An Overview of Functionalized Graphene Nanomaterials for Advanced Applications

Interest in the development of graphene-based materials for advanced applications is growing, because of the unique features of such nanomaterials and, above all, of their outstanding versatility, which enables several functionalization pathways that lead to materials with extremely tunable properties and architectures. This review is focused on the careful examination of relationships between synthetic approaches currently used to derivatize graphene, main properties achieved, and target applications proposed. Use of functionalized graphene nanomaterials in six engineering areas (materials with enhanced mechanical and thermal performance, energy, sensors, biomedical, water treatment, and catalysis) was critically reviewed, pointing out the latest advances and potential challenges associated with the application of such materials, with a major focus on the effect that the physicochemical features imparted by functionalization routes exert on the achievement of ultimate properties capable of satisfying or even improving the current demand in each field. Finally, current limitations in terms of basic scientific knowledge and nanotechnology were highlighted, along with the potential future directions towards the full exploitation of such fascinating nanomaterials.

Insights into the Microstructural Evolution Occurring during Pyrolysis of Metal-Modified Ceramers Studied through Selective SiO2 Removal

Silicon oxycarbide ceramers containing 5% aluminum, zirconium, and cobalt with respect to the total Si amount are prepared from a commercial polysiloxane and molecular precursors and pyrolyzed at temperatures ranging from 500 to 1000 °C. HF etching is carried out to partially digest the silica phase, thus revealing structural characteristics of the materials, which depend upon the incorporated heteroatom. From the structural and textural characterization, it was deduced that when Al enters into the ceramer structure, the crosslinking degree is increased, leading to lower carbon domain size and carbon incorporation as well. On the contrary, the substitution by Zr induced a phase-separated SiO2-ZrO2 network with some degree of mesoporosity even at high pyrolysis temperatures. Co, however, forms small carbidic crystallites, which strongly modifies the carbonaceous phase in such a way that even when it is added in a small amount and in combination with other heteroatoms, this transient metal dominates the structural characteristics of the ceramer material. This systematic study of the ceramer compounds allows the identification of the ultimate properties of the polymer-derived ceramic composites.

Variation of Ultimate Properties in Extruded iPP-Mesoporous Silica Nanocomposites by Effect of iPP Confinement within the Mesostructures

Nanocomposites based on isotactic polypropylene (iPP) and mesoporous silica particles of either MCM-41 or SBA-15 were prepared by melt extrusion. The effect of the silica incorporated into an iPP matrix was firstly detected in the degradation behavior and in the rheological response of the resultant composites. Both were ascribed, in principle, to variations in the inclusion of iPP chains within these two mesostructures, with well different pore size. DSC experiments did not provide information on the existence of confinement in the iPP-MCM-41 materials, whereas a small endotherm, located at about 100 °C and attributed to the melting of confined crystallites, is clearly observed in the iPP-SBA-15 composites. Real-time variable-temperature Small Angle X-ray Scattering (SAXS) experiments with synchrotron radiation turned out to be crucial to finding the presence of iPP within MCM-41 pores. From these measurements, precise information was also deduced on the influence of the MCM-41 on iPP long spacing since overlapping does not occur between most probable iPP long spacing peak with the characteristic diffractions from the MCM-41 hexagonal nanostructure in comparison with existing superposition in SBA-15-based materials.

Synthesis and Properties of Tung Oil-Based Unsaturated Co-Ester Resins Bearing Steric Hindrance

New tung oil (TO)-based, unsaturated, co-ester (Co-UE) macromonomers bearing steric hindrance were synthesized by modifying a TO-based maleate (TOPERMA) monomer with an anhydride structure with hydroxyethyl methacrylate (HEMA) and methallyl alcohol (MAA), respectively. The obtained Co-UE monomers (TOPERMA-HEMA and TOPERMA-MAA) were then characterized by 1H NMR and gel permeation chromatography (GPC). For comparison, hydroxyethyl acrylate (HEA)-modified TOPERMA (TOPERMA-HEA) was also synthesized and characterized. Subsequently, the obtained Co-UEs were thermally cured with styrene, and the ultimate properties of the resulting materials were studied. It was found that by introducing the structure of steric hindrance into the TO-based Co-UE monomer, the tensile strength and Young’s modulus of the resulting materials were improved. Furthermore, by reducing the length of the flexible chain in the Co-UE monomer, the tensile strength, Young’s modulus, and glass transition temperature (Tg) of the resultant materials were also improved. The TOPERMA-MAA resin gave the best performance in these TO-based Co-UE resins, which showed a tensile strength of 32.2 MPa, Young’s modulus of 2.38 GPa, and Tg of 130.3 °C. The developed ecofriendly materials show promise in structural plastic applications.

Characterization of High Porous PZT Piezoelectric Ceramics by different Techniques

Ultimate properties of a porous ceramic is highly process dependent. In this study, prevalent porous ceramics fabrication methods (Freeze casting, Foam reticulation and Burnable Plastic Sphere (BURPS) method) have been compared by fabricating the porous lead zirconate titanate (PZT) based piezoelectric ceramics. Field Emission Scanning electron microscopy (FESEM) studies were carried out to study the pore size and distribution of the ceramics. Hydrostatic co-efficients increased tremendously on incorporation of porosity which led to Hydrostatic Figure of Merit of 7480 in Foam reticulation samples (porosity 86%). The three dimensionally interconnected networks in the freeze casted samples led to lowest acoustic impedance (6 MRayls) despite not having the lowest density.

Effect of thermal treatment on the mechanical and viscoelastic response of polypropylenes incorporating a β nucleating agent

The influence of two thermal treatments on the structure, morphology, and ultimate properties exhibited by isotactic polypropylene (iPP), synthesized by conventional Ziegler–Natta iPP (Z-iPP) or metallocene iPP (m-iPP) catalysts, has been investigated in the present work. Novelty of this research consisted in the incorporation of a β nucleating agent in two different contents to the m-iPP. Results attained are compared with those found in the Z-iPP and important differences are observed. Differential scanning calorimetry and X-ray diffraction experiments revealed that coexistence of different crystalline lattices took place depending on the type of iPP: β and α forms were found in the β nucleated Z-iPP specimens, whereas α, β, and γ polymorphs could be developed in the m-iPP with nucleating agent. On the other hand, the iPP glass transition temperature ( Tg) did not exhibit a significant change because of the addition of β nucleant, as deduced from Dynamic Mechanical Thermal Analysis (DMTA) analysis. Moreover, the size and shape of the iPP spherulites was totally changed by the presence of the β agent. This nucleant promoted the formation of smaller spherulites in a greater amount, as demonstrated by optical microscopy. Concerning the mechanical parameters, microhardness, MH, and Young modulus, E, values were in the fast crystallized samples lower than those presented by their slowly cooled counterparts. A good balance in properties was seen for the slowly crystallized m-iPP that incorporated a 5 wt% content in β nucleating agent, this fact being ascribed to the coexistence of the three α, β, and γ polymorphs.

Research and Development of Rubber Bearings for Sodium-Cooled Fast Reactor: Ultimate Properties of Half-Scale Thick Rubber Bearings Based on Breaking Tests

This paper describes the results of static loading tests using a half-scale thick rubber bearing to investigate ultimate properties application for a sodium-cooled-fast-reactor (SFR). Thick rubber bearings which have a rubber layer that is roughly two times thicker in comparison with existing rubber bearings have been developed by the authors to ensure seismic safety margins for components installed in the reactor building, and to reduce the seismic response in the vertical direction as well as the horizontal direction. The thick rubber bearings, 1600 mm in diameter at the full scale, have been designed to provide a rated load of about 10,000 kN, at the compressive stress of 5.0 MPa, with a horizontal natural period of 3.4 s and a vertical natural period of about 0.133 s. The restoring-force characteristics, including variations, and breaking points, for the thick rubber bearings have not been cleared yet. These validations are essential from the point of view of probabilistic risk assessment (PRA) for a base-isolated nuclear plant as well as a verification of the structural integrity of the thick rubber bearings. The purpose of this paper is to indicate the variation of the stiffness and damping ratios for restoring force characteristics, and the breaking strain or stress, as ultimate properties through static loading tests using half-scale thick rubber bearings. In addition, an analytical model for the thick rubber bearings which is able to express the nonlinear restoring force, including the breaking points, is presented.