135,964 research outputs found

    Piezoelectric composite materials

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    A laminated structural devices has the ability to change shape, position and resonant frequency without using discrete motive components. The laminate may be a combination of layers of a piezoelectrically active, nonconductive matrix material. A power source selectively places various levels of charge in electrically conductive filaments imbedded in the respective layers to produce various configurations in a predetermined manner. The layers may be electrically conductive having imbedded piezoelectrically active filaments. A combination of layers of electrically conductive material may be laminated to layers of piezoelectrically active material

    LDEF fiber-composite materials characterization

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    Degradation of a number of fiber/polymer composites located on the leading and trailing surfaces of LDEF where the atomic oxygen (AO) fluences ranged from 10(exp 22) to 10(exp 4) atoms/cm(sup 2), respectively, was observed and compared. While matrices of the composites on the leading edge generally exhibited considerable degradation and erosion-induced fragmentation, this 'asking' process was confined to the near surface regions because these degraded structures acted as a 'protective blanket' for deeper-lying regions. This finding leads to the conclusion that simple surface coatings can significantly retard AO and other combinations of degrading phenomena in low-Earth orbit. Micrometeoroid and debris particle impacts were not a prominent feature on the fiber composites studied and apparently do not contribute in a significant way to their degradation or alteration in low-Earth orbit

    Strengthening of foamed composite materials

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    We investigate the shear elastic modulus of soft polymer foams loaded with hard spherical particles and we show that, for constant bubble size and gas volume fraction, strengthening is strongly dependent on the size of those inclusions. Through an accurate control of the ratio λ\lambda that compares the particle size to the thickness of the struts in the foam structure, we evidence a transition in the mechanical behavior at λ1\lambda \approx 1. For λ<1\lambda < 1, every particle loading leads to a strengthening effect whose magnitude depends only on the particle volume fraction. On the contrary, for λ>1\lambda > 1, the strengthening effect weakens abruptly as a function of λ\lambda and a softening effect is even observed for λ10\lambda \gtrsim 10. This transition in the mechanical behavior is reminiscent of the so-called "particle exclusion transition" that has been recently reported within the framework of drainage of foamy granular suspensions [Haffner B, Khidas Y, Pitois O. The drainage of foamy granular suspensions. J Colloid Interface Sci 2015. In Press.]. It involves the evolution for the geometrical configuration of the particles with respect to the foam network, and it appears to control the mechanics of such foamy systems

    Self-lubricating composite materials

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    The mechanical properties of two types of self lubricating composites (polymer matrix composites and inorganic composites) are discussed. Specific emphasis is given to the applicability of these composites in the aerospace industry

    Environmental effects on composites for aircraft

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    The influence of the operational environment on the behavior of composite materials and aircraft components fabricated with these composite materials was considered. Structural weight savings, manufacturing cost savings, and long-term environmental durability are among the factors examined. The flight service experience to date of composite components is evaluated. In addition, the influence of a number of worldwide, ground based outdoor exposures on the physical and mechanical properties of six composite materials is discussed. In particular, the current extent of the ultraviolet surface degradation and the moisture gained by diffusion is shown

    Flame-retardant composite materials

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    The properties of eight different graphite composite panels fabricated using four different resin matrices and two types of graphite reinforcement are described. The resin matrices included: VPSP/BMI, a blend of vinylpolystyryl pyridine and bismaleimide; BMI, a bismaleimide; and phenolic and PSP, a polystyryl pyridine. The graphite fiber used was AS-4 in the form of either tape or fabric. The properties of these composites were compared with epoxy composites. It was determined that VPSP/BMI with the graphite tape was the optimum design giving the lowest heat release rate

    Synthesis of Supported Catalysts by Dry Impregnation in Fluidized Bed

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    The synthesis of catalytic or not composite materials by dry impregnation in fluidized bed is described. This process can be carried out under mild conditions from solutions of organometallic precursors or colloidal solutions of preformed nanoparticles giving rise to reproducible metallic nanoparticles containing composite materials with a high reproducibility. The adequate choice of the reaction conditions makes possible to deposit uniformly the metal precursor within the porous matrix or on the support surface. When the ratio between the drying time and the capillary penetration time (tsec/tcap) is higher than 10, the impregnation under soft drying conditions leads to a homogeneous deposit inside the pores of the particles of support. The efficiency of the metal deposition is close to 100%, and the size of the formed metal nanoparticles is controlled by the pores diameter. Finally, some of the presented composite materials have been tested as catalysts: iron-based materials were used in carbon-nanotubes synthesis, while Pd and Rh composite materials have been investigated in hydrogenation reactions

    Spontaneously formed porous and composite materials

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    In recent years, a number of routes to porous materials have been developed which do not involve the use of pre-formed templates or structure-directing agents. These routes are usually spontaneous, meaning they are thermodynamically downhill. Kinetic control, deriving from slow diffusion of certain species in the solid state, allows metastable porous morphologies rather than dense materials to be obtained. While the porous structures so formed are random, the average architectural features can be well-defined, and the porosity is usually highly interconnected. The routes are applicable to a broad range of functional inorganic materials. Consequently, the porous architectures have uses in energy transduction and storage, chemical sensing, catalysis, and photoelectrochemistry. This is in addition to more straightforward uses deriving from the pore structure, such as in filtration, as a structural material, or as a cell-growth scaffold. In this feature article, some of the methods for the creation of porous materials are described, including shape-conserving routes that lead to hierarchical macro/mesoporous architectures. In some of the preparations, the resulting mesopores are aligned locally with certain crystallographic directions. The coupling between morphology and crystallography provides a macroscopic handle on nanoscale structure. Extension of these routes to create biphasic composite materials are also described
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