The properties of synthetic hydrogels can be tuned to address the needs of many tissue‐culture applications. This work characterizes the swelling and mechanical properties of thiol‐ene crosslinked PEG hydrogels made with varying prepolymer formulations, demonstrating that hydrogels with a compressive modulus exceeding 600 kPa can be formed. The amount of peptide incorporated into the hydrogel is shown to be proportional to the amount of peptide in the prepolymer solution. Cell attachment and spreading on the surface of the peptide‐functionalized hydrogels is demonstrated. Additionally, a method for bonding distinct layers of cured hydrogels is used to create a microfluidic channel.
Organoclay–polyolefin nanocomposites have been shown to exhibit slightly increased thermal stability and decreased flammability, compared to unfilled polyolefins. In contrast, we find that when the clay has not been organically modified, the resulting polyolefin nanocomposites are less thermally stable and, unexpectedly, also much less flammable. In this contribution, we investigate the mechanistic origins of these effects. Clay–polyolefin nanocomposites were prepared by in situ polymerization of ethylene or propylene, using a catalyst adsorbed onto the clay. Decreased thermal stability is attributed to clay‐catalyzed polymer decomposition, while decreased flammability arises in part from clay‐catalyzed formation of a polyaromatic char from olefins trapped in the material by the dispersed nanofiller.
CNT based elastomer‐hybrid‐nanocomposites prepared by melt mixing have been investigated showing promising results in technologically relevant electrical, mechanical, and fracture‐mechanical properties. It is demonstrated that the incorporation of CNT in silica‐filled natural rubber results in a good dispersion of the CNT. The materials show an enhanced mechanical stiffness and tensile strength, an increased modulus, and a high electrical conductivity with quite low amounts of CNT, though the tear resistance under dynamical loading is slightly reduced. Using DMA and dielectric spectra, a better understanding of the conduction mechanism, the polymer/tube interaction, and the filler networking in CNT nanocomposites is achieved.
pCBT/MWCNT nanocomposites were prepared by in situ polymerization of CBT after solid‐phase HEBM of the polymerization catalyst containing CBT with MWCNT. The crystallinity and crystallization behavior of the pCBT nanocomposites were studied by WAXS and DSC. The MWCNTs did not affect the crystallinity of the isothermally produced pCBT significantly, but acted as nucleation agents during the crystallization of pCBT from its melt. pCBT/MWCNT nanocomposites were subjected to DMTA, static flexure, and dynamic Charpy impact tests. The flexural modulus, strength, and impact strength from these tests all went through a maximum as a function of the MWCNT content. Optimum properties were found in the MWCNT range of 0.25–0.5 wt.‐%.
Nanocomposites of linear low‐density polyethylene (LLDPE), with three different amounts of polyhedral oligomeric silsesquioxanes (POSS), were prepared through melt‐mixing in a batch‐mixer at 150 °C. The structure of the prepared nanocomposites was studied by X‐ray scattering and optical microscopy. The surface morphology of the nanocomposites was investigated through field‐emission SEM. The thermal properties of the pure LLDPE and nanocomposites were studied by differential scanning calorimeter (DSC). Thermomechanical properties were assessed on a Paar‐Physics MCR501 rheometer using a solid‐state rectangular fixture. Results exhibited a significant improvement in both the storage and loss moduli of the neat LLDPE upon the incorporation of the POSS particles. A substantial improvement in thermal stability was also observed in the high‐temperature region.
Novel nanocomposites prepared by melt mixing of MWCNTs in a hot‐melt adhesive PCL‐based polyurethane are investigated. The nucleating effect of MWCNTs and the confinement they cause to polymer chains are considered. The broadening of the glass transition is indicative of a growth of the immobilized amorphous fraction adhered to MWCNTs. In the molten state the formation of a combined polymer/MWCNT network is observed. Practical requisites of hot melt adhesives, such as adequate melting temperature, crystallization degree, and viscosity are preserved when MWCNTs are added. Improvement of strength at room temperature and welding rate during cooling, are observed.
Unfilled and MWCNT‐filled PA fibers are prepared and the effect of the extensional flow on their mechanical performance and morphological variations is investigated. Morphological analyses using SEM, TEM, and SAXS suggest a stronger orientation of the MWCNTs along the fiber direction with increasing extensional flow. A particular MWCNT bundle formation in the PA drawn nanocomposite fibers is observed for the first time, and a pull‐out of the central nanotube in some bundles is noted. The maintenance of the “shish‐kebab” structure upon extensional flow is responsible for the mechanical improvements and dimensional stability in MWCNT‐filled PA fibers.
Nanocomposites based on an amorphous copolyester (PCTG) were obtained by melt mixing, changing the screw speed and the nature of the surfactant, which differed in polarity and molecular volume. Using Young's modulus as a measure of the dispersion level, a less‐polar nature and a higher molecular volume of the surfactant appeared as positive structural factors for dispersion of the clay in the less‐polar PCTG. The Cloisite 20A, which led to the highest modulus (widest dispersion), was mixed at different contents with PCTG at the observed optimum screw speed (200 rpm). Intercalated structures were observed by WAXD and TEM. The dispersion was wide, as observed by TEM, and led to a large (77%) modulus increase after 7% organoclay addition and to important increases in both tensile yield stress and dimensional stability in creep.
The influence of the functionalization of fully condensed POSS cages on the properties of POM‐based nanocomposites is studied. POSS with different organic substituents [glycidylethyl, aminopropylisobutyl, and poly(ethylene glycol)] are taken into account and melt mixed with POM. Good dispersion was achieved upon the addition of amino functionalized POSS, leading to an increase on the thermal decomposition temperature under nitrogen atmosphere up to 50 °C. However, µm‐size aggregates were observed for other nanocomposites. There is no significant change in other thermal properties of the nanocomposites. The relationships among these effects and the morphological characteristics of the systems were analyzed.
Fully exfoliated PS/clay nanocomposites were prepared via FRP in dispersion. Na‐MMT clay was pre‐modified using MPTMS before being used in a dispersion polymerization process. The objective of this study was to determine the impact of the clay concentrations on the monomer conversion, the polymer molecular weight, and the morphology and thermal stability of the nanocomposites prepared via dispersion polymerization. DLS and SEM revealed that the particle size decreased and became more uniformly distributed with increasing clay loading. XRD and TEM revealed that nanocomposites at low clay loading yielded exfoliated structures, while intercalated structures were obtained at higher clay loading.
Isotactic PP nanocomposites filled with Fe@FeO nanoparticles are fabricated by a facile ex situ method. The nanofillers are dispersed in a boiling PP/xylene solution. X‐ray diffraction is used to determine the nanofiller effects on the crystallinity of PP. The crystallinity along the (040) plane is found to decrease with the incorporation of nanoparticles. Thermal properties and crystallinity are studied by TGA and DSC, respectively. Enhanced thermal stability and influenced crystallinity are observed in the PP nanocomposites compared with those of pure PP. An increased dielectric property without percolation threshold is observed. In addition, the nanocomposites are found to exhibit ferromagnetic properties.
1, 2, 3, 5, and 7.5 wt% MWCNTs are incorporated into PS in a twin‐screw extruder at varying speeds, throughputs and extruder barrel temperatures. Increased SME at enhanced processing speeds seems to have the single largest effect in enhancing dispersion. A relative evaluation of PS/MWCNT interactions indicate an interfacial layer growth of 24% for 2 wt% MWCNT at 1100 rpm compared to 18% growth at 500 rpm. Raman analysis does not show an MWCNT peak shift but a constant increase in FWHM is observed irrespective of the MWCNT content. A significant enhancement of thermal stability occurs up to 2 wt% MWCNT loading while 1–2 wt% shows the rheological threshold. The volume resistivity decreases dramatically in a 2 wt% sample processed at 1100 rpm compared to those processed at 500 rpm.
Morphological analyses of nanocomposites based on TPU and polyhedral oligomeric silsesquioxanes (POSS) was performed using different techniques (transmission electron microscopy, small‐ and wide‐angle X‐ray scattering, differential scanning calorimetry) as a function of molecular weight of poly(ethylene glycol) (PEG) and PEG/POSS mol ratio. A strong interdependence in crystallisation behaviour between the two (POSS and the soft segments of TPU) specified to be able to crystallise in TPU/POSS was found. The mechanical properties determined by using recording microindentation techniques at room temperature were significantly improved by POSS for two material formulations.
Sunflower oil‐based HBTPU/Ag and LTPU/Ag nanocomposites have been prepared by in situ catalytic reduction of a silver salt. The virgin polymer and their nanocomposites are soluble in various polar organic solvents and amenable for both solution‐casting and hot pressing. XRD, TEM, and UV spectroscopic analyses ascertained well‐dispersed, narrow‐sized Ag nanoparticles. Tensile testing, dynamic mechanical, thermogravimetric, and DSC analyses showed desirable mechanical and thermal features with improvement upon incorporation of Ag nanoparticles and the presence of a hyperbranched component in the nanocomposites. RSM has been used to evaluate the catalytic efficacy of the nanocomposites.
To improve the physical properties of poly(trimethylene terephthalate) (PTT), a series of nanocomposites based on PTT and exfoliated graphite (EG) are prepared via melt compounding and their structures, thermal stabilities, mechanical, and electrical properties are studied. XRD and SEM show that graphene nanosheets are well dispersed in the PTT matrix without forming crystalline aggregates even at high EG content. Thermal stability and dynamic mechanical moduli of the nanocomposites are substantially improved by EG addition, and a pronounced increase in electrical volume resistivity from an insulator to almost a semiconductor is observed with increasing EG content. The electrical percolation threshold of the nanocomposites is found to be formed at the EG concentration between 3.0 and 5.0 wt.‐%.
PCL‐based nanoclay (layered silicate) nanocomposites are prepared using a small scale intermeshing co‐rotating twin‐screw extruder. Improving the level of nanoclay dispersion in PCL nanocomposites is obtained by changing the extrusion parameters. Increasing the screw speed and decreasing the throughput leads to an improved dispersion quality, as observed from the improved mechanical properties of the nanocomposites as well as from their clearly affected rheological and crystallization behavior. Furthermore, a commercially available software that simulates the twin‐screw extrusion process (LUDOVIC) is used to asses the processing parameters applied for making the nanocomposites.
It is demonstrated that SNN‐assisted melt dispersion can lead to a significant improvement of the thermal conductivity of PC/MWCNT composites accompanied by a dramatic reduction in their linear CTE. The thermal conductivity of the SNN‐containing composites after the 2‐step process was about 95% higher than that of neat PC and 25% higher than that from 1‐step processing at same loading. The CTE below the glass‐transition temperature of composites with a 1.0 wt.‐% MWCNT loading is substantially reduced compared to the neat polymer. A reduction in the CTE of up to 60.8% is observed for composites from the 2‐step process. Simultaneous achievement of high thermal conductivity and low CTE is required for electronic packaging in microelectronics for device protection.
Copolymers of 3,4‐ethylenedioxythiophene and 3‐methylthiophene have been prepared by recurrent potential pulses using monomer mixtures with various concentration ratios, their properties being compared with those of the corresponding homopolymers. In addition, different technological applications have been tested for the generated copolymers. Results indicate that the properties of the copolymers are closer to those of poly(3,4‐ethylenedioxythiophene) than to those poly(3‐methylthiophene). Furthermore, the ability of the copolymers to store charge and to interact with plasmid DNA suggest that they are very promising materials.
The influence of the thermal history experienced during injection molding on the mechanical properties of polycarbonate is investigated. Distributions of the yield stress as they result from inhomogeneous cooling during processing, predicted by a previously developed modeling approach, are validated and are in good agreement with experiment. Predictions of the mechanical performance for different mold temperatures during processing are also validated over a range of applied strain and deformation rates and applied stresses and forces, for simple tensile bars and an actual product. Good agreement is found. It is shown that mold temperature has a tremendous influence on the life time of polymer products, which can differ by more than two orders of magnitude.
PA nanocomposites are prepared from clays organophilized with a phosphonium and an ammonium salt, and sodium montmorillonite is used as reference. The analysis of mechanical and micromechanical properties of the composites reveal that several micromechanical deformation processes occur in the PA/MMT composites. The matrix cavitates at relatively small stress. Processes related to non‐exfoliated clay structural units are initiated at larger stresses. Sound is emitted mainly by the fracture of particles, but debonding may also occur. The plastic deformation of the matrix dominates at larger stresses and deformations. The various local deformations are independent of each other and composite properties are not determined by silicate related processes but by the deformation of the matrix.
