Este trabalho apresenta um estudo dos mecanismos de transporte iônico nos vidros fluorsilicatos de cádmio e chumbo de composição 40SiO2 40PbF2 20CdF2, e nos vidros boratos contendo LiF de composição 50B2O3 10PbO 40LiF. Estes materiais são importantes pela sua potencial utilização em dispositivos ópticos e eletrólitos sólidos. No vidro borato 50B2O3 10PbO 40LiF o estudo da forma de linha do 7Li mostrou que esta é influenciada tanto por interações dipolares quanto por quadrupolares. O estudo de RMN revelou que há dois F- presentes neste vidro, um deles em vizinhaças de Pb (F- incorporados à rede vítrea substituindo o oxigênio do grupo PbO), e o outro em vizinhanças de Li. A forma de linha de RMN dependente da temperatura para o lítio e para o flúor, e seus tempos de relaxação, exibem as características qualitativas associadas com a alta mobilidade do 7Li e do 19F neste sistema. Este estudo também mostrou que, neste vidro, tanto o Li+ como o F- contribuem para a condutividade medida, sendo que o 7Li é móvel a temperaturas mais baixas (a partir de 250 K), e o 19F começa a se mover em temperaturas mais altas (a partir de 400 K). No vidro 40SiO2 40PbF2 20CdF2, os resultados de RMN mostraram a alta mobilidade do flúor e evidenciaram duas dinâmicas diferentes dos íons flúor. Os dados da relaxação do flúor revelaram um máximo da taxa de relaxação spin-rede abaixo da temperatura de transição vítrea (Tg), indicando que a mobilidade do flúor, neste vidro, é comparável àquelas encontradas em condutores iônicos rápidos / This work presents a study of the ionic transport mechanisms in lead-cadmium fluorosilicate glasses, of composition 40SiO2 40PbF2 20CdF2, and in borate glasses containing LiF, of composition 50B2O3 10PbO 40LiF. These materiais are important due to theirs high potential applicability in optic devices and in solid electrolytes. In the borate glass 50B2O3 10PbO 40LiF, the line shape study of 7Li shows an influence of the dipolar and quadrupolar interactions. The NMR results showed that there are two kinds of F- ions in this glass, one in the Pb vicinity (F- in the glass lattice, in substitution of the PbO oxygen), and the other in the Li vicinity. The NMR line shape depends on the temperature for the 7Li and 19F atoms, and their relaxation times reflect qualitative features related to the high mobility of there nuclei. Also, this study shows that, in this glass, both, 7Li and 19F, play an important role in the electric conductivity. The 7Li is mobile for low temperatures (from 250 K), while the 19F is mobile for high temperatures (from 400 K). In the 40SiO2 40PbF2 20CdF2 glass, the NMR results showed the high mobility of the fluorine ions, indicating two different dynamics of those nuclei. The relaxation data of the 19F presented a spin-lattice relaxation rate maximum below the glass transition temperature (Tg, indicating that the 19F mobility in this glass is comparable to that of rapid ionic conducting glasses

Vidros são materiais atraentes do ponto de vista científico e tecnológico, em especial porque algumas composições químicas permitem a fabricação em larga escala e/ou podem apresentar propriedades físico-químicas que os tornam candidatos promissores para aplicações como meio ativo para lasers, filtros ópticos, fibras ópticas, blindagens mecânicas ou como objeto de decoração ou utensílios domésticos ou como elemento para a construção civil, entre outras. Um dos desafios em preparar novas composições de materiais vítreos é garantir que não apareça o fenômeno da devitrificação. Este trabalho foi realizado com o objetivo de preparar e caracterizar uma nova matriz multicomponente, a base de óxido de boro, livre do fenômeno de cristalização. A matriz [50B2O3 - 15ZnO - 10PbO - 8MgO - 6K2O - 2Al2O3 - 2Nb2O5 - 5Si2O - 2Na2O] %wt pura e dopada com 0,1% mol de íons de metais de transição (MnO2, Fe2O3, CoO, NiO, CuO e CdCl2), foram preparadas em forno elétrico de atmosfera aberta usando cadinho de platina e caracterizadas usando as técnicas de: difração de raios X, análise térmica, densidade, pelo princípio de Arquimedes, microdureza Vickers, colorimetria, absorção óptica no intervalo ultravioleta-vísivel (UV-Vis) e transmissão óptica na região do infravermelho (FTIR). Resultados de difração de raios X confirmaram o caráter não cristalino das amostras vítreas. A adição de dopantes levou a mudança no número de coordenação na rede borato. Resultados de absorção óptica evidenciaram que a nova matriz desenvolvida com a adição de íons de metais de transição absorvem na região do visível e infravermelho próxima. Esses vidros tem potencial de aplicação na indústria de produtos decorativos e como filtros ópticos. / Glasses are attractive materials on a scientific and technologic point of view especially because some of their chemical compositions can provide a large scale production and/or may present physicochemical properties that them become promising candidates for applications as laser active environments, optical filters, optical fibers, mechanical shielding, adornment, domestic tools or construction stuff, among others. One of the challenges in preparing new compositions of glassy materials is to ensure that does not appear the phenomenon of devitrification. This work was carried out in order to prepare and characterize a new multicomponent glassy matrix, the basis of boron oxide, free from crystallization phenomenon. Pure glassy samples of [50B2O3 - 15ZnO - 10PbO - 8MgO - 6K2O - 2Al2O3 - 2Nb2O5 - 5Si2O - 2Na2O % wt] and 0.1% mol of transition metal ions (MnO2, Fe2O3, CoO, NiO, CuO e CdCl2) doped were prepared in open atmosphere electric furnace using platinum crucible and characterized using x-ray diffraction, thermal analysis, density evaluation from Archimedes principle, Vickers microhardness measurements, colorimetry, UV-VIS optical absorption and IR optical transmission. X-ray diffraction results confirmed non-crystalline character of the vitreous samples. Dopants addition led to changing on the coordination number of the borate network. Optical absorption results showed that the new glassy matrix developed with addition of transition metal ions absorb in the visible and near infrared range. These glasses may have potential applications in decorative products and as optical filters.

L'ion ytterbium trivalent présente la particularité de pouvoir donner lieu à deux émissions aux propriétés spectroscopiques différentes : l'une, de durée de vie courte, dans l'ultraviolet (émission de transfert de charge) employée au sein de détecteurs tels que les scintillateurs, et l'autre, de durée de vie longue, dans l'infrarouge (émission de type 4f x 4f) pour des applications de type laser.La relation étroite qui existe entre structure et propriétés de la matière est illustrée au travers de l'étude de la luminescence de l'ytterbium, dans l'ultraviolet et l'infrarouge, inséré dans le borate Li6Y(BO3)3 ainsi que deux oxyborates : LiY6O5(BO3)3 et Y17,33B8O38. Pour la première fois dans des oxyborates une émission de transfert de charge de l'ytterbium a été observée. Une approche théorique a permis le calcul des courbes à une seule coordonnée de configuration des niveaux d'énergie de la liaison ytterbium - oxygène, ainsi que la simulation de l'extinction thermique de cette émission. L'étude de la spectroscopie infrarouge de l'ytterbium dans ces composés a été réalisée et une attribution des niveaux d'énergie est proposée dans le cas du borate Li6Y(BO3)3 : Yb3+. Une approche originale est également introduite avec l'étude des états de transfert de charge pour les trois composés via l'émission dans l¤infrarouge. Les premiers tests portant sur les performances lasers dans trois régimes de fonctionnement (continu, déclenché et blocage de modes) d¤un cristal de Li6Y(BO3)3 : Yb3+ (Yb-LYB) sont reportés.

Graduation date: 1993

The primary objective of this study was to investigate mould growth resistance of different types of wood products which include the sheathing and framing within full scale wall assemblies. Secondary objectives were to investigate the difference in mould growth resistance between borate-treated and untreated wood products as well as provide information about mould growth under different temperature and humidity conditions for treated and untreated wood products. <br /><br /> The objective of the study is to better understand mould growth, and to examine the effects of varying high moisture conditions on wooden products and the mould growth which may result. More importantly this will be examined on full scale wall assemblies; to date mould growth studies have only been performed within a laboratory on small samples of materials. Moreover, this study recreates the conditions which evidently cause mould growth on full scale wall assemblies. Tests were performed within a climate chamber on three full scale wall assemblies. The original scope of this study included an examination of the sheathing and framing components within a full scale wall assembly, however this study will focus mainly on the sheathing. <br /><br /> Results of this study indicate that the relative humidity conditions needed for mould growth on wood are higher than originally believed (i. e. , significantly greater than 80%RH). During the first eight weeks of test number one the relative humidity at the surface of the sheathing was held constant at 95% and little mould growth was observed on the untreated sheathing (mould growth index of 3 or less); little or no mould growth on the treated sheathing (mould growth index of 1 or less). The second and third tests demonstrated that the presence of liquid water greatly accelerated the time to germinations, the amount of mould growth (up to a mould growth index of 6), and the rate of mould growth. All three tests clearly showed that borate-treatment reduced the amount of mould growth; however, the concentration of borate-treatment, and the types of materials treated, does affect the resistance of mould growth. Furthermore, there was some evidence to suggest Borate treatments of the plywood increased the time to germination significantly, from a few weeks to 16 weeks in this study, but once mould growth was initiated, the rate of mould growth was similar to that of the untreated plywood. Two mathematical models to determine mould growth were examined: Viitanen and WUFIBIO (Sedlbauer). Viitanen?s model predicted time to germination and rate of growth rate well for untreated plywood, and WUFIBIO predicted time to germination but not the growth rate. It was also found both models err on the side of caution in predicting mould growth. <br /><br /> Recommendations include improvements to the test method and producers, and for future work.

In drilling technologies, Na-bentonite-water mixtures are used as drilling mud. As the reserves of sodium-bentonite decline, calcium or low-quality bentonites are activated with inorganic salts and/or treated with different types of polymers as an alternative to Na-bentonite. The quality of such bentonites, commonly referred to as extended bentonite may deteriorate under severe drilling conditions, such as / bacterial activity, high temperature etc. It was considered that borates could prevent the deterioration of extended bentonites due to their well known bactericide properties. This study involves the use of Na-Borate as an activating agent for bentonites in place of the commonly used Na-carbonate. The effects of Na-borate on the rheological and filtrate behaviours of two different bentonites, namely, Edirne Bentonite (E-Ben) and &Ccedil / ankiri Bentonite (C-Ben) were investigated. The results were evaluated based on API standards and in comparison to those of Na-carbonate activated bentonites. It was found that Na-borate could be used as a bentonite activator, although somewhat higher dosages (3,78% Na2O equivalent for E-Ben and 0,76% Na2O equivalent for C-Ben) than Na-carbonate (2,90% Na2O equivalent for E-Ben and 0,58% Na2O equivalent for C-Ben) are necessary to obtain the same rheological properties. In terms of aging, it was determined that aging had no adverse effect on v the rheological and filtrate properties of bentonite treated with carboxymethyl cellulose (CMC) and polyanionic cellulose (PAC), but rheological properties of bentonites treated with xanthan gum were found to deteriorate upon aging. The presence of Na-borate in the mud appears to alleviate this adverse effect.

This thesis addresses the application of xanthan/borate gel for lost circulation treatment. Steady shear viscometry method was applied in which the gel system was under constant shear rate while apparent viscosity was being recorded. The apparent viscosity was constant up to initial gelation time in which viscosity started to build up. Four parameters: initial and final gelation times as well as initial and final viscosities are defined and a correlation is derived between those parameters and four variables: polymer blended with crosslinker, pH-controller, and magnesium chloride concentration as well as temperature. These correlations can help the drilling industry to manage the lost circulation treatment job in a way to have enough time and pressure to pump the fluid and to optimize the time and quality required for final gel. The effects of those variables besides mixing time and shear history on gelation were also investigated. Temperature and pH-controller shortens initiation of gelation. Poly-cross shifts viscosity upward. Retarder postpones the final gelation time. Shear history does not affect initial gelation time and increase of mixing time reduces initial gelation time. This thesis also investigates the rheological model behavior of this gel system before initial gelation time which is the time allowed for pumping the fluid. Shear stress was measured at 0.1,1,50, and 450 rpm besides the conventional readings. Then residual mean squares for six common rheological models were obtained. Sisko was found to be the best fitting model based on this statistical approach. Moreover a modified Bingham-plastic and low shear yield point model are suggested.

The objectives of this study are to synthesize sub-micron sized zinc borate and to use them with other flame retardant additives in poly(ethylene terephthalate) (PET) based composites. The study can be divided into two parts. In the first part, it was aimed to synthesize sub-micron sized zinc borate (2ZnO.3B2O3.3.5H2O) with the reaction of zinc oxide and boric acid. For this purpose, low molecular weight additives or surfactants were used in the syntheses to prevent the agglomeration and to decrease particle size. Effect of type of surfactant and its concentration / effect of using nano-sized zinc oxide as reactant on the synthesis, properties and morphology of 2ZnO.3B2O3.3.5H2O were investigated. Synthesized zinc borates were characterized by X-Ray diffraction (XRD), Scanning Electron Microscope (SEM) and Thermogravimetric Analysis (TGA). The results were compared with a commercial zinc borate, Firebrake (FB). Characterization results showed that at least in one dimension sub-micron size was obtained and synthesized zinc borates did not lose their hydration water until the process temperature of the composites. In the second part of the study, PET based composites, which mainly included synthesized sub-micron sized zinc borates were prepared by using a co-rotating twin screw extruder and injection molding machine. Synergist materials such as boron phosphate (BP) and triphenyl phosphate (TPP) were also used in the composite preparation. The composites were characterized in terms of flammability and mechanical properties. Flammability of composites was determined by using a Limiting Oxygen Index (LOI) test. Mechanical properties such as tensile strength, elastic modulus, elongation at break and impact strength were also studied. According to LOI and impact tests, the composites containing 3 wt. % BP and 2 wt. % zinc borate which was modified with poly(styrene-co-maleic anhydride), 2PSMA05/3BP and 2PSMA1/3BP have higher LOI and impact values when compared to neat PET.

Thesis (Ph. D.)--West Virginia University, 2003. / Title from document title page. Document formatted into pages; contains xi, 124 p. : ill. (some col.). Includes abstract. Includes bibliographical references (p. 81-87).

Zinc borate is a flame retardant additive used in polymers, wood applications and textile products. There are different types of zinc borate having different chemical composition and structure. In this study, the production of zinc borate that had the molecular formula of 2ZnO.3B2O3.3,5H2O was studied. The aim of this study was to investigate the effects of reaction parameters on the properties of zinc borate that had been synthesized by the reaction of boric acid and zinc oxide at the existence of the seed crystals and to determine the optimum experimental conditions for zinc borate production reaction. Reaction kinetics was also investigated to find a suitable kinetics model. The effect of boric acid to zinc oxide ratio -H3BO3:ZnO ratio- (3:1, 3.5:1, 5:1 and 7:1), the particle size of zinc oxide (10&micro / m and 25&micro / m), stirring rate (275 rpm, 400 rpm, 800 rpm and 1600 rpm), temperature (75&deg / , 85&deg / and 95&deg / ) and size of seed crystals (10&micro / m and smaller size) on reaction rate, reaction completion time, composition and particle size distribution of zinc borate were investigated. Experiments were performed in a continuously stirring, temperature controlled batch reactor with a volume of 1.5L. During the experiments samples were taken to be analyzed in regular time intervals. The analyses of the samples gave the concentration change of zinc oxide and boron oxide in the solid as well as the conversion of zinc oxide to zinc borate with respect to time and the rate of reaction was calculated. The products were also analyzed for particle size distribution. The experimental results showed that the reaction rate increased with the increasing H3BO3:ZnO ratio, particle size of zinc oxide, stirring rate and temperature. The reaction completion time was also decreased by increasing H3BO3:ZnO ratio, stirring rate and temperature. The particle size of final product, zinc borate, decreased with increasing stirring rate and size of zinc borate used as seed and increased with increasing particle size of zinc oxide used as reactant. The average particle sizes of the final product zinc borates synthesized at the end of the experiments were ranged between 4.3 &micro / m and 16.6 &micro / m. The zinc borate production reaction was mainly fitted the unreacted core model for the case of diffusion through product layer controls.