[pt] Ferritas do tipo espinélio têm atraído atenção devido a suas propriedades magnéticas com possibilidade de aplicações em dispositivos spintrônicos e de memória magnética, além de aplicações em catálise. Este trabalho tem como objetivo sintetizar o espinélio de alumínio e ferro (FeAl2O4) pelo método de síntese reação de combustão e avaliar suas características estruturais e morfológicas bem como suas propriedades magnéticas devido a sua ampla possibilidade de aplicações. A síntese deste material foi feita utilizando soluções concentradas dos nitratos metálicos hidratados de ferro e alumínio, variando o tipo e quantidade de combustível no intuito de verificar sua influência na microestrutura do produto. Os combustíveis utilizados neste trabalho foram ureia e ácido cítrico, ambos em quantidade estequiométrica, dita ideal, calculada a partir da teoria química dos propelentes, além de reações com quantidades acima e abaixo do ideal. Uma síntese apenas utilizando os nitratos metálicos, sem combustível, foi feita para comparação. O produto final das diferentes sínteses foram caracterizados em termos de estrutura e composição por meio de difração de raios X (DRX), Microscopia Eletrônica de Varredura (MEV) e Microscopia Eletrônica Transmissão (MET). As propriedades magnéticas foram obtidas por magnetometria de amostra vibrante e a identificação das fases de ferro por espectroscopia Mössbauer. As análises indicaram que a amostra sintetizada sem combustível corresponde a óxidos de ferro e de alumínio, majoritariamente amorfo, com formação de partículas nanométricas de hematita (Fe2O3) e um comportamento paramagnético. As caracterizações das amostras produzidas com ureia apresentam maior cristalinidade em relação a sintetizada sem combustível, com a amostra em quantidade estequiométrica de ureia, resultando em um produto monofásico identificado como o espinélio FeAl2O4, misto. Já as amostras com excesso e deficiência de ureia tiveram como produto, além da formação do espinélio desejado, a formação de outra fase identificada como magnetita (Fe3O4), sendo todas as amostras sintetizadas com ureia manifestando comportamento ferromagnético. As amostras sintetizadas com ácido cítrico, em todas as condições, apresentaram um sistema trifásico constituído pelo espinélio, magnetita e hematita e mostraram comportamento também ferromagnético. Neste trabalho é mostrado que a síntese por reação de combustão se mostrou eficiente para produzir o FeAl2O4, alcançando melhores resultados utilizando ureia como combustível, em quantidade ideal. / [en] Spinel-like ferrites has attracted attention due to its magnetic properties with the possibility of spintronic and magnetic memory devices applications as well as catalysis applications. This work aims to synthesize aluminum and iron spinel (FeAl2O4) by combustion reaction synthesis method and evaluate its structural and morphological characteristics, as well as its magnetic properties due to its wide application possibilities. The synthesis of this material was made using concentrated solutions of hydrated iron and aluminum metal nitrates, varying the type and quantity of fuel in order to verify its influence on the product microstructure. The fuels used in this work were urea and citric acid, both in stoichiometric quantity, said ideal, calculated from the chemical theory of propellants, and reactions with quantities above and below ideal. A synthesis using only metal nitrates without fuel was made for comparison. The final product of the different syntheses were characterized in terms of structure and composition by Xray diffraction (XRD), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). Magnetic properties were obtained by vibrating sample magnetometry and the iron phase identification by Mössbauer spectroscopy. The analysis indicated that the sample synthetized without fuel corresponds to iron and aluminum oxides, mostly amorphous, with formation of nanometer hematite particles (Fe2O3) and a paramagnetic behavior. The characterizations of the samples produced with urea show higher crystallinity than the synthesized without fuel, with the sample in stoichiometric amount of urea, resulting in a single phase product identified as FeAl2O4 mixed spinel. The samples with excess and deficiency of urea had as product, besides the formation of the desired spinel, the formation of another phase identified as magnetite (Fe3O4), being all the samples synthesized with urea manifesting ferromagnetic behavior. The samples synthesized with citric acid, under all conditions, presented a triphasic system consisting of spinel, magnetite and hematite and showed also ferromagnetic behavior. In this work it is shown that combustion reaction synthesis was efficient to produce FeAl2O4, achieving better results using urea as fuel, in ideal quantity.

De nouveaux alliages Zn-TR1-5 %mass.(TR = Ce, La et Mischmetal : Ce 75%/La25%) ont été synthétisés par fusion sous atmosphère contrôlée et coulés sous forme de plaques. Dans ces nouveaux matériaux, les terre rare sont localisées exclusivement dans des phases intermétalliques dispersées de manière homogène dans la matrice de zinc : Zn11Ce, Zn13La ou Zn11Ce1-xLax and Zn13CeyLa1-y. Le comportement électrochimique de ces nouveaux alliages a été étudié dans un milieu corrosif de référence simulant les conditions atmosphériques. En parallèle, les phases intermétalliques pures Zn11Ce and Zn13La ont été synthétisées et leur influence électrochimique a été évaluée par voltamétrie et couplage galvanique. Les résultats montrent que les deux phases intermétalliques sont des sites cathodiques préférentiels de la réduction du dioxygène et induisent une inhibition cathodique de la corrosion des alliages Zn-TR par rapport au zinc pur. Ce phénomène est plus marqué dans le cas des alliages au lanthane. Dans le cas spécifique des alliages au cérium, une inhibition anodique a également été observée et corrélée avec une modification chimique des produits de corrosion (composés majoritairement d'hydrozincite). En fait, une faible quantitéhomogène de cérium a pu être mise en évidence dans la couche de corrosion par spectrométrie dispersive en longueur d'onde. D'après les résultats d'expériences de précipitation contrôlée de sels de cérium et zinc en milieu carbonaté, la présence de cérium dans la couche de corrosion et son caractère protecteur pourraient être attribués à la formation d'un composé mixte double lamellaire zinc-cérium. L'addition de moins de 2%mass. de cérium ou lanthane permet d'améliorer la résistance à la corrosion du zinc. Cependant, lorsque la teneur en terre-rare augmente, l'effet de couplage galvanique devient plus important et rend les alliages moins résistants que le zinc pur / New Zn-RE1-5 wt.% alloys (RE=Ce, La and Mischmetal: Ce 75%/ La 25%) were synthesized by melting under controlled atmosphere and cast in plates. In these materials, rare earth metal are exclusively present in intermetallic phases homogeneously dispersed in the zinc matrix: Zn11Ce, Zn13La or Zn11Ce1-xLax and Zn13CeyLa1-y. The electrochemical behavior of these new alloys was investigated in a reference corrosivemedium. In parallel, the pure intermetallic phases Zn11Ce and Zn13La were synthesized and their electrochemical influence was studied by voltametry and galvanic coupling. Results show that both intermetallic phases act as preferential cathodic sites of dioxygen reduction and induce a cathodic inhibition of the corrosion of the Zn-RE alloys by comparison with pure zinc. This phenomenon is much more significant in the case of lanthanum containing alloys. In the specific case of cerium addition to zinc, an anodic inhibition was also observed and correlated with a chemical modification of the corrosion products (mainly made of hydrozincite). Actually, low quantities of cerium (less than 1 at.%) have been detected homogeneously in the corrosion layer by wave-length dispersive spectrometry. From results of controlled precipitation experiments of cerium and zinc salts performed in carbonated medium, the presence of cerium in the corrosionlayer and its protective character could be attributed to the formation of a mixed double lamellar zinc-cerium product. Therefore, addition to zinc of less than 2 wt.% of cerium or lanthanum allow to improve the corrosion resistance of zinc. However, by increasing the rare earth content in the alloys, the galvanic coupling phenomenon becomes more important and makes the alloys less resistant than pure zinc

O aumento no consumo energético mundial e a perspectiva de esgotamento das reservas de combustíveis fósseis têm estimulado o desenvolvimento de tecnologias e materiais para aplicações nos futuros reatores de fusão nuclear e reatores de fissão a nêutrons rápidos. O foco deste trabalho é avaliar a estabilidade microestrutural de um material tecnologicamente promissor por meio de diferentes técnicas de caracterização. O material estudado, o aço ODS-EUROFER, é um aço ferrítico-martensítico de atividade reduzida de composição 9%Cr-1%W (em massa) endurecido pela dispersão de 0,3% (em massa) de óxido de ítrio. Amostras foram laminadas até 80% de redução e submetidas a tratamentos isotérmicos em 800 °C por até 6 meses (4320 h) de duração para se investigar a ocorrência de fenômenos tais como recuperação, recristalização, crescimento de grão, precipitação e engrossamento de Ostwald. Outro conjunto de amostras foi recozido por 1 hora em temperaturas entre 900 e 1300 °C para se estudar a transformação martensítica neste material. Diversas técnicas de caracterização microestrutural complementares entre si (MEV, MET, DRX, EBSD, APT, ensaios de microdureza Vickers, dilatometria, DTA e magnetização) foram empregadas. Os resultados obtidos indicam que a dispersão de partículas nanométricas de Y2O3 confere uma grande resistência à recristalização primária, favorecendo a recuperação estática como principal mecanismo de amolecimento durante o recozimento prolongado deste aço. De modo similar, o crescimento de grão foi suprimido no campo austenítico em temperaturas tão altas quanto 1200 °C. / The rise in the world energy consumption and the possibility of depletion of the fossil fuel reserves have stimulated the development of new technologies and new materials for applications in the future nuclear fusion reactors and in the fast breeder fission reactors. The aim of this study is to evaluate the microstructural stability of a technologically promising material by using different characterization techniques. The investigated material, the ODS-EUROFER steel, is 9Cr-1W (%wt) reduced-activation ferritic-martensitic steel reinforced with a dispersion of 0.3%wt of yttrium oxide nanoparticles. Samples were cold rolled to 80% thickness reduction and subjected to isothermal annealing at 800 °C for up to 6 months (4,320 h) to investigate the occurrence of phenomena such as recovery, recrystallization, grain growth, precipitation, and Ostwald ripening. Another set of samples was annealed for 1 hour at temperatures between 900 and 1300 °C to study the martensitic transformation in this steel. Several complementary microstructural characterization techniques were employed (SEM, TEM, XRD, EBSD, APT, Vickers hardness, dilatometry, DTA and magnectic measurements). The results suggest that the dispersion of nanoscaled particles of Y2O3 provides a high resistance to discontinous recrystallization and favors static recovery as the main softening mechanism during long-term annealing in this steel. Similarly, grain growth was suppressed even in temperatures as high as 1200 °C in the austenitic field.

Made available in DSpace on 2017-07-21T20:43:46Z (GMT). No. of bitstreams: 1 Jean Cleber Bertoni.pdf: 7862049 bytes, checksum: 4c77f7ebc3fc211aac8ad8a7de58ccad (MD5) Previous issue date: 2015-01-30 / There are currently extensive research on aluminum alloys, mainly due to its wide application in the automotive and aerospace industries, due to the following characteristics, among them, low density, high thermal conductivity and high corrosion resistance at room temperature. Al-Fe alloys have a high degree of microstructural change due to changes in their properties when appropriate techniques are applied. The Al-Fe alloy was studied in the composition of 1.5% Fe by weight, which was subjected to the treatment laser surface remelting in order to enhance its surface characteristics. The characterization of these alloys in order to determine the variation of the chemical composition at different depths was performed by Grazzing incidence x-ray diffraction (GIXRD). In this technique, the angle of incidence of the X-ray beam was fixed and the detector moved in 2θ, it is possible to obtain the XRD patterns at different depths by varying the angle of incidence. In this work, the characterizations the micro and nano structural sample of alloy Al-1.5wt.%Fe treated by laser surface remelting (LSR) were performed, on the treated surface, as well as the transverse section, this study was performed at treated samples surface and at the isolated weld fillet on samples, where were applied laser beam speeds of 20, 40 and 60 mm / s. In this study we used different characterization techniques, such as, optical microscopy, scanning electron microscopy, energy dispersive spectroscopy, together with atomic force microscopy, and the Vickers hardness. Also in this work the technique of GIXRD was used to obtain depth profiles of near the surface chemical composition of the alloy. The analysis was performed in the micrometer range varying the angle of incidence between 0.5° to 6° in steps of 0.5° and analysis with incident angles 3° and 6° in steps of 0.02° for each 10 sec. As a result by examining the microstructure was characterized melted zone, the heat affected zone and the substrate, a particular features were found for each velocity of the laser beam, generally the treated area showed a more homogenous microstructure consisting of grains smaller feature, with low roughness and high hardness. The heat affected zone was more notorious the morphology of grains elongated feature in the treated and untreated interface for low laser beam scanning velocities. By means of the technique of X-ray diffraction various metastable phases were found, such as aluminum oxide, nitrides, etc., with different intensities of peaks as a consequence of the variation of angle of incidence. / Atualmente há uma ampla investigação sobre ligas de alumínio, principalmente devido a sua larga aplicação na indústria automotiva e aeroespacial, devido as seguintes características, entre elas, a baixa densidade, alta condutividade térmica e elevada resistência à corrosão a temperatura ambiente. Ligas de Al-Fe possuem um alto grau de modificação microestrutural, devido a mudanças em suas propriedades quando técnicas adequadas forem aplicadas. A liga Al-Fe foi estudada na composição de 1,5% de Fe em peso, a qual foi submetida ao tratamento de refusão superficial a laser de modo a aprimorar suas características superficiais. A caracterização dessas ligas com a finalidade de determinar à variação de composição química em diferentes profundidades foi realizado mediante a difração de raios X com ângulo de incidência rasante (DRXIR). Nesta técnica, o ângulo de incidência do feixe de raios X foi fixado e o detector moveu-se em 2θ, sendo possível obter os difratogramas em diferentes profundidades com a variação do ângulo de incidência. Neste trabalho, as caracterizações a nível micro e nano estrutural das amostras da liga Al-1,5%Fe tratadas por refusão superficial a laser (RSL) foram realizadas, tanto na superfície tratada e bem como na parte transversal, este estudo foi realizado nas amostras tratadas em toda a superfície, quanto nas amostras com trilhas isoladas que foram aplicadas as velocidades de feixe laser de 20, 40 e 60 mm/s. Para isso foram utilizados diferentes técnicas de caracterização, tais como, microscópio ótico, microscópio eletrônico de varredura, espectroscopia por energia dispersiva, acompanhada da microscopia de força atômica, bem como da microdureza Vickers. Também neste trabalho a técnica de DRXIR foi utilizada para obtenção de perfis de profundidade da composição química próxima à superfície da liga. A análise foi realizada em escala micrométrica por meio da variação do ângulo de incidência entre 0,5° a 6° com passos de 0,5°, bem como as análises com ângulos incidentes de 3º e 6º com passos de 0,02º a cada 10 s. Como resultado mediante o estudo microestrutural foram caracterizados a zona fundida, a zona afetada termicamente e o substrato, sendo encontradas características particulares para cada velocidade do feixe de laser, de modo geral a zona tratada mostrou ter uma característica microestrutural mais homogênea formada por grãos menores, com baixa rugosidade e de alta dureza. A zona afetada termicamente mostrou ser mais notória a morfologia de grãos com característica alongada na interface tratada e não tratada para baixas velocidades de varredura do feixe laser. Por meio da técnica de difração de raios X diferentes fases metaestáveis foram encontradas, tais como, óxido de alumínio, nitretos, etc, com diferentes intensidades de picos como consequência da variação do ângulo de incidência.

Materiais odontológicos inovadores que apresentem propriedades antimicrobianas são altamente desejáveis na cavidade oral. O objetivo deste estudo foi avaliar a atividade antimicrobiana do vanadato de prata nanoestruturado (&beta;-AgVO3) incorporado em duas resinas acrílicas frente a Candida albicans, Streptococcus mutans, Staphylococcus aureus e Pseudomonas aeruginosa, além de examinar as propriedades mecânicas e o padrão de incorporação do nanomaterial nas resinas. O nanomaterial foi caracterizado por difração de raios X (DRX), espectroscopia no infravermelho por transformada de Fourier (FTIV), análise elementar por energia dispersiva (EDS) e microscopia eletrônica de varredura (MEV). As propriedades antimicrobianas das resinas acrílicas incorporadas com diferentes porcentagens de &beta;-AgVO3 foram investigadas pelo método de redução do XTT, unidades formadoras de colônias (UFC) e microscopia confocal à laser e o comportamento mecânico por meio de ensaios de dureza e rugosidade superficial, resistência à flexão, à compressão e ao impacto. O padrão de incorporação do &beta;-AgVO3 nas resinas foi analisado por microscopia eletrônica de varredura (MEV) e análise elementar por energia dispersiva (EDS). Os dados foram analisados por ANOVA, Tukey e pelo teste Generalized Linear Models (&alpha;=0,05). Para ambas as resinas, em relação ao grupo controle, a incorporação de 5% e 10% de &beta;-AgVO3 reduziram significantemente a atividade metabólica de C. albicans e P. aeruginosa (p<0,05), enquanto que para S. mutans houve redução significante apenas com a incorporação de 10% (p<0,05). Não houve diferença na atividade metabólica pelo método do XTT frente a S. aureus (p> 0,05). Para ambas as resinas, observou-se uma redução significativa no número de UFC/mL de C. albicans para o grupo incorporado com 10% de &beta;-AgVO3 e de S. mutans para os grupos com 2,5%, 5% e 10% do nanomaterial (p<0,05). Para S. aureus e P. aeruginosa, houve redução significante com a incorporação de 5% e 10% (p<0,05). A dureza superficial da resina termopolimerizável permaneceu inalterada pela incorporação do nanomaterial (p>0,05) e da autopolimerizável aumentou com 0,5% (p<0,05). Concentrações maiores que 1% promoveram redução na resistência flexural das resinas (p<0,05) enquanto que a rugosidade superficial permaneceu inalterada (p>0,05). A resistência à compressão da resina autopolimerizável permaneceu inalterada (p>0,05) e da termopolimerizável reduziu com a incorporação de 0,5% e 10% (p<0,05). As concentrações de 5% e 10% promoveram redução significante na resistência ao impacto das resinas, em relação ao controle (p<0,05). A caracterização das resinas quanto a dispersão da carga utilizada mostrou a presença de domínios de &beta;-AgVO3 ao longo da matriz polimérica seguindo um padrão circular. Conclui-se que o método proposto foi capaz de promover atividade antimicrobiana às resinas acrílicas frente aos micro-organismos avaliados, sendo a mesma dependente da concentração do nanomaterial. Porém, alterações na dispersão do &beta;-AgVO3 na matriz dos polímeros são necessárias para não sacrificar as propriedades mecânicas e para potencializar o efeito antimicrobiano / Innovative dental materials that have antimicrobial properties are highly desirable in the oral cavity. The aim of this study was to evaluate the antimicrobial activity of nanostructured silver vanadate (&beta;-AgVO3) incorporated into two acrylic resins against Candida albicans, Streptococcus mutans, Staphylococcus aureus and Pseudomonas aeruginosa, while examining the mechanical properties and the pattern of nanomaterial incorporation into resins. The nanomaterial was characterized by X-ray diffraction (XRD), infrared spectroscopy Fourier transform (FTIR), elemental analysis by energy dispersive (EDS) and scanning electron microscopy (SEM). The antimicrobial properties of acrylic resins incorporated with different percentages of &beta;-AgVO3 were investigated by the reduction of XTT method, colony forming units (CFU) and confocal laser microscopy and the mechanical behavior through hardness, surface roughness, flexural, compression and impact tests. The pattern of incorporation of &beta;-AgVO3 resins was analyzed by scanning electron microscopy (SEM) and elemental analysis by energy dispersive (EDS). Data were analyzed by ANOVA, Tukey test and the Generalized Linear Models (&alpha; = 0.05). For both resins, compared to the control group, the incorporation of 5% and 10% &beta;-AgVO3 caused a significantly reduced in the metabolic activity of C. albicans and P. aeruginosa (p <0.05), while for S. mutans significant reduction was observed only with the incorporation of 10% (p <0.05). There was no difference in metabolic activity by XTT method against S. aureus (p> 0.05). For both resins, there was a significant reduction in the number of CFU / mL for C. albicans incorporated group with 10% &beta;-AgVO3 and S. mutans in groups with 2.5%, 5% and 10% of nanomaterial (p <0.05). For P. aeruginosa and S. aureus, there was a significant decrease with the incorporation of 5% to 10% (p <0.05). The surface hardness of the heat-cured resin was unchanged by the incorporation of the nanomaterial (p <0.05) and increased self-cured with 0.5% (p <0.05). Concentrations above 1% promote the reduction in flexural strength of the resins (p <0.05) while the surface roughness remained unchanged (P> 0.05). The compressive strength of the self-cured resin remained unchanged (P> 0.05) and heat-cured reduced with the incorporation of 0.5% and 10% (p <0.05). Concentrations of 5% and 10% caused a significant reduction in impact strength of resins, compared to control (p <0.05). The characterization of the resins as the dispersion of the filler used showed the presence of &beta;-AgVO3 domains along the polymer matrix following a circular pattern. It was concluded that the proposed method was able to promote antimicrobial activity to acrylic resins against microorganisms evaluated, with the same concentration dependent of the nanomaterial. However, changes in the &beta;-AgVO3 dispersion in the polymer matrix are necessary to do not sacrifice the mechanical properties and to enhance the antimicrobial effect

La rentabilité des cellules à base de silicium est un point essentiel pour le marché photovoltaïque et cela passe notamment par l'amélioration du rendement électrique, la baisse des coûts de production ainsi que le renforcement de la fiabilité/durabilité des wafers. Des procédés innovants émergent, qui permettent d'obtenir des wafers ultra minces avec moins de perte de matière première. Cependant il est nécessaire de mettre en place des méthodes de caractérisation afin d’analyser la rigidité et la tenue mécanique de ces matériaux. Dans ce travail, des essais de flexion ont été effectués pour caractériser à la fois la rigidité et la rupture. Afin d’étudier la rupture fragile, une caméra rapide a été utilisée, des analyses fractographiques ont été menées. La diffraction d'électrons rétrodiffusés et la diffraction par rayon X de Laue ont été utilisées afin d'explorer le lien entre les orientations cristallographiques et les comportements observés. Conjointement, des simulations numériques EF ont été mise en place. Grâce à ce couplage expériences-simulations numériques, une caractérisation fiable de la rigidité des wafers a été effectuée. Une stratégie d'identification de l'origine de la rupture est également proposée. L'étude de la rupture du silicium monocristallin a mis en évidence la stabilité du clivage (110), la grande vitesse d'amorçage de la fissure, la dépendance de la forme du front de fissure à la vitesse de propagation ainsi que l'apparition de "Front Waves" pour les fissures à très grande vitesse. L'étude de la rupture des wafers multi-cristallins démontre une fissuration intra-granulaire. Des éprouvettes jumelles ont permis d’étudier la répétabilité du chemin de fissuration : une attention particulière a été portée à la nature des plans de clivage ainsi que l'effet des joints de grains. Enfin, une modélisation par la méthode des éléments finis étendus est proposée. Elle permet de reproduire le chemin de fissuration expérimentalement observé. / The profitability of silicon solar cells is a critical point for the PV market and it requires improved electrical performance, lower wafer production costs and enhancing reliability and durability of the cells. Innovative processes are emerging that provide thinner wafers with less raw material loss. But the induced crystallinity and distribution of defects compared to the classical wafers are unclear. It is therefore necessary to develop methods of microstructural and mechanical characterization to assess the rigidity and mechanical strength of these materials. In this work, 4-point bending tests were performed under quasi-static loading. This allowed to conduct both the stiffness estimation and the rupture study. A high speed camera was set up in order to track the fracture process thanks to a 45° tilted mirror. Fractographic analysis were performed using confocal optical microscope, scanning electron microscope and atomic force microscope. Electron Back-Scatter Diffraction and Laue X-Ray diffraction were used to explore the relationship between the microstructural grains orientations/textures of our material and the observed mechanical behavior. Jointly, finite element modeling and simulations were carried out to provide auxiliary characterization tools and help to understand the involved fracture mechanism. Thanks to the experiment-simulation coupled method, we have assessed accurately the rigidity of silicon wafers stemming from different manufacturing processes. A fracture origin identification strategy has been proposed combining high speed imaging and post-mortem fractography. Fracture investigations on silicon single crystals have highlighted the deflection free (110) cleavage path, the high initial crack velocity, the velocity dependent crack front shape and the onset of front waves in high velocity crack propagation. The investigations on the fracture of multi-crystalline wafers demonstrate a systematic transgranular cracking. Furthermore, thanks to twin multi-crystalline silicon plates, we have addressed the crack path reproducibility. A special attention has been paid to the nature of the cleavage planes and the grain boundaries barrier effect. Finally, based on these observations, an extended finite element model (XFEM) has been carried out which fairly reproduces the experimental crack path.

O aumento no consumo energético mundial e a perspectiva de esgotamento das reservas de combustíveis fósseis têm estimulado o desenvolvimento de tecnologias e materiais para aplicações nos futuros reatores de fusão nuclear e reatores de fissão a nêutrons rápidos. O foco deste trabalho é avaliar a estabilidade microestrutural de um material tecnologicamente promissor por meio de diferentes técnicas de caracterização. O material estudado, o aço ODS-EUROFER, é um aço ferrítico-martensítico de atividade reduzida de composição 9%Cr-1%W (em massa) endurecido pela dispersão de 0,3% (em massa) de óxido de ítrio. Amostras foram laminadas até 80% de redução e submetidas a tratamentos isotérmicos em 800 °C por até 6 meses (4320 h) de duração para se investigar a ocorrência de fenômenos tais como recuperação, recristalização, crescimento de grão, precipitação e engrossamento de Ostwald. Outro conjunto de amostras foi recozido por 1 hora em temperaturas entre 900 e 1300 °C para se estudar a transformação martensítica neste material. Diversas técnicas de caracterização microestrutural complementares entre si (MEV, MET, DRX, EBSD, APT, ensaios de microdureza Vickers, dilatometria, DTA e magnetização) foram empregadas. Os resultados obtidos indicam que a dispersão de partículas nanométricas de Y2O3 confere uma grande resistência à recristalização primária, favorecendo a recuperação estática como principal mecanismo de amolecimento durante o recozimento prolongado deste aço. De modo similar, o crescimento de grão foi suprimido no campo austenítico em temperaturas tão altas quanto 1200 °C. / The rise in the world energy consumption and the possibility of depletion of the fossil fuel reserves have stimulated the development of new technologies and new materials for applications in the future nuclear fusion reactors and in the fast breeder fission reactors. The aim of this study is to evaluate the microstructural stability of a technologically promising material by using different characterization techniques. The investigated material, the ODS-EUROFER steel, is 9Cr-1W (%wt) reduced-activation ferritic-martensitic steel reinforced with a dispersion of 0.3%wt of yttrium oxide nanoparticles. Samples were cold rolled to 80% thickness reduction and subjected to isothermal annealing at 800 °C for up to 6 months (4,320 h) to investigate the occurrence of phenomena such as recovery, recrystallization, grain growth, precipitation, and Ostwald ripening. Another set of samples was annealed for 1 hour at temperatures between 900 and 1300 °C to study the martensitic transformation in this steel. Several complementary microstructural characterization techniques were employed (SEM, TEM, XRD, EBSD, APT, Vickers hardness, dilatometry, DTA and magnectic measurements). The results suggest that the dispersion of nanoscaled particles of Y2O3 provides a high resistance to discontinous recrystallization and favors static recovery as the main softening mechanism during long-term annealing in this steel. Similarly, grain growth was suppressed even in temperatures as high as 1200 °C in the austenitic field.

Friction Stir Processing (FSP) is a promising thermomechanical technique that is used to modify the microstructure of metals locally, and thereby locally improve mechanical properties of the material. FSP uses a simple and inexpensive tool, and has been shown to eliminate pores and also reduce the sizes of intermetallics in aluminum alloys. This is of great interest for research on solidification, production and performance of aluminum alloy castings because FSP can enhance the structural quality of aluminum casting significantly by minimizing the effect of those structural defects. In the literature, there is evidence that the effectiveness of FSP can change with tool wear of the tool used. Therefore, a study was first conducted to determine the effect of FSP time on the tool life and wear in 6061-T6 extrusions. Results showed the presence of two distinct phases in the tool life and wear. Metallographic analyses confirmed that wear in Phase I was due to fracture of the threads of the tool and Phase II was due to regular wear, mostly without fracture. Moreover, built-up layers of aluminum were observed between threads. The microhardness profile was found to be different from those reported in the literature for 6061-T6, with Vickers hardness increasing continuously from the the stir zone to the base material. To investigate the degree of effectiveness of FSP in improving the structural quality of cast A356 alloys, ingots with different quality (high and low) were friction strir processed with single and multiple passes. Analysis of tensile test results and work hardening characteristics showed that for the high quality ingot, a single pass was sufficient to eliminate the structural defects. Subsequent FSP passes had no effect on the work hardening characteristics. In contrast, tensile results and work hardening characteristics improved with every pass for the low quality ingot, indicating that the effectiveness of FSP was dependent on the initial quality of the metal. The evolution of microstructure, specifically the size and spacing of Silicon (Si) eutectic particles, was investigated after friction stir processing of high quality A356 castings with single and multiple passes. Si particles were found to coarsen with each pass, which was in contrast with previous findings in the literature. The nearest neighbor distance of Si particles also increased with each FSP pass, indicating that microstructure became progressively more homogeneous after each pass. In the literature, the improvement observed after FSP of Al-Si cast alloys was attributed to the refinement of Si particles. Tensile data from high quality A356 ingot showed that there was no correlation between the size of Si particles and ductility. To the author’s knowledge, this is the first time that the absence of a correlation between Si particle size and ductility has been found.

Cette thèse porte sur la fonctionnalisation de fils en acier inoxydable via des revêtements colorés base titane, élaborés par pulvérisation cathodique avec un magnétron cylindrique. Ce travail s’intéresse à la caractérisation chimique, morpho-structurale et à l’évaluation de la durabilité mécano-chimique des fils revêtus.Premièrement, la vitesse de dépôt et la composition chimique des films sont déterminées dans des conditions statiques. Les hétérogénéités du plasma dans la cathode sont démontrées et reliées aux paramètres tels que la puissance, la pression et la polarisation d’anodes auxiliaires.Les dépôts monocouches de Ti, TiN et TiOx sont ensuite élaborés en continu. La relation entre la couleur du TiN et sa composition chimique est établie. La couleur dorée est obtenue pour des films stœchiométriques contenant peu d’oxygène (< 5 %at.). Les microstructures sont caractérisées par MET-ASTAR et des cartographies d’orientation sont dressées à l’échelle nanométrique. Tandis que les dépôts de TiN sont colonnaires avec une texturation selon <111>, les grains des films de Ti sont plutôt équiaxes et orientés selon <0001>. Pour une température d’élaboration de 650 °C, les éléments du substrat diffusent dans les films et mènent à la formation de phases de Laves. Les dépôts de TiOx, élaborés en mode métallique, présentent des couleurs d’interférence et une composition proche du monoxyde. Les surfaces revêtues de TiN ont une résistance à la corrosion élevée semblable à l’acier inoxydable 316L, contrairement aux fils revêtus de Ti et TiOx. La ténacité et l’énergie d’adhérence des revêtements sont déterminées par traction in-situ sous MEB : Ti et TiN sont particulièrement adhérents au substrat contrairement à TiOx.Enfin, les dépôts sont architecturés avec l’ajout d’un dépôt de titane entre le substrat et le revêtement céramique. Ainsi, l’adhérence du film Ti-TiOx est largement augmentée par rapport au monocouche TiOx (5 à 200 J/m2). Enfin, les études microstructurales et électrochimiques montrent qu’un paramètre clef de la résistance à la corrosion est la présence de porosité ouverte dans les revêtements. / This thesis treats of the functionalization of stainless steel wires with colored Ti-based coatings, grown by PVD with a cylindrical magnetron, their chemical and morpho-structural characterization, and the evaluation of the chemico-mechanical durability of the coated wires.First, the deposition rate and the chemical composition of the films are determined under static conditions. Cathode plasma heterogeneities are demonstrated and related to parameters such as power, pressure and polarization of auxiliary anodes.Then, Ti, TiN and TiOx monolayer coatings are grown continuously. The relationship between the color of TiN and its chemical composition is established and golden color is obtained for stoichiometric films with low oxygen content (<5% at.). Microstructures are studied with TEM-ASTAR and orientation maps are obtained with a nanometric resolution. While TiN coatings are columnar with <111> texture, Ti grains are rather equiaxed and <0001> oriented. With a 650 ° C substrate temperature, substrate elements diffuse into the films which results in Laves phase formation. TiOx is grown in metallic mode, presents interference colors and a composition close to monoxide. TiN coated surfaces display high corrosion resistance similar to 316L stainless steel, unlike Ti and TiOx coated wires. The toughness and the adhesion energy of the coatings are determined by SEM in-situ tensile tests: Ti and TiN are particularly adherent to the substrate in contrast to TiOx.Finally, coatings are architectured with the addition of a titanium interlayer between the substrate and the ceramic coating. Thus, Ti-TiOx film adhesion is greatly superior compared to the TiOx monolayer (5 to 200 J/m2). Finally, microstructural and electrochemical studies show that a key parameter of corrosion resistance is the presence of open porosity in the coatings.

Made available in DSpace on 2016-12-08T17:19:23Z (GMT). No. of bitstreams: 1 Andrea Luciane M Soares.pdf: 1356785 bytes, checksum: 08654c7f08e5db11d8746af3551cd3ed (MD5) Previous issue date: 2014-07-28 / Coordenação de Aperfeiçoamento de Pessoal de Nível Superior / This work investigates the effect by partial replacement of nanosilica (nS) of Portland cement on the mechanical, physical, chemical and microstructural Portland cement mortar properties. For better understanding of the effects and a more detailed analysis of the results, the 33-1 fractional factorial design to design of experiments was used with three factors, each at three levels: nS content cement replacement (1, 2 and 3wt. %), water/cement ratio (1.1, 1.4 and 1.7 weight) and the aggregate/cement ratio (7.04 factor, 8.53 and 10.05 weight). The processing of the nine mortar mixtures was performed according to standards of the manufacture of such construction materials (composition, mixing, molding, curing and specimen preparation). Mechanical properties were evaluated in the fresh state (flow table) and in the hardened state (compressive strength at 7, 28 and 90 days of curing). In order to correlate the compressive strength with the microstructural characteristics, physic, chemical and microstructural characterization was performed. X-ray diffraction (XRD), infrared spectroscopy (FTIR), thermal (TG/DTA) and scanning electron microscopic with energy-dispersive X-ray spectrometry (SEM/EDS) analyses were used on selected samples. The use of fractional factorial design and the response surface methodology was found to be in the design the experimental and statistical analyses. The addition of nS affects the mechanical properties of mortars, both in the fresh, and in the hardened state. Materials with adequate workability for use in construction industry (consistency of 230 ± 10 mm) and high compressive strength after 7 (&#8805; 3 MPa) and 28 days of curing (&#8805; 6 MPa) were obtained with the following composition: 1.5 wt. % nS, 1.3 water/cement ratio and aggregate/cement ratio kept constant of 10.1. The physical-chemical and microstructural characterization showed that nS contributes to improve the packing of the amorphous calcium silicate hydrate (C-S-H) and crystalline phases matrix and aggregate. Moreover, nS participates in the hydration reactions of Portland cement due to its reaction with calcium hydroxide. Thus, a more cohesive matrix and less calcium hydroxide contributes to lower porosity, thus reducing permeability, which contributes for better durability of the mortars containing nS. / Este trabalho investiga o efeito da substituição parcial de cimento Portland por nanosílica (nS) nas propriedades mecânicas, físico-químicas e microestruturais de argamassas de cimento Portland. Para melhor compreensão dos efeitos e uma análise mais detalhada dos resultados, foi usado o planejamento fatorial fracionado 33-1 para projeto dos experimentos. No projeto foram utilizados três fatores, cada qual em três níveis: o teor de nS em substituição ao cimento (1%, 2% e 3% em massa), a proporção de água/cimento (1,1; 1,4 e 1,7 em massa) e o fator agregado/cimento (7,04; 8,53 e 10,05 em massa). O processamento das nove misturas de argamassas foi realizado de acordo com as normas de fabricação desses materiais de construção civil (pesagem, mistura, moldagem, cura e preparação de corpos de prova). Propriedades mecânicas foram avaliadas no estado fresco (índice de consistência) e no estado endurecido (resistência mecânica à compressão em 7, 28 e 90 dias de cura). Com o objetivo de correlacionar a resistência à compressão com as características microestruturais, foi realizada a caracterização físico-química e microestrutural, por meio de análises de raios X (DRX), espectroscopia de infravermelho por transformada de Fourier (FTIR), análises térmicas (TG) e análise térmica diferencial (ATD) e de microscopia eletrônica de varredura (MEV/EDS) em amostras selecionadas. O uso do projeto fatorial fracionado se mostrou eficiente para o planejamento experimental e análises estatísticas juntamente com o uso da metodologia de superfície de resposta. A adição de nS nas argamassas afeta as propriedades mecânicas das argamassas, tanto no estado fresco, como no endurecido. Materiais com trabalhabilidade adequada para uso na construção civil (índice de consistência de 230 ± 10 mm) e elevada resistência à compressão após 7 (&#8805; 3MPa) e 28 dias de cura (&#8805; 6 MPa) foram obtidas com as seguintes composições: 1,5% de nS, 1,3 água/cimento e 10,1 agregado/cimento. A caracterização físico-química e microestrutural mostrou que a nS contribui para melhorar o empacotamento da matriz formada pelo silicato de cálcio hidratado amorfo (C-S-H), fases cristalinas e os agregados. Além disso, a nS participa das reações de hidratação do cimento Portland, por meio do consumo de hidróxido de cálcio. Dessa forma, uma matriz mais coesa e menos hidróxido de cálcio contribui para uma menor porosidade, reduzindo a permeabilidade, que se traduz numa melhor durabilidade das argamassas contendo nS.