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.     

Preparation, characterisation and processing of carbon fibre/polyamide-12 composites for selective laser sintering

Aiming at developing carbon fibre/polyamide-12 (CF/PA) composite powders for manufacturing high-performance components by selective laser sintering (SLS), the preparation, characteristics and sintering process of the composite powders and mechanical properties of sintered components were studied. Surfaces of the carbon fibres were treated by the oxidation modification and coated with polyamide-12 through the dissolution-precipitation process to provide good interfacial adhesion and homogenous dispersion within the polyamide-12 matrix. The particle size and micro-morphology analyses show that the CF/PA composite powders with 30 wt%, 40 wt% and 50 wt% carbon fibres present the suitable powder sizes and format for SLS. The incorporation of carbon fibres into the polyamide-12 matrix decreases the initial melting temperature and consequently lowers the SLS part bed temperatures, implying lower energy requirement and less thermal degradation in the sintering process. The CF/PA composites also represent higher thermal stability than the pure polyamide-12. The CF/PA sintered components with 30 wt%, 40 wt% and 50 wt% carbon fibres exhibit the greatly enhanced flexural strengths by 44.5%, 83.3%, 114%, and the flexural modulus by 93.4%, 129.4%, 243.4%, respectively, as compared with the pure polyamide-12 sintered parts. Fractured surface analysis shows that the carbon fibres are encapsulated and bonded well with the polyamide matrix. The complex SLS parts with the thinnest wall of 0.6 mm, the density of 1.09 ± 0.02 g/cm³ and the relatively density of 94.13 ± 1.72% were manufactured using the CF/PA composite powder with 30 wt% carbon fibres. This study demonstrates that the CF/PA composite powders prepared by the surface treatment and dissolution-precipitation method represent suitable interfacial adhesion, filler dispersion, particle sizes and sintering behaviours for SLS and enable the manufacture of complex components with high performance.     

Layered silicates nanocomposite matrix for improved fiber reinforced composites properties

Three-phase glass fiber reinforced composites (GFRP) consisting of traditional woven glass fiber and polyamide-6 (PA6) matrix dispersed with organically modified layered silicates were prepared and investigated in this study. The fabrication of GFRP with different weight percentages of layered silicates was successful when the matrix contains less than 5 wt% of the layered silicates. The improvement due to the high aspect ratio and high stiffness of the layered silicates is illustrated through the matrix-controlled properties of the GFRP. The results showed that the GFRP with 5 wt% layered silicates offer the largest improvement of approximately 30% increase in both flexural strength and compressive strength at elevated temperatures. On the other hand, the in-plane shear properties measured from [±45]_s laminates revealed that the layered silicates help improved both the in-plane shear strength and modulus appropriately. By utilizing a nanocomposite matrix, improvement of stiffness and strength, as well as thermal and barrier properties is obtained without any change in processing temperature of the fiber composites.     

Enhancement of mechanical properties of waste-sourced biocomposites through peroxide induced crosslinking

The enhancement of mechanical performance of waste-sourced biocomposites through peroxide induced crosslinking was investigated in order to expand their range of applications. Biocomposites containing 25 to 35 wt% of residual Kraft-pulp cellulose fibers, 1.5 wt% of a selected maleic-anhydride-modified polyethylene coupling agent and a 60/40 (w/w) of recycled agricultural plastic/post-consumer plastic blend were compounded in an extrusion-compounding pilot-plant. Changes in the blend structure due to the presence of the organic peroxide used were studied by spectroscopy and thermal analysis. It was found that the addition of extremely low amounts of peroxide (0.025–0.050 wt%) results in remarkable improvements in stiffness, strength and toughness of biocomposites, without compromising processability. Thus, their tensile strength and energy at break increased up to 89.4% and 138%, respectively, with regard to uncrosslinked biocomposites. Scanning electron microscopy revealed an improvement of the fiber–matrix adhesion due to the treatment with the peroxide.     

Mechanical and fracture properties of ternary PE/PA6/GF composites

This article studies the mechanical properties of short fiber reinforced polymer blends comprised of a soft thermoplastic matrix (polyethylene, PE), a rigid dispersed thermoplastic phase (polyamide-6, PA6) and glass fiber reinforcement. These ternary composites are designed as a model system to investigate the impact of the mutual interactions of the three phases on the composite mechanical properties. For this purpose two types of fibers are used, dispersed-phase and matrix-phase compatible fibers, respectively.     

An exploratory study of GFRP rebar with ribs containing milled glass fibers

Surface deformations of GFRP rebars are important in developing mechanical anchorage. The mixture of epoxy resin and milled glass fibers is considered as an alternative for surface structure of GFRP rebar to enhance the bond with the concrete. In order to investigate the applicability of the surface structure, manufacturing, material tests, pullout tests and shear tests were conducted. The mixture was successfully applied and shaped onto the GFRP rebars when the milled fibers were mixed to be within 20–50 wt% of the mixture. The bond performance was enhanced by adding as much milled glass fibers as possible but up to a workable range. When the milled glass fiber content was 50%, the upper limit of mix ratio, bond strength to concrete was only 10% less than that of the ordinary steel rebar. In addition, under an accelerated alkalinity condition, the amounts of mixed milled glass fibers in surface deformations have a minor effect on the durability of the proposed GFRP rebar.     

Electrodeposition of exfoliated graphite nanoplatelets onto carbon fibers and properties of their epoxy composites

Exfoliated graphite nanoplatelet (xGnP)/copper (Cu) coated carbon fibers were fabricated by electrophoretic deposition under different applied voltages. The electrical and mechanical properties of individual fibers and composites made from these fibers and epoxy resin were investigated. The electrical resistivity of xGnP/Cu coated single carbon fiber is lower than that of the uncoated control sample and decreases with increase in the applied voltage. The xGnP and metallic Cu were simultaneously deposited on the carbon fiber surface as a result of the electrochemical cell configuration. The interfacial shear strength decreases with applied voltage up to 30 V but increases with applied voltage of over 30 V. The interfacial shear strength for the coated samples except the 50 V treated sample is lower than that of control sample. The flexural strength and modulus of xGnP/Cu coated carbon/epoxy composites is higher than those of control sample due to the reinforcing effect of xGnP/Cu coated on the carbon fibers.     

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.     

Influence of compatibilizing system on morphology,thermal and mechanical properties of high flow polypropylene reinforced with short hemp fibers

Simultaneous influence of polypropylene-graft-maleic anhydride (MAPP) and silane-treated hemp fibers (HF) on morphology, thermal and mechanical properties of high-flow polypropylene (PP) modified with poly[styrene-b-(ethylene-co-butylene)-b-styrene] (SEBS) was studied in this paper. The addition of SEBS reduced the efficiency of MAPP in PP composites with HF, thus silane-treated fibers (HFs) were used to improve polymer–fiber interface. Thermal stability of HF was improved after silane treatment and less than 2% weight loss was observed at 240 °C in composites with 30 wt% HF. Better dispersion of fibers and better efficiency in enhancing static and dynamic mechanical properties of PP, doubling its strength and stiffness were observed in composites with treated fibers compared to untreated ones. High ability to absorb and dissipate energy and well-balanced strength and stiffness were showed by PP modified with SEBS and MAPP containing 30 wt% HFs. These composites were studied as an alternative to conventional PP/glass fibers composites for injection molding of small to medium auto parts.     

Materials and mechanical properties of pretreated coir-based green composites

Chemical composition modification and surface modification of coir fibers are made in view of their use as reinforcement in coir-based green composites. Composites were prepared using coir fiber treated with varying pretreatment condition. The changes in the proportion of chemical composition and morphological properties of coir fibers with different coir pretreatment condition were discussed. It is observed that the mechanical properties of coir-based green composites; modulus of rupture and internal bond, increase as a result of chemical composition modification and surface modification. Scanning electron microscopy (SEM) investigations show that surface modifications improve the fiber/matrix adhesion.     

The effects of carbon nanotubes on mechanical and thermal properties of woven glass fibre reinforced polyamide-6 nanocomposites

This paper presents a preliminary investigation on the effects of incorporating carbon nanotubes (CNT) into polyamide-6 (PA6) on mechanical, thermal properties and fire performance of woven glass reinforced CNT/PA6 nanocomposite laminates. The samples were characterized by tensile and flexural tests, thermal gravimetric analysis (TGA), heat distortion temperature (HDT) measurements, thermal conductivity and cone calorimeter tests. Incorporation of up to 2 wt% CNT in CNT/PA6/GF laminates improved the flexural stress of the laminates up to 36%, the thermal conductivity by approximately 42% and the ignition time and peak HRR time was delayed by approximately 31% and 118%, respectively.     

Fiber-reinforced composite foam from expandable PVC microspheres

The properties of composite foam based on PVC expandable microspheres reinforced with continuous aramid fibers are described. The foam was fabricated by infiltrating low-density non-woven fiber webbing with PVC microspheres. The assembly was subsequently heated to expand the foam. The resulting composite foam consisted of 10 wt% aramid fibers and had a density of 100 kg/m³. Mechanical properties, crack propagation, and microstructure of composite foams were evaluated and compared with properties of similar unreinforced foam and with commercial PVC foam of comparable density. The influence of fiber concentration, fiber architecture and bonding was investigated also. Properties were measured in tension, shear, compression, and flexure using standard ASTM test methods. The composite foam performance equaled or surpassed the performance of most thermoplastic foams commercially available. The tensile strength and modulus of the composite foam increased by factors of 6 and 8, respectively, and the shear strength and modulus increased by factors of 1.8 and 2.4. The composite foam also exhibited improved strain energy density and damage tolerance, and reduced notch sensitivity.     

Expanded graphite nanoplatelets as coupling agents in glass fiber reinforced polypropylene composites

The interfacial adhesion between E-glass fibers and various types of nanomodified polypropylene (PP) matrices have been investigated on single-fiber model composites. In particular, an evaluation of the fiber–matrix interfacial shear strength was performed by the fragmentation tests on model composites prepared by using PP matrices containing various amounts (up to 7 wt%) of expanded graphite nanoplatelets (xGnP).The presence of xGnP in the polymer matrix resulted in a remarkable increase of the interfacial shear strength values (up to a factor of about 6 for a 7 wt% content of xGnP) if compared to neat PP. Moreover, wettability measurements in various liquids evidenced that the work of adhesion of the polymer matrix with respect to glass fiber, was improved by the presence of xGnP.     

Effect of fiber loading on the properties of treated cellulose fiber-reinforced phenolic composites

The effect of fiber loading on the properties of treated cellulose fiber-reinforced phenolic composites was evaluated. Alkali treatment of the fibers and reaction with organosilanes as coupling agents were applied to improve fiber–matrix adhesion. Fiber loadings of 1, 3, 5, and 7 wt% were incorporated to the phenolic matrix and tensile, flexural, morphological and thermal properties of the resulting composites were studied. In general, mechanical properties of the composites showed a maximum at 3% of fiber loading and a uniform distribution of the fibers in such composites was observed. Silane treatment of the fibers provided derived composites with the best thermal and mechanical properties. Meanwhile, NaOH treatment improved thermal and flexural properties, but reduced tensile properties of the materials. Therefore, the phenolic composite containing 3% of silane treated cellulose fiber was selected as the material with optimal properties.     

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.     

The effect of molecular weight on the interfacial properties of GF/PP injection molded composites

It is well established that the molecular weight of recycled PP decreases significantly as compared to the virgin material. Hence this study involved 2 PP grades of different molecular weights in order to simulate the recycling process. The effect of weight–average molecular weight on interfacial adhesion between GF and PP was investigated. Tensile test was done and the fiber length distribution around the fracture zone in both composites was compared with the distributions from similar locations of unstressed composites. The effect of PP-grafted maleic anhydride coupling agent was also studied. It was found that a decrease in weight–average molecular weight of PP improved interfacial adhesive strength between GF/PP. The lower molecular weight matrix has a lower viscosity that enables its molecules to penetrate easily into the silane interphase. In that case, the interfacial area that is available for coupling is higher, leading to a more effective coupling. The higher interfacial shear strength between the glass fiber and the lower molecular weight matrix induced more breakage of the glass fiber during tensile test.     

Glass fiber reinforced high glass transition temperature thiol–ene networks

Although thiol–ene polymers have highly desirable processing properties the networks usually are limited to having characteristically low glass transition temperatures with low strength. This study is one of the first studies to examine a thiol–ene polymer thermoset matrix, having many industrial advantages compared to conventional polymer matrices, reinforced with continuous E-glass fibers. In order to control the interphase, a mercapto functional sizing of 1 wt% is applied to the glass fibers. The resulting composites of 12 vol% fibers are comparable to glass fiber reinforced polyesters in terms of strength with Young’s modulus. This work contributes to the furthering of thiol–ene ultra-violet cure systems, with their range of advantageous properties, for use in a broader scope of applications by way of creating a stronger material based on a novel class of thermoset matrix.     

超高分子量聚乙烯纤维的液相氧化改性及其环氧树脂基复合材料的力学和摩擦性能

为增强超高分子量聚乙烯(UHMWPE)纤维与环氧树脂(EP)基体之间的界面粘结强度,采用重铬酸钾溶液对UHMWPE纤维进行表面改性并制备UHMWPE纤维/EP复合材料。结果表明,UHMWPE纤维经液相氧化后表面刻蚀痕迹明显,表面粗糙度明显增加,结晶度增加了11.3%,与乙二醇的接触角减小了14.12°。与纯环氧树脂相比,纤维含量为0.4%的未改性UHMWPE纤维/EP复合材料的拉伸强度降低18.04%,纤维含量为0.6%的液相氧化改性UHMWPE纤维/EP复合材料的拉伸强度降低51.55%,未改性UHMWPE(纤维含量0.5%)和液相氧化改性UHMWPE(纤维含量0.4%)纤维/EP复合材料的冲击强度分别提升了3.29%和4.39%。当纤维含量为0.3%时,液相氧化改性UHMWPE纤维/EP复合材料的弯曲强度比纯环氧树脂增加6.55%,比未改性UHMWPE纤维/EP复合材料增加19%。当纤维含量由0增大到0.5%时,改性和未改性UHMWPE纤维/EP复合材料的摩擦系数先增加后减小。     

Multiscale fiber reinforced composites based on a carbon nanofiber/epoxy nanophased polymer matrix: Synthesis, mechanical, and thermomechanical behavior

Vacuum assisted resin infusion molding (VARIM) was used to produce multiscale fiber reinforced composites (M-FRCs) based on carbon nanofibers dispersed in an epoxy resin. Flexural, interlaminar shear strength (ILSS) and thermomechanical tests are presented for the 0.1 wt% and 1 wt% M-FRCs and compared with the neat fiber reinforced composites (FRCs). Flexural strength and modulus increased (16–20%) and (23–26%), respectively for the 0.1 wt% and 1 wt% M-FRCs when compared to the neat FRCs. ILSS properties increased (6% and 25%) for the 0.1 wt% and 1 wt% M-FRCs, respectively when compared to neat FRCs. The glass transition temperatures (T_g) of both M-FRC samples were 25 °C higher than the neat FRC. Coefficients of thermal expansion (CTE) of the M-FRC samples improved compared to the neat FRC. The improved T_g and CTE properties in the M-FRC samples are attributed to synergistic interactions between the CNF/PNC matrix and glass fibers.     

Direct fluorination of Twaron fiber and the mechanical, thermal and crystallization behaviour of short Twaron fiber reinforced polypropylene composites

An experimental study of the incorporation of non-fluorinated and fluorinated Twaron fibers in polypropylene (PP) is presented. Surface modifications were made to Twaron fiber by direct fluorination technique using elemental fluorine in order to improve the interfacial adhesion between the fiber and matrix. Composites of PP/Twaron fiber (both Fluorinated and non-fluorinated) with 0.6%, 1.25%, 5% and 10% of Twaron fibers (w/w) were prepared by a solution method. Mechanical behaviour was estimated by the measurement of the tensile strength. The mechanical properties of PP improve significantly with the incorporation of Twaron fibers and fluorinated fiber composites show superior mechanical properties compared to the non-fluorinated system. The morphology was determined by scanning electron microscopy (SEM), showing good dispersion of the fibers. The thermal and crystallization behaviour of PP/Twaron fiber composites were studied by thermogravimetry (TG) and differential scanning calorimetry (DSC). The effect of fiber content and fiber surface treatments on the thermal properties was evaluated. DSC analysis exhibited an increase in the crystallization temperature and crystallinity, melting temperature upon the addition of fluorinated fibers to the PP matrix. This is attributed to the nucleating effects of the fiber surfaces. Also the thermal stability (from TG) and surface energy (determined from contact angle measurement) increased for fluorinated fiber composites. Surface modification of Twaron fibers leads to improved adhesion with the PP matrix and hence an improvement in properties of the Twaron fiber-PP composites.