properties of plutonium

Energy Technology Data Exchange (ETDEWEB)

Ahn, Jin Su; Yoon, Hwan Ki; Min, Kyung Sik; Kim, Hyun Tae; Ahn, Jong Sung; Kwag, Eon Ho; Ryu, Keon Joong [Korea Atomic Energy Research Institute, Daeduk (Korea, Republic of)

1996-03-01

Plutonium has unique chemical and physical properties. Its uniqueness in use has led to rare publications, in Korea. This report covers physical aspects of phase change of metal plutonium, mechanical properties, thermal conductivity, etc, chemical aspects of corrosion, oxidation, how to produce plutonium from spent fuels by describing various chemical treatment methods, which are currently used and were used in the past. It also contains characteristics of the purex reprocessing process which is the most widely used nowadays. And show processes to purify and metalize from recovered plutonium solution. Detection and analysis methods are introduced with key pints for handling, critical safety, toxicity, and effects on peoples. This report gives not only a general idea on what plutonium is, rather than deep technical description, but also basic knowledge on plutonium production and safeguards diversion from the view point of nonproliferation. 18 refs. (Author) .new.

Baseline process description for simulating plutonium oxide production for precalc project

Energy Technology Data Exchange (ETDEWEB)

Pike, J. A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2017-10-26

Savannah River National Laboratory (SRNL) started a multi-year project, the PreCalc Project, to develop a computational simulation of a plutonium oxide (PuO₂) production facility with the objective to study the fundamental relationships between morphological and physicochemical properties. This report provides a detailed baseline process description to be used by SRNL personnel and collaborators to facilitate the initial design and construction of the simulation. The PreCalc Project team selected the HB-Line Plutonium Finishing Facility as the basis for a nominal baseline process since the facility is operational and significant model validation data can be obtained. The process boundary as well as process and facility design details necessary for multi-scale, multi-physics models are provided.

CONTAMINATED PROCESS EQUIPMENT REMOVAL FOR THE DECOMMISSIONG AND DECONTAMINATION OF THE 232-Z CONTAMINATED WASTE RECOVERY PROCESS FACILITY AT THE PLUTONIUM FINISHING PLANT

International Nuclear Information System (INIS)

HOPKINS, A.M.; MINETTE, M.J.; KLOS, D.B.

2007-01-01

This paper describes the unique challenges encountered and subsequent resolutions to accomplish the deactivation and decontamination of a plutonium ash contaminated building. The 232-Z Contaminated Waste Recovery Process Facility at the Plutonium Finishing Plant was used to recover plutonium from process wastes such as rags, gloves, containers and other items by incinerating the items and dissolving the resulting ash. The incineration process resulted in a light-weight plutonium ash residue that was highly mobile in air. This light-weight ash coated the incinerator's process equipment, which included gloveboxes, blowers, filters, furnaces, ducts, and filter boxes. Significant airborne contamination (over 1 million derived air concentration hours [DAC]) was found in the scrubber cell of the facility. Over 1300 grams of plutonium held up in the process equipment and attached to the walls had to be removed, packaged and disposed. This ash had to be removed before demolition of the building could take place

Conversion of metal plutonium to plutonium dioxide by pyrochemical method

Energy Technology Data Exchange (ETDEWEB)

Panov, A.V.; Subbotin, V.G. [Russian Federal Nuclear Center, ALL-Russian Science and Research Institute of Technical Physics, Snezhinsk (Russian Federation); Mashirev, V.P. [ALL-Russian Science and Research Institute of Chemical Technology, Moscow (Russian Federation)

2000-07-01

Report contains experimental results on metal plutonium of weapon origin samples conversion to plutonium dioxide by pyrochemical method. Circuits of processes are described. Their advantages and shortcomings are shown. Parameters of plutonium dioxide powders (phase and fraction compositions, poured density) manufactured by pyrochemical method in RFNC-VNIITF are shown as well. (authors)

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

Energy Technology Data Exchange (ETDEWEB)

Lumetta, Gregg J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Meier, David E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Tingey, Joel M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Casella, Amanda J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Delegard, Calvin H. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Edwards, Matthew K. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Orton, Robert D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Rapko, Brian M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Smart, John E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2015-05-01

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

A review of plutonium oxalate decomposition reactions and effects of decomposition temperature on the surface area of the plutonium dioxide product

Energy Technology Data Exchange (ETDEWEB)

Orr, R.M.; Sims, H.E.; Taylor, R.J., E-mail: robin.j.taylor@nnl.co.uk

2015-10-15

Plutonium (IV) and (III) ions in nitric acid solution readily form insoluble precipitates with oxalic acid. The plutonium oxalates are then easily thermally decomposed to form plutonium dioxide powder. This simple process forms the basis of current industrial conversion or ‘finishing’ processes that are used in commercial scale reprocessing plants. It is also widely used in analytical or laboratory scale operations and for waste residues treatment. However, the mechanisms of the thermal decompositions in both air and inert atmospheres have been the subject of various studies over several decades. The nature of intermediate phases is of fundamental interest whilst understanding the evolution of gases at different temperatures is relevant to process control. The thermal decomposition is also used to control a number of powder properties of the PuO{sub 2} product that are important to either long term storage or mixed oxide fuel manufacturing. These properties are the surface area, residual carbon impurities and adsorbed volatile species whereas the morphology and particle size distribution are functions of the precipitation process. Available data and experience regarding the thermal and radiation-induced decompositions of plutonium oxalate to oxide are reviewed. The mechanisms of the thermal decompositions are considered with a particular focus on the likely redox chemistry involved. Also, whilst it is well known that the surface area is dependent on calcination temperature, there is a wide variation in the published data and so new correlations have been derived. Better understanding of plutonium (III) and (IV) oxalate decompositions will assist the development of more proliferation resistant actinide co-conversion processes that are needed for advanced reprocessing in future closed nuclear fuel cycles. - Highlights: • Critical review of plutonium oxalate decomposition reactions. • New analysis of relationship between SSA and calcination temperature. �

PRODUCTION OF PLUTONIUM METAL

Science.gov (United States)

Lyon, W.L.; Moore, R.H.

1961-01-17

A process is given for producing plutonium metal by the reduction of plutonium chloride, dissolved in alkali metal chloride plus or minus aluminum chloride, with magnesium or a magnesium-aluminum alloy at between 700 and 800 deg C and separating the plutonium or plutonium-aluminum alloy formed from the salt.

Processing plutonium-contaminated soil on Johnston Atoll

International Nuclear Information System (INIS)

Moroney, K.; Moroney, J. III; Turney, J.

1994-01-01

This article describes a cleanup project to process plutonium- and americium-contaminated soil on Johnston Atoll for volume reduction. Thermo Analytical's (TMA's) segmented gate system (SGS) for this remedial operation has been in successful on-site operation since 1992. Topics covered include the basis for development, a description of the Johnston Atoll; the significance of results; the benefits of the technology; applicability to other radiologically contaminated sites. 7 figs., 1 tab

A review of plutonium oxalate decomposition reactions and effects of decomposition temperature on the surface area of the plutonium dioxide product

Science.gov (United States)

Orr, R. M.; Sims, H. E.; Taylor, R. J.

2015-10-01

Plutonium (IV) and (III) ions in nitric acid solution readily form insoluble precipitates with oxalic acid. The plutonium oxalates are then easily thermally decomposed to form plutonium dioxide powder. This simple process forms the basis of current industrial conversion or 'finishing' processes that are used in commercial scale reprocessing plants. It is also widely used in analytical or laboratory scale operations and for waste residues treatment. However, the mechanisms of the thermal decompositions in both air and inert atmospheres have been the subject of various studies over several decades. The nature of intermediate phases is of fundamental interest whilst understanding the evolution of gases at different temperatures is relevant to process control. The thermal decomposition is also used to control a number of powder properties of the PuO2 product that are important to either long term storage or mixed oxide fuel manufacturing. These properties are the surface area, residual carbon impurities and adsorbed volatile species whereas the morphology and particle size distribution are functions of the precipitation process. Available data and experience regarding the thermal and radiation-induced decompositions of plutonium oxalate to oxide are reviewed. The mechanisms of the thermal decompositions are considered with a particular focus on the likely redox chemistry involved. Also, whilst it is well known that the surface area is dependent on calcination temperature, there is a wide variation in the published data and so new correlations have been derived. Better understanding of plutonium (III) and (IV) oxalate decompositions will assist the development of more proliferation resistant actinide co-conversion processes that are needed for advanced reprocessing in future closed nuclear fuel cycles.

An environmentally benign plutonium processing future at Los Alamos

International Nuclear Information System (INIS)

Pillay, K.K.S.

1993-01-01

In recent years, the U.S. Department of Energy (DOE) has elevated environmental restoration and waste management to major mission areas, and it has established the reduction of wastes from DOE facilities as a major objective. The DOE facilities must now comply with all environmental regulations, including special regulations required of federal facilities. In recognition of this shift in philosophy, the plutonium processing facility at Los Alamos National Laboratory (LANL) has adopted the goal of becoming a facility that processes plutonium in a way that produces only environmentally benign waste. Becoming a facility with zero radionuclide and mixed-waste discharge is an extremely challenging goal and one that requires the technical contributions of a multidisciplinary team of experts. While all the technologies necessary to achieve this goal are not yet available, an extensive knowledge base does exist that can be applied to solving the remaining problems. Working toward this goal is a worthwhile endeavor, not only for LANL, but for the nuclear complex of the future

Six-kilogram-scale electrorefining of plutonium metal

International Nuclear Information System (INIS)

Mullins, L.J.; Morgan, A.N.; Apgar, S.A. III; Christensen, D.C.

1982-09-01

The electrorefining of metallic plutonium scrap to produce high purity metal has been an established procedure at Los Alamos since 1964. This is a batch process and was limited to 4-kg plutonium because of criticality safety considerations. Improvements in critical mass measurements have permitted us to develop a process for 6-kg plutonium. The 6-kg process is now operational. The increased size of the process, together with other improvements which have been made, makes plutonium electrorefining the principal industrial tool for processing and purifying metallic plutonium scrap

An Improved Plutonium Trifluoride Precipitation Flowsheet

Energy Technology Data Exchange (ETDEWEB)

Harmon, H.D.

2001-06-26

This report discusses results of the plutonium trifluoride two-stage precipitation study. A series of precipitation experiments was used to identify the significant process variables affecting precipitation performance. A mathematical model of the precipitation process was developed which is based on the formation of plutonium fluoride complexes. The precipitation model relates all process variables, in a single equation, to a single parameter which can be used to control the performance of the plutonium trifluoride precipitation process. Recommendations have been made which will optimize the FB-Line plutonium trifluoride precipitation process.

An Improved Plutonium Trifluoride Precipitation Flowsheet

International Nuclear Information System (INIS)

Harmon, H.D.

2001-01-01

This report discusses results of the plutonium trifluoride two-stage precipitation study. A series of precipitation experiments was used to identify the significant process variables affecting precipitation performance. A mathematical model of the precipitation process was developed which is based on the formation of plutonium fluoride complexes. The precipitation model relates all process variables, in a single equation, to a single parameter which can be used to control the performance of the plutonium trifluoride precipitation process. Recommendations have been made which will optimize the FB-Line plutonium trifluoride precipitation process

Plutonium scrap waste processing based on aqueous nitrate and chloride media

International Nuclear Information System (INIS)

Navratil, J.D.

1985-01-01

A brief review of plutonium scrap aqueous waste processing technology at Rocky Flats is given. Nitric acid unit operations include dissolution and leaching, anion exchange purification and precipitation. Chloride waste processing consists of cation exchange and carbonate precipitation. Ferrite and carrier precipitation waste treatment processes are also described. 3 figs

Plutonium Plant, Trombay

International Nuclear Information System (INIS)

Yadav, J.S.; Agarwal, K.

2017-01-01

The journey of Indian nuclear fuel reprocessing started with the commissioning of Plutonium Plant (PP) at Trombay on 22"n"d January, 1965 with an aim to reprocess the spent fuel from research reactor CIRUS. The basic process chosen for the plant was Plutonium Uranium Reduction EXtraction (PUREX) process. In seventies, the plant was subjected to major design modifications and replacement of hardware, which later met the additional demand from research reactor DHRUVA. The augmented plutonium plant has been operating since 1983. Experience gained from this plant was very much helpful to design future reprocessing plant in the country

Plutonium fires; Incendies de plutonium

Energy Technology Data Exchange (ETDEWEB)

Mestre, E.

1959-06-23

The author reports an information survey on accidents which occurred when handling plutonium. He first addresses accidents reported in documents. He indicates the circumstances and consequences of these accidents (explosion in glove boxes, fires of plutonium chips, plutonium fire followed by filter destruction, explosion during plutonium chip dissolution followed by chip fire). He describes hazards associated with plutonium fires: atmosphere and surface contamination, criticality. The author gives some advices to avoid plutonium fires. These advices concern electric installations, the use of flammable solvents, general cautions associated with plutonium handling, venting and filtration. He finally describes how to fight plutonium fires, and measures to be taken after the fire (staff contamination control, atmosphere control)

Drop-in capsule testing of plutonium-based fuels in the Advanced Test Reactor

International Nuclear Information System (INIS)

Chang, G.S.; Ryskamp, J.M.; Terry, W.K.; Ambrosek, R.G.; Palmer, A.J.; Roesener, R.A.

1996-09-01

The most attractive way to dispose of weapons-grade plutonium (WGPu) is to use it as fuel in existing light water reactors (LWRs) in the form of mixed oxide (MOX) fuel - i.e., plutonia (PuO[sub 2]) mixed with urania (UO[sub 2]). Before U.S. reactors could be used for this purpose, their operating licenses would have to be amended. Numerous technical issues must be resolved before LWR operating licenses can be amended to allow the use of MOX fuel. The proposed weapons-grade MOX fuel is unusual, even relative to ongoing foreign experience with reactor-grade MOX power reactor fuel. Some demonstration of the in- reactor thermal, mechanical, and fission gas release behavior of the prototype fuel will most likely be required in a limited number of test reactor irradiations. The application to license operation with MOX fuel must be amply supported by experimental data. The Advanced Test Reactor (ATR) at the Idaho National Engineering Laboratory (INEL) is capable of playing a key role in the irradiation, development, and licensing of these new fuel types. The ATR is a 250- MW (thermal) LWR designed to study the effects of intense radiation on reactor fuels and materials. For 25 years, the primary role of the ATR has been to serve in experimental investigations for the development of advanced nuclear fuels. Both large- and small-volume test positions in the ATR could be used for MOX fuel irradiation. The ATR would be a nearly ideal test bed for developing data needed to support applications to license LWRs for operation with MOX fuel made from weapons-grade plutonium. Furthermore, these data can be obtained more quickly by using ATR instead of testing in a commercial LWR. Our previous work in this area has demonstrated that it is technically feasible to perform MOX fuel testing in the ATR. This report documents our analyses of sealed drop-in capsules containing plutonium-based test specimens placed in various ATR positions

Continuous Material Balance Reconciliation for a Modern Plutonium Processing Facility

International Nuclear Information System (INIS)

CLARK, THOMASG.

2004-01-01

This paper describes a safeguards approach that can be deployed at any modern plutonium processing facility to increase the level of safeguards assurance and significantly reduce the impact of safeguards on process operations. One of the most perplexing problems facing the designers of plutonium processing facilities is the constraint placed upon the limit of error of the inventory difference (LEID). The current DOE manual constrains the LEID for Category I and II material balance areas to 2 per cent of active inventory up to a Category II quantity of the material being processed. For 239Pu a Category II quantity is two kilograms. Due to the large material throughput anticipated for some of the modern plutonium facilities, the required LEID cannot be achieved reliably during a nominal two month inventory period, even by using state-of-the-science non-destructive assay (NDA) methods. The most cost-effective and least disruptive solution appears to be increasing the frequency of material balance closure and thus reducing the throughput being measured during each inventory period. Current inventory accounting practices and systems can already provide the book inventory values at any point in time. However, closing the material balance with measured values has typically required the process to be cleaned out, and in-process materials packaged and measured. This process requires one to two weeks of facility down time every two months for each inventory, thus significantly reducing productivity. To provide a solution to this problem, a non-traditional approach is proposed that will include using in-line instruments to provide measurement of the process materials on a near real-time basis. A new software component will be developed that will operate with the standard LANMAS application to provide the running material balance reconciliation, including the calculation of the inventory difference and variance propagation. The combined measurement system and software

Plutonium storage phenomenology

International Nuclear Information System (INIS)

Szempruch, R.

1995-12-01

Plutonium has been produced, handled, and stored at Department of Energy (DOE) facilities since the 1940s. Many changes have occurred during the last 40 years in the sources, production demands, and end uses of plutonium. These have resulted in corresponding changes in the isotopic composition as well as the chemical and physical forms of the processed and stored plutonium. Thousands of ordinary food pack tin cans have been used successfully for many years to handle and store plutonium. Other containers have been used with equal success. This paper addressees the exceptions to this satisfactory experience. To aid in understanding the challenges of handling plutonium for storage or immobilization the lessons learned from past storage experience and the necessary countermeasures to improve storage performance are discussed

Treatment of plutonium process residues by molten salt oxidation

Energy Technology Data Exchange (ETDEWEB)

Stimmel, J.; Wishau, R.; Ramsey, K.B.; Montoya, A.; Brock, J. [Los Alamos National Lab., NM (United States); Heslop, M. [Naval Surface Warfare Center (United States). Indian Head Div.; Wernly, K. [Molten Salt Oxidation Corp. (United States)

1999-04-01

Molten Salt Oxidation (MSO) is a thermal process that can remove more than 99.999% of the organic matrix from combustible {sup 238}Pu material. Plutonium processing residues are injected into a molten salt bed with an excess of air. The salt (sodium carbonate) functions as a catalyst for the conversion of the organic material to carbon dioxide and water. Reactive species such as fluorine, chlorine, bromine, iodine, sulfur, phosphorous and arsenic in the organic waste react with the molten salt to form the corresponding neutralized salts, NaF, NaCl, NaBr, NaI, Na{sub 2}SO{sub 4}, Na{sub 3}PO{sub 4} and NaAsO{sub 2} or Na{sub 3}AsO4. Plutonium and other metals react with the molten salt and air to form metal salts or oxides. Saturated salt will be recycled and aqueous chemical separation will be used to recover the {sup 238}Pu. The Los Alamos National Laboratory system, which is currently in the conceptual design stage, will be scaled down from current systems for use inside a glovebox.

Treatment of plutonium process residues by molten salt oxidation

International Nuclear Information System (INIS)

Stimmel, J.; Wishau, R.; Ramsey, K.B.; Montoya, A.; Brock, J.; Heslop, M.

1999-01-01

Molten Salt Oxidation (MSO) is a thermal process that can remove more than 99.999% of the organic matrix from combustible 238 Pu material. Plutonium processing residues are injected into a molten salt bed with an excess of air. The salt (sodium carbonate) functions as a catalyst for the conversion of the organic material to carbon dioxide and water. Reactive species such as fluorine, chlorine, bromine, iodine, sulfur, phosphorous and arsenic in the organic waste react with the molten salt to form the corresponding neutralized salts, NaF, NaCl, NaBr, NaI, Na 2 SO 4 , Na 3 PO 4 and NaAsO 2 or Na 3 AsO4. Plutonium and other metals react with the molten salt and air to form metal salts or oxides. Saturated salt will be recycled and aqueous chemical separation will be used to recover the 238 Pu. The Los Alamos National Laboratory system, which is currently in the conceptual design stage, will be scaled down from current systems for use inside a glovebox

Stop plutonium; Stop plutonium

Energy Technology Data Exchange (ETDEWEB)

NONE

2003-02-01

This press document aims to inform the public on the hazards bound to the plutonium exploitation in France and especially the plutonium transport. The first part is a technical presentation of the plutonium and the MOX (Mixed Oxide Fuel). The second part presents the installation of the plutonium industry in France. The third part is devoted to the plutonium convoys safety. The highlight is done on the problem of the leak of ''secret'' of such transports. (A.L.B.)

Reduction of worldwide plutonium inventories using conventional reactors and advanced fuels: A systems study

International Nuclear Information System (INIS)

Krakowski, R.A.; Bathke, C.G.; Chodak, P. III

1997-01-01

The potential for reducing plutonium inventories in the civilian nuclear fuel cycle through recycle in LWRs of a variety of mixed-oxide forms is examined by means of a cost-based plutonium-flow systems model that includes an approximate measure of proliferation risk. The impact of plutonium recycle in a number of forms is examined, including the introduction of nonfertile fuels into conventional (LWR) reactors to reduce net plutonium generation, to increase plutonium burnup, and to reduce exo-reactor plutonium inventories

Process control and safeguards system plutonium inventory conrol for MOX fuel facility

International Nuclear Information System (INIS)

Mishima, T.; Aoki, M.; Muto, T.; Amanuma, T.

1979-01-01

The plutonium inventory control (PINC) system is a real-time material accountability control system that is expected to be applied to a new large-scale plutonium fuel production facility for both fast breeder reactor and heavy water reactor at the Power Reactor and Nuclear Development Corporation. The PINC is basically a system for material control but is expected to develop into a whole facility control system, including criticality control, process control, quality control, facility protection, and so forth. Under PINC, every process and storage area is divided into a unit area, which is the smallest unit for both accountability and process control. Item and material weight automatically are accounted for at every unit area, and data are simultaneously treated by a computer network system. Sensors necessary for the system are being developed. 9 figures

Post-remedial-action radiological survey of the Westinghouse Advanced Reactors Division Plutonium Fuel Laboratories, Cheswick, Pennsylvania, October 1-8, 1981

International Nuclear Information System (INIS)

Flynn, K.F.; Justus, A.L.; Sholeen, C.M.; Smith, W.H.; Wynveen, R.A.

1984-01-01

The post-remedial-action radiological assessment conducted by the ANL Radiological Survey Group in October 1981, following decommissioning and decontamination efforts by Westinghouse personnel, indicated that except for the Advanced Fuels Laboratory exhaust ductwork and north wall, the interior surfaces of the Plutonium Laboratory and associated areas within Building 7 and the Advanced Fuels Laboratory within Building 8 were below both the ANSI Draft Standard N13.12 and NRC Guideline criteria for acceptable surface contamination levels. Hence, with the exceptions noted above, the interior surfaces of those areas within Buildings 7 and 8 that were included in the assessment are suitable for unrestricted use. Air samples collected at the involved areas within Buildings 7 and 8 indicated that the radon, thoron, and progeny concentrations within the air were well below the limits prescribed by the US Surgeon General, the Environmental Protection Agency, and the Department of Energy. The Building 7 drain lines are contaminated with uranium, plutonium, and americium. Radiochemical analysis of water and dirt/sludge samples collected from accessible Low-Bay, High-Bay, Shower Room, and Sodium laboratory drains revealed uranium, plutonium, and americium contaminants. The Building 7 drain lines hence are unsuitable for release for unrestricted use in their present condition. Low levels of enriched uranium, plutonium, and americium were detected in an environmental soil coring near Building 8, indicating release or spillage due to Advanced Reactors Division activities or Nuclear Fuel Division activities undr NRC licensure. 60 Co contamination was detected within the Building 7 Shower Room and in soil corings from the environs of Building 7. All other radionuclide concentrations measured in soil corings and the storm sewer outfall sample collected from the environs about Buildings 7 and 8 were within the range of normally expected background concentrations

Study of an automatic dosing of neptunium in the industrial process of separation neptunium 237-plutonium 238

International Nuclear Information System (INIS)

Ros, Pierre

1973-01-01

The objective is to study and to adapt a method of automatic dosing of neptunium to the industrial process of separation and purification of plutonium 238, while taking the information quality and economic aspects into account. After a recall of some generalities on the production of plutonium 238, and the process of separation plutonium-neptunium, the author addresses the dosing of neptunium. The adopted measurement technique is spectrophotometry (of neptunium, of neptunium peroxide) which is the most flexible and economic to adapt to automatic control. The author proposes a project of chemical automatic machine, and discusses the complex (stoichiometry, form) and some aspects of neptunium dosing (redox reactions, process control) [fr

Advanced spent fuel processing technologies for the United States GNEP programme

International Nuclear Information System (INIS)

Laidler, J.J.

2007-01-01

Spent fuel processing technologies for future advanced nuclear fuel cycles are being developed under the scope of the Global Nuclear Energy Partnership (GNEP). This effort seeks to make available for future deployment a fissile material recycling system that does not involve the separation of pure plutonium from spent fuel. In the nuclear system proposed by the United States under the GNEP initiative, light water reactor spent fuel is treated by means of a solvent extraction process that involves a group extraction of transuranic elements. The recovered transuranics are recycled as fuel material for advanced burner reactors, which can lead in the long term to fast reactors with conversion ratios greater than unity, helping to assure the sustainability of nuclear power systems. Both aqueous and pyrochemical methods are being considered for fast reactor spent fuel processing in the current US development programme. (author)

Decontaminaion of metals containing plutonium and americium

International Nuclear Information System (INIS)

Seitz, M.G.; Gerding, T.J.; Steindler, M.J.

1979-06-01

Melt-slagging (melt-refining) techniques were evaluated as a decontamination and consolidation step for metals contaminated with oxides of plutonium and americium. Experiments were performed in which mild steel, stainless steel, and nickel contaminated with oxides of plutonium and americium were melted in the presence of silicate slags of various compositions. The metal products were low in contamination, with the plutonium and americium strongly fractionated to the slags. Partition coefficients (plutonium in slag/plutonium in steel) of 7 x 10 6 were measured with boro-silicate slag and of 3 x 10 6 with calcium, magnesium silicate slag. Decontamination of metals containing as much as 14,000 ppM plutonium appears to be as efficient as for metals with plutonium levels of 400 ppM. Staged extraction, that is, a remelting of processed metal with clean slag, results in further decontamination of the metal. The second extraction is effective with either resistance-furnace melting or electric-arc melting. Slag adhering to the metal ingots and in defects within the ingots is in the important contributors to plutonium retained in processed metals. If these sources of plutonium are controlled, the melt-refining process can be used on a large scale to convert highly contaminated metals to homogeneous and compact forms with very low concentrations of plutonium and americium. A conceptual design of a melt-refining process to decontaminate plutonium- and americium-contaminated metals is described. The process includes single-stage refining of contaminated metals to produce a metal product which would have less than 10 nCi/g of TRU-element contamination. Two plant sizes were considered. The smaller conceptual plant processes 77 kg of metal per 8-h period and may be portable.The larger one processes 140 kg of metal per 8-h period, is stationary, and may be near te maximum size that is practical for a metal decontamination process

Continuous plutonium(IV) oxalate precipitation, filtration, and calcination process. [From product streams from Redox, Purex, or Recuplex solvent extraction plants

Energy Technology Data Exchange (ETDEWEB)

Beede, R L

1956-09-27

A continuous plutonium (IV) oxalate precipitation, filtration, and calcination process has been developed. Continuous and batch decomposition of the oxalate in the filtrates has been demonstrated. The processes have been demonstrated in prototype equipment. Plutonium (IV) oxalate was precipitated continuously at room temperature by the concurrent addition of plutonium (IV) nitrate feed and oxalic acid into the pan of a modified rotary drum filter. The plutonium (IV) oxalate was calcined to plutonium dioxide, which could be readily hydrofluorinated. Continuous decomposition of the oxalate in synthetic plutonium (IV) oxalate filtrates containing plutonium (IV) oxalate solids was demonstrated using co-current flow in a U-shaped reactor. Feeds containing from 10 to 100 g/1 Pu, as plutonium (IV) nitrate, and 1.0 to 6.5 M HNO/sub 3/, respectively, can be processed. One molar oxalic acid is used as the precipitant. Temperatures of 20 to 35/sup 0/C for the precipitation and filtration are satisfactory. Plutonium (IV) oxalate can be calcined at 300 to 400/sup 0/C in a screw-type drier-calciner to plutonium dioxide and hydrofluorinated at 450 to 550/sup 0/C. Plutonium dioxide exceeding purity requirements has been produced in the prototype equipment. Advantages of continuous precipitation and filtration are: uniform plutonium (IV) oxalate, improved filtration characteristics, elimination of heating and cooling facilities, and higher capacities through a single unit. Advantages of the screw-type drier-calciner are the continuous production of an oxide satisfactory for feed for the proposed plant vibrating tube hydrofluorinator, and ease of coupling continuous precipitation and filtration to this proposed hydrofluorinator. Continuous decomposition of oxalate in filtrates offers advantages in decreasing filtrate storage requirements when coupled to a filtrate concentrator. (JGB)

Hold-up monitoring system for plutonium process tanks

International Nuclear Information System (INIS)

Zhu Rongbao; Jin Huimin; Tan Yajun

1994-01-01

The development of hold-up monitoring system for plutonium process tanks and a calculation method for α activities deposited in containers and inner walls of pipe are described. The hardware of monitoring system consists of a portable HPGe detector, a φ50 mm x 60 mm NaI(Tl) detector, γ-ray tungsten collimators, ORTEC92X Spectrum Master and an AST-286 computer. The software of system includes Maestro Tm for Window3 and a PHOUP1 hold-up application software for user. The Monte-Carlo simulation calculation supported by MCNP software is performed for the probability calculation of all the unscattering γ-rays reaching to the detection positions from the source terms deposited in the complicated tanks. A measurement mean value for different positions is used to minimize the effect of heterogeneous distribution of source term. The sensitivity is better than 3.7 x 10 6 Bq/kg (steel) for a plutonium simulation source on a 3-8 mm thick steel plate surrounded by 0.8 x 10 -10 C/kg·s γ field from long-life fission products

Production of Plutonium Metal from Aqueous Solutions

Energy Technology Data Exchange (ETDEWEB)

Orth, D.A.

2003-01-16

The primary separation of plutonium from irradiated uranium by the Purex solvent extraction process at the Savannah River Plant produces a dilute plutonium solution containing residual fission products and uranium. A cation exchange process is used for concentration and further decontamination of the plutonium, as the first step in the final preparation of metal. This paper discusses the production of plutonium metal from the aqueous solutions.

Preliminary process simulation and analysis of GMODS: Processing of plutonium surplus materials

International Nuclear Information System (INIS)

Ferrada, J.J.; Nehls, J.W. Jr.; Welch, T.D.; Giardina, J.L.; Forsberg, C.W.; Maliyekkel, A.T.

1996-01-01

To address growing concerns in the areas of arms control, control of fissile materials, waste management, and environment and health, the US Department of Energy is studying and evaluating various options for the control and disposal of surplus fissile materials (SFMs). One of the options under consideration is the Glass Material Oxidation and Dissolution System (GMODS) which directly converts plutonium-bearing materials such as metals, ceramics, and organics into a durable-high-quality glass for long-term storage or a waste form for disposal. This study undertook the development of a computer simulation of the GMODS process using FLOW. That computer simulation was used to perform an assessment of how GMODS would handle the treatment of plutonium, rich scrap (RS) and lead scrap (LS), and identify critical process parameters. Among the key process parameters affecting the glass formation were processing temperatures, additives, and the effects of varying them on the final product. This assessment looked at the quantity of glass produced, the quality of the final glass form, and the effect of blending different groups of the feed streams on the glass produced. The model also provided a way to study the current process assumptions and determine in which areas more experimental studies are required. The simulation showed that the glass chemistry postulated in the models is workable. It is expected that the glass chemistry assumed during the modeling process can be verified by the results of the laboratory experiments that are currently being conducted relating to the GMODS process.Further waste characterization, especially of the SFM waste streams not studied in this report, will provide more nearly accurate results and give a more detailed evaluation of the GMODS process

Preliminary process simulation and analysis of GMODS: Processing of plutonium surplus materials

Energy Technology Data Exchange (ETDEWEB)

Ferrada, J.J.; Nehls, J.W. Jr.; Welch, T.D.; Giardina, J.L.; Forsberg, C.W. [Oak Ridge National Lab., TN (United States); Maliyekkel, A.T. [Oak Ridge Associated Universities, TN (United States)

1996-01-02

To address growing concerns in the areas of arms control, control of fissile materials, waste management, and environment and health, the US Department of Energy is studying and evaluating various options for the control and disposal of surplus fissile materials (SFMs). One of the options under consideration is the Glass Material Oxidation and Dissolution System (GMODS) which directly converts plutonium-bearing materials such as metals, ceramics, and organics into a durable-high-quality glass for long-term storage or a waste form for disposal. This study undertook the development of a computer simulation of the GMODS process using FLOW. That computer simulation was used to perform an assessment of how GMODS would handle the treatment of plutonium, rich scrap (RS) and lead scrap (LS), and identify critical process parameters. Among the key process parameters affecting the glass formation were processing temperatures, additives, and the effects of varying them on the final product. This assessment looked at the quantity of glass produced, the quality of the final glass form, and the effect of blending different groups of the feed streams on the glass produced. The model also provided a way to study the current process assumptions and determine in which areas more experimental studies are required. The simulation showed that the glass chemistry postulated in the models is workable. It is expected that the glass chemistry assumed during the modeling process can be verified by the results of the laboratory experiments that are currently being conducted relating to the GMODS process.Further waste characterization, especially of the SFM waste streams not studied in this report, will provide more nearly accurate results and give a more detailed evaluation of the GMODS process.

Design-Only Conceptual Design Report: Plutonium Immobilization Plant

International Nuclear Information System (INIS)

DiSabatino, A.; Loftus, D.

1999-01-01

This design-only conceptual design report was prepared to support a funding request by the Department of Energy Office of Fissile Materials Disposition for engineering and design of the Plutonium Immobilization Plant, which will be used to immobilize up to 50 tonnes of surplus plutonium. The siting for the Plutonium Immobilization Plant will be determined pursuant to the site-specific Surplus Plutonium Disposition Environmental Impact Statement in a Plutonium Deposition Record of Decision in early 1999. This document reflects a new facility using the preferred technology (ceramic immobilization using the can-in-canister approach) and the preferred site (at Savannah River). The Plutonium Immobilization Plant accepts plutonium from pit conversion and from non-pit sources and, through a ceramic immobilization process, converts the plutonium into mineral-like forms that are subsequently encapsulated within a large canister of high-level waste glass. The final immobilized product must make the plutonium as inherently unattractive and inaccessible for use in nuclear weapons as the plutonium in spent fuel from commercial reactors and must be suitable for geologic disposal. Plutonium immobilization at the Savannah River Site uses: (1) A new building, the Plutonium Immobilization Plant, which will convert non-pit surplus plutonium to an oxide form suitable for the immobilization process, immobilize plutonium in a titanate-based ceramic form, place cans of the plutonium-ceramic forms into magazines, and load the magazines into a canister; (2) The existing Defense Waste Processing Facility for the pouring of high-level waste glass into the canisters; and (3) The Actinide Packaging and Storage Facility to receive and store feed materials. The Plutonium Immobilization Plant uses existing Savannah River Site infra-structure for analytical laboratory services, waste handling, fire protection, training, and other support utilities and services. The Plutonium Immobilization Plant

Evaluation of TASTEX task H: measurement of plutonium isotopic abundances by gamma-ray spectrometry

International Nuclear Information System (INIS)

Gunnink, R.; Prindle, A.L.; Asakura, Y.; Masui, J.; Ishiguro, N.; Kawasaki, A.; Kataoka, S.

1981-10-01

This report describes a computer-based gamma spectrometer system that was developed for measuring isotopic and total plutonium concentrations in nitric acid solutions. The system was installed at the Tokai reprocessing plant where it is undergoing testing and evaluation as part of the Tokai Advanced Safeguards Exercise (TASTEX). Objectives of TASTEX Task H, High-Resolution Gamma Spectrometer for Plutonium Isotopic Analysis, the methods and equipment used, the installation and calibration of the system, and the measurements obtained from several reprocessing campaigns are discussed and described. In general, we find that measurements for gamma spectroscopy agree well with those of mass spectrometry and of other chemical analysis. The system measures both freshly processed plutonium from the product accountability tank and aged plutonium solutions from storage tanks. 14 figures, 15 tables

Determination of uranium and plutonium in metal conversion products from electrolytic reduction process

International Nuclear Information System (INIS)

Lee, Chang Heon; Suh, Moo Yul; Joe, Kih Soo; Sohn, Se Chul; Jee, Kwang Young; Kim, Won Ho

2005-01-01

Chemical characterization of process materials is required for the optimization of an electrolytic reduction process in which uranium dioxide, a matrix of spent PWR fuels, is electrolytically reduced to uranium metal in a medium of LiCl-Li 2 O molten at 650 .deg. C. A study on the determination of fissile materials in the uranium metal products containing corrosion products, fission products and residual process materials has been performed by controlled-potential coulometric titration which is well known in the field of nuclear science and technology. Interference of Fe, Ni, Cr and Mg (corrosion products), Nd (fission product) and LiCl molten salt (residual process material) on the determination of uranium and plutonium, and the necessity of plutonium separation prior to the titration are discussed in detail. Under the analytical condition established already, their recovery yields are evaluated along with analytical reliability

Glutarimidedioxime. A complexing and reducing reagent for plutonium recovery from spent nuclear fuel reprocessing

Energy Technology Data Exchange (ETDEWEB)

Xian, Liang [China Institute of Atomic Energy, Beijing (China). Radiochemistry Dept.; Tian, Guoxin [China Institute of Atomic Energy, Beijing (China). Radiochemistry Dept.; Lawrence Berkeley National Laboratory, Berkeley, CA (United States). Chemical Sciences Div.; Beavers, Christine M.; Teat, Simon J. [Lawrence Berkeley National Laboratory, Berkeley, CA (United States). Advanced Light Source; Shuh, David K. [Lawrence Berkeley National Laboratory, Berkeley, CA (United States). Chemical Sciences Div.

2016-04-04

Efficient separation processes for recovering uranium and plutonium from spent nuclear fuel are essential to the development of advanced nuclear fuel cycles. The performance characteristics of a new salt-free complexing and reducing reagent, glutarimidedioxime (H{sub 2}A), are reported for recovering plutonium in a PUREX process. With a phase ratio of organic to aqueous of up to 10:1, plutonium can be effectively stripped from 30 % tributyl phosphate (TBP) in kerosene into 1M HNO{sub 3} with H{sub 2}A. The complexation-reduction mechanism is illustrated with the combination of UV/Vis absorption spectra and the crystal structure of a Pu{sup IV} complex with the reagent. The fast stripping rate and the high efficiency for stripping Pu{sup IV}, through the complexation-reduction mechanism, is suitable for use in centrifugal contactors with very short contact/resident times, thereby offering significant advantages over conventional processes.

Ultratrace analysis of uranium and plutonium by mass spectrometry

International Nuclear Information System (INIS)

Wogman, N.A.; Wacker, J.F.; Olsen, K.B.; Petersen, S.L.; Farmer, O.T.; Kelley, J.M.; Eiden, G.C.; Maiti, T.C.

2002-01-01

Full text: Uranium and plutonium have traditionally been analyzed using alpha energy spectrometry. Both isotopic compositions and elemental abundances can be characterized on samples containing microgram to milligram quantities of uranium and nanogram to microgram quantities of plutonium. In the past ten years or so, considerable interest has developed in measuring nanograms quantities of uranium and sub-picogram quantities of plutonium in environmental samples. Such measurements require high sensitivity and as a consequence, sensitive mass spectrometric-based methods have been developed. Thus, the analysis of uranium and plutonium have gone from counting decays to counting atoms, with considerable increases in both sensitivity and precision for isotopic measurements. At the Pacific Northwest National Laboratory (PNNL), we have developed highly sensitive methods to analyze uranium and plutonium in environmental samples. The development of an ultratrace analysis capability for measuring uranium and plutonium has arisen from a need to detect and characterize environmental samples for signatures associated with nuclear industry processes. Our most sensitive well-developed methodologies employ thermal ionization mass spectrometry (TIMS), however, recent advances in inductively coupled plasma mass spectrometry (ICP-MS) have shown considerable promise for use in detecting uranium and plutonium at ultratrace levels. The work at PNNL has included the development of both chemical separation and purification techniques, as well as the development of mass spectrometric instrumentation and techniques. At the heart of our methodology for TIMS analysis is a procedure that utilizes 100-microliter-volumes of analyte for chemical processing to purify, separate, and load actinide elements into resin beads for subsequent mass spectrometric analysis. The resin bead technique has been combined with a thorough knowledge of the physicochemistry of thermal ion emission to achieve

Plutonium separation by reduction stripping. Application to processing of mixed oxide (U,Pu)O2 fuel fabrication wastes

International Nuclear Information System (INIS)

Arnal, Thierry; Cousinou, Gerard; Ganivet, Michel.

1978-11-01

A procedure is described for separating plutonium from a uranium VI and plutonium IV mixture contained in an organic phase (tributyl phosphate diluted in dodecane). This separation is obtained by extracting the plutonium III using two organic reducers: hydrazine and paraminophenol. Paraminophenol has excellent reducing qualities, similar to those of ferrous sulphamate, but has the added advantage of not contaminating extracted plutonium. This procedure is currently used in processing production wastes from mixed oxide (U,Pu)O 2 fuels; the installation using this procedure is described in detail in this paper. Operating results show the remarkable efficiency of this procedure: the separated plutonium and uranium mass flows have been increased to 185 and 350 g.h -1 respectively; the uranium contains less than 0.1 ppm of plutonium on completion of the purification cycle [fr

Introducing advanced nuclear fuel cycles in Canada

International Nuclear Information System (INIS)

Duret, M.F.

1978-05-01

The ability of several different advanced fuel cycles to provide energy for a range of energy growth scenarios has been examined for a few special situations of interest in Canada. Plutonium generated from the CANDU-PHW operating on natural uranium is used to initiate advanced fuel cycles in the year 2000. The four fuel cycles compared are: 1) natural uranium in the CANDU-PHW; 2) high burnup thorium cycle in the CANDU-PHW; 3) self-sufficient thorium cycle in the CANDU-PHW; 4) plutonium-uranium cycle in a fast breeder reactor. The general features of the results are quite clear. While any plutonium generated prior to the introduction of the advanced fuel cycle remains, system requirements for natural uranium for each of the advanced fuel cycles are the same and are governed by the rate at which plants operating on natural uranium can be retired. When the accumulated plutonium inventory has been entirely used, natural uranium is again required to provide inventory for the advanced fuel cycle reactors. The time interval during which no uranium is required varies only from about 25 to 40 years for both thorium cycles, depending primarily on the energy growth rate. The breeder does not require the entire plutonium inventory produced and so would call for less processing of fuel from the PHW reactors. (author)

METHOD OF PRODUCING PLUTONIUM TETRAFLUORIDE

Science.gov (United States)

Tolley, W.B.; Smith, R.C.

1959-12-15

A process is presented for preparing plutonium tetrafluoride from plutonium(IV) oxalate. The oxalate is dried and decomposed at about 300 deg C to the dioxide, mixed with ammonium bifluoride, and the mixture is heated to between 50 and 150 deg C whereby ammonium plutonium fluoride is formed. The ammonium plutonium fluoride is then heated to about 300 deg C for volatilization of ammonium fluoride. Both heating steps are preferably carried out in an inert atmosphere.

Plutonium roundtable discussion

International Nuclear Information System (INIS)

Penneman, R.A.

1982-01-01

The roundtable discussion began with remarks by the chairman who pointed out the complicated nature of plutonium chemistry. Judging from the papers presented at this symposium, he noticed a pattern which indicated to him the result of diminished funding for investigation of basic plutonium chemistry and funding focused on certain problem areas. Dr. G.L. silver pointed to plutonium chemists' erroneous use of a simplified summary equation involving the disproportionation of Pu(EV) and their each of appreciation of alpha coefficients. To his appreciation of alpha coefficients. To his charges, Dr. J.T. Bell spoke in defense of the chemists. This discussion was followed by W.W. Schulz's comments on the need for experimental work to determine solubility data for plutonium in its various oxidation states under geologic repository conditions. Discussion then turned to plutonium pyrachemical process with Dana C. Christensen as the main speaker. This paper presents edited versions of participants' written version

Direct oxide reduction (DOR) solvent salt recycle in pyrochemical plutonium recovery operations

International Nuclear Information System (INIS)

Fife, K.W.; Bowersox, D.F.; Davis, C.C.; McCormick, E.D.

1987-02-01

One method used at Los Alamos for producing plutonium metal is to reduce the oxide with calcium metal in molten CaCl 2 at 850 0 C. The solvent CaCl 2 from this reduction step is currently discarded as low-level radioactive waste because it is saturated with the reaction by-product, CaO. We have developed and demonstrated a molten salt technique for rechlorinating the CaO, thereby regenerating the CaCl 2 and incorporating solvent recycle into the batch PuO 2 reduction process. We discuss results from the process development experiments and present our plans for incorporating the technique into an advanced design for semicontinuous plutonium metal production

The first milligrams of plutonium

International Nuclear Information System (INIS)

Goldschmidt, B.

1996-01-01

This paper relates the discovery of the different plutonium chemical extraction processes in their historical context. The first experiments started during the second world war in 1942 with the American ''Metallurgical Laboratory'' project which brought together Arthur Compton, Enrico Fermi and Glenn Seaborg. During the same period, a competitive English-Canadian project, the ''Montreal Project'', was carried out to test different plutonium solvent extraction techniques. The author participated in both projects and joined the CEA in 1946, where he was in charge of the uranium and plutonium chemistry. By the end of 1949, his team could isolate the first milligrams of French plutonium from uranium oxide pellets of the ZOE reactor. In the beginning of 1952 he developed with his team the PUREX process. (J.S.)

Decontamination and demolition of a former plutonium processing facility's process exhaust system, firescreen, and filter plenum buildings

International Nuclear Information System (INIS)

LaFrate, P.J. Jr.; Stout, D.S.; Elliott, J.W.

1996-01-01

The Los Alamos National Laboratory (LANL) Decommissioning Project has decontaminated, demolished, and decommissioned a process exhaust system, two filter plenum buildings, and a firescreen plenum structure at Technical Area 21 (TA-2 1). The project began in August 1995 and was completed in January 1996. These high-efficiency particulate air (HEPA) filter plenums and associated ventilation ductwork provided process exhaust to fume hoods and glove boxes in TA-21 Buildings 2 through 5 when these buildings were active plutonium and uranium processing and research facilities. This paper summarizes the history of TA-21 plutonium and uranium processing and research activities and provides a detailed discussion of integrated work process controls, characterize-as-you-go methodology, unique engineering controls, decontamination techniques, demolition methodology, waste minimization, and volume reduction. Also presented in detail are the challenges facing the LANL Decommissioning Project to safely and economically decontaminate and demolish surplus facilities and the unique solutions to tough problems. This paper also shows the effectiveness of the integrated work package concept to control work through all phases

Decontamination and demolition of a former plutonium processing facility's process exhaust system, firescreen, and filter plenum buildings

International Nuclear Information System (INIS)

LaFrate, P.J. Jr.; Stout, D.S.; Elliott, J.W.

1996-01-01

The Los Alamos National Laboratory (LANL) Decommissioning Project has decontaminated, demolished, and decommissioned a process exhaust system, two filter plenum buildings, and a firescreen plenum structure at Technical Area 21 (TA-21). The project began in August 1995 and was completed in January 1996. These high-efficiency particulate air (HEPA) filter plenums and associated ventilation ductwork provided process exhaust to fume hoods and glove boxes in TA-21 Buildings 2 through 5 when these buildings were active plutonium and uranium processing and research facilities. This paper summarizes the history of TA-21 plutonium and uranium processing and research activities and provides a detailed discussion of integrated work process controls, characterize-as-you-go methodology, unique engineering controls, decontamination techniques, demolition methodology, waste minimization, and volume reduction. Also presented in detail are the challenges facing the LANL Decommissioning Project to safely and economically decontaminate and demolish surplus facilities and the unique solutions to tough problems. This paper also shows the effectiveness of the integrated work package concept to control work through all phases

Glutarimidedioxime: a complexing and reducing reagent for plutonium recovery from spent nuclear fuel reprocessing

Energy Technology Data Exchange (ETDEWEB)

Xian, Liang [Radiochemistry Department, China Institute of Atomic Energy, Beijing (China); Tian, Guoxin [Radiochemistry Department, China Institute of Atomic Energy, Beijing (China); Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA (United States); Beavers, Christine M.; Teat, Simon J. [Advanced Light Source, Lawrence Berkeley National Laboratory, Berkeley, CA (United States); Shuh, David K. [Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA (United States)

2016-04-04

Efficient separation processes for recovering uranium and plutonium from spent nuclear fuel are essential to the development of advanced nuclear fuel cycles. The performance characteristics of a new salt-free complexing and reducing reagent, glutarimidedioxime (H{sub 2}A), are reported for recovering plutonium in a PUREX process. With a phase ratio of organic to aqueous of up to 10:1, plutonium can be effectively stripped from 30 % tributyl phosphate (TBP) in kerosene into 1 m HNO{sub 3} with H{sub 2}A. The complexation-reduction mechanism is illustrated with the combination of UV/Vis absorption spectra and the crystal structure of a Pu{sup IV} complex with the reagent. The fast stripping rate and the high efficiency for stripping Pu{sup IV}, through the complexation-reduction mechanism, is suitable for use in centrifugal contactors with very short contact/resident times, thereby offering significant advantages over conventional processes. (copyright 2016 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

Optimum Condition for Plutonium Electrodeposition Process in Radiochemistry and Environment Laboratory, Nuclear Malaysia

International Nuclear Information System (INIS)

Yii, Mei-Wo; Abdullah Siddiqi Ismail

2014-01-01

Determination of alpha emitting plutonium radionuclides such as Pu-238, Pu-239 and Pu-240 concentrations inside a sample require lots of radiochemistry purification process to separate them from other interfering alpha emitters. These pure isotopes are then been electrodeposited onto a stainless steel disc and quantified using alpha spectrometry counter. In Radiochemistry and Environment Laboratory (RAS), Nuclear Malaysia, the quantification is done by comparing these isotopes with the recovery of known amount plutonium tracer, Pu-242, that been added into the sample prior analysis. This study been conducted to find the optimum conditions for the electrolysis process used at RAS. Four variable parameters that may interfere the percentage recovery of tracer hence the current, cathode to anode distance, pH and electrolysis duration had been identify and studied. Study was carry out using Pu-242 standard solution and the deposition disc was counted using Zinc Sulphite (silver) counter. Studies outcome suggested that the optimum conditions to reduce plutonium ion happens at 1-1.1 ampere of current, 3-5 mm of electrodes distance, pH 2.2-2.5 and a minimal electrolysis duration of 2 hours. (author)

The establishment of in-process plutonium mass equation in Rokkasho Reprocessing Plant

International Nuclear Information System (INIS)

Yamaya, Kosuke; Ebata, Takashi; Yamazaki, Yoshihiro; Kawai, Akio; Iwamoto, Tomonori

2008-01-01

At Rokkasho Reprocessing Plant (RRP), Active Test (AT) using actual spent fuels for the final confirmation of the equipment and the system has been performed toward the commercial operation. From the safeguards viewpoint, performance of material accountancy equipment is confirmed and data for evaluating parameters of the inspection equipment is obtained by making use of the AT period. RRP is applied to Near Real Time material Accountancy (NRTA). Under the NRTA scheme, the inventory at a cut-off time during process operation needs to be accounted for. There are some un-measurable inventories of plutonium in the process, which will be calculated from inventory estimation equations. The amount of these plutonium inventories calculated from the equations is so large that it is essential to improve the inventory estimation equations to be quite accurate. Therefore, correctness of the inventory estimation equations is evaluated by using process operation data obtained during AT. This paper describes the results of evaluating the inventory estimation equations by using the process operation data and the NRTA procedure under continuous operating condition as well. (author)

Materials measurement and accounting in an operating plutonium conversion and purification process. Phase I. Process modeling and simulation

International Nuclear Information System (INIS)

Thomas, C.C. Jr.; Ostenak, C.A.; Gutmacher, R.G.; Dayem, H.A.; Kern, E.A.

1981-04-01

A model of an operating conversion and purification process for the production of reactor-grade plutonium dioxide was developed as the first component in the design and evaluation of a nuclear materials measurement and accountability system. The model accurately simulates process operation and can be used to identify process problems and to predict the effect of process modifications

Plutonium Disposition Now exclamation point

International Nuclear Information System (INIS)

Buckner, M.R.

1995-01-01

A means for use of existing processing facilities and reactors for plutonium disposition is described which requires a minimum capital investment and allows rapid implementation. The scenario includes interim storage and processing under IAEA control, and fabrication into MOX fuel in existing or planned facilities in Europe for use in operating reactors in the two home countries. Conceptual studies indicate that existing Westinghouse four-loop designs can safety dispose of 0.94 MT of plutonium per calendar year. Thus, it would be possible to consume the expected US excess stockpile of about 50 MT in two to three units of this type, and it is highly likely that a comparable amount of the FSU excess plutonium could be deposed of in a few VVER-1000's. The only major capital project for this mode of plutonium disposition would be the weapons-grade plutonium processing which could be done in a dedicated international facility or using existing facilities in the US and FSU under IAEA control. This option offers the potential for quick implementation at a very low cost to the governments of the two countries

Plutonium Immobilization Can Loading Conceptual Design

Energy Technology Data Exchange (ETDEWEB)

Kriikku, E.

1999-05-13

'The Plutonium Immobilization Facility will encapsulate plutonium in ceramic pucks and seal the pucks inside welded cans. Remote equipment will place these cans in magazines and the magazines in a Defense Waste Processing Facility (DWPF) canister. The DWPF will fill the canister with glass for permanent storage. This report discusses the Plutonium Immobilization can loading conceptual design and includes a process block diagram, process description, preliminary equipment specifications, and several can loading issues. This report identifies loading pucks into cans and backfilling cans with helium as the top priority can loading development areas.'

Plutonium Immobilization Can Loading Conceptual Design

International Nuclear Information System (INIS)

Kriikku, E.

1999-01-01

'The Plutonium Immobilization Facility will encapsulate plutonium in ceramic pucks and seal the pucks inside welded cans. Remote equipment will place these cans in magazines and the magazines in a Defense Waste Processing Facility (DWPF) canister. The DWPF will fill the canister with glass for permanent storage. This report discusses the Plutonium Immobilization can loading conceptual design and includes a process block diagram, process description, preliminary equipment specifications, and several can loading issues. This report identifies loading pucks into cans and backfilling cans with helium as the top priority can loading development areas.'

Progress on plutonium stabilization

Energy Technology Data Exchange (ETDEWEB)

Hurt, D. [Defense Nuclear Facilities Safety Board, Washington, DC (United States)

1996-05-01

The Defense Nuclear Facilities Safety Board has safety oversight responsibility for most of the facilities where unstable forms of plutonium are being processed and packaged for interim storage. The Board has issued recommendations on plutonium stabilization and has has a considerable influence on DOE`s stabilization schedules and priorities. The Board has not made any recommendations on long-term plutonium disposition, although it may get more involved in the future if DOE develops plans to use defense nuclear facilities for disposition activities.

Progress on plutonium stabilization

International Nuclear Information System (INIS)

Hurt, D.

1996-01-01

The Defense Nuclear Facilities Safety Board has safety oversight responsibility for most of the facilities where unstable forms of plutonium are being processed and packaged for interim storage. The Board has issued recommendations on plutonium stabilization and has has a considerable influence on DOE's stabilization schedules and priorities. The Board has not made any recommendations on long-term plutonium disposition, although it may get more involved in the future if DOE develops plans to use defense nuclear facilities for disposition activities

Modeling of Diffusion of Plutonium in Other Metals and of Gaseous Species in Plutonium-Based Systems

International Nuclear Information System (INIS)

Cooper, Bernard R.; Gayanath W. Fernando; Beiden, S.; Setty, A.; Sevilla, E.H.

2004-01-01

Establish standards for temperature conditions under which plutonium, uranium, or neptunium from nuclear wastes permeates steel, with which it is in contact, by diffusion processes. The primary focus is on plutonium because of the greater difficulties created by the peculiarities of face-centered-cubic-stabilized (delta) plutonium (the form used in the technology generating the waste)

Review of major plutonium pyrochemical technology

International Nuclear Information System (INIS)

Moser, W.S.; Navratil, J.D.

1983-01-01

The past twenty years have seen significant growth in the development and application of pyrochemical technology for processing of plutonium. For particular feedstocks and specific applications, non-aqueous high-temperature processes offer key advantages over conventional hydrometallurgical systems. Major processes in use today include: (1) direct oxide reduction for conversion of PuO 2 to metal, (2) molten salt extraction for americium removal from plutonium, (3) molten salt electrorefining for Pu purification, and (4) hydriding to remove plutonium from host substrates. This paper reviews current major pyrochemical processes from the classical calcination-hydrofluorination-bomb reduction sequence through new techniques under development. Each process is presented and brief descriptions of production equipment are given. 47 references, 5 figures

Plutonium decontamination studies using Reverse Osmosis

International Nuclear Information System (INIS)

Plock, C.E.; Travis, T.N.

1980-01-01

Water in batches of 45 gallons each, from a creek crossing the Rocky Flats Plant, was transferred to the Reverse Osmosis (RO) laboratory for experimental testing. The testing involved using RO for plutonium decontamination. For each test, the water was spiked with plutonium, had its pH adjusted, and was then processed by RO. At a water recovery level of 87%, the plutonium decontamination factors ranged from near 100 to 1200, depending on the pH of the processed water

Uranium-plutonium fuel for fast reactors

International Nuclear Information System (INIS)

Antipov, S.A.; Astafiev, V.A.; Clouchenkov, A.E.; Gustchin, K.I.; Menshikova, T.S.

1996-01-01

Technology was established for fabrication of MOX fuel pellets from co-precipitated and mechanically blended mixed oxides. Both processes ensure the homogeneous structure of pellets readily dissolvable in nitric acid upon reprocessing. In order to increase the plutonium charge in a reactor-burner a process was tested for producing MOX fuel with higher content of plutonium and an inert diluent. It was shown that it is feasible to produce fuel having homogeneous structure and the content of plutonium up to 45% mass

Plutonium recovery from carbonate wash solutions

International Nuclear Information System (INIS)

Gray, J.H.; Reif, D.J.; Chostner, D.F.; Holcomb, H.P.

1991-01-01

540Periodically higher than expected levels of plutonium are found in carbonate solutions used to wash second plutonium cycle solvent. The recent accumulation of plutonium in carbonate wash solutions has led to studies to determine the cause of that plutonium accumulation, to evaluate the quality of all canyon solvents, and to develop additional criteria needed to establish when solvent quality is acceptable. Solvent from three canyon solvent extraction cycles was used to evaluate technology required to measure tributyl phosphate (TBP) degradation products and was used to evaluate solvent quality criteria during the development of plutonium recovery processes. 1 fig

Plutonium spectrophotometric analysis

International Nuclear Information System (INIS)

Esteban, A.; Cassaniti, P.; Orosco, E.H.

1990-01-01

Plutonium ions in solution have absorption spectra so different that it is possible to use them for analytical purposes. Detailed studies have been performed in nitric solutions. Some very convenient methods for the determination of plutonium and its oxidation states, especially the ratios Pu(III):Pu(IV) and Pu(IV):Pu(VI) in a mixture of both, have been developed. These methods are described in this paper, including: a) Absorption spectra for plutonium (III), (IV), (VI) and mixtures. b) Relative extinction coefficients for the above mentioned species. c) Dependences of the relative extinction coefficients on the nitric acid concentration and the plutonium VI deviation from the Beer-Lambert law. The developed methods are simple and rapid and then, suitable in process control. Accuracy is improved when relative absorbance measurements are performed or controlled the variables which have effect on the spectra and extinction coefficients. (Author) [es

Plutonium estimation in the process solutions and oxide dissolved audit samplers by potentiometry using memo titrator

International Nuclear Information System (INIS)

Kumaraguru, K.; Shukla, Y.D.; Vijayan, K.; Ramamoorthy, N.; Jambunathan, U.; Kapoor, S.C.

1990-01-01

Potentiometric method is employed by using memotitrator coupled with combined electrode for the estimation of plutonium. The estimations are carried out on the process samples and the acid dissolved samples for auditing, in the concentration range of 5 g/l to 20 g/l. The chemical procedure is: i)oxidising plutonium to higher oxidation state by silver oxide, ii)reducing the same by adding excess ferrous, and iii)titrating potassium dichromate against the unreacted ferrous. The plutonium content is computed from ferrous consumed in the reaction. The average percentage error of the method is +/-0.27. The values obtained are in close agreement with those obtained by coulometry. (author)

Investigation of plutonium (4) hydroxoformates

International Nuclear Information System (INIS)

Andryushin, V.G.; Belov, V.A.; Galaktionov, S.V.; Kozhevnikov, P.B.; Matyukha, V.A.; Shmidt, V.S.

1982-01-01

Deposition processes of plutonium (4) hydroxoformates in the system Pu(NO 3 ) 4 -HNO 3 -HCoOH-N6 4 OH-H 2 O have been studied in pH range 0.2-10.7 at total plutonium concentration in the system 100 g/l. It is shown that under the conditions plutonium (4) hydrolysis takes place with the formation of hydroxoformates. A local maximum of plutonium (4) hydroxoformate solubility in the range pH=3.8-4.8, which is evidently conditioned by the formation of soluble formate complex of plutonium in the region, is pointed out. The basic plutonium (4) formates of the composition PuOsub(x)(OH)sub(y)(COOH)sub(4-2x-y)xnHsub(2)O, where 1,3 >=x >= 0.7, 1.7 >= y >= 1.0 and n=1.5-7.0, are singled out, their thermal stability being studied. Density of the crystals and plutonium dioxide, formed during their thermal decomposition, is measured. It is established that for plutonium (4) hydroxoformates common regularities of the influence of salt composition (OH - -, CHOO - - and H 2 O-group numbers in the mulecule) on position of temperature decomposition effects and on the density of compounds, which have been previously found during the study of thorium and plutonium hydroxosalts are observed. It is shown that the density of plutonium dioxide decreases with the increase of hydration and hydrolysis degree of the initial plutonium hydroxoformate

DOE plutonium disposition study: Pu consumption in ALWRs

International Nuclear Information System (INIS)

1993-01-01

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

Modelling of uranium/plutonium splitting in purex process

International Nuclear Information System (INIS)

Boullis, B.; Baron, P.

1987-06-01

A mathematical model simulating the highly complex uranium/plutonium splitting operation in PUREX process has been achieved by the french ''Commissariat a l'Energie Atomique''. The development of such a model, which includes transfer and redox reactions kinetics for all the species involved, required an important experimental work in the field of basis chemical data acquisition. The model has been successfully validated by comparison of its results with those of specific trials achieved (at laboratory scale), and with the available results of the french reprocessing units operation. It has then been used for the design of french new plants splitting operations

Waste minimization and the goal of an environmentally benign plutonium processing facility: A strategic plan

International Nuclear Information System (INIS)

Pillay, K.K.S.

1994-02-01

To maintain capabilities in nuclear weapons technologies, the Department of Energy (DOE) has to maintain a plutonium processing facility that meets all the current and emerging standards of environmental regulations. A strategic goal to transform the Plutonium Processing Facility at Los Alamos into an environmentally benign operation is identified. A variety of technologies and systems necessary to meet this goal are identified. Two initiatives now in early stages of implementation are described in some detail. A highly motivated and trained work force and a systems approach to waste minimization and pollution prevention are necessary to maintain technical capabilities, to comply with regulations, and to meet the strategic goal

Plutonium in nature; Le plutonium dans la nature

Energy Technology Data Exchange (ETDEWEB)

Madic, C.

1994-12-31

Plutonium in nature comes from natural sources and anthropogenic ones. Plutonium at the earth surface comes principally from anthropogenic sources. It is easily detectable in environment. The plutonium behaviour in environment is complex. It seems necessary for the future to reduce releases in environment, to improve predictive models of plutonium behaviour in geosphere, to precise biological impact of anthropogenic plutonium releases.

Advanced PWR Core Design with Siemens High-Plutonium-Content MOX Fuel Assemblies

International Nuclear Information System (INIS)

Dieter Porsch; Gerhard Schlosser; Hans-Dieter Berger

2000-01-01

The Siemens experience with plutonium recycling dates back to the late 1960s. Over the years, extensive research and development programs were performed for the qualification of mixed-oxide (MOX) technology and design methods. Today's typical reload enrichments for uranium and MOX fuel assemblies and modern core designs have become more demanding with respect to accuracy and reliability of design codes. This paper presents the status of plutonium recycling in operating high-burnup pressurized water reactor (PWR) cores. Based on actual examples, it describes the validation status of the design methods and stresses current and future needs for fuel assembly and core design including those related to the disposition of weapons-grade plutonium

Strategies for the plutonium utilization

International Nuclear Information System (INIS)

Zouain, D.M.; Lima, J.O.V.; Sakamoto, L.H.

1981-11-01

A review of the activities involving plutonium (its recycle, utilization and technological status and perspectives) is done. These informations are useful for an economic viability study for the plutonium utilization in thermal reactors (recycling) and in fast breeders reactor (FBR), trying to collect the major number of informations about these subjects. The initial phase describes the present status and projections of plutonium accumulation and requirements. Then, the technological process are described and some strategies are analyzed. (E.G.) [pt

Plutonium accident resistant container project

International Nuclear Information System (INIS)

Andersen, J.A.

1978-05-01

The PARC (plutonium accident resistant container) project resulted in the design, development, and certification testing of a crashworthy air-transportable plutonium package (shipping container) for certification by the USNRC. This PAT-1 (plutonium air transportable) package survives a very severe sequential test program of impact, crush, puncture, slash, burn, and water immersion. There is also an individual hydrostatic pressure test. The package has a payload mass capacity of 2 kg of PuO2 and a thermal capacity of 25 watts. The design rationale for very high energy absorption (impact, crush, puncture, and slash protection) with residual high-level fire protection, resulted in a reasonalby small air-transportable package, advancing the packaging state-of-art. Optimization design iterations were utilized in the areas of impact energy absorption and stress and thermal analysis. Package test results are presented in relation to radioactive materials containment acceptance criteria, shielding and criticality standards

An introduction to the Advanced Testing Line for Actinide Separations (ATLAS)

International Nuclear Information System (INIS)

Pope, N.G.; Yarbro, S.L.; Schreiber, S.B.; Day, R.S.

1992-03-01

The Advanced Testing Line for Actinide Separations (ATLAS) will evaluate promising plutonium recovery process modifications and new technologies. It combines advances in process chemistry, process control, process analytical chemistry, and process engineering. ATLAS has a processing capability equal to other recovery systems but without the pressure to achieve predetermined recovery quotas

Experience with thermal recycle of plutonium and uranium

International Nuclear Information System (INIS)

Beer, O.; Schlosser, G.; Spielvogel, F.

1985-01-01

The Federal Republic of Germany (FRG) decided to close the fuel cycle by erecting the reprocessing plant WA350 at Wackersdorf. As long as the plutonium supply from reprocessing plants exceeds the plutonium demand of fast breeder reactors, recycling of plutonium in LWR's is a convenient solution by which a significant advanced uranium utilization is achieved. The demonstration of plutonium recycling performed to date in the FRG in BWR's and PWR's shows that thermal plutonium recycling on an industrial scale is feasible and that the usual levels of reliability and safety can be achieved in reactor operation. The recycling of reprocessed uranium is presently demonstrated in the FRG, too. As regards fuel cycle economy thermal recycling allows savings in natural uranium and separative work. Already under present cost conditions the fuel cycle costs for mixed oxide or enriched reprocessed uranium fuel assemblies are equal or even lower than for usual uranium fuel assemblies

DOE Plutonium Disposition Study: Pu consumption in ALWRs

International Nuclear Information System (INIS)

1993-01-01

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

Pyrochemical recovery of plutonium fluoride reduction slag

International Nuclear Information System (INIS)

Christensen, D.C.; Rayburn, J.A.

1983-07-01

A process was developed for the pyrochemical recovery of plutonium from residues resulting from the PuF 4 reduction process. The process involves crushing the CaF 2 slag and dissolving it at 800 0 C in a CaCl 2 solvent. The plutonium, which exists either as finely divided metal or as incompletely reduced fluoride salt, is reduced to metal and/or allowed to coalesce as a massive button in the bottom of the reaction crucible. The recovery of plutonium in a 1-day cycle averaged 96%; all of the resulting residues were discardable

Advanced plutonium assembly (apa): evolution of the concept, neutron and thermal-mechanic constraints

International Nuclear Information System (INIS)

Porta, J.; Gastaldi, B.; Krakowiak-Aillaud, C.; Buffe, L.

2002-01-01

The APA concept was developed with the aim of increasing the PWR capacity to burn plutonium emerging from the recycling of irradiated fuels in the French park of nuclear power plants. At first, a concept using annular pins was optimised to allow a good consumption of plutonium while preserving an acceptable neutron control. To cope with the technological problems and those posed by the manufacture of these annular pins, an alternative concept is presented here. It poses as initial conditions the conservation of both the plutonium balance and the respect of the reactivity control. (authors)

Nuclear fuel: modelling the advanced plutonium assembly

International Nuclear Information System (INIS)

Kaoua, Th.; Lenain, R.

2004-01-01

The benefits of modeling in the nuclear sector are illustrated by the example of the design study for a new plutonium fuel assembly, APA, capable of ensuring maximum consumption of this fuel in pressurized-water reactors. Beyond the physical design of the assembly and its integration into the reactor, this serves for the working out of a complete materials flow and assists in modeling production from the entire inventory of nuclear power stations. (authors)

Nuclear fuel: modelling the advanced plutonium assembly

International Nuclear Information System (INIS)

N'kaoua, Th.; Lenain, R.

2002-01-01

The benefits of modeling in the nuclear sector are illustrated by the example of the design study for a new plutonium fuel assembly, APA, capable of ensuring maximum consumption of this fuel in pressurized-water reactors. Beyond the physical design of the assembly and its integration into the reactor, this serves for the working out of a complete materials flow and assists in modeling production from the entire inventory of nuclear power stations. (authors)

Method to manufacture a nuclear fuel from uranium-plutonium monocarbide or uranium-plutonium mononitride

International Nuclear Information System (INIS)

Krauth, A.; Mueller, N.

1977-01-01

Pure uranium carbide or nitride is converted with plutonium oxide and carbon (all in powder form) to uranium-plutonium monocarbide or mononitride by cold pressing and sintering at about 1600 0 C. Pure uranium carbide or uranium nitride powder is firstly prepared without extensive safety measures. The pure uranium carbide or nitride powder can also be inactivated by using chemical substances (e.g. stearic acid) and be handled in air. The sinterable uranium carbide or nitride powder (or also granulate) is then introduced into the plutonium line and mixed with a nonstoichiometrically adjusted, prereacted mixture of plutonium oxide and carbon, pressed to pellets and reaction sintered. The surface of the uranium-plutonium carbide (higher metal content) can be nitrated towards the end of the sinter process in a stream of nitrogen. The protective layer stabilizes the carbide against the water and oxygen content in air. (IHOE) [de

The chemistry of tributyl phosphate at elevated temperatures in the Plutonium Finishing Plant Process Vessels

International Nuclear Information System (INIS)

Barney, G.S.; Cooper, T.D.

1994-01-01

Potentially violent chemical reactions of the tributyl phosphate solvent used by the Plutonium Finishing Plant at the Hanford Site were investigated. There is a small probability that a significant quantity of this solvent could be accidental transferred to heated process vessels and react there with nitric acid or plutonium nitrate also present in the solvent extraction process. The results of laboratory studies of the reactions show that exothermic oxidation of tributyl phosphate by either nitric acid or actinide nitrates is slow at temperatures expected in the heated vessels. Less than four percent of the tributyl phosphate will be oxidized in these vented vessels at temperatures between 125 degrees C and 250 degrees C because the oxidant will be lost from the vessels by vaporization or decomposition before the tributyl phosphate can be extensively oxidized. The net amounts of heat generated by oxidation with concentrated nitric acid and with thorium nitrate (a stand-in for plutonium nitrate) were determined to be about -150 and -220 joules per gram of tributyl phosphate initially present, respectively. This is not enough heat to cause violent reactions in the vessels. Pyrolysis of the tributyl phosphate occurred in these mixtures at temperatures of 110 degrees C to 270 degrees C and produced mainly 1-butene gas, water, and pyrophosphoric acid. Butene gas generation is slow at expected process vessel temperatures, but the rate is faster at higher temperatures. At 252 degrees C the rate of butene gas generated was 0.33 g butene/min/g of tributyl phosphate present. The measured heat absorbed by the pyrolysis reaction was 228 J/g of tributyl phosphate initially present (or 14.5 kcal/mole of tributyl phosphate). Release of flammable butene gas into process areas where it could ignite appears to be the most serious safety consideration for the Plutonium Finishing Plant

The chemistry of tributyl phosphate at elevated temperatures in the Plutonium Finishing Plant Process Vessels

Energy Technology Data Exchange (ETDEWEB)

Barney, G.S.; Cooper, T.D.

1994-06-01

Potentially violent chemical reactions of the tributyl phosphate solvent used by the Plutonium Finishing Plant at the Hanford Site were investigated. There is a small probability that a significant quantity of this solvent could be accidental transferred to heated process vessels and react there with nitric acid or plutonium nitrate also present in the solvent extraction process. The results of laboratory studies of the reactions show that exothermic oxidation of tributyl phosphate by either nitric acid or actinide nitrates is slow at temperatures expected in the heated vessels. Less than four percent of the tributyl phosphate will be oxidized in these vented vessels at temperatures between 125{degrees}C and 250{degrees}C because the oxidant will be lost from the vessels by vaporization or decomposition before the tributyl phosphate can be extensively oxidized. The net amounts of heat generated by oxidation with concentrated nitric acid and with thorium nitrate (a stand-in for plutonium nitrate) were determined to be about -150 and -220 joules per gram of tributyl phosphate initially present, respectively. This is not enough heat to cause violent reactions in the vessels. Pyrolysis of the tributyl phosphate occurred in these mixtures at temperatures of 110{degrees}C to 270{degrees}C and produced mainly 1-butene gas, water, and pyrophosphoric acid. Butene gas generation is slow at expected process vessel temperatures, but the rate is faster at higher temperatures. At 252{degrees}C the rate of butene gas generated was 0.33 g butene/min/g of tributyl phosphate present. The measured heat absorbed by the pyrolysis reaction was 228 J/g of tributyl phosphate initially present (or 14.5 kcal/mole of tributyl phosphate). Release of flammable butene gas into process areas where it could ignite appears to be the most serious safety consideration for the Plutonium Finishing Plant.

Cation exchange process for recovery of plutonium from laboratory solutions containing chloride

International Nuclear Information System (INIS)

Gray, L.W.

1978-10-01

A cation exchange technique was developed for the separation of plutonium from laboratory solutions containing either Pu(III) or Pu(III)--Pu(IV) mixtures in acidic solutions containing chloride ions. The procedure consists of adjusting the acid concentration to less than one molar and adjusting the valence of the plutonium ion to the (III) state, if necessary. The adjusted solution is fed to a cation exchange column and washed with distilled water to remove residual chlorides from the column. Plutonium is then eluted from the column with 5M nitric acid containing 0.34M sulfamic acid. This procedure was used to separate plutonium from 1.2M chloride solution on a production-scale column. Typical plutonium recovery was 99.97%, while greater than 96% of the original chloride was rejected

Solvent anode for plutonium purification

International Nuclear Information System (INIS)

Bowersox, D.F.; Fife, K.W.; Christensen, D.C.

1986-01-01

The purpose of this study is to develop a technique to allow complete oxidation of plutonium from the anode during plutonium electrorefining. This will eliminate the generation of a ''spent'' anode heel which requires further treatment for recovery. Our approach is to employ a solvent metal in the anode to provide a liquid anode pool throughout electrorefining. We use molten salts and metals in ceramic crucibles at 700 0 C. Our goal is to produce plutonium metal at 99.9% purity with oxidation and transfer of more than 98% of the impure plutonium feed metal from the anode into the salt and product phases. We have met these criteria in experiments on the 100 to 1000 g scale. We plan to scale our operations to 4 kg of feed plutonium and to optimize the process parameters

Plutonium helps probe protein, superconductor

International Nuclear Information System (INIS)

Anon.

1990-01-01

Scientists are finding that plutonium can be a useful research tool that may help them answer important questions in fields as diverse as biochemistry and solid-state physics. This paper reports that U.S. research involving plutonium is confined to the Department of Energy's national laboratories and centers around nuclear weapons technology, waste cleanup and disposal, and health effects. But at Los Alamos National Laboratory, scientists also are using plutonium to probe the biochemical behavior of calmodulin, a key calcium-binding protein that mediates calcium-regulated processes in biological systems. At Argonne National Laboratory, another team is trying to learn how a superconductor's properties are affected by the 5f electrons of an actinide like plutonium

Ammonium uranyl carbonate (AUC) based process of simultaneous partitioning and reconversion for uranium and plutonium in fast breeder reactors (FBRs) fuel reprocessing

International Nuclear Information System (INIS)

Govindan, P.; Palamalai, A.; Vijayan, K.S.; Subba Rao, R.V.; Venkataraman, M.; Natarajan, R.

2013-01-01

Ammonium uranyl carbonate (AUC) based process of simultaneous partitioning and reconversion for uranium and plutonium is developed for the recovery of uranium and plutonium present in spent fuel of fast breeder reactors (FBRs). Effect of pH on the solubility of carbonates of uranium and plutonium in ammonium carbonate medium is studied. Effect of mole ratios of uranium and plutonium as a function of uranium and plutonium concentration at pH 8.0-8.5 for effective separation of uranium and plutonium to each other is studied. Feasibility of reconversion of plutonium in carbonate medium is also studied. The studies indicate that uranium is selectively precipitated as AUC at pH 8.0-8.5 by adding ammonium carbonate solution leaving plutonium in the filtrate. Plutonium in the filtrate after acidified with concentrated nitric acid could also be precipitated as carbonate at pH 6.5-7.0 by adding ammonium carbonate solution. A flow sheet is proposed and evaluated for partitioning and reconversion of uranium and plutonium simultaneously in the FBR fuel reprocessing. (author)

Disposition of plutonium as non-fertile fuel for water reactors

International Nuclear Information System (INIS)

Chidester, K.; Eaton, S.L.; Ramsey, K.B.

1998-01-01

This is the final report of a three-year, Laboratory Directed Research and Development (LDRD) project at the Los Alamos National Laboratory (LANL). The original intent of this project was to investigate the possible use of a new fuel form as a means of dispositioning the declared surplus inventory of weapons-grade plutonium. The focus soon changed, however, to managing the larger and rapidly growing inventories of plutonium arising in commercial spent nuclear fuel through implementation of a new fuel form in existing nuclear reactors. LANL embarked on a parallel path effort to study fuel performance using advanced physics codes, while also demonstrating the ability to fabricate a new fuel form using standard processes in LANL's Plutonium Facility. An evolutionary fuel form was also examined which could provide enhanced performance over standard fuel forms, but which could be implemented in a much shorter time frame than a completely new fuel form. Recent efforts have focused on implementation of results into global energy models and development of follow-on funding to continue this research

Protected Plutonium Production by Transmutation of Minor Actinides for Peace and Sustainable Prosperity [O1] - Fundamentals of P{sup 3} Mechanism and Methodology Development for Plutonium Categorization

Energy Technology Data Exchange (ETDEWEB)

Saito, Masaki [Research Laboratory for Nuclear Reactor, Tokyo Institute of Technology, 2-12-1 Ookayama, Meguro, Tokyo, 1528550 (Japan)

2009-06-15

'Protected Plutonium Production (P{sup 3})' has been proposed to enhance the proliferation resistance of plutonium by the transmutation of Minor Actinides (MAs). Doping the small amount of MAs such as {sup 237}Np or {sup 241}Am with large neutron capture cross-section into the uranium fuel to enhance the production of {sup 238}Pu or {sup 242}Pu, which have high spontaneous fission neutron source or also high decay heat to makes the process of the nuclear weapon manufacture and maintenance technologically difficult, can be effective for improving the isotopic barrier of proliferation resistance of the plutonium in thermal reactors. Super weapon grade plutonium could be produced in the blanket of a conventional FBR. However, by increasing the {sup 238}Pu or {sup 242}Pu ratio in the total plutonium by MAs doping into the fresh blanket, the protected plutonium with high proliferation-resistance can be bred. A new evaluation function, 'attractiveness', defined as a ratio of potential of fission yield to the technological difficulties of nuclear explosive device, has been proposed to evaluate the proliferation resistance of Pu based on the nuclear material property for Plutonium Categorization. In the conference, the fundamentals of P{sup 3} mechanism by transmutation of MA, and the comparison of the 'attractiveness' of the Pu produced in advanced reactors based on P{sup 3} mechanism and in the conventional reactors will be presented. Instead of the geological disposal or just their burning of MAs by the fission reaction, they should be treated as valuable fertile materials to enhance the proliferation resistance of plutonium produced in the thermal and fast breeder reactors for peace and sustainable prosperity in future. Acknowledgement: Some parts of this work have been supported by the Ministry of Education, Culture, Sports, Science and Technology in Japan. (authors)

Plutonium waste incineration using pyrohydrolysis

International Nuclear Information System (INIS)

Meyer, M.L.

1991-01-01

Waste generated by Savannah River Site (SRS) plutonium operations includes a contaminated organic waste stream. A conventional method for disposing of the organic waste stream and recovering the nuclear material is by incineration. When the organic material is burned, the plutonium remains in the incinerator ash. Plutonium recovery from incinerator ash is highly dependent on the maximum temperature to which the oxide is exposed. Recovery via acid leaching is reduced for a high fired ash (>800 degree C), while plutonium oxides fired at lower decomposition temperatures (400--800 degrees C) are more soluble at any given acid concentration. To determine the feasibility of using a lower temperature process, tests were conducted using an electrically heated, controlled-air incinerator. Nine nonradioactive, solid, waste materials were batch-fed and processed in a top-heated cylindrical furnace. Waste material processing was completed using a 19-liter batch over a nominal 8-hour cycle. A processing cycle consisted of 1 hour for heating, 4 hours for reacting, and 3 hours for chamber cooling. The water gas shift reaction was used to hydrolyze waste materials in an atmosphere of 336% steam and 4.4% oxygen. Throughput ranged from 0.14 to 0.27 kg/hr depending on the variability in the waste material composition and density

Plutonium accident resistant container project

International Nuclear Information System (INIS)

Andersen, J.A.

1978-09-01

The PARC (plutonium accident resistant container) project resulted in the design, development, and certification testing of a crashworthy air-transportable plutonium package (shipping container) for certification by the USNRC (Nuclear Regulatory Commission). This PAT-1 (plutonium air transportable) package survives a very severe sequential test program of impact, crush, puncture, slash, burn, and water immersion. There is also an individual hydrostatic pressure test. The package has a payload mass capacity of 2 kg of PuO 2 and a thermal capacity of 25 watts. The design rationale for very high energy absorption (impact, crush, puncture, and slash protection) with residual high-level fire protection, resulted in a reasonably small air-transportable package, advancing the packaging state-of-art. Optimization design iterations were utilized in the areas of impact energy absorption and stress and thermal analysis. Package test results are presented in relation to radioactive materials containment acceptance criteria, shielding and criticality standards

Plutonium

International Nuclear Information System (INIS)

Watson, G.M.

1976-01-01

Discovery of the neutron made it easy to create elements which do not exist in nature. One of these is plutonium, and its isotope with mass number 239 has nuclear properties which make it both a good fuel for nuclear power reactors and a good explosive for nuclear weapons. Since it was discovered during a war the latter characteristic was put to use, but it is now evident that use of plutonium in a particular kind of nuclear reactor, the fast breeder reactor, will allow the world's resources of uranium to last for millennia as a major source of energy. Plutonium is very radiotoxic, resembling radium in this respect. Therefore the widespread introduction of fast breeder reactors to meet energy demands can be contemplated only after assurances on two points; that adequate control of the radiological hazard resulting from the handling of very large amounts of plutonium can be guaranteed, and that diversion of plutonium to illicit use can be prevented. The problems exist to a lesser degree already, since all types of nuclear reactor produce some plutonium. Some plutonium has already been dispersed in the environment, the bulk of it from atmospheric tests of nuclear weapons. (author)

Plutonium Finishing Plant safety evaluation report

International Nuclear Information System (INIS)

1995-01-01

The Plutonium Finishing Plant (PFP) previously known as the Plutonium Process and Storage Facility, or Z-Plant, was built and put into operation in 1949. Since 1949 PFP has been used for various processing missions, including plutonium purification, oxide production, metal production, parts fabrication, plutonium recovery, and the recovery of americium (Am-241). The PFP has also been used for receipt and large scale storage of plutonium scrap and product materials. The PFP Final Safety Analysis Report (FSAR) was prepared by WHC to document the hazards associated with the facility, present safety analyses of potential accident scenarios, and demonstrate the adequacy of safety class structures, systems, and components (SSCs) and operational safety requirements (OSRs) necessary to eliminate, control, or mitigate the identified hazards. Documented in this Safety Evaluation Report (SER) is DOE's independent review and evaluation of the PFP FSAR and the basis for approval of the PFP FSAR. The evaluation is presented in a format that parallels the format of the PFP FSAR. As an aid to the reactor, a list of acronyms has been included at the beginning of this report. The DOE review concluded that the risks associated with conducting plutonium handling, processing, and storage operations within PFP facilities, as described in the PFP FSAR, are acceptable, since the accident safety analyses associated with these activities meet the WHC risk acceptance guidelines and DOE safety goals in SEN-35-91

Automation of plutonium spectrophotometry

International Nuclear Information System (INIS)

Perez, J.J.; Boisde, G.; Goujon de Beauvivier, M.; Chevalier, G.; Isaac, M.

1980-01-01

Instrumentation was designed and constructed for automatic control of plutonium by molecular absorption spectrophotometry, on behalf of the reprocessing facilities, to meet two objectives: on-line measurement, of the valency state of plutonium, on by-pass, with the measured concentration covering the process concentration range up to a few mg.l -1 ; laboratory measurement of plutonium adjusted to valency VI, with operation carried out using a preparative system meeting the required containment specifications. For this two objectives, the photometer, optical cell connections are made by optical fibers resistant to β, γ radiation. Except this characteristic the devices are different according to the quality required for result [fr

Decision model for evaluating reactor disposition of excess plutonium

International Nuclear Information System (INIS)

Edmunds, T.

1995-02-01

The US Department of Energy is currently considering a range of technologies for disposition of excess weapon plutonium. Use of plutonium fuel in fission reactors to generate spent fuel is one class of technology options. This report describes the inputs and results of decision analyses conducted to evaluate four evolutionary/advanced and three existing fission reactor designs for plutonium disposition. The evaluation incorporates multiple objectives or decision criteria, and accounts for uncertainty. The purpose of the study is to identify important and discriminating decision criteria, and to identify combinations of value judgments and assumptions that tend to favor one reactor design over another

Variations of uranium and plutonium coprocessing as proliferation-resistant alternatives to the classical purex process

International Nuclear Information System (INIS)

Buckham, J.A.; Sumner, W.B.

1979-08-01

Evaluation of these alternatives for processing LWR fuel has led to the following conclusions: (1) None of the alternaives provide a pure, technical solution which completely eliminates the potential for proliferation of nuclear weapons by utilizing plutonium from the light water reactors. (2) The heat spike alternative appears feasible and provides the most effective method of rendering the LWR plutonim unattractive for weapons use. (3) The low-DF process alternate would require demonstration to: (a) determine the reliability of the in-cell recycle streams which are used to prevent reversion of the process for purification of plutonium, and (b) verify the fission product decontamination factors. (4) The alternates evaluated have no significant impacts on the design of waste treatment facilities, although the required capacities of high-level solid waste processing and high-level liquid waste storage can be significantly altered. (5) The impact of these alternate processes on fuel fabrication and other aspects of the fuel cycle requires additional evaluation

Chemical Disposition of Plutonium in Hanford Site Tank Wastes

Energy Technology Data Exchange (ETDEWEB)

Delegard, Calvin H. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Jones, Susan A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2015-05-07

This report examines the chemical disposition of plutonium (Pu) in Hanford Site tank wastes, by itself and in its observed and potential interactions with the neutron absorbers aluminum (Al), cadmium (Cd), chromium (Cr), iron (Fe), manganese (Mn), nickel (Ni), and sodium (Na). Consideration also is given to the interactions of plutonium with uranium (U). No consideration of the disposition of uranium itself as an element with fissile isotopes is considered except tangentially with respect to its interaction as an absorber for plutonium. The report begins with a brief review of Hanford Site plutonium processes, examining the various means used to recover plutonium from irradiated fuel and from scrap, and also examines the intermediate processing of plutonium to prepare useful chemical forms. The paper provides an overview of Hanford tank defined-waste–type compositions and some calculations of the ratios of plutonium to absorber elements in these waste types and in individual waste analyses. These assessments are based on Hanford tank waste inventory data derived from separately published, expert assessments of tank disposal records, process flowsheets, and chemical/radiochemical analyses. This work also investigates the distribution and expected speciation of plutonium in tank waste solution and solid phases. For the solid phases, both pure plutonium compounds and plutonium interactions with absorber elements are considered. These assessments of plutonium chemistry are based largely on analyses of idealized or simulated tank waste or strongly alkaline systems. The very limited information available on plutonium behavior, disposition, and speciation in genuine tank waste also is discussed. The assessments show that plutonium coprecipitates strongly with chromium, iron, manganese and uranium absorbers. Plutonium’s chemical interactions with aluminum, nickel, and sodium are minimal to non-existent. Credit for neutronic interaction of plutonium with these absorbers

Two-stage precipitation of plutonium trifluoride

International Nuclear Information System (INIS)

Luerkens, D.W.

1984-04-01

Plutonium trifluoride was precipitated using a two-stage precipitation system. A series of precipitation experiments identified the significant process variables affecting precipitate characteristics. A mathematical precipitation model was developed which was based on the formation of plutonium fluoride complexes. The precipitation model relates all process variables, in a single equation, to a single parameter that can be used to control particle characteristics

Chloride removal from plutonium alloy

International Nuclear Information System (INIS)

Holcomb, H.P.

1983-01-01

SRP is evaluating a program to recover plutonium from a metallic alloy that will contain chloride salt impurities. Removal of chloride to sufficiently low levels to prevent damaging corrosion to canyon equipment is feasible as a head-end step following dissolution. Silver nitrate and mercurous nitrate were each successfully used in laboratory tests to remove chloride from simulated alloy dissolver solution containing plutonium. Levels less than 10 ppM chloride were achieved in the supernates over the precipitated and centrifuged insoluble salts. Also, less than 0.05% loss of plutonium in the +3, +4, or +6 oxidation states was incurred via precipitate carrying. These results provide impetus for further study and development of a plant-scale process to recover plutonium from metal alloy at SRP

Stop plutonium

International Nuclear Information System (INIS)

2003-02-01

This press document aims to inform the public on the hazards bound to the plutonium exploitation in France and especially the plutonium transport. The first part is a technical presentation of the plutonium and the MOX (Mixed Oxide Fuel). The second part presents the installation of the plutonium industry in France. The third part is devoted to the plutonium convoys safety. The highlight is done on the problem of the leak of ''secret'' of such transports. (A.L.B.)

Plutonium dissolution from Rocky Flats Plant incinerator ash

International Nuclear Information System (INIS)

Delegard, C.H.

1985-06-01

Rockwell Hanford Operations (Rockwell) soon will commence recovery of plutonium from Rocky Flats Plant incinerator ash. In preparation for this processing, Rockwell undertook literature and laboratory studies to identify, select and optimize plutonium dissolution methods for treating the ash. Ash reburning, followed by dissolution in nitric acid containing calcium fluoride, was selected as the processing method for the ash. Recommended values of process parameters were identified. Using the selected process, 99.5% plutonium recovery was achieved, leaving about 12.7 wt % heel residue for an equal weight composite of the three ashes tested. 15 refs., 26 figs

Search for plutonium salt deposits in the plutonium extraction batteries of the Marcoule plant (1963)

International Nuclear Information System (INIS)

Bouzigues, H.; Reneaud, J.M.

1963-01-01

This report describes a method and a special apparatus making it possible to detach the insoluble plutonium salt deposits in the extraction chain of an irradiated fuel treatment plant. The process chosen allows the detection, in the extraction batteries or in the highly active chemical engineering equipment, of plutonium quantities of a few grains. After four years operation it has been impossible to detect measurable quantities of plutonium in any part of the extraction chain. The results have been confirmed by visual examinations carried out with a specially constructed endoscope. (authors) [fr

An experimental study of factors in the recovery of plutonium from combustible wastes treated by incineration, pyrolysis and other processes

International Nuclear Information System (INIS)

Bamber, D.C.; McDonald, L.A.; Roberts, W.G.; Sutcliffe, P.W.; Wilkins, J.D.

1984-01-01

The work described in this report is concerned with the incineration and pyrolysis of plutonium-contaminated combustible wastes, the leaching of the ashes and chars and the subsequent treatment of the leach solutions. A range of ashes and chars have been prepared from a range of plutonium-contaminated materials covering a variety of combustible materials (e.g. PVC, neoprene, Hypalon) and plutonium contaminants [e.g. PuO 2 , Pu(NO 3 ) 4 , (U, Pu)O 2 ]. Treatment temperatures in the range of 550-900 0 C have been investigated, the best results being obtained at or below 700 0 C with pyrolysis followed by char oxidation being the favoured process. A number of methods for treatment of the leach solutions have been considered and some have been investigated experimentally. Extraction of plutonium and americium with tributylphosphate (TBP) from a leach solution conditioned to 0.1 M H/+5 M NO 3 - has been studied. The key stage has been found to be the conditioning step where precautions must be taken to ensure that plutonium-containing precipitates and non-extractable plutonium are not formed. Consideration has also been given to treatment of the americium containing raffinates from a high acid TBP extraction and some methods have been investigated. A range of simple washing experiments have been carried out in order to compare the process with incineration/pyrolysis

Plutonium metal preparation and purification at Los Alamos, 1984

International Nuclear Information System (INIS)

Christensen, D.C.; Williams, J.D.; McNeese, J.A.; Fife, K.W.

1984-01-01

Plutonium metal preparation and purification are well established at Los Alamos. Metal is prepared by calcothermic reduction of both PuF 4 and PuO 2 . Metal is purified by halide slagging, casting, and electrorefining. The product from the production sequence is ultrapure plutonium metal. All of the processes involve high temperature operation and all but casting involve molten salt media. Development efforts are fourfold: (1) recover plutonium values from residues; (2) reduce residue generation through process improvements and changes; (3) recycle of reagents, and (4) optimize and integrate all processes into a close-loop system. Plutonium residues are comprised of oxides, chlorides, colloidal metal suspensions, and impure metal heels. Pyrochemical recovery techniques are under development to address each residue. In addition, we are looking back at each residue generation step and are making process changes to reduce plutonium content in each residue. Reagent salt is the principle media used in pyrochemical processing. The regeneration and recycle of these reagents will both reduce our waste handling and operating expense. The fourth area, process optimization, involves both existing processes and new process developments. A status of efforts in all four of these areas will be summarized

Plutonium immobilization program - Cold pour Phase 1 test results

International Nuclear Information System (INIS)

Hamilton, L.

2000-01-01

The Plutonium Immobilization Project will disposition excess weapons grade plutonium. It uses the can-in-canister approach that involves placing plutonium-ceramic pucks in sealed cans that are then placed into Defense Waste Processing Facility canisters. These canisters are subsequently filled with high-level radioactive waste glass. This process puts the plutonium in a stable form and makes it unattractive for reuse. A cold (non-radioactive) glass pour program was performed to develop and verify the baseline design for the canister and internal hardware. This paper describes the Phase 1 scoping test results

Plutonium Immobilization Program - Cold pour Phase 1 test results

International Nuclear Information System (INIS)

Hamilton, L.

2000-01-01

The Plutonium Immobilization Project will disposition excess weapons grade plutonium. It uses the can-in-canister approach that involves placing plutonium-ceramic pucks in sealed cans that are then placed into Defense Waste Processing Facility canisters. These canisters are subsequently filled with high-level radioactive waste glass. This process puts the plutonium in a stable form and makes it unattractive for reuse. A cold (non-radioactive) glass pour program was performed to develop and verify the baseline design for the canister and internal hardware. This paper describes the Phase 1 scoping test results

THE DEACTIVATION, DECONTAMINATION AND DECOMMISSIONING OF THE PLUTONIUM FINISHING PLANT, A FORMER PLUTONIUM PROCESSING FACILITY AT DOE'S HANFORD SITE

International Nuclear Information System (INIS)

CHARBONEAU, S.L.

2006-01-01

The Plutonium Finishing Plant (PFP) was constructed as part of the Manhattan Project during World War II. The Manhattan Project was developed to usher in the use of nuclear weapons to end the war. The primary mission of the PFP was to provide plutonium used as special nuclear material (SNM) for fabrication of nuclear devices for the war effort. Subsequent to the end of World War II, the PFP's mission expanded to support the Cold War effort through plutonium production during the nuclear arms race and later the processing of fuel grade mixed plutonium-uranium oxide to support DOE's breeder reactor program. In October 1990, at the close of the production mission for PFP, a shutdown order was prepared by the Department of Energy (DOE) in Washington,; DC--and issued to the Richland DOE field office. Subsequent to the shutdown order, a team from the Defense Nuclear Facilities Safety Board (DNFSB) analyzed the hazards at PFP associated with the continued storage of certain forms of plutonium solutions and solids. The assessment identified many discrete actions that were required to stabilize the different plutonium forms into stable form and repackage the material in high integrity containers. These actions were technically complicated and completed as part of the PFP nuclear material stabilization project between 1995 and early 2005. The completion of the stabilization project was a necessary first step in deactivating PFP. During stabilization, DOE entered into negotiations with the U.S. Environmental Protection Agency (EPA) and the State of Washington and established milestones for the Deactivation and Decommissioning (DandD) of the PFP. The DOE and its contractor, Fluor Hanford (Fluor), have made great progress in deactivating, decontaminating and decommissioning the PFP at the Hanford Site as detailed in this paper. Background information covering the PFP DandD effort includes descriptions of negotiations with the State of Washington concerning consent

Nondestructive assay of plutonium residue in horizontal storage tanks

International Nuclear Information System (INIS)

Marsh, S.F.

1985-01-01

Aqueous plutonium recovery and purification processes often involve the temporary storage of plutonium solutions in holding tanks. Because plutonium is known to precipitate from aqueous solutions under certain conditions, there is a continuing need to assay emptied tanks for plutonium residue. A portable gamma spectrometer system, specifically designed for this purpose, provides rapid assay of such plutonium residues in horizontal storage tanks. A means is thus available for the nondestructive analysis of these tanks on a regular schedule to ensure that significant deposits of plutonium are not allowed to accumulate. 5 figs

Analysis of civilian processing programs in reduction of excess separated plutonium and high-enriched uranium

International Nuclear Information System (INIS)

Persiani, P.J.

1995-01-01

The purpose of this preliminary investigation is to explore alternatives and strategies aimed at the gradual reduction of the excess inventories of separated plutonium and high-enriched uranium (HEU) in the civilian nuclear power industry. The study attempts to establish a technical and economic basis to assist in the formation of alternative approaches consistent with nonproliferation and safeguards concerns. The analysis addresses several options in reducing the excess separated plutonium and HEU, and the consequences on nonproliferation and safeguards policy assessments resulting from the interacting synergistic effects between fuel cycle processes and isotopic signatures of nuclear materials

Status summary of chemical processing development in plutonium-238 supply program

Energy Technology Data Exchange (ETDEWEB)

Collins, Emory D. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Benker, Dennis [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Wham, Robert M. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); DePaoli, David W. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Delmau, Laetitia Helene [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Sherman, Steven R. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States)

2017-10-01

This document summarizes the status of development of chemical processing in the Plutonium-238 Supply Program (PSP) near the end of Demonstration 1. The objective of the PSP is “to develop, demonstrate, and document a production process that meets program objectives and to prepare for its operation” (Frazier et al. 2016). Success in the effort includes establishing capability using the current infrastructure to produce Np targets for irradiation in Department of Energy research reactors, chemically processing the irradiated targets to separate and purify the produced Pu and transferring the PuO₂ product to Los Alamos National Laboratory (LANL) at an average rate of 1.5 kg/y.

Impact of ADTT concepts on the management of global plutonium inventories

International Nuclear Information System (INIS)

Davidson, J.W.; Krakowski, R.A.; Arthur, E.D.

1996-01-01

The impact of a number of current and future nuclear systems on global plutonium inventories is assessed under realistic forecasts of nuclear power growth. Advanced systems, such as those employing Accelerator Driven Transmutation Technologies (ADTT) and liquid metal reactors, show significant promise for meeting future plutonium management needs. These analyses also indicate requirements for a higher level of detail in the nuclear fuel cycle model and for development of a metric to more quantitatively assess the proliferation risk of plutonium arising from the civilian fuel cycle

Safeguarding the Plutonium Fuel Cycle

International Nuclear Information System (INIS)

Johnson, S.J.; Lockwood, D.

2013-01-01

In developing a Safeguards Approach for a plutonium process facility, two general diversion and misuse scenarios must be addressed: 1) Unreported batches of undeclared nuclear material being processed through the plant and bypassing the accountancy measurement points, and 2) The operator removing plutonium at a rate that cannot be detected with confidence due to measurement uncertainties. This paper will look at the implementation of international safeguards at plutonium fuel cycle facilities in light of past lessons learned and current safeguards approaches. It will then discuss technical areas which are currently being addressed as future tools to improve on the efficiency of safeguards implementation, while maintaining its effectiveness. The discussion of new improvements will include: safeguards by design (SBD), process monitoring (PM), measurement and monitoring equipment, and data management. The paper is illustrated with the implementation of international safeguards at the Rokkasho Reprocessing Plant in Japan and its accountancy structure is detailed. The paper is followed by the slides of the presentation

Determination of plutonium in pure plutonium nitrate solutions - Gravimetric method

International Nuclear Information System (INIS)

1987-01-01

This International Standard specifies a precise and accurate gravimetric method for determining the concentration of plutonium in pure plutonium nitrate solutions and reference solutions, containing between 100 and 300 g of plutonium per litre, in a nitric acid medium. The weighed portion of the plutonium nitrate is treated with sulfuric acid and evaporated to dryness. The plutonium sulfate is decomposed and formed to oxide by heating in air. The oxide is ignited in air at 1200 to 1250 deg. C and weighed as stoichiometric plutonium dioxide, which is stable and non-hygroscopic

Remote handling in the Plutonium Immobilization Project: Plutonium conversion and first stage immobilization

International Nuclear Information System (INIS)

Brault, J.R.

2000-01-01

Since the break up of the Soviet Union at the end of the Cold War, the United States and Russia have been negotiating ways to reduce their nuclear stockpiles. Economics is one of the reasons behind this, but another important reason is safeguarding these materials from unstable organizations and countries. With the downsizing of the nuclear stockpiles, large quantities of plutonium are being declared excess and must be safely disposed of. The Savannah River Site (SRS) has been selected as the site where the immobilization facility will be located. Conceptual design and process development commenced in 1998. SRS will immobilize excess plutonium in a ceramic waste form and encapsulate it in vitrified high level waste in the Defense Waste Processing Facility (DWPF) canister. These canisters will then be interred in the national repository at Yucca Mountain, New Mexico. The facility is divided into three distinct operating areas: Plutonium Conversion, First Stage Immobilization, and Second Stage Immobilization. This paper will discuss the first two operations

Plutonium working group report on environmental, safety and health vulnerabilities associated with the Department's plutonium storage. Volume I: Summary

International Nuclear Information System (INIS)

1994-11-01

At the conclusion of the Cold War, the Department of Energy (DOE) stopped plutonium processing for nuclear weapons production. Facilities used for that purpose now hold significant quantities of plutonium in various forms. Unless properly stored and handled, plutonium can present environment, safety and health (ES ampersand H) hazards. Improperly stored plutonium poses a variety of hazards. When containers or packaging fail to fully protect plutonium metal from exposure to air, oxidation can occur and cause packaging failures and personnel contamination. Contamination can also result when plutonium solutions leak from bottles, tanks or piping. Plutonium in the form of scrap or residues generated by weapons production are often very corrosive, chemically reactive and difficult to contain. Buildings and equipment that are aging, poorly maintained or of obsolete design contribute to the overall problem. Inadvertent accumulations of plutonium of any form in sufficient quantities within facilities can result in nuclear criticality events that could emit large amounts of radiation locally. Contamination events and precursors of criticality events are causing safety and health concerns for workers at the Department's plutonium facilities. Contamination events also potentially threaten the public and the surrounding environment

Search for plutonium salt deposits in the plutonium extraction batteries of the Marcoule plant (1963); Recherche de depots de sels de plutonium dans les batteries d'extraction du plutonium de l'usine de Marcoule (1963)

Energy Technology Data Exchange (ETDEWEB)

Bouzigues, H; Reneaud, J M [Commissariat a l' Energie Atomique, Centre de Production de Plutonium, Marcoule (France). Centre d' Etudes Nucleaires

1963-07-01

This report describes a method and a special apparatus making it possible to detach the insoluble plutonium salt deposits in the extraction chain of an irradiated fuel treatment plant. The process chosen allows the detection, in the extraction batteries or in the highly active chemical engineering equipment, of plutonium quantities of a few grains. After four years operation it has been impossible to detect measurable quantities of plutonium in any part of the extraction chain. The results have been confirmed by visual examinations carried out with a specially constructed endoscope. (authors) [French] Ce rapport decrit une methode et un montage special permettant de detacher les accumulations de sels de plutonium insolubles dans les chaines d'extraction d'une usine de traitement de combustible irradie. Le procede retenu permet de reperer, dans des batteries d'extraction ou dans l'appareillage de genie chimique fortement actif, des masses de plutonium de quelques grammes. Apres quatre annees de fonctionnement, il n'a pas ete possible de deceler des quantites ponderables de plutonium en aucun endroit de la chaine d'extraction. Ces resultats ont ete confirmes par les examens visuels effectues a l'aide d'un endoscope concu specialement pour cet usage. (auteurs)

Systems Analysis of an Advanced Nuclear Fuel Cycle Based on a Modified UREX+3c Process

International Nuclear Information System (INIS)

Johnson, E.R.; Best, R.E.

2009-01-01

The research described in this report was performed under a grant from the U.S. Department of Energy (DOE) to describe and compare the merits of two advanced alternative nuclear fuel cycles -- named by this study as the 'UREX+3c fuel cycle' and the 'Alternative Fuel Cycle' (AFC). Both fuel cycles were assumed to support 100 1,000 MWe light water reactor (LWR) nuclear power plants operating over the period 2020 through 2100, and the fast reactors (FRs) necessary to burn the plutonium and minor actinides generated by the LWRs. Reprocessing in both fuel cycles is assumed to be based on the UREX+3c process reported in earlier work by the DOE. Conceptually, the UREX+3c process provides nearly complete separation of the various components of spent nuclear fuel in order to enable recycle of reusable nuclear materials, and the storage, conversion, transmutation and/or disposal of other recovered components. Output of the process contains substantially all of the plutonium, which is recovered as a 5:1 uranium/plutonium mixture, in order to discourage plutonium diversion. Mixed oxide (MOX) fuel for recycle in LWRs is made using this 5:1 U/Pu mixture plus appropriate makeup uranium. A second process output contains all of the recovered uranium except the uranium in the 5:1 U/Pu mixture. The several other process outputs are various waste streams, including a stream of minor actinides that are stored until they are consumed in future FRs. For this study, the UREX+3c fuel cycle is assumed to recycle only the 5:1 U/Pu mixture to be used in LWR MOX fuel and to use depleted uranium (tails) for the makeup uranium. This fuel cycle is assumed not to use the recovered uranium output stream but to discard it instead. On the other hand, the AFC is assumed to recycle both the 5:1 U/Pu mixture and all of the recovered uranium. In this case, the recovered uranium is reenriched with the level of enrichment being determined by the amount of recovered plutonium and the combined amount of the

Systems Analysis of an Advanced Nuclear Fuel Cycle Based on a Modified UREX+3c Process

Energy Technology Data Exchange (ETDEWEB)

E. R. Johnson; R. E. Best

2009-12-28

The research described in this report was performed under a grant from the U.S. Department of Energy (DOE) to describe and compare the merits of two advanced alternative nuclear fuel cycles -- named by this study as the “UREX+3c fuel cycle” and the “Alternative Fuel Cycle” (AFC). Both fuel cycles were assumed to support 100 1,000 MWe light water reactor (LWR) nuclear power plants operating over the period 2020 through 2100, and the fast reactors (FRs) necessary to burn the plutonium and minor actinides generated by the LWRs. Reprocessing in both fuel cycles is assumed to be based on the UREX+3c process reported in earlier work by the DOE. Conceptually, the UREX+3c process provides nearly complete separation of the various components of spent nuclear fuel in order to enable recycle of reusable nuclear materials, and the storage, conversion, transmutation and/or disposal of other recovered components. Output of the process contains substantially all of the plutonium, which is recovered as a 5:1 uranium/plutonium mixture, in order to discourage plutonium diversion. Mixed oxide (MOX) fuel for recycle in LWRs is made using this 5:1 U/Pu mixture plus appropriate makeup uranium. A second process output contains all of the recovered uranium except the uranium in the 5:1 U/Pu mixture. The several other process outputs are various waste streams, including a stream of minor actinides that are stored until they are consumed in future FRs. For this study, the UREX+3c fuel cycle is assumed to recycle only the 5:1 U/Pu mixture to be used in LWR MOX fuel and to use depleted uranium (tails) for the makeup uranium. This fuel cycle is assumed not to use the recovered uranium output stream but to discard it instead. On the other hand, the AFC is assumed to recycle both the 5:1 U/Pu mixture and all of the recovered uranium. In this case, the recovered uranium is reenriched with the level of enrichment being determined by the amount of recovered plutonium and the combined amount

Solvent extraction process development for high plutonium fuel cycles

Energy Technology Data Exchange (ETDEWEB)

Anil Kumar, R; Selvaraj, P G; Natarajan, R; Raman, V R [Reprocessing Group, Indira Gandhi Centre for Atomic Research, Kalpakkam (India)

1994-06-01

The purification of high plutonium bearing irradiated fuels using 30% TBP in dodecane diluent requires precise determination of concentration profiles during steady state, transient and process upset conditions. Mathematical models have been developed and a computer code is in use for determining Pu-U concentration profiles in a solvent extraction equipment in a typical reprocessing plant. The process parameters have been optimised for recovery of U and Pu and decontamination from the fission products. This computer code is used to analyse the extraction flow sheets of fuels of two typical Pu-U compositions encountered in Indian fast breeder programme. The analysis include the effect of uncertainty in equilibrium condition prediction by the model and the variation of flows of streams during plant operation. The studies highlight the margin available to avoid second organic phase formation and adjustments required in the process flowsheet. (author). 7 refs., 7 figs., 2 tabs.

Experimental Studies on Plutonium Kinetics in Marine Biota

International Nuclear Information System (INIS)

Fowler, S.; Heyraud, M.; Beasley, T.M.

1976-01-01

Laboratory experiments were undertaken to measure plutonium flux through marine organisms and to clarify the pathways by which this important element is cycled in the marine environment. The use of a specially prepared isotope, plutonium-237, allowed measurements to be made with standard Nal(Tl) scintillation techniques. Mussels, shrimp and worms were allowed to accumulate plutonium-237 from sea water for up to 25 days. Accumulation by shrimp was relatively slow and the degree of uptake was strongly influenced by moulting. Cast moults contained large fractions of the shrimps ' plutonium content, indicating the high affinity of plutonium for surface areas. Only small amounts of the isotope in the moult are lost to water; hence, moulting is considered to be an important biological parameter in the biogeochemical cycling of plutonium. Mussels attained higher concentration factors than shrimp with most of the accumulated isotope (> 80%) located in the shell. Byssus threads often contained large fractions of the mussels' plutonium-237 content and reached concentration factors as high as 4100. Worms readily accumulated plutonium-237 in either the +4 or +6 state, reaching concentration factors of approximately 200, Retention studies indicated a relatively slow loss of plutonium-237 from all animals studied. In the case of mussels, a computed half-time for a large fraction of the animals plutonium content was of the order of 2 years. The more rapid loss from shrimp (Tb 1/2 = 1.5 months) was due principally to the large fraction of plutonium lost at moult. Food chain studies with shrimp indicated that tissue build-up via plutonium ingestion would be a slow process. Total excretion was not entirely a result of passing contaminated food through the gut; approximately 15% of the ingested plutonium was removed from the contaminated food and subsequently excreted by processes other than defaecation of labelled food. Ratios of four different plutonium isotopes used in

Experimental studies on plutonium kinetics in marine biota

International Nuclear Information System (INIS)

Fowler, S.; Heyraud, M.; Beasley, T.M.

1975-01-01

Laboratory experiments were undertaken to measure plutonium flux through marine organisms and to clarify the pathways by which this important element is cycled in the marine environment. The use of a specially prepared isotope, plutonium-237, allowed measurements to be made with standard NaI(Tl) scintillation techniques. Mussels, shrimp and worms were allowed to accumulate plutonium-237 from seawater for up to 25 days. Accumulation by shrimp was relatively slow and the degree of uptake was strongly influenced by moulting. Cast moults contained large fractions of the shrimps' plutonium content, indicating the high affinity of plutonium for surface areas. Only small amounts of the isotope in the moult are lost to water; hence, moulting is considered to be an important biological parameter in the biogeochemical cycling of plutonium. Mussels attained higher concentration factors than shrimp with most of the accumulated isotope (>80%) located in the shell. Byssus threads often contained large fractions of the mussels' plutonium-237 content and reached concentration factors as high as 4100. Worms readily accumulated plutonium-237 in either the +4 or +6 state, reaching concentration factors of approximately 200. Retention studies indicated a relatively slow loss of plutonium-237 from all animals studied. In the case of mussels, a computed half-time for a large fraction of the animals' plutonium content was of the order of 2 years. The more rapid loss from shrimp (Tbsub(1/2)=1.5 months) was due principally to the large fraction of plutonium lost at moult. Food chain studies with shrimp indicated that tissue build-up via plutonium ingestion would be a slow process. Total excretion was not entirely a result of passing contaminated food through the gut; approximately 15% of the ingested plutonium was removed from the contaminated food and subsequently excreted by processes other than defaecation of labelled food. Ratios of four different plutonium isotopes used in the

Plutonium-236 traces determination in plutonium-238 by α spectrometry

International Nuclear Information System (INIS)

Acena, M.L.; Pottier, R.; Berger, R.

1969-01-01

Two methods are described in this report for the determination of plutonium-236 traces in plutonium-238 by a spectrometry using semi-conductor detectors. The first method involves a direct comparison of the areas under the peaks of the α spectra of plutonium-236 and plutonium-238. The electrolytic preparation of the sources is carried out after preliminary purification of the plutonium. The second method makes it possible to determine the 236 Pu/ 238 Pu ratio by comparing the areas of the α peaks of uranium-232 and uranium-234, which are the decay products of the two plutonium isotopes respectively. The uranium in the source, also deposited by electrolysis, is separated from a 1 mg amount of plutonium either by a T.L.A. extraction, or by the use of ion-exchange resins. The report ends with a discussion of the results obtained with plutonium of two different origins. (authors) [fr

Direct reduction of plutonium from dicesium hexachloroplutonate

International Nuclear Information System (INIS)

Averill, W.A.; Boyd, T.E.

1991-01-01

The Rocky Flats Plant produces dicesium hexachloroplutonate (DCHP) primarily as a reagent in the molten salt extraction of americium from plutonium metal. DCHP is precipitated from aqueous chloride solutions derived from the leaching of process residues with a high degree of selectivity. DCHP is a chloride salt of plutonium, while the traditional aqueous precipitate is a hydrated oxide. Plutonium metal preparation from the oxide involves either the conversion of oxide to a halide followed by metallothermic reduction or direct reduction of the oxide using a flux. Either method generates at least three times as much radioactively contaminated waste as metal produced. Plutonium concentration by DCHP precipitation, however, produces a chloride salt that can be reduced using calcium metal at a temperature of approximately 1000K. In this paper the advantages and limitations of this process are discussed

Geomorphology of plutonium in the Northern Rio Grande

Energy Technology Data Exchange (ETDEWEB)

Graf, W.L. [Arizona Univ., Tempe, AZ (United States). Dept., of Geography

1993-03-01

Nearly all of the plutonium in the natural environment of the Northern Rio Grande is associated with soils and sediment, and river processes account for most of the mobility of these materials. A composite regional budget for plutonium based on multi-decadal averages for sediment and plutonium movement shows that 90 percent of the plutonium moving into the system is from atmospheric fallout. The remaining 10 percent is from releases at Los Alamos. Annual variation in plutonium flux and storage exceeds 100 percent. The contribution to the plutonium budget from Los Alamos is associated with relatively coarse sediment which often behaves as bedload in the Rio Grande. Infusion of these materials into the main stream were largest in 1951, 1952, 1957, and 1968. Because of the schedule of delivery of plutonium to Los Alamos for experimentation and weapons manufacturing, the latter two years are probably the most important. Although the Los Alamos contribution to the entire plutonium budget was relatively small, in these four critical years it constituted 71--86 percent of the plutonium in bedload immediately downstream from Otowi.

Geomorphology of plutonium in the Northern Rio Grande

International Nuclear Information System (INIS)

Graf, W.L.

1993-03-01

Nearly all of the plutonium in the natural environment of the Northern Rio Grande is associated with soils and sediment, and river processes account for most of the mobility of these materials. A composite regional budget for plutonium based on multi-decadal averages for sediment and plutonium movement shows that 90 percent of the plutonium moving into the system is from atmospheric fallout. The remaining 10 percent is from releases at Los Alamos. Annual variation in plutonium flux and storage exceeds 100 percent. The contribution to the plutonium budget from Los Alamos is associated with relatively coarse sediment which often behaves as bedload in the Rio Grande. Infusion of these materials into the main stream were largest in 1951, 1952, 1957, and 1968. Because of the schedule of delivery of plutonium to Los Alamos for experimentation and weapons manufacturing, the latter two years are probably the most important. Although the Los Alamos contribution to the entire plutonium budget was relatively small, in these four critical years it constituted 71--86 percent of the plutonium in bedload immediately downstream from Otowi

Plutonium controversy

International Nuclear Information System (INIS)

Gofman, J.W.

1976-01-01

If the world chooses to seek a solution to the energy dilemma through nuclear energy, the element plutonium will become an article of commerce to be handled in quantities of thousands of tonnes annually. Plutonium is a uniquely potent inhalation carcinogen, the potential induction of lung cancer dwarfing other possible toxic effects. For reasons to be presented here, it is the author's opinion that plutonium's carcinogenicity has been very seriously underestimated. If one couples the corrected carcinogenicity with the probable degree of industrial containment of the plutonium, it appears that the commercialization of a plutonium-based energy economy is not an acceptable option for society. Sagan's statement that ''the experience of 30 years supports the contention that plutonium can be used safely'' is manifestly indefensible. No meaningful epidemiological study of plutonium-exposed workers for that 30-year period has ever been done. Since thousands of those possibly exposed have left the industry and are not even available to follow-up, it is doubtful that any meaningful study of ''the experience of 30 years'' will ever be accomplished

Plutonium working group report on environmental, safety and health vulnerabilities associated with the Department's plutonium storage. Volume 2, Appendix A: Process and protocol

International Nuclear Information System (INIS)

1994-09-01

This appendix contains documentation prepared by the Plutonium ES and H Vulnerability Working Group for conducting the Plutonium ES and H Vulnerability Assessment and training the assessment teams. It has the following five parts. (1) The Project Plan describes the genesis of the project, sets forth the goals, objectives and scope, provides definitions, the projected schedule, and elements of protocol. (2) The Assessment Plan provides a detailed methodology necessary to guide the many professionals who have been recruited to conduct the DOE-wide assessment. It provides guidance on which types and forms of plutonium are to be considered within the scope of the assessment, and lays out the assessment methodology to be used. (3) The memorandum from the Project to Operations Office Managers provides the protocol and direction for participation in the assessment by external stakeholders and members of the public; and the guidance for the physical inspection of plutonium materials in storage. (4) The memorandum from the Project to the assessment teams provides guidance for vulnerability screening criteria, vulnerability evaluation and prioritization process, and vulnerability quantification for prioritization. (5) The Team Training manual was used at the training session held in Colorado Springs on April 19--21, 1994 for all members of the Working Group Assessment Teams and for the leaders of the Site Assessment Teams. The goal was to provide the same training to all of the individuals who would be conducting the assessments, and thereby provide consistency in the conduct of the assessments and uniformity in reporting of the results. The training manual in Section A.5 includes supplemental material provided to the attendees after the meeting

Preparation of hexavalent plutonium and its determination in the presence of tetravalent plutonium; Preparation de plutonium hexavalent et dosage en presence de plutonium tetravalent

Energy Technology Data Exchange (ETDEWEB)

Corpel, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires; Corpel, J [Institut du Radium, 75 - Paris (France)

1958-07-01

In order to study the eventual reduction of plutonium from the VI-valent state to the IV-valent state, in sulphuric medium, under the influence of its own {alpha} radiation or of the {gamma}-rays from a cobalt-60 source, we have developed a method for preparing pure hexavalent plutonium and two methods for determining solutions containing tetravalent and hexavalent plutonium simultaneously. Hexavalent plutonium was prepared by anodic oxidation at a platinum electrode. Study of the oxidation yield as a function of various factors has made it possible to define experimental conditions giving complete oxidation. For concentrations in total plutonium greater than 1.5 x 10{sup -3} M, determination of the two valencies IV and VI was carried out by spectrophotometry at two wavelengths. For lower concentrations, the determination was done by counting, after separation of the tetravalent plutonium in the form of fluoride in the presence of a carrier. (author) [French] Afin d'etudier l'eventuelle reduction du plutonium de l'etat de valence VI a l'etat de valence IV, en milieu sulfurique sous l'influence de son propre rayonnement {alpha} ou des rayons {gamma} d'une source de cobalt-60, nous avons mis au point une methode de preparation de plutonium hexavalent pur et deux methodes de dosage des solutions contenant simultanement du plutonium tetravalent et du plutonium hexavalent. Nous avons prepare le plutonium hexavalent par oxydation anodique au contact d'une electrode de platine. L'etude de rendement de l'oxydation en fonction des divers facteurs nous a permis de definir des conditions experimentales donnant une oxydation complete. Pour des concentrations en plutonium total superieures a 1,5.10{sup -3} M, le dosage des deux valences IV et VI a ete realise par spectrophotometrie a deux longueurs d'onde. Pour des concentrations inferieures, le dosage a ete effectue par comptage apres separation du plutonium tetravalent sous la forme du fluorure en presence d'un entraineur

Plutonium in nature

International Nuclear Information System (INIS)

Madic, C.

1994-01-01

Plutonium in nature comes from natural sources and anthropogenic ones. Plutonium at the earth surface comes principally from anthropogenic sources. It is easily detectable in environment. The plutonium behaviour in environment is complex. It seems necessary for the future to reduce releases in environment, to improve predictive models of plutonium behaviour in geosphere, to precise biological impact of anthropogenic plutonium releases

Advanced pyrochemical technologies for minimizing nuclear waste

International Nuclear Information System (INIS)

Bronson, M.C.; Dodson, K.E.; Riley, D.C.

1994-01-01

The Department of Energy (DOE) is seeking to reduce the size of the current nuclear weapons complex and consequently minimize operating costs. To meet this DOE objective, the national laboratories have been asked to develop advanced technologies that take uranium and plutonium, from retired weapons and prepare it for new weapons, long-term storage, and/or final disposition. Current pyrochemical processes generate residue salts and ceramic wastes that require aqueous processing to remove and recover the actinides. However, the aqueous treatment of these residues generates an estimated 100 liters of acidic transuranic (TRU) waste per kilogram of plutonium in the residue. Lawrence Livermore National Laboratory (LLNL) is developing pyrochemical techniques to eliminate, minimize, or more efficiently treat these residue streams. This paper will present technologies being developed at LLNL on advanced materials for actinide containment, reactors that minimize residues, and pyrochemical processes that remove actinides from waste salts

Plutonium Contaminated Materials Working Party development programme

International Nuclear Information System (INIS)

Higson, S.G.

1985-01-01

The broad objectives of the programme are to develop and assess: (a) techniques for the minimisation, treatment and encapsulation of solid PCM; (b) techniques for the measurement of plutonium in encapsulated and unencapsulated PCM; and (c) advanced treatments for alpha bearing liquid wastes, in order to provide information on their waste management implications. Development has been carried out in eight areas: (a) reduction of arisings; (b) plutonium measurement; (c) decommissioning and non-combustible PCM treatments; (d) washing; (e) PCM immobilisation; (f) liquid effluent treatment; (g) sorting and packaging; and (h) engineering objectives. The work is reported. (author)

SEPARATION OF PLUTONIUM

Science.gov (United States)

Maddock, A.G.; Smith, F.

1959-08-25

A method is described for separating plutonium from uranium and fission products by treating a nitrate solution of fission products, uranium, and hexavalent plutonium with a relatively water-insoluble fluoride to adsorb fission products on the fluoride, treating the residual solution with a reducing agent for plutonium to reduce its valence to four and less, treating the reduced plutonium solution with a relatively insoluble fluoride to adsorb the plutonium on the fluoride, removing the solution, and subsequently treating the fluoride with its adsorbed plutonium with a concentrated aqueous solution of at least one of a group consisting of aluminum nitrate, ferric nitrate, and manganous nitrate to remove the plutonium from the fluoride.

1982 Annual Status Report Plutonium Fuels and Actinide Programme

International Nuclear Information System (INIS)

Lindner, R.

1983-01-01

The programme of the Transuranium Institute has long included work on advanced fuels for fast breeder reactors. Study of the swelling of carbide and nitride fuels is now nearing completion, the retention of fission gases in bubbles of different sizes in the fuel having been quantified as function of burn-up and temperature. An important step forward has been achieved in the studies of the Equation of State of Nuclear Fuels up to 5000 K. Formation of some of the less abundant isotopes in PWR fuel has been determined experimentally. Aerosol formation during the fabrication of plutonium containing fuels, part of the activity Safe Handling of Plutonium Fuel has been studied. Head-End Processing of carbide fuels has continued experiments with high burn up mixed carbides. In the field of actinide research the preparation and characterisation of pure specimens is carried out. Effect of actinides on the properties of waste glasses is investigated

Critical and subcritical parameters of the system simulating plutonium metal dissolution

International Nuclear Information System (INIS)

Vasilev, Yury Yu.; Ryazanov, Boris G.; Sviridov, Victor I.; Mozhayeva, Lubov I.

2003-01-01

Dissolution of plutonium metal was simulated using the Monte Carlo computer code to calculate criticality safety limits for the process. Calculations were made for the constant masses of plutonium charged to the dissolving vessel considering distribution of plutonium in metal and solution phases. Critical parameters and limits were calculated as a function of dissolving vessel volume and plutonium metal mass. 240 Pu content was assumed to be from 0% to 10% (mass). Critical parameters were evaluated for the system with a water reflector. Results of this paper may be used in the designing process equipment for plutonium metal dissolution. (author)

Tracing discharges of plutonium and technetium from nuclear processing plants by ultra-sensitive accelerator mass spectrometry

International Nuclear Information System (INIS)

Fifield, L.K.; Hausladen, P.A.; Cresswell, R.G.; Di Tada, M.L.; Day, J.P.; Carling, R.S.; Oughton, D.H.

1999-01-01

Historical discharges of plutonium from the Russian nuclear processing plant at Mayak in the Urals have been traced in sediments, soils and river water using ultra-sensitive detection of plutonium isotopes by accelerator mass spectrometry (AMS). Significant advantages of AMS over other techniques are its very high sensitivity. which is presently ∼10 6 atoms (1 μBq), and its ability to determine the 240 Pu/ 239 Pu ratio. The latter is a sensitive indicator of the source of the plutonium, being very low (1-2%) for weapons grade plutonium, and higher (∼ 20%) for plutonium from civil reactors or fallout from nuclear weapons testing. Since this ratio has changed significantly over the years of discharges from Mayak, a measurement can provide important information about the source of plutonium at a particular location. Similar measurements have been performed on samples from the Kara Sea which contains a graveyard of nuclear submarines from the former Soviet Union. AMS techniques have also been developed for detection of 99 Tc down to levels of a few femtograms. This isotope is one of the most prolific fission products and has a very long half-life of 220 ka. Hundreds of kg have been discharged from the nuclear reprocessing plant at Sellafield in the UK. While there may be public health issues associated with these discharges which can be addressed with AMS, these discharges may also constitute a valuable oceanographic tracer experiment in this climatically-important region of the world's oceans. Applications to date have included a human uptake study to assess long-term retention of 99 Tc in the body, and a survey of seaweeds from northern Europe to establish a baseline for a future oceanographic study

Measurements of plutonium in environmental samples

International Nuclear Information System (INIS)

D'Alberti, F.; Risposi, L.

1996-01-01

Within the activities connected with the start up of the PETRA Laboratory (Processo per l'Estrazione di Terre Rare ed Attinidi, i.e. process for extraction of rare earths and actinides), the Radiation Protection Unit of the J.R.C.-Ispra has carried out a well planned set of experimental measurements aimed at evaluating the zero point of the isotopes of plutonium in environmental samples by alfa spectrometry. After the International Moratorium in 1963, no release of plutonium has occurred in the environment apart from the burn up of SNAP 9A satellite in April 1964. Since then the plutonium concentration in air and in fallout samples has been continuously decreasing requiring, therefore, optimization of both instrumentation and experimental measurement procedures in order to obtain better sensibilities. In this work, the experimental methodology followed at the J.R.C.-Ispra for measurements of plutonium concentration in air, deposition and soil is described and the plutonium behaviour in these samples is reported and discussed starting from 1961

Measurements of plutonium in environmental samples

Energy Technology Data Exchange (ETDEWEB)

D' Alberti, F; Risposi, L [Instituto di Fisica Applicata, University of Milan, Milan (Italy)

1996-01-01

Within the activities connected with the start up of the PETRA Laboratory (Processo per l'Estrazione di Terre Rare ed Attinidi, i.e. process for extraction of rare earths and actinides), the Radiation Protection Unit of the J.R.C.-Ispra has carried out a well planned set of experimental measurements aimed at evaluating the zero point of the isotopes of plutonium in environmental samples by alfa spectrometry. After the International Moratorium in 1963, no release of plutonium has occurred in the environment apart from the burn up of SNAP 9A satellite in April 1964. Since then the plutonium concentration in air and in fallout samples has been continuously decreasing requiring, therefore, optimization of both instrumentation and experimental measurement procedures in order to obtain better sensibilities. In this work, the experimental methodology followed at the J.R.C.-Ispra for measurements of plutonium concentration in air, deposition and soil is described and the plutonium behaviour in these samples is reported and discussed starting from 1961.

Plutonium Finishing Plant (PFP) Final Safety Analysis Report (FSAR) [SEC 1 THRU 11

Energy Technology Data Exchange (ETDEWEB)

ULLAH, M K

2001-02-26

The Plutonium Finishing Plant (PFP) is located on the US Department of Energy (DOE) Hanford Site in south central Washington State. The DOE Richland Operations (DOE-RL) Project Hanford Management Contract (PHMC) is with Fluor Hanford Inc. (FH). Westinghouse Safety Management Systems (WSMS) provides management support to the PFP facility. Since 1991, the mission of the PFP has changed from plutonium material processing to preparation for decontamination and decommissioning (D and D). The PFP is in transition between its previous mission and the proposed D and D mission. The objective of the transition is to place the facility into a stable state for long-term storage of plutonium materials before final disposition of the facility. Accordingly, this update of the Final Safety Analysis Report (FSAR) reflects the current status of the buildings, equipment, and operations during this transition. The primary product of the PFP was plutonium metal in the form of 2.2-kg, cylindrical ingots called buttoms. Plutonium nitrate was one of several chemical compounds containing plutonium that were produced as an intermediate processing product. Plutonium recovery was performed at the Plutonium Reclamation Facility (PRF) and plutonium conversion (from a nitrate form to a metal form) was performed at the Remote Mechanical C (RMC) Line as the primary processes. Plutonium oxide was also produced at the Remote Mechanical A (RMA) Line. Plutonium processed at the PFP contained both weapons-grade and fuels-grade plutonium materials. The capability existed to process both weapons-grade and fuels-grade material through the PRF and only weapons-grade material through the RMC Line although fuels-grade material was processed through the line before 1984. Amounts of these materials exist in storage throughout the facility in various residual forms left from previous years of operations.

In-line measurement of plutonium and americium in mixed solutions

International Nuclear Information System (INIS)

Li, T.K.

1981-01-01

A solution assay instrument (SAI) has been developed at the Los Alamos National Laboratory and installed in the plutonium purification and americium recovery process area in the Los Alamos Plutonium Processing Facility. The instrument is designed for accurate, timely, and simultaneous nondestructive analysis of plutonium and americium in process solutions that have a wide range of concentrations and Am/Pu ratios. For a 25-mL sample, the assay precision is 5 g/L within a 2000-s count time

Flexible process options for the immobilisation of residues and wastes containing plutonium

International Nuclear Information System (INIS)

Stewart, M.W.A.; Moricca, S.A.; Day, R. A.; Begg, B. D.; Scales, C. R.; Maddrell, E. R.; Eilbeck, A. B.

2007-01-01

Residues and waste streams containing plutonium present unique technical, safety, regulatory, security, and socio-political challenges. In the UK these streams range from lightly plutonium contaminated materials (PCM) through to residue s resulting directly from Pu processing operations. In addition there are potentially stocks of Pu oxide powders whose future designation may be either a waste or an asset, due to their levels of contamination making their reuse uneconomic, or to changes in nuclear policy. While waste management routes exist for PCM, an immobilisation process is required for streams containing higher levels of Pu. Such a process is being developed by Nexia Solutions and ANSTO to treat and immobilise Pu waste and residues currently stored on the Sellafield site. The characteristics of these Pu waste streams are highly variable. The physical form of the Pu waste ranges from liquids, sludges, powders/granules, to solid components (e.g., test fuels), with the Pu present as an ion in solution, as a salt, metal, oxide or other compound. The chemistry of the Pu waste streams also varies considerably with a variety of impurities present in many waste streams. Furthermore, with fissile isotopes present, criticality is an issue during operations and in the store or repository. Safeguards and security concerns must be assessed and controlled. The process under development, by using a combination of tailored waste form chemistry combined with flexible process technology aims to develop a process line to handle a broad range of Pu waste streams. It aims to be capable of dealing with not only current arisings but those anticipated to arise as a result of future operations or policy changes. (authors)

Managing plutonium in Britain. Current options

International Nuclear Information System (INIS)

1998-01-01

This is the report of a two day meeting to discuss issues arising from the reprocessing of plutonium and production of mixed oxide nuclear fuels in Britain. It was held at Charney Manor, near Oxford, on June 25 and 26, 1998, and was attended by 35 participants, including government officials, scientists, policy analysts, representatives of interested NGO's, journalists, a Member of Parliament, and visiting representatives from the US and Irish governments. The topic of managing plutonium has been a consistent thread within ORG's work, and was the subject of one of our previous reports, CDR 12. This particular seminar arose out of discussions earlier in the year between Dr. Frank Barnaby and the Rt. Hon. Michael Meacher MP, Minister for the Environment. With important decisions about the management of plutonium in Britain pending, ORG undertook to hold a seminar at which all aspects of the subject could be aired. A number of on-going events formed the background to this initiative. The first was British Nuclear Fuels' [BNFL] application to the Environment Agency to commission a mixed oxide fuel [MOX] plant at Sellafield. The second was BNFL's application to vary radioactive discharge limits at Sellafield. Thirdly, a House of Lords Select Committee was in process of taking evidence, on the disposal of radioactive waste. Fourthly, the Royal Society, in a recent report entitled Management of Separated Plutonium, recommended that 'the Government should commission a comprehensive review... of the options for the management of plutonium'. Four formal presentations were made to the meeting, on the subjects of Britain's plutonium policy, commercial prospects for plutonium use, problems of plutonium accountancy, and the danger of nuclear terrorism, by experts from outside the nuclear industry. It was hoped that the industry's viewpoint would also be heard, and BNFL were invited to present a paper, but declined on the grounds that they were 'currently involved in a formal

Preconceptual design for separation of plutonium and gallium by ion exchange

International Nuclear Information System (INIS)

DeMuth, S.F.

1997-01-01

The disposition of plutonium from decommissioned nuclear weapons, by incorporation into commercial UO 2 -based nuclear reactor fuel, is a viable means to reduce the potential for theft of excess plutonium. This fuel, which would be a combination of plutonium oxide and uranium oxide, is referred to as a mixed oxide (MOX). Following power generation in commercial reactors with this fuel, the remaining plutonium would become mixed with highly radioactive fission products in a spent fuel assembly. The radioactivity, complex chemical composition, and large size of this spent fuel assembly, would make theft difficult with elaborate chemical processing required for plutonium recovery. In fabricating the MOX fuel, it is important to maintain current commercial fuel purity specifications. While impurities from the weapons plutonium may or may not have a detrimental affect on the fuel fabrication or fuel/cladding performance, certifying the effect as insignificant could be more costly than purification. Two primary concerns have been raised with regard to the gallium impurity: (1) gallium vaporization during fuel sintering may adversely affect the MOX fuel fabrication process, and (2) gallium vaporization during reactor operation may adversely affect the fuel cladding performance. Consequently, processes for the separation of plutonium from gallium are currently being developed and/or designed. In particular, two separation processes are being considered: (1) a developmental, potentially lower cost and lower waste, thermal vaporization process following PuO 2 powder preparation, and (2) an off-the-shelf, potentially higher cost and higher waste, aqueous-based ion exchange (IX) process. While it is planned to use the thermal vaporization process should its development prove successful, IX has been recommended as a backup process. This report presents a preconceptual design with material balances for separation of plutonium from gallium by IX

Plutonium oxide dissolution

International Nuclear Information System (INIS)

Gray, J.H.

1992-01-01

Several processing options for dissolving plutonium oxide (PuO 2 ) from high-fired materials have been studied. The scoping studies performed on these options were focused on PuO 2 typically generated by burning plutonium metal and PuO 2 produced during incineration of alpha contaminated waste. At least two processing options remain applicable for dissolving high-fired PuO 2 in canyon dissolvers. The options involve solid solution formation of PuO 2 With uranium oxide (UO 2 ) and alloying incinerator ash with aluminum. An oxidative dissolution process involving nitric acid solutions containing a strong oxidizing agent, such as cerium (IV), was neither proven nor rejected. This uncertainty was due to difficulty in regenerating cerium (IV) ions during dissolution. However, recent work on silver-catalyzed dissolution of PuO 2 with persulfate has demonstrated that persulfate ions regenerate silver (II). Use of persulfate to regenerate cerium (IV) or bismuth (V) ions during dissolution of PuO 2 materials may warrant further study

Erosional losses of fallout plutonium

International Nuclear Information System (INIS)

Foster, G.R.; Hakonson, T.E.

1987-01-01

Plutonium from fallout after atmospheric explosion of nuclear weapons in the 1950's and 1960s is being redistributed over the landscape by soil erosion and carried on sediment by streams to oceans. Erosion rates computed with the Universal Soil Loss Equation for more than 200,000 sample points on nonfederal land across the US were used to estimate plutonium removal rates by soil erosion. On the average, only about 4% of the eroded sediment reaches the outlet of a major river. The remaining sediment is deposited en route, and because deposition is a selective process, the sediment is enriched in fine particles having the highest concentration of plutonium because of the element's strong association with clay and silt-sized sediment. Estimated enrichment ratios, sediment delivery ratios, and erosion rates were used to estimate annual delivery of fallout plutonium. These estimates ranged from 0.002% of the initial fallout plutonium inventory for the Savannah River basin to 0.01% for the Columbia River basin, to 0.02% for the Hudson and Rio Grande River basins, to 0.08% for the Mississippi River basin. If the deposition of plutonium had been uniformly 1 mCi/km 2 , the estimated plutonium activity on suspended sediment would range from about 7 fCi/g of sediment of the Savannah River basin, to 9 fCi/g for the Mississippi River basin, to 12 fCi/g for the Hudson River basin, to 14 fCi/g for the Columbia and Rio Grande River basins. 45 references, 2 figures, 17 tables

Field test of plutonium and thorium contaminated clay soils from the Mound Site using the ACT*DE*CON Process

International Nuclear Information System (INIS)

Johnson, J.O.; Swift, N.A.; Church, R.H.; Neff, R.A.

1998-01-01

A treatability test was run during the summer and fall of 1997 to demonstrate the effectiveness of ACT*DE*CON for removing plutonium and thorium from the clay soils around Mound. ACT*DE*CON is a proprietary solution patented by Selentec. The process utilized a highly selective dissolution of the contaminants by the use of a chemical wash. The pilot scale process involved pretreatment of the soil in an attrition scrubber with ACT*DE*CON solution. This blended solution was then passed through a counter-current extraction chamber where additional contact with ACT*DE*CON solution occurred, followed by a rinse cycle. During this process sand was added to aid contact of the solution with the soil particles. The sand is removed during the rinse step and reused. The chelating agent is separated from the contaminant and recycled back into the process, along with the reverse osmosis permeate. The resulting solution can be further treated to concentrate the contaminant. Three different types of environmental soils were tested -- plutonium and thorium contaminated soils with the natural clay content, and plutonium contaminated soils with a high percentage of fine clay particles. The goal of these tests was to reduce the plutonium levels from several hundreds of pCi/g to between 25 and 75 pCi/g and the thorium from a couple hundred pCi/g to less than 5 pCi/g. The results of these four tests are presented along with a discussion of the operating parameters and the lessons learned relating to full scale implementation at Mound as well as other potential applications of this process

Los Alamos DP West Plutonium Facility decontamination project

International Nuclear Information System (INIS)

Garde, R.; Cox, E.J.; Valentine, A.M.

1982-01-01

The DP West Plutonium Facility operated by the Los Alamos National Laboratory, Los Alamos, New Mexico, was decontaminated between April 1978 and April 1981. The facility was constructed in 1944 to 1945 to produce plutonium metal and fabricate parts for nuclear weapons. It was continually used as a plutonium processing and research facility until mid-1978. Decontamination operations included dismantling and removing gloveboxes and conveyor tunnels; removing process systems, utilities, and exhaust ducts; and decontaminating all remaining surfaces. This report describes glovebox and conveyor tunnel separations, decontamination techniques, health and safety considerations, waste management procedures, and costs of the operation

Nondestructive analysis of plutonium contaminated soil

International Nuclear Information System (INIS)

Smith, H.E.; Taylor, L.H.

1977-01-01

Plutonium contaminated soil is currently being removed from a covered liquid waste disposal trench near the Pu Processing facility on the Hanford Project. This soil with the plutonium is being mined using remote techniques and equipment. The mined soil is being packaged for placement into retrievable storage, pending possible recovery. To meet the requirements of criticality safety and materials accountability, a nondestructive analysis program has been developed to determine the quantity of plutonium in each packing-storage container. This paper describes the total measurement program: equipment systems, calibration techniques, matrix assumption, instrument control program and a review of laboratory operating experience

Plutonium

International Nuclear Information System (INIS)

Anon.

1995-01-01

Plutonium, which was obtained and identified for the first time in 1941 by chemist Glenn Seaborg - through neutron irradiation of uranium 238 - is closely related to the history of nuclear energy. From the very beginning, because of the high radiotoxicity of plutonium, a tremendous amount of research work has been devoted to the study of the biological effects and the consequences on the environment. It can be said that plutonium is presently one of the elements, whose nuclear and physico-chemical characteristics are the best known. The first part of this issue is a survey of the knowledge acquired on the subject, which emphasizes the sanitary effects and transfer into the environment. Then the properties of plutonium related to energy generation are dealt with. Fissionable, like uranium 235, plutonium has proved a high-performance nuclear fuel. Originally used in breeder reactors, it is now being more and more widely recycled in light water reactors, in MOX fuel. Reprocessing, recycling and manufacturing of these new types of fuel, bound of become more and more widespread, are now part of a self-consistent series of operations, whose technical, economical, industrial and strategical aspects are reviewed. (author)

Learning more about plutonium

International Nuclear Information System (INIS)

2005-01-01

This document offers chemical, metallurgical and economical information on the plutonium, a hard white radioelement. It deals also on the plutonium formation in the earth, the plutonium use in the nuclear industry, the plutonium in the environment and the plutonium toxicity. (A.L.B.)

SEPARATION OF URANIUM, PLUTONIUM, AND FISSION PRODUCTS

Science.gov (United States)

Spence, R.; Lister, M.W.

1958-12-16

Uranium and plutonium can be separated from neutron-lrradiated uranium by a process consisting of dissolvlng the lrradiated material in nitric acid, saturating the solution with a nitrate salt such as ammonium nitrate, rendering the solution substantially neutral with a base such as ammonia, adding a reducing agent such as hydroxylamine to change plutonium to the trivalent state, treating the solution with a substantially water immiscible organic solvent such as dibutoxy diethylether to selectively extract the uranium, maklng the residual aqueous solutlon acid with nitric acid, adding an oxidizing agent such as ammonlum bromate to oxidize the plutonium to the hexavalent state, and selectlvely extracting the plutonium by means of an immlscible solvent, such as dibutoxy dlethyletber.

Plutonium-241 processing: from impure oxide to high purity metal target disks

International Nuclear Information System (INIS)

Conner, W.V.; Baaso, D.L.

1975-01-01

The preparation of three plutonium-241 metal target disks, using a precision casting technique, is described. The disks were 0.625 inch in diameter and 0.125, 0.025, and 0.010 inch thick. All three disks were prepared simultaneously in a single casting. The variation in thickness of each disk was within +-1 percent of the disk's average thickness. The plutonium-241 was highly pure, and the finished disks contained a total of only 297 parts per million of detectable impurities. Purification of the plutonium oxide ( 241 PuO 2 ) and the conversion of the purified 241 PuO 2 to metal are also described. (U.S.)

Processing plutonium-contaminated soild for volume reduction using the segmented gate system

International Nuclear Information System (INIS)

Moroney, K.S.; Moroney, J.D.; Turney, J.M.; Doane, R.W.

1994-01-01

TMA/Eberline has developed and demonstrated an effective method for removing mixed plutonium and americium contamination from a coral soil matrix at the Defense Nuclear Agency's Johnston Atoll site. TMA's onsite soil processing for volume reduction is ongoing at a rate of over 2000 metric tons per week. The system uses arrays of sensitive radiation detectors coupled with sophisticated computer software developed by Eberline Instrument Corporation. The proprietary software controls four soil sorting units operating in parallel that utilize TMA's unique Segmented Gate System technology to remove radiologically contaminated soil from a moving supply on conveyor belts. Clean soil is released for use elsewhere on the island. Contaminated soil is diverted to either a metal drum for collecting higher activity open-quotes hotclose quotes particles (>5000 Becquerels), or to a supplementary soil washing process designed to remove finely divided particles of dispersed low level contamination. Site contamination limits specify maximum dispersed radioactivity of no more than 500 Becquerels per kilogram of soil averaged over no more than 0.1 cubic meter. Results of soil processing at this site have been excellent. After processing over 50,000 metric tons, the volume of contaminated material that would have required expensive special handling, packaging, and disposal as radioactive waste has been successfully reduced by over 98 percent. By mid-January 1994, nearly three million kiloBecquerels of plutonium/americium contamination had been physically separated from the contaminated feed by TMA's Segmented Gate System, and quality control sampling showed no radioactivity above release criteria in the open-quotes cleanclose quotes soil pile

Manual for the Epithermal Neutron Multiplicity Detector (ENMC) for Measurement of Impure MOX and Plutonium Samples

International Nuclear Information System (INIS)

Menlove, H. O.; Rael, C. D.; Kroncke, K. E.; DeAguero, K. J.

2004-01-01

We have designed a high-efficiency neutron detector for passive neutron coincidence and multiplicity counting of dirty scrap and bulk samples of plutonium. The counter will be used for the measurement of impure plutonium samples at the JNC MOX fabrication facility in Japan. The counter can also be used to create working standards from bulk process MOX. The detector uses advanced design "3He tubes to increase the efficiency and to shorten the neutron die-away time. The efficiency is 64% and the die-away time is 19.1 ?s. The Epithermal Neutron Multiplicity Counter (ENMC) is designed for high-precision measurements of bulk plutonium samples with diameters of less than 200 mm. The average neutron energy from the sample can be measured using the ratio of the inner ring of He-3 tubes to the outer ring. This report describes the hardware, performance, and calibration for the ENMC.

Appraisal of BWR plutonium burners for energy centers

International Nuclear Information System (INIS)

Williamson, H.E.

1976-01-01

The design of BWR cores with plutonium loadings beyond the self-generation recycle (SGR) level is investigated with regard to their possible role as plutonium burners in a nuclear energy center. Alternative plutonium burner approaches are also examined including the substitution of thorium for uranium as fertile material in the BWR and the use of a high-temperature gas reactor (HTGR) as a plutonium burner. Effects on core design, fuel cycle facility requirements, economics, and actinide residues are considered. Differences in net fissile material consumption among the various plutonium-burning systems examined were small in comparison to uncertainties in HTGR, thorium cycle, and high plutonium-loaded LWR technology. Variation in the actinide content of high-level wastes is not likely to be a significant factor in determining the feasibility of alternate systems of plutonium utilization. It was found that after 10,000 years the toxicity of actinide high-level wastes from the plutonium-burning fuel cycles was less than would have existed if the processed natural ores had not been used for nuclear fuel. The implications of plutonium burning and possible future fuel cycle options on uranium resource conservation are examined in the framework of current ERDA estimates of minable uranium resources

Chromium in aqueous nitrate plutonium process streams: Corrosion of 316 stainless steel and chromium speciation

International Nuclear Information System (INIS)

Smith, W.H.; Purdy, G.M.

1995-01-01

This study was undertaken to determine if chromium(+6) could exist in plutonium process solutions under normal operating conditions. Four individual reactions were studied: the rate of dissolution of stainless steel, which is the principal source of chromium in process solutions; the rate of oxidation of chromium(+3) to chromium(+6) by nitric acid; and the reduction of chromium(+6) back to chromium(+3) by reaction with stainless steel and with oxalic acid. The stainless steel corrosion rate was found to increase with increasing nitric acid concentration, increasing hydrofluoric acid concentration, and increasing temperature. Oxidation of chromium(+3) to chromium(+6) was negligible at room temperature and only became significant in hot concentrated nitric acid. The rate of reduction of chromium(+6) back to chromium(+3) by reaction with stainless steel or oxalic acid was found to be much greater than the rate of the reverse oxidation reaction. Based on these findings and taking into account normal operating conditions, it was determined that although there would be considerable chromium in plutonium process streams it would rarely be found in the (+6) oxidation state and would not exist in the (+6) state in the final process waste solutions

Chromium in aqueous nitrate plutonium process streams: Corrosion of 316 stainless steel and chromium speciation

International Nuclear Information System (INIS)

Smith, W.H.; Purdy, G.

1995-01-01

This study was undertaken to determine if chromium +6 could exist in plutonium process solutions under normal operating conditions. Four individual reactions were studied: the rate of dissolution of stainless steel, which is the principal source of chromium in process solutions; the rate of oxidation of chromium +3 to chromium +6 by nitric. acid; and the reduction of chromium +6 back to chromium +3 by reaction with stainless steel and with oxalic acid. The stainless steel corrosion rate was found to increase with increasing nitric acid concentration, increasing hydrofluoric acid concentration, and increasing temperature. Oxidation of chromium +3 to chromium +6 was negligible at room temperature and only became significant in hot concentrated nitric acid. The rate of reduction of chromium +6 back to chromium +3 by reaction with stainless steel or oxalic acid was found to be much greater than the rate of the reverse oxidation reaction. Based on these findings and taking into account normal operating conditions, it was determined that although there would be considerable chromium in plutonium process streams it would rarely be found in the +6 oxidation state and would not exist in the +6 state in the final process waste solutions

Civil plutonium management

International Nuclear Information System (INIS)

Sicard, B.; Zaetta, A.

2004-01-01

During 1960 and 1970 the researches on the plutonium recycling in fast neutrons reactors were stimulated by the fear of uranium reserves diminishing. At the beginning of 1980, the plutonium mono-recycling for water cooled reactors is implementing. After 1990 the public opinion concerning the radioactive wastes management and the consequences of the disarmament agreements between Russia and United States, modified the context. This paper presents the today situation and technology associated to the different options and strategical solutions of the plutonium management: the plutonium use in the world, the neutronic characteristics, the plutonium effect on the reactors characteristics, the MOX behavior in the reactors, the MOX fabrication and treatment, the possible improvements to the plutonium use, the concepts performance in a nuclear park. (A.L.B.)

Acid-digestion treatment of plutonium-containing waste

International Nuclear Information System (INIS)

Wieczorek, H.; Kemmler, G.; Krause, H.

1981-01-01

The Radioactive Acid-Digestion Test Unit (RADTU) has been constructed at Hanford to demonstrate the application of the acid-digestion process for treating combustible transuranic wastes and scrap materials. The RADTU, with its original tray digestion vessel, has recently completed a six-month campaign processing potentially contaminated non-glovebox wastes from a Hanford plutonium facility. During this campaign, it processed 2100 kg largely cellulosic wastes at an average sustained processing rate of 3 kg/h as limited by the acid-waste contact and the water boil-off rate from the acid feeds. The on-line operating efficiency was nearly 50% on a twelve-hour day, five-day week basis. Following this campaign, a new annular high-rate digester has been installed for testing. In preliminary tests with simulated wastes, the new digester demonstrated a sustained capacity of 10 kg/h with greatly improved intimacy of contact between the digestion acid and the waste. The new design also doubles the heat-transfer surface, which is expected to provide at least twice the water boil-off rate of the previous tray digester design. Following shakedown testing with simulated and low-level wastes, the new unit will be used to process combustible plutonium scrap and waste from Hanford plutonium facilities for the purposes of volume reduction, plutonium recovery, and stabilization of the final waste form. (author)

Uranium and plutonium distribution in unirradiated mixed oxide fuel from industrial fabrication

International Nuclear Information System (INIS)

Hanus, D.; Kleykamp, H.

1982-01-01

Different process variants developed in the last few years by the firm ALKEM to manufacture FBR and LWR mixed oxide fuel are given. The uranium and plutonium distribution is determined on the pellets manufactured with the help of the electron beam microprobe. The stepwise improvement of the uranium-plutonium homogeneity in the short-term developed granulate variants and in the long-term developed new processes are illustrated starting with early standard processes for FBR fuel. An almost uniform uranium-plutonium distribution could be achieved for the long-term developed new processes (OKOM, AuPuC). The uranium-plutonium homogeneity are quantified in the pellets manufactured according to the considered process variants with a newly defined quality number. (orig.)

Contribution to the study of the process of purification of plutonium by extraction with trilaurylamine

International Nuclear Information System (INIS)

Saey, Jean-Claude

1966-01-01

This work addresses the process of plutonium purification which uses trilaurylamine nitrate. In order to use this nitrate in its solid state and at ordinary temperature, a secondary solvent must be added which must have some properties: low volume mass and viscosity, high boiling and ignition temperatures, rather low miscibility with water, high stability in front of joint actions of nitric acid and radiations, and no reaction with the alkylammonium nitrate and the complex. Thus, the author addresses phenomena of immiscibility and identifies some important molecular characteristics which could lead to the selection of another secondary solvent than dodecane. The decalin seem interesting and its behaviour is studied. A mixing of dodecane and decalin is used as extraction mixing. The obtained results are discussed. Finally, the author notices that using this mixing in the plutonium purification process results in a large increase of metal concentrations and a decrease of risks of crystallisation, without any major drawback, in a continuously operating micro-industrial installation

Design of an integrated non-destructive plutonium assay facility

International Nuclear Information System (INIS)

Moore, C.B.

1984-01-01

The Department of Energy requires improved technology for nuclear materials accounting as an essential part of new plutonium processing facilities. New facilities are being constructed at the Savannah River Plant by the Du Pont Company, Operating Contractor, to recover plutonium from scrap and waste material generated at SRP and other DOE contract processing facilities. This paper covers design concepts and planning required to incorporate state-of-the-art plutonium assay instruments developed at several national laboratories into an integrated, at-line nuclear material accounting facility operating in the production area. 3 figures

Photochemical technique for reduction of uranium and subsequently plutonium in the Purex process

International Nuclear Information System (INIS)

Goldstein, M.; Barker, J.J.; Gangwer, T.

1976-09-01

A photochemical modification of the Purex process is described in which a purified side stream of UO 2 ++ ion is reduced to U +4 outside the radioactive area of the reprocessing plant. The U +4 is then cycled back to step 2 of the Purex process to reduce the plutonium and effect separation within the partitioning column. This process is shown to be very energy efficient and compatible with existing conventional lamp technology. Preliminary cost estimates of the energy requirements for photon production are essentially negligible. Conceptual systems and photochemical reactor designs are presented. Potential benefits of this system are discussed

Natural hazards that may trigger a radiological release from a plutonium processing facility

Energy Technology Data Exchange (ETDEWEB)

Selvidge, J. E.

1977-04-28

Calculations show the probability of a tornado striking a plutonium area at Rocky Flats is 2.2 x 10/sup -4/ per year. The source term (expected value of plutonium release) should such an event occur is calculated at 3.3 x 10/sup -7/ grams. The source term for high-velocity, downslope winds is higher--2.2 x 10/sup -3/ grams. The probability of a meteorite that weighs one or more pounds (453 grams) striking a plutonium area is estimated at 8.88 x 10/sup -7/ per year. Because of this small probability and the remote chance that a plutonium release would occur even if a meteorite hit occurred, the hazard from meteorite impact is considered negligible. Conservative assumptions result in all calculated frequencies being almost certainly too high. Empirical observations have indicated lower frequencies than those calculated.

Natural hazards that may trigger a radiological release from a plutonium processing facility

International Nuclear Information System (INIS)

Selvidge, J.E.

1977-01-01

Calculations show the probability of a tornado striking a plutonium area at Rocky Flats is 2.2 x 10 -4 per year. The source term (expected value of plutonium release) should such an event occur is calculated at 3.3 x 10 -7 grams. The source term for high-velocity, downslope winds is higher--2.2 x 10 -3 grams. The probability of a meteorite that weighs one or more pounds (453 grams) striking a plutonium area is estimated at 8.88 x 10 -7 per year. Because of this small probability and the remote chance that a plutonium release would occur even if a meteorite hit occurred, the hazard from meteorite impact is considered negligible. Conservative assumptions result in all calculated frequencies being almost certainly too high. Empirical observations have indicated lower frequencies than those calculated

Characteristics of airborne plutonium resuspended from near-background aged surface-sources

International Nuclear Information System (INIS)

Sehmel, G.A.

1982-11-01

Plutonium content in samples of airborne solids collected at five Hanford sites was determined in several experiments directed toward investigating resuspension processes for aged surface sources. Though airborne plutonium concentrations are extremely low, radiochemical technique sensitivities allow plutonium characterization to be considered as a function of host-particle diameter in samples of airborne solids. Plutonium concentrations and activity densities are a function of aerodynamic particle diameter, sampling height, wind speed, wind direction and plutonium isotopic ratios

Chemical species of plutonium in Hanford radioactive tank waste

International Nuclear Information System (INIS)

Barney, G.S.

1997-01-01

Large quantities of radioactive wastes have been generated at the Hanford Site over its operating life. The wastes with the highest activities are stored underground in 177 large (mostly one million gallon volume) concrete tanks with steel liners. The wastes contain processing chemicals, cladding chemicals, fission products, and actinides that were neutralized to a basic pH before addition to the tanks to prevent corrosion of the steel liners. Because the mission of the Hanford Site was to provide plutonium for defense purposes, the amount of plutonium lost to the wastes was relatively small. The best estimate of the amount of plutonium lost to all the waste tanks is about 500 kg. Given uncertainties in the measurements, some estimates are as high as 1,000 kg (Roetman et al. 1994). The wastes generally consist of (1) a sludge layer generated by precipitation of dissolved metals from aqueous wastes solutions during neutralization with sodium hydroxide, (2) a salt cake layer formed by crystallization of salts after evaporation of the supernate solution, and (3) an aqueous supernate solution that exists as a separate layer or as liquid contained in cavities between sludge or salt cake particles. The identity of chemical species of plutonium in these wastes will allow a better understanding of the behavior of the plutonium during storage in tanks, retrieval of the wastes, and processing of the wastes. Plutonium chemistry in the wastes is important to criticality and environmental concerns, and in processing the wastes for final disposal. Plutonium has been found to exist mainly in the sludge layers of the tanks along with other precipitated metal hydrous oxides. This is expected due to its low solubility in basic aqueous solutions. Tank supernate solutions do not contain high concentrations of plutonium even though some tanks contain high concentrations of complexing agents. The solutions also contain significant concentrations of hydroxide which competes with other

History and stabilization of the Plutonium Finishing Plant (PFP) complex, Hanford Site

Energy Technology Data Exchange (ETDEWEB)

Gerber, M.S., Fluor Daniel Hanford

1997-02-18

The 231-Z Isolation Building or Plutonium Metallurgy Building is located in the Hanford Site`s 200 West Area, approximately 300 yards north of the Plutonium Finishing Plant (PFP) (234-5 Building). When the Hanford Engineer Works (HEW) built it in 1944 to contain the final step for processing plutonium, it was called the Isolation Building. At that time, HEW used a bismuth phosphate radiochemical separations process to make `AT solution,` which was then dried and shipped to Los Alamos, New Mexico. (AT solution is a code name used during World War II for the final HEW product.) The process was carried out first in T Plant and the 224-T Bulk Reduction Building and B Plant and the 224-B Bulk Reduction Building. The 224-T and -B processes produced a concentrated plutonium nitrate stream, which then was sent in 8-gallon batches to the 231-Z Building for final purification. In the 231-Z Building, the plutonium nitrate solution underwent peroxide `strikes` (additions of hydrogen peroxide to further separate the plutonium from its carrier solutions), to form the AT solution. The AT solution was dried and shipped to the Los Alamos Site, where it was made into metallic plutonium and then into weapons hemispheres.` The 231-Z Building began `hot` operations (operations using radioactive materials) with regular runs of plutonium nitrate on January 16, 1945.

A portable concentrator for processing plutonium

International Nuclear Information System (INIS)

Chamberlain, D.B.; Conner, C.; Chen, L.

1995-01-01

A horizontal, agitated film concentrator designed to concentrate liquid streams to a high solid content slurry is briefly described. The Rototherm unit is being studied for use at US Department of Energy facilities to handle large quantities of aqueous plutonium solutions. Capabilities for evaporating more than 98% of the water present in a single pass have been demonstrated. Decontamination factors of 10 6 to 10 7 are expected. The unit may also be useful for recycling aqueous waste treatment reagents from the decontamination of gaseous diffusion plants

The plutonium society

International Nuclear Information System (INIS)

Mez, L.; Richter, M.

1981-01-01

The lectures of an institute are reported on, which took place between 25th and 27th January 1980 in Berlin. The subsequent public panel discussion with representations from the political parties is then documentated in a few press-reports. The themes of the 8 lectures are: views and facts on plutonium, plutonium as an energy resource, military aspects of the production of plutonium, economic aspects of the plutonium economy, the position of the trade unions on the industrial reconversion, the alleged inevitability of a plutonium society and the socio-political alternatives and perspectives of nuclear waste disposal. (UA) [de

Purification process of uranium hexafluoride containing traces of plutonium fluoride and/or neptunium fluoride

International Nuclear Information System (INIS)

Aubert, J.; Bethuel, L.; Carles, M.

1983-01-01

In this process impure uranium hexafluoride is contacted with a metallic fluoride chosen in the group containing lead fluoride PbF 2 , uranium fluorides UFsub(4+x) (0 3 at a temperature such as plutonium and/or neptunium are reduced and pure uranium hexafluoride is recovered. Application is made to uranium hexafluoride purification in spent fuel reprocessing [fr

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

Energy Technology Data Exchange (ETDEWEB)

1993-05-15

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

What is plutonium stabilization, and what is safe storage of plutonium?

International Nuclear Information System (INIS)

Forsberg, C.W.

1995-01-01

The end of the cold war has resulted in the shutdown of nuclear weapons production and the start of dismantlement of significant numbers of nuclear weapons. This, in turn, is creating an inventory of plutonium requiring interim and long-term storage. A key question is, ''What is required for safe, multidecade, plutonium storage?'' The requirements for storage, in turn, define what is needed to stabilize the plutonium from its current condition into a form acceptable for interim and long-term storage. Storage requirements determine if research is required to (1) define required technical conditions for interim and long-term storage and (2) develop or improve current stabilization technologies. Storage requirements depend upon technical, policy, and economic factors. The technical issues are complicated by several factors. Plutonium in aerosol form is highly hazardous. Plutonium in water is hazardous. The plutonium inventory is in multiple chemical forms--some of which are chemically reactive. Also, some of the existing storage forms are clearly unsuitable for storage periods over a few years. Gas generation by plutonium compounds complicates storage: (1) all plutonium slowly decays creating gaseous helium and (2) the radiation from plutonium decay can initiate many chemical reactions-some of which generate significant quantities of gases. Gas generation can pressurize sealed storage packages. Last nuclear criticality must be avoided

Imperatives for using plutonium in commercial power reactors

International Nuclear Information System (INIS)

Sandquist, G.M.; Kunze, J.F.

1995-01-01

The use of reprocessed or newly produced plutonium as a fissile fuel in commercial nuclear reactors in the US has been actively suppressed by the current US Administration. Yet, many other advanced nations have already adopted mixed oxide fuels which are manufactured from a mixture of plutonium and natural uranium compounds. These nations have successfully proven the use of such nuclear fuel in their commercial power reactors for many years. The full consequence of the restrictive nuclear policy in the US will greatly limit the lifetime of the nuclear fuel resources in the US from a nominal potential of 100 centuries or more of potential energy supply to about 50 years or less at economical prices for uranium. This paper addresses both the imperatives and the potential and the perceived hazards of plutonium utilization and examines the consequences of government policy regarding utilization of nuclear power

EDF research scenarios for closing the Plutonium cycle

International Nuclear Information System (INIS)

Le Mer, Joël; Garzenne, Claude; Lemasson, David

2013-01-01

Conclusion: → There are various solutions to plutonium fuel closure; → Natural uranium consumption is reduced: • Full generation IV fleet is obviously the most efficient; • Symbiotic fleet makes a better use of its advanced reactors. → Plutonium inventory reaches an equilibrium between 700 tons and 1150 tons. • The multi-recycling of spent MOX fuel must be a long term solution in order to reduce significantly the plutonium inventory. → Spent fuel storage is reduced when MOX spent fuel are reprocessed but sodium pools are challenging. → Fast reactors are not the only solution to use MOX spent fuel: • HCPWR is a roundabout solution: – the reduction of natural uranium is limited; – the high level waste production is high. – The reprocessing plant capacity must be increased during deployment phase → R&D must be continued to improve HCPWR design

Status of plutonium ceramic immobilization processes and immobilization forms

International Nuclear Information System (INIS)

Ebbinghaus, B.B.; Van Konynenburg, R.A.; Vance, E.R.; Jostsons, A.

1996-01-01

Immobilization in a ceramic followed by permanent emplacement in a repository or borehole is one of the alternatives currently being considered by the Fissile Materials Disposition Program for the ultimate disposal of excess weapons-grade plutonium. To make Pu recovery more difficult, radioactive cesium may also be incorporated into the immobilization form. Valuable data are already available for ceramics form R ampersand D efforts to immobilize high-level and mixed wastes. Ceramics have a high capacity for actinides, cesium, and some neutron absorbers. A unique characteristic of ceramics is the existence of mineral analogues found in nature that have demonstrated actinide immobilization over geologic time periods. The ceramic form currently being considered for plutonium disposition is a synthetic rock (SYNROC) material composed primarily of zirconolite (CaZrTi 2 O 7 ), the desired actinide host phase, with lesser amounts of hollandite (BaAl 2 Ti 6 O 16 ) and rutile (TiO 2 ). Alternative actinide host phases are also being considered. These include pyrochlore (Gd 2 Ti 2 O 7 ), zircon (ZrSiO 4 ), and monazite (CePO 4 ), to name a few of the most promising. R ampersand D activities to address important technical issues are discussed. Primarily these include moderate scale hot press fabrications with plutonium, direct loading of PuO 2 powder, cold press and sinter fabrication methods, and immobilization form formulation issues

Water Solubility of Plutonium and Uranium Compounds and Residues at TA-55

International Nuclear Information System (INIS)

Reilly, Sean Douglas; Smith, Paul Herrick; Jarvinen, Gordon D.; Prochnow, David Adrian; Schulte, Louis D.; DeBurgomaster, Paul Christopher; Fife, Keith William; Rubin, Jim; Worl, Laura Ann

2016-01-01

Understanding the water solubility of plutonium and uranium compounds and residues at TA-55 is necessary to provide a technical basis for appropriate criticality safety, safety basis and accountability controls. Individual compound solubility was determined using published solubility data and solution thermodynamic modeling. Residue solubility was estimated using a combination of published technical reports and process knowledge of constituent compounds. The scope of materials considered includes all compounds and residues at TA-55 as of March 2016 that contain Pu-239 or U-235 where any single item in the facility has more than 500 g of nuclear material. This analysis indicates that the following materials are not appreciably soluble in water: plutonium dioxide (IDC=C21), plutonium phosphate (IDC=C66), plutonium tetrafluoride (IDC=C80), plutonium filter residue (IDC=R26), plutonium hydroxide precipitate (IDC=R41), plutonium DOR salt (IDC=R42), plutonium incinerator ash (IDC=R47), uranium carbide (IDC=C13), uranium dioxide (IDC=C21), U 3 O 8 (IDC=C88), and uranium filter residue (IDC=R26). This analysis also indicates that the following materials are soluble in water: plutonium chloride (IDC=C19) and uranium nitrate (IDC=C52). Equilibrium calculations suggest that PuOCl is water soluble under certain conditions, but some plutonium processing reports indicate that it is insoluble when present in electrorefining residues (R65). Plutonium molten salt extraction residues (IDC=R83) contain significant quantities of PuCl 3 , and are expected to be soluble in water. The solubility of the following plutonium residues is indeterminate due to conflicting reports, insufficient process knowledge or process-dependent composition: calcium salt (IDC=R09), electrorefining salt (IDC=R65), salt (IDC=R71), silica (IDC=R73) and sweepings/screenings (IDC=R78). Solution thermodynamic modeling also indicates that fire suppression water buffered with a commercially-available phosphate

Water Solubility of Plutonium and Uranium Compounds and Residues at TA-55

Energy Technology Data Exchange (ETDEWEB)

Reilly, Sean Douglas [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Smith, Paul Herrick [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Jarvinen, Gordon D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Prochnow, David Adrian [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Schulte, Louis D. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; DeBurgomaster, Paul Christopher [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Fife, Keith William [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Rubin, Jim [Los Alamos National Lab. (LANL), Los Alamos, NM (United States; Worl, Laura Ann [Los Alamos National Lab. (LANL), Los Alamos, NM (United States

2016-06-13

Understanding the water solubility of plutonium and uranium compounds and residues at TA-55 is necessary to provide a technical basis for appropriate criticality safety, safety basis and accountability controls. Individual compound solubility was determined using published solubility data and solution thermodynamic modeling. Residue solubility was estimated using a combination of published technical reports and process knowledge of constituent compounds. The scope of materials considered includes all compounds and residues at TA-55 as of March 2016 that contain Pu-239 or U-235 where any single item in the facility has more than 500 g of nuclear material. This analysis indicates that the following materials are not appreciably soluble in water: plutonium dioxide (IDC=C21), plutonium phosphate (IDC=C66), plutonium tetrafluoride (IDC=C80), plutonium filter residue (IDC=R26), plutonium hydroxide precipitate (IDC=R41), plutonium DOR salt (IDC=R42), plutonium incinerator ash (IDC=R47), uranium carbide (IDC=C13), uranium dioxide (IDC=C21), U₃O₈ (IDC=C88), and uranium filter residue (IDC=R26). This analysis also indicates that the following materials are soluble in water: plutonium chloride (IDC=C19) and uranium nitrate (IDC=C52). Equilibrium calculations suggest that PuOCl is water soluble under certain conditions, but some plutonium processing reports indicate that it is insoluble when present in electrorefining residues (R65). Plutonium molten salt extraction residues (IDC=R83) contain significant quantities of PuCl₃, and are expected to be soluble in water. The solubility of the following plutonium residues is indeterminate due to conflicting reports, insufficient process knowledge or process-dependent composition: calcium salt (IDC=R09), electrorefining salt (IDC=R65), salt (IDC=R71), silica (IDC=R73) and sweepings/screenings (IDC=R78). Solution thermodynamic modeling also indicates that fire suppression water buffered with a

Solubility of Plutonium (IV) Oxalate During Americium/Curium Pretreatment

International Nuclear Information System (INIS)

Rudisill, T.S.

1999-01-01

Approximately 15,000 L of solution containing isotopes of americium and curium (Am/Cm) will undergo stabilization by vitrification at the Savannah River Site (SRS). Prior to vitrification, an in-tank pretreatment will be used to remove metal impurities from the solution using an oxalate precipitation process. Material balance calculations for this process, based on solubility data in pure nitric acid, predict approximately 80 percent of the plutonium in the solution will be lost to waste. Due to the uncertainty associated with the plutonium losses during processing, solubility experiments were performed to measure the recovery of plutonium during pretreatment and a subsequent precipitation process to prepare a slurry feed for a batch melter. A good estimate of the plutonium content of the glass is required for planning the shipment of the vitrified Am/Cm product to Oak Ridge National Laboratory (ORNL).The plutonium solubility in the oxalate precipitation supernate during pretreatment was 10 mg/mL at 35 degrees C. In two subsequent washes with a 0.25M oxalic acid/0.5M nitric acid solution, the solubility dropped to less than 5 mg/mL. During the precipitation and washing steps, lanthanide fission products in the solution were mostly insoluble. Uranium, and alkali, alkaline earth, and transition metal impurities were soluble as expected. An elemental material balance for plutonium showed that greater than 94 percent of the plutonium was recovered in the dissolved precipitate. The recovery of the lanthanide elements was generally 94 percent or higher except for the more soluble lanthanum. The recovery of soluble metal impurities from the precipitate slurry ranged from 15 to 22 percent. Theoretically, 16 percent of the soluble oxalates should have been present in the dissolved slurry based on the dilution effects and volumes of supernate and wash solutions removed. A trace level material balance showed greater than 97 percent recovery of americium-241 (from the beta dec

Simulation and control synthesis for a pulse column separation system for plutonium--uranium recovery

International Nuclear Information System (INIS)

McCutcheon, E.B.

1975-05-01

Control of a plutonium-uranium partitioning column was studied using a mathematical model developed to simulate the dynamic response and to test postulated separation mechanisms. The column is part of a plutonium recycle flowsheet developed for the recovery of plutonium and uranium from metallurgical scrap. In the first step of the process, decontamination from impurities is achieved by coextracting plutonium and uranium in their higher oxidation states. In the second step, reduction of the plutonium to a lower oxidation state allows partitioning of the plutonium and uranium. The use of hydroxylamine for the plutonium reduction in this partitioning column is a unique feature of the process. The extraction operations are carried out in pulse columns. (U.S.)

Plutonium immobilization plant using ceramic in existing facilities at the Savannah River site

International Nuclear Information System (INIS)

DiSabatino, A.

1998-01-01

The Plutonium Immobilization Plant (PIP) accepts plutonium (Pu) from pit conversion and from non-pit sources, and through a ceramic immobilization process converts the plutonium into an immobilized form that can be disposed of in a high level waste (HLW) repository. This immobilization process is shown conceptually in Figure 1-1. The objective is to make an immobilized form, suitable for geologic disposal, in which the plutonium is as inherently unattractive and inaccessible as the plutonium in spent fuel from commercial reactors. The ceramic immobilization alternative presented in this report consists of first converting the surplus material to an oxide, followed by incorporating the plutonium oxide into a titanate-based ceramic material that is placed in metal cans

Plutonium solubilities

International Nuclear Information System (INIS)

Puigdomnech, I.; Bruno, J.

1991-02-01

Thermochemical data has been selected for plutonium oxide, hydroxide, carbonate and phosphate equilibria. Equilibrium constants have been evaluated in the temperature range 0 to 300 degrees C at a pressure of 1 bar to T≤100 degrees C and at the steam saturated pressure at higher temperatures. Measured solubilities of plutonium that are reported in the literature for laboratory experiments have been collected. Solubility data on oxides, hydroxides, carbonates and phosphates have been selected. No solubility data were found at temperatures higher than 60 degrees C. The literature solubility data have been compared with plutonium solubilities calculated with the EQ3/6 geochemical modelling programs, using the selected thermodynamic data for plutonium. (authors)

Idaho Chemical Processing Plant and Plutonium-Uranium Extraction Plant phaseout/deactivation study

International Nuclear Information System (INIS)

Patterson, M.W.; Thompson, R.J.

1994-01-01

The decision to cease all US Department of Energy (DOE) reprocessing of nuclear fuels was made on April 28, 1992. This study provides insight into and a comparison of the management, technical, compliance, and safety strategies for deactivating the Idaho Chemical Processing Plant (ICPP) at Westinghouse Idaho Nuclear Company (WINCO) and the Westinghouse Hanford Company (WHC) Plutonium-Uranium Extraction (PUREX) Plant. The purpose of this study is to ensure that lessons-learned and future plans are coordinated between the two facilities

Plutonium in uranium deposits

International Nuclear Information System (INIS)

Curtis, D.; Fabryka-Martin, J.; Aguilar, R.; Attrep, M. Jr.; Roensch, F.

1992-01-01

Plutonium-239 (t 1/2 , 24,100 yr) is one of the most persistent radioactive constituents of high-level wastes from nuclear fission power reactors. Effective containment of such a long-lived constituent will rely heavily upon its containment by the geologic environment of a repository. Uranium ore deposits offer a means to evaluate the geochemical properties of plutonium under natural conditions. In this paper, analyses of natural plutonium in several ores are compared to calculated plutonium production rates in order to evaluate the degree of retention of plutonium by the ore. The authors find that current methods for estimating production rates are neither sufficiently accurate nor precise to provide unambiguous measures of plutonium retention. However, alternative methods for evaluating plutonium mobility are being investigated, including its measurement in natural ground waters. Preliminary results are reported and establish the foundation for a comprehensive characterization of plutonium geochemistry in other natural environments

The US plutonium materials conversion program in Russia

International Nuclear Information System (INIS)

Zygmunt, S.J.; Mason, C.F.V.; Hahn, W.K.

2000-01-01

Progress has been made in Russia towards the conversion of weapons-grade plutonium (w-Pu) into plutonium oxide (PuO 2 ) suitable for further manufacture into mixed oxide (MOX) fuels. This program was started in 1998 in response to US proliferation concerns and the acknowledged international need to decrease the available weapons-grade Pu. A similar agenda is being followed in the US to address disposition of US surplus weapons-grade Pu. In Russia a conversion process has been selected and a site proposed. This paper discusses the present state of the program in support of this future operating facility that will process up to 5 metric tons of plutonium a year. (authors)

The use of plutonium

International Nuclear Information System (INIS)

Marshall, W.

1980-01-01

The use of plutonium as a vital energy source producing maximum economic benefit with minimum proliferation risks is discussed. Having considered the production of plutonium, several possible plutonium fuel cycle options are identified and the economic value to be attached to plutonium for each examined. It is shown how the use of plutonium in fast reactors gives an opportunity for a non-proliferation policy not available when plutonium is used only in thermal reactors. From the technical considerations reviewed concerning plutonium and fast reactors it is shown that an economic regime involving international trade in spent thermal reactor fuel is possible which benefits equally those countries with fast reactors and those without and also assists in avoiding the proliferation of nuclear weapons. (U.K.)

Plutonium-238 and plutonium-239 metabolism in dairy cows following ingestion of mixed oxides

International Nuclear Information System (INIS)

Patzer, R.G.; Mullen, A.A.; Sutton, W.W.; Potter, G.D.; Mosley, R.E.; Efurd, D.W.; Stalnaker, N.D.

1985-01-01

Dairy cows were given oral dosage of plutonium-238 and plutonium-239 dioxide particles in a study to determine the relative gastrointestinal absorption and tissue distribution of the nuclides. Two cows were given particles in which the two isotopes were homogeneously mixed within the particles. A third cow was given two batches of particles which contained either plutonium-238 or plutonium-239. Results indicate that, when the two isotopes of plutonium are homogeneous within the particles, there is no difference between plutonium-238 and plutonium-239 in the relative gastrointestinal absorption and tissue distribution

High-temperature enthalpies of plutonium monocarbide and plutonium sesquicarbide

International Nuclear Information System (INIS)

Oetting, F.L.

1979-01-01

The high-temperature enthalpies of plutonium monocarbide and plutonium sesquicarbide have been determined with a copper-block calorimeter of the isoperibol type. The experimental enthalpy data, which was measured relative to 298 K, covered the temperature range from 400 to 1500 K. The calculation of the temperature rise of the calorimeter takes into account the added heat evolution from the radioactive decay of the plutonium samples. These enthalpy results, combined with the heat capacity and entropy of the respective carbide at 298 K available from the literature, has made it possible to generate tables of thermodynamic functions for the plutonium carbides. The behavior of the heat capacity of both of the plutonium carbides, i.e., a relatively steep increase in the heat capacity as the temperature increases, may be attributed to a premelting effect with the formation of vacancies within the crystal lattice although a theoretical treatment of this phenomenon is not given

Inert atmosphere system for plutonium processing gloveboxes

International Nuclear Information System (INIS)

Bogard, C.F.; Calkins, K.W.; Rogers, R.F.

1975-01-01

Recent efforts to reduce fire hazards in plutonium processing operations are described. In such operations, the major environmental controls are developed through various kinds of glovebox systems. In evaluating the air-atmosphere glovebox systems, formerly in use at Rocky Flats and many other plants, a decision was made to convert to a recirculating ''inert'' atmosphere. The inert atmosphere consists of nitrogen, supplied from an on-site generating plant, diluting oxygen content to one to 5 percent by volume. Problems encountered during the change over included: determination of all factors influencing air leakage into the system, and reducing leakage to the practical minimum; meeting all fire and safety standards on the filter plenum and exhaust systems; provision for converting portions of the system to an air atmosphere to conduct maintenance work; inclusion of oxygen analyzers throughout the system to check gas quality and monitor for leaks; and the use of automatic controls to protect against a variety of potential malfunctions. The current objectives to reduce fire hazards have been met and additional safeguards were added. The systems are operating satisfactorily. (U.S.)

Study of plutonium cycle in marine ecosystems

International Nuclear Information System (INIS)

Merino Pareja, J.; Sanchez Cabeza, J. A.; Molero Savall, J.; Masque Barri, P.

1998-01-01

The distribution, transport and accumulation mechanisms of transuranics (and other radionuclides) in the marine environment depend on the source term, biogeochemical cycles, transport with the water masses, sedimentation processes and transfer mechanisms in the trophic chain. The biogeochemical behaviour of plutonium, which has been the focus of our work, was studied using the following approaches: determination of the physico-chemical speciation of plutonium in marine waters, vertical flux in the water column, uptake by marine organisms (phytoplankton and zooplankton) and distribution in dements cores. A preliminary model of the accumulation and distribution of plutonium in the first levels of the marine food chain in the Irish Sea has also been formulated. All this information allowed us to obtain an integrated view of the behaviour of plutonium in the marine environment. (Author) 14 refs

Extraction of plutonium from lean residues by room-temperature fluoride volatility

International Nuclear Information System (INIS)

Campbell, G.M.; Foropoulos, J.; Kennedy, R.C.; Dye, B.A.; Behrens, R.G.

1990-01-01

The use of dioxygen difluoride and krypton difluoride for the recovery of plutonium from lean residues by conversion to gaseous plutonium hexa-fluoride is being investigated. The synthesis of dioxygen difluoride in practical quantity has been demonstrated. Fluorination of plutonium compounds under ideal conditions supports the contention that a viable process can be developed. Application of the method to lean plutonium residues is in the early stage of development

AN ADVANCED OXIDATION PROCESS : FENTON PROCESS

Directory of Open Access Journals (Sweden)

Engin GÜRTEKİN

2008-03-01

Full Text Available Biological wastewater treatment is not effective treatment method if raw wastewater contains toxic and refractory organics. Advanced oxidation processes are applied before or after biological treatment for the detoxification and reclamation of this kind of wastewaters. The advanced oxidation processes are based on the formation of powerful hydroxyl radicals. Among advanced oxidation processes Fenton process is one of the most promising methods. Because application of Fenton process is simple and cost effective and also reaction occurs in a short time period. Fenton process is applied for many different proposes. In this study, Fenton process was evaluated as an advanced oxidation process in wastewater treatment.

Extrinsic and intrinsic complexities of the Los Alamos plutonium processing facility

International Nuclear Information System (INIS)

Bearse, R.C.; Roberts, N.J.; Longmire, V.L.

1985-01-01

Analysis of the data obtained in one year of plutonium accounting at Los Alamos reveals significant complexity. Much of this complexity arises from the complexity of the processes themselves. Additional complexity is induced by errors in the data entry process. It is important to note that there is no evidence that this complexity is adversely affecting the accounting in the plant. The authors have been analyzing transaction data from fiscal year 1983 processing. This study involved 62,595 transactions. The data have been analyzed using the relational database program INGRES on a VAX 11/780 computer. This software allows easy manipulation of the original data and subsets drawn from it. The authors have been attempting for several years to understand the global features of the TA-55 accounting data. This project has underscored several of the system's complexities

Study of the potential use of carburized niobium in plutonium processing

International Nuclear Information System (INIS)

Johnson, M.J.

1998-01-01

Carburized refractory metals, especially tantalum, have been shown to possess properties useful for application as hardware in the plutonium-processing environment. These applications are driven in part by a desire to minimize the production of radioactively contaminated waste. The current use of ceramics as containment materials for Pu processing are not ideal due to the short service life of the hardware, placing an additional burden on the contaminated waste stream. Carburized niobium has been examined for use as an improved hardware material. The Nb-C system is analogous to the previously studied Ta-C system. The low density of niobium relative to tantalum will improve the ergonomics of the glovebox environment. The choice of the Nb-C system will be supported by a thermodynamic and kinetic analysis. Preliminary results of the processing investigation also will be presented

Plutonium

International Nuclear Information System (INIS)

Koelzer, W.

1989-03-01

This report contains with regard to 'plutonium' statements on chemistry, occurrence and reactions in the environment, handling procedures in the nuclear fuel cycle, radiation protection methods, biokinetics, toxicology and medical treatment to make available reliable data for the public discussion on plutonium especially its use in nuclear power plants and its radiological assessment. (orig.) [de

Plutonium

International Nuclear Information System (INIS)

Mueller-Christiansen, K.; Wollesen, M.

1979-01-01

As emotions and fear of plutonium are neither useful for the non-professionals nor for the political decision makers and the advantages and disadvantages of plutonium can only put against each other under difficulties, the paper wants to present the most essential scientific data of plutonium in a generally understandable way. Each of the individual sections is concluded and they try to give an answer to the most discussed questions. In order to make understanding easier, the scientific facts are only brought at points where it cannot be done without for the correctness of the presentation. Many details were left out knowingly. On the other hand, important details are dealt with several times if it seems necessary for making the presentation correct. The graphical presentations and the figures in many cases contain more than said in the text. They give the interested reader hints to scientific-technical coherences. The total material is to enable the reader to form his own opinion on plutonium problems which are being discussed in public. (orig./HP) [de

Status of plutonium ceramic immobilization processes and immobilization forms

Energy Technology Data Exchange (ETDEWEB)

Ebbinghaus, B.B.; Van Konynenburg, R.A. [Lawrence Livermore National Lab., CA (United States); Vance, E.R.; Jostsons, A. [Australian Nuclear Science and Technology Organization, Menai (Australia)] [and others

1996-05-01

Immobilization in a ceramic followed by permanent emplacement in a repository or borehole is one of the alternatives currently being considered by the Fissile Materials Disposition Program for the ultimate disposal of excess weapons-grade plutonium. To make Pu recovery more difficult, radioactive cesium may also be incorporated into the immobilization form. Valuable data are already available for ceramics form R&D efforts to immobilize high-level and mixed wastes. Ceramics have a high capacity for actinides, cesium, and some neutron absorbers. A unique characteristic of ceramics is the existence of mineral analogues found in nature that have demonstrated actinide immobilization over geologic time periods. The ceramic form currently being considered for plutonium disposition is a synthetic rock (SYNROC) material composed primarily of zirconolite (CaZrTi{sub 2}O{sub 7}), the desired actinide host phase, with lesser amounts of hollandite (BaAl{sub 2}Ti{sub 6}O{sub 16}) and rutile (TiO{sub 2}). Alternative actinide host phases are also being considered. These include pyrochlore (Gd{sub 2}Ti{sub 2}O{sub 7}), zircon (ZrSiO{sub 4}), and monazite (CePO{sub 4}), to name a few of the most promising. R&D activities to address important technical issues are discussed. Primarily these include moderate scale hot press fabrications with plutonium, direct loading of PuO{sub 2} powder, cold press and sinter fabrication methods, and immobilization form formulation issues.

On-line monitoring of low-level plutonium concentrations

International Nuclear Information System (INIS)

Hofstetter, K.J.; Huff, G.A.; Rebagay, T.V.

1979-10-01

An on-line monitor has been developed to assay plutonium in nitric acid solutions. The performance of the monitor has been assessed by a laboratory experimentation program using solutions with plutonium concentrations from 0.1 to 10 g/l. These conditions are typical of the plutonium solutions in an input stream to a plutonium-purification cycle in a reprocessing plant following uranium/plutonium partitioning. The monitoring system can be fully automated and shows great promise for detecting and quantifying plutonium in situ, thus minimizing the reliance on traditional sampling and laboratory-analysis techniques. The total concentration and isotopic abundance of plutonium are determined by measuring the absolute intensities of the low-energy gamma rays characteristics of 238 Pu, 239 Pu, and 240 Pu nuclides by direct gamma-ray spectroscopy and computer analysis of the spectral data. The addition of a monitoring system of this type to the input stream of a plutonium-purification cycle along with other suitable monitors on the waste streams and on the product stream provides the basis for a near real-time materials control and inventory system. Results of the laboratory-evaluation program employing plutonium in solutions with isotopic compositions typical of those involved in processing light water reactor fuels are presented. The detailed design of a monitoring cell and detection system is given. The precision and accuracy of the results relative to those measured by mass spectrometry and controlled potential coulometry are also summarized

Plutonium controversy

International Nuclear Information System (INIS)

Richmond, C.R.

1980-01-01

The toxicity of plutonium is discussed, particularly in relation to controversies surrounding the setting of radiation protection standards. The sources, amounts of, and exposure pathways of plutonium are given and the public risk estimated

Perspective on plutonium

International Nuclear Information System (INIS)

Sun, L.S.

1993-01-01

This paper is intended as a brief overview on the element plutonium. Plutonium is the first primarily man-made element to play a significant role not only in technological development, but also in the economic growth of many countries. The importance of plutonium centers around its enormous energy making it ideal for wide-scale use in reactors, while the nuclear industry continues to work toward improving safety and efficiency of plutonium as a reactor fuel politicians and the public still debate over the safety and benefits of nuclear power. (30 refs.)

Plutonium controversy

Energy Technology Data Exchange (ETDEWEB)

Richmond, C.R.

1980-01-01

The toxicity of plutonium is discussed, particularly in relation to controversies surrounding the setting of radiation protection standards. The sources, amounts of, and exposure pathways of plutonium are given and the public risk estimated. (ACR)

Safe disposal of surplus plutonium

Science.gov (United States)

Gong, W. L.; Naz, S.; Lutze, W.; Busch, R.; Prinja, A.; Stoll, W.

2001-06-01

About 150 tons of weapons grade and weapons usable plutonium (metal, oxide, and in residues) have been declared surplus in the USA and Russia. Both countries plan to convert the metal and oxide into mixed oxide fuel for nuclear power reactors. Russia has not yet decided what to do with the residues. The US will convert residues into a ceramic, which will then be over-poured with highly radioactive borosilicate glass. The radioactive glass is meant to provide a deterrent to recovery of plutonium, as required by a US standard. Here we show a waste form for plutonium residues, zirconia/boron carbide (ZrO 2/B 4C), with an unprecedented combination of properties: a single, radiation-resistant, and chemically durable phase contains the residues; billion-year-old natural analogs are available; and criticality safety is given under all conceivable disposal conditions. ZrO 2/B 4C can be disposed of directly, without further processing, making it attractive to all countries facing the task of plutonium disposal. The US standard for protection against recovery can be met by disposal of the waste form together with used reactor fuel.

Plutonium, nuclear fuel; Le plutonium, combustible nucleaire

Energy Technology Data Exchange (ETDEWEB)

Grison, E [Commissariat a l' Energie Atomique, Fontenay aux Roses (France). Centre d' Etudes Nucleaires, Saclay

1960-07-01

A review of the physical properties of metallic plutonium, its preparation, and the alloys which it forms with the main nuclear metals. Appreciation of its future as a nuclear fuel. (author) [French] Apercu sur les proprietes physiques du plutonium metallique, sa preparation, ses alliages avec les principaux metaux nucleaires. Consideration sur son avenir en tant que combustible nucleaire. (auteur)

Standard test method for plutonium assay by plutonium (III) diode array spectrophotometry

CERN Document Server

American Society for Testing and Materials. Philadelphia

2002-01-01

1.1 This test method describes the determination of total plutonium as plutonium(III) in nitrate and chloride solutions. The technique is applicable to solutions of plutonium dioxide powders and pellets (Test Methods C 697), nuclear grade mixed oxides (Test Methods C 698), plutonium metal (Test Methods C 758), and plutonium nitrate solutions (Test Methods C 759). Solid samples are dissolved using the appropriate dissolution techniques described in Practice C 1168. The use of this technique for other plutonium-bearing materials has been reported (1-5), but final determination of applicability must be made by the user. The applicable concentration range for plutonium sample solutions is 10–200 g Pu/L. 1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropria...

Surplus plutonium disposition draft environmental impact statement. Volume 2

International Nuclear Information System (INIS)

1998-07-01

vitrification process; Fast Flux Test Facility; facility data; impact assessment methods; air quality; waste management; socioeconomics; human health risks; facility accidents; evaluation of human health effects from transportation; analysis of environmental justice; and plutonium polishing

Extrinsic and intrinsic complexities of the Los Alamos Plutonium Processing Facility

International Nuclear Information System (INIS)

Bearse, R.C.; Longmire, V.L.; Roberts, N.J.

1985-01-01

Analysis of the data obtained in one year of plutonium accounting at Los Alamos reveals significant complexity. Much of this complexity arises from the complexity of the processes themselves. Additional complexity is induced by errors in the data entry process. It is important to note that there is no evidence that this complexity is adversely affecting the accounting in the plant. We have been analyzing transaction data from fiscal year 1983 processing. This study involved 62,595 transactions. The data have been analyzed using the relational database program INGRES on a VAX 11/780 computer. This software allows easy manipulation of the original data and subsets drawn from it. We have been attempting for several years to understand the global features of the TA-55 accounting data. This project has underscored several of the system's complexities. Examples that will be reported here include audit trails, lot-name multiplicity, etc

Wastes from plutonium conversion and scrap recovery operations

Energy Technology Data Exchange (ETDEWEB)

Christensen, D.C.; Bowersox, D.F.; McKerley, B.J.; Nance, R.L.

1988-03-01

This report deals with the handling of defense-related wastes associated with plutonium processing. It first defines the different waste categories along with the techniques used to assess waste content. It then discusses the various treatment approaches used in recovering plutonium from scrap. Next, it addresses the various waste management approaches necessary to handle all wastes. Finally, there is a discussion of some future areas for processing with emphasis on waste reduction. 91 refs., 25 figs., 4 tabs.

Wastes from plutonium conversion and scrap recovery operations

International Nuclear Information System (INIS)

Christensen, D.C.; Bowersox, D.F.; McKerley, B.J.; Nance, R.L.

1988-03-01

This report deals with the handling of defense-related wastes associated with plutonium processing. It first defines the different waste categories along with the techniques used to assess waste content. It then discusses the various treatment approaches used in recovering plutonium from scrap. Next, it addresses the various waste management approaches necessary to handle all wastes. Finally, there is a discussion of some future areas for processing with emphasis on waste reduction. 91 refs., 25 figs., 4 tabs

The uranium-plutonium breeder reactor fuel cycle

International Nuclear Information System (INIS)

Salmon, A.; Allardice, R.H.

1979-01-01

All power-producing systems have an associated fuel cycle covering the history of the fuel from its source to its eventual sink. Most, if not all, of the processes of extraction, preparation, generation, reprocessing, waste treatment and transportation are involved. With thermal nuclear reactors more than one fuel cycle is possible, however it is probable that the uranium-plutonium fuel cycle will become predominant; in this cycle the fuel is mined, usually enriched, fabricated, used and then reprocessed. The useful components of the fuel, the uranium and the plutonium, are then available for further use, the waste products are treated and disposed of safely. This particular thermal reactor fuel cycle is essential if the fast breeder reactor (FBR) using plutonium as its major fuel is to be used in a power-producing system, because it provides the necessary initial plutonium to get the system started. In this paper the authors only consider the FBR using plutonium as its major fuel, at present it is the type envisaged in all, current national plans for FBR power systems. The corresponding fuel cycle, the uranium-plutonium breeder reactor fuel cycle, is basically the same as the thermal reactor fuel cycle - the fuel is used and then reprocessed to separate the useful components from the waste products, the useful uranium and plutonium are used again and the waste disposed of safely. However the details of the cycle are significantly different from those of the thermal reactor cycle. (Auth.)

Demolition of Building 12, an old plutonium filter facility

International Nuclear Information System (INIS)

Christensen, E.L.; Garde, R.; Valentine, A.M.

1975-01-01

This report discusses the decommissioning and disposal of a plutonium-contaminated air filter facility that provided ventilation for the main plutonium processing plant at Los Alamos from 1945 until 1973. The health physics, waste management, and environmental aspects of the demolition are also discussed

Plutonium storage criteria

Energy Technology Data Exchange (ETDEWEB)

Chung, D. [Scientech, Inc., Germantown, MD (United States); Ascanio, X. [Dept. of Energy, Germantown, MD (United States)

1996-05-01

The Department of Energy has issued a technical standard for long-term (>50 years) storage and will soon issue a criteria document for interim (<20 years) storage of plutonium materials. The long-term technical standard, {open_quotes}Criteria for Safe Storage of Plutonium Metals and Oxides,{close_quotes} addresses the requirements for storing metals and oxides with greater than 50 wt % plutonium. It calls for a standardized package that meets both off-site transportation requirements, as well as remote handling requirements from future storage facilities. The interim criteria document, {open_quotes}Criteria for Interim Safe Storage of Plutonium-Bearing Solid Materials{close_quotes}, addresses requirements for storing materials with less than 50 wt% plutonium. The interim criteria document assumes the materials will be stored on existing sites, and existing facilities and equipment will be used for repackaging to improve the margin of safety.

Los Alamos DP West Plutonium Facility decontamination project, 1978-1981

International Nuclear Information System (INIS)

Garde, R.; Cox, E.J.; Valentine, A.M.

1982-09-01

The DP West Plutonium Facility operated by the Los Alamos National Laboratory, Los Alamos, New Mexico was decontaminated between April 1978 and April 1981. The facility was constructed in 1944 to 1945 to produce plutonium metal and fabricate parts for nuclear weapons. It was continually used as a plutonium processing and research facility until mid-1978. Decontamination operations included dismantling and removing gloveboxes and conveyor tunnels; removing process systems, utilities, and exhaust ducts; and decontaminating all remaining surfaces. This report describes glovebox and conveyor tunnel separations, decontamination techniques, health and safety considerations, waste management procedures, and costs of the operation

Dissolution of aerosol particles collected from nuclear facility plutonium production process

International Nuclear Information System (INIS)

Ning Xu; Martinez, Alex; Schappert, Michael; Montoya, D.P.; Martinez, Patrick; Tandon, Lav

2016-01-01

A simple, robust analytical chemistry method has been developed to dissolve plutonium containing particles in a complex matrix. The aerosol particles collected on Marple cascade impactor substrates were shown to be dissolved completely with an acid mixture of 12 M HNO 3 and 0.1 M HF. A pressurized closed vessel acid digestion technique was utilized to heat the samples at 130 deg C for 16 h to facilitate the digestion. The dissolution efficiency for plutonium particles was 99 %. The resulting particle digestate solution was suitable for trace elemental analysis and isotope composition determination, as well as radiochemistry measurements. (author)

Toxicology of plutonium

International Nuclear Information System (INIS)

Bair, W.J.

1974-01-01

Data are reviewed from studies on the toxicity of Pu in experimental animals. Of the several plutonium isotopes, only 238 Pu and 239 Pu have been studied well. Sufficient results have been obtained to show that the behavior of 238 Pu in biological systems and the resulting biological effects cannot be precisely predicted from studies of 239 Pu. This probably applies also to other radiologically important plutonium isotopes which have half-lives ranging from 45 days to 10 7 years and decay by β-emission, electron capture, and spontaneous fission, as well as by emission of α-particles. All the biological effects of plutonium described in this review are attributed to alpha-particle radiation emitted by the plutonium. However, since plutonium is a chemically active heavy metal, one cannot ignore the possibility of chemical toxicity of the low-specific-activity isotopes, 239 Pu, 242 Pu, and 244 Pu. The preponderance of our knowledge of plutonium toxicology has come from short-term studies of relatively high dosage levels in several animal species. The consequences of high-level internal exposures can be predicted with confidence in experimental animals and probably also in man. However, considering the care with which plutonium is handled in the nuclear industry, a high-level contamination event is unlikely. Considerably less is known about the long-term effects of low levels of contamination. (250 references) (U.S.)

Cycle downstream: the plutonium question; Aval du cycle la question du plutonium

Energy Technology Data Exchange (ETDEWEB)

Zask, G [Electricite de France, EDF/DAC, 75 - Paris (France); Rome, M [Electricite de France, EDF, Service Etudes et Projets Thermiques et Nucleaires, 92 - Courbevoie (France); Delpech, M [CEA Cadarache, Dept. d' Etudes des Reacteurs/SPRC, 13 - Saint-Paul-lez-Durance (France); and others

1998-06-29

This day, organized by the SFEN, took place at Paris the 4 june 1998. Nine papers were presented. They take stock on the plutonium physics and its utilization as a nuclear fuel. This day tried to bring information to answer the following questions: do people have to keep the plutonium in the UOX fuel or in the MOX fuel in order to use it for future fast reactors? Do people have to continue obstinately the plutonium reprocessing in the MOX for the PWR type reactors? Will it be realized a underground disposal? Can it be technically developed plutonium incinerators and is it economically interesting? The plutonium physics, the experimental programs and the possible solutions are presented. (A.L.B.)

Separation of neptunium from uranium and plutonium in the Purex process

International Nuclear Information System (INIS)

Kolarik, Z.; Schuler, R.

1984-01-01

The possibility of removing neptunium from the Purex process in the first extraction cycle was investigated. Butyraldehyde was found to reduce Np(VI) to Np(V), but not Pu(IV) to Pu(III). Up to 99.7% Np can be separated from uranium and plutonium in the 1A extractor or, much more favourably, in an additional partitioning extractor. Hydroxylamine nitrate can be used for reducing Np(VI) to Np(V) in a uranium purification cycle at a high U concentration in the feed solution. Here the decontamination factor for Np can be as high as 2300 and is lowered if iron is present in the feed. (author)

Transplutonium elements production program: extraction chromatographic process for plutonium irradiated targets

International Nuclear Information System (INIS)

Bourges, J.; Madic, C.; Koehly, G.

1980-01-01

The treatment of irradiated plutonium targets by extraction chromatography allowed the purification of the isotopes 243 Am and 244 Cm on the scale of few tens of grams. This process proved to be extremely simple and flexible, and yielded results which are reproducible in time. The chief advantage of the TBP process over the HDEHP process in high and medium activity conditions lies in the rapid absorption/desorption kinetics of the elements to be purified and in the separation of americium from curium, which largely offsets its lower selectivity for lanthanide elements. it is certainly possible to improve the performance of this process by: a) optimization of the characteristics of the stationary phase, b) improvement in the filling technique and in hydraulic operation of the columns, c) on-line analysis of americium (the key element in actinide/lanthanide separation) in the eluate. The application of extraction chromatography with HD(DiBM)P to the purification of 243 Am of the end of treatment makes the process more consistent, eliminates the delicate stages implemented in hot cell, and considerably improves final product quality

Plutonium - its behavior in natural-water systems and assimilation by man

International Nuclear Information System (INIS)

Larsen, R.P.; Nelson, D.M.; Bhattacharyya, M.H.; Oldham, R.D.

1981-01-01

There are a number of factors which must be considered in establishing whether or not the inadvertent intrusion of a sizable amount of plutonium-bearing material into a natural-water system may have a significant impact on the health of those individuals who use that system as a drinking-water resource. These factors include the chemical form(s) and solubility of plutonium in natural waters, its behavior in relation to natural processes (geochemical and biological), its fate in water-treatment systems, and its uptake by man from drinking water. From the results obtained of the behavior in natural-water systems, it appears that (1) the chemical forms of plutonium dissolved in natural waters are Pu(IV) and Pu(V), (2) the soluble plutonium in many waters is bound to the organic constituents which probably enhance plutonium solubility, (3) the natural process responsible for the removal of plutonium from water is adsorption onto sediments, and (4) in water-treatment systems, soluble plutonium is oxidized to the VI state and this form is not removed. From investigations of gastrointestinal absorption, it appears that the value for f 1 , the fraction transferred from the gut to blood, is greater than 1 x 10 - 3 and may be as high as 2 x 10 - 1

Technical report for generic site add-on facility for plutonium polishing

International Nuclear Information System (INIS)

1998-06-01

The purpose of this report is to provide environmental data and reference process information associated with incorporating plutonium polishing steps (dissolution, impurity removal, and conversion to oxide powder) into the genetic-site Mixed-Oxide Fuel Fabrication Facility (MOXFF). The incorporation of the plutonium polishing steps will enable the removal of undesirable impurities, such as gallium and americium, known to be associated with the plutonium. Moreover, unanticipated impurities can be removed, including those that may be contained in (1) poorly characterized feed materials, (2) corrosion products added from processing equipment, and (3) miscellaneous materials contained in scrap recycle streams. These impurities will be removed to the extent necessary to meet plutonium product purity specifications for MOX fuels. Incorporation of the plutonium polishing steps will mean that the Pit Disassembly and Conversion Facility (PDCF) will need to produce a plutonium product that can be dissolved at the MOXFF in nitric acid at a suitable rate (sufficient to meet overall production requirements) with the minimal usage of hydrofluoric acid, and its complexing agent, aluminum nitrate. This function will require that if the PDCF product is plutonium oxide powder, that powder must be produced, stored, and shipped without exceeding a temperature of 600 C

Plutonium recovery from spent reactor fuel by uranium displacement

Science.gov (United States)

Ackerman, J.P.

1992-03-17

A process is described for separating uranium values and transuranic values from fission products containing rare earth values when the values are contained together in a molten chloride salt electrolyte. A molten chloride salt electrolyte with a first ratio of plutonium chloride to uranium chloride is contacted with both a solid cathode and an anode having values of uranium and fission products including plutonium. A voltage is applied across the anode and cathode electrolytically to transfer uranium and plutonium from the anode to the electrolyte while uranium values in the electrolyte electrolytically deposit as uranium metal on the solid cathode in an amount equal to the uranium and plutonium transferred from the anode causing the electrolyte to have a second ratio of plutonium chloride to uranium chloride. Then the solid cathode with the uranium metal deposited thereon is removed and molten cadmium having uranium dissolved therein is brought into contact with the electrolyte resulting in chemical transfer of plutonium values from the electrolyte to the molten cadmium and transfer of uranium values from the molten cadmium to the electrolyte until the first ratio of plutonium chloride to uranium chloride is reestablished.

Plutonium recovery from spent reactor fuel by uranium displacement

International Nuclear Information System (INIS)

Ackerman, J.P.

1992-01-01

A process is described for separating uranium values and transuranic values from fission products containing rare earth values when the values are contained together in a molten chloride salt electrolyte. A molten chloride salt electrolyte with a first ratio of plutonium chloride to uranium chloride is contacted with both a solid cathode and an anode having values of uranium and fission products including plutonium. A voltage is applied across the anode and cathode electrolytically to transfer uranium and plutonium from the anode to the electrolyte while uranium values in the electrolyte electrolytically deposit as uranium metal on the solid cathode in an amount equal to the uranium and plutonium transferred from the anode causing the electrolyte to have a second ratio of plutonium chloride to uranium chloride. Then the solid cathode with the uranium metal deposited thereon is removed and molten cadmium having uranium dissolved therein is brought into contact with the electrolyte resulting in chemical transfer of plutonium values from the electrolyte to the molten cadmium and transfer of uranium values from the molten cadmium to the electrolyte until the first ratio of plutonium chloride to uranium chloride is reestablished

The handling of plutonium hexafluoride (1962); Manipulation de l'hexafluorure de plutonium (1962)

Energy Technology Data Exchange (ETDEWEB)

Berard, Ph [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

1961-11-15

The major problem posed in this work is the instability of plutonium hexafluoride. The influence of various factors on the decomposition of the fluoride has been studied: physical aspect of the walls, nature of the metal and its pretreatment, influence of the temperature. A means of detecting plutonium-239 in a metallic apparatus by {gamma}-ray counting has been developed; the sensitivity is of the order of half a milligram, but the precision is very low (about 50 per cent). Yields of over 95 per cent have been obtained for the transfer of plutonium during the preparation and sublimation of the hexafluoride. This study confirms the possibility of using plutonium hexafluoride for the extraction of plutonium from irradiated fuel elements by a dry method. (author) [French] Le probleme majeur de cette etude a ete l'instabilite de l'hexafluorure de plutonium. Nous avons etudie l'influence de divers facteurs sur la decomposition de l'hexafluorure: aspect physique des parois, nature du metal et de son pretraitement, influence de la temperature. Nous avons mis au point un mode de detection du plutonium-239 dans un appareillage metallique par comptage du rayonnement {gamma}; la sensibilite est de l'ordre du demi-milligramme, mais la precision est tres faible (50 pour cent environ). Nous avons obtenu des rendements depassant 95 pour cent dans le transfert du plutonium au cours de la fabrication et de la sublimation de l'hexafluorure. Cette etude confirme la possibilite d'utiliser l'hexafluorure de plutonium dans l'extraction du plutonium des combustibles irradies par voie seche. (auteur)

Plutonium in a grassland ecosystem

International Nuclear Information System (INIS)

Little, C.A.

1976-01-01

This study was concerned with plutonium contamination of grassland at the U.S. Energy Research and Development Administration Rocky Flats plant northwest of Denver, Colorado. Of interest were: the definition of major plutonium-containing ecosystem compartments; the relative amounts in those compartments; how those values related to studies done in other geogrphical areas; whether or not the predominant isotopes, 238 Pu and 239 Pu, behaved differently; and what mechanisms might have allowed for the observed patterns of contamination. Samples of soil, litter, vegetation, arthropods, and small mammals were collected for plutonium analysis and mass determination from each of two macroplots. Small aliquots (5 g or less) were analyzed by a rapid liquid scintillation technique and by alpha spectrometry. Of the compartments sampled, greater than 99% of the total plutonium was contained in the soil. The concentrations of plutonium in soil were significantly inversely correlated with distance from the contamination source, depth of the sample, and particle size of the sieved soil samples. The soil data suggested that the distribution of contamination largely resulted from physical transport processes. A mechanism of agglomerated submicron plutonium oxide particles and larger (1-500 μm) host soil particles was proposed. Concentrations of Pu in litter and vegetation were inversely correlated to distance from the source and directly correlated to soil concentrations at the same location. Comparatively high concentration ratios of vegetation to soil suggested wind resuspension of contamination as an important transport mechanism. Arthropod and small mammal samples were highly skewed, kurtotic, and quite variable, having coefficients of variation (standard deviation/mean) as high as 600%. Bone Pu concentrations were lower than other tissues. Hide, GI, and lung were generally not higher in Pu than kidney, liver and muscle

Preparation of plutonium hexafluoride. Recovery of plutonium from waste dross (1962)

International Nuclear Information System (INIS)

Gendre, R.

1962-01-01

The object of this work is to study the influence of various physical factors on the rate of fluorination of solid plutonium tetrafluoride by fluorine. In a horizontal oven with a circulation for pure fluorine at atmospheric pressure and 520 deg. C, at a fluorine rate of 9 litres/hour, it is possible to transform 3 g of tetrafluoride to hexafluoride with about 100 per cent transformation and a recovery yield of over 90 per cent, in 4 to 5 hours. The fluorination rate is a function of the temperature, of the fluorine flow-rate, of the crucible surface, of the depth of the tetrafluoride layer and of the reaction time. It does not depend on the diffusion of the fluorine into the solid but is determined by the reaction at the gas-solid interface and obeys the kinetic law (1 - T T ) 1/3 = kt + 1. The existence of intermediate fluorides, in particular Pu 4 F 17 , is confirmed by a break in the Arrhenius plot at about 370 deg. C, by differences in the fluorination rates inside the tetrafluoride layer, and by reversible colour changes. The transformation to hexafluoride occurs with a purification with respect of the foreign elements present in the initial plutonium. Recovery of plutonium from waste dross: The study is based on the transformation of occluded plutonium particles to gaseous hexafluoride which is then decomposed thermally to the tetrafluoride which can be reintroduced directly in the production circuit. Under the conditions considered this process is not applicable industrially. After milling, it is possible to separate the dross into enriched (75 per cent Pu in 2.6 per cent by weight of dross) and depleted portions. By prolonged fluorination (16 hours) of the various fractions it is possible to recover about 80 per cent of the plutonium. A treatment plant using fluidization, as described at the end of this study, should make it possible to substantially improve the yield. (author) [fr

Plutonium re-cycle in HTR

Energy Technology Data Exchange (ETDEWEB)

Desoisa, J. A.

1974-03-15

The study of plutonium cycles in HTRs using reprocessed plutonium from Magnox and AGR fuel cycles has shown that full core plutonium/uranium loadings are in general not feasible, burn-up is limited due the need for lower loadings of plutonium to meet reload core reactivity limits, on-line refueling is not practicable due to the need for higher burnable poison loadings, and low conversion rates in the plutonium-uranium cycles cannot be mitigated by axial loading schemes so that fissile make-up is needed if HTR plutonium recycle is desired.

PLUTONIUM-ZIRCONIUM ALLOYS

Science.gov (United States)

Schonfeld, F.W.; Waber, J.T.

1960-08-30

A series of nuclear reactor fuel alloys consisting of from about 5 to about 50 at.% zirconium (or higher zirconium alloys such as Zircaloy), balance plutonium, and having the structural composition of a plutonium are described. Zirconium is a satisfactory diluent because it alloys readily with plutonium and has desirable nuclear properties. Additional advantages are corrosion resistance, excellent fabrication propenties, an isotropie structure, and initial softness.

Plutonium-uranium separation in the Purex process using mixtures of hydroxylamine nitrate and ferrous sulfamate

International Nuclear Information System (INIS)

McKibben, J.M.; Chostner, D.F.; Orebaugh, E.G.

1983-11-01

Laboratory studies, followed by plant operation, established that a mixture of hydroxylamine nitrate (HAN) and ferrous sulfamate (FS) is superior to FS used alone as a reductant for plutonium in the Purex first cycle. FS usage has been reduced by about 70% (from 0.12 to 0.04M) compared to the pre-1978 period. This reduced the volume of neutralized waste due to FS by 194 liters/metric ton of uranium (MTU) processed. The new flowsheet also gives lower plutonium losses to waste and at least comparable fission product decontamination. To achieve satisfactory performance at this low concentration of FS, the acidity in the 1B mixer-settler was reduced by using a split-scrub - a low acid scrub in stage one and a higher acid scrub in stage three - to remove acid from the solvent exiting the 1A centrifugal contactor. 8 references, 14 figures, 1 table

The use of plutonium in Swedish reactors

International Nuclear Information System (INIS)

Forsstroem, H.

1982-09-01

The report deals with the utilization of plutonium in Swedish nuclear power plants. The plutonium content of the mixed oxide fuel will normally be 3-7 per cent. The processing of spent nuclear fuel will produce about 6 ton plutonium. The use of mixed oxide fuel in Forsmark 3 and Oskarshamn 3 is discussed. The fuel cycle will start with the manufacturing of the fuel elements abroad and proceeds with transport and utilization, storing of spent fuel about 40 years in Sweden followed by direct disposal. The manufacture and use of mixed oxide (MOX) fuel is based on well-known techniques. Approximately 20 000 MOX fuel rods have been irradiated and the fuel is essentially equivalent to uranium oxide fuel. 30-50 per cent of the core may be composed of MOX-fuel without any effect on the operation and safety of the reactor which has been originally designed for uranium fuel. The evaluation of international fuel cycle (INFCE) states that the proliferation risks are very small. The recycling of plutonium will reduce demand for enriched uranium and the calculations show that 6.3 ton plutonium will replace the enrichment of 600 ton natural uranium. (G.B.)

Preparation of plutonium hexafluoride. Recovery of plutonium from waste dross (1962); Preparation de l'hexafluorure de plutonium. Recuperation du plutonium des scories d'elaboration (1962)

Energy Technology Data Exchange (ETDEWEB)

Gendre, R [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1962-07-01

The object of this work is to study the influence of various physical factors on the rate of fluorination of solid plutonium tetrafluoride by fluorine. In a horizontal oven with a circulation for pure fluorine at atmospheric pressure and 520 deg. C, at a fluorine rate of 9 litres/hour, it is possible to transform 3 g of tetrafluoride to hexafluoride with about 100 per cent transformation and a recovery yield of over 90 per cent, in 4 to 5 hours. The fluorination rate is a function of the temperature, of the fluorine flow-rate, of the crucible surface, of the depth of the tetrafluoride layer and of the reaction time. It does not depend on the diffusion of the fluorine into the solid but is determined by the reaction at the gas-solid interface and obeys the kinetic law (1 - T{sub T}){sup 1/3} = kt + 1. The existence of intermediate fluorides, in particular Pu{sub 4} F{sub 17}, is confirmed by a break in the Arrhenius plot at about 370 deg. C, by differences in the fluorination rates inside the tetrafluoride layer, and by reversible colour changes. The transformation to hexafluoride occurs with a purification with respect of the foreign elements present in the initial plutonium. Recovery of plutonium from waste dross: The study is based on the transformation of occluded plutonium particles to gaseous hexafluoride which is then decomposed thermally to the tetrafluoride which can be reintroduced directly in the production circuit. Under the conditions considered this process is not applicable industrially. After milling, it is possible to separate the dross into enriched (75 per cent Pu in 2.6 per cent by weight of dross) and depleted portions. By prolonged fluorination (16 hours) of the various fractions it is possible to recover about 80 per cent of the plutonium. A treatment plant using fluidization, as described at the end of this study, should make it possible to substantially improve the yield. (author) [French] L'objet de l'etude est l'influence des differents

Optimization and plutonium equilibrium

International Nuclear Information System (INIS)

Silver, G.L.

1976-01-01

The sequential simplex method has been used to estimate the extent of disproportionation of tetravalent plutonium in dilute acid. A method for simulating potentiometric titrations is proposed, and this method suggests that the stoichiometric end point and the inflection point may not always correspond in the potentiometric titration of plutonium. A possible characteristic equation for the nitrite-plutonium reaction is illustrated, and the method of proportional equations is extended to the iron-plutonium reaction

Assesment of Plutonium 238 and Plutonium 239+240 in soils of different agricultural regions of Guatemala

International Nuclear Information System (INIS)

Gutierrez Martinez, E.A.

1998-02-01

In this report an assesment and measurement of PLUTONIUM 238, PLUTONIUM 239, and PLUTONIUM 240 are made. Samples of cultivated soils in 15 provinces of Guatemala were taken. To separate plutonium isotopes a radiochemical method was made using extraction, precipitation and ionic interchange. By electrodeposition the plutonium was measured using an alpha spectroscopy by PIPS method. The radioactivity ranges from 2.84 mBq/Kg to 36.38 mBq/Kg for plutonium 238, and 8.46 mBq/Kg to 26.61 mBq/Kg for plutonium 239+240

Pyrochemical investigations into recovering plutonium from americium extraction salt residues

International Nuclear Information System (INIS)

Fife, K.W.; West, M.H.

1987-05-01

Progress into developing a pyrochemical technique for separating and recovering plutonium from spent americium extraction waste salts has concentrated on selective chemical reduction with lanthanum metal and calcium metal and on the solvent extraction of americium with calcium metal. Both techniques are effective for recovering plutonium from the waste salt, although neither appears suitable as a separation technique for recycling a plutonium stream back to mainline purification processes. 17 refs., 13 figs., 2 tabs

Reduction of uranium and plutonium oxides by aluminum. Application to the recycling of plutonium; Reduction des oxydes d'uranium et de plutonium par l'aluminium application au recyclage du plutonium

Energy Technology Data Exchange (ETDEWEB)

Gallay, J [Commissariat a l' Energie Atomique, Valduc (France). Centre d' Etudes

1968-07-01

A process for treating plutonium oxide calcined at high temperatures (1000 to 2000 deg. C) with a view to recovering the metal consists in the reduction of this oxide dissolved in a mixture of aluminium, sodium and calcium fluorides by aluminium at about 1180 deg. C. The first part of the report presents the results of reduction tests carried out on the uranium oxides UO{sub 2} and U{sub 3}O{sub 8}; these are in agreement with the thermodynamic calculations of the exchange reaction at equilibrium. The second part describes the application of this method to plutonium oxides. The Pu-Al alloy obtained (60 per cent Pu) is then recycled in an aqueous medium. (author) [French] Un procede de traitement de l'oxyde de plutonium calcine a haute temperature (1000 deg. C a 2000 deg. C), en vue de la recuperation du metal, consiste a reduire cet oxyde dissous dans un melange de fluorures d'aluminium, de sodium et de calcium, par l'aluminium vers 1180 deg. C. Une premiere partie du rapport presente les resultats des essais de reduction des oxydes d'uranium UO{sub 2} et U{sub 3}O{sub 8}, en accord avec les resultats du calcul thermodynamique de la reaction d'echange a l'equilibre. Une seconde partie rend compte de l'application de cette methode a l'oxyde de plutonium. L'alliage Pu-Al obtenu (60 pour cent Pu) est ensuite recycle par voie aqueuse. (auteur)

Evolutionary/advanced light water reactor data report

Energy Technology Data Exchange (ETDEWEB)

NONE

1996-02-09

The US DOE Office of Fissile Material Disposition is examining options for placing fissile materials that were produced for fabrication of weapons, and now are deemed to be surplus, into a condition that is substantially irreversible and makes its use in weapons inherently more difficult. The principal fissile materials subject to this disposition activity are plutonium and uranium containing substantial fractions of plutonium-239 uranium-235. The data in this report, prepared as technical input to the fissile material disposition Programmatic Environmental Impact Statement (PEIS) deal only with the disposition of plutonium that contains well over 80% plutonium-239. In fact, the data were developed on the basis of weapon-grade plutonium which contains, typically, 93.6% plutonium-239 and 5.9% plutonium-240 as the principal isotopes. One of the options for disposition of weapon-grade plutonium being considered is the power reactor alternative. Plutonium would be fabricated into mixed oxide (MOX) fuel and fissioned (``burned``) in a reactor to produce electric power. The MOX fuel will contain dioxides of uranium and plutonium with less than 7% weapon-grade plutonium and uranium that has about 0.2% uranium-235. The disposition mission could, for example, be carried out in existing power reactors, of which there are over 100 in the United States. Alternatively, new LWRs could be constructed especially for disposition of plutonium. These would be of the latest US design(s) incorporating numerous design simplifications and safety enhancements. These ``evolutionary`` or ``advanced`` designs would offer not only technological advances, but also flexibility in siting and the option of either government or private (e.g., utility) ownership. The new reactor designs can accommodate somewhat higher plutonium throughputs. This data report deals solely with the ``evolutionary`` LWR alternative.

Evolutionary/advanced light water reactor data report

International Nuclear Information System (INIS)

1996-01-01

The US DOE Office of Fissile Material Disposition is examining options for placing fissile materials that were produced for fabrication of weapons, and now are deemed to be surplus, into a condition that is substantially irreversible and makes its use in weapons inherently more difficult. The principal fissile materials subject to this disposition activity are plutonium and uranium containing substantial fractions of plutonium-239 uranium-235. The data in this report, prepared as technical input to the fissile material disposition Programmatic Environmental Impact Statement (PEIS) deal only with the disposition of plutonium that contains well over 80% plutonium-239. In fact, the data were developed on the basis of weapon-grade plutonium which contains, typically, 93.6% plutonium-239 and 5.9% plutonium-240 as the principal isotopes. One of the options for disposition of weapon-grade plutonium being considered is the power reactor alternative. Plutonium would be fabricated into mixed oxide (MOX) fuel and fissioned (''burned'') in a reactor to produce electric power. The MOX fuel will contain dioxides of uranium and plutonium with less than 7% weapon-grade plutonium and uranium that has about 0.2% uranium-235. The disposition mission could, for example, be carried out in existing power reactors, of which there are over 100 in the United States. Alternatively, new LWRs could be constructed especially for disposition of plutonium. These would be of the latest US design(s) incorporating numerous design simplifications and safety enhancements. These ''evolutionary'' or ''advanced'' designs would offer not only technological advances, but also flexibility in siting and the option of either government or private (e.g., utility) ownership. The new reactor designs can accommodate somewhat higher plutonium throughputs. This data report deals solely with the ''evolutionary'' LWR alternative

Materials selection of surface coatings in an advanced size reduction facility

International Nuclear Information System (INIS)

Briggs, J.L.; Younger, A.F.

1980-01-01

A materials selection test program was conducted to characterize optimum interior surface coatings for an advanced size reduction facility. The equipment to be processed by this facility consists of stainless steel apparatus (e.g., glove boxes, piping, and tanks) used for the chemical recovery of plutonium. Test results showed that a primary requirement for a satisfactory coating is ease of decontamination. A closely related concern is the resistance of paint films to nitric acid - plutonium environments. A vinyl copolymer base paint was the only coating, of eight paints tested, with properties that permitted satisfactory decontamination of plutonium and also performed equal to or better than the other paints in the chemical resistance, radiation stability, and impact tests

The PWI [plutonium waste incinerator] expert system: Real time, PC-based process analysis

International Nuclear Information System (INIS)

Brown, K.G.; Smith, F.G.

1987-01-01

A real time, microcomputer-based expert system is being developed for a prototype plutonium waste incinerator (PWI) process at Du Pont's Savannah River Laboratory. The expert system will diagnose instrumentation problems, assist operator training, serve as a repository for engineering knowledge about the process, and provide continuous operation and performance information. A set of necessary operational criteria was developed from process and engineering constraints; it was used to define hardware and software needs. The most important criterion is operating speed because the analysis operates in real time. TURBO PROLOG by Borland International was selected. The analysis system is divided into three sections: the user-system interface, the inference engine and rule base, and the files representing the blackboard information center

Electrochemical studies on plutonium in molten salts

International Nuclear Information System (INIS)

Bourges, G.; Lambertin, D.; Rochefort, S.; Delpech, S.; Picard, G.

2007-01-01

Electrochemical studies on plutonium have been supporting the development of pyrochemical processes involving plutonium at CEA. The electrochemical properties of plutonium have been studied in molten salts - ternary eutectic mixture NaCl-KCl-BaCl 2 , equimolar mixture NaCl-KCl and pure CaCl 2 - and in liquid gallium at 1073 K. The formal, or apparent, standard potential of Pu(III)/Pu redox couple in eutectic mixture of NaCl-KCl-BaCl 2 at 1073 K determined by potentiometry is equal to -2.56 V (versus Cl 2 , 1 atm/Cl - reference electrode). In NaCl-KCl eutectic mixture and in pure CaCl 2 the formal standard potentials deduced from cyclic voltammetry are respectively -2.54 V and -2.51 V. These potentials led to the calculation of the activity coefficients of Pu(III) in the molten salts. Chronoamperometry on plutonium in liquid gallium using molten chlorides - CaCl 2 and equimolar NaCl/KCl - led to the determination of the activity coefficient of Pu in liquid Ga, log γ = -7.3. This new data is a key parameter to assess the thermodynamic feasibility of a process using gallium as solvent metal. By comparing gallium with other solvent metals - cadmium, bismuth, aluminum - gallium appears to be, with aluminum, more favorable for the selectivity of the separation at 1073 K of plutonium from cerium. In fact, compared with a solid tungsten electrode, none of these solvent liquid metals is a real asset for the selectivity of the separation. The role of a solvent liquid metal is mainly to trap the elements

Diffusion in the uranium - plutonium system and self-diffusion of plutonium in epsilon phase; Diffusion dans le systeme uranium-plutonium et autodiffusion du plutonium epsilon

Energy Technology Data Exchange (ETDEWEB)

Dupuy, M [Commissariat a l' Energie Atomique, Fontenay-Aux-Roses (France). Centre d' Etudes Nucleaires

1967-07-01

A survey of uranium-plutonium phase diagram leads to confirm anglo-saxon results about the plutonium solubility in {alpha} uranium (15 per cent at 565 C) and the uranium one in {zeta} phase (74 per cent at 565 C). Interdiffusion coefficients, for concentration lower than 15 per cent had been determined in a temperature range from 410 C to 640 C. They vary between 0.2 and 6 10{sup 12} cm{sup 2} s{sup -1}, and the activation energy between 13 and 20 kcal/mole. Grain boundary, diffusion of plutonium in a uranium had been pointed out by micrography, X-ray microanalysis and {alpha} autoradiography. Self-diffusion of plutonium in {epsilon} phase (bcc) obeys Arrhenius law: D = 2. 10{sup -2} exp -(18500)/RT. But this activation energy does not follow empirical laws generally accepted for other metals. It has analogies with 'anomalous' bcc metals ({beta}Zr, {beta}Ti, {beta}Hf, U{sub {gamma}}). (author) [French] Une etude du diagramme d'equilibre uranium-plutonium conduit a confirmer les resultats anglo-saxons relatifs a la solubilite du plutonium dans l'uranium {alpha} (15 pour cent a 565 C) et de l'uranium dans la phase {zeta} (74 pour cent a 565 C). Les coefficients de diffusion chimique, pour des concentrations inferieures a 15 pour cent ont ete determines a des temperatures comprises entre 410 et 640 C. Ils se situent entre 0.2 et 6. 10{sup 12} cm{sup 2} s{sup -1}. L'energie d'activation varie entre 13 et 20 kcal/mole. La diffusion intergranulaire du plutonium dans l'uranium a a ete mise en evidence par micrographie, microanalyse X et autoradiographie {alpha}. L' autodiffusion du plutonium {beta} cubique centree obeit a la loi d'Arrhenius D = 2. 10{sup -2} exp - (18500)/RT. Son energie d'activation n'obeit pas aux lois empiriques generalement admises pour les autres metaux. Elle possede des analogies avec les cubiques centres ''anormaux'' (Zr{beta}, Ti{beta}, Hf{beta}, U{gamma}). (auteur)

Direct conversion of plutonium-containing materials to borosilicate glass for storage or disposal

International Nuclear Information System (INIS)

Forsberg, C.W.; Beahm, E.C.

1995-01-01

A new process, the Glass Material Oxidation and Dissolution System (GMODS), has been invented for the direct conversion of plutonium metal, scrap, and residue into borosilicate glass. The glass should be acceptable for either the long-term storage or disposition of plutonium. Conversion of plutonium from complex chemical mixtures and variable geometries into homogeneous glass (1) simplifies safeguards and security; (2) creates a stable chemical form that meets health, safety, and environmental concerns; (3) provides an easy storage form; (4) may lower storage costs; and (5) allows for future disposition options. In the GMODS process, mixtures of metals, ceramics, organics, and amorphous solids containing plutonium are fed directly into a glass melter where they are directly converted to glass. Conventional glass melters can accept materials only in oxide form; thus, it is its ability to accept materials in multiple chemical forms that makes GMODS a unique glass making process. Initial proof-of-principle experiments have converted cerium (plutonium surrogate), uranium, stainless steel, aluminum, and other materials to glass. Significant technical uncertainties remain because of the early nature of process development

Developing a physiologically based approach for modeling plutonium decorporation therapy with DTPA.

Science.gov (United States)

Kastl, Manuel; Giussani, Augusto; Blanchardon, Eric; Breustedt, Bastian; Fritsch, Paul; Hoeschen, Christoph; Lopez, Maria Antonia

2014-11-01

To develop a physiologically based compartmental approach for modeling plutonium decorporation therapy with the chelating agent Diethylenetriaminepentaacetic acid (Ca-DTPA/Zn-DTPA). Model calculations were performed using the software package SAAM II (©The Epsilon Group, Charlottesville, Virginia, USA). The Luciani/Polig compartmental model with age-dependent description of the bone recycling processes was used for the biokinetics of plutonium. The Luciani/Polig model was slightly modified in order to account for the speciation of plutonium in blood and for the different affinities for DTPA of the present chemical species. The introduction of two separate blood compartments, describing low-molecular-weight complexes of plutonium (Pu-LW) and transferrin-bound plutonium (Pu-Tf), respectively, and one additional compartment describing plutonium in the interstitial fluids was performed successfully. The next step of the work is the modeling of the chelation process, coupling the physiologically modified structure with the biokinetic model for DTPA. RESULTS of animal studies performed under controlled conditions will enable to better understand the principles of the involved mechanisms.

Measurement of plutonium and americium in molten salt residues

International Nuclear Information System (INIS)

Haas, F.X.; Lawless, J.L.; Herren, W.E.; Hughes, M.E.

1979-01-01

The measurement of plutonium and americium in molten salt residues using a segmented gamma-ray scanning device is described. This system was calibrated using artificially fabricated as well as process generated samples. All samples were calorimetered and the americium to plutonium content of the samples determined by gamma-ray spectroscopy. For the nine samples calorimetered thus far, no significant biases are present in the comparison of the segmented gamma-ray assay and the calorimetric assay. Estimated errors are of the order of 10 percent and is dependent on the americium to plutonium ratio determination

A method for the gravimetric determination of plutonium in pure plutonium nitrate concentrate solution

International Nuclear Information System (INIS)

Mair, M.A.; Savage, D.J.

1986-12-01

Plutonium nitrate solution is treated with sulphuric acid before being heated and finally ignited. The stoichiometric plutonium dioxide so formed is weighed and hence the plutonium content is calculated. (author)

Facility model for the Los Alamos Plutonium Facility

International Nuclear Information System (INIS)

Coulter, C.A.; Thomas, K.E.; Sohn, C.L.; Yarbro, T.F.; Hench, K.W.

1986-01-01

The Los Alamos Plutonium Facility contains more than sixty unit processes and handles a large variety of nuclear materials, including many forms of plutonium-bearing scrap. The management of the Plutonium Facility is supporting the development of a computer model of the facility as a means of effectively integrating the large amount of information required for material control, process planning, and facility development. The model is designed to provide a flexible, easily maintainable facility description that allows the faciltiy to be represented at any desired level of detail within a single modeling framework, and to do this using a model program and data files that can be read and understood by a technically qualified person without modeling experience. These characteristics were achieved by structuring the model so that all facility data is contained in data files, formulating the model in a simulation language that provides a flexible set of data structures and permits a near-English-language syntax, and using a description for unit processes that can represent either a true unit process or a major subsection of the facility. Use of the model is illustrated by applying it to two configurations of a fictitious nuclear material processing line

F. Biological hazards of plutonium

International Nuclear Information System (INIS)

1976-01-01

Plutonium is an unavoidable result of present nuclear power programmes. Its predominant isotopes are extremely long-lived and very toxic if absorbed in the body. In view of the increasing potential for plutonium and man to come into contact, the consequences of any plutonium release into the environment should be scientifically examined. This report is an attempt to place in one document a fully referenced account of the on-going work in many areas. There are three sections. Part 1 deals with the amounts of plutonium available in the fuel cycle, its properties and the probability of routine or accidental release. Part 2 examines the ways in which plutonium can reach man, in particular through food chains or inhalation. Part 3 details the biological effects of plutonium once it is absorbed into the body, assesses the amounts likely to be harmful and discusses the adequacy of present standards for plutonium burdens. There are two appendices. The likely differences between Pu-239, the most studied isotope, and other plutonium isotopes or transuranic nuclides are outlined in Appendix A. Appendix B contains a fuller account of the ways in which the fate of ingested or inhaled plutonium have been determined

Plutonium recovery from spent glass fiber paper fine air filter

International Nuclear Information System (INIS)

Rovnyj, S.I.; Guzhavin, V.I.; Pyatin, N.P.; Evlanov, D.S.

2002-01-01

Investigations into the realizing technology of plutonium recovery from waste glass paper filters of fine purification were conducted. Two process schemes involving the nitro-fluoro-acid treatment of glass paper in the mixture of nitric and hydrofluoric acids and the previous alkali treatment of glass paper with the following nitro-fluoro-acid leaching of plutonium from pulp by the mixture of nitric and hydrofluoric acids were developed. Alkali, nitrate solutions and insoluble precipitants were analyzed for plutonium content [ru

Use of plutonium for power production

International Nuclear Information System (INIS)

1965-01-01

The panel reviewed available information on various aspects of plutonium utilization, such as physics of plutonium, technology of plutonium fuels in thermal and fast reactors, behaviour of plutonium fuel under reactor irradiation, technological and economic aspects of plutonium fuel cycle. Refs, figs and tabs

World status report: plutonium

International Nuclear Information System (INIS)

Dircks, W.

1992-01-01

In a recent speech in Japan, the Deputy Director General of the International Atomic Energy Agency (IAEA) said that the economic case for reprocessing spent nuclear fuel had been severely eroded. An edited version of the speech is given. The changed prospects for nuclear energy is given as the reason why the demand for plutonium has declined sharply. The oil crisis of the 1970s reduced the demand for electric power and the economic justification for the use of recycled plutonium. The stockpile of isolated plutonium is growing rapidly giving rise to worries about its security. From this point of view, isolated plutonium is best kept in reactor fuel not separated out. In this connection the IAEA has offered to help in the storage of plutonium so that vigorous safety and security requirements are met. In Japan there is a debate about the plutonium which is dependent on the future of the fast breeder reactor programme. (UK)

Cost-benefit analysis of unfired PuO2 pellets as an alternative plutonium shipping form

International Nuclear Information System (INIS)

Mishima, J.; Brackenbush, L.W.; Libby, R.A.; Soldat, K.L.; White, G.D.

1983-10-01

A limited cost-benefit evaluation was performed concerning use of unfired plutonium dioxide pellets as a shipping form. Two specific processing operations are required for this use, one to form the pellet (pelletizing) and a second to reconstitute an acceptable powder upon receipt (reconstitution). The direct costs for the pelletizing operation are approximately $208,000 for equipment and its installation and $122 per kg of plutonium processed (based upon a 20-kg plutonium/day facility). The direct costs for reconstitution are approximately $90,000 for equipment and its installation and $81 per kg of plutonium processed. The indirect cost considered was personnel exposure from these operations. Whole body exposures ranged from 0.04 man-rem per 100 kg of low-exposure plutonium reconstituted to 0.9 man-rem per 100 kg of average-exposure plutonium pelletized. Hand exposures were much higher - 17 man-rem power 100 kg of low-exposure plutonium reconstituted to 67 man-rem per 100 kg of average plutonium pelletized. The principal benefit is a potential twentyfold reduction of airborne release in the event of an accident. An experimental plan is outlined to fill the data gaps uncovered during this study in the areas of pelletizing and reconstitution process parameters and pellet response behavior to accident-generated stresses. A study to enhance the containment potential of the inner packaging used during shipment is also outlined

Amarillo National Resource Center for Plutonium 1999 plan

Energy Technology Data Exchange (ETDEWEB)

NONE

1999-01-30

The purpose of the Amarillo National Resource Center for Plutonium is to serve the Texas Panhandle, the State of Texas and the US Department of Energy by: conducting scientific and technical research; advising decision makers; and providing information on nuclear weapons materials and related environment, safety, health, and nonproliferation issues while building academic excellence in science and technology. This paper describes the electronic resource library which provides the national archives of technical, policy, historical, and educational information on plutonium. Research projects related to the following topics are described: Environmental restoration and protection; Safety and health; Waste management; Education; Training; Instrumentation development; Materials science; Plutonium processing and handling; and Storage.

Amarillo National Resource Center for Plutonium 1999 plan

International Nuclear Information System (INIS)

1999-01-01

The purpose of the Amarillo National Resource Center for Plutonium is to serve the Texas Panhandle, the State of Texas and the US Department of Energy by: conducting scientific and technical research; advising decision makers; and providing information on nuclear weapons materials and related environment, safety, health, and nonproliferation issues while building academic excellence in science and technology. This paper describes the electronic resource library which provides the national archives of technical, policy, historical, and educational information on plutonium. Research projects related to the following topics are described: Environmental restoration and protection; Safety and health; Waste management; Education; Training; Instrumentation development; Materials science; Plutonium processing and handling; and Storage

Plutonium Finishing Plant

Data.gov (United States)

Federal Laboratory Consortium — The Plutonium Finishing Plant, also known as PFP, represented the end of the line (the final procedure) associated with plutonium production at Hanford.PFP was also...

Implementing waste minimization at an active plutonium processing facility: Successes and progress at technical area (TA) -55 of the Los Alamos National Laboratory

Energy Technology Data Exchange (ETDEWEB)

Balkey, J.J.; Robinson, M.A.; Boak, J.

1997-12-01

The Los Alamos National Laboratory has ongoing national security missions that necessitate increased plutonium processing. The bulk of this activity occurs at Technical Area -55 (TA-55), the nations only operable plutonium facility. TA-55 has developed and demonstrated a number of technologies that significantly minimize waste generation in plutonium processing (supercritical CO{sub 2}, Mg(OH){sub 2} precipitation, supercritical H{sub 2}O oxidation, WAND), disposition of excess fissile materials (hydride-dehydride, electrolytic decontamination), disposition of historical waste inventories (salt distillation), and Decontamination & Decommissioning (D&D) of closed nuclear facilities (electrolytic decontamination). Furthermore, TA-55 is in the process of developing additional waste minimization technologies (molten salt oxidation, nitric acid recycle, americium extraction) that will significantly reduce ongoing waste generation rates and allow volume reduction of existing waste streams. Cost savings from reduction in waste volumes to be managed and disposed far exceed development and deployment costs in every case. Waste minimization is also important because it reduces occupational exposure to ionizing radiation, risks of transportation accidents, and transfer of burdens from current nuclear operations to future generations.

Implementing waste minimization at an active plutonium processing facility: Successes and progress at technical area (TA) -55 of the Los Alamos National Laboratory

International Nuclear Information System (INIS)

Balkey, J.J.; Robinson, M.A.; Boak, J.

1997-01-01

The Los Alamos National Laboratory has ongoing national security missions that necessitate increased plutonium processing. The bulk of this activity occurs at Technical Area -55 (TA-55), the nations only operable plutonium facility. TA-55 has developed and demonstrated a number of technologies that significantly minimize waste generation in plutonium processing (supercritical CO 2 , Mg(OH) 2 precipitation, supercritical H 2 O oxidation, WAND), disposition of excess fissile materials (hydride-dehydride, electrolytic decontamination), disposition of historical waste inventories (salt distillation), and Decontamination ampersand Decommissioning (D ampersand D) of closed nuclear facilities (electrolytic decontamination). Furthermore, TA-55 is in the process of developing additional waste minimization technologies (molten salt oxidation, nitric acid recycle, americium extraction) that will significantly reduce ongoing waste generation rates and allow volume reduction of existing waste streams. Cost savings from reduction in waste volumes to be managed and disposed far exceed development and deployment costs in every case. Waste minimization is also important because it reduces occupational exposure to ionizing radiation, risks of transportation accidents, and transfer of burdens from current nuclear operations to future generations

Double shell tanks plutonium inventory assessment

International Nuclear Information System (INIS)

Tusler, L.A.

1995-01-01

This report provides an evaluation that establishes plutonium inventory estimates for all DSTs based on known tank history information, the DST plutonium inventory tracking system, tank characterization measurements, tank transfer records, and estimated average concentration values for the various types of waste. These estimates use data through December 31, 1994, and give plutonium estimates as of January 1, 1995. The plutonium inventory values for the DSTs are given in Section 31. The plutonium inventory estimate is 224 kg for the DSTs and 854 kg for the SSTs for a total of 1078 kg. This value compares favorably with the total plutonium inventory value of 981 kg obtained from the total plutonium production minus plutonium recovery analysis estimates

Monitoring and detection of plutonium movement in storage vaults

International Nuclear Information System (INIS)

Kuckertz, T.H.; Bieri, J.M.; Caldwell, J.T.; France, S.W.; Hastings, R.D.; Pratt, J.C.; Shunk, E.R.; Goin, R.W.

1981-01-01

We investigated a method for monitoring a typical large storage vault for unauthorized removal of plutonium. The method is based on the assumption that the neutron field in a vault produced by a particular geometric configuration of bulk plutonium remains constant in time and space as long as the configuration is undisturbed. To observe such a neutron field, we installed an array of 25 3 He proportional counters in the ceiling of a plutonium storage vault at Argonne National Laboratory West. Data collected by each counter were processed to determine whether statistically significant changes had occurred in the neutron field. Continuous observation experiments measured the long-term stability of the system. Removal experiments were performed in which known quantities of plutonium were removed from the vault. Both types of experiments demonstrated that the neutron monitoring system can detect removal or addition of bulk plutonium (11% 240 Pu) whose mass is as small as 0.04% of the total inventory

Aqueous methods for recovery of plutonium from pyrochemical residues

International Nuclear Information System (INIS)

Muscatello, A.C.; Killion, M.E.; Fisher, D.C.

1987-01-01

Studies of the recovery of plutonium from the pyrochemical residue salts from the Direct Oxide Reduction (DOR) and Electrorefining (ER) processes have shown that chloride anion exchange is useful and effective. Our previous studies have defined the operating limits for obtaining low level effluent plutonium losses on the order of 10 -3 g/l. The knowledge obtained in work on DOR salt was extended to ER salt and a process has been demonstrated to be feasible on a larger scale. Studies of oxalate precipitation of plutonium (III) from the eluat exhibit the expected losses to the filtrate as a function of the acidity. Two alternatives to chloride anion exchange, caustic leaching and direct oxalate precipitation are also shown to be feasible for the recovery of plutonium from ER salts. The results of studies of coprocessing DOR and ER residue salts to increase ER salt throughput and decrease HC1 requirements are also presented. The feasibility of coprocessing other pyrochemical residues, such as black salts, anode heel, and ER scrapeout will be discussed

Determination of plutonium in environment

International Nuclear Information System (INIS)

Sakanoue, Masanobu

1978-01-01

Past and present methods of determining the amount of plutonium in the environment are summarized. Determination of the amount of plutonium in uranium ore began in 1941. Plutonium present in polluted environments due to nuclear explosions, nuclear power stations, etc. was measured in soil and sand in Nagasaki in 1951 and in ash in Bikini in 1954. Analytical methods of measuring the least amount of plutonium in the environment were developed twenty years later. Many studies on and reviews of these methods have been reported all over the world, and a standard analytical procedure has been adopted. A basic analytical method of measurement was drafted in Japan in 1976. The yield, treatment of samples, dissolution, separation, control of measurable ray sources determination by α spectrometry, cross-check determination, and treatment of samples containing hardly soluble plutonium were examined. At present, the amount of plutonium can be determined by all of these methods. The presence of plutonium was studied further, and the usefulness of determination of the plutonium isotope ratio is discussed. (Kumagai, S.)

Multi-generational stewardship of plutonium

International Nuclear Information System (INIS)

Pillay, K.K.S.

1997-01-01

The post-cold war era has greatly enhanced the interest in the long-term stewardship of plutonium. The management of excess plutonium from proposed nuclear weapons dismantlement has been the subject of numerous intellectual discussions during the past several years. In this context, issues relevant to long-term management of all plutonium as a valuable energy resource are also being examined. While there are differing views about the future role of plutonium in the economy, there is a recognition of the environmental and health related problems and proliferation potentials of weapons-grade plutonium. The long-term management of plutonium as an energy resource will require a new strategy to maintain stewardship for many generations to come

Decontamination of plutonium-contaminated surfaces; Essais de decontamination des surfaces contaminees par du plutonium

Energy Technology Data Exchange (ETDEWEB)

Bertrand, J; Clouet d' Orval, Ch; Tachon, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1958-07-01

The measure of the neutron distribution in the core of 'Proserpine', by means of activation detectors, requires no contact between the plutonium sulfate solution and the detectors. These detectors are put into PVC or polyethylene bags. This report describes the process used to decontaminate these bags. A washing by nitric acid followed by coating with plexiglass is kept, with this process we have no contamination on the detectors. (author) [French] La mesure de la distribution de neutrons par detecteurs a activation dans le coeur de Proserpine exige de proteger ces detecteurs contre tout contact avec la solution de plutonium. Les detecteurs sont places dans des gaines en polyvinyle ou en polyethylene. Ce rapport decrit le procede utilise pour decontaminer ces gaines. On a retenu un lavage a l'acide nitrique suivi du revetement d'une meme couche de plexiglass, ce qui permet d'eviter la contamination des detecteurs. (auteur)

Chromium in aqueous nitrate plutonium process streams: Corrosion of 316 stainless steel and chromium speciation

International Nuclear Information System (INIS)

Smith, W.H.; Purdy, G.

1994-01-01

According to the measurements made in this study, the only situation in which chromium (+6) could exist in a plutonium process solution is one in which a feed containing chromium is dissolved in a glass pot dissolver in high nitric acid concentration and at high temperature. But when the resulting feed is prepared for ion exchange, the chemical treatment reduces chromium to the +3 state. Any solution being processed through the evaporator will only contain chromium in the +3 state and any chromium salts remaining in the evaporator bottoms will be chromium +3 salts

Plutonium in the marine environment

International Nuclear Information System (INIS)

Jarvis, N.V.; Linder, P.W.; Wade, P.W.

1994-01-01

The shipping of plutonium from Europe to Japan around the Cape is a contentious issue which has raised public concern that South Africa may be at risk to plutonium exposure should an accident occur. The paper describes the containers in which the plutonium (in the form of plutonium oxide, PuO 2 ) is housed and consequences of the unlikely event of these becoming ruptured. Wind-borne pollution is considered not to be a likely scenario, with the plutonium oxide particles more likely to remain practically insoluble and sediment. Plutonium aqueous and environmental chemistry is briefly discussed. Some computer modelling whereby plutonium oxide is brought into contact with seawater has been performed and the results are presented. The impact on marine organisms is discussed in terms of studies performed at marine dump sites and after the crash of a bomber carrying nuclear warheads in Thule, Greenland in 1968. Various pathways from the sea to land are considered in the light of studies done at Sellafield, a reprocessing plant in the United Kingdom. Some recent debates in the popular scientific press, such as that on the leukemia cluster at Sellafield, are described. Plutonium biochemistry and toxicity are discussed as well as medical histories of workers exposed to plutonium. 35 refs., 2 tabs., 1 fig

Reduction of uranium and plutonium oxides by aluminum. Application to the recycling of plutonium

International Nuclear Information System (INIS)

Gallay, J.

1968-01-01

A process for treating plutonium oxide calcined at high temperatures (1000 to 2000 deg. C) with a view to recovering the metal consists in the reduction of this oxide dissolved in a mixture of aluminium, sodium and calcium fluorides by aluminium at about 1180 deg. C. The first part of the report presents the results of reduction tests carried out on the uranium oxides UO 2 and U 3 O 8 ; these are in agreement with the thermodynamic calculations of the exchange reaction at equilibrium. The second part describes the application of this method to plutonium oxides. The Pu-Al alloy obtained (60 per cent Pu) is then recycled in an aqueous medium. (author) [fr

Recommended plutonium release fractions from postulated fires. Final report

International Nuclear Information System (INIS)

Kogan, V.; Schumacher, P.M.

1993-12-01

This report was written at the request of EG ampersand G Rocky Flats, Inc. in support of joint emergency planning for the Rocky Flats Plant (RFP) by EG ampersand G and the State of Colorado. The intent of the report is to provide the State of Colorado with an independent assessment of any respirable plutonium releases that might occur in the event of a severe fire at the plant. Fire releases of plutonium are of interest because they have been used by EG ampersand G to determine the RFP emergency planning zones. These zones are based on the maximum credible accident (MCA) described in the RFP Final Environmental Impact Statement (FEIS) of 1980, that MCA is assumed to be a large airplane crashing into a RFP plutonium building.The objective of this report was first, to perform a worldwide literature review of relevant release experiments from 1960 to the present and to summarize those findings, and second, to provide recommendations for application of the experimental data to fire release analyses at Rocky Flats. The latter step requires translation between experimental and expected RFP accident parameters, or ''scaling.'' The parameters of particular concern are: quantities of material, environmental parameters such as the intensity of a fire, and the physico-chemical forms of the plutonium. The latter include plutonium metal, bulk plutonium oxide powder, combustible and noncombustible wastes contaminated with plutonium oxide powder, and residues from plutonium extraction processes

Plutonium Training Opportunities

Energy Technology Data Exchange (ETDEWEB)

Balatsky, Galya Ivanovna [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Wolkov, Benjamin [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

2015-03-26

This report was created to examine the current state of plutonium training in the United States and to discover ways in which to ensure that the next generation of plutonium workers are fully qualified.

Plutonium in the aquatic environment around the Rocky Flats facility

International Nuclear Information System (INIS)

Thompson, M.A.

1975-01-01

The Rocky Flats Plant of the United States Energy Research and Development Administration has been fabricating and chemically recovering plutonium for over 20 years. During that time, small amounts of plutonium have been released with liquid process and sanitary waste discharges. The liquid waste flows through a series of holding ponds from which it is discharged into a creek that is part of a municipal drinking water supply. The water flows for about 1.5 km between the last holding pond and the municipal drinking water reservoir. In addition, liquid wastes containing high levels of chemical contaminants and plutonium concentrations less than allowable drinking water standards have been discharged to large evaporation ponds. The fate of the plutonium in both the surface and subsurface aquatic environment has been extensively monitored and studied. It has been found that plutonium does not move very far or very rapidly through subsurface water. The majority of the plutonium released through surface water has been contained in the sediments of the plant holding ponds. Small amounts of plutonium have also been found in the sediments of the draining creek and in the sediments of the receiving reservoir. Higher than normal amounts of plutonium were released from the waste treatment plants during times when suspended solids were high. Various biological species have been examined and plutonium concentration factors determined. Considerably less than 1% of the 210 mCi of plutonium released has been detected in biological systems including man. After more than 20 years of large scale operations, no health or environmental hazard has been identified due to the release of small amounts of plutonium. (author)

Molecular Interactions of Plutonium(VI) with Synthetic Manganese-Substituted Goethite

Energy Technology Data Exchange (ETDEWEB)

Hu, Yung-Jin; Schwaiger, Luna Kestrel; Booth, Corwin H.; Kukkadapu, Ravi K.; Cristiano, Elena; Kaplan, Daniel; Nitsche, Heino

2010-03-09

Plutonium(VI) sorption on the surface of well-characterized synthetic manganese-substituted goethite minerals (Fe1-xMnxOOH) was studied using X-ray absorption spectroscopy. We chose to study the influence of manganese as a minor component in goethite, because goethite rarely exists as a pure phase in nature. Manganese X-ray absorption near-edge structure measurements indicated that essentially all the Mn in the goethite existed as Mn(III), even though Mn was added during mineral synthesis as Mn(II). Importantly, energy dispersive X-ray analysis demonstrated that Mn did not exist as discrete phases and that it was homogeneously mixed into the goethite to within the limit of detection of the method. Furthermore, Mössbauer spectra demonstrated that all Fe existed as Fe(III), with no Fe(II) present. Plutonium(VI) sorption experiments were conducted open to air and no attempt was made to exclude carbonate. The use of X-ray absorption spectroscopy allows us to directly and unambiguously measure the oxidation state of plutonium in situ at the mineral surface. Plutonium X-ray absorption near-edge structure measurements carried out on these samples showed that Pu(VI) was reduced to Pu(IV) upon contact with the mineral. This reduction appears to be strongly correlated with mineral solution pH, coinciding with pH transitions across the point of zero charge of the mineral. Furthermore, extended X-ray absorption fine structure measurements show evidence of direct plutonium binding to the metal surface as an inner-sphere complex. This combination of extensive mineral characterization and advanced spectroscopy suggests that sorption of the plutonium onto the surface of the mineral was followed by reduction of the plutonium at the surface of the mineral to form an inner-sphere complex. Because manganese is often found in the environment as a minor component associated with major mineral components, such as goethite, understanding the molecular-level interactions of plutonium with

Optimizing Plutonium stock management

International Nuclear Information System (INIS)

Niquil, Y.; Guillot, J.

1997-01-01

Plutonium from spent fuel reprocessing is reused in new MOX assemblies. Since plutonium isotopic composition deteriorates with time, it is necessary to optimize plutonium stock management over a long period, to guarantee safe procurement, and contribute to a nuclear fuel cycle policy at the lowest cost. This optimization is provided by the prototype software POMAR

Experimental and Numerical Investigations on Colloid-facilitated Plutonium Reactive Transport in Fractured Tuffaceous Rocks

Science.gov (United States)

Dai, Z.; Wolfsberg, A. V.; Zhu, L.; Reimus, P. W.

2017-12-01

Colloids have the potential to enhance mobility of strongly sorbing radionuclide contaminants in fractured rocks at underground nuclear test sites. This study presents an experimental and numerical investigation of colloid-facilitated plutonium reactive transport in fractured porous media for identifying plutonium sorption/filtration processes. The transport parameters for dispersion, diffusion, sorption, and filtration are estimated with inverse modeling for minimizing the least squares objective function of multicomponent concentration data from multiple transport experiments with the Shuffled Complex Evolution Metropolis (SCEM). Capitalizing on an unplanned experimental artifact that led to colloid formation and migration, we adopt a stepwise strategy to first interpret the data from each experiment separately and then to incorporate multiple experiments simultaneously to identify a suite of plutonium-colloid transport processes. Nonequilibrium or kinetic attachment and detachment of plutonium-colloid in fractures was clearly demonstrated and captured in the inverted modeling parameters along with estimates of the source plutonium fraction that formed plutonium-colloids. The results from this study provide valuable insights for understanding the transport mechanisms and environmental impacts of plutonium in fractured formations and groundwater aquifers.

Separation of Plutonium from Irradiated Fuels and Targets

Energy Technology Data Exchange (ETDEWEB)

Gray, Leonard W. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Holliday, Kiel S. [Lawrence Livermore National Lab. (LLNL), Livermore, CA (United States); Murray, Alice [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Thompson, Major [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Thorp, Donald T. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Yarbro, Stephen [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Venetz, Theodore J. [Hanford Site, Benton County, WA (United States)

2015-09-30

Spent nuclear fuel from power production reactors contains moderate amounts of transuranium (TRU) actinides and fission products in addition to the still slightly enriched uranium. Originally, nuclear technology was developed to chemically separate and recover fissionable plutonium from irradiated nuclear fuel for military purposes. Military plutonium separations had essentially ceased by the mid-1990s. Reprocessing, however, can serve multiple purposes, and the relative importance has changed over time. In the 1960’s the vision of the introduction of plutonium-fueled fast-neutron breeder reactors drove the civilian separation of plutonium. More recently, reprocessing has been regarded as a means to facilitate the disposal of high-level nuclear waste, and thus requires development of radically different technical approaches. In the last decade or so, the principal reason for reprocessing has shifted to spent power reactor fuel being reprocessed (1) so that unused uranium and plutonium being recycled reduce the volume, gaining some 25% to 30% more energy from the original uranium in the process and thus contributing to energy security and (2) to reduce the volume and radioactivity of the waste by recovering all long-lived actinides and fission products followed by recycling them in fast reactors where they are transmuted to short-lived fission products; this reduces the volume to about 20%, reduces the long-term radioactivity level in the high-level waste, and complicates the possibility of the plutonium being diverted from civil use – thereby increasing the proliferation resistance of the fuel cycle. In general, reprocessing schemes can be divided into two large categories: aqueous/hydrometallurgical systems, and pyrochemical/pyrometallurgical systems. Worldwide processing schemes are dominated by the aqueous (hydrometallurgical) systems. This document provides a historical review of both categories of reprocessing.

Recent advances in liquid membranes and their applications in nuclear waste processing: an overview

Energy Technology Data Exchange (ETDEWEB)

Shukla, J P; Iyer, R H [Radiochemistry Division, Bhabha Atomic Research Centre, Mumbai (India)

1994-06-01

Membrane extraction, combining the processes of extraction, scrubbing and stripping in a single step, demonstrates the inherent capability of solvent extraction under non-equilibrium conditions. Permeant transport across various liquid membrane (LM) configurations, viz. bulk liquid, emulsion liquid and supported liquid membranes has great potential for applications in the nuclear field particularly in the decontamination of low and medium level radioactive wastes. Potential practical applications of such membranes have also been envisaged in the recovery of metals from hydrometallurgical leach solutions and in plutonium and americium removal from nitric acid waste streams generated by plutonium recovery operations in the PUREX process. Studies carried out have established that minor actinides like uranium, plutonium and americium from process effluents can easily be transported across polymeric and liquid type membranes through the use of specific ionophores dissolved in an appropriate liquid membrane phase. The possibility of the membrane extraction of fission palladium from acidic wastes has also been demonstrated by the use of some soft bases. An overview of these results and also some of the recent radiochemical applications of energy - efficient LM processes including directions for future research are outlined in this paper. (author). 19 refs., 1 fig., 2 tabs.

Treatment of plutonium contaminations

International Nuclear Information System (INIS)

Lafuma, J.

1983-01-01

Three kinds of plutonium contaminations were considered: skin contamination; contaminated wounds; contamination by inhalation. The treatment of these contaminations was studied for insoluble (oxide and metal forms) and soluble plutonium (complexes). The use of DTPA and therapeutic problems encountered with stable plutonium complexes were analyzed. The new possibilities of internal decontamination using Puchel and LICAM were evaluated [fr

Matrix Characterization of Plutonium Residues by Alpha-Particle Self-Interrogation

International Nuclear Information System (INIS)

Prettyman, T.H.; Foster, L.A.; Staples, P.

1998-01-01

Legacy plutonium residues often have inadequate item descriptions. Nondestructive characterization can help segregate these items for reprocessing or provide information needed for disposal or storage. Alpha particle-induced gamma-ray spectra contain a wealth of information that can be used for matrix characterization. We demonstrate how this information can be used for item identification. Gamma-ray spectra were recorded at the Los Alamos Plutonium Facility from a variety of legacy, plutonium-processing residues and product materials. The comparison and analysis of these spectra are presented

Plutonium uptake by plants from soil containing plutonium-238 dioxide particles. Final report

International Nuclear Information System (INIS)

Brown, K.W.; McFarlane, J.C.

1977-05-01

Three plant species--alfalfa, lettuce, and radishes were grown in soils contaminated with plutonium-238 dioxide (238)PuO2 at concentrations of 23, 69, 92, and 342 nanocuries per gram (nCi/g). The length of exposure varied from 60 days for the lettuce and radishes to 358 days for the alfalfa. The magnitude of plutonium incorporation as indicated by the discrimination ratios for these species, after being exposed to the relatively insoluble PuO2, was similar to previously reported data using different chemical forms of plutonium. Evidence indicates that the predominant factor in plutonium uptake by plants may involve the chelation of plutonium contained in the soils by the action of compounds such as citric acid and/or other similar chelating agents released from the plant roots

The plutonium utilization in thermal and fast reactor in Japan

International Nuclear Information System (INIS)

Amanuma, T.; Uematsu, K.

1977-01-01

The nuclear power development in Japan is rather extensive one, and the installed nuclear power capacity is expected to reach 49,000 MWe by 1985 and possibly to reach 170,000 MWe by 2000 according to a prediction. Currently istalled nuclear power is mainly based on Light Water type Reactor, and this trend is expected to persist for the time-being. The plutonium produced by LWR will be accumulated to 20 tons by 1985 and to more than 200 tons by 2000. If the produced plutonium will simply be stored, it will raise the economic pressure to utilities and the management and physical protection problems associated with plutonium storing. Therefore, it is not too wise simply to store plutonium in a locked vault. In Japan, there are three ways of solving these problems which are currently worked out. There is no doubt that the best solution is to use plutonium in fast reactors. To reach this goal, an Experimental Fast Reactor ''JOYO''has been constructed and it is waiting for criticality in very near future. A prototype fast breeder reactor ''MONJU'', which is designed for about 300 MWe, is nearing to the last stage of the design work. The start of its construction will take place in a few yesars. The domonstration fast breeder reactor will come next to ''MONJU'' and the large scale commercial use of fast breeder reactor is expected to start around 1995. To anwer the near-term need for plutonium utilization, two technologies, which are equally important to Japan, are currently developed. One is the recycle use of plutonium into LWR. This technology has long been jointly developed by research organizations and utilities. Some of fuel irradiation data are already obtained and the physics study has also been extensive. The application of this technology is expected to start about 1987. The other is to burn plutonium in an Advanced Thermal Reactor (D 2 O moderated, Boiling Water Cooled) which shows better characteristics of using plutonium. The 160 MWe ''Fugen'' is a prototype

Test plan for demonstrating plutonium extraction from 10-L solutions using EIChrom extraction chromatographic resins

International Nuclear Information System (INIS)

Barney, G.S.

1994-01-01

Corrosive plutonium solutions stored in 10-L containers at the Plutonium Finishing Plant must be treated to convert the plutonium to a safe, solid form for storage and to remove the americium so that radiation exposure can be reduced. Extraction chromatographic resins will be tested for separating plutonium from these solutions in the laboratory. Separation parameters will be developed during the testing for large scale processing of the 10-L solutions and solutions of similar composition. Use of chromatographic resins will allow plutonium separation with minimum of chemical addition to the feed and without the need for plutonium valence adjustment. The separated plutonium will be calcined to plutonium oxide by direct solution calcination

Plutonium in a grassland ecosystem

International Nuclear Information System (INIS)

Little, C.A.

1976-08-01

A study was made of plutonium contamination of grassland at the Rocky Flats plant northwest of Denver, Colorado. Of interest were: the definition of major plutonium-containing ecosystem compartments; the relative amounts in those compartments; how those values related to studies done in other geographical areas; whether or not the predominant isotopes, 238 Pu and 239 Pu, behaved differently; and what mechanisms might have allowed for the observed patterns of contamination. Samples of soil, litter, vegetation, arthropods, and small mammals were collected for Pu analysis and mass determination from each of two macroplots. Small aliquots (5 g or less) were analyzed by a rapid liquid scintillation technique and by alpha spectrometry. Of the compartments sampled, greater than 99 percent of the total plutonium was contained in the soil and the concentrations were significantly inversely correlated with distance from the contamination source, depth of the sample, and particle size of the sieved soil samples. The soil data suggested that the distribution of contamination largely resulted from physical transport processes

Recovery of americium-241 from aged plutonium metal

International Nuclear Information System (INIS)

Gray, L.W.; Burney, G.A.; Reilly, T.A.; Wilson, T.W.; McKibben, J.M.

1980-12-01

About 5 kg of ingrown 241 Am was recovered from 850 kg of aged plutonium using a process developed specifically for Savannah River Plant application. The aged plutonium metal was first dissolved in sulfamic acid. Sodium nitrite was added to oxidize the plutonium to Pu(IV) and the residual sulfamate ion was oxidized to nitrogen gas and sulfate. The plutonium and americium were separated by one cycle of solvent extraction. The recovered products were subsequently purified by cation exchange chromatography, precipitated as oxalates, and calcined to the oxides. Plutonium processng was routine. Before cation exchange purification, the aqueous americium solution from solvent extraction was concentrated and stripped of nitric acid. More than 98% of the 241 Am was then recovered from the cation exchange column where it was effectively decontaminated from all major impurities except nickel and chromium. This partially purified product solution was concentrated further by evaporation and then denitrated by reaction with formic acid. Individual batches of americium oxalate were then precipitated, filtered, washed, and calcined. About 98.5% of the americium was recovered. The final product purity averaged 98% 241 AmO 2 ; residual impurities were primarily lead and nickel

Plutonium isotopes in the environment

International Nuclear Information System (INIS)

Holm, E.

1977-12-01

Determination of plutonium and americium by ion exchange and alpha-spectrometry. Deposition of global fall-out and accumulated area-content of 238 Pu, 239 Pu, 240 Pu, 241 Pu, 242 Pu and 241 Am in central Sweden (62.3 deg N, 12.4 deg E), by using the lichen species Cladonia alpestris as bioindicator. Retention and distribution of plutonium in carpets of lichen and soil. Transfer of plutonium from lichen to reindeer and man. Absorbed dose in reindeer and man from plutonium. Basic studies of plutonium and americium in the western Mediterranean surface waters, with emphases on particulate form of the transuranics. (author)

High-temperature vacuum distillation separation of plutonium waste salts

International Nuclear Information System (INIS)

Garcia, E.

1996-01-01

In this task, high-temperature vacuum distillation separation is being developed for residue sodium chloride-potassium chloride salts resulting from past pyrochemical processing of plutonium. This process has the potential of providing clean separation of the salt and the actinides with minimal amounts of secondary waste generation. The process could produce chloride salt that could be discarded as low-level waste (LLW) or low actinide content transuranic (TRU) waste, and a concentrated actinide oxide powder that would meet long-term storage standards (DOE-DTD-3013-94) until a final disposition option for all surplus plutonium is chosen

The first metallurgical tests on plutonium; Premiers essais metallurgiques sur le plutonium

Energy Technology Data Exchange (ETDEWEB)

Grison, E; Abramson, R; Anselin, F; Monti, H [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1958-07-01

Metallic plutonium was first prepared in France in January 1956, as soon as we had access to quantities of the order of several grams of plutonium, which had been extracted from the rods of the pile EL2 at Saclay. Since up to the present this reactor, of thermal power 2 000 kW, has been our only source of plutonium, we have so far only worked on experimental quantities sufficient for the basic tests but not for tests on a scale of possible applications. It is this work, carried out during this phase of preliminary research, which is described below. With the starting up of the plutonium extraction plant at Marcoule, where the reactor G1 has been operating at power for more than a year, we shall go on next to a another order of magnitude which will allow the manufacture and experimentation of prototype fuel elements. (author) [French] La premiere elaboration de plutonium metallique en France fut faite en janvier 1956, des que nous pumes disposer de quantites de plutonium de l'ordre de quelques grammes, qui avaient ete retires des barreaux de la pile EL2 de Saclay. Ce reacteur, d'une puissance thermique de 2 000 kW, ayant ete jusqu'a present notre seule source de plutonium, nous n'avons encore travaille que sur des quantites experimentales suffisantes pour les essais de base, mais non pour des essais a l'echelle d'applications possibles. Ce sont les travaux effectues pendant cette phase de recherches preliminaires qui seront evoques ci-dessous. Avec la mise eu route de l'usine d'extraction de plutonium de Marcoule, ou le reacteur G1 fonctionne en puissance depuis plus d'un an, nous allons passer prochainement a un autre ordre de grandeur, qui nous permettra la fabrication et l'experimentation d'elements combustibles prototypes. (auteur)

Plutonium oxides and uranium and plutonium mixed oxides. Carbon determination

International Nuclear Information System (INIS)

Anon.

Determination of carbon in plutonium oxides and uranium plutonium mixed oxides, suitable for a carbon content between 20 to 3000 ppm. The sample is roasted in oxygen at 1200 0 C, the carbon dioxide produced by combustion is neutralized by barium hydroxide generated automatically by coulometry [fr

Progress report for 1982/83 from the Plutonium Contaminated Materials Working Party

International Nuclear Information System (INIS)

Higson, S.G.

1983-01-01

The report falls under the headings: introduction (definitions of plutonium contaminated materials (PCM)); organisation and role of the Plutonium Contaminated Materials Working Party; management practices in relation to PCM; 1982/1983 Progress Report (engineering objectives; reduction of PCM arisings; plutonium measurement; development of treatment processes; decommissioning and non-combustible PCM treatment; washing of shredded combustible PCM; PCM immobilisation; liquid effluent treatment; actinide chemistry); programme management. (U.K.)

Treatment of plutonium contamined solid wastes by electrogenerated Ag(II)

International Nuclear Information System (INIS)

Saulze, J.L.

1990-01-01

A process for the treatment of plutonium contaminated solid wastes is designed. Two types of wastes have been studied; incineration ashes (COGEMA UP1) and sludges produced in the cryotreatment facility in Cadarache Center (France). The principle of the process is based on the rapid dissolution of PuO 2 (contained in the wastes) under the action of aggressive Ag(II) species, regenerated electrochemically. In the case of the treatment of incinerator ashes an electrochemical pretreatment is necessary if the chloride ion content of the ashes is high. The feasibility of the decontamination process has been proved for the two types of plutonium contaminated solid wastes at a pilot level; for example 1 Kg of ashes (or 0.75 Kg of sludges) has been treated in one experiment, and 97% (or 95%) of the total plutonium was dissolved at the end of the experiment. Industrial applications of this new process are underway [fr

Plutonium Immobilization Program cold pour tests

International Nuclear Information System (INIS)

Hovis, G.L.; Stokes, M.W.; Smith, M.E.; Wong, J.W.

1999-01-01

The Plutonium Immobilization Program (PIP) is a joint venture between the Savannah River Site, Lawrence Livermore National Laboratory, Argonne National Laboratory, and Pacific Northwest National Laboratory to carry out the disposition of excess weapons-grade plutonium. This program uses the can-in-canister (CIC) approach. CIC involves encapsulating plutonium in ceramic forms (or pucks), placing the pucks in sealed stainless steel cans, placing the cans in long cylindrical magazines, latching the magazines to racks inside Defense Waste Processing Facility (DWPF) canisters, and filling the DWPF canisters with high-level waste glass. This process puts the plutonium in a stable form and makes it attractive for reuse. At present, the DWPF pours glass into empty canisters. In the CIC approach, the addition of a stainless steel rack, magazines, cans, and ceramic pucks to the canisters introduces a new set of design and operational challenges: All of the hardware installed in the canisters must maintain structural integrity at elevated (molten-glass) temperatures. This suggests that a robust design is needed. However, the amount of material added to the DWPF canister must be minimized to prevent premature glass cooling and excessive voiding caused by a large internal thermal mass. High metal temperatures, minimizing thermal mass, and glass flow paths are examples of the types of technical considerations of the equipment design process. To determine the effectiveness of the design in terms of structural integrity and glass-flow characteristics, full-scale testing will be conducted. A cold (nonradioactive) pour test program is planned to assist in the development and verification of a baseline design for the immobilization canister to be used in the PIP process. The baseline design resulting from the cold pour test program and CIC equipment development program will provide input to Title 1 design for second-stage immobilization. The cold pour tests will be conducted in two

The first milligrams of plutonium

International Nuclear Information System (INIS)

Goldschmidt, B.

1997-01-01

A historical review of the development of the very first quantities of plutonium produced during World War II in the United States and in Canada, as remembered by the French nuclear chemist, Mr Goldschmidt, who participated to the various programs which were involved in the development of the atomic bomb, and to the first steps of the French atomic program after the war. Mr Goldschmidt worked especially on organic solvent extraction, with the selection, in 1945, of non volatile tri glycol dichloride, and the development of the Chalk River plant. In 1949, at the Bouchet plant, his team has isolated the first milligrams of French plutonium from uranium oxide; and in 1952, the PUREX process was developed

Plutonium Immobilization Can Loading Concepts

International Nuclear Information System (INIS)

Kriikku, E.; Ward, C.; Stokes, M.; Randall, B.; Steed, J.; Jones, R.; Hamilton, L.; Rogers, L.; Fiscus, J.; Dyches, G.

1998-05-01

The Plutonium Immobilization Facility will encapsulate plutonium in ceramic pucks and seal the pucks inside welded cans. Remote equipment will place these cans in magazines and the magazines in a Defense Waste Processing Facility (DWPF) canister. The DWPF will fill the canister with glass for permanent storage. This report discusses five can loading conceptual designs and the lists the advantages and disadvantages for each concept. This report identifies loading pucks into cans and backfilling cans with helium as the top priority can loading development areas. The can loading welder and cutter are very similar to the existing Savannah River Site (SRS) FB-Line bagless transfer welder and cutter and thus they are a low priority development item

The role of troublesome components in plutonium vitrification

Energy Technology Data Exchange (ETDEWEB)

Li, Hong; Vienna, J.D.; Peeler, D.K.; Hrma, P.; Schweiger, M.J. [Pacific Northwest National Lab., Richland, WA (United States)

1996-05-01

One option for immobilizing surplus plutonium is vitrification in a borosilicate glass. Two advantages of the glass form are (1) high tolerance to feed variability and, (2) high solubility of some impurity components. The types of plutonium-containing materials in the United States inventory include: pits, metals, oxides, residues, scrap, compounds, and fuel. Many of them also contain high concentrations of carbon, chloride, fluoride, phosphate, sulfate, and chromium oxide. To vitrify plutonium-containing scrap and residues, it is critical to understand the impact of each component on glass processing and chemical durability of the final product. This paper addresses glass processing issues associated with these troublesome components. It covers solubility limits of chlorine, fluorine, phosphate, sulfate, and chromium oxide in several borosilicate based glasses, and the effect of each component on vitrification (volatility, phase segregation, crystallization, and melt viscosity). Techniques (formulation, pretreatment, removal, and/or dilution) to mitigate the effect of these troublesome components are suggested.

Cigarette smoke and plutonium

International Nuclear Information System (INIS)

Filipy, R.E.

1985-01-01

Autoradiographic techniques with liquid photographic emulsion and cellulose nitrate track-etch film are being used to investigate the spatial distribution of inhaled plutonium in the lungs of beagle dogs exposed to cigarette smoke or to the plutonium aerosol only. More plutonium than expected was detected on the inner surfaces of bronchi, and particles were observed beneath the bronchial mucosa. 2 figures, 2 tables

Recovery of plutonium from electrorefining anode heels at Savannah River

International Nuclear Information System (INIS)

Gray, J.H.; Gray, L.W.; Karraker, D.G.

1987-03-01

In a joint effort, the Savannah River Laboratory (SRL), Savannah River Plant (SRP), and the Rocky Flats Plant (RFP) have developed two processes to recover plutonium from electrorefining anode heel residues. Aqueous dissolution of anode heel metal was demonstrated at SRL on a laboratory scale and on a larger pilot scale using either sulfamic acid or nitric acid-hydrazine-fluoride solutions. This direct anode heel metal dissolution requires the use of a geometrically favorable dissolver. The second process developed involves first diluting the plutonium in the anode heel residues by alloying with aluminum. The alloyed anode heel plutonium can then be dissolved using a nitric acid-fluoride-mercury(II) solution in large non-geometrically favorable equipment where nuclear safety is ensured by concentration control

Process for plutonium rextraction in aqueous solution from an organic solvent, especially for uranium plutonium partition

International Nuclear Information System (INIS)

Germain, M.; Gillet, B.; Pasquiou, J.Y.

1989-01-01

The organic solvent containing plutonium is contacted with an aqueous solution of a uranous salt, for instance uranous nitrate, and a hydroxylamine salt, for instance the nitrate. In these conditions uranous nitrate is a reducing agent of Pu III and hydroxylamine nitrate stabilizes Pu III and U IV in the aqueous phase. Performances are similar to these of the U IV-hydrazine nitrate without interference of hydrazine nitrate degradation products [fr

A performance indicator for reduction in vulnerability through stabilization of plutonium

International Nuclear Information System (INIS)

Marchese, A.R.; Neogy, P.; Azarm, M.A.

1997-01-01

The US Department of Energy (DOE) is currently storing several metric tons of plutonium in various forms in a variety of facilities throughout the DOE complex. Since the cessation of weapons production in 1990, many of these facilities with plutonium in storage have not operated. Since the shutdown was regarded as temporary, little attempt was made at that time to empty the process lines of plutonium, or to place the plutonium in containers or packages that would provide safe storage for extended periods of time. As a result, the packages and containers providing interim storage are vulnerable to failure through leakage, rupture and other modes, and pose potential hazards to facility workers, the public and the environment. Here, an approach to measuring and tracking the reduction in vulnerabilities resulting from stabilizing and repackaging plutonium is developed and presented. The approach utilizes results obtained by the DOE Working Group on the vulnerabilities associated with plutonium storage

HB-Line Plutonium Oxide Data Collection Strategy

Energy Technology Data Exchange (ETDEWEB)

Watkins, R. [Savannah River Nuclear Solutions; Varble, J. [Savannah River Nuclear Solutions; Jordan, J. [Savannah River Nuclear Solutions

2015-05-26

HB-Line and H-Canyon will handle and process plutonium material to produce plutonium oxide for feed to the Mixed Oxide Fuel Fabrication Facility (MFFF). However, the plutonium oxide product will not be transferred to the MFFF directly from HB-Line until it is packaged into a qualified DOE-STD-3013-2012 container. In the interim, HB-Line will load plutonium oxide into an inner, filtered can. The inner can will be placed in a filtered bag, which will be loaded into a filtered outer can. The outer can will be loaded into a certified 9975 with getter assembly in compliance with onsite transportation requirement, for subsequent storage and transfer to the K-Area Complex (KAC). After DOE-STD-3013-2012 container packaging capabilities are established, the product will be returned to HB-Line to be packaged into a qualified DOE-STD-3013-2012 container. To support the transfer of plutonium oxide to KAC and then eventually to MFFF, various material and packaging data will have to be collected and retained. In addition, data from initial HB-Line processing operations will be needed to support future DOE-STD-3013-2012 qualification as amended by the HB-Line DOE Standard equivalency. As production increases, the volume of data to collect will increase. The HB-Line data collected will be in the form of paper copies and electronic media. Paper copy data will, at a minimum, consist of facility procedures, nonconformance reports (NCRs), and DCS print outs. Electronic data will be in the form of Adobe portable document formats (PDFs). Collecting all the required data for each plutonium oxide can will be no small effort for HB-Line, and will become more challenging once the maximum annual oxide production throughput is achieved due to the sheer volume of data to be collected. The majority of the data collected will be in the form of facility procedures, DCS print outs, and laboratory results. To facilitate complete collection of this data, a traveler form will be developed which

Airborne plutonium transported during southwesterly winds near the Hanford Prosser Barricade

International Nuclear Information System (INIS)

Sehmel, G.A.

1980-01-01

Airborne plutonium could result from resuspension of nuclear-weapons-testing stratospheric fallout deposition. To determine this possible resuspension at the Hanford site, two field experiments between April 12 to june 29, 1976 and August 12, 1976 to January 11, 1977 were conducted near the Prosser Barricade in the Hanford area about 19 to 22 km southeast (140 0 to 160 0 ) of the fuel-processing areas. The primary objective of these experimentss was to determine if stratospheric fallout resuspension was reflected by airborne plutonium concentrations increasing with increasing wind speed. A secondary objective was to confirm the source of the airborne plutonium by determining the plutonium-240 isotopic content or the plutonium-240/plutonium-239-mass ratio. Stratospheric fallout can be identified by the ratio of 240 Pu to other plutonium isotopes in surface soils. Plutonium was transported during southwesterly winds during the two study periods at the Prosser Barricade. Airborne 239 240 Pu concentrations varied as powers of wind speed (U):U -0 2 to U 7 8 . The airborne solids content ranged from 6 x 10 -8 to 1.7 x 10 -6 μCi/g. The 240 Pu isotopic content ranged from 5.6 to 8.1 atom percent and the 240 Pu/ 239 Pu mass ratio ranged from 0.065 to 0.089. The estimated fraction of stratospheric fallout plutonium in these samples was less than 0.24. The remaining airborne plutonium was probably of Hanford origin. Airborne plutonium probably represents resuspension of plutonium from undetermined sites by mechanisms and events not clear at present. An increasing airborne plutonium concentration with increasing wind speed might be expected for an upwind resuspension source(s). However, the geographical source(s) location was not investigated in this study

Plutonium Immobilization Project Binder Burnout and Sintering Studies (Milestone 6.6a)

International Nuclear Information System (INIS)

Chandler, G.

1999-01-01

The Plutonium Immobilization Team has developed an integrated test program to understand and optimize the controlling variables for the sintering step of the plutonium immobilization process. Sintering is the key process step that controls the product mineralogy. It is expected that the sintering will be the limiting process step that controls the throughput of the production line. The goal of the current sintering test program is to better understand factors that affect the sintering process

Plutonium Immobilization Project Binder Burnout and Sintering Studies (Milestone 6.6a)

Energy Technology Data Exchange (ETDEWEB)

Chandler, G.

1999-10-28

The Plutonium Immobilization Team has developed an integrated test program to understand and optimize the controlling variables for the sintering step of the plutonium immobilization process. Sintering is the key process step that controls the product minerology. It is expected that the sintering will be the limiting process step that controls the throughput of the production line. The goal of the current sintering test program is to better understand factors that affect the sintering process.

Chinese strategic weapons and the plutonium option (U)

Energy Technology Data Exchange (ETDEWEB)

Lewis, John W.; Xui Litai

1988-04-01

In their article "Chinese Strategic Weapons and the Plutonium Option," John W. Lewis and Xue Litai of the Center for International Security and Arms Control at Stanford University's International Strategic Institute present an unclassified look at plutonium processing in the PRC. The article draws heavily on unclassified PRC sources for its short look at this important subject. Interested readers will find more detailed information in the recently available works referenced in the article.

Safety problems relating to plutonium recycling in light water reactors

International Nuclear Information System (INIS)

Devillers, C.; Frison, J.M.; Mercier, J.P.; Revais, J.P.

1991-01-01

This paper describes the specific nature, as regards safety, of the mixed oxide (MOX) fuel cycle, with the exception of safety problems relating to the operation of nuclear power plants. These specific characteristics are due mainly to the presence of plutonium in fresh fuel and to the higher plutonium and transuranic element content in spent fuel assemblies. The fuel cycle steps analysed here are the transport of plutonium oxide, the manufacture of MOX fuel assemblies, the transport of fresh and spent fuel assemblies and the processing of spent fuel assemblies

Safety problems relating to plutonium recycling in light water reactors

International Nuclear Information System (INIS)

Devillers, C.; Frison, J.M.; Mercier, J.P.; Revais, J.P

1991-01-01

This paper describes the specific nature, as regards safety, of the mixed oxide (MOX) fuel cycle, with the exception of safety problems relating to the operation of nuclear power plants. These specific characteristics are due mainly to the presence of plutonium in fresh fuel and to the higher plutonium and transuranic element content in spent fuel assemblies. The fuel cycle steps analysed here are the transport of plutonium oxide, the manufacture of MOX fuel assemblies, the transport of fresh and spent fuel assemblies and the processing of spent fuel assemblies. (author) [fr

The problem of utilization of the military uranium and plutonium

International Nuclear Information System (INIS)

Feoktistov, L.P.

1995-01-01

The problem on military uranium and plutonium is considered from the viewpoint of their utilization as a source of fissionable materials for NPPs. The solution consists in combining spherical geometry of critical mass with enriched center and the uranium burnup expansion recess. It is necessary thereby to obtain the minimum plutonium consumption in order to draw in unlimited quaintness of uranium-238 in the burnup process. It is estimated that hundred reactors with the total capacity of several hundred gigawatt may be involved into operation with the help of military plutonium. Refs. 2

Coordinated safeguards for materials management in a uranium--plutonium nitrate-to-oxide coconversion facility: Coprecal

International Nuclear Information System (INIS)

Dayem, H.A.; Cobb, D.D.; Dietz, R.J.; Hakkila, E.A.; Kern, E.A.; Schelonka, E.P.; Shipley, J.P.; Smith, D.B.

1979-02-01

This report describes the conceptual design of an advanced materials-management system for safeguarding special nuclear materials in a uranium--plutonium nitrate-to-oxide coconversion facility based on the Coprecal process. Design concepts are presented for near real-time (dynamic) accountability by forming dynamic materials balances from information provided by chemical and nondestructive analyses and from process-control instrumentation. Modeling and simulation techniques are used to compare the sensitivities of proposed dynamic materials accounting strategies to both abrupt and protracted diversion. The safeguards implications of coconversion as well as some unique features of the reference process are discussed and design criteria are identified to improve the safeguardability of the Coprecal coconversion process

EIS Data Call Report: Plutonium immobilization plant using ceramic in new facilities at the Savannah River Site

International Nuclear Information System (INIS)

DiSabatino, A.

1998-01-01

The Plutonium Immobilization Plant (PIP) accepts plutonium (Pu) from pit conversion and from non-pit sources and, through a ceramic immobilization process, converts the plutonium into an immobilized form that can be disposed of in a high level waste (HLW) repository. This immobilization process is shown conceptually in Figure 1-1. The objective is to make an immobilized form, suitable for geologic disposal, in which the plutonium is as inherently unattractive and inaccessible as the plutonium in spent fuel from commercial reactors. The ceramic immobilization alternative presented in this report consists of first converting the surplus material to an oxide, followed by incorporating the plutonium oxide into a titanate-based ceramic material that is placed in metal cans

Hazards of plutonium and fuel reprocessing

International Nuclear Information System (INIS)

Watson, G.M.

1978-01-01

Apart from the possibility that civil plutonium may be diverted to military use the main argument against the introduction of a plutonium economy seems to be the supposedly unmanageable biological risk attached to plutonium itself. The author points out weaknesses in many of the opponents' arguments against the increased use of plutonium and argues that current safety practices are more than adequate in handling plutonium and other radioactive materials

Neutron monitoring of plutonium at the ZPPR storage vault

International Nuclear Information System (INIS)

Caldwell, J.T.; Kuckertz, T.H.; Bieri, J.M.; France, S.W.; Goin, R.W.; Hastings, R.D.; Pratt, J.C.; Shunk, E.R.

1981-12-01

We investigated a method for monitoring a typical large storage vault for unauthorized removal of plutonium. The method is based on the assumption that the neutron field in a vault produced by a particular geometric configuration of bulk plutonium remains constant in time and space as long as the configuration is undisturbed. To observe such a neutron field, we installed an array of 25 neutron detectors in the ceiling of a plutonium storage vault at Argonne National Laboratory West. Each neutron detector provided an independent spatial measurement of the vault neutron field. Data collected by each detector were processed to determine whether statistically significant changes had occurred in the neutron field. Continuous observation experiments measured the long-term stability of the system. Removal experiments were performed in which known quantities of plutonium were removed from the vault. Both types of experiments demonstrated that the neutron monitoring system can detect removal or addition of bulk plutonium (11% 240 Pu) whose mass is as small as 0.04% of the total inventory

Plutonium Immobilization Project - Robotic canister loading

International Nuclear Information System (INIS)

Hamilton, R.L.

2000-01-01

The Plutonium Immobilization Program (PIP) is a joint venture between the Savannah River Site (SRS), Lawrence Livermore National Laboratory (LLNL), Argonne National Laboratory (ANL), and Pacific Northwest National Laboratory (PNNL). When operational in 2008, the PIP will fulfill the nation's nonproliferation commitment by placing surplus weapons-grade plutonium in a permanently stable ceramic form and making it unattractive for reuse. Since there are significant radiation and security concerns, the program team is developing novel and unique technology to remotely perform plutonium immobilization tasks. The remote task covered in this paper employs a jointed arm robot to load seven 3.5 inch diameter, 135-pound cylinders (magazines) through the 4 inch diameter neck of a stainless steel canister. Working through the narrow canister neck, the robot secures the magazines into a specially designed rack pre-installed in the canister. To provide the deterrent effect, the canisters are filled with a mixture of high-level waste and glass at the Defense Waste Processing Facility (DWPF)

Plutonium safe handling

International Nuclear Information System (INIS)

Tvehlov, Yu.

2000-01-01

The abstract, prepared on the basis of materials of the IAEA new leadership on the plutonium safe handling and its storage (the publication no. 9 in the Safety Reports Series), aimed at presenting internationally acknowledged criteria on the radiation danger evaluation and summarizing the experience in the safe management of great quantities of plutonium, accumulated in the nuclear states, is presented. The data on the weapon-class and civil plutonium, the degree of its danger, the measures for provision of its safety, including the data on accident radiation consequences with the fission number 10 18 , are presented. The recommendations, making it possible to eliminate the super- criticality danger, as well as ignition and explosion, to maintain the tightness of the facility, aimed at excluding the radioactive contamination and the possibility of internal irradiation, to provide for the plutonium security, physical protection and to reduce irradiation are given [ru

Plans and equipment for criticality measurements on plutonium-uranium nitrate solutions

International Nuclear Information System (INIS)

Lloyd, R.C.; Clayton, E.D.; Durst, B.M.

1982-01-01

Data from critical experiments are required on the criticality of plutonium-uranium nitrate solutions to accurately establish criticality control limits for use in processing and handling of breeder type fuels. Since the fuel must be processed both safely and economically, it is necessary that criticality considerations be based on accurate experimental data. Previous experiments have been reported on plutonium-uranium solutions with Pu weight ratios extending up to some 38 wt %. No data have been presented, however, for plutonium-uranium nitrate solutions beyond this Pu weight ratio. The current research emphasis is on the procurement of criticality data for plutonium-uranium mixtures up to 60 wt % Pu that will serve as the basis for handling criticality problems subsequently encountered in the development of technology for the breeder community. Such data also will provide necessary benchmarks for data testing and analysis on integral criticality experiments for verification of the analytical techniques used in support of criticality control. Experiments are currently being performed with plutonium-uranium nitrate solutions in stainless steel cylindrical vessels and an expandable slab tank system. A schematic of the experimental systems is presented

Some of the properties of plutonium and the aluminium-plutonium alloy; Quelques proprietes du plutonium et de l'alliage aluminium-plutonium

Energy Technology Data Exchange (ETDEWEB)

Abramson, R; Boucher, R; Fabre, R; Monti, H [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1959-07-01

1- Study of the physical properties of plutonium. 1) Study of the allotropy of plutonium. a) Thermal analysis: the apparatus used and the measurement technique are briefly described. The transition point temperatures and the corresponding heats of transformation have been determined. Finally, the results of the particular study of certain transition points are given. b) Dilatometry. The dilatometric analysis of the phase changes of plutonium has been carried out by means of the Chevenard dilatometer with photographic recording. The testing conditions (heating and cooling speeds, isotherm plateaux) have been varied in order to determine accurately the characteristics of each transition, particularly the {delta} {yields} {gamma} transition on cooling. 2) Micrography of plutonium. For the accurate preparation of metallographic samples the electrolytic polishing must be rapid, which implies a mechanical polishing of excellent quality. Information is given on new attacking reagents which show the structure of the metal very clearly. 2- Study of aluminium-plutonium alloys. Comparative study of Al-Pu and Al-U alloys rich in aluminium. a) Thermal analysis. The liquids and fusion temperatures of the eutectic Al-XAl{sub 4}, have been accurately determined. From the measurement of the heats of fusion the exact composition of the eutectic alloy has been determined. b) Thermal treatments. The eutectic coalescence kinetics have been studied by a micrographic method and by following the evolution of hardness. The results obtained show that the phenomenon is more rapid in Al-Pu alloys than in Al-U alloys. c) Micrographic study of the transition XAl{sub 3} {yields} XAl{sub 4}. The peritectic reaction XAl{sub 3} + liq. {yields} XAl{sub 4} has been suppressed by quenching. The transformation of the XAl{sub 3} phase to the solid phase has been studied as well as the effect of small additions of silicon on the kinetics of this reaction. (author) [French] 1- Etude des proprietes

Salt stripping: a pyrochemical approach to the recovery of plutonium electrorefining salt residues

International Nuclear Information System (INIS)

Christensen, D.C.; Mullins, L.J.

1982-10-01

A pyrochemical process has been developed to take the salt residue from the plutonium electrorefining process and strip the plutonium from it. The process, called salt stripping, uses calcium as a reducing/coalescing agent. In a one-day operation, greater than 95% of the plutonium can be recovered as a metallic button. As much as 88% of the residue is either reused as metal or discarded as a clean salt. A thin layer of black salts, which makes up the bulk of the unrecovered Pu, is a by-product of the initial reductions. A number of black salts can be collected together and re-reduced in a second step. Greater than 88% of this plutonium can be successfully recovered in this second stage with the resulting residues being discardable. The processing time, number of processor hours, and the volume of secondary residues are greatly reduced over the classical aqueous recovery methods. In addition, the product metal is of sufficient quality to be fed directly to the electrorefining process for purification. 8 figures, 7 tables

Recovery of plutonium from incinerator ash at Rocky Flats

International Nuclear Information System (INIS)

Johnson, T.C.

1976-01-01

Incineration of combustible materials highly contaminated with plutonium produces a residue of incinerator ash. Recovery of plutonium from incinerator ash residues at Rocky Flats is accomplished by a continuous leaching operation with nitric acid containing fluoride ion. Special equipment used in the leaching operation consists of a screw feeder, air-lift dissolvers, filters, solids dryer, and vapor collection system. Each equipment item is described in detail. The average dissolution efficiency of plutonium experienced with the process was 68% on the first pass, 74% on the second pass, and 64% on each subsequent pass. Total-solids dissolution efficiencies averaged 47% on the first pass and about 25% on each subsequent pass

Burning weapons-grade plutonium in reactors

International Nuclear Information System (INIS)

Newman, D.F.

1993-06-01

As a result of massive reductions in deployed nuclear warheads, and their subsequent dismantlement, large quantities of surplus weapons- grade plutonium will be stored until its ultimate disposition is achieved in both the US and Russia. Ultimate disposition has the following minimum requirements: (1) preclude return of plutonium to the US and Russian stockpiles, (2) prevent environmental damage by precluding release of plutonium contamination, and (3) prevent proliferation by precluding plutonium diversion to sub-national groups or nonweapons states. The most efficient and effective way to dispose of surplus weapons-grade plutonium is to fabricate it into fuel and use it for generation of electrical energy in commercial nuclear power plants. Weapons-grade plutonium can be used as fuel in existing commercial nuclear power plants, such as those in the US and Russia. This recovers energy and economic value from weapons-grade plutonium, which otherwise represents a large cost liability to maintain in safeguarded and secure storage. The plutonium remaining in spent MOX fuel is reactor-grade, essentially the same as that being discharged in spent UO 2 fuels. MOX fuels are well developed and are currently used in a number of LWRs in Europe. Plutonium-bearing fuels without uranium (non-fertile fuels) would require some development. However, such non-fertile fuels are attractive from a nonproliferation perspective because they avoid the insitu production of additional plutonium and enhance the annihilation of the plutonium inventory on a once-through fuel cycle

Preparation of plutonium fluoride to obtain metal of high purity; Preparation de fluorures de plutonium pour l'obtention de metal de haute purete

Energy Technology Data Exchange (ETDEWEB)

Faugeras, P; Brut, A; Helou, R [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

1960-07-01

In the process of treating irradiated uranium, plutonium can be separated from the majority of the fission products and from the uranium by TBP extraction cycles. The high purity necessary for metallurgical and nuclear physics experiments led us to consider more elaborate purification processes, and a specially adapted method of fluoride preparation. The first part of the paper describes purification cycles of plutonium in solution on ion exchange resins, and the results are given. The second part contains the description and results of the fluoride preparation method. (author) [French] Dans le processus du traitement de l'uranium irradie, les cycles d'extraction au TBP permettent la separation du plutonium de la majorite des produits de fission et de l'uranium. La haute purete exigee pour les experiences de metallurgie et de physique nucleaire nous a conduit a envisager des purifications plus poussee et un mode de confection des fluorures specialement adapte. La premiere partie de l'expose decrit et donne les resultats de cycles de purification du plutonium en solution sur des resines echangeuses d'ions. La seconde partie decrit et donne les resultats du mode de confection des fluorures. (auteur)

Internal stresses in α-plutonium during deformation

International Nuclear Information System (INIS)

Merz, M.D.

1976-01-01

Internal stresses were measured in fine grained (2 μm) and coarse grained (20 μm) α-plutonium. In the fine grained metal the internal stress sigmasub(i), which was interpreted as the stress driving recovery processes near grain boundaries, was weakly dependent on applied stress, sigmasub(a). The effective stress, sigmasub(e) = sigma sub(a) - sigmasub(i), which is the stress to move dislocations, increased nearly 1:1 with applied stress, especially at high applied stresses. The strain rate obeyed the relation epsilon=K(T)sigmasub(e)sup(n) where K(T) is a temperature dependent term and n approximately = 3. The recovery rate in fine grained α-plutonium during creep was concluded to be very sensitive to internal stress. The internal stress in α-plutonium with 20 μm grain size was much higher than in the finer grain metal. (Auth.)

233-S Plutonium Concentration Facility data quality objectives

International Nuclear Information System (INIS)

Encke, D.B.

1996-08-01

This document is a summary of the decision-making associated with the Data Quality Objective process that pertains to the characterization activities in the 233-S Plutonium Concentration Facility at the Hanford Site in Richland, Washington. The 233-S Plutonium Concentration Facility is located adjacent to, and north of, the REDOX Plant. The facility was used to concentrate the plutonium nitrate product solution from the REDOX facility. The 233-S Pipe Gallery, Control Room, SWP Change Room, Toilet, Equipment Room and the Electrical Cubicle are currently scheduled for decontamination and cleanout to support future demolition (D and D). Identification of the radiological contamination and presence of hazardous materials is needed to allow for disposal of the D and D debris

Safely disposing and controlling the various forms of excess military plutonium

International Nuclear Information System (INIS)

Albright, D.

1991-01-01

The growing surplus of plutonium will continue to pose safety, health, and verification problems. Although long term storage and disposal of plutonium seems technically feasible, or at least comparable in technical difficulty to commercial spent fuel disposal, significant political obstacles within the government and the public, may make it difficult to solve this problem. Although options to build verifiable warhead dismantlement facilities or to recycle plutonium in reactors and thus convert separated plutonium into irradiated fuel are straight forward concepts, their realization remains difficult for economic and political reasons. The plutonium recycle option also raises additional proliferation concerns about its impact on civilian nuclear programs. In the absence of a long term solution, the United States can implement various storage or interim disposal options that involve minimal processing, but that ease verification problems and provide adequate safety and protection of public health

The toxicity of plutonium

International Nuclear Information System (INIS)

Crouse, P.L.

1994-01-01

Shipments of plutonium occasionally pass around the Cape coastal waters on its way to Japan from Europe. This invariably leads to a great deal of speculation of the dangers involved and of the extreme toxicity of plutonium, with the media and environmental groups claiming that (a) plutonium is the most toxic substance known to man, and that (b) a few kilograms of plutonium ground finely and dispersed in the atmosphere could kill every human being on earth. Comparisons with other poisons are drawn, e.g. common inorganic chemicals and biological agents. The original scare around the extraordinary toxicity of Pu seems to have started in 1974 with the claims of Tamplin and Cochran's hot particle theory about plutonium lodging in the sensitive portions of the lungs in small concentrated aggregates where they are much more effective in producing cancers. This theory, however, is regarded as thoroughly discredited by the experts in the field of radiotoxicity. 8 refs

Review of Sodium and Plutonium related Technical Standards in Trans-Uranium Fuel Fabrication Facilities

Energy Technology Data Exchange (ETDEWEB)

Jang, Misuk; Jeon, Jong Seon; Kang, Hyun Sik; Kim, Seoung Rae [NESS, Daejeon (Korea, Republic of)

2016-10-15

In this paper, we would introduce and review technical standards related to sodium fire and plutonium criticality safety. This paper may be helpful to identify considerations in the development of equipment, standards, and etc., to meet the safety requirements in the design, construction and operating of TFFF, KAPF and SFR. The feasibility and conceptual designs are being examined on related facilities, for example, TRU Fuel Fabrication Facilities (TFFF), Korea Advanced Pyro-process Facility (KAPF), and Sodium Cooled Fast Reactor (SFR), in Korea. However, the safety concerns of these facilities have been controversial in part because of the Sodium fire accident and Plutonium related radiation safety caused by transport and handling accident. Thus, many researches have been performed to ensure safety and various documents including safety requirements have been developed. In separating and reducing the long-lived radioactive transuranic(TRU) in the spent nuclear fuel, reusing as the potential energy of uranium fuel resources and reducing the high level wastes, TFFF would be receiving the attention of many people. Thus, people would wonder whether compliance with technical standards that ensures safety. For new facility design, one of the important tasks is to review of technical standards, especially for sodium and Plutonium because of water related highly reactive characteristics and criticality hazard respectively. We have introduced and reviewed two important technical standards for TFFF, which are sodium fire and plutonium criticality safety, in this paper. This paper would provide a brief guidance, about how to start and what is important, to people who are responsible for the initial design to operation of TFFF.

Review of Sodium and Plutonium related Technical Standards in Trans-Uranium Fuel Fabrication Facilities

International Nuclear Information System (INIS)

Jang, Misuk; Jeon, Jong Seon; Kang, Hyun Sik; Kim, Seoung Rae

2016-01-01

In this paper, we would introduce and review technical standards related to sodium fire and plutonium criticality safety. This paper may be helpful to identify considerations in the development of equipment, standards, and etc., to meet the safety requirements in the design, construction and operating of TFFF, KAPF and SFR. The feasibility and conceptual designs are being examined on related facilities, for example, TRU Fuel Fabrication Facilities (TFFF), Korea Advanced Pyro-process Facility (KAPF), and Sodium Cooled Fast Reactor (SFR), in Korea. However, the safety concerns of these facilities have been controversial in part because of the Sodium fire accident and Plutonium related radiation safety caused by transport and handling accident. Thus, many researches have been performed to ensure safety and various documents including safety requirements have been developed. In separating and reducing the long-lived radioactive transuranic(TRU) in the spent nuclear fuel, reusing as the potential energy of uranium fuel resources and reducing the high level wastes, TFFF would be receiving the attention of many people. Thus, people would wonder whether compliance with technical standards that ensures safety. For new facility design, one of the important tasks is to review of technical standards, especially for sodium and Plutonium because of water related highly reactive characteristics and criticality hazard respectively. We have introduced and reviewed two important technical standards for TFFF, which are sodium fire and plutonium criticality safety, in this paper. This paper would provide a brief guidance, about how to start and what is important, to people who are responsible for the initial design to operation of TFFF

Plutonium use in foreign countries (03)

International Nuclear Information System (INIS)

Otagaki, Takao

2004-03-01

European countries and Japan had been implementing the strategy of spent fuel reprocessing in order to use nuclear material to the maximum. Plutonium recovered from reprocessing, however, must be recycle on light water reactors (LWRs) because of considerable delay of fast reactor development. In Europe, much of experiences of plutonium recycling have been accumulated until now. Thus, the status of plutonium recycling up to the end of 2003 in France, Germany, The U.K., Belgium, Switzerland and other countries were studied based on the following scope. (1) Basic policy and present status of plutonium recycling in primary countries of France, Germany, The U.K., Belgium, Switzerland, and Sweden which plans to recycle a part of plutonium: Backend policy and the status of spent fuel management were studied, then integrated analysis and evaluation of the position of plutonium recycling in backend and the status of plutonium recycling development were performed. (2) Plan and experience of Mixed Oxide (MOX) fuel fabrication and reprocessing of spent fuels: The data and information on plan and experience of MOX fuel fabrication and reprocessing in foreign countries were collected. (3) Plutonium inventories: The data and information of plutonium inventories of foreign countries were collected. (author)

Cigarette smoke and plutonium

International Nuclear Information System (INIS)

Filipy, R.E.

1983-01-01

The major objective of this project is to obtain experimental data that are directly applicable to resolving the question of whether cigarette smokers are at greater risk than nonsmokers to potential health effects of inhaled plutonium. Because cigarette smokers constitute a large fraction of the population, a synergistic effect of plutonium and cigarette smoke might influence estimates of the health risk for plutonium and other transuranics released to the environment

Cycle downstream: the plutonium question

International Nuclear Information System (INIS)

Zask, G.; Rome, M.; Delpech, M.

1998-01-01

This day, organized by the SFEN, took place at Paris the 4 june 1998. Nine papers were presented. They take stock on the plutonium physics and its utilization as a nuclear fuel. This day tried to bring information to answer the following questions: do people have to keep the plutonium in the UOX fuel or in the MOX fuel in order to use it for future fast reactors? Do people have to continue obstinately the plutonium reprocessing in the MOX for the PWR type reactors? Will it be realized a underground disposal? Can it be technically developed plutonium incinerators and is it economically interesting? The plutonium physics, the experimental programs and the possible solutions are presented. (A.L.B.)

Closure Welding of Plutonium Bearing Storage Containers

International Nuclear Information System (INIS)

Cannell, G.R.

2002-01-01

A key element in the Department of Energy (DOE) strategy for the stabilization, packaging and storage of plutonium-bearing materials involves closure welding of DOE-STD-3013 Outer Containers (3013 container). The 3013 container provides the primary barrier and pressure boundary preventing release of plutonium-bearing materials to the environment. The final closure (closure weld) of the 3013 container must be leaktight, structurally sound and meet DOE STD 3013 specified criteria. This paper focuses on the development, qualification and demonstration of the welding process for the closure welding of Hanford PFP 3013 outer containers

Plutonium Immobilization Can Loading Preliminary Specifications

Energy Technology Data Exchange (ETDEWEB)

Kriikku, E.

1998-11-25

This report discusses the Plutonium Immobilization can loading preliminary equipment specifications and includes a process block diagram, process description, equipment list, preliminary equipment specifications, plan and elevation sketches, and some commercial catalogs. This report identifies loading pucks into cans and backfilling cans with helium as the top priority can loading development areas.

Aqueous Solution Chemistry of Plutonium

Energy Technology Data Exchange (ETDEWEB)

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

2014-01-28

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

Plutonium Proliferation: The Achilles Heel of Disarmament

International Nuclear Information System (INIS)

Leventhal, Paul

2001-01-01

Plutonium is a byproduct of nuclear fission, and it is produced at the rate of about 70 metric tons a year in the world's nuclear power reactors. Concerns about civilian plutonium ran high in the 1970s and prompted enactment of the Nuclear Non-Proliferation Act of 1978 to give the United States a veto over separating plutonium from U.S.-supplied uranium fuel. Over the years, however, so-called reactor-grade plutonium has become the orphan issue of nuclear non-proliferation, largely as a consequence of pressures from plutonium-separating countries. The demise of the fast breeder reactor and the reluctance of utilities to introduce plutonium fuel in light-water reactors have resulted in large surpluses of civilian, weapons-usable plutonium, which now approach in size the 250 tons of military plutonium in the world. Yet reprocessing of spent fuel for recovery and use of plutonium proceeds apace outside the United States and threatens to overwhelm safeguards and security measures for keeping this material out of the hands of nations and terrorists for weapons. A number of historical and current developments are reviewed to demonstrate that plutonium commerce is undercutting efforts both to stop the spread of nuclear weapons and to work toward eliminating existing nuclear arsenals. These developments include the breakdown of U.S. anti-plutonium policy, the production of nuclear weapons by India with Atoms-for-Peace plutonium, the U.S.-Russian plan to introduce excess military plutonium as fuel in civilian power reactors, the failure to include civilian plutonium and bomb-grade uranium in the proposed Fissile Material Cutoff Treaty, and the perception of emerging proliferation threats as the rationale for development of a ballistic missile defense system. Finally, immobilization of separated plutonium in high-level waste is explored as a proliferation-resistant and disarmament-friendly solution for eliminating excess stocks of civilian and military plutonium.

Gamma ray NDA assay system for total plutonium and isotopics in plutonium product solutions

International Nuclear Information System (INIS)

Cowder, L.R.; Hsue, S.T.; Johnson, S.S.; Parker, J.L.; Russo, P.A.; Sprinkle, J.K.; Asakura, Y.; Fukuda, T.; Kondo, I.

1979-01-01

A LASL-designed gamma-ray NDA instrument for assay of total plutonium and isotopics of product solutions at Tokai-Mura is currently installed and operating. The instrument is, optimally, a densitometer that uses radioisotopic sources for total plutonium measurements at the K absorption edge. The measured transmissions of additional gamma-ray lines from the same radioisotopic sources are used to correct for self-attenuation of passive gamma rays from plutonium. The corrected passive data give the plutonium isotopic content of freshly separated to moderately aged solutions. This off-line instrument is fully automated under computer control, with the exception of sample positioning, and operates routinely in a mode designed for measurement control. A one-half percent precision in total plutonium concentration is achieved with a 15-minute measurement

An autoradiographical method using an imaging plate for the analyses of plutonium contamination in a plutonium handling facility

International Nuclear Information System (INIS)

Takasaki, Koji; Sagawa, Naoki; Kurosawa, Shigeyuki; Mizuniwa, Harumi

2011-01-01

An autoradiographical method using an imaging plate (IP) was developed to analyze plutonium contamination in a plutonium handling facility. The IPs were exposed to ten specimens having a single plutonium particle. Photostimulated luminescence (PSL) images of the specimens were taken using a laser scanning machine. One relatively large spot induced by α-radioactivity from plutonium was observed in each PSL image. The plutonium-induced spots were discriminated by a threshold derived from background and the size of the spot. A good relationship between the PSL intensities of the spots and α-radioactivities measured using a radiation counter was obtained by least-square fitting, taking the fading effect into consideration. This method was applied to workplace monitoring in an actual uranium-plutonium mixed oxide (MOX) fuel fabrication facility. Plutonium contaminations were analyzed in ten other specimens having more than two plutonium spots. The α-radioactivities of plutonium contamination were derived from the PSL images and their relative errors were evaluated from exposure time. (author)

Characterization of transuranic solid wastes from a plutonium processing facility

International Nuclear Information System (INIS)

Mulkin, R.

1975-06-01

Transuranic-contaminated wastes generated in the processing areas of the Plutonium Chemistry and Metallurgy Group at the Los Alamos Scientific Laboratory (LASL) were studied in detail to identify their chemical and physical composition. Nondestructive Assay (NDA) equipment was developed to measure transuranic activity at the 10-nCi/g level in low-density residues typically found in room-generated waste. This information will supply the Waste Management Program with a more positive means of identifying concerns in waste storage and the challenge of optimizing the system of waste form, packaging, and environment of the storage area for 20-yr retrievable waste. A positive method of measuring transuranic activity in waste at the 10-nCi/g level will eliminate the need for administrative control in a sensitive area, and will provide the economic advantage of minimizing the volume of waste stored as retrievable waste. (U.S.)

Development of the plutonium oxide vitrification system