Abstract. The separation of uranyl nitrate from aqueous solutions of 0.635 M thorium nitrate, 3 M nitric acid and 3 M calcium nitrate by extraction with organic solvents has been investigated. Solvents which gave good separations were 2-tthyl hexyl acetate, ethyl benzoate, n-butyl either and beta-beta- dichloroethyl ether. In general, higher esters, ethers and alcohols are better for separating uranium from thorium that the lower homologues. Several solvents were tested at lower nitric acid concentrations. Dibutyl cellosolve gave a very good separation when the solution was 0.1 M nitric acid. Of the solvent mixtures studied that of equal parts of n-butyl ether and dibutyl cellosolve gave a good separation.

Abstract. The physico-chemical methods of determining nitric acid and thorium nitrate in solutions containing these two materials were investigated. Conductimetric titration with sodium hydroxide can be used to determine nitric acid accurately. the titration of thorium nitrate requires a separate standardization of the base however, since a basic salt is precipitated rather the normal hydroxide. The titration of thorium is reproductible however, so and empirical standardization can be used. The measurement of the specific gravity and refractivity of the solutions provides a method of determining the concentrations in terms of these two variable. Equations for the concentrations in terms of specific gravity and refractively are given, both in pure solutions and in those saturated with methyl isobutyl ketone.

Report discussing studies regarding porphyrin excretion and hemoglobin metabolism in animals with phenylhydrazine anemia, and studies regarding the coproporphyrin and protoporphyrin in the red blood cells of rabbits.

Technical report regarding he purpose of the investigation was to evaluate the Chicago mass spectrograph as an analytical instrument for solids.

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.

A supplementary report on Inter River District Green River Desert Area, Utah, regarding a careful estimation of the potential pore reserves of the area.