Abstract: "A method has been established for the estimation of volatile organic acids in aqueous process solutions containing UNH, nitric acid, ANN, sodium dichromate and small amounts of hexone. The practice is to distill a 400 ul or 500 ul sample in the presence of an excess of phosphoric acid and ferrous sulfate under a high vacuum; a special apparatus utilizing a receiver cooled with a dry ice-isopropanol mixture is employed. The distillate is taken up in isopropanol and then titrated potentiometrically with standard potassium hydroxide solution. Since nitric acid and organic acids are present, two end points are observed. The potassium hydroxide added between these end points is equivalent to the organic acids. In the titration, CO2 from the atmosphere or in the potassium hydroxide is a source of error. The former was avoided and correction was made for the latter."

Reactivity measurements conducted in the Hanford Test Pile are interpreted to yield resonance integrals for uranium, uranium oxide, thorium and thorium oxide. The experiments were made using cadmium filters and are discussed in terms of the multiplication factor of the Hanford Test Pile.

Impurities are separated from plutonium solutions by means of TTA (thenoyltrifluoracetone) extractions. Plutonium in hydrochloric acid solution is reduced to the trivalent state with hydroxylamine, and some impurities are extracted into hezone or a solution of TTA in hezone. The organic phase is removed, and the plutonium in the aqueous phase is oxidized to the tetravalent state with nitric acid. Investigations of several variables which affect the extraction are described..