A preliminary chemical flowsheet is presented of a fluoride volatility process for recovering and decontaminating uranium from heterogeneous reactor fuels after dissolution in a fused salt. In laboratory work, a gross β decontamination factor of > 10 4 was obtained in the fluorination of a UF4-NaF-ZrF4 melt by passing the product UF6 through NaF at 650°C. The solubility of UF6 in molten NaF-ZrF4 was shown in kinetic studies to cause a lag in the evolution of UF6 from the fluorinator. Corrosion of nickel in the fluorination step appeared to be 2-4 mils/hr during the time that uranium was present. The average corrosion rate over the process as a whole was less than O.4 mil/hr. Earlier studies were reported in ORNL-1709 and 1877.

A summary of the laboratory development program on aqueous uranium slurry fuels for the Homogenous Reactor Project during the period April 1951 through March 1953 is presented. These investigations were devoted primarily to a study of the uranium oxides in aqueous suspensions. It was concluded that U(VI) was most likely to be the stable valence state in such slurry fuels and it was shown that β-UO3·H2O platelet crystals were the stable modification at 250°C. Very pure slurries of β-UO3·H2O platelets, uranium concentration of 250g/liter and average particle size of about 10 μ, had favorable settling rates and could be easily redispersed. Their viscosity and corrosion rate in stainless steel were comparable with those in water. Exposure of these slurries to pile radiation disclosed that radiolytic hydrogen and oxygen gas pressure comparable in magnitude to those of uncatalyzed uranyl sulfate solutions could be expected. Fission products in the irradiated slurries were predominantly associated with the solids. Radiation also tended to promote caking of these solids on the walls of the radiation bombs. Uranyl phosphate and the magnesium uranates were briefly investigated as alternate system but were not found satisfactory. The program was discontinued before the feasibility of uranium slurries for reactor …

Construction of the HRT reactor shield tank was completed, and the inside surfaces were painted. The roof structure for the tank is being assembled in preparation for an acceptance pressure test. Service piping and instrument lines are being installed in the central room area by ORNL craft forces. This work is approximately 50% complete. Fabrication of all temperature system components, except the blanket outer storage tanks, has been completed.

An ion-exchange -- polarographic method was developed for the determination of iron(III) in Homogeneous Reactor Fuels. Copper, which interferes, is removed from the fuel by plating it onto a cadmium coil. Iron is oxidized to iron(III) by potassium permanganate, and the iron(III) is separated from interfering metal ions by ion exchange on a Dowex 1 resin column that is in the sulfate form. The iron(III) in the effluent is determined polarographically in 0.5 M sodium citrate solution as supporting electrolyte. A fairly well defined polarographic wave is obtained for the iron(III) → iron(II) reduction at a half-wave potential of approximately -0.15 v. vs. the S.C.E. The relative standard deviation of the data for 2 µg of iron(III) per ml of solution in the polarographic cell was 6.5%; for 10 µg of iron(III) per ml it was 0.6%.