Search Results (8)

Results obtained in physics, chemistry and materials science on nanoparticles have drawn significant interest in the use of nanostructures on dental implants. The main focus concerns nanoscale surface modifications of titanium-based dental implants in order to increase the surface roughness and provide a better bone–implant interfacial area. Surface coatings via the sol–gel process ensure the deposition of a homogeneous layer of nanoparticles or mixtures of nanoparticles on the titanium substrate. Nanotubular structures created on the titanium surface by anodic oxidation yield an interesting nanotopography for drug release. Carbon-based nanomaterials hold great promise in the field of dentistry on account of their outstanding mechanical properties and their structural characteristics. Carbon nanomaterials that include carbon nanotubes, graphene and its derivatives (graphene oxide and graphene quantum dots) can be used as coatings of the implant surface. Their antibacterial properties as well as their ability to be functionalized with adequate chemical groups make them particularly useful for improving biocompatibility and promoting osseointegration. Nevertheless, an evaluation of their possible toxicity is required before being exploited in clinical trials. Full article

The reinforcement of elastomers is essential in the rubber industry in order to obtain the properties required for commercial applications. The addition of active fillers in an elastomer usually leads to an improvement in the mechanical properties such as the elastic modulus and the rupture properties. Filled rubbers are also characterized by two specific behaviors related to energy dissipation known as the Payne and the Mullins effects. The Payne effect is related to non-linear viscoelastic behavior of the storage modulus while the Mullins or stress-softening effect is characterized by a lowering in the stress when the vulcanizate is extended a second time. Both effects are shown to strongly depend on the interfacial adhesion and filler dispersion. The basic mechanisms of reinforcement are first discussed in the case of conventional rubber composites filled with carbon black or silica usually present in the host matrix in the form of aggregates and agglomerates. The use of nanoscale fillers with isotropic or anisotropic morphologies is expected to yield much more improvement than that imparted by micron-scale fillers owing to the very large polymer–filler interface. This work reports some results obtained with three types of nanoparticles that can reinforce rubbery matrices: spherical, rod-shaped and layered fillers. Each type of particle is shown to impart to the host medium a specific reinforcement on account of its own structure and geometry. The novelty of this work is to emphasize the particular mechanical behavior of some systems filled with nanospherical particles such as in situ silica-filled poly(dimethylsiloxane) networks that display a strong polymer–filler interface and whose mechanical response is typical of double network elastomers. Additionally, the potential of carbon dots as a reinforcing filler for elastomeric materials is highlighted. Different results are reported on the reinforcement imparted by carbon nanotubes and graphenic materials that is far below their expected capability despite the development of various techniques intended to reduce particle aggregation and improve interfacial bonding with the host matrix. Full article

The mechanical properties of polymeric materials are strongly affected by molecular orientation occurring under processing conditions. Infrared dichroism is particularly well suited for characterizing polymer chain orientation at a molecular level. The usefulness of this technique has been demonstrated through various applications in homopolymers, semi-crystalline polymers, copolymers, polymer blends, as well as in polymer composites. Determination of molecular orientation can be carried out in the mid- and near-infrared ranges and very small dichroic effects can be detected with the use of a photoelastic modulator. Chain orientation in polymer composites is seen to increase with the filler content in the case of a strong interface between the two phases, making possible a quantification of the degree of bonding between the host polymeric matrix and the incorporated inclusions. Full article

Vibrational spectroscopies, including infrared and Raman techniques, are important tools for the characterization of chemical composition, molecular structures, and chain orientation under mechanical deformation of polymeric materials. The development of fiber-optic-based spectrometers has broadened the use of vibrational spectroscopy for process monitoring in various fields including polymerization, curing, and manufacturing processes. Combined with chemometrics, near-infrared (NIR) spectroscopy is now recognized as one of the most important techniques for polymer analyses. Infrared and Raman studies also offer invaluable means for the analysis of inorganic particles used as reinforcing fillers for polymers. The characterization of surface species and the nature of interfacial bonding between the organic and inorganic phases are important issues for the understanding of composite properties. Infrared spectroscopy is particularly convenient for the detection and analysis of hydroxyl groups on filler surfaces, and Raman spectroscopy is particularly well suited for the study of carbon-based materials. In both techniques, polymer-filler interactions can be evidenced through frequency shifts or width changes of bands associated with vibrational modes of functional groups of either macromolecular chains or filler particles. Selected examples of application of infrared and Raman spectroscopies illustrate their potential for monitoring polymer processes, measuring polymer orientation, and characterizing polymer composites. Full article

This paper reviews studies carried out on natural rubber filled with nanofillers such as spherical silica particles (generated by the sol gel reaction), clays and carbon nanostructures. It is shown that the mechanical response of NR is influenced by several parameters including the processing conditions, the state of filler dispersion, the polymer-filler interactions and the filler morphological aspects. Even if the sol gel process conducted in vulcanized rubber yields almost ideal dispersions, rod-shaped particles such as clay, carbon fibers or carbon nanotubes are by far more efficient in terms of mechanical reinforcement on account of their anisotropic character and their ability to orientate in the direction of stretch. The efficiency of layered fillers such as clays or graphitic structures clearly depends on the way they are dispersed (exfoliated) in the rubber. Complete exfoliation still remains difficult to achieve which limits the tremendous nanoreinforcement expected from a single layer of clay or graphite. In all cases, the onset of crystallization is observed at a lower strain value than that of the unfilled matrix due to strain amplification effects. Full article

Due to the growing interest in nanocomposites, a molecular characterization of these materials is essential for the understanding of their properties and for the development of new materials. Spectroscopic techniques that bring information at a molecular level are unavoidable when characterizing polymers, fillers and composites. Selected examples of the application of fluorescence, solid-state nuclear magnetic resonance (NMR), infrared and Raman spectroscopies, illustrate the potential of these techniques for the analysis of the filler surface, the evaluation of the state of filler dispersion in the host matrix, the extent of interaction between the polymer and the filler particles or the dynamics of polymer chains at the polymer–filler interface. Full article

Carbon nanostructures including carbon black, carbon nanotubes, graphite or graphene have attracted a tremendous interest as fillers for elastomeric compounds. The preparation methods of nanocomposites that have a strong impact on the state of filler dispersion and thus on the properties of the resulting composites, are briefly described. At a same filler loading, considerable improvement in stiffness is imparted to the host polymeric matrix by the carbon nanomaterials with regard to that provided by the conventional carbon black particles. It is mainly attributed to the high aspect ratio of the nanostructures rather than to strong polymer-filler interactions. The orienting capability of the anisotropic fillers under strain as well the formation of a filler network, have to be taken into account to explain the high level of reinforcements. A comparison of the efficiency of the different carbon nanostructures is carried out through their mechanical and electrical properties but no clear picture can be obtained since the composite properties are strongly affected by the state of filler dispersion. Full article

Carbon-based nanomaterials have emerged as a subject of enormous scientific attention due to their outstanding mechanical, electrical and thermal properties. Incorporated in a polymeric matrix, they are expected to significantly improve physical properties of the host medium at extremely small filler content. In this work, we report a characterization of various carbonaceous materials by Raman spectroscopy that has become a key technique for the analysis of different types of sp² nanostructures, including one-dimensional carbon nanotubes, two-dimensional graphene and the effect of disorder in their structures. The dispersion behavior of the D and G’ Raman bands, that is, their shift to higher frequencies with increasing laser excitation energy, is used to assess the interfacial properties between the filler and the surrounding polymer in the composites. Full article