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Plutonium processing addition

When neutrons strike the nucleus of a large atom, they cause that nucleus to split apart into two roughly equal pieces known as fission products. In that process, additional neutrons and very large amounts of energy are also released. Only three isotopes are known to be fissionable, uranium-235, uranium-233, and plutonium-239. Of these, only the first, uranium-235, occurs naturally. Pluto-nium-239 is produced synthetically when nuclei of uranium-238 are struck by neutrons and transformed into plutonium. Since uranium-238 always occurs along with uranium-235 in a nuclear reactor, plutonium-239 is produced as a byproduct in all commercial reactors now in operation. As a result, it has become as important in the production of nuclear power as uranium-235. Uranium-233 can also be produced synthetically by the bombardment of thorium with neutrons. Thus far, however, this isotope has not been put to practical use in nuclear reactors. [Pg.597]

Ions of different valences of a metal behave like different elements with respect to extract-ability. The difference between Ce and Ce in Table 4.2 is one example. Another is afforded by Pu and Pu 02, which are readily extracted by TBP in kerosene, whereas Pu has a very low distribution coefficient [G31. Consequently, by adjusting the oxidation-reduction potential of the aqueous phase to control the proportion of an element in different valence states, it is possible to vary its distribution coefficient between wide limits. This is the mearts by which plutonium is stripped from aqueous solutions containing plutonium and uranium in sections C and D of Fig. 4.5 illustrating the Purex process. Addition of a reducing... [Pg.165]

These variations permit the separation of other components, if desired. Additional data on uranium, plutonium, and nitric acid distribution coefficients as a function of TBP concentration, solvent saturation, and salting strength are available (24,25). Algorithms have also been developed for the prediction of fission product distributions in the PUREX process (23). [Pg.205]

Preparation of Plutonium Metal from Fluorides. Plutonium fluoride, PuF or PuF, is reduced to the metal with calcium (31). Although the reactions of Ca with both fluorides are exothermic, iodine is added to provide additional heat. The thermodynamics of the process have been described (133). The purity of production-grade Pu metal by this method is ca 99.87 wt % (134). Metal of greater than 99.99 wt % purity can be produced by electrorefining, which is appHcable for Pu alloys as well as to purify Pu metal. The electrorefining has been conducted at 740°C in a NaCl—KCl electrolyte containing PuCl [13569-62-5], PuF, or PuF. Processing was done routinely on a 4-kg Pu batch basis (135). [Pg.201]

Plutonium Scrap Processing. In addition to recovering plutonium from irradiated reactor fuel, a Plutonium Reclamation Facility (PRF)( 7,8) is operated at the Hanford site to recover, separate, and purTfy kilogram amounts of plutonium from a wide range of unirradiated scrap materials. A 20 percent TBP-CC1 k solution is used to extract Pu(IV) from HN03-HF-A1(N03)3 solutions of dissolved scrap. [Pg.351]

In addition to fuel and targets(15J6) from SRP reactors, SRP also reprocesses a wide variety of fuels from offsite research reactors and a wide range of unirradiated plutonium scrap materials.(17) Following customary Savannah River practice, initial processing of each offsite material is designed to transform the actinides to a solution that is compatible with one of the solvent extraction cycles in either of the separations areas. A major advantage of this practice is that the... [Pg.354]

In addition, some plutonium is also lost to the salt as PuCl3. A two-step counter-current extraction is used to minimize the amount of salt used in the MSE process, reduce plutonium losses... [Pg.366]

The electrolyte salt must be processed to recover the ionic plutonium orginally added to the cell. This can be done by aqueous chemistry, typically by dissolution in a dilute sodium hydroxide solution with recovery of the contained plutonium as Pu(OH)3, or by pyrochemical techniques. The usual pyrochemical method is to contact the molten electrolyte salt with molten calcium, thereby reducing any PUCI3 to plutonium metal which is immiscible in the salt phase. The extraction crucible is maintained above the melting point of the contained salts to permit any fine droplets of plutonium in the salt to coalesce with the pool of metal formed beneath the salt phase. If the original ER electrolyte salt was eutectic NaCl-KCl a third "black salt" phase will be formed between the stripped electrolyte salt and the solidified metal button. This dark-blue phase can contain 10 wt. % of the plutonium originally present in the electrolyte salt plutonium in this phase can be recovered by an additional calcium extraction stepO ). [Pg.401]

In addition, we are evaluating problems in the areas of process and equipment design have been evaluated. Most recent efforts are concerned with the recovery and recycle of plutonium values in the residues. [Pg.406]

Process Schematic. A schematic showing our main production sequence and residue recyle streams is seen in Figure 11. In addition on this figure, (shown in the pentagonal shaped boxes) are two proposed plutonium recycle streams which are under investigation but are not being used in the production sequence. [Pg.419]

Conceptual Flowsheet for the Extraction of Actinides from HLLW. Figure 5 shows a conceptual flowsheet for the extraction of all the actinides (U, Np, Pu, Am, and Cm) from HLLW using 0.4 M 0< >D[IB]CMP0 in DEB. The CMPO compound was selected for this process because of the high D m values attainable with a small concentration of extractant and because of the absence of macro-concentrations of uranyl ion. Distribution ratios relevant to the flowsheet are shown in previous tables, IV, V, VI, and VII and figures 1 and 2. One of the key features of the flowsheet is that plutonium is extracted from the feed solution and stripped from the organic phase without the addition of any nitric acid or use of ferrous sulfamate. However, oxalic acid is added to complex Zr and Mo (see Table IV). The presence of oxalic acid reduces any Np(VI) to Np(IV) (15). The presence of ferrous ion, which is... [Pg.439]

Workers at plutonium reprocessing facilities, nuclear reactors, transuranium and low level waste storage facilities, or those engaged in the production or processing of243Am or241 Am may be occupationally exposed to americium. In addition, workers at sites where nuclear testing was conducted may also be exposed to americium. Workers in nuclear power stations may be exposed to airborne radionuclides. The... [Pg.190]

Figure 12.5 illustrates the basic components of the Purex process three purification cycles for both uranium and plutonium are shown. High levels of beta and gamma radioactivity are present only in the first cycle, in which 99.9% of the fission products are separated. The other two cycles, based upon the same chemical reactions as the first cycle, obtain additional decontamination and overall purity of the uranium and plutonium products. [Pg.520]

Einsteinium does not exist in nature and is not found in the Earth s crust. It is produced in small amounts by artificial nuclear transmutations of other radioactive elements rather than by additional explosions of thermonuclear weapons. The formation of einsteinium from decay processes of other radioactive elements starts with plutonium and proceeds in five steps as follows ... [Pg.329]

One of the fascinating features of fission power is the breeding of fission fuel from nonfissionable uranium-238. Breeding occurs when small amounts of fissionable isotopes are mixed with uranium-238 in a reactor. Fission liberates neutrons that convert the relatively abundant nonfissionable uranium-238 to uranium-239, which beta-decays to neptunium-239, which in turn beta-decays to fissionable plutonium-239. So in addition to the abundant energy produced, fission fuel is bred from relatively abundant uranium-238 in the process. [Pg.129]

When the fuel is initially loaded into die reactor, the core region will typically contain from 10 to 15% fissile isotopes with the remainder being ijSU. Essentially all of the blanket will be 238U. As energy is extracted from the fissile isotopes, they become depleted (the initial plutonium is gradually used up), However, in a breeder reactor, new plutonium will be formed in die cure and blanket regions faster Ilian it is consumed. Additionally, undesirable fission products are formed which must ultimately be removed. This process is schematically illustrated in Fig. 31. The before chart... [Pg.1117]

In tlie PUREX process, the spent fuel and blanket materials are dissolved in nitric acid to form nitrates of plutonium and uranium. These are separated chemically from the other fission products, including the highly radioactive actinides, and then the two nitrates are separated into tv/o streams of partially purified plutonium and uranium. Additional processing will yield whatever purity of the two elements is desired. The process yields purified plutonium, purified uranium, and high-level wastes. See also Radioactive Wastes in the entry1 on Nuclear Power Technology. Because of the yield of purified plutonium, the PUREX process is most undesirable from a nuclear weapons proliferation standpoint,... [Pg.1647]


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