Oxidation uranium oxides

Although the logistic problems involved with rl8 000 fuel pieces and 600 000 pieces of depleted uranium, canned sodium, Iron oxide, uranium oxide, etc., are significant, extension of many years experience with the smaller facility Zero Power Reactor 3 (ZPR-3) indicates that safe and efficient operation of ZPPR can be achieved. 

J. D. CHALMERS, Criticality Parameters for Mixtures of Plutonium Oxide, Uranium Oxide and Water, Criticality Control of Fissile Material, pp. 3-11, International Atomic Energy Agency, Vienna (1966). 

Criticality Safety Considerations in the Design of a Large Concrete Storage Array for Plutonium Oxide-Uranium Oxide Fuel Sub-assemblies, C. L. Brown, L, C. Davenport (PNL), ... 

C968. (2012). Test methods for analysis of sintered gadolinium oxide-uranium oxide pellets. West Conshohocken, PA ASTM. 

Reaction Rates of Stoichiometric H2-O2 Mixtures IN Thorium Oxide-Uranium Oxide Slurries... 

The second generation Sohio catalyst, introduced during the inid-l%0s, was an antimony oxide/uranium oxide mixture (U03-2Sb203). A successful iron oxide/antimony oxide catalyst containing some tellurium oxide was subsequently developed by Nitto, a Sohio licensee, in Japan. ... 

The larger cations of Group 1 (K, Rb, Cs) can be precipitated from aqueous solution as white solids by addition of the reagent sodium tetraphenylborate, NaB(C( H5)4. Sodium can be precipitated as the yellow sodium zinc uranium oxide ethanoate (sodium zinc uranyl acetate). NaZn(U02)3(CH3C00)y. 9H2O. by adding a clear solution of zinc uranyl acetate in dilute ethanoic acid to a solution of a sodium salt. 

The many possible oxidation states of the actinides up to americium make the chemistry of their compounds rather extensive and complicated. Taking plutonium as an example, it exhibits oxidation states of -E 3, -E 4, +5 and -E 6, four being the most stable oxidation state. These states are all known in solution, for example Pu" as Pu ", and Pu as PuOj. PuOl" is analogous to UO , which is the stable uranium ion in solution. Each oxidation state is characterised by a different colour, for example PuOj is pink, but change of oxidation state and disproportionation can occur very readily between the various states. The chemistry in solution is also complicated by the ease of complex formation. However, plutonium can also form compounds such as oxides, carbides, nitrides and anhydrous halides which do not involve reactions in solution. Hence for example, it forms a violet fluoride, PuFj. and a brown fluoride. Pup4 a monoxide, PuO (probably an interstitial compound), and a stable dioxide, PUO2. The dioxide was the first compound of an artificial element to be separated in a weighable amount and the first to be identified by X-ray diffraction methods. 

Planet Uranus) Yellow-colored glass, containing more than 1% uranium oxide and dating back to 79 A.D., has been found near Naples, Italy. Klaproth recognized an unknown element in pitchblende and attempted to isolate the metal in 1789. 

Uranium can be prepared by reducing uranium halides with alkali or alkaline earth metals or by reducing uranium oxides by calcium, aluminum, or carbon at high temperatures. The metal can also be produced by electrolysis of KUF5 or UF4, dissolved in a molten mixture of CaCl2 and NaCl. High-purity uranium can be prepared by the thermal decomposition of uranium halides on a hot filament. 

Although acrylonitrile manufacture from propylene and ammonia was first patented in 1949 (30), it was not until 1959, when Sohio developed a catalyst capable of producing acrylonitrile with high selectivity, that commercial manufacture from propylene became economically viable (1). Production improvements over the past 30 years have stemmed largely from development of several generations of increasingly more efficient catalysts. These catalysts are multicomponent mixed metal oxides mostly based on bismuth—molybdenum oxide. Other types of catalysts that have been used commercially are based on iron—antimony oxide, uranium—antimony oxide, and tellurium-molybdenum oxide. 

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. 

The balance of hydrogen fluoride is used ia appHcations such as stainless steel pickling inorganic fluoride production, alkylation (qv), uranium enrichment, and fluorine production. Hydrogen fluoride is used to convert uranium oxide to UF which then reacts with elemental fluorine to produce volatile UF. ... 

CoF is used for the replacement of hydrogen with fluorine in halocarbons (5) for fluorination of xylylalkanes, used in vapor-phase soldering fluxes (6) formation of dibutyl decalins (7) fluorination of alkynes (8) synthesis of unsaturated or partially fluorinated compounds (9—11) and conversion of aromatic compounds to perfluorocycHc compounds (see Fluorine compounds, organic). CoF rarely causes polymerization of hydrocarbons. CoF is also used for the conversion of metal oxides to higher valency metal fluorides, eg, in the assay of uranium ore (12). It is also used in the manufacture of nitrogen fluoride, NF, from ammonia (13). 

To convert naturally occurring uranium oxide, yellow cake or U Og, to the gaseous UF, hydrofluoric acid is first used to convert the U Og to UF. Further fluorination using fluorine (generated from more HF) is employed to convert the UF to UF. The UF is then processed at gaseous diffusion enrichment plants. 

Dioxygea difluoride has fouad some appHcatioa ia the coaversioa of uranium oxides to UF (66), ia fluoriaatioa of actinide fluorides and oxyfluorides to AcF (67), and in the recovery of actinides from nuclear wastes (68) (see Actinides and transactinides Nuclear reaction, waste managel nt). 

The heavy mineral sand concentrates are scmbbed to remove any surface coatings, dried, and separated into magnetic and nonmagnetic fractions (see Separation, magnetic). Each of these fractions is further spHt into conducting and nonconducting fractions in an electrostatic separator to yield individual concentrates of ilmenite, leucoxene, monazite, mtile, xenotime, and zircon. Commercially pure zircon sand typically contains 64% zirconium oxide, 34% siUcon oxide, 1.2% hafnium oxide, and 0.8% other oxides including aluminum, iron, titanium, yttrium, lanthanides, uranium, thorium, phosphoms, scandium, and calcium. 

The abihty of magnesium metal to reduce oxides of other metals can be exploited to produce metals such as zirconium, titanium [7440-32-6] and uranium [7440-61-1] (see ZiRCONiUMAND ZIRCONIUM COMPOUNDS Titaniumand titanium alloys Uraniumand uranium compounds). These reactions are... 

Ura.nium, The hydrometallurgical treatment of uranium ores is a concentration and purification process. Typical ore grade is 0.1—0.5% U Og, and pregnant solutions contain ca 1 kg/m of U Og. The dissolution requires the presence of an oxidant, either oxygen or a ferric salt. 

Nuclear Applications. Use of the nitrides of uranium-235 and thorium as fuels and breeders in high temperature reactors has been proposed (see Nuclearreactors). However, the compounds most frequently used for this purpose are the oxides and carbides. Nitrides could be useful in high... 

Geochemical Nature and Types of Deposits. The cmst of the earth contains approximately 2—3 ppm uranium. AlkaHc igneous rock tends to be more uraniferous than basic and ferromagnesian igneous rocks (10). Elemental uranium oxidizes readily. The solubiHty and distribution of uranium in rocks and ore deposits depend primarily on valence state. The hexavalent uranium ion is highly soluble, the tetravalent ion relatively insoluble. Uraninite, the most common mineral in uranium deposits, contains the tetravalent ion (II). 

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... 

By contrast, uranium fuels for lightwater reactors fall between these extremes. A typical pressurized water reactor (PWR) fuel element begins life at an enrichment of about 3.2% and is discharged at a bum-up of about 30 x 10 MW-d/t, at which time it contains about 0.8 wt % and about 1.0 wt % total plutonium. Boiling water reactor (BWR) fuel is lower in both initial enrichment and bum-up. The uranium in LWR fuel is present as oxide pellets, clad in zirconium alloy tubes about 4.6 m long. The tubes are assembled in arrays that are held in place by spacers and end-fittings. 

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