Effect of chemical modifications of the pineapple leaf fiber surfaces on the interfacial and mechanical properties of laminated biocomposites

Natural fiber reinforced renewable resource based laminated composites were prepared from biodegradable poly(lactic acid) (PLA) and untreated or surface-treated pineapple leaf fibers (PALF) by compression molding using the film stacking method. The objective of this study was to determine the effects of surface treatment of PALF on the performance of the fiber-reinforced composites. X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) were used to aid in the analysis. The mechanical properties of the PLA laminated composites were improved significantly after chemical treatment. It was found that both silane- and alkali-treated fiber reinforced composites offered superior mechanical properties compared to untreated fiber reinforced composites. The effects of temperature on the viscoelastic properties of composites were studied by dynamic mechanical analysis (DMA). From the DMA results, incorporation of the PALF fibers resulted in a considerable increase of the storage modulus (stiffness) values. The heat defection temperature (HDT) of the PALF fiber reinforced PLA laminated composites was significantly higher than the HDT of the neat PLA resin. The differential scanning calorimeter (DSC) results suggest that surface treatment of PALF affects the crystallization properties of the PLA matrix. Additionally, scanning electron microscopy (SEM) was used to investigate the distribution of PLA within the fiber network. SEM photographs of fiber surface and fracture surfaces of composites clearly indicated the extent of fiber–matrix interface adhesion. It was found that the interfacial properties between the reinforcing PALF fibers and the surrounding matrix of the laminated composite are very important to the performance of the composite materials and PALF fibers are good candidates for the reinforcement fiber of high performance laminated biodegradable biocomposites.     

Henequen/poly(butylene succinate) biocomposites: electron beam irradiation effects on henequen fiber and the interfacial properties of biocomposites

Henequen natural fiber-reinforced poly(butylene succinate) biocomposites were prepared through a resin microdroplet formation on a single fiber and also fabricated by a compression molding technique using chopped henequen fibers, surface-treated with electron beam irradiation (EBI) at various dosages. The effect of EBI treatment on the surface characteristics and dynamic mechanical properties of henequen fibers was investigated using SEM, XPS and DMA methods, respectively. Also, the interfacial behavior of biocomposites was explored through a single fiber microbonding test and fracture surface observations. The result indicates that the interfacial shear strength (IFSS) of biocomposites greatly depends on the EBI treatment level on the henequen fiber surface. This study also suggests that appropriate modification of natural fiber surfaces at an optimum EBI dosage significantly contributes to improving the interfacial properties of biocomposites.     

Correlation of the mechanical properties to the fiber–matrix adhesion of Nextel 312™ fiber/BN/Blackglas™ composites

Boron nitride (BN)-coated aluminoborosilicate (Nextel? 312) fibers, produced via ammonia nitridation, along with 'as-received' and 'desized' fibers, were composited in a silicon oxycarbide (Blackglas?) matrix. The mechanical properties, failure properties, and fiber–matrix interfacial chemistry of the composite were investigated. BN treated fiber composites show a 90% improvement in flexural strength and substantial increases in shear strength (short beam shear and Iosipescu) over the 'as-received' fiber composite. The composite fabricated with 'desized' fibers underwent spontaneous delamination during pyrolization, precluding mechanical testing. X-ray photoelectron spectroscopy of the starting materials and of composite fracture surfaces combined with scanning electron microscopy and energy dispersive X-ray spectroscopy indicate that the locus of failure of the BN-coated fiber composite occurs at the matrix/BN coating interface.     

The Effects of Surface and Pore Characteristics of Natural Fiber on Interfacial Adhesion of Henequen Fiber/PP Biocomposites

The pore characteristics and morphological changes of henequen fiber after electron beam (EB) irradiation were studied, and their effects on interfacial adhesion between henequen fiber and polypropylene (PP) matrix of biocomposites were investigated. The surface morphologies of the fibers exposed to various EB irradiation doses were observed with an atomic force microscope (AFM). The porosity and pore distribution of fibers were characterized by mercury porosimetry and nonfreezing bound water (NFW) was measured by differential scanning calorimeter (DSC). Henequen fiber-reinforced polypropylene biocomposites were manufactured by the compression molding method and interlaminar shear strength (ILSS) was analyzed to examine the interfacial adhesion between henequen fiber and the PP matrix of the biocomposites. The AFM images indicated that pectin, waxy materials and impurities were removed from the surfaces of the henequen fibers during EB irradiation, resulting in changes of the surface morphology and characteristics of the fibers. When pectin, waxy compounds and impurities were removed, small pores of 1–0.01 μm were produced, and total surface area and porosity were increased. The increase in total surface area and porosity induced better adhesion between fiber and polymer which was confirmed by ILSS tests. However, the excessive creation of small pore size gives a negative effect on the tensile strength of henequen fiber. The best interfacial adhesion between henequen fiber and PP was obtained for the biocomposite reinforced with the henequen fiber treated with 10 kGy, which has the highest surface area and optimum pore diameter for interlocking between henequen fiber and polypropylene.     

Novel Jute/Polycardanol Biocomposites: Effect of Fiber Surface Treatment on Their Properties

In the present study, novel biocomposites with chopped jute fibers and thermosetting polycardanol were prepared using compression molding technique for the first time. Prior to biocomposite fabrication, jute fiber bundles were surface-treated at various concentrations using 3-glycidoxypropyltrimethoxy silane (GPS) and 3-aminopropyltriethoxy silane (APS), respectively. The interfacial shear strength, flexural properties and thermal properties of jute/polycardanol biocomposites reinforced with untreated and silane-treated jute fibers were investigated by means of single fiber microbonding test, three-point flexural test, dynamic mechanical analysis, thermogravimetric analysis and thermomechanical analysis. Both GPS and APS treatments played a role in improving the interfacial adhesion, reflecting that the organofunctional groups located at the end of silane coupling agents may contribute to linking between jute fibers and a polycardanol resin. As a result, it gave rise to increased interfacial shear strength of the biocomposites. Such interfacial improvement also led to increasing the flexural strength and modulus, storage modulus, thermal stability and thermomechanical stability.     

Sorption characteristics of water,oil and diesel in cellulose nanofiber reinforced corn starch resin/ramie fabric composites

Nowadays, utilisation of biodegradable materials has become necessary in order to maintain global environmental and ecological balance. Fully biodegradable nano 'Green' textile composites have been prepared from cellulose nanofibers reinforced corn starch resin and ramie fabric. Nanofibers having dimensions of approximately 1 μm long and 20–30 nm in diameter are used in the study. The nanofibers were incorporated in corn starch resin via ball mill mixing using ceramic balls. Textile composites were fabricated by pasting the reinforced resin onto the ramie fabric and by hot compression molding technique. Interactions at the fiber–matrix interface and the compatibility between cellulose and corn starch resin molecules will affect the properties of the system. The well dispersed cellulose nanofibers contribute higher interfacial area and good fiber networking within the matrix resin. This will lead to better barrier properties. Sorption characteristics of water, oil and diesel in the textile composites were analysed and the influence of nano fibers and macro fibers on the transport phenomena was investigated. The kinetics of sorption-diffusion process was investigated. Kinetic parameters such as n, k, diffusion coefficient, permeability, solubility parameter, % swelling index, etc., were analysed. The presence of cellulose nanofibers influences the sorption mechanism. The water sorption mechanism in the nanocomposites was found to exhibit slight deviation from Fickian mode. Structure–property relationships of the nanocomposites were evaluated.     

Effect of fiber surface treatments on the fiber–matrix interaction in banana fiber reinforced polyester composites

Cellulosic fibers have been used as cost-cutting fillers in plastic industry. Among the various factors, the final performance of the composite materials depends to a large extent on the adhesion between the polymer matrix and the reinforcement and therefore on the quality of the interface. To achieve optimum performance of the end product, sufficient interaction between the matrix resin and the cellulosic material is desired. This is often achieved by surface modification of the resin or the filler. Banana fiber, the cellulosic fibers obtained from the pseudo-stem of banana plant (Musa sepientum) is a bast fiber with relatively good mechanical properties. The fiber surface was modified chemically to bring about improved interfacial interaction between the fiber and the polyester matrix. Various silanes and alkali were used to modify the fiber surface. Modified surfaces were characterized by SEM and FTIR. The polarity parameters of the chemically modified fibers were investigated using the solvatochromic technique. The results were further confirmed by electrokinetic measurements. Chemical modification was found to have a profound effect on the fiber–matrix interactions. The improved fiber–matrix interaction is evident from the enhanced tensile and flexural properties. The lower impact properties of the treated composites compared to the untreated composites further point to the improved fiber–matrix adhesion. In order to know more about the fiber–matrix adhesion, fractured surfaces of the failed composites where further investigated by SEM. Of the various chemical treatments, simple alkali treatment with NaOH of 1% concentration was found to be the most effective. The fiber–matrix interactions were found to be dependent on the polarity of the modified fiber surface.     

Kenaf/polypropylene biocomposites: effects of electron beam irradiation and alkali treatment on kenaf natural fibers

Thermal and dynamic mechanical properties of kenaf natural fiber reinforced polypropylene (PP) biocomposites were examined to compare the effects of natural fiber treatment by electron beam irradiation (EBI) and alkalization. The alpha cellulose contents, the functional groups on the surfaces and the thermal stability of the untreated and treated kenaf fibers were studied. Kenaf fiber/polypropylene(PP) biocomposites were fabricated by means of a compression molding technique using chopped kenaf fibers treated with electron beam (EB) dosages of 100, 200, 500 kGy or with NaOH concentrations of 2, 5, 10 wt%, respectively. The thermal stability, the dynamic mechanical and the interfacial properties of untreated and treated kenaf/PP biocomposites were also investigated through a thermogravimetric analysis, a dynamic mechanical analysis and a fractographic observation, respectively. The results show that the characteristics of kenaf fibers and biocomposites depended on the different treatment level with the EB dosages or on the NaOH concentrations used. In this study, the modification of kenaf fiber surfaces at 200 kGy EBI and treatment with 5 wt% NaOH was most effective for improving the performance of kenaf/PP biocomposites. This study suggests that EBI can be used for modification of natural fiber as an environmentally friendly process and contribute to an improvement in the performances of kenaf/PP biocomposites.     

Predictions of Young's Modulus of Polymer Composites Reinforced with Short Natural Fibers

Polymers reinforced with natural fibers are beneficial to prepare biodegradable composite materials. A new expression for the Young's modulus of short, natural fiber (SNF) reinforced polymer composites was derived based on a micro-mechanical model. The Young's moduli of poly(lactic acid) reinforced with reed fibers and low-density polyethylene (LDPE) reinforced with sisal fibers, from literature data, were estimated in the fiber weight fraction range from 0 to 50% using the equation and both the compounding rule and the Halpin–Tsai equation, and the estimations were compared with the reported measured data. The results showed that the predictions of the Young's moduli by means of the new Young's modulus equation were close to the measured data from the low density polyethylene/sisal fiber composites, as well as the poly(lactic acid)/reed composites at high fiber concentration. Comparing with other Young's modulus equations, the new Young's modulus equation would be more convenient to use owing to the parameters in the equation being easily determined.     

Influence of γ-ray radiation grafting on interfacial properties of aramid fibers and epoxy resin composites

This research used Co⁶⁰ γ-ray radiation to modify Armos fibers in 1,2-epoxy-3-chloropropane. After the treatment, the interlaminar shear strength (ILSS) values of aramid/epoxy composites were improved by about 20%. Surface elements of Armos fibers were determined by XPS analysis, which indicated that the oxygen/carbon ratio was increased. The surface of the fibers treated was rougher than that of the untreated fibers when examined by atomic force microscopy (AFM) and scanning electron microscopy (SEM). Fourier transform infrared (FT-IR) spectra confirmed that the epoxy group was grafted onto the fibers. The wettability of the fibers' surface was also enhanced by the treatment. Nanoindentation technique analysis showed that the nanohardnesses of the various phases (the fiber, the interface and the matrix) in the composite, whose fibers were treated, were correspondingly higher than those in the composite, whose fibers were untreated. The results indicate that γ-ray irradiation grafting technique, which is a suitable batch process for industrialization, can modify the physicochemical properties of Armos fibers and improve the interfacial adhesion of its composite.     

Mechanical,Biodegradation and Morphological Properties of Sisal Fiber Reinforced Poly(Lactic Acid) Biocomposites

Sisal fiber-reinforced poly(lactic acid) (SF/PLA) biocomposites were prepared by melt mixing and subsequent compression molding. The effect of fiber content and sodium hydroxide (NaOH) concentration, used for the fiber mercerization, on the properties of the biocomposites was investigated. It was found that the SFs had a large potential for improving the mechanical properties of the biocomposites. The tensile strength and impact strength increased linearly up to a fiber content of 20%, and then decreased due to the fiber agglomeration. The water absorption was enhanced with increasing the SF content owing to the SFs containing an abundance of hydroxyl groups. The biodegradability of the SF/PLA biocomposites increased similarly. Furthermore, the mercerization led to an increase of the mechanical properties of the biocomposites, which normally depended on the fiber-matrix adhesion. The mercerization had competing effects on the water absorption and biodegradability, including not only the positive function of the improved hydrophilicity of the mercerized-SF but also the negative role of the increase of fiber-matrix interfacial adhesion. Overall, the optimum SF load for mechanical properties was 20?wt% due to a good balance between the reinforcement and distribution of the SFs, whereas the 6% NaOH concentration was optimal owing to the resulting fibers yielding the highest mechanical properties and acceptable water resistance and biodegradability.     

Characterization of Interfacial Stress Transfer Ability by Dynamic Mechanical Analysis of Cellulose Fiber Based Composite Materials

The stress transfer ability at the fiber–matrix interface of wood fiber composites is known to affect the mechanical properties of the composite. The evaluation of interface properties at the level of individual fibers is however difficult due to the small dimensions and variability of the fibers. The dynamical mechanical properties of composite and constituents, in this case wood fibers and polylactide matrix, was here used together with micromechanical modeling to quantify the stress transfer efficiency at the fiber–matrix interface. To illustrate the methodology, a parameter quantifying the degree of imperfection at the interface was identified by inverse modeling using a micromechanical viscoelastic general self-consistent model with an imperfect interface together with laminate analogy on the composite level. The effect of moisture was assessed by comparison with experimental data from dynamic mechanical analysis in dry and moist state. For the wood fiber reinforced polylactide, the model shows that moisture absorption led to softening and mechanical dissipation in the hydrophilic wood fibers and biothermoplastic matrix, rather than loss of interfacial stress transfer ability.     

Relation between interfacial shear strength and compressive strength of carbon fiber/epoxy resin composite strands

The mechanism with which the fiber-matrix interfacial strength exerts its influence on the compressive strength of fiber reinforced composites has been studied by measuring the axial compressive strength of carbon fiber/epoxy resin unidirectional composite strands having different levels of interfacial shear strength. The composite strands are used for experiments in order to investigate the compressive strength which is not affected by the delamination taking place at a weak interlayer of the laminated composites. The interfacial strength is varied by applying various degrees of liquid-phase surface treatment to the fibers. The efficiency of the compressive strength of the fibers utilized in the strength of the composite strands is estimated by measuring the compressive strength of the single carbon filaments with a micro-compression test. The compressive strength of the composite strands does not increase monotonically with increasing interfacial shear strength but showes lower values at higher interfacial shear strengths. With increasing interfacial shear strength, the suppression of the interfacial failure in the misaligned fiber region increases the compressive strength, while at higher interfacial shear strengths, the enhancement of the crack sensitivity decreases the compressive strength.     

Micromechanical Behavior of Carbon Nanotube-Covered SiC Fibers in Polymer Matrix Composites

The incorporation of nanotube-covered fibers in continuous fiber/epoxy composites has been shown to influence the mechanical, electrical, and thermal properties of the composite. Increased interlaminar shear stress, flexural strength and modulus have been reported in such composites over composites containing bare fibers. In this study, the microstructure and interfacial shear strength (ISS) of continuous silicon carbide fiber/epoxy composites with and without nanotubes grown from the SiC fiber surface were investigated with micro-Raman spectroscopy (MRS) and microscopy. The fibers with nanotubes grown from the surface were found to have a reduced ISS compared with the bare fibers. Electron microscopy showed good wetting of epoxy in the nanotube forests, but poor attachment of the nanotube forests to the fibers. These results suggest that the mechanism leading to improvements in bulk composite properties is not due to an improvement in the fiber/matrix ISS.     

In situ observation of interfacial debonding process induced by matrix crack propagation in two-dimensional unidirectional model composites

Interfacial debonding behavior is studied for unidirectional fiber reinforced composites from both experimental and analytical viewpoints. A new type of two-dimensional unidirectional model composite is prepared using 10 boron fibers and transparent epoxy resin with two levels of interfacial strength. In situ observation of the internal mesoscopic fracture process is carried out using the single edge notched specimen under static loading. The matrix crack propagation, the interfacial debonding growth and the interaction between them are directly observed in detail. As a result, the interfacial debonding is clearly accelerated in specimens with weakly bonded fibers in comparison with those with strongly bonded fibers. Secondary, three-dimensional finite element analysis is carried out in order to reproduce the interfacial debonding behavior. The experimentally observed relation between the mesoscopic fracture process and the applied load is given as the boundary condition. We successfully evaluate the mode II interfacial debonding toughness and the effect of interfacial frictional shear stress on the apparent mode II energy release rate separately by employing the present model composite in combination with the finite element analysis. The true mode II interfacial debonding toughness for weaker interface is about 0.4 times as high as that for a stronger interface. The effect of the interfacial frictional shear stress on the apparent mode II energy release rate for the weak interface is about 0.07 times as high as that for the strong interface. The interfacial frictional shear stress and the coefficient of friction for weak interface are calculated as 0.25 and 0.4 times as high as those for strong interface, respectively.     

Influence of material processing and interface on the fiber fragmentation process in titanium matrix composites

The objective of this work is to study the effect of composite processing conditions on the nature of the fiber–matrix interface in titanium matrix composites and the resulting fragmentation behavior of the fiber. Titanium matrix, single fiber composites (SFCs) were fabricated by diffusion bonding and tensile tested along the fiber axis to determine their interfacial load transfer characteristics and the resulting fiber fragmentation behavior. Two different titanium alloys, Ti-6Al-4V (wt%) and Ti-14Al-21Nb (wt%), were used as matrix material with SiC (SCS-6) fibers as reinforcement. The tensile tests were conducted at ambient temperature and were continuously monitored by acoustic emission. It was observed that the Ti-6Al-4V/SCS-6 composite system exhibited a greater degree of fiber–matrix interfacial reaction, as well as a rougher interface, compared to Ti-14Al-21Nb/SCS-6 composites. Acoustic emissions during tensile testing showed that most of the fiber fractures in Ti-6Al-4V/SCS-6 occurred at strains below ～5% and the fragmentation ceased at ～10% strain corresponding to specimen necking. In contrast, the Ti-14Al-21Nb/SCS-6 composite deformed without necking and fiber fractures occurred throughout the plastic range until final fracture of the specimen at about 12% strain. The markedly different fragmentation characteristics of these two composites were attributed to differences in the fiber–matrix interfacial regions and matrix deformation behavior.     

Preparation,Properties and Applications of Chitosan-Based Biocomposites/Blend Materials: A Review

Taking inspiration from many published chitosan (Cs)-based biocomposites, this article is written to highlight the significant effect of reinforcing and/or blending Cs polymer with the different constituents to increase various properties (mechanical, hydrophilic, thermal, adsorption ability and stability) of Cs without sacrificing any of its positive properties. It is concluded that the properties of Cs biocomposites with a synthetic constituent have contributed to its rigidity since only mechanical interaction occurred at the interfacial region. Instead of physical interactions, the addition of an organic constituent also promoted the chemical interactions at the interfacial region of the Cs biocomposites. This consequently produced Cs biocomposites with synthetic constituents with relatively low strength and stiffness but high resistance to fracture, whereas the ones with an organic constituent have high strength and stiffness but are very brittle. This review also screens the current applications of Cs-based biocomposites in the field of drug delivery, tissue engineering, antibacterial, food packaging, biomedical, metal adsorption and dye removal.     

Effect of chemical treatment on dynamic mechanical properties of sisal fiber-reinforced polyester composites fabricated by resin transfer molding

The dynamic mechanical properties of treated sisal fiber-reinforced polyester composites fabricated by resin transfer molding (RTM) have been studied with reference to fiber surface modifications, frequency and temperature. The sisal fibers have been subjected to various chemical and physical treatments like mercerization, heating at 100°C, permanganate, benzoylation and vinyl tris(2-ethoxymethoxy) silane to improve the interfacial bonding with isophthalic polyester resin. Results indicated that treatment changed the storage modulus (E′), loss modulus (E″) and damping factor (tan δ) drastically at a wide range of temperature. The E′ value increased for every treatment, and is maximum for the composites fabricated by benzoylated-treated fibers. The T _g value obtained from the E″value showed an increase as compared to untreated fiber-reinforced composites. The alkali-treated fiber-reinforced composites showed lower tan δ value. Using Arrhenius' equation the activation energy was calculated and found maximum for the composites fabricated by alkali-treated fiber, which shows good fiber/matrix interactions.     

Upgrading poly(butylene succinate)/wood fiber composites by esterified lignin

Aliphatic chains were introduced into the macromolecule of kraft lignin using aliphatic chlorides as esterification reagents. The hydrophobicity of esterified lignin (EL) was enhanced as compared to the original lignin. EL was further used as a macromolecular coupling agent in poly(butylene succinate)/chemi-thermomechanical pulp fiber composites. As a result, the composites with enhanced mechanical performance were obtained, and the tensile strength, impact strength, and bending strength were increased by 25.1, 22.4, and 19.3%, respectively, under 2 wt% EL-treatment (synthesized by palmitoyl chloride, –COCl/–OH = 1.5:1) in comparison with those of the specimen without any coupling agent treatment. Furthermore, the composite prepared with EL-treated fibers shows significant lower water absorption ratio than that of untreated one. A significant increase in storage modulus (E′) was observed upon the incorporation of treated fibers. Furthermore, the improved interfacial bonding between treated fibers and matrix was verified by SEM images. The shear viscosity of composite was increased by the incorporation of EL, but in general, the rheological behaviors of composites are not significantly changed.     

Effect of silane/nano-silica on the mechanical properties of basalt fiber reinforced epoxy composites

The present study explains the role of surface modification of constituent materials on composite material performance. The influence of silane and nano-hybrid coatings on mechanical properties of basalt fibers and composite materials on their base was investigated. Infrared spectroscopy indicated that modification of basalt fiber surface and nano-SiO₂ was successfully applied. The surface modification leads to the significant increase in the tensile strength of basalt fibers compared to the non-coated fibers. The tensile strength of silane-treated fibers was established 23% higher than the non-coated fibers, indicating that silane plays a critical role in the strength retention of basalt fibers. Also it was pointed out that silane coupling agents can be used for the preparation of the nano-hybrid coating. Addition of SiO₂ nanoparticles into the fiber surface was incorporated to enhance the interfacial bonding of basalt fiber reinforced epoxy composite.