Os bisfosfonatos representam uma classe de drogas que agem sobre o metabolismo ósseo e são amplamente utilizadas na prevenção e tratamento de estados osteopênicos e osteoporóticos. Os objetivos do presente estudo foram avaliar, in vivo, o efeito do uso sistêmico de alendronato sódico: na densidade mineral óssea de ratos, por meio da densitometria óptica radiográfica e da técnica de absortometria radiológica de dupla energia (DXA); e nas estruturas dentárias mineralizadas de incisivos murinos, por meio da espectrometria na região do infravermelho, espectroscopia de fluorescência, microdureza transversal, microscopia eletrônica de varredura e microscopia de luz polarizada. Foram utilizados 45 ratos Wistar, com 36-42 dias de idade, pesando em média 200-230g, os quais foram divididos em dois grupos: experimental (n= 25) e controle (n= 20). No grupo experimental foram administradas duas doses semanais de 1mg/Kg de alendronato de sódio quimicamente puro diluído em água destilada, via gavagem, enquanto que os animais do grupo controle receberam apenas água destilada. Decorrido o período de 60 dias, os animais foram mortos por sobredose anestésica e, em seguida, foram extraídos os incisivos superiores e removidas as tíbias. As tíbias foram submetidas à avaliação da densidade mineral óssea por meio de análise radiográfica e da técnica de absortometria radiológica de dupla energia (DXA). Os incisivos superiores foram submetidos às seguintes avaliações: análise química por espectrometria na região do infravermelho e espectroscopia de fluorescência, microdureza transversal do esmalte e da dentina; microscopia eletrônica de varredura e microscopia de luz polarizada. Os resultados numéricos obtidos foram submetidos à análise estatística por meio do teste não-paramétrico de Kruskal-Wallis, utilizando o software SAS (Statistical Analysis System) for Windows versão 9.1.3. O nível de significância adotado foi de 5%. O grupo experimental apresentou valores de densidade mineral óssea superiores (p<0,05) em relação ao grupo controle, pelos métodos da densitometria óptica radiográfica e DXA. A análise química pelos métodos de espectrometria na região do infravermelho e espectroscopia de fluorescência permitiu detectar a presença do alendronato na estrutura dentária mineralizada do grupo experimental e que a porcentagem dessa incorporação foi de 0,0018% por elemento dental. Os resultados da microdureza transversal do esmalte e da dentina não revelaram diferença estatisticamente significante entre os grupos experimental e controle (p>0,05). Não foram observadas diferenças morfológicas significativas entre as amostras de ambos os grupos por meio da análise por microscopia eletrônica de varredura e microscopia de luz polarizada. Com base nos resultados obtidos, conclui-se que o tratamento com alendronato sódico provocou aumento na densidade mineral óssea da metáfise proximal da tíbia e que o alendronato incorporou-se nas estruturas dentárias mineralizadas, porém sem provocar efeitos significativos na microdureza e na morfologia do esmalte e da dentina de incisivos de ratos. / Bisphosphonates represent a class of drugs that act on bone metabolism and are widely used in the prevention and treatment of osteopenic and osteoporotic states. The objectives of this study were to evaluate, in vivo, the effect of the systemic use of sodium alendronate on: the mineral bone density of rats, by radiographic optical densitometry and dual-energy x-ray absorptiometry (DXA); the mineralized dental structures of murine incisors, by analysis of infrared (IR) spectrometry, fluorescence spectroscopy, cross-sectional microhardness (CSMH), scanning electron microscopy (SEM) and polarized light microscopy (PLM). Forty-five Wistar rats aged 36-42 days and weighing 200-230 g were assigned to two groups: experimental (n= 25) and control (n= 20). The experimental group received two weekly doses of 1 mg/kg of chemically pure sodium alendronate diluted in distilled water, via gavage, while the animals of the control group received only distilled water. After 60 days, the animals were killed by anesthetic overdose, and the maxillary incisors were extracted and the tibias were removed. The mineral bone density of the tibias was analyzed radiographically and by DXA. The maxillary incisors were subjected to the following evaluations: chemical analysis by IR spectrometry and fluorescence spectroscopy, enamel and dentin CSMH, SEM and PLM. The results were subjected to statistical analysis by the Kruskal-Wallis non-parametric test, using the SAS (Statistical Analysis System) software for Windows version 9.1.3. The significance level was set at 5%. The experimental group presented higher mineral bone density (p<0.05) than the control group, by radiographic optical densitometry and DXA. The chemical analysis by IR spectrometry and fluorescence spectroscopy revealed the presence of alendronate in the mineralized dental structure of the specimens of the experimental group, with a percentage of incorporation of 0.0018% per tooth. The results of enamel and dentin CSMH did not show statistically significant difference between the experimental and control groups (p>0.05). There were no significant morphological differences among the specimens of the groups by SEM and PLM. Based on the obtained results, it may be concluded that the treatment with sodium alendronate caused an increase in the mineral bone density of the proximal tibial metaphysis, and that alendronate was incorporated in the mineralized dental structures without causing significant effects in the enamel and dentin microhardness and morphology of rat incisors.

A qualidade óssea em grandes animais é avaliada pela densidade mineral óssea (DMO) utilizando a técnica de densitometria óptica em imagens radiográficas; o objetivo desse trabalho foi avaliar e comparar a qualidade óssea baseada na microarquitetura de uma forma inédita. Foram selecionados 20 bovinos, 10 da raça Canchim e 10 da raça Nelore, com controle dos processos biológicos e bioquímicos do nascimento até o abate aos 24 meses de idade, antes de entrarem na fase adulta. O osso metatarsal foi escolhido por suportar maior carga e amostras da diáfise do osso cortical seco foram obtidas. A avaliação da estrutura cristalina de ossos metatarsais secos foi realizada utilizando difração de raios X com a aplicação do método de refinamento de Rietveld, avaliando parâmetros de rede, tamanho de cristalito e microdeformação. A técnica de nanoindentação permitiu avaliar os módulos de elasticidade e valores de nanoindentação. A composição química razão cálcio e fósforo do material, resistência à deformação plástica, valores de microdureza, e imagens de microscopia eletrônica de varredura e microscopia óptica foram realizadas. A comparação entre os resultados das duas raças, Canchim e Nelore, dos valores de parâmetros de rede da estrutura cristalina da hidroxiapatita, tamanho de cristalito, microdeformações, relação cálcio e fósforo, microdurezas Vickers/Knoop, nanodureza Vickers e módulo de elasticidade indicaram que a qualidade óssea das raças Canchim e Nelore é estatisticamente semelhante para 30% dos parâmetros estudados e que para os demais 70% dos parâmetros estudados não há semelhança. / The bone quality in large animals is evaluated by bone mineral density (BMD) using the optical densitometry technique in radiographic images; The objective of this study was to evaluate and compare bone quality based on microarchitecture unpublished. Twenty bovines were selected, 10 from the Canchim breed and 10 from the Nelore breed, with control of the biological and biochemical processes from birth to slaughter at 24 months of age, before entering adulthood. The metatarsal bone was chosen because it supported higher load and samples of the diaphysis of the dry cortical bone were obtained. The evaluation of the crystalline structure of dry metatarsal bones was performed using X - ray diffraction with the application of the Rietveld refinement method, evaluating network parameters, crystallite size and microdeformation. The nanoindentation technique allowed to evaluate the modulus of elasticity and nanoindentation values. The chemical composition calcium and phosphorus ratio of the material, resistance to plastic deformation, values of microhardness, and scanning electron microscopy images and optical microscopy were performed. The comparison between the results of the two races, Canchim and Nelore, of the network parameter values of the hydroxyapatite crystal structure, crystallite size, microdeformations, calcium and phosphorus ratio, Vickers/Knoop microhardness, Vickers nanodness and modulus of elasticity indicated that Quality of the Canchim and Nelore races is statistically similar for 30% of the studied parameters and that for the ofter 70% of the studied parameters there is no similarity.

O presente estudo in vitro analisou o efeito de 3 sucos de fruta com baixo pH (suco de cupuaçu, taperebá e laranja), e saliva artificial (controle) sobre materiais restauradores indicados em lesões cervicais não cariosas: resina composta nanoparticulada (Filtek Z350 XT), cimento de ionômero de vidro resino modificado (Vitremer) e um cimento de ionômero de vidro convencional (Fuji II). Os materiais foram avaliados, quantitativamente, quanto à alteração de: peso, rugosidade superficial e microdureza superficial, e qualitativamente, por microscopia eletrônica de varredura (MEV). Foram confeccionados 144 corpos de prova para cada teste quantitativo (n=12) e 45 para o MEV (n=3), de (8mm de diâmetro x 2mm de altura). Os corpos de prova foram preparados, mantidos em saliva artificial por 24 h à 37º C, receberam acabamento em politriz, e em seguida foram realizadas as leituras iniciais. Durante um período de 10 dias consecutivos, os corpos de prova foram submetidos ao desafio erosivo (nos respectivos sucos de frutas) durante 30 minutos três vezes ao dia, totalizando 90 minutos/dia e mantidos em saliva artificial entre os intervalos. Após o período de ciclagem erosiva, foram realizadas as leituras finais. Os resultados obtidos foram submetidos ao teste t, ANOVA e Tukey. As médias de alteração entre os valores de peso finais e iniciais demonstraram diferença significativa (p<0,01) nos materiais estudados e em todos os sucos estudados, com exceção do Vitremer quando imerso no suco de taperebá (p>0,01). As médias de alteração entre os valores de rugosidade superficial final e inicial demonstraram diferença significativa (p<0,01) para todos os materiais estudados em todos os sucos, exceto a Filtek Z350 XT no grupo controle que não apresentou diferença significativa (p>0,01). A comparação entre os valores de microdureza final e inicial demonstrou diferença significativa (p<0,01) na microdureza dos materiais estudados em todos os meios de imersão, inclusive no grupo controle. De um modo geral o suco de taperebá foi o que provocou a maior alteração na superfície dos materiais restauradores quanto ao peso, rugosidade, microdureza e na microscopia eletrônica de varredura. A resina composta Filtek Z350 XT foi o material restaurador que menos sofreu alterações de superfície. Concluiu-se que os sucos das frutas estudados são capazes de alterar os materiais restauradores, sendo que a resina composta foi o material que sofreu menor alteração. / This in vitro study examined the effects of 3 fruit juices with low pH (cupuaçu, taperebá and orange) and artificial saliva (control) upon restorative materials indicated in noncarious cervical lesions: nanoparticle composite resin (Filtek Z350 XT), resin-modified glass ionomer cement (Vitremer) and a glass ionomer cement (Fuji II). The materials were evaluated quantitatively as for alterations in weight, surface roughness and surface microhardness, and qualitatively by scanning electronic microscopy (SEM). 144 specimens were prepared for each quantitative test (n = 12) and 45 for the SEM (n = 3), of (8mm diameter x 2mm height). The specimens were prepared, stored in artificial saliva for 24 hours at 37º C, were finished in a polishing machine, and then the initial readings were performed. During a period of 10 consecutive days, the specimens were subjected to erosive challenge (in the respective juices) for 30 minutes, three times a day, and totaling 90 minutes/day and kept in artificial saliva between intervals. After the erosive cycling period, the final readings were taken. The data were analyzed using t test, ANOVA and Tukey.Test The average alterations between the values of initial and final weight showed significant difference (p < 0.01) in the material studied and all the juices studied, except for Vitremer when immersed in taperebá juice (p > 0.01). The average alterations between the values of initial and final surface roughness showed a significant difference (p < 0.01) for all materials studied in all juices, except for Filtek Z350 XT, in the control group, that showed no significant differences (p > 0.01). The comparison between the values of initial and final microhardness showed a significant difference (p < 0.01) in microhardness of the materials studied in all immersion means, including the control group. In general, taperebá juice was the one that caused the biggest alterations in the surface of restorative materials with respect to weight, roughness, hardness and scanning electronic microscopy. The composite resin Filtek Z350 XT was the restorative material that suffered less surface alterations. It was concluded that the fruit juices studied are capable of altering the restorative materials, and composite resin was the material that has undergone minor changes.

O objetivo do presente trabalho foi avaliar diferentes tratamentos na remineralização do esmalte desmineralizado em situação de alto desafio cariogênico. Foram utilizados 55 fragmentos de esmalte bovino (4mmX4mmX2mm) planificados e polidos. Os espécimes foram cobertos com resina composta ficando exposta apenas a metade da superfície externa (2mmX4mm) e então, foram imersos em solução tampão de acetato (pH 4,7) por 43 horas para formar a lesão de desmineralização. Os espécimes foram divididos aleatoriamente em 5 grupos (n=11), de acordo com os tratamentos preventivos: 1- Controle (sem tratamento); 2- Verniz fluoretado a 5% Duraphat®; 3- Flúor-gel 1,23%; 4- MI PasteTM; e 5- MI Paste PlusTM. Os tratamentos foram realizados uma vez por semana durante 3 semanas. Nos intervalos das aplicações os espécimes foram submetidos a ciclos de pH (DES/RE) num total de 21 dias. Após a finalização da ciclagem os fragmentos foram seccionados longitudinalmente, sendo que em uma metade foi analisada a microdureza longitudinal, pelo cálculo da variação percentual da dureza e na outra metade foi avaliada a profundidade de desmineralização do esmalte através de microscopia óptica. Para a análise em FTIR, pó do esmalte foi obtido dos espécimes em três diferentes momentos: inicial sem desmineralização da superfície, após a desmineralização por 43 horas e após o tratamento. Para análise da microdureza longitudinal empregou-se a variação da dureza. Os dados foram analisados quanto a sua distribuição, porém como não foram normais realizou-se uma análise não paramétrica comparando grupo contra grupo pelo Mann Whitney test com &alpha;=5%. Para análise da profundidade de desmineralização, como os dados se apresentaram normais e homogêneos, realizou-se a análise de variância a 1 critério e teste Holm- Sidak para comparação das médias com &alpha;=5%. Para análise em FTIR fez-se apenas uma análise descritiva dos dados. Na análise dos dados pode-se observar que houve diferença estatística significante entre o grupo controle (G1) com o grupo flúor-gel (G3) (p<0,05), o qual apresentou menor perda de dureza e menor profundidade de desmineralização. Os grupos 2, 4 e 5 foram similares entre si e com o G1 para as duas propriedades analisadas. Na análise da absorbância nos diferentes comprimentos de onda pode-se observar um padrão similar em todas as amostras; a banda de fosfato inicial foi mais larga e posicionada em número de ondas menores. Após a desmineralização, esta banda ficou mais estreita e deslocada para número de ondas maiores. Esse comportamento se repetiu e foi similar para todos os grupo. Baseado nos resultados obtidos pode-se concluir que nenhum dos tratamentos preventivos realizados foi capaz de inibir o processo de desmineralização ou promover a remineralização em situações de alto risco a cárie, embora o flúor-gel tenha permitido uma evolução mais lenta da desmineralização / The aim of this study was to evaluate different treatments on remineralization of demineralized enamel in a high cariogenic challenge. 55 enamel fragments (4mmX4mmX2mm) flat and polished were used. The specimens were covered with composite exposed only half of the outer surface (2mmX4mm) and then were immersed in acetate buffer solution (pH 4.7) for 43 hours to form the demineralization lesion. The specimens were randomly divided into 5 groups (n = 11) according with the preventive treatments: 1 - Control (no treatment); 2 - 5% fluoride varnish Duraphat ®; 3 - Fluoride-gel 1.23%; 4 - MI PasteTM; and 5 - MI Paste PlusTM. The treatments were carried out once a week for 3 weeks. During intervals and among applications the specimens were subjected to pH cycles (DES / RE) for a total of 21 days. After finished of the cycling, the samples were longitudinally sectioned, and one half in the longitudinal microhardness was analyzed and the other half the depth of enamel demineralization using optical microscopy was evaluated. For data analyzed was calculate the percentage change in the hardness. For FTIR analysis, the enamel powder was obtained from specimens at three different times: without demineralization of the surface, after demineralization for 43 hours and after treatment. Data were analyzed for their distribution, but they were not normal there was a non-parametric analysis comparing group versus group by t test (Mann- Whitney test) with &alpha;= 5%. To analyze the depth of demineralization, as the data were normal and homogeneous, we performed analysis of variance criterion 1 and Holm-Sidak test for comparison of means with &alpha;= 5%. For FTIR was realized of descriptive analysis of the data. Data analyzed showed statistically significant difference between the control group (G1) with the fluoride gel group (G3) (p <0.05), which showed less loss of lower hardness and depth of demineralization. Groups 2, 4 and 5 were similar among them and with G1 for two properties analyzed. The analysis of the absorbance at different wavelengths can be observed a similar pattern in all samples; band initial phosphate was wider and placed on the number of smaller waves. After demineralization, this band became narrower and shifted to higher wave number. This behavior was similar for all groups and it is repeated for every group. Based on the results this study it can be concluded that none of the preventive treatment carried out was able to inhibit the demineralization or promote remineralization in high caries risk situations, although fluoride gel has allowed a slow evolution of demineralization

The Cold-Gas Dynamic-Spray process also known as Cold Spray (CS) has been researched for three decades. The CS process is a solid-state deposition technique via supersonic velocity of powder particles at a temperature significantly below the melting point of the spray material. This thesis presents background on the overall CS process parameters, and additional information on the microstructural and mechanical properties of typical Cold Sprayed materials.This Thesis primarily presents a study on the microstructural annealing response of CS Al 6061. It should be noted that for this study, the term “annealing” is used in the sense of the classical metallurgical definition of annealing, and not a specific temper designation for the 6061 alloy. Cross sections of CS Al 6061 were imaged with a scanning electron microscope (SEM) in secondary electron (SE), backscatter electron (BSE), and electron backscatter diffraction (EBSD) imaging mode for quantitative and qualitative information on the grain size and orientation of the CS microstructure. The detailed SE, BSE and EBSD mode images present the grain size and grain orientation of the original powder, as received (AR) state and after heat treating at 200°C for 1 hour, 10 hours, and 100 hours. Three different regions, characterized with distinctly differing microstructures, are labeled as low, medium, and high deformation regions, and their microstructures, and evolving features are discussed. Vickers microhardness testing are performed to examine the differences in hardness values between different heat treatments, and for correlation with the level of deformation and grain refinement in the microstructure. SEM imaging was used in BSE mode to correlate microhardness variation to the different regions within the CS microstructure.

La technologie de projection plasma sous basse pression a attiré l’attention de nombreux chercheurs comme une nouvelle technique qui permet d’établir un pont entre la projection thermique conventionnelle et le dépôt physique en phase vapeur. Ainsi, cette technologie étend les limites de projection thermique classique et augmente également la vitesse de croissance des dépôts par rapport aux procédés PVD ou CVD classiques. Cette technique peut évaporer totalement ou partiellement les poudres injectées et mener à la réalisation de revêtements à microstructure colonnaire et/ou plus denses, difficiles à réaliser avec des procédés de projection thermique conventionnels. La projection plasma de suspension a été effectuée pour la première fois sous basse pression. L’injection axiale de suspension avec une torche tri-cathodes permet d’augmenter l’échange enthalpique entre le jet de plasma et les poudres après l’évaporation du solvant. La spectroscopie à l’émission optique (OES) a été utilisée pour estimer la température électronique et vérifier l’existence de phase vapeur d’YSZ dans le jet de plasma. Finalement, des revêtements plus denses furent réalisés (comparés à ceux préparés par projection plasma de suspension à pression atmosphérique présentant des particules fondues, agglomérées et de la condensation de vapeur. Des tests de nano-indentation instrumentée ont été effectués sur la surface polie des dépôts réalisés. Les résultats montrent des valeurs de 5,8 GPa pour la dureté et 114,5 GPa pour le module d’élasticité, augmentant de 61% et 31%, respectivement, en comparaison avec les valeurs obtenues par SPS sous atmosphère ambiante. Les essais de projection de poudre YSZ agglomérée ont été réalisés avec une torche F4-VB dans le but de synthétiser une phase vapeur d’YSZ. On observe que les dépôts peuvent se former derrière les échantillons en céramique, sans vis-à-vis du plasma, par condensation de vapeur. En face de cette torche, des revêtements composites ont été obtenus par un mélange de poudres fondues et condensation de vapeur, simultanément. Cependant la quantité de phase vapeur est très faible dans le jet de plasma. Pour comprimer ce jet sous basse pression et afin d’améliorer l’échange d’enthalpie entre le jet de plasma et les poudres injectées, une buse rallongée a été mise en place sur la torche F4-VB. Les revêtements présentent ainsi une microstructure plus dense. Ceci est attribué à la haute vitesse des particules fondues vers le substrat suite à l’utilisation de la buse modifiée. Ce type de revêtement montre une valeur maximale de microdureté Vickers de 1273 Hv100 g. Par ailleurs, la réalisation de dépôts de carbures a été effectuée. Les résultats montrent la possibilité de former des carbures par projection plasma sous basse pression. Les revêtements composites (TiC/Ti) sont déposés par projection plasma réactif sous basse pression en utilisant le méthane comme gaz porteur. La température électronique Te calculée est d’environ 6200 K selon les résultats d’OES, ce qui est supérieur à la température d’ébullition du Ti et de TiC. Le revêtement de Ti pur présente une microstructure dense alors que TiC/Ti présente une microstructure lamellaire. Cependant, la quantité de TiC dans les revêtements est d’environ 20 vol.%. La microdureté Vickers, effectuée sur surface polie, a tendance à diminuer de 846±152 à 773±86 Hv100 g avec l’augmentation de la distance de projection. / As a new technology, the very low pressure plasma spraying has attracted attentions of many researchers, making it possible to establish a bridge between the conventional atmospheric plasma spraying (APS) and the vapor deposition (PVD or CVD). As a result, this new technology enlarges the limitation of APS and increases the deposition rate in comparison with the PVD or CVD. It is possible to evaporate partially the injected material and even evaporate completely and finally realize the columnar or dense coatings from the vapor or the mixture of vapor and liquid. The suspension plasma spraying is performed for the first time at low pressure. Taking consideration of the configuration of the three-cathode torch, the axial injection of the suspension is conducted which can increase the enthalpy change between the plasma jet and the sprayed material. The data of optical emission spectroscopy (OES) could be used to calculate the electron temperature and verify the existence of vapor of YSZ in the plasma jet. Finally, the dense coating was prepared by suspension plasma spraying at low pressure, which is composed of the melted particles, the agglomerated particles and the vapor deposition. The test of nano-indentation is conducted on the polished surface. It shows a value of 5.8 GPa for the microhardness and 114.5 GPa for the elastic modulus, increasing 61% and 31%, respectively, compared with the values obtained by SPS in the ambient atmosphere. In this study, another torch F4-VB is also conducted even of it has a low power in compared with that of O3CP torch. The powder feed rate is reduced to about 1.5 g·min-1 to achieve the vapor of YSZ taking the low power input of the torch into consideration. The columnar structure coating is realized from vapor deposition out of line of sight of projection upon the ceramic tubes. The composite structure coating is deposited by the mixture of melted particles and the vapor deposition simultaneously in front of this torch. But the quantity of vapor of YSZ is low in plasma jet. In order to compress the larger plasma jet and then improve the enthalpy change between the plasma jet and sprayed particles, an extended nozzle is prepared. It shows that the coating has a dense structure, which can be attributed to higher velocity of the melted powders. The coating shows a maximum value of microhardness Vickers up to 1273 Hv100 g. The composite coating of TiC/ Ti is realized by reactive plasma spraying using the methane as the carrier gas. The electron temperature Te is calculated to be 6200 K, which is over the boiling point of TiC and Ti. The coating Ti shows a dense structure and the composite coating TiC/Ti shows a lamellar structure. But the quantity of TiC in the composite coating is very low, about 20 vol.%. The Vickers microhardness is performed on the polished surface. It shows a decreasing tendency from 846 ± 152 to 773 ± 86 Hv100g with the increase of spraying distance. The tribological test is also implemented showing a high value of the coefficient of friction of 0.78 to 0.85, which can lead to a high abrasion. In order to synthesize a larger quantity of TiC in the composite coating, a higher power input torch should be put into action in the future.

Tooth-whitening or tooth-bleaching has become an integral part of modern dental practice. Today, a large number of whitening products are available on the market which are commonly categorized into dentist-supervised home bleaching, in-office bleaching and over-the-counter bleaching products according to their mode of application. This thesis looks into safety and efficacy of various tooth-whitening products and methods.

Tooth-whitening or tooth-bleaching has become an integral part of modern dental practice. Today, a large number of whitening products are available on the market which are commonly categorized into dentist-supervised home bleaching, in-office bleaching and over-the-counter bleaching products according to their mode of application. This thesis looks into safety and efficacy of various tooth-whitening products and methods.

The demanding structural applications (e.g. aerospace, biomedical, etc.) require new materials with improved mechanical performance. The novel Ti-based dendrite + nano-/ultrafine-structured (Ti-based DNUS) composites exhibit an advantageous combination of high compressive strength (2000 – 2500 MPa) and large compressive ductility (10 – 30 %) already in the as-cast state [1,2] and, therefore, can be referred as high-performance materials. However, these Ti-based composites frequently exhibit very low or even lack of tensile ductility [3]. Therefore, the aim of this research work is to develop high strength Ti-based DNUS composites with pronounced tensile plasticity and to correlate the mechanical properties with their microstructure. In order to reach the goal, the high-strength Ti66Nb13Cu8Ni6.8Al6.2 (at.%) alloy exhibiting large compressive ductility [4] was selected for the modification. The microstructure of Ti66Nb13Cu8Ni6.8Al6.2 is composed of two metallographic constituents including β-Ti dendrites and an interdendritic component. The β-Ti dendrites are enriched in Nb and, therefore, Nb is referred as “dendritic element” whereas the interdendritic component is enriched in Ni and Cu and, therefore, these are referred as “interdendritic elements”. To perform a systematic study of the “interdendritic elements” (Ni, Cu and Co) effect on microstructure, a number of alloys with different concentration and types of alloying elements (Ti-Nb-Cu-Ni-Al, Ti-Nb-Co-Ni-Al, Ti-Nb-Cu-Co-Al and Ti-Nb-Ni(Co)-Al) were developed. It was shown that a higher concentration of the “interdendritic elements” in a composition within one alloy system corresponds to a higher volume fraction of the interdendritic component. Additionally, the crystal structure of the interdendritic phases is affected by type of the “interdendritic elements”. Since the most advanced applications (e.g. aerospace) require materials with high specific strengths, the new ductile Ti-Nb-Cu-Ni-Al alloys were modified to reduce their density, i.e. the Nb was substituted by lighter V. As a result, a new family of Ti-V-Cu-Ni-Al alloys with improved specific strength compared to the Ti-Nb-Cu-Ni-Al alloys was developed. Additionally, moduli of resilience of the Ti-V-Ni-Cu-Al alloys are superior when compared with those of the commercial Ti-based spring materials. The effect of microstructure on deformation of the newly developed alloys was studied through the in-situ microstructural analysis of samples at different strained states by means of scanning electron microscopy. To reveal the effect of the metallographic constituents on strength, the microhardness mapping of the new alloys was performed. Using the obtained empirical principles of microstructure adjustment, a new Ti68.8Nb13.6Co6Cu5.1Al6.5 (at.%) alloy with a large static toughness (superior to those of the recently developed Ti-based metallic glass composites) was developed. This large static toughness is due to both high strength and significant tensile plasticity. To study the effect of microstructure on tensile plasticity of Ti68.8Nb13.6Co6Cu5.1Al6.5 the in-situ microstructural analysis of samples at different strained states in the scanning electron microscope as well as the transmission electron microscopy studies were performed. / Der erhöhte Anspruch an strukturelle Anwendungen (z.B. Luftfahrt, Biomedizin, etc.) verlangt neue Werkstoffe mit verbesserten mechanischen Leistungsfähigkeiten. Neuartige Ti-basierte dendritische nano-/ultrafeine Komposite (Ti-basierte DNUS Komposite) besitzen eine vorteilhafte Kombination von hoher Druckfestigkeit mit großer plastischer Verformbarkeit unter Druckbelastung bereits im Gusszustand [1,2] wodurch sie als hochleistungsfähige Werkstoffe angesehen werden. Jedoch besitzen diese Ti-basierte DNUS Komposite heufig eine stark verringerte oder gar keine Duktilität unter Zugbelastung [3]. Deswegen ist es das Ziel dieser Forschungsarbeit neue hochfeste Ti-basierte DNUS Komposite mit ausgeprägter Duktilität unter Zugbelastung zu entwickeln und die mechanischen Eingeschaften mit ihrer Mikrostruktur zu korrelieren. Um dieses Ziel zu erreichen wurde die hochfeste Legierung Ti66Nb13Cu8Ni6.8Al6.2 (at.%) [4], die eine große plastische Verformbarkeit unter Druckbelastung aufweist, ausgewählt. Die Mikrostruktur von Ti66Nb13Cu8Ni6.8Al6.2 setzt sich aus zwei metallographischen Konstituenten, einschließlich β-Ti Dendriten und einer interdendritischen Komponente, zusammen. Die β-Ti Dendriten sind mit Nb angereichert, weswegen Nb als “dendritisches Element” bezeichnet wird, wohingegen die interdendritische Komponente mit Ni und Cu angereichert ist und deswegen diese als “interdendritische Elemente” bezeichnet werden. Um den Einfluss der “interdendritischen Elemente” (Ni, Cu and Co) auf die Mikrostruktur zu untersuchen wurden Legierungen mit verschiedenen Konzentrationen unterschiedlicher Legierungselemente (Ti-Nb-Cu-Ni-Al, Ti-Nb-Co-Ni-Al, Ti-Nb-Cu-Co-Al and Ti-Nb-Ni(Co)-Al) entwickelt. Es wurde gezeigt, dass eine höhere Konzentration “interdendritischer Elemente” in einer bestimmten Zusammensetzung einem höheren Volumanteil der interdendritischen Komponente entspricht. Zusätzlich wird die Kristallstruktur der interdendritischen Phase sehr stark durch die “interdendritischen Elemente” beeinflusst. Da die meisten hoch entwickelten Anwendungen (z.B. Luftfahrt) gesteigerte spezifische Festigkeiten erforden, wurden die neuen duktilen Ti-Nb-Cu-Ni-Al Legierungen modifiziert um ihre Dichte zu reduzieren, indem Nb durch das leichtere V ersetzt wurde. Als Ergebniss wurde eine neue Familie von Ti-V-Cu-Ni-Al Legierungen, mit im Vergleich zu Ti-Nb-Cu-Ni-Al Legierungen verbesserten spezifischen Festigkeiten, entwickelt. Zusäzlich ist die elastische Formänderungsenergiedichte der neu entwickelten Legierungen höher verglichen mit kommerziellen Ti-basierten Federmaterialien. Der Effekt der Mikrostruktur auf das Verformungsverhalten der Legierungen wurde mittels in-situ mikrostruktureller Analysen verschiedener Verformungszustände im Rasterelektronenmikroskop untersucht. Um ein Einfluss der metallographischen Konstituenten auf die Festigkeit zu bestimmen wurden Mikrohärtekarten erstellt. Unter Verwendung der erhalten empirischen Prinzipen zur Einstellung der Mikrostruktur wurde eine neue Legierung Ti68.8Nb13.6Co6Cu5.1Al6.5 (at.%) mit hoher statischer Zähigkeit (besser als die der kürzlich entwickelten Ti-basierten gläsernen metallischen Kompositlegierungen) entwickelt. Diese hohe statische Zähigkeit wird sowohl durch die hohe Festigkeit als auch durch die ausgeprägte Plastizität unter Zugbelastung verursacht. Um den Einfluss der Mikrostruktur auf die Plastizität unter Zug zu untersuchen wurde Transmissionelektronmikroskopie sowie in-situ mikrostrukturelle Analysen verschiedener Verformungszustände im Rasterelektronmikroskop durchgefühlt.

O objetivo do presente trabalho foi avaliar diferentes tratamentos na remineralização do esmalte desmineralizado em situação de alto desafio cariogênico. Foram utilizados 55 fragmentos de esmalte bovino (4mmX4mmX2mm) planificados e polidos. Os espécimes foram cobertos com resina composta ficando exposta apenas a metade da superfície externa (2mmX4mm) e então, foram imersos em solução tampão de acetato (pH 4,7) por 43 horas para formar a lesão de desmineralização. Os espécimes foram divididos aleatoriamente em 5 grupos (n=11), de acordo com os tratamentos preventivos: 1- Controle (sem tratamento); 2- Verniz fluoretado a 5% Duraphat®; 3- Flúor-gel 1,23%; 4- MI PasteTM; e 5- MI Paste PlusTM. Os tratamentos foram realizados uma vez por semana durante 3 semanas. Nos intervalos das aplicações os espécimes foram submetidos a ciclos de pH (DES/RE) num total de 21 dias. Após a finalização da ciclagem os fragmentos foram seccionados longitudinalmente, sendo que em uma metade foi analisada a microdureza longitudinal, pelo cálculo da variação percentual da dureza e na outra metade foi avaliada a profundidade de desmineralização do esmalte através de microscopia óptica. Para a análise em FTIR, pó do esmalte foi obtido dos espécimes em três diferentes momentos: inicial sem desmineralização da superfície, após a desmineralização por 43 horas e após o tratamento. Para análise da microdureza longitudinal empregou-se a variação da dureza. Os dados foram analisados quanto a sua distribuição, porém como não foram normais realizou-se uma análise não paramétrica comparando grupo contra grupo pelo Mann Whitney test com &alpha;=5%. Para análise da profundidade de desmineralização, como os dados se apresentaram normais e homogêneos, realizou-se a análise de variância a 1 critério e teste Holm- Sidak para comparação das médias com &alpha;=5%. Para análise em FTIR fez-se apenas uma análise descritiva dos dados. Na análise dos dados pode-se observar que houve diferença estatística significante entre o grupo controle (G1) com o grupo flúor-gel (G3) (p<0,05), o qual apresentou menor perda de dureza e menor profundidade de desmineralização. Os grupos 2, 4 e 5 foram similares entre si e com o G1 para as duas propriedades analisadas. Na análise da absorbância nos diferentes comprimentos de onda pode-se observar um padrão similar em todas as amostras; a banda de fosfato inicial foi mais larga e posicionada em número de ondas menores. Após a desmineralização, esta banda ficou mais estreita e deslocada para número de ondas maiores. Esse comportamento se repetiu e foi similar para todos os grupo. Baseado nos resultados obtidos pode-se concluir que nenhum dos tratamentos preventivos realizados foi capaz de inibir o processo de desmineralização ou promover a remineralização em situações de alto risco a cárie, embora o flúor-gel tenha permitido uma evolução mais lenta da desmineralização / The aim of this study was to evaluate different treatments on remineralization of demineralized enamel in a high cariogenic challenge. 55 enamel fragments (4mmX4mmX2mm) flat and polished were used. The specimens were covered with composite exposed only half of the outer surface (2mmX4mm) and then were immersed in acetate buffer solution (pH 4.7) for 43 hours to form the demineralization lesion. The specimens were randomly divided into 5 groups (n = 11) according with the preventive treatments: 1 - Control (no treatment); 2 - 5% fluoride varnish Duraphat ®; 3 - Fluoride-gel 1.23%; 4 - MI PasteTM; and 5 - MI Paste PlusTM. The treatments were carried out once a week for 3 weeks. During intervals and among applications the specimens were subjected to pH cycles (DES / RE) for a total of 21 days. After finished of the cycling, the samples were longitudinally sectioned, and one half in the longitudinal microhardness was analyzed and the other half the depth of enamel demineralization using optical microscopy was evaluated. For data analyzed was calculate the percentage change in the hardness. For FTIR analysis, the enamel powder was obtained from specimens at three different times: without demineralization of the surface, after demineralization for 43 hours and after treatment. Data were analyzed for their distribution, but they were not normal there was a non-parametric analysis comparing group versus group by t test (Mann- Whitney test) with &alpha;= 5%. To analyze the depth of demineralization, as the data were normal and homogeneous, we performed analysis of variance criterion 1 and Holm-Sidak test for comparison of means with &alpha;= 5%. For FTIR was realized of descriptive analysis of the data. Data analyzed showed statistically significant difference between the control group (G1) with the fluoride gel group (G3) (p <0.05), which showed less loss of lower hardness and depth of demineralization. Groups 2, 4 and 5 were similar among them and with G1 for two properties analyzed. The analysis of the absorbance at different wavelengths can be observed a similar pattern in all samples; band initial phosphate was wider and placed on the number of smaller waves. After demineralization, this band became narrower and shifted to higher wave number. This behavior was similar for all groups and it is repeated for every group. Based on the results this study it can be concluded that none of the preventive treatment carried out was able to inhibit the demineralization or promote remineralization in high caries risk situations, although fluoride gel has allowed a slow evolution of demineralization