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Uranium electrolytic

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]

Metalliding. MetaUiding, a General Electric Company process (9), is a high temperature electrolytic technique in which an anode and a cathode are suspended in a molten fluoride salt bath. As a direct current is passed from the anode to the cathode, the anode material diffuses into the surface of the cathode, which produces a uniform, pore-free alloy rather than the typical plate usually associated with electrolytic processes. The process is called metalliding because it encompasses the interaction, mostly in the soHd state, of many metals and metalloids ranging from beryUium to uranium. It is operated at 500—1200°C in an inert atmosphere and a metal vessel the coulombic yields are usually quantitative, and processing times are short controUed... [Pg.47]

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]

Excer A process for making uranium tetrafluoride by electrolytic reduction of a uranyl fluoride solution, precipitation of a uranium tetrafluoride hydrate, and ignition of this. [Pg.103]

Lead hydroxide is used in making porous glass in electrical-insulating paper in electrolytes in sealed nickel-cadmium batteries in recovery of uranium from seawater and as a catalyst for oxidation of cyclododecanol. [Pg.471]

U(III) species and a second three-electron reduction to give U(0) metal. The first reduction, U(IV)/U(III) couple, is elec-trochemically and chemically irreversible except in hexamethylphosphoramide at 298 K where the authors report full chemical reversibility on the voltammetric timescale. The second reduction process is electrochemically irreversible in all solvents and only in dimethylsulfone at 400 K was an anodic return wave associated with uranium metal stripping noted. Electrodeposition of uranium metal as small dendrites from CS2UCI6 starting material was achieved from molten dimethylsulfone at 400 K with 0.1 M LiCl as supporting electrolyte at a platinum cathode. The deposits of uranium and the absence of U CI3, UCI4, UO2, and UO3 were determined by X-ray diffraction. Faradaic yield was low at 17.8%, but the yield can be increased (55.7%) through use of a mercury pool cathode. [Pg.1066]

Fluorine compounds from fluorite (fluorspar, CaF2) are used in water treatment (to suppress dental caries) and to make fluoropolymers (such as Teflon), lubricants, and refrigerants. Molten cryolite (Na3AlF6) is essential as a solvent for Al203 in the electrolytic production of aluminum metal, while the isotopic enrichment of uranium for nuclear power reactors is usually achieved by diffusion or gas centrifugation of volatile UF6. [Pg.7]

The electrolysis of P-diketone solutions in ethanol (0.4-0.6 M) was carried out using a uranium anode and nickel cathode for 3-5 hr at 45-60 mA in an inert atmosphere (Ar, He) as in an oxidative one (02, dry air) with agitation. LiCl was used as supporting electrolyte (O.lmol/L). P-Diketones [acetylacetone (Hacac) and benzoylacetone (Hba)] were distilled before use. [Pg.269]


See other pages where Uranium electrolytic is mentioned: [Pg.318]    [Pg.69]    [Pg.323]    [Pg.133]    [Pg.337]    [Pg.324]    [Pg.332]    [Pg.399]    [Pg.1277]    [Pg.106]    [Pg.332]    [Pg.62]    [Pg.624]    [Pg.147]    [Pg.466]    [Pg.366]    [Pg.64]    [Pg.1055]    [Pg.1056]    [Pg.1058]    [Pg.1059]    [Pg.1061]    [Pg.1063]    [Pg.1064]    [Pg.362]    [Pg.13]    [Pg.1139]    [Pg.1139]    [Pg.1139]    [Pg.399]    [Pg.30]    [Pg.1457]    [Pg.759]    [Pg.940]    [Pg.88]    [Pg.62]    [Pg.341]    [Pg.180]    [Pg.324]   
See also in sourсe #XX -- [ Pg.340 ]




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