The development of the reactor layout is continuing. New features that have been incorporated because of stress, fluid flow, or fabricability considerations include an elliptical fuel expansion tank, a rounded dome to enclose the top of the reactor, a newly designed sodium pump impeller, and other related items. Recently completed heat exchanger tests yielded consistent data from which a series of heat exchangers is being designed. The most promising of these will be chosen for the ART.

The successful completion of a program of experiments, including the Aircraft Reactor Experiment (ARE), has demonstrated the high probability of producing militarily useful aircraft nuclear power plants employing reflector-moderated circulating-fuel reactors. Consequently, and accelerated program culminating in operation of the Aircraft Reactor Test (ART) is under way. In order to adhere to the compressed schedule of the accelerated program, it is essential that the Atomic Energy Commission approve the 7500 Area in Oak Ridge as the test site by February15, 1955. This report summarizes the hazards associated with operating the contained 60-Mv reactor of the ART at the proposed Oak Ridge test site.

The development of ionic methods for the determination of corrosion products in the highly radioactive Homogeneous Reactor (HR) fuels has been of major interest in the work of the Ionic Analyses Laboratory. Methods for the spectrophotometric determination of aluminum and for the polarographic determination of iron in HR fuels have been developed. The polarographic determination of molybdenum in uranyl sulfate solutions was studied. A polarographic method for the determination of zinc was developed. A fluorometric method for the determination of microgram amounts of fluoride was studied. Three organic reagents were investigated as precipitants for microgram quantities of zirconium in HR fuel. The automatic photometric titration technique was applied to the determination of thorium and of sulfate. A method was developed for the ionexchange separation and potentiometric titration of cobalt. The ultraviolet absorption spectra of technetium and rhenium were studied.

The development of ionic methods for the determination of corrosive products in the highly radioactive Homogeneous Reactor (HR) fuels has been of major interest in the work of the Ionic Analyses Laboratory. Methods for the spectrophotometric determination of aluminum and for the polarographic determination of iron in HR fuels have been developed. The polarographic determination of molybdenum in uranyl sulfate solutions was studied. A polarographic method for the determination of zinc was developed. A fluorometric method for the determination of microgram amounts of fluoride was studied. Three organic reagents were investigated as precipitants for microgram quantities of zirconium in HR fuel. The automatic photometric titration technique was applied to the determination of thorium and of sulfate. A method was developed for the ion-exchange separation and potentiometric titration of cobalt. The ultraviolet absorption spectra of technetium and rhenium were studied.

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 …

Progress report of the Oak Ridge National Laboratory Biology Division providing updates on various projects, experiments, and other work. This report includes a summary of scholarly output from the division and departmental activities in: cytology and genetics, microbial protection and recovery, mammalian recovery, mammalian genetics and development, pathology and physiology, microbiology, biochemistry, enzymology and photosynthesis, plant biochemistry, general physiology, and biophysics.

New systems involving the exchange of boron between boron trifluoride and boron trifluoride addition compounds have been explored. These systems have large separation factors and potentially simple reflux mechanisms. A precise determination of this separation factor for the anisole-boron trifluoride system gave the value (see report). Boron exchange was found to occur between BF and BCl3. Several homogenous catalysts have been found which activate the hydrogen-water exchange, but none are adoptable to the production of deuterium because of the slow exchange rate. Platinum or platinum oxide may be usable as a heterogeneous catalyst with proper support or dispersion techniques. The high-pressure solubility of hydrogen in several amalgams was investigated in connection with a unique countercurrent exchange system. A proposed system involving isotopic exchange between lithium dipivaloylmethane in diethyl ether and lithium hydroxide in aqueous solution was shown to give little or no isotopic separation. Column studies of the carbonate system exchange reaction were concluded with a 40°C run. Slightly higher enrichment of N15 was obtained than at 30°C . The temperature dependence of all in this system was measured between 15 and 45°C. The factor increases with temperature, showing a tendency toward a maximum near 45°C. Isotopic exchange appears to …

Continued work on the adsorbability of metal complexes from concentrated LiCl solutions and LiCl-HCl mixtures on a strong-base anion-exchange resin further demonstrated the much higher adsorbability of these complexes from LiCl solutions than from HCl solutions. The effect is believed to be due to the formation of less strongly adsorbed undissociated chloro-complex acids in the case of the HCl solutions.

A capital cost breakdown of the Idaho Chemical Processing Plant, a directly maintained remotely operated plant for processing spent enriched uranium fuel assemblies from reactors, is presented. The capital investment in the plant, including design, construction, training, and preoperational costs, an estimate of the direct costs incurred by the Atomic Energy Commission, and a proportional part of the costs of Central Facilities, including the value of the land and improvements theorem when acquired by the Commision, was $31,105,899. The cost of design and construction was $25,212,231, of which $3,773,357 was expanded on design and inspection.

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%.

A satisfactory ion-exchange-polarographic method was developed for the determination of either chromium(VI) or total chromium in Homogeneous Reactor fuels. Total chromium is determined as chromium (VI) , i.e., chromate, and in the same way as is chromium(VI), after chromium in the lower valence states is oxidized to chromate by potassium permanganate. Chromate is separated from all interfering metal ions in the fuel by ion exchange on a Dowex 50 resin column. The Chromate in the effluent is determined polarographically in approximately 0.75 M sodium hydroxide solution as supporting electrolyte. A well polarographic wave is obtained for the chromium (VI) chromium (III) reduction at a half-wave potential of -0.85 volt vs. the S.C.E. The relative standard deviation of the data for 2 μg of chromium (VI) per ml was 2%; for 4 μg of total chromium per ml, it was 3%. An ion-exchange-polarographic method was developed also for the determination of chromium(III). Chromium (III) is separated from all interfering ions in the fuel by ion exchange on a Dowex 1 resin column. The chromium (III) in the effluent is determined polarographically in a 1M ammonia-1M ammonium chloride supporting electrolyte. The wave obtained at a half-wave potential of -1.42 volt vs. the …

Methods for the determination of plutonium and uranium in highly radioactive scrup dissolver solutions have been developed. Plutonium was separated from the dissolver solutions by solvent-extraction and ion-exchange techniques and determined by potentiometric titration. Uranium was separated by ion exchange and determined by potentiometric titration. Solutions that were similar to the actual dissolver solutions and that contained known amounts of plutonium and uranium were analyzed by these methods. Evaluation of the data secured for the determination of plutonium and uranium by the methods given herein indicated that, within the limits of the precision of the methods, there was no bias. The precision of the data obtained for the determination of plutonium, expressed as the relative standard deviation, was better than 2% for plutonium in the concentration range of 0.27 to 0.64 mg/ml. The precision for uranium was estimated to be about 0.2% for uranium concentrations of 425 mg/ml. These methods and the data obtained by then are discussed in this report; the procedures are appended.

Two methods were developed for the determination of uranium metal in UF3 with other fluoride compounds. A simplified method of determination which has a relatively high degree of precision (coefficient of variation 2 per cent) is carried out by decomposing the hydride in an atmosphere of carbon dioxide and subsequently measuring the hydrogen over an aqueous solution of potassium hydroxide. The ignition of the hydride in an atmosphere of oxygen and volumetric measurement of the water at reduced pressures provide a more sensitive method of determination. The coefficient of variation of the latter procedure is 7 per cent. The yield of gas from the reaction of the hydride with ammonia and gaseous hydrogen chloride was found to be neither stoichiometric nor reproducible.

A direct titrimetric method for the determination of trivalent uranium in uranium trifluoride and mixtures of fused fluoride salts was developed. The method is based on the stoichiometric oxidation of trivalent uranium to the tetravalent oxidation state with an acidic solution of methylene blue. The sample containing trivalent uranium is dissolved at room temperature in an excess of standard methylene blue solution in a carbon dioxide atmosphere; the excess oxidant is variation of the method is 1.5 per cent for 5 mg quantities of trivalent uranium. The method was applied to various mixtures of fluoride salts containing both trivalent and tetravalent uranium.

A theoretical and experimental investigation of the coefficient for diffusion of ions across a magnetic field Is described. The resultant diffusion coefficient is found to vary inversely as the square of the magnetic field strength, in accord with the usual collison-diffusion theory. The magnitude of the coefficient is much larger (x700) than the coefficient predicted by the usual ambipolar diffusion theory. This discrepancy is resolved by showing that diffusion across a magnetic field is not ambipolar in character in most arc experiments. The final experimental and theoretical values are in good agreement, and it is unecessary to postulate any additional diffusion mechanisms, such as plasma oscillations.

Several plates of 98.7% Th - 1.2% U 235 (clad in aluminum) were irradiated in the MTR for an integrated flux of 2.6 x 10 21 neutrons/cm2. Although these samples represent an early development in bonding of aluminum to thorium and there are better methods at present, the bond proved to be quite strong and both clad and core were dimensionally stable under irradiation. The production of uranium 233 was as much as theory would indicate and the total amount of fissionable material material after irradiation and after decay of the protactinium 233 was greater than before irradiation. A fuel element of this nature appears to offer excellent potentialities from the standpoint of radiation stability.

Report that contains descriptions of the electronic equipment used with the multiple-crystal gamma-ray spectrometer.

The ORNL 86-in. cyclotron is being modified to provide for deflection of the proton beam. It is expected that operation will be resumed late in the spring. Nuclear physics work was limited, for the most part, to interpretation of previously collected data and to making preparations for utilizing the deflected beam. It was found that for certain isotopes the production rates could be almost doubled by operating at a slightly reduced energy and a much larger current. With the use of the ORNL 63-in. cyclotron, the absolute values of the electron capture and loss cross sections for 26-Mev nitrogen ions were obtained. The angular distribution of the cross sections for elastic scattering of nitrogen by nitrogen was measured at energies from 13 to 22 Mev. A double-focusing 90-deg magnet is being planned for use in identifying stable reaction products from nitrogen-induced reactions. The major components of the revised 44-in. test cyclotron were assembled and are being tested. Consideration is being given to the use of these components, along with a new 20,000-oersted magnet and a shielded cyclotron room, and if the tests are satisfactory the Laboratory will have available a machine which will accelerate N5+ ions to 81 Mev.

The installations of the beam deflector in the ORL 86-inch Cyclotron is sufficiently complete to allow initial testing the system permits the optional use of high-current internal targets. A survey of [illegible] cross sections made with 14-Mev neutrons indicates qualitative agreement with statistical theory. An internal-conversion ion spectrograph and a fission-fragment spectrograph were built and put in operation. The [illegible] functions severed proton-induced reactions of possible use in isotope production were measured. A capsule-type target is being used for the irradiation of chemical compounds. Nuclear physics research with 26-Mev nitrogen lens from the ORNL 63-inch Cyclotron concerned the following: a theoretical interpretation of elastic nitrogen-nitrogen scattering a detailed investigation of some nitrogen-nitrogen nuclear reactions; the measurement of reactions across sections in boron and aluminum; and the identification and the energy spectre of protons and alpha particles resulting from nitrogen-induced reactions with light elements. A study is being made of the practicality of a fixed-frequency cyclotron to accelerate protons to about 1 [illegible] for application in [illegible] research. Phase compensation would be obtained with an unusual magnetic-field configuration which has eight [illegible] cycles with about 72 deg of spiral, Also, a proposal was made to convert the 44-in. proton cyclotron a …

Bench scale studies have been made of the recovery of uranium from acid leach liquors (and slurries) by solvent extracting with di (2-ethylhexyl) phosphoric acid in an organic diluent. Uranium may be stripped from the organic solvent by either alkaline or acidic reagents, the former having been studied in greater detail. On the basis of these tests, a recovery process may be considered which shows promise both from the standpoint of operation and chemical costs. Under proper conditions, vanadium can also be extracted by the di (2-ethylhexyl) phosphoric acid and stripping again may be accomplished with either acidic or alkaline reagents. Preliminary studies have been made of these possibilities. In addition to di (2-ethylhexyl) phosphoric acid, some other organophosphorus acids, have been cursorily examined in respect to their extraction and/or stripping performance.

Two 500-kw fused-fluoride-to-Nak heat exchangers, two 500-kw NaK-to-air radiators, and a 20-tube high-velocity heat exchanger were fabricated for a heat-exchanger development program. A construction procedure, utilizing both inert-arc-welding and high temperature dry-hydrogen brazing, was used successfully on all of the units. The tube-to-header joints were welded and back-brazed; the manifold joints were inert-arc-welded with full penetration; and the tube-to-fin joints were brazed. A detailed description of the fabrication of each type of component is discussed and a cost analysis of the 500-kw units is presented.

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.

Experience in handling and purifying rubidium metal, prior to high-temperature corrosion testing, has been obtained. Some of the physical and chemical properties of this metal are listed. Distillation and filtration experiences are described, and the analysis of samples following such purification procedures are given. Stripping procedures following corrosion testing are discussed briefly. Results of preliminary corrosion experiments indicate that Inconel in a satisfactory container material for boiling rubidium at temperatures up to 1520°F.

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.