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Glass forming ability, structure and spectroscopic properties of silica-free calcium aluminate based glasses.Uhlmann, Eugenie Victoria. January 1995 (has links)
Calcium aluminate based glasses are interesting because of their unusual optical properties and the fact that they do not contain any traditional glass forming ions. A large focus of the glass literature has been concerned with the study and properties of typical glass forming ions. For this reason, comparatively little is known about the possibility of glass formation and the structure and properties in unusual systems. The present work will describe the limits of glass formation within the calcium aluminate system. The use of non-silicate based stabilizing additives will also be detailed. It has been demonstrated that certain additions to the calcium aluminate system will improve the glass formation tendency without impairing the desired optical properties. The effects of various ions and their impact on the processing and properties of the glasses will be described in the framework of traditional theories of glass formation. Additional optical properties of the calcium aluminate system have also been investigated. Using the Judd-Ofelt model, various spectroscopic properties of calcium aluminate based glasses have been calculated. The stimulated emission cross section, branching ratios, intensity parameters and transition probabilities show interesting variations with compositional manipulations. Attempts to improve the emission cross section will also be described. The structure of calcium aluminate based systems has been studied using NMR and Raman Spectroscopy. The coordination of alumina has been examined with respect to compositional changes. In addition, structural studies have been conducted on calcium aluminate glasses synthesized by the sol-gel method. This method has allowed the formation of higher alumina content glasses. The evolution of structure with heat treatment temperature was followed and a comparison between melt-derived and sol-gel prepared glasses has been made.
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Early-age behavior of calcium aluminate cement systemsIdeker, Jason Henry, January 1900 (has links)
Thesis (Ph. D.)--University of Texas at Austin, 2008. / Vita. Includes bibliographical references.
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TThe (O?H?)?? tetrahedron in tricalcium aluminate hexadeuterate determined by means of neutron and X-ray diffraction /Foreman, Dennis Walden January 1966 (has links)
No description available.
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Calcium Aluminates Synthesis, Characterization, and Hydration BehaviorGriffin, Joseph George 12 1900 (has links)
The hydration behavior of the calcium aluminates as a function of the glass content, the curing temperature, and the water-solid ratio was investigated. In order to keep them from influencing the results, the free-lime content and the surface area of all samples were kept constant, whenever possible. Samples were hydrated with a water-solid ratio of 10/1 for periods of 1 to 90 days. Three curing temperatures were studied; 2°C, 25°C, and 50°C. Samples were hydrated in tightly sealed polyethylene containers to prevent reactions with atmospheric carbon dioxide. The hydration was followed by X-ray diffraction and thermal analysis. Only two samples, Hexacalcium Tetra-alumino Magnesium Silicate and Tricalcium Magnesium Dialuminate, were successfully prepared in an amorphous form. These compounds were used to investigate the effect of glass content on the hydration behavior. Results indicate that when the glass content is increased a corresponding increase is found in the percent combined water. Samples hydrated at 25°C were influenced by changes in the glass content to a greater degree than were those hydrated at either 2°C or 50°C. The effect of the water-solid ratio on the hydration behavior of the calcium aluminates was studied using the compounds; Hexacalcium Tetra-Alumino Magnesium Silicate/ and Dodecacalcium Hepta-Aluminate. In general, samples that were hydrated with large water-solid ratios reacted more completely than did those hydrated with small water-solid ratios. The presence of sufficient water to theoretically hydrate the samples to completion did not guarantee that the sample would do so. The curing temperature influenced the hydration behavior to a greater degree than did the glass content or the water-solid ratio. Increasing the curing temperature not only increased the rate of hydration, but, in some cases, also changed the hydration products.
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The Synthesis and Crystal Chemistry of Ca12Al14O33 doped with Fe2O3Ude, Sabina Nwamaka 01 August 2010 (has links)
The crystal chemistry of Fe doped mayenite (Ca12Al14-xFexO33) samples prepared using solid state and sol-gel synthesis techniques were compared. Five samples were prepared using solid state process with varying Fe concentration (x) where x = 0, 0.05, 0.1, 0.25 and 0.3; two sets of samples were made via the sol-gel, the first set was prepared for studying the amount of Fe substituted by varying the Fe concentration where x = 0, 0.05, 0.1, 0.2, 0.3 and 0.4 and the second set was prepared for studying the firing temperature and did not contain Fe additions (x = 0). Samples produced via the sol-gel method were more likely to be single phase with incorporation of Fe2O3 while solid state samples contained multiple phases over the same range of Fe2O3 substitutions. The refined lattice parameters, of samples prepared using both methods were observed to increase with increasing Fe concentration, suggesting Fe is replacing Al since Fe has larger ionic radii than Al. Samples prepared via the sol-gel method were found to be single phase at lower temperatures compared to samples prepared via solid state synthesis. Samples synthesized using the sol-gel method were found to have multiple phases when fired at 800 ˚C but were single phase when fired at 900˚C. In comparison, samples synthesized using traditional solid state techniques showed single phase when fired at a temperature of 1350˚C.
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The Synthesis and Crystal Chemistry of Ca12Al14O33 doped with Fe2O3Ude, Sabina Nwamaka 01 August 2010 (has links)
The crystal chemistry of Fe doped mayenite (Ca12Al14-xFexO33) samples prepared using solid state and sol-gel synthesis techniques were compared. Five samples were prepared using solid state process with varying Fe concentration (x) where x = 0, 0.05, 0.1, 0.25 and 0.3; two sets of samples were made via the sol-gel, the first set was prepared for studying the amount of Fe substituted by varying the Fe concentration where x = 0, 0.05, 0.1, 0.2, 0.3 and 0.4 and the second set was prepared for studying the firing temperature and did not contain Fe additions (x = 0). Samples produced via the sol-gel method were more likely to be single phase with incorporation of Fe2O3 while solid state samples contained multiple phases over the same range of Fe2O3 substitutions. The refined lattice parameters, of samples prepared using both methods were observed to increase with increasing Fe concentration, suggesting Fe is replacing Al since Fe has larger ionic radii than Al. Samples prepared via the sol-gel method were found to be single phase at lower temperatures compared to samples prepared via solid state synthesis. Samples synthesized using the sol-gel method were found to have multiple phases when fired at 800 ˚C but were single phase when fired at 900˚C. In comparison, samples synthesized using traditional solid state techniques showed single phase when fired at a temperature of 1350˚C.
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Multi-scale characterization, implementation, and monitoring of calcium aluminate cement based-systemsBentivegna, Anthony Frederick 03 July 2012 (has links)
Calcium aluminate cement (CAC) is a rapid hardening cementitious material often used in niche concrete repairs where high early-age strength and robust durability are required. This research project characterized the implications of the additions of various mineral and chemical admixtures to plain CAC to mitigate strength reductions associated with conversion, an inevitable strength reduction associated with the densification of metastable hydrates (CAH10 and C2AH8) to stable hydrates (C3AH6 and AH3). The effect of these admixtures on early-age strength development, volume change, and the correlation to macro-scale performance were reported in this dissertation. Various mixtures of CAC were investigated including: pure CAC, binary blends of CAC with fly ash (Class C) or CaCO3, and ternary blends of CAC with slag and silica fume. Characterization of the influence of these admixtures on hydration was completed using x-ray diffraction, isothermal calorimetry, and chemical shrinkage. Investigations on the implications of early-age volume change were conducted for autogenous deformation. In addition to laboratory testing, the final phase of the project was to correlate and elucidate the data generated in the laboratory to real-world field performance. Field trials were conducted to evaluate and monitor the behavior of CAC systems and investigate the link between laboratory generated research and actual large scale behavior. / text
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Calcium-Aluminate as Biomaterial : Synthesis, Design and EvaluationLööf, Jesper January 2008 (has links)
<p>In this thesis different aspects of calcium-aluminate (CA) as biomaterial are presented. Calcium aluminate is a chemically bonded ceramic with inherent properties making it suitable for use as biomaterial in some applications. In this thesis the emphasis is put on the basic chemical, physical and mechanical properties that may be achieved using the CA system as well as synthesis of the CA raw material. The basis for using CA in any application is the synthesis of the raw material. Different synthesis routes for producing CA are presented with focus on high temperature routes and the micro-structural and phase development during synthesis. As a base for further understanding of the CA properties a thorough outline of the reaction chemistry for CA is presented also including a description of how the reactions may be controlled and how formulations can be designed. The surface reactions of CA when subjected to simulated body fluid showed that CA is <i>in vitro</i> bioactive. An <i>in vivo</i> study in teeth also indicates that CA produces apatite at the tooth material interface. Dental materials are subjected to a harsh environment in the mouth with high mechanical forces, erosion and thermal changes. Also the demands on precise handling characteristics are high. For these reasons the <i>in vitro</i> evaluation of physical and mechanical properties are important. In this work several mechanical and physical properties of Ca-based formulations for dental applications has been tested using different methods. Some attention is also put on the specific characteristics of CA and the difficulties that arise when new material classes needs to be tested according to consensus standard methods. Finally studies on a CA-based formulation intended for Vertebroplasty is presented. The studies include basic mechanical properties as well as testing the material in an <i>in vitro</i> model utilising synthetic cancellous bone.</p>
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Preparação e caracterização de vidros aluminato de cálcio com baixa concentração de sílica dopados com Nd2O3 e Er2O3 / Physical properties of low silica calcium aluminate glasses doped with NdO3 e Er2O3Sampaio, Jurací Aparecido 11 October 2001 (has links)
O desenvolvimento de laseres de estado sólido compacto operando na região do infravermelho médio, entre 2 - 5 ?m, tem recebido considerável atenção nos últimos anos. Esses dispositivos oferecem grande potencial como fonte de luz para uma infinidade de aplicações, como por exemplo laseres para medicina e sensores químicos remotos. Laseres operando na região de 2.8 ?m tem interesse particular na medicina devido a forte banda de absorção da água nessa região espectral. Para se conseguir forte emissão laser próximo a 2.8 ?m têm sido investigadas famílias de vidros não-óxidos, como por exemplo vidros fluoretos de metais pesados e vidros chalcogenetos, dopados com Er3+. Entretanto esses vidros são caros, difíceis de serem feitos, além de serem tóxicos. Por essa razão o desenvolvimento de um vidro óxido seria ideal, já que são mais baratos, relativamente fáceis de serem produzidos, além de não serem tóxicos. A desvantagem dos vidros óxidos é a sua alta energia de fônons, quando comparada aos vidros haletos e chalcogenetos, que aumenta a taxa de transição não radiativa. Seria interessante investigar um sistema vítreo que tivesse propriedades otimizadas, ou seja, boas propriedades ópticas, térmicas e mecânicas, e baixa energia de fônons. O sistema vítreo aluminato de cálcio seria um candidato para essas aplicações, já que preenche essas exigências. Porém não há na literatura informações a respeito da influência de pequenas quantidades de elementos terras raras nas propriedades desses vidros, e qual é a concentração ideal desses íons. O objetivo dessa tese foi investigar composições de vidros aluminato de cálcio (48,1 CaO : 40.8 Al2O3 : 4.1 MgO : 7.0 SiO2) dopados com Nd2O3, Er2O3 ou Yb2O3, e verificar qual a influência desses íons nas propriedades ópticas, térmicas, mecânicas e termo-ópticas. Investigou-se também qual a influência da atmosfera de fusão. Com esse objetivo as amostras foram fundidas em cadinhos de grafite sob vácuo, e em cadinhos de platina, ao ar, ambas as fusões ocorreram a 1400 °C. As amostras foram investigadas através de difração de raios-X e microscopia óptica, cujos resultados confirmaram o estado amorfo das amostras preparadas. As amostras não apresentaram estrias e tiveram boa transparência óptica. Os espectros de transmitância mostraram que o processo de fusão a vácuo eliminou completamente a forte banda de absorção próxima a 3 ?m devida a água. O corte da transmitância na região do infravermelho ocorreu em 5.5 ?m, sendo independente do tipo do íon terra rara presente na composição do vidro. O índice de refração em 546.1 nm aumentou de 1.6702 (amostra base) para 1.6876 (amostra dopada com 8% de Er2O3). Este acréscimo no índice de refração é atribuído a um aumento da polarizabilidade eletrônica do vidro devido ao aumento de oxigênios nonbridging. A densidade aumenta de 2.92 g/cm3 (amostra base) para 3.12 g/cm3 (amostra dopada com 8% de Er2O3), esse aumento é explicado levando em consideração a massa dos átomos terras raras, que são maiores em relação ao Al2O3. A dureza dos vidros aluminato de cálcio diminuiu de 865 kg/mm2 (amostra base) para 781 kg/mm2 (amostra dopada com 8% de Er2O3), ou seja aproximadamente 11% de decréscimo. No caso da temperatura de transição vítrea, Tg, esse decréscimo é de aproximadamente 8%, sendo 841 °C para a amostra base e 782 °C para a amostra dopada com 8% de Er2O3. Para o vidro base, a difusividade térmica foi de 5.75 x 10-3 cm2/s e a condutividade térmica foi de 15.5 x 10-3 cm-1 K-1. Tanto a difusividade quanto a condutividade térmica decresceram na mesma proporção da dureza e Tg, conforme substitui-se a alumina pelo óxido terra rara. Esta é uma indicação de que os átomos terras raras atuam como modificadores de rede, abrindo a estrutura do vidro, diminuindo a resistência mecânica e atuando como barreiras térmicas no material. A resistência ao choque térmico dos vidros aluminato de cálcio é de 339 W/m, semelhante aos vidros silicatos que é de 358 W/m, e aproximadamente quatro vezes maior que a dos vidros fluoretos, 86 W/m. Este resultado confirma a hipótese de que os vidros aluminato de cálcio podem suportar variações abruptas de temperatura. Através da espectroscopia de lente térmica foram obtidas a eficiência quântica dos vidros aluminato de cálcio dopados com Nd2O3 e Er2O3. No caso das amostras dopadas com concentrações menores de 3% de Nd2O3 a eficiência quântica foi de aproximadamente 80%. Esses resultados indicam que os vidros aluminato de cálcio são excelentes candidatos para laseres de estado sólido e demais aplicações ópticas na região do infravermelho médio. / The development of compact solid-state lasers operating in the midinfrared wavelength region (2 -5 ?m) has been an area of considerable activity in the last few years. These devices offer great potential as light sources for applications as medical lasers as well as in remote chemical sensing devices. Light sources in the 2.8?m region are of particular interest for medical applications due to the strong water absorption in this spectral region. Apart from allowing extremely precise cutting and ablation of water-containing tissues, the other advantages of using light sources operating at 2.8 ?m are related to the possibilities of reducing skin burning in surgeries, decrease in the use of anesthesia and shortening of recovery time, especially in skin surgeries and in the cutting and remova1 of hard tissues, such as tooth enamel and bone. In order to achieve strong laser emission around 2.8 ?m the effort so far has been concentrated on the family of Er3+ doped non -oxide glasses such as heavy metal fluorides and chalcogenides. However the production of these glasses is expensive, and it is difficult to make them, besides they are toxic. On the other hand, the oxide glasses are cheaper, atoxic and easy to produce them. The disadvantaged, however, is its the relative high phonon energy that promote high nonradiative transition rates. Since calcium aluminate glasses are formed with non-network forms, CaO and Al2O3, they have high tendence towards devitrification. The addition of small amounts of alkali and alkaline earth elements enlarges the glass forming region. Several calcium aluminate glasses compostions containing SiO2, BaO and MgO are now reported in the literature. In this thesis, low silica calcium aluminosilicate glasses doped with Nd2O3 and Er2O3 were prepared. Since the sample compositions were close to the phase diagram glass formation, the rare earth doping was performed up to 8wt.%. The samples was melted under vacuum condition in a graphite crucible at 1500 °C, and in air in a platinum crucible. The influence of the rare earth doping on the thermal diffusivity, thermal conductivity and Vickers hardness was such that all these physical parameters decreased by roughly the same amount, namely 8%, between the undoped and 5 wt% of Nd2O3. The dependence of these parameters, as a function of the Nd2O3 doping, strongly supports the idea that the Nd3+ or Er3+ act as network modifiers. Elastic module (E, G, K, v) of calcium aluminosilicate glasses with < 10 mole% of SiO2 doped with Er2O3 and Yb2O3, melted in air and under vacuum conditions, have been measured using the pulse echo ultrasonic technique. There was a decrease of the elastic properties, about 5%, as rare earth doping increases from 0.2 to 1.5-mol% (about 8 wt%). The Young\'s modulus did not vary within errors of measurements. The Debye temperature varied between (369±9)K and 352±9 K, which is explained assuming that the rare earth ions acts as network modifiers disrupting the glasses structure. The undoped calcium aluminate glasses fracture toughness is (1.4±0.3) MPa m1/2 and the thermal shock resistance is (339±102) W/m. The fluorescence quantum efficiency determined by thermal lens spectroscopy, was found be about 80% for the 2wt% Nd2O3 doped calcium aluminosilicate glass. The fluorescence quenching was observed to doping higher than 2wt% Nd2O3. The variation of the refractive index as a function of the temperature, dn/dT, was found be 8.0 x 10-6/0c. Among the various glass system investigated, CA glasses presented greater mechanical properties and larger thermal shock resistance, indicating that these materials are candidates for solid state laser applications and other infrared applications.
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"Investigação do processo de obtenção de aluminatos de bário e cálcio para construção e caracterização de catodos termiônicos impregnados para aplicação em dispositivos de microondas de potência" / INVESTIGATION OF BARIUM-CALCIUM ALUMINATE PROCESS TO MANUFACTURE AND CHARACTERIZE IMPREGNATED THERMIONIC CATHODE FOR POWER MICROWAVE DEVICESHigashi, Cristiane 20 October 2006 (has links)
O presente trabalho descreve os processos de preparação do aluminato de bário e cálcio, material emissor de elétrons, empregados nos catodos do tipo impregnado para utilização em uma válvula de microondas do tipo TWT. Os catodos investigados constituem-se de uma pastilha de tungstênio porosa impregnada com aluminato de bário e cálcio com proporção molar 5:3:2. Para a síntese do aluminato, utilizaram-se três diferentes métodos: reação em estado sólido, precipitação e cristalização. A termogravimetria auxiliou na consolidação dos procedimentos de preparação dos aluminatos de modo a definir os parâmetros de pirólise/calcinação. Verificou-se que a técnica que apresentou melhores características de síntese foi o método da cristalização, pois esta apresentou uma menor temperatura de formação do aluminato (800ºC) em atmosfera oxidante (O2), quando comparada às técnicas de reação em estado sólido e de precipitação (temperatura de 1000ºC em atmosfera redutora H2). Utilizou-se o conceito da distribuição da função trabalho prática (PWFD) de Miram para a caracterização termiônica dos catodos impregnados. Empregando-se este método, foi possível traçar o perfil termiônico do catodo com aluminato de bário e cálcio. As curvas PWFD apresentaram a função trabalho média do catodo aluminato de, aproximadamente, 2,00 eV. / In the present work it is described the barium calcium aluminate manufacture processes employed to produce impregnated cathodes to be used in a traveling-wave tube (TWT). The cathodes were developed using a tungsten body impregnated with barium and calcium aluminate with a 5:3:2 proportion (molar). Three different processes were investigated to obtain this material: solid-state reaction, precipitation and crystallization. Thermal analysis, thermogravimetry specifically, supported to determine an adequate preparation procedure (taking into account temperature, time and pirolisys atmosphere). It was verified that the crystallization showed a better result when compared to those investigated (solid-state reaction and precipitation techniques formation temperature is about 1000ºC in hydrogen atmosphere), whereas it presented the lower formation temperature (800ºC) in oxidizing atmosphere (O2). It was used the practical work function distribution theory (PWFD) of Miram to characterize thermionic impregnated cathode. The PWFD curves were used to characterize the barium-calcium aluminate cathode. PWFD curves shown that the aluminate cathode work function is about 2,00 eV.
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