Fabrication and characterization of transparent ZnO–SiO2/silicone nanocomposites with tunable emission colors

ZnO quantum dot-SiO₂ (Z–S) nanocomposite particles with tunable photoluminescence were obtained via hydrolyzing tetraethoxysilane in the ZnO quantum dots containing ethanol solution with further calcinations. The nanocomposite particles were introduced into a transparent silicone matrix and the ratio of ZnO to SiO₂ was adjusted to maintain the transmittance in terms of the filler-matrix refractive index matching principle. Finally, transparent Z–S/silicone nanocomposites with tunable emission colors were successfully fabricated which may find potential applications as encapsulating materials for highly bright LED lamps.     

Electrical properties of polyvinylidene fluoride (PVDF)/multi-walled carbon nanotube (MWCNT) semi-transparent composites: Modelling of DC conductivity

Transparent conductive composites can be achieved from PVDF–MWCNT at very low concentration of MWCNT. These composites show different degree of UV–Visible radiation absorption depending on MWCNT concentration in composites. The composition dependent dielectric properties and AC conductivity were also measured for these composites. Properties like AC conductivity, dielectric constant and loss are increasing with filler concentration. The variations of DC conductivity against composition and temperature are also reported. The electrical hysteresis and electrical set are observed for PVDF–MWCNT composites when subjected to heating–cooling cycle. The validity of different theoretical models depicting percolation threshold with respect to DC conductivity was tested for these composites.     

High performance polyurethane/functionalized graphene nanocomposites with improved mechanical and thermal properties

This communication reported the substantial improvement in the mechanical and thermal properties of a polyurethane (PU) resulting from the incorporation of well-dispersed graphene oxide (GO). The stress transfer benefited from the covalent interface formed between the PU and GO. The Young’s modulus of the PU was improved by ∼7 times with the incorporation of 4 wt% GO, and the improvement of ∼50% in toughness was achieved at 1 wt% loading of GO without losing elasticity. Significant improvements were also demonstrated in the hardness and scratch resistance measured by nano-indentation. Thermogravimetric analysis revealed that the decomposition temperature was increased by ∼50 °C with the addition of 4 wt% GO.     

Polylactide (PLA)-clay nanocomposites prepared by melt compounding in the presence of a chain extender

Polylactide-layered silicate nanocomposites with and without a chain extender were prepared by melt mixing using a twin-screw extruder. An organo-modified clay, Cloisite® 30B, and a chain extender Joncryl®-ADR 4368F were employed in this study. The effect of the chain extender and processing conditions on the properties of the PLA-clay nanocomposites were investigated for different strategies of mixing. The resulting nanocomposites were characterized by X-ray diffraction (XRD), while their morphology was observed by SEM and TEM. The incorporation of the chain extender could enhance the degree of clay dispersion provided that it is judiciously added to the nanocomposite. The corresponding results revealed that the Joncryl-based nanocomposites, where nanoclay platelets were well-dispersed, exhibited a significantly reduced permeability as compared to others. The mechanical properties of the neat PLA, the PLA and Joncryl-based nanocomposites were also examined. The increased molecular weight in Joncryl-based nanocomposites caused a significant increase in the modulus, drawability and toughness of the samples.     

Influence of different carbon nanotubes on the electrical and mechanical properties of melt mixed poly(ether sulfone)-multi walled carbon nanotube composites

Commercial Udel® poly(ether sulfone) (PSU) was filled with three different commercially available multiwalled carbon nanotubes (MWCNTs) by small scale melt mixing. The MWCNTs were as grown NC 7000 and two of its derivatives prepared by ball milling treatment. One of them was unmodified (NC 3150); the other was amino modified (NC 3152). The main difference beside the reactivity was the reduced aspect ratio of NC 3150 and NC 3152 caused by ball milling process. All PSU/MWCNT composites with similar filler content were prepared under fixed processing conditions and comparative analysis of their electrical and mechanical properties were performed and were correlated with their microstructure, characterized by optical microscopy, scanning electron microscopy (SEM), and transmission electron microscopy (TEM). A non-uniform MWCNT dispersion was observed in all composites. The MWCNTs were present in form of agglomerates in the size of 10–60 μm whereas the deagglomerated part was homogeneously distributed in the PSU matrix. The differences in the agglomeration states correlate with the variations of properties between different PSU/MWCNT composites. The lowest electrical percolation threshold of 0.25–0.5 wt.% was observed for the shortened non-functionalized MWCNT composites and the highest for amine-modified MWCNT composites (ca. 1.5 wt.%). The tensile behavior of the three composites was only slightly altered with CNT loading as compared to the pure PSU. However, the elongation at break showed a reduction with MWCNT loading and the reduction was least for composite with best MWCNT dispersion.     

Morphology, mechanical and thermal properties of graphene-reinforced poly(butylene succinate) nanocomposites

Graphene nanosheets (GNSs) reinforced poly(butylene succinate) (PBS) nanocomposites are facilely obtained by a solution-based processing method. Graphene nanosheets, which are derived from chemically reduced graphite oxide (GO), are characterized by AFM, TEM, XRD and Raman spectra. The state of dispersion of the GNSs in the PBS matrix is examined by SEM observations that reveals homogeneous distribution of GNSs in PBS matrix. A 21% increase in tensile strength and a 24% improvement of storage modulus are achieved by addition of 2.0 wt% of GNS. The electrical conductivity and thermal stability of the graphene-based nanocomposite are also improved. DSC measurement indicates that the presence of graphene sheets does not have a remarkable impact on the crystallinity of the nanocomposites. Therefore, the high performances of the nanocomposites are mainly attributed to the uniform dispersion of GNSs in the polymer matrix and strong interfacial interactions between both components.     

The effect of alkaline and silane treatments on mechanical properties and breakage of sisal fibers and poly(lactic acid)/sisal fiber composites

The main goals of this work were to study the effect of different chemical treatments on sisal fiber bundles tensile properties as well as on tensile properties of composites based on poly(lactic acid) (PLA) matrix and sisal fibers. For this purpose, sisal fibers were treated with different chemical treatments. After treating sisal fibers the tensile strength values decreased respect to untreated fiber ones, especially when the combination of NaOH + silane treatment was used. Taking into account fiber tensile properties and fiber/PLA adhesion values, composites based on silane treated fibers would show the highest tensile strength value. However, composites based on alkali treated and NaOH + silane treated fibers showed the highest tensile strength values. Finally, experimental tensile strength values of composites were compared with those values obtained using micromechanical models.     

Synthesis and properties of poly(hexamethylene terephthalate)/multiwall carbon nanotubes nanocomposites

Poly(hexamethylene terephthalate) (PHT)/carbon nanotubes (CNT) nanocomposites containing 1% and 3% (w/w) of filler were prepared by two procedures: in situ ring-opening polymerization of hexamethylene terephthalate cyclic oligomers in the presence of CNT and melt blending of PHT/CNT mixtures. Arc discharge multiwalled carbon nanotubes, both pristine (MWCNT) and hydroxyl functionalized (MWCNT-OH), were used. The objective was to evaluate the effect of preparation procedure, nanotube side-wall functionalization and amount of nanotube loaded on properties of PHT. All nanocomposites showed an efficient distribution of the carbon nanotubes within the PHT matrix but interfacial adhesion and reinforcement effect was dependent on both functionalization and nanotubes loading. Significant differences in thermal stability and mechanical properties ascribable to functionalization and processing were observed among the prepared nanocomposites. All the prepared nanocomposites showed enhanced crystallizability due to CNT nucleating effects although changes in melting and glass transition temperatures were not significant.     

Utilization of polymer degradation to modify electrical properties of poly(l-lactide)/poly(methyl methacrylate)/carbon filler composites

This research attempts to utilize polymer degradability in modifying electrical properties of poly(l-lactide) (PLLA)/poly(methyl methacrylate) (PMMA)/carbon fillers composites. Three kinds of carbon particles, i.e. carbon black, vapor-grown carbon fiber, and carbon nanotube, were compounded with PLLA/PMMA blend, followed by hydrolytic degradation of the composites, resulted in degradation of PLLA molecular chain from the surface of samples, with PMMA and carbon particles remained undegraded. By controlling degradation rate, it was possible to prepare samples with low surface resistivity, yet at the same time exhibited high value of volume resistivity. It was also found that final electrical properties of degraded composites depend on the size and the shape of the fillers.     

Liquid sensing properties of fibres prepared by melt spinning from poly(lactic acid) containing multi-walled carbon nanotubes

Poly(lactic acid) (PLA)/multi-walled carbon nanotube (MWNT) composites were melt spun with different take-up velocities (max. 100 m/min) to obtain electrically conductive fibres. The incorporation of MWNT contents between 0.5 and 5.0 wt.% was realised in a previous melt mixing process using twin-screw extrusion. The relative resistance change of the fibres caused by contact with different solvents (water, n-hexane, ethanol, methanol) and solvent concentrations was used as liquid sensing response, whereas the time dependent resistance was recorded during immersion and drying cycles. Transmission electron microscopy and Raman spectroscopy indicated enhanced orientation of MWNT along the fibre axis with take-up velocity, resulting in decreased sensitivity during solvent contact. Additionally, sensitivity decreased as the weight content of MWNT increased and was furthermore dependent on the characteristics of used solvents. In context with the targeted application of leakage detection, fibres with low MWNT amount and low draw down ratio (as extruded fibres with 2 wt.% MWNT) are suitable, as they showed relative resistance changes of up to 87% after 10 min immersion in methanol even if the recovery upon drying was suppressed significantly.     

Filling behavior,morphology evolution and crystallization behavior of microinjection molded poly(lactic acid)/hydroxyapatite nanocomposites

In this paper, the filling behavior, morphology evolution, crystallization behavior, thermal stability and mechanical property of poly(lactic acid) (PLA)/hydroxyapatite (HA) nanocomposite under microinjection molding conditions were systematically investigated. The comparison between micropart and macropart of PLA/HA nanocomposite was also conducted. Results showed that in the four stages occurring in the microinjection molding process, the mold cavity filling stage is an extremely rapid process and injection speed influences the filling behavior much more significantly than mold temperature. The remarkably enhanced shear force field generated under microinjection molding conditions proves to be beneficial to formation of highly oriented PLA matrix self-fibrillating structure, improvement of HA filler dispersion and enhancement of interfacial combination. Formation of such a highly oriented structure could lead to the remarkable difference in both crystallization behavior and mechanical property between micropart and macropart. The PLA/HA nanocomposite micropart possessed a significantly enhanced mechanical property and showed a good application prospect.     

Preparation,structure and thermal properties of polylactide/sepiolite nanocomposites with and without organic modifiers

Polylactide-based nanocomposites containing unmodified and organic modified sepiolite were prepared through a solution casting method. The structure and properties of materials were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM) and thermogravimetric analysis (TGA). From the results it can be concluded that the bundles of sepiolite have been dispersed into small aggregates containing several nanorods without destroying the crystal structure. Sepiolite nanofibers were well dispersed in the PLA matrix, exhibiting a randomly orientation with the contact among them in all cases. But the thermal stability of nanocomposites has been improved more by introducing unmodified sepiolite than that with organic modified sepiolite, which has also been confirmed by molecular dynamics simulation results that hydrophobic parts of organic modifiers could prevent the interaction between PLA molecules and sepiolite surface.     

In vitro degradation of porous poly(lactic acid)/quantum dots scaffolds

In this study, cadmium selenide/zinc sulfide (CdSe/ZnS) quantum dots (QDs) were introduced into poly(lactic acid) (PLA) for fabrication of photoluminescent PLA/QDs scaffolds. TEM images revealed that the QDs were uniformly dispersed in the PLA. Compressive modulus and thermal stability of the PLA/QDs scaffolds are higher than those of the unfilled PLA scaffold. Cytotoxicity test results confirmed the non-cytotoxicity of the PLA/QDs scaffolds. During the process of in vitro degradation, the degradation rate of the PLA was accelerated by the presence of the QDs, and the molecular weight distributions of the PLA/QDs scaffolds were much broader when compared with the unfilled PLA ones. During the first 84 weeks of the degradation process, the photoluminescence (PL) intensity of the PLA/QDs scaffolds decreased with almost the same degradation ratio. The results suggested that the CdSe/ZnS QDs have potential applications for monitoring in vivo degradation of tissue engineering scaffolds.     

Influence of electrolessly silver-plated multi-walled carbon nanotubes on thermal conductivity of epoxy matrix nanocomposites

In this work, multi-walled carbon nanotubes (MWCNTs) were electrolessly Ag-plated in order to investigate the effect of plating time on the thermal conductivity of Ag-plated MWCNTs-reinforced epoxy matrix composites. MWCNT surfaces were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS). The thermal conductivity of Ag-plated MWCNT-reinforced epoxy nanocomposites was measured using the thermal equilibrium method with ASTM D5470. From the results, it was found that the thermal conductivity of the composites enhanced with increasing plating time. In particular the Ag-10/EP sample showed more than 150% enhancement of the thermal conductivity compared to the as-received CNTs/EP sample. These results were attributed to the high contents of Ag particles and the increase of the interfacial adhesion between the Ag-CNTs and EP matrix in the composites.     

The effect of pre-softened wood chips on wood fibre aspect ratio and mechanical properties of wood–polymer composites

The objective of this work was to study the effect of chemical pre-treatment and moisture content of wood chips on the wood particle aspect ratio after compounding in a twin-screw extruder and on the mechanical properties of wood–polymer composites (WPCs). Composites with 50 wt.% wood content were manufactured using pre-treated and untreated wood chips. The effect of wood moisture content on composite properties was studied by using dried and undried wood chips. The mechanical properties and fracture surfaces of the composites as well as the microstructure and aspect ratio of wood particles after compounding were studied. The highest wood particle aspect ratio after extrusion was achieved by using pre-treated, undried wood chips as raw material. The chemical pre-treatment was found to enhance the defibration of wood chips as well as the mechanical properties of the composites.     

Enhancement of tensile and thermal properties of epoxy nanocomposites through chemical hybridization of carbon nanotubes and alumina

This paper presents the properties of epoxy nanocomposites, prepared using a synthesized hybrid carbon nanotube–alumina (CNT–Al₂O₃) filler, via chemical vapour deposition and a physically mixed CNT–Al₂O₃ filler, at various filler loadings (i.e., 1–5%). The tensile and thermal properties of both nanocomposites were investigated at different weight percentages of filler loading. The CNT–Al₂O₃ hybrid epoxy composites showed higher tensile and thermal properties than the CNT–Al₂O₃ physically mixed epoxy composites. This increase was associated with the homogenous dispersion of CNT–Al₂O₃ particle filler; as observed under a field emission scanning electron microscope. It was demonstrated that the CNT–Al₂O₃ hybrid epoxy composites are capable of increasing tensile strength by up to 30%, giving a tensile modulus of 39%, thermal conductivity of 20%, and a glass transition temperature value of 25%, when compared to a neat epoxy composite.     

Morphology and degradation properties of PCL/HYAFF11® composite scaffolds with multi-scale degradation rate

The analysis of scaffold degradation is a promising strategy for understanding the dynamic changes in texture and pore morphology which accompany polymer resorption, and for collecting same fundamental indicators regarding the potential fate of the scaffold in the biological environment. In this study, we investigate the morphology and degradation properties of three composite scaffolds based on poly(ε-caprolactone) (PCL) embedded with benzyl ester of hyaluronic acid (HYAFF11®) phases, and, in turn, different reinforcement systems – i.e., calcium phosphate particles or continuous poly(lactic acid) (PLA) fibres. Scanning electron microscopy (SEM) and μ-tomography supported by digital image analysis enabled a not invasive investigation of the scaffold morphology, providing a quantitative assessment of porosity (which ranged from 63.1 to 82.8), pore sizes (which varied from 170.5 to 230.4 μm) and pore interconnectivity. Thermal analyses (DSC and TGA) and Raman spectroscopy demonstrated the multi-scale degradation of the composite with highly tailoring degradation kinetics depending on the component material phases and scaffold architecture changes, due to their conditioning in simulated in vivo environment (i.e., SBF solution). These results demonstrate that the judicious mixing of materials with faster (i.e., HYAFF11) and slower (i.e., PLA and PCL) degradation kinetics, different size and shape (i.e., domains, particles or long fibres), certainly concurs to design a smart composite scaffold with time-controlled degradation which can support the regeneration of a large variety of tissues, from the cartilage to the bone.     

Processing and mechanical properties evaluation of glass fiber-reinforced PTFE laminates

A specific manufacturing process to obtain continuous glass fiber-reinforced PTFE laminates was studied and some of their mechanical properties were evaluated. Young’s modulus and maximum strength were measured by three-point bending test and tensile test using the Digital Image Correlation (DIC) technique. Adhesion tests, thermal analysis and microscopy were used to evaluate the fiber–matrix adhesion, which is very dependent on the sintering time. The composite material obtained had a Young’s modulus of 14.2 GPa and ultimate strength of 165 MPa, which corresponds to approximately 24 times the modulus and six times the ultimate strength of pure PTFE. These results show that the PTFE composite, manufactured under specific conditions, has great potential to provide structural parts with a performance suitable for application in structural components.     

Crystallization,mechanical performance and hydrolytic degradation of poly(butylene succinate)/graphene oxide nanocomposites obtained via in situ polymerization

Poly(butylene succinate) (PBS)/graphene oxide (GO) nanocomposites were fabricated via in situ polymerization with very low GO content (from 0.03 to 0.5 wt%). The microstructures of the nanocomposites were characterized with Raman spectroscopy, fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), sedimentation experiments and atomic force microscopy (AFM). The results showed that PBS chains have been successfully grafted onto GO sheets during in-situ polymerization, accompanied by the thermo-reduction from GO to graphene. The grafted GO displayed a great nucleating effect on PBS crystallization, resulting in largely improved crystallization temperature and decreased spherules size. A simultaneous enhancement in tensile strength and elongation was achieved for PBS/GO nanocomposites fiber. Meanwhile, increase in hydrolytic degradation rate was also observed for these nanohybrids. Our result indicates that using very low content GO is a simple way to achieve good dispersion yet with remarkable property enhancement for polymer/GO nanocomposites.     

In situ preparation of reinforced polyimide nanocomposites with the noncovalently dispersed and matrix compatible MWCNTs

High performance MWCNT-reinforced polyimide nanocomposites were prepared through in situ polymerization route. 2,6-Diaminoanthraquinone (2,6-DAAQ) was selected to serve as both a diamine comonomer, and a noncovalent dispersant of MWCNTs through π–π interaction. The good dispersion of MWCNTs in both solution and polymer matrix, and high compatibility derived from the structural similarity have been proved to be particularly advantageous for the interfacial adhesion and load transfer from the polymer matrix to MWCNTs. The nanocomposites with 0.50–0.75 wt% MWCNTs had the most excellent thermal stability, thermomechanical and tensile properties, and the electrical conductivity also achieved a sharp increase at such low content. The load transfer efficiency was calculated based on both theoretical model and microscopical size measurement, and the results were rather reasonable within accepted error range.