Made available in DSpace on 2014-10-09T12:33:09Z (GMT). No. of bitstreams: 0 / Made available in DSpace on 2014-10-09T14:06:16Z (GMT). No. of bitstreams: 0 / A obtenção de urânio metálico é fundamental para produção de elementos combustíveis que alimentam reatores nucleares de pesquisa e que fabricam radioisótopos e radiofármacos. No IPEN, o urânio metálico é obtido via redução magnesiotérmica do UF4. Essa reação é realizada em um cadinho fechado de grafite inserido em um reator metálico vedado e evitando contato com o meio exterior. O conjunto é aquecido gradualmente em um forno poço, até que se atinja a temperatura de ignição da reação (entre 600-650oC). A modelagem do perfil de aquecimento do sistema pode ser realizada empregando programas de simulação pelo Método dos Elementos Finitos. Através dos perfis térmicos no corpo da carga, têm-se uma noção do período de aquecimento necessário para que a reação ocorra, possibilitando a identificação da mesma em um agrupamento de maior ou menor rendimento em urânio metálico. Estima-se as propriedades térmicas do UF4, determinando sua condutividade térmica e capacidade térmica empregando o Método Flash Laser, bem como as propriedades térmicas da carga UF4 + Mg. Os resultados obtidos são comparados a testes laboratoriais realizados para a simulação preliminar do processo de produção. / Dissertacao (Mestrado) / IPEN/D / Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP

<p> The addition compounds of selenium tetrafluoride with sulfur trioxide, boron trifluoride, and arsenic, antimony, bismuth, vanadium, niobium and tantalum pentafluorides have been prepared. These compounds have been studied in the solid state using X-ray powder diffraction, and infra-red and Raman spectroscopy; in the molten state using Raman spectroscopy, nuclear magnetic resonance spectroscopy, and conductimetric and viscosity measurements; and in solution using Raman spectroscopy, cryoscopy, conductivity and nuclear magnetic resonance spectroscopy.</p> <p> The compound SeF4SO3 has a fluorosulfate-bridged polymeric structure. The remaining compounds have fluorine-bridged structures, this interaction being the strongest in SeF4BF3 and SeF4VF5 and decreasing in the order SeF4NbF5 SeF4TaF5 SeF4AsF5 SeF4SbF5 SeF4BiF5.</p> <p> The characteristics of the SeF3+ group are discussed. The properties of fluorine bridging and various methods of detecting such interactions are also considered.</p> / Thesis / Doctor of Philosophy (PhD)

京都大学 / 新制・課程博士 / 博士(エネルギー科学) / 甲第23295号 / エネ博第420号 / 新制||エネ||80(附属図書館) / 京都大学大学院エネルギー科学研究科エネルギー基礎科学専攻 / (主査)教授 萩原 理加, 教授 野平 俊之, 教授 坂口 浩司 / 学位規則第4条第1項該当 / Doctor of Energy Science / Kyoto University / DFAM

This thesis project aims to develop an innovative technique for the production of high-purity uranium nitride (UN) through the ammonolysis of fluorides. The desired objective is to perform a controlled gas/gas reaction between uranium hexafluoride (UF6) and ammonia (NH3) at 800°C. The intermediate product thereby obtained (uranium dinitride, UN2) is subjected to further heating up to 1100°C under argon atmosphere, to ultimately produce UN. An inherent challenge faced in previous experiments was related to the dissociation of ammonia, which is alimiting factor for upscaling. Therefore, in this project a new setup is invented to address this challenge and it is proved experimentally: the idea is to achieve a coaxial laminar flow of UF6 and a carrier gas, where a central stream of the former is shielded by the latter so that the tworeacting gasses mix only in the hot point of the furnace, where the desired reaction can happen. To implement this approach, the ammonia dissociation has been studied, an apparatus for the controlled evaporation of UF6 has been designed and built, and two different injection nozzleshave been tested in different setup configurations. Eventually, the complete prototype has been tested altogether in a synthesis experiment at 800°C, and the products thus obtained have been converted into UN at 1100°C. Numerous auxiliary experiments have been performed using UF4as a reactant, as it is easier to handle and the results thus obtained can be largely extended to UF6. Lastly, a UF4 synthesis experiment has been performed, as educationally helpful to further dig into some chemistry features of this material, and a UN pellet has been sintered with Spark Plasma Sintering (SPS). / Detta examensarbete syftar till att utveckla en innovativ teknik för framställning av urannitrid (UN) med hög renhet genom ammonolys av fluorider. Målsättningen med arbetet är att utföra en kontrollerad gas/gasreaktion mellan uranhexafluorid (UF6) och ammoniak (NH3) vid 800°C. Den därigenom erhållna mellanprodukten (urandinitrid, UN2) värms därefter upp till 1100°C i en argonatmosfär, för att slutligen producera UN. En utmaning i tidigare experiment var relaterat till dissociationen av ammoniak, vilket är en begränsande faktor för uppskalning av processen. För att möta denna utmaning utvecklas därför en ny process i detta projekt och den bevisas experimentellt. Tanken är att skapa ett koaxiellt laminärt flöde bestående av UF6 och en bärgas, där en central ström av den första är avskärmad av det senare så att de två reagerande gaserna enbart blandas i ugnens heta zon, där den önskade reaktionen sker. För att implementera denna metod så har ammoniakdissociationen studerats, en apparat för kontrollerad avdunstning av UF6 har designats och byggts, och två olika insprutningsmunstycken har testats i olika konfigurationer. Den kompletta prototypen har testats i sin helhet med ett syntesexperiment vid 800°C, och produkterna som erhållits har konverterats till UN vid 1100°C. Ett flertal hjälpexperiment har utförts med UF4 som reaktant, eftersom den är enklare att hantera, och de erhållna resultaten kan till stor del utvidgas till UF6. Slutligen har ett UF4-syntesexperiment genomförts för att som ett pedagogiskt hjälpmedel ytterligare studera vissa kemiska egenskaper hos detta material. En UN-pellet har sintrats med starkströmsassisterad varmpressning (eng. Spark Plasma Sintering, SPS).

Zirconium tetrachloride (ZrF4) is extensively used in the manufacturing of zirconium metal. The concept of producing zirconium tetrafluoride from dissociated zircon and ammonium bifluoride is well established at the South African Nuclear Energy Corporation (Necsa) State Owned Company (SOC) Limited. Zirconium and hafnium are always found in the same minerals. In nuclear application zirconium is used for structural construction and as a cladding material for fuel, because of the low thermal neutron absorption, while hafnium is used as control rod in nuclear reactor, because of the high thermal neutron absorption. The methods of separating hafnium from zirconium prefer the use of ZrCl4 than ZrF4. This is because of the high solubility in both aqueous solutions and organic solvents and low sublimation temperature of ZrCl4, while ZrF4 is almost insoluble in organic solvent and has a high sublimation temperature. Thermodynamic evaluations showed that chlorinating ZrF4 with either CaCl2, KCl, LiCl or NaCl respectively was not favourable, while chlorinating ZrF4 with either BeCl2 or MgCl2 was favourable. But due to cost consideration chlorinating ZrF4 with BeCl2 was not investigated. A thermogravimetric apparatus was used to investigate the isothermal and the non-isothermal kinetics of chlorinating analytical grade ZrF4 with MgCl2. The thermogravimetric apparatus revealed that chlorination of ZrF4 commence at temperature above 350°C. Isothermal kinetics of chlorinating analytical grade ZrF4 with MgCl2 was investigated at temperatures of 400, 450, 480, 500°C. The reaction progressed towards completion prematurely before the isothermal temperatures were reached, due to a low heating rate of 20 °C/minutes was used to heat up the reaction mixture to the desired isothermal temperatures. As a result, the isothermal kinetics could not be determined. Heating rates of 5, 10, 15 and 20 °C/minutes were used to investigate the non-isothermal kinetics. The apparent activation energy of chlorinating ZrF4 with MgCl2 varied significantly when the non-isothermal kinetics was investigated. The variation was due to changes in the reaction mechanism. As a result, rate law of chlorinating ZrF4 with MgCl2 could not be determined due to variation of the apparent activation energy. Crude ZrF4 prepared at Necsa SOC ltd. was chlorinated with MgCl2, a mixture of MgCl2 and KCl, a mixture of MgCl2 and LiCl, and a mixture of MgCl2 and NaCl respectively. Chlorination of the crude ZrF4 was conducted at temperatures of 400, 450 and 500°C respectively. The aim of chlorinating the crude ZrF4 was to investigating the effect of the chlorinating on the purity of the produced ZrCl4. A batch reactor was used in this study. The reactor was divided into two sections, namely the reaction zone and the condensation zone. The diameter of the condensation zone was larger than that of the reaction zone. Reactants were placed into the reaction zone and the products were collected at the reaction zone and the condensation zone. Samples were collected from these products and analysed using for X-Ray Diffraction analysis (XRD) and Inductive Coupled Plasma Optical Emissions Spectroscopy (ICP-OES). XRD was used to identify the compounds that were present in the products and ICP-OES was used to determine the concentration of the elements that were present in the products. The analysis of the results obtained showed that the highest recovery of zirconium in the products collected from the condensation zone, the sublimed products, was achieved by chlorinating ZrF4 with MgCl2 at 500°C. About 80% was recovered. About 96% of the concentration of the impurities in the sublimed products was reduced when ZrF4 was chlorinated with a mixture of MgCl2 and LiCl at 450°C. About 36% of hafnium in the sublimed products was reduced when ZrF4 was chlorinated with a mixture of MgCl2 and NaCl at 400°C. / Chemical Engineering / M.Tech. (Chemical Engineering)

Zirconium tetrachloride (ZrF4) is extensively used in the manufacturing of zirconium metal. The concept of producing zirconium tetrafluoride from dissociated zircon and ammonium bifluoride is well established at the South African Nuclear Energy Corporation (Necsa) State Owned Company (SOC) Limited. Zirconium and hafnium are always found in the same minerals. In nuclear application zirconium is used for structural construction and as a cladding material for fuel, because of the low thermal neutron absorption, while hafnium is used as control rod in nuclear reactor, because of the high thermal neutron absorption. The methods of separating hafnium from zirconium prefer the use of ZrCl4 than ZrF4. This is because of the high solubility in both aqueous solutions and organic solvents and low sublimation temperature of ZrCl4, while ZrF4 is almost insoluble in organic solvent and has a high sublimation temperature. Thermodynamic evaluations showed that chlorinating ZrF4 with either CaCl2, KCl, LiCl or NaCl respectively was not favourable, while chlorinating ZrF4 with either BeCl2 or MgCl2 was favourable. But due to cost consideration chlorinating ZrF4 with BeCl2 was not investigated. A thermogravimetric apparatus was used to investigate the isothermal and the non-isothermal kinetics of chlorinating analytical grade ZrF4 with MgCl2. The thermogravimetric apparatus revealed that chlorination of ZrF4 commence at temperature above 350°C. Isothermal kinetics of chlorinating analytical grade ZrF4 with MgCl2 was investigated at temperatures of 400, 450, 480, 500°C. The reaction progressed towards completion prematurely before the isothermal temperatures were reached, due to a low heating rate of 20 °C/minutes was used to heat up the reaction mixture to the desired isothermal temperatures. As a result, the isothermal kinetics could not be determined. Heating rates of 5, 10, 15 and 20 °C/minutes were used to investigate the non-isothermal kinetics. The apparent activation energy of chlorinating ZrF4 with MgCl2 varied significantly when the non-isothermal kinetics was investigated. The variation was due to changes in the reaction mechanism. As a result, rate law of chlorinating ZrF4 with MgCl2 could not be determined due to variation of the apparent activation energy. Crude ZrF4 prepared at Necsa SOC ltd. was chlorinated with MgCl2, a mixture of MgCl2 and KCl, a mixture of MgCl2 and LiCl, and a mixture of MgCl2 and NaCl respectively. Chlorination of the crude ZrF4 was conducted at temperatures of 400, 450 and 500°C respectively. The aim of chlorinating the crude ZrF4 was to investigating the effect of the chlorinating on the purity of the produced ZrCl4. A batch reactor was used in this study. The reactor was divided into two sections, namely the reaction zone and the condensation zone. The diameter of the condensation zone was larger than that of the reaction zone. Reactants were placed into the reaction zone and the products were collected at the reaction zone and the condensation zone. Samples were collected from these products and analysed using for X-Ray Diffraction analysis (XRD) and Inductive Coupled Plasma Optical Emissions Spectroscopy (ICP-OES). XRD was used to identify the compounds that were present in the products and ICP-OES was used to determine the concentration of the elements that were present in the products. The analysis of the results obtained showed that the highest recovery of zirconium in the products collected from the condensation zone, the sublimed products, was achieved by chlorinating ZrF4 with MgCl2 at 500°C. About 80% was recovered. About 96% of the concentration of the impurities in the sublimed products was reduced when ZrF4 was chlorinated with a mixture of MgCl2 and LiCl at 450°C. About 36% of hafnium in the sublimed products was reduced when ZrF4 was chlorinated with a mixture of MgCl2 and NaCl at 400°C. / Chemical Engineering / M.Tech. (Chemical Engineering)

Ziel dieser Doktorarbeit war es, den Einfluss von verschiedenen Parametern auf die spektroskopischen Eigenschaften von Lanthanid-basierten Aufkonversions-Materialien zu erforschen. Ein besonderer Fokus lag dabei auf hexagonalen Natrium-Yttrium-Tetrafluorid Kristallen, die mit dreifachgeladenen Yb und Er oder Tm Ionen kodotiert wurden. Eine wesentliche Voraussetzung für mögliche Anwendungen dieser Kristalle ist ein Verständnis aller ihrer wichtigen photophysikalischen Besonderheiten. Die erste Studie dieser Doktorarbeit untersuchte daher, wieso Nanokristalle viel weniger absorbierte in ausgesendete Photonen umwandeln als mikrokristalline Teilchen. Die Ergebnisse zeigten, dass man ungeschalte Kristalle aufgrund von Oberflächen-Lösch-Effekten in zwei Teile unterteilen kann, einen strahlenden Kern und eine Schale aus stark oder vollständig gelöschten oberflächennahen Lanthanid-Ionen, welche für Kristalle abnehmender Größe einen immer größeren Volumenanteil einnimmt. Die zweite Studie untersuchte exemplarisch, ob eine kompliziertere Partikelarchitektur, bestehend aus einem einfach-dotierten Er Kern und Yb als Schalenmaterial, diesen Effizienzverlust der Lumineszenz reduzieren kann. Die Ergebnisse zeigten jedoch, dass dies nicht der Fall ist. Eine weitere Studie untersuchte den Einfluss der Konzentration der Tm Ionen in Yb, Tm kodotierten Nanokristallen auf die spektroskopischen Eigenschaften dieser Materialien und zeigte, dass für eine maximale Emission im Lichtwellenbereich über 700 nm andere Tm Konzentrationen benötigt werden als für maximale Lichtemissionen in den unteren Lichtwellenbereichen. Die letzte Studie untersuchte den Einfluss eines zuvor berichteten Zersetzungsprozesses von exemplarisch ausgewählten Yb, Tm kodotierte Nanokristallen in wässrigen Dispersionen auf deren spektroskopische Eigenschaften. Mithilfe dieser Ergebnisse war es möglich, mehrere Emissionsbanden als Parameter für das Langzeit-Stabilitäts-Monitoring dieser Materialien zu identifizieren. / This PhD thesis investigated the influence of various parameters on the spectroscopic properties of so-called upconversion nanoparticles (UCNPs). A special emphasis was dedicated to hexagonal-phase sodium yttrium tetrafluoride crystals that were codoped with trivalent Yb and either Er or Tm ions. Such UCNPs can, however, experience no breakthrough in the field of UC nanotechnology before all of their important photophysical features are understood. The first study of this PhD thesis therefore investigated, why nanocrystalline upconverters with different surface chemistries convert less absorbed to emitted photons than their microcrystalline counterparts. The results revealed that upconverting crystals apparently have to be subdivided into two parts, with one being the luminescent core and the other being a completely dark shell that is quenched by surface effects and assumes an ever increasing volumetric content for small UCNPs. The second study exemplarily investigated, if a more complex particle nanostructure that consisted of a Er doped core, surrounded by a Yb doped shell, could overcome these efficiency losses, however, it concluded that it does not. Another study explored the influence of Tm doping concentrations of Yb, Tm codoped nanocrystals on their spectroscopic properties and concluded that different Tm doping concentrations are required for a maximum upconversion luminescence in the wavelength regions above 700 nm, than for the wavelength regions below that. The last study of this PhD thesis investigated the influence of a previously reported dissolution process of UCNPs in aqueous solutions on the spectroscopic properties of exemplarily chosen Yb, Tm codoped nanocrystals. These results were then utilized to identify several upconversion emission bands that can be used as a screening parameter for the long-term stability monitoring of UCNPs.