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Uranium hexafluoride

Uranium hexafluoride is the key compound in the separation of the uranium isotopes and In its manufacture uranium(lV) oxide is first reacted with hydrogen fluoride to uranium tetrafluoride, which is then reacted with elemental fluorine to uranium hexalluoride  [Pg.142]

A detailed description of this process is given in Chapter 6. [Pg.142]


We also developed a number of other useful new fluorinating reagents. They ineluded a convenient in situ form of sulfur tetrafluoride in pyridinium polyhydrogen fluoride, selenium tetrafluoride, and ey-anurie fluoride. We introdueed uranium hexafluoride (UFg), depleted from the U-235 isotope, which is an abundant by-product of enrichment plants, as an effective fluorinating agent. [Pg.104]

Toluene Sulfuric plus nitric acids, nitrogen dioxide, silver perchlorate, uranium hexafluoride... [Pg.1212]

Fluorine was first produced commercially ca 50 years after its discovery. In the intervening period, fluorine chemistry was restricted to the development of various types of electrolytic cells on a laboratory scale. In World War 11, the demand for uranium hexafluoride [7783-81-5] UF, in the United States and United Kingdom, and chlorine trifluoride [7790-91 -2J, CIF, in Germany, led to the development of commercial fluorine-generating cells. The main use of fluorine in the 1990s is in the production of UF for the nuclear power industry (see Nuclearreactors). However, its use in the preparation of some specialty products and in the surface treatment of polymers is growing. [Pg.122]

Manufacturers. Besides manufacturers in the United States, commercial fluorine plants are operating in Canada, France, Germany, Italy, Japan, and the United Kingdom (see Table 5). Fluorine is also produced in the Commonwealth of Independent States (former Soviet Union) however, details regarding its manufacture, production volumes, etc, are regarded as secret information. The total commercial production capacity of fluorine in the United States and Canada is estimated at over 5000 t/yr, of which 70—80% is devoted to uranium hexafluoride production. Most of the gas is used in captive uranium-processing operations. [Pg.130]

Elemental fluorine is used captively by most manufacturers for the production of various inorganic fluorides (Table 5). The market for gaseous fluorine is small, but growing. The main use of fluorine is in the manufacture of uranium hexafluoride, UF, by... [Pg.131]

Uranium hexafluoride is used in the gaseous diffusion process for the separation and enrichment of uranium-235, which exists in low concentration in natural uranium. The enriched UF is converted back into an oxide and used as fuel for the nuclear power industry. [Pg.131]

Chlorine ttifluoride is utilized in the processing of nuclear fuels to convert uranium to gaseous uranium hexafluoride. Chlorine ttifluoride has also been used as a low temperature etchant for single-crystalline siHcon (122,123). [Pg.187]

The raw material for nuclear reactor fuel, uranium, exits the mining—milling sequence as uranium oxide. Because of its color, it is called yellow cake. The yellow cake is converted to uranium hexafluoride and enriched in 235u... [Pg.201]

Uranium oxide [1344-57-6] from mills is converted into uranium hexafluoride [7783-81-5] FJF, for use in gaseous diffusion isotope separation plants (see Diffusion separation methods). The wastes from these operations are only slightly radioactive. Both uranium-235 and uranium-238 have long half-Hves, 7.08 x 10 and 4.46 x 10 yr, respectively. Uranium enriched to around 3 wt % is shipped to a reactor fuel fabrication plant (see Nuclear REACTORS, NUCLEAR FUEL reserves). There conversion to uranium dioxide is foUowed by peUet formation, sintering, and placement in tubes to form fuel rods. The rods are put in bundles to form fuel assembHes. Despite active recycling (qv), some low activity wastes are produced. [Pg.228]

In TBP extraction, the yeUowcake is dissolved ia nitric acid and extracted with tributyl phosphate ia a kerosene or hexane diluent. The uranyl ion forms the mixed complex U02(N02)2(TBP)2 which is extracted iato the diluent. The purified uranium is then back-extracted iato nitric acid or water, and concentrated. The uranyl nitrate solution is evaporated to uranyl nitrate hexahydrate [13520-83-7], U02(N02)2 6H20. The uranyl nitrate hexahydrate is dehydrated and denitrated duting a pyrolysis step to form uranium trioxide [1344-58-7], UO, as shown ia equation 10. The pyrolysis is most often carried out ia either a batch reactor (Fig. 2) or a fluidized-bed denitrator (Fig. 3). The UO is reduced with hydrogen to uranium dioxide [1344-57-6], UO2 (eq. 11), and converted to uranium tetrafluoride [10049-14-6], UF, with HF at elevated temperatures (eq. 12). The UF can be either reduced to uranium metal or fluotinated to uranium hexafluoride [7783-81-5], UF, for isotope enrichment. The chemistry and operating conditions of the TBP refining process, and conversion to UO, UO2, and ultimately UF have been discussed ia detail (40). [Pg.318]

Uranium hexafluoride [7783-81-5], UF, is an extremely corrosive, colorless, crystalline soHd, which sublimes with ease at room temperature and atmospheric pressure. The complex can be obtained by multiple routes, ie, fluorination of UF [10049-14-6] with F2, oxidation of UF with O2, or fluorination of UO [1344-58-7] by F2. The hexafluoride is monomeric in nature having an octahedral geometry. UF is soluble in H2O, CCl and other chlorinated hydrocarbons, is insoluble in CS2, and decomposes in alcohols and ethers. The importance of UF in isotopic enrichment and the subsequent apphcations of uranium metal cannot be overstated. The U.S. government has approximately 500,000 t of UF stockpiled for enrichment or quick conversion into nuclear weapons had the need arisen (57). With the change in pohtical tides and the downsizing of the nation s nuclear arsenal, debates over releasing the stockpiles for use in the production of fuel for civiUan nuclear reactors continue. [Pg.332]

Bismuth Penta.fIuoride, Bismuth(V) fluoride consists of long white needles that have been shown to have the same stmcture as the body-centered, tetragonal a-polymorph of uranium hexafluoride. The density of the soHd is 5.4 g/mL at 25°C. The soHd consists of infinite chains of trans-bridged BiF polyhedra dimers and trimers are present in the vapor phase (22). Bismuth pentafluoride may be prepared by the fluorination of BiF or... [Pg.129]

Figure 7 is a schematic representation of a section of a cascade. The feed stream to a stage consists of the depleted stream from the stage above and the enriched stream from the stage below. This mixture is first compressed and then cooled so that it enters the diffusion chamber at some predetermined optimum temperature and pressure. In the case of uranium isotope separation the process gas is uranium hexafluoride [7783-81-5] UF. Within the diffusion chamber the gas flows along a porous membrane or diffusion barrier. Approximately one-half of the gas passes through the barrier into a region... [Pg.84]

Fluorine. Fluorine is the most reactive product of all electrochemical processes (63). It was first prepared in 1886, but important quantities of fluorine were not produced until the early 1940s. Fluorine was required for the production of uranium hexafluoride [7783-81 -5] UF, necessary for the enrichment of U (see DIFFUSION SEPARATION METHODS). The Manhattan Project in the United States and the Tube Alloy project in England contained parallel developments of electrolytic cells for fluorine production (63). The principal use of fluorine continues to be the production of UF from UF. ... [Pg.78]

Polychlorotrifluoroethylene was the first fluorinated polymer to be produced on an experimental scale and polymers were used in Germany and in the United States early in World War II. PCTFE was used, in particular, in connection with the atomic bomb project in the handling of corrosive materials such as uranium hexafluoride. [Pg.374]

URANIUM HEXAFLUORIDE URANYL ACETATE URANYL NITRATE URANYL NITRATE HEXAHYDRATE... [Pg.252]

Canada, are examples. These reactors do not use ordinai y water for the moderator. Most nuclear fission reactors use ordinaiy water for a moderator which requires that the fuel he about 3 percent and about 97 percent U. Achieving this enrichment requires that the solid uranium compounds in the yellow cake be converted to gaseous uranium hexafluoride (UF,). Following enrichment, gaseous UF is converted to solid uranium oxide (UO,) for fabrication of fuel elements for a nuclear reactor. [Pg.863]

Nuclear power is now the only substantial use for uranium. But before uranium can be used in a nuclear reactor, it must undergo several processes. After uranium is mined from geological mineral deposits, it is purified and converted into uranium hexafluoride (UF,). The UF, is next enriched, increasing the concentration of U-235 by separating out UF,5 made with U-238 atoms. The enriched UF, is then converted into uranium dioxide (UO,), and pressed into fuel pellets for use in the nuclear reactor. [Pg.866]

During the conversion process, the object is to create uranium hexafluoride (UF ), a highly corro-sh e substance that is gaseous at high temperatures, but is a white crystalline solid at lower temperatures. Uranium hexafluoride is easily transported in its ciystalline form to an enrichment facility (the step taken after conversion), but the gaseous form is well suited for the enrichment process, itself. First, the... [Pg.868]

At what temperature will a molecule of uranium hexafluoride, the densest gas known, have the same average speed as a molecule of the lightest gas, hydrogen, at 37°C ... [Pg.129]

A compound of chlorine and fluorine, CIF, reacts at about 75°C with uranium to produce uranium hexafluoride and chlorine fluoride, C1F. A certain amount of uranium produced 5.63 g of uranium hexafluoride and 457 mL of chlorine fluoride at 75°C and 3.00 atm. What is x Describe foe geometry, polarity, and bond angles of foe compound and foe hybridization of chlorine. How many sigma and pi bonds are there ... [Pg.195]

Our discussion concentrates on the uranium-235 isotope. It makes up only about 0.7% of naturally occurring uranium. The more abundant isotope, uranium-238, does not undergo fission. The first process used to separate these isotopes, and until recently the only one available, was that of gaseous effusion (Chapter 5). The volatile compound uranium hexafluoride, UF6, which sublimes at 56°C, is used for this purpose. [Pg.524]

Caseous uranium hexafluoride is important in the preparation of uranium as a source of atomic energy. ... [Pg.35]

What is the ratio of the weight of one uranium hexafluoride molecule to the weight of an oxygen molecule State any guiding principles needed in answering this question. [Pg.35]

Unsaturated, hydrocarbons, 342 Uranium compounds, 223 electron configuration, 415 oxidation number, 414 preparation, 35 Uranium hexafluoride, 35 Uranus, data on, 444 Urea, 434... [Pg.466]


See other pages where Uranium hexafluoride is mentioned: [Pg.346]    [Pg.298]    [Pg.528]    [Pg.689]    [Pg.1040]    [Pg.1040]    [Pg.190]    [Pg.199]    [Pg.252]    [Pg.198]    [Pg.201]    [Pg.202]    [Pg.297]    [Pg.415]    [Pg.323]    [Pg.323]    [Pg.96]    [Pg.104]    [Pg.496]    [Pg.40]    [Pg.1]    [Pg.552]    [Pg.268]    [Pg.202]    [Pg.121]   
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Hexafluoride

Hexafluorides

Isotopic Analysis of Uranium Hexafluoride

Requirements for packages containing uranium hexafluoride

Sampling of Uranium Hexafluoride

Uranium Hexafluoride UF

Uranium Hexafluoride and Isotope Separation

Uranium Hexafluoride in Pressurized Cylinders

Uranium hexafluoride isotope separation using

Uranium hexafluoride porous membrane

Uranium hexafluoride production

Uranium hexafluoride properties

Uranium hexafluoride synthesis

Uranium hexafluoride, crystal

Uranium hexafluoride, vapor pressure

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