Physical Sciences and Mathematics Commons^™

Enrichment Of Tin Activity Through The Szilard-Chalmers Separation, Herta W. Spano

Chemistry and Chemical Biology ETDs

It was the purpose of this investigation to utilize the Szilard-Chalmers reaction in order to prepare tin solutions of high specific activity.

Tetraphenyl tin was chosen for the target compound. It is a white, crystalline solid of excellent thermal stability. No data have been reported in the literature on the rate of exchange between inorganic forms of tin and tetraphenyl tin but it seemed highly probable that this exchange would be very slow. Tetraphenyl tin is soluble in various organic solvents but insoluble in water, and this suggested solvent extraction as a possible means of separation of the activated tin …

Derivatives Of M-Xylene, Henry J. Muller

Chemistry and Chemical Biology ETDs

Since m-xylene of 95-98% purity has recently become available from petroleum, this is an appropriate time to prepare an examine its derivatives. Isophtalic and m-toluic acids can be prepared from the hydrocarbon. The purpose of this work was to prepare imidazolines from these acids

The Chemical Characteristics Of 8.0-Day I^131 Produced By The Beta Decay Of 25-Minute Te^131 In Organic Liquids, Francis J. Keneshea Jr.

Chemistry and Chemical Biology ETDs

In 1934 Szilard and Chalmers found that a large fraction of the radioactive iodine produced in the thermal neutron irradiation of ethyl iodide could be extracted from the irradiated material. The procedure followed was to add a trace of carrier iodine to the irradiated liquid, extract the iodine with an aqueous solution of a reducing agent and precipitate the iodide as silver iodide. The silver iodide precipitate obtained in this manner contained a large fraction of the iodine activity (25-minute I¹²⁸), at a high specific activity. Since ethyl iodide is not soluble in water and hence is not …

The Kinetics Of The Exchange Between Benzyl Iodide And Iodide Ion, Paul Stillson

Chemistry and Chemical Biology ETDs

In the investigation to be described here, the exchange reaction was carried out in methyl alcohol, ethyl alcohol, and acetone-alcohol mixtures. Radioactive I¹³¹ was used as a tracer throughout the investigation. A mechanism was postulated for this reaction in each solvent and activation energies were determined.