Techn. Hochsch., Diss., 2003--Aachen.

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Dans le circuit primaire des réacteurs nucléaires à eau pressurisée, le bore participe au contrôle des réactions de fission. Le traitement de cette solution génère des déchets aqueux contenant une forte concentration en bore (de 1 à 3 mol/L). Le conditionnement de ces déchets à l'aide d'un ciment silico-calcique est compliqué par le fort pouvoir retardateur des ions borate sur l'hydratation du liant. Un traitement des déchets à la chaux est nécessaire pour précipiter les ions borate sous forme d'hexahydroborite. Cette stratégie, si elle limite le retard d'hydratation, ne le supprime pas. Par ailleurs, l'hexahydroborite est instable en milieu cimentaire et se convertit dans le temps en boroaluminate de calcium. Une autre approche pourrait consister à utiliser un ciment sulfoalumineux bélitique à forte teneur en ye'elimite. Ce liant présente en effet l'avantage de former en quantité importante des phases de type AFm et/ou AFt lors de son hydratation, phases qui peuvent incorporer des ions borate dans leur structure.Au cours de ce travail, l'hydratation de ciments sulfoalumineux par des solutions de borate de sodium a été étudiée au jeune âge et à plus long terme (sur une durée de 2 ans) dans l'objectif de préciser l'influence d'un ensemble de paramètres (pH du déchet, concentration en bore, taux de gypse du ciment) sur la vitesse d'hydratation du liant, la nature des hydrates formés, et les propriétés du matériau obtenu (résistance mécanique, stabilité dimensionnelle). Pour ce faire, une démarche analytique, procédant par complexification progressive des systèmes étudiés, a été mise en œuvre. Ainsi ont été successivement abordées la spéciation du bore en solution alcaline, l'étude des phases précipitant au sein des systèmes {CaO, B2O3, Na2O, H2O}, {CaO, B2O3, Al2O3, H2O} et {CaO, Al2O3, B2O3, SO3, H2O}, puis celle des pâtes de ciment gâchées avec une solution boratée simulant le déchet. L'approche expérimentale a été complétée par des modélisations thermodynamiques s'appuyant sur une base de données spécialement développée pour les besoins de l'étude.Il apparaît que le gypse joue un rôle primordial dans le contrôle de la réactivité du ciment. L'ajout de gypse fixe, par un mécanisme indirect, le pH de la solution interstitielle à une valeur proche de 11, ce qui favorise la précipitation transitoire d'un composé boraté faiblement cristallisé, l'ulexite. La dissolution des phases anhydres du ciment est alors fortement ralentie jusqu'à l'épuisement du gypse, conduisant ainsi à des retards de prise considérables. En l'absence de gypse, le retard à l'hydratation est de plus faible amplitude. Dans ces conditions, le pH de la solution interstitielle atteint des valeurs plus élevées, ce qui permet de déstabiliser rapidement l'ulexite. A plus long terme, les ions borate sont incorporés au sein d'une phase de type AFt, en solution solide avec les ions sulfate. Les résultats obtenus permettent de conclure que ce sont les ciments sulfo-alumineux contenant une faible teneur en gypse qui sont les plus adaptés au conditionnement de solutions à forte concentration en bore. / In the primary circuit of pressurized water reactors, boron helps controlling the fission reactions. The treatment of this solution produces aqueous low-level or intermediate-level and short lived radioactive with a high boron concentration (up to 1 to 3 mol/L). Stabilization/solidification of such wastes with calcium silicate cement is complicated by the strong retarding effect of borate ions on cement hydration. A calcium hydroxide addition is required to precipitate borate ions into hexahydroborite. With this approach, the hydration delay is limited, but not suppressed. Besides, hexahydroborite is unstable in the cement paste and is progressively converted into a hydrated calcium boroaluminate phase. Another strategy may consist in using belite calcium sulfoaluminate cement with high ye'elimite content. During hydration, this binder forms indeed large amounts of AFm and/or AFt phases which can incorporate borate ions into their structure.In this work, hydration of calcium sulfoaluminate cement by borated solutions was investigated at early age, and over a 2-year period, in order to determine the influence of a set of parameters (boron concentration and pH of the waste, gypsum content of the cement) on the hydration rate of the binder, on the phase assemblage formed, and on the properties of the resulting material (mechanical strength, volume change). An analytical approach was adopted, based on a progressive increase in the complexity of the investigated systems. The focus was successively placed on the speciation of boron in alkaline solution, on the study of the phases formed within the {CaO, B2O3, Na2O, H2O}, {CaO, B2O3, Al2O3, H2O} and {CaO, Al2O3, B2O3, SO3, H2O} systems, and on the characterization of cement pastes prepared with a borate solution which mimicked the waste. The experimental approach was completed by thermodynamic modelling using a database specially developed for the needs of the study. Gypsum appears to play a key role in controlling the reactivity of cement. The gypsum addition sets, by an indirect mechanism, the interstitial solution pH at a value close to 11, which promotes the precipitation of a poorly crystallized borated compound, ulexite. Dissolution of the anhydrous phases is strongly slowed down until the exhaustion of gypsum, and major delays are observed. Without any gypsum, the hydration delay is shorter. Under these conditions, the pore solution pH reaches higher values after mixing. Ulexite is consequently quickly destabilized. Borate anions are then incorporated into a mixed borate/sulphate AFt type phase. It appears that calcium sulfoaluminate cements with low gypsum contents should be recommended to solidify borated solutions.

No description available.

Poly(azolyl)borate ligands have proven to be extremely popular ligands since their introduction by Trofimenko in the late 60´s. The basic skeleton of these ligands involves usually three heterocycle units linked to a central boron apex via the azole nitrogen atoms. These ligands have been applied in diverse research areas such as homogeneous catalysis, materials science and bio-inorganic chemistry. More than 2000 papers, including books and reviews regarding the properties of these compounds, have been published. However, only a few synthetic methods for the preparation of such ligands have been reported and only a few examples of chiral borate-centred ligands are known. This thesis deals with the development of a novel synthetic route to tripodal borate ligands using B(NMe2)3 as the boron source. The mechanism of the reaction of this borane with azole heterocycles has been established by exploring the reactivity of a range of azoles. One of the major features of this new synthetic protocol is that it allows the formation of chiral tripodal ligands where the chiral groups are located either at the forth position at the boron atom or at the azole heterocycles. Coordination studies of the ligands have been undertaken and the metal complexes have been studied by a combination of spectroscopic and X- ray diffraction techniques. Preliminary application of the most representative ligands in the Asymmetric Transfer Hydrogenation (ATH) of prochiral ketones has been undertaken in collaboration with Prof. Dieter Vogt at the Technical University of Eindhoven.

Le sujet de la thèse initié dans le cadre de l'ANR UV-Borate s'inclut dans le projet UV-Conversion labellisée par 2 pôles de compétitivité (Matériala - Lorraine - et Route des lasers - Aquitaine -) soumis à l'ANR en 2011. Les études se portent particulièrement sur les borates YxLaySc4-(x+y)(BO3)4 (LYSB) et YAl3(BO3)4 (YAB), cristaux Optiques Non Linéaires (ONL) possédant la même structure cristallographique (R32). La croissance de ces cristaux est effectuée par les collaborateurs industriels et universitaires de l'ANR. Ces deux matériaux présentent en effet des possibilités de conversion de fréquence jusqu'à des longueurs d'onde λ < 300 nm, de plus une non hygroscopicité procure une plus grande durée de vie des échantillons et par conséquent un net intérêt pour les applications industrielles. L'endommagement laser étant lié à l'absorption et ainsi, en partie, aux impuretés, une étude de la qualité cristalline et de l'homogénéité de nos cristaux a été effectuée. Les résultats ont permis de relier des défauts de structure (dislocations et etch pits) à la croissance de la maille rhomboédrique via des caractérisations par ombre portée (Photography Schlieren) et par attaque chimique suivi d'une observation par microscopie optique, MEB et MFA. Par ailleurs, des études théoriques et expérimentales d'accord de phase (détermination de Θ et φ) lors de conversions de type I principalement ont été réalisées sur les cristaux de YAB, LYSB ainsi que sur des cristaux de référence tel que ß-BaB2O4 (ß-BBO). L'aspect de l'endommagement laser dans les matériaux ONL a été abordé dans les locaux de l'Institut Fresnel de Marseille au sein de l'équipe Interaction Laser Matière (ILM) sur des échantillons de Li2B4O7 (LTB). L'équipe a effectivement développé un dispositif de mesure de la probabilité d'endommagement laser et de mesure de tenue du seuil d'endommagement laser des matériaux optiques. Par ailleurs, un effort a été mené dans la conception d'un dispositif de mesure de la transmission optique et absorption à température ambiante et aux basses températures afin de révéler des défauts absorbants. Des premiers résultats ont été obtenus et discutés sur des échantillons de ß-BBO et LYSB / The purpose of my thesis, performed within the program of the ANR UV-Borate, was integrated in the UV-Conversion project certified by 2 poles of competitiveness (Matériala - Lorraine - and Route des lasers - Aquitaine -). The project concerned the study of borates YxLaySc4-(x+y)(BO3)4 (LYSB) and YAl3(BO3)4 (YAB), Non-Linear Optical (NLO) crystals which have the same crystallographic structure (R32). The growth of the crystals was realized by industrials and academics collaborators of the ANR. Those two materials present possibilities of frequency conversion until wavelengths λ < 300 nm. Because they are not hygroscopic, they have a bigger time life compare to other materials which offer a most important interest for the industrial applications. We have studied the quality and the homogeneity of our crystals. Indeed, the use of strong optical beam can lead to damages on the crystal and degrade the properties of the materials which are related to the absorption and to impurities of the crystals. Our results allowed to related defaults in the structure (dislocations and etch pits) to the growth of the rhombohedral crystal system by using characterization techniques as the "Photography Schlieren" or optical microscopy (before which a "Chemical Etching" was performed) or by using SEM and AFM. In the fridge of the previous work, theoretical and experimental phase matching studies (determination of Θ and φ) during conversions of frequency of type I were realized on the YAB and LYSB crystals and on the reference crystals such as ß-BaB2O4 (ß-BBO). The aspect of optical damage was investigated at the Institut Fresnel of Marseille in the team Intéraction Laser Matière (ILM). The team has developed a device to measure the Laser Induced Damage (LID) probability and to measure of the Laser Induced Damage Threshold (LIDT) of optical materials. Laser-Induced-Damages studies in NLO materials were also realized on Li2B4O7 (LTB) samples. A strong effort was performed in the design of a device for the measurement of the optical transmission and the absorption at room temperature and low temperatures to reveal absorbent defaults. First state-of-art results were obtained and discussed for ß-BBO and LYSB samples

Vidros boratos contendo óxidos modificadores vêm sendo estudados por apresentarem um número atômico efetivo próximo ao do tecido humano, o que os tornam materiais interessantes para o desenvolvimento de dosímetros termoluminescentes. O objetivo deste trabalho foi estudar as propriedades térmicas e estruturais do sistema xCaB4O7-(100-x)CaB2O4, com x variando de 0 a 100 % em massa. As amostras sem dopantes foram previamente estudadas a fim de determinar uma composição que apresentasse a melhor resposta termoluminescente (TL) para a inclusão do íon Dy como dopante e Li como co-dopante, aumentando a eficiência TL da mesma. Pelo método de fusão e moldagem, foram obtidos amostras vítreas e vitrocerâmicas. A fase cristalina presente nas amostras vitrocerâmicas foi determinada por difratometria de raios X e identificada como fase única CaB2O4. A composição vitrocerâmica 20CaB4 (% em massa) apresentou a melhor resposta TL, sendo dopada com Dy e co-dopada com Li para o estudo das propriedades dosimétricas. Este estudo mostrou uma resposta linear num intervalo de 5 a 70 minutos de exposição à radiação ultravioleta e uma boa reprodutibilidade do sinal TL provando ser um material promissor para a utilização em dosimetria pessoal e clínica. / Borate glasses containing modified oxides have been studied on account of their effective atomic number close to that of the human tissue, what makes them interesting materials for the development of the thermoluminescent dosimeters. The purpose of this work was to study the thermal and structure properties of the xCaB4O7-(100-x)CaB2O4 system with x ranging from 0 to 100 wt%. The undoped samples were previously studied in order to determine a composition that would present a better thermoluminescent response for the incluision of the Dy íon as dopant and Li as co-dopant, thus increasing its TL efficiency. By the melting/molding method, the glass-ceramic samples was determined by the X-ray difractometry and identified as a unique CaB2O4 phase. The glass-ceramic 20 CaB2O4 (wt%) composition presented the best TL response being doped with Dy and co-doped with Li for the study of the dosimetric properties. This study has shown a linear response within an interval of 5 to 70 minutes of exposure to the UV radiation and good reproducibility of the TL signal, thus proving to be a promising material for using in the personal and clinical dosimetry.