Browsing by Subject "nuclear waste"
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Item Development of Pillared M(IV) Phosphate Phosphonate Inorganic Organic Hybrid Ion Exchange Materials for Applications in Separations found in the Nuclear Fuel Cycle(2012-10-02) Burns, JonathanThis dissertation focuses on key intergroup and intragroup separations found in the back end of the nuclear fuel cycle, specifically americium from lanthanides and americium from other actinides, most importantly americium from curium. Our goal is to implement a liquid-solid separation process to reduce waste and risk of contamination by the development of metal(IV) phosphate phosphonate inorganic organic hybrid ion exchange materials with the ideal formula of M(O6P2C6H4)0.5(O3POA) * nH2O, where M = Zr or Sn, A = H or Na. These materials have previously shown to have high affinity for Ln, this work will expand on the previous studies and provide methods for the above target separation, exploiting oxidation state and ion charge to drive the separation process. The optimum hydrothermal reaction conditions were determined by adjusting parameters such as reaction temperature and time, as well as the phosphonate to phosphate (pillarto-spacer) ligands ratio. Following these results four bulk syntheses were performed and their ion exchange properties were thoroughly examined. Techniques such as inductively coupled mass spectrometry and liquid scintillation counting were used to determine the affinity of the materials towards Na+, Cs+, Ca2+, Sr2+, Ni2+, Nd3+, Sm3+, Ho3+, Yb3+, NpO2+, Pu4+, PuO22+, Am3+, AmO2+, and Cm3+. Separation factors in the thousands have been observed for intergroup separations of the Ln from the alkali, alkaline earth, and low valent transition metals. A new method for Am oxidation was developed, which employed Na2S2O8 as the oxidizing agent and Ca(OCl)2 as the stabilizing agent for AmO2+ synthesis. Separation factors of 30-60 for Nd3+ and Eu3+ from AmO2+, as well as 20 for Cm3+ from AmO2+ were observed at pH 2. The work herein shows that a liquid-solid separation can be carried out for these difficult separations by means of oxidation and ion exchange.Item Evaluation of zirconium-iron-rhenium alloys as surrogates for a technetium alloy waste form(2009-05-15) Mews, Paul AaronStainless steel ? zirconium alloys were developed by the US Department of Energy Laboratories as metallic waste forms for noble metal fission products. This thesis evaluates iron?zirconium?rhenium alloys to establish a technical basis for using metal waste form alloys for technetium-99 immobilization. Rhenium is used as a surrogate for Tc-99 since Tc is not naturally available and Re is metallurgically similar to Tc. The iron-zirconium system has two eutectic compositions, Fe-15 wt % Zr and Zr- 16 wt% Fe. Ten test samples were successfully cast in yttrium oxide crucibles at 1600?C, half near each eutectic composition, with Re amounts varying from 2.5 to 12.5 weight percent. A scanning electron microscope (SEM) with energy dispersive X-ray spectroscopy (EDS) capability was employed to determine the phase structure and phase composition of each sample. Iron rich samples were found to form up to three phases, with the rhenium content favoring the intermetallic phases: 1) an Fe solid solution phase, 2) an FeZr2-type intermetallic with 11 wt % or less Re, and 3) a second intermetallic with about 18 wt % Re. Zirconium rich samples formed as many as five distinct phases: 1) a Zr solid solution phase, 2) a Zr3Fe-type intermetallic with as much as 13 wt% Re, 3) a rhenium-zirconium intermetallic, 4) another Fe-Zr intermetallic with very little Re, and 5) a Fe-Re intermetallic. Potentiostatic and potentiodynamic electrochemical tests were performed using sulfuric acid to evaluate the corrosion resistance of each sample. These tests found that the zirconium rich samples were very corrosion resistant but became increasingly susceptible at higher rhenium concentrations. The iron rich samples were not very resistant to corrosion under the test conditions; there was no notable trend in corrosion behavior related to the introduction of rhenium.