Effects of extrusion temperature on the rheological,dynamic mechanical and tensile properties of kenaf fiber/HDPE composites

The effects of extrusion processing temperature on the rheological, dynamic mechanical analysis and tensile properties of kenaf fiber/high-density polyethylene (HDPE) composites were investigated for low and high processing temperatures. The rheological data showed that the complex viscosity, storage and loss modulus were higher with high processing temperature. Complex viscosities of pure HDPE and 3.4 wt% composite with zero shear viscosity of ⩽2340 Pa s were shown to exhibit Newtonian behavior while composites of 8.5 and 17.5 wt% with zero shear viscosity ⩾30,970 Pa s displayed non-Newtonian behavior. The Han plots revealed the sensitivity of rheological properties with changes in processing temperature. An increase in storage and loss modulus and a decrease in mechanical loss factor were observed for 17.5 wt% composites at high processing temperature and not observed at low processing temperature. Processing at high temperature was found to improve the tensile modulus of composites but displayed diminished properties when processed at low processing temperature especially at high fiber content. At both low and high processing temperatures, the tensile strength and strain of the composite decreased with increased content of the fiber.     

The effect of graphene presence in flame retarded epoxy resin matrix on the mechanical and flammability properties of glass fiber-reinforced composites

The effect of adding graphene in epoxy containing either an additive (MP) or reactive-type (DOPO) flame retardant on the thermal, mechanical and flammability properties of glass fiber-reinforced epoxy composites was investigated using thermal analysis; flexural, impact, tensile tests; cone calorimetry and UL-94 techniques. The addition of MP or DOPO to epoxy had a thermal destabilization effect below 400 °C, but led to higher char yield at higher temperatures. The inclusion of 10 wt% flame retardants slightly decreased the mechanical behavior, which was attributed to the poor interfacial interactions in case of MP or the decreased cross-linking density in case of DOPO flame retarded resin. The additional graphene presence increased flexural and impact properties, but slightly decreased tensile performance. Adding graphene further decreased the PHRR, THR and burning rate due to its good barrier effect. The improved fire retardancy was mainly attributed to the reduced release of the combustible gas products.     

Soybean oil-based thermosets with N-vinyl-2-pyrrolidone as crosslinking agent for hemp fiber composites

Soybean oil-based thermosets from acrylated epoxidized soybean oil (AESO) with a highly reactive vinyl monomer, N-vinyl-2-pyrrolidone (NVP), as crosslinking agent to replace styrene (St) were formulated for the fabrication of hemp fiber composites. The theoretical miscibility of NVP–AESO and St–AESO systems were discussed based on the group contribution method. The AESO resin with 30 wt% NVP exhibited a slightly higher viscosity than the counterpart with St, while the maximum curing temperature of the former was considerably lower than that of the latter. The composites from 20 wt% NVP resin gained comparable mechanical properties and higher glass transition temperature (T_g) to the composites with 30 wt% St. Further increase in NVP usage to 40 wt% resulted in the composites with higher tensile strength, tensile modulus, flexural strength, flexural modulus, storage modulus, and T_g of 29.6%, 22.4%, 22.5%, 20.6%, 21.6%, and 47.2%, respectively, when compared to those of the St-based composites.     

The effect of reprocessing on the mechanical properties of polypropylene reinforced with wood pulp,flax or glass fibre

Composites of polypropylene, substitutable for a given application and reinforced with: Medium Density Fibreboard fibre (MDF) (40 wt%); flax (30 wt%); and glass fibre (20 wt%), were evaluated after 6 injection moulding and extrusion reprocessing cycles. Of the range of tensile, flexural and impact properties examined, MDF composites showed the best mean property retention after reprocessing (87%) compared to flax (72%) and glass (59%). After 1 reprocessing cycle the glass composite had higher tensile strength (56.2 MPa) compared to the MDF composite (44.4) but after 6 cycles the MDF was stronger (35.0 compared to 29.6 MPa for the glass composite). Property reductions were attributed to reduced fibre length. MDF fibres showed the lowest reduction in fibre length between 1 and 6 cycles (39%), compared to glass (51%) and flax (62%). Flax fibres showed greater increases in damage (cell wall dislocations) with reprocessing than was shown by MDF fibres.     

Influence of the process parameters on the mechanical properties of engineering biocomposites using a twin-screw extruder

The utilization of bio-based engineering polymers as a matrix material for cellulosic fiber reinforced composites has become an important focus in materials research. This is due to a rising demand for sustainable materials from renewable resources. In addition to this aspect, the bio-based materials provide an advantage for lightweight applications with their lower density. In this investigation, the completely bio-based polyamide 10.10, with a melting point above 200 °C, was used as a polymer matrix. Chopped man-made cellulose fibers (Cordenka CR-Type) were investigated as reinforcement for use in injection molded applications. A co-rotating twin-screw extruder with a screw-diameter of 18 mm was used for compounding. It was verified that reinforcing polyamide 10.10 with 20 wt% and 30 wt% cellulosic fibers is possible, resulting in an increase of impact and tensile properties. Furthermore, it was shown that the temperatures and screw-configurations of the twin-screw extruder only result in different fiber length distributions but in minor differences of the morphological structure and mechanical properties of PA 10.10 with 20 wt% fibers. Compounds with 30 wt% cellulose fibers show significant higher impact properties that those with 30 wt% glass fibers.     

Strong and optically transparent biocomposites reinforced with cellulose nanofibers isolated from peanut shell

Cellulose nanofibers–reinforced PVA biocomposites were prepared from peanut shell by chemical–mechanical treatments and impregnation method. The composite films were optically transparent and flexible, showed high mechanical and thermal properties. FE-SEM images showed that the isolated fibrous fragments had highly uniform diameters in the range of 15–50 nm and formed fine network structure, which is a guarantee of the transparency of biocomposites. Compared to that of pure PVA resin, the modulus and tensile strength of prepared nanocomposites increased from 0.6 GPa to 6.0 GPa and from 31 MPa to 125 MPa respectively with the fiber content as high as 80 wt%, while the light transmission of the composite only decreased 7% at a 600 nm wavelength. Furthermore, the composites exhibited excellent thermal properties with CTE as low as 19.1 ppm/K. These favorable properties indicated the high reinforcing efficiency of the cellulose nanofibers isolated from peanut shell in PVA composites.     

Synthesis of H2Ti2O3·H2O nanotubes and their effects on the flame retardancy of bamboo fiber/high-density polyethylene composites

H₂Ti₂O₃·H₂O nanotubes (TNTs) were prepared through hydrothermal synthesis and dispersed in bamboo fiber/HDPE (BH) composites to improve the flame retardancy of the composites. TEM observation showed that TiO₂ particles were transformed into TNTs through hydrothermal treatment at 120 °C for 12 h in 8 M NaOH solution. Then, a cone calorimeter and a limiting oxygen index chamber were used to evaluate the effects of the TNTs on the flame retardancy of the BH composites. Results demonstrated that TNTs definitely improved the flame retardancy of BH composites by absorbing decomposition products from combustion due to its large specific area and tubular structure. Additionally, the TNTs reduced the free volume in the microzone, strengthened the molecular chain rigidity, and then contributed to the thermostability and flame retardancy of the BH composites.     

High thermal and mechanical properties enhancement obtained in highly filled polybenzoxazine nanocomposites with fumed silica

Highly filled polybenzoxazine nanocomposites filled with nano-SiO₂ particles were investigated for their mechanical and thermal properties as a function of filler loading. The nanocomposites were prepared by high shear mixing followed by compression molding. A very low A-stage viscosity of benzoxazine monomer gives it excellent processability having maximum nano-SiO₂ loading as high as 30 wt% (18.8 vol%) with negligible void content. Moreover, thermal analysis of the curing process of the compound of the PBA-a/nano-SiO₂ composites was found to be autocatalytic in nature with average activation energy of 79–92 kJ mol⁻¹. Microscopic analysis (SEM) performed on the PBA-a/nano-SiO₂ composite fracture surface indicated a nearly homogeneous distribution of the nano-scaled silica in the polybenzoxazine matrix. In addition, the enhancement in storage modulus of the nano-SiO₂ filled polybenzoxazine composites was found to be significantly higher than that of the recently reported nano-SiO₂ filled epoxy composites. The dependence of the nanocomposites’ modulus on the nano-SiO₂ particles content is well fitted by the generalized Kerner equation. Furthermore, the relatively high micro-hardness of the PBA-a/nano-SiO₂ composites up to about 600 MPa was achieved. Finally, the substantial enhancement in the glass transition temperature (T_g) of the PBA-a/nano-SiO₂ composites was also observed with the ΔT_g up to 16 °C at the nano-SiO₂ loading of 30 wt%. The resulting PBA-a/nano-SiO₂ composite is a highly attractive candidate as coating material in electronic packaging or other related applications.     

Effects of temperature and clay content on water absorption characteristics of modified MMT clay/cyclic olefin copolymer nanocomposite films: Permeability,dynamic mechanical properties and the encapsulated organic device performance

In the present study, amino-silane modified layered organosilicates were used to reinforce cyclic olefin copolymer to enhance the thermal, mechanical and moisture impermeable barrier properties. The optimum clay loading (4%) in the nanocomposite increases the thermal stability of the film while further loading decreases film stability. Water absorption behavior at 62 °C was carried out and compared with the behavior at room temperature and 48 °C. The stiffness of the matrix increases with clay content and the recorded strain to failure for the composite films was lower than the neat film. Dynamic mechanical analysis show higher storage modulus and low loss modulus for 2.5–4 wt% clay loading. Calcium degradation test and device encapsulation also show the evidence of optimum clay loading of 4 wt% for improved low water vapor transmission rates compared to other nanocomposite films.     

New development of self-damping MWCNT composites

Epoxy resin modified with nanofillers cannot be used alone for high performance structural applications due to their low-mechanical properties. Therefore, the objective of this work is to hybridize unidirectional and quasi-isotropic glass fiber composite laminates with 1.0 wt% multi-walled carbon nanotubes (MWCNTs). Results from flexural and damping characterizations showed that the flexural strength and modulus, storage modulus, and damping ratio of MWCNT/E nanocomposite are improved by about 7% ± 1.5% compared to neat epoxy. The enhancement in the flexural strength of quasi-isotropic laminate (20.7%) is about ten times higher than that for unidirectional laminate (2.1%). The flexural moduli of the nano-hybridized laminates are reduced by about 7.5–10.8%. Accordingly, the ultimate failure strain and damping properties are evidently improved. The improvement in damping ratio in some cases is about 100%. The high correlation coefficient (0.9995) between flexural and storage moduli suggests using the dynamic nondestructive tests for evaluation the elastic properties of composites.     

The effect of alkaline treatment on mechanical properties of kenaf fibers and their epoxy composites

In this work, kenaf fibers were pre-treated in a NaOH solution (6% in weight) at room temperature for two different periods (48 and 144 h). The chemical treatment of kenaf fibers for 48 h allowed to clean their surface removing each impurity whereas 144 h of immersion time had detrimental effect on the fibers surface and, consequently, on their mechanical properties.Untreated and NaOH treated kenaf fibers (i.e. for 48 h) were also used as reinforcing agent of epoxy resin composites. The effect of the stacking sequence (i.e. using unidirectional long fibers or randomly oriented short fibers) and the chemical treatment on the static mechanical properties was evaluated showing that the composites exhibit higher moduli in comparison to the neat resin. As regards the strength properties, only the composites reinforced with unidirectional layers show higher strength than the neat resin. Moreover, the alkali treatment increased the mechanical properties of the composites, due to the improvement of fiber–matrix compatibility.The dynamic mechanical analysis showed that the storage and the loss moduli are mainly influenced by the alkali treatment above the glass transition temperature. Moreover, the alkali treatment led to a notable reduction of tan δ peaks in addition to significant shifts of tan δ peaks to higher temperatures whereas the stacking sequence did not influence the trends of storage modulus, loss modulus and damping of the composites.     

Introducing cellulose nanocrystals in sheet molding compounds (SMC)

The mechanical properties of short glass fiber/epoxy composites containing cellulose nanocrystals (CNC) made using sheet molding compound (SMC) manufacturing method as well as the rheological and thermomechanical properties of the CNC-epoxy composites were investigated as a function of the CNC content. CNC up to 1.4 wt% were dispersed in the epoxy to produce the resin for SMC production. The addition of CNC in the resin increased its viscosity and slightly reduced the heat of reaction during the polymerization without altering the curing time and temperature and the effective pot life of the resin. The incorporation of 0.9 wt% CNC in the SMC composite resulted in increases in elastic modulus and tensile strength by ∼25% and ∼30% and in flexural modulus and strength by ∼44% and ∼33% respectively. Concentrations of CNC up to 0.9 wt% in the SMC composite did not alter the impact energy.     

Thermal and mechanical properties of polyamide 11 based composites reinforced with surface modified titanate nanotubes

The preparation of polyamide 11 (PA11) based composites reinforced with pristine and surface-modified titanate nanotubes (TTNT) is reported. Twin-screw melt compounding was used to produce composites with up to 2 wt% of TTNT. To enhance dispersion and TTNT compatibility with the thermoplastic, these were modified with cetyltrimethylammonium bromide (CTAB) and sodium dodecyl sulphate (SDS). Fourier transform infrared spectroscopy and thermogravimetry were used to demonstrate that surface modification prior to composite processing was successful, while scanning transmission electron microscopy combined with energy-dispersive X-ray analysis confirmed the retention of surfactants on TTNT in composites. Nevertheless, scanning and transmission electron microscopy revealed incomplete dispersion of TTNT inside polyamide. The improved wettability on the TTNT–PA11 interface was observed for composites comprising surface-modified TTNT. Consequently, these composites exhibited better thermal and mechanical properties than those containing pristine TTNT. A significant rise of the decomposition temperature was detected in composites containing TTNT modified with CTAB, while the uppermost increment of the storage and Young’s modulus (of about 35% and 26%, respectively) was achieved in the composite comprising 0.5 wt% of TTNT modified with SDS. The increase of the nanofiller content improved the yield strength and led to the drop in the strain at break.     

Enhanced mechanical,thermal and flame retardant properties by combining graphene nanosheets and metal hydroxide nanorods for Acrylonitrile–Butadiene–Styrene copolymer composite

Three metal hydroxide nanorods (MHR) with uniform diameters were synthesized, and then combined with graphene nanosheets (GNS) to prepare acrylonitrile–butadiene–styrene (ABS) copolymer composites. An excellent dispersion of exfoliated two-dimensional (2-D) GNS and 1-D MHR in the ABS matrix was achieved. The effects of combined GNS and MHR on the mechanical, thermal and flame retardant properties of the ABS composites were investigated. With the addition of 2 wt% GNS and 4 wt% Co(OH)₂, the tensile strength, bending strength and storage modulus of the ABS composites were increased by 45.1%, 40.5% and 42.3% respectively. The ABS/GNS/Co(OH)₂ ternary composite shows the lowest maximum weight loss rate and highest residue yield. Noticeable reduction in the flammability was achieved with the addition of GNS and Co(OH)₂, due to the formation of more continuous and compact charred layers that retarded the mass and heat transfer between the flame and the polymer matrix.     

Enhanced thermal conductivity and retained electrical insulation for polyimide composites with SiC nanowires grown on graphene hybrid fillers

Polyimide (PI) composites containing one-dimensional SiC nanowires grown on two-dimensional graphene sheets (1D–2D SiC_NWs-GSs) hybrid fillers were successfully prepared. The PI/SiC_NWs-GSs composites synchronously exhibited high thermal conductivity and retained electrical insulation. Moreover, the heat conducting properties of PI/SiC_NWs-GSs films present well reproducibility within the temperature range from 25 to 175 °C. The maximum value of thermal conductivity of PI composite is 0.577 W/mK with 7 wt% fillers loading, increased by 138% in comparison with that of the neat PI. The 1D SiC nanowires grown on the GSs surface prevent the GSs contacting with each other in the PI matrix to retain electrical insulation of PI composites. In addition, the storage modulus and Young’s modulus of PI composites are remarkably improved in comparison with that of the neat PI.     

The potential of harakeke fibre as reinforcement in polymer matrix composites including modelling of long harakeke fibre composite strength

Mechanical properties of aligned long harakeke fibre reinforced epoxy with different fibre contents were evaluated. Addition of fibre was found to enhance tensile properties of epoxy; tensile strength and Young’s modulus increased with increasing content of harakeke fibre up to 223 MPa at a fibre content of 55 wt% and 17 GPa at a fibre content of 63 wt%, respectively. The flexural strength and flexural modulus increased to a maximum of 223 MPa and 14 GPa, respectively, as the fibre content increased up to 49 wt% with no further increase with increased fibre content. The Rule of Mixtures based model for estimating tensile strength of aligned long fibre composites was also developed assuming composite failure occurred as a consequence of the fracture of the lowest failure strain fibres taking account porosity of composites. The model was shown to have good accuracy for predicting the strength of aligned long natural fibre composites.     

Hybridization effect on the mechanical properties of curaua/glass fiber composites

The aim of this paper was to evaluate the effect of hybridizing glass and curaua fibers on the mechanical properties of their composites. These composites were produced by hot compression molding, with distinct overall fiber volume fraction, being either pure curaua fiber, pure glass fiber or hybrid. The mechanical characterization was performed by tensile, flexural, short beam, Iosipescu and also nondestructive testing. From the obtained results, it was observed that the tensile strength and modulus increased with glass fiber incorporation and for higher overall fiber volume fraction (%V_f). The short beam strength increased up to %V_f of 30 vol.%, evidencing a maximum in terms of overall fiber/matrix interface and composite quality. Hybridization has been successfully applied to vegetable/synthetic fiber reinforced polyester composites in a way that the various properties responded satisfactorily to the incorporation of a third component.     

Using response surface methodology for modeling and optimizing tensile and impact strength properties of fiber orientated quaternary hybrid nano composite

In current study, weight percentage of nano silica and nano clay and also fiber orientation have been chosen as independent variables and the affect of these variables on tensile and izod impact strength of epoxy/glass fiber/SiO₂/clay hybrid laminate composite has been investigated. Central composite design (CCD) which is subset of response surface methodology has been employed to present mathematical models as function of physical factors to predict tensile and impact behavior of new mentioned hybrid nano composite and also optimizing mentioned mechanical properties. Totally 20 experiments were designed with 6 replicates at center point. The maximum and minimum value of tensile strength were 450.90 MPa and 158.16 MPa which occurred in design levels 1 and 14 respectively, also the maximum and minimum of izod impact strength were 10.47 kJ/m² and 2.56 kJ/m² which occurred in design levels 13 and 14 respectively. The optimization results using optimization part of Minitab software showed that the best tensile strength was obtained 488.53 MPa and occurred in 3.5 wt% of nano silica, 1.1 wt% of nano clay and 9° of fiber orientation and after preparing and testing five samples average value of tensile strength was obtained about 480 MPa. Also the results showed that the best impact strength obtained from software was 11.35 kJ/m² and occurred in 4.03 wt% of nano clay, 5 wt% of nano silica and 0° of fiber orientation. The optimization results also showed that tensile and impact strength at optimum values improved up to 6.4% and 203.5% compared to level 1 and 14 and 6.02% and 303.6% compared to level 13 and 14 respectively. In addition, the fracture surface morphologies of the quaternary nano composites were investigated by scanning electron microscopy (SEM).     

Effect of fiber loading on mechanical and morphological properties of cocoa pod husk fibers reinforced thermoplastic polyurethane composites

In this study, cocoa (Theobroma cacao) pod husk (CPH) fiber reinforced thermoplastic polyurethane (TPU) was prepared by melt compounding method using Haake Polydrive R600 internal mixer. The composites were prepared with different fiber loading: 20%, 30% and 40% (by weight), with the optimum processing parameters: 190 °C, 11 min, and 40 rpm for temperature, time and speed, respectively. Five samples were cut from the composite sheet. Mean value was taken for each composite according to ASTM standards. Effect of fiber loading on mechanical (i.e. tensile, flexural properties and impact strength) and morphological properties was studied. TPU/CPH composites showed increase in tensile strength and modulus with increase in fiber loading, while tensile strain was decreasing with increase in fiber loading. The composite also showed increase in flexural strength and modulus with increase in fiber content. Impact strength was deteriorated with increase in fiber loading. Morphology observations using Scanning Electron Microscope (SEM) showed fiber/matrix good adhesion.     

Reinforcing potential of micro- and nano-sized fibers in the starch-based biocomposites

Starch-based biocomposites reinforced with jute (micro-sized fiber) and bacterial cellulose (BC) (nano-sized fiber) were prepared by film casting. Reinforcement in the composites is essentially influenced by fiber nature, and amount of loading. The optimum amount of fiber loading for jute and bacterial cellulose in each composite system are 60 wt% and 50 wt% (of starch weight), respectively. Mechanical properties are largely improved due to the strong hydrogen interaction between the starch matrix and cellulose fiber together with good fiber dispersion and impregnation in these composites revealed by SEM. The composites reinforced with 40 wt% or higher bacterial cellulose contents have markedly superior mechanical properties than those reinforced with jute. Young’s modulus and tensile strength of the optimum 50 wt% bacterial cellulose reinforced composite averaged 2.6 GPa and 58 MPa, respectively. These values are 106-fold and 20-fold more than the pure starch/glycerol film. DMTA revealed that the presence of bacterial cellulose (with optimum loading) significantly enhanced the storage modulus and glass transition temperature of the composite, with a 35 °C increment. Thermal degradation of the bacterial cellulose component occurred at higher temperatures implying improved thermal stability. The composites reinforced with bacterial cellulose also had much better water resistance than those associated with jute. In addition, even at high fiber loading, the composites reinforced by bacterial cellulose clearly retain an exceptional level of optical transparency owing to the effect of the nano-sized fibers and also good interfacial bonding between the matrix and bacterial cellulose.