Technical report that information has bee obtained on the effect of beta and gamma radiation on the electrical resistance of insulating materials The results are summarized. The recovery to original resistance values has been measured. In general, the initial rate is rapid for the first few hours; the rate then decreases sharply. Certain samples show evidence of complete recovery. Effects on mechanical properties of several plastics has also been studied. Data on gas evolution from several organic materials including those suggested by the physiological shield have been extended to include both beta and deuteron bombardments. Samples of "Press-wood" are being evaluated. The effect of current on the H2O2 production in water containing I- has been studied at several I- concentrations. Water contain-dissolved CO2 shows the presence of oxidant (presumably H2O2). H2O2 has been produced by recoil protons from the scattering of fast neutrons in de-oxygenated water. Radioactive solutions do not greatly affect the applicability the glass electrode providing the electrode is thoroughly washed with distilled water before immersion in the standard buffer solution.

Abstract: Experiments on colloid milling and pumping show that uranium trioxide, when carefully dehydrated, can be dispersed in water to form a relatively stable slurry, suitable for a homogeneous slurry pile. At temperatures considerably below those of anticipated pile operation particle size growth occurs attended by increase in settling rate and decrease in viscosity. Theses properties of the slurries may be strongly affected by impurities present as well as by special operating conditions.

Abstract. the electrodeposition of uranium metal, in the form of tree-like deposits, from molten strontium halide baths is described. Under the best conditions studied, approximately 40% recovery is attained. Freedom from side-reactions of the reduced uranium with anode products and/or refractory materials, and high cathode current densities appear to be essential to the success of the process. the refining of uranium under similar conditions appears to occur quite readily, with approximately 50% current efficiency. The preparation of UI3 is also described.

Technical report with short reports on (1) Effect of radiation on water and aqueous systems; (2) Gas evolution from uranyl solutions; (3) Effect of radiation on solid compounds; (4) Instruments; and (5) Scattering.

Introduction. Some forty different uranium compounds have now been given diffraction study at Ames. Reports of these investigations are scattered in the Project literature; many have been reported in a sentence or two as a note along with chemical or metallographic reports. To make the results of this crystal structure work more available this summary of the Ames work has been compiled. (A similar summary has already been published from the Chicago laboratory.)

Technical report discussing that the deuterium concentration of heavy water can be determined by equilibrating the water with deuterium gas in the presence of a catalyst with subsequent analysis of the equilibrated gas on the mas spectrometer. The apparatus for equilibration analyses maybe be considered in three parts: 1) apparatus for introducing the ingredients into the reaction chambers; 2) the reaction chambers; 3) the mass spectrometer for analysis of the equilibrated gas. The isotopic composition of the deuterium gas to be used as the starting material is primarily governed by what gases are available. In general it is best to use gas within about one percent on either side of the final equilibrium composition. No reaction takes place between deuterium gas and water molecules in the absence of a catalyst. Platinum oxide is used as the catalyst.

Abstract. The distribution coefficient of U(VI) between perchloric acid solutions and benzene solutions of TTA has been measured as a function of the acidity. It was possible to interpret the data in terms of the charge on the U(VI) species present in the aqueous phase. The experiments indicate that U(VI) exists as an ion charge +2 at acidities from 0.1M to 2.5M. In the interpretations of the distribution data, it was necessary to know the acidity coefficient of the uranyl chelate in the benzene solution. This was determined by measurement of the solubility of the compound UO2K2 - xH2). The activity coefficient of UO2K2 was found to decrease rapidly as the concentration of TTA in the benzene phase increased above 0.1M. This is probably due to the formation of a species involving more than two TTA molecules per U(VI)