Improving the mechanical properties of thermoplastic starch/poly(vinyl alcohol)/clay nanocomposites

Thermoplastic starch/poly(vinyl alcohol) (PVOH)/clay nanocomposites, exhibiting the intercalated and exfoliated structures, were prepared via melt extrusion method. The effects of clay cation, water, PVOH and clay contents on clay intercalation and mechanical properties of nanocomposites were investigated. The experiments were carried out according to the Taguchi experimental design method. Montmorillonite (MMT) with three types of cation or modifier (Na⁺, alkyl ammonium ion, and citric acid) was examined. The prepared nanocomposites with modified montmorillonite indicated a mechanical improvement in the properties in comparison with pristine MMT. It was also observed that increases in tensile strength and modulus would be attained for nanocomposite samples with 10%, 5% and 4% (by weight) of water, PVOH and clay loading, respectively. The clay intercalation was examined by X-ray diffraction (XRD) patterns. The chemical structure and morphology of the optimum sample was also probed by FTIR spectroscopy and transmission electron microscopy (TEM).     

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.     

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.     

A comparative study of the electrical and mechanical properties of epoxy nanocomposites reinforced by CVD- and arc-grown multi-wall carbon nanotubes

In this study, three different types of multi-wall carbon nanotubes (MWCNTs) were compared as nanostructured reinforcements in epoxy polymers: commercially available CVD-MWCNTs, synthesised in an industrial process, aligned-CVD-MWCNTs and arc-grown MWCNTs, both obtained from a lab-scale processes. The nanocomposite properties were characterised by means of electron microscopy, rheological, electrical and mechanical methods. Industrial CVD-MWCNTs are favourable for the implication of an electrical conductivity in the epoxy due to their high tendency to form conducting networks. The less entangled structure of aligned-CVD-MWCNTs turns out to be favourable for an easy dispersion and low viscosity in epoxy at similar conductivities compared to the CVD-MWCNTs. Additionally, they provide the highest increase in fracture toughness (∼17%). Arc-grown MWCNTs do not offer any electrical conductivity in epoxy without sufficient purification methods. Their high level of impurities and short length further complicate the transfer of their good electrical and mechanical properties into the nanocomposite.     

Dielectric properties of montmorillonite clay filled poly(vinyl alcohol)/poly(ethylene oxide) blend nanocomposites

Organic–inorganic nanocomposites of poly(vinyl alcohol) (PVA)–poly(ethylene oxide) (PEO) blend filled with montmorillonite (MMT) nanoclay up to 10 wt.% concentration were synthesized by aqueous solution-cast technique. The complex dielectric function, electrical conductivity, electric modulus and impedance spectra of the nanocomposites were measured in the frequency range 20 Hz–1 MHz at ambient temperature. A direct correlation was observed between the real part of dielectric function and the mean relaxation time of the polymer chain segmental dynamics, with the exfoliated and intercalated MMT clay structures, and the extent of miscibility between PVA and PEO due to hydrogen bonded bridging through exfoliated MMT clay nanosheets. The large increase of dielectric relaxation time revealed that the dispersed exfoliated nanoscale MMT clay in the polymers blend matrix produces a large hindrance to the polymer chain dynamics. Results confirm that the real part of dielectric function of the nanocomposites can be tailored by varying amount of MMT clay filler for their use as nanodielectric materials in the microelectronic technology.     

Preparation and mechanical characterization of laser ablated single-walled carbon-nanotubes/polyurethane nanocomposite microbeams

We report on the preparation of nanocomposites consisting of laser synthesized single-walled carbon nanotubes (C-SWNTs) reinforcing a polyurethane. Prior to their incorporation into the polymer matrix, the C-SWNTs were purified, and characterized by means of various techniques. The purification in nitric acid added carboxylic groups to the C-SWNTs. A procedure to properly disperse the nanomaterials in the polymer was developed involving high shear mixing using a three-roll mill and a non-covalent functionalization of the nanotubes by zinc protoporphyrin IX molecule. The incorporation of the C-SWNTs into the resin led to an increase of the viscosity and the apparition of a slight shear-thinning behavior. A further increase of the shear-thinning behavior using fumed silica particles enabled the direct-write fabrication of microbeams. Mechanical characterization revealed significant increase in both strength (by ∼64%) and modulus (by more than 15 times). These mechanical enhancements are believed to be a consequence of the successful covalent and the non-covalent functionalizations of the nanotubes.     

Experimental and theoretical analyses of mechanical properties of PP/PLA/clay nanocomposites

Compatibilized and non-compatibilized blends of polypropylene (PP) and poly(lactic acid) (PLA) with various compositions containing nanoclay particles were prepared by one step melt compounding in a twin screw extruder. Two nanocomposite systems with different matrices i.e. PP-rich (75/25 composition) containing Cloisite 15A and PLA-rich (25/75 composition) containing Cloisite 30B were selected for investigation of effect of nanoclays and n-butyl acrylate glycidyl methacrylate ethylene terpolymers (PTW) as compatibilizer on mechanical properties of PP/PLA/clay nanocomposites. Tensile and impact properties of the nanocomposite systems were investigated and correlated with their microstructures. Tensile modulus and strength of the blends were increased while elongation at break decreased by increasing PLA content. There was an irregular relationship between impact strength of the blends and PLA content. Several proposed models for blends and nanocomposites were used for prediction of tensile modulus of the samples. Most of the proposed models for blends could predict the tensile modulus of the blends successfully at low content of PLA. Another notable point was that most of the micromechanical models for nanocomposites fitted well to experimental values at low content of the clays and showed deviations at high clay loadings.     

Effect of carbon nanofibers (CNFs) content on thermal and mechanical properties of CNFs/SiC nanocomposites

Carbon nanofibers dispersed β-SiC (CNFs/SiC) nanocomposites were prepared by hot-pressing via a transient eutectic phase route at 1900 °C for 1 h under 20 MPa in Ar. The effects of additional CNFs content between 1 and 10 wt.% were investigated, based on densification, microstructure, thermal and mechanical properties. The CNFs/SiC nanocomposites by the CNFs contents below 5 wt.% exhibited excellent relative densities over 98% with well dispersed CNFs. However, the CNFs/SiC nanocomposites containing the CNFs of 10 wt.% possessed a relative density of 92%, accompanying CNFs agglomerates and many pores located inside the agglomerates. The three point bending strength gradually decreased with the increase of CNFs content, but the indentation fracture toughness increased to 5.7 MPa m^1/2 by the CNFs content of 5 wt.%. The thermal conductivity was enchanced with the increase of CNFs content and represented a maximum value of 80 W/mK at the CNFs content of 5 wt.%.     

Effect of nanotube geometry on the elastic properties of nanocomposites

Many analytical models replace carbon nanotubes with “effective fibers” to bridge the gap between the nano and micro-scales and allow for the calculation of the elastic properties of nanocomposites using micromechanics. Although curvature of nanotubes can have a direct impact on these properties, it is typically ignored. In this work, the nanotube geometry in 3D is included in the calculation of the elastic properties of a modified effective fiber. The strain energy of the nanotube and the effective fiber are calculated using Castligiano’s theorem and constraints imposed by the matrix on the deformation are taken into consideration. Model results are compared to results from archived literature, and a reasonable agreement is observed. Results show that the effect of nanotube curvature on reducing the modulus of the effective fiber is not limited to in-plane curvature but also to curvature in 3D. The impact of the nanotube curvature on the elastic properties of nanocomposites is studied utilizing the modified fiber model and the approach developed by Mori–Tanaka. Analytical results show that for a low weight fraction of nanotubes the effect of curvature seems to be minor and as the weight fraction increases, the effect of nanotube curvature becomes critical.     

Preparation and properties of poly (p-phenylene sulfide)/multiwall carbon nanotube composites obtained by melt compounding

In this paper, electrical and mechanical properties of Poly (p-phenylene sulfide) (PPS)/multi-wall carbon nanotubes (MWNTs) nanocomposites were reported. The composites were obtained just by simply melt mixing PPS with raw MWNTs without any pre-treatment. The dispersion of MWNTs and interfacial interaction were investigated through SEM &TEM and Raman spectra. The rheological test and crystallization behavior were also investigated to study the effects of MWNTs concentration on the structure and chain mobility of the prepared composites. Though raw MWNTs without any pre-treatment were used, a good dispersion and interaction between PPS and MWNTs have been evidenced, resulting in a great improvement of electrical properties and mechanical properties of the composites. Raman spectra showed a remarkable decrease of G band intensity and a shift of D bond, demonstrating a strong filler–matrix interaction, which was considered as due to π–π stacking between PPS and MWNTs. The storage modulus (G′) versus frequency curve presented a plateau above the percolation threshold of about 2–3 wt% with the formation of an interconnected nanotube structure, indicative of ‘pseudo-solid-like’ behavior. Meanwhile, a conductive percolation threshold of 5 wt% was achieved and the conductivity of nanocomposites increased sharply by several orders of magnitude. The difference between electrical and rheological percolation threshold, and the effect of critical percolation on the chain mobility, especially on crystallization behavior of PPS, were discussed. In summary, our work provides a simple and fast way to prepare PPS/MWNTs nanocomposites with good dispersion and improved properties.     

Effect of shearing on the orientation, crystallization and mechanical properties of HDPE/attapulgite nanocomposites

High density polyethylene (HDPE)/attapulgite (AT) nanocomposites, prepared by conventional injection molding (CIM) and dynamic packing injection molding (DPIM), were investigated with focus on AT-induced crystallization and orientation under shear. Infrared spectroscopy (FTIR) analysis showed there is no special chemical interaction between HDPE and AT, but shear induced significant changes on the material structure and properties. Differential scanning calorimetry (DSC) analysis showed strong nucleation effect by AT especially under shear. And more, shear will induce much better dispersion of AT in the DPIM sample vs. CIM. AT nanorods and lamellae of HDPE are more organized in the DPIM sample while there is only random distribution in the CIM sample. Most AT nanorods embed in the HDPE lamellae and form a brush-like hybrid structure due to shear. The shear-induced orientation will be enhanced with higher AT loading. The mechanical performance of the composites was significantly improved via DPIM.     

Mechanical and microstructural properties of Nylon-12/carbon black composites: Selective laser sintering versus melt compounding and injection molding

Composites of Nylon-12 reinforced with 4 wt.% carbon black (CB) manufactured by selective laser sintering (SLS) are compared in terms of flexural strength and flexural modulus, tensile strength and tensile modulus, and impact strength to composites made by extrusion and injection molding (Ex-IM). The Nylon-12 system made by SLS had 25% and 35% higher flexural and tensile modulus, respectively, compared to the Nylon-12 system made by Ex-IM and ∼10% higher strength. However, upon addition of CB both the modulus and the strength of the composites made by SLS were significantly lower compared to composites made by Ex-IM. This is due to the poor dispersion of nanoscale CB and due to the higher porosity of the composites made by SLS, which also explains the relatively low impact strength observed. Based on XRD and DSC studies, it is concluded that the composites made by the two processing methods did not differ significantly in their crystallization characteristics such as the degree of crystallinity, crystal type, and lamellar thickness. However, it was found that CB acted as a nucleating agent for Nylon-12 when Ex-IM was used, leading thus to smaller but more numerous polymer crystals.     

Effect of carbon nanotube (CNT) content on the mechanical properties of CNT-reinforced aluminium composites

The interest in carbon nanotubes (CNTs) as reinforcements for aluminium (Al) has been growing considerably. Efforts have been largely focused on investigating their contribution to the enhancement of the mechanical performance of the composites. The uniform dispersion of CNTs in the Al matrix has been identified as being critical to the pursuit of enhanced properties. Ball milling as a mechanical dispersion technique has proved its potential. In this work, we use ball milling to disperse up to 5 wt.% CNT in an Al matrix. The effect of CNT content on the mechanical properties of the composites was investigated. Cold compaction and hot extrusion were used to consolidate the ball-milled Al–CNT mixtures. Enhancements of up to 50% in tensile strength and 23% in stiffness compared to pure aluminium were observed. Some carbide formation was observed in the composite containing 5 wt.% CNT. In spite of the observed overall reinforcing effect, the large aspect ratio CNTs used in the present study were difficult to disperse at CNT wt.% greater than 2, and thus the expected improvements in mechanical properties with increase in CNT weight content were not fully realized.     

The effects of Clay on fire performance and thermal mechanical properties of woven glass fibre reinforced polyamide 6 nanocomposites

The effects of small amount of organically modified Clay (Clay) in polyamide 6 (PA6) on fire performance and thermal mechanical properties of Clay/PA6/woven glass fibres (GF) laminates are investigated by cone calorimeter test, dynamic mechanical thermal analysis (DMTA), and heat distort temperature (HDT) measurement. The mechanical properties, such as tensile and flexural properties of Clay/PA6 composites and Clay/PA6/GF laminates were also measured. Up to 3 wt.% Clay in a Clay/PA6/GF laminate with fibre volume fraction of 30 vol.% delayed the ignition time and peak heat release rate (PHRR) time by 55% and 118%, respectively, even though the value of the PHRR or the HDT was not significantly affected. 2 wt.% Clay increased flexural modulus and strength of the Clay/PA6/GF laminate by 10% and 16%, respectively, but more Clay did not increase the mechanical properties accordingly. Small amount of Clay does not affect glass fibre dominated properties, such as HDT, but do affect matrix dominated properties, and significantly affect the fire performance in terms of delaying ignition time and PHRR time. Optimization of laminate making process could benefit from additions of more Clay, therefore further improve fire performance and enhance mechanical properties.     

Effect of mechanical activation pretreatment on the properties of sugarcane bagasse/poly(vinyl chloride) composites

This current work is concerned with the pretreatment of sugarcane bagasse (SCB) by mechanical activation (MA) using a self-designed stirring ball mill and surface modification of SCB using aluminate coupling agent (ACA). The untreated and differently treated SCBs were used to produce composites with poly(vinyl chloride) (PVC) as polymer matrix. The activation grade (A_g) measurement and Fourier transform infrared (FTIR) analysis of SCB showed that MA enhanced the condensation reaction between ACA and hydroxyl groups of the SCB fibres, which obviously increased the hydrophobicity of SCB. It was found that the mechanical properties of both the PVC composites reinforced by SCB with and without ACA modification increased with increasing milling time (t_M). Scanning electron microscopy (SEM) analysis showed that MA pretreatment significantly improved the dispersion of SCB in the composites and interfacial adhesion between SCB and PVC matrix, resulting in better mechanical properties of the composites.     

Highly conductive graphene oxide/polyaniline hybrid polymer nanocomposites with simultaneously improved mechanical properties

Graphene oxide (GO) was added to a polymer composites system consisting of surfactant-wrapped/doped polyaniline (PANI) and divinylbenzene (DVB). The nanocomposites were fabricated by a simple blending, ultrasonic dispersion and curing process. The new composites show higher conductivity (0.02–9.8 S/cm) than the other reported polymer system filled with PANI (10⁻⁹–10⁻¹ S/cm). With only 0.45 wt% loading of GO, at least 29% enhancement in electric conductivity and 29.8% increase in bending modulus of the composites were gained. Besides, thermal stability of the composites was also improved. UV–Vis spectroscopy, X-ray diffraction analysis (XRD) and scanning electron microscopy (SEM) revealed that addition of GO improves the dispersion of PANI in the polymer composite, which is the key to realize high conductivity.     

PHBV nanocomposites based on organomodified montmorillonite and halloysite: The effect of clay type on the morphology and thermal and mechanical properties

The aim of this study was to evaluate the effect of the addition of two types of nanoparticles, organomodified montmorillonite Cloisite® 30B (C-30B), and a tubular like clay, halloysite (HNT), on the morphology and thermal and mechanical properties of poly(hydroxybutyrate-co-hydroxyvalerate) – PHBV nanocomposites. TEM and WAXD results showed a combination of a few tactoids and a partially exfoliated structure for PHBV/C-30B nanocomposites and a good dispersion of HNT in the PHBV matrix. DSC analysis indicated a lower nucleation density with the addition of nanoparticles. Furthermore, the presence of C-30B led to the formation of double melting peaks, related to different crystalline phases. However, a higher melting temperature was obtained for PHBV/HNT nanocomposites. A general increase in the Young’s modulus was observed. However, for PHBV/C-30B nanocomposites, this enhancement was at the expense of the strain at break and impact strength, probably due to the degradation of the polymer during processing.     

PLA/algae composites: Morphology and mechanical properties

Bio-composites with poly(lactic) acid as matrix and various algae (red, brown and green) as filler were prepared via melt mixing. Algae initial size (below 50 μm and between 200 and 400 μm) and concentration (from 2 to 40 wt%) were varied. First, algae morphology, composition and surface properties are analysed for each algae type. Second, an example of algae particle size decrease during processing is given. Finally, tensile properties of composites are analysed. The surface of algae flakes was covered with inorganic salts affecting filler–matrix interactions. The Young’s modulus of composites increased at 40 wt% load of algae as compared with neat PLA although the strain at break and tensile strength decreased. In most cases the influence of algae type was minor. Larger flakes led to better mechanical properties compared to the smaller ones.