Estimation and characterization of decontamination and decommissioning solid waste expected from the Plutonium Finishing Plant

International Nuclear Information System (INIS)

Millar, J.S.; Pottmeyer, J.A.; Stratton, T.J.

1995-01-01

Purpose of the study was to estimate the amounts of equipment and other materials that are candidates for removal and subsequent processing in a solid waste facility when the Hanford Plutonium Finishing Plant is decontaminated and decommissioned. (Building structure and soil are not covered.) Results indicate that ∼5,500 m 3 of solid waste is expected to result from the decontamination and decommissioning of the Pu Finishing Plant. The breakdown of the volumes and percentages of waste by category is 1% dangerous solid waste, 71% low-level waste, 21% transuranic waste, 7% transuranic mixed waste

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.

An overview of plutonium-238 decontamination and decommissioning (D and D) projects at Mound

International Nuclear Information System (INIS)

Bond, W.H.; Davis, W.P.; Draper, D.G.; Geichman, J.R.; Harris, J.C.; Jaeger, R.R.; Sohn, R.L.

1987-01-01

Mound is currently decontaminating for restricted reuse and/or decommissioning for conditional release four major plutonium-238 contaminated facilities that contained 1700 linear feet of gloveboxes and associated equipment and services. Several thousand linear feet of external underground piping, associated tanks, and contaminated soil are being removed. Two of the facilities contain ongoing operations and will be reused for both radioactive and nonradioactive programs. Two others will be completely demolished and the land area will become available for future DOE building sites. An overview of the successful techniques and equipment used in the decontamination and decommissioning of individual pieces of equipment, gloveboxes, services, laboratories, sections of buildings, entire buildings, and external underground piping, tanks, and soil in a highly populated residential area is described and pictorially presented

Preliminary trials of the decontamination of plutonium contaminated material with arklone

International Nuclear Information System (INIS)

Gaudie, S.C.; Wilkins, J.D.

1984-07-01

The use of Arklone (1,1,2-trichloro-1,2,2-trifluoroethane) as a decontamination reagent in conjunction with an ultrasonic bath for plutonium contaminated non-combustible wastes has been investigated. For stainless and mild steel contaminated with PuO 2 , the surface contamination can be reduced to 5 to 10 μg Pu/cm 2 , while for painted steel the final level is 1 to 2 μg Pu/cm 2 . Aqueous reagents (e.g. H 2 O 1M NaOH) tend to give better results with the stainless steel, particularly if a surface active reagent is used, giving a residual level of 1 to 2 μg Pu/cm 2 . A wide range of additives have been tried in conjunction with the Arklone to improve its effectiveness (e.g. anionic, cationic and neutral surface active reagents) with little success. A commercial mixture, Arklone W, which is an Arklone/water/surfactant emulsion gave the best results. With the exception of Arklone W, very poor results were obtained with Arklone (and various additives) with plutonium nitrate contamination. (author)

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

International Nuclear Information System (INIS)

CHARBONEAU, S.L.

2006-01-01

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

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

Integrated five station nondestructive assay system for the support of decontamination and decommissioning of a former plutonium mixed oxide fuel fabrication facility

International Nuclear Information System (INIS)

Caldwell, J.T.; Bieri, J.M.; Hastings, R.D.; Horton, W.S.; Kuckertz, T.H.; Kunz, W.E.; Plettenberg, K.; Smith, L.D.

1990-01-01

The goal of a safe, efficient and economic decontamination and decommissioning of plutonium facilities can be greatly enhanced through the intelligent use of an integrated system of nondestructive assay equipment. We have designed and fabricated such a system utilizing five separate NDA stations integrated through a single data acquisition and management personal computer-based controller. The initial station utilizes a passive neutron measurement to determine item Pu inventory to the 0.1 gm level prior to insertion into the decontamination cell. A large active neutron station integrated into the cell is used to measure decontamination effectiveness at the 10 nci/gm level. Cell Pu buildup at critical points is monitored with passive neutron detectors. An active neutron station having better than 1 mg Pu assay sensitivity is used to quantify final compacted waste pucks outside the cell. Bulk Pu in various forms and isotopic enrichments is quantified in a combined passive neutron coincidence and high resolution gamma ray spectrometer station outside the cell. Item control and Pu inventory are managed with bar code labeling and a station integrating algorithm. Overall economy is achieved by multiple station use of the same expensive hardware such as the neutron generator

PNL size reduction and decontamination facilities and capabilities

International Nuclear Information System (INIS)

Allen, R.P.; Fetrow, L.K.; McCoy, M.W.

1983-07-01

Studies sponsored by the US Department of Energy at Pacific Northwest Laboratory (PNL) have resulted in the development of an effective, integrated size reduction and decontamination system for transuranically contaminated components. Using this system, a reduction of more than 95% in the volume of transuranic waste requiring interim storage and eventual geologic disposal has been achieved for typical plutonium contaminated glove boxes. This paper describes the separate preparation, size reduction, decontamination and waste treatment operations and facilities that have been developed and demonstrated as part of this work

Treatment of simulated plutonium-containing wastewater by ultrafiltration-reverse osmosis technology

International Nuclear Information System (INIS)

Xiong Zhonghua; Fan Xianhua; Luo Deli; Wang Tuo; Chen Qi

2008-01-01

Ultrafiltration and reverse osmosis were employed for the treatment of low level radioactive water containing plutonium. The system consists of ultrafiltration module with hollow fibre membrane and reverse osmosis module with spiral membrane. The decontamination efficiency and volume concentration ratio affected by technical parameters were explored in the experiment. The results show that the decontamination efficiency achieves 99.94% and the volume concentration ratio achieves 12.5 at pH=10 for solution fed into the membrane separation system. This technology will be applied in radioactive waste minimization as a new treatment method. (authors)

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

LASL experience in decontamination of the environment

International Nuclear Information System (INIS)

Ahlquist, A.J.

1981-01-01

This discussion represents one part of a major effort in soil decontamination at the Los Alamos site. A contaminated industrial waste line in the Los Alamos townsite was removed, and a plutonium incineration facility, and a filter building contaminated with actinium-227 were dismantled. The former plutonium handling facility has been decontaminated, and canyons and an old firing site contaminated with strontium-90 have been surveyed

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

International Nuclear Information System (INIS)

McCutcheon, E.B.

1975-05-01

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

SAFETY STUDIES TO MEASURE EXOTHERMIC REACTIONS OF SPENT PLUTONIUM DECONTAMINATION CHEMICALS USING WET AND DRY DECONTAMINATION METHODS

International Nuclear Information System (INIS)

HOPKINS, A.M.; JACKSON, G.W.; MINETTE, M.; EWALT, J.; COOPER, T.; SCOTT, P.; JONES, S.; SCHEELEY, R.

2005-01-01

The Plutonium Finishing Plant (PFP) at the Hanford site in Eastern Washington is currently being decommissioned by Fluor Hanford. Chemicals being considered for dccontamination of gloveboxes in PFP include cerium (IV) nitrate in a nitric acid solution, and proprietary commercial solutions that include acids and sequestering agents. Aggressive chemicals are commonly used to remove transuranic contaminants from process equipment to allow disposal of the equipment as low level waste. Fluor's decontamination procedure involves application of chemical solutions as a spray on the contaminated surfaces, followed by a wipe-down with rags. Alternatively, a process of applying oxidizing Ce IV ions contained in a gel matrix and vacuuming a dry gel material is being evaluated. These processes effectively transfer the transuranic materials to rags or a gel matrix which is then packaged as TRU waste and disposed

Precipitation process for supernate decontamination

International Nuclear Information System (INIS)

Lee, L.M.; Kilpatrick, L.L.

1982-11-01

A precipitation and adsorption process has been developed to remove cesium, strontium, and plutonium from water-soluble, high-level radioactive waste. An existing waste tank serves as the reaction vessel and the process begins with the addition of a solution of sodium tetraphenylborate and a slurry of sodium titanate to the contained waste salt solution. Sodium tetraphenylborate precipitates the cesium and sodium titanate adsorbs the strontium and plutonium. The precipitate/adsorbate is then separated from the decontaminated salt solution by crossflow filtration. This new process offers significant capital savings over an earlier ion exchange process for salt decontamination. Chemical and small-scale engineering studies with actual waste are reported. The effect of many variables on the decontamination factors and filter performance are defined

Electrolytic decontamination of stainless steel using a basic electrolyte

International Nuclear Information System (INIS)

Childs, E.L.; Long, J.L.

1981-01-01

An electrolytic plutonium decontamination process or stainless steel was developed for use as the final step in a proposed radioactive waste handling and decontamination facility to be construced at the Rockwell International Rocky Flats plutonium handling facility. This paper discusses test plan, which was executed to compare the basic electrolyte with phosphoric acid and nitric acid electrolytes. 1 ref

Evaluation of arklone for the decontamination of non-combustible plutonium contaminated materials

International Nuclear Information System (INIS)

Gaudie, S.C.; Wilkins, J.D.; Turner, A.D.

1986-04-01

The use of Arklone (1,1,2 trichloro-, 1,2,2 trifluoroethane) as a decontamination reagent for plutonium contaminated non-combustible wastes has been investigated on a laboratory scale. Arklone has been found to be effective for the removal of loose Pu0 2 contamination - in particular from organic surfaces - from both synthetic and genuine waste. Of the range of contacting techniques investigated, ultrasonics was the best, though vibrocleaning and low pressure spraying performed well. For painted mild steel, paint stripping followed by treatment with Marshall's solution (an aqueous solution of oxalic acid and hydrogen peroxide) cleaned the surface to below 10 -4 μCi/cm 2 . Alternatively , electrochemical techniques could be used - particularly electrodissolution in nitric acid for stainless steel - to reduce contamination levels to 10 -5 μCi/cm 2 . (author)

Electrochemical decontamination of Pu contaminated stainless steel

International Nuclear Information System (INIS)

Turner, A.D.; Pottinger, J.S.; Junkison, A.R.

1983-08-01

Electrochemical decontamination has been demonstrated to be very effective in removing plutonium nitrate contamination (0.5 μg cm -2 ) on stainless steels. The amount of metal dissolved to achieve a DF of 10 2 to 10 3 was 2 to 7 μm depending on the electrolyte used. In unstirred electrolytes 1M HNO 3 , 1M HNO 3 /0.1M NaF, 5M HNO 3 perform best. Under stirred electrolyte conditions, there is a general marginal fall in effectiveness except for 5M HNO 3 where there is a slight improvement. The optimum performance is a compromise between maximizing the electrolyte throwing power and minimizing substrate surface roughening during decontamination. (author)

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

International Nuclear Information System (INIS)

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

2007-01-01

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

Disposition of TA-33-21, a plutonium contaminated experimental facility

International Nuclear Information System (INIS)

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

1975-01-01

The report discusses the decontamination, demolition and disposal of a plutonium contaminated experimental physics facility which housed physics experiments with plutonium from 1951 until 1960. The results of preliminary decontamination efforts in 1960 are reported along with health physics, waste management, and environmental aspects of final disposition work accomplished during 1974 and 1975. (auth)

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.

ASSESSING CHEMICAL HAZARDS AT THE PLUTONIUM FINISHING PLANT FOR PLANNING FUTURE DECONTAMINATION AND DECOMMISSIONING

International Nuclear Information System (INIS)

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

2007-01-01

This paper documents the fiscal year (FY) 2006 assessment to evaluate potential chemical and radiological hazards associated with vessels and piping in the former plutonium process areas at Hanford's Plutonium Finishing Plant (PFP). Evaluations by PFP engineers as design authorities for specific systems and other subject-matter experts were conducted to identify the chemical hazards associated with transitioning the process areas for the long-term layup of PFP before its eventual final decontamination and decommissioning (D and D). D and D activities in the main process facilities were suspended in September 2005 for a period of between 5 and 10 years. A previous assessment conducted in FY 2003 found that certain activities to mitigate chemical hazards could be deferred safely until the D and D of PFP, which had been scheduled to result in a slab-on-grade condition by 2009. As a result of necessary planning changes, however, D and D activities at PFP will be delayed until after the 2009 time frame. Given the extended project and plant life, it was determined that a review of the plant chemical hazards should be conducted. This review to determine the extended life impact of chemicals is called the ''Plutonium Finishing Plant Chemical Hazards Assessment, FY 2006''. This FY 2006 assessment addresses potential chemical and radiological hazard areas identified by facility personnel and subject-matter experts who reevaluated all the chemical systems (items) from the FY 2003 assessment. This paper provides the results of the FY 2006 chemical hazards assessment and describes the methodology used to assign a hazard ranking to the items reviewed

DECONTAMINATION/DESTRUCTION TECHNOLOGY DEMONSTRATION FOR ORGANICS IN TRANSURANIC WASTE

Energy Technology Data Exchange (ETDEWEB)

Chris Jones; Javier Del Campo; Patrick Nevins; Stuart Legg

2002-08-01

The United States Department of Energy's Savannah River Site has approximately 5000 55-gallon drums of {sup 238}Pu contaminated waste in interim storage. These may not be shipped to WIPP in TRUPACT-II containers due to the high rate of hydrogen production resulting from the radiolysis of the organic content of the drums. In order to circumvent this problem, the {sup 238}Pu needs to be separated from the organics--either by mineralization of the latter or by decontamination by a chemical separation. We have conducted ''cold'' optimization trials and surrogate tests in which a combination of a mediated electrochemical oxidation process (SILVER II{trademark}) and ultrasonic mixing have been used to decontaminate the surrogate waste materials. The surrogate wastes were impregnated with copper oxalate for plutonium dioxide. Our process combines both mineralization of reactive components (such cellulose, rubber, and oil) and surface decontamination of less reactive materials such as polyethylene, polystyrene and polyvinylchloride. By using this combination of SILVER II and ultrasonic mixing, we have achieved 100% current efficiency for the destruction of the reactive components. We have demonstrated that: The degree of decontamination achieved would be adequate to meet both WIPP waste acceptance criteria and TRUPACT II packaging and shipping requirements; The system can maintain near absolute containment of the surrogate radionuclides; Only minimal pre-treatment (coarse shredding) and minimal waste sorting are required; The system requires minimal off gas control processes and monitoring instrumentation; The laboratory trials have developed information that can be used for scale-up purposes; The process does not produce dioxins and furans; Disposal routes for secondary process arisings have already been demonstrated in other programs. Based on the results from Phase 1, the recommendation is to proceed to Phase 2 and use the equipment at Savannah

A solvent proceed for the extraction of the irradiate uranium and plutonium in the reactor core; Un procede par solvant pour l'extraction du plutonium de l'uranium irradie dans les piles

Energy Technology Data Exchange (ETDEWEB)

Goldschmidt, B; Regnaut, P; Prevot, I [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1955-07-01

Description of the conditions of plutonium, fission products and of uranium separation by selective extraction of the nitrates by organic solvent, containing a simultaneous extraction of plutonium and uranium, followed by a plutonium re-extraction after reduction, and an uranium re-extraction. The rates of decontamination being insufficient in this first stage, we also describes the processes of decontamination permitting separately to get the rates wanted for uranium and plutonium. Finally, we describes the beginning of the operation that consists in a nitric dissolution of the active uranium while capturing the products of gaseous fission, as well as the final concentration of the products of fission in a concentrated solution. (authors) [French] Description des conditions de separation du plutonium, des produits de fission et de l'uranium au moyen d'une extraction selective des nitrates par solvant organique, comprenant une extraction simultanee du plutonium et de l'uranium, suivie d'une reextraction du plutonium apres reduction, et d'une reextraction de l'uranium. Les taux de decontamination etant insuffisants dans ce premier stade, on decrit egalement les processus de decontamination permettant separement d'obtenir les taux desires pour l'uranium et le plutonium. Enfin, on decrit aussi le debut de l'operation qui consiste en une dissolution nitrique de l'uranium actif en captant les produits de fission gazeux, ainsi que la concentration finale des produits de fission sous forme de solution concentree. (auteurs)

Determination of plutonium in environmental samples by controlled valence in anion exchange

International Nuclear Information System (INIS)

Chen Qingjiang, Yu Yixuan; Nies, H.; Aarkorg, A.; Nielsen, S.P.; Dahlgaard, H.; Mandrup, K.

1993-01-01

The title method was successfully used for collecting 239,240 Pu from 200 litres of seawater by coprecipitation with 16 g FeSO 4 *7H 2 O under reducing conditions without filtering. The plutonium is leached by concentrated HNO 3 +HCl from the coprecipitate and solid particles. The precipitate is heated at 400 deg C and digested in aqua regia. Na 2 SO 3 and NaNO 2 have been applied to obtain Pu 4+ valence state in 0.5-1N HNO 3 for different samples. Plutonium and thorium are coadsorbed on anionic resin from 8N HNO 3 . The column is eluted with 8N HNO 3 containing fresh NaO 2 to keep the Pu 4 '+ state for uranium decontamination. The system of the column is changed from 8N HNO 3 to concentrated HCl with 50 ml concentrated HCl containing a few milligrams of NaNO 2 . Further decontamination of thorium was achieved by elution with concentrated HCl instead of 9N HCl. The plutonium is successfully stripped by H 2 O, NaOH, 2N HNO 3 and 0.5 N HNO 3 containing 0.01M NaNO 3 . The chemical yield of plutonium for a 200 l seawater sample is 60-80%. The resolution of the electroplated thin source is very good. (author) 2 refs.; 1 fig.; 6 tabs

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.

The ultrasonic copper and brass decontamination study; Etude de la decontamination du cuivre et des laitons en presence d'ultra-sons

Energy Technology Data Exchange (ETDEWEB)

Courtault, J; Kerdelleau, J de; Mestre, E [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1965-07-01

The use of ultra-sounds as a decontamination technic does not bring an absolute solution. As a function of the materials it seemed necessary to find what was the optimum conditions for using the ultra-sounds and to define not only the ultra-sonic factors but also the chemical solutions which bring some appreciable decontamination factors without bringing any too important corrosion processus. This report gives the results of this study applied to copper and brass. This study allowed to select some effective treatment baths on the two types of contamination: plutonium and fission products. (authors) [French] L'emploi des ultra-sons comme technique de decontamination n'amene pas une solution absolue. Il est apparu necessaire de rechercher en fonction de la nature du materiau a decontaminer quelles etaient les conditions optimales d'utilisation des ultra-sons et de definir alors non seulement les facteurs ultrasoniques mais encore les solutions chimiques qui apportent des facteurs de decontamination appreciables sans amener des phenomenes de corrosion trop importants. Ce rapport donne les resultats de cette etude appliquee au cuivre et aux laitons. Cette etude a permis de selectionner des bains de traitement efficaces dans les deux cas de contamination: plutonium et produits de fission. (auteurs)

Health physics manual of good practices for plutonium facilities. [Contains glossary

Energy Technology Data Exchange (ETDEWEB)

Brackenbush, L.W.; Heid, K.R.; Herrington, W.N.; Kenoyer, J.L.; Munson, L.F.; Munson, L.H.; Selby, J.M.; Soldat, K.L.; Stoetzel, G.A.; Traub, R.J.

1988-05-01

This manual consists of six sections: Properties of Plutonium, Siting of Plutonium Facilities, Facility Design, Radiation Protection, Emergency Preparedness, and Decontamination and Decommissioning. While not the final authority, the manual is an assemblage of information, rules of thumb, regulations, and good practices to assist those who are intimately involved in plutonium operations. An in-depth understanding of the nuclear, physical, chemical, and biological properties of plutonium is important in establishing a viable radiation protection and control program at a plutonium facility. These properties of plutonium provide the basis and perspective necessary for appreciating the quality of control needed in handling and processing the material. Guidance in selecting the location of a new plutonium facility may not be directly useful to most readers. However, it provides a perspective for the development and implementation of the environmental surveillance program and the in-plant controls required to ensure that the facility is and remains a good neighbor. The criteria, guidance, and good practices for the design of a plutonium facility are also applicable to the operation and modification of existing facilities. The design activity provides many opportunities for implementation of features to promote more effective protection and control. The application of ''as low as reasonably achievable'' (ALARA) principles and optimization analyses are generally most cost-effective during the design phase. 335 refs., 8 figs., 20 tabs.

Chemical decontamination of metals

International Nuclear Information System (INIS)

Partridge, J.A.; Lerch, R.E.

1979-10-01

A metal decontamination process based upon removal of contamination by treatment with a cerium (IV)-nitric acid solution (or other redox agent in nitric acid) is feasible and highly promising. The technique is effective in dissolving the surface layer of stainless steel. Dissolution rates of approximately 1.5 mils/h were demonstrated with cerium (IV)-nitric acid solutions. Removal of plutonium contamination from stainless steel was demonstrated in laboratory tests, in which activity levels were reduced from greater than 5 x 10 5 counts per minute to nondetectable levels in approximately one hour at 90 0 C. Removal of paint from stainless steel surfaces was also demonstrated. Advantages of this process over other chemical solutions include: (1) The solutions are not high salt systems; therefore, there is potentially less waste generated. (2) Cerium(IV) in nitric acid is a good dissolution agent for plutonium oxide. (3) Regeneration of Ce(IV) during the decontamination is accomplished by electrolysis. (4) The process should be effective for irregularly shaped equipment. (5) It could be effective as a spray or a flow-through system. 13 figures

A portable concentrator for processing plutonium

International Nuclear Information System (INIS)

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

1995-01-01

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

Investigation of electro-kinetic methods for soil decontamination

International Nuclear Information System (INIS)

Shabanova, A.N.

2000-01-01

The choices of effective methods for ecological system decontamination, their perfection and introduction into practical use have been actual tasks for the Ural region. The objective of this work has been to study the potentials of electrical kinetics method of ISOTRON Corporation (US) for decontamination of the Urals soils. Results obtained have shown the method proposed to be usable for decontaminating some types of soils from strontium and plutonium; it is low effective for decontamination in the area of South-Urals radioactive plume. Thus, a low effectiveness can be expected in podsolic and leached laterite characterized by a high content of loamy sand and sandy soils, as well as for sobby-podsolic ones. The method can be promising for decontamination of soils and wastes from chemical contaminants, such as Zn, Ni, Cu, Pb, Hg, and others. Important advantages of this method compared to others have been its simplicity, small amount of wastes, and feasibility of decontamination in areas difficult to access. (authors)

Plutonium glove boxes - metrology and operational states

International Nuclear Information System (INIS)

Thyer, A.M.

2001-01-01

The main objective was to undertake a literature review in support of NII's ongoing work in improving safety in the nuclear industry to help define suitable standards of cleanliness for plutonium glove boxes. This is to cover the following areas: existing or proposed national/international standards relating to plutonium glove box cleanliness management; practicable metrology options for assessing the plutonium content of glove boxes; any available dose information relating to the operation of modern and 'old design'; current contamination levels of specific significance (i.e. any accepted level in decommissioning/waste terms, typical criticality limits (if available), any box plutonium loadings that are documented with corresponding operator doses etc.); and, techniques for the decontamination of plutonium glove boxes and their relative effectiveness. This should then form the basis of any further development work undertaken by the UK nuclear industry. Main recommendations are as follows: 1) No information could be found in open literature on acceptable levels of contamination in boxes and action levels for cleanup. If these are not available in closed publications the 2) Where possible, the decontamination methods identified should be tested and dose information recorded against each method to allow informed decisions on which is the optimum technique for a particular form of contamination. 3) Consideration should be given to utilisation of metrology options which have the lowest potential for exposure of operators. Preferred options, may be detection from the outside of boxes using hand-held or permanently located radiation detectors, or semi-intrusive methods such as air-ionisation readings which would require one-off installation of detectors in ductwork

Use of a moving-bed ion-exchange column for plutonium purification; Utilisation d'une colonne echangeuse d'ions a lit mobile pour la purification du plutonium

Energy Technology Data Exchange (ETDEWEB)

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

1965-07-01

When large amounts of fissile matter have to be purified on ion exchange resins, it is difficult to use a fixed bed because of its limiting maximum size. With a moving bed it is possible to ensure a continuous production which can easily be integrated into a purification line on account of its large production capacity. The installation described in this report is derived from an American prototype designed for uranium separation. As a result of many modifications, it is suitable for the purification of plutonium several such columns will shortly be operating in various French centres. The moving bed column, which has a diameter of 25 mm, was first tried with the uranium-thorium mixture; then, after modifications on the plutonium-uranium mixture. The production capacity will depend on the plutonium concentration which can be tolerated in the effluents. It is possible to treat 150 gm/day of plutonium alone; the effluents obtained have a concentration of around of 1 mg/l. The plutonium-uranium separation is improved by a 5 N acidic rinsing as well as by a temperature increase. The decontamination factor increased from 14 in 7 N nitric acid solution to 115 in 5 N nitric acid solution. A temperature increase of about 20 C leads to a decontamination factor of over 500. This result is sufficient encouraging for the possibility of future installations operating in optimum temperature conditions, i.e. 60-65 C, to be considered. (author) [French] Des que l'on desire purifier sur resine echangeuse d'ions des quantites importantes de matieres fissiles, le lit fixe devient difficilement exploitable par suite des dimensions maximum possibles. Le lit mobile permet une production continue pouvant s'integrer facilement par sa capacite de traitement dans une chaine de purification. L'installation decrite dans ce rapport est derivee d'un prototype americain destine a la separation de l'uranium. De nombreuses modifications en font un ensemble utilisable pour la purification du

In-situ dismantling of plutonium-contaminated glove box

International Nuclear Information System (INIS)

Numata, Koji; Watanabe, Hisashi; Ishikawa, Hisashi; Miyo, Hiroaki; Ohtsuka, Katsuyuki

1980-01-01

A plutonium-contaminated glove box was dismantled along with the development of the treatment techniques for plutonium-bearing wastes. The objectives of this in-situ dismantling of the glove box are to reuse the Plutonium Fuel Fabrication Facility more efficiently, to reduce the volume of wastes generated during the dismantling, and to acquire dismantling techniques for decommissioning the Plutonium Fuel Fabrication Facility in the future. Prior to the dismantling works, a greenhouse for decontamination was installed, and the decontamination with surfactants was performed. Unremovable contamination was coated with paint. After this greenhouse was removed, the main greenhouse for dismantling and three greenhouses for contamination control were assembled. The main workers wearing protective devices engaged in dismantling works in the greenhouse. As the protective devices, anorak type PVC suits with air line masks, Howell type pressurized suits, and respirators were used. The tools used for the dismantling are a plasma cutter, an electric nibbler, an electric disk grinder, an electric circular saw and an electric jig saw. The results of the dismantling in-situ were compared with two previous cases of dismantling carried out by different procedures. In the case of in-situ dismantling, the volume of wastes was 1.6 - 1.8 m 3 /m 3 of glove box, and considerable reduction was realized. (Kako, I.)

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

International Nuclear Information System (INIS)

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

2001-01-01

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

Decontamination and reconditioning of the Argonne National Laboratory-West Casting Laboratory alpha glove box

International Nuclear Information System (INIS)

Poston, J.W. Jr.; Burke, L.L.

1998-01-01

The Casting Laboratory (CL) alpha glove box was used to melt and cast metallic uranium and plutonium fuels as part of the Department of Energy''s Liquid Metal Fast Breeder Reactor Program. This highly contaminated alpha glove box was decontaminated and reconditioned to allow a change in mission. The goal of reconditioning was to install experimental apparatus and to improve contamination control prior to introducing plutonium-238 into the CL glove box. Construction of a glove box containment structure and an increase in room ventilation were required. A temporary breathing air station was provided for personnel protection as well as personnel comfort. The historical contamination levels, the decontamination techniques, and the results of decontamination also are presented. The health physics aspects of the CL alpha glove box project may be applicable to other glove box refurbishment or decommissioning projects

An experimental study of the recovery of plutonium from non-combustible wastes

International Nuclear Information System (INIS)

Chamberlain, H.E.; Dalton, J.T.; Dawson, R.K.; Gaudie, S.C.; Turner, A.D.; Wilkins, J.D.

1986-01-01

Removal of loose PuO 2 from non-combustible plutonium contaminated waste by Arklone (1,1,2-trichloro,1,2,2-trifluoro ethane) has been demonstrated on a laboratory scale. While aqueous-containing media are generally more effective decontaminants, Arklone has the advantages of being non-moderating and easily recycled by distillation. Although low-pressure spraying and vibrocleaning are effective contacting methods, ultrasonics gave the highest DF's- reducing residual Pu levels to 1-10 μg/cm 2 . Lower levels are unattainable in a simple batch process due to redeposition of particulates in small surface flaws. More agressive processes are needed to achieve further decontamination. Microscopic smoothness has been identified as the most significant parameter in determining PuO 2 retention and subsequent ease of decontamination. To maintain this, radiation resitance is important, as also is surface hardness under abrasive conditions. For facility walls and ceilings, therefore, electropolished stainless steel, 316L or PEEK foil-faced GRP, and epoxy paint (with fine TiO 2 ) are recommended to reduce residual PuO 2 to 2 after ultrasonic washing, while work-hardened polish rolled stainless steel and bright nickel or chrome electroplates are suggested to achieve similar levels on the floor. 10 tables, 50 figs, 6 refs

An experimental study of the recovery of plutonium from non-combustible wastes

International Nuclear Information System (INIS)

Chamberlain, H.E.; Datton, J.T.; Gaudie, S.C.; Wilkins, J.D.; Dawson, R.K.; Turner, A.D.

1985-12-01

Removal of loose Pu0 2 from non-combustible plutonium contaminated waste by Arklone (1,1,2 trichloro, 1,2,2-trifluoro ethane) has been demonstrated on a laboratory scale. While aqueous containing media are generally more effective decontaminants, Arklone has the advantages of being non-moderating and easily recycled by distillation. Although low pressure spraying and vibrocleaning are effective contacting methods, ultrasonics gave the highest DF's - reducing residual Pu levels to 1-10 μg/cm 2 . Lower levels are unattainable in a simple batch process due to redeposition of particulates in small surface flaws. More aggressive processes are needed to achieve further decontamination - such as paint stripping from mild steel followed by treatment with Marshall's solution ( -4 μCi/cm 2 ), or electrochemical decontamination for stainless steel ( -5 μCi/cm 2 ). Microscopic smoothness has been identified as the most significant parameter in determining Pu0 2 retention and subsequent ease of decontamination. To maintain this, radiation resistance is important, as also is surface hardness under abrasive conditions. For facility walls and ceilings, therefore, electropolished stainless steel, 316L or PEEK foil faced GRP, and epoxy paint (treated with fine Ti0 2 to block any surface defects) are recommended to reduce residual Pu0 2 to 2 after ultrasonic washing, while work-hardened polish rolled stainless steel and bright nickel or chrome electro-plates are suggested to achieve similar levels on the floor. (author)

Soil decontamination criteria report, November 1980

International Nuclear Information System (INIS)

Riordan, G.A.

1980-01-01

A program to access the extent of transuranic soil contamination at DOE sites and to develop methods for their decontamination is underway at Rocky Flats. As part of this program, acceptable soil contamination levels for plutonium proposed by a number of authorities over the past couple of decades were reviewed. From this review, goals for soil decontamination work are proposed. These goals, which relate to the disposition of the products of a decontamination process, are summarized as follows (dpm/g will refer to disintegrations per minute of transuranic nuclides per gram of soil): soil fractions having less than 30 dpm can be disposed of as surface soil with unrestricted usage. Fine soil fractions (less than 100 μm) that have less than 500 dpm and coarse soil fractions that have less than 1000 dpm can be disposed of as subsurface soil as long as usage is controlled to ensure compliance with EPA dosage guidance. Soil concentrates that have an activity greater than the above values but less than 22,000 dpm should be interred in an approved, low level waste burial site. Soil concentrates that are greater than 22,000 dpm should be stored as retrievable waste. Changes in the technical and legal areas of soil decontamination are rapid. Permissible soil decontamination levels will change as will decontamination technology and the ability to monitor the effectiveness of the decontamination processes. As a result, annual updates of decontamination criteria, goals, and monitoring are expected

Decontamination of a plutonium laboratory after a contamination accident

International Nuclear Information System (INIS)

Francioni, W.M.; Haenni, F.

1985-02-01

On the 24th May 1983, a minor explosion occured in a glovebox at the hotlaboratories of the Swiss Federal Institute for Reactor Re-search (EIR). The incident occured during the evaporation of waste slurries associated with the Institute's mixed carbide fuel programme. It resulted in a breaching of the glovebox seals and in heavy contamination of the laboratory housing the box. In this report the problems of decontaminating the laboratory concerned are presented, especially those problems associated with re-contamination during the cleanup process. The experience gained from the decontamination exercise are discussed and details of the costs and resulting quantities of radwaste are also presented. The most important information concerning the incident are also related. (author)

Experience in the cleanup of plutonium-contaminated land

International Nuclear Information System (INIS)

Smith, W.J. II; Fowler, E.B.; Stafford, R.G.

1977-03-01

During the summer of 1974, two accidental releases from a radioactive liquid-waste line at the Los Alamos Scientific Laboratory (LASL) resulted in plutonium contamination of a small area of land, a portion of a Laboratory parking lot, and a strip along an adjacent street. This report documents the immediate control actions and radiation surveys made in response to these leaks, and the subsequent exhumation and decontamination processes, including the physical operations, operational health physics, and soil sample analyses. The cost and results of the decontamination and restoration are also covered

Decontamination and decommissioning assessment for the Waste Incineration Facility (Building 232-Z) Hanford Site, [Hanford], WA

International Nuclear Information System (INIS)

Dean, L.N.

1994-02-01

Building 232-Z is an element of the Plutonium Finishing Plant (PFP) located in the 200 West Area of the Hanford Site. From 1961 until 1972, plutonium-bearing combustible materials were incinerated in the building. Between 1972 and 1983, following shutdown of the incinerator, the facility was used for waste segregation activities. The facility was placed in retired inactive status in 1984 and classified as a Limited Control Facility pursuant to DOE Order 5480.5, Safety of Nuclear Facilities, and 6430.1A, General Design Criteria. The current plutonium inventory within the building is estimated to be approximately 848 grams, the majority of which is retained within the process hood ventilation system. As a contaminated retired facility, Building 232-Z is included in the DOE Surplus Facility Management Program. The objective of this Decontamination and Decommissioning (D ampersand D) assessment is to remove Building 232-Z, thereby elmininating the radiological and environmental hazards associated with the plutonium inventory within the structure. The steps to accomplish the plan objectives are: (1) identifying the locations of the most significant amounts of plutonium, (2) removing residual plutonium, (3) removing and decontaminating remaining building equipment, (4) dismantling the remaining structure, and (5) closing out the project

Decontamination and decommissioning assessment for the Waste Incineration Facility (Building 232-Z) Hanford Site, [Hanford], WA

Energy Technology Data Exchange (ETDEWEB)

Dean, L.N. [Advanced Sciences, Inc., (United States)

1994-02-01

Building 232-Z is an element of the Plutonium Finishing Plant (PFP) located in the 200 West Area of the Hanford Site. From 1961 until 1972, plutonium-bearing combustible materials were incinerated in the building. Between 1972 and 1983, following shutdown of the incinerator, the facility was used for waste segregation activities. The facility was placed in retired inactive status in 1984 and classified as a Limited Control Facility pursuant to DOE Order 5480.5, Safety of Nuclear Facilities, and 6430.1A, General Design Criteria. The current plutonium inventory within the building is estimated to be approximately 848 grams, the majority of which is retained within the process hood ventilation system. As a contaminated retired facility, Building 232-Z is included in the DOE Surplus Facility Management Program. The objective of this Decontamination and Decommissioning (D&D) assessment is to remove Building 232-Z, thereby elmininating the radiological and environmental hazards associated with the plutonium inventory within the structure. The steps to accomplish the plan objectives are: (1) identifying the locations of the most significant amounts of plutonium, (2) removing residual plutonium, (3) removing and decontaminating remaining building equipment, (4) dismantling the remaining structure, and (5) closing out the project.

Evaluation of six decontamination processes on actinide and fission product contamination

International Nuclear Information System (INIS)

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

1995-01-01

In-situ decontamination technologies were evaluated for their ability to: (1) reduce equipment contamination levels to allow either free release of the equipment or land disposal, (2) minimize residues generated by decontamination, and (3) generate residues that are compatible with existing disposal technologies. Six decontamination processes were selected. tested and compared to 4M nitric acid, a traditional decontamination agent: fluoroboric acid (HBF 4 ), nitric plus hydrofluoric acid, alkaline persulfate followed by citric acid plus oxalic acid, silver(II) plus sodium persulfate plus nitric acid, oxalic acid plus hydrogen peroxide plus hydrofluoric acid, and electropolishing using nitric acid electrolyte. The effectiveness of these solutions was tested using prepared 304 stainless steel couponds contaminated with uranium, plutonium, americium, or fission products. The decontamination factor for each of the solutions and tests conditions were determined; the results of these experiments are presented

Electrochemical decontamination system for actinide processing gloveboxes

International Nuclear Information System (INIS)

Wedman, D.E.; Lugo, J.L.; Ford, D.K.; Nelson, T.O.; Trujillo, V.L.; Martinez, H.E.

1998-03-01

An electrolytic decontamination technology has been developed and successfully demonstrated at Los Alamos National Laboratory (LANL) for the decontamination of actinide processing gloveboxes. The technique decontaminates the interior surfaces of stainless steel gloveboxes utilizing a process similar to electropolishing. The decontamination device is compact and transportable allowing it to be placed entirely within the glovebox line. In this way, decontamination does not require the operator to wear any additional personal protective equipment and there is no need for additional air handling or containment systems. Decontamination prior to glovebox decommissioning reduces the potential for worker exposure and environmental releases during the decommissioning, transport, and size reduction procedures which follow. The goal of this effort is to reduce contamination levels of alpha emitting nuclides for a resultant reduction in waste level category from High Level Transuranic (TRU) to low Specific Activity (LSA, less than or equal 100 nCi/g). This reduction in category results in a 95% reduction in disposal and disposition costs for the decontaminated gloveboxes. The resulting contamination levels following decontamination by this method are generally five orders of magnitude below the LSA specification. Additionally, the sodium sulfate based electrolyte utilized in the process is fully recyclable which results in the minimum of secondary waste. The process bas been implemented on seven gloveboxes within LANL's Plutonium Facility at Technical Area 55. Of these gloveboxes, two have been discarded as low level waste items and the remaining five have been reused

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

Electrolytic decontamination of conductive materials for hazardous waste management

International Nuclear Information System (INIS)

Wedman, D.E.; Martinez, H.E.; Nelson, T.O.

1996-01-01

Electrolytic removal of plutonium and americium from stainless steel and uranium surfaces has been demonstrated. Preliminary experiments were performed on the electrochemically based decontamination of type 304L stainless steel in sodium nitrate solutions to better understand the metal removal effects of varying cur-rent density, pH, and nitrate concentration parameters. Material removal rates and changes in surface morphology under these varying conditions are reported. Experimental results indicate that an electropolishing step before contamination removes surface roughness, thereby simplifying later electrolytic decontamination. Sodium nitrate based electrolytic decontamination produced the most uniform stripping of material at low to intermediate pH and at sodium nitrate concentrations of 200 g L -1 and higher. Stirring was also observed to increase the uniformity of the stripping process

Purification and decontamination of a caustic water by reverse osmosis

International Nuclear Information System (INIS)

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

1981-01-01

A reverse osmosis pilot plant was used to decontaminate a caustic water containing low concentrations of uranium, plutonium, and americium. The concentrations of the plutonium and americium were less than one picocurie per liter in the product water. The concentrations of the uranium was reduced to 4.4 picocuries per liter in the product water, which is a reduction of greater than 99%. The reverse osmosis pilot plant was operated at a 98% water recovery, which produced 25,000 gallons per day of product water

Decontamination of stainless steel using cerium(IV): Material recycle and reuse

International Nuclear Information System (INIS)

Kurath, D.E.; Bray, L.A.; Jarrett, J.H.

1997-01-01

It has been demonstrated that the Cerium(IV) process can effectively remove radioactive contamination from stainless steel. Ce(IV) is a powerful oxidizing agent that is applied in an inorganic acid solution or as an atomized spray by injection into steam directed at the contaminated surface. Ce(IV) attacks the oxide layer and underlying metal surface to remove a 0.5-μm to 3-μm layer. This process has been implemented in a number of actual operations. In one application, a Ce(IV) steam decontamination process was instrumental in renovating hot cells at the High-Level Radiochemistry Facility (325-A building) at the Hanford site. The initial dose rate of approximately 100,000 mR/h was reduced to <50 mR/h and allowed manned entry during hot cell renovation activities. These valuable facilities have been returned to full operation. In an application at the West Valley Nuclear Services Co., Inc., the surfaces of stainless steel canisters that had been filled with vitrified high-level waste have been decontaminated. In some cases the free release levels for surface contamination have been achieved. In another application, five plutonium contaminated stainless steel vessels were decontaminated during decommissioning of the Critical Mass Facility at Hanford

Nuclear disaster. Fukushima, hundred years of decontamination; Catastrophe nucleaire: Fukushima, cent ans de decontamination

Energy Technology Data Exchange (ETDEWEB)

Dupin, L.

2011-04-15

This article gives an overview of what will have to be done on the site of Fukushima to decontaminate and to dismantle it. Based on the experience gained in Three Mile Island and in Chernobyl, experts foresee ten years of work within the reactor cores, thirty years around the plant, sixty years of decontamination within the no man's land area around the plant; and centuries as far as scattered spots are concerned more than hundred kilometres away from the plant. Three radionuclides must be surveyed, but with different half lives: iodine 131 (8 days), caesium 137 (30 years), and plutonium 239 (24000 years). The expertise of French companies (Areva, Assystem, Bouygues and Vinci) in reactor dismantling, dismantling procedure design, and public works (protection arch like in Chernobyl) is briefly evoked, as well as the French approach for post-accident management

The Creative Application of Science, Technology and Work Force Innovations to the Decontamination and Decommissioning of the Plutonium Finishing Plant at the Hanford Nuclear Reservation

International Nuclear Information System (INIS)

Charboneau, S.; Klos, B.; Heineman, R.; Skeels, B.; Hopkins, A.

2006-01-01

The Plutonium Finishing Plant (PFP) consists of a number of process and support buildings for handling plutonium. Building construction began in the late 1940's to meet national priorities and became operational in 1950 producing refined plutonium salts and metal for the United States nuclear weapons program The primary mission of the PFP was to provide plutonium used as special nuclear material for fabrication into a nuclear device for the war effort. Subsequent to the end of World War II, the PFP's mission expanded to support the Cold War effort through plutonium production during the nuclear arms race. PFP has now completed its mission and is fully engaged in deactivation, decontamination and decommissioning (D and D). At this time the PFP buildings are planned to be reduced to ground level (slab-on-grade) and the site remediated to satisfy national, Department of Energy (DOE) and Washington state requirements. The D and D of a highly contaminated plutonium processing facility presents a plethora of challenges. PFP personnel approached the D and D mission with a can-do attitude. They went into D and D knowing they were facing a lot of challenges and unknowns. There were concerns about the configuration control associated with drawings of these old process facilities. There were unknowns regarding the location of electrical lines and the condition and contents of process piping containing chemical residues such as strong acids and caustics. The gloveboxes were highly contaminated with plutonium and chemical residues. Most of the glovebox windows were opaque with splashed process chemicals that coated the windows or etched them, reducing visibility to near zero. Visibility into the glovebox was a serious worker concern. Additionally, all the gloves in the gloveboxes were degraded and unusable. Replacing gloves in gloveboxes was necessary to even begin glovebox clean-out. The sheer volume of breathing air needed was also an issue. These and other challenges and PFP

Passive neutron survey of the 233-S Plutonium Concentration Facility

International Nuclear Information System (INIS)

1996-08-01

A passive neutron survey was performed at the 233-S Plutonium Concentration Facility (located at the Hanford Site in Richland, Washington) during late 1994 and early 1995. Four areas were surveyed: an abandoned filter box and pipe trench, column laydown trench, load-out hood, and process hood. The primary purpose of the survey was to identify locations that had plutonium to help direct decontamination and decommissioning activities. A secondary purpose of the survey was to determine the quantity of material when its presence was identified

Decontamination of material in the Marcoule plutonium producing centre (1961)

International Nuclear Information System (INIS)

Rodier, J.; Bouzigues, H.; Boutot, P.

1961-01-01

The decontamination of material in an atomic centre is an essential operation in view of the cost and the difficulties of replacement. It also makes it possible to reduce the storage of radio-active materials always an expensive task. Surfaces are contaminated by retention of radioactive products and the mechanism of the bounding forces can be explained in terms of chemical, mechanical, electrostatic and surface tension phenomena. The methods used for decontamination are either physical (section, abrasion, steam, ultrasonics) or chemical (acids, alkalis, detergents, reducing and oxidising agents). At Marcoule, chemical methods of treatment are used. This is effected in tanks, the exact composition of the liquids being regulated from a control panel. Working experience has shown that the fact of operating in humid conditions eliminates all problems of atmospheric contamination; as a result it is possible for the personnel to work without any special protective devices. Almost all the material can be re-utilized and the operations produce only a small volume of liquid waste. The decontamination workshop is operated by a small number of workers. The working costs, including capital repayment and treatment of the waste, do not exceed 15 per cent of the value of the apparatus treated. (authors) [fr

Achievement and future plan on plutonium use in Japan

International Nuclear Information System (INIS)

Uematsu, Kunihiko

1998-05-01

The plutonium recycle option has been supported from the early stage of nuclear development by Japanese Government because of the very weak structure of energy supplying system. Power Reactor and Nuclear Fuel Development Corporation (PNC) has been developing the plutonium recycling technology such as fast breeder reactor, MOX fuel fabrication and reprocessing technologies based on the decision of the government. The paper describes the obtained result of technical development and the future R and D program in the field of plutonium recycle. (J.P.N.)

Decontamination of material in the Marcoule plutonium producing centre (1961); La decontamination du materiel dans le centre de production du plutonium de Marcoule (1961)

Energy Technology Data Exchange (ETDEWEB)

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

1961-07-01

The decontamination of material in an atomic centre is an essential operation in view of the cost and the difficulties of replacement. It also makes it possible to reduce the storage of radio-active materials always an expensive task. Surfaces are contaminated by retention of radioactive products and the mechanism of the bounding forces can be explained in terms of chemical, mechanical, electrostatic and surface tension phenomena. The methods used for decontamination are either physical (section, abrasion, steam, ultrasonics) or chemical (acids, alkalis, detergents, reducing and oxidising agents). At Marcoule, chemical methods of treatment are used. This is effected in tanks, the exact composition of the liquids being regulated from a control panel. Working experience has shown that the fact of operating in humid conditions eliminates all problems of atmospheric contamination; as a result it is possible for the personnel to work without any special protective devices. Almost all the material can be re-utilized and the operations produce only a small volume of liquid waste. The decontamination workshop is operated by a small number of workers. The working costs, including capital repayment and treatment of the waste, do not exceed 15 per cent of the value of the apparatus treated. (authors) [French] La decontamination du materiel dans un centre atomique est une operation indispensable etant donne le cout et les difficultes du remplacement. Elle contribue aussi a diminuer les stockages toujours onereux des materiaux radioactifs. Les surfaces se contaminent par retention de corps radioactifs, l'origine des forces de liaison devant etre recherchee dans les phenomenes chimiques, mecaniques, electro-statiques ou de tensions superficielles. Les methodes de decontamination peuvent etre physiques (aspiration, abrasion, vapeur, ultra-sons) ou chimiques (acides, alcalins, detergents, reducteurs, oxydants). Sur le centre de Marcoule, la methode des traitements chimiques a ete

Demonstration and evaluation of the CORPEX trademark Nuclear Decontamination Process, Technical task plan No. SR152005. Final Report

International Nuclear Information System (INIS)

May, C.G.

1997-01-01

In June, 1995, the Decontamination and Decommissioning Focus Area funded a demonstration of the CORPEX Nuclear Decontamination Process in an Old Metallography Laboratory glovebox at the Savannah River Site. The objective of the demonstration was to prove the effectiveness of a new and innovative technology that would reduce the risks associated with future cleanups of plutonium-238 contaminated equipment in the DOE complex. After facility and vendor preparations in support of the demonstration, Westinghouse Savannah River Company (WSRC) was informed by the vendor that the chemistry proposed for use in the decontamination process was not effective on sintered plutonium, which was the form of plutonium in the selected glovebox. After further technical evaluation, the demonstration was canceled. This report describes the work performed in support of the demonstration and the present status of the project. The CORPEX chemical process is a nondestructive cleaning method that removes only the contaminant and the matrix that fixed the contaminant to the surface. It does not damage the substrate. The cleaning agent is destroyed by the addition of proprietary oxidizers, leaving water, carbon dioxide and nitrogen gases, and a sludge as waste

Full system decontamination. AREVAs experience in decontamination prior to decommissioning

International Nuclear Information System (INIS)

Topf, Christian

2010-01-01

Minimizing collective radiation exposure and producing free-release material are two of the highest priorities in the decommissioning of a Nuclear Power Plant (NPP). Full System Decontamination (FSD) is the most effective measure to reduce source term and remove oxide layer contamination within the plant systems. FSD is typically a decontamination of the primary coolant circuit and the auxiliary systems. In recent years AREVA NP has performed several FSDs in PWRs and BWRs prior to decommissioning by applying the proprietary CORD copyright family and AMDA copyright technology. Chemical Oxidation Reduction Decontamination or CORD represents the chemical decontamination process while AMDA stands for Automated Mobile Decontamination Appliance, AREVA NPs decontamination equipment. Described herein are the excellent results achieved for the FSDs applied at the German PWRs Stade in 2004 and Obrigheim in 2007 and for the FSDs performed at the Swedish BWRs, Barsebaeck Unit 1 in 2007 and Barsebaeck Unit 2 in 2008. All four FSDs were performed using the AREVA NP CORD family decontamination technology in combination with the AREVA NP decontamination equipment, AMDA. (orig.)

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

International Nuclear Information System (INIS)

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

1983-11-01

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

Recovery of americium-241 from aged plutonium metal

International Nuclear Information System (INIS)

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

1980-12-01

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

Comparative scrub solution tests for decontamination of transuranic radionuclides from soils

International Nuclear Information System (INIS)

Stevens, J.R.; Kochen, R.L.; Rutherford, D.W.; Riordan, G.A.; Delaney, I.C.

1982-08-01

Soil decontamination tests were done using three scrubbing solutions on five different transuranic-contaminated soils from Department of Energy sites. The soils came from Rocky Flats, Colorado; Hanford, Washington; Mound Facility, Ohio; Idaho National Engineering Laboratory, Idaho; and Los Alamos National Laboratory, New Mexico. Decontamination was effected by physical and chemical means. A pH 12.5 scrub effected decontamination by serving as a hydraulic grading and attrition scrub medium; this solution did not solubilize the actinide contamination. A 2% HNO 3 , 0.2% HF, 2% pine oil, and 5% Calgon solution effected decontamination by physical and chemical means; this solution solubilized particulate actinide and actinide dispersed on the surface of soil particles. A 2N HCl scrub was also used to effect decontamination by physical and chemical means; this reagent solubilized soil constituents, removing contamination that had migrated into mineral surfaces. Only Rocky Flats soil was effectively decontaminated by the high pH solution although all soils had an enrichment of the activity in the -150 mesh fraction. Attrition scrubbing with both acid solutions had a better decontamination ability for the +150 mesh fraction for Hanford, INEL, and LANL soils. In addition, the acid solutions solubilized some of the plutonium and had a decontamination effect on the fine fractions

Development and assessment of two decontamination processes: closed electropolishing system for decontamination of underwater surfaces -vibratory decontamination with abrasives

International Nuclear Information System (INIS)

Benavides, E.; Fajardo, M.

1992-01-01

Two decontamination processes have been developed to decontaminate the stainless steel components of nuclear power plants. The first process uses an underwater closed electropolishing system for the decontamination of large stainless steel surfaces in flooded systems without loss of electrolyte. Large underwater contaminated areas can be treated with an electropolishing head covering an area of 2 m 2 in one step. The decontamination factors achieved with this technique range between 100 and 1000. The second process consists in the decontamination of nuclear components using vibratory equipment with self-cleaning abrasives generating a minimum quantity of waste. This technique may reach contamination factors similar to those obtained with other abrasive methods (brush abrasion, abrasive blasting, etc...). The obtained decontamination factors range between 5 and 50. Only a small quantity of waste is generated, which is treated and reduced in volume by filtration and evaporation

Low-waste electrochemical decontamination of stainless-steel surface

International Nuclear Information System (INIS)

Babain, V.A.; Smirnov, I.V.; Shadrin, A.Yu.; Firsin, N.G.; Zakharchuk, G.A.; Pavlov, A.B.; Shilov, V.V.

2002-01-01

An electrochemical decontamination method using a formic acid-based recycling electrolyte was proposed to remove firmly fixed contaminants from stainless-steel surfaces. The following provisions make for minimisation of the amounts of waste: (i) use of specially designed electrodes with vacuum removal of spent electrolyte; (ii) inter-cycle removal of radionuclides from the electrolyte by using an inorganic sorbent; (iii) periodic regeneration of the spent electrolyte. the dissolved metals (Fe, Cr, Ni) being transformed into acidic phosphates; (iv) solidification of residues arising from the regeneration of the electrolyte and spent sorbent into iron-phosphate ceramics. The technology and equipment developed were used for decontamination of a plutonium glove-box. The level of surface contamination was reduced 100-fold in two decontamination cycles. The depth of metal skimming was 1.5 μ for the ceiling and walls and 4.5 μ for the table top. Each square meter of stainless-steel surface provides about 100 g of solid radioactive waste in the form of iron-phosphate ceramic blocks

Preliminary laboratory study of plutonium-238 dissolution from Mound soil by means of the ACT*DE*CONSM process

International Nuclear Information System (INIS)

Brown, K.A.; Heinrich, R.R.; Johnson, D.O.; Edgar, D.E.

1992-04-01

The treatment of contaminated soil presents a significant technical problem. Soil-washing and chemical-extraction methods have proven to be effective for specific applications, but a process with more comprehensive treatment properties that is both cost-effective and environmentally propitious is needed. Bradtec, Inc., has developed a process, the ACT*DE*CON SM process, that has been tested on soil contaminated with plutonium. The process effectively extracted Pu-238 after three washes, reducing the contamination levels from approximately 20 Bq/g to 1.6--1.9 Bq/g and yielding a decontamination factor ranging from 11 to 13. By using four or more ACT*DE*CON SM washes or a continuous-flow process with ACT*DE*CON SM solvents on a pilot-scale test, a target decontamination level of 0.93 Bq/g might be achievable

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

Energy Technology Data Exchange (ETDEWEB)

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

1997-12-01

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

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

International Nuclear Information System (INIS)

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

1997-01-01

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

The decontamination of a pressurised suit area at AEE Winfrith. Part 1

International Nuclear Information System (INIS)

Bond, R.D.; Rankin, J.D.; Robinson, D.H.; Sanders, M.J.

1984-04-01

Dry suction cleaning and chemical foam treatment were used on a plutonium oxide decontaminated area. Details of the equipment and reagents are given together with the results. Average levels of contamination by one application were reduced by over 80 percent, and airborne levels by more than 99 percent. (U.K.)

Decontamination of main coolant pumps

International Nuclear Information System (INIS)

Roofthooft, R.

1988-01-01

Last year a number of main coolant pumps in Belgian nuclear power plants were decontaminated. A new method has been developed to reduce the time taken for decontamination and the volume of waste to be treated. The method comprises two phases: Oxidation with permanganate in nitric acid and dissolution in oxalic acid. The decontamination of main coolant pumps can now be achieved in less than one day. The decontamination factors attained range between 15 and 150. (orig.) [de

Cleanup and treatment (CAT) test: a land-area decontamination project utilizing a vacuum method of soil removal

International Nuclear Information System (INIS)

Orcutt, J.A.

1982-08-01

Areas 11 and 13 of the Nevada Test Site (NTS) are contaminated with varying concentrations of Pu-239, 240 and Am-241. An investigation of a vacuum method of soil removal, the Cleanup and Treatment (CAT) test, was conducted over a 3-month period in the plutonium safety shot or Plutonium Valley portion of Area 11. Soil in Plutonium Valley is of the Aridisol Order. The surface 0 to 10 cm is a gravelly loam, and is strongly alkaline (pH 8.8). A large truck-mounted vacuum unit, rather than conventional earth-moving equipment, was used as the primary soil collection unit. Effectiveness of the vacuum method of soil removal was evaluated in relation to conventional earthmoving procedures, particularly in terms of volume reduction of removed soil achieved over conventional techniques. Radiological safety considerations associated with use of the vacuum unit were evaluated in relation to their impact on a full-scale land decontamination program. Environmental and operational impacts of devegetation with retention of root crowns or root systems were investigated. It is concluded that the CAT test was successful under difficult environmental conditions

The medical treatment of the plutonium-contaminated wound

International Nuclear Information System (INIS)

Liu Yanling

1988-01-01

Some experiences in medical treatment of plutonium-contaminated wound gained through the animal experiments and clinical practices were described. For the treatment of plutonium-contaminated wound, much attention should be devoted to the early emergency measure at accident site. In some case when the surgical interference is needed, radioactivity in local wound and in regional lympho-nodes of wound, firstly, must be determined and the contaminated area must be demonstrated before operation. Selecting a proper approach for anaesthesia is one of the critical factors for successfulness of operation. The operation should be performed under the coordination of monitoring workers. During operation, the rules for decontamination should be followed to avoid recontamination. In addition to conventional administration of chelating agents, the local application of such agents during and after operation is a better supplementary therapeutic procedure for some cases when the residual amount of plutonium in wound is less and any other surgical procedures will not be performed further

Magnetic separation for soil decontamination

International Nuclear Information System (INIS)

Avens, L.R.; Worl, L.A.; deAguero, K.J.; Padilla, D.D.; Prenger, F.C.; Stewart, W.F.; Hill, D.D.; Tolt, T.L.

1993-01-01

High gradient magnetic separation (HGMS) is a physical separation process that is used to extract magnetic particles from mixtures. The technology is used on a large scale in the kaolin clay industry to whiten or brighten kaolin clay and increase its value. Because all uranium and plutonium compounds are slightly magnetic, HGMS can be used to separate these contaminants from non-magnetic soils. A Cooperative Research and Development Agreement (CRADA) was signed in 1992 between Los Alamos National Laboratory (LANL) and Lockheed Environmental Systems and Technologies Company (LESAT) to develop HGMS for soil decontamination. This paper reports progress and describes the HGMS technology

Precipitation of plutonium oxalate from homogeneous solutions

International Nuclear Information System (INIS)

Rao, V.K.; Pius, I.C.; Subbarao, M.; Chinnusamy, A.; Natarajan, P.R.

1986-01-01

A method for the precipitation of plutonium(IV) oxalate from homogeneous solutions using diethyl oxalate is reported. The precipitate obtained is crystalline and easily filterable with yields in the range of 92-98% for precipitations involving a few mg to g quantities of plutonium. Decontamination factors for common impurities such as U(VI), Am(III) and Fe(III) were determined. TGA and chemical analysis of the compound indicate its composition as Pu(Csub(2)Osub(4))sub(2).6Hsub(2)O. Data are obtained on the solubility of the oxalate in nitric acid and in mixtures of nitric acid and oxalic acid of varying concentrations. Green PuOsub(2) obtained by calcination of the oxalate has specifications within the recommended values for trace foreign substances such as chlorine, fluorine, carbon and nitrogen. (author)

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.

Glovebox decontamination technology comparison

International Nuclear Information System (INIS)

Quintana, D.M.; Rodriguez, J.B.; Cournoyer, M.E.

1999-01-01

Reconfiguration of the CMR Building and TA-55 Plutonium Facility for mission requirements will require the disposal or recycle of 200--300 gloveboxes or open front hoods. These gloveboxes and open front hoods must be decontaminated to meet discharge limits for Low Level Waste. Gloveboxes and open front hoods at CMR have been painted. One of the deliverables on this project is to identify the best method for stripping the paint from large numbers of gloveboxes. Four methods being considered are the following: conventional paint stripping, dry ice pellets, strippable coatings, and high pressure water technology. The advantages of each technology will be discussed. Last, cost comparisons between the technologies will be presented

Lixiviation of plutonium contaminated solid wastes by aqueous solution of electro-generated reducing agents

International Nuclear Information System (INIS)

Agarande, Michelle

1991-01-01

This study concerns the development of the new concept for the decontamination of plutonium bearing solid wastes, based on the lixiviation of the wastes using electro-generated reducing agents. First, a comparative study of the kinetics of the dissolution of pure PuO 2 (prepared by calcination of Pu (IV) oxalate at 450 C) in sulfuric acid media, with different reducing agents, was realized. Qualitatively these reagents can be sorted in three groups: 1 / fast kinetics for Cr(II), V(II) and U(III); 2 / slow kinetics for Ti(III); 3 / very slow kinetics for V(III) and U(VI). In order to contribute to the design of an electrochemical reactor for the generation of the reducing agents usable for the lixiviation of plutonium bearing solid wastes, the study of the diffusion coefficients of both oxidized and reduced forms of different redox couples, at different temperatures, was undertaken. The results of this study also permits, from the knowledge of the diffusional activation energy of the ions, to conclude that the dissolution of pure plutonium dioxide under the action of these reducing agents is not diffusion limited. The feasibility of the plutonium decontamination treatment of synthetic or real solid wastes was then studied at laboratory scale using electro-generated V(II), which is with Cr(II) among the best reagents. The efficiency of the treatment was good, (80 pc Pu solubilisation yield), especially in the case of cellulosic or miscellaneous organic wastes. (author) [fr

Guide of good practices for occupational radiological protection in plutonium facilities

Energy Technology Data Exchange (ETDEWEB)

NONE

1998-06-01

This Technical Standard (TS) does not contain any new requirements. Its purpose is to provide guides to good practice, update existing reference material, and discuss practical lessons learned relevant to the safe handling of plutonium. the technical rationale is given to allow US Department of Energy (DOE) health physicists to adapt the recommendations to similar situations throughout the DOE complex. Generally, DOE contractor health physicists will be responsible to implement radiation protection activities at DOE facilities and DOE health physicists will be responsible for oversight of those activities. This guidance is meant to be useful for both efforts. This TS replaces PNL-6534, Health Physics Manual of Good Practices for Plutonium Facilities, by providing more complete and current information and by emphasizing the situations that are typical of DOE`s current plutonium operations; safe storage, decontamination, and decommissioning (environmental restoration); and weapons disassembly.

ALARA review for the decontamination and decommissioning of the 233-S pipe trench

International Nuclear Information System (INIS)

Kornish, M.J.

1998-01-01

The 233-S Facility was completed in 1955 to expand plutonium production by further concentrating the plutonium nitrate product solution from the Reduction Oxidation (REDOX) Plant. The facility is radiologically contaminated because of operations and accidents. Isolation from REDOX and removal of the product transfer lines from the pipe trench is the second step in the decontamination and decommissioning of the entire 233-S Facility. The work scope is to isolate all piping from REDOX and then to remove all the piping/equipment from the pipe trench. The building is presently a Hazard Category 2 Nuclear Facility. A formal as low as reasonably achievable (ALARA) review is required by BHI-SH-02, Vol. 1, Procedure No. 1.22, Planning Radiological Work, when radiological conditions exceed trigger levels. The level of contamination inside the pipe trench and the process fluid piping is unknown. The potential exists to exceed the level of loose surface contamination, which requires a formal ALARA review when opening the pipe trench and cutting of piping commences. This ALARA review is for task instruction 1997-03-18-009 Revision 1, 233-S Pipe Trench Decon and Pipe Removal

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

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

International Nuclear Information System (INIS)

Saulze, J.L.

1990-01-01

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

Summary review of Mound Facility's experience in decontamination of concrete

International Nuclear Information System (INIS)

Combs, A.B.; Davis, W.P.; Garner, J.M.; Geichman, J.R.

1980-01-01

Most of the current concrete decontamination work at Mound Facility involves surfaces that are contaminated with plutonium-238. Approximately 60,000 sq. ft. of concrete floors will have to be decontaminated in Mound's current Decontamination and Decommissioning (D and D) Project. Although most of these surfaces are partially protected by a barrier (tile or paint), contaminated water and acid have penetrated these barriers. The technique for decontaminating these floors is desribed. The initial cleaning of the floor involes standard water and detergent. Acids are not used in cleaning as they tend to drive the contamination deeper into the concrete surface. Next, the floor tile is manually removed inside a temporary enclosure under negative and filtered ventilation. Finally, layers of contaminated concrete are mechanically removed inside the ventilated enclosure. The suspected depth and surface area of contamination determines the type of mechanical tool used. In summary, several generic methods of concrete decontamination can be utilized: chemical, such as water, detergent, acids, paint remover, strippable paints, etc.; rotary using sanders, grinders, scarifiers, etc.; impact such as pressure washers (hydrolasers), particle blasters, scabblers, needlers, spallers, paving and rock breakers, ram hoes, etc. The particular method used depends on several factors: surface and area involved; depth of contamination; cost and availability of equipment; usage safety and radiological control; and waste generated

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)

Removal of sulfamic acid from plutonium sulfamate--sulfamic acid solution

International Nuclear Information System (INIS)

Gray, L.W.

1978-10-01

Plutonium metal can be readily dissolved in aqueous solutions of sulfamic acid. When the plutonium sulfamate--sulfamic acid solutions are added to normal purex process streams, the sulfamate ion is oxidized by addition of sodium nitrite. This generates sodium sulfate which must be stored as radioactive waste. When recovery of ingrown 241 Am or storage of the dissolved plutonium must be considered, the sulfamate ion poses major and undesirable precipitation problems in the process streams. The present studies show that 40 to 80% of the sulfamate present in the dissolver solutions can be removed by precipitation as sulfamic acid by the addition of concentrated nitric acid. Addition of 64% nitric acid allows precipitation of 40 to 50% of the sulfamate; addition of 72% nitric acid allows precipitation of 50 to 60% of the sulfamate. If the solutions are chilled, additional sulfamic acid will precipitate. If the solutions are chilled to -10 0 C, about 70 to 80% of the orginal sulfamic acid in the dissolver will precipitate. A single, low-volume wash of the sulfamic acid crystals with concentrated nitric acid will decontaminate the crystals to a plutonium content of 5 dis/(min-gram)

Decontamination of TRU glove boxes

International Nuclear Information System (INIS)

Crawford, J.H.

1978-03-01

Two glove boxes that had been used for work with transuranic nuclides (TRU) for about 12 years were decontaminated in a test program to collect data for developing a decontamination facility for large equipment highly contaminated with alpha emitters. A simple chemical technique consisting of a cycle of water flushes and alkaline permanganate and oxalic acid washes was used for both boxes. The test showed that glove boxes and similar equipment that are grossly contaminated with transuranic nuclides can be decontaminated to the current DIE nonretrievable disposal guide of <10 nCi TRU/g with a moderate amount of decontamination solution and manpower. Decontamination of the first box from an estimated 1.3 Ci to about 5 mCi (6 nCi/g) required 1.3 gallons of decontamination solution and 0.03 man-hour of work for each square foot of surface area. The second box was decontaminated from an estimated 3.4 Ci to about 2.8 mCi (4.2 nCi/g) using 0.9 gallon of decontamination solution and 0.02 man-hour for each square foot of surface area. Further reductions in contamination were achieved by repetitive decontamination cycles, but the effectiveness of the technique decreased sharply after the initial cycle

The Plutonium Fuel Laboratory at Studsvik and Its Activities

Energy Technology Data Exchange (ETDEWEB)

Hultgren, A.; Berggren, G.; Brown, A.; Eng, H. U.; Forsyth, R. S. [AB Atomenergi, Studsvik (Sweden)

1967-09-15

The plutonium fuel laboratory at Studsvik is engaged in development work on plutonium-enriched fuel. At present, low enriched fuel for thermal reactors is being studied: work on fuel with a higher plutonium content for fast reactors is foreseen at a later date. So far only the pellet technique is under consideration, and a number of pellet rod specimens will be produced and irradiated in the reactor R2. These specimens include pellets from both co-precipitated uranium-plutonium salts and from physically mixed oxides. Comparison of these two materials will be extended to different density levels and different heat ratings. The methods and techniques used and studied include wet chemical work for powder preparation (continuous precipitation of Pu(IV)-oxalate with oxalic acid, continuous co-precipitation of plutonium and uranium with ammonia, optimization of.precipitation conditions using U(IV) and U(VI) respectively) ; powder preparation (drying, calcination, reduction, mixing, milling, binder addition, granulation); pellet preparation (pressing, debonding, sintering, inspection): encapsulation (charging, welding of end plug, helium filling, end sealing by welding, leak detection, decontamination); metallography (specimen preparation (moulding, polishing), etching, microscopy); structure investigations (thermal analysis (TG, DTA), X-ray diffraction, neutron diffraction, data handling by computer analysis); radiometric methods (direct plutonium determination by gamma spectrometry, non-destructive burn-up analysis by high resolution gamma spectrometry, using a Ge(Li) detector) ; rework of waste (recovery of plutonium from fuel waste by extraction with trilauryl amine and anion exchange). The plutonium fuel laboratory forms part of the Active Central Laboratory. The equipment is contained in four adjacent 10 x 15 m rooms; .for diffraction work and inactive uranium work additional space is available. All the forty glove boxes in operation except two are of AB Atomenergi

Decommissioning and Decontamination

International Nuclear Information System (INIS)

Massaut, V.

2000-01-01

The objectives of SCK-CEN's decommissioning and decontamination programme are (1) to develop, test and optimise the technologies and procedures for decommissioning and decontamination of nuclear installations in order to minimise the waste arising and the distributed dose; (2) to optimise the environmental impact; (3) to reduce the cost of the end-of-life of the installation; (4) to make these new techniques available to the industry; (5) to share skills and competences. The programme and achievements in 1999 are summarised

Reactor component chemical decontamination-developments in waste handling and disposal

International Nuclear Information System (INIS)

Papesch, R.; Atwood, K.L.

1989-01-01

Because of restrictive limits on man-rem exposure in European nuclear plants, a company has developed and applied a number of chemical decontamination techniques for components that must be periodically maintained. These techniques are particularly effective for components that can be placed in a decontamination bath for dose reduction prior to performing maintenance. The cleaning technique has the ability to achieve decontamination factors of at least 20 and in some cases much greater. For components with before cleaning dose rates of between 1 to as high as 80 R/hr, significant man-rem reductions are achieved when hundreds of manhours may be required to complete required component maintenance. Transferring this solvent technology to the U.S. required a program to develop solidification formulas to allow the solvent wastes to be disposed of in accordance with regulations and in a cost effective manner. This paper demonstrates in chemical decontaminations with small liquid volume systems that concentrated decontamination solvents can be employed to achieve high decontamination factors

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

Electrolytic decontamination of the 3013 inner can

International Nuclear Information System (INIS)

Wedman, D.E.; Nelson, T.O.; Rivera, Y.; Weisbrod, K.; Martinez, H.E.; Limback, S.

1998-01-01

Disposition of plutonium recovered from nuclear weapons or production residues must be stored in a manner that ensures safety. The criteria that has been established to assure the safety of stored materials for a minimum of 50 years is DOE-STD-3013. Los Alamos National Laboratory (LANL) has designed a containment package in accordance with the DOE standard. The package consists of an optional convenience (food pack) can, a welded type 304L stainless steel inner (primary) can, and a welded type 304L stainless steel outer (secondary) can. With or without the food pack can, the material is placed inside the primary can and welded shut under a helium atmosphere. This activity takes place totally within the confinement of the glove box line. Following the welding process, the can is checked for leaks and then sent down the line for decontamination. Once decontaminated, the sealed primary can may be removed from the glove box line. Welding of the secondary container takes place outside the glove box line. The highly automated decontamination process that has been developed to support the packaging of Special Nuclear Materials is based on an electrolytic process similar to the wide spread industrial technique of electropolishing. The can is placed within a specially designed stainless steel fixture built within a partition of a glove box. This fixture is then filled with a flowing electrolyte solution. A low DC electric current is made to flow between the can, acting as the anode, and the fixture, acting as the cathode. Following the decontamination, the system provides a flow of rinse water through the fixture to rinse the can of remaining salt residues. The system then carried out a drying cycle. Finally, the fixture is opened from the opposite side of the partition and the can surface monitored directly and through surface smears to assure that decontamination is adequate

Electrolytic decontamination of the 3013 inner can

International Nuclear Information System (INIS)

Wedman, D.E.; Nelson, T.O.; Rivera, Y.; Weisbrod, K.; Martinez, H.E.; Limback, S.

1998-01-01

Disposition of plutonium recovered from nuclear weapons or production residues must be stored in a manner that ensures safety. The criteria that has been established to assure the safety of stored materials for a minimum of 50 years is DOE-STD-3013. This standard specifies both the requirements for containment and furthermore specifies that the inner container be decontaminated to a level of ≤20 dpm/100 cm 2 swipable and ≤500 dpm/100 cm 2 direct alpha such that a failure of the outer containment barrier will have a lower probability of resulting in a spread of contamination. The package consists of an optional convenience (food pack) can, a welded type 304L stainless steel inner (primary) can, and a welded type 304L stainless steel outer (secondary) can. Following the welding process, the can is checked for leaks and then sent down the line for decontamination. Once decontaminated, the sealed primary can may be removed from the glove box line. Welding of the secondary container takes place outside the glove box line. The highly automated decontamination process that has been developed to support the packaging of Special Nuclear Materials is based on an electrolytic process similar to the wide spread industrial technique of electropolishing. The can is placed within a specially designed stainless steel fixture built within a partition of a glove box. The passage of current through this electrolytic cell results in a uniform anodic dissolution of the surface metal layers of the can. This process results in a rapid decontamination of the can. The electrolyte is fully recyclable, and the separation of the chromium from the actinides results in a compact, non RCRA secondary waste product

Plutonium solution in concentration range from 8 to 17 G/liter

Energy Technology Data Exchange (ETDEWEB)

Rothe, R.E.

1997-06-01

This paper very briefly discusses the need for a fundamental criticality study of low concentrations of plutonium solutions. Examples of the occurrence of such solutions, which are characteristic of waste, are cited. Due to the prevalence of decontaminating and decommissioning activities, low concentration solutions are expected to become an important concern. Technical deficiencies in previous calculations are also discussed as a reason for performing low concentration criticality studies. 3 refs.

Plutonium solution in concentration range from 8 to 17 G/liter

International Nuclear Information System (INIS)

Rothe, R.E.

1997-01-01

This paper very briefly discusses the need for a fundamental criticality study of low concentrations of plutonium solutions. Examples of the occurrence of such solutions, which are characteristic of waste, are cited. Due to the prevalence of decontaminating and decommissioning activities, low concentration solutions are expected to become an important concern. Technical deficiencies in previous calculations are also discussed as a reason for performing low concentration criticality studies. 3 refs

Experiences in the management of plutonium-containing solid-wastes at the Nuclear Research Center Karlsruhe

International Nuclear Information System (INIS)

Baehr, W.; Hild, W.; Scheffler, K.

1974-10-01

Solid-plutonium-containing wastes from a fuel production plant, a reprocessing plant and several research laboratories are treated at the decontamination department of the Karlsruhe Nuclear Research Center for disposal in the Asse salt mine. Conditioning as well as future aspects in α-waste management are the subject of this Paper. (orig.) [de

Criticality evaluation for the 233-S decontamination and decommissioning project

International Nuclear Information System (INIS)

1996-08-01

This criticality evaluation document analyzes the potential of a criticality event as a result of decontaminating and decommissioning the 233-S Plutonium Concentration Facility. These calculations supplement the previous set of calculations performed under this same contract, which were performed on March 13, 1996. These calculations were performed using the same MCNP computer code as for the previous set; the validation calculations performed then are valid for this set as well. Hand calculations, using the method of Solid Angle, were also developed

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

Energy Technology Data Exchange (ETDEWEB)

ULLAH, M K

2001-02-26

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

Vacuum distillation of plutonium pyrochemical salts

International Nuclear Information System (INIS)

Bourges, Gilles; Faure, S.; Fiers, B.; Saintignon, S.; Lemoine, O.; Cardona-Barrau, D.; Devillard, D.

2012-01-01

A pyrochemical process is developed to upgrade the safety of plutonium spent salts interim storage. The feed material, consisting of alkali or alkali-earth chlorides containing various Pu and Am species, is first oxidized to convert the actinides into oxides. Then the chlorides are removed by vacuum distillation which requires temperature from 750 degrees C to 1100 degrees C. After a comprehensive R and D program, full-scale equipment was built to test the distillation of active salts. Tests with NaCl/KCl oxidized spent salt give decontamination factor of chlorides higher than 20000. The distilled salt meets the radiologic requirements to be discarded as low level waste. (authors)

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)

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)

Properties and solidification of decontamination wastes

International Nuclear Information System (INIS)

Davis, M.S.; Piciulo, P.L.; Bowerman, B.S.; Adams, J.W.; Milian, L.

1983-01-01

LWRs will require one or more chemical decontaminations to achieve their designed lifetimes. Primary system decontamination is designed to lower radiation fields in areas where plant maintenance personnel must work. Chemical decontamination methods are either hard (concentrated chemicals, approximately 5 to 25 weight percent) or soft (dilute chemicals less than 1 percent by weight). These methods may have different chemical reagents, some tailor-made to the crud composition and many methods are and will be proprietary. One factor common to most commercially available processes is the presence of organic acids and chelates. These types of organic reagents are known to enhance the migration of radionuclides after disposal in a shallow land burial site. The NRC sponsors two programs at Brookhaven National Laboratory that are concerned with the management of decontamination wastes which will be generated by the full system decontamination of LWRs. These two programs focus on potential methods for degrading or converting decontamination wastes to more acceptable forms prior to disposal and the impact of disposing of solidified decontamination wastes. The results of the solidification of simulated decontamination resin wastes will be presented. Recent results on combustion of simulated decontamintion wastes will be described and procedures for evaluating the release of decontamination reagents from solidified wastes will be summarized

Survey of glass plutonium contents and poison selection

Energy Technology Data Exchange (ETDEWEB)

Plodinec, M.J.; Ramsey, W.G. [Westinghouse Savannah River Company, Aiken, SC (United States); Ellison, A.J.G.; Shaw, H. [Lawrence Livermore National Laboratory, CA (United States)

1996-05-01

If plutonium and other actinides are to be immobilized in glass, then achieving high concentrations in the glass is desirable. This will lead to reduced costs and more rapid immobilization. However, glasses with high actinide concentrations also bring with them undersirable characteristics, especially a greater concern about nuclear criticality, particularly in a geologic repository. The key to achieving a high concentration of actinide elements in a glass is to formulate the glass so that the solubility of actinides is high. At the same time, the glass must be formulated so that the glass also contains neutron poisons, which will prevent criticality during processing and in a geologic repository. In this paper, the solubility of actinides, particularly plutonium, in three types of glasses are discussed. Plutonium solubilities are in the 2-4 wt% range for borosilicate high-level waste (HLW) glasses of the type which will be produced in the US. This type of glass is generally melted at relatively low temperatures, ca. 1150{degrees}C. For this melting temperature, the glass can be reformulated to achieve plutonium solubilities of at least 7 wt%. This low melting temperature is desirable if one must retain volatile cesium-137 in the glass. If one is not concerned about cesium volatility, then glasses can be formulated which can contain much larger amounts of plutonium and other actinides. Plutonium concentrations of at least 15 wt% have been achieved. Thus, there is confidence that high ({ge}5 wt%) concentrations of actinides can be achieved under a variety of conditions.

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.)

Final report for the 190-D complex decontamination and decommissioning

International Nuclear Information System (INIS)

Thoren, S.D.

1996-09-01

This report documents the decontamination and decommissioning (D ampersand D) of the 190-D complex. (located on the Hanford Site in Richland, Washington). D ampersand D of the 190-D complex included decontaminating and removing hazardous and radiologically contaminated materials; dismantling equipment piping and utility infrastructure; demolishing the structure; and restoring the site. The 100-D Area contains two of the nine inactive plutonium production reactors. The reactor sites are located along the south shore of the Columbia River where the sites cover the northern part of the Hanford Site. The 190-D complex is located in the 100-D Area and is composed of the following seven buildings: 185-D De-aeration Building, 189-D Refrigeration Building, 190-D Tank Room Highbay, 190-D Process Pump Room, 190-DA Process Pump Room Annex, 195-D Vertical Safety Rod Test Tower, 1724-D Underwater Test Facility

Model decontamination of PVC flooring specimens by wet method

International Nuclear Information System (INIS)

Severa, J.; Knajfl, J.; Bar, J.

1981-01-01

PVC flooring samples of 29 mm in diameter were used in experiments. The samples were degreased. Tested were the dependence of the degree of contamination on the duration of contact with the contaminant and the efficacy of decontamination by wiping with tampons and immersing in solutions. A mixture of fission products of 80 kBq/ml in specific activity was used for contamination. Higher decontamination efficacy was achieved by immersing the samples in decontamination solutions. Water was found to be the least efficacious medium; a high degree was only attained in the case when decontamination was effected within 1 minute after contamination. The highest decontamination values were achieved using solutions containing a chelating agent and a surfactant. The most efficacious solutions contained 0.5% of citric acid and 0.5% of detergents which are very potent at a concentration as low as 2 g/l. (J.P.)

Plan for fully decontaminating and decommissioning of the Westinghouse Advanced Reactors Division Fuel Laboratories at Cheswick, Revision 3

International Nuclear Information System (INIS)

1982-01-01

The project scope of work included the complete decontamination and decommissioning (D and D) of the Westinghouse ARD Fuel Laboratories at the Cheswick Site in the shortest possible time. This has been accomplished in the following four phases: (1) preparation of documents and necessary paperwork; packaging and shipping of all special nuclear materials in an acceptable form to a reprocessing agency; (2) decontamination of all facilities, glove boxes and equipment; loading of generated waste into bins, barrels and strong wooden boxes; (3) shipping of all bins, barrels and boxes containing waste to the designated burial site; removal of all utility services from the laboratories; (4) final survey of remaining facilities and certification for nonrestricted use; preparation of final report. This volume contains the following 3 attachments: (1) Plan for Fully Decontamination and Decommissioning of the Westinghouse Advanced Reactors Division Fuel Laboratories at Cheswick; (2) Environmental Assessment for Decontamination and Decommissioning the Westinghouse Advanced Reactors Division Plutonium Fuel Laboratories, Cheswick, PA; and (3) WARD-386, Quality Assurance Program Description for Decontamination and Decommissioning Activities

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

Decontamination and materials corrosion concerns in the BWR

International Nuclear Information System (INIS)

Gordon, B.M.; Gordon, G.M.

1988-01-01

The qualification of chemical decontamination processes to decontaminate complete systems or individual components in essential if effective inspection, maintenance, repair or replacement of plant components is to be achieved with minimum exposure of workers to ionizing radiation. However, it is critical that the benefits of decontamination processes are not overshadowed by deleterious materials/ corrosion side effects during the application of the process or during subsequent operation. This paper discusses such potential corrosion/materials problems in the BWR and presents relevant available corrosion data for the various commercial decontamination processes. (author)

The use tri-n-butyl phosphate in plutonium extraction. Radiolysis and recycling of the solvent (1963); Le phosphate de tri-n-butyle dans l'extraction du plutonium. Radiolyse et recyclage du solvant (1963)

Energy Technology Data Exchange (ETDEWEB)

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

1963-07-01

The work concerns the radiolysis and recycling of tri-n-butyl phosphate used as extraction solvent for plutonium. The radiolysis is studied on an industrial solvent using a cobalt 60 source. Figures are given for the yield of the mono- and di-butyl-phosphoric acids formed from the dry and water-saturated solvents and the influence of nitric acid on the formation of dibutyl-phosphoric acid is indicated. The recycling treatment of the solvent is reconsidered with a view to lowering the residual contamination due to fission products. The tests carried out on a solvent from the plutonium extraction plant at Marcoule show the efficiency of the sodium carbonate treatment. Of all the products studied, only caustic soda led to a better decontamination than sodium carbonate; in all cases however, the elimination of ruthenium is always incomplete. (author) [French] L'etude porte sur la radiolyse et le recyclage du phosphate de tri-n-butyle utilise comme solvant d'extraction du plutonium. La radiolyse est etudiee sur un solvant industriel a l'aide d'une source de cobalt 60. On donne les rendements de formation des acides mono- et dlbutylphosphoriques a partir de solvants secs et satures d'eau, et on montre l'influence de l'acide nitrique sur la formation de l'acide dibutylphosphorique. Le traitement de recyclage du solvant est repris en vue d'abaisser la contamination residuelle en produits de fission. Les essais, effectues sur un solvant provenant de l'usine d'extraction du plutonium de Marcoule, montrent l'efficacite du traitement au carbonate de sodium. De tous les reactifs etudies, seule la soude a donne une decontamination superieure au carbonate de sodium; mais dans tous les cas, l'elimination du ruthenium est toujours incomplete. (auteur)

Alpha Decontamination and Disassembly Pilot Facility. Final report

International Nuclear Information System (INIS)

Daugherty, B.A.; Clark, H.E.

1985-04-01

The Alpha Decontamination and Disassembly (AD and D) Pilot Facility was built to develop and demonstrate a reference process for the decontamination and size reduction of noncombustible transuranic (TRU) waste. The goals of the reference process were to remove >99% of the surface contamination to the high-level waste tanks, and to achieve volume reduction factors greater than 15:1. Preliminary bench-scale decontamination work was accomplished at Savannah River Laboratory (SRL), establishing a reference decontamination process. Initially, the pilot facility did not achieve the decontamination goals. As the program continued, and modifications to the process were made, coupon analysis idicated that 99% of the surface contamination was removed to the high-level drain system. Prior to the AD and D Pilot Facility, no size reduction work had been done at SRL. Several other Department of Energy (DOE) facilities were experimenting with plasma arc torches for size reduction work. Their methods were employed in the AD and D hot cell with moderate success. The experimental work concluded with recommendations for further testing of other size reduction techniques. 11 figs., 6 tabs

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

Safety analysis for the 233-S decontamination and decommissioning project

International Nuclear Information System (INIS)

Thoren, S.

1996-08-01

Decommissioning of the 233-S Plutonium Concentration Facility (REDOX) is a proposed expedited response action that is regulated by the Comprehensive Environmental Response Compensation and Liability Act of 1980 and the Hanford Federal Facility Agreement and Consent Order. Due to progressive physical deterioration of this facility, a decontamination and decommissioning plan is being considered for the immediate future. This safety analysis describes the proposed actions involved in this D ampersand D effort; identifies the radioactive material inventories involved; reviews site specific environmental characteristics and postulates an accident scenario that is evaluated to identify resultant effects

309 plutonium recycle test reactor ion exchanger vault deactivitation report

International Nuclear Information System (INIS)

Griffin, P.W.

1996-03-01

This report documents the deactivation of the ion exchanger vault at the 309 Plutonium Recycle Test Reactor (PRTR) Facility in the 300 Area. The vault deactivation began in May 1995 and was completed in June 1995. The final site restoration and shipment of the low-level waste for disposal was finished in September 1995. The ion exchanger vault deactivation project involved the removal and disposal of twelve ion exchangers and decontaminating and fixing of residual smearable contamination on the ion exchanger vault concrete surfaces

Experience with thermal recycle of plutonium and uranium

International Nuclear Information System (INIS)

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

1985-01-01

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

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.

Treatability Studies Used to Test for Exothermic Reactions of Plutonium Decontamination Chemicals

Energy Technology Data Exchange (ETDEWEB)

Ewalt, John R.; Minette, Michael J.; Hopkins, Andrea M.; Cooper, Thurman D.; Simiele, Connie J.; Scott, Paul A.; Scheele, Randall D.; Charboneau, Stacy L.

2005-08-07

Fluor Hanford is decommissioning the PFP at the Hanford Site and is considering using agressive chemicals to remove transuranium contaminants. As part of the evaluation of these methods, Fluor is considering the path for disposal and the thermal stability of the waste products from the decontamination process. This paper provides the results of our studies on cerium nitrate and RadPro(TM), a nitric acid based complexant.

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

GrayQb^TM Single-Faced Version 2 (SF2) Hanford Plutonium Reclamation Facility (PRF) deployment report

Energy Technology Data Exchange (ETDEWEB)

Plummer, J. R. [Savannah River Site (SRS), Aiken, SC (United States); Immel, D. M. [Savannah River Site (SRS), Aiken, SC (United States); Serrato, M. G. [Savannah River Site (SRS), Aiken, SC (United States); Dalmaso, M. J. [Savannah River Site (SRS), Aiken, SC (United States); Shull, D. J. [Savannah River Site (SRS), Aiken, SC (United States)

2015-11-18

The Savannah River National Laboratory (SRNL) in partnership with CH2M Plateau Remediation Company (CHPRC) deployed the GrayQb^TM SF2 radiation imaging device at the Hanford Plutonium Reclamation Facility (PRF) to assist in the radiological characterization of the canyon. The deployment goal was to locate radiological contamination hot spots in the PRF canyon, where pencil tanks were removed and decontamination/debris removal operations are on-going, to support the CHPRC facility decontamination and decommissioning (D&D) effort. The PRF canyon D&D effort supports completion of the CHPRC Plutonium Finishing Plant Decommissioning Project. The GrayQb^TM SF2 (Single Faced Version 2) is a non-destructive examination device developed by SRNL to generate radiation contour maps showing source locations and relative radiological levels present in the area under examination. The Hanford PRF GrayQbTM Deployment was sponsored by CH2M Plateau Remediation Company (CHPRC) through the DOE Richland Operations Office, Inter-Entity Work Order (IEWO), DOE-RL IEWO- M0SR900210.

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.

An advanced purex process based on salt-free reductants

Energy Technology Data Exchange (ETDEWEB)

He, Hui; Ye, Guoan; Tang, Hongbin; Zheng, Weifang; Li, Gaoliang; Lin, Rushan [China Institute of Atomic Energy, Beijing (China). Dept. of Radiochemistry

2014-04-01

An advanced plutonium and uranium recovery process has been established based on two organic reductants, N,N-dimethylhydroxylamine (DMHAN) and methylhydrazine (MH), as U/Pu separation reagents. This Advanced Purex process based on Organic Reductants (APOR) is composed of three cycles, including U/Pu co-decontamination/separation cycle, uranium purification cycle and plutonium purification cycle. Using DMHAN and MH as plutonium stripping reagents in the U/Pu co-decontamination/separation cycle and plutonium purification cycle, the APOR process exhibits high performance with following highlights: (1) the process is much simpler because of the elimination of Tc scrubbing operation and the supplement extraction operation, (2) high efficiency of U/Pu separation can be achieved in the first cycle, (3) plutonium product solution of high concentration can be obtained in the Pu purification cycle with a simple extraction operation instead of circumfluent extraction or evaporation of the plutonium solution. (orig.)

Plasma decontamination of uranium oxide from stainless steel surfaces

International Nuclear Information System (INIS)

Veilleux, J.M.; El-Genk, M.S.; Chamberlin, E.P.

1997-01-01

The U.S. Department of Energy (DOE) is expected to have 845000 m 3 of transuranic (TRU) waste by the year 2000 that has accumulated during the development and assembly of the nation's nuclear stockpile. The TRU disposal costs alone range up to $28000/m 3 , which could be reduced to $1800/m 3 or less by treating and converting the material to low-level waste. Plasma-based processes have been shown to remove plutonium and uranium surface contaminants from metallic components and could be used to treat TRU with significant cost avoidance, estimated at over $1.0 billion. Martz and Hess conducted the initial work of plutonium etching in low-power radio-frequency (rf) plasma with etch rates ranging from 0.007 to 0.025 kg/m 2 ·h. Veilleux et al. reported that plasma decontamination of uranium from the interior of aluminum objects results in etch rates an order of magnitude greater. The current work reports on removal rates of uranium from stainless steel surfaces and includes estimates of the etch rates and characteristic times for removal

Electropolishing as a decontamination process: progress and applications

International Nuclear Information System (INIS)

Allen, R.P.; Arrowsmith, H.W.; Charlot, L.A.; Hooper, J.L.

1978-04-01

Research studies demonstrated the ability of electropolishing to reduce the radiation levels of steel tools and stainless steel vacuum system components, which were heavily contaminated with plutonium oxide, from 1 million dis/min x 100 cm 2 to background in less than 10 min. Other examples of objects that have been decontaminated within minutes using electropolishing include hot cell manipulator assemblies, analytical instrument components, laboratory transfer containers, offsite shipping containers, fission product storage capsules, laboratory animal cages, and nuclear reactor process tube components. One of the major activities of this research has been the establishment and intensive operation of a 400-gal immersion electropolishing system. Progress has also been made in developing in situ electropolishing techniques that can be used to decontaminate metallic surfaces that cannot readily be transported to or immersed in a conventional electropolishing tank. Sectioning/pretreatment studies are under way to develop and demonstrate optimum disassembly, sectioning, surface preparation, and gross contamination removal procedures. Arc saw, plasma arc torch, and explosive cutting techniques are being evaluated in terms of the thickness and characteristics of the disturbed metal layer. Some of the pretreatment methods under consideration for removal of paint, grease, corrosion layers, and gross contamination include vibratory finishing, ultrasonics, dry and liquid abrasive blasting, and high-pressure spray systems. Other supporting studies are also in progress to provide a sound technical basis for scale-up and widespread application of this new decontamination process. 44 figures

Decontamination of some liquid wastes of medium activity with a new solvent type

International Nuclear Information System (INIS)

Gasparini, G.

1986-01-01

The decontamination of a reference MAWsub(s) (an alkaline solution coming from the solvent washing and an acidic solution consisting of the mixture of aqueous raffinates deriving from uranium and plutonium purification cycles) by hydroxamic acid is reported. The results of the ''in batch'' decontamination tests, using extraction chromatography techniques, are given. The extraction chromatography techniques do not give the expected performances for the tests in column. Discontinuous liquid extraction tests using traced solutions show that Pu, Am, Zr, Nb are extracted but not U and Ru. The strip of Pu, Am and Zr with an oxalic acid solution is quantitative. Continuous tests using mixer settler batteries, and a simulated alkaline solution and complete extraction-reextraction runs using a simulated solution are conducted. The results of a discontinuous conclusive experiments using a true alkaline solution coming from a reprocessing plant are given

Decontamination of process equipment using recyclable chelating solvent

International Nuclear Information System (INIS)

Jevec, J.; Lenore, C.; Ulbricht, S.

1995-01-01

The Department of Energy (DOE) is now faced with the task of meeting decontamination and decommissioning obligations at numerous facilities by the year 2019. Due to the tremendous volume of material involved, innovative decontamination technologies are being sought that can reduce the volumes of contaminated waste materials and secondary wastes requiring disposal. With sufficient decontamination, some of the material from DOE facilities could be released as scrap into the commercial sector for recycle, thereby reducing the volume of radioactive waste requiring disposal. Although recycling may initially prove to be more costly than current disposal practices, rapidly increasing disposal costs are expected to make recycling more and more cost effective. Additionally, recycling is now perceived as the ethical choice in a world where the consequences of replacing resources and throwing away reusable materials are impacting the well-being of the environment. Current approaches to the decontamination of metals most often involve one of four basic process types: (1) chemical, (2) manual and mechanical, (3) electrochemical, and (4) ultrasonic. open-quotes Hardclose quotes chemical decontamination solutions, capable of achieving decontamination factors (Df's) of 50 to 100, generally involve reagent concentrations in excess of 5%, tend to physically degrade the surface treated, and generate relatively large volumes of secondary waste. open-quotes Softclose quotes chemical decontamination solutions, capable of achieving Df's of 5 to 10, normally consist of reagents at concentrations of 0.1 to 1%, generally leave treated surfaces in a usable condition, and generate relatively low secondary waste volumes. Under contract to the Department of Energy, the Babcock ampersand Wilcox Company is developing a chemical decontamination process using chelating agents to remove uranium compounds and other actinide species from process equipment

Radioactive decontamination

International Nuclear Information System (INIS)

1983-07-01

This Code of Practice covers: (a) the decontamination of plant items, buildings and associated equipment; (b) decontamination of protective clothing; (c) simple personal decontamination; and (d) the basic mechanisms of contamination and their influence on decontaminability. (author)

Fiscal year 1996 decontamination and decommissioning activities photobriefing book for the Argonne National Laboratory-East Site, Technology Development Division, Waste Management Program, Decontamination and Decommissioning Projects Department

International Nuclear Information System (INIS)

1996-01-01

The Photobriefing Book describes the Decontamination and Decommissioning (D and D) Program at the Argonne National Laboratory-East Site (ANL-E) near Lemont, Illinois. This book summarizes current D and D projects, reviews fiscal year (FY) 1996 accomplishments, and outlines FY 1997 goals. A section on D and D Technology Development provides insight on new technologies for D and D developed or demonstrated at ANL-E. Past projects are recapped and upcoming projects are described as Argonne works to accomplish its commitment to, ''Close the Circle on the Splitting of the Atom.'' Finally, a comprehensive review of the status and goals of the D and D Program is provided to give a snap-shot view of the program and the direction it's taking as it moves into FY 1997. The D and D projects completed to date include: Plutonium Fuel Fabrication Facility; East Area Surplus Facilities; Experimental Boiling Water Reactor; M-Wing Hot Cell Facilities; Plutonium Gloveboxes; and Fast Neutron Generator

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

Chemical decontamination for decommissioning purposes. (Vigorous decontamination tests of steel samples in a special test loop)

International Nuclear Information System (INIS)

Bregani, F.; Pascali, R.; Rizzi, R.

1984-01-01

The aim of the research activities described was to develop vigorous decontamination techniques for decommissioning purposes, taking into account the cost of treatment of the radwaste, to achieve possibly unrestricted release of the treated components, and to obtain know-how for in situ hard decontamination. The decontamination procedures for strong decontamination have been optimized in static and dynamic tests (DECO-loop). The best values have been found for: (i) hydrochloric acid: 4 to 5% vol. at low temperature, 0.7 to 1% vol. at high temperature (80 0 C); (ii) hydrofluoric plus nitric acid: 1.5% vol. HF + 5% vol. HNO 3 at low temperature; 0.3 to 0.5% vol. HF + 2.5 to 5% vol. HNO 3 at high temperature. High flow rates are not necessary, but a good re-circulation of the solution is needed. The final contamination levels, after total oxide removal, are in accordance with limits indicated for unrestricted release of materials in some countries. The arising of the secondary waste is estimated. Decontamination of a 10 m 2 surface would typically produce 0.5 to 3.0 kg of dry waste, corresponding to 1.6 to 10 kg of concrete conditioned waste

Rapid isolation of plutonium in environmental solid samples using sequential injection anion exchange chromatography followed by detection with inductively coupled plasma mass spectrometry

DEFF Research Database (Denmark)

Qiao, Jixin; Hou, Xiaolin; Roos, Per

2011-01-01

size effect upon the separation efficiency revealed that small-sized (2 mL) columns sufficed to handle up to 50 g of environmental soil samples. Under the optimum conditions, chemical yields of plutonium exceeded 90% and the decontamination factors for uranium, thorium and lead ranged from 103 to 104....... The determination of plutonium isotopes in three standard/certified reference materials (IAEA-375 soil, IAEA-135 sediment and NIST-4359 seaweed) and two reference samples (Irish Sea sediment and Danish soil) revealed a good agreement with reference/certified values. The SI column-separation method...

Weapons-grade plutonium dispositioning. Volume 1: Executive summary

International Nuclear Information System (INIS)

Parks, D.L.; Sauerbrun, T.J.

1993-06-01

The Secretary of Energy requested the National Academy of Sciences (NAS) Committee on International Security and Arms Control to evaluate dispositioning options for weapons-grade plutonium. The Idaho National Engineering Laboratory (INEL) assisted NAS in this evaluation by investigating the technical aspects of the dispositioning options and their capability for achieving plutonium annihilation levels greater than 90%. Additionally, the INEL investigated the feasibility of using plutonium fuels (without uranium) for disposal in existing light water reactors and provided a preconceptual analysis for a reactor specifically designed for destruction of weapons-grade plutonium. This four-volume report was prepared for NAS to document the findings of these studies. Volume 2 evaluates 12 plutonium dispositioning options. Volume 3 considers a concept for a low-temperature, low-pressure, low-power-density, low-coolant-flow-rate light water reactor that quickly destroys plutonium without using uranium or thorium. This reactor concept does not produce electricity and has no other mission than the destruction of plutonium. Volume 4 addresses neutronic performance, fabrication technology, and fuel performance and compatibility issues for zirconium-plutonium oxide fuels and aluminum-plutonium metallic fuels. This volumes gives summaries of Volumes 2--4

Upgrading a 1944 plutonium-extraction plant to a modern decontamination facility

International Nuclear Information System (INIS)

Wills, C.E.; Millikin, R.M.; Cruz, E.A.

1993-10-01

The Hanford Site, located in south-central Washington State, is currently undergoing extensive modifications as its mission changes from defense material production to one of waste management and environmental restoration. Starting in World War II, Hanford's mission for over four decades was the production of plutonium for defense needs. With the removal of such defense requirements over the last several years, the Hanford Site has refocused its efforts on the issues of cleanup and safety. The T Plant Complex is the first of the existing facilities to begin conversion from the old mission to the new. This conversion process and associated problems are described

ZPR-9 airborne plutonium monitoring system

International Nuclear Information System (INIS)

Rusch, G.K.; McDowell, W.P.; Knapp, W.G.

1975-01-01

An airborne plutonium monitoring system which is installed in the ZPR-9 (Zero Power Reactor No. 9) facility at Argonne National Laboratory is described. The design and operational experience are discussed. This monitoring system utilizes particle size and density discrimination, alpha particle energy discrimination, and a background-subtraction techique operating in cascade to separate airborne-plutonium activity from other, naturally occurring, airborne activity. Relatively high sensitivity and reliability are achieved

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.

OPEN AIR DEMOLITION OF FACILITIES HIGHLY CONTAMINATED WITH PLUTONIUM

International Nuclear Information System (INIS)

LLOYD, E.R.

2007-01-01

The demolition of highly contaminated plutonium buildings usually is a long and expensive process that involves decontaminating the building to near free- release standards and then using conventional methods to remove the structure. It doesn't, however, have to be that way. Fluor has torn down buildings highly contaminated with plutonium without excessive decontamination. By removing the select source term and fixing the remaining contamination on the walls, ceilings, floors, and equipment surfaces; open-air demolition is not only feasible, but it can be done cheaper, better (safer), and faster. Open-air demolition techniques were used to demolish two highly contaminated buildings to slab-on-grade. These facilities on the Department of Energy's Hanford Site were located in, or very near, compounds of operating nuclear facilities that housed hundreds of people working on a daily basis. To keep the facilities operating and the personnel safe, the projects had to be creative in demolishing the structures. Several key techniques were used to control contamination and keep it within the confines of the demolition area: spraying fixatives before demolition; applying fixative and misting with a fine spray of water as the buildings were being taken down; and demolishing the buildings in a controlled and methodical manner. In addition, detailed air-dispersion modeling was done to establish necessary building and meteorological conditions and to confirm the adequacy of the proposed methods. Both demolition projects were accomplished without any spread of contamination outside the modest buffer areas established for contamination control. Furthermore, personnel exposure to radiological and physical hazards was significantly reduced by using heavy equipment rather than ''hands on'' techniques

Depressurized pipes decontamination by using circulation foam

International Nuclear Information System (INIS)

Damerval, Frederique; Belz, Jacques; Renouf, Marjorie; Janneau, Patrice

2012-09-01

Decontamination of pipes remains a necessity in order to reduce the radiation level during maintenance or dismantling operations but it is not so easy to do it, especially in case of a long pipe network. To achieve this operation, the use of chemistry is one of the more relevant methods; moreover, the liquid waste production still remains an issue that it can be avoided by the use of decontamination foams. (authors)

Expected behavior of plutonium in the IFR fuel cycle

International Nuclear Information System (INIS)

Steunenberg, R.K.; Johnson, I.

1985-01-01

The Integral Fast Reactor (IFR) is a metal-fueled, sodium-cooled reactor that will consist initially of a U-Zr alloy core in which the enriched uranium will be replaced gradually by plutonium bred in a uranium blanket. The plutonium is concentrated to the required level by extraction from the molten blanket material with a CaCl 2 -BaCl 2 salt containing MgCl 2 as an oxidant (halide slagging). The CaCl 2 -BaCl 2 salt containing dissolved PuCl 3 and UCl 3 is added to the core process where fission products are removed by electrorefining, using a liquid cadmium anode, a metal cathode, and a LiCl-NaCl-CaCl 2 -BaCl 2 molten salt electrolyte. The product is recovered as a metallic deposit on the cathode. The halide slagging step is operated at about 1250 0 and the electrorefining step at about 450 0 C. These processes are expected to give low fission-product decontamination factors of the order of 100

Study of Thorium Phosphate Diphosphate (TPD) formation in nitric medium for the decontamination of high activity actinides bearing effluents

International Nuclear Information System (INIS)

Rousselle, Jerome

2004-01-01

Considering several activities in the nuclear industry and research, several low-level liquids wastes (LLLW) containing actinides in nitric medium must be decontaminated before being released in the environment. These liquid wastes mainly contain significant amounts of uranium(VI), neptunium(V) and plutonium(IV). In this work, two chemical ways were studied to decontaminate LLLW then to incorporate simultaneously uranium, neptunium and plutonium in the Thorium Phosphate Diphosphate (TPD). Both ways started from a nitric solution containing thorium and the actinides considered, present at their lower stable oxidation state. The first way consisted in the initial precipitation of actinide and thorium mixed oxalate. After drying the mixture containing the powder and phosphoric acid under dried argon, a poly-phase system was obtained. It was mainly composed by a thorium-actinide oxalate-phosphate. This mixture was transformed into a TPDAn solid solution (An = U, Np and/or Pu) by heating treatment at 1200 deg. C under inert atmosphere. The second way consisted in the precipitation of a precursor of TPD, identified as the Thorium Phosphate Hydrogen Phosphate loaded with the actinides considered. The gel initially formed by mixing concentrated phosphoric acid solution with the nitric actinide solution was heated at 90 - 160 deg. C in a closed PTFE container for several weeks. It led to the TPDAn solid solutions after heating at 1100 deg. C in air or under inert argon. The efficiency of both processes was evaluated through the determination of the decontamination for each actinide considered. Considering the encouraging results obtained for both kinds of processes, some complementary studies are now required before performing the effective decontamination of real Low-Level Liquid Waste using one of the methods proposed. (author) [fr

Determination and behaviour of plutonium emitted with liquid effluents and exhaust air into the environment of the Nuclear Research Centre Karlsruhe

International Nuclear Information System (INIS)

Schuettelkopf, H.; Pimpl, M.

1986-01-01

The plutonium concentrations in the surroundings of the Karlsruhe Nuclear Research Centre (KfK) are in the range of variation of the global plutonium contamination caused by fallout of atmospheric nuclear tests. Exclusively in the sediments of the Old River Rhine, which serves as main canal for the liquid effluents, higher plutonium concentrations could be detected. The dose exposure of the population living in the environment of the KfK caused by the measured plutonium concentrations is negligible low. From the Karlsruhe Reprocessing Plant (WAK) and the facilities needed to decontaminate radioactive wastes 0.48 GBq (13 mCi) plutonium alpha activity has been emitted within 11 years of operation until 1982 - 1/3 with the liquid effluents and 2/3 with the exhaust air. Following the pathway with the exhaust air, plutonium concentrations in the environment of the Karlsruhe Reprocessing Plant were measured in groundlevel air, in soil, in plants, in food and in animal tissues. Radioecological parameters like dispersion factors, deposition velocities, migration velocities in soil and transfer soil-to-plant were investigated. Following the pathway with the liquid effluents, plutonium concentrations were measured in surface waters, sediments, water plants, plankton and animals. Dilution and sedimentation behaviour were studied as well as the transfer water-to-plant and water-to-animals. (orig.) [de

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.

ANL-W MOX fuel lead assemblies data report for the surplus plutonium disposition environmental impact statement

International Nuclear Information System (INIS)

O'Connor, D.G.; Fisher, S.E.; Holdaway, R.

1997-08-01

The purpose of this document is to support the US Department of Energy (DOE) Fissile Materials Disposition Program's preparation of the draft surplus plutonium disposition environmental impact statement (EIS). This is one of several responses to data call requests for background information on activities associated with the operation of the lead assembly (LA) mixed-oxide (MOX) fuel fabrication facility. The DOE Office of fissile Materials Disposition (DOE-MD) has developed a dual-path strategy for disposition of surplus weapons-grade plutonium. One of the paths is to disposition surplus plutonium through irradiation of MOX fuel in commercial nuclear reactors. MOX fuel consists of plutonium and uranium oxides (PuO 2 and UO 2 ), typically containing 95% or more UO 2 . DOE-MD requested that the DOE Site Operations Offices nominate DOE sites that meet established minimum requirements that could produce MOX LAs. The paper describes the following: Site map and the LA facility; process descriptions; resource needs; employment requirements; wastes, emissions, and exposures; accident analysis; transportation; qualitative decontamination and decommissioning; post-irradiation examination; LA fuel bundle fabrication; LA EIS data report assumptions; and LA EIS data report supplement

ANL-W MOX fuel lead assemblies data report for the surplus plutonium disposition environmental impact statement

Energy Technology Data Exchange (ETDEWEB)

O`Connor, D.G.; Fisher, S.E.; Holdaway, R. [and others

1997-08-01

The purpose of this document is to support the US Department of Energy (DOE) Fissile Materials Disposition Program`s preparation of the draft surplus plutonium disposition environmental impact statement (EIS). This is one of several responses to data call requests for background information on activities associated with the operation of the lead assembly (LA) mixed-oxide (MOX) fuel fabrication facility. The DOE Office of fissile Materials Disposition (DOE-MD) has developed a dual-path strategy for disposition of surplus weapons-grade plutonium. One of the paths is to disposition surplus plutonium through irradiation of MOX fuel in commercial nuclear reactors. MOX fuel consists of plutonium and uranium oxides (PuO{sub 2} and UO{sub 2}), typically containing 95% or more UO{sub 2}. DOE-MD requested that the DOE Site Operations Offices nominate DOE sites that meet established minimum requirements that could produce MOX LAs. The paper describes the following: Site map and the LA facility; process descriptions; resource needs; employment requirements; wastes, emissions, and exposures; accident analysis; transportation; qualitative decontamination and decommissioning; post-irradiation examination; LA fuel bundle fabrication; LA EIS data report assumptions; and LA EIS data report supplement.

Effect of Cerium(IV)-Surfactant Reaction in Foam Decontamination

Energy Technology Data Exchange (ETDEWEB)

Yang, Han Beom; Jung, Chong-Hun; Yoon, In-Ho; Kim, Chorong; Choi, Wang-Kyu [Korea Atomic Energy Research Institute, Daejeon (Korea, Republic of)

2015-05-15

Using foams allows the decommissioning of complex shaped facilities. The decontamination foam comprises at least one surfactant to generate the foam and one or more chemical reactants to achieve the dissolution of the contaminants at the solid surface. In order to improve the efficiency of decontamination foam, the present study attempts to find the optimum condition of chemical reagents to the foaming solution. The corrosion rate of radioactive nuclides contaminated stainless steel metal is very important factor for the foam decontamination process. The goal of this study is to develop the decontamination process for contaminated stainless steel in medium of nitric acid. Stainless steel needs a strong oxidizing agent such as Ce(IV) ion and the effects of cerium(IV). Surfactant interaction involved in foam decontamination and finally the improvement brought by formulation science. The formulation of foams loaded with strong oxidizing reagents such as Ce(IV) is an important factor. The enhanced decontamination properties of nitric acid with Ce(IV) additive on stainless steel is well known in liquid mediums. stainless steel metal is an important aspect in the foam decontamination process.

Effect of Cerium(IV)-Surfactant Reaction in Foam Decontamination

International Nuclear Information System (INIS)

Yang, Han Beom; Jung, Chong-Hun; Yoon, In-Ho; Kim, Chorong; Choi, Wang-Kyu

2015-01-01

Using foams allows the decommissioning of complex shaped facilities. The decontamination foam comprises at least one surfactant to generate the foam and one or more chemical reactants to achieve the dissolution of the contaminants at the solid surface. In order to improve the efficiency of decontamination foam, the present study attempts to find the optimum condition of chemical reagents to the foaming solution. The corrosion rate of radioactive nuclides contaminated stainless steel metal is very important factor for the foam decontamination process. The goal of this study is to develop the decontamination process for contaminated stainless steel in medium of nitric acid. Stainless steel needs a strong oxidizing agent such as Ce(IV) ion and the effects of cerium(IV). Surfactant interaction involved in foam decontamination and finally the improvement brought by formulation science. The formulation of foams loaded with strong oxidizing reagents such as Ce(IV) is an important factor. The enhanced decontamination properties of nitric acid with Ce(IV) additive on stainless steel is well known in liquid mediums. stainless steel metal is an important aspect in the foam decontamination process

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

Determination of plutonium isotopes (238Pu, 239Pu, 240Pu, 241Pu) in environmental samples using radiochemical separation combined with radiometric and mass spectrometric measurements.

Science.gov (United States)

Xu, Yihong; Qiao, Jixin; Hou, Xiaolin; Pan, Shaoming; Roos, Per

2014-02-01

This paper reports an analytical method for the determination of plutonium isotopes ((238)Pu, (239)Pu, (240)Pu, (241)Pu) in environmental samples using anion exchange chromatography in combination with extraction chromatography for chemical separation of Pu. Both radiometric methods (liquid scintillation counting and alpha spectrometry) and inductively coupled plasma mass spectrometry (ICP-MS) were applied for the measurement of plutonium isotopes. The decontamination factors for uranium were significantly improved up to 7.5 × 10(5) for 20 g soil compared to the level reported in the literature, this is critical for the measurement of plutonium isotopes using mass spectrometric technique. Although the chemical yield of Pu in the entire procedure is about 55%, the analytical results of IAEA soil 6 and IAEA-367 in this work are in a good agreement with the values reported in the literature or reference values, revealing that the developed method for plutonium determination in environmental samples is reliable. The measurement results of (239+240)Pu by alpha spectrometry agreed very well with the sum of (239)Pu and (240)Pu measured by ICP-MS. ICP-MS can not only measure (239)Pu and (240)Pu separately but also (241)Pu. However, it is impossible to measure (238)Pu using ICP-MS in environmental samples even a decontamination factor as high as 10(6) for uranium was obtained by chemical separation. © 2013 Elsevier B.V. All rights reserved.

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

Actual situation on the field of decontamination in Slovak and Czech NPPs

International Nuclear Information System (INIS)

Prazska, M.; Rezbarik, J.; Solcanyi, M.; Trtilek, R.

2002-01-01

Many decontamination methods for various applications have proved to provide good results at Slovak and Czech nuclear power plants. A number of mechanical, chemical and electrochemical decontamination methods are available. The selection of a suitable method and decontamination technology is the result of a multicriterial optimization. The plants use the decontamination procedures described in the design documentation. New decontamination procedures aiming to minimize secondary radioactive wastes and corrosion attack on the basic material are being developed. No standardized qualification process, however, exists for such new procedures and large efforts are to be made to introduce them into practice. Methods for decommissioning purposes are based on static or dynamic application of decontamination solutions such as a mixture of formic acid + complexing agent + corrosion inhibitor or dilute HNO 3 . A process consisting in treatment in a solution containing formic acid + complexing agent + corrosion inhibitor (total concentration 3 - 4 mass %, temperature 30 - 35 deg C), whose effect is enhanced by the application of ultrasound (0.4 - 0.5 W per cm 2 decontaminated area) in a specially designed bath, is recommended for segmented metallic parts, which can be then released into the environment and recycled. Electrochemical decontamination in a bath is another efficient decontamination method to achieve unrestricted release of the material into the environment. Efficient decontamination of various highly contaminated materials can be attained by using an electrolyte solution based on citric acid (100 g.dm -3 ) + nitric acid (20 g.dm -3 ) + NH 4 NO 3 (50 g.dm -3 ) and applying a current density of 100 - 200 mA.cm -2 , electrolyte temperature 25 - 50 deg C, with one decontamination cycle period not exceeding 30 minutes. The best results are obtained by electrolysis followed by mechanical treatment using ultrasound. Electrochemical decontamination using a spraying

Development of advanced mixed oxide fuels for plutonium management

International Nuclear Information System (INIS)

Eaton, S.; Beard, C.; Buksa, J.; Butt, D.; Chidester, K.; Havrilla, G.; Ramsey, K.

1997-01-01

A number of advanced Mixed Oxide (MOX) fuel forms are currently being investigated at Los Alamos National Laboratory that have the potential to be effective plutonium management tools. Evolutionary Mixed Oxide (EMOX) fuel is a slight perturbation on standard MOX fuel, but achieves greater plutonium destruction rates by employing a fractional nonfertile component. A pure nonfertile fuel is also being studied. Initial calculations show that the fuel can be utilized in existing light water reactors and tailored to address different plutonium management goals (i.e., stabilization or reduction of plutonium inventories residing in spent nuclear fuel). In parallel, experiments are being performed to determine the feasibility of fabrication of such fuels. Initial EMOX pellets have successfully been fabricated using weapons-grade plutonium. (author)

Development of advanced mixed oxide fuels for plutonium management

International Nuclear Information System (INIS)

Eaton, S.; Beard, C.; Buksa, J.; Butt, D.; Chidester, K.; Havrilla, G.; Ramsey, K.

1997-06-01

A number of advanced Mixed Oxide (MOX) fuel forms are currently being investigated at Los Alamos National Laboratory that have the potential to be effective plutonium management tools. Evolutionary Mixed Oxide (EMOX) fuel is a slight perturbation on standard MOX fuel, but achieves greater plutonium destruction rates by employing a fractional nonfertile component. A pure nonfertile fuel is also being studied. Initial calculations show that the fuel can be utilized in existing light water reactors and tailored to address different plutonium management goals (i.e., stabilization or reduction of plutonium inventories residing in spent nuclear fuel). In parallel, experiments are being performed to determine the feasibility of fabrication of such fuels. Initial EMOX pellets have successfully been fabricated using weapons-grade plutonium

Determination of plutonium isotopes (²³⁸Pu, ²³⁹Pu, ²⁴⁰Pu, ²⁴¹Pu) in environmental samples using radiochemical separation combined with radiometric and mass spectrometric measurements

DEFF Research Database (Denmark)

Xu, Yihong; Qiao, Jixin; Hou, Xiaolin

2014-01-01

counting and alpha spectrometry) and inductively coupled plasma mass spectrometry (ICP-MS) were applied for the measurement of plutonium isotopes. The decontamination factors for uranium were significantly improved up to 7.5×105 for 20 g soil compared to the level reported in the literature......, this is critical for the measurement of plutonium isotopes using mass spectrometric technique. Although the chemical yield of Pu in the entire procedure is about 55%, the analytical results of IAEA soil 6 and IAEA-367 in this work are in a good agreement with the values reported in the literature or reference......Pu. However, it is impossible to measure 238Pu using ICP-MS in environmental samples even a decontamination factor as high as 106 for uranium was obtained by chemical separation....

Pipe Decontamination Involving String-Foam Circulation

International Nuclear Information System (INIS)

Turchet, J.P.; Estienne, G.; Fournel, B.

2002-01-01

Foam applications number for nuclear decontamination purposes has recently increased. The major advantage of foam decontamination is the reduction of secondary liquid wastes volumes. Among foam applications, we focus on foam circulation in contaminated equipment. Dynamic properties of the system ensures an homogeneous and rapid effect of the foam bed-drifted chemical reagents present in the liquid phase. This paper describes a new approach of foam decontamination for pipes. It is based on an alternated air and foam injections. We called it 'string-foam circulation'. A further reduction of liquid wastes is achieved compared to continuous foam. Secondly, total pressure loss along the pipe is controlled by the total foam length in the pipe. It is thus possible to clean longer pipes keeping the pressure under atmospheric pressure value. This ensures the non dispersion of contamination. This study describes experimental results obtained with a neutral foam as well with an acid foam on a 130 m long loop. Finally, the decontamination of a 44 meters pipe is presented. (authors)

Environmental decontamination

International Nuclear Information System (INIS)

Cristy, G.A.; Jernigan, H.C.

1981-02-01

The record of the proceedings of the workshop on environmental decontamination contains twenty-seven presentations. Emphasis is placed upon soil and surface decontamination, the decommissioning of nuclear facilities, and assessments of instrumentation and equipment used in decontamination

Cost/risk/benefit analysis report on the decontamination and decommissioning of Z-plant

International Nuclear Information System (INIS)

Melvin, J.P.; Sexton, R.A.; Fort, M.L.; Nunn, S.E.

1979-01-01

This study was performed to estimate the cost of decontaminating and decommissioning Z-Plant. All of the buildings in the Z-Plant exclusion area except Building 2736-Z, the plutonium storage vault, are included in the study. The study also excludes all underground facilities within the exclusion area which are not contained within a building and all Z-Plant related facilities outside the perimeter fence. The contamination in Z-Plant is primarily 239 Pu which has a half-life of 24,360 years. Because of the long half-life of 239 Pu, it is not practical to consider the isolation of the facility to await reduction of the contamination level by natural decay. Therefore, this study analyzes the costs, risk and benefit of decontaminating Z-Plant to four different levels of residual contamination. The three principle criteria used in the analysis are cost, the risk of offsite dose to the public, and the occupational exposure to onsite personnel

Cost/risk/benefit analysis report on the decontamination and decommissioning of Z-plant

Energy Technology Data Exchange (ETDEWEB)

Melvin, J. P.; Sexton, R. A.; Fort, M. L.; Nunn, S. E.

1979-09-28

This study was performed to estimate the cost of decontaminating and decommissioning Z-Plant. All of the buildings in the Z-Plant exclusion area except Building 2736-Z, the plutonium storage vault, are included in the study. The study also excludes all underground facilities within the exclusion area which are not contained within a building and all Z-Plant related facilities outside the perimeter fence. The contamination in Z-Plant is primarily /sup 239/Pu which has a half-life of 24,360 years. Because of the long half-life of /sup 239/Pu, it is not practical to consider the isolation of the facility to await reduction of the contamination level by natural decay. Therefore, this study analyzes the costs, risk and benefit of decontaminating Z-Plant to four different levels of residual contamination. The three principle criteria used in the analysis are cost, the risk of offsite dose to the public, and the occupational exposure to onsite personnel.

Environmental decontamination

Energy Technology Data Exchange (ETDEWEB)

Cristy, G.A.; Jernigan, H.C. (eds.)

1981-02-01

The record of the proceedings of the workshop on environmental decontamination contains twenty-seven presentations. Emphasis is placed upon soil and surface decontamination, the decommissioning of nuclear facilities, and assessments of instrumentation and equipment used in decontamination. (DLS)

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)

Salt decontamination demonstration test results

International Nuclear Information System (INIS)

Snell, E.B.; Heng, C.J.

1983-06-01

The Salt Decontamination Demonstration confirmed that the precipitation process could be used for large-scale decontamination of radioactive waste sale solution. Although a number of refinements are necessary to safely process the long-term requirement of 5 million gallons of waste salt solution per year, there were no observations to suggest that any fundamentals of the process require re-evaluation. Major accomplishments were: (1) 518,000 gallons of decontaminated filtrate were produced from 427,000 gallons of waste salt solution from tank 24H. The demonstration goal was to produce a minimum of 200,000 gallons of decontaminated salt solution; (2) cesium activity in the filtrate was reduced by a factor of 43,000 below the cesium activity in the tank 24 solution. This decontamination factor (DF) exceeded the demonstration goal of a DF greater than 10,000; (3) average strontium-90 activity in the filtrate was reduced by a factor of 26 to less than 10 3 d/m/ml versus a goal of less than 10 4 d/m/ml; and (4) the concentrated precipitate was washed to a final sodium ion concentration of 0.15 M, well below the 0.225 M upper limit for DWPF feed. These accomplishments were achieved on schedule and without incident. Total radiation exposure to personnel was less than 350 mrem and resulted primarily from sampling precipitate slurry inside tank 48. 3 references, 6 figures, 2 tables

Soil decontamination with Extraksol

International Nuclear Information System (INIS)

Paquin, J.; Mourato, D.

1989-01-01

The Extraksol process is a mobile decontamination technology which treats unconsolidated materials by solvent extraction. Treatment with Extraksol involves material washing, drying and solvent regeneration. Contaminant removal is achieved through desorption/dissolution mechanisms. The treated material is dry and acceptable to be reinstalled in its original location. The process provides a fast, efficient and versatile alternative for decontamination of soil and sludge. The organic contaminants extracted from the matrix are transferred to the extraction fluids. These are thereafter concentrated in the residues of distillation after solvent regeneration. Removal and concentration of the contaminants ensures an important waste volume reduction. This paper presents the process is operational principles and the steps involved in Extraksol's development with results of the pilot tests and full-scale demonstrations

Urban Decontamination Experience at Pripyat Ukraine - 13526

Energy Technology Data Exchange (ETDEWEB)

Paskevych, Sergiy [Institute for Safety Problems of Nuclear Power Plants, National Academy of Sciences of Ukraine, 36 a Kirova str. Chornobyl, Kiev region, 07200 (Ukraine); Voropay, Dmitry [Federal State Unitary Enterprise ' Russian State Center of Inventory and Registration and Real Estate - Federal Bureau of Technical Inventory' , 37-2 Bernadsky Prospekt, Moscow Russia 119415 (Russian Federation); Schmieman, Eric [Battelle Memorial Institute, PO Box 999 MSIN K6-90, Richland, WA 99352 (United States)

2013-07-01

This paper describes the efficiency of radioactive decontamination activities of the urban landscape in the town of Pripyat, Ukraine. Different methods of treatment for various urban infrastructure and different radioactive contaminants are assessed. Long term changes in the radiation condition of decontaminated urban landscapes are evaluated: 1. Decontamination of the urban system requires the simultaneous application of multiple methods including mechanical, chemical, and biological. 2. If a large area has been contaminated, decontamination of local areas of a temporary nature. Over time, there is a repeated contamination of these sites due to wind transport from neighboring areas. 3. Involvement of earth-moving equipment and removal of top soil by industrial method achieves 20-fold reduction in the level of contamination by radioactive substances, but it leads to large amounts of waste (up to 1500 tons per hectare), and leads to the re-contamination of treated areas due to scatter when loading, transport pollutants on the wheels of vehicles, etc.. (authors)

Decontamination of radionuclides on construction materials

International Nuclear Information System (INIS)

Samuleev, P.V.; Andrews, W.S.; Creber, K.A.M.; Velicogna, D.

2013-01-01

A wide variety of materials can become contaminated by radionuclides, either from a terrorist attack or an industrial or nuclear accident. The final disposition of these materials depends, in large part, on the effectiveness of decontamination measures. This study reports on investigations into the decontamination of a selection of building materials. The aim has been to find an effective, easy-to-use and inexpensive decontamination system for radionuclides of cesium and cobalt, considering both the chemical and physical nature of these potential contaminants. The basic method investigated was surface washing, due to its ease and simplicity. In the present study, a basic decontamination formulation was modified by adding isotope-specific sequestering agents, to enhance the removal of cesium(I) and cobalt(II) from such construction materials as concrete, marble, aluminum and painted steel. Spiking solutions contained 134 Cs or 60 Co, which were prepared by neutron activation in the SLOWPOKE-2 nuclear reactor facility at the Royal Military College of Canada. Gamma spectroscopy was used to determine the decontamination efficiency. The results showed that the addition of sequestering agents generally improved the radiological decontamination. Although the washing of both cesium and cobalt from non-porous materials, such as aluminum and painted steel, achieved a 90-95 % removal, the decontamination of concrete and marble was more challenging, due to the porous nature of the materials. Nevertheless, the removal efficiency from 6-year-old concrete increased from 10 % to approximately 50 % for cobalt(II), and from 18 to 55 % for cesium(I), with the use of isotope binding agents, as opposed to a simple water wash. (author)

Volume reduction and material recirculation by freon decontamination

International Nuclear Information System (INIS)

Berners, O.; Buhmann, D.; Yamashita, Y.; Yoshiaki, M.

1989-01-01

This paper discusses the use of freon in a large variety of decontamination in the nuclear and non-nuclear fields. As far as the contamination is loose or smerable, surfaces of nearly all materials can be decontaminated. Freon is electrically non-conductive, chemically neutral and has a low surface tension. So it is capable of creeping under the contaminant and loosening or dissolving it. Used freon can be collected, cleaned and recirculated. Its cleaning can be done easily by evaporation at its lower vapor point of about 48 degrees C (104 degrees F). Good decontamination results could be achieved, expensive materials, tools and equipment could be recirculated. Big volumes of materials could get separated from their contaminants, which is the real radioactive waste. Freon decontamination is an effective, overall economical and approved technology to volume reduction and material recirculation

Chemical decontamination method

International Nuclear Information System (INIS)

Nishiwaki, Hitoshi.

1996-01-01

Metal wastes contaminated by radioactive materials are contained in a rotational decontamination vessel, and the metal wastes are rotated therein while being in contact with a slight amount of a decontamination liquid comprising a mineral acid. As the mineral acid, a mixed acid of nitric acid, hydrochloric acid and fluoric acid is preferably used. Alternatively, chemical decontamination can also be conducted by charging an acid resistant stirring medium in the rotational decontamination vessel. The surface of the metal wastes is uniformly covered by the slight amount of decontamination liquid to dissolve the surface layer. In addition, heat of dissolution generated in this case is accumulated in the inside of the rotational decontamination vessel, the temperature is elevated with no particular heating, thereby enabling to obtain an excellent decontamination effect substantially at the same level as in the case of heating the liquid to 70degC in a conventional immersion decontamination method. Further, although contact areas between the metal wastes and the immersion vessel are difficult to be decontaminated in the immersion decontamination method, all of areas can be dissolved uniformly in the present invention. (T.M.)

Calculating the plutonium in spent fuel elements

International Nuclear Information System (INIS)

Barnham, Keith

1992-01-01

Many members of the public are concerned about plutonium. They are worried about its environmental, health and proliferation risks. Fundamental to all such considerations are two related questions: how much plutonium do nuclear reactors produce ? and how accurately do the relevant authorities know these production figures ? These two questions have been studied with particular reference to the UK civil Magnox reactors. In 1990 these were still the only UK civil reactors whose spent fuel had been reprocessed to extract plutonium in routine production. It has not been possible to conclude that the relevant government industry and safeguard authorities are aware of how much plutonium these reactors produce and that the figures are known to the highest achievable accuracy. To understand why, this chapter will outline some of the history of the attempts to get answers to these two questions. (author)

Development of remote electrochemical decontamination for hot cell applications

International Nuclear Information System (INIS)

Turner, A.D.; Junkison, A.R.; Pottinger, J.S.; Lain, M.J.; Neville, M.D.; Dawson, R.K.; Fletcher, P.A.; Fenn-Tye, I.A.

1993-01-01

Electrochemical dissolution into nitric acid has been developed as a decontamination process for metallic items, both for immersion and in-situ use. Not only is the spent electrolyte compatible with existing waste treatment routes, potentially yielding an immobilized product volume of 0.6 dm 3 /m 2 area treated, but it also suppresses any hydrogen production. Both processes have been developed from laboratory to microprocessor-controlled pilot-scale units, which have been demonstrated successfully for the treatment of genuine waste, reducing activity levels to background. For stainless steel substrates, the immersion tank process uses low current densities (10-50 A/m 2 ) in 1-5M HN0 3 for the treatment of extended areas. Decontamination factors > 10 4 can be achieved in two hours. The in-situ technique uses electropolishing in 6M HN0 3 at 1-2 A/cm 2 in an engineered head. Decontamination factors > 10 3 can be achieved in only 20 seconds. This device has also shown potential for incorporation into an integrated monitoring/decontaminating system under robotic control. Both techniques may be used remotely as a way of reducing man-dose and improving productivity during decontamination. Additional cost savings can be made over currently used techniques through the decategorization of the bulk of the waste volume, and the volume reduction of waste for interim storage and geological disposal

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

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

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.)

Containers for short-term storage of nuclear materials at the Los Alamos plutonium facility

International Nuclear Information System (INIS)

Hagan, R.; Gladson, J.

1997-01-01

The Los Alamos Plutonium Facility for the past 18 yr has stored nuclear samples for archiving and in support of nuclear materials research and processing programs. In the past several years, a small number of storage containers have been found in a deteriorated condition. A failed plutonium container can cause personnel contamination exposure and expensive physical area decontamination. Containers are stored in a physically secure radiation area vault, making close inspection costly in the form of personnel radiation exposure and work time. A moderate number of these containers are used in support of plutonium processing and must withstand daily handling abuse. A 2-yr evaluation of failed containers and those that have shown no deterioration has been conducted. Based on that study, a program was established to formalize our packing methods and materials and standardize the size and shape of containers that are used for short-term use. A standardized set of containers was designed, evaluated, tested, and procured for use in the facility. This paper reviews our vault storage problems, shows some failed containers, and presents our planned solutions to provide safe and secure containment of nuclear materials

Skin decontamination

International Nuclear Information System (INIS)

Moehrle, G.

1975-01-01

A general survey of skin decontamination is given. The success of every decontamination treatments depends mainly on the speed, but also on the care, with which the action is taken. The best way to remove the skin contaminants is thorough washing under lukewarm running water with mild soap and a soft brush. This washing is to be repeated several times for a period of several minutes. If results are not satisfactory, light duty detergents and wetting agents available commercially may also be used. Some solutions which have proved useful are mentioned. The decontamination solutions are best used in the order given. When one has no satisfactory decontamination effect, the next one is to be used. If necessary, these agents must be used several times in the stated order as long as this does not involve too much strain for the skin. All the decontamination measures mentioned refer, of course, to intact healthy skin. After decontamination has been completed, the skin should be treated with a protective cream

Plutonium dissolution from Rocky Flats Plant incinerator ash

International Nuclear Information System (INIS)

Delegard, C.H.

1985-06-01

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

Decontamination of radioactively polluted game by means of pickling

International Nuclear Information System (INIS)

Hecht, H.

1987-01-01

The effect of pickling on the decontamination of game polluted by radioactive cesium isotopes has been investigated in the study reported. The best decontamination degree has been achieved with a vinegar marinade, the ratio between game and marinade being 1:3, pickling temperature being maintained at 12 0 C for a period of 4 days. By this procedure, 90 p.c. of the cesium isotopes have been taken up by the marinade. Buttermilk marinade also is a successful means of decontamination, but with clearly lower effects, and at the same temperature of 12 0 C does not remain microbiologically stable. Spices added to the marinade have shown to reduce the decontamination effet. Also, the ratio between game and marinade has been found to be decisive, the best ratio being 1:3. (orig./MG) [de

Management of Russian military plutonium

International Nuclear Information System (INIS)

Zaleski, C.P.

1996-01-01

The objective of this paper is to propose and discuss a solution which enables storing as quickly as possible all weapons-grade plutonium from Russian military program in a way which would prevent diversion. Two main conditions apply to this solution. First, it should be achieved in a manner acceptable to Russian government, notably by preserving plutonium for possible future energy production, and second, the economics of the total system should be good enough to ensure no charge or limited charge for the storage of plutonium. A proposal is made to store plutonium in a specially designed fast reactor or specially designed reactor core. This solution could be favorable in comparison to other solutions applying the above mentioned goal and conditions. Additionally the proposed solution would have the following side advantages: utilizing available personnel and installations of the Russian nuclear complex; providing possible basis for decommissioning of older and less safe Russian reactors; giving experience of construction and operation of a series of sodium-cooled fast reactors. The major problem however is the need for large capital investment with the risk of getting no adequate return on investment due to difficult political and economic situation in Russia

Decontamination

International Nuclear Information System (INIS)

Montford, B.

1975-01-01

Development of special techniques has permitted the use of mild decontamination processes for the CANDU type reactor primary coolant circuit, overcoming many of the problems associated with conventional decontamination processes, which use strong, acidic reagents. (Author)

Recovery and purification of uranium-234 from aged plutonium-238

International Nuclear Information System (INIS)

Keister, P.L.; Figgins, P.W.; Watrous, R.M.

1978-01-01

The current production methods used to recover and purify uranium-234 from aged plutonium-238 at Mound Laboratory are presented. The three chemical separation steps are described in detail. In the initial separation step, the bulk of the plutonium is precipitated as the oxalate. Successively lower levels of plutonium are achieved by anion exchange in nitrate media and by anion exchange in chloride media. The procedures used to characterize and analyze the final U 3 O 8 are given

Utilization of plutonium in HTGR and its actinide production

International Nuclear Information System (INIS)

Karin, S.; Brogli, R.; Lefler, W.; Nordheim, L.

1976-01-01

The HTGR is a potential plutonium consumer. In this function it would burn plutonium, produce electricity and the valuable fissile isotope U-233. The advantages of this concept are discussed but particular attention is given to the production and the destruction of the higher actinides due to the high burnup achievable in such a system. The presence of the strong resonances in the plutonium isotopes demanded an extension of the methods for evaluation of self-shielding factors, a different structure for broad groups, and the adaptation of the reactor codes to these changes. Specifications for coated plutonium particles were developed. Also procedures were determined to evaluate the alpha ray and neutron emission rates of the actinide nuclides. First cycle calculations were carried out to establish in detail the characteristics of the plutonium reactors and their results are given

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

Decontamination in a Russian settlement

DEFF Research Database (Denmark)

Fogh, C.L.; Andersson, Kasper Grann; Barkovsky, A.N.

1999-01-01

Decontamination was carried out in an area with three houses in Novo Bobovichi, Bryansk region, Russia, in the autumn of 1995. It was demonstrated that significant reductions in the dose rate both indoor (DRF = 0.34) and outdoor (DRF = 0.20) can be achieved when a controlled cleaning is undertake...

Separation of neptunium from uranium and plutonium in the Purex process

International Nuclear Information System (INIS)

Kolarik, Z.; Schuler, R.

1984-01-01

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

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

Decontamination of steel by melt refining: A literature review

International Nuclear Information System (INIS)

Ozturk, B.; Fruehan, R.J.

1994-01-01

It has been reported that a large amount of metal waste is produced annually by nuclear fuel processing and nuclear power plants. These metal wastes are contaminated with radioactive elements, such as uranium and plutonium. Current Department of Energy guidelines require retrievable storage of all metallic wastes containing transuranic elements above a certain level. Because of high cost, it is important to develop an effective decontamination and volume reduction method for low level contaminated metals. It has been shown by some investigators that a melt refining technique can be used for the processing of the contaminated metal wastes. In this process, contaminated metal is melted wit a suitable flux. The radioactive elements are oxidized and transferred to a slag phase. In order to develop a commercial process it is important to have information on the thermodynamics and kinetics of the removal. Therefore, a literature search was carried out to evaluate the available information on the decontamination uranium and transuranic-contaminated plain steel, copper and stainless steel by melt a refining technique. Emphasis was given to the thermodynamics and kinetics of the removal. Data published in the literature indicate that it is possible to reduce the concentration of radioactive elements to a very low level by the melt refining method. 20 refs

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

International Nuclear Information System (INIS)

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

1989-01-01

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

Decontamination and dismantling of large plutonium-contamined glove boxes

International Nuclear Information System (INIS)

Draulans, J.

1991-01-01

This report describes the work performed in the frame of two C.E.C. - Contracts FI1D-002400-B Decommissioning of very large glove boxes and FI1D-0058 Decommissioning of a complex glove box structure to be dismounted partially on place. Detailed information is given about each glove box. The selection of the solution Transportation of the glove boxes to a specialized dismantling plant is justified. The necessary contacts inside the BELGONUCLEAIRE MOX plant and between the latter and other organizations are explained. The problems of manipulating large gloves are listed and the retained solution of building a so called Stiffening frame around each glove box is described. Furthermore information is given concerning required operators time for cleaning, manipulating, packing and dismantling together with received doses and quantities of waste produced. Concerning the glove box unit partially to be dismounted on place, detailed information is given about the way the glove boxes have been treated prior to this partial dismantling on place and about the way this partial dismantling has been performed. From these results one can conclude that such a delicate task can be performed without major difficulties. Finally information is given of the decontamination test of a highly Pu contaminated glove box with freon with rather poor results and of the preliminary CO 2 blasting tests on non active samples

Agricultural soils decontamination techniques: methods and results of tests realized near Chernobyl

International Nuclear Information System (INIS)

Maubert, H.; Jouve, A.; Mary, N.

1992-01-01

After a major nuclear accident, decontamination of agricultural soils would be necessary in order to reclaim the land. Specific techniques were studied in the framework of the European program for Rehabilitation of Soils and Surfaces after an Accident (RESSAC). Different ways to remove the top layer of soils are described, and especially the use of Decontaminating Vegetal Network (D.V.N.) combined with spraying of organic polymers. Real scale tests in the 30 km zone around the Chernobyl nuclear power plant showed that it is possible to achieve an excellent decontamination of agricultural fields (decontamination factor greater than 95%. (author)

The mysterious world of plutonium metallurgy: Past and future

International Nuclear Information System (INIS)

Hecker, S.S.; Hammel, E.F.

1998-01-01

The first atomic bomb detonated at the Trinity Site in New Mexico on July 16, 1945, used plutonium, a man-made element discovered < 5 yr earlier. The story of how Manhattan Project scientists and engineers tackled the mysteries of this element and fabricated it into the first atomic bomb is one of the most fascinating in the history of metallurgy and materials. The authors are currently trying to generate renewed interest in plutonium metallurgy because of the challenge posed by President Clinton, i.e., to keep the nuclear stockpile of weapons safe and reliable without nuclear testing. The stockpile stewardship challenge requires either a lifetime extension of the plutonium components or a remanufacture--neither of which can be verified by testing. In turn, this requires that one achieve a better fundamental understanding of plutonium. Of special interest is the effect of self-irradiation on the properties and on the long-term stability of plutonium and its alloys. Additional challenges arise from long-term concerns about disposing of plutonium and dealing with its environmental legacy. It is imperative to interest the next generation of students in these plutonium challenges

Cleanup of building 3019 and surroundings at ORNL following plutonium release of November 20, 1959

International Nuclear Information System (INIS)

Parrott, J.R. Sr.

1981-01-01

A non-nuclear explosion involving an evaporator occurred in a shielded cell in the Radiochemical Processing Pilot Plant at Oak Ridge National Laboratory on November 20, 1959. Plutonium was released, probably as an aerosol of fine particles of plutonium oxide, via three principal routes: (1) cell ventilation system: collected about 1.5 g, completely removed from the air stream by roughing and absolute filters; (2) the cell door was blown open (but not off) to the outside, releasing approximately 600 mg to a limited area south and east of the building. The Graphite Reactor Building, directly east of Building 3019, was subjected to the highest level of contamination; and (3) pipe passages and service openings through the cell wall resulted in about 70 mg being spread to the building interior. The extent of contamination and the decontamination effort required for resumption of operations is discussed

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

W-12 valve pit decontamination demonstration

International Nuclear Information System (INIS)

Benson, C.E.; Parfitt, J.E.; Patton, B.D.

1995-12-01

Waste tank W-12 is a tank in the ORNL Low-Level Liquid Waste (LLLW) system that collected waste from Building 3525. Because of a leaking flange in the discharge line from W-12 to the evaporator service tank (W-22) and continual inleakage into the tank from an unknown source, W-12 was removed from service to comply with the Federal Facilities Agreement requirement. The initial response was to decontaminate the valve pit between tank W-12 and the evaporator service tank (W-22) to determine if personnel could enter the pit to attempt repair of the leaking flange. Preventing the spread of radioactive contamination from the pit to the environment and to other waste systems was of concern during the decontamination. The drain in the pit goes to the process waste system; therefore, if high-level liquid waste were generated during decontamination activities, it would have to be removed from the pit by means other than the available liquid waste connection. Remote decontamination of W-12 was conducted using the General Mills manipulator bridge and telescoping trolley and REMOTEC RM-10 manipulator. The initial objective of repairing the leaking flange was not conducted because of the repair uncertainty and the unknown tank inleakage. Rather, new piping was installed to empty the W-12 tank that would bypass the valve pit and eliminate the need to repair the flange. The radiological surveys indicated that a substantial decontamination factor was achieved

Cleanout and decontamination of radiochemical hot cells

International Nuclear Information System (INIS)

Surma, J.E.; Holton, L.K. Jr.; Katayama, Y.B.; Gose, J.E.; Haun, F.E.; Dierks, R.D.

1990-01-01

The Pacific Northwest Laboratory is developing and employing advanced remote and contact technologies in cleaning out and decontaminating six radiochemical hot cells at Hanford under the Department of Energy's Surplus Facilities Management Program. The program is using a series of remote and contact decontamination techniques to reduce costs and to significantly lower radiation doses to workers. Refurbishment of the cover blocks above the air lock trench reduced radiation exposure in the air lock and cleanout and decontamination of an analytical cell achieved a reduction in radioactive contamination. Nuclear Regulatory Commission-approved Type B burial boxes are also being used to reduce waste disposal costs and radiation doses. PNL is currently decommissioning its pilot-scale radioactive liquid-fed ceramic melter. Special tools have been developed and are being used to accomplish the world's first such effort. 4 refs., 5 figs

Transmutation of plutonium in pebble bed type high temperature reactors

International Nuclear Information System (INIS)

Bende, E.E.

1997-01-01

The pebble bed type High Temperature Reactor (HTR) has been studied as a uranium-free burner of reactor grade plutonium. In a parametric study, the plutonium loading per pebble as well as the type and size of the coated particles (CPs) have been varied to determine the plutonium consumption, the final plutonium burnup, the k ∞ and the temperature coefficients as a function of burnup. The plutonium loading per pebble is bounded between 1 and 3 gr Pu per pebble. The upper limit is imposed by the maximal allowable fast fluence for the CPs. A higher plutonium loading requires a longer irradiation time to reach a desired burnup, so that the CPs are exposed to a higher fast fluence. The lower limit is determined by the temperature coefficients, which become less negative with increasing moderator-actinide ratio. A burnup of about 600 MWd/kgHM can be reached. With the HTR's high efficiency of 40%, a plutonium supply of 1520 kg/GW e a is achieved. The discharges of plutonium and minor actinides are then 450 and 110 kg/GW e a, respectively. (author)

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

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

Planning guidance for nuclear-power-plant decontamination. [PWR; BWR

Energy Technology Data Exchange (ETDEWEB)

Munson, L.F.; Divine, J.R.; Martin, J.B.

1983-06-01

Direct and indirect costs of decontamination are considered in the benefit-cost analysis. A generic form of the benefit-cost ratio is evaluated in monetary and nonmonetary terms, and values of dollar per man-rem are cited. Federal and state agencies that may have jurisiction over various aspects of decontamination and waste disposal activities are identified. Methods of decontamination, their general effectiveness, and the advantages and disadvantages of each are outlined. Dilute or concentrated chemical solutions are usually used in-situ to dissolve the contamination layer and a thin layer of the underlying substrate. Electrochemical techniques are generally limited to components but show high decontamination effectiveness with uniform corrosion. Mechanical agents are particularly appropriate for certain out-of-system surfaces and disassembled parts. These processes are catagorized and specific concerns are discussed. The treatment, storage, and disposal or discharge or discharge of liquid, gaseous, and solid wastes generated during the decontamination process are discussed. Radioactive and other hazardous chemical wastes are considered. The monitoring, treatment, and control of radioactive and nonradioactive effluents, from both routine operations and possible accidents, are discussed. Protecting the health and safety of personnel onsite during decontamination is of prime importance and should be considered in each facet of the decontamination process. The radiation protection philosophy of reducing exposure to levels as low as reasonably achievable should be stressed. These issues are discussed.

Decontamination Efficacy and Skin Toxicity of Two Decontaminants against Bacillus anthracis.

Directory of Open Access Journals (Sweden)

Chad W Stratilo

Full Text Available Decontamination of bacterial endospores such as Bacillus anthracis has traditionally required the use of harsh or caustic chemicals. The aim of this study was to evaluate the efficacy of a chlorine dioxide decontaminant in killing Bacillus anthracis spores in solution and on a human skin simulant (porcine cadaver skin, compared to that of commonly used sodium hypochlorite or soapy water decontamination procedures. In addition, the relative toxicities of these decontaminants were compared in human skin keratinocyte primary cultures. The chlorine dioxide decontaminant was similarly effective to sodium hypochlorite in reducing spore numbers of Bacillus anthracis Ames in liquid suspension after a 10 minute exposure. After five minutes, the chlorine dioxide product was significantly more efficacious. Decontamination of isolated swine skin contaminated with Bacillus anthracis Sterne with the chlorine dioxide product resulted in no viable spores sampled. The toxicity of the chlorine dioxide decontaminant was up to two orders of magnitude less than that of sodium hypochlorite in human skin keratinocyte cultures. In summary, the chlorine dioxide based decontaminant efficiently killed Bacillus anthracis spores in liquid suspension, as well as on isolated swine skin, and was less toxic than sodium hypochlorite in cultures of human skin keratinocytes.

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.

Decontamination of nuclear facilities

International Nuclear Information System (INIS)

1982-01-01

Thirty-seven papers were presented at this conference in five sessions. Topics covered include regulation, control and consequences of decontamination; decontamination of components and facilities; chemical and non-chemical methods of decontamination; and TMI decontamination experience

Surface decontamination

International Nuclear Information System (INIS)

Silva, S. da; Teixeira, M.V.

1986-06-01

The general methods of surface decontamination used in laboratory and others nuclear installations areas, as well as the procedures for handling radioactive materials and surfaces of work are presented. Some methods for decontamination of body external parts are mentioned. The medical supervision and assistance are required for internal or external contamination involving or not lesion in persons. From this medical radiation protection decontamination procedures are determined. (M.C.K.) [pt

Reactive decontamination formulation

Science.gov (United States)

Giletto, Anthony [College Station, TX; White, William [College Station, TX; Cisar, Alan J [Cypress, TX; Hitchens, G Duncan [Bryan, TX; Fyffe, James [Bryan, TX

2003-05-27

The present invention provides a universal decontamination formulation and method for detoxifying chemical warfare agents (CWA's) and biological warfare agents (BWA's) without producing any toxic by-products, as well as, decontaminating surfaces that have come into contact with these agents. The formulation includes a sorbent material or gel, a peroxide source, a peroxide activator, and a compound containing a mixture of KHSO.sub.5, KHSO.sub.4 and K.sub.2 SO.sub.4. The formulation is self-decontaminating and once dried can easily be wiped from the surface being decontaminated. A method for decontaminating a surface exposed to chemical or biological agents is also disclosed.

Chemical decontamination and melt densification of chop-leach fuel hulls

International Nuclear Information System (INIS)

Dillon, R.L.; Griggs, B.; Kemper, R.S.; Nelson, R.G.

1976-01-01

This paper reports on decontamination and densification studies of chop-leach fuel hull residues designed to minimize the transuranic element (TRU) contaminated waste stream. Decontamination requirements have been established from studies of TRU element distribution in the fuel hull residues. Effective surface decontamination of Zircaloy requires removal of zirconium oxide corrosion products. Good decontamination factors have been achieved with aqueous solutions following high temperature HF conditioning of oxide films. Molten fluoride salt mixtures are effective decontaminants, but pose problems in metal loss and salt dragout. Molten metal decontamination methods are highly preliminary, but may be required to reduce TRU originating from tramp uranium in Zircaloy. Low melting (1300 0 C) alloy of Zircaloy, stainless steel, and Inconel have been prepared in induction heated graphite crucibles. High quality ingots of Zircaloy-2 have been prepared directly from short sections of descaled fuel clad tubing using the Inductoslag process. This material is readily capable of refabrication. Inductoslag melts have also been prepared from heavily oxidized Zircaloy tubing demonstrating melt densification without prior decontamination is technically feasible. Hydrogen absorption kinetics have been demonstrated with cast Zircaloy-2 and cast Zircaloy-stainless steel-Inconel alloys. Metallic fuel hull residues have been proposed as a storage medium for tritium released from fuel during reprocessing. (author)

Development of decontamination system for radioactive matter on paved road using dry ice blast method

International Nuclear Information System (INIS)

Nagamine, Haruo; Wakayama, Masanori; Nakamura, Hiroshi

2014-01-01

As a decontamination method for paved road surface, the 'Dry Ice Blast Decontamination System' has been developed. This decontamination system has characteristic as follows; 1) Generation of decontamination waste is extremely small, 2) not using water, 3) not damaging the pavement surface. In actual decontamination work, more than 60% average (maximum 84%) reduction rate of the radiation counting rate has been achieved. In addition to these features, this system prevent the diffusion into the surrounding and the radiation exposure of workers by sucking waste quickly using attached dust collecting function. This system is also characterized in that it does not cause a difference in skill by the operator because of faceted decontamination using repetitive motion by concatenating three pellet injection nozzle and self-propelled decontamination machine. (author)

Plutonium Disposition by Immobilization

International Nuclear Information System (INIS)

Gould, T.; DiSabatino, A.; Mitchell, M.

2000-01-01

The ultimate goal of the Department of Energy (DOE) Immobilization Project is to develop, construct, and operate facilities that will immobilize between 17 to 50 tonnes (MT) of U.S. surplus weapons-usable plutonium materials in waste forms that meet the ''spent fuel'' standard and are acceptable for disposal in a geologic repository. Using the ceramic can-in-canister technology selected for immobilization, surplus plutonium materials will be chemically combined into ceramic forms which will be encapsulated within large canisters of high level waste (HLW) glass. Deployment of the immobilization capability should occur by 2008 and be completed within 10 years. In support of this goal, the DOE Office of Fissile Materials Disposition (MD) is conducting development and testing (D and T) activities at four DOE laboratories under the technical leadership of Lawrence Livermore National Laboratory (LLNL). The Savannah River Site has been selected as the site for the planned Plutonium Immobilization Plant (PIP). The D and T effort, now in its third year, will establish the technical bases for the design, construction, and operation of the U. S. capability to immobilize surplus plutonium in a suitable and cost-effective manner. Based on the D and T effort and on the development of a conceptual design of the PIP, automation is expected to play a key role in the design and operation of the Immobilization Plant. Automation and remote handling are needed to achieve required dose reduction and to enhance operational efficiency

Decontamination of CAGR gas circulator components

International Nuclear Information System (INIS)

Rogers, L.N.; Hooper, A.J.

1985-01-01

This paper describes the development and full-scale trial of two methods for removal of radioactive contamination on the surfaces of CAGR gas circulator components. The two methods described are a particle impact cleaning (PIC) decontamination technique and an electrochemical technique, 'electro-swabbing', which is based on the principle of decontamination by electro-polishing. In developing these techniques it was necessary to take account of the physical and chemical nature of the surface deposits on the gas circulator components; these were shown to consist of magnetite-type oxide and carbonaceous material. In order to follow the progress of the decontamination it was also necessary to develop a surface sampling technique which was effective and precise under these conditions; an electrochemical technique, employing similar principles to the electro-swabbing process, was developed for this purpose. The full-scale trial of the PIC decontamination technique was carried out on an inlet guide vane (IGV) assembly, this having been identified as the component from the gas circulator which contributes most to the radiation dose accumulated during routine circulator maintenance. The technique was shown to be practically viable and some 99% of the radioactive contamination was readily removed from the treated surfaces with only negligible surface damage being caused. The full-scale trial of the electro-swabbing decontamination technique was carried out on a gas circulator impeller. High decontamination factors were again achieved with ≥ 99% of the radioactive contamination being removed from the treated surfaces. The technique has practical limitations in terms of handling and treatment of waste-arisings. However, the use of specially-designed swabbing electrodes may allow the treatment of constricted geometries inaccessible to techniques such as PIC. The technique is also highly suitable for the treatment of soft-finish materials and of components fabricated from a

HB-LINE ANION EXCHANGE PURIFICATION OF AFS-2 PLUTONIUM FOR MOX

Energy Technology Data Exchange (ETDEWEB)

Kyser, E.; King, W.

2012-04-25

Non-radioactive cerium (Ce) and radioactive plutonium (Pu) anion exchange column experiments using scaled HB-Line designs were performed to investigate the feasibility of using either gadolinium nitrate (Gd) or boric acid (B as H{sub 3}BO{sub 3}) as a neutron poison in the H-Canyon dissolution process. Expected typical concentrations of probable impurities were tested and the removal of these impurities by a decontamination wash was measured. Impurity concentrations are compared to two specifications - designated as Column A or Column B (most restrictive) - proposed for plutonium oxide (PuO{sub 2}) product shipped to the Mixed Oxide (MOX) Fuel Fabrication Facility (MFFF). Use of Gd as a neutron poison requires a larger volume of wash for the proposed Column A specification. Since boron (B) has a higher proposed specification and is more easily removed by washing, it appears to be the better candidate for use in the H-Canyon dissolution process. Some difficulty was observed in achieving the Column A specification due to the limited effectiveness that the wash step has in removing the residual B after {approx}4 BV's wash. However a combination of the experimental 10 BV's wash results and a calculated DF from the oxalate precipitation process yields an overall DF sufficient to meet the Column A specification. For those impurities (other than B) not removed by 10 BV's of wash, the impurity is either not expected to be present in the feedstock or process, or recommendations have been provided for improvement in the analytical detection/method or validation of calculated results. In summary, boron is recommended as the appropriate neutron poison for H-Canyon dissolution and impurities are expected to meet the Column A specification limits for oxide production in HB-Line.

HB-LINE ANION EXCHANGE PURIFICATION OF AFS-2 PLUTONIUM FOR MOX

Energy Technology Data Exchange (ETDEWEB)

Kyser, E. A.; King, W. D.

2012-07-31

Non-radioactive cerium (Ce) and radioactive plutonium (Pu) anion exchange column experiments using scaled HB-Line designs were performed to investigate the feasibility of using either gadolinium nitrate (Gd) or boric acid (B as H{sub 3}BO{sub 3}) as a neutron poison in the H-Canyon dissolution process. Expected typical concentrations of probable impurities were tested and the removal of these impurities by a decontamination wash was measured. Impurity concentrations are compared to two specifications - designated as Column A or Column B (most restrictive) - proposed for plutonium oxide (PuO{sub 2}) product shipped to the Mixed Oxide (MOX) Fuel Fabrication Facility (MFFF). Use of Gd as a neutron poison requires a larger volume of wash for the proposed Column A specification. Since boron (B) has a higher proposed specification and is more easily removed by washing, it appears to be the better candidate for use in the H-Canyon dissolution process. Some difficulty was observed in achieving the Column A specification due to the limited effectiveness that the wash step has in removing the residual B after ~4 BV's wash. However a combination of the experimental 10 BV's wash results and a calculated DF from the oxalate precipitation process yields an overall DF sufficient to meet the Column A specification. For those impurities (other than B) not removed by 10 BV's of wash, the impurity is either not expected to be present in the feedstock or process, or recommendations have been provided for improvement in the analytical detection/method or validation of calculated results. In summary, boron is recommended as the appropriate neutron poison for H-Canyon dissolution and impurities are expected to meet the Column A specification limits for oxide production in HB-Line.

Breeding and plutonium characterization analysis on actinides closed water-cooled thorium reactor

International Nuclear Information System (INIS)

Permana, Sidik; Sekimoto, Hiroshi; Takaki, Naoyuki

2009-01-01

Higher difficulties (barrier) or more complex design of nuclear weapon, material fabrication and handling and isotopic enrichment can be achieved by a higher isotopic barrier. The isotopic material barrier includes critical mass, heat-generation rate, spontaneous neutron generation and radiation. Those isotopic barriers in case of plutonium isotope is strongly depend on the even mass number of plutonium isotope such as 238 Pu, 240 Pu and 242 Pu and for 233 U of thorium cycle depends on 232 U. In this present study, fuel sustainability as fuel breeding capability and plutonium characterization as main focus of proliferation resistance analysis have been analyzed. Minor actinide (MA) is used as doping material to be loaded into the reactors with thorium fuel. Basic design parameters are based on actinide closed-cycle reactor cooled by heavy water. The evaluation use equilibrium burnup analysis coupled with cell calculation of SRAC and nuclear data library is JENDL.32. Parametrical survey has been done to analyze the effect of MA doping rate, different moderation ratio for several equilibrium burnup cases. Plutonium characterization which based on plutonium isotope composition is strongly depending on MA doping concentration and different moderation conditions. Breeding condition can be achieved and high proliferation resistance level can be obtained by the present reactor systems. Higher isotopic plutonium composition of Pu-238 (more than 40%) can be obtained compared with other plutonium isotopes. In addition, higher moderation ratio gives the isotope composition of 238 Pu increases, however, it obtains lower composition when MA doping is increased and it slightly lower composition for higher burnup. Meanwhile, higher 240 Pu composition can be achieved by higher MA doping rate as well as for obtaining higher breeding capability. (author)

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)

Improvements in the detection of airborne plutonium

International Nuclear Information System (INIS)

Ryden, D.J.

1981-02-01

It is shown how it is possible to compensate individually for each of the background components on the filter paper used to collect samples. Experimentally it has been shown that the resulting compensated background count-rate averages zero with a standard deviation very close to the fundamental limit set by random statistical variations. Considerable improvements in the sensitivity of detecting airborne plutonium have been achieved. Two new plutonium-in-air monitors which use the compensation schemes described in this report are now available. Both have operated successfully in high concentrations of radon daughters. (author)

Coolant system decontamination

International Nuclear Information System (INIS)

Anstine, L.D.; James, D.B.; Melaika, E.A.; Peterson, J.P.

1981-01-01

An improved method for decontaminating the coolant system of water cooled nuclear power reactors and for regenerating the decontamination solution is described. A small amount of one or more weak-acid organic complexing agents is added to the reactor coolant, and the pH is adjusted to form a decontamination solution which is circulated throughout the coolant system to dissolve metal oxides from the interior surfaces and complex the resulting metal ions and radionuclide ions. The coolant containing the complexed metal ions and radionuclide ions is passed through a strong-base anion exchange resin bed which has been presaturated with a solution containing the complexing agents in the same ratio and having the same pH as the decontamination solution. As the decontamination solution passes through the resin bed, metal-complexed anions are exchanged for the metal-ion-free anions on the bed, while metal-ion-free anions in the solution pass through the bed, thus removing the metal ions and regenerating the decontamination solution. (author)

Characterization of decontamination and decommissioning wastes expected from the major processing facilities in the 200 Areas

International Nuclear Information System (INIS)

Amato, L.C.; Franklin, J.D.; Hyre, R.A.; Lowy, R.M.; Millar, J.S.; Pottmeyer, J.A.; Duncan, D.R.

1994-08-01

This study was intended to characterize and estimate the amounts of equipment and other materials that are candidates for removal and subsequent processing in a solid waste facility when the major processing and handling facilities in the 200 Areas of the Hanford Site are decontaminated and decommissioned. The facilities in this study were selected based on processing history and on the magnitude of the estimated decommissioning cost cited in the Surplus Facilities Program Plan; Fiscal Year 1993 (Winship and Hughes 1992). The facilities chosen for this study include B Plant (221-B), T Plant (221-T), U Plant (221-U), the Uranium Trioxide (UO 3 ) Plant (224-U and 224-UA), the Reduction Oxidation (REDOX) or S Plant (202-S), the Plutonium Concentration Facility for B Plant (224-B), and the Concentration Facility for the Plutonium Finishing Plant (PFP) and REDOX (233-S). This information is required to support planning activities for current and future solid waste treatment, storage, and disposal operations and facilities

Characterization of decontamination and decommissioning wastes expected from the major processing facilities in the 200 Areas

Energy Technology Data Exchange (ETDEWEB)

Amato, L.C.; Franklin, J.D.; Hyre, R.A.; Lowy, R.M.; Millar, J.S.; Pottmeyer, J.A. [Los Alamos Technical Associates, Kennewick, WA (United States); Duncan, D.R. [Westinghouse Hanford Co., Richland, WA (United States)

1994-08-01

This study was intended to characterize and estimate the amounts of equipment and other materials that are candidates for removal and subsequent processing in a solid waste facility when the major processing and handling facilities in the 200 Areas of the Hanford Site are decontaminated and decommissioned. The facilities in this study were selected based on processing history and on the magnitude of the estimated decommissioning cost cited in the Surplus Facilities Program Plan; Fiscal Year 1993 (Winship and Hughes 1992). The facilities chosen for this study include B Plant (221-B), T Plant (221-T), U Plant (221-U), the Uranium Trioxide (UO{sub 3}) Plant (224-U and 224-UA), the Reduction Oxidation (REDOX) or S Plant (202-S), the Plutonium Concentration Facility for B Plant (224-B), and the Concentration Facility for the Plutonium Finishing Plant (PFP) and REDOX (233-S). This information is required to support planning activities for current and future solid waste treatment, storage, and disposal operations and facilities.

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

International Nuclear Information System (INIS)

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

1979-08-01

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

How much plutonium does North Korea really have?

International Nuclear Information System (INIS)

Dreicer, J.S.

1997-01-01

In a previous study, as part of the Global Nuclear Material Control Model effort, the author estimated the maximum quantity of plutonium that could be produced in thermal research reactors in the potential nuclear weapon states (including North Korea), based on their declared power level. D. Albright has estimated the amount of plutonium the North Koreans may have produced since 1986 in the 5-megawatt-electric power reactor at Yongbon. Albright provided an upper-bound estimate of 53 kilograms of weapon-grade plutonium produced cumulatively if the gas-graphite (magnox) reactor had achieved a load factor of 0.80. This cumulative estimate of 53 kilograms ignores the potential plutonium production in the 8-megawatt-thermal research reactor, IRT-DPRK. To better quantify the cumulative North Korean production, the author conducted a study to estimate the amount of plutonium that could have been produced in the IRT-DPRK research reactor operating at the declared power level during the entire period it has operated, including a period it was not safeguarded. The author estimates that, at most, an additional 6 to 33 kilograms of plutonium could have been produced cumulatively in the research reactor operating at the declared power level during the entire period it has operated, including a 12-year period it was not safeguarded, resulting in a total of 13 to 47 kilograms of plutonium possibly produced in both the research and power reactors

Plutonium

International Nuclear Information System (INIS)

Anon.

1995-01-01

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

Learning more about plutonium

International Nuclear Information System (INIS)

2005-01-01

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

Long-term logistic analysis of FBR introduction strategy: avoiding both uranium and plutonium shortage

International Nuclear Information System (INIS)

Suzuki, T.

1995-01-01

Despite comfortable predictions on short to mid-term uranium resources, there is still a concern about long-term availability of competitive uranium resources. In order to achieve substantial uranium saving, early introduction of Fast Breeder Reactor (FBR) is desirable. But it is also known that rapid introduction of FBR could result in plutonium storage. Will there be enough plutonium on a global scale to sustain fast FBR growth? is there any other way to save uranium resource? This paper concludes that multi-option strategies to achieve flexible long-term strategy to avoid both uranium and plutonium storage are desirable. (authors)

Weapons-grade plutonium dispositioning. Volume 3: A new reactor concept without uranium or thorium for burning weapons-grade plutonium

International Nuclear Information System (INIS)

Ryskamp, J.M.; Schnitzler, B.G.; Fletcher, C.D.

1993-06-01

The National Academy of Sciences (NAS) requested that the Idaho National Engineering Laboratory (INEL) examine concepts that focus only on the destruction of 50,000 kg of weapons-grade plutonium. A concept has been developed by the INEL for a low-temperature, low-pressure, low-power density, low-coolant-flow-rate light water reactor that destroys plutonium quickly without using uranium or thorium. This concept is very safe and could be designed, constructed, and operated in a reasonable time frame. This concept does not produce electricity. Not considering other missions frees the design from the paradigms and constraints used by proponents of other dispositioning concepts. The plutonium destruction design goal is most easily achievable with a large, moderate power reactor that operates at a significantly lower thermal power density than is appropriate for reactors with multiple design goals. This volume presents the assumptions and requirements, a reactor concept overview, and a list of recommendations. The appendices contain detailed discussions on plutonium dispositioning, self-protection, fuel types, neutronics, thermal hydraulics, off-site radiation releases, and economics

Decontamination and decommissioning waste characterization and cost estimates from historical records

International Nuclear Information System (INIS)

Hootman, H.E.

1994-01-01

There are more than 600 facilities at the Savannah River Site (SRS) that are contaminated with either radioactivity, hazardous chemicals, or asbestos. The more significant facilities can be separated into broad categories for decontamination and decommissioning (D ampersand D) planning such as plutonium facilities, waste tanks, chemical separations canyons, and nuclear reactors. Uncertainties exist in the timing, extent of stabilization, and D ampersand D required for these production facilities. Detailed analyses of the risk, costs, and engineering feasibility are needed to define production facility end states to ensure expected reduction in health and environmental risk. In the meantime, scoping projections are required to satisfy Department of Energy (DOE) requirements for 30 year plans, and to indicate where detailed analysis should be funded

Chemical decontamination solutions: Effects on PWR equipment

International Nuclear Information System (INIS)

Pezze, C.M.; Colvin, E.R.; Aspden, R.G.

1992-01-01

A critical objective for the nuclear industry is the reduction of personnel exposure to radiation. Reductions have been achieved through industry's radiation management programs including training and radiation awareness concepts. Increased plant maintenance and higher radiation fields at many sites continue to raise concerns. To alleviate the radiation exposure problem, the sources of radiation which contribute to personnel exposure must be removed from the plant. A feasible was of significantly reducing these sources from a Pressurized Water Reactor (PWR) is to chemically decontaminate the entire reactor coolant system (RCS). A program was conducted to determine the technical acceptability of using certain dilute chemical solvent processes for full RCS chemical decontamination. The two processes evaluated were CAN-DEREM and LOMI. The purpose of the program was to define and complete a systematic evaluation of the major issues that need to be addressed for the successful decontamination of the entire RCS and affected portions of the auxiliary systems of a four-loop PWR system. A test program was designed to evaluate the corrosion effects of the two decontamination processes under expected plant conditions. Materials and sample configurations dictated by generic PWR components were evaluated. The testing also included many standard corrosion coupons. The test data were then used to assess the impact of chemical decontamination on the physical condition and operability of the components, equipment and mechanical systems that make up the RCS. An overview of the test program, sample configurations, data and engineering evaluations is presented. The data demonstrate that through detailed engineering evaluations of corrosion data and equipment function, the impact of full RCS chemical decontamination on plant equipment is established

A decontamination technique for decommissioning waste

International Nuclear Information System (INIS)

Heki, H.; Hosaka, K.; Kuribayashi, N.; Ishikura, T.

1993-01-01

A large amount of radioactive metallic waste is generated from decommissioned commercial nuclear reactors. It is necessary from the point of environmental protection and resource utilization to decontaminate the contaminated metallic waste. A decommissioning waste processing system has been previously proposed considering such decommissioning waste characteristics as its large quantity, large radioactivity range, and various shapes and materials. The decontamination process in this system was carried out by abrasive blasting as pretreatment, electrochemical decontamination as the main process, and ultrasonic cleaning in water as post-treatment. For electrochemical decontamination, electrolytic decontamination for simple shaped waste and REDOX decontamination for complicated shaped waste were used as effective decontamination processing. This time, various kinds of actual radioactive contaminated samples were taken from operating power plants to simulate the decontamination of decommissioning waste. After analyzing the composition, morphogenesis and surface observation, electrolytic decontamination, REDOX decontamination, and ultrasonic cleaning experiments were carried out by using these samples. As a result, all the samples were decontaminated below the assumed exemption level(=4 x 10 -2 Bq/g). A maximum decontamination factor of over 104 was obtained by both electrolytic and REDOX decontamination. The stainless steel sample was easy to decontaminate in both electrochemical decontaminations because of its thin oxidized layer. The ultrasonic cleaning process after electrochemical decontamination worked effectively for removing adhesive sludge and the contaminated liquid. It has been concluded from the results mentioned above that electrolytic decontamination and REDOX decontamination are effective decontamination process for decontaminating decommissioning waste

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.)

Effect of cooling rate on achieving thermodynamic equilibrium in uranium-plutonium mixed oxides

Science.gov (United States)

Vauchy, Romain; Belin, Renaud C.; Robisson, Anne-Charlotte; Hodaj, Fiqiri

2016-02-01

In situ X-ray diffraction was used to study the structural changes occurring in uranium-plutonium mixed oxides U1-yPuyO2-x with y = 0.15; 0.28 and 0.45 during cooling from 1773 K to room-temperature under He + 5% H2 atmosphere. We compare the fastest and slowest cooling rates allowed by our apparatus i.e. 2 K s-1 and 0.005 K s-1, respectively. The promptly cooled samples evidenced a phase separation whereas samples cooled slowly did not due to their complete oxidation in contact with the atmosphere during cooling. Besides the composition of the annealing gas mixture, the cooling rate plays a major role on the control of the Oxygen/Metal ratio (O/M) and then on the crystallographic properties of the U1-yPuyO2-x uranium-plutonium mixed oxides.

Decontaminating agents and decontamination processes for nuclear industry and for plant demolition

International Nuclear Information System (INIS)

Henning, Klaus; Gojowczyk, Peter

2012-01-01

Decontamination of surfaces of materials in nuclear facilities or in nuclear power plants under demolition can be carried out successfully if surface treatment is performed by dipping or in an ultrasonic bath by alternating between alkaline and acid baths with intermediate rinsing in demineralized water. Decontaminating aluminium surfaces sensitive to corrosion requires further treatment in an ultrasonic bath, after the first 2 ultrasonic baths, with a weak alkaline decontaminating agent. This applies alike to components to be decontaminated for re-use and parts of materials to be disposed of. The decontamination action depends on the surfaces either being free from corrosion or else showing pronounced corrosion. (orig.)

Modeling lung cancer risks in laboratory dogs exposed to inhaled plutonium

International Nuclear Information System (INIS)

Gilbert, E.S.; Park, J.F.; Buschbom, R.L.

1990-06-01

These analyses are based on data from a lifespan study of beagle dogs exposed to inhaled plutonium being conducted at Pacific Northwest Laboratory. An important goal of this study is to increase understanding of health risk resulting from this exposure, with particular attention to lung cancer risks. Data on humans exposed to plutonium are inadequate for achieving this goal

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

Lessons Learned from Decontamination Experiences

Energy Technology Data Exchange (ETDEWEB)

Sorensen, JH

2000-11-16

This interim report describes a DOE project currently underway to establish what is known about decontamination of buildings and people and the procedures and protocols used to determine when and how people or buildings are considered ''clean'' following decontamination. To fulfill this objective, the study systematically examined reported decontamination experiences to determine what procedures and protocols are currently employed for decontamination, the timeframe involved to initiate and complete the decontamination process, how the contaminants were identified, the problems encountered during the decontamination process, how response efforts of agencies were coordinated, and the perceived social psychological effects on people who were decontaminated or who participated in the decontamination process. Findings and recommendations from the study are intended to aid decision-making and to improve the basis for determining appropriate decontamination protocols for recovery planners and policy makers for responding to chemical and biological events.

Decontamination of body surface

International Nuclear Information System (INIS)

Harase, Chieko.

1989-01-01

There are two important points for an effective application of decontamination procedures. One is the organizing method of responsible decontamination teams. The team should be directed by medical doctor with the knowledge of decontamination of radionuclides. The other point is the place of application of the decontamination. Hospitals and clinics, especially with a department of nuclear medicine, or specialized units such as an emergency medical center are preferable. Before decontamination procedures are initiated, adequate monitoring of the body surface should be undertaken by a competent person in order to demarcate the areas which are contaminated. There are fundamental principles which are applicable to all decontamination procedures. (1) Precautions must always be taken to prevent further spread of contamination during decontamination operations. (2) Mild decontamination methods should be tried before resorting to treatment which can damage the body surface. The specific feature of each contamination varies widely in radionuclides involved, place and area of the contamination, condition of the contaminated skin such as whether the skin is wounded or not, and others. Soap and water are usually good detergents in most cases. If they fail, orange oil cream (SUPERDECONCREAM, available from Tokyo Engineering Co.) specially prepared for decontamination of radionuclides of most fission and corrosion products may be used. Contaminated hair should be washed several times with an efficient shampoo. (author)

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

Application of a modified electrochemical system for surface decontamination of radioactive metal waste

International Nuclear Information System (INIS)

Lee, J.H.; Lim, Y.K.; Yang, H.Y.; Shin, S.W.; Song, M.J.

2003-01-01

Conventional and modified electrolytic decontamination experiments were performed in a solution of sodium sulfate for the decontamination of carbon steel as the simulated metal wastes which are generated in large amounts from nuclear power plants. The effect of reaction time, current density and concentration of electrolytes in the modified electrolytic decontamination system were examined to remove the surface contamination of the simulated radioactive metal wastes. As for the results of this research, the modified electrochemical decontamination process can decontaminate more effectively than the conventional decontamination process by applying different anode material which causes higher induced electro-motive forces. When 0.5 M sodium sulfate, 0.4 A/cm 2 current density and 30 minutes reaction time were applied in the modified process, a 16 μm thickness change that is expected to remove most surface contamination in radioactive metal wastes was achieved on carbon steel which is the main material of radioactive metal waste in nuclear power plants. The decontamination efficiency of metal waste showed similar results with the small and large lab-scale modified electrochemical system. The application of this modified electrolytic decontamination system is expected to play a considerable role for decontamination of radioactive metal waste in nuclear power plants in the near future. (author)

Separation of plutonium oxide nanoparticles and colloids

Energy Technology Data Exchange (ETDEWEB)

Wilson, Richard E.; Skanthakumar, S.; Soderholm, L. [Argonne National Laboratory, IL (United States). Chemical Sciences and Engineering Division

2011-11-18

Colloidal plutonium is an important component of Pu aqueous speciation. Pu colloids are problematic in nuclear separations and are a potential transport vector in the environment. Using a mixture of n-octanol and trichloroacetic acid a selective and reversible separation of these particles can be achieved by exploiting their surface reactivity. [German] Kolloidales Plutonium ist ein wichtiger Bestandteil in waessrigen Pu-Bereitungen. Pu-Kolloide sind problematisch bei der Wiederaufbereitung von Kernmaterial und bilden einen potenziellen Transportvektor in die Umwelt. Mit einem Loesungsmittelgemisch aus n-Octanol und Trichloressigsaeure gelingt die selektive und reversible Trennung dieser Partikel durch Ausnutzung ihrer Oberflaechenreaktivitaet.

Dry decontamination for tritiated wastes

International Nuclear Information System (INIS)

Shi Zhengkun; Wu Tao; Dan Guiping; Xie Yun

2009-01-01

To aim at decontamination of tritiated wastes, we have developed and fabricated a dry tritium decontamination system, which is designed to reduce tritium surface contamination of various alloy by UV, ozone and heating. The result indicates that the elevation of temperature can obviously improve decontamination effect. With 3 h irradiation by 365 nm UV at 220 degree C, it has a decontamination rate of 99% to stainless steel surface. Ozone can more obviously improve decontamination effect when metal was heated. Ozone has a decontamination effect beyond 95% to stainless steel, aluminum and brass at 220 degree C. Tritium surface concentration of metal has a little increase after decontamination. (authors)

Ontario Hydro decontamination experience

Energy Technology Data Exchange (ETDEWEB)

Lacy, C S; Patterson, R W; Upton, M S [Chemistry and Metallurgy Department, Central Production Services, Ontario Hydro, ON (Canada)

1991-04-01

Ontario Hydro currently operates 18 nuclear electric generating units of the CANDU design with a net capacity of 12,402 MW(e). An additional 1,762 MW(e) is under construction. The operation of these facilities has underlined the need to have decontamination capability both to reduce radiation fields, as well as to control and reduce contamination during component maintenance. This paper presents Ontario Hydro decontamination experience in two key areas - full heat transport decontamination to reduce system radiation fields, and component decontamination to reduce loose contamination particularly as practised in maintenance and decontamination centres. (author)

Ontario Hydro decontamination experience

International Nuclear Information System (INIS)

Lacy, C.S.; Patterson, R.W.; Upton, M.S.

1991-01-01

Ontario Hydro currently operates 18 nuclear electric generating units of the CANDU design with a net capacity of 12,402 MW(e). An additional 1,762 MW(e) is under construction. The operation of these facilities has underlined the need to have decontamination capability both to reduce radiation fields, as well as to control and reduce contamination during component maintenance. This paper presents Ontario Hydro decontamination experience in two key areas - full heat transport decontamination to reduce system radiation fields, and component decontamination to reduce loose contamination particularly as practised in maintenance and decontamination centres. (author)

Gross decontamination experiment report

International Nuclear Information System (INIS)

Mason, R.; Kinney, K.; Dettorre, J.; Gilbert, V.

1983-07-01

A Gross Decontamination Experiment was conducted on various levels and surfaces of the TMI - Unit 2 reactor building in March 1982. The polar crane, D-rings, missile shields, refueling canals, refueling bridges, equipment, and elevations 305' and 347'-6'' were flushed with low pressure water. Additionally, floor surfaces on elevation 305' and floor surfaces and major pieces of equipment on elevation 347'-6'' were sprayed with high pressure water. Selective surfaces were decontaminated with a mechanical scrubber and chemicals. Strippable coating was tested and evaluated on equipment and floor surfaces. The effectiveness, efficiency, and safety of several decontamination techniques were established for the large, complex decontamination effort. Various decontamination equipment was evaluated and its effectiveness was documented. Decontamination training and procedures were documented and evaluated, as were the support system and organization for the experiment

Gross decontamination experiment report

Energy Technology Data Exchange (ETDEWEB)

Mason, R.; Kinney, K.; Dettorre, J.; Gilbert, V.

1983-07-01

A Gross Decontamination Experiment was conducted on various levels and surfaces of the TMI - Unit 2 reactor building in March 1982. The polar crane, D-rings, missile shields, refueling canals, refueling bridges, equipment, and elevations 305' and 347'-6'' were flushed with low pressure water. Additionally, floor surfaces on elevation 305' and floor surfaces and major pieces of equipment on elevation 347'-6'' were sprayed with high pressure water. Selective surfaces were decontaminated with a mechanical scrubber and chemicals. Strippable coating was tested and evaluated on equipment and floor surfaces. The effectiveness, efficiency, and safety of several decontamination techniques were established for the large, complex decontamination effort. Various decontamination equipment was evaluated and its effectiveness was documented. Decontamination training and procedures were documented and evaluated, as were the support system and organization for the experiment.

Decontamination of transvaginal ultrasound probes: Review of national practice and need for national guidelines

International Nuclear Information System (INIS)

Gray, R.A.; Williams, P.L.; Dubbins, P.A.; Jenks, P.J.

2012-01-01

Aim: To determine the national practice of transvaginal ultrasound (TVUS) probe decontamination in English hospitals and to develop recommendations for guidance. Materials and methods: A literature review was undertaken to clarify best practice and evaluate methods of decontamination of TVUS probes. A questionnaire was developed to ascertain TVUS probe decontamination programmes in current use within English hospitals. This was sent to ultrasound leads of 100 English hospitals; 68 hospitals responded. Results: There is a wide variation in TVUS probe decontamination across English hospitals. Although the majority of respondents (87%, 59/68) reported having clear and practical written guidelines for TVUS decontamination, the frequency, methods, and types of decontamination solutions utilized were widely variable and none meet the standards required to achieve high-level disinfection. Conclusion: While the decontamination of other endoluminal medical devices (e.g., flexible endoscopes) is well defined and regulated, the decontamination of TVUS probes has no such guidance. There appears to be incomplete understanding of the level of risk posed by TVUS probes, and in some cases, this has resulted in highly questionable practices regarding TVUS hygiene. There is an urgent need to develop evidence-based national guidance for TVUS probe decontamination.

New techniques available for decontamination

International Nuclear Information System (INIS)

Costes, J.R.; Cochaux, C.

1996-01-01

As nuclear industry dismantling operations become more widespread, one naturally sees the growth of specific needs in decontamination techniques. In this paper, the authors present two applications involving the decategorization of wastes from dismantling. Decategorization means using decontamination to transform the wastes into a lower, and thus cheaper, category. The first application is in decategorizing large mild steel pipes, which come from the stage decommissioning of the G2/G3 graphite gas reactors at Marcoule. A large number of these pipes (4000 t) have been contaminated by deposits and encrustations of 60 Co (95%) and 137 Cs (5%) to the extent of 200 Bq/cm 2 . The objective was to avoid having to store them on surface sites for 300 yr. This is achieved by decontaminating them to a level that enables the metal to be reused. The other application involves stainless steel waste cut into small sections, which comes from the stage decommissioning of a radiometallurgy laboratory (RM2) at Fontenay aux Roses. This waste was not acceptable to the surface storage center due to high levels of alpha contamination. A decategorization technique has been developed for part of the 13 tonnes of waste concerned, which avoids the need for it to be disposed of in extremely costly geologic repositories

Toshiba's decontamination technologies for the decommissioning

International Nuclear Information System (INIS)

Inoue, Yuki; Yaita, Yumi; Sakai, Hitoshi

2011-01-01

For the decommissioning, two types of decontamination process are necessary, 1) system decontamination before dismantling and 2) decontamination of dismantling waste. Toshiba has been developing the decontamination technologies for the both purposes from the viewpoint of minimizing the secondary waste. For the system decontamination before dismantling, chemical decontamination process, such as T-OZON, can be applicable for stainless steel or carbon steel piping. For the decontamination of dismantling waste, several types of process have been developed to apply variety of shapes and materials. For the simple shape materials, physical decontamination process, such as blast decontamination, is effective. We have developed new blast decontamination process with highly durable zirconia particle. It can be used repeatedly and secondary waste can be reduced compared with conventional blast particle. For the complex shape materials, chemical decontamination process can be applied that formic acid decontamination process for carbon steel and electrolytic reduction decontamination process with organic acid for stainless steel. These chemicals can be decomposed to carbon dioxide and water and amount of secondary waste can be small. (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)

Decontamination sheet

International Nuclear Information System (INIS)

Hirose, Emiko; Kanesaki, Ken.

1995-01-01

The decontamination sheet of the present invention is formed by applying an adhesive on one surface of a polymer sheet and releasably appending a plurality of curing sheets. In addition, perforated lines are formed on the sheet, and a decontaminating agent is incorporated in the adhesive. This can reduce the number of curing operation steps when a plurality steps of operations for radiation decontamination equipments are performed, and further, the amount of wastes of the cured sheets, and operator's exposure are reduced, as well as an efficiency of the curing operation can be improved, and propagation of contamination can be prevented. (T.M.)

Development of decontamination methods

International Nuclear Information System (INIS)

Kunze, S.; Dippel, T.; Hentschel, D.

1976-01-01

PVC floorings, fabricated by mixing of the basic components, showed no relation between content of fillers and decontamination results. Decontamination results are partly poorer, if the flooring contains a high concentration of the filler, especially if the latter consists mainly of hydrophilic materials. The coloring of the floorings seems to have no influence on the decontamination. Rubber floorings, fabricated by chemical reactions between polymers, vulcanization materials and fillers, show decontamination results depending definitely from the proper choice of the filler. Flooring types, containing lampblack, graphite, kaoline, barium sulfate and titanium oxide are easy to decontaminate. Increasing contents of hydrophilic filler cause a fall off in the decontamination results. The decontamination effectiveness and the homogenity of cleaning pastes based on hydrochloric acid, nitric acid, titanium oxide and polyethylene powders is strongly depended on the content of hydrochloric acid. Reduction of the content of this component to less than 2 w/O remains the effectiveness unchanged only if the titanium oxide-polyethylene powder mixture is substituted by a high density, highly surface active powder material. This type of paste containing no hydrochloric acid shows nearly the same decontamination effectiveness as standard pickling pastes containing about 30% hydrochlorid acid. Properly prepared salt powder turn out to be easily and successfully applied to metal surfaces by a flame spray technique. The thin layer of molten salts is a very effective decontamination to samples contaminated in the primary loop of a PWR. (orig.) [de

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)

Decontamination and provenance tracking. The key to acceptable recycle of nuclear materials

International Nuclear Information System (INIS)

Bradbury, D.; Elder, G.R.; Wood, C.J.

2002-01-01

Decommissioning of nuclear plants and components demands the proper management of the process, both for economic reasons and for retaining public confidence in the continued use of nuclear power. Surface decontamination has an important role to play in decommissioning. A new development, the EPRI DFDX process, produces secondary waste from decontamination in the form of powdered metal rather than ion exchange resin, thereby reducing the volume of secondary waste for storage and eventual disposal. The process has been patented and licensed and is due to be field-tested on a number of sites starting in 2002. Although the purpose of the process is to clean materials sufficiently to achieve unrestricted release, in practice there is some public unease at the prospect of formerly contaminated materials passing into unrestricted use. Greater public support for recycle can be achieved by recording the provenance of decontaminated materials and recycling them back into restricted uses in the nuclear industry. Because the materials have first been decontaminated to below free release levels, there is no objection to using non-radioactive facilities for the recycling and manufacturing activities, provided that the materials are properly tracked to prevent their uncontrolled release. (author)

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.

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

International Nuclear Information System (INIS)

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

1985-01-01

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

High-temperature enthalpies of plutonium monocarbide and plutonium sesquicarbide

International Nuclear Information System (INIS)

Oetting, F.L.

1979-01-01

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

Concerning temporary method for return transport of plutonium

International Nuclear Information System (INIS)

1990-01-01

One of the urgent matters under deliberation in the Working Group for Nuclear Fuel Cycle, Atomic Energy Comission of Japan, is to develop a method for smooth and safe transport of plutonium to be returned from Britain and France, where spent fuel sent from Japan is reprocessed by contract. Return transport of plutonium from these nations will start in 1992. Preparatory work has been conducted in Japan for air transport of plutonium, which is to be used by Power Reactor and Nuclear Fuel Development Corporation. For this, efforts have been made since 1984 to develop containers for air transport of plutonium. Though the corporation will continue research, it will take considerable time until practical containers are developed, so the material have to be transported by sea for the time being. The corporation should play the leading role in conducting the return transport operation in cooperation with other organizations concerned including power companies. To achieve this, the corporation should be active in making preparations including the development of transport plans. (N.K.)

Decontamination method

International Nuclear Information System (INIS)

Tsujimura, Hiroshi; Ono, Shigeki; Tada, Nobuo; Tamai, Yasumasa; Okada, Masaya; Kurihara, Masayuki; Onuki, Toyomitsu; Toyota, Seiichi

1998-01-01

Before contamination of materials to be decontaminated, a surface of a region where a strippable paint is to be coated is smoothed by an epoxy resin previously. Then, a waterproof sheet is extended to the material to be decontaminated, and the strippable paint is applied to the periphery or the entire surface of the sheet. In order to facilitate peeling, the strippable paint is not applied to a portion of the outer circumference of the sheet. Even if the contaminating circumstance is an air atmosphere or a liquid such as reactor water, since the sheet itself has waterproofness and the strippable paint excellent in gas and water tightness is applied to the periphery, contamination is eliminated. When decontaminating the material to be decontaminated having contaminated surfaces, if the sheet for the start of peeling is picked up and the sheet is peeled, the strippable paint at the periphery thereof can be peeled off together with the sheet. (N.H.)

Decontamination method

Energy Technology Data Exchange (ETDEWEB)

Tsujimura, Hiroshi; Ono, Shigeki; Tada, Nobuo; Tamai, Yasumasa; Okada, Masaya; Kurihara, Masayuki [Hitachi Ltd., Tokyo (Japan); Onuki, Toyomitsu; Toyota, Seiichi

1998-10-27

Before contamination of materials to be decontaminated, a surface of a region where a strippable paint is to be coated is smoothed by an epoxy resin previously. Then, a waterproof sheet is extended to the material to be decontaminated, and the strippable paint is applied to the periphery or the entire surface of the sheet. In order to facilitate peeling, the strippable paint is not applied to a portion of the outer circumference of the sheet. Even if the contaminating circumstance is an air atmosphere or a liquid such as reactor water, since the sheet itself has waterproofness and the strippable paint excellent in gas and water tightness is applied to the periphery, contamination is eliminated. When decontaminating the material to be decontaminated having contaminated surfaces, if the sheet for the start of peeling is picked up and the sheet is peeled, the strippable paint at the periphery thereof can be peeled off together with the sheet. (N.H.)

Influence of Decontamination

International Nuclear Information System (INIS)

Knaack, Michael

2016-01-01

This paper describes the influence of several decontamination techniques on the decommissioning of nuclear facilities. There are different kinds of decontamination methods like mechanical and chemical processes. The techniques specified, and their potential to change measured characteristics like the isotope vector of the contamination is demonstrated. It is common for all these processes, that the contamination is removed from the surface. Slightly adhered nuclides can be removed more effectively than strongly sticking nuclides. Usually a mixture of these nuclides forms the contamination. Problematically any kind of decontamination will influence the nuclide distribution and the isotope vector. On the one hand it is helpful to know the nuclide distribution and the isotope vector for the radiological characterization of the nuclear facility and on the other hand this information will be changed in the decontamination process. This is important especially for free release procedures, radiation protection and waste management. Some questions on the need of decontamination have been discussed. (authors)

Ultra-sensitive detection of plutonium by accelerator mass spectrometry

Energy Technology Data Exchange (ETDEWEB)

Fifield, L K; Cresswell, R G; Ophel, T R; Ditada, M [Australian National Univ., Canberra, ACT (Australia). Dept. of Nuclear Physics; Day, J P; Clacher, A [Manchester Univ. (United Kingdom). Dept. of Chemistry; Priest, N D [AEA Technology, Harwell (United Kingdom)

1997-12-31

On the bases of the measurements performed to date, a sensitivity of 10{sup 6} atoms is achievable with accelerator mass spectroscopy (AMS) for each of the plutonium isotopes. Not only does this open the way to the sort of study outlined, but it also makes possible other novel applications, of which two examples are given: (i)the ration of {sup 240}Pu to {sup 239}Pu as a sensitive indicator of the source of the plutonium; (ii) the biochemistry of plutonium in humans. The ultra-sensitive atom counting capability of AMS will make it possible to use the very long-lived {sup 244}Pu (8x10{sup 7}a) in human volunteer studies without any significant increase in radiation body burden. This paper will describe the AMS technique as applied to plutonium using the ANU`s 14UD accelerator, will present the results obtained to date, and will discuss the prospects for the future.

Ultra-sensitive detection of plutonium by accelerator mass spectrometry

Energy Technology Data Exchange (ETDEWEB)

Fifield, L.K.; Cresswell, R.G.; Ophel, T.R.; Ditada, M. [Australian National Univ., Canberra, ACT (Australia). Dept. of Nuclear Physics; Day, J.P.; Clacher, A. [Manchester Univ. (United Kingdom). Dept. of Chemistry; Priest, N.D. [AEA Technology, Harwell (United Kingdom)

1996-12-31

On the bases of the measurements performed to date, a sensitivity of 10{sup 6} atoms is achievable with accelerator mass spectroscopy (AMS) for each of the plutonium isotopes. Not only does this open the way to the sort of study outlined, but it also makes possible other novel applications, of which two examples are given: (i)the ration of {sup 240}Pu to {sup 239}Pu as a sensitive indicator of the source of the plutonium; (ii) the biochemistry of plutonium in humans. The ultra-sensitive atom counting capability of AMS will make it possible to use the very long-lived {sup 244}Pu (8x10{sup 7}a) in human volunteer studies without any significant increase in radiation body burden. This paper will describe the AMS technique as applied to plutonium using the ANU`s 14UD accelerator, will present the results obtained to date, and will discuss the prospects for the future.

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

International Nuclear Information System (INIS)

Hanus, D.; Kleykamp, H.

1982-01-01

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

Effect of cooling rate on achieving thermodynamic equilibrium in uranium–plutonium mixed oxides

Energy Technology Data Exchange (ETDEWEB)

Vauchy, Romain, E-mail: romain.vauchy@cea.fr [CEA, DEN, DTEC, Marcoule, 30207, Bagnols-sur-Cèze (France); CEA, DEN, DEC, Cadarache, 13108, Saint-Paul-lez-Durance (France); Belin, Renaud C.; Robisson, Anne-Charlotte [CEA, DEN, DEC, Cadarache, 13108, Saint-Paul-lez-Durance (France); Hodaj, Fiqiri [Univ. Grenoble Alpes, SIMAP, F-38000, Grenoble (France); CNRS, Grenoble INP, SIMAP, F-38000, Grenoble (France)

2016-02-15

In situ X-ray diffraction was used to study the structural changes occurring in uranium–plutonium mixed oxides U{sub 1−y}Pu{sub y}O{sub 2−x} with y = 0.15; 0.28 and 0.45 during cooling from 1773 K to room-temperature under He + 5% H{sub 2} atmosphere. We compare the fastest and slowest cooling rates allowed by our apparatus i.e. 2 K s{sup −1} and 0.005 K s{sup −1}, respectively. The promptly cooled samples evidenced a phase separation whereas samples cooled slowly did not due to their complete oxidation in contact with the atmosphere during cooling. Besides the composition of the annealing gas mixture, the cooling rate plays a major role on the control of the Oxygen/Metal ratio (O/M) and then on the crystallographic properties of the U{sub 1−y}Pu{sub y}O{sub 2−x} uranium–plutonium mixed oxides.

Skin contamination - prevention and decontaminating

International Nuclear Information System (INIS)

Henning, K.

2001-01-01

A detailed examination is made of the structure of human skin. Measures were drawn up to prevent skin contamination in nuclear installations as well as contaminated skin was decontaminated from the personnel. By systematically applying these measures a significant level of success was achieved in preventing contamination in nuclear installations. Cases where more far-reaching chemical methods had to be used were kept to a minimum. (R.P.)

Decontamination device for pipeline

International Nuclear Information System (INIS)

Harashina, Heihachi.

1994-01-01

Pipelines to be decontaminated are parts of pipelines contaminated with radioactive materials, and they are connected to a fluid transfer means (for example, a bladeless pump) and a ball collector by way of a connector. The fluid of a mixture of chemical decontaminating liquid and spheres is sent into pipelines to be decontaminated. The spheres are, for example, heat resistant porous hard or soft rubber spheres. The fluid discharged from the pipelines to be decontaminated are circulated by way of bypassing means. The inner surface of the pipelines is decontaminated by the circulation of the fluid. When the bypass means is closed, the fluid discharged from the pipelines to be decontaminated is sent to the ball collector, and the spheres are captured by a hopper. Further, the liquid is sent to the filtrating means to filter the chemical contaminating liquid, and sludges contained in the liquid are captured. (I.N.)

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

Plasma Decontamination of Uranium From the Interior of Aluminum Objects

International Nuclear Information System (INIS)

Veilleux, J.M.; Munson, C.; Fitzpatrick, J.; Chamberlin, E.P.; El-Genk, M.S.

1997-01-01

RF plasma glow discharges are being investigated for removing and recovering radioactive elements from contaminated objects, especially those contaminated with transuranic (TRU) materials. These plasmas, using nitrogen trifluoride as the working gas, have been successful at removing uranium and plutonium contaminants from test coupons of stainless steel and aluminum surfaces, including small cracks and crevices, and the interior surfaces of relatively hard to reach aluminum pipes. Contaminant removal exceeded 99.9% from simple surfaces and contaminant recovery using cryogenic traps has exceeded 50%. Work continues with the objective of demonstrating that transuranic contaminated waste can be transformed to low level waste (LLW) and to better understand the physics of the interaction between plasma and surface contaminants. This work summarizes the preliminary results from plasma decontamination from the interior of aluminum objects--the nooks and crannies experiments

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

Possibilities of soil washing for decontamination at Belgoprocess

Energy Technology Data Exchange (ETDEWEB)

Aerts, Wouter [Belgoprocess, Dessel, Antwerp (Belgium); De Bruecker, Thomas; Lytek, Anna [DEC - DEME Environmental Contractor, Zwijndrecht, Antwerp (Belgium)

2013-07-01

Contaminated soils form a large part of the nuclear waste arising from decommissioning activities. The storage and disposal of these large volumes of waste is costly. For this reason techniques which can decontaminate this waste stream to free release levels are economically very interesting. A feasibility study of the possibilities of soil washing to decontaminate such soils was ordered by NIRAS/ONDRAF and performed at Belgoprocess in collaboration with DEC. Initial contamination level and particle size distributions of contaminated soils from three different sources were determined. The main isotopes detected with gamma spectrometry contained in the waste were {sup 241}Am, {sup 137}Cs, {sup 226}Ra, {sup 60}Co and {sup 232}Th. The particle size distribution revealed that more than half of the mass of the quartz sand that makes up the soil has a particle size between 125 and 212 μm. This fraction is less contaminated than the fractions containing smaller particles. However, separation of the fines fraction (< 125 μm) was not enough to achieve the free release limit. Soil attrition was tested as an extra decontamination step for the sand fraction. The removal efficiencies for the different radionuclides contained in the soil were measured. The process conditions were optimized to achieve maximum removal and a treatment method for the secondary waste coming from this process step was determined. The soil washing process was not only performed with water but also with nitric acid to assess the possibilities of a combination of a mechanical and a chemical decontamination process. Reduction efficiencies of 60-80% for the most relevant radionuclides were recorded. (authors)

Comparison of four different fuller's earth formulations in skin decontamination.

Science.gov (United States)

Roul, Annick; Le, Cong-Anh-Khanh; Gustin, Marie-Paule; Clavaud, Emmanuel; Verrier, Bernard; Pirot, Fabrice; Falson, Françoise

2017-12-01

Industrial accidents, wars and terrorist threats are potential sources of skin contamination by highly toxic chemical warfare agents and manufacturing compounds. We have compared the time-dependent adsorption capacity and decontamination efficiency of fuller's earth (FE) for four different formulations for the molecular tracer, 4-cyanophenol (4-CP), in vitro and ex vivo using water decontamination as standard. The adsorption capacity of FE was assessed in vitro for 4-CP aqueous solutions whereas decontamination efficiency was investigated ex vivo by tracking porcine skin 4-CP content using attenuated total reflectance Fourier transform infrared spectroscopy. Decontamination was performed on short time, exposed porcine skin to 4-CP by application of FE: (1) as free powder; (2) loaded on adhesive tape; (3) on powdered glove; or (4) in suspension. Removal rate of 4-CP from aqueous solutions correlates with the amount of FE and its contact time. Decontamination efficiency estimated by the percentage of 4-CP recovery from contaminated porcine skin, achieved 54% with water, ranged between ~60 and 70% with dry FE and reached ~90% with FE suspension. Successful decontamination of the FE suspension, enabling a dramatic reduction of skin contamination after a brief exposure scenario, appears to be rapid, reliable and should be formulated in a new device ready to use for self-application. Copyright © 2017 John Wiley & Sons, Ltd.

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

Cleaning up the Legacy of the Cold War: Plutonium Oxides and the Role of Synchrotron Radiation Research

Energy Technology Data Exchange (ETDEWEB)

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

2015-01-21

The deceptively simple binary formula of AnO₂ belies an incredibly complex structural nature, and propensity to form mixed-valent, nonstoichiometric phases of composition AnO_2±x. For plutonium, the very formation of PuO_2+x has challenged a long-established dogma, and raised fundamental questions for long-term storage and environmental migration. This presentation covers two aspects of Los Alamos synchrotron radiation studies of plutonium oxides: (1) the structural chemistry of laboratory-prepared AnO_2+x systems (An = U, Pu; 0 ≤ x ≤ 0.25) determined through a combination of x-ray absorption fine structure spectroscopy (XAFS) and x-ray scattering of laboratory prepared samples; and (2) the application of synchrotron radiation towards the decontamination and decommissioning of the Rocky Flats Environmental Technology Site. Making the case for particle transport mechanisms as the basis of plutonium and americium mobility, rather than aqueous sorption-desorption processes, established a successful scientific basis for the dominance of physical transport processes by wind and water. The scientific basis was successful because it was in agreement with general theory on insolubility of PuO₂ in oxidation state IV, results of ultrafiltration analyses of field water/sediment samples, XAFS analyses of soil, sediment, and concrete samples, and was also in general agreement with on-site monitoring data. This understanding allowed Site contractors to rapidly move to application of soil erosion and sediment transport models as the means of predicting plutonium and americium transport, which led to design and application of site-wide soil erosion control technology to help control downstream concentrations of plutonium and americium in streamflow.

Cleaning up the Legacy of the Cold War: Plutonium Oxides and the Role of Synchrotron Radiation Research

International Nuclear Information System (INIS)

Clark, David Lewis

2015-01-01

The deceptively simple binary formula of AnO 2 belies an incredibly complex structural nature, and propensity to form mixed-valent, nonstoichiometric phases of composition AnO 2±x . For plutonium, the very formation of PuO 2+x has challenged a long-established dogma, and raised fundamental questions for long-term storage and environmental migration. This presentation covers two aspects of Los Alamos synchrotron radiation studies of plutonium oxides: (1) the structural chemistry of laboratory-prepared AnO 2+x systems (An = U, Pu; 0 ≤ x ≤ 0.25) determined through a combination of x-ray absorption fine structure spectroscopy (XAFS) and x-ray scattering of laboratory prepared samples; and (2) the application of synchrotron radiation towards the decontamination and decommissioning of the Rocky Flats Environmental Technology Site. Making the case for particle transport mechanisms as the basis of plutonium and americium mobility, rather than aqueous sorption-desorption processes, established a successful scientific basis for the dominance of physical transport processes by wind and water. The scientific basis was successful because it was in agreement with general theory on insolubility of PuO 2 in oxidation state IV, results of ultrafiltration analyses of field water/sediment samples, XAFS analyses of soil, sediment, and concrete samples, and was also in general agreement with on-site monitoring data. This understanding allowed Site contractors to rapidly move to application of soil erosion and sediment transport models as the means of predicting plutonium and americium transport, which led to design and application of site-wide soil erosion control technology to help control downstream concentrations of plutonium and americium in streamflow.

Assessment of microwave-based clinical waste decontamination unit.

Science.gov (United States)

Hoffman, P N; Hanley, M J

1994-12-01

A clinical waste decontamination unit that used microwave-generated heat was assessed for operator safety and efficacy. Tests with loads artificially contaminated with aerosol-forming particles showed that no particles were detected outside the machine provided the seals and covers were correctly seated. Thermometric measurement of a self-generated steam decontamination cycle was used to determine the parameters needed to ensure heat disinfection of the waste reception hopper, prior to entry for maintenance or repair. Bacterial and thermometric test pieces were passed through the machine within a full load of clinical waste. These test pieces, designed to represent a worst case situation, were enclosed in aluminium foil to shield them from direct microwave energy. None of the 100 bacterial test pieces yielded growth on culture and all 100 thermal test pieces achieved temperatures in excess of 99 degrees C during their passage through the decontamination unit. It was concluded that this method may be used to render safe the bulk of of ward-generated clinical waste.

Evaluation of a process for the decontamination of radioactive hotspots due to activated stellite particles

International Nuclear Information System (INIS)

Subramanian, V.; Chandramohan, P.; Srinivasan, M.P.; Rangarajan, S.; Velmurugan, S.; Narasimhan, S.V.; Khandelwal, R.C.

2010-01-01

Some of the Indian PHWRs which used stellite balls in the ball and screw mechanism of the adjustor rod drive mechanism in the moderator circuit encountered high radiation field in moderator system due to 60 Co. Release of particulate stellite was responsible for the hotspots besides the general uniform contamination of internal surfaces with 60 Co. Extensive laboratory studies have shown that it is possible to dissolve these stellite particles by adopting a three step redox process with permanganic acid as the oxidizing agent. These investigations with inactive stellite in powder form helped to optimize the process conditions. Permanganic acid was found to have the highest dissolution efficiency as compared to alkaline and nitric acid permanganate. The concentration of the permanganate was also found to be an important factor in deciding the efficiency of the dissolution of stellite. The efficiency of dissolution as a function of permanganic acid concentration showed a maximum. This process was evaluated for its effectiveness on components from nuclear power plants. Component decontamination was carried out on adjustor rod drive assemblies which had 60 Co activity due to stellite particles with the radiation field ranging from 3 R/h to 20 R/h. They were subjected to decontamination with permanganic acid as oxidizing agent, followed by citric acid and a solution containing EDTA, ascorbic acid and citric acid in 4:3:3 ratio by weight (EAC) as reducing formulations. A test rig was fabricated for this purpose. In the first trial, one adjustor rod drive mechanism was subjected to decontamination. After two cycles of treatment, an average decontamination factor (DF) of 6.8, with a maximum DF of 11.7 was achieved. The same process but one cycle was repeated on eight more adjustor rod drive mechanisms. 60 Co activity in the range of 13 - 93 mCi was removed from these adjustor rods. Loose contamination of the order of 30000 - 40000 dpm/cm 2 observed before decontamination

Low impact plutonium glovebox D&D

Energy Technology Data Exchange (ETDEWEB)

Rose, R.W.

1995-12-31

A dilemma often encountered in decontamination and decommissioning operations is the lack of choice as to the location where the work is to be performed. Facility siting, laboratory location, and adjacent support areas were often determined based on criteria, which while appropriate at the time, are not always the most conducive to a D&D project. One must learn to adapt and cope with as found conditions. High priority research activities, which cannot be interrupted, may be occurring in adjacent non-radiological facilities in the immediate vicinity where highly contaminated materials must be handled in the course of a D&D operation. The execution of a project within such an environment involves a high level of coordination, cooperation, professionalism and flexibility among the project, the work force and the surrounding occupants. Simply moving occupants from the potentially affected area is not always an option and much consideration must be given in the selection of the D&D methodology to be employed and the processes to be implemented. Determining project boundaries and the ensuring that adjacent occupants are included in the planning/scheduling of specific operations which impact their work area are important in the development of the safety envelope. Such was the case in the recent D&D of 61 gloveboxes contaminated with plutonium and other transuranic nuclides at the Argonne National Laboratory-East site. The gloveboxes, which were used in Department of Energy research and development program activities over the past 30 years, were decontaminated to below transuranic waste criteria, size reduced, packaged and removed from Building 212 by Argonne National Laboratory personnel in conjunction with Nuclear Fuel Services, Inc. with essentially no impact to adjacent occupants.

Development of the dry decontamination technique using plasma

Energy Technology Data Exchange (ETDEWEB)

Kim, Yong Soo; Seo, Yong Dae; Lee, Dong Uk; Jeon, Sang Hwan; Jung, Young Suk [Hanyang University, Seoul (Korea)

2001-04-01

In order to develop an advanced dry decontamination method, dry decontamination technique using gaseous plasma is studied. Scopes of the research are 1) literature survey and case studies of the international R and D activities and industrial application, 2) contaminant characteristics analysis, 3) feasibility and applicability study of the unit techniques, 4) process development study on the plasma decontamination, 5) plasma diagnostics and quantitative analysis by QMS and OES, and 6) design of (microwave) plasma torch system. The major research results are as belows. The maximum etching rate of UO{sub 2} is achieved to be 0.8 {mu}m/min. under 300 deg C, 150 W CF{sub 4}/O{sub 2}/N{sub 2} r.f. plasma maintaining the optimum ratio of CF{sub 4}/O{sub 2} of four, and that of Co and Mo is 0.06 {mu}m/min. and 1.9 {mu}m/min., respectively, under 380 deg C, 220 W CF{sub 4}/O{sub 2} r.f. plasma. The optimum process for the dry decontamination of TRU, CP, and or FP nuclides, therefore, requires the optimum gas composition above 350 deg C and 220W power. It is also demonstrated that this optimum process can be extrapolated to atmospheric high power torch system. In conclusion, if plasma power and temperature increases with maintaining the optimum gas composition, this dry decontamination techniques must be definitely effective and efficient. 17 refs., 62 figs., 4 tabs. (Author)

Comparison of skin decontamination efficacy of commercial decontamination products following exposure to VX on human skin.

Science.gov (United States)

Thors, L; Koch, M; Wigenstam, E; Koch, B; Hägglund, L; Bucht, A

2017-08-01

The decontamination efficacy of four commercially available skin decontamination products following exposure to the nerve agent VX was evaluated in vitro utilizing a diffusion cell and dermatomed human skin. The products included were Reactive Skin Decontamination Lotion (RSDL), the Swedish decontamination powder 104 (PS104), the absorbent Fuller's Earth and the aqueous solution alldecontMED. In addition, various decontamination procedures were assessed to further investigate important mechanisms involved in the specific products, e.g. decontamination removal from skin, physical removal by sponge swabbing and activation of degradation mechanisms. The efficacy of each decontamination product was evaluated 5 or 30 min after dermal application of VX (neat or diluted to 20% in water). The RSDL-lotion was superior in reducing the penetration of VX through human skin, both when exposed as neat agent and when diluted to 20% in water. Swabbing with the RSDL-sponge during 2 min revealed decreased efficacy compared to applying the RSDL-lotion directly on the skin for 30 min. Decontamination with Fuller's Earth and alldecontMED significantly reduced the penetration of neat concentration of VX through human skin. PS104-powder was insufficient for decontamination of VX at both time-points, independently of the skin contact time of PS104. The PS104-slurry (a mixture of PS104-powder and water), slightly improved the decontamination efficacy. Comparing the time-points for initiated decontamination revealed less penetrated VX for RSDL and Fuller's Earth when decontamination was initiated after 5 min compared to 30 min post-exposure, while alldecontMED displayed similar efficacy at both time-points. Decontamination by washing with water only resulted in a significant reduction of penetrated VX when washing was performed 5 min after exposure, but not when decontamination was delayed to 30 min post-exposure of neat VX. In conclusion, early initiated decontamination with the

Decontamination of radioactive isotopes

International Nuclear Information System (INIS)

Despotovic, R.; Music, S.; Subotic, B.; Wolf, R.H.H.

1979-01-01

Removal of radioactive isotopes under controlled conditions is determined by a number of physical and chemical properties considered radiocontaminating and by the characteristics of the contaminated object. Determination of quantitative and qualitative factors for equilibrium in a contamination-decontamination system provides the basis for rational and successful decontamination. The decontamination of various ''solid/liquid'' systems is interesting from the scientific and technological point of view. These systems are of great importance in radiation protection (decontamination of various surfaces, liquids, drinking water, fixation or collection of radiocontaminants). Different types of decontamination systems are discussed. The dependence of rate and efficiency of the preparation conditions and on the ageing of the scavenger is described. The influence of coagulating electrolyte on radioactive isotope fixation efficiency was also determined. The fixation of fission radionuclide on oxide scavengers has been studied. The connection between fundamental investigations and practical decontamination of the ''solid/liquid'' systems is discussed. (author)

Purpose and objectives for international plutonium storage

International Nuclear Information System (INIS)

Kupp, R.W.

1983-01-01

Separated and decontaminated plutonium - out of a reactor, in a bottle, tank or canister represents an easy target for diversion into possible non-peaceful uses. It also presents a situation that is of concern from a terrorist attack standpoint. Because this special nuclear material has such national and international sensitivity, storage for those quantities which are ''in excess'' of those necessary to be used for peaceful purposes is of concern to the Nations of the World. Recognizing these concerns, Article XII.A.5 of the IAEA Statutes was developed (1956) and the introduction to this Sub-article 5 states ''...that with respect to any Agency Project or other arrangements where the Agency is requested by the parties concerned to apply safeguards, the Agency shall have the following rights and responsibilities to the extent relevant to the project or arrangement....'' Article XII.A.5 then continues: ''To approve the means to be used for chemical processing.... to insure that this chemical processing will not lend itself to diversion of materials for military purposes.... to require that special additional materials recovered or produced as by-product be used for peaceful purposes under continuing Agency safeguards, for research or in reactors.... and to require deposit with the Agency of any excess.... over what is needed for the above stated uses in order to prevent stockpiling of these materials, provided that thereafter, at the request of the member or members concerned.... (plutonium) shall be returned promptly.... for use under the same provisions as stated above.''

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.)

LASL experience in decontamination of the environment

International Nuclear Information System (INIS)

Ahlquist, A.J.

1979-01-01

Since 1972 the Los Alamos Scientific Laboratory (LASL) has been actively involved in land area surveys for radioactive contamination and has gained considerable experience in cleanup of lands considered to have unacceptable levels of radioactive contamination. Experience and means of arriving at recommendations for decontamination at levels as low as reasonably achievable

Separations canyon decontamination facilities

International Nuclear Information System (INIS)

Hershey, J.H.

1975-01-01

Highly radioactive process equipment is decontaminated at the Savannah River Plant in specially equipped areas of the separations canyon building so that direct mechanical repairs or alterations can be made. Using these facilities it is possible to decontaminate and repair equipment such as 10- x 11-ft storage tanks, 8- x 8-ft batch evaporator pots and columns, 40-in. Bird centrifuges, canyon pumps and agitators, and various canyon piping systems or ''jumpers.'' For example, centrifuge or evaporator pots can be decontaminated and rebuilt for about 60 percent of the 1974 replacement cost. The combined facilities can decontaminate and repair 6 to 10 pieces of major equipment per year. Decontamination time varies with type of equipment and radioactivity levels encountered

Separations canyon decontamination facilities

International Nuclear Information System (INIS)

Hershey, J.H.

1975-05-01

Highly radioactive process equipment is decontaminated at the Savannah River Plant in specially equipped areas of the separations canyon buildings so that direct mechanical repairs or alterations can be made. Using these facilities it is possible to decontaminate and repair equipment such as 10- x 11-ft storage tanks, 8- x 8-ft batch evaporator pots and columns, 40-in. Bird centrifuges, canyon pumps and agitators, and various canyon piping systems or ''jumpers.'' For example, centrifuge or evaporator pots can be decontaminated and rebuilt for about 60 percent of the 1974 replacement cost. The combined facilities can decontaminate and repair 6 to 10 pieces of major equipment per year. Decontamination time varies with type of equipment and radioactivity levels encountered. (U.S.)

Development of chemical decontamination process with sulfuric acid-cerium (IV) for decommissioning

International Nuclear Information System (INIS)

Suwa, Takeshi; Kuribayashi, Nobuhide; Tachikawa, Enzo

1988-01-01

The electrolytic regeneration of Ce 4+ from Ce 3+ , which is required to achieve a high decontamination factor (DF) in this process, has been investigated. A calculating model was derived for the regenerating current required during the decontamination as a function of dissolution rate of crud, corrosion rate (R c ), current efficiency (η e ) and characteristics of decontamination loop. From the above calculation, it was found that the current was mainly governed by R c and η e . A condition to obtain a high DF at low R c and high η e has been found experimentally by use of a mixture of Ce 3+ at the ratio of Ce 4+ /Ce 3+ = 0.1 ∼ 0.2. The desired values to be η e ≥ 80 % at above 50 A/m 2 was obtained under the flow rate above 300 cm/min and Ce 3+ concentration above 10 x 10 -3 M at 60 deg C using the dual-cylindrical type cell. The current efficiency was also investigated with cells of various geometries. The present decontamination process has been proposed as a system decontamination process, which is essentially a single-step decontamination process for Cr-rich oxides. (author)

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)

Chemical decontamination method in nuclear facility system

International Nuclear Information System (INIS)

Takahashi, Ryota; Sakai, Hitoshi; Oka, Shigehiro.

1996-01-01

Pumps and valves in a closed recycling loop system incorporating materials to be chemically decontaminated are decomposed, a guide plate having the decomposed parts as an exit/inlet of a decontaminating liquid is formed, and a decontaminating liquid recycling loop comprising a recycling pump and a heater is connected to the guide plate. Decontaminating liquid from a decontaminating liquid storage tank is supplied to the decontaminating liquid recycling loop. With such constitutions, the decontaminating liquid is filled in the recycling closed loop system incorporating materials to be decontaminated, and the materials to be decontaminated are chemically decontaminated. The decontaminating liquid after the decontamination is discharged and flows, if necessary, in a recycling system channel for repeating supply and discharge. After the decontamination, the guide plate is removed and returned to the original recycling loop. When pipelines of a reactor recycling system are decontaminated, the amount of decontaminations can be decreased, and reforming construction for assembling the recycling loop again, which requires cutting for pipelines in the system is no more necessary. Accordingly, the amount of wastes can be decreased, and therefore, the decontamination operation is facilitated and radiation dose can be reduced. (T.M.)

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)

Decontamination of radioisotope production facility

International Nuclear Information System (INIS)

Daryoko, M.; Yatim, S.; Suseno, H.; Wiratmo, M.

1998-01-01

The strippable coating method use phosphoric glycerol and irradiated latex as supporting agents have been investigated. The investigation used some decontaminating agents: EDTA, citric acid, oxalic acid and potassium permanganate were combined with phosphoric glycerol supporting agent, then EDTA Na 2 , sodium citric, sodium oxalic and potassium permanganate were combined with irradiated latex supporting agent. The study was needed to obtain the representative operating data, will be implemented to decontamination the Hot Cell for radioisotope production. The experiment used 50x50x1 mm stainless steel samples and contaminated by Cs-137 about 1.1x10 -3 μCi/cm 2 . This samples according to inner cover of Hot Cell material, and Hot Cell activities. The decontamination factor results of the investigation were: phosphoric glycerol as supporting agent, about 20 (EDTA as decontaminating agent) to 47 (oxalic acid as decontaminating agent), and irradiated latex as supporting agent, about 11.5 (without decontamination agent) to 27 (KMnO 4 as decontaminating agent). All composition of the investigation have been obtained the good results, and can be implemented for decontamination of Hot Cell for radioisotope production. The irradiated latex could be recommended as supporting agent without decontaminating agent, because it is very easy to operate and very cheap cost. (author)

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...

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)

Decontamination of medical radioisotopes from hard surfaces using peelable polymer-based decontamination agents

International Nuclear Information System (INIS)

Draine, Amanda E.; Walter, Ken J.; Johnson, Thomas E.

2008-01-01

Full text: Medical radioisotopes used to treat and diagnose patients often contaminate surfaces in patient treatment rooms. They are typically short-lived and decay within a matter of days or weeks. However, down time in a medical facility related to radioisotope contamination is costly and can impact patient care. Most liquid or solid spills can be contained and disposed in radioactive wastes fairly completely and quickly; however residual contamination may remain on the contacted surface. Although liquid decontamination agents can be used to address the issue of residual contamination, they often require multiple applications with attendant scrubbing and wiping. Liquid decontamination can also produce large volumes of low-level radioactive waste. To look at reducing radioactive waste volumes, research was conducted on the efficacy of three low-volume peel able decontamination agents. Testing was performed on hard surfaces, such as vinyl composition floor tiles and stainless steel, which are found in many hospitals, research laboratories, and universities. The tiles were contaminated with the medical use isotopes of 99m Tc, Tl-201, and I-131 and subsequently decontaminated with one of the three decontamination agents. Quantitative and qualitative data were obtained for each of three different peel able decontamination agent formulations. Quantitative data included environmental temperature and relative humidity, application thickness, dry time, contact time, and decontamination efficacy of the agents on the tested surfaces. Qualitative factors included ease of application and pee lability, as well as sag resistance and odor of each agent. Initial studies showed that under standard conditions there were reproducible differences in the decontamination efficacies among the three different decontamination formulations. (author)

Bioinspired Surface Treatments for Improved Decontamination: Handling andDecontamination Considerations

Science.gov (United States)

2018-03-16

and Decontamination Considerations Brandy J. White Martin H. Moore Brian J. Melde Laboratory for the Study of Molecular Interfacial Interactions...Decontamination Considerations Brandy J. White, Martin H. Moore, Brian J. Melde, Anthony P. Malanoksi, and Chanté Campbell1 Center for Bio/Molecular

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

International Nuclear Information System (INIS)

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

1996-01-01

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

Development of Nuclear Decontamination Technology Using Supercritical Fluid

Energy Technology Data Exchange (ETDEWEB)

Jung, Wonyoung; Park, Kwangheon; Park, Jihye; Lee, Donghee [Kyunghee Univ., Yongin (Korea, Republic of)

2014-05-15

Soil cleaning technologies that have been developed thus far increase treatment costs in contaminated soil recovery processes because they generate large amounts of secondary wastes. In this respect, this study is intended to develop soil decontamination methods using CO{sub 2}, which is a nontoxic, environmentally friendly substance, in order to fundamentally suppress the generation of secondary wastes from the decontamination process and to create high added values. In this study, to develop decontamination methods for uranium-contaminated soil using supercritical CO{sub 2}, a soil decontamination system using supercritical CO{sub 2} was constructed. In addition, the basic principle of supercritical CO{sub 2} decontamination using a TBP-HNO3 complex was explained. According to the results of the study, sea-sand samples having the same degree of contamination showed different results of decontamination according to the quantities of the TBP-HNO3 complex used as an extraction agent, which resulted in high extraction rates. Thus far, a most widely used method of extracting uranium has been the dissolving of uranium in acids. However, this method has the large adverse effect of generating strong acidic wastes that cannot be easily treated. On the other hand, supercritical CO{sub 2} requires critical conditions that are no more difficult to meet than those of other supercritical fluids, since its density can be changed from a very low state close to that of an ideal gas to a high state close to that of liquids. The critical gas conditions are a pressure of 71 bar and a temperature of 31 .deg. C, both of which are inexpensive to achieve. Moreover, CO{sub 2} is a solvent that is not harmful to the human body and few effects on environmental pollution. Therefore, nontoxic and environment friendly processes can be developed using supercritical CO{sub 2}. Supercritical CO{sub 2}'s advantages over prevailing methods suggest its potential for developing innovative

Development of Nuclear Decontamination Technology Using Supercritical Fluid

International Nuclear Information System (INIS)

Jung, Wonyoung; Park, Kwangheon; Park, Jihye; Lee, Donghee

2014-01-01

Soil cleaning technologies that have been developed thus far increase treatment costs in contaminated soil recovery processes because they generate large amounts of secondary wastes. In this respect, this study is intended to develop soil decontamination methods using CO 2 , which is a nontoxic, environmentally friendly substance, in order to fundamentally suppress the generation of secondary wastes from the decontamination process and to create high added values. In this study, to develop decontamination methods for uranium-contaminated soil using supercritical CO 2 , a soil decontamination system using supercritical CO 2 was constructed. In addition, the basic principle of supercritical CO 2 decontamination using a TBP-HNO3 complex was explained. According to the results of the study, sea-sand samples having the same degree of contamination showed different results of decontamination according to the quantities of the TBP-HNO3 complex used as an extraction agent, which resulted in high extraction rates. Thus far, a most widely used method of extracting uranium has been the dissolving of uranium in acids. However, this method has the large adverse effect of generating strong acidic wastes that cannot be easily treated. On the other hand, supercritical CO 2 requires critical conditions that are no more difficult to meet than those of other supercritical fluids, since its density can be changed from a very low state close to that of an ideal gas to a high state close to that of liquids. The critical gas conditions are a pressure of 71 bar and a temperature of 31 .deg. C, both of which are inexpensive to achieve. Moreover, CO 2 is a solvent that is not harmful to the human body and few effects on environmental pollution. Therefore, nontoxic and environment friendly processes can be developed using supercritical CO 2 . Supercritical CO 2 's advantages over prevailing methods suggest its potential for developing innovative decontamination methods, as demonstrated

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.

Overview of nonchemical decontamination techniques

International Nuclear Information System (INIS)

Allen, R.P.

1984-09-01

The decontamination techniques summarized in this paper represent a variety of surface cleaning methods developed or adapted for component and facility-type decontamination applications ranging from small hand tools to reactor cavities and other large surface areas. The major conclusion is that decontamination is a complex, demanding technical discipline. It requires knowledgeable, experienced and well-trained personnel to select proper techniques and combinations of techniques for the varied plant applications and to realize their full performance potential. Unfortunately, decontamination in many plants has the lowest priority of almost any activity. Operators are unskilled and turnover is so frequent that expensive decontamination capabilities remain unused while decontamination operations revert to the most rudimentary type of hand scrubbing and water spray cleaning

Exploiting the plutonium stockpiles in PWRs by using inert matrix fuel

International Nuclear Information System (INIS)

Lombardi, C.; Mazzola, A.

1996-01-01

The plutonium coming from dismantled warheads and that already stockpiled coming from spent fuel reprocessing have raised many concerns related to proliferation resistance, environmental safety and economy. The option of disposing of plutonium by fission is one of the most widely discussed and many proposals for plutonium burning in a safe and economical manner have been put forward. Due to their diffusion, PWRs appear to be the main candidates for the reduction of the plutonium stockpiles. In order to achieve a high plutonium consumption rate, a uranium-free fuel may be conceived, based on the dilution of PuO 2 within a carrier matrix made of inert oxide. In this paper, a partial loading of inert matrix fuel in a current technology PWR was investigated with 3-D calculations. The results indicated that this solution has good plutonium elimination capabilities: commercial PWRs operating in a once-through cycle scheme can transmute more than 98% of the loaded Pu-239 and 73 or 81% of the overall initially loaded reactor grade or weapons grade plutonium, respectively. The plutonium still let in the spent fuel was of poor quality and then offered a better proliferation resistance. Power peaking problems could be faced with the adoption of burnable absorbers: IFBA seemed to be particularly suitable. In spite of a reduction of the overall plutonium loaded mass by a factor 3.7 or 5.4 depending on its quality, there was no evidence of an increase of the minor actinides radiotoxicity after a time period of about 25 years. (author)

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.

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.)

324 and 325 Building hot cell cleanout program: Decontamination of C-Cell

International Nuclear Information System (INIS)

Katayama, Y.B.; Holton, L.K. Jr.

1989-10-01

During FY 1989 the decontamination of C-Cell of Hanford's 324 Building was completed as part of the 324 and 325 Building Hot Cell Cleanout Program sponsored by the DOE Nuclear Energy's Surplus Facilities Management Program. The decontamination effort was completed using a series of remote and contact decontamination techniques. Initial radiation readings in C-Cell averaged 50 rad/hr and were reduced remotely to less than 200 mrad/hr using an alkaline foam cleaner followed by a 5000-psi water flush. Contact decontamination was then permissible using ultra high-pressure water, at 36,000 psi, further reducing the average radiation level in the cell to less than 86 mrem/hr. The approach used in decontaminating C-Cell resulted in a savings in radiation exposure of 87% and a cost savings of 39% compared to a hands-on procedure used in A-Cell, 324 Building in 1987. The radiation dose and the costs to achieve a 244-fold reduction in radiation contamination were 1.65 mrem per ft 2 and $96 per ft 2 of cell surface area. 14 figs., 4 tabs

Method for decontaminating radiation metal waste

International Nuclear Information System (INIS)

Onuma, Tsutomu; Tanaka, Akio; Akimoto, Hidetoshi

1991-01-01

This report describes a method for decontaminating radiation metal waste characterized by the following properties: in order to decontaminate radiation metal waste of various shapes produced by facilities involved with radioactive substances, non-complex shapes are decontaminated by electropolishing the materials in a neutral saline solution. Complex shapes are chemically decontaminated by means of an acid solution containing permanganic acid or an alkaline solution and a mineral acid solution. After neutralizing the solutions used for chemical decontamination, the radioactive material is separated and removed. Further, in the decontamination method for radioactive metal waste, a supernatant liquid is reused as the electrolyte in electropolishing decontamination. Permanganic ions (MnO 4 - ) are reduced to manganese dioxide (MnO 2 ) and deposited prior to neutralizing the solution used for chemical decontamination. Once manganese dioxide (MnO 2 ) has been separated and removed, it is re-used as the electrolyte in electropolishing decontamination by means of a process identical to the separation process for radioactive substances. 3 figs

Decontamination of the RA reactor heavy water system, Annex 9

International Nuclear Information System (INIS)

Maksimovic, Z.B.; Nikolic, R.M.; Marinkovic, M.D.; Jelic, Lj.M.

1963-01-01

Both stainless steel and aluminium parts of the RA reactor heavy water system system were decontaminated as well as the heavy water itself. System was contaminated with 60 Co. Decontamination factor was determined by activity measurements during distillation. Concentration of the corrosion products in the heavy water was measured by spectrochemical analysis, and found to be 0.1 - 1 mg/l. Chemical analyses of the aluminium and stainless steel surfaces showed that cobalt was adsorbed on the aluminium oxide layer. Water solution of 7%H 3 PO 4 + 2% CrO 3 was used for decontamination of the heavy water system and distillation device. This was found to be the most efficient solvent which does not affect stainless steel corrosion. Decontamination factors achieved were from 60 - 100. Decontamination results enabled determining the distribution of cobalt in the system: 10 Ci on the stainless steel parts, 50 Ci in the heavy water; and above 600 Ci on the fuel and experimental channels. Specific activity of 60 Co was calculated to be 15 Ci/g on the reactor channels, 8 Ci/g on the stainless steel parts and 3 Ci/g in the heavy water. Decontamination of the aluminium parts was not done because it was considered it could initiate corrosion. Since the efficiency of distillation is increased it was expected that permanent distillation would remove most of the activity in the reactor channels

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.)

Solvent extraction process development for high plutonium fuel cycles

Energy Technology Data Exchange (ETDEWEB)

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

1994-06-01

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

Development of decontamination technology for the decommissioned Bohunice A-1 nuclear power plant

International Nuclear Information System (INIS)

Krejci, F.; Majersky, D.; Solcanyi, M.; Sekely, S.; Kucharik, D.

1991-01-01

The main results of investigation into the decontamination technology for the equipment and buildings of the decommissioned A-1 nuclear power plant, achieved by the Nuclear Power Plants Research Institute in Trnava over the 1988-1990 period, are summarized. Mobile decontamination and recirculation equipment has been developed for pre-disassembling decontamination. A solution containing formic acid (19 g/l), EDTA-Na 4 (6 g/l) and thiourea (0.5 g/l) was used for decontamination of low-alloy steels; for materials from the steam generators and turbo-compressors, the decontamination factor (DF) of this solution was 30 to 150 per decontamination cycle. For high-alloy steels, a two-stage process comprising the use of an oxidation solution and a reduction solution appeared suitable. The oxidation solution contained potassium permanganate (0.6 g/l) and nitric acid (0.4 g/l), whereas the reduction solution, viz. Citrox 21, contained citric acid (0.5 g/l), oxalic acid (1.0 g/l) and EDTA-NA 4 (2.5 g/l). The DF is 10 to 50 in one oxidation-reduction cycle and 50-100 in two cycles. For the post-disassembling chemical decontamination, the contaminated material was cut into pieces 70 to 80 cm long, freed from grease and decontaminated chemically by submerging in the solution while applying treatment by ultrasound. A technology of electrochemical decontamination has also been developed. It appeared particularly suitable for structural materials of the primary coolant circuit comprising austenitic stainless steels and low-alloy steels after pre-disassembling chemical decontamination with remainders of the corrosion layer, and for structural materials of the secondary coolant circuit after chemical post-disassembling decontamination. Research in the field of decontamination of the building parts and of the outer surfaces of the structural materials concentrated mainly on the use of decontamination foams. Foaming solutions have been developed for the decontamination of PESL floors and

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)

Verification of wet blasting decontamination technology

International Nuclear Information System (INIS)

Matsubara, Sachito; Murayama, Kazunari; Yoshida, Hirohisa; Igei, Shigemitsu; Izumida, Tatsuo

2013-01-01

Macoho Co., Ltd. participated in the projects of 'Decontamination Verification Test FY 2011 by the Ministry of the Environment' and 'Decontamination Verification Test FY 2011 by the Cabinet Office.' And we tested verification to use a wet blasting technology for decontamination of rubble and roads contaminated by the accident of Fukushima Daiichi Nuclear Power Plant of the Tokyo Electric Power Company. As a results of the verification test, the wet blasting decontamination technology showed that a decontamination rate became 60-80% for concrete paving, interlocking, dense-grated asphalt pavement when applied to the decontamination of the road. When it was applied to rubble decontamination, a decontamination rate was 50-60% for gravel and approximately 90% for concrete and wood. It was thought that Cs-134 and Cs-137 attached to the fine sludge scraped off from a decontamination object and the sludge was found to be separated from abrasives by wet cyclene classification: the activity concentration of the abrasives is 1/30 or less than the sludge. The result shows that the abrasives can be reused without problems when the wet blasting decontamination technology is used. (author)

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.

Irradiation as an alternative environment friendly method for microbiological decontamination of herbal raw material

International Nuclear Information System (INIS)

Gorecki, P.; Kedzia, B.; Migdal, W.; Owczarczyk, H.B.

1998-01-01

Microbiological contamination of herbal raw materials is a serious problem in the production of therapeutical preparations. A good quality of the product, according to the pharmaceutical requirements may be achieved by applying suitable methods of decontamination. The decontamination treatments should be fast and effective against all microorganisms. It should ensure the decontamination of both packaging and the product in order to act effectively against all the microorganisms present and must not reduce the sensory and technological qualities of the commodities. In the paper, the results of comparative investigations on the microbiological decontamination of herbal raw materials by chemical (ethylene oxide, methyl bromide) and physical method (irradiation) are presented. Decontamination of herbal raw materials by irradiation is a method by choice. It is because chemical methods have been recognized recently as not safe to the consumer. Irradiation, in turn, is technically feasible, very effective and friendly enough to environment process

New decontamination technologies for environmental applications

International Nuclear Information System (INIS)

Allen, R.P.; Arrowsmith, H.W.; McCoy, M.W.

1981-01-01

The technologies discussed represent a versatile collection of tools and approaches for environmental decontamination applications. The fixatives provide a means for gaining and maintaining control of large contaminated areas, for decontaminating large surface areas, and for protecting equipment and supplies used in decontamination operations. The other decontamination techniques together provide a method for removing loose surface contamination from almost all classes of materials and surfaces. These techniques should have wide application both as direct decontamination processes and for the cleaning of tools and equipment used in the decontamination operations

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.

Isotopic analysis of plutonium by computer controlled mass spectrometry

International Nuclear Information System (INIS)

1974-01-01

Isotopic analysis of plutonium chemically purified by ion exchange is achieved using a thermal ionization mass spectrometer. Data acquisition from and control of the instrument is done automatically with a dedicated system computer in real time with subsequent automatic data reduction and reporting. Separation of isotopes is achieved by varying the ion accelerating high voltage with accurate computer control

Non-destructive decontamination of building materials

Science.gov (United States)

Holecek, Josef; Otahal, Petr

2015-11-01

For nondestructive radiation decontamination of surfaces it is necessary to use varnishes, such as ARGONNE, DG1101, DG1108, etc. This text evaluates the use of manufactured strippable coatings for radiation decontamination. To evaluate decontamination capability of such coatings the following varnishes were selected and subsequently used: AZ 1-700 and AXAL 1807S. The varnishes were tested on different building materials surfaces contaminated by short-term radioisotopes of Na-24 or La-140, in water soluble or water insoluble forms. Decontamination quality was assessed by the decontamination efficiency value, defined as the proportion of removed activity to the applied activity. It was found that decontamination efficiency of both used varnishes depends not only on the form of contaminant, but in the case of application of AXAL 1807S varnish it also depends on the method of its application on the contaminated surface. The values of the decontamination efficiency for AZ1-700 varnish range from 46% for decontamination of a soluble form of the radioisotope from concrete surface to 98% for the decontamination of a soluble form of the radioisotope from ceramic tile surface. The decontamination efficiency values determined for AXAL 1807S varnish range from 48% for decontamination of a soluble form of the radioisotope from concrete surface to 96% for decontamination of an insoluble form of the radioisotope from ceramic tile surface. Comparing these values to the values given for the decontaminating varnishes we can conclude that AXAL 1807S varnish is possible to use on all materials, except highly porous materials, such as plasterboard or breeze blocks, or plastic materials. AZ 1-700 varnish can be used for all dry materials except plasterboard.

Thermal decontamination of transformers: A new technology

International Nuclear Information System (INIS)

Colak, P.Z.

1992-01-01

After evaluating a number of methods for decontaminating or disposing of transformers that contained polychlorinated biphenyls (PCB), it was concluded that no entirely satisfactory procedure or technology was yet available which was permanent, effective, safe, relatively simple, and based on proven technology or conventional practice. The most desirable compromise appears to be thermal decontamination. It is proposed to decontaminate transformers by controlled incineration in a specially designed, indirect-fired furnace which resembles the conventional bell-type, vertical elevator, metal heat treating type of furnace. The design differs in the incorporation of those essential features required to achieve oxidation of the organic components, to provide internal air circulation needed to ensure efficient heat and mass transfer, and other factors. The most appropriate decontamination facility would provide for implementation of the following procedures: draining of PCB-containing liquids from the transformer; limited disassembly of the transformer, which in most instances would imply only removal of the top cover to expose the insides; and controlled incineration with any vapors generated being conducted to a secondary combustion chamber. Experiments were conducted in a kiln to simulate the proposed transformer incinerator. Results show that exposure of the transformer segments to a temperature in the 950-1,000 degree C range for over 90 min is generally sufficient to reduce the PCB content to under 1 ppM. Based on the work conducted, a suitable bell furnace was constructed and added to the Swan Hills (Alberta) waste treatment facility. 2 figs., 3 tabs

Large-bore pipe decontamination

International Nuclear Information System (INIS)

Ebadian, M.A.

1998-01-01

The decontamination and decommissioning (D and D) of 1200 buildings within the US Department of Energy-Office of Environmental Management (DOE-EM) Complex will require the disposition of miles of pipe. The disposition of large-bore pipe, in particular, presents difficulties in the area of decontamination and characterization. The pipe is potentially contaminated internally as well as externally. This situation requires a system capable of decontaminating and characterizing both the inside and outside of the pipe. Current decontamination and characterization systems are not designed for application to this geometry, making the direct disposal of piping systems necessary in many cases. The pipe often creates voids in the disposal cell, which requires the pipe to be cut in half or filled with a grout material. These methods are labor intensive and costly to perform on large volumes of pipe. Direct disposal does not take advantage of recycling, which could provide monetary dividends. To facilitate the decontamination and characterization of large-bore piping and thereby reduce the volume of piping required for disposal, a detailed analysis will be conducted to document the pipe remediation problem set; determine potential technologies to solve this remediation problem set; design and laboratory test potential decontamination and characterization technologies; fabricate a prototype system; provide a cost-benefit analysis of the proposed system; and transfer the technology to industry. This report summarizes the activities performed during fiscal year 1997 and describes the planned activities for fiscal year 1998. Accomplishments for FY97 include the development of the applicable and relevant and appropriate regulations, the screening of decontamination and characterization technologies, and the selection and initial design of the decontamination system

Optimization and plutonium equilibrium

International Nuclear Information System (INIS)

Silver, G.L.

1976-01-01

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

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

International Nuclear Information System (INIS)

Gutierrez Martinez, E.A.

1998-02-01

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

Evaluation of a process for the decontamination of radioactive hotspots due to activated stellite particles

Energy Technology Data Exchange (ETDEWEB)

Subramanian, V.; Chandramohan, P.; Srinivasan, M.P.; Rangarajan, S.; Velmurugan, S.; Narasimhan, S.V., E-mail: svn@igcar.gov.in [BARC Facilities, Water and Steam Chemistry Div., Kalpakkam, Tamilnadu (India); Khandelwal, R.C. [Kakrapara Atomic Power Station, KAPS, Surat, Gujarat (India)

2010-07-01

Some of the Indian PHWRs which used stellite balls in the ball and screw mechanism of the adjustor rod drive mechanism in the moderator circuit encountered high radiation field in moderator system due to {sup 60}Co. Release of particulate stellite was responsible for the hotspots besides the general uniform contamination of internal surfaces with {sup 60}Co. Extensive laboratory studies have shown that it is possible to dissolve these stellite particles by adopting a three step redox process with permanganic acid as the oxidizing agent. These investigations with inactive stellite in powder form helped to optimize the process conditions. Permanganic acid was found to have the highest dissolution efficiency as compared to alkaline and nitric acid permanganate. The concentration of the permanganate was also found to be an important factor in deciding the efficiency of the dissolution of stellite. The efficiency of dissolution as a function of permanganic acid concentration showed a maximum. This process was evaluated for its effectiveness on components from nuclear power plants. Component decontamination was carried out on adjustor rod drive assemblies which had {sup 60}Co activity due to stellite particles with the radiation field ranging from 3 R/h to 20 R/h. They were subjected to decontamination with permanganic acid as oxidizing agent, followed by citric acid and a solution containing EDTA, ascorbic acid and citric acid in 4:3:3 ratio by weight (EAC) as reducing formulations. A test rig was fabricated for this purpose. In the first trial, one adjustor rod drive mechanism was subjected to decontamination. After two cycles of treatment, an average decontamination factor (DF) of 6.8, with a maximum DF of 11.7 was achieved. The same process but one cycle was repeated on eight more adjustor rod drive mechanisms. {sup 60}Co activity in the range of 13 - 93 mCi was removed from these adjustor rods. Loose contamination of the order of 30000 - 40000 dpm/cm{sup 2} observed

Denatured plutonium: a study of deterrent action. Final report

International Nuclear Information System (INIS)

Hutchins, B.A.

1975-07-01

The safeguarding of nuclear reactor fuel includes physical security methods as well as technological process options. The purpose of this study was to provide a preliminary evaluation of a technological option; the introduction of denaturing as a deterrent to illicit plutonium diversion. Denaturing is accomplished by coextracting some highly-radioactive fission products with the plutonium during reprocessing of spent fuel. The radioactive denaturant is always in companion with the plutonium through all subsequent fuel cycle steps - and serves as a deterrent to diversion or illicit usage of this fissile source. In concept the denaturing approach is simple and straightforward. This report provides a preliminary analysis of denaturing which can be achieved within the framework of present reprocessing technology. The impact of denaturing is indicated by comparison to a conventional (i.e., non-denatured) light water reacter cycle approach

Decontamination processes for waste glass canisters

International Nuclear Information System (INIS)

Rankin, W.N.

1981-06-01

The process which will be used to decontaminate waste glass canisters at the Savannah River Plant consists of: decontamination (slurry blasting); rinse (high-pressure water); and spot decontamination (high-pressure water plus slurry). No additional waste will be produced by this process because glass frit used in decontamination will be mixed with the radioactive waste and fed into the glass melter. Decontamination of waste glass canisters with chemical and abrasive blasting techniques was investigated. The ability of a chemical technique with HNO 3 -HF and H 2 C 2 O 4 to remove baked-on contamination was demonstrated. A correlation between oxide removal and decontamination was observed. Oxide removal and, thus, decontamination by abrasive blasting techniques with glass frit as the abrasive was proposed and demonstrated

Decontamination processes for waste glass canisters

International Nuclear Information System (INIS)

Rankin, W.N.

1981-01-01

The process which will be used to decontaminate waste glass canisters at the Savannah River Plant consists of: decontamination (slurry blasting); rinse (high-pressure water); and spot decontamination (high-pressure water plus slurry). No additional waste will be produced by this process because glass frit used in decontamination will be mixed with the radioactive waste and fed into the glass melter. Decontamination of waste glass canisters with chemical and abrasive blasting techniques was investigated. The ability of a chemical technique with HNO 3 -HF and H 2 C 2 O 4 to remove baked-on contamination was demonstrated. A correlation between oxide removal and decontamination was observed. Oxide removal and, thus, decontamination by abrasive blasting techniques with glass frit as the abrasive was proposed and demonstrated

Plutonium roundtable discussion

International Nuclear Information System (INIS)

Penneman, R.A.

1982-01-01

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

Determination of the clean 4f peak shape in XPS for plutonium metal

Energy Technology Data Exchange (ETDEWEB)

Morrall, P. [AWE, Aldermaston, Reading, Berkshire RG7 4PR (United Kingdom)], E-mail: peter.morrall@awe.co.uk; Roussel, P. [AWE, Aldermaston, Reading, Berkshire RG7 4PR (United Kingdom); Jolly, L.; Brevet, A.; Delaunay, F. [Commissariat a l' Energie Atomique, Centre de Valduc, 21120 Is-sur-Tille (France)

2009-03-15

Many of the interesting properties observed with plutonium are ascribed to the influence of 5f electrons, and to the degree of localisation observed within these electrons. Indeed, changes in 5f localisation are sensitively reflected in the final states observed in core-level photoemission measurements. However, when analysing the 4f manifold of elemental plutonium, it is essential to obtain spectra without the influence of oxidation, which can easily be misinterpreted as 5f localisation. The ideal method to extract elemental plutonium 4f spectra is to remove any influence of oxidation from the 'clean' plutonium data by careful measurement of the oxygen 1s region, and the subsequent subtraction of the unwanted oxide features. However, in order to achieve this objective it is essential to determine the relative sensitivity factor (RSF) for plutonium 4f and the precise shape of the 4f features from plutonium sesqui-oxide. In this paper, we report an experimental determination of the RSF for the plutonium 4f manifold using experimental data captured from two different Vacuum Generators spectrometers; an ESCALAB Mk II and an ESCALAB 220i.

Summary of the Hanford Site decontamination, decommissioning, and cleanup, FY 1974--FY 1990

International Nuclear Information System (INIS)

Wahlen, R.K.

1991-08-01

At the end of World War II, the demand for more production along with process and military surveillance changes at the Hanford Site caused a continuing cycle of building and obsolescence. This trend continued until 1964, when the cutback in plutonium production began. The cutback caused the shutdown of excess production facilities. The last of eight reactors was shut down in 1971. Since that time, N Reactor has been the only production reactor that has operated. In addition, changes in the method of separating plutonium caused a number of excess facilities in the 200 Areas. Before 1973, no structured program existed for the disposal of unusable facilities or for general cleanup. Following a plant-wide safety and housekeeping inspection in 1973, a program was developed for the disposal of all surplus facilities. Since the start of FY 1974, a total of 46 radioactively contaminated sites have been demolished and disposed of. In addition, 28 buildings have been decontaminated for in situ disposal or for reuse, 21 contaminated sites have been stabilized, 131 clean structures have been removed, and 93 clean sites have received special remedial action to eliminate potential safety and/or environmental hazards. This report summarizes these activities. 3 refs, 1 fig., 18 tabs

Dwell time considerations for large area cold plasma decontamination

Science.gov (United States)

Konesky, Gregory

2009-05-01

Atmospheric discharge cold plasmas have been shown to be effective in the reduction of pathogenic bacteria and spores and in the decontamination of simulated chemical warfare agents, without the generation of toxic or harmful by-products. Cold plasmas may also be useful in assisting cleanup of radiological "dirty bombs." For practical applications in realistic scenarios, the plasma applicator must have both a large area of coverage, and a reasonably short dwell time. However, the literature contains a wide range of reported dwell times, from a few seconds to several minutes, needed to achieve a given level of reduction. This is largely due to different experimental conditions, and especially, different methods of generating the decontaminating plasma. We consider these different approaches and attempt to draw equivalencies among them, and use this to develop requirements for a practical, field-deployable plasma decontamination system. A plasma applicator with 12 square inches area and integral high voltage, high frequency generator is described.

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

Chemical decontaminating method for stainless steel

International Nuclear Information System (INIS)

Onuma, Tsutomu; Akimoto, Hidetoshi.

1990-01-01

Radioactive metal wastes comprising passivated stainless steels are chemically decontaminated to such a radioactivity level as that of usual wastes. The present invention for chemically decontaminating stainless steels comprises a first step of immersing decontaminates into a sulfuric acid solution and a second step of immersing them into an aqueous solution prepared by adding oxidative metal salts to sulfuric acid, in which a portion of the surface of stainless steels as decontaminates are chemically ground to partially expose substrate materials and then the above-mentioned decontamination steps are applied. More than 90% of radioactive materials are removed in this method by the dissolution of the exposed substrate materials and peeling of cruds secured to the surface of the materials upon dissolution. This method is applicable to decontamination of articles having complicate shapes, can reduce the amount of secondary wastes after decontamination and also remarkably shorten the time required for decontamination. (T.M.)

The large scale use of strippable coatings in preventative, tie-down and decontamination applications

International Nuclear Information System (INIS)

Sanders, M.J.; Pengelly, M.G.A.

1985-05-01

The use of strippable coatings both to remove and prevent the radioactive contamination of equipment is discussed. Details of application by brush, roller, conventional (air) and airless spray are given. The use of strippable coatings to prevent the components of a re-useable temporary containment system from becoming contaminated is described and results of simple tests in which the coatings were used to remove plutonium dioxide contamination from a number of different surfaces in a Pressurised Suit Area are given. It is concluded that strippable coatings are particularly useful in contamination prevention and tie-down roles but test results indicate that they do not possess overwhelming advantages when used as a decontamination technique. The products used in the work reported here are water based. (author)

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)

The Challenges of Preserving Historic Resources During the Deactivation and Decommissioning of Highly Contaminated Historically Significant Plutonium Process Facilities

International Nuclear Information System (INIS)

Hopkins, A.; Minette, M.; Sorenson, D.; Heineman, R.; Gerber, M.; Charboneau, S.; Bond, F.

2006-01-01

The Manhattan Project was initiated to develop nuclear weapons for use in World War II. The Hanford Engineer Works (HEW) was established in eastern Washington State as a production complex for the Manhattan Project. A major product of the HEW was plutonium. The buildings and process equipment used in the early phases of nuclear weapons development are historically significant because of the new and unique work that was performed. When environmental cleanup became Hanford's central mission in 1991, the Department of Energy (DOE) prepared for the deactivation and decommissioning of many of the old process facilities. In many cases, the process facilities were so contaminated, they faced demolition. The National Historic Preservation Act (NHPA) requires federal agencies to evaluate the historic significance of properties under their jurisdiction for eligibility for inclusion in the National Register of Historic Places before altering or demolishing them so that mitigation through documentation of the properties can occur. Specifically, federal agencies are required to evaluate their proposed actions against the effect the actions may have on districts, sites, buildings or structures that are included or eligible for inclusion in the National Register. In an agreement between the DOE's Richland Operations Office (RL), the Washington State Historic Preservation Office (SHPO) and the Advisory Council on Historic Preservation (ACHP), the agencies concurred that the Hanford Site Historic District is eligible for listing on the National Register of Historic Places and that a Site-wide Treatment Plan would streamline compliance with the NHPA while allowing RL to manage the cleanup of the Hanford Site. Currently, many of the old processing buildings at the Plutonium Finishing Plant (PFP) are undergoing deactivation and decommissioning. RL and Fluor Hanford project managers at the PFP are committed to preserving historical artifacts of the plutonium production process. They

Gentilly 1: decontamination program

International Nuclear Information System (INIS)

Le, H.; Denault, P.

1985-01-01

The Gentilly 1 station, a 250-MW(e) light-water-cooled and heavy-water-moderated nuclear reactor, is being decommissioned to a static state (variant of stage 1) condition by Atomic Energy of Canada Limited (AECL). The scope of the decontamination program at the Gentilly 1 site includes the fuel pool and associated systems, the decontamination center, the laundry, the feedwater pumps and piping systems, the service building ventilation and drainage systems, and miscellaneous floor and wall areas. After an extensive literature review for acceptable decontamination methods, it was decided that the decontamination equipment used at Gentilly 1 during the program would include a hydrolaser, a scarifier, chipping hammers, a steam cleaner, an ultrasonic bath, and cutting tools. In addition, various foams, acids, detergents, surfactants, and abrasives are used alone and in tandem with the above equipment. This paper highlights the result of these decontaminations, their effectiveness, and the recommendation for future application. The methodology in performing these operations are also presented

Disposition of plutonium from dismantled nuclear weapons: Fission options and comparisons

International Nuclear Information System (INIS)

Omberg, R.P.; Walter, C.E.

1993-01-01

Over the next decade, the United States expects to recover about 50 Mg of excess weapon plutonium and the Republic of Russia expects to recover a similar amount. Ensuring that these large quantities of high-grade material are not reused in nuclear weapons has drawn considerable attention. In response to this problem, the US Department of Energy (DOE) chartered the Plutonium Disposition Task Force (PDTF), in the summer of 1992, to assess a range of practical means for disposition of excess US plutonium. This report summarizes and compares the ''Fission Options'' provided to the Fission Working Group Review Committee (the committee) of the PDTF. The review by the committee was based on preliminary information received as of December 4, 1992, and as such the results summarized in this report should also be considered preliminary. The committee concluded that irradiation of excess weapon plutonium in fission reactors in conjunction with the generation of electricity and storing the spent fuel is a fast, cost-effective, and environmentally acceptable method of addressing the safeguards (diversion) issue. When applied appropriately, this method is consistent with current nonproliferation policy. The principal effect of implementing the fission options is at most a moderate addition of plutonium to that existing in commercial spent fuel. The amount of plutonium in commercial spent fuel by the year 2000 is estimated to be 300 Mg. The addition of 50 Mg of excess weapon plutonium, in this context, is not a determining factor, moreover, several of the fission options achieve substantial annihilation of plutonium

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

Decontaminating products for routine decontamination in nuclear power plants

International Nuclear Information System (INIS)

Henning, K.

2001-01-01

Routine decontamination work that has to be carried out in practical operation includes the cleaning of all kinds of surfaces such as floors, walls and apparatus, the decontamination of professional clothes and of the personnel. In order to ensure a trouble-free functioning of plants for the treatment of waste water and concentrate in nuclear power plants, radioactive liquid wastes appearing in the controlled area should be compatible with the treatment methods in practice. Radioactive concentrates and resides obtained from the treatment methods are mixed with matrix materials like cement or bitumen or treated by roller frame drying and thus are conditioned for intermediate or final storage. Several requirements should be made on decontaminating agents used in the controlled area. Some of these physical-chemical criteria will be described in detail. (R.P.)

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

Recommendations for skin decontamination

International Nuclear Information System (INIS)

1989-01-01

Further to the reecommendations for determining the surface contamination of the skin and estimating the radiation exposure of the skin after contamination (SAAS-Mitt--89-16), measures for skin decontamination are recommended. They are necessary if (1) after simple decontamination by means of water, soap and brush without damaging the skin the surface contamination limits are exceeded and the radiation exposure to be expected for the undamaged healthy skin is estimated as to high, and if (2) a wound is contaminated. To remove skin contaminations, in general universally applicable, non-aggressive decontamination means and methods are sufficient. In special cases, nuclide-specific decontamination is required taking into account the properties of the radioactive substance

Decontamination and decommissioning of 61 plutonium gloveboxes in D-Wing, Building 212 Argonne National Laboratory-East: Final project report

International Nuclear Information System (INIS)

Cheever, C.L.; Rose, R.W.

1996-09-01

Argonne National Laboratory-East (ANL-E) is a government-owned, contractor operated, multipurpose research facility located 25 miles southwest of downtown Chicago on 689 hectares (1,700 acres) in DuPage County, Illinois, as shown in Figure 1.1. Building 212 is located in the central area of ANL-E, as shown in Figure 1.2. The purpose of this project was to eliminate the risk of radioactive material release from the contaminated glovebox systems and to make the laboratories available for unrestricted use. The following work objectives were established: (1) Identify and remove radioactive materials for return to ANL-E Special Materials control. (2) Remove and package the radioactively contaminated materials and equipment from the gloveboxes. (3) Decontaminate the gloveboxes to nontransuranic (non-TRU) levels. (4) Size-reduce and package the gloveboxes and support systems. (5) Document and dispose of the radioactive and mixed waste. (6) Decontaminate, survey, and release the nine laboratories and corridor areas for unrestricted use

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)

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

International Nuclear Information System (INIS)

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

1990-01-01

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

Decontamination Data - Blister Agents

Data.gov (United States)

U.S. Environmental Protection Agency — Decontamination efficacy data for blister agents on various building materials using various decontamination solutions. This dataset is associated with the following...

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...

Decontamination of soils and materials containing medium-fired PuO{sub 2} using inhibited fluorides with polymer filtration technology

Energy Technology Data Exchange (ETDEWEB)

Temer, D.J.; Villarreal, R.; Smith, B.F. [Los Alamos National Lab., NM (United States)

1997-10-01

The decontamination of soils and/or materials from medium-fired plutonium oxide (PuO{sub 2}) with an effective and efficient decontamination agent that will not significantly dissolve the matrix requires a new and innovative technology. After testing several decontamination agents and solutions for dissolution of medium-fired PuO{sub 2}, the most successful decontamination solutions were fluoride compounds, which were effective in breaking the Pu-oxide bond but would not extensively dissolve soil constituents and other materials. The fluoride compounds, tetra fluoboric acid (HBF{sub 4}) and hydrofluorosilicic acid (H{sub 2}F{sub 6}Si), were effective in dissolving medium-fired PuO{sub 2}, and did not seem to have the potential to dissolve the matrix. In both compounds, the fluoride atom is attached to a boron or silicon atom that inhibits the reactivity of the fluoride towards other compounds or materials containing atoms less attracted to the fluoride atom in an acid solution. Because of this inhibition of the reactivity of the fluoride ion, these compounds are termed inhibited fluoride compounds or agents. Both inhibited fluorides studied effectively dissolved medium-fired PuO{sub 2} but exhibited a tendency to not attack stainless steel or soil. The basis for selecting inhibited fluorides was confirmed during leaching tests of medium-fired PuO{sub 2} spiked into soil taken from the Idaho National Engineering Laboratory (INEL). When dissolved in dilute HNO{sub 3}, HCl, or HBr, both inhibited fluoride compounds were effective at solubilizing the medium-fired PuO{sub 2} from spiked INEL soil.

Recovery of plutonium and americium from chloride salt wastes by solvent extraction

International Nuclear Information System (INIS)

Reichley-Yinger, L.; Vandegrift, G.F.

1987-01-01

Plutonium and americium can be recovered from aqueous waste solutions containing a mixture of HCl and chloride salt wastes by the coupling of two solvent extraction systems: tributyl phosphate (TBP) in tetrachloroethylene (TCE) and octyl(phenyl)-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO) in TCE. In the flowsheet developed, the salt wastes are dissolved in HCl, the Pu(III) is oxidized to the IV state with NaClO 2 and recovered in the TBP-TCE cycle, and the Am is then removed from the resultant raffinate by the CMPO-TCE cycle. The consequences of the feed solution composition and extraction behavior of these species on the process flowsheet design, the Pu-product purity, and the decontamination of the aqueous raffinate from transuranic elements are discussed. 16 refs., 6 figs

Strippable gel for decontamination of contaminated metallic surfaces

International Nuclear Information System (INIS)

Banerjee, D.; Sandhya, U.; Khot, S.A.; Srinivas, C.; Wattal, P.K.

2013-01-01

(II). Decontamination efficacy of the gel was confirmed by application on SS tray (42 x 81 cm) contaminated with 60 Co. The gel could be easily peeled off as a single sheet and average decontamination efficiency of more than 99% was achieved. The amount of spent gel generated from application on the SS tray is about 25 g and can be held within a palm as can be seen in the paper. (author)

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

Estimation of environmental transfer of plutonium and the dose to man

International Nuclear Information System (INIS)

1981-09-01

The need to examine the behaviour of individual radionuclides in the environment is stressed. Sometimes unique pathways of exposure exist and more specialized methods of dose estimation could be considered. The toxicity of the alpha emitting plutonium isotopes is of concern and their long half-lives lead to persistence in the environment and long-term potential for exposing man. Some formulas are therefore presented for making preliminary estimates of environmental transfer and dose for the radioisotopes of the element plutonium. Exposure of man to plutonium in the environment may occur by inhalation or ingestion - the inhalation and ingestion intake rates for which specific pathways have been considered are listed. The primary pathway to man is the inhalation intake; the most important ingestion intake is the consumption of plant foods due to the greater concentration achieved and the higher consumption rates of these foods. Also discussed is plutonium in the nuclear fuel cycle, the release of plutonium from current nuclear installations, the occurrence of plutonium from weapons fallout, airborne releases of plutonium (concentration in the air, deposition rate, resuspension, transfer to plants - foliar and root uptake - transfer to milk, etc.), liquid release (concentration in water, transfer to drinking water, to fish, to plants by irrigation, to milk, to meat). The importance of the release situation and local environment conditions including land and water utilization, population factors and habits for any further investigation is pointed out

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

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)

Development of new chemical and electrochemical decontamination methods for selected equipment of WWER-440 and WWER-1000 reactor primary circuit

International Nuclear Information System (INIS)

Solcanyi, M.; Majersky, D.

1998-01-01

Special devices for in-situ application of decontamination technologies assigned for Steam Generator, Pressurizer and Main Circulating Casing of WWER-1000 type were designed, manufactured and tested in real conditions of their use in above Primary Circuit components. New decontamination technologies like low-concentration process NP-NHN for the decontamination of the Steam Generator, combined chemico-mechanical treatment for the Pressurizer and semi-dry electrolysis for the Main Circulating Pump Casing were developed and approved for their safe plant application from point of view of decontamination efficiency, corrosion influence and processing of secondary wastes. Main technological parameters were defined to achieve high decontamination efficiency and corrosion-safe application of all decontamination technologies. (author)

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

Some remarks about decontamination

International Nuclear Information System (INIS)

Bertini, A.

1990-01-01

Decontamination in itself is not the elimination of a problem, but corresponds to move that problem from one place to another. It is beneficial only if the contamination is less of a nuisance when moved to the ''other place''. Therefore any prospective decontamination process is to be considered essentially in terms of cost-benefit, and in particular in terms of reducing the burden on the waste management systems. The paper is not intended to deal with and to review critically the technical aspects of the various decontamination processes which are currently available. Its aim is to call the attention of those who may be faced with the problem of large-scale decontamination, so that this operation is carried out after all practical aspects have been examined. (author)

Characterization of plutonium-bearing wastes by chemical analysis and analytical electron microscopy

International Nuclear Information System (INIS)

Behrens, R.G.; Buck, E.C.; Dietz, N.L.; Bates, J.K.; Van Deventer, E.; Chaiko, D.J.

1995-09-01

This report summarizes the results of characterization studies of plutonium-bearing wastes produced at the US Department of Energy weapons production facilities. Several different solid wastes were characterized, including incinerator ash and ash heels from Rocky Flats Plant and Los Alamos National Laboratory; sand, stag, and crucible waste from Hanford; and LECO crucibles from the Savannah River Site. These materials were characterized by chemical analysis and analytical electron microscopy. The results showed the presence of discrete PuO 2 PuO 2-x , and Pu 4 O 7 phases, of about 1μm or less in size, in all of the samples examined. In addition, a number of amorphous phases were present that contained plutonium. In all the ash and ash heel samples examined, plutonium phases were found that were completely surrounded by silicate matrices. Consequently, to achieve optimum plutonium recovery in any chemical extraction process, extraction would have to be coupled with ultrafine grinding to average particle sizes of less than 1 μm to liberate the plutonium from the surrounding inert matrix

Experimental evaluation of washing for treatment of combustible plutonium-contaminated materials

International Nuclear Information System (INIS)

Wilkins, J.D.; Wisbey, S.J.

1983-03-01

Laboratory scale experiments have been carried out in order to assess the potential of washing as a method for removing plutonium from contaminated combustible wastes. A wide range of aqueous (eg 1 M HNO 3 , 1 M NaOH) and organic (1,1,2-trichlorotrifluoroethane) reagents have been investigated. Both synthetically contaminated and real wastes have been investigated. The preferred wash reagent has been identified as 1 M sodium hydroxide solution; plutonium recoveries of ca.80 to 90% can be achieved. (author)

Decontamination in the Republic of Belarus

International Nuclear Information System (INIS)

Antsipov, G.V.; Matveenko, S.A.; Mirkhaidarov, A.Kh.

2002-01-01

To continue the decontamination work in the Republic of Belarus, which was carried out by the military troops, the state specialized enterprises were formed in Gomel and Mogilev in 1991. The organization and regulations were developed inside the country: instructions, rules, radiological and hygienic criteria and norms. The enterprises concentrated on decontamination of the most socially significant facilities: kindergartens, schools, medical institutions and industrial enterprises. During 9 years Gomel State Specialized Enterprise 'Polessje' decontaminated 130 kindergartens, schools and hospitals. The total decontaminated area was 450 000 m 2 . The ventilation systems and equipment at 27 industrial enterprises in Gomel were decontaminated. The practical decontamination methods for areas, buildings, roofs, industrial equipment, ventilation systems were developed and tested. The special rules for handling wastes contaminated with Cs were elaborated. The paper analyzes and sums up the acquired experience which is important for implementation of rehabilitation programs and improvement of decontamination methods. (author)

Chemistry research and development. Annual progress report, November 1, 1979-October 31, 1980

International Nuclear Information System (INIS)

Miner, F.J.

1981-01-01

Chemistry R and D is involved in a number of programs. These programs include process support to Rocky Flats production operations, development of pyrochemical processes for plutonium recovery and purification in addition to integration of these processes into production, actinide separation research, determination of thermodynamic properties of plutonium and plutonium compounds, preparation of special alloys for use in radiochemical tracer programs, development of processes for decontaminating plutonium and plutonium compounds, preparation of special alloys for use in radiochemical tracer programs, development of processes for decontaminating plutonium-contaminated soils, characterization of the surfaces of various metals, and investigating the mechanisms and kinetics of the plutonium-hydrogen-oxygen systems. Some specific highlights for the report period include the following: (1) as part of the ongoing soil decontamination program at Rocky Flats, a site survey was completed in which data on contaminated soils in the United States were assembled and a set of soil contamination criteria was proposed to govern the disposition of effluent soil fractions from a soil decontamination process; (2) a series of disks were prepared for a Radiochemical Diagnostic Tracer Program from plutonium-242 and from an alloy of cerium and americium-241; (3) a material balance around past and current americium recovery processes was completed; (4) the technical feasibility of the pyroredox process was established for purification of plutonium in a tilt-pour furnace; and (5) in the continuing investigation of the plutonium-hydrogen system, it was shown that the kinetics of the hydriding of plutonium in a powder form is proportional to the hydrogen pressure below a pressure of 1000 Pa and is independent of the hydrogen pressure above 1000 Pa

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.

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

Determination of overall decontamination factors for common impurity elements in PHWR spent fuel reprocessing

International Nuclear Information System (INIS)

Pant, D.K.; Bhalerao, B.A.; Gupta, K.K.; Kulkarni, P.G.; Gurba, P.B.; Janardan, P.; Changrani, R.D.; Dey, P.K.

2009-01-01

An attempt has been made to determine overall decontamination factors for elemental impurities normally encountered in the U 3 O 8 product obtained by reprocessing of PHWR spent fuel. The solution obtained by dissolution of spent fuel and corresponding U 3 O 8 product were analyzed for 24 elemental impurities by ICP-AES for this purpose. Decontamination factors achieved for major neutron poisons are in the range of 200-400. (author)

Ultratrace analysis of uranium and plutonium by mass spectrometry

International Nuclear Information System (INIS)

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

2002-01-01

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

Long lasting decontamination foam

Science.gov (United States)

Demmer, Ricky L.; Peterman, Dean R.; Tripp, Julia L.; Cooper, David C.; Wright, Karen E.

2010-12-07

Compositions and methods for decontaminating surfaces are disclosed. More specifically, compositions and methods for decontamination using a composition capable of generating a long lasting foam are disclosed. Compositions may include a surfactant and gelatin and have a pH of less than about 6. Such compositions may further include affinity-shifting chemicals. Methods may include decontaminating a contaminated surface with a composition or a foam that may include a surfactant and gelatin and have a pH of less than about 6.

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

Chemical Gel for Surface Decontamination

International Nuclear Information System (INIS)

Jung, Chong Hun; Moon, J. K.; Won, H. J.; Lee, K. W.; Kim, C. K.

2010-01-01

Many chemical decontamination processes operate by immersing components in aggressive chemical solutions. In these applications chemical decontamination technique produce large amounts of radioactive liquid waste. Therefore it is necessary to develop processes using chemical gels instead of chemical solutions, to avoid the well-known disadvantages of chemical decontamination techniques while retaining their high efficiency. Chemical gels decontamination process consists of applying the gel by spraying it onto the surface of large area components (floors, walls, etc) to be decontaminated. The gel adheres to any vertical or complex surface due to their thixotropic properties and operates by dissolving the radioactive deposit, along with a thin layer of the gel support, so that the radioactivity trapped at the surface can be removed. Important aspects of the gels are that small quantities can be used and they show thixitropic properties : liquid during spraying, and solid when stationary, allowing for strong adherence to surfaces. This work investigates the decontamination behaviors of organic-based chemical gel for SS 304 metallic surfaces contaminated with radioactive materials

Decontamination manual of RI handling laboratory

International Nuclear Information System (INIS)

Wadachi, Yoshiki

2004-01-01

Based on experiences in Japan Atomic Energy Research Institute (JAERI), the essential and practical knowledge of radioactive contamination and its decontamination, and the method and procedure of floor decontamination are described for researcher and managing person in charge of handling radioisotopes (RI) in RI handling laboratories. Essential knowledge concerns the uniqueness of solid surface contamination derived from RI half lives and quantities, surface contamination density limit, and mode/mechanism of contamination. The principle of decontamination is a single conduct with recognition of chemical form of the RI under use. As the practical knowledge, there are physical and chemical methods of solid surface decontamination. The latter involves use of inorganic acids, chelaters and surfactants. Removal and replacement of contaminated solid like floor material are often effective. Distribution mapping of surface contamination can be done by measuring the radioactivity in possibly contaminated areas, and is useful for planning of effective decontamination. Floor surface decontamination is for the partial and spread areas of the floor. It is essential to conduct the decontamination with reagent from the highly to less contaminated areas. Skin decontamination with either neutral detergent or titanium oxide is also described. (N.I.)

Chemical decontamination: an overview

International Nuclear Information System (INIS)

Shaw, R.A.; Wood, C.J.

1985-01-01

The source of radioactive contamination in various types of power reactors is discussed. The methods of chemical decontamination vary with the manner in which the radioactive contaminants are deposited on the surface. Two types of dilute decontamination systems are available. One system uses organic acids and chelating agents, which are mildly reducing in nature. In this process, the oxide contaminants are removed by simple acidic dissolution and reductive dissolution. The second type of decontamination process is based on low oxidation state metal ions, which are more strongly reducing and do not require a corrosion inhibitor. All processes commercially available for decontamination of power reactors are not detailed here, but a few key issues to be considered in the selection of a process are highlighted. 2 figures, 2 tables

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)

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)

Spectrochemical determination of tantalum in plutonium metal using direct current plasma emission spectrometry

International Nuclear Information System (INIS)

Fadeff, S.K.; Morris, W.F.

1983-01-01

Tantalum is determined by direct current plasma spectrometry after separation of plutonium from solution as PuF 3 . After centrifugation of the PuF 3 precipitate, a low level of plutonium remains in solution in sufficient quantity to cause spectral interferences. It is necessary to determine the plutonium by dc plasma spectrometry and apply a correction to determine low tantalum concentrations with good accuracy and precision. Tantalum can be determined down to 0.4 ppM in solution with a relative standard deviation of 10 percent. Better precision can be achieved at higher concentrations. The procedure is simple and convenient for glovebox work. 5 references, 1 figure, 1 table

Trace analysis of plutonium in environmental samples by resonance ionization mass spectroscopy (RIMS)

International Nuclear Information System (INIS)

Erdmann, N.; Herrmann, G.; Huber, G.; Koehler, S.; Kratz, J.V.; Mansel, A.; Nunnemann, M.; Passler, G.; Trautmann, N.; Waldek, A.

1997-01-01

Trace amounts of plutonium in the environment can be detected by resonance ionization mass spectroscopy (RIMS). An atomic beam of plutonium is produced after its chemical separation and deposition on a filament. The atoms are ionized by a three-step excitation using pulsed dye-lasers. The ions are mass-selectively detected in a time-of-flight (TOF) mass spectrometer. With this setup a detection limit of 1·10 6 atoms of plutonium has been achieved. Furthermore, the isotopic composition can be determined. Different samples, including soil from the Chernobyl area, IAEA-certified sediments from the Mururoa Atoll and urine, have been investigated. copyright 1997 American Institute of Physics

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

Microbiological decontamination of Spirulina Platensis and green coffee using accelerated electron beams

International Nuclear Information System (INIS)

Nemtanu, Monica R.; Brasoveanu, Mirela; Minea, R.; Mitru, Ecaterina; Grecu, Maria Nicoleta; Albulescu, Mihaela

2006-01-01

Biological raw materials can be contaminated with microorganisms and to make them suitable for commercialization, the quality relative to microbial content is necessary to be achieved. Irradiation is a decontamination method for numerous foodstuffs, being a feasible, very effective and environment friendly procedure. The aim of the paper is to evaluate the possibility to apply the electron beam treatment on Spirulina Platensis and green coffee for biological decontamination. The cyanobacterium Spirulina and green coffee have been irradiated with electron beams up to 40 kGy. To determine the microbial load, antioxidant activity, and rheological behaviour the techniques of electron paramagnetic resonance (EPR) and absorption spectroscopy have been applied. The results showed that accelerated electron beams could be efficient to decontaminate Spirulina as well as green coffee without significant changes in their properties. (authors)

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

Situations of decontamination promotion activities. Efforts by Tokyo Electric Power Company, Fukushima Revitalization Headquarters, Decontamination Promotion Office

International Nuclear Information System (INIS)

Takano, Takahiko; Ito, Kei; Takizawa, Koichi

2015-01-01

As for the decontamination of the soil contaminated with radioactive materials, decontamination is on the way in compliance with the 'Act on Special Measures Concerning the Handling of Environmental Pollution by Radioactive Materials by the NPS Accident Associated with the Tohoku District - Off the Pacific Ocean' (hereinafter, the Act on Special Measures). Tokyo Electric Power Company (TEPCO), as the party concerned to the accident, is cooperating with decontamination activities conducted by countries and municipalities under the Act on Special Measures. Total number of people cooperated by the Decontamination Promotion Office amounts to about 120,000 people. The cooperation to the decontamination by countries and municipalities covers the following fields: provision of knowledge of radiation, training of site management and supervisors, and proposal such as the decontamination method suitable for the site. As cooperation to various monitoring, there is a traveling monitoring that performs radiation measurement from the vehicles. As cooperation in the farming and industrial resumption toward the reconstruction, the group has implemented support for the distribution promotion of the holdup that was stuck in distribution due to contamination with radioactive substances. As decontamination related technology, the following are performed: (1) preparation of radiation understanding promotion tool, (2) development of precise individual dose measurement technology, and (3) development and utilization of decontamination effect analysis program. In the future, this group will perform the follow-up for decontamination, and measures toward the lifting of evacuation order. It will install the basis to perform various technical analyses on decontamination, and will further intensify technical cooperation. (A.O.)

Safeguardability of the vitrification option for disposal of plutonium

Energy Technology Data Exchange (ETDEWEB)

Pillay, K.K.S. [Los Alamos National Lab., NM (United States)

1996-05-01

Safeguardability of the vitrification option for plutonium disposition is rather complex and there is no experience base in either domestic or international safeguards for this approach. In the present treaty regime between the US and the states of the former Soviet Union, bilaterial verifications are considered more likely with potential for a third-party verification of safeguards. There are serious technological limitations to applying conventional bulk handling facility safeguards techniques to achieve independent verification of plutonium in borosilicate glass. If vitrification is the final disposition option chosen, maintaining continuity of knowledge of plutonium in glass matrices, especially those containing boron and those spike with high-level wastes or {sup 137}Cs, is beyond the capability of present-day safeguards technologies and nondestructive assay techniques. The alternative to quantitative measurement of fissile content is to maintain continuity of knowledge through a combination of containment and surveillance, which is not the international norm for bulk handling facilities.

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

Chemical decontamination process and device therefor

International Nuclear Information System (INIS)

Takahashi, Ryota; Sakai, Hitoshi

1998-01-01

The present invention provides a process and a device for chemical decontamination, which can suppress corrosion of low corrosion resistant materials, keep decontamination properties substantially as same as before and further, reduce the volume of secondary wastes. In a step of reductively melting oxide membranes on an objective material to be decontaminated, a mixture of oxalic acid and a salt thereof is used as a reducing agent, and the reductive melting is conducted while suppressing hydrogen ion concentration of an aqueous liquid system. In order to enhance the reducibility of the oxalic acid ions, it is desirable to add a cyclic hetero compound thereto. The device of the present invention comprises, a decontamination loop including a member to be decontaminated, a heater and a pH meter, a medical injection pump for injecting a reducing agent to the decontamination loop, a metal ion recovering loop including an ion exchange resin tower, a reducing agent decomposing loop including an electrolytic vessel and/or a UV ray irradiation cell, a circulation pump for circulating the decontamination liquid to each of the loops and a plurality of opening/closing valves for switching the loop in which the decontamination liquid is circulated. (T.M.)

An intercomparison experiment on isotope dilution thermal ionisation mass spectrometry using plutonium-239 spike for the determination of plutonium concentration in dissolver solution of irradiated fuel

International Nuclear Information System (INIS)

Aggarwal, S.K.; Shah, P.M.; Saxena, M.K.; Jain, H.C.; Gurba, P.B.; Babbar, R.K.; Udagatti, S.V.; Moorthy, A.D.; Singh, R.K.; Bajpai, D.D.

1996-01-01

Determination of plutonium concentration in the dissolver solution of irradiated fuel is one of the key measurements in the nuclear fuel cycle. This report presents the results of an intercomparison experiment performed between Fuel Chemistry Division (FCD) at BARC and PREFRE, Tarapur for determining plutonium concentration in dissolver solution of irradiated fuel using 239 Pu spike in isotope dilution thermal ionisation mass spectrometry (ID-TIMS). The 239 Pu spike method was previously established at FCD as viable alternative to the imported enriched 242 Pu or 244 Pu; the spike used internationally for plutonium concentration determination by IDMS in dissolver solution of irradiated fuel. Precision and accuracy achievable for determining plutonium concentration are compared under the laboratory and the plant conditions using 239 Pu spike in IDMS. For this purpose, two different dissolver solutions with 240 Pu/ 239 Pu atom ratios of about 0.3 and 0.07 corresponding, respectively, to high and low burn-up fuels, were used. The results of the intercomparison experiment demonstrate that there is no difference in the precision values obtained under the laboratory and the plant conditions; with mean precision values of better than 0.2%. Further, the plutonium concentration values determined by the two laboratories agreed within 0.3%. This exercise, therefore, demonstrates that ID-TIMS method using 239 Pu spike can be used for determining plutonium concentration in dissolver solution of irradiated fuel, under the plant conditions. 7 refs., 8 tabs

Low impact plutonium glovebox D ampersand D

International Nuclear Information System (INIS)

Rose, R.W.

1995-01-01

A dilemma often encountered in decontamination and decommissioning operations is the lack of choice as to the location where the work is to be performed. Facility siting, laboratory location, and adjacent support areas were often determined based on criteria, which while appropriate at the time, are not always the most conducive to a D ampersand D project. One must learn to adapt and cope with as found conditions. High priority research activities, which cannot be interrupted, may be occurring in adjacent non-radiological facilities in the immediate vicinity where highly contaminated materials must be handled in the course of a D ampersand D operation. The execution of a project within such an environment involves a high level of coordination, cooperation, professionalism and flexibility among the project, the work force and the surrounding occupants. Simply moving occupants from the potentially affected area is not always an option and much consideration must be given in the selection of the D ampersand D methodology to be employed and the processes to be implemented. Determining project boundaries and the ensuring that adjacent occupants are included in the planning/scheduling of specific operations which impact their work area are important in the development of the safety envelope. Such was the case in the recent D ampersand D of 61 gloveboxes contaminated with plutonium and other transuranic nuclides at the Argonne National Laboratory-East site. The gloveboxes, which were used in Department of Energy research and development program activities over the past 30 years, were decontaminated to below transuranic waste criteria, size reduced, packaged and removed from Building 212 by Argonne National Laboratory personnel in conjunction with Nuclear Fuel Services, Inc. with essentially no impact to adjacent occupants

The separation of silica nanoparticle by cetyltrimethylammonium bromide from decontamination foam waste

International Nuclear Information System (INIS)

Choi, Man Soo; Yoon, In Ho; Jung, Chong Hun; Moon, Jei Kwon; Choi, Wang Kyu

2016-01-01

Decontamination foam has been considered as a potential application for the cleaning of radioactive contaminant in the field of metallic walls, overhead surfaces, and complex components. Moreover, foam decontamination could generate the low secondary waste amount owing to its volume expansion. In order to increase the decontamination efficiency, it is essential to improve the foam stability with low amount of chemical decontamination agent. Yoon et al. reported that the silica nanoparticle containing surfactant increased the foam stability compared to only surfactant solution[3]. Nanoparticle has been used with surfactant, which they adsorb at fluid/fluid interface, to stabilize emulsions or bubbles in foams. Despite of improving foam stability, they still used the surfactant, silica nanoparticle (1 wt%), and viscosifier. In addition, it is difficult to separate silica nanoparticle from decontamination solution. Because nanoparticles differ from classical solid particles due to smaller particle size and their specific properties. Thus, the separation method for nanoparticle should be also developed with high recovery rates. The flocculation of silica nanoparticle added by CTAB could be quickly achieved for only 30 min. The particle size of SiO_2 was larger as CTAB amount increased, and SiO_2 contents in the top solution were decreased after centrifugation

The separation of silica nanoparticle by cetyltrimethylammonium bromide from decontamination foam waste

Energy Technology Data Exchange (ETDEWEB)

Choi, Man Soo; Yoon, In Ho; Jung, Chong Hun; Moon, Jei Kwon; Choi, Wang Kyu [KAERI, Daejeon (Korea, Republic of)

2016-05-15

Decontamination foam has been considered as a potential application for the cleaning of radioactive contaminant in the field of metallic walls, overhead surfaces, and complex components. Moreover, foam decontamination could generate the low secondary waste amount owing to its volume expansion. In order to increase the decontamination efficiency, it is essential to improve the foam stability with low amount of chemical decontamination agent. Yoon et al. reported that the silica nanoparticle containing surfactant increased the foam stability compared to only surfactant solution[3]. Nanoparticle has been used with surfactant, which they adsorb at fluid/fluid interface, to stabilize emulsions or bubbles in foams. Despite of improving foam stability, they still used the surfactant, silica nanoparticle (1 wt%), and viscosifier. In addition, it is difficult to separate silica nanoparticle from decontamination solution. Because nanoparticles differ from classical solid particles due to smaller particle size and their specific properties. Thus, the separation method for nanoparticle should be also developed with high recovery rates. The flocculation of silica nanoparticle added by CTAB could be quickly achieved for only 30 min. The particle size of SiO{sub 2} was larger as CTAB amount increased, and SiO{sub 2} contents in the top solution were decreased after centrifugation.

PWR decontamination feasibility study

Energy Technology Data Exchange (ETDEWEB)

Silliman, P.L.

1978-12-18

The decontamination work which has been accomplished is reviewed and it is concluded that it is worthwhile to investigate further four methods for decontamination for future demonstration. These are: dilute chemical; single stage strong chemical; redox processes; and redox/chemical in combination. Laboratory work is recommended to define the agents and processes for demonstration and to determine the effect of the solvents on PWR materials. The feasibility of Indian Point 1 for decontamination demonstrations is discussed, and it is shown that the system components of Indian Point 1 are well suited for use in demonstrations.

PWR decontamination feasibility study

International Nuclear Information System (INIS)

Silliman, P.L.

1978-01-01

The decontamination work which has been accomplished is reviewed and it is concluded that it is worthwhile to investigate further four methods for decontamination for future demonstration. These are: dilute chemical; single stage strong chemical; redox processes; and redox/chemical in combination. Laboratory work is recommended to define the agents and processes for demonstration and to determine the effect of the solvents on PWR materials. The feasibility of Indian Point 1 for decontamination demonstrations is discussed, and it is shown that the system components of Indian Point 1 are well suited for use in demonstrations

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

Dilute chemical decontamination program review

International Nuclear Information System (INIS)

Anstine, L.D.; Blomgren, J.C.; Pettit, P.J.

1980-01-01

The objective of the Dilute Chemical Decontamination Program is to develop and evaluate a process which utilizes reagents in dilute concentrations for the decontamination of BWR primary systems and for the maintenance of dose rates on the out-of-core surfaces at acceptable levels. A discussion is presented of the process concept, solvent development, advantages and disadvantages of reagent systems, and VNC loop tests. Based on the work completed to date it is concluded that (1) rapid decontamination of BWRs using dilute reagents is feasible; (2) reasonable reagent conditions for rapid chemical decontamination are: 0.01M oxalic acid + 0.005M citric acid, pH3.0, 90/degree/C, 0.5 to 1.0 ppm dissolved oxygen; (3) control of dissolved oxygen concentration is important, since high levels suppress the rate of decontamination and low levels allow precipitation of ferrous oxalate. 4 refs

HB-Line Plutonium Oxide Data Collection Strategy

Energy Technology Data Exchange (ETDEWEB)

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

2015-05-26

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

Study on LOMI decontamination technology

International Nuclear Information System (INIS)

Huang Fuduan; Yu Degui; Lu Jingju; Xie Yinyan

1993-10-01

The results of decontamination technique of Low-Oxidation-State Metal-Ion (LOMI) reagents developed from 1986 to 1991 in the laboratory are introduced. The experiments included preparation of LOMI reagents, de-filming efficiency, corrosion behavior of typical alloys, decontamination factors of reagents for contaminated materials and components have proved that the NP/LOMI decontamination method and treatment technique of waste water are feasible and have some advantages. The preparation of LOMI reagent with low concentration of formic acid by reduced pressure distilling technique and the utilization ratio of vanadium reached to 95% by second electrolysis are the main contributions of the study to the decontamination technique

Manual on decontamination of surfaces

International Nuclear Information System (INIS)

1979-01-01

The manual is intended for those who are responsible for the organization and implementation of decontamination programmes for facilities where radioactive materials are handled mainly on a laboratory scale. It contains information and guidelines on practical methods for decontaminating working spaces, equipment, laboratory benches and protective clothing. Useful information is also provided on the removal of loose skin contamination from personnel by mild, non-medical processes. Methods of removing skin contamination needing medical supervision, or of internal decontamination, which is entirely a medical process, are not covered in this manual. Large-scale decontamination of big nuclear facilities is also considered as outside its scope

Decontamination tests on cotton materials; Essais de decontamination sur tissus de coton

Energy Technology Data Exchange (ETDEWEB)

Cohen, P; Pelletier, C [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1958-07-01

It is shown that versene gives the best decontamination results on cotton materials soiled by a mixture of fission products. (author) [French] On a montre que le versene donne les meilleurs resultats de decontamination sur des tissus de coton souilles par un melange de produits de fission. (auteur)

Radioactivity decontamination of materials commonly used as surfaces in general-purpose radioisotope laboratories.

Science.gov (United States)

Leonardi, Natalia M; Tesán, Fiorella C; Zubillaga, Marcela B; Salgueiro, María J

2014-12-01

In accord with as-low-as-reasonably-achievable and good-manufacturing-practice concepts, the present study evaluated the efficiency of radioactivity decontamination of materials commonly used in laboratory surfaces and whether solvent spills on these materials affect the findings. Four materials were evaluated: stainless steel, a surface comprising one-third acrylic resin and two-thirds natural minerals, an epoxy cover, and vinyl-based multipurpose flooring. Radioactive material was eluted from a (99)Mo/(99m)Tc generator, and samples of the surfaces were control-contaminated with 37 MBq (100 μL) of this eluate. The same procedure was repeated with samples of surfaces previously treated with 4 solvents: methanol, methyl ethyl ketone, acetone, and ethanol. The wet radioactive contamination was allowed to dry and then was removed with cotton swabs soaked in soapy water. The effectiveness of decontamination was defined as the percentage of activity removed per cotton swab, and the efficacy of decontamination was defined as the total percentage of activity removed, which was obtained by summing the percentages of activity in all the swabs required to complete the decontamination. Decontamination using our protocol was most effective and most efficacious for stainless steel and multipurpose flooring. Moreover, treatment with common organic solvents seemed not to affect the decontamination of these surfaces. Decontamination of the other two materials was less efficient and was interfered with by the organic solvents; there was also great variability in the overall results obtained for these other two materials. In expanding our laboratory, it is possible for us to select those surface materials on which our decontamination protocol works best. © 2014 by the Society of Nuclear Medicine and Molecular Imaging, Inc.

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

Hot laboratory in Saclay. Equipment and radio-metallurgy technique of the hot lab in Saclay. Description of hot cell for handling of plutonium salts. Installation of an hot cell

International Nuclear Information System (INIS)

Bazire, R.; Blin, J.; Cherel, G.; Duvaux, Y.; Cherel, G.; Mustelier, J.P.; Bussy, P.; Gondal, G.; Bloch, J.; Faugeras, P.; Raggenbass, A.; Raggenbass, P.; Fufresne, J.

1959-01-01

Describes the conception and installation of the hot laboratory in Saclay (CEA, France). The construction ended in 1958. The main aim of this laboratory is to examine fuel rods of EL2 and EL3 as well as nuclear fuel studies. It is placed in between both reactors. In a first part, the functioning and specifications of the hot lab are given. The different hot cells are described with details of the ventilation and filtration system as well as the waste material and effluents disposal. The different safety measures are explained: description of the radiation protection, decontamination room and personnel monitoring. The remote handling equipment is composed of cutting and welding machine controlled with manipulators. Periscopes are used for sight control of the operation. In a second part, it describes the equipment of the hot lab. The unit for an accurate measurement of the density of irradiated uranium is equipped with an high precision balance and a thermostat. The equipment used for the working of irradiated uranium is described and the time length of each operation is given. There is also an installation for metallographic studies which is equipped with a manipulation bench for polishing and cleaning surfaces and a metallographic microscope. X-ray examination of uranium pellets will also be made and results will be compared with those of metallography. The last part describes the hot cells used for the manipulation of plutonium salts. The plutonium comes from the reprocessing plant and arrived as a nitric solution. Thus these cells are used to study the preparation of plutonium fluorides from nitric solution. The successive operations needed are explained: filtration, decontamination and extraction with TBP, purification on ion exchangers and finally formation of the plutonium fluorides. Particular attention has been given to the description of the specifications of the different gloveboxes and remote handling equipment used in the different reaction steps and

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

Melting metal waste for volume reduction and decontamination

International Nuclear Information System (INIS)

Copeland, G.L.; Heshmatpour, B.; Heestand, R.L.

1980-01-01

Melt-slagging was investigated as a technique for volume reduction and decontamination of radioactively contaminated scrap metals. Experiments were conducted using several metals and slags in which the partitioning of the contaminant U or Pu to the slag was measured. Concentrations of U or Pu in the metal product of about 1 ppM were achieved for many metals. A volume reduction of 30:1 was achieved for a typical batch of mixed metal scrap. Additionally, the production of granular products was demonstrated with metal shot and crushed slag

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)

Personnel decontamination and preventive skin care

International Nuclear Information System (INIS)

Henning, Klaus; Gojowczyk, Peter

2010-01-01

Skin contamination arises from contact with contaminated aqueous solutions and from transmission of radioactively contaminated dirt particles. As long as the surface of the skin is neither inflamed nor showing any lesions, normally only a limited part of the top layer (epidermis), i.e. the upper layers of the stratum corneum, is contaminated. The intact horny layer has a barrier function protecting against the penetration of chemicals and dirt particles. The horny layer can be damaged by water, solvents, alkaline substances, and acids. In general, it is safe to say that the horny layer acts as a natural barrier to the penetration of liquid and particulate impurities into lower layers of the skin. As long as the horny layer is intact and free from lesions, the risk of incorporation can be considered low. When decontaminating and cleansing the skin, also in daily skin cleansing, care must be taken to prevent the acid protective layer and the horny layer from being compromised. Daily cleansing and cleansing for decontamination must be carried out with a mild, weakly acidic detergent. In addition, prevention should be achieved daily by applying a non-greasy skin lotion to protect the skin. Following a systematic regular regimen in skin cleansing and preventive skin care as well as a specific approach in skin decontamination and cleansing will avoid damage to the skin and remove any contamination incurred. This approach comprises a three-pronged concept, namely skin protection, cleansing and care. (orig.)

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

Decontamination of floor surfaces

International Nuclear Information System (INIS)

Smirous, F.

1983-01-01

Requirements are presented put on the surfaces of floors of radiochemical workplaces. The mechanism is described of retaining the contaminant in the surface of the flooring, ways of reducing the hazards of floor surface contamination, decontamination techniques and used decontamination agents. (J.P.)

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.)

Reactive skin decontamination lotion (RSDL) for the decontamination of chemical warfare agent (CWA) dermal exposure.

Science.gov (United States)

Schwartz, M D; Hurst, C G; Kirk, M A; Reedy, S J D; Braue, E H

2012-08-01

Rapid decontamination of the skin is the single most important action to prevent dermal absorption of chemical contaminants in persons exposed to chemical warfare agents (CWA) and toxic industrial chemicals (TICs) as a result of accidental or intentional release. Chemicals on the skin may be removed by mechanical means through the use of dry sorbents or water. Recent interest in decontamination systems which both partition contaminants away from the skin and actively neutralize the chemical has led to the development of several reactive decontamination solutions. This article will review the recently FDA-approved Reactive Skin Decontamination Lotion (RSDL) and will summarize the toxicity and efficacy studies conducted to date. Evidence of RSDL's superior performance against vesicant and organophosphorus chemical warfare agents compared to water, bleach, and dry sorbents, suggests that RSDL may have a role in mass human exposure chemical decontamination in both the military and civilian arenas.

Decontamination measures for Fukushima prefecture. Fukushima prefecture measures for promoting decontamination

International Nuclear Information System (INIS)

Endo, Kouzou

2013-01-01

For Fukushima prefecture having suffered from significant damage associated with the Great East Japan Earthquake and the nuclear power plant accident, the decontamination work is the most urgent issue. The paper reports the present situation of the remediation acts of Fukushima Government done since the accident, particular emphasis on the removal of radioactive substances due to cesium 137 in the residential area. Government supports to promote the decontamination work and its operators, and encourages employers and employees in their efforts, to set up temporary storages of the produced radioactive wastes, to cultivate and improve technical supports for decontamination work and strengthen understanding and support of the local resident, thus providing the training course for the site supervisors, the person engaged in the work and management. (S. Ohno)

Summary of decontamination cover manufacturing experience

International Nuclear Information System (INIS)

Ulrich, G.B.; Berry, H.W.

1995-02-01

Decontamination cover forming cracks and vent cup assembly leaks through the decontamination covers were early manufacturing problems. The decontamination cover total manufacturing process yield was as low as 55%. Applicable tooling and procedures were examined. All manufacturing steps from foil fabrication to final assembly leak testing were considered as possible causes or contributing factors to these problems. The following principal changes were made to correct these problems: (1) the foil annealing temperature was reduced from 1375 degrees to 1250 degrees C, (2) the decontamination cover fabrication procedure (including visual inspection for surface imperfections and elimination of superfluous operations) was improved, (3) the postforming dye penetrant inspection procedure was revised for increased sensitivity, (4) a postforming (prewelding) 1250 degrees C/1 h vacuum stress-relief operation was added, (5) a poststress relief (prewelding) decontamination cover piece-part leak test was implemented, (6) the hold-down fixture used during the decontamination cover-to-cup weld was modified, and concomitantly, and (7) the foil fabrication process was changed from the extruding and rolling of 63-mm-diam vacuum arc-remelted ingots (extrusion process) to the rolling of 19-mm-square arc-melted drop castings (drop cast process). Since these changes were incorporated, the decontamination cover total manufacturing process yield has been 91 %. Most importantly, more than 99% of the decontamination covers welded onto vent cup assemblies were acceptable. The drastic yield improvement is attributed primarily to the change in the foil annealing temperature from 1375 degrees to 1250 degrees C and secondarily to the improvements in the decontamination cover fabrication procedure

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.

New measurements in plutonium L X ray emission spectrum using an electron probe micro-analyser

International Nuclear Information System (INIS)

Bobin, J.L.; Despres, J.

1966-01-01

Further studies by means of an electron-probe micro-analyser, allowed report CEA-R--1798 authors to set up a larger plutonium X ray spectrum table. Measurements of plutonium L II and L III levels excitation potentials have also been achieved. Some remarks about apparatus performance data (such as spectrograph sensibility, resolving power and accuracy) will be found in the appendix. (authors) [fr

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.

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)

Full system decontamination feasibility studies

International Nuclear Information System (INIS)

Denault, R.P.; LeSurf, J.E.; Walschot, F.W.

1988-01-01

Many chemical decontaminations have been performed on subsystems in light water reactors (BWRs and PWRs) but none on the full system (including the fuel) of large, (>500 MWe) investor owned reactors. Full system decontaminations on pressure-tubed reactors have been shown to facilitate maintenance, inspection, repair and replacement of reactor components. Further advantages are increased reactor availability and plant life extension. A conceptual study has been performed for EPRI (for PWRs) and Commonwealth Edison Co (for BWRs) into the applicability and cost benefit of full system decontaminations (FSD). The joint study showed that FSDs in both PWRs and BWRs, with or without the fuel included in the decontamination, are feasible and cost beneficial provided a large amount of work is to be done following the decontamination. The large amounts of radioactive waste generated can be managed using current technologies. Considerable improvements in waste handling, and consequent cost savings, can be obtained if new techniques which are now reaching commercial application are used. (author)

Fuel decontamination at Ringhals 1 with the new decontamination process IcedecTM

International Nuclear Information System (INIS)

Fredriksson, E.; Ivars, R.; Rosengren, A.; Granath, G.

2003-01-01

The new fuel decontamination technique ICEDEC TM , which has been developed by Westinghouse, is based on abrasion of fuel crud with ice particles. A mixture of ice and water is led continuously through the fuel assembly, which is placed in a specially designed fuel decontamination container connected to a closed loop recirculation system. The ice particles scrape off the loose crud from the fuel surfaces and a mixture of crud and water from the melted ice is then led to a filter unit were the crud is separated from the water. In this paper results of fuel decontamination tests of two-year-old and spent fuel assemblies during spring 2001 at Ringhals 1 are presented. The fuel crud was only released when ice particles passed through the fuel assembly and stopped within ten seconds after the feeding of ice particles had ceased. The activity release from the fuel could thus be performed in a controlled way making the process easy to manage and survey. Activity measurements confirmed that about 50% of the loose crud was removed from the fuel surfaces of the two-year-old assembly. Fuel inspection after the decontamination process showed no influence on the fuel integrity. Furthermore, no enhanced personnel radiation dose was involved with the fuel decontamination compared to normal fuel services. (authors)

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

International Nuclear Information System (INIS)

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

1990-12-01

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

Decontamination Technology Development for Nuclear Research Facilities

International Nuclear Information System (INIS)

Oh, Won Zin; Jung, Chong Hun; Choi, Wang Kyu; Won, Hui Jun; Kim, Gye Nam

2004-02-01

Technology development of surface decontamination in the uranium conversion facility before decommissioning, technology development of component decontamination in the uranium conversion facility after decommissioning, uranium sludge treatment technology development, radioactive waste soil decontamination technology development at the aim of the temporary storage soil of KAERI, Optimum fixation methodology derivation on the soil and uranium waste, and safety assessment methodology development of self disposal of the soil and uranium waste after decontamination have been performed in this study. The unique decontamination technology applicable to the component of the nuclear facility at room temperature was developed. Low concentration chemical decontamination technology which is very powerful so as to decrease the radioactivity of specimen surface under the self disposal level was developed. The component decontamination technology applicable to the nuclear facility after decommissioning by neutral salt electro-polishing was also developed. The volume of the sludge waste could be decreased over 80% by the sludge waste separation method by water. The electrosorption method on selective removal of U(VI) to 1 ppm of unrestricted release level using the uranium-containing lagoon sludge waste was tested and identified. Soil decontamination process and equipment which can reduce the soil volume over 90% were developed. A pilot size of soil decontamination equipment which will be used to development of real scale soil decontamination equipment was designed, fabricated and demonstrated. Optimized fixation methodology on soil and uranium sludge was derived from tests and evaluation of the results. Safety scenario and safety evaluation model were development on soil and uranium sludge aiming at self disposal after decontamination

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

The efficiency analysis methods of decontamination of Fukushima Prefecture territory (Japan

Directory of Open Access Journals (Sweden)

Dmitriy V. Aron

2017-01-01

per unit of prevented exposure dose for different emergency measures scenarios were estimated, including longterm and short-term evacuation and decontamination. The estimated values of the decontamination and the resettlement effectiveness were presented based on the comparison of the public costs and benefits.The author goes on argue that radiological effectiveness of the decontamination measures was very low. He noted that the measures were inconsistent with the principles of cost optimization in the world radiation protection standards. However, at the same time, the decontamination measures made it possible to prevent possible high costs to the government, and some positive social effects were finally achieved.

Hot laboratory in Saclay. Equipment and radio-metallurgy technique of the hot lab in Saclay. Description of hot cell for handling of plutonium salts. Installation of an hot cell; Laboratoire a tres haute activite de Saclay. Equipement et techniques radiometallurgiques du laboratoire a haute activite de Saclay. Description de cellules pour manipulation de sels de plutonium. Amenagement d'une cellule du laboratoire de haute activite

Energy Technology Data Exchange (ETDEWEB)

Bazire, R; Blin, J; Cherel, G; Duvaux, Y; Cherel, G; Mustelier, J P; Bussy, P; Gondal, G; Bloch, J; Faugeras, P; Raggenbass, A; Raggenbass, P; Fufresne, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1959-07-01

Describes the conception and installation of the hot laboratory in Saclay (CEA, France). The construction ended in 1958. The main aim of this laboratory is to examine fuel rods of EL2 and EL3 as well as nuclear fuel studies. It is placed in between both reactors. In a first part, the functioning and specifications of the hot lab are given. The different hot cells are described with details of the ventilation and filtration system as well as the waste material and effluents disposal. The different safety measures are explained: description of the radiation protection, decontamination room and personnel monitoring. The remote handling equipment is composed of cutting and welding machine controlled with manipulators. Periscopes are used for sight control of the operation. In a second part, it describes the equipment of the hot lab. The unit for an accurate measurement of the density of irradiated uranium is equipped with an high precision balance and a thermostat. The equipment used for the working of irradiated uranium is described and the time length of each operation is given. There is also an installation for metallographic studies which is equipped with a manipulation bench for polishing and cleaning surfaces and a metallographic microscope. X-ray examination of uranium pellets will also be made and results will be compared with those of metallography. The last part describes the hot cells used for the manipulation of plutonium salts. The plutonium comes from the reprocessing plant and arrived as a nitric solution. Thus these cells are used to study the preparation of plutonium fluorides from nitric solution. The successive operations needed are explained: filtration, decontamination and extraction with TBP, purification on ion exchangers and finally formation of the plutonium fluorides. Particular attention has been given to the description of the specifications of the different gloveboxes and remote handling equipment used in the different reaction steps and

Hot laboratory in Saclay. Equipment and radio-metallurgy technique of the hot lab in Saclay. Description of hot cell for handling of plutonium salts. Installation of an hot cell; Laboratoire a tres haute activite de Saclay. Equipement et techniques radiometallurgiques du laboratoire a haute activite de Saclay. Description de cellules pour manipulation de sels de plutonium. Amenagement d'une cellule du laboratoire de haute activite

Energy Technology Data Exchange (ETDEWEB)

Bazire, R.; Blin, J.; Cherel, G.; Duvaux, Y.; Cherel, G.; Mustelier, J.P.; Bussy, P.; Gondal, G.; Bloch, J.; Faugeras, P.; Raggenbass, A.; Raggenbass, P.; Fufresne, J. [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

1959-07-01

Describes the conception and installation of the hot laboratory in Saclay (CEA, France). The construction ended in 1958. The main aim of this laboratory is to examine fuel rods of EL2 and EL3 as well as nuclear fuel studies. It is placed in between both reactors. In a first part, the functioning and specifications of the hot lab are given. The different hot cells are described with details of the ventilation and filtration system as well as the waste material and effluents disposal. The different safety measures are explained: description of the radiation protection, decontamination room and personnel monitoring. The remote handling equipment is composed of cutting and welding machine controlled with manipulators. Periscopes are used for sight control of the operation. In a second part, it describes the equipment of the hot lab. The unit for an accurate measurement of the density of irradiated uranium is equipped with an high precision balance and a thermostat. The equipment used for the working of irradiated uranium is described and the time length of each operation is given. There is also an installation for metallographic studies which is equipped with a manipulation bench for polishing and cleaning surfaces and a metallographic microscope. X-ray examination of uranium pellets will also be made and results will be compared with those of metallography. The last part describes the hot cells used for the manipulation of plutonium salts. The plutonium comes from the reprocessing plant and arrived as a nitric solution. Thus these cells are used to study the preparation of plutonium fluorides from nitric solution. The successive operations needed are explained: filtration, decontamination and extraction with TBP, purification on ion exchangers and finally formation of the plutonium fluorides. Particular attention has been given to the description of the specifications of the different gloveboxes and remote handling equipment used in the different reaction steps and

Decontamination around the site of Chernobylsk; Decontamination autour du site de Tchernobyl

Energy Technology Data Exchange (ETDEWEB)

Manesse, D; Rzepka, J P; Maubert, H

1990-12-01

This report describes the decontamination of the site around the nuclear plant of Chernobylsk after the reactor accident of 1986. The work of decontamination in urban areas, buildings, fields and vegetation are detailed. The interventions to reduce the contamination of surface waters and to protect ground waters are also given. (N.C.).

Radiological analysis of plutonium glass batches with natural/enriched boron

International Nuclear Information System (INIS)

Rainisch, R.

2000-01-01

The disposition of surplus plutonium inventories by the US Department of Energy (DOE) includes the immobilization of certain plutonium materials in a borosilicate glass matrix, also referred to as vitrification. This paper addresses source terms of plutonium masses immobilized in a borosilicate glass matrix where the glass components include both natural boron and enriched boron. The calculated source terms pertain to neutron and gamma source strength (particles per second), and source spectrum changes. The calculated source terms corresponding to natural boron and enriched boron are compared to determine the benefits (decrease in radiation source terms) for to the use of enriched boron. The analysis of plutonium glass source terms shows that a large component of the neutron source terms is due to (a, n) reactions. The Americium-241 and plutonium present in the glass emit alpha particles (a). These alpha particles interact with low-Z nuclides like B-11, B-10, and O-17 in the glass to produce neutrons. The low-Z nuclides are referred to as target particles. The reference glass contains 9.4 wt percent B 2 O 3 . Boron-11 was found to strongly support the (a, n) reactions in the glass matrix. B-11 has a natural abundance of over 80 percent. The (a, n) reaction rates for B-10 are lower than for B-11 and the analysis shows that the plutonium glass neutron source terms can be reduced by artificially enriching natural boron with B-10. The natural abundance of B-10 is 19.9 percent. Boron enriched to 96-wt percent B-10 or above can be obtained commercially. Since lower source terms imply lower dose rates to radiation workers handling the plutonium glass materials, it is important to know the achievable decrease in source terms as a result of boron enrichment. Plutonium materials are normally handled in glove boxes with shielded glass windows and the work entails both extremity and whole-body exposures. Lowering the source terms of the plutonium batches will make the handling

Development of strippable gel for surface decontamination applications

International Nuclear Information System (INIS)

Banerjee, D.; Sandhya, U.; Khot, S.A.; Srinivas, C.

2015-07-01

Strippable gels are an attractive option for decontamination of surfaces particularly when materials are to be reused after decontamination. The process in general results in good decontamination performance with minimal secondary waste generation. This paper reports on development of strippable gel formulation using polyvinyl alcohol as the gel former. Peeling behavior of the gel film improved when glycerol was used as plasticizer. Incorporation of decontaminating agents is essential for the gel to be effective, so a number of decontaminating agents were screened based on their miscibility with the gel, smooth peeling, and good decontamination performance. Based on this study, a strippable gel, ‘INDIGEL’ was formulated as a potential candidate for surface decontamination applications. Extensive trials on evaluation of decontamination performance of Indigel were done on simulated surfaces like stainless steel tray, stainless steel fume hood, PVC floor, granite and ceramic table tops. Results show that Indigel is highly effective for decontamination of surfaces contaminated with all types of radionuclides. Simplicity of its use coupled with good decontamination ability will find application in nuclear and other chemical industries. (author)

Decontaminating method

International Nuclear Information System (INIS)

Furukawa, Toshiharu; Shibuya, Kiichiro.

1985-01-01

Purpose: To provide a method of eliminating radioactive contaminations capable of ease treatment for decontaminated liquid wastes and grinding materials. Method: Those organic grinding materials such as fine wall nuts shell pieces cause no secondary contaminations since they are softer as compared with inorganic grinding materials, less pulverizable upon collision against the surface to be treated, being capable of reusing and producing no fine scattering powder. In addition, they can be treated by burning. The organic grinding material and water are sprayed by a nozzle to the surface to be treated, and decontaminated liquid wastes are separated into solid components mainly composed of organic grinding materials and liquid components mainly composed of water by filtering. The thus separated solid components are recovered in a storage tank for reuse as the grinding material and, after repeating use, subjected to burning treatment. While on the other hand, water is recovered into a storage tank and, after repeating use, purified by passing through an ion exchange resin-packed column and decontaminated to discharge. (Horiuchi, T.)

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

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)