Plutonium and americium recovery from spent molten-salt-extraction salts with aluminum-magnesium alloys

International Nuclear Information System (INIS)

Cusick, M.J.; Sherwood, W.G.; Fitzpatrick, R.F.

1984-01-01

Development work was performed to determine the feasibility of removing plutonium and americium from spent molten-salt-extraction (MSE) salts using Al-Mg alloys. If the product buttons from this process are compatible with subsequent aqueous processing, the complex chloride-to-nitrate aqueous conversion step which is presently required for these salts may be eliminated. The optimum alloy composition used to treat spent 8 wt % MSE salts in the past yielded poor phase-disengagement characteristics when applied to 30 mol % salts. After a limited investigation of other alloy compositions in the Al-Mg-Pu-Am system, it was determined that the Al-Pu-Am system could yield a compatible alloy. In this system, experiments were performed to investigate the effects of plutonium loading in the alloy, excess magnesium, age of the spent salt on actinide recovery, phase disengagement, and button homogeneity. Experimental results indicate that 95 percent plutonium recoveries can be attained for fresh salts. Further development is required for backlog salts generated prior to 1981. A homogeneous product alloy, as required for aqueous processing, could not be produced

Addressing mixed waste in plutonium processing

International Nuclear Information System (INIS)

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

1991-01-01

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

Monitoring of wastes containing plutonium. Necessity and method

International Nuclear Information System (INIS)

Sousselier, Y.; Pottier, P.

1979-01-01

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

Plutonium waste incineration using pyrohydrolysis

International Nuclear Information System (INIS)

Meyer, M.L.

1991-01-01

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

Study of methods for removing strontium, plutonium, and ruthenium from Savannah River Plant waste supernate

International Nuclear Information System (INIS)

Wiley, J.R.

1976-06-01

As a part of long-term waste management studies at the Savannah River Laboratory, tests were made to study removal of strontium, plutonium, and ruthenium from simulated and actual waste supernates. Plutonium was sorbed by Duolite ARC-359 ion exchange resin, the same resin that is used to remove cesium from waste supernate. Strontium was removed from supernate by sorption on a chelating resin Chelex 100, or by precipitation as Sr 3 (PO 4 ) 2 . Activities of 137 Cs, 90 Sr, and 238-241 Pu remaining in processed waste supernate should be 1-10 nanocuries of each element per gram of salt. Of the methods that were tested, none was adequate for plant-scale removal of ruthenium

Applicability of molten salt oxidation to the destruction of actinide-contaminated wastes

International Nuclear Information System (INIS)

West, M.H.; Garcia, E.; Griego, W.J.; Court, D.B.; Rodriguez, L.

1992-01-01

A 1989 ban on incineration in the state of New Mexico caused cessation of actinide-contaminated cheesecloth, paper, and wood incineration within the Plutonium Facility (TA-55) at Los Alamos National Laboratory. Subsequently, plastic wipes were substituted for cheesecloth in the cleaning of glovebox interiors. However, waste minimization is not achieved by these measures since the wipes are discarded as Waste Isolation Pilot Plant certifiable wastes. After the ban was instituted, thermal decomposition of cheesecloth under argon at elevated temperature was examined and found satisfactory although scale of operation and speed were inferior to incineration. In 1991, the ban on incineration was lifted in New Mexico but Alamos has not chosen to pursue renewal of incineration at the Plutonium Facility. This paper reports that Los Alamos is looking from alternatives to incineration and thermal decomposition which are compatible with molten salt processing technology, historically a strength in actinide research at the Laboratory. Also, the technology must significantly reduce the volume of the waste upon treatment, i.e. waste minimization. Molten salt oxidation (MSO) has the promise of such a technology

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

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

International Nuclear Information System (INIS)

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

1987-02-01

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

Solubility and speciation of actinides in salt solutions and migration experiments of intermediate level waste in salt formations

International Nuclear Information System (INIS)

1986-01-01

A comprehensive study into the solubility of the actinides americium and plutonium in concentrated salt solutions, the release of radionuclides from various forms of conditioned ILW and the migration behaviour of these nuclides through geological material specific to the Gorleben site in Lower Saxony is described. A detailed investigation into the characterization of four highly concentrated salt solutions in terms of their pH, Eh, inorganic carbon contents and their densities is given and a series of experiments investigating the solubility of standard americium(III) and plutonium(IV) hydroxides in these solutions is described. Transuranic mobility studies for solutions derived from the standard hydroxides through salt and sand have shown the presence of at least two types of species present of widely differing mobility; one migrating with approximately the same velocity as the solvent front and the other strongly retarded. Actinide mobility data are presented and discussed for leachates derived from the simulated ILW in cement and data are also presented for the migration of the fission products in leachates derived from real waste solidified in cement and bitumen. Relatively high plutonium mobilities were observed in the case of the former and in the case of the real waste leachates, cesium was found to be the least retarded. The sorption of ruthenium was found to be largely associated with the insoluble residues of the natural rock salt rather than the halite itself. (orig./RB)

Study of the reaction of uranium and plutonium with bone char

International Nuclear Information System (INIS)

Silver, G.L.; Koenst, J.W.

1977-01-01

A study of the reaction of plutonium with a commercial bone char indicates that this bone char has a high capacity for removing plutonium from aqueous wastes. The adsorption of plutonium by bone char is pH dependent, and for plutonium(IV) polymer appears to be maximized near pH 7.3 for plutonium concentrations typical of some waste streams. Adsorption is affected by dissolved salts, especially calcium and phosphate salts. Freundlich isotherms representing the adsorption of uranium and plutonium have been prepared. The low potential imposed upon aqueous solutions by commercial bone char is adequate for reduction of hexavalent plutonium to a lower plutonium oxidation state

Waste salt recovery, recycle, and destruction

International Nuclear Information System (INIS)

Hickman, R.G.

1992-12-01

Starting in 1943 and continuing into the 1970s, radioactive wastes resulting from plutonium processing at Hanford were stored underground in 149 single shell tanks. Of these tanks, 66 are known or believedto be leaking, and over a period are believed to have leaked about 750,000 gal into the surrounding soil. The bulk of the aqueous solution has been removed and transferred to double shell tanks, none of which are leaking. The waste consists of 37 million gallons of salt cake and sludge. Most of the salt cake is sodium nitrate and other sodium salts. A substantial fraction of the sludge is sodium nitrate. Small amounts of the radionuclides are present in the sludge as oxides or hydroxides. In addition, some of the tanks contain organic compounds and ferrocyanide complexes, many of which have undergone radiolytic induced chemical changes during the years of storage. As part of the Hanford site remediation effort, the tank wastes must be removed, treated, and the residuals must be immobilized and disposed of in an environmentally acceptable manner. Removal methods of the waste from the tanks fall generally into three approaches: dry removal, slurry removal, and solution removed. The latter two methods are likely to result in some additional leakage to the surrounding soil, but that may be acceptable if the tank can be emptied and remediated before the leaked material permeates deeply into the soil. This effort includes three parts: salt splitting, acid separation, and destruction, with initial emphasis on salt splitting

Applications of molten salts in plutonium processing

International Nuclear Information System (INIS)

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

1987-01-01

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

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

Chemical Disposition of Plutonium in Hanford Site Tank Wastes

Energy Technology Data Exchange (ETDEWEB)

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

2015-05-07

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

Glovebox design requirements for molten salt oxidation processing of transuranic waste

International Nuclear Information System (INIS)

Ramsey, K.B.; Acosta, S.V.; Wernly, K.D.

1998-01-01

This paper presents an overview of potential technologies for stabilization of 238 Pu-contaminated combustible waste. Molten salt oxidation (MSO) provides a method for removing greater than 99.999% of the organic matrix from combustible waste. Implementation of MSO processing at the Los Alamos National Laboratory (LANL) Plutonium Facility will eliminate the combustible matrix from 238 Pu-contaminated waste and consequently reduce the cost of TRU waste disposal operations at LANL. The glovebox design requirements for unit operations including size reduction and MSO processing will be presented

Application of molten salt oxidation for the minimization and recovery of plutonium-238 contaminated wastes

International Nuclear Information System (INIS)

Wishau, R.

1998-05-01

Molten salt oxidation (MSO) is proposed as a 238 Pu waste treatment technology that should be developed for volume reduction and recovery of 238 Pu and as an alternative to the transport and permanent disposal of 238 Pu waste to the WIPP repository. In MSO technology, molten sodium carbonate salt at 800--900 C in a reaction vessel acts as a reaction media for wastes. The waste material is destroyed when injected into the molten salt, creating harmless carbon dioxide and steam and a small amount of ash in the spent salt. The spent salt can be treated using aqueous separation methods to reuse the salt and to recover 99.9% of the precious 238 Pu that was in the waste. Tests of MSO technology have shown that the volume of combustible TRU waste can be reduced by a factor of at least twenty. Using this factor the present inventory of 574 TRU drums of 238 Pu contaminated wastes is reduced to 30 drums. Further 238 Pu waste costs of $22 million are avoided from not having to repackage 312 of the 574 drums to a drum total of more than 4,600 drums. MSO combined with aqueous processing of salts will recover approximately 1.7 kilograms of precious 238 Pu valued at 4 million dollars (at $2,500/gram). Thus, installation and use of MSO technology at LANL will result in significant cost savings compared to present plans to transport and dispose 238 Pu TRU waste to the WIPP site. Using a total net present value cost for the MSO project as $4.09 million over a five-year lifetime, the project can pay for itself after either recovery of 1.6 kg of Pu or through volume reduction of 818 drums or a combination of the two. These savings show a positive return on investment

Glovebox design requirements for molten salt oxidation processing of transuranic waste

Energy Technology Data Exchange (ETDEWEB)

Ramsey, K.B.; Acosta, S.V. [Los Alamos National Lab., NM (United States); Wernly, K.D. [Molten Salt Oxidation Corp., Bensalem, PA (United States)

1998-12-31

This paper presents an overview of potential technologies for stabilization of {sup 238}Pu-contaminated combustible waste. Molten salt oxidation (MSO) provides a method for removing greater than 99.999% of the organic matrix from combustible waste. Implementation of MSO processing at the Los Alamos National Laboratory (LANL) Plutonium Facility will eliminate the combustible matrix from {sup 238}Pu-contaminated waste and consequently reduce the cost of TRU waste disposal operations at LANL. The glovebox design requirements for unit operations including size reduction and MSO processing will be presented.

Electrochemical studies on plutonium in molten salts

International Nuclear Information System (INIS)

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

2007-01-01

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

Elaboration and characterisation of plutonium waste reference materials

International Nuclear Information System (INIS)

Perolat, J.P.

1990-01-01

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

Application of molten salt oxidation for the minimization and recovery of plutonium-238 contaminated wastes

Energy Technology Data Exchange (ETDEWEB)

Wishau, R.

1998-05-01

Molten salt oxidation (MSO) is proposed as a {sup 238}Pu waste treatment technology that should be developed for volume reduction and recovery of {sup 238}Pu and as an alternative to the transport and permanent disposal of {sup 238}Pu waste to the WIPP repository. In MSO technology, molten sodium carbonate salt at 800--900 C in a reaction vessel acts as a reaction media for wastes. The waste material is destroyed when injected into the molten salt, creating harmless carbon dioxide and steam and a small amount of ash in the spent salt. The spent salt can be treated using aqueous separation methods to reuse the salt and to recover 99.9% of the precious {sup 238}Pu that was in the waste. Tests of MSO technology have shown that the volume of combustible TRU waste can be reduced by a factor of at least twenty. Using this factor the present inventory of 574 TRU drums of {sup 238}Pu contaminated wastes is reduced to 30 drums. Further {sup 238}Pu waste costs of $22 million are avoided from not having to repackage 312 of the 574 drums to a drum total of more than 4,600 drums. MSO combined with aqueous processing of salts will recover approximately 1.7 kilograms of precious {sup 238}Pu valued at 4 million dollars (at $2,500/gram). Thus, installation and use of MSO technology at LANL will result in significant cost savings compared to present plans to transport and dispose {sup 238}Pu TRU waste to the WIPP site. Using a total net present value cost for the MSO project as $4.09 million over a five-year lifetime, the project can pay for itself after either recovery of 1.6 kg of Pu or through volume reduction of 818 drums or a combination of the two. These savings show a positive return on investment.

Acid-digestion treatment of plutonium-containing waste

International Nuclear Information System (INIS)

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

1981-01-01

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

Preparation of plutonium waste forms with ICPP calcined high-level waste

Energy Technology Data Exchange (ETDEWEB)

Staples, B.A.; Knecht, D.A. [Lockheed Idaho Technologies Co., Idaho Falls, ID (United States); O`Holleran, T.P. [Argonne National Lab.-West, Idaho Falls, ID (United States)] [and others

1997-05-01

Glass and glass-ceramic forms developed for the immobilization of calcined high-level wastes generated by Idaho Chemical Processing Plant (ICPP) fuel reprocessing activities have been investigated for ability to immobilize plutonium and to simultaneously incorporate calcined waste as an anti-proliferation barrier. Within the forms investigated, crystallization of host phases result in an increased loading of plutonium as well as its incorporation into potentially more durable phases than the glass. The host phases were initially formed and characterized with cerium (Ce{sup +4}) as a surrogate for plutonium (Pu{sup +4}) and samarium as a neutron absorber for criticality control. Verification of the surrogate testing results were then performed replacing cerium with plutonium. All testing was performed with surrogate calcined high-level waste. The results of these tests indicated that a potentially useful host phase, based on zirconia, can be formed either by devitrification or solid state reaction in the glass studied. This phase incorporates plutonium as well as samarium and the calcined waste becomes part of the matrix. Its ease of formation makes it potentially useful in excess plutonium dispositioning. Other durable host phases for plutonium and samarium, including zirconolite and zircon have been formed from zirconia or alumina calcine through cold press-sintering techniques and hot isostatic pressing. Host phase formation experiments conducted through vitrification or by cold press-sintering techniques are described and the results discussed. Recommendations are given for future work that extends the results of this study.

Preparation of plutonium waste forms with ICPP calcined high-level waste

International Nuclear Information System (INIS)

Staples, B.A.; Knecht, D.A.; O'Holleran, T.P.

1997-05-01

Glass and glass-ceramic forms developed for the immobilization of calcined high-level wastes generated by Idaho Chemical Processing Plant (ICPP) fuel reprocessing activities have been investigated for ability to immobilize plutonium and to simultaneously incorporate calcined waste as an anti-proliferation barrier. Within the forms investigated, crystallization of host phases result in an increased loading of plutonium as well as its incorporation into potentially more durable phases than the glass. The host phases were initially formed and characterized with cerium (Ce +4 ) as a surrogate for plutonium (Pu +4 ) and samarium as a neutron absorber for criticality control. Verification of the surrogate testing results were then performed replacing cerium with plutonium. All testing was performed with surrogate calcined high-level waste. The results of these tests indicated that a potentially useful host phase, based on zirconia, can be formed either by devitrification or solid state reaction in the glass studied. This phase incorporates plutonium as well as samarium and the calcined waste becomes part of the matrix. Its ease of formation makes it potentially useful in excess plutonium dispositioning. Other durable host phases for plutonium and samarium, including zirconolite and zircon have been formed from zirconia or alumina calcine through cold press-sintering techniques and hot isostatic pressing. Host phase formation experiments conducted through vitrification or by cold press-sintering techniques are described and the results discussed. Recommendations are given for future work that extends the results of this study

Reclamation of plutonium from pyrochemical processing residues

International Nuclear Information System (INIS)

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

1987-04-01

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

Wastes from plutonium conversion and scrap recovery operations

Energy Technology Data Exchange (ETDEWEB)

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

1988-03-01

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

Wastes from plutonium conversion and scrap recovery operations

International Nuclear Information System (INIS)

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

1988-03-01

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

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

International Nuclear Information System (INIS)

Bouzigues, H.; Reneaud, J.M.

1963-01-01

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

Preparation of fused chloride salts for use in pyrochemical plutonium recovery operations at Los Alamos

Energy Technology Data Exchange (ETDEWEB)

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

1986-07-01

The Plutonium Metal Technology Group at Los Alamos routinely uses pyrochemical processes to produce and purify plutonium from impure sources. The basic processes (metal production, metal purification, and residue treatment) involve controlling oxidation and reduction reactions between plutonium and its compounds in molten salts. Current production methods are described, as well as traditional approaches and recent developments in the preparation of solvent salts for electrorefining, molten salt extraction, lean metal (pyroredox) purification, and direct oxide reduction.

Preparation of fused chloride salts for use in pyrochemical plutonium recovery operations at Los Alamos

International Nuclear Information System (INIS)

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

1986-07-01

The Plutonium Metal Technology Group at Los Alamos routinely uses pyrochemical processes to produce and purify plutonium from impure sources. The basic processes (metal production, metal purification, and residue treatment) involve controlling oxidation and reduction reactions between plutonium and its compounds in molten salts. Current production methods are described, as well as traditional approaches and recent developments in the preparation of solvent salts for electrorefining, molten salt extraction, lean metal (pyroredox) purification, and direct oxide reduction

Deep geologic disposal of mixed waste in bedded salt: The Waste Isolation Pilot Plant

International Nuclear Information System (INIS)

Rempe, N.T.

1993-01-01

Mixed waste (i.e., waste that contains both chemically hazardous and radioactive components) poses a moral, political, and technical challenge to present and future generations. But an international consensus is emerging that harmful byproducts and residues can be permanently isolated from the biosphere in a safe and environmentally responsible manner by deep geologic disposal. To investigate and demonstrate such disposal for transuranic mixed waste, derived from defense-related activities, the US Department of Energy has prepared the Waste Isolation Pilot Plant (WIPP) near Carlsbad, New Mexico. This research and development facility was excavated approximately at the center of a 600 m thick sequence of salt (halite) beds, 655 m below the surface. Proof of the long-term tectonic and hydrological stability of the region is supplied by the fact that these salt beds have remained essentially undisturbed since they were deposited during the Late Permian age, approximately 225 million years ago. Plutonium-239, the main radioactive component of transuranic mixed waste, has a half-life of 24,500 years. Even ten half-lives of this isotope - amounting to about a quarter million years, the time during which its activity will decline to background level represent only 0.11 percent of the history of the repository medium. Therefore, deep geologic disposal of transuranic mixed waste in Permian bedded salt appears eminently feasible

Measurement of plutonium and americium in molten salt residues

International Nuclear Information System (INIS)

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

1979-01-01

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

Preventing pollution from plutonium processing

International Nuclear Information System (INIS)

Pillay, K.K.S.

1993-01-01

The plutonium processing facility at Los Alamos has adopted the strategic goal of becoming a facility that processes plutonium in a way that produces only environmentally benign waste streams. Pollution prevention through source reduction and environmentally sound recycling are being pursued. General approaches to waste reductions are administrative controls, modification of process technologies, and additional waste polishing. Recycling of waste materials, such as spent acids and salts, are technical possibilities and are being pursued to accomplish additional waste reduction. Liquid waste stream polishing to remove final traces of plutonium and hazardous chemical constituents is accomplished through (a) process modifications, (b) use of alternative chemicals and sorbents for residue removal, (c) acid recycling, and (d) judicious use of a variety of waste polishing technologies. Technologies that show promise in waste minimization and pollution prevention are identified. Working toward this goal of pollution prevention is a worthwhile endeavor, not only for Los Alamos, but for the Nuclear Complex of the future

Preventing pollution from plutonium processing

International Nuclear Information System (INIS)

Pillay, K.K.S.

1995-01-01

The plutonium processing facility at Los Alamos has adopted the strategic goal of becoming a facility that processes plutonium in a way that produces only environmentally benign waste streams. Pollution prevention through source reduction and environmentally sound recycling are being pursued. General approaches to waste reductions are administrative controls, modification of process technologies, and additional waste polishing. Recycling of waste materials, such as spent acids and salts, are technical possibilities and are being pursued to accomplish additional waste reduction. Liquid waste stream polishing to remove final traces of plutonium and hazardous chemical constituents is accomplished through process modifications, use of alternative chemicals and sorbents for residue removal, acid recycling, and judicious use of a variety of waste polishing technologies. Technologies that show promise in waste minimization and pollution prevention are identified. Working toward this goal of pollution prevention is a worthwhile endeavor , not only for Los Alamos, but for the Nuclear Complex of the future. (author) 12 refs.; 2 figs

Waste minimization at a plutonium processing facility

International Nuclear Information System (INIS)

Pillay, K.K.S.

1995-01-01

As part of Los Alamos National Laboratory's (LANL) mission to reduce the nuclear danger throughout the world, the plutonium processing facility at LANL maintains expertise and skills in nuclear weapons technologies as well as leadership in all peaceful applications of plutonium technologies, including fuel fabrication for terrestrial and space reactors and heat sources and thermoelectric generators for space missions. Another near-term challenge resulted from two safety assessments performed by the Defense Nuclear Facilities Safety Board and the U.S. Department of Energy during the past two years. These assessments have necessitated the processing and stabilization of plutonium contained in tons of residues so that they can be stored safely for an indefinite period. This report describes waste streams and approaches to waste reduction of plutonium management

Direct reduction of plutonium from dicesium hexachloroplutonate

International Nuclear Information System (INIS)

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

1991-01-01

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

Determination of plutonium 241 in solutions of nuclear wastes

International Nuclear Information System (INIS)

Raymond, A.; Bilcot, J.B.; Poletiko, C.

1990-09-01

Determination of plutonium 241 in nuclear wastes is important because of long period and high energy of some daughter products. In this report are presented two quantitative analysis methods using both scintillation techniques: A complete method, in any case, by selective extraction of plutonium on an anionic resin allowing simultaneous determination of Pu 241 and the sum of other plutonium isotopes; a simplified method when alpha activity is higher than beta/gamma activity by liquid extraction with TTA. These methods are applied for analysis of 4 waste types: cement encapsulated wastes, bitumen encapsulated wastes, incineration ashes, leaching of encapsulated incineration ashes. In these 4 examples, Pu 241 activity is equal or higher than the sum of alpha plutonium isotope activity. Separation efficiency, measured from Pu 239 or with Pu 236 as tracer, is between 90 and 99% [fr

Molten salt combustion of radioactive wastes

International Nuclear Information System (INIS)

Grantham, L.F.; McKenzie, D.E.; Richards, W.L.; Oldenkamp, R.D.

1976-01-01

The Atomics International Molten Salt Combustion Process reduces the weight and volume of combustible β-γ contaminated transuranic waste by utilizing air in a molten salt medium to combust organic materials, to trap particulates, and to react chemically with any acidic gases produced during combustion. Typically, incomplete combustion products such as hydrocarbons and carbon monoxide are below detection limits (i.e., 3 ) is directly related to the sodium chloride vapor pressure of the melt; >80% of the particulate is sodium chloride. Essentially all metal oxides (combustion ash) are retained in the melt, e.g., >99.9% of the plutonium, >99.6% of the europium, and >99.9% of the ruthenium are retained in the melt. Both bench-scale radioactive and pilot scale (50 kg/hr) nonradioactive combustion tests have been completed with essentially the same results. Design of three combustors for industrial applications are underway

Supplemental technical information in support of Y/OWI/TM--44. Volume 17. Drawings for repository preconceptual design studies: BPNL waste forms in salt

International Nuclear Information System (INIS)

1978-04-01

Volume 17 contains drawings of a preconceptual design for a nuclear waste storage facility in salt. Three full cycles are considered: full recycle, throwaway cycle, and uranium recycle with plutonium in high-level waste

Los Alamos Plutonium Facility newly generated TRU waste certification

International Nuclear Information System (INIS)

Gruetzmacher, K.; Montoya, A.; Sinkule, B.; Maez, M.

1997-01-01

This paper presents an overview of the activities being planned and implemented to certify newly generated contact handled transuranic (TRU) waste produced by Los Alamos National Laboratory's (LANL's) Plutonium Facility. Certifying waste at the point of generation is the most important cost and labor saving step in the WIPP certification process. The pedigree of a waste item is best known by the originator of the waste and frees a site from expensive characterization activities such as those associated with legacy waste. Through a cooperative agreement with LANLs Waste Management Facility and under the umbrella of LANLs WIPP-related certification and quality assurance documents, the Plutonium Facility will be certifying its own newly generated waste. Some of the challenges faced by the Plutonium Facility in preparing to certify TRU waste include the modification and addition of procedures to meet WIPP requirements, standardizing packaging for TRU waste, collecting processing documentation from operations which produce TRU waste, and developing ways to modify waste streams which are not certifiable in their present form

Estimates of relative areas for the disposal in bedded salt of LWR wastes from alternative fuel cycles

International Nuclear Information System (INIS)

Lincoln, R.C.; Larson, D.W.; Sisson, C.E.

1978-01-01

The relative mine-level areas (land use requirements) which would be required for the disposal of light-water reactor (LWR) radioactive wastes in a hypothetical bedded-salt formation have been estimated. Five waste types from alternative fuel cycles have been considered. The relative thermal response of each of five different site conditions to each waste type has been determined. The fuel cycles considered are the once-through (no recycle), the uranium-only recycle, and the uranium and plutonium recycle. The waste types which were considered include (1) unreprocessed spent reactor fuel, (2) solidified waste derived from reprocessing uranium oxide fuel, (3) plutonium recovered from reprocessing spent reactor fuel and doped with 1.5% of the accompanying waste from reprocessing uranium oxide fuel, (4) waste derived from reprocessing mixed uranium/plutonium oxide fuel in the third recycle, and (5) unreprocessed spent fuel after three recycles of mixed uranium/plutonium oxide fuels. The relative waste-disposal areas were determined from a calculated value of maximum thermal energy (MTE) content of the geologic formations. Results are presented for each geologic site condition in terms of area ratios. Disposal area requirements for each waste type are expressed as ratios relative to the smallest area requirement (for waste type No. 2 above). For the reference geologic site condition, the estimated mine-level disposal area ratios are 4.9 for waste type No. 1, 4.3 for No. 3, 2.6 for No. 4, and 11 for No. 5

Technical support for GEIS: radioactive waste isolation in geologic formations. Volume 16. Repository preconceptual design studies: BPNL waste forms in salt

International Nuclear Information System (INIS)

1978-04-01

This volume, Volume 16, ''Repository Preconceptual Design Studies: BPNL Waste Forms in Salt,'' is one of a 23 volume series, ''Technical Support for GEIS: Radioactive Waste Isolation in Geologic Formations,'' Y/OWI/TM-36, which supplements the ''Contribution to Draft Generic Environmental Impact Statement on Commercial Waste Management: Radioactive Waste Isolation in Geologic Formations,'' Y/OWI/TM-44. The series provide a more complete technical basis for the preconceptual designs, resource requirements, and environmental source terms associated with isolating commercial LWR wastes in underground repositories in salt, granite, shale and basalt. Wastes are considered from three fuel cycles: uranium and plutonium recycling, no recycling of spent fuel and uranium-only recycling. This document describes a preconceptual design for a nuclear waste storage facility in salt. The waste forms assumed to arrive at the repository were supplied by Battelle Pacific Northwest Laboratories (BPNL). The facility design consists of several chambers excavated deep within a geologic formation together with access shafts and supportive surface structures. The facility design provides for: receiving and unloading waste containers; lowering them down shafts to the mine level; transporting them to the proper storage area and emplacing them in mined storage rooms. Drawings of the facility design are contained in TM-36/17, ''Drawings for Repository Preconceptual Design Studies: BPNL Waste Forms in Salt.''

Plutonium-238 alpha-decay damage study of the ceramic waste form

International Nuclear Information System (INIS)

Frank, S. M.; Barber, T. L.; Cummings, D.G.; DiSanto, T.; Esh, D.W.; Giglio, J. J.; Goff, K. M.; Johnson, S.G.; Kennedy, J.R.; Jue, J-F; Noy, M.; O'Holleran, T.P.; Sinkler, W.

2006-01-01

An accelerated alpha-decay damage study of a glass-bonded sodalite ceramic waste form has recently been completed. The purpose of this study was to investigate the physical and chemical durability of the waste form after significant exposure to alpha decay. This accelerated alpha-decay study was performed by doping the ceramic waste form with 238 Pu which has a much greater specific activity than 239 Pu that is normally present in the waste form. The alpha-decay dose at the end of the four year study was approximately 1 x 10 18 alpha-decays/gram of material. An equivalent time period for a similar dose of 239 Pu would require approximately 1100 years. After four years of exposure to 238 Pu alpha decay, the investigation observed little change to the physical or chemical durability of the ceramic waste form (CWF). Specifically, the 238 Pu-loaded CWF maintained it's physical integrity, namely that the density remained constant and no cracking or phase de-bonding was observed. The materials chemical durability and phase stability also did not change significantly over the duration of the study. The only significant measured change was an increase of the unit-cell lattice parameters of the plutonium oxide and sodalite phases of the material and an increase in the release of salt components and plutonium of the waste form during leaching tests, but, as mentioned, these did not lead to any overall loss of waste form durability. The principal findings from this study are: (1) 238 Pu-loaded CWF is similar in microstructure and phase composition to referenced waste form. (2) Pu was observed primarily as oxide comprised of aggregates of nano crystals with aggregates ranging in size from submicron to twenty microns in diameter. (3) Pu phases were primarily found in the intergranular glassy regions. (4) PuO phase shows expected unit cell volume expansion due to alpha decay damage of approximately 0.7%, and the sodalite phase unit cell volume has expanded slightly by 0.3% again

Los Alamos Plutonium Facility Waste Management System

International Nuclear Information System (INIS)

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

1997-01-01

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

Using Aspen simulation package to determine solubility of mixed salts in TRU waste evaporator bottoms

Energy Technology Data Exchange (ETDEWEB)

Hatchell, J.L.

1998-03-01

Nitric acid from plutonium process waste is a candidate for waste minimization by recycling. Process simulation software packages, such as Aspen, are valuable tools to estimate how effective recovery processes can be, however, constants in equations of state for many ionic components are not in their data libraries. One option is to combine single salt solubility`s in the Aspen model for mixed salt system. Single salt solubilities were regressed in Aspen within 0.82 weight percent of literature values. These were combined into a single Aspen model and used in the mixed salt studies. A simulated nitric acid waste containing mixed aluminum, calcium, iron, magnesium and sodium nitrate was tested to determine points of solubility between 25 and 100 C. Only four of the modeled experimental conditions, at 50 C and 75 C, produced a saturated solution. While experimental results indicate that sodium nitrate is the first salt to crystallize out, the Aspen computer model shows that the most insoluble salt, magnesium nitrate, the first salt to crystallize. Possible double salt formation is actually taking place under experimental conditions, which is not captured by the Aspen model.

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

International Nuclear Information System (INIS)

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

2007-01-01

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

Long term management of wastes contaminated by plutonium

International Nuclear Information System (INIS)

Marque, Y.

1983-01-01

For the different categories of wastes, the evolution of the cumulated production until the year 2000 is described by curves and the general situation of production points is presented, all that in France. The storage conditions are specified according to the type of wastes, category A, B, or C; the threshold under which the waste is classified in A category being fixed by the safety authorities at 2.10 4 CMA (maximum permissible concentration), that is to say for plutonium 1Ci/m 3 . The knowledge of waste activity is another basic element of the management of such wastes, the fixing of the threshold, above which wastes contaminated by plutonium have to be stored underground, still keeping to be specified [fr

Aqueous recovery of plutonium from pyrochemical processing residues

International Nuclear Information System (INIS)

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

1984-01-01

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

Technical support for GEIS: radioactive waste isolation in geologic formations. Volume 8. Repository preconceptual design studies: salt

International Nuclear Information System (INIS)

1978-04-01

This volume, Volume 8 ''Repository Preconceptual Design Studies: Salt,'' is one of a 23-volume series, ''Technical Support for GEIS: Radioactive Waste Isolation in Geologic Formations,'' Y/OWI/TM-36, which supplements the ''Contribution to Draft Generic Environmental Impact Statement on Commercial Waste Management: Radioactive Waste Isolation in Geologic Formations,'' Y/OWI/TM-44. The series provides a more complete technical basis for the preconceptual designs, resource requirements, and environmental source terms associated with isolating commercial LWR wastes in underground repositories in salt, granite, shale and basalt. Wastes are considered from three fuel cycles: uranium and plutonium recycling, no recycling of spent fuel and uranium-only recycling. This document describes a preconceptual design for a nuclear waste storage facility in salt. The facility design consists of several chambers excavated deep within a geologic formation together with access shafts and supportive surface structures. The facility design provides for: receiving and unloading waste containers; lowering them down shafts to the mine level; transporting them to the proper storage area, and emplacing them in mined storage rooms. Drawings of the facility design are contained in TM-36/9, ''Drawings for Repository Preconceptual Design Studies: Salt.''

Corrosive gas generation potential from chloride salt radiolysis in plutonium environments

International Nuclear Information System (INIS)

Tandon, L.; Allen, T.H.; Mason, R.E.; Penneman, R.A.

1999-01-01

The specific goal of this project was to evaluate the magnitude and practical significance of radiation effects involving mixtures of chloride salts and plutonium dioxide (PuO 2 ) sealed in stainless steel containers and stored for up to 50 yr, after stabilization at 950 C and packaging according to US Department of Energy (DOE) standards. The potential for generating chemically aggressive molecular chlorine (and hydrogen chloride by interaction with adsorbed water or hydrogen gas) by radiolysis of chloride ions was studied. To evaluate the risks, an annotated bibliography on chloride salt radiolysis was created with emphasis on effects of plutonium alpha radiation. The authors present data from the material identification and surveillance (MIS) project obtained from examination and analysis of representative PuO 2 items from various DOE sites, including the headspace gas analysis data of sealed mixtures of PuO 2 and chloride salts following long-term storage

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

International Nuclear Information System (INIS)

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

2004-01-01

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

Documentation of acceptable knowledge for LANL Plutonium Facility transuranic waste streams

International Nuclear Information System (INIS)

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

1998-01-01

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

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 techniques for measuring plutonium contents in TRU wastes by NDA methods

International Nuclear Information System (INIS)

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

1983-01-01

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

Removal of plutonium from real time waste using supercritical fluid extraction

International Nuclear Information System (INIS)

Sujatha, K.; Sivaraman, N.; Kumar, R.; Srinivasan, T.G.; Vasudeva Rao, P.R.

2010-01-01

Supercritical fluid extraction (SFE) technique was carried out for the recovery of plutonium from cellulose waste matrix using supercritical carbon dioxide (SC-CO 2 ) modified with suitable ligands such as octylphenyl N,N-diisobutyl carbamoylmethyl phosphine oxide (φCMPO), tri-n-butyl phosphate (TBP), acetyl acetone, trifluoro acetyl acetone and theonyltrifluoroacetyl acetone (TTA). The maximum plutonium recovery was found to be 99.8% when SC-CO 2 modified with CMPO was employed. About 15mg of plutonium was recovered from waste. (author)

Waste forms for plutonium disposition

International Nuclear Information System (INIS)

Johnson, S.G.; O'Holleran, T.P.; Frank, S.M.; Meyer, M.K.; Hanson, M.; Staples, B.A.; Knecht, D.A.; Kong, P.C.

1997-01-01

The field of plutonium disposition is varied and of much importance, since the Department of Energy has decided on the hybrid option for disposing of the weapons materials. This consists of either placing the Pu into mixed oxide fuel for reactors or placing the material into a stable waste form such as glass. The waste form used for Pu disposition should exhibit certain qualities: (1) provide for a suitable deterrent to guard against proliferation; (2) be of minimal volume, i.e., maximize the loading; and (3) be reasonably durable under repository-like conditions. This paper will discuss several Pu waste forms that display promising characteristics

Crystalline ceramics: Waste forms for the disposal of weapons plutonium

International Nuclear Information System (INIS)

Ewing, R.C.; Lutze, W.; Weber, W.J.

1995-05-01

At present, there are three seriously considered options for the disposition of excess weapons plutonium: (i) incorporation, partial burn-up and direct disposal of MOX-fuel; (ii) vitrification with defense waste and disposal as glass ''logs''; (iii) deep borehole disposal (National Academy of Sciences Report, 1994). The first two options provide a safeguard due to the high activity of fission products in the irradiated fuel and the defense waste. The latter option has only been examined in a preliminary manner, and the exact form of the plutonium has not been identified. In this paper, we review the potential for the immobilization of plutonium in highly durable crystalline ceramics apatite, pyrochlore, monazite and zircon. Based on available data, we propose zircon as the preferred crystalline ceramic for the permanent disposition of excess weapons plutonium

Volume reduction and plutonium recovery in alpha wastes by cryogenic crushing and lixiviation

International Nuclear Information System (INIS)

Arnal, T.; Pajot, J.

1986-06-01

The industry of plutonium generates solid alpha wastes of medium activity called ''technological wastes''. They are mainly produced during the fabrication and reprocessing of nuclear reactor fuels and they are of a wide variety i.e: vinyl bags, gloves, glass, steel materials used in glove box operation, etc... These wastes contain relevant residual quantities of uranium and plutonium in the form of oxides or nitrates, reaching up to several dozen grams per cubic meter. Up to the beginning of the eighties, they were conditionned without any treatment and stored as such on the production site. However, for an economic and safe storage, recovering of the plutonium contained in these waste streams and reduction of their volume is of obvious importance. At the plutonium ''Complexe de Fabrication des Combustibles de Cadarache'' was developed a new technical solution of this problem that combines cryogenic crushing of the solid waste and plutonium recovery from the crushed material by chemical lixiviation. The first results obtained in applying this system on the industrial scale are reported briefly

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

Liquid waste treatment at plutonium fuels fabrication facility, 2

International Nuclear Information System (INIS)

Matsumoto, Ken-ichi; Itoh, Ichiroh; Ohuchi, Jin; Miyo, Hiroaki

1974-01-01

The economics in the management of the radioactive liquid waste from Plutonium Fuels Fabrication Facility with sludge-blanket type flocculators has been evaluated. (1) Cost calculation: The cost of chemicals and electricity to treat 1 cubic meter of liquid waste is about 876 yen, while the total operating cost is 250 thousand yen per cubic meter in the case of 140 m 3 /year treatment. These figures are much higher than those for ordinary wastes, due to the particular operation against plutonium. (2) Proposal of the closed system for liquid waste treatment at PFFF: In the case of a closed system using evaporator, ion exchange column and rotary-kiln calciner, the operating cost is estimated at 40 thousand yen per cubic meter of liquid waste. Final radioactivity of treated liquid is below 10 -8 micro curies/ml. (Mori, K.)

Radiolytic and thermal stability of selected plutonium salts containing nitrate groups

International Nuclear Information System (INIS)

Bryan, G.H.

1976-04-01

(Pu(NO 3 ) 4 . XH 2 O, K 2 Pu(NO 3 ) 6 , and (NH 4 ) 2 Pu(NO 3 ) 6 ) were studied to evaluate their ability to serve as shipping forms that meet criteria. The radiolytic gas evolution study eliminated (NH 4 ) 2 Pu(NO 3 ) 6 from further consideration. None of the compounds produced H 2 or O 2 in sufficient quantity to produce a flammable mixture, except Pu(NO 3 ) 4 . XH 2 O which produced O 2 and H 2 in a ratio that is above explosive limits after long storage time. The ammonium salt decomposition appears to be about the same as that observed upon heating of NH 4 NO 3 to produce N 2 , H 2 O, and nitrous oxides. Plutonium nitrate contains hydration water. This water is of some concern due to the production of hydrogen by alpha-radiolysis. Two waters of hydration appear to be the lower limit to which Pu(NO 3 ) 4 . XH 2 O may be taken before decomposition of the solid begins. TGA results indicate the simple nitrate (Pu(NO 3 ) 4 . XH 2 O) is somewhat less thermally stable than either the ammonium or potassium hexanitrato plutonate which detracts somewhat from its suitability as a shipping form. Maintaining large quantities of this compound with a high 238 Pu content (less than 1 percent 238 Pu) may require specially designed and larger containers to prevent thermal degradation and gas pressure buildup problems. The informaion was presented to plutonium processors; the final consensus of this group was that in spite of some thermal instability of Pu(NO 3 ) 4 . XH 2 O at fairly low temperatures, it was preferable to K 2 Pu(NO 3 ) 6 due to the additional waste disposal problems the potassium would present. (Pu(NO 3 ) 4 . XH 2 O also has several other advantages. A possible problem that could arise due to the variable weight of plutonium nitrate could be in plutonium accountability, but this would be prevented if the plutonium content of the solution prior to evaporation to the solid is known

Materials considerations for molten salt accelerator-based plutonium conversion systems

International Nuclear Information System (INIS)

DiStefano, J.R.; DeVan, J.H.; Keiser, J.R.; Klueh, R.L.; Eatherly, W.P.

1995-03-01

Accelerator-driven transmutation technology (ADTT) refers to a concept for a system that uses a blanket assembly driven by a source of neutrons produced when high-energy protons from an accelerator strike a heavy metal target. One application for such a system is called Accelerator-Based Plutonium Conversion, or ABC. Currently, the version of this concept being proposed by the Los Alamos National Laboratory features a liquid lead target material and a blanket fuel of molten fluorides that contain plutonium. Thus, the materials to be used in such a system must have, in addition to adequate mechanical strength, corrosion resistance to molten lead, corrosion resistance to molten fluoride salts, and resistance to radiation damage. In this report the corrosion properties of liquid lead and the LiF-BeF 2 molten salt system are reviewed in the context of candidate materials for the above application. Background information has been drawn from extensive past studies. The system operating temperature, type of protective environment, and oxidation potential of the salt are shown to be critical design considerations. Factors such as the generation of fission products and transmutation of salt components also significantly affect corrosion behavior, and procedures for inhibiting their effects are discussed. In view of the potential for extreme conditions relative to neutron fluxes and energies that can occur in an ADTT, a knowledge of radiation effects is a most important factor. Present information for potential materials selections is summarized

Materials considerations for molten salt accelerator-based plutonium conversion systems

International Nuclear Information System (INIS)

DiStefano, J.R.; DeVan, J.H.; Keiser, J.R.; Klueh, R.L.; Eatherly, W.P.

1995-02-01

Accelerator-driven transmutation technology (ADTT) refers to a concept for a system that uses a blanket assembly driven by a source of neutrons produced when high-energy protons from an accelerator strike a heavy metal target. One application for such a system is called Accelerator-Based Plutonium Conversion, or ABC. Currently, the version of this concept being proposed by the Los Alamos National Laboratory features a liquid lead target material and a blanket fuel of molten fluorides that contain plutonium. Thus, the materials to be used in such a system must have, in addition to adequate mechanical strength, corrosion resistance to molten lead, corrosion resistance to molten fluoride salts, and resistance to radiation damage. In this report the corrosion properties of liquid lead and the LiF-BeF 2 molten salt system are reviewed in the context of candidate materials for the above application. Background information has been drawn from extensive past studies. The system operating temperature, type of protective environment, and oxidation potential of the salt are shown to be critical design considerations. Factors such as the generation of fission products and transmutation of salt components also significantly affect corrosion behavior, and procedures for inhibiting their effects are discussed. In view of the potential for extreme conditions relative to neutron fluxes and energies that can occur in an ADTT, a knowledge of radiation effects is a most important factor. Present information for potential materials selections is summarized

Study of interaction of uranium, plutonium and rare earth fluorides with some metal oxides in fluoric salt melts

International Nuclear Information System (INIS)

Gorbunov, V.F.; Novoselov, G.P.; Ulanov, S.A.

1976-01-01

Interaction of plutonium, uranium, and rare-earth elements (REE) fluorides with aluminium and calcium oxides in melts of eutectic mixture LiF-NaF has been studied at 800 deg C by X-ray diffraction method. It has been shown that tetravalent uranium and plutonium are coprecipitated by oxides as a solid solution UO 2 -PuO 2 . Trivalent plutonium in fluorides melts in not precipitated in the presence of tetravalent uranium which can be used for their separation. REE are precipitated from a salt melt by calcium oxide and are not precipitated by aluminium oxide. Thus, aluminium oxide in a selective precipitator for uranium and plutonium in presence of REE. Addition of aluminium fluoride retains trivalent plutonium and REE in a salt melt in presence of Ca and Al oxides. The mechanism of interacting plutonium and REE trifluorides with metal oxides in fluoride melts has been considered

Molten salt oxidation of organic hazardous waste with high salt content.

Science.gov (United States)

Lin, Chengqian; Chi, Yong; Jin, Yuqi; Jiang, Xuguang; Buekens, Alfons; Zhang, Qi; Chen, Jian

2018-02-01

Organic hazardous waste often contains some salt, owing to the widespread use of alkali salts during industrial manufacturing processes. These salts cause complications during the treatment of this type of waste. Molten salt oxidation is a flameless, robust thermal process, with inherent capability of destroying the organic constituents of wastes, while retaining the inorganic ingredients in the molten salt. In the present study, molten salt oxidation is employed for treating a typical organic hazardous waste with a high content of alkali salts. The hazardous waste derives from the production of thiotriazinone. Molten salt oxidation experiments have been conducted using a lab-scale molten salt oxidation reactor, and the emissions of CO, NO, SO 2 , HCl and dioxins are studied. Impacts are investigated from the composition of the molten salts, the types of feeding tube, the temperature of molten carbonates and the air factor. Results show that the waste can be oxidised effectively in a molten salt bath. Temperature of molten carbonates plays the most important role. With the temperature rising from 600 °C to 750 °C, the oxidation efficiency increases from 91.1% to 98.3%. Compared with the temperature, air factor has but a minor effect, as well as the composition of the molten salts and the type of feeding tube. The molten carbonates retain chlorine with an efficiency higher than 99.9% and the emissions of dioxins are below 8 pg TEQ g -1 sample. The present study shows that molten salt oxidation is a promising alternative for the disposal of organic hazardous wastes containing a high salt content.

Plutonium finishing plant dangerous waste training plan

International Nuclear Information System (INIS)

ENTROP, G.E.

1999-01-01

This training plan describes general requirements, worker categories, and provides course descriptions for operation of the Plutonium Finish Plant (PFP) waste generation facilities, permitted treatment, storage and disposal (TSD) units, and the 90-Day Accumulation Areas

Assay of plutonium contaminated waste by gamma spectrometry

International Nuclear Information System (INIS)

Adsley, I.; Bull, R.; Davies, M.; Green, M.

2011-01-01

The extreme toxicity of plutonium necessitates the segregation of plutonium contaminated materials (PCM) with extremely small (sub-μg) levels of contamination. The driver to measure accurately these small quantities of plutonium within (relatively) large volumes of waste is (in part) financial. In particular the cost of disposal (per unit volume) rises steeply with increasing waste-category. Within the UK, there has been a historical reluctance to use low energy gamma radiation to sentence PCM because of the potential for self attenuation by dense materials. This is unfortunate because the low-energy gamma radiation from PCM offers the only practicable technique for segregating PCM within the various Low Level Waste (LLW) (>0.4Bq/g) and sub-LLW categories. Whilst passive neutron counting techniques have proved successful for assay of waste well into the Intermediate Level Waste (ILW) (>100Bq/g) category, a cursory study reveals that these techniques are barely capable of detecting mg quantities of plutonium -- let alone the sub-μg quantities present in LLW. This paper considers the use of two types of gamma detector for assay of PCM: the thin sodium iodide FIDLER (Field Instrument for the Detection of Low Energy Radiation) and the HPGe (High Purity Germanium) detector. Systems utilising these two types of detector can provide complementary information. FIDLER measurements are conducted by careful, local, systematic monitoring of surfaces. By contrast a HPGe detector can be used to monitor entire walls, or even rooms, in one measurement. Thus, a HPGe detector placed in the centre of room (from which any radioactive hot-spots have previously been removed) could be used to demonstrate that the average activity remaining close to the surface of the walls/floor/ceiling is below a given limit. The Monte Carlo Code MCNP 1 has been used to model both FIDLER probe and HPGe detector in the measurement geometries described above. The MCNP simulations have been validated

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

Designing Advanced Ceramic Waste Forms for Electrochemical Processing Salt Waste

International Nuclear Information System (INIS)

Ebert, W. L.; Snyder, C. T.; Frank, Steven; Riley, Brian

2016-01-01

This report describes the scientific basis underlying the approach being followed to design and develop ''advanced'' glass-bonded sodalite ceramic waste form (ACWF) materials that can (1) accommodate higher salt waste loadings than the waste form developed in the 1990s for EBR-II waste salt and (2) provide greater flexibility for immobilizing extreme waste salt compositions. This is accomplished by using a binder glass having a much higher Na_2O content than glass compositions used previously to provide enough Na+ to react with all of the Cl- in the waste salt and generate the maximum amount of sodalite. The phase compositions and degradation behaviors of prototype ACWF products that were made using five new binder glass formulations and with 11-14 mass% representative LiCl/KCl-based salt waste were evaluated and compared with results of similar tests run with CWF products made using the original binder glass with 8 mass% of the same salt to demonstrate the approach and select a composition for further studies. About twice the amount of sodalite was generated in all ACWF materials and the microstructures and degradation behaviors confirmed our understanding of the reactions occurring during waste form production and the efficacy of the approach. However, the porosities of the resulting ACWF materials were higher than is desired. These results indicate the capacity of these ACWF waste forms to accommodate LiCl/KCl-based salt wastes becomes limited by porosity due to the low glass-to-sodalite volume ratio. Three of the new binder glass compositions were acceptable and there is no benefit to further increasing the Na content as initially planned. Instead, further studies are needed to develop and evaluate alternative production methods to decrease the porosity, such as by increasing the amount of binder glass in the formulation or by processing waste forms in a hot isostatic press. Increasing the amount of binder glass to eliminate porosity will decrease the waste

Designing Advanced Ceramic Waste Forms for Electrochemical Processing Salt Waste

Energy Technology Data Exchange (ETDEWEB)

Ebert, W. L. [Argonne National Lab. (ANL), Argonne, IL (United States); Snyder, C. T. [Argonne National Lab. (ANL), Argonne, IL (United States); Frank, Steven [Argonne National Lab. (ANL), Argonne, IL (United States); Riley, Brian [Argonne National Lab. (ANL), Argonne, IL (United States)

2016-03-01

This report describes the scientific basis underlying the approach being followed to design and develop “advanced” glass-bonded sodalite ceramic waste form (ACWF) materials that can (1) accommodate higher salt waste loadings than the waste form developed in the 1990s for EBR-II waste salt and (2) provide greater flexibility for immobilizing extreme waste salt compositions. This is accomplished by using a binder glass having a much higher Na₂O content than glass compositions used previously to provide enough Na+ to react with all of the Cl– in the waste salt and generate the maximum amount of sodalite. The phase compositions and degradation behaviors of prototype ACWF products that were made using five new binder glass formulations and with 11-14 mass% representative LiCl/KCl-based salt waste were evaluated and compared with results of similar tests run with CWF products made using the original binder glass with 8 mass% of the same salt to demonstrate the approach and select a composition for further studies. About twice the amount of sodalite was generated in all ACWF materials and the microstructures and degradation behaviors confirmed our understanding of the reactions occurring during waste form production and the efficacy of the approach. However, the porosities of the resulting ACWF materials were higher than is desired. These results indicate the capacity of these ACWF waste forms to accommodate LiCl/KCl-based salt wastes becomes limited by porosity due to the low glass-to-sodalite volume ratio. Three of the new binder glass compositions were acceptable and there is no benefit to further increasing the Na content as initially planned. Instead, further studies are needed to develop and evaluate alternative production methods to decrease the porosity, such as by increasing the amount of binder glass in the formulation or by processing waste forms in a hot isostatic press. Increasing the amount of binder glass to eliminate porosity will decrease

PLUTONIUM/HIGH-LEVEL VITRIFIED WASTE BDBE DOSE CALCULATION

Energy Technology Data Exchange (ETDEWEB)

J.A. Ziegler

2000-11-20

The purpose of this calculation is to provide a dose consequence analysis of high-level waste (HLW) consisting of plutonium immobilized in vitrified HLW to be handled at the proposed Monitored Geologic Repository at Yucca Mountain for a beyond design basis event (BDBE) under expected conditions using best estimate values for each calculation parameter. In addition to the dose calculation, a plutonium respirable particle size for dose calculation use is derived. The current concept for this waste form is plutonium disks enclosed in cans immobilized in canisters of vitrified HLW (i.e., glass). The plutonium inventory at risk used for this calculation is selected from Plutonium Immobilization Project Input for Yucca Mountain Total Systems Performance Assessment (Shaw 1999). The BDBE examined in this calculation is a nonmechanistic initiating event and the sequence of events that follow to cause a radiological release. This analysis will provide the radiological releases and dose consequences for a postulated BDBE. Results may be considered in other analyses to determine or modify the safety classification and quality assurance level of repository structures, systems, and components. This calculation uses best available technical information because the BDBE frequency is very low (i.e., less than 1.0E-6 events/year) and is not required for License Application for the Monitored Geologic Repository. The results of this calculation will not be used as part of a licensing or design basis.

Radiolytic gas generation in plutonium contaminated waste materials

International Nuclear Information System (INIS)

Kazanjian, A.R.

1976-01-01

Many plutonium contaminated waste materials decompose into gaseous products because of exposure to alpha radiation. The gases generated (usually hydrogen) over long-storage periods may create hazardous conditions. To determine the extent of such hazards, knowing the gas generation yields is necessary. These yields were measured by contacting some common Rocky Flats Plant waste materials with plutonium and monitoring the enclosed atmospheres for extensive periods of time. The materials were Plexiglas, polyvinyl chloride, glove-box gloves, machining oil, carbon tetrachloride, chlorothene VG solvent, Kimwipes (dry and wet), polyethylene, Dowex-1 resin, and surgeon's gloves. Both 239 Pu oxide and 238 Pu oxide were used as radiation sources. The gas analyses were made by mass spectrometry and the results obtained were the total gas generation, the hydrogen generation, the oxygen consumption rate, and the gas composition over the entire storage period. Hydrogen was the major gas produced in most of the materials. The total gas yields varied from 0.71 to 16 cm 3 (standard temperature pressure) per day per curie of plutonium. The oxygen consumption rates varied from 0.0088 to 0.070 millimoles per day per gram of plutonium oxide-239 and from 0.0014 to 0.0051 millimoles per day per milligram 238 Pu

Liquid waste processing from plutonium (III) oxalate precipitation

International Nuclear Information System (INIS)

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

1990-01-01

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

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

International Nuclear Information System (INIS)

Wilhite, E.L.

1978-08-01

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

Measurement of total alpha activity of neptunium, plutonium, and americium in highly radioactive Hanford waste by iron hydroxide precipitation and 2-heptanone solvent extraction

International Nuclear Information System (INIS)

Maiti, T.C.; Kaye, J.H.

1992-06-01

An improved method has been developed to concentrate the major alpha-emitting actinide elements neptunium, plutonium, and americium from samples with high salt content such as those resulting from efforts to characterize Hanford storage tank waste. Actinide elements are concentrated by coprecipitation of their hydroxides using iron carrier. The iron is removed by extraction from 8M HCI with 2-heptanone. The actinide elements remain in the aqueous phase free from salts, iron, and long-lived fission products. Recoveries averaged 98 percent

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

International Nuclear Information System (INIS)

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

2002-01-01

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

''FIXBOX'' - a new technique for the reliable conditioning of plutonium waste solutions

International Nuclear Information System (INIS)

Bruchertseifer, H.; Sommer, E.; Steinemann, M.; Bart, G.

1994-01-01

''FIXBOX'' - A new technique and facility for the conditioning of plutonium waste solutions has been developed and brought into operation in the Hot-laboratory at PSI, for the solidification of the waste from the research programmes. The facility is situated in glove-boxes for handling alpha activity and gamma-shielded for conditioning of fission product-containing waste. This report gives a brief description of the FIXBOX facility, the procedure and the first results of the cementation of plutonium waste solutions. As a result of this solidification, the actinide waste is homogeneous and strongly bound in the cement. The presence of gluconic acid and other complexing agents in the waste solution will not disturb this process. (author) figs., tabs., refs

Fully automated laboratory for the assay of plutonium in wastes and recoverable scraps

International Nuclear Information System (INIS)

Guiberteau, P.; Michaut, F.; Bergey, C.; Debruyne, T.

1990-01-01

To determine the plutonium content of wastes and recoverable scraps in intermediate size containers (ten liters) an automated laboratory has been carried out. Two passive methods of measurement are used. Gamma ray spectrometry allows plutonium isotopic analysis, americium determination and plutonium assay in wastes and poor scraps. Calorimetry is used for accurate (± 3%) plutonium determination in rich scraps. A full automation was realized with a barcode management and a supply robot to feed the eight assay set-ups. The laboratory works on a 24 hours per day and 365 days per year basis and has a capacity of 8,000 assays per year

Method of immobilizing weapons plutonium to provide a durable, disposable waste product

Science.gov (United States)

Ewing, Rodney C.; Lutze, Werner; Weber, William J.

1996-01-01

A method of atomic scale fixation and immobilization of plutonium to provide a durable waste product. Plutonium is provided in the form of either PuO.sub.2 or Pu(NO.sub.3).sub.4 and is mixed with and SiO.sub.2. The resulting mixture is cold pressed and then heated under pressure to form (Zr,Pu)SiO.sub.4 as the waste product.

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

International Nuclear Information System (INIS)

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

1986-01-01

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

Waste treatment using molten salt oxidation

International Nuclear Information System (INIS)

Navratil, J.D.; Stewart, A.E.

1996-01-01

MSO technology can be characterized as a submerged oxidation process; the basic concept is to introduce air and wastes into a bed of molten salt, oxidize the organic wastes in the molten salt, use the heat of oxidation to keep the salt molten and remove the salt for disposal or processing and recycling. The molten salt (usually sodium carbonate at 900-1000 C) provides four waste management functions: providing a heat transfer medium, catalyzing the oxidation reaction, preventing the formation of acid gases by forming stable salts, and efficiently capturing ash particles and radioactive materials by the combined effects of wetting, encapsulation and dissolution. The MSO process requires no wet scrubbing system for off-gas treatment. The process has been developed through bench-scale and pilot-scale testing, with successful destruction demonstration of a wide variety of hazardous and mixed (radioactive and hazardous wastes). (author). 24 refs, 2 tabs, 2 figs

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

International Nuclear Information System (INIS)

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

1998-03-01

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

Plutonium Finishing Plant (PFP) Treatment and Storage Unit Waste Analysis Plan

International Nuclear Information System (INIS)

PRIGNANO, A.L.

2000-01-01

The purpose of this waste analysis plan (WAP) is to document waste analysis activities associated with the Plutonium Finishing Plant Treatment and Storage Unit (PFP Treatment and Storage Unit) to comply with Washington Administrative Code (WAC) 173-303-300(1), (2), (4)(a) and (5). The PFP Treatment and Storage Unit is an interim status container management unit for plutonium bearing mixed waste radiologically managed as transuranic (TRU) waste. TRU mixed (TRUM) waste managed at the PFP Treatment and Storage Unit is destined for the Waste Isolation Pilot Plant (WIPP) and therefore is not subject to land disposal restrictions [WAC 173-303-140 and 40 CFR 268]. The PFP Treatment and Storage Unit is located in the 200 West Area of the Hanford Facility, Richland Washington (Figure 1). Because dangerous waste does not include source, special nuclear, and by-product material components of mixed waste, radionuclides are not within the scope of this documentation. The information on radionuclides is provided only for general knowledge

Plutonium assay of large waste burial containers at the Pacific Northwest Laboratory

International Nuclear Information System (INIS)

Haggard, D.L.; Newman, D.F.

1987-01-01

As one phase of an upgrade program at one of the Battelle Pacific Northwest Laboratory facilities, two plutonium glovebox hoods were replaced. They were dismantled, packaged in plastic for contamination control, and loaded into waste burial boxes. All of the plutonium-contaminated waste material from the two glovebox hoods was placed into six stainless steel boxes with identification letters A through F. Boxes A through E have 104.8- x 196.2- x 119.4-cm i.d.'s. Box F has an i.d. of 154.9 x 266.7 x 192.4 cm. The loaded boxes were assayed for plutonium content using both neutron and gamma-ray techniques. The difference between the results were greater than anticipated. Because of the importance of accurate plutonium assay measurements, additional measurements of box contents were made using a variety of techniques and assumptions including downloading of boxes and measurement of individual packages. These measurements have shown that a far-field, gamma-ray assay of a loaded waste box usually provides adequate measurement of low-density plutonium content, such as that found in packages of plastic, cellulose, and clothing. Comparing the far-field assays of the loaded waste boxes to the quantities determined by the assays of the downloaded packages resulted in good agreement between the two methods for boxes with low attenuation. Based on these results, it was concluded that it was valid to use the far-field assay results for the boxes that were not downloaded

Plutonium waste container identification

International Nuclear Information System (INIS)

Schmierer, T.J.

1979-01-01

The purpose of this paper is to define the parameters of a method for identifying plutonium waste containers. This information will form the basis for a permanent committee to develop a complete identification program for use throughout the world. Although a large portion of the information will be on handwritten notebooks and may not be as extensive as is desired, it will all be helpful. The final information will be programmed into computer language and be available to all interested parties as well as a central control committee which will have the expertise to provide each government with advice on the packaging, storage, and measurement of the waste for which it is responsible. As time progresses, this central control committee should develop permanent storage sites and establish a system of records which will last for hundreds of years

The management of plutonium (alpha) contaminated waste materials (PCM)

International Nuclear Information System (INIS)

Sills, R.J.

1984-01-01

This article reviews the management strategies for plutonium contaminated materials (PCM), the techniques which have been used and developed for their implementation and what can be expected for the immediate future. In general reference is made to the situation in the U.K., but where appropriate the International context is noted. In the context of the article plutonium often occurs with other alpha-active materials and the two terms are used virtually synonymously. The technology which is described, and which is the result of substantial research and development programmes, has largely been developed with the objective of recovering the majority of plutonium prior to ultimate disposal of the waste. There is no doubt that this removal to low levels of contamination is technically feasible; indeed there are a number of methods to choose from each with its own advantages and disadvantages. The emphasis has shifted recently from the development and demonstration of technology for waste handling, treatment and disposal (although these are very important), to the assessment of the effects--social, technological and economic--of the various options available for dealing with the waste. The process is thus, one of achieving the lowest overall 'cost' to society; where 'cost' is in the broadest sense of effect on society and not in merely strict financial terms

Plutonium metal preparation and purification at Los Alamos, 1984

International Nuclear Information System (INIS)

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

1984-01-01

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

An experimental study on Sodalite and SAP matrices for immobilization of spent chloride salt waste

Science.gov (United States)

Giacobbo, Francesca; Da Ros, Mirko; Macerata, Elena; Mariani, Mario; Giola, Marco; De Angelis, Giorgio; Capone, Mauro; Fedeli, Carlo

2018-02-01

In the frame of Generation IV reactors a renewed interest in pyro-processing of spent nuclear fuel is underway. Molten chloride salt waste arising from the recovering of uranium and plutonium through pyro-processing is one of the problematic wastes for direct application of vitrification or ceramization. In this work, Sodalite and SAP have been evaluated and compared as potential matrices for confinement of spent chloride salt waste coming from pyro-processing. To this aim Sodalite and SAP were synthesized both in pure form and mixed with different glass matrices, i.e. commercially available glass frit and borosilicate glass. The confining matrices were loaded with mixed chloride salts to study their retention capacities with respect to the elements of interest. The matrices were characterized and leached for contact times up to 150 days at room temperature and at 90 °C. SEM analyses were also performed in order to compare the matrix surface before and after leaching. Leaching results are discussed and compared in terms of normalized releases with similar results reported in literature. According to this comparative study the SAP matrix with glass frit binder resulted in the best matrix among the ones studied, with respect to retention capacities for both matrix and spent fuel elements.

Recovery of uranium and plutonium from Redox off-standard aqueous waste streams

Energy Technology Data Exchange (ETDEWEB)

Holm, C.H.; Matheson, A.R.

1949-12-31

In the operation of countercurrent extraction columns as in the Redox process, it is possible, and probable, that from unexpected behaviour of a column, operator error, colloid formation, etc., there will result from time to time excessive losses of uranium and plutonium in the overall process. These losses will naturally accumulate in the waste streams, particularly in the aqueous waste streams. If the loss is excessively high, and such lost material can be recovered by some additional method, then if economical and within reason, the recovered materials ran be returned to a ISF column for further processing. The objective of this work has been to develop such a method to recover uranium and plutonium from such off-standard waste streams in a form whereby the uranium send plutonium can be returned to the process line and subsequently purified and separated.

Waste Isolation Pilot Plant Salt Decontamination Testing

Energy Technology Data Exchange (ETDEWEB)

Rick Demmer; Stephen Reese

2014-09-01

On February 14, 2014, americium and plutonium contamination was released in the Waste Isolation Pilot Plant (WIPP) salt caverns. At the request of WIPP’s operations contractor, Idaho National Laboratory (INL) personnel developed several methods of decontaminating WIPP salt, using surrogate contaminants and also americium (241Am). The effectiveness of the methods is evaluated qualitatively, and to the extent possible, quantitatively. One of the requirements of this effort was delivering initial results and recommendations within a few weeks. That requirement, in combination with the limited scope of the project, made in-depth analysis impractical in some instances. Of the methods tested (dry brushing, vacuum cleaning, water washing, strippable coatings, and mechanical grinding), the most practical seems to be water washing. Effectiveness is very high, and it is very easy and rapid to deploy. The amount of wastewater produced (2 L/m2) would be substantial and may not be easy to manage, but the method is the clear winner from a usability perspective. Removable surface contamination levels (smear results) from the strippable coating and water washing coupons found no residual removable contamination. Thus, whatever is left is likely adhered to (or trapped within) the salt. The other option that shows promise is the use of a fixative barrier. Bartlett Nuclear, Inc.’s Polymeric Barrier System (PBS) proved the most durable of the coatings tested. The coatings were not tested for contaminant entrapment, only for coating integrity and durability.

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

Energy Technology Data Exchange (ETDEWEB)

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

1963-07-01

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

Bibliographical study for the development of an electrochemical preparation of plutonium molten salts; Etude bibliographique en vue de la mise au point d'une preparation electrochimique en sels fondus du plutonium

Energy Technology Data Exchange (ETDEWEB)

Lefevre, J.

1957-01-15

Based on an analogy with methods of electrochemical preparation of uranium molten salts, this bibliographical study reports data of physical properties of plutonium (melting point, density, ranges of existence of the different plutonium phases, resistivity, resistivity variation coefficient), discusses the search for an electrolytic bath (properties of plutonium bromides, chlorides and fluorides), and the required apparatus (an electrolysis cell)

Salt disposal of heat-generating nuclear waste

International Nuclear Information System (INIS)

Leigh, Christi D.; Hansen, Francis D.

2011-01-01

This report summarizes the state of salt repository science, reviews many of the technical issues pertaining to disposal of heat-generating nuclear waste in salt, and proposes several avenues for future science-based activities to further the technical basis for disposal in salt. There are extensive salt formations in the forty-eight contiguous states, and many of them may be worthy of consideration for nuclear waste disposal. The United States has extensive experience in salt repository sciences, including an operating facility for disposal of transuranic wastes. The scientific background for salt disposal including laboratory and field tests at ambient and elevated temperature, principles of salt behavior, potential for fracture damage and its mitigation, seal systems, chemical conditions, advanced modeling capabilities and near-future developments, performance assessment processes, and international collaboration are all discussed. The discussion of salt disposal issues is brought current, including a summary of recent international workshops dedicated to high-level waste disposal in salt. Lessons learned from Sandia National Laboratories' experience on the Waste Isolation Pilot Plant and the Yucca Mountain Project as well as related salt experience with the Strategic Petroleum Reserve are applied in this assessment. Disposal of heat-generating nuclear waste in a suitable salt formation is attractive because the material is essentially impermeable, self-sealing, and thermally conductive. Conditions are chemically beneficial, and a significant experience base exists in understanding this environment. Within the period of institutional control, overburden pressure will seal fractures and provide a repository setting that limits radionuclide movement. A salt repository could potentially achieve total containment, with no releases to the environment in undisturbed scenarios for as long as the region is geologically stable. Much of the experience gained from United

Salt disposal of heat-generating nuclear waste.

Energy Technology Data Exchange (ETDEWEB)

Leigh, Christi D. (Sandia National Laboratories, Carlsbad, NM); Hansen, Francis D.

2011-01-01

This report summarizes the state of salt repository science, reviews many of the technical issues pertaining to disposal of heat-generating nuclear waste in salt, and proposes several avenues for future science-based activities to further the technical basis for disposal in salt. There are extensive salt formations in the forty-eight contiguous states, and many of them may be worthy of consideration for nuclear waste disposal. The United States has extensive experience in salt repository sciences, including an operating facility for disposal of transuranic wastes. The scientific background for salt disposal including laboratory and field tests at ambient and elevated temperature, principles of salt behavior, potential for fracture damage and its mitigation, seal systems, chemical conditions, advanced modeling capabilities and near-future developments, performance assessment processes, and international collaboration are all discussed. The discussion of salt disposal issues is brought current, including a summary of recent international workshops dedicated to high-level waste disposal in salt. Lessons learned from Sandia National Laboratories' experience on the Waste Isolation Pilot Plant and the Yucca Mountain Project as well as related salt experience with the Strategic Petroleum Reserve are applied in this assessment. Disposal of heat-generating nuclear waste in a suitable salt formation is attractive because the material is essentially impermeable, self-sealing, and thermally conductive. Conditions are chemically beneficial, and a significant experience base exists in understanding this environment. Within the period of institutional control, overburden pressure will seal fractures and provide a repository setting that limits radionuclide movement. A salt repository could potentially achieve total containment, with no releases to the environment in undisturbed scenarios for as long as the region is geologically stable. Much of the experience gained from

Plutonium scrap waste processing based on aqueous nitrate and chloride media

International Nuclear Information System (INIS)

Navratil, J.D.

1985-01-01

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

The advantages of a salt/bentonite backfill for Waste Isolation Pilot Plant disposal rooms

International Nuclear Information System (INIS)

Butcher, B.M.; Novak, C.F.; Jercinovic, M.

1991-04-01

A 70/30 wt% salt/bentonite mixture is shown to be preferable to pure crushed salt as backfill for disposal rooms in the Waste Isolation Pilot Plant (WIPP). This report discusses several selection criteria used to arrive at this conclusion: the need for low permeability and porosity after closure, chemical stability with the surroundings, adequate strength to avoid shear erosion from human intrusion, ease of emplacement, and sorption potential for brine and radionuclides. Both salt and salt/bentonite are expected to consolidate to a final state of impermeability (i.e., ≤ 10 -18 m 2 ) adequate for satisfying federal nuclear regulations. Any advantage of the salt/bentonite mixture is dependent upon bentonite's potential for sorbing brine and radionuclides. Estimates suggest that bentonite's sorption potential for water in brine is much less than for pure water. While no credit is presently taken for brine sorption in salt/bentonite backfill, the possibility that some amount of inflowing brine would be chemically bound is considered likely. Bentonite may also sorb much of the plutonium, americium, and neptunium within the disposal room inventory. Sorption would be effective only if a major portion of the backfill is in contact with radioactive brine. Brine flow from the waste out through highly localized channels in the backfill would negate sorption effectiveness. Although the sorption potentials of bentonite for both brine and radionuclides are not ideal, they are distinctly beneficial. Furthermore, no detrimental aspects of adding bentonite to the salt as a backfill have been identified. These two observations are the major reasons for selecting salt/bentonite as a backfill within the WIPP. 39 refs., 16 figs., 6 tabs

Mixed Waste Salt Encapsulation Using Polysiloxane - Final Report

International Nuclear Information System (INIS)

Miller, C.M.; Loomis, G.G.; Prewett, S.W.

1997-01-01

A proof-of-concept experimental study was performed to investigate the use of Orbit Technologies polysiloxane grouting material for encapsulation of U.S. Department of Energy mixed waste salts leading to a final waste form for disposal. Evaporator pond salt residues and other salt-like material contaminated with both radioactive isotopes and hazardous components are ubiquitous in the DOE complex and may exceed 250,000,000 kg of material. Current treatment involves mixing low waste percentages (less than 10% by mass salt) with cement or costly thermal treatment followed by cementation to the ash residue. The proposed technology involves simple mixing of the granular salt material (with relatively high waste loadings-greater than 50%) in a polysiloxane-based system that polymerizes to form a silicon-based polymer material. This study involved a mixing study to determine optimum waste loadings and compressive strengths of the resultant monoliths. Following the mixing study, durability testing was performed on promising waste forms. Leaching studies including the accelerated leach test and the toxicity characteristic leaching procedure were also performed on a high nitrate salt waste form. In addition to this testing, the waste form was examined by scanning electron microscope. Preliminary cost estimates for applying this technology to the DOE complex mixed waste salt problem is also given

Equipping a glovebox for waste form testing and characterization of plutonium bearing materials

International Nuclear Information System (INIS)

Noy, M.; Johnson, S.G.; Moschetti, T.L.

1997-01-01

The recent decision by the Department of Energy to pursue a hybrid option for the disposition of weapons plutonium has created the need for additional facilities that can examine and characterize waste forms that contain Pu. This hybrid option consists of the placement of plutonium into stable waste forms and also into mixed oxide fuel for commercial reactors. Glass and glass-ceramic waste forms have a long history of being effective hosts for containing radionuclides, including plutonium. The types of tests necessary to characterize the performance of candidate waste forms include: static leaching experiments on both monolithic and crushed waste forms, microscopic examination, and density determination. Frequently, the respective candidate waste forms must first be produced using elevated temperatures and/or high pressures. The desired operations in the glovebox include, but are not limited to the following: (1) production of vitrified/sintered samples, (2) sampling of glass from crucibles or other vessels, (3) preparing samples for microscopic inspection and monolithic and crushed static leach tests, and (4) performing and analyzing leach tests in situ. This paper will describe the essential equipment and modifications that are necessary to successfully accomplish the goal of outfitting a glovebox for these functions

Developments in plutonium waste assay at AWE

International Nuclear Information System (INIS)

Miller, T J

2009-01-01

In 2002 a paper was presented at the 43rd Annual Meeting of the Institute of Nuclear Materials Management (INMM) on the assay of low level plutonium (Pu) in soft drummed waste (Miller 2002 INMM Ann. Meeting (Orlando, FL, 23-27 July 2002)). The technique described enabled the Atomic Weapons Establishment (AWE), at Aldermaston in the UK, to meet the stringent Low Level Waste Repository at Drigg (LLWRD) conditions for acceptance for the first time. However, it was initially applied to only low density waste streams because it relied on measuring the relatively low energy (60 keV) photon yield from Am-241 during growth. This paper reviews the results achieved when using the technique to assay over 10 000 waste packages and presents the case for extending the range of application to denser waste streams.

Recovery of plutonium from the combustion residues of alpha-bearing solid wastes

International Nuclear Information System (INIS)

Gompper, K.; Wieczorek, H.

1991-01-01

Experimental researches on plutonium dioxide dissolution in nitric acid in inactive and alpha-bearing wastes are presented in this report. After a review of the literature published on dissolution methods of PuO 2 combustion residues. Then results obtained in the ALONA plant on the dissolution of plutonium containing ashes in sulfuric acid and nitric acid are presented. Plutonium purification is studied. At last a simplified scheme of processing based on results obtained

Projected Salt Waste Production from a Commercial Pyroprocessing Facility

Directory of Open Access Journals (Sweden)

Michael F. Simpson

2013-01-01

Full Text Available Pyroprocessing of used nuclear fuel inevitably produces salt waste from electrorefining and/or oxide reduction unit operations. Various process design characteristics can affect the actual mass of such waste produced. This paper examines both oxide and metal fuel treatment, estimates the amount of salt waste generated, and assesses potential benefit of process options to mitigate the generation of salt waste. For reference purposes, a facility is considered in which 100 MT/year of fuel is processed. Salt waste estimates range from 8 to 20 MT/year from considering numerous scenarios. It appears that some benefit may be derived from advanced processes for separating fission products from molten salt waste, but the degree of improvement is limited. Waste form production is also considered but appears to be economically unfavorable. Direct disposal of salt into a salt basin type repository is found to be the most promising with respect to minimizing the impact of waste generation on the economic feasibility and sustainability of pyroprocessing.

Cementitious Stabilization of Mixed Wastes with High Salt Loadings

International Nuclear Information System (INIS)

Spence, R.D.; Burgess, M.W.; Fedorov, V.V.; Downing, D.J.

1999-01-01

Salt loadings approaching 50 wt % were tolerated in cementitious waste forms that still met leach and strength criteria, addressing a Technology Deficiency of low salt loadings previously identified by the Mixed Waste Focus Area. A statistical design quantified the effect of different stabilizing ingredients and salt loading on performance at lower loadings, allowing selection of the more effective ingredients for studying the higher salt loadings. In general, the final waste form needed to consist of 25 wt % of the dry stabilizing ingredients to meet the criteria used and 25 wt % water to form a workable paste, leaving 50 wt % for waste solids. The salt loading depends on the salt content of the waste solids but could be as high as 50 wt % if all the waste solids are salt

Radiation effects in glass waste forms for high-level waste and plutonium disposal

International Nuclear Information System (INIS)

Weber, W.J.; Ewing, R.C.

1997-01-01

A key challenge in the permanent disposal of high-level waste (HLW), plutonium residues/scraps, and excess weapons plutonium in glass waste forms is the development of predictive models of long-term performance that are based on a sound scientific understanding of relevant phenomena. Radiation effects from β-decay and α-decay can impact the performance of glasses for HLW and Pu disposition through the interactions of the α-particles, β-particles, recoil nuclei, and γ-rays with the atoms in the glass. Recently, a scientific panel convened under the auspices of the DOE Council on Materials Science to assess the current state of understanding, identify important scientific issues, and recommend directions for research in the area of radiation effects in glasses for HLW and Pu disposition. The overall finding of the panel was that there is a critical lack of systematic understanding on radiation effects in glasses at the atomic, microscopic, and macroscopic levels. The current state of understanding on radiation effects in glass waste forms and critical scientific issues are presented

Solubility of plutonium and waste evaporation

International Nuclear Information System (INIS)

Karraker, D.G.

1993-01-01

Chemical processing of irradiated reactor elements at the Savannah River Site separates uranium, plutonium and fission products; fission products and process-added chemicals are mixed with an excess of NaOH and discharged as a basic slurry into large underground tanks for temporary storage. The slurry is composed of base-insoluble solids that settle to the bottom of the tank; the liquid supemate contains a mixture of base-soluble chemicals--nitrates, nitrites aluminate, sulfate, etc. To conserve space in the waste tanks, the supemate is concentrated by evaporation. As the evaporation proceeds, the solubilities of some components are exceeded, and these species crystallize from solution. Normally, these components are soluble in the hot solution discharged from the waste tank evaporator and do not crystallize until the solution cools. However, concern was aroused at West Valley over the possibility that plutonium would precipitate and accumulate in the evaporator, conceivably to the point that a nuclear accident was possible. There is also a concern at SRS from evaporation of sludge washes, which arise from washing the base-insoluble solids (open-quote sludge close-quote) with ca. 1M NaOH to reduce the Al and S0 4 -2 content. The sludge washes of necessity extract a low level of Pu from the sludge and are evaporated to reduce their volume, presenting the possibility of precipitating Pu. Measurements of the solubility of Pu in synthetic solutions of similar composition to waste supernate and sludge washes are described in this report

Immobilization of chloride-rich radioactive wastes produced by pyrochemical operations

International Nuclear Information System (INIS)

McDaniel, E.W.; Terry, J.W.

1997-08-01

A a result of its former role as a producer of nuclear weapons components, the Rocky Flats Environmental Technology Site (RFETS), Golden, Colorado accumulated a variety of plutonium-contaminated materials. When the level of contamination exceeded a predetermined level (the economic discard limit), the materials were classified as residues rather than waste and were stored for later recovery of the plutonium. Although large quantities of residues were processed, others, primarily those more difficult to process, remain in storage at the site. It is planned for the residues with lower concentrations of plutonium to be disposed of as wastes at an appropriate disposal facility, probably the Waste Isolation Pilot Plant (WIPP). Because the plutonium concentration is too high or because the physical or chemical form would be difficult to get into a form acceptable to WIPP, it may not be possible to dispose of a portion of the residues at WIPP. The pyrochemical salts are among the residues that are difficult to dispose of. For a large percentage of the pyrochemical salts, safeguards controls are required, but WIPP was not designed to accommodate safeguards controls. A potential solution would be to immobilize the salts. These immobilized salts would contain substantially higher plutonium concentrations than is currently permissible but would be suitable for disposal at WIPP. This document presents the results of a review of three immobilization technologies to determine if mature technologies exist that would be suitable to immobilize pyrochemical salts: cement-based stabilization, low-temperature vitrification, and polymer encapsulation. The authors recommend that flow sheets and life-cycle costs be developed for cement-based and low-temperature glass immobilization

EVIDENCE OF CORROSIVE GAS FORMED BY RADIOLYSIS OF CHLORIDE SALTS IN PLUTONIUM-BEARING MATERIALS

Energy Technology Data Exchange (ETDEWEB)

Dunn, K.; Louthan, M.

2010-02-01

Corrosion and pitting have been observed in headspace regions of stainless steel containers enclosing plutonium oxide/salt mixtures. These observations are consistent with the formation of a corrosive gas, probably HCl, and transport of that gas to the headspace regions of sealed containers. The NH{sub 4}Cl films found on the walls of the sealed containers is also indicative of the presence of HCl gas. Radiolysis of hydrated alkaline earth salts is the probable source of HCl.

Alternatives for definse waste-salt disposal

International Nuclear Information System (INIS)

Benjamin, R.W.; McDonell, W.R.

1983-01-01

Alternatives for disposal of decontaminated high-level waste salt at Savannah River were reviewed to estimate costs and potential environmental impact for several processes. In this review, the reference process utilizing intermediate-depth burial of salt-concrete (saltcrete) monoliths was compared with alternatives including land application of the decontaminated salt as fertilizer for SRP pine stands, ocean disposal with and without containment, and terminal storage as saltcake in existing SRP waste tanks. Discounted total costs for the reference process and its modifications were in the same range as those for most of the alternative processes; uncontained ocean disposal with truck transport to Savannah River barges and storage as saltcake in SRP tanks had lower costs, but presented other difficulties. Environmental impacts could generally be maintained within acceptable limits for all processes except retention of saltcake in waste tanks, which could result in chemical contamination of surrounding areas on tank collapse. Land application would require additional salt decontamination to meet radioactive waste disposal standards, and ocean disposal without containment is not permitted in existing US practice. The reference process was judged to be the only salt disposal option studied which would meet all current requirements at an acceptable cost

Characterization of past and present solid waste streams from the plutonium finishing plant

Energy Technology Data Exchange (ETDEWEB)

Duncan, D.R.; Mayancsik, B.A. [Westinghouse Hanford Co., Richland, WA (United States); Pottmeyer, J.A.; Vejvoda, E.J.; Reddick, J.A.; Sheldon, K.M.; Weyns, M.I. [Los Alamos Technical Associates, Kennewick, WA (United States)

1993-02-01

During the next two decades the transuranic (TRU) wastes now stored in the burial trenches and storage facilities at the Hanford Site are to be retrieved, processed at the Waste Receiving and Processing (WRAP) Facility, and shipped to the Waste Isolation Pilot Plant (WIPP) near Carlsbad, New Mexico for final disposal. Over 50% of the TRU waste to be retrieved for shipment to the WIPP has been generated at the Plutonium Finishing Plant (PFP), also known as the Plutonium Processing and Storage Facility and Z Plant. The purpose of this report is to characterize the radioactive solid wastes generated by the PFP since its construction in 1947 using process knowledge, existing records, and history-obtained from interviews. The PFP is currently operated by Westinghouse Hanford Company (WHC) for the US Department of Energy (DOE).

Characterization of past and present solid waste streams from the plutonium finishing plant

International Nuclear Information System (INIS)

Duncan, D.R.; Mayancsik, B.A.; Pottmeyer, J.A.; Vejvoda, E.J.; Reddick, J.A.; Sheldon, K.M.; Weyns, M.I.

1993-02-01

During the next two decades the transuranic (TRU) wastes now stored in the burial trenches and storage facilities at the Hanford Site are to be retrieved, processed at the Waste Receiving and Processing (WRAP) Facility, and shipped to the Waste Isolation Pilot Plant (WIPP) near Carlsbad, New Mexico for final disposal. Over 50% of the TRU waste to be retrieved for shipment to the WIPP has been generated at the Plutonium Finishing Plant (PFP), also known as the Plutonium Processing and Storage Facility and Z Plant. The purpose of this report is to characterize the radioactive solid wastes generated by the PFP since its construction in 1947 using process knowledge, existing records, and history-obtained from interviews. The PFP is currently operated by Westinghouse Hanford Company (WHC) for the US Department of Energy (DOE)

Organic waste processing using molten salt oxidation

Energy Technology Data Exchange (ETDEWEB)

Adamson, M. G., LLNL

1998-03-01

Molten Salt Oxidation (MSO) is a thermal means of oxidizing (destroying) the organic constituents of mixed wastes, hazardous wastes, and energetic materials while retaining inorganic and radioactive constituents in the salt. For this reason, MSO is considered a promising alternative to incineration for the treatment of a variety of organic wastes. The U. S. Department of Energy`s Office of Environmental Management (DOE/EM) is currently funding research that will identify alternatives to incineration for the treatment of organic-based mixed wastes. (Mixed wastes are defined as waste streams which have both hazardous and radioactive properties.) One such project is Lawrence Livermore National Laboratory`s Expedited Technology Demonstration of Molten Salt Oxidation (MSO). The goal of this project is to conduct an integrated demonstration of MSO, including off-gas and spent salt treatment, and the preparation of robust solid final forms. Livermore National Laboratory (LLNL) has constructed an integrated pilot-scale MSO treatment system in which tests and demonstrations are presently being performed under carefully controlled (experimental) conditions. The system consists of a MSO process vessel with dedicated off-gas treatment, a salt recycle system, feed preparation equipment, and equipment for preparing ceramic final waste forms. In this paper we describe the integrated system and discuss its capabilities as well as preliminary process demonstration data. A primary purpose of these demonstrations is to identify the most suitable waste streams and waste types for MSO treatment.

Characterization of past and present solid waste streams from the Plutonium-Uranium Extraction Plant

International Nuclear Information System (INIS)

Pottmeyer, J.A.; Weyns, M.I.; Lorenzo, D.S.; Vejvoda, E.J.; Duncan, D.R.

1993-04-01

During the next two decades the transuranic wastes, now stored in the burial trenches and storage facilities at the Hanford Site, are to be retrieved, processed at the Waste Receiving and Processing Facility, and shipped to the Waste Isolation Pilot Plant near Carlsbad, New Mexico for final disposal. Over 7% of the transuranic waste to be retrieved for shipment to the Waste Isolation Pilot Plant has been generated at the Plutonium-Uranium Extraction (PUREX) Plant. The purpose of this report is to characterize the radioactive solid wastes generated by PUREX using process knowledge, existing records, and oral history interviews. The PUREX Plant is currently operated by the Westinghouse Hanford Company for the US Department of Energy and is now in standby status while being prepared for permanent shutdown. The PUREX Plant is a collection of facilities that has been used primarily to separate plutonium for nuclear weapons from spent fuel that had been irradiated in the Hanford Site's defense reactors. Originally designed to reprocess aluminum-clad uranium fuel, the plant was modified to reprocess zirconium alloy clad fuel elements from the Hanford Site's N Reactor. PUREX has provided plutonium for research reactor development, safety programs, and defense. In addition, the PUREX was used to recover slightly enriched uranium for recycling into fuel for use in reactors that generate electricity and plutonium. Section 2.0 provides further details of the PUREX's physical plant and its operations. The PUREX Plant functions that generate solid waste are as follows: processing operations, laboratory analyses and supporting activities. The types and estimated quantities of waste resulting from these activities are discussed in detail

Solubility of pllutonium in alkaline salt solutions

International Nuclear Information System (INIS)

Hobbs, D.T.; Edwards, T.B.

1993-01-01

Plutonium solubility data from several studies have been evaluated. For each data set, a predictive model has been developed where appropriate. In addition, a statistical model and corresponding prediction intervals for plutonium solubility as a quadratic function of the hydroxide concentration have been developed. Because of the wide range of solution compositions, the solubility of plutonium can vary by as much as three orders of magnitude for any given hydroxide concentration and still remain within the prediction interval. Any nuclear safety assessments that depend on the maximum amount of plutonium dissolved in alkaline salt solutions should use concentrations at least as great as the upper prediction limits developed in this study. To increase the confidence in the prediction model, it is recommended that additional solubility tests be conducted at low hydroxide concentrations and with all of the other solution components involved. To validate the model for application to actual waste solutions, it is recommended that the plutonium solubilities in actual waste solutions be determined and compared to the values predicted by the quadratic model

Determination by gamma-ray spectrometry of the plutonium and americium content of the Pu/Am separation scraps. Application to molten salts; Determination par spectrometrie gamma de la teneur en plutonium et en americium de produits issus de separation Pu/Am. Application aux bains de sels

Energy Technology Data Exchange (ETDEWEB)

Godot, A. [CEA Valduc, Dept. de Traitement des Materiaux Nucleaires, 21 - Is-sur-Tille (France); Perot, B. [CEA Cadarache, Dept. de Technologie Nucleaire, Service de Modelisation des Transferts et Mesures Nucleaires, 13 - Saint-Paul-lez-Durance (France)

2005-07-01

Within the framework of plutonium recycling operations in CEA Valduc (France), americium is extracted from molten plutonium metal into a molten salt during an electrolysis process. The scraps (spent salt, cathode, and crucible) contain extracted americium and a part of plutonium. Nuclear material management requires a very accurate determination of the plutonium content. Gamma-ray spectroscopy is performed on Molten Salt Extraction (MSE) scraps located inside the glove box, in order to assess the plutonium and americium contents. The measurement accuracy is influenced by the device geometry, nuclear instrumentation, screens located between the sample and the detector, counting statistics and matrix attenuation, self-absorption within the spent salt being very important. The purpose of this study is to validate the 'infinite energy extrapolation' method employed to correct for self-attenuation, and to detect any potential bias. We present a numerical study performed with the MCNP computer code to identify the most influential parameters and some suggestions to improve the measurement accuracy. A final uncertainty of approximately 40% is achieved on the plutonium mass. (authors)

Separation of uranium and common impurities from solid analytical waste containing plutonium

International Nuclear Information System (INIS)

Pathak, Nimai; Kumar, Mithlesh; Thulasidas, S.K.; Hon, N.S.; Kulkarni, M.J.; Mhatre, Amol; Natarajan, V.

2014-07-01

The report describes separation of uranium (U) and common impurities from solid analytical waste containing plutonium (Pu). This will be useful in recovery of Pu from nuclear waste. This is an important activity of any nuclear program in view of the strategic importance of Pu. In Radiochemistry Division, the trace metal analysis of Pu bearing fuel materials such as PuO 2 , (U,Pu)O 2 and (U,Pu)C are being carried out using the DC arc-Carrier Distillation technique. During these analyses, solid analytical waste containing Pu and 241 Am is generated. This comprises of left-over of samples and prepared charges. The main constituents of this waste are uranium oxide, plutonium oxide and silver chloride used as carrier. This report describes the entire work carried out to separate gram quantities of Pu from large amounts of U and mg quantities of 241 Am and the effect of leaching of the waste with nitric acid as a function of batch size. The effect of leaching the solid analytical waste of (U,Pu)O 2 and AgCl with concentrated nitric acid for different time intervals was also studied. Later keeping the time constant, the effect of nitric acid molarity on the leaching of U and Pu was investigated. Four different lots of the waste having different amounts were subjected to multiple leaching with 8 M nitric acid, each for 15 minutes duration. In all the experiments the amount of Uranium, Plutonium and other impurities leached were determined using ICP as an excitation source. The results are discussed in this report. (author)

Rapid screening method for plutonium in mixed waste samples

International Nuclear Information System (INIS)

Somers, W.; Culp, T.; Miller, R.

1987-01-01

A waste stream sampling program was undertaken to determine those waste streams which contained hazardous constituents, and would therefore be regulated as a hazardous waste under the Resource Conservation and Recovery Act. The waste streams also had the potential of containing radioactive material, either plutonium, americium, or depleted uranium. Because of the potential for contamination with radioactive material, a method of rapidly screening the liquid samples for radioactive material was required. A counting technique was devised to count a small aliquot of a sample, determine plutonium concentration, and allow the sample to be shipped the same day they were collected. This technique utilized the low energy photons (x-rays) that accompany α decay. This direct, non-destructive x-ray analysis was applied to quantitatively determine Pu-239 concentrations in industrial samples. Samples contained a Pu-239, Am-241 mixture; the ratio and/or concentrations of these two radionuclides was not constant. A computer program was designed and implemented to calculate Pu-239 activity and concentration (g/ml) using the 59.5 keV Am-241 peak to determine Am-241's contribution to the 17 keV region. Am's contribution was subtracted, yielding net counts in the 17 keV region due to Pu. 2 figs., 1 tab

Radionuclide compositions of spent fuel and high level waste for the uranium and plutonium fuelled PWR

International Nuclear Information System (INIS)

Fairclough, M.P.; Tymons, B.J.

1985-06-01

The activities of a selection of radionuclides are presented for three types of reactor fuel of interest in radioactive waste management. The fuel types are for a uranium 'burning' PWR, a plutonium 'burning' PWR using plutonium recycled from spent uranium fuel and a plutonium 'burning' PWR using plutonium which has undergone multiple recycle. (author)

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

International Nuclear Information System (INIS)

Gendre, R.

1962-01-01

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

Plutonium contaminated solid waste programs at the Los Alamos Scientific Laboratory

International Nuclear Information System (INIS)

Johson, L.J.; Jordan, H.S.

1975-01-01

Development of handling and storage criteria for plutonium contaminated solid waste materials is discussed. Data from corrosion and radiolytic attack studies are reviewed. Instrumentation systems developed for solid waste management applications at the 10nCi Pu/g waste material level is described and their sensitivity and operational limitations reviewed. Current programs for the environmental risk analysis of past waste disposal areas and for development of technology for the volume reduction and chemical stabilization of transuranic contaminated solid waste is outlined

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.

Is it possible to recycle nuclear wastes? Costs, risks and stakes of the plutonium industry

International Nuclear Information System (INIS)

2009-01-01

This document, published by the French association 'Sortir du nucleaire' (Get out of nuclear), gives some information on the chain reaction from uranium to plutonium, the difference between reprocessing (which does not reduce waste volumes but multiply waste types) and recycling, the high risks associated with plutonium transport, La Hague as the most dangerous nuclear site in France, reprocessing as the alibi for the French nuclear industry, Areva as an expert in propaganda, reprocessing as an absurd world strategy, plutonium as a fuel for proliferation, the myth of unlimited energy with the breeder reactors, and so on

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

Experience of management of plutonium-contaminated solid and liquid wastes at the Cadarache Nuclear Research Centre

International Nuclear Information System (INIS)

Marcaillou, J.; Faure, J.C.; Tourret, G.

1981-01-01

At Cadarache the principal sources of alpha-contaminated waste are the facilities of the plutonium fuel assembly fabrication complex. The chosen management scheme shows two points where it is possible to implement procedures to limit the activities released and to reduce the storage volumes of treated waste: (1) At the fabrication units, three categories of solid waste ('rich', 'poor' and 'special') are distinguished by sorting at the time of production and by γ,n counting of the drums. The rich and special wastes with a high plutonium content are stored while awaiting treatment for recycling of the plutonium. In the case of liquid waste, different circuits are used to separate contaminated effluents and thus to limit their production; (2) In the solid-waste treatment shops, the waste has so far been compacted and then coated with bituminous cement mortar. At the same time, a new incinerator facility has been installed. The preliminary studies dealt mainly with: waste preparation (crushing) to obtain a continuous and regular feed for the incinerator; combustion (pyrolysis followed by burning of the gases and unburnt matter in the presence of excess air); containment of the equipment. Further studies will be made to determine what is to be done with the ash (treatment for plutonium recovery and/or coating). At the Effluent Treatment Station some adjustments have had to be made in order to cope with the increase in volume activity due mainly to the presence of americium. At the same time, with a view to limiting the production of treatment residues with a high alpha-emitter content it has been decided to carry out a research and development programme on the separation of americium and the improvement of the recycling of the plutonium contained in the process effluents. (author)

Treatment studies of plutonium-bearing INEEL waste surrogates in a bench-scale arc furnace

International Nuclear Information System (INIS)

Freeman, C.J.

1997-05-01

Since 1989, the Subsurface Disposal Area (SDA) at the Idaho National Environmental and Engineering Laboratory (INEEL) has been included on the National Priority List for remediation. Arc- and plasma-heated furnaces are being considered for converting the radioactive mixed waste buried in the SDA to a stabilized-vitreous form. Nonradioactive, surrogate SDA wastes have been melted during tests in these types of furnaces, but data are needed on the behavior of transuranic (TRU) constituents, primarily plutonium, during thermal treatment. To begin collecting this data, plutonium-spiked SDA surrogates were processed in a bench-scale arc furnace to quantify the fate of the plutonium and other hazardous and nonhazardous metals. Test conditions included elevating the organic, lead, chloride, and sodium contents of the surrogates. Blends having higher organic contents caused furnace power levels to fluctuate. An organic content corresponding to 50% INEEL soil in a soil-waste blend was the highest achievable before power fluctuations made operating conditions unacceptable. The glass, metal, and off-gas solids produced from each surrogate blend tested were analyzed for elemental (including plutonium) content and the partitioning of each element to the corresponding phase was calculated

Treatment studies of plutonium-bearing INEEL waste surrogates in a bench-scale arc furnace

Energy Technology Data Exchange (ETDEWEB)

Freeman, C.J.

1997-05-01

Since 1989, the Subsurface Disposal Area (SDA) at the Idaho National Environmental and Engineering Laboratory (INEEL) has been included on the National Priority List for remediation. Arc- and plasma-heated furnaces are being considered for converting the radioactive mixed waste buried in the SDA to a stabilized-vitreous form. Nonradioactive, surrogate SDA wastes have been melted during tests in these types of furnaces, but data are needed on the behavior of transuranic (TRU) constituents, primarily plutonium, during thermal treatment. To begin collecting this data, plutonium-spiked SDA surrogates were processed in a bench-scale arc furnace to quantify the fate of the plutonium and other hazardous and nonhazardous metals. Test conditions included elevating the organic, lead, chloride, and sodium contents of the surrogates. Blends having higher organic contents caused furnace power levels to fluctuate. An organic content corresponding to 50% INEEL soil in a soil-waste blend was the highest achievable before power fluctuations made operating conditions unacceptable. The glass, metal, and off-gas solids produced from each surrogate blend tested were analyzed for elemental (including plutonium) content and the partitioning of each element to the corresponding phase was calculated.

Disposal of Savannah River Plant waste salt

International Nuclear Information System (INIS)

Dukes, M.D.

1982-01-01

Approximately 26-million gallons of soluble low-level waste salts will be produced during solidification of 6-million gallons of high-level defense waste in the proposed Defense Waste Processing Facility (DWPF) at the Savannah River Plant (SRP). Soluble wastes (primarily NaNO 3 , NaNO 2 , and NaOH) stored in the waste tanks will be decontaminated by ion exchange and solidified in concrete. The resulting salt-concrete mixture, saltcrete, will be placed in a landfill on the plantsite such that all applicable federal and state disposal criteria are met. Proposed NRC guidelines for the disposal of waste with the radionuclide content of SRP salt would permit shallow land burial. Federal and state rules require that potentially hazardous chemical wastes (mainly nitrate-nitrate salts in the saltcrete) be contained to the degree necessary to meet drinking water standards in the ground water beneath the landfill boundary. This paper describes the proposed saltcrete landfill and tests under way to ensure that the landfill will meet these criteria. The work includes laboratory and field tests of the saltcrete itself, a field test of a one-tenth linear scale model of the entire landfill system, and a numerical model of the system

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

International Nuclear Information System (INIS)

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

1979-05-01

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

Kinetics of the reduction of plutonium(IV) by hydroxyurea, a novel salt-free agent

International Nuclear Information System (INIS)

Zhu Zhaowu; He Jianyu; Zhang Zefu; Zhang Yu; Zheng Weifang

2004-01-01

The kinetics of the reduction of plutonium(IV) by hydroxyurea (HU), a novel salt free reductant, in nitric acid solutions has been studied. The observed reaction rate can be expressed as: -d[Pu(IV)]/dt=k 0 [Pu(IV)] 2 [HU]/[H + ] 0.9 , where k 0 = 5853 ± 363 (l 1.1 x mol -1.1 x s -1 ) at t = 13 deg C. The activation energy is about 81.2 kJ/mol. It was also shows that uranium(VI) has no appreciable influence on the reaction rate. Compared with other organic reductants our experiments indicate that HU is a very fast reductant for plutonium(IV). (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

Effect of using FLiBe and FLiNaBe molten salts bearing plutonium fluorides on the neutronic performance of PACER

International Nuclear Information System (INIS)

Acir, Adem

2012-01-01

In this paper, the effects of using FLiBe and FLiNaBe Molten Salts Bearing Plutonium Fluorides on the neutronic performance of the PACER are investigated. The optimum radial thickness for tritium self-sufficiency of the blankets addition of plutonium fluorides to FLiNaBe (LiF-/NaF BeF 2 ) and FLiBe (LiF-/BeF 2 ) of a dual purpose modified PACER concept are determined. The calculations are carried out with the one dimensional transport code XSDRNPM/SCALE5. The tritium breeding capacities of FLiNaBe and FLiBe with addition of plutonium fluorides in molten salt zone are investigated and compared. The optimum molten salt zone thickness is computed as 155 cm for tritium self-sufficiency of the blankets using FLiBe +1% PuF 4 whereas, the optimum thickness with FLiNaBe +1% PuF 4 is calculated as 170 cm. In addition, neutron transport calculations have been performed to evaluate the energy multiplication factor, total fission rate, displacement per atom and helium gas generation for optimal radial thickness in the blanket. Also, the tritium production and the radiation damage limits should be evaluated together in a fusion blanket for determining the optimum thickness of molten salt layer. (orig.)

Synthetic salt cake standards for analytical laboratory quality control

International Nuclear Information System (INIS)

Schilling, A.E.; Miller, A.G.

1980-01-01

The validation of analytical results in the characterization of Hanford Nuclear Defense Waste requires the preparation of synthetic waste for standard reference materials. Two independent synthetic salt cake standards have been prepared to monitor laboratory quality control for the chemical characterization of high-level salt cake and sludge waste in support of Rockwell Hanford Operations' High-Level Waste Management Program. Each synthetic salt cake standard contains 15 characterized chemical species and was subjected to an extensive verification/characterization program in two phases. Phase I consisted of an initial verification of each analyte in salt cake form in order to determine the current analytical capability for chemical analysis. Phase II consisted of a final characterization of those chemical species in solution form where conflicting verification data were observed. The 95 percent confidence interval on the mean for the following analytes within each standard is provided: sodium, nitrate, nitrite, phosphate, carbonate, sulfate, hydroxide, chromate, chloride, fluoride, aluminum, plutonium-239/240, strontium-90, cesium-137, and water

Possible combustion hazards in 3013 plutonium waste container

International Nuclear Information System (INIS)

Sherman, M.P.

1999-01-01

Are there combustion hazards in plutonium-contaminated waste containers caused by combustible gas generation? Current gas generation models in which the only reaction considered is radiolysis must inevitably predict eventual complete dissociation of any water present into hydrogen and oxygen. Waste prepared for the 3013 container should be less subject to this problem because organic material and most of the absorbed water should have been removed. Depending on the waste form, moisture content, organic content, temperature, and container material, the pressure rise due to gas generation will be bounded by backreactions, recombination of the hydrogen and oxygen, absorption of the oxygen by plutonium oxide, and possibly other chemical reactions. Examination of a variety of food pack waste containers at Los Alamos National Laboratory (LANL) has shown little pressure rise, indeed often subatmospheric pressures. In a few cases large hydrogen concentrations up to 47% mole fraction were observed, but with negligible oxygen content. The only fuel seen in significant quantities was H 2 and, in one case, CO; the only oxidizer seen in significant quantities was O 2 . Considerable work on measuring gas generation is being done at Westinghouse Savannah River Company and LANL. In a mixture of H 2 , O 2 , and other diluent gases, if the hydrogen concentration is below the value at the lean flammability limit, or if the oxygen concentration is below that at the rich flammability limit, a flame will not propagate from an ignition source. Assuming H 2 is the only fuel present in significant quantities, a mixture leaner than the lean limit will get only leaner if mixed with air and is therefore no combustion hazard. However, when a mixture containing large amounts of H 2 is nonflammable because there is insufficient O 2 , there is a hazard. If the mixture should leak into a volume containing O 2 , or the container is opened into the surrounding air, the mixture will pass through the

Fabrication of aluminum nitride crucibles for molten salt and plutonium compatibility studies

International Nuclear Information System (INIS)

Phillips, J.A.

1991-01-01

The overall objective of this research was to fabricate a calcium oxide sinter-aided aluminum nitride crucible and determine the compatibility of this crucible with molten chloride salts and plutonium metal in the DOR process. Calcium oxide sinter-aided aluminum nitride was preferred over yttrium oxide sinter-aided aluminum nitride because of (1) the presence of calcium chloride, calcium oxide, and calcium metal in the molten salts utilized in the DOR process, and (2) the higher volatility of the secondary phases formed compared with phases resulting from the addition of yttrium oxide during the aluminum nitride sintering process. The calcium oxide system may yield a higher purity crystal structure with fewer secondary phases present than in the yttrium oxide system. The secondary phases that are present in the grain boundaries may be unreactive with the calcium chloride salt due to the presence of calcium in the secondary phases

Solid waste disposal into salt mines

International Nuclear Information System (INIS)

Repke, W.

1981-01-01

The subject is discussed as follows: general introduction to disposal of radioactive waste; handling of solid nuclear waste; technology of final disposal, with specific reference to salt domes; conditioning of radioactive waste; safety barriers for radioactive waste; practice of final disposal in other countries. (U.K.)

Glass-Ceramic Waste Forms for Uranium and Plutonium Residues Wastes - 13164

International Nuclear Information System (INIS)

Stewart, Martin W.A.; Moricca, Sam A.; Zhang, Yingjie; Day, R. Arthur; Begg, Bruce D.; Scales, Charlie R.; Maddrell, Ewan R.; Hobbs, Jeff

2013-01-01

A program of work has been undertaken to treat plutonium-residues wastes at Sellafield. These have arisen from past fuel development work and are highly variable in both physical and chemical composition. The principal radiological elements present are U and Pu, with small amounts of Th. The waste packages contain Pu in amounts that are too low to be economically recycled as fuel and too high to be disposed of as lower level Pu contaminated material. NNL and ANSTO have developed full-ceramic and glass-ceramic waste forms in which hot-isostatic pressing is used as the consolidation step to safely immobilize the waste into a form suitable for long-term disposition. We discuss development work on the glass-ceramic developed for impure waste streams, in particular the effect of variations in the waste feed chemistry glass-ceramic. The waste chemistry was categorized into actinides, impurity cations, glass formers and anions. Variations of the relative amounts of these on the properties and chemistry of the waste form were investigated and the waste form was found to be largely unaffected by these changes. This work mainly discusses the initial trials with Th and U. Later trials with larger variations and work with Pu-doped samples further confirmed the flexibility of the glass-ceramic. (authors)

Integrated demonstration of molten salt oxidation with salt recycle for mixed waste treatment

International Nuclear Information System (INIS)

Hsu, P.C.

1997-01-01

Molten Salt Oxidation (MSO) is a thermal, nonflame process that has the inherent capability of completely destroying organic constituents of mixed wastes, hazardous wastes, and energetic materials while retaining inorganic and radioactive constituents in the salt. For this reason, MSO is considered a promising alternative to incineration for the treatment of a variety of organic wastes. Lawrence Livermore National Laboratory (LLNL) has prepared a facility and constructed an integrated pilot-scale MSO treatment system in which tests and demonstrations are performed under carefully controlled (experimental) conditions. The system consists of a MSO processor with dedicated off-gas treatment, a salt recycle system, feed preparation equipment, and equipment for preparing ceramic final waste forms. This integrated system was designed and engineered based on laboratory experience with a smaller engineering-scale reactor unit and extensive laboratory development on salt recycle and final forms preparation. In this paper we present design and engineering details of the system and discuss its capabilities as well as preliminary process demonstration data. A primary purpose of these demonstrations is identification of the most suitable waste streams and waste types for MSO treatment

Permanent Disposal of Nuclear Waste in Salt

Science.gov (United States)

Hansen, F. D.

2016-12-01

Salt formations hold promise for eternal removal of nuclear waste from our biosphere. Germany and the United States have ample salt formations for this purpose, ranging from flat-bedded formations to geologically mature dome structures. Both nations are revisiting nuclear waste disposal options, accompanied by extensive collaboration on applied salt repository research, design, and operation. Salt formations provide isolation while geotechnical barriers reestablish impermeability after waste is placed in the geology. Between excavation and closure, physical, mechanical, thermal, chemical, and hydrological processes ensue. Salt response over a range of stress and temperature has been characterized for decades. Research practices employ refined test techniques and controls, which improve parameter assessment for features of the constitutive models. Extraordinary computational capabilities require exacting understanding of laboratory measurements and objective interpretation of modeling results. A repository for heat-generative nuclear waste provides an engineering challenge beyond common experience. Long-term evolution of the underground setting is precluded from direct observation or measurement. Therefore, analogues and modeling predictions are necessary to establish enduring safety functions. A strong case for granular salt reconsolidation and a focused research agenda support salt repository concepts that include safety-by-design. Sandia National Laboratories is a multi-program laboratory managed and operated by Sandia Corporation, a wholly owned subsidiary of Lockheed Martin Corporation, for the U.S. Department of Energy's National Nuclear Security Administration under contract DE-AC04-94AL85000. Author: F. D. Hansen, Sandia National Laboratories

A combinatorial chemistry approach to the investigation of cerium oxide and plutonium oxide reactions with small molecules

Science.gov (United States)

Brady, John T.; Warner, Benjamin P.; Bridgewater, Jon S.; Havrilla, George J.; Morris, David E.; Buscher, C. Thomas

2000-07-01

We are currently investigating the potential chemistry of the 3013 Standard waste storage containers. These containers are filled with waste that is a mixture of inorganic salts and plutonium oxide that has been calcined to remove water and other volatiles. There has been concern about possible pressure buildup due to the formation of hydrogen or other gases. We are utilizing a combinatorial chemistry approach to investigate a range of possible reactions that may occur in the containers with various concentrations of metal oxides and inorganic salts.

Direct conversion of plutonium metal, scrap, residue, and transuranic waste to glass

International Nuclear Information System (INIS)

Forsberg, C.W.; Beahm, E.C.; Parker, G.W.; Malling, J.F.; Rudolph, J.

1995-01-01

A method for the direct conversion of metals, ceramics, organics, and amorphous solids to borosilicate glass has been invented. The process is called the Glass Material Oxidation and Dissolution System (GMODS). Traditional glass-making processes can convert only oxide materials to glass. However, many wastes contain complex mixtures of metals, ceramics, organics, and amorphous solids. Conversion of such mixtures to oxides followed by their conversion to glass is often impractical. GMODS may create a practical method to convert such mixtures to glass. Plutonium-containing materials (PCMS) exist in many forms, including metals, ceramics, organics, amorphous solids, and mixtures thereof. These PCMs vary from plutonium metal to filters made of metal, organic binders, and glass fibers. For storage and/or disposal of PCMS, it is desirable to convert PCMs to borosilicate glass. Borosilicate glass is the preferred repository waste form for high-level waste (HLW) because of its properties. PCMs converted to a transuranic borosilicate homogeneous glass would easily pass all waste acceptance and storage criteria. Conversion of PCMs to a glass would also simplify safeguards by conversion of heterogeneous PCMs to homogeneous glass. Thermodynamic calculations and proof-of-principle experiments on the GMODS process with cerium (plutonium surrogate), uranium, stainless steel, aluminum, Zircaloy-2, and carbon were successfully conducted. Initial analysis has identified potential flowsheets and equipment. Major unknowns remain, but the preliminary data suggests that GMODS may be a major new treatment option for PCMs

Advanced pyrochemical technologies for minimizing nuclear waste

International Nuclear Information System (INIS)

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

1994-01-01

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

Evolution Of Chemical Conditions And Estimated Plutonium Solubility In The Residual Waste Layer During Post-Closure Aging Of Tank 18

International Nuclear Information System (INIS)

Denham, M.

2012-01-01

This document updates the Eh-pH transitions from grout aging simulations and the plutonium waste release model of Denham (2007, Rev. 1) based on new data. New thermodynamic data for cementitious minerals are used for the grout simulations. Newer thermodynamic data, recommended by plutonium experts (Plutonium Solubility Peer Review Report, LA-UR-12-00079), are used to estimate solubilities of plutonium at various pore water compositions expected during grout aging. In addition, a new grout formula is used in the grout aging simulations and apparent solubilities of coprecipitated plutonium are estimated using data from analysis of Tank 18 residual waste. The conceptual model of waste release and the grout aging simulations are done in a manner similar to that of Denham (2007, Rev. 1). It is assumed that the pore fluid composition passing from the tank grout into the residual waste layer controls the solubility, and hence the waste release concentration of plutonium. Pore volumes of infiltrating fluid of an assumed composition are reacted with a hypothetical grout block using The Geochemist's Workbench(reg s ign) and changes in pore fluid chemistry correspond to the number of pore fluid volumes reacted. As in the earlier document, this results in three states of grout pore fluid composition throughout the simulation period that are termed Reduced Region II, Oxidized Region II, and Oxidized Region III. The one major difference from the earlier document is that pyrite is used to account for reducing capacity of the tank grout rather than pyrrhotite. This poises Eh at -0.47 volts during Reduced Region II. The major transitions in pore fluid composition are shown. Plutonium solubilities are estimated for discrete PuO2(am,hyd) particles and for plutonium coprecipitated with iron phases in the residual waste. Thermodynamic data for plutonium from the Nuclear Energy Agency are used to estimate the solubilities of the discrete particles for the three stages of pore fluid

Study on Utilization of Super Grade Plutonium in Molten Salt Reactor FUJI-U3 using CITATION Code

Science.gov (United States)

Wulandari, Cici; Waris, Abdul; Pramuditya, Syeilendra; Asril, Pramutadi AM; Novitrian

2017-07-01

FUJI-U3 type of Molten Salt Reactor (MSR) has a unique design since it consists of three core regions in order to avoid the replacement of graphite as moderator. MSR uses floride as a nuclear fuel salt with the most popular chemical composition is LiF-BeF2-ThF4-233UF4. ThF4 and 233UF4 are the fertile and fissile materials, respectively. On the other hand, LiF and BeF2 working as both fuel and heat transfer medium. In this study, the super grade plutonium will be utilized as substitution of 233U since plutonium is easier to be obtained compared to 233U as main fuel. Neutronics calculation was performed by using PIJ and CITATION modules of SRAC 2002 code with JENDL 3.2 as nuclear data library.

Roadmap for disposal of Electrorefiner Salt as Transuranic Waste.

Energy Technology Data Exchange (ETDEWEB)

Rechard, Robert P. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Trone, Janis R. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Kalinina, Elena Arkadievna [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Wang, Yifeng [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Hadgu, Teklu [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Sanchez, Lawrence C. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

2017-12-01

The experimental breeder reactor (EBR-II) used fuel with a layer of sodium surrounding the uranium-zirconium fuel to improve heat transfer. Disposing of EBR-II fuel in a geologic repository without treatment is not prudent because of the potentially energetic reaction of the sodium with water. In 2000, the US Department of Energy (DOE) decided to treat the sodium-bonded fuel with an electrorefiner (ER), which produces metallic uranium product, a metallic waste, mostly from the cladding, and the salt waste in the ER, which contains most of the actinides and fission products. Two waste forms were proposed for disposal in a mined repository; the metallic waste, which was to be cast into ingots, and the ER salt waste, which was to be further treated to produce a ceramic waste form. However, alternative disposal pathways for metallic and salt waste streams may reduce the complexity. For example, performance assessments show that geologic repositories can easily accommodate the ER salt waste without treating it to form a ceramic waste form. Because EBR-II was used for atomic energy defense activities, the treated waste likely meets the definition of transuranic waste. Hence, disposal at the Waste Isolation Pilot Plant (WIPP) in southern New Mexico, may be feasible. This report reviews the direct disposal pathway for ER salt waste and describes eleven tasks necessary for implementing disposal at WIPP, provided space is available, DOE decides to use this alternative disposal pathway in an updated environmental impact statement, and the State of New Mexico grants permission.

Calculation of keff for plutonium in high-level waste packages

International Nuclear Information System (INIS)

Zielinski, P.R.; Culbreth, W.G.

1994-01-01

The proposed national high-level nuclear waste repository will be designed to store approximately 70,000 tons of commercial spent fuel, but other forms of waste will also be considered for ultimate storage at this site. Plutonium in the form of PuO 2 may be added to borosilicate glass for ultimate disposal in the repository. The maximum amount of this fissile that may be added to a glass ''log'' will be limited by its ability to sustain a chain reaction. In this study, the removal of neutron absorbers from a glass log and the subsequent possibility of water infiltration were studied to find corresponding neutron multiplication factors. Weight fractions of 1%, 2%, and 3% PuO 2 were analyzed in the study. The results show the maximum amount of plutonium fissile that may be safely added to a glass log under conditions that lead to leaching of the principal neutron absorbers from the glass

Supplemental technical information in support of Y/OWI/TM--44. Volume 9. Drawings for repository preconceptual design studies: salt

International Nuclear Information System (INIS)

1978-04-01

Volume 9 contains drawings for a preconceptual design for a nuclear waste storage facility in salt. Drawings are included for three fuel cycles: fuel recycle, throwaway fuel cycle, and uranium recycle with plutonium in the high-level waste

Molten salt treatment to minimize and optimize waste

International Nuclear Information System (INIS)

Gat, U.; Crosley, S.M.; Gay, R.L.

1993-01-01

A combination molten salt oxidizer (MSO) and molten salt reactor (MSR) is described for treatment of waste. The MSO is proposed for contained oxidization of organic hazardous waste, for reduction of mass and volume of dilute waste by evaporation of the water. The NTSO residue is to be treated to optimize the waste in terms of its composition, chemical form, mixture, concentration, encapsulation, shape, size, and configuration. Accumulations and storage are minimized, shipments are sized for low risk. Actinides, fissile material, and long-lived isotopes are separated and completely burned or transmuted in an MSR. The MSR requires no fuel element fabrication, accepts the materials as salts in arbitrarily small quantities enhancing safety, security, and overall acceptability

Mixing Modeling Analysis For SRS Salt Waste Disposition

International Nuclear Information System (INIS)

Lee, S.

2011-01-01

Nuclear waste at Savannah River Site (SRS) waste tanks consists of three different types of waste forms. They are the lighter salt solutions referred to as supernate, the precipitated salts as salt cake, and heavier fine solids as sludge. The sludge is settled on the tank floor. About half of the residual waste radioactivity is contained in the sludge, which is only about 8 percentage of the total waste volume. Mixing study to be evaluated here for the Salt Disposition Integration (SDI) project focuses on supernate preparations in waste tanks prior to transfer to the Salt Waste Processing Facility (SWPF) feed tank. The methods to mix and blend the contents of the SRS blend tanks were evalutaed to ensure that the contents are properly blended before they are transferred from the blend tank such as Tank 50H to the SWPF feed tank. The work consists of two principal objectives to investigate two different pumps. One objective is to identify a suitable pumping arrangement that will adequately blend/mix two miscible liquids to obtain a uniform composition in the tank with a minimum level of sludge solid particulate in suspension. The other is to estimate the elevation in the tank at which the transfer pump inlet should be located where the solid concentration of the entrained fluid remains below the acceptance criterion (0.09 wt% or 1200 mg/liter) during transfer operation to the SWPF. Tank 50H is a Waste Tank that will be used to prepare batches of salt feed for SWPF. The salt feed must be a homogeneous solution satisfying the acceptance criterion of the solids entrainment during transfer operation. The work described here consists of two modeling areas. They are the mixing modeling analysis during miscible liquid blending operation, and the flow pattern analysis during transfer operation of the blended liquid. The modeling results will provide quantitative design and operation information during the mixing/blending process and the transfer operation of the blended

Continuous precipitation process of plutonium salts

International Nuclear Information System (INIS)

Richard, P.

1967-03-01

This work concerns the continuous precipitation process of plutonium oxalate. Investigations about the solubility of different valence states in nitric-oxalic and in nitric-sulfuric-oxalic medium lead to select the precipitation process of tetravalent plutonium oxalate. Settling velocity and granulometry of tetravalent oxalate plutonium have been studied with variation of several precipitation parameters such as: temperature, acidity, excess of oxalic acid and aging time. Then are given test results of some laboratory continuous apparatus. Conditions of operation with adopted tubular apparatus are defined in conclusion. A flow-sheet is given for a process at industrial scale. (author) [fr

Molten salt hazardous waste disposal process utilizing gas/liquid contact for salt recovery

International Nuclear Information System (INIS)

Grantham, L.F.; McKenzie, D.E.

1984-01-01

The products of a molten salt combustion of hazardous wastes are converted into a cooled gas, which can be filtered to remove hazardous particulate material, and a dry flowable mixture of salts, which can be recycled for use in the molten salt combustion, by means of gas/liquid contact between the gaseous products of combustion of the hazardous waste and a solution produced by quenching the spent melt from such molten salt combustion. The process results in maximizing the proportion of useful materials recovered from the molten salt combustion and minimizing the volume of material which must be discarded. In a preferred embodiment a spray dryer treatment is used to achieve the desired gas/liquid contact

Waste package designs for disposal of high-level waste in salt formations

International Nuclear Information System (INIS)

Basham, S.J. Jr.; Carr, J.A.

1984-01-01

In the United States of America the selected method for disposal of radioactive waste is mined repositories located in suitable geohydrological settings. Currently four types of host rocks are under consideration: tuff, basalt, crystalline rock and salt. Development of waste package designs for incorporation in mined salt repositories is discussed. The three pertinent high-level waste forms are: spent fuel, as disassembled and close-packed fuel pins in a mild steel canister; commercial high-level waste (CHLW), as borosilicate glass in stainless-steel canisters; defence high-level waste (DHLW), as borosilicate glass in stainless-steel canisters. The canisters are production and handling items only. They have no planned long-term isolation function. Each waste form requires a different approach in package design. However, the general geometry and the materials of the three designs are identical. The selected waste package design is an overpack of low carbon steel with a welded closure. This container surrounds the waste forms. Studies to better define brine quantity and composition, radiation effects on the salt and brines, long-term corrosion behaviour of the low carbon steel, and the leaching behaviour of the spent fuel and borosilicate glass waste forms are continuing. (author)

Geologic disposal of nuclear wastes: salt's lead is challenged

International Nuclear Information System (INIS)

Kerr, R.A.

1979-01-01

The types of radioactive waste disposal sites available are outlined. The use of salt deposits and their advantages are discussed. The reasons for the selection of the present site for the Waste Isolation Pilot Plant are presented. The possibilities of using salt domes along the Gulf Coast and not-salt rocks as nuclear waste repositories are also discussed. The sea bed characteristics are described and advantages of this type of site selection are presented

National Low-Level Waste Management Program Radionuclide Report Series, Volume 17: Plutonium-239

International Nuclear Information System (INIS)

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

1999-01-01

This report, Volume 17 of the National Low-Level Waste Management Program Radionuclide Report Series, discusses the radiological and chemical characteristics of plutonium-239 (Pu-239). This report also discusses waste types and forms in which Pu-239 can be found, waste and disposal information on Pu-239, and Pu-239 behavior in the environment and in the human body

National Low-Level Waste Management Program Radionuclide Report Series, Volume 17: Plutonium-239

Energy Technology Data Exchange (ETDEWEB)

J. P. Adams; M. L. Carboneau

1999-03-01

This report, Volume 17 of the National Low-Level Waste Management Program Radionuclide Report Series, discusses the radiological and chemical characteristics of plutonium-239 (Pu-239). This report also discusses waste types and forms in which Pu-239 can be found, waste and disposal information on Pu-239, and Pu-239 behavior in the environment and in the human body.

Characterization of transuranic solid wastes from a plutonium processing facility

International Nuclear Information System (INIS)

Mulkin, R.

1975-06-01

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

Expected environment for waste packages in a salt repository

International Nuclear Information System (INIS)

Pederson, L.R.; Clark, D.E.; Hodges, F.N.; McVay, G.L.; Rai, D.

1983-01-01

This paper discusses results of recent efforts to define the very near-field (within approximately 2 m) environmental conditions to which waste packages will be exposed in a salt repository. These conditions must be considered in the experimental design for waste package materials testing, which includes corrosion of barrier materials and leaching of waste forms. Site-specific brine compositions have been determined, and standard brine compositions have been selected for testing purposes. Actual brine compositions will vary depending on origin, temperature, irradiation history, and contact with irradiated rock salt. Results of irradiating rock salt, synthetic brines, rock salt/brine mixtures, and reactions of irradiated rock salt with brine solutions are reported. 38 references, 3 figures, 2 tables

Molten salt processing of mixed wastes with offgas condensation

International Nuclear Information System (INIS)

Cooper, J.F.; Brummond, W.; Celeste, J.; Farmer, J.; Hoenig, C.; Krikorian, O.H.; Upadhye, R.; Gay, R.L.; Stewart, A.; Yosim, S.

1991-01-01

We are developing an advanced process for treatment of mixed wastes in molten salt media at temperatures of 700--1000 degrees C. Waste destruction has been demonstrated in a single stage oxidation process, with destruction efficiencies above 99.9999% for many waste categories. The molten salt provides a heat transfer medium, prevents thermal surges, and functions as an in situ scrubber to transform the acid-gas forming components of the waste into neutral salts and immobilizes potentially fugitive materials by a combination of particle wetting, encapsulation and chemical dissolution and solvation. Because the offgas is collected and assayed before release, and wastes containing toxic and radioactive materials are treated while immobilized in a condensed phase, the process avoids the problems sometimes associated with incineration processes. We are studying a potentially improved modification of this process, which treats oxidizable wastes in two stages: pyrolysis followed by catalyzed molten salt oxidation of the pyrolysis gases at ca. 700 degrees C. 15 refs., 5 figs., 1 tab

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

Chloride-catalyzed corrosion of plutonium in glovebox atmospheres

International Nuclear Information System (INIS)

Burgess, M.; Haschke, J.M.; Allen, T.H.; Morales, L.A.; Jarboe, D.M.; Puglisi, C.V.

1998-04-01

Characterization of glovebox atmospheres and the black reaction product formed on plutonium surfaces shows that the abnormally rapid corrosion of components in the fabrication line is consistent with a complex salt-catalyzed reaction involving gaseous hydrogen chloride (HCl) and water. Analytical data verify that chlorocarbon and HCl vapors are presented in stagnant glovebox atmospheres. Hydrogen chloride concentrations approach 7 ppm at some locations in the glovebox line. The black corrosion product is identified as plutonium monoxide monohydride (PuOH), a product formed by hydrolysis of plutonium in liquid water and salt solutions at room temperature. Plutonium trichloride (PuCl 3 ) produced by reaction of HCl at the metal surface is deliquescent and apparently forms a highly concentrated salt solution by absorbing moisture from the glovebox atmosphere. Rapid corrosion is attributed to the ensuing salt-catalyzed reaction between plutonium and water. Experimental results are discussed, possible involvement of hydrogen fluoride (HF) is examined, and methods of corrective action are presented in this report

Solvent anode for plutonium purification

International Nuclear Information System (INIS)

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

1986-01-01

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

Provision of NDA instrumentation for the control of operations on plutonium finishing and waste plants at the Sellafield nuclear fuel reprocessing facility

International Nuclear Information System (INIS)

Whitehouse, K.R.; Orr, C.H.

1995-01-01

On BNFL's Sellafield site a significant number of major plants are involved in the handling, processing and storage of plutonium in various forms including nitrate, oxide and mixed oxide (MOX). Other plants in operation or under construction treat and prepare for storage, plutonium bearing wastes in the form of plutonium contaminated materials -- PCM (transuranic waste -- TRU) or low level waste. Concurrently, a number of old plutonium handling plants are being decommissioned. The safety and cost effectiveness of these widely varying operations has been ensured by the development and installation of a wide range of special radiometric instrumentation. These systems based on a range of neutron counting and high resolution gamma spectrometric techniques -- singly or in combination -- enable BNFL to maintain a detailed and comprehensive picture of the disposition of plutonium within each plant and across the site. This paper describes an overview of the range of plant and paper prove waste measurement systems in this context, highlighting the specific roles of the Plutonium Inventory Measurement System (PIMS) for real time accountancy and the Decommissioning In-Situ Plutonium Inventory Monitor (DISPIM) for material control during decommissioning

Estimate of the Sources of Plutonium-Containing Wastes Generated from MOX Fuel Production in Russia

International Nuclear Information System (INIS)

Kudinov, K. G.; Tretyakov, A. A.; Sorokin, Yu. P.; Bondin, V. V.; Manakova, L. F.; Jardine, L. J.

2002-01-01

In Russia, mixed oxide (MOX) fuel is produced in a pilot facility ''Paket'' at ''MAYAK'' Production Association. The Mining-Chemical Combine (MCC) has developed plans to design and build a dedicated industrial-scale plant to produce MOX fuel and fuel assemblies (FA) for VVER-1000 water reactors and the BN-600 fast-breeder reactor, which is pending an official Russian Federation (RF) site-selection decision. The design output of the plant is based on a production capacity of 2.75 tons of weapons plutonium per year to produce the resulting fuel assemblies: 1.25 tons for the BN-600 reactor FAs and the remaining 1.5 tons for VVER-1000 FAs. It is likely the quantity of BN-600 FAs will be reduced in actual practice. The process of nuclear disarmament frees a significant amount of weapons plutonium for other uses, which, if unutilized, represents a constant general threat. In France, Great Britain, Belgium, Russia, and Japan, reactor-grade plutonium is used in MOX-fuel production. Making MOX-fuel for CANDU (Canada) and pressurized water reactors (PWR) (Europe) is under consideration in Russia. If this latter production is added, as many as 5 tons of Pu per year might be processed into new FAs in Russia. Many years of work and experience are represented in the estimates of MOX fuel production wastes derived in this report. Prior engineering studies and sludge treatment investigations and comparisons have determined how best to treat Pu sludges and MOX fuel wastes. Based upon analyses of the production processes established by these efforts, we can estimate that there will be approximately 1200 kg of residual wastes subject to immobilization per MT of plutonium processed, of which approximately 6 to 7 kg is Pu in the residuals per MT of Pu processed. The wastes are various and complicated in composition. Because organic wastes constitute both the major portion of total waste and of the Pu to be immobilized, the recommended treatment of MOX-fuel production waste is

Estimate of the Sources of Plutonium-Containing Wastes Generated from MOX Fuel Production in Russia

Energy Technology Data Exchange (ETDEWEB)

Kudinov, K. G.; Tretyakov, A. A.; Sorokin, Yu. P.; Bondin, V. V.; Manakova, L. F.; Jardine, L. J.

2002-02-26

In Russia, mixed oxide (MOX) fuel is produced in a pilot facility ''Paket'' at ''MAYAK'' Production Association. The Mining-Chemical Combine (MCC) has developed plans to design and build a dedicated industrial-scale plant to produce MOX fuel and fuel assemblies (FA) for VVER-1000 water reactors and the BN-600 fast-breeder reactor, which is pending an official Russian Federation (RF) site-selection decision. The design output of the plant is based on a production capacity of 2.75 tons of weapons plutonium per year to produce the resulting fuel assemblies: 1.25 tons for the BN-600 reactor FAs and the remaining 1.5 tons for VVER-1000 FAs. It is likely the quantity of BN-600 FAs will be reduced in actual practice. The process of nuclear disarmament frees a significant amount of weapons plutonium for other uses, which, if unutilized, represents a constant general threat. In France, Great Britain, Belgium, Russia, and Japan, reactor-grade plutonium is used in MOX-fuel production. Making MOX-fuel for CANDU (Canada) and pressurized water reactors (PWR) (Europe) is under consideration in Russia. If this latter production is added, as many as 5 tons of Pu per year might be processed into new FAs in Russia. Many years of work and experience are represented in the estimates of MOX fuel production wastes derived in this report. Prior engineering studies and sludge treatment investigations and comparisons have determined how best to treat Pu sludges and MOX fuel wastes. Based upon analyses of the production processes established by these efforts, we can estimate that there will be approximately 1200 kg of residual wastes subject to immobilization per MT of plutonium processed, of which approximately 6 to 7 kg is Pu in the residuals per MT of Pu processed. The wastes are various and complicated in composition. Because organic wastes constitute both the major portion of total waste and of the Pu to be immobilized, the recommended treatment

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

Radioactive waste and special waste disposal in salt domes - phoney waste management solutions

International Nuclear Information System (INIS)

Grimmel, E.

1990-01-01

The paper tries to make aware of the fact that an indefinite safe disposal of anthropogeneous wastes in underground repositories is impossible. Suspicion is raised that the Gorleben-Rambow salt dome has never been studied for its suitability as a repository, but that it was simply taken for granted. Safety analyses are meant only to conceal uncertainty. It is demanded to immediately opt out of the ultimate disposal technique for radioactive and special wastes in salt caverns. (DG) [de

LLNL Site plan for a MOX fuel lead assembly mission in support of surplus plutonium disposition

Energy Technology Data Exchange (ETDEWEB)

Bronson, M.C.

1997-10-01

The principal facilities that LLNL would use to support a MOX Fuel Lead Assembly Mission are Building 332 and Building 334. Both of these buildings are within the security boundary known as the LLNL Superblock. Building 332 is the LLNL Plutonium Facility. As an operational plutonium facility, it has all the infrastructure and support services required for plutonium operations. The LLNL Plutonium Facility routinely handles kilogram quantities of plutonium and uranium. Currently, the building is limited to a plutonium inventory of 700 kilograms and a uranium inventory of 300 kilograms. Process rooms (excluding the vaults) are limited to an inventory of 20 kilograms per room. Ongoing operations include: receiving SSTS, material receipt, storage, metal machining and casting, welding, metal-to-oxide conversion, purification, molten salt operations, chlorination, oxide calcination, cold pressing and sintering, vitrification, encapsulation, chemical analysis, metallography and microprobe analysis, waste material processing, material accountability measurements, packaging, and material shipping. Building 334 is the Hardened Engineering Test Building. This building supports environmental and radiation measurements on encapsulated plutonium and uranium components. Other existing facilities that would be used to support a MOX Fuel Lead Assembly Mission include Building 335 for hardware receiving and storage and TRU and LLW waste storage and shipping facilities, and Building 331 or Building 241 for storage of depleted uranium.

LLNL Site plan for a MOX fuel lead assembly mission in support of surplus plutonium disposition

International Nuclear Information System (INIS)

Bronson, M.C.

1997-01-01

The principal facilities that LLNL would use to support a MOX Fuel Lead Assembly Mission are Building 332 and Building 334. Both of these buildings are within the security boundary known as the LLNL Superblock. Building 332 is the LLNL Plutonium Facility. As an operational plutonium facility, it has all the infrastructure and support services required for plutonium operations. The LLNL Plutonium Facility routinely handles kilogram quantities of plutonium and uranium. Currently, the building is limited to a plutonium inventory of 700 kilograms and a uranium inventory of 300 kilograms. Process rooms (excluding the vaults) are limited to an inventory of 20 kilograms per room. Ongoing operations include: receiving SSTS, material receipt, storage, metal machining and casting, welding, metal-to-oxide conversion, purification, molten salt operations, chlorination, oxide calcination, cold pressing and sintering, vitrification, encapsulation, chemical analysis, metallography and microprobe analysis, waste material processing, material accountability measurements, packaging, and material shipping. Building 334 is the Hardened Engineering Test Building. This building supports environmental and radiation measurements on encapsulated plutonium and uranium components. Other existing facilities that would be used to support a MOX Fuel Lead Assembly Mission include Building 335 for hardware receiving and storage and TRU and LLW waste storage and shipping facilities, and Building 331 or Building 241 for storage of depleted uranium

Transuranic (Tru) waste volume reduction operations at a plutonium facility

Energy Technology Data Exchange (ETDEWEB)

Cournoyer, Michael E [Los Alamos National Laboratory; Nixon, Archie E [Los Alamos National Laboratory; Dodge, Robert L [Los Alamos National Laboratory; Fife, Keith W [Los Alamos National Laboratory; Sandoval, Arnold M [Los Alamos National Laboratory; Garcia, Vincent E [Los Alamos National Laboratory

2010-01-01

Programmatic operations at the Los Alamos National Laboratory Plutonium Facility (TA 55) involve working with various amounts of plutonium and other highly toxic, alpha-emitting materials. The spread of radiological contamination on surfaces, airborne contamination, and excursions of contaminants into the operator's breathing zone are prevented through use of a variety of gloveboxes (the glovebox, coupled with an adequate negative pressure gradient, provides primary confinement). Size-reduction operations on glovebox equipment are a common activity when a process has been discontinued and the room is being modified to support a new customer. The Actin ide Processing Group at TA-55 uses one-meter-long glass columns to process plutonium. Disposal of used columns is a challenge, since they must be size-reduced to get them out of the glovebox. The task is a high-risk operation because the glass shards that are generated can puncture the bag-out bags, leather protectors, glovebox gloves, and the worker's skin when completing the task. One of the Lessons Learned from these operations is that Laboratory management should critically evaluate each hazard and provide more effective measures to prevent personnel injury. A bag made of puncture-resistant material was one of these enhanced controls. We have investigated the effectiveness of these bags and have found that they safely and effectively permit glass objects to be reduced to small pieces with a plastic or rubber mallet; the waste can then be easily poured into a container for removal from the glove box as non-compactable transuranic (TRU) waste. This size-reduction operation reduces solid TRU waste generation by almost 2% times. Replacing one-time-use bag-out bags with multiple-use glass crushing bags also contributes to reducing generated waste. In addition, significant costs from contamination, cleanup, and preparation of incident documentation are avoided. This effort contributes to the Los Alamos

Transuranic (Tru) waste volume reduction operations at a plutonium facility

International Nuclear Information System (INIS)

Cournoyer, Michael E.; Nixon, Archie E.; Dodge, Robert L.; Fife, Keith W.; Sandoval, Arnold M.; Garcia, Vincent E.

2010-01-01

Programmatic operations at the Los Alamos National Laboratory Plutonium Facility (TA 55) involve working with various amounts of plutonium and other highly toxic, alpha-emitting materials. The spread of radiological contamination on surfaces, airborne contamination, and excursions of contaminants into the operator's breathing zone are prevented through use of a variety of gloveboxes (the glovebox, coupled with an adequate negative pressure gradient, provides primary confinement). Size-reduction operations on glovebox equipment are a common activity when a process has been discontinued and the room is being modified to support a new customer. The Actin ide Processing Group at TA-55 uses one-meter-long glass columns to process plutonium. Disposal of used columns is a challenge, since they must be size-reduced to get them out of the glovebox. The task is a high-risk operation because the glass shards that are generated can puncture the bag-out bags, leather protectors, glovebox gloves, and the worker's skin when completing the task. One of the Lessons Learned from these operations is that Laboratory management should critically evaluate each hazard and provide more effective measures to prevent personnel injury. A bag made of puncture-resistant material was one of these enhanced controls. We have investigated the effectiveness of these bags and have found that they safely and effectively permit glass objects to be reduced to small pieces with a plastic or rubber mallet; the waste can then be easily poured into a container for removal from the glove box as non-compactable transuranic (TRU) waste. This size-reduction operation reduces solid TRU waste generation by almost 2% times. Replacing one-time-use bag-out bags with multiple-use glass crushing bags also contributes to reducing generated waste. In addition, significant costs from contamination, cleanup, and preparation of incident documentation are avoided. This effort contributes to the Los Alamos National

Transuranic (TRU) waste volume reduction operations at a plutonium facility

International Nuclear Information System (INIS)

Cournoyer, Michael E.; Nixon, Archie E.; Fife, Keith W.; Sandoval, Arnold M.; Garcia, Vincent E.; Dodge, Robert L.

2011-01-01

Programmatic operations at the Los Alamos National Laboratory Plutonium Facility (TA-55) involve working with various amounts of plutonium and other highly toxic, alpha-emitting materials. The spread of radiological contamination on surfaces, airborne contamination, and excursions of contaminants into the operator's breathing zone are prevented through use of a variety of gloveboxes (the glovebox, coupled with an adequate negative pressure gradient, provides primary confinement). Size-reduction operations on glovebox equipment are a common activity when a process has been discontinued and the room is being modified to support a new customer. The Actinide Processing Group at TA-55 uses one-meter or longer glass columns to process plutonium. Disposal of used columns is a challenge, since they must be size-reduced to get them out of the glovebox. The task is a high-risk operation because the glass shards that are generated can puncture the bag-out bags, leather protectors, glovebox gloves, and the worker's skin when completing the task. One of the Lessons Learned from these operations is that Laboratory management should critically evaluate each hazard and provide more effective measures to prevent personnel injury. A bag made of puncture-resistant material was one of these enhanced controls. We have investigated the effectiveness of these bags and have found that they safely and effectively permit glass objects to be reduced to small pieces with a plastic or rubber mallet; the waste can then be easily poured into a container for removal from the glovebox as non-compactable transuranic (TRU) waste. This size-reduction operation reduces solid TRU waste volume generation by almost 2½ times. Replacing one-time-use bag-out bags with multiple-use glass crushing bags also contributes to reducing generated waste. In addition, significant costs from contamination, cleanup, and preparation of incident documentation are avoided. This effort contributes to the Los Alamos

Microwave calcination for plutonium immobilization and residue stabilization

Energy Technology Data Exchange (ETDEWEB)

Harris, M.J.; Rising, T.L.; Roushey, W.J.; Sprenger, G.S. [Kaiser-Hill Co., Golden, CO (United States)

1995-12-01

In the late 1980`s development was begun on a process using microwave energy to vitrify low level mixed waste sludge and transuranic mixed waste sludge generated in Building 374 at Rocky Flats. This process was shown to produce a dense, highly durable waste form. With the cessation of weapons production at Rocky Flats, the emphasis has changed from treatment of low level and TRU wastes to stabilizaiton of plutonium oxide and residues. This equipment is versatile and can be used as a heat source to calcine, react or vitrify many types of residues and oxides. It has natural economies in that it heats only the material to be treated, significantly reducing cycle times over conventional furnaces. It is inexpensive to operate in that most of the working components remain outside of any necessary contamination enclosure and therefore can easily be maintained. Limited testing has been successfully performed on cerium oxide (as a surrogate for plutonium oxide), surrogate electrorefining salts, surrogate residue sludge and residue ash. Future plans also include tests on ion exchange resins. In an attempt to further the usefullness of this technology, a mobile, self-contained microwave melting system is currently under development and expected to be operational at Rocky Flats Enviromental Technology Site by the 4th quarter of FY96.

Microwave calcination for plutonium immobilization and residue stabilization

International Nuclear Information System (INIS)

Harris, M.J.; Rising, T.L.; Roushey, W.J.; Sprenger, G.S.

1995-01-01

In the late 1980's development was begun on a process using microwave energy to vitrify low level mixed waste sludge and transuranic mixed waste sludge generated in Building 374 at Rocky Flats. This process was shown to produce a dense, highly durable waste form. With the cessation of weapons production at Rocky Flats, the emphasis has changed from treatment of low level and TRU wastes to stabilizaiton of plutonium oxide and residues. This equipment is versatile and can be used as a heat source to calcine, react or vitrify many types of residues and oxides. It has natural economies in that it heats only the material to be treated, significantly reducing cycle times over conventional furnaces. It is inexpensive to operate in that most of the working components remain outside of any necessary contamination enclosure and therefore can easily be maintained. Limited testing has been successfully performed on cerium oxide (as a surrogate for plutonium oxide), surrogate electrorefining salts, surrogate residue sludge and residue ash. Future plans also include tests on ion exchange resins. In an attempt to further the usefullness of this technology, a mobile, self-contained microwave melting system is currently under development and expected to be operational at Rocky Flats Enviromental Technology Site by the 4th quarter of FY96

Membrane Treatment of Liquid Salt Bearing Radioactive Wastes

International Nuclear Information System (INIS)

Dmitriev, S. A.; Adamovich, D. V.; Demkin, V. I.; Timofeev, E. M.

2003-01-01

The main fields of introduction and application of membrane methods for preliminary treatment and processing salt liquid radioactive waste (SLRW) can be nuclear power stations (NPP) and enterprises on atomic submarines (AS) utilization. Unlike the earlier developed technology for the liquid salt bearing radioactive waste decontamination and concentrating this report presents the new enhanced membrane technology for the liquid salt bearing radioactive waste processing based on the state-of-the-art membrane unit design, namely, the filtering units equipped with the metal-ceramic membranes of ''TruMem'' brand, as well as the electrodialysis and electroosmosis concentrators. Application of the above mentioned units in conjunction with the pulse pole changer will allow the marked increase of the radioactive waste concentrating factor and the significant reduction of the waste volume intended for conversion into monolith and disposal. Besides, the application of the electrodialysis units loaded with an ion exchange material at the end polishing stage of the radioactive waste decontamination process will allow the reagent-free radioactive waste treatment that meets the standards set for the release of the decontaminated liquid radioactive waste effluents into the natural reservoirs of fish-farming value

Aqueous methods for recovery of plutonium from pyrochemical residues

International Nuclear Information System (INIS)

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

1987-01-01

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

Immobilization of IFR salt wastes in mortar

International Nuclear Information System (INIS)

Fischer, D.F.; Johnson, T.R.

1988-01-01

Portland cement-base mortars are being considered for immobilizing chloride salt wastes produced by the fuel cycles of Integral Fast Reactors (IFR). The IFR is a sodium-cooled fast reactor with metal alloy fuels. It has a close-coupled fuel cycle in which fission products are separated from the actinides in an electrochemical cell operating at 500/degree/C. This cell has a liquid cadmium anode in which the fuels are dissolved and a liquid salt electrolyte. The salt will be a mixture of either lithium, potassium, and sodium chlorides or lithium, calcium, barium, and sodium chlorides. One method being considered for immobilizing the treated nontransuranic salt waste is to disperse the salt in a portland cement-base mortar that will be sealed in corrosion-resistant containers. For this application, the grout must be sufficiently fluid that it can be pumped into canister-molds where it will solidify into a strong, leach-resistant material. The set times must be longer than a few hours to allow sufficient time for processing, and the mortar must reach a reasonable compressive strength (/approximately/7 MPa) within three days to permit handling. Because fission product heating will be high, about 0.6 W/kg for a mortar containing 10% waste salt, the effects of elevated temperatures during curing and storage on mortar properties must be considered

Shuffler calibration and measurement of mixtures of uranium and plutonium TRU-waste in a plant environment

International Nuclear Information System (INIS)

Hurd, J.R.

1998-01-01

The active-passive shuffler installed and certified a few years ago in Los Alamos National Laboratory's plutonium facility has now been calibrated for different matrices to measure Waste Isolation Pilot Plant (WIPP)-destined transuranic (TRU)-waste. Little or no data presently exist for these types of measurements in plant environments where there may be sudden large changes in the neutron background radiation which causes distortions in the results. Measurements and analyses of twenty-two 55-gallon drums, consisting of mixtures of varying quantities of uranium and plutonium, have been recently completed at the plutonium facility. The calibration and measurement techniques, including the method used to separate out the plutonium component, will be presented and discussed. Particular attention will be directed to those problems identified as arising from the plant environment. The results of studies to quantify the distortion effects in the data will be presented. Various solution scenarios will be indicated, along with those adopted here

Plutonium Finishing Plant Treatment and Storage Unit Dangerous Waste Training Plan

International Nuclear Information System (INIS)

ENTROP, G.E.

2000-01-01

The training program for personnel performing waste management duties pertaining to the Plutonium Finishing Plant (PFP) Treatment and Storage Unit is governed by the general requirements established in the Plutonium Finishing Plant Dangerous Waste Training Plan (PFP DWTP). The PFP Treatment and Storage Unit DWTP presented below incorporates all of the components of the PFP DWTP by reference. The discussion presented in this document identifies aspects of the training program specific to the PFP Treatment and Storage Unit. The training program includes specifications for personnel instruction through both classroom and on-the-job training. Training is developed specific to waste management duties. Hanford Facility personnel directly involved with the PFP Treatment and Storage Unit will receive training to container management practices, spill response, and emergency response. These will include, for example, training in the cementation process and training pertaining to applicable elements of WAC 173-303-330(1)(d). Applicable elements from WAC 173-303-330(1)(d) for the PFP Treatment and Storage Unit include: procedures for inspecting, repairing, and replacing facility emergency and monitoring equipment; communications and alarm systems; response to fires or explosions; and shutdown of operations

Qualitative and quantitative analysis of plutonium in solid waste drums

International Nuclear Information System (INIS)

Anno, Jacques; Escarieux, Emile

1977-01-01

An assessment of the results given by a study carried out for the development of qualitative and quantitative analysis, by γ spectrometry, of plutonium in solid waste drums is presented. After having reminded the standards and their incidence on the quantities of plutonium to be measured (application at industrial Pu: 20% of Pu 240 ) the equipment used is described. Measurement station provided with a mechanical system consisting of: a rail and a pulley block to bring the drums; a pit and a hydraulic jack with a rotating platform. The detection instrumentation consisting of: a high volume coaxial Ge(Li) detector with a γ ray resolution of 2 keV; an associated electronic; a processing of data by a 'Plurimat 20' minicomputer. Principles of the identification and measurements are specified and supported by experimental results. They are the following: determination of the quality of Pu by measuring the ratio between the γ ray intensities of the 239 Pu 129 keV and of the 241 Pu 148 keV; measurement of the 239 Pu mass by estimating the γ ray counting rate of the 375 keV from the calibrating curves given by plutonium samples varying from 32 mg to 80 g; correction of the results versus the source position into the drum and versus the filling in plastic materials into this drum. The experimental results obtained over 40 solid waste drums are presented along with the error estimates [fr

Estimation of Plutonium-240 Mass in Waste Tanks Using Ultra-Sensitive Detection of Radioactive Xenon Isotopes from Spontaneous Fission

Energy Technology Data Exchange (ETDEWEB)

Bowyer, Theodore W. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Gesh, Christopher J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Haas, Daniel A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Hayes, James C. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Johns, Jesse M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Lukins, Craig D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Mahoney, Lenna A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Meacham, Joseph E. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Mendoza, Donaldo P. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Olsen, Khris B. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Prinke, Amanda M. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Reid, Bruce D. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Sevigny, Gary J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Sinkov, Sergey I. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Woods, Vincent T. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2017-05-24

This report details efforts to develop a technique which is able to detect and quantify the mass of ²⁴⁰Pu in waste storage tanks and other enclosed spaces. If the isotopic ratios of the plutonium contained in the enclosed space is also known, then this technique is capable of estimating the total mass of the plutonium without physical sample retrieval and radiochemical analysis of hazardous material. Results utilizing this technique are reported for a Hanford Site waste tank (TX-118) and a well-characterized plutonium sample in a laboratory environment.

Treatment of waste salts by oxygen sparging and vacuum distillation

International Nuclear Information System (INIS)

Cho, Y.J.; Yang, H.C.; Kim, E.H.; Kin, I.T.; Eun, H.C.

2007-01-01

Full text of publication follows. During the electrorefining process of the oxide spent fuel from LWR, amounts of waste salts containing some metal chloride species such as rare earths and actinide chlorides are generated, where the reuse of the waste salts is very important from the standpoint of an economical as well as an environmental aspect. In order to reuse the waste salts, a salt vacuum distillation method can be used. For the best separation by a vacuum distillation, the metal chloride species involved in the waste salts must be converted into their oxide(or oxychloride) forms due to the their low volatility compared to that of LiCl-KCl. In this study, an oxygen sparging process was adopted for the oxidation (or precipitation) of rare earth chlorides. The effects of oxygen flow rate and molten salt temperature on the conversion of rare earth chlorides to the precipitate phase (i.e. oxide or oxychloride) were investigated. In addition, distillation characteristics of LiCl-KCl molten salt with system pressure and temperature were studied. (authors)

The use of curium neutrons to verify plutonium in spent fuel and reprocessing wastes

International Nuclear Information System (INIS)

Miura, N.

1994-05-01

For safeguards verification of spent fuel, leached hulls, and reprocessing wastes, it is necessary to determine the plutonium content in these items. We have evaluated the use of passive neutron multiplicity counting to determine the plutonium content directly and also to measure the 240 Pu/ 244 Cm ratio for the indirect verification of the plutonium. Neutron multiplicity counting of the singles, doubles, and triples neutrons has been evaluated for measuring 240 Pu, 244 Cm, and 252 Cf. We have proposed a method to establish the plutonium to curium ratio using the hybrid k-edge densitometer x-ray fluorescence instrument plus a neutron coincidence counter for the reprocessing dissolver solution. This report presents the concepts, experimental results, and error estimates for typical spent fuel applications

Salt removal from tanks containing high-level radioactive waste

International Nuclear Information System (INIS)

Kiser, D.L.

1981-01-01

At the Savannah River Plant (SRP), there are 23 waste storage tanks containing high-level radioactive wastes that are to be retired. These tanks contain about 23 million liters of salt and about 10 million liters of sludge, that are to be relocated to new Type III, fully stress-relieved tanks with complete secondary containment. About 19 million liters of salt cake are to be dissolved. Steam jet circulators were originally proposed for the salt dissolution program. However, use of steam jet circulators raised the temperature of the tank contents and caused operating problems. These included increased corrosion risk and required long cooldown periods prior to transfer. Alternative dissolution concepts were investigated. Examination of mechanisms affecting salt dissolution showed that the ability of fresh water to contact the cake surface was the most significant factor influencing dissolution rate. Density driven and mechanical agitation techniques were developed on a bench scale and then were demonstrated in an actual waste tank. Actual waste tank demonstrations were in good agreement with bench-scale experiments at 1/85 scale. The density driven method utilizes simple equipment, but leaves a cake heel in the tank and is hindered by the presence of sludge or Zeolite in the salt cake. Mechanical agitation overcomes the problems found with both steam jet circulators and the density driven technique and is the best method for future waste tank salt removal

Recovery of 238PuO2 by Molten Salt Oxidation Processing of 238PuO2 Contaminated Combustibles (Part II)

Science.gov (United States)

Remerowski, Mary Lynn; Dozhier, C.; Krenek, K.; VanPelt, C. E.; Reimus, M. A.; Spengler, D.; Matonic, J.; Garcia, L.; Rios, E.; Sandoval, F.; Herman, D.; Hart, R.; Ewing, B.; Lovato, M.; Romero, J. P.

2005-02-01

Pu-238 heat sources are used to fuel radioisotope thermoelectric generators (RTG) used in space missions. The demand for this fuel is increasing, yet there are currently no domestic sources of this material. Much of the fuel is material reprocessed from other sources. One rich source of Pu-238 residual material is that from contaminated combustible materials, such as cheesecloth, ion exchange resins and plastics. From both waste minimization and production efficiency standpoints, the best solution is to recover this material. One way to accomplish separation of the organic component from these residues is a flameless oxidation process using molten salt as the matrix for the breakdown of the organic to carbon dioxide and water. The plutonium is retained in the salt, and can be recovered by dissolution of the carbonate salt in an aqueous solution, leaving the insoluble oxide behind. Further aqueous scrap recovery processing is used to purify the plutonium oxide. Recovery of the plutonium from contaminated combustibles achieves two important goals. First, it increases the inventory of Pu-238 available for heat source fabrication. Second, it is a significant waste minimization process. Because of its thermal activity (0.567 W per gram), combustibles must be packaged for disposition with much lower amounts of Pu-238 per drum than other waste types. Specifically, cheesecloth residues in the form of pyrolyzed ash (for stabilization) are being stored for eventual recovery of the plutonium.

Recovery of 238PuO2 by Molten Salt Oxidation Processing of 238PuO2 Contaminated Combustibles (Part II)

International Nuclear Information System (INIS)

Remerowski, Mary Lynn; Dozhier, C.; Krenek, K.; VanPelt, C. E.; Reimus, M. A.; Spengler, D.; Matonic, J.; Garcia, L.; Rios, E.; Sandoval, F.; Herman, D.; Hart, R.; Ewing, B.; Lovato, M.; Romero, J. P.

2005-01-01

Pu-238 heat sources are used to fuel radioisotope thermoelectric generators (RTG) used in space missions. The demand for this fuel is increasing, yet there are currently no domestic sources of this material. Much of the fuel is material reprocessed from other sources. One rich source of Pu-238 residual material is that from contaminated combustible materials, such as cheesecloth, ion exchange resins and plastics. From both waste minimization and production efficiency standpoints, the best solution is to recover this material. One way to accomplish separation of the organic component from these residues is a flameless oxidation process using molten salt as the matrix for the breakdown of the organic to carbon dioxide and water. The plutonium is retained in the salt, and can be recovered by dissolution of the carbonate salt in an aqueous solution, leaving the insoluble oxide behind. Further aqueous scrap recovery processing is used to purify the plutonium oxide. Recovery of the plutonium from contaminated combustibles achieves two important goals. First, it increases the inventory of Pu-238 available for heat source fabrication. Second, it is a significant waste minimization process. Because of its thermal activity (0.567 W per gram), combustibles must be packaged for disposition with much lower amounts of Pu-238 per drum than other waste types. Specifically, cheesecloth residues in the form of pyrolyzed ash (for stabilization) are being stored for eventual recovery of the plutonium

Risk assessment of nonhazardous oil-field waste disposal in salt caverns.

Energy Technology Data Exchange (ETDEWEB)

Elcock, D.

1998-03-10

Salt caverns can be formed in underground salt formations incidentally as a result of mining or intentionally to create underground chambers for product storage or waste disposal. For more than 50 years, salt caverns have been used to store hydrocarbon products. Recently, concerns over the costs and environmental effects of land disposal and incineration have sparked interest in using salt caverns for waste disposal. Countries using or considering using salt caverns for waste disposal include Canada (oil-production wastes), Mexico (purged sulfates from salt evaporators), Germany (contaminated soils and ashes), the United Kingdom (organic residues), and the Netherlands (brine purification wastes). In the US, industry and the regulatory community are pursuing the use of salt caverns for disposal of oil-field wastes. In 1988, the US Environmental Protection Agency (EPA) issued a regulatory determination exempting wastes generated during oil and gas exploration and production (oil-field wastes) from federal hazardous waste regulations--even though such wastes may contain hazardous constituents. At the same time, EPA urged states to tighten their oil-field waste management regulations. The resulting restrictions have generated industry interest in the use of salt caverns for potentially economical and environmentally safe oil-field waste disposal. Before the practice can be implemented commercially, however, regulators need assurance that disposing of oil-field wastes in salt caverns is technically and legally feasible and that potential health effects associated with the practice are acceptable. In 1996, Argonne National Laboratory (ANL) conducted a preliminary technical and legal evaluation of disposing of nonhazardous oil-field wastes (NOW) into salt caverns. It investigated regulatory issues; the types of oil-field wastes suitable for cavern disposal; cavern design and location considerations; and disposal operations, closure and remediation issues. It determined

Risk assessment of nonhazardous oil-field waste disposal in salt caverns

International Nuclear Information System (INIS)

Elcock, D.

1998-01-01

Salt caverns can be formed in underground salt formations incidentally as a result of mining or intentionally to create underground chambers for product storage or waste disposal. For more than 50 years, salt caverns have been used to store hydrocarbon products. Recently, concerns over the costs and environmental effects of land disposal and incineration have sparked interest in using salt caverns for waste disposal. Countries using or considering using salt caverns for waste disposal include Canada (oil-production wastes), Mexico (purged sulfates from salt evaporators), Germany (contaminated soils and ashes), the United Kingdom (organic residues), and the Netherlands (brine purification wastes). In the US, industry and the regulatory community are pursuing the use of salt caverns for disposal of oil-field wastes. In 1988, the US Environmental Protection Agency (EPA) issued a regulatory determination exempting wastes generated during oil and gas exploration and production (oil-field wastes) from federal hazardous waste regulations--even though such wastes may contain hazardous constituents. At the same time, EPA urged states to tighten their oil-field waste management regulations. The resulting restrictions have generated industry interest in the use of salt caverns for potentially economical and environmentally safe oil-field waste disposal. Before the practice can be implemented commercially, however, regulators need assurance that disposing of oil-field wastes in salt caverns is technically and legally feasible and that potential health effects associated with the practice are acceptable. In 1996, Argonne National Laboratory (ANL) conducted a preliminary technical and legal evaluation of disposing of nonhazardous oil-field wastes (NOW) into salt caverns. It investigated regulatory issues; the types of oil-field wastes suitable for cavern disposal; cavern design and location considerations; and disposal operations, closure and remediation issues. It determined

High-temperature incineration of radioactive waste. Exploitation of the FLK-60 slagging incinerator for the treatment of different waste streams contaminated with plutonium

International Nuclear Information System (INIS)

Voorde Van de, N.; Taeymans, A.; Hennart, D.; Vanbrabant, R.; Balleux, W.; Geenen, G.; Gijbels, J.

1986-01-01

During the years 1983 and 1984 the FLK-60 high-temperature slagging incinerator at Mol was used for incineration of simulated plutonium waste and BWR power-station waste after extensive technical adaptations. A total of 10 tons of simulated waste containing 15 g of plutonium and 6 tons of simulated waste containing 624 MBq of 60 Co and 393 MBq of cesium isotopes was successfully treated. The average volume reduction factor was 18. Global decontamination factors of 280 000 for 137 Cs and 22 000 000 for 239 Pu were measured. Routine working and interventions for maintenance and repair could be carried out safely in alpha-conditions. The report describes in detail the technical adaptations and the behaviour of the various parts of the installation during the 39 runs carried out in the contract period. It also gives the chemical and radiochemical composition of the granules and secondary waste streams. The plutonium-based leach rate of the granules is in the range of 2 x 10 -5 to 3.5 x 10 -4 g/cm 2 . d. Finally typical mass, energy and radioactivity balances of the installation are given and various options for the final conditioning of the granules are briefly discussed. 6 refs, 6 figs, 29 tables

Pilot-Scale Removal Of Fluoride From Legacy Plutonium Materials Using Vacuum Salt Distillation

International Nuclear Information System (INIS)

Pierce, R. A.; Pak, D. J.

2012-01-01

Between September 2009 and January 2011, the Savannah River National Laboratory (SRNL) and HB-Line designed, developed, tested, and successfully deployed a system for the distillation of chloride salts. In 2011, SRNL adapted the technology for the removal of fluoride from fluoride-bearing salts. The method involved an in situ reaction between potassium hydroxide (KOH) and the fluoride salt to yield potassium fluoride (KF) and the corresponding oxide. The KF and excess KOH can be distilled below 1000°C using vacuum salt distillation (VSD). The apparatus for vacuum distillation contains a zone heated by a furnace and a zone actively cooled using either recirculated water or compressed air. During a vacuum distillation operation, a sample boat containing the feed material is placed into the apparatus while it is cool, and the system is sealed. The system is evacuated using a vacuum pump. Once a sufficient vacuum is attaned, heating begins. Volatile salts distill from the heated zone to the cooled zone where they condense, leaving behind the non-volatile material in the feed boat. Studies discussed in this report were performed involving the use of non-radioactive simulants in small-scale and pilot-scale systems as well as radioactive testing of a small-scale system with plutonium-bearing materials. Aspects of interest include removable liner design considerations, boat materials, in-line moisture absorption, and salt deposition

The treatment and packaging of waste plutonium and waste actinides for disposal

International Nuclear Information System (INIS)

Taylor, R.F.

1988-07-01

The objectives of this work have been to review the current state of knowledge on the treatment and packaging of unusable or surplus plutonium and other waste actinides for disposal and to identify any gaps in data essential for the development of a preferred route. The exercise was based on published data which said the quantity currently to be disposed of was 50 tonnes in oxide form. A literature review over the period 1978 to 1988 was carried out and a computerised database specific to the exercise was created. From this it is concluded that there are no insuperable problems to the formulation of a disposal route although there is none currently proven. The preferred wasteform would be a glass or synthetic rock. The major complication lies in the fissile nature of plutonium which dictates limits to the package size and places restrictions on the production and disposal routes. Additional work necessary to permit a final decision is listed. (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)

Is it possible to recycle nuclear wastes? Costs, risks and stakes of the plutonium industry; Peut-on recycler les dechets nucleaires? Couts, risques et enjeux de l'industrie du plutonium

Energy Technology Data Exchange (ETDEWEB)

NONE

2009-07-01

This document, published by the French association 'Sortir du nucleaire' (Get out of nuclear), gives some information on the chain reaction from uranium to plutonium, the difference between reprocessing (which does not reduce waste volumes but multiply waste types) and recycling, the high risks associated with plutonium transport, La Hague as the most dangerous nuclear site in France, reprocessing as the alibi for the French nuclear industry, Areva as an expert in propaganda, reprocessing as an absurd world strategy, plutonium as a fuel for proliferation, the myth of unlimited energy with the breeder reactors, and so on

Saltstone: cement-based waste form for disposal of Savannah River Plant low-level radioactive salt waste

International Nuclear Information System (INIS)

Langton, C.A.

1984-01-01

Defense waste processing at the Savannah River Plant will include decontamination and disposal of approximately 400 million liters of waste containing NaNO 3 , NaOH, Na 2 SO 4 , and NaNO 2 . After decontamination, the salt solution is classified as low-level waste. A cement-based waste form, saltstone, has been designed for disposal of Savannah River Plant low-level radioactive salt waste. Bulk properties of this material have been tailored with respect to salt leach rate, permeability, and compressive strength. Microstructure and mineralogy of leached and unleached specimens were characterized by SEM and x-ray diffraction analyses. The disposal system for the DWPF salt waste includes reconstitution of the crystallized salt as a solution containing 32 wt % solids. This solution will be decontaminated to remove 137 Cs and 90 Sr and then stabilized in a cement-based waste form. Laboratory and field tests indicate that this stabilization process greatly reduces the mobility of all of the waste constitutents in the surface and near-surface environment. Engineered trenches for subsurface burial of the saltstone have been designed to ensure compatibility between the waste form and the environment. The total disposal sytem, saltstone-trench-surrounding soil, has been designed to contain radionuclides, Cr, and Hg by both physical encapsulation and chemical fixation mechanisms. Physical encapsulation of the salts is the mechanism employed for controlling N and OH releases. In this way, final disposal of the SRP low-level waste can be achieved and the quality of the groundwater at the perimeter of the disposal site meets EPA drinking water standards

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

International Nuclear Information System (INIS)

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

2004-01-01

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

Potential role of ABC-assisted repositories in U.S. plutonium and high-level waste disposition

Energy Technology Data Exchange (ETDEWEB)

Berwald, D.; Favale, A.; Myers, T. [Grumman Aerospace Corporation, Bethpage, NY (United States)] [and others

1995-10-01

This paper characterizes the issues involving deep geologic disposal of LWR spent fuel rods, then presents results of an investigation to quantify the potential role of Accelerator-Based Conversion (ABC) in an integrated national nuclear materials and high level waste disposition strategy. The investigation used the deep geological repository envisioned for Yucca Mt., Nevada as a baseline and considered complementary roles for integrated ABC transmutation systems. The results indicate that although a U.S. geologic waste repository will continue to be required, waste partitioning and accelerator transmutation of plutonium, the minor actinides, and selected long-lived fission products can result in the following substantial benefits: plutonium burndown to near zero levels, a dramatic reduction of the long term hazard associated with geologic repositories, an ability to place several-fold more high level nuclear waste in a single repository, electricity sales to compensate for capital and operating costs.

Cerium, uranium, and plutonium behavior in glass-bonded sodalite, a ceramic nuclear waste form

International Nuclear Information System (INIS)

Lewis, M. A.; Lexa, D.; Morss, L. R.; Richmann, M. K.

1999-01-01

Glass-bonded sodalite is being developed as a ceramic waste form (CWF) to immobilize radioactive fission products, actinides, and salt residues from electrometallurgical treatment of spent nuclear reactor fuel. The CWF consists of about 75 mass % sodalite, 25 mass % glass, and small amounts of other phases. This paper presents some results and interpretation of physical measurements to characterize the CWF structure, and dissolution tests to measure the release of matrix components and radionuclides from the waste form. Tests have been carried out with specimens of the CWF that contain rare earths at concentrations similar to those expected in the waste form. Parallel tests have been carried out on specimens that have uranium or plutonium as well as the rare earths at concentrations similar to those expected in the waste forms; in these specimens UCl 3 forms UO 2 and PuCl 3 forms PuO 2 . The normalized releases of rare earths in dissolution tests were found to be much lower than those of matrix elements (B, Si, Al, Na). When there is no uranium in the CWF, the release of cerium is two to ten times lower than the release of the other rare earths. The low release of cerium may be due to its tetravalent state in uranium-free CWF. However, when there is uranium in the CWF, the release of cerium is similar to that of the other rare earths. This trivalent behavior of cerium is attributed to charge transfer or covalent interactions among cerium, uranium, and oxygen in (U,Ce)O 2

Stabilization Using Phosphate Bonded Ceramics. Salt Containing Mixed Waste Treatment. Mixed Waste Focus Area. OST Reference No. 117

International Nuclear Information System (INIS)

1999-01-01

Throughout the Department of Energy (DOE) complex there are large inventories of homogeneous mixed waste solids, such as wastewater treatment residues, fly ashes, and sludges that contain relatively high concentrations (greater than 15% by weight) of salts. The inherent solubility of salts (e.g., nitrates, chlorides, and sulfates) makes traditional treatment of these waste streams difficult, expensive, and challenging. One alternative is low-temperature stabilization by chemically bonded phosphate ceramics (CBPCs). The process involves reacting magnesium oxide with monopotassium phosphate with the salt waste to produce a dense monolith. The ceramic makes a strong environmental barrier, and the metals are converted to insoluble, low-leaching phosphate salts. The process has been tested on a variety of surrogates and actual mixed waste streams, including soils, wastewater, flyashes, and crushed debris. It has also been demonstrated at scales ranging from 5 to 55 gallons. In some applications, the CBPC technology provides higher waste loadings and a more durable salt waste form than the baseline method of cementitious grouting. Waste form test specimens were subjected to a variety of performance tests. Results of waste form performance testing concluded that CBPC forms made with salt wastes meet or exceed both RCRA and recommended Nuclear Regulatory Commission (NRC) low-level waste (LLW) disposal criteria. Application of a polymer coating to the CBPC may decrease the leaching of salt anions, but continued waste form evaluations are needed to fully assess the deteriorating effects of this leaching, if any, over time.

Treatment of waste salt from the advanced spent fuel conditioning process (I): characterization of Zeolite A in Molten LiCl Salt

International Nuclear Information System (INIS)

Kim, Jeong Guk; Lee, Jae Hee; Yoo, Jae Hyung; Kim, Joon Hyung

2004-01-01

The oxide fuel reduction process based on the electrochemical method (Advanced spent fuel Conditioning Process; ACP) and the long-lived radioactive nuclides partitioning process based on electro-refining process, which are being developed ay the Korea Atomic Energy Research Institute (KAERI), are to generate two types of molten salt wastes such as LiCl salt and LiCl-KCl eutectic salt, respectively. These waste salts must meet some criteria for disposal. A conditioning process for LiCl salt waste from ACP has been developed using zeolite A. This treatment process of waste salt using zeolite A was first developed by US ANL (Argonne National Laboratory) for LiCl-KCl eutectic salt waste from an electro-refining process of EBR (Experimental Breeder Reactor)-II spent fuel. This process has been developed recently, and a ceramic waste form (CWF) is produced in demonstration-scale V-mixer (50 kg/batch). However, ANL process is different from KAERI treatment process in waste salt, the former is LiCl-KCl eutectic salt and the latter is LiCl salt. Because of melting point, the immobilization of eutectic salt is carried out at about 770 K, whereas LiCl salt at around 920 K. Such difference has an effect on properties of immobilization media, zeolite A. Here, zeolite A in high-temperature (923 K) molten LiCl salt was characterized by XRD, Ion-exchange, etc., and evaluated if a promising media or not

Expected brine movement at potential nuclear waste repository salt sites

International Nuclear Information System (INIS)

McCauley, V.S.; Raines, G.E.

1987-08-01

The BRINEMIG brine migration code predicts rates and quantities of brine migration to a waste package emplaced in a high-level nuclear waste repository in salt. The BRINEMIG code is an explicit time-marching finite-difference code that solves a mass balance equation and uses the Jenks equation to predict velocities of brine migration. Predictions were made for the seven potentially acceptable salt sites under consideration as locations for the first US high-level nuclear waste repository. Predicted total quantities of accumulated brine were on the order of 1 m 3 brine per waste package or less. Less brine accumulation is expected at domal salt sites because of the lower initial moisture contents relative to bedded salt sites. Less total accumulation of brine is predicted for spent fuel than for commercial high-level waste because of the lower temperatures generated by spent fuel. 11 refs., 36 figs., 29 tabs

Recent studies of uranium and plutonium chemistry in alkaline radioactive waste solutions

International Nuclear Information System (INIS)

King, William D.; Wilmarth, William R.; Hobbs, David T.; Edwards, Thomas B.

2008-01-01

Solubility studies of uranium and plutonium in a caustic, radioactive Savannah River Site tank waste solution revealed the existence of uranium supersaturation in the as-received sample. Comparison of the results to predictions generated from previously published models for solubility in these waste types revealed that the U model poorly predicts solubility while Pu model predictions are quite consistent with experimental observations. Separate studies using simulated Savannah River Site evaporator feed solution revealed that the known formation of sodium aluminosilicate solids in waste evaporators can promote rapid precipitation of uranium from supersaturated solutions

Release rates from waste packages in a salt repository

International Nuclear Information System (INIS)

Chambre, P.L.; Hwang, Y.; Lee, W.W.L.; Pigford, T.H.

1987-06-01

In this report we present estimates of radionuclide release rates from waste packages into salt. This conservative and bounding analysis shows that release rates from waste packages in salt are well below the US Nuclear Regulatory Commission's performance objectives for the engineered barrier system. 2 refs., 2 figs

Molecular dynamics study of a nuclear waste glass matrix with plutonium

International Nuclear Information System (INIS)

Meis, C.; Delaye, J.M.; Ghaleb, D.

1999-01-01

Molecular dynamics simulation techniques were applied to model the incorporation of plutonium in the French nuclear waste glass matrix. Born-Mayer-Huggins analytical potentials were established to characterize short-range interactions between Pu-O and Pu-Pu pairs; the potentials were fitted to the structural properties of plutonium dioxide in the light of a recent experimental study showing that plutonium is found as Pu(IV) in the glass. The transferability of the established potentials to the glass structure is discussed, and the potential parameters are further refined by molecular dynamics simulations in an aluminoborosilicate glass to obtain mean Pu-O interatomic distances and first-neighbor coordination numbers matching the experimental values as closely as possible. Previously published Born-Mayer-Huggins potentials supplemented by Stillinger-Weber three-body terms were used for oxygen-cation and cation-cation interactions. The difficulties encountered in establishing a Pu-O potential that provides satisfactory results in both oxides and glasses are also discussed

Estimate of the Sources of Plutonium-Containing Wastes Generated from MOX Fuel Production in Russia

International Nuclear Information System (INIS)

Kudinov, K.G.; Tretyakov, A.A.; Sorokin, Y.P.; Bondin, V.V.; Manakova, L.F.; Jardine, L.J.

2001-01-01

In Russia, mixed oxide (MOX) fuel is produced in a pilot facility ''Paket'' at ''MAYAK'' Production Association. The Mining-Chemical Combine (MCC) has developed plans to design and build a dedicated industrial-scale plant to produce MOX fuel and fuel assemblies (FA) for VVER-1000 water reactors and the BN-600 fast-breeder reactor, which is pending an official Russian Federation (RF) site-selection decision. The design output of the plant is based on production capacity of 2.75 tons of weapons plutonium per year to produce the resulting fuel assemblies: 1.25 tons for the BN-600 reactor FAs and the remaining 1.5 tons for VVER-1000 FAs. It is likely the quantity of BN-600 FAs will be reduced in actual practice. The process of nuclear disarmament frees a significant amount of weapons plutonium for other uses, which, if unutilized, represents a constant general threat. In France, Great Britain, Belgium, Russia, and Japan, reactor-grade plutonium is used in MOX-fuel production. Making MOX-fuel for CANDU (Canada) and pressurized water reactors (PWR) (Europe) is under consideration Russia. If this latter production is added, as many as 5 tons of Pu per year might be processed into new FAs in Russia. Many years of work and experience are represented in the estimates of MOX fuel production wastes derived in this report. Prior engineering studies and sludge treatment investigations and comparisons have determined how best to treat Pu sludges and MOX fuel wastes. Based upon analyses of the production processes established by these efforts, we can estimate that there will be approximately 1200 kg of residual wastes subject to immobilization per MT of plutonium processed, of which approximately 6 to 7 kg is Pu in the residuals per MT of Pu processed. The wastes are various and complicated in composition. Because organic wastes constitute both the major portion of total waste and of the Pu to be immobilized, the recommended treatment of MOX-fuel production waste is incineration

Laboratory simulation of salt dissolution during waste removal

International Nuclear Information System (INIS)

Wiersma, B.J.; Parish, W.R.

1997-01-01

Laboratory experiments were performed to support the field demonstration of improved techniques for salt dissolution in waste tanks at the Savannah River Site. The tests were designed to investigate three density driven techniques for salt dissolution: (1) Drain-Add-Sit-Remove, (2) Modified Density Gradient, and (3) Continuous Salt Mining. Salt dissolution was observed to be a very rapid process as salt solutions with densities between 1.38-1.4 were frequently removed. Slower addition and removal rates and locating the outlet line at deeper levels below the top of the saltcake provided the best contact between the dissolution water and the saltcake. It was observed that dissolution with 1 M sodium hydroxide solution resulted in salt solutions that were within the current inhibitor requirements for the prevention of stress corrosion cracking. This result was independent of the density driven technique. However, if inhibited water (0.01 M sodium hydroxide and 0.011 M sodium nitrite) was utilized, the salt solutions were frequently outside the inhibitor requirements. Corrosion testing at conditions similar to the environments expected during waste removal was recommended

The safe disposal of radioactive wastes in geologic salt formations

International Nuclear Information System (INIS)

Kuehn, K.; Proske, R.

Geologic salt formations appear to be particularly suitable for final storage. Their existance alone - the salt formations in Northern Germany are more than 200 million years old - is proof of their stability and of their isolation from biological cycles. In 1967 the storage of LAW and later, in 1972, of MAW was started in the experimental storage area Asse, south-east of Braunschweig, after the necessary technical preparations had been made. In more than ten years of operation approx. 114,000 drums of slightly active and 1,298 drums of medium-active wastes were deposited without incident. Methods have been developed for filling the available caverns with wastes and salt to ensure the security of long term disposal without supervision. Tests with electric heaters for simulation of heat-generating highly active wastes confirm the good suitability of salt formations for storing these wastes. Safety analyses for the operating time as well as for the long term phase after closure of the final storage area, which among others also comprise the improbable ''greatest expected accident'', namely break through of water, are carried out and confirm the safety of ultimate storage of radioactive wastes in geological salt formations. (orig./HP) [de

Accelerator-based systems for plutonium destruction and nuclear waste transmutation

International Nuclear Information System (INIS)

Arthur, E.D.

1994-01-01

Accelerator-base systems are described that can eliminate long-lived nuclear materials. The impact of these systems on global issues relating to plutonium minimization and nuclear waste disposal can be significant. An overview of the components that comprise these systems is given, along with discussion of technology development status and needs. A technology development plan is presented with emphasis on first steps that would demonstrate technical performance

Decontamination of alpha-bearing solid wastes and plutonium recovery

International Nuclear Information System (INIS)

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

1993-01-01

Nuclear activities in the Radiochemistry building of Fontenay-aux-Roses Nuclear Research Center concern principally the study of fuel reprocessing and the production of transuranium isotopes. During these activities solid wastes are produced. In order to improve the management of these wastes, it has been decided to build new facilities: a group of three glove-boxes named ELISE for the treatment of α active solid waste and a hot-cell, PROLIXE, for the treatment of solid wastes. Leaching processes were developed in order to: decontaminate these wastes and recover actinide elements, particularly the highly valuable plutonium, from the leachates. The processes developed are sufficiently flexible to be able to accommodate solid wastes produced in other facilities. Laboratory studies were conducted to develop the leaching process based on the use of electrogenerated Ag(II) species which is particularly suitable to provoke the dissolution of PuO 2 . Successful exhaustive Pu decontaminations with DF(Pu) higher than 10 4 were achieved for the first time during the treatment of stainless steel PuO 2 cans (future MELOX plant) by electrogenerated Ag (II) in nitric acid medium

Spent fuel, plutonium and nuclear waste: long-term management; Le combustible use et le plutonium en tant que dechets nucleaires: gestion a long terme

Energy Technology Data Exchange (ETDEWEB)

Collard, G

1998-11-01

Different options for the management of nuclear waste arising from the nuclear fuel cycle are discussed. Special emphasis is on reprocessing followed by geological disposal, geological disposal of reprocessing waste, direct geological disposal of spent nuclear fuel, long term storage. Particular emphasis is on the management of plutonium including recycling, immobilisation and disposal, partitioning and transmutation.

Alternative methods of salt disposal at the seven salt sites for a nuclear waste repository

International Nuclear Information System (INIS)

1987-02-01

This study discusses the various alternative salt management techniques for the disposal of excess mined salt at seven potentially acceptable nuclear waste repository sites: Deaf Smith and Swisher Counties, Texas; Richton and Cypress Creek Domes, Mississippi; Vacherie Dome, Louisiana; and Davis and Lavender Canyons, Utah. Because the repository development involves the underground excavation of corridors and waste emplacement rooms, in either bedded or domed salt formations, excess salt will be mined and must be disposed of offsite. The salt disposal alternatives examined for all the sites include commercial use, ocean disposal, deep well injection, landfill disposal, and underground mine disposal. These alternatives (and other site-specific disposal methods) are reviewed, using estimated amounts of excavated, backfilled, and excess salt. Methods of transporting the excess salt are discussed, along with possible impacts of each disposal method and potential regulatory requirements. A preferred method of disposal is recommended for each potentially acceptable repository site. 14 refs., 5 tabs

On the Burning of Plutonium Originating from Light Water Reactor Use in a Fast Molten Salt Reactor—A Neutron Physical Study

Directory of Open Access Journals (Sweden)

Bruno Merk

2015-11-01

Full Text Available An efficient burning of the plutonium produced during light water reactor (LWR operation has the potential to significantly improve the sustainability indices of LWR operations. The work offers a comparison of the efficiency of Pu burning in different reactor configurations—a molten salt fast reactor, a LWR with mixed oxide (MOX fuel, and a sodium cooled fast reactor. The calculations are performed using the HELIOS 2 code. All results are evaluated against the plutonium burning efficiency determined in the Consommation Accrue de Plutonium dans les Réacteurs à Neutrons RApides (CAPRA project. The results are discussed with special view on the increased sustainability of LWR use in the case of successful avoidance of an accumulation of Pu which otherwise would have to be forwarded to a final disposal. A strategic discussion is given about the unavoidable plutonium production, the possibility to burn the plutonium to avoid a burden for the future generations which would have to be controlled.

Removal of actinides from selected nuclear fuel reprocessing wastes

International Nuclear Information System (INIS)

Navratil, J.D.; Thompson, G.H.

1979-01-01

The US Department of Energy awarded Oak Ridge National Laboratory a program to develop a cost-risk-benefit analysis of partitioning long-lived nuclides from waste and transmuting them to shorter lived or stable nuclides. Two subtasks of this program were investigated at Rocky Flats. In the first subtask, methods for solubilizing actinides in incinerator ash were tested. Two methods appear to be preferable: reaction with ceric ion in nitric acid or carbonate-nitrate fusion. The ceric-nitric acid system solubilizes 95% of the actinides in ash; this can be increased by 2 to 4% by pretreating ash with sodium hydroxide to solubilize silica. The carbonate-nitrate fusion method solubilizes greater than or equal to 98% of the actinides, but requires sodium hydroxide pretreatment. Two additional disadvantages are that it is a high-temperature process, and that it generates a lot of salt waste. The second subtask comprises removing actinides from salt wastes likely to be produced during reactor fuel fabrication and reprocessing. A preliminary feasibility study of solvent extraction methods has been completed. The use of a two-step solvent extraction system - tributyl phosphate (TBP) followed by extraction with a bidentate organophosphorous extractant (DHDECMP) - appears to be the most efficient for removing actinides from salt waste. The TBP step would remove most of the plutonium and > 99.99% of the uranium. The second step using DHDECMP would remove > 99.91% of the americium and the remaining plutonium (> 99.98%) and other actinides from the acidified salt waste. 8 figures, 11 tables

Defense waste salt disposal at the Savannah River Plant

International Nuclear Information System (INIS)

Langton, C.A.; Dukes, M.D.

1984-01-01

A cement-based waste form, saltstone, has been designed for disposal of Savannah River Plant low-level radioactive salt waste. The disposal process includes emplacing the saltstone in engineered trenches above the water table but below grade at SRP. Design of the waste form and disposal system limits the concentration of salts and radionuclides in the groundwater so that EPA drinking water standards will not be exceeded at the perimeter of the disposal site. 10 references, 4 figures, 3 tables

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

Expedited demonstration of molten salt mixed waste treatment technology. Final report

International Nuclear Information System (INIS)

1995-01-01

This final report discusses the molten salt mixed waste project in terms of the various subtasks established. Subtask 1: Carbon monoxide emissions; Establish a salt recycle schedule and/or a strategy for off-gas control for MWMF that keeps carbon monoxide emission below 100 ppm on an hourly averaged basis. Subtask 2: Salt melt viscosity; Experiments are conducted to determine salt viscosity as a function of ash composition, ash concentration, temperature, and time. Subtask 3: Determine that the amount of sodium carbonate entrained in the off-gas is minimal, and that any deposited salt can easily be removed form the piping using a soot blower or other means. Subtask 4: The provision of at least one final waste form that meets the waste acceptance criteria of a landfill that will take the waste. This report discusses the progress made in each of these areas

Salt Repository Project Waste Package Program Plan: Draft

International Nuclear Information System (INIS)

Carr, J.A.; Cunnane, J.C.

1986-01-01

Under the direction of the Office of Civilian Radioactive Waste Management (OCRWM) created within the DOE by direction of the Nuclear Waste Policy Act of 1982 (NWPA), the mission of the Salt Repository Project (SRP) is to provide for the development of a candidate salt repository for disposal of high-level radioactive waste (HLW) and spent reactor fuel in a manner that fully protects the health and safety of the public and the quality of the environment. In consideration of the program needs and requirements discussed above, the SRP has decided to develop and issue this SRP Waste Package Program Plan. This document is intended to outline how the SRP plans to develop the waste package design and to show, with reasonable assurance, that the developed design will satisfy applicable requirements/performance objectives. 44 refs., 16 figs., 16 tabs

Radioactive waste management and disposal

International Nuclear Information System (INIS)

Simon, R.; Orlowski, S.

1980-01-01

The first European Community conference on Radioactive Waste Management and Disposal was held in Luxembourg, where twenty-five papers were presented by scientists involved in European Community contract studies and by members of the Commission's scientific staff. The following topics were covered: treatment and conditioning technology of solid intermediate level wastes, alpha-contaminated combustible wastes, gaseous wastes, hulls and dissolver residues and plutonium recovery; waste product evaluation which involves testing of solidified high level wastes and other waste products; engineering storage of vitrified high level wastes and gas storage; and geological disposal in salt, granite and clay formations which includes site characterization, conceptual repository design, waste/formation interactions, migration of radionuclides, safety analysis, mathematical modelling and risk assessment

Salt splitting of sodium-dominated radioactive waste using ceramic membranes

International Nuclear Information System (INIS)

Hollenberg, G.W.; Carlson, C.D.; Virkar, A.; Joshi, A.

1994-08-01

The potential for salt splitting of sodium dominated radioactive wastes by use of a ceramic membrane is reviewed. The technical basis for considering this processing technology is derived from the technology developed for battery and chlor-alkali chemical industry. Specific comparisons are made with the commercial organic membranes which are the standard in nonradioactive salt splitting. Two features of ceramic membranes are expected to be especially attractive: high tolerance to gamma irradiation and high selectivity between sodium and other ions. The objective of the salt splitting process is to separate nonradioactive sodium from contaminated sodium salts prior to other pretreatment processes in order to: (1) concentrate the waste in order to reduce the volume of subsequent additives and capacity of equipment, (2) decrease the pH of the waste in preparation for further processing, and (3) provide sodium with very low radioactivity levels for caustic washing of sludge or low level and mixed waste vitrification

Review of major plutonium pyrochemical technology

International Nuclear Information System (INIS)

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

1983-01-01

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

Molten salt destruction process for mixed wastes

International Nuclear Information System (INIS)

Upadhye, R.S.; Wilder, J.G.; Karlsen, C.E.

1993-04-01

We are developing an advanced two-stage process for the treatment of mixed wastes, which contain both hazardous and radioactive components. The wastes, together with an oxidant gas, such as air, are injected into a bed of molten salt comprising a mixture of sodium-, potassium-, and lithium-carbonates, with a melting point of about 580 degree C. The organic constituents of the mixed waste are destroyed through the combined effect of pyrolysis and oxidation. Heteroatoms. such as chlorine, in the mixed waste form stable salts, such as sodium chloride, and are retained in the melt. The radioactive actinides in the mixed waste are also retained in the melt because of the combined action of wetting and partial dissolution. The original process, consists of a one-stage unit, operated at 900--1000 degree C. The advanced two-stage process has two stages, one for pyrolysis and one for oxidation. The pyrolysis stage is designed to operate at 700 degree C. The oxidation stage can be operated at a higher temperature, if necessary

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

Generic waste management concepts for six LWR fuel cycles

International Nuclear Information System (INIS)

DePue, J.D.

1979-04-01

This report supplements the treatment of waste management issues provided in the Generic Environmental Statement on the use of recycle plutonium in mixed oxide fuel in light water cooled reactors (GESMO, NUREG-0002). Three recycle and three no-recycle options are described in this document. Management of the radioactive wastes that would result from implementation of either type of fuel cycle alternative is discussed. For five of the six options, wastes would be placed in deep geologic salt repositories for which thermal criteria are considered. Radiation doses to the workers at the repositories and to the general population are discussed. The report also covers the waste management schedule, the land and salt commitments, and the economic costs for the management of wastes generated

R and D activities on the management of waste chloride salts in KAERI

International Nuclear Information System (INIS)

In-Tae, Kim; Hwan-Seo, Park; Jeong-Gook, Kim; Hee-Chul, Yang; Yong-Joon, Cho; Eung-Ho Kim

2007-01-01

Full text of publication follows. Electrochemical treatment of spent oxide fuels has been intensively studied in KAERI to reduce the volume, heat load and radiotoxicity of high-level wastes. It consists of an electrolytic reduction process to convert the oxide fuel into a metallic form and an electro-refining process to separate TRU elements from the electro-reduced metal ingot. Two types of waste salts are expected to generate from the electrochemical pyro-processes, that is, LiCl salt from the reduction process and LiCl+KCl eutectic salt form the refining process. The R and D strategy of the waste salt management in KAERI can be categorized into two parts: 1) enhancement of safety by the stabilisation/solidification of waste salt that is to be finally disposed of and 2) reduction of the waste generation by the regeneration/recycle of the spent salt after removal of radionuclides in it. A sol-gel technique and a zeolite occlusion technique are under development to stabilize the waste salt. The LiCl salt is stabilised by a low-temperature sol-gel process and then the gel product is solidified into a ceramic-like waste form with an addition of glass frit. Another method uses Zeolite-4A to occlude the LiCl salt into its cage and adsorption site to immobilize the radionuclides. The product, salt-occluded zeolite, is fabricated into another type of a ceramic waste form. For the regeneration and recycle of the spent salt, the radionuclides in the salt are removed by a zeolite process for the LiCl salt and by an oxidation/distillation process for the eutectic salt. The target nuclides to be removed in each process are Cs/Sr and rare earth (RE) elements, respectively. In the oxidation/ distillation process, the rare earth chloride nuclides are oxidised by an oxygen sparging method, and the products are precipitated in the form of oxide or oxychloride REs. After separation of the RE elements from the precipitates by distillation, the refined spent salt with a low content

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

Energy Technology Data Exchange (ETDEWEB)

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

1967-03-01

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

Containment of solidified liquid hazardous waste in domal salt

International Nuclear Information System (INIS)

Domenico, P.A.; Lerman, A.

1992-01-01

In recent years, the solidification of hazardous liquid waste has become a viable option in waste management. The solidification process results in an increased volume but more stable waste form that must be disposed of or stored in a dry environment. An environment of choice in south central Texas is domal salt. The salt dome currently under investigation has a water content of 0.002 percent by weight and a permeability less than one nanodarcy. A question that must be addressed is whether a salt dome has a particular set of attributes that will prevent the release of contaminants to the environment. From a regulatory perspective, a ''no migration'' petition must be approved by the U.S.E.P.A. for the containment facility. By ''no migration'' it is implied that the waste must be contained for 10,000 years. A demonstration that this condition will be met will require model calculations and such models must be based on the physical and chemical characteristics of the waste form and the geologic environment. In particular, the models must address the rate of brine infiltration into the caverns, providing information on how fast an immobile solid waste form could convert to a more mobile liquid state. Additionally, the potential for migration by both diffusion and advection is of concern. Lastly, given a partially saturated cavern, the question of how far gaseous waste will be transported over the 10,000 year containment period must also be addressed. Results indicate that the containment capabilities of domal salt are exceptional. A nominal volume of brine will seep into the cavern and most voids between the injected solidified waste pellets will remain unsaturated. Very small quantities of hazardous constituents will be leached from the waste pellets

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

International Nuclear Information System (INIS)

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

1978-11-01

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

Characterisation of Plasma Vitrified Simulant Plutonium Contaminated Material Waste

International Nuclear Information System (INIS)

Hyatt, Neil C.; Morgan, Suzy; Stennett, Martin C.; Scales, Charlie R.; Deegan, David

2007-01-01

The potential of plasma vitrification for the treatment of a simulant Plutonium Contaminated Material (PCM) was investigated. It was demonstrated that the PuO 2 simulant, CeO 2 , could be vitrified in the amorphous calcium iron aluminosilicate component of the product slag with simultaneous destruction of the organic and polymer waste fractions. Product Consistency Tests conducted at 90 deg. C in de-ionised water and buffered pH 11 solution show the PCM slag product to be durable with respect to release of Ce. (authors)

Design-Only Conceptual Design Report: Plutonium Immobilization Plant

International Nuclear Information System (INIS)

DiSabatino, A.; Loftus, D.

1999-01-01

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

Characteristics of solidified products containing radioactive molten salt waste.

Science.gov (United States)

Park, Hwan-Seo; Kim, In-Tae; Cho, Yong-Zun; Eun, Hee-Chul; Kim, Joon-Hyung

2007-11-01

The molten salt waste from a pyroprocess to recover uranium and transuranic elements is one of the problematic radioactive wastes to be solidified into a durable wasteform for its final disposal. By using a novel method, named as the GRSS (gel-route stabilization/solidification) method, a molten salt waste was treated to produce a unique wasteform. A borosilicate glass as a chemical binder dissolves the silicate compounds in the gel products to produce one amorphous phase while most of the phosphates are encapsulated by the vitrified phase. Also, Cs in the gel product is preferentially situated in the silicate phase, and it is vitrified into a glassy phase after a heat treatment. The Sr-containing phase is mainly phosphate compounds and encapsulated by the glassy phase. These phenomena could be identified by the static and dynamic leaching test that revealed a high leach resistance of radionuclides. The leach rates were about 10(-3) - 10(-2) g/m2 x day for Cs and 10(-4) - 10(-3) g/m2 x day for Sr, and the leached fractions of them were predicted to be 0.89% and 0.39% at 900 days, respectively. This paper describes the characteristics of a unique wasteform containing a molten salt waste and provides important information on a newly developed immobilization technology for salt wastes, the GRSS method.

Problems of the final storage of radioactive waste in salt formations

International Nuclear Information System (INIS)

Hofrichter, E.

1977-01-01

The geological conditions for the final storage of radioactive waste, the occurrence of salt formations, and the tectonics of salt domes are discussed. The safety of salt rocks, the impermeability of the rocks, and the thermal problems in the storage of high-activity waste are dealt with. Possibilities and preconditions of final storage in West Germany are discussed. (HPH) [de

Thermal denitration of high concentration nitrate salts waste water

International Nuclear Information System (INIS)

Hwang, D. S.; Oh, J. H.; Choi, Y. D.; Hwang, S. T.; Park, J. H.; Latge, C.

2003-01-01

This study investigated the thermodynamic and the thermal decomposition properties of high concentration nitrate salts waste water for the lagoon sludge treatment. The thermodynamic property was carried out by COACH and GEMINI II based on the composition of nitrate salts waste water. The thermal decomposition property was carried out by TG-DTA and XRD. Ammonium nitrate and sodium nitrate were decomposed at 250 .deg. C and 730 . deg. C, respectively. Sodium nitrate could be decomposed at 450 .deg. C in the case of adding alumina for converting unstable Na 2 O into stable Na 2 O.Al 2 O 3 . The flow sheet for nitrate salts waste water treatment was proposed based on the these properties data. These will be used by the basic data of the process simulation

Method to synthesize dense crystallized sodalite pellet for immobilizing halide salt radioactive waste

International Nuclear Information System (INIS)

Koyama, Tadafumi.

1994-01-01

A method is described for immobilizing waste chloride salts containing radionuclides such as cesium and strontium and hazardous materials such as barium. A sodalite intermediate is prepared by mixing appropriate amounts of silica, alumina and sodium hydroxide with respect to sodalite and heating the mixture to form the sodalite intermediate and water. Heating is continued to drive off the water to form a water-free intermediate. The water-free intermediate is mixed with either waste salt or waste salt which has been contacted with zeolite to concentrate the radionuclides and hazardous material. The waste salt-intermediate mixture is then compacted and heated under conditions of heat and pressure to form sodalite with the waste salt, radionuclides and hazardous material trapped within the sodalite cage structure. This provides a final product having excellent leach resistant capabilities

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.)

Plutonium contaminated materials research programme

International Nuclear Information System (INIS)

Higson, S.G.

1986-01-01

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

Use of plutonium and minor actinides as fuel in high temperature pebble bed reactors for waste minimization

International Nuclear Information System (INIS)

Meier, Astrid; Bernnat, Wolfgang; Lohnert, Guenther

2009-01-01

Energy production by nuclear fission gives rise to longlived radionuclides, such as plutonium and americium. The ''PuMA'' (Plutonium and Minor Actinides Waste Management) research project within the 6th Framework Program of the European Union serves to minimize waste arisings and transmute plutonium and minor actinides from spent LWR fuel elements by means of modular high-temperature reactors (HTR). Coating the fuel, which consists of kernels approx. 250 μm in radius and surrounded by graphite as the moderator material, allows very high operating and accident temperatures and very high burnups. One point examined is whether the inherent safety characteristics known for uranium oxide also exist for (PuO 2 + MAO 2 ) fuel. On the basis of a reference reactor similar to the South African PBMR-400, various loading strategies at maximum burnup are considered with a view to the inherent safety of the HTR. (orig.)

Management of radioactive waste and plutonium in the Swedish perspective

International Nuclear Information System (INIS)

Larsson, A.; Hultgren, A.; Lind, J.

1977-01-01

In May 1976 the Governmental Committee on Radioactive Waste (the Aka Committee) submitted its final report to the Swedish Government. The report summarizes a thorough investigation of questions dealing with spent nuclear fuel and radioactive waste. For Sweden, the study recommends reprocessing of spent fuel as a primary alternative. This should be closely linked with fabrication of mixed oxide fuel from recovered material for rapid return as fresh fuel in the energy producing reactors. Such a scheme would have the double advantage of both facilitating waste management and avoiding stockpiling of pure plutonium. The possibility to treat the spent fuel entirely as waste, not utilizing its fuel value, was also considered. Basically national reprocessing, including possibilities for international, particularly Nordic, regional collaboration is envisaged by the Committee. The findings and proposals of the Committee are discussed in the light of the recent development on the nuclear scene in Sweden. As to the economic side, it is argued that the utilities should include all costs relating to the back end in the budgets for their energy production programmes. Reprocessing and waste management neither can nor should be seen as ordinary commercial ventures. Consequently the planning to cover the important needs at the back end of the nuclear fuel cycle is hardly likely to be initiated and undertaken by means of the market mechanism. Careful efforts in this regard are instead required at the national and international levels. The particular sensitivity connected with spent nuclear fuel and plutonium is derived from concern relating to environmental safety and proliferation of nuclear weapons. Together with economic and technical considerations these two broad categories of concern, including physical security and safeguardability, are crucial in the selection and precise formulation of alternatives to be chosen for the back end of the nuclear fuel cycle. Also affecting

Incineration of simulated plutonium-contaminated waste

International Nuclear Information System (INIS)

Ford, L.H.; Jenkins, M.J.

1984-01-01

Pyrolysis rate data are presented which will enable larger pyrolyser furnaces to be made for processing solid plutonium-contaminated materials at throughputs of up to 20 kg/h using either 1 or 2.5 kg packages as feed. The influence of liquids, such as water, kerosene or oil, on the pyrolysis process has also been assessed. The products of pyrolysis for a range of individual materials and their mixtures have been defined. The oxidation rates for both static and stirred beds of char have been obtained. The implications of both the pyrolysis and char-oxidation processes for plant design are discussed. This work has been commissioned by the Department of the Environment as part of its radioactive waste management programme. The results will be used in the formulation of government policy, but as this stage they do not necessarily represent that policy

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

International Nuclear Information System (INIS)

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

2016-01-01

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

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

Energy Technology Data Exchange (ETDEWEB)

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

2016-06-13

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

Assessment of crushed salt consolidation and fracture healing processes in a nuclear waste repository in salt

International Nuclear Information System (INIS)

1984-11-01

For a nuclear waste repository in salt, two aspects of salt behavior are expected to contribute to favorable conditions for waste isolation. First, consolidation of crushed salt backfill due to creep closure of the underground openings may result in a backfill barrier with low permeability. Second, fractures created in the salt by excavation may heal under the influence of stress and temperature following sealing. This report reviews the status of knowledge regarding crushed salt consolidation and fracture healing, provides analyses which predict the rates at which the processes will occur under repository conditions, and develops requirements for future study. Analyses of the rate at which crushed salt will consolidate are found to be uncertain because of unexplained wide variation in the creep properties of crushed salt obtained from laboratory testing, and because of uncertainties in predictions of long term closure rates of openings in salt. This uncertainty could be resolved to a large degree by additional laboratory testing of crushed salt. Similarly, additional testing of fracture healing processes is required to confirm that healing will be effective under repository conditions. Extensive references, 27 figures, 5 tables

Systems costs for disposal of Savannah River high-level waste sludge and salt

International Nuclear Information System (INIS)

McDonell, W.R.; Goodlett, C.B.

1984-01-01

A systems cost model has been developed to support disposal of defense high-level waste sludge and salt generated at the Savannah River Plant. Waste processing activities covered by the model include decontamination of the salt by a precipitation process in the waste storage tanks, incorporation of the sludge and radionuclides removed from the salt into glass in the Defense Waste Processing Facility (DWPF), and, after interim storage, final disposal of the DWPF glass waste canisters in a federal geologic repository. Total costs for processing of waste generated to the year 2000 are estimated to be about $2.9 billion (1984 dollars); incremental unit costs for DWPF and repository disposal activities range from $120,000 to $170,000 per canister depending on DWPF processing schedules. In a representative evaluation of process alternatives, the model is used to demonstrate cost effectiveness of adjustments in the frit content of the waste glass to reduce impacts of wastes generated by the salt decontamination operations. 13 references, 8 tables

Research Program to Determine Redox Reactions and Their Effects on Speciation and Mobility of Plutonium in DOE Wastes

International Nuclear Information System (INIS)

Choppin, G.R.; Rai, D.

2000-01-01

Plutonium in geologic matrices undergoes a variety of complex reactions which complicate its environmental behavior. These complexities in plutonium chemistry whereby a large variety of precipitation, dissolution, adsorption/desorption, and redox reactions control plutonium speciation and concentrations, result in the need for a rather large amount of reliable, fundamental data to predict Pu behavior in geologic media. These data are also needed for evaluation of remediation strategies that involve removing most of the contaminants by selective methods, followed by in situ immobilization of residual contaminants. Two areas were studied during this project: (1) thermodynamic data for Th(IV) and Pu(IV) complexes of EDTA and for Pu(V) interactions with chloride; (2) kinetic data for redox reactions of Pu in the presence of common redox agents (e.g., H 2 O 2 , MnO 2 , and NaOCl) encountered under waste disposal conditions. These studies are relevant to understanding Pu behavior in wastes disposed of in diverse geologic conditions (e.g., at the WIPP and YUCCA Mountain repositories and in contaminated sediments at many different DOE sites) and also for developing effective remediation strategies (e.g., processing of high level waste tanks). These studies have yielded data to address redox reactions of plutonium in the presence of environmentally important agents (e.g. organic and inorganic oxidants/reductants)

Research Program to Determine Redox Reactions and Their Effects on Speciation and Mobility of Plutonium in DOE Wastes

Energy Technology Data Exchange (ETDEWEB)

Choppin, G.R.; Rai, D.

2000-10-01

Plutonium in geologic matrices undergoes a variety of complex reactions which complicate its environmental behavior. These complexities in plutonium chemistry whereby a large variety of precipitation, dissolution, adsorption/desorption, and redox reactions control plutonium speciation and concentrations, result in the need for a rather large amount of reliable, fundamental data to predict Pu behavior in geologic media. These data are also needed for evaluation of remediation strategies that involve removing most of the contaminants by selective methods, followed by in situ immobilization of residual contaminants. Two areas were studied during this project: (1) thermodynamic data for Th(IV) and Pu(IV) complexes of EDTA and for Pu(V) interactions with chloride; (2) kinetic data for redox reactions of Pu in the presence of common redox agents (e.g., H{sub 2}O{sub 2}, MnO{sub 2}, and NaOCl) encountered under waste disposal conditions. These studies are relevant to understanding Pu behavior in wastes disposed of in diverse geologic conditions (e.g., at the WIPP and YUCCA Mountain repositories and in contaminated sediments at many different DOE sites) and also for developing effective remediation strategies (e.g., processing of high level waste tanks). These studies have yielded data to address redox reactions of plutonium in the presence of environmentally important agents (e.g. organic and inorganic oxidants/reductants).

Plutonium Finishing Plant (PFP) Waste Composition and High Efficiency Particulate Air Filter Loading

Energy Technology Data Exchange (ETDEWEB)

ZIMMERMAN, B.D.

2000-12-11

This analysis evaluates the effect of the Plutonium Finishing Plant (PFP) waste isotopic composition on Tank Farms Final Safety Analysis Report (FSAR) accidents involving high-efficiency particulate air (HEPA) filter failure in Double-Contained Receiver Tanks (DCRTs). The HEPA Filter Failure--Exposure to High Temperature or Pressure, and Steam Intrusion From Interfacing Systems accidents are considered. The analysis concludes that dose consequences based on the PFP waste isotopic composition are bounded by previous FSAR analyses. This supports USQD TF-00-0768.

Investigation of Various LiCl Waste Salt Purification Technologies

International Nuclear Information System (INIS)

Yung-Zun Cho; Hee-Chul Yang; Han-Soo Lee; In-Tae Kim

2008-01-01

Various purification research of LiCl waste molten salt generated from electroreduction process were tested. The purification of the LiCl waste salt very important in a various aspects, where the purification means separation of cesium and strontium form LiCl salt melts. In this study, for the separation of cesium and strontium from LiCl salt melts, precipitant agent addition techniques such as sulfate and carbonate addition method and, as a new attempt, zone freezing technique for concentration of cesium and strontium elements was investigated. As a results of this research, only strontium was carbonated by reaction with Li 2 CO 3 (cesium did not react with Li 2 CO 3 ). In case of sulfate addition method, both cesium and strontium were converted into their sulfate that is Cs 2 S 2 O 6 and SrSO 4 and maximum sulfate efficiency of cesium and strontium were about 72% and 95%, respectively. Cesium and strontium involved in LiCl molten salt could be concentrated in the molten salt by using zone freezing method. (authors)

Evaluation of in-plant neutron coincidence counters for the measurement of molten salt extraction residues

International Nuclear Information System (INIS)

Langner, D.G.; Russo, P.A.; Wachter, J.R.

1993-01-01

Americium is extracted from plutonium by a molten salt extraction (MSE) process. The residual americium-laden salts are a significant waste stream in this pyrochemical purification process. Rapid assay of MSE residues is desirable to minimize the exposure of personnel to these often high-level emissions. However, the quantitative assay of plutonium in MSE residues is difficult. Variable, unknown (a,n) rates and variable emitted-neutron energy spectra preclude the use of standard neutron coincidence counting techniques with old-generation neutron coincidence counters. Gamma-ray assay methods have not been successful with some residues because of random lumps of plutonium metal. In this paper, we present measurements of MSE residues with two state-of-the-art neutron coincidence counters at the Los Alamos Plutonium Processing Facility: an in-line counter built for the assay of bulk waste material and the pyrochemical multiplicity counter that underwent test and evaluation at that facility. Both of these counters were designed to minimize the effects on measurements of variations in the sample geometry and variable energy spectra of emitted neutrons. These results are compared to measurements made with an HLNCII and with a 20-yr-old in-line well counter. The latter two counters are not optimized in ft sense. We conclude that the newer counters provide significantly improved assay results. The pyrochemical multiplicity counter operated in the conventional coincidence mode provided the best assays overall

Status of plutonium recycle from mixed oxide fuel fabrication wastes (U,Pu)O2 facility activities

International Nuclear Information System (INIS)

Quesada, Calixto A.; Adelfang, Pablo; Greiner, G.; Orlando, Oscar S.; Mathot, Sergio R.

1999-01-01

Within the specific subject of mixed oxides corresponding to the Fuel Cycle activities performed at CNEA, the recovery of plutonium from wastes originated during tests and pre-fabrication stages is performed. (author)

The uranium-plutonium breeder reactor fuel cycle

International Nuclear Information System (INIS)

Salmon, A.; Allardice, R.H.

1979-01-01

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

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.

Engineering Options Assessment Report. Nitrate Salt Waste Stream Processing

Energy Technology Data Exchange (ETDEWEB)

Anast, Kurt Roy [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

2015-11-13

This report examines and assesses the available systems and facilities considered for carrying out remediation activities on remediated nitrate salt (RNS) and unremediated nitrate salt (UNS) waste containers at Los Alamos National Laboratory (LANL). The assessment includes a review of the waste streams consisting of 60 RNS, 29 above-ground UNS, and 79 candidate below-ground UNS containers that may need remediation. The waste stream characteristics were examined along with the proposed treatment options identified in the Options Assessment Report . Two primary approaches were identified in the five candidate treatment options discussed in the Options Assessment Report: zeolite blending and cementation. Systems that could be used at LANL were examined for housing processing operations to remediate the RNS and UNS containers and for their viability to provide repackaging support for remaining LANL legacy waste.

Engineering Options Assessment Report: Nitrate Salt Waste Stream Processing

Energy Technology Data Exchange (ETDEWEB)

Anast, Kurt Roy [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

2015-11-18

This report examines and assesses the available systems and facilities considered for carrying out remediation activities on remediated nitrate salt (RNS) and unremediated nitrate salt (UNS) waste containers at Los Alamos National Laboratory (LANL). The assessment includes a review of the waste streams consisting of 60 RNS, 29 aboveground UNS, and 79 candidate belowground UNS containers that may need remediation. The waste stream characteristics were examined along with the proposed treatment options identified in the Options Assessment Report . Two primary approaches were identified in the five candidate treatment options discussed in the Options Assessment Report: zeolite blending and cementation. Systems that could be used at LANL were examined for housing processing operations to remediate the RNS and UNS containers and for their viability to provide repackaging support for remaining LANL legacy waste.

Formation, characterization, and stability of plutonium (IV) colloid

International Nuclear Information System (INIS)

Hobart, D.E.; Morris, D.E.; Palmer, P.D.; Newton, T.W.

1989-01-01

Plutonium is expected to be a major component of the waste element package in any high-level nuclear waste repository. Plutonium(IV) is known to form colloids under chemical conditions similar to those found in typical groundwaters. In the event of a breach of a repository, these colloids represent a source of radionuclide transport to the far-field environment, in parallel with the transport of dissolved waste element species. In addition, the colloids may decompose or disaggregate into soluble ionic species. Thus, colloids represent an additional term in determining waste element solubility limits. A thorough characterization of the physical and chemical properties of these colloids under relevant conditions is essential to assess the concentration limits and transport mechanisms for the waste elements at the proposed Yucca Mountain Repository site. This report is concerned primarily with recent results obtained by the Yucca Mountain Project (YMP) Solubility Determination Task pertaining to the characterization of the structural and chemical properties of Pu(IV) colloid. Important results will be presented which provides further evidence that colloidal plutonium(IV) is structurally similar to plutonium dioxide and that colloidal plutonium(IV) is electrochemically reactive. 13 refs., 7 figs

Radiolysis of Salts and Long-Term Storage Issues for Both Pure and Impure PuO{sub 2} Materials in Plutonium Storage Containers

Energy Technology Data Exchange (ETDEWEB)

Lav Tandon

2000-05-01

The Material Identification and Surveillance (MIS) project sponsored a literature search on the effects of radiation on salts, with focus on alkali chlorides. The goal of the survey was to provide a basis for estimating the magnitude of {alpha} radiation effects on alkali chlorides that can accompany plutonium oxide (PuO{sub 2}) into storage. Chloride radiolysis can yield potentially corrosive gases in plutonium storage containers that can adversely affect long-term stability. This literature search was primarily done to provide a tutorial on this topic, especially for personnel with nonradiation chemistry backgrounds.

Disposal of Surplus Weapons Grade Plutonium

International Nuclear Information System (INIS)

Alsaed, H.; Gottlieb, P.

2000-01-01

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

Alpha spectrum profiling of plutonium in leached simulated high-level radioactive waste-glass

International Nuclear Information System (INIS)

Diamond, H.; Friedman, A.M.

1981-01-01

Low-geometry X-ray spectra from /sup 239/Pu and /sup 237/Np, incorporated into simulated high-level radioactive waste-glass, were transformed into depth distributions for these elements. Changes in the depth profiles were observed for a series of static leachings in 75/degree/C water. Radiochemical assay of the leach solutions revealed that little neptunium or plutonium was leached, and that the amount leached was independent of leaching time. The depth profiles of the leached specimens showed that there was selective leaching of nonradioactive components of the glass, concentrating the remaining neptunium and plutonium in a broad zone near (but not at) the glass surface. Eventual redeposition of nonradioactive material onto the glass surface inhibited further leaching

Establishment of cooperation basis of joint research on the mixed waste molten salt oxidation technology

International Nuclear Information System (INIS)

Yang, Hee Chul; Cho, Y. J.; Kim, J. H.; Yoo, J. H.; Yun, H. C.; Lee, D. G.

2005-08-01

Molten salt oxidation, MSO for short, is a robust technology that can effectively treat mixed waste (radioactive waste including hazardous metals or organics). It can safely and economically treat the difficult wastes such as not-easily destroyable toxic organic waste, medical waste, chemical warfare and energetic materials such as propellant and explosives, all of which are not easily treated by an incinerator or other currently existing thermal treatment system. Therefore, molten salt oxidation technology should be developed and utilized to treat a lot of niche waste stored in the nuclear and environmental industries. So, if we put the MSO technology to practical use by Korea-Vietnam joint research, we can reduce R and D fund for MSO technology by ourselves and we can expect an export of the outcome of nuclear R and D in Korea. For Establishment of cooperation basis of joint research concerning molten salt oxidation technology between KOREA and VIETNAM, in this research, We invited two Vietnamese researchers and we introduced our experimental scale molten salt oxidation system in order to let them understand molten salt oxidation technology. We also visited Viet man and we consulted about molten salt oxidation process. We held seminar on the mixed waste molten salt oxidation technology, discussed on the joint research on the mixed waste molten salt oxidation technology and finally we wrote MOU for joint research

Establishment of cooperation basis of joint research on the mixed waste molten salt oxidation technology

Energy Technology Data Exchange (ETDEWEB)

Yang, Hee Chul; Cho, Y. J.; Kim, J. H.; Yoo, J. H.; Yun, H. C.; Lee, D. G

2005-08-01

Molten salt oxidation, MSO for short, is a robust technology that can effectively treat mixed waste (radioactive waste including hazardous metals or organics). It can safely and economically treat the difficult wastes such as not-easily destroyable toxic organic waste, medical waste, chemical warfare and energetic materials such as propellant and explosives, all of which are not easily treated by an incinerator or other currently existing thermal treatment system. Therefore, molten salt oxidation technology should be developed and utilized to treat a lot of niche waste stored in the nuclear and environmental industries. So, if we put the MSO technology to practical use by Korea-Vietnam joint research, we can reduce R and D fund for MSO technology by ourselves and we can expect an export of the outcome of nuclear R and D in Korea. For Establishment of cooperation basis of joint research concerning molten salt oxidation technology between KOREA and VIETNAM, in this research, We invited two Vietnamese researchers and we introduced our experimental scale molten salt oxidation system in order to let them understand molten salt oxidation technology. We also visited Viet man and we consulted about molten salt oxidation process. We held seminar on the mixed waste molten salt oxidation technology, discussed on the joint research on the mixed waste molten salt oxidation technology and finally we wrote MOU for joint research.

Radiolysis salt phenomenology: application to storage of high level radioactive waste

International Nuclear Information System (INIS)

Akram, Najib

1993-01-01

In France, rock salt is a candidate repository for highly radioactive waste. Rock salt contains water and adsorbed gases which can be released in boreholes after heating due to vitrified wastes. In addition, waste-induced irradiation in near-field conditions induce radiolytic reactions which also contribute to gas release. The aim of this work is to understand and evaluate the effects of heat and irradiation produced by waste containers in a deep disposal, primarily concerning gas production. This is justified by the impact of gases on long-term safety: toxicity, explosibility, chemical reactivity, pressure build-up. We have evidenced the influence of integrated dose, filling gases, temperature and grain size on an homogeneous medium (Asse Mine rock salt). We have then studied heterogeneous samples, which allowed to determine the influence of the chemical and mineralogical composition of rock salt (bedded rock salt from the Mine de Potasse d'Alsace). The role played by organic matter on gas production is important, leading for instance to high consumption rates of oxygen. Through this study, we have also considered the behaviour of clay-rich materials under irradiation. Our results constitute important bases for the future modelling of the phenomena which will take place in the near-field of a rock salt-type repository, especially concerning its long-term safety. (author) [fr

Technology for commercial radioactive waste management

International Nuclear Information System (INIS)

1979-05-01

A general analysis of transportation requirements for postfission radioactive wastes that are produced from the commercial light water reactor (LWR) fuel cycle and that are assumed to require Federal custody for storage or disposal is given. Possible radioactive wastes for which transportation requirements are described include: spent fuel, solidified high-level waste, fuel residues (cladding wastes), plutonium, and non-high-level transuranic (TRU) wastes. Transportation is described for wastes generated in three fuel cycle options: once-through fuel cycle, uranium recycle only, and recycle of uranium and plutonium. The geologic considerations essential for repository selection, the nature of geologic formations that are potential repository media, the thermal criteria for waste placement in geologic repositories, and conceptual repositories in four different geologic media are described. The media are salt deposits, granite, shale, and basalt. Possible alternatives for managing retired facilities and procedures for decommissioning are reviewed. A qualitative comparison is made of wastes generated by the uranium fuel cycle and the thorium fuel cycle. This study presents data characterizing wastes from prebreeder light water breeder reactors using thorium and slightly enriched uranium-235. The prebreeder LWBRs are essentially LWRs using thorium. The operation of HTGR and LWBR cycles are conceptually designed, and wastes produced in these cycles are compared for potential differences

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

Energy Technology Data Exchange (ETDEWEB)

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

1962-07-01

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

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

International Nuclear Information System (INIS)

Brault, J.R.

2000-01-01

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

Plutonium 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

Experimental results on salt concrete for barrier elements made of salt concrete in a repository for radioactive waste in a salt mine

International Nuclear Information System (INIS)

Gutsch, Alex-W.; Preuss, Juergen; Mauke, Ralf

2012-01-01

The Bartensleben rock salt mine in Germany was used as a repository for low and intermediate level radioactive waste from 1971 to 1991 and from 1994 to 1998. The repository with an overall volume of about 6 million m 3 has to be closed. Salt concrete is used for the refill of the voids of the repository. The concrete mixtures contain crushed salt instead of natural aggregates as the void filling material should be as similar to the salt rock as possible. Very high requirements regarding low heat development and little or even no cracking during concrete hardening had to be fulfilled even for the barrier elements made from salt concrete which separate the radioactive waste from the environment. Requirements for the salt concrete were set up with regard to the fluidity of the fresh concrete during the hardening process and its durability. In the view of a comprehensive numerical calculations of the temperature development and thermal stresses in the massive salt concrete elements of the backfill of the voids, experimental results for material properties of the salt concrete are presented: mixture of the salt concrete, thermodynamic properties (adiabatic heat release, thermal dilatation, thermal conductivity and heat capacity), mechanical short term properties, creep (under tension, under compression), autogenous shrinkage

Simulation of uranium and plutonium oxides compounds obtained in plasma

Science.gov (United States)

Novoselov, Ivan Yu.; Karengin, Alexander G.; Babaev, Renat G.

2018-03-01

The aim of this paper is to carry out thermodynamic simulation of mixed plutonium and uranium oxides compounds obtained after plasma treatment of plutonium and uranium nitrates and to determine optimal water-salt-organic mixture composition as well as conditions for their plasma treatment (temperature, air mass fraction). Authors conclude that it needs to complete the treatment of nitric solutions in form of water-salt-organic mixtures to guarantee energy saving obtainment of oxide compounds for mixed-oxide fuel and explain the choice of chemical composition of water-salt-organic mixture. It has been confirmed that temperature of 1200 °C is optimal to practice the process. Authors have demonstrated that condensed products after plasma treatment of water-salt-organic mixture contains targeted products (uranium and plutonium oxides) and gaseous products are environmental friendly. In conclusion basic operational modes for practicing the process are showed.

Treatment of plutonium-contaminated solid waste: a review of handling systems

International Nuclear Information System (INIS)

Meredith, B.E.; Hardy, A.R.

1985-02-01

Handling techniques are reviewed to identify those suitable for adaptation for use in transporting large items of redundant plutonium contaminated plant and equipment to a remotely operated size reduction facility, moving them into the facility, presenting them to size reduction equipment and loading the processed waste into drums. It is concluded that an integrated system based on a combination of slatted conveyors, roller tables, air transporters and manipulators, merits further consideration. An appropriate experimental programme is outlined. (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

Effects Influencing Plutonium-Absorber Interactions and Distributions in Routine and Upset Waste Treatment Plant Operations

Energy Technology Data Exchange (ETDEWEB)

Delegard, Calvin H. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Sinkov, Sergey I. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Fiskum, Sandra K. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2015-05-01

This report is the third in a series of analyses written in support of a plan to revise the Hanford Waste Treatment and Immobilization Plant (WTP) Preliminary Criticality Safety Evaluation Report (CSER) that is being implemented at the request of the U.S. Department of Energy (DOE) Criticality Safety Group. A report on the chemical disposition of plutonium in Hanford tank wastes was prepared as Phase 1 of this plan (Delegard and Jones 2015). Phase 2 is the provision of a chemistry report to describe the potential impacts on criticality safety of waste processing operations within the WTP (Freer 2014). In accordance with the request from the Environmental and Nuclear Safety Department of the WTP (Miles and Losey 2012), the Phase 2 report assessed the potential for WTP process conditions within and outside the range of normal control parameters to change the ratio of fissile material to neutron-absorbing material in the waste as it is processed with an eye towards potential implications for criticality safety. The Phase 2 study also considered the implications should WTP processes take place within the credible range of chemistry upset conditions. In the present Phase 3 report, the 28 phenomena described in the Phase 2 report were considered with respect to the disposition of plutonium and various absorber elements. The phenomena identified in the Phase 2 report are evaluated in light of the Phase 1 report and other resources to determine the impacts these phenomena might have to alter the plutonium/absorber dispositions and ratios. The outcomes of the Phase 3 evaluations then can be used to inform subsequent engineering decisions and provide reasonable paths forward to mitigate or overcome real or potential criticality concern in plant operations.

Precipitation of plutonium from acidic solutions using magnesium oxide

International Nuclear Information System (INIS)

Jones, S.A.

1994-01-01

Plutonium (IV) is only marginally soluble in alkaline solution. Precipitation of plutonium using sodium or potassium hydroxide to neutralize acidic solutions produces a gelatinous solid that is difficult to filter and an endpoint that is difficult to control. If the pH of the solution is too high, additional species precipitate producing an increased volume of solids separated. The use of magnesium oxide as a reagent has advantages. It is added as a solid (volume of liquid waste produced is minimized), the pH is self-limiting (pH does not exceed about 8.5), and the solids precipitated are more granular (larger particle size) than those produced using KOH or NaOH. Following precipitation, the raffinate is expected to meet criteria for disposal to tank farms. The solid will be heated in a furnace to dry it and convert any hydroxide salts to the oxide form. The material will be cooled in a desiccator. The material is expected to meet vault storage criteria

Test plan for immobilization of salt-containing surrogate mixed wastes using polyester resins

International Nuclear Information System (INIS)

Biyani, R.K.; Douglas, J.C.; Hendrickson, D.W.

1997-01-01

Past operations at many Department of Energy (DOE) sites have resulted in the generation of several waste streams with high salt content. These wastes contain listed and characteristic hazardous constituents and are radioactive. The salts contained in the wastes are primarily chloride, sulfate, nitrate, metal oxides, and hydroxides. DOE has placed these types of wastes under the purview of the Mixed Waste Focus Area (MWFA). The MWFA has been tasked with developing and facilitating the implementation of technologies to treat these wastes in support of customer needs and requirements. The MWFA has developed a Technology Development Requirements Document (TDRD), which specifies performance requirements for technology owners and developers to use as a framework in developing effective waste treatment solutions. This project will demonstrate the use of polyester resins in encapsulating and solidifying DOE's mixed wastes containing salts, as an alternative to conventional and other emerging immobilization technologies

Test plan for immobilization of salt-containing surrogate mixed wastes using polyester resins

Energy Technology Data Exchange (ETDEWEB)

Biyani, R.K.; Douglas, J.C.; Hendrickson, D.W.

1997-07-07

Past operations at many Department of Energy (DOE) sites have resulted in the generation of several waste streams with high salt content. These wastes contain listed and characteristic hazardous constituents and are radioactive. The salts contained in the wastes are primarily chloride, sulfate, nitrate, metal oxides, and hydroxides. DOE has placed these types of wastes under the purview of the Mixed Waste Focus Area (MWFA). The MWFA has been tasked with developing and facilitating the implementation of technologies to treat these wastes in support of customer needs and requirements. The MWFA has developed a Technology Development Requirements Document (TDRD), which specifies performance requirements for technology owners and developers to use as a framework in developing effective waste treatment solutions. This project will demonstrate the use of polyester resins in encapsulating and solidifying DOE`s mixed wastes containing salts, as an alternative to conventional and other emerging immobilization technologies.

Waste isolation facility description: bedded salt

Energy Technology Data Exchange (ETDEWEB)

1976-09-01

The waste isolation facility is designed to receive and store three basic types of solidified wastes: high-level wastes, intermediate level high-gamma transuranic waste, and low-gamma transuranic wastes. The facility under consideration in this report is designed for bedded salt at a depth of approximately 1800 ft. The present design for the facility includes an area which would be used initially as a pilot facility to test the viability of the concept, and a larger facility which would constitute the final storage area. The total storage area in the pilot facility is planned to be 77 acres and in the fuel facility 1601 acres. Other areas for shaft operations and access would raise the overall size of the total facility to slightly less than 2,000 acres. The following subjects are discussed in detail: surface facilities, shaft design and characteristics, design and construction of the underground waste isolation facility, ventilation systems, and design requirements and criteria. (LK)

Waste isolation facility description: bedded salt

International Nuclear Information System (INIS)

1976-09-01

The waste isolation facility is designed to receive and store three basic types of solidified wastes: high-level wastes, intermediate level high-gamma transuranic waste, and low-gamma transuranic wastes. The facility under consideration in this report is designed for bedded salt at a depth of approximately 1800 ft. The present design for the facility includes an area which would be used initially as a pilot facility to test the viability of the concept, and a larger facility which would constitute the final storage area. The total storage area in the pilot facility is planned to be 77 acres and in the fuel facility 1601 acres. Other areas for shaft operations and access would raise the overall size of the total facility to slightly less than 2,000 acres. The following subjects are discussed in detail: surface facilities, shaft design and characteristics, design and construction of the underground waste isolation facility, ventilation systems, and design requirements and criteria

Plutonium recovery from spent reactor fuel by uranium displacement

Science.gov (United States)

Ackerman, J.P.

1992-03-17

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

Plutonium recovery from spent reactor fuel by uranium displacement

International Nuclear Information System (INIS)

Ackerman, J.P.

1992-01-01

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

Different Methods for Conditioning Chloride Salt Wastes

International Nuclear Information System (INIS)

De Angelis, G.; Fedeli, C.; Capone, M.; Marzo, G.A.; Mariani, M.; Da Ros, M.; Giacobbo, F.; Macerata, E.; Giola, M.

2015-01-01

Three different methods have been used to condition chloride salt wastes coming from pyro-processes. Two of them allow to synthesise sodalite, a naturally occurring mineral containing chlorine: the former, starting from Zeolite 4A, which transforms the zeolite into sodalite; the latter, which starts from kaolinite, giving sodalite as well. In addition, a new matrix, termed SAP (SiO 2 -Al 2 O 3 -P 2 O 5 ), has been synthesised. It is able to form different mineral phases which occlude fission metals. The products from the different processes have been fully characterised. In particular the chemical durability of the final waste forms has been determined using the standard product consistency test. According to the results obtained, SAP seems to be a promising matrix for the incorporation of chloride salt wastes from pyro-processes. Financial support from the Nuclear Fission Safety Programme of the European Union (projects ACSEPT, contract FP7-CP-2007- 211 267, and SACSESS, Collaborative Project 323282), as well as from Italian Ministry for Economic Development (Accordo di Programma: Piano Annuale di Realizzazione 2008-2009) is gratefully acknowledged. (authors)

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

Processes and parameters involved in modeling radionuclide transport from bedded salt repositories. Final report. Technical memorandum

International Nuclear Information System (INIS)

Evenson, D.E.; Prickett, T.A.; Showalter, P.A.

1979-07-01

The parameters necessary to model radionuclide transport in salt beds are identified and described. A proposed plan for disposal of the radioactive wastes generated by nuclear power plants is to store waste canisters in repository sites contained in stable salt formations approximately 600 meters below the ground surface. Among the principal radioactive wastes contained in these canisters will be radioactive isotopes of neptunium, americium, uranium, and plutonium along with many highly radioactive fission products. A concern with this form of waste disposal is the possibility of ground-water flow occurring in the salt beds and endangering water supplies and the public health. Specifically, the research investigated the processes involved in the movement of radioactive wastes from the repository site by groundwater flow. Since the radioactive waste canisters also generate heat, temperature is an important factor. Among the processes affecting movement of radioactive wastes from a repository site in a salt bed are thermal conduction, groundwater movement, ion exchange, radioactive decay, dissolution and precipitation of salt, dispersion and diffusion, adsorption, and thermomigration. In addition, structural changes in the salt beds as a result of temperature changes are important. Based upon the half-lives of the radioactive wastes, he period of concern is on the order of a million years. As a result, major geologic phenomena that could affect both the salt bed and groundwater flow in the salt beds was considered. These phenomena include items such as volcanism, faulting, erosion, glaciation, and the impact of meteorites. CDM reviewed all of the critical processes involved in regional groundwater movement of radioactive wastes and identified and described the parameters that must be included to mathematically model their behavior. In addition, CDM briefly reviewed available echniques to measure these parameters

Stabilization of plutonium bearing residues at Lawrence Livermore National Laboratory

International Nuclear Information System (INIS)

Bronson, M.C.; Van Konynenburg, R.A.; Ebbinghaus, B.B.

1995-01-01

The US Department of Energy's (US DOE) Lawrence Livermore National Laboratory (LLNL) has plutonium holdings including metal, oxide and residue materials, all of which need stabilization of some type. Residue materials include calcined ash, calcined precipitates, pyrochemical salts, glove box sweepings, metallurgical samples, graphite, and pyrochemical ceramic crucibles. These residues are typical of residues stored throughout the US DOE plutonium sites. The stabilization process selected for each of these residues requires data on chemical impurities, physical attributes, and chemical forms of the plutonium. This paper outlines the characterization and stabilization of LLNL ash residues, pyrochemical salts, and graphite

In Plant Measurement and Analysis of Mixtures of Uranium and Plutonium TRU-Waste Using a 252Cf Shuffler Instrument

International Nuclear Information System (INIS)

Hurd, J.R.

1998-01-01

The active-passive 252 Cf shuffler instrument, installed and certified several years ago in Los Alamos National Laboratory's plutonium facility, has now been calibrated for different matrices to measure Waste Isolation Pilot Plant (WIPP)-destined transuranic (TRU)-waste. Little or no data currently exist for these types of measurements in plant environments where sudden large changes in the neutron background radiation can significantly distort the results. Measurements and analyses of twenty-two 55-gallon drums, consisting of mixtures of varying quantities of uranium and plutonium in mostly noncombustible matrices, have been recently completed at the plutonium facility. The calibration and measurement techniques, including the method used to separate out the plutonium component, will be presented and discussed. Calculations used to adjust for differences in uranium enrichment from that of the calibration standards will be shown. Methods used to determine various sources of both random and systematic error will be indicated. Particular attention will be directed to those problems identified as arising from the plant environment. The results of studies to quantify the aforementioned distortion effects in the data will be presented. Various solution scenarios will be outlined, along with those adopted here

Concepts and Technologies for Radioactive Waste Disposal in Rock Salt

Directory of Open Access Journals (Sweden)

Wernt Brewitz

2007-01-01

Full Text Available In Germany, rock salt was selected to host a repository for radioactive waste because of its excellent mechanical properties. During 12 years of practical disposal operation in the Asse mine and 25 years of disposal in the disused former salt mine Morsleben, it was demonstrated that low-level wastes (LLW and intermediate-level wastes (ILW can be safely handled and economically disposed of in salt repositories without a great technical effort. LLW drums were stacked in old mining chambers by loading vehicles or emplaced by means of the dumping technique. Generally, the remaining voids were backfilled by crushed salt or brown coal filter ash. ILW were lowered into inaccessible chambers through a borehole from a loading station above using a remote control.Additionally, an in-situ solidification of liquid LLW was applied in the Morsleben mine. Concepts and techniques for the disposal of heat generating high-level waste (HLW are advanced as well. The feasibility of both borehole and drift disposal concepts have been proved by about 30 years of testing in the Asse mine. Since 1980s, several full-scale in-situ tests were conducted for simulating the borehole emplacement of vitrified HLW canisters and the drift emplacement of spent fuel in Pollux casks. Since 1979, the Gorleben salt dome has been investigated to prove its suitability to host the national final repository for all types of radioactive waste. The “Concept Repository Gorleben” disposal concepts and techniques for LLW and ILW are widely based on the successful test operations performed at Asse. Full-scale experiments including the development and testing of adequate transport and emplacement systems for HLW, however, are still pending. General discussions on the retrievability and the reversibility are going on.

Pyrolytic conversion of plastic and rubber waste to hydrocarbons with basic salt catalysts

Science.gov (United States)

Wingfield, Jr., Robert C.; Braslaw, Jacob; Gealer, Roy L.

1985-01-01

The invention relates to a process for improving the pyrolytic conversion of waste selected from rubber and plastic to low molecular weight olefinic materials by employing basis salt catalysts in the waste mixture. The salts comprise alkali or alkaline earth compounds, particularly sodium carbonate, in an amount of greater than about 1 weight percent based on the waste feed.

Potential for creation of a salt dome following disposal of radioactive waste in a salt layer

International Nuclear Information System (INIS)

Fries, G.

1987-01-01

The study aims at quantifying the possibility of creation of a salt dome from a salt layer in which heat-emitting radioactive waste would be buried. Volume 1 describes the results of numerical computer simulations, and of laboratory-scale models in centrifuges. Volume 2 envisages, in a geological perspective, the origin of salt domes, the mechanisms of thei formation, and the associated parameters [fr

Potential for creation of a salt dome following disposal of radioactive waste in a salt layer

International Nuclear Information System (INIS)

Charo, L.; Habib, P.

1987-01-01

The study aims at quantifying the possibility of creation of a salt dome from a salt layer in which heat-emitting radioactive waste would be buried. Volume 1 describes the results of numerical computer simulations, and of laboratory-scale models in centrifuges. Volume 2 envisages, in a geological perspective, the origin of salt domes, the mechanisms of their formation, and the associated parameters [fr

The use of absorption spectroscopy of plutonium to minimize waste streams

International Nuclear Information System (INIS)

Vaughn, R.B.; Berg, J.; Cisneros, M.

1997-01-01

Through the use of absorption spectroscopy we are better able to understand the chemical reactions of plutonium and other actinide elements in solution. In many cases such an understanding can minimize the generation of waste streams by suggesting more optimal chemical conditions for separating these radioactive elements from their host matrix. Many processes are developed using an empirical approach with little understanding of what is actually taking place. One such example is the anion exchange process for Plutonium purification. Various resins have been tested in various solutions and workable outcomes have been produced. However, absorption spectroscopy provides an understanding of why ion exchange works and can determine which compounds complex best with actinides in order to obtain a more efficient and effective separations process. This presentation will touch on the chemistry involved, the spectroscopic instrumentation, and the environmental impacts. Primarily the talk will focus on the chemical technicians involvement in the day to day research, the obstacles encountered, and the environment in which this research was conducted

Waste salt disposal at the Savannah River Plant

International Nuclear Information System (INIS)

Langton, C.A.; Oblath, S.B.; Pepper, D.W.; Wilhite, E.L.

1986-01-01

Waste salt solution, produced during processing of high-level nuclear waste, will be incorporated in a cement matrix for emplacement in an engineered disposal facility. Wasteform characteristics and disposal facility details will be presented along with results of a field test of wasteform contaminant release and of modeling studies to predict releases. 5 refs., 11 figs., 5 tabs

Waste package for a repository located in salt

International Nuclear Information System (INIS)

Basham, S.J. Jr.

1983-01-01

This paper describes the current status of the waste package designs for salt repositories. The status of the supporting studies of environment definition, corrosion of containment materials, and leaching of waste forms is also presented. Emphasis is on the results obtained in FY 83 and the planned effort in FY 84. 8 references, 3 figures, 1 table

Recovery of fissile materials from plutonium residues, miscellaneous spent nuclear fuel, and uranium fissile wastes

International Nuclear Information System (INIS)

Forsberg, C.W.

1997-01-01

A new process is proposed that converts complex feeds containing fissile materials into a chemical form that allows the use of existing technologies (such as PUREX and ion exchange) to recover the fissile materials and convert the resultant wastes to glass. Potential feed materials include (1) plutonium scrap and residue, (2) miscellaneous spent nuclear fuel, and (3) uranium fissile wastes. The initial feed materials may contain mixtures of metals, ceramics, amorphous solids, halides, and organics. 14 refs., 4 figs

Plutonium immobilization program - Cold pour Phase 1 test results

International Nuclear Information System (INIS)

Hamilton, L.

2000-01-01

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

Plutonium Immobilization Program - Cold pour Phase 1 test results

International Nuclear Information System (INIS)

Hamilton, L.

2000-01-01

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

Americium Separations from High-Salt Solutions Using Anion Exchange

International Nuclear Information System (INIS)

Barr, Mary E.; Jarvinen, Gordon D.; Stark, Peter C.; Chamberlin, Rebecca M.; Bartsch, Richard A.; Zhang, Z.Y.; Zhao, W.

2001-01-01

The aging of the US nuclear stockpile presents a number of challenges, including the increasing radioactivity of plutonium residues due to the ingrowth of 241 Am from the β-decay of 241 Pu. We investigated parameters that affect the sorption of Am onto anion-exchange resins from concentrated effluents derived from nitric acid processing of plutonium residues. These postevaporator wastes are nearly saturated solutions of acidic nitrate salts, and americium removal is complicated by physical factors, such as solution viscosity and particulates, as well as by the presence of large quantities of competing metals and acid. Single- and double-contact batch distribution coefficients for americium and neodymium from simple and complex surrogate solutions are presented. Varied parameters include the nitrate salt concentration and composition and the nitric acid concentration. We find that under these extremely concentrated conditions, Am(III) removal efficiencies can surpass 50% per contact. Distribution coefficients for both neodymium and americium are insensitive to solution acidity and appear to be driven primarily by low water activities of the solutions

Treatment of waste salt from the advanced spent fuel conditioning process (II) : optimum immobilization condition

International Nuclear Information System (INIS)

Kim, Jeong Guk; Lee, Jae Hee; Yoo, Jae Hyung; Kim, Joon Hyung

2004-01-01

Since zeolite is known to be stable at a high temperature, it has been reported as a promising immobilization matrix for waste salt. The crystal structure of dehydrated zeolite A breaks down above 1060 K, resulting in the formation of an amorphous solid and re-crystallization to beta-Cristobalite. This structural degradation depends on the existence of chlorides. When contacted to HCl, zeolite 4A is not stable even at 473 K. The optimum consolidation condition for LiCl salt waste from the oxide fuel reduction process based on the electrochemical method (Advanced spent fuel Conditioning Process; ACP) has been studied using zeolite A since 2001. Actually the constituents of waste salt are water-soluble. And, alkali halides are known to be readily radiolyzed to yield interstitial halogens and metal colloids. For disposal in a geological repository, the waste salt must meet the acceptance criteria. For a waste form containing chloride salt, two of the more important criteria are leach resistance and waste form durability. In this work, we prepared some samples with different mixing ratios of LiCl salt to zeolite A, and then compared some characteristics such as thermal stability, salt occlusion, free chloride content, leach resistance, mixing effect, etc

Plutonium immobilization in glass and ceramics

Energy Technology Data Exchange (ETDEWEB)

Knecht, D.A. [Lockheed Martin Idaho Technologies, Idaho Falls (United States); Murphy, W.M. [Southwest Research Institute, San Antonio, TX (United States)

1996-05-01

The Materials Research Society Nineteenth Annual Symposium on the Scientific Basis for Nuclear Waste Management was held in Boston on November 27 to December 1, 1995. Over 150 papers were presented at the Symposium dealing with all aspects of nuclear waste management and disposal. Fourteen oral sessions and on poster session included a Plenary session on surplus plutonium dispositioning and waste forms. The proceedings, to be published in April, 1996, will provide a highly respected, referred compilation of the state of scientific development in the field of nuclear waste management. This paper provides a brief overview of the selected Symposium papers that are applicable to plutonium immobilization and plutonium waste form performance. Waste forms that were described at the Symposium cover most of the candidate Pu immobilization options under consideration, including borosilicate glass with a melting temperature of 1150 {degrees}C, a higher temperature (1450 {degrees}C) lanthanide glass, single phase ceramics, multi-phase ceramics, and multi-phase crystal-glass composites (glass-ceramics or slags). These Symposium papers selected for this overview provide the current status of the technology in these areas and give references to the relevant literature.

Plutonium immobilization in glass and ceramics

International Nuclear Information System (INIS)

Knecht, D.A.; Murphy, W.M.

1996-01-01

The Materials Research Society Nineteenth Annual Symposium on the Scientific Basis for Nuclear Waste Management was held in Boston on November 27 to December 1, 1995. Over 150 papers were presented at the Symposium dealing with all aspects of nuclear waste management and disposal. Fourteen oral sessions and on poster session included a Plenary session on surplus plutonium dispositioning and waste forms. The proceedings, to be published in April, 1996, will provide a highly respected, referred compilation of the state of scientific development in the field of nuclear waste management. This paper provides a brief overview of the selected Symposium papers that are applicable to plutonium immobilization and plutonium waste form performance. Waste forms that were described at the Symposium cover most of the candidate Pu immobilization options under consideration, including borosilicate glass with a melting temperature of 1150 degrees C, a higher temperature (1450 degrees C) lanthanide glass, single phase ceramics, multi-phase ceramics, and multi-phase crystal-glass composites (glass-ceramics or slags). These Symposium papers selected for this overview provide the current status of the technology in these areas and give references to the relevant literature

Immobilization of IFR salt wastes in mortar

International Nuclear Information System (INIS)

Fisher, D.F.; Johnson, T.R.

1988-01-01

Portland cement-base mortars are being considered for immobilizing chloride salt wastes from the fuel cycle of an integral fast reactor (IFR). The IFR is a sodium-cooled fast reactor with metal fuel. It has a close-coupled fuel cycle in which fission products are separated from the actinides in an electrochemical cell operating at 500 degrees C. This cell has a cadmium anode and a liquid salt electrolyte. The salt will be a low-melting mixture of alkaline and alkaline earth chlorides. This paper discusses one method being considered for immobilizing this treated salt, to disperse it in a portland cement-base motar, which would then be sealed in corrosion-resistant containers. For this application, the grout must be sufficiently fluid that it can be pumped into canisters where it will solidify into a strong, leach-resistant material

Plutonium in the aquatic environment around the Rocky Flats facility

International Nuclear Information System (INIS)

Thompson, M.A.

1975-01-01

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

Cerebral salt wasting following tuberculous meningoencephalitis in an infant

Directory of Open Access Journals (Sweden)

Syed Ahmed Zaki

2012-01-01

Full Text Available In patients with central nervous system disease, life-threatening hyponatremia can result from either the syndrome of inappropriate secretion of antidiuretic hormone or cerebral salt wasting. Clinical manifestations of the two conditions may be similar, but their pathogeneses and management protocols are different. Cerebral salt wasting syndrome is a disorder in which excessive natriuresis and hyponatremia occurs in patients with intracranial diseases. We report a 6-month-old girl with CSWS associated with tuberculous meningoencephalitis. She was diagnosed as having CSWS on the basis of hypovolemia, polyuria, natriuresis, and the relatively high level of fractional excretion of uric acid. Aggressive replacement of urine salt and water losses using 0.9% or 3% sodium chloride was done. Fludrocortisone was started at 0.1 mg twice daily on the seventh day of admission and was continued for 17 days.

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

International Nuclear Information System (INIS)

Pillay, K.K.S.

1994-02-01

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

Destruction of high explosives and wastes containing high explosives using the molten salt destruction process

International Nuclear Information System (INIS)

Upadhye, R.S.; Brummond, W.A.; Pruneda, C.O.

1992-01-01

This paper reports the Molten Salt Destruction (MSD) Process which has been demonstrated for the destruction of HE and HE-containing wastes. MSD has been used by Rockwell International and by Anti-Pollution Systems to destroy hazardous wastes. MSD converts the organic constituents (including the HE) of the waste into non-hazardous substances such as carbon dioxide, nitrogen and water. In the case of HE-containing mixed wastes, any actinides in the waste are retained in the molten salt, thus converting the mixed wastes into low-level wastes. (Even though the MSD process is applicable to mixed wastes, this paper will emphasize HE-treatment.) The destruction of HE is accomplished by introducing it, together with oxidant gases, into a crucible containing a molten salt, such as sodium carbonate, or a suitable mixture of the carbonates of sodium, potassium, lithium and calcium. The temperature of the molten salt can be between 400 to 900 degrees C. The combustible organic components of the waste react with oxygen to produce carbon dioxide, nitrogen and steam

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.

A vision for environmentally conscious plutonium processing

International Nuclear Information System (INIS)

Avens, L.R.; Eller, P.G.; Christensen, D.C.; Miller, W.L.

1998-01-01

Regardless of individual technical and political opinions about the uses of plutonium, it is virtually certain that plutonium processing will continue on a significant global scale for many decades for the purposes of national defense, nuclear power, and remediation. An unavoidable aspect of plutonium processing is that radioactively contaminated gas, liquid, and solid waste streams are generated. These streams need to be handled in a manner that not only is in full compliance with today's laws but also will be considered environmentally and economically responsible now and in the future. In this regard, it is indeed ironic that the multibillion dollar and multidecade radioactive cleanup mortgage that the US Department of Energy (and its Russian counterpart) now owns resulted from waste management practices that were at the time in full legal compliance. It is now abundantly evident that in the long run, these practices have proven to be neither environmentally nor economically sound. Recent dramatic advances in actinide science and technology now make it possible to drastically minimize or even eliminate the problematic waste streams of traditional plutonium processing operations. Advanced technology thereby provides the means to avoid passing on to children and grandchildren significant environmental and economic legacies that traditional processing inevitably produces. The authors describe such a vision for plutonium processing that could be implemented fully within 5 yr at a facility such as the Los Alamos National Laboratory Plutonium Facility (TA55). As a significant bonus, even on this short timescale, the initial technology investment is handsomely returned in avoided waste management costs

Salt-occluded zeolite waste forms: Crystal structures and transformability

International Nuclear Information System (INIS)

Richardson, J.W. Jr.

1996-01-01

Neutron diffraction studies of salt-occluded zeolite and zeolite/glass composite samples, simulating nuclear waste forms loaded with fission products, have revealed complex structures, with cations assuming the dual roles of charge compensation and occlusion (cluster formation). These clusters roughly fill the 6--8 angstrom diameter pores of the zeolites. Samples are prepared by equilibrating zeolite-A with complex molten Li, K, Cs, Sr, Ba, Y chloride salts, with compositions representative of anticipated waste systems. Samples prepared using zeolite 4A (which contains exclusively sodium cations) as starting material are observed to transform to sodalite, a denser aluminosilicate framework structure, while those prepared using zeolite 5A (sodium and calcium ions) more readily retain the zeolite-A structure. Because the sodalite framework pores are much smaller than those of zeolite-A, clusters are smaller and more rigorously confined, with a correspondingly lower capacity for waste containment. Details of the sodalite structures resulting from transformation of zeolite-A depend upon the precise composition of the original mixture. The enhanced resistance of salt-occluded zeolites prepared from zeolite 5A to sodalite transformation is thought to be related to differences in the complex chloride clusters present in these zeolite mixtures. Data relating processing conditions to resulting zeolite composition and structure can be used in the selection of processing parameters which lead to optimal waste forms

Challenges using a 252Cf shuffler instrument in a plant environment to measure mixtures of uranium and plutonium transuranic waste

International Nuclear Information System (INIS)

Hurd, J.R.

1999-01-01

An active-passive 252 Cf shuffler instrument, installed and certified several years ago at Los Alamos National Laboratory's plutonium facility, has now been calibrated for different matrices to measure Waste Isolation Pilot Plant (WIPP)-destined transuranic (TRU) waste. Little or no data currently exist for these types of measurements in plant environments where sudden large changes in the neutron background radiation can significantly distort the results. Measurements and analyses of twenty-two 55-gallon drums, consisting of mixtures of varying quantities of uranium and plutonium in mostly noncombustible matrices, have been recently completed at the plutonium facility. The calibration and measurement techniques, including the method used to separate out the plutonium component, will be presented and discussed. Calculations used to adjust for differences in uranium enrichment from that of the calibration standards will be shown. Methods used to determine various sources of both random and systematic error will be indicated. Particular attention will be directed to those problems identified as arising from the plant environment. The results of studies to quantify the aforementioned distortion effects in the data will be presented. Various solution scenarios will be outlined, along with those adopted here

Nuclear waste in sea or salt? No, wrong

International Nuclear Information System (INIS)

Damveld, H.; Van Duin, S.; Bannink, D.

1994-04-01

Eighteen years of successful action against ocean dumping and storage of nuclear waste in salt domes are reviewed for the Dutch situation. The aim of this book is to hand some support to those who want to act against trial borings, in particular the people living close to the most important salt domes in the Netherlands: Ternaard, Zuidwending, Pieterburen, Onstwedde, Winschoten, Schoonlo and Gasselte-Drouwen. In 1976 the Interdepartmental Commission on Nuclear Energy with its subcommission Radioactive Substances (ICK-RAS) was installed, along with a number of working groups, responsible for research. From 1978 onwards ocean dumping operations were accompanied by blockades and legal procedures, which led to a situation of the last dumping in 1982. The Dutch government then focused on nuclear waste storage in salt domes for which the OPLA research program was started. OPLA is the Dutch abbreviation for Storage on Land. The final report (phase 1 and 1a) of OPLA was published on 15 October 1993 as annex to the Dossier Nuclear Energy of the Dutch government. It has been decided that phase 1a is not followed by trial drillings, as planned before. Some critical remarks are made regarding the rounds of public participation and the notion of permanent retrievability of stored nuclear waste. Extensive use has been made of documentation from the Dutch government and parliament, and other literature and information sources

Temperature distributions in a salt formation used for the ultimate disposal of high-level radioactive waste

International Nuclear Information System (INIS)

Ploumen, P.

1980-01-01

In the Federal Republic of Germany the works on waste disposal is focussed on the utilization of a salt formation for ultimate disposal of radioactive wastes. Heat released from the high-level waste will be dissipated in the salt and the surrounding geologic formations. The occuring temperature distributions will be calculated with computer codes. A survey of the developed computer codes will be shown; the results for a selected example, taking into account the loading sequence of the waste, the mine ventilation as well as an air gap between the waste and the salt, will be discussed. Furthermore it will be shown that by varying the disposal parameters, the maximum salt temperature can be below any described value. (Auth.)

Radiological consequences associated with human intrusion into radioactive waste repositories in salt formations

International Nuclear Information System (INIS)

Jacquier, P.

1989-01-01

The assessment of the radiological impact of human intrusion scenarios is extremely important in the case of repositories located in salt formations, since salt is obviously a valuable economic resource. Salt formations also represent a suitable medium for mining storage caverns for oil and gas. The scenario considered in this report is that of solution mining in salt formations to produce salt for human consumption. It is postulated that the salt is extracted by excavating a cavern through solution-mining and that, in the course of cavern enlargement, the waste is intercepted and drops to the bottom of the cavern. We have assumed that the intrusion takes place 500 or even 2 500 years after the repository has been sealed. The cases considered involve high-level vitrified waste or cemented alpha waste. The paper describes the assumptions on which the scenario is based and uses a simplified model to assess the radiological consequences associated with the ingestion of contaminated salt. The paper also provides details of a sensitivity/uncertainty analysis which identified several areas in which experimental studies should be either initiated or continued [fr

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

Development and characterization of new high-level waste form containing LiCl KCl eutectic salts for achieving waste minimization from pyroprocessing

International Nuclear Information System (INIS)

Cho, Yong Zun; Kim, In Tae; Park, Hwan Seo; Ahn, Byeung Gil; Eun, Hee Chul; Son, Seock Mo; Ah, Su Na

2011-12-01

The purpose of this project is to develop new high level waste (HLW) forms and fabrication processes to dispose of active metal fission products that are removed from electrorefiner salts in the pyroprocessing based fuel cycle. The current technology for disposing of active metal fission products in pyroprocessing involves non selectively discarding of fission product loaded salt in a glass-bonded sodalite ceramic waste form. Selective removal of fission products from the molten salt would greatly minimize the amount of HLW generated and methods were developed to achieve selective separation of fission products during a previous I NERI research project (I NERI 2006 002 K). This I NERI project proceeds from the previous project with the development of suitable waste forms to immobilize the separated fission products. The Korea Atomic Energy Research Institute (KAERI) has focused primarily on developing these waste forms using surrogate waste materials, while the Idaho National Laboratory (INL) has demonstrated fabrication of these waste forms using radioactive electrorefiner salts in hot cell facilities available at INL. Testing and characterization of these radioactive materials was also performed to determine the physical, chemical, and durability properties of the waste forms

Modeling of waste/near field interactions for a waste repository in bedded salt: the Dynamic Network (DNET) model

International Nuclear Information System (INIS)

Cranwell, R.M.

1983-01-01

The Fuel Cycle Risk Analysis Division of Sandia National Laboratories has been funded by the US Nuclear Regulatory Commission to develop a methodology for use in assessing the long-term risk from the disposal of radioactive wastes in deep geologic formations. As part of this program, the Dynamic Network (DNET) model was developed to investigate waste/near field interactions associated with the disposal of radioactive wastes in bedded salt formations. The model is a quasi-multi-dimensional network model with capabilities for simulating processes such as fluid flow, heat transport, salt dissolution, salt creep, and the effects of thermal expansion and subsedence on the rock units surrounding the repository. The use of DNET has been demonstrated in the analysis of a hypothetical disposal site containing a bedded salt formation as the host medium for the repository. An example of this demonstration analysis is discussed. Furthermore, the outcome of sensitivity analyses performed on the DNET model are presented

Interim performance specifications for conceptual waste-package designs for geologic isolation in salt repositories

International Nuclear Information System (INIS)

1983-06-01

The interim performance specifications and data requirements presented apply to conceptual waste package designs for all waste forms which will be isolated in salt geologic repositories. The waste package performance specifications and data requirements respond to the waste package performance criteria. Subject areas treated include: containment and controlled release, operational period safety, criticality control, identification, and waste package performance testing requirements. This document was generated for use in the development of conceptual waste package designs in salt. It will be revised as additional data, analyses, and regulatory requirements become available

Crystallization of sodium nitrate from radioactive waste

International Nuclear Information System (INIS)

Krapukhin, V.B.; Krasavina, E.P.; Pikaev, A.K.

1997-07-01

From the 1940s to the 1980s, the Institute of Physical Chemistry of the Russian Academy of Sciences (IPC/RAS) conducted research and development on processes to separate acetate and nitrate salts and acetic acid from radioactive wastes by crystallization. The research objective was to decrease waste volumes and produce the separated decontaminated materials for recycle. This report presents an account of the IPC/RAS experience in this field. Details on operating conditions, waste and product compositions, decontamination factors, and process equipment are described. The research and development was generally related to the management of intermediate-level radioactive wastes. The waste solutions resulted from recovery and processing of uranium, plutonium, and other products from irradiated nuclear fuel, neutralization of nuclear process solutions after extractant recovery, regeneration of process nitric acid, equipment decontamination, and other radiochemical processes. Waste components include nitric acid, metal nitrate and acetate salts, organic impurities, and surfactants. Waste management operations generally consist of two stages: volume reduction and processing of the concentrates for storage, solidification, and disposal. Filtration, coprecipitation, coagulation, evaporation, and sorption were used to reduce waste volume. 28 figs., 40 tabs

X-ray diffraction of slag-based sodium salt waste forms

Energy Technology Data Exchange (ETDEWEB)

Langton, C. A. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL); Missimer, D. M. [Savannah River Site (SRS), Aiken, SC (United States). Savannah River National Lab. (SRNL)

2014-09-30

The attached report documents sample preparation and x-ray diffraction results for a series of cement and blended cement matrices prepared with either water or a 4.4 M Na salt solution. The objective of the study was to provide initial phase characterization for the Cementitious Barriers Partnership reference case cementitious salt waste form. This information can be used to: 1) generate a base line for the evolution of the waste form as a function of time and conditions, 2) potentially to design new binders based on mineralogy of the binder, 3) understand and predict anion and cation leaching behavior of contaminants of concern, and 4) predict performance of the waste forms for which phase solubility and thermodynamic data are available.

Alternative Electrochemical Salt Waste Forms, Summary of FY11-FY12 Results

Energy Technology Data Exchange (ETDEWEB)

Riley, Brian J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Mccloy, John S. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Crum, Jarrod V. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Lepry, William C. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Rodriguez, Carmen P. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Windisch, Charles F. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Matyas, Josef [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Westman, Matthew P. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Rieck, Bennett T. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Lang, Jesse B. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Olszta, Matthew J. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States); Pierce, David A. [Pacific Northwest National Lab. (PNNL), Richland, WA (United States)

2014-01-17

The Fuel Cycle Research and Development Program, sponsored by the U.S. Department of Energy Office of Nuclear Energy, is currently investigating alternative waste forms for wastes generated from nuclear fuel processing. One such waste results from an electrochemical separations process, called the “Echem” process. The Echem process utilizes a molten KCl-LiCl salt to dissolve the fuel. This process results in a spent salt containing alkali, alkaline earth, lanthanide halides and small quantities of actinide halides, where the primary halide is chloride with a minor iodide fraction. Pacific Northwest National Laboratory (PNNL) is concurrently investigating two candidate waste forms for the Echem spent-salt: high-halide minerals (i.e., sodalite and cancrinite) and tellurite (TeO2)-based glasses. Both of these candidates showed promise in fiscal year (FY) 2009 and FY2010 with a simplified nonradioactive simulant of the Echem waste. Further testing was performed on these waste forms in FY2011 and FY2012 to assess the possibility of their use in a sustainable fuel cycle. This report summarizes the combined results from FY2011 and FY2012 efforts.

Lawrence Livermore National Laboratory Experience Using 30-Gallon Drum Neutron Multiplicity Counter for Measuring Plutonium-Bearing Salts

International Nuclear Information System (INIS)

Dearborn, D M; Keeton, S C

2004-01-01

Lawrence Livermore National Laboratory (LLNL) has been performing accountability measurements of plutonium (Pu) -bearing items with the 30-gallon drum neutron multiplicity counter (NMC) since August 1998. A previous paper focused on the LLNL experience with Pu-bearing oxide and metal items. This paper expands on the LLNL experience with Pu-bearing salts containing low masses of Pu. All Pu-bearing salts used in this study were measured using calorimetry and gamma isotopic analyses (Cal/Iso) as well as the 30-gallon drum NMC. The Cal/Iso values were treated as being the true measure of Pu content because of the inherent high accuracy of the Cal/Iso technique, even at low masses of Pu, when measured over a sufficient period of time. Unfortunately, the long time period required to achieve high accuracy from Cal/Iso can impact other required accountability measurements. The 30-gallon drum NMC is a much quicker system for making accountability measurements of a Pu-bearing salt and might be a desirable tradeoff. The accuracy of 30-gallon drum NMC measurements of Pu-bearing salts, relative to that of Cal/Iso, is presented in relation to the mass range and alpha associated with each item. Conclusions drawn from the use of the 30-gallon drum NMC for accountability measurements of salts are also included

Radioactive waste management and plutonium recovery within the context of the development of nuclear energy in Russia

Energy Technology Data Exchange (ETDEWEB)

Kushnikov, V. [V.G. Khlopin Radium Institute, St. Petersburg (Russian Federation)

1996-05-01

The Russian strategy for radioactive waste and plutonium management is based on the concept of the closed fuel cycle that has been adopted in Russia, and, to a great degree, falls under the jurisdiction of the existing Russian nuclear energy structures. From its very beginning, Russian atomic energy policy was based on finding the most effective method of developing the new fuel direction with the maximum possible utilization of the energy potential from the fission of heavy atoms and the achievement of fuel self-sufficiency through the recycling of secondary fuel. Although there can be no doubt about the importance of economic considerations (for the future), concerns for the safety of the environment are currently of the utmost importance. In this context, spent NPP fuel can be viewed as a waste to be buried only if there is persuasive evidence that such an approach is both economically and environmentally sound. The production of I GW of energy per year is accompanied by the accumulation of up to 800-1000 kg of highly radioactive fission products and approximately 250 kg of plutonium. Currently, spent fuel from the VVER 100 and the RBNK reactors contains approximately 25 tons of plutonium. There is an additional 30 tons of fuel-grade plutonium in the form of purified oxide, separated from spent fuels used in VVER440 reactors and other power production facilities, as well as approximately 100 tons of weapons-grade plutonium from dismantled warheads. The spent fuel accumulates significant amounts of small actinoids - neptunium americium, and curium. Science and technology have not yet found technical solutions for safe and secure burial of non-reprocessed spent fuel with such a broad range of products, which are typically highly radioactive and will continue to pose a threat for hundreds of thousands of years.

Chemical modeling of nuclear waste repositories in the salt repository project

International Nuclear Information System (INIS)

Jansen, G.; Raines, G.E.; Kircher, J.F.; Hubbard, N.

1985-01-01

Salt deposits contain small amounts of water as brine in fluid inclusions in halite and in hydrous minerals, e.g., clays, kieserite (MgSO 4 . H 2 O) and carnallite (KMgCl 3 . 6H 2 O). For the candidate salt deposits, the total amounts of water as volume % brine are: Palo Duro Basin, Texas, approximately 1.8; Paradox Basin, Utah, approximately 5.0 for the carnallite-marker zone, and less than approximately 0.5 below this zone; Gulf Coast salt domes, less than 0.15. For the Palo Duro and Paradox salt, the brines are Mg-rich (approximately 20,000 mg/L to approximately 100,000 mg/L) and sometimes Ca-rich (up to about 20,000 mg/L) NaCl brines. Brine migration calculations have been made using calculations of the time-variant thermal gradient around the waste packages and conservatively high brine volumes in the salt (5.0 volume % for the Texas and Utah sites and 0.5 volume % for the Gulf Coast) as input data. The maximum amounts of brine that eventually migrate to each waste package are about 1.0m 3 (for 5.0 volume % brine) and 0.2m 3 (for 0.5 volume % brine). With current conceptual designs for waste package overpacks (10 to 15 cm thick low-carbon steel), the waste package is not breached by uniform corrosion within 10,000 years. In brines this material thus far shows only uniform corrosion. For the expected conditions, where the brine is provided solely by brine migration, the brine is consumed by reaction with the iron of the overpack nearly as fast as it migrates to the waste package. Therefore, for the expected conditions, data about corrosion rates, radiolysis, etc., are not important. However, it is essential that accurate volumes of in-migrating brine can be calculated

Waste removal sequencing using ProdMod

International Nuclear Information System (INIS)

Paul, P.K.; Gregory, M.V.; Davis, N.R.; Brooke, J.N.

1996-01-01

The Savannah River Site (SRS) is starting to solidify its accumulated high-level radioactive waste into borosilicate glass in stainless steel canisters for eventual permanent storage. The in-tank precipitation process (ITP) and extended sludge processing (ESP) are two key operations in the waste processing complex. The supernate and dissolved salt from the waste storage tanks are transferred to the ITP process tank where the solution is decontaminated in batch processes. Soluble radioactive cesium is precipitated with sodium tetraphenylborate and strontium, uranium, and plutonium are adsorbed on monosodium titanate. The precipitate and adsorbent solids, which now contain the radionuclides, are concentrated using crossflow filters. The concentrated solids are sent to the high-level waste vitrification process. The decontaminated salt solution is sent to the low-level waste solidification process to form cement grout. In parallel with the precipitate operations, insoluble sludges that settled originally to the bottom of the waste tanks are reslurried and sent to ESP to undergo washing to reduce soluble salt content and aluminum dissolution, if required. In the vitrification process in the Defense Waste Processing Facility (DWPF), the concentrated precipitate from the ITP is mixed with the washed sludge from ESP and glass frit in proportion to form a stable borosilicate glass. A novel and fast-running Production Planning Model (ProdMod) has been developed to simulate the waste processing operation. This paper describes the application of ProdMod in sequencing the ITP batches and scheduling the ESP batches

Trial storage of high-level waste in the Asse II salt mine

International Nuclear Information System (INIS)

1984-01-01

This report covers a second phase of the work performed by GSF and KfK in the Asse II salt mine, with a view to disposal of radioactive waste in salt formations. New items of the research were geophysical investigations of the behaviour of heated salt and preparation of a trial storage in the Asse II salt mine

Study on application of molten salt oxidation technology (MSO) for PVC wastes treatment

International Nuclear Information System (INIS)

Tran Thu Ha; Nguyen Hong Quy; Pham Quoc Ky; Nguyen Quang Long; Vuong Thu Bac; Dang Duc Nhan

2007-01-01

The project 'Study on application of molten salt oxidation (MSO) for PVC plastic wastes treatment' aims at three followings: 1) Installation of lab-scale MSO unit with essential compositions builds up foundation for the 2) estimation of waste destruction efficiency of the technology. 3) Based on the results of testing PVC - the chlorinated organic wastes on the lab-scale unit, the ability of the technology application at pilot-scale level will be primary estimated. The adjustment and correction of some compositions in the lab-scale unit theoretically designed during experiment overcame the shortages by design and fabrication such as heat distribution regime, feeding wastes and draining spent salt. These solutions adapt to the technical requirement of operation as well as scientific requirement of the research on MSO process. PVC waste treatment was tested on the MSO lab-scale unit in different conditions of operation temperature, superficial air velocity related to air/oxygen feeding rate, waste feeding rate. The testing results showed that destruction efficiency of chlorine in MSO technology was almost absolute. HCl and Cl 2 emission were insignificant in different operation conditions. HCl and Cl 2 emission depend on resident time and nature of molten salt. However, with inherent attributes of MSO technology emission of CO is not avoided in processing waste treatment. Therefore, finding active solutions for reduction CO emission is essential to complete the technology. The experiments also were carried in conditions of single molten salt (Na 2 CO 3 ) and molten (Na 2 CO 3 - K 2 CO 3 ) eutectic. The comparison of efficiency of these tests gives idea of using molten salt eutectic to reduce operation cost in MSO technology. Based on operation parameters and scientific verification results during experiments, the introductory procedure of waste treatment by MSO process was built up. Thereby, primary estimation of development of the technology in pilot-scale is given

Pyrochemical recovery of plutonium fluoride reduction slag

International Nuclear Information System (INIS)

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

1983-07-01

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

Appraisal of BWR plutonium burners for energy centers

International Nuclear Information System (INIS)

Williamson, H.E.

1976-01-01

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

Waste systems progress report, March 1983 through February 1984

International Nuclear Information System (INIS)

Hickle, G.L.

1984-01-01

Preliminary design engineering for a Beryllum Electrorefining Demonstration Process has been completed and final engineering for fabrication of the process will be completed by the fourth quarter of FY-84. A remotely operated Advanced Size Reduction Facility (ASRF) is under construction and, when completed, will be used for sectioning plutonium-contaminated gloveboxes for disposal. Modification and additions were made to the 82 kg/hr Fluidized Bed Incinerator (FBI) in preparation for turning the unit over to Production. Several types of cementation processes are being developed to treat various TRU and low-level waste streams to reduce the dispersibility of the wastes. Portland cement and Envirostone gypsum cement were investigated as immobilization media for wet precipitation sludges and organic liquid wastes. Transuranic contaminated waste is being retrieved from storage at the Idaho National Engineering Laboratory for examination at Rocky Flats Plant for compliance with the Waste Isolation Pilot Plant-Waste Acceptance Criteria. The removal of unreacted calcium metal from the waste salt formed during the direct oxide reduction of plutonium oxide to plutonium metal is necessary in order to comply with regulations regarding the transportation and storage of waste material containing flammable substances. Chemical methods of denitrification of simulated low-level nitrate wastes were investigated on a laboratory scale. Methods of inserting the carbon composite filters into presently stored and currently generated radioactive waste drums have been investigated and their sealing efficiencies determined. Analyses of carbon tetrachloride (CCl 4 ) recovered from spent lathe coolant revealed contamination levels above usable limits. A handbook covering techniques and processes that have been successfully demonstrated to minimize generation of new transuranic waste is being prepared

Some geotechnical problems related to underground waste disposal in salt formations

International Nuclear Information System (INIS)

Berest, P.

1993-01-01

Nuclear waste disposal in deep salt formations is an option considered by several countries. Rock salt is a very impervious medium, but can be easily leached; selection of an appropriate disposal formation must account for natural protections of the formation as regards water movements. It must be checked that such initially favourable characteristics will not be affected by the existence of shafts and galleries, or by the important heat output generated by vitrified wastes. The discussion is uneasy, for a comprehensive rheological model for rock salt is difficult to set and to be extrapolated to large time scales; some methodological problems are raised by use of numerical computations. (author). 22 refs., 2 figs

The thermo-mechanical behaviour of a salt dome with a heat-generating waste repository

International Nuclear Information System (INIS)

Janssen, L.G.J.; Prij, J.; Kevenaar, J.W.A.M.; Jong, C.J.T.; Klok, J.; Beemsterboer, C.

1984-01-01

This report reviews the analytical work on the disposal of radioactive waste in salt domes performed at ECN in the period 1 January 1980 to 31 December 1982. Chapter 4 in the main report covers the global temperature and deformation analyses of the salt dome and the surrounding rocks. The attached three topical reports cover self-contained parts of the study. The computer program TASTE developed to analyse, at acceptable cost and with, for engineering purposes, sufficient accuracies, the temperature rises in the salt dome due to the stored heat-generating waste is described in Annex 1. Annex 2 gives a description of the extended finite element program GOLIA. The program has been extended to make it suitable for the creep analysis of salt domes with repositories of heat-generating waste. The study on the closing and sealing of boreholes wit heat-generating waste is reported in Annex 3

Electrolytic destruction of oxalate ions in plutonium oxalate supernatant

International Nuclear Information System (INIS)

Michael, K.M.; Talnikar, S.G.; Jambunathan, U.; Kapoor, S.C.; Ramanujam, A.; Venkataraman, N.

1996-01-01

A simple and efficient electrolytic method is described for the destruction of the oxalate ions present in plutonium oxalate supernatant. Using platinum electrode and very little KMnO 4 , in situ generation of Mn 3+ ions is achieved which in turn destroys the oxalate. The use of lower current density helps in achieving maximum current efficiency. The end point is easily detectable by the pink colour of permanganate. By reversing the current, this slight excess of permanganate can be destroyed, thus avoiding the use of hydrogen peroxide. By this simple electrolytic method, the corrosive oxalate ion is completely destroyed and the salt content of the waste solution is considerably reduced. (author). 4 refs., 1 fig., 6 tabs

Backfill barriers for nuclear waste repositories in salt

Energy Technology Data Exchange (ETDEWEB)

Nowak, E J; Odoj, R; Merz, E [eds.

1981-06-01

Backfill materials were evaluated for containment of radionuclides, chemical modification of brine, and sensitivity to hydrothermal conditions. Experimental conditions were relevant to nuclear waste isolation in bedded salt. They were based on geologic conditions at the site of the Waste Isolation Pilot Plant (WIPP) in southeastern New Mexico, USA. Conclusions are: backfill mixtures surrounding the waste form and canister can provide a neutral or slightly acidic, potentially reducing environment, prevent convective aqueous flow, and act as an effective radionuclide migration barrier; bentonite is likely to remain hydrothermally stable but potentially sensitive to waste package interactions which could alter the pH, the ratio of dissolved ions, or the sorption properties of radionuclide species; effects of irradiation from high level waste should be investigated.

A vision for environmentally conscious plutonium processing

International Nuclear Information System (INIS)

Avens, L.R.; Eller, P.G.; Christensen, D.C.; Miller, W.L.

1998-01-01

Regardless of individual technical and political opinions about the uses of plutonium, it is virtually certain that plutonium processing will continue on a significant global scale for many decades for the purposes of national defense, nuclear power and remediation. An unavoidable aspect of plutonium processing is that radioactive contaminated gas, liquid, and solid streams are generated. These streams need to be handled in a manner that is not only in full compliance with today's laws,but also will be considered environmentally and economically responsible now and in the future. In this regard, it is indeed ironic that the multibillion dollar and multidecade radioactive cleanup mortgage that the US Department of Energy (and its Russian counterpart) now owns resulted from waste management practices that were at the time in full legal compliance. The theme of this paper is that recent dramatic advances in actinide science and technology now make it possible to drastically minimize or even eliminate the problematic waste streams of traditional plutonium processing operations. Advanced technology thereby provides the means to avoid passing on to our children and grandchildren significant environmental and economic legacies that traditional processing inevitably produces. This paper will describe such a vision for plutonium processing that could be implemented fully within five years at a facility such as the Los Alamos Plutonium Facility (TA55). As a significant bonus, even on this short time scale, the initial technology investment is handsomely returned in avoided waste management costs

SEPARATION OF URANIUM, PLUTONIUM, AND FISSION PRODUCTS

Science.gov (United States)

Spence, R.; Lister, M.W.

1958-12-16

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

Safe actinide disposition in molten salt reactors

International Nuclear Information System (INIS)

Gat, U.

1997-01-01

Safe molten salt reactors (MSR) can readily accommodate the burning of all fissile actinides. Only minor compromises associated with plutonium are required. The MSRs can dispose safely of actinides and long lived isotopes to result in safer and simpler waste. Disposing of actinides in MSRs does increase the source term of a safety optimized MSR. It is concluded that the burning and transmutation of actinides in MSRs can be done in a safe manner. Development is needed for the processing to handle and separate the actinides. Calculations are needed to establish the neutron economy and the fuel management. 9 refs

An improvement study on the closed chamber distillation system for recovery of renewable salts from salt wastes containing radioactive rare earth compounds

International Nuclear Information System (INIS)

Eun, H.C.; Cho, Y.Z.; Lee, T.K.; Kim, I.T.; Park, G.I.; Lee, H.S.

2013-01-01

In this paper, an improvement study on the closed chamber distillation system for recovery of renewable salts from salt wastes containing radioactive rare earth compounds was performed to determine optimum operating conditions. It was very important to maintain the pressure in the distillation chamber below 10 Torr for a high efficiency (salt recovery >99 %) of the salt distillation. This required increasing the salt vaporization and condensation rates in the distillation system. It was confirmed that vaporization and condensation rates could be improved controlling the given temperature of top of the condensation chamber. In the distillation tests of the salt wastes containing rare earth compounds, the operation time at a given temperature was greatly reduced changing the given temperature of top of the condensation chamber from 780 to 700 deg C. (author)

Rock salt as a medium for long-term isolation of radioactive wastes - a reassessment

International Nuclear Information System (INIS)

Chaturvedi, L.

1985-01-01

Rock salt has been regarded as a suitable medium for the permanent disposal of high and medium level radioactive wastes since the National Academy of Sciences recommended it in 1957. As a result of detained site-specific studies conducted for the Waste Isolation Pilot Plant (WIPP) project in New Mexico, however, several potential problems which are unique to bedded salt deposits have emerged. These include 1) the need to delineate the extent and rate of past dissolution and projections for the future, 2) the origin and significance of brines often found underlying the salt beds, 3) the rate and volume of migration of brine from the salt crystals towards the heat producing waste canisters, 4) the creep rates and implications for retrievability, and 5) the existence of potash and oil and gas resources with implications of human intrusion in the future. These questions will also be faced for sites in salt domes with added complications due to more complex structure and hydrology. The experience at WIPP shows that the site characterization process for high level waste repositories in bedded or dome salt should aim at identifying the important issues of site suitability early in the process and a clear program should be established to address these issues

Salt Repository Project waste emplacement mode decision paper: Revison 1

International Nuclear Information System (INIS)

1987-08-01

This paper provides a recommendation as to the mode of waste emplacement to be used as the current basis for site characterization activity for the Deaf Smith County, Texas, high level nuclear waste repository site. It also presents a plan for implementing the recommendation so as to provide a high level of confidence in the project's success. Since evaluations of high-level waste disposal in geologic repositories began in the 1950s, most studies emplacement in salt formations employed the vertical orientation for emplacing waste packages in boreholes in the floor of the underground facility. This orientation was used in trials at Project Salt Vault in the 1960s. The Waste Isolation Pilot Plant (WIPP) has recently settled on a combination of vertical and horizontal modes for various waste types. This paper analyzes the information available and develops a project position upon which to base current site characterization activities. The position recommended is that the SRP should continue to use the vertical waste emplacement mode as the reference design and to carry the horizontal mode as a ''passive'' alternative. This position was developed based upon the conclusions of a decision analysis, risk assessment, and cost/schedule impact assessment. 52 refs., 6 figs., 1 tab

Sets of Reports and Articles Regarding Cement Wastes Forms Containing Alpha Emitters that are Potentially Useful for Development of Russian Federation Waste Treatment Processes for Solidification of Weapons Plutonium MOX Fuel Fabrication Wastes for

International Nuclear Information System (INIS)

Jardine, L J

2003-01-01

This is a set of nine reports and articles that were kindly provided by Dr. Christine A. Langton from the Savannah River Site (SRS) to L. J. Jardine LLNL in June 2003. The reports discuss cement waste forms and primarily focus on gas generation in cement waste forms from alpha particle decays. However other items such as various cement compositions, cement product performance test results and some cement process parameters are also included. This set of documents was put into this Lawrence Livermore National Laboratory (LLNL) releasable report for the sole purpose to provide a set of documents to Russian technical experts now beginning to study cement waste treatment processes for wastes from an excess weapons plutonium MOX fuel fabrication facility. The intent is to provide these reports for use at a US RF Experts Technical Meeting on: the Management of Wastes from MOX Fuel Fabrication Facilities, in Moscow July 9-11, 2003. The Russian experts should find these reports to be very useful for their technical and economic feasibility studies and the supporting R and D activities required to develop acceptable waste treatment processes for use in Russia as part of the ongoing Joint US RF Plutonium Disposition Activities

PLUTONIUM SOLUBILITY IN HIGH-LEVEL WASTE ALKALI BOROSILICATE GLASS

Energy Technology Data Exchange (ETDEWEB)

Marra, J.; Crawford, C.; Fox, K.; Bibler, N.

2011-01-04

The solubility of plutonium in a Sludge Batch 6 (SB6) reference glass and the effect of incorporation of Pu in the glass on specific glass properties were evaluated. A Pu loading of 1 wt % in glass was studied. Prior to actual plutonium glass testing, surrogate testing (using Hf as a surrogate for Pu) was conducted to evaluate the homogeneity of significant quantities of Hf (Pu) in the glass, determine the most appropriate methods to evaluate homogeneity for Pu glass testing, and to evaluate the impact of Hf loading in the glass on select glass properties. Surrogate testing was conducted using Hf to represent between 0 and 1 wt % Pu in glass on an equivalent molar basis. A Pu loading of 1 wt % in glass translated to {approx}18 kg Pu per Defense Waste Processing Facility (DWPF) canister, or about 10X the current allowed limit per the Waste Acceptance Product Specifications (2500 g/m{sup 3} of glass or about 1700 g/canister) and about 30X the current allowable concentration based on the fissile material concentration limit referenced in the Yucca Mountain Project License Application (897 g/m{sup 3}3 of glass or about 600 g Pu/canister). Based on historical process throughput data, this level was considered to represent a reasonable upper bound for Pu loading based on the ability to provide Pu containing feed to the DWPF. The task elements included evaluating the distribution of Pu in the glass (e.g. homogeneity), evaluating crystallization within the glass, evaluating select glass properties (with surrogates), and evaluating durability using the Product Consistency Test -- Method A (PCT-A). The behavior of Pu in the melter was evaluated using paper studies and corresponding analyses of DWPF melter pour samples.The results of the testing indicated that at 1 wt % Pu in the glass, the Pu was homogeneously distributed and did not result in any formation of plutonium-containing crystalline phases as long as the glass was prepared under 'well-mixed' conditions

Plutonium Solubility In High-Level Waste Alkali Borosilicate Glass

International Nuclear Information System (INIS)

Marra, J.; Crawford, C.; Fox, K.; Bibler, N.

2011-01-01

The solubility of plutonium in a Sludge Batch 6 (SB6) reference glass and the effect of incorporation of Pu in the glass on specific glass properties were evaluated. A Pu loading of 1 wt % in glass was studied. Prior to actual plutonium glass testing, surrogate testing (using Hf as a surrogate for Pu) was conducted to evaluate the homogeneity of significant quantities of Hf (Pu) in the glass, determine the most appropriate methods to evaluate homogeneity for Pu glass testing, and to evaluate the impact of Hf loading in the glass on select glass properties. Surrogate testing was conducted using Hf to represent between 0 and 1 wt % Pu in glass on an equivalent molar basis. A Pu loading of 1 wt % in glass translated to ∼18 kg Pu per Defense Waste Processing Facility (DWPF) canister, or about 10X the current allowed limit per the Waste Acceptance Product Specifications (2500 g/m 3 of glass or about 1700 g/canister) and about 30X the current allowable concentration based on the fissile material concentration limit referenced in the Yucca Mountain Project License Application (897 g/m 3 3 of glass or about 600 g Pu/canister). Based on historical process throughput data, this level was considered to represent a reasonable upper bound for Pu loading based on the ability to provide Pu containing feed to the DWPF. The task elements included evaluating the distribution of Pu in the glass (e.g. homogeneity), evaluating crystallization within the glass, evaluating select glass properties (with surrogates), and evaluating durability using the Product Consistency Test -- Method A (PCT-A). The behavior of Pu in the melter was evaluated using paper studies and corresponding analyses of DWPF melter pour samples.The results of the testing indicated that at 1 wt % Pu in the glass, the Pu was homogeneously distributed and did not result in any formation of plutonium-containing crystalline phases as long as the glass was prepared under 'well-mixed' conditions. The incorporation of 1 wt

Waste form dissolution in bedded salt

International Nuclear Information System (INIS)

Kaufman, A.M.

1980-01-01

A model was devised for waste dissolution in bedded salt, a hydrologically tight medium. For a typical Spent UnReprocessed Fuel (SURF) emplacement, the dissolution rate wll be diffusion limited and will rise to a steady state value after t/sub eq/ approx. = 250 (1+(1-epsilon 0 ) K/sub D//epsilon 0 ) (years) epsilon 0 is the overpack porosity and K/sub d/ is the overpack sorption coefficient. The steady state dissolution rate itself is dominated by the solubility of UO 2 . Steady state rates between 5 x 10 -5 and .5 (g/year) are achievable by SURF emplacements in bedded salt without overpack, and rates between 5 x 10 -7 and 5 x 10 -3 (g/year) with an overpack having porosity of 10 -2

Performance analysis of conceptual waste package designs in salt repositories

International Nuclear Information System (INIS)

Jansen, G. Jr.; Raines, G.E.; Kircher, J.F.

1984-01-01

A performance analysis of commercial high-level waste and spent fuel conceptual package designs in reference repositories in three salt formations was conducted with the WAPPA waste package code. Expected conditions for temperature, stress, brine composition, radiation level, and brine flow rate were used as boundary conditions to compute expected corrosion of a thick-walled overpack of 1025 wrought steel. In all salt formations corrosion by low Mg salt-dissolution brines typical of intrusion scenarios was too slow to cause the package to fail for thousands of years after burial. In high Mg brines judged typical of thermally migrating brines in bedded salt formations, corrosion rates which would otherwise have caused the packages to fail within a few hundred years were limited by brine availability. All of the brine reaching the package was consumed by reaction with the iron in the overpack, thus preventing further corrosion. Uniform brine distribution over the package surface was an important factor in predicting long package lifetimes for the high Mg brines. 14 references, 15 figures

Long-term interactions of full-scale cemented waste simulates with salt brines

Energy Technology Data Exchange (ETDEWEB)

Kienzler, B.; Borkel, C.; Metz, V.; Schlieker, M.

2016-07-01

Since 1967 radioactive wastes have been disposed of in the Asse II salt mine in Northern Germany. A significant part of these wastes originated from the pilot reprocessing plant WAK in Karlsruhe and consisted of cemented NaNO{sub 3} solutions bearing fission products, actinides, as well as process chemicals. With respect to the long-term behavior of these wastes, the licensing authorities requested leaching experiments with full scale samples in relevant salt solutions which were performed since 1979. The experiments aimed at demonstrating the transferability of results obtained with laboratory samples to real waste forms and at the investigation of the effects of the industrial cementation process on the properties of the waste forms. This research program lasted until 2013. The corroding salt solutions were sampled several times and after termination of the experiments, the solid materials were analyzed by various methods. The results presented in this report cover the evolution of the solutions and the chemical and mineralogical characterization of the solids including radionuclides and waste components, and the paragenesis of solid phases (corrosion products). The outcome is compared to the results of model calculations. For safety analysis, conclusions are drawn on radionuclide retention, evolution of the geochemical environment, evolution of the density of solutions, and effects of temperature and porosity of the cement waste simulates on cesium mobilization.

Long-term interactions of full-scale cemented waste simulates with salt brines

International Nuclear Information System (INIS)

Kienzler, B.; Borkel, C.; Metz, V.; Schlieker, M.

2016-01-01

Since 1967 radioactive wastes have been disposed of in the Asse II salt mine in Northern Germany. A significant part of these wastes originated from the pilot reprocessing plant WAK in Karlsruhe and consisted of cemented NaNO 3 solutions bearing fission products, actinides, as well as process chemicals. With respect to the long-term behavior of these wastes, the licensing authorities requested leaching experiments with full scale samples in relevant salt solutions which were performed since 1979. The experiments aimed at demonstrating the transferability of results obtained with laboratory samples to real waste forms and at the investigation of the effects of the industrial cementation process on the properties of the waste forms. This research program lasted until 2013. The corroding salt solutions were sampled several times and after termination of the experiments, the solid materials were analyzed by various methods. The results presented in this report cover the evolution of the solutions and the chemical and mineralogical characterization of the solids including radionuclides and waste components, and the paragenesis of solid phases (corrosion products). The outcome is compared to the results of model calculations. For safety analysis, conclusions are drawn on radionuclide retention, evolution of the geochemical environment, evolution of the density of solutions, and effects of temperature and porosity of the cement waste simulates on cesium mobilization.

Organic tanks safety program FY96 waste aging studies

International Nuclear Information System (INIS)

Camaioni, D.M.; Samuels, W.D.; Linehan, J.C.; Clauss, S.A.; Sharma, A.K.; Wahl, K.L.; Campbell, J.A.

1996-10-01

Uranium and plutonium production at the Hanford Site produced large quantities of radioactive by-products and contaminated process chemicals, which are stored in underground tanks awaiting treatment and disposal. Having been made strongly alkaline and then subjected to successive water evaporation campaigns to increase storage capacity, the wastes now exist in the physical forms of salt cakes, metal oxide sludges, and partially saturated aqueous brine solutions. The tanks that contain organic process chemicals mixed with nitrate/nitrite salt wastes may be at risk for fuel- nitrate combustion accidents. The purpose of the Waste Aging Task is to elucidate how chemical and radiological processes will have aged or degraded the organic compounds stored in the tanks. Ultimately, the task seeks to develop quantitative measures of how aging changes the energetic properties of the wastes. This information will directly support efforts to evaluate the hazard as well as to develop potential control and mitigation strategies

Electrodialysis-based separation process for salt recovery and recycling from waste water

Science.gov (United States)

Tsai, Shih-Perng

1997-01-01

A method for recovering salt from a process stream containing organic contaminants is provided, comprising directing the waste stream to a desalting electrodialysis unit so as to create a concentrated and purified salt permeate and an organic contaminants containing stream, and contacting said concentrated salt permeate to a water-splitting electrodialysis unit so as to convert the salt to its corresponding base and acid.

Immobilization of LiCl-Li 2 O pyroprocessing salt wastes in chlorosodalite using glass-bonded hydrothermal and salt-occlusion methods

Energy Technology Data Exchange (ETDEWEB)

Riley, Brian J.; Peterson, Jacob A.; Kroll, Jared O.; Frank, Steven M.

2018-04-01

In this study, salt occlusion and hydrothermal processes were used to make chlorosodalite through reaction with a high-LiCl salt simulating a waste stream following pyrochemical treatment of oxide-based used nuclear fuel. Some products were reacted with glass binders to increase chlorosodalite yield through alkali ion exchange and aide in densification. Hydrothermal processes included reaction of the salt simulant in an acid digestion vessel with either zeolite 4A or sodium aluminate and colloidal silica. Chlorosodalite yields in the crystalline products were nearly complete in the glass-bonded materials at values of 100 mass% for the salt-occlusion method, up to 99.0 mass% for the hydrothermal synthesis with zeolite 4A, and up to 96 mass% for the hydrothermal synthesis with sodium aluminate and colloidal silica. These results show promise for using chemically stable chlorosodalite to immobilize oxide reduction salt wastes.

Immobilization of LiCl-Li2O pyroprocessing salt wastes in chlorosodalite using glass-bonded hydrothermal and salt-occlusion methods

Science.gov (United States)

Riley, Brian J.; Peterson, Jacob A.; Kroll, Jared O.; Frank, Steven M.

2018-04-01

In this study, hydrothermal and salt-occlusion processes were used to make chlorosodalite through reactions with a high-LiCl salt simulating a waste stream generated from pyrochemical treatment of oxide-based used nuclear fuel. Some products were reacted with glass binders to increase chlorosodalite yield through alkali ion exchange and to aid in densification. Hydrothermal processes included reaction of the salt simulant in an autoclave with either zeolite 4A or sodium aluminate and colloidal silica. Chlorosodalite yields in the crystalline products were nearly complete in the glass-bonded materials at values of 100 mass% for the salt-occlusion method, up to 99.0 mass% for the hydrothermal synthesis with zeolite 4A, and up to 96 mass% for the hydrothermal synthesis with sodium aluminate and colloidal silica. These results show promise for using chemically stable chlorosodalite to immobilize oxide reduction salt wastes.

Waste package materials testing for a salt repository: 1983 status summary report

International Nuclear Information System (INIS)

Moak, D.P.

1986-09-01

The United States plans to safely dispose of nuclear waste in deep, stable geologic formations. As part of these plans, the US Department of Energy is sponsoring research on the designing and testing of waste packages and waste package materials. This fiscal year 1983 status report summarizes recent results of waste package materials testing in a salt environment. The results from these tests will be used by waste package designers and performance assessment experts. Release characteristics data are available on two waste forms (spent fuel and waste-containing glass) that were exposed to leaching tests at various radiation levels, temperatures, pH, glass surface area to solution volume ratios, and brine solutions simulating expected salt repository conditions. Candidate materials tested for corrosion resistance and other properties include iron alloys; TI-CODE 12, the most promising titanium alloy for containment; and nickel alloys. In component interaction testing, synergistic effects have not ruled out any candidate material. 21 refs., 37 figs., 15 tabs

Treatment Study Plan for Nitrate Salt Waste Remediation Revision 1.0

Energy Technology Data Exchange (ETDEWEB)

Juarez, Catherine L. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Funk, David John [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Vigil-Holterman, Luciana R. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Naranjo, Felicia Danielle [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

2016-03-07

The two stabilization treatment methods that are to be examined for their effectiveness in the treatment of both the unremediated and remediated nitrate salt wastes include (1) the addition of zeolite and (2) cementation. Zeolite addition is proposed based on the results of several studies and analyses that specifically examined the effectiveness of this process for deactivating nitrate salts. Cementation is also being assessed because of its prevalence as an immobilization method used for similar wastes at numerous facilities around the DOE complex, including at Los Alamos. The results of this Treatment Study Plan will be used to provide the basis for a Resource Conservation and Recovery Act (RCRA) permit modification request of the LANL Hazardous Waste Facility Permit for approval by the New Mexico Environment Department-Hazardous Waste Bureau (NMED-HWB) of the proposed treatment process and the associated facilities.

Plutonium and americium extraction studies with bifunctional organophosphorus extractants

International Nuclear Information System (INIS)

Navratil, J.D.

1985-01-01

Neutral bifunctional organophosphorus extractants, such as octylphenyl-N,N-diisobutylcarbamoylmethylphosphine oxide (CMPO) and dihexyl-N,N-diethylcarbamoylmethylphosphonate (CMP), are under study at the Rocky Flats Plant (RFP) to remove plutonium and americium from the 7M nitric acid waste. These compounds extract trivalent actinides from strong nitric acid, a property which distinguishes them from monofunctional organiphosphorus reagents. Furthermore, the reagents extract hydroytic plutonium (IV) polymer which is present in the acid waste stream. The compounds extract trivalent actinides with a 3:1 stoichiometry, whereas tetra- and hexavalent actinides extract with a stoichiometry of 2:1. Preliminary studies indicate that the extracted plutonium polymer complex contains one to two molecules of CMP per plutonium ion and the plutonium(IV) maintains a polymeric structure. Recent studies by Horwitz and co-workers conclude that the CMPO and CMP reagents behave as monodentate ligands. At RFP, three techniques are being tested for using CMP and CMPO to remove plutonium and americium from nitric acid waste streams. The different techniques are liquid-liquid extraction, extraction chromatography, and solid-supported liquid membranes. Recent tests of the last two techniques will be briefly described. In all the experiments, CMP was an 84% pure material from Bray Oil Co. and CMPO was 98% pure from M and T Chemicals

Contribution to draft generic environmental impact statement on commercial waste management: radioactive waste isolation in geologic formations

International Nuclear Information System (INIS)

1978-04-01

This document concentrates on deep geologic isolation of wastes in bedded salt, granite, shale, and basalt with emphasis on wastes from three fuel cycles: reprocessing wastes from uranium and plutonium recycling, reprocessing wastes from uranium-only recycling, and spent unreprocessed fuel with no recycling. The analyses presented in this document are based on preconceptual repository designs. As the repository designs progress through future phases, refinements will occur which might modify some of these results. The 12 sections in the report are: introduction; selection and description of generic repository sites; LWR wastes to be isolated in geologic formations; description of waste isolation facilities; effluents from the waste isolation facility; assessment of environment impacts for various geographical locations of a waste isolation facility; environmental monitoring; decommissioning; mine decommissioning site restoration; deep geologic alternative actions; potential mechanisms of containment failure; and considerations relevant to provisional versus final storage

Novel waste printed circuit board recycling process with molten salt

OpenAIRE

Riedewald, Frank; Sousa-Gallagher, Maria

2015-01-01

The objective of the method was to prove the concept of a novel waste PCBs recycling process which uses inert, stable molten salts as the direct heat transfer fluid and, simultaneously, uses this molten salt to separate the metal products in either liquid (solder, zinc, tin, lead, etc.) or solid (copper, gold, steel, palladium, etc.) form at the operating temperatures of 450?470??C. The PCB recovery reactor is essentially a U-shaped reactor with the molten salt providing a continuous fluid, a...

Assessment of tectonic hazards to waste storage in interior-basin salt domes

International Nuclear Information System (INIS)

Kehle, R.

1979-01-01

Salt domes in the northern Gulf of Mexico may make ideal sites for storage of radioactive waste because the area is tectonically quiet. The stability of such salt domes and the tectonic activity are discussed

Plutonium helps probe protein, superconductor

International Nuclear Information System (INIS)

Anon.

1990-01-01

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

Storage of plutonium and nuclear power plant actinide waste in the form of critical-mass-free ceramics containing neutron poisons

Energy Technology Data Exchange (ETDEWEB)

Nadykto, B.A. [RFNC-VNIIEF, Nizhni Novgorod Region (Russian Federation)

2001-07-01

The nuclear weapons production has resulted in accumulation of a large quantity of plutonium and uranium highly enriched with uranium-235 isotope (many tons). The work under ISTC Project 332B-97 treated the issues of safe plutonium storage through making critical-mass-free plutonium oxide compositions with neutron poisons. This completely excludes immediate utilization (without chemical reprocessing) of retained plutonium in nuclear devices. It is therewith possible to locate plutonium most compactly in the storage facility, which would allow reduction in required storage areas and costs. The issues of the surplus weapon-grade plutonium management and utilization have been comprehensively studied in the recent decade. The issues are treated in multiple scientific publications, conferences, and seminars. At the same time, issues of nuclear power engineering actinide waste storage are studied no less extensively. The general issues are material radioactivity and energy release and nuclear accident hazards due to critical mass generation. Plutonium accumulated in nuclear power plant spent fuel is more accessible than weapon-grade plutonium and can become of higher and higher interest with time as its activity reduces, including as material for nuclear devices. The urgency of plutonium management is presently related not only to accumulation of surplus weapon-grade plutonium, but also to the fact that it is high time to decide what has to be done regarding reactor plutonium. Presently, the possibility of actinide separation from NPP spent nuclear fuel and compact underground burial separately from other (mainly fragment) activity is being considered. Actinide and neutron poison base critical-mass-free ceramic materials (similar to plutonium ceramics) may be useful for this burial method. (author)

Storage of plutonium and nuclear power plant actinide waste in the form of critical-mass-free ceramics containing neutron poisons

International Nuclear Information System (INIS)

Nadykto, B.A.

2001-01-01

The nuclear weapons production has resulted in accumulation of a large quantity of plutonium and uranium highly enriched with uranium-235 isotope (many tons). The work under ISTC Project 332B-97 treated the issues of safe plutonium storage through making critical-mass-free plutonium oxide compositions with neutron poisons. This completely excludes immediate utilization (without chemical reprocessing) of retained plutonium in nuclear devices. It is therewith possible to locate plutonium most compactly in the storage facility, which would allow reduction in required storage areas and costs. The issues of the surplus weapon-grade plutonium management and utilization have been comprehensively studied in the recent decade. The issues are treated in multiple scientific publications, conferences, and seminars. At the same time, issues of nuclear power engineering actinide waste storage are studied no less extensively. The general issues are material radioactivity and energy release and nuclear accident hazards due to critical mass generation. Plutonium accumulated in nuclear power plant spent fuel is more accessible than weapon-grade plutonium and can become of higher and higher interest with time as its activity reduces, including as material for nuclear devices. The urgency of plutonium management is presently related not only to accumulation of surplus weapon-grade plutonium, but also to the fact that it is high time to decide what has to be done regarding reactor plutonium. Presently, the possibility of actinide separation from NPP spent nuclear fuel and compact underground burial separately from other (mainly fragment) activity is being considered. Actinide and neutron poison base critical-mass-free ceramic materials (similar to plutonium ceramics) may be useful for this burial method. (author)

Low disposal of radioactive wastes in salt formations of the Federal Republic of Germaany

International Nuclear Information System (INIS)

Albrecht, E.

1980-01-01

The salt formations of northern Europe are generally suitable for the storage of radioactive wastes because the region is largely free from earthquakes and the salt formations known as diapires provide effective hydrological sealing. The Federal Republic of Germany employed the Asse Salt Mine of Lower Saxony for research in waste storage. More recently, exploratory work has begun on the construction of a large recycling and disposal plant at the Gorleben salt dome. The geology, hydrology, rock mechanics, and seismicity of the two sites are briefly discussed, including a discussion of experiences gained so far from the Asse site. 11 refs

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

International Nuclear Information System (INIS)

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

1989-01-01

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

Removal of salt from high-level waste tanks by density-driven circulation or mechanical agitation

International Nuclear Information System (INIS)

Kiser, D.L.

1981-01-01

Twenty-two high-level waste storage tanks at the Savannah River Plant are to be retired in the tank replacement/waste transfer program. The salt-removal portion of this program requires dissolution of about 19 million liters of salt cake. Steam circulation jets were originally proposed to dissolve the salt cake. However, the jets heated the waste tank to 80 to 90 0 C. This high temperature required a long cooldown period before transfer of the supernate by jet, and increased the risk of stress-corrosion cracking in these older tanks. A bench-scale investigation at the Savannah River Laboratory developed two alternatives to steam-jet circulation. One technique was density-driven circulation, which in bench tests dissolved salt at the same rate as a simulated steam circulation jet but at a lower temperature. The other technique was mechanical agitation, which dissolved the salt cake faster and required less fresh water than either density-driven circulation or the simulated steam circulation jet. Tests in an actual waste tank verified bench-scale results and demonstrated the superiority of mechanical agitation

Decommissioning and Decontamination Program: Battelle Plutonium Facility, Environmental assessment

International Nuclear Information System (INIS)

1979-09-01

This assessment describes the decontamination of Battelle-Columbus Plutonium Facility and removal from the site of all material contamination which was associated with or produced by the Plutonium Facility. Useable uncontaminated material will be disposed of by procedures normally employed in scrap declaration and transfer. Contaminated waste will be transported to approved radioactive waste storage sites. 5 refs., 1 fig

Safe disposal of surplus plutonium

Science.gov (United States)

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

2001-06-01

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

Molt salts reactors capacity for wastes incineration and energy production

International Nuclear Information System (INIS)

David, S.; Nuttin, A.

2005-01-01

The molten salt reactors present many advantages in the framework of the IV generation systems development for the energy production and/or the wastes incineration. After a recall of the main studies realized on the molten salt reactors, this document presents the new concepts and the identified research axis: the MSRE project and experience, the incinerators concepts, the thorium cycle. (A.L.B.)

Considerations of the Differences between Bedded and Domal Salt Pertaining to Disposal of Heat-Generating Nuclear Waste

Energy Technology Data Exchange (ETDEWEB)

Hansen, Francis D. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Kuhlman, Kristopher L. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Sobolik, Steven R. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

2016-07-07

Salt formations hold promise for eternal removal of nuclear waste from our biosphere. Germany and the United States have ample salt formations for this purpose, ranging from flat-bedded formations to geologically mature dome structures. As both nations revisit nuclear waste disposal options, the choice between bedded, domal, or intermediate pillow formations is once again a contemporary issue. For decades, favorable attributes of salt as a disposal medium have been extoled and evaluated, carefully and thoroughly. Yet, a sense of discovery continues as science and engineering interrogate naturally heterogeneous systems. Salt formations are impermeable to fluids. Excavation-induced fractures heal as seal systems are placed or natural closure progresses toward equilibrium. Engineering required for nuclear waste disposal gains from mining and storage industries, as humans have been mining salt for millennia. This great intellectual warehouse has been honed and distilled, but not perfected, for all nuances of nuclear waste disposal. Nonetheless, nations are able and have already produced suitable license applications for radioactive waste disposal in salt. A remaining conundrum is site location. Salt formations provide isolation and geotechnical barriers reestablish impermeability after waste is placed in the geology. Between excavation and closure, physical, mechanical, thermal, chemical, and hydrological processes ensue. Positive attributes for isolation in salt have many commonalities independent of the geologic setting. In some cases, specific details of the environment will affect the disposal concept and thereby define interaction of features, events and processes, while simultaneously influencing scenario development. Here we identify and discuss high-level differences and similarities of bedded and domal salt formations. Positive geologic and engineering attributes for disposal purposes are more common among salt formations than are significant differences