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Sample records for finales du plutonium

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

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

    1968-07-01

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

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

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

    1959-07-01

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

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

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

    1967-07-01

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

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

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

    1955-07-01

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

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

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

    1967-07-01

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

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

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

    1967-07-01

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

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

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

    1967-09-15

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

  8. 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)

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

    1962-07-01

    facteurs physiques sur la vitesse de fluoration du tetrafluorure de plutonium solide par le fluor. Dans un appareil a four horizontal et circulation de fluor a la pression atmospherique de 520 deg. C, avec un debit de fluor pur de 9 l.h{sup -1}, il est possible de transformer une charge de 3 g de tetrafluorure en hexafluorure avec un taux de transformation d'environ 100 pour cent et un rendement de recuperation superieur a 90 pour cent, en 4 a 5 h. La vitesse de fluoration est fonction de la temperature du debit de fluor, de la surface de la nacelle, de l'epaisseur de la couche de tetrafluorure et du temps de reaction. Elle ne depend pas de la diffusion du fluor dans le Solide mais est commandee par la reaction a l'interface gaz-solide et suit la loi cinetique (1 - T{sub T}){sup 1/3} = kt + 1. L'existence de fluorures intermediaires, en particulier Pu{sub 4} F{sub 17}, est confirmee par une cassure de la droite d'Arrhenius vers 370 deg. C, par des differences dans les vitesses de fluoration au sein de la couche de tetrafluorure et par des variations reversibles de coloration. La transformation en hexafluorure s'accompagne d'une purification vis-a-vis des elements etrangers entrant dans la composition de plutonium initial. Recuperation du plutonium des scories d'elaboration: L'etude est basee sur la transformation en hexafluorure gazeux des grains de plutonium occlus dans les scories d'elaboration, cet hexafluorure devant fournir par decomposition thermique un tetrafluorure directement recyclable au stade elaboration. - Dans les conditions envisagees, ce procede n'est pas utilisable industriellement. Apres broyage, une Reparation par milieu dense (iodure de methylene) permet de separer une scorie enrichie en plutonium (75 pour cent du Pu dans 2,6 pour cent du poids des scories) et une scorie pauvre. Par fluoration prolongee (16 h) des diverses portions recueillies, il est possible de recuperer environ 80 pour cent du plutonium. Un appareillage de traitement base sur la

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

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

    1960-07-01

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

  10. A rapid method of dosing plutonium in radioactive effluents; Methode de dosage rapide du plutonium dans les effluents radioactifs (1961)

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    Scheidhauer, J; Messainguiral, L [Commissariat a l' Energie Atomique, Centre de Production de Plutonium, Marcoule (France). Centre d' Etudes Nucleaires

    1961-07-01

    The plutonium is first separated by a lanthanum fluoride precipitation. The precipitated fluorides are dissolved in normal nitric acid solution in the presence of aluminium nitrate. The plutonium transformed to the tetravalent state is then extracted with thenoyltrifluoroacetone and returned to the aqueous phase with 10 N nitric acid. After evaporation on a watch glass the residue is calcined on a Meker burner and counted using a counting system fitted with a zinc sulphide scintillator. When necessary, the calcium is eliminated at the beginning of the dosage by a fluoride precipitation, the plutonium being oxidised to the valency IV. (authors) [French] Le plutonium est d'abord separe par entrainement au fluorure de lanthane. Le precipite des fluorures est remis en solution en milieu acide nitrique normal, en presence de nitrate d'aluminium. Le plutonium amene a la valence IV est alors extrait par la thenoyltrifluoroacetone et remis en phase aqueuse dans l'acide nitrique 10 N. Apres evaporation sur verre de montre, le residu est calcine sur bec Meker et compte sur un ensemble de comptage equipe d'un scintillateur au sulfure de zinc. Lorsque cela est necessaire, le calcium est elimine, au debut du dosage, par precipitation du fluorure, le plutonium etant oxyde a la valence VI. (auteurs)

  11. Dosage of plutonium by isotopic dilution in irradiated fuels; Dosage du plutonium par dilution isotopique dans les combustibles irradies

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

    1964-07-01

    Plutonium determination in irradiated fuels has been carried out for several years by isotopic dilution by Sebaci and SSM in collaboration. SECACI has made available to the SSM the necessary space and equipment in its Fontenay laboratories. This work has shown the importance of the valency cycle which should make it possible to obtain a uniform isotopic distribution in sample tracer mixtures, and also a satisfactory U/Pu separation. Now it has been noticed that the presence of an excess of uranium considerably modifies the oxidation-reduction reaction kinetics of the plutonium. We have therefore been led to change certain parts of the operational technique so as to have an efficient cycle and to thereby improve the U/Pu separation; the stability of the thermionic emission of the plutonium, connected to the quantity of residual uranium, has at the same time been improved and we can now carry out more precise isotopic analyses. We have also tried to eliminate as far as possible the isotopic contaminations by:using a more rational operational method; the equipment used has been the object of a special study. The evaporations are carried out so as to prevent the formation of saturated vapours inside the glove box. The material which cannot be changed after each operation is carefully cleaned every time a new sample is treated. With this technique, a second calibration of the tracer T{sub 2} has been undertaken using a new standard solution. This solution has been prepared very carefully by weighing uranium and plutonium of known chemical purity, and we believe that it can be guaranteed to be a good reference solution. The value of the {sup 233}U/{sup 242}Pu ratio of the tracer has been obtained with a relative accuracy of 0,5 per cent. This modified method is now being applied to the analysis of rods irradiated in G-3. (author) [French] La determination du plutonium par dilution isotopique dans les combustibles irradies est pratiquee depuis plusieurs annees en

  12. Purification and final concentration of the plutonium obtained by treatment of irradiated uranium at the Fontenay-aux-Roses pilot plant; Purification et concentration finales du plutonium en fin de traitement de l'uranium irradie a l'usine-pilote de Fontenay-aux-Roses

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

    1958-07-01

    This paper consists of: 1- a recapitulation of the laboratory tests which led to the choice of the method; 2- a description of the latter, with the results obtained at the Fontenay-aux-Roses pilot plant; 3- the analytical methods used for checking and verifying the purity of the plutonium. (author)Fren. [French] Cet expose comprend: 1- le rappel des essais de laboratoire qui ont conduit au choix du procede; 2- la description de ce dernier, avec les resultats obtenus a l'Usine-Pilote de Fontenay-aux-Roses; 3- les methodes analytiques utilisees pour le controle et pour la verification de la purete du plutonium. (auteur)

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

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

    1968-07-01

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

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

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

    1963-07-01

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

  15. Plutonium separation and the measurement of its concentration in natural waters (1963); Separation du plutonium et mesure de sa concentration dans les eaux naturelles

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    Scheidhauer, J; Messainguiral, L; Meiraneisio, A M [Commissariat a l' Energie Atomique, Centre de Production de Plutonium, Marcoule (France). Centre d' Etudes Nucleaires

    1963-07-01

    After concentration by chemisorption on a calcium fluoride suspension, the plutonium is purified and isolated by xylene extraction of the complex formed with T.T.A. The radioelement is measured by counting with a ZnS (Ag) scintillator after evaporation or electrolysis. (authors) [French] Apres concentration par chimisorption sur une suspension de fluorure de calcium, le plutonium est purifie et isole par extraction au xylene du complexe forme avec la T.T.A. La mesure du radioelement est effectuee par comptage au scintillateur S Zn (Ag) apres evaporation ou electrolyse. (auteurs)

  16. Measurement and regulation of the level of a homogeneous plutonium reactor; Mesure et regulation du niveau d'un reacteur homogene au plutonium

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    Berger, F; Bertrand, J

    1958-12-01

    Reactivity depends strongly on disturbances of the level of the plutonium solution In the homogeneous reactor. Proserpine has a small cylindrical core, 250 mm diameter, and 10 liters volume. With a view to reducing the dangers due to corrosion and contamination, the solution level in the core is raised by pneumatic pressure. The level is stabilized by means of a regulating system. During critical experiments the variations of the level are less than one hundredth part of a millimeter. (author) [French] Les variations du niveau de la solution de plutonium dans le reacteur homogene Proserpine ont une grosse influence sur la reactivite, car le coeur est petit (10 litres de solution dans un cylindre de diametre 250 mm). En vue de reduire les dangers dus a la corrosion et a la contamination, la commande du volume liquide est pneumatique. Nous avons realise la stabilite du niveau par une regulation qui, dans les essais en regime critique, limite les variations du plan liquide a une fraction de centieme de millimetre. (auteur)

  17. New measurements in plutonium L X ray emission spectrum using an electron probe micro-analyser; Nouvelles mesures dans le spectre d'emission L du plutonium au moyen d'un micro analyseur a sonde electronique

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    Bobin, J L; Despres, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1966-07-01

    Further studies by means of an electron-probe micro-analyser, allowed report CEA-R--1798 authors to set up a larger plutonium X ray spectrum table. Measurements of plutonium L{sub II} and L{sub III} levels excitation potentials have also been achieved. Some remarks about apparatus performance data (such as spectrograph sensibility, resolving power and accuracy) will be found in the appendix. (authors) [French] Poursuivant les etudes exposees dans le rapport CEA-R--1798, les auteurs ont pu dresser un tableau plus etendu du spectre L du plutonium, au moyen du micro-analyseur a sonde electronique. Ils ont egalement effectue des mesures de potentiel d'excitation des niveaux L{sub II} et L{sub III} du plutonium. On trouvera en annexe quelques notes sur les constantes d'appareillage (sensibilite, pouvoir de resolution et precision des spectrographes). (auteurs)

  18. X-spectrographic method for plutonium detection. Application to contamination measurements in humans; Etude d'une methode de detection du plutonium par spectrographie X. Application a la mesure des contaminations sur l'homme

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

    1967-07-01

    After reviewing the radio-toxicology of plutonium 239 and conventional detection methods using its {alpha}-radiation, the author considers the measurement of the X emission spectrum of plutonium 239 using a proportional counter filled with argon under pressure. This preliminary work leads to the third part of this research involving the detailed study of the possibilities of applying thin alkali halide crystal scintillators to the detection of soft plutonium X-rays; there follows a systematic study of all the parameters liable to render the detection as sensitive as possible: movement due to the photomultiplier itself and its accessory electronic equipment, nature and size of the crystal scintillator as well as its mode of preparation, shielding against external parasitic radiation. Examples of some applications to the measurement of contamination in humans give an idea of the sensitivity of this method. (author) [French] Apres un apercu de la radiotoxicologie du plutonium 239 et des methodes classiques de detection par son rayonnement {alpha}, on etudie le spectre d'emission X du plutonium 239 avec un compteur proportionnel rempli avec de l'argon sous pression. Ce travail preliminaire permet d'aborder la troisieme partie de cette etude dans laquelle nous examinons d'une fagon approfondie les possibilites d'application des cristaux scintillateurs minces d'halogenure alcalin a la detection du rayonnement X mou du plutonium; suit une etude systematique de tous les parametres susceptibles de rendre la detection aussi sensible que possible: mouvement propre du photomultiplicateur et de l'electronique associee, nature et dimensions du cristal scintillateur ainsi que son mode de fabrication, blindage contre les rayonnements parasites exterieurs. Quelques applications a la mesure des contaminations sur l'homme permettent d'apprecier la sensibilite de cette methode. (auteur)

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1958-07-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1961-11-15

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1958-07-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1998-06-29

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

  3. Economic Effect on the Plutonium Cycle of Employing {sup 235}U in Fast Reactor Start-Up; Incidence Economique du Demarrage des Reacteurs Rapides a l'Aide d'Uranium-235 sur le Cycle du Plutonium

    Energy Technology Data Exchange (ETDEWEB)

    Van Dievoet, J.; Egleme, M.; Hermans, L. [BELGONUCLEAIRE, Bruxelles (Belgium)

    1967-09-15

    factors, inventory factors) from one cycle to another, with a comparative study of the use of {sup 235}U in thermal and fast reactors, variations in the discounted fuel cycle costs from one cycle to another, and weight and characteristics of the recycled fuel, of the additional fuel required and of excess fuel. (author) [French] Le memoire presente les premiers resultats d'une etude entreprise dans le cadre d'un contrat d'association Euratom-Belgique et destinee a evaluer l'interet de l'alimentation de reacteurs rapides en uranium-235. Plusieurs possibilites se presentent pour le demarrage d'un reacteur rapide a l'aide d'uranium-235. 1. Le reacteur peut etre alimente en permanence avec de l'uranium enrichi, le plutonium produit servant a demarrer et a alimenter d'autres reacteurs; dans ce cas, l'uranium est recycle dans le reacteur en y ajoutant de l'uranium enrichi. 2. Le plutonium produit dans le reacteur peut etre partiellement recycle dans celui-ci, ainsi que l'uranium; dans ce cas, le reacteur se transforme progressivement en un reacteur au plutonium. Ces deux cas peuvent etre combines pour un reacteur a plusieurs zones d'enrichissement, ou l'on peut appliquer simultanement les deux politiques a des zones differentes, c'est-a-dire: alimenter, par exemple, la zone interne en uranium enrichi et recycler le plutonium dans la zone externe. Le mode de traitement du combustible irradie rend egalement le probleme complexe, selon que l'on traite ensemble ou separement le coeur et les couvertures axiales; de meme, pour un reacteur a plusieurs zones d'enrichissement, celles-ci peuvent etre traitees ensemble ou separement. Les calculs sont effectues a l'aide d'un code de calcul utilisant, pour lavpartie relative aux caracteristiques des reacteurs successifs, les coefficients d'equivalence definis par Baker and Ross et, pour la partie economique, la methode du cout actualise du cycle du combustible. Dans la premiere phase des travaux, une analyse approcheedu phenomene a ete

  4. Study of allotropic transformations in plutonium; Etude des transformations allotropiques du plutonium

    Energy Technology Data Exchange (ETDEWEB)

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

    1966-06-01

    The allotropic transformations in plutonium have been studied by different methods: metallography, dilatometry, thermal analysis, resistivity measurements, examination with a hot stage microscope. In order to study the importance of the purity, purification process such as zone-melting or electro-diffusion have been developed. The characteristics of the {alpha} {r_reversible} {beta} transformation can be explained in terms of the influence of internal stresses on the transition temperature and on the transformation kinetics. Some particular characteristics of {delta} {yields} {gamma}, {gamma} {yields} {alpha}, {delta} {r_reversible} {epsilon}, {beta} {r_reversible} {gamma} and {delta} {yields} {alpha} transformations are also given. (author) [French] Les transformations, allotropiques du plutonium ont ete etudiees a l'aide de differentes methodes: metallographie, dilatometrie, analyse thermique, mesure de resistivite, examen au microscope a platine chauffante. Pour preciser l'influence de la purete, des procedes de purification comme la fusion de zone ou l'electrodiffusion ont ete mis au point. Les caracteres de la transformation {alpha} {r_reversible} {beta} s'expliquent par le role des contraintes internes sur la temperature de transition et la cinetique de transformation. Quelques particularites des transformations {delta} {yields} {gamma}, {gamma} {yields} {alpha}, {delta} {r_reversible} {epsilon}, {beta} {r_reversible} {gamma} et {delta} {yields} {alpha} sont egalement presentees. (auteur)

  5. Plutonium in depleted uranium penetrators

    International Nuclear Information System (INIS)

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

    2002-01-01

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

  6. Radiochemical Determination of Plutonium for Radiological Purposes; Determination Radiochimique du Plutonium a des Fins Radiologiques; Radiokhimicheskoe opredelenie plutoniya dlya tselej radiologii; Determinacion Radioquimica del Plutonio con Fines Radiologicos

    Energy Technology Data Exchange (ETDEWEB)

    Nielsen, J. M.; Beasley, T. M. [Chemical Laboratory, Hanford Laboratories, General Electric Company, Richland, WA (United States)

    1964-10-15

    In this paper the procedures that have been and are currently being used for the determination of micro- microgram quantities of plutonium in biological and environmental samples are reviewed. Special emphasis is placed on excretion analysis. Expected urinary excretion rates have been calculated, using assumed levels of plutonium deposition, so that the analytical sensitivities of various procedures can be compared. Complete dissolution of excreta, soil, bone, tissue and vegetation are described with emphasis on avoiding the formation of refractory compounds of plutonium which are soluble with difficulty. Analytical methods for plutonium analysis of these materials are reviewed and include co-precipitation, liquid-liquid extraction, ion exchange chromatography and the use of plutonium isotopes for yield determinations by means of alpha energy analysis. Using counting statistics, comparisons are made of the sensitivities available in low-level alpha counting, using ionization chambers,- proportional counters, diode counters, and nuclear track emulsions. Isotopic analysis of plutonium by alpha spectrometry, nuclear emulsion techniques, and liquid scintillation counting are included. The use of non-isotopic carriers as a source of extraneous activity and the environmental levels of plutonium recently encountered around the world are discussed in connection with ''blank'' samples. Two possibilities are considered for future methods of plutonium analysis where increased sensitivity is required. These are activation analysis and fission fragment counting. (author) [French] Les auteurs examinent l'ensemble des methodes que l'on a employees et que Ton emploie actuellement pour evaluer les quantites de plutonium de l'ordre du picogramme presentes dans des echantillons biologiques et mesologiques. Ils insistent particulierement sur l'analyse des excreta. Ils ont calcule des taux d'elimination urinaire probables a partir de concentrations de plutonium theoriques, de maniere a

  7. Study of the long-term values and prices of plutonium; a simplified parametrized model; Etude des valeurs et des prix du plutonium a long terme; un modele parametre simplifie

    Energy Technology Data Exchange (ETDEWEB)

    Gaussens, J; Paillot, H [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1965-07-01

    The authors define the notions of use values and price of plutonium. They give a 'simplified parametrized model' simulating the equilibrium of the offer and the demand in time, concerning the plutonium and the price deriving from the relative scarcity of this metal, taking into account the technical and economic operating parameters of the various reactors confronted. This model is simple enough to allow direct computations and establish clear relations between the various parameters. The use of the linear programmes method allows on the other hand a wide extension of the model. This report includes three main parts: I - General description of the study (without detailed calculations) II - Mathematical development of the simplified parametrized model and application (the basic data and the results of the calculations are given) III - Appendices (giving the detailed computations of part II). (authors) [French] Les auteurs definissent les notions de valeurs d'usage et de prix du plutonium. Ils donnent un 'modele parametre simplifie' simulant l'equilibre de l'office et de la demande dans le temps concernant le plutonium et le prix qui decoule de la rarete relative de ce metal, compte tenu des parametres techniques et economiques de fonctionnement des divers reacteurs en presence. Ce modele est suffisamment simple pour permettre des calculs manuels et etablir des liaisons claires entre les divers parametres. L'utilisation de la technique des programmes lineaires permet par ailleurs une extension considerable du modele. Cette note comprend trois parties: I - Expose general de l'etude (sans expose du detail des calculs) II - Developpement mathematique du modele parametre simplifie et application (on precise les donnees de base et le resultat des calculs) III - Annexes (donnant le detail des calculs de la partie II). (auteurs)

  8. Analytical methods used in plutonium purification cycles by trilaurylamine; Methodes analytiques utilisees dans les cycles de purification du plutonium par la trilaurylamine

    Energy Technology Data Exchange (ETDEWEB)

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

    1965-07-01

    The utilisation of trilaurylamine as a solvent extractant for the purification of plutonium has entailed to perfect a set of analytical methods which involves, various techniques. The organic impurities of the solvent can be titrated by gas-liquid chromatography. The titration of the main degradation product, the di-laurylamine, can be accomplished also by spectro-colorimetry. Potentiometry is used for the analysis of the different salts of amine-nitrate-sulfate-bisulfate as also the extracted nitric acid. The determination of the nitrate in aqueous phase is carried out by constant current potentiometry. The range of application, the accuracy and the procedure of these analysis are related in the present report. (author) [French] L'utilisation de la trilaurylamine comme solvant d'extraction pour la purification du plutonium a necessite la mise au point d'un ensemble de methodes analytiques qui ressortent de techniques diverses. Les impuretes organiques du solvant peuvent etre dosees par chromatographie gaz-liquide. Le dosage du principal produit de degradation, la dilaurylamine, peut egalement etre effectue par spectrocolorimetrie. La potentiometrie est utilisee pour les analyses des differents sels d'amine: nitrate, sulfate, bisulfate, ainsi que de l'acide nitrique extrait. La determination des nitrates en phase aqueuse est executee par potentiometrie a courant impose. Le domaine d'application, la precision et le mode operatoire de ces analyses sont indiques dans le present rapport. (auteur)

  9. Technical note concerning the use of cellulose ester filtering membranes in the determination of plutonium in urine; Note technique sur l'utilisation des membranes filtrantes d'esters de cellulose dans le dosage du plutonium dans les urines

    Energy Technology Data Exchange (ETDEWEB)

    Harduin, J C; Montels, P [Commissariat a l' Energie Atomique, la Hague (France)

    1968-07-01

    During the last stage of the determination of plutonium in biological media, cellulose ester filtering membranes are used for collecting, with the help of a special device, the very fine precipitate resulting from the co-precipitation of plutonium and lanthanum fluorides. The membranes are then dried, and stuck on to flat watch-glasses for a {alpha} counting. A method is then given for purifying the lanthanum so as to keep the background noise during counting as low as possible. (author) [French] Dans la phase terminale du dosage du plutonium dans les milieux biologiques, on utilise les membranes filtrantes d'esters de cellulose pour recueillir, a l'aide d'un dispositif particulier, le precipite tres tenu resultant de la co-precipitation plutonium-lanthane sous forme de fluorure - Les membranes sont ensuite sechees puis collees sur verre de montre plat avant d'etre passees au compteur alpha. Un mode de purification du lanthane est ensuite donne afin de ne pas augmenter le bruit de fond des appareils de comptage. (auteur)

  10. Kinetic study of the fluorination by fluorine of some uranium and plutonium compounds; Etude cinetique de la fluoration par le fluor de quelques composes de l'uranium et du plutonium

    Energy Technology Data Exchange (ETDEWEB)

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

    1964-12-15

    The study of fluorination reactions of uranium and plutonium compounds with elementary fluorine, has been carried out using a thermogravimetric method. These reactions are heterogeneous ones, and of the following type: S(solid) + G{sub 1}(gas) - G{sub 2}(gas). The kinetics of these reactions correspond to a uniform attack of the entire surface of the sample. {alpha}: being the degree of completion of the reaction, k(rel): being the relative rate of penetration of the reaction interface, t: being the time, one have the relation: (1-{alpha}){sup 1/3} = 1 - k(rel)*t. The mechanism of the reaction varies according to the nature of the compound: 1) with uranium tetrafluoride and plutonium tetrafluoride, the reaction proceeds in a single step; 2) with uranium oxides, the reaction proceeds in two steps, uranium oxyfluoride being the intermediate compound; 3) with plutonium oxide, the reaction proceeds in two steps, plutonium tetrafluoride being the intermediate compound; and 4) with uranium trichloride, the mechanism is complex: chlorine trifluoride is formed. (author) [French] L'etude des reactions de fluoration par le fluor, de composes de l'uranium et du plutonium a ete faite par thermogravimetrie. Ce sont des reactions heterogenes du type: S(solide) + G{sub 1}(gaz) - G{sub 2}(gaz). La cinetique de ces reactions est celle correspondant a une attaque uniforme de toute la surface de l'echantillon. Si {alpha}: est le degre d'avancement de la reaction, k(rel): est la vitesse relative d'avancement d'un interface reactionnel, t: le temps. On a la relation: (1-{alpha}){sup 1/3} = 1-k(rel)*t. Le mecanisme de la reaction varie selon la nature du compose: 1) tetrafluorure d'uranium et tetrafluorure de plutonium, la reaction s'effectue en un seul stade; 2) Oxydes d'uranium: la reaction s'effectue en deux stades, l'oxyfluorure d'uranium est le compose intermediaire; 3) oxyde de plutonium, la reaction s'effectue en deux stades, la tetrafluorure de plutonium est le compose

  11. Observation of allotropic transformations of plutonium with a hot stage microscope; Etude des transformations allotropiques du plutonium au microscopic a platine chauffante

    Energy Technology Data Exchange (ETDEWEB)

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

    1965-07-01

    A hot stage microscope designed for the examination of plutonium and its alloys is described. This apparatus was used to study the {alpha} {r_reversible} {beta} and {delta} {r_reversible} {epsilon} allotropic transformations of pure or {beta} and {delta} stabilised plutonium. The {alpha} {yields} {beta} transformation is typically a nucleation and growth process. Some particularities caused by the internal stresses due to the volume change during this transformation are examined. The kinetics has been studied as a function of these stresses and a temperature dependent activation energy for nucleation has been deduced. The {beta} {yields} {alpha} transformation presents a memory effect which implies an orientation relationship between the two phases. This fact is probably caused by the stresses created during the {beta} {yields} {alpha} transition. The {beta} {r_reversible} {gamma} and {delta} {r_reversible} {epsilon} transformations are also diffusion governed processes. (authors) [French] On decrit un microscope a platine chauffante permettant l'examen du plutonium et de ses alliages. Cet appareil a servi a l'etude des transformations {alpha} {r_reversible} {gamma} et {delta} {r_reversible} {epsilon} du plutonium pur ou stabilise en phase {beta} et {delta}. La transformation {alpha} {yields} {beta} est une transformation typique par germination et croissance; elle presente des caracteristiques bien particulieres qui sont dues aux contraintes internes qui prennent naissance au changement de volume a la transformation; la cinetique a ete etudiee en fonction de ces contraintes, et on en a deduit une energie d'activation pour la germination variable avec la temperature. La transformation {beta} {yields} {alpha} presente un effet de memoire qui suppose une relation d'orientation entre les deux phases; ce phenomene semble lie comme auparavant aux contraintes creees par le passage {beta} {yields} {alpha}. Les transformations {beta} {r_reversible} {gamma} et {delta} {r

  12. Detection of {alpha} particles using semiconductors. Application to the control of plutonium extraction; Detection des particules {alpha} par semiconducteurs application au controle de l'extraction du plutonium

    Energy Technology Data Exchange (ETDEWEB)

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

    1968-03-01

    A study is made of a particles produced by thick sources, using either diffused junction or surface barrier semiconductor detectors for controlling continuously the plutonium extraction process. For this, a presenting apparatus is described in which the solutions to be analyzed flow in contact with the detector protected by a thin mica membrane. A method is described which gives a precise recording of the spectra and which thus allows the separation of two or more {alpha} emitters present in the same solution. This method has been applied to the measurement of {sup 239}Pu in the the presence of {sup 241}Am with an accuracy of {+-}5 per cent. In the second part of the report is considered the detection of plutonium in solutions of {beta} - {gamma} emitting fission products. Pile-up is reduced by using a fast amplification chain associated to totally depleted thin detectors. Under these conditions a few mg of {sup 239}Pu can be detected in solutions of fission products having an activity of 100 curies/liter. A method is given for discriminating {alpha} and {beta} particles, it is based on the difference in the collection times for the charges liberated by these particles in the detector. (author) [French] On etudie la detection de particules {alpha} issues de sources epaisses par detecteurs semiconducteurs a jonction diffusee ou a barriere de surface pour le controle continu du procede d'extraction du plutonium. A cet effet on decrit un appareil presentateur dans lequel les solutions a analyser circulent au contact du detecteur protege par une membrane mince de mica. On decrit une methode qui permet par le trace precis des spectres de separer deux ou plusieurs emetteurs {alpha} presents dans une meme solution. Cette methode a ete appliquee a la mesure du {sup 239}Pu en presence de {sup 241}Am avec une precision de {+-} 5 pour cent. Dans la deuxieme partie on traite de la detection du plutonium dans des solutions de produits de fission emetteurs {beta} and {gamma}. On

  13. Plutonium, nuclear fuel; Le plutonium, combustible nucleaire

    Energy Technology Data Exchange (ETDEWEB)

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

    1960-07-01

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

  14. 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

  15. Study of High-Resolution Spectroscopy of Plutonium. Part I. Contribution to the Classification of the Arc Spectrum. Part II. Determination of the Magnetic Moment of {sup 239}Pu; Etude du plutonium par spectroscopie a haute resolution: contribution a la classification du spectre d'arc et determination du moment magnetique de {sup 239}Pu

    Energy Technology Data Exchange (ETDEWEB)

    Gerstenkorn, S

    1962-07-01

    The study of the hyperfine structure and isotope shift enabled the positions of the first five levels of the multiplet {sup 7}F{sub 0-6} belonging to the fundamental configuration 5f{sup 6}7s{sup 2} to be determined. The classification of the arc spectrum begun in this way led to 25 odd levels, the number of classified lines (70) representing about 30 p. 100 of the light emitted by this hollow cathode in the visible. In addition, the isotope shifts of many lines and the data given by the King furnace show that the first levels of the configuration 5f{sup 5}6d7s{sup 2} are also low less than 8000 cm{sup -1} above the fundamental level {sup 7}F{sub 0}. The proximity of the configuration f{sup 6}s{sup 2} and f{sup 5}ds{sup 2} shows that the bonding energies of the 5f and 6d electrons are of the same order of magnitude and this fact must be responsible for the multiple valences belonging to plutonium. From the hyperfine structure of spark lines (Pu II) the interval factor a{sub 7} for the electron was deduced giving for the calculated nuclear moment of {sup 239}Pu a value of +0.21 {+-}0.06 {mu}{sub N}. The position of the hyperfine components show that the nuclear moment is positive, although the theoretical value given by B. R. Mottelson and S. Nillson is negative and equal to -0.1 {mu}{sub N}. (author) [French] Partie 1 - L'etude des structures hyperfines et du deplacement isotopique des raies du spectre d'arc du plutonium a permis de determiner la position des cinq premiers niveaux du multiplet {sup 7}F{sub 0-6} correspondant a la configuration fondamentale 5f{sup 6}7s{sup 2}. Des lors, la classification du spectre d'arc du plutonium pouvait etre amorcee: 25 niveaux impairs ont ete mis en evidence et le nombre de raies classees (70) represente environ 30 p. 100 de l'intensite totale du spectre d'arc emis par une cathode creuse dans le visible. D'autre part, le deplacement isotopique de certaines raies, joint aux renseignements donnes par le spectre emis par le four

  16. Detection of {alpha} particles using semiconductors. Application to the control of plutonium extraction; Detection des particules {alpha} par semiconducteurs application au controle de l'extraction du plutonium

    Energy Technology Data Exchange (ETDEWEB)

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

    1968-03-01

    A study is made of a particles produced by thick sources, using either diffused junction or surface barrier semiconductor detectors for controlling continuously the plutonium extraction process. For this, a presenting apparatus is described in which the solutions to be analyzed flow in contact with the detector protected by a thin mica membrane. A method is described which gives a precise recording of the spectra and which thus allows the separation of two or more {alpha} emitters present in the same solution. This method has been applied to the measurement of {sup 239}Pu in the the presence of {sup 241}Am with an accuracy of {+-}5 per cent. In the second part of the report is considered the detection of plutonium in solutions of {beta} - {gamma} emitting fission products. Pile-up is reduced by using a fast amplification chain associated to totally depleted thin detectors. Under these conditions a few mg of {sup 239}Pu can be detected in solutions of fission products having an activity of 100 curies/liter. A method is given for discriminating {alpha} and {beta} particles, it is based on the difference in the collection times for the charges liberated by these particles in the detector. (author) [French] On etudie la detection de particules {alpha} issues de sources epaisses par detecteurs semiconducteurs a jonction diffusee ou a barriere de surface pour le controle continu du procede d'extraction du plutonium. A cet effet on decrit un appareil presentateur dans lequel les solutions a analyser circulent au contact du detecteur protege par une membrane mince de mica. On decrit une methode qui permet par le trace precis des spectres de separer deux ou plusieurs emetteurs {alpha} presents dans une meme solution. Cette methode a ete appliquee a la mesure du {sup 239}Pu en presence de {sup 241}Am avec une precision de {+-} 5 pour cent. Dans la deuxieme partie on traite de la detection du plutonium dans des solutions de produits de fission emetteurs {beta} and {gamma

  17. Isotopic analysis of plutonium by optical spectroscopy; Analyse isotopique du plutonium par spectroscopie optique

    Energy Technology Data Exchange (ETDEWEB)

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

    1961-07-01

    Isotopic analysis of mixtures of plutonium 239 and 240 has been carried out by means of the photo-electric spectrometer Fabry-Perot, the source being a hollow cathode cooled by liquid nitrogen. This first research has been concerned with finding among the spectral lines given by the hollow cathode, those suitable for use in analysis. Actually, the relative precision is of the order of 2 per cent (for samples containing 3 per cent of {sup 240}Pu). The study of the reproducibility of the measurements should make it possible to increase the precision; the relative precision which can be expected from this method should be 1 per cent for mixtures containing 1 per cent of {sup 240}Pu. (author) [French] L'analyse isotopique des melanges de plutonium 239 et 240 a ete effectuee a l'aide du spectrometre photoelectrique Fabry-Perot, la source etant une cathode creuse refroidie a l'azote liquide. Ce premier travail a eu pour but de discerner parmi les raies spectrales emises par la cathode creuse, celles susceptibles de servir de raies d'analyse. Actuellement, la precision relative est de l'ordre de 2 pour cent (pour des echantillons contenant 3 pour cent de {sup 240}Pu). L'etude de la reproductibilite des mesures devrait permettre d'ameliorer la precision; la precision relative que l'on pourrait atteindre par cette methode serait de 1 pour cent pour des melanges contenant 1 pour cent de {sup 240}Pu. (auteur)

  18. Study of the magnetic susceptibilities of some plutonium derivatives; Etude des susceptibilites magnetiques de quelques derives du plutonium

    Energy Technology Data Exchange (ETDEWEB)

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

    1969-06-01

    We present a detailed description of an automatic recording apparatus for magnetic susceptibility measurement of radioactive samples in the temperature range 4 K - 1200 K. We have measured the magnetic susceptibility of various plutonium compounds: - PuO{sub 2}, Pu{sub 2}O{sub 3}, PuO{sub 2-x}, - PuS, Pu{sub 2}S{sub 3}, Pu{sub 3}S{sub 4}, (U{sub x}Pu{sub 1-x})S - PuN - PuC{sub 1-x}(N,O,H,vacancy), Pu{sub 2}C{sub 3}, (U{sub 0.85}Pu{sub 0.15})C. The curves of susceptibilities versus temperature show many magnetic transitions. The interpretation of these results shows the existence of magnetic moments carried by the 5 f electrons and localized on the metallic sites as well as the great influence of the 'crystal field' in all these compounds. (author) [French] Nous decrivons d'une facon detaillee un appareil permettant de mesurer d'une facon continue et automatique des susceptibilites magnetiques sur des echantillons radioactifs dans un domaine de temperature s'etalant de 4 K a 1200 K. Nous avons mesure les susceptibilites magnetiques de certains composes du plutonium tels que: - PuO{sub 2}, Pu{sub 2}O{sub 3}, PuO{sub 2-x} - PuS, Pu{sub 2}S{sub 3}, Pu{sub 3}S{sub 4}, (U{sub x}Pu{sub 1-x})S - PuN - PuC{sub 1-x}(N,O,H,vacancy), Pu{sub 2}C{sub 3}, (U{sub 0.85}Pu{sub 0.15})C. Les courbes de susceptibilite magnetique en fonction de la temperature mettent en evidence de nombreuses transitions magnetiques. L'interpretation de ces resultats a montre l'existence de moments magnetiques portes par les electrons f et localises sur les sites metalliques ainsi que l'influence tres grande du champ cristallin. (auteur)

  19. Recommended plutonium release fractions from postulated fires. Final report

    International Nuclear Information System (INIS)

    Kogan, V.; Schumacher, P.M.

    1993-12-01

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

  20. Plutonium Protection System (PPS). Volume 2. Hardware description. Final report

    International Nuclear Information System (INIS)

    Miyoshi, D.S.

    1979-05-01

    The Plutonium Protection System (PPS) is an integrated safeguards system developed by Sandia Laboratories for the Department of Energy, Office of Safeguards and Security. The system is designed to demonstrate and test concepts for the improved safeguarding of plutonium. Volume 2 of the PPS final report describes the hardware elements of the system. The major areas containing hardware elements are the vault, where plutonium is stored, the packaging room, where plutonium is packaged into Container Modules, the Security Operations Center, which controls movement of personnel, the Material Accountability Center, which maintains the system data base, and the Material Operations Center, which monitors the operating procedures in the system. References are made to documents in which details of the hardware items can be found

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

    Energy Technology Data Exchange (ETDEWEB)

    ULLAH, M K

    2001-02-26

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

  2. Dresden 1 plutonium recycle program. Final report

    International Nuclear Information System (INIS)

    Bresnick, S.D.

    1980-01-01

    This is the final report on the Dresden 1 Plutonium Recycle Demonstration Program. It covers the work performed from July 1, 1978 to completion, which includes in-pool inspection of two fuel assemblies, removal of two fuel rods, and post-irradiation examination (PIE) of six fuel rods. Appendix A describes the inspection and rod removal operations, and Appendix B describes the PIE work

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1960-07-01

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

  4. Plutonium fires; Incendies de plutonium

    Energy Technology Data Exchange (ETDEWEB)

    Mestre, E.

    1959-06-23

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1960-07-01

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

  6. Measurement of the {sup 240}Pu concentration of a plutonium sample by the spontaneous fission method (1960); Mesure de la teneur d'un plutonium en {sup 240}Pu par la methode des fissions spontanees (1960)

    Energy Technology Data Exchange (ETDEWEB)

    Caizergues, R; Clouet d' Orval, C [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

    1960-07-01

    It is very important to know the plutonium-240 content of the plutonium formed in piles. The method of measurement described here consists in counting the number of spontaneous fissions produced in a known quantity of plutonium. This measurement is carried out in a multiple-plate ionisation chamber, the plutonium being deposited on the plates. The disintegration constant of plutonium-240 by spontaneous fission being known the plutonium-240 content in the sample can be calculated. (author) [French] La connaissance de la teneur en plutonium-240 du plutonium forme dans les piles est une question importante. La methode de mesure presentee ici consiste a compter le nombre de fissions spontanees issues d'une quantite connue de plutonium. Cette mesure est effectuee dans une chambre d'ionisation a plateaux multiples sur lesquels est depose le plutonium. La connaissance de la constante de desintegration du plutonium-240 par fissions spontanees permet de calculer la teneur en plutonium-240. (auteur)

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

    Energy Technology Data Exchange (ETDEWEB)

    Leguay, N.

    2011-07-01

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

  8. Estimation of the Body Content Following Inhalation of Insoluble Plutonium; Evaluation de la Charge Corporelle de Plutonium, a la Suite de l'Inhalation de Plutonium Insoluble; 041e 041f 0420 0415 0414 ; Carga Corporal Consecutiva a la Inhalacion de Plutonio Insoluble

    Energy Technology Data Exchange (ETDEWEB)

    Dolphin, G. W. [Authority Health and Safety Branch, Radiological Protection Division, United Kingdom Atomic Energy Authority, Harwell, Berks. (United Kingdom)

    1964-11-15

    The problem of estimating the body content of plutonium following the inhalation of plutonium oxide is of considerable practical importance and, on the grounds of the known insolubility of plutonium oxide, measurements of plutonium in urine might be considered valueless. This paper reviews the relevant published biological data from beagle dog experiments and also reviews data from two human cases. From this review it is concluded that there is evidence for believing that the body content, following an accidental inhalation, can be estimated from the measurements of plutonium excreted in urine at times greater than about 300 d after the intake. Some possible excretion methods are discussed. Finally, there is a comment on the radiological protection aspects of insoluble plutonium in the lungs and bronchial lymph nodes and it is stressed that the particular nature of the plutonium must be taken into consideration. (author) [French] Le probleme de l'evaluation de la charge corporelle de plutonium a la suite de l'inhalation d'oxyde de plutonium presente une grande importance sur l'e plan pratique et, en raison de l'insolubilite bien connue de l'oxyde de plutonium on peut etre tente de considerer comme sans valeur les dosages du plutonium contenu dans l'urine. L'auteur passe en revue les donnees biologiques pertinentes deja publiees a la suite d'experiences faites sur les chiens bigles, ainsi que des donnees relatives a deux cas d'inhalation par des hommes. D'apres cette etude, il y a lieu de croire qu'on peut evaluer la charge corporelle de plutonium, a la suite d'une inhalation accidentelle, en faisant des dosages du plutonium contenu dans l'urine plus de 300 jours apres l'absorption. Il discute plusieurs methodes possibles. Il examine, enfin, sous l'angle de la protection radiologique, la presence du plutonium insoluble dans les poumons et les ganglions lymphatiques des bronches et il insiste sur le fait qu'il faut tenir compte de la nature particuliere du plutonium

  9. Solutions to criticality problems in a plutonium extraction plant; Solutions apportees aux problemes de criticite d'une usine d'extraction du plutonium

    Energy Technology Data Exchange (ETDEWEB)

    Jouannaud, C; Rodier, J; Fruchard, Y; Peyresblanques, H; Papault, C; Tabardel-Brian, R [Commissariat a l' Energie Atomique, Chusclan (France). Centre de Production de Plutonium de Marcoule, service d' extraction du plutonium, service de protection contre les radiations et d' assainissement radioactif

    1968-08-01

    There are two aspects to nuclear criticality safety: prevention of criticality and protection against the consequences of a possible accident: this report considers these two aspects in the case of the Marcoule Plutonium Extraction Plant. After briefly recalling the various techniques used for avoiding criticality (mass, geometry, concentration, poisoning), the authors describe their application in the plant and show in particular that, a rational use of a favorable geometry is a factor both for security and from an economic point of view. The authors then describe the inside organisation which makes it possible to obtain the necessary intrinsic safety standard right from the advance project stage, and to control the workshop safety during the operation of the plant. The second part of the report deals with the system of protection against the consequences of a possible accident: definition of a typical accident, fixing of the boundaries of a critical zone, safety alarm device, individual and collective dosimetry, evacuation plan and safety instructions. (authors) [French] La securite vis-a-vis des risques de criticite revet deux aspects: la prevention de la criticite et la protection contre les consequences d'un accident eventuel: le present rapport developpe ces deux aspects dans le cas de l'Usine d'Extraction du Plutonium de Marcoule. Apres avoir rappele les differentes techniques de prevention de la criticite (masse, geometrie, concentration, empoisonnement), les auteurs decrivent leur application a l'Usine et montrent notamment que l'utilisation rationnelle de la geometrie favorable est un double facteur de securite et d'economie. Les auteurs decrivent ensuite l'organisation interieure qui permet de realiser la securite intrinseque des le stade d'un avant projet et de controler la securite des ateliers au cours de la vie de l'Usine. La deuxieme partie du rapport est consacree au systeme de protection contre les consequences d'un accident eventuel: definition d

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

    International Nuclear Information System (INIS)

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

    1977-05-01

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

  11. Study of the physico-chemical agents influencing uranium and plutonium extraction by tributylphosphate in nitric media; Etude des facteurs physico-chimiques intervenant dans l'extraction de l'uranium et du plutonium par le phosphate de tributyle en milieu nitrique

    Energy Technology Data Exchange (ETDEWEB)

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

    1967-03-01

    The following different factors are reviewed: tributylphosphate concentration, nitric acid concentration, influence of non-extractable nitrates, simultaneous presence of uranium and plutonium, presence of some different ions, temperature, nature of the diluent, addition of a second active solvent (synergic or antagonistic effect), tributylphosphate and diluent degradation. (author) [French] On passe en revue les differents facteurs suivants: concentration en phosphate de tributyle, concentration en acide nitrique, influence des nitrates non-extractibles, presence simultanee d'uranium et de plutonium, presence d'ions divers, addition d'un second solvant actif (effet de synergie, ou effet antagoniste), degradation du phosphate de tributyle et des solvants inertes. (auteur)

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1965-07-01

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

  13. Decontamination of Battelle-Columbus' Plutonium Facility. Final report

    International Nuclear Information System (INIS)

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

    1984-01-01

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

  14. Final results of the PIDIE intercomparison exercise for the plutonium isotopic determination by gamma-ray spectrometry

    International Nuclear Information System (INIS)

    Morel, J.; Chauvenet, B.; Etcheverry, M.

    1991-01-01

    Final results from the PIDIE intercomparison exercise organised by the ESARDA Working Group on techniques and standards for non-destructive analysis are presented. The aim of this exercise carried out in 1988 was to test the gamma-ray spectroscopy methods used to determine the plutonium isotopic ratios in a large range of isotopic composition, in order to analyse the parameters and the error sources influencing the results. Sets of seven sealed samples of different plutonium isotopic composition were sent to nine participating laboratories. The final results with uncertainty indicators are reported; they are compared with complementary mass-spectrometry determinations. No important bias has been observed from this exercise. Significant improvements in plutonium isotopic determination by gamma-ray spectrometry come from both more elaborate spectrum analysis methods and better equipment

  15. Studies of plutonium-iron and uranium-plutonium-iron alloys; Etudes d'alliages plutonium-fer et d'alliages uranium-plutonium-fer

    Energy Technology Data Exchange (ETDEWEB)

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

    1964-01-15

    We study the plutonium-iron system, by means of dilatometry, X rays and metallography, especially in the domain between PuFe{sub 2} and Fe. We determine the solubilities of Fe in PuFe{sub 2} and of Pu in Fe. We show the presence of an hexagonal PuFe{sub 2} phase and we propose a modification in the Pu-Fe phase diagram. Some low iron concentration U-Pu-Fe alloys have also been investigated. We characterise the different phases. We confirm that adding some iron lowers the quantity of the zeta U-Pu phase. We emphasize some characteristics of the alloys having the global concentration (U, Pu){sub 6} Fe. (authors) [French] On etudie par dilatometrie, rayons X et micrographie le systeme plutonium-fer, principalement dans la region comprise entre PuFe{sub 2} et Fe, On determine les solubilites du fer dans PuFe{sub 2}, et de Pu dans Fe. On met en evidence une phase PuFe{sub 2} hexagonale et on propose une modification du diagramme d'equilibre Pu-Fe. Certains alliages U-Pu-Fe a faibles concentrations en fer sont egalement etudies. On caracterise les phases en presence. On confirme que l'addition de fer diminue rapidement la quantite de phase U-Pu zeta. Enfin on revele certaines caracteristiques des alliages de composition globale (U, Pu){sub 6} Fe. (auteurs)

  16. Biological Monitoring for Plutonium-241; Detection du Plutonium-241 par Controles Biologiques; Dozimetriya Plutoniya-241 v biologicheskikh materialakh; Determinacion del Plutonio-241 en Sustancias Biologicas

    Energy Technology Data Exchange (ETDEWEB)

    Dalton, J. C.; McDonald, B. J.; Barnes, V. [United Kingdom Atomic Energy Authority, Windscale Works, Sellafield (United Kingdom)

    1965-10-15

    ) [French] Les auteurs indiquent l'origine et les caracteristiques du {sup 241}Pu, en examinant plus particulierement les risques qu'il presente pour la sante et le probleme que pose son dosage. Ils decrivent un systeme de comptage, qui est en voie d'elaboration a Windscale, pour doser de petites quantites de {sup 241}Pu dans des echantillons preleves dans le cadre d'un programme de controle biologique. Au stade actuel de sa mise au point, cette methode est pour le moins aussi sensible que les procedes signales anterieurement et elle est plus simple, plus rapide et plus rentable. Elle est essentiellement destinee aux analyses d'urine en vue de completer les renseignements deja obtenus par analyse autoradiographique des isotopes emetteurs alpha du plutonium. Le meme porte-source est utilise pour le dosage du {sup 241}Pu, ce qui permet d'eviter certains travaux preparatoires. A l'aide d'une methode fondee sur l'echange d'anions, les isotopes du plutonium sont tout d'abord separes de l'echantillon d'urine ou de toute autre matiere biologique, dans un etat de grandepurete radiochimique. Puis on les fixe par electrolyse sur un disque en acier inoxydable. Un systeme de comptage par anticoiencidence comportant un compteur proportionnel de faible volume a circulation continue de gaz et muni d'une garde anticoiencidence a scintillation en matiere plastique permet de determiner directement le spectre beta mou du {sup 241}Pu (energie maximale 20 keV, periode 13,3 a). Les dimensions sont telles que toutes les particules beta emises par le plutonium sont absorbees a l'interieur du compteur proportionnel alors que les particules alpha perdent 50% environ de leur energie dans le scintillateur en matiere plastique. Pour les deux rayonnements, la geometrie est pratiquement 2{pi}. A son stade actuel, le materiel permet de detecter 3 pCi de {sup 241}Pu en 1 h de comptage. Cela correspond au taux d'excretion urinaire de 24 h trois mois apres l'absorption d'environ 5% de la charge corporelle

  17. Study of uranium-plutonium alloys containing from 0 to 20 peri cent of plutonium (1963); Etude des alliages uranium-plutonium aux concentrations comprises entre 0 et 20 pour cent de plutonium (1963)

    Energy Technology Data Exchange (ETDEWEB)

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

    1963-05-15

    The work is carried out on U-Pu alloys in the region of the solid solution uranium alpha and in the two-phase region uranium alpha + the zeta phase. The results obtained concern mainly the influence of the addition of plutonium on the physical properties of the uranium (changes in the crystalline parameters, the density, the hardness) in the region of solid solution uranium alpha. In view of the discrepancies between various published results as far as the equilibrium diagram for the system U-Pu is concerned, an attempt was made to verify the extent of the different regions of the phase diagram, in particular the two phased-region. Examinations carried out on samples after various thermal treatments (in particular quenching from the epsilon phase and prolonged annealings, as well as a slow cooling from the epsilon phase) confirm the results obtained at Los Alamos and Harwell. (author) [French] L'etude porte sur des alliages U-Pu du domaine de la solution solide uranium alpha et du domaine biphase uranium + phase zeta. Les resultats obtenus concernent en premier lieu l'influence de l'addition de plutonium sur les proprietes physiques de l'uranium (changement des parametres cristallins, densite, durete) dans le domaine de la solution solide uranium alpha. Compte tenu des divergences entre les differents resultats publies en ce qui concerne le diagramme d'equilibre du systeme U-Pu, on a essaye ensuite de verifier l'etendue des differents domaines du diagramme des phases, en particulier du domaine biphase zeta + uranium alpha. Les examens par micrographie et par diffraction des rayons X des echantillons apres differents traitements thermiques (notamment trempe a partir de la phase epsilon et recuits prolonges, ainsi qu'un refroidissement lent etage a partir de la phase epsilon) confirment les resultats obtenus a Los Alamos et a Harwell. (auteur)

  18. The production control laboratories of the plutonium extraction Plant at Marcoule. Six years operating experience: 1957 - 1963; Les laboratoires de fabrication de l'usine d'extraction du plutonium de Marcoule. Experience des 6 premieres annees de fonctionnement: 1957 - 1963

    Energy Technology Data Exchange (ETDEWEB)

    Fontaine, A [CEA Marcoule, Centre de Production de Plutonium, 30 (France)

    1964-07-01

    In this paper, the author attempts to sum up the conditions prevailing, after six years of operation, in the Laboratories of the Plutonium Extraction Plant. The origins and objectives are briefly reviewed, the technology and staff recruitment policy are examined, and progress made is shown. The methods used as well as the scope of application and limits imposed at the present state are considered. Past achievements and further possibilities in the next future are examined. An attempt has been made to bring out the outlooks for the more distant future and to investigate the conditions required for the successful carrying out of the program. (author) [French] Le present rapport tente, apres 6 ans de vie, de faire le point de la situation des Laboratoires du Service Extraction du Plutonium. Apres un rapide retour sur les origines et les objectifs, apres quelques considerations sur le recrutement et la technologie situant le contexte de leurs progres, nous etudierons les methodes, leurs domaines d'application, leurs limites actuelles. Nous ferons un bilan des realisations et des possibilites pour un avenir proche. Nous tenterons de degager quelques vues plus lointaines et les conditions pour les mener a bonne fin. (auteur)

  19. Design of an integrated non-destructive plutonium assay facility

    International Nuclear Information System (INIS)

    Moore, C.B.

    1984-01-01

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

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

    International Nuclear Information System (INIS)

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

    1986-12-01

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

  1. Plutonium Finishing Plant

    Data.gov (United States)

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

  2. 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)

  3. Solutions to criticality problems in a plutonium extraction plant; Solutions apportees aux problemes de criticite d'une usine d'extraction du plutonium

    Energy Technology Data Exchange (ETDEWEB)

    Jouannaud, C.; Rodier, J.; Fruchard, Y.; Peyresblanques, H.; Papault, C.; Tabardel-Brian, R. [Commissariat a l' Energie Atomique, Chusclan (France). Centre de Production de Plutonium de Marcoule, service d' extraction du plutonium, service de protection contre les radiations et d' assainissement radioactif

    1968-08-01

    There are two aspects to nuclear criticality safety: prevention of criticality and protection against the consequences of a possible accident: this report considers these two aspects in the case of the Marcoule Plutonium Extraction Plant. After briefly recalling the various techniques used for avoiding criticality (mass, geometry, concentration, poisoning), the authors describe their application in the plant and show in particular that, a rational use of a favorable geometry is a factor both for security and from an economic point of view. The authors then describe the inside organisation which makes it possible to obtain the necessary intrinsic safety standard right from the advance project stage, and to control the workshop safety during the operation of the plant. The second part of the report deals with the system of protection against the consequences of a possible accident: definition of a typical accident, fixing of the boundaries of a critical zone, safety alarm device, individual and collective dosimetry, evacuation plan and safety instructions. (authors) [French] La securite vis-a-vis des risques de criticite revet deux aspects: la prevention de la criticite et la protection contre les consequences d'un accident eventuel: le present rapport developpe ces deux aspects dans le cas de l'Usine d'Extraction du Plutonium de Marcoule. Apres avoir rappele les differentes techniques de prevention de la criticite (masse, geometrie, concentration, empoisonnement), les auteurs decrivent leur application a l'Usine et montrent notamment que l'utilisation rationnelle de la geometrie favorable est un double facteur de securite et d'economie. Les auteurs decrivent ensuite l'organisation interieure qui permet de realiser la securite intrinseque des le stade d'un avant projet et de controler la securite des ateliers au cours de la vie de l'Usine. La deuxieme partie du rapport est consacree au systeme de protection contre les

  4. Preventive arms control. Case study: plutonium disposition. Final report

    International Nuclear Information System (INIS)

    Liebert, W.

    2001-01-01

    Plutonium stored in separated form poses a severe threat of nuclear weapons proliferation. While options for the disposition of military plutonium stockpiles have been studied for several years, similar work has hardly been undertaken for plutonium stockpiles in the civilian sector. In the framework of this project, the various options to dispose of stockpiles of separated plutonium in the civilian sector were to be investigated. The project was embedded in the FONAS-project network on Preventive Arms Control, and the findings of this study were to be considered for the development of a concept of Preventive Arms Control. As a first step, the internationally available information on different options for plutonium disposition (MOX-use, immobilization together with radioactive wastes, elimination) were collected and compiled to allow further assessment of the different options. For some of the options, technical questions were examined in more detail. For this purpose, neutron transport and fuel burnup calculations were performed. In particular, the analysis focused on concepts for the elimination of plutonium by the use of uranium-free fuel in existing light-water reactors, since they are particularly attractive from the point of view of non-proliferation. The calculations were performed for a reference fuel based on yttrium-stabilized zirconia, with parameters like the initial plutonium content or the use of burnable neutron poisons varying. A systematic and complete analysis of the performed calculations, however, could not be undertaken due to project time restrictions. On the basis of assessment criteria for Preventive Arms Control developed by the project network, a specific set of criteria for the assessment of the pros and cons of different plutonium disposition methods has been defined. These criteria may then be used as part of a concept of prospective technology assessment. The project findings present a starting base for a comprehensive assessment of the

  5. The reprocessing of irradiated fuels improvement and extension of the solvent extraction process; Le traitement des combustibles irradies amelioration et extension du procede utilisant les solvants

    Energy Technology Data Exchange (ETDEWEB)

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

    1964-07-01

    Improvements made in the conventional tri-butylphosphate process are described, in particular. the concentration and the purification of plutonium by one extraction cycle using tri-butyl-phosphate with reflux; and the use of an apparatus working continuously for precipitating plutonium oxalate, for calcining the oxalate, and for fluorinating the oxide. The modifications proposed for the treatment of irradiated uranium - molybdenum alloys are described, in particular, the dissolution of the fuel, and the concentration of the fission product solutions. The solvent extraction treatment is used also for the plutonium fuels utilized for the fast breeder reactor (Rapsodie) An outline of the process is presented and discussed, as well as the first experimental results and the plans for a pilot plant having a capacity of 1 kg/day. The possible use of tn-lauryl-amine in the plutonium purification cycle is now under consideration for the processing plant at La Hague. The flowsheet for this process and its performance are presented. The possibility of vitrification is considered for the final treatment of the concentrated radioactive wastes from the Marcoule (irradiated uranium) and La Hague (irradiated uranium-molybdenum) Centers. Three possible processes are described and discussed, as well as the results obtained from the operation of the corresponding experimental units using tracers. (authors) [French] On decrit les ameliorations apportees au procede classique utilisant le phosphate tributylique, et notamment la concentration et la purification du plutonium par un cycle d'extraction au tributylphosphate avec reflux, l'utilisation d'un appareillage continu de precipitation d'oxalate de plutonium, de calcination de l'oxalate, et de fluoration de l'oxyde. On presente les modifications envisagees pour le traitement des alliages uranium-molybdene irradies, principalement en ce qui concerne la dissolution du combustible et la concentration des solutions de produits de fission

  6. Plutonium disposition study phase 1b final report

    International Nuclear Information System (INIS)

    1993-01-01

    This report provides the results of the Westinghouse activities performed as part of the Plutonium Disposition Study Phase 1b. These activities, which took place from May 16, 1993 to September 15, 1993, build upon the work completed in Phase 1a, which concluded on May 15, 1993. In Phase 1a, three Plutonium Disposal Reactor (PDR) options were developed for the disposal of excess weapons grade plutonium from returned and dismantled nuclear weapons. This report documents the results of several tasks that were performed to further knowledge in specific areas leading up to Phase 2 of the PDR Study. The Westinghouse activities for Phase 1b are summarized as follows: (1) resolved technical issues concerning reactor physics including equilibrium cycle calculations, use of gadolinium, moderator temperature coefficient, and others as documented in Section 2.0; (2) analyzed large Westinghouse commercial plants for plutonium disposal; (3) reactor safety issues including the steam line break were resolved, and are included in Section 2.0; (4) several tasks related to the PDR Fuel Cycle were examined; (5) cost and deployment options were examined to determine optimal configuration for both plutonium disposal and tritium production; (6) response to questions from DOE and National Academy of Scientists (NAS) reviewers concerning the PDR Phase 1a report are included in Appendix A

  7. Technique of preparation of plutonium screens for soft x ray spectrography (1963); Technique de preparation d'ecrans de plutonium pour la spectrographie de rayons x mous (1963)

    Energy Technology Data Exchange (ETDEWEB)

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

    1963-07-01

    The present work concerns the preparation of thin layers of pure plutonium (thickness 100 to 10000 A) by thermal vacuum evaporation. The protection of the plutonium against oxidation is obtained by vacuum deposition of aluminium layers under. and above the plutonium layer. The purity of the layers is checked by electron and X ray diffraction which has shown that very thin films of plutonium condense in {beta} form instead of {alpha}. (author) [French] Le present travail concerne la preparation de couches minces (epaisseurs de 100 a 10000 A) de plutonium pur par evaporation thermique sous vide. La protection du plutonium contre l'oxydation par l'air est obtenu grace a des couches d'aluminium deposees sous vide sous et sur la couche de plutonium. La purete des couches est verifiee par diffraction d'electrons et de rayons X ce qui a permis d'observer que les couches tres minces de plutonium se condensent en phase {beta} au lieu de la phase {alpha}. (auteur)

  8. Plutonium in the environment - bibliographic study and quantification; Impacts environnemental et sanitaire des isotopes du plutonium, etude bibliographique et quantification

    Energy Technology Data Exchange (ETDEWEB)

    Guetat, Ph; Monfort, M; Ansoborlo, E [CEA Marcoule, Dir. de l' Energie Nucleaire, 30 (France); Bion, L; Moulin, V; Reiller, P; Vercouter, Th [CEA Saclay, Dir. de l' Energie Nucleaire, 91 - Gif sur Yvette (France); Boucher, L; Jourdain, F; Van Dorpe, F [CEA Cadarache, Dir. de l' Energie Nucleaire, 13 - Saint Paul lez Durance (France); Comte, A; Flury Heard, A; Fritsch, P; Menetrier, F [CEA Fontenay-aux-Roses, Dir. des Sciences du Vivant, 92 (France)

    2008-07-01

    This document deals with the different isotopes of plutonium. It intends to summarize the main features of plutonium behaviour from sources inside installation to the environment and man, and is expected to report the current knowledge about the different parameters used in the models for environmental and radiological impact assessment. The objective is to gather scientific information useful for deciders in case of accident or for regulation purposes. It gives main information on radiological and chemical characteristics which are necessary to understand transfers between compartments. Then it reports information on normal and accidental historical sources and present releases. The next part deals with transfer parameters in the installations and in environment. Parameters that influence its behaviour are examined, inside installations (physico-chemical forms and events that lead to releases), and outside in the environment for deposition to soils and transfer to plants, and animal products. A full chapter is dedicated to presentation of typical assessments, for each isotope and for mixture, and correspondence between activity, mass and dose reference levels are presented and discussed. Transfer and behaviour in man and effects on health are finally presented. (author)

  9. Study of the solubility of plutonyl nitrate with a view to its extraction by a solvent; Etude de la solubilite du nitrate de plutonyle en vue de son extraction par solvant

    Energy Technology Data Exchange (ETDEWEB)

    Vergnaud, G [Commissariat a l' Energie Atomique, Fontenay aux Roses (France). Centre d' Etudes Nucleaires

    1965-09-01

    The research covers the determination of the partition coefficient of plutonyl nitrate and their application to the industrial treatment of plutonium. The solvent used is a tri-n-butyl phosphate solution diluted to 30 per cent in dodecane. The parameters which have been studied and which can affect the extraction of the plutonyl nitrate are: the plutonyl nitrate concentration; the nitric acid concentration; the uranyl nitrate concentration; the tetravalent plutonium nitrate concentration. The industrial application has been studied using a battery of mixer-separators. The operational conditions are defined in the case of a conventional plutonium separation plant. The results obtained, for a higher plutonyl nitrate concentration than that actually planned, are satisfactory and encouraging as far as the operation is concerned. Only the presence of polymerized tetravalent plutonium can adversely affect the satisfactory extraction of the plutonium. (author) [French] L'etude porte sur les coefficients de partage du nitrate de plutonyle et leur application a l'elaboration industrielle du plutonium. Le solvant utilise est une solution de phosphate de tri-n-butyle, dilue a 30 pour cent dans le dodecane. Les parametres etudies et pouvant influencer l'extraction du nitrate de plutonyle, par ce solvant, sont: concentration du nitrate de plutonyle; concentration de l'acide nitrique; concentration du nitrate d'uranyle; concentration au nitrate de plutonium tetravalent. L'application industrielle est etudiee au moyen d'une batterie de melangeurs-decanteurs. Les conditions operatoires sont definies d'apres un schema classique d'usine de separation de plutonium. Les resultats obtenus, pour une concentration du nitrate de plutonyle superieure a celle reellement prevue, sont satisfaisants et encourageants pour l'exploitation. Seule, la presence de plutonium tetraralent polymerise, peut nuire a une bonne extraction du plutonium. (auteur)

  10. Study of the solubility of plutonyl nitrate with a view to its extraction by a solvent; Etude de la solubilite du nitrate de plutonyle en vue de son extraction par solvant

    Energy Technology Data Exchange (ETDEWEB)

    Vergnaud, G. [Commissariat a l' Energie Atomique, Fontenay aux Roses (France). Centre d' Etudes Nucleaires

    1965-09-01

    The research covers the determination of the partition coefficient of plutonyl nitrate and their application to the industrial treatment of plutonium. The solvent used is a tri-n-butyl phosphate solution diluted to 30 per cent in dodecane. The parameters which have been studied and which can affect the extraction of the plutonyl nitrate are: the plutonyl nitrate concentration; the nitric acid concentration; the uranyl nitrate concentration; the tetravalent plutonium nitrate concentration. The industrial application has been studied using a battery of mixer-separators. The operational conditions are defined in the case of a conventional plutonium separation plant. The results obtained, for a higher plutonyl nitrate concentration than that actually planned, are satisfactory and encouraging as far as the operation is concerned. Only the presence of polymerized tetravalent plutonium can adversely affect the satisfactory extraction of the plutonium. (author) [French] L'etude porte sur les coefficients de partage du nitrate de plutonyle et leur application a l'elaboration industrielle du plutonium. Le solvant utilise est une solution de phosphate de tri-n-butyle, dilue a 30 pour cent dans le dodecane. Les parametres etudies et pouvant influencer l'extraction du nitrate de plutonyle, par ce solvant, sont: concentration du nitrate de plutonyle; concentration de l'acide nitrique; concentration du nitrate d'uranyle; concentration au nitrate de plutonium tetravalent. L'application industrielle est etudiee au moyen d'une batterie de melangeurs-decanteurs. Les conditions operatoires sont definies d'apres un schema classique d'usine de separation de plutonium. Les resultats obtenus, pour une concentration du nitrate de plutonyle superieure a celle reellement prevue, sont satisfaisants et encourageants pour l'exploitation. Seule, la presence de plutonium tetraralent polymerise, peut nuire a une bonne extraction du plutonium

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

    International Nuclear Information System (INIS)

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

    1989-01-01

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

  12. Study of immiscibilities in the trilaurylamine - dodecane - nitric acid - plutonium system; Etude des immiscibilites dans le systeme trilaurylamine - dodecane - acide nitrique - plutonium

    Energy Technology Data Exchange (ETDEWEB)

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

    1968-07-01

    Phase equilibrium in systems made up of trilaurylamine, dodecane, nitric acid tetravalent plutonium is shown by drawing the triangular diagrams. the study of these diagrams provides informations concerning the causes of immiscibility. Heterogeneity of the organic mixtures can be related to some characteristics of the components- dipole moment, molecular polarizability and hydrogen bond exchanging ability-Depending on these, some rules may be established which can be used to make a proper choice of an additive in order to improve the miscibility. As an application a study on the partial substitution of dodecane with decalin, in plutonium extraction experiments, has been done showing a possible improvement of the extraction process. (author) [French] L equilibre des phases dans les systemes formes a partir de trilaurylamine, de dodecane, d'acide nitrique et de plutonium tetravalent est represente en tracant les diagrammes triangulaires. L'examen de ces diagrammes permet d'apporter certaines precisions en ce qui concerne l'origine des immiscibilites. Celles ci sont ensuite reliees a certaines caracteristiques des constituants: le moment dipolaire, la polarisabilite moleculaire et la tendance a former des liaisons hydrogene. Sur les memes bases, il est possible d'etablir un certain nombre de regles pouvant servir a guider le choix d'un additif ameliorant la miscibilite. En application, une etude sur le remplacement partiel du dodecane par la decaline montre l'interet de l'emploi de ce compose dans le procede de purification du plutonium. (auteur)

  13. Dynamic process model of a plutonium oxalate precipitator. Final report

    Energy Technology Data Exchange (ETDEWEB)

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

    1977-11-01

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

  14. Dynamic process model of a plutonium oxalate precipitator. Final report

    International Nuclear Information System (INIS)

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

    1977-11-01

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

  15. Reaction of uranium and plutonium carbides with nitrogen; Reaction avec l'azote des carbures d'uranium et de plutonium

    Energy Technology Data Exchange (ETDEWEB)

    Lorenzelli, R; Martin, A; Schickel, R [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1966-03-01

    Uranium and plutonium carbides react with nitrogen during the grinding process preceding the final sintering. The reaction occurs even in argon atmospheres containing a few percent of residual nitrogen. The resulting contamination is responsible for the appearance of an equivalent quantity of higher carbide in the sintered products; nitrogen remains quantitatively in the monocarbide phase. UC can be transformed completely into nitride under a nitrogen pressure, at a temperature as low as 400 C. The reaction is more sluggish with PuC. The following reactions take places: UC + 0,8 N{sub 2} {yields}> UN{sub 1.60} + C and PuC + 0,5 N{sub 2} {yields} PuN + C. (authors) [French] Les carbures d'uranium et de plutonium reagissent avec l'azote au cours du broyage qui precede le frittage final. Cette reaction est sensible meme sous des atmospheres d'argon ne contenant que quelques pour cent d'azote. Cette contamination se traduit sur les produits frittes par l'apparition d'une quantite equivalente de carbure superieur, l'azote restant fixe quantitativement dans la phase monocarbure. On peut transformer entierement UC en nitrure par action de l'azote sous pression des 400 C. La reaction est plus difficile avec PuC. Les reactions sont les suivantes: UC + 0,8 N{sub 2} {yields} UN{sub 1.60} + C et PuC + 0,5 N{sub 2} {yields} PuN + C.

  16. Metabolism and toxicology of plutonium-239 - evaluation of the internal contamination of persons professionally exposed (1963); Metabolisme et toxicologie du plutonium 239 - evaluation de la contamination interne des personnes professionnellement exposees (1963)

    Energy Technology Data Exchange (ETDEWEB)

    Henry, Ph [Commissariat a l' Energie Atomique, Centre de Production de Plutonium, Marcoule (France). Centre d' Etudes Nucleaires

    1963-07-01

    After reviewing the main metabolic and toxicological properties of plutonium 239 as well as the professional norms now in force, the report considers the difficult problem of the evaluation of the internal contamination of persons professionally exposed. This evaluation is dependent on the practical organisation of the supervision involved: - systematic supervision by periodic analysis of urinary Pu and special supervision in the case of incidents by an examination adapted to each case. A simple interpretation of the systematic analyses, as well as the evaluation methods used in the main cases of occidental contamination are outlined. (author) [French] Apres avoir passe en revue les principales proprietes metaboliques et toxicologiques du plutonium 239, ainsi que les normes professionnelles actuellement en vigueur, le rapport aborde le probleme difficile de l'evaluation de la contamination interne des personnes professionnellement exposees. Cette evaluation est fonction de l'organisation pratique de la surveillance: - surveillance systematique par des analyses periodiques de Pu urinaire et surveillance speciale en cas d'incidents par des examens appropries a chaque cas. Une interpretation simple des analyses systematiques, ainsi que des methodes d'evaluation utilisables dans les principaux cas de contamination accidentelle sont exposees. (auteur)

  17. The transport of plutonium industry in France. A high risk activity; Les transports de l'industrie du plutonium en France. Une activite a haut risque. Resume de l'etude et rapport final

    Energy Technology Data Exchange (ETDEWEB)

    Coeytaux, X.; Faid, Y.B.; Hazemann, J.; Marignac, Y.; Schneider, M

    2003-02-15

    According to the estimations of the report more than 450 transport of materials including about 40 tons of plutonium circulate in France during one year. The nuclear matters transported are a source of danger. The risks in relation with the handling and transport of plutonium touch the criticality risk, its great toxicity, and the problem of proliferation. To these risks it is necessary to add terrorists attacks. Three scenarios of accidents have been developed to illustrate the risk potential. A scenario of train accident, with derailment in a tunnel then crash with an other train; a simple scenario occurring to a lorry of plutonium powder; then a scenario of an accident following a terrorist act. These scenarios should be studied by I.R.S.N and the results should be given to the public and to elected people confronted to the transport of plutonium. (N.C.)

  18. Plutonium Consumption Program, CANDU Reactor Project final report

    Energy Technology Data Exchange (ETDEWEB)

    1994-07-31

    DOE is investigating methods for long term dispositioning of weapons grade plutonium. One such method would be to utilize the plutonium in Mixed OXide (MOX) fuel assemblies in existing CANDU reactors. CANDU (Canadian Deuterium Uranium) reactors are designed, licensed, built, and supported by Atomic Energy of Canada Limited (AECL), and currently use natural uranium oxide as fuel. The MOX spent fuel assemblies removed from the reactor would be similar to the spent fuel currently produced using natural uranium fuel, thus rendering the plutonium as unattractive as that in the stockpiles of commercial spent fuel. This report presents the results of a study sponsored by the DOE for dispositioning the plutonium using CANDU technology. Ontario Hydro`s Bruce A was used as reference. The fuel design study defined the optimum parameters to disposition 50 tons of Pu in 25 years (or 100 tons). Two alternate fuel designs were studied. Safeguards, security, environment, safety, health, economics, etc. were considered. Options for complete destruction of the Pu were also studied briefly; CANDU has a superior ability for this. Alternative deployment options were explored and the potential impact on Pu dispositioning in the former Soviet Union was studied. An integrated system can be ready to begin Pu consumption in 4 years, with no changes required to the reactors other than for safe, secure storage of new fuel.

  19. Plutonium Consumption Program, CANDU Reactor Project final report

    International Nuclear Information System (INIS)

    1994-01-01

    DOE is investigating methods for long term dispositioning of weapons grade plutonium. One such method would be to utilize the plutonium in Mixed OXide (MOX) fuel assemblies in existing CANDU reactors. CANDU (Canadian Deuterium Uranium) reactors are designed, licensed, built, and supported by Atomic Energy of Canada Limited (AECL), and currently use natural uranium oxide as fuel. The MOX spent fuel assemblies removed from the reactor would be similar to the spent fuel currently produced using natural uranium fuel, thus rendering the plutonium as unattractive as that in the stockpiles of commercial spent fuel. This report presents the results of a study sponsored by the DOE for dispositioning the plutonium using CANDU technology. Ontario Hydro's Bruce A was used as reference. The fuel design study defined the optimum parameters to disposition 50 tons of Pu in 25 years (or 100 tons). Two alternate fuel designs were studied. Safeguards, security, environment, safety, health, economics, etc. were considered. Options for complete destruction of the Pu were also studied briefly; CANDU has a superior ability for this. Alternative deployment options were explored and the potential impact on Pu dispositioning in the former Soviet Union was studied. An integrated system can be ready to begin Pu consumption in 4 years, with no changes required to the reactors other than for safe, secure storage of new fuel

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

    Energy Technology Data Exchange (ETDEWEB)

    Lansard, B

    2004-06-15

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

  1. Plutonium extraction by the formation of insoluble salts (1960); Extraction du plutonium par formation de sels insolubles (1960)

    Energy Technology Data Exchange (ETDEWEB)

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

    1960-06-15

    The aim of this work is to convert Pu IV nitrate in solution into an insoluble salt. Three methods have been studied: 1) the conventional oxalic acid method was improved; 2) precipitation with 8-hydroxyquinoline was tried; 3) the hydrogen peroxide method was adapted to the eluates of the ionic resins from Marcoule. The yield from the oxalic process has been increased (loss of Pu in the mother-liquor brought from 200 mg/l to 20 mg/l). The study of Pu IV precipitation by 8-hydroxyquinoline has shown that the yield is excellent (Pu concentration in the mother-liquor less than 5 mg/h), but decontamination from impurities is nil. Finally, experiments on the precipitation by hydrogen peroxide of Pu IV solutions at the concentrations normally obtained from the anionic resins at Marcoule have given us good yields (Pu concentration in the mother-liquor less than 7 mg/l), and the purification is better than that obtained by oxalic acid (1000 ppm total impurities after a precipitation). (author) [French] L'objet de l'etude est la transformation en sel insoluble du nitrate de Pu IV en solution. Trois procedes ont ete etudies: 1) la methode classique a l'acide oxalique a ete amelioree, 2) la precipitation a la 8-hydroxyquinoleine a ete essayee; 3) le procede a l'eau oxygenee a ete adapte aux solutions d'elution des resines anion de Marcoule. Le rendement du procede oxalique a ete augmente (perte en Pu dans les eaux-meres ramenee de 200 mg/l a 20 mg/l). L'etude de la precipitation du Pu IV par la 8-hydroxyquinoleine a montre que le rendement etait excellent (concentration du Pu dans les eaux-meres inferieure a 5 mg/l), mais la decontamination en impuretes est nulle. Enfin, l'etude et l'application de la precipitation par l'eau oxygenee de solutions de Pu IV de concentrations habituellement obtenues a la sortie des resines anion a Marcoule nous ont permis d'obtenir un bon rendement (concentration de Pu dans les eaux-meres inferieure a 7 mg/l); la purification est meilleure que

  2. 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)

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

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2002-01-01

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

  4. The extraction neptunium by trilaurylamine; L'extraction du neptunium par le trilaurylamine

    Energy Technology Data Exchange (ETDEWEB)

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

    1964-07-01

    The extraction by trilaurylamine of neptunium (IV) from nitric acid and sulfuric acid-nitric acid media has been studied with the aim of developing a purification process for this element. Relative to the plutonium-neptunium separation, conditions are given for the oxidation of neptunium (IV) in sulfuric acid-nitric acid medium and data are presented on the stabilisation of the + 4 oxidation state by the organic solvent. Two procedures have been developed for the simultaneous purification of the two actinides. Both are based on the trilaurylamine extraction of the tetravalent nitrate species. The first utilises a constant redox potential fixed by Fe{sup +++} /Fe{sup ++} couple, while in the second, valencies are determined by successive addition of nitrite and ferrous ions. Gram quantities of neptunium 237 has been recovered from plutonium process solution. Alternate procedures are suggested for the chemical processing of irradiated Np{sup 237}. (authors) [French] L'extraction du neptunium par le trilaurylamine en milieu nitrique et sulfonitrique a ete etudiee dans le cadre de la recherche des procedes de purification de cet element. En vue d'effectuer la separation neptunium-plutonium on a precise d'une part les conditions d'oxydation du Np{sup 4+} en milieu sulfonitrique, d'autre part l'influence du solvant sur la stabilite des valences de ces deux elements. Deux procedes de purification simultanee des deux actinides ont ete developpes. Ils sont bases sur l'extraction du nitrate des elements tetravalents dans la trilaury lamine. Dans l'un, la solution a extraire a un potentiel redox fixe par un systeme auxiliaire (Fe{sup +++}/Fe{sup ++}), dans l'autre elle subit dans le meme extracteur des additions successives de nitrite et de fer ferreux. On decrit un essai semi-industriel de recuperation de neptunium 237 a partir de solution provenant de l'usine de production de plutonium de Marcoule. Differents schemas utilisables lors du traitement chimique des cibles de

  5. A Procedure for the Determination of Alpha-Emitting Plutonium in Urine Using a Solid-State Counter; Methode de Determination du Plutonium Emetteur Alpha Present dans l'Urine, au Moyen d'un Compteur a Semi-Conducteurs; Metod opredeleniya al'fa-izlucheniya plutoniya v moche s pomoshch'yu poluprovodnikovogo schetchika; Procedimiento para Determinar la Actividad Alfa del Plutonio en la Orina con Ayuda de un Contador de Estado Solido

    Energy Technology Data Exchange (ETDEWEB)

    Sandalls, F. J.; Morgan, A. [Health Physics and Medical Division, Atomic Energy Research Establishment, Harwell (United Kingdom)

    1964-10-15

    A method for the routine determination of alpha-emitting plutonium in urine is described. In evolving this procedure various techniques for concentrating, purifying and electro depositing plutonium were compared, and these investigations are summarized. In the procedure finally adopted, urine is wet-ashed and the residue dissolved in hydrochloric acid. Plutonium (IV) is co-precipitated with iron cupferride from this solution and extracted into chloroform. After evaporation of the chloroform, the residue is oxidized, dissolved in hydrochloric acid and the iron extracted into di-isopropyl ether. The aqueous phase containing the plutonium is evaporated and dissolved in an acid ammonium sulphate solution from which the plutonium is electrodeposited onto stainless steel. Quantitative recoveries are obtained over the electrodeposition stage and on overall recovery of 84 {+-} 7%. The electrodeposited plutonium is counted with a solid-state (silicon junction diode) detector in a counter developed for this purpose. The low inherent background of this type of counter is effectively reduced still further by counting only those alpha particles with energy in the 4.2 - 5.4 MeV range. The good resolution which can be obtained with thin electrodeposited sources of plutonium enables this narrow channel to be used with only small losses in counting efficiency. By counting over this restricted energy range, the blank activity arising from reagents and incomplete removal of alpha-emitting contaminants in urine is also reduced by a factor of two, to just over 0.01 pc/24-h sample. The limit of detection with this method is about 0.025 pc of Pu{sup 239}. (author) [French] Les auteurs exposent une methode pour la determination courante du plutonium emetteur alpha present dans l'urine. Pour mettre au point cette methode, ils ont compare diverse procedes de concentration, de purification et de depot electrolytique du plutonium; les resultats de ces recherches sont resumes dans le memoire

  6. Denatured plutonium: a study of deterrent action. Final report

    International Nuclear Information System (INIS)

    Hutchins, B.A.

    1975-07-01

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

  7. Production of Plutonium Metal from Aqueous Solutions

    Energy Technology Data Exchange (ETDEWEB)

    Orth, D.A.

    2003-01-16

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

  8. Biological transfer of plutonium via in vivo labeled goat's milk. Final report

    International Nuclear Information System (INIS)

    Sutton, W.W.; Mullen, A.A.; Lloyd, S.R.; Mosley, R.E.

    1976-03-01

    The long physical and biological half-life and high relative toxicity have dictated that considerable effort be devoted to quantifying plutonium transport through the various trophic levels. Despite the fact that biological transport of plutonium has been studied for many years, quantitative values for its transfer to milk, and its subsequent uptake by suckling animals have not been established. Three lactating goats were given intravenous injections of citrate-buffered plutonium nitrate at a rate of 75 microcuries per animal per day for three consecutive days. In all three goats approximately one percent of the total plutonium dose was transferred to the milk by the fifth post-treatment day. Plutonium retained by the tissues was deposited primarily in the liver and bone. In vitro plutonium-labeled milk was also fed to groups of rats and juvenile goats. Tissue concentrations of plutonium from juvenile goats which had received either in vivo or in vitro labeled milk were somewhat variable. Due possibly to this, within group variability and the small number of animals per group (two) there were no clearly discernible differences between treatments. The only comparison point to show a consistent trend was the observation that, as expected, juvenile rats retained more of the ingested dose than the adult animals

  9. The extraction neptunium by trilaurylamine; L'extraction du neptunium par le trilaurylamine

    Energy Technology Data Exchange (ETDEWEB)

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

    1964-07-01

    The extraction by trilaurylamine of neptunium (IV) from nitric acid and sulfuric acid-nitric acid media has been studied with the aim of developing a purification process for this element. Relative to the plutonium-neptunium separation, conditions are given for the oxidation of neptunium (IV) in sulfuric acid-nitric acid medium and data are presented on the stabilisation of the + 4 oxidation state by the organic solvent. Two procedures have been developed for the simultaneous purification of the two actinides. Both are based on the trilaurylamine extraction of the tetravalent nitrate species. The first utilises a constant redox potential fixed by Fe{sup +++} /Fe{sup ++} couple, while in the second, valencies are determined by successive addition of nitrite and ferrous ions. Gram quantities of neptunium 237 has been recovered from plutonium process solution. Alternate procedures are suggested for the chemical processing of irradiated Np{sup 237}. (authors) [French] L'extraction du neptunium par le trilaurylamine en milieu nitrique et sulfonitrique a ete etudiee dans le cadre de la recherche des procedes de purification de cet element. En vue d'effectuer la separation neptunium-plutonium on a precise d'une part les conditions d'oxydation du Np{sup 4+} en milieu sulfonitrique, d'autre part l'influence du solvant sur la stabilite des valences de ces deux elements. Deux procedes de purification simultanee des deux actinides ont ete developpes. Ils sont bases sur l'extraction du nitrate des elements tetravalents dans la trilaury lamine. Dans l'un, la solution a extraire a un potentiel redox fixe par un systeme auxiliaire (Fe{sup +++}/Fe{sup ++}), dans l'autre elle subit dans le meme extracteur des additions successives de nitrite et de fer ferreux. On decrit un essai semi-industriel de recuperation de neptunium 237 a partir de solution provenant de l'usine de production de plutonium de Marcoule. Differents schemas

  10. 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

  11. Proserpine - plutonium 239 - Proserpine - uranium 235 - comparison of experimental results; Proserpine - plutonium 239 - proserpine - uranium 235 - comparaison de resultats experimentaux

    Energy Technology Data Exchange (ETDEWEB)

    Brunet, J P; Caizergues, R; Clouet D' Orval, Ch; Kremser, J; Moret-Bailly, J; Verriere, Ph [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1964-07-01

    The Proserpine homogeneous reactor is constituted by a tank, 25 cm dia, 30 cm high, surrounded by a composite reflector made of beryllium oxide and graphite. In this tank can be made critical plutonium or 90 per cent enriched uranium solutions, the fissile substances being in the form of a dissolved salt. In varying the concentration of the solution, critical masses were studied as a function of the level of the liquid in the tank. The minimum critical mass is 256 {+-} 2 grs for plutonium and 409 {+-} 3 grs for uranium 235. In the range of the critical concentrations which were studied, the neutronic properties of fissionable solutions of plutonium and enriched uranium were compared for identical geometries. (authors) [French] Proserpine est un reacteur homogene comportant une cuve de diametre 25 cm, de hauteur 30 cm, entouree d'un reflecteur composite d'oxyde de beryllium et de graphite. On y a rendu critiques des solutions de plutonium ou d'uranium enrichi a 90 pour cent, le produit fissile se trouvant sous la forme d'un sel dissous. En faisant varier la concentration de la solution, on a etudie les masses critiques en fonction de la hauteur du liquide dans la cuve. La masse- critique minimum est, pour le plutonium de 256 {+-} 2 g, pour l'uranium 235 de 409 {+-} 3 g. Dans la gamme des concentrations critiques etudiees, on a compare, dans des conditions de geometrie identique, les proprietes neutroniques des solutions fissiles de plutonium et d'uranium enrichi. (auteurs)

  12. Use of tri-laurylamine during the retreatment of irradiated fuels; Utilisation de la trilaurylamine au retraitement des combustibles irradies

    Energy Technology Data Exchange (ETDEWEB)

    Bathellier, A; Koehly, G; Perez, J J; Chesne, A [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1964-07-01

    The purification of aqueous solutions of plutonium can be made by extraction of the Pu (IV) nitrate complex using trilaurylamine in dodecane. The principal physical properties of this solution are considered along with its extractive properties and the influence of foreign ions on the extraction. The application of this method of extraction in a processing cycle for irradiated material is proposed: either for a final purification process or for auxiliary cycles for recovering plutonium from metal production wastes, oxalate precipitation supernatants, or any general aqueous plutonium waste solution. Also proposed are clean-up procedures for regeneration of an extractive solution which has undergone chemical or radiolytic degradation. (authors) [French] La purification du plutonium contenu dans des solutions aqueuses peut etre effectuee par extraction du nitrate de l'ion tetravalent par la trilaurylamine diluee dans du dodecane. Les principales proprietes physiques de ce solvant sont passees en revue ainsi que ses proprietes extractives et l'influence des ions etrangers sur celles-ci. L'application de cette methode d'extraction dans le cycle de traitement des combustibles irradies est envisagee: soit dans le traitement de purification finale, soit dans les cycles annexes ayant trait a la recuperation de plutonium a partir des scories d'elaboration du metal, des eaux-meres oxaliques et d'une facon generale des solutions aqueuses contenant du plutonium. Des traitements de regeneration du solvant ayant subi des degradations chimique ou radiolytique, sont proposes. (auteurs)

  13. Use of tri-laurylamine during the retreatment of irradiated fuels; Utilisation de la trilaurylamine au retraitement des combustibles irradies

    Energy Technology Data Exchange (ETDEWEB)

    Bathellier, A.; Koehly, G.; Perez, J.J.; Chesne, A. [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1964-07-01

    The purification of aqueous solutions of plutonium can be made by extraction of the Pu (IV) nitrate complex using trilaurylamine in dodecane. The principal physical properties of this solution are considered along with its extractive properties and the influence of foreign ions on the extraction. The application of this method of extraction in a processing cycle for irradiated material is proposed: either for a final purification process or for auxiliary cycles for recovering plutonium from metal production wastes, oxalate precipitation supernatants, or any general aqueous plutonium waste solution. Also proposed are clean-up procedures for regeneration of an extractive solution which has undergone chemical or radiolytic degradation. (authors) [French] La purification du plutonium contenu dans des solutions aqueuses peut etre effectuee par extraction du nitrate de l'ion tetravalent par la trilaurylamine diluee dans du dodecane. Les principales proprietes physiques de ce solvant sont passees en revue ainsi que ses proprietes extractives et l'influence des ions etrangers sur celles-ci. L'application de cette methode d'extraction dans le cycle de traitement des combustibles irradies est envisagee: soit dans le traitement de purification finale, soit dans les cycles annexes ayant trait a la recuperation de plutonium a partir des scories d'elaboration du metal, des eaux-meres oxaliques et d'une facon generale des solutions aqueuses contenant du plutonium. Des traitements de regeneration du solvant ayant subi des degradations chimique ou radiolytique, sont proposes. (auteurs)

  14. Stop plutonium; Stop plutonium

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    2003-02-01

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

  15. The testing of a method for dosing plutonium by {alpha}-counting in the presence of strong concentrations of salts or of uranium; Essai d'une methode de dosage du plutonium par comptage {alpha} en presence de fortes concentrations en sels ou en uranium

    Energy Technology Data Exchange (ETDEWEB)

    Fontaine, A M; Baude-Malafosse, L M; Cunq, M J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1961-07-01

    This report describes a method for dosing small quantities of plutonium in a solution having a high concentration of salts. It shows the possibility of dosing up to 5.10{sup -3} {mu}g of Pu in the presence of 10 mg of NaNO{sub 3} with out decreasing the counting-rate. The only error possible is that in the counting. It is also possible to dose 10{sup -3} {mu}g of Pu in the presence of 1,7 mg of uranyl nitrate. (author) [French] Ce rapport decrit une methode de dosage de faibles quantites de plutonium dans une solution de forte concentration en sels. Il montre la possibilite de doser jusqu'a 5.10{sup -3} {mu}g de Pu en presence de 10 mg de NO{sub 3}Na sans diminution du taux de comptage. La seule erreur que l'on puisse faire est l'erreur de comptage. On peut aussi doser 10{sup -3} {mu}g de Pu en presence de 1,7 mg de nitrate d'uranyle. (auteur)

  16. IRSN's opinion on the partial activity resumption for the Plutonium Technology Workshop (ATPu - INB 32) of the Cadarache Centre

    International Nuclear Information System (INIS)

    2009-10-01

    As operations had been suspended for stations where fissile materials were handled in the ATPu (Atelier de Technologie du Plutonium, Plutonium Technology Workshop) of the Cadarache Centre, this document briefly describes the concerned operations (waste treatment and evacuation, glove box dismantling, transfer section dismantling), specifies and comments the measures undertaken by the operator, and gives the IRSN opinion about the resumption of the concerned activities

  17. Effect of the plutonium isotopic composition on the performance of fast reactors; Effet de la composition isotopique du plutonium sur le rendement de reacteurs a neutrons rapides; Vliyanie izotopnogo sostava plutoniya na rabotu reaktorov na bystrykh nejtronakh; Efectos de la composicion isotopica del plutonio sobre el funcionamiento de los reactores rapidos

    Energy Technology Data Exchange (ETDEWEB)

    Yiftah, S [Israel Atomic Energy Commission (Israel)

    1962-03-15

    The isotopic composition of plutonium to be used as fuel for fast reactors will depend on the source of plutonium. In principle three different sources are possible: (a) production reactors; (6) thermal power reactors (using natural uranium or enriched uranium as fuel); (c) fast reactor blankets. In general, source (a) and to some extent source (c) will provide relatively 'clean' plutonium, that is mostly Pu{sup 239}, while plutonium from source (6) will be 'dirty' plutonium, that is plutonium rich in Pu{sup 240}, Pu{sup 241}, and Pu{sup 242}. The degree of 'dirtiness' will depend on the kind of reactor, amount of burn-up and in general on the irradiation history of the fuel. The question then arises, can one use as fuel for fast reactors any kind of plutonium? To investigate the effect of different isotopic composition of the plutonium fuel, in the metallic, oxide and carbide form, on the performance of fast reactors, a limited series of spherical geometry 16-group diffusion theory calculations were performed, using the 16-group cross-section set developed recently by Yiftah, Okrent and Moldauer and taking three different kinds of plutonium, starting with pure Pu{sup 239} and increasing the amount of higher isotopes. For the systems studied-800, 1500 and 2500-l core-volumes, which are typical for large fast power reactors-the result is, when one takes into account only the thermally fissionable isotopes Pu{sup 239} arid Pu{sup 241}, that the 'dirtier' the plutonium, the smaller the critical mass and the higher the breeding ratio. For the 1500-l reactor, taken as an example, it is further found that in the metallic, oxide and carbide plutonium fuels the reactivity change upon removal of 40% of the sodium initially present in the core is made more negative (or less positive) when the plutonium is richer in higher isotopes. (author) [French] La composition isotopique du plutonium qui doit etre utilise comme combustible dans des reacteurs a neutrons rapides depend de

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

    Energy Technology Data Exchange (ETDEWEB)

    1993-05-15

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

  19. Reaction of uranium and plutonium carbides with austenitic steels; Reaction des carbures d'uranium et de plutonium avec des aciers austenitiques

    Energy Technology Data Exchange (ETDEWEB)

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

    1967-07-01

    The reaction of uranium and plutonium carbides with austenitic steels has been studied between 650 and 1050 deg. C using UC, steel and (UPu)C, steel diffusion couples. The steels are of the type CN 18.10 with or without addition of molybdenum. The carbides used are hyper-stoichiometric. Tests were also carried out with UCTi, UCMo, UPuCTi and UPuCMo. Up to 800 deg. C no marked diffusion of carbon into stainless steel is observed. Between 800 and 900 deg. C the carbon produced by the decomposition of the higher carbides diffuses into the steel. Above 900 deg. C, decomposition of the monocarbide occurs according to a reaction which can be written schematically as: (U,PuC) + (Fe,Ni,Cr) {yields} (U,Pu) Fe{sub 2} + Cr{sub 23}C{sub 6}. Above 950 deg. C the behaviour of UPuCMo and that of the titanium (CN 18.12) and nickel (NC 38. 18) steels is observed to be very satisfactory. (author) [French] La reaction des carbures d'uranium et de plutonium avec des aciers austenitiques a ete etudiee entre 650 deg. C et 1050 deg. C a partir de couples de diffusion UC, acier et (UPu)C, acier. Les aciers sont du type CN 18.10 avec ou sans addition de molybdene. Les carbures utilises sont hyper-stoechiometriques. En outre on a fait des essais avec UCTi, UCMo, UPuCTi, UPuCMo. Jusqu'a 800 deg. C on ne detecte pas de diffusion sensible du carbone dans l'acier inoxydable. Entre 800 et 900 deg. C il y a diffusion dans l'acier du carbone provenant de la decomposition des carbures superieurs. A partir de 900 deg. C il y a decomposition du monocarbure selon une reaction que l'on ecrit schematiquement: (U,PuC) + (Fe, Ni, Cr) {yields} (U,Pu)Fe{sub 2} + Cr{sub 23}C{sub 6}. Nous notons a 950 deg. C le bon comportement de UPuCMo ainsi que celui des aciers au titane (CN 18. 12) et au nickel (NC 38.18). (auteur)

  20. Plutonium-239 and americium-241 uptake by plants from soil. Final report

    International Nuclear Information System (INIS)

    Brown, K.W.

    1979-03-01

    Alfalfa was grown in soil contaminated with plutonium-239 dioxide (239PuO2) at a concentration of 29.7 nanocuries per gram (nCi/g). In addition to alfalfa, radishes, wheat, rye, and tomatoes were grown in soils contaminated with americium-241 nitrate (241Am(NO3)3) at a concentration of 189 nCi/g. The length of exposure varied from 52 days for the radishes to 237 days for the alfalfa. The magnitude of plutonium incorporation by the alfalfa as indicated by the concentration ratio, 0.0000025, was similar to previously reported data using other chemical forms of plutonium. The results did indicate, however, that differences in the biological availability of plutonium isotopes do exist. All of the species exposed to americium-241 assimilated and translocated this radioisotope to the stem, leaf, and fruiting structures. The magnitude of incorporation as signified by the concentration ratios varied from 0.00001 for the wheat grass to 0.0152 for the radishes. An increase in the uptake of americium also occurred as a function of time for four of the five plant species. Evidence indicates that the predominant factor in plutonium and americium uptake by plants may involve the chelation of these elements in soils by the action of compounds such as citric acid and/or other similar chelating agents released from plant roots

  1. CONVERSION OF PLUTONIUM TRIFLUORIDE TO PLUTONIUM TETRAFLUORIDE

    Science.gov (United States)

    Fried, S.; Davidson, N.R.

    1957-09-10

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

  2. Diffusion and Kirkendall effect in plutonium-zirconium system; Diffusion et effet Kirkendall dans le systeme plutonium-zirconium

    Energy Technology Data Exchange (ETDEWEB)

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

    1968-10-01

    Results are reported for the chemical diffusion in {epsilon}{beta} phase (bcc) over the range 10 - 70 atomic per cent plutonium. Concentration-penetration curves, obtained by using electron microprobe, have been analysed by Hall and Matano methods. Chemical diffusion coefficients, measured from 650 to 900 deg. C., increase with plutonium concentration and follow the Arrhenius law. Activation energies range from 18000 up to 44000 cal/mole for plutonium concentrations from 60 to 20 atomic per cent plutonium. Kirkendall effect has been observed by the shift of inert markers located originally at the Zr-PuZr interface. Analysis of intrinsic diffusion coefficients variation, flux of the two species and lattice velocity has been carried out by the incremental couples technique by using Darken and Heumann equations. It was found that D{sub Pu} > D{sub Zr}; the ratio D{sub Pu}/D{sub Zr} increases from 1 to 6 over the range 15 - 60 atomic per cent Pu. Activation energies for intrinsic diffusion coefficients vary between 25 and 50 Kcal/mole. (author) [French] Nous donnons des resultats sur la diffusion chimique en phase {epsilon}{beta} (cc) de 10 a 70 pour cent atomique en plutonium. Les courbes concentration-penetration, obtenues par microanalyse X ont ete depouillees par les methodes de HALL et de MATANO. Les coefficients de diffusion chimique mesures de 650 deg. C a 900 deg. C., augmentent avec la concentration en plutonium et suivent la loi d'ARRHENIUS. Les energies d'activation passent de 18000 a 44000 calories par mole pour des concentrations de 60 a 20 pour cent atomique en plutonium. L'existence d'un effet KIRKENDALL a ete mis en evidence par le deplacement de fils inertes places initialement dans le plan de soudure. L'analyse de la variation des coefficients de diffusion intrinseques, des flux des deux especes et de la vitesse du reseau a ete faite par la technique des couples incrementaux en utilisant les equations de DARKEN et de HEUMANN. On trouve D{sub Pu} > D

  3. Safety aspects with regard to plutonium vitrification techniques

    International Nuclear Information System (INIS)

    Gray, L.W.; Kan, T.

    1995-01-01

    Substantial inventories of excess plutonium are expected to result from dismantling US and Russian nuclear weapons. Disposition of this material should be a high priority in both countries. Various disposition options are under consideration. One option is to vitrify the plutonium with the addition of 137 Cs or high-level waste to act as a deterrent to proliferation. The primary safety problem associated with vitrification of plutonium is to avoid criticality in form fabrication and in the final repository over geologic time. Recovery should be as difficult (costly) as the recovery of plutonium from spent fuel

  4. Plutonium Proliferation: The Achilles Heel of Disarmament

    International Nuclear Information System (INIS)

    Leventhal, Paul

    2001-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Gerber, M.S., Fluor Daniel Hanford

    1997-02-18

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

  6. US Department of Energy Plutonium Stabilization and Immobilization Workshop, December 12-14, 1995: Final proceedings

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-05-01

    The purpose of the workshop was to foster communication within the technical community on issues surrounding stabilization and immobilization of the Department`s surplus plutonium and plutonium- contaminated wastes. The workshop`s objectives were to: build a common understanding of the performance, economics and maturity of stabilization and immobilization technologies; provide a system perspective on stabilization and immobilization technology options; and address the technical issues associated with technologies for stabilization and immobilization of surplus plutonium and plutonium- contaminated waste. The papers presented during this workshop have been indexed separately.

  7. Plutonium safety training course

    International Nuclear Information System (INIS)

    Moe, H.J.

    1976-03-01

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

  8. Potentiometric determination of free nitric-acid in trilaurylamine solutions containing plutonium nitrate; Dosage potentiometrique de l'acidite nitrique libre dans les solutions organiques de trilaurylamine

    Energy Technology Data Exchange (ETDEWEB)

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

    1965-07-01

    A potentiometric method of determination of the free nitric acid in trilaurylamine solutions containing plutonium or thorium nitrates is described. The potentiometric titration is carried out in a mixture of benzene and 1,2-dichloro ethane with a standard solution of trilaurylamine as the titrant. When thorium nitrate is present the metal complex is not dissociated then the titration has a single end-point. In the case of plutonium nitrate the partial dissociation of the plutonium complex corresponds to a second point. The experimental error in duplicate analyses of 50 samples is about 1 per cent for free acid concentrations in the range of 0,03 to 0,1 N and plutonium concentrations between 1 to 5 g/l. (authors) [French] Une methode potentiometrique de dosage de l'acidite nitrique libre dans les solutions de trilaurylamine contenant un complexe de plutonium ou de thorium est decrite. La potentiometrie est effectuee en prenant comme base titrante la trilaurylamine et comme milieu de dilution un melange de benzene et de 1,2 dichloroethane. Dans le cas du thorium, le complexe organometallique n'est pas deplace et la courbe de titrage presente un seul point d'inflexion. Dans le cas du plutonium le complexe est partiellement dissocie ce qui correspond a un second saut de potentiel. La moyenne des erreurs experimentales sur 50 echantillons doses a ete d'environ {+-} 1 pour cent sur l'acide libre. Les solutions experimentees contenaient de 0,03 a 0,1 N en acide et de 1 a 5 g/l en plutonium. (auteurs)

  9. Plutonium in nature; Le plutonium dans la nature

    Energy Technology Data Exchange (ETDEWEB)

    Madic, C.

    1994-12-31

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

  10. Constitutional problems in the handling of plutonium

    International Nuclear Information System (INIS)

    Witt, S. de.

    1989-01-01

    Reprocessing and final storage involve two different systems of nuclear energy utilization: with or without the use of plutonium. There is a choice available between these two systems. The paper discusss the constitutional implications of this choice. The permission of the use of plutonium as nuclear fuel by the Atomic Energy Law is irreconcilable with the Basic Law, i.e. the Constitution. If the corresponding provisions of the Atomic Energy Law are repealed, then only the plutonium-related branch will be revoked and not the legal permission of nuclear energy as a whole. The fact is not ignored that the Atomic Energy law does not permit the construction and operation of a plant or the handling of plutonium if this were to violate a basic right. However, the plutonium-related branch of nculear energy utilization inevitably results in such basic right violations; hence the Atomic Energy law is unconstitutional in this respect. (orig./HSCH) [de

  11. Surplus plutonium disposition draft environmental impact statement. Summary

    International Nuclear Information System (INIS)

    1998-07-01

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

  12. 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

  13. Crystallographic study and self irradiation damage on plutonium at low temperature; Etude cristallographique et effets de l'auto-irradiation sur le plutonium a basse temperature

    Energy Technology Data Exchange (ETDEWEB)

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

    1965-05-01

    We have studied the variation of the parameters of {alpha} plutonium and aluminium stabilised {delta} alloys at low temperature, in order to verify the existence of an antiferromagnetic transition at low temperature. The effects of {alpha} particles on the length of a polycrystal of {alpha} plutonium at 4,2 deg. K are also presented at 18 deg. K a plutonium shows no crystallographic change from its structure at room temperature. The thermal expansion coefficients along the 3 axis seem to be positive at this temperature. Therefore a magnetic contribution on thermal expansion coefficients must be small. A dilatation anomaly of {delta}Pu has been observed at 100 deg. K, together with an anomaly of the diffraction lines intensity. No sur-structure line has been observed at 20 deg. K. The length of {alpha} plutonium Increases with time at a rate of about 5 x 10{sup -6} per hour when held in liquid helium. This effect is attributed to the creation of Frenkel pairs. (author) [French] On presente une etude cristallographique a basse temperature du plutonium {alpha} et stabilise {delta} par des additions d'aluminium en vue de verifier l'existence d'une transformation antiferromagnetique a basse temperature. L'effet des particules {alpha} a 4,2 deg. K sur la longueur d'un polycristal de plutonium {alpha} a egalement ete etudie. Il a ete determine que le plutonium {alpha} ne mange pas de phase allotropique Jusqu'a 18 deg. K, les coefficients de dilatation des trois axes de la maille semblent rester positifs. Une eventuelle contribution magnetique sur les coefficients de dilatation devrait donc etre faible. Une legere anomalie de dilatation de Pu {delta} a ete observee a 100 deg. K ainsi qu'une anomalie d'intensite des raies de diffraction. Aucune raie de surstructure n'a ete observee. Le plutonium {alpha} s'allonge lorsqu'il est plonge dans l'helium liquide d'un taux de l'ordre de 5 x 10{sup -6}/heure. Cet effet a ete attribuee a la creation de paires de Frenkel. (auteur)

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

    International Nuclear Information System (INIS)

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

    1995-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

    Garcia, K

    1998-12-31

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

  16. Evaluation of fuel cycle options for plutonium utilization: 1977 study. Final report

    International Nuclear Information System (INIS)

    Pardue, W.M.; Madia, W.J.; Pobereskin, M.; Tripplett, M.B.; Waddell, J.D.

    1977-05-01

    This is the third in a series of three reports on the analysis of plutonium recycle. Analyses are based upon an October, 1976, middle case ERDA forecast of nuclear growth which predicts 510 GWe of nuclear capacity in the year 2000. Four fuel cycle options were reviewed, ranging from no LWR recycle of uranium of plutonium to recycle options both with and without breeder reactors. A special effort was devoted to the review of various estimates of the costs of reprocessing nuclear fuels, with a resulting value of $190/kg of heavy metal (deflated 1975 dollars). The associated range is estimated to $125/kg to $250/kg. Sensitivity analysis of reprocessing costs, uranium consumption, average generation costs, and total discounted costs of electricity indicate that the long-term economic advantages of plutonium recycle are quite conclusive. Nuclear scenarios which project low growth rates and which delay the start of recycle and introduction of a breeder reactor postpone the apparent economic advantages

  17. Plutonium use - Present status and prospects

    International Nuclear Information System (INIS)

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

    1977-01-01

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

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

    International Nuclear Information System (INIS)

    1996-09-01

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

  19. Plutonium working group report on environmental, safety and health vulnerabilities associated with the Department's plutonium storage. Volume II, part 7: Mound working group assessment team report

    International Nuclear Information System (INIS)

    1994-09-01

    This is the report of a visit to the Mound site by the Working Group Assessment Team (WGAT) to assess plutonium vulnerabilities. Purposes of the visit were: to review results of the site's self assessment of current practices for handling and storing plutonium; to conduct an independent assessment of these practices; to reconcile differences and assemble a final list of vulnerabilities; to calculate consequences and probability for each vulnerability; and to issue a report to the Working Group. This report, representing completion of the Mound visit, will be compiled along with those from all other sites with plutonium inventories as part of a final report to the Secretary of Energy

  20. 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)

  1. Plutonium

    International Nuclear Information System (INIS)

    Watson, G.M.

    1976-01-01

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

  2. Pulmonary lesions induced by inhaled plutonium in beagles

    International Nuclear Information System (INIS)

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

    1975-01-01

    The histopathologic features of pulmonary fibrosis and bronchiolo-alveolar carcinoma in beagles exposed to aerosols of plutonium oxide were reviewed. A hypothesis of the pathogenesis of radiation pneumonitis induced by inhalation of plutonium oxide was presented; this hypothesis included phagocytosis of plutonium particles, fibrosis responding to the necrosis, and alveolar cell hyperplasia compensating for alveolar cells killed by alpha radiation. Histopathologic features of the epithelial changes suggest a progression from hyperplasia to metaplasia and, finally, to bronchiolo-alveolar carcinoma. The possibility of concurrent radiation-induced lymphopenia contributing to the development of bronchiolo-alveolar carcinoma through a loss of immunologic surveillance was discussed

  3. An alternative plutonium disposition method

    International Nuclear Information System (INIS)

    Kueppers, C.

    2002-01-01

    This paper provides a feasibility study on vitrification of plutonium with high active waste concentrate, and fabrication of MOX fuel rods for direct final disposal. These are potential alternatives to the direct use of MOX fuel in a reactor. (author)

  4. MIS High-Purity Plutonium Oxide Hydride Product 5501579 (SSR124): Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Veirs, Douglas Kirk [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Stroud, Mary Ann [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Berg, John M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Narlesky, Joshua Edward [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Worl, Laura Ann [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Martinex, Max A. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Carillo, Alex [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2018-02-08

    A high-purity plutonium dioxide material from the Material Identification and Surveillance (MIS) Program inventory has been studied with regard to gas generation and corrosion in a storage environment. Sample 5501579 represents process plutonium oxides from hydride oxide from Rocky Flats that are currently stored in 3013 containers. After calcination to 950°C, the material contained 87.42% plutonium with no major impurities. This study followed over time, the gas pressure of a sample with nominally 0.5 wt% water in a sealed container with an internal volume scaled to 1/500th of the volume of a 3013 container. Gas compositions were measured periodically over a six year period. The maximum observed gas pressure was 124 kPa. The increase over the initial pressure of 70 kPa was primarily due to generation of nitrogen and carbon dioxide gas. Hydrogen and oxygen were minor components of the headspace gas. At the completion of the study, the internal components of the sealed container showed signs of corrosion.

  5. Analysis and composition of the first U-Pu charge (0,043 per cent of Pu); Analyse et constitution du 1. jeu U-Pu (0,043 pour cent de Pu)

    Energy Technology Data Exchange (ETDEWEB)

    Brunet, J P; Lapparent, D de; Lourme, P [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1965-07-01

    Checking the homogeneity in the content of plutonium of 0,043 per cent Pu-natural uranium alloy slugs has been made by Pu 240 and U 238 spontaneous fissions neutrons counting. The purpose of the test was to select groups of slugs to be correctly associated into fuel rods for critical experiments. General technic for spontaneous fissions counting, then elaboration of data in view of ranking the slugs are described. Results are given for this particular case. (authors) [French] On a effectue un controle d'homogeneite de teneur en plutonium sur des billettes d'alliage 0,043 pour cent Pu-uranium naturel, par comptage des fissions spontanees du plutonium 240 et de l'uranium 238. Le but du controle etait de permettre une association correcte de ces billettes a l'interieur des elements combustibles destines a servir dans des experiences critiques. On indique la methode generale de comptage des fissions spontanees, puis le depouillement des donnees en vue du classement des barreaux. Les resultats pour ce cas particulier sont donnes dans le rapport. (auteurs)

  6. Plutonium Finishing Plant. Interim plutonium stabilization engineering study

    Energy Technology Data Exchange (ETDEWEB)

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

    1995-08-01

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

  7. Plutonium Finishing Plant. Interim plutonium stabilization engineering study

    International Nuclear Information System (INIS)

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

    1995-08-01

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

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

    International Nuclear Information System (INIS)

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

    1978-01-01

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

  9. Stop plutonium

    International Nuclear Information System (INIS)

    2003-02-01

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

  10. Quantitative analysis of carbon in plutonium

    International Nuclear Information System (INIS)

    Lefevre, Chantal.

    1979-11-01

    The aim of this study is to develop a method for the determination of carbon traces (20 to 400 ppm) in plutonium. The development of a carbon in plutonium standard is described, then the content of this substance is determined and its validity as a standard shown by analysis in two different ways. In the first method used, reaction of the metal with sulphur and determination of carbon as carbon sulphide, the following parameters were studied: influence of excess reagent, surface growth of samples in contact with sulphur, temperature and reaction time. The results obtained are in agreement with those obtained by the conventional method of carbon determination, combustion in oxygen and measurement of carbon in the form of carbon dioxide. Owing to the presence of this standard we were then able to study the different parameters involved in plutonium combustion so that the reaction can be made complete: temperature reached during combustion, role of flux, metal surface in contact with oxygen and finally method of cleaning plutonium samples [fr

  11. Toxicological profile for plutonium. Final report

    International Nuclear Information System (INIS)

    1990-12-01

    The ATSDR Toxicological Profile for Plutonium is intended to characterize succinctly the toxicological and health effects information for the substance. It identifies and reviews the key literature that describes the substance's toxicological properties. Other literature is presented but described in less detail. The profile is not intended to be an exhaustive document; however, more comprehensive sources of specialty information are referenced. The profile begins with a public health statement, which describes in nontechnical language the substance's relevant toxicological properties. Following the statement is material that presents levels of significant human exposure and, where known, significant health effects. The adequacy of information to determine the substance's health effects is described. Research gaps in nontoxic and health effects information are described. Research gaps that are of significance to the protection of public health will be identified in a separate effort. The focus of the document is on health and toxicological information

  12. Plutonium Finishing Plant safety evaluation report

    International Nuclear Information System (INIS)

    1995-01-01

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

  13. 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

  14. 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

  15. MIS High-Purity Plutonium Oxide Metal Oxidation Product TS707001 (SSR123): Final Report

    Energy Technology Data Exchange (ETDEWEB)

    Veirs, Douglas Kirk [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Stroud, Mary Ann [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Berg, John M. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Narlesky, Joshua Edward [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Worl, Laura Ann [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Martinez, Max A. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Carillo, Alex [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2017-08-09

    A high-purity plutonium dioxide material from the Material Identification and Surveillance (MIS) Program inventory has been studied with regard to gas generation and corrosion in a storage environment. Sample TS707001 represents process plutonium oxides from several metal oxidation operations as well as impure and scrap plutonium from Hanford that are currently stored in 3013 containers. After calcination to 950°C, the material contained 86.98% plutonium with no major impurities. This study followed over time, the gas pressure of a sample with nominally 0.5 wt% water in a sealed container with an internal volume scaled to 1/500th of the volume of a 3013 container. Gas compositions were measured periodically over a six year period. The maximum observed gas pressure was 138 kPa. The increase over the initial pressure of 80 kPa was primarily due to generation of nitrogen and carbon dioxide gas in the first six months. Hydrogen and oxygen were minor components of the headspace gas. At the completion of the study, the internal components of the sealed container showed signs of corrosion, including pitting.

  16. Determination of plutonium in pure plutonium nitrate solutions - Gravimetric method

    International Nuclear Information System (INIS)

    1987-01-01

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

  17. Transmutation of plutonium in pebble bed type high temperature reactors

    International Nuclear Information System (INIS)

    Bende, E.E.

    1997-01-01

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

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

    International Nuclear Information System (INIS)

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

    1975-01-01

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

  19. Harmful effects of DU in the offspring of the military personnel employed in DU contaminated regions

    International Nuclear Information System (INIS)

    Atlagic, N.; Lisov, Lj.; Barjaktarovic, V.; Djurovic, B.; Spasic, Jokic V.

    2008-01-01

    Full text: In 1999, during the NATO attacks on Kosovo, from AT-10 aircraft has been shot over 50000 30-mm projectiles which contained approximately 15 tones of DU. Besides DU, projectiles contained products of DU radioactive decay as well as americium, neptunium, plutonium and technetium. Due to DU contamination military personnel employed near hit targets could be contaminated and irradiated. Besides the harmful effects in exposed military personnel, harmful effects were noticed in their offsprings, too. DU can cause genetic and teratogenic harmful effects in the embryos/fetus. It is concentrated in semen of contaminated males and also can contaminate the embryo/fetus through placenta. DU, as a toxic and radioactive element, can cause variety of harmful effects, but the most important are the effects on DNA which are the cause of many diseases. The aim of this paper is to examine is there any change in the incidence in heritable effects, congenital malformations, malignant diseases, endocrine and immune disorders. For that reason we compared the incidence of these diseases in the offspring's of military personnel born from 1995-1999 (1204) with the children born from 2000-2004 (1131) / and 2005-2008. Our results showed higher incidence of congenital malformations and chromosomal abnormalities (12.55 % vs 4.57 %), with highest incidence of foot deformity-52.04 % and hip deformity. These abnormalities were followed with immunological disorders and dysfunction of the urine bladder. Endocrine diseases were increased too(2.16 % :1.63 %). In this period higher incidence of malignant diseases was not noticed, but in the second period (from 5-9 year) after 1999, higher incidence of malignant hematological diseases was noticed, as well as Down Sy. During the conflicts future parents as well as embryo/fetus are exposed to many harmfulness and it is very hard to separate the influence of each. Considering the fact that the effects of DU, could be delayed and synergistic with

  20. Evaluation of indigenous anion exchange resins for plutonium purification

    International Nuclear Information System (INIS)

    Kumaresan, R.; Sabharwal, K.N.; Srinivasan, T.G.; Vasudeva Rao, P.R.; Thite, B.S.; Ajithlal, R.T.; Sinalkar, Nitin; Dharampurikar, G.R.; Janardhanan, C.; Michael, K.M.; Vijayan, K.; Jambunathan, U.; Dey, P.K.

    2004-01-01

    Preliminary data with pure plutonium nitrate solution indicate that indigenous anion exchange resin can be used for the purification and concentration of plutonium. However, further studies are required to be conducted on larger scale with actual plant feed solutions before arriving to final conclusions. This includes repeated loading and elution cycles studies with the same bed and evaluation of the performance after each cycle

  1. Surplus plutonium disposition draft environmental impact statement. Volume 2

    International Nuclear Information System (INIS)

    1998-07-01

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

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

    International Nuclear Information System (INIS)

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

    1969-01-01

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

  3. Plutonium controversy

    International Nuclear Information System (INIS)

    Gofman, J.W.

    1976-01-01

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

  4. Plutonium in nature

    International Nuclear Information System (INIS)

    Madic, C.

    1994-01-01

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

  5. Recovery of plutonium from lean organic in presence of Ru - activity

    International Nuclear Information System (INIS)

    Govindan, P.; Vijayan, K.S.; Dhamodharan, K.; Sharma, P.K.; Desigan, N.; Mohan, S.V.; Subba Rao, R.V.

    2006-01-01

    Recovery of plutonium from the scrubbed organic by uranous stabilized with hydrazine is carried out. It is observed that the quantitative stripping of plutonium is obtained by a single contact leaving organic with 25.0 mg/L of plutonium containing 0.468mCi/L Ru activity. The retention of plutonium in the lean organic may be attributed to the presence of degradation products and ruthenium activity may be due to the stable complex of ruthenium with TBP. The final strip product almost free from ruthenium is subjected to oxalate precipitation after pre concentration.The proposed method is applied to actual plant stream during reprocessing of high burn up fuel

  6. SEPARATION OF PLUTONIUM

    Science.gov (United States)

    Maddock, A.G.; Smith, F.

    1959-08-25

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

  7. 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.

  8. 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

  9. Non-destructive assay system for uranium and plutonium in reprocessing input solutions. Hybrid K-edge/XRF Densitometer. JASPAS JC-11 final report

    International Nuclear Information System (INIS)

    Surugaya, N.; Abe, K.; Kurosawa, A.; Ikeda, H.; Kuno, Y.

    1997-05-01

    As a part of JASPAS programme, a non-radioactive assay system for the accountability of uranium and plutonium in input dissolver solutions of a spent fuel reprocessing plant, called Hybrid K-edge/XRF Densitometer, has been developed at the Tokai Reprocessing plant (TRP) since 1991. The instrument is the one of the hybrid type combined K-edge densitometry (KED) and X-ray fluorescence (XRF) analysis. The KED is used to determine the uranium concentration and the XRF is used to determine the U/Pu ratio. These results give the plutonium concentration in consequence. It is considered that the instrument has the capability of timely on-site verification for input accountancy. The instrument had been installed in the analytical hot cell at the TRP and the experiments comparing with Isotope Dilution Mass Spectrometry (IDMS) method have been carried out. As the results of measurements for the actual input solutions in the acceptance and performance tests, it was typically confirmed that the precision for determining uranium concentration by the KED was within 0.2%, whereas the XRF for plutonium performed within 0.7%. This final report summarizes the design information and performance data so as to end the JASPAS programme. (author)

  10. Closure Welding of Plutonium Bearing Storage Containers

    International Nuclear Information System (INIS)

    Cannell, G.R.

    2002-01-01

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

  11. The plutonium extraction pilot plant at Chatillon; L'usine-pilote d'extraction du plutonium de Chatillon

    Energy Technology Data Exchange (ETDEWEB)

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

    1958-07-01

    After a brief recapitulation of the problem and its difficulties, the chemical process and the apparatus used are described. The results obtained at the various stages of the separation are then given, as well as the performance by the apparatus. (author) [French] Apres un bref rappel du probleme et de ses difficultes, on decrit le procede chimique et l'appareillage utilises. On donne ensuite les resultats obtenus en ce qui concerne les divers stades de la separation ainsi que les performances fournies par les appareils. (auteur)

  12. International and institutional aspects of reprocessing and plutonium management

    International Nuclear Information System (INIS)

    1978-09-01

    Various institutional alternatives applicable to reprocessing, plutonium management and recycle are considered, not as a definitive analysis but rather as a basis for identifying the institutional approaches and measures which the Working Group might wish to examine more thoroughly. Seven alternatives arrangements for reprocessing are presented. These range from suspending the operation of existing reprocessing plants through placing national facilities under safeguards to limiting reprocessing to a few large facilities subject to plutonium management, multinational or international control. Finally, the comprehensive alternative of an International Nuclear Fuel Authority with worldwide responsibility for reprocessing and plutonium management is considered. Plutonium management alternatives to complement the reprocessing options, are then outlined. These include national discretion on the separation and disposition of plutonium under safeguards, an agreed Code of Practice for plutonium management at national facilities and the international storage of plutonium. The advantages and disadvantages of the alternative are discussed tentatively. It is recognised that the alternatives are presented in a simplified form and that their elements can be combined or separated in many ways. Although strengthening the institutions relating to the peaceful uses of nuclear energy is imperative and can contribute to non-proliferation, such arrangements might open other proliferation risks through the spread of sensitive materials, facilities and technology. While there are risks with any fuel cycle, where plutonium in quantity is separated these risks are of a high order. Although these can be mitigated, they will have to be set against the energy and economic case for reprocessing and alternatives other than plutonium considered

  13. Measurement of Plutonium Isotopic Composition - MGA

    Energy Technology Data Exchange (ETDEWEB)

    Vo, Duc Ta [Los Alamos National Lab. (LANL), Los Alamos, NM (United States)

    2015-08-21

    In this module, we will use the Canberra InSpector-2000 Multichannel Analyzer with a high-purity germanium detector (HPGe) and the MGA isotopic anlysis software to assay a variety of plutonium samples. The module provides an understanding of the MGA method, its attributes and limitations. You will assess the system performance by measuring a range of materials similar to those you may assay in your work. During the final verification exercise, the results from MGA will be combined with the 240Pueff results from neutron coincidence or multiplicity counters so that measurements of the plutonium mass can be compared with the operator-declared (certified) values.

  14. 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)

  15. Recovery of americium-241 from aged plutonium metal

    International Nuclear Information System (INIS)

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

    1980-12-01

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

  16. Life-span studies of inhaled plutonium in beagle dogs

    International Nuclear Information System (INIS)

    Bair, W.J.

    1990-04-01

    In 1970 a life-span study with over 300 beagle dogs was begun to gain an understanding of long-term health effects resulting from respiratory tract intakes of plutonium and to derive risk estimates that might be applied to plutonium and other transuranic elements. Groups of beagle dogs were given single exposures to 239 PuO 2 , 238 PuO 2 , or 239 Pu(NO 3 ) 4 to obtain graded levels of initial lung burdens ranging from 1 to 1800 Bq lung. The objective of this paper is to give you a progress report on the current life-span studies of inhaled plutonium in beagle dogs at the Pacific Northwest Laboratory. I will describe the biokinetics of inhaled plutonium in dogs and the resulting health effects. I will also mention some studies directed towards understanding the mechanism leading to these effects. Finally, I will discuss the current risk estimates derived from these studies and how they might relate to plutonium exposures in humans. 5 refs., 13 figs., 4 tabs

  17. Plutonium

    International Nuclear Information System (INIS)

    Anon.

    1995-01-01

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

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

    International Nuclear Information System (INIS)

    1998-07-01

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

  19. Learning more about plutonium

    International Nuclear Information System (INIS)

    2005-01-01

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

  20. An Appraisal of Analytical Methods for Plutonium and their Applications to the Analysis of Nuclear Materials; Evaluation des Methodes Analytiques de Dosage du Plutonium et de Leur Application a l'Analyse des Matieres Nucleaires; Otsenka analiticheskikh metodov opredeleniya plutoniya i ikh primenenie dlya analiza yadernykh materialov; Metodos Analiticos de Determinacion del Plutonio y su Empleo en el Analisis de Materiales Nucleares

    Energy Technology Data Exchange (ETDEWEB)

    Milner, G. W.C.; Phillips, G. [Atomic Energy Research Establishment, Harwell, Berks. (United Kingdom)

    1966-02-15

    programmes for new nuclear fuels. (author) [French] Il existe plusieurs methodes de dosage de la teneur en plutonium des matieres nucleaires. Pour les quantites de l'ordre du milligramme, les methodes utilisables sont la spectro- photometiie differentielle fondee sur la couleur de Pu (III), la gravimetrie fondee sur PuO{sub 2}, le comptage gamma et les methodes de reduction/oxydation comprenant les titrages poientiometriques et amperemetriques et la coulombmetrie a potentiel constant. Pour les quantites de Tordre du microgramme, le comptage alpha, la dilution isotopique et les methodes polarigraphiques sont a utiliser. Certaines methodes conviennent mieux que d'autres a des types determines d'echantillons et l'analyste soucieux d'obtenir les meilleurs resultats se heurte a un choix difficile. Les auteurs exposent les avantages et les inconvenients des methodes citees tels qu'ils se sont degages de l'experience acquise au cours des annees a l'Atomic Energy Research Establishment, et ils discutent l'exactitude, la precision, la sensibilite de ces methodes, et d'autres caracteristiques presentant un interet particulier. Certaines methodes ne peuvent etre utilisees si l'on n'a, dans une certaine mesure, separe le plutonium des autres constituants de l'echantillon et le memoire commente l'experience acquise avec l'echange d'anions et les procedes de chromatographie a phase inversee utilises a cette fin, en insistant surtout sur la mesure dans laquelle cette methode convient aux echantillons radioactifs. Les auteurs etudient en outre les nombreux problemes qui se sont poses lors de l'application (d'ailleurs couronnee de succes) de ces methodes a l'analyse des alliages de plutonium, des ceramiques et des cermets dans differentes combinaisons contenant de l'uranium, du thorium, du fer, du chrome, du molybdene, du cerium et du cobalt. Us exposent les difficultes de la dissolution des echantillons et de la reduction du plutonium a l'etat de valence voulu, ainsi que les avantages

  1. Safety aspects of Particle Bed Reactor plutonium burner system

    International Nuclear Information System (INIS)

    Powell, J.R.; Ludewig, H.; Todosow, M.

    1993-01-01

    An assessment is made of the safety aspects peculiar to using the Particle Bed Reactor (PBR) as the burner in a plutonium disposal system. It is found that a combination of the graphitic fuel, high power density possible with the PBR and engineered design features results in an attractive concept. The high power density potentially makes it possible to complete the plutonium burning without requiring reprocessing and remanufacturing fuel. This possibility removes two hazardous steps from a plutonium burning complex. Finally, two backup cooling systems depending on thermo-electric converters and heat pipes act as ultimate heat removal sinks in the event of accident scenarios which result in loss of fuel cooling

  2. Criticality experiments with annular cylinders containing plutonium solutions; Experiences de criticite sur des cylindres annulaires contenant des solutions de plutonium

    Energy Technology Data Exchange (ETDEWEB)

    Molbert, M; Sauve, A; Houelle, M; Deilgat, E [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1964-07-01

    slightly with the concentration. On other part, a good agreement was been noticed between those results and the calculations (CEA Report 2488). (authors) [French] La Station de criticite de Dijon dispose de trois cellules, protegees par des murs de beton de 1 m 46 d'epaisseur, servant a abriter les appareillages destines aux experiences de criticite. Le batiment comprend egalement: un atelier de preparation des solutions de plutonium, un laboratoire d'analyses, des stockages de solutions actives, des salles de controle accolees aux cellules. L'une des cellules est occupee par l'appareillage B a l'aide duquel il est prevu d'etudier: des cylindres annulaires, une plaque de 100 mm d'epaisseur et l'interaction de plusieurs recipients cylindriques. Le present rapport groupe les premiers resultats obtenus sur des cylindres annulaires definis par leur geometrie (diametre exterieur et diametre interieur de l'anneau contenant la solution de plutonium). Ces resultats ont ete rassembles sous forme de courbes H{sub c} et M{sub c} = f (c) (ou H{sub c} = hauteur critique, M{sub c} = masse critique et c = concentration en plutonium) pour plusieurs valeurs de la concentration (42,3 g/l < c < 104,1 g/l) et pour diverses conditions de reflexion (reflecteur d'eau interieur et exterieur, ecran de cadmium) et concernent: - des cylindres de 500 x 300; -- cylindre isole -- interaction entre deux cylindres - Dans ce cas particulier les courbes ont ete tracees pour trois concentrations en plutonium, elles donnent H{sub c} et M{sub c} en fonction de la distance entre recipients. - un cylindre de 500 x 200 isole: les resultats publies sont incomplets, les experiences n'etant pas terminees a la date du present rapport. De ces divers resultats ont ete tires les renseignements suivants: - effet d'ecran de l'eau dans la cavite centrale superieure a l'effet de reflexion. Cet effet est accru par une feuille de cadmium plaquee sur la paroi. - des courbes d'interaction 'normalisees' {alpha}*H{sub c}/H{sub c

  3. 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.)

  4. Plutonium behavior during the early diagenesis of marine sediments: applications to two marine environments labelled by radionuclides released from reprocessing plants; Etude du comportement du plutonium au cours de la diagenese precoce des sediments marins: applications a deux environnements marins marques par les rejets issus d'usines de retraitement de combustibles uses

    Energy Technology Data Exchange (ETDEWEB)

    Gouzy, A

    2004-12-15

    The plutonium released into the English Channel and the Irish Sea by nuclear fuel reprocessing plants is mainly associated to sediments. Nevertheless, this association is partially reversible. This work combines a field study, carried out on the Cumbrian mud patch and the Esk estuary (Eastern Irish Sea), and laboratory experiments performed on carbonaceous coarse-grained sediments collected in the Central Channel. It presents new data on the plutonium solid partition in sediments and suggests realistic scenarios for describing its release from sediments to the water column. The role of reactive sulphides acting as temporary sink phases is shown in anoxic sediments; those sulphides are liable to release dissolved plutonium upon their oxidation. The plutonium is also bound to carbonates within the carbonaceous matrix and as carbonate surface complexes. Conceptual schemes of the behaviour of the plutonium in marine sediments are proposed; they highlight the strong remobilization potential of plutonium from marine sediments to the interstitial water. Its plutonium content can be injected into the overlying water column. (author)

  5. Plutonium behavior during the early diagenesis of marine sediments: applications to two marine environments labelled by radionuclides released from reprocessing plants; Etude du comportement du plutonium au cours de la diagenese precoce des sediments marins: applications a deux environnements marins marques par les rejets issus d'usines de retraitement de combustibles uses

    Energy Technology Data Exchange (ETDEWEB)

    Gouzy, A

    2004-12-15

    The plutonium released into the English Channel and the Irish Sea by nuclear fuel reprocessing plants is mainly associated to sediments. Nevertheless, this association is partially reversible. This work combines a field study, carried out on the Cumbrian mud patch and the Esk estuary (Eastern Irish Sea), and laboratory experiments performed on carbonaceous coarse-grained sediments collected in the Central Channel. It presents new data on the plutonium solid partition in sediments and suggests realistic scenarios for describing its release from sediments to the water column. The role of reactive sulphides acting as temporary sink phases is shown in anoxic sediments; those sulphides are liable to release dissolved plutonium upon their oxidation. The plutonium is also bound to carbonates within the carbonaceous matrix and as carbonate surface complexes. Conceptual schemes of the behaviour of the plutonium in marine sediments are proposed; they highlight the strong remobilization potential of plutonium from marine sediments to the interstitial water. Its plutonium content can be injected into the overlying water column. (author)

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1961-07-01

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

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

    International Nuclear Information System (INIS)

    1998-07-01

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

  8. 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

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

    International Nuclear Information System (INIS)

    Forsberg, C.W.

    1995-01-01

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

  10. 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

    occurs only if they are physically proximal in solution or the plutonium present in the solid phase is intimately mixed with compounds or solutions of these absorbers. No information on the potential chemical interaction of plutonium with cadmium was found in the technical literature. Definitive evidence of sorption or adsorption of plutonium onto various solid phases from strongly alkaline media is less clear-cut, perhaps owing to fewer studies and to some well-attributed tests run under conditions exceeding the very low solubility of plutonium. The several studies that are well-founded show that only about half of the plutonium is adsorbed from waste solutions onto sludge solid phases. The organic complexants found in many Hanford tank waste solutions seem to decrease plutonium uptake onto solids. A number of studies show plutonium sorbs effectively onto sodium titanate. Finally, this report presents findings describing the behavior of plutonium vis-à-vis other elements during sludge dissolution in nitric acid based on Hanford tank waste experience gained by lab-scale tests, chemical and radiochemical sample characterization, and full-scale processing in preparation for strontium-90 recovery from PUREX sludges.

  11. Simultaneous determination of plutonium and uranium in environmental samples

    International Nuclear Information System (INIS)

    Jiao Shufen

    1993-01-01

    Plutonium and uranium in a plant sample ash was simultaneously determined by using anion exchange resin columns, and concentrated hydrochloric acid and nitric acid. At the final stage of the determination of the nuclides, each of them was electrodeposited together with a little amount of molybdenum carrier onto a stainless steel plate and measured by α-ray spectrometer. The recoveries of uranium and plutonium from the plant samples determined by adding internal standard 236 Pu which was 100% and 63%, respectively

  12. Plutonium solubilities

    International Nuclear Information System (INIS)

    Puigdomnech, I.; Bruno, J.

    1991-02-01

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

  13. 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

  14. Conversion of metal plutonium to plutonium dioxide by pyrochemical method

    Energy Technology Data Exchange (ETDEWEB)

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

    2000-07-01

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

  15. The use of plutonium

    International Nuclear Information System (INIS)

    Marshall, W.

    1980-01-01

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

  16. Properties of plutonium

    International Nuclear Information System (INIS)

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

    1996-03-01

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

  17. Properties of plutonium

    Energy Technology Data Exchange (ETDEWEB)

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

    1996-03-01

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

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

    International Nuclear Information System (INIS)

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

    1985-01-01

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

  19. High-temperature enthalpies of plutonium monocarbide and plutonium sesquicarbide

    International Nuclear Information System (INIS)

    Oetting, F.L.

    1979-01-01

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

  20. Skeletal lesions from inhaled plutonium in beagles

    International Nuclear Information System (INIS)

    Dagle, G.E.; Park, J.F.; Weller, R.E.; Ragan, H.A.; McClanahan, B.J.; Fisher, D.R.

    1984-10-01

    The report briefly reviews the skeletal effects observed in ongoing lifespan studies in beagle dogs at 13, 10, and 7 years, respectively, after inhalation exposure to 239 Pu oxide and nitrate or 238 Pu oxide. Plutonium nitrate was chosen to represent soluble material more readily translocated to bone and other tissues than the oxide. Bone lesions related to plutonium exposure were observed only in dogs exposed to 238 Pu oxide and 239 Pu nitrate. The skeleton accumulated approximately 2% ( 239 Pu oxide), 45% ( 238 Pu oxide) or 50% ( 239 Pu nitrate) of the final body burdens at 13, 10, and 7 years, respectively, after exposure. 11 references, 2 figures

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1988-05-01

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

  2. Guidelines for the responsible management of plutonium

    International Nuclear Information System (INIS)

    Agrell, P.H.

    1997-01-01

    Since 1994 an informal group of representatives of States party to the NPT has been trying to develop agreed international guidelines for the responsible management of non-military plutonium. This paper gives a brief description of the outcome. Since the results are still subject to decision by Governments, the description must be in general terms only. The paper describes the background to, and genesis of, the discussions and the general approach taken, which was based on commitment to the NPT, national responsibility for the management of nuclear materials and the fuel cycle, upholding of the IAEA's safeguards system, and a focus on civil material. An indication is given of the development of the Group's thinking, especially the decisions that any guidelines must be capable of accommodating surplus military plutonium, as well as civil, and that the main focus should be on measures to increase transparency. The resulting guidelines are described. Their main features are a re-statement of commitments and standards for the management of non-military plutonium with regard to non-proliferation, safety, and other fields, a commitment to the management of such plutonium according to a consistent national strategy, and a commitment to the publication of information on that strategy, and of annual statistics for holdings of plutonium in a consistent format. Other aspects of the guidelines are also explained. Finally, an attempt is made to assess the possible practical effects of the guidelines if adopted by governments. (author)

  3. Plutonium

    International Nuclear Information System (INIS)

    Koelzer, W.

    1989-03-01

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

  4. Laboratory directed research and development on disposal of plutonium recovered from weapons. FY1994 final report

    International Nuclear Information System (INIS)

    Pitts, J.H.; Choi, J.S.

    1994-01-01

    This research project was conceived as a multi-year plan to study the use of mixed plutonium oxide-uranium oxide (MOX) fuel in existing nuclear reactors. Four areas of investigation were originally proposed: (1) study reactor physics including evaluation of control rod worth and power distribution during normal operation and transients; (2) evaluate accidents focusing upon the reduced control rod worth and reduced physical properties of PuO 2 ; (3) assess the safeguards required during fabrication and use of plutonium bearing fuel assemblies; and (4) study public acceptance issues associated with using material recovered from weapons to fuel a nuclear reactor. First year accomplishments are described. Appendices contain 2 reports entitled: development and validation of advanced computational capability for MOX fueled ALWR assembly designs; and long-term criticality safety concerns associated with weapons plutonium disposition

  5. Plutonium

    International Nuclear Information System (INIS)

    Mueller-Christiansen, K.; Wollesen, M.

    1979-01-01

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

  6. Studies and manufacture of plutonium fuel

    International Nuclear Information System (INIS)

    Bussy, P.; Mustelier, J.P.; Pascard, R.

    1964-01-01

    The studies carried out at the C.E.A. on the properties of fast neutron reactor fuels, the manufacture of fuel elements and their behaviour under irradiation are broadly outlined. The metal fuels studied are the ternary alloys U Pu Mo, U Pu Nb, U Pa Ti, U Pa Zr, the ceramic fuels being mixed uranium and plutonium oxides, carbides and nitrides obtained by sintering. Results are given on the manufacture of uranium fuel elements containing a small proportion of plutonium, used in a critical experiment, and on the first experiments in the manufacture of fuel elements for the reactor Rapsodie. Finally the results of irradiation tests carried out on the prototype fuel pins for Rapsodie are described. (authors) [fr

  7. 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.

  8. Plutonium storage phenomenology

    International Nuclear Information System (INIS)

    Szempruch, R.

    1995-12-01

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

  9. Plutonium controversy

    International Nuclear Information System (INIS)

    Richmond, C.R.

    1980-01-01

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

  10. Plutonium ocean shipment safety between Europe and Japan

    International Nuclear Information System (INIS)

    Pierce, J.D.; Hohnstreiter, G.F.; McClure, J.D.; Smith, J.D.; Dukart, R.J.; Koski, J.A.; Braithwate, J.W.; Sorenson, N.R.; Yamamoto, K.; Kitamura, T.; Shibata, K.; Ouchi, Y.; Ito, T.

    2004-01-01

    Sandia National Laboratories (SNL) and Japan Nuclear Cycle Development Institute (JNC) have conducted an extensive emergency response planning study of the safety of the sea transport of plutonium for JNC. This study was conducted in response to international concerns about the safety of the marine transport of PuO2 powder that began with the sea transport of plutonium powder from France to Japan in 1992 using a purposebuilt ship. This emergency response planning study addressed four topics to better define the accident environment for long-range sea transport of nuclear materials. The first topic is a probabilistic safety analysis that evaluates the technical issues of transporting plutonium between Europe and Japan. An engine-room fire aboard a purposebuilt ship is evaluated as the second topic to determine the vulnerability and safety margin of radioactive material packaging for plutonium designed to meet International Atomic Energy Agency (IAEA) standards. The third topic is a corrosion study performed for generic plutonium packaging to estimate the time required to breach the containment boundary in the event of submersion in seawater. The final study topic is a worldwide survey of information on high-value cargo salvage capabilities from sunken ships. The primary purpose of this overall emergency response planning study is to describe and analyze the safety of radioactive material transportation operations for the international transportation of radioactive materials by maritime cargo vessels

  11. Plutonium ocean shipment safety between Europe and Japan

    Energy Technology Data Exchange (ETDEWEB)

    Pierce, J D; Hohnstreiter, G F; McClure, J D; Smith, J D; Dukart, R J; Koski, J A; Braithwate, J W; Sorenson, N R [Sandia National Labs., Albuquerque, NM (United States); Yamamoto, K; Kitamura, T; Shibata, K; Ouchi, Y; Ito, T [Japan Nuclear Cycle Development Inst., Tokai-mura (Japan)

    2004-07-01

    Sandia National Laboratories (SNL) and Japan Nuclear Cycle Development Institute (JNC) have conducted an extensive emergency response planning study of the safety of the sea transport of plutonium for JNC. This study was conducted in response to international concerns about the safety of the marine transport of PuO2 powder that began with the sea transport of plutonium powder from France to Japan in 1992 using a purposebuilt ship. This emergency response planning study addressed four topics to better define the accident environment for long-range sea transport of nuclear materials. The first topic is a probabilistic safety analysis that evaluates the technical issues of transporting plutonium between Europe and Japan. An engine-room fire aboard a purposebuilt ship is evaluated as the second topic to determine the vulnerability and safety margin of radioactive material packaging for plutonium designed to meet International Atomic Energy Agency (IAEA) standards. The third topic is a corrosion study performed for generic plutonium packaging to estimate the time required to breach the containment boundary in the event of submersion in seawater. The final study topic is a worldwide survey of information on high-value cargo salvage capabilities from sunken ships. The primary purpose of this overall emergency response planning study is to describe and analyze the safety of radioactive material transportation operations for the international transportation of radioactive materials by maritime cargo vessels.

  12. Critical experiments in AQUILON with fuels slightly enriched in uranium 235 or in plutonium; Experiences critiques dans aquilon portant sur des combustibles legerement enrichis en uranium 235 et en plutonium

    Energy Technology Data Exchange (ETDEWEB)

    Chabrillac, M; Ledanois, G; Lourme, P; Naudet, R [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1964-07-01

    Reactivity comparisons have been, made in Aquilon II between geometrically identical lattices differing only by the composition of the fuel. The fuel elements consist in metallic uranium single rods with either slight differences of the isotopic composition (0.69 - 0.71 - 0.83 - 0.86 per cent of uranium 235) or slight additions of plutonium (0.043 per cent). Five lattices pitches have bean used, in order to produce a large variation of spectrum. Two additional sets of plutonium fuels are prepared to be used in the same conditions. The double comparisons: natural enriched 235 versus natural-enriched plutonium are made in such a way that a very precise interpretation is permitted. The results are perfectly consistent which seems to prove that the calculation methods are convenient. Further it can been inferred that the usual data, namely for the ratio of the {eta} of {sup 235}U and {sup 239}Pu seem reliable. (authors) [French] On a compare neutroniquement dans Aquilon II des reseaux geometriquement identiques mais comportant de petites differences de composition du combustible. EL s'agit de barres d'uranium metallique, les unes avec des teneurs differentes en isotopes 235 (0,69 - 0,71 - 0,83 - 0,86 pour cent) les autres comportant une legere addition de plutonium (0,043 pour cent). Les comparaisons ont ete faites a cinq pas differents, de maniere a mettre en jeu une assez large variation de spectre. Deux autres jeux de combustible au plutonium seront utilises ulterieurement dans les memes conditions. Les resultats des mesures se presentent sous forme de doubles comparaisons: naturel-enrichi 235/naturel-enrichi plutonium. On s'est place dans des conditions qui permettent des interpretations tres precises. Les resultats sont remarquablement coherents, ce qui semble montrer que les methodes de calcul sont bien adaptees, Ils tendent d'autre part a prouver que les valeurs numeriques admises dans la litterature, notamment pour le rapport des {eta} de l'U 235 et de Pu 239

  13. Perspective on plutonium

    International Nuclear Information System (INIS)

    Sun, L.S.

    1993-01-01

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

  14. Geochemistry of uranium and thorium series nuclides and of plutonium in the Gulf of Mexico: Final report

    International Nuclear Information System (INIS)

    Scott, M.R.

    1986-01-01

    This project focussed on the question of the transport of plutonium by the Mississippi River and the subsequent fate of that material when it entered the ocean. Samples were collected from the Mississippi and its tributaries, and from other rivers spanning a gradation in climate from the arid Rio Grande region to the subtropical Suwannee River. Plutonium analyses of water and of suspended and bottom sediments were complemented with Fe, Mn, Al, CaCO 3 , and organic matter measurements. Analyses of uranium and thorium isotopes, 210 Pb, and 226 Ra were made to serve both as tracers for transport processes, and (for the reactive nuclides) as steady state chemical analogues for plutonium

  15. Plutonium controversy

    Energy Technology Data Exchange (ETDEWEB)

    Richmond, C.R.

    1980-01-01

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

  16. The plutonium as transfer tracer and particulates contribution accumulating from the Rhone to the north-western Mediterranean sea; Le plutonium comme traceur du transfert et de l`accumulation des apports particulaires du Rhone en Mediterranee nord-occidentale

    Energy Technology Data Exchange (ETDEWEB)

    Noel, M.H.

    1996-03-29

    To follow the alluvial deposits from the Rhone in Mediterranean Sea, since the principle hydroelectric constructions (1960), it was necessary to find an adequate tracer. The plutonium isotopes have satisfied to the different characteristics. The specificity of the Rhone contribution is bound to the existence of the irradiated spent fuels reprocessing plant of Marcoule; the releases of this plant are characterized by the predominance of Plutonium 238. The results of this study show that the percentage of sediments coming from the Rhone in the recent contribution, is low beyond the pro delta: less than 5% of the sediment of the continental shelf concern the Rhone contribution. However, there are two zones for which the contribution is important and could play a role in the particulate transfer towards the high sea. (N.C.). 157 refs., 60 figs., 50 tabs.

  17. 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

  18. Crystalline matrices for the immobilization of plutonium and actinides

    Energy Technology Data Exchange (ETDEWEB)

    Anderson, E.B.; Burakov, E.E.; Galkin, Ya.B.; Starchenko, V.A.; Vasiliev, V.G. [V.G. Khlopin Radium Institute, St. Petersburg (Russian Federation)

    1996-05-01

    The management of weapon plutonium, disengaged as a result of conversion, is considered together with the problem of the actinide fraction of long-lived high level radioactive wastes. It is proposed to use polymineral ceramics based on crystalline host-phases: zircon ZrSiO{sub 4} and zirconium dioxide ZrO{sub 2}, for various variants of the management of plutonium and actinides (including the purposes of long-term safe storage or final disposal from the human activity sphere). It is shown that plutonium and actinides are able to form with these phases on ZrSiO{sub 4} and ZrO{sub 2} was done on laboratory level by the hot pressing method, using the plasmochemical calcination technology. To incorporate simulators of plutonium into the structure of ZrSiO{sub 4} and ZrO{sub 2} in the course of synthesis, an original method developed by the authors as a result of studying the high-uranium zircon (Zr,U) SiO{sub 4} form Chernobyl {open_quotes}lavas{close_quotes} was used.

  19. Effects of inhaled plutonium nitrate on bone and liver in dogs

    International Nuclear Information System (INIS)

    Dagle, G.E.; Weller, R.E.; Watson, C.R.; Buschbom, R.L.

    1994-04-01

    The life-span biological effects of inhaled soluble, alpha-emitting radionuclides deposited in the skeleton and liver were studied in 5 groups of 20 beagles exposed to initial lung depositions ranging from 0.48 to 518 Bq/g of lung. Average plutonium amounts in the lungs decreased to approximately 1% of the final body deposition in dogs surviving 5 years or more; more than 90% of the final depositions accumulated in the liver and skeleton. The liver-to-skeletal ratio of deposited plutonium was 0.83. The incidence of bone tumors, primarily osteogenic sarcomas causing early mortality, at final group average skeletal depositions of 15.8, 2.1, and 0.5 Bq/g was, respectively, 85%, 50%, and 5%; there were no bone tumors in exposure groups with mean average depositions lower than 0.5 Bq/g. Elevated serum liver enzyme levels were observed in exposure groups down to 1.3 Bq/g. The incidence of liver tumors at final group average liver depositions of 6.9, 1.3, 0.2, and 0.1 Bq/g, was, respectively, 25%, 15%, 15%, and 15%; one hepatoma occurred among 40 control dogs. The risk of the liver cancer produced by inhaled plutonium nitrate was difficult to assess due to the competing risks of life shortening from lung and bone tumors

  20. Plutonium storage criteria

    Energy Technology Data Exchange (ETDEWEB)

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

    1996-05-01

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

  1. Toxicology of plutonium

    International Nuclear Information System (INIS)

    Bair, W.J.

    1974-01-01

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

  2. Industrial treatment of solutions of fission products. Separation of caesium-137; Traitement industriel de solutions de produits de fission. Separation du cesium-137

    Energy Technology Data Exchange (ETDEWEB)

    Fisher, C; Raggenbass, A [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

    1959-07-01

    Two types of chemical treatment can be considered for the manufacture of solid sources for industrial uses from fission product solutions remaining after plutonium extraction: a) concentration of the solution and preparation of solid sources from the bulk material, without separation, b) separation of one or several fission products from which the sources are made. Examination of the radio-chemical composition of the mixture of fission products that will be available from the Marcoule reactors (G1, G2 and G3) shows that caesium-137 accounts for 30 per cent of the {gamma} energy available immediately after the plutonium separation, 70 per cent two years after and 100 per cent after five years. There is practically no advantage in making sources from bulk fission products, since the separation of caesium-137 is no more complicated and yet it results in a material with more potential uses. The separation of caesium-137 by a method based on the standard phospho-tungstate precipitation method has been considered. Previously, the precipitated caesium phospho-tungstate was dissolved and caesium was recovered from the solution by cation-exchange or by removal of phosphate and tungstate ions by anion-exchange. A study has now been made, of the metathesis of caesium phospho-tungstate to barium phosphate and tungstate by the action of barium hydroxide, the caesium being obtained in solution as the hydroxide. The advantages of this new procedure are: - greater decontamination of caesium-137 without further purification, - possibility of direct transformation to caesium sulphate, - general simplification of the procedure and, consequently, of the equipment. (author) [French] Deux types de traitement chimique peuvent etre envisages pour amener a l'etat de sources solides utilisables industriellement les produits de fission contenus dans les solutions residuaires de l'extraction du plutonium. Ces traitements sont les suivants: a) concentration des solutions et confection de

  3. Industrial treatment of solutions of fission products. Separation of caesium-137; Traitement industriel de solutions de produits de fission. Separation du cesium-137

    Energy Technology Data Exchange (ETDEWEB)

    Fisher, C.; Raggenbass, A. [Commissariat a l' Energie Atomique, Saclay (France).Centre d' Etudes Nucleaires

    1959-07-01

    Two types of chemical treatment can be considered for the manufacture of solid sources for industrial uses from fission product solutions remaining after plutonium extraction: a) concentration of the solution and preparation of solid sources from the bulk material, without separation, b) separation of one or several fission products from which the sources are made. Examination of the radio-chemical composition of the mixture of fission products that will be available from the Marcoule reactors (G1, G2 and G3) shows that caesium-137 accounts for 30 per cent of the {gamma} energy available immediately after the plutonium separation, 70 per cent two years after and 100 per cent after five years. There is practically no advantage in making sources from bulk fission products, since the separation of caesium-137 is no more complicated and yet it results in a material with more potential uses. The separation of caesium-137 by a method based on the standard phospho-tungstate precipitation method has been considered. Previously, the precipitated caesium phospho-tungstate was dissolved and caesium was recovered from the solution by cation-exchange or by removal of phosphate and tungstate ions by anion-exchange. A study has now been made, of the metathesis of caesium phospho-tungstate to barium phosphate and tungstate by the action of barium hydroxide, the caesium being obtained in solution as the hydroxide. The advantages of this new procedure are: - greater decontamination of caesium-137 without further purification, - possibility of direct transformation to caesium sulphate, - general simplification of the procedure and, consequently, of the equipment. (author) [French] Deux types de traitement chimique peuvent etre envisages pour amener a l'etat de sources solides utilisables industriellement les produits de fission contenus dans les solutions residuaires de l'extraction du plutonium. Ces traitements sont les suivants: a) concentration des solutions et

  4. A rapid and specific titrimetric method for the precise determination of plutonium using redox indicator

    International Nuclear Information System (INIS)

    Chitnis, R.T.; Dubey, S.C.

    1976-01-01

    A simple and rapid method for the determination of plutonium in plutonium nitrate solution and its application to the purex process solutions is discussed. The method involves the oxidation of plutonium to Pu(VI) with the help of argentic oxide followed by the destruction of the excess argentic oxide by means of sulphamic acid. The determination of plutonium is completed by adding ferrous ammonium sulphate solution which reduces Pu(VI) to Pu(IV) and titrating the excess ferrous with standard potassium dichromate solution using sodium diphenylamine sulphonate as the internal indicator. The effect of the various reagents add during the oxidation and reduction of plutonium, on the final titration has been investigated. The method works satisfactorily for the analysis of plutonium in the range of 0.5 to 5 mg. The precision of the method is found to be within 0.1%. (author)

  5. Chemical species of plutonium in Hanford radioactive tank waste

    International Nuclear Information System (INIS)

    Barney, G.S.

    1997-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-03-15

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

  7. The role of troublesome components in plutonium vitrification

    Energy Technology Data Exchange (ETDEWEB)

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

    1996-05-01

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

  8. Plutonium re-cycle in HTR

    Energy Technology Data Exchange (ETDEWEB)

    Desoisa, J. A.

    1974-03-15

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

  9. Final generic environmental statement on the routine use of plutonium-powered cardiac pacemakers. Update of information on power sources for pacemakers

    International Nuclear Information System (INIS)

    1979-05-01

    The Final Environmental Statement on Routine Use of Plutonium-Powered Cardiac Pacemakers (FES) was issued in July 1976. Supplement 1, prepared in 1978, updates the FES with respect to power sources for pacemakers. Particular attention is given to the non-nuclear lithium batteries as alternatives to 238-Pu power sources in pacemakers. Supplement 1 also considers the current extent of pacemaker use and makeup of the patient population and concludes that the FES' conclusion is still valid that distribution of 238-Pu powered pacemakers for routine use should be authorized subject to specific conditions

  10. PLUTONIUM-ZIRCONIUM ALLOYS

    Science.gov (United States)

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

    1960-08-30

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

  11. Integrated development and testing plan for the plutonium immobilization project

    International Nuclear Information System (INIS)

    Kan, T.

    1998-01-01

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

  12. Optimization and plutonium equilibrium

    International Nuclear Information System (INIS)

    Silver, G.L.

    1976-01-01

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

  13. 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)

  14. 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

  15. 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.

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

    International Nuclear Information System (INIS)

    Gutierrez Martinez, E.A.

    1998-02-01

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

  17. High-temperature vacuum distillation separation of plutonium waste salts

    International Nuclear Information System (INIS)

    Garcia, E.

    1996-01-01

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

  18. Plutonium working group report on environmental, safety and health vulnerabilities associated with the department's plutonium storage. Volume II, part 11: Lawrence Berkeley Laboratory working group assessment team report

    International Nuclear Information System (INIS)

    1994-09-01

    President Clinton has directed an Interagency Working Group to initiate a comprehensive review of long-term options for the disposition of surplus plutonium. As part of this initiative, Secretary of Energy, Hazel O'Leary, has directed that a Department of Energy project be initiated to develop options and recommendations for the safe storage of these materials in the interim. A step in the process is a plutonium vulnerability assessment of facilities throughout the Department. The Plutonium Vulnerability Working Group was formed to produce the Project and Assessment Plans, to manage the assessments and to produce a final report for the Secretary by September 30, 1994. The plans established the approach and methodology for the assessment. The Project Plan specifies a Working Group Assessment Team (WGAT) to examine each of the twelve DOE sites with significant holdings of plutonium. The Assessment Plan describes the methodology that the Site Assessment Team (SAT) used to report on the plutonium holdings for each specific site.This report provides results of the assessment of the Lawrence Berkeley Laboratory

  19. Plutonium roundtable discussion

    International Nuclear Information System (INIS)

    Penneman, R.A.

    1982-01-01

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

  20. Protection of personnel against atmospheric contamination by plutonium in the laboratory (1963); Protection du personnel contre la contamination atmospherique par le plutonium, dans les laboratoires (1963)

    Energy Technology Data Exchange (ETDEWEB)

    Feliers, P; Pomarola, J; Risselin, A [Commissariat a l' Energie Atomique, Fontenay-aux-Roses (France). Centre d' Etudes Nucleaires

    1963-07-01

    Various problems about measurement of atmospheric contamination by plutonium in laboratories are considered. In particular are studied sampling methods, continuous measurement for alarm, criteria used for fixation of the concentrations to be measured, sensitivity of apparatus and effects of natural atmospheric contamination. The means actually available for measurement of contamination and their limits of use are briefly analysed. (authors) [French] Les differents problemes a resoudre pour realiser un controle satisfaisant de la contamination atmospherique par le plutonium, dans les laboratoires, sont abordes. On etudie en particulier les differents modes d'echantillonnage, le controle continu en vue de l'alarme, les criteres qui servent a la fixation des concentrations a mesurer, la sensibilite a donner aux moyens de mesure, les difficultes provenant de la contamination atmospherique naturelle. Les moyens actuellement disponibles pour le controle de la contamination et leurs moyens limites d'emploi sont analyses sommairement. (auteurs)

  1. Disposition of excess weapon grade plutonium: Status of the Russian program

    Energy Technology Data Exchange (ETDEWEB)

    Diyakov, Anatoly [Center for Arms Control, Energy and Environmental Studies, Moscow (Russian Federation)

    2015-07-01

    During the Cold War, the Soviet Union and United States produced huge quantities of plutonium for weapons. Substantial cuts in their nuclear arsenals released of huge amounts of weapon grade nuclear materials. This put into the agenda the problem what to do with the excess weapon materials. In 2000 Russia and the United States concluded a Plutonium Management and Disposition Agreement (PMDA), committing each to eliminate 34 tons of excess weapon plutonium. It was expected that the implementation of the PMDA Agreement will start in the second half of the year 2009 and the disposition programs finalized in 2025. But from the very beginning the practical implementation of the PMDA agreement met with substantial difficulties. After the consultations held in 2006-2007 the PMDA Agreement was modified. In compliance with the modified Agreement each side pledged to start the disposition of 34 tons of excess plutonium (25 tons in the form of metal and 9 tons in dioxide) in 2018 and to finalize the process in 15 years. Both sides were supposed to use the same disposition method through use in the MOX fuel and its subsequent irradiation in civil nuclear reactors: in light reactors for the USA and in fast neutron reactors for Russia. The presentation is going to provide the current status of the disposition program.

  2. 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

  3. F. Biological hazards of plutonium

    International Nuclear Information System (INIS)

    1976-01-01

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

  4. DOE plutonium disposition study: Analysis of existing ABB-CE Light Water Reactors for the disposition of weapons-grade plutonium. Final report

    Energy Technology Data Exchange (ETDEWEB)

    1994-06-01

    Core reactivity and basic fuel management calculations were conducted on the selected reactors (with emphasis on the System 80 units as being the most desirable choice). Methods used were identical to those reported in the Evolutionary Reactor Report. From these calculations, the basic mission capability was assessed. The selected reactors were studied for modification, such as the addition of control rod nozzles to increase rod worth, and internals and control system modifications that might also be needed. Other system modifications studied included the use of enriched boric acid as soluble poison, and examination of the fuel pool capacities. The basic geometry and mechanical characteristics, materials and fabrication techniques of the fuel assemblies for the selected existing reactors are the same as for System 80+. There will be some differences in plutonium loading, according to the ability of the reactors to load MOX fuel. These differences are not expected to affect licensability or EPA requirements. Therefore, the fuel technology and fuel qualification sections provided in the Evolutionary Reactor Report apply to the existing reactors. An additional factor, in that the existing reactor availability presupposes the use of that reactor for the irradiation of Lead Test Assemblies, is discussed. The reactor operating and facility licenses for the operating plants were reviewed. Licensing strategies for each selected reactor were identified. The spent fuel pool for the selected reactors (Palo Verde) was reviewed for capacity and upgrade requirements. Reactor waste streams were identified and assessed in comparison to uranium fuel operations. Cost assessments and schedules for converting to plutonium disposition were estimated for some of the major modification items. Economic factors (incremental costs associated with using weapons plutonium) were listed and where possible under the scope of work, estimates were made.

  5. Use of plutonium for power production

    International Nuclear Information System (INIS)

    1965-01-01

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

  6. World status report: plutonium

    International Nuclear Information System (INIS)

    Dircks, W.

    1992-01-01

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

  7. Plutonium working group report on environmental, safety and health vulnerabilities associated with the department's plutonium storage. Volume II, part 10: Sandia National Laboratories - New Mexico working group assessment team report

    International Nuclear Information System (INIS)

    1994-09-01

    The Secretary of Energy's memorandum of March 15, 1994, established an initiative for a Department-wide assessment of the vulnerabilities of the inventory of plutonium in storage. Plutonium in intact nuclear weapons and spent fuel were excluded from this study. The DOE Plutonium Vulnerability Working Group, which was formed for this purpose and produced the Project and Assessment Plans, will also manage the open-quote snap-shot close-quote assessments and produce a final report for the Secretary by September 30, 1994. The Project Plan and Assessment Plan to accomplish this study, and which established responsibilities for personnel essential to the study, were issued on April 25, 1994

  8. 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

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

    Energy Technology Data Exchange (ETDEWEB)

    Nishimura, D T

    1957-11-15

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

  10. Determination of plutonium in environment

    International Nuclear Information System (INIS)

    Sakanoue, Masanobu

    1978-01-01

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

  11. Multi-generational stewardship of plutonium

    International Nuclear Information System (INIS)

    Pillay, K.K.S.

    1997-01-01

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

  12. The disposition of weapon grade plutonium: costs and tradeoffs

    International Nuclear Information System (INIS)

    Weida, W.J.

    1996-01-01

    This paper explores some of the economic issues surrounding a major area of expenditures now facing the nuclear powers: the disposition of weapon-grade plutonium either through 'burning' in nuclear reactors for power generation or by other means. Under the current budgeting philosophy in the United States, programs managed by the Department of Energy (DOE) tend to compete with one another for the total funds assigned to that agency. For example, in the FY1995 DOE budget a tradeoff was made between increased funding for nuclear weapons and reduced funding for site cleanup. No matter which disposition alternative is chosen, if disposition funds are controlled by the DOE in the US or by a government agency in any other country, disposition is likely to compete directly or indirectly with other alternatives for energy funding. And if they are subsidized by any government, research into plutonium as reactor fuel or the operations associated with such use are likely to consume funds that might otherwise be available to support sustainable energy alternatives. When all costs are considered, final waste disposal costs will be incurred whatever disposal option is taken. These costs could potentially be offset by doing something profitable with the plutonium prior to final storage, but this paper has shown that finding a profitable use for plutonium is unlikely. Thus, the more probable case is one where the costs of basic waste storage are increased by whatever costs are associated with the disposition option chosen. The factors most likely to significantly increase costs appear to arise from four areas: (1) The level of subsidization in the 'profitable' parts of the disposition program. (2) Those items (such as reprocessing) that increase the volume of waste and thus, the cost of waste disposal. (3) The cost of security and its direct relationship to the number of times plutonium is handled or moved. (4) The cost of research and development of new and unproven methods of

  13. Plutonium in the marine environment

    International Nuclear Information System (INIS)

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

    1994-01-01

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

  14. Plutonium retention in dairy calves following ingestion of either in vivo labeled or in vitro labeled milk

    International Nuclear Information System (INIS)

    Sutton, W.W.; Patzer, R.G.; Hahn, P.B.; Potter, G.D.

    1977-01-01

    Holstein calves, 4 to 8 days of age, were used to compare the gastrointestinal uptake of plutonium-238 from either in vivo or in vitro plutonium-labeled milk. In vivo labeled milk was collected from intravenously dosed lactating adults and the in vitro labeled milk was prepared at the same nuclide concentration by adding citrate-buffered plutonium nitrate to uncontaminated cow's milk. Dosing was accomplished with individual plastic feeding buckets twice daily for 7 consecutive days. The calves were sacrificed 2 days after the final plutonium dose, at which time tissues were collected for nuclide analysis

  15. Radiolysis of aqueous solution of plutonium; Radiolyse des solutions aqueuses de plutonium

    Energy Technology Data Exchange (ETDEWEB)

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

    1960-07-01

    reduction of IV into III was measured with HClO{sub 4}. (author) [French] On a etudie l'action des rayons gamma sur les solutions aqueuses de plutonium a divers etats de valence, en milieu sulfurique, perchlorique, nitrique et chlorhydrique. Le phenomene principal est la reduction de Pu VI en Pu V suivie de la dismutation de la valence V en VI et IV. Pour les solutions d'acide sulfurique et perchlorique 0,2N on a donne le mecanisme des reactions: la radiolyse de l'eau conduit aux produits OH, H{sub 2}O{sub 2}, H et H{sub 2}. Pu VI est reduit par H and H{sub 2}O{sub 2} tandis que Pu V est reoxyde par OH. Cependant l'action de l'eau oxygenee est lente et provoque un effet prolonge. Une etude menee parallelement sur l'action de H{sub 2}O{sub 2} a confirme ceci. Les mesures de disparition de Pu VI et d'apparition de Pu IV faites par spectrophotometrie ont conduit a determiner G{sub H{sub 2}}{sub O{sub 2}} = 0,8 et G{sub H} - G{sub OH} = 0,8. Par microanalyse de gaz on a mesure G{sub H{sub 2}} = 0,41. Ces donnees permettent de calculer le rendement de radiolyse de l'eau G{sub {sup -}}{sub H{sub 2}}{sub O} = 4,35. Les ions sulfate ont une influence complexe sur la reoxydation de Pu V comme le montrent les resultats obtenus sur des solutions plus concentrees en H{sub 2}SO{sub 4}. La reduction se poursuit jusqu'a la valence Ill en milieu perchlorique. Les ions Cl{sup -} et surtout NO{sub 3}{sup -} inhibent la reduction et peuvent la supprimer completement. L'action des particules {alpha} du plutonium et du polonium est tres analogue a celle de l'eau oxygenee. La reduction a lieu apres des periodes d'induction plus ou moins longues selon l'anion (surtout HSO{sub 4}{sup -} ). Elles sont liees a l'accumulation de H{sub 2}O{sub 2} et (ou) de peroxyde de plutonium. Aux faibles acidites le peroxyde de Pu IV a tendance a conduire a des formes polymerisees. Dans les cas les plus simples (H{sub 2}SO{sub 4} et HClO{sub 4} 0,2N) les rendements suivants ont ete obtenus ou calcules: G

  16. Plutonium Training Opportunities

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-03-26

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

  17. Optimizing Plutonium stock management

    International Nuclear Information System (INIS)

    Niquil, Y.; Guillot, J.

    1997-01-01

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

  18. Safeguardability of the vitrification option for disposal of plutonium

    Energy Technology Data Exchange (ETDEWEB)

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

    1996-05-01

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

  19. Final generic environmental statement on the use of recycle plutonium in mixed oxide fuel in light water cooled reactors. Volume 3

    International Nuclear Information System (INIS)

    1976-08-01

    An assessment is presented of the health, safety and environmental effects of the entire light water reactor fuel cycle, considering the comparative effects of three major alternatives: no recycle, recycle of uranium only, and recycle of both uranium and plutonium. The assessment covers the period from 1975 through the year 2000 and includes the cumulative effects for the entire period as well as projections for specific years. Topics discussed include: the light water reactor with plutonium recycle; mixed oxide fuel fabrication; reprocessing plant operations; supporting uranium fuel cycle; transportation of radioactive materials; radioactive waste management; storage of plutonium; radiological health assessment; extended spent fuel storage; and blending of plutonium and uranium at reprocessing plants

  20. Dosimetric optimization approach for activities of metal plutonium elaboration by calciothermy; Demarche d'optimisation dosimetrique des activites d'elaboration du plutonium metal par calciothermie

    Energy Technology Data Exchange (ETDEWEB)

    Crovisier, Ph.; Brunetti, L.; Jourde, S.; Piot, J.; Valier Brasier, P. [CEA/DAMNA/DSTA - Service de Protection contre les Rayonnements- Centre de Valduc - 21120 Is sur Tille (France)

    2008-07-01

    The authors present the activities performed within a new unit of a plutonium pyro-chemistry laboratory, report a dosimetric assessment of workstation in this unit, compare the data with those obtained with the previous installation, and report a study of the neutronic efficiency of biological protection shields (measurements of neutron spectra)

  1. Ceramification: A plutonium immobilization process

    Energy Technology Data Exchange (ETDEWEB)

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

    1996-05-01

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

  2. Treatment of plutonium contaminations

    International Nuclear Information System (INIS)

    Lafuma, J.

    1983-01-01

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

  3. Modelling the transport of sediments and plutonium from the Mururoa lagoon

    International Nuclear Information System (INIS)

    Rajar, R.; Zagar, D.

    1999-01-01

    The paper deals with the three-dimensional simulation of resuspension and transport of sediments from the Mururoa lagoon into the Pacific Ocean. These sediments were contaminated mainly by plutonium during French nuclear tests (from 1966 to 1996). Two cases were simulated: 'Normal conditions', taking into account permanent action of trade winds and tides and 'storm conditions', where the effect of a tropical cyclone with maximum wind velocity of 150 km/h and with a frequency of 1 storm per 10 years is simulated. The final results show, that the normal conditions cause an annual outflow of 8 x 10 4 tons of sediment and 8 GBq of plutonium, while one tropical cyclone would cause outflow of 3.9 x 10 6 tons of sediment and about 0.7 TBq of plutonium. (author)

  4. Fabrication of mixed oxide fuel using plutonium from dismantled weapons

    International Nuclear Information System (INIS)

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

    1996-01-01

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

  5. Plutonium isotopes in the environment

    International Nuclear Information System (INIS)

    Holm, E.

    1977-12-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1958-07-01

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

  7. Plutonium oxides and uranium and plutonium mixed oxides. Carbon determination

    International Nuclear Information System (INIS)

    Anon.

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

  8. Cigarette smoke and plutonium

    International Nuclear Information System (INIS)

    Filipy, R.E.

    1985-01-01

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

  9. Final report on special impact tests of plutonium shipping containers description of test results

    International Nuclear Information System (INIS)

    Bonzon, L.L.

    1977-02-01

    The results from tests conducted to determine the structural response of the LLD-1, Model 1518-6M, and FL-10 plutonium shipping packages when subjected to high-speed impacts (170 to 760 ft/sec) onto unyielding, concrete, and soil targets are presented

  10. HB-Line Plutonium Oxide Data Collection Strategy

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-05-26

    identifies the required facility procedures, DCS print outs, and laboratory results needed to assemble a final data package for each HB-Line plutonium oxide interim oxide can. The data traveler may identify the specific values (data) required to be extracted from the collected facility procedures and DCS print outs. The data traveler may also identify associated criteria to be checked. Inevitably there will be procedure anomalies during the course of the HB-Line plutonium oxide campaign that will have to be addressed in a timely manner.

  11. Hazards of plutonium and fuel reprocessing

    International Nuclear Information System (INIS)

    Watson, G.M.

    1978-01-01

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

  12. Plutonium spectrophotometric analysis

    International Nuclear Information System (INIS)

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

    1990-01-01

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

  13. Plutonium safe handling

    International Nuclear Information System (INIS)

    Tvehlov, Yu.

    2000-01-01

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

  14. Survey of the chemical diffusion at infinite dilution in the nickel-plutonium and aluminium-uranium systems; Contribution a l'etude de l'heterodiffusion a dilution infinie systemes nickel-plutonium et aluminium-uranium

    Energy Technology Data Exchange (ETDEWEB)

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

    1968-09-01

    Solubility S{sub 0} and chemical diffusion coefficients D{sub PuNi} at infinite dilution of plutonium in nickel have been determined by autoradiography {alpha} in poly-phased system by the welded couples method: S{sub 0} varies from 40 to 80.10{sup -6} (atomic concentration) and D{sub PuNi} follows an Arrhenius law D = D{sub 0} exp (-Q/RT) with 0.03 cm{sup 2}/s < D{sub 0} < 1.6 cm{sup 2}/s and 46000 cal/mole < Q < 56000 cal/mole. Diffusion of uranium in aluminium have been carried out by fissiography using the thin layer method. Frequency factor lies between 0.01 and 3.1 cm{sup 2}/s and the activation energy lies between 24000 and 34000 cal/mole. (author) [French] La solubilite S{sub 0} et les coefficients de diffusion chimique D{sub PuNi}, a dilution infinie, du plutonium dans le nickel ont ete determines par autoradiographie {alpha} sur des couples soudes en systeme polyphase. Entre 1000 et 1125 deg. C. S{sub 0} varie de 40 a 80.10{sup -6} et D obeit a une loi d'ARRHENIUS (concentration atomique) D = D{sub 0} exp (-Q/RT) avec 0.03 cm{sup 2}s{sup -1} < D{sub 0} < 1.60 cm{sup 2}s{sup -1} 46000 calories par mole < Q < 56000 calories par mole. La diffusion de l'uranium dans l'aluminium a ete etudiee par fissiographie en utilisant la technique du depot mince. Le facteur de frequence est situe entre 0.01 et 3.1 cm{sup 2}s{sup -1} et l'energie d'activation entre 24000 et 34000 calories par mole. (auteur)

  15. Burning weapons-grade plutonium in reactors

    International Nuclear Information System (INIS)

    Newman, D.F.

    1993-06-01

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

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

    International Nuclear Information System (INIS)

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

    1983-01-01

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

  17. METHOD OF PRODUCING PLUTONIUM TETRAFLUORIDE

    Science.gov (United States)

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

    1959-12-15

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

  18. 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

  19. Design of an ion exchange column for plutonium recovery

    International Nuclear Information System (INIS)

    Araujo, J.A. de; Matsuda, H.T.; Santos Tome Lobao, A. dos; Quesada, A.C.

    1994-01-01

    An ion exchange column design for plutonium recovering from scraps of the MOX fuel elements fabrication is presented. The proposed column is constructed in 304 stainless steel and borosilicate glass provided of heating-jacket and temperature control and pressure relief devices. Safety aspects required for alpha emitters handling have been also considered. The design and construction were performed totally at Brazilian Institute for Energetic and Nuclear Research. The equipment will be used in the plutonium separation step as a part of an installation named Facilidad Alfa at the Centro Atomico de Constituyentes-CNEA/Buenos Aires, where other processes, including dissolution denitration by microwaves and final steps of MOX pellets re-fabrication will be performed. (author). 4 refs, 3 figs

  20. Plutonium Plant, Trombay

    International Nuclear Information System (INIS)

    Yadav, J.S.; Agarwal, K.

    2017-01-01

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

  1. The toxicity of plutonium

    International Nuclear Information System (INIS)

    Crouse, P.L.

    1994-01-01

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

  2. Plutonium use in foreign countries (03)

    International Nuclear Information System (INIS)

    Otagaki, Takao

    2004-03-01

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

  3. Cigarette smoke and plutonium

    International Nuclear Information System (INIS)

    Filipy, R.E.

    1983-01-01

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

  4. Cycle downstream: the plutonium question

    International Nuclear Information System (INIS)

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

    1998-01-01

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

  5. Aqueous Solution Chemistry of Plutonium

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-01-28

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

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

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  7. Speciation of the plutonium at trace levels by capillary electrophoresis-ICP-MS coupling

    International Nuclear Information System (INIS)

    Ambard, Ch.

    2007-01-01

    The CE-ICP-MS coupling allowed the development of new analytical methods for the study of plutonium speciation at trace levels including complexation studies of this element by organic and inorganic ligands. First, a method, called dual detection, based on the simultaneous use of the UV-Visible spectrophotometer integrated in the capillary electrophoresis and the ICPMS was developed and validated. It allows the unambiguous determination of electrophoretic mobilities for separated chemical species and gives a powerful tool for speciation studies. Then, the influence on plutonium redox speciation of the buffer from the background electrolyte was evaluated. This study showed the implications of the electrolyte constituents' choice on plutonium redox equilibrium in the sample. Furthermore, the CE-ICP-MS coupling was used for studying the plutonium complexation at trace levels by some organic (NTA and DTPA) and inorganic ligands (carbonates). The behaviour of plutonium valence +III, +IV and +VI was studied in the presence of buffer at near neutral pH. Different species of plutonium were observed depending on the initial oxidation state of the plutonium. This study showed the potential of poly-amino-carboxylic acids, such as NTA and DTPA, for dissolving plutonium precipitates, regardless its initial speciation. Finally, the carbonation of pentavalent neptunium, as an analogue of Pu(V), was achieved at very low concentration of Np (10 -8 mol.L -1 ). The formation constant of NpO 2 (CO 3 )- at 25 deg. C and 2,5 x 10 -2 mol.L -1 ionic strength was measured by CE-ICP-MS and found to be consistent with literature data. (author)

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

    International Nuclear Information System (INIS)

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

    1979-01-01

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

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

    International Nuclear Information System (INIS)

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

    2011-01-01

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

  10. Plutonium stabilization and disposition focus area, FY 1999 and FY 2000 multi-year program plan

    International Nuclear Information System (INIS)

    1998-03-01

    Consistent with the Environmental Management's (EM's) plan titled, ''Accelerating Cleanup: Paths to Closure'', and ongoing efforts within the Executive Branch and Congress, this Multi-Year Program Plan (MYPP) for the Plutonium Focus Area was written to ensure that technical gap projects are effectively managed and measured. The Plutonium Focus Area (PFA) defines and manages technology development programs that contribute to the effective stabilization of nuclear materials and their subsequent safe storage and final disposition. The scope of PFA activities includes the complete spectrum of plutonium materials, special isotopes, and other fissile materials. The PFA enables solutions to site-specific and complex-wide technology issues associated with plutonium remediation, stabilization, and preparation for disposition. The report describes the current technical activities, namely: Plutonium stabilization (9 studies); Highly enriched uranium stabilization (2 studies); Russian collaboration program (2 studies); Packaging and storage technologies (6 studies); and PFA management work package/product line (3 studies). Budget information for FY 1999 and FY 2000 is provided

  11. Plutonium stabilization and disposition focus area, FY 1999 and FY 2000 multi-year program plan

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-03-01

    Consistent with the Environmental Management`s (EM`s) plan titled, ``Accelerating Cleanup: Paths to Closure``, and ongoing efforts within the Executive Branch and Congress, this Multi-Year Program Plan (MYPP) for the Plutonium Focus Area was written to ensure that technical gap projects are effectively managed and measured. The Plutonium Focus Area (PFA) defines and manages technology development programs that contribute to the effective stabilization of nuclear materials and their subsequent safe storage and final disposition. The scope of PFA activities includes the complete spectrum of plutonium materials, special isotopes, and other fissile materials. The PFA enables solutions to site-specific and complex-wide technology issues associated with plutonium remediation, stabilization, and preparation for disposition. The report describes the current technical activities, namely: Plutonium stabilization (9 studies); Highly enriched uranium stabilization (2 studies); Russian collaboration program (2 studies); Packaging and storage technologies (6 studies); and PFA management work package/product line (3 studies). Budget information for FY 1999 and FY 2000 is provided.

  12. Recovery of plutonium by pyroredox processing

    International Nuclear Information System (INIS)

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

    1985-09-01

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

  13. Recovery of plutonium by pyroredox processing

    International Nuclear Information System (INIS)

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

    1985-01-01

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

  14. The use of calorimetry for plutonium assay

    International Nuclear Information System (INIS)

    Mason, J.A.

    1982-12-01

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

  15. Weapons-grade plutonium dispositioning. Volume 4

    International Nuclear Information System (INIS)

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

    1993-06-01

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

  16. The Macdonald and Savage titrimetric procedure scaled down to 4 mg sized plutonium samples. P. 1

    International Nuclear Information System (INIS)

    Kuvik, V.; Lecouteux, C.; Doubek, N.; Ronesch, K.; Jammet, G.; Bagliano, G.; Deron, S.

    1992-01-01

    The original Macdonald and Savage amperometric method scaled down to milligram-sized plutonium samples was further modified. The electro-chemical process of each redox step and the end-point of the final titration were monitored potentiometrically. The method is designed to determine 4 mg of plutonium dissolved in nitric acid solution. It is suitable for the direct determination of plutonium in non-irradiated fuel with a uranium-to-plutonium ratio of up to 30. The precision and accuracy are ca. 0.05-0.1% (relative standard deviation). Although the procedure is very selective, the following species interfere: vanadyl(IV) and vanadate (almost quantitatively), neptunium (one electron exchange per mole), nitrites, fluorosilicates (milligram amounts yield a slight bias) and iodates. (author). 15 refs.; 8 figs.; 7 tabs

  17. D and D of a plutonium research laboratory and related auxiliary systems

    International Nuclear Information System (INIS)

    Diaz Arocas, P.; Martinez Ortega, A.; Sama Colao, J.; Garcia Diaz, A.; Torre Rodriguez, J.; Diaz Diaz, J.L.; Argiles, E.; Garrido, C.

    2010-01-01

    CIEMAT, former Junta de Energia Nuclear (JEN) started nuclear research at the 60. decade, focussed on the development of pacific uses of Nuclear Energy. At that time, CIEMAT research and pilot plants developed involved the whole nuclear fuel cycle steps. It means from the uranium recovery to the spent fuel reprocessing. With this scope a plutonium research laboratory was constructed and operated from 1961 to the 90's focussed on chemistry of plutonium studies, separation processes and radiochemical analyses, in order to assist the working pilot plants at the Centre. Thereafter, as the result of the changes on the research objectives of CIEMAT, the plutonium laboratory suffered several modifications and finally it was safety stopped due to the obsolescence of its equipments and auxiliary systems. Present paper shows the D and D activities performed and techniques developed to avoid alpha emitter contamination. In every dismantling phase there were established the measures of operational radiological protection adapted to the radiological risk. Dosimetric controls realized during dismantlement showed that incorporation of radionuclides was not detected. Radiological final control was performed applying the derived levels of declassification to request the installation decommissioning. (authors)

  18. Recovery studies for plutonium machining oil coolant

    International Nuclear Information System (INIS)

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

    1977-01-01

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

  19. A review of the properties of plutonium, its biological effects, and its place in the nuclear fuel cycle

    International Nuclear Information System (INIS)

    Harte, G.A.

    1978-03-01

    After a brief description of the sources of plutonium and its physical, chemical and radioactive characteristics, an attempt is made to describe quantitatively the biological effects of plutonium intake as they are currently understood by the organisations concerned with radiological protection. The conceptual basis of protection standards as put forward by ICRP has recently undergone a change; the idea of limiting dose to a critical organ has been superseded by that of limiting the overall risk of carcinogenic and genetic effects. Limits on plutonium intake are discussed in the light of both concepts. Finally the role of plutonium in the nuclear fuel cycle is described. (author)

  20. Plutonium use in foreign countries (01)

    International Nuclear Information System (INIS)

    Otagaki, Takao

    2002-03-01

    European countries and Japan had been implementing the strategy of spent fuel reprocessing in order to use nuclear material to the maximum. Plutonium recovered from reprocessing, however, must be recycle on light water reactors (LWRs) because of considerable delay of fast reactor development. In Europe, much of experience of plutonium recycling have been accumulated until now. Thus, the status of plutonium recycling up to the end of 2001 in France, Germany, The U.K., Belgium, Switzerland and other countries were studied based on the following scope. (1) Basic policy and present status of plutonium recycling in primary countries of France, Germany, The U.K., Belgium, Switzerland, and Sweden which recently appears the move of recycling a part of plutonium. Backend policy and the status of spent fuel management were studied, then integrated analysis and evaluation of the position of plutonium recycling in backend and the status of plutonium recycling development were performed. (2) Plan and experience of Mixed Oxide (MOX) fuel fabrication and reprocessing of spent fuels. The data and information on plan and experience of MOX fuel fabrication and reprocessing in foreign countries were collected. (3) Plutonium inventories. The data and information on plutonium inventories of foreign countries were collected. (author)

  1. Plutonium use in foreign countries (99)

    International Nuclear Information System (INIS)

    Otagaki, Takao

    2000-03-01

    European countries and Japan had been implementing the strategy of spent fuel reprocessing in order to use nuclear material to the maximum. Plutonium recovered from reprocessing, however, must be recycle on light water reactors (LWRs) because of considerable delay of fast reactor development. In Europe, much of experience of plutonium recycling have been accumulated until now. Thus, the status of plutonium recycling up to the end of 1999 in France, Germany, The U.K., Belgium, Switzerland and other countries were studied based on the following scope. (1) Basic policy and present status of plutonium recycling in primary countries of France, Germany, The U.K., Belgium, Switzerland, and Sweden which recently appears the move to recycling a part of plutonium backend policy and the status of spent fuel management were studied, then integrated analysis and evaluation of the position of plutonium recycling in backend and the status of plutonium recycling development were performed. (2) Plan and experience of Mixed Oxide (MOX) fuel fabrication and reprocessing of spent fuels. The data and information on plan and experience of MOX fuel fabrication and reprocessing in foreign countries were collected. (3) Plutonium inventories. The data and information on plutonium inventories of foreign counties were collected. (author)

  2. Plutonium use in foreign countries (02)

    International Nuclear Information System (INIS)

    Otagaki, Takao

    2003-02-01

    European countries and Japan had been implementing the strategy of spent fuel reprocessing in order to use nuclear material to the maximum. Plutonium recovered from reprocessing, however, must be recycle on light water reactors (LWRs) because of considerable delay of fast reactor development. In Europe, much of experience of plutonium recycling have been accumulated until now. Thus, the status of plutonium recycling up to the end of 2002 in France, Germany, The U.K., Belgium, Switzerland and other countries were studied based on the following scope. (1) Basic policy and present status of plutonium recycling in primary countries of France, Germany, The U.K., Belgium, Switzerland, and Sweden which recently appears the move of recycling a part of plutonium. Backend policy and the status of spent fuel management were studied, then integrated analysis and evaluation of the position of plutonium recycling in backend and the status of plutonium recycling development were performed. (2) Plan and experience of Mixed Oside (MOX) fuel fabrication and reprocessing of spent fuels. The data and information on plan and experience of MOX fuel fabrication and reprocessing in foreign countries were collected. (3) Plutonium inventories. The data and information on plutonium inventories of foreign countries were collected. (author)

  3. Plutonium use in foreign countries. (04)

    International Nuclear Information System (INIS)

    Otagaki, Takao

    2005-03-01

    European countries and Japan had been implementing the strategy of spent fuel reprocessing in order to use nuclear material to the maximum. Plutonium recovered from reprocessing, however, must be recycle on light water reactors (LWRs) because of considerable delay of fast reactor development. In Europe, much of experience of plutonium recycling have been accumulated until now. Thus, the status of plutonium recycling up to the end of 2004 in France, Germany, The U.K., Belgium, Switzerland and other countries were studied based on the following scope. (1) Basic policy and present status of plutonium recycling in primary countries of France, Germany, the U.K., Belgium, Switzerland, and Sweden which plans to recycle a limited amount of plutonium: Backend policy and the status of spent fuel management were studied, then integrated analysis and evaluation of the position of plutonium recycling in backend and the status of plutonium recycling development were performed. (2) Plan and experience of Mixed Oxide (MOX) fuel fabrication and reprocessing of spent fuels: The data and information on plan and experience of MOX fuel fabrication and reprocessing in foreign countries were collected. (3) Plutonium inventories: The data and information on plutonium inventories of foreign countries were collected. (author)

  4. Laboratory-scale evaluations of alternative plutonium precipitation methods

    International Nuclear Information System (INIS)

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

    1984-01-01

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

  5. The plutonium danger

    International Nuclear Information System (INIS)

    Ruiter, W. de

    1983-01-01

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

  6. Measurement and instrumentation techniques for monitoring plutonium and uranium particulates released from nuclear facilities

    International Nuclear Information System (INIS)

    Nero, A.V. Jr.

    1976-08-01

    The purpose of this work has been an analysis and evaluation of the state-of-the-art of measurement and instrumentation techniques for monitoring plutonium and uranium particulates released from nuclear facilities. The occurrence of plutonium and uranium in the nuclear fuel cycle, the corresponding potential for releases, associated radiological protection standards and monitoring objectives are discussed. Techniques for monitoring via decay radiation from plutonium and uranium isotopes are presented in detail, emphasizing air monitoring, but also including soil sampling and survey methods. Additionally, activation and mass measurement techniques are discussed. The availability and prevalence of these various techniques are summarized. Finally, possible improvements in monitoring capabilities due to alterations in instrumentation, data analysis, or programs are presented

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

    International Nuclear Information System (INIS)

    Sampath, S.; Chawla, K.L.

    1975-01-01

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

  8. The plutonium challenge for the future

    International Nuclear Information System (INIS)

    Gray, L.W.

    2000-01-01

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

  9. Annealing of (DU-10Mo)-Zr Co-Rolled Foils

    International Nuclear Information System (INIS)

    Pacheco, Robin Montoya; Alexander, David John; Mccabe, Rodney James; Clarke, Kester Diederik; Scott, Jeffrey E.; Montalvo, Joel Dwayne; Papin, Pallas; Ansell, George S.

    2017-01-01

    Producing uranium-10wt% molybdenum (DU-10Mo) foils to clad with Al first requires initial bonding of the DU-10Mo foil to zirconium (Zr) by hot rolling, followed by cold rolling to final thickness. Rolling often produces wavy (DU-10Mo)-Zr foils that should be flattened before further processing, as any distortions could affect the final alignment and bonding of the Al cladding to the Zr co-rolled surface layer; this bonding is achieved by a hot isostatic pressing (HIP) process. Distortions in the (DU-10Mo)-Zr foil may cause the fuel foil to press against the Al cladding and thus create thinner or thicker areas in the Al cladding layer during the HIP cycle. Post machining is difficult and risky at this stage in the process since there is a chance of hitting the DU-10Mo. Therefore, it is very important to establish a process to flatten and remove any waviness. This study was conducted to determine if a simple annealing treatment could flatten wavy foils. Using the same starting material (i.e. DU-10Mo coupons of the same thickness), five different levels of hot rolling and cold rolling, combined with five different annealing treatments, were performed to determine the effect of these processing variables on flatness, bonding of layers, annealing response, microstructure, and hardness. The same final thickness was reached in all cases. Micrographs, textures, and hardness measurements were obtained for the various processing combinations. Based on these results, it was concluded that annealing at 650°C or higher is an effective treatment to appreciably reduce foil waviness.

  10. Annealing of (DU-10Mo)-Zr Co-Rolled Foils

    Energy Technology Data Exchange (ETDEWEB)

    Pacheco, Robin Montoya [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Alexander, David John [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Mccabe, Rodney James [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Clarke, Kester Diederik [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Scott, Jeffrey E. [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Montalvo, Joel Dwayne [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Papin, Pallas [Los Alamos National Lab. (LANL), Los Alamos, NM (United States); Ansell, George S. [Colorado School of Mines, Golden, CO (United States)

    2017-01-20

    Producing uranium-10wt% molybdenum (DU-10Mo) foils to clad with Al first requires initial bonding of the DU-10Mo foil to zirconium (Zr) by hot rolling, followed by cold rolling to final thickness. Rolling often produces wavy (DU-10Mo)-Zr foils that should be flattened before further processing, as any distortions could affect the final alignment and bonding of the Al cladding to the Zr co-rolled surface layer; this bonding is achieved by a hot isostatic pressing (HIP) process. Distortions in the (DU-10Mo)-Zr foil may cause the fuel foil to press against the Al cladding and thus create thinner or thicker areas in the Al cladding layer during the HIP cycle. Post machining is difficult and risky at this stage in the process since there is a chance of hitting the DU-10Mo. Therefore, it is very important to establish a process to flatten and remove any waviness. This study was conducted to determine if a simple annealing treatment could flatten wavy foils. Using the same starting material (i.e. DU-10Mo coupons of the same thickness), five different levels of hot rolling and cold rolling, combined with five different annealing treatments, were performed to determine the effect of these processing variables on flatness, bonding of layers, annealing response, microstructure, and hardness. The same final thickness was reached in all cases. Micrographs, textures, and hardness measurements were obtained for the various processing combinations. Based on these results, it was concluded that annealing at 650°C or higher is an effective treatment to appreciably reduce foil waviness.

  11. Plutonium working group report on environmental, safety and health vulnerabilities associated with the department's plutonium storage. Volume II, part 6: Lawrence Livermore National Laboratory working group assessment team report

    International Nuclear Information System (INIS)

    1994-09-01

    President Clinton directed an Interagency Working Group to initiate a comprehensive review of long-term options for the disposition of surplus plutonium. As part of this initiative, Secretary of Energy Hazel O'Leary directed the Department of Energy to develop options and plans for the interim safe storage of these materials. One step in this direction is a plutonium vulnerability assessment of DOE facilities by a open-quotes Plutonium Vulnerability Working Group.close quotes In this effort, the working group developed a Project Plan and an Assessment Plan which basically laid out the approach and methodology for the assessments. The plans were issued on April 25, 1994. The Project Plan specifies a WGAT for each site with significant holdings of plutonium. Also, the plan requires that each site form a Site Assessment Team (SAT) to provide the self assessment for the project. Additionally, the working group was tasked with managing the assessments at each site, and providing the results in a final report for the Secretary by September 30, 1994

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

    International Nuclear Information System (INIS)

    Krauth, A.; Mueller, N.

    1977-01-01

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

  13. Monitoring the risks of plutonium

    International Nuclear Information System (INIS)

    Holliday, B.

    1978-01-01

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

  14. Progress on plutonium stabilization

    Energy Technology Data Exchange (ETDEWEB)

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

    1996-05-01

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

  15. Progress on plutonium stabilization

    International Nuclear Information System (INIS)

    Hurt, D.

    1996-01-01

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

  16. Adjustment of a direct method for the determination of man body burden in Pu-239 on by X-ray detection of U-235; Mise au point d'une methode directe de determination de la charge corporelle en plutonium 239 chez l'homme par detection X de l'uranium 235

    Energy Technology Data Exchange (ETDEWEB)

    Boulay, P [Commissariat a l' Energie Atomique, Bruyeres-le-Chatel (France). Centre d' Etudes

    1968-04-01

    The use of Pu-239 on a larger scale sets a problem about the contamination measurement by aerosol at lung level. A method of direct measurement of Pu-239 lung burden is possible, thanks to the use of a large area window proportional counter. A counter of such pattern, has been especially carried out for this purpose. The adjustment of the apparatus allows an adequate sensibility to detect a contamination at the maximum permissible body burden level. Besides, a method for individual 'internal calibration', with a plutonium mock: the protactinium-233, is reported. (author) [French] L'utilisation a une echelle de plus en plus large du plutonium-239 pose un probleme de la mesure de la contamination par aerosol au niveau du poumon. Une methode de mesure directe de la charge pulmonaire en plutonium-239 est possible grace a l'utilisation d'un compteur proportionnel a fenetre de grande surface. Un compteur de ce type a specialement ete realise dans ce but. La mise au point de l'appareillage permet une sensibilite suffisante pour deceler une contamination au niveau de la Q.M.A (quantite maximale admissible). D'autre part, une methode 'd'etalonnage interne' de l'individu a l'aide d'un simulateur de plutonium, le protactinium-233, est decrite. (auteur)

  17. Excess Weapons Plutonium Immobilization in Russia

    International Nuclear Information System (INIS)

    Jardine, L.; Borisov, G.B.

    2000-01-01

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

  18. Plutonium recovery from carbonate wash solutions

    International Nuclear Information System (INIS)

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

    1991-01-01

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

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

    International Nuclear Information System (INIS)

    Barth, J.

    1975-01-01

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

  20. Plutonium metal burning facility

    International Nuclear Information System (INIS)

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

    1977-01-01

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

  1. 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

  2. Non-fertile fuels for burning weapons plutonium in thermal fission reactors

    International Nuclear Information System (INIS)

    Lombardi, C.; Mazzola, A.; Vettraino, F.

    1996-01-01

    Waste (HLW) suitable for final disposal in the deep geological formations without requiring any further reprocessing treatment (once-through solution). The fuel pellets, similar to those currently employed in the commercial LWR's will come from the ceramic mixed powders technology or from Gel Supported Precipitation (GSP) microsphere process. The neutronic calculations show that commercial PWRs partially fed with Pu-inert matrix fuel and operated in a once-through cycle, have good plutonium elimination capabilities. The plutonium still remaining in the spent fuel is quality-poor, difficult to be recovered and then highly proliferation resistant. Radiotoxicity levels versus time in inert matrix spent fuel, do not show any increase with respect to standard unreprocessed spent fuel. A most relevant open issue is, however, the technological development and qualification of this new fuel. (author)

  3. Plutonium isotopic measurements by gamma-ray spectroscopy

    International Nuclear Information System (INIS)

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

    1976-01-01

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

  4. A perspective on safeguarding and monitoring of excess military plutonium

    International Nuclear Information System (INIS)

    Sutcliffe, W.G.

    1994-01-01

    The purpose of this paper is to provide a perspective and framework for the development of safeguarding and monitoring procedures for the various stages of disposition of excess military plutonium. The paper briefly outlines and comments on some of the issues involved in safeguarding and monitoring excess military plutonium as it progresses from weapons through dismantlement, to fabrication as reactor fuel, to use in a reactor, and finally to storage and disposal as spent fuel. open-quotes Militaryclose quotes refers to ownership, and includes both reactor-grade and weapon-grade plutonium. open-quotes Excessclose quotes refers to plutonium (in any form) that a government decides is no longer needed for military use and can be irrevocably removed from military stockpiles. Many of the issues and proposals presented in this paper are based on, or are similar to, those mentioned in the National Academy of Sciences (NAS) report on excess military plutonium. Safeguards for plutonium disposition are discussed elsewhere in terms of requirements established by the U.S. Department of Energy (DOE), the U.S. Nuclear Regulatory Commission (NRC), and the International Atomic Energy Agency (IAEA). Here, the discussion is less specific. The term open-quotes safeguardingclose quotes is used broadly to refer to materials control and accountancy (MC ampersand A), containment and surveillance (C ampersand S), and physical protection of nuclear materials by the state that possesses those materials. This is also referred to as material protection, control, and accountancy (MPCA). The term open-quotes safeguardingclose quotes was chosen for brevity and to distinguish MPCA considered in this paper from international or IAEA safeguards. open-quotes Monitoringclose quotes is used to refer to activities designed to assure another party (state or international organization) that the nuclear materials of the host state (the United States or Russia) are secure and not subject to unauthorized

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1958-07-01

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

  6. Plutonium speciation affected by environmental bacteria

    International Nuclear Information System (INIS)

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

    2005-01-01

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

  7. Plutonium vulnerability issues at Hanford's Plutonium Finishing Plant

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  8. Physics of Plutonium Recycling in Thermal Reactors

    International Nuclear Information System (INIS)

    Kinchin, G.H.

    1967-01-01

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

  9. Physics of Plutonium Recycling in Thermal Reactors

    Energy Technology Data Exchange (ETDEWEB)

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

    1967-09-15

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

  10. Cigarette smoke and plutonium

    International Nuclear Information System (INIS)

    Filipy, R.E.

    1982-01-01

    The major objective of this project is to obtain experimental data that are directly applicable to resolving the question of whether cigarette smokers are at greater risk than nonsmokers to potential health effects of inhaled plutonium. Progress was made on two fronts during the past year. The autoradiographic technique developed from detection of plutonium on the interior surface of pulmonary airways (Annual Report, 1978) has been adapted to routine use in examining tracheas and bronchi of rats. Also, dogs exposed to cigarette smoke for over a year after inhalation of plutonium were killed and necropsied

  11. Plutonium inventories for stabilization and stabilized materials

    Energy Technology Data Exchange (ETDEWEB)

    Williams, A.K.

    1996-05-01

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

  12. Combined evaluation. Plutonium transports in France. Problems of safety and reliability of transport container FS47; Evaluation Conjointe. Transports de plutonium en France. Problemes de surete et de securite du container de transport FS47

    Energy Technology Data Exchange (ETDEWEB)

    Marignac, Y.; Coeytaux, X. [Wise-Paris, 75 (France); Large, J.H. [Nuclear Engineer, Large and Associates, Londres (United Kingdom)

    2004-09-15

    This report concerns the safety and the protection of plutonium dioxide transported from Cogema La Hague to the mixed oxide fuel plant of Marcoule and Cadarache. The French approach of the transport safety is based on the combining of two essential principles: the first one affirms that the performances of the FS47 container in regard of containment (norms TS-R-1 from IAEA for the accidental conditions) is conceived to resist in any situation even terrorism or sabotage. In fact, the IAEA norm follows a probabilistic study without a voluntary attack such a terrorist one. The second principle rests on the ability to prevent the treat of terrorism acts, because of a secrecy policy on the plutonium transport. It appeared that the Green peace association has succeeded several times to know exactly the hours, the trips of the plutonium transport and this simple thing raises more questions than it solves. (N.C.)

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

    International Nuclear Information System (INIS)

    Pendharkar, K.A.; Krishnamony, S.

    1983-01-01

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

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

    International Nuclear Information System (INIS)

    Sanders, S.M. Jr.

    1976-11-01

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

  15. Plutonium use - present status and perspectives

    International Nuclear Information System (INIS)

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

    1977-01-01

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

  16. Plutonium biokinetics in humans

    International Nuclear Information System (INIS)

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

    1994-01-01

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

  17. Cigarette smoke and plutonium

    International Nuclear Information System (INIS)

    Anon.

    1981-01-01

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

  18. Decontamination and decommissioning criteria for use in design of new plutonium facilities

    International Nuclear Information System (INIS)

    Paschall, R.K.

    1975-01-01

    Decontamination and decommissioning (D and D) criteria were assembled for use in designing new plutonium facilities. These criteria were gathered from literature searches and visits to many plutonium facilities around the country. The recommendations of reports and experienced personnel were used. Since total D and D costs can be millions of dollars, improved designs to facilitate D and D will result in considerable savings in cost and time and will help to leave the site for unrestricted future use after D and D. Finally, better design will reduce hazards and improve safety during the D and D effort

  19. Disposition of plutonium as non-fertile fuel for water reactors

    International Nuclear Information System (INIS)

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

    1998-01-01

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

  20. Economic considerations of plutonium utilization in the nuclear power strategy of Finland

    International Nuclear Information System (INIS)

    Silvennoinen, P.; Tusa, E.; Routti, J.T.

    1977-01-01

    Based on the current and predicted share of nuclear power in the national energy supply strategy, an optimal programme is developed for the exploitation of plutonium in both light-water and fast reactor systems. Assuming cost trends beyond the year 2000 for uranium, plutonium, uranium enrichment, fuel fabrication and assessing the availability of plutonium from domestic power plants and from abroad, the nuclear construction programme is optimized economically in view of the estimated development in the investment costs of various plant types. Given the expected nuclear share of the energy procurement this sector is covered by the alternative production schemes, i.e. light-water reactors with and without plutonium recycle, and fast reactors. Defining the objective function in terms of minimized revenue requirement in plant amortization and operation the generated scenarios are screened off and they finally converge to the optimal policy of nuclear power construction up to the year 2000. The established technology is associated with a larger share of the domestic manufacturing and the introduction of a new fuel or reactor type is taken to correspond to a reduced domestic investment share. In the investment costs the domestic fraction is regarded competitive up to a certain marginal excess. Plutonium recycle is seen to be competitive from 1985 or as soon as the required amount of fuel has been reprocessed. The domestic accumulation of plutonium will be able to support the introduction of the LMFBR in 1997. Owing to the uncertainties prevailing in the forecasts, sensitivity studies are performed as functions of the major economic parameters and their temporal development. (author)

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

    International Nuclear Information System (INIS)

    1994-11-01

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

  2. A World made of Plutonium?

    International Nuclear Information System (INIS)

    Broda, E.

    1976-01-01

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

  3. Using Biomolecules to Separate Plutonium

    Science.gov (United States)

    Gogolski, Jarrod

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

  4. History of the US weapons-usable plutonium disposition program leading to DOE's record of decision

    International Nuclear Information System (INIS)

    Spellman, D.J.; Thomas, J.F.; Bugos, R.G.

    1997-04-01

    This report highlights important events and studies concerning surplus weapons-usable plutonium disposition in the United States. Included are major events that led to the creation of the U.S. Department of Energy (DOE) Office of Fissile Materials Disposition in 1994 and to that DOE office issuing the January 1997 Record of Decision for the Storage and Disposition of Weapons-Useable Fissile Materials Final Programmatic Environmental Impact Statement. Emphasis has been given to reactor-based plutonium disposition alternatives

  5. Study of a spectrophotometric method of plutonium determination in the organic phase

    International Nuclear Information System (INIS)

    Brutus, Andre

    1971-03-01

    The aim of this paper is to study a method of determining plutonium in the 'Purex' process organic phase, the minimum concentrations to be measured being about 10 -5 M. Spectrophotometry, at 665 nm, of the plutonium arsenazo III complex was carried out directly in the organic phase. Several complexes can be formed between arsenazo III and plutonium; the conditions under which a single complex is obtained, and also those for which this latter follows Beer's law, were determined. The nature and stability of the complex formed were studied, after which it was possible to calculate the equilibrium constant and the standard free enthalpy variation. The field application of the method was established from calculation of the regression line, the confidence limits, the detection limit and the sensitivity. Finally the principle of the elimination of certain troublesome cations in the medium involved was considered. (author) [fr

  6. Granulometric study of plutonium oxide particles in suspension in the atmosphere of a furnace enclosure during the preparation of U-Pu alloys; Etude granulometrique des particules d'oxyde de plutonium en suspension dans l'atmosphere d'une enceinte de fonderie pendant la fabrication d'alliages U-PU

    Energy Technology Data Exchange (ETDEWEB)

    Bataller, G; Lenkauer, S [Commissariat a l' Energie Atomique, Cadarache (France). Centre d' Etudes Nucleaires

    1964-07-01

    Since the extent of an internal contamination by respiration depends on the diameter of the radioactive particles in the atmosphere, a particle size study has been made of the particles present in the air of a working enclosure at the Plutonium Fuel Element Production Section during the preparation of Uranium Plutonium alloy bars. The air of this vessel is drawn through a glass fibre filter on which the dust is deposited. On these filters the radioactive particles are localized first of all by the luminous spots which they produce on a photographic plate when a scintillator is interposed (silver-activated zinc sulphide). An autoradiographic method then makes it possible to distinguish between, and to measure the particles of the oxides of uranium 235, uranium 238 and plutonium 239. On carrying out a microscopic scanning of the relevant parts of the filter, particles are seen surrounded by radial marks the length of which indicates the nature of the grains, and the number of which makes it possible to calculate the theoretical diameter of the radioactive grain. This latter can be compared with the diameter observed with the microscope. Thus for each category of particles it is possible to define a mean diameter and therefore to predict the path of the various inhaled particles in the human body. These results are compared with the very few weakly positive biological samples taken from the personnel working in this enclosure. (authors) [French] L'importance d'une contamination interne par inhalation etant fonction du diametre des particules radioactives en suspension dans l'atmosphere, une etude granulometrique a ete effectuee sur les poussieres existant dans l'air d'une enceinte de travail a la Section de Fabrication des Elements Combustibles au Plutonium pendant une fabrication de barreaux d'alliage Uranium Plutonium, L'air de ce caisson est aspire a travers un filtre en fibre de verre sur lequel restent fixees les poussieres. Sur ces filtres, les particules

  7. 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

  8. Technological alternatives for plutonium transport

    International Nuclear Information System (INIS)

    1978-12-01

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

  9. Gamma spectrometric methods for measuring plutonium

    International Nuclear Information System (INIS)

    Gunnink, R.

    1978-01-01

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

  10. Final generic environmental statement on the use of recycle plutonium in mixed oxide fuel in light water cooled reactors. Volume 2

    International Nuclear Information System (INIS)

    1976-08-01

    This environmental statement assesses the impacts of the implementation of plutonium recycle in the LWR industry. It is based on assumptions that are intended to reflect conservatively an acceptable level of the application of current technology. It is not intended to be a representation of the ''as low as reasonably achievable'' (ALARA) philosophy. This generic environmental statement discusses the anticipated effects of recycling plutonium in light water nuclear power reactors. It is based on about 30 years of experience with the element in the context of a projected light water nuclear power industry that is already substantial. A background perspective on plutonium, its safety, and its recycling as a reactor fuel is presented

  11. Plutonium

    Energy Technology Data Exchange (ETDEWEB)

    Miner, William N

    1964-01-01

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

  12. Plutonium Vulnerability Management Plan

    International Nuclear Information System (INIS)

    1995-03-01

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

  13. The manufacture of plutonium fuels for light water reactors

    International Nuclear Information System (INIS)

    Lebastard, G.

    1985-01-01

    This paper describes the agreement concluded between COGEMA and BELGONUCLEAIRE, reflected in the creation of the COMMOX group which has been made reponsible for promoting and marketing plutonium fuel rods for light water reactors. One then analyses the main aspects of manufacturing this type of fuel and the resources deployed. Finally one indicates the sales prospects scheduled to meet requirements (MELOX plant) [fr

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1959-07-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1959-07-01

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

  16. 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)

  17. Radiological safety aspects of handling plutonium

    International Nuclear Information System (INIS)

    Sundararajan, A.R.

    2016-01-01

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

  18. Plutonium-induced lymphadenitis in beagles

    International Nuclear Information System (INIS)

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

    1976-01-01

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

  19. Guidelines for international plutonium management: Overview and implications

    International Nuclear Information System (INIS)

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

    1998-01-01

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

  20. Six-kilogram-scale electrorefining of plutonium metal

    International Nuclear Information System (INIS)

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

    1982-09-01

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

  1. Erosional losses of fallout plutonium

    International Nuclear Information System (INIS)

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

    1987-01-01

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

  2. Plutonium story

    International Nuclear Information System (INIS)

    Seaborg, G.T.

    1981-09-01

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

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

    International Nuclear Information System (INIS)

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

    1998-01-01

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

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

    International Nuclear Information System (INIS)

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

    1987-01-01

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

  5. An Improved Plutonium Trifluoride Precipitation Flowsheet

    Energy Technology Data Exchange (ETDEWEB)

    Harmon, H.D.

    2001-06-26

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

  6. An Improved Plutonium Trifluoride Precipitation Flowsheet

    International Nuclear Information System (INIS)

    Harmon, H.D.

    2001-01-01

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

  7. Un nouvel habitat du Bronze final IIIb dans le Val d’Orléans et ses traces de métallurgie du fer : Bonnée, Les Terres à l’Est du Bourg (Centre, Loiret A new settlement from late Bronze IIIb in the val d’Orléans: Bonnée, Les Terres à l’Est du Bourg (lands to the east of the town (Centre, Loiret

    Directory of Open Access Journals (Sweden)

    Stéphane Joly

    2011-12-01

    Full Text Available La multiplication récente des diagnostics archéologiques autour du petit bourg actuel de Bonnée a permis la détection d’une occupation du Bronze final IIIb (circa 900-750 av. n.-e. sur environ un hectare aux Terres à l’Est du Bourg. Les limites inhérentes à ce type d’intervention réduisent l’interprétation des structures et toute approche spatiale de ce probable habitat repéré. L’étude conjointe des différents mobiliers en particulier céramique et métallurgique, mais aussi le torchis et la faune, atteste de sa culture matérielle et de son intérêt. Ces scories pourraient être parmi les plus anciennes traces en région Centre d’activité métallurgique du fer. Des activités de post-réduction sont avérées et certaines opérations de forgeage sont supposées.La découverte de cet habitat dans ce secteur du lit majeur de la Loire, apporte de nouvelles données concernant l’occupation du sol et ses problématiques évolutives dans le Val d’Orléans sur ces périodes de transition avec le Hallstatt ancien.The recent increase in the archaeological evaluations around the village of Bonnée has enabled the discovery of a final Bronze Age IIIb settlement (circa 900-750 BP on about a hectare of the Terres à l’Est du Bourg. The limits inherent in this type of work restrict the interpretation of structures and all spatial approaches to this likely dwelling. The joint study of the different furnishings, in particular ceramics and metal, but also the cob and fauna, attests to its material culture and its interest. The slag could be amongst the oldest iron metallurgy remains from the Centre region. Some activities of post-forging are proven and certain operations are guessed at. The discovery of this settlement in this sector of the major bed of the Loire, has produced new data concerning the occupation of the land and its evolutionary problems in the valley of Orleans over these periods of transition in the early

  8. Plutonium valence state distributions

    International Nuclear Information System (INIS)

    Silver, G.L.

    1974-01-01

    A calculational method for ascertaining equilibrium valence state distributions of plutonium in acid solutions as a function of the plutonium oxidation number and the solution acidity is illustrated with an example. The method may be more practical for manual use than methods based upon polynomial equations. (T.G.)

  9. PRISM reactor. An option for plutonium disposition?

    Energy Technology Data Exchange (ETDEWEB)

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

    2015-07-01

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

  10. Plutonium working group report on environmental, safety and health vulnerabilities associated with the department's plutonium storage. Volume II, part 12: Working group assessment team report

    International Nuclear Information System (INIS)

    1994-09-01

    The Secretary of Energy's memorandum of March 15, 1994, established an initiative for a Department-wide assessment of the ES ampersand H vulnerabilities of the inventory of plutonium (Pu) in storage. Pu in intact nuclear weapons, spent fuel and transuranic (TRU) waste not colocated with other Pu was excluded from this assessment. The DOE Plutonium Vulnerability Working Group, which was formed for this purpose and produced the Project and Assessment Plans, will also manage the overall DOE complex assessments and produce a final report for the Secretary of Energy by September 30, 1994. The Project Plan and Assessment Plan for this assessment, and which established responsibilities for personnel essential to the study, were issued on April 25, 1994. This report contains the assessment of the Pantex Plant

  11. The first milligrams of plutonium

    International Nuclear Information System (INIS)

    Goldschmidt, B.

    1996-01-01

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

  12. 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

  13. A host phase for the disposal of weapons plutonium

    International Nuclear Information System (INIS)

    Lutze, Werner; Helean, K.B.; Gong, W.L.; Ewing, Rodney C.

    1999-01-01

    Research was conducted into the possible use of zircon (ZrSiO 4 ) as a host phase for storage or disposal of excess weapons plutonium. Zircon is one of the most chemically durable minerals. Its structure can accommodate a variety of elements, including plutonium and uranium. Natural zircon contains uranium and thorium together in different quantities, usually in the range of less than one weight percent up to several weight percent. Zircon occurs in nature as a crystalline or a partially to fully metamict mineral, depending on age and actinide element concentration, i.e., on radiation damage. These zircon samples have been studied extensively and the results are documented in the literature in terms of radiation damage to the crystal structure and related property changes, e.g., density, hardness, loss of uranium and lead, etc. Thus, a unique suite of natural analogues are available to describe the effect of decay of 239 Pu on zircon's structure and how zircon's physical and chemical properties will be affected over very long periods of time. Actually, the oldest zircon samples known are over 3 billion years old. This period covers the time for decay of 239 Pu (half-life 24,300 yr.) and most of its daughter 235 U (half-life 700 million yr.). Because of its chemical durability, even under extreme geological conditions, zircon is the most widely used mineral for geochronological dating (7,000 publications). It is the oldest dated mineral on earth and in the universe. Zircon has already been doped with about 10 weight percent of plutonium. Pure PuSiO 4 has also been synthesized and has the same crystal structure as zircon. However, use of zircon as a storage medium or waste form for plutonium requires further materials characterization. Experiments can either be conducted in laboratories where plutonium can be handled or plutonium can be simulated by other elements, and experiments can be done under less restricted conditions. The authors conducted work with zircon

  14. Plutonium production and utilization forecasts in Europe

    International Nuclear Information System (INIS)

    Haijtink, B.

    1976-01-01

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

  15. Interim Storage of Plutonium in Existing Facilities

    International Nuclear Information System (INIS)

    Woodsmall, T.D.

    1999-01-01

    'In this era of nuclear weapons disarmament and nonproliferation treaties, among many problems being faced by the Department of Energy is the safe disposal of plutonium. There is a large stockpile of plutonium at the Rocky Flats Environmental Technology Center and it remains politically and environmentally strategic to relocate the inventory closer to a processing facility. Savannah River Site has been chosen as the final storage location, and the Actinide Packaging and Storage Facility (APSF) is currently under construction for this purpose. With the ability of APSF to receive Rocky Flats material an estimated ten years away, DOE has decided to use the existing reactor building in K-Area of SRS as temporary storage to accelerate the removal of plutonium from Rocky Flats. There are enormous cost savings to the government that serve as incentive to start this removal as soon as possible, and the KAMS project is scheduled to receive the first shipment of plutonium in January 2000. The reactor building in K-Area was chosen for its hardened structure and upgraded seismic qualification, both resulting from an effort to restart the reactor in 1991. The KAMS project has faced unique challenges from Authorization Basis and Safety Analysis perspectives. Although modifying a reactor building from a production facility to a storage shelter is not technically difficult, the nature of plutonium has caused design and safety analysis engineers to make certain that the design of systems, structures and components included will protect the public, SRS workers, and the environment. A basic overview of the KAMS project follows. Plutonium will be measured and loaded into DOT Type-B shipping packages at Rocky Flats. The packages are 35-gallon stainless steel drums with multiple internal containment boundaries. DOE transportation vehicles will be used to ship the drums to the KAMS facility at SRS. They will then be unloaded, stacked and stored in specific locations throughout the

  16. Strategies for the plutonium utilization

    International Nuclear Information System (INIS)

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

    1981-11-01

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

  17. Automation of plutonium spectrophotometry

    International Nuclear Information System (INIS)

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

    1980-01-01

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

  18. Civil plutonium amounts in the world

    International Nuclear Information System (INIS)

    Naudet, G.

    1994-01-01

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

  19. Geomorphology of plutonium in the Northern Rio Grande

    Energy Technology Data Exchange (ETDEWEB)

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

    1993-03-01

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

  20. Geomorphology of plutonium in the Northern Rio Grande

    International Nuclear Information System (INIS)

    Graf, W.L.

    1993-03-01

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

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

    International Nuclear Information System (INIS)

    Ochsenfeld, W.; Schmieder, H.

    1976-01-01

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

  2. Experimental Studies on Plutonium Kinetics in Marine Biota

    International Nuclear Information System (INIS)

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

    1976-01-01

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

  3. Experimental studies on plutonium kinetics in marine biota

    International Nuclear Information System (INIS)

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

    1975-01-01

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

  4. 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.)

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

    International Nuclear Information System (INIS)

    Vaidyanathan, S.; Natarajan, P.R.

    1977-01-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1987-09-01

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

  7. Final generic environmental statement on the use of recycle plutonium in mixed oxide fuel in light water cooled reactors. Volume 4

    International Nuclear Information System (INIS)

    1976-08-01

    Information concerning the use of plutonium recycle in water cooled reactors is presented under the following chapter headings: probable adverse environmental effects that cannot be avoided; means for mitigating adverse environmental effects; alternative dispositions of plutonium; relationship between local short term uses of man's environment and the maintenance and enhancement of long term productivity; irreversible and irretrievable commitments of resources; and economic analysis and cost-benefit balancing

  8. Electrochemistry of plutonium in molten halides

    International Nuclear Information System (INIS)

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

    1987-01-01

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

  9. The Plutonium Temperature Effect Experimental Program

    Energy Technology Data Exchange (ETDEWEB)

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

    2008-07-01

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

  10. The distribution of plutonium-241 in rodents

    International Nuclear Information System (INIS)

    Priest, N.D.

    1977-01-01

    Plutonium-241 citrate solution at pH 6.5 was injected intravenously or intraperitoneally into hamsters and rats at a dose of 50 MBq kg -1 (1.35 mCi kg -1 ). The animals were killed 1 day or 1 week later, and tissues were removed for autoradiography and radiochemical analysis. Plutonium-241 was distributed in rats in the same way as plutonium-239, and is a suitable isotope for high-resolution tissue-section autoradiography. Plutonium deposits in cells consisted of a nuclear and a cytoplasmic component. In the hamster kidney cells, the amount associated with the nucleus was about 55 per cent of the total cellular plutonium at 24 hours after injection. Six days later, it was only about 30 per cent. Plutonium deposits were also characterized in hepatocytes, in the interstitial cells of the testes, in the cells of ovarian follicles, in chondrocytes and in bone cells, including osteoblasts and osteocytes. In bone there appeared to be both an extracellular and intracellular deposit. No evidence was found of substantial incorporation of plutonium into the mineral phase of bone. (author)

  11. Plutonium Speciation, Solubilization and Migration in Soils

    International Nuclear Information System (INIS)

    Neu, M.; Runde, W.

    1999-01-01

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

  12. Recent trends of plutonium facilities and their control

    Energy Technology Data Exchange (ETDEWEB)

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

    1974-02-01

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

  13. Plutonium Oxide Process Capability Work Plan

    Energy Technology Data Exchange (ETDEWEB)

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

    2014-02-28

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

  14. Weapons-grade plutonium dispositioning. Volume 1: Executive summary

    International Nuclear Information System (INIS)

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

    1993-06-01

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

  15. Long time contamination from plutonium

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  16. Plutonium gastrointestinal absorption by adults baboons

    International Nuclear Information System (INIS)

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

    1991-01-01

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

  17. Screening study for evaluation of the potential for system 80+ to consume excess plutonium - Volume 1. Final report

    Energy Technology Data Exchange (ETDEWEB)

    1994-04-30

    As part of the U.S. effort to evaluate technologies offering solutions for the safe disposal or utilization of surplus nuclear materials, the fiscal year 1993 Energy and Water Appropriations legislation provided the Department of Energy (DOE) the necessary funds to conduct multi-phased studies to determine the technical feasibility of using reactor technologies for the triple mission of burning weapons grade plutonium, producing tritium for the existing smaller weapons stockpile, and generating commercial electricity. DOE limited the studies to five advanced reactor designs. Among the technologies selected is the ABB-Combustion Engineering (ABB-CE) System 80+. The DOE study, currently in Phase ID, is proceeding with a more detailed evaluation of the design`s capability for plutonium disposition.

  18. Screening study for evaluation of the potential for system 80+ to consume excess plutonium - Volume 2. Final report

    Energy Technology Data Exchange (ETDEWEB)

    1994-04-30

    As part of the U.S. effort to evaluate technologies offering solutions for the safe disposal or utilization of surplus nuclear materials, the fiscal year 1993 Energy and Water Appropriations legislation provided the Department of Energy (DOE) the necessary funds to conduct multi-phased studies to determine the technical feasibility of using reactor technologies for the triple mission of burning weapons grade plutonium, producing tritium for the existing smaller weapons stockpile, and generating commercial electricity. DOE limited the studies to five advanced reactor designs. Among the technologies selected is the ABB-Combustion Engineering (ABB-CE) System 80+. The DOE study, currently in Phase ID, is proceeding with a more detailed evaluation of the design`s capability for plutonium disposition.

  19. Disposing of the world's excess plutonium

    International Nuclear Information System (INIS)

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

    1998-01-01

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

  20. Selecting a plutonium vitrification process

    Energy Technology Data Exchange (ETDEWEB)

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

    1996-05-01

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

  1. Plutonium Disposition Now exclamation point

    International Nuclear Information System (INIS)

    Buckner, M.R.

    1995-01-01

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

  2. Decontaminaion of metals containing plutonium and americium

    International Nuclear Information System (INIS)

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

    1979-06-01

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

  3. Nature`s uncommon elements: Plutonium and technetium

    Energy Technology Data Exchange (ETDEWEB)

    Curtis, D.; Fabryka-Martin, J.; Dixon, P. [Los Alamos National Lab., NM (United States). Chemical Science and Technology Div.; Cramer, J. [Atomic Energy of Canada Ltd., Pinawa, Manitoba (Canada). Whiteshell Lab.

    1998-01-06

    The authors have taken advantage of the extremely sensitive method of thermal ionization mass spectrometry to measure technetium and plutonium concentrations in sample masses that are smaller by as much as three orders of magnitude than those used in the early research efforts. The work reported in this paper extends the understanding of the geochemistry of plutonium and technetium by developing detailed descriptions of their associations in well characterized geologic samples, and by using modern neutron-transport modeling tools to better interpret the meaning of the results. Analyses were conducted on samples from three uranium ore deposits selected for their contrasting geochemical environments. The Cigar Lake deposit is an unweathered, unaltered primary ore in a reducing environment which is expected to closely approximate a system that is closed with respect to uranium and its products. The Koongarra deposit is a shallow system, both altered and weathered, subject to active ground water flow. Finally, a sample from the Beaverlodge deposit is included because it is a commercially-available uranium ore standard that allows demonstration of the precision of the analytical results.

  4. Assay of low-level plutonium effluents

    International Nuclear Information System (INIS)

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

    1981-01-01

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

  5. Light water breeder reactor using a uranium-plutonium cycle

    International Nuclear Information System (INIS)

    Radkowsky, A.; Chen, R.

    1990-01-01

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

  6. The determination of plutonium isotopes in environmental samples

    International Nuclear Information System (INIS)

    Siripirom, Lopchai.

    1983-01-01

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

  7. 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)

  8. Nuclear legacy. Democracy in a plutonium economy

    International Nuclear Information System (INIS)

    Barnaby, F.

    1997-01-01

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

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

    International Nuclear Information System (INIS)

    Dupuy, M.

    1967-07-01

    A survey of uranium-plutonium phase diagram leads to confirm anglo-saxon results about the plutonium solubility in α uranium (15 per cent at 565 C) and the uranium one in ζ phase (74 per cent at 565 C). Interdiffusion coefficients, for concentration lower than 15 per cent had been determined in a temperature range from 410 C to 640 C. They vary between 0.2 and 6 10 12 cm 2 s -1 , and the activation energy between 13 and 20 kcal/mole. Grain boundary, diffusion of plutonium in a uranium had been pointed out by micrography, X-ray microanalysis and α autoradiography. Self-diffusion of plutonium in ε phase (bcc) obeys Arrhenius law: D = 2. 10 -2 exp -(18500)/RT. But this activation energy does not follow empirical laws generally accepted for other metals. It has analogies with 'anomalous' bcc metals (βZr, βTi, βHf, U γ ). (author) [fr

  10. Alecto 1 - criticality experiment on a solution of plutonium and of uranium 235. Experimental results and calculations on tank number 2 ({phi} 300 mm); Alecto 1 - experience de criticite sur une solution de plutonium et d'uranium enrichi a 90 pour cent. Resultats experimentaux et calculs concernant la cuve no. 2 ({phi} = 300 mm)

    Energy Technology Data Exchange (ETDEWEB)

    Bruna, J G; Brunet, J P; Clouet D' Orval, Ch; Kremser, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1964-07-01

    Experiments on plutonium and 90 pour cent enriched uranium solutions have been made in the Alecto reactor with a tank of external diameter 300 mm. Various geometries Lave been tested, for variable concentrations of fissionable salts. The critical mass was studied as a function of the concentration in various reflector conditions (water, concrete, wood) and the experimental values were compared with calculated values. The effects of cadmium as a reflector and of the stainless steel tank were also studied. Lastly were carried out measurements of {beta}/{tau}, ratio of the effective fraction of delayed neutrons to the average lifetime of the neutrons in the reactor. (authors) [French] Des experiences sur des solutions de plutonium et d'uranium enrichi a 90 pour cent ont ete effectuees dans le reacteur Alecto, avec une cuve de diametre exterieur 300 mm. Diverses configurations geometriques ont ete realisees, pour des concentrations variables du sel fissile. On a etudie la masse critique en fonction de la concentration, dans plusieurs conditions de reflexion (eau, beton, bois), et on a compare les resultats experimentaux aux valeurs donnees par le calcul. On a egalement etudie l'influence du cadmium comme reflecteur et celle de la cuve d'acier inoxydable. Enfin on a effectue des mesures de {beta}/{tau}, rapport de la proportion effective des neutrons retardes au temps de vie moyen des neutrons dans la pile. (auteurs)

  11. Atomic energy policy of Japan, especially plutonium utilization policy

    International Nuclear Information System (INIS)

    Moriguchi, Y.

    1993-01-01

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

  12. Solubility of plutonium dioxide aerosols, in vitro

    International Nuclear Information System (INIS)

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

    1976-01-01

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

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

    Science.gov (United States)

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

    2014-08-11

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

  14. 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)

  15. An ab initio study of plutonium oxides surfaces

    International Nuclear Information System (INIS)

    Jomard, G.; Bottin, F.; Amadon, B.

    2007-01-01

    By means of first-principles calculations, we have studied the atomic structure as well as the thermodynamic stability of various plutonium dioxide surfaces in function of their environment (in terms of oxygen partial pressure and temperature). All these simulations have been performed with the ABINIT code. It is well known that DFT fails to describe correctly plutonium-based materials since 5f electrons in such systems are strongly correlated. In order to go beyond DFT, we have treated PuO 2 and β-Pu 2 O 3 in a DFT+U framework. We show that the couple of parameters (U,J) that works well for pure Pu is also well designed for describing ground state (GS) properties of these two oxides. The major improvement with respect with DFT is that we are able to predict an insulating GS in agreement with experiments. The presence of a gap in the DOS (Density of States) of plutonium oxides should play a significant role in the predicted surface reactivity. However, performing DFT+U calculations on surfaces of plutonium oxide from scratch was too ambitious. That is why we decided, as a first step, to study the stability of the (100), (110) and (111) surfaces of PuO 2 in a DFT-GGA framework. For each of these orientations, we considered various terminations. These ab initio results have been introduced in a thermodynamic model which allows us to predict the relative stability of the different terminations as a function of temperature and oxygen partial pressure (p O 2 ). We conclude that at room temperature and for p O 2 ∼10 atm., the polar O 2 -(100) termination is favoured. The stabilization of such a polar stoichiometric surface is surprising and should be confirmed by DFT+U calculations before any final conclusion. (authors)

  16. Current status of the plutonium hot particle problem

    International Nuclear Information System (INIS)

    Richmond, C.R.

    1975-01-01

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

  17. 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

  18. 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

  19. Tabulated Neutron Emission Rates for Plutonium Oxide

    Energy Technology Data Exchange (ETDEWEB)

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

    2017-07-24

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

  20. Model of plutonium dynamics in a deciduous forest ecosystem

    International Nuclear Information System (INIS)

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

    1980-01-01

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

  1. Measurements of plutonium in environmental samples

    International Nuclear Information System (INIS)

    D'Alberti, F.; Risposi, L.

    1996-01-01

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

  2. Measurements of plutonium in environmental samples

    Energy Technology Data Exchange (ETDEWEB)

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

    1996-01-01

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

  3. Long time contamination from plutonium

    Energy Technology Data Exchange (ETDEWEB)

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

    1996-12-31

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

  4. Plutonium recycle. In-core fuel management

    International Nuclear Information System (INIS)

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

    1985-01-01

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

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

    International Nuclear Information System (INIS)

    1967-01-01

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

  6. Qualitative chemical analysis of plutonium by Alpha spectroscopy

    International Nuclear Information System (INIS)

    Ramirez G, J Qumica.J.

    1994-01-01

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

  7. 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.

  8. International shipment of plutonium by air

    International Nuclear Information System (INIS)

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

    1995-05-01

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

  9. Soil surface stabilization using an in situ plutonium coating techniuqe at the Nevada Test Site

    International Nuclear Information System (INIS)

    Lew, J.; Snipes, R.; Tamura, T.

    1996-01-01

    The Hazardous Waste Remedial Actions Program (HAZWRAP), in collaboration with the University of Nevada at Reno (UNR), has developed and is investigating an in situ plutonium treatment for soils at the Nevada Test Site (NTS). The concept, conceived by Dr. T. Tamura and refined at HAZWRAP, was developed during the Nevada Applied Ecology Program investigation. In analyzing for plutonium in soils, it was noted that the alpha emanation of plutonium was greatly attenuated if traces of iron or manganese oxides were present in the final electroplating stage. The technique would reduce resuspension of alpha particles into the air by coating the contaminants in soils in situ with an environmentally compatible, durable, and nontoxic material. The coating materials (calcium hydroxide, ferrous sulfate) reduce resuspension by providing a cementitious barrier against radiation penetration while retaining soil porosity. This technique not only stabilizes plutonium-contaminated soils, but also provides an additional protection from worker exposure to radiation during remediation activities. Additionally, the coating would decrease the water solubility of the contaminant and, thus, reduce its migration through soil and uptake by plants

  10. 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

  11. Pulmonary carcinogenesis from plutonium-containing particles

    International Nuclear Information System (INIS)

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

    1980-01-01

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

  12. Verification station for Sandia/Rockwell Plutonium Protection system

    International Nuclear Information System (INIS)

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

    1979-04-01

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

  13. Modified titrimetric determination of plutonium using photometric end-point detection

    International Nuclear Information System (INIS)

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

    1980-04-01

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

  14. The economics of plutonium recycle

    International Nuclear Information System (INIS)

    James, R.A.

    1977-11-01

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

  15. Nondestructive assay of plutonium residue in horizontal storage tanks

    International Nuclear Information System (INIS)

    Marsh, S.F.

    1985-01-01

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

  16. Plutonium uniqueness

    International Nuclear Information System (INIS)

    Silver, G.L.

    1984-01-01

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

  17. [Present conceptions of the C.E.A. concerning] the development of fast neutron reactors in France; [Les conceptions actuelles du C.E.A. concernant] la filiere des reacteurs a neutrons rapides en France

    Energy Technology Data Exchange (ETDEWEB)

    Vendryes, G; Gaussens, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires; Pasquer, R [Electricite de France (EDF), 75 - Paris (France)

    1964-07-01

    . (authors) [French] 1 - Situation des reacteurs a neutrons rapides dans le programme d'energie nucleaire francais. En developpant un programme base sur l'uranium naturel, la France se trouvera dotee d'un stock important de plutonium riche on isotopes superieurs. L'existence de ce plutonium et de l'uranium appauvri provenant des memes reacteurs a pour consequence logique leur emploi dans des reacteurs a neutrons rapides. Justifiee par cet interet a court terme, la mise au point de reacteurs a neutrons rapides repond par ailleurs a une necessite pour l'avenir. 2 - Enonce des caracteristiques d'une centrale a neutrons rapides de 1000 MW el. Nous indiquons les caracteristiques d'une future centrale a neutrons rapides chargee au plutonium et refroidie au sodium. Si incertaines qu'elles soient, elles constituent un guide necessaire a l'orientation de nos travaux. 3 - Etudes effectuees a ce jour: Nous donnons un apercu des etudes souvent tres preliminaires qui ont permis de retenir les caracteristiques citees plus haut. Les principaux domaines techniques abordes sont les suivants: - Neutronique (masses critiques, taux de regeneration, enrichissements, aplatissement du flux de neutrons, coefficients de reactivite, evolution de la reactivite en fonction de l'irradiation), - Dynamique, controle et surete, - Combustible, - Technologie (conception du bloc-pile, des circuits de sodium, des dispositifs pour la manutention des assemblages). Ces etudes techniques se completent de considerations economiques. Le choix de caracteristiques optimales est lie a l'existence de programmes de production d'electricite et, dans ces programmes, a celle des reacteurs a neutrons thermiques producteurs de plutonium. On montre comment il y a lieu de tenir compte de l'existence du plutonium dans ce contexte, et quels sont les mecanismes qui rattachent l'economie de ce plutonium au choix des parametres essentiels des reacteurs surgenerateurs. 4 - Reacteur prototype: On justifie l'interet d'une etape

  18. Determination of plutonium in soils by mass spectrometry

    International Nuclear Information System (INIS)

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

    1974-01-01

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

  19. 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

  20. Magnetic separation as a plutonium residue enrichment process

    International Nuclear Information System (INIS)

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

    1990-01-01

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

  1. 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

  2. Analysis of plutonium-239 in occupationally exposed personnel

    International Nuclear Information System (INIS)

    Hernandez M, H.

    2017-10-01

    Apart from radiometric techniques, several mass spectrometry (Ms) techniques can be used to evaluate the incorporation of plutonium-239 in occupationally exposed personnel, among which we can consider mass spectrometry with inductively coupled plasma source (Icp-Ms); mass spectrometry with accelerators (AMS); thermal ionization mass spectrometry (TIMS) and secondary ion mass spectrometry (Sims). In this work we evaluated analytical methods to measure isotopes of plutonium-239 in urine samples from occupationally exposed personnel, using alpha spectroscopy (As), magnetic sector mass spectrometry with inductively coupled plasma source (Icp-SFMS) and AMS. The samples were collected during 24 h were acidified with HNO 3 at 5% in v/v. The processes used in the preparation of the samples were: a) co-precipitation, b) acid digestion, c) radiochemical separation and d) electro deposition. The results obtained in terms of minimum detectable activity of plutonium-239 were 0.1 μBq (∼ 0.4 fg per sample), 5.1 μBq (∼ 2 fg per sample), 30.1 μBq (∼ 13 fg per sample) and 0.1 μBq (∼ 51 fg per sample) for AMS, Aridus-Icp-SFMS, Icp, SFMS and As, respectively. On the other hand, samples previously analyzed by As were re-evaluated by Aridus-Icp-SFMS and AMS. The results show that extraction with 60 ml of 5% HNO 3 at 60 degrees Celsius and for 2.5 h is enough to extract 90% of Pu electrodeposited on the planchette. In conclusion, AMS is an ultra-sensitive technique for determining isotope ratios of Pu, especially when is desired to validate a method to measure plutonium-239. Additionally, Icp-SFMS is a rapid analysis technique and can be used as a screening technique in situations of radiological incidents or accidents with Pu in the occupationally exposed personnel. Regarding alpha spectroscopy has been considered as the technique of excellence in the routine analysis to measure plutonium-239 in occupationally exposed personnel, due to the low cost. Finally, Icp-SFMS and AMS

  3. Plutonium in the ocean environment. Its distributions and behavior

    International Nuclear Information System (INIS)

    Hirose, Katsumi

    2009-01-01

    Marine environments have been extensively contaminated by plutonium as a result of global fallout due to atmospheric nuclear-weapons testing. Knowledge of the levels and behavior of plutonium in marine environments is necessary to assess the radiological and ecological effects of plutonium. Such analytical techniques as radiochemical analysis, α-spectrometry, and mass spectrometry have been developed to analyze the plutonium in seawater over the past five decades. Because of complex chemical properties (e.g. high reactivity to particles), plutonium in the ocean exhibits more complicated behavior than other long-lived anthropogenic radionuclides, such as 137 Cs. In the present study. In reviewed the research history of plutonium in the ocean, including spatial and temporal changes of plutonium levels and distributions, and its oceanographic behavior. (author)

  4. Study of a plutonium substitute for the reducing back-extraction in low flow rate contactors; Etude d'un substitut du plutonium pour la desextraction reductrice dans des contacteurs a faible temps de sejour

    Energy Technology Data Exchange (ETDEWEB)

    Morell, M

    1998-12-16

    The aim of this work is to define and carry out a non-radioactive redox chemical system, similar to those of the plutonium, in a reducing back-extraction operation. In the first part, we have replaced our study within the context of the spent fuels. The choice of cerium as a plutonium substitute is justified and the used centrifugal drier described. The current process is presented and the set problem explained. The experimental study concerns essentially the research of reducers of the chosen substitute, the stability of ceric solutions, the measurement of distribution coefficients and the study of redox chemical kinetics. In the last part, are given the used simulation tools (development of a mathematical model in a first step and adaptation of the PAREX code in the second step) and the results of their comparison with the experimental data.

  5. Evaluation of plutonium at Enewetak Atoll

    International Nuclear Information System (INIS)

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

    1975-01-01

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

  6. Long-term plutonium storage: Design concepts

    International Nuclear Information System (INIS)

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

    1994-01-01

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

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

    International Nuclear Information System (INIS)

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

    2000-01-01

    , contained in MOX-fuel, with zirconium alloys and stainless steels is not known. The knowledge of its acceptable content in fuel will permit to choose an optimum variant of plutonium purification from gallium. Therewith, it is possible to guess that the acceptable content of gallium in plutonium dioxide used for fabrication of the fuel for the reactors on fast and thermal neutrons can be different. To furnish the environmental safety of MOX-fuel during its storage, transportation and production, plutonium dioxide must be refined from americium-241, which is being accumulated in weapons-grade plutonium on the account of decaying plutonium-241. At present, in Russia there are several technologies under study, which principally allow to resolve the tasks mentioned above. All technologies have advantages and disadvantages, but none of them can be considered complete since in each one there are fields that are not studied sufficiently, and mainly, in many processes a final result, the quality of plutonium dioxide, is not assessed. Detailed description of some technologies of the conversion is included. These are being studied in scientific centers at MINATOM

  8. 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

  9. Technical considerations and policy requirements for plutonium management

    International Nuclear Information System (INIS)

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

    1995-01-01

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

  10. On-line monitoring of low-level plutonium concentrations

    International Nuclear Information System (INIS)

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

    1979-10-01

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

  11. Technical considerations and policy requirements for plutonium management

    International Nuclear Information System (INIS)

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

    1996-01-01

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

  12. Plutonium again (smuggling and movements)

    International Nuclear Information System (INIS)

    Anon.

    1994-01-01

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

  13. Safe handling of plutonium: a panel report

    Energy Technology Data Exchange (ETDEWEB)

    1974-01-01

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

  14. Plutonium disposition via immobilization in ceramic or glass

    Energy Technology Data Exchange (ETDEWEB)

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

    1997-03-05

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

  15. 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

  16. Plutonium decontamination studies using Reverse Osmosis

    International Nuclear Information System (INIS)

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

    1980-01-01

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

  17. Uranium-plutonium fuel for fast reactors

    International Nuclear Information System (INIS)

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

    1996-01-01

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

  18. 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

  19. The extraction of plutonium with triethylene glycol dichloride

    International Nuclear Information System (INIS)

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

    1951-03-01

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

  20. The extraction of plutonium with triethylene glycol dichloride

    Energy Technology Data Exchange (ETDEWEB)

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

    1951-03-15

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

  1. Study of plutonium multi-recycle in high moderation LWR cores

    International Nuclear Information System (INIS)

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

    2000-01-01

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

  2. Standard practice for preparation and dissolution of plutonium materials for analysis

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    2008-01-01

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

  3. Civil plutonium held in France in December 31, 2000

    International Nuclear Information System (INIS)

    2002-02-01

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

  4. Plutonium determination by isotope dilution

    International Nuclear Information System (INIS)

    Lucas, M.

    1980-01-01

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

  5. Instruments used to measure or check {alpha}, {beta}, {gamma} activity and neutron emission in the course of processing ore or irradiated fuel; Appareils de mesure ou de controle {alpha}, {beta}, {gamma}, n, des circuits des usines de traitement du minerai ou du combustible irradie

    Energy Technology Data Exchange (ETDEWEB)

    Blanc, A; Brunet, M; Kermagoret, M; Labeyrie, J; Roux, G; Vasseur, J; Weil, J [Commissariat a l' Energie Atomique, Saclay (France). Centre d' Etudes Nucleaires

    1959-07-01

    One of the methods checking ores in the course of treatment is the rapid quantitative determination of thorium. This measurement is carried out by means of a scintillation instrument which shows the {beta} and {alpha} coincidences of ThC and ThC'. The treatment of irradiated fuel is accompanied by a large number of radioactive checks relative to the performance of the fixation and elution operations of uranium in the ion exchangers, to the concentration of radioactivity of effluent sent from the plant into watercourses. The operations of fixation and elution of the uranium are checked automatically by an instrument which takes a sample of 5 cm{sup 3} of solution, evaporates it and measures its activity every 10 or 20 minutes. Plutonium concentrations are measured: - in the presence of strong {beta} {gamma} activities, by means of rotating cylinder detectors; - in the presence of weak {beta} {gamma} activities, by means of {alpha} detectors scanning a constant level liquid surface; - by means of fission chambers relatively insensitive to {gamma}. Fission product concentrations are measured by chambers, counters or scintillators, according to the amount of {gamma} activity present. Finally, the activity of effluent to be emptied into watercourses is checked by means of a scintillation instrument, which measures the {alpha} activity on the one hand, and on the other hand the {beta} {gamma} activity of residue from a 100 cm{sup 3} sample taken and evaporated in 20 minutes. (author) [French] Parmi les controles relatifs au minerai en cours de traitement, figure le dosage rapide de thorium. Cette mesure est realisee au moyen d'un appareillage a scintillation qui met en evidence la coincidence des emissions {beta} et {alpha} du ThC et du ThC'. Le traitement des combustibles irradies s'accompagne d'un grand nombre de controles radioactifs portant sur le fonctionnement des operations de fixation et d'elution de l'uranium dans les echangeurs d'ions, sur la concentration du

  6. Plutonium and americium separation from salts

    International Nuclear Information System (INIS)

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

    1976-01-01

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

  7. Work at Aldermaston on plutonium binding with biological systems

    International Nuclear Information System (INIS)

    Popplewell, D.S.

    1976-01-01

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

  8. Distribution coefficient of plutonium between sediment and seawater

    International Nuclear Information System (INIS)

    Duursma, E.K.; Parsi, P.

    1974-01-01

    Using plutonium 237 as a tracer, a series of experiments were conducted to determine the distribution coefficient of plutonium onto sediments both under oxic and anoxic conditions, where the plutonium was added to seawater in three different valence states: III, IV and VI

  9. HENC performance evaluation and plutonium calibration

    International Nuclear Information System (INIS)

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

    1997-10-01

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

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

    Energy Technology Data Exchange (ETDEWEB)

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

    1980-10-01

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

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

    International Nuclear Information System (INIS)

    Grison, J.

    1980-01-01

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

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

    Science.gov (United States)

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

    1997-10-01

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

  13. Plutonium recycle in PWR reactors (Brazilian Nuclear Program)

    International Nuclear Information System (INIS)

    Rubini, L.A.

    1978-02-01

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

  14. Plutonium in a grassland ecosystem

    International Nuclear Information System (INIS)

    Little, C.A.

    1976-01-01

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

  15. Work surface for soluble plutonium

    International Nuclear Information System (INIS)

    Silver, G.L.

    2005-01-01

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

  16. Oxidation-state maxima in plutonium chemistry

    International Nuclear Information System (INIS)

    Silver, G.L.

    2013-01-01

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

  17. Development of an analytical procedure for plutonium in the concentration range of femtogram/gram and its application to environmental samples

    International Nuclear Information System (INIS)

    Schuettelkopf, H.

    1981-09-01

    To study the behaviour of plutonium in the environment and to measure plutonium in the vicinity of nuclear facilities, a quick, sensitive analytical method is required which can be applied to all sample materials found in the environment. For a sediment contaminated with plutonium a boiling out method using first HNO 3 /HF and subsequently HNO 3 /Al(NO 3 ) 3 was found to be successful. The leaching solution was then extracted by TOPO and the plutonium backextracted by ascorbic acid/HCl. Some different purification steps and finally electroplating using ammonium oxalate led to an optimum sample for α- spectroscopic determination of plutonium. An analytical method was worked out for plutonium which can be applied to all materials found in the environment. The sample size is 100 g but it might also be much greater. The average chemical yield is 70 and 80%. The detection limit for soil samples is 0.1 fCi/g and for plant samples 0.5 fCi/g. One technician can perform eight analyses per working day. The analytical procedure was applied to a large number of environmental samples and the results of these analyses are indicated. (orig./RB) [de

  18. Plutonium recycling and the problem of nuclear proliferation

    International Nuclear Information System (INIS)

    Albright, D.; Feiveson, H.S.

    1988-01-01

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

  19. Transport of plutonium in surface and sub-surface waters from the Arctic shelf to the North Pole via the Lomonosov Ridge

    International Nuclear Information System (INIS)

    Leon Vintro, L.; McMahon, C.A.; Mitchell, P.I.; Josefsson, D.; Holm, E.; Roos, P.

    2002-01-01

    New data on the levels and long-range transport of plutonium in the Arctic Ocean, recorded in the course of two expeditions to this zone in 1994 and 1996, are discussed in this paper. Specifically, approximately 100 plutonium measurements in surface and sub-surface water sampled at 58 separate stations throughout the Kara, Laptev and East Siberian Seas, as well as along latitudinal transects across the Lomonosov Ridge, are reported and interpreted in terms of the circulation pathways responsible for the transport of this element from the North Atlantic to the Arctic Shelf and into the Arctic interior. In addition, the behaviour of plutonium in its transit through the vast Arctic shelf seas to open waters under extreme environmental conditions is discussed in terms of the partitioning of plutonium between filtered (<0.45 μm) seawater and suspended particulate, and its association with colloidal matter. Finally, limited evidence of the presence of a colloidal plutonium component in Arctic waters subject to direct riverine input is adduced

  20. 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.

  1. Preparation and application of potassium and sodium titanate for removal of plutonium from basic solution

    International Nuclear Information System (INIS)

    Patil, Prashant; Pathak, Sachin S.; Pius, I.C.; Mukerjee, S.K.

    2014-01-01

    In PUREX process, after extraction and stripping of uranium and plutonium, the extractant, tributyl phosphate is usually washed with sodium carbonate solution before reuse for the removal of radiolytic/hydrolytic degradation products of TBP and small amounts of HNO 3 , uranium and plutonium goes into aqueous phase during carbonate washings. Partial neutralization of carbonate by the acid converts it to bicarbonate. Removal of plutonium from such sodium carbonate/bicarbonate streams facilitates their disposal. In the present work, studies were carried out to prepare inorganic ion-exchangers such as potassium and sodium titanates for their application as ion-exchange material. It is essential to prepare these materials in granular form to obtain good liquid flow property for ion exchange column operations, however, it is also important that the final product is having good surface area and porosity so that they may exhibit good ion exchange capacity

  2. The use of plutonium rapides surregenerateurs aspects techniques et economiques

    International Nuclear Information System (INIS)

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

    1977-01-01

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

  3. Recommendations for plutonium colloid size determination

    International Nuclear Information System (INIS)

    Kosiewicz, S.T.

    1984-02-01

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

  4. Study of a plutonium substitute for the reducing back-extraction in low flow rate contactors; Etude d'un substitut du plutonium pour la desextraction reductrice dans des contacteurs a faible temps de sejour

    Energy Technology Data Exchange (ETDEWEB)

    Morell, M

    1998-12-16

    The aim of this work is to define and carry out a non-radioactive redox chemical system, similar to those of the plutonium, in a reducing back-extraction operation. In the first part, we have replaced our study within the context of the spent fuels. The choice of cerium as a plutonium substitute is justified and the used centrifugal drier described. The current process is presented and the set problem explained. The experimental study concerns essentially the research of reducers of the chosen substitute, the stability of ceric solutions, the measurement of distribution coefficients and the study of redox chemical kinetics. In the last part, are given the used simulation tools (development of a mathematical model in a first step and adaptation of the PAREX code in the second step) and the results of their comparison with the experimental data.

  5. Analytic determination of plutonium in the environment

    International Nuclear Information System (INIS)

    Ballada, J.

    1967-01-01

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

  6. 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.)

  7. Plutonium peroxide precipitation: review and current research

    International Nuclear Information System (INIS)

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

    1980-01-01

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

  8. Fluorescent determination of neptunium in plutonium

    International Nuclear Information System (INIS)

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

    1991-01-01

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

  9. Plutonium Immobilization Can Loading Conceptual Design

    Energy Technology Data Exchange (ETDEWEB)

    Kriikku, E.

    1999-05-13

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

  10. Plutonium Immobilization Can Loading Conceptual Design

    International Nuclear Information System (INIS)

    Kriikku, E.

    1999-01-01

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

  11. Spectrophotometric study of the complexes of cerium and uranides with diethylenetetraaminepentaacetic acid (DTPA); Contribution a l'etude de la complexation du cerium et des uranides par l'acide diethylenetetraminepentaacetique (DTPA)

    Energy Technology Data Exchange (ETDEWEB)

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

    1968-03-01

    A spectrophotometric determination was made of the complexes of cerium and uranides in their different degrees of oxidation with diethylenetriaminepentaacetic acid (DTPA). Two physico-chemical states, the ionic and hydrolysis ones, were considered. In the former case, we studied the influence of the pH on the formation of the complex, and whenever the complexes were stable, we determined the molecular ratio and calculated their stability constants. In the latter case, we studied the conditions of solubilization of the precipitate by formation of complexes soluble in water as a function of pH, age of the precipitate and time of precipitate-chelate contact. (authors) [French] Etude spectrophotometrique de la complexation du cerium et des uranides (uranium, neptunium, plutonium et americium) dans leurs differents etats d'oxydation par l'acide diethylenetriaminepentaacetique (DTPA). Deux etats physicochimiques ont retenu notre attention, l'etat ionique et l'etat precipite d'hydrolyse. Dans le premier cas, nous avons etudie l'influence du pH sur la formation du complexe, et dans tous les cas ou le complexe est stable, nous avons determine le rapport moleculaire (5) [element]/[chelatant] du complexe forme et nous avons calcule leurs constantes de stabilite. Dans le deuxieme cas, l'etat de precipite d'hydrolyse, nous avons etudie les conditions de solubilisation du precipite, par formation du complexe, en fonction du pH, de l'age du precipite et du temps de contact precipite - chelatant. (auteurs)

  12. New developments in the air transport of plutonium

    International Nuclear Information System (INIS)

    Andersen, J.A.

    1978-01-01

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

  13. Trans-Uranium Doping Utilization for Increasing Protected Plutonium Proliferation of Small Long Life Reactor

    Energy Technology Data Exchange (ETDEWEB)

    Permana, Sidik [Research Laboratory for Nuclear Reactors, Tokyo Institute of Technology 2-12-1-N1-17, O-okayama, Meguro-ku, Tokyo 152-8550 (Japan); Nuclear and Biophysics Research Group, Department of Physics, Bandung Institute of Technology, Gedung Fisika, Jl. Ganesha 10, Bandung 40132 (Indonesia); Suud, Zaki [Nuclear and Biophysics Research Group, Department of Physics, Bandung Institute of Technology, Gedung Fisika, Jl. Ganesha 10, Bandung 40132 (Indonesia); Suzuki, Mitsutoshi [Japan Atomic Energy Agency, Nuclear Non-proliferation Science and Technology Center, 2-4 Shirane Shirakata, Tokai-mura, Ibaraki, 319-1195 (Japan)

    2009-06-15

    for different power output and core operation time. The two dimensional core optimization analysis (SRAC-CITATION) has been used with nuclear data library (JENDL-33). Higher plutonium production rate of Pu-238 can be achieved by Neptunium (NP)-237 doping compared with Minor Actinide (MA) doping. However, higher plutonium production rate of Pu-240 can be obtained by MA doping. Pu-238 production decreases and Pu-240 production increases with increasing core operation time for both MA and NP-237 doping materials. In case of different doping rate of MA, it shows Pu-238 and Pu-240 productions are strongly depends on the content of MA doping and different core operation time. Finally, some plutonium characterizations will be shown based on several basic criteria which have been adopted in this study. (authors)

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

    International Nuclear Information System (INIS)

    Priest, N.D.; Hunt, B.W.

    1979-01-01

    Values of the annual limit intake (ALI) for plutonium-239 in man have been calculated using committed dose equivalent limits as recommended by ICRP in Publication 26. The calculations were made using a multicompartment bone model which allows for plutonium burial and recycling in the skeleton. In one skeletal compartment, the growing surfaces of cortical bone, it is assumed that plutonium deposits are retained and are not subject to resorption or recycling. In the trabecular bone compartment plutonium is taken to be resorbed with either subsequent redeposition onto bone surfaces or retention in the bone marrow. ALIs for plutonium-239 have been calculated assuming a range of rates of bone accretion (0 to 32 μm yr -1 ), different amounts of plutonium retained in the marrow (0 to 60%) and a 20%, 45% or 70% deposition of plutonium in the skeleton from the blood. The calculations made using this bone model suggest that 750 Bq (20 nCi) is an appropriate ALI for the inhalation of class W and class Y plutonium compounds and that 830 kBq and 5 MBq (23 μCi and 136 μCi) are the appropriate ALIs for the ingestion of soluble and insoluble forms of plutonium respectively. (author)

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

    Science.gov (United States)

    Priest, N D; Hunt, B W

    1979-05-01

    Values of the annual limit of intake (ALI) for plutonium-239 in man have been calculated using committed dose equivalent limits as recommended by ICRP in Publication 26. The calculations were made using a multicompartment bone model which allows for plutonium burial and recycling in the skeleton. In one skeletal compartment, the growing surfaces of cortical bone, it is assumed that plutonium deposits are retained and are not subject to resorption or recycling. In the trabecular bone compartment plutonium is taken to be resorbed with either subsequent redeposition onto bone surfaces or retention in the bone marrow. ALIs for plutonium-239 have been calculated assuming a range of rates of bone accretion (0-32 micron yr-1), different amounts of plutonium retained in the marrow (0-60%) and a 20%, 45% or 70% deposition of plutonium in the skeleton from the blood. The calculations made using this bone model suggest that 750 Bq (20 nCi) is an appropriate ALI for the inhalation of class W and class Y plutonium compounds and that 830 kBq and 5 MBq (23 muCi and 136 muCi) are the appropriate ALIs for the ingestion of soluble and insoluble forms of plutonium respectively.

  16. Contamination of living environment and human organism with plutonium

    International Nuclear Information System (INIS)

    Benes, J.

    1981-01-01

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

  17. Plutonium Chemistry in the UREX+ Separation Processes

    Energy Technology Data Exchange (ETDEWEB)

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

    2009-10-01

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

  18. Assessment of PWR plutonium burners for nuclear energy centers

    International Nuclear Information System (INIS)

    Frankel, A.J.; Shapiro, N.L.

    1976-06-01

    The purpose of the study was to explore the performance and safety characteristics of PWR plutonium burners, to identify modifications to current PWR designs to enhance plutonium utilization, to study the problems of deploying plutonium burners at Nuclear Energy Centers, and to assess current industrial capability of the design and licensing of such reactors. A plutonium burner is defined to be a reactor which utilizes plutonium as the sole fissile addition to the natural or depleted uranium which comprises the greater part of the fuel mass. The results of the study and the design analyses performed during the development of C-E's System 80 plant indicate that the use of suitably designed plutonium burners at Nuclear Energy Centers is technically feasible

  19. Biological behaviour of plutonium inhaled by baboons as plutonium n-tributylphosphate complex. Comparison with ICRP models

    International Nuclear Information System (INIS)

    Metivier, H.; Duserre, C.; Rateau, G.; Legendre, N.; Masse, R.; Piechowski, J.; Menoux, B.

    1989-01-01

    In order to devise a model capable of calculating committed doses for workers contaminated by inhalation of plutonium tributylphosphate complex during reprocessing, we investigated the biokinetics of plutonium in baboons after inhalation of this chemical form. The animals were killed 0.6, 3, 15, 30, 90 and 365 days post inhalation. Urine and faeces were collected daily. After killing, the main organs were collected for chemical analysis. In order to improve our knowledge of the behaviour of systemic plutonium, three baboons were given an intravenous injection of Pu-TBP and were respectively killed 2, 30 and 365 days post injection. We observed that Pu-TBP could be classified as a W compound, with a half-time for lung clearance of 150 days. Urinary Pu excretion was 3 times higher than was expected from Durbin's model, suggesting that Pu introduced as Pu-TBP, is extremely mobile, and that the complex formed with blood proteins differs from the one formed after inhalation of plutonium nitrate. (author)

  20. Spectrophotometers for plutonium monitoring in HB-line

    Energy Technology Data Exchange (ETDEWEB)

    Lascola, R. J. [Savannah River Site (SRS), Aiken, SC (United States); O' Rourke, P. E. [Savannah River Site (SRS), Aiken, SC (United States); Kyser, E. A. [Savannah River Site (SRS), Aiken, SC (United States); Immel, D. M. [Savannah River Site (SRS), Aiken, SC (United States); Plummer, J. R. [Savannah River Site (SRS), Aiken, SC (United States); Evans, E. V. [Savannah River Site (SRS), Aiken, SC (United States)

    2016-02-12

    This report describes the equipment, control software, calibrations for total plutonium and plutonium oxidation state, and qualification studies for the instrument. It also provides a detailed description of the uncertainty analysis, which includes source terms associated with plutonium calibration standards, instrument drift, and inter-instrument variability. Also included are work instructions for instrument, flow cell, and optical fiber setup, work instructions for routine maintenance, and drawings and schematic diagrams.

  1. Facteurs déterminants de la fragmentation du bloc forêt classée ...

    African Journals Online (AJOL)

    SARAH

    31 mai 2016 ... Original submitted in on 14th March 2016. ... management and reclamation taking into account cultural considerations. .... préféré au coefficient paramétrique de Pearson du fait ...... Version finale du texte publié dans Chrétien.

  2. Plutonium contaminated materials research programme. Progress Report for 1983/84 from the Plutonium Contaminated Materials Working Party

    International Nuclear Information System (INIS)

    Higson, S.G.

    1984-01-01

    Plutonium contaminated material (PCM) is a generic term applied to a wide variety of materials which have become contaminated by plutonium compounds, by virtue of their use inside the primary containment of fuel cycle plants, but which generally have low beta gamma content. The report falls under the headings: introduction; organisation and role of the PCMWP; management practices; 1983/84 progress report (a) reduction of arisings; (b) plutonium measurement; (c) treatment of solid PCM; (d) treatment of alpha bearing liquid wastes; (e) actinide chemistry; (f) engineering objectives. (U.K.)

  3. The radiological hazard of plutonium isotopes and specific plutonium mixtures

    International Nuclear Information System (INIS)

    Heindel, G.; Clow, J.; Inkret, W.; Miller, G.

    1995-11-01

    The US Department of Energy defines the hazard categories of its nuclear facilities based upon the potential for accidents to have significant effects on specific populations and the environment. In this report, the authors consider the time dependence of hazard category 2 (significant on-site effects) for facilities with inventories of plutonium isotopes and specific weapons-grade and heat-source mixtures of plutonium isotopes. The authors also define relative hazard as the reciprocal of the hazard category 2 threshold value and determine its time dependence. The time dependence of both hazard category 2 thresholds and relative hazards are determined and plotted for 10,000 years to provide useful information for planning long-term storage or disposal facilities

  4. 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

  5. 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.

  6. Investigation of plutonium abundance and age analysis

    Energy Technology Data Exchange (ETDEWEB)

    Huailong, Wu; Jian, Gong; Fanhua, Hao [China Academy of Engineering Physics, Mianyang (China). Inst. of Nuclear Physics and Chemistry

    2007-06-15

    Based on spectra analysis software, all of the plutonium material peak counts are analyzed. Relatively efficiency calibration is done by the non-coupling peaks of {sup 239}Pu. By using the known isotopes half life and yield, the coupling peaks counts are allocated by non-coupling peaks, consequently the atom ratios of each isotope are gotten. The formula between atom ratio and abundance or age is deduced by plutonium material isotopes decay characteristic. And so the abundance and age of plutonium material is gotten. After some re- peat measurements for a plutonium equipment are completed, a comparison between our analysis results and PC-FRAM and the owner's reference results are done. (authors)

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

    Science.gov (United States)

    Skipperud, Lindis

    2004-06-18

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

  8. 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

  9. Actes des 5èmes Journées Scientifiques du GDR3544 Sciences du Bois. Journées Annuelles du GDR 3544 Sciences du Bois

    OpenAIRE

    CHAPLAIN, Myriam; CARE, Sabine; GRIL, Joseph

    2016-01-01

    Le Groupement de Recherche en Sciences du bois (GDR3544 Sciences du Bois) a été créé en 2012 par le CNRS et renouvelé en 2016 pour 5 ans. La mission de ce groupement est : (1) de structurer la recherche sur le bois en France pour lui donner une visibilité nationale, (2) de contribuer au développement de la formation en sciences du bois et (3) de servir de relai aux réseaux internationaux de sciences du bois. Les 5èmes journées annuelles du GDR Bois ont été organisées à Bordeaux, au domaine du...

  10. Radiation damage and annealing in plutonium tetrafluoride

    Science.gov (United States)

    McCoy, Kaylyn; Casella, Amanda; Sinkov, Sergey; Sweet, Lucas; McNamara, Bruce; Delegard, Calvin; Jevremovic, Tatjana

    2017-12-01

    A sample of plutonium tetrafluoride that was separated prior to 1966 at the Hanford Site in Washington State was analyzed at the Pacific Northwest National Laboratory (PNNL) in 2015 and 2016. The plutonium tetrafluoride, as received, was an unusual color and considering the age of the plutonium, there were questions about the condition of the material. These questions had to be answered in order to determine the suitability of the material for future use or long-term storage. Therefore, thermogravimetric/differential thermal analysis and X-ray diffraction evaluations were conducted to determine the plutonium's crystal structure, oxide content, and moisture content; these analyses reported that the plutonium was predominately amorphous and tetrafluoride, with an oxide content near ten percent. Freshly fluorinated plutonium tetrafluoride is known to be monoclinic. During the initial thermogravimetric/differential thermal analyses, it was discovered that an exothermic event occurred within the material near 414 °C. X-ray diffraction analyses were conducted on the annealed tetrafluoride. The X-ray diffraction analyses indicated that some degree of recrystallization occurred in conjunction with the 414 °C event. The following commentary describes the series of thermogravimetric/differential thermal and X-ray diffraction analyses that were conducted as part of this investigation at PNNL.

  11. Radiation damage and annealing in plutonium tetrafluoride

    International Nuclear Information System (INIS)

    McCoy, Kaylyn; Casella, Amanda; Sinkov, Sergey

    2017-01-01

    A sample of plutonium tetrafluoride that was separated prior to 1966 at the Hanford Site in Washington State was analyzed at the Pacific Northwest National Laboratory (PNNL) in 2015 and 2016. The plutonium tetrafluoride, as received, was an unusual color and considering the age of the plutonium, there were questions about the condition of the material. These questions had to be answered in order to determine the suitability of the material for future use or long-term storage. Therefore, thermogravimetric/differential thermal analysis and X-ray diffraction evaluations were conducted to determine the plutonium's crystal structure, oxide content, and moisture content; these analyses reported that the plutonium was predominately amorphous and tetrafluoride, with an oxide content near ten percent. Freshly fluorinated plutonium tetrafluoride is known to be monoclinic. And during the initial thermogravimetric/differential thermal analyses, it was discovered that an exothermic event occurred within the material near 414 °C. X-ray diffraction analyses were conducted on the annealed tetrafluoride. The X-ray diffraction analyses indicated that some degree of recrystallization occurred in conjunction with the 414 °C event. This commentary describes the series of thermogravimetric/differential thermal and X-ray diffraction analyses that were conducted as part of this investigation at PNNL.

  12. 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

  13. Plutonium in coniferous forests

    International Nuclear Information System (INIS)

    Rantavaara, A.; Kostiainen, E.

    2002-01-01

    Our aim was to study the uptake of plutonium by trees, undervegetation and some wild foods. The ratio of 238 Pu/ 239,240 Pu in soil samples was determined for comparisons of the fallout origin. In twelve years the Chernobyl derived plutonium has not reached the mineral soil. This refers to a very slow downward migration in podsolic soil. The study confirmed also the low Pu uptake by vegetation and an insignificant contribution to human doses through wild foods. (au)

  14. The first metallurgical tests on plutonium

    International Nuclear Information System (INIS)

    Grison, E.; Abramson, R.; Anselin, F.; Monti, H.

    1958-01-01

    Metallic plutonium was first prepared in France in January 1956, as soon as we had access to quantities of the order of several grams of plutonium, which had been extracted from the rods of the pile EL2 at Saclay. Since up to the present this reactor, of thermal power 2 000 kW, has been our only source of plutonium, we have so far only worked on experimental quantities sufficient for the basic tests but not for tests on a scale of possible applications. It is this work, carried out during this phase of preliminary research, which is described below. With the starting up of the plutonium extraction plant at Marcoule, where the reactor G1 has been operating at power for more than a year, we shall go on next to a another order of magnitude which will allow the manufacture and experimentation of prototype fuel elements. (author) [fr

  15. Plutonium and U-233 mines

    International Nuclear Information System (INIS)

    Milgram, M.S.

    1983-08-01

    A comparison is made among second generation reactor systems fuelled primarily with fissile plutonium and/or U-233 in uranium or thorium. This material is obtained from irradiated fuel from first generation CANDU reactors fuelled by natural or enriched uranium and thorium. Except for plutonium-thorium reactors, second generation reactors demand similar amounts of reprocessing throughput, but the most efficient plutonium burning systems require a large prior allocation of uranium. Second generation reactors fuelled by U-233 make more efficient use of resources and lead to more flexible fuelling strategies, but require development of first generation once-through thorium cycles and early demonstration of the commercial viability of thorium fuel reprocessing. No early implementation of reprocessing technology is required for these cycles

  16. Investigation on the attribute detection of plutonium oxide

    International Nuclear Information System (INIS)

    Liu Suping; Hao Fanhua; Gong Jian; Wu Huailong; Hu Guangchun; Hu Yongbo

    2006-01-01

    A long-term detection of the 871 keV gamma-ray emitted from two PuO 2 samples (100 g recovered powder and 8 g pure powder) has been conduced with a high resolution HPGe spectrometer in a lead-shielded chamber. An on-site detection of the 871 keV gamma-ray emitted from 200 g recovered PuO 2 powder has also been performed. Although the 871 keV peak can be observed in all 3 samples, other characteristic gamma-rays related to the existence of oxygen are not seen. The 871 keV peak is absent in spectra acquired from metal plutonium samples, which can answer whether the plutonium material in a sealed container is metal plutonium or plutonium oxide, i.e. the 871 keV gamma-ray can be an evidence for the absence of metal plutonium. The 871 keV peak is strong in the spectrum of 200 g recovered PuO 2 sample. A software of plutonium abundance and age analysis developed by ourselves can identify the 871 keV peak from a spectrum of 10 min. If the system is appropriately improved, it can be used to detect attribute of plutonium oxide through identifying 871 keV gamma-ray peak. (authors)

  17. Generic environmental statement on the routine use of plutonium-powered cardiac pacemakers

    International Nuclear Information System (INIS)

    Shoup, R.L.; Robinson, T.W.; O'Donnell, F.R.

    1976-01-01

    The purpose of a continuing program at ORNL is to provide technical assistance to the NRC on writing and editing of the final environmental statement on the routine use of nuclear-powered (primarily 238 Pu) cardiac pacemakers. This environmental statement defines the safety and reliability standards that nuclear-powered pacemakers are required to meet. All aspects of the risks to the patients, the public, and the environment are evaluated both for the routine use of plutonium-powered pacemakers and for postulated accidents involving pacemaker patients. Benefits derived from the use of plutonium-powered units are discussed and weighed against the risks in order to determine whether routine use is justified. Available alternative pacemakers with various performance characteristics are compared with respect to costs and to the needs of pacemaker patients

  18. The determination of plutonium alpha activity in urine, faeces and biological materials

    International Nuclear Information System (INIS)

    Bains, M.E.D.

    1963-07-01

    Methods have been developed for the determination of plutonium alpha activity in urine, faeces and biological materials. The chemical stages involved give practically complete separation of all extraneous material from the plutonium, which is electrodeposited on to a 0.5 inch stainless steel disc to produce a thin high resolution source. The limit of detection is 0.025 μμc/sample (sixteen-hour count) when the sources are counted in a small scintillator counter, but is lowest when counted in a counter which counts particles of energy 5.05-5.25 MeV only, and which therefore discriminates against small quantities of α-active materials introduced with the reagents in the final electrodeposition stage of the process. (Any such alpha activity may readily be identified by alpha pulse height analysis). (author)

  19. Physics of plutonium recycling

    International Nuclear Information System (INIS)

    2003-01-01

    The commercial recycling of plutonium as PuO 2 /UO 2 mixed-oxide (MOX) fuel is an established practice in pressurised water reactors (PWRs) in several countries, the main motivation being the consumption of plutonium arising from spent fuel reprocessing. Although the same motivating factors apply in the case of boiling water reactors (BWRs), they have lagged behind PWRs for various reasons, and MOX utilisation in BWRs has been implemented in only a few reactors to date. One of the reasons is that the nuclear design of BWR MOX assemblies (or bundles) is more complex than that of PWR assemblies. Recognizing the need and the timeliness to address this issue at the international level, the OECD/NEA Working Party on the Physics of Plutonium Fuels and Innovative Fuel Cycles (WPPR) conducted a physics code benchmark test for a BWR assembly. This volume reports on the benchmark results and conclusions that can be drawn from it. (authors)

  20. Plutonium in the environment

    International Nuclear Information System (INIS)

    Kudo, A.

    2001-01-01

    The first volume of the new series, Radioactivity in the Environment, focuses on the environmental occurrence, the speciation, the behaviour, the fate, the applications and the health consequences of that much-feared and much-publicised element, plutonium. Featuring a collection of selected, peer-reviewed, up-to-date papers by leading researchers in the field, this work provides a state-of-the-art description of plutonium in the environment. This title helps to explain where present frontiers are drawn in our continuing efforts to understand the science of environmental plutonium and will help to place widespread concerns into perspective. As a whole this new book series on environmental radioactivity addresses, at academic research level, the key aspects of this socially important and complex interdisciplinary subject. Presented objectively and with the ultimate authority gained from the many contributions by the world's leading experts, the negative and positive consequences of having a radioactive world around us will be documented and given perspective. refs