Natural fiber blend—nylon 6 composites

In this study, engineering thermoplastic composites were prepared from natural fiber blend–filled nylon 6. Natural fiber blend from a mixture of kenaf, flax, and hemp fibers were added to nylon 6 using melt mixing to produce compounded pellets. The natural fibers/ nylon6 composites with varying concentrations of natural fibers (from 5 to 20 wt%) were prepared by injection molding. The tensile and flexural properties of the nylon 6 composites were increased significantly with the addition of the natural fiber blend. The maximum strength and modulus of elasticity for the nylon 6 composites were achieved at a natural fiber blend weight fraction of 20%. The Izod impact strength of composites decreased with the incorporation of natural fibers without any surface treatments and coupling agent. The melt flow index (MFI) also decreased with increasing natural fiber blend loading. The results of tensile and flexural modulus of elasticity (FMOE) are in accordance with the rheological data from the MFI measurements. The increase in the tensile and flexural properties indicated that efficient bonding occurred between the natural fibers and nylon 6. No fiber pullout was observed during the scanning electron microscopic analysis of the fracture surfaces. The higher mechanical results with lower density demonstrate that a natural fiber blend can be used as a sufficient reinforcing material for low‐cost, eco‐friendly composites in the automotive industry and in other applications such as the building and construction industries, packaging, consumer products, etc.POLYM. COMPOS., 2013. © 2013 Society of Plastics Engineers     

Effects of raw fiber materials,fiber content,and coupling agent content on selected properties of polyethylene/wood fiber composites

This study investigated the effects of raw fiber materials, fiber content, and coupling agent (CA) content on mixing torque, rheological properties, and crystallization behavior of wood plastic composites (WPC). WPCs were prepared through melt molding processes. This study adopted a response surface strategy of 20 run optimal design for three factors including wood fiber type, fiber content, and CA content. Wood fiber type or wood fiber characteristics influence equilibrium torque and viscosity. The power index n for viscosity as a function of frequency was affected not only by wood fiber content, but also by CA content and wood fiber type. Addition of wood fibers to the system as nucleating agents favors polyethylene crystallization. The values of crystallization enthalpy and melt enthalpy were correlated with wood fiber content and CA content, but they were not affected by wood fiber type. The melt temperatures of polyethylene and composites were comparable. This indicates that the crystallite structure and lamellar thickness are similar. POLYM. ENG. SCI., 47:1678–1687, 2007. © 2007 Society of Plastics Engineers     

Molding of PBO fabric reinforced thermoplastic composite to achieve high fiber volume fraction

In fiber‐reinforced plastic materials, the fiber volume fraction is one of the most important parameters, and it strongly influences the composite properties. However, it is hard to improve impregnation and the fiber volume fraction in fiber‐reinforced thermoplastics because thermoplastic resins have high melt viscosities. This study explored a reformative solution impregnation method for molding fabric‐reinforced thermoplastic composites with a high fiber volume fraction. The fiber volume fraction was significantly increased, to 60%, which is equal to that of fiber‐reinforced thermosetting plastic materials. A comparison indicated that a fiber‐reinforced thermoplastic and a fiber‐reinforced thermosetting plastic with the same reinforcing fiber had similar tensile properties and that the proposed molding method is effective in thermoplastic composite manufacture. POLYM. COMPOS., 34:953–958, 2013. © 2013 Society of Plastics Engineers     

Thermotropic polyester amide-carbon fiber composites

Liquid crystal polymers (LCP) have been developed for the first time as a thermoplastic matrix for high-performance composites. A successful melt impregnation method has been developed that results in the production of continuous carbon fiber (CF)-reinforced LCP prepreg tape. Subsequent layup and molding of prepreg into laminates has yielded composites of good quality. Tensile and flexural properties of LCP-CF composites are comparable to those of epoxy-CF composites. LCP-CF composites have better impact resistance than the latter, although epoxy-CF composites possess superior compression and shear strength. LCP-CF composites have good property retention until 200°F (67% of room temperature value). Above 200°F, mechanical properties are found to decrease significantly. Experimental results indicate that the poor compression and shear strength may be due to the poor interfacial adhesion between the matrix and carbon fiber.     

New hybrid method for simultaneous improvement of tensile and impact properties of carbon fiber reinforced composites

For weight savings of automobiles to improve fuel efficiency, tensile and impact strengths of carbon fiber reinforced composites (CFRC) are important properties required for substitution of metallic or ceramic automotive parts by CFRC parts. Effect of surface treatments of carbon fiber (CF) such as plasma, nitric acid, and liquid nitrogen treatments on interfacial bonding and mechanical properties of CF reinforced thermoplastic composites was investigated and nitric acid treatment was the best method to improve the interfacial affinity between the used CF and thermoplastic polymer matrix since the treatment induced acidic functional groups on the surface and increased surface roughness simultaneously. A new hybrid fabrication method was suggested by applying a bi-component two-layer structure to the film insert molding to improve tensile and impact strengths of CFRC simultaneously. Compared with tensile and impact strengths of the base polymer, those of the new hybrid composites filled with rubber particles and CF were improved by about 41.3% and 105.7%, respectively. In particular, tensile and impact strengths of the composite specimen prepared by the hybrid fabrication method were improved by about 15.0% and 36.0%, respectively when compared with those of the composite specimen prepared by the conventional melt mixing.     

Effects of processing variables on the mechanical properties of compression molded polystyrene-wood fiber composites

Optimization of mixing and molding conditions (e.g. temperature, time and pressure) of aspen chemithermomechanical pulp (CTMP)-polystyrene composites was carried out. Compounding conditions showed a substantial effect on the mechanical properties of the composites. The effect of fiber encapsulation with polystyrene on the mechanical properties of the composites was also evaluated. Compared to non-encapsulated ones, the mechanical properties of composites showed superior results when encapsulated CTMP fibers were used. After encapsulation of wood fibers, and optimization of mixing and molding conditions, composites with up to 36% of fiber volume fraction could be incorporated in polystyrene with improved mechanical properties.     

Design of a vane mixer with controlled extensional/shear strength ratio and its application for carbon fiber/polyamide 6 composites

In this work, a novel melt mixing method and its corresponding mixing device are developed. The extensional/shear strength ratio of the device can be controlled by adjusting its eccentricity. The structure and working principle of the device are introduced in detail. Carbon fiber (CF)/polyamide 6 (PA6) composites are prepared via this novel mixing device. The influences of eccentricity and mixing time on the morphology, CF length, thermal, mechanical, and electrical properties of CF/PA6 composites are studied. Scanning electron microscopy results show that CFs uniformly disperse in the matrix and interfacial adhesion between CFs and PA6 is improved. It is observed that CF length and its distributions can be optimized by changing eccentricity. The maximum average fiber length is about 351 μm. Differential scanning calorimetry results exhibit that the X_c increases 6.5% when eccentricity is 2 mm. Mechanical test results show tensile strength and modulus increase first and then decrease with the increasing eccentricities or mixing time. Electrical property measurement shows an obvious increase when eccentricity is 2 mm due to good fiber dispersion and long fiber retention length. The experimental results indicate that the novel mixing method and its corresponding apparatus provide an environment-friendly and effective way to prepare polymer-based composites.     

Approaches to improve the properties of wood fiber reinforced cementitious composites

In an attempt to improve the workability, stability, and physical and mechanical properties of wood fiber-reinforced cementitious composites (WFRCs), alkali-activated blended cements have been explored for their compatibility with various wood fibers such as hardwood fiber, recycled newspaper fiber and recycled kraft paper fiber. Methods including high shear mixing, modifying the cement matrix with silica fume, and molding pressure were evaluated as means for further strengthening the wood fiber-reinforced cement composites. Flexural strengths up to 40 MPa. along with enhanced toughness have been achieved.     

Structural properties and mechanical behavior of injection molded composites of polypropylene and sisal fiber

Composites based on isotactic polypropylene (PP) and sisal fiber (SF) were prepared by melt mixing and injection molding. The melt mixing characteristics, thermal properties, morphology, crystalline structure, and mechanical behavior of the PP/SF composites were systematically investigated. The results show that the PP/SF composites can be melt mixed and injection molded under similar conditions as the PP homo‐polymer. For the composites with low sisal fiber content, the fibers act as sites for the nucleation of PP spherulites, and accelerate the crystallization rate and enhance the degree of crystallinity of PP. On the other hand, when the sisal fiber content is high, the fibers hinder the molecular chain motion of PP, and retard the crystallization. The inclusion of sisal fiber induces the formation of β‐form PP crystals in the PP/SF composites and produces little change in the inter‐planar spacing corresponding to the various diffraction peaks of PP. The apparent crystal size as indicated by the several diffraction peaks such as L_(110)α, L_(040)α, L_(130)α and L_(300)β of the α and β‐form crystals tend to increase in the PP/SF composites considerably. These results lead to the increase in the melting temperature of PP. Moreover, the stiffness of the PP/SF composites is improved by the addition of sisal fibers, but their tensile strength decreases because of the poor interfacial bonding. The PP/SF composites are toughened by the sisal fibers due to the formation of β‐form PP crystals and the pull‐out of sisal fibers from the PP matrix, both factors retard crack growth.     

Asphaltene/polymer composites: Morphology,compatibility, and rheological properties

In this study, we investigate the use of asphaltene, a natural waste product that is inevitably formed during heavy oil processing, as a filler in polymer composites. The focus of this work is on the compatibility of various asphaltenes, featuring different polarities, with several polymers, including polypropylene (PP), polystyrene (PS), polymethyl methacrylate (PMMA), and polycarbonate (PC). The Hansen solubility parameters were plotted to predict the compatibility of polymers with different asphaltenes. Then, polymer composites were prepared by two common techniques: melt mixing and solution mixing. The dispersion state of the asphaltenes in each polymer was investigated by using imaging and rheological techniques. This work showed that the network structure of the asphaltenes and, thus, the final properties of the composites can be controlled by the polarity of asphaltenes, mixing technique, and melt viscosity of the polymer. For instance, more polar asphaltene (Asph P) produced smaller aggregates in PMMA, which has a higher polar solubility parameter than PP or PS. At 2.5 wt.% of asphaltene, Asph P showed 26% and 177% larger asphaltene agglomerates in PP and PS, respectively, than the less polar asphaltene (Asph Al). PS/asphaltene and PMMA/asphaltene composites prepared by the solution mixing method exhibited better dispersion compared to their melt-mixed counterparts. In melt-mixed composites, the dispersion quality of the asphaltene was better for polymers with higher melt viscosity. Thus, a careful choice of polymer, asphaltene, and preparation conditions can be used to tune the properties of asphaltene/polymer composites.     

Preparation and characterization of LDPE and PP—Wood fiber composites

Natural fiber reinforced composites is an emerging area in polymer science. These natural fibers are low cost fibers with low density and high specific properties. These are biodegradable and nonabrasive. The natural fiber composites offer specific properties comparable to those of conventional fiber composites. However, in development of these composites, the incompatibility of the fibers and poor resistance to moisture often reduce the potential of natural fibers, and these draw backs become critical issue. Wood‐plastic composites (WPC) are a relatively new class of materials and one of the fastest growing sectors in the wood composites industry. Composites of wood in a thermoplastic matrix (wood–plastic composites) are considered a low maintenance solution to using wood in outdoor applications. WPCs are normally made from a mixture of wood fiber, thermoplastic, and small amounts of process and property modifiers through an extrusion process. In this study, Wood–plastic composites (WPC) are produce by adding a maleic anhydride modified low density polyethylene coupling agent to improve interfacial adhesion between the wood fiber and the plastic. Mixing is done with twin screw extruder. Subsequently, tensile strength, the modulus of elasticity, % elongation, hardness, Izod impact strength, melt flow index (MFI), and heat deflection temperature (HDT) are determined. Thermal transition temperatures and microstructure are determined with DSC and SEM, respectively. © 2009 Wiley Periodicals, Inc. J Appl Polym Sci, 2009     

Effect of flax fiber content on polylactic acid (PLA) crystallization in PLA/flax fiber composites

Crystallization of polylactic acid (PLA) has a profound effect on its thermal stability and mechanical properties. However, almost no crystallization occurs in actual injection molding process due to rapid cooling program. In this paper, flax fiber was employed as nucleator to enhance the crystallization capability of PLA. Effects of flax fiber content on cold crystallization, melt crystallization, crystallinity, crystal form, morphologies, and size of spherulites of PLA/flax fiber composites were investigated. Dynamic mechanical analysis was innovatively employed to study cold crystallization temperature of PLA/flax fiber composites under dynamic force, and the relationship between cold crystallization temperature (y) and flax fiber content (x) data was fitted by the function y = 34.1 × exp (?x/5.7) + 78.0. The differential scanning calorimetry results showed that the cold crystallization temperature of composites dropped, the melt crystallization temperature of composites increased, and the crystallinity of composites improved with increasing of flax fiber content. Using polarized optical microscopy, it has been found that the spherocrystal size of composites was much smaller than that of neat PLA, and flax fiber induced transcrystallization on the flax fiber surfaces. Wide-angle X-ray diffraction was applied to reveal that flax fiber significantly enhanced the formation of α-form PLA crystals.     

Manufacturing and testing of long basalt fiber reinforced thermoplastic matrix composites

In this work, long basalt fiber reinforced composites were investigated and compared with short basalt fiber reinforced compounds. The results show that long fiber reinforced thermoplastic composites are particularly advantageous in the respects of dynamic mechanical properties and injection molding shrinkage. The fiber orientation in long basalt fiber reinforced products fundamentally differs from short basalt fiber reinforced ones. This results in more isotropic molding shrinkage in case of long basalt fiber reinforced composites. The main advantage of the used long fiber thermoplastic technology is that the special long fiber reinforced pellet can be processed by most conventional injection molding machines. During extrusion compounding the fibers in the compound containing 30 wt% fibers are fragmented to an average length of 0.48 mm (typical of short fiber reinforced thermoplastic compounds), this length decreases further during injection molding to 0.20 mm. Contrarily using long fiber reinforced pellets and cautious injection molding parameters, an average fiber length of 1.8 mm can be achieved with a conventional injection molding machine, which increased the average length/diameter ratio from 14 to 130. POLYM. ENG. SCI., 2010. © 2010 Society of Plastics Engineers     

Studies on mechanical properties of sisal fiber/phenol formaldehyde resin in‐situ composites

Phenol formaldehyde resin (PF) reinforced with short sisal fibers (SF) were obtained by two methods, direct‐mixing and polymerization filling. Impact and bending properties of resulting composites were compared. Under the same compression molding conditions, polymerization filled composites showed better mechanical properties than those of direct‐mixed composites. The influences of fiber modifications on the mechanical properties of SF/PF in‐situ (polymerization filled) composites have been investigated. Treated‐SF‐reinforced composites have better mechanical properties than those of untreated‐SF‐reinforced composites. The effects of SF on water absorption tendencies of SF/PF composites have also been studied. In addition, sisal/glass (SF/GF) hybrid PF composites of alkali‐treated SF were prepared. Scanning electron microscopic studies were carried out to study the fiber‐matrix adhesion. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Effect of kenaf fiber age on PLLA composite properties

A challenge facing engineering with natural fibers is the high standard deviation of mechanical properties of natural fiber compared with synthetic fiber. Plants have a chemical and physical architecture reflective of their age. The region near the apex is more flexible than that near the base. In this paper we investigate the impact of increasing age of plant fiber on the corresponding composite. Bast fibers stems of kenaf (Hibiscus cannabinus, L.), a warm season tropical herbaceous annual plant extracted corresponding to different age, were dispersed into Poly‐l ‐lactide (PLLA) matrix by melt blending followed by compression molding. The resulting bio‐based hybrid composites were characterized by X‐ray diffraction (XRD), attenuated total reflectance‐Fourier transfer infrared spectroscopy (ATR‐FTIR), differential scanning calorimetry (DSC), optical microscopy (OM), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA) were conducted. DSC and XRD indicated that the kenaf was effective in promoting crystallization. TGA indicated that the thermal stability of composites is reduced compared with PLLA, but the older fiber sample based on 120–150 cm from the plant apex improved thermal stability compared with the rest. SEM and OM inferred good fiber dispersion while dynamic mechanical tests revealed increased modulus. POLYM. COMPOS., 35:915–924, 2014. © 2013 Society of Plastics Engineers     

Thermal and dielectric properties of fiber reinforced polystyrene composites

Thermal and dielectric properties of polymer composites are important for many applications such as microelectronic packaging. In this work, glass fiber, alumina fiber, and carbon fiber reinforced polystyrene composites have been prepared with melt blending. The thermal conductivity, thermal expansion, and dielectric properties of the composites have been systematically studied as a function of fiber fraction. It is found that all the three types of the fibers, particularly the carbon fiber, can significantly increase the thermal conductivity and decrease the thermal expansion of the polymer. Moreover, the incorporation of the glass or alumina fibers does not have obviously adverse effect on the dielectric constant of the polymer. The thermal conductivities of the fibers reinforced composites have also been analyzed with Agari's model to reveal the conductive enhancement nature of the fibers to the polymer. POLYM. COMPOS., 2008. © 2008 Society of Plastics Engineers     

Polypropylene–glass fiber/basalt fiber hybrid composites fabricated by direct fiber feeding injection molding process

Hybrid composites of polypropylene reinforced with glass fibers and basalt fibers were fabricated by vented injection molding machine which is named the direct fiber feeding injection molding (DFFIM) process. Polyamide 6 and maleic anhydride‐grafted polypropylene has been used as a coupling agent to improve the interfacial bonding between the fibers and matrix. Two types of vented injection molding machines with a different check ring and mold were used for making specimens. The fiber lengths were analyzed to identify the most suitable check ring and mold for the DFFIM process. The mechanical properties of the hybrid composites were investigated by tensile, flexural and Izod impact tests. The interfacial morphology of the fractured tensile specimens was studied by using scanning electron microscopy and showed that there is a fiber agglomeration phenomenon that occurs in the hybrid composites, and it has a significant effect on the mechanical properties of hybrid composites. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017 , 134, 45472.     

Mechanical properties of natural fibers/polyamides composites

The aim of this investigation has been to use high performance thermoplastic matrices such as polyamides instead of the commonly used polyolefins to develop natural fiber composites for substituting glass fibers without renouncing to their mechanical properties. For this purpose, different natural fibers such as flax, jute, pure cellulose, and wood pulps have been melt compounded with different polyamides to analyze the effect of fiber content on mechanical properties. Fibers have not been treated as polyamides are less hydrophobic than polyolefins. Thermal behavior of the different fibers was determined by thermogravimetry to know the boundary for processing at high temperatures, since the melting points of the polyamides are much higher than those of polyolefins and this could lead to a higher degradation of the natural fibers. Rheological parameters were deduced by measuring torque values during the mixing process. Flexural and tensile modulus and strength of composites were analyzed, finding an increase in the mechanical properties compared with the unreinforced matrix that turns natural fibers into a considerable reinforcement offering a wealth of possibilities for industrial applications. POLYM. COMPOS., 2009. © 2008 Society of Plastics Engineers     

Mechanical and viscoelastic properties of short fiber reinforced natural rubber composites: effects of interfacial adhesion,fiber loading,and orientation

The effect of a two-component dry bonding system consisting of resorcinol and hexamethylene tetramine on the mechanical and viscoelastic properties of short sisal fiber reinforced natural rubber composites has been studied. The studies were conducted with chemically treated and untreated short sisal fibers. Treated fibers impart better mechanical properties to the composites. By mixing with short fibers, the dynamic storage modulus (E') of natural rubber composites was improved. The effects of fiber-matrix adhesion on the mechanical and viscoelastic properties of the composites were investigated. The storage moduli and mechanical loss increased continuously with an increase in fiber loading but decreased with an increase of temperature. The influence of the fiber orientation on the mechanical and viscoelastic properties is discussed.     

Recyclability of a glass fiber poly(butylene terephthalate) composite

The recyclability of a fiber-reinforced poly(butylene terephthalate) (PET) composite has been studied. After treatment with a suitable silane, processed regrind composites are successfully recycled, with mechanical properties as good as a comparable, commercial composite. The three processing techniques investigated are injection molding, extrusion compression molding and compression molding. As expected, processing technique and processing parameters are important in determining the mechanical properties of the molded regrind. Our results show that injection- and extrusion-compression-molded regrind composites have good fiber bundle dispersion and fiber alignment, resulting in tensile properties better than the compression-molded samples. On the other hand, compression-molded samples, which show random fiber orientation and low fiber bundle dispersion, have lower tensile properties, but better impact strength than injection- and extrusioncompression-molded composites.