Low density polyethylene – Chitosan composites

With the aim of develop new materials for active food packaging, composites of low-density polyethylene (LDPE) with chitosan (CS) or chitosan sodium montmorillonite clay nanocomposites (CSnano), with or without Irganox 1076 commercial synthetic antioxidant or vitamin E (VE) as natural antioxidant were prepared by melt processing. The obtained materials have been characterized by processing behavior, mechanical and thermal properties, positive groups determination, atomic force microscopy and standard tests to assess antimicrobial and antioxidant activities. The compositions assuring insignificant decrease in mechanical and thermal properties were selected as LDPE/3CSnano/VE and LDPE/6CSnano/VE. It has been shown the chitosan imparts antimicrobial properties to LDPE films while the vitamin E increased the oxidation induction period, especially for materials containing chitosan nanocomposites. The incorporation of both chitosan nanocomposites and vitamin E in polyethylene gave films with good antimicrobial and thermal properties because of significant increase of charge surface and important changes in surface topology and antimicrobial activity because of a synergistic effect. The nanocomposites cannot only passively protect the food against environmental factors, but they may enhance shelf life of food products.     

Fracture mechanisms of epoxy-based ternary composites filled with rigid-soft particles

Epoxy composites filled with different amounts of aggregate-free silica nanoparticles and phase-separated submicron rubber particles were fabricated to study the synergistic effect of multi-phase particles on mechanical properties of the composites. Compared with binary composites with single-phase particles, the ternary composites with both rigid and soft particles offer a good balance in stiffness, strength and fracture toughness, showing capacities in tailoring the mechanical properties of modified epoxy resins. It was observed that debonding of silica nanoparticles from matrix in the ternary composites was less pronounced than that in the binary composites. Moreover, the rubber particles became smaller and their shape tends to be irregular, affected by the presence of rigid silica nanoparticles. The toughening mechanisms in the epoxy composites were evaluated, and the enlarged plastic deformation around the crack tip, induced by the combination of rigid and soft particles, seems to be a dominant factor in enhancing fracture toughness of the ternary composites.     

Enhancement of fracture toughness,mechanical and thermal properties of rubber/epoxy composites by incorporation of graphene nanoplatelets

Carboxyl terminated butadiene acrylonitrile (CTBN) was added to epoxy resins to improve the fracture toughness, and then two different lateral dimensions of graphene nanoplatelets (GnPs), nominally <1 μm (GnP-C750) and 5 μm (GnP-5) in diameter, were individually incorporated into the CTBN/epoxy to fabricate multi-phase composites. The study showed that GnP-5 is more favorable for enhancing the properties of CTBN/epoxy. GnPs/CTBN/epoxy ternary composites with significant toughness and thermal conductivity enhancements combined with comparable stiffness to that of the neat resin were successfully achieved by incorporating 3 wt.% GnP-5 into 10 wt.% CTBN modified epoxy resins. According to the SEM investigations, GnP-5 debonding from the matrix is suppressed due to the presence of CTBN. Nevertheless, apart from rubber cavitation and matrix shear banding, additional active toughening mechanisms induced by GnP-5, such as crack deflection, layer breakage and separation/delamination of GnP-5 layers contributed to the enhanced fracture toughness of the hybrid composites.     

Interfacial,fire retardancy,and thermal stability evaluation of graphite oxide (GO)-phenolic composites with different GO particle sizes

Mechanical and thermal properties of graphite oxide (GO)-phenolic composites were evaluated for different sizes of GO. Tensile tests on the composites with larger sizes of GO particles typically exhibited better mechanical properties. After ageing tests at 200 °C a decline in the mechanical properties of GO-phenolic composites was observed but this decline was less than that for neat phenolic resin. This was attributed to the GO absorbing thermal energy and thereby reducing damage to the molecular chain in the resin. The ageing tests, also suggested that the wettability of specimens improved with the addition of GO, which might be attributed to microvoid formation on specimen’s surface during the elapsed time at the elevated temperature. The chemical structures of neat phenolic resin was relatively easily broken-up by thermal damage, whereas GO-phenolic composites exhibited better thermal stability in both thermal analysis and flame retardant testing. The GO particles exhibited reinforcing effects that served to protect chemical bonding in the phenolic resin. It appears, therefore, that GO composites may be good candidates for us as heat and flame resisting materials, for various applications.     

Non-stoichiometric curing effect on fracture toughness of nanosilica particulate-reinforced epoxy composites

Non-stoichiometric curing effects on the fracture toughness behaviors of nanosilica particulate-reinforced epoxy composites were experimentally investigated in this study by comparing them with bending strengths to take into consideration the effect of interaction between nanoparticles and network structures in matrix resins. The matrixes were prepared by curing them with an excess mixture of diglycidyl ether of bisphenol A-type epoxy resin as the curing agent for the stoichiometric condition. The volume fractions of the silica particles with a median diameter of 240 nm were constantly 0.2 for all composites. The neat epoxy resins and the composites were cured non-stoichiometrically to change the crosslinking densities of the neat epoxy resins and the matrix resins of the composites within 2740–490 mol/m³. The fracture toughnesses and bending strengths of the composites and the neat epoxy resins strongly depended on the crosslinking densities in the resins. Although the fracture toughness decreased monotonously from that of the stoichiometrically cured resins as the crosslinking density decreased, the fracture toughnesses of composites were largest at a slightly lower crosslinking density of approximately 2490 mol/m³ from the stoichiometric condition of 2740 mol/m³. The fracture toughness and the bending strength were improved for crosslinking densities higher than 2000 mol/m³ by adding particles. At crosslinking density lower than 2000 mol/m³, the particles worked against the mechanical properties as defects in matrix resins.     

Electrical and mechanical properties of antistatic PVC films containing multi-layer graphene

In order to explore practical application of graphene as novel conductive fillers in the filed of composite materials, we prepared anti-static multi-layer graphene (MLG) filled poly(vinyl chloride) (PVC) composite films by using conventional melt-mixing method, and investigated electrical conductivity, tensile behavior, and thermal properties of the MLG/PVC composite films. We found that the presence of MLG can greatly increase electrical conductivity of the MLG/PVC composites, and the surface electrical conductivity of the MLG/PVC composites is less than 3 × 10⁸ Ohm/square when the MLG loading is about 3.5 wt%, meeting anti-static requirement for commercial anti-static PVC films. On the other hand, the MLG/PVC composites exhibited higher tensile modulus and higher glass transition temperature than neat PVC, which is closely associated with crumpled morphology of the MLG and good compatibility between components of the MLG/PVC composites. By virtue of its satisfied anti-static performance and high mechanical properties, the MLG/PVC composites exhibit great potential to be used as high-performance antistatic materials in many fields.     

Mechanical properties of epoxy composites filled with silane-functionalized graphene oxide

In this work, the effects of as-produced GO and silane functionalized GO (silane-f-GO) loading and silane functionalization on the mechanical properties of epoxy composites are investigated and compared. Such silane functionalization containing epoxy ended-groups is found to effectively improve the compatibility between the silane-f-GO and the epoxy matrix. Increased storage modulus, glass transition temperature, thermal stability, tensile and flexural properties and fracture toughness of epoxy composites filled with the silane-f-GO sheets are observed compared with those of the neat epoxy and GO/epoxy composites. These findings confirm the improved dispersion and interfacial interaction in the composites arising from covalent bonds between the silane-f-GO and the epoxy matrix. Moreover, several possible fracture mechanisms, i.e. crack pinning/deflection, crack bridging, and matrix plastic deformation initiated by the debonding/delamination of GO sheets, were identified and evaluated.     

Effect of additive content on transient liquid phase sintering in SiC nanopowder infiltrated SiCf/SiC composites

SiC nanopowder infiltrated SiC_f/SiC composites with a high fiber volume fraction above 50 vol.% were prepared at a relatively low fabrication temperature of 1800 °C by transient liquid phase sintering using Al₂O₃-Y₂O₃-SiO₂ additives. The effects of additive content with 6-18 wt.% were investigated, based on densification, microstructure, mechanical properties and fracture behaviors of the composites. The results showed that the densification and mechanical properties of the composites were greatly improved with the additive content. Microstructural observation indicated that the infiltration of SiC nanopowder inside fiber-bundles were enchanced with the increase of additive content due to the effectively widen space by the reaction between pyrocarbon (PyC) interface and the additives especially with the addition of SiO₂. It proven that the enchanced matrix-PyC interface bonding by the high densification inside fiber-bundles played a key role in the improved mechanical properties and fracture behaviors of the composites.     

Preparation and properties of powder styrene-butadiene rubber composites filled with carbon black and carbon nanotubes

Carbon nanotubes (CNTs) and carbon black (CB) filled powder styrene-butadiene rubber (SBR) composites were prepared by spray drying of the suspension of CNTs and CB in SBR latex. The powders were sphere like and fine with uniform diameters of 10-15 μm. Experimental results showed that the introduction of CNTs into the matrix was beneficial to improve the security of the vulcanization of the rubber composites, and the dynamic and basic mechanical properties of the CNTs/SBR composites were better than those of CB/SBR and neat SBR composites. Observations on the microstructure of the composites indicated that CNTs were well dispersed in the matrix. Morphology of the fracture confirmed that the bonding between CNTs and rubber matrix was strong and load can be transferred to CNTs efficiently during the mechanical property tests. Moreover, the powder SBR composites containing well-dispersed CNTs could be perfect candidate as additives for other polymers.     

Mechanical and thermal properties of carbon fiber/polypropylene composite filled with nano-clay

The effect of organoclay on the mechanical and thermal properties of woven carbon fiber (CF)/compatibilized polypropylene (PPc) composites is investigated. Polypropylene–organoclay hybrids nanocomposites were prepared using a maleic anhydride-modified PP oligomer (PP-g-MA) as a compatibilizer. Different weight percentages of Nanomer® I-30E nanoclay were dispersed in PP/PP-g-MA (PPc) using a melt mixing method. The PPc/organoclay nanocomposite was then used to manufacture plain woven CF/PPc nanocomposites using molding compression process. CF/PPc/organoclay composites were characterized by different techniques, namely; dynamic mechanical analysis (DMA), fracture toughness and scanning electron microscope. The results revealed that at filler content 3% of organoclay, initiation and propagation interlaminar fracture toughness in mode I were improved significantly by 64% and 67% respectively, which could be explained by SEM at given weight as well; SEM images showed that in front of the tip, fibers pull out during initiation delamination accounting for fracture toughness improvement. Dynamic mechanical analysis showed enhancement in thermomechanical properties. With addition 3 wt.% of organoclay, the glass transition temperature increased by about 6 °C compared to neat CF/PPc composite indicating better heat resistance with addition of organoclay.     

Effect of graphene oxide on the physical,mechanical and thermo-mechanical properties of neoprene and chlorosulfonated polyethylene vulcanizates

The present research work demonstrated the effect of graphene oxide (GO) on the physical, mechanical, thermo-mechanical etc., properties of neoprene (CR) and chlorosulfonated polyethylene (CSPE) vulcanizates. CR and CSPE based nanocomposites were prepared by both solution intercalation and melt intercalation methods. The changes obtained in the morphology, cure characteristics, mechanical, thermal, thermo-mechanical properties of the rubber nanocomposites have been widely investigated. X-ray diffraction analysis (XRD) and transmission electron microscopic (TEM) analysis of the samples revealed partial exfoliated structure of GO containing rubber composites. Mechanical, thermal, cure and thermo-mechanical properties of the elastomeric nanocomposites were improved compared to the neat rubbers.     

Mechanical properties of 3D KD-I SiCf/SiC composites with engineered fibre-matrix interfaces

Three-dimensional (3D) silicon carbide (SiC) matrix composites reinforced with KD-I SiC fibres were fabricated by precursor impregnation and pyrolysis (PIP) process. The fibre-matrix interfaces were tailored by pre-coating the as-received KD-I SiC fibres with PyC layers of different thicknesses or a layer of SiC. Interfacial characteristics and their effects on the composite mechanical properties were evaluated. The results indicate that the composite reinforced with as-received fibre possessed an interfacial shear strength of 72.1 MPa while the composite reinforced with SiC layer coated fibres had a much higher interfacial shear strength of 135.2 MPa. However, both composites showed inferior flexural strength and fracture toughness. With optimised PyC coating thickness, the interface coating led to much improved mechanical properties, i.e. a flexural strength of 420.6 MPa was achieved when the interlayer thickness is 0.1 μm, and a fracture toughness of 23.1 MPa m^1/2 was obtained for the interlayer thickness of 0.53 μm. In addition, the composites prepared by the PIP process exhibited superior mechanical properties over the composites prepared by the chemical vapour infiltration and vapour silicon infiltration (CVI-VSI) process.     

Nanocomposites based on polystyrene-b-poly(ethylene-r-butylene)-b-polystyrene and exfoliated graphite nanoplates: Effect of nanoplatelet loading on morphology and mechanical properties

Exfoliated graphite nanoplates (xGnPs)/polystyrene-b-poly(ethylene-r-butylene)-b-polystyrene (SEBS) nanocomposites have been prepared by the simple melt-compounding approach. The structural, mechanical and viscoelastic properties of these composites were studied and compared. Wide-angle X-ray diffraction (WAXD) studies indicated that the processing of nanocomposites did not change the original d-spacing of xGnPs. Scanning electron microscopy observation on the fracture surfaces of the composites shows a uniform dispersion of xGnPs throughout SEBS matrix and strong interfacial adhesion between oxidized xGnPs and the matrix, which are responsible for the considerable enhancement of mechanical properties of the composites. It is found that the addition of xGnPs particles improved both the elastic modulus and storage modulus of pure SEBS significantly and the higher the xGnPs content, the higher the modulus of the nanocomposite. Moreover, the effects of dispersed xGnPs on the microphase separation of SEBS have also been investigated using small angle X-ray scattering (SAXS).     

Experimental investigation of carbon fiber reinforced poly(phenylene sulfide) composites prepared using a double-belt press

The high-performance carbon fiber reinforced poly(phenylene sulfide) composites were continuously fabricated using thermoplastic prepregs in a double-belt press. The effects of process velocity on the composite consolidation quality and mechanical properties were investigated. It is found that the tensile and interlaminar shear properties of composites prepared using the double-belt press are comparable to that of compression-molded composites when the process velocity is no more than 0.20 m·min⁻¹. The composite fracture morphologies also show different failure mechanisms between different samples and indicate that the interfacial adhesion strength may play a vital role in the mechanical properties of CF/PPS composites. Furthermore, experimental results show that the heating time above 330 °C should be over 440 s and the void content should be lower than 2.38% in order to obtain high performance CF/PPS composites.     

Nano-epoxy resins containing electrospun carbon nanofibers and the resulting hybrid multi-scale composites

For the first time, electrospun carbon nanofibers (ECNFs, with diameters and lengths of ∼200 nm and ∼15 μm, respectively) were explored for the preparation of nano-epoxy resins; and the prepared resins were further investigated for the fabrication of hybrid multi-scale composites with woven fabrics of conventional carbon fibers via the technique of vacuum assisted resin transfer molding (VARTM). For comparison, vapor growth carbon nanofibers (VGCNFs) and graphite carbon nanofibers (GCNFs) were also studied for making nano-epoxy resins and hybrid multi-scale composites. Unlike VGCNFs and GCNFs that are prepared by bottom-up methods, ECNFs are produced through a top-down approach; hence, ECNFs are more cost-effective than VGCNFs and GCNFs. The results indicated that the incorporation of a small mass fraction (e.g., 0.1% and 0.3%) of ECNFs into epoxy resin would result in substantial improvements on impact absorption energy, inter-laminar shear strength, and flexural properties for both nano-epoxy resins and hybrid multi-scale composites. In general, the reinforcement effect of ECNFs was similar to that of VGCNFs, while it was higher than that of GCNFs.     

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.     

Dispersion control and characterization in multiwalled carbon nanotube and phenylethynyl-terminated imide composites

The inherent multifunctional properties of carbon nanotubes provide an opportunity to create novel composites, but their dispersion into a polymer matrix is challenging due to nanotube dimensions, interparticle forces, and poor interaction with the polymer. In this study, we used melt mixing to disperse multiwalled carbon nanotubes (MWNTs) in a polyimide resin under various process conditions to understand the efficacy of the process and the energy required to achieve dispersion and distribution. Through controlled variation of process conditions, we achieved various degrees of nanotube dispersion and distribution. The different dispersion and distribution states were observed by microscopy and correlated with the magnitude of the changes seen in the glass transition temperature and viscosity when compared to the neat resin. The results of these studies will be used to assess the compatibility of nanocomposite resins with composite fabrication methods and predict appropriate processing conditions for producing multiscale composites.     

Mechanical properties of nano-silica particulate-reinforced epoxy composites considered in terms of crosslinking effect in matrix resins

In this study, the mechanical properties of nano-silica particulate-reinforced epoxy composites with different crosslinking densities were clarified experimentally to consider the interaction effects between nano-particles and the network structure in matrix resin. The matrices were prepared by curing with an excessive mixture of diglycidyl ether of bisphenol A type epoxy resin as the curing agent for the stoichiometric condition. The volume fraction of the silica particles with a median diameter of 240 nm was constantly 0.2 for every composite. The crosslinking densities and glass transition temperatures of the neat epoxy resins were identified from thermo-viscoelastic properties measured by dynamic mechanical analysis. Elastic moduli and strengths of the composites and the neat epoxy resins were measured by three-point bending tests. The glass transition temperatures of the neat epoxy resins decreased linearly as the crosslinking densities decreased from the stoichiometric condition. The glass transition temperatures of the composites were reduced by adding the nano-silica particles. The bending moduli of the composites in the glassy state could be predicted by using a mixture law of the composites regardless of the crosslinking densities and glass transition temperatures. The bending strengths were found to be sensitive to the crosslinking densities: they were both higher (for composites with high crosslinking densities) and lower (for composites with low crosslinking densities) than those of the neat epoxy resin. These results demonstrate that the interaction between nano-particles and network structures reduces the bending strengths, especially for low crosslinking densities.     

Ternary nano-CaCO3/poly(ethylene terephthalate) fiber/polypropylene composites: Increased impact strength and reinforcing mechanism

The binary nano-CaCO₃/polypropylene (PP), poly(ethylene terephthalate) (PET) fibers/PP and ternary nano-CaCO₃/PET fibers/polypropylene composites were prepared by melt blending method, and their structure and mechanical properties were investigated. The results show that the ternary nano-CaCO₃/PET fibers/PP composite displays significantly enhanced mechanical properties compared with the binary PET fibers/PP and nano-CaCO₃/PP composites, and neat PP. The X-ray diffraction, dynamic mechanical analysis, scanning electron microscopy and analysis of the non-isothermal crystallization kinetics were used to investigate the reinforcement mechanism of composites. The results indicate that the interfacial action and compatibility between PET fiber and PP are obviously enhanced by the addition of modified nano-CaCO₃ particles in the ternary composites and the mechanical property enhancement in the ternary system may be mainly originated from the formation of β-form crystallites of PP induced by the synergistic effect between PET fibers and nano-CaCO_3.     

Effect of diisocyanates as compatibilizer on the properties of ramie/poly(lactic acid) (PLA) composites

Ramie/PLA composites with the diisocyanates as compatibilizer were fabricated by extrusion and injection molding. The influence of different diisocyanates and various diisocyanate content on the mechanical properties and thermal properties of the composites was investigated. The presence of the diisocyanates in the composites lead to the improvements in mechanical properties and thermal properties of the composites. The morphologies of fracture surface using scanning electron microscopy (SEM) provided evidence of improved interfacial adhesion between ramie and PLA from the addition of the diisocyanates. The composites containing isophorone diisocyanate (IPDI) showed the best mechanical properties. The comparison of various IPDI content showed that the composites with 1.5% IPDI could get the optimum mechanical properties, and the excess diisocyanate content resulted in the decrease in the mechanical properties of the composites. However, IPDI content had almost no effect on the crystallization and melting behavior of the ramie/PLA composites.