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Uranium trifluoride

Uranium trifluoride, which may be obtained by reduction of UF4 with H2 or by reaction of UF4 with UN at 95(FC is a high-melting, nonvolatile solid. It resembles the lanthanide trifluorides in being insoluble in water or dilute acids. [Pg.1146]

Its importance depends on the nuclear property of being readily fissionable with neutrons and its availability in quantity. The world s nuclear-power reactors are now producing about 20,000 kg of plutonium/yr. By 1982 it was estimated that about 300,000 kg had accumulated. The various nuclear applications of plutonium are well known. 238Pu has been used in the Apollo lunar missions to power seismic and other equipment on the lunar surface. As with neptunium and uranium, plutonium metal can be prepared by reduction of the trifluoride with alkaline-earth metals. [Pg.205]

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]

Fluorine reacts with the halogens and antimony to produce several compounds of commercial importance antimony pentafluoride [7783-70-2J, bromine trifluoride [7787-71 chlorine trifluoride [7790-91 -2J, and iodine pentafluoride [7783-66-6J. Chlorine trifluoride is used in the processing of UF (see Uraniumand uranium compounds). Bromine trifluoride is used in chemical cutting by the oil well industry (see Petroleum). Antimony and iodine pentafluorides are used as selective fluorinating agents to produce fluorochemical intermediates (see Fluorine compounds, inorganic). [Pg.131]

Aromatic amines form addition compounds and complexes with many inorganic substances, such as ziac chloride, copper chloride, uranium tetrachloride, or boron trifluoride. Various metals react with the amino group to form metal anilides and hydrochloric, sulfuric, or phosphoric acid salts of aniline are important intermediates in the dye industry. [Pg.229]

Fluorides. Uranium fluorides play an important role in the nuclear fuel cycle as well as in the production of uranium metal. The dark purple UF [13775-06-9] has been prepared by two different methods neither of which neither have been improved. The first involves a direct reaction of UF [10049-14-6] and uranium metal under elevated temperatures, while the second consists of the reduction of UF [10049-14-6] by UH [13598-56-6]. The local coordination environment of uranium in the trifluoride is pentacapped trigonal prismatic with an 11-coordinate uranium atom. The trifluoride is... [Pg.331]

Bismuth pentafluoride is an active fluorinating agent. It reacts explosively with water to form ozone, oxygen difluoride, and a voluminous chocolate-brown precipitate, possibly a hydrated bismuth(V) oxyfluoride. A similar brown precipitate is observed when the white soHd compound bismuth oxytrifluoride [66172-91 -6] BiOF, is hydrolyzed. Upon standing, the chocolate-brown precipitate slowly undergoes reduction to yield a white bismuth(Ill) compound. At room temperature BiF reacts vigorously with iodine or sulfur above 50°C it converts paraffin oil to fluorocarbons at 150°C it fluorinates uranium tetrafluoride to uranium pentafluoride and at 180°C it converts Br2 to bromine trifluoride, BrF, and bromine pentafluoride, BrF, and chlorine to chlorine fluoride, GIF. It apparently does not react with dry oxygen. [Pg.129]

Chlorine trifluoride is used to recover uranium from nuclear fuel rods in a high-temperature reaction that produces gaseous uranium hexafluoride 2 ClF3(g)+U( ) UF(5(g)-I-Cl2(g) Determine the Lewis... [Pg.594]

Johnson, K. etal., 6thNucl. Eng. Sci. Conf., New York, 1960. Reprint Paper No. 23 Uranium may ignite or explode during dissolution in bromine trifluoride, particularly when high concentrations of the hexafluoride are present. Causative factors are identified. [Pg.104]

Used industrially in the manufacture of fluorocarbons as a chemical intermediate in the manufacture of sulfur hexafluoride, chlorine trifluoride, bromine trifluoride uranium hexafluoride, molybdenum hexafluoride, perchloryl fluoride, and oxygen difluoride and as a rocket propellant. [Pg.333]

Fluorine is used in the separation of uranium, neptunium and plutonium isotopes by converting them into hexafluorides followed by gaseous diffusion then recovering these elements from nuclear reactors. It is used also as an oxidizer in rocket-fuel mixtures. Other applications are production of many fluo-ro compounds of commercial importance, such as sulfur hexafluoride, chlorine trifluoride and various fluorocarbons. [Pg.298]

Tungsten(VI) fluoride (WF6) and molybdenum(VI) fluoride (MoF6) are available commercially, and can be made by reaction of the metals with fluorine.4 In the case of uranium(VI) fluoride (UF6), a preparation that is claimed5 to be feasible in the laboratory uses uranium metal and chlorine trifluoride uranium(VI) fluoride is prepared6 commercially by the fluorination of uranium(IV) fluoride, itself prepared from an oxide and hydrogen fluoride. [Pg.679]

Preparation of fluorides aluminum trifluoride, uranium tetra- and hexafluorides... [Pg.577]

The UFg used in producing nuclear fuels is prepared by reaction of uranium metal with chlorine trifluoride. Tell which atoms have been oxidized and which reduced, and balance the equation. [Pg.228]

Phillips and Timms [599] described a less general method. They converted germanium and silicon in alloys into hydrides and further into chlorides by contact with gold trichloride. They performed GC on a column packed with 13% of silicone 702 on Celite with the use of a gas-density balance for detection. Juvet and Fischer [600] developed a special reactor coupled directly to the chromatographic column, in which they fluorinated metals in alloys, carbides, oxides, sulphides and salts. In these samples, they determined quantitatively uranium, sulphur, selenium, technetium, tungsten, molybdenum, rhenium, silicon, boron, osmium, vanadium, iridium and platinum as fluorides. They performed the analysis on a PTFE column packed with 15% of Kel-F oil No. 10 on Chromosorb T. Prior to analysis the column was conditioned with fluorine and chlorine trifluoride in order to remove moisture and reactive organic compounds. The thermal conductivity detector was equipped with nickel-coated filaments resistant to corrosion with metal fluorides. Fig. 5.34 illustrates the analysis of tungsten, rhenium and osmium fluorides by this method. [Pg.192]

Chlorine trifluoride, CIF3, is violently reactive with many oxidizable substrates. It is available commercially and has been utilized to fluormate uranium to UFe in the nuclear power industry. This is an important step in uranium enrichment because volatile UFe can be readily separated from the nonvolatile fluoride impurities. [Pg.1357]

After about 30 min the reaction ceases. At this stage the boron trifluoride and the excess boron trichloride must be removed. One way is to open valve 1 and pump them into the vacuum system (which should have a liquid-nitrogen scavenger trap). It is a considerable advantage of the preparative method that all the reagents and products, except uranium hexachloride, are volatile. [Pg.145]


See other pages where Uranium trifluoride is mentioned: [Pg.209]    [Pg.1738]    [Pg.1920]    [Pg.184]    [Pg.577]    [Pg.209]    [Pg.1738]    [Pg.1920]    [Pg.184]    [Pg.577]    [Pg.346]    [Pg.184]    [Pg.268]    [Pg.81]    [Pg.1917]    [Pg.346]    [Pg.869]    [Pg.6]    [Pg.679]    [Pg.632]    [Pg.129]    [Pg.2006]    [Pg.1917]    [Pg.383]    [Pg.648]    [Pg.77]    [Pg.1483]    [Pg.134]    [Pg.290]    [Pg.1001]    [Pg.1060]    [Pg.145]    [Pg.19]   
See also in sourсe #XX -- [ Pg.88 , Pg.89 ]

See also in sourсe #XX -- [ Pg.577 ]




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