Showing papers on "Polymer nanocomposite published in 2008"

Functionalized graphene sheets for polymer nanocomposites

Abstract: Polymer-based composites were heralded in the 1960s as a new paradigm for materials. By dispersing strong, highly stiff fibres in a polymer matrix, high-performance lightweight composites could be developed and tailored to individual applications. Today we stand at a similar threshold in the realm of polymer nanocomposites with the promise of strong, durable, multifunctional materials with low nanofiller content. However, the cost of nanoparticles, their availability and the challenges that remain to achieve good dispersion pose significant obstacles to these goals. Here, we report the creation of polymer nanocomposites with functionalized graphene sheets, which overcome these obstacles and provide superb polymer-particle interactions. An unprecedented shift in glass transition temperature of over 40 degrees C is obtained for poly(acrylonitrile) at 1 wt% functionalized graphene sheet, and with only 0.05 wt% functionalized graphene sheet in poly(methyl methacrylate) there is an improvement of nearly 30 degrees C. Modulus, ultimate strength and thermal stability follow a similar trend, with values for functionalized graphene sheet- poly(methyl methacrylate) rivaling those for single-walled carbon nanotube-poly(methyl methacrylate) composites.

Effects of particle size, particle/matrix interface adhesion and particle loading on mechanical properties of particulate–polymer composites

Abstract: There have been a number of review papers on layered silicate and carbon nanotube reinforced polymer nanocomposites, in which the fillers have high aspect ratios. Particulate–polymer nanocomposites containing fillers with small aspect ratios are also an important class of polymer composites. However, they have been apparently overlooked. Thus, in this paper, detailed discussions on the effects of particle size, particle/matrix interface adhesion and particle loading on the stiffness, strength and toughness of such particulate–polymer composites are reviewed. To develop high performance particulate composites, it is necessary to have some basic understanding of the stiffening, strengthening and toughening mechanisms of these composites. A critical evaluation of published experimental results in comparison with theoretical models is given.

Stimuli-Responsive Polymer Nanocomposites Inspired by the Sea Cucumber Dermis

Abstract: Sea cucumbers, like other echinoderms, have the ability to rapidly and reversibly alter the stiffness of their inner dermis. It has been proposed that the modulus of this tissue is controlled by regulating the interactions among collagen fibrils, which reinforce a low-modulus matrix. We report on a family of polymer nanocomposites, which mimic this architecture and display similar chemoresponsive mechanic adaptability. Materials based on a rubbery host polymer and rigid cellulose nanofibers exhibit a reversible reduction by a factor of 40 of the tensile modulus, for example, from 800 to 20 megapascals (MPa), upon exposure to a chemical regulator that mediates nanofiber interactions. Using a host polymer with a thermal transition in the regime of interest, we demonstrated even larger modulus changes (4200 to 1.6 MPa) upon exposure to emulated physiological conditions.

Tunneling effect in a polymer/carbon nanotube nanocompositestrain sensor

Abstract: A strain sensor has been fabricated from a polymer nanocomposite with multiwalled carbon nanotube (MWNT) fillers. The piezoresistivity of this nanocomposite strain sensor has been investigated based on an improved three-dimensional (3D) statistical resistor network model incorporating the tunneling effect between the neighboring carbon nanotubes (CNTs), and a fiber reorientation model. The numerical results agree very well with the experimental measurements. As compared with traditional strain gauges, much higher sensitivity can be obtained in the nanocomposite sensors when the volume fraction of CNT is close to the percolation threshold. For a small CNT volume fraction, weak nonlinear piezoresistivity is observed both experimentally and from numerical simulation. The tunneling effect is considered to be the principal mechanism of the sensor under small strains.

Electrical energy storage in ferroelectric polymer nanocomposites containing surface-functionalized BaTiO3 nanoparticles

Abstract: Polymer nanocomposites were prepared using surface-functionalized BaTiO3 nanoparticles and ferroelectric polymers. The nanocomposites based on the polymer with a higher permittivity exhibit larger electric displacements under the applied fields, thereby leading to higher energy densities. An energy density of 7 J/cm3 has been achieved in a nanocomposite containing 30 vol % BaTiO3 at 150 MV/m, representing an impressive ∼120% enhancement in comparison with that in the neat polymer.

The mechanisms leading to the useful electrical properties of polymer nanodielectrics

Abstract: Polymer nanocomposites with metal oxide nanoparticle fillers exhibit enhanced electrical breakdown strength and voltage endurance compared to their unfilled or micron filled counterparts. This paper presents the following hypothesis for the mechanisms leading to improved properties. The inclusion of nanoparticles provides myriad scattering obstacles and trap sites in the charge carriers' paths, effectively reducing carrier mobility and thus carrier energy. The result is homocharge buildup at the electrodes, which increases the voltage required for further charge injection due to blocking by the homocharge. The hypothesis is supported by electroluminescence, pulsed electro acoustic analysis, thermally stimulated current measurements, a comparison of AC, DC, and impulse breakdown, as well as absorption current measurements, in silica/crosslinked polyethylene matrix composites with supporting evidence from titania/epoxy composites.

The amount of immobilized polymer in PMMA SiO$_{2}$ nanocomposites determined from calorimetric data

Abstract: For semicrystalline polymers there is an ongoing debate at what temperature the immobilized or rigid amorphous fraction (RAF) devitrifies (relaxes). The question if the polymer crystals aremelting first and simultaneously theRAFdevitrifies or the RAF devitrifies first and later on the crystals melt cannot be answered easily on the example of semicrystalline polymers. This is because the crystals, which are the reason for the immobilization of the polymer, often disappear (melt) in the same temperature range as theRAF. For polymer nanocomposites the situation is simpler. Silica nanoparticles do notmelt or undergo other phase transitions altering the polymer–nanoparticle interaction in the temperature range where the polymer is thermally stable (does not degrade). The existence of an immobilized fraction in PMMA SiO2 nanocomposites was shown on the basis of heat capacitymeasurements at the glass transition of the polymer. The results were verified by enthalpy relaxation experiments below the glass transition. The immobilized layer is about 2 nm thick at low filler content if agglomeration is not dominant. The thickness of the layer is similar to that found in semicrystalline polymers and independent from the shape of the nanoparticles. Nanocomposites therefore offer a unique opportunity to study the devitrification of the immobilized fraction (RAF) without interference of melting of crystals as in semicrystalline polymers. It was found that the interaction between the SiO2 nanoparticles and the PMMA is so strong that no devitrification occurs before degradation of the polymer. No gradual increase of heat capacity or a broadening of the glass transitionwas found. The cooperatively rearranging regions (CRR) are either immobilized or mobile. No intermediate states are found. The results obtained for the polymer nanocomposites support the view that the reason for the restricted mobility must disappear before the RAF can devitrify. For semicrystalline polymers this means that rigid crystals must melt before the RAF can relax. 2007 Elsevier Ltd. All rights reserved.

The electrical properties of polymer nanocomposites with carbon nanotube fillers

Abstract: The electrical properties of polymer nanocomposites containing a small amount of carbon nanotube (CNT) are remarkably superior to those of conventional electronic composites. Based on three-dimensional (3D) statistical percolation and 3D resistor network modeling, the electrical properties of CNT nanocomposites, at and after percolation, were successfully predicted in this work. The numerical analysis was also extended to investigate the effects of the aspect ratio, the electrical conductivity, the aggregation and the shape of CNTs on the electrical properties of the nanocomposites. A simple empirical model was also established based on present numerical simulations to predict the electrical conductivity in several electronic composites with various fillers. This investigation further highlighted the importance of theoretical and numerical analyses in the exploration of basic physical phenomena, such as percolation and conductivity in novel nanocomposites.

The electrical properties of polymer nanocomposites with carbon nanotube fillers

Abstract: The electrical properties of polymer nanocomposites containing a small amount of carbon nanotube (CNT) are remarkably superior to those of conventional electronic composites. Based on three-dimensional (3D) statistical percolation and 3D resistor network modeling, the electrical properties of CNT nanocomposites, at and after percolation, were successfully predicted in this work. The numerical analysis was also extended to investigate the effects of the aspect ratio, the electrical conductivity, the aggregation and the shape of CNTs on the electrical properties of the nanocomposites. A simple empirical model was also established based on present numerical simulations to predict the electrical conductivity in several electronic composites with various fillers. This investigation further highlighted the importance of theoretical and numerical analyses in the exploration of basic physical phenomena, such as percolation and conductivity in novel nanocomposites.

Nanofiller‐reinforced polymer nanocomposites

Abstract: In this work, the technology of nano- and micro-scale particle reinforcement concerning various polymeric fiber-reinforced systems including polyamides (PAs), polyesters, polyurethanes (PUs), polypropylenes (pps), and high-performance/temperature engineering polymers such as polyimide (PI), poly(ether ether ketone) (PEEK), polyarylacetylene (PAA), and poly p-phenylene benzobisoxazole (PBO) is reviewed. When the diameters of polymer fiber materials are shrunk from micrometers to submicrons or nanometers, there appear several unique characteristics such as very large surface area to volume ratio (this ratio for a nanofiber can be as large as 103 times of that of a microfiber), flexibility in surface functionalities and superior mechanical performance (such as stiffness and tensile strength) compared to any other known form of the material. While nanoparticle reinforcement of fiber-reinforced composites has been shown to be a possibility, much work remains to be performed in order to understand how nanoreinforcement results in dramatic changes in material properties. The understanding of these phenomena will facilitate their extension to the reinforcement of more complicated anisotropic structures and advanced polymeric composite systems. Copyright © 2008 John Wiley & Sons, Ltd.

Determination of the stiffness of cellulose nanowhiskers and the fiber-matrix interface in a nanocomposite using Raman spectroscopy

Abstract: The stiffness of 10 nm diameter cellulose nanowhiskers is reported. These whiskers are produced by acid hydrolysis. These whiskers are dispersed in epoxy resin and placed on the surface of a beam of the same material and deformed in tension and compression using a four-point bending device. By following the molecular deformation of the whiskers using Raman spectroscopy it is shown that, by theoretical models of their dispersion and matrix reinforcement, their stiffness can be derived. The effects of debonding, matrix yielding, and buckling of whiskers are also discussed using this method as a means for studying nanocomposite materials.

High-conductivity polymer nanocomposites obtained by tailoring the characteristics of carbon nanotube fillers

Abstract: We present a detailed study of the influence of carbon nanotube (CNT) characteristics on the electrical conductivity of polystyrene nanocomposites produced using a latex-based approach. We processed both industrially-produced multi-wall CNT (MWCNT) powders and MWCNTs from vertically-aligned films made in-house, and demonstrate that while the raw CNTs are individualized and dispersed comparably within the polymer matrix, the electrical conductivity of the final nanocomposites differs significantly due to the intrinsic characteristics of the CNTs. Owing to their longer length after dispersion, the percolation threshold observed using MWCNTs from vertically-aligned films is five times lower than the value for industrially-produced MWCNT powders. Further, owing to the high structural quality of the CNTs from vertically-aligned films, the resulting composite films exhibit electrical conductivity of 103 S m−1 at 2 wt% CNTs. On the contrary, composites made using the industrially-produced CNTs exhibit conductivity of only tens of S m−1. To our knowledge, the measured electrical conductivity for CNT/PS composites using CNTs from vertically-aligned films is by far the highest value yet reported for CNT/PS nanocomposites at this loading.

Carbon Nanotube−Polymer Nanocomposite Infrared Sensor

Abstract: The infrared photoresponse in the electrical conductivity of single-walled carbon nanotubes (SWNTs) is dramatically enhanced by embedding SWNTs in an electrically and thermally insulating polymer matrix. The conductivity change in a 5 wt % SWNT-polycarbonate nanocomposite is significant (4.26%) and sharp upon infrared illumination in the air at room temperature. While the thermal effect predominates in the infrared photoresponse of a pure SWNT film, the photoeffect predominates in the infrared photoresponse of SWNT-polycarbonate nanocomposites.

Silver on PEG-PU-TiO2 Polymer Nanocomposite Films: An Excellent System for Antibacterial Applications

Abstract: Silver impregnated on polymer-titania nanocomposite films exhibit excellent antibacterial properties with the added advantage of repeated use. The polyethylene glycol-polyurethane-titania designated as PEG-PU-TiO2 polymer nanocomposite films were synthesized by simple solution casting technique. Silver has been incorporated into these films by photochemical reduction of silver nitrate solution. The TiO2 facilitated the UV photoreduction of AgNO3 to Ag, which is active as an antibacterial agent. Fourier Transformed Infrared Spectroscopy (FT-IR) confirms the formation of the polymer, polyurethane. X-ray Diffraction (XRD) determined the structure and scanning electron microscopy (SEM), the morphology of the films. XPS confirms the Ag to be in zero oxidation state and the amount of silver impregnated in the films as estimated by scanning electron microscopy−energy-dispersive X-ray analysis (SEM-EDAX), and atomic absorption spectroscopy (AAS) is about 2−4 at %. The antibacterial properties of these films were ...

Nanoscale Ionic Materials

Abstract: Within the general field of polymer grafted or “hairy” nanoparticles, nanoscale ionic materials (NIMs), consisting of a soft polymeric canopy bound to a well-defined nanoparticle core by an ionic bond, occupy a growing niche. They are the first example of neat, self-suspended fluids of nanoparticles (i.e., in the absence of a suspending medium). As such, the perennial dispersion challenges associated with polymer nanocomposites are minimized while the dynamic nature of the ionic bonds provides opportunities for self-healing behavior. Combining the properties of ionic liquids, charged colloid suspensions, and well-dispersed nanocomposites, this new materials platform offers remarkable versatility for current and future applications. This perspective covers techniques and current challenges in synthesis, discusses the state of understanding of the theory behind their structure and properties, and examines successes and future prospects in application in a number of areas, notably in energy-related technologies.

Functionally graded Nylon-11/silica nanocomposites produced by selective laser sintering

Abstract: Selective laser sintering (SLS), a layered manufacturing-based freeform fabrication approach was explored for constructing three-dimensional structures in functionally graded polymer nanocomposites. Here, we report on the processing and properties of functionally graded polymer nanocomposites of Nylon-11 filled with 0–10% by volume of 15 nm fumed silica nanoparticles. SLS processing parameters for the different compositions were developed by design of experiments (DOE). The densities and micro/nanostructures of the nanocomposites were examined by optical microscopy and transmission electron microscopy (TEM). The tensile and compressive properties for each composition were then tested. These properties exhibit a nonlinear variation as a function of filler volume fraction. Finally, two component designs exhibiting a one-dimensional polymer nanocomposite material gradient were fabricated. The results indicate that particulate-filled functionally graded polymer nanocomposites exhibiting a one-dimensional composition gradient can be successfully processed by SLS to produce three-dimensional components with spatially varying mechanical properties.

Biobased Nanocomposites Prepared by In Situ Polymerization of Furfuryl Alcohol with Cellulose Whiskers or Montmorillonite Clay

Abstract: In this work, we employed an in situ polymerization approach to produce polyfurfuryl alcohol (PFA) nanocomposites without the use of solvents or surfactants. On the one hand, furfuryl alcohol (FA) has a dual function, serving both as an effective dispersant for the cellulose whisker (CW) and montmorillonite clay (MMT) nanoparticles and as the matrix precursor for the in situ polymerization. On the other hand, the CW and MMT nanoparticles also serve multiple functions, by first catalyzing the polymerization of FA, and then acting as an effective matrix modifier, increasing the thermal stability of the consolidated PFA nanocomposite. In the case of CW-PFA nanocomposites, the polymerization is catalyzed by sulfonic acid residues at the CW surface, left over from the whisker preparation. In the case of MMT-PFA nanocomposites, the polymerization is catalyzed by Lewis acid sites inherent to the MMT surface. Thermal analysis showed that both types of polymer nanocomposites (PNCs) were characterized by significan...

Permittivity and tan delta characteristics of epoxy nanocomposites in the frequency range of 1 MHz-1 GHz

Abstract: To achieve a compact and reliable design of electrical equipment for the present day requirements, there is an urgent need for better and smart insulating materials and in this respect, the reported enhancements in dielectric properties obtained for polymer nanocomposites seems to be very encouraging. To further understand the dielectric behavior of polymer nanocomposites, this experimental work reports the trends of dielectric permittivities and tan delta (loss tangent) of epoxy nanocomposites with single nano-fillers of Al2O3 and TiO2at low filler concentrations (0.1%, 0.5%, 1% & 5%) over a frequency range of 1 MHz-1 GHz. Results show that the nanocomposites demonstrate some very different dielectric characteristics when compared to those for polymer microcomposites. Unlike the usual expectations of increasing permittivity with increasing filler concentration in polymer microcomposites, it has been seen that up to a certain nano-filler concentration and depending on the permittivity of the nano-filler, the permittivities of the epoxy nanocomposites are less than that of the unfilled epoxy at all the measured frequencies. This suggests that there is a very strong dependence of the filler concentration and nano-filler permittivity on the final permittivity of the nanocomposites at all these frequencies. But, in the case of tan delta behavior in nanocomposites, significant effects of filler concentrations were not observed with both Al2O3 and TiO2 fillers. Tan delta values in nanocomposites with Al2O3 fillers are found to be marginally lower at all filler concentrations when compared with the value for unfilled epoxy. But, in TiO2Oepoxy nanocomposites, although the variations in tan delta are not significant with respect to unfilled epoxy, some interesting trends are observed with respect to the frequencies of measurement.

One-Pot Synthesis of Robust Core/Shell Gold Nanoparticles

Abstract: A one-pot synthesis of thermally stable core/shell gold nanoparticles (Au-NPs) was developed via surface-initiated atom transfer radical polymerization (ATRP) of n-butyl acrylate (BA) and a dimethacrylate-based cross-linker. The higher reactivity of the cross-linker enabled the formation of a thin cross-linked polymer shell around the surface of the Au-NP before the growth of linear polymer chains from the shell. The cross-linked polymer shell served as a robust protective layer, prevented the dissociation of linear polymer brushes from the surfaces of Au-NPs, and provided the Au-NPs excellent thermal stability at elevated temperature (e.g., 110 degrees C for 24 h). This synthetic method could be easily expanded for preparation of other types of inorganic/polymer nanocomposites with significantly improved stability.

Studies of structural, thermal and electrical behavior of polymer nanocomposite electrolytes

Abstract: Structural, thermal and electrical behavior of polymer-clay nanocomposite electrolytes consisting of polymer (polyethylene oxide (PEO)) and NaI as salt with different concentrations of organically modified Na + montmorillonite (DMMT) filler have been investigated. The formation of nanocomposites and changes in the structural properties of the materials were investigated by X-ray diffraction (XRD) analysis. Complex impedance analysis shows the existence of bulk and material-electrode interface properties of the composites. The relative dielectric constant (er) decreases with increase in frequency in the low frequency region whereas frequency independent behavior is observed in the high frequency region. The electrical modulus representation shows a loss feature in the imaginary component. The relaxation associated with this feature shows a stretched exponential decay. Studies of frequency dependence of dielectric and modulus formalism suggest that the ionic and polymer segmental motion are strongly coupled manifeasting as peak in the modulus (M") spectra with no corresponding feature in dielectric spectra. The frequency dependence of ac (alternating current) conductivity obeys Jon- scher power law feature in the high frequency region, where as the low frequency dispersion indicating the presence of electrode polarization effect in the materials.