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

Oxidation-state distribution of plutonium in surface and subsurface waters at Thule, northwest Greenland

International Nuclear Information System (INIS)

McMahon, C.A.; Leon Vintro, L.; Mitchell, P.I.; Dahlgaard, H.

2000-01-01

The speciation of plutonium in Arctic waters sampled on the northwest Greenland shelf in August 1997 is discussed in this paper. Specifically, we report the results of analyses carried out on seawater sampled (a) close to the Thule air base where, in 1968, a US military aircraft carrying four nuclear weapons crashed on sea ice, releasing kilogram quantities of plutonium to the snow pack and underlying seabed sediments, and (b) at a reference station (Upernavik) located ∼400 km to the south. The data show that most of the plutonium in the dissolved phase at Thule is in the form of Pu(V, VI) (mean: 68±6%; n=6), with little if any distinction apparent between surface and bottom waters. Further, the oxidation state distribution at stations close to the accident site is similar to that measured at Upernavik, remote from this site. It is also similar to the distribution observed in shelf waters at mid-latitudes, suggesting that the underlying processes controlling plutonium speciation are insensitive to temperature over the range 0-25 deg. C. Measurements using tangential-flow ultrafiltration indicate that virtually all of the plutonium (including the fraction in a reduced chemical form) is present as fully dissolved species. Most of this plutonium would seem to be of weapons fallout origin, as the mean 238 Pu/ 239,240 Pu activity ratio in the water column (dissolved phase) at Thule (0.06±0.02; n=10) is similar to the global fallout ratio at this latitude (∼0.04). Thus, there is little evidence of weapons-grade plutonium in the water column at Thule at the present time

Bulging of cans containing plutonium residues. Summary report

International Nuclear Information System (INIS)

Van Konynenburg, R.A.; Wood, D.H.; Condit, R.H.; Shikany, S.D.

1996-03-01

In 1994, two cans in the Lawrence Livermore National Laboratory Plutonium Facility were found to be bulging as a result of the generation of gases form the plutonium ash residues contained in the cans. This report describes the chronology of this discovery, the response actions that revealed other pressurized cans, the analysis of the causes, the short-term remedial action, a followup inspection of the short-term storage packages, and a review of proposed long-term remedial options

``Distribution and behaviour of plutonium in the waters of the channel and of the seine estuary``; ``Distribution et comportement du plutonium dans les eaux de la manche et de l`estuaire de la seine``

Energy Technology Data Exchange (ETDEWEB)

Garcia, K

1998-12-31

Excess dissolved plutonium has been measured in the coastal waters of the Channel, from Granville to Boulogne, probably due to sorption-desorption processus. In the Seine estuary, in situ measurements and experimental studies showed that the plutonium desorbs himself from particles in low salinity waters. The desorbed plutonium originates in marine and/or fluvial dissolved Pu. Marine dissolved Pu(V), originating from La Hague plant discharges and from atlantic waters, is reduced and sorbed when the salinity decreases onto estuarial particles: Isotopic Activity Ration {sup 238}Pu/{sup 239}, Pu(IR) of marine dissolved Pu(V) is about 0.7. Fluvial dissolved plutonium originates from atmospheric fallout and from an internal river source: fallout plutonium (IR=0.05) is unreactive with salinity while 45% of river plutonium (IR>1.7) flocculates at 0.5 g l{sup -1}. Desorbed plutonium may have various origins, depending on the Seine liquid discharges and on the tidal coefficient. When the marine waters do not migrate upstream, the low salinity waters encounters particles marked essentially with marine plutonium and the IR of desorbed Pu is about 0.7. The activities of desorbed plutonium are too low to have any influence on the distribution of plutonium in the coastal waters on the Seine Bay. When the marine waters migrate upstream, the low salinity waters meet particles marked essentially with river plutonium (IR>1.7) and desorbed plutonium has a very high IR. These estuarine conditions are encountered five to seven month a year and implicate an increase of the IR of 0.1 of the plutonium present in the coastal waters of the Seine bay (1.2.-1.3.). (author).

The effect of state of health on organ distribution and excretion of systemic plutonium in the Mayak workers

International Nuclear Information System (INIS)

Suslova, K.G.; Khokhryakov, V.F.; Tokarskaya, Z.B.; Nifatov, A.P.; Sokolova, A.B.; Kudryavtzeva, T.I.; Miller, S.C.; Krahenbuhl, M.P.

2003-01-01

The extrapulmonary distribution of plutonium in 20 organs (excluding the respiratory tract) was studied in workers who chronically inhaled plutonium at the radiochemical plants of the Mayak Production Association (Ozyorsk, Russia). The data were obtained by radiochemical analysis of soft tissue and bones samples collected at autopsy of 591 workers. The systemic plutonium distribution was determined in healthy individuals as well as in those with health impairment, specifically for those with liver diseases. Twenty-five years after the beginning of inhalation, systemic fractions in the liver and skeleton of individuals who were healthy at the time of death approximate the ratio 45%:45% proposed in the International Commission on Radiological Protection (ICRP) Publication 30. Pathological process in the liver, accompanied by fatty dystrophy of hepatocytes, increased plutonium clearance from the liver. There was a considerable shift of the plutonium from the liver to the skeleton in individuals who died from liver disease. The average fractions of systemic plutonium in the liver and skeleton of those individuals were 14% and 78% respectively, which did not correspond to ICRP models, indicating a significant effect of disease conditions. Plutonium that was not redistributed was excreted. The urinary excretion rate of plutonium also correlated with state of health. The observed excretion as a fraction of systemic content was 1.64 x 10 -5 d -1 for individuals of good health and 2.34 x 10 -5 d -1 for individuals with various chronic diseases. The current models do not account for the influence of different pathological processes in the body on plutonium distribution and retention in systemic organs. This could have significant consequences for dosimetry calculations and risk estimations. (author)

Oxidation-state distribution of plutonium in surface and subsurface waters at Thule, northwest Greenland

DEFF Research Database (Denmark)

McMahon, C.A.; Vintró, L.L.; Mitchell, P.I.

2000-01-01

(V, VI) (mean, 68 +/- 6%; n = 6), with little if any distinction apparent between surface and bottom waters. Further, the oxidation state distribution at stations close to the accident site is similar to that measured at Upernavik, remote from this site. It is also similar to the distribution observed...... in shelf waters at midlatitudes, suggesting that the underlying processes controlling plutonium speciation are insensitive to temperature over the range 0-25 degrees C. Measurements using tangential-flow ultrafiltration indicate that virtually all of the plutonium (including the fraction in a reduced...... chemical form) is present as fully dissolved species. Most of this plutonium would seem to be of weapons fallout origin, as the mean Pu-238/Pu-239,Pu-240 activity ratio in the water column (dissolved phase) at Thule (0.06 +/- 0.02; n = 10) is similar to the global fallout ratio at this latitude...

Biochemical fractionation and cellular distribution of americium and plutonium in the biomass of freshwater macrophytes

International Nuclear Information System (INIS)

Zotina, T.A.; Kalacheva, G.S.; Bolsunovsky, A.Ya.

2011-01-01

Accumulation of americium ( 241 Am) and plutonium ( 238,242 Pu) and their distribution in cell compartments and biochemical components of the biomass of freshwater aquatic plants Elodea canadensis, Ceratophyllum demersum and Myrioplyllum spicatum and aquatic moss Fontinalis antipyretica have been investigated in laboratory experiments. Americium and plutonium taken up from water by Elodea canadensis apical shoots were mainly absorbed by structural components of plant cells (90% for 241 Am; 89% for 238 Pu and 82-87% for 242 Pu). About 10-18% of isotope activity was recorded in the cytosol fraction. The major concentration (76-92%) of americium was bound to cell wall cellulose-like polysaccharides of Elodea canadensis, Myriophyllum spicatum, Ceratophyllum demersum and Fontinalis antipyretica, 8-24% of americium activity was registered in the fraction of proteins and carbohydrates, and just a minor concentration (<1%) in the lipid fraction. The distribution of plutonium in the biomass fractions of Elodea was similar to that of americium. Hence, americium and plutonium had the highest affinity to cellulose-like polysaccharides of cell walls of freshwater submerged macrophytes. (author)

The distribution of plutonium in the mouse ovary

International Nuclear Information System (INIS)

Green, D.; Howells, G.; Vennart, J.; Watts, R.

1977-01-01

Twelve-week old female CBA mice were injected intravenously with an ultra-filtered solution of 239 Pu in 1% trisodium citrate and were killed at intervals up to 180 days. The plutonium in the ovaries was measured radiochemically and autoradiographically. The fractional content of injected activity and daily absorbed dose showed no significant variation with time after injection. At early times after injection, α-tracks from the 239 Pu were randomly distributed over all the tissues, with concentrations of tracks occurring over some atretic follicles. By 180 days, the random distribution of tracks was much reduced, and discrete clusters of tracks were in evidence. The possible risk of genetic damage is discussed. (author)

''Distribution and behaviour of plutonium in the waters of the channel and of the seine estuary''

International Nuclear Information System (INIS)

Garcia, K.

1997-01-01

Excess dissolved plutonium has been measured in the coastal waters of the Channel, from Granville to Boulogne, probably due to sorption-desorption processus. In the Seine estuary, in situ measurements and experimental studies showed that the plutonium desorbs himself from particles in low salinity waters. The desorbed plutonium originates in marine and/or fluvial dissolved Pu. Marine dissolved Pu(V), originating from La Hague plant discharges and from atlantic waters, is reduced and sorbed when the salinity decreases onto estuarial particles: Isotopic Activity Ration 238 Pu/ 239 , Pu(IR) of marine dissolved Pu(V) is about 0.7. Fluvial dissolved plutonium originates from atmospheric fallout and from an internal river source: fallout plutonium (IR=0.05) is unreactive with salinity while 45% of river plutonium (IR>1.7) flocculates at 0.5 g l -1 . Desorbed plutonium may have various origins, depending on the Seine liquid discharges and on the tidal coefficient. When the marine waters do not migrate upstream, the low salinity waters encounters particles marked essentially with marine plutonium and the IR of desorbed Pu is about 0.7. The activities of desorbed plutonium are too low to have any influence on the distribution of plutonium in the coastal waters on the Seine Bay. When the marine waters migrate upstream, the low salinity waters meet particles marked essentially with river plutonium (IR>1.7) and desorbed plutonium has a very high IR. These estuarine conditions are encountered five to seven month a year and implicate an increase of the IR of 0.1 of the plutonium present in the coastal waters of the Seine bay (1.2.-1.3.). (author)

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

Plutonium distribution in various components of natural organic matters and their role in plutonium migration in soils

Energy Technology Data Exchange (ETDEWEB)

Pavlotskaya, F.I.; Goryachenkova, T.A.

1987-09-01

The purpose of this work was to ascertain the links of plutonium with various components of the organic matter of different types of soils and their role in its migration in soils. The test objects were typical soils of forest and forest-steppe zones: sod-podzolic, gray forest, and leached chernozem contaminated with plutonium under laboratory conditions and stored in the air-dried state for three years, as also chernozem leached from an experimental site where agricultural plants were grown for a long time. The plutonium content in the fractions isolated from the contaminated soils was determined by its direct coprecipitation with microgram quantities of cerium hydroxide. The chemical yield of plutonium was determined by adding to a solution aliquot, equal to the analysis aliquot in volume, a known amount of plutonium and by its isolation under identical conditions. The ..gamma..-radiation of plutonium isolated on a nuclear filter with a pore size less than or equal to 15 ..mu..m was measured on a Protoka type gas flow counter.

Plutonium: An introduction

International Nuclear Information System (INIS)

Condit, R.H.

1993-10-01

This report is a summary of the history and properties of plutonium. It presents information on the atoms, comparing chemical and nuclear properties. It looks at the history of the atom, including its discovery and production methods. It summarizes the metallurgy and chemistry of the element. It also describes means of detecting and measuring the presence and quantity of the element

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)

Plutonium safety training course

International Nuclear Information System (INIS)

Moe, H.J.

1976-03-01

This course seeks to achieve two objectives: to provide initial safety training for people just beginning work with plutonium, and to serve as a review and reference source for those already engaged in such work. Numerous references have been included to provide information sources for those wishing to pursue certain topics more fully. The first part of the course content deals with the general safety approach used in dealing with hazardous materials. Following is a discussion of the four properties of plutonium that lead to potential hazards: radioactivity, toxicity, nuclear properties, and spontaneous ignition. Next, the various hazards arising from these properties are treated. The relative hazards of both internal and external radiation sources are discussed, as well as the specific hazards when plutonium is the source. Similarly, the general hazards involved in a criticality, fire, or explosion are treated. Comments are made concerning the specific hazards when plutonium is involved. A brief summary comparison between the hazards of the transplutonium nuclides relative to 239 Pu follows. The final portion deals with control procedures with respect to contamination, internal and external exposure, nuclear safety, and fire protection. The philosophy and approach to emergency planning are also discussed

Summary report of the grazing studies conducted on a plutonium-contaminated range in Area 13 of the Nevada Test Site

International Nuclear Information System (INIS)

Smith, D.D.

1979-05-01

Actinide concentrations in the tissues of beef animals periodically sacrificed and sampled during a 3-year grazing study on a plutonium-contaminated range of the Nevada Test Site are tabulated and discussed. The primary objective of this study was to determine the uptake and tissue distribution of the plutonium by ruminants. Food habit analyses of ingesta from rumen-fistulated steers and sacrificed cattle revealed that shrub species made up the major portion of their diet during most seasons of the year. Grasses were preferred during the spring months. Using activity levels found in the rumen contents, it was estimated that a study cow ingested 100 microcuries of plutonium-239 prior to sacrifice. Of this, 16.4 microcuries was in rumen fluids from which a combined retention factor of 0.0034% was calculated for the bone, muscle, and liver. Comparisons of plutonium-239/plutonium-238 ratios in ingesta and tissues indicate that the plutonium-238 is more readily absorbed and retained. No radiologically significant lesions were found. The gonadal concentrations of the actinides were significantly higher than those of blood and muscle and approached those of bone. These data indicate that consideration should be given to the plutonium-239 dose to gonads as well as that to bone, liver, and lungs of man. Actinide concentrations of animals born in the study areas showed an increasing trend with time. Concentrations of plutonium-239 in the lung, liver, muscle, and femur tissues of the Area 13 cattle were significantly higher than in tissues collected from grazing cattle from other sites. The plutonium-239 concentrations in bones, lungs, and livers collected from wildlife with free access to and from the contaminated zones reflect the dilution resulting from these animals ranging into the less contaminated areas around the study sites

Distribution of moisture, tritium, and plutonium in the alluvium, aquifer, and underlying tuff in Mortandad Canyon

International Nuclear Information System (INIS)

Purtymun, W.D.; Maes, M.N.; Peters, R.

1985-01-01

A study of the distribution of moisture, tritium, and plutonium in the Mortandad Canyon aquifer indicates some infiltration of water into the underlying tuff. This infiltration was accompanied by similar movement of tritium. The concentrations of plutonium on the sediments in the aquifer were low when compared with the high concentrations in solution in an ionic complex that does not readily exchange or is adsorbed by clay minerals in the alluvium. 2 references, 4 figures, 2 tables

Charge distribution on plutonium-containing aerosols produced in mixed-oxide reactor fuel fabrication and the laboratory

International Nuclear Information System (INIS)

Yeh, H.C.; Newton, G.J.; Teague, S.V.

1976-01-01

The inhalation toxicity of potentially toxic aerosols may be affected by the electrostatic charge on the particles. Charge may influence the deposition site during inhalation and therefore its subsequent clearance and dose patterns. The electrostatic charge distributions on plutonium-containing aerosols were measured with a miniature, parallel plate, aerosol electrical mobility spectrometer. Two aerosols were studied: a laboratory-produced 238 PuO 2 aerosol (15.8 Ci/g) and a plutonium mixed-oxide aerosol (PU-MOX, natural UO 2 plus PuO 2 , 0.02 Ci/g) formed during industrial centerless grinding of mixed-oxide reactor fuel pellets. Plutonium-238 dioxide particles produced in the laboratory exhibited a small net positive charge within a few minutes after passing through a 85 Kr discharger due to alpha particle emission removal of valence electrons. PU-MOX aerosols produced during centerless grinding showed a charge distribution essentially in Boltzmann equilibrium. The gross alpha aerosol concentrations (960-1200 nCi/l) within the glove box were sufficient to provide high ion concentrations capable of discharging the charge induced by mechanical and/or nuclear decay processes

Disposal of Surplus Weapons Grade Plutonium

International Nuclear Information System (INIS)

Alsaed, H.; Gottlieb, P.

2000-01-01

The Office of Fissile Materials Disposition is responsible for disposing of inventories of surplus US weapons-usable plutonium and highly enriched uranium as well as providing, technical support for, and ultimate implementation of, efforts to obtain reciprocal disposition of surplus Russian plutonium. On January 4, 2000, the Department of Energy issued a Record of Decision to dispose of up to 50 metric tons of surplus weapons-grade plutonium using two methods. Up to 17 metric tons of surplus plutonium will be immobilized in a ceramic form, placed in cans and embedded in large canisters containing high-level vitrified waste for ultimate disposal in a geologic repository. Approximately 33 metric tons of surplus plutonium will be used to fabricate MOX fuel (mixed oxide fuel, having less than 5% plutonium-239 as the primary fissile material in a uranium-235 carrier matrix). The MOX fuel will be used to produce electricity in existing domestic commercial nuclear reactors. This paper reports the major waste-package-related, long-term disposal impacts of the two waste forms that would be used to accomplish this mission. Particular emphasis is placed on the possibility of criticality. These results are taken from a summary report published earlier this year

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

Surplus plutonium disposition environmental impact statement. Public scoping meeting: Comment summary report

International Nuclear Information System (INIS)

1997-09-01

The Department of Energy (DOE) issued a Record of Decision for the Storage and Disposition of Weapons-Usable Fissile Materials Programmatic Environmental Impact Statement (S ampersand D PEIS) (DOE/EIS-0229) on January 14, 1997. In that Record of Decision, DOE stated its decision to pursue a strategy for plutonium disposition that allows for immobilization of surplus weapons plutonium in glass or ceramic forms and irradiating the surplus plutonium as mixed oxide (MOX) fuel in existing reactors, while reserving the option to immobilize all the surplus weapons plutonium. The Department also decided that the extent to which either or both of these disposition approaches would ultimately be deployed would depend in part upon future National Environmental Policy Act (NEPA) review for surplus weapons plutonium disposition. On May 22, 1997, DOE published in the Federal Register (62 FR 28013) a Notice of Intent to prepare an environmental impact statement (tiered from the S ampersand D PEIS) on the disposition of United States' surplus weapons-usable plutonium. The purpose of the Notice of Intent was to describe DOE's proposed action, to solicit public input, and to announce the schedule for the public scoping meetings. During the public scoping period (May 22 - July 22, 1997), the public was invited to submit written comments by U.S. mail, fax, or through the Office of Fissile Materials Disposition's Website, as well as to provide oral comments by voicemail or by participating in public scoping meetings. Written and oral comments on the scope of the SPD EIS that were submitted during the formal comment period have been uniquely identified and have become part of the official record. This is the case whether the comments were submitted via U.S. mail, fax, website, toll-free telephone number, or through participation at a public scoping meeting

Distribution coefficients for plutonium and americium on particulates in aquatic environments

International Nuclear Information System (INIS)

Sanchez, A.L.; Schell, W.R.; Sibley, T.H.

1982-01-01

The distribution coefficients of two transuranic elements, plutonium and americium, were measured experimentally in laboratory systems of selected freshwater, estuarine, and marine environments. Gamma-ray emitting isotopes of these radionuclides, 237 Pu and 241 Am, were significantly greater than the sorption Ksub(d) values, suggesting some irreversibility in the sorption of these radionuclides onto sediments. The effects of pH and of sediment concentration on the distribution coefficients were also investigated. There were significant changes in the Ksub(d) values as these parameters were varied. Experiments using sterilized and nonsterilized samples for some of the sediment/water systems indicate possible bacterial effects on Ksub(d) values. (author)

Excess Weapons Plutonium Immobilization in Russia

International Nuclear Information System (INIS)

Jardine, L.; Borisov, G.B.

2000-01-01

The joint goal of the Russian work is to establish a full-scale plutonium immobilization facility at a Russian industrial site by 2005. To achieve this requires that the necessary engineering and technical basis be developed in these Russian projects and the needed Russian approvals be obtained to conduct industrial-scale immobilization of plutonium-containing materials at a Russian industrial site by the 2005 date. This meeting and future work will provide the basis for joint decisions. Supporting R and D projects are being carried out at Russian Institutes that directly support the technical needs of Russian industrial sites to immobilize plutonium-containing materials. Special R and D on plutonium materials is also being carried out to support excess weapons disposition in Russia and the US, including nonproliferation studies of plutonium recovery from immobilization forms and accelerated radiation damage studies of the US-specified plutonium ceramic for immobilizing plutonium. This intriguing and extraordinary cooperation on certain aspects of the weapons plutonium problem is now progressing well and much work with plutonium has been completed in the past two years. Because much excellent and unique scientific and engineering technical work has now been completed in Russia in many aspects of plutonium immobilization, this meeting in St. Petersburg was both timely and necessary to summarize, review, and discuss these efforts among those who performed the actual work. The results of this meeting will help the US and Russia jointly define the future direction of the Russian plutonium immobilization program, and make it an even stronger and more integrated Russian program. The two objectives for the meeting were to: (1) Bring together the Russian organizations, experts, and managers performing the work into one place for four days to review and discuss their work with each other; and (2) Publish a meeting summary and a proceedings to compile reports of all the

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)

Plutonium distribution and remobilization in sediments of the Rhone River mouth (North-Western Mediterranean); Distribution et remobilisation du plutonium dans les sediments du prodelta du Rhone (Mediterranee nord-occidentale)

Energy Technology Data Exchange (ETDEWEB)

Lansard, B

2004-06-15

The aim of the present study was to describe the distribution and remobilization of plutonium (Pu) in the sediments off the Rhone river mouth. Most of the {sup 238}Pu and {sup 239,240}Pu isotopes introduced into the Rhone River were discharged by the liquid effluents released from the Marcoule reprocessing plant, located 120 km upstream the river mouth. Due to its high affinity for particles and its long half life, {sup 238}Pu is a promising tracer to follow the dispersion of particulate matter from the Rhone River to the Mediterranean Sea. During the 3 REMORA cruises, sediment samples were specifically collected in the Rhone pro-delta area and more offshore on the whole continental shelf of the Gulf of Lions. The measurements of alpha emitters gave a first detailed spatial distribution of Pu isotope concentrations in surface sediments off the Rhone mouth. Using {sup 137}Cs concentrations and their correlations with Pu isotopes, we were able to give a first estimate of Pu inventories for the sediments of the study area. In 2001, plutonium inventories were estimated to 92 {+-} 7 GBq of {sup 238}Pu and 522 {+-} 44 GBq of {sup 239,240}Pu for an area of 500 km{sup 2} in front of the Rhone River mouth. Roughly, 50 % of these inventories are trapped in an area of 100 km{sup 2} corresponding to the extent of the Rhone pro-delta zone. In spring 2002, an ADCP, with current velocity and wave measurements, was moored off the Rhone River mouth. This unique in situ dataset highlights the major role of South-East swells in the erosion of pro-deltaic sediments and their dispersion to the South-Westward direction. Plutonium remobilization was examined using a new experimental design based on sediment resuspension processes studied within a linear recirculating flume. For Gulf of Lions sediments and for a given hydrodynamic stress, remobilization fluxes raised a maximum of 0.08 Bq.m{sup -2}.h{sup -1} for {sup 238}Pu and 0.64 Bq.m{sup -2}.h{sup -1} for {sup 239,240}Pu. A first

Summary of the Nevada Applied Ecology Group and correlative programs

International Nuclear Information System (INIS)

Friesen, H.N.

1992-10-01

This summary document presents results in a broad context; it is not limited to findings of the Nevada Applied Ecology Group. This book is organized to present the findings of the Nevada Applied Ecology Group and correlative programs in accordance with the originally stated objectives of the Nevada Applied Ecology Group. This plan, in essence, traces plutonium from its injection into the environment to movement in the ecosystem to development of cleanup techniques. Information on other radionuclides was also obtained and will be presented briefly. Chapter 1 presents a brief description of the ecological setting of the Test Range Complex. The results of investigations for plutonium distribution are presented in Chapter 2 for the area surrounding the Test Range Complex and in Chapter 3 for on-site locations. Chapters 4 and 5 present the results of investigations concerned with concentrations and movement, respectively, of plutonium in the ecosystem of the Test Range Complex, and Chapter 6 summarizes the potential hazard from this plutonium. Development of techniques for cleanup and treatment is presented in Chapter 7, and the inventory of radionuclides other than plutonium is presented briefly in Chapter 8

Current status of the plutonium hot particle problem

International Nuclear Information System (INIS)

Richmond, C.R.

1975-01-01

Information now available on the question of lung irradiation from particulate plutonium is reviewed. Careful consideration of the available data shows that particulate plutonium is not more hazardous than the same amount of plutonium distributed uniformly. The data also suggest that the potential hazard from plutonium increases as the dispersion throughout the lung becomes more uniform

Comparison of the distribution coefficients of plutonium and other radionuclides in Lake Michigan to those in other systems

International Nuclear Information System (INIS)

Wahlgren, M.A.; Nelson, D.M.

1976-01-01

Filtration of Lake Michigan water samples has been carried out routinely since 1973, and some plutonium concentrations in the seston have been reported. During 1975 and 1976 a sufficient number of filter samples from various depths was obtained throughout the field seasons to establish whether or not a distribution coefficient also controls the uptake of plutonium by the formation of particulates and their settling from the surface waters. Samples from ANL station 5 (10 km SW of Grand Haven, Michigan, water depth 67 m), of the southern basin, and from the lower Great Lakes have been analyzed for dry weight, ash weight, total organic (loss of weight on ignition), amorphous silica, calcite, and residual minerals. Distribution coefficients were calculated on the basis of each of these solid components, and self-consistent values were observed for depth, season, or lake only, on the basis of dry weight of seston. The findings strongly suggest that the uptake of fallout plutonium (including inputs of new fallout during the summer of 1975) is dominated by a surface coating process common to all seston particle types. An insufficient number of 137 Cs analyses were obtained to correlate its uptake to a specific component of the seston, but its behavior is clearly different from that of plutonium

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.)

Amarillo National Resource Center for Plutonium. Quarterly technical progress report, May 1, 1997--July 31, 1997

Energy Technology Data Exchange (ETDEWEB)

NONE

1997-09-01

Progress summaries are provided from the Amarillo National Center for Plutonium. Programs include the plutonium information resource center, environment, public health, and safety, education and training, nuclear and other material studies.

The comparative distribution of thorium and plutonium in human tissues

International Nuclear Information System (INIS)

Singh, Narayani P.; Shawki Amin Ibrahim; Cohen, Norman; Wrenn, McDonald E.

1978-01-01

Thorium is the most chemically and biologically similar natural element to the manmade element plutonium. Both are actinides, and for both the most stable valency state is +4, and solubility in natural body fluids is low. They are classified together in ICRP Lung Model. The present paper deals with the question of whether or not the analogy between the two actinides in terms of deposition and retention in human tissues is a good one. Preliminary results on the thorium contents ( 228,230 Th and 232 Th) of three sets of human tissues from a western U.S. town containing a uranium tailings pile are compared with the reported values of plutonium content of human tissues from the general populations who are exposed to environmental plutonium from fallout of nuclear detonations. Samples were taken at autopsy where sudden death had occurred. For the three isotopes of thorium, the ratio of the content of each (pCi/organ, normalized by organ weight to ICRP Reference Man) in lung to lymph nodes varies from 2-25 for individuals with a mean of 8; this is similar to that we infer from the literature for 239 , 240 Pu which suggests a ratio of lung to lymph nodes with a mean of approximately 7. However, the relative thorium contents of lung and liver are dissimilar, lung/liver for thorium being 3.5 and for plutonium 0.2 to 0.1. Similarly, the ratios of thorium and plutonium content of liver and bone vary significantly; the ratio for thorium is 0.1 and for plutonium 0.8 to 0.5. The most significant observation at this stage is that the relative accumulation of thorium in human liver is much less than that of plutonium. Some of the plausible reasons will be discussed. (author)

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

The radial distribution of plutonium in high burnup UO2 fuels

International Nuclear Information System (INIS)

Lassmann, K.; O'Carroll, C.; Laar, J. van de; Walker, C.T.

1994-01-01

A new model (TUBRNP) is described which predicts the radial power density distribution as a function of burnup (and hence the radial burnup profile as a function of time) together with the radial profile of uranium and plutonium isotopes. Comparisons between measurements and the predictions of the TUBRNP model are made on fuels with enrichments in the range 2.9 to 8.25% and with burnups between 21 000 and 64 000 MWd/t. It is shown to be in excellent agreement with experimental measurements and is a marked improvement on earlier versions. (orig.)

Summary of plutonium terrestrial research studies in the vicinity of a nuclear fuel reprocessing plant

International Nuclear Information System (INIS)

Corey, J.C.; Boni, A.L.; Andriano, D.C.; Pinder, J.F.; McLeod, K.W.

1978-01-01

This paper reports plutonium concentrations of wheat, soybeans, and corn grown (a) on a field adjacent to one of the nuclear reprocessing facilities at the Savannah River Plant (SRP), (b) in a glasshouse, and (c) offsite. The crops on SRP were grown on a field that has been receiving both fallout plutonium and plutonium emitted at low chronic levels from an air exhaust stack since 1955. The crops grown in the glasshouse were raised on soil from the onsite agricultural field. The offsite field has received only fallout plutonium. The crop data indicate that the dose to an individual from ingesting grain grown on the field, although higher than from ingesting grain grown offsite, is still small (the 70-year dose-to-bone from eating 2 X 10 5 g (440 lb) of wheat in a year would be less than one mrem). Crop data from the field and the glasshouse experiment indicate that less than 10% of the total contamination of field-grown crops adjacent to a reprocessing facility was contributed by root uptake, the remainder by deposition on the plant surfaces. The plutonium content of the grain was generally 10 to 100 times less than that of the vegetation, again suggesting that deposition from stack emissions vegetation, again suggesting that deposition from stack emissions on the vegetation increased the plutonium content; whereas the grain, particularly corn and soybeans, was protected by thehusk or pod and contained principally plutonium from the root uptake pathway

Elaboration and characterisation of plutonium waste reference materials

International Nuclear Information System (INIS)

Perolat, J.P.

1990-01-01

The Analysis Methods Establishment Commission (CETAMA) has set up a program for the elaboration and characterisation of plutonium waste reference materials. The object of this program is to give laboratories the possibility to test and calibrate apparatus used in non-destructive methods for the analysis of plutonium waste. The different parameters of this program are presented: - characterisation of plutonium, - type and number of containers, - plutonium distribution inside the different containers, - description of the matrix

Routes of plutonium uptake and their relation to biomagnification in starfish

International Nuclear Information System (INIS)

Guary, J.-C.; Fowler, S.W.; Beasley, T.M.

1982-01-01

The distribution of 239+240 Pu and 238 Pu in environmental samples of starfish tissues is identical to the tissue distribution observed in experimental animals following uptake of plutonium directly from water. Plutonium in sea water has a strong affinity for the mucus-rich epidermal layer of starfish which contributes substantially to the relatively high levels of this transuranium nuclide measured in these invertebrates. Transfer of plutonium to starfish via food also occurs; however, the resultant tissue distribution is not consistent with that found in the natural environment where plutonium is available from both contaminated food and water. These data suggest that food chain biomagnification of plutonium by starfish does not occur in nature as has been previously hypothesized. (author)

Contamination of living environment and human organism with plutonium

International Nuclear Information System (INIS)

Benes, J.

1981-01-01

The applicability of 239 Pu in nuclear power is discussed. The radiotoxic properties of plutonium, its tissue distribution and the effects of internal and external contamination are described. The contamination of the atmosphere, water, and soil with plutonium isotopes is discussed. Dosimetry is described of plutonium in the living and working environments as is plutonium determination in the human organism. (H.S.)

Summary of the Nevada Applied Ecology Group and correlative programs. Version 1

Energy Technology Data Exchange (ETDEWEB)

Friesen, H.N. [Raytheon Services Nevada, Las Vegas, NV (United States)

1992-10-01

This summary document presents results in a broad context; it is not limited to findings of the Nevada Applied Ecology Group. This book is organized to present the findings of the Nevada Applied Ecology Group and correlative programs in accordance with the originally stated objectives of the Nevada Applied Ecology Group. This plan, in essence, traces plutonium from its injection into the environment to movement in the ecosystem to development of cleanup techniques. Information on other radionuclides was also obtained and will be presented briefly. Chapter 1 presents a brief description of the ecological setting of the Test Range Complex. The results of investigations for plutonium distribution are presented in Chapter 2 for the area surrounding the Test Range Complex and in Chapter 3 for on-site locations. Chapters 4 and 5 present the results of investigations concerned with concentrations and movement, respectively, of plutonium in the ecosystem of the Test Range Complex, and Chapter 6 summarizes the potential hazard from this plutonium. Development of techniques for cleanup and treatment is presented in Chapter 7, and the inventory of radionuclides other than plutonium is presented briefly in Chapter 8.

PWR benchmarks. From OECD working party on physics of plutonium recycling

International Nuclear Information System (INIS)

Bernnat, W.; Lutz, D.; Sartori, E.; Schlosser, G.; Cathalau, S.; Soldevila, M.

1995-01-01

A two year study organised by the OECD/NEACOGEMA on the physics of plutonium recycle (Working Party on the Physics of Plutonium Recycle - WPPR) has just completed its final report. The study reviewed the important aspects of the physics of plutonium recycle in Pressurised Water Reactors (PWRs), Bolling Water reactors (BWRs) and fast reactors. The final report includes a description and analysis of the results of three physical benchmark exercises which were specified for PWRs and two for fast reactors. This paper presents a summary of the most important observations and conclusions from the PWR benchmark exercises. (authors)

Inventory calculations in sediment samples with heterogeneous plutonium activity distribution

International Nuclear Information System (INIS)

Eriksson, M.; Dahlgaard, H.

2002-01-01

A method to determine the total inventory of a heterogeneously distributed contamination of marine sediments is described. The study site is the Bylot Sound off the Thule Airbase, NW Greenland, where marine sediments became contaminated with plutonium in 1968 after a nuclear weapons accident. The calculation is based on a gamma spectrometric screening of the 241 Am concentration in 450 one-gram aliquots from 6 sediment cores. A Monte Carlo programme then simulates a probable distribution of the activity, and based on that, a total inventory is estimated by integrating a double exponential function. The present data indicate a total inventory around 3.5 kg, which is 7 times higher than earlier estimates (0.5 kg). The difference is partly explained by the inclusion of hot particles in the present calculation. A large uncertainty is connected to this estimate, and it should be regarded as preliminary. (au)

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.

Inhaled plutonium oxide in dogs

International Nuclear Information System (INIS)

Anon.

1981-01-01

This project is concerned with long-term experiments to determine the life-span dose-effect relationships of inhaled 239 PuO 2 and 238 PuO 2 in beagles. The data will be used to estimate the health effects of inhaled transuranics. The tissue distribution of plutonium, radiation effects in the lung and hematologic changes in plutonium-exposed beagles with lung tumors were evaluated

Plutonium distribution and remobilization in sediments of the Rhone River mouth (North-Western Mediterranean)

International Nuclear Information System (INIS)

Lansard, B.

2004-06-01

The aim of the present study was to describe the distribution and remobilization of plutonium (Pu) in the sediments off the Rhone river mouth. Most of the 238 Pu and 239,240 Pu isotopes introduced into the Rhone River were discharged by the liquid effluents released from the Marcoule reprocessing plant, located 120 km upstream the river mouth. Due to its high affinity for particles and its long half life, 238 Pu is a promising tracer to follow the dispersion of particulate matter from the Rhone River to the Mediterranean Sea. During the 3 REMORA cruises, sediment samples were specifically collected in the Rhone pro-delta area and more offshore on the whole continental shelf of the Gulf of Lions. The measurements of alpha emitters gave a first detailed spatial distribution of Pu isotope concentrations in surface sediments off the Rhone mouth. Using 137 Cs concentrations and their correlations with Pu isotopes, we were able to give a first estimate of Pu inventories for the sediments of the study area. In 2001, plutonium inventories were estimated to 92 ± 7 GBq of 238 Pu and 522 ± 44 GBq of 239,240 Pu for an area of 500 km 2 in front of the Rhone River mouth. Roughly, 50 % of these inventories are trapped in an area of 100 km 2 corresponding to the extent of the Rhone pro-delta zone. In spring 2002, an ADCP, with current velocity and wave measurements, was moored off the Rhone River mouth. This unique in situ dataset highlights the major role of South-East swells in the erosion of pro-deltaic sediments and their dispersion to the South-Westward direction. Plutonium remobilization was examined using a new experimental design based on sediment resuspension processes studied within a linear recirculating flume. For Gulf of Lions sediments and for a given hydrodynamic stress, remobilization fluxes raised a maximum of 0.08 Bq.m -2 .h -1 for 238 Pu and 0.64 Bq.m -2 .h -1 for 239,240 Pu. A first plutonium budget determined for the study area indicates that at least 85

Accident investigation board report on the May 14, 1997, chemical explosion at the Plutonium Reclamation Facility, Hanford Site,Richland, Washington - summary report

International Nuclear Information System (INIS)

Gerton, R.E.

1997-01-01

This report is a summary of the Accident Investigation Board Report on the May 14, 1997, Chemical Explosion at the Plutonium Reclamation Facility, Hanford Site, Richland, Washington (DOE/RL-97-59). The referenced report provides a greater level of detail and includes a complete discussion of the facts identified, analysis of those facts, conclusions derived from the analysis, identification of the accident's causal factors, and recommendations that should be addressed through follow-up action by the U.S. Department of Energy and its contractors. This companion document provides a concise summary of that report, with emphasis on management issues. Evaluation of emergency and occupational health response to, and radiological and chemical releases from, this accident was not within the scope of this investigation, but is the subject of a separate investigation and report (see DOE/RL-97-62)

Model of plutonium dynamics in a deciduous forest ecosystem

International Nuclear Information System (INIS)

Garten, C.T. Jr.; Gardner, R.H.; Dahlman, R.C.

1980-01-01

A linear compartment model with donor-controlled flows between compartments was designed to describe and simulate the behavior of plutonium ( 239 240 Pu) in a contaminated forest ecosystem at Oak Ridge, TN. At steady states predicted by the model, less than 0.25% of the plutonium in the ecosystem resides in biota. Soil is the major repository of plutonium in the forest, and exchanges of plutonium between soil and litter or soil and tree roots were dominant transfers affecting the ecosystem distribution of plutonium. Variation in predicted steady-state amounts of plutonium in the forest, given variability in the model parameters, indicates that our ability to develop models of plutonium transport in ecosystems should improve with greater precision in data from natural environments and a better understanding of sources of variation in plutonium data

What we have learned about plutonium from human data

International Nuclear Information System (INIS)

Voelz, G.L.

1975-01-01

Human data of plutonium deposition, internal distribution, and excretion have been obtained by observations after accidental occupational exposures, long-term follow-up studies on plutonium workers, and autopsy tissue analyses. No significant harmful effects have been noted in humans, although a small foreign-body type nodule around dermal implantations of plutonium has been described in eight persons. Methods used to estimate body burdens by urinary excretion values appear to be conservative generally compared to autopsy tissue burdens. Variations in autopsy tissue distribution appear to be related to the conditions of the plutonium exposure including mode of exposure, particle size, chemical composition, solubility in serum or tissue fluids, and time after exposure for internal redistribution. An important conclusion of this human data survey is the recognition of the inestimable value to be gained by continued careful studies on the life history of workers with higher plutonium exposures. (author)

Environmental plutonium levels near the Nevada Test Site

International Nuclear Information System (INIS)

Bliss, W.A.; Jakubowski, F.M.

1977-01-01

The Environmental Monitoring and Support Laboratory-Las Vegas is engaged in a study to define the distribution of plutonium in the environment surrounding the Nevada Test Site (NTS). Extensive soil sampling has been conducted around the NTS, both to define areal distribution and to investigate local concentrating effects by natural phenomena. Additionally, air filters used in the off-NTS air surveillance network as well as those collected in special studies have been analyzed for plutonium to better define ambient levels and to investigate the possibility of resuspension. Results of these, as well as other studies related to defining the ambient plutonium levels around the NTS, are given in this report

Dissolution and transport of plutonium from oxide particles in soils

International Nuclear Information System (INIS)

Brown, D.A.

1978-01-01

This report contains a summary of methods and data on plutonium dissolution and movement in four soils, plus a copy of a manuscript describing the automatic sample changer for alpha radiation detection which has been submitted for publication

Validation of the TUBRNP model with the radial distribution of plutonium in MOX fuel measured by SIMS and EPMA

Energy Technology Data Exchange (ETDEWEB)

O` Carroll, C; Laar, J Van De; Walker, C T [CEC Joint Research Centre, Karlsruhe (Germany)

1997-08-01

The new model TUBRNP (TRANSURANUS burnup) predicts the radial power density distribution as a function of burnup (and hence the radial burnup profile as a function of time) together with the radial profile of plutonium. Comparisons between measurements and the prediction of the TUBRNP model have been made for UO{sub 2} LWR fuels: they were found to be in excellent agreement and it is seen that TUBRNP is a marked improved on previous models. A powerful techniques for the characterization of irradiation fuel is Electron Probe Microanalysis (EPMA). Uranium, plutonium and fission product distributions can be analysed quantitatively. A complement, providing isotopic information with a lateral resolution comparable to EPMA, is secondary ion mass spectrometry (SIMS). Recently, the technique has been successfully applied for the measurement of the radial distribution of plutonium isotopes in irradiated nuclear fuel pins. The extension of the TUBRNP model to mixed oxide fuels seems to be the natural step to take. In MOX fuels the picture is greatly complicated by the presence of the (U, Pu)O{sub 2} agglomerates. The rim effect referred to above may be masked by the high concentrations of plutonium in the bulk of the fuel. A detailed investigation of a number of MOX fuel samples has been made using the TUBRNP model. Results are presented for a range of fuels with different enrichment and burnup. Through its participation in the PRIMO and DOMO programmes, PSI in conjunction with the Institute for Transuranium Elements had the opportunity to validate the new theoretical model TUBRNP. The authors with therefore to express their thanks to the organizers and to the numerous European and Japanese organizations which have supported these two international programmes on MOX fuel behavior. 7 refs, 9 figs, 3 tabs.

Long term performance session summary

Energy Technology Data Exchange (ETDEWEB)

Hanauer, S.

1996-05-01

This paper presents brief summaries of reports given on plutonium disposal. Topics include: performance of waste forms; glass leaching; ceramic leaching; safeguards and security issues; safeguards of vitrification; and proliferation risks of geologic disposal.

Studies of plutonium in human tracheobronchial lymph nodes

International Nuclear Information System (INIS)

McInroy, J.F.; Stewart, M.W.; Moss, W.D.

1976-01-01

Since 1959, tissues from 70 occupationally exposed former employees of the Los Alamos Scientific Laboratory have been examined following autopsy. Exposure in most cases was to inhaled plutonium oxide aerosols. Chemical analyses of selected tissues were performed to determine the amount of plutonium retained in the body at the time of death. On the basis of the measured tissue concentrations of plutonium, extrapolations of total-body burdens were made. Thirty-three of the measured cases had plutonium depositions in the tracheobronchial lymph nodes ranging from 0.1 to 4000 dpm per gram of tissue (0.05 to 1800 pCi/g). The duration of exposures ranged from 4 to 30 years. Microscopic examination of representative sections of these lymph nodes revealed no abnormalities other than those which were directly attributable to the basic disease that caused the demise of the various persons in this study. The size distribution of plutonium particles in nodes from one individual was determined by exposing tissue sections to nuclear track film. The estimated mass median diameter of the particles was 0.3 μm, and the distribution had a geometric standard deviation of 1.6. It is estimated that 95 percent of the individual particles had corresponding plutonium concentrations between 0.001 and 0.22 pCi

Phenomenology of uranium-plutonium homogenization in nuclear fuels

International Nuclear Information System (INIS)

Marin, J.M.

1988-01-01

The uranium and plutonium cations distribution in mixed oxide fuels (U 1-y Pu y )O 2 with y ≤ 0.1 has been studied in laboratory with industrial fabrication methods. Our experiences has showed a slow cations migration. In the substoichiometry (UPu)O 2-x the diffusion is in connection with the plutonium valence which is an indicator of the oxidoreduction state of the crystal lattice. The plutonium valence is in connection with the oxygen ion deficit in order to compensate the electrical charge. The oxygen ratio of the solid depends of the oxygen partial pressure prevailing at the time of product elaboration but it can be modified by impurities. These impurities permit to increase or decrease the fuel characteristics and performances. An homogeneity analysis methodology is proposed, its objective is to classify the mixed oxide fuels according to the uranium and plutonium ions distribution [fr

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.

Plutonium spot of mixed oxide fuel, 2

International Nuclear Information System (INIS)

Suzuki, Yukio; Maruishi, Yoshihiro; Satoh, Masaichi; Aoki, Toshimasa; Muto, Tadashi

1974-01-01

In a fast reactor, the specification for the homogeneity of plutonium in plutonium-uranium mixed-oxide fuel is mainly dependent on the nuclear characteristics, whereas in a thermal reactor, on thermal characteristics. This homogeneity is measured by autoradiography as the plutonium spot size of the specimens which are arbitrarily chosen fuel pellets from a lot. Although this is a kind of random sampling, it is difficult to apply this method to conventional digital standards including JIS standards. So a special sampling inspection method was studied. First, it is assumed that the shape of plutonium spots is spherical, the size distribution is logarithmic normal, and the standard deviation is constant. Then, if standard deviation and mean spot size are given, the logarithmic normal distribution is decided unitarily, and further if the total weight of plutonium spots for a lot of pellets is known, the number of the spots (No) which does not conform to the specification can be obtained. Then, the fraction defective is defined as No devided by the number of pellets per lot. As to the lot with such fraction defective, the acceptance coefficient of the lot was obtained through calculation, in which the number of sampling, acceptable diameter limit observed and acceptable conditions were used as parameters. (Tai, I.)

Fission fragment mass and total kinetic energy distributions of spontaneously fissioning plutonium isotopes

Science.gov (United States)

Pomorski, K.; Nerlo-Pomorska, B.; Bartel, J.; Schmitt, C.

2018-03-01

The fission-fragment mass and total kinetic energy (TKE) distributions are evaluated in a quantum mechanical framework using elongation, mass asymmetry, neck degree of freedom as the relevant collective parameters in the Fourier shape parametrization recently developed by us. The potential energy surfaces (PES) are calculated within the macroscopic-microscopic model based on the Lublin-Strasbourg Drop (LSD), the Yukawa-folded (YF) single-particle potential and a monopole pairing force. The PES are presented and analysed in detail for even-even Plutonium isotopes with A = 236-246. They reveal deep asymmetric valleys. The fission-fragment mass and TKE distributions are obtained from the ground state of a collective Hamiltonian computed within the Born-Oppenheimer approximation, in the WKB approach by introducing a neck-dependent fission probability. The calculated mass and total kinetic energy distributions are found in good agreement with the data.

Distribution and identification of Plutonium(IV) species in tri-n-butyl phosphate/HNO3 extraction system containing acetohydroxamic acid

International Nuclear Information System (INIS)

Tkac, P.; Paulenova, A.; Vandegrift, G.F.; Krebs, J.F.

2009-01-01

There was a significant research progress achieved with the aim to modify conventional PUREX process by stripping of plutonium from the tri-n-butyl phosphate (TBP) extraction product in the form of non-extractable complexes upon addition of back-hold complexation agents. The present paper reports effects of such salt-free complexant, acetohydroxamic acid (HAHA), on distribution ratio of Pu(IV) under wide concentration of nitric acid and additional nitrate. General formula of plutonium species present in the organic phase can be described as Pu(OH) x (AHA) y (NO3) 4-x-y x 2TBP x wHNO 3 . (author)

Physics of Plutonium Recycling in Thermal Reactors

International Nuclear Information System (INIS)

Kinchin, G.H.

1967-01-01

A substantial programme of experimental reactor physics work with plutonium fuels has been carried out in the UK; the purpose of this paper is to review the experimental and theoretical work, with emphasis on plutonium recycling in thermal reactors. Although the main incentive for some of the work may have been to study plutonium build-up in uranium-fuelled reactors, it is nevertheless relevant to plutonium recycling and no distinction is drawn between build-up and enrichment studies. A variety of techniques have been for determining reactivity, neutron spectrum and reaction rates in simple assemblies of plutonium-aluminium fuel with water, graphite and beryllia moderators. These experiments give confidence in the basic data and methods of calculation for near-homogeneous mixtures of plutonium and moderator. In the practical case of plutonium recycling it is necessary to confirm that satisfactory predictions can be made for heterogeneous lattices enriched with plutonium. In this field, experiments have been carried out with plutonium-uranium metal and oxide-cluster fuels in graphite-moderated lattices and in SGHW lattices, and the effects of 240 Pu have been studied by perturbation measurements with single fuel elements. The exponential and critical experiments have used tonne quantities of fuel with plutonium contents ranging from 0.25 to 1.2% and the perturbation experiments have extended both the range of plutonium contents and the range of isotopic compositions of plutonium. In addition to reactivity and reactivity coefficients, such as the temperature coefficients, attention has been concentrated on relative reaction rate distributions which provide evidence for variations of neutron spectrum. .Theoretical comparisons, together with similar comparisons for non-uniform lattices, establish the validity of methods of calculation which have been used to study the feasibility of plutonium recycling in thermal reactors. (author)

Physics of Plutonium Recycling in Thermal Reactors

Energy Technology Data Exchange (ETDEWEB)

Kinchin, G. H. [Atomic Energy Establishment, Winfrith, Dorchester, Dorset (United Kingdom)

1967-09-15

A substantial programme of experimental reactor physics work with plutonium fuels has been carried out in the UK; the purpose of this paper is to review the experimental and theoretical work, with emphasis on plutonium recycling in thermal reactors. Although the main incentive for some of the work may have been to study plutonium build-up in uranium-fuelled reactors, it is nevertheless relevant to plutonium recycling and no distinction is drawn between build-up and enrichment studies. A variety of techniques have been for determining reactivity, neutron spectrum and reaction rates in simple assemblies of plutonium-aluminium fuel with water, graphite and beryllia moderators. These experiments give confidence in the basic data and methods of calculation for near-homogeneous mixtures of plutonium and moderator. In the practical case of plutonium recycling it is necessary to confirm that satisfactory predictions can be made for heterogeneous lattices enriched with plutonium. In this field, experiments have been carried out with plutonium-uranium metal and oxide-cluster fuels in graphite-moderated lattices and in SGHW lattices, and the effects of {sup 240}Pu have been studied by perturbation measurements with single fuel elements. The exponential and critical experiments have used tonne quantities of fuel with plutonium contents ranging from 0.25 to 1.2% and the perturbation experiments have extended both the range of plutonium contents and the range of isotopic compositions of plutonium. In addition to reactivity and reactivity coefficients, such as the temperature coefficients, attention has been concentrated on relative reaction rate distributions which provide evidence for variations of neutron spectrum. .Theoretical comparisons, together with similar comparisons for non-uniform lattices, establish the validity of methods of calculation which have been used to study the feasibility of plutonium recycling in thermal reactors. (author)

Plutonium Chemistry in the UREX Separation Processes

International Nuclear Information System (INIS)

Paulenova, Alena; Vandegrift, George F. III; Czerwinski, Kenneth R.

2009-01-01

The objective of the project is to examine the chemical speciation of plutonium in UREX+ (uranium/tributylphosphate) extraction processes for advanced fuel technology. Researchers will analyze the change in speciation using existing thermodynamics and kinetic computer codes to examine the speciation of plutonium in aqueous and organic phases. They will examine the different oxidation states of plutonium to find the relative distribution between the aqueous and organic phases under various conditions such as different concentrations of nitric acid, total nitrates, or actinide ions. They will also utilize techniques such as X-ray absorbance spectroscopy and small-angle neutron scattering for determining plutonium and uranium speciation in all separation stages. The project started in April 2005 and is scheduled for completion in March 2008.

Alternative technical summary report for immobilized disposition in deep boreholes: Immobilized disposal of plutonium in coated ceramic pellets in grout without canisters, Version 4.0. Fissile materials disposition program

International Nuclear Information System (INIS)

Wijesinghe, A.M.

1996-01-01

This paper summarizes and compares the immobilized and direct borehole disposition alternatives previously presented in the alternative technical summary. The important design concepts, facility features and operational procedures are first briefly described. This is followed by a discussion of the issues that affect the evaluation of each alternative against the programmatic assessment criteria that have been established for selecting the preferred alternatives for plutonium disposition

Alternative technical summary report for immobilized disposition in deep boreholes: Immobilized disposal of plutonium in coated ceramic pellets in grout without canisters, Version 4.0. Fissile materials disposition program

Energy Technology Data Exchange (ETDEWEB)

Wijesinghe, A.M.

1996-08-23

This paper summarizes and compares the immobilized and direct borehole disposition alternatives previously presented in the alternative technical summary. The important design concepts, facility features and operational procedures are first briefly described. This is followed by a discussion of the issues that affect the evaluation of each alternative against the programmatic assessment criteria that have been established for selecting the preferred alternatives for plutonium disposition.

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)

Distribution of plutonium amongst and within selected bones from an injection case

International Nuclear Information System (INIS)

Larsen, R.P.; Oldham, R.D.; Martin, S.M.

1979-01-01

The burden and macrodistribution of plutonium in the skeleton of a man who received 0.38 μCi of 239 Pu by injection were determined. The relative concentrations in the bones analyzed are comparable to those obtained in a study of another subject. The concentrations in the trabecular and cortical portions of these bones were determined; the concentration ratio ranged from 1.9 to 4.7. The data show that (1) within a bone the plutonium concentration in the trabecular portion is always higher than it is in the cortical portion, but (2) within a group of bones plutonium concentration is not correlated with degree of trabecularity

Deposition and retention of plutonium in the United States general population

International Nuclear Information System (INIS)

McInroy, J.F.; Boyd, H.A.; Eutsler, B.C.

1979-01-01

Since 1959, a Los Alamos National Laboratory study has analyzed over 5000 tissues from 1100 individuals of the nonoccupationally exposed general population for fallout plutonium. These data have been useful in determining the tissue distributions and the annual baseline levels of environmental plutonium in the United States population. The effects of age, sex, date of death, cause of death and geographic location of resididence on the observed plutonium deposition have been evaluated. Because of the difference in biological turnover times of plutonium in the various organs of the body and the changing concentrations of plutonium in the atmosphere, the plutonium concentration ratios between tissues have changed as a function of time. However, our data indicate that over the past 10 years, the highest concentrations in the general population are found in the tracheobronchial lymph nodes and the liver and the lowest concentrations are in the spleen, gonads and kidney. The median body burdens of plutonium in the US population are estimated to have reached 12 pCi during the 1960's and have declined to about 2 pCi in 1977. Large errors in estimated skeletal burdens of plutonium may exist because of small specimen sample sizes and a lack of knowledge concerning the relative distribution of plutonium among the various bones of the human body

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

Fabrication of mixed oxide fuel using plutonium from dismantled weapons

International Nuclear Information System (INIS)

Blair, H.T.; Chidester, K.; Ramsey, K.B.

1996-01-01

A very brief summary is presented of experimental studies performed to support the use of plutonium from dismantled weapons in fabricating mixed oxide (MOX) fuel for commercial power reactors. Thermal treatment tests were performed on plutonium dioxide powder to determine if an effective dry gallium removal process could be devised. Fabrication tests were performed to determine the effects of various processing parameters on pellet quality. Thermal tests results showed that the final gallium content is highly dependent on the treatment temperature. Fabrication tests showed that the milling process, sintering parameters, and uranium feed did effect pellet properties. 1 ref., 1 tab

Plutonium Chemistry in the UREX+ Separation Processes

Energy Technology Data Exchange (ETDEWEB)

ALena Paulenova; George F. Vandegrift, III; Kenneth R. Czerwinski

2009-10-01

The project "Plutonium Chemistry in the UREX+ Separation Processes” is led by Dr. Alena Paulenova of Oregon State University under collaboration with Dr. George Vandegrift of ANL and Dr. Ken Czerwinski of the University of Nevada at Las Vegas. The objective of the project is to examine the chemical speciation of plutonium in UREX+ (uranium/tributylphosphate) extraction processes for advanced fuel technology. Researchers will analyze the change in speciation using existing thermodynamics and kinetic computer codes to examine the speciation of plutonium in aqueous and organic phases. They will examine the different oxidation states of plutonium to find the relative distribution between the aqueous and organic phases under various conditions such as different concentrations of nitric acid, total nitrates, or actinide ions. They will also utilize techniques such as X-ray absorbance spectroscopy and small-angle neutron scattering for determining plutonium and uranium speciation in all separation stages. The project started in April 2005 and is scheduled for completion in March 2008.

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

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.)

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)

Plutonium in Southern Hemisphere Ocean Waters

Energy Technology Data Exchange (ETDEWEB)

Hirose, K. [Sophia University, Tokyo (Japan); Aoyama, M. [Meteorological Research Institute, Tsukuba (Japan); Gastaud, J.; Levy, I. [Marine Environment Laboratories, International Atomic Energy Agency (Monaco); Fukasawa, M. [Japan Agency for Marine-Earth Science and Technology Yokosuka (Japan); Kim, C. -S. [Environment Laboratories, International Atomic Energy Agency, Seibersdorf (Austria); Povinec, P. P. [Comenius University, Bratislava (Slovakia); Roos, P. [Riso National Laboratory, Roskilde (Denmark); Sanchez-Cabeza, J. A. [Universitat Autonoma de Barcelona, Bellaterra (Spain); Yim, S. A. [Korea Institute of Nuclear Safety, Daejeon (Korea, Republic of)

2013-07-15

Plutonium in seawater collected by the BEAGLE2003 cruise was determined using ICP-SF-MS and alpha spectrometry after Fe co-precipitation and radiochemical purification. Levels and distributions of dissolved plutonium activity concentrations in Southern Hemisphere ocean waters are summarized here, including historical data. Pu-239 concentrations in surface water of the central South Pacific (32.5{sup o}S) in 2003 were around 1 mBq/m{sup 3}. The {sup 239}Pu concentrations in the Indian Ocean surface waters (20{sup o}S) were similar to that in the South Pacific, whereas the {sup 239}Pu concentrations in the South Atlantic surface waters (30{sup o}S) were markedly lower than those in the South Pacific and Indian Oceans. The {sup 239}Pu vertical profile pattern was similar to that in the North Pacific subtropical gyre, although {sup 239}Pu concentrations in the deep South Pacific were significantly lower than those in the North Pacific. One of the dominant factors controlling plutonium distributions in the Southern Hemisphere oceans is biogeochemical processes including particle scavenging. (author)

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

Plutonium in the arctic marine environment--a short review.

Science.gov (United States)

Skipperud, Lindis

2004-06-18

Anthropogenic plutonium has been introduced into the environment over the past 50 years as the result of the detonation of nuclear weapons and operational releases from the nuclear industry. In the Arctic environment, the main source of plutonium is from atmospheric weapons testing, which has resulted in a relatively uniform, underlying global distribution of plutonium. Previous studies of plutonium in the Kara Sea have shown that, at certain sites, other releases have given rise to enhanced local concentrations. Since different plutonium sources are characterised by distinctive plutonium-isotope ratios, evidence of a localised influence can be supported by clear perturbations in the plutonium-isotope ratio fingerprints as compared to the known ratio in global fallout. In Kara Sea sites, such perturbations have been observed as a result of underwater weapons tests at Chernaya Bay, dumped radioactive waste in Novaya Zemlya, and terrestrial runoff from the Ob and Yenisey Rivers. Measurement of the plutonium-isotope ratios offers both a means of identifying the origin of radionuclide contamination and the influence of the various nuclear installations on inputs to the Arctic, as well as a potential method for following the movement of water and sediment loads in the rivers.

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

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

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

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)

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

Summary of recent studies of soil plutonium in the Los Alamos and Trinity Site environs

International Nuclear Information System (INIS)

Nyhan, J.W.; Hakonson, T.E.

1976-01-01

The first plutonium was sent to the Los Alamos Scientific Laboratory (LASL) in 1944 from the Oak Ridge and Hanford reactors for use in synthesizing the first atomic bomb, which was subsequently detonated at Trinity Site in New Mexico. During the last 32 years the LASL has developed an outstanding capability in many scientific fields required to support research in weapons technology and in other uses of nuclear energy. The fabrication and experimental activities required for this effort have resulted in additions of plutonium in industrial effluents to Los Alamos soils, just as the Trinity soils received fallout plutonium after the 1945 Trinity detonation. Formal radioecology-soils studies relative to soil-actinide relationships has been mainly field-oriented and complements transuranic research dealing with the biota of several study areas. The current soil actinide research performed within three liquid effluent-receiving areas at Los Alamos and along the fallout pathway of Trinity, the first nuclear detonation, are summarized

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.

Study on plutonium distribution in Palomares ecosystem after an accidental aerosol release of transuranic radionuclides

International Nuclear Information System (INIS)

Gasco Sanchez, L.

1990-01-01

A discharge of plutonium and transuranic elements accidentally ocurred near Palomares (Almeria, Spain) in 1966. After decontamining operations, about 10 g of finely dispersed plutonium remained on the soil and was spreaded on the sorroundings and into Mediterranean sea. An analytical study including a 34 sampling sites of marine sediments, chemical clean-up, analytical methods for isolating plutonium from interfering radionuclides in the alfa-spectra was carried out. The detection limit level reached for the 239 u+ 240 Pu was 10 mBq/Kg one of the lowest cited in the Spanish analytical literature until now. These results were attained following a careful electroplating Pu deposition method developed by our laboratory as result of the high signal/noise rates measured and a 20 KeV resolution. Several analytical assurance quality procedures specially developed for the Palomares ecological system were applied to the results, at the CIEMAT laboratories using reference standard certified samples. The values were unbiased and with no differences statistically significants between them. Interlaboratory comparisons were carried out. After 20 years of plutonium traces environmental transport their concentration were from two at three times the leves of radionuclides in the fallout of the zone studied. The plutonium concentration range in surface sediments was 0.3-5.0 Bq/Kg. The highest values corresponding in the coastal sediments and the lowest in the deep sea. Plutonium concentrations are highly correlated with the sediments structure, grain size composition and distance from the mouth of Almanzora river. The most important contribution at the transport from the land into sea could be the freshet occured at 1973. For this reason the plutonium ecologycal path has been from Palomares sorroundings into the sea. Sites in the Mediterranean sea not affected by plutonium apportation from Almanzora river showed Pu levels approximately the same as the mean value for the whole

The distribution of plutonium-239 and americium-241 in the Syrian hamster following its intravenous administration as citrate

International Nuclear Information System (INIS)

Rodwell, P.; Stather, J.W.

1978-01-01

Actinide distribution in various tissues and the skeleton of hamsters by liquid scintillation counting or isotope dilution. For plutonium 57% of activity was concentrated in the skeleton and more than 90% in the liver and skeleton after seven days. For americium the liver retained more than 50% of total activity and 25% was excreted in urine within seven days. (U.K.)

Distribution of radium and plutonium in human bone

International Nuclear Information System (INIS)

Schlenker, R.A.

1985-01-01

This review covers studies of the microdistribution of radium and plutonium in human bone, conducted at Argonne with emphasis on the alpha-spectrometric method of measurement. Alpha spectrometry offers high spatial resolution and is well suited to the measurement of radionuclide concentrations near bone surfaces. With these techniques surface deposit thicknesses have been measured to be about 1 μm thick for isotopes of lead, radium and the actinides, and volume deposits of 226 Ra have been found to be quite nonuniform near bone surfaces, leading to endosteal tissue dose rates that are higher than expected under the assumption of uniform volume concentration normally used in radiation protection calculations. With autoradiography, the bony septa of the mastoid air cell system have been found to be depleted in radium relative to the bone tissue surrounding them; this is expected to have a significant influence on the dosimetry of the mastoid epithelia. A combination of autoradiographic and morphometric measurements indicates that specific activities in the axial skeleton are higher than in the appendicular skeleton, primarily because the former has higher bone surface-to-volume ratios and higher bone surface concentrations of plutonium. 19 references, 14 figures, 6 tables

Chemical characterization of local and stratospheric plutonium in Ohio soils

International Nuclear Information System (INIS)

Muller, R.N.

1978-01-01

The chemical nature of plutonium derived from stratospheric fallout and industrial sources was studied in three agricultural soils. The majority of the soil plutonium was associated with a reductant-soluble, hydrous oxide phase that, under most conditions of terrestrial ecosystems, remains essentially immobile. The proportion of plutonium associated with organic matter (0.1N NaOH-extractable) varied among soils, and increased with decreasing particle size in the same soil. In a soil containing 238 Pu from a local fabrication facility and 239 , 240 Pu from stratospheric fallout, isotopic ratios between the NaOH-extractable and residual phases were essentially constant, indicating that, in these soils, plutonium from both sources behaves similarly. The distribution of soil plutonium with particle size appears to be most directly related to the mass of the soil particle

Studies on the behavior of plutonium(IV) in alkaline carbonate/bicarbonate media

International Nuclear Information System (INIS)

Charyulu, M.M.; Satao, K.J.; Sivaramakrishnan, C.K.; Patil, S.K.

1986-01-01

Distribution ratios of plutonium(IV) between carbonate/bicarbonate media and strong base anion exchanger Amberlyst A-26 have been measured. Distribution ratio values are much higher in case of bicarbonate medium. The equilibrium was also achieved in a very short period in this medium. These data indicate feasibility of recovery of plutonium from such aqueous media using simple ion exchange method. (author)

Sampling and Analysis Plan for the 233-S Plutonium Concentration Facility

International Nuclear Information System (INIS)

Mihalic, M.A.

1998-02-01

This Sampling and Analysis Plan (SAP) provides the information and instructions to be used for sampling and analysis activities in the 233-S Plutonium Concentration Facility. The information and instructions herein are separated into three parts and address the Data Quality Objective (DQO) Summary Report, Quality Assurance Project Plan (QAP), and SAP

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)

Development of isotope dilution gamma-ray spectrometry for plutonium analysis

Energy Technology Data Exchange (ETDEWEB)

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

1991-01-01

We are studying the feasibility of determining the plutonium concentration and isotopic distribution of highly radioactive, spent-fuel dissolver solutions by employing high-resolution gamma-ray spectrometry. The study involves gamma-ray plutonium isotopic analysis for both dissolver and spiked dissolver solution samples, after plutonium is eluted through an ion-exchange column and absorbed in a small resin bead bag. The spike is well characterized, dry plutonium containing {approximately}98% of {sup 239}Pu. By using measured isotopic information, the concentration of elemental plutonium in the dissolver solution can be determined. Both the plutonium concentration and the isotopic composition of the dissolver solution obtained from this study agree well with values obtained by traditional isotope dilution mass spectrometry (IDMS). Because it is rapid, easy to operate and maintain, and costs less, this new technique could be an alternative method to IDMS for input accountability and verification measurements in reprocessing plants. 7 refs., 4 figs., 4 tabs.

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)

Dresden 1 Plutonium Recycle Program report, January 1, 1976--June 30, 1976

International Nuclear Information System (INIS)

Wan, M.Y.

1977-01-01

This report on the Dresden 1 Plutonium Recycle Demonstration Program covers the period from January 1, 1976 through June 30, 1976. Included are a summary of reactor operations, power and exposure histories for each mixed-oxide assembly, and the plans and schedule for the remainder of the program

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

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.)

Plutonium Round Robin Test

International Nuclear Information System (INIS)

Dudder, G.B.; Herbillon, G.H.

2001-01-01

Full text: The goal of nuclear forensics is to develop a preferred approach to illicit trafficking investigations. This approach must be widely understood and acceptable as credible. The principle objectives of the Round Robin Test are to prioritize the forensic techniques and methods, evaluate attribution capabilities, and examine the utility of database. The Plutonium Round Robin has made a tremendous contribution to fulfilling these goals through a collaborative learning experience that resulted from the outstanding efforts of the six participating international laboratories. A prioritize list of techniques and methods has been developed based on this exercise. Future work will focus on a Highly Enriched Round Robin and extent to which the techniques and methods can be generalized. The Plutonium Round Robin demonstrated a rather high level of capability to determine the important characteristics of the materials and processes using analytical methods. When this capability to was combined with the appropriate knowledge and database, it resulted in a demonstrated capability to attribute the source of the materials to a specific nuclear fuel, reactor, and reprocessing facility. A number of shortfalls were also identified in our current capabilities. These included alternative dating techniques. Light Water Reactor discrimination techniques, and the lack of a comprehensive network of data/knowledge bases. The result of the Round Robin will be used to develop guidelines or a 'recommended protocol' to be made available to the interested authorities and countries to use in real cases. The poster will present a summary of the results of the Plutonium Round Robin and describe the plans the subsequent Highly Enriched Uranium Round Robin Test. (author)

Radioecology of natural systems. Three year summary report, May 1, 1974--July 31, 1977

International Nuclear Information System (INIS)

Whicker, F.W.

1977-01-01

This report is intended to provide a general summary of the progress and findings of studies during the period May 1, 1974 through July 31, 1977 on the distribution, transport, characterization and ecological consequences of plutonium in the terrestrial environs of the Rocky Flats nuclear weapons plant near Denver, Colorado. The contamination of a portion of the terrestrial environs of Rocky Flats with substantial quantities of plutonium provided the opportunity to search for possible ecological effects resulting from the presence of the element. Comparisons were made of various biological measurements and pathological data between ecologically similar study areas of widely varying plutonium levels. Soil in the principal study areas ranged from 100 to over 20,000 dpm 239 Pu/g in the upper 3 cm (2 to 400 μCi/m 2 ). In addition, comparative data were obtained from control areas, containing only world-wide fallout plutonium of the order of 0.1 dpm/g (0.002 μCi/m 2 ). Biological measurements such as vegetation community structure and biomass; litter mass; arthropod community structure and biomass; and small mammal species occurrence, population density, biomass, reproduction, and physical size of whole carcass and organs were made. In addition, pathological examinations of small mammals, including x-ray for skeletal sarcomas, microscopy for lung tumors, and necropsy for general pathology and parasite occurrence were carried out. While minor differences in certain biological attributes between study areas were observed, none could be related to plutonium levels

Comments on a paper entitled: Toxicity and carcinogenicity of plutonium-239

International Nuclear Information System (INIS)

Stocum, W.E.; Pigg, C.J.

1978-06-01

Studies on carcinogenic effects of Pu-239 on animals have been reviewed often in the literature. A summary of these studies, which were done primarily with dogs or rats, shows that the inhalation of Pu-239 results in plutonium being retained in highest concentrations in bone, liver, lung, and lymph nodes. This may result in the induction of specific kinds of cancer, primarily lung and bone carcinomas, and to a lesser extent, bile duct tumors. These animal studies have been extremely useful in the analysis of the limited number of studies available on humans exposed to plutonium and in the prediction of plutonium cancer risk to man. One of the most significant and relevant studies on human exposures to Pu-239 is that of the 1944-45 exposure at Los Alamos Scientific Laboratory. Twenty-five men associated with the Manhattan Project were identified as having had significant plutonium exposures; total initial lung burden across the group was approximately 10 μCi. These individuals have been monitored clinically and in laboratory studies for the past 30 years. None of the individuals has shown cancer incidence and none shows medical findings attributable to internally deposited plutonium. There has been no recorded instance of cancer in man resulting from the internal deposition of any plutonium isotope in the more than three decades in which plutonium has been used. This excellent record illustrates the effectiveness of control measures and safety standards imposed on the handling of radioactive materials. These facts lead to a high level of confidence that the transportation of radioactive materials to and around the WIPP would not have a markedly different record

Plutonium in intertidal coastal and estuarine sediments in the Northern Irish Sea

International Nuclear Information System (INIS)

Aston, S.R.; Assinder, D.J.; Kelly, M.

1985-01-01

Surface intertidal sediments from 35 sites in the Irish Sea have been analysed for their 238 Pu and sup(239,240)Pu activities, together with an intensive study of plutonium in sediments of the Esk Estuary (NW England). The range of plutonium activities for the whole survey were 0.14-4118 and 1.3-16 026 Bq kg -1 for 238 Pu and sup(239,240)Pu, respectively. The levels of Pu activity, derived from the Sellafield nuclear fuel reprocessing effluents, in sediments are controlled by lithological factors and the influence of transport and post-depositional processes. Grain size distribution is particularly important, the major part of plutonium activity being in the mud fraction of all sediments. The data suggest that over the Irish Sea coastline, dynamic mixing of sediment grains by reworking and resuspension and/or by dispersion in tidal currents are important in determining plutonium distributions. The exponential decrease in sediment plutonium activities away from the Sellafield source is attributed to the progressive mixing with older contaminated and uncontaminated sediments. (author)

Electron hybridization effects and the crystal structure of plutonium: Progress report, January 1, 1987--May 31, 1988

International Nuclear Information System (INIS)

Cooper, B.R.

1988-01-01

The main research effort during the past year was on the theory of surface electronic behavior of plutonium. This research was described in last year's Progress Report and deals with both development of the resonant band-f scattering theory for the magnetic properties of highly correlated actinide systems and the synthesis of band and model Hamiltonian theory for actinide systems. A summary of the results for the surface electronic behavior of plutonium are included

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.)

Programme of research and development on plutonium recycling in light-water reactors; indirect nuclear action

International Nuclear Information System (INIS)

1982-01-01

This report is a summary of the results obtained during the five-year programme 'Plutonium recycle in LWRs' (1975-79) which has been made possible after the completion of the synthesis studies on 'Control and Safety' and on the 'Environmental impact'. The work performed during the programme is reported; the contracts concluded and their main results and conclusions are summarized. The activity was devoted to studies of general interest and to R and D in order to improve the scientific and technical knowledge of plutonium recycling. General studies included an assessment of the environmental impact of plutonium recycling in the EC as well as research aimed at reducing this impact. Improvements were achieved on neutron-physics parameters of the actinides, on neutron computer codes for plutonium-fuelled LWRs, on control and safety and on the in-pile behaviour of mixed-oxide fuels. The conclusions state that, while fostering a fruitful exchange of information in the Community, the programme has contributed to demonstrating the feasibility of plutonium recycling in LWRs

Plutonium in the Arctic Marine Environment — A Short Review

Directory of Open Access Journals (Sweden)

Lindis Skipperud

2004-01-01

Full Text Available Anthropogenic plutonium has been introduced into the environment over the past 50 years as the result of the detonation of nuclear weapons and operational releases from the nuclear industry. In the Arctic environment, the main source of plutonium is from atmospheric weapons testing, which has resulted in a relatively uniform, underlying global distribution of plutonium. Previous studies of plutonium in the Kara Sea have shown that, at certain sites, other releases have given rise to enhanced local concentrations. Since different plutonium sources are characterised by distinctive plutonium-isotope ratios, evidence of a localised influence can be supported by clear perturbations in the plutonium-isotope ratio fingerprints as compared to the known ratio in global fallout. In Kara Sea sites, such perturbations have been observed as a result of underwater weapons tests at Chernaya Bay, dumped radioactive waste in Novaya Zemlya, and terrestrial runoff from the Ob and Yenisey Rivers. Measurement of the plutonium-isotope ratios offers both a means of identifying the origin of radionuclide contamination and the influence of the various nuclear installations on inputs to the Arctic, as well as a potential method for following the movement of water and sediment loads in the rivers.

Plutonium chemistry of the ocean

International Nuclear Information System (INIS)

Folsom, T.R.

1972-01-01

Plutonium is a man-made element whose behavior in the marine environment is inadequately known at present. It has been studied intensively in connection with production of weapons and power sources and has been characterized as an extremely toxic substance. Nevertheless, only a few dozen measurements have been made of concentrations in seawater and in the associated organisms and sediments. The first of these were as recent as 1964. There are reasons to believe its chemical behavior in the ocean is different from what has been observed on land, and that it will be difficult to predict how plutonium will distribute itself in the ocean. The consequences of increased environmental concentrations of Pu are discussed

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

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

Environmental behaviour of plutonium accidentally released at Thule, Greenland

International Nuclear Information System (INIS)

Aarkrog, A.

1977-01-01

The environmental contamination resulting from the B-52 accident in 1968 at Thule was studied by scientific expeditions in 1968, 1970 and 1974. The contamination was mainly confined to the marine environment, where plutonium was preferentially located in the sediments and the benthic fauna. Plutonium concentrations down through the sediment layers decayed exponentially with a half-depth of 1 to 2 cm. The horizontal distribution of the plutonium may be described by an exponential expression: mCi sup(239,240)Pu km -2 = 460sub(e)sup(-0.28R) or by a power function: mCisup(239,240)Pu km -2 = 370 Rsup(-1.2), where R is the distance in km from the point of impact. The inventory of sup(239,240)Pu in the marine environment from the accident was estimated at 25 to 30 Ci. The amount of 238 Pu was approximately 0.5 Ci. The bottom animals, such as worms and molluscs, showed a horizontal distribution of radioactivity similar to that of the sediments. From 1968 to 1970 the sup(239,240)Pu concentrations in the biota decreased by an order of magnitude, since 1970 the decrease has been less evident. In 1970 and 1974 there were no indications of increased plutonium concentrations in surface seawater or in sea plants or zooplankton. Higher animals such as fish, seabirds and marine mammals have shown no tendency to increasing plutonium levels since the accident. (author)

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

Radial plutonium redistribution in mixed-oxide fuel

International Nuclear Information System (INIS)

Lawrence, L.A.; Schwinkendorf, K.N.; Karnesky, R.A.

1981-10-01

Alpha autoradiographs from all HEDL fuel pin metallography samples are evaluated and catalogued according to different plutonium distribution patterns. The data base is analyzed for effects of fabrication and operating parameters on redistribution

Plutonium cores of zenith

Energy Technology Data Exchange (ETDEWEB)

Barclay, F R; Cameron, I R; Drageset, A; Freemantle, R G; Wilson, D J

1965-03-15

The report describes a series of experiments carried out with plutonium fuel in the heated zero power reactor ZENITH, with the aim of testing current theoretical methods, with particular reference to excess reactivity, temperature coefficients, differential spectrum and reaction rate distributions. Two cores of widely different fissile/moderator atom ratios were loaded in order to test the theory under significantly varied spectrum conditions.

Reactor-Based Plutonium Disposition: Opportunities, Options, and Issues

International Nuclear Information System (INIS)

Greene, S.R.

1999-01-01

The end of the Cold War has created a legacy of surplus fissile materials (plutonium and highly enriched uranium) in the United States (U.S.) and the former Soviet Union. These materials pose a danger to national and international security. During the past few years, the U.S. and Russia have engaged in an ongoing dialog concerning the safe storage and disposition of surplus fissile material stockpiles. In January 1997, the Department of Energy (DOE) announced the U. S. would pursue a dual track approach to rendering approximately 50 metric tons of plutonium inaccessible for use in nuclear weapons. One track involves immobilizing the plutonium by combining it with high-level radioactive waste in glass or ceramic ''logs''. The other method, referred to as reactor-based disposition, converts plutonium into mixed oxide (MOX) fuel for nuclear reactors. The U.S. and Russia are moving ahead rapidly to develop and demonstrate the technology required to implement the MOX option in their respective countries. U.S. MOX fuel research and development activities were started in the 1950s, with irradiation of MOX fuel rods in commercial light water reactors (LWR) from the 1960s--1980s. In all, a few thousand MOX fuel rods were successfully irradiated. Though much of this work was performed with weapons-grade or ''near'' weapons-grade plutonium--and favorable fuel performance was observed--the applicability of this data for licensing and use of weapons-grade MOX fuel manufactured with modern fuel fabrication processes is somewhat limited. The U.S. and Russia are currently engaged in an intensive research, development, and demonstration program to support implementation of the MOX option in our two countries. This paper focuses on work performed in the U.S. and provides a brief summary of joint U.S./Russian work currently underway

Reactor-based plutonium disposition: Opportunities, options, and issues

International Nuclear Information System (INIS)

Greene, S.

2000-01-01

The end of the Cold War has created a legacy of surplus fissile materials (plutonium and highly enriched uranium) in the United States (U.S.) and the former Soviet Union. These materials pose a danger to national and international security. During the past few years, the U.S. and Russia have engaged in an ongoing dialog concerning the safe storage and disposition of surplus fissile material stockpiles. In January 1997, the Department of Energy (DOE) announced the U.S. would pursue a dual track approach to rendering approximately 50 metric tons of plutonium inaccessible for use in nuclear weapons. One track involves immobilizing the plutonium by combining it with high-level radioactive waste in glass or ceramic ''logs''. The other method, referred to as reactor-based disposition, converts plutonium into mixed oxide (MOX) fuel for nuclear reactors. The U.S. and Russia are moving ahead rapidly to develop and demonstrate the technology required to implement the MOX option in their respective countries. U.S. MOX fuel research and development activities were started in the 1950s with irradiation of MOX fuel rods in commercial light water reactors (LWR) from the 1960s-1980s. In all, a few thousand MOX fuel rods were successfully irradiated. Though much of this work was performed with weapons-grade or ''near'' weapons-grade plutonium - and favorable fuel performance was observed - the applicability of this data for licensing and use of weapons-grade MOX fuel manufactured with modem fuel fabrication processes is somewhat limited. The U.S. and Russia are currently engaged in an intensive research, development, and demonstration program to support implementation of the MOX option in our two countries. This paper focuses on work performed in the U.S. and provides a brief summary of joint U.S./Russian work currently underway. (author)

Post-depositional reactivity of the plutonium in different sediment facies from the English channel - an experimental approach

International Nuclear Information System (INIS)

Gouzy, A.; Boust, D.; Klein, A.

2004-01-01

The plutonium discharged into sea (in particular resulting from the activity of the reprocessing plants of nuclear fuels) presents a great affinity for the sedimentary particles. In the English Channel, the weakness of the plutonium concentrations met in the natural environment makes very difficult a direct study of the diagenetic phenomena which influences on the behavior of this radionuclide after its incorporation to the sedimentary column. On the scale of the all English Channel, the stock of plutonium immobilized in the sediments is significant (some TBq), this fact justifies the study of its becoming. With this intention, we constructed a set of experiments on series marine sediments with various sedimentological facies, which have been spiked with plutonium. After a one-month incubation period, various parameters describing the behavior of plutonium were given: (1) distribution of plutonium between the particulate phases and the pore waters; (2) quantification of plutonium associated with reactive sulphides; (3) distribution of plutonium between the particles and the seawater during a sediment resuspension episode. (author)

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)

Seismic safety of the LLL plutonium facility (Building 332)

International Nuclear Information System (INIS)

Torkarz, F.J.; Shaw, G.

1980-01-01

This report states the basis for the Lawrence Livermore Laboratory's assurance to the public that the plutonium operations at the Laboratory pose essentially no risk to anyone's health or safety, either under normal circumstances or in the event of an earthquake or a fire. The report is intended for a general audience, and so for the most part it is not highly technical. It summarizes the steps taken to ensure the seismic safety of the plutonium facility (Bldg. 332). It describes plutonium and its potential hazard and how the facility copes with that hazard. It recounts the geologic investigations and interpretations that led to the design-basis earthquake (DBE) for the Livermore site, and presents a summary analysis of the facility structure in relation to the DBE. An appendix presents a quantitative calculation of the health risk to the public associated with the worst-case hypothetical fire. The document supports the conclusions that the facility will continue to function safely after the maximum earthquake ground motion to which it may be subjected and that there is no evidence of a potential for surface offset under it

Survey of Worldwide Light Water Reactor Experience with Mixed Uranium-Plutonium Oxide Fuel

Energy Technology Data Exchange (ETDEWEB)

Cowell, B.S.; Fisher, S.E.

1999-02-01

The US and the Former Soviet Union (FSU) have recently declared quantities of weapons materials, including weapons-grade (WG) plutonium, excess to strategic requirements. One of the leading candidates for the disposition of excess WG plutonium is irradiation in light water reactors (LWRs) as mixed uranium-plutonium oxide (MOX) fuel. A description of the MOX fuel fabrication techniques in worldwide use is presented. A comprehensive examination of the domestic MOX experience in US reactors obtained during the 1960s, 1970s, and early 1980s is also presented. This experience is described by manufacturer and is also categorized by the reactor facility that irradiated the MOX fuel. A limited summary of the international experience with MOX fuels is also presented. A review of MOX fuel and its performance is conducted in view of the special considerations associated with the disposition of WG plutonium. Based on the available information, it appears that adoption of foreign commercial MOX technology from one of the successful MOX fuel vendors will minimize the technical risks to the overall mission. The conclusion is made that the existing MOX fuel experience base suggests that disposition of excess weapons plutonium through irradiation in LWRs is a technically attractive option.

Survey of Worldwide Light Water Reactor Experience with Mixed Uranium-Plutonium Oxide Fuel

International Nuclear Information System (INIS)

Cowell, B.S.; Fisher, S.E.

1999-01-01

The US and the Former Soviet Union (FSU) have recently declared quantities of weapons materials, including weapons-grade (WG) plutonium, excess to strategic requirements. One of the leading candidates for the disposition of excess WG plutonium is irradiation in light water reactors (LWRs) as mixed uranium-plutonium oxide (MOX) fuel. A description of the MOX fuel fabrication techniques in worldwide use is presented. A comprehensive examination of the domestic MOX experience in US reactors obtained during the 1960s, 1970s, and early 1980s is also presented. This experience is described by manufacturer and is also categorized by the reactor facility that irradiated the MOX fuel. A limited summary of the international experience with MOX fuels is also presented. A review of MOX fuel and its performance is conducted in view of the special considerations associated with the disposition of WG plutonium. Based on the available information, it appears that adoption of foreign commercial MOX technology from one of the successful MOX fuel vendors will minimize the technical risks to the overall mission. The conclusion is made that the existing MOX fuel experience base suggests that disposition of excess weapons plutonium through irradiation in LWRs is a technically attractive option

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

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)

Occurrence of plutonium in the terrestrial environment at Thule, Greenland

DEFF Research Database (Denmark)

Roos, Per; Jernström, Jussi; Nielsen, Sven Poul

2011-01-01

Samples of air, resuspended particles, water, soil and precipitation were collected in an area 10 km south of the Thule 1968 impact point and analysed for their content of 241Am and plutonium. The results from the soil sampling show a very inhomogeneous distribution with hot spots ranging up...... to several hundred kBq per m2 of Pu. Although concentrations in surface soil can be very high the concentration in analysed air filter samples and passive aerosol collectors are very low. Exposure to plutonium due to inhalation of airborne plutonium particles in the area is of little importance according...

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.)

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.

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

Surplus plutonium disposition draft environmental impact statement. Volume 1, Part B

International Nuclear Information System (INIS)

1998-07-01

On May 22, 1997, DOE published a Notice of Intent (NOI) in the Federal Register (62 Federal Register 28009) announcing its decision to prepare an environmental impact statement (EIS) that would tier from the analysis and decisions reached in connection with the Storage and Disposition of Weapons-Usable Fissile Materials Final Programmatic EIS (Storage and Disposition PEIS). DOE's disposition strategy allows for both the immobilization of surplus plutonium and its use as mixed oxide (MOX) fuel in existing domestic, commercial reactors. The disposition of surplus plutonium would also involve disposal of the immobilized plutonium and MOX fuel (as spent nuclear fuel) in a geologic repository. The Surplus Plutonium Disposition Environmental Impact Statement analyzes alternatives that would use the immobilization approach (for some of the surplus plutonium) and the MOX fuel approach (for some of the surplus plutonium); alternatives that would immobilize all of the surplus plutonium; and the No Action Alternative. The alternatives include three disposition facilities that would be designed so that they could collectively accomplish disposition of up to 50 metric tons (55 tons) of surplus plutonium over their operating lives: (1) the pit disassembly and conversion facility would disassemble pits (a weapons component) and convert the recovered plutonium, as well as plutonium metal from other sources, into plutonium dioxide suitable for disposition; (2) the immobilization facility would include a collocated capability for converting nonpit plutonium materials into plutonium dioxide suitable for immobilization and would be located at either Hanford or SRS. DOE has identified SRS as the preferred site for an immobilization facility; (3) the MOX fuel fabrication facility would fabricate plutonium dioxide into MOX fuel. This volume has chapters on environmental consequences; environmental regulations, permits, and consultations; a glossary; list of preparers; distribution list

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

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

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.

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

Plutonium in Atlantic coastal estuaries in the southeastern United States of America

International Nuclear Information System (INIS)

Hayes, D.W.; LeRoy, J.H.; Cross, F.A.

1976-01-01

A survey was made to begin to provide baseline information on the plutonium distribution of representative estuarine and coastal areas of the southeastern United States of America. Sediments and marsh grass (Spartina) were collected and analysed from three locations within a tidal marsh. In the three estuaries (Savannah, Neuse and Newport) the suspended particulate matter (1μm and greater) was filtered from waters with different salinities and the plutonium content of the particulates determined. The Savannah river estuary, in addition to fall-out plutonium, has received up to 0.3Ci of plutonium from the Savannah River Plant (SRP) of the US Energy Research and Development Administration. The SRP plutonium has a variable isotopic composition that can influence plutonium isotopic ratios in the estuarine system. The other estuaries do not have nuclear installations upstream. Plutonium contents in surface marsh sediment from the Savannah River estuary are lower than those found in nearby bay sediments. In fact, total plutonium concentrations of sediments showed increases from the upper to lower portions of the estuary; however, higher contributions of 238 Pu in the upper portions indicate that releases from the Savannah River Plant do contribute plutonium to the Savannah river estuary. Plutonium concentrations in Spartina were less than 10fCi/g dry weight but are higher than plutonium contents of terrestrial plants ( 238 Pu to the total plutonium activities in the sediment and the Spartina. Plutonium concentrations were about three times higher in the Newport river estuary than in the Neuse and Savannah river estuaries. (author)

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.)

Livermore Big Trees Park: 1998 summary results; TOPICAL

International Nuclear Information System (INIS)

Gallegos, G; MacQueen, D; Surano, K

1999-01-01

This report summarizes work conducted in 1998 by the Lawrence Livermore National Laboratory (LLNL) to determine the extent and origin of plutonium at concentrations above background levels at Big Trees Park in the city of Livermore. This summary includes the project background and sections that explain the sampling, radiochemical and data analysis, and data interpretation. This report is a summary report only and is not intended as a rigorous technical or statistical analysis of the data

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)

Preliminary studies on the spatial-temporal microdistribution of inhaled soluble plutonium in the lungs of dogs

International Nuclear Information System (INIS)

Cho, M.W.; Dagle, G.E.

1987-01-01

The pulmonary microdistribution of inhaled soluble plutonium in four beagle dogs was studied in autoradiographs of histologic sections and transmission electron micrographs of lungs. Dogs were exposed to a single nose-only aerosol of 239 Pu nitrate with a post-exposure time ranging from 1 month to 42 months. At one month after the exposure, the plutonium was dispersed throughout the lung section, with a higher percentage of the activity found on alveolar macrophages and alveolar septa. However, a nonrandom localization of the plutonium was observed as time passed. The focal concentrations were primarily in nodular or diffuse interstitial fibrotic tissues typically contiguous with subpleural, peribronchial, or perivascular areas. More than 50% of the total activity was in the form of single-tracks at one month exposure, and this percentage increased with time. In summary, this preliminary study suggests an initial random dispersion of soluble plutonium with increased concentration of activity to nonrandom focal locations with time

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)

Influence of the Cr2O3 sintering additive on the homogenization of the plutonium distribution inside an heterogeneous MOX pellet

International Nuclear Information System (INIS)

Pieragnoli, A.

2007-12-01

This work has revealed the nature of the Cr 2 O 3 action mechanisms on the development of the microstructure of a MOX pellet and particularly on the improvement of the plutonium distribution. At first, it has been necessary to study thoroughly the description of the interaction phenomena occurring inside the U-Pu-Cr-O system. A model system constituted by the same materials UO 2 , (U, Pu)O 2 and Cr 2 O 3 than those present in a MOX pellet and thermically heated in similar sintering conditions has been carried out. These tests have been completed by studies concerning the reactivity between PuO 2 and Cr 2 O 3 , the interdiffusion between UO 2 and (U, Pu)O 2 in presence of chromium and the solubility of chromium in (U, Pu)O 2 . Then, with all the data acquired, it has been possible to describe the evolution of a MOX pellet in presence of chromium during the sintering of the microstructure. Microstructural characteristics such as the plutonium homogenization degree and the grain size have been studied with temperature and sintering level period. The chromium oxide inside microstructure has been studied too. At last, an interpretation of the influence of the presence of chromium on the development of a MOX pellet microstructure has been given in focusing particularly on the plutonium distribution. This interpretation is based on the formation of the (U, Pu)CrO 3 phase and on the plutonium oxidation degree stabilization (+III) by chromium at the grain boundaries level. Advices aiming at optimizing the chromium impact on the development of microstructure are given. In most of the cases, these advices are based on solutions which will contribute, during the sintering thermal treatment, to the presence at lower temperature of the (U, Pu)CrO 3 phase and to keep longer a greater quantity of chromium inside the MOX pellet. (O.M.)

Reference computations of public dose and cancer risk from airborne releases of uranium and Class W plutonium

International Nuclear Information System (INIS)

Peterson, V.L.

1995-01-01

This report presents ''reference'' computations that can be used by safety analysts in the evaluations of the consequences of postulated atmospheric releases of radionuclides from the Rocky Flats Environmental Technology Site. These computations deal specifically with doses and health risks to the public. The radionuclides considered are Class W Plutonium, all classes of Enriched Uranium, and all classes of Depleted Uranium. (The other class of plutonium, Y, was treated in an earlier report.) In each case, one gram of the respirable material is assumed to be released at ground leveL both with and without fire. The resulting doses and health risks can be scaled to whatever amount of release is appropriate for a postulated accident being investigated. The report begins with a summary of the organ-specific stochastic risk factors appropriate for alpha radiation, which poses the main health risk of plutonium and uranium. This is followed by a summary of the atmospheric dispersion factors for unfavorable and typical weather conditions for the calculation of consequences to both the Maximum Offsite Individual and the general population within 80 km (50 miles) of the site

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)

Complexation of Plutonium (IV) With Sulfate At Variable Temperatures

International Nuclear Information System (INIS)

Y. Xia; J.I. Friese; D.A. Moore; P.P. Bachelor; L. Rao

2006-01-01

The complexation of plutonium(IV) with sulfate at variable temperatures has been investigated by solvent extraction method. A NaBrO 3 solution was used as holding oxidant to maintain the plutonium(IV) oxidation state throughout the experiments. The distribution ratio of Pu(IV) between the organic and aqueous phases was found to decrease as the concentrations of sulfate were increased. Stability constants of the 1:1 and 1:2 Pu(IV)-HSO 4 - complexes, dominant in the aqueous phase, were calculated from the effect of [HSO 4 - ] on the distribution ratio. The enthalpy and entropy of complexation were calculated from the stability constants at different temperatures using the Van't Hoff equation

Fused salt processing of impure plutonium dioxide to high-purity plutonium metal

International Nuclear Information System (INIS)

Mullins, L.J.; Christensen, D.C.; Babcock, B.R.

1982-01-01

A process for converting impure plutonium dioxide (approx. 96% pure) to high-purity plutonium metal (>99.9%) was developed. The process consists of reducing the oxide to an impure plutonium metal intermediate with calcium metal in molten calcium chloride. The impure intermediate metal is cast into an anode and electrorefined to produce high-purity plutonium metal. The oxide reduction step is being done now on a 0.6-kg scale with the resulting yield being >99.5%. The electrorefining is being done on a 4.0-kg scale with the resulting yield being 80 to 85%. The purity of the product, which averages 99.98%, is essentially insensitive to the purity of the feed metal. The yield, however, is directly dependent on the chemical composition of the feed. To date, approximately 250 kg of impure oxide has been converted to pure metal by this processing sequence. The availability of impure plutonium dioxide, together with the need for pure plutonium metal, makes this sequence a valuable plutonium processing tool

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...

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.

Optimization and implementation study of plutonium disposition using existing CANDU Reactors. Final report

International Nuclear Information System (INIS)

1996-09-01

Since early 1994, the Department of Energy has been sponsoring studies aimed at evaluating the merits of disposing of surplus US weapons plutonium as Mixed Oxide (MOX) fuel in existing commercial Canadian Pressurized Heavy Water reactors, known as CANDU's. The first report, submitted to DOE in July, 1994 (the 1994 Executive Summary is attached), identified practical and safe options for the consumption of 50 to 100 tons of plutonium in 25 years in some of the existing CANDU reactors operating the Bruce A generating station, on Lake Huron, about 300 km north east of Detroit. By designing the fuel and nuclear performance to operate within existing experience and operating/performance envelope, and by utilizing existing fuel fabrication and transportation facilities and methods, a low cost, low risk method for long term plutonium disposition was developed. In December, 1995, in response to evolving Mission Requirements, the DOE requested a further study of the CANDU option with emphasis on more rapid disposition of the plutonium, and retaining the early start and low risk features of the earlier work. This report is the result of that additional work

Retention of plutonium in the beagle after gastrointestinal absorption

International Nuclear Information System (INIS)

Toohey, R.E.; Bhattacharyya, M.H.; Oldham, R.D.; Larsen, R.P.; Moretti, E.S.

1985-01-01

A 0.01 M bicarbonate solution containing 130 nCi (approx. 5 kBq) of 237 Pu (90% hexavalent, 93% ultrafilterable) was administered via gelatin capsule to six adult male beagles following a 21-hr fast. The dogs were sacrificed after 5-6 weeks and the percentage of the administered plutonium retained in the liver plus skeleton and its distribution within the skeleton were determined. The mean amount retained in these tissues was (0.063 +- 0.006)% of the administered dose. The mean amounts of plutonium in the liver and the skeleton were approximately equal, and the distribution within the skeleton was similar to that observed by other workers following either intravenous injection or inhalation. The value for plutonium retention by the dog is about a factor of three less than the values the authors have reported for rodents. It is a factor of 7 greater than the product of the values for gastrointestinal absorption (f 1 ) and fractional retention (f 2 ) recommended by the ICRP for man

The separation of plutonium from uranium and fission products on zirconium phosphate columns

Energy Technology Data Exchange (ETDEWEB)

Gal, I; Ruvarac, A [Institute of Nuclear Sciences Boris Kidric, Laboratorija za visoku aktivnost, Vinca, Beograd (Serbia and Montenegro)

1963-12-15

In recent years special attention has been given to the ion-exchange properties of zirconium phosphate and similar compounds in aqueous solutions. These inorganic cation exchangers are stable in oxidizing media and at elevated temperatures. Their resistance to ionizing radiation makes them particularly suitable for work with radioactive solutions. On account of this we considered ir worthwhile to investigate the separation of plutonium from uranium and fission products on zirconium phosphate columns. We were interested in nitric and solutions containing macro-amounts of uranium (a few grams per litre), and micro-amounts of plutonium and long-lived fission products. To obtain a better insight into the ion-exchange behaviour of the different ionic species towards zirconium phosphate, we first determined the dependence of the distribution coefficients of uranium, plutonium and fission product cations on the aqueous nitric acid concentration. Then, taking the distribution data as a guide, we separated plutonium on small glass columns filled with zirconium phosphate and calculated the decontamination factors (author)

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.

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.)

Plutonium bioassay by inductively coupled plasma mass spectrometry ICP/MS

International Nuclear Information System (INIS)

Wyse, E.J.; Fisher, D.R.

1993-04-01

The determination of plutonium in urine poses several analytical challenges, e.g., detectability, matrix, etc. We have investigated the feasibility of analyzing plutonium in processed urine by inductively coupled plasma mass spectrometry (ICP/MS). The urine samples are first spiked with 244 Pu as a tracer and internal standard, then processed by co-precipitation and column chromatography using TRU-Spec trademark, an extraction resin. By enhancing ICP/MS detection capabilities via improved sample introduction and data acquisition efficiencies, an instrumental detection limit of 5 to 50 fg (0.3 to 3 fCi for 239 pu) is typically obtained, depending on the desired degree of quantitation. A brief summary of the analytical method as well as the basis for measuring radionuclides by ICP/MS are submitted; the separation procedure, methods of sample introduction, and data acquisition techniques are then highlighted

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.)

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)

Study of plutonium-addition systems

International Nuclear Information System (INIS)

Kuchar, L.; Wozniakova, B.

1976-11-01

Steady state phase diagrams and calculated values of concentrations on the solid and liquid curves, the steady state distribution coefficient and thermodynamic control are presented for temperatures ranging from the eutectic reaction temperatures to the Pu melting point temperature for binary systems plutonium-addition (Mg, Al, Si, Ti, Mn, Fe, Co, Ni, Cu, Zn, Ga, Zr, Ru, Os, Th, U, Np). (J.P.)

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.

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

Weapons-grade plutonium dispositioning. Volume 2: Comparison of plutonium disposition options

International Nuclear Information System (INIS)

Brownson, D.A.; Hanson, D.J.; Blackman, H.S.

1993-06-01

The Secretary of Energy requested the National Academy of Sciences (NAS) Committee on International Security and Arms Control to evaluate disposition options for weapons-grade plutonium. The Idaho National Engineering Laboratory (INEL) offered to assist the NAS in this evaluation by investigating the technical aspects of the disposition options and their capability for achieving plutonium annihilation levels greater than 90%. This report was prepared for the NAS to document the gathered information and results from the requested option evaluations. Evaluations were performed for 12 plutonium disposition options involving five reactor and one accelerator-based systems. Each option was evaluated in four technical areas: (1) fuel status, (2) reactor or accelerator-based system status, (3) waste-processing status, and (4) waste disposal status. Based on these evaluations, each concept was rated on its operational capability and time to deployment. A third rating category of option costs could not be performed because of the unavailability of adequate information from the concept sponsors. The four options achieving the highest rating, in alphabetical order, are the Advanced Light Water Reactor with plutonium-based ternary fuel, the Advanced Liquid Metal Reactor with plutonium-based fuel, the Advanced Liquid Metal Reactor with uranium-plutonium-based fuel, and the Modular High Temperature Gas-Cooled Reactor with plutonium-based fuel. Of these four options, the Advanced Light Water Reactor and the Modular High Temperature Gas-Cooled Reactor do not propose reprocessing of their irradiated fuel. Time constraints and lack of detailed information did not allow for any further ratings among these four options. The INEL recommends these four options be investigated further to determine the optimum reactor design for plutonium disposition

Weapons-grade plutonium dispositioning. Volume 2: Comparison of plutonium disposition options

Energy Technology Data Exchange (ETDEWEB)

Brownson, D.A.; Hanson, D.J.; Blackman, H.S. [and others

1993-06-01

The Secretary of Energy requested the National Academy of Sciences (NAS) Committee on International Security and Arms Control to evaluate disposition options for weapons-grade plutonium. The Idaho National Engineering Laboratory (INEL) offered to assist the NAS in this evaluation by investigating the technical aspects of the disposition options and their capability for achieving plutonium annihilation levels greater than 90%. This report was prepared for the NAS to document the gathered information and results from the requested option evaluations. Evaluations were performed for 12 plutonium disposition options involving five reactor and one accelerator-based systems. Each option was evaluated in four technical areas: (1) fuel status, (2) reactor or accelerator-based system status, (3) waste-processing status, and (4) waste disposal status. Based on these evaluations, each concept was rated on its operational capability and time to deployment. A third rating category of option costs could not be performed because of the unavailability of adequate information from the concept sponsors. The four options achieving the highest rating, in alphabetical order, are the Advanced Light Water Reactor with plutonium-based ternary fuel, the Advanced Liquid Metal Reactor with plutonium-based fuel, the Advanced Liquid Metal Reactor with uranium-plutonium-based fuel, and the Modular High Temperature Gas-Cooled Reactor with plutonium-based fuel. Of these four options, the Advanced Light Water Reactor and the Modular High Temperature Gas-Cooled Reactor do not propose reprocessing of their irradiated fuel. Time constraints and lack of detailed information did not allow for any further ratings among these four options. The INEL recommends these four options be investigated further to determine the optimum reactor design for plutonium disposition.

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

A feasibility study for the storage of plutonium pits in non-partitioned warehouse facilities

International Nuclear Information System (INIS)

James, D.; Parameswaren, S.; Nagendran, S.

1999-02-01

It is projected that up to 20,000 plutonium pits will be stored at Pantex for up to 50 years. The proposed storage system has to meet longevity, safety and cost requirements. Thermal, mechanical, chemical, nuclear criticality and safety performance characteristics of any proposed plutonium container design need to be formally analyzed. Plutonium generates thermal energy as it decays. The generated thermal energy may cause excessive rise of temperature. For safety and other considerations, it is important that the plutonium temperature remains relatively constant and no hot spots develop. Plutonium containers should not be disassembled for routine monitoring and there are various reasons for the need to monitor the plutonium non-obtrusively. Therefore, accurate predictions of the temperature distribution within the storage container based upon external monitoring within the storage facility needs to be developed. A heat transfer analysis of the storage container is required. The heat transfer analysis, however, requires the knowledge of the temperature and velocity of the air circulating around the containers in order to determine the heat transferred to the air from the containers by convection. Therefore, a complete flow field analysis is required prior to performing the conduction analysis of each pit. The objective of this research is, therefore, to develop and validate a numerical model to predict the temperature distribution within the plutonium storage container as a function of the ambient air temperature within the warehouse

Technical considerations in decisions on plutonium use

International Nuclear Information System (INIS)

Till, C.E.

1980-01-01

Present-day reactors use uranium inefficiently. Really substantial increases in efficiency of uranium utilization require reprocessing. Reprocessing activities give rise to concern about their possible use in fission weapons acquisition. The basic properties of nuclides severely limit both the number of alternative ways that fuel utilization can be improved and the amount of the improvement that is possible from any of the alternatives. By far the greatest improvement comes from plutonium use in a fast reactor. The properties that allow this are peculiar to plutonium. There are basically only two fuel cycles that can be considered as alternatives to the plutonium-238/uranium fuel cycle. One is a uranium-233/thorium fuel cycle, a cycle that is very similar in requirements, including reprocessing, to the plutonium-238/uranium cycle. The other is continuation and refinement of the current once-through cycle. A small number of technical measures to increase proliferation-resistance have been proposed. Improvements of an institutional nature are of two types. The first are improvements in international safeguards - most importantly, nuclear materials accountancy - essentially strengthening or augmenting current IAEA procedures. The second involves agreements between nations to limit distribution of sensitive technologies and to multinationalize or internationalize sensitive elements of the fuel cycle

Chemical speciation of plutonium in the radioactive waste burial ground at the Savannah River Plant

International Nuclear Information System (INIS)

Wilhite, E.L.

1978-08-01

The plutonium chemical species in two types of samples from the Savannah River Plant burial ground for radioactive waste were identified. Samples analyzed were water and sediment from burial ground monitoring well C-17 and soil from an alpha waste burial trench. Soluble plutonium in the monitoring well was less than 12A in diameter, was cationic, and contained about 43% Pu(VI) and 25% Pu(IV). The equilibrium distribution coefficient (K /sub d/) for soluble plutonium from the well water (pH 7) to burial ground soil was about 60. Soil plutonium from the waste trench was not cation-exchanged; 78% of the soil plutonium was associated with metallic oxides in the soil. Approximately 9% of the Pu was contained in the crystalline soil matrix. Thus, about 87% of the plutonium in the soil was in a relatively immobile form. Ion-exchangeable and organic acid forms of plutonium amounted to only about 2.5% each. The bulk of the plutonium now on burial ground soils will be immobile except for movement of soil particles containing plutonium. 6 tables

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

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

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)

Integrated development and testing plan for the plutonium immobilization project

International Nuclear Information System (INIS)

Kan, T.

1998-01-01

This integrated plan for the DOE Office of Fissile Materials Disposition (MD) describes the technology development and major project activities necessary to support the deployment of the immobilization approach for disposition of surplus weapons-usable plutonium. The plan describes details of the development and testing (D and T) tasks needed to provide technical data for design and operation of a plutonium immobilization plant based on the ceramic can-in-canister technology (''Immobilization Fissile Material Disposition Program Final Immobilization Form Assessment and Recommendation'', UCRL-ID-128705, October 3, 1997). The plan also presents tasks for characterization and performance testing of the immobilization form to support a repository licensing application and to develop the basis for repository acceptance of the plutonium form. Essential elements of the plant project (design, construction, facility activation, etc.) are described, but not developed in detail, to indicate how the D and T results tie into the overall plant project. Given the importance of repository acceptance, specific activities to be conducted by the Office of Civilian Radioactive Waste Management (RW) to incorporate the plutonium form in the repository licensing application are provided in this document, together with a summary of how immobilization D and T activities provide input to the license activity. The ultimate goal of the Immobilization Project is to develop, construct, and operate facilities that will immobilize from about 18 to 50 tonnes (MT) of U.S. surplus weapons usable plutonium materials in a manner that meets the ''spent fuel'' standard (Fissile Materials Storage and Disposition Programmatic Environmental Impact Statement Record of Decision, ''Storage and Disposition Final PEIS'', issued January 14, 1997, 62 Federal Register 3014) and is acceptable for disposal in a geologic repository. In the can-in-canister technology, this is accomplished by encapsulating the

Control rod effects with plutonium recycle in a PWR

International Nuclear Information System (INIS)

Nash, G.; Muehl, G.J.; Gibson, I.H.

1979-03-01

A study has been made on a PWR loaded partly and wholly with plutonium to determine the changes in shutdown margin compared with an enriched uranium core. Lattice calculations are used to generate cell constants for core calculations. Three fuel loadings were considered, all uranium, 30% (approximately) of the assemblies plutonium in natural uranium, and all plutonium. The equilibrium fuel management schemes adopted in each case are based on the standard three cycle equal size batch scheme. Detailed calculations of power and irradiation distributions through the cycles have been carried out to provide a starting point for the control rod worth and requirement calculations. Control rod worths are reduced in a plutonium core because of the harder spectrum and higher fuel absorption cross sections. Furthermore, the control rod requirements for shutdown increase because of the increase in fuel and moderator temperature coefficients. This results in a reduction in shutdown margin. The magnitude of these changes is fully analysed in the report. The significance of these reductions depends on the detail of the safety argument but reductions of these sizes are unlikely to be acceptable. The data provided in this report could be used to give a first estimate of the plutonium loading acceptable given the safety assessment of the normal uranium core. (U.K.)

Threat to the New York City water supply - plutonium

International Nuclear Information System (INIS)

Bogen, D.C.; Krey, P.W.; Volchok, H.L.; Feldstein, J.; Calderon, G.

1988-01-01

The mayor of the City of New York received an anonymous letter on April 1st 1985 threatening to contaminate the water supply with plutonium unless all criminal charges against Mr Bernhard Goetz, the suspect in a dramatic subway shooting incident, were dismissed by April 11th 1985. The Environmental Measurements Laboratory, EML, was requested to analyse a composite, large volume (∼ 175 litres) drinking water sample collected on April 16th 1985. The concentration measured was 21 fCi/l which was a factor of 100 greater than previously observed results in the EML data base, and the mass isotopic content of the plutonium was very unusual. Additional samples were collected one to three months later at various distribution points in the water supply system. The plutonium concentrations were much lower and comparable to EML's earlier data. Mass isotopic analysis of these samples provided more reasonable compositions but with high uncertainties due to very low plutonium concentration. Due to the inability to confirm the elevated plutonium concentration value for the composite sample, it is impossible to conclude whether the threat to contaminate the New York City water supply was actually carried out or whether the sample was contaminated prior to receipt at EML. 5 refs.; 1 figure; 5 tabs

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.

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)

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

Development of techniques for measuring plutonium contents in TRU wastes by NDA methods

International Nuclear Information System (INIS)

Matsubayashi, Toshiyuki; Kuwana, Katsumi; Morita, Tomio; Izuhara, Shigeomi; Suzuki, Masahiro

1983-01-01

In order to develop a technique for measuring the amount of plutonium in plutonium-contaminated (TRU) wastes, a passive gamma method was selected from many candidate methods, and examined for the suitability by applying the method to low density wastes. A segmented gamma scanner was used for the experiment. The instrument is composed mainly of a Ge(Li) detector, multichannel analyser, data processing system, turntable and transmission radiation source of (75)Se. A sham waste was prepared by adding plutonium oxide powder as a radiation source to waste matrix in a 20-1 carton box. The sham waste was put on the turntable, and the detector was set at 50 cm distance from the center of the turntable. 414 keV gamma ray emitted from (239)Pu was utilized for the assay of plutonium in the experiment. The effects of combustible (paper) waste matrix, organic chlorinated material matrix, and the distribution of plutonium source in a box on the count rate were examined, and it was concluded that 1) about 10 mg of (239)Pu contained in both matrices should be assayed by the passive gamma method, 2) 50 mg of (239) Pu was measured at 30 % confidence level with 2000 sec measuring time, 3) the effect of distribution of plutonium in a waste was able to be reduced to a value of less than 15 % by rotating the waste on the turntable. (Yoshitake, I.)

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

Recycling of plutonium and uranium in water reactor fuel. Proceedings of a technical committee meeting

International Nuclear Information System (INIS)

1997-05-01

The Technical Committee Meeting on Recycling of Plutonium and Uranium in Water Reactor Fuel was recommended by the International Working Group on Fuel Performance and Technology (IWGFPT). Its aim was to obtain an overall picture of MOX fabrication capacity and technology, actual performance of this kind of fuel, and ways explored to dispose of the weapons grade plutonium. The subject of this meeting had been reviewed by the International Atomic Energy Agency every 5 to 6 years and for the first time the problem of weapons grade plutonium disposal was included. The papers presented provide a summary of experience on MOX fuel and ongoing research in this field in the participating countries. The meeting was hosted by British Nuclear Fuels plc, at Newby Bridge, United Kingdom, from 3 to 7 July 1995. Fifty-six participants from twelve countries or international organizations took part. Refs, figs, 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)

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...

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

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

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

Analysis of Radial Plutonium Isotope Distribution in Irradiated Test MOX Fuel Rods

Energy Technology Data Exchange (ETDEWEB)

Oh, Jae Yong; Lee, Byung Ho; Koo, Yang Hyun; Kim, Han Soo

2009-01-15

After Rod 3 and 6 (KAERI MOX) were irradiated in the Halden reactor, their post-irradiation examinations are being carried out now. In this report, PLUTON code was implemented to analyze Rod 3 and 6 (KAERI MOX). In the both rods, the ratio of a maximum burnup to an average burnup in the radial distribution was 1.3 and the contents of {sup 239}Pu tended to increase as the radial position approached the periphery of the fuel pellet. The detailed radial distribution of {sup 239}Pu and {sup 240}Pu, however, were somewhat different. To find the reason for this difference, the contents of Pu isotopes were investigated as the burnup increased. The content of {sup 239}Pu decreased with the burnup. The content of {sup 240}Pu increased with the burnup by the 20 GWd/tM but decreased over the 20 GWd/tM. The local burnup of Rod 3 is higher than that of Rod 6 due to the hole penetrated through the fuel rod. The content of {sup 239}Pu decreased more rapidly than that of {sup 240}Pu in the Rod 6 with the increased burnup. It resulted in a radial distribution of {sup 239}Pu and {sup 240}Pu similar to Rod 3. The ratio of Xe to Kr is a parameter to find where the fissions occur in the nuclear fuel. In both Rod 3 and 6, it was 18.3 in the whole fuel rod cross section, which showed that the fissions occurred in the plutonium.

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.

Documentation of acceptable knowledge for LANL Plutonium Facility transuranic waste streams

International Nuclear Information System (INIS)

Montoya, A.J.; Gruetzmacher, K.; Foxx, C.; Rogers, P.S.Z.

1998-01-01

Characterization of transuranic waste from the LANL Plutonium Facility for certification and transportation to WIPP includes the use of acceptable knowledge as specified in the WIPP Quality Assurance Program Plan. In accordance with a site-specific procedure, documentation of acceptable knowledge for retrievably stored and currently generated transuranic waste streams is in progress at LANL. A summary overview of the transuranic waste inventory is complete and documented in the Sampling Plan. This document also includes projected waste generation, facility missions, waste generation processes, flow diagrams, times, and material inputs. The second part of acceptable knowledge documentation consists of assembling more detailed acceptable knowledge information into auditable records and is expected to require several years to complete. These records for each waste stream must support final assignment of waste matrix parameters, EPA hazardous waste numbers, and radionuclide characterization. They must also include a determination whether waste streams are defense waste streams for compliance with the WIPP Land Withdrawal Act. The LANL Plutonium Facility's mission is primarily plutonium processing in basic special nuclear material (SNM) research activities to support national defense and energy programs. It currently has about 100 processes ranging from SNM recovery from residues to development of plutonium 238 heat sources for space applications. Its challenge is to characterize and certify waste streams from such diverse and dynamic operations using acceptable knowledge. This paper reports the progress on the certification of the first of these waste streams to the WIPP WAC

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

Decontamination of plutonium-contaminated surfaces

International Nuclear Information System (INIS)

Bertrand, J.; Clouet d'Orval, Ch.; Tachon, J.

1958-01-01

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) [fr

Review of criticality safety benchmark data of plutonium solution in ICSBEP handbook

International Nuclear Information System (INIS)

Yamamoto, Toshihiro; Miyoshi, Yoshinori; Okubo, Kiyoshi

2003-01-01

The criticality data of plutonium solutions published in the ICSBEP Handbook were reviewed. Criticality data for lower plutonium concentration and higher 240 Pu content, which correspond to a reprocessing process condition, are very scarce and hence the criticality data in this area are desired. While the calculated k eff 's with ENDF/B-V show the dependence of the plutonium concentration, the dependence has been corrected in JENDL-3.3 because of energy distribution of the capture cross section of 239 Pu. Based on the generalized perturbation theory, the sensitivity coefficient of k eff with respect to fission and capture cross section in plutonium solutions were obtained. In a plutonium solution with a lower concentration, cross sections in the thermal energy less than 0.1 eV have significant effects on the criticality. On the other hand, the criticality of higher concentration plutonium solutions is mostly dominated by cross sections in the energy range larger than 0.1 eV. Regarding the effect of 240 Pu on criticality, the capture cross section 240 Pu around the resonance peak near 1 eV is dominant regardless of the concentration. (author)

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

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 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

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

Prospective studies of HTR fuel cycles involving plutonium

International Nuclear Information System (INIS)

Bonin, B.; Greneche, D.; Carre, F.; Damian, F.; Doriath, J.Y.

2002-01-01

High Temperature Gas Cooled reactors (HTRs) are able to accommodate a wide variety of mixtures of fissile and fertile materials without any significant modification of the core design. This flexibility is due to an uncoupling between the parameters of cooling geometry, and the parameters which characterize neutronic optimisation (moderation ratio or heavy nuclide concentration and distribution). Among other advantageous features, an HTR core has a better neutron economy than a LWR because there is much less parasitic capture in the moderator (capture cross section of graphite is 100 times less than the one of water) and in internal structures. Moreover, thanks to the high resistance of the coated particles, HTR fuels are able to reach very high burn-ups, far beyond the possibilities offered by other fuels (except the special case of molten salt reactors). These features make HTRs especially interesting for closing the nuclear fuel cycle and stabilizing the plutonium inventory. A large number of fuel cycle studies are already available today, on 3 main categories of fuel cycles involving HTRs : i) High enriched uranium cycle, based on thorium utilization as a fertile material and HEU as a fissile material; ii) Low enriched uranium cycle, where only LEU is used (from 5% to 12%); iii) Plutonium cycle based on the utilization of plutonium only as a fissile material, with (or without) fertile materials. Plutonium consumption at high burnups in HTRs has already been tested with encouraging results under the DRAGON project and at Peach Bottom. To maximize plutonium consumption, recent core studies have also been performed on plutonium HTR cores, with special emphasis on weapon-grade plutonium consumption. In the following, we complete the picture by a core study for a HTR burning reactor-grade plutonium. Limits in burnup due to core neutronics are investigated for this type of fuel. With these limits in mind, we study in some detail the Pu cycle in the special case of a

Irradiation of the foetus from maternal intakes of plutonium

International Nuclear Information System (INIS)

Adams, N.; Stather, J.W.

1984-01-01

A brief review is given of published animal data on the initial uptake of activity by the foetal and maternal tissues following entry of plutonium into body fluids at various stages during gestation, on the extent to which activity deposited in maternal tissues is subsequently translocated to the foetus and on its distribution in the tissues of the developing foetus. The limited data available from these animal studies do not readily allow the development of a comprehensive human foetal metabolic model but they do suggest a method for estimating radiation doses to the foetus from maternal intakes of plutonium. (U.K.)

A passive gamma scanner for estimation of plutonium in fabrication waste

International Nuclear Information System (INIS)

Venkatesan, P.P.; Burte, P.P.; Manohar, S.B.; Satya Prakash; Ramaniah, M.V.

1978-01-01

The solid plutonium wastes arising from plutonium handling laboratories and fuel fabrication facilities by their very nature (heterogeneous) are not amenable to proper sampling and hence to the standard techniques of estimation. For the proper accounting of nuclear materials a non-destructive method of waste assay is essential. A passive gamma-ray scanner developed in the Radiochemistry Division is described in the present report. The scanner detects the 384 KeV gamma complex of plutonium in a (3'' x 3'') NaI(Tl) detector. The rotation-collimation technique is used to achieve the flat response with respect to the plutonium distribution inside the waste can. The sensitivity of the scanner is 200 mg of Pu per can at 2 sigma level and 20% accuracy for a total scan time of 2000 sec. The assay results of typical waste cans and comparison of a few of these with chemical assay results are presented. This non-destructive method is fast, simple and has satisfactory accuracy. (author)

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

The Mayak Worker Dosimetry System (MWDS 2013): soluble plutonium retention in the lungs of an occupationally exposed USTUR case

International Nuclear Information System (INIS)

Tolmachev, S. Y.; Avtandilashvili, M.; Martinez, F.; Thomas, E. M.; Miller, F. L.; Nielsen, C. E.; Puncher, M.; Morgan, W. F.; Birchall, A.

2017-01-01

For the first time, plutonium retention in human upper airways was investigated based on the dosimetric structure of the human respiratory tract proposed by the International Commission on Radiological Protection (ICRP). This paper describes analytical work methodology, case selection criteria, and summarizes findings on soluble (ICRP 68 Type M material) plutonium distribution in the lungs of a former nuclear worker occupationally exposed to plutonium nitrate [ 239 Pu(NO 3 ) 4 ]. Thirty-eight years post-intake, plutonium was found to be uniformly distributed between bronchial (BB), bronchiolar (bb) and alveolar-interstitial (AI) dosimetric compartments as well as between the left and right lungs. 239+240 Pu and 238 Pu total body activity was estimated to be 2333 ± 23 and 42.1 ± 0.7 Bq, respectively. The results of this work provide key information on the extent of plutonium binding in the upper airways of the human respiratory tract. (authors)

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. �

Calculation of Doses Due to Accidentally Released Plutonium From An LMFBR

Energy Technology Data Exchange (ETDEWEB)

Fish, B.R.

2001-08-07

Experimental data and analytical models that should be considered in assessing the transport properties of plutonium aerosols following a hypothetical reactor accident have been examined. Behaviors of released airborne materials within the reactor containment systems, as well as in the atmosphere near the reactor site boundaries, have been semiquantitatively predicted from experimental data and analytical models. The fundamental chemistry of plutonium as it may be applied in biological systems has been used to prepare models related to the intake and metabolism of plutonium dioxide, the fuel material of interest. Attempts have been made to calculate the possible doses from plutonium aerosols for a typical analyzed release in order to evaluate the magnitude of the internal exposure hazards that might exist in the vicinity of the reactor after a hypothetical LMFBR (Liquid-Metal Fast Breeder Reactor) accident. Intake of plutonium (using data for {sup 239}Pu as an example) and its distribution in the body were treated parametrically without regard to the details of transport pathways in the environment. To the extent possible, dose-response data and models have been reviewed, and an assessment of their adequacy has been made so that recommended or preferred practices could be developed.

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 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

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

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

Plutonium chemistry: a synthesis of experimental data and a quantitative model for plutonium oxide solubility

International Nuclear Information System (INIS)

Haschke, J.M.; Oversby, V.M.

2002-01-01

The chemistry of plutonium is important for assessing potential behavior of radioactive waste under conditions of geologic disposal. This paper reviews experimental data on dissolution of plutonium oxide solids, describes a hybrid kinetic-equilibrium model for predicting steady-state Pu concentrations, and compares laboratory results with predicted Pu concentrations and oxidation-state distributions. The model is based on oxidation of PuO 2 by water to produce PuO 2+x , an oxide that can release Pu(V) to solution. Kinetic relationships between formation of PuO 2+x , dissolution of Pu(V), disproportionation of Pu(V) to Pu(IV) and Pu(VI), and reduction of Pu(VI) are given and used in model calculations. Data from tests of pyrochemical salt wastes in brines are discussed and interpreted using the conceptual model. Essential data for quantitative modeling at conditions relevant to nuclear waste repositories are identified and laboratory experiments to determine rate constants for use in the model are discussed

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

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 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

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

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.)

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)

Recovery of plutonium by pyroredox processing

International Nuclear Information System (INIS)

McNeese, J.A.; Bowersox, D.F.; Christensen, D.C.

1985-09-01

Using pyrochemical oxidation and reduction, we have developed a process to recover the plutonium in impure scrap with less than 95% plutonium. This plutonium metal was further purified by pyrochemical electrorefining. During development of the procedures, depleted electrorefining anodes were processed, and over 80% of the plutonium was recovered as high-purity metal in one electrorefining cycle. Over 40 kg of plutonium has been recovered from 55 kg of impure anodes with our procedures. 6 refs., 7 figs., 4 tabs

Recovery of plutonium by pyroredox processing

International Nuclear Information System (INIS)

McNeese, J.A.; Bowersox, D.F.; Christensen, D.C.

1985-01-01

Using pyrochemical oxidation and reduction, we have developed a process to recover the plutonium in impure scrap with less than 95% plutonium. This plutonium metal was further purified by pyrochemical electrorefining. During development of the procedures, depleted electrorefining anodes were processed, and over 80% of the plutonium was recovered as high-purity metal in one electrorefining cycle. Over 40 kg of plutonium has been recovered from 55 kg of impure anodes with our procedures. 6 refs., 2 figs., 5 tabs

The use of calorimetry for plutonium assay

International Nuclear Information System (INIS)

Mason, J.A.

1982-12-01

Calorimetry is a technique for measuring the thermal power of heat-producing substances. The technique may be applied to the measurement of plutonium-bearing materials which evolve heat as a result of alpha and beta decay. A calorimetric measurement of the thermal power of a plutonium sample, combined with a knowledge or measurement of the plutonium isotopic mass ratios of the sample provides a convenient and accurate, non-destructive measure of the total plutonium mass of the sample. The present report provides a description, and an assessment of the calorimetry technique applied to the assay of plutonium-bearing materials. Types and characteristics of plutonium calorimeters are considered, as well as calibration and operating procedures. The instrumentation used with plutonium calorimeters is described and the use of computer control for calorimeter automation is discussed. A critical review and assessment of plutonium calorimetry literature since 1970 is presented. Both fuel element and plutonium-bearing material calorimeters are considered. The different types of plutonium calorimeters are evaluated and their relative merits are discussed. A combined calorimeter and gamma-ray measurement assay system is considered. The design principles of plutonium assay calorimeters are considered. An automatic, computer-based calorimeter control system is proposed in conjunction with a general plutonium assay calorimeter design. (author)

Analytic determination of plutonium in the environment; Determination analytique du plutonium dans l'environnement

Energy Technology Data Exchange (ETDEWEB)

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

1967-07-01

The work described in this report was undertaken with a view to determining the plutonium content in the fall-out from nuclear explosions. In the first part are described in turn the importance of the problems due to the plutonium, the physico-chemical properties of the radioelement and the biological dangers which it presents. A detailed and critical analysis is made of the radio-toxicological determination of the plutonium as reported in the literature prior to this report. The second part consists in the presentation of a judicious choice of techniques making it possible to determine plutonium in air, rain-water, soils and ash. After a detailed description of the measurement equipment and the operational techniques which have been developed, a justification of these techniques is given with particular reference to their sensitivity and specificity. After a brief conclusion concerning the preceding chapters, the results are presented. These are then discussed in the ease of each element in which the plutonium has been determined. This discussion is concluded by a consideration of the importance of the occurrence of fall-out plutonium on problems relating to public health. From a consideration of 200 analyses carried out, it is concluded that the contribution of plutonium to the exposure of populations is still very small compared to that of natural radiation and that due to such fission products as strontium 90. The report includes 63 literature references, 26 figures and 11 tables. (author) [French] Les travaux decrits dans ce memoire ont ete entrepris et eflectues dans le but de mettre en evidence le plutonium des retombees radioactives consecutives aux explosions nucleaires. Dans la premiere partie nous etudions successivement l'importance des problemes poses par le plutonium puis les proprietes physicochimiques du radioelement et les dangers qu'il presente du point de vue biologique. Nous effectuons une analyse detaillee et critique des techniques

Experimental study of the higher isotopes of plutonium in the coupled fast-thermal assembly Ermine

International Nuclear Information System (INIS)

Bioux, Philippe.

1973-01-01

The most important results so far of the plutonium isotopes programme carried out in Ermine are reviewed. The results were obtained on four networks: one with uranium fuel and three with plutonium. The choice of these four networks was essentially based on the energy range of their nuclear reactions, wide enough to include the large reactor energy range, and yet realistic, with a neutron energy distribution in the 4 networks which is never very far from that encountered in a power reactor. The information relative to the high isotopes of plutonium which were obtained in these networks mostly came from: the fission indices measured in the 4 networks, the study of the balance in the two media at k(infinite)=1, reactivity measurements on cell replacements and on various plutonium samples, carried out on the three plutonium fuel networks [fr

Considerations in the assessment of plutonium deposition in man

International Nuclear Information System (INIS)

Voelz, G.; Umbarger, J.; McInroy, J.; Healy, J.

1975-01-01

Data from human cases of plutonium inhalation are used to illustrate several important problems in the current methods of estimating plutonium body burdens. Individuals exposed to 238 PuO 2 particles in a highly insoluble matrix showed an unusually slow rising urinary excretion curve over 300 to 400 days. In vivo chest counts during the first 6 months estimated lung burdens to be 10 to 30 nCi, but urinary excretion methods calculate residual systematic body burdens of 50 to 100 nCi at 1200 days after exposure. Current assumptions used in the in vivo calibration do not consider possible lung distribution of particulates soon after exposure that could alter the interpretation significantly. Tissue analysis of a lung from another case after recent inhalation exposure shows a significantly lesser concentration of plutonium in the subpleural region--the principal region of plutonium measurement by in vivo chest counting--as compared to distributions found years after exposure. Tissue analyses indicate that urinary excretion estimates of body burden over the long term tend to err on the high side up to a factor of 5 or more. This procedure serves well for the purpose of protection of workers, but high estimates can lead to unnecessary job reassignments for the individual worker and can cause misleading conclusions when such data is used uncritically for reference in health effects studies. Additional research is needed to improve urinary excretion data analysis to reflect newer information derived from tissue data and to seek further understanding of the sources of variation in in vivo counting technology so it can be used with greater confidence

Partitioning of plutonium and uranium in aqueous medium using hydroxyurea as reducing agent

International Nuclear Information System (INIS)

Sivakumar, P.; Subba Rao, R.V.; Meenakshi, S.

2012-01-01

A new process for the partitioning of plutonium and uranium during the reprocessing of spent fuel discharged from fast reactor was optimised using hydroxyurea (HU) as a reductant. Stoichiometric ratio of HU required for the reduction of Pu(IV) was studied. The effect of concentration of uranium, plutonium and acidity on the distribution ratio (Kd) of Pu in the presence of HU was studied. The effect of HU in further purification of Pu such as solvent extraction and precipitation of plutonium as oxalate was also studied. The results of the study indicate that Pu and U can be separated from each other using HU as reductant. (author)

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

Uncertainties on lung doses from inhaled plutonium.

Science.gov (United States)

Puncher, Matthew; Birchall, Alan; Bull, Richard K

2011-10-01

In a recent epidemiological study, Bayesian uncertainties on lung doses have been calculated to determine lung cancer risk from occupational exposures to plutonium. These calculations used a revised version of the Human Respiratory Tract Model (HRTM) published by the ICRP. In addition to the Bayesian analyses, which give probability distributions of doses, point estimates of doses (single estimates without uncertainty) were also provided for that study using the existing HRTM as it is described in ICRP Publication 66; these are to be used in a preliminary analysis of risk. To infer the differences between the point estimates and Bayesian uncertainty analyses, this paper applies the methodology to former workers of the United Kingdom Atomic Energy Authority (UKAEA), who constituted a subset of the study cohort. The resulting probability distributions of lung doses are compared with the point estimates obtained for each worker. It is shown that mean posterior lung doses are around two- to fourfold higher than point estimates and that uncertainties on doses vary over a wide range, greater than two orders of magnitude for some lung tissues. In addition, we demonstrate that uncertainties on the parameter values, rather than the model structure, are largely responsible for these effects. Of these it appears to be the parameters describing absorption from the lungs to blood that have the greatest impact on estimates of lung doses from urine bioassay. Therefore, accurate determination of the chemical form of inhaled plutonium and the absorption parameter values for these materials is important for obtaining reliable estimates of lung doses and hence risk from occupational exposures to plutonium.

Plutonium in a grassland ecosystem. [Rocky Flats Plant

Energy Technology Data Exchange (ETDEWEB)

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, /sup 238/Pu and /sup 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.

Plutonium contamination in soils in open space and residential areas near Rocky Flats, Colorado

International Nuclear Information System (INIS)

Litaor, M.I.

1999-01-01

Spatial analysis of the 240 Pu: 239 Pu isotopic ratio of 42 soil samples collected around Rocky Flats Plant near Golden, Colorado, was conducted to assess the effect of Rocky Flats Plant activity on the soil environment. Two probability maps that quantified the uncertainty of the spatial distribution of plutonium isotopic ratios were constructed using the sequential Gaussian simulation technique (sGs). Assuming a plutonium isotopic ratio range of 0.152 ± 0.003 to 0.169 ± 0.009 is characteristic to global fallout in Colorado, and a mean value of 0.155 is representative for the Rocky Flats Plant area, the main findings of the current work were (1) the areas northwest and southwest of Rocky Flats Plant exhibited a plutonium ratio ≥0.155, this were minimally impacted by the plant activity; (2) he study area east of Rocky Flats Plant exhibited a plutonium isotopic ratio ≤0.155, which is a definitive indicator of Rocky Flats Plant-derived plutonium; and (3) inventory calculations across the study area exhibited large standard error of estimates. These errors were originated from the high variability in plutonium activity over a small sampling scale and the uncertainty in the global fallout isotopic ratio. Using the mean simulated estimates of plutonium isotopic ratio, coupled with plutonium activity measured at 11 soil pits and additional plutonium information published elsewhere, the plutonium loading on the open space and residential areas amounted to 111.2 GBq, with a standard error of estimate of 50.8 GBq

Recovery studies for plutonium machining oil coolant

International Nuclear Information System (INIS)

Navratil, J.D.; Baldwin, C.E.

1977-01-01

Lathe coolant oil, contaminated with plutonium and having a carbon tetrachloride diluent, is generated in plutonium machining areas at Rocky Flats. A research program was initiated to determine the nature of plutonium in this mixture of oil and carbon tetrachloride. Appropriate methods then could be developed to remove the plutonium and to recycle the oil and carbon tetrachloride. Studies showed that the mixtures of spent oil and carbon tetrachloride contained particulate plutonium and plutonium species that are soluble in water or in oil and carbon tetrachloride. The particulate plutonium was removed by filtration; the nonfilterable plutonium was removed by adsorption on various materials. Laboratory-scale tests indicated the lathe-coolant oil mixture could be separated by distilling the carbon tetrachloride to yield recyclable products

Los Alamos Plutonium Facility Waste Management System

International Nuclear Information System (INIS)

Smith, K.; Montoya, A.; Wieneke, R.; Wulff, D.; Smith, C.; Gruetzmacher, K.

1997-01-01

This paper describes the new computer-based transuranic (TRU) Waste Management System (WMS) being implemented at the Plutonium Facility at Los Alamos National Laboratory (LANL). The Waste Management System is a distributed computer processing system stored in a Sybase database and accessed by a graphical user interface (GUI) written in Omnis7. It resides on the local area network at the Plutonium Facility and is accessible by authorized TRU waste originators, count room personnel, radiation protection technicians (RPTs), quality assurance personnel, and waste management personnel for data input and verification. Future goals include bringing outside groups like the LANL Waste Management Facility on-line to participate in this streamlined system. The WMS is changing the TRU paper trail into a computer trail, saving time and eliminating errors and inconsistencies in the process

The Amarillo National Resource Center for Plutonium. Quarterly progress detailed report, 1 November 1996--31 January 1997

Energy Technology Data Exchange (ETDEWEB)

NONE

1997-03-01

Progress for this quarter is given for each of the following Center programs: (1) plutonium information resource; (2) advisory function (DOE and state support); (3) environmental, public health and safety; (3) communication, education, and training; and (4) nuclear and other material studies. Both summaries of the activities and detailed reports are included.

Plutonium use in foreign countries (01)

International Nuclear Information System (INIS)

Otagaki, Takao

2002-03-01

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 experience of plutonium recycling have been accumulated until now. Thus, the status of plutonium recycling up to the end of 2001 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 recently appears the move of recycling 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 on plutonium inventories of foreign countries were collected. (author)

Plutonium use in foreign countries (99)

International Nuclear Information System (INIS)

Otagaki, Takao

2000-03-01

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 experience of plutonium recycling have been accumulated until now. Thus, the status of plutonium recycling up to the end of 1999 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 recently appears the move to recycling 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 on plutonium inventories of foreign counties were collected. (author)

Plutonium use in foreign countries (02)

International Nuclear Information System (INIS)

Otagaki, Takao

2003-02-01

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 experience of plutonium recycling have been accumulated until now. Thus, the status of plutonium recycling up to the end of 2002 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 recently appears the move of recycling 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 Oside (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 on plutonium inventories of foreign countries were collected. (author)

Plutonium use in foreign countries. (04)

International Nuclear Information System (INIS)

Otagaki, Takao

2005-03-01

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 experience of plutonium recycling have been accumulated until now. Thus, the status of plutonium recycling up to the end of 2004 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 limited amount 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 on plutonium inventories of foreign countries were collected. (author)

Laboratory-scale evaluations of alternative plutonium precipitation methods

International Nuclear Information System (INIS)

Martella, L.L.; Saba, M.T.; Campbell, G.K.

1984-01-01

Plutonium(III), (IV), and (VI) carbonate; plutonium(III) fluoride; plutonium(III) and (IV) oxalate; and plutonium(IV) and (VI) hydroxide precipitation methods were evaluated for conversion of plutonium nitrate anion-exchange eluate to a solid, and compared with the current plutonium peroxide precipitation method used at Rocky Flats. Plutonium(III) and (IV) oxalate, plutonium(III) fluoride, and plutonium(IV) hydroxide precipitations were the most effective of the alternative conversion methods tested because of the larger particle-size formation, faster filtration rates, and the low plutonium loss to the filtrate. These were found to be as efficient as, and in some cases more efficient than, the peroxide method. 18 references, 14 figures, 3 tables

The plutonium danger

International Nuclear Information System (INIS)

Ruiter, W. de

1983-01-01

Nobody can ignore the fact that plutonium is potentially very dangerous and the greatest danger concerning it lies in the spreading of nuclear weapons via nuclear energy programmes. The following seven different attitudes towards this problem are presented and discussed: 1) There is no connection between peaceful and military applications; 2) The problem cannot be prevented; 3) A technical solution must be found; 4) plutonium must be totally inaccessible to countries involved in acquiring nuclear weapons; 5) The use of plutonium for energy production should only occur in one multinational centre; 6) Dogmas in the nuclear industry must be enfeebled; 7) All developments in this area should stop. (C.F.)

Plutonium in Southern Hemisphere ocean Waters

DEFF Research Database (Denmark)

Hirose, K.; Aoyama, M.; Gastaud, J.

2013-01-01

Plutonium in seawater collected by the BEAGLE2003 cruise was determined using ICP- SF-MS and alpha spectrometry after Fe co-precipitation and radiochemical purification. Levels and distributions of dissolved plutonium activity concentrations in Southern Hemisphere ocean waters are summarized here......, including historical data. Pu-239 concentrations in surface water----of the central South Pacific (32.5 °S) in 2003 were around 1 mBq/m3. The 239Pu concentrations in the Indian Ocean surface waters (20°S) were similar to that in the South Pacific, whereas the 239Pu concentrations in the South Atlantic...... surface waters (30°S) were markedly lower than those in the South Pacific and Indian Oceans. The 239Pu vertical profile pattern was similar to that in the North Pacific subtropical gyre, although 239Pu concentrations in the deep South Pacific were significantly lower than those in the North Pacific. One...

Some investigations into the behaviour of plutonium in the marine environment

International Nuclear Information System (INIS)

Hetherington, J.A.; Jefferies, D.F.; Lovett, M.B.

1975-01-01

Plutonium and other transuranic elements are produced during the operation of magnox reactors, although they do not usually present any problems of waste management until the fuel reaches the reprocessing stage. At this stage one of the chief aims is to separate and recover the plutonium from the depleted uranium and the fission products, the incentive being the value of plutonium itself as a nuclear fuel particularly for the fast breeder reactors. For this reason the amounts of plutonium appearing in the low activity waste streams for discharge to the environment are usually small, and their radiological impact insignificant compared with that of the more abundant fission products. However, with the prospect of use of large quantities of plutonium in the fast reactors, considerable interest surrounds all aspects of the properties of plutonium, and in an attempt to give a fuller understanding of the behaviour of plutonium in the marine environment use has been made of the small amounts which have been discharged in recent years to the north-east Irish Sea from the fuel reprocessing plant at Windscale in Cumbria. Details of the amounts of 239 Pu and 240 Pu discharged to sea are given and the resultant measured concentrations of the isotopes in the water throughout the Irish Sea are shown. The distribution of plutonium in sea water is shown to follow the same basic pattern as the fission products, details of which have been reported previously. By comparing the concentration gradients with distance from the point of discharge for plutonium and caesium, a value for the rate of loss of plutonium from the water to the other important compartment, namely the sediment, has been deduced. Measurements have been made of 239 Pu and 240 Pu in seabed and estuarine sediments and by combining these with the water data values of the concentration factor for the nuclide in sediment have been calculated. The results of a number of core samples have been used to calculate an

Frequency distribution, isotopic composition and physical characterization of plutonium-bearing particles from the Fig-Quince zone on Runit Island, Enewetak Atoll

International Nuclear Information System (INIS)

Hamilton, T.F.; Martinelli, R.E.; Kehl, S.R.; Rivers, A.N.; Brown, T.A.; Tumey, S.J.; Jernstroeem, J.; Williams, R.W.

2009-01-01

Runit Island on Enewetak Atoll was very heavily impacted by the U.S. nuclear testing campaign in the northern Marshall Islands (1946-58). The primary source of contamination on Runit Island was the 1958 Quince safety test where a large quantity of device plutonium (Pu) was scattered over the area near the GZ. A second low-yield device was detonated on the same site 10 days later, further disturbing the soil and leaving behind a very heterogeneous pattern of contamination including milligram-size particles of plutonium. A limited cleanup of the Fig-Quince zone was carried out in 1979. During this period, the effectiveness of the cleanup operations was primarily evaluated on the basis of bulk soil concentration data with little consideration given to the heterogeneity and long-term material-, biological-, and environmental-specific impacts of residual high activity (hot) particle contamination. The aim of the present study was twofold; (i) to characterize the levels and distribution of residual contamination in the Fig-Quince zone, and (ii) to develop pertinent data on the frequency distribution, elemental and isotopic composition, and physico-chemical properties of hot particles isolated from surface soils from Fig-Quince with a view towards providing recommendations on the future management and possible cleanup of the site. Today, Runit Island remains under an administrative quarantine. (author)

Studies on O/M ratio determination in uranium oxide, plutonium oxide and uranium-plutonium mixed oxide

International Nuclear Information System (INIS)

Sampath, S.; Chawla, K.L.

1975-01-01

Thermogravimetric studies were carried out in unsintered and sintered samples of uranium oxide, plutonium oxide and uranium-plutonium mixed oxide under different atmospheric conditions (air, argon and moist argon/hydrogen). Moisture loss was found to occur below 200 0 C for uranium dioxide samples, upto 700 0 C for sintered plutonium dioxide and negligible for sintered samples. The O/M ratios for non-stoichiometric uranium dioxide (sintered and unsintered), plutonium dioxide and mixed uranium and plutonium oxides (sintered) could be obtained with a precision of +- 0.002. Two reference states UOsub(2.000) and UOsub(2.656) were obtained for uranium dioxide and the reference state MOsub(2.000) was used for other cases. For unsintered plutonium dioxide samples, accurate O/M ratios could not be obtained of overlap of moisture loss with oxygen loss/gain. (author)

The plutonium challenge for the future

International Nuclear Information System (INIS)

Gray, L.W.

2000-01-01

In this paper author deal with the weapons-usable plutonium and with the possibilities of their managing. Russia has not disclosed the amount of plutonium produced, but various estimates indicate that the production was about 130 tonnes. Production has been curtailed in Russia; three dual-purpose reactors still produce weapons-grade plutonium - two at Tomsk-7 (renamed Seversk) and one at Krasnoyarsk-26 (renamed Zheleznogorsk Mining and Chemical Combine). In a 1994 United States-Russian agreement that has yet to enter into force, Russia agreed to close the remaining operating reactors by the year 2000. Treaties between the United States and Russia have already cut the number of nuclear warheads from more than 10,000 to about 6,000 under START 1, which has been ratified, and to about 3,500 under START 2, which still awaits approval. If Russia and the United States conclude START 3, that number could drop to between 2,000 and 2,500. On September 2, 1998, the Presidents of the United States and Russia signed the 'Joint statement of principles for Management and Disposition of Plutonium, Designated as No Longer Required for Defense Purposes.' In this joint statement the Presidents affirm the intention of each country to remove by stages approximately 50 metric tons of plutonium and to convert the nuclear weapons programs, and to convert this material so that it can never be used in nuclear weapons. These 100 tonne of plutonium must be managed in proper way such that it becomes neither a proliferation for an environmental risk. The United States has proposed that it manage it's 50 tonnes by a dual approach-once through MOX burning of a portion of the plutonium and immobilization in a ceramic matrix followed by en- casement in high level waste glass. Russia has proposed that it manage its full 50 tonnes by burning in a reactor. The MOX program in the United States would bum the cleaner plutonium metal and residues. Weapons components would be converted to plutonium oxide

Geochemical association of plutonium in marine sediments from Palomares (Spain)

International Nuclear Information System (INIS)

Anton, M.P.; Gasco, C.; Sanchez-Cabeza, J.A.; Pujol, L.

1994-01-01

The geochemical association of plutonium in sediments from the marine ecosystem of Palomares has been studied. A sequential leaching technique using selective extractants has been employed to determine the percentages of Pu in the following forms: (a) readily available, (b) exchangeable and adsorbed to specific sites, (c) associated with organic matter, (d) sesquioxides, (e) residual. Plutonium was found to be associated mainly with phases (c), (d) and (e), and therefore, appears to be relatively immobile and not readily available to bottom feeding biota. The effect of different source terms on Pu distribution is also discussed. (orig.)

Selective leaching studies of deep-sea sediments loaded with americium, neptunium and plutonium

International Nuclear Information System (INIS)

Cole, T.G.; Higgo, J.J.W.; Cronan, D.S.; Rees, L.V.C.

1984-07-01

A series of selective leaching experiments were undertaken to investigate the solid phase speciation and distribution of americium, neptunium and plutonium which had been experimentally loaded onto different marine sediment types. The chemical leaches employed showed rather poor selectivity but certain trends were evident. Adsorption was not by ion exchange. Americium showed a preferential affinity for carbonate and plutonium for organic matter. Neptunium appeared to have no preferential affinities. Americium was sorbed by acetic acid residues (CaCO 3 removed) and by unleached carbonate-rich sediments with equal efficiency. This indicates that it is able to diversify its solid phase affinity/distribution depending upon which solid phases are available. (author)

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

Monitoring the risks of plutonium

International Nuclear Information System (INIS)

Holliday, B.

1978-01-01

The difficulties in monitoring the environment in work areas where plutonium is handled are identified and both continuous and personal air sampling techniques considered. Methods of estimating the amounts of plutonium retained in the body are: (1) Direct external counting over the chest of the 'soft' low energy X-rays and gamma rays emitted by the plutonium deposited in the lungs. (2) Measuring plutonium excreted in urine. (3) Analysing faeces soon after a suspected contamination. Limitation of these techniques are discussed and it is shown that estimating the amount of plutonium in the body, or a specific organ, is extremely difficult, both because of the lack of sensitivity of the measuring techniques (especially chest scanning) and because of the problems in interpreting data, stemming from a lack of knowledge of crucial characteristics of the inhaled plutonium (such as particle size and solubility). Nevertheless it is felt that the judicious integration of all the options creates a level of certainty that no individual technique can possibly inspire. (U.K.)

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

Low-Level Plutonium Bioassay Measurements at the Lawrence Livermore National Laboratory

Energy Technology Data Exchange (ETDEWEB)

Hamilton, T; Brown, T; Hickman, D; Marchetti, A; Williams, R; Kehl, S

2007-06-18

Plutonium-239 ({sup 239}Pu) and plutonium-240 ({sup 240}Pu) are important alpha emitting radionuclides contained in radioactive debris from nuclear weapons testing. {sup 239}Pu and {sup 240}Pu are long-lived radionuclides with half-lives of 24,400 years and 6580 years, respectively. Concerns over human exposure to plutonium stem from knowledge about the persistence of plutonium isotopes in the environment and the high relative effectiveness of alpha-radiation to cause potential harm to cells once incorporated into the human body. In vitro bioassay tests have been developed to assess uptakes of plutonium based on measured urinary excretion patterns and modeled metabolic behaviors of the absorbed radionuclides. Systemic plutonium absorbed by the deep lung or from the gastrointestinal tract after ingestion is either excreted or distributed to other organs, primarily to the liver and skeleton, where it is retained for biological half-times of around 20 and 50 years, respectively. Dose assessment and atoll rehabilitation programs in the Marshall Islands have historically given special consideration to residual concentrations of plutonium in the environment even though the predicted dose from inhalation and/or ingestion of plutonium accounts for less than 5% of the annual effective dose from exposure to fallout contamination. Scientists from the Lawrence Livermore National Laboratory (LLNL) have developed a state-of-the-art bioassay test to assess urinary excretion rates of plutonium from Marshallese populations. This new heavy-isotope measurement system is based on Accelerator Mass Spectrometry (AMS). The AMS system at LLNL far exceeds the standard measurement requirements established under the latest United States Department of Energy (DOE) regulation, 10CFR 835, for occupational monitoring of plutonium, and offers several advantages over classical as well as competing new technologies for low-level detection and measurement of plutonium isotopes. The United States

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.

Plutonium use - Present status and prospects

International Nuclear Information System (INIS)

Dievoet, J. van; Fossoul, E.; Jonckheere, E.; Bemden, E. van den

1977-01-01

The use of plutonium in thermal and fast reactors is a demonstrated, if not proven, technology. Moreover, plutonium is being produced in increasing quantities. Evaluation of this production on a world scale shows that it would be theoretically possible to construct numerous breeders and thus to make the best use of plutonium, while considerably reducing uranium consumption. This source of plutonium is nevertheless dependent on the reprocessing of irradiated fuel. Long delays in installing and adequate world reprocessing capacity are weakening the prospects for introducing breeders. Furthermore, the critical situation regarding reprocessing may delay the development of complementary reprocessing methods for fuels with a high plutonium content and high burnup. The recycling of plutonium is now a well-known technique and any objections to it hardly bear analysis. Utilization of plutonium offers an appreciable saving in terms of uranium and separative work units; and it can also be shown that immediate reprocessing of the recycling fuel is not essential for the economics of the concept. Temporary storage of recycled fuel is a particularly safe form of concentrating plutonium, namely in irradiated plutonium-bearing fuel assemblies. Finally, recycling offers such flexibility that it represents no obstacle to fuel management at power plants with light-water reactors. These strategic considerations imply that the technology of using plutonium for fabricating thermal or fast reactor fuels is both technically reliable and economically viable. The methods used in industrial facilities are fully reassuring in this respect. Although various unsolved problems exist, none seems likely to impede current developments, while the industrial experience gained has enabled the economics and reliability of the methods to be improved appreciably. Apart from the techno-economic aspects, the plutonium industry must face extremely important problems in connection with the safety of personnel

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

Solubility of plutonium from rumen contents of cattle grazing on plutonium-contaminated desert vegetation in in vitro bovine gastrointestinal fluids

International Nuclear Information System (INIS)

Barth, J.

1975-01-01

Rumen contents of cattle grazing on plutonium-contaminated desert vegetation at the Nevada Test Site were incubated in simulated bovine gastrointestinal fluids to study the alimentary solubility of plutonium. Trials were run during November 1973, and during February, May, July and August 1974. During the May and July trials, a large increase in plutonium solubility accompanied by a marked reduction in plutonium concentration of the rumen contents was observed concurrently with a reduction in intake of Eurotia lanata and an increase in the intake of Oryzopsis hymenoides or Sitanion jubatum. However, during the November, February, and August trials, comparatively high concentration of plutonium, but low plutonium solubility, was associated with high levels of Eurotia lanata in the rumen contents. Plutonium-238 was generally more soluble than plutonium-239 in these fluids. Ratios of the percentage of soluble plutonium-238 to the percentage of soluble plutonium-239 varied fro []1:1 to 18:1 on a radioactivity basis. (auth)

Plutonium metal burning facility

International Nuclear Information System (INIS)

Hausburg, D.E.; Leebl, R.G.

1977-01-01

A glove-box facility was designed to convert plutonium skull metal or unburned oxide to an oxide acceptable for plutonium recovery and purification. A discussion of the operation, safety aspects, and electrical schematics are included

Analytic determination of plutonium in the environment; Determination analytique du plutonium dans l'environnement

Energy Technology Data Exchange (ETDEWEB)

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

1967-07-01

The work described in this report was undertaken with a view to determining the plutonium content in the fall-out from nuclear explosions. In the first part are described in turn the importance of the problems due to the plutonium, the physico-chemical properties of the radioelement and the biological dangers which it presents. A detailed and critical analysis is made of the radio-toxicological determination of the plutonium as reported in the literature prior to this report. The second part consists in the presentation of a judicious choice of techniques making it possible to determine plutonium in air, rain-water, soils and ash. After a detailed description of the measurement equipment and the operational techniques which have been developed, a justification of these techniques is given with particular reference to their sensitivity and specificity. After a brief conclusion concerning the preceding chapters, the results are presented. These are then discussed in the ease of each element in which the plutonium has been determined. This discussion is concluded by a consideration of the importance of the occurrence of fall-out plutonium on problems relating to public health. From a consideration of 200 analyses carried out, it is concluded that the contribution of plutonium to the exposure of populations is still very small compared to that of natural radiation and that due to such fission products as strontium 90. The report includes 63 literature references, 26 figures and 11 tables. (author) [French] Les travaux decrits dans ce memoire ont ete entrepris et eflectues dans le but de mettre en evidence le plutonium des retombees radioactives consecutives aux explosions nucleaires. Dans la premiere partie nous etudions successivement l'importance des problemes poses par le plutonium puis les proprietes physicochimiques du radioelement et les dangers qu'il presente du point de vue biologique. Nous effectuons une analyse detaillee et critique des techniques

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

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

Plutonium isotopic measurements by gamma-ray spectroscopy

International Nuclear Information System (INIS)

Haas, F.X.; Lemming, J.F.

1976-01-01

A nondestructive technique is described for calculating plutonium-238, plutonium-240, plutonium-241 and americium-241 relative to plutonium-239 from measured peak areas in the high resolution gamma-ray spectra of solid plutonium samples. Gamma-ray attenuation effects were minimized by selecting sets of neighboring peaks in the spectrum whose components are due to the different isotopes. Since the detector efficiencies are approximately the same for adjacent peaks, the accuracy of the isotopic ratios is dependent on the half-lives, branching intensities, and measured peak areas. The data presented describe the results obtained by analyzing gamma-ray spectra in the energy region from 120 to 700 keV. Most of the data analyzed were obtained from plutonium material containing 6 percent plutonium-240. Sample weights varied from 0.25 g to approximately 1.2 kg. The methods were also applied to plutonium samples containing up to 23 percent plutonium-240 with weights of 0.25 to 200 g. Results obtained by gamma-ray spectroscopy are compared to chemical analyses of aliquots taken from the bulk samples

Independent verification of plutonium decontamination on Johnston Atoll (1992--1996)

International Nuclear Information System (INIS)

Wilson-Nichols, M.J.; Wilson, J.E.; McDowell-Boyer, L.M.; Davidson, J.R.; Egidi, P.V.; Coleman, R.L.

1998-05-01

The Field Command, Defense Special Weapons Agency (FCDSWA) (formerly FCDNA) contracted Oak Ridge National Laboratory (ORNL) Environmental Technology Section (ETS) to conduct an independent verification (IV) of the Johnston Atoll (JA) Plutonium Decontamination Project by an interagency agreement with the US Department of Energy in 1992. The main island is contaminated with the transuranic elements plutonium and americium, and soil decontamination activities have been ongoing since 1984. FCDSWA has selected a remedy that employs a system of sorting contaminated particles from the coral/soil matrix, allowing uncontaminated soil to be reused. The objective of IV is to evaluate the effectiveness of remedial action. The IV contractor's task is to determine whether the remedial action contractor has effectively reduced contamination to levels within established criteria and whether the supporting documentation describing the remedial action is adequate. ORNL conducted four interrelated tasks from 1992 through 1996 to accomplish the IV mission. This document is a compilation and summary of those activities, in addition to a comprehensive review of the history of the project

PROJECT EXPERIENCE REPORT DEMOLITION OF HANFORDS 233-S PLUTONIUM CONCENTRATION FACILITY

International Nuclear Information System (INIS)

BERLIN, G.T.; ORGILL, T.K.

2004-01-01

This report provides a summary of the preparation, operations, innovative work practices, and lessons learned associated with demolition of the 2334 Plutonium Concentration Facility. This project represented the first open-air demolition of a highly-contaminated plutonium facility at the Hanford Site. This project may also represent the first plutonium facility in the US. Department of Energy (DOE) complex to have been demolished without first decontaminating surfaces to near ''free release'' standards. Demolition of plutonium contaminated structures, if not properly managed, can subject cleanup personnel and the environment to significant risk. However, with proper sequencing and innovative use of commercially available equipment, materials, and services, this project demonstrated that a plutonium processing facility can be demolished while avoiding the need to perform extensive decontamination or to construct large enclosures. This project utilized an excavator with concrete shears, diamond circular saws, water misting and fogging equipment, commercially available fixatives and dust suppressants, conventional mobile crane and rigging services, and near real-time modeling of meteorological and radiological conditions. Following a significant amount of preparation, actual demolition of the 233-S Facility began in October 2003 and was completed in late April 2004. The knowledge and experience gained on this project are important to the Hanford Site as additional plutonium processing facilities are scheduled for demolition in the near future. Other sites throughout the DOE Complex may also be faced with similar challenges. Numerous innovations and effective work practices were implemented on this project. Accordingly, a series of ''Lessons Learned and Innovative Practices Fact Sheets'' were developed and are included as an appendix to this report. This collection of fact sheets is not intended to capture every innovative work practice and lesson learned, but rather

PROJECT EXPERIENCE REPORT DEMOLITION OF HANFORDS 233-S PLUTONIUM CONCENTRATION FACILITY

International Nuclear Information System (INIS)

BERLIN, G.T.

2004-01-01

This report provides a summary of the preparation, operations, innovative work practices, and lessons learned associated with demolition of the 2334 Plutonium Concentration Facility. This project represented the first open-air demolition of a highly-contaminated plutonium facility at the Hanford Site. This project may also represent the first plutonium facility in the US. Department of Energy (DOE) complex to have been demolished without first decontaminating surfaces to near ''free release'' standards. Demolition of plutonium contaminated structures, if not properly managed, can subject cleanup personnel and the environment to significant risk. However, with proper sequencing and innovative use of commercially available equipment, materials, and services, this project demonstrated that a plutonium processing facility can be demolished while avoiding the need to perform extensive decontamination or to construct large enclosures. This project utilized an excavator with concrete shears, diamond circular saws, water misting and fogging equipment, commercially available fixatives and dust suppressants, conventional mobile crane and rigging services, and near real-time modeling of meteorological and radiological conditions. Following a significant amount of preparation, actual demolition of the 2333 Facility began in October 2003 and was completed in late April 2004. The knowledge and experience gained on this project are important to the Hanford Site as additional plutonium processing facilities are scheduled for demolition in the near future. Other sites throughout the DOE Complex may also be faced with similar challenges. Numerous innovations and effective work practices were implemented on this project. Accordingly, a series of ''Lessons Learned and Innovative Practices Fact Sheets'' were developed and are included as an appendix to this report. This collection of fact sheets is not intended to capture every innovative work practice and lesson learned, but rather to

Feasibility study of plutonium recycling in light water reactors

International Nuclear Information System (INIS)

Tabuchi, Hideoto

1979-01-01

The feasibility of plutonium recycling in light water reactors has been studied by the Agency of Natural Resources and Energy, MITI. As the first step of the feasibility study, it was planned to charge two fuel assemblies, containing uranium-plutonium mixed oxide (MO 2 ), in the core of the Tsuruga nuclear power plant (BWR) for testing. The design of fuel the safety of these fuel and the operating characteristics of these special fuel assemblies were evaluated. The specifications of MO 2 fuel pin and fuel assembly are compared to those of present uranium oxide (UO 2 ) fuel. The weight of fissile plutonium in one MO 2 fuel assembly is 2.22 kg. The characteristics of MO 2 fuel assemblies, such as reactivity, control rod worth and power distribution can be kept similar to UO 2 fuel. The plutonium isotope ratio of the MO 2 fuel is assumed as that obtained in the fuel taken out of the Tokai No. 1 gas cooled reactor. The temperature distribution in the fuel pellets is shown, compared to that of UO 2 fuel. The linear power density is 440 w/cm at the beginning of the fuel life and 360 w/cm after the burn-up of 44,000 Mwd/t. The stress in the cladding tubes of MO 2 fuel is not different from that of UO 2 fuel. The pellet-cladding interaction (PCM1) was analyzed, utilizing the FEM code, FEAST. Concerning the calculation of resonance absorption, the space dependence of thermal neutron spectra and the nuclear behavior of hollow pellets the methods of design calculation were checked up. It was recognized that regarding the nuclear characteristics of MO 2 fuel, no special technical question remains. (Nakai, Y.)

Bibliography on plutonium and its compounds; Bibliographie sur le plutonium et ses composes

Energy Technology Data Exchange (ETDEWEB)

Dirian, J; Choquet, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1958-07-01

Collection of bibliographical references on plutonium and its principal compounds from 1942 to end of 1957. (author) [French] Compilation de references bibliographiques sur le plutonium et ses principaux composes de 1942 a fin 1957. (auteur)

Plutonium speciation affected by environmental bacteria

International Nuclear Information System (INIS)

Neu, M.P.; Icopini, G.A.; Boukhalfa, H.

2005-01-01

Plutonium has no known biological utility, yet it has the potential to interact with bacterial cellular and extracellular structures that contain metal-binding groups, to interfere with the uptake and utilization of essential elements, and to alter cell metabolism. These interactions can transform plutonium from its most common forms, solid, mineral-adsorbed, or colloidal Pu(IV), to a variety of biogeochemical species that have much different physico-chemical properties. Organic acids that are extruded products of cell metabolism can solubilize plutonium and then enhance its environmental mobility, or in some cases facilitate plutonium transfer into cells. Phosphate- and carboxylate-rich polymers associated with cell walls can bind plutonium to form mobile biocolloids or Pu-laden biofilm/mineral solids. Bacterial membranes, proteins or redox agents can produce strongly reducing electrochemical zones and generate molecular Pu(III/IV) species or oxide particles. Alternatively, they can oxidize plutonium to form soluble Pu(V) or Pu(VI) complexes. This paper reviews research on plutonium-bacteria interactions and closely related studies on the biotransformation of uranium and other metals. (orig.)

Plutonium vulnerability issues at Hanford's Plutonium Finishing Plant

International Nuclear Information System (INIS)

Feldt, E.; Templeton, D.W.; Tholen, E.

1995-01-01

The Plutonium Finishing Plant (PFP) at the Hanford, Washington Site was operated to produce plutonium (Pu) metal and oxide for national defense purposes. Due to the production requirements and methods utilized to meet national needs and the abrupt shutdown of the plant in the late 1980s, the plant was left in a condition that poses a risk of radiation exposure to plant workers, of accidental radioactive material release to the environment, and of radiation exposure to the public. In early 1994, an Environmental Impact Statement (EIS) to determine the best methods for cleaning out and stabilizing Pu materials in the PFP was started. While the EIS is being prepared, a number of immediate actions have been completed or are underway to significantly reduce the greatest hazards in the PFP. Recently, increased attention his been paid to Pu risks at Department of Energy (DOE) facilities resulting in the Department-wide Plutonium Vulnerability Assessment and a recommendation by the Defense Nuclear Facilities Safety Board (DNFSB) for DOE to develop integrated plans for managing its nuclear materials

Results from an interlaboratory exercise on the determination of plutonium isotopic ratios by gamma spectrometry

International Nuclear Information System (INIS)

Ottmar, H.

1981-07-01

Results form interlaboratory comparison measurements on the determination of plutonium isotopic ratios by gamma spectrometry, organized by the ESARDA Working Group on Techniques and Standards for Nondestructive Analysis, are presented and discussed. Nine laboratories from nine countries or international organizations participated in the intercomparison exercise, which included both laboratories' own measurements on the plutonium isotopic reference materials NBS-SRM 946, 947, 948 and comparison analyses of gamma spectra from these materials distributed to the participating laboratories. Results from the intercomparison analyses have been used to reevaluate some gamma branching intensity ratios required for plutonium isotopic ratio measurements. (orig.) [de

Cigarette smoke and plutonium

International Nuclear Information System (INIS)

Filipy, R.E.

1982-01-01

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. Progress was made on two fronts during the past year. The autoradiographic technique developed from detection of plutonium on the interior surface of pulmonary airways (Annual Report, 1978) has been adapted to routine use in examining tracheas and bronchi of rats. Also, dogs exposed to cigarette smoke for over a year after inhalation of plutonium were killed and necropsied

Plutonium inventories for stabilization and stabilized materials

Energy Technology Data Exchange (ETDEWEB)

Williams, A.K.

1996-05-01

The objective of the breakout session was to identify characteristics of materials containing plutonium, the need to stabilize these materials for storage, and plans to accomplish the stabilization activities. All current stabilization activities are driven by the Defense Nuclear Facilities Safety Board Recommendation 94-1 (May 26, 1994) and by the recently completed Plutonium ES&H Vulnerability Assessment (DOE-EH-0415). The Implementation Plan for accomplishing stabilization of plutonium-bearing residues in response to the Recommendation and the Assessment was published by DOE on February 28, 1995. This Implementation Plan (IP) commits to stabilizing problem materials within 3 years, and stabilizing all other materials within 8 years. The IP identifies approximately 20 metric tons of plutonium requiring stabilization and/or repackaging. A further breakdown shows this material to consist of 8.5 metric tons of plutonium metal and alloys, 5.5 metric tons of plutonium as oxide, and 6 metric tons of plutonium as residues. Stabilization of the metal and oxide categories containing greater than 50 weight percent plutonium is covered by DOE Standard {open_quotes}Criteria for Safe Storage of Plutonium Metals and Oxides{close_quotes} December, 1994 (DOE-STD-3013-94). This standard establishes criteria for safe storage of stabilized plutonium metals and oxides for up to 50 years. Each of the DOE sites and contractors with large plutonium inventories has either started or is preparing to start stabilization activities to meet these criteria.

Interference from radon-thoron daughters in plutonium channel of a continuous plutonium-in-air monitor

International Nuclear Information System (INIS)

Pendharkar, K.A.; Krishnamony, S.

1983-01-01

This paper summarises the results of a study conducted to define the extent of interference from the daughter products of radon/thoron to the plutonium channel of a continuous plutonium-in-air monitor. The effect on the detection limits of the instrument due to chemical form (transportable or non-transportable) and isotopic composition of plutonium aerosol are briefly discussed. (author)

Compositions of airborne plutonium-bearing particles from a plutonium finishing operation

International Nuclear Information System (INIS)

Sanders, S.M. Jr.

1976-11-01

The elemental composition of 111 plutonium-bearing particles was determined (using an electron microprobe) as part of a program to investigate the origin and behavior of the long-lived transuranic radionuclides released from fuel reprocessing facilities at the Savannah River Plant. These particles, collected from wet-cabinet and room-air exhausts from the plutonium finishing operation (JB-Line), were between 0.4 and 36 μm in diameter. Ninety-nine of the particles were found to be aggregates of various minerals and metals, six were quartz, and six were small (less than 2-μm-diameter) pieces of iron oxide. Collectively, these particles contained less minerals and more metals than natural dusts contain. The metallic constituents included elements normally not found in dusts, e.g., chromium, nickel, copper, and zinc. Concentrations of aluminum and iron exceeded those normally found in minerals. Elemental concentrations in individual particles covered a wide range: one 2-μm-diameter particle contained 97 percent NiO, a 9-μm-diameter particle contained 72 percent Cr 2 O 3 . Although the particles were selected because they produced plutonium fission tracks, the plutonium concentration was too low to be estimated by microprobe analysis in all but a 1-μm-diameter particle. This plutonium-bearing particle contained 73 percent PuO 2 by weight in combination with Fe 2 O 3 and mica; its activity was estimated at 0.17 pCi of 239 Pu

Plutonium use - present status and perspectives

International Nuclear Information System (INIS)

Dievoet, J. van; Fossoul, E.; Jonckheere, E.; Bemden, E. van den

1977-01-01

Plutonium is being produced in increasing quantities in the so-called proven reactors, which are mostly of the light-water type. Evaluation of this production on a world scale shows that it would be theoretically possible to construct a large number of breeders and thus to make the best use of the intrinsic qualities of plutonium as a fissionable material, while considerably reducing the consumption of uranium. This source of plutonium is nevertheless dependent on an essential stage of the fuel cycle, namely reprocessing of irradiated fuel. The long delays in installing an adequate world reprocessing capacity are substantially weakening the prospects for the introduction of breeders. Furthermore, the critical situation as regards reprocessing may delay the development of complementary reprocessing methods for fuels with a high plutonium content and high burn-up. When it is recalled that fast reactors themselves may suffer some delay in their technological development, if only because of the intention to build power plants of very high unit capacity immediately, it must be concluded that another use will have to be considered for the plutonium available in future -use in thermal reactors, i.e. recycling. The recycling of plutonium is a well-known technique today and the objections which could be raised against it hardly stand up to analysis. Utilization of plutonium offers an appreciable saving in terms of uranium and separative work units, the consumption being of a low order of magnitude in comparison with the total amount of plutonium needed for the eventual fabrication of the first fast reactor cores. It can also be shown that immediate reprocessing of the recycling fuel is not essential for the economics of the concept. Temporary storage of recycled fuel has the advantage of concentrating plutonium in a particularly safe form, namely in irradiated plutonium-bearing fuel assemblies. Lastly, recycling offers such flexibility that it does not in practice represent

Plutonium biokinetics in humans

International Nuclear Information System (INIS)

Popplewell, D.; Ham, G.; McCarthy, W.; Lands, C.

1994-01-01

By using an 'unusual' isotope it is possible to carry out experiments with plutonium in volunteers at minimal radiation dose levels. Measurements have been made of the gut transfer factor and the urinary excretion of plutonium after intravenous injection. (author)

Cigarette smoke and plutonium

International Nuclear Information System (INIS)

Anon.

1981-01-01

The overall objective of this study is to determine whether cigarette smoking increases the probability of plutonium-induced lung cancer. Initial experiments, designed to characterize the effect of chronic cigarette smoke exposure on pulmonary clearance of plutonium aerosols, are described

Polarographic study of the electrochemical properties of plutonium; Etude polarographique des proprietes electrochimiques du plutonium

Energy Technology Data Exchange (ETDEWEB)

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

1968-07-01

The behaviour of the different degrees of oxidation of plutonium have been studied using a falling drop mercury electrode in a non-complexing medium: dilute perchloric acid. In this medium it is possible to carry out the polarographic determination of plutonium using the reduction step situated at - 0.54 V/ECS which corresponds to the passage from the degree of oxidation(V) to the degree(III). The modifications brought about by a complexing ion, acetate, are then observed and interpreted. The existence of two plutonium(IV) acetic complexes has been shown; one is a polymerized substance. (author) [French] Le comportement des differents degres d'oxydation du plutonium est etudie a l'electrode a gouttes de mercure dans un milieu non complexant: l'acide perchlorique dilue. Il est possible dans ce milieu d'effectuer le dosage polarographique du plutonium en utilisant la vague de reduction situee a - 0.54 V/ECS qui correspond au passage du degre d'oxydation(V) au degre(III). Les modifications apportees par un ion complexant, l'acetate, sont ensuite observees et interpretees. Deux complexes acetiques du plutonium(IV) ont ete mis en evidence, dont l'un est un compose polymerise. (auteur)

Comparison of simulated to actual plutonium deposition at the Savannah River Plant

International Nuclear Information System (INIS)

Carlson, D.C.; Garrett, A.J.; Gay, D.D.; Murphy, C.E.; Pinder, J.E. III.

1982-01-01

Minute amounts of plutonium are released from the Savannah River Plant (SRP) separations facilities and deposited in the surrounding environs. Long-term deposition measurements show that contributions to offsite environmental plutonium by the SRP are negligible compared to fallout from weapons tests. The Savannah River Laboratory (SRL) recently developed a deposition model and compared its predictions to the observed plutonium deposition pattern. The model reproduced the observed range of deposition rates when full and truncated lognormal distributions of particle sizes were used to represent the emissions. Model predictions of total deposition out to 30 km were low by about a factor of two relative to estimates based on integrations of the empirical deposition curves. More measurements are planned, which should reduce uncertainties about model assumptions and the observed deposition rates

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)

A World made of Plutonium?

International Nuclear Information System (INIS)

Broda, E.

1976-01-01

This lecture by Engelbert Broda was written for the 26th Pugwash Conference in Mühlhausen, Germany, 26 – 31 August 1976: Public doubts about nuclear energy are generally directed at the problems of routine emissions of radionuclides, of catastrophic accidents, and of terminal waste disposal. Curiously, the most important problem is not being given sufficient attention: The use of plutonium from civilian reactors fpr weapons production. According to current ideas about a nuclear future, 5000 tons (order of magnitude) of plutonium are to be made annually by year 2000, and about 10 000 tons will all the time be in circulation (transport, reprocessing, reproduction of fuel elements, etc.). It is a misconception that plutonium from power reactors is unsuitable as a nuclear explosive. 5000 tons are enough for several hundred thousand (!) of bombs, Nagasaki type. By the year 2000 maybe 40 – 50 countries will have home-made plutonium. Plutonium production and proliferation are the most serious problems in a nuclear world. (author)

Using Biomolecules to Separate Plutonium

Science.gov (United States)

Gogolski, Jarrod

Used nuclear fuel has traditionally been treated through chemical separations of the radionuclides for recycle or disposal. This research considers a biological approach to such separations based on a series of complex and interdependent interactions that occur naturally in the human body with plutonium. These biological interactions are mediated by the proteins serum transferrin and the transferrin receptor. Transferrin to plutonium in vivo and can deposit plutonium into cells after interacting with the transferrin receptor protein at the cell surface. Using cerium as a non-radioactive surrogate for plutonium, it was found that cerium(IV) required multiple synergistic anions to bind in the N-lobe of the bilobal transferrin protein, creating a conformation of the cerium-loaded protein that would be unable to interact with the transferrin receptor protein to achieve a separation. The behavior of cerium binding to transferrin has contributed to understanding how plutonium(IV)-transferrin interacts in vivo and in biological separations.

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)

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

Technological alternatives for plutonium transport

International Nuclear Information System (INIS)

1978-12-01

This paper considers alternative transport modes (air, sea, road, rail) for moving (1) plutonium from a reprocessing plant to a store or a fuel fabrication facility, and (2) MOX fuel from the latter to a reactor. These transport modes and differing forms of plutonium are considered in terms of: their proliferation resistance and safeguards; environmental and safety aspects; and economic aspects. It is tentatively proposed that the transport of plutonium could continue by air or sea where long distances are involved and by road or rail over shorter distances; this would be acceptable from the non-proliferation, environmental impact and economic aspects - there may be advantages in protection if plutonium is transported in the form of mixed oxide

Gamma spectrometric methods for measuring plutonium

International Nuclear Information System (INIS)

Gunnink, R.

1978-01-01

Nondestructive analyses of plutonium can be made by detecting and measuring the gamma rays emitted by a sample. Although qualitative and semiquantitative assays can be performed with relative ease, only recently have methods been developed, using computer analysis techniques, that provide quantitative results. This paper reviews some new techniques developed for measuring plutonium. The features of plutonium gamma-ray spectra are reviewed and some of the computer methods used for spectrum analysis are discussed. The discussion includes a description of a powerful computer method of unfolding complex peak multiplets that uses the standard linear least-squares techniques of data analysis. This computer method is based on the generation of response profiles for the isotopes composing a plutonium sample and requires a description of the peak positions, relative intensities, and line shapes. The principles that plutonium isotopic measurements are based on are also developed, followed by illustrations of the measurement procedures as applied to the quantitative analysis of plutonium liquid and solid samples

Plutonium

Energy Technology Data Exchange (ETDEWEB)

Miner, William N

1964-01-01

This pamphlet discusses plutonium from discovery to its production, separation, properties, fabrication, handling, and uses, including use as a reactor fuel and use in isotope power generators and neutron sources.

Plutonium Vulnerability Management Plan

International Nuclear Information System (INIS)

1995-03-01

This Plutonium Vulnerability Management Plan describes the Department of Energy's response to the vulnerabilities identified in the Plutonium Working Group Report which are a result of the cessation of nuclear weapons production. The responses contained in this document are only part of an overall, coordinated approach designed to enable the Department to accelerate conversion of all nuclear materials, including plutonium, to forms suitable for safe, interim storage. The overall actions being taken are discussed in detail in the Department's Implementation Plan in response to the Defense Nuclear Facilities Safety Board (DNFSB) Recommendation 94-1. This is included as Attachment 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

Economic assumptions for evaluating reactor-related options for managing plutonium

International Nuclear Information System (INIS)

Rothwell, G.

1996-01-01

This paper discusses the economic assumptions in the U.S. National Academy of Sciences' report, Management and Disposition of Excess Weapons Plutonium: Reactor-Related Options (1995). It reviews the Net Present Value approach for discounting and comparing the costs and benefits of reactor-related options. It argues that because risks associated with the returns to plutonium management are unlikely to be constant over time, it is preferable to use a real risk-free rate to discount cash flows and explicitly describe the probability distributions for costs and benefits, allowing decision makers to determine the risk premium of each option. As a baseline for comparison, it assumes that one economic benefit of changing the current plutonium management system is a reduction in on-going Surveillance and Maintenance (S and M) costs. This reduction in the present value of S and M costs can be compared with the discounted costs of each option. These costs include direct construction costs, indirect costs, operating costs minus revenues, and decontamination and decommissioning expenses. The paper also discusses how to conduct an uncertainty analysis. It finishes by summarizing conclusions and recommendations and discusses how these recommendations might apply to the evaluation of Russian plutonium management options. (author)

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)

The significance of liver in metabolism of plutonium 239

International Nuclear Information System (INIS)

Netchev, Christo.

1977-01-01

Plutonium 239 has an important toxicological significance and is widely used in the nuclear industry which makes the study of its metabolism in the organism appear of substantial interest. The role of the liver in the distribution of radionuclide and its barrier capabilities, determining to a certain extent the back transport of the isotope from the blood plasma into the gut is studied. The storage of Plutonium 239 in the organ and its reexcretion by way of the gull is quantitatively demonstrated. This question is related to the exact determination of the coefficient of absorption of the radioisotope in the digestive tract. The radionuclide is inserted into organism as PuCl 3 directly into vein jugularis and vein portae. The peculiarities of its distribution in the liver by the two ways of introduction as well as the essential differences in the radioactivity of the products of excretion by portal application are described. The mechanism of the storage of the radioisotope in the organ is explained to a great extent with its physical and chemical condition in the liver tissue. Plutonium 239 is found in the liver completely as a complex compound with the tissue proteins, the combining with globulines predominating. The dynamics of exchange of the radionuclide in the organ is determined mainly by its complex combination with the globulins. The part of nuclide connected with the other protein fractions of liver is not significant and hence they do not much influence kinetics in the organ

Prospects for the Use of Plutonium in Reactors; Prospective d'Utilisation du Plutonium dans les Reacteurs

Energy Technology Data Exchange (ETDEWEB)

Fossoul, E.; Haubert, P. [BELGONUCLEAIRE (Belgium); Hirschberg, D.; Morlet, E. [International Business Machines of Belgium, Bruxelles (Belgium)

1967-09-15

The introduction, at an increasing rate, of power reactors using slightly enriched uranium will inevitably lead to the production of considerable quantities of plutonium over the next decade. Fast reactors will not be capable of absorbing this material before 1980. The question thus arises of whether one should store the plutonium far future use in fast reactors, recycle it in existing thermal reactors, or try to sell it. The problem has been studied for an electric power generating system that does not foresee selling the plutonium produced by its reactors and does not buy plutonium outside, which enables a good approximation to be made and eliminates the major unknown quantity represented by the future market price of plutonium. Assuming within this system a programme that provides for the construction of power reactors of a given type and capacity at specific dates, the utilization of the plutonium produced can be optimized by linear programming techniques so as to minimize the discounted total cost of the power generated over a given period. A later stage consists in optimizing, by various techniques, not only the utilization but also the production of plutonium by appropriate selection of the power reactor types to be constructed. (author) [French] L'implantation, a un rythme croissant, de centrales nucleaires a uranium legerement enrichi entrainera la production ineluctable d'une quantite importante de plutonium au cours de la prochaine decennie. Les reacteurs a neutrons rapides ne seront capables d'absorber cette production qu'apres 1980. La question se pose donc de savoir s'il est preferable de stocker le plutonium en vue de son utilisation ulterieure dans les reacteurs a neutrons rapides plutot que de le recycler dans les reacteurs actuels a neutrons thermiques ou d'essayer de le vendre. Ce probleme a ete etudie dans le cadre d'un systeme de production d'energie electrique qui ne prevoirait pas la vente du plutonium produit par ses reacteurs nucleaires ni

Radiological safety aspects of handling plutonium

International Nuclear Information System (INIS)

Sundararajan, A.R.

2016-01-01

Department of Atomic Energy in its scheme of harnessing the nuclear energy for electrical power generation and strategic applications has given a huge role to utilization of plutonium. In the power production programme, fast reactors with plutonium as fuel are expected to play a major role. This would require establishing fuel reprocessing plants to handle both thermal and fast reactor fuels. So in the nuclear fuel cycle facilities variety of chemical, metallurgical, mechanical operations have to be carried out involving significant inventories of "2"3"9 Pu and associated radionuclides. Plutonium is the most radiotoxic radionuclide and therefore any facility handling it has to be designed and operated with utmost care. Two problems of major concern in the protection of persons working in plutonium handling facilities are the internal exposure to the operating personnel from uptake of plutonium and transplutonic nuclides as they are highly radiotoxic and the radiation exposure of hands and eye lens during fuel fabrication operations especially while handling recycled high burn up plutonium. In view of the fact that annual limit for intake is very small for "2"3"9Pu and its radiation emission characteristics are such that it is a huge challenge for the health physicists to detect Pu in air and in workers. This paper discusses the principles and practices followed in providing radiological surveillance to workers in plutonium handling areas. The challenges in protecting the workers from receiving exposures to hands and eye lens in handling high burn up plutonium are also discussed. The sites having Pu fuel cycle facilities should have trained medical staff to handle cases involving excessive intake of plutonium. (author)

Documentation of acceptable knowledge for Los Alamos National Laboratory Plutonium Facility TRU waste stream

International Nuclear Information System (INIS)

Montoya, A.J.; Gruetzmacher, K.M.; Foxx, C.L.; Rogers, P.Z.

1998-03-01

Characterization of transuranic waste from the LANL Plutonium Facility for certification and transportation to WIPP includes the use of acceptable knowledge as specified in the WIPP Quality Assurance Program Plan. In accordance with a site specific procedure, documentation of acceptable knowledge for retrievably stored and currently generated transuranic waste streams is in progress at LANL. A summary overview of the TRU waste inventory is complete and documented in the Sampling Plan. This document also includes projected waste generation, facility missions, waste generation processes, flow diagrams, times, and material inputs. The second part of acceptable knowledge documentation consists of assembling more detailed acceptable knowledge information into auditable records and is expected to require several years to complete. These records for each waste stream must support final assignment of waste matrix parameters, EPA hazardous waste numbers, and radionuclide characterization. They must also include a determination whether waste streams are defense waste streams for compliance with the WIPP Land Withdrawal Act. The LANL Plutonium Facility's mission is primarily plutonium processing in basic special nuclear material (SNM) research activities to support national defense and energy programs. It currently has about 100 processes ranging from SNM recovery from residues to development of plutonium 238 heat sources for space applications. Its challenge is to characterize and certify waste streams from such diverse and dynamic operations using acceptable knowledge. This paper reports the progress on the certification of the first of these waste streams to the WIPP WAC

Effects of plutonium redistribution on lung counting

International Nuclear Information System (INIS)

Swinth, K.L.

1976-01-01

Early counts of Pu deposition in lungs will tend to overestimate lung contents since calibrations are performed with a uniform distribution and since a more favorable geometry exists in contaminated subjects because the activity is closer to the periphery of the lungs. Although the concentration into the outer regions of the lungs continues as evidenced by the autopsy studies, the counts performed by L X-rays will probably underestimate the lung content; because, simplistically, the geometry several years after exposure consists of a spherical shell with a point of activity in the center. This point of activity represents concentration in the lymph nodes from which the 60 keV gamma of 241 Am will be counted, but from which few of the L X-rays will be counted (this is an example of interorgan distribution). When a correction is made to the L X-ray intensity, the lymph node contribution will tend to increase the amount subtracted while correcting for 241 Am X-rays. It is doubtful that the relative increase in X-ray intensity by concentration in the pleural and sub-pleural regions will compensate for this effect. This will make the plutonium burden disappear while the 241 Am can still be detected. This effect has been observed in a case where counts with an intraesophageal probe indicated a substantial lymph node burden. In order to improve the accuracy of in vivo plutonium measurements, an improved understanding of pulmonary distribution and of distribution effects on in vivo counting are required

Plutonium-induced lymphadenitis in beagles

International Nuclear Information System (INIS)

Dagle, G.E.; Park, J.F.

1976-01-01

Plutonium oxide particles accumulate in the tracheobronchial lymph nodes of beagles exposed by inhalation and in the popliteal lymph nodes after subcutaneous injection in the hind paws. The sequence of histopathologic changes after phagocytosis of particles included necrosis, increased numbers of macrophages, and fibroplasia. Scar tissue eventually replaced the normal architecture of the lymph nodes and sequestered the plutonium particles from surrounding parenchyma. Electron microscopy showed that plutonium particles were aggregated in phagolysosomes of macrophages

Guidelines for international plutonium management: Overview and implications

International Nuclear Information System (INIS)

Bryson, M.C.; Fitzgerald, C.P.; Kincaid, C.

1998-01-01

In September, 1997, nine of the world's plutonium-using countries agreed to a set of guidelines for international plutonium management, with acceptances to be submitted to the International Atomic Energy Agency on December 1. Following three years of discussion, the guidelines provide a unified package of accepted rules for the storage, handling, and transportation of civil plutonium as well as military plutonium that has been declared as no longer required for defense purposes. New requirements include a formal declaration of national plutonium strategies, which will recognize the environmental, economic, and proliferation concerns and the consequent importance of balancing plutonium supply and demand. Nations will also make annual declaration of their non-military stockpiles of unirradiated plutonium, together with estimates of the plutonium content in spent reactor fuel. These guidelines represent the first formally accepted recognition of the need for plutonium management of this scope and could thus provide a partial basis for future monitoring and policy regimes

Observations of the distribution and the nature of alpha-active particulate material in a HEPA filter used for plutonium-containing dust

International Nuclear Information System (INIS)

Ryan, M.T.; McDowell, W.J.

1977-02-01

Autoradiography has been used to determine the distribution and the nature of plutonium particulate material on a high-efficiency particulate air (HEPA) filter used to filter 239 Pu-containing dust. Higher concentrations of alpha-active material on upstream and downstream folds of the filter indicate uneven airflow through the filter. Observations of aggregate recoil particles on the downstream face of the filter suggest that aggregate recoil transfer, a mechanism which may reduce long-term HEPA filter efficiency, may be occurring. Amounts of alpha activity found on downstream filters confirm this supposition

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

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

Dissolution of uranium and plutonium particles: simulations using the Mercer equation

International Nuclear Information System (INIS)

Cowan, C.E.; Jenne, E.A.

1983-10-01

There is a need to be able to predict the amount of plutonium that will be in solution at a given time from dissolution of particles in order to better predict the environmental behavior and possible adverse effects of plutonium spills. The equation developed by Mercer (1967) to simulate the dissolution of particles in lungs was parameterized and used to simulate the dissolution of a population of plutonium or uranium particles in the soil. Parameter values for the size distribution of particles in soil, and the density of the particles were found; however, values for the shape factors, and the dissolution rate were virtually non-existent. The calculated mass dissolved was most sensitive to the median diameter of the population of particles and least sensitive to the geometric standard deviation. A given percent change in the shape parameter and the dissolution rate resulted in approximately an equal percent change in the mass dissolved. Provided that the population of particles follows a log-normal distribution, the particles are homogeneous in composition and the dissolution can be represented by first-order kinetics, this equation can probably be applied with slight modification to estimate the mass dissolved at a given time. 66 references, 7 figures, 4 tables

Plutonium story

International Nuclear Information System (INIS)

Seaborg, G.T.

1981-09-01

The first nuclear synthesis and identification (i.e., the discovery) of the synthetic transuranium element plutonium (isotope 238 Pu) and the demonstration of its fissionability with slow neutrons (isotope 239 Pu) took place at the University of California, Berkeley, through the use of the 60-inch and 37-inch cyclotrons, in late 1940 and early 1941. This led to the development of industrial scale methods in secret work centered at the University of Chicago's Metallurgical Laboratory and the application of these methods to industrial scale production, at manufacturing plants in Tennessee and Washington, during the World War II years 1942 to 1945. The chemical properties of plutonium, needed to devise the procedures for its industrial scale production, were studied by tracer and ultramicrochemical methods during this period on an extraordinarily urgent basis. This work, and subsequent investigations on a worldwide basis, have made the properties of plutonium very well known. Its well studied electronic structure and chemical properties give it a very interesting position in the actinide series of inner transition elements

Accumulation of plutonium from fallout in southern Finns and Lapps

International Nuclear Information System (INIS)

Mussalo-Rauhamaa, H.

1981-01-01

The body burden of 239 , 240 Pu and 238 Pu from fallout in southern Finns and Lapps was determined by ion exchange and alpha-spectrometry through analyses of autopsy tissue samples. Comparing the body burden against the inhalation and ingestion intake of plutonium of these population groups the fractional absorption factor for plutonium from the human gastrointestinal tract and lungs was estinated. In addition, the determined tissue values were compared with those computed with the aid of the ICRP lung model and plutonium content of surface air in the Helsinki area. The 239 , 240 Pu concentrations per wet weight of tissue descended in the order liver>lymph nodes>bone>lung>testes>muscle. A dependence of plutonium content of tissues on the amount of air inhaled by the person during the fallout period and, thus, on the age of the person, was shown. The skeletal distribution of plutonium in man was roughly similar to that reported for animals. The ratio of 239 , 240 Pu content in vertebrae to that in ribs was 1.4, on the average, and the rib/femur ratio 1.0. The average body burden of 239 , 240 Pu in adult southern Finn and Lapp males was estimated to be 1.2 pCi (44.4 mBq), of which about 51 per cent was located in liver and 40 per cent in skeleton. The estimates for the ingestion and inhalation intake of 239 , 240 Pu during the period 1945-78 were 36 and 18 pCi (1.3, 0.67 Bq) and 540 and 13 pCi (19.9, 0.48 Bq) for southern Finn and Lapp males, respectively. The estimated fractional absorption factor of plutonium in humn GI-tract was of the order (6-9)x10 -4 and in lungs (7.5-8.5)x10 -2 . (author)

Plutonium research and related activities at the Amarillo National Resource Center for Plutonium

International Nuclear Information System (INIS)

Hartley, R.S.; Beard, C.A.; Barnes, D.L.

1998-01-01

With the end of the Cold War, the US and Russia are reducing their nuclear weapons stockpiles. What to do with the materials from thousands of excess nuclear weapons is an important international challenge. How to handle the remaining US stockpile to ensure safe storage and reliability, in light of the aging support infrastructure, is an important national challenge. To help address these challenges and related issues, the Amarillo National Resource Center for Plutonium is working on behalf of the State of Texas with the US Department of Energy (DOE). The center directs three major programs that address the key aspects of the plutonium management issue: (1) the Communications, Education, Training and Community Involvement Program, which focuses on informing the public about plutonium and providing technical education at all levels; (2) the Environmental, Safety, and Health (ES and H) Program, which investigates the key ES and H impacts of activities related to the DOE weapons complex in Texas; and (3) the Nuclear and Other Materials Program, which is aimed at minimizing safety and proliferation risks by helping to develop and advocate safe stewardship, storage, and disposition of nuclear weapons materials. This paper provides an overview of the center's nuclear activities described in four broad categories of international activities, materials safety, plutonium storage, and plutonium disposition

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

Bayesian methods for interpreting plutonium urinalysis data

International Nuclear Information System (INIS)

Miller, G.; Inkret, W.C.

1995-01-01

The authors discuss an internal dosimetry problem, where measurements of plutonium in urine are used to calculate radiation doses. The authors have developed an algorithm using the MAXENT method. The method gives reasonable results, however the role of the entropy prior distribution is to effectively fit the urine data using intakes occurring close in time to each measured urine result, which is unrealistic. A better approximation for the actual prior is the log-normal distribution; however, with the log-normal distribution another calculational approach must be used. Instead of calculating the most probable values, they turn to calculating expectation values directly from the posterior probability, which is feasible for a small number of intakes

PRISM reactor. An option for plutonium disposition?

Energy Technology Data Exchange (ETDEWEB)

Fehlinger, Sebastian; Friess, Friederike; Kuett, Moritz [IANUS, Technische Universitaet Darmstadt (Germany)

2015-07-01

The Power Reactor Innovative Small Module (PRISM) is sodium cooled fast reactor model. The energy output depends on the core configuration, however with an energy output of approximately 300 MWe, the PRISM reactor belongs to the class of small modular reactors. Beside using the reactor as a breeder reactor or for the transmutation of nuclear waste, it might also be used as a burner reactor for separated plutonium. This includes for example U.S.-American excess weapon-grade plutonium as well as separated reactor-grade plutonium. Recently, there has been an ongoing discussion in GB to use the PRISM reactor to dispose their excess civilian plutonium. Depending on the task, the core configuration varies slightly. We will present different layouts and the matching MCNP models, these models can then be used to conduct depletion calculations. From these results, analysis of the change in the plutonium isotopics in the spent fuel, the amount of fissioned plutonium, and the possible annual plutonium throughputs is possible.

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.)

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

Plutonium production and utilization forecasts in Europe

International Nuclear Information System (INIS)

Haijtink, B.

1976-01-01

The planned accelerated growth of nuclear energy generation in the near future will lead to a large production of plutonium in the thermal reactors. Therefore, up to 1985, the major part of the available plutonium will be plutonium recovered from spent uranium-metal, particularly in the United Kingdom and in France. Because of the low demand for fuelling the fast breeder reactors within the near future, a surplus of fissile plutonium will be accumulated in Europe. Even if the planned availability of the oxide reprocessing capacity will be delayed with two or three years, a plutonium surplus will still exist in Europe, e.g.; in 1985: 25-20 tons. On longer term, up to 2000, the plutonium production in thermal reactors will be sufficient to meet the estimated demand for fast breeder reactors at their commercial introduction foreseen for the nineties. That means that all the plutonium surplus needs not to be stocked for use in fast breeder reactors later on but could be recycled in thermal reactors. The magnitude of the available fissionable materials give an idea of the importance to promote, on an industrial scale, the plutonium recycling technology

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 titration by controlled potential coulometry; Dosage du plutonium par coulometrie a potentiel impose

Energy Technology Data Exchange (ETDEWEB)

Leguay, N.

2011-07-01

The LAMMAN (Nuclear Materials Metrology Laboratory) is the support laboratory of the CETAMA (Analytical Method Committee), whose two main activities are developing analytic methods, and making and characterizing reference materials. The LAMMAN chose to develop the controlled potential coulometry because it is a very accurate analytical technique which allows the connection between the quantity of element electrolysed to the quantity of electricity measured thanks to the Faraday's law: it does not require the use of a chemical standard. This method was first used for the plutonium titration and was developed in the Materials Analysis and Metrology Laboratory (LAMM), for upgrading its performances and developing it to the titration of other actinides. The equipment and the material used were developed to allow the work in confined atmosphere (in a glove box), with all the restrictions involved. Plutonium standard solutions are used to qualify the method, and in particular to do titrations with an uncertainty better than 0.1 %. The present study allowed making a bibliographic research about controlled potential coulometry applied to the actinides (plutonium, uranium, neptunium, americium and curium). A full procedure was written to set all the steps of plutonium titration, from the preparation of samples to equipments storage. A method validation was done to check the full procedure, and the experimental conditions: working range, uncertainty, performance... Coulometric titration of the plutonium from pure solution (without interfering elements) was developed to the coulometric titration of the plutonium in presence of uranium, which allows to do accurate analyses for the analyses of some parts of the reprocessing of the spent nuclear fuel. The possibility of developing this method to other actinides than plutonium was highlighted thanks to voltammetric studies, like the coulometric titration of uranium with a working carbon electrode in sulphuric medium. (author)

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.

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

Civil plutonium amounts in the world

International Nuclear Information System (INIS)

Naudet, G.

1994-01-01

The experience of plutonium reprocessing in water reactors is positive and today the use of this nuclear fuel is at industrial level. Plutonium quantities in spent fuel go on increasing, plutonium stock coming from reprocessing can be controlled: according to conjuncture, it will evolve by stabilization or decreasing at the beginning of next century

Neutronics benchmark of a MOX assembly with near-weapons-grade plutonium

International Nuclear Information System (INIS)

Difilippo, F.C.; Fisher, S.E.

1998-01-01

One of the proposed ways to dispose of surplus weapons-grade plutonium (Pu) is to irradiate the high-fissile material in light-water reactors in order to reduce the Pu enrichment to the level of spent fuels from commercial reactors. Considerable experience has been accumulated about the behavior of mixed-oxide (MOX) uranium and plutonium fuels for plutonium recycling in commercial reactors, but the experience is related to Pu enrichments typical of spent fuels quite below the values of weapons-grade plutonium. Important decisions related to the kind of reactors to be used for the disposition of the plutonium are going to be based on calculations, so the validation of computational algorithms related to all aspects of the fuel cycle (power distributions, isotopics as function of the burnup, etc.), for weapons-grade isotopics is very important. Analysis of public domain data reveals that the cycle-2 irradiation in the Quad cities boiling-water reactor (BWR) is the most recent US destructive examination. This effort involved the irradiation of five MOX assemblies using 80 and 90% fissile plutonium. These benchmark data were gathered by General Electric under the sponsorship of the Electric Power Research Institute. It is emphasized, however, that global parameters are not the focus of this benchmark, since the five bundles containing MOX fuels did not significantly affect the overall core performance. However, since the primary objective of this work is to compare against measured post-irradiation assembly data, the term benchmark is applied here. One important reason for performing the benchmark on Quad Cities irradiation is that the fissile blends (up to 90%) are higher than reactor-grade and, quite close to, weapons-grade isotopics

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

Concentration and vertical distribution of plutonium and americium in Italian mosses and lichens

International Nuclear Information System (INIS)

Jia, G.; Desideri, D.; Guerra, F.; Meli, M.A.; Testa, C.

1997-01-01

The plutonium and americium concentration and vertical distribution in some Italian mosses and lichens have been determined. The 239,240 Pu, 238 Pu and 241 Am concentration ranges in tree trunk lichens 0.83-1.87, 0.052-0.154 and 0.180-0.770 Bq/kg, respectively. The corresponding values in tree mosses are higher and more scattered ranging from 0.321 to 4.96, from 0.029 to 0.171 and from 0.200 to 1.93 Bq/kg. The mean 238 Pu/ 239,240 Pu and 241 Am/ 239,240 Pu ratios are 0.088±0.037 and 0.38 ± 0.13 in lichens and 0.091±0.072 and 0.54±0.16 in tree mosses. The Pu and Am concentrations are relatively low in terrestrial mosses. The 239,240 Pu, 238 Pu and 241 Am vertical distributions in a terrestrial moss core (Neckera Crispa) collected near Urbino (central Italy) show an exponential decrease with the height. On the contrary the 241 Am vertical distribution in another terrestrial moss core (Sphagnum Compactum) collected in the Alps (northern Italy) shows an interesting peak at 16 cm which corresponds to the deposition of fallout from the nuclear weapon tests in 1960's. The 241 Am movement upward and downward in the moss core is also studied. The results show once again that both mosses and lichens are very effective accumulators of Pu and Am and that they can be used as good biological indicators of the radionuclide airborne pollution from nuclear facilities and nuclear weapon tests. They can play a very important role in cycling naturally or artificially enhanced radionuclides in the atmosphere over long time scales. (author)

Method of stripping plutonium from tributyl phosphate solution which contains dibutyl phosphate-plutonium stable complexes

International Nuclear Information System (INIS)

Ochsenfeld, W.; Schmieder, H.

1976-01-01

Fast breeder fuel elements which have been highly burnt-up are reprocessed by extracting uranium and plutonium into an organic solution containing tributyl phosphate. The tributyl phosphate degenerates at least partially into dibutyl phosphate and monobutyl phosphate, which form stable complexes with tetravalent plutonium in the organic solution. This tetravalent plutonium is released from its complexed state and stripped into aqueous phase by contacting the organic solution with an aqueous phase containing tetravalent uranium. 6 claims, 1 drawing figure

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

Specification analysis of plutonium fuels : a potentiometric method for the determination of plutonium

International Nuclear Information System (INIS)

Vaidyanathan, S.; Natarajan, P.R.

1977-01-01

A potentiometric method for the routine determination of plutonium in the specification analysis of plutonium fuels is described. Plutonium is oxidized to Pu(VI) with AgO and Pu(VI) is reduced with Fe(II) after the destruction of excess AgO with sulphamic acid. The excess Fe(II) is titrated potentiometrically against K 2 Cr 2 O 7 , the titration being carried out by adding a concentrated titrant solution from a weight burette and a suitably diluted solution from another weight burette near the end. The overall relative standard deviation obtained in 326 analyses of a working standard solution by eight experimenters is 0.14 percent. (author)

Alternative technical summary report for direct disposition in deep boreholes: Direct disposal of plutonium metal/plutonium dioxide in compound canisters, Version 4.0. Fissile Materials Disposition Program

Energy Technology Data Exchange (ETDEWEB)

Wijesinghe, A.M.

1996-08-23

This report summarizes and compares the Immobilized and Direct Beep Borehole Disposition Alternatives. The important design concepts, facility features and operational procedures are briefly described, and a discussion of the issues that affect the evaluation of each alternative against the programmatic assessment criteria that have been established for selecting the preferred alternatives for plutonium disposition.

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)

Electrochemistry of plutonium in molten halides

International Nuclear Information System (INIS)

McCurry, L.E.; Moy, G.M.M.; Bowersox, D.F.

1987-01-01

The electrochemistry of plutonium in molten halides is of technological importance as a method of purification of plutonium. Previous authors have reported that plutonium can be purified by electrorefining impure plutonium in various molten haldies. Work to eluciate the mechanism of the plutonium reduction in molten halides has been limited to a chronopotentiometric study in LiCl-KCl. Potentiometric studies have been carried out to determine the standard reduction potential for the plutonium (III) couple in various molten alkali metal halides. Initial cyclic voltammetric experiments were performed in molten KCL at 1100 K. A silver/silver chloride (10 mole %) in equimolar NaCl-KCl was used as a reference electrode. Working and counter electrodes were tungsten. The cell components and melt were contained in a quartz crucible. Background cyclic voltammograms of the KCl melt at the tungsten electrode showed no evidence of electroactive impurities in the melt. Plutonium was added to the melt as PuCl/sub 3/, which was prepared by chlorination of the oxide. At low concentrations of PuCl/sub 3/ in the melt (0.01-0.03 molar), no reduction wave due to the reduction of Pu(III) was observed in the voltammograms up to the potassium reduction limit of the melt. However on scan reversal after scanning into the potassium reduction limit a new oxidation wave was observed

The Plutonium Temperature Effect Experimental Program

Energy Technology Data Exchange (ETDEWEB)

Haeck, Wim; Leclaire, Nicolas; Letang, Eric [IRSN, Fontenay-aux-Roses (France); Girault, Emmanuel; Fouillaud, Patrick [CEA, VALDUC (France)

2008-07-01

Various theoretical studies have shown that highly diluted plutonium solutions could have a positive temperature effect but (up to now) no experimental program has confirmed this effect. The main goal of the French Plutonium Temperature Effect Experimental Program (or PU+ in short) is to effectively show that such a positive temperature effect exists for diluted plutonium solutions. The experiments were conducted in the 'Apparatus B' facility at the CEA Valduc research centre in France and involved several sub-critical approach type of experiments using plutonium nitrate solutions with concentrations of 14.3, 15 and 20 g/l at temperatures ranging from 20 to 40 deg. C. A total number of 14 phase I experiments (consisting of independent subcritical approaches) have been performed (5 at 20 g/l, 4 at 15 g/l and 5 at 14.3 g/l) between 2006 and 2007. The impact of the uncertainties on the solution acidity and the plutonium concentration makes it difficult to clearly demonstrate the positive temperature effect, requiring an additional phase II experiment (in which the use of the same plutonium solution was ensured) from 22 to 28 deg. C performed in July 2007. This experiment has shown the existence of a positive temperature effect approx +2 pcm/deg. C (from 22 to 28 deg. C for a plutonium concentration of 14.3 g/l). (authors)

Plutonium Speciation, Solubilization and Migration in Soils

International Nuclear Information System (INIS)

Neu, M.; Runde, W.

1999-01-01

This report summarizes research completed in the first half of a three-year project. As outlined in the authors' proposal they are focusing on (1) characterizing the plutonium at an actinide contaminated site, RFETS, including determining the origin, dispersion, and speciation of the plutonium, (2) studying environmentally important plutonium complexes, primarily hydroxides and carbonates, and (3) examining the interactions of plutonium species with manganese minerals. In the first year the authors focused on site based studies. This year they continue to characterize samples from the RFETS, study the formation and structural and spectroscopic features of environmentally relevant Pu species, and begin modeling the environmental behavior of plutonium

Recent trends of plutonium facilities and their control

Energy Technology Data Exchange (ETDEWEB)

Muto, T [Power Reactor and Nuclear Fuel Development Corp., Tokai, Ibaraki (Japan). Tokai Works

1974-02-01

Much interest has been focussed on Pu recycle since the oil crisis because of an expected shortage of enriched uranium. Plutonium handling techniques and plutonium fuel fabricating facilities should be developed to meet the future demand of plutonium, but the radioactive property of plutonium to be reprocessed from spent fuel and recycled plutonium is remarkably different, and it has to be handled safely. Technical criteria for plutonium facilities are specified in the USAEC regulatory guides and other rules. Some of these criteria are location condition, quality of confinement, protection against accidents and so on. The control conditions for plutonium facilities are exposure control, criticality control, measurement control and new system of safeguard. These problems are under development to meet the future requirement for the safe handling of Pu material.

Plutonium Oxide Process Capability Work Plan

Energy Technology Data Exchange (ETDEWEB)

Meier, David E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Tingey, Joel M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2014-02-28

Pacific Northwest National Laboratory (PNNL) has been tasked to develop a Pilot-scale Plutonium-oxide Processing Unit (P3U) providing a flexible capability to produce 200g (Pu basis) samples of plutonium oxide using different chemical processes for use in identifying and validating nuclear forensics signatures associated with plutonium production. Materials produced can also be used as exercise and reference materials.

Qualification criteria to certify a package for air transport of plutonium

International Nuclear Information System (INIS)

1977-12-01

The document describes qualification criteria developed by the U.S. Nuclear Regulatory Commission to certify a package for air transport of plutonium. Included in the document is a discussion of aircraft accident conditions and a summary of the technical basis for the qualification criteria. The criteria require prototype packages to be subjected to various individual and sequential tests that simulate the conditions produced in severe aircraft accidents. Specific post-test acceptance standards are prescribed for each of the three safety functions of a package. The qualification criteria also prescribe certain operational controls to be exercised during transport

Effect of change in diet on excretion of plutonium-239 from organism

International Nuclear Information System (INIS)

Ivanova, N.P.

1987-01-01

To check supposition on milk effect on plutonium-239 excretion from organism the portable water for rats, contained in individual metabolic cages permitting separate excretion analysis, was replaced by milk. Some days later milk was excluded from diet. 24-hourly rate of radionuclide with feces and urine excretion from organism was determined. On the basis of preliminary data analysis it is supposed that interaction of some milk components with biocomponents of blood and deposition organ tissues violate 239 Pu steady equilibrium distribution in organism, affecting its metabolism through the intermediary of blood system. It results in increased plutonium excretion

Long time contamination from plutonium

International Nuclear Information System (INIS)

Fueloep, M.; Patzeltova, N.; Ragan, P.; Matel, L.

1995-01-01

Plutonium isotopes in the organism of the patient (who had participated in the liquidation works after the Chernobyl accident; for three month he had stayed in the epicenter, where he acted as a chauffeur driving a radioactive material to the place of destination) from urine were determined. For determination of the concentration of Pu-239, Pu-240 in urine a modified radiochemical method was used. After mineralization the sample was separated as an anion-nitrate complex with contact by the anion form of the resin in the column. The resin was washed by 8 M HNO 3 , the 8 M HCl with 0.3 M HNO 3 for removing the other radionuclides. The solution 0.36 M HCl with 0.01 M HF was used for the elution of plutonium. Using the lanthanum fluoride technique the sample was filtrated through a membrane filter. The plutonium was detected in the dry sample. The Pu-239 tracer was used for the evaluation of the plutonium separation efficiency. The alpha spectrometric measurements were carried out with a large area silicon detector. The samples were measured and evaluated in the energy region 4.98-5.18 MeV. The detection limit of alpha spectrometry measurements has been 0.01 Bq dm -3 . The concentration of plutonium in the 24-hour urine was determined three times in the quarter year intervals. The results are: 54 mBq, 63.2 mBq, 53 mBq, with average 56,7 mBq. From the results of the analyses of plutonium depositions calculated according to ICRP 54 the intake of this radionuclide for the patient was 56.7 kBq. To estimate a committed effective dose (50 years) from the intake of plutonium was used a conversion factor 6.8.10 -5 Sv.Bq -1 (class W). So the expressed committed effective dose received from the plutonium intake is 3.8 Sv. This number is relatively high and all the effective dose will be higher, because the patient was exposed to the other radionuclides too. For example the determination of the rate radionuclides Am-241/Pu-239,Pu-240 was 32-36 % in the fallout after the Chernobyl

Distribution of transuranic nuclides in soils: a review

International Nuclear Information System (INIS)

Essington, E.H.; Fowler, E.B.

1976-01-01

The literature is reviewed to ascertain the degree of movement and the distribution patterns for transuranic and uranium nuclides in soils. Typical plutonium and uranium profiles are presented and an attempt is made to identify unique characteristics causing deviation from an ideal distribution pattern. By far most of the distribution observations are with plutonium and little is reported for uranium and other transuranic nuclides

Plutonium gastrointestinal absorption by adults baboons

International Nuclear Information System (INIS)

Lataillade, G.; Madic, C.; Willemot, J.M.; Germain, P.; Colle, C.; Metivier, H.

1991-01-01

Gastrointestinal absorption of plutonium was investigated in baboons after ingestion of plutonium solution (oxidation states III; IV; V; VI), and plutonium incorporated in soya bean and winkles. We studied the effects of oxidation state and ingested mass for masses ranging from 0.35 μg to 51.6 x 10 +3 μg (4 x 10 -2 to 7776 μg of plutonium per kg of body weight). No clear increase in plutonium retention was shown for concentrations of plutonium smaller than 1 μg/kg. From 1 μg/kg to 1 mg/kg no effects of mass or oxidation state was observed and the mean fractional retention value was 10 -4 . For ingested masses higher than 1 mg/kg the fractional retention values respectively increased for Pu(V) and Pu(III) to (0.9 + 0.2) x 10 -2 and (7.4 + 4.1) x 10 -4 of the ingested mass. This increase might be due to the weak hydrolysis of these oxidation states which would increase gastrointestinal absorption by decrease of hydroxide formation. The fraction of plutonium retained after ingestion of soya bean was (3.0 + 0.5) x 10 -4 about 3 fold higher than the value for 238 Pu nitrate solution. No clear increase in plutonium retention was shown after ingestion of winkles containing 238 Pu. In conclusion, except for high masses of ingested Pu, the retention of which could reach 1% of the ingested dose, our results show that the gastrointestinal transfer factor of 10 -4 proposed by ICRP for gastrointestinal absorption of soluble form of Pu is acceptable, but 10 -3 would provide better safety margin [fr

Disposing of the world's excess plutonium

International Nuclear Information System (INIS)

McCormick, J.M.; Bullen, D.B.

1998-01-01

The authors undertake three key objectives in addressing the issue of plutonium disposition at the end of the Cold War. First, the authors estimate the total global inventory of plutonium both from weapons dismantlement and civil nuclear power reactors. Second, they review past and current policy toward handling this metal by the US, Russia, and other key countries. Third, they evaluate the feasibility of several options (but especially the vitrification and mixed oxide fuel options announced by the Clinton administration) for disposing of the increasing amounts of plutonium available today. To undertake this analysis, the authors consider both the political and scientific problems confronting policymakers in dealing with this global plutonium issue. Interview data with political and technical officials in Washington and at the International Atomic Energy Agency in Vienna, Austria, and empirical inventory data on plutonium from a variety of sources form the basis of their analysis

Selecting a plutonium vitrification process

Energy Technology Data Exchange (ETDEWEB)

Jouan, A. [Centre d`Etudes de la Vallee du Rhone, Bagnols sur Ceze (France)

1996-05-01

Vitrification of plutonium is one means of mitigating its potential danger. This option is technically feasible, even if it is not the solution advocated in France. Two situations are possible, depending on whether or not the glass matrix also contains fission products; concentrations of up to 15% should be achievable for plutonium alone, whereas the upper limit is 3% in the presence of fission products. The French continuous vitrification process appears to be particularly suitable for plutonium vitrification: its capacity is compatible with the required throughout, and the compact dimensions of the process equipment prevent a criticality hazard. Preprocessing of plutonium metal, to convert it to PuO{sub 2} or to a nitric acid solution, may prove advantageous or even necessary depending on whether a dry or wet process is adopted. The process may involve a single step (vitrification of Pu or PuO{sub 2} mixed with glass frit) or may include a prior calcination step - notably if the plutonium is to be incorporated into a fission product glass. It is important to weigh the advantages and drawbacks of all the possible options in terms of feasibility, safety and cost-effectiveness.

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 in depleted uranium penetrators

International Nuclear Information System (INIS)

McLaughlin, J.P.; Leon-Vintro, L.; Smith, K.; Mitchell, P.I.; Zunic, Z.S.

2002-01-01

Depleted Uranium (DU) penetrators used in the recent Balkan conflicts have been found to be contaminated with trace amounts of transuranic materials such as plutonium. This contamination is usually a consequence of DU fabrication being carried out in facilities also using uranium recycled from spent military and civilian nuclear reactor fuel. Specific activities of 239+240 Plutonium generally in the range 1 to 12 Bq/kg have been found to be present in DU penetrators recovered from the attack sites of the 1999 NATO bombardment of Kosovo. A DU penetrator recovered from a May 1999 attack site at Bratoselce in southern Serbia and analysed by University College Dublin was found to contain 43.7 +/- 1.9 Bq/kg of 239+240 Plutonium. This analysis is described. An account is also given of the general population radiation dose implications arising from both the DU itself and from the presence of plutonium in the penetrators. According to current dosimetric models, in all scenarios considered likely ,the dose from the plutonium is estimated to be much smaller than that due to the uranium isotopes present in the penetrators. (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

Assay of low-level plutonium effluents

International Nuclear Information System (INIS)

Hsue, S.T.; Hsue, F.; Bowersox, D.F.

1981-01-01

In the plutonium recovery section at the Los Alamos National Laboratory, an effluent solution is generated that contains low plutonium concentration and relatively high americium concentration. Nondestructive assay of this solution is demonstrated by measuring the passive L x-rays following alpha decay. Preliminary results indicate that an average deviation of 30% between L x-ray and alpha counting can be achieved for plutonium concentrations above 10 mg/L and Am/Pu ratios of up to 3; for plutonium concentrations less than 10 mg/L, the average deviation is 40%. The sensitivity of the L x-ray assay is approx. 1 mg Pu/L

Light water breeder reactor using a uranium-plutonium cycle

International Nuclear Information System (INIS)

Radkowsky, A.; Chen, R.

1990-01-01

This patent describes a light water receptor (LWR) for breeding fissile material using a uranium-plutonium cycle. It comprises: a prebreeder section having plutonium fuel containing a Pu-241 component, the prebreeder section being operable to produce enriched plutonium having an increased Pu-241 component; and a breeder section for receiving the enriched plutonium from the prebreeder section, the breeder section being operable for breeding fissile material from the enriched plutonium fuel. This patent describes a method of operating a light water nuclear reactor (LWR) for breeding fissile material using a uranium-plutonium cycle. It comprises: operating the prebreeder to produce enriched plutonium fuel having an increased Pu-241 component; fueling a breeder section with the enriched plutonium fuel to breed the fissile material

The determination of plutonium isotopes in environmental samples

International Nuclear Information System (INIS)

Siripirom, Lopchai.

1983-01-01

The concentration of plutonium in environmental samples such as soil, water, and surface air in the middle part of Thailand were studied. The surface air were collected only at the fifth floor of the Office of Atomic Energy for Peace (OAEP). Plutonium-242 was used as a tracer. Soil and air samples were dissolved by pyrosulphate fusion, and plutonium was co-precipitated with barium sulfate. Then dissolved the precipitate in perchloric acid. Plutonium was extracted out by using solvent bis-(2-ethylhexyl) phosphoric acid (HDEHP). Plutonium in water samples were coprecipitated with iron (III) hydroxide and were dissolved in 8 M. nitric acid. Then the plutonium was separated out by using anion exchange resin, Dowex 1x4. After the solvent extraction or the anion exchange, plutonium was coprecipitated with cerous hydroxide. The activities of plutonium were measured by a surface barrier detector for about 24 hours. Lower limit of detection for 1,440 minutes is 0.012 pCi. These studies showed that only plutonium-239, 240 was observed. The range of activities of plutonium-239, 240 in soil were 0.002-0.157 pCi/g (dry), in water were 0.1-81 f Ci/l, and in air were 7-330 a Ci/m 3 . However, the plutonium concentrations in these studies are far below the maximum permissible concentration (MPC) recommended by International Commission on Radiological Protection (ICRP) for general population which is equal to 3x10 8 f Ci/l of water and 5x10 6 a Ci/m 3 of air

Plutonium contaminated materials research programme

International Nuclear Information System (INIS)

Higson, S.G.

1986-01-01

The paper is a progress report for 1985 from the Plutonium Contaminated Materials Working Party (PCMWP). The PCMWP co-ordinates research and development on a national basis in the areas of management, treatment and immobilisation of plutonium contaminated materials, for the purpose of waste management. The progress report contains a review of the development work carried out in eight areas, including: reduction of arisings, plutonium measurement, sorting and packaging, washing of shredded combustible PCM, decommissioning and non-combustible PCM treatment, PCM immobilisation, treatment of alpha bearing liquid wastes, and engineering objectives. (UK)

Nuclear legacy. Democracy in a plutonium economy

International Nuclear Information System (INIS)

Barnaby, F.

1997-01-01

There have already been a few hundred known incidents of nuclear smuggling, mostly of small quantities not close to weapons grade material - but one gram of plutonium is more than sufficient to cause significant harm and to pose a substantial threat. The potential for further thefts is growing as the world produces ever more quantities of plutonium, not only from the dismantling of nuclear weapons but also from the separation out of plutonium from spent uranium nuclear reactor fuel elements. Trying to prevent the theft of gram quantities of plutonium would require levels of protection and surveillance unacceptably high in a democratic society. It is unlikely, therefore, that democracy could survive in a plutonium economy

Diffusion in the uranium - plutonium system and self-diffusion of plutonium in epsilon phase

International Nuclear Information System (INIS)

Dupuy, M.

1967-07-01

A survey of uranium-plutonium phase diagram leads to confirm anglo-saxon results about the plutonium solubility in α uranium (15 per cent at 565 C) and the uranium one in ζ 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 12 cm 2 s -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 α autoradiography. Self-diffusion of plutonium in ε phase (bcc) obeys Arrhenius law: D = 2. 10 -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 (βZr, βTi, βHf, U γ ). (author) [fr

Atomic energy policy of Japan, especially plutonium utilization policy

International Nuclear Information System (INIS)

Moriguchi, Y.

1993-01-01

The necessity of plutonium use in Japan is discussed. Basic policy regarding plutonium use and future plutonium utilization programme is described including such an aspect as management of plutonium from dismantled nuclear weapons

Solubility of plutonium dioxide aerosols, in vitro

International Nuclear Information System (INIS)

Newton, G.J.; Kanapilly, G.M.

1976-01-01

Solubility of plutonium aerosols is an important parameter in establishing risk estimates for industrial workers who might accidentally inhale these materials and in evaluating environmental health impacts associated with Pu. In vitro solubility of industrial plutonium aerosols in a simulated lung fluid is compared to similar studies with ultrafine aerosols from laser ignition of delta phase plutonium metal and laboratory-produced spherical particles of 238 PuO 2 and 239 PuO 2 . Although relatively insoluble, industrial plutonium-mixed oxide aerosols were much more soluble than laboratory-produced plutonium dioxide particles. Chain agglomerate aerosols from laser ignition of metallic Pu indicated in vitro dissolution half-times of 10 and 50 days for activity median aerodynamic diameter (AMAD) of 0.7 and 2.3 μm, respectively. Plutonium-containing mixed oxide aerosols indicated dissolution half-times of 40 to 500 days for particles formed by industrial powder comminution and blending. Centerless grinding of fuel pellets yielded plutonium-containing aerosols with dissolution half-times of 1200 to 8000 days. All mixed oxide particles were in the size range 1.0 μm to 2.5 μm AMAD

Ultra-small plutonium oxide nanocrystals: an innovative material in plutonium science.

Science.gov (United States)

Hudry, Damien; Apostolidis, Christos; Walter, Olaf; Janssen, Arne; Manara, Dario; Griveau, Jean-Christophe; Colineau, Eric; Vitova, Tonya; Prüssmann, Tim; Wang, Di; Kübel, Christian; Meyer, Daniel

2014-08-11

Apart from its technological importance, plutonium (Pu) is also one of the most intriguing elements because of its non-conventional physical properties and fascinating chemistry. Those fundamental aspects are particularly interesting when dealing with the challenging study of plutonium-based nanomaterials. Here we show that ultra-small (3.2±0.9 nm) and highly crystalline plutonium oxide (PuO2 ) nanocrystals (NCs) can be synthesized by the thermal decomposition of plutonyl nitrate ([PuO2 (NO3 )2 ]⋅3 H2 O) in a highly coordinating organic medium. This is the first example reporting on the preparation of significant quantities (several tens of milligrams) of PuO2 NCs, in a controllable and reproducible manner. The structure and magnetic properties of PuO2 NCs have been characterized by a wide variety of techniques (powder X-ray diffraction (PXRD), X-ray absorption fine structure (XAFS), X-ray absorption near edge structure (XANES), TEM, IR, Raman, UV/Vis spectroscopies, and superconducting quantum interference device (SQUID) magnetometry). The current PuO2 NCs constitute an innovative material for the study of challenging problems as diverse as the transport behavior of plutonium in the environment or size and shape effects on the physics of transuranium elements. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Total neutron-counting plutonium inventory measurement systems (PIMS) and their potential application to near real time materials accountancy (NRTMA)

International Nuclear Information System (INIS)

Driscall, I.; Fox, G.H.; Orr, C.H.; Whitehouse, K.R.

1988-01-01

A radiometric method of determining the inventory of an operating plutonium plant is described. An array of total neutron counters distributed across the plant is used to estimate hold-up at each plant item. Corrections for the sensitivity of detectors to plutonium in adjacent plant items are achieved through a matrix approach. This paper describes our experience in design, calibration and operation of a Plutonium Inventory Measurement System (PIMS) on an oxalate precipitation plutonium finishing line. Data from a recent trial of Near-Real-Time Materials Accounting (NRTMA) using the PIMS are presented and used to illustrate its present performance and problem areas. The reader is asked to consider what role PIMS might have in future accountancy systems

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

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

Tabulated Neutron Emission Rates for Plutonium Oxide

Energy Technology Data Exchange (ETDEWEB)

Shores, Erik Frederick [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

2017-07-24

This work tabulates neutron emission rates for 80 plutonium oxide samples as reported in the literature. Plutonium-­238 and plutonium-­239 oxides are included and such emission rates are useful for scaling tallies from Monte Carlo simulations and estimating dose rates for health physics applications.

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.

Long time contamination from plutonium

Energy Technology Data Exchange (ETDEWEB)

Fueloep, M; Patzeltova, N; Ragan, P [Inst. of Preventive and Clinical Medicine, Bratislava (Slovakia); Matel, L [Comenius Univ., Bratislava (Slovakia). Department of Nuclear Chemistry

1996-12-31

Plutonium isotopes in the organism of the patient (who had participated in the liquidation works after the Chernobyl accident; for three month he had stayed in the epicenter, where he acted as a chauffeur driving a radioactive material to the place of destination) from urine were determined. For determination of the concentration of Pu-239, Pu-240 in urine a modified radiochemical method was used. After mineralization the sample was separated as an anion-nitrate complex with contact by the anion form of the resin in the column. The resin was washed by 8 M HNO{sub 3}, the 8 M HCl with 0.3 M HNO{sub 3} for removing the other radionuclides. The solution 0.36 M HCl with 0.01 M HF was used for the elution of plutonium. Using the lanthanum fluoride technique the sample was filtrated through a membrane filter. The plutonium was detected in the dry sample. The Pu-239 tracer was used for the evaluation of the plutonium separation efficiency. The alpha spectrometric measurements were carried out with a large area silicon detector. The samples were measured and evaluated in the energy region 4.98-5.18 MeV. The detection limit of alpha spectrometry measurements has been 0.01 Bq dm{sup -3}. The concentration of plutonium in the 24-hour urine was determined three times in the quarter year intervals. The results are: 54 mBq, 63.2 mBq, 53 mBq, with average 56,7 mBq. From the results of the analyses of plutonium depositions calculated according to ICRP 54 the intake of this radionuclide for the patient was 56.7 kBq. To estimate a committed effective dose (50 years) from the intake of plutonium was used a conversion factor 6.8.10{sup -5} Sv.Bq{sup -1} (class W). So the expressed committed effective dose received from the plutonium intake is 3.8 Sv. This number is relatively high and all the effective dose will be higher, because the patient was exposed to the other radionuclides too. (Abstract Truncated)

Plutonium recycle. In-core fuel management

International Nuclear Information System (INIS)

Vincent, F.; Berthet, A.; Le Bars, M.

1985-01-01

Plutonium recycle in France will concern a dozen of PWR 900 MWe controlled in gray mode till 1995. This paper presents the main characteristics of fuel management with plutonium recycle. The organization of management studies will be copied from this developed for classical management studies. Up these studies, a ''feasibility report'' aims at establishing at each stage of the fuel cycle, the impact of the utilization of fuel containing plutonium [fr

Experimental study of contamination by a mixture resulting from the combustion of sodium in the presence of plutonium oxide

International Nuclear Information System (INIS)

Metivier, H.; Masse, R.; Nenot, J.C.; Nolibe, D.; Lafuma, J.

1976-01-01

The introduction into industry of breeder reactors using liquid sodium as the coolant gives rise to fresh radiotoxicological problems; the most likely chemical form in which the plutonium and sodium mixture may be found after a possible accident is a soluble oxide of plutonium(VI) or plutonium(VII). The biological behaviour of such mixtures was analysed in rats and monkeys following parenteral administration. In the case of rats distribution in the organs was analysed from 30 minutes to 30 days following intramuscular contamination. In the monkeys the authors only analysed distribution in the organs after one month. The biological behaviour of the mixture is marked by very high plutonium solubility. The maximum burden in the organs attains roughly 20% of the quantity deposited both in monkeys and rats. The spread of the plutonium proceeds gradually from the day of administration; it indicates that a soluble form of plutonium is present for a long time. Also observed is an increasing osteotropic tendency in the diffusible form. The liver fraction is rapidly removed, if it is assumed that faecal excretion represents biliary excretion. In the experimental conditions selected, the spread of a liquid aerosol of the solution is rapid and constitutes about 10% of the quantity deposited in the airways at the end of inhalation. Treatment with DTPA makes it possible to reduce the body burden, but less efficiently than after contamination by Pu(IV). (author)

The plutonium-oxygen and uranium-plutonium-oxygen systems: A thermochemical assessment

International Nuclear Information System (INIS)

1967-01-01

The report of a panel of experts convened by the IAEA in Vienna in March 1964. It reviews the structural and thermodynamic data for the Pu-O and U-Pu-O systems and presents the conclusions of the panel. The report gives information on preparation, phase diagrams, thermodynamic and vaporization behaviour of plutonium oxides, uranium-plutonium oxides and PuO 2 -MeO x (Me=Be, Mg, Al, Si, W, Th, Eu, Zr, Ce) systems. 167 refs, 27 figs, 17 tabs

Qualitative chemical analysis of plutonium by Alpha spectroscopy

International Nuclear Information System (INIS)

Ramirez G, J Qumica.J.

1994-01-01

In this work the separation and purification of plutonium from irradiated uranium was done. The plutonium, produced by the irradiation of uranium in a nuclear reactor and the β decay of 239 Np, was stabilized to Pu +4 with sodium nitrite. Plutonium was separated from the fission products and uranium by ion exchange using the resin Ag 1 X 8. It was electrodeposited on stainless steel discs and the alpha radioactivity of plutonium was measured in a surface barrier detector. The results showed that plutonium was separated with a radiochemical purity higher than 99 %. (Author)

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.

International shipment of plutonium by air

International Nuclear Information System (INIS)

Mercado, J.E.; McGrogan, J.P.

1995-05-01

In support of the United States (US) Government's decision to place excess plutonium oxide at the US Department of Energy's (DOE) Hanford Site under International Atomic Energy Agency (IAEA) safeguards, the Department of State notified the Congress that a plutonium storage vault at the Plutonium Finishing Plant at the Hanford Site would be added to the eligible facilities list. As part of the preparations to transfer the plutonium oxide under IAEA safeguards, samples of the powder were taken from the inventory to be shipped to the IAEA headquarters in Vienna, Austria, for laboratory analysis. The analysis of these samples was of high priority, and the IAEA requested that the material be shipped by aircraft, the most expeditious method

Pulmonary carcinogenesis from plutonium-containing particles

International Nuclear Information System (INIS)

Thomas, R.G.; Smith, D.M.; Anderson, E.C.

1980-01-01

Induction of lung tumors by various types of radiation is of paramount concern to the nuclear industry. The data presented were obtained by exposing the pulmonary system of Syrian hamsters to particles of zirconium oxide containing various amounts of either plutonium-238 or -239 as the alpha radiation source. These particles were injected intravenously and lodged permanently in the capillary bed of the lung. When less than 20% of the lung tissue was irradiated, simulating the ''hot particle'' mode, tumors were not evident with lung burdens up to 500 nCi plutonium. More diffuse irradiation significantly increased the tumor incidence, with lung burdens of 50 to 150 nCi. When plutonium-laden microspheres were administered intratracheally, tumor production was considerably increased and the addition of 3 mg of iron oxide intratracheally further increased the incidence. Using the zirconium oxide matrix for the carrier of plutonium in aerosol particles produced tumor incidences of up to 50% in Syrian hamsters exposed by inhalation. Initial pulmonary (alveolar) burdens reached 100 nCi of plutonium. Similar inhalation studies using plutonium dioxide alone (no matrix) failed to produce any increase in lung tumorigenesis. The results are discussed in terms of possible mechanisms necessary for lung carcinogenesis. (H.K.)

Verification station for Sandia/Rockwell Plutonium Protection system

International Nuclear Information System (INIS)

Nicholson, N.; Hastings, R.D.; Henry, C.N.; Millegan, D.R.

1979-04-01

A verification station has been designed to confirm the presence of plutonium within a container module. These container modules [about 13 cm (5 in.) in diameter and 23 cm (9 in.) high] hold sealed food-pack cans containing either plutonium oxide or metal and were designed by Sandia Laboratories to provide security and continuous surveillance and safety. After the plutonium is placed in the container module, it is closed with a solder seal. The verification station discussed here is used to confirm the presence of plutonium in the container module before it is placed in a carousel-type storage array inside the plutonium storage vault. This measurement represents the only technique that uses nuclear detectors in the plutonium protection system

Modified titrimetric determination of plutonium using photometric end-point detection

International Nuclear Information System (INIS)

Baughman, W.J.; Dahlby, J.W.

1980-04-01

A method used at LASL for the accurate and precise assay of plutonium metal was modified for the measurement of plutonium in plutonium oxides, nitrate solutions, and in other samples containing large quantities of plutonium in oxidized states higher than +3. In this modified method, the plutonium oxide or other sample is dissolved using the sealed-reflux dissolution method or other appropriate methods. Weighed aliquots, containing approximately 100 mg of plutonium, of the dissolved sample or plutonium nitrate solution are fumed to dryness with an HC1O 4 -H 2 SO 4 mixture. The dried residue is dissolved in dilute H 2 SO 4 , and the plutonium is reduced to plutonium (III) with zinc metal. The excess zinc metal is dissolved with HCl, and the solution is passed through a lead reductor column to ensure complete reduction of the plutonium to plutonium (III). The solution, with added ferroin indicator, is then titrated immediately with standardized ceric solution to a photometric end point. For the analysis of plutonium metal solutions, plutonium oxides, and nitrate solutions, the relative standard deviation are 0.06, 0.08, and 0.14%, respectively. Of the elements most likely to be found with the plutonium, only iron, neptunium, and uranium interfere. Small amounts of uranium and iron, which titrate quantitatively in the method, are determined by separate analytical methods, and suitable corrections are applied to the plutonium value. 4 tables, 4 figures

The economics of plutonium recycle

International Nuclear Information System (INIS)

James, R.A.

1977-11-01

The individual cost components and the total fuel cycle costs for natural uranium and uranium-plutonium mixed oxide fuel cycles for CANDU-PHW reactors are discussed. A calculation is performed to establish the economic conditions under which plutonium recycle would be economically attractive. (auth)

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

Plutonium uniqueness

International Nuclear Information System (INIS)

Silver, G.L.

1984-01-01

A standard is suggested against which the putative uniqueness of plutonium may be tested. It is common folklore that plutonium is unique among the chemical elements because its four common oxidation states can coexist in the same solution. Whether this putative uniqueness appears only during transit to equilibrium, or only at equilibrium, or all of the time, is not generally made clear. But while the folklore may contain some truth, it cannot be put to test until some measure of 'uniqueness' is agreed upon so that quantitative comparisons are possible. One way of measuring uniqueness is as the magnitude of the product of the mole fractions of the element at equilibrium. A 'coexistence index' is defined and discussed. (author)

Determination of plutonium in soils by mass spectrometry

International Nuclear Information System (INIS)

Storms, H.A.; Carlson, D.C.; Hunter, F.F.

1974-01-01

A procedure is described in which mass spectrometry is utilized for the determination of plutonium in soils. Using this procedure we have measured plutonium isotopic compositions at concentrations as low as 2 x 10 -14 grams Pu per gram soil. A thermal ionization source with canoe-shaped rhenium filament, is utilized in the mass spectrometer. The plutonium, when loaded onto the filament, is contained in a single Dowex-1 resin bead which is about 350 micrometers in diameter. Concentrating the plutonium within this single bead is a key step in the procedure and produces a relatively clean plutonium fraction. The resin bead also serves as an effective diffusion barrier such that the plutonium is prevented from being removed with the lower boiling impurities. The Pu remains in the bead until the temperature is sufficiently high for efficient production of Pu + ions. Plutonium ionization efficiencies as high as 2.5 percent have been measured

Surplus plutonium disposition draft environmental impact statement. Volume 2

International Nuclear Information System (INIS)

1998-07-01

On May 22, 1997, DOE published a Notice of Intent (NOI) in the Federal Register (62 Federal Register 28009) announcing its decision to prepare an environmental impact statement (EIS) that would tier from the analysis and decisions reached in connection with the Storage and Disposition of Weapons-Usable Fissile Materials Final Programmatic EIS (Storage and Disposition PEIS). DOE's disposition strategy allows for both the immobilization of surplus plutonium and its use as mixed oxide (MOX) fuel in existing domestic, commercial reactors. The disposition of surplus plutonium would also involve disposal of the immobilized plutonium and MOX fuel (as spent nuclear fuel) in a geologic repository. The Surplus Plutonium Disposition Environmental Impact Statement analyzes alternatives that would use the immobilization approach (for some of the surplus plutonium) and the MOX fuel approach (for some of the surplus plutonium); alternatives that would immobilize all of the surplus plutonium; and the No Action Alternative. The alternatives include three disposition facilities that would be designed so that they could collectively accomplish disposition of up to 50 metric tons (55 tons) of surplus plutonium over their operating lives: (1) the pit disassembly and conversion facility would disassemble pits (a weapons component) and convert the recovered plutonium, as well as plutonium metal from other sources, into plutonium dioxide suitable for disposition; (2) the immobilization facility would include a collocated capability for converting nonpit plutonium materials into plutonium dioxide suitable for immobilization and would be located at either Hanford or SRS. DOE has identified SRS as the preferred site for an immobilization facility; (3) the MOX fuel fabrication facility would fabricate plutonium dioxide into MOX fuel. Volume 2 contains the appendices to the report and describe the following: Federal Register notices; contractor nondisclosure statement; adjunct melter

Addressing mixed waste in plutonium processing

International Nuclear Information System (INIS)

Christensen, D.C.; Sohn, C.L.; Reid, R.A.

1991-01-01

The overall goal is the minimization of all waste generated in actinide processing facilities. Current emphasis is directed toward reducing and managing mixed waste in plutonium processing facilities. More specifically, the focus is on prioritizing plutonium processing technologies for development that will address major problems in mixed waste management. A five step methodological approach to identify, analyze, solve, and initiate corrective action for mixed waste problems in plutonium processing facilities has been developed

Microdistribution and Long-Term Retention of 239Pu (NO3)4 in the Respiratory Tracts of an Acutely Exposed Plutonium Worker and Experimental Beagle Dogs

Energy Technology Data Exchange (ETDEWEB)

Nielsen, Christopher E.; Wilson, Dulaney A.; Brooks, Antone L.; McCord, Stacey; Dagle, Gerald E.; James, Anthony C.; Tolmachev, Sergei Y.; Thrall, Brian D.; Morgan, William F.

2012-11-01

The long-term retention of inhaled soluble forms of plutonium raises concerns as to the potential health effects in persons working in nuclear energy or the nuclear weapons program. The distributions of long-term retained inhaled plutonium-nitrate [239Pu (NO3)4] deposited in the lungs of an accidentally exposed nuclear worker (Human Case 0269) and in the lungs of experimentally exposed beagle dogs with varying initial lung depositions were determined via autoradiographs of selected histological lung, lymph node, trachea, and nasal turbinate tissue sections. These studies showed that both the human and dogs had a non-uniform distribution of plutonium throughout the lung tissue. Fibrotic scar tissue effectively encapsulated a portion of the plutonium and prevented its clearance from the body or translocation to other tissues and diminished dose to organ parenchyma. Alpha radiation activity from deposited plutonium in Human Case 0269 was observed primarily along the sub-pleural regions while no alpha activity was seen in the tracheobronchial lymph nodes of this individual. However, relatively high activity levels in the tracheobronchial lymph nodes of the beagles indicated the lymphatic system was effective in clearing deposited plutonium from the lung tissues. In both the human case and beagle dogs, the appearance of retained plutonium within the respiratory tract was inconsistent with current biokinetic models of clearance for soluble forms of plutonium. Bound plutonium can have a marked effect on the dose to the lungs and subsequent radiation exposure has the potential increase in cancer risk.

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

Spectrographic analysis of plutonium (1960); L'analyse spectrographique du plutonium (1960)

Energy Technology Data Exchange (ETDEWEB)

Artaud, J; Chaput, M; Robichet, J [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

1960-07-01

Various possibilities for the spectrographic determination of impurities in plutonium are considered. The application of the 'copper spark' method, of sparking on graphite and of fractional distillation in the arc are described and discussed in some detail (apparatus, accessories, results obtained). (author) [French] On examine diverses possibilites pour le dosage spectrographique des impuretes dans le plutonium. On decrit et discute plus particulierement de l'application des methodes 'copper spark', de l'etincelage sur graphite et de la distillation fractionnee dans l'arc (montages, accessoires, resultats obtenus). (auteur)

Monitoring of wastes containing plutonium. Necessity and method

International Nuclear Information System (INIS)

Sousselier, Y.; Pottier, P.

1979-01-01

Importance of problems set by wastes containing plutonium is rapidly growing. Plutonium is not a waste, recycling limits heavily the quantity of plutonium to be stored with wastes. Optimized waste management must take definitive storage and economical limits of plutonium recovery into account. Waste monitoring is a must for safety, economy and waste management. Methods used require reliability, simplicity, sensibility and accuracy particularly for threshold detection [fr

Studies on removal of plutonium from oxalic acid containing hydrochloric acid solutions

Energy Technology Data Exchange (ETDEWEB)

Ghadse, D R; Noronha, D M; Joshi, A R [Fuel Chemistry Division, Bhabha Atomic Research Centre, Mumbai (India)

1994-06-01

Solution containing hydrochloric acid, oxalic acid and considerable quantities of plutonium may be generated while recycling of scrap produced during the metallic fuel fabrication. Plutonium from such waste is normally recovered by anion exchange method after the destruction of oxalic acid using suitable oxidising agent. Solvent extraction and ion exchange methods are being explored in this laboratory for recovery of Pu from oxalic acid containing HCl solutions without prior destruction of oxalic acid. This paper describes the results on the determination of distribution ratios for extraction of Pu(IV) from hydrochloric acid using Aliquot-336 or HDEHP under varying experimental conditions. (author). 5 refs., 5 tabs.

A neutron well counter for plutonium assay in 200 l waste drums

International Nuclear Information System (INIS)

Eyrich, W.; Kuechle, M.; Shafiee, M.

1979-05-01

A neutron well counter is briefly described which will be used for monitoring the plutonium content of 200 l barrels in the waste treatment plant of the Kernforschungszentrum Karlsruhe. Measurements on simulated waste were made to study the influence of matrix material and non-homogeneous plutonium distribution. The variation in detection efficiency could be reduced from 28% to 10% when the signals from inner and outer neutron detectors in the polyethylene annulus are counted separately and a correction is applied, using this information. This method is superior to the source addition technique. Coincidence counting shows a larger variation which could not be reduced to below 18%. (orig.) [de

Selected radionuclides. Tritium, carbon-14, krypton-85, strontium-90, iodine, caesium 137, radon, plutonium

International Nuclear Information System (INIS)

1983-01-01

The release of radioactive materials to the environment potentially exposes populations to ionizing radiation and increases the risk of incurring deleterious health effects. The associations of released amounts to effects establish the health criteria for radionuclides. This report provides background information in establishing such health criteria for 14 C, 85 Kr, 90 Sr, 137 Cs, Radon, Plutonium, Iodine and Tritium, including environmental behaviour, sources, transport to man and dosimetry. A brief summary of the general aspects of radiation effects and of radiation protection considerations is presented

Extraction and purification of plutonium by a tertiary amine; Extraction et purification du plutonium par une amine tertiaire

Energy Technology Data Exchange (ETDEWEB)

Trentinian, M de; Chesne, A [Commissariat a l' Energie Atomique, Fontenay aux Roses, Section de Chimie des Actimides (France).Centre d' Etudes Nucleaires; Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

1960-07-01

Trilaurylamine diluted with a paraffinic solvent (dodecane) was studied as part of the research dealing with the separation and purification of plutonium. The physical properties (solubility of nitrates in the amine as a function of temperature) and the resistance to radiations of this substance were examined. The extraction characteristics of nitric solutions of plutonium, uranium and certain fission products are given as a function of the following factors: concentration of the various ions in solution, valency states. A method of plutonium purification based on these results is presented. (author) [French] La trilaurylamine diluee par un solvant paraffinique (dodecane) a ete etudiee dans le cadre des recherches concernant la separation et la purification du plutonium. Une etude des caracteres physiques (solubilite des nitrates dans l'amine en fonction de la temperature) s'ajoute a celle de la tenue aux radiations de ce corps. Les caracteristiques d'extraction de solutions nitriques de plutonium, uranium, et certains produits de fission, sont donnes en fonction des facteurs suivants: concentration des differents ions en solution, etats de valence. On presente une methode de purification du plutonium basee sur ces resultats. (auteur)

Transuranium element toxicity: dose-response relationships at low exposure levels. Summary and speculative interpretation relative to exposure limits

International Nuclear Information System (INIS)

Thompson, R.C.

1975-01-01

A summary is given of information on transuranium element toxicity and the correlation of this information with current established exposure limits. It is difficult to calculate a biologically relevant radiation dose from deposited plutonium; it is exposure that must be controlled in order to prevent biological effect, and if the relationship between exposure and effect is known, then radiation dose is of no concern. There are extensive data on the effects of plutonium in bone. Results of studies at the University of Utah indicate that plutonium in beagles may be as much as ten times more toxic than radium. It has been suggested that this toxicity ratio may be even higher in man than in the beagle dog because of differences in surface-to-volume ratios and differences in the rate of burial of surface-deposited plutonium. The present capabilities for extrapolating dose-effect relationships seem to be limited to the setting of upper limits, based on assumptions of linearity and considerations related to natural background

Evaluation of plutonium at Enewetak Atoll

International Nuclear Information System (INIS)

Wilson, D.W.; Ng, Y.C.; Robison, W.L.

1975-01-01

An extensive survey was carried out in 1972 to 1973 to assess the current radiological status of Enewetok Atoll. The radionuclides detected in the Atoll environment were studied for their potential contributions to the dose commitment of the returning population according to several pathways of exposure. Plutonium was detected in air and in the terrestrial and aquatic environment at concentrations that varied from background levels due to world-wide fallout to levels several orders-of-magnitude above. The dose commitments from plutonium via the terrestrial food chain and inhalation vary according to the postulated living pattern. The dosages via marine foods can be expected to be insensitive to living pattern and to exceed those via terrestrial foods. Plutonium would contribute nearly all of the dosage via inhalation, but this pathway ranks low in overall importance compared with the food-chain and external-dose pathways. Although the potential dose from plutonium via all pathways is low relative to that from 60 Co, 90 Sr and 137 Cs, plutonium will still remain in the Atoll environment after the other makor isotopes have decayed away. (author)

Long-term plutonium storage: Design concepts

International Nuclear Information System (INIS)

Wilkey, D.D.; Wood, W.T.; Guenther, C.D.

1994-01-01

An important part of the Department of Energy (DOE) Weapons Complex Reconfiguration (WCR) Program is the development of facilities for long-term storage of plutonium. The WCR design goals are to provide storage for metals, oxides, pits, and fuel-grade plutonium, including material being held as part of the Strategic Reserve and excess material. Major activities associated with plutonium storage are sorting the plutonium inventory, material handling and storage support, shipping and receiving, and surveillance of material in storage for both safety evaluations and safeguards and security. A variety of methods for plutonium storage have been used, both within the DOE weapons complex and by external organizations. This paper discusses the advantages and disadvantages of proposed storage concepts based upon functional criteria. The concepts discussed include floor wells, vertical and horizontal sleeves, warehouse storage on vertical racks, and modular storage units. Issues/factors considered in determining a preferred design include operational efficiency, maintenance and repair, environmental impact, radiation and criticality safety, safeguards and security, heat removal, waste minimization, international inspection requirements, and construction and operational costs

Technical considerations and policy requirements for plutonium management

International Nuclear Information System (INIS)

Christensen, D.C.; Dinehart, S.M.; Yarbro, S.L.

1995-01-01

The goals for plutonium management have changed dramatically over the past few years. Today, the challenge is focused on isolating plutonium from the environment and preparing it for permanent disposition. In parallel, the requirements for managing plutonium are rapidly changing. For example, there is a significant increase in public awareness on how facilities operate, increased attention to environmental safety and health (ES and H) concerns, greater interest in minimizing waste, more emphasis on protecting material from theft, providing materials for international inspection, and a resurgence of interest in using plutonium as an energy source. Of highest concern, in the immediate future, is protecting plutonium from theft or diversion, while the national policy on disposition is debated. These expanded requirements are causing a broadening of responsibilities within the Department of Energy (DOE) to include at least seven organizations. An unavoidable consequence is the divergence in approach and short-term goals for managing similar materials within each organization. The technology base does exist, properly, safely, and cost effectively to extract plutonium from excess weapons, residues, waste, and contaminated equipment and facilities, and to properly stabilize it. Extracting the plutonium enables it to be easily inventoried, packaged, and managed to minimize the risk of theft and diversion. Discarding excess plutonium does not sufficiently reduce the risk of diversion, and as a result, long-term containment of plutonium from the environment may not be able to be proven to the satisfaction of the public

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

Technical considerations and policy requirements for plutonium management

International Nuclear Information System (INIS)

Christensen, D.C.; Dinehart, S.M.; Yarbro, S.L.

1996-01-01

The goals for plutonium management have changed dramatically over the past few years. Today, the challenge is focused on isolating plutonium from the environment and preparing it for permanent disposition. In parallel, the requirements for managing plutonium are rapidly changing. For example, there is a significant increase in public awareness on how facilities operate, increased attention to environmental safety and health (ES and H) concerns, greater interest in minimizing waste, more emphasis on protecting material from theft, providing materials for international inspection, and a resurgence of interest in using plutonium as an energy source. Of highest concern, in the immediate future, is protecting plutonium from theft or diversion, while the national policy on disposition is debated. These expanded requirements are causing a broadening of responsibilities within the Department of Energy (DOE) to include at least seven organizations. An unavoidable consequence is the divergence in approach and short-term goals for managing similar materials within each organization. The technology base does exist, properly, safely, and cost effectively to extract plutonium from excess weapons, residues, waste, and contaminated equipment and facilities, and to properly stabilize it. Extracting the plutonium enables it to be easily inventoried, packaged, and managed to minimize the risk of theft and diversion. Discarding excess plutonium does not sufficient reduce the risk of diversion, and as a result, long-term containment of plutonium from the environment may not be able to be proven to the satisfaction of the public

Plutonium again (smuggling and movements)

International Nuclear Information System (INIS)

Anon.

1994-01-01

A link is discounted between nuclear proliferation and the recently discovered smuggled plutonium from the former Soviet Union at Munich airport and other places in Germany. It is argued that governments wishing to obtain nuclear materials to develop a weapons programme would not arrange to have it smuggled in a suitcase. Instead, it is speculated that a link exists between the plutonium smuggling incidents and the desire to promote the production of mixed oxide (MOX) fuel. Such incidents, by further raising public anxiety, may be intended to turn public opinion in favour of MOX fuel production as a sensible way of getting rid of surplus plutonium. (UK)

Safe handling of plutonium: a panel report

Energy Technology Data Exchange (ETDEWEB)

1974-01-01

This guide results from a meeting of a Panel of Experts held by the International Atomic Energy Agency on 8 to 12 November 1971. It is directed to workers in research laboratories handling plutonium in gram amounts. Contents: aspects of the physical and chemical properties of plutonium; metabolic features of plutonium; facility design features for safe handling of plutonium (layout of facility, working zones, decontamination room, etc.); glove boxes; health surveillance (surveillance of environment and supervision of workers); emergencies; organization. Annexes: types of glove boxes; tables; mobile ..cap alpha.. air sampler; aerosol monitor; bio-assay limits of detection; examples of contamination control monitors.

Plutonium disposition via immobilization in ceramic or glass

Energy Technology Data Exchange (ETDEWEB)

Gray, L.W.; Kan, T.; Shaw, H.F.; Armantrout, A.

1997-03-05

The management of surplus weapons plutonium is an important and urgent task with profound environmental, national, and international security implications. In the aftermath of the Cold War, Presidential Policy Directive 13, and various analyses by renown scientific, technical, and international policy organizations have brought about a focused effort within the Department of Energy to identify and implement paths for the long term disposition of surplus weapons- usable plutonium. The central goal of this effort is to render surplus weapons plutonium as inaccessible and unattractive for reuse in nuclear weapons as the much larger and growing stock of plutonium contained in spent fuel from civilian reactors. One disposition option being considered for surplus plutonium is immobilization, in which the plutonium would be incorporated into a glass or ceramic material that would ultimately be entombed permanently in a geologic repository for high-level waste.

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 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

Testing plutonium fuel assembly production for fast-neutron reactors

International Nuclear Information System (INIS)

Nougues, B.; Benhamou, A.; Bertothy, G.; Lepetit, H.

1975-01-01

The main characteristics of plutonium fuel elements for fast breeder reactors justify specific test procedures and special techniques. The specific tests relating to the Pu content consist of Pu enrichment and distribution tests, determination of the O/M ratio and external contamination tests. The specific tests performed on fuel configuration are: testing of sintered pellet diameter, testing of pin welding and checking of internal assmbly [fr

The extraction of plutonium with triethylene glycol dichloride

International Nuclear Information System (INIS)

Aikin, A.M.; Moss, M.; Bruce, T.

1951-03-01

The extraction of plutonium by triethylene glycol dichloride (trigly) has been investigated briefly. The effect of (1) the valence state of the plutonium, (2) the concentration of nitric acid, (3) the concentration of ammonium nitrate and (4) the conditioning of the trigly was measured. The solubility of plutonium IV in trigly was found to be 70 mgms/ml. Solutions of plutonium in trigly and in concentrated nitric acid solutions have been examined spectrophotometrically. (author)

The extraction of plutonium with triethylene glycol dichloride

Energy Technology Data Exchange (ETDEWEB)

Aikin, A M; Moss, M; Bruce, T

1951-03-15

The extraction of plutonium by triethylene glycol dichloride (trigly) has been investigated briefly. The effect of (1) the valence state of the plutonium, (2) the concentration of nitric acid, (3) the concentration of ammonium nitrate and (4) the conditioning of the trigly was measured. The solubility of plutonium IV in trigly was found to be 70 mgms/ml. Solutions of plutonium in trigly and in concentrated nitric acid solutions have been examined spectrophotometrically. (author)

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)

Standard practice for preparation and dissolution of plutonium materials for analysis

CERN Document Server

American Society for Testing and Materials. Philadelphia

2008-01-01

1.1 This practice is a compilation of dissolution techniques for plutonium materials that are applicable to the test methods used for characterizing these materials. Dissolution treatments for the major plutonium materials assayed for plutonium or analyzed for other components are listed. Aliquants of the dissolved samples are dispensed on a weight basis when one of the analyses must be highly reliable, such as plutonium assay; otherwise they are dispensed on a volume basis. 1.2 The treatments, in order of presentation, are as follows: Procedure Title Section Dissolution of Plutonium Metal with Hydrochloric Acid 9.1 Dissolution of Plutonium Metal with Sulfuric Acid 9.2 Dissolution of Plutonium Oxide and Uranium-Plutonium Mixed Oxide by the Sealed-Reflux Technique 9.3 Dissolution of Plutonium Oxide and Uranium-Plutonium Mixed Oxides by Sodium Bisulfate Fusion 9.4 Dissolution of Uranium-Plutonium Mixed Oxides and Low-Fired Plutonium Oxide in Beakers 9.5 1.3 The values stated in SI units are to be re...

Civil plutonium held in France in December 31, 2000

International Nuclear Information System (INIS)

2002-02-01

Spent fuels comprise about 1% of plutonium which is separated during the reprocessing and recycled to prepare the mixed uranium-plutonium fuel (MOX), which in turn is burnt in PWRs. Plutonium can be in a non-irradiated or separated form, or in an irradiated form when contained in the spent fuel. Each year, in accordance with the 1997 directives relative to the management of plutonium, France has to make a status of its civil plutonium stock and communicate it to the IAEA using a standard model form. This short document summarizes the French plutonium stocks at the end of 1999 and 2000. (J.S.)

Plutonium determination by isotope dilution

International Nuclear Information System (INIS)

Lucas, M.

1980-01-01

The principle is to add to a known amount of the analysed solution a known amount of a spike solution consisting of plutonium 242. The isotopic composition of the resulting mixture is then determined by surface ionization mass spectrometry, and the plutonium concentration in the solution is deduced, from this measurement. For irradiated fuels neutronic studies or for fissile materials balance measurements, requiring the knowledge of the ratio U/Pu or of concentration both uranium and plutonium, it is better to use the double spike isotope dilution method, with a spike solution of known 233 U- 242 Pu ratio. Using this method, the ratio of uranium to plutonium concentration in the irradiated fuel solution can be determined without any accurate measurement of the mixed amounts of sample and spike solutions. For fissile material balance measurements, the uranium concentration is determined by using single isotope dilution, and the plutonium concentration is deduced from the ratio Pu/U and U concentration. The main advantages of isotope dilution are its selectivity, accuracy and very high sensitivity. The recent improvements made to surface ionization mass spectrometers have considerably increased the precision of the measurements; a relative precision of about 0.2% to 0.3% is obtained currently, but it could be reduced to 0.1%, in the future, with a careful control of the experimental procedures. The detection limite is around 0.1 ppb [fr

Plutonium and americium separation from salts

International Nuclear Information System (INIS)

Hagan, P.G.; Miner, F.J.

1976-01-01

Salts or materials containing plutonium and americium are dissolved in hydrochloric acid, heated, and contacted with an alkali metal carbonate solution to precipitate plutonium and americium carbonates which are thereafter readily separable from the solution

Behavior of plutonium interacting with bentonite and sulfate-reducing anaerobic bacteria

International Nuclear Information System (INIS)

Kudo, A.; Zheng, J.; Cayer, I.; Fujikawa, Y.; Yoshikawa, H.; Ito, M.

1997-01-01

The interactions between sulfate reducing anaerobic bacteria and plutonium, with or without bentonite present, were investigated using distribution coefficients [Kd (ml/g)] as an index of the radionuclide behavior. Plutonium Kds for living bacteria varied within a large range, from 1,804 to 112,952, depending on the pH, while the Kds ranged from 1,180 to 5,931 for dead bacteria. In general, living bacteria had higher plutonium Kds than dead bacteria. Furthermore, the higher Kd values of 39,677 to 106,915 for living bacteria were obtained for a pH range between 6.83 and 8.25, while no visible pH effect was observed for dead bacteria. These Kd values were obtained using tracers for both 236 Pu and 239 Pu, which can check the experimental procedures and mass balance. Another comparison was conducted for plutonium Kd values of mixtures of living bacteria with bentonite and sterilized bacteria with bentonite. The range of Kd values for the non-sterilized bacteria with bentonite were 1,194 to 83,648 while Kd values for the sterilized bacteria with bentonite were from 624 to 17,236. Again, the Kd values for the living bacteria with bentonite were higher than those of sterilized bacteria with bentonite. In other words, the presence of living anaerobic bacteria with bentonite increased, by roughly 50 times, the Kd values of 239 Pu when compared to the mixture of dead bacteria with bentonite. The results indicate that the effects of anaerobic bacteria within the engineered barrier system (in this case bentonite) will play a significant role in the behavior of plutonium in geologic repositories

Work at Aldermaston on plutonium binding with biological systems

International Nuclear Information System (INIS)

Popplewell, D.S.

1976-01-01

Over a number of years, the Chemistry Division of AWRE, Aldermaston, studied the nature of plutonium in various biological systems. The object of the work was to identify those natural products of the body which play a part in the transport and deposition of accidental intakes of plutonium. These results should be of value in formulating more effective therapeutic measures for plutonium removal from the body. The paper reviews the work at AWRE on the interaction of plutonium with serum and rat liver. Experiments on the uptake of plutonium into cell cultures are described. The aim of these experiments was to see whether a model system could be set up for testing the efficacy by which chelating agents could remove plutonium from within cells. A simple hypothesis is presented for the mode of transport of plutonium within animals. (author)

Further Evaluation of the Neutron Resonance Transmission Analysis (NRTA) Technique for Assaying Plutonium in Spent Fuel

Energy Technology Data Exchange (ETDEWEB)

J. W. Sterbentz; D. L. Chichester

2011-09-01

This is an end-of-year report (Fiscal Year (FY) 2011) for the second year of effort on a project funded by the National Nuclear Security Administration's Office of Nuclear Safeguards (NA-241). The goal of this project is to investigate the feasibility of using Neutron Resonance Transmission Analysis (NRTA) to assay plutonium in commercial light-water-reactor spent fuel. This project is part of a larger research effort within the Next-Generation Safeguards Initiative (NGSI) to evaluate methods for assaying plutonium in spent fuel, the Plutonium Assay Challenge. The second-year goals for this project included: (1) assessing the neutron source strength needed for the NRTA technique, (2) estimating count times, (3) assessing the effect of temperature on the transmitted signal, (4) estimating plutonium content in a spent fuel assembly, (5) providing a preliminary assessment of the neutron detectors, and (6) documenting this work in an end of the year report (this report). Research teams at Los Alamos National Laboratory (LANL), Lawrence Berkeley National Laboratory (LBNL), Pacific Northwest National Laboratory (PNNL), and at several universities are also working to investigate plutonium assay methods for spent-fuel safeguards. While the NRTA technique is well proven in the scientific literature for assaying individual spent fuel pins, it is a newcomer to the current NGSI efforts studying Pu assay method techniques having just started in March 2010; several analytical techniques have been under investigation within this program for two to three years or more. This report summarizes work performed over a nine month period from January-September 2011 and is to be considered a follow-on or add-on report to our previous published summary report from December 2010 (INL/EXT-10-20620).

HENC performance evaluation and plutonium calibration

International Nuclear Information System (INIS)

Menlove, H.O.; Baca, J.; Pecos, J.M.; Davidson, D.R.; McElroy, R.D.; Brochu, D.B.

1997-10-01

The authors have designed a high-efficiency neutron counter (HENC) to increase the plutonium content in 200-L waste drums. The counter uses totals neutron counting, coincidence counting, and multiplicity counting to determine the plutonium mass. The HENC was developed as part of a Cooperative Research and Development Agreement between the Department of Energy and Canberra Industries. This report presents the results of the detector modifications, the performance tests, the add-a-source calibration, and the plutonium calibration at Los Alamos National Laboratory (TA-35) in 1996

Plutonium determination by spectrophotometry of plutonium (VI): control of the nuclear fuel reprocessing plant

Energy Technology Data Exchange (ETDEWEB)

Grison, J [Compagnie Generale des Matieres Nucleaires (COGEMA), Centre de la Hague, 50 - Cherbourg (France)

1980-10-01

The plutonium (VI) spectrophotometric determination, after AgO oxidation in 3 M nitric acid medium, is used for the running-control of the nuclear fuel reprocessing plant at La Hague. Analytical device used in glove-box or shielded-cell is briefly described. This method is fast, sensitive, unfailing and gives simple effluents. It is applied by day and night shifts, during Light Water Reactor fuel reprocessing campaign, for 0.5 mg/l up to 20 g/l plutonium solutions. Reference solution measurements have a 0.8 to 1.4 % relative standard deviation; duplicate plutonium determinations give a 0.3% relative standard deviation for sample analysis. There is a discrepancy (- 0.3% to - 0.9%) between the spectrophotometric method results and the isotopic dilution analysis.

Plutonium determination by spectrophotometry of plutonium (VI): control of the nuclear fuel reprocessing plant

International Nuclear Information System (INIS)

Grison, J.

1980-01-01

The plutonium (VI) spectrophotometric determination, after AgO oxidation in 3 M nitric acid medium, is used for the running-control of the nuclear fuel reprocessing plant at La Hague. Analytical device used in glove-box or shielded-cell is briefly described. This method is fast, sensitive, unfailing and gives simple effluents. It is applied by day and night shifts, during Light Water Reactor fuel reprocessing campaign, for 0.5 mg/l up to 20 g/l plutonium solutions. Reference solution measurements have a 0.8 to 1.4 % relative standard deviation; duplicate plutonium determinations give a 0.3% relative standard deviation for sample analysis. There is a discrepancy (- 0.3% to - 0.9%) between the spectrophotometric method results and the isotopic dilution analysis [fr

Fifty years of plutonium exposure to the Manhattan Project plutonium workers: an update.

Science.gov (United States)

Voelz, G L; Lawrence, J N; Johnson, E R

1997-10-01

Twenty-six white male workers who did the original plutonium research and development work at Los Alamos have been examined periodically over the past 50 y to identify possible health effects from internal plutonium depositions. Their effective doses range from 0.1 to 7.2 Sv with a median value of 1.25 Sv. As of the end of 1994, 7 individuals have died compared with an expected 16 deaths based on mortality rates of U.S. white males in the general population. The standardized mortality ratio (SMR) is 0.43. When compared with 876 unexposed Los Alamos workers of the same period, the plutonium worker's mortality rate was also not elevated (SMR = 0.77). The 19 living persons have diseases and physical changes characteristic of a male population with a median age of 72 y (range = 69 to 86 y). Eight of the twenty-six workers have been diagnosed as having one or more cancers, which is within the expected range. The underlying cause of death in three of the seven deceased persons was from cancer, namely cancer of prostate, lung, and bone. Mortality from all cancers was not statistically elevated. The effective doses from plutonium to these individuals are compared with current radiation protection guidelines.

Plutonium recycle in PWR reactors (Brazilian Nuclear Program)

International Nuclear Information System (INIS)

Rubini, L.A.

1978-02-01

An evaluation is made of the material requirements of the nuclear fuel cycle with plutonium recycle. It starts from the calculation of a reference reactor and allows the evaluation of demand under two alternatives of nuclear fuel cycle for Pressurized Water Reactors (PWR): without plutonium recycle; and with plutonium recycle. Calculations of the reference reactor have been carried out with the CELL-CORE codes. For plutonium recycle, the concept of uranium and plutonium homogeneous mixture has been adopted, using self-produced plutonium at equilibrium, in order to get minimum neutronic perturbations in the reactor core. The refueling model studied in the reference reactor was the 'out-in' scheme with a constant number of changed fuel elements (approximately 1/3 of the core). Variations in the material requirements were studied considering changes in the installed nuclear capacity of PWR reactors, the capacity factor of these reactors, and the introduction of fast breeders. Recycling plutonium produced inside the system can reach economies of about 5%U 3 O 8 and 6% separative work units if recycle is assumed only after the 5th operation cycle of the thermal reactors. The cumulative amount of fissile plutonium obtained by the Brazilian Nuclear Program of PWR reactors by 1991 should be sufficient for a fast breeder with the same capacity as Angra 2. For the proposed fast breeder programs, the fissile plutonium produced by thermal reactors is sufficient to supply fast breeder initial necessities. Howewer, U 3 O 8 and SWU economy with recycle is not significant when the proposed fast breeder program is considered. (Author) [pt

Work surface for soluble plutonium

International Nuclear Information System (INIS)

Silver, G.L.

2005-01-01

A three-dimensional work surface for aqueous plutonium is illustrated. It is constructed by means of estimating work as a function of the ambient pH and redox potential in a plutonium solution. The surface is useful for illustrating the chemistry of disproportionation reactions. Work expressions are easier to use than work integrals. (author)

Oxidation-state maxima in plutonium chemistry

International Nuclear Information System (INIS)

Silver, G.L.

2013-01-01

Maxima in the fractions of the trivalent and hexavalent oxidation states of plutonium are inherent in the algebra of its disproportionation reactions. The maxima do not support overall disproportionation equations as satisfactory representations of aqueous plutonium. (author)

A technique for the assessment of the masses of residual plutonium in gloveboxes using thermoluminescent dosimeters

International Nuclear Information System (INIS)

Day, B.; Godward, D.F.

1979-01-01

A means of measuring the mass of residual plutonium in gloveboxes in the size range 1 to 10 m 3 has been developed using multiple thermoluminescent detectors. By optimising the location and the number of detectors, and by using suitable filtration, the mean response from them has been made insensitive to the distribution and the composition of the plutonium. It is possible to detect 10 g of plutonium in the largest glovebox considered. The measurement and mass estimation processes have been reduced to simple operations which can be carried out by skilled industrial staff. The routine application of the technique has been arranged to minimise disturbance to be production work going on in the gloveboxes by making unattended measurements during silent hours

Plutonium recycling and the problem of nuclear proliferation

International Nuclear Information System (INIS)

Albright, D.; Feiveson, H.S.

1988-01-01

A typical 1-gigawatt light water reactor (LWR), the dominant commercial power reactor type today, operating at 70% capacity factor, generates approximately 250 kilograms of plutonium annually. This plutonium, which is produced in the reactor through neutron capture by uranium-238, is then discharged from the reactor along with the other constituents of the spent fuel. About 70% of the plutonium, or 175 kilograms, consists of fissile (odd-numbered) plutonium isotopes. As long as the plutonium discharged from the reactor is left intermixed with the highly radioactive fission products also contained in the spent fuel, it cannot readily be used for power or for weapons. However, upon chemical separation from the radioactive fission products and other components of the spent reactor fuel, the plutonium produced each year in a gigawatt reactor could be used, either in recycled fuel (to replace about 175 kilograms of U-235 in a power reactor) or to provide the fissile material for more than 25 nuclear warheads. Commercial separation of plutonium and the introduction of nuclear fuel cycles using recycled plutonium, which are now impending in several countries, force one to balance the probable increased risks of nuclear proliferation due to these activities against various economic and other motives that have been forwarded in their defense. The authors undertake an assessment of this balancing in this article

Solid-phase extraction of plutonium in various oxidation states from simulated groundwater using N-benzoylphenylhydroxylamine

International Nuclear Information System (INIS)

Perevalov, S.A.; Malofeeva, G.I.; Kuzovkina, E.V.; Spivakov, B.Ya.

2013-01-01

Solid-phase extraction of plutonium in different individual and mixed oxidation states from simulated groundwater (pH 8.5) was studied. The extraction of plutonium species was carried out in a dynamic mode using DIAPAK C16 cartridges modified by N-benzoylphenylhydroxylamine (BPHA). It was shown that the extent of recovery depends on the oxidation state of plutonium. The extraction of Pu(IV) was at the level of 98-99% regardless of the volume and flow-rate of the sample solution. Pu(V) was extracted by 90-95% and 75-80% from 10- and 100-mL aliquots of the samples, respectively, whereas the extraction of Pu(VI) did not exceed 45-50%. An equimolar mixture of Pu(IV), Pu(V), and Pu(VI) was extracted by 74%. The distribution coefficients (K d ) and kinetic exchange capacities (S) of plutonium in various oxidation states were measured. It was found that during the sorption process, Pu(V) was reduced to Pu(IV) by 80-90% after an hour-long contact with the solid phase. Pu(VI) is reduced to Pu(V) by 34% and to Pu(IV) by 55%. In the case of mixed-valent solution of plutonium, only Pu(V) and Pu(IV) were found in the effluents. (author)

The use of plutonium rapides surregenerateurs aspects techniques et economiques

International Nuclear Information System (INIS)

Guillet, H.; Delayre, R.; Mougniot, J.C.; Ferrari, A.

1977-01-01

Nuclear energy production utilizing U 235 and U 238 inevitably results in the formation of plutonium. Some of this is directly used by the reactor in power production. Some reactors, e.g. the Candu type, burn most of their plutonium ''in situ''. However the surplus quantity of plutonium produced is increasing, and by 1990 the world stock of plutonium is predicted to be about 1000 tons (300 tons in Europe and 400 in the USA). This represents approximately 0.1 Q of potential power, where Q=10 21 joules. Proposals for dealing with this plutonium include its storage, either as irradiated fuel or as a refined substance (plutonium nitrate or oxide); its use in thermal reactors as a substitute for U 235 ; its use in fast breeder reactors which can act as consumers of plutonium as well as producers and which can therefore regulate the world's plutonium stocks. Leaving aside the question of storage, certain technical conditions must be fulfilled. It is essential that reprocessing plants should be operational and available in adequate numbers. An industry able to make use of plutonium should be developed with large capacity units. There seem to be no problems with plutonium use in reactors: conclusive experiments have proved the accuracy of calculations regarding plutonium recycling in thermal reactors and a number of fast breeders have proved the possibility of using plutonium in them. Experience acquired during the past ten years permits us to deal with the safety and safeguards problem of using plutonium. Many economic questions remain, however, including questions affecting the utilization of plutonium, such as the cost of regenerating irradiated fuel and of making fuel, and questions affecting the strategy of using plutonium in different ways, such as the price at which it should be sold. Also the cost of producing electricity using plutonium is not yet clear. It is unavoidable that plutonium will be used in nuclear power development. The technical and economic problems

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

A literature study of the behaviour of cesium, strontium and plutonium in the soil-plant ecosystem

International Nuclear Information System (INIS)

Nielsen, B.; Strandberg, M.

1988-07-01

Literature on the occurrence of radiocesium (primarily 137CS) in the soil-plant system with emphasis on the influence of treatment on its root uptake, was reviewed. The aim was to study root uptake of radiocesium in order to estimate the applicability of suitable counter measures in cases of contamination of arable land with plutonium, radiostrontium and, in particular, radiocesium. To what extent 136CS is available to, and absorbed by, the plant and how it is distributed and absorbed in the soil is described. The physiological uptake of plutonium from soil through roots to plant parts lying above ground constitutes minor health hazards to population from the ingestion of vegetables. Extensive use of root fruits, might indicate that there is a risk present in areas of high plutonium soil concentration, because plutonium is adsorbed to root molecules, especially if soil and peel are not discarded. Another risk lies in the resuspension of plutonium deposited on the soil surface. As mentioned above, the impact of the leakage of plutonium from the Chernobyl accident was negligible in distant areas. The effects in the vicinity of the reactor, might have been important. In small areas with high levels of plutonium contamination removal of the top soil layer will be effective. Because of the high toxity and long half-life of plutonium, the risk involved merely in isolating such an area will be to high, because the plutonium may be further dispersed. In larger areas, deep ploughing to a depth of 30-40 cm or more, if feasible, is a possibility. Local factors have to be considered, e.g. position of bedrock, groundwater, soil parameters etc. Deep ploughing combined with previous dispersion of clay minerals, lime or humus or a combination, might be a solution, and should be followed by limiting crops to those with roots concentrated in the surface layer and with smallest attainable concentration ratios for plutonium. Cereals might fill this demand. 188 refs. (AB)

Recommendations for plutonium colloid size determination

International Nuclear Information System (INIS)

Kosiewicz, S.T.

1984-02-01

This report presents recommendations for plutonium colloid size determination and summarizes a literature review, discussions with other researchers, and comments from equipment manufacturers. Four techniques suitable for plutonium colloid size characterization are filtration and ultrafiltration, gel permeation chromatography, diffusion methods, and high-pressure liquid chromatography (conditionally). Our findings include the following: (1) Filtration and ultrafiltration should be the first methods used for plutonium colloid size determination because they can provide the most rapid results with the least complicated experimental arrangement. (2) After expertise has been obtained with filtering, gel permeation chromatography should be incorporated into the colloid size determination program. (3) Diffusion methods can be used next. (4) High-pressure liquid chromatography will be suitable after appropriate columns are available. A plutonium colloid size characterization program with filtration/ultrafiltration and gel permeation chromatography has been initiated

The availability of plutonium and americium in Irish Sea sediments for re-dissolution

International Nuclear Information System (INIS)

McDonald, P.; Vives i Batlle, J.; Bousher, A.; Whittall, A.; Chambers, N.

2001-01-01

The availability of plutonium and americium, for re-dissolution from offshore sediments into Irish Sea water, has been examined. Sediments collected from the mud-patch near the Cumbrian coast were characterized in terms of spatial location, particle size, partitioning of radionuclides with respect to physico-chemical bonds and availability of actinides for release into seawater. Sequential extraction investigations revealed that plutonium was predominantly associated with strongly bound sesquioxide and organic complex fractions. Americium was associated mainly with the organic complex fraction, but a significant fraction was in carbonate form. Sediment/water re-dissolution experiments with and without stirring were compared to simulate the effect of disturbing bed sediment. After 1 week, neither set of re-dissolution data provided significant trends between dissolved activity and time. Stirred systems appeared to release 2.5 times more plutonium and americium into seawater than unstirred systems. Measured 239,240Pu and 241Am distribution coefficients (K d values) were both typically approximately 10 5 l kg -1 . 241Am K d values are an order of magnitude lower than previously reported for the north-eastern Irish Sea, but similar to western Irish Sea values. Overall, the fractions of plutonium and americium available for re-dissolution from bed sediment are very low at <0.1%, with proportionally more plutonium being released than americium. These findings lend further support for the extrapolation of laboratory-derived information to environmental conditions

Accumulation and transport of soil plutonium in liquid waste discharge areas at Los Alamos

International Nuclear Information System (INIS)

Hakonson, T.E.; Nyhan, J.W.; Purtymun, W.D.

1976-01-01

Plutonium inventory estimates for the surface 12.5 cm of soil in Mortandad Canyon did not reflect all the plutonium added to the canyon during a 7 month interval. The methods used in this study indicated that about 2 mCi 238 Pu and 0 mCisup(239,240)Pu were added to the canyon during the interval, compared with known additions of 5.5 mCi 238 Pu and 0.4 mCisup(239,240)Pu. The discrepancy likely was the result of the large sampling variability, indicating that inventory changes in this order (i.e. up to 17%) are not detectable with any certainty. However, factors other than sampling variability may be involved, including losses of plutonium to depths exceeding 12.5 cm. The relative distribution of plutonium within the canyon demonstrates that transport has occurred beyond the extent of surface water and that runoff from summer rainstorms can serve as a radionuclide transport vector in landscapes exhibiting these hydrologic features. There was a highly significant relationship between suspended sediment concentrations and total amounts of radioactivity in water. The flow rates achieved during the runoff event play an important part in determining the total amount of sediment and thus radioactivity transported downstream. The storm runoff event sampled during this study resulted in the downstream transport of about 1-2% of the sediment inventories of plutonium. (author)

Plutonium-contaminated fragments at the Taranaki site at Maralinga

International Nuclear Information System (INIS)

Burns, P.A.; Cooper, M.B.; Duggleby, J.C.; Mika, J.F.; Williams, G.A.

1986-07-01

A detailed assessment is presented of the distribution of plutonium-contaminated fragments and sub-millimetre particles in the vicinity of the Taranaki site at the former U.K. Atomic Weapons Test Range at Maralinga in South Australia. The area which is contaminated with fragments has been divided into three general regions with the designations 'heavily contaminated', 'moderately contaminated' and 'plumes'. The average surface density, activity and estimated total number of fragments are presented for each region. Average surface densities of all fragments with americium-241 activities greater than 2 kBq are estimated to be 33, 7 and 2 m -2 for the 'heavily contaminated', 'moderately contaminated' and 'plumes' regions respectively. The total number of such fragments is estimated to be in excess of three million which accounts for a total plutonium activity of approximately 0.8 TBq. The implications of these results for a rehabilitation program are discussed

Analytic determination of plutonium in the environment

International Nuclear Information System (INIS)

Ballada, J.

1967-01-01

The work described in this report was undertaken with a view to determining the plutonium content in the fall-out from nuclear explosions. In the first part are described in turn the importance of the problems due to the plutonium, the physico-chemical properties of the radioelement and the biological dangers which it presents. A detailed and critical analysis is made of the radio-toxicological determination of the plutonium as reported in the literature prior to this report. The second part consists in the presentation of a judicious choice of techniques making it possible to determine plutonium in air, rain-water, soils and ash. After a detailed description of the measurement equipment and the operational techniques which have been developed, a justification of these techniques is given with particular reference to their sensitivity and specificity. After a brief conclusion concerning the preceding chapters, the results are presented. These are then discussed in the ease of each element in which the plutonium has been determined. This discussion is concluded by a consideration of the importance of the occurrence of fall-out plutonium on problems relating to public health. From a consideration of 200 analyses carried out, it is concluded that the contribution of plutonium to the exposure of populations is still very small compared to that of natural radiation and that due to such fission products as strontium 90. The report includes 63 literature references, 26 figures and 11 tables. (author) [fr

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.)

Plutonium peroxide precipitation: review and current research

International Nuclear Information System (INIS)

Hagan, P.G.; Miner, F.J.

1980-01-01

Increasing the HNO 3 concentration decreases the filtration time but increases the plutonium concentration in the filtrate. A compromise was therefore necessary. If a minimum plutonium concentration is required in the filtrate, the acidity could be lowered to 1.9M with an approximate doubling in the filtration time. The H 2 O 2 concentration has little effect on filtration time. However, the higher the H 2 O 2 concentration, the less plutonium lost to the filtrate. Concentrations higher than the 22 moles/mole Pu recommended (at least up to 30 molar which was the highest investigated) would be beneficial if reagent costs are not excessive and production capacity exists for destroying the excess H 2 O 2 in the filtrate. Although the effect is not large, filtration time is shorter and the plutonium concentration in the filtrate is lower if metallic impurities are present. The slowest rate of H 2 O 2 addition investigated gives a plutonium peroxide precipitate with the fastest filtration time. The rate of addition has very little effect on the plutonium concentration in the filtrate. The temperature has little effect on the filtration time. 14 0 C is recommended since decomposition of H 2 O 2 would be slower at 14 0 C than at 22 0 C (min. Pu content in the filtrate). The effect of digestion time on both the filtration time and the plutonium content in the filtrate is minor, so the shortest digestion time investigated is recommended

Fluorescent determination of neptunium in plutonium

International Nuclear Information System (INIS)

Alexandruk, V.M.; Babaev, A.S.; Dem'yanova, T.A.; Stepanov, A.V.

1991-01-01

This paper describes a new procedure for direct determination of Neptunium in Plutonium using laser induced time resolved fluorescence method. The procedure based on measurement of fluorescence intensity of Neptunium followed its concentration in effective layer of pellet of calcium fluoride. Detection limit of determination of Neptunium is 2 10 -12 g. At the level of Neptunium content in Plutonium more than 5 ppm relative standard deviation is equal 0.08-0.12. For carrying out of single measurement it is necessary neither more nor less 5 mkg Plutonium

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.'

New developments in the air transport of plutonium

International Nuclear Information System (INIS)

Andersen, J.A.

1978-01-01

A new package for the air transport of plutonium has been developed in response to a United States Public Law which restricts the US air transport of plutonium except for small medical devices. This new package, called PAT-1 for plutonium air transportable package model 1, is the result of the NRC-sponsored PARC (plutonium accident resistant container) project at Sandia Laboratories, Albuquerque. The PAT-1 package is designed to meet or exceed new criteria specified in NUREG-0360. These include a severe test sequence of impact (greater than 250 KTS) on an unyielding target, crush, puncture, slash, a large JP-4 fire for 1 hour, followed by water immersion, with stringent acceptance standards on plutonium release, nuclear shielding, and nuclear criticality. The PAT-1 package design features a high energy absorption capability with high-level fire protection. It weighs approximately 227 kg (500 lb) when loaded with 2 kg PuO 2 , and can accommodate up to 25 watts thermal energy from the plutonium load

The calculation of annual limits of intake for plutonium-239 in man using a bone model which allows for plutonium burial and recycling