Chemistry & Biochemistry Theses and Dissertations

Permanent URI for this collectionhttp://hdl.handle.net/1903/2752

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1987 - 19892

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Start date: 1987End date: 1989

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    Experimental and Theoretical Characterization of Effective Interactions Near 132Sn
    (1987) Stone, Craig A.; Walters, William B.; Chemistry; Digital Repository at the University of Maryland; University of Maryland (College Park, MD)
    Experimental investigations have been undertaken to study the multiplet structure in six nuclei near 132Sn: 132,130Sb, 131,129,127Sb, and 132Te. Experiments were performed using ion beams of mass-separated fission products produced by the TRISTAN mass separator at Brookhaven National Laboratory. Extensive four-detector gamma-gamma coincidences, gamma-multiscaling and conversion-electron data have been collected. Ultralarge shell model calculations were performed using the VLADIMIR shell model code on the Cray/CDC 7600 supercomputer system at Lawrence Livermore National Laboratory. These calculations were designed to look at the performance of the Kallio-Kolltveit and Siemen's g-matiix potentials on the 1-3 quasiparticle nuclides in the gddsh model space. Results show that realistic potentials work well on nuclei near 132Sn but show problems with 129,130Sn and 131Sb which can not be accounted for by core-polarization corrections. Problems are shown to be due to the use of a potential derived with the Scott-Moszkowski separation metl1od. The separation distance was demonstrated to have a weak dependence on the principal quantum number but a strong dependence on the orbital angular momentum. This suggests the Kallio-Kolltveit potential is underestimating the strength of the h11/2 interactions in 129,130Sn and 131Sb.
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    The Role of Hydrogen Cyanide in Chemical Evolution
    (1989) Navarro-González, Rafael; Ponnamperuma, Cyril; Chemistry; Digital Repository at the University of Maryland; University of Maryland (College Park, Md)
    Two major research areas are investigated: The electrosynthesis of hydrogen cyanide; and the role of cyanocomplexes in the free - radical oligomerization of hydrogen cyanide. The electric discharge production of hydrogen cyanide from a simulated primitive atmosphere composed of methane, nitrogen and water vapor was investigated. The radiation chemical yield (G) of formation of HCN was determined to be 0.26. A free radical mechanism was proposed to account for the observed chemical changes. Computer simulations of the reaction mechanism could effectively model the early stages of electrolysis of the gas mixture, and permitted the estimation of the rate of electrosynthesis of hydrogen cyanide under various atmospheric conditions . The possible role of cyanocomplexes of transition elements on the free- radical oligomerization of hydrogen cyanide was investigated. Aqueous, oxygenfree, dilute solutions of hydrogen cyanide and hexacyanoferrate(II) or (III) were submitted to various doses of gamma irradiation. The presence of either cyanocomplex led to a significant decrease in the rate of decomposition of hydrogen cyanide. The major products were ammonia and carbon dioxide . Computer simulations of these systems permitted the elucidation of the reaction mechanism and the derivation of rates of reactions of free- radicals with the cyanocomplexes. The results obtained provide an insight into the possible role of cyanocomplexes of transition elements in chemical evolution.