A series of in situ polymerized CNT/PI nanocomposite materials synthesized at a fixed diamine‐to‐dianhydride monomer feed ratio with varying concentrations of added –COOH‐ functionalized CNT is studied. It is found that the glass transition temperature of the nanocomposite varies non‐monotonically with CNT concentration. To determine the origin of this behavior, the molecular weights of the matrix polymers are measured by the intrinsic‐viscosity method. The functional‐group density of the CNT material is determined by potentiometric titration. The results confirm that the glass transition of the CNT/PI system depends on the concentration of the CNT filler through its influence on the functional group stoichiometry and thus on the molecular weight of the polycondensation product.
In this paper, an atomistic model for PI/SiO2 hybrid nanocomposites was designed for the investigation of physical properties of this material on the base of molecular dynamics simulations. The thermal properties of a reference pure PI matrix in the temperature range of 300–650 K were first investigated. The results for the CTE and the glass transition temperature showed good agreement with the experimental data. Then, the thermal expansion of the model of PI/silica composite material with different SiO2 fractions was investigated at normal conditions. The CTE of the composite model decreases with the increase in the SiO2 content in agreement with experimental studies. The results show a threshold for the SiO2 loading beyond which the material model exhibits ultra‐low thermal expansion.
Continuous depth sensing indentation microhardness measurements were performed to investigate the effect of filler content and dimensionality on the mechanical behaviour of different polymer nanocomposites. In 1D filler reinforced nanocomposites (such as PP/MWCNT system), both the hardness and the indentation modulus were found to appreciably increase up to a filler weight fraction of 1.6 wt.-%. Further addition of the filler changed the properties only insignificantly. In the nanocomposites with 2D filler (such as in PA6/LS) both the hardness and the indentation modulus increase notably with the addition of the filler and showed intense plasticity. In the investigated systems and composition range, the 3D filler (such as PP/OS2) showed no reinforcing effect at all. In was concluded that the 1D and 2D nanofillers play much more effective reinforcing role to improve the mechanical properties than the 3D fillers. 相似文献
This study reveals the influence of silica nanoparticles on the cure reactions of a diglycidyl ether of bisphenol A epoxy resin. As soon as the silica nanoparticles are added to the neat resin (1, 3, and 5 vol.‐%), the total degree of conversion increases with an increasing amount of nanoparticles, and the cure reaction shows a more complex autocatalytic behaviour, which can not be described by a traditional kinetic model. Results from subsequent thermo‐mechanical analyses confirm an alteration in the microstructure attributable only to the presence of the nanoparticles in the curing stage. An amino‐rich interphase around the reactive treated particles is formed, which shifts the resin/hardener ratio, and benefits the homopolymerization of the epoxy and leads to a more highly crosslinked epoxy network. At the same time, the nanophase consists of a core‐shell structure with the rigid particle inside and a rubber‐like shell because of the excess hardener in this region.
TEM image of two neighboring silica nanoparticles in the epoxy matrix showing a 2–3 nm altered interphase region. 相似文献
Summary: This investigation presents a simultaneous and convenient approach to produce a high‐performance polyimide with a low dielectric constant by introducing the octa‐acrylated polyhedral oligomeric silsesquioxane (methacrylated‐POSS) into a polyimide matrix to form polyimide semi‐interpenetrating polymer network (semi‐IPN) nanocomposites. The differential scanning calorimetry (DSC) and Fourier‐transform infrared (FT‐IR) results indicate that the self‐curing of methacrylated‐POSS and the imidization of polyamic acid (PAA) occurs simultaneously. The morphology of a semi‐IPN structure of polyimide/POSS‐PI/POSS nanocomposites with POSS nanoparticles embedded inside the matrix is elucidated. The POSS particles are uniform and are aggregated to a size of approximately 50–60 nm inside the polyimide matrix. The interconnected POSS particles are observed at high POSS content. The structure is highly cross‐linked, so the PI/POSS nanocomposites have an enhanced glass transition temperature. The high porosity of the PI/POSS nanocomposites markedly reduces the dielectric constant of PI because of the nanometer‐scale porous structure of POSS.
FT‐IR spectra of the various compounds of A) methacrylate‐POSS before curing, B) methacrylate‐POSS after curing, C) PAA containing 15 wt.‐% POSS, and D) PI/POSS containing 15 wt.‐% POSS. 相似文献
This study investigates the feasibility of a novel nanocomposite (GC/Ag) of a genipin-crosslinked chitosan (GC) film in which was embedded various amounts of Ag nanoparticles for wound-dressing applications. In situ UV-vis results revealed that adding chitosan solution did not affect the characteristics of Ag nanoparticles. The water uptake ratios and surface hydrophilicity of the GC/Ag nanocomposite were better and the degradation rates slightly lower than those of the pure GC film. The presence of Ag nanoparticles enhanced L929 cell attachment and growth. Its function as an anti-microbial agent in a GC/Ag nanocomposite was assessed for Ag contents of over 100 ppm. In conclusion, silver ions had dual functions--structural reinforcement and provision of antimicrobial properties to a biocompatible polymer. 相似文献
The properties of polymers near an interface are altered relative to their bulk value due both to chemical interaction and geometric confinement effects. For the past two decades, the dynamics of polymers in confined geometries (thin polymer film or nanocomposites with high‐surface area particles) has been studied in detail, allowing progress to be made toward understanding the origin of the dynamic effects near interfaces. Observations of mechanical property enhancements in polymer nanocomposites have been attributed to similar origins. However, the existing measurement methods of these local mechanical properties have resulted in a variety of conflicting results on the change of mechanical properties of confined polymers. Here, an atomic force microscopy (AFM)‐based method is demonstrated that directly measures the mechanical properties of polymers adjacent to a substrate with nanometer resolution. This method allows us to consistently observe the gradient in mechanical properties away from a substrate in various materials systems, and paves the way for a unified understanding of thermodynamic and mechanical response of polymers. This gradient is both longer (up to 170 nm) and of higher magnitude (50% increase) than expected from prior results. Through the use of this technique, we will be better able to understand how to design polymer nanocomposites and polymeric structures at the smallest length scale, which affects the fields of structures, electronics, and healthcare.
The crystallization behavior and structure of polyamide 6 (PA6) nanocomposites containing 3 wt.‐% montmorillonite (MMT) were investigated for different cooling conditions using differential scanning calorimetry and X‐ray diffraction. In sharp contrast to PA6 and other semicrystalline polymers, increased cooling rates resulted in higher crystallinity of PA6/MMT. The highest crystallinity (60.8%) occurred in the liquid nitrogen‐quenched PA6/MMT film. The results show that the γ‐crystalline form is dominant in the rapidly cooled PA6/MMT. 相似文献
The effect of the addition of two combined fillers, smectite clay and diamond and smectite clay and carbon nanoparticles, on structure, morphology, isothermal and non isothermal crystallization behaviour, tensile and thermal properties of isotactic polypropylene (iPP) has been investigated by using several techniques: wide angle X-ray diffraction, optical and scanning electron microscopy, thermogravimetry, differential scanning calorimetry and tensile techniques. It was found that nanoparticles of diamond and carbon favour the nucleation of the β-form of iPP crystal, whereas the clay nanolayers do not have any influence on the crystal structure of iPP. The thermal stability of iPP/(clay+diamond) and iPP/(clay+carbon) is improved with respect to neat iPP, whereas no influence is detected when only clay is added to iPP. At the given crystallization conditions, the overall crystallization peak of iPP/(clay+diamond) almost exactly overlaps the crystallization peak of neat iPP, whereas in the case of iPP/clay and iPP/(clay+carbon) the maximum of the crystallization peaks is shifted to higher temperature. The spherulite growth rate, G values do not differ from one another. The iPP/(clay+carbon) system shows ductile behavior. The other systems show brittle behavior with failure before necking. These results were related with the very high percentage of beta phase present in the samples of iPP/(clay+carbon). 相似文献
Summary: Pristine FH is incorporated into a PS matrix by melt blending with and without latex precompounding of PS and FH. Direct melt blending results in microcomposites, whereas the latex‐mediated (masterbatch) technique results in PS/FH nanocomposites. The tensile creep response of the micro‐ and nanocomposites are determined in short‐term creep tests. The resistance to creep is improved with increasing dispersion of FH in the PS matrix. Master curves (creep compliance vs. time), constructed based on isothermal creep tests performed in the temperature range between 5 and 45 °C, show that the FH reinforcement affects mostly the initial creep compliance (interphase effect). On the other hand, the stable creep is matrix (bulk) dominated. It is established that the Williams‐Landel‐Ferry equation is fairly applicable to the creep results.
Scheme of the change of creep compliance as a function of time for micro‐ and nanocomposites with an amorphous matrix. 相似文献
Polymer/layered silicate nanocomposite thin films were developed as clear, transparent coatings. Laponite‐S, which is a synthetic layered clay, was dispersed in a polyethylene oxide matrix and solution cast onto glass slides for further testing. Rheological properties, wear abrasion resistance, and scratch resistance were tested for each sample to examine the nanoparticle dispersion effects on the materials' properties. In this study, we identify and characterize the materials to be used, establish the appropriate conditions for the preparation of polymer/Laponite nanocomposite dispersions, illustrate methods for the development of PEO/Laponite‐S films, and characterize the films. Results on the rheological behavior of PEO‐silicate nanocomposites as a function of Laponite solids loading and PEO concentration, as well as some preliminary wear abrasion properties of the films are presented in this study. 相似文献
Summary: Migration of clay to the surface of nylon 6‐organically modified clay is investigated. The effect of annealing time and temperature on the migration of the clay is reported. Attenuated total reflectance FT‐IR spectrometry, X‐ray diffraction, and high‐resolution electronic microscopy are used in this study. The results obtained indicate that migration occurs predominantly in the samples with exfoliated structure. Migration increases in the temperature range of 250–275 °C. A further increase in temperature decreases the extent of migration. Migration increases with time at 250 °C. Annealing in the presence of oxygen decreases migration. It is suggested that the extent of migration depends on the concentration of the surfactant and the polymer in the exfoliated particles.
High‐resolution electronic microscopy image of an exfoliated nylon‐6/clay sample in which migration has occurred. 相似文献
Summary: In this work, a surface re-modified multi-walled carbon nanotube (MWNT) was prepared by the chemical attachment of oligomeric unsaturated polyester on the MWNT surface. The re-modified MWNT was incorporated in two concentrations of 0.35 and 0.70 Wt.% into epoxy resin in order to investigate its effect on morphology and mechanical behavior of the MWNT/epoxy nanocomposite. The transmission electron microscopy showed that the re-modification of MWNT surface improves its dispersion state in the epoxy matrix. The tensile measurements for the nanocomposite having different amounts of surface re-modified/not-modified MWNT showed that the fracture mechanism changed from brittle to tough beyond a certain amount of surface re-modified MWNT. The scanning electron microscopy findings on the fracture surface morphology of the resulted nanocomposite substantiated the observed phenomena. 相似文献
Films of particulate polyimide-silica hybrids were produced by a sol-gel process and were examined in terms of morphological structure and fracture properties at different temperatures, varying from 20 to 250 °C. The fracture toughness characteristics were studied by the “Essential Work of Fracture” method using double edge-notched specimens of different ligament lengths. The results showed that the fracture toughness, expressed through the essential (we) and non-essential work of fracture (βwp) parameters increased when submicron silica particles were dispersed in the polyimide matrix. In particular, it was found that both we and βwp increased with temperature to a larger extent than the parent polyimide. This enhancement in the fracture toughness was attributed to extensive cavitations and shear yielding originating at the particle interface and within the matrix. 相似文献
A continuum model is developed to investigate the microstructure‐dependent AC properties of MWCNT/polymer nanocomposites. The AC conductivity of the composite is increased by a higher curl ratio of MWCNTs. At a critical frequency ω0, the AC conductivity switches to a frequency‐dependent region. For high MWCNT content, the curl curliness of MWCNTs has only a weak influence on the AC conductivity. For medium MWCNT content, the AC conductivity became frequency‐dependent for low frequencies with decreasing curl ratio of MWCNTs, which cannot be explained by correlation length theory. An interpretation based on the linear circuit theory is given. With increasing size of MWCNT clusters, the critical frequency ω0 increases. It is also affected significantly by the crystallinity the polymer.
