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Uranium placement

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]

Several application methods are available for enzymatic reduction and precipitation of uranium. These include bioreactors, placement of the microorganisms on solid substrates for filtration, or placement in groundwater to create precipitation zones through which the contaminated groundwater migrates. [Pg.1085]

Neutron multiplying parameters for large SP placement spacing had been studied using RITM reactor code, in which the neutron transfer equation is solved by the method of successive collisions. The composition of the canister (R=ll cm) fuel zone is represented by the uranium-zirconium SNF with enrichment of 56.7% by... [Pg.284]

Fig. 1.3 Setup for first chemical experiments with element 104 - now Rf Dubna, the mid-1960s [10]. The broken frames outline the placement of resistive heaters, paraffin and cadmium shielded the detectors from neutrons to prevent induced fission of uranium impurities in mica. Thermal decomposition of NaNbClg was the source of NbC E vapor. A Faraday cup was placed inside the target chamber (not shown). Fig. 1.3 Setup for first chemical experiments with element 104 - now Rf Dubna, the mid-1960s [10]. The broken frames outline the placement of resistive heaters, paraffin and cadmium shielded the detectors from neutrons to prevent induced fission of uranium impurities in mica. Thermal decomposition of NaNbClg was the source of NbC E vapor. A Faraday cup was placed inside the target chamber (not shown).
Vasudevan and co-workers reported the development of a photochemical microfluidic device which was fabricated from stainless steel. They devised a method of sealing the channels with an FEP membrane, a UV transparent fluoropolymer, which was compressed to the stainless steel channel utilizing a pressurized nitrogen chamber with a quartz window. The device had a total reaction volume of 980 uL (width = 1000 pm, depth = 250 pm, length = 3930 pm), was irradiated by placement in front of a medium pressure Hg arc lamp, and wavelength was controlled by inserting a uranium doped quartz panel into the window. [Pg.178]


See other pages where Uranium placement is mentioned: [Pg.786]    [Pg.331]    [Pg.978]    [Pg.288]    [Pg.151]    [Pg.11]    [Pg.22]    [Pg.24]    [Pg.1774]    [Pg.190]    [Pg.967]    [Pg.887]    [Pg.63]    [Pg.342]    [Pg.174]    [Pg.47]    [Pg.32]    [Pg.6]    [Pg.129]    [Pg.887]   
See also in sourсe #XX -- [ Pg.110 , Pg.304 ]




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