Abstract. The effect of various inhibitors on the production of CrIII in W waters containing chromatic has been studies at a variety of pH's in the CP-3 pile. The addition of 2 ppm NaClO3 appears to have little effect a a pH of 5.3, but 2 ppm NaClO3 cr 0.15 ppm of Cl2 (in the form of NaOCl) somewhat decreases the amount of chromatic reduced at a pH of 7.1. The inhibition is not great enough, however, to reduce the amount of CrIII formed to the maximum concentration permissible at W (0.02 ppm). The addition of 3 ppm (NH4)2S2O3 as an inhibiter will permit W water to be used a a Ph of 7.0, but not at a pH of 6.5 as far as chromate reduction is concerned. The concentration of CrIII would be 0.01 ppm and 0.05 ppm, respectively, after one passage through the pile. Previous conclusion as to the effects of temperature, pH, intensity and the addition of ammonium persulfate, which had been reached from experiments with simulation W water, have been checked by studies with solutions made from water chipped directly from Hanford. All of the effects noted were found to be similar to those already reported, …

Abstract. In addition to the hexagonal and monoclinic bismuth phosphate precipitates, whose structures are now known, a third crystalline phase has been found to appear in BiPO4 precipitates after (a) extremely long digestion in concentrated nitric acid; (b) oven drying at 800 degrees to 1000 degrees. Thought very small single crystals of the component have been isolated, nor crushed sample contained less than 30% of the beta-form. The cell size and symmetry of the crystal indicates that there ae two bismuth atoms in the cell, and there is no evidence that the compound is not BiPO4. It is suggested that this maty be a third form of BiPO4, stable over a short range of conditions, and tending to revert to the beta-form.

Abstract. to estimate the oxygen picked up by thorium in casting a rapid method of running the acid insoluble content was developed. the quickest procedure consists of reacting with mixed acids, fuming with perchloric and filtration to separate the "free" thorium from the "combined". The precipitate is ignited and weighed as thorium dioxide.

.Technical report describing the transference experiments. The carrying of zirconium and columbium by ferric hydroxide has a very marked dependence on pH. In the experiments it was noticed that the concentration of Zr activity in various solutions changed with time This indicated that the Zr was being adsorbed on the glass. The carrier free trace is adsorbed on glass. This effect must be considered in experiments with Zr tracer in glass apparatus.

Abstract. A summary of the effect of metal, carbon, silicon, and oxygen impurities upon the various sulfide refractories is given and the proper procedures for elimination of the impurities are discussed. CeS which is properly prepared can be handled in air without danger of catching fire or appreciable oxidation. 650 satisfactory crucibles have been made to date using sulfides which were screened and pressed in air with less than 0.5% oxygen pickup. The other cerium and thorium sulfides are even more inert to oxidation than is CeS. Phase diagram possibilities are discussed for the cerium and thorium sulfide and oxy-sulfide systems. Further study of the ThS has shown that ThS crucibles are the highest melting and least volatile of the sulfide crucibles and ThS may be used for remelting of some metals up to 2000 degrees C. ThS crucibles appear to be the most suitable containers for metal reductions.

Abstract. Fluorides and other halides are hydrolyzed completely by passing a rapid stream of superheated steam over the sample near 1000 degrees C in a specially designed platinum reaction tube. The steam and hydrogen halide are condensed by cooling, and the resulting distillate titrated with standard sodium hydroxide solution. The fluorides and chlorides of the light metals, hitherto thought of as very difficult to hydrolyze, are mixed with U3O8, or other metallic oxides, which reacts with the products of hydrolysis, thus shifting the equilibrium so that the reaction is complete in a comparatively short time. A description of the apparatus, including photographs, the recommended method of procedure, hydrolysis rate graphs, and suggestions for further applications of the method are given.

Abstract. It has been established that heating samples of graphite during exposure in a pile decreases substantially the observed changes in the elastic modulus and electrical resistance caused by the irradiation. The functional relationship between the percentage changes observed and the temperature of exposure resembles the relationship between the final percentage changes and the temperature of heat treatment after exposure (cf. report CC-1668). Anomalous results reported previously for higher temperatures in CC01669 are now shown to be attributable to a destructive influence on the graphite, probably oxidation of samples exposed in air.

Abstract. In order to anticipate radiation - chemical effects in solutions of active lanthanum, various solutions and suspensions containing lanthanum were irradiated with an electron beam. Separation of lanthanum from barium by the alcoholic HCl method is not rendered less efficient by radiation, although considerable gas evolution occurs. Suspensions of lanthanum as hydroxide and as ferrocyanide are not appreciably solubilized by radiation. Lanthanum oxalate is decomposed by radiation, is partially thrown into solution, and finally dissolves completely when all the excess oxalate ion in the solution has been destroyed.

Abstract. Methods for determination of both uranium and nickel in solutions of these metals are described. Alloys can be dissolved in nitric acid treated with citric acid to complex the uranium, and the nickel precipitated as nicked dimethylglyoxime. The uranium is reduced and titrated with standard ceric sulfate. These methods are for the determination of macro amounts of uranium and nickel with errors on the order of 0.1%.

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.)

Introduction. the conventional procedures of analysis for uranium and manganese can be employed in the analysis of alloys of these metals. The alloys are reacted with perchloric acid and hydrogen peroxide, fumed to remove any chloride ions, diluted to volume and aliquots analyzed by redoximetry.

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.

This technical report summarizes the work done in attempting to determine the solubility of helium in tuballoy. In general, the method used has been to allow the tuballoy to stand in contact with helium at one atmosphere presume at a fixed temperature for an extended period, then to pump off the excess helium to a low pressure in as short a time as possible (10-6 mm of Hg or less). The system was then closed off and the pressure increase was measured by a suitable gauge as a function of time. The metal was employed in the form of a powder in early measurements, and later as massive metal. The experimental techniques are described in the report.

The work described in this technical report was undertaken as part of a larger program dealing with a systematic investigation of changes in the physical prosperities of artificial graphite due to neutron bombardment. Very pronounced among those changes is the increase in the elastic modulus. Since there is a general relationship between the elastic modulus of a given substance and its specific heat, it was expected that corresponding changes will occur in the specific heat. In conclusion, the experiments determined that it appears that the low temperature specific heat measurements of strongly bombarded samples will be helpful for the understanding of the nature and the mechanism of the changes produced by neutron bombardment and annealing.

Abstract. Methods of analysis for thorium, calcium, and nitric acid in solutions from thorium extraction purification columns are described and the results and errors are outlined. A brief description of methods of analysis that were not successful is included.

Technical report describing that the use of controlled amounts of carbonate, acting both as complexing agent buffer led to a fairly satisfactory procedure for the determination of Th in Th-U alloys, using cupferron. The alloy, dissolved in NHO2, in the presence of HF, is treated with H2SO4 and the mixture is evaporated in SO2 fumes. The solution is diluted and (NH4)2CO2 is added. Th is precipitated from this solution with cupferron. The precipitate is weighed as ThO2 after ignition. An accuracy of 6% was obtained. A method was developed specifically for the determination of Th in U-Th alloys containing 1 to 10% Th. An ion exchange resin in column is used to separate Th from U, with NH2OH-HCl as complexing agent. The Th is then precipitated, ignited, and weighed in the conventional manner.

Technical report on the studies that have been made on the composition and thermal decomposition of uranyl peroxide. The conditions of precipitation and drying have been found to have no appreciable effect on the composition of the compound, but do affect the physical appearance of the precipitate and the rate of thermal decomposition. The UO4 + 2H2O appears to be thermodynamically unstable with respect to UO3 at 25 degrees C and atmospheric pressure, although the rate of conversion is extremely slow. The UO4 + 2H2O is completely converted to UO3 on standing at 150 degrees C and atmospheric pressure for two weeks. Partially decomposed uranyl peroxide samples contain extra oxygen which is released on immersing the sample in water.

Abstract. A method for the preparation of beryllium oxide of high purity is presented. Beryllium basic acetate (BeO-3Be(C2H3O2)2) is prepared from the metal or a convenient salt, a chloroform solution of this material extracted with redistilled water, the dried basic acetate distilled in a quartz apparatus, and this purified material converted to the oxide by fuming down with sulfuric acid and igniting at 1000 degrees C. Impurities detectable spectrographically were reduced to a very low level.

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)

Technical report describing the attempt to separate the long lived fission product oxides by volatilization methods. A fractionization crucible was used. The fractionations give a fair idea of the relative volatilities of the longer lived fission products and also of the degrees of separation of the plutonium oxide or oxides from the fission products.

Abstract. Samples of pile graphite, irradiated in a test-hole at Hanford for 15 months, have been assayed for radioactive C14, yielding 0.38 ± 0.04 microcuries per gram. At this level of activity, the pile graphite contains very valuable amounts of C14. The relation between the above assay and the probable average assay of pile graphite is discussed, and it is concluded that the latter is almost certainly above 0.3 uc/ gram. Controlled oxidation of this graphite, either with oxygen at ~ 750°C, or with chromic acid "cleaning solution" at room temperature, yields early fractions which are highly enriched in C14. Concentrations of 5-fold with oxygen, and 50-fold with CRO{sub3}, have been observed. The relation between the observed enrichment and the Wigner effect is discussed, and a mechanism accounting for the observations put forward. According to this, about 25% of the stable carbon atoms in the lattice have been displaced by Wigner effect, a large fraction of which have healed the migrating to crystal edges. All the C14 atoms have been displaced, and the same fraction of these migrate to the edges. The enrichment then results from surface oxidation, in the oxygen case. Predictions are made on the basis of this …

Technical report with short reports on (1) P-9 recovery from UO2F2 solution; (2) Correlation of theories on action of radiation on matter; (3) Literature surveys on organic compounds and on chemistry of UO2F2; (4) effect of radiation on organic compounds; and (5) Effect of radiation on 100 area construction materials.

Technical report: The apparatus for the low pressure combustion method of determining carbon in iron and steel has be redesigned to increase the speed of manipulation. It has been tested by running several thousand determinations and found to yield results in good agreement with Wooten's form of the apparatus. A detailed description of the equipment and its manipulation is given together with an account of experimental studies on the method. Results are also shown for the carbon content of copper.

Technical report with short reports on (1) Heavy water analysis and standardization, and Specific gravity of pure D2O; (2) Homogenous exponential experiment; (3) Recombination of pile gases; (4) Slurry pumping studies; and (5) Electron microscope laboratory.