999 resultados para Flexural resistance


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A major difficulty to achieve maximum weight savings in the manufacture of composite structural components, is the tendency of these materials have the formation of voids and cracks in the interior and surface components. In aeronautical applications, controlling the volume fraction of fibers, resins and empty the components of composite is very hard. In this work, composites of epoxy matrix RTM6 reinforced with NCF (non crimp fabric carbon) processed by resin transfer molding (RTM) were characterized for porosity (P-ap) and density (rho(ad)). We used a method based on Archimedes' principle (ASTM C830) and the technique of helium pycnometer. The porosity values were compared with those determined by acid digestion (ASTM D3171). The mechanical properties of processed composites was evaluated by testing on the performing flexural and the results were correlated with the porosity value. All techniques tested to determine void content are satisfactory. The differents results can be justified for heterogeneous void distribution on laminate and differences among techniques characteristics. (C) 2011 Published by Elsevier Ltd. Selection and/or peer-review under responsibility of ICM11

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The aim of this study is to evaluate the flexural resistance of three types of restorative materials: compomer (Freedom), resin-modified glass-ionomer (Vitremer) and composite resin (Esthet-X), observing whether the application of bleaching agent can cause alterations of their flexural properties. Sixty samples were made using a 10 x 1 x 1 mm brass mold, and divided into three groups: G1- Freedom (SDI); G2- Vitremer (3M ESPE); G3- Esthet-X (Dentsply). On half of the samples of each group (10 samples) the bleaching treatment was applied and the other half used as control, was stored in distilled water at a temperature of 37 degrees C. Whiteness HP Maxx bleaching system was applied on the sample surface following the manufacturer's recommendations, simulating the bleaching treatment at the clinic. After this period, a flexural strength (three-point bending) test was conducted using (EMIC DL 1000) machine until the samples fractured. The data were submitted to ANOVA and Tukey tests. Of the restorative materials studied, G3-(87.24 +/- 31.40 MPa) presented the highest flexural strength, followed by G1-(61.67 +/- 21.32 MPa) and G2-(61.67 +/- 21.32 MPa). There was a statistical difference in flexural strength after the bleaching treatment. It was concluded that the use of a beaching agent can promote significant alteration of the flexural strength of these restorative materials.

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The purpose of this study was to evaluate the impact of different disinfection solutions on flexural resistance of chemically-activated acrylic resin. Test pieces were made of clear acrylic resin using a rectangular mold and employing two techniques: wet polymerization under pressure (n = 20) and dry polymerization under pressure (n = 20). Test pieces were subdivided into four equal groups: distilled water (control), sodium bicarbonate, 1% sodium hypochlorite and effervescent ats. The 30-day cycling technique consisted of immersing the test pieces in 100 ml of solution for 10 min three times a day and placing them in closed containers containing artificial saliva at 37°C. Subsequently, the flexural resistance of samples was tested. Data were analyzed using two-way analysis of variance (ANOVA) with forces serving as the dependent variables and the polymerization technique and cleaning agents as independent variables. Post hoc multiple comparisons were performed using Tukey’s test. There was no statistically significant difference in the flexural strength between the two polymerization techniques. The greatest flexural strength was observed for the effervescent tablets group followed by the control and 1% sodium hypochlorite groups which were statistically similar. Thus, the sodium bicarbonate solution caused the lowest flexural resistance of the test pieces.

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Avaliou-se a influência de dois sistemas de acabamento e polimento na resistência à flexão de uma cerâmica feldspática EX-3 (Noritake). Para isto, confeccionou-se blocos cerâmicos com medidas em conformidade com a ISO 6872/1995. Em seguida obteve-se o glaze natural. A padronização da rugosidade superficial foi conferida com auxílio de um rugosímetro, e os blocos foram então divididos em cinco grupos. O Grupo I (controle) foi testado com glaze. Para os testes realizados nos demais grupos, os blocos receberam um tratamento de asperização por meio de uma ponta diamantada 4137 (KG Sorensen). Em seguida foram polidos com diferentes protocolos. No grupo II, o sistema de polimento dura white (Shofu). No grupo III, o sistema de polimento dura white (shofu) associado a uma pasta diamantada aplicada com disco de feltro. No grupo IV o sistema de polimento Exa Cerapol (Edenta) e no grupo V, este mesmo sistema mais pasta diamantada aplicada com disco de feltro. Após os procedimentos de acabamento e polimento, foi avaliada a rugosidade conseguida (Ra), para se avaliar a eficácia dos métodos testados. A análise estatística por ANOVA (p ≤ 0,05) mostrou não haver diferença estatisticamente significante entre os grupos (G2=3,820,58; G3=3,550,61; G4=4,050,40; G5=3,950.47) . Feito isto, os corpos-de-prova foram submetidos a um ensaio mecânico de resistência à flexão em três pontos, e também neste caso, os resultados depois de tratados estatisticamente não demonstraram diferenças estatísticas entre os grupos glazeados e os grupos que receberam tratamento (G1=132,126,9 MPa; G2=123,317,4 MPa; G3=114,519,3 MPa; G4=104,211,9 MPa e G5=104,719,1 MPa) . Após a realização destas avaliações, tornou-se possível concluir que o uso dos sistemas de acabamento e polimento testados neste trabalho permite obter superfícies com rugosidade similar a obtida com o glaze natural e não interferem na resistência à flexão da cerâmica utilizada.

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Recentemente, foram lançados no mercado odontológico novos materiais estéticos para restaurações diretas em dentes posteriores, aos quais são atribuídas propriedades mais adequadas para essa indicação. Entretanto, as informações disponíveis são ainda muito escassas, gerando dúvidas quanto à sua real eficácia, sobre quais as diferenças de suas composições e propriedades físicas e mecânicas em relação aos materiais até então disponíveis e se, de fato, apresentam melhor performance clínica. Em vista do exposto, nos propusemos a estudar contração de polimerização, resistência à flexão e concentração de partículas inorgânicas, por massa e volume, de sete resinas compostas (Alert, Ariston, Solitaire, Definite, Filtek P60, Z-100 e Tetric Ceram). A contração de polimerização foi medida nos materiais inseridos em um anel plástico, e o registro das alterações, durante a polimerização, foi feito por meio de instrumento eletrônico de medida linear, que registra as alterações dimensionais, com sensibilidade de 1 mm. A resistência à flexão foi medida na máquina de ensaios mecânicos MTS 810 e a confecção dos corpos-de-prova e dos dispositivos para o ensaio foi orientada pela norma ISO no 4049:1988. A determinação do conteúdo de partículas inorgânicas por massa foi feita através da pesagem de uma porção de resina composta polimerizada antes e após a eliminação da fase orgânica em forno, à temperatura de 700oC. O porcentual volumétrico de partículas inorgânicas foi calculado com base no Princípio de Arquimedes. Foi determinado o volume da resina composta polimerizada, antes e após a eliminação da fase orgânica, pela diferença da massa do material pesado ao ar e imerso em água. Os dados de conteúdo de partículas inorgânicas por massa e por volume, de contração de polimerização e resistência à flexão foram submetidos...(Resumo completo, clicar acesso eletrônico abaixo)

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Pós-graduação em Engenharia Civil - FEIS

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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

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The main reasons for the attention focused on ceramics as possible structural materials are their wear resistance and the ability to operate with limited oxidation and ablation at temperatures above 2000°C. Hence, this work is devoted to the study of two classes of materials which can satisfy these requirements: silicon carbide -based ceramics (SiC) for wear applications and borides and carbides of transition metals for ultra-high temperatures applications (UHTCs). SiC-based materials: Silicon carbide is a hard ceramic, which finds applications in many industrial sectors, from heat production, to automotive engineering and metals processing. In view of new fields of uses, SiC-based ceramics were produced with addition of 10-30 vol% of MoSi2, in order to obtain electro conductive ceramics. MoSi2, indeed, is an intermetallic compound which possesses high temperature oxidation resistance, high electrical conductivity (21·10-6 Ω·cm), relatively low density (6.31 g/cm3), high melting point (2030°C) and high stiffness (440 GPa). The SiC-based ceramics were hot pressed at 1900°C with addition of Al2O3-Y2O3 or Y2O3-AlN as sintering additives. The microstructure of the composites and of the reference materials, SiC and MoSi2, were studied by means of conventional analytical techniques, such as X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive spectroscopy (SEM-EDS). The composites showed a homogeneous microstructure, with good dispersion of the secondary phases and low residual porosity. The following thermo-mechanical properties of the SiC-based materials were measured: Vickers hardness (HV), Young’s modulus (E), fracture toughness (KIc) and room to high temperature flexural strength (σ). The mechanical properties of the composites were compared to those of two monolithic SiC and MoSi2 materials and resulted in a higher stiffness, fracture toughness and slightly higher flexural resistance. Tribological tests were also performed in two configurations disco-on-pin and slideron cylinder, aiming at studying the wear behaviour of SiC-MoSi2 composites with Al2O3 as counterfacing materials. The tests pointed out that the addition of MoSi2 was detrimental owing to a lower hardness in comparison with the pure SiC matrix. On the contrary, electrical measurements revealed that the addition of 30 vol% of MoSi2, rendered the composite electroconductive, lowering the electrical resistance of three orders of magnitude. Ultra High Temperature Ceramics: Carbides, borides and nitrides of transition metals (Ti, Zr, Hf, Ta, Nb, Mo) possess very high melting points and interesting engineering properties, such as high hardness (20-25 GPa), high stiffness (400-500 GPa), flexural strengths which remain unaltered from room temperature to 1500°C and excellent corrosion resistance in aggressive environment. All these properties place the UHTCs as potential candidates for the development of manoeuvrable hypersonic flight vehicles with sharp leading edges. To this scope Zr- and Hf- carbide and boride materials were produced with addition of 5-20 vol% of MoSi2. This secondary phase enabled the achievement of full dense composites at temperature lower than 2000°C and without the application of pressure. Besides the conventional microstructure analyses XRD and SEM-EDS, transmission electron microscopy (TEM) was employed to explore the microstructure on a small length scale to disclose the effective densification mechanisms. A thorough literature analysis revealed that neither detailed TEM work nor reports on densification mechanisms are available for this class of materials, which however are essential to optimize the sintering aids utilized and the processing parameters applied. Microstructural analyses, along with thermodynamics and crystallographic considerations, led to disclose of the effective role of MoSi2 during sintering of Zrand Hf- carbides and borides. Among the investigated mechanical properties (HV, E, KIc, σ from room temperature to 1500°C), the high temperature flexural strength was improved due to the protective and sealing effect of a silica-based glassy phase, especially for the borides. Nanoindentation tests were also performed on HfC-MoSi2 composites in order to extract hardness and elastic modulus of the single phases. Finally, arc jet tests on HfC- and HfB2-based composites confirmed the excellent oxidation behaviour of these materials under temperature exceeding 2000°C; no cracking or spallation occurred and the modified layer was only 80-90 μm thick.